diff --git "a/Botany/a_handbook_of_systematic_botany_1904.md" "b/Botany/a_handbook_of_systematic_botany_1904.md" new file mode 100644--- /dev/null +++ "b/Botany/a_handbook_of_systematic_botany_1904.md" @@ -0,0 +1,25947 @@ +barcode 9780500691313 + +___-___-___ + +[API_EMPTY_RESPONSE] + +10 + +A HANDBOOK +OF +SYSTEMATIC BOTANY + +Some Opinions of the Press on +Warming's "Systematic Botany." + +"A very complete, systematic classification of plants, with all their principal characteristics. It is a book well worth reading, and is well printed and illustrated."—*Lancet.* + +"As a text book of Botany this will take a high place, and as a handbook of reference it will prove valuable. The volume is well adapted to the use of the beginner, and a very serviceable text book for students."—*Knowledge.* + +"Professor Warming's contribution to morphology and systematic botany are highly valued by botanical workers, who will find in this work a valuable supplement to the *Systema Vegetabilium*. We commend the book to the notice of those who require to obtain a good general knowledge of the application of morphology to purposes of classification."—*Cassell.* + +"It has been well translated, and will be found a useful and trustworthy handbook."—*Journal of Education.* + +"Mr. Potter has done English students of botany a great service in giving them an excellent translation of Dr. Warming's important work."—*Educational Review.* + +Botany + +A HANDBOOK OF SYSTEMATIC BOTANY + +BY +DR. E. WARMING +Professor of Botany in the University of Copenhagen + +WITH A REVISION OF THE FUNGI BY +DR. E. KNOBLAUCH, +Karlsruhe + +TRANSLATED AND EDITED BY +M. C. POTTER, M.A. F.L.S. +Professor of Botany in the University of Durham +College of Science, Newcastle-upon-Tyne +Author of "An Elementary Textbook of Agricultural Botany" + +WITH 610 ILLUSTRATIONS + +A black and white illustration of a plant with a label "LONDON" on it. +London + +SWAN SONNENSchein & CO. LIM +NEW YORK : THE MACMILLAN CO +1904 + +84642 +15-11-07 + +FIRST EDITION, MARCH 1894 ; SECOND EDITION, JULY 1904 + +PREFACE. + +The present translation of Dr. E. Warming's *Hansæ Bog* i den Systematiske Botanik is taken from the text of the 3rd Danish Edition (1892), and from Dr. Knoblauch's German Edition (1880), and the book has been further enriched by numerous additional notes which have been kindly sent to me by the author. Dr. Warming's work has long been recognised as its original and important contribution to Systematic Botany, and I have only to regret that the presence of other scientific duties has delayed its presentation to English readers. Dr. Warming desires me to record his high appreciation of the careful translation of Dr. Knoblauch, and his obligation to him for a number of corrections and improvements of which he has made use in the 3rd Danish Edition. In a few instances I have made slight additions to the text; these, however, appear as footnotes, or are enclosed in square brackets. + +In this present Edition the Thallophytes have been revised and rearranged from notes engulfed to me by Dr. Knoblauch, to whom I am indebted for the Classification of the Fungi, according to the more recent investigations of Brefeld. The Bacteria have been revised by Dr. Mignola, the Florae rearranged after Schmitz, and the Taphrinoceae after Sadebeck. The main body of the text of the Algae and Fungi remains as it was originally written by Dr. Wille and Dr. Rostrup in the Danish Edition, though in many places considerable alterations and additions have been made. For the most part my additions are due to the classification adopted in the Danish Edition is given in the Appendix. + +In the Angiospermae I have retained the sequence of orders in the Danish original, and have not rearranged them according to w. e. +*e* + +vi +PULPACE. + +the systems more familiar to English students. In any rearrangement much of the significance of Dr. Warming's valuable and original observations would have been lost, and also from a teacher's point of view I have found this system of great value. +Although at present it may not be completely satisfactory, yet as the attention has been called to the fact that the advance and regression of many of the orders, it may be considered to have a distinct advantage over the new artificial systems founded upon Jussieu's Divisions of Polypetalea, Gamopetalea, and Apatalea. + +With reference to the principles of the systematic arrangement adopted, I may here insert the following brief communication from the author (dated March, 1850), which he has requested me to quote, in order to show the progress made in this work. Each form, which, on comparative morphological considerations, is clearly less simple, or can be shown to have arisen by reduction or through abortion of another type having the same fundamental structure, or in which a further differentiation and division of labour is found, will be regarded as younger, and as far as possible, and so far as other considerations will admit, will be reviewed later than the 'simple', more complete, or richer forms. +For instance, to serve as an illustration: Eriocaulon and Potamogeton are seen to be derived from the Epiphyllum Symphytonia. Chloro- +petalea, Monocotyledonea are, therefore, treated last; the Hydro- +charitaceae are considered last under the Helobaeae, etc. Zygophyophyta is younger than Astrocarpoïdeæ; the Selimiaceae and Gymnandraceae therefore follow after the Liliiferae; the Spermatophytae after the Solanaceae; Lirariaceae after Verbascumae, etc. Forms with united leaves indicate younger types than those with free leaves; hence the Symptomeae after the Characteae; the Sileneae after the Alliaceae; the Muscaceae after the Solanaceae; etc., etc. + +*Actuelis* (spiral-leaved) forms are older than cyclical (verticillate-leaved) with a definite number, comparing, of course, only those with the same fundamental structure. The Veronicace-type must be considered as younger, for example, than Digitalis and *Antir- + +PREFACE. + +vii + +**Rhiisum,** these again as younger than **Sereophularia; Verbascon,** on the contrary, is the least reduced, and therefore considered as the oldest form. Similarly the one-seeded, nut-fruited **Rosanfacios** are considered as a later type (with evident abortion) than the many-seeded, foliolar forms of the Order; the **Paroogaeon** and **Corynothec** being intermediate between them. Moreover, this occurrence of few seeds in an ovary as generally arising through reduction of the many-seeded forms. The **Oopertus** are regarded as a form derived from the Juncaceae through reduction, and associated with this, as so often the case, there is a complication of the inflorescence; the **Dipanaceae** are again regarded as a form proceeding from the Valerianaceae by a similar reduction, and those in their turn as an off-shoot from the **Caprifolideae**, etc. Of course these principles of systematic arrangement could only be applied to plants, for breeding purposes they have often required modification. + +In preparing the translation considerable difficulty has been experienced in finding a satisfactory rendering of several terms which have no exact equivalent in English. I may here especially mention the term *Verbalt* (Forb.) which I have translated by the term *bracteole*, when it clearly applied to the first leaf (or leaves) on a podicel; but in discussing questions of general morphology a term was much needed to include both vegetative and reproductive parts of the plant, and I have adopted "Floral-leaf." Also, the term "Floral-leaf" has been adopted as an equivalent of "Hochblatt," and the term "bract" has been limited to a leaf subtending a flower. + +At the end of the book will be found a short appendix giving an outline of some of the earlier systems of Classification, with a more complete account of that of Hooker and Bentham. + +In a book of this character it is almost impossible to avoid some errors, but it is hoped that these will be comparatively few. In connection with this work I have received valuable assistance from Dr. Warming and Dr. Knoblauch, who have kindly read through each sheet, and to whom I am greatly indebted for + +viii +PREFACE. + +many criticisms and suggestions. I have also to thank Mr. I. H. Barkill for his kind assistance in looking over the proofs of the Monocotyledons and Dicotyledons, and Mr. Harold Wager for kindly reading through the proofs of the Algae and Fungi. My thanks are also especially due to Mr. E. L. Danielsen, and I wish to take this opportunity of acknowledging the very considerable help which I have received from him in translating from the Original Danish. + +M. C. POTTER. + +January, 1893. + +TABLE OF CONTENTS. + +BEING THE SYSTEM OF CLASSIFICATION ADOPTED IN THE PRESENT VOLUME. +(The Algae and Fungi rearranged in co-operation with Dr. E. Knudsen, the other Divisions as in the 3rd Danish Edition.) + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + C. Sub-Division: Fungi + Sub-Class: Fungi + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + Family: Pterosporaceae + +X + +
DIVISION I. THALLOPHYTAPAGE
A. Sub-Division. Myxomycetes, Slime-Fungi4
B. Sub-Division. Fungi5
Class 1. SENSIBILIA14
1. Dendrogyeta16
2. Schizogyma18
3. Dendrocyclus20
Family 1. Solanophyceae22
Family 2. Solanophyceae26
Class 5. CONIFERAE41
1. Coniferaceae45
Family 1. Prodoecocidium47
2. Coniferaceae53
3. Rhodophyceae69
Class 7. CHARACEA64
1. Porphyraea (Blue-Bay's Seaweed)68
Family 1. Porphyraea70
Family 2. Cystoseira73
Class 9. DEUTERELLAEAE76
+ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
X TABLE OF CONTENTS.
Class I. MUSCULES106
Sub-Class 1. Hemimni108
2. Hemiaridii109
Class II. MUSCULES (Fossi)114
Sub-Class 1. Anomocetes114
Series 1. Eozoni138A
Family I. Gymnastoles138
“ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ “ ““““““““““““““““““““““““““““““““““““““““““““““““““““““““““““““““““““““““““““““138A
” 2. Perisphorites138
” 3. Perisphorites138
” 4. Hysterotites139
” 5. Hysterotites139
” 6. Holothorax139
” Anaclochurn139
Sub-Class II. Prothoracites144
Series I. Prothoracites145
” Autobathycrites157
” Autobathycrites157
” Hysterothorax159
” Phalacronotus176
Fungi Imperfecti
DIVISION II. MUSCULAE (MOSSES)
Class I. HYPERICAE.
Family I. Marchantiae.
" " " " " " " " " " " " " " " " " " " " " " " " " " " " " "
" " Anochoeroces.
" " Jungenmannae.
Class II. Musci.
Family I. Sphenophytes.
" Schizomycetes.
" Schizomycetes.
" Schizomycetes.
" Schizomycetes.
" Schizomycetes.
" Schizomycetes.
+ +
DIVISION III. PTERIDOPHYTA
+ + + +
Class I. Filicaceae.
+ + +Sub-Class I. Filices. + + +Family I. Lepidostegiaceae. + + +Sub-Class II. Hydropteridaceae. + + +Class III. Psilotales. + + +Sub-Class I. Psilotaceae. + + +" Psilotaceae Equinulinae." + + +Class IV. Lycopodiales. + + +Sub-Class I. Lycopodiaceae. + + +" Lycopodiaceae." + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
TABLE OF CONTENTS.xii
TABLE OF CONTENTS.
TRIVIATION FROM THE CYANOPHAEAE TO THE PHAEOPHOREAE284
Lateral Generations of the Cyanophyceae284
Sexual Generation; Fertilization285
DIVISION IV. GYMNOSPERMÆ.285
Class I. CYCADACE (Cycadae)286
    2. Cycadace (Pine-Trees)285
Family I. Cycadace286
    2. Pinolidae287
Class II. Gymnospermae290
    1. Female Gymnospermae271
DIVISION V. ANGIOSPERMÆ.273
Class I. MONOCOTYLEDONIUM274
    Family I. Halimionaceae279
    1. Halimionum -  283
    2. Spadiceform -  297
    3. Eucalyptus -  308
    4. Eucalyptus -  309
    5. Seismium -  309
 310311312313314315316317318319320321322323324325326327328329330331332333334335336337338339340341342343344345346347348349350351352353354
+ + + +
Sub-Class I. Charophytaeum
Family I. Balleforiaceae
    2. Querciforium
    3. Juglandiforium
    4. Querciforium
    5. Polygoniforium
    6. Liriodendron
    7. Castelletum
    8. Polyparionum
    9. Rhododendron
    10. Rhododendron
    11. Clusiiform
&nb... + +xii + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +The corolla is strongly bilabiate (Figs. 573, 574, etc.), with 2 lobes in the upper lip and 3 lobes in the lower lip (an approach to regularity being seen in Mentha and Salvia). It resembles one lobe, as in Mentha (Fig. 575) and Scutellaria, so that the corolla approaches the 4-memoral corolla of Veronica and Plantago. The posterior stamen in the diagram (Fig. 574 *) is entirely suppressed; in some cases it is only partly suppressed; in others it is smaller (Fig. 573 D), and are entirely suppressed in some (see below); in others, e.g. Nepeta, they are the longer. 2 stamens are found in Salvia, Rosmarinus, Lycopus, etc. The two halves of the anther are united at their base by a short filament; they diverge at an angle with each other. The gynoecium has a style with a bifid extremity (Fig. 572 C) bearing this stigma; the true bilocular ovary is divided by a false partition-wall into 4 loculi, each with 1 erect ovule (Fig. 572 D). These a local project so strongly that the ovary becomes deeply 4-lobed with the style situated in + +NUCULIFERA. 537 + +the centre of the lobes and at their base, "gynobasic" (Figs. 575, 579). A ring-like, often crenate, necatory surrounds the base of the ovary (Fig. 575 $H$). The embryo in this order, as in the Verbenaceae, is directed downwards (Fig. 575 $J$) (it is directed upwards in the Verbenaceae, which have an entirely similar fruit). *Endogyna* absent. + +A botanical illustration showing the structure of a flower. +**Fig. 581. —Tropaeum vulgare.** + +The 143 genera are mainly distinguished according to the form of the calyx and corolla, the number, direction, and length of the stamens, the forms of the nuts, etc. + +1. *Augee*, *Buddleia*. Calyx 10-nerved; the upper lip is small; 4 stamens. The ovary is not so strongly lobed as in the following group, so that it is most nearly allied to the Verbenaceae. The nuts are reticulately wrinkled. *Augee* (Buddleia) has a very + +A botanical illustration showing the structure of a flower with a calyx and corolla. + +538 + +DIGOTYLEDONES. + +small upper lip. The upper lip of *Teucrium* (Germander) is deeply cleft, and the two lobes are bent on their respective sides towards the under lip, and so in consequence appears to be 2-lobed, and the upper lip to be wanting. +2. STECHERI, HETONY GROUP. The calyx is 5- or 10-nerved. +The upper lip of the corolla is most frequently strongly arched or incurved, and has 2 lateral lobes, the lower one being a stamen, the anterior pair the longer (Fig. 576). +a. A somewhat regular and 5-10- +dentate calyx with projecting stamens. +B. *Hemiphractus* (Hetony, +Woundwort), with the lobes of the under +lip are rounded off. +b. The anterior fila- +ments of the stamens are long, the pollina- +tion, bend outwards. +*Botanisia.* *Ballota* (Horehound); the calyx is funnel-shaped, and +has triangular, long, pointed, awn-like teeth.—*Galopis* (Hemp- +nettles). The calyx is 5- or 10-nerved, with +the lateral and the central lobes. +The anthers open by 2 unequal valves. +*Laxmann* (Dead-nettle); Fig. 576) has dentate, lateral lobes +on the under lip. *L. album* +(White dead-nettle); *L. alba* +brum, etc. *Galeodesdunia*—Loc- +nurra; *Phalotis.* +c. Tubular, regular, often +10-toothed calyx and con- +cealed stamens.—*Marrubium +vulgare* (Fig. 577). 10 only- +teeth, hooked at the apex; +much shorter than the length +of flowers in the axils of the +foliose-leaves; at some dis- +tance from one another.— +*Sideritis.* + +8 + +A longitudinal section of a leaf with stamens; B the same of a flower. +Fig. 576.—*Laxmann album*. A. Internal view of flower; B. Longitudinal section; C. Leaf with stamens; D. The same of a flower. + +8 + +A flower of *Botanisia.* +Fig. 577.—*Botanisia vulgaris.* + +**NUCULIFERA.** 539 + +flowering.—Scutellaria (Skull-cap); the two lips of the calyx are entire, the upper lip has a large spur, and drops off on the ripening of the fruit. The flowers are generally solitary and turned to one side.—*Prenula* (Meal-alk); the calyx is compressed, its two lips are strongly dentate, the upper lips closing slightly round the anther; the lower lip is long-pointed, and projects beneath the anther. + +3. *Nertera.* *Clammy Grass.*—13–15 nerves in the calyx; this deviates from the other groups in the posterior stamens being longer. The upper lip is slightly arched. *Nepeta* (Catmint), also *Glechoma* (Ground Ivy), with regular, and *Dracocephalum* with irregular calyx. + +A B +Fig. 573.—*Mentha aquatica*, var. crispa. + +4. *Satureiae.* *Mint Group.* The upper lip is flat, most frequently ovate, or almost spherical, and emarginate (Fig. 575). The calyx is most frequently 3–10-nerved. 4 stamens, the anterior ones of equal size; 2 lateral ones of unequal size (Mint, Fig. 575) has a regular 4-dentate calyx, a small, almost equal 4-partite corolla, and a erect stamens of nearly equal size. The verticillasters are many-flowered, and are often collected into cylindrical heads; the corollas are usually regular. 2 stamens, the posterior lateral ones wanting. +*Prenula*: 4-dentate calyx, 4-partite, regular corolla; 4 stamens of equal size.—Thymus (Thyme, Fig. 575) has a strongly bilabiate calyx; the corolla is regular; 2 stamens wanting (Fig. 576 A, B). The corolla is distinctly labiate. Under-shrub, with small entire-leaves; verticillasters few-flowered and separate.—*Origanum* (Marjoram); spike or capitose inflorescences with the flowers solitary- + +540 +DICOTYLEDONES. + +in the axils of the rather large and distinctly 4-rowed (often slightly coloured) floral-leaves. *Melissa.* Calamintha. *Cinquefo- +lium (Wild Basil).* *Satureia.* *Hympnae* (Hymnpa); small, entire, hairy, or glandular-stipulate, sessile or short-pedicelled, spike-like inflorescence. *Lavandula* (Lavender): shrubs with verticillasters collected in cylindrical, long-stalked inflorescences: the calyx is tubular, has 13–15 nerves, the posterior tooth is much larger than the others, and the style is not projected. *Cleome* differs, among other characters, in having united filaments of the stamens and style are bent down and concealed in the boat-shaped under lip. + +Image of a plant with a label "Fig. 479 - Satureia officinalis" + +**5. Monarda, Salvia Genus.** Only the 2 anterior stamens are developed.—*Salvia* (Fig. 559): calyx deeply bilabiate; the upper lip of the corolla is generally strongly compressed. Rudiments of the two lateral stamens are present. The connective in the two fertile stamens is very narrow and broad at the upper end, a narrow half-anther, but at the lower end a very broad portion, against which the insect is obliged to push its proboscis during its visits to the flowers, causing the pollen-bearing half-anther to be pressed down against its back. Floral-leaves: entire or crenate (Ramosa), linear-lanceolate with leathery linear leaves, with rolled back edge. A small tooth on the filament represents the barren half of the anther. *Monarda.* + +The pollination is generally effected by insects, especially bees; the underlip in the flowers of *Monarda* is often prolonged into a spur, pollina- +tion is promoted by dithegamy; honey is secreted by an hypanthial disc and collected in the corolla-tube. Some genera are homogamous (*Lavand., Galeo- +pia*, etc.); others are dithegamous (Gentianifera); a few are gynodioecious; + +Image of a plant with a label "Fig. 480 - Monarda officinalis" + +**CONTORTUS.** 541 + +*Q.* and *3-flowers in various relative sizes (Glechoma hederacea, *Tayusus*, *Sativia pratensis*, and others). The entrance of unincarnate flowers to the gustus is often rendered difficult by the presence of the stamens which sometimes intrude into the mouth. *Cotoneaster* is found in the *Leucanthemum* species. + +*Trollius*, distributed over the entire globe, but the greater number in Mediterranean countries (especially in the Eastern regions), where many are shrub-like. Poisonous and astringent are abundant. On account of their rich perfume, they are used in perfumery, and in *medicina* (the official parts are therefore nearly always "folia" and "herba"), in *Laudanum* the flowers, and the volatile oils extracted from them. Such plants are also used in medicine, especially in the treatment of nervous diseases, and from *M. arenaceus*—a little (*Spearmint*) *M. crispa* (Curly mint), *Thymus vulgaris* (Thyme) *Melissa officinalis* (Balm) *Eupatorium perfoliatum* (White mugwort), *O. vulgaris* (Wild Marjoram), *ceratonia, magnurnum, etc.* Sabina officinalis (Sweet basil) *Laurus nobilis* (Bay) *Caryophyllus aromaticus* (Rosemary) *Lavandula angustifolia* (Lavender) *Satureja montana* (Mountain savory) *S. hortensis* (Herb-sage) (*of Lavender, S. Eur.*). Also *Satureja montana* (*S. Eur.*), *Ocimum basilicum* (*E. Indica*, *Pogostemon patchouli* (*E. Indica*, etc.), *Anthemis tinctoria* (Yellow chamomile), *Chrysanthemum cinerariifolium* (White stem leaves), *Stachys lanata* (white, wooly), *Phlomis*, *Sativia species*, *Perilla*, etc. + +Order 6. **Salicaceae**: 130 species; most frequently heart-like shrubs or herbs, mainly from S. Africa. They differ from the other Noliceae especially in the bilocular, transversely-ovoid fruit with persistent calyx. The ovule has 2 or 4 by separation only 1 locule, each with 3 ovalets and the fruit is a achene dividing into two locules. The fruits are smooth. Tumble burr-owens—a few are ornamental plants (*Solanum*, Heterosperma). + +Order 7. **Glabridacaceae**: 18 species; especially in the Mediterranean. They form a group of plants with a very small flower, which is usually sessile in appearance, the flowers being crowded into a spherical head (hence their name) and supported by bracts, but without involucre; the ovary is trilocular and the fruit is a capsule with persistent calyx. + +The corolla is more or less labellate, the upper lip is often absent as in the ligularioids, circulo-ligulatae, simple or double; the petals are free or imbricated; the leaves are sessile, simple, entire, and generally form a rosette. Globularioides. + +Order 8. **Balanites**: 2 species; one of which is hairy; the leaves are linear; 1 erect seed in each locule; or posterior leaf is empty. *Balanites* 8 species. S. Africa. + +Family 20. **Contortae**. + +*Hypogynum*, regular; 3♀ gamopetalous flowers (Figs. 581, 582), which are generally 5 or -merous, with 5 or 8 stamens (with the exception of *Oleaceae* and *Jasminaceae* which have only 2 stamens, alternating with the carpels). The gynoecium is formed of + +These which are official are indicated by c. + +| Species | Description | +|---|---| +| Glechoma hederacea | A perennial herb with creeping stems and opposite leaves; small white flowers in axillary clusters; leaves oval-oblong to elliptic-lanceolate; flowers small white; sepals oblong-lanceolate; petals oblong-lanceolate; stamens numerous; style short; fruit a small globular achene | +| Tayusus | A perennial herb with creeping stems and opposite leaves; small white flowers in axillary clusters; leaves oval-oblong to elliptic-lanceolate; flowers small white; sepals oblong-lanceolate; petals oblong-lanceolate; stamens numerous; style short; fruit a small globular achene | +| Satvia pratensis | A perennial herb with creeping stems and opposite leaves; small white flowers in axillary clusters; leaves oval-oblong to elliptic-lanceolate; flowers small white; sepals oblong-lanceolate; petals oblong-lanceolate; stamens numerous; style short; fruit a small globular achene | +| Cotoneaster | A genus of shrubs or trees with opposite leaves and small white flowers in axillary clusters; leaves oval-oblong to elliptic-lanceolate; flowers small white; sepals oblong-lanceolate; petals oblong-lanceolate; stamens numerous; style short; fruit a small globular achene | +| Trollius | A genus of plants with opposite leaves and small white flowers in axillary clusters; leaves oval-oblong to elliptic-lanceolate; flowers small white; sepals oblong-lanceolate; petals oblong-lanceolate; stamens numerous; style short; fruit a small globular achene | +| Salvia pratensis | A perennial herb with creeping stems and opposite leaves; small white flowers in axillary clusters; leaves oval-oblong to elliptic-lanceolate; flowers small white; sepals oblong-lanceolate; petals oblong-lanceolate; stamens numerous; style short; fruit a small globular achene | +| Thymus vulgaris | A perennial herb with creeping stems and opposite leaves; small white flowers in axillary clusters; leaves oval-oblong to elliptic-lanceolate; flowers small white; sepals oblong-lanceolate; petals oblong-lanceolate; stamens numerous; style short; fruit a small globular achene | +| Melissa officinalis | A perennial herb with creeping stems and opposite leaves; small white flowers in axillary clusters; leaves oval-oblong to elliptic-lanceolate; flowers small white; sepals oblong-lanceolate; petals oblong-lanceolate; stamens numerous; style short; fruit a small globular achene | +| Eupatorium perfoliatum | A perennial herb with creeping stems and opposite leaves; small white flowers in axillary clusters; leaves oval-oblong to elliptic-lanceolate; flowers small white; sepals oblong-lanceolate; petals oblong-lanceolate; stamens numerous; style short; fruit a small globular achene | +| Ocimum basilicum | A perennial herb with creeping stems and opposite leaves; small white flowers in axillary clusters; leaves oval-oblong to elliptic-lanceolate; flowers small white; sepals oblong-lanceolate; petals oblong-lanceolate; stamens numerous; style short; fruit a small globular achene | +| Laurus nobilis | A deciduous tree with alternate leaves and small white flowers in axillary clusters on long peduncles); leaves ovate-oblong to elliptic-lanceolate or oblanceolate, acuminate at apex, obtuse at base, glabrous beneath except for scattered glandular hairs on midrib below middle of leaf blade); flowers small white, fragrant, solitary on long peduncles); sepals oblong-lanceolate or linear-oblong, acute at apex, obtuse at base); petals broadly ovate to orbicular-ovate, obtuse at apex); stamens numerous); style short); fruit a globose achene | +| Caryophyllus aromaticus | A perennial herb with creeping stems and opposite leaves); leaves ovate-oblong to elliptic-lanceolate or oblanceolate, acuminate at apex, obtuse at base); flowers small white, fragrant, solitary on long peduncles); sepals oblong-lanceolate or linear-oblong, acute at apex, obtuse at base); petals broadly ovate to orbicular-ovate, obtuse at apex); stamens numerous); style short); fruit a globose achene | +| Lavandula angustifolia | A perennial herb with creeping stems and opposite leaves); leaves ovate-oblong to elliptic-lanceolate or oblanceolate, acuminate at apex, obtuse at base); flowers small white, fragrant, solitary on long peduncles); sepals oblong-lanceolate or linear-oblong, acute at apex, obtuse at base); petals broadly ovate to orbicular-ovate, obtuse at apex); stamens numerous); style short); fruit a globose achene | +| Satureja montana | A perennial herb with creeping stems and opposite leaves); leaves ovate-oblong to elliptic-lanceolate or oblanceolate, acuminate at apex, obtuse at base); flowers small white, fragrant, solitary on long peduncles); sepals oblong-lanceolate or linear-oblong, acute at apex, obtuse at base); petals broadly ovate to orbicular-ovate, obtuse at apex); stamens numerous); style short); fruit a globose achene | +| Chrysanthemum cinerariifolium | A perennial herb with creeping stems and opposite leaves); leaves ovate-oblong to elliptic-lanceolate or oblanceolate, acuminate at apex, obtuse at base); flowers yellowish-white or pale yellowish-green), solitary on long peduncles); sepals oblong-lanceolate or linear-oblong, acute at apex, obtuse at base); petals broadly ovate to orbicular-ovate, obtuse at apex); stamens numerous); style short); fruit a globose achene | +| Balanites aegyptiaca | A deciduous tree with alternate leaves and small white flowers in axillary clusters on long peduncles); leaves ovate-oblong to elliptic-lanceolate or oblanceolate, acuminate at apex, obtuse at base); flowers small white, fragrant, solitary on long peduncles); sepals oblong-lanceolate or linear-oblong, acute at apex, obtuse at base); petals broadly ovate to orbicular-ovate, obtuse at apex); stamens numerous); style short); fruit a globose achene | + +Note: The descriptions provided for each plant species include its common name(s), scientific name(s), habitat(s), growth habit(s), flower color(s), flower arrangement(s), leaf shape(s), leaf arrangement(s), leaf margin(s), leaf venation pattern(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s), flower arrangement(s), flower color(s), flower arrangement(s), flower structure(s). + +542 +DIOTYLEDONES. + +2 (nearly always median) carpels. The corolla very frequently has twisted antecollis (the upper edges of the petals being free; Fig. 581 A), and hence the individual lobes of the corolla are oblique, with the lower edges of the lobes being free (Fig. 581 B). A nectary, in the form of a honey-secreting ring or glands, is often found round the base of the corvey.--The leaves, with a few exceptions, are opposite and without stipules. Endosperm large (Fig. 581 C), except in some species of *Astragalus*. + +The *Astragalus* and the *Aselephas* alone, account for the two genera, without which there would be no more primitive form, but the *Aselephas* alone have on their other hand an outshoot on account of their peculiar pollen-masses. The *Lupinus* shows a transition to the *Robinia*. + +The order is: + +A. *Stemum* 5. 1, Gentianaceae; 2, Aporocerae; 3, Aselephas; 4, Loga- +naceae + +B. *Stemum* 5. 2, Oleaceae; 6, Jasminaceae; 7, Salvadoraee. + +Order 1. Gentianaceae (Gentians). Glabrous herbs, with- +out latex; the opposite, undivided and entire leaves are often slightly united at the base; many have rosette-like radical leaves. +*Sugillus* absent. The flowers are generally borne in regular, dichotomous-branched corymbs (Fig. 581 D); the calyx is becoming transformed into unpaired scapoid cyms; the parts of the flower are 4-merous as far as the gynoeceum, which is 2-merous; the perianth is usually polysepalous; the corolla has distinctly twisted antecollis (the upper edges being free) (Fig. 581 A), except *Mimulus*, which has its lobes entirely united, and most frequently form a 1-lobed ovary with 2 pa- +rietal placentae bearing many abortive (often sterile) stamens (Fig. 581 E). +Fy. *Crepida*, 2-valved, with septi- +cidal clefts, the incurred cymes +bearing the seeds (Fig. 581 D, F). + +Fig. 580.--Erythraea. Inflorescence. +I, II, III, etc., the succulent shoc- +gonermae. + +*Gentiana* has most frequently a tubular, campanulate or funnel-shaped corolla, sometimes with teeth between the corolla-lobes and fringed in the throat of the corolla; *G. Intusa* has a rotute, yellow corolla.--Serrata: rostrate corolla; each lobe has at its base 1-2 membrae, with fringed edges. + +542 + +CONTORTE. +543 + +Erythraea (Centaurcy, Fig. 581); corolla most frequently salver-shaped. The authors ultimately become spirally twisted (B). The style protrudes from the corolla, but is not prolonged into a spur, i.e. the median sepal is anterior; the corolla is rose-coloured (in the native species). The capsule is semi-bilocular (Fig. 581 F, G). + +Chondria has a low creeping stem, fine as a thread, and small, yellow flowers, 4-merous (without twisted sepal), —Chion (Yellow-wort) 6-merous. + +![Image of Chondria plant] +Fig. 581.—Chondria punctata. Inflorescence, flower and fruit : left, leaf-tuft-leaves of the last and Bud-stater ; right, a view of the capsule. + +2. MENTHARIA. Menthaeae (Mint-family) deviates in several respects from the type of the order. The leaves are scattered and in *M. trifoliate*, trifoliate; the corolla has eulate estivation; the teeth are also very hard (thin in the true Gentianae). They are squarrose, with a long terminal spur; the flowers are in racemes, with terminal flower, heterostylous. The corolla is funnel-shaped with a very hairy throat. —Lemnaceae with floating leaves, like the Water-lilies. + +575 species, distributed over the entire globe, but most numerous in *Alpine countries*. Neither poisonous nor nutritive plants are found, but several are used in medicine on account of the bitter properties so prevalent amongst them. + +Oxymyrtus: the genus of *Gentiana* (Gentianae) is included in this order (Fig. 581 G, H). The perianthments and sepals (Europe) and the leaves of *Menthaeae tri- meres* are medicinal. Some are grown as ornamental plants on account of their perfume. + +Order 2. Apocynaceae (Periwinkles). Trees and shrubs (also lianes), less frequently herbs, generally with latex. The leaves are opposite, simple, entire, without stipules; the flowers are W. B. +N N + +544 +TETRACELEONES. + +regular; corolla-lobes oblique, estivation twisted. The stamens are individually free, and the pollen-grains are free or at most united in four (see Asclepiadaceae). The two carpels have 2–3 ovules, in one of which only one is fertilized, a capitulate stigma, which towards the base is widened out into a disc-like structure (the disc) abstricted in the centre; but the carpels in most of the genera (as those mentioned below) are entirely separate, and the fruit consists of two follicles, of which often have a tuft of woolly hairs growing from the middle of each, and sometimes two drosses. In some other genera there is a 1-locular (provided with 2 parietal placentae) or a 2-locular ovary becoming a 2-valved capsule (see Asclepiadaceae). *Pison* (Viticaria) has a single ovule, which is twisted to the left (as the left edge of the petals is free); neotaries, alternating with the carpels; the summit of the style is hairy; *Follicles*; seedless without hairs. Mostly creeping, perennial, evergreen, plants. The leaves are simple, alternate, entire, or lobed; they are terminal, but by the development of the bud in the axil of one of the two uppermost leaves, they are displaced over the other leaf of the pair to become sessile (i.e., forming a "false" leaf on top of the drape"); *Aegopodium*. *Nerium* (Oleander). The leaves are in whorls of 3. Corolla funnel-shaped in estivation twisted to the right; and with a corona resembling that of *Lycium*. The anthers are prolonged at the base and each also bears at the apex a long, linear, hairy appendage; these finally become spirally twisted. *Follicles*; each hairy *Apocynum*, *Cynanchum*, etc.; *Apocynum* is epigynous. + +1871. *Asclepias* is principally in North America. The species of *Ficus* are natives of this country; the following are cultivated as ornamental plants—*Ficus sinensis*, M. fajer, F. (Lacherae) rasa, *Asclepias trifolia*, *Saururus canadensis*, *Asclepias tuberosa*, *Asclepias tuberosa var. floridana* (Taynsha floridana), *Coriaria*. Cocoon-stitch is obtained from others (*Elaeagnus*, *Hamamelis*, *Fakah*, etc.). Tough bark is frequently developed. The bark of *Corylus avellana* is used in medicine (also for African arrow-poison), the latter is official. + +Order 3. Asclepiadaceae. A recognised and easily recognised order, closely allied to the Apocynaceae, having, like it, frequently a poisonous latex, opposite, simple, entire leaves and fundamentally the same flowers. The corolla is usually 5-lobed; but in some the stamens are united in most of the corolla as valvate. The carpels here also have free ovaries, but are united for some distance above into a large, shield-like, 5-angular head, having on its under-side + +CONTOYR. +545 + +the true stigmas, and the fruit always consists of 2 follicles; seeds most frequently numerous and hairy at the micropyle ("vegetable silk"); endocarpus scantus.--The order is distinguished from the Aspogynaceae and from all other plants also, except the Orchids, by having two or more (usually three) sessile, free, and sterile anthers (true 2-localan anthers) united into one unitary, club-shaped pollenarium ("pollinum"), for the purpose of pollination by insects. These heavy masses, in order to secure pollination (as in the case of the Orchids), are often provided with a sticky disc (corpusculum); there are 3 corpuscula, one at each of the corners of the 5-angular stylar base (which is within the anthora), and to each of these are attached 2 pollinia, one from each of the authors situated on the same side (carnes), each author gives its right pollinium to one corpusculum and its left to another). The stamens are frequently united at the base (staminodia), on the back a varicously formed, petaloid appendage, termed a "cucullus" (fig. 86). + +The perianth is in a peculiar relative position (and therefore a good, distinctive characteristic is often found in the infructescence), it is symmetrical, but bent downwards towards the two leaves of a whorl, nearer to one than to the other. + +The leaves are usually large, in the floral region, as node and axile angles, and not at right angles; they are either entire or serrated; the pistils are placed in two rows only which are nearly 90° from each other. The stamens contiguous to one another are anatropous; those contiguous to one another are antitropous; they are in one or two series (one series in each case), and the entire floral portion of the shoot is + +![Image](image-url) + +Fig. 86.--Aspidistra stricta. A &h open flower. B &h closed flower. At first opened corolla droop down; the stamens are bent together and their filaments are united at their base (after removal of the stamens parts (corollae)). C &h closed flower. D &h a view of a corolla. E &h the inner expansion of the fertile anther. F &h the outer expansion of the sterile anther. G &h a view of a fertile anther showing that part of the pollenium which is unable to be deposed, because it is united with the fertile anther part corpusculum; this part corpusculum hides a short anther in its internal cavity. H &h a view of a sterile anther which is split at its base and joined on either side by a short anther part corpusculum (same as fig. E). When the bud of the flowers is complete (in the state I.) both parts of the corolla are spread out in such a way that both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes are opposite to each other; when fully expanded, both corolla lobes + +546 +DICOTYLEDONES. +a unipared sessorial cymose sympodium; in addition, complications also arise through individual parts becoming united—Herbs and shrubs, some twining or climbing. + +In *Aesculus* the corolla is bent back and there is a cup-like cucullus, from the base of which protrudes a horn-shaped body, bent inwards—*Vincetoxicum* has a rotate corolla and a ring-like, 5-lobeled cucullus, without internal prominences.—*Staphisagria* (especially from S. Europe) has a cup-like cucullus with 5 large, brownish flowers, often with caruncle-like smell. *Ferghana* has more pearly podaria (S. Eur., etc.). *Ipecacuanha* (Wax-flower; Trope, Asia) is a climber, with a cup-like cucullus. The genus *Cynanchum* comprises 304 genera with 1700 species, distributed over all continents; few outside these limits: no native species. Several are used in medicine on account of their bitter taste. *Cynanchum* is a genus of medicinal plants. *Cynanchum* is obtained from the latex of some (e.g., from Cynanchum). The medicinals, which are most frequently utilized, silk-leafs, and the like, are used for their great value. Ornamental plants in our gardens: *Aesculus*, species, etc. + +Order 1. *Cucurbitales*. The leaves are opposite or alternate. The inflorescences are racemes or panicles. The calyx and corolla are 4-morose, more or less united, free in some species; the corolla has mostly numerous valvate estivation. All four forms of fruit occur (see the following figures): *Cucurbita* (Fig. 851), *Cucurbita maxima* (Fig. 852 C), *Espinosa* (Lilac) and *Forfexia* (anthers somewhat extorse) have capsules with loculicidal dehiscent valves; the flowers are saled and sometimes unilocular (polygamous), the Mannan Ash (*F. ovata*) has however a double perianth with 4 free petals (Fig. 853 e); in the native species, *F. esculenta*, + +CONTOUR. 547 + +the flowers open before the foliage appears.--Ligustrum (Privet) has berries.--Olea (O. europaea; Oliver) has drupes; the pulp and seeds of the ellipsoidal fruits are rich in oil. The lanceolate leaves are grey on the under surface, being covered with stellate hairs. In the wild state, this tree is rare (modestum; var. canum).--Philodendron; Chionanthus.--Few species of *Ligustrum* have 4 stars. + +A diagram showing four different views of a plant, labeled A, B, C, and D. +Fig. 303.--*Pentas* (Pentas), A flower, or calyx, or corolla; B gymnosperm and calyx; C gymnosperm and corolla. + +180 species; chiefly in the northern temperate zone. The Oleaceae (olive) genus has been an important cultivated plant from ancient times (Oliva olive, Provence olive, "Sessé" oil). The best oil is extracted from the fruit-pulp. +The tree is native to the Mediterranean region, but is widely naturalized. The Ash (Fr. *cercidier*, *Quercus*); the Mannar Ash (Fr. *crassifolia*, cultivated in the Mediterranean countries for the sake of its sandarachy juice, which flows out and cures wounds); the *Celtis* (Fr. *cèdre*); the *Corylus* (Fr. *châtaîn*); the *Quercus* species of *Ligustrum* and *Syringa* (introduced in the 16th century, from S.E. Europe and Asia); Forsythia (China, Japan); the large, yellow flowers are borne on spreading branches with long petioles (long petiole leaf), Chionanthus. + +Order 6. Jussimaceae. The anastomosis of the corolla is suborbicular ; the calyx is usually 5-lobed without epipetals ; radicle directed downwards. +The number of lobes in the calyx and corolla is not 4, but e.g., 5, 8, 10, and variations are sometimes observed in the same plant. The fruit is a berry or capsule, and is often two- or three-seeded. This manner of fruiting is seen most frequently in Impatiens.--120 genera; especially in trop. Asia (6. India). +Some Jussimaceae are used medicinally; they contain a bitter juice; their dicotyledons account for their elegant foliage, and beautiful scented flowers, the essential oil of which is also used in perfumery; the best known are: J. sardanica; J. sanguinea; J. sanguinaria; J. cordata; J. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. cordifolia; J. cordifolia var. +Order 7 (?). Salvadoraeeae.--8 species; Asia, Africa--Salvadora. + +547 + +248 + +**DIOCTYLEDONAE.** + +**b. Tetracyclicum with epigynous flowers.** + +Family 33. *Rubiaceae*. + +The leaves are always opposite or verticillate. The flower is epigy- +nous, $q^{\prime}$, $3$- (or $4$-) merous, with the usual sympetalous diagram; + + +Flowering branch. + + +Fig. 564.—*Cordia colossus*. Flowering branch. + +2-5 carpels. The inflorescences are frequently dichasial. The sepals are small, reduced to teeth, and become almost entirely exserted in the higher forms.—The flower is regular in *Rubiaceae* + +RUBIALES. 549 + +and some Caprifoliaceae, but in other genera of this latter order (especially of Lonicerae) it is unsymmetrical. In several genera of the order, the ovary is unilocular, with one or two many-ovuled, but in the last the number of local and ovules becomes reduced. This is to some extent connected with the nature of the fruit which is many-seeded in most instances, namely a capsule or berry, but in others mullike. Indeterminate is present. + +The family on one side is allied to the Convolvulaceae (not only through the Lonicerae), and on the other side to the Solanaceae, which are treated as an epigynous continuation of this family; on the other side it is allied to the Valerianaceae and Dipsacaceae. Many points of agreement with the Coriaceae and Scrophulariaceae are found in Rubiaceae, but these are distinguished from these by having any other feature than the gamopetalous corolla. + +Order 1. Rubiaceae. Leaves opposite (or verticillate), undivided and entire, with interpeticular stipules (Fig. 386). Flowers + +A B C D +Fig. 386.—Cotonea calycina. A. a flower; B. at the removal of the corolla; C longitudinal section of corolla; D. fruit. E. + +epigynous and hermaphrodite; regular, or 4- or 5-membranous with the nema arrangement (Fig. 387); stamens usually 4 or 5, sometimes gamopetalous, in initiation often velutinous; ovaries frequently 2-locular. + +There are no external characters which at once distinguish this exceedingly large order, as in many other natural orders (Compositae, Umbelliferae, etc.), but they are so numerous that they form a very useful point of recognition. It is divided into many sub-orders and groups, especially characterised by the nature of the corvey (or several ovules in each locule), and of the stamens (whether monadelphous or polyadelphous), and by the number of genera; its variation in size is twined; in Caprifoliaceae, etc., the filaments are unequal in size. The corvey is semi-gamopetalous in Hesperidaceae, etc. In Mirandia all the flaky fruitle conduce into one multiple fruit. + +549 + +550 + +DIOTYLEDONIUM + +1. **Cynocereus**. The fruit is a 2-valved capsule, with many winged seeds (Fig. 583). Cucukosa (Quinina, Fig. 584). Trees and shrubs with the foliage and inflorescence somewhat resembling *Syringa* ; the corolla also being of a lilac colour, more or less salver- or funnel-shaped, and frequently edged with a fringe of hairs (Fig. 585), is found in the Andes of Mexico. *Mephisto*, in the Andes from Bolivia to Venezuela, varying in altitude from 1-3000 metres. There are now large plantations in Java and E. India. (The name is derived from the Greek "mephistos," a demon, from the Spanish Diables Cachou, who in 1669 first introduced the bark into Europe.) The following are closely allied : *Cinclocera*, Itamica, Lantanaecium, Manicaria, *Lantana*. + +2. **Grewia**. Trees and shrubs, frequently having a many-lobular berry. *Blandia*, Gardenia, Graptole, Hemicla, etc. + +3. **Coffee**. Only 1 seed in each of the two loculi of the ovary; the fruit is a drupe with 2 stones. Coffea has an ellipsoid fruit (Fig. 586) with a thick, smooth, green skin; the core of a cherry; the two thin- shelled, parchment-like stones are enclosed by a hard, fleshy pulp; the two seeds are flat, the side turned to one another, which has also a deep, longitudinal groove running to the sides. The endo- sperm is hard, horny and starchless; the mesocarp is thin on the lower end near the circumference. The Coffee-plant (*C. arabica*) is a small tree, or more frequently, and especially in plantations, a shrub with large dark-green leaves and scented, white flowers. Its home is in Tropical Africa; its fruits are used for coffee (see *Cicer*). *C. olivieria*, W. Africn.--*Cephelis* (*C. occidentalis*, Fig. 585); the roots are official)--*Psychotria*, Chicoena, Incau, Hydrangeum, *Myr- secus*, etc. + +4. **Sterculia**. Chiefly small shrubs and herbs, many of which are weeds in tropical countries. The stipulate sheath bears numerous bristles at the edge. + +5. **Stellaria**. Herbaceous plants with pinnate leaves (Figs.). + +Fig. 583.—Cynocereus (quincinum). Portion of a branch & stipules. + +KUHILES. +551 + +587, 588-590) : the stipules are large, leaf-like, and resemble the lamina of the leaves, so that the leaves appear to be placed several in a whorl, while in reality there are only two opposite leaves, the stipules of which project freely, and are not erect (Fig. 587). + +In some cases there are apparently 6 leaves in the whorl, and then 3 of them are very small, and are called by some "false leaves." When + +A plant with small, leaf-like stipules at the base of each leaf. +Fig. 587.—Salvia thunbergii. + +there are apparently 6 leaves, then the two of these which are opposite each other are leaves, and the other four are stipules. If there are several members in the whorl, then a division of the stipules has taken place. The proof of this theory is founded upon the fact that not more than 2 of the leaves in a whorl ever grow together (the two opposite ones being always distinct), and also that the whorls do not alternate with each other, which, according to the rules of the position of the leaves, they should do if all the members of a whorl had + +502 + +DICOTYLEDONES. + +equal value. If these are, for instance, 4 members in two successive whorls, they stand right about each other, and are thus intercalated. The development and assiminal relations (the bearinging of the venation bundles) also point to the same conclusion—All the other groups of the order have only 2 small sub-like interpetiolar stipules, or they form at the base of the leaf-stalks a pair of small, often petiole-like, stipular leaves (Fig. 586). Another characteristic feature in this group is that the calyx is rudimentary; the corolla enfolds (Fig. 585), and that each of the two leaves of the corolla has only 1 ovary. The fruit is a silique, with a single seed; but in some species, such as *Corydalis*, it is a fruit, as well as many other characters, as, for example, the epigynous flower, the rudimentary calyx, the two free or almost free styles, presenting interesting analogies to those of *Corydalis*. This group has its home chiefly in the temperate regions of the northern hemispheres, especially about the Mediterranean; it is the only group which occurs in this country, represented by 4 genera. + +
TABLE OF CONVENT.Page
Sub-Class 3. Sproutacidae304
J. Pentacellicus306
Family 36. Bicorniae306
"287
"511
"Tetracongulina511
Family 37. Tetracongulinae511
S. Personatam517
"Nunifera541
"Bulbosa541
"Bulbosa246
"Campasumilum550
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8 + +2 CLASSIFICATION OF THE VEGETABLE KINGDOM. + +bundles. The lowest Mosses have, however, a thallus. Fertilisation is accomplished by means of self-mitosis, spirally coiled spermatoidons, through the agency of water. From the fertilised oosphere a "fruit-body" (capsule) with unicellular organs of reproduction arises ; this pericarp gives rise to the vegetative system, which bears the organs of sexual reproduction ; and this system is divided into two stages—the prothallus, and the leaf-bearing plant produced on it. + +Alternation of generations : + +I. The prothallus and the entire nutritive system which bears the organs of sexual reproduction. +II. The capsule-like sporangium, with spores. +3 Classes : 1. Bryophytes. +2. Mucil. Lentin. Mosses. + +Division III.—Pteridophyta or Vascular Cryptogams, +Fern-like Plants having leaf-bearing shoots, true roots, and vascular bundles with tracheides and sieve-tubes. Fertilisation as in the Mosses. From the fertilised oosphere the leaf-bearing shoot arises, which bears on its leaves the reproductive organs, the spores, and the capsule-like sporangium. Upon the germination of the spore a small prothallus is formed, which bears the sexual reproductive organs. + +Attention of generations : + +1. Prothallus with organs of sexual reproduction. +2. Leaf-bearing shoot with capsule-like sporangia. + +3 Classes : 1. Filicinae, True Ferns. +2. Equisetinae, Horsetails. +3. Lygodinae, Club-mosses. + +Division IV.—Gymnospermae. The vegetative organs are in the main similar to those in the 3rd Division; special shoots are modified into flower-stalks bearing cones. From the fertilised oosphere, which is fertilised by means of the pollen-tube, the leaf-bearing plant is derived ; this passes the first period of its life as an embryo in the seed, and continues its development when the gametophyte dies off. The pollen-grains are similar to those corresponding to the spores of the two preceding Divisions, are called respectively the pollen-grain and embryo-axe. The pollen-grains are multifoliar; i.e. they contain an indistinct prothallium. In the embryo-axe a prothallium, rich in reserve material (endosperm), + +CLASSIFICATION OF THE VEGETABLE KINGDOM. +3 + +with female organs of reproduction, is developed before fertilisation. The pollination is carried by means of the wind to the ovules; these are enclosed in the ovaries, and are situated on the open fruit-leaf (carpet), which has no stigma. + +Alternation of generations: +I. Plant-forms with two stamens in ovule. +II. Leaf-bearing plants, with flowers which produce the pollen-sac and ovule. + +3 Classes: 1. Cycadeae. +2. Coniferae. +3. Gnetaeae. + +Division V. Angiospermae. The members of this group are very similar to those of Division IV. The ovules are, however, enclosed in closed fruit-leaves (ovary), which have a special portion (stigma) adapted for the reception and germination of the pollen-grain. The pollen-grains are bicellular, but with only a membrane separating the two cells; one cell is directed towards the stigma by animals (chiefly insects), by the wind, or by some other means. Endosperm is not formed till after fertilisation. Alternation of generations in the main is that in the Gymnosperms, but less distinct ; while the sexual generation, the protogynous, with the organs of fertilisation in the same leaf, is more common. + +2 Classes: 1. Monocotyledonae. Embryo with one seed-leaf. +2. Dicotyledonae. Embryo with two seed-leaves. + +For a long time the vegetable kingdom has been divided into Caryophyllae (so called because they contain seeds in a cup-like receptacle), and Phanerogamae or Flowering-plants which have evident sexual organs. + +The first three divisions belong to the Caryophyllae, and the third and fourth divisions to the Phanerogamae. This arrangement has no systematic value, but is very convenient in many ways. + +The first division is known as Spore-plants, since they multiply by unicellular organs (spore), and the Phanerogamae in contradistinction are called Seed-plants (Spermatophyta), since they multiply by seeds, multicellular bodies produced by the fusion of two gametangia (spore). The first division includes in its infancy, Mosses, Ferns, and Gymnosperms are together known as Archeophyta, while their powers in common a female organ of distinct structure, the Archegonium. + +3 See Angiospermae. + +4 + +THALLOPHYTA. + +DIVISION I + +THALLOPHYTA. + +The thallus in the simplest forms is unicellular; in the majority, however, it is built up of many cells, which in a few instances are exactly similar; but generally there is a division of labour, so that certain cells undertake certain functions and are constructed accordingly, e.g., the cells of the thallus may be divided into conducting structures, vessels or similar high anatomical structures, or seldom formed, and the markings on the cell-wall are with few exceptions very simple. The Myxomycetes occupy quite an isolated position, and masses of non-division are naked masses of protoplasm (plasmodium). + +As regards the external form, the thallus may be entirely without special prominences (such as branches, members), but when such are present they are usually of a definite origin and growth, that is, disregarding the hair-structures which may be developed. A shoot of a Seaweed or of a Lichen, etc., is essentially any other part of the plant; only among the highest plants (Chlorophyta) certain Sporangia, Spermogonia, and other Red Seaweeds do we find some differences between the various external organs of the plant body as between stem and leaf, so that they must be distinguished by these names. + +*Roots* of the same structure and development as in the Secl- +plants are not found, but *organs of attachment* (rhizoids and lamina) serve partly the bodily functions of the root. + +SYSTEMA TYPIUM OF THE THALLOPHYTA includes the Thallophytes belonging to the sub-divisions: Slime-Fungi, Algae and Fungi. +Formerly the Thallophytes were divided into Algae, Fungi, and Lichens. But this last group must be placed among the Fungi, +since they are composed of Fungi, which live symbiotically with Algae. +The Slime-Fungi must also be placed among the Fungi as a distinct sub-division. The *Alga* is a colouring substance, +which is generally green, brown, or red, and by means of which they are able to obtain their organic nutrition from carboxic acid and water. +The Bacillariophyta form a distinct group within the Algae in this respect; like the Fungi and Slime-Fungi they have as a rule no such colouring material, but must have organic car- +bonaceous food; those plants form no starch, and need no light + +MYXOMYCETES. 5 + +for their vegetation (most Fungi require light for fructification). The Myxomycetes, Bacteria, and Fungi derive their nourishment either as saprophytes from dead animal or vegetable matter, or as parasites from living animals or plants (hosts), in which they very often cause disease. + +A remark, however, must be made with regard to this division. Among the higher plants no means exists to halt the vegetative process until death has taken place. In the case of the Algae (Chlorophyta), a parasitic, is placed among the Conjugatinae, Noctuia and Conularia, saprophytes, belong to the Conjugatinae, and are found in the soil. In the same manner there are some ciliates parasitic or saprophytic forms among the Algae, and these must be laid upon the fact that not only the Blue-green Algae, but also the Green Algae, are parasitic on other organisms. The Blue-green Algae group, Siphonoclora. The reason for this is that cytometric classifications must be based upon the relationship of form, development, and reproduction, and from this point of view it appears that the Blue-green Algae are a subdivision of the entire group of Fungi. All the Thallophytes, which are designated Fungi (when the entire group of Fungi is considered), are included in the blue-green form (Fizymycetes) and are therefore classified as Algae. But probably through them has taken its origin from the Algae; the blue-green algae being a subdivision of the Fungi. The distinction of colour referred to is therefore not the only one which separates the Algae from the Fungi, but it is almost the only characteristic mark by which we can distinguish between these two groups of organisms. + +The first forms of life on earth were probably "Protista," which had assimilating matter in or on other words, they were Algae because they could absorb food from their surroundings. These were followed by those which belong to the simplest forms of all plants. Fungi and Slime-Fungi must have appeared later, because they are dependent on other plants which assimilate food. + +Sub-Division I—MYXOMYCETES, SLIME FUNGI. + +The Slime-Fungi occupy quite an isolated position in the Vegetable Kingdom, and are related to those which are most nearly related to the group of Rhinopods in the Animal Kingdom. They live in and on organic remains, especially rotten wood or leaves, etc., on the surface of which their sporangia may be found. + +They multiply by means of spores, which in the true Slime-Fungi grow into mycelium. According to recent investigations of Wasmann's mode micro-organisms (Nitzschia) have been found in these fungi. Such hypothesis that the first organisms must necessarily have contained chlorophyll is therefore untenable. + +I Myxogastera, Engler's Syllabus, p. 1. + +6 + +MYXOMYCETES. + +are produced in sporangia, but in some others free. The spores are round cells (Fig. 1 a) which in all the true Slime-Fungi are surrounded by a cell-wall. The wall bursts on germination, and the contents float out in the water which is necessary for germination. They move about with swimming and hopping movements, and are provided with a cell-nucleus and a pulsating vacuole. Later on + +A series of images showing the development of "Fuligo" from spore to Myxamoeba, each one magnified 300 times; m is a Myxamoeba of Egypto epedemica; Phymo Myxamoeba of Pigeon's alveolus; and Myxamoeba of the sea. + +FIG. 1.--A Development of "Fuligo" from spore to Myxamoeba ; each one magnified 300 times; m is a Myxamoeba of Egypto epedemica; Phymo Myxamoeba of Pigeon's alveolus; and Myxamoeba of the sea. + +they become a little less active, and creep about more slowly, while they continue to alter their form, shooting out arms in various places and drawing them in again ($g$, $h$, $i$, $k$, $l$, $m$); in this stage they are called Myxamoebae. + +The Myxamoeba is a plant whilst taking up nourishment from the material in which it lives, and multiplies by division. At a later stage a larger or smaller number of Myxamoebae may be seen to + +6 +Acreaen and Pitcomorphorales, Ibd. + +MYXOMYCETES. +7 + +oculose and form large masses of pteleophan, plasmodia, which in the "Flowers of Tain" may attain the size of the palm of a hand, or even larger, but none of them are smaller. The plas- +modia are independent, cream-like masses of protoplasm, often containing grains of carbonite of lime and colouring matter (the infarctus), and are very active. + +They creep about in the decaying matter in which they live, by means of amoeboid movements, internal streamings of the pro- + +A. Four sporangia of Sirovitsa jaceae, fixed on a branch of the plant. + + +Fig. 2.—The plasmodium (a) of Sirovitsa jaceae, com- +mencing to form into sporangia (b). Down on July 8th. The sporangia (c) are seen at different stages of their +life next morning ; e shows the development of their +toplam continually taking place; finally they creep out to the surface, and very +often attach themselves to other objects, +such as Mosses, and form sporangia (Fig. +3). These are usually cylindrical (Fig. 3), spherical +or pear-shaped (Fig. 4); they rarely attain +a larger size than that of a pin's head, and +are red, brown, white or yellowish with a very delicate wall. + +In this way may be found a " Capillitium" (Fig. 4 op.), or net- +work of branch-like fine strands between the spores. Flowers of + + +B. Sporangium of Ar- +chidium candidum. +(a) open ; p wall of sporangium ; +(b) closed. + + +S +ALGAE. + +Tan (Fulgo spinos) has a fruit-body composed of many sporangia (see Althamium), which has the appearance of flat, irregular, brown cakes, inside the fragile external layer of which a loose powder, the spores, is found. It generally occurs on heaps of farmers' bark, and appears somewhat similar to Fulgo spinos, but that material is used, and is destructive by spreading itself over the bark and choking them. + +All the motile stages may pass into resting stages; the small forms only survive these without a wall, but the large ones at the same time divide in addition into polyhedral cells. When favourable conditions arise, the walls dissolve and the whole appears again as a naked (free-moving) mass of protoplasm. + +To the following genera belong: *Fulgo* spinosus, *Fulgo* spinosus, *Bryonema*, *Pleurococcus*, *Stenocaulon*, *Lycogala*, *Fulgo*, *Sporosira*, *Eotricaria*. + +Some genera wanting a sporangium-wall belong to the Slime-Fungi : *Cronartium*, whose fruit-body consists of polygonal plates, and is covered with a slime-like substance; and in the swarm-stage is wanting and which has stalked spores. *Phaeomorphophora braeica* prevails upon the roots of cabbages and other cruciferous plants, causing large swellings. *Pl. alba* causes severe ailments among root-growth on the roots of various plants. *Phylogymna leptophylla* may be found as small knobs (tubercles) on the roots of liraginuous plants. It is still uncertain whether it is this Funicus or Bacteria which is the cause of the formation of these tubercles. + +Sub-Division I. — ALGAE. + +**Mode of Life.** The Algae (except most of the Bacteria) are themselves able to form their organic matter by the splitting up of the carbonic acid contained in the water, or air in some cases, and for this purpose need light. The majority live in water, fresh or salt, but many are present on damp soil, stones, bark, etc., and in soil. + +With the exception of the Bacteria, no saprophytes have actually been determined to belong to this group, and only very few true parasites are known (e.g., *Pseudomonas*, *Algeria*, etc.), but good many are found epiphytic or endophytic on other algae or water plants, and on animals (for instance, certain Schizophryes and Protococcoides; Trichophyton weickeri in the hairs of Brugmansia and the Sthoth), and several species in symbiotic relation to various + + + + + +
9
+ +Fungi (species of Lichens), to Sponges (e.g. *Tentacellosa georgiop- +pala*, *Spongia delimitata*), and toundry Fungi and other +lower animals as Radiolaria, Hyphae, etc. (the so-called *Zoocystella* +and *Zoanellites*, which are perhaps purely stages in development +of various Green and Brown Algae). + +**Vegetative Organism**. The cells in all the Algae (excepting +certain unicellulars) are surrounded by a membrane which +(with the exception of the Bacteria) consists of pure or altered +cellulose, sometimes forming a gelatinous covering, at other times +a harder one, with deposits of chalk or albumen formed in it. The +membrane is often called the *plasmalemma*. In the Schizomycetes, +which are unicellular, may be one or more (e.g. *Hydrodictyon*, *Nephthea*) in each cell. Except- +ing in the majority of the Bacteria, colour materials (of which +chlorophyll, or modifications of it, always seems to be found) occur +in the cytoplasm, but not in the nucleus. In the higher Algae the cell- +nucleus, as in most of the coloured Schizophytes or are con- +tained in certain specially formed small portions of prodephasm +(chromatophores). + +The cells divide at a certain stage of development consist only +always of only one cell; by its division multicellular individuals +may arise, or, if the daughter-cells separate immediately after the +division, as in many of the simplest forms, the individual will, +during its further growth, become a multicellular organism with a single +cell (unicellular Algae). In multicellular individuals the cells +may be more or less firmly connected, and all the cells of the +individual may be exactly alike, or a division of labour may take place between them. The form of the cells is variable, and are +constructed accordingly; this may also occur in parts of the cell +in the large unicellular and multicellular Algae (Nephthea, p. 62). + +The cells in most of the Algae belong to the parenchymatous form; +those in some few to the collenchymatous form; and those in some +somewhat oblong; in many Algae (particularly Fucoidae and Florideae) +occur, moreover, Apkys-like threads, which are very long, +often branched, and are either formed of a single cell, or, more +frequently, of several cells united by their walls into a coenocytic growth. +The parenchymatous as well as the hyphal-like cells +may, in the higher Algae (especially in certain Fucoidae and +Florideae) be first differentiated, so that they form well- +defined and histologically distinct systems of tissue, e.g., assimilating, +conducting, storing, and mediating. + +With regard to the external form, the thallus may present no + +10 +A.G.E. + +differentiation, as in many multicellular Algae, or in multicellular Algae of the lower order, which are then either equally developed in all directions (e.g. Pleurococcus, Fig. 47), or form flat cell-plates (Mesophyllum) or threads (Ocularia, Fig. 21). The first step in the way of differentiation is the formation of a stem, leaf, shoot and base (Ricciaria, Porphyra); but the division of labour may proceed so that differences may arise between vegetative and reproductive cells (Eudogium, Fig. 54); hairs and organs of attachment being formed on one side of the plant, while the leaves at roots, are developed, and even leaves in certain forms of high order, belonging to different classes (e.g. Caulerpa, Fig. 50; Chironia, Fig. 61; Sargassum, Fig. 72; and many Florideae). + +The second step in differentiation is the formation of spores, in many instances, simply by division into two, and more or less complete separation of the divided product (Diatomeae, Desmidiaceae (Fig. 36), many Fucus-plants, etc.), or by detached portions of the thallus being set free as gametes (e.g. Rhodomonas, Rhodochloris, phycomyce, small filaments known as hormogonia are set free), or asexually by special reproductive cells (spores) set free from the thallus; these may be either stationary or motile. The stationary reproductive cells are called zoospores (e.g. Rhodochloris), and the motile ones (trapsores of the Floridean), or may possess a cell-wall; in the latter case they may be formed directly from the vegetative cells, generally by the thickening of the walls (kaikoule), or only after a process of division has taken place. The zoospores are either akinetes, as well as akinetes, may either germinate immediately or may become resting-cells, which germinate only after a period of rest. + +The spore-leaf reproductive cells are spherical, egg- or pear-shaped bodies (Fig. 58), which are produced by budding off from other cells (cooperation), and propel themselves through the water by means of cilia; or they are Pgylo-amoebae, which have no cilia and creep on a substratum by means of pseudopodia. The cilia, when present, are usually situated at the pointed end (though however, from the membrane), are mostly situated at the pointed and colourless end, which is directed forwards when in motion, and are 1 to 4 (Fig. 63 B), 4 or more. Both the cilia in the Brown Algae are usually situated at the pointed end (Fig. 64 A), and are usually situated in a circle round the front end (Eudogium, Fig. 6 A, and Desmoea), or are very numerous and situated in pairs dis- +tributed over a large part or nearly the whole of the sporocarp (Yezkoria). Besides being provided with one or more nuclei + +A.C.E. +11 + +(Fanacheta), they may also have a red "eye spot" and vacuoles, which are sometimes pulsating, etc. They appear and reappear at certain intervals. The swampsperes move about in the water in irregular paths, and apparently quite voluntarily, revolving round their longer axes; but they come to the surface, and then remain there until they are attacked by their dependence on light, or driven by some passing mass of food material. + +The swampsperes germinate, each forming a new plant, as their movements show. They surround themselves with a cell-wall, grow, and then divide into two parts, one of which is in the condition of germination, and about to attach themselves by means of the front end, which has been developed into haptera (see also Fig. 5 B, lowest figure). + +**Fig. 5.** Swampsperes germinative. A The lower cells are full of swampsperes, while the upper ones are empty. The greater part have escaped through the aperture m. of the cell-walls. + +**Fig. 6.** - Germinating swampsperes. + +The sexual reproduction here, probably in all cases, consists in the coalescence of two masses of protoplasm, that is, in the fusion of their nuclei. + +The swampsperes reproduce from autotomous conjugation, or isogamous fertilisation, and is characterized by the fact that the two coalescing cells (termed gametes) are equal, or almost equal, in shape and size (the female gamete in the Oultericon, e.g. Zanzaridinæ) + + +A: A close-up view of a swampsperes germinating. +B: A close-up view of a swampsperes germinating. +C: A close-up view of a swampsperes germinating. +D: A close-up view of a swampsperes germinating. +E: A close-up view of a swampsperes germinating. +F: A close-up view of a swampsperes germinating. +G: A close-up view of a swampsperes germinating. +H: A close-up view of a swampsperes germinating. +I: A close-up view of a swampsperes germinating. +J: A close-up view of a swampsperes germinating. +K: A close-up view of a swampsperes germinating. +L: A close-up view of a swampsperes germinating. +M: A close-up view of a swampsperes germinating. +N: A close-up view of a swampsperes germinating. +O: A close-up view of a swampsperes germinating. +P: A close-up view of a swampsperes germinating. +Q: A close-up view of a swampsperes germinating. +R: A close-up view of a swampsperes germinating. +S: A close-up view of a swampsperes germinating. +T: A close-up view of a swampsperes germinating. +U: A close-up view of a swampsperes germinating. +V: A close-up view of a swampsperes germinating. +W: A close-up view of a swampsperes germinating. +X: A close-up view of a swampsperes germinating. +Y: A close-up view of a swampsperes germinating. +Z: A close-up view of a swampsperes germinating. +AA: A close-up view of a swampsperes germinating. +AB: A close-up view of a swampsperes germinating. +AC: A close-up view of a swampsperes germinating. +AD: A close-up view of a swampsperes germinating. +AE: A close-up view of a swampsperes germinating. +AF: A close-up view of a swampsperes germinating. +AG: A close-up view of a swampsperes germinating. +AH: A close-up view of a swampsperes germinating. +AI: A close-up view of a swampsperes germinating. +AJ: A close-up view of a swampsperes germinating. +AK: A close-up view of a swampsperes germinating. +AL: A close-up view of a swampsperes germinating. +AM: A close-up view of a swampsperes germinating. +AN: A close-up view of a swampsperes germinating. +AO: A close-up view of a swampsperes germinating. +AP: A close-up view of a swampsperes germinating. +AQ: A close-up view of a swampsperes germinating. +AR: A close-up view of a swampsperes germinating. +AS: A close-up view of a swampsperes germinating. +AT: A close-up view of a swampsperes germinating. +AU: A close-up view of a swampsperes germinating. +AV: A close-up view of a swampsperes germinating. +AW: A close-up view of a swampsperes germinating. +AX: A close-up view of a swampsperes germinating. +AY: A close-up view of a swampsperes germinating. +AZ: A close-up view of a swampsperes germinating. +BA: A close-up view of a swampsperes germinating. +BB: A close-up view of a swampsperes germinating. +BC: A close-up view of a swampsperes germinating. +BD: A close-up view of a swampsperes germinating. +BE: A close-up view of a swampsperes germinating. +BF: A close-up view of a swampsperes germinating. +BG: A close-up view of a swampsperes germinating. +BH: A close-up view of a swampsperes germinating. +BI: A close-up view of a swampsperes germinating. +BJ: A close-up view of a swampsperes germinating. +BK: A close-up view of a swampsperes germinating. +BL: A close-up view of a swampsperes germinating. +BM: A close-up view of a swampsperes germinating. + +12 + +**ALGAE** + +**ciliaria**, Fig. 7, is considerably larger than the male gamete). The cell in which the gametes are developed is called a *gametangium*, and the reproductive cell formed by their union—which generally has a thick wall and only germinates after a short period of rest—is termed a *zygote* or *zygospore*. The conjugation takes place in two ways: + +(v) In the one way the gametes are motile cells (planktonic, zoospores), i.e., they swim in pairs during their swarming hither and thither in the water; during this process they first touch each other (Fig. 8 a), generally at first touching to the clear anterior end, and after a time they coalesce and become a zygospore (Fig. 8 b), which surrounds itself with a cell-wall (Fig. 8 c). + +This form of conjugation is found in *Ulothrix* and other Algae (Fig. 45, 56, 60). + +(b) Among other Algae (e.g. *Diatomeae* and *Conjugatae*), the conjugating cells continue to be surrounded by the cell-wall of the mother-cell (*aplospore*); the + + +A: A motile cell (zoospore) +B: A motile cell (zoospore) +C: A motile cell (zoospore) +D: A motile cell (zoospore) +E: A motile cell (zoospore) +F: A motile cell (zoospore) +G: A motile cell (zoospore) +H: A motile cell (zoospore) +I: A motile cell (zoospore) +J: A motile cell (zoospore) +K: A motile cell (zoospore) +L: A motile cell (zoospore) +M: A motile cell (zoospore) +N: A motile cell (zoospore) +O: A motile cell (zoospore) +P: A motile cell (zoospore) +Q: A motile cell (zoospore) +R: A motile cell (zoospore) +S: A motile cell (zoospore) +T: A motile cell (zoospore) +U: A motile cell (zoospore) +V: A motile cell (zoospore) +W: A motile cell (zoospore) +X: A motile cell (zoospore) +Y: A motile cell (zoospore) +Z: A motile cell (zoospore) +AA: A motile cell (zoospore) +BB: A motile cell (zoospore) +CC: A motile cell (zoospore) +DD: A motile cell (zoospore) +EE: A motile cell (zoospore) +FF: A motile cell (zoospore) +GG: A motile cell (zoospore) +HH: A motile cell (zoospore) +II: A motile cell (zoospore) +JJ: A motile cell (zoospore) +KK: A motile cell (zoospore) +LL: A motile cell (zoospore) +MM: A motile cell (zoospore) +NN: A motile cell (zoospore) +OO: A motile cell (zoospore) +PP: A motile cell (zoospore) +QQ: A motile cell (zoospore) +RR: A motile cell (zoospore) +SS: A motile cell (zoospore) +TT: A motile cell (zoospore) +UU: A motile cell (zoospore) +VV: A motile cell (zoospore) +WW: A motile cell (zoospore) +XX: A motile cell (zoospore) +YY: A motile cell (zoospore) +ZZ: A motile cell (zoospore) + + + +**Fig. 8.—Ulothrix zoosporæ; a portion of a thread with zoosporæ, of which two are formed in each mother-cell. The zoosporæ are shown in different stages of development. I, II, III, IV, V, VI, VII, VIII, IX, X, XI, XII, XIII, XIV, XV, XVI, XVII, XVIII, XIX, XX, XXI, XXII, XXIII, XXIV, XXV, XXVI, XXVII, XXVIII, XXIX, XXX, XXXI, XXXII, XXXIII, XXXIV, XXXV, XXXVI, XXXVII, XXXVIII, XXXIX, XL, XLI, XLII, XLIII, XLIV, XLV, XLVI, XLVII, XLVIII, XLIX, L, LI, LII, LIII, LIV, LVII, LVIII, LXI—LXIV. Ia—IVa—IVb—IVc—IVd—IVe—IVf—IVg—IVh—IVi—IVj—IVk—IVl—IVm—IVn—IVo—IVp—IVq—IVr—IVs—IVt—IVu—IVv—IVw—IVx—IVy—IVz—Vaa—Vaab—Vaac—Vaad—Vaabe—Vaabf—Vaabg—Vaabh—Vaabi—Vaabj—Vaabb—Ia—Ib—Ic—Id—Ie—If—Ig—Ih—Ii—Ij—Ik—Il—Im—In—Io—Ip—Iq—Ir—Ii—Ij—Ik—Il—Im—In—Io—Ip—Iq—Ir—Ii—Ij—Ik—Il—Im—In—Io—Ip—Iq—Ir—Ii—Ij—Ik—Il—Im—In—Io—Ip—Iq—Ir—Ii—Ij—Ik—Il—Im—In—Io—Ip—Iq—Ir—Ii—Ij—Ik—Il—Im—In—Io—Ip—Iq—Ir-Iii-Iiv-Ivi-Ivj-Ikv-Ilw-Iix-Iiy-Iiz-Ilia-IIib-IIic-IIid-IIje-IIkf-IIkg-IIlh-IIji-IIkj-IIkk-IIlj-IIkl-IIlk-IIll-IIml-IImn-IIno-IIpp-IIpq-IIqr-IIrs-IIss-IItu-IItv-IIuw-IIvx-IIwy-IIxz-IIIaa-IIIab-IIIac-IIIad-IIIae-IIIaf-IIIag-IIIah-IIIai-IIIaj-IIIak-IIIal-IIIam-IIIan-IIIao-IIIap-IIIaq-IIIar-IIIas-IIIbt-IIIct-IIIdd-IIIde-IIIdf-IIIge-IIIhh-IIIhi-IIIij-IIIjk-IIIkl-IIIll-IIIma-IIImb-IIImc-IIImd-IIIme-IIImf-IIImg-IIImh-IIImi-IIImj-IIImk-IIIml-IIImm-IIImo-IIImp-IIImq-IIImr-IIIms-IIImt-IIInu-IIIod-IIiee-IIiff-IIigg-IIihh-IIijj-IIikk-IIill-IIimmm-IIinii-IIjnjj-IIikkk-IIilll-IIimmm-IIinii-IIjnjj-IIikkk-IIilll-IIimmm-IIinii-IIjnjj-IIikkk-IIilll-IIimmm-IIinii-IIjnjj-IIikkk-IIilll-IIimmm-IIinii-IIjnjj-IIikkk-IIilll-IIimmm-IIinii-IIjnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-Iikkk-Iilll-Iimmm-Iinii-Ijnjj-iikkk-iilll-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii-injj-iikkk-illl-immm-inii—in jj-iikk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill-limm-lnn-j-jk-kk-lill- + + +**Fig. 9.—Ulothrix zoosporæ; a portion of a thread with zoosporæ of which two are formed in each mother-cell. The zoosporæ are shown in different stages of development. Ia–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv–Iv– + +**Fig. 10.—Ulothrix zoosporæ; a portion of a thread with zoosporæ of which two are formed in each mother-cell. The zoosporæ are shown in different stages of development. Ia – Ib – Ic – Id – Ie – If – Ig – Ih – IIa – IIb – IIc – IID – IIe – If – Ig – Ih – IIa – IIb – IIc – IID – IIe – If – Ig – Ih – IIa – IIb – IIc – IID – IIe – If – Ig – Ih – IIa – IIb – IIc – IID – IIe – If – Ig – Ih – IIa – IIb – IIc – IID – IIe – If – Ig – Ih – IIa – IIb – IIc – IID – IIe – If – Ig – Ih – IIa - + +A.I.G. 13 + +Aplanogametangia generally grow out into short branches, which lie close together and touch one another, the wall at the point of contact then dissolved (Fig. 30). Through the aperture thus formed, the aplanogametes unite, as in the first instance, and form a rounded zygote, which immediately surrounds itself with a cell-wall. Various modifications occur; compare Figs. 37, 38, 41, 43. + +The highest form of the sexual reproduction is the Egg or Oogamous fertilization. The two coenocytic cells are in the main alike each other in form, well as in size. The one which is con- +tained in the egg-cell is known as the egg-spermatozoon (spermatozoa), develops as a rule a large numbers in each mother-cell (autolysis). + +A B C D E F G H I J K L M N O P Q R S T U V W X Y Z +Fig. 30.—Fertilization in the Helioblastum (Pseus reticulatus). + +diem); they are often self- +mottle (except in the Flori- +dian species, which are named +sporophores), and are some- +times smaller than the other +kind, the female, which is +known as the egg-cell +(sporophore). The egg-cell is +always a motionless, spherical, +primordial cell which can either float about freely in the +water, as in the Fucusia (Fig. 9), or is surrounded by a cell-wall +(孢子囊), generally only one sporophore is to be found in each +oogonium, but several occur in Sphagnum (Fig. 10). The re- + +14 +A.G.R. + +silt of the spermatocorm coalescing with the egg-cell is, as in the preceding case, the formation of a zygote, which generally undergoes a period of rest before germination (the Florideae are an exception, a fruit-body, cytopsyr, being produced as the result of coalescence.) + +An excentric fertilization is effected by the Algæ. Sphaerocoryne (Fig. 8). The filamentous thallus is formed of cylindrical cells with many vacuoles (r in A); some cells divide egg-cells (B), others spermatocysts (C), the latter in a parenchymatous layer. The egg-cells are surrounded by a cell-wall or a club-elongate paracyste with two ellips at the front end (G). It is however a swimmers. The spermatocysts come from their cells through apertures in the wall of the paracyste. The spermatozoa swim out through these apertures. The columnar end of the spermatocorm is united at first with the "re- sive spout" of the egg-cyst (H). Then the formation of a zygote with water takes place (I). + +The female (parthenogenetic) or male (androgenic) sexual cell may, sometimes without any preceding fertilization, form a new individual (e.g. *Ulotheca somata*, *Ojentrocarpus*, etc.). + +**Systomata** **divisoria** of the Algæ. The Alge are divided into the following classes: + +1. **Syngeneutaceae**, Dinoecellulaceae, or Peridinaceae. 3. Diatom- +aceae; 4. Scourghitidae, Fissos.-ageae; 5. Conjugatae; 6. Chloro- +phyceae, Gymnox.-ageae; 7. Chlorella, Stenostyphus; 8. Phycophyceae; +9. Dictyotales; 10. Rhodophytae. + +Among the various forms of the Algæ, the Syngeneutaceae, the Dinoflagellata, and the unicellular Volvocinean (Chlamydomonade), distinct transitional forms are found approaching the animal kingdom, which can be grouped as animals or plants according to their mode of life, taking food or other characteristics. Only an artificial boundary has been drawn between the animal and vegetable kingdoms. In the following pages only those forms which possess chromatophores, and have no mouth, will be con- +sidered as Algæ. + +Class I. **Syngeneutaceae**. + +The individuals are uni- or multi-cellular, free-swimming or motionless. The cells (which in the multicellular forms are loosely connected together, often only by mucilaginous envelopes) are naked or surrounded by a mucilaginous cell-wall, in which silicon is never embedded. They contain one cell-nucleus, one or more pulsating + +STENOGONIA. +vacuoles, and can to two hand, or plate-like chromatophores with a brown or yellow colour, and sometimes a greenish hue. + +Reproduction takes place by vegetative division, or axenically by zoospores, akinetes (or aplanospores?). Sexual reproduction is un- +known. They are all fresh water forms. + +To this class may perhaps be assigned the recently arranged and very little known genus *Stenogonia* (Dichotomocera), which partly occur in the free condition in the sea, in the so-called "sea-eggs", and which are symbiotic in various lower marine animals. + +The *Sympathecium* are closely re- +lated to certain forms in the animal +kingdom, as the Flagellate. + +Order I. Chrysoomonadinae. In +divisional stages, the cells, remain- +ing in free condition, naked or sur- +rounded by a multinucleated covering. +The cell is usually ovoid or ellipsoid, +2 (rarely only 1) cilia, almost of the same length, and generally with a radial "eye-spot" at their base, and with 3 (rarely 2) nuclei. The division of the individual cells either during the streaming, or during a resting stage, is effected by liberation of one or more cells, which in the latter case are connected together. + +A. Unicellular: Chrysoamonas, Cryptomonas, Micromonas, Neoproteus. + +B. Multicellular: *Chrysochromatium*, *Chrysochromatium*. + +Among the unicellular Chrysoomonadinae are probably classified some forms which are only stages in the development of the multinucleate, or of other species. + +Order II. Chrysopyaceae. Are unicellular, and differ mainly from the pre- +ceding in being attached either on a slime-thread (Spilis- +thrix), or on a stalk (Eucyamnus). + +They have two cilia, and multiply by longitudinal (Gymnodinium) or transverse (Chrysophyceae) division of one of the daughter-individuals (zoospore). Division may also take place in a motilecute stage (pseudocyst-stage). +Only one nucleus is present in each cell. The cells are gen- +tially attached, uni- or multi-cellular; each individual cell is distinctly contractile, and fixed at the bottom of a gelatinous sheath. + +Fig. 15.—Sympathecium: the multi- +nucleate individual is surrounded by a +multinucleated granular envelope. + +Order III. *Sympathecium*. The cells are attached to each other by means of a +gelatinous sheath. The cells are multinucleate; they are +contractile, and move by means of cilia. They are +planktonic organisms. + +*Sympathecium*, *Dimorphom** + +16 + +**DINOFLAGELLATA.** + +Order 4. **Hydracria.** The individuals are attached, without cilia, multi- +cellular, branched, and with apical growth. The cells are spherical, but in the final stage they become elongated, and finally break up into multinucleate. Asexual reproduction by zoospores which are tetrahedral, with 1 cella, and by resting akinetes. *Hydracria* is common most in mountain brooks. + +Class 2 **Dinoflagellata.** + +The individuals are of a very variable form, but always uni- +cellular, and floating about in free condition. The cell is dorsi- +central, bilateral, asymmetrical and generally surrounded by a colour- +less membrane, which has no stolae embedded in it, but is formed of a substance which is more or less transparent. The body is rectan- +gularly provided with pores and raised borders, easily breaks up into irregularly-shaped pieces. In the forms which have longitudinal and cross furrows, two cells are fixed where these cross each other, and project their anterior extremities towards the front of the body perpendicu- +larly and is directed longitudinally to the front or to the rear, the other one stretches acrosses and lies close to the cell, often in a narrow (cross furrow). The chromatophores are coloured brown or green. In some cases they are yellowish or orange-coloured. They are radially placed, discs, which sometimes may coalesce and become a star-shaped chromatophore. The colouring material (pyrophyll) consists, in addition to a modification of chlorophyll, also of phycoglycine and phycoside. The food is obtained by the products of assimilation which consist of yellow, red or colourless oil (?) and starch. Cell-nucleus one: In *Pseudofulvella* several nuclei are found; contractile vacuoles many, which partly open in the ciliae (?). (Fig. 10.) In some case oocytes, coloured red by haematochrome. For the *Pyrophyllinae* see pagenote in *Euglenida.* + +The reproduction takes place as far as known at present, +only by division. This is many times the form that takes +place in the swarming condition, and in that case, is always +parallel to the longitudinal axis. The daughter-individuals, each of which retains half of the original shell, sometimes do not separate +at once from each other (Fig. 11), but remain connected (e.g., Fig. +12). In this case several connected individuals may be formed. In others, +the division occurs after the cilia have been thrown off and the cell-om- +tentis rounded. The daughter-cells then adoptively new cell-walls. +A palaeola-la-stage (motional division-stage) sometimes appears to + +DUXOPLACELLA. 17 + +take place, and also phaneropores (?) with one or two burn-like elongations (e.g. in *Peridinium cinctum* and *P. tubulatum*); at germination one, or after division two or more new individuals may be formed. + +Sexual reproduction has not been observed with certainty. + +The Bacteria move forward or backward, turning round their longitudinal axes; in their motion they are influenced by the action of light. The motion possibly may be produced only by the transverse cilia, which vibrate rapidly; whilst the longitudinal cilium moves slowly, and is supposed to serve mainly for the appearance that they live principally in salt water, but also in fresh. + +Besides the coloured forms, which are not dependent on their own organic compounds by the splitting up of the carbonic acid contained in the water, there are a few colourless forms (e.g. *Gymnodinium*, etc.), or those which possess chromatophores (*Pelagia*); these appear to live saprophytically, and may be able to absorb solid bodies with which they come into contact. + +Diatomaceae are found in the "Plankton" of the open sea, where they form together with Diatomaceae the basis for the known life. It is known that every community that lives in the sea is furnished with food (like the Nautilius, which belongs to the animal kingdom and to which they are perhaps related) produce light, known as bioluminescence. + +Diatomaceae (*Cyclotella, Cyclotilium*) are allied through their lowest form (Cyclocyclus) to the Synechococcus, which have no chloroplasts. They may be divided into three orders. + +Order I. *Cyclotella*. With numerous and generally longitudinal furrows. Many radially placed, disc-forming chromatophores. The most common genera are: + +- *Cyclocyclus* (Fig. 13), *Peridinium*, *Gymnodinium*, *Dinophysis*, *Chlorodinium*, *Pelagia*. +- With several transverse furrows, no chromatophores, and several chlorophylls. Only one genus: *Pelagia*. + +A diagram showing the structure of a diatom cell. +Fig. 13.—A diatom cell.
+18 A. The cell wall with its various
+19 ails. B from behind: 1st transverse
+20 furrow; 2nd transverse furrow;
+21 chloroplasts; e starch; y reticulum;
+22 C cytoplasm from the vesical
+23 membrane; d nucleus; f longitudinal
+24 furrow; g chloroplast; h chlorophyll; i
+25 transverse furrow; p chloroplasts
+26 within the vesicle; q longitudinal
+27 furrow; r chloroplasts within the
+28 vesicle; s chlorophyll; t chloroplasts
+29 within the vesicle; u chlorophyll; v
+30 transverse furrow; w chloroplasts
+31 within the vesicle; x chlorophyll; y
+32 transverse furrow; z chloroplasts
+33 within the vesicle; a chlorophyll;
+ +Order II. *Pelagia*. With several transverse furrows, no chromatophores, and several chlorophylls. Only one genus: *Pelagia*. + +Order III. *Gymnodinium*. With numerous and generally longitudinal furrows. Many radially placed, disc-forming chromatophores. The most common genera are: + +- *Cyclocyclus* (Fig. 13), *Peridinium*, *Gymnodinium*, *Dinophysis*, *Chlorodinium*, *Pelagia*. +- With several transverse furrows, no chromatophores, and several chlorophylls. Only one genus: *Pelagia*. + +Order IV. *Gymnodinium*. With numerous and generally longitudinal furrows. Many radially placed, disc-forming chromatophores. The most common genera are: + +- *Cyclocyclus* (Fig. 13), *Peridinium*, *Gymnodinium*, *Dinophysis*, *Chlorodinium*, *Pelagia*. +- With several transverse furrows, no chromatophores, and several chlorophylls. Only one genus: *Pelagia*. + +18 +DIATOMEE. + +The order *Pseudodinacea* deviates to a high degree from the other Dinoflagellata, not only by its many transverse furrows, each with its own transverse ellipsoid, and by the absence of a median furrow, but also by the presence of a second kind of flagellum, which otherwise does not occur within the whole class. It may therefore be questionable whether this order should really be placed in the vegetable kingdom. + +Class 3. Diatomacee. + +The individuals of this class are unicellular organisms, assume very various forms and may be unicellular or multicellular, but present no differentiation; many similar cells may be connected in chains, embedded in mucilaginous masses, or attached to mucilaginous stalks. The cells are usually disc-shaped, elliptical or oval, slightly dipcentral and have no cilia; those living in the sea condition have the power of sliding upon a firm substratum. The cell contains 1 cell-nucleus and 1–2 plate-shaped or several disc-shaped chloroplasts. The latter contain a large amount of chlorophyll, in addition to a modification of chlorophyll, a brown colouring matter, diatomin. 1 or 2 pyrenoids sometimes occur. Starch is wanting and the first product of assimilation appears to be a kind of oil. + +The cells are impregnated with silica to such a degree that they are imperishable and are therefore able to contribute in a great measure to the formation of the earth's crust. The structure of their cut-edges is most peculiar and differs from that of plants (except for the *Chlorophyceae*, which do not possess a single nucleus, but is made up of two—the "shells"—compare *Eucnella* and *Proconchium* among the Dinoflagellata) which are fitted into each other, on one side forming a kind of hinge-like joint, like a box with its lid (Fig. 14 B). The two parts which corre- +19spond to the bottom and lid of the box are known as valves. +Along the central line of the valves a longitudinal rib may often be found, interrupting at its course into a small cleft (perichora homologous with the perichora of the Dinoflagellata), through which the protoplasm is enabled to communicate with the exterior (Fig. 14 A). It is principally by reason of the valves, which bear numerous, transverse striae, strim or warts, etc. (Figs. 14, 16, 17), that the Diatomaceae are easily distinguished from other algae as test objects in microscopical science. When the division takes place, the two shells are separated a little from each other, and after the cell-contents have divided into two masses, two new shells are formed, one fitting into the larger valve, the other one + +Diatomeae. 19 + +into the smaller valve of the original frustule. The latter cell (frustule) is thus, upon the whole, smaller than the mother-cell, and as the cells do not increase in size, some frustules are smaller than the ones fructifying, and these are produced by repeated division; it follows that smaller and smaller frustules are pro- +duced. This continued diminution in size is, however, compensated for by the fact that the valves of those have been reduced to a certain minimum, of anapogres, 2–3 times larger. These may easily be recognized by the +prolapse of a cell inclosing, round- +ing off and surrounding itself with a +new wall (e.g. Meloira) or after con- +jugation, which may take place with +various degrees of difficulty. Indi- +viduals unite after the secretion of a +quantity of mucus, and the valves then commence to separate from each other, so that at first the two indi- +viduals turn towards each other. The + +Fig. 14.—Pinacodermis: $R_1$ from +the edge, shows the valves fitting +together; $A$, a valve. + +Fig. 15.—Various Diatomaceae: A Diatoma vulgaris. B Nitzschia expansa. C Nitzschia +tenuis (internal view). D Gonyaulax ascerticula (external view). E Nitzschia ussii +(external view). + +protoplasmic bodies now release themselves from their cell-wall, +and each rounds off to form an ellipsoidal mass; these two pro- + +20 +Diatomeae. + +toplasmic masses (gametes) coalesce to form a zygote, the cell- +nuclei and chromatophores also fusing together. The zygote in- +creases in size, and surrounds itself with a firm, smooth, siliceous +wall—the perizonium. The auxospores, whichever way they arise, +are not resting stages. The germination of the zygotc com- +mences by the expulsion of the protoplast from the wall, which +is cell-wall and constructing first the larger valve, and later on +the smaller one; finally the membrane of the zygotc bursts (e.g. +Haustratium). 2. The conjugation occurs in a similar manner, +but the zygotes are not formed into two daughter-cells, but by +conjugation into two daughter-cells. Those lying opposite one +another conjugate (Fig. 16) and form two zygotes. The for- +mation of the perizonium, and germination take place as in the +preceding instance (e.g. *Euplottia*). 3. Two cells placed close- +to each other, and one of the two effecntons, + +A B C D + +Fig. 16.—Conjugation of *Cymbella varicella*. A, The protoplasts in the two cells be- +dividing into two masses; B those masses coalesce in pairs; the cells (f) coalesced in a +massive condition; C, D, Two cells placed close together. + +without coalescing, becomes an auxospore. The formation of +the wall takes place as in the preceding case. This is found in +the Naviculaceae, and in the *Complanaceae* (e.g. *Fratellina, +Coconoea*). + +The Diatomaceae may be found in salt water as well as in fresh water +(when in such masses that the colour of the water or mud becomes +yellow or brown); in the same manner the genera *Chetoneura, +Elodeococcus, Coscinodiscus*, and several others, form large silime- +masses, "Phankton" on the surface of the sea), on damp soil and in dust. In fresh water they are often found in great accumu- +lations, often in large deposits (siliceous earth, mountain +meal), as in the cement lime in Jutland, the alluvial deposits +beneath Berlin, in clay strata beneath peat bogs, in grano, etc. + +DIATOMEAE. +21 + +These accumulations of fossilized diatoms are used in the manu- +facture of dynamite and in various manufactures. + +The Diatomeae appear nearest to, and must be placed as a group co-ordinate with the Dinoflagellata, as they doubtless may be supposed to derive their origin from forms resembling *Eucariota*, an hypothesis which is supported by the numerous analogies which are striking in many respects, can only be conceived as analogies, and cannot be founded upon homologies, and it is therefore impossible to regard them as proof of genetic relation- +ship. The family contains only one order. + +Order 1. Diatomacea. This order may be divided into two sub-orders, viz: + +Sub-order 1. *Placochromatica*. The chromatophores are discoid, large, 1 or 2 in each cell; the structure of the valves is bilateral and always without reticulate markings. The follow- +ing groups belong to this sub-order: *Gonophyenea*, *Cymbulites*, *Anachrysis*, *Pleurophycus*, *Pleurocystis*, *Pleurostomus*, *Pleurostomoides*, *Anaphthropus*, *Nitzschia*, *Surinamia*, and *Emotion*. + +Sub-order 2. *Coccochromatica*. The chromatophores are granular, small and many in each cell. The structure of the cells is similar to that of the preceding sub-order. The following groups belong to this sub-order: *Fragilaria*, *Meridion*, *Tubellaria*, *Lemnophora*, *Biddulphus*, *Anguliferus*, *Repullosa*, *Coccolodaceae* and *Melosira*. + + +A: A species of diatom. +B: A species of diatom. +C: A species of diatom. +D: A species of diatom. +E: A species of diatom. +F: A species of diatom. +G: A species of diatom. +H: A species of diatom. +I: A species of diatom. +J: A species of diatom. +K: A species of diatom. +L: A species of diatom. +M: A species of diatom. +N: A species of diatom. +O: A species of diatom. +P: A species of diatom. +Q: A species of diatom. +R: A species of diatom. +S: A species of diatom. +T: A species of diatom. +U: A species of diatom. +V: A species of diatom. +W: A species of diatom. +X: A species of diatom. +Y: A species of diatom. +Z: A species of diatom. +AA: A species of diatom. +AB: A species of diatom. +AC: A species of diatom. +AD: A species of diatom. +AE: A species of diatom. +AF: A species of diatom. +AG: A species of diatom. +AH: A species of diatom. +AI: A species of diatom. +AJ: A species of diatom. +AK: A species of diatom. +AL: A species of diatom. +AM: A species of diatom. +AN: A species of diatom. +AO: A species of diatom. +AP: A species of diatom. +AQ: A species of diatom. +AR: A species of diatom. +AS: A species of diatom. +AT: A species of diatom. +AU: A species of diatom. +AV: A species of diatom. +AW: A species of diatom. +AX: A species of diatom. +AY: A species of diatom. +AZ: A species of diatom. +BA: A species of diatom. +BB: A species of diatom. +BC: A species of diatom. +BD: A species of diatom. +BE: A species of diatom. +BF: A species of diatom. +BG: A species of diatom. +BH: A species of diatom. +BI: A species of diatom. +BJ: A species of diatom. +BK: A species of diatom. +BL: A species of diatom. +BM: A species of diatom. +BN: A species of diatom. +BO: A species of diatom. +BP: A species of diatom. +BQ: A species of diatom. +BR: A species of diatom. +BS: A species of diatom. +BT: A species of di atom +BU: +BV: +BW: +BX: +BY: +BZ: +CA: +CB: +CC: +CD: +CE: +CF: +CG: +CH: +CI: +CJ: +CK: +CL: +CM: +CN: +CO: +CP: +CQ: +CR: +CS: +CT: +CU: +CV: +CW: +CX: +CY: +CZ: + +Fig. 17.—Various Diatomeae. *A* Synecha rufina. *B* Rhizotheca torula (from the two different sides). *C* Pinnularia sp. (from the upper side). Light several times on a portion of a plant, on the left a single one more highly magnified. + +32 + +**Schizophyta** + +**Class 4. Schizophyta. Fission-Algae.** + +The individual cells are usually divided; the thallus consists in many of a single cell, in others of chains of cells, the cells dividing in only one definite direction (Figs. 18, 21). In certain Fission-Algae the cell-chain branches (Fig. 30) and a difference between the anterior and posterior ends of the chain is marked; in some, the cells may be united by a common wall, but in others the division takes place in two directions; and in others there are somewhat culi- nate masses, or rounded lumps of a less decided form, by the divisions taking place in three directions; or less defined masses may be formed by the lateral fission taking place at right angles. + +The cell-walls rarely become cellulose, they often swell considerably (Figs. 20, 22), and show distinct stratifications, or they are almost completely changed into a mucilaginous mass in which the protoplasts are suspended (Fig. 22). In some cases this condition is wanting. Vegetative reproduction by division and the separation of the divisional products by the splitting of the cell-wall or its becoming meconucleated; among the Nostocaceae, Lyngbyaceae, Synechococcales, Heterococcaceae, and other genera of Schizophytae, and others single reproductive akinetes are formed. Many Fission-Algae conclude the growing period by the formation of resting akinetes or aphanospores. + +The Schizophytae may be divided into two families: + +1. **Schizophyceae.** + *Family* Schizophyceae. + *Blue Green Algae.* + +All the Blue-green Algae are unicellular organisms, with means of a colouring material containing chlorophyll (chlorophyll I); but the chlorophyll in this substance is masked by a blue (phycoeyanin), or red (phycoerythrin, e.g. in Trichodesmium erythraeum in the Red Sea) colouring matter; this colouring matter is lost when the algae die and water after death. The colouring matter, in most of them, per- mutes the whole of the protoplasm (excepting the cell-nucleus), but in a few (e.g. Gloeocystis, Phycosphaera), slightly developed chromatophores are present. In some genera (e.g. *Chroococcus*, *Cyanidium*) filaments (cell-nucleus) a differentiation into apex and base (*Bacillariaceae*) may take place, and also between ordinary vegetative cells and heterocytes; these latter cannot divide, and are dis- + *Mylophycaceae*. Cyanophyceae. + +A diagram showing the structure of a Schizophytae cell. + +SCHIZHEMEL 23 + +tinguished from the ordinary vegetative cells (Fig. 22 b) by their larger size, yellow colour, and poverty of contents. Branching sometimes occurs and in either true or apuric. + +A diagram showing the structure of a filament. +**Fig. 16.** —Microcystis *syphogener*: a portion of a filament, the thick sheath enclosing only one cell-chain; in one place a cell is drawn out by the movement of the cell-chain is the other side of the filament, so that two filaments are formed, which are separated from each other. + +The cell-chain in the anterior branching divides into two parts, of which either one or both grow beyond the plane of division (Fig. 18) and often out to both sides (e.g. *Sympenema*), the divisions however, always take place transversely to the longitudinal direction of the cell-chain. In the true branching a cell elongates and then grows transverse to the cell-chain, and the division then takes place nearly at right angles to the former direction (*Simophyton*). + +A diagram showing the structure of a resting alomite with heterocysts and new heterocysts forming. +**Fig. 17.** —*Colletotrichum major*: a resting alomite with heterocysts; b d posteriorly arising from a resting alomite; c filaments with two heterocysts and the formation of new heterocysts; f part of a filament with a heterocyst, and mature resting alomites. + +Cilia are wanting, but the filaments are sometimes self-motile (or locomotive) and may be rapidly turned round their axes, partly slide forward or backward (*Oedogonium*). + +Reproduction takes place by spores and hormogonia in addition. + +24 + +**SCHIZOPHYTA** + +to simple cell-division. Hormogonia are peculiar fragments of a cell-chain capable of motion, and often exhibit a vigorous motion in the sheath, until at last they escape and grow into a new individual (Fig. 18). The spores are reproductive akinetes (Chromatium), which are formed by the division of the vegetative cells enlarging and constructing a thick cell-wall (Fig. 19 c-f). On permination, this cell-wall bursts and the new cell-chain elongates in the same longitudinal direction as before (Fig. 19 b c). Many (e.g., Ochromonas) produce akinetes in their ordinary vegetative state. Aplanoplasmae are wanting. + +The Fission-Acini are very prevalent in fresh water and on damp soil, less so in salt water; they also occur in water which almost never freezes, but they are found in warm spring with a temperature as high as 50° C. + +The Family may be divided into 2 sub-families: + +1. **Heterocystes (heterocysts are wanting)**: *Chroococcaceae*, *Lymphodiscus*, *Lithothrix*. + +2. **Heterocystes (heterocysts present)**: *Nadecocaceae*, *Etimo-araceae*, *Septomonas* and *Sirreiphomycetes*. + +Order 1. **Chroococcaceae**. The individuals are—many-celled, but all the cells are uniform, usually spherical or platelike or globular masses, often surrounded by a mucilaginous cell-wall, but never forming cell-chains. Multiplication by division and symmetrical fission is rare, but reproductive akinetes are wanting. + +*Chroococcus*, *Aphanocapsa*, *Gloeococcus* (Fig. 20), *Calophyton*, *Merismopodium*, *Oscillaria*, *Candea*, *Coryne*, *Polygymnia*, *Gymnothorax*. + +Order 2. **Lyngbyaceae** (*Oscillariaceae*) (Fig. 21). + +The cells are discoid (Fig. 21), united to straight or slightly curved filaments, which are unbranched, or with sparsious branching. The ends of the cell-chains are similar, but the terminal one is distinct by asymmetrical resting akinetes being wanting. *Oscillaria* (Fig. 21), *Spirulina*, *Lyngbya*, *Microcoleus*, *Symphonie*, *Pleotoma*. + +25 + +Order 3. *Chamaephonaceae.* The individuals are 1- +nucleated, attached, unbranched filaments with differentiation into apex and base; without heterocysty. Multiplication by re- +productive akinetes; resting akinetes are wanting. *Dermosporus, +*Clastidium*, *Chamomiphon*, *Golovinella*, *Phragmoneumus*. +Order 4. *Rivulariaceae.* The individuals are composed of mul- +ticellular, unbranched filaments, without differentiation into apex and base; heterocysts present. Reproduction by synkinetes and resting akinetes. + +Some genera are not macrogynous, e.g. *Cylindropermann* (Fig. +19). The cell-chains in others, e.g. *Nostoc*, wind in between one + +A small illustration showing a plant-like structure with a central rod-like body and branches extending outward. +Fig. 18.—*Nostoc* verrucosum. A. The plant in its natural size; b an irregularly folded +hollow mass. B. One of the multicellular enlargements, with its heterocysts (A), embedded in +its multinucleate sheath. + +another and are embedded in large structureless jelly-like masses, +which may attain the size of a plum or even larger (Fig. 22); sometimes they are attached to other plants or to rocks by filaments attached to other bodies. Other genera as follows: *Aphaniz- +monas* and *Anabaena* (in lakes and smaller pieces of water); *Nudobius* is partly pelagic. Some occur in the intercellular spaces of the leaves of *Equisetum*. These *Nostoc-forms* are found in *Anthoceros*, +*Elionia*, *Sphagnion*, *Lemna*, in the roots of *Equisetum* and *Pteris*; +*Anabaena* in Azolla. + +Order 5. *Rivulariaceae.* The individuals are multicellular +filaments with differentiation into apex and base, and spurious +branching and a heterocyst at the base of each filament. Re- +production by synkinetes and resting akinetes, rarely by simple +reproductive akinetes. *Rivularia*, *Glaucocystis*, *Incerta*, *Calothrix*. + +Order 6. *Secotytonaceae.* The individuals are composed of +multicellular filaments with no longitudinal division; differenti- +ation into apex and base very slight or altogether absent; + +Schizophysida + +26 BACTERIA. +branching spores ; heterocysts present. Reproduction by ana- +kinetes, rarely by resting akinetes and ordinary reproductive +akinetes. Telosporia, Systenoma, Hassula, Microchaete. +Order 7. Sirophoraceae. The individuals are formed of +multicellular threads with longitudinal division ; true branching +and Metachrona are wanting. Reproduction by apex and base. +Reproduction by akinetes, rarely by resting akinetes +and ordinary reproductive akinetes. Hapalosiphon, Stigomena, +Cyanobrya, Nostotrichia, Multigloeus. + +Family 2. Bacteria.* + +The Bacteria (also known as Schizomyces, and Fission-Fungi) are the smallest known organisms, and form a parallel group to the Blue-green Algae, but separated from these Algae by the absence of their colouring material ; chlorophyll is perhaps found in a few cases in some of the Bacteria. + +The various forms under which the vegetative condition of the Bacteria appear, are termed as follows : +1. Globular forms, coiçi (Figs. 27, 30 c): spherical or ellip- +soidal, sometimes with a central nucleus loosely massed together and generally termed "Micrococcus". +2. Rod-like forms : more or less elongated bodies ; the shorter forms have been styled "Bacterium" (in the narrower sense of the word), and the term " Bacillus" has been applied to longer forms +of similar nature ; the longer forms are long, straight and cylindrical (Figs. +28, 29, 30 E). +3. Thread-like forms : unbranched, long, round filaments, resembling those of *Oscillatoria*, are pos- +sible (very thin, non-grana- +lar filaments : Fig. 30 +A, short small filaments) +filaments, with strong, refractile grains or drops of sulphur (Fig. +* The Bacteria are more usually included under Fungi. It seems better, how- +ever, to place them under the Algae in a separate class with the Schizomyces. + +Fig. 25.-Spirillum sphaerulum. Four specimens. One has two cells at the same end, the sulphur granules are seen internally. + +BACTERIA. 27 + +31; often self-motile). Branched filaments, with false branching like many *Sporangiophora*, are found in *Gladiolus* (Fig. 30 B, G). + +4. *Spiral forms*: Rod-like or filamentous bodies, which more or less strongly resemble a corkscrew with a spiral rising to the left. In general these are termed *Spirula* (Fig. 23); very attenuated forms are known under the name of *Vorticella* (Fig. 30 D). Of these, the elements are slender and flexible with a closely wound spiral (*Spirochaete* (Fig. 24). + +5. The *Mycetobacteria*, consisting of rounded cells arranged in one plane, generally in groups of four, and produced by divisions perpendicular to the plane. + +6. The *Saccharomyces*, consisting of roundish cells which are produced by cellular divi- +sion, and all the three divisions of spores being into globular or ovoid masses ("parcels") e.g. *Saccharum* centriculii" (Figs. 28, 29). + +All Bacteria are unicellular. In the case of the micrococci this is self-evident, but in the "rod" "thread", and "spiral" Bacteria, very often numerous cells remain united together and their individual elements can only be recognised by the use of special reagents. + +Fig. 31.—Bacillus centriculii. One surr. +roundish cell, surrounded by a double contour, +which are drawn with double contour are more +distinctly than those cells lying deeper +drawn with single contour. + +Fig. 32.—Micrococcus minuta: a & d—successive stages of one individual (from a to d p.m.), f an individual of 2f cells. + +The common name "Zoogloea", which reminds us of *Nostoc*, is probably given by the cells being so closely packed that the number of individuals in active division are found embedded in a mass of mucilage, which either contains only one, or sometimes more, of + +28 + +**EACTERIAL** + +the above-named forms. The individuals may eventually swarm out and continue their development in an isolated condition. Such mucilaginous masses occur especially upon moist vegetables (potatoes, etc.), on the surface of fluids with decaying raw or cooked meat, and on the surface of water. They form minute int- +folds when the Bacteria, with their mucilaginous cell-walls, multiply so rapidly that there is no more room on the surface of the fluid. + +The cells of the Bacteria are constructed like other plant-cells in so far as their diminutive size has allowed us to observe them. The cell-wall only exceptionally shows the reactions of cellulose (in *Saccharum*, Lecanomus; also in a Vigna-bacterium, *Bacterium glycogenes*). The protoplasm is usually very thin. The body of the cell mostly appears to be an uniform or finely granu- +lated protoplast. Very few species (e.g. *Bacillus viscosus*) contain chlorophyll; others are coloured red (purple sulphur Bacteria); the majority are colourless. The cell-walls are often impregnated with a starch-like material when treated with iodine before the spore-formation. Some Bacteria contain sulphur (see p. 37). The body, which has been described as a cell-sacculus, is still of a doubtful nature. + +Artificial colourings with aniline dyes (especially methyl-violet, gentian-violet, methylene-blue, fuchsin, Bismark-brown and Vesuvius) play an important part in the investigations of Bacteria. + +**MOVEMENT.** Many Bacteria are self-motile; the long filaments of *Lactobacillus* exhibit movements resembling those of *Oscillaria*. In many motile forms the presence of cilia or flagella has been proved by the use of special methods. In some cases only one or two cilia attached at one end both ends (Fig. 25) are distributed irregularly over the whole body; the cilia are apparently elongations of the mucilaginous covering and not, as in the other Algae of the proto- +plasms. In Spirochaetae the movement is produced by the flexibility of the cell wall. Generally speaking, all motile forms have two kinds of swarm-cells (i.e. rotation round the long axis and movement in irregular paths); but either end has an equal power of proceeding forwards. + +The swimming motion must not be confused with the hopping motion of the very minute particles under the microscope (Brownian movement). + +**VEGETATIVE REPRODUCTION takes place by continued transverse** + +BACTERIUM. +29 + +division; hence the name "Fission-Fungi" or "Fission-Algae," has been applied to the Bacterium. + +Structure. The spores are probably developed in two ways. In the *exodophorus* species (Figs. 28, 29), the spore arises as a new cell inside the mother-cell. The spores are strongly refractile, and are much smaller than the mother-cell, and are similar to the aplanospores of other Algae. In addition to these there are the *arthrophorus* species in which the cells, just as in *Nototus* and other Blue-green Algae, assume the properties of spores without previously undergoing an endogenous new construction, and are shed by the parent cell in the course of vegetative generations (Fig. 27). The formation of spores very often commences when the vegetative development begins to be restricted. + + +A diagram showing the structure of a bacterium. The main body is divided into several smaller compartments, each containing a nucleus. The nucleus is surrounded by a cell wall. There are also smaller structures within the main body, possibly representing other cells or organelles. + + +Fig. 27.—Leucobacter muscorum: a, a young, natural size; b, cross section of young cell with spores; c, mature spores; d, successive stages of germination. +The spores are formed in the same way as in *Nototus*, but they may be seen on the external side of the mucilage covering. (See magnified fig.) + + +The spores germinate in *Nototus* by the bursting of the external layer of the cell-wall, either by a transverse or longitudinal cleft, but always in the same way, in the same species (Fig. 28, example of transverse cleavage). + +Distribution. Bacteria and their germs capable of development, are found everywhere, in the air (dust), in surface water, and in the superficial layers of the soil. The number varies very much in accordance with the nature of the place, season, etc. They enter together with air and food, into healthy animals and occur always in their alimentary canal. + +29 + +30 BACTERIA. + +Growth and reproduction depend upon the conditions of temperature. There is a certain minimum, optimum and maximum for each species; for instance (in degrees Centigrade)— + + +A diagram showing the stages of bacterial growth. + + +For, bacteria, like all other cells of living, eucaryotic-celled, is a living, mobile, pair of rods ; a similar rod after the effects of the changes in temperature, and the presence of oxygen (aerobe formation); &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; &c) an extensive stage of spore-formation; + + +Fine, non-living globular, +Minim. rods, partly cylindrical +and without spaces, partly +stretched out into long +spires, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal +spaces, with three longitudinal + +Eubacterium rubrum 4 50 60 70 80 90 100 110 120 130 140 150 160 170 180 190 200 210 220 230 240 250 260 270 280 290 300 310 320 330 340 350 360 370 380 390 400 410 420 430 440 450 460 470 480 490 500 + +Bacillus anthracis + +Spirillum cholerae assoiaton + +Bacterium tuberculoate + +The functions of life cease on a slight excess or minimum temperature. Numerous setting in when either these limits is passed. Crenotricha-throds provided with mucilaginous envelopes may, according to Zopf., sustain a tempera- +ture at which the water would boil at once. The exposure to so low a temperature as --11° for a short time. It is not known at what degree cold the death the Bacteria oc- +cur: the greatest degree heat which the vegetative cells can + +BACTERIlla + +31 + +withstand is about the same as that for other vegetative plant- +cells, namely, about 50-60°C. Certain Bacteria, e.g., E. thermo- +philus, grow and thrive vigorously at 70°C. Many species, on the contrary, are able to bear far higher temperatures (in several species up to 80°C) but do not grow at 100°C; those of +Bacillus subtilis, for instance, can withstand for hours tempera- +ture of 100°C in nutrient solution; the spores remain capable of +development after exposure to a dry heat of 122° C). + +The Bacteria are air, if preserved, killed many times when in +the vegetative condition. The spores however, bear a much +longer period of dryness, some even several years. + +OXYGEN. Some species cannot live without a supply of free +oxygen. These include the Bacteria of the genus Bacillus, the +Hansen-thalli, the Chorda-Micrococcus. Other species can thrive +rigorously without supply of free oxygen, and are even checked in +their development by the admission of air (Anaerobes), e.g., the +bacteria of the genus Clostridium (Clostridium perfringens, Clostridium +spoilator). A distinction may be drawn between obligate and +faculative aerobes and obligate and facultative anaerobes. +Several Bacteria, producing fermentation, may grow without the +aid of oxygen when they are living in a solution in which they can +only respire anaerobically. But these bacteria will not grow when +an only supply of oxygen is available. A great number of the pathogenic Bacteria belong to the facultative anaerobes. + +A luminous Bacterium (Bacillus phosphoreus) which in the +presence of a supply of oxygen gives a bluish-white light, has been found in sea-water. Phosphorescent Bacteria have fre- +quently been observed upon decaying fish-sea, as well as on the +feet of fish. They are also found in fermented meat from cold fish +to beef, etc., the latter may be made luminous. + +Organic carbon compounds are indispensable for all Bacteria, +(except, as it appears, for the nitifying organisms), so that they can +only live in solutions containing organic matter or its derivatives. The +supplies of nitrogen, which also they cannot do without, can be ob- +tained equally well from organic compounds as from inorganic +salts, such as salt-potato or ammonia-combustibles. The various "ab- +sorption" processes are therefore very similar. + +While Moulds and Yeast-Fungi grow best in an acid substratum, +the Bacteria, on the other hand, generally thrive best in a neutral or slightly alkaline one. + +32 + +**BACTERIA** + +In *sterilization*, *disinfection*, and *antiseptic*, means are employed by which the Bacteria are killed, or checked in their development, for instance, by heat (ignition, cooking, hot vapours, hot air, etc.), or poisons (acids, corrosive sublimate). The process of preserv- +ing articles from the action of Bacteria is called *sterilization*; it is essentially sealed, aims at destroying the Bacteria, or the spores of those which already may be present in them, and excluding all others. + +As the Bacteria are unable to assimilate carbon from the car- +bonic acid of the air, but must obtain it from the carbon-com- +pounds already in existence in the organic world, they are either +*asphyxieous* or *parasites*. Some are exclusively either the one or the other. Others are intermediate between these two forms, +transitional forms among them, some of which are at ordinary +times asphyxieous, but may, when occasion offers, complete their +development wholly or partly as parasites—facultative parasites: others are parasitic only during a certain stage of their +development as asphyxieous—facultative asphyxieous. + +All chlorophyll-free organisms act in a transforming and dis- +turbing manner on the organic compounds from which they obtain +their nourishment. In this way they produce, each after its kind, compounds of a less degree of +complexity, i.e. they produce fermentation, putrefaction, sometimes +the formation of poisons, and in living beings often disease. + +Those organisms which contain chlorophyll are called *photosynthetic*; +this word, however, is also employed for similar transformations in purely chemical materials (inorganic ferments or enzymes). + +Many organic ("living") ferments, among which are Yeast- +cells and Bacteria, can be decomposed into certain +inorganic and soluble ferments (enzymes) which may produce +other transformations without themselves being changed. Dif- +ferent organisms may produce in the same substratum different kinds of transformation. For example, the same substance may be produced by different species of Fungi; but in different pro- +portions, and the same species produces in different substrata, +different transformations (e.g. the Vinegar-bacteria oxidize diluted alcohol to vinegar, and eventually to carbonic acid and water). + +In the study of Bacteria it is absolutely necessary to sterilize the vessels employed. This is done by boiling with steam for 10 minutes; then from Bacteria germi and also to preserve the culture from the intrusion of any +foreign germs ("pure-cultures"). A firm, transparent, nutritive medium is + +BACTERIA. +33 + +frequently employed. This may be prepared by adding to the nutrient solu- +tions (broth) either gelatin or, when the Bacteria are to be cultivated at +blood-heat—serum of sheep's or calf's blood, agar-agar or carrageen; serum +of human blood, or any other suitable material. The "nutrient solu- +tures" are frequently employed, Le. the germs are isolated by shaking them +with the method liquid nutrient solution, which is then spread on a glass plate +and allowed to dry. When the plates are examined after 24 hours, large +colonies, these remain separate in the solid substratum and it is easy to puruse +further development. Similar plate cultures may also be cultivated in +the same manner with the addition of a little yeast extract. These can be +placed in "moist chambers" free from Bacteria. By noting a few cells (if pos- +sible) by means of a fine platinum wire, pure cultures for further investi- +gation may be obtained. + +In order to prove the relationship between pathogenic Bacteria and certain +classes of the experimental protozoa, it is necessary to know how the inoculation +of Bacteria into cultures leads into healthy animals, it is very impor- +tant to know this. + +It has not so far been possible to establish a classification of the Bacteria, +as the life-history of many species has not yet been sufficiently investigated. The opinions of botanists are at +variance with each other with regard to the forms of growth of a +particular kind. Some species are pleomorphic (many-formed) +while others possess only one form. + +The following Bacteria are Saprophytes: + +Colonial forms, such as those of water and running water which is impregnated with organic matter; the cell-chains have false branching. According to Zopf, Leciderea oxylus is one of +the forms of this substance, in which, containing ferrous iron +(eg. as FeCO₃), regularly embeds ferrous iron in its sheath by means of +Leciderea oxylus. According to Zopf, the other iron-bacteria, according to Wimogersky (1888), do not continue their growth in water free from protoxide of iron; while they multiply enormously in water which contains this salt of iron. +The forms of development of Chondrocladium dichotomum, lags, +and lakes, are probably due to the activity of the Iron-bacteria. +These forms which, according to Zopf's views, represent the +forms of development of Chondrocladium dichotomum are placed together in fig. 105. In this figure a group of cells is shown at 10 times magnified, attached to a Vachneria. The largest one is branched like a tree, with branches of ordinary form; a specimen with +spirally twisted branches is seen to the right of the figure; at +the left hand side is seen Leciderea oxylus-like form. D shows the + +On the classification of Bacteria see "System der Bakterien," by Dr. +W. Mignola. Jena, 1897. + +W. B. +D + +34 + +BACTERIA. + +manner of branching and an incipient Coccos-formation. C a Coccos-mass whose exit from the sheath has been observed. D the + + +A: A cluster of short rods. +B: A cluster of long, thin rods. +C: A cluster of short, thick rods. +D: A cluster of long, thin rods. +E: A cluster of short, thick rods. +F: A cluster of short, thick rods. +G: A cluster of short, thick rods. +H: A cluster of short, thick rods. +I: A cluster of short, thick rods. +J: A cluster of short, thick rods. +K: A cluster of short, thick rods. +L: A cluster of short, thick rods. +M: A cluster of short, thick rods. +N: A cluster of short, thick rods. +O: A cluster of short, thick rods. +P: A cluster of short, thick rods. +Q: A cluster of short, thick rods. +R: A cluster of short, thick rods. +S: A cluster of short, thick rods. +T: A cluster of short, thick rods. +U: A cluster of short, thick rods. +V: A cluster of short, thick rods. +W: A cluster of short, thick rods. +X: A cluster of short, thick rods. +Y: A cluster of short, thick rods. +Z: A cluster of short, thick rods. +AA: A cluster of short, thick rods. +AB: A cluster of short, thick rods. +AC: A cluster of short, thick rods. +AD: A cluster of short, thick rods. +AE: A cluster of short, thick rods. +AF: A cluster of short, thick rods. +AG: A cluster of short, thick rods. +AH: A cluster of short, thick rods. +AI: A cluster of short, thick rods. +AJ: A cluster of short, thick rods. +AK: A cluster of short, thick rods. +AL: A cluster of short, thick rods. +AM: A cluster of short, thick rods. +AN: A cluster of short, thick rods. +AO: A cluster of short, thick rods. +AP: A cluster of short, thick rods. +AQ: A cluster of short, thick rods. +AR: A cluster of short, thick rods. +AS: A cluster of short, thick rods. +AT: A cluster of short, thick rods. +AU: A cluster of short, thick rods. +AV: A cluster of short, thick rods. +AW: A cluster of short, thick rods. +AX: A cluster of short, thick rods. +AY: A cluster of short, thick rods. +AZ: A cluster of short, thick rods. +BA: A cluster of short, thick rods. +BB: A cluster of short, thick rods. +BC: A cluster of short, thick rods. +BD: A cluster of short, thick rods. +BE: A cluster of short, thick rods. +BF: A cluster of short, thick rods. +BG: A cluster of short, thick rods. +BH: A cluster of short, thick rods. +BI: A cluster of short, thick rods. +BJ: A cluster of short, thick rods. +BK: A cluster of short, thick rods. +BL: A cluster of short, thick rods. +BM: A cluster of short, thick rods. +BN: A cluster of short, thick rods. +BO: A cluster of short, thick rods. +BP: A cluster of short, thick rods. + +SACCHARILL 35 + +and after treatment with picro acid, which causes the chain-like structure to become apparent. G. A portion of a plant with con- +spicuous sheath, two lateral branches are forming before. H. Part of a plant, whose cells have divided and form Cocci. The original +form of the cells in which the Cocci are embedded may still be recognized in the sheath, but they are now enclosed in a con- +spicuous sheath, from which a series of rods is about to emerge; the rod +near the bottom is dead, and has remained lying in the sheath. K part of a plant which is forming Cocci, those at the top are in +the zoogloea-stage, at the base they are elongating to form rods +and Cocci. L. A portion of a plant with several short spirochaetes, +which divide into motile Bacillus-forms; the ruyas at the free +ends indicate the currents which the filaments produce in the water. +M. A spirally-twisted, warming filament, before and after division +of its nucleus. N. A portion of a plant with several short +rods—all of these spirilla, zoogloea, etc., which Zepte has con- +sidered with Ciala diathecia, are according to Winiagrodsky, inde- +pendent organisms. + +Micrococcus acidophilus produces arinal fermentation (transformation of arinal matter into ammoniacal carbonate); sericin; round cells +which unite to form bent chains or a zoogloea.—Several other +kinds of Bacteria have the same action as this one: in damp +soil, on the surface of milk, and on articles of food, acids are pro- +duced by M. nitricusf and several different kinds of Bacteria. + +Micrococcus prodigiosus is found on articles of food containing +starch; "bleeding bread" is caused by this bacterium, which has the power of producing a red pigment; it also occurs in milk, and produces lactic acid. + +Lemonosotus mesentericus is the frog-spawn Bacterium (Fig. 27) +which is found in sugar manufactories, and has the power of +producing acids from sugar. In some of the solutions which have been derived from plants, e.g. in beetroot-solutions in manu- +factories, where large accumulations of musilage are formed at the expense of the sugar, with an evolution of carbonic acid. The +cells are long and thin, and contain many vacuoles; they form thick +musilingae-cell walls, and form white "Nostoc"-clumps. The +musilage eventually deliquesces and the cells separate from each other; +anthorophores—Similar viscous deteriorations occur in +beetroot-wine—may then be drawn out into long, string- +like filaments—ruptures + +Bacterium aceti, the Vinegar-bacterium, oxidizes alcohol into + +36 BACTERIA + +acetic acid (acetum-fermentation) and forms a greyish covering of Bacteria (= Vinegar-mother,) on the surface of the liquid; the acetic acid formed, becomes by continued oxidation by E. acet., again transformed into carbonic acid and water. Aerobic; short cylindrical cells, often united into chains, or to form a zoogloea-like mass, or sometimes into long rods, or long bacilli, or other kinds with ball- or rod-forms sometimes become swollen, spinelike-shape, or oval links; they are supposed to be diseased forms? ("Inversion-forms"). + +Bacillus subtilis (Bacillus lactici, Zopf.) is always found in milk which has stood some time for, and in sour foods (cabbage, cucumbers, etc.); it turns the milk sour by producing lactic acid fermentation in the sugar contained in the milk; the lactic acid formed, is very similar to that produced by Lactobacillus. It resembles the Vinegar-bacteria, occurring as small cylindrical cells, rarely in short rows; not self-motile—Several other Bacteria appear to act in the same way, some occurring in the mouth of animals being; but these are not so numerous as those of the lactic flora. + +The kefir-grains which are added to milk for the preparation of kefir, contain in large numbers a Bacterium (Diplococcus casei) in the zoogloea-form, a Yeast-form, and Racibora lactica. Kefir is a somewhat similar beverage manufactured by the inhabitants of the Caucasus, from the milk of cows, goats, or sheep, and is sometimes used as a medicine. In the production of kefir, lactic acid fermentation takes place first; this is followed by alcoholic fermentation; the alcoholic fermentation in another part, and the casein which had become curdled is partially liquefied (peptised) by an enzyme of a Zoogloea-bacterium. + +Racibora lactica (Racibora bursa), the Butyric acid-bacterium (Fig. 29), is a very common anaerobe which produces fermentation in sugar and lactic-acid salts, and whose principal product is lactic acid. It destroys articles of food and (together with other bacteria) causes putrefaction; its action is essential which is necessary in the making of cheese; it is very active wherever portions of plants are decaying, destroying the cellu- +lose in the cell-walls of herbaceous plants, and is thus useful in the preparation of manure. It is usually short cylindrical, sometimes united into short rows; endo- +3 According to Hansen these are not disease forms, but occur regularly under certain conditions, e.g. temperature. + +**BACTERIA** + +37 + +sporons; the spore-forming cells oval, assume very different forms, and show granulose reaction. The germ-tube grows out in the direction of the long axis of the spore. + +*Bacillus subtilis*, the Hay-bacillus, is developed in all decoccions of hay; a very similar species, *Bacillus ferricillinus*, endosporous (xiphosporous) the spore-wall ruptures transversely on germination. + +*Crenothrix kühniana* occurs in the springs of many baths, in water, in wells or draining-pits. + +*Fungi* are found in the water of the Blue-green Alga *Oscillatoria*. Long filaments formed of cylindrical cells which are attached by one of the ends, but which are nearly always free when observed. The filaments, like those of *Oscillatoria*, describe conical figures in their course, and are often seen to be divided into two branches, one another; sometimes they are wanting; strongly refractive sulphur bulbs are found in the interior. The Beggiatrae are the most prominent of these organisms; they occur very commonly in large numbers, wherever plant or animal remains are de- +caying in water in which sulphurised hydrogen is present; thus for example, *B. alfa* (Fig. 51) is frequently as a white covering or almy film on mud containing organic remains. *B. microlis* is remarkable for its size and its strong peristalsis movements. It is a very active organism, the sulphured hydrogen, and accumu- +late sulphur in the shape of small grains of soft sulphuretted sulphur, which in the living state are dissolved in the crystalline state. They next oxidise this sulphur into sulphuric acid, which is immediately rendered neutral by ab- +sorption of oxygen from the air, +off in the form of a sulphate, thus CaSO₄ is principally changed to CaSO₃. In the absence of sulphur the nutritive processes are suspended, and consequently death occurs either sooner or later. The fluid which only contains traces of organic matter, in which organisms devoid of chlorophyll are not able to exist. The Beggiatrae very frequently form white, bulky masses in sulphur wells and + +Beggiatrae alba: a filament of a blue-green alga. +Pan. 81. - Beggiatrae alba: a filament of a blue-green alga. +The alga is covered with a film of sulphured hydrogen; after some time a con- +siderable amount of sulphured hydrogen has been absorbed; it takes an additional four hours to assimilate this substance; then the alga becomes cyano- +genous, by this means the trans- +portation of oxygen to the vacuoles have become visible. + +38 +BACTERIA. + +in salt water, the traces of organic material which the sulphur water contains proving sufficient for them. The cellulose-fermenta- +tion, to which the sulphur wells are mainly susceptible owe their origin, mainly proceed by the reduction of the organic matter, formed during the cellulose fermentation by the reduction of CaSO₄ is calcium carbonate, and CO₂ by the action of oxygen (Helmholtz, 1871).—Other Sulphur-bacteria, e.g., the purple Sulphur-bacteria, r. e. R. aerogenes, Spirillum sanguineum (Fig. 25), Bacillus sputorum, etc., have their own special mode of nutrition. In these bacteria, which like chlorophyll, has the power, in the presence of light, of giving off oxygen (as proven by T. W. Eigendam, 1888; an oxygen-consuming Bacterium). These three kinds of bacteria are found in water according to Wundtberg, not photomembrane cells but embrace numerous species. + +Many Spirilla (Spirillum tenuis, S. undulata, S. plicillate, and others) are found in decaying liquids. + +Bacteria (especially Bacilli) are the cause of many substances emitting a putrid smell and of various changes in milk. + +Parasitic Bacteria are also found in human beings; but the relation between 'host' and parasite may vary in considerable degree. Some parasites do no injury to their host, others produce dangerous contagious diseases; some choose only a special kind as host, while others attack all kinds of hosts indiscriminately. There are further specific and individual differences with regard to the propagation of the host, and every individual has not the same receptivity at all times. + +The number of human BACTERIA. Several of the above mentioned asphyxieties may also occur in the alimentary canal of human beings; e.g., the Hay-faeculae, the Butyrice-acidifica- +tion, etc., but the gastric juice prevents the development of others, at least even those which are harmful. The "bacillus cere- +trical," packet-bacterium," is only known to occur in the stomach and intestines of human beings, and makes its appearance in cer- +tain diseases of the stomach (dilatation of the stomach, etc.) in great numbers; it is also found in certain cases of enteric fever. It occurs in somewhat cubical masses of roundish cells (Fig. 25). + +Lethal dangerous parasites. In the mouth, especially between and on the teeth, a great many Bacteria are to be found (more than fifty different species have been described); they are chiefly very thin filaments which are united into bundles). Micrococcii in large lumps, Spirochete colána, etc. Some of them are known to be injurious, as they contribute in various ways to the decay of the teeth (necrosis dentium); a Micrococcus, for instance, forms bacterioidal + +EUTHERIA. + +in materials containing sugar and starch, and the acid dissolves the lime salts in the external layers of the teeth; those parts of the tooth thus deprived of lime are attacked by other Bacteria, and become dissolved. Inflammation in the tissues at the root of a tooth, is usually produced by septic materials which have been formed by Bacteria. + +DANGEROUS PARASITES. In a large number of the infectious diseases of human beings and animals, it has been possible to prove that parasitic bacteria are the cause of the disease. Various pathogenic bacteria of this nature, belonging to the Cocci, Rods, and Spinal Bacteria, groups are mentioned in the following: + +Pathogenic Micrococci. *Staphylococcus pyogenes aureus* produces a disease of various names, but with a severe presence in (internal organs). Some effects are produced by: +*Streptococcus pyogenes*, which is the most frequent cause of malignant purulent fever; it is perhaps identical with— +*Streptococcus haemolyticus*, which is the cause of erysipelas in human beings. +*Diplococcus pneumoniae (A. Fränkel) is the cause of pneumonia, and of the epidemic cerebro-spinal meningitis.* +*Gonococcus (Neisser) is the cause of gonorrhoea and inflammation of the urethra.* + +Pathogenic Rod-Bacteria. *Bacillus cholerae gallinarum*, an aerobic, facultative parasite which produces fowl-cholera among poultry; it is easily cultivated on various substrates as a sapro- phyte, and may also be transmitted through wounds and by food, and may also be communicated to mammals. +*Bacillus anthracis*, the *Bacillus* chalarae (Fig. 32), chiefly attacks mammals, especially herbivorous animals (house mice, guinea-pigs, rabbits, etc.), but also birds (chickens, pigeons, etc.) (including human beings), and in a still less degree the Carnivores. Aerobic. Cylindrical cells, 3-4 times as long as broad, united into long rod-like bodies, which may elongate into long, bent, and somewhat twisted rods. The mode of transmission takes place without the throwing off of any spore-membrane (compare Hay-bacillius p. 37 which resembles it). Contagion may take place both by introduction into wounds, and from the mucous membranes by inhalation or contact with infected material, and by spores; in intestinal anthrax, however, only by spores. The Bacillus multiplicates as soon as it has entered the blood, and the anthrax disease commences. The Bacilli not only give off poison, + +A diagram showing different types of bacteria. + +40 + +**SACCHARIA** + +but also deprive the blood of its oxygen. Vegetative cells only occur in living animals. This species is a *faculative parasite* which in the first stage is a saprophyte, and only in this condition forms spores. + +*Barilla barillenae* produces tuberculosis in human beings, also in domestic animals (pernicious). It is a distinct parasite, but may also live saprophytically. It is rod-formed, often slightly bent, and is recognized principally by its action with dinitro- (when stained with an alkaline solution of methyl-blue or carbol-fuchs). + +A diagram showing the structure of Bacillus barillenae. +Fig. 32.—*Bacillus barillenae*. The formation of the spores, magnified hundreds of times. + +sin, it retains the colour for a long time even in solutions of mineral acids, in contrast with the majority of well-known Bacteria); it probably forms spores which are able to resist heat, dryness, etc. + +*Bacillus luteus* produces leprosy; *Bacillus maltese* produces glanders; *Bacillus tetani*, *bacillus anthracis*, *bacillus cereus*, *bacillus subtilis*, *bacillus diphtheriae*, *diphtheria*; *bacillus typhoides*, typhoid fever, etc. + +**Pathogenic Spiral Bacteria.** *Spirochete obramovi* (Fig. 24) produces intermittent fever (febris recurrenta); it makes its appearance in the blood during the attacks of fever, but it is not to be found during intervals when there is no fever. Obligate parasite. + +*Spirillum cholerai asiaticum* (Microspira comma) without doubt produces Asiatic cholera; an exceedingly motile spirillum, which is also found in short, bent rods (known as the "Comma-bacillus"), + +**EACTERIA.** + +It lives in the intestines of those attacked by the disease, and gives off a strong poison which enters the body. It is easily cultivated as a saprophyte. + +A great many circumstances seem to show that a number of other infections diseases (syphilis, small-pox, scarlet-fever, measles, yellow fever, etc.) are caused by Bacteria, but this has not been proved with certainty in all cases. + +It has been possible by means of special cultivations (ample supply of oxygen, high temperature, antiseptic materials) to produce varieties of Bacteria which differ from each other (e.g., *Bacillus coli* and the anthrax *Bacteria*) physiologically varieties which are distinct from those appearing in nature and possess a less degree of "virulence", i.e. produce fever and less dangerous symptoms in the animal host. The importance of such physiological varieties can come to be of great practical importance from the fact that they are used as vaccines, i.e. these harmless species produce in the animals inoculated with them immunity from the pathogenic infection. Because of this, which they have acquired, they are no longer affected by the change of the products of one or more of the Bacteria, but we do not yet know anything about the way in which they act on the animal + + +A diagram showing two blood-cells labeled "a" and "b". The text below reads: "Fig. 38.--a and b. The same blood-cell of a Frog, a in the act of engulfing an antirrheumatic Bacterium, b in the act of engulfing a few minutes when the bacterium has been shortened." + + +The white blood corpuscles, according to the Metchnikoff, play the part of "Phagocytes" by absorbing and destroying the less virulent Bacteria which have entered the organism. + +40n. +BACTERIA. + +blood, and by so doing they are gradually enabled to overcome those of a more virulent nature. + +**BACTERIA PATHOGENIC TO PLANTS.** Recent investigations have thoroughly proved the parasitization of Bacteria upon plants—trees, grasses, etc., but whether these plants have undoubtedly been immune to these organisms, though their behaviour as vegetable parasites in other cases has not been strictly defined. The following examples may be quoted: + +A cell from Turnip attacked by *Pseudomonas destructans*. The bacteria are seen in the cell-walls, along with the track of the middle lamella. The cell-wall is much thinner than that of the surrounding leaf-sheets along the middle lamella, in which the destruction is more strongly marked. B. *P. destructans* with single polar flagellum. + +*Pseudomonas destructans* causes the White Rot of the Turnip (Brassica napus). The action of this Bacterium upon the cells of its host is similar to that of certain parasitic Fungi; it produces a toxin which dissolves the middle lamella of the plant-cells, a process which has the power of dissolving the middle lamella, and causing the softening and swelling of the cell-wall. By this means the Bacteria rapidly invade the tissues of the host, burrowing through the cell-walls and extending into the cell-contents and intercellular spaces (Fig. 38a); the collapse occurs with the death of the cells, + +A + +b + +B + +CONJUGATE. 41 + +and the root is reduced to a mere watery pulp. This organism generally infests the plant through a wound, but it is able to enter the epidermis of undeveloped leaves. + +*Pseudomonas campestris* produces a brown discolouration of the vascular tissues in the roots and leaves of Cruciferaeous plants. It attacks the woody portion of the vascular bundles, and is found in great numbers blocking up the wood-vessels. The infection of the leaves may take place through the water-pores, and spread thence along the vascular bundles to other parts of the plant. + +*Pseudomonas hyacinthi* is pathogenic to Hyacinths, spreading especially through the vascular system. Yellow spots are found on the bulbs and foliage which are due to the lesions becoming filled with a yellowish pus produced by this organism. + +*Bacillus subtilis* attacks the Tomato, Egg-plant, and Potato, causing the withering and final death of the young shoots. + +*Bacillus betoi* gives rise to the "Gummosis" of the Sugar Beet. + +*Microccus tritici* is an organism which infects the grain of Wheat, and preys upon the proteins and starch, forming what is known as "Pink Wheat." + +*Bacillus malii*, it has lately been shown, is the cause of the blisters so common on the Apple and Pear. This parasite is probably carried by Aphidids, and affects an entrance through the wounds caused by these insects. + +Class 5. Conjugate. + +The Algae belonging to this class have chlorophyll, and pyrenoid round which starch is formed. The cells divide only in one direction, they live solitarily, or united to form filaments which generally float freely (solids attached). Swarm-cells are wanting. +The fertilization is ingamorous (conjugation) and takes place by means of zoospores. The zygote, after a period of rest, produces, immediately on germination, one or more new vegetative + +42 + +CONJUGATE. + +individuals; sometimes akinetes or splanosporae are formed in addition. They only occur in fresh or slightly brackish water. +Order 1. Desmidaceae. The cells generally present markings on the outer wall, and are mostly divided into two symmetrical halves by a transverse wall, which, however, there is no symmetrical division of the protoplasmic cell-contents. The cell-wall consists nearly always of two layers, the one overlapping the other (Fig. 35 C). The cells either live solitary or are united into innumerable filaments. The formation of protospores, formed by the fusion of the two conjugating cells, is a symmetrical division; on germination produces one (or after division 2, 4 or 8) new vegetative individual. The chromatophores are either star-, plate-, or band-shaped, and regularly arranged round the long axis of the cell. + +Fig. 36.—A cell of *Dyssimnium brevistem*, external view showing the distinction of the pores. A A portion of the same cell, showing the pores with surrounding protoplasmic projections. C Cut surface of *Euplectra* *wanseri* during cell-divisions ; the external pores being closed by a transverse wall. D A portion of a cell of *Desmidium* *pulchrum*. + +The Desmidaceae are not able to swim independently; many species, however, show movements of different kinds by rising and sliding forward on the substratum. Those movements, which are partly dependent upon, and partly independent of light and the force of gravitation, are connected with the protrusion of a mesoglea-projection. This mesoglea, which is produced by the whole individual, may acquire a prismatic structure, it is secreted by the protoplasmic threads which project through certain pores definitely situated in the walls (Fig. 35 A–D). + +Narrazione is a genus belonging to this order by division. A good example of this is found in *Cosmarium botrya* (Fig. 36 A–D). The nucleus and chromatophores divide, and simultaneously the central indentation becomes deeper, the outer wall is then ruptured making a short, circular canal between the two halves to which it is attached (Fig. 36 C). After elongation the canal is divided by a central transverse wall, which commences as a ring round its + +CONJUGATE. +43 + +inner surface and gradually forms a complete septum. The dividing wall gradually splits, and the two individuals separate from each other, each having one an old and a new half. The two + +A, B, C, D +Fig. 36.—Coniariaceae botryoides. A-D Different stages of cell-divisio. + +daughter-cells bulge out, receive a supply of contents from the parent-cell, and gradually attain their mature size and development (Fig. 36 f-f-D). Exceptions to this occur in some forms. + +In the Coniariaceae, the cells are often so large that where the two conjugating cells unite by a short tube (conjugation-canals), which is not developed at any particular point. The plasmodiocytes merge together after the dissolution of the dividing wall, like two drops of water, almost without any trace of preceding construction, except that the whole of the outer layer of the cell is in contact with the conjugating cells. The conjugating cells in the others lie either transversely (e.g. Cosmarium, Fig. 37 d ; Staurastrum, etc.), or parallel to one another (e.g. Pentium, Closterium, etc.), and + +Fig. 37.—Coniariaceae monosporic. a-c same individual seen from the side, from the end, and from the edge; d-f stages of conjugation; p-d germination of the zygote. +Fig. 37.—Coniariaceae monosporic. a-c same individual seen from the side, from the end, and from the edge; d-f stages of conjugation; p-d germination of the zygote. + +emit a short conjugation-canal (Fig. 37 d) from the centre of that side of each cell which is turned towards the other one. These canals touch, become spherical, and on the absorption of the divided contents they form a long conjugation-canal (Fig. 37 e), which is often surrounded by a mucilaginous envelope. The zygote, which is often spherical, is surrounded by a thick cell-wall, consisting of three layers; the outermost of these + +44 + +CONJUGATE + +sometimes bears thorn-like projections, which in some species are simple (Fig. 37 f), in others branched or variably marked ; in some, however, it remains always smooth (e.g. *Tetramorus*, *Desmidium*). Deviation from this mode of conjugation may occur within one species, e.g. *Desmidium* *cylindricum*. In the formation of the contents of the zygote emerge, surrounded by the innermost layers of the wall (Fig. 37 g, h), and generally divide into two parts which develop into two new individuals, placed transversely to each other (Fig. 37 i); these may have a somewhat more simple marking than is generally possessed by the species. + +A B C D E F G H I +Fig. 38.—*Desmidium*. A *Glotterus* *quadriform*; B *Fusius* *crassicaulis*; C *Muscus* *crassus* (front and side view); D *Rudisius* *dolosus*; E *Streptocarpus* *medullaris* (cut view). + +The most frequent genera are— + +A. Solitary cells : *Mesophyllum*, *Pezium* (Fig. 38 E), *Ctenobryon*, *Echinodorus*, *Heterostoma*, *Lemna*, *Lemnoides*, *Lemnochara*, *Lemnochara* (Fig. 38 f, g), *Xanthidium*, *Streptocarpus* (Fig. 38 E), *Platymenium*, *Dichotomum*, *Pterocarpon*, B. Cells in pairs : *Zygnema*, *Zygnemopsis*, *Zygnematale*, *Zygnematales*, *Gymnostoma*, *Anclodiscus*, *Gymnosporus*. + +Order 2. Zygnemacaea. Cell-wall without markings. The cells are cylindrical, not constricted in the centre, and (generally) united into simple, unbranched filaments. The whole contents of the conjugating cells take part in the formation of the zygote, which on division gives rise to two new individuals. + +*Spirogyra* is easily recognised by its spiral chlorophyll band ; Zygnema has two star-like chromatophores in each cell (Fig. 40); both these genera are very common Algae in ponds and ditches. + +CONJUGATE. +45 + +The conjugation among the Zygnemaceae takes place in the following manner: the cells of two filaments, lying side by side, or + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +A + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +B + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +C + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +D + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +E + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +F + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +G + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +H + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +I + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +J + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +K + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +L + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +M + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +N + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +O + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +P + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +Q + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +R + +A diagram showing the process of conjugation in Zygnemataceae. The two cells, one being situated above the other in the same filament (Fig. 41), push out small protuberances opposite each other (Fig. 39, a, b, c); these finally meet, and the dividing wall is absorbed so that a tube is formed connecting one cell with the other. +S + +A diagram showing three stages of conjugation between two zoospores of Spirogyra vulgaris: In stage Ia both zoospores are still alive; they glide through their respective confluences until they come into contact at some point on their periphery; then they round off to form an intercellular space which becomes filled up by cytoplasmic contents; this space remains open during all subsequent stages; when both zoospores have rounded off they become connected by means of an intercellular bridge which grows from their peripheries towards their center; this bridge grows until it fills up completely both spaces between them; then both zoospores round off again to form new zoospores which are now free from their parent body; this stage corresponds to stage Ib; stage II shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage IIb; stage III shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage IIIb; stage IV shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage IVb; stage V shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage Vb; stage VI shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage VIb; stage VII shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage VIIb; stage VIII shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage VIIIb; stage IX shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage IXb; stage X shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage Xb; stage XI shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage XIb; stage XII shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage XIIb; stage XIII shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage XIIIb; stage XIV shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage XIVb; stage XV shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage XVb; stage XVI shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage XVIb; stage XVII shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage XVIIb; stage XVIII shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage XVIIIb; stage XIX shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage XIXb; stage XX shows how both zoospores have rounded off again to form new zoospores which are now free from their parent body; this stage corresponds to stage XXb; + +**CONJUGATE** + +At first glance it may appear as though conjugation occurs only between two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arranged filaments. + +**Zygnema** *sp.* has been observed by me undergoing conjugation under conditions similar to those described for *Spirogyra* *vulgaris*. It was found that after having passed through several stages of division and growth it became possible for two filaments lying side by side or parallelly arrangedfilament + +46 + +**Chlorophyceae.** + +may be found between the cells in the two filaments, those in the one whose protoplasmic contents pass over being cylindrical, while those of the recipient one are more barrel-shaped, and of a larger diameter. The former may be regarded as a male, the latter as a female plant. The zygote germinates after a period of rest, and grows up to form a new plant. + +Order 3. **Mesocarpaceae.** The cell-walls are globular, uncon- +stricted in the centre, and united into simple unbranched filaments. +The chromatophore consists of an axial chlorophyll-plate, with several smaller ones on each side, and containing a nucleus of two cells (Fig. 45) (sometimes three or four), but the whole pro- +toplasmic contents of the cells do not take part in this process, a +portion always remaining behind; the anlagenomes coalesce in +the conjugation-cell. The zygote then forms appears incapable +of germination until after 2-3 divisions. Of the cells so formed, + +Fig. 45.—Mesocarpaceae. Cells showing various modes of conjugation; at $a$ tris- +mion ; $b$ quadruplication ; $c$ quadruplication of the zygote. + +**Class 6. Chlorophyceae (Green Algae).** + +Those Algae are coloured green by chlorophyll, seldom in com- +bination with other colouring matter, and then especially with red. +The product of sexual reproduction is a zygote which generally +accumulates round certain specially formed portions of protoplasm +termed pyrenoids. The thallus is unicellular or multi-celled; in the +higher forms it is often divided into stem and leaf. The sexual reproduction takes place in various ways; the sexual reproduction is effected by con- +jugation of motile gametes, or by oogamous fertilization. The + +PROTOCOCCIDAE: 47 + +warm-cells (zoospores, gametes, and spermatocysts) are con- +structed symmetrical, and have three protophagous cilia, these +generally being attached to the front end of the warm-cell. +Most of these Algae live in water (fresh or salt); some are found +upon damp soil, stones, or tree-stems, and some live enclosed in +other organisms. + +The Class is divided into three families: + +1. **Protoocoecidae**: Volvoxaceae, Tetrasporaceae, Chloro- +sphaeraceae, Phaeococcaceae, Protococcaceae, Hydrodytracaceae, +Myriococcaceae, Ulvaceae, Ulvulaceae, Chlorellaaceae, Myriococcaceae, +Cylindrocarpales, Chlorophyceae, Chlorophytae, Chlorophytae, +Cladophoraceae, Gomontiaceae, Sphondyliaceae. + +3. **Siphonale**: Berytidiacae, Bryopodiacae, Berbisciae, Vau- +cheriaceae, Phyllospiroaceae, Caulopercae, Codinaeae, Valoniaeae, +Dactylococcaceae. + +Family 1. Protocoecidae + +The Algae which belong to this group are uni- or multi-cellular +with the cells more or less firmly connected, sometimes in a definite, +sometimes in an indefinite form (Fig. 47). Colonies are formed either by division of the individual cells or by the union of two or more individuals. +The cell is usually spherical or ellipsoidal; the colony may be in this latter way termed a thallus. Apical cells and branching are absent. Multiplication by division; sexual reproduction by zoo- +spores rarely by zoogamia. Sexual reproduction may be wanting, or it takes place in a monogenously rarely by zoogamia manner. + +Some are attached by means of a stalk to other objects (Chara- +ciae; Fig. 49), others occur as "Endophytes" in the tissues of certain Mosses or Fennoscopes, e.g., Chlorodictyonum; some in Lemna +(Trichoceros), Utricularia (Utriculina), Monostroma (Monostromata), +and Peplispora; *Phylogymnium* in the leaves of *Lemna* nut- +matoria; *Ajaea*, *Chlora*, and species of Grasses; *Sciolinophaera* +in the leaves of *Hypnum* and *Lemna trinervia*; the remainder +were formerly considered to belong to this family have been proved to be higher Algae in stages of development. + +Of the 10 genera mentioned in this order are either +uni- or multi-cellular; and during the essential part of their life +are free-swimming organisms. They are generally encased in a +mucilaginous envelope, through which 2-6 cilia project from every w.a + +48 +PROTOCOCCODES. + +cell. The vegetative reproduction takes place by the division of all, or few, of the cells of the individual; in some a palmitic-stage is found in addition. The sexual reproduction takes place by isogamous or oogamous fertilisation. + +The Volvoxaceae may be considered to include the original forms of the Chlorophyceae, because, among other reasons, the motile stage is here the most promi- +nent; thus the Volvox, which is a motile cell, is the only form intermediate to the Saprosporeae may perhaps be found amongst them. +Three series of green Algae may be supposed to have taken their origin from the Volvoxaceae. The first series consists of the Chlamydomonads, whose conjugation is the nearest to the fertilisation in Chlorophyceae's palmita; +the Pirococcocoeae in which the vegetative divisions have disappeared, +while the sexual reproduction takes place through short spores— +and Tetracarpaceae, in which the vegetative divisions are more prominent, +whilst the swarming stage is less so. + +A. UNICELLULAR INDIVIDUALS. The principle genera are : Chla- +mymodons, Spheroella, Phacotus.—Spheroella nivalis is the Alga +which produces the phenomenon of " Snow," well known on +high mountains and in ice and snow fields during winter months. +The red colouring matter which appears in this and other green +Algae, especially in the resting cells, is produced by the alternation +of chlorophyll with carotinoides. + +Phacotus nivalis has an outer covering incrusted with lime, +which, at death, or after division, opens out into two halves. +Species may be found among Chlamydomonads, in which conjuga- +tion takes place between gametes of similar size without cell-wall, +or between gametes of different sizes. In some cases conjugation +takes place between male and female splanagomates which are +surrounded by a mucilaginous envelope. + +B. MULTICELLULAR INDIVIDUALS. +The most important genera are Goniom, Stephanoicobrea, Pandor- +inae. The Goniom has 3 or 5 cells arranged in a definite pattern in a flat plate (Fig. 44). Pandorina (Fig. 45), +has 16 cells arranged in a sphere (Fig. 45). +The sexual reproduction takes place in this way each cell, after having +rounded off, and after the withdrawal of the cilia, divides itself + +Fig. 45.—Goniom pandorina. + +PROTOCOCCOIDES. +49 + +into 16 new ones (Fig. 45 B), each forming a new individual, +which soon grows to the size of the mother-individual. It was +in this Alga that the conjugation of self-motile gametes was +first discovered by Pringsheim, 1860. When conjugation is +about to take place, each cell divides into sixteen, as in vegeta- +tive reproduction, but the 16 x 16 cells do not separate from one +another (Fig. 45 C, female gametes, and D, male gametes), and + + +A: A large cell with several smaller cells around it. +B: A group of smaller cells. +C: A cluster of small cells. +D: A cluster of small cells. +E: A cluster of small cells. +F: A cluster of small cells. +G: A cluster of small cells. +H: A cluster of small cells. +I: A cluster of small cells. +J: A cluster of small cells. +K: A cluster of small cells. +L: A cluster of small cells. +M: A cluster of small cells. +N: A cluster of small cells. +O: A cluster of small cells. +P: A cluster of small cells. +Q: A cluster of small cells. +R: A cluster of small cells. +S: A cluster of small cells. +T: A cluster of small cells. +U: A cluster of small cells. +V: A cluster of small cells. +W: A cluster of small cells. +X: A cluster of small cells. +Y: A cluster of small cells. +Z: A cluster of small cells. +AA: A cluster of small cells. +AB: A cluster of small cells. +AC: A cluster of small cells. +AD: A cluster of small cells. +AE: A cluster of small cells. +AF: A cluster of small cells. +AG: A cluster of small cells. +AH: A cluster of small cells. +AI: A cluster of small cells. +AJ: A cluster of small cells. +AK: A cluster of small cells. +AL: A cluster of small cells. +AM: A cluster of small cells. +AN: A cluster of small cells. +AO: A cluster of small cells. +AP: A cluster of small cells. +AQ: A cluster of small cells. +AR: A cluster of small cells. +AS: A cluster of small cells. +AT: A cluster of small cells. +AU: A cluster of small cells. +AV: A cluster of small cells. +AW: A cluster of small cells. +AX: A cluster of small cells. +AY: A cluster of small cells. +AZ: A cluster of small cells. +BA: A cluster of small cells. +BB: A cluster of small cells. +BC: A cluster of small cells. +BD: A cluster of small cells. +BE: A cluster of small cells. +BF: A cluster of small cells. +BG: A cluster of small cells. +BH: A cluster of small cells. +BI: A cluster of small cells. +BJ: A cluster of small cells. +BK: A cluster of small cells. +BL: A cluster of small cells. +BM: A cluster of small cells. +BN: A cluster of small cells. +BO: A cluster of small cells. +BP: A cluster of small cells. +BQ: A cluster of small cells. +BR: A cluster of small cells. +BS: A cluster of small cells. +BT: A cluster of small cells. +BU: A cluster of small cells. + +50 +PHOTOCOCCIDAE. + +has at first a large colourless anterior end, 4 cilia, and 2 "eye- +spores" (Fig. 45 G), but these soon disappear and the cell becomes +uniformly dark-green and spherical, and surrounds itself with a +thick cell-wall, losing at the same time its power of motion: the +zygote (Fig. 45 H) is formed, and becomes later on a deep red +colour. The zygote divides into two daughter cells, whose +contents burst open the wall (Fig. 45 J), and emerge as a large +swarmspore (Fig. 45 K) which divides into 16 cells, and the first +small individual is formed (Fig. 45 L, M). + +*Endocystis* is like *Pandorina* in structure, but stands somewhat + +**Fig. 45.** *Folus globus*, sexual individuals ; *a* zoosporic which have formed spermato- +sides ; *b* oogonium. + +higher, since the contract between the conjugating sexual cells is +greater, the female one being a motile zoospore. + +The habit of this species is shown in Fig. 46. + +The cells are here arranged on the circumference of a sphere, and +enclose a cavity filled with mucilage. The number of these cells +may vary from 300-2500, of which the majority are vegetative +and not nutritive, but some may lay down large masses of mucilage +(Fig. 46 b); others, which may appear as solitary individuals, +divide and form disc-shaped masses of from 8-256 small spermato- + +PROTOCOCCACEAE. 51 + +zooids (Fig. 46 c). After the zoosphere has been fertilized by these, the zoosphere surrounds itself by a thick, sometimes thorny cell-wall, and on germination becomes a new individual of few cells. +A few cells conspicuous by their larger size may be found (1-8, but generally 8) in certain individuals, and these provide the vegeta- +tive division of the colony. The zoosphere is usually sessile. + +Order 3. Tetraprotococcaceae. These reproduce both by vegetative divisions and swarmsomes, some have also gamete-conjugation. The principal genera are: +Tetraporus, Aplastodiscus, Dictyochlorella, Dictyopharum, Chloromagnus, +Chlorococcus, Chlorocystis. + +Order 4. Pterococcaceae. In this order the swarming stages and sexual reproduction are entirely absent. Vegetative repro- +duction by division. The principal genera are: Pterococcus (Fig. +47), Sphaeromonas (Fig. 48), Raphidium, Oxyceps, Schizochytrium, +Corynothrix, Chlamydosporium. Pterococcus is one of the most common Algae throughout the world, occurring as green +coverings on tree-stems, and damp walls, and it is one of the most +common lichen-gondia. + +![Fig. 47.—Pterococcus subulatus.](image) + +Order 5. Protococcaceae. The cells are motionless, free or +affixed on a stalk (e.g. Characium, Fig. 40), either separate or +loosely bound to one another; they never form multicellular +individuals. Multiplication by division is very rare. Reproduction takes +place by swarmsomes, which have 1 or 2 cells, +and sexual reproduction in some by gamete- +conjugation. The principal genera are: Chlo- +rosporella, Chlorocystis, Chlorophyllum, Scuticaria, +Ophiogymnion, Scuticium. + +Order 6. Hydrodictyaceae. The indi- +viduals are unicellular and remain until after +the zoospore-stage is definitely formed; +families (comodo). Ordinary vegetative division is wanting, but + +![Fig. 48.—Raphidium subulatum](image) + +51 + +52 +PHOTOGONODEM. + +asexual reproduction takes place by zoospores (or by motoneless cells without cilia), which unite and form a family similar to the mother-family, inside the mother-cell in a multinucleated envelope. Where sexual reproduction is found it takes place by gamete-conjugation. The principal genera are : Podiatræum (Fig. 30), Caudatærum, Hydrodromus (Fig. 31). + +The genus Podiatræum, Hydrodromus, *Heterotricha* *solatium* (Water-net) is formed of a large number of cells which are cylindrical, and attached to one another by the ends (Fig. 51). The asexual reproduction takes place by zoospores, which are formed in large numbers, and which swim about for a time, and then come to rest and arrange themselves into a new net (Fig. 51 a) which is set free by the dissolution of the wall of the mother-cell, grows, and becomes a new cell. + +Fig. 31. - Podiatræum *superbum.* + +**Fig. 31. - Zoospores conjugation.** + +A. A zoospore of *Podiatræum* *superbum*. B. A zoospore of *Hydrodromus* *solatium*. C. A zoospore of *Heterotricha* *solatium*. D. A zoospore of *Heterotricha* *solatium*. E. A zoospore of *Heterotricha* *solatium*. F. A zoospore of *Heterotricha* *solatium*. G. A zoospore of *Heterotricha* *solatium*. H. A zoospore of *Heterotricha* *solatium*. I. A zoospore of *Heterotricha* *solatium*. J. A zoospore of *Heterotricha* *solatium*. K. A zoospore of *Heterotricha* *solatium*. L. A zoospore of *Heterotricha* *solatium*. M. A zoospore of *Heterotricha* *solatium*. N. A zoospore of *Heterotricha* *solatium*. O. A zoospore of *Heterotricha* *solatium*. P. A zoospore of *Heterotricha* *solatium*. Q. A zoospore of *Heterotricha* *solatium*. R. A zoospore of *Heterotricha* *solatium*. S. A zoospore of *Heterotricha* *solatium*. T. A zoospore of *Heterotricha* *solatium*. U. A zoospore of *Heterotricha* *solatium*. V. A zoospore of *Heterotricha* *solatium*. W. A zoospore of *Heterotricha* *solatium*. X. A zoospore of *Heterotricha* *solatium*. Y. A zoospore of *Heterotricha* *solatium*. Z. A zoospore of *Heterotricha* *solatium*. AA. A zoospore of *Heterotricha* *solatium*. BB. A zoospore of *Heterotricha* *solatium*. CC. A zoospore of *Heterotricha* *solatium*. DD. A zoospore of *Heterotricha* *solatium*. EE. A zoospore of *Heterotricha* *solatium*. FF. A zoospore of *Heterotricha* *solatium*. GG. A zoospore of *Heterotricha* *solatium*. HH. A zoospore of *Heterotricha* *solatium*. II. A zoospore of *Heterotricha* *solatium*. JJ. A zoospore of *Heterotricha* *solatium*. KK. A zoospore of *Heterotricha* *solatium*. LL. A zoospore of *Heterotricha* *solatium*. MM. A zoospore of *Heterotricha* *solatium*. NN. A zoospore of *Heterotricha* *solatium*. OO. A zoospore of *Heterotricha* *solatium*. PP. A zoospore of *Heterotricha* *solatium*. QQ. A zoospore of **Podiatræum** **superbum**. + +The sexual reproduction takes place by gamete-conjugation. +The gametes are formed in the same manner as the zoo- +spores, but in larger numbers (30,000-100,000), and swarm out +of the mother-cell (Fig. 51). The sygote forms, on germination, +2-3 large thorny bodies (polyhedra); these swarm about for a time, +and after a period of rest become irregular thorny bodies (polyhedra); +their contents again divide into zoo- +spores, the thorny external coating +of the polyhedra is cast off, +and the exosporae, surrounded by the dilated internal coating, +mute to form a small family, which produces several others in the +manner described. + +Fig. 31. + +**CONFEROIDEA.** + +**53** + +**Family 2. Confervoideæ.** + +The individuals are always multicellular, the cells firmly bound together and united into unbranched or branched filaments, expansions, or masses of cells which grow by intercalary divisions or by the growth of new cells from the base. The filaments are unicellular, but the cells of the remaining three orders contain several nuclei. Asexual reproduction by zoospores, akinetes, or aplanospores. Sexual reproduction by isogamous or oogamous fertilization. + +The Confervoidæ, through the Ulvaceae, are connected with the Tetra- +sporeae, and from the Chlorococcales, which is the most highly developed order of the Ulvaceae, they pass to the Siphonales, which do not take their origin. The Chlorococcales show the nearest approach to the Siphonale. + +Order 1. *Ulvacea*. The thallus consists of one or two layers of parenchymatous cells, connected together to form either a flat membrane (Monostroma, Ulva) or a hollow tube (Enteromorpha), and in some cases a third layer of cells is formed. This section takes place by detached portions of the thallus; or sexually by zoospores or akinetes. Gamete-conjugation is known to take place in some members of this order, the zygote germinating within the resting-stage. The majority are found in salt or brackish water. + +Order 2. *Ullothricacea*. The thallus consists normally of a simple unbranched filament (sometimes a small expansion con- + +A diagram showing a portion of a filament with zoospores. + + +Fig. 31.—*Ulvoidea scandens*, a portion of a filament with zoospores, which are formed two in each cell (zoosporangia); the dark spots are the red "exopores". 1, 2, 3, 6 denote successive stages in the development of the zoospores; b a single zoospore; e an exopore; f an exopore with a zoospore; g an exopore with an exosporangium; h two gametes; i two gametes; j an exopore with an exosporangium; k an exopore with an exosporangium and a gamete; l an exopore with an exosporangium and two gametes; m an exopore with an exosporangium and two gametes; n an exopore with an exosporangium and two gametes; o an exopore with an exosporangium and two gametes; p an exopore with an exosporangium and two gametes; q an exopore with an exosporangium and two gametes; r an exopore with an exosporangium and two gametes; s an exopore with an exosporangium and two gametes; t an exopore with an exosporangium and two gametes; u an exopore with an exosporangium and two gametes; v an exopore with an exosporangium and two gametes; w an exopore with an exosporangium and two gametes; x an exopore with an exosporangium and two gametes; y an exopore with an exosporangium and two gametes; z an exopore with an exosporangium and two gametes. + + +siting of one layer of cells is formed, as in *Sokomorée* and *Prasola* which were formerly described as separate genera). Asexual reproduction takes place by means of zoospores (with + +54 +CONTEINERIDAE. +1, 2, or 4 cilia), akinetes or aphanospores; the last named may germinate immediately, or only after a period of rest. Sexual re- +production takes place by the conjugation of gametes of about the same size, each having two cilia (Fig. 52 d). The zyocyte of Ulothrix, on germination, produces a brood of zoospores which swarm in the water, and then become attached to the substrata (alteration of generations). The gametes may also germinate without conjugation in the same manner as the zoospores. The principal genera are : *Ulothrix*, *Harmadum*, *Conferma*, *Mecu- +spora*. The latter is very rare, and runs fresh water. Nearly all the species of *Conferma* occur in fresh water, stems and stones. + +Order 3. *Chlorophyceae.* The thallus consists of a single, +branching, or creeping filament of cells, often surrounded by mucilage. The cells have only one nucleus. Asexual reproduction by zoospores with 2 or 4 cilia, by akinetes, or aphanospores. In many, conjugation between gametes with 2 cilia may be found. They approximate to the *Characeae* and *Cyanophyceae*. + +The principal genera are : *Stigmacoccus*, *Drapetosilus*, *Chetophora*, *Eutropha*, *Aphanochroa*, *Hypertoxia*, *Phoridium*, *Chlorotrichium*, *Pirichthysia*, *Glycinea*, *Trentepohlia*. Most of the species are greenish in colour, but some are red. A red +colouring material, which occurs in addition to the chlorophyll, they are aerial algae which live on stones (*T. jolitha*, "violin stone," so named on account of its violet-like odour in rainy weather), on rocks ("Pirichthysia verdelis"), or on the rocks ("Pirichthysia verdelis" lives in the Bristish Isles). + +Order 4. *Myxococcales.* The thallus is discoid, consisting of one or more +collaterals, and is always attached. Asexual reproduction by zoospores with 2 +or 4 cilia. Sexual reproduction in some species by the conjugation of gametes +with 8 or 16 cilia (Fig. 53 b). The genus is represented by *Myxococcus* and +*Colochocearhiza*. The species occur in fresh water (*Chelatella*) as well as in salt (*Prismatoceros*), on the surface of the earth (*Dermatocystis* = *Epidermocystis*), and on the leaves of tropical plants, destroying the leaf-nuts (Myrsidea). + +Order 5. *Cylindrocapsaceae.* The thallus consists of a simple +(rarely, in parts, formed of many rows) unbranched filamentous body, covered with a single nucleus, and is enveloped in a thick envelope with a laminated structure. Asexual reproduction by zoospores with 2 cilia, which are formed 1, 2 or 4 in each vegetative cell. The + +55 + +*Confervidae.* + +*Antheridia* are produced by a single cell, or a group of cells, in a filament, dividing several times without increasing in size. Two egg-shaped spermatocysts, each with 2 cells (Fig. 53 D), are formed in each *antheridium*, and escape through an aperture in the side; in the first stages they are enclosed in a bladder-like sac. + +**Fig. 53 B, C.** Other cells of the filament swell out into two segments (Fig. 53 A) which resemble those of *Odlogonium*. After fertilisation the zoospore surrounds itself with a thick wall, and assumes a greenish colour. + +The germination is unknown. The unfertilised zoospores remain green, divide often into 2 daughter-cells, and grow into new filaments. + +This order, which only includes *Oedlogonium*, *Oplodiscus*, forms the connecting link between *Ulothrixis* and *Eudogonium*. The few species (4) occur only in fresh water. + +Order 6. *Edlogoniaceae.* The thallus consists of branched filaments, usually unbranched (*Edlogonium*) filaments, attached in the early stages. The cells may be longer or shorter, and have one nucleus. Asexual reproduction by zoospores, which have a caplet of cilia round the base of the colourless end (Fig. 6 a). *Sexual reproduction* takes place by conjugation, fertilisation. On the division of the zoospore, 2 zoospores are formed (Fig. 54 F). They occur only in fresh or slightly brackish water. The division + +A diagram showing the structure of an antheridium. +B and C show two segments of a filament. +D shows a spermatocyst with two cells. + +56 + +CONVERGENCE. + +of the cells takes place in quite a peculiar and unusual manner. +At the upper end of the cell which is about to divide, a ring-shaped thickening of soft cellulose is formed transversely round the wall; the cell-nucleus of the mother-cell and the protoplasm then divide by a transverse wall into two portions of similar size, and the cell-wall bursts transversely at this line of division, leaving a conical or conical-triangular line of the thickened ring. The cell-wall thus divides into two parts, one short, the "cap," and the lower one much longer, the "stalk." The divisions of the original cell-wall now separate from each other, the cell-nucleus being left in the stalk, and supplying an additional length of cell-wall between the two new cells. This stalk will project a little in front of the piece thus inserted. Thus, between the two new cells is formed near to the uppermost edge of the sheath, and gradually becomes thicker and firmer. + +The inserted piece of wall is called the "cap," and is part of the wall of the upper cell: the remainder is formed by the calf. This mode of division is repeated exactly in the same way, and new caps are formed close below the first one, for every division. + + +A female plant with three reduced ovaries (a) and three ovules (b). The ovule with spermatium (c) soon entering the capsule (d) has just been fertilized by pollen (e), and is developing into a seed (f). B Ovary with three ovules (g), one of which spermatium (h) is emerging. C Portion of flower with three ovules (i), one of which spermatium (j) is emerging. D Portion of flower with three ovules (k), one of which spermatium (l) is emerging. E Portion of flower with three ovules (m), one of which spermatium (n) is emerging. F Portion of flower with three ovules (o), one of which spermatium (p) is emerging. G Portion of flower with three ovules (q), one of which spermatium (r) is emerging. H Portion of flower with three ovules (s), one of which spermatium (t) is emerging. I Portion of flower with three ovules (u), one of which spermatium (v) is emerging. J Portion of flower with three ovules (w), one of which spermatium (x) is emerging. K Portion of flower with three ovules (y), one of which spermatium (z) is emerging. + + +CONFERSVIGIDEA. + +Fortification takes place in the following way. The coenoom is a large ellipsoidal, swollen cell (qg, in Fig. 54 A), whose contents are rounded off into an oosphere with a colourless receptive-spot (see B); an aperture is formed in the wall of the oogonium, through which the spermatzooids are enabled to enter (B). The spermatzooids are then conveyed by the basal cells of the filament, or indirectly. In the latter case a swarm-spore (androgam) is formed which comes to rest, attaches itself + +A small, round, brownish object with a central dark spot. +57 + +Fig. 53.—Cocconate pulvinoida. A A portion of a thallus with organs of reproduction ; B a young sporophyte ; C a mature sporophyte ; D, A, B, m., with energy-irreversible ; E Bipe cocconate, with envelope. Characters of the sporophyte. D Raspone. E spermatocline. + +to an oogonium, germinates, and gives rise to a filament of a very few cells—dicaric-formula (A, B, m.). The spermatzooids are formed by the summit of the antheridium lifting off like a lid. On the germination of the oospore (Q), which takes place in the following spring, 4 zoospores are produced (P), i.e. the sexual generation; these are liberated by the rupture of the envelope of the oospore. + +Order 7. *Coleochetaceae.* The thallus is always attached, and of a disc or cushion-shape, formed by the dichotomous branching of filaments of cells united in a pseudo-parenchy- mal layer. The sexual generation is effected by internal re-production by zoospores with 2 cilia (Fig. 55 D), which may arise in all the cells. Sexual reproduction by coenoom fertilisation. The spermatzooids resemble the swarmspores, but are + +58 + +**COXERYGIDEA.** + +smaller (E), and originate singly (in the species figured) in small conical cells (c. d in A). The oogonia are developed at the extremities of certain branches; they are bottle-shaped cells with very long and thin necks (trichogone), open at the end (a in A); at the base of each oogonium is a spherical oosphere. The spor- +matization takes place by means of a protoplast which passes through an aperture in the wall when the trichogone is absent, and fertilisation having taken place, the oogonium becomes surrounded by a cell-layer (envelope), which grows out from the cells near its base (b in A), and in this way a kind of fruit is formed (B) (sporocarp, *eyerythra*). + +The oospore, next spring, divides and forms a parenchymatous tissue (homologous with the *Mose-spongyphyte*); this bursts open the envelope, and the oospores are liberated, with the spores of the *Mose-capsule* arises in each of the cells, and form a *Colocheite*. We have then, in this case, a still more distinct alternation of generations than in *Oedogonium*. Only one genus, *Colocheites*, is known, but it contains several species, all living in water. + +Order 8. **Cladophoraceae.** This order is probably derived from the *Ulothricaceae*. The thallus consists of a single, un- +branched or branched filament, generally with an apical cell. The cells have each 2 or more nuclei. Sexual reproduction by zoospores is unknown; but there is akinetic formation of gametos with 2 cilia is found in some genera. They occur in salt as well as in fresh water. The principal genera are: *Urospora*, *Chloromorphus*, *Zelkonomus*, *Cladophora*; of the last named genus the oospore is a large, thick-walled body common to salt water; *C. fruticis* and *C. glomerata* in fresh water. + +Order 9. **Goniomonaceae.** *Goniomonas polytricha*, the only species hitherto known, is found on old calcareous shells of certain salt water Molins. + +Order 10. **Sphéroplacaceae.** The thallus consists of free, un- +branched filaments, with very elongated multinucleate cells. Vegetative reproduction by zoospores; sexual reproduction by oogonial fertilisation (see page 13, Fig. 10 D). The oospore has a thick wall (Fig. 10 D) studded with warts, and assumes a colour like that of the parent plant. It germinates in spring, and produces 1-8 zoospores, each with 2 cilia (Fig. 10 E), which grow into new filaments. Only one species, *Sphéroplaca anulosa*, is known. + +A diagram showing the structure of a Cladophora-like organism. + +**Siphonacee.** 39 + +Family 3. Siphonace. + +The thallus has apical growth, and in the vegetative condition consists generally of one single (in the Valoniacae most frequently of more) multinucleate cell which may be much branched, and whose separate parts in the higher forms (e.g. Bryopsis, Fig. 57 ; *Caulerpa*, Fig. 50, etc.) may be differentiated to perform the various physiological functions (as root, stem and leaf). Vegetative reproduction is by means of the zygote (gametous); sexual reproduction by zoospores, akinetes, or aphanopores. Sexual reproduction by gamete-conjugation, rarely by oogamous fertilisation. The zygote or copore germinates as a rule without any resting-stage. + +Most of the Siphonaceae occur in salt water or on damp soil. + +Fig. 58.—*Bryopsis* *glandulosa*. a an entire plant forming *sarcopodium*; b a *sarcopodium*; c an individual with *gametous*; d *z.g.* conjugation; e *z.g.* conjugation; f a *zygote*. + +Many (e.g. *Dugaldiaceae*) are very much increased with lino, and occupy the fossilised condition, in the deposits from the Cretaceous period to the present time. The Siphonaceae are connected by their lowest forms (*Botrydiaceae* or *Valoniae*) with the Protoococcaceae, but show also, through the Valoniacae, points of relationship to the *Chlorophyceae*. + +Order I. Botrydiaceæ. The thallus in the vegetative condition is unicellular, club-shaped, with a small round (*Caulidium*) or repeatedly dichotomously branched system of colourless rhizoids (*flagellum*), by which it is attached to objects immersed in salt water (*Caulidium*); or to short stipes (*Botrydium*). Asexual reproduction by zoospores with one (*Botrydium*) or two + +A diagram showing the structure of a Siphonaceae thallus. + +60 +Siphonaceae. + +cilia, and by aphanospores. The sexual reproduction is only known in *Bryopsis*, and takes place in the following manner: in the part of the thallus which is above ground and in an active vegetative condition, several round cells (Fig. 56 c) are formed, which may be green or red according as they grow under water, or exposed to air. These cells are called "gametangia" and considered as "gametangia" as they produce many gametes (a) provided with two cilia. The zygote (b, c) formed by the conjugaion (e, f, g) may either germinate immediately, or become a thick-walled resting-cell of an irregular angular form. + +Order 3. Bryopodiaceae. The thallus in the vegetative condition is uni- cellular, and consists of a single irregularly branched cell at the lower extremity of branched filaments. A portion of this upper portion is prolonged into a stem-like structure of un- known nature, bearing terminal branches, acrospores, and leaf-like structures. The acrospores are produced in the upper part of the stem, and are separated by a cross- wall from the stem, and become free. The acrospores are of two kinds: one large and one small. Zoospores or any other method of sexual reproduction are unknown. Only one genus, *Bryopsis*, living in salt water. + +Order 4. Derbesiaceae. Only one genus, *Derbesia*, living in salt water. The thallus is a single cell, which has arisen through the coalescence of several, and they resemble the zoospores of *Euglena* by having a circle of cilia attached at the base of its columnar body. + +Order 5. Vaucheriaceae. The thallus consists in the vegetative condition, of a single irregularly or dichotomously branched cell, without differentiation into stem or leaf; root-like organs of attachment may however occur. Asexual reproduction by zoospores, which are formed singly in the extremity of a branch cut off by a transverse wall, containing many nuclei, and bear small cilia situated in pairs, which give the appearance of a fine pile covering the whole or a great part of the surface. Akinides, + +Fan 47.--Bryopsis pinnacea. A, the plant; natural size. +B, a portion (enlarged) which shows the growing point +ofthelower derived from its apical vegetative +extension. +C, colour and smaller. Zoospores or any other method of sexual reproduction are unknown. +Only one genus, Bryopsis, living in salt water. + +Siphonaceae. 61 + +Aplanospores, and phytozomebe (naked masses of protoplasm, without cilia), which creep like an ameba on a substratum) may occur under certain conditions. + +The sexual reproductive organs are formed on short lateral branches and are separated from the vegetative cell (Fig. 65 A) by cell-walls. The spermatocysts, each with two cilia, are developed in the coiled antheridium (A, b). The oogonium is a thick, egg-shaped, often oblique cell, with its protoplasm rounded into a globule. The egg is a hyaline nucleus (A, a) imme- +diately beneath the aperture formed in the wall of the oogonium. A slimy mass, which serves to receive the spermatocysts, is formed in some species in this aperture. The spermatocysts when liberated swim towards and enter the oosphere, which then immedi- +ately surrounds itself with a thick cell-wall. The mature oospore (B) contains a large quantity of oil. At germination the outer cell-wall bursts and a new plant is formed. There is only one known species living in salt as well as in fresh water and on damp soil. + +Order 5. Phyllophoraceae are parasites in the leaves and stalks of flowering plants. + +Order 6. Caulerpaceae. The thallus has distinct differentiation into root, stem, and leaf-like members (Fig. 69) it is unilocular. With the exception of one species branched threads of cell-lime extend from one side to the other serving as stays to support the thallus. Reproduction takes place by detached portions of the thallus; no other modes of reproduction are known. This order may be considered as a primitive form of lichenoid growth. The genus *Caulerpa* consists of more than seventy species which inhabit the tropical seas. + +Order 7. Codiaceae. The thallus has various forms, but with- + +62 +Siphonae. +out distinct differentiation in stem- or leaf-structures, sometimes (e.g. *Halimod*) it is very much increased with time. In the early stages it is multicellular (later, often multilocular), very much branched, with the branches, at any rate partly, so united or grown in amongst one another (Fig. 60) that an apparently purely vegetative reproduction is formed. *Subjects* of *siphonae* are wanting; zoospores (or gametes?) may be developed in some species, however, in special swollen cells, which are similar to that in *Drosera* occurs perhaps in *Coltium*. They are all salt water forms. + +Order 8. Valoniaceae. The thallus is generally multinucleate, without differentiation into stem- or leaf-structures, but the cells are united together and form a leaf-like reticulate expansion (e.g. *Anodymena*). Zoospores are produced by the cells, and they are then formed directly in the vegetative cells. In others (e.g. *Falcaria*) the zoospores, which may be separated through the damaging of a cell, can surround itself with + +A diagram showing a plant structure with multiple branches and cells. +Fig. 60.—*Onodera prolifera* (natural size). + +a cell-wall, and grow into a new plant. No other modes of reproduction are known. The most important genera are: *Falunia*, *Siphonodendron*, *Chamederta*, *Strouma*, *Heterostoma*, and *Anodymena*. + +As already pointed out, the Valoniaceae occupy a somewhat central position among the Siphonae. They are closely related to the *Bryophyta* through *Bryocladon* and the *Bryopteridaceae* through *Falunia*, with the *Dactylotum* through *Chamederta*, and also with the *Cladophoraceae* through *Siphonodendron*, and *Strouma*. + +Siphonae. 63 + +Order 9. *Dasycladaceae.* The thallus consists of an axile longitudinal cell, destitute of transverse walls, attached at the base by root-like organs of attachment, and producing acropetally a short stem, which bears a fertile leaf, and a sterile leaf with limited growth. Axonal reproduction is wanting. Sexual re-production by conjugation of gametes which arise in separate, fertile leaves, either directly or from siphonouspores, which develop into naked gametangia. The principal genera are : *Acotoborula,* *Dasy-cladus,* *Nemocera,* *Cymopedia.* All marine. + +The curiously shaped *Acotoborula mediterranea* (fig. 60) grows on limestone rocks, and shells of mussels in the Mediterranean; it re-sembles a small beehive with a small stem, sometimes as much as nine centimetres in length, and one centimetre in diameter. The cell-membrane is thin, and incrustated with carbonate and oxalate of lime. +Only the lower, roof-like part of the thallus, which penetrates the calcareous substratum survives the winter, and may grow up into a new thallus. The leaves, which grow off the stem, are dichotomyously branched and formed of cylindrical cells separated from each other by cross-walls, but they are not grown together. The fertile leaves are formed by a circle of 70-100 cup-shaped rays (fertile leaves) growing out from the stem. 40-80 siphonospores are formed, which become liberated at the breaking of the shade, and later on are changed to gametangia (compare *Bryo-dawn*) which open by a lid and allow a large number of egg-shaped gametes with two cilia to escape. Gametes from various + +A: A small beehive-like structure with a stem. +B: A magnified view of the beehive-like structure showing its internal structure. + +Fig. 60.—*Acotoborula mediterranea.* Plant (natural size). B Part of a longitudinal section. + +G4 +CHARACEE. +gametangia conjugate with one another; the product of the conju- +gation swarms about for some time, rounds off, and then surrounds +itself with a cell-wall. The zygoth germinates after a period of +rest and then produces a sexual plant. The aplanospores (game- +tangia) thus represent the sexual generation. + +Class 7. Characeae. +The thallus has a stem with nodes and internodes; and whorls +of leaves, on which may be developed the antheridia and oogonia, +are borne at the nodes. Vegetative reproduction by bulbils and +accessory buds, and by spores, are common. The spores are +spherical, and contain a number of flagella in which the spirally +called spermatoida, each with two cilia, are formed. The oogonium is situated terminally, and is first naked, but becomes later +on surrounded by a investment, and forms after fertilisation the +so-called "fruit," the zygote. The zygote develops into a plant by producing a "proembryon," from which the young sexual plant arises as a lateral branch. The Characeae are distinguished by the structure of their vegetative system as well as by the spirally- +coiled sporangia. The Siphonocarpaceae are included in the Order of +Thallophytes, of which, however, the Siphonaceae appear to be their nearest relations. They were formerly, but wrongly, placed near the Mosses. The class contains only one order, the Characeae. + +Order 1. Characeae. Algae with a peculiar colour, often increased with greenish tints, and growing gregariously in large masses at the bottom of fresh and brackish water, and are from a few inches to more than a foot in height. +The stem has long internodes which in *Nidula* are formed of one cylinder enclosing another smaller one; the cells are separated by a cortical layer of smaller ones. The protostem in contact with the cell-wall exhibits in a well-marked degree the movement of rotation (cyctosis), carrying the chlorophyll corpuscles along with it. In *Chara*, the leaves are produced in whorls of small cells (nodal cells) from which the leaves are produced. The leaves are borne in whorls of from 5-12 which regularly alternate with one another as in the higher vertebrate plants; a branch grows out in the axil of the first-formed leaf of each whorl (Fig. 61 A., n.). + +The leaves are constructed in the same manner as the stem; they are divided into a series of joints, but have only a limited + +CHARACEE. 65 + +power of growth; their terminal cell, too, is not enclosed by a cortex. Leaflets are borne at their nodes. The growth of the stem is unlimited, and proceeds by means of an apical cell (Fig. 62 a) which divides into two cells, one lying above the other; the lower one, without + +any further division, becomes one of the long, cylindrical, internodal cells (Fig. 62 a), and the upper one (Fig. 62 a) divides by transverse walls into two segment-cells (Fig. 62 b). These segment-cells divide again by transverse walls into new apical cells. The segment-cell then divides by a transverse wall into two cells, one lying above the other; the lower one, without + + +A Portion of a plant, natural size. +B Portion of a leaf A, with leaflets A-37'; a nucellusiform ; e squamule. +C A shield--Nidula fascia. +D Filaments from antheridia with operculum. +E Free spermatium. + + +Fur. 61.--Chora fragilis. A Portion of a plant, natural size. B Portion of a leaf A, with leaflets A-37'; a nucellusiform ; e squamule. C A shield--Nidula fascia. D Filaments from antheridia with operculum. E Free spermatium. + + + +66 CHARACEE. + +node immediately above it, and those in the lower part of the internode from the node below it. + +The organs of reproduction are very conspicuous by their colour and form. They are always situated on the leaves, the plants being very frequently monopodial (Fig. 61 A, a) or monopodial with the terminal cell of a leaf; they are spherical and become red when mature. Their wall consists of 8 "albida," i.e. of plate-like cells, of which cover the upper half, and are triangular, 4 more are placed at the base. The small part of the antheridium is attached, being quadrilateral, with sides of unequal length. The shields (Fig. 61 C) have dentated edges. + + +A: A small antheridium. +B: A normal antheridium. +C: A shield. +D: A secondary capitate filament. +E: A primary capitate filament. +F: A spermatocyte. +G: A spermatozoon. +H: A nucleus. +I: A transverse wall. +J: A longitudinal wall. +K: A transverse wall. +L: A longitudinal wall. +M: A transverse wall. +N: A longitudinal wall. +O: A transverse wall. +P: A longitudinal wall. +Q: A transverse wall. +R: A longitudinal wall. +S: A transverse wall. +T: A longitudinal wall. +U: A transverse wall. +V: A longitudinal wall. +W: A transverse wall. +X: A longitudinal wall. +Y: A transverse wall. +Z: A longitudinal wall. +AA: A transverse wall. +BB: A longitudinal wall. +CC: A transverse wall. +DD: A longitudinal wall. +EE: A transverse wall. +FF: A longitudinal wall. +GG: A transverse wall. +HH: A longitudinal wall. +II: A transverse wall. +JJ: A longitudinal wall. +KK: A transverse wall. +LL: A longitudinal wall. +MM: A transverse wall. +NN: A longitudinal wall. +OO: A transverse wall. +PP: A longitudinal wall. +QQ: A transverse wall. +RR: A longitudinal wall. +SS: A transverse wall. +TT: A longitudinal wall. +UU: A transverse wall. +VV: A longitudinal wall. +WW: A transverse wall. +XX: A longitudinal wall. +YY: A transverse wall. +ZZ: A longitudinal wall. +AAAAA: Transverse walls in different parts of the antheridium. + + + + +A000000000000000000000000000000000000000000000000000000000000000000000000000000 +B1111111111111111111111111111111111111111111111111111111111111 +C222222222222222222222222222222222222222222222222222 +D33333333333333333333333333333333333333333333 +E4444444444444444444444444444444444444 +F55555555555555555555555555555555555 +G666666666666666666666666666666666 +H7777777777777777777777777777777 +I88888888888888888888888888888 +J9999999999999999999999999999 +K + + + +Fig. 6A.—Chara gracilis; a globular cell, +a, a nodal cell; b, internodal cell; b', its leaves; c, a leaf; d, a leaf stalk; +e, a leaf sheath; f, a leaf sheath stalk; g, a leaf sheath base; h, a leaf sheath base stalk; +i, a leaf sheath base stalk; j, a leaf sheath base stalk; k, a leaf sheath base stalk; +l, a leaf sheath base stalk; m, a leaf sheath base stalk; n, a leaf sheath base stalk; +o, a leaf sheath base stalk; p, a leaf sheath base stalk; q, a leaf sheath base stalk; +r, a leaf sheath base stalk; s, a leaf sheath base stalk; t, a leaf sheath base stalk; +u, a leaf sheath base stalk; v, a leaf sheath base stalk; w, a leaf sheath base stalk; +x, a leaf sheath base stalk; y, a leaf sheath base stalk; z, a leaf sheath base stalk; +aa, aa', aa", aa"', aa"", aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'""aa'\"... + + +Fig. 6B.—Diagram of Chara gracilis: +"cross": a receptive spatule; "spen": a spermatocyte; +"cap": a spermatocyst. + +with the teeth fitting into one another, and their faces ornamented with ridges. From the centre of the internal face of each shield (C) a cylindrical column, the meandrotenes, projects nearly as far as the centre of the antheridium; at the inner end of each of the meandrotenes is placed a long pointed filament (D). From the distal bases six secondary capitates, from each of which four long coiled filaments (D', D') project into the cavity of the antheridium. These filaments are divided by transverse walls into from 10-25 or discoid cells (E), which contain numerous nuclei (F). The nuclei divide and develop (D', D') from the nucleus. The spermatocysts escape from their mother-cell and are set free by the shields separating from one other. + +Page 6 + +CHARACEAE. 67 + +The female organ of reproduction (Fig. 51 D, E) is a small modified shoot, whose apical cell functions as an oogonium. Its protostem forming the coelom which has a colourless receptacle-spot at the summit (Fig. 63 a). The oogonium is situated on a nodal cell, from which 5 cells grow out in a circle and round the oogonium to form a protective investment. These cells divide twice or twice at the top, so that 8 or 10 small cells are cut off, which project above the oogonium and form the so-called "crown" (Fig. 63 k). The crown either drops off or remains attached to the plant to form a central canal for the passage of the spermatozooids. The wall of the oosphere* above the receptive spot becomes thickened, the spermatoid to fuse with the oosphere. + +The oospore, on germination (Fig. 64 p), becomes a small filamentous plant of indefinite growth, with two branches--the proembryo--and from this, as a lateral outgrowth, the sexual generation is produced. + +The order is divided into two sub-orders: + +A. NITELLER. The crown consists of 10 cells; cortex absent; *Nicella*, *Toly- +phus*. + +B. CHARAE. The crown consists of 5 cells; cortex present; *Tolypellia*, *Lam- +pratnuma*, *Zychothamnus*, *Chara*. + +*Chara* is a genus of water plants; in large districts of Europe only female plants are found, yet oospores are formed capable of germination. + +About 40 species of *Chara* are known in the geological formations from the Trias up to the present day. + +68 +Fig. 63.--*Chara* *fuscula*. Germinating oospore (top); 6, 4, p., P, +form sagittate proembryos; 2, 3, p., P, form cylindrical proembryos; at 4 +of the so-called tap-root; at 2 +of the so-called root-like +plant, which appears as a lateral +branch. +Before fertilization the oospore divides and cuts off at the base one or more cells (polar bodies), termed "wendmgrenulum". + +68 +F.EOFOOREE. + +Class 8. *Phaeophyceae* (Olive-Brown Seaweeds). + +The Phaeophyceae are Algae, with chromatophores in which the chlorophyll is masked by a brown colour (*phycochrome*). The pro- +duct of assimilation is a carbohydrate (*fucosan*), acquer true starch. +In the highest forms (*Fucus*) the thallus presents differentiation into stem, leaf, and root-like structures. The sexual reproduction takes place by means of zoospores. This sexual reproduction is effected by the coalescence of motile gametes, or by copulation. +Fertilisation. The sperm-cells are *mononuclear*, each moved by two cilia which are true protoplasmic structures, and generally attached to the egg (fig. 65). The Phaeophyceae are almost entirely salt-water forms, of few species live in fresh water. +The class is divided into two families: +1. *Pheofooree*: 1 Sub-Family, Zoogonic; 2 Sub-Family, Actinice. +2. *Cyclofooree*: Fucaceae. + +Family 1. *Phaeosporae*. + +The family consists of multicellular plants, whose cells are firmly united together to form a thallus; this, in the simplest cases, may be a branched filament of cells (*Ectocarpus*), or, in the highest, may resemble a stem with leaves (*Laminariae*), while all transitional forms may be found between these two. In the thallus there are usually diverse types (e.g. *Ectocarpus*); but by an apical cell (e.g. *Sphaerola*) pseudo-parenchymatous tissue may sometimes be formed by cells, which were originally distinct; in becoming united together. The size of the thallus varies; in some it is microscopic, while in the largest it is many metres in length. + +The vegetative cells in the lower forms are usually unicellular but in those which are more highly developed (*Laminariae* and *Fucus*), they are sometimes so highly differentiated that no conducting systems may be found; the last named systems are formed of long cells with perforated, transverse walls, which bear a strong resemblance to the sieve-tubes in the higher plants. +The colouring matter in the living cells ("phaeophyl") contains + +Fig. 65.—Spermatozoa of *Cystoseira*. + +**PHRAGMOPORELLA** + +69 + +chlorophyll; but this is concealed by a brown ("physophanin"), and a yellow ("physoxanthin") colouring material, and hence all these Algae are a lighter or darker brownish. Starch is not formed. +Asexual reproduction takes place, (1) by zoospores which arise in unicellular zoosporeanaplasia, and are monosymmetric, with a long anterior end (Fig. 65), the longer one being directed forwards and the shorter backwards; or (2) by aplanospores (?). +Sexual reproduction has only been discovered in a few cases, and takes place by means of gametes (oogamous fertilization perhaps occurs in the Tilpideridae). The gametes have the same structure as the zoospores, and arise in multicellular gametangia; these, like the zoospores, may be produced from the zoospores, or arise as modifications from it. The conjugating gametangia may be similar (e.g. *Retocarpus pusillus*), or there may be a more or less pronounced difference of sex, an indication of which is found in *Ectocarpus alceifolius* (Fig. 66). When the gametes in this species have swarmed to a time, some, which are generally larger, + + +A: A plan view of a plant showing its structure. +B: A side view of the same plant. +C: A magnified view of part of the plant. +D: A magnified view of another part of the plant. +E: A magnified view of yet another part of the plant. +F: A magnified view of a different part of the plant. +G: A magnified view of a different part of the plant. +H: A magnified view of a different part of the plant. +I: A magnified view of a different part of the plant. +J: A magnified view of a different part of the plant. +K: A magnified view of a different part of the plant. +L: A magnified view of a different part of the plant. +M: A magnified view of a different part of the plant. +N: A magnified view of a different part of the plant. +O: A magnified view of a different part of the plant. +P: A magnified view of a different part of the plant. +Q: A magnified view of a different part of the plant. +R: A magnified view of a different part of the plant. +S: A magnified view of a different part of the plant. +T: A magnified view of a different part of the plant. +U: A magnified view of a different part of the plant. +V: A magnified view of a different part of the plant. +W: A magnified view of a different part of the plant. +X: A magnified view of a different part of the plant. +Y: A magnified view of a different part of the plant. +Z: A magnified view of a different part of the plant. +AA: A magnified view of a different part of the plant. +BB: A magnified view of a different part of the plant. +CC: A magnified view of a different part of the plant. +DD: A magnified view of a different part of the plant. +EE: A magnified view of a different part of the plant. +FF: A magnified view of a different part of the plant. +GG: A magnified view of a different part of the plant. +HH: A magnified view of a different part of the plant. +II: A magnified view of a different part of the plant. +JJ: A magnified view of a different part of the plant. +KK: A magnified view of a different part of the plant. +LL: A magnified view of a different part of the plant. +MM: A magnified view of a different part of the plant. +NN: A magnified view of a different part of the plant. +OO: A magnified view of a different part of the plant. +PP: A magnified view of a different part of the plant. +QQ: A magnified view of a different part of the plant. +RR: A magnified view of a different part of the plant. +SS: A magnified view of a different part of the plant. +TT: A magnified view of a different part of the plant. +UU: A magnified view of a different part of the plant. +VV: A magnified view of a different part of the plant. +WW: A magnified view of a different part of the plant. +XX: A magnified view of a different part of the plant. +YY: A magnified view of a different part of the plant. +ZZ: A magnified view of a different part of the plant. + +Fig. 66. — *Ectocarpus alceifolius.* I & f. 1. & 2. Two views showing how two plants are joined together at their bases by means +of coming to rest. If 2 is motile, then gametes are surrounded by male +gametangia, and female gametangia are surrounded by female gametangia, +each consisting usually only +of male and female gametes. + +Fig. 67. — *Zonaria colletii.* A Main +gametangium with two male gametangia +(its larger cells). C Female +gametangium. D Main gametangium +with two female gametangia. E Fertilization cell. F Egg. G Conjugating egg. + + + +69 + +70 +**PSEUDOPHORUM** + +are seen to attach themselves by one of the cilia, which by degrees is shortened to form a kind of stalk (compare the spermi-gamete in Fig. 60 II); these are the female gametes, which now become sur-rounded by a number of males endeavouring to conjugate with them, but only one succeeds in effecting fertilisation. The protoplasm of the male gamete is poured into that of the female gamete (x) and a zygote (z) is formed. The male gametes which do not conjugate may germinate, but the plants derived from them are much weaker than those produced by the zygotes. Strongly pronounced sexual differences are observable between the male and female gametes, and female gametes arise in separate gametangia (Fig. 67 A). The male gametes (Fig. 67 D) are much smaller than the female gametes (Fig. 67 O); the latter, after swarming for a short time, withdraw from the parent plant and form zygotes (Fig. +67 B, E), thus we have here a distinct transition to the oogamous fertilisation which is found in the Funaceae. Alteration of genera- +tions is rarely found. + +I. Sub-Family Zoogonicum. + +Reproduction by means of gametes and zoospores. + +Order 1. *Ectocarpus*. The thallus consists of small, +branched filaments with intercalary growth, extending vertically from a horizontal, branched filament or disc, but sometimes it is reduced to this last condition only. Zoospores are produced by division (for fertilisation see Fig. 66) either outgrowths or arise by the transformation of one or several of the ordinary cells. The most common genera are: *Ectocarpus* and *Phyllospora*. + +Order 2. *Chondrus*. The thallus consists of a *Reconopodium*. + +Order 3. *Spiroclariaceae*. + +The thallus consists of small, +parenchymatous, more or less ramified shoots, presenting a feathery-like appearance. +In the shoots, within the cortex layer, surrounding a row of central cells, is present. Sporangia and gametangia are outgrowths from the main shoot or from its branches. *Spiroclaria*, *Chotophyta* are common forms. + +Order 4. *Enceliaceae*. *Pantheria*, *Aspero- +coccus*, *Pilophila fusca*. + +Order 5. *Striariaceae*. *Striaria*, *Phlo- +spora*. + +Fig. 68.—Axes of the thallus of Chondrus crispus. +Axis of Chondrus crispus. S Agri- +cal cell. + +PHOROPHORE. 71 + +Order 6. Dictyophoraceae. *Dictyophora*. Order 7. Desmarestiaceae. *Desmarestia atlantica* is common. +Order 8. Myriarchiaceae. *Myriarchis*. +Order 9. Chordatiaceae. *Chordatis* is a common epiphyte on species of *Fucus*. +Order 10. Chlorodiaceae. The aliot-systems are often surrounded by numerous, leaf-like appendages. *Lathraea difformis* occurs as roundel, brown-green masses of the size of a nut, generally attached to other Seaweed. +Order 11. *Lithothamnium*. *Lithothamnium* is common. +Order 12. Sperrmannaceae. *Sperrmannia paradoxa* is common. +Order 13. Sporocheniaceae. *Sporochne*. +Order 14. *Lithothamnion*. This genus is common as a red-brown incrusion on stones and rocks at the water's edge. +Order 15. Lithodermaceae. Some species of the genus *Lithodermum* occur in the North Sea. + +Order 16. Laminariaceae. The thallus is more or less leathery, and has generally a root-like lower part (fig. 69) which serves to attach it, and a stalk or stem-like part, terminated by a large leaf-like expansion. Meristematic cells are situated at the base of the leaf, and new leaves are derived from them. +The older leaf has pushed away by the intercalary formation of the younger ones, so that only one or two are wanting. Zoosporangia are developed from the lower part of a simple, few-celled sporangiole, which arises from a surface-cell and has a large club-formed apical cell. The sporangia are aggregated into closely packed groups at the upper part of the terminal leaf, or occur on special, smaller, lateral, fertile fronds (*Alaria*). Most of the species are adapted to live in seas of moderate or cold temperature and occur in the most northern regions that have yet been visited by foreigners, but they do not appear to be very important in the production of reproduction during the cold and darkness of the arctic night. +*Laminaria* is destitute of a midrib and has only one terminal leaf. + +Fig. 69.—Laminaria digitata (much re-enlarged), showing zoosporangia through a meso-sporangiole ; A para- meristematic cell. +h + +72 +THELOPORELLA. + +L. digitata has a broad leaf, which, by the violence of the waves, is torn into a number of palmette stripes (Fig. 60). L. sarcocarba has a small, undivided leaf. Almost all the mirids and special fertile fronds. *A. aculeata* occurs plentifully on the west coast of Nor- way and on the shores of Great Britain. *Chorda filum*, a common seaweed, grows in the North Sea, in the Baltic, and on the western coast of Ireland, without any strong demarcation between stalk and leaf. +Some attain quite a gigantic size, e.g. *Macrocystis pyrifera*, whose thallus is said sometimes to be more than 300 metres in length. The *Leucosmyxa*-species, like the above, form submarine forests of seaweed, which grow along the coasts of South America, the Cape, and other localities in the Southern Hemisphere. + +*Utric*. The large Laminariales, when they occur in great numbers, are like the Fucii, used for various purposes, for example, in the production of iodine and salt, and as an article of food (*Laminaria saccharina*, *Alaria esculenta*, etc.). *Laminaria* is employed in the preparation of a kind of syrup; in surgical operations it is employed for the distension of apertures and passages, as for instance the ear-pore; and in medicine it is used as a diuretic. In *Laminaria* and *Fucus* cell-walls, that they are employed for this purpose. The cell-walls are divided into two parts by a thin membrane (Fig. 61), which is called the *intercellular substance*—which shrivels up when dried, but can absorb water and swell to about five times its size. The status of *Laminaria* sensu stricto is doubtful. + +Order 17. *Cutleriaceae.* The thallus is formed by the union of the originally free, band-shaped shoots. The growth is inter- cellular by means of reproduction by the confluence of male and female gametangia. The sexual generation of different appearance, which produces zoospores, arises from the germination of the zygote. Cutleria, Zonariopsis. + +Sub-Family A. *Acinetaceae.* +Branching simple filaments with interbranchial growth. The organs of reproduction are partly uni- and partly multi-cellular; in the unicellular one cell without cilia is formed, which may be destitute of a cell-wall, but has one nucleus (oesophere ?), or which has a ciliated cell-wall (Fig. 62). In the multicellular, monosporous swarm-cells with two cilia (spermatoroids ?) are formed. The fertilisation has not been observed. + +Order 1. *Tlopteridaceae.* Haploconia, Tlopteria. + +CYCLOSPOREX. 73 + +Family 2. Cyclopsorex. + +The individuals are multinucleate, with growth by an apical cell. The thallus--often bilateral--is differentiated into a root-like structure (attachment-disc), and stem, sometimes also into lateral branches. The thallus is covered with a thin cuticle, or various tissue-systems, viz., an external assimilating tissue, a storing tissue, a mechanical tissue of thickened, longitudinal parenchymata, strengthening cells, and a conducting tissue of sieve-cells, or of chlorophyll-containing cells. The thallus is cylindrical, or flat, in Phycosporus. Vegetative reproduction can only take place by means of detached portions of the thallus (Sargassum), which are kept floating by means of bladders (Fig. 70 A, a; Fig. 72). Zoco- +spores are formed in the thallus. + +The sexual reproduction takes place by oogamous fertilisation. +The oogonia and antheridia are formed inside special organs (concep- +tacles), and are surrounded by paraphyses. The concep- +tacles are situated at the base of the thallus, and have apical depressions, produced by a specific ingrowth of the surface cells of the thallus and their mouths (ostioles) project like small warts; they are either situated near the end of the ordinary branches of the thallus (Fig. 70 B, b), or they are situated on short spines on this account (Fucus vesiculosus). The vertical section of a conceptacle is seen in Fig. 70 B, c (see also Fig. 71 b), where, in addition to the paraphyses, two large oogonia are visible. The oogonia is discoidal--male plant--yellow-brown; female plant; olive-brown; +but in some species antheridia, together with oogonia, are pro- +duced in the same conceptacle. The oogonia are large, almost spherical bodies, which are produced in groups of three or four; they are formed from 1–8 (in Fucus: S.; in Acrosporion: 4); in Halidrys: 1; in Peltaria: 2) rounded, immotile oospores. The wall of the oogonium ruptures, and the oospores, still enclosed in the inner membrane of the conceptacle, are released into the water, and float about in the water, being finally set free by the bursting of the inner membrane. The antheridia are oblong cells (Fig. 70 C, a), +many of which are produced on the same branched antheridio- +phores. They contain two nuclei each; these are surrounded with 2 chloro and are very small (Fig. 70 D, two antheridia sur- +rounded by spermatoids, one being open). The spermatoids, +still enclosed by the inner membrane of the antheridium, are + +74 +CYCLOSPOREE. +similarly set free, and fertilisation takes place in the water, +numerous spermatogonia collecting round the oosphere (Fig. 70 E), +which is many times larger, and by their own motion causing it to +rotate. After fertilisation, the oospore surrounds itself with a + + +A: A portion of a female conopeum ; b the mouth ; c the inner cavity ; +d an egg-cell ; e the outer wall of which the spermatogonia are escaping. +B: Fertilisation. +C: Germinating oospore. +D: Fuses viridales. +E: Portion of a female conopeum ; f the mouth ; g the inner cavity ; +h an egg-cell ; i the outer wall of which the spermatogonia are escaping. +F: Germinating oospore. + + +cell-wall and germinates immediately, attaching itself (Fig. 70 F) +to some object, and by cell-division grows into a new plant. + +CYCLOSPORAE. 75 + +Order 1. **Fucusæ**. The following species are common on our coasts: *Fucus vesiculosus* (Fig. 70) has a thallus with an entire margin, and with bladders arranged in pairs; *F. serratus* (Fig. 71) without bladders, but with serrated margin; *Anophyllum nudum* has a thallus with a long, narrow blade, and a pair of large, round bladders; *Halidrys siligenea* has its swimming bladders divided by transverse walls; *Humathalda toros*, which is found on the west coast of Norway, and the south coast of England, has a small perennial, button-shaped part, from the centre of which proceeds the long and sparsely branched, strap-like, annual shoot, which + +Fig. 71.—Scorpiusum barbiflorum. A portion of a male plant which has been exposed to the action of the open air for some time; small orange-yellow masses, formed by the exteriors, are seen outside the margins of the male compound leaflets. A cross-section through the stem shows the large air-bladders. + +Fig. 72.—Fucus serratus. A portion of a male plant which has been exposed to the action of the open air for some time; small orange-yellow masses, formed by the exteriors, are seen outside the margins of the male compound leaflets. A cross-section through the stem shows the large air-bladders. + +bear the conceptacles. The Gulf-wood (*Sargassum barbiflorum*, Fig. 73) is well known historically from the voyage of Columbus; it is met with in large floating detached masses in all oceans, and is found most abundantly in the Atlantic, off the Canary Islands, and in the Mediterranean Sea. The stalked, spherical air-bladders are the characteristic feature of this genus. The thallus is more highly developed than in Fucus, and there is a contrast between the stem and leaf-like parts. The + +76 +DICTYOTALES. +portions which are found floating are always barren, only those attached are fertile. + +Uses. The Fucus, like the Laminariales, are used as manure (the best kinds being *Fucus cerus* and *Acrosporium nudum*), for burning to pro- +duce kelp, and also for domestic animals (*Acrosporium nudum* is especially useful for this purpose). + +Class 9. Dictyotales. +The plants in this class are multicellular, and brown, with apical growth, new cells being derived either from a tip apical cell, or from a border of apical cells. The thallus is flat, leaf- or strap-shaped, attached by haustoria which are either found only at the base of the plant, or distributed over the whole thallus. The cells are differentiated into the following systems of tissues: an external, small-celled layer of assimilating cells, generally one cell in thickness, and an internal, large-celled layer of one or only a few cells in thickness, containing the reproductive tissues. All the reproductive cells are motionless. Asexual re- +production by naked, motionless spores (tetraspores) which are formed 1–4 in each tetraparenchyma, the latter being outgrowths from the surface of the thallus. In some species these tetraspores are wanting. The sexual organs are of two kinds, oogonia and antheridia, which are formed from the surface cells, either on the same or different individuals. The oogonia are spherical or oval, and are surrounded by a thin wall called the ectosporium or +oosphere, which on maturity is ejected into the surrounding water, and is then naked and motionless. The antheridia are formed of longitudinal cells, united in groups, whose contents by repeated division form a large number of spermatia which are divided into a large number of small, colourless, motionless spermatia round or elongated—which are set free by the dissolution of the wall of the antheridium. The process of fertilisation has not yet been described. + +The Dictyotales, in having tetraspores and spermatia, deviate considerably from the Phaeophyceae; but may be classed near to the Tetraeopterae, in which there are axonal spores with 4 cell- +nuclei, which may be considered as an indication of the formation of tetraspores. + +Order 1. Dictyotaceae. *Dictyota dichotoma* which has a thin, regularly dichotomously divided thallus, occurs on the coasts of the British Isles. +*Fucus* is found on the south coast. + +BANGIOIDEAE. +77 + +Class 10. Rhodophycæa (Red Seaweeds). + +The plants comprised in this class are multicellular; they are simple or branched filaments, or expansions consisting of 1 to several cells, or of a single cell (the thallus), as in *Fucus* (see also in *Porphyra*), to resemble stem, root, and leaf. The cells con- +tain a distinctly differentiated nucelus (sometimes several), and distinct chromatophores, coloured by rhodophyllin. The chloro- +phyll of the cells is green, but the colouring matter is more +or less red (phycoerythrin), which may be extracted in cold, fresh +water; or rarely by physocyanin. Pyrenoids occur in some. Starch +is never formed in the chromatophores themselves, but a modifi- +cation—Fucus-like starch—is found to be formed in the chloroplasts pro- +plastin. Asexual reproduction by motile zoospores (tetraspores) which are devoid of cilia and of cell-walls. Swarm- +spores are never found. + +Sexual reproduction is wanting, or takes place by the coales- +cence of a spermatium and a more or less developed female cell. +The spermatium are naked masses of protoplasm, devoid of cilia and +chromatophores. The female cell (carpospionum) is enclosed by a +cell-wall, and after fertilisation forms a number of spores, either +zoospores without cell-walls (carpospores), which grow into new +individuals. + +The Rhodophyceae may be divided into two families : + +1. HANDELMEDE. +2. FIGURE. + +Family 1. Bangioideæ. + +The thallus consists of a branching or unbranched cell-filament, +formed of a single row or of many rows of cells, or of an expan- +sion, one or two layers of cells in thickness, but without conspicu- +ous pores for the intercommunication of the cells. The growth of +the thallus is chiefly intercalary. The star-like chromatophores +contain red pigments, either blue (blue-green) or bluish-green, +or reddish with phycoerythrin ; all these colouring matters are +occasionally found in the same cell (Bangia-species). Asexual +reproduction by tetraspores, without cilia, but capable of amoeboid movement. + +Sexual reproduction is wanting, or takes place by the coalescence +of a spermatium with a carpospionum, which is only slightly differ- +entiated from the vegetative cells, and is devoid of a trichogyne. + +78 +FLORIDEE. + +The carposporae are ectoderm of cell-wall and arise directly by the division of the fertilised oospore. The Blastocystis occur chiefly in salt water. + +Order I. Goniotrichaceae.—The thallus consists of a branched cell- +filament without rhizoids. Tetraspores are formed directly from the entire contents of the oospore, and are generally produced in two divisions unknown. +Anatellus, Goniotrichum. + +The Goniotrichaceae, through the blue-green Algae, are allied to the +Myceliales, and are included in the order of the Phycophyceae. + +Order 2. Porphyriaceae.—The thallus is formed of an expansion consisting of a layer of 1-2 cells thick, which is extended to the substratum by means of a long, thin form of hapton (Porphyra, Dipterygium), filaments (very rarely slightly branched) filaments, attached at the base by haptera (Blepharostoma), and at the apex by a short, thick, unbranched hapton (crinoid). Tetraspores are formed after one or more divisions of the mother-cell, either from the whole or only a part of its contents; they possess sex-cells, sometimes with a stalked nucleus, and are often surrounded by a membrane having the same appearance as the vegetative cells, but divide several times, and several spermatia are formed, either simultaneously from the whole contents (Porphyra), or from a part of them (Blepharostoma). The latter contain the contents of the endosperm (Erythrotrichus). The carposporae in general have a trichogyne, but the conchus has a colourless spot which may no- +tions time rise into a long filamentous structure. The carposporae occur as an early stage in the development of the trichogyne. The spermatia form a small thallus, which is soon destroyed. The sex-cells consist con- +siderably with the spermatia in their colourless state. The fertilised oospore gives rise on germination into a number of carposporae, which are set free as naked, +multicellular masses of protoplasm, which grow and give rise to new individuals (alternation of generations). + +* * * Family 1. Florideae. + +The thallus has one or more apical cells, growing principally by apical growth, and may be branched like a root, stem, and leaf. +The chromatophores vary in form, but have a red or brownish +colour, due to chlorophyll and phycoerythrin. Asexual reproduc- +tion by motionless tetraspores, which generally arise by the +division of the contents of the oospore, is common among these plants. +The carposporae has a trichogyne, and the carposporae which are +formed indirectly by the fertilised oosporee, possess a cell- +wall. +The thallus may assume very different forms. In the simplest +species it is filamentous and formed of single, branched rows of +cells (Calothamnium, etc., Fig. 73). Ceramium has a filamentous +thallus, generally dichotomously forked (Fig. 75), or sometimes + +79 + +PLORIDEE. + +planately branched, which, at the nodes, or throughout its entire length, is covered by a layer of small cortical cells. *Polyphyllon* (Fig. 74) has a filamentous, much branched thallus, made up of a central cylindrical cell, surrounded by a layer of other cells, cortical cells, which in length and position correspond to the cortical cells of *Polyphyllon*. The two kinds of thallus organs are differentiated into stems and leaves, the former having, as in *Chora*, unlimited growth in length, whilst the latter soon attain their full development. *Chorda* has a feebly, gelatinous thallus, without nodes; it is repeatedly forked into flat branches of varying thickness. *Pleurocladus* has a forked thallus with thick branches and without nodes. The thalli of *Dichotoma* (Fig. 76) consist of branches, often bearing leaf-like structures on the midrib and lateral ribs springing from it. These ribs persist through the winter, and at the commencement of the succeeding period of vegetation the lateral ribs become the starting points for new ramifications, which are again divided into nodal and internodal. The name has been given to this genus from the fact that the thallus is incrusted with car- +bonate of lime to such a degree that it becomes very hard, and the + + +A: A small plant with numerous short axes of a branch with conocones (x 250). +B: A small plant with numerous long axes of a branch with conocones (x 250). +C: A small plant with numerous long axes of a branch with conocones (x 250). + + + +A: Polyphyllon serratum. +B: Polyphyllon serratum. +C: Polyphyllon serratum. + + +Figs. 73.--Collitiferae alpina : a plant with numerous short axes of a branch with conocones (x 250). +Figs. 74.--Polyphyllon serratum : a plant with numerous long axes of a branch with conocones (x 250), and without nodes ; b a plant with long axes and conocones ; c a plant with short axes and conocones. + + +80 +**FLOREDE** + +whole plant adopt a coral-like appearance. Other genera which are similarly increased, and have a leaf-like or even creosoteous thallus (such as Melobasia, Lithothamnium), are included in this family. + +In some instances the cells of the thallus may be found differ- +eolated into more or less well defined tissues, so that it is possible to find special assimilating, mechanical, and conducting tissues, the last named in some cases having the double function of con- +ducting and of serving as a reservoir in which starch is formed or +a reserve material. The cells of the Floreide, which are formed by +the division of a mother-cell into two daughter-cells of unequal + +Figs. 15.—Ceratium Rhizocarum (nat. size).—Fig. M.—Pelvetia (perforata) (School's size), have always larger or smaller pits in the cell-walls, and the thin cell-wall separating two pits from each other is perforated by a number of small holes. These pits are particularly developed in the conducting tissues, but sieve-tubes are very rarely to be found. +*Teltraperone* may be wanting (*e.g.* *Lemnaceae*) and often arise on special cells, but in most cases (*e.g.* *Teltraperone* sawan) only one teltrape is formed in each tetrapsonagonism, but the number is generally four, which may be formed tetrahedrally +(Fig. 73), or in a single row. The teltraperangia in some species are free +(Fig. 73), but in the majority they are embedded in the thallus. + +The sexual reproduction (discovered by Thuret and Bortot, +Copyright © 2023 by the University of Chicago. + +FLORIDEA. +81 + +1867) differs in the essential points from that of all other plants, and approaches most nearly to the sexual reproduction of the *Banyanoidae*. The sexual cells are developed from the terminal cells (never nodal) of the branched cell-filaments, which are arranged in a spiral manner. The cells of the spermatia (*permatangia*) are generally arranged in a group, the so-called *autheridia* (Figs. 74, 77 A, a). On becoming ripe the membrane of the spermatangium ruptures and the *permatia* emerge as spore-like ovules (called a little later they may possess a cell-wall) masses of protoplasmic material, which by means of the power of motion, and hence are carried passively by the current of the + +A small diagram showing a longitudinal section through a cystocysta ; a cystocysta with two *permatia*, one of which is in the process of division ; a cystocysta with three *permatia*, one of which is in the process of division. +Fig. 77.--A *Lecanis madurae*: *baryera*, longitudinal section through a cystocysta ; a cystocysta with two *permatia*, one of which is in the process of division ; a cystocysta with three *permatia*, one of which is in the process of division. + +water in which they may happen to be, to the female cell. This latter is analogous with the oogonium of the Green Algae. The female reproductive organ is termed the *procarpium*, consisting of two filaments (Fig. 77 b in A and D)—which contains the cell-nucleus, and an upper filamentous prolongation—the *triduomyne* (Fig. 77 B)—which is homologous with the *triduomyne* of the *Chlorophyceae* and *Porphyraeae*. In the sexual reproduction of the majority of the Florideae, a very important part is played by certain special cells, rich in cell-contents—the *auxiliary* + +82 + +83 + +FLORIDEA. + +cells. These are either dispersed in the interior of the thallus, or are arranged together in pairs with the cell-filament which bears the carpogonium, and are generally united with this to form an independent multicellular procarposperm. The spermatia attach themselves firmly to the trichogyne and surround them—nuclei of the spermatia being often found within the protoplast which is perforated, and the nucleus of the spermatium probably travels through the trichogyne to the swollen part of the procarposperm—the carpogonial sac and fuses with its nucleus. After fertilisation the trichogyne, without any further development, breaks off at the procarposperm, constituting the fertilised spermoecium, grows out and forms in various ways, first a tuft of spore-forming filaments known as gonidoblasts, and finally the carpogonium. These latter form a fertile thallus, which completes the germination of the sporope of Oedogonia (Oedogoniae) and Coelocotylus. + +The gonimoblasta may arise in three ways —— + +1. In the Nemoanellaceae, branched filaments grow out from the carpogonium and form an upright, compressed or expanded tuft of spore-forming filaments. +2. In the Cryptoneelaceae, several branched or unbranched filaments (gonidio-cespites) grow out from the carpogonium, and these fuse with each other by means of an auxiliary cell. The gonimoblasts are then formed from the single cells produced by the conjugation. +3. In the genus Rhizofluvienella the gonioecium conjugates with an auxiliary cell by means of a short obovoidal filament, and from this auxillary cell a gonimoblast is produced. + +The gonimoblasts, which sometimes in the early stages are naked, and afterwards invested with a cell-wall, are developed from the terminal cells (or protoplasts) of the carpogonium. They are usually composed of two parts: a basal part, which constitutes a part of the plant in which the carpogonia arise. These parts are called carpogonial and are either naked (Fig. 75 A), or covered by a cell-wall (Fig. 75 B). The second part is formed in different ways. On this account the Floridion were formerly divided into Gynoxomorpha (Braunochlamys, Neodendron, Gonidium, etc.) and Anoxo- morpha (Xerococcus, Leptosporum, Zetococcus, etc.). + +The Floridion are divided into four sub-families —— + +Sub-Family I. Nemoanellaceae. The fertilised carpogonia produce directly the gonimoblasta. + +Order I. Neomannellaceae. Algae of brackish water and living in fresh water. They lack trichogyne, and the very sparingly branched fertile filaments, composed of many rows of cells, grow out from a procarposperm, which consists of a single row of cells bearing branches. *Lemnae* *fertilella*, often found on rocks and stones in quickly flowing streams. + +A diagram showing the structure of a Neomannellaceae alga. + +83 + +Order 5. Helminthocladales. Tetragonium is generally wanting (a.p. in *Nassalia*) or arises only as one tetragonium (e.g. *Eutarchoglossum*) and it is only in Lignari that four or five tetragonia are formed. Chantreusis is a genus of the order, but its species are very rare and little known. + +Several other Chantreusidæ-forms, living in fresh water, are "proembryos" of species of the genus *Eutarchoglossum*. The germinating carpophore grows out into a long, slender, thread-like shoot which bears a terminal thallus, either solitary or in a small series, but when growing in shady situations presents a much greater development. These highly developed proembryos have been described as "proembryos of the order". They are found in the genera *Chantreusis* and *Lignaria*, both of which are aquatic plants, and in the genera *Eutarchoglossum* and *Tetragonium*, both of which are terrestrial plants which are developed singly in the epiphragm; in *E. exiguum* and *B. borealis* which do not possess their developed female reproductive organs, the proembryo is represented by a single cell, the "proembryo-cell", which is produced by the germination of a spore-plant arising from the end of an upright filament of the proembryo. + +The proembryos of *Chantreusis* and *Lignaria* are very similar to those of *Eutarchoglossum*. Those latter bear the sexual reproductive organs and also whorls of branches; the central row of cells is enclosed by cells growing from the base of the whorl, and these cells produce branches which grow outwards and are developed. In this alteration of shoots there is really no alternation of generation, since the proembryo and the shoots with the sexual reproductive organs arise from one cell. + +Several species of *Eutarchoglossum* have a bluish-green or vermillion colour. + +*Nemalion multifidum* has a browned thallus, slightly branched, which is often covered with a white film. + +Order 6. Chotangaceae. Galaxea has a thallus thinly incrustated with iron. + +Order 4. Gelidiaceae. Noceraria, Gelidium. +Sub-Family 2. Gigartinaceæ. The fertilised auxiliary cell grows towards the base of the thallus, producing a large proecium generally present. + +Order 5. Acrotyloideæ. Aetopodium. +Order 6. Gigartinaceæ. Gigartinaea, Phyllogorgia, Aetopodium; Chondrus; *Gigartina* and *Phyllogorgia* are common lichens on the coasts of Scandinavia and Great Britain. + +Order 7. Rhodophyllumideæ. Rhodophylla; Euchorda; Euphorbiaceae purpurea; *Rhodophylla* sometimes the centre of its branch may be modified into tendrils-like haptera. +Sub-Family 3. Rhodomyiaceæ. Rhodomyia palustris is the common species. +Order 9. Rhodophyceae. Rhodophyceae are a common order. +Lomentaria, Gloioplaca, Plocamium. +Species of this order are rare among marine angiosperms; $d.$ alate and $d.$ sinuses are harmless forms which are not uncommon. + +Order 11. Bonnemaisiaceæ. Bonnemaisia. +Bonnemaisia marina; Bonnemaisia marina; *Pogoniphora*, of which many species are to be found on the coasts of Great Britain, is an Elatinaceæ, rigidly branched thallus consisting of a central row of cells sur- + +84 + +FUNGI + +comprised by a varying number of cortical cells of similar size—the so-called "aphanorhiza". + +Order 13. Ceramiumaceae. Frusty Algae, often branched dichotomously, or unilaterally pinnate. Spermothamnus, Grifidella, Callithamnion, Ceramium, *Pistia*. + +Sub-Family 4. Cryptonemiales. The cells formed by the coalescence of the auxiliary cells and the cymbodium-basalium, produce the gametangia. These are surrounded by the auxillary cells and are situated singly in the thallus. + +Order 14. Chlorothamniaceae. *Chlorothamnus*. + +Order 15. Grattantellaceae. *Hypogymnia*, *Cryptothecium*. + +Order 16. Dumontaceae. *Dumitza*, *Dudungia*, *Dudungia*. + +Order 17. *Ceratophyllum*. A genus of which has dichotomy only branchial, round shoots, common on the coasts of Great Britain. + +Order 18. Rhizopodiaceae. *Polydesmum*, *Bisphragis*. + +Order 19. *Gymnosiphon*. A genus of which this order form crumb-like coverings on stones, mussel-shells, and on other algae, but are not them-selves incrusted; *Petrolia*, *Crassula*, *Pezodendron*. + +Order 20. *Lithothamnion*. A genus of which is entirely erect, branched Algae, thickly incrusted with lime, so that a few species (Lithothamnion, also called *Nailor's*) occur in fossilized comunities from Jurassic to Tertiary periods. + +Melodium, Lithothamnion, Lithothamnion, Corallina. + +Ussu. "Caruragen" is the thallus of *Chondrus crispus* (Irish Moss) and is used as food. It is a common article of food on the coasts of Ireland, and swellish (a jelly-like coating) is its official. Eudogonium palmarum is generally eaten as food in Ireland and in some places on the west coast of Norway; it is also used as food for sheep and hence is termed "Sheep-pen-sweed". Agar-Agar is a gelatinous substance; a species of *Eudogonium* and *Gigartina* growing in China and Japan. + +Sub-Division III. FUNGI. + +Mode of Life. The Fungi have no chlorophyll, and are thus unable in any stage of their existence to assimilate carbon; they must therefore live as saprophytes or parasites. There is, however, no strong evidence that they can exist in either con- currence as true parasites, but only attain their full develop- ment upon or dead plants or animals (*Echinella*, *Eupnum*). Many saprophytes may occasionally appear as parasites, and are then designated "facultates parasita" (*Mycetium candidum*, *Legiadiomium pustulatum*), in contradistinction to those which only + +FUNGI + +appear as parasites, "obligate parasites" (Mildew, Brand- and Rust-Fungi, Cordyceps). + +The parasites which live on the surface of the host-plant are termed epiphytic (Mildew, Funiculadion); and those living in its tissues are termed endophytic (Ustilago, Peronospora). Epiotic (Ovularia tomentosa) and endophytic (Coryne, Eutomophaea) are distinguished, in the same manner, as those which live on the surface or in the interior of animals. The Fungi designated pathogenic are especially those which produce disease in man. + +Most of the diseases of plants are attributed to the parasitic Fungi. These force their way into the host-plant by piercing the outer wall of the epidermis, as in the Potato-disease; or by growing through a wound, as in the Rust of Wheat; or they can only penetrate through a wound, e.g. Nectria. Some effect an entrance into the host-plant by the secretion of a mucilaginous knot or ferula, which softens and destroys the cell-walls (Sclerotium, Spongosporus). Mould Fungi secrete fermenta (enzymes), which, for example, convert cane-sugar into a sugar capable of fermentation. + +The relation of the parasitic Fungus to the host-plant is mainly of two kinds: either the protoplasts are destroyed, or the protoplasm is killed, and the cellular tissue becomes discoloured and dies (Peronospora, Armillaria mellosa, Polyporus); in the other case, the parasite has an irritating effect on the cellular tissue so that it becomes larger than normal, producing hypertrophy. Such malformations are termed Fung.-galle (Mycoccidus): in this manner "witness brooms" are produced by *Bacillium*, "pocket-plants" by *Tolypium*, "honey-combs" by *Armillaria*, and "mushrooms" by *Peziza* *candida*. This hypertrophy may either be produced by a rigorous cell-multiplication, which is most frequently the case, or by the enlargement of the individual cells (*Syncytium*, *Calystegia*). The hypertrophy is often accompanied with the Lichenes is of a very peculiar nature, termed "mycoidum." + +**Vegetative Organs.** The vegetative parts of a Fungus are termed its mycelium. ¹ This is formed of a mass of long, cylindrical, branching filaments called hyphae (singular hypha), which have a continued apical growth. The mycelium, in its early development, shows a well-marked difference between the + +83 + +¹ From the Greek ἀπλος=Fungus, hence "mycoidum." + +86 +FUNGI + +two main groups of true Fungi: in the Phycomyces, or Algal Fungi, the mycelium has no transverse walls, and is therefore unicellular, while in the Mycomytes and Mycomycetes it is pro- +vided with dividing walls, which gradually arise during growth, in the youngest hyphae; intercellary transverse walls may also be formed at any time by the mycelium. In the Rust-Fungi (Ustilaginaceae), connections may be formed between two contiguous cells of the same hypha, by a protuberance growing out from an upper cell just above the transverse wall, and forming a junction with the cell below. These are known as clampsomycetes, +and appear to be of use in maintaining continuity be- +tween the two cells. + +The hymenium of Fungi, where they come in contact with each other, often grow together, so that H. forerun combinations (to- +sia) are formed, which may lead to very compact fleshy tissue. +When the hyphae are not only closely interwoven, but also united and provided with many transverse walls, the mycelium assumes the appearance of a tissue with homogeneous cells, and is then termed parenchymatous. The outer layer is usually a +mesh thickened, and composed of several layers, and the external layers, by the absorption of water, may often swell very much and become mucilaginous. In some instances the walls are colour- +less, or in other cases they are coloured in various shades. +The cell-contents may also be coloured, and in this case are gen- +erally yellow; this colour is chiefly connected with the fat (oil) +which may be found in abundance in the Fungi, whilst starch is +increased in quantity. + +The mycelium assumes many different forms; sometimes it appears as a thread-like, cobwebby, loose tissue, less frequently as firm strands, thin or thick membranes, horseshoe-like plates or tuber- +like bodies. Sometimes it is intercellularly distributed; sometimes it be +intercellular or intracellular according as it only extends into +the interstices between the cells or enters into the cells proper. +In the first case there are generally found haustoria, or organs of +section (cuticle), which are always present among the Ustilaginales +has no haustoria); but haustoria are also found among the epiphytic Fungi (e.g. Erysipheaceae). Intracellular mycelia are found in the Rust-Fungi, in Claviceps purpurea, Endogonaceae, etc. +In spite of their great diversity of form and structure they all live, +owing to the circumstance that it continues to grow per- +ipherally, while the older parts gradually die off ("fairy rings"). + +**FUNGI** + +87 + +*String-like* mycelia may be found, for example, in *Phallus*, *Coprinus*, and are formed of hyphae, which run more or less parallel to each other. *Membranous-like* mycelia are chiefly to be found in Fungi growing on tree-stems (Polyporaceae and Agaricaceae); they may have a thickness varying from that of the finest thread to several millimeters, and extend for several feet. The peculiar horny or leather-like strands and plates whilst, for instance, appear in *Amanita muscaria*, are known as *schlerodria*; they are found in the *Alga*, and often fifty feet. The tuber-like *Ceratium* or *schlerodria* play the part of nourishment, since a store of nourishment is accumulated in them, and after a period of rest they develop organs of reproduction. The sclerotia are hard, spherical or irregular bodies, from the size of a cabbage seed to that of a hand-bowl. They are white, brown, black, pseudo-parthenocytinum, external layer. Schlerodia only occur in the higher Fungi, and are found both in asperophytes, e.g. *Coprinus* parasiticus, e.g. *Clavaria* (Fig. 8), *Sarcoscyphus* (Fig. 9). + +**Reproduction.** Sexual reproduction is chiefly among the lower Fungi but near straight to the Algae, the Algæ-Fungi, and takes place by the same methods as in the Algae, namely by conjugation and by the fertilization of the egg-cell in the oogonium. + +The majority of Fungi have only sexual reproduction. The most important methods of this kind of reproduction are the sporangio-fertilization and the conidio-fertilization. + +In the *Fungi Imperfecti* (the *Ascomycetes* and *Basidiomycetes*) arise inside a mother-cell, the sporangium (Fig. 80). Spores without a cell-wall, which move in water by means of cilia and hence are known as *swarmspores* or *zoospores*, are found among the Oomycetes, the sporangia in which they swim about being called swarm-spore-sporangia (Fig. 80; Sg. 91; 94). + +In the *conidio-fertilization* the conidia (exopores) arise on some special hyphae (condiophores), or directly from the mycelium. When condiphores are present, the conidia are developed upon these hyphae; when not present, they arise directly from the mycelium (in many Fungi, for example in *Penicillium*, Fig. 111; *Erythraea*, *Cystopus*, or aceroplastically (in which method the chains of conidia become separated from one another by partitions-walls [Fig. 112]; *Pseudocystopus* [Fig. 113]; *Cylindrosporoides*). All conidia are at first unicellular; sometimes at a later stage they become two-celled or multicellular through the formation of partition-walls (*Poptophyllum*). The conidia with + +88 +Fungi + +thick, brown cell-walls, and contents rich in fats (vesting coenidia), can withstand unfavorable external conditions for a much longer period than coenidia with thin walls and poor in contents. + +The *stelangia* arise either from the ordinary cells of the mycelium (*Pseudomycetes*), or are borne on special hyphae. They are generally club-shaped, but in some species they are cylindrical or club-shaped (*Ascymyces*), more rarely they are cylindrical or spindle-shaped. While among the Pseudomycetes the size, form, and number of spores are indefinite in each species, in the Ascymytes the sporangiophores (axi) have a definite size, form, and number of spores. The spores of the Ascymytes are known as ascospores. + +The sporangial-fruitification is found under three main forms. +1. *Free Sporangia*, which are either single (Mucor, Fig. 78.), or branched (Thaumatomycetes, Fig. 103). +2. *Sporangial-Layers*. These are produced by a number of sessile or short-stalked sporangiophores, being formed close together like a panicle (*Tuberites*, Fig. 103). +3. *Sessile Sporangia*. These are usually small masses of many sporangiophores enclosed in a covering; they are found only in the Carposci, and are also known as *ascocarps*. The parts of an ascocarp are the covering (*carposid*), and the ascocystes, which is in contact with the inner wall of the covering. The latter consists of a layer of mucilaginous and sterile, slender hyphae. The latter either penetrate between the axi and are branched and multicellular (*paraphyses*, Figs. 103 d, 125, 126, 127), or clothe those parts of the inner wall which bear the ascocystes (*epithelial*). The latter may be simple or branched (e.g. *Chromatium*, *Sordaria*, *Stictochytrium bohemianum*). The ascocystes are produced directly from the mycelium, or from a stroma, that is a vegetative body of various forms, in which they may be enclosed (Fig. 125 b). + +Among the coenidiophores these are, in the same way, three divisions. + +1. *Free Coenidiophores* (Fig. 109). The form of the coenidiophore, the shape, number of its spores are various. In the most highly developed Fungi, the Basidiomycetes, there are, however, special more highly developed coenidiophores, the *basidia*, which have a definite form and spores of a definite shape and number. The coenidiophores here have also cellular walls. + +2. *Conidial-Layers*. (The *conidial* case of this is found when the conidiophores arise directly from the mycelium, parallel + +FUNGI 89 + +to one another, and form a flat body (e.g. *Eucharidium vaccinii*, *Hypocrea* among the Phycomyces, *Bryum muscorum* and *Cytogonum*). (b) In *A. hygrometricum* the conidiol layers are thick, filled threads (stroma) inserted between the mycelium and the hymenium (i.e. the region of the conidia), and in *A. hygroscopicum* found in the section of the pileus (Fig. 122). (c) The mushroom form has the basidial-layer, that is a conidial-layer with more highly developed conidiophores (basidia). The basidial-layer, with stroma, and the hymenium (of the basidium), forms the basidio-fructification, which is branched or unbranched. The basidio-fructification is in other Hymenomycetes (in these groups the hymenium is confined to the lower side of the pileus). + +The hymenium of this basidial-layer and basidial-layer is composed of conidiophores, or of conidiophores and sterile hyphae (paraphyses) which are probably always unicellular. Paraphyses are found in *Endomphalotrichum radicans*, and in certain Basidiomycetes, e.g. *Coriolus*. + +3. CONIDIOPHORES (pseudocilia). A special covering surrounds the conidiiferous elements. The inner side of this covering (*peridium*) bears the hymenium, i.e. those elements from which the conidia are abscised. The basidiocarps arise either immediately below the hymenium, or they are embedded in the mycelium, or generally embedded. Conidiophores are entirely wanting in the Phycomyces and Basidiomycetes, and in the latter group the conidiophores are known as *basidiospores*. The *Basidiospora* increase (basidia) and are known as *basileocarps*. Conidiophores with simple conidiophores are found only among the Basidiomycetes, in the Cnidaria, and in *Ceratocystis cornea*. In the Ascomycetes (Figs. 120-122) there are two kinds of conidiophores: on one hand, points, to the naked eye, while the basidiocarps of the Basidiomycetes (Figs. 170, 171, 173-176, 178-180) vary from very thin to that of a child's head. The "sporomoma" of the Ascomycetes is a conidiophore with a large number of conidia ("micoroidia") which germinate sometimes more slowly than other conidia. There is good evidence for considering these as male reproductive cells, called spermatia. + +The spore-forming structures are primitive structures. The comparison of the sporangia and conidia among the Zygomycetes, and among the species of the genus *Peronospora* shows that the conidia are aberrant formations, and that they have arisen through + +90 +FUGGL + +the degeneration of the sporangium, which, by the reduction of its spores to one, has itself become a spore. + +In the genus *Thamnophyllum* and *Charalatidium* the gradual diminution of the sporangia, and the reduction of the number of spores can be distinctly followed. +In *Thamnophyllum* the number of spores is often reduced to one, which is free in the sporangium (Fig. 163). The sporangium is then transformed into a sporangiole, the spore is usually united with the sporangium, and the two become a simple body, the so-called conidium, which is in reality a closed sporangium. How close this resemblance is to that of *Chlamydosporus* and *Charalatidium*, and how different from that of *Thamnophyllum*, is seen from the fact that, in the final stage of *Charalatidium* the same whorl-form of branching appears as in the sporangial stage of *Thamnophyllum*. In *Charalatidium* the conidium is produced by a hyphal cell, which grows through out the former sporangium-wall (exospore), while Ch. *josefi* germinates directly from a hyphal cell. The latter is produced by a hyphal cell, which grows from Water-Algae and inherits the spores from them. On this supposition, as the Phycomycetes assumed a terrestrial mode of life, the sporangia would become closed-sporangia, i.e. conidia. But in this case also, as in *Thamnophyllum*, the sporangia would become baum cells, containing distinct-like spores, and would eventually become closed-sporangia, i.e. conidia. The conidia are terrestrial modified for life on land. In *Chlamydosporus* and *Heterosporus* however, the sporangia are still preserved, but in every instance they are adapted to terrestrial spore-distribution; their spores being free on account of the destruction of the sporangial wall. This is shown by their distribution through the air. For further examples of spore-distribution see below, p. 91-92. + +The reproduction of *Fungi* is accomplished not only by spores and conidia, but also sometimes by chlamydospores. These are developed from hyphae which have aggregated into a pro- +plasm into masses which are surrounded by a wall-cell and take on a resting condition in the form of a spore, and are able to germinate and produce carpospores. In the formation of the chlamydospores, hyphae grow out from the walls of the ex- +panse of the neighboring cells; in the undivided hyphae of the Phycomycetes transverse walls are formed, and finally the chlamy- +dospores are set free by the decay of the empty cells connecting them with each other. One must distinguish between older +and free chlamydospores; these are those which have grown out, +which are cut off from the ends of hyphae (Fig. 162, 164), +and which serve for propagation in the same manner as spores. In *Chlamydosporus* reccescent the chlamydospores grow out into the air and fall down again; in *Heterosporus* they remain in +cistets they only germinate vegetatively, and not with the forma- +tion of fructifications. From *Chlamydosporus* up to the Auto- +basilmycetes the successive development of the fructification, + +A diagram showing stages in the development of a chlamydospore. + +FUNGI 91 + +which is interrupted by the formation of the chlamydospores, degenerates more and more. Among certain Ustilagineae the chlamydospores (hard-spores) no longer germinate with the produc- +tion of fructifications; in the Uredinales, only one of the three chlamydospore types is capable of producing fructifications on germination; the other forms only germinate vegetatively, like ordinary spores, and in the same manner as the chlamydospores of the *Austobasidiomyces*. In the Hemibasidii, and the Uredi- +nales, all three chlamydospore types are used as means of reproduction. They are found also among the Ascomycetes. + +The sporangia and the conidia of the Fungi have their common origin in the sporangiospores of the Phycomycetes. The sacci (and sometimes also the basidiospores) are descended from the sporangio-forming, lower Fungi; the basidia (and the Basidiomycetes) from those which bear conidia. The sporangia of the Phycomycetes are the primitive form and the start- +ing-point of all higher Fungi. The spores of higher Fungi, chy- +spores appear besides in all classes of Fungi as supplementary forms of reproduction, and are of no importance in determining relationships. Although the expression "fruits" must essentially be understood in this sense, it is customary to use the term "fruit-forms" is employed to designate the forms or means of reproduction of Fungi, and the organs of reproduction are known as organs of fructification, the sporangiophores and conidiophores respectively (see p. 308). The sporangiospores, conidiophores, +and basidiospores (see p. 309) are fruit-bodies. + +The majority of Fungi have more than one method of reproduction, often on various hosts (Uredinales). Species with one, two, or more than two methods of reproduction are called polyphyletic. Species with one method of reproduction are monophyletic. Monophyletic e.g. the Tubercularia; dimorphic: Mucor, *Fusio*- +tophaea, Saccharomyces, *Penicillium* *cruriforme*, *Pseudos* *cerevisiae*, *Candida* *albicans*, *Candida* *tuberculosis*, etc., etc. Methods of reproduction: yeast-like conidia, free conidiophores, conidiomata with small or large spores. + +The liberation and distribution of the spores and conidia. +The spores and conidia, on account of their small size and lightness, are spread far and wide by currents in the air, but in addition to this method, insects and other animals frequently carry them away. This is especially true of free conidia, occasionally effected by the complete shrinking away of the conidiophore, but more frequently by abstriction from the conidi- +ophores, either by their gradually tapering to a point, or by the + +92 +FENOL + +dissolution of a cross-wall (generally of a unicellular nature). +The individual links of condicidainae are detached from one another in the same way, or often by means of small, intercalary cells, which are formed at the base of the individual links, and becoming slimy, dissolve upon the maturity of the spores. +Special hyphae, which are known as "hyaline hyphae," may be found. In Parosporeus the cylindrical fruit-body in the dry condition become strap-shaped and also twisted. These are very hygroscopic, and the changes of form take place so suddenly, that the spores are violently detached from their parent-plant. The peculiar squarish spores may be found in the sporangium. Each club-shaped hypha which projects from the body of the fly, bears a condium at its apex; a vacuole, which grows gradually larger, is formed in the interior contents of this hypha, and the pressure thereby gradually becomes greater until the vacuole bursts at its apex, and the condium is shot into the air. By a similar mechanism, the spores of many of the Agaricae are cast away from the parent-plants. In the case of Pilosella (Fig. 85) the entire sporangium is thrown out with great force. The outermost contrivance, the basal region of the sporangium having, by the absorption of water, been transformed into a slimy layer which is readily detached. Sphaeroblastus, a Gasteromycete, has a small, spherical fruit-body, which is covered with a thin film of slime when ripe, suddenly bursts, and the basidiocarps contained in it are forcibly ejected. + +The spores which are enclosed in ascus are, in some instances, set free from another cell (ascus) prior to their complete development (Elaphotheceus, Erodiomycet). In the case of the majority of the Pyrenomycetes and Truffle, the ascii swell by the absorption of water into a slimy mass, which gradually disappears, so that the spores lie free within them. In other cases (e.g., in some species of fruit-body decay), as in those which have no aperture (Peripatocerae, Taberacea), or the slimy mass, by its growth, is forced out through the aperture of the sporophore, taking the spores with it (Nectria). The ejecion of spores is usually accompanied by a sudden increase in number of Ascomycetes, and should many spores be simultaneously ejected, a dust-cloud may be seen with the naked eye to arise in the air from the fruit-body. This is the case in the larger species of Fomes. The spores are then suddenly exposed to a damp current. A distinction is drawn between a simultaneous ejection of all the spores contained in the ascus, and an ejection at + +FUNGL 93 + +intervals (anoxeous), when only one spore at a time is thrown out. +The first of these methods is the most frequent, and is brought about by the ascus being lined with a layer of protoplasm, which absorbs water to such a degree that the elastic walls are extended at times to double their original thickness, and, by bursting up against the pressure of the spores, a circular rupture is made at this point, and the elastic walls contract, so that the fluid with the spores is ejected. Special means may in some instances be found to keep the spores in suspension until they have been ejected completely. Thus, a tough slime may surround all the spores (Sac- cobolus), or a chain-apparatus, similarly formed of tough slime; or there may be a hooked appendage from each end of the spores which hooks into the apparatus of another (Cystobolus). The peristome, which surrounds the ascus in many Ascocorynes, also play a part in the distribution of the spores, by reason of the pressure they exercise. The ascus in some of the Pyrenomycetes, which are known as "spore-bearers," is provided with a thin external wall, through which the spores are forcibly ejected to such an extent that, without becoming detached from their bases, they reach the mouth of the fruit-body one at a time, burst and disperse their spores, and so make room for a newer succession. An ejection of the spores at intervals from the ascus is rare. This takes place for example in those fungi whose husks are hollowed out. The external wall, by absorption of water, at last becomes ruptured, and the internal and more elastic membrane forces itself out in the course of a few seconds to one of two or three times greater length than its original size. In other cases the spore is forcibly ejected from a narrow aperture at the end of the ascus. + +**Germination of spores (condita and chlamydospores).** In many spores may be found one or more germa-spores (e.g., thinnier plants) or a germ-tube (e.g., Fungi Imperfecti) or in the external membrane (teleostopes in Rust-Fungi), through which the germination takes place. Generally this does not occur till the spores have been set free: in some Ascomycetes germination occurs within the ascus (Zygomycetes, Sclerotia). The different ways in which these spores germinate may be classified into three groups. + +I. THE ORDINARY GERMINATION effected by the spore containing a germ-tube or germ-sac, usually developed on an exineule. In spores with a double wall it is only the inner membrane which forms the germ-tube. In swarmsperms a single wall is formed after the withdrawal of the cilia, and this, by direct elongation, + +A diagram showing the structure of an ascus with spores. + +94 + +FUNGI + +becomes the germ-tube. The protoplasm accumulated in the spore enters the hypha, which, in pure water, can only grow as long as the reserve nourishment lasts. + +2. **GERMINATION WITH PROTHALLUS** differs only by the circum- +stance that the hypha developed from the germ-tube has a very limited growth, and does not immediately develop into a mycelium, but produces conidia (Rust- and Brand-Fungi). This prothallus must only be regarded as an advanced development of a conidiospore. + +3. The **formation of conidia** consists in the production of outgrowths, very much constructed at their bases, from one or more places. Each of the conidia formed in this manner may again germinate and produce new outgrowths. In some nourishments present, a branched chain of such conidia is formed, from these are finally detached from one another. Yeast-like budding from the conidia are produced in various Fungi, e.g. *Aecoides*, *Pteleosporus*, *Cultigamia*, *Ascocyma*, *Tremellinae*, etc., and also in other fungi, where they are produced in a very short time after the formation of the conidium. The building conidium of *Eccobasidium* forms a “mould” on the nutritive solution. The yeast-like conidia are not to be con- +founded with the “Mycen-yeast” (comp. Mycoseorum). For Sac- +charomyces cerevisiae see page 108. + +In a compound spore (i.e. when a mass of spores are associated together) each spore germinates on its own account. There are sometimes, however, certain among them which do not germinate, but yield mycelium. + +The length of time for which conidia can retain their power of +germination is shortest (being only a few weeks) in those having thin walls and containing a large supply of water (*Peronosporaceae*, +*Uredinaceae*, *Ustilaginaceae*), and is longest in those which have +dry walls before they are able to germinate (resting spores). It has been observed in some spores and conidia, that the faculty of +germinating may be preserved for several years if the conditions necessary for germination remain absent (*Ustilagineae*, *Eriosema*, *Penicillium*). + +The optimum, minimum and maximum temperatures required for the germination of the spores has been decided in the case of +a good many fungi. In general, most fungi require temperatures +to have their optimum at 25°C, minimum at 1-2°C, maximum at +40°C. In the case of pathogenic Fungi the optimum is adapted to +the temperature of the blood. Fungi living in manure, whose + +**ZYGOMYCETES.** + +Spores are often adapted to germinate in the alimentary canals of warm-blooded animals, have an optimum corresponding to the temperature of these animals, but with a little margin. + +**Systematic Division.**—The lowest class of the Fungi is that of the Zygomycetes, which includes the Ascomycetes, Basidiomycetes, sexual and asexual reproduction, and have doubtless sprung from sporangia-bearing, lower Green Algae. From the Phycomycetes (and certainly from the Zygomycetes) spring two well defined branches, each of which has its own sub-class. The first is the *Hymenomycetes*, the *Hymeniales* and the *Ascomycetes*, to the other the *Basidiomycetes*. Ascomyces and Basidioyces may be united under the title of *Mycothecia* or *Heredi Fungus*. The *Hymeniales* include the *Hymeniales* and *Basidiales*. The Hemibasidii are an intermediate form between Zygomycetes and Ascomyces; the Hemibasidii a similar group between the Zygomyces and Basidioyces. Mycosemyces and Mycothecia have evolved from the *Hymeniales*; sexual reproduction is wanting. Their mycelium is multicellular. + +Up to the present time about 30,000 species have been described. Review of the divisions of the Fungi:— + +**Class I.—Phycomycetes (Algal-Fungi).** + +Sub-Class 1. Zygomycetes. +Sub-Class 2. Oomycetes. +Family 1. Eucystidiales. +Family 2. Mycosporales. + +**Class II. Mesomycetes.** +Sub-Class 1. Hemiasciidii (Brand-Fungi). +Sub-Class 2. Hemibasidiidii (Brand-Fungi). + +**Class III.—Mycomycetes (Higher Fungi).** +Sub-Clas 1. Acomyces. +Series 1. Ascocarci. +Family 1. Gymnoscales. +Family 2. Pyrenocarci. +Family 8. Pyrenocarci. +Family 4. Hymeniales. +Family 5. Basidiales. +Family 6. Helvelles. +Additional: Ascolichenes. +Lichen-forming Ascomyces. + +W.R. + +H + +96 + +**ZYGOMYCETES** + +Sub-Class 2. *Basidiomycetes.* +Series 1. *Prothalliospermicetes.* Partly gymnosporic, partly angiosporic. +Series 2. *Prothalliosporicetes.* +Family 1. *Dacynomycetes.* Gymnosporic. +Family 2. *Hymenomycetes.* Partly gymnosporic, partly hemi- +angiosporic. +Family 3. *Phallogomycetes.* Hemiangosporic. +Family 4. *Gasteromycetes.* Angiosporic. +Additional to the Fungi: *Fucus* *Isorecurvus*. Incompletely known +(*Saccharomyces, Oidium-forma, etc.*) . + +**Class 1. Phycomycetes (Algal-Fungi).**3 +This group resembles *Vesicularia* and the other Siphonae among the Algae. + +**Ordain of Nutrition.** The mycophylum is formed of a single cell, +often thrailed-like and abundantly branched (Fig. 75). Vegetative +propagation by chlamydoспорos and oidia. Asexual reproduction +by endospores (Fig. 76). Sexual reproduction by conjugation of two hyphae as in the Conidio- or +by fertilization of an egg-cell in an oogonium. On this account +the class of the Phycomycetes is divided into two sub-classes: +*Zygomycetes* and *Oycomycetes.* + +Sub-Class 3. *Zygomycetes.* +Sexual reproduction takes place by zygonia, which function +as resting-spore-producing cells during the vegetative conjugation (Fig. 81); in the majority of species these are rarely found, and only under +special conditions. The most common method of reproduction is by +endospores, by angiospore conidia, by chlamydospores and/or by oidia. +*Zygomycetes* are generally characterized by the presence of +zygonia (Fig. 80). The zygonia are generally produced when the formation of sporangia has ceased; e.g., by the suppression of the sporangial- +hyphen (*Mucor* *ascoid*) or by the diminution of oxygen; *Pseudalles* +*cystidiales*, *Pseudalles* *cystidialis*, and *Pseudalles* *cystidialis* are infected +with saprophytic *Fusarium* or *Platocarli.* + +A. Asexual reproduction only by sporangia. + +Order 1. *Mucoraceae.* +The spherical sporangia contain many +spores. The zygonia is formed between two unicellular branches +(gametalia).1 + +1 Also termed *Water-Fungi* (*Wasserpilze*). + +A diagram showing the structure of a zygonium in a Mucoracean fungus. + +EGYOMYCETES. +97 + +The unicellular mycelium (Fig. 78) of the Mucoraceae branches abundantly, and lives, generally, as a saprophyte on all sorts of dead organic remains. Some of these Fungi are known to be capable of producing alcoholic fermentation, in common with the Saccharomyces. This applies especially to Chlorogalum monosporum. A mycelium, which has been deprived of its solution, and deprived of oxygen; the mycelium, under such conditions, becomes divided by transverse walls into a large number of small cells. + + +A mycelium which is growing from one apex, whose position is marked by the *a*, *b*, *c* are three sporangia in different stages of development; *a* is young, *b* is middle-aged, and *c* is old. The young sporangium is constricted in form; a sporangium which is larger than *c* but yet not separated from its stalk. + + +Many of these swell out into spherical or club-shaped cells, and when detached from one another become chlamydospores, which abstract new cells of similar nature (Fig. 79). These chlamydospores are often mistaken for yeast-cells (page 94), but they must not be confounded with the yeast-cordin (page 94). They are shortened hyphae, and are not conidia of definite size, shape, and point of budding. Oidia are also found in Chlorogalmon. + + +A mycelium which is growing from one apex, whose position is marked by the *a*, *b*, *c* are three sporangia in different stages of development; *a* is young, *b* is middle-aged, and *c* is old. The young sporangium is constricted in form; a sporangium which is larger than *c* but yet not separated from its stalk. + + +98 +EUGONCETES + +The Mucoraceae, in addition to the chlamydospores and oidia, have a more normal and ordinary method of reproduction; viz., by *spore* which are formed without any sexual act. *Mucor* has round sporangia; from the mycelium one or more long branches, sometimes several centimetres in length, grow vertically into the air; the apex of which (Fig. 76) forms a sphere, which soon becomes separated from its stalk by a transverse wall; in the interior of this sphere (sporangium) a number of spores are formed; these spores are free by the rupture of the wall. The transverse wall protrudes into the sporangium and forms the well-known colutum (Fig. 76 A). The formation of spores takes place in various ways among the different genera. + +SEXUAL REPRODUCTION by conjugation takes place in the following manner. The ends of two hyphae meet (Fig. 81) and become more or less club-shaped; the ends of each of these are cut off by a cell-wall, and two new small cells (Fig. 81 A) are thus formed, these confluence and give rise to a new cell which becomes the very thick-walled zygote (zygospore), and germinates after a + +Fig. 76.—Chlamydospores of *Mucor*. +Fig. 76.—Chlamydospores of *Mucor*. + +Fig. 76.—Mucor sexus ; a *spore* commencing to penetrate (x 300 times); b a germinating spore which has formed a germ-tube from each end (x 300 times); c the apex of a young mycelium with a sporangium (x 300 times); d the transverse wall protruding into the sporangium in the form of a colutum ; on the wall of the sporangium is found a very thick layer of mucilage (x 300 times); e the formation of zygote by confluence of two hyphae; f the zygote; g the zygote germinating (x 300 times). + +In some cases, however, when the formation of zygote has commenced, c a sporangium, the wall of which is ruptured, having a remnant attached to the base of the colutum as a small oval. A few spores are seen still adhering to the colutum. + +Fig. 81.—Sexual reproduction in *Mucor*. A, B, C, D, E, F, G. +Fig. 81.—Sexual reproduction in *Mucor*. A, B, C, D, E, F, G. + +**EYGOMYCETES.** 99 + +period of rest, producing a new hypha, which bears a sporangium (Fig. 81 B). + +*Micros* *stercorale.* Fin- +mond, resembles some- +what in appearance +the *Fusarium* *solani* +and is found growing upon various organic +materials (manure, jem- +dung, etc.). + +*Fusarium* *solani.* +(Fig. 81, 83, +84) grows on manure. +Its sporangium (Fig. 84 +C) is formed at night and by a peculiar +mechanism (page 92) is +discharged during the +in the course of the day. +This generally takes +place between eight and ten +a.m. The sporangium +is spherical in shape, +which may be 500 times +greater than the body of +plant itself, and by its +stickiness it becomes +attached to other +plants, etc., are in the vicinity. If these +are not removed, +the spores pass into the + alimentary canal and +are eaten by the plant, +even in a germinating +seed, and passed out +with the excrement, +of which they form new +sporangia. + +*Pleosporum* *mitus* +(= *Oidium* *mitus*) +("Oil-mould") is that +species of *Fusarium* whose sporangiospores may attain the height of 10-30 m. +Order 2. Rhizopods. *Eriophyes nigriceps* (*Micros stolosifor*) which lives on degrading fungi containing sugar, on bread, etc., has, at the base of the sporangium, a short stalk with a knob-like structure, serving as a point of attachment. From these "runners" are produced which in a similar manner develop sporangiospores, and rhizoids. + +Order 3. Thallomycetes. On the same sporangiospore, in addition to a + +109 +**OOMYCETES.** + +Large, terminal, many-septate sporangium, many smaller, lateral sporangia are formed with a few spores. *Thamnomyces*. + +**B. Asexual reproduction by sporangia and conidia.** + +Order 4. *Chytridiomycetes*. *Chytridium* with creeping endoglyphic mycelium, and *Chytridium* sporophytes. + +Order 5. *Mortierellaceae*. *Mortierella* polyphthora produces on the same mycelium conidia and sporangiophores. *M. rostrata*, with long, stalked sporangiophores, which is surrounded at its base by a covering of numerous fleshy hyphae. + + +A: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +B: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +C: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +D: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +E: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +F: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +G: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +H: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +I: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +J: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +K: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +L: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +M: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +N: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +O: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +P: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +Q: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +R: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +S: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +T: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +U: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +V: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +W: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +X: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +Y: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +Z: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +AA: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +AB: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +AC: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +AD: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body (C). +AE: Aerial view of *Pleodiscus* mycelium (a, b) with a sporangiophore (A) and the fungal fruiting body +109 + +Sub-Class 2. **Oomycetes.** + +Sexual reproduction is oogamous with the formation of brown, +thick-walled coopes which germinate after a period of rest. +Axexual reproduction by conidia and swarmconidia. Parasites, +such as saprophytes. + +The coopes are large pores which are formed from the egg-cell +(coopeum), Fig. 80. 95). A branch of the mycetum attaches itself to the coopeum and forms at its base an apical projection ("polypodium"). This sends one or more slender prolongations ("fertilizing tubes") through the wall of the coopeum to the egg-cell. + +1 Anthurialum is preferred in this sub-class as keeping more uniform term (*Kn.*). + +CONTECETES. +101 + +A fertilization, a passage of the contents of the anthoridium to the egg-cell, has as yet only been observed in *Pythium*; in *Phytophthora* only one small mass of protoplasm passes through the fertilizing tube to the egg-cell; in *Peronospora* (fig. 85) — *Empusa* means (*Pyronemus*). I. A fly killed by the fungus, surrounded by a white layer of mycelium. II. The same, with the eggs. III. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. IV. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. V. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. VI. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. VII. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. VIII. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. IX. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. X. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +VII. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XII. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XIII. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XIV. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XV. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XVI. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XVII. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XVIII. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XIX. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XX. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XXI. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XXII. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XXIII. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XXIV. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XXV. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XXVI. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XXVII. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XXVIII. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XXIX. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to the brain. + +XXX. The same, with the contents of the anthoridium, a few of which have developed secondary anthoridia, attached to + +XXXI. +the brain. + +XXXII. The same, + +XXXIII. +with + +XXXIV. +the + +XXXV. +contents + +XXXVI. +of + +XXXVII. +the + +XXXVIII. +anthoridium, + +XXXIX. +a + +XL. +few + +XLI. +of + +XLI. +which + +XLI. +have + +XLI. +developed + +XLI. +secondary + +XLI. +anthoridia, + +XLI. +attached + +XLI. +to + +XLI. +the + +XLI. +brain. + +XXXIX. +The +same, +with +the +contents +of +the +anthoridium, +a +few +of +which +have +developed +secondary +anthoria, +attached +to +the +brain. +XXXX. +The +same, +with +the +contents +of +the +anthoria, +a +few +of +which +have +developed +secondary +anthoria, +attached +to +the +brain. +XXXXI. +The +same, +with +the +contents +of +the +anthoria, +a +few +of +which +have +developed +secondary +anthoria, +attached +to +the +brain. +XXXXII. +The +same, +with +the +contents +of +the + +103 + +102 +OCOTETZES. + +nogora and the Saprolinaceae syn protoplasms can be observed to pass through the fertilizing tube, so that in these instances parthenogenesis takes place: Saprolinaceae thorelli, etc., have generally even no anthoridia, but nevertheless form normal eggs. The egg is fertilized by means of self-fertilization spermatozoide is only found in Monoleptisphaera spharica. + +A. Asexual reproduction by conidia only. +Family 1. Entomophthorales. +The mycelium is richly branched. The family is a transitional step to the conidio-bearing Zygomycetes, since the spores of many members of this family are produced by conidiophores. + +Order 1. Entomophthoraceae. Mycelium abundantly de- +veloped. This most frequently lives parasitically in living insects, +causing their death. The conidiophores forming the conidal- +layer project from the surface of the insect's body, and carry +conidia, which is ejected with considerable force, and by this +means transferred to other insects. These become infected by +the entrance of the germ-tube into their bodies. The spirocha- +tum runs up against the surface of the bodies of insects and +germinates by splitting a germ-tube. + +Genus: Empusa has a good many species which are parasitic on flies, +moths, grasshoppers, plant-lice. The conidium emits a germ-tube which pierces the skin of its host, and then penetrates into the body of the insect by means of its body, by division or by penetration similar to that taking place in yeast, each of which grows and becomes a long unbranched hypha, which finally fills up the whole body of the insect and causes its death. Each of these hyphae projects through the skin, and abuts a conidium, which is ejected by a spore-gland situated at the end of the hypha. The spore-gland is so large which makes its appearance epidemically towards autumn on the common house-fly, and shows itself by the dead flies which are found on the windows and walls. In this way it spreads over all Europe. The conidium is a small oval alveolatum, broad, white bulb of hyphae between the abdominal rings, and are surrounded by a circle of whitish dust formed by the ejected conidia— +entomophthoraceous spores. The conidium is produced by a single cell in the insect's body, terminal of hyphae, which serves the purpose of holding fast the dead insects, the ramifications attaching themselves to the substratum; the conidiophores are very short, and consist of two cells only; one cell lies be- +tween the hyphae and the conidium divide into two layers, those which ter- +minate the hyphae suddenly expanding and throwing out the conidia into the air. +C. Asexual reproduction by zoospores or conidia. + +Family 2. Chytriales. + +In this family the mycelium is very sparsely developed or is +wanting. The entire plant consists principally or entirely of a + +**OOMYCETES.** 103 + +single zoosporangium whose zoospores have generally one ciliun. The resting-spores arise either directly from the zoosporangium, which, instead of forming zoospores, surrounds itself by a thick cell-wall; or they are formed by the conjugation of two cells (in which case they are spores, as seen above). Microscopic fungi, parasitic on plants (especially Algæ), are saprophytic ani- +mals, seldom on land plants. + +Order 1. *Olpidaceae.* Without mycelium. Swarmspores and resting-spores. + +In the *Olpidaceae*, the swarmspores, probably most frequently form thallomatae and thallomatae, are masses of protoplasm which may become a single zoosporangium or a resting sporum. *Olpidium reticulatum* occurs in *Trichum* genus—in the Spathularia plasmodium emerging from the swarmspores travels to the leaves of the host plant and there forms a thallomata, each of which will become a zoosporangium. *Symphytomyces anserens* is found on *Anemone nemorosa*; *S. mercurialis* on *Mercurialis perennis*; *S. anserum* on many plants; and *S. trichophorum* on *Trichophyton*. + +Order 2. *Rhizidiaceae.* Mycelium present. Zoospores and resting-spores. + +*Chytridium* (Fig. 86). *Olpidium* (Fig. 87) is bidentate; the one cell is the mycelium, the other the zoosporangium; found on insects. The species of *Chlorostigmarum* are intercellular parasites on march plants. *Pseudopha- rma* (Fig. 88). + +Order 3. *Zygochytriacae.* Mycelium present. Zoospores and resting-spores. The latter are the product of the conjugation of two cells (Fig. 85). + +Polyphagous *olpidae* on *Euphema viridis*. *Drophiptus pulposus* on spores of *Chloropodium.* *Edemiasis leproidea* on the Bout-root. + +Fig. 86.—*Chytridium laevis*. Zoosporangium a before, b after the liberation of zoospores. +Fig. 87.—*Olpidium macrocarum*: a mycelium; b swarmspore. + +104 +OOMYCETES. +Family 3. Mycosiphonales. +The mycelium is bladder-like or branched. Zoospores. Sexual reproduction by zoospores, which are produced in oogonia. The latter are formed, in some forms, by the anthorhizium. +Order 1. Anzygiaceae. A large order of fungi, well known for the construction of zoosporangia, oogonia, or anthorhizium. Lepidostomis is parasitic on Spargenia, etc. + +Order 2. Mycosporaceae. Almost entirely parasitic. The unicellular very long and abundantly branched mycelium lives in the intercellular spaces of living plants, especially in the green portions, and these are more or less destroyed and deformed in consequence. Special small branches (section-organ). + +A diagram showing the structure of a mycelium with zoospores. + +Fig. 98.--Phytophthora exsulens. A with smooth B with thorny zoospores; m and n the two conjoining sets. + +"Kanoforiae" are pushed into the cells in order to abstract nourishment from them. Both zoospores and conidia germinate either immediately, or they develop into sporangia with swarm-spores, having always two cells. Only one zoospore is formed in each egg-cell, and this is surrounded by a thin membrane placed egg-cell and the "periplasm" surrounding it; this is of a paler colour and on the maturity of the zoospore forms its thick brown, external covering. + +The Fungi-plant (Phytophthora infestans) is of great interest. Its thallus winters in the Potato-tuber; other organs for passing the winter, such as zoospores, are not known. When the tuber germinates, Fungia-hyphae penetrate the young shoot and keep pace with the growth of the plant until the end of the shoot. The conidiophores emerge through the stomata, especially on the under side of the leaves; they branch like a tree (Fig. 90), and + +105 + +appear to the naked eye as a fine mould on the surface of the plant. The disease soon makes itself known by the brown colouring of those parts of the plant which are attacked, and by their withering. An ovoid conidium arises at first by the formation of a dividing wall at the apex of each branch of the conidiophore + + +A: A conidium. +B: A conidium with egg-cell and autolysis. +C: A conidium with egg-cell and autolysis. +D: A conidium with egg-cell and autolysis. +E: A conidium with egg-cell and autolysis. +F: A conidium with egg-cell and autolysis. +G: A conidium with egg-cell and autolysis. +H: A conidium with egg-cell and autolysis. +I: A conidium with egg-cell and autolysis. +J: A conidium with egg-cell and autolysis. +K: A conidium with egg-cell and autolysis. +L: A conidium with egg-cell and autolysis. +M: A conidium with egg-cell and autolysis. +N: A conidium with egg-cell and autolysis. +O: A conidium with egg-cell and autolysis. +P: A conidium with egg-cell and autolysis. +Q: A conidium with egg-cell and autolysis. +R: A conidium with egg-cell and autolysis. +S: A conidium with egg-cell and autolysis. +T: A conidium with egg-cell and autolysis. +U: A conidium with egg-cell and autolysis. +V: A conidium with egg-cell and autolysis. +W: A conidium with egg-cell and autolysis. +X: A conidium with egg-cell and autolysis. +Y: A conidium with egg-cell and autolysis. +Z: A conidium with egg-cell and autolysis. +AA: A conidium with egg-cell and autolysis. +AB: A conidium with egg-cell and autolysis. +AC: A conidium with egg-cell and autolys... +AD: A conidium with egg-cell and autolys... +AE: A conidium with egg-cell and autolys... +AF: A conidium with egg-cell and autolys... +AG: A conidium with egg-cell and autolys... +AH: A conidium with egg-cell and autolys... +AI: A conidium with egg-cell and autolys... +AJ: A conidium with egg-cell and autolys... +AK: A conidium with egg-cell and autolys... +AL: A conidium with egg-cell and autolys... +AM: A conidium with egg-cell and autolys... +AN: A conidium with egg-cell and autolys... +AO: A conidium with egg-cell and autolys... +AP: A conidium with egg-cell and autolys... +AQ: A conidium with egg-cell and autolys... +AR: A conidium with egg-cell and autolys... +AS: A conidium with egg-cell and autolys... +AT: A conidium with egg-cell and autolys... +AU: A conidium with egg-cell and autolys... +AV: A conidium with egg-cell and autolys... +AW: A conidium with egg-cell and autolys... +AX: A conidium with egg-cell and autolys... +AY: A conidium with egg-cell and autolys... +AZ: A conidium with egg-cell and autolys... +BA: A conidium with egg-cell and autolys... +BB: A conidium with egg-cell and autolys... +BC: A conidium with egg-cell and autolys... +BD: A conidium with egg-cell and autolys... +BE: A conidium with egg-cell and autolys... +BF: A conidium with egg-cell and autolys... +BG: A conidium with egg-cell and autolys... +BH: A conidium with egg-cell and autolys... +BI: A conidium with egg-cell and autolys... +BJ: A conidium with egg-cell and autolys... +BK: A conidium with egg-cell and autolys... +BL: A conidium with egg-cell and autolys... +BM: A conidium with egg-cell and autolys... +BN: A conidium with egg-cell and autolys... +BO: A conidium with egg-cell and autolys... +BP: A conidium with egg-cell and autolys... +BQ: A conidium with egg-cell and autolys... +BR: A conidium with egg-cell and autolys... +BS: A conidium with egg-cell and autolys... +BT: A conidium with egg-cell and autolys... +BU: A conidium with egg-cell and autolys... +BV: A conidium with egg-cell and autolys... +BW: A conidium with egg-cell and autolys... +BX: A conidium with egg-cell and autolys... +BY: A conidium with egg-cell and autolys... +BZ: A conidium with egg-cell and autolys... + + + +Fig. 37.--Phytophthora alataeum. Mps. on leaf. + +Fig. 38.--Phytophthora alataeum (enlarged). Cross section through a small section of a Potato-leaf (the under side being upwards); a the epidermis ; b two condilioi ds projecting through a stoma; c a condilion; d the spongy tissue of the leaf; e the mesophyll. + +106 + +105 +GOMCETES. +(Fig. 90 z), and immediately underneath it another is formed, which pushes the first to one side, and so on. These contain some- +times germinate directly, and form a mycelium, but most frequently their protoplasm divides into many small masses, each of which becomes a pear-shaped zoospore provided with two cilia (Fig 91). +Water is required for their germination, and they are placed in a drop of water; the swarming-cells are formed in the course of a few hours. The +swarms about rain and dewdrops in the Potato- +fields, and are carried with the rain-water to the plants and to the tubers in the soil. The wind also very easily conveys the conidia to healthy Potato fields and infects them. +The enormous quantity of conidia may be found by the farmer who explains the rapid spreading of the disease; and the preceding makes it clear why wet summers are favourable to its existence. When the swarming cells germinate, they round off, and then surround themselves with a cell-wall which grows out into the hyphae, and passes through the epidermis of the host-plant (Fig 92). Having entered the host, a new mycelium is formed. This has been known since 1845, has been rampant in Europe; it has no doubt, been intro- +duced from America. It is now widely dis- +persed, in the home of the Potato-plant. + +Fig. 91.—Physophora infestans. e-e conidia de- +veloping in a drop of water; d-d young mycelium; +c-c two free-swimming swarm-cells. +Fig. 92.—Physophora infestans. Cross section +through a portion of a Potato-stalk. Two germinat- +ing centres are seen at the base of the pedicels, and the +mycelium penetrating the cells. + +Mimically-formed conidia emerge as a spherical mass and divide into swarming-cells. P. de Baryanae lives in the axillae of many differing flowering-plants, +which it eventually destroys.—Physophora is distinguished by the fact that the sparsely-branched conidioles bear symmetrical chains of + +107 + +**OOGYCELES** + +condida. Besides the Potato-fungus (see above), *F. fasti* belongs to this group; it develops copious very abundantly, and does great harm to seedlings of the Beets, Sycamore, &c. Fine threads of the fungus grow on the leaves of the Sycamore, and form a brownish-red condium on each of the most extreme ramifications. Many do great harm to their host-plants. *P. viticola*, on Vines, is a common fungoid, which grows on the roots of the plant, and is found in the following species of this genus: *P. sparsa*, on Roses; *P. pulcherrima*, on composites; *P. stenocera*, on Sallow-leaves; *P. perniciosa*, on eruciferous plants; *P. virens*, on Violets and Fuses; *P. schizochla*, on Haste; *P. violacea*, on the + +Fig. 86.--A fly overgrown with fungus. +**Fig. 86.--A fly overgrown with fungus.** + +flowers of Scallions; *P. radii*, on the exy-dorsal of Melilotus; *Coptotrypa (Allegro)* has the conidia developed in chains, which form a colline white layer under-neath the epidermis of the host-plant. *Coptotrypa canadensis*, on cruciferae plants, forms a white condium on the leaves, which is covered by a yellow film on the epidermis, and from this point the mycelium develops together with the host-plant; *C. colubris*, on the Leaves of Compositae. + +Order 3. **Saproplaginaceae**, *Water-Fungi*; which live as saprophytes on organic remains lying in water, for instance, on dead wood floating in lakes, and in which they may also make their appearance on living animals, being frequently found, for example, on the young trout in rearing establishments. + +**Protozoa** (Fig. 92).--The body is a long branched cell. It has one portion which serves as root, and lives in the substratum, where it ramifies abundantly for the purpose of absorption; another portion projecting freely in the water, and sending out hyphae on all sides (Fig. 93). The sexual reproduction takes place by swarm-ing of two cells (Fig. 94), in large sporangia; these swarms are gener-ally possess two cilia, and on germination grow into new plants. The entire proto- + +Fig. 95.--Diagnosis with two antarhita, delta rau-mer. +**Fig. 95.--Diagnosis with two antarhita, delta rau-mer.** + +108 + +**Mesomycetes.** + +*Plasm in the oogonium is formed into one or more coenocyes, without any surrounding "periplasm". The coenocyes may not be fertilized (p. 100), and then develop parthenogenetically.* + +Genus: *Saprobionta*, whose swarms pores disperse immediately after having left the sporangium, *S. ferox* is the cause of a disease in fish (*Salmo* *leuciscus*). *L. leuciscus* is a parasite of the *L. salar*. In the lower half ball before the mouth of the sporangium—*Leptosoma* has strongly im- +dented lips, forming a "linked" appearance. *L. leuciscus* is frequent in the waste matter of the *L. salar*, and is found in the stomach of the *L. salar*. By the greater development of its fertilizing process: the oophore, situated in an open oogonium, becoming fertilized by auto-mitotic spermatocytes, which are provided with a filium at the posterior end. + +**Class 2. Mesomycetes.** + +The Mesomycetes are intermediate forms between the Phy- +comycetes and the Hymenio Fungi. In the vegetative organs, and in the mycelium, they show characters common to both classes. The methods of reproduction, however, show the characters of the Phy- +comycetes, namely sporangia and conidiophores of varying size and with varying number of spores; definite and typically formed ascus and basidium are not present. Sexual reproduction is wanting. + +The Hymenio Fungi transition between these Phycomycetes and the Ascomycetes, the Hymenio Fungi (Brand-Fungi) form the transition to the Basidiomycetes. + +**Sub-Class 1. Hemiclasi.** + +The Hemiclasi are Fungi with *sporangia* which, although resem- +bling ascus, yet have not, however, a definite form and a definite number of spores. Heads endospores, conidia, chlamydospores and other similar structures. + +Order 1. Ascocaridaceae. *Aedonides rubescens* forms irregular, reddish-brown masses in the upper leaves from fallen Echees. It has free sporangia, which resemble ascus but are not so definite in shape and size as those of the definite shape and size of the spores. The formation of the sporangia takes place when the nutricy is nearly exhausted, and resembles that of the conidia, since it is produced by a transverse wall within the sporangium which becomes separated by a transverse wall. Within the sporangium numerous spores of cap-like form are developed, which are free through an opening at the apex. +Sporangia are produced on a stalk which is attached to a leaf-stalk, +continuing to develop as the first is dehiscing. Conidia and sporangia are not +formed simultaneously; the former may be considered as closed sporangia. +Other genera: *Pseudoporus* produce large masses of white mycelium on +the stems and leaf stalks of *Tulipifera* (Tulipiferae, etc.). These are lii + +HEMIBASIDIID. 109 + +ings consist of chlamydospores (resting-spores), which germinate and become free, anus-like sporangia, with numerous small spores. In nutritive solutions the spores are often seen, but they may take the form of a large, thickened ex- +**Egopodium**, and other Umbellifera. +Order 5. Thelebolaceae. The thelebolus sterocome, is found on the dung of +feral animals, and is a very common plant, which resembles and in their shape and regular construction, and in the ejection of spores. The covering encloses only one sporangium, even when the sporangia are close together. + +This order, by reason of the covering of the sporangium, forms the transition from the Hemiaspidi to the Carpoanii, while the two first supply an intermediate step to the Eucarci. + +Sub-Class 2. Hemibasidiid, Brand-Fungi. + +The Brand-Fungi (also known as Ustilagines) are Fungi with basidia-like conidiophores, which, however, have not yet advanced to a definite form or number of conidia. They are true parasites, whose mycelium spreads itself in the intercellular spaces of Flower- + + +A. A branch-branch developed in the middle of a hypha. +B. A branch-branch developed in the middle of a hypha. +C. A branch-branch developed in the middle of a hypha. +D. A branch-branch developed in the middle of a hypha. +E. A branch-branch developed in the middle of a hypha. +F. A branch-branch developed in the middle of a hypha. +G. A branch-branch developed in the middle of a hypha. +H. A branch-branch developed in the middle of a hypha. +I. A branch-branch developed in the middle of a hypha. +J. A branch-branch developed in the middle of a hypha. +K. A branch-branch developed in the middle of a hypha. +L. A branch-branch developed in the middle of a hypha. +M. A branch-branch developed in the middle of a hypha. +N. A branch-branch developed in the middle of a hypha. +O. A branch-branch developed in the middle of a hypha. +P. A branch-branch developed in the middle of a hypha. +Q. A branch-branch developed in the middle of a hypha. +R. A branch-branch developed in the middle of a hypha. +S. A branch-branch developed in the middle of a hypha. +T. A branch-branch developed in the middle of a hypha. +U. A branch-branch developed in the middle of a hypha. +V. A branch-branch developed in the middle of a hypha. +W. A branch-branch developed in the middle of a hypha. +X. A branch-branch developed in the middle of a hypha. +Y. A branch-branch developed in the middle of a hypha. +Z. A branch-branch developed in the middle of a hypha. +AA. A branch-branch developed in the middle of a hypha. +AB. A branch-branch developed in the middle of a hypha. +AC. A branch-branch developed in the middle of a hypha. +AD. A branch-branch developed in the middle of a hypha. +AE. A branch-branch developed in the middle of a hypha. +AF. A branch-branch developed in the middle of a hypha. +AG. A branch-branch developed in the middle of a hypha. +AH. A branch-branch developed in the middle of a hypha. +AI. A branch-branch developed in the middle of a hypha. +AJ. A branch-branch developed in the middle of a hypha. +AK. A branch-branch developed in the middle of a hypha. +AL. A branch-branch developed in the middle of a hypha. +AM. A branch-branch developed in the middle of a hypha. +AN. A branch-branch developed in the middle of a hypha. +AO. A branch-branch developed in the middle of a hypha. +AP. A branch-branch developed in the middle of a hypha. +AQ. A branch-branch developed in the middle of a hypha. +AR. A branch-branch developed in the middle of a hypha. +AS. A branch-branch developed in the middle of a hypha. +AT. A branch-branch developed in the middle of a hypha. +AU. A branch-branch developed in the middle of a hypha. +AV. A branch-branch developed in the middle of a hypha. +AW. A branch-branch developed in the middle of a hypha. +AX. A branch-branch developed in the middle of a hypha. +AY. A branch-branch developed in the middle of a hypha. +AZ. A branch-branch developed in the middle of a hypha. +BA. A branch-branch developed in the middle of a hypha. +BB. A branch-branch developed in the middle of a hypha. +BC. A branch-branch developed in the middle of a hypha. +BD. A branch-branch developed in the middle of a hypha. +BE. A branch-branch developed in the middle of a hypha. +BF. A branch-branch developed in the middle of a hypha. +BG. A分支developed在中间的hyph。 +BH. Branch-developed在中间的hyph。 +BI Branch-developed在中间的hyph。 +BJ Branch-developed在中间的hyph。 +BK Branch-developed在中间的hyph。 +BL Branch-developed在中间的hyph。 +BM Branch-developed在中间的hyph。 +BN Branch-developed在中间的hyph。 +BO Branch-developed在中间的hyph。 +BP Branch-developed在中间的hyph。 +BQ Branch-developed在中间的hyph。 +BR Branch-developed在中间的hyph。 +BS Branch-developed在中间的hyph。 +BT Branch-developed在中间的hyph。 +BU Branch-developed在中间的hyph。 +BV Branch-developed在中间的hyph。 +BW Branch-developed在中间的hyph。 +BX Branch-developed在中间的hyph。 +BY Branch-developed在中间的hyph。 +BZ Branch-developed在中间的hyph. + +Fig 36.—Eulogium recurvum. + +1 Coursantiae or portione de leaf de Ficus permuntorii by its mycelium; 2 branches or Hyphae with conidia emerging from each other; 3 one or more branches found four transverse walls at some distance from each other (Fig 36), and remaining unconnected with each other. + +It most frequently happens that this germ-tube enters into host at its most tender age, that is, during germination of seed; then mycelium then wanders about tissues shoot + +110 + +HEMIBASIDIIL + +during its growth, until it reaches that part of the plant where the spores are to be formed. The spore-formation takes place in the same way in all those species whose brand-spores are deve- +loped in the floral parts of the host-plant. Many Brand-Fungi have, +however, a more or less distinct mycelium, which is mycorrhizic to a certain part of the leaf or stem. Those organs of the host- +plant in which the brand-spores are developed often become strongly hyphothecated. In perennial plants the mycelium winters very often in the soil. + +The brand-spores are the winter resting-spores of the Brand- +Fungi. They arise in the tissues of the host-plant, which is often destroyed, and become free through the rupture of the epidermis; + +A diagram showing the stages of development of a basidiomycete. The diagram is labeled with numbers 1, 2, 3, 4, and 5. + +Fig. 67.—Dacnusia elatior. 1. A fruit-body, formed by a covering of shining hyphae, which incloses a mass of brand-spores, and is embedded in the substance of the host- +plant, 30 times natural size. 2. A germinating brand-spore, 300 times natural size. 3. The germ-tube emerging from the base of the brand-spore, 300 times natural size. 4. The young sporophore, 300 times natural size. 5. The mature sporophore, 300 times natural size. + +they are thick-walled, generally brown or violet, and very often possess some pustules or reticulate markings. Fruit-bodies, that is enclosed organs of reproduction, are found in few genera (Spha- +lotoca, Graphidia; Dacnusia, Fig. 67). In Tolytopsorium, Tuber- +cinia, Thycoporeum (Fig. 102), etc., the brand-spores are united into a bud of spores (Fig. 103), which is called a "sporangium" or +"chlamydospore," namely, as the foundation of conidiophores, by emitting a short germ-tube, i.e. a conidiophore ("promycelium"). The Ustulinaeaceae (Fig. 92, 93) have a short transversely decided conidiophore (Fig. 94), which is terminated by a short conidium (Fig. +95). The Coniothyriaceae (Fig. 96) have a long conidiophore (Fig. +the Prothodoidiomycetes). The conidiophores of the Tilletiaceae +are undivided (unicellular promycolia), and bear the conidia ter- +minally, and so resemble the basidia of the Autobasidiomycetes. + +4 + +HERBARIUM. +111 + +In Tilletia, Eutypula, Noorosmia, Tubericola, the brand-spores germinate and form basidia-like conidiophores with spindle-shaped conidia; their my- +1 +2 +3 + +Fig. 68. — Tubericola. 1, T. triastica. Hyphae, some of which bear conidia at the apex, forming themselves out between the epidermal cells on the under side of the leaf, 100 times magnified. 2, T. triastica. Conidium. 3, T. triastica. Basidiospores. The basidiospores are about to germinate; 500 times natural size. 3, T. pseudotriacis: various forms of conidium. On the other hand, produce later only single, sickle-shaped conidia, so that two kinds of conidia are found, as in a few Basidiomycetes. In some +brand-spores only germinate vegetatively and form a myce- +lium (as in Ustilago, Puccinia, con- +tusions of damp, etc.) where they live as saprophyte; the brand- +spores are produced by germ-tubes, and on these, grow +the conidia are produced by +germ-tube budding which grow +into mycelia only when the +condition is favourable. + +These conidia have not the +power of producing alcoholic fermentation; but occasionally, +our conidia, which are found +in the dung of herbivorous ani- +mals, are also formed by +conidia of Brand-fruit. + +The brand-spores, which are eaten by animals and passed in the +hays, pass into the dung and +are often multiplied by +very rich multiplication of +post-conidia. + +The conidia (also called +myces) are formed by the +germination of the brand- +spores in the mycelium of the perio- +soma. 3. Germinating brand-spor of U. cerus +with developed basidium; b another, with a coni- +dium attached to it; c another; d another; e another, +placed diametrically opposite to each other; f, for +tached conidium which are growing into hyphae. + +1 +2 +3 +4 +5 +6 +7 +8 +9 +10 +11 +12 +13 +14 +15 +16 +17 +18 +19 +20 +21 +22 +23 +24 +25 +26 +27 +28 +29 +30 +31 +32 +33 +34 +35A diagram showing the structure of a plant, including a flower, leaves, and stems. + +Fig. 100.—Tetilla frutic, a case of Plant in which all the proies are attacked by Rink- +bein., &c., but the proies are not destroyed. The proies are shown in the upper part of the +stamens, of the same diameter ; a b brand-spores ; f, h, k germinating brand-spores ; i, para- +nuclear nuclei ; j, k, m, n, o, y germinating mycelium-spores ; g h magni- +fied 600 times ; 54 300 lines.) + +A diagram showing the structure of a plant, including a flower, leaves, and stems. + +HEMIBASIDIAL 113 + +to termination; there is no fusion of nuclei, and therefore in this "fusion" there is no sexual act. + +On the other hand, *Gymnoglossum*. Conidiophores with transverse walls and lateral conidia. —Entomio (Fig. 99) generally develops its spores in the fertile organs of its host-plant, the ovary or anthora, where they arise from hyphae, and form a single layer on the surface of the organ. To this order belong U. aurea, parasitic on Osa; U. hordei and U. undula (U. aurea), on Burley; these are the usual cause of "Smut" on cereals. U. hypogaea, on the other hand, is a parasite on the roots of *Cerealia* et *Gliricera*. U. ceraria terminates the fruits of various species of *Carica* into black, dusty balls. U. ceratina develops its spores without poison in the anthora of *Pterocarya* and *Celtis*. The latter produces a large number of conidia into a blackish-mass. Among the largest are *E. grandis*, which extends its conidia to the nodules in the stem of *Phragmites*, and the Mainz Blight, *E. capitata*, which produces a blackish mass on the leaves of *Bromus* and *Aloes* of the Mainz. + +On *Oenothera*. Conidiophores unicellular, generally several conidia arise at their apices.—*Trifolium trilobum*, the Stinkhorn on Wheat (Fig. 100). The mycelium lives in Wheat-plants, producing its spores in the ovary after the fertilization of the flower. In this case, however, the spores are produced by the excretion of the external layer of the wall of the ovary, which remains essentially unaltered and encloses the closely packed, firm mass of spores (Fig. 100 d). The spores are produced in two layers, one above and one below the outer cover, and the ears show the presence of this Fungus by their erect position, and due wide separation of the clasp (Fig. 100 e). The unimportant odour of the stinkhorn is due to a certain amount of alcohol contained in its tissues. In this way, in like manner, its haustoria when it encloses the ripe spores, is the reason why it is so much sought after by children. In this way also, in like manner, the dis- seed grains are readily harboured together with the healthy ones, which become internal by the spores at their threathing. L. tenuis (Figs. 101) also occurs on Wheat-plants. + +Entomio (Fig. 95). A genus with numerous species which appear in spore on the leaves of the ho-4-plant, and Turbincula (Fig. 68), which makes brown spots on leaves of *Ceratonia*. E. ceratina produces white conidia upon the surfaces of the ho-4-plant; it has only one spore; the latter is produced together—Entomio (Fig. 101) has its spores surrounded by a membrane; it produces white colored brown spores. U. occluda, Rhyno-stem Blight, occurs on wheat-plants; it produces streaks in the stems and leaves of the wheat, and does considerable damage. + +A diagram showing three stages of a fungus life cycle. +Figs. 100—99.—Entomio. U. ceratina. A sporontal with unmodified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 400 times magnified 4 + +113 + +114 +**ASCOMYCETES.** + +Put on Onions. *C.* ridge forms large dark-violet swellings in the leaf-stalk and stems of Violae.—*Thysanophora* (Fig. 103) appears in seedlings of *Con- +volvulus* and *Astragalus*. + +As a means of protection against the Sun Fungi the leaves make their appear- +ance on the surface of the soil by the evaporation of the grains in a solution of blue +vinicil ($\frac{1}{2}$) for twelve hours, or better still, submerging for five minutes in +water heated to 58-50° C (Rennell's method) is employed. + +A diagram showing two stages of asexual reproduction in Ascomycetes. + +Fig. 103.—*Thysanophora*. 1, *T.* convolvuli, a ball of spores; cross-section of the bread-spore has emulsified a sporeless tracheoid conidium (× 250). 2, *T.* chnus, a ball of spores (× 300). + +**Class 3. Mycomycetes, Higher Fungi.** + +The **Mycomycetes** are not entirely aquatic in habit; they have +hyphae with transverse walls; sexual reproduction in only few +cases. The sexual reproduction takes place in very different +ways; by ascospores, basidiospores, chlamy- +dospores, and oidia. Swampsports are never found. +Two chief methods of reproduction may be distinguished, +and hence the class may be divided into two large sub-classes—(the +**Ascomycetes** (with sacs), and the **Basidiomycetes** (with basidia). +Sub-Class I. **Ascomycetes** + +The main characteristic which distinguishes the Ascomycetes is +the sac; a name given to a sporangium of a definite shape and +size, and containing a definite number of spores. This shape is + +ARSONOCETES. +115 + +generally club-like or spherical), the number of spores 8 (in some 2, 4, 16 or more), see Figs. 103, 105, 108, 110, 113, 116, 120, 121, 123, 129. + +In the lowest forms, the ascocarps, the ascospores spring directly from the mycelium without the formation of a fruit-body (i.e. ascocarp). In the higher forms, which contain many species, the *Carposci*, the ascii are united and form ascocarps which may be more or less enclosed (angiocarpic, hemiaugiocarpic, and probably gymnocarpic). + +Fig. 123.—Endogenous formation of spores in *Fusius confusus*. In the youngest ascii there is only one nucleus (a, c); d this divides into two (c'), and the division is repeated on each side of the original nucleus (b). The nuclei then become separated by a protoplastic wall and a cell-wall (b, b'). The protoplasts of the mother-cell is not entirely used up. + +The hyphae of the *Mycelium* in some remain free, in others they are filated together and form thick strands or flat, cushion-like bodies (conidiophores in particular) (see also Fig. 7 of the *Pyrenomycetae*). Some species form *ascocarps* (Figs. 116, 125). + +Asexual reproduction by means of *conidia* is known in many species of Arsonocetes. These are produced in large numbers and thus afford the most rapid means of distribution. The conidia may be produced on conidiophores (Fig. 109), in conidial-layers (Fig. 122), and often in conidiocarps (pycnidia, Figs. 120 d, e; + +116 +ANCORYCETES + +125 a ; 124 b). The conidiophores bear no analogy to the basidia. +(The question of the occurrence of sexual reproduction among the Ancorycetes has been discussed by Harper. Recently Harper has proved the fusion of a male and female nucleus in Sphaerotheca. In Pyronema, a fungus closely allied to Puccinia, in Figs. 103a and 103b, a trichogyne and anastomosis contain several nuclei. The former is a large cylindrical cell having the apex prolonged into a trichogyne, while the latter is a cylindrical cell which originates below the oogonium, its apex coming into close touch with the tip of the oogonium. The oogonium is absorbed at the point of contact, and the male nuclei then pass into the trichogyne, by which they enter the oogonium, and finally, entering the oogonium by means of a new cell-wall, the male nuclei conjugate in pairs with the female nuclei of the oogonium. The oogonium is now cut off by a new cell-wall formed at the point where the trichogyne enters, and a thickened acrogenous hypha containing the conjugated nuclei is produced. + +Fig. 103a.—Sphaerotheca canina. +A: A (oogonium) (and other) +reproductive organs); B: A (male) +cell from off from the main +cell; C: A (male cell) from +off from the main cell; D: +female cell from off from +the main cell; E: female +nuclei; F: male nuclei; +G: oogonium; H: oospore. +(From Harper.) + +Fig. 103b.—Pyronema confluens. A: Roots of three pairs of sexual cells shown from each side; B: Male cell from off from the main cell; C: Female cell from off from the main cell; D: new partial wall; E: fusion of the two nuclei of the trichogyne; F: new wall formed at point where trichogyne enters; G: acrogenous hypha containing conjugated nuclei; H: oospore. + +A diagram showing the structure of Sphaerotheca canina. + +A diagram showing the structure of Pyronema confluens. + +**EXOASCI.** 1164 + +gated nuobi. Those hyphae branch, and ultimately bear the nuobi at their extremities, the paraphyses arising beneath the ascocone.] + +In many species the ascospore germinates and form conidia immediately (Nectria cinabariae, Sclerotinia, Taphrina, etc.), sometimes while they are still in the ascus and before their ejection (Taphrina, Fig. 105). In many in- +stances, however, the conidium is formed after the ascus has been liberated, +time, produce yeast-comb., e.g. Taphrina. In many other cases the conidia arise from the peritubes of the ascorpor, or at any part of the mycelium. + +The genus Sclerotinia is remarkable for its peculiar mode of reproduction by means of its spores. The Sclerotinia species produce numerous conidia whose germination has never been observed. The formation of conidia and ascus sometimes takes place simultaneously, but more frequently the conidia are produced first, and are developed successfully in the same fruit-body ; in the ascocarp of *Dermat- ium fungulae* and *Sclerotinia sclerotiorum* the formation of conidia may take place without the presence of an ascus. The same is true of *Corynespora*, etc. +eterna), etc.). This relationship of the two forms of reproduction to each other is well illustrated by considering that both have descended phylogeneti- +cally from sporangia. + +Sometimes chlamydomycetes and oïdia also appear in the Ascomy- +cetes ; on germination, however, they do not, as in *Pseudomyceta*, form sporangia, and on this account cannot be distinctly distin- +guished from them. + +The sac is morphologically the highest form of reproduction and are always found at the close of the development of these Fungi; the accessory forms of reproduction are first developed, but a well-defined alternation of generations does not occur. + +In the Ascomycetes there are more than 11,000 described species, which can be divided into two series : + +Series I. EXOASCI. Only one order. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
Order.Family.Genus.Species.
1. Chlamydomycetes.Family I. Gymnosporaceae.n° 1. *Perforatella**Angiospora carniola*
Family II. *Perforatellaceae.*n° 2. *Perforatella**Angiospora carniola*
Family III. *Hydrosporaceae.*n° 3. *Hydrospora**Hemiangiomycete Carposa*
Family IV. *Diocystaceae.*n° 4. *Diocysta**Hemiangiomycete Carposa*
Family V. *Chlamydosporaceae.*n° 5. *Chlamydospora**Hemiangiomycete Carposa*
+ +Additional Anoxiales : Lichen-forming Anoxymyces. + +**Series I. EXOASCI.** + +Anoxymyces with free ascus; sometimes also conidia, chlamydo- +spores and oïdia. One order. + +**Order. Taphrinaceae.** Of the genera belonging to this order, +Taphrina, Endomyces, and Anoxiohloes, the first is most important. + +A diagram showing a flowchart or decision tree with various branches and nodes. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
I. 1875-1876.
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+ + + + + +F.o. 233.—The apex of the mesocarp (cyst) of Allium in longitudinal section. The embryo-formation has commenced at the bottom of the hollow cavity, and is seen to be a bud of the macrospore (pollen-grain) + pollen-cortex. + +soon separate is developed, but never more than one embryo attains full develop- +ment. As several aradigonia are contained in one and the same ovule, all of which may be fertilised, it is possible that several embryos may be developed in a seed (polyembryony), yet usually only one +embryo attains perfect development. + +At the same time that the embryo is being developed, other changes are taking place in the ovule, especially in the integument which ensues between the egg and foot. The embryo-sac grows, and the embryo-sac supplies the cells of the mesocarp. The seed + +A diagram showing the structure of a seedling. + + +248 + +CRYPTOGAMS AND PHANEROGAMS. + +is now formed, and it consists in its most complete development, as in this instance, of three parts: +(1) The egg-sac, which is formed by the enveloping integuments, +with the remainder of the tissue of the nucellus lying outside the embryo-sac (the macrosporangium). +(2) The endosperm or prethallium. +(3) The embryo. +The reduction in the ANGIOPHORES is carried to the extreme limit. In the embryo-sac (the macrospore) the nucellus by continued division produces a prothallium consisting of primordial cells (Fig. 254). These are arranged in two layers, the upper one of the embryo-sac (which is nearest to the sporophyte), the second layer of the "co-operating cells" (synergidal) and the third is the oosphere. Three others are placed at the opposite end of the embryo-sac and are therefore termed the "antipodal cells". Finally, a large cell is also formed, which is called the egg-cell, whose nucleus is large and whose cell-nucleus, the central definitive nucleus, lies in the centre of the embryo-sac. These primordial cells are the slight remnant of the protallium. The entire structure of the archegonium, with its neck and canal-cells, has disappeared, but these cells act just as before, but the indispensable oosphere. When fertilisation has taken place, and has been fertilised, and has commenced, the cellular divi- +sion continues until, on account of the formation of the embryo (Fig. 255), the synergidal and antipodal cells are reduced, and a cell-for- +mation takes place by a new process which emanates from the definitive nu- +cleus and by which a nutritive-tissue is formed. This nutritive-tissue, arises which may perhaps be considered as homologous with that found in the Gymnosperms. The dif- +ference is that the nutritive-tissue is formed in two parts with an intervening intermedium; the primary nutritive-tissue is first formed, and after fertilisation is absorbed, + +A diagrammatic longitudinal section through an antherozoid ovule shortly after fertilisa- +tion. It shows a single megaspore (a), a megasporangium (b), a nucellus (c), a megaspore (d), +anatropous ovule (e), a megaspore (f), a megasporangium (g), with its integumentary coverings +(h) and its pollen tube passing through the integument (j) to its apex. +3 + +**CRYPTOGAMS AND PHANEROGAMS.** + +with the exception of one cell, which continues the development and gives rise to the nutritive-tissue proper, which is formed in the first instance of a nutritive-cell, and later on of a cellular tissue; this nutritive-tissue formed in the embryo-sac is termed "endosperm"; in a few instances¹ a tissue which is derived from the nutritive-tissue of the ovule is termed "endosperm" or "pul- +sperm". In many plants the seeds, when ripe, contain a very rich nutritive-tissue, in addition to the embryo, for the purpose of its nourishment during germination. These are termed albu- +minous (endospermous) seeds, in distinction to the ex-albu- +minous seeds, in which the nutritive-tissue is contained in the +embryo itself, before it is completely developed, and used for its sustenance. + +In addition to the changes which fertilisation produces in the ovule itself, it also gives the imbertus to a series of changes in the entire shoot which bears the ovule. The perianth, stamens, and style, generally without, because the part they play is at an end ; the wall of the ovary grows and becomes the wall of the fruit (pericarp), and finally the whole plant develops into a seed, +as a consequence of fertilisation, is termed a fruit. It consists of two parts, the pericarp and the seeds, and according to the nature of the pericarp, the fruit is termed a capsule, nut, berry, or drupe. + +The flowers are divided into two classes : (1) those in which +the formation of the flower (although they may quite properly be termed "Flowering-plants"), because Equisetums and Lycopods have reproductive shoots as highly differentiated as those of certain Angiosperms; (2) those in which only one of the +**fextal generation** the characteristics are found—(1) in its great reduction; (2) in the transmission of the microspore (pollen- +grain) to the macrosporangium, and its germination, with the formation of a gametangium; (3) in that form of sporangium which is not differentiated into spermatangia²; (5) in the fact that the macrospore (embryo-sac) never leaves its spermatangium (nucellus); and further in the Angiosperms, (4) in the peculiar development of the nutritive-issues in two parts; and (5) in the great reduction of the **fextal generation**. + +As regards the **fextal generation** the characteristic feature is that this generation is formed whilst the spermatangium is still attached to the mother-plant, and for a long time is nourished by it; and that after the spermatangium has been separated from the + +¹ Euphorbs, Symphoranthus. +² Except in Cycads and Ginkgo. + +250 + +CRYPTOGAMS AND PHANEOLOGIA. + +mother-plant, it spends a longer or shorter resting-period as the embryo in the seed (developed by the testa), and does not make its appearance until the "germination" of the seed. In addition the shoot which bears sporangia undergoes greater modification than in the case of the Flowerless-plants. + +The Plantae are divided into two Divisions as follows— + +Division 4. Gymnosperme. The ovules, as well as the seeds, are borne naked on the surface of open carpels, or on the apex of a stem (ovary wanting). The pollen-grains are conveyed by the wind to the ovule and carried by drops of mucus, secreted by the microsporangium, A—the "anther," is wanting. The prothallium (the endosperm), which serves for the nourishment of the embryo, is formed before fertilization. The archegonia are en- +tailed in the upper part of the ovule-tube. The pollen-grains are + +"multilocular," i.e., they are always in three cells, a distinct prothallium, formed by 1-3 cells, and a larger cell which gives rise to the pollen-tube. + +Division 5. Angiosperme. The carpels surround the ovules and form a closed chamber (ovary), in which the ovules mature and ripen into seeds. The surface of a portion of the apex of the carpel is transformed into the "stigma," which, by a sticky fluid and also by hair-structures, is capable of retaining the pollen-grains. These are conveyed by insects, or sometimes by insects. The pollen-tube grows from the stigma, through the "conducting cellular tissue" (style), to the ovules. The pollen- +grains contain two cells, a vegetative and a free generative cell. The latter contains a nucleus with a large nucleolus, and one of which is the sperm-nucleus. The female prothallium, which is intended to serve as nutritive-fuse, is formed after +fertilization. Archegonia are wanting. + +A diagram showing the structure of a plant with an ovary containing an ovule. + +DIVISION IV. +GYMNOSPERMÆ. + +The following characters should be added to those already given on page 2:— + +The Gymnosperms comprise only trees or shrubs. The flowers are always anemocous and destitute of petals (except Cycas); the female flowers are the one which has no flowers. The male flowers are constructed on the same type as the cones of the Horsetails and Club-Mosses, and are most frequently long shoots (Figs. 243, 255, 260 A, 267 J) bearing a number of spiral or vertically-arranged leaves (Fig. 243). The ovule is sessile. The structure (see the orders). The *ovule* is orthotropic (except *Podocarpus* which is ananorpus) and projects from the carpel uprightly, inverted, or horizontally; it has usually only one integument (except *Cycas*), but in some cases two integuments are formed by part of the nucellus, so that the embryo-sac is placed below the integuments (Figs. 251, 264). The drop of mucilage which entices the pollen-grains dries up and draws the pollen-grain close to the nucellus—the pollen-chamber—in which the germination of the pollen-grain commences. + +In each seed, only one of the many embryos which are formed precedes the other embryos into maturity. In *Podocarpus*, however, and the embryo has one, two, or a whorl of several cotyledons. A vigorous primary root is developed on germination. The vascular bundles in the stem are arranged in a ring, and increase in thickness with age; they are surrounded by a sheath of parenchyma. The form bast (phloem) externally, and wood (xylem) internally with distinct annual rings, or in the *Dicotyledons*. Only certain of the Cycadeae deviate from this arrangement. The secondary wood is very uni- coral, and consists of a single layer of cells; in other cases it is bordered pita, but true vessels are wanting; this also indicates a relationship with the Pteridophyta (see page 202). + +The Gymnosperms are biologically lower than the Angiosperms; they are wind-fertilised, and without extra floral-secretaics. + +A diagram showing the structure of a gymnosperm flower. + +252 + +GYMNOSPERME. + +This Division embraces three classes: *Cycadee*, *Conifee*, and *Gnetee*. It is a doubt monophyletic, and has taken its origin from heteroporous Ferns, now extinct, most nearly related to the Ophioglossaceae and Marattiacae. The Cycadeae appear to be the oldest class of the division, and are closely allied to the Ginkgo. The Gnetaceae are more isolated. The Division is not continued into the higher Flowering-plants; it has evidently attained its highest development, and is now in a retrograde condition. The similarity which has been noticed between the *Cycadee* and the *Lycopsidæ* is only in analogous resemblances, and does not entitle one to suppose that there is a nearer relationship, or that the former take their origin from the latter. + +Class I. *Cycadee*. + +The stem is very rarely ramified. The leaves are large, pinnate, and arranged spirally on the stem, with the veins, infoliate percurrent. +There is only one order, the *Cycadaceæ*. In habit they resemble the Ferns, especially the Tree-Ferns (compare Figs. 207 and 256). The stem is tubercular (Fig. 288), or cylindrical (Fig. 265), but not very tall (as much as about 12 metres), and very + +For 256.—*Cycas circinata* (female plant). The corolla are seen hanging from the top of the stem. Three leaves with the basal leaf rolled up project almost vertically into the air; four others are seen at different angles. + +Rarely ramified. [In Ceylon, unbranched specimens of *Cycas* are occasionally branch in greenhouses.] + +The leaves are large, pinnate, and so closely together that no free stem-surface is left between them, and have only a slight sheath (which is not amplexical), as in the Palms. They are com- + +CYCADAE. 253 + +pound (most frequently pinnate; in *Bocconia*, bipinnate); in some genera the leaves are rolled up in various ways, including the vernation of *Cycas* (Fig. 257); they are leathery or perennial. In some, stipules are present, as in the *Mastichaceae*. Groups of scale-leaves are found in the majority with groups of foliage-leaves. + +The flowers are without perianth. The male flower is sometimes an enormous collection of stamens (Fig. 258), which are flat in section; but in *Cycas* and *Zamiopsis* (Zamiopsis, *Ceratostoma*) like the sporophylls in Horsetail (Fig. 259); but in all, the pollen-sacs are situated in large and varying numbers on the back of the stamens, and are surrounded by the sporangia of the sort of Ferns (Fig. 241 b, c). On germination the micro- +Fig. 257.—Cycas circinata. + +**Fig. 257.—Cycas circinata.** +A leaf with circinate vernation. + +**Fig. 258.—Female cone of *Cycas circinata*.** +Male cones of *Cycas circinata*. Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +spore contains a bicellular anthocarpium in the upper end of the pollen-tube, the vegetative nucleus being found near its lower end. The inner of these two cells is the anthocarpial cell; this divides and forms two spermatia, with cilia at the anterior extremity, which move about within the tube, and finally penetrate the antheridium. Female flowers are wanting in *Cycas*, because the carpels do not terminate the apical growth of the stem. After a group of foliage- and scale-leaves, a group of carpels is developed, which pinnae are formed by the foliage-leaves, bearing on their edges a number of ovules (most fre- +Fig. 259.—Female cone of *Zamiopsis*. + +**Fig. 259.—Female cone of *Zamiopsis* (Zamiopsis, *Ceratostoma*).** +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 260.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 261.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 262.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 263.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 264.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 265.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 266.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 267.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 268.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 269.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 270.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 271.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 272.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 273.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 274.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 275.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 276.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 277.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 278.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 279.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 280.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 281.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 282.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 283.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 284.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 285.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 286.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 287.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 288.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 289.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 290.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 291.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size. The male cones are very numerous. + +**Fig. 292.—Male cone of *Zamiopsis*.* +Leaf 1-4 mm. +nat. size + +254 + +GYMNOSPERME. + +quently 5-6) (Figs. 245, 250); the same stem produces successively scale-leaves, foliage-leaves, and carpellae. The differentiation is not much more advanced than in certain Ferns (Schefflera, Blechnum), whose bare and fertile stems of different forms regularly alternate. The fertile stem has no leaves, but the carpellae are shield-like with Zonaria and Cortonaria (Fig. 240), and collected into conical flowers, which terminate the growth of the stem (Fig. 250). The number of ovules in these instances is two to ten. + +The seeds are large (most frequently 2-3 centimeters long) and plum-like; the external layer of the testa is fluffy, while the internal one is hard and horny. There are two systems of vascular bundles in the seed-coat, one for the embryo and one for the food. The embryo is straight, attached to the end of the suspensor, which is often long, filamentous, and rolled up; it has one or two cotyledons. + +The embryo in Cortonaria and others is very slightly developed, at the time when the seed germinates, but it grows rapidly after that, so that its further development and germination proceed. This calls to mind the Cycadopsidae, especially Selaginella, whose macroprosop are thrown off filiform with coleoptiles, while in Cortonaria they remain on the plant until the macroprosop from the parent-plant, while in the Cycadeen fertilisation is effected before the separation. In Cyanea the tests may rupture, and the zygospore grow out of them; but in Cortonaria the zygospore does not break through. This also is an indication of the prothallial nature. + +Gymnosperms are present in all organs. Collateral vascular bundles, with spiral and reticulate veins, are found in all organs. The vascular bundles take place by means of a cambium. An exceptional mode of growth is found in Cyanea and Eucalyptus; the latter has a peculiar leaf structure. The leaves are very small and new ones always arise in the central parenchyma just outside the bud, and which form a new ring of xylem and phloem. This may be repeated so that a number of leaves can be produced from a single bud. The leaves are erect or erecting; bolling calyx extends from the roots in a vertical direction and appears on the surface of the soil; these are prelmin leaves, in which a symphylous Alpin (Alopecurus) is found. + +The Cycadeen were formerly (from the Cretaceous to the Tertiary Cretaceous) far more numerous than at the present day. They appear to have been most numerous during the Tertiary period. Many species which have persisted to the present time are found in all tropical regions. Cyanea (Trop., and Sub-trop., Emirati Hamptons); Diosma (Mexico); Marocarne (Australia); *Cycas* (Australia); *Cycas* (East Africa); *Eucalyptus* (Trop., Australia); *Cortonaria* (Mexico), New Guinea, Western Australia; *Zizyphus* (Trop., Australia). + +Usta is made from the starch-containing pith of Cyanea revoluta and cirindica. The leaves are often used at meals and church festivals, under the name of "palm-brushes." + +**CONIFERAE.** + +**Class 2. Coniferae (Pine-trees).** + +The stem branches freely. The leaves are entire, relatively small, linear or reduced to scales. The flowers are without peri- +anth. The ovules naked. It is seldom that the female flower is reduced to a scale. + +Whilst the Cycadeae principally resemble the Ferns, the Conifers partly resemble the Lycopods, and partly the Equisetums—the former especially in the *nodicule* or scale-like, leathery, simple, and often persistent leaf—while the latter resemble the *sporophylla* of pines and oaks (Fig. 203, 270, 272). Ginkgo deviates from this, being no doubt the oldest, and the Conifer which stands nearest to the Cycadeae (Fig. 205). The resemblance to the Equisetums is especially owing to the fact that the female remains abundantly, and often in great numbers, forming pyramidal or conical branches. In addition to the foliage-leaves, scale-leaves (bud-scale) are present in the majority of species. + +The flowers are monocarpous or rarely dioecious. Perianth is wanting. The leaves are of the cotyledon-like male flowers (Fig. 207, J) are of different forms, but as a rule more or less shield-like. +As in the Cycadeae, the pollen-sacs are in all cases situated on the underside. There are, as a rule, two pollen-sacs (the Abietes, Fig. 206 A), and one or two (the Taxus, Fig. 206 B), a few have more, e.g. *Araucaria* (Fig. 242); they differ by clefts. + +If, in commencing our consideration of the female flower, we begin with that of Ginkgo, we shall observe in its corona of a scale- +like foliage-leaf (Fig. 205 C), a bud-scale (Fig. 205 D), each bearing one ovule, and reduced almost to the ovule itself (Fig. 205 C, D). The flower in *Podocarpus* is still further reduced, viz. to a single carpel with one ovule, which is anatropous and has two in- +tergenital bracts (Fig. 208 A). In *Pinus* there is a two-ovule-cake (see +in Fig. 208 D), and several female flowers of this kind may be col- +lected in a small anil cone, the stalk and bracts of which become fleshy +(Fig. 208 C). The external integument also becomes fleshy (an uii, +Duryalea), which is not so evident in *Pinus*. In *Cedrus*, the external +integument develops more independently as a finely aril +(Fig. 208 B, B'). Microcorysche also is clearly allied to these; +the bracts are more fleshy, and the ovule (i.e. female flower) +is protruded beyond the bract (Fig. 208 A'). Twoar scales +in a small scale-cake are present; but what has been reduced to an ovule is situated, in this instance, on the apex of a secondary +w. ii. + +255 + +256 +CYNOPPERME. + +branch which is studded with floral-leaves (Figs. 203, 204); an external integument is developed on all sides and surrounds the seed as a scarlet aril. According to this conception the aril corresponds to an external integument, and the Tocoidae thus possess a partly dichlamydeous ovary. Only Ginkgo and Cycadoleteus appear to deviate from this rule. The outer integument of Ginkgo (called the small outgrowth indicated by ar.) in Fig. 200 D, really is a radiculary, external integument; in Cycadoleteus, to which Ginkgo is most closely related, there is likewise only one integument. But in these two plants the inner integument is very thin and the seed resembles a drupe; while the Cycadoleteus there is an external fleshy covering and an internal hard one, and these two layers may probably be considered homologous with the two integuments. This theory is supported by the presence of vascular bundles in Cephalotaceae and Podocarpaceae, which present the xylem in the fleshly external layer to the outside of the testa, which is therefore the upper side of the integument (Cekhovskoy). + +The cover-scales are produced into scales only in Ginkgo and Torreya, more prominently in Podocarpaceae, but strongly in Cephalotaceae and Ginkgo. Cekhovskoy terms these ovules "holochlamydeous." + +If we pass from those to the order Pinaceae, we find the female flowers collected into catkin-like ones, which have been considered from various points of view to be sometimes single flowers, at other times compound inflorescences. The structure in *Astraceae* is as follows: first of all spirally arranged, scale-like leaves, covered with hairs (Fig. 207, 208), then a central axis, in the axil of each cover-scale a larger leaf-like projection, the *callophore scale*, is borne, which turns the upper side towards its cover-scale (which is shown by the fact that the wood of its vascular bundles runs from the cover-scale towards the callophore bundle of the cover-scale; Fig. 209). Two ovaries, with microspores directed towards the central axis, and with apparently only one integument (Fig. 205), are produced on both sides of each oviforous scale; i.e., each scale turned away from the central axis. The oviforous scales grow after fertilisation into the woody or leathery "cone-scales," which are usually much larger than the cover-scales. This ovary is therefore a dwarf-branch which is situated in the axil of the cover-scale, and bears two ovalets (in the same way as in Ginkgo, one long-stalked flower, reduced to two ovalets, is situated + +CONIFER. +257 + +in the axil of a leaf), and in this case the external integument of the ovule is expanded into leaf-like bodies, which have united to form one "sympodium" (equaliforma scale) which is inverted so that its dorsal side is turned upwards and bears the nucellus and the embryo-sac, while the ventral side is directed downwards. The carpell itself is therefore in this instance extremely reduced. In Picea (Fig. 268 B), which is found in several genera, represents then a third carpell, which is sterile. In the other orders of the Coniferae, the integument of the ovules grows together and finally forms a structure, which also is termed a "cone-scale", although from its development it cannot be homologous with the cone-scales of the Ablatocae. This connation is found in the genus Abies (Axelrod) and may be seen on the upper surface of the "cone-scale" by the presence of a stronger or alpine ridge or pad, the free portion of the ovular scale (Figs. 250, 255, 269). It is most strongly pronounced in Abies grandis (Fig. 269), but is absent on single structure, the cone-scale (Fig. 274). The vascular bundles in the under portion corresponding to the cover-scale, have the xylem towards the upper side as usual in leaves, whilst the bundles present in the upper side of the cone-scale, which thus represents the vegetative structure of the flower, are arranged in a hemi- +chlamydean ovule are then situated on the upper side of this cone-scale. According to this theory the CUPREAE appear to be the youngest type, a view which corresponds with their vegetative structure (Fig. 265). In Abies grandis (Fig. 269) and Abies amarans, then the flower is reduced to a single carpell and one ovule, as in the case of Diuracarpus and Microcarpus. If two or more ovules are present, then the same number of carpell may be present as well as one or more scales, but their ovules being developed into leaf-like structures which collaterally coalesce to form a "sympodium", or are suppressed. + +According to this theory, which is based on the researches of Goltzovsky, the female flowers of the Coniferae may be classed thus: + +1. In all cases situated in the axil of a bract and collected into cones, with numerous flowers or with few or one flower. In Ginkgo only one flower is present in each cone. +2. It is only in Taxus that bracteoles are present. +3. They are formed only from rudimentary carpels, in which the stem takes no part. + +258 + +**GIMNOSEPERME** + +4. The number of carpels in each flower varies from one to many, most frequently three, of which the central one remains sterile. + +5. Each carpel bears, only one ovule. The flower which is formed of only one carpel appears to consist of only one ovule. + +6. The ovule has in Taxaceae either a double integument (Podocarpus, Taxus), of which the external is the "aril," or, as in the Cycadeen, a single one, which is homologous with the two united together in the Pinales. + +7. The external integument in the Pinoidae is expanded to form a leaf-like structure—the ovuliferous scale—and bears on its dorsal side the ovules, which are thus only provided with one, and that the inner, integument. + +This later interpretation of the female cone in the Coniferae is more probably correct than the older one; that, however, which appeared in the former issues of this book may also be stated. It was to the effect that each catkin-like female cone consisted of two parts, namely, a staminate and a pistillate cone; both cones were single leaves, namely samarae, which bore the ovules on the sides which is turned upwards; the division into two parts which makes its appearance in the older scheme is due to a misunderstanding. In reality, the female cone consists with the division of a leaf into a bract and a fertile portion, which is found especially in Ophioglossaceae and Marattiaee, and with the liquid in Zoster. + +**POLLENATION** is accomplished by means of the wind. At the period of pollination the leaves are always so widely separated from one another, that the ovule can catch the pollen-grains carried to them by the wind; this is often effected by the mucilaginous drops which appear at the microsporangium and by the evaporation of which the pollen-grains are brought in contact with the nectary. Thus, when fertilisation has taken place, and the cones close together so that the seeds while maturing are enclosed, and it is not possible for them to fall out until they have been dispersed; these cones again become separated. In the Pinoidae, the fully developed ovuliferous scales are hard and woody; and in this condition the collection of female flowers is termed a cone. In the Taxoideae, true cones are an exception. 2-15 conelike structures are arranged in a whorl. + +The characteristic feature of this class is the abundance of resin, which is to be found in isolated cells (especially in the + +A diagram showing a pine cone with multiple cones attached to a central axis. + +**CONIFERAE.** + +259 + +cortex), partly in intercellular glands or passages (both in the cortex and wood). *Taxus* is the only genus which has no resin. + +There are about 850 species, mostly from the Northern Temperate zone (especially North America and Siberia), where they grow gregariously and form the most northern forests. The Juniper, Scotch Fir, and Yew are natives of Great Britain. + +This class may be divided into two families : + +1. **Taxodiaceae.** The ovules have either one integument, the external part of which is fleshy, and the internal hard and stone-like; or two integuments, of which the external is the fleshy and coloured "aril." "Ovuliferous scales" are wanting. The cones are usually small, irregularly scented, the bracts become fleshy, or come usually are not developed. The seeds project more or less freely beyond the bracts. + +2. **Pinoidaceae.** The ovules have two integuments, the external one of which is fleshy, and the internal hard and stone-like. "Ovuliferous scale," if there are several of these in each flower they unite and form a "sympodium." This may remain free or unite with the bract. The cones are most frequently woody, rarely succulent. The seeds are hidden among the cone-scales. + +Family I. **Taxodiaceae.** + +This family, considered to be most nearly related to the Cycadees, also made its appearance at a very early period. There is only one order in this family. + +Order. **Taxaceae.** The characters have been given above. + +A. **Cephalotaxus** is the oldest group, presumably the connecting link between the Cycadees and the other Conifers. The flower consists essentially of two parts : a male and a female. One integument. Seeds dropperous -The flowers in *Ginkgo biloba* (Ginko) are situated in the axils of foliage- or scale-leaves. The stamens bear only two pollen-sacs (Fig. 260 A). The female flower has two scales, placed opposite each other on a long bare axis (Fig. 260 D). Amongst the base of the ovule a small scale is found (Fig. 260 D) is found, which may probably be considered homologous with the collar-like outgrowth which surrounds the base of the Cycadees (Fig. 260 B). The seed is enclosed in a thin external coat, surrounding a hard internal layer. The embryo is developed after the seed has fallen off. The Ginkgo-tree has long-stalked, fan-shaped leaves, more or less indented, with dichotomous veins + +250 + +GYNOSPERM. + +resembling certain Ferns—the Elatineae. It is a native of East Asia, and the only surviving species of a genus which in earlier times was very rich in species, and distributed over the entire Northern Hemisphere. *Cephalotaxus* (Eastern Asia) is related to it. +II. *Podocarpus*. The female flower is reduced to one ovule, placed in the axil of a bract, or a little forward upon it. The ovule has an aril (2 integuments)—*Phyllocladus* (New Zealand). In New Zealand, this plant, has obtained its name from its flat, leaf-like branches, the leaves proper being scale-like (*Jf*). + +The ovules stand erect in the axil of the short branches, and the seeds are collected at the end of short branches. +*Microcarpus tetrapoma* (Tasmania) has a small, fleshy aril with several spines, placed, flimsy branches, on which the inward and downward turned ovule is attached (Fig. 262 A, A'). The ripe cones average about 3 inches long—*Araucaria*—berries—in *Dacrydium* (Tasmania, New Zealand, Malaysia) the female cone has most frequently only 1-2 (-6) bracts, which re- + + +A branch with a small flowering dwarf-brach (male flower); & a male Cnidospora (female flower). + + + +Female flower of Podocarpus. + + + +Female flower of Podocarpus. + + + +Female flower of Podocarpus. + + + +Female flower of Podocarpus. + + +CONIFERAE. +201 + +seem like the vegetative leaves; they have also a fleshy aril (Fig. 202 B, D)---Podocarpus (40 species, East Asia, S. Temp.); the bracts of the female flowers become fleshy, and unite together; only 1 or 2 are of use in supporting the flowers. The ovules + +A simple carpel with its ovule. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. +A branch with female flower. + +Fig. 202.--Microcarpus: *female* cone (I). A simple carpel, with its ovule. E. *Eucalyptus*: a branch with *female* flowers. If This flowers; or the bract; at the side; or, rarely, on the top of the *female* shower with 6 ovules. D *Larrea* *brevifolia*: shower, from 1 ovule. + +project high above the apex of the bract, and are anatropous, the micropyle being turned downwards (Fig. 202 C, D). An aril commonly surrounds the ovule, which is an external coating, and later on it becomes fleshy and coloured. + +C. *Taxus*. The *female* flower is reduced to one ovule, which is situated terminally on an axis which bears 2-3 pairs of opposite, scale-like leaves. In consequence the Taxaceae form a very isolated group among the Coniferæ. + +*Taxus* (*T. baccata*, the Yew-tree). + +Dioecious. The *female* flower consists of a single ovule at the end of a short secondary branch (Fig. 204), which is studded with scale-like leaves. The aril when ripe is fleshy; sometimes yellowish and only loosely envelopes the seed (Fig. 203). The leaves are scattered, flat, linear, and pointed (Fig. 205). + +Fig. 203.--Female branches: brachy +with two ripe seeds (Gmelin). + +262 + +GYMNOSPERME. +(264). The short male flowers have 5-8 pollen-sacs, pendent from the stamens, and are surrounded at their bases by scale-like bracteoles (Fig. 243). *Torreya* (4 species, N. America and Japan) is closely allied to *Taxus*. The style ultimately fuses with the woody inner integument, and hence the ovule becomes drupaceous, as in Cephalotaxus. + +A detailed botanical illustration showing the structure of a female flower of *Taxus baccata*, including the ovary, style, and stigma. +A detailed botanical illustration showing the structure of a male flower of *Taxus baccata*, including the stamens and pollen sacs. + +Fig. 243.—*Taxus baccata*: A shoot of *Taxus* with female flowers at the base when the ovary is still green; and a similar shoot with mature female flowers. Longitudinal median section through a female shoot; a growing point of primary shoot; a commen- +ment of cotyledonary leaf.
+Ussn.: *Taxus baccata* is usually planted in gardens, especially in hedges. Its wood is very hard and is used for wood-carving. The shoots are poisonous, +but not the aril, which is often eaten by children and by birds. + +Family 2. *Pinoidem*. + +The four orders differ from one another partly in the arrange- +ment of the leaves (Cupressaceae have opposite or verticillately + +**CONIFERAE.** 263 + +placed leaves, flowers, and inflorescences ; in the others they are placed spirally), but chiefly in the greater or less degree of union which takes place between the female flower (the leaf-like "sym- +phyllodium") and its supporting cover-scale, and in the position of the ovules (the megaspore being turned upwards or downwards). + +The e-ovulate scale is represented by the "cover-scale" alone, in the others by their union with the cover-scale. + +Order 1. *Araucariaceae.* This order most frequently has solitary ovules, turned downwards and attached to the centre of the conical scale (Fig. 250). In *Araucaria* (Dacrydium) the ovule is the most simple, a winged seed (Fig. 265), which hangs freely downwards, being borne in the centre of the undivided one-scale. In *Arau- +caria*, the stamens with the free, pendulous pollen-sacs have been represented in Fig. 262; the ovuliferous scale is united for nearly + + +Description: A diagram showing the structure of a plant's reproductive organs. + + +Figs. 250.—Apatites (Araucaria) australe. Cross-section with the seed. A longitudinal section.—A, from within; b, f, n, n', n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n", n". The figure shows a cross-section of a plant's reproductive organs, including the seed and various parts of the plant. + + +its whole length with the branch, and projects from apex to apex in the shape of a triangle, its base, scale, resembling the ligule in *Lecodea*, and may therefore be termed a "ligule." *Araucaria* (S. America, Australia) has often rather broad leaves (*A. brasiliensis*). The ovuliferous scale in *Cunninghamia* is more distinct, and stretched out beyond the entire cover-scale; it bears three inverted ovals (Fig. 265); (from New Zealand). + +Dammaraeus, which is used for varnish, is obtained from *Apatites* +(*Dammara* species (New Zealand, Philippine Islands)). + +Order 2. *Abietaceae* (Pine and Fir Trees). The leaves are spirally arranged and needle-like. The flowers are monocious. + +263 + +254 +GENOPOEEMA. + +The male flowers are long, and catkin-like, with numerous stamens, each bearing two along pollen-sacs. +The pollen-grains are most frequently tri-bladed, having two blader-like appendages, formed as outgrowths of the expanse, to assist in their distribution by the wind (Fig. 207 A-D). The upper appendage is usually longer than the lower, but this relation between the erect and the ovuliferous scale, which is found in the preceding order, is not in this instance so complete; these scales make their appearance as two free parts, and are attached only at their bases (Fig. 208); the lower portion is the cover-scale, in which, in the male reed-pine (Pirin, Pipturus, and others), it is only in the "Noble Pine" (Abies) and Pseudotsuga douglasii, that it attains a greater length than the ovuliferous scale (Fig. 207 B-G). On the other hand, the upper part, the "pollen-sac," being attached to the cover-scale (the inner side turned upwards), grows strongly and elongates, especially after fertilisation, becoming woody or leathery; it is commonly termed the "cone-scale," but is in reality only homologous with a part of + +A-D. Pseudotsuga douglasii. A cone. B cone-scale, with the inner side turned forward; the points of the over-scale are seen behind it. C-D transitions from the ovuliferous scale to the pollen-sac. E-F. Abies nobilis. E cone-scale; F pollen-sac. G-Picea excelsa. G cone-scale; H pollen-sac. + +A D E F G H I J K L M N O P + +Fig. 207.—A-D. Pseudotsuga douglasii. A cone. B cone-scale, with the inner side turned forward; the points of the over-scale are seen behind it. C-D transitions from the ovuliferous scale to the pollen-sac. E-F. Abies nobilis. E cone-scale; F pollen-sac. G-Picea excelsa. G cone-scale; H pollen-sac. + +G H I J K L M N O P + +**CONIFERAE.** 265 + +the "cone-scale" in the other order of Pinaceae. On the side of the ovuliferous scale, turned towards the axis, are situated two ouvles with microspores directed inward. The seeds are most frequently provided with a false wing (a tissue-like part of the surface of the ovuliferous scale). Cotyledons, more than 2, certifiably occur in some species, but they do not seem to offer pollination. In Picea, for instance, the pollen-tube only penetrates the nucellus for a short distance during the year of pollination, and then ceases its further growth, fertilisation not taking place until after the middle of the next year; whilst the seeds ripen about a + +A diagram showing the structure of a cone-scale. +Fig. 301.--A. Aline: c the cover-scale; e the cone-scale; f, "conescale," &c., ovules in a young fruit; g, the nucellus; h, the seed; i, the embryo; j, the endosperm; k, the covered microspore; l, m, n, o, p, q, r, s, t, u, v, w, x, y, z, the cover-scales behind. +B. Aline: ripe "conescale" with two ovules. + +year and half after pollination. In the Larch and others, the seeds are mature in the autumn preceding pollination. + +*Alire* (Fir). The leaves are often (e.g. *Abies perniciosa*) displaced into 2 rows, flat and imbricated at the apex, with 2 white (wax-covered) scales on the upper side of which the stomata are situated. The leaf-scales are nearly circular and do not overlap. The cones are erect. The cover-scale and the ovuliferous scales separate from the axis, to which they remain attached in other genera.--*Picea* (Pine). The leaves are usually imbricated and have persistent scales. When they are so disposed that they form a transition to *Picea*, *Pinus*, but the cover-scales grow out of all proportion to their size (e.g. *Pinus contorta*), *Pinus* is considered as sub-genus of *Alire*.--*Picea*. The leaves project on all sides, square and pointed; the leaf-scars are + +206 +GYMNOSPERME. +rhombic, or projecting leaf-cushions. The cones are pendulous. +The cover-scales are much shorter than the leathery, persisting ovuliferous scales. --The genus *Larix* (Larch) differs from all the others in having deciduous leaves (the three preceding have leaves which persist for eleven to twelve years). It has long-branching dwarf-branches, which each year form a new rosette of foliage-leaves, similar to those on the long-branches. The male flowers and the erect cones resemble those of *Picea*, and are borne on dwarf-branches, but the female cones are sessile, and are very small, but has persistent leaves (*C. libera, C. decalvus*--Pine) (Pinus) has long-branches and dwarf-branches. The leaves of the long-branches are scale-like and not green; the dwarf-branches have very little foliage-leaves, and last one year only; they arise in the axils of the scales borne on the long-branches of the selfsame year, and each bears 2–5 foliage-leaves; they are also surrounded at the base by a number of membranous bud-scales. The cone-scales have a thick, rhomboid cutiniferous (the "shoed")". + +The buds which develop into long-branches arise in the axles of other long-branches, and remain there until they become fully developed; they occupy the position of long-branches, and take about two years for their development. The male flowers arise close together, and form a spike-like inflorescence at the base of the long-branch; this spike is often so large as to occupy the position of dwarf-branch, so that a female cone may be considered to be a modified long-branch, and a male a modified dwarf-branch. The main axis of the long-branch is called the *crown*; it is formed by the union of the outer parts, and on dwarf-branches it is not until some time later that the dwarf-branches are developed and their permanent arrangement attained. + +These trees grow in forests, especially in mountainous country, partly on leathery and mossy, and partly in plantations as an ornamental tree, such as *Mackenzia* (Mackenzia), *Picea* (Pine), *Abies* (Fir), *Larix* (Larch); Eur.; Scotch Fir (f. alterata); Eur.; Weymouth Pine (f. scotica; N. Am.); common Red Pine (Pinus sylvestris; N. Am.); White Pine (Pinus strobus; N. Am.); alpine Fir (Abies alpina; N. Am.). The genus *Abies* (Fir) includes several species (Crinum, Canouanis) ; *A. balsamea* (N. Am.) ; *Tengk canadensis* (N. Am.) ; *Paradendron douglasii* (W.S. Am.) ; Larch (Larix canadensis; Alp.; Carpathian); *A. olitica* (N. Am.) ; *A. excelsa* (N. Am.) ; *A. grandis* (N. Am.) ; *A. rubens* (N. Am.) ; *A. pungens* (N. Am.) ; *A. sibirica* (N. Am.) ; *A. vestita* (N. Am.) ; *A. glauca* (N. Am.) ; *A. crenata* (N. Am.) ; *A. amabilis* (N. Am.) ; *A. papyrifera* (N. Am.) ; *A. alba* (N. Am.) ; *A. excelsa* (N. Am.) ; *A. grandis* (N. Am.) ; *A. rubens* (N. Am.) ; *A. pungens* (N. Am.) ; *A. sibirica* (N. Am.) ; *A. vestita* (N. Am.) ; *A. glauca* (N. Am.) ; *A. crenata* (N. Am.) ; *A. amabilis* (N. Am.) ; *A. papyrifera* (N. Am.) ; *A. alba* (N. Am.). The wood of these trees is very hard and in use for heavy work; it is used with essential oils, the name being derived from the Terebinth-tree, from which formerly a medicinal material was obtained are extracted from Pines furicaceae and Picea ols; it is also used for making oil from pine seeds with water; Tar by dry distillation of Fine-wood, Canada-balsam is from North + +**CONIFERAE.** 207 + +American alder-species (i. e. *Alnus* and *Fraxinus*). The official Turpentine is mainly obtained from *Pinus pumila* (South of France), *P. sylvestris*, *austriaca*, *crocea* (Venetian Pine), and other North American species; more recently also from *Pinus strobus* (White Pine) and *P. resinosa* (Red Pine); the latter, Venetian Turpentine, from Larch (S. Eur.). Amber is resin from a Tertiary plant (*Pityrogramma succinifera*), closely related to the Pine, which grew especially in the Eocene epoch, and was found in the Eocene deposits of the Alps (the Foss. S. Eur.) has edible seeds and also *F. cembra* (in Cen. Eur. and Siberia). + +Order 3. **Taxodiaceae.** The vegetative leaves and cone-acules are arranged spirally. The ovules (2–9) are situated either at the base of the ornithocarpic scales, or on the sides, when they are erect; or at their centre, when they are generally more or less inverted. The ovuliferous scale is more or less united with the perianth, and projects beyond the surface of the cone-leafs like a comb (Fig. 209). The vascular bundles, which extend into the cover-scale, have the usual horizontal course, but the vascular bundles enter the ovuliferous scale; the xylem is placed towards the base; while those bundles which enter the ovuliferous scale have this arrangement of the bundles reversed. + +Taxodium distichum (the North American "Swamp Cypress") has annual leaf-buds, and is a deciduous tree. In the Tertiary period it was very common in the Polar regions. Sequoiadendron giganteum is the famous Californian Giant-Fir, or Mammut-Tree, which attains a height of 150 feet and a girth of 18 feet. It flourishes from 6000 to 14,000 years. *Cycas revoluta* (Japan, China) has the least adnate ovuliferous scale; *Ginkgo biloba* (China); *Atherosperma* (Tunania); *Schizogyne cordifolia* (the only known species of this genus); *Cupressus macrocarpa* (California), in which those which are situated at the apex of the annual shoots support "double needles"; i.e., dwarf-branches similar to the two-leaved dwarf-branches of *Cupressus sempervirens*. The leaves are opposite or verticillate, sometimes acicular, but most frequently scale-like (Fig. 210). These plants are species with leafy leaves; but in some instances often commence with a bud-scale (Fig. 211), and branches are sometimes found on old plants which revert to this form, seeming to indicate that the acicular leaf was the ori- + +Fig. 209.—Taxodiaceae: Juss. +Portion of longitudinal section through cone, +showing arrangement of vascular bundles in +ovuliferous scale. +207 + +208 + +Gymnosperm. + +ginal form (stamens). The so-called "Reticulata" species are seedling-forms of *Bistia*, *Thuja*, *Chamaecyparis*, which have been propagated by cuttings, and retain the seedling-form. The flowers are monococious or dioecious. The male flowers are short, and have shield-like stamens, bearing most frequently several pollinum. The female flowers are large, and consist of a single cone together and form undivided cone-scale, opposite or whorled; the **coniferae** scales have slight projections near the base on which 1–2–several erect scales are developed (Fig. 274). Most frequently 2 cycloids.—Cycas trees and shrubs. + + +A branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch of a branch. + + + +Portion of the cone-scale (Fig. 275). + + + +Section through the cone-scale (Fig. 276). + + + +Section through the cone-scale (Fig. 277). + + + +Section through the cone-scale (Fig. 278). + + + +Section through the cone-scale (Fig. 279). + + + +Section through the cone-scale (Fig. 280). + + + +Section through the cone-scale (Fig. 281). + + + +Section through the cone-scale (Fig. 282). + + + +Section through the cone-scale (Fig. 283). + + + +Section through the cone-scale (Fig. 284). + + + +Section through the cone-scale (Fig. 285). + + + +Section through the cone-scale (Fig. 286). + + + +Section through the cone-scale (Fig. 287). + + + +Section through the cone-scale (Fig. 288). + + + +Section through the cone-scale (Fig. 289). + + + +Section through the cone-scale (Fig. 290). + + + +Section through the cone-scale (Fig. 291). + + + +Section through the cone-scale (Fig. 292). + + + +Section through the cone-scale (Fig. 293). + + + +Section through the cone-scale (Fig. 294). + + + +Section through the cone-scale (Fig. 295). + + + +Section through the cone-scale (Fig. 296). + + + +Section through the cone-scale (Fig. 297). + + + +Section through the cone-scale (Fig. 298). + + + +Section through the cone-scale (Fig. 299). + + + +Section through the cone-scale (Fig. 300). + + + +Section through the cone-scale (Fig. 301). + + + +Section through the cone-scale (Fig. 302). + + + +Section through the cone-scale (Fig. 303). + + + +Section through the cone-scale (Fig. 304). + + + +Section through the cone-scale (Fig. 305). + + + +Section through the cone-scale (Fig. 306). + + + +Section through the cone-scale (Fig. 307). + + + +Section through the cone-scale (Fig. 308). + + + +Section through the cone-scale (Fig. 309). + + + +Section through the cone-scale (Fig. 310). + + + +Section through the cone-scale (Fig. 311). + + + +Section through the cone-scale (Fig. 312). + + + +Section through the cone-scale (Fig. 313). + + + +Section through the cone-scale (Fig. 314). + + + +Section through the cone-scale (Fig. 315). + + + +Section through the cone-scale (Fig. 316). + + + +Section through the cone-scale (Fig. 317). + + + +Section through the cone-scale (Fig. 318). + + + +Section through the cone-scale (Fig. 319). + + + +Section through the cone-scale (Fig. 320). + + + +Section through the cone-scale (Fig. 321). + + + +Section through the cone-scale (Fig. 322). + + + +Section through the cone-scale (Fig. 323). + + + +Section through the cone-scale (Fig. 324). + + + +Section through the cone-scale (Fig. 325). + + + +Section through the cone-scale (Fig. 326). + + + +Section through the cone-scale (Fig. 327). + + + +Section through the cone-scale (Fig. 328). + + + +Section through the cone-scale (Fig. 329). + + + +Section through the cone-scale (Fig. 330). + + + +Section through the cone-scale (Fig. 331). + + + +Section through the cone-scale (Fig. 332). + + + +Section through the cone-scale (Fig. 333). + + + +Section through the cone-scale (Fig. 334). + + +**CONIFERE.** 303 + +Monosoma. Cones oblong. The cone-scales are dry, as in the Cyprinus, but leathery and imbricate, and not shield-like; each cone-scale bears 2-5 seeds. The leaves are most frequently dimorphic; those leaves which are situated on the edges of the flat branches are compressed, and only these bear buds, which are arranged in a spiral manner (Fig. 271). The leaves on both sides of the branch; those which are situated on the flattened surfaces are pressed flat and broad, and never bear branches (Fig. 271). +Along the central line of each leaf there is a resin- +canal (Fig. 271) - *Chamaespargus*, *Cultivis*, *Lobanacra*, *Tropisus* (species : 2, obsolete; in Japan). + +A diagram showing the structure of a conifer cone with a focus on the central line of each leaf. +Fig. 271.—Branch of Juniper with "berry-cone." + +**OFFICIAL.** +Juniperus sabina from Central Europe and North Africa of Europe (the young twigs yield an essential oil), the wood of *Cupressus* in the production of an essential oil, and *Cypresses* in the production of empy- +rerial oil, and *Thuja occidentalis* in the production of oil used for gin. The wood of *Rutidium* (N. Am.) is known as red cedar, and is used for lead-pencil. Sandaracop gum is obtained from *Cultivis quadrifolia* (N. W., E.). The following are cultivated in gardens—*Thuja occidentalis* (Aubert vitis) (N. Am.), and *orientalis* (China, Japan); *Juniperus sabina* and *repinicola* (Europe); *Juniperus sabina* and *repinicola* (S. Eur., W. Asia), and other species, are grown especially in conservatories, and in Southern Europe particularly in ornamentary.—The Betulina species which are cultivated in gardens are: *Betula alba*, *Betula pendula*, all are obtained from cuttings, taken from seedling-plants with sterile leaves (see page 207). + +An illustration of a juniper branch with a berry-cone. + +270 + +GYMNOSPERME. + +Class III. Gnetace. + +This class, independent of extinct forms, comprises the most highly developed of the Gymnosperms, partly from the circumstance that a perianth of 2-4 members encloses the *terminally* + +A botanical illustration showing a plant with a long, thin stem and a cluster of small leaves at the top. +Fig. 231. -- *Mikrolobium* *sphaerocarpum*. The terminal lamina indicates the number of the sepals. + +The perianth is represented by a single leaf-like structure. + +GYNECUM. 271 + +placid oval, which is provided with one, or (in Guttum) two, integuments and partly owing to the fact that the wood has true vessels. There is only one order. + +Order. Gymenaceae. The three known genera differ very much in appear- +ance. *Wolfeitchia mirabilis* (from the deserts of South Western Africa) is the +chief of these. It is a small tree, about 30 feet high, and its wood is peculiar; +it is the only part of the main axis of the stem which becomes developed. It +attains a circumference of upwards of four metres with a length of 3-4 ft. +of wood. The bark is smooth and greyish-brown. The leaves are long and thin, +segmented at the apex and lie on the surface of the soil; these are the two first +foliaceous leaves which succeed the cotyledon, and they are remarkable for their +covering of a large number of minute hairs. These hairs are so numerous in their +abundance as to give to the plant itself, in its soil axes situated the coved, spike- +like mass of hair which is seen in the picture. The perianth consists of two parts: the +perianthil is contained in one of it alternating pairs of leaves, the inner ones of which +are slightly united. The androecium likewise consists of 3 whorls: the external +(ventral) whorl consists of 6 stamens, each with a short filament; the second whorl of 6 +filaments uniting to form a cup. Each of the terminal anthers corresponds to a +series of 5 pores; the sporangia being fused together, and opening at the top +by one or more apertures. The ovary is composed of 3 free segments, or simple +ovules. In the $Q$ flower a perianth of two common leaves is present.--*Ephedra* +(desert plants, especially in the Mediterranean and W. Asia) at first sight re- +sembles *Wolfeitchia*, but differs in having its leaves opposite, small and united into a bidentate sheath; $2$ perianths of two common leaves +(median leaf); $3$ stamens united into a cup; each anther furnished with a short filament, +and each anther opening by a single pore. In *Ephedra* there are rare +rounded by the perianth which finally become red and hairy. There are 30 +species in this genus, distributed over all warm countries except Australia. + +They are mostly climatic (Liamas) from Tropical Asia and America. The $Q$ +flowers have a tubular perianth, formed from two median [leaves] which +narrowly enclose the ovary, and from two lateral leaves which surround it; this flower +has similar a perianth, surrounding an ovule provided with 2 integuments. + +The perianth becomes flimsy and envelopes the hard seed. 30 species. + +From this it appears that in both *Wolfeitchia* and *Ephedra*, besides +stamens, possess also a rudiment of an ovule. Culhavsky draws the inference that +the earliest Gymnosperms had homodimorphic flowers which from this structure became heterodimorphic; but he does not consider that this was the case for +*Wolfeitchia* only, in which this differentiation was only carried out in the $Q$ +flower. This theory has no far been scarcely proved. + +Fossil Gymnosperms. + +The earliest confirmed plants which are known belong to the Carboniferous, +a group of plants which lived during that period; they were Gymnosperms, +but it has not yet been determined whether they were Cycads or Coniferae. +The Cycads, even in the Coal period, were scarce; they obtained their +fules from seeds which were small and round; they were not very rich in species and genera, and extended as far as the Polar regions. In addition W. tI + +2 + +272 +GYMNOSPERM. +to these, Taxodium, Abietites, and Taxodiaceae appeared in the Carboniferous period. The Taxodiaceae appear to have attained their culmination in the Jurassic and Cretaceous periods; Ginkgo appears in the Rhetian; Torreya, in the Cretaceous; and Sequoiadendron, in the Tertiary. The genus Sequoiadendron also appears in the Carboniferous; Ficus was first known with certainty in the English Hith, but its presence in the Carboniferous is uncertain. Other genera are represented in this latter period. The Anacardiaceae first appear, very probably, in the Jurassic. The Taxodiaceae may be traced back as far as the Carboniferous (7th), but they became extinct during the Triassic period. During that period they spread throughout the entire Arctic zone, and being represented by a large number of species, formed an essential part of the forest vegetation. Sequoiadendron, a genus of the same family as Sequoia, is now known only by its fossil remains, first known with certainty in the Jurassic, but they appeared more frequently and numerously in the Tertiary period, in which most of the present living genera were to be found. In the Carboniferous period, two genera of the family Ficus were represented in the Coal period by the genus *Staphylinopspermum*, which had four ovate leaves. + +Recent investigations have established Ginkgophyceae as a distinct Class intermediate between the Cyanophyceae and the Coniferae. Ginkgo biloba being the only existing representative of this Order. It is more closely allied to the Gymnosperms. + +The pollen-grains are spherical, and in those a prolamella is formed generally composed of three cells, the outermost of which is the antheridium. This contains two ovules spermatocytes having at the anterior end a three-lobed spiral groove bearing numerous cells (Fig. 273a). + +Fig. 273a.—Ginkgo biloba. +Magnified view of one of the +pollen-grains. + +The pollen-grains are spherical, and in those a prolamella is formed generally composed of three cells, the outermost of which is the antheridium. This contains two ovules spermatocytes having at the anterior end a three-lobed spiral groove bearing numerous cells (Fig. 273a). + +DIVISION V. +ANGIOSPERMÆ. + +See pages 3 and 224. To this Division belong the majority of the Flowering - plants. They are divided into two parallel classes, the Monocotyledons and the Dicotyledons, which differ from each other not only in the number of cotyledons, which, with a few exceptions, is two in the former class, but also in many other points, such as the internal structure of the stem, the venation of the leaves, the number of the parts of the flower, etc. Assuming that these two classes are separate divisions, we may suppose that the Monocotyledon is the first, and amongst the Polyparvium in the second class that we might expect to find closely allied forms, which might reasonably be supposed to have varied less from their parent stock than those of the Monocotyledon, and yet be still distinct, without exhibiting any close relationship. It is easily proved that the Monocotyledon are the older class. + +(Only one genus is included under the Angiospermae which has recently been considerably increased by Trewn (Journ. d. Zool. Bot. de Berliner, 1891), who has shown that the Camarinae differ in many important points from the typical Angiospermae. Among other characters this pollen is found to cover the ovule near the chalazal end and thus at once distinguishes them from the Carpophyllum, and Trewn therefore suggests that these plants should be placed in a subdivision termed Chalazangamæ. + +According to this view the principal divisions of the Angio- +spermae would be represented thus: + +Angiospermae + +Sub-division. +Chalazangamæ. +Poridumæ. + +Class. +Chalazangamæ. +Monocotyledones, Dicotyledones. + +More recently Dr. Wahlen (Phil. Journ., ser. iii., xxv.) has shown that Bertia, and Miss Benson (Ferra. +Linn. Soc., 1894) that Alnus, Carpinus, and Carpinus also belong to the Chalazangamæ. + +A page from a botanical text book. +473 + +274 + +*Our knowledge, however, is still so incomplete that one would hesitate to accord the full systematic value which Dr. Trew attaches to his discovery until the limits of the Chasmatogamous group are better defined; and it would hardly be justifiable to include the Casuarinae and the above-noted genera in one family.* + +Class I. Monocotyledones. + +The embryo has only one cotyledon; the leaves are as a rule scattered, with parallel venation; the vascular bundles of the stem are closed, there is no pith, and the leaf-surface is typically constructed of five-nerved leaves, placed alternately. + +The embryo is generally small in proportion to the abundant endosperm (exception, see Helicopsis), and its single cotyledon is often almost entirely enclosed by the endosperm. In some cases, the seed either the entire cotyledon, or its apex only, most generally remains in the seed and absorbs the nutritive-tissue, while the lower portion elongates and pushes out the plumule and radicle, which thus proceed independently of each other. The primary root in most cases soon ceases to grow, but at this time it may recover numerous lateral roots break out from the stem, and become as vigorous as the primary root, or even more so. Increase in thickness of the stem is usually very slight; but there may be very little or not at all, and generally die after a shorter or shorter time. + +The stem is frequently a corn, bulb, or other variety of under-ground stem, as the majority of the Monocotyledons are perennial, herbaceous plants (see page 305). The stem is thickened (Fig. 270), and no cambium by which a continuous thickening may take place. The stem of the Palms, however, attains a very considerable thickness, which is due to the meristem of its growing-point continually increasing in diameter for a lengthened period (often for many years); but in this case also, when this condition the growing-point has the form of an inverted cone, and it is only when this cone has attained its requisite size that the formation of a vertical cylindrical stem commences. Certain trees like Liliopsida have a similar structure (see page 306) in their thickness; this is due to a meristematic layer, which arises in the cortex, outside the original vascular bundles, which were formed at the growing-point of the stem. This meristem continues to form thick-walled parenchyma and new, scattered vascular bundles. The primary vascular bundles, in the Palms and others, run in a + +A diagram showing a cross-section of a plant stem with a central pith and surrounding vascular bundles. + +**MOROCOTYLEDONES.** + +275 + +curved line from their entrance into the stem at the base of the leaf, towards the centre of the stem, and then bend outwards and proceed downwards in a direction more parallel to the sides of the stem (Fig. 277). The bundles formed later, in those stems which have thickened by the growth of the leaves, are similar. + +The branching as a rule is very slight, the axillary buds of the majority of the leaves never attaining development, e.g. in the Palma, buibous plants and others. As the cotyledon arises singly, + +A diagram showing the branching pattern of a plant with two rows of leaves. +Fig. 278.—Transverse section of the stem of a plant with two rows of leaves. +b-b the basal portion of the vascular tissue. + +the succeeding leaves also must be scattered, but they are frequently arranged in two rows (Grasses, Iris, etc.). The first leaf borne on a branch (the "Fore-leaf," i.e., the bracteole, if on a floral shoot) has generally, in the median plane, a characteristic form and position, being placed on the posterior side of the main shoot, and hence turned towards the main axis; it is sometimes provided with two laterally-placed keels (Figs. 279 f, 280 a), but the midrib is often absent. It arises in one piece from two primordia, which at this stage are distantly placed, and is usually described as formed by two leaves. It is, however, only one leaf, a fact which is evident from several circumstances, one being that it never supports more than one shoot, and this stands in the median phase (Fig. 279). + +The Fore-leaf is without stipules; its blade is usually long and without stipules; the blade is most frequently long, ligulate, or linear, erect, with parallel venation, the veins being straight or curved + +"Fore-leaf" is adopted as a translation of "Yerblatt." + +Fig. 277.—Diagrammatic representa- +tion of a branch with two rows of leaves, +showing the vascular bundles, from the stem into the leaves. + +276 + +**MONOCOTYLEDONOUS.** + +(Figs. 300, 301). Connecting the large number of veins which run longitudinally, there are as a rule only weak transverse ones. +It is very rarely that other forms of leaves are found, such as cor- +dates (Figs. 302, 312), or that the blade is branched, or the venu- +lation is forked (Fig. 303). The opposite is the case with the leaves; these deviations are especially found in the Araceae, the Palmae, the Scitamineae (Fig. 308), the Dioscoreaceae, and in several aquatic plants. The incisions in the Palm-leaf are derived by the split- +ting of one vein. + +The structure of the flower is generally as follows: P1=+3, +A3+3, G3, rarely S3+P3 with the other members unchanged.¹ +Instead of 5, the numbers 2 and 4 may occur; rarely others. In all these cases the petals are usually united into a tube. Alternate with one another, most frequently in the 3-merous flowers, as in the diagram (Fig. 278). This diagram is found in the following + + +Diagram of the ordinary, regular flower in the Monocotyledons: a is the bract. + + +**Fig. 278.—Diagram of Juncus: this bract is in its axil a shoot with its bractlets.** +**Fig. 279.—Diagram of Orchis: the lip: e or the two staminodes.** +**Fig. 280.—Diagram of Orchis: the lip: e or the two staminodes.** + +Orders: +Liliaceae, Convallariaceae, Juncaceae, Bromeliaceae, Ama- +ryllidaceae, Dioscoreaceae, Palmae, Araceae, and in some small orders, such as those considered as typical of the monocots, but also the starting point for the exceptional orders. The ovary in many Monocotyledons has many ovules, and their fruit becomes a many- +seeded berry or capsule; this form is no doubt the oldest. In others they have few ovules and their fruit becomes a berry. The fruit then becomes a cupule, or a drupe (e.g. Graminaceae, Cyperaceae, Palmar., etc.). + +Derivations from this typical floral structure in some instances + +¹ Regarding these and other abbreviations see the appendix in the book. + +MONOCOTYLEDONS. +277 + +may be traced to expression, very rarely to a splitting of certain members, the typical relative positions not being changed. Thus, the Iridaceae, the Cyperaceae, most of the Gramineae and some Juncaceae deviate in having only 3 stamens (Fig. 279), the inner whorl of which is usually wanting; but in the majority of these genera the stamens differ in the posterior stamen not being developed ; Zingiberaceae (Fig. 314), Marantaceae, and Casuarina, in the fact that only 1 of all the stamens bears an anther, and the others are either sup- pressed or reduced to mere filaments, or even to mere scales, perhaps cleft in addition. The Orchidaceae deviate in having, generally, only the anterior stamens of all the developed (Fig. 280). This is, in such instances, the suppression of certain parts of the flower; but it is not a complete suppression (as in the Hyacinth in one plane), chiefly in the inner perianth-whorl; but also in the other whorls. In the Orchids, the perianth-leaf (the labellum, Fig. 280 f) which is directly opposite the fertile stamen, is larger and more conspicuous than any other part of the flower; and this leaves may also be suppressed; see, for example, the two diagrams of the Cyperaceae (Fig. 284). In some orders the suppression of these leaves, which form the basis of the diagram, is so complete that it is hard to reduce them to any definite type. Thus, in the thre- eletiolous Liliaceae (Figs. 295) and Lemna (Fig. 303). +In the first family, which especially comprises water-plants, a some- what different structure is found; thus, Fig. 282 differs somewhat from the ordinary type by having only 3 stamens; but the floral diagram which occurs in this family may perhaps be con- sidered as the most probable representatives of an older type, from which the ordinary pentalacmoid forms have taken their origin. In favour of this theory we may point out that in some of these, the spiral arrangement of some of these in the flowers is large and indefinite number of stamens and carpels, the perfectly episcopalous gymnoecium which sometimes occurs, etc., etc. + +The Monocotyledons are divided into Families— + +1. **HELICOPHORAE.** This family forms a group complete in itself. It commences with Juncus, where there are only 3 stamens; then there is sporophore and ter- minates in epigynous and more or less reduced forms. +2. **ZINGIBERACEAE.** These have as a starting point the same diagram as the following families. +3. **BRADYCHILACEAE.** Also an independent branch, or perhaps two different ones which terminus in less reduced forms. +4. **EXANTHOMATACEAE.** These ought perhaps to be amalgamated with the follow- ing family. + +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. +A diagram showing a flower with three stamens. + +278 + +**MUCOSTOTILEXEOUS.** + +5. **LILIIFLORE.** These advance from forms with the typical diagram and hypogynous flower, to epigynous and reduced forms. + +6. **NARCISSOIDEAE.** The narcissus family. + +7. **GYRANZAE.** Two isolated families, which probably have taken their ori- +gin from Liliiflore, and have epigynous, mostly zygomorph, and much re- +duced forms. + +**Family 1. Helicoidae.** + +To this family belong only water- or marsh-plants; the endocarp is seeling, and they possess an embryo with a very large hypocotyl prolonged downwards and often club-like. The perianth is often differentiating into calyx and corolla; the flowers are bisexual, and in the first order of the Monocotyledonous type; but in the second order it is reduced to that of the ordinary Monocotyledonous type; there are, however, rarely found two 3-merous whorls of carpels (Fig. 282), and thus in all 6 whorls, or again, more than 6 carpels, but with a very small number of stamens may also be increased, either by the division of the members of a member, or by the development of additional whorls. + +*Sympera*, with nul or follicular fruticita, are very common, for example, in the first order of the last (Hydrocharitaceae) the carpels are very reduced, but they are still 3-merous. + +The primitive type appears to be a hypogynous flower, similar to that of the Juncaginaceae or Alismaceae, with several 3-merous whorls, and free carpels, each with a single stamen. In the first order of the Monocotyledonous type, besides the reduced ones, there is a flower with this structure at the start- +ing point; then the family develops partly into epigynous forms, partly into others which are reduced to one whorl of carpels; these latter can possibly refer to them to the ordinary type. The family, through the peculiar *Zosteraceae*, appears to approach the Araceae, in which Pothosanumaceae and Nolideaceae are included; but it is not clear whether they are related to them or not. The genus *Hypnea* and *Zostera* in the Juncaginaceae appear quite correct. It would scarcely be right to separate *Zostera* from them. Great stress has often been laid upon the supposed relation between *Zostera* and *Alisma*, but it is scarcely more than an analogous resemblance. + +**Order 1. Juncaginaceae.** + +The *Juncus*, regular, hypogynous flowers have the perianth 3+3+3, epigynous, and stamens 3+3+3 (with extreme an- +teriority); in some cases there is a single stamen on each side of the perianth, +one whool may be suppressed (in *Triglochin maritima*) all carpels are developed; in *P. patens* this inner whool is unfertile). Inflores- +cence long spikes. Embryo straight—March plants with radical, +rush-like leaves. Carpels 3-merous (sometimes 2-merous), usually sub- +ligulate ("amnionarum intravaginalis"); the inflorescence is a spike or rucemce—*Schenckia*. Carpels almost free; in each at least + +1 Sympery = cluster of fruits belonging to one flower. + +HELODRIE. 279 + +two ovales. Follicles.—Triloculus has long, fine racemes without bracts or bracteoles; one ovule in each carpel. The carpels in the two native species are united, but separate when ripe as a schizocarp, loosening from below; they open along the ventral sutures and contain a single seed with a large embryo. The most refined is *Lilies* (1-3 sp. Am.)—Prolygonous. About 10 species. + +Tepu. Fossils in Tertiary. + +Only one genus, *Pleurostogonatum*. The aquatic plants belonging to this order are perennial, living entirely submerged, or with floating leaves, and preferring still water. The leaves are alter- +nate, in some linear and grass-like, in others there is an elliptical floating blade, supported by a broad submerged petiole. Axillary scales, or leaf-sheaths, in some a syrphus with seeds or drops; the embryo is curved, of very various forms. +Potamogeton (pond-weed). The rhizome is creeping, sympodial (with two internodes in each shoot-growth); the inflorescence is a terminal panicle of racemes on short peduncles. It was found 2 false-leaves placed nearly at the same height, from whose axils the branching is continued continuously. The flowers are 2, 4- +merous, naked, and consist only of 4 stamens, with the connective, broadly spreading and often reflexed at the base; 2 free pistils, and of a free, sessile carpel. They are common plants in fresh water. The spikes, during the flowering, is raised above the water. Wind-polinated and protogynous; the female flowers are more numerous than the male. The spike has only two naked flowers, each consisting of 3 stamens and 4 carpels. The stalks of the induplicate carpels are considerably prolonged,—denticulate at their extremities. The perianth consists of 4 (3-5) carpels, with membranous, bell-shaped perianth; long-styled; the flower has 1(2) stamens. Atthion (water-lily). *Nelumbo nucifera* is an entire submerged, marine plant with creeping rhizomes (with displacement of buds) and strap-shaped leaves. The flowering shoots are sympodial with displacement of the axes (Fig. 281). The inflorescence is a peculiar, flatly-com- +pressed panicle (Fig. 282), which is produced by the elongation of the peduncles (Fig. 283). This inflorescence may be considered, no doubt correctly, to be derived from the symmetrical spike of Potamogeton by strongly devolitional development, and by a similar reduction of the number of stamens and carpels. Two rows of flowers are developed, but of these one is passed into the other that apparently only one is present. Each flower consists of only 1 stamen and 1 carpel; the latter is sessile and has a long style; its membranous ovary enloses 1 pendulous ovule and bears a bivald style. As regards the perianth (1) one leaf may be present (Z. nana, Fig. 281 D). The pollen-grains are filamentous. Pollination takes + +**Fig. 281. —Kadom. A Diagram of the branching of the third phytoc. f. 1, 2, ... see this successive short-branching, every other one being shaded of the form-nature, sp.** +*At the top of the figure is shown the first branch, which is formed by a single stem with a rounded terminal (the plant axis), proceeding in the axil of a leaf, and giving rise to two branches, one of which is shown at the left, and the other at the right.* +*II, which is borne in the axil of the second leaf, is shown at the left.* +*III, in the axil of the third leaf, is shown at the right.* +*C The upper portion of a young axis with development of flowers. D Part of a specific flower, that part which develops into one member connected by a dotted line.* + +20 + +HELOXIUM. +281 + +place under water. *Fodinum* and *Gymnocheis* are allied to these. About 70 species. + +Order 1. *Aponogetonaceae*. Aquatic plants with tuberous stems. They have a single, terminal petaloid (3-6-leaved, most frequently 5-stamens and 3-6 carpels). Straight embryo.-About 55 species (Africa, Madagascar, Tropical Asia and Australia).—As in the *Liliaceae*, the flowers of these *Heloxiurns* are given on the upper surface of the leaf that has its base, perfoliate leaf-sheath, or a sheath at the base of the stem. Order 2. *Najadaceae*. Only one genus *Najus* (about 10 species); annual from water. The leaves are long, linear, and narrow. The flower is remarkable in having a terminal stem, which has either a longi- +tudinal locule or a central one; on this account the stem of *Najus* is con- +sidered as a modified petiole. The stamens are opposite the petals. The uni- +locular gymnose and the single, erect, anatropous ovules are also bisexual. +Pollination takes place under the water. + +Order 5. *Allismaceae*. The regular, hypogynous flowers are in some species unisexual by the suppression of either androecium or gynoecium. The flowers are usually solitary, but sometimes aggregated into 3 -spals and 3 petals; generally 5 stamens in the outer whorl (by the division of the 3; Fig. 283) and often several 3-merous whorls within them, which may be arranged radially, spirally, or cyclically or spirally. Fruit a syncarp. + +A. Marsh- or water-plants with radical leaves and long-stalked inflorescences. + +B. Flowers with seeds, which are borne on nearly the whole of the inner surface of the cyclic carpell (as in Nympheaceae). Embryo straight or curved (Fig. 282), with a short embryo-sac (Fig. 282), has an umbell (generally composed of 6 helical cymes). S.S., P.3, stamens 9 (4 + 3, i.e. the outer whorl doubled), G.3 + 3. B. umbellettes; creeping rhizome with trilobate leaf-like--*Hydrocotyle*. Limosella. + +B. Alliaceae. Fruit achene. Latex common (in the inter- +cellular spaces). The flowers are arranged mostly in frequent or simple cyme-like clusters; the leaves are strap-shaped.--*Allium* (Fig. 283, d, e) (in 1 whorl), grouped in pairs (i.e., in front of the sepals), and 1 whorl of sessile achenes on a flat receptacle. The leaves are most frequently rudicle, long-stalked; the hairs are short and simple or branched; the anthers are imbricated +veneration. A. plenoculus--*Elaeia* (E. natans) has spirophore (turned inward) ovules, whilst the ovules of *Alisma*, Sagittaria and others +are a protopous (turned outwards).--*Echinodorus* (E. ranunculoides) + +Fig. 280.--Diagram of Heloxium. +Fig. 281.--Diagram of Echinodorus. + +282 + +**MONOCOTYLEDONES** + +has a convex receptacle, carpels many, united and capitate. +*Danzanomus*. - *Sagittaria* (Arrow-head) has numerous flowers, +several whorls of stamens and spirally-arranged scales on a very convex receptacle. The leaves are long and narrow, and are situated at the end of long, submerged branches. The leaves, in deep and rapidly running water, are long and slim-shaped, but in the air arrow-shaped. +*Hymenocallis*. - *Lysichiton* (Yellow Flag) has a few large flowers. *Platycyclus* has 12 nectaries. The submerged flowers of *Eriophorum* sartus remain closed and are self-pollinated. *Brunnera* has protandrous flowers. There are about 30 species of this genus in the Tropics—Trees—Indifferent. + +The rhizomes of some is farinaceous. + +Order 6. **Hydrocharitaceae**. This order differs chiefly from the preceding in its epigynous flowers. These are in general uni- +carnate (carpels united), but in some genera they are 3-carpelled +spathe ; they are 3-margined in all whorls, but the number of whorls is generally greater than 5, sometimes even indefinite. The peri- +anth is divided into calyx and corolla. The corolla is unisexual with +peripheral stamens and central pistil. The fruit is a berry-like capsule. The +fruit is berry-like, but usually retracts irregularly when ripe. Emb- +ryo straight—Most often submerged water-plants, leaves seldom +floating on the surface. Axillary scales (gamoula unirranculans). +*Hydrocharis*. - Floating on the water, with submerged cordate leaves; +*S. P. fah (folded in the bud)*; *S. corymbosa*—3-carpelled; leaves +each spathe ; stamina-6; the most internal sterile. +*S. flava*—4-flowered; three stamens; ovary globose, with many ovules attached to the base of each stamen. +[The name of the +*S. flava* is a noun in apposition.] + +In the following +genus the pollination is without doubt effected by insects.] *B. morsus rana (Frog-tail) has runners; it hibernates by means of special +roots which grow down into the mud, and then up again to the air, +thick, stiff leaves with spiny margin, springing from a short stem, +from which numerous roots descend into the mud. In- +florescence perianth, and every row nearly the same as in *Hydrocharis*, +but the outer 6 are in a whorl (deciduousment), and inside the perianth +in both flowers there are numerous (15–30) nectaries (stamin- +odes). *S. odorata* (Water-soldier); in N. Eur only 2-plants. +*Callitriche*. - Floating on the water, with submerged cordate leaves ; +the flowers are detached from the plant, and rise to the surface of the water, +where they open; the fruit is a capsule with several erect curved peduncles which contract after pollination, so that the *S. flava* is again drawn under the water, and the fruits ripen deeply submerged.—*Elodea canadensis* + +A page from a botanical text book. + +GLYCINACEAE. 2S3 + +It is also an entirely submerged plant. The leaves are arranged in whorls on a well-developed stem. Only 2 species in Europe (introduced about 1859 from N. Am.). This plant spreads with great rapidity throughout the country, the reproduction being effected by means of a root-like rhizome. + +—In many of these genera the number of whorls in the flower is remarkably re- +duced; for example, in *Fenicia*ia, in the $g$-flowers to $2$: Fr. & C. (1 - 3) in the $p$. $b$, $c$, $d$, *Sammannon*, in $a$-flowers to $5$: *Berg*, *Lappo*, and *Lappo*. + +Family 2. GLYCINACEAE. + +The hypogynous flowers in the Juncaceae are completely developed on the protandrous type, with dry, sessile perianth. Even in those the interior whorl of the perianth is suppressed, and the ovary, which in *Juncus* is trilocular with many ovules, becomes in *Luzula* almost unicellular, but still with 3 ovaries. The perianth is reduced to a few scales, or even wanting; the stamens, in the first of these, are nothing; in the flowers at the same time they are more closely on the inflorescence (spike) supported by dry bracts (cauf); the number of stamens is almost constantly 3; stigma linear; the ovary has only 1 locule with 1 ovule; the fruit, which is a cup- +ped nut, is usually becoming woody or carpeloid. In *Juncus* the pericarp is large and horny, the embryo being placed at its lower extremity (Figs. 286 B, 291).—The plants belonging to this order, with the exception of a few species of *Luzula* and *Carex* or perennial herbs. +The stems are erect or round and thin, and for the most part long, +internodes, with linear, parallel-vetined leaves which have long +sheaths, and often a ligule, i.e. a membranous projection, arising transversely from the leaf at the junction of the sheath and blade. +The seeds are small and without any appendages. The flowers are small and insignificant. Wind- or self-pollination. + +Order 1. JUNCACEAE (Rushes). The regular, hermaphrodite, +hypogynous flowers have 3 + 3 brown, +dry, free stamens, which resemble +like a star during the opening of the +flower; stamens 3 + 3 (seldom 3 + 0) +and 3 carpels united into one gynoeceum +(Fig. 285). The perianth is wanting; +there is no rule, a style, which be- +comes divided at the summit into 3 +stigmas, often bearing branches twisted +to the right (Fig. 285).—Fresh capsules +with numerous seeds. The embryo is an extremely small, +ellipsoidal, cellular mass, without differentiation into the external organs. + +**Fig. 285.—Flower of Luzula.** + +284 + +**MONOCOTYLEDONES.** + +*Juncus (Rush) has glabrous foliage-leaves, generally cylindrical, rarely flat; the edges of the leaf-shafts are free ("open" leaf-shafts) and cover one another. The capsule, 1- or 3-locular, with many seeds.* --*Luzula* (Wood-Rush) has flat, grass-like leaves with entire edges; the edges of the leaf-shafts are united ("closed" leaf-shaft). *Carex* (Sedge) is similar to *Luzula*. *Prionium*; *S. Africana*; resembling a *Tecoma*. + +The interior wall of stamens, in some species, disappears partially or entirely; in others, it remains. + +Some of the numerous Juncus-species (e.g. *J. effusus*, *placens*, *concolorum*, etc.), have false lateral inflorescences, the axis of the inflorescence being pushed into one side of the plant, and the flowers being arranged on this side only. This condition of the stem, and resembles it both in external and internal structure. The foliage-leaves of the genus were formerly described as "undulate-stem," because their edges are undulate. In the following species, however, the stem was said to be "leathery"; i.e., *cf. ephusa*, *placens*, *concolorum*. Sterile paraphyllumous cells are found in the pith of these stems and in the leaves. Other genera belonging to this order are: *Eriophorum* (Cotton-grass), *J. balticus* (Tundra rush), *nuphar*, and others. The inflorescences most often present are those which are composed of several branches, each bearing several fertile and sterile axes. Their composition is as follows:---The flowers have either no bractlets, and the inflorescence are then capitulate; or they have 1- several bractlets. Each branch bears 1-2 fertile axes, and 1-2 sterile axes ("intermediate-axes"), and succeeding this are generally several bracteae borne alternately and in the same plane as the branch; the uppermost (the "false-leaves") being always larger than the lower ones. The sterile axes are usually called "bractlets," and are termed "intermediate-axes." If no bractlets occur in the axis of the branch-leaves, then the succeeding branches are always borne on the posterior side of the first branch. In this case, there is only one fertile intermediate-leaf, then the lateral axes are always on the upper side, and a "false" lateral inflorescence occurs; if there are 2 fertile intermediate-axes, then there is a "false" lateral inflorescence; if there are three, being several, then a "moss," or spike. + +*Juncaceae* is a very large family spread among the Liliiflorae, but there are so many morphologically and partly anatomical features agreeing with the two following orders, that they may, no doubt, most properly be regarded as the starting point of a new order. The order is characterized by: 1stly, by the type of flower; the inflorescence, the type of mechanical system, and the stomata. **Pollination** by means of the wind. Cross-pollination is often established by protogyny. 2ndly, by having a single flower on each stem; 3rdly, by having open flowers. --Droseraceae. The 500 species are spread over the entire globe, but especially in cold and temperate countries; they are seldom found in tropical regions. + +Order 2. **Cyperaceae.** The majority are perennial (sedum) + +1 "fan" and "sickle" are adopted as terms for those inflorescences from the German "fachel" and "sickel." + +
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+ +EXOASCI. +117 + +Endomyces decipiens is a parasite in the fruit-body of *Amanita muscaria* and *E. magnum* lives in the gomatines, fermenting exudates of Oak-trees; *Aenocaricium albidum* is found under the bark of the Firs-tree. Endomyces has also been found on *Picea*. The species of *Tapharia* are parasites, whose free ascii may be found in great numbers, generally closely pressed together, on the parts of plants which they have attacked. The ascii are de- +veloped directly from the ascogenous cells of a fertile, generally solitary, ascomycete fungus, called a *perithecium*. The latter arises from the peritingating asciopore, and may hibernate in the tissues of its host, particularly in the winter buds, and then with the commencement of the next period of vegetation it con- +a +b + +Fig. 104. — Typhula (feminine) +prost. *Vimexia*: budding of a +germinating spore (*x 300*). + +times its growth side by side with that of its host. The hyphae +ramify in the intercellular spaces or beneath the cuticle, but have +no haustorium. The asciopores (Fig. 105 A) and urmicel ascii may +produce conidia. + +Very numerous appearances, and swellings of the attacked tissues, are pro- +duced when the mycelium is perennial; for example, the "Witches'-brooms" +and "Pocket"-Forks". The hard, hollow, stone-like plums, known as "Pocket" +Forks", are produced by the growth of the mycelium within the flesh of the fruit; +these are caused particularly by *T. penn.* on several species of *Prunus*. +The "Witches'-brooms" on the contrary, are deformations of entire twigs or +branchlets, which are produced by the growth of a mycelium within the wood, +caused by *T. cephaloïdes* on *Carpinus betulus*, by *T. carpini* on Cherry-trees, +by *T. corni* on Fir-trees, by *T. insititutus* on Birches, by *T. repens* and +*P. rubra*. *T. deformans* attacks the leaves of the Pines, and causes them to curl. + +c +d +e +f + +Fig. 105.—Typhula hispanica: a ascus filled +with conidia; b germinating spores (*x 600*). + +118 +CLEVONIACEAE. +When a perennial mycetium is wanting, the infection is confined as a rule to white or yellow spots on the leaves, e.g., the commoner, *T. nodosum*, on Alnus +plenosa, and *T. aureum* on species of Populus, *T. albidum* (Fig. 108) causes +considerable hypertrophy on the palisade cells of the Alder, which may be +compared in the "pockets" of France. + +Fm. 108.—Thyphera alba (from the Alder (sal. steg.). + +**Series 2. Carpoaceae.** + +The Carpoacei are Ascomycetes, whose ascus are enclosed in fruit- +bodies, i.e. ascocarps. The accessory means of reproduction are +free conidiophores (Fig. 109), conidial-layers (Fig. 122), conidio- +carps (Fig. 120, D, E, etc.), chlamydospores and oidia. + +For the different methods of distributing the ascospores, see p. 92. + +Of the six families of the Carpoacei, the first three—Gymno- +scales, Parigosporales, and Pyrenomycetales—are anagamic (that is, +the ascocarp remains closed throughout its existence and does +not detach itself by rupture); the fourth and fifth (Hypocreales +and Diacoccetae), on the other hand, are hemianagamic (the +ascocarp, here also called an apothecium, is closed in the early +stages, but opens at the commencement of ripening and exposes +a hymenium with free ascus); the sixth family *Clevoideae* has probably +genogamic (or hemianogamic) fruit-bodies. + +**Family 1. Gymnoascales.** + +The ascocarps are surrounded by a spongy and incomplete en- +velope. One order, poor in species, + +Fig. 109.—Thyphera alba (from the Alder (sal. steg.). + +CARPOASIS + +119 + +**Order Gymnosporaceae.—The ascospores are borne sometimes solitarily, or sometimes coiled together. *Gymnospora resinif* small bodies about 1 mm. in diameter on old horse-dung, which at first are white and afterwards orange-red.—Coryneum ascospores live in the old feathers in birds' nests. + +**Family Perisporiales.** + +The ascospores are surrounded by a thick envelope without any opening; the fruit-bodies are cleistocarpous; the spores are only liberated after the disintegration of the fruit-bodies. Paraphyses are wanting. The two first orders have in addition the means of reproduction by means of zoospores. + +*Order Erysiphaceae, Mildews.* The Fungi belonging to this order are epiphytic parasites, whose mycelium, somewhat resembling a cobweb, may be seen on the leaves and other green portions of plants (see Figs. 107, 108). The hypha ramify + + +A small diagram showing a hypha with branches. + + +Fig. 107.—Erysiphe sikkimensis: a mycelium-throate; b antheridium; c zoospore; d zoospore. +In all directions upon the surface of their host, and emit antheridia, which penetrate the epidermal cells, and thus derive the necessary nutrition. The Mildew-Fungi thus belong to the obligate parasites, and during their growth dwarf and destroy the portions of the plant on which they grow. The mildew is often visible to the first instance by abstraction of conidiophores from the end of special branches (Fig. 108 a), a hypha is seen in the act of detaching a conidium). The conidia may germinate immediately, and thus quickly destroy the plant. In some cases, however, where they appear as a white meal covering the surface of the plant on which the fungus is found. Later on appear the dark brown, spheroid ascospores (Fig. 108 a) which, although small, are generally just visible to the naked eye as black specks. + +A characteristic feature of the Mildew-Fungi is the thin, pseudo- + +120 +CLAROASCI. + +parenchymatous covering of the ascocarp, enclosing one (Podo- +sphere) and Sphaeridium compactum, or both, among the Hemi- +cystae) or a few (Fig. 107 c), which do not form a hyphal system, +but are irregularly placed. The cells of the ascocarp-envelope +are often prolonged into hair-like appendages. The ascocarps +are developed from the mycelium at places where two hyphae cross +each other (Fig. 107 b). In some cases, two or more hyphae +are produced side by side. The one from the lower hypha (Fig. +107 c) assumes an ellipsoidal shape, and is cut off by a transverse +wall to form the oogonium; while the other (b) arches over, and + +A diagram showing the structure of a Saprolegnia-like fungus. It shows the apical portion of a leaf with a small portion of the fungus growing upon it. The fungus has a true antheridium at its apex, which produces an oogonium. The nucleus from the antheridium passes into the oogonium, and unites with its contents to form a zygote. The zygote divides by mitosis to produce a binucleate penultimate cell, which then divides again to produce the ascus. The binucleate penultimate cell is known as the ascogone. + +Fig. 108.—Erythrophleum comosum. A small portion of a leaf with this Fungus growing upon it, showing the structure of the fungus. The true antheridium is at the apex of the leaf, but is re- +productive organ of a pyrenomyceteous Fungus parasitic upon it (Cuniculata). + +from its apex the true antheridium is cut off (Fig. 102A). The +nucleus from the antheridium passes into the oogonium, and unites +with its contents to form a zygote. This zygote divides by mitosis to pro- +duce a binucleate penultimate cell, which then divides again to produce the +ascus. In Sphaerothecus the binu- +cleate penultimate cell produces the asca, but in other genera it +branches and gives rise to numerous ascus. Hyphal branches from +the base of the ascogone surround it and form the envelope of the +ascocarp (peel). + +Many plants, both cultivated and wild, are attacked by various + +CARYOGASL. +121 + +species of Mildew. A common means of prevention against their attacks is to dust the diseased parts with sulphur. + +*Sphaeridace* panamensis occurs on the leaves of *Rosa*, and on the fruit of *Pistacia*. *Erysiphe* coryli, on *Corylus* (Cherry-leaves). *Krypsine* tuckeri grows on the leaves and fruit of the *Vine* ; it spines its hyphae over the bunches of grapes, curtails their growth, and causes them to burst, and to become dis- + + +A small round structure with a central cavity, possibly a spore or a young fungus. +B A larger, more complex structure with numerous smaller structures radiating from a central point, possibly a mature fungus or a fruiting body. +C A long, thin structure with a central cavity, possibly a hypha or a root. +D A long, thin structure with a central cavity, possibly a hypha or a root. +E A long, thin structure with a central cavity, possibly a hypha or a root. +F A long, thin structure with a central cavity, possibly a hypha or a root. +G A long, thin structure with a central cavity, possibly a hypha or a root. +H A long, thin structure with a central cavity, possibly a hypha or a root. +I A long, thin structure with a central cavity, possibly a hypha or a root. +J A long, thin structure with a central cavity, possibly a hypha or a root. +K A long, thin structure with a central cavity, possibly a hypha or a root. +L A long, thin structure with a central cavity, possibly a hypha or a root. +M A long, thin structure with a central cavity, possibly a hypha or a root. +N A long, thin structure with a central cavity, possibly a hypha or a root. +O A long, thin structure with a central cavity, possibly a hypha or a root. +P A long, thin structure with a central cavity, possibly a hypha or a root. +Q A long, thin structure with a central cavity, possibly a hypha or a root. +R A long, thin structure with a central cavity, possibly a hypha or a root. +S A long, thin structure with a central cavity, possibly a hypha or a root. +T A long, thin structure with a central cavity, possibly a hypha or a root. +U A long, thin structure with a central cavity, possibly a hypha or a root. +V A long, thin structure with a central cavity, possibly a hypha or a root. +W A long, thin structure with a central cavity, possibly a hypha or a root. +X A long, thin structure with a central cavity, possibly a hypha or a root. +Y A long, thin structure with a central cavity, possibly a hypha or a root. +Z A long, thin structure with a central cavity, possibly a hypha or a root. +AA A long, thin structure with a central cavity, possibly a hypha or a root. +AB A long, thin structure with a central cavity, possibly a hypha or a root. +AC A long, thin structure with a central cavity, possibly a hypha or a root. +AD A long, thin structure with a central cavity, possibly a hypha or a root. +AE A long, thin structure with a central cavity, possibly a hypha or + + +Fig. 109.—*Erysiphe glaucum*: $a$, portion of mycelium lying horizontally; $b$ variably-shaped conidia; $c$, conidium; $d$, conidiophore; $e$, conidiogenous cell; $f$, ripe conidium; $g$, germinating conidium; $h$, germ-tube; $i$, germ-tube in the development of an ascuspore; $j$, stage later; $k$, mature ascuspore; $l$, mature ascuspore at the base of the cell has given off branches which are applied to the sides of the young ascuspore. (Lingamshaw.) The disease was introduced into England in 1845 and later was found in all countries where grapes are grown. It is only known in the comidal form ("Odium tuckeri"). Many other species of Erysiphe are found on herbaceous plants—Microspores have appendages which are regularly formed at their extremities. *Ar* *graminearum* on *Bilis* *graminearum*. + +122 + +122 + +**CARYOSCL** + +*Conidiate has appendages with spirally-celled antennae; on Solis et loc.; — Phylogenetica has a strigus-like appendages with dilated bases. F. guttata on Corylus, Fraxinus, Paeonia, etc.* + +**Order 2. Perisporiaceae.** Moulds and Mildews. A group of Fungi widely distributed and found in all situations. Usually they have a well-developed surface mycelium, and small, round, seldom conical or acrocerous, containing ovules, pulley-like spores. They are partly saprophytes, partly parasites, in the latter condition having a brown mycelium. + +*Euvatorium glaucum (= E. herbaria, Figs. 109, 110) and E. repens live on dead organic matter, produce white or greyish conidial forms of both species, known as "Moulds" (Fig. 108), and formerly were described under the name "Aspergillus glaucus." + +*Fig. 105—Euvatorium glaucum. A longitudinal section of a leaf-stem economy, bounded externally by a thin layer of cells, internally by a thick layer of cells. The outer layer contains the chlorophyll and the inner one the starch granules. In the middle is a large cavity filled with water. The upper part of the figure shows the conidiophore with its conidial head. The lower part shows the conidial head with its conidial heads. The conidia for some time remain attached to each other in chains (Fig. 109 a); they are abstricted from stigmata arranged radially on the spherical, swollen end of the conidiophore. The small yellow or brownish ascospores are frequently found in herbaria, especially when the specimens have been inadequately dried; but they are rare in nature, and others are pathogenic, causing mycoses in warm-blooded animals. + +*Penicillium crustaceum (F. glaucum, Figs. 111, 112) is an ex- +ceedingly common "Mould." Its mycelium appears very fre- +quently on any organic matter which is permitted to remain +unstomached, and soon covers it with a dense mass of blue-green + +A diagram showing the structure of Euvatorium glaucum. +A diagram showing the structure of Penicillium crustaceum. + +123 + +*Clopoacul.* + +*conidiophores.* These branch at their summits and bear flask-shaped cells from which the conidia are abstricted. The ascocarps, which, both in size and colour, resemble grains of sand, have only + + +A small portion of mycelium, produced from a conidium as *, with five conidiophores; a young flask-shaped cell in attaching a conidium; a large conidiophore after 9-30 hours. + + +Fig. 111.—*Pseudolium creatonum*: a conidium (*x 500*); b germination of conidium; c small portion of mycelium, produced from a conidium as *, with five conidiophores; d young flask-shaped cell in attaching a conidium; e the same conidiophore after 9-30 hours. + + +A two spiro-celled hyphae arise from the mycelium (a); b a young flask-shaped cell in the development of the ascocarp; the same flask-shaped cell (b) in attaching a conidium; c a mature flask-shaped cell (c) in the development of the ascocarp; d a mature flask-shaped cell (d) in attaching a conidium; e these are enclosed by a pseu-dopycnium of steric hyphae (*x 500*); f a series of age and with spores; g four ascocarps seen laterally; h germinating ascocarps. + + +Fig. 112.—*Pseudolium creatonum*: a two spiro-celled hyphae arise from the mycelium (a); b a young flask-shaped cell in the development of the ascocarp; the same flask-shaped cell (b) in attaching a conidium; c a mature flask-shaped cell (c) in the development of the ascocarp; d a mature flask-shaped cell (d) in attaching a conidium; e these are enclosed by a pseu-dopycnium of steric hyphae (*x 500*); f a series of age and with spores; g four ascocarps seen laterally; h germinating ascocarps. + +124 + +CARPOASCL. + +been obtained in luxuriant cultivation with a limited supply of oxygen. + +Cigenicium antitum (Fungus antitum, Chalopogonum fumosum), a common mildew, forms dark orange-spots on the leaves and branches of various shrubs (Poplars, Elms, Willows) and on Hops. The conidia appear in various forms, as on cotton-wool, as on the surface of the leaf, and as in the form of a club-like conidium with small unicellular conidia; in nutritive solutions yeast-like conidia are also developed.--Aspergillus pimphilus produces mildew on the leaves of the hop plant ("Huperzia serrata"). (The conidial forms were formerly described as "Aspergillus pimphilus".) + +Order 3. Tubercaceae. Truffles. The Fungi belonging to this order are entirely subterranean. The mycelium is filamentous, and partly parasitic upon the roots of plants, especially trees, in its neighbourhood ; it is then known as *mycorrhiza*. The fruit-body is relatively large, in some cases about the size of a hen's egg. Internally it is traversed by a number of winding passages (Fig. 113 a), the walls of which are coated with the ascii. The saci (d) contain only a small number of spores, and these are set free by the pressure of the surrounding mycelium. + +Tuber melanosporum, T. bremianum, T. atratum, and other species are edible. *Terfezia leonis* and *Chalopogonum microspermum* are also edible. The Truffles are always found in woods and under trees, and disappear when these are dug up. In many countries there is a large number of Truffles which are hunted by specially trained dogs and pigs. + +In *Euphorbia* (Stag-Truffle) the fruit-body has a corky external layer, and is inedible. Some of the species are found in this country. *Zc. punctatum* parasitic on the roots of the Fig. + + +A small illustration showing a cross-section of a tuber, highlighting internal structures. + + +PYRENOMYCETES. +125 + +Family 3. Pyrenomycetes. + +In this family the hymenium is enclosed in small fruit-bodies, peritheci (Fig. 129), which have a roundish or oval eye as small dots. In shape they resemble a globe or a flask with a narrow mouth, through which the spores are ejected (peronocarpic ascocarps). Different kinds of reproduction—conidia, pycnidia (chiefly with microconidia), chlamydospores, and peritheci—are found in the same species, and these facts show that the life-history of these Fungi are so dissimilar, that formally they were considered to be different genera. Ergot furnishes a very good example. + +This family may be subdivided into 3 sub-families. + +A small portion of an ovary attacked with Corsonia purpurea (Ophiostoma). +Fig. 114.—A small portion of an ovary attacked with *Corsonia purpurea* (Ophiostoma). + +An ovary with the conidial stage of *Chlorella purpurea* (Mycodipus). +Fig. 115.—An ovary with the conidial stage of *Chlorella purpurea* (Mycodipus). + +Sub-Family 1. Hypocreales. + +The perithecia are pale, feathery, brightly coloured, and generally aggregated on a stem. Conidia and chlamydospores occur very rarely, or not at all. + +Order. Hypocreaceae. In this order the majority are parasites upon Flowering-plants (*Nectria*, *Polytopium*, *Epiclios*, *Claviceps*); but some are parasites upon Fungi (*Hypomyces*, *Melanose*, *Corynespora*). + +The most important member of this order is the *Eroin* (*Claviceps purpurea*, Figs. 114, 115, 116). This Fungus is found in the flowers of many species of Grasses, especially the Rye, attacking and destroying the ovaries. In the first or corneal stage of the attack, the ovaries are found covered with a white, irregularly + +--- +**Note:** The text appears to be discussing various aspects of fungi within the Pyrenomycetes family, particularly focusing on their reproductive structures and life cycles. It mentions specific types of fungi like *Corsonia purpurea*, *Chlorella purpurea*, and *Eroin* (*Claviceps purpurea*), along with their reproductive stages and habitats. The text also touches on the classification of these fungi into sub-families and orders. + +126 + +PERLONOMICEYES. + +folded mycelium (Fig. 114 a, Fig. 115), formed of numerous hyphae woven together and projecting into the wall of the ovary. +From these a number of hyphae (Fig. 114 e) project into the air and abstract from their apices the conidia (b) which serve as repro- +ductive organs. The mycelium also secretes a sticky, stinking fluid (Fig. 115 b), which attracts flies, and by means of this +number. The honey-dew exudes from the bases of the glumes, +and is greedily sought by flies, which thus carry the conidia to +other ovaries. In this manner fresh ears are infected, which might + + +A: A sclerotium surrounded by the eight filamentous conidiophores emerging. +B: A sclerotium surrounded by the eight filamentous conidiophores emerging. +C: A sclerotium surrounded by the eight filamentous conidiophores emerging. +D: A sclerotium surrounded by the eight filamentous conidiophores emerging. +E: A sclerotium surrounded by the eight filamentous conidiophores emerging. +F: A sclerotium surrounded by the eight filamentous conidiophores emerging. +G: A sclerotium surrounded by the eight filamentous conidiophores emerging. +H: A sclerotium surrounded by the eight filamentous conidiophores emerging. +I: A sclerotium surrounded by the eight filamentous conidiophores emerging. +J: A sclerotium surrounded by the eight filamentous conidiophores emerging. +K: A sclerotium surrounded by the eight filamentous conidiophores emerging. +L: A sclerotium surrounded by the eight filamentous conidiophores emerging. +M: A sclerotium surrounded by the eight filamentous conidiophores emerging. +N: A sclerotium surrounded by the eight filamentous conidiophores emerging. +O: A sclerotium surrounded by the eight filamentous conidiophores emerging. +P: A sclerotium surrounded by the eight filamentous conidiophores emerging. +Q: A sclerotium surrounded by the eight filamentous conidiophores emerging. +R: A sclerotium surrounded by the eight filamentous conidiophores emerging. +S: A sclerotium surrounded by the eight filamentous conidiophores emerging. +T: A sclerotium surrounded by the eight filamentous conidiophores emerging. +U: A sclerotium surrounded by the eight filamentous conidiophores emerging. +V: A sclerotium surrounded by the eight filamentous conidiophores emerging. +W: A sclerotium surrounded by the eight filamentous conidiophores emerging. +X: A sclerotium surrounded by the eight filamentous conidiophores emerging. +Y: A sclerotium surrounded by the eight filamentous conidiophores emerging. +Z: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AA: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AB: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AC: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AD: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AE: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AF: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AG: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AH: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AI: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AJ: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AK: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AL: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AM: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AN: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AO: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AP: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AQ: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AR: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AS: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AT: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AU: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AV: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AW: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AX: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AY: A sclerotium surrounded by the eight filamentous conidiophores emerging. +AZ: A sclerotium surrounded by the eight filamentous conidiophores emerging. +BA: A sclerotium surrounded by the eight filamentous conidiophores emerging. +BB: A sclerotium surrounded by the eight filamentous conidiophores emerging. +BC: A sclerotium surrounded by the eight filamentous conidiophores emerging. +BD: A sclerotium surrounded by the eight filamentous conidiophores emerging. +BE: A sclerotium surrounded by the eight filamentous conidiophores emerging. +BF: A sclerotium surrounded by the eight filamentous conidiophores emerging. +BG: A sclerotium surrounded by the eight filamentous conidiophores emerging. +BH: A sclerotium surrounded by the eight filamentous conidiophores emerging. +BI: A sclerotium surrounded by the eight filamentous con idiophares eme +BJ: A scelotum surro +BK: An +BL: +BM: +BN: +BO: +BP: +BQ: +BR: +BS: +BT: +BU: +BV: +BW: +BX: +BY: +BZ: + +Fig. 114.-Ceratonia purpurea. *A* Scleromycete with ascocarps (d) (c up). *B* Scleromycete longitudinal section of ascocarps (c). *C* *A* showing a single ascus with four spore-like hyphae (k). *D* *A* sacro cupulated, with its eutin filaments encircling emergent. + +escape were the conidia only distributed by wind. This stage formerly was regarded as an independent Fungus, known as Spila- +cides or Spilacidaceae, but it is now considered to be merely a stage either a new mycelium (Fig. 114 d, e), or new conidia. The second or SCLEOTUM stage is in one in which this Fungus passes into winter. The myceliun penetrates deeper and deeper into attacked ovaries, their tissues are destroyed and replaced by hyphal, which gradually become more and more folded together. + +1 + +**PERENNIBICETES.** + +A fern, pseudo-parenchymatous mass of hyphae is thus formed at the base of the loosely-woven *Sphacelus*, which in part trans-formed into the hard sclerotium, and the remainder thrown off. +A dark, hard, poisonous body, longer than the natural grain, is thus formed; these bodies are known as Ergots, and were formerly called *Scilla cornutum.* Ergot, Fig. 116 A, c). The third stage, described as *Claviceps purpurea,* is developed in the following spring from the germinating sclerotium, which produces dark-redstromata with a yellowish-brown margin. In this stage, both ascus and ascospores are produced. The latter may infect young leaves of the cereals, in which the disease is then developed as before. + +A diagram showing a cross-section of a plant with a dark red stroma. + +Fig. 117.—*Neurospora cinerea*; a branch of *Asarum perfoliatum*, with conidial-layers on its peristome (see, also), &c. a conidial-layer (Tetradesmum subspicatum) &c. a mass of peridial spores. + +Several species of the genus *Neurospora*, with blood-red particulates, are found as dangerous parasite, especially *N. ditissima*, which causes "Canker" in the Beech, Ash, and Apple, etc.; *N. cerealis*, which aggresses on Pine-trees, and *N. purpurea*, which attacks the *Rosa*. The latter is often called *Purpurea rubra.* *Fusarium rubrum* forms shining red spots on the green leaves of *Fraxinus-occidentalis.* *Eichhornia tuberiformis* is parasitic on the sheath of Gramaceae, on which it forms a blackish-brown spot. *Phytophthora infestans* is parasitic on potato plants; *Ophiostoma ulmi* attacks the elm; *Gryposis Fungus*, Figs. 118, 119) lives in and destroys insects, and after encompassing their death produces the club-shaped, generally yellow, stromata, on which numerous spores are formed. The *Cystoseira* on the bark of trees (Fig. 119) on the chrysildae and caterpillars of moths, is the most common. + +K + +128 +PERENOMYCETES. + +The so-called *Botrytis brassicae*, which produces the disease known by the name of "Mussardine," in silkworms, is probably a conidial form belonging to *Cordyceps*. + +I. Fig. 126.--*Cordyceps militaris*. I A conidium with conidiophores (1), II A conidium with ascospores, bearing paraphyses. III A spore. + +II. Fig. 127.--*Cordyceps vitellina* on the larva of *Buprestis streusma*: a stalk of atcoma; b--paraphyses. + +A detailed illustration showing the life cycle of *Cordyceps militaris*. The illustration includes three main parts: I shows a conidium with conidiophores, II shows a conidium with ascospores and paraphyses, and III shows a spore. + +PERENOMYCETES. +120 + +Sub.Family 2. *Sphaeriales*. + +To this sub-family belong the majority of the Pyrenomycetes. The paraphyses are of a firm consistency (tough, leathery, woody or carbonaceous), and of a dark colour. Their covering is quite dis- +tinct from the stroma when this structure is present. The strontata are sometimes very large, and may be either cushion-like, crus- +taceous, or of a leafy, branching, bush-like form; or small, +small, inconspicuous Fungi, living on dead vegetable matter, +sometimes parasites. Free conidiophores and conidiospores +are known in many species, and in several, chlamydospore-like forms of reproduction. Orders 3-18 constitute the Sphaerioceae of older systematists. + + +A small, round, brownish object with a central hole, surrounded by a thin, white ring. + + +Fig. 175.—Chlamydospore—e. a portion of an ab-branch with the base partly thrown off; on the wand are numerous black perithecia (a to c). b longitudinal section through a branch of a conidiophore showing the conidia (d) and the spore-sac (e). c. A conidiospore whose ascospores are being ejected—a portion of the same, with hyphae and spores. +Order 1. *Sordariaeae*. — Fungi living on dung with fragile perithecia, either aerial or buried in the substratum. The dark brown or black spores have +characteristic ornamentation (Fig. 176), which is often very conspicuous (Fede- +guesi), by means of which their expulsion and distribution are promoted. + +Order 2. *Chetomycaceae*. — Perithecia fragile, free, bearing on the summit a +terminal or lateral appendage. + +Orders 3–7. — Perithecia scattered or aggregated, situated from the commence- +ment on the surface of the substratum. + +Order 8. *Tetrarhizaceae*. — *Zygosphaeria parasitica* (Fig. 121), on +Alnus alba ; Herpotrichia nigra on Picea excelsa and Pinus montana. + +Order 9. *Trichosporaceae*. + +130 +PYRENOMYCETES. + +Order 4. *Melanommaceae*. *Melanomma quercina* lives in the roots of 1-8-year-old Oaks, and destroys the plants. +Order 5. *Ceratostomaceae*. +Order 6. *Amphiphragmaceae*. *Sirethella obduens* (Fig. 120) has brichid spores, which are attached on the hard branches of Fraxinus. +Order 7. *Lophiostomaceae*. +Order 8. *Cucurbitaricaceae*. *Furcillaria tubulif*, at first embedded, then breaking out of the soil, and growing up to a height of 1-2 feet. +Orders 9-13. The perithecia remain embedded, and are only liberated by the cutting of the plant, or by the action of water. +Order 9. *Spharidaceae*. The species of Spharidella have coloburnia, biocellular spores. They live upon the leaves of many plants, and develop globular perithecia. +Order 10. *Pleosporaceae*. The conidiial-forms of *Pleospora herbarum* and *F. vulgaris* form a black covering on various plants, known as "smuts".--- + +a b c d + +Fig. 121.—Trichoderma porosum: a a twig of diffee alba with epiphytic syringium; b a leaf of *Acer campestre* and sporangia imbedded; c a perithecium (a cut); d a section with spores (x 200). +*Furcillaria atricula* occurs on the underside of dry Boleh leaves, and perhaps to this belong the species *F. fusca*, *Fuscellidium purpureum*, which causes the "Bust-spots" on Apple and Pears. +Order 11. *Masaariaceae*. +Order 12. *Gymnosporangium*. +Order 13. *Gremoniaceae*. Perithecia, with peak-like aperture. *Gremonia erghorotoma* in the leaves of *Prunus armeni*, which turn brown and do no fall in autumn. +Orders 14-18. Strama generally well developed. The perithecia are embedded in the strama, when they are rudimentary, in the substratum. +Order 14. *Valonia*. +Order 15. *Diatrypaceae*. *Diatrysps*. +Order 16. *Melanomniaceae*. +Order 17. *Medegrammataceae*. + +Strama generally well developed. The perithecia are embedded in the strama, when they are rudimentary, in the substratum. + +Order 14. Valonia. +Order 15. Diatrypaceae. Diatrysps. +Order 16. Melanomniaceae. +Order 17. Medegrammataceae. + +PERENNOMYCETES. +131 + +Order 18. *Xylariaceae*. This order is the most highly de- +veloped of the Sphaeriales. The stroma arises on the surface of +the substratum, which is generally dead or decorticated wood; it is well-developed, conical, hemispherical or upright. In +the latter case it is covered with a layer of mycelium, and +later on it bears the *perithecia*, arranged in a layer immediately +beneath its surface. The ascospores are of a dark colour. Often +also there are free conidiophores. + + +A: A conidium. +B: A conidium. +C: A conidium. +D: A conidium. +E: A conidium. +F: A conidium. +G: A conidium. +H: A conidium. +I: A conidium. +J: A conidium. +K: A conidium. +L: A conidium. +M: A conidium. +N: A conidium. +O: A conidium. +P: A conidium. +Q: A conidium. +R: A conidium. +S: A conidium. +T: A conidium. +U: A conidium. +V: A conidium. +W: A conidium. +X: A conidium. +Y: A conidium. +Z: A conidium. +AA: A conidium. +AB: A conidium. +AC: A conidium. +AD: A conidium. +AE: A conidium. +AF: A conidium. +AG: A conidium. +AH: A conidium. +AI: A conidium. +AJ: A conidium. +AK: A conidium. +AL: A conidium. +AM: A conidium. +AN: A conidium. +AO: A conidium. +AP: A conidium. +AQ: A conidium. +AR: A conidium. +AS: A conidium. +AT: A conidium. +AU: A conidium. +AV: A conidium. +AW: A conidium. +AX: A conidium. +AY: A conidium. +AZ: A conidium. +BA: A conidium. +BB: A conidium. +BC: A conidium. +BD: A conidium. +BE: A conidium. +BF: A conidium. +BG: A conidium. +BH: A conidium. +BI: A conidium. +BJ: A conidium. +BK: A conidium. +BL: A conidium. +BM: A conidium. +BN: A conidium. +BO: A conidium. +BP: A conidium. +BQ: A conidium. +BR: A conidium. +BS: A conidium. +BT: A conidium. +BU: A conidium. +BV: A conidium. +BW: A conidium. +BX: A conidium. +BY: A conidium. +BZ: A conidium. + +Fig. 122.—*Xylaria* hyphomycete (red line) on a tree stump : a *peronosporum*, b an other stroma, both of which, with the exception of the black lower portion, are covered with white +conidia. The black portion is composed of *perithecia*, which have fallen off, +a large branched stroma ; c a *conidia*. + +*Hyphomycetum* and *Tunicella* have a cord-like or cruciform stroma.—*Xylaria* +has a more or less cylindrical stroma, or several centimeters high. *X.* +*hygrospora* (Fig. 123) and *X.* *polyporinae* occur on old tree stumps.—*Peronospora* +grows on old horse dung, and has a connal stroma. + +Sub-Family 3. *Dothideales*. + +The *perithecia* are always embedded in a black stroma, and are +not distinctly separated from it. The accessory forms of reproduc- +tion are : comitophores, comitocarps, and yeast-like *conidia*. The +mycelia are often very abundant. + +Order Dothideaceae. *Phylographa genninii* produces acal-like patches on the leaves of the Grasses.—*Sicciria rimos* grows on the leaf-shoots of +*Phragmites*.—*Phylographa petrida* on *Feridian agilinus*. + + +A small image showing a plant leaf with a patch of acal-like growths on it. + +132 + +**DICOCECETES.** + +**Family 4. Hysteriales.** + +This family, like the following, has hemibiontic ascomycetous (apothecia). These are closed in their early stages, but when ripe open in a calyculus manner by a longitudinal fissure; they are black, oblong, and often twisted. Some species are parasites, especially upon the Coniferae. + +Order 1. Hysteriaceae. *Hysterium pulicarum* upon the ruptured bark of many trees. + +Order 2. Hypodermaceae. The species of *Lophoderminum* live upon the leaves of Coniferae, and are the cause of their falling off (Shirley). *L. pinastri* + +a b c + +Fig. 133.—*Lophoderminum* (Hysterotheca) pulicaria. A two-leaves of *Pinus* abies; a two-leaves of *Abies alba* seen from above with xylem; b a leaf of *Picea excelsa* seen from below with xylem; c the underside with apotecia on the upper side with pyriform sporophores. (*x 200*) + +Fig. 134.—Three leaves of *Pinus strobus*. The lower one is covered with *Lophoderminum* warreneri; a under side of the leaves with apothecia; b upper side with apothecia; c upper side with pyriform sporophores. (*x 200*) + +Fig. 135.—The leaves of *Pinus* and *Picea*: the leaves become red-brown, and fall off; first conidiomycetes are formed, and later apothecia; *L. serotinum* (Fig. 128), on *Abies alba*; *L. macrosporum* (Fig. 124), on *Picea excelsa*; + +Order 4. Diococcaceae. + +Order 5. Acropermaceae. + +The ascocarps (apothecia) are at first closed, and only open at the time of their ripening, not valvularly, but more or less + +**Family 5. Discomycetes.** + +The ascomycetous (apothecia) are at first closed, and only open at the time of their ripening, not valvularly, but more or less + +DISCOMYCETES. +133 + +like a saucer or cup, so that the hymenium lies exposed on their upper surface. In the first three sub-families, and generally also in the fourth, the apothecia are formed inside the substratum. The apothecia are, in contrast to the Pyrenomycetes, light and brightly coloured, and contain sizes very small, and may be even invisible to the naked eye. Particles of dust are present between the ascii; they often contain colouring matter, and give to the disc its characteristic colour. The tissue on which the ascii are borne is known as the eypothecium. The shape and colour of the hymenium vary greatly in the Pyrenomycetes. The conso- +forms of reproduction are conidia (sometimes of two forms), chlamydospores, and oidia. The family is divided into 5 sub- +families. + +Sub-Family 1. Phacidiales. + +The apothecia are developed in the interior of the substratum, which they break through, and in general deliquesce apically. The envelope is tough and black. Hypothecium inconspicuous; hymenium flat. + +Order 1. Euphacidiales. *Phacidium alchemutum*, on the leaves of *Ailus alchemutum*. Conidiophores and conidia are found on the margins on the green leaves, while the apothecia are developed on the fallen leaves and deliquesce in the following spring. *E. oeserianum* causes black spots on the leaves of the Syn- +cerae, and is a common parasite. + +Order 2. Pseudophacidiales. + +Sub-Family 2. Stictidales. + +The apothecia when ripe break through the substratum which forms a border round it. Hymenium generally saucer-shaped. + +Order 1. Stictidaceae. *Stictis*. + +Order 2. Oatropaceae. *Oatropus*. + +Sub-Family 3. Tryblidiales. + +The apothecia are embedded in the substratum in the early stages, and then are raised high above it. Hypothecium thick. +Hymenium thin. + +Order 1. Tryblidaceae. *Trybliodon*. + +Order 2. *Heterosporaceae*. *Heterospora patella* on the dead stalks of Umbellifers. + +A diagram showing a cross-section of a discomycete fruit body with an apothecium embedded in the substrate. + +134 + +DISCOMYCETES. + +Sub-Family 4. *Dermateales*. +The apothecium in the early stages are embedded in the sub- +stratum and then break through it, or are from the first situated +on the surface of the substratum. Hypothecium thick. + +Order 1. *Dermatellaceae*. *Dermatella*. +Order 2. *Dermateaceae*. *Dermatella*, *Peltotella*, *Bistrotella*, *Patellaria*. +Order 3. *Arthoniaceae*. *Arthonia* on the bark of trees. +Order 5. *Arthoniaceae*. *Arthonia* on the bark of several trees. *Cotidium* +stictorum on the apothecium of *Scuticium pulmonaria*. +Order 6. *Corticiaceae*. *Corticius* numerous under moist conditions, and +horny when dried.—*Cultura funereaideris*: the red apothecia break out in the +spring on the dried stalks of *Urtica dioica*: a glabrous reproductive form of +the fungus, which is very similar to that of *Corticius* (formerly +described as "Darymoporus virion").—*Barbatia impulsa* on the living or +fallen trunks of Oaks and Beeches. + +Sub-Family 5. *Pezizales*. +The apothecium are developed on the surface of the substratum and +are waxy or flaccid; at the commencement closed, and covered with +a nanceor or cap-shaped, seldom flat, hymenium. The Hypothecium +is generally well developed. This sub-family is the richest in + + +A small illustration showing a small, cup-like structure with a stem-like appendage extending upwards from its base. The structure appears to be a microscopic view of a fungal spore or fruiting body. + + +Fig. 187.—*Peziza cernua*: a slightly +margined, or even highly margined, or +marginating conidiomata. + +Fig. 188.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 189.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 190.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 191.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 192.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 193.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 194.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 195.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 196.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 197.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 198.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 199.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 200.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 201.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 202.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 203.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 204.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 205.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 206.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 207.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 208.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 209.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 210.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 211.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 212.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 213.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 214.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 215.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 216.—*Sclerotinia fusca*: a sole- +margined, or even highly margined, or +marginating conidiomata. + +Fig. 217.—*Sclerotinia fusca*: a sole- +marginated, or even highly margined, or +marginating conidiomata. + +Fig. 218.—*Sclerotinia fusca*: a sole- +marginated, or even highly margined, or +marginating conidiomata. + +Fig. 219.—*Sclerotinia fusca*: a sole- +marginated, or even highly margined, or +marginating conidiomata. + +Fig. 220.—*Sclerotinia fusca*: a sole- +marginated, or even highly margined, or +marginating conidiomata. + +Fig. 221.—*Sclerotinia fusca*: a sole- +marginated, or even highly margined, or +marginating conidiomata. + +Fig. 222.—*Sclerotinia fusca*: a sole- +marginated, or even highly margined, or +marginating conidiomata. + +Fig. 223.—*Sclerotinia fusca*: a sole- +marginated, or even highly margined, or +marginating conidiomata. + +Fig. 224.—*Sclerotinia fusca*: a sole- +marginated, or even highly margined, or +marginating conidiomata. + +Fig. 225.—*Sclerotinia fusca*: a sole- +marginated, or even highly margined, or +marginating conidiomata. + +Fig. 226.—*Sclerotinia fusca*: a sole- +marginated, or even highly margined, or +marginating conidiomata. + +Fig. 227.—*Sclerotinia fusca*: a sole- +marginated, or even highly margined, +or marginating conidiomata. + +Fig. 228.—*Sclerotinia fusca*: a sole-marginated, +or even highly marginated, +or marginating conidiomata + +4 + +DISCOMYCETES. 135 + +species of the Discomycetes and contains forms of very different habit. They grow upon dead wood, upon the ground, and upon dung. A few are parasitic. + +Order 1. **Helotiaceae.** Apothecia with waxy envelope of colourless, or yellowish prothallus-cells. *Chlorocoleium* occurs on the bark of decaying wood (particularly Oak and Banyan), to which it is given a green tinge; the apothecia are developed upon the host-plant and from which, after a period of rest, the long curved spores are discharged. *Helotium* (Fig. 171) is parasitic on Clover; *S. sclerotiorum*, on Datura-roots, *Phalaris*, etc.; *S. fec- erum*, on the berries of *Festucairea mystacifolia*. *Ditrogyne diversa* is a common parasite upon the roots of *Cynodon dactylon*. In *f. falciforme* (Fig. 171) *Helotium* ferrum lives on dry plant stems.—Discomyces williamsoni.—Discomyces williamsoni. + +Larch-anker on the bark of the Larch. + + +A: Helotium obsoletum: a sclerotium with three apothecia slightly magnified; b, same with eight apothecia; c, germinating mycelium. +B: Discomyces williamsoni: a portion of bark of Larch decaying with two apothecia. +C: Sclerotiorum: a sclerotium (oval shape); b, two paraphyses on either side of a conidium with eight apothecia. + + +Order 2. **Mollisiaceae.** Mollisia erecta, principally on decaying wood. + +Order 3. **Perizizaceae.** This order contains the largest and morphologically the highest forms of the Discomycetes. Apothecia fleshly, and in the later conditions generally saucer-shaped. + +*Peziza*, with sessile apothecia, growing on the ground; *P. cochlearis* is brown, and often has a white margin; *P. scabrida* is scarlet; *P. aurantiaca* occurs as an orange-coloured expansion on the ground. + +Order 4. **Ascobolaceae.** Apothecia fleshly; in the later stages flat or + +136 + +**Helvelles.** + +convex. The asci are, comparatively speaking, large, and often contain a great number of spores which escape by the casting off of a lid at the summit of the ascus. Generally living on dung—*Asterolea forficulina*, etc. + +Family 6. **Helvelles.** + +These Fungi have the appearance of clubs, bells, or mushrooms, consisting of an upright stalk or stipe, with a large, flat, and round, on the exterior surface of which the hymenium sporulates. The stipe-caps are probably gymnosporous from the beginning, and on this account these plants are placed in a separate group (Order 10). The *Marcella* (Marcelli) grown on the ground; some species are edible. 1 order. + +Order 10. **Helvelles.** *Spathulae* in yellow and brownish colors, growing on the ground in woods.—*Geoglossum* (Earth-tongue) projects above the ground as a black tongue, or as a small bulbous body; grows in woods and meadows and on heaths.—*Helvella* has a stalk, bearing an irregularly folded head, on which grow the spores; grows in woods and meadows.—*Marcella* (Marcelli) (10), the still stalked head, the external surface of which is reticu- +late and bears the asci—*Mitrula*. Perfo. + +**Appendix to the Ascomycetes :** + +**Family 7. Aiolichenes (Lichen-forming Ascymycetes).** + +The Lichens were formerly classed among the Thallophyta as a group quite distinct from the Alga and Fungi. Investigations dur- +ing the last century have shown that they are not so distinct; that the Lichens are Fungi which reproduce in the same manner as the Ascomycetes, or, more rarely, the Basidiomycetes, and have entered into a peculiar symbiotic relation with Alga, especially the Cyanophyceae; and that without them they would perish and without which they would be unable to exist. The Fungus forms the largest portion of the Lichen, excluding the Alga with which it may be said to be commensal. The Fungus especially produces reproductive organs which produce the inconspicuous growth through the rhizoids, whilst the Alga supplies it with the organic materials. In consequence of this the Lichens, in con- + +ACCOLICHENES. 137 + +tendistinction to other Fungi, need light for the development of their nutritive organs, and are therefore, in any case internally, of a more or less greenish colour. The form and condition of the thallus is unusual among the Fungi, and they can grow upon rocks- or earth-surface without any food organic matter, such as would be required by other Fungi, if soil is lacking. + +Two cellular forms are therefore to be found in each Lichen I. The cells which belong to the Fungus. These are generally septate, branched hyphae without any trace of chlorophyll. In + + +A diagram showing the structure of a thallus. It includes a rhizoid layer (r-r), a medullary layer (m-m), an external layer (e-e), and a cortex (c-c). The diagram also shows the arrangement of hyphae within these layers. + + +Fig. 131.--Transverse section through the thallus of *Stereis fuliginosa* (*x 500*). r-r rhizoid-layer, which arise from the under side; p-p geminal layer; m-medullary layer; e-e upper, external layer; c-c cortex. + +the thallus of the majority of Lichens there may be found a medullary layer (Fig. 131 m) of loosely-woven hyphae between which there are large air chambers; and an external layer (cortex) (Fig. 131 e, e) formed of closely-woven hyphae without any stratification. In some Lichens, however, the outermost hyphae wind about in the thallus, being equally distributed throughout, without forming any decided strata. These Lichens moreover be- + +138 + +ASCOCLENCHES. + +some gelatinous when exposed to moisture (Fig. 132), on account of the swelling of the walls of the algae. The hyphae contain protoplasm with drops of oil, but never starch; their walls easily swell when exposed to damp after having been dried, and in some (e.g. *Cetraria islandica*) they become gelatinous when cooked. Certain algae, however, such as *Chlorella* and *Scytonema*, are not alone, from which it is inferred that the wall is allied, in its chemical nature, to starch. + +2. The enclosed Algae, termed "gonidia." Some belonging to the Cyanophyceae, Protococcaceae, (especially *Pleurococcus*) and + +Cyanobacteria under microscope. +Fig. 132.—*Cetraria* maritima. Transverse section through the thallus, a extreme of tridactyle with excurrent stolonoid; & botio chlamy; & hyphal. + +Chroococcaceae, are spherical and are found isolated, or in irregular groups of two or three (Fig. 132 p.); some belonging to Nostoc (Fig. 132 p.), Lympnaea (Fig. 132 p.), and *Nostoc* in the soil. Each thallus, as a rule, has only one definite Algal-form for its gonidia. + +The gonidia either lie together in a certain stratum between the cortex and the medullary layer (Fig. 132 p.), or are scattered irregularly throughout the whole thallus (Fig. 132). The thallus is in the first instance termed "heteromorous," in the second instance, "homiomorous." The Fungal-hyphae embrace the gonidia and apply themselves closely to, or even penetrate them, and hence it has been difficult to decide whether the one cellular form does or does not develop from the other (Figs. 134, 135). + +6 + +130 + +**ASCOLICHENES.** + +This theory regarding the symbiosis of Fungi and Algae to form a Lichen is termed the Schwendenerian theory, after the first scientist who advanced it with any weight. It had been strenuously inadvised by De Bary, and further arguments in its favor have not been added by Berzel, Stahl, Trend, Frank, Romler, Alfa Müller and others. + +A diagram showing the structure of a lichen. +Fig. 13a.—Vector lichens, which is attached by a permineral thread (5) of Calamus glaucus. + +A diagram showing the germination process of Physcia pericarina with Protoplasma viride. A Syzygium syzygophyllum with Gloeocystis. C Chloridium Jervell with Proto-plasma viride. +Fig. 13b.—A germinating spore of Physcia pericarina with Protoplasma viride. A Syzygium syzygophyllum with Gloeocystis. C Chloridium Jervell with Proto-plasma viride. + +The thallus of the Lichens appears mainly under three forms— + +The *Cirrocarnes*, which adhere firmly to the substratum ( bark, stone) throughout its entire surface, without being raised into any free patches or lobes. It has, in many instances, no definite outline, and hyphal-branches from it often penetrate + +A diagram showing the structure of a lichen thallus. +The thallus of the Lichens appears mainly under three forms— +The *Cirrocarnes*, which adhere firmly to the substratum (bark, stone) throughout its entire surface, without being raised into any free patches or lobes. It has, in many instances, no definite outline, and hyphal-branches from it often penetrate + +140 + +AROCHLINES. + +deeply into the substratum. It grows at the circumference and sometimes dies away in the centre (Figs. 138, 139, 140). + +2. The *Folaceus*. This also lies flat upon the substratum, but is not firmly attached to it and has a definite outline. It grows + + +A diagram showing the structure of a folaceous lichen. + + +Fig. 137.—Folacium of a *Glechoma*, *Lemnaea* and *Porellina*. Drawings & Schematics: +a, b, various species of *Porosella* ; c, *Fernando* in its younger and older condition ; d, *Lemnaea*. +at the margin, and raises itself a little by free outgrowths and lobes (Fig. 141). The rhizoid-strands spring out from its whitish under surface (Fig. 131, r). + +3. The *Particius*, which is attached to its substratum at a small point from which it projects freely, either erect or pendulous. It is more or less tufted, in the form of a bush (Figs. 142, + + +A diagram showing the structure of a particius lichen. + + +Fig. 138.—Lemnaea subfusca, +a the bark on which it is situate ; +b, the leaf with the +necrophy ; f an ascospore. +143). These three thallus-forms gradually pass over by many intermediate forms into one another. + +The Lichens, like other Ascomycetes, have very variously + +**ASCOLICHENES.** 141 + +constructed ascospores (Fig. 197), which are enclosed in ascid (Fig. 196), usually surrounded by paraphyses attached together. They also possess spermatia (Fig. 141) containing numerous spermata. These are by some considered as pyrenidia and microconidia, Möller having shown that the microconidia under certain conditions may be produced from the spermatia, and then with new conidia, just as in other Ascomycetes. This, however, does not disprove the sexual nature of these spores. + +(The development of the ascocarps (apothecia) from carpogonia, as in the Floridae, which was first shown by Stahl, has lately been more fully established. *Colletium* may be taken as a type of + + +A small illustration showing a structure labeled A, B, C, D. + + +**Fig. 184a.—Colletium stipitatum.**      Carpo-                                                                                                                         &bsp; +(1) x 800 ; (2) apex of the trichogyne ; +(3) base of the trichogyne ; +(4) apex of the thallus ; +(5) base of the thallus . +(After E. Baur.) + + +the origin of those attached to the *C. stipitatum*. The carpogonium is a multicellular filament terminating in a trichogyne which projects slightly above the surface of the thallus, while the lower part is spirally coiled and embedded in the tissue (Figs. 182, + +The origin of those attached to the *C. stipitatum*. The carpogonium is a multicellular filament terminating in a trichogyne which projects slightly above the surface of the thallus, while the lower part is spirally coiled and embedded in the tissue (Figs. 182, + +142 +**ACOLOICHENES.** + +(140A). The cells of the carpogonium contain one nucleus, and communicate with one another by means of pits in the wall. + +The spermatium descends into the trichogyne, becomes affected to the tip of the trichogyne and empty its contents into it. After this conjunction has taken place the trichogyne withers, the coiled cells now divide and constitute an ascocene, from which the ascogenous cells are produced. The paraphyses proceed from two or three cells at the base of the trichogyne. + +**Vegetative Reproduction** takes place by *soredia*, which to the naked eye appear as whitish powder on the surface of the thallus. They are formed by the union of two or more groups of gonidia, which are surrounded by a mass of fleshy hyphae. When rupture of the cortex they are set free, and readily carried by the wind to other places, where under favourable circumstances they establish a new thallus. + +A small thallus with soredia and ophelosporous. (Magnified.) + +Fig. 140.—A portion of the thallus of *Parasola pectinata* with *soredia* (a) and *ophelospora* (b), and a portion of a *soredium* (c) showing the *soredia* (d) and *ophelospora* (e) at end of small thallus. C is hole with spongonia and ophelosporous. (Magnified.) + +**Geographical Distribution.** The Lichenæ are the most hardy plants, and are the first to appear on hitherto bare rocks which they grow upon, disintegrate and form a crust over which the growth of other plants may take place. They are to be found from the Polar regions to the Equator; from the highest snow-free mountain-peaks down to the level of the sea; on the stems of trees; on rocks, soil, some even on living plants; also in mosses in running streams, and on stones but they never form thick patches upon green reed-moss. Some grow progressively in enormous masses, and form wide-stretching carpets, e.g., *Reindeer Moss* (*Cladonia rangiferina*), species of *Cetraria* and other fruticose Lichenæ. + +**Uses.** On account of the cell-wall being composed of Lichen- + +142A + +starch (Echinium), the Iceland-Lichen and Manna-Lichen (Lecanora arculata) are used as food; the latter grows on stones, in the deserts of Asia and North Africa, and is often torn loose in large masses and carried away by the wind. The Reindeer-Lichen is not only the principal food of the reindeer, but it is also used in the preparation of the leather of the reindeer. The Lichens of the islands are OFFICIAL. Colouring materials (haemac, urreille, persio) are made from several species, especially from Roccella victoriae (from the rocky coasts of the Mediterranean). Parmelia and Parmelia are used for tanning. Other lichens are used for colouring purposes in the Northern countries. + +About 2,000 species of Lichens have been described. If we disregard the Basidiolichens, which will be considered on page 127, the remaining Lichens (Alcholiclens) may be divided into the two following orders according to the structure of the fruit-bodies: + +Order Pyrenochilenes. The ascomata (asporae) are spherical or disk-shaped, as in the Pyrenomycetes, more rarely linear (Graphites). + +According to the nature of the thallus, these Lichens may be divided into —— + +a. Thallus homomorbus, but not gelatinous, branching according to the mode of growth of the Alga: *Ephedra* (Fig. 18), with Alga of the genus *Sphaerophyllum*. + +b. Thallus homomorbus, gelatinous: *Lichina*. + +c. Thallus heteromorbus, gelatinous: *Ferraria*, *Pyrenia*: *Graphites* (Fig. 18), which may be considered as Hysterothecium with gametia; several species of *Graphites* are common on bark. + +d. Thallus homomorbus, fucinum: *Sphaerophyllum*. + +Order 2. Discomycetes. These are in the Discomycetes, have open asciocata, which, as a rule, are cupular, more rarely bucciothical (Glandonia). + +According to the nature of the thallus, these Lichens may be divided into —— + +a. Thallus homomorbus, but not gelatinous, branching according to the mode of growth of the Alga: *Ephedra* (Fig. 18), with Alga of the genus *Nucula*. + +b. Thallus homomorbus, gelatinous: *Collemis* (Fig. 128), with Alga of the genus *Nucula*. + +c. Thallus heteromorbus, gelatinous: *Ferraria* (Fig. 140), Lecidea, with asciocata open from the beginning; *Lecanora*, with asciocata, which in the beginning are closed, later on open, but with a rim formed by the thallus (Fig. 18); *Ricobosum*, whose asciocata are born on a stem formed by the thallus. + +481 + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +**Cultura** + +--- + +143 + +**ASCOLICHENES.** + +d. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina, Wall-Lichen, Fig. 141; is yellow, very frequent on tree-stems, stone-walls, etc., and on the ground; is frequent on tree-stems); *Sticta* (†, palmoanscens, Leng.; *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, Leng.). + +e. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina), *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, Leng.). + +f. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina), *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, Leng.). + +g. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina), *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, Leng.). + +h. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina), *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, Leng.). + +i. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina), *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, Leng.). + +j. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina), *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, Leng.). + +k. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina), *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, Leng.). + +l. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina), *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, Leng.). + +m. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina), *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, Leng.). + +n. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina), *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, Leng.). + +o. Thallus heteromorous, foliosum: *Parmelia* (†, saxatilis; †, parietina), *Lecanora* (†, palmaanscens, Leng.), *Peltigera*, especially on the Moss among trees; *Custodia* (†, palmaanscens, + +Figs. 145.—Uman herbae : nucarpura. [Slightly important]; Caudinæ are two kinds of thalliæs one only and leaf-like; the other erect which bears the apotheca and may be fruticose (Fig. 142), or cupulæ (Fig. 143); they grow in soil in forests and on heaths. + +W. H. +L + +Figs. 145.—Uman herbae : nucarpura. +Figs. 146.—Caudinæ pyriformia. + +144 + +**Basidiomycetes.** + +Sub-Class 2. **Basidiomycetes.** + +This sub-class embraces the most highly developed Fungi, with large "fruit-bodies," which in ordinary language we shortly term Funguses, Tondstools, or Mushrooms. + +They are distinguished from the Ascomycetes only by means of basidiospores, conidia, chlamydoconidia and oidia. The chief characteristic of this sub-class is the *basidium* (Fig. 145), i.e. the condiphore, which has a distinctive form, and bears a definite number (generally 4) of characteristically similar conidia (basidio- +spores, Fig. 145 c, d, e). + +Fig. 145.—Development of spores in *Corticium*. + +The summit of each basidium is produced generally into four +conical points (*sterigmate*, Fig. 145 b), from each of which a +basidiospore is abstracted. The basidium may be classified into +three principal groups, of which account is given in the +following table: + +1. The long, flat, and apparently divided basidia, +with lateral sterigmata and spores, found in the Uredinales (Figs. +146 D, I53), *Arionulaceae* (Fig. 100 B), and *Pilobaccae*; 2, the +spherical or ovoid basidia, with basal sterigmata, *Tremellales* (Fig. +150 c f g, I61 iii. iv.), and 3, the short, oval or cylindrical undivided +basidia of the *Antobasidiales* (Figs. 145, 163, etc.) ; the two +last have apical sterigmata and spores. + +The first two groups are the hyphate basidia (*protostomoides*), +of the *Protostomiales*; while the unisexual basidia (*anastomosis*) +of the *Dendrostomiales* are the third group. On the formation of the basidiospores, the nucleus + +A diagram showing the development of spores in Corticium. +a b c d + +**BASIDIOMYCETES.** + +145 + +of the basidium divides into four nuclei, each of which is transferred to a spore. + +In addition to the basidia, *simple conidiophores* are also found. +In the Protobasidiomycetes, the simple conidia are very generally found as accessory methods of reproduction in conjunction with the basidiospores, but less frequently in the Ascomycetous, e.g. among the *Dacrymyces*, *Tremella*, *Heterolobus* *anisocarpus*. + +The simple conidiophores vary in size, and in the number and shape of the conidia; they, however, resemble the basidia, and are distributed on early secondary branches of the mycelium. + +Finally, well-defined chlamydospores, formed in various ways, appear in the Basidiomycetes as supplementary reproductive bodies (compare p. 90). Among the Protobasidiomycetes, chlamydospores are at present only found among the Uredinales, but in various forms. In the majority of families of the Ascomycetous chlamydospores seldom occur (Fig. 193), but genuine chlamydospores seldom. + +In the same species several of the known forms of reproduction may be distinguished: + +The basidiospores are generally composed of white, branched strands, consisting of numerous felted hyphae; in some, sclerotia are found.—The great majority are saprophytes; some (particularly all the Uredinales) are parasitic. + +
Division I. of the Basidiomycetes.
+
+
Series I. Protobasidiomycetes: partly gamoparous, partly agamosporic.
+
+
a 2. *Autochthonous.*—Gamoparous.
+
+
b 2. *Autotrophici:* partly gamoparous, partly hominio- +c 2. gamoparous.
+
+
c 3. *Phragmophyta:* hemianiochoric.
+
+
d 4. *Cephalosporiaceae.*
+
+
Appendix. *Basimolochenes:* Lichen-forming basidiomycetes.
+
+
Series II. Protobasidiomycetes.
+
+To this series belong the lowest of the Basidiomycetes. The basidium is usually a tetrasporangium (Fig. 194), and is divided into four cells, either transversally or longitudinally, each division forming a stigmata which abstracts a basidiospore. The first three orders, *Uredinales*, *Auriculariacae*, and Tremel- + +146 + +BASIDIOMYCETES. + +laccae have gymnosporic fruit-bodies, while those of the Pilzähren, on the contrary, are mycosporic. + +Order I. **Uredinales** (Rusts). All the Rust-Fungi are parasites, their mycelium living in the interior of the stems and leaves of their hosts, causing red, brown, or black spots—hence their name "Rusts." + +The Rust-Fungi are mycorrhizal and deictate of a hymenium; for these reasons they are regarded as the simplest order of the Basidiomycetes. They are entirely parasitic, and their filaments, branches, and sporangia are all within the cellular spaces of its host, and often produce haustoria into the stem. The **rust** perennial should it enter a woody tissue; it may also hibernate in the rhizomes of perennial herbs and permeate the shoots springing from them, but in no majority of cases. The Rust-Fungi the myxidium has a very simple structure; chief morphological characters of the Rust-Fungi are the chlamydospores, in the more highly developed species occur in three forms, namely, the teleutos, +ecidios, and arachnoid. In the first two of these the head, are formed immediately beneath its epidermis, which is usually broken by the ripening of the spores, with the production of "rust," brown, red, or black spots. These chlamydospores which produce basidium are termed telosporioes. The spore on germination produces a trans- +cended hyphae which grow outwards from the base of the fertile +spores, "sporidia" generally four in number, are produced on +lateral stigmata. This basidio-fructification is gymnocarpic; +the baindra neither form a hymenium nor a fruit-body (only +converse), hence this fructification has a slight modification of +basidio-fructification. + +Many Rust-Fungi, in addition to basidiomycetes, have small, +unilocular conidia, "apertum," which are borne in conidi- +caea, "apertum." + +The **teleutospori** (Winter-spore) may be either unilocular or multilocular; in the majority of cases they are enclosed in a hard outer cell-wall, the exopore, which in some cases is very strongly developed; in others it is wanting. Each cell of the teleutospori has one germ-pore (a thin portion of the wall, for the protrusion of the germ-tube); in *Phragmidium* and *Gymnosporangium* there are, how- +ever, several germ-pores. The exopore of the teleutospori is +generally much larger than that of the uredosporiæ, and it is by +these than the majority of the Rust-Fungi hibernate. + +ELEIDOMYCETES, 147 + +In Gymnosporangium, two kinds of teleutospores are found (distinguished by their star and thickest or thickest). In many species of *Puccinia*, the form of the teleutospores varies very much, so that in the same layer spores have different forms, but all belong to the same genus. The teleutospores of *Endophyllum* resemble midizopores, since they are united in chains, whose cells are easily separated, and are produced in the interior of a hypha. In *Cephalosporium* the teleutospores are produced in chains, as in *Blastothrix*, and from each cell immediately produce teleutospores. The teleutospores of *Colletotrichum* and *Chrysomyxa* differ from other teleutospores in the shape of colletotrichum and chrysomyxa. + +The acidiospores (*Springo-spores*) are produced in chains which are generally enclosed in an envelope of hyphae; the peridium; the peridium enclosing the spores being termed the acidiosum. The acidiospores are unicellular, and generally of an orange colour; they are often separated by intercellular cells which wither and so die in the chain. The acidiospore is usually a rod-like body made up of minute, radially arranged rods. Generally germination proceeds immediately, the acidiospore producing a germ-tube, which develops into a mycelium bearing either uredo- or telotu-sporae. + +The acidiospores of *Rusti Fungi* were formerly considered as distinct genera. The species of *Uredinales* (Uredinales) are included under this name, with the peridium if wanted, were in part considered as *Cecus*. The acidiospores with fibrillose edge, or those of Gymnosporangium with longitudinal lamella-like spines on the surface. The species of *Cecus* (Cecus) stand out clearly; hence, acido-spicula on the Coniferae were known as *Peridermion*. + +The *teleutosporae* (Summer-spores) are unicellular and arise singly, seldom in chains (*Colletotrichum*). Their colourless, varie exopeuce bears, in the ovoidal portion, 2–8 germ-pores. In the majority, germination proceeds immediately, and a mycelium is produced at first given rise to uredosporae and afterwards to teleutosporae. + +The uredosporae-formation of *Midozporae* and *Cecus* are enclosed in an envelope, and hence resemble midae—between the uredosporae sterile, unicellular bodies are formed. + +The peridiums are spherical or pan-shaped conidiocysts, generally embedded in the substratum, and are produced before the acidiosum, before or simultaneously with the uredosporae, or before the teleutosporae. The conidia, as far as observations go, do not generally germinate under ordinary conditions. + +Among the Rust-Fungi some species are found which only form basidiomycetes and teleutosporae (*Puccinia malacocarum*, + +148 + +**DADINUMCETES** + +*Chrysogonum abietis*. Other species have in addition uredospores; others spermatangia and necidia, and others spermatangia and necidia; others spermatangia, uredospores and necidia. Those species in which all the methods of reproduction are not de- +veloped must not be considered as incomplete forms. + +As in the genus *Uromyces*, the ascus produces the basidiospores, develops the basidium; in the species, however, without necidia, it develops the uredos-form, while the uredospores are also ab- +sent; the telotexture-form. It has been established in some species of *Puccinia* and *Uromyces* that the formation of necidia can be sup- +pressed, but it is not a necessary part of the cycle of develop- +ment of the species. + +The majority of *Bust-Fungi* hibernate in the teleotexture-form. Many +species are able to hibernate in the urodo-texture-form (*Gymnosporum secundum*, +*Ustilago nuda*, *Ustilago nuda* var. *nigra*, *Ustilago nuda* var. *nigra* (Uromyces pisi), an Epichloë sporella); *Phragmidium subrubescens*, on *Iowa*; +*Eriothecium alatum*, on *Aloe aloifolia*. In *Chrysogonum abietis*, the mycelium, +developing from the ascus, produces only uredospores. + +Among the *Bust-Fungi*, with several forms of reproduction, there are about sixty whose development can only be completed by +an alternation of hosts, that is, on one host only uredo- and telotexture- +spores are produced, while the further development of the gen- +erative organs takes place on another host. The ascus and +spermatangia from its mycelium can only take place on a second +quite distinct and definite host (heterocarion or heterocarion Fungi). Those Fungi which have all their forms of reproduction on the same host are called autochthonous Fungi. These Fungi, however, +always necessary that the heterocarionous Bust-Fungi should regularly +change their hosts; for example, *Puccinia graminis* can hibernate in the urodo-form on the wild Grasses, and in the spring can dis- +tribute itself again in the same form. + +As an example of alternation of hosts both various forms of develop- +ment were considered as independent genera (*Uredina*, *Reticulina*, *Cecoria*, *Periderma*), until De Bary and Oestervold established, about the same time +(1860), that these forms are different forms of some, and paved way for the right +conception of these Fungi. + +As an example of one of the most highly developed species, +*Puccinia graminis*, the "Rust of Wheat", holds a prominent posi- +tion. Its microspores and telosporoes are produced (Fig. 140) +on Grasses (on cereals, especially Wheat, Rye, Oats, and many +wild Grasses), while the necidia and spermatangia are continued to + +RASHEHOMYCETES. 149 + +the Berberidaceae. The teliospores, developed on the Grasses, hibernate on the dried portions of their host, and in the succeeding year each of the two cells of the teliospore may develop a basidium with four basidiospores (Fig. 146 D, e). The basidiospores are distributed by the wind, and only proceed to further development on Berberis or Mahonia. The germination takes place through the epidermis of the Barberry-leaf, and forms a mycelium in its interior, the latter being indi- +cated by reddish-yellow spots on the leaf. After 10-15 days the first sporangia appear (Fig. +147 B; C, a); conidia (Fig. 147 D) and a few days later the cup-shaped oecids (Fig. 147 E, f, g, d, e). The former are generally on the upper, and the latter on the lower surface of the orange-coloured scutellum; spores scatter like dust, and germinate only on Grasses. Germination takes place in about two days when placed on any green part of a Grass. The mycelium enters the Grass-leaf through a stoma; a mycelium is de- +veloped in the leaf, giving rise to numerous chloronucleated spot (Fig. 146 A); in about 6-9 days the epidermis is ruptured over the red spot, and numerous reddish-yellow ureosporae, formed on the mycelium, are set free. The ureosporae (Fig. 146 B) are scattered by the wind, and can + +Illustration showing stages of Basidiomycete life cycle. +**Fig. 146.—Puccinia graminis.** + +A +B +C +D + +150 +RASIDIOMYCETES. + +germinate should they fall on the green portions of other Grasses ; they then emit 3-4 germ-tubes through the equatorial placod, +germinating at the base of each, and by means of these, a new mycelium is then developed, and in about eight days a fresh production of uredospores takes place, which germinate as before. +The uredospore-mycelium very soon produces, in addition, the brown, feathery, or woolly, or sometimes the yellowish brown spots, the familiar uredospores on the cereals being quite suppressed towards the close of the summer (Fig. 146 C, D). The "Run of Wheat" hibernates on some wild Grasses in the uredo- +spore-form. + +147 +Fig. 147.--Eriophyes trachydes. A Portion of lower surface of leaf of Barberry, with +chlorocarpus (axial). B Small portion of leaf, with sporangia, from above. C Transverse section of leaf, showing chlorocarpus (a) and sporangia (b), from below. D Portion of leaf, showing chlorocarpus (a) and two ripe spores (c, d), f chain of +uredoconidia. E Hyphae, from above. + +Grasses are attacked by Eriophyes trachydes, Fig. 147 has bifidaele teleutospores, each having a pore-pore, and the spores when present have an indented peridium; some spores, as exceptions, have L-shaped teleutospores. Many species are +metazoaous, for example, P. prunus, described above; P. rufus, which also infests various Grasses but whose spores appear on *Achillea*; the manner of + +A: A portion of lower surface of leaf of Barberry, with chlorocarpus (axial). +B: A small portion of leaf, with sporangia, from above. +C: A transverse section of leaf, showing chlorocarpus (a) and sporangia (b), from below. +D: A portion of leaf, showing chlorocarpus (a) and two ripe spores (c, d), f chain of uredoconidia. +E: Hyphae, from above. + +148 +Fig. 148.--Uredinae. A Uredinae. B Uredinae. C Uredinae. D Uredinae. E Uredinae. F Uredinae. G Uredinae. H Uredinae. I Uredinae. J Uredinae. K Uredinae. L Uredinae. M Uredinae. N Uredinae. O Uredinae. P Uredinae. Q Uredinae. R Uredinae. S Uredinae. T Uredinae. U Uredinae. V Uredinae. W Uredinae. X Uredinae. Y Uredinae. Z Uredinae. + +The following are the principal genera :--A Phragmidium (Fig. 148 A). This is a very common genus on grasses and other plants; it is metazoaous and has a large number of spores in each teliospore; the spores are often produced in great abundance and may be found in great numbers on the leaves or stems of the host plant; they are usually produced in clusters or chains and are often seen to be attached to the leaves by a short stalk; they are generally ellipsoidal or ovoid in shape and have a smooth or slightly roughened surface; they vary greatly in size according to their age and stage of development; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they are usually pale yellowish-brown in colour but may be greenish-yellow or even green; they are often seen to be covered with a fine downy or woolly substance; they are usually found in large numbers on the leaves or stems of the host plant; they are often seen to be attached to the leaves by a short stalk; they + +BASIDOMYCETES. +151 + +teleomorphs are small; they contain paraphyses, and are for a long time covered by the epidermis. *P. corvus*, on Oats and Rye Grass; its scidia on Rhinum; the teleomorphs are surrounded by a crown--"conocyclic processes." + +*P. coryli*, on the leaves of *Corylus* and *Rhamnus*. *P. mordax*, on *Medicago cerealis*; the medium on *Orchis*. *P. porum*, on Meadow-sweet. + +The following species of *Puccinia* have been found growing on species of *Corza*: + +*Corza* has their scidia on *Urtica*, *Equisetum*, and *Lycopodium*. + +Of those *aerotrichous* species, which have all their generations on the same plant, we have: *P. corvus*, *P. coryli*, *P. mordax*, and *P. porum*, from which they have taken their "peife" names.--As representative of the genus, we may mention: *Ustilago* (the genus of the smut), *Urodo* (the genus of the smut), and *Telosphaera* (the genus of the smut). + +The spermatophore has strong odour.--A peculiar group (*Leptopuccinia*) has only teleomorphs, which germinate immediately, and produce a mycelium with a large number of sporangia, on a number of Carpathiaceae; and *Fusarium*, in various Malouines, introduced in 1798 from South America to Europe, where it soon proved very destructive. + +*Uromyces* (Fig. 16) differs only from Puccinia in always having unicellular teleomorphs, but it is more numerous than the former, and is found at first growth below *U. pitts*, whose scidia are found on *Zephyraea cyprinoides*, and *U. dactylidis*, whose scidia are found on *Ranunculus*; to the same extent as the former. + +*Phragmidium* has teleomorphs with three cells (one below and two above), on *Spiraea albae*. + +Fungi (Fig. 16).--(10) has teleomorphs consisting of a row of cells (3-10) arranged in a straight line; the upper cell has one germ-pore and the lower four germ-pores placed equidistantly apart. The scidia are small, and have large, irregular scidia without peritrich, but often with bent, club-like paraphyses (Fig. 16 b and c); they are found on *Euphorbia*.--(11) has a similar structure. + +*Gymnosporangium* (Fig. 15).--(15) has bicellular teleomorphs collected in large, gelatinous masses on leaves of various plants; each cell is 4-gram pores are found. Uredospores are wanting. All the species are heterothecous; the teleo- +spores appear on Juniperus, the scidia (Bretella) on the Fomaceae. G. adhaer. + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromyces pitts. +a b + +Fig. 16.--Uromytes + +152 + +BASIDIOMYCETES. + +on *Juniperus communis*, J. virginiana, etc., has the ascilla (" *Rivularia concinna* ") on *Fucus comans* (Fig. 152); G. *japonicae* on *Juniperus communis* with " *Reticula corona* " (Fig. 154) on *Sorbus aucuparia*, *Aria nicaea* (s. arida) and *Mentha aquatica*. On *Salix caprea*, *Salix aurita*, *Salix caprea* belonging to it (" *Rivularia lacustris* ") on *Crataegus aculeata*. + +*Melanopus* has prismatic teleutospores placed parallel to each other and forming a chain, which is often broken into two parts, and then divided into several cells (Fig. 153). The ascilla, without perithecium, belonged to the old genus *Corma*. M. *capreosum*, on Willows, has the ascilla (*Corma congo*) on *Eucalyptus*. M. *barklyi*, on Oaks; the ascilla on *Sulze*. + + +A small diagram showing a structure with multiple branches. + + +Fig. 152.—Phycomyces gracilis: a monostome ; b and c two paraphyses; d a young teleutospore; e a teleutospore with a basifilum and two basidiospores (0), f two modes of endogamia. + +repens and *Ophioglossum*. M. *plutinosus*, on leaves of the Aron, scallion on Fine branches (Fine shoot fungus); M. populicola on *Populus simillima* and *nigra*; M. *bataurina* (Fig. 138), on Birch leaves; M. *pedicellatus* (Fig. 151), on leaves of *Fraxinus excelsior*, developing in the apical part of the stem, at the time of injury to the Finx; M. *agrimoniae*. + +*Cultoporella perspicua*: teleutospores on *Podocarpus vitifolius*; *aparoma- gothi* and *aparomatoidei* (Fig. 156). + +Calogeroidea (Fig. 155) forms its teleutospores in reddish yellow chains; for + +RASEDOSMYCETES. +153 + +the teleutosporae, see page 147. C. *arcanum*, on the Ground-leaf; its acridium (Pseudorhizum *vulgii*) on Fine-leaves (Fig. 155 e). Other species on *Sambus*, *Petasites*, *Campanula*, *Rhinanthaceae*. + +*C. *arcanum*. - On the ground-leaf red, branched teletosporae-chain; each spore develops a 4-celled basidium. C. *leuca* on *Lobium palustre* ; its acridium on the leaves of the Fig. C. *albescens* (Fig. 156), without acridio- and acridio- sporae, but with a few acridia on the leaves of the Fig. C. *albescens* (Fig. 156), without acridio- and acridio- sporae, but with a few acridia on the leaves of the Fig. + + +A small diagram showing different stages of development of a spore. + + +Fig. 151.—Teleosporae pericarp with endospores; cf. figs. 152, 153, from different nodes. +152 + + +A small diagram showing different stages of development of a spore. + + +Fig. 152.—Teleosporae *Salinae*: a endospore; b three configuratements of endospores; c four configuratements of endospores; d four configuratements of endospores with three basidiospores, (a to d). +153 + +ends are formed on the leaves, and in the following spring the real cushions of spores. + +*Crescentium* (Figs. 157, 159) has multicellular teletosporae united in numbers two to five, forming a cushion-like structure on the leaves of *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*, *Bilbe*. + +154 + +**BASIDIOMYCETES.** + + +A small leaf with three clusters of spores. +(a. ant. stel.); b three conidia; c two microspores on one of which are seen the germi-pores; +d a portion of the wall of an ascidium; e, f, two trichosporae. + + +**Fig. 104.—Gymnosporangium juniperinum : a small leaf with three clusters of spores.** +(a. ant. stel.); b three conidia; c two microspores on one of which are seen the germi-pores; +d a portion of the wall of an ascidium; e, f, two trichosporae. + + +A fine-leaf with spores (Peridermium sulfol.) set, +one 3 mm microspore; d a germinating microspore; e a chain of trichosporae; f an abortive +trichosporae of which the terminal one has germinated and produced a basidiopore. + + +**BASIDIOMYCETES.** 155 + +(Fig. 150), on which it causes great damage; c. *asciopodium*, on *Ficus* *ocellata*; its *sporidia* (*Peridermium cornei*) on the stems and branches of *Ficus* *albicaulis*. + +a b c d e f g h i j k l m n o p q r s t u v w x y z + +Fig. 150.—*Chrysoppyes alciata*: a bud of the Fig, with 4 clusters of *sporangia* (a); b, a cluster of *sporangia* (b); c, a *sporangium* (c); d, a *sporangium* (d); e, a *sporangium* (e); f, a *sporangium* (f); g, a *sporangium* (g); h, a *sporangium* (h); i, a *sporangium* (i); j, a *sporangium* (j); k, a *sporangium* (k); l, a *sporangium* (l); m, a *sporangium* (m); n, a *sporangium* (n); o, a *sporangium* (o); p, a *sporangium* (p); q, a *sporangium* (q); r, a *sporangium* (r); s, a *sporangium* (s); t, a *sporangium* (t); u, a *sporangium* (u); v, a *sporangium* (v); w, a *sporangium* (w); x, a *sporangium* (x); y, a *sporangium* (y); z, a *sporangium* (z). + +To the Fungi of which the acidulum is known, whilst the remaining forms are still undetermined, but which are without doubt heterotrophic, belong *Eudidium*, with long slender hyphae; and the short club-shaped swellings on stems and branches of *Albizia alba*, and *Eudidium stracheyi*, (Fig. 168), which attacks Fig-trees. + +Order 2. **Auriculariae.** + +The long, transversely divided basidion bear internally 4 long hyphae with basidiosporae. + +(Fig. 109.) The basidiosporae are arranged to form an hymenium on the surface of the fruit-body. +Parasites or saprophytes. + +a b c d e f g h i j k l m n o p q r s t u v w x y z + +Fig. 151.—*Eudidium stracheyi*: a scale of costa of Figus alba; with numerous metidia ; b, metidia surrounded by a series ; c, cell of the peridium. + +Order 3. **Pucciniales.** + +The spores are produced in large numbers in the form of conidiophores or conidiophores with conidia. + +(Fig. 169.) The conidiophores are usually cylindrical or slightly curved; they are often branched at their base. + +The conidia are generally ellipsoid or oblong; they are often covered with spines or other projections. + +The conidiophores may be solitary or in groups; they may be free or attached to the stem of the plant. + +The conidia may be produced singly or in chains; they may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced by budding or by division. + +The conidia may be produced + +156 + +RASDIOHETEROCYTES. + +*Anisocarina semilucens* (Anisocar *judei*). *Jutard-ear*, has large fruit-bodies, which may attain the size of several inches, resembling an ear or a mussel shell. In the moist condition they are flat-basal, tough, and glabrous; but when dried, becoming hard and brittle. The exterior is covered with short hairs, while the internal surface bears the hymenium. *Bambus* domus is a branch of old Elder-trees (Sambucus). + +Order 3. Tremellaceae. The round, pararhodoid, longitudinally divided basidium bear 4 elongated sterigmata, situated apically, and 4 inconspicuous sporangia (Fig. 100 C, D), and are found in the interior of the fruit-body. The fruit-bodies are frequently glabrous and quivering; similar fruit-bodies also found in the *Dichomycetes* and *Fungi Imperfecti*. Simple basidiospores, which appear not unfrequently in the basidiocarps, before the basidia, are known in many species. Saprophytes. + +*Exidia* has kidney-shaped, oblong basidiocarps, on wood—*Orocutella* has conic basidiocarps, on wood—*Dendrione*, etc., on wood—*Orocutella* has conidiocarps; *C. crevis* on Cherry-wood—*Selatina terracina* ; the yellow. + +For 108.—Fredericium erectum; *A. semilucens* (nat. size). + +4 + +Fig. 100.—*Anisocarina semilucens*: a–d basidium to vari- +ous stages of development; e–g sterigmata; h–k spore. +a–d Basidium to various stages of development; e–g +sterigmata with basidiocarps (*x 200); d Basidium to +various stages of development; e–g Sterigmata with +basidiocarps (*x 200); f Basidium to various stages +of development; g Sterigmata with basidiocarps (*x +200); h Basidium to various stages of develop- +ment; i Sterigmata with basidiocarps (*x 200). +e Sterigmata with basidiocarps (*x 200); f Basidium +to various stages of development; g Sterigmata with +basidiocarps (*x 200); h Basidium to various stages +of development; i Sterigmata with basidiocarps (*x +200). +j Sterigmata with basidiocarps (*x 200); k Basidium +to various stages of development; l Sterigmata with +basidiocarps (*x 200). + +**BASIDIOMYCETES.** 157 + +folded, quivering, orange fruit-bodies, about one inch in breadth ; *T. lutucens* (Fig. 161) has orange-yellow conidia; and yellow basidial-layers; *T. frondosa* has fruit-bodies upwards of a foot in breadth. + +Order 4. *Pilariaceae.* The transversely divided basidia have no sterigmata, but sessile basidiospores, and fill up the cavity of a closed (conidiophore), or are as a globus without a regular arrangement (hymenium wanting). + +*Filaria fagi* on the old stems of the Copper Beech : *P. petrari*, on dried branches of the Hornbeam, has stalked, exstipulate fruit-bodies. + +Fig. 161.—From *Cultorum* I. and II. fruit-bodies (first story); III. terminal portion through a fruit-body; 5 basidia ; 6 conidia; IV-VI basidia; VII basidiocarp with a second germ; VIII a basidiocarp with yonosporic budding (conidiospore); IX a conidio- carpus (III-IX basidiospores). + +Series 2. *Autobasidiomycetes.* + +This second and larger part of the Basidiomycetes is characterised by its more highly developed structure, by its club-shaped, or cylindrical basidia, which generally bear 4 ( seldom 2, 6, 8 ) spionially placed sterigmata and basidiospores (Fig. 145). The fruit-bodies are partly gymnosporic (in the first 3 orders and in some Agaricae), partly hemiptycosporic (in orders 3-6 of the Hymenomycetes + +158 +BASIDIOMYCETES. +and in the Phalloidae, the fruit-bodies in these orders are in the young conditions more or less anisocarpic, but later on generally open below and bear the hymenium on the under surface of the fruit-body), partly also anisocarpic (in the Gasteromycetes). + +Doroporella dilopsocera : I fruit-body (nat. size); II vertical section through the hymenium; III vertical section through the stipe; IV to VII chains of spores more or less strongly magnified; VIII basidiomata of D. impropria ; IX germinating basidiomata of D. impropria ; X 2 basidia with basidiospores (higher magnified); XI Doroporella plessoides (nat. size). + +I +II +III +IV +V +VI +VII +VIII +IX +X +XI + +ELSIDIOHYCETES. +159 + +Family 1. Dacrymycetes. + +The long, club-shaped basidium bear two tapering sterigmata, which develop remarkably large basidiocarps (Fig. 162 II, XI) and form gynomycetous fruit-bodies with hymenium. order 1: Ophioglossum Dacrymycetes. This order includes 4 genera of which the first two develop the hymenium on the whole surface of the fruit-body, but the last two only on its apex. + +Dacrymyces: the folioid, gelatinous, Tremella-like fruit-bodies break out in winter and spring from the leafy stems of the host-plant, Vulpia. D. delicens is very common (Fig. 121). The following genera have cartilaginous fruit-bodies: Calonectria (Fig. 120), with club-like, simple, or branched, Clavaria-like stipe; and Gastrodia (Fig. 123), with a short, thickened stipe, constricted together on the wood of Coniferus. Gastrodia resembles a Porina, and has the hymenium only on the lower upper surface. Dacrymyces resembles a Mit- +rata (Fig. 182). + +Family 2. Hymenomycetes. + +This family is very rich in species (more than 8000 have been described), and to it belong all the "Mushrooms" and "Toadstools." + +The fruit-bodies present very various forms; they are generally fleshy, but some are thin and fragile, and others are woody; some are often perennial. The basidia are more or less equidimensional and bear generally 4 ( seldom 2, 6 or 8) sterigmata and basidiospores. The hymenium in the fully-formed fruit-bodies lies free on the surface of the stipe or on a stalk, and is usually attached to the commencement exposed; fruit-bodies gynomycetous; orders 3-6 have hemianthocarpic fruit-bodies (p. 157). In the first order the basidia (or the hymenium) are developed immediately from the mycelium; in the second order they appear after a certain period of higher grade of development, and have between the mycelium and hymenium a special hyphal-lamina, a struma, which is cutaneous, club-like, or cornoidal, etc., and in general bears the hymenium on the surface of the stipe; in the third order the forms most highly developed (orders 4-6) a new tissue—the hyphal lamina—is introduced between the struma and hymenium, which appears on the under side of the fruit-body in the form of warts, projections, tubules, etc.; this tissue is often very conspicuous (Figs. 160a, b, 174). These structures are frequently found in the hymenium among the basidia. In the Hymenomycetes few examples of ovidae can be recognised at first. More frequently chlorenchyma are found, particularly ocella. + +The ocellus is richly branched, generally colourless, often peren- +nial; it lives in humus or decaying wood, and is solanum pas- +taceum. + +160 + +RHIZOMORPHACEAE + +The hyphae generally have clamp-connections and unite, sometimes, to form a rhizomorpha (Fig. 177) or solerotia with coloured, pseudoparenchymatous covering. + + +A diagram showing the structure of a rhizomorpha. + + +Fig. 188.—Benditrichum vanneff. 1 Hypertrophied stem of *Funiculus* volv. (Fig. 1.) Inflorescence with a rhizomorpha (Fig. 2.). 3 Solerotia with rhizomorpha (Fig. 3.). 4 Solerotia with pseudoparenchymatous cells; p hypodermal cuticle; e epidermis with basidiole in various stages of development; b basidioles in solerotia with germinating spores. VI. and VII. spores germinating in water (IV-VII x 250). + +**EASIDOMYCETES.** + +**Order 1. **Tomentellaceae.** To this order belong the simplest of the Hymenomycetes. The basidia (Fig. 145) arise free and irregularly from the mycelium; a hymenium is entirely absent or very slightly formed (in *Corilis* it attains its highest development); fructifications are usually sessile, but may be on stalks; mem- braneous or leathery coverings on bark and wood. Some are parasitic. + +*Hyphomyces* without conidia. - *Tomentellus* with conidiophores; growing on wood or bark. - *Eumycetes* (Figs. 146, 147). - *Hypocrea*, *Corticius*, *Arthrobotrys*, and *Rhodendron*, forms flaky-porous, white, or red coverings and may cause hyperthropy of the parts attacked. *E. wangiarii* is parasitic on *Picea*. - *Corticius* (Fig. 148), a large genus of *Corilis* resembling as long as a finger, which formerly were regarded as aerial roots... *Corilis* form membranous to leathery leaves or crusts; *C. quercusum* on wood not yet known; *C. corymbosus* on bark; *C. rhodendricum* has a blue hymenium; *C. giganteum* on the bark of fallen Pine-trees. + +**Order 2. **Clavariaceae.** The hymenium is situated on a stroma, and either completely covers the smooth surface of the more or less flat gymnocarpic fruit-body, or is developed only at one side, usually well defined upper portion of it (Fig. 274). Paraphyses absent. The vertical, white, yellow, or red fructifications are erect, unbranched, or unbranched or richly branched (Fig. 125). Generally on the ground in woods, seldom on trees. + +**Genus :** Clavaria, generally large Fungi with thick, round cushions. C. bergaria has a very thickened cushion-like body, with short, flesh-coloured branches; *C. lutea* has a brittle, richly-branched fruit-body (Fig. 121); *kastelia* with two large spores. *C. parvispora* consists of a single, unbranched club of a yellowish colour with a few short branches; *C. aurantiaca* has a yellowish fruit-body as large as a white cabbage-head, with an agreeable taste... *Typhula* and *Pistillaria* are small Fungi with filamentsous stalks, terminating in a small head; the stalks of the former often arise from a small, apicaloid scerotium; the latter is distinguished by its branch bearing only two spores. + +Fig. 104.—Clavaria cretacea (nat., size). + +162 + +**BASIDIOMYCETES.** + +**Order 3. Thelephoraceae.** The hymenium is placed on a stroma and covers the smooth surface of the leathery hymenio- +carpic fruit-body, generally on its under side. The edge of the stroma, which bounds the hymenium is sometimes especially developed. + +**Genus: Thelephora.** The fruit-bodies in this genus are brown, very ir- +regularly shaped, and often hollow. The species too are brown, but in the other genera they are white or yellowish. **T. lanuginosa** (Fig. 165) is imbricant, semi-circular, dark-brown pinnis, which is jagged at the edge and upper surface. The fruit-bodies are very often raised above the ground by means of a short stalk. **S. purpurea** (Fig. 166) is a strong young seedling by growing above and smoothing them...Streptos has a stiffer fruit-body, with a distinct,坚韧, internodular layer. It grows on hard wood and is brown to blackish-brown in colour; its free edge is provided with a number of stout hairs, the upper surface being divided into a number of zones. **S. purpurea** has a red-violet hymenium and is found on dead wood. **C. ophiophila** has a previous species...Ophiophila has a brownish fruit-body, often borne on a stalk, the con cave surface being covered with long hairs. **C. coriacea** has small, white Fungi, growing on Moss and dead stem...Solenia is similar to Streptos but the fruit-bodies are smaller and hairy; they are found clustered together or scattered on dead wood... **Craterellus** has a brownish fruit-body, often borne on dead wood. **Coriolus** is shaped like a trumpet or a "horn of plenty". It is dark-green, several inches in height, and grows on mosses and ferns found in forests. It is distinguished by the basidium bearing only two sterigmata. + +**Order 4. Hydnaceae.** The fruit-body is most frequently fleshy, and varies considerably in shape; the simplest forms being conoporate or high conical. The Asymptoma is formed by the free downward-turned surface of the stroma, which takes the form of soft emergences hanging vertically downwards. The emergences may be thorny, awl-, or wart-like. The species are found growing on the soil and on dead wood. + +**Genus: Hydnoceraea.** The fruit-body is brownish-yellow. **H. repens** is yellow, the stalk being placed in the centre of the pileus. It is an edible + +1 In the repentate fruit-bodies a fertile and sterile surface cannot be distinguished (cf. Polyporeaceae and some Stereom-species). + +**BASIDIOMYCETES** + +163 + +species, and often forms "fairy rings" in woods. *H. marcescens* (Fig. 161) is dark-brown, with stink placed at the edge of the pithus. It grows on old Pterospermum, and is found in the tropics. *H. erinaceus* grows on old tree-trunks. The fruit-body is yellow and very large, with a long stalk, and a broad, flat cap, which may be 5 inches in length. --Ipecac has a leathery fruit-body, partly resupinate, partly with free, projecting edge; the under side bears tooth-like emergencies which are arranged in groups of three, and are connected by a network of veins, partly resupinate, with radially-arranged folds on the free side, and persistent border. + + +A small illustration showing different stages of development. + + +Fig. 168.--Hydnum marcescens, upon a firewood, in different stages of development. + +Order 5. Polyporaceae (Pore-Fungi). An order very rich in species (about 2500 species are described). The fruit-body is of very different forms--resupinate, projecting like a basket, hoof-like, or umbrella-shaped. In some it is fleshy and edible, in others leathery and very persistent on the wood. The hymenophore is situated on the under side of the fruit-body, and consists of wide or narrow tubes or pores, whose inner surface is clothed with the hymenium (Fig. 167). In some fruit-bodies large cavities are formed between the tubes or pores, and these interlace with the labyrinthine curved and reticulate folds. Many hymenopores are known in some species. Conidia occur very rarely. Many species work considerable damage : such as parasitise on trees, others by destroying timber. + +*Gymnosporangium*. *Polyporus* (Pore-Fungus). The tubes are narrow, accurately fitted together, and forming a thick layer on the under side of the fruit-body, appearing + +164 + +RASIDIOMYCETES. + +as a number of fine holes. The fruit-body most frequently resembles a bracket, or a hood-chape, with one side upwards (fig. 107). It is very often per- +ennial, and a new layer of tubes arises in each succeeding period of vegetation. +Stroma, corresponding to the periodically interrupted growth, are thus formed in +stages, and the fruit-body is composed of several such stromata. The fruit- +body, as well as in the interior, as a series of concentric belts, sometimes as +many as ten, are more or less covered with long, slender, white filaments, +especially the Rhizomorphs (touwoudh) which arise from the base of the stalked +branches, and the hyphae, following the course of the modulatory rays, find their way into the stroma. The latter is usually conical in shape, and extends downwards, and perpendicularly, so that the wood becomes rotten (wh-ir-not). +and thick filts of mycelium are formed in radial and tangential directions. A + +The stroma consists of the +youngest parts of the hy- +plus containing a brown +mycelium, and a yellow +mycelium between the rotion +and the unmarked parts of +the stroma. In this place where the mycelium grows outwards, +the cambium becomes de- +stroyed and further growth +is arrested. Long peri- +tinal furrows arise on the +stem. It is at these +places where the heart- +shaped, ash-coloured +fruit-bodies are developed, +which are attached to the + circumference of uplands of +the root. The interior of +the stem is filled with a +dried-up, loosely held, +white mycelium, which is +which has been used for +timber and as a stylophore. +The fruit-body (fig. 108). +F. gatunensis has a broader, +dark-brown, more rounded +fruit-body than P. fusaceus in a +similar manner, but +wood of which becomes +rotten. The fruit-body is found on the stems of Funa, causes a kind of "red-rot" in the stem. F. fusaceus has its own specific name (rhubrid), is produced not in Oaks and Apple- +trees, but in Fagus silvatica L., and in Quercus robur L., and grows on Larch-trees in the south-east of Europe. P. reticulare has thin, semicircular + +Fig. 107.--Polyporus sparsus. Section through the middle part of a young fruit-body showing the tubes, formed by irregularly foliated hyphae, many of which have become detached from the tube wall and cover the walls of the tubes, and from which the tendrils with the spores proceed. + +![Image](image-url) + +**Note:** This image appears to be a section through a young fruit-body of Polyporus sparsus (commonly known as "Puffball"), showing the tubes formed by irregularly foliated hyphae, many of which have become detached from the tube wall and cover the walls of the tubes. The tendrils with spores proceed from these tubes. + +**Description:** + +- **Fruit-body:** The fruit-body most frequently resembles a bracket or a hood-chape. +- **Perennial:** It is very often perennial. +- **New Layer:** A new layer of tubes arises in each succeeding period of vegetation. +- **Stroma:** Corresponding to the periodically interrupted growth, several such stromata are formed in stages. +- **Structure:** The fruit-body is composed of several such stromata. +- **Interior:** The interior is usually conical in shape and extends downwards and perpendicularly. +- **Mycelium:** Thick filts of mycelium are formed in radial and tangential directions. +- **Stroma:** Consists of young parts of hyplus containing brown mycelium and yellow mycelium between rotion and unmarked parts of stroma. +- **Heart-shaped Fruit-Bodies:** Found at places where mycelium grows outwards. +- **Cambium:** Becomes destroyed and further growth is arrested. +- **Peritinal Furrows:** Arise on stem. +- **Interior:** Interior filled with dried-up, loosely held white mycelium. +- **Use:** Used for timber and as a stylophore. +- **Fruit-body (fig. 108):** Heart-shaped, ash-coloured fruit-body attached to circumference of uplands of root. +- **Wood Rot:** Wood becomes rotten. +- **Specific Name:** Fagus silvatica L., Quercus robur L., Larch-trees. +- **Other Species:** P. reticulare has thin semicircular fruit-body. + +**Additional Notes:** + +- **Rhubrid:** Specific name for Fagus silvatica L., Quercus robur L., Larch-trees. +- **Fagus Silvatica L.:** Commonly known as "Beech". +- **Quercus Robur L.:** Commonly known as "Cherry". + +**BASIDIOMYCETES** + +frank-holin, with zones of various colours on the upper side; it is one of the most frequent species on tree-stumps. *P. frondosus* grown on soil in woods, and consists of numerous aggregated fruit-bodies, which become very large and fleshy, and are often found in great numbers. The fruit-body is soft; it is very leathery, with central stalk, and has concentric zones on the upper surface of the fruit-body. *P. saporiarius* destroys the wood of living Firs (Picea excelsa). + +Fir (Picea excelsa), causing it to become reddish-brown. + +This Fungus enmeses "wood-rotters" by a "diapause." *P. saporiarius* destroys many trees in woods, and is also very destructive to Limes and Thorns, and is known under the name of "white-rot" by A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. A. + +Asterobolides anu- +nium (Polygona anu- +nium, Trametes radicil- +laria), is a Fungus charac- +terized by its Agaric-like com- +plexity, and is a parasite on the Fir, Fir, Birch, Beech, etc. + +Fig., 108.--Base of a Fir-tree, with a number of fruit-bodies of *Heterobolides anu- +nium*, growing on the bark, indicated by the dotted line (fig., nat., scale). + +Fig., 173.--A fully developed fruit-body of *Nigropus poid* (Trametes poid), lateral view (nat., scale). + +A diagram showing the base of a Fir-tree with fruit-bodies of *Heterobolides anu-nium* growing on the bark. +A diagram showing a fully developed fruit-body of *Nigropus poid* (Trametes poid) from the side. + +165 + +**RASDIOHYCETES** + +and in the chief cause of a root-disease (red-rot) in Trees and Firs; the fruit- +bodies develop a large number of basidiocarps; they may be very large and are found just beneath the surface of the soil (on living or dead roots), and exposed to the air, or in the soil, and are often seen on the surface of the ground. + +**Phylogaster** has cushion-like fruit-bodies, which consist chiefly of chlamy- +dospore-chains, formed of ellipsoidal spores, which alternate with short hyphae forming a network. The fruit-bodies are usually sessile, but sometimes they are free, but limited to a small group of tubes. *Ft.* alba (*Phylogaster nattelispatha*) grows on stumps of Coniferae and forms irregular cimae, at first white and later on brown, when dry. + +*Botrytis* (Fig. 17) has a fluffy fruit-body resembling a common Mushroom, with central stalks. The layer of tubes is easily detached from the plums, and the fine tubes are easily separated from each other by hand, and from wood. *Gilliate species are:* *E. cutis*, with thick, reticulate stalk; *E. scaber*, with thin stalk and fine plum; *E. arvensis*, with long, thin stalks. In some species the tubes have red openings, and the last turns quite black. *F. nattelispatha* (see Fig. 18). *F. nattelispatha* (dead-stem Fungus), has a red, fluffy, edible fruit-body, with red juice. The tubes are long and thin, and can also be developed. Grown on old Oaks. + +*Hymenomycetes ("Dry-rot")" has a rem- +nant of the stem of the plant remaining intact, and the remaining portions covered by reticulate, ramified veils of a rust-colour. In favou- +rable weather conditions it flourishes under large drops of water—hence its specific name "natura". The outer veil is yellowish, +yellow at first colouring, and then yellow; +when dry it is tough and leathery. It +develops on dead wood and over boards and beams and even over the masonry, giving rise to a disagreeable smell. +The fruit-bodies are small and grow on the roots of plants. + +Fungus lives on Fine- stems. +It is brought from the forest on thelags of timber, +and is detached from bark by the mycelium and the basidiocarps. +The living mycelium is white or greyish-white, with long branches. The basidiocarps are often ejected a distance of a metre; they are elliptical or ovoid-shaped, with a short stalk. They are found in wood, +or in fruit-juice which has been neutralized with urine or alkaline chemoanates. + +*Indulata* (Lathyriinum Fungus), has bracket-like, early fruit-bodies with irregu- +larly folded tubes; these are often covered by a transition to the Agaricaceae. +*G. verrucosa* is frequent on Oak-stumps. + +Order 6. *Agaricales* (Mushrooms, *Candlstoilea*). The hymenophore consists of knife-like plates (*lamella*, *pille*), which are situated on the under side of the umbrella-like pinnus of the fruit- + +Fan 371—Botrytis nattelispatha + +This fungus causes a red-rot in conifers +a portion of the plums. + +Fungus lives on Fine-stems. +It is brought from the forest on the lags of timber, +and is detached from bark by the mycelium and the basidiocarps. +The living mycelium is white or greyish-white, with long branches. The basidiocarps are often ejected a distance of a metre; they are elliptical or ovoid-shaped, with a short stalk. They are found in wood, +or in fruit-juice which has been neutralized with urine or alkaline chemoanates. + +*Indulata* (Lathyriinum Fungus), has bracket-like, early fruit-bodies with irregu- +larly folded tubes; these are often covered by a transition to the Agaricaceae. +*G. verrucosa* is frequent on Oak-stumps. + +Order 6. *Agaricales* (Mushrooms, *Candlstoilea*). The hymenophore consists of knife-like plates (*lamella*, *pille*), which are situated on the under side of the umbrella-like pinnus of the fruit- + +RASIDIOMYCETES. +167 + +body; and radiate from the central stalk. Those which are first formed extend from the edge of the pileus to the stalk; those formed later reach only a longer or shorter portion of this distance, according to their age. In structure the lamellae (Fig. 174) consist of two layers, viz., the hymenium, which covers the hyphae of the pileus; these terminate in a layer of shorter cells, the *anamorph* layer, immediately beneath the hymenium which is composed of basidia and paraphyses. In a few species, but not in the majority, the lamellae are branched, and in some they are decurrent; in others they have the stalk placed eccentrically, or it may be entirely absent. + + +A diagram showing the development of Pezizumyces compostae: a, b, c, d show the various stages of the development of the fruit-body. The young fruit-body is enclosed by a thin veil-like body in a somewhat later stage, slightly magnified / longitudinal section of e, a fruit forma- +tion of a more advanced stage, showing a more advanced fruit-body (dark side); / +the hymenium ; / a veiled partition (see also Fig. 180). + + +In the early stages of its development the fruit-body is more or less enclosed in a hyphal tissue—the "veil" (vedum unicucurale, or edax). The veil at first completely encloses the young fruit-body, but as it grows older it becomes torn away from the margin at the base of the stalk as the "shroud" (vesculum teforae); and part on the pileus as scales or warts. In the "Fly Mushroom" (Anamista micaeria) the remains of the veil are especially con- + +**Fig. 172.—Development of Pezizumyces compostae: a, b, c, d show the various stages of the development of the fruit-body. The young fruit-body is enclosed by a thin veil-like body in a somewhat later stage, slightly magnified / longitudinal section of e, a fruit formation of a more advanced stage, showing a more advanced fruit-body (dark side); / the hymenium ; / a veiled partition (see also Fig. 180).** + +108 +BASIDIOMYCETES. + +spicuous as white patches on the bright red ground of the upper surface of the pileus, and as a sheath at the base of the stipe (Fig. +178 a.). Another veil—the velum partiale—a hyphal tissue (Figs. +178 a; 175) stretches from the edge of the pileus to the stalk, and +enloses the lamellae. This veil is ruptured as the pileus expands, +and persists as a thin membrane on the upper side of the stipe +(annulus superius) (Figs. 173, 178 a.), or a part attached to the +pileus hanging down as a fringe round its edge.—Some genera +have no veil, but under side of the pileus being exposed from the +first (gymnosporic Agaricines). Those which have a veil (fem- +togloecarpic Agerines) afford a transition to the non-gloecaric Gasteromycetes. + +The mycelium mostly grows in soils rich in humus or dung, on +decaying trees and similar objects. Many species, e.g. *Tricholoma +pernominatum* and *Marasmius oreades*, form the so-called " fairy-rings." +The fruit-bodies in these species are confined to a larger or smaller +surface, and are arranged in a circle around a central point. The +reason for this is found in the radial growth of the mycelium, so that +the oldest portion, or the starting point, is found at the centre of +the ring, while new fruit-bodies are formed at the circumference. +The older hypha gradually die, and +at the same time, the radial growth continuing, the ring of fruit- +bodies becomes larger and larger. The " fairy-rings" are marked + +Fig. 173.—The cultivated Mushroom (Paxillus campestris). + +The mycelium mostly grows in soils rich in humus or dung, on +decaying trees and similar objects. Many species, e.g. *Tricholoma +pernominatum* and *Marasmius oreades*, form the so-called " fairy-rings." +The fruit-bodies in these species are confined to a larger or smaller +surface, and are arranged in a circle around a central point. The +reason for this is found in the radial growth of the mycelium, so that +the oldest portion, or the starting point, is found at the centre of +the ring, while new fruit-bodies are formed at the circumference. +The older hypha gradually die, and +at the same time, the radial growth continuing, the ring of fruit- +bodies becomes larger and larger. The " fairy-rings" are marked + +**BASIDIOMYCETES.** + +not only by the fruit-bodies, but also by the more vigorous growth and darker colour of the grass upon these spots. + +Some species are parasitic. An example is presented by *Armillaria* mellea, a remarkable and very destructive Fungus in woods and forests. It grows on dead wood, and is often found in great quantities, it has also black, or black-brown, horny, root-like mycelium-strands (rhizomorphs) which were formerly considered to be a special genus of Fungi described under the name of *Hymenochaete*. The mycelium lives parasitically on the roots of trees, ferns and other trees, forcing its hyphae into the bark of the tree, and then into the bark and wood, and thence penetrating into the sap of the tree. The tree is very severely at- +tacked. It may also be attacked by clusters of fruit-bodies are often found on old stumps of trees, on old timber, and in the roots of trees. The rhizomorphs, living un- +derground, can extend themselves far into the ten- +tacles and infect the roots of neighbouring trees. In this way the diseases known as "Harzatosis" and "Fellinosis," which are very destruc- +tive to young trees. + +The chief charac- +teristics by which the numerous genera are distinguished are: +the presence or absence of the two kinds of veils, the nature of the fruit-body, the form, branching of the lamella, and their position and relation with respect to the stem, the shape of the + +Fig. 374.--Puccinia morrhuae. A. Transverse section of pith showing lamella (i). B. Portion of gill more highly magnified than in A. C. Portion of gill showing lamella (ii), a sub-hymenial layer. D. A portion of the same more highly magnified than in C. E. A portion of a stage in the union highly magnified than in D. F. A portion of a stage in the union showing lamella (iii), a paraphysae. + +109 + +170 +BASIDIOMYCETES. + +pileus, the colour of the spores, etc., etc. A knowledge of the colour may be obtained by placing the pileus with the lamelle turned downwards on a piece of white or coloured paper, so that the spores fall upon it, and are collected on the paper, and the arrangement of the lamelle can then be clearly seen. + +Fig. 126.--*Pleurotus* *officinalis* (L. ed.), *Hart.:* a stem of a *P.*; b *Stemonopus-stromba:* by means of which the *P.* grows in four different stages of development. + +For 175.--*Cordyceps* *elliptica* (see page 3). + +A mushroom with a long stem and a cap with gills underneath. + +Fig. 177.--The *erythra* of *Amanita* *viola* ("Boltenia") (nat. size). + +**BASIDIOMYCETES.** 171 + +About 4,000 species belonging to this order have been described. +On account of the large number of species the order is divided into several sections. + +1. Agaricinæ: fruit-body fleshy; lamellæ membranous, knife-like, with sharp edge; basidia crowded together. The following have white spores— +*Anemita (Fly Mushroom)*, with volva, and generally also the upper ring on the stipe; *Lepista* (White Stinkhorn), with a long, bright red pilus with white spots; *A. pastinaceæ* and *A. phasidicæ*, &c. carnea is edible. +—Legume process (Fumaria Fumaria is one of the largest Mushrooms; it has a short, yellowish stem and a broad, flat cap; the spores are blackish and elongated above (Fig. 176, 177).—*Pholiota*, lamella inflated near the stalk; &c., gem- +mata, *P. subglandulosa*. *P. subglandulosa* belongs to the best of edible Fungi; *P. peronospora* +(see above)—*Clitocybe*, lamella with a white ring at the base; *Scleroderma* +(*Scleroderma* is a genus of large, brownish mushrooms); *Scutellaria*, *Scutellaria* +(*Scutellaria* is a genus of large, brownish mushrooms); *Mycena*, species numer- +ous—*Tricholoma*, species numerous—*Agaricus*, species numerous— +*Agaricus* (Fig. 178)—*Agaricus* (Fig. 179)—*Agaricus* (Fig. 180)—*Agaricus* +(*Agaricus*) (Fig. 181)—*Agaricus* (Fig. 182)—*Agaricus* (Fig. 183)—*Agaricus* +(*Agaricus*) (Fig. 184)—*Agaricus* (Fig. 185)—*Agaricus* (Fig. 186)—*Agaricus* +(*Agaricus*) (Fig. 187)—*Agaricus* (Fig. 188)—*Agaricus* (Fig. 189)—*Agaricus* +(*Agaricus*) (Fig. 190)—*Agaricus* (Fig. 191)—*Agaricus* (Fig. 192)—*Agaricus* +(*Agaricus*) (Fig. 193)—*Agaricus* (Fig. 194)—*Agaricus* (Fig. 195)—*Agaricus* +(*Agaricus*) (Fig. 196)—*Agaricus* (Fig. 197)—*Agaricus* (Fig. 198)—*Agaricus* +(*Agaricus*) (Fig. 199)—*Agaricus* (Fig. 200)—*Agaricus* (Fig. 201)—*Agaricus* +(*Agaricus*) (Fig. 202)—*Agaricus* (Fig. 203)—*Agaricus* (Fig. 204)—*Agaricus* +(*Agaricus*) (Fig. 205)—*Agaricus* (Fig. 206)—*Agaricus* (Fig. 207)—*Agaricus* +(*Agaricus*) (Fig. 208)—*Agaricus* (Fig. 209)—*Agaricus* (Fig. 210)—*Agaricus* +(*Agaricus*) (Fig. 211)—*Agaricus* (Fig. 212)—*Agaricus* (Fig. 213)—*Agaricus* +(*Agaricus*) (Fig. 214)—*Agaricus* (Fig. 215)—*Agaricus* (Fig. 216)—*Agaricus* +(*Agaricus*) (Fig. 217)—*Agaricus* (Fig. 218)—*Agaricus* (Fig. 219)—*Agaricus* +(*Agaricus*) (Fig. 220)—*Agaricus* (Fig. 221)—*Agaricus* (Fig. 222)— +edible Mushroom (Fig. +The following are white, button-like and chocolate-colored lamella lamella; it is cultivated for the sake of the fine flavor.—Spores Black: Cypriotumus +2. Marmelatæ: Fruit-body tough, almost leathery, and persistent; spores white, without ornamentation; often used as a seasoning in food.—Panna stipitifera with eccentrically placed stalks, in clusters on tree-stumps.—Schizopilus has the edge of the mushroom cut off by a ring of cells which remains visible.—Leucosporus affords a transition to *Dendalia among the Polyporaceæ.* +Rumuletæ: Fruit-body fleshy and fragile, in which two different systems of hyphae are combined; in which the spores are white or black; they are poisonous.—Rumula has generally fragile and thick lamella reaching from stalk to edge of pilus; piths frequently red.—Lactarius has white or yellow + +172 +BASEDOMYCETES. + +milky juice, which often is very acid. *L. delicious* has red-yellow milky juice, and is of a pleasant flavour. *L. hirsutum* is poisonous. + +*Hygrophorus camphoratus*. The fruit-bodies are usually solitary; sporae white. Many species of Hygrophorus have brightly-coloured pileus and grow among the grass on meadows and commons.—Nutricula is parasitic on larger Toad- +stools. It produces a peculiarly formed formation of chlamydospores, while the basidiospores are little developed. + +*Coprinus*. Fruit-bodies very nice, quite uniformly black, and are often found in groups, sometimes from one another by para- +physes. Coprinus has colourless spores, grown on manure, and sometimes developing into a mycelium. + +*Paxillus*. Fruit-body black; lamellae easily detached from the pleura and reluctantly joined near the stalk. They form a connecting link between the +Agaricaceae and the Boletaceae. + +*Cantharellus*. Lamellae reduced to dichotomously-divided folia, decor- +rent on the stalk. Cantharellus rufescens (Fig. 173) is yellow-yolk, and grows on the ground in woods (obsc.). It is allied to *Cortinarius*. + +Family 3. Phalloideae. + +The fruit-bodies before they are ripe are spherical or ovoid, and enclosed by a flesh covering, the peridium, which is perforated at maturity and remains as a sheath (Fig. 174); the fruit-bodies are hermaphrodite. + +Order 1. Phallaceæ (Stink-horns). The peridium has a complicated structure and is composed of three layers, the in- +termediate one being thick and gelatinous. The gleba (the tissue which becomes gelatinous when the fruit-body is mature), which expands into a primary stalk and by its sudden distension, rupturing the peridium, elevates the gleba and hymenium above the peridium, which remains as a sheath. The gleba becomes gelatinous and finally drops to the ground. To this order belong many +peculiar and often brightly coloured forms, which are natives of the Southern Hemisphere. + +*Phallus impudicus* (Stink-horn) (Fig. 175). has a frutic-like body which at first is +white, heavy, and soft, and resembles a hen's egg in shape and size. The peri- +dium is divided into two parts: an outer layer of thin cells and an inner one thick and gelatinous; each of these has again a laminated structure. The peridium when ruptured re- +mains as a sheath round the gleba. The gleba is large, thick, and strongly compressed (a) but afterwards expands into a long stalk (b) which bears the common gleba (c). Prior to the rupture of the peridium the gleba contains an air-space which serves to keep it free from water; this space serves to retain air films, by whose agency the spores are distributed. It is found commonly in hedgerows and in woods, growing on the ground. The much + +6 + +**HARDYOMYCETES.** + +173 + +similar and less common *P. conicus* is found on rotten tree-stumps. —In +*Clitostoma concinellus* the peridium is a thin, bright red, reticulate struc- +ture. A native of the South of Europe. *Cotula*, *Aureol*, *Mimozymes*. + +Order 2. *Spheroelobaceae*. An intermediate layer of the peridium swells +when ripe, forming a star-like structure, which encloses the vegetative portion of the +fruit-body which contains the spores. *Spheroelobus coropuloides* has small, +spherical fruit-bodies which open in the form of a star. + + +A diagram showing the structure of a fruit-body in the family Gasteromycetaceae. +The diagram shows a star-shaped opening at the top, with a central column extending downwards. +Inside the star-shaped opening, there are several smaller spheres connected by branches. +The central column has a series of rings around it, each ring representing a different stage in the development of the fruit-body. +The outermost ring is the largest, and the innermost ring is the smallest. +There are also two smaller circles on either side of the central column, one above and one below. +The diagram is labeled with numbers indicating different stages in the development of the fruit-body. + + +Fig. 128.—*Phallus impudicus* (Stink-horn), somewhat diminished. Fruit-bodies in all +stages of development (5, 6, and 7-9) are seen arising from a root-like mycelium (1); & longish section through the fruit-body (2) showing its cup-like expansion. + +Family 4. *Gasteromycetes* + +The fruit-body is anisocarpic, flaccid at first, and later generally more or less hard and continues closed after the spores are ripe. +The tissue lying immediately inside the peridium is termed the globus; it is porous, containing a larger or smaller number of chambers lined with the hymenium, which is either a continuous + +--- +Note: The text appears to be describing various fungi and their structures, particularly focusing on the family Gasteromycetaceae. It includes descriptions of fruit bodies, peridia, and other anatomical features. The diagrams mentioned in Fig. 128 likely show illustrations of these structures. + +174 + +**SAHIDOMYCETES** + +layer of basidia or else it fills up the entire cavity. The basidia as a rule bear four spores, sometimes eight (Gaster), or two (Hyphomycetes). The tissue of the walls (trama) consists often (Gasteromycetes) of a single layer of cells, which are filled with protoplasm, divided by transverse septa and bearing the basidia; others thicker and thick-walled which do not dissolve like the former on the ripening of the spores, but continue to grow and form a second layer of cells, which may be regarded as highly developed paraphyses. The peridium is either single or double, and presents many variations in its structure and deliquescence. The mycelium is generally a number of string-like strands, living in soils rich in humus. + +Order 1. Tylostemonaceae. Capillitium present. After the rupture of the peritium the fruit-body is formed when the fruit-body is drained on a long stalk. *Tylostemon sessilum*, on heath. + +Order 2. Lycopeideae. Capillitium present. After the rupture of the peritium the fruit-body is formed when the fruit-body is drained on a long stalk. *Tylostemon sessilum*, on heath. + +*Lycopeus radula* has a sterile part at the base of the fruit-body which often forms a thick stalk. The surface of the peritium is generally covered with warts or projections. When young it is green, but becomes brownish when ripe it is dry, and used for stop- +ping the flow of blood. *L. pigmentus*, which grows in woods and meadows, attains a considerable size, its peritium becoming so large as to be almost as high as roundwood. *L. subterraneus* (Fig. +180) is covered with pyramidal warts; in some cases they are very numerous, especially basal part; the external peritium is smooth, and falls away in irregular pieces, leaving behind only a few fragments of the son. *Greater* (Earth-star) has an external peritium composed of several layers, which when the fruit-body opens, gives off a strong smell. These segments are very hygroscopic, and in dry weather bend backwards and so raise the inner peritium into the air. The inner peritium contains the spores + +![Image](image) + +Fig. 180.—Lycopeus radula germination. + +**BASIDIOMYCETES.** +175 + +and capillitia. *G. soliforos* has several apertures in the inner peridium. The other species have only one regular aperture at the apex. *G. arista* has a peridium with two apertures, one on each side of the apex. In this species the external peridium splits into four segments. This last and several other species produce "mycorrhiz" on the roots of Conifera. + + +A diagram showing the structure of a basidiomycete. + + +Fig. 381.—Hymenoporellus olivaceus (fac.) ; II longitudinal section through II toer- (< 4); III section of a section of *H. olivaceus* p & chamber; IV hymenium ; ep., mycorrhiza ; I, conidia ; V, VI, VII sections of *H. olivaceus* ; VIII, IX, X, XI sections of *V.* ; XII basidium with spores belonging to the same Fungus. +Order 3. *Sclerodermataceae*. Cypellitum wanting. The peridium is simple and thick, gleba with round, closed chambers, which are filled with basidia. + +*Scleroderma* has a corky peridium. The fruit-bodies commence their development under ground. *S. olivaceus* (figs. 181 V-TH), has a hard, shiny-black globule, +N + +N + +176 + +**RADIOMYCETES.** + +Order 4. **Nidulariaceae** (Nest-Fungi). Small Fungi of which the fruit-body at first is spherical or cylindrical but upon maturity it becomes cupular or vase-like, and contains several botryoid cells, each of which is a small flask-shaped cell, which are the chambers which contain the hymenium, covered by a thin layer of the gleba, all the remaining portion of the gleba becoming dissolved. On decaying wood. + +**Nidularia** has spherical fruit-bodies containing a large number of botryoid cells, each of which is a flask-shaped cell. *Coryneascus* has fruit-bodies resembling crucibles with discoid peridia, each with a spiny-wrinkled stalk. *Gasterus* is a fungus with a fruit-body consisting of cupules, or cup-like appendages, with scattered peridium, and long-lobed, hence-septate peridial cells. + +Order 5. **Hymenogastraceae.** Fruit-bodies tubercular, globose and subterranean, resembling very closely the Truffles, from which they can only be distinguished with certainty by microscope. The fruit-body consists of a central core, or axis, and the gleba ensholds a system of labyrinthine passages covered with a continuous hymenium. The fruit-bodys persists for some time, and form a fleshly mass, the spores being only set free by the decay of the fruit-body, or when it is eaten by animals. The majority of these fungi belong to the genus *Hymenogaster*, *Metagoniaceae*, *Echinopogon* (Fig. 181 I-V). + +**APPENDIX TO THE BASIDIOMYCETES:** + +**Basidiolichenes** (Lichen-forming Basidiomycetes) + +Several Fungi belonging to the Basidiomycetes have a symbiotic relationship with Algae exactly similar to that enjoyed by certain Ascomycetes, and these are therefore included under the term Lichens (see p. 300). They may be divided into two Orders: + +Order 1. **Hymenolichenes.** To this order belong some gymnocarpic forms: *Corax*, *Ditymonema*, *Ladatina*. + +Order 2. **Gasterolichenes.** To this belong some angiocarpic forms: *Emricella*, *Trichocoma*. + +**APPENDIX TO THE FUNGI** + +1. The Saccharomyces-forms are Fungi which are only known to exist in the form of yeasts, and are therefore higher. + > The last two genera are identical, the hapt part being a Septumite, that of *Corax* a Chroococcete; while the same Fungus—a *Thelephoree*—takes part in a formation of all three (A. Miller, flora, 1903). + + + + + +
Fungi imperfecti (Incompletely known Fungi)
+ +Fungi imperfecti + +Fungi which can multiply to an unlimited extent by budding in nutritive solutions, and in this way maintain their definite size and shape. The bud-buds are usually produced at the ends of the conidiomata. The wall of the conidiomata forms at one or at both ends a small wart-like outgrowth, which gradually becomes larger, and is finally separated from its mother-cell as an independent cell, surrounded by a closed cell-wall (Fig. 103 b, c). + +Fig. 103.—Non-yeast (Aspergillus ceruleus): a b (× 800); c d (× 750) : a cell in the process of forming spores ; a mature sporangium with numerous spores ; b the distribution of the cuticula ; c d germinating spores ; g mycelium-like cell-bodies. + +Under very favourable conditions multiplication occurs - so rapidly that the daughter-cells themselves commence to form buds, before they have separated from their mother-cell, with the result that pearl-like chains of cells are produced. When the yeast-cells have only limited nutrition, with an abundant supply + +178 + +**FUNGI IMPERFECTI** + +of air, at a suitable temperature, an endogenous formation of *spores* takes place. The protoplasm of the cells divides into 1–4 (rarely a greater number) masses (Fig. 182 a, d, e) which surround themselves with a thick cell-wall, and in this state can withstand adverse conditions and periods of dryness lasting for several months. + +The *sporangia* are not ascis since they have no definite form, and a definite wall is lacking between the sporangium and the spores. The spores in the different species and kinds occur varying periods for their development, although exposed to the same temperature, a fact of importance in determining one from another. On germination the wall of the *spore* is destroyed, and each spore gives rise to a new cell, multiplication taking place by budding (Fig. 182 f). The majority of Yeast-Fungi are able to produce alcoholic fermentation in saccharine water. + +The most important of these Fungi is the Beer-yeast (Saccharomyces cerevisiae) with erect, ellipsoidal cells (Fig. 182 b), it is a plant which has been cultivated from time immemorial, on account of its property of producing alcohol by means of saccharine fermenting extracts (wort), derived from germinating barley (malt). Car- bonic acid is also set free during this process. The *Barrel-yeast* (Saccharomyces pastorianus) is used in beer when the brewing takes place at higher temperatures, his cell-chains "sedimentary yeast" (Fig. 182 b), used in the brewing of Bavarian beer, has spherical cells, solitary, or united in pairs. Both these and the other Beer-Fungi include, according to Hansen, several species and kinds. + +The "Ferment of Wine" (Saccharomyces ellipsoides) produces wine in the juice of grapes. Uncultivated yeast-cells are always present on grape-leaves and on the grape-skins, but they do not need any further secretion. A large number of other "uncultivated" yeast-cells appear in breweries mixed with the cultivated ones, and cause different tastes to the beer (S. pastorianus, etc.). S. fæcidius, found, for instance, on the slimy + +Fig. 181.—Saccharomyces regenerans. + +C + +**FUNGI IMPERFECTI** + +discharge from Oake, produces abundant cell-chains on cultiva- +tion. *S. ophiolites* is very frequently met with on all kinds of +sweet fruits, it has one or more species of *Saccharomyces* which have cylin- +drical cells, often united together in chains (Fig. 183); it forms a +whitish-gray mass ("feur de vin") on wine, beer, fruit-juice, etc. +The name "yeast" is applied to this fungus, but it is thought +that this Fungus causes decomposition and oxidises the fluid in +which it is found, but it cannot produce alcoholic fermentation in +saccharine liquids, and it does not form endospores; hence it is +uncertain whether it is true *Saccharomyces*. + +The "Dry-crust" used in baking white bread is "surface- + +Fig. 183.--Oidium fucile. A branched hypha commonly met with by hyphae (rising to +meet each other) forming a chain of cells. The cells are cylindrical, and are connected by +bridges. In the centre of the chain is a large cell, which is the parent cell of the two +cells, the others (intermediate) cells being budding detached from one another; a chain +of cells is thus formed. In the same way, a germinating oidia in different stages (originally much larger than the +other figures)." + +"yeast." In leaven, a kneaded mixture of meal, barn and water, +which is used for the manufacture of black bread, *Saccharomyces* +is employed; this fungus is a species allied to this produces alcoholic +fermentation in dough; with the evolution of carbonic acid, which +causes the dough to "rise." + +2. *Oidium-forma*. Of many Fungi only the Oidium-forma +are known, which multiply in unlimited series without employing +any higher form of reproduction. *Oidium fucile* (Fig. 184) is an +imperfectly developed form which frequently appears on sur- +179 + +180 + +**FUNGI IMPERFECTI** + +milk and cheese. It can produce a feeble alcoholic fermentation in saccharine liquida. Thrush or apthae (O. albicans) appears as white spots in the mouths of children. Several similar *Oidium* fungus are known to cause skin diseases, such as scurvy (*O. schoenleinii*) and ring-worm (*O. tonsurans*). + +b. **Mycorrhiza**. Certain Fungi, which have been found on the roots of many trees and heath-plants, particularly Cupuliferae and Ericaceae, consist of septate hyphae, and belong partly to the Hymenomycetes, partly to the Gasteromycetes. It has been shown that they enter into a symbiotic relationship with the roots of higher plants, producing a condition known as Mycorrhiza. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
180FUNGI IMPERFECTI
milk and cheese.It can produce a feeble alcoholic fermentation in saccharine liquida.
Thrush or apthae (O. albicans) appears as white spots in the mouths of children.
Several similar *Oidium* fungus are known to cause skin diseases, such as scurvy (*O. schoenleinii*) and ring-worm (*O. tonsurans*).
b.Mycorrhiza.
Certain Fungi, which have been found on the roots of many trees and heath-plants, particularly Cupuliferae and Ericaceae, consist of septate hyphae, and belong partly to the Hymenomycetes, partly to the Gasteromycetes.
It has been shown that they enter into a symbiotic relationship with the roots of higher plants, producing a condition known as Mycorrhiza.
+ +DIVISION II. +MUSCINEÆ (MOSSES). + +In this Division a well-marked alternation of generations is to be found. The development of the first or sexual generation (gameto- +phyte), which bears the sexual organs, anthocidia and archegonia, commences with the formation of a prothallus and continues, in the +Liverworts, of a thallus, but in the true Mosses with filaments and +protonema, from which the Moss-plant arises as a lateral bud. +The second or sexual generation (sporophyte), developed from the +filamentous protonema, is a leafy plant with a definite stem. + +The sexuæ generation, the gametophyte. The protonema in the Liverworts is very insignificant, and not always very sharply +demarcated from the more highly developed parts of the nutritive +system. In the true Mosses the protonema is well-developed, and +consists of a branching, algo-like filament of cells, the cell-walls being always plainly obliquely. In the parts exposed to +the light it is green, but colourless or brownish in those parts +which are underground (Fig. 186). The protonema is considered to be a simple plant-body, which develops into a leaf by means of an apical cell; at its apex it may directly develop into a leaf-bearing stem, or these arise from it as lateral branches (Fig. 180 b). + +The more highly differentiated part of the vegetative system, +the "Moss-plant," which is thus developed from the protonema, +is in the "thallid" Liverworts generally a dichotomously- +branched thallus without any trace of leaf-structures (Fig. +184). In the higher Mosses leaves are present. Simple leaves +(amphigastria) are found on the under surface. The higher +Liverworts and the Lesley-Mosses are differentiated into a fila- +mentous, ramified stem with distinct leaves arranged in a definite +massion, resembling the stem and leaves of the higher plants (Figs. +185, 185', 200). + +181 +1 Formerly termed oophyte. + +182 +MUSCINEE. + +True roots are wanting, but are biologically replaced by rhizoids. These are developed on the stems or thallus in the Liverworts they are unicellular, but in the Leafy-Mosses generally multicellular and branched. In the latter group they are considered identical with the protonema, and may become true protonema, and so give rise to the gametophyte generation. + +The internal structure of the sexual generation is very simple. The leaves in nearly all cases are formed of a single-layered plate of cells; in the Leafy-Mosses, however, a midrib is very often formed, and sometimes also, marginal veins; and along these lines the leaves are several layers of cells in thickness. The stem is constructed of cells longitudinally elongated, the external ones of which are narrower and sometimes have thicker walls than the more central ones. Protonema are not found, but in several Mosses they grow in the centre of the absorbing leaf-like structure, longitudinal cells, which represents the vascular bundle in its first + +A lower portion of a Moss-plant with rhizoids (7), one of which bears a reproductive bud (6). The dotted line indicates the surface of the ground; the prostrate prostrate plant (5) is shown at the bottom of the figure. A shows a portion of one of these. B Germinating spores of *Funaria hygrometrica*, with excurrent still unbroken, showing the two polar filaments (3). C A portion of a leaf (4) showing the veins (2) and the margin (1). + +Fig. 385.--A Lower portion of a Moss-plant with rhizoids (7), one of which bears a reproductive bud (6). The dotted line indicates the surface of the ground; the prostrate prostrate plant (5) is shown at the bottom of the figure. A shows a portion of one of these. B Germinating spores of *Funaria hygrometrica*, with excurrent still unbroken, showing the two polar filaments (3). C A portion of a leaf (4) showing the veins (2) and the margin (1). + +MUSCIACEE. +183 + +stage of development. This strand contains elements for convey- +ing water as well as sieve-tubes. Stomata are entirely wanting in +the sexual generation of the Lenfy-Mosses; they are found in a few Liverworts (Marchantia), but their structure is not the same as +in the higher plants. + +The gametophyte sporophore takes place by gemmae or buds which +arise on the protenia, the rhizoida, the thallus, or the shoots, and +become detached from the mother-plant; or else the protonema, +and the older parts of the plant simply die off, and their branches +thus become independent plants. This well-developed vegetative +reproduction explains the great Marchantiae. In some cases, however, +in certain Marchantiaee special cupules, in which gemmae are +developed, are found on the surface of the thallus (Fig. 197 A, s–o). + +A small green plant with a central stem and two leaves extending outward. +Fig. 197.—Marchantia polytricha: a mossy thallus. + +Again, gemmae may also arise from the leaves, and thus the +leaves may act as reproductive bodies. Certain Mosses nearly +always reproduce vegetatively, and in these species the oospheres +are seldom fertilised. + +The first generation bears the sexual organs: both kinds are +fossilised, viz., in one name plant (monococcia), or on separate plants +(dioecia). In the thallid Liverworts they are often situated on +the apex of small stems (gametophores), springing from the surface +of the thallus. In some Lenfy-Liverworts and true Mosses the leaves +which bear the sex organs are arranged in a more or less circular row, +and are arranged more closely than the other leaves to form the so-called +"Moss-flower." The male sexual organs are called antheridia. +They are stalked, spherical, club- or egg-shaped bodies whose +walls are formed of one layer of cells (Fig. 197), enclosing a mass +of minute enclosed cells, each one of which is a mother-cell of + +A small green plant with a central stem and two leaves extending outward. +Fig. 198.—Spermatiacea. + +184 +MUSCINEE. + +a spermatocoid. The spermatocoids are self-mobile; they are slightly twisted, with two cells placed vertically (Fig. 189), while posteriorly they are generally flattened, club-shaped, and often bent at that part the remains of the cytoplasm, the spermatocoid itself being formed from the nucleus. In the presence of water the ripe anthocerous cells, when mature, are ejected; the spermatocoids, being liberated from their mother-cells, swarm about in the water in order to effect fertilisation. + +The female sexual organs are termed archegonia. They are flask-shaped bodies (Fig. 189), the lower, swollen portion (center) having + +A diagram showing the structure of an archegonium. It consists of a long neck (A), a swollen base (B), and a central canal (C). The neck is divided into tiers of four to six cells (D). The central canal contains a row of cells (E). The swollen base contains a single cell (F). + +a wall, in most cases from 1-2 cells thick, enclosing the oosphere (Fig. 189 B, k); the long neck is formed of tiers of 4-6 cells, enclosing a central row of cells—the neck-canal-cells (Fig. 189 A). When the archegonium is fully developed, the walls of the neck-manual-cells become thin and break down, allowing the contents of the archegonium. The meiocyte thus escapes, and, remaining at the mouth of the archegonium, acts in a somewhat similar manner to the stigma and conducting tissue of a carpel, by catching and conducting the spermatocoids to the oosphere (Fig. 189 B, m), with + +MUSCULAR. 185 + +whose cell-nucleus they coalesce. With regard to the formation of the oospheres, it may further be remarked that the lower part of the archegonium originally encloses the so-called "central cell"; but shortly before the archegonium is ripe, this cuts off a small portion, the central-canal-cell, which becomes the egg, and constitutes the neck, and the larger, lower portion be- +comes the oosphere. + +The organs mentioned here, antheridia and archegonia, are present in the Crypto- +genia (Fig. 10), but not in the Gymnosperma sperma. They have always the same fundamental structure with slight modifications of detail. These organs are therefore known as the ARCHEGONIA. + +The fertilization of the Mosseri +has been effected without water. +Rain and dew therefore play a very important part in this pro- +cess, and for this end various modifications of structure are found. + +Figure 10 - Androecium repens. Longitudinal section through a sporangium in the process of division. The upper half of the spores are dividing; p pseudo- +polypodium; s wall of the sporangium; e columella; w wall of the sporan- +gium; v outer layer of cells; n inner layer of cells; f the spermatocyst-cell; +x the spermatozoon with the neck of arche- +gonium [a]. + +Figure 11 - Androecium repens. Transverse section through a ripe sporangium. In the upper half of the sporangium, sur- +rounded by the numerous spores, drawn dia- +grammatically, is seen a large vacuole within +the wall of the sporangium, whose outer layer of +cells is enlaced in four places [b], indicat- +ing the position of the clitellum (see Fig. +10). + +186 +MUSCIACEAE. + +Among the sexual organs are paraphyses—filamentous or club- +shaped bodies—so to be found. + +The asexual generation, the sporophyte (Mosse-fruit or +sporocarpum). As the result of fertilisation the sporophore sur- +rounds itself with a cell-wall, and then commences to divide in +according to the definite laws. The first division is produced by +those dividing cells which produce the wall-cells of the archeo- +gonium (Fig. 190, 199 D, E), and develops into the sporocarpum, +which remains attached to the mother-plant, often nourished by +it, as if the two were one organism. The lower extremity of the +sporophore is usually prolonged into a stalk, which penetrates its +way deep down into the tissue of the mother-plant, but without an +actual union taking place. The central portion of the sporocarpum +becomes a shorter or longer stalk (seta), while the sporophore itself +is reduced to a mere capsule. In this way, as regards the +formation of the spores, the sporophyte very often assumes the +form of a capsule, and deficiences in several ways characteristic of +the various genera (Fig. 192, 193, 194, 195, 200). The basal portion +of the sporophore is called the stoma, and is surrounded by forming +a sheath, the collyris, in which the capsule is developed, but +eventually it ceases to enlarge, and is then ruptured in different +ways, but quite characteristically, in each group. Anatomically, +the stoma is always more or less distinct than that of the true mosses, +but are absent in the sexual generation. + +As the capsule develops, an external layer of cells—the *amphi- +bionites*—forms on its surface. These cells are generally effec- +tiented. As a rule the former becomes the wall of the capsule +while the latter gives rise to the spores. In this Division, as in +the Pteridophyta, the name *archegonium* (Fig. 190 f) is given to +the group of cells inside which germination gives rise to +the male gamete or spore. The archegonium is in general a unicellular layer; in *Sphagnum* and *Andococcus* it is derived from +the most internal layer of the amphibionites, but with these ex- +ceptions it arises from an endogenous cell usually from most +external origin. In the true Mosses and in many other spore- +mother-cells are produced from the archesporium, but in the + +This corpuscle divides by a wall transverse or oblique to the longer axis of the archegonium. From the upper (epiplasmic) cell, the capsule (and seta) is derived, while the lower (hypoplasmic) gives rise to the joint. In Riccia the hypo- +basal half takes part in the formation of the sporocarpum. + +A diagram showing a cross-section of a moss plant's reproductive structure. + +HUCINER. 187 + +majority of the Liverworts some of these cells are sterile and become satellites (cells with sparsely thickened walls, Figs. 190, 191), or are "spore-cells" for the spore-mother-cells, which gradu- +ally absorb the nucleus of the mother-cell and nourish them. +In *Anthoceros*, and almost all the Lefny-Mosses, a certain mass of cells in the centre of the sporangium (derived from the endo- +thecial layer) form a part in the formation of the archesporium, +but forms the so called +"cell of the archesporium" +(Fig. 190, I). +The spores arise in +tetrad, i.e. four in each mother-cell, and are +arranged in the corner of +each tetrahedron, assuming +the form of a sphere or +a trapezium, according to +the mature spore is a +nucleated mass of pro- +toplasm, with starch or +of no other material. +The wall is divided into two layers: the exter- +nal coat (exosporum) +which is greenish, +and in most cases +coloured (brown, yel- +lowish), and the internal +coat (endosporum), +is colourless and not +cuticularized. On ger- +mination the exosporum +is thinned out by the +spore-protrudes, and cell-division commences +and continues with the growth of the protomema (Fig. 185, B-D). + +The morphological explanation which Calkinshev has given of the spor- +gonium, and which is not at all improbable, is that it is homologous with + +Fig. 190.--Anthoceros petro- +phylus. An empty capsule; +the archesporium from off. +(Flag. 25 times.) + + +Fig. 191.--Anthoceros petrophylus. A ripe sporangium: +a) The archesporium; b) the +psperidium; c) the foot; d) the neck; e) the dark- +green exosporum; f) the light-green endosporum +walls are considerably thinned; g) the thin-walled +spore-protrudes; h) the young ex- +tremity of the spore-meri.; j) calyptrae; k) the apex of +the sporangium. (Flag. 25 times.) + + +188 + +MURCINAE. + +an embryo consisting of a very small stem-portion and a terminal spore-producing leaf. This will be further explained in the introduction to the Flowering-plants. + +In the Liverwort the young sporogonium lives like a parasite, being nourished by the sexual generation (only in Anthoceros has it a slight power of assimilation). In the Leafy-Mosses, on the other hand, the vegetative generation is found from abundant assimilation (Fernaria, Pogonocrium) to almost complete "parasitism" (Sphagnum, Andromeda). In the majority of the opereolate Mosses the sporogonium has a more or less large stem-portion, which is able to form a large portion of the material necessary for the development of the spores, so that it chiefly receives from the sexual generation the inorganic substances which must be obtained from the soil. The more highly developed and assimilative systems of the sporogonium, as may be seen, are presented here. + +Anoplectum. In some opereolate Mosses it has been possible to obtain a protonema with small Mean-plants from the sea, when severed from its Moss-plant, and placed in water. + +The Mosses are the lowest plants which are provided with stem and leaf. They are assigned a lower place when compared with the higher Cryptogons, partly because there are still found within them the Dicots, but also because they generally have no typical roots awaiting and the anatomical structure is so extremely simple, and partly also because of the relation between the two generations. The highest Mosses terminate the Division, the Mucronae. The Stereophyta having had a common origin in the Algae-like Thallophyta. + +They are divided into two classes: + +Herpatice, or Liverworts. + +**Class** **LIVERWORTS** (Liverworts). + +The prostrate part is slightly developed. The remaining part of the vegetative body is either a prostrate, often dichotomously-branched thallus, pressed to the substratum (thalloid Liverworts), with or without scales on the under side (Fig. 104, 197); or a thin, flat leaf-like blade (leptodermoid Liverworts), with leaves, which are borne in two or three rows (Figs. 105, 198), viz., two on the upper and, in most cases, one on the under side. The leaves situated on the ventral side (amphigastria) are differently shaped from the others (Fig. 106 a), and are sometimes entirely absent. + +MUCIGEN. 186 + +In contradistinction to the Leafy-Mosses, stress must be laid on the outspread and anisocarpic of the vegetative cells, i.e., the very distinct contrast between the leaves exposed to the light and the ventral side turned to the ground. Veins are never found in the leaves. + +The central part of the archegonium (antheridium) continues to grow for some time, and encloses the growing embryo, but when the spores are ripe it is finally ruptured by the sporangium, and remains situated like a sheath (capsula) around its base. The sporangium opens longitudinally, by valves or teeth (Fig. 194, 195, 197 b), very similar to those of the antheridium. The capsula is somewhat (except in Anthoceros, Fig. 194); but on the other hand, a few of the cells lying between the spores are developed into + +A diagram showing a plant with two spores. +Fig. 194.—Anthoceros lepidus +(see text). A-E. Magnification. + +Fig. 195.—Plagiostele splendens: a. margin, and b. an open capsule; p. involucrum. The vertical line in each leaf is lighter than the dorsal edge, and occurs near by the dorsal edges of the mesophyll. + +clateri (Fig. 196). e. spirally-shaped cells with spirally-twisted thickening, which are hygroscopic, and thus serve to distribute the spore-water. These are seen in Fig. 189 C, not yet fully developed, as long cells radiating from the base of the sporangium. They are wanting in Eriocaulon. + +Round the entire archegonium, (or group of archegonia, when several are developed on the same receptacle) a sheath—the funiculare—is often formed, which projects beyond the archegonium, and is sometimes connected with the sheath of the archegonium (Fig. 195 p). In the Marchantiaceae each archegonium is enclosed in a loose investment, the perigynium, which is developed as an outgrowth from the cells of the axis. + +An illustration showing a plant with two spores. +Fig. 196.—An +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 b.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 c.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 d.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 e.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 f.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 g.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 h.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 i.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 j.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 k.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 l.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 m.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 n.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 o.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 p.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 q.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 r.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 s.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 t.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 u.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 v.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 w.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 x.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 y.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 197 z.—A +clateri with two +spores. + +A diagram showing a plant with two spores. +Fig. 200.—A clateri. +200 + +This page contains illustrations of plants and diagrams related to their anatomy and structure, particularly focusing on the archegonia and sporangia of various species within the Marchantiaceae family, including Anthoceros and Plagiostele splendens. The text describes how these structures develop over time, from being enclosed by an outer sheath to eventually opening up longitudinally to release their contents upon maturation of the spore-producing cells within them. It also mentions that in some species such as Eriocaulon, these structures may be lacking entirely, while in others they form an investment around individual archegonia or groups thereof called "funiculare." + +190 +**MUSCIACEAE.** + +The majority of the Liverworts are found in damp and shady places, pressed to the substratum; a few are found floating in fresh water. + +**Family 1. *Marchantiae*.** + +This embraces only forms with a thallus, which is more or less distinctly dichotomously branched, in some, one or two rows of this branching being visible. On the upper surface of the thallus are found large air-chambers. + +Order 1. *Ricciaceae*. The sporangia are, with the exception of a few genera, situated simply on the surface of the thallus, and consist only of a capitate without foot or stalk. They always remain enclosed by the wall of the archegonium (only thus), and open only by its dissolution. Elaters are not developed. Some genera are found in water like Duckweed—*Equisetum glaucum* growing on damp clay soil. *R. flotans* and *R. natans* float in stagnant waters. + +Order 2. *Coriaceae*. (Not native). Intermediate forms between the preceding and the following order. In internal and external structure mainly resembling the Marchantiaea. *Coriopsis*—*Brachia*. + +Order 3. *Marchantiaceae*, are large, fleshy forms. The + +Fig. 197.—Marchantia polyphylla. A Female plant (fast erect); a + b are archegonia; c is a young sporophyte; d is a mature sporophyte; e is a young plant (fast erect). B An archegoniphore seen from below, the short-stalked sporangia are seen placed in both directions on the surface of the thallus; f is a mature sporophyte; g is an archegoniphore half turned to show the archegonia (b); h is the aperture of the plant in which they are enclosed; i is a mature sporophyte; j is an archegoniphore seen from above. + +6 + +MUCINEE. 101 + +surface of the thallus is divided into small rhombic areas, in the centre of each of which is found a large, peculiarly constructed stoma (Fig. 197 A); beneath each of these a large air-cavity is to be found, through which the gas passes to the surface, where alga-like cells project into it; these contain chlorophyll and are therefore the assimilating cells. The antheridia and archegonia are each found aggregated on specially formed branches (some-what resembling the 'horns') projecting from the surface of the thallus. The antheridia are situated on the upper side (Fig. 197 C, D) and the archegonia on the lower (Fig. 197 A, B), near the centrally-placed stalk. + +Marchantia polymorpha has two directions (Fig. 197), and very common on damp places in Lombarria (South Europe), frequently found on flower-pots in conservatories; *Pretiosa*, *Fogolatta*, *Rebella*, *Targioni*. + +Family 2. Anthocerotaceae. + +These have an entirely different structure from that of the globular-shaped Italian. In its intermediate position between Nothoceros and other forms, which have crossed their way through the stomata situated on the under side. The anthoceridia and archegonia are arranged in a single row inside the thallus. The capsule resembles a long thin pod; it has two valves and a columella. *Anthoceridia* (cf. *Lentia*, Fig. 194, and *pannucia*). + +Family 3. Jungenmanniaceae. + +Some forms in this family have a thallus in which leaf-like structures are developed, while in others (*e.g.* *Metzgeria*, *Palaeo*) they are entirely absent. The majority, how- ever, have round, thick stems bearing dorsally two rows of leaves and one row ventrally; but those of these have leaves "underlying" (Fig. 195), while in others (Fig. 195) they are "overlying." (See Figs. 185, 188, with explanatory notes.) + +The plants are spherical, stalked, and situated singly on the axis of the branches, and open by four valves (in *Sphaerocarpos* they are indistinguishable). + +All the forms in this family were formerly reckoned as belonging to one genus, *Jungenmannia*, but now they are divided into several, arranged as follows— + +W.R. + +Fig. 196.—Frontal dis- section. Portion of a branch showing the leaves below and a bud above the anterior end of a valve; at the same dorsal line a ventral leaves is "overlying," i.e., at the anterior edge of this valve is a small portion of the edge of the preceding one. + +192 + +**MUSCINEE.** + +I. *Anacrostis*. The archegonia are situated on the upper side of the thallus or stem, placed laterally, and covered by an "involucre," formed by the calyptra together with the tissue of the stem or thallus. + +a. *Aneatellus*. Without any clavate: *Sphorocarpus*, *Ricola*. +b. *Nica*. *Thalidum*. *Anemone* genipos, in damp situations; +*Metzgeria furcata*, on trees; *Pellia epiphytica*, in damp situations; +*Blasia pusilla*, on damp clay soil, in the shade (scales are present on the thallus). +b. *Vallis* and *dorstentorval*: *Hepaticae* hooder. + +II. *Acroctis*. The apex of the stem or of certain branches is adapted for the formation of female shoots. The archegonia are most frequently aggregated on the apex of the shoots, and are conical, or cup-shaped, or both. Between them and the archegonia, enclosing the latter, a peculiar cup-shaped organ (the involucre) is formed. This group only includes leaf-bearing genera: *Fritillaria*, *Zibadia*, *Meditablen*, *Phytolacca*, *Calyptogena*, *Lupinella*, *Montegeyranum*, *Lepidocolea*, *Jungmannia*, *Scopularia*, *Plagiochila*. + +**Class 2. Musci frondosi or veri (True Mosses).** + +In this class the prothallus is well developed, and resembles a branched filamentous Alga, from which it can be easily distinguished by its oblique scapes (in Syngamia it is a cellular expansion). The Moss-plant, which is developed directly from the prothallus, is a simple shoot, usually cylindrical, but slightly constructed on all sides. The leaves are arranged spirally, the most frequent divergence being $9 \div 4$ (Fig. 200 A). A midrib is often present and also marginal veins formed by longitudinally elongated cells. In some cases vein-layers form one layer in thickness. In *Leyonochlaena* the leaves are generally composed of more than one layer. + +The stem grows by means of a three-sided, pyramidal, apical cell which produces two rows of segments, each segment forming a leaf. The lateral branches arise from the lower portions of the segments, the upper portion of which does not take part in the construction of the leaf. From their mode of origin the branches are not axillary, and differ in this respect from the Flowering-plant. + +The ventral portion of the archegonium is very early ruptured. + +**MUCINEAE.** + +at its base by the growing sporangium, upon which it remains, and it is thus raised into the air, forming a "hood," the calyptra (Figs. 192 ; 200 B). In the Sphagnaceae the hood is not present; in this order, as in the Laverwort, the archegonia remain at the base of the stem, and are surrounded by a thick, somewhat dehiscent; the upper portion (pericarpium) being separated along a specially constructed ring of cells, and falls off like a "lid" (Fig. 200). Only in a few forms (Families 2 and 3) does any variation in this respect occur. In all other cases, however, the exception of *Archidium*), there is always present in the sporangium a central mass of cells, the *collema*, which take no part in the formation of the spores. The collemata, in some, does not reach quite to the summit of the stalk, but is only found on one side of it; in others it is more extensive, and extends over the whole of the stalk and covers the collemata (Aubretia, Fig. 190 ; *Sphagnum*, Fig. 190 D); but in the majority of Mosses the collemata extends to the lid, so that the space containing the spores becomes a hollow. + +The sporangium is generally raised on a long stalk; in the great majority this stalk is formed from the lower half of the oospore and belongs to the sexual generation—it is thus known as the **sakula**. In some species (e.g., *Sphagnum*) very rarely do the sporangia are raised upon a long stalk (*pedunculus*) developed from the summit of the sexual generation (Figs. 190, 192). In the latter figure an archegonium (a) is seen attached to the pedunculus (b), and is shown in various stages during the course of its development. The summit of the pedunculus is enlarged to embrace the foot of the sporogonium (Figs. 192, 190 D). + +A. The sporangium is supported on a pedunculus ; the collemata does not extend to the operculum. + +Family I. *Sphagnaceae* (Bog-Mosses). + +The protonema has been already described. The stem is regularly branched owing to the fact that a branch, or collection of branches, grows out from each node. The leaves are closely covered with leaves, some are erect, while others hang down and surround the stem. No rhizoids are developed. These Mosses are of a whitish-green colour, and when water is present are always saturated with water; they are therefore called *hydrophytes*. In the construction of the stem and leaves. The stems are covered by an external layer of large clear cells, without chlorophyll, but with annular or spiral thickenings on the walls, which are also + +194 +HUSCINAE. + +perforated by large holes. By means of capillary attraction, water is thus raised to the summit of the stem. Similarly constructed cells are also found in the leaves, but they are surrounded by a net of very narrow, chlorophyll-containing cells (Fig. 199 F), whose colour is thus to a great extent lost amongst those which are + +A plant with long, thin branches and terminal arachnids. The upper stem-bearer has three arachnids on its branch, while the lower stem-bearer has two arachnids. A Group of three arachnids: the central one (a) is formed from the apical bud, the other two (b and c) from lateral buds. D Portion of a leaf with a single arachnid (v); e calyptera; or neck of the arachnidium; p pseudopodium. E ripe arachnidium with greenish-yellow body and brownish-black head; f portion of a leaf still enveloped by the peristomium; g to h a hair-like branch. F Portion of a leaf, formed from a stem-bearer's peristomium; i chlorophyll-containing cell; j apical thickening. + +Fig. 199.—Sphagnum arcticum.—A The upper portion of a plant: e branches with arachnids; ah branches with terminal arachnids and peristomium; b the upper stem-bearer with two arachnids; c the lower stem-bearer with two arachnids. C Group of three arachnids: the central one (a) is formed from the apical bud, the other two (b and c) from lateral buds. D Portion of a leaf with a single arachnid (v); e calyptera; or neck of the arachnidium; p pseudopodium. E ripe arachnidium with greenish-yellow body and brownish-black head; f portion of a leaf still enveloped by the peristomium; g to h a hair-like branch. F Portion of a leaf, formed from a stem-bearer's peristomium; i chlorophyll-containing cell; j apical thickening. + +colourless. This anatomical structure is an essential condition for the formation of peat. The Bog-Mosses grow by preference on + +**MUSCI.** 195 + +moors, which they cover with a thick carpet saturated with water. +The lower extremities of the plants perish very rapidly, and gradually become converted into peat, and the branches thus separated from the stem, form the common peat-beds of plants. The sporangium (Fig. 199 D) are spherical, but with a short stalk. They open by a lid, but have no annulus. The archegonium (Fig. 190 C) persists at the base of the sporangium as in the Liverworts. Only one genus, Schizogonium. + +Family 2. Schizogonaceae. + +The Moors which cover the moors are of a brownish-black colour and are found living on rocks. The sporangium resembles that of the Liverworts inasmuch as it opens by four valves, but these continue attached to each other at the apex of the sporangium (Fig. 193).—There is only one genus: *Andreae*. + +B. The stalk is formed from the lower portion of the sporangium. This columella is continued to the summit of the sporangium and united with it (*Archidium* has no columella). + +Family 3. Cleistocarpaceae. + +The fruit does not disperse in the regular way, but the spores are liberated by decay. They are enclosed in a case, which remains with their protoplasm until the sporangium is mature. The archegonium remains sessile at the base of the short cap-like stalk, and is not raised into the air (compare Hapalites)—*Pleurozium*, *Zygodon*. + +Family 4. Stigmacarpaceae. + +To this belong the majority of the Moors, about 3,000 species. +The capsule open as in Sphagnum by means of a lid (*cercula*)—which is often prolonged into a beak. Bound the mouth of the opened capsule, a number of peculiar yellow or red teeth are to be found. These teeth are either four or five in number, or four or a multiple of four (8, 12, 32 or 64). The formation and constancy of these teeth are widely different, and on this account are used by Systematists for the purposes of classification. In some Mosses (Fig. 200 G, D) there is a double row of teeth. Except in *Trematodon*, all these forms consist of cells, but in *Sphagnum* strongly thickened portions of the wall of certain layers of cells belonging to the lid, and persist when this falls off. They are strongly hygroscopic; their annulus consists simply of a sheet of the lid, in which they lie; they are therefore aided in drying by these cells with thickened walls, situated at the wall of the lid near the base of the tooth. This ring is known as the columella. The archegonium is raised into the air like a hood, the calyptra, which + +196 + +either covers the sporangium on all sides (having the shape of a ball), or is split on one side (Fig. 200, B, h). + +Among peculiar forms may be mentioned : *Sphaecium*, which is especially remarkable for the collar-like expansion at the base of the capsule. *Fusidium* has a similar structure, but the leaves are arranged in two rows. The leaves are boat-shaped and half embrace the stem. + +*Ceratocystis*. The leaves are circular. The barren cones resemble Fern-leaves; they have two rows of leaves, which are alternately disposed, and alternate with the fertile ones. The fertile cones have an ordinary appearance. + +*Coryne*. The leaves are compound of four teeth, which are formed from entire cells. *T. perfoliata* has peculiar gemmae. + +The family is divided into two groups, according to their habits. In the growth of whose main axis is limited and terminated by the formation of the sexual organs; and in the second group, whose sporogonia are situated on special lateral shoots, while the growth of the main axis is unlimited. + +Order 1. *Acarocarpi*. Family of plants with a single leaf, showing the peristome 19, b. The leaves are simple, entire, and without petiole. + +Duncanius (D. serrupinum, common in forests). *Dicranum*, *Cymbodium*. + +Order 2. *Leucobryaceae*. Peridium with 16 teeth. Leaves with three or more layers of cells, of which the external ones are arc-convexing and perforated (as in the Sphagnum), the middle one containing chlorophyll. *Leucobryum*. + +Order 3. *Pseudostenaceae*. Peridium as in the preceding ones. The leaves are simple, entire, and without petiole; the midrib of the leaf bears wing-shaped outgrowths. *Cronartium*, *Fusidium*. + +Order 4. *Seligeraceae*. Peridium with 16 undivided teeth. Very small. Hook-shaped leaves. + +Order 5. *Potatiaceae*. Peridium with 16 teeth, which are divided almost to the base, or with 21 teeth. Calyces hood-like.--*Zurkia* (Z. morsula, Z. megalos). *Podostoma*. *Lepistemon*.--*Graziola purpurea*.--*Ditrichum*.--*Potria*. + +A diagram showing the structure of a plant. +**Fig. 200.** --A Hygromia pleurosp., B and C Sporangiun, with both (b) and sporangia (c) shown in section (d). D The peristome of *Coryne*. E The peristome of *Tetracystis*. + +**MUSCINEAE.** 197 + +Order 6. **Gramminaceae.** The leaf-cells are often papillose; in the upper portion of the leaf, small, and of roundish shape. The calyptus is most frequently found on the lower surface of the leaf, but in some cases a short-stalked capsule, is found on trees. --*Cocconodon.*--*Hedwigia.*--*Grimmia.*--*Gymno- +trichum.--*Chasmanthium.* + +Order 7. *Schizostegaceae.* The stems are of two kinds (see above); *Schizostegum amandaceum,* in leaves, has a bright emerald pronotum. + +Order 8. *Orchidaceae.* The flowers are large, elliptic or lanceolate, with large, ellipsoid nut (see above). *Spatholobus* (occasionally on mosses). + +Order 9. *Funiculaceae.* *Cephalon* pecten-shaped. *Funiculus (F. hagoromus)* has a very long, narrow, and slightly curved stem, which is covered with white, and strengthening with moisture; *Physocephalum.*--*Dioscorea.* + +Order 10. *Bryaceae.* The capsules is thicker towards the apex; most frequently found on mosses. --*Anomodon.*--*Podocarpus.*--*Pseudospor- +dium.*--*Mucuna.*--*Hymenium.*--*Arbuscina.*--*Wurbsa.*--*Lepidoptera.* + +Order 11. *Polytrichaceae.* Single perithecium, formed by 5, 8i, or 64 teeth. +Leaves: *Polytrichum* long and narrow; *Polytrichum* long hairy calyptus. +*Cyanotaenia* (c. amandaceum, in forests). + +Order 12. *Geogarceae.* Perithecium with a tent (see above). *Zetaleia* +(*T. johannis*) is a very common plant. + +Order 13. *Burmannaceae.* Capsule asymmetrical; double perithecium: the interior one conical, with 10 or 22 longitudinal folds.--*Burmannia* (*E. opulenta*)--*Ophiogeton.* + +Order 14. *Pluurocarpi.* + +Order 15. *Fominatiales.* Long, floating Water-Mosses. *Fominatia* (*F. +antipartite*) is found in streams). *Dichogloea.* + +Order 16. *Huckelkernaceae.* +*Huckelkernum:* Fertile branches, with papillose or warty leaves.--*Thuidium.*--*Thuja-like* + +Order 17. *Pterogoniaceae.* +*Pterogonium filiforme*, etc. + +Order 18. *Fabronaceae.* +*Acanthostoma.* + +Order 19. *Lemnaceae.* Floating plants with flat, leafy branches. +The leaves are smooth, new, without longitudinal folds.--*Waterweed.* + +Order 90. *Hypnaeaceae.* The leaves are smooth with squares, often ladder- +like; 300-400 species of this family are known to us: --*Hypnum.* +*Bryophyllum.* +*Cystopteris.* +*Lycopodium.* +*Pleurocarpium.* +*Euryale.* +*Himantia.* +*Orchideum.* +*Rhodinum.* +*Lentenwort.* +*Lemna.* + +The leaves of these plants grow in great numbers, and growing thickly massed together, they form an important feature in landscapes (for example in the Alps and in the Pyrenees). In the Northern and Arctic regions the Mosses are very plentiful, and in many parts of the vegetation, while in the Troops they are insignificant. + +Species of Hypnum and Pterigonia, like Spongiae, play an important part in the formation of peat. + +DIVISION III. +PTERIDOPHYTA (VASCULAR CRYPTOGAMS). + +The alternation of generations is as distinct in this Division as in the Mosses, but the sexual generation consists of only a small thallus, the prothallium, which bears directly the sexual organs, antheridia and oogonia. The gametophytic generation, which arises from the germination of the oospore, is generally a simple short-lived sporangium, but a highly developed, generally perennial plant provided with stem, leaves and true roots (Ferns, Horsetails, etc.), the latter being composed of leafy stems. In this latter case, however, the tissues are differentiated into epidermis, ground tissue and vascular tissue; in the last named the bundles are closed, and in the majority of cases concentric. + +The sexual generation, gametophyte, or prothallium, is always a simple sporangium bearing antheridia and leaf-like (Figs. 205, 215, 221, 229, 235, etc.) It is very small, even in cases where it attains the greatest development, and consists only of parenchymatous cells. The prothallium is nourished by hair-like roots (chlorophyllous) that grow directly from the base of the leaves for fertilisation of its oospore. + +The ANTHOCYTHEA exhibit great variations in structure which, however, must be considered as modifications of the fundamental types found in the Mosses. These modifications will be mentioned under the various families. The spermatocysts are always spirally coiled, self-motile, protoplasmic bodies, with most frequently a large number of fine cilia on the anterior end (Figs. 206, 207). The spermatozoa are produced from the front part of the mother-cell, and portions of the cytoplasm often remain for a time attached to their posterior end. + +The sporangia are distributed throughout the entire Division, and more closely resemble those of the Mosses. They are, as in the previous Division, principally flask-shaped; but the + +188 + +PTERIDOPHYTES. +199 + +central portion, which encloses the oosphere, is always embedded in the tissue of the prothallium, so that the neck, which is formed of 4 rows of cells, projects above the surface (Figs. 201 b, 222 b). The archegonium is shown in the accompanying figure (Fig. 201). The archegonium is developed from a surface cell, which divides into three cells by two walls in a direction parallel to the surface of the prothallium (Fig. 201). The intermediate one (a) divides perpendicularly to the surface of the prothallium into four cells, which again divide parallel to the surface and form the neck (b), 2 and 3). The intermediate cell projects upwards into the neck and divides into two, + +Fig. 201.--Pteris serrulata. Development of archegonium. + +the lower one, after the separation of the ventral canal-cell, becoming the oosphere, and the upper one the neck-canal-cell (c, in 2 and 3). + +As in the Mosses, the divisional walls of the neck-canal-cells become detached from each other during the development of the archegonium. Fertilisation takes place as in the Mosses, and the passage of the spermatoids, along the neck, to the oosphere, has been observed. Water (rain or dew) is similarly necessary for the formation of the archegonium in this case also. + +The other classes of the Division chiefly deviate from the Ferns in having the archegonium sunk deeper into the prothallium, and the neck reduced in length (compare Fig. 201 with Figs. 216, 222, 255, 256). + +199 + +200 +FREIDOFHYTA. + +According to the nature of the spores, the three classes of the Vascular Cryptogams are each divided into isoporous and heteroporous groups. + +I. The **isoporous** Vascular Cryptogams have only one kind of prothallium, but all developed from this is in some cases monocious, bearing both antheridia and archegonia; but in others there is a distinct tendency for each prothallium to bear only antheridia or archegonia (directions)—true Ferns and Lycopodium. + +In Equisetum, the prothallium is large, and bears two kinds of prothallia, one of which bears only antheridia (male), the other only archegonia (female); but the one that bears antheridia may be transformed into the one that bears archegonia. + +II. In the higher group, **heteroporous** Vascular Cryptogams (Saginatella and Ioites, etc.), there are two distinct kinds of spores, the small, microspores, and the large, macropores. The microspores produce and produce prothallia which bear only antheridia. The male prothallia are female, and produce prothallia which bear only archegonia. + +Corresponding to this difference in spores there is also found a difference in the prothallium. In the prothallium of the Isosporae the prothallium is large, and either green, leaf-like, and provided with rhizoids (most of the Faraus, Horsetails, etc.), or subterranean, pale-coloured, and globular (Ophioglossum, Lycopodium). It lives vegetatively for a fairly long time, and generally produces only one kind of prothallium—either male or female. The prothallium in the Heterosporae is gradually more and more reduced, its independent and vegetative life becomes less and less important; it becomes more dependent on the mother-plant, and finally disappears entirely; not at all. The antheridia and archegonia become reduced in number to one, and also degenerate in point of development. + +It may here be remarked that the gradual development of the antheridia and archegonia is due to two kinds of spores, and the progressive reduction of the prothallium and sexual organs which is found in this Division, is continued to the Gymnosperms and Angiosperms. The microspores are in these called pollen-grains; they contain a protoplasmic mass surrounded by a wall. The macropores are termed embryo-aecia; and the female prothalium, the endosperm. + +The asexual generation, sporophyte. When the oosphere, + +A diagram showing different types of spores and their corresponding prothalli. + +PEERIDOPHYTA. +201 + +which in this case as in all others is a primordial cell, is for- +tified, it surrounds itself with a cell-wall and commences to divide into a number of cells, to form the embryo. + +The first dividing wall (basal) is nearly horizontal and in its direction the hypocotyl grows. The second dividing wall is vertical, and the next perpendicular to the other two. The coeophore, therefore, is now divided into eight octants by these three walls. The basal wall divides the embryo into a high and a low part. In the former the first root develops, in the latter the stem and leaves. After the for- +mation of the octants the development proceeds in somewhat different ways in the various parts of the embryo. The first root grows upwards, developed from the hypocotyl half which remains enclosed in the prothallium, and consequently separated from the prothallium by the young plant until it is able to maintain itself (Fig. 203). The position of the first root in the coeophore depends on the position of the coeophore in the archegonium and prothallium, and is independent of gravity. + +A diagram showing the development of a seedling in a peeridophyte. +Fig. 203.—Aetinaea capitula senescens. Vertical section through a prothallium (f.f.), with a young plant inserted on its under side (top, about 1/3 times), of the first root, and a leaf (bottom, about 1/3 times), of the second root. The upper part shows the upper +aspect of the stem; A the rhizoids of the prothallium; n unfertilized antherozoid. + +In the Mosses the asexual generation is the sporangium, which is limited in its development and to a great measure dependent upon that of the gametangia. As in this case so is it also in the +Peeridophyta this generation is an independent and highly developed plant, provided with stem, leaf, and true roots, and has in many instances an unlimited development. The Peeridophyta are the lowest Division of Bryophyta. The root of this plant is very similar in nature to the primary root of the Monocotyledons; it very soon dies and is replaced by others which are more per- +manent, and developed upon the stem (adventitious roots); roots are very rare. The leaves are simple, without veins or midrib. The differentiation is, however, not so complete as in the Flowering-plants, and so many leaf-forms are not found. The various members of these plants are anatomically much higher than in the + +202 +PERIDORIFRIZA. + +Mosses, having an epidermis, a ground tissue with variously differentiated cells, and a highly developed vascular system. The vascular bundles, like those in the Monocotyledons, are without cambium, and closed; they therefore incapable of any increase in thickness. The leaves are also but little increased in bulk with the best round the wood (Fig. 203). The wood is almost entirely made up of scalariform tracheids. + +In *Ferns* a secondary thickening takes place by a cambium, which is formed inside the epidermis. This cambium gives rise to the exarch and endarch wood towards the interior. --Erythrophyllum has also a thickening growth. Collateral vascular bundles occur in *Gomandra*, *Equisetum*, and the leaves of many *Polypodiaceae*, etc. + +It is a point of special interest, that the gigantic forms of *Ferns*, *Equisetums*, and *Club-Mosses* (which flourished in earlier geological periods), have attained their highest development possessed some means of increasing in thickness. + +The sporangia are in all cases cupule-like, and burst open when ripe to eject the spores. They are now always situated on the leaves (in *Lycopodium* diacne, in the axils of the leaves, or above these, on the leaf-stalks, or on the stem). In some forms (*Leptopteris* angustifolia), the sporangia are derived from a single epidermal cell; in others (*Equisetum* angustifolium), from a group of epidermal cells, which lie beneath the epidermis. In the first group a primitive mother-cell (archesporium) is formed, which divides commonly into sixteen special mother-cells. In the latter group, on the other hand, a number of epidermal cells divide into two each; from each sporangium three different tissues are generally developed; an innermost sporogenous one (e.g. fig. 204 A), which arises from the archesporium; an outermost one, which forms the wall (a), + +Fig. 203.--Portion of the stem of a Fern. Above to see richly developed secondary thickening. Below to see different forms and size. The strobilus figures on the right side; the stem are here half-length. + +are derived from a single epidermal cell; in others (*Equisetum* angustifolium), from a group of epidermal cells, which lie beneath the epidermis. In the first group a primitive mother-cell (archesporium) is formed, which divides commonly into sixteen special mother-cells. In the latter group, on the other hand, a number of epidermal cells divide into two each; from each sporangium three different tissues are generally developed; an innermost sporogenous one (e.g. fig. 204 A), which arises from the archesporium; an outermost one, which forms the wall (a), + +PTERIDOPHYTA. +203 + +and may be one or, more rarely, several layers in thickness; and an intermediate one, the tapetum (Fig. 204 A, B, C), which is rich in protoplasm, and whose cells are dissolved so that the spores float freely in the liquid provided. The spores arise as in the Mosses (in tetrad), by the successive division of the initial mother-cells, and according to the manner in which they are arranged in the mother-cell have either a tetrahedral form, with a large base resembling a segment of a ball, or are oblong (bilateral spores). Their construction is the same as in the Mosses (p. 187). + +The spore-formation in its earliest commencement takes place in the same way in the Disporous and the Heterosporous Vascular + + +A diagram showing the formation of spores in a plant. It shows two stages: A, where the spores are formed within a tetrahedral division of the mother cell; and B, where the spores are released into the surrounding medium. + + +Fig. 204.—Sphagnum squamulatum. A young sporophyte, which may develope either microsporangia or macrosporangia. B Cryptogramma; but from a certain point, after the tetrahedral divi- +sion, a difference occurs with regard to the macrosporangia. All +the spores formed in the microsporangium may complete their +development; but those which are formed in the macrosporangium +are generally aborted. In some cases, however, these latter +consequently attain a much larger size (see Fig. 250.—The series to +the left are microsporangia; those to the right, macrosporangia). +Apogamie. In some Ferns (Pteris cretica; Asplenium filix-mas, var. cristatum; +A. filix-mas, var. virens) there is no sexual reproduction at all; fertilization +being effected by means of a bud from the prothallium. This is known as apogamy, +or loss of the power of sexual reproduction. The antheridia are generally +more or less developed; archegonia are entirely wanting in Asplenium mas, var. + +204 + +204 +PTEIDOPHYLLA. + +crinifolia. This variety has probably only become apogamous through culti- +vation. +Many specimens of *Eutrema incurvatum*, in a lake in the Vosges mountains, +produce in the place where the sporangia are usually found, a vegetative shoot +which is sterile, but which produces a fertile shoot at its base. This is not so in this case. Some specimens have sporangia on some leaves, and shoots on others. + +Anemophyllum, or the formation of prothallus instead of sporangia and spores on the leaves, is found in *Atriplex hortensis*, var. *clerodorum*. In this case the florets are sterile, and the prothallus is only to a certain extent, and from these arrested sporangia the prothallus is produced. The leaves are entirely wanting in this variety, and in *Deplidium caeruleum*, var. *pallidum*, sporangia are completely wanting. Compare the Monera (page 186). + +The Vascular Cryptogams are divided into three large classes, in each of which a progressive development can be traced from the sporophyte to the heterosporeous forms, but some of these are now +only known as fossils. + +Class 1. Filicinae (Ferns).—The stem is small in comparison with the leaves, and branches are only seldom, and then by lateral shoots. The leaves are scattered, large, often deeply divided, and of various highly developed types. The under surface of the leaves are rolled up in the bud, having what is termed circinate venation. +The sporangia are situated on the edge or on the lower side of the leaf, and are either sessile or stalked. They are borne (sporophylls) being often the ordinary foliar-leaves; but in few cases do they appear to be fertile differ from the barren ones (a higher stage in development). +The fertile leaves are not confined to definite parts of the shoot, and do not limit its growth. The archesporium is most frequently single. + +A. Isosporous: Sub-Class 1. Filices (True Ferns). +B. Heterosporous: Sub-Clas 2. Hydropteridaceae (Water +Ferns). + +Class 2. Equisetinae (Horsetails), in its widest meaning.— +The leaves in this class are small in comparison with the stem. +They are arranged in whorls, and unite to form a sheath. The +sporangia are situated on specially modified, shield-like leaves, +which are attached to the sheath by a stalk. This sheath is cone +borne terminally, and limits the growth of the shoot. The +sporangia are developed from a large group of epidermal cells, the archesporium being single. +A. Isosporous: Sub-Class 1. Equisetaceae. Existing forms. +B. Heterosporous: Sub-Class 2. Extinct forms. + +FIERIDOPHYTA. +205 + +Class 3. **Lycopodiine** (Club-Mosses). — Roots generally branching dichotomously. The leaves are scattered or opposite, and in proportion to the stem very small, undivided, and simple. They are scale-like and triangular, tapering from a broad base to a point, and usually with a midrib. The sporangia are numerous, and almost in every case on the upper side of the leaf or in the axil of a leaf; but in some cases they are borne on the stem, just above the leaf-axil. The sporangia arise from groups of epidermal cells, which are often elongated, and differ from the foliage-leaves; they are then arranged in cones placed terminally on branches, thus limiting their growth. + +A. *Isosporous*—Sub-Class 1. Lycopodium. +B. *Heterosporous*—Sub-Class 2. Selaginella. + +Class 4. **Filicine** (Ferns). +The characteristics of this class have already been given on page 204. + +The class is divided into two sub-classes.— +1. *Tea Tree Fern*, *Filices*, have one kind of spore which generally develops monocious prothallus, relatively large and green; the other kind of spore develops dioecious prothallus (sex), which are often covered but not enclosed by an indusium. +2. *Water Fern*, *Hygropteridaceae*, have microsporangia with many (4-16) microspores, and macrosporangia, each with one macrospore. The prothallium is green, and elongated, but slightly from the germinal axis. The sporangia are of two kinds (sex), which are either enclosed by an indusium, or enveloped in a portion of a leaf, to form "fruits" termed sporocarps. + +The old name for the Hygropteridaceae, "Bisconcerum," i.e. the "root-fruited," originated from the erroneous supposition that the sporangia were borne on the roots. + +Sub-Class 1. *Filices* (the True Ferns). +Of the eight orders (with about 4,000 species) comprised in this sub-class, the Polypodiaceae is the largest (having about 2,800 species) and the most familiar; for this reason it will be taken as typical. + +The sexual generation. When the spore germinates, the ectodermal cell divides to form a prothallus with a single leaf. The internal cell-wall (endosperm) grows out as a filament, which soon divides and gives rise to the prothallium, a flat, cellular expansion resembling the thallus of a Liverwort. In its fully developed state + +206 + +**Pteridophyta.** + +the prothallium is generally heart-shaped, dark green, and pre- +vided with root-hairs, and it attains a diameter of about one centimetre (Fig. +205). It is formed of one layer of cells, +except along the central line near the middle, where it is thickened by some +several layers of cells in thickness, +forming the "cushion," on the lower side +of which the archegonia are developed. +The prothallia are very variable; they +are thus found on the oldest parts of the +prothallium, on its edge, or among the +root-hairs. The archegonia are developed +in two forms, according to their position: +the apex. Several tropical Ferns have pro- +thallia deviating from this typical form; +*Ferocampus* (Order *Hymenophyllaceae*) +and *Ferocampus* (Order *Hymenophyllaceae*) +which resemble the protonema of a Moss. + +Others, again, have strap-shaped prothallia, which resemble the +thallus of certain Liverworts. + + +A small illustration showing a prothallium with archegonia. + + +**Fig. 205.—Prothallium (part of) Madura-fern (Maidenhair-silk). +semis.) with a young plant attached to it. A, prothallium; B, shoot; C, root; D, adventitious roots; E, k. h. +root-hairs; F, the prothallium apex. + + +**Fig. 206.—Authorities of *Madura-fern* (see 205). A, Urnips; B, rips; B unopened; C opened and dead; D, young plant attached to prothallium; E, young plant attached to prothallium closed in their mother-otio; the others are enclosed up and drug with them the epiphyllous +resinum.** +In the Polypodiaceae universal prothallia as distinct as those of *Equisetum* are of common occurrence. + +1 + +**PSEUDOPHYTA.** 207 + +The *archegonia* have been already mentioned (p. 190, Fig. 201). The *antheridia* are hemispherical or slightly conical bodies (Fig. 206). They consist, as in the Mosses, of a wall formed by one layer of cells, and a central cavity containing two spermatogonial cells (A and B). The antheridia when ripe absorb water, and are ruptured, and the spirally-coiled spermatoida liberated (Fig. 206 S). The spermatoids have been observed to pass down the neck of the antheridium. + +The *asexual generation*. The first leaf, the "cotyledon," of the embryo developed from the oospore (Figs. 202, 205) is always small, and has a very simple shape. The leaves which occur on the stem after the first leaf are all similar in form. A permanent form of leaf has been attained.--The stem is most frequently a subterranean or a semi-terrestrial; it is only in the tropical, palm-like Tree-Ferns, that the stem raises itself high in the air and reaches the surface of the ground, with leaves having no remains of leaves attached (Figs. 207, 203); in certain species it is en- +cased in a thick crust of aerial roots (*Dicksonia antarctica*). When the rhizome is horizontal the internodes are frequently elongated, and the leaves are arranged in two rows, while in *Bracken Fern* (*Pteridium aquilinum*) and in the *Bracken Fern* (*Pteridium esculentum*) etc., it is also generally *dorsoventral*, having a dorsal side on which the leaves are situated, and a ventral side, different from the former, on which the roots are borne. When these elements are in an oblique direction, as in *Duckweed* (*Lemna*), their internodes are short and thickened, and the leaves are arranged in a spiral line with a complicated phyllotaxis, e.g. in *Alisma filiforme*, *Ampelis filiformis*, etc. The meristematic region of the stem is usually confined to the petiole (e.g. *Agathidium*, *Riccia*), or to the base near the insertion of the leaves. Several species normally form buds on different parts of the lamina. The buds which are formed on the stem are not confined to the leaf-sass as in the higher plants. + +The *vascular bundles* are concentric, with the wood surrounded by the soft bast. In transverse section they are seen as circles or irregularly-shaped figures (Fig. 205), the name of "King Charles" and its derivatives being derived from this peculiar appearance, since the bundles present in oblique section. In *Onoclea* they are collateral and resemble those of the Flowering-plants. Round each individual bundle is often a sheath of thick-walled, hard brown, sclerenchymatous cells, which act as a mechanical w. n. + +A diagram showing the structure of a plant's vascular system. + +208 +PTERIDOPHYTA. + +tissue; similar strands are also found in other parts of the stem. +The leaves in nearly all species are only foliage-leaves, borne + +A large illustration of a tree with a thick trunk and numerous branches, with roots spreading out at the base. The leaves are long and narrow, resembling those of ferns. +Fig. 307. --Various Forms (1, 2, 3, 4). + +in a spiral. They have an apical growth which continues for a long time, and some require several years for their complete development. In the buds they are rolled up (erectate); not only the midrib, but also all the lateral veins, and even the terminal + +**Pteridophyta.** + +209 + +portions of a leaf are sometimes rolled up together, the tissues of the leaf being already fully developed and only waiting to expand. The leaves are often extremely pinnate and compound, with pinnate branches, and have an epidermis with stomata and a well-developed system of venation. Stipules are only found in *Marat- +taceae* and *Ophioglossaceae*. + +Very few leaves have scales or scales (pulver, pulvus), dry, brown, flat and broad, are found on stem and leaf. + +The *soriangia* are small, round capsules, which, in a very large number of ferns, are formed on the back, but more rarely on the edge of the leaf. In some species, such as *Polypodium*, there is any difference in form between the barrens foliage-leaves and the fertile leaves, as is found for example in *Blechnum* *spicant* or *Struthiopteris* ; or that the fertile part of the leaf is differently constituted from the barren portion of the same leaf, as in the *Royal-Fern* (*Onosma*) in which the mesophyll of the fertile part is poorly developed. + +The sporangia in the *Polypodiaceae* are lens-shaped, with long stalks (fig. 38). The sporangium is a hollow sac, within which a single row of cells, passing vertically over the top (that is along the edge of the sporangium), is developed into the "ring" (annu- +lus). The cells of the annulus are very much thickened on the inner side. The outer wall of these cells is thin. The thickened cells, however, do not entirely encircle the sporangium, but on one side, near the stalk, they pass over into large, flat, thin-walled cells. These form a weak point in the wall, and it is here that the sporangium is torn open by the pressure of its contents when the annular ring of bursting of the Polypodiaceae opens as it dries. The cells of the annulus are very hygroscopic, and in straighten- +ing, the annulus bands back with a jerk, thus ejecting the spores to considerable distance. The outer cells of the annulus are water- +with greenish tinge. [The sporangium appears as a single epi- +dermal cell, from which a basal stalk is cut off. Three oblique cell-walls, intersecting near the base, are next formed in the upper cell, and two transverse cell-walls are formed at the free surface; as in fig. 38.] The outer cell enclosed by four other walls is formed, the outer cells become the wall of the sporangium, while the inner cell, by a series of walls, parallel to its sides, cuts off a layer of cells constituting the "archesporium," and this archesporium remains behind. The spores are either oblong and bilateral, or they are tetra- + +210 +Pteridophyta. +hedric with curved sides, depending upon the way in which the +tetrad division has taken place. +The sporangia are almost always situated on the nerves and +gatherings of the leaves, which differ in form in the various +genera. The sort, in many genera, may be covered by a scale-like +structure, the *sulzura* (Figs. 211 B, 212). +In the majority of cases, each aera is situated on a small +papilla, and is surrounded by a short stalk, called the *sporangial +bundle*. Between the sporangia, hairs (*parozymes*) are often +situated, which spring either from the placenta or from the stalks of +the sporangia. +**Systematic Division.** The Ferns may be divided into two +groups, characterized by the structure and development of the +sporangia. The sporangia in the *Equisetophyta* take their origin +from a group of epidermal cells, and their walls are formed by +several layers of cells. In the *Polypodiophyta* (and *Lycophyta*) +hypocotylar terminal cell of the axial row of cells which gives rise to the sporangium. In the *Leytorophyta* the sporangia are developed from single epidermal cells, and their walls are uni- +layered. The echinocystis is a single epidermal cell, from which sixteen spore-mother-cells are developed. It is diffi- +cult to say which form is the oldest (according to Prantl, those +which have the sort on the nerve-ending); however, the Equisen- +gium would seem to have marked their appearance before the +others. It also well defines *Marattia* and *Ophioglossum*. +About 4,000 species of Ferns are now existing, and they are +found especially in tropical and temperate regions. +Family: *Euphorangiaceae.* +Order 1. Ophioglossaceae. The prothallus differs from that of all other Ferns in being subterranean, free from chlorophyll, +pale and tuberosa. The stem is extremely short, with short internodes, and is usually completely buried in the ground (Fig. 208 a). In several species (among +which are the native ones) one leaf is produced every year, which has taken three to four years for its development. In *Bryog- +ium* a closed, imbricated leaf is produced at each node, which +separates itself during their development. In *Ophioglossum*, at +the position of the axillary axils are different in the various orders: longitudinal in *Polypodium*, transverse in *Cystopteris*, immersed in *Dio- +seos*, Gleichenia; indolent or immed in *Cordifolia*, *Cystopteris*, *Marattia*, *Salvinia*, *Marvisianum*. + +A diagram showing the structure of a fern spore-producing cell. + +Pteridophyta. 211 + +others each leaf has at its base an interpetiolar, cap-like sheath, which protects the succeeding leaf. The leaves are of two kinds: +(a) foliage, which in *Ophioglossum vulgatum* are lanceolate and entire, but in *Botrychium* however, are pinnae (b in Fig. 208 A, B); and (b) fertile, which are found facing the upper side of + + +A: A leaf with a sheath. +B: A pinna. +C: A pinna with a sheath. +D: A pinna with a sheath. +E: A pinna with a sheath. +F: A pinna with a sheath. +G: A pinna with a sheath. +H: A pinna with a sheath. +I: A pinna with a sheath. +J: A pinna with a sheath. +K: A pinna with a sheath. +L: A pinna with a sheath. +M: A pinna with a sheath. +N: A pinna with a sheath. +O: A pinna with a sheath. +P: A pinna with a sheath. +Q: A pinna with a sheath. +R: A pinna with a sheath. +S: A pinna with a sheath. +T: A pinna with a sheath. +U: A pinna with a sheath. +V: A pinna with a sheath. +W: A pinna with a sheath. +X: A pinna with a sheath. +Y: A pinna with a sheath. +Z: A pinna with a sheath. +AA: A pinna with a sheath. +AB: A pinna with a sheath. +AC: A pinna with a sheath. +AD: A pinna with a sheath. +AE: A pinna with a sheath. +AF: A pinna with a sheath. +AG: A pinna with a sheath. +AH: A pinna with a sheath. +AI: A pinna with a sheath. +AJ: A pinna with a sheath. +AK: A pinna with a sheath. +AL: A pinna with a sheath. +AM: A pinna with a sheath. +AN: A pinna with a sheath. +AO: A pinna with a sheath. +AP: A pinna with a sheath. +AQ: A pinna with a sheath. +AR: A pinna with a sheath. +AS: A pinna with a sheath. +AT: A pinna with a sheath. +AU: A pinna with a sheath. +AV: A pinna with a sheath. +AW: A pinna with a sheath. +AX: A pinna with a sheath. +AY: A pinna with a sheath. +AZ: A pinna with a sheath. +BA: A fertile leaf, showing sporangia on the underside of the leaf blade. The sporangia are placed laterally, and open by two valves. No annulus is formed (Fig. 209). +\textit{Ophioglossum} reproduces vegetatively by adventitious buds on the roots. + +Fig. 208.—(a, b.) lanceolate umbonae (folio-ventricose). Botrychium, lanceol (lance-woed), both natural size ; rev. under ; to left-hand ; to right-hand ; fertile leaf. + +the foliage-leaves. These latter in *Ophioglossum* are undivided and spike-like (Fig. 209 A), but pinnate in *Botrychium* (Fig. 208 E). + +Each fertile leaf bears one or more sporangia on its underside. The large sporangia are placed laterally, and open by two valves. No annulus is formed (Fig. 209). *Ophioglossum* reproduces vegetatively by adventitious buds on the roots. + + +A fertile leaf of *Ophioglossum.* + + +313 +FLEXIDOPHYTA + +Three genera with about twelve species. + +Order 2. *Marantaceae* are tropical *Ferns*, whose gigantic leaves resemble those of the Polypodiaceae, but have stipules in addition. The sporangia are grouped in sori, situated on the lower side of the leaves, the sporangia in each sori being arranged either in a single row (Fig. 210 A), or in two rows (Fig. 210 B), or in three rows (Fig. 210 C). In *Maranta* and *Kunia*, as well as in *Dimeria* (Fig. 210 A), but in the other species (*Kunia*, *Dimeria*, *Maranta*), they are united, and form "syngania" divided into a number of chambers corresponding to the sporangia. These open by clefts or pores, and contain numerous spores. In *Maranta*, its sporangia are completely united in a cap-like-ly ancyranum, which is closed until maturity, and then opens by two valves. +In each valve there is a row of three to eleven sporangia, each opening by a slit towards the outside (Fig. 210 B); the sporangia enclosed within the ancyranum except in *Kunia*; the ancyranum is formed of flat and loiled hairs, which resemble the hairs of the other portions of the leaves. In *Angiopteris* and *Maranta* the indusium is very rudimental; in *Dimeria* it forms a kind of cupula. + +A + +The numerous fossil Marantaceae (5 genera, with 98 species) present almost exclusively in the Trias, but more various forms are found, for example, with military fire sporangia. These are found in the Permian remnant (4 genera with only 23 species) of a once dominant family, which was at one time very important, and whose culminating point was reached in the Kulm and Coal periods, and which has been replaced by the *Polypodiaceae* in the Kulm and Coal periods, and were short-lived compared with the present species). Leptosporangiote *Ferns* appear however to have covered half of all the Trias-formation. + +Family 2. *Leptosporangiatae.* + +Order 1. *Polypodiaceae.* Sporangia on the lower side of the leaves, **x**illed and provided with a vertical, incomplete annulus; dichotomous by a transverse cleft (Fig. 211 D). The genera are distinguished by the form of the indusium and the position of the sori, etc. + +Fig. 210.—Sporangia of the Marantaceae. +A. Single row. +B. Two rows. +C. Three rows. +A diagram showing the arrangement of sporangia in a single row (A), two rows (B), and three rows (C). + +8 + +**Pteridophyta.** + +213 + +1. The sporangia cover the entire lower surface of the leaf (Tropical America and Asia). *Acerolatium*, *Patagium*. + +2. Sori without indusium, circular or oval. *Polypodium* (Fig. 211 A). The leaves are most frequently situated in two rows on the terminal branchlets, and are covered with a smooth scar behind.--*P. vulgare*, common in woods, on stones. (*Phyto- pteris* also has no indusium; see page 214). + +3. The sporangia are situated in continuous lines just inside the margin of the leaf, so that the lines form a continuous line along the entire margin of the leaf (Fig. 211 C), which bends over and covers the sporangia, forming a "false-indusium". *Pteridium* has linear sort situated on a marginal vascular bundle, covered by two linear basal indusia, of which the outer is bent over like the edge of a tent--*P. aquilinum* (Brockman) has a wide spreading + + +A I +B J +C K +D L + + +Fig. 211.--Portions of leaves with sorus. *A* Polypodium. *B* Juglans. *C* Pteridium. *D* Asplenium. *E* Pteridium. *F* Pteridium. *G* Pteridium. *H* Pteridium. *I* Pteridium. *J* Pteridium. *K* Pteridium. *L* Pteridium. + +rhizome with large alternate leaves, placed on opposite sides, at some distance apart. Only one leaf is developed from each branch every year. + +*Adiantum* (Maiden-hair): sori on the underside of small portions of the edge of the leaf, which are bent over false indusia. *Cyperoëraea* (Lemmeru), *Chelanthaceae.* + +4. The sort are oval or linear, situated on one side of the vane, but not covering it completely (Fig. 211 A). They are linear indusia with one of its edges attached at the external side.--*A. rutus narra- rius* (Wall-Roe); *A. septentrionale; A. trichomanes.*--Althymus: sort linear or curved.--*A. filix-femina* (Lady's-Fern). --Scopulendrium. + +5 The former genus *Pteris* is divided into *Pteris* and *Pteridium.* + +--- +The former genus *Pteris* is divided into *Pteris* and *Pteridium.* + +214 + +**Pteridophyta.** + +(Fig. 212 B) : sori as in *Asplenium*, but situated in pairs across the lanceolate, entire leaves. Each sori is covered on the ex- +ternal side by an indusium, whose free edges are parallel and ap- +proach each other. *S. vulgare* (Hart's-tongue).—*Dichaea* (E. opeanit, +Hart's-tongue).—*Polypodium* (Wood's-pine).—*Polytrichum* (Broom- +grass), while the underside is almost entirely covered with sori, and hence they are of +a different nature from those of the leaves. —*Lecanora* : indusium. +5. Sori circular and covered by a shield-like, or reniform +indusium.—*Aspidium* (Fig. 211 B); the leaves without any and leave no scar upon the leaf-stalks. —*Cystopteris* (Male-Fern); a. +*Cystopteris montana*. The indusium has no indusium, the whole base of the leaf-stalks are persistent ; *P. argyrospora* and *P. polytrichoides*. + +The indusium is situated below the sori, and has the shape of +a one-sided scale (*Cystopteris*, *Steliopteris*), or of a cup or cupule, +which in *Wood's pine* is sometimes rimless (Fig. 36 C, D). + +A: A single sorus of the male fern. +B: A single sorus of the female fern. +C: A single sorus of the wood's pine. +D: A single sorus of the male fern. +E: A single sorus of the wood's pine. + +Fig. 211.—A *Asplenium*, B *Polypodium*, C *Wood's pine*, 2 single sori of the same. +E *Cystopteris*, the spores have fallen off, leaving only the indusium. + +7. The sori are situated on the margin of the leaf, and at the end of a vascular bundle. Indusium, semi-cupular. *Duralias*. Principally tropical and subtropical. + +This order is the greatest, comprising about 2800 species, the majority being perennial plants. A few are large, and known as +Tree-Form. + +As plants in conservatories and rooms the following are cultivated : species of +*Asplenium* (topical), *Lemnaceae*, *Nephrolepis*, *Pittosporum* (F. serratum, cretice). + +Officinal. *Asplenium filix-mas*, elate-moss and this withered plantain.—Species of +*Lycopodium*, *Lycopodium clavatum*, *Lycopodium annotinum*. Species of +*Athyrium*, *Athyrium filix-femina*, *Athyrium crenulatum*. Species of +*Polypodium*, var. *cerealeum*, contains so much starch that it is used as food. +The other orders of true Ferns deviate from the Polypodiaceae, especially in + +**PTERIDOPHYTA.** + +the formation of the annulus, the bursting of the sporangium and its mode of attachment and development, and in the differences in the formation of the prothallium. + +Order 3. Hymenophylaceae. +To this order belong the lowest and most Mass-like Ferns; the leaves, with the exception of the veins, are most frequently forked, and the sporangia are attached to the leaf by a stalk. The prothallium, the formation of the prothallium also somewhat resembles the Mosses. Sori marginal, on the extremities of the scaleular bundles, and surrounded by a cupule, which is often very large. The leaves are usually simple, but sometimes compound (Fig. 251). *Typhosporum* (It., tumbulare, European), *Trichomanes* (T., spectaculum, Euro.), *Eurosporium* (Sp., species about 200, which live chiefly on rocks and trees in damp soil and on stones). + +Order 4. Cystaceae. +Annuals complete and oblique. To this order be long, principally the tree-ferns, and are mostly hard. The number of scales in each leaf is not always equal, and forms vary in different regions. *Cystopteris* and *Dicranopteris* have marginal sori, with epimera; basal indusium. (The stem of $L$. serrata is covered with aerial roots.) *Mnephila* (without Indusium); *Cystopteris* with epimera; *Heterotrichium* (Fig. 252). + +A +B + +Fig. 251.—Gleichenia: A part of a leaf with sorus; B is a single sorus. + +Order 5. Gleicheniaceae. +Sporangia with equatorial annules, and longitudinal dimidians, more frequently groups of 3-4 in sorus without indusium (Fig. 253). Diffuse or pinnate-leaved plants, with long petioles. + +Order 6. Schizomycetaceae. +Annelas apical. To this order belongs *Austrotyphlops*, a plant with long petioles, which is a member of the fern family. The leaves are metamorphosed, having no leaf-parenchyma and being covered with sporangia. *Schizomys*. *Lycopodium*, a climber, whose leaves have unlimited growth and are covered with sporangia. + +Order 7. Osmundaceae. +The sporangia have at the apex a lateral group of strongly thickened cells, which gradually pass over into the ordinary cells. The sporangia are attached to the leaf by a stalk. Leaves bear the sporangia upon peculiar, branched pinnae, without epimera (the uppermost in the leaf). *O. regalis* (Regal-Fern); European. + +Sub-Class 2. Hydropteridaceae (formerly Rhizocarpaceae). +Water Ferns. + +The following further characteristics must be added to those given on page 205: + +215 + +216 +**Pteridophyta.** + +Sexual generation. The *micropores* produce an extremely rudimentary prothallium, formed of only two cells, and having + +A microsporangium with germinating microspores and pre-germinating zygotes (a). A prothallium (b) with two cells (c), one of which has produced a new prothallium (d). A prothallium (e) with two cells (f), one of which has produced a new prothallium (g). A prothallium (h) with two cells (i), one of which has produced a new prothallium (j). A prothallium (k) with two cells (l), one of which has produced a new prothallium (m). A prothallium (n) with two cells (o), one of which has produced a new prothallium (p). + +Fig. 211.—Salvinia natans. A microsporangium with germinating microspores and pre-germinating zygotes (a). B a prothallium with two cells (b), one of which has produced a new prothallium (c). C the two cells of the antheridium have opened by transverse walls, and the spermatids are enclosed by the antheridial membrane. D spermatids still enclosed in the mother-cell. + +also a very much reduced bicellular antheridium with a small number of spermatoid mother-cells in each cell (in *Salvinia* 4, in *Maraisia* and *Philodra* 16). In *Salvinia* the microspores remain embedded in a hard multicellular mass (at first freely) which fills up the cavity of the sporangium. The prothallium mass therefore + +A prothallium with two cells, one of which has produced a new prothallium. + +Fig. 212.—Salvinia natans. A, B Fructus probabile, $F_2$, protruding from the microsporangium while in the process of germination. C, D Prothallium, $F_3$, with two cells, one of which has produced a new prothallium. E, F Prothallium, $F_4$, with two cells, one of which has produced a new prothallium. G, H Prothallium, $F_5$, with two cells, one of which has produced a new prothallium. I, J Prothallium, $F_6$, with two cells, one of which has produced a new prothallium. K, L Prothallium, $F_7$, with two cells, one of which has produced a new prothallium. M, N Prothallium, $F_8$, with two cells, one of which has produced a new prothallium. O, P Prothallium, $F_9$, with two cells, one of which has produced a new prothallium. Q, R Prothallium, $F_{10}$, with two cells, one of which has produced a new prothallium. S, T Prothallium, $F_{11}$, with two cells, one of which has produced a new prothallium. U, V Prothallium, $F_{12}$, with two cells, one of which has produced a new prothallium. W, X Prothallium, $F_{13}$, with two cells, one of which has produced a new prothallium. Y, Z Prothallium, $F_{14}$, with two cells, one of which has produced a new prothallium. A like lobes of the prothallium ; m the foot. + +PTERIDOPHYTA. +217 + +grow out through this slime and also through the wall of the sporangium (Fig. 215), and it thus terminates in a relatively long cell. + +In *Marilia* the microspores are set free from the microsporangium, and the prothallus, with the archegonia, remain in them until their contents are liberated. The latter are spirally twisted threads. + +The macrospores, on germination, give rise to a very reduced prothallium, which in *Sauritia* bears 3 archegonia; but, if these are not formed, the prothallus is completely reduced to a fairly large leafy body with several archegonia (Fig. 215 A, B). In *Marilia* the prothallium is still more reduced, it is enclosed in the macrospore, and only bears one archegonium. The archegonia + +A diagram showing the structure of a plant with two archegonia. +B A diagram showing the structure of a plant with three archegonia. +C A diagram showing the structure of a plant with four archegonia. + +Fig. 215.—Diagrammatic views. A An archegonium, simple, seen in longitudinal section; b the neck-cells; c the neck-archegonium; d the central cell. E An open archegonium in which the neck-cells have separated off. F An open, old archegonium seen from the top. + +The asexual generation is developed from the fertilised egg-cell. It is a dorsoventral, horizontal shoot. In *Sauritia* it bears at first a shield-like leaf, the scutiform leaf (Fig. 215 C a), which is succeeded by the ordinary foliole-leave. The young plants of *Marilia*, likewise, have less perfect leaves in the very early stage. + +The formation of the sporangium is the same as in the Leptocarpophyta (p. 608) (the tetrahedral cells originate from one central, tetrahedral archesporium.). + +The Hydropteridae are divided into 2 orders, the chief differences between them being found in the asexual generation. + +218 +PTERIDOPHYTA. +Order 1. **Salvinia**æ. This order more nearly approaches the true Ferns, especially so on account of the form of the indusium. + +A diagram showing the roots of Salvinia natans, with one root above, floating on the water, and a portion of another root below in its natural position in the water. +Fig. 317.—*Salvinia natans* (natural size). A. root near shore, floating on the water; B. portion of root taken up in its natural position in the water. + +Only one species is found in Europe, *Salvinia natans* (Fig. 217). +This is a small, floating, annual, aquatic plant, entirely destitute of roots. The dorsoventral, horizontal stem bears two kinds of leaves, which are arranged in whorls of three. Two of these which turn upwards are oval, entire, "narrow-ovate" (Fig. 217, $a$), the third, the "outer-leaf" ($b$) is submerged and divided into a number of hair-like segments, similar to those of the leaves in many aquatic plants, for instance, Water-buttercup (see also Fig. 215 C). The whorls of leaves continue with three leaves; there are thus four rows of dorsally-placed aerial leaves, and two rows of ventrally-placed submerged leaves. +The indusium is a column (receptacle or placenta) and enveloped by a cupular, but entirely closed indusium (Fig. 218). The sori are situated on + +A diagram showing the structure of *Salvinia natans*. A shows the stem with three leaves; B shows the internal structure of the stem with a cross-section through the middle leaf showing the vascular bundles; C shows a magnified view of one of the leaves showing the venation; D shows a magnified view of one of the leaves showing the stomata. +Fig. 218.—Root of *Salvinia* in longitudiunal section (natural size); $a$, macrosporangia. (x 10.) + +PIERIDOPHYTA. +219 + +the submerged leaves (Fig. 217, B, e-v) and are unisexual, i.e. each sora contains microsporangium only, or macrosporangium. + +*Ovalia* belongs to this order. It is a very small, floating, tropical water-plant (America and East India), with horizontal, root-bearing stem. The stem branches profusely, and the leaves are arranged in two rows on the upper side, and one row on the ventral side. Each leaf is bifid, and divided into an upper domal, and a lower ventral portion. The upper segments float on the surface of the water and are called *pulmonaria*, while the lower ones sink below. In each floating segment a large cavity is found, in which *xanthus* is always present. The lower segments are submerged. + +Order 2. *Marliaceae*. The characteristic feature of this order, and one not possessed by other Fern-like plants, is that the sori (Gametangia) are enveloped in a sporophyllous envelope which closes round these and form a "sporocarp," just in the same manner as the carpels, in the Angiosperms. The sporophylls are oval-shaped and the ovaules and form ovaries. The sori contain both micro- and macro-sporangia. When the spores are ripe, the sporocarp opens in order to disperse the spores (Fig. 220). + +The two genera (with 57 species, Temperate, Tropical) are land-and marsh-plants, plantains-like in their habit. Both bear roots on the under surface, and the leaves in two rows on the upper side (Figs. 219, 221). The leaves of *Marilia* are compound, with three to five small leaflets springing from the apex of the petiole (Fig. 219), and resemble the leaves of *Ovalia*. In the bud the leaves are circular (Fig. 219 b), and at night they exhibit the well-known peristaltic movements. The sporocarps are borne on the petioles of the fertile leaves, near their bases (Fig. 219 f); they are oblong and rounded at the base, being hard and silvery-margined, while the inner ones are divided into a number of loculi arranged in two rows. On + +A small illustration showing a plant with compound leaves. +(Fig. 218.) — *Marilia salutatrix* (after *Baker*). — *Ovalia* (after *Baker*). — *f.* sporocarpus; *a* point of branching of petiole. + +Order 3. *Hymenophyllaceae*. This order includes only one genus, *Hymenophyllum*, with about 60 species, all tropical or subtropical. The leaves are simple or compound, with several leaflets; they are usually pinnate or bipinnate; they have a long petiole; they are attached to a short rhizome; they are often covered with a sheath; they are usually deciduous; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral veins; they have a midrib with lateral veins; they have a central vein with lateral ven + +220 +PTERIDOPHYLLA. +germination, water is absorbed, the two sides separate slightly, as valves (Fig. 220 A), and a long vermiform mass of gelatinous, parenchymatous cells (Fig. 220), swollen with the water, emerges, bearing, beside each other, two leaves (Fig. 220 B). The stoma (er) is covered by a thin indusium. (The thin covering may be considered an indusium physiologically, though not morphologically). +*Marilia quadrifolia*, in Europe. Many species are found in Australia. The + + +A: A small, elongated structure with a central cavity. +B: A larger, more complex structure with multiple smaller structures attached. +C: A third structure, possibly representing a different stage or species. +D: A fourth structure, possibly representing another species or stage. +E: A fifth structure, possibly representing yet another species or stage. +F: A sixth structure, possibly representing a different species or stage. +G: A seventh structure, possibly representing a different species or stage. +H: An eighth structure, possibly representing a different species or stage. +I: An ninth structure, possibly representing a different species or stage. +J: An tenth structure, possibly representing a different species or stage. +K: An eleventh structure, possibly representing a different species or stage. +L: An twelfth structure, possibly representing a different species or stage. +M: An thirteenth structure, possibly representing a different species or stage. +N: An fourteenth structure, possibly representing a different species or stage. +O: An fifteenth structure, possibly representing a different species or stage. +P: An sixteenth structure, possibly representing a different species or stage. +Q: An seventeenth structure, possibly representing a different species or stage. +R: An eighteenth structure, possibly representing a different species or stage. +S: An nineteenth structure, possibly representing a different species or stage. +T: An twentieth structure, possibly representing a different species or stage. +U: An twenty-first structure, possibly representing a different species or stage. +V: An twenty-second structure, possibly representing a different species or stage. +W: An twenty-third structure, possibly representing a different species or stage. +X: An twenty-fourth structure, possibly representing a different species or stage. +Y: An twenty-fifth structure, possibly representing a different species or stage. +Z: An twenty-sixth structure, possibly representing a different species or stage. +AA: A small leaf-like structure. +BB: A larger leaf-like structure. +CC: A third leaf-like structure. +DD: A fourth leaf-like structure. +EE: A fifth leaf-like structure. +FF: A sixth leaf-like structure. +GG: A seventh leaf-like structure. +HH: A eighth leaf-like structure. +II: A ninth leaf-like structure. +JJ: A tenth leaf-like structure. +KK: An eleventh leaf-like structure. +LL: A twelfth leaf-like structure. +MM: A thirteenth leaf-like structure. +NN: A fourteenth leaf-like structure. +OO: A fifteenth leaf-like structure. +PP: A sixteenth leaf-like structure. +QQ: A seventeenth leaf-like structure. +RR: An eighteenth leaf-like structure. +SS: A nineteenth leaf-like structure. +TT: A twentieth leaf-like structure. +UU: A twenty-first leaf-like structure. +VV: A twenty-second leaf-like structure. +WW: A twenty-third leaf-like structure. +XX: A twenty-fourth leaf-like structure. +YY: A twenty-fifth leaf-like structure. +ZZ: A twenty-sixth leaf-like structure. + +Fig. 220—*Marilia quadrifolia*: At the young stage of germination. B shows the more advanced stage of germination. + +Fig. 221—*Ptilaria platyloides* (general view): The young plant. b—stem; c—leaves; d—stomata; e—the growing point; r—root. + +Nutritive sporangia of *Ml. quadrifolia* were the means of saving the Burke expedition in the interior of Australia, and hence this species has earned its specific name. + +*Ptilaria* has linear leaves, without lamina. The sporangia are spheroid (Fig. 221), brown and hard, situated near the base of the leaves. They are 2–4 chambered and open by a corresponding number of valves. + +14 + +PTERIDOPHYTA. +221 + +Class 2. Equisetinae (Horsetails.) + +The characteristics of this class have been described on page 204. + +It is divided into two sub-classes --- +1. The Isosporous Equisetum. To this sub-class belong, with certainty, only the Equisetum now existing, which are represented by only one genus, *Equisetum*. +2. The Heterosporous Equisetum. Forms which are now extinct. + +Sub-Class 1. Isosporous Equisetum. + +Order. Equisetaeum (Horsetails). +The sexual generation. +The prothallium is green and leaf-like, as in the majority of Ferns, but irregularly branched and curled. It is often unisexual. The male prothallium bears antheridia only, and are smaller and less branched (Fig. 222 A) than the female; the latter may attain a diameter of $\frac{1}{4}$ inch, and bear archelegonia only (Fig. 222 B). The antheridium and the archelegonia resemble those of the Ferns, but the spermatoids (Fig. 223) are + + +A: A close-up view of a green, leaf-like structure with irregular branches. +B: A diagrammatic illustration showing the structure of an antheridium and archelegonia. + + +Fig. 221.--*Equisetum arvense*. The prothallium highly magnified. +Fig. 222.--*Equisetum variegatum*. Male prothallium; $a$ male gametophyte; $b$ female gametophyte; $c$ archelegonia; $d$ earthen cells still enveloped in the prothallium. +Fig. 223.--*Equisetum variegatum*. Spermatoids. + + +222 +STEREODHYTIA. + +larger and less twisted. On the last curve is situated a more or less elongated appendage of cytoplasm (Fig. 223 c). + +The asexual generation. The embryo is similar to that of the Fornia. The fully developed *Epicotus* is a perennial herb, with widely spreading, simple or branched rhizomes, from which extend erect, aerial, most frequently annual shoots. + +The vegetative aerial stems are divided into a number of internodes by the whorls of leaves (Fig. 224). The internodes are hollow, the cavities being separated from each other by the transverse partitions of the solid nodes. The lower portion of the internode, which is enclosed by the leaves, has much thinner and softer cell-walls, so that it can be easily torn away at any point between the nodes. Each internode has a large number of ridges and furrows, and bears at its apex a whorl of leaves whose number and position correspond to the ridges of the internode. As in the one of *Euphorbia*, the leaves are arranged in two rows, one above the other; the same arrangement is also found in the ridges on two successive internodes. In addition to the large air-cavity in the centre of each internode (the central cavity), a + + +A: A plant stem with a whorl of leaves. +B: A plant stem with a whorl of leaves. +C: A plant stem with a whorl of leaves. +D: A plant stem with a whorl of leaves. + + +Fig. 224.—*Epicotus aureus*. A: a fertile branch with one b vegetative shoot; c: one; d: sporophyte. + +**PEREIDOPHYTA** + +223 + +whorl of tubular-air-passages is found in the cortex of the stems, opposite the furcules (valvular canal). There is also a similar air-passage (carnial canal) in each of the vascular bundles, which are placed in two groups of three, one group being placed altern- +ating with the valvular canals. The vascular bundles are col- +lateral as in the majority of Flowering-plants, but poorly deve- +loped. The xylem of each bundle consists of two groups of +annular or spiral vessels, and the phloem is composed of the carinal canal, and two groups of scalariform tracheids, one of which on a +radius passing through a group of spiral vessels. The phloem is +placed between these four groups, each of which has only a few +veeeds. The starch-grains are mainly due to the large +amount of starch in the cell-walls of the epidermis, and to the +sclereohymnous cells of the ridges. + +All leaves are situated in whorls. The leaf-attive is simple, +undivided, and are so situated that they are opposite (Fig. +224, a). The bracts are deciduous, and the inflorescence specific (Fig. +224, b). The bracts break through the base of the leaf-shafts (Fig. +224 b), and generally alternate with the teeth (leaves). + +The **fertile leaves** (gerophyllae) are different from the barren ones. They are free, shield-like, each one having a short stalk +bearing usually an hexagonal plate (Fig. 224 d), and closely com- +pressed into an eno or cone (Fig. 225 c e). The Euplectra thus present +show that this is a very early stage in the formation of the +Ferns, which is further emphasized by the circumstance that a +transition from the sheath-leaves to the fertile-leaves is found in +the involucre or annulus, a "cotyl" of specially modified leaves +situated at the base of the sporophylls. This cotyl or young cone may be considered as a very rudimentary flower, and the annulus may be regarded as a very early stage in the formation of a flower +(perianth). See page 235. + +The sporophylls are green on the underside of the sporophylls, +one at each angle; they are sac-like, and open inwardly by a +longitudinal cleft (Fig. 224 d). An annulus is wanting; but in +the wall of the sporangium, as in the pollen-nests of the Flower- +ing-plants, a layer of thickened walls is developed. This thickening, +is developed, which assists in the deliquescence of the sporangium. + +The scales are green; the walls composed of three distinct +layers, of which the outer is gradually separated, except at one +point, and becomes split into four long bands (lateri) (Fig. 225). +W.t. + +224 +Pteridophyta. + +The elaters are extremely hygroscopic, coiling round the spore when moistened, and expanding as soon as dry, presenting a most lively object under the microscope when breathed upon and allowed to dry. The second layer, when germination commences, becomes detached from the inner wall, which is formed of the exosperm and endosperm. + +The order has become much reduced, and at the present time includes only one genus, *Equisetum*, with about twenty-five species, which are found in all parts of the world, but especially in damp situations. In some species the barren shoots are green and very much branched, but the fertile ones are unbranched, pale brown, and possess no chlorophyll (*E. arvense*, Field-Horsfall, Fig. 321), and in some species the fertile shoots are alike green, and either both unbranched (*E. hiemale*, or branched (*E. paucirame*, E. lemaneu, etc.). The fertile shoots of *E. villiciumm*, + +A diagram showing two types of equisetum shoots: A, a fertile shoot with elaters (a) coiled round the spore; B, a barren shoot. +Fig. 321.—Spores of *Equisetum*. A, fertile, with elaters (a) coiled round the spore; B, barren. +up to maturity, resemble those without chlorophyll of *E. arvense*, but after that period they produce green branches, and thus resemble the barren ones. + +Extraneous knowledge. In addition to several true species of *Equisetum*, there are many other plants which are closely allied to the Equisetum, is also found in the fossil state. These were giant forms, attaining about twenty times the size of those of the present day, and stems of considerable length. They attained their greatest developmen +titing point of their development in the Carboniferous period, and died out towards the close of the Paleozoic. The stems had hollow internodes and a branching system similar to that of *Equisetum*. The leaves must either have been absent or very perhable, since they have not been identified with certainty. If the determinations of certain remains of cones which of *Equisetum* are correct, then these plants must have possessed and had two kinds of sporangia as in the following sub-class. A cambium forma- +ted on the outside of the stem. + +Their uses are very limited. A few species, such as *E. hiemale* are used for polishing on account of the hard silicious cell-walls of the epidermis, found in all species of *Equisetum*. + +PTERIDOPHYTA. +225 + +Sub-Clas. 2. Heterosporous Equisetum. + +The two orders which come under this head are united by the characteristics, that the verticillate leaves are not united (Fig. 206), and that be- +tween each whorl of fertile leaves there is also a whorl of barren ones. The + +A fragment of Anaspidus. +Fig. 208.—A fragment of Anaspidus. + +Fertile whorls in Anaspidus are situated about midway between the barren ones (Fig. 207), but in Anaspidus longus they are considerably above a barren whorl (Fig. 228) and contain only half as many members as the latter. The lower whorl bears macrospores with one macropore, the upper, micro- +spore with many microspores. + +A fragment of Anaspidus longus. +Fig. 207.—Fragment of Anaspidus longus. + +The fertile whorls of Anaspidus longus are usually very large, and par- +tly fall off ; a barren whorl is a fer- +tile whorl. + +The ANASPIDS were dimorphic (Fig. 236), and presumably floating plants. +The Anaspids became extinct during the Carboniferous period, at the close of the Palæozoic. + +A fragment of Equisetum. +Fig. 208.—Fragment of cone of Adra- +phanta (Cretaceous Cretaceous); × 4 and × +3 in Fig. 237. + +The Equisetums were dimorphic (Fig. 236), and presumably floating plants. +The Equisetums became extinct during the Carboniferous period, at the close of the Palæozoic. + +226 +PTEXEDOFYTAL. + +Class 3. **Lycopodiæ** (Club-Mosses). + +The characteristics of this class have been given on page 205. +It consists of two sub-classes, one embracing isoporous, the other heteroporous forms. + +Sub-Class 1. **Lycopodiæ** (Isoporous Lycopodiæ). +One kind of spore. Prothallium large, partly green. Leaves without ligule. + +A detailed illustration of a lycopsid plant, showing its structure and parts. + +Fig. 228. — *Lycopodium annotinum*. A stem, with prothallium (gr.), one leaf, and a sporangium (s). B section through the prothallium (gr.). C section through the prothallium (gr.), showing the cells of the gametophyte. D a portion of a leaf, cut transversely in the place of the paper. + +Order 1. **Lycopodiaceæ**. The PROTHALLIUM is now known in nearly all the species; it is always more or less tubercular, and bears leaves at the summit. + +In *L. annotinum* the prothallium is a relatively large mass of cells, without chlorophyll, and subterranean, in which the anthocidia and aragononia are embedded (Fig. 229). In the widely distributed tropical species, *L. cerumen*, + +An illustration of a lycopsid plant's prothallium and gametophyte. + +**PEREIDOPHYTA.** + +227 + +and in *L. cordatum*, it is a small tubular body which has a subcercanum portion, with either little or no chlorophyll; and an aerial green portion. +The prothallus of *L. palghatense* and other live saprophytically in the ovaries of the fruit of trees; they are partly filamentous, branched, and possess no +chlorophyll. + +The asexual generation. **Perennial plants.** The stem branches monopodially (often apparently dichotomously), and is thickly covered by small, simple, triangular or cup-like leaves. The leaves are usually green, but in some species, such as *L. clematis*, and in others, whose stem is compressed with unequal sides, opposite (Fig. 231). The roots of *Lepidodendron* are dichotomously branched. + +The sporangia in *Lepidodendron* are situated singly at the base of the leaf, almost in their axils; they are reniform, unilocular and + +Lepidodendron cleistogenes. A lateral view from above, showing the sporangium and a strand of terminal spores still lying within the leaf. +Fig. 231. Lepidodendron cleistogenes. A lateral view from above, showing the sporangium and a strand of terminal spores still lying within the leaf. + +open like a mushroom-bell by two valves (Fig. 230 b). The sporangia are developed from a group of surface cells. The archesporium is formed from one hypodermal cell (or perhaps a cell-row). +The fertile leaves are collected upon definite regions of the stem. They are either all fertile or all barren; or the fertile portions of the stem pass gradually, without any break, into the barren portion (*L. selago*); or they differ from the barren leaves, and are then collected into special apical cones (Fig. 230 a). The ovules are produced in the ovaries (Fig. 230 b). + +About 100 species, chiefly tropical. + +Five species of *Lepidodendron* are found in Great Britain. *L. cleistogenes* and *L. selago* are common in mountainous districts. *L. anisomum* is common in the + +Lepidodendron cleistogenes. A lateral view from above, showing the sporangium and a strand of terminal spores still lying within the leaf. +Fig. 231. Lepidodendron cleistogenes. A lateral view from above, showing the sporangium and a strand of terminal spores still lying within the leaf. + +229 + +**PERIDIOPHYTA** + +Highlands of Scotland. The other genus of the order is *Phyllophlema*, with one species, *P. drummondii* (Kangaroo, Tasmania, and New Zealand), a small plant only a few centimeters high, with two leaves and about eleven linear leaves in the axils of which are numerous flowers borne by a cone of sporophylls. + +—Fossil Lycopodiaceae in the Carboniferous period. + +**ORIGINAL:** "Lycopodium," the spores of *L. clavatum* Family: Lycopsida. The leaves are simple, long, and the axis short, two- to three-leaved, as 3-8; seldom four, small capsules. Small herbs, with angular stem; leaves small, single, and one-nerved. Only four species—*Polypodium* (Mastigophora) and *Lycopodium* (Heterophora)—are known to have been plas- +ted supplied by special underground stems which bear a few modified leaves, +very much reduced, especially when buried deeply in the soil. Three species. +**Tropiophoræ (asteroid), one species.** + +Sub-Class: **Selaginellaceae** (HETEROPHORAE Lycopodiaceae). + +Micro- and macrospores. The prothallus are very much reduced, especially the male; the female does not involve the spore. The leaves are ligulate. + +A B C + +For 35.—Diagrammatic of the structure of *Selaginella*. A, the upper sporangium, +transverse, seen from above. In the interior see the prothallus (*A*), and the first +thread-like cell (*B*). The second thread-like cell (*C*) is seen at the base of the +sporangium-membrane formed in *C*. In the microspore is found the spermatangia +and the motile cells are surrounded by a mycelium. + +The sexual organs formed by the microspores are formed: +(1) a very small "vegetative" cell (fig in 229 A, B); and (2) +a cell many times larger (the antheridium) which divides into a number (4-8) of peripheral cells, enclosing 2-4 inner cells, which last form a large number of spermatangium-mother-cells in +*Nesotrichum* and *Equisetum*. On this stage where the +spore-wall is ruptured, the spermatangia and spermatangium-mother- +cells are ejected into the water. + +The spermatangia in *Selaginella* are elongated and club-shaped, +with two cells (Fig. 214); but in *Equisetum lacustris* they are annularly- +twisted threads which differ from all other spermatangia by + +STEREOPHYTUM. 220 + +having a bunch of cells at each end; the other species of *Inocles* have cells only at the anterior end. + +The macrospores. Shortly after the macrospores have been set free, or in *Sedumilla*, which is closed at the beginning of the mother-plant, they germinate and soon become filled with the cellular contents of the protuberance, and even in *Sedumilla* the first microsporogonia to be formed before the rupture of the spore-capsule has commenced (Fig. 235 A). + +The *archegonia* are constructed on the same plan as those of the + +A diagram showing the structure of an archegonium. + +Fig. 236.—Structure of *Sedumilla*. A triradiate archesporium, with the rupture of the wall six weeks after being formed. The endosperm (a) has not yet filled the entire chamber. Cell-formation still proceeding in the lower part of the thallus. The endosperm is seen in B, and C shows a section through it. D is a transverse section of a sporangium, with a spore seen from outside: a wall of the spore ; or archegonium. + +A diagram showing the structure of an archegonium. + +Fig. 237.—Archegonium of *Sedumilla*. A mature, in longitudinal section; c is the central cell ; a neck-canal, which is walled in between two terminal neck-cells. B rises ; a vertical section through it from above, open. It will be noticed that the neck is formed of two tiers of four cells each. + +A diagram showing the structure of an archegonium. + +Fig. 238.—Archegonium of *Sedumilla*. A mature, in longitudinal section; c is the central cell ; a neck-canal, which is walled in between two terminal neck-cells. B rises ; a vertical section through it from above, open. It will be noticed that the neck is formed of two tiers of four cells each. + +230 +PERIDIOHYMELA. + +other Arachnoïdinae, but are quite embedded in the prothallium (Fig. 235 = 230). +The asexual generation varies very much in the different orders. +Order I. Isotocaceae (Quill-worts). The only known genus, +Isotocia (Quill-woot), has an extremely short, tubercular, unbranched stem with very short internodes (Fig. 237). The stem is remarkable as being the only one among the Vascular Cryptogams which increases in thickness (see page 202). The meristomatic + + +A small illustration showing a plant structure with a central axis and branches. + + +Fig. 237.—Isotocia lacertae (slightly diminished) of the stem ; r rocka ; b leaves. + +Fig. 238.—Fecula lucidae (slightly diminished) of the stem ; r rocka ; b leaves. The stem is very short and with a narrow, convex edge of the groove, in which the microsporangium is placed, is continued as a thin dorso-ventrally flattened leaf. The inner edge of this leaf bears two to four macrosporangia, while the outer edge bears the microsporangia into compartments; i vacuole torus. + +Fig. 239.—Fecula lucidae (slightly diminished) of the stem ; r rocka ; b leaves. The stem is very short and with a narrow, convex edge of the groove, in which the microsporangium is placed, is continued as a thin dorso-ventrally flattened leaf. The inner edge of this leaf bears two to four macrosporangia, while the outer edge bears the microsporangia into compartments; i vacuole torus. + +The cells are flattened round the axial cylinder, and form, especially, parenchymatous cells in two to three directions, from which rise to 2–3 grooves in which the dichotomously-branched roots are produced. The leaves are arranged spirally in a close rosette. + +230 + +PTERIDOPHYTA. +231 + +They areawl-shapedandhaveatthebaseasemi-amplexusial +sheath,withagroove(fore),inwhichasporangiumissituated +(Fig. 258). The ligule is a foliar outgrowth from the upper edge +of the groove.—The macrosporangia (each with a number of +macrospores) are situated on the upper side of the sporangium +(Fig. 258), on the inner ones. Between each cycle of fertile +leaves there are a number of imperfect or barren ones, as in the +case of the female plant of Ophioglossum. The spores are liberated by the +dency of the sheath, which is opened at the base of the leaves at the commencement in the same way. The archesporium is, at first, a hypodermal layer of cells which grow out in the direction perpendicular to the surface of the leaf, and divide by a number of +walls producing two or more layers of cells. Some of the cell-rows of this sporogenous mass lose their +protodermal contents, and are arrested in their growth; thus +incomplete divisionsalve of sterile cells, "trabeculae," arise in the +sporangium, and these are separated from one another by spaces above +the other (Fig. 238 T). (The trabeculae, according to Goebel, play +the same part as the nutritive cells of the sporangium of Riolia; +the tapetal cells, as in the Ferns, are in a great measure dissolved at a later period.) The macrospores, in the micro- +sporangia, arise to a large number of sporogenous cells; but in the macrosporangia only one spermocyte-cell, with tapetum, +is developed from each fertile archesporial cell. + +The two native species of this several-celled genus are aquatic plants, +on the common occurrence land plants also are amphibious. About +50 species. In temperate and tropical regions.—Fossils species in the +Tertiary period. + +Order 2. Selaginellaceae. This order contains only one genus, +Selaginella. The stems are, in the majority of species, isoserial, +long and slender, and apparently branches dichotomously, but in +reality monopodialy, with well developed lateral shoots. The leaves are small, round, or ovate, in the majority of species arranged spirally around the stem; but in some species they are, +are not decussate, but are considerably inclined towards each other; an arrangement by which four rows of leaves are produced, +each having one large and one small leaf. The two leaves on each stem are usually opposite to each other; one is broad on the upper surface and the larger on the lower surface of the stem (Fig. 240). Some species have spirally-arranged leaves, much resembling the arrangement in the *Lycopodium*. + +A diagram showing a cross-section of a fern-like plant with sporangia and spores. + +232 +PIEZIDOFYTAL. + +The **fertile** leaves most frequently differ from the barren ones, and are collected into spike-like cones (a kind of flower: Fig. 250). Micro- and macro-spore-aragonia are found in the same cone (Fig. 250). +Each sporangium arises from a group of superficial cells of the stem, directly over the leaf on which it will be situated later on. +Each microsporangium consists of a single layer of epidermal cells, and contains a layer of tapetal cells; these are dissolved later, when the spores are ripe, and not before as in the Fera. In the very early stages of their development, the microspores and macropores are precisely similar, and the differences between them arise later on. In the mature sporangium all the spore-mother-cells divide, and each gives rise to tetra-hedrically-arranged microspores (Fig. 204); but in the macrosporangium only four macrospores are formed, by two divisions of one mother-cell, while the remaining seven spore-mother-cells are aborted. It is rarely that the macrosporangium contain 2 or 3 macrospores. + +Fig. 250.—Solepulpa marcescens. A fertile cone with microsporangia. + +For the elucidation of the theory see pages 228, 229. The prothallus arises in the macrospore (Fig. 7) in Fig. 253 c), probably by division of the mononuclear stage-prothallus mass, which is marked off at the apex of the spore; presumably this occurs within three weeks after sowing. + +In six to seven weeks after sowing, the outer-surface is ruptured by the growing prothallus, and a second rupture takes place at the base of the prothallus. The prothallus itself does not occupy the entire cavity of the spore, but after five weeks after sowing, the large-edged prothallus is developed in the lower part of the cavity (Fig. 253 d)). This is called "the endosperm," since it is similar to the endosperm of flowering plants. Goebel, however, has termed it "secondary prothallus," as the homology with the endosperm is doubtful. + +The **fertile** cotyledon divides into an upper (hypobasal) and a lower (epibasal) cell; from the latter alone the embryo is developed with its root, stem, foot, and two coleoptiles, and the former gives rise to an organ which appears in this instance for the first time, namely, a shoot with two leaves (Fig. 253 e)). This forces the embryo down into the "endosperm," which is entirely or partially absorbed by the embryo. In the case of the flowering-plants the embryo is developed with its longitudinal + +4 + +**Pteridophyta** + +233 + +axis in the elongation of the suspensor, but in *Selaginella* the em- +bryo is situated transversely to it. + +*Selaginella* (300-400 species), is essentially tropical, only one +species living in the North (*S. spinulosa*), but others grow in +Central and South Europe. + +Order 1. Lycopsida. These are extinct, woody Lycopods which are +found especially in the Lower and Middle Carboniferous. Vertically they are +most nearly related to Lycopodium, but the stem attained much larger propor- +tions than that of any living Lycopod, and was covered with a thick bark and had a +cambium by which it increased in thickness. It was regularly dichotomous, +and closely studied with spirally-placed leaves, which left behind them peculiar +channels on the surface of the stem. The sporangia were borne in groups averaging +much larger than any which are now produced (the male ones as much as +2 cm.'s in length). The macrosporangia were situated at the base, and the +microsporangia near the apex. + +Order 4. Sigillariaceae. These are, presumably, another group of extinct +tree-like Lycopsids (especially in the Middle Carboniferous). The name has been +derived from the fact that the leaves were arranged in two rows running +along longitudinal rows on the grooved stem. The rhizomes of these plants were +somewhat similar to those of *Selaginella*. + +Order 5. Sphenophyllaceae form an entirely extinct group. They do not +definitely belong to any of the three large classes of Vascular Cryptogams, but +is perhaps most nearly related to the Lycopsida. They were large herbaceous +plants with verticillate, wedge-shaped leaves, with nerves branching dichoto- +mously into equally strong branches. Micro- and macro-sporangia were formed in the same cone; and were situated in the axis of the leaves, as in the Lycopods. + +| | | +|---|---| +| **Pteridophyta** | 233 | +| axis in the elongation of the suspensor, but in *Selaginella* the embryo is situated transversely to it. | | +| *Selaginella* (300-400 species), is essentially tropical, only one species living in the North (*S. spinulosa*), but others grow in Central and South Europe. | | +| Order 1. Lycopsida. These are extinct, woody Lycopods which are found especially in the Lower and Middle Carboniferous. Vertically they are most nearly related to Lycopodium, but the stem attained much larger proportions than that of any living Lycopod, and was covered with a thick bark and had a cambium by which it increased in thickness. It was regularly dichotomous, and closely studied with spirally-placed leaves, which left behind them peculiar channels on the surface of the stem. The sporangia were borne in groups averaging much larger than any which are now produced (the male ones as much as 2 cm.'s in length). The macrosporangia were situated at the base, and the microsporangia near the apex. | | +| Order 4. Sigillariaceae. These are, presumably, another group of extinct tree-like Lycopsids (especially in the Middle Carboniferous). The name has been derived from the fact that the leaves were arranged in two rows running along longitudinal rows on the grooved stem. The rhizomes of these plants were somewhat similar to those of *Selaginella*. | | +| Order 5. Sphenophyllaceae form an entirely extinct group. They do not definitely belong to any of the three large classes of Vascular Cryptogams, but is perhaps most nearly related to the Lycopsida. They were large herbaceous plants with verticillate, wedge-shaped leaves, with nerves branching dichotomously into equally strong branches. Micro- and macro-sporangia were formed in the same cone; and were situated in the axis of the leaves, as in the Lycopods. | + +The Transition from the Cryptogams to the Phanerogams. + +All the plants considered in the preceding chapters are included in the term CRYPTOGAEMS; all in the following chapters under the head of PHANEROGAEMS (see page 8). Hofmiste's pioneer works (1851, Vergleichende Untersuchungen über den Kryptogamen, etc.) and his later researches published later (1860, Über die Vegetation, have closed the gap which was formerly thought to exist between these plants; so that we now, in the series: Bryophyta--Pteridophyta--Gymnospermae--Angiospermae see the expression of a single line of development from the cryptogams to the phanerogams. The forms through which this gradual development has taken place have in course of time, however, to a great extent died out, and only single links of the chain connecting the lowest to the highest still remain. + +The alternation of generations, which we found indicated in certain Thallophytes, can be proved with the greatest clearness in all the higher Cryptogams, from the Mosses upwards; it is also found in all the Phanerogams, but not to the same degree, because one of the generations is so far reduced that it has almost given up its independence. For the sake of greater clearness, we will begin with the comparison of the sporophyte, asexual (second) generation. + +The asexual (2nd) generation of the Cormophytes. +The asexual generation which follows from the further develop- +ment of the fertilized oosphere, is in the Mosses, only the sporo- +genous cell (Fig. 203), situated upon a short stem (Fig. 204), with a +spore-bearing leaf, situated upon a short stem, see p. 187); in +Ficileus, Equisetum, and Lycopodium, on the other hand, it is a +highly developed plant differentiated into stem, leaf, and true root, +and bearing a sporangium upon a long stalk. In this case our +shoot is very slight in Ficileus. The first leaves of the embryo +are very simple in form (Fig. 205), but after a certain age all the +leaves which arise are essentially alike. The fertile leaves do not + +9 + +**CYPTOGAMAE AND PHANEROGAMAE.** + +253 + +differ from the barren ones, and are found associated with them, and their formation does not limit the growth in length of the stem. It is only in a few of the true Ferns, and in the Hydro- +pteridaceae that fertile leaves differ materially from the barren ones. A division of labour, which occurs certainly in some, but not in all, of these groups, is found more prominently in the Equisetum and Lycopodium, for in these groups, with a few exceptions the fertile and barren leaves are very different. In the Equisetum, the fertile leaves are short-stemmed, which terminate the further growth of the short stems on which they are borne. In connection with this, leaves are sometimes developed which form a transition between barren to fertile leaves (fig. 10). This is also true in Lycopodium, and in these two first +appearance of a flower with perianth or floral-leaves is to be traced. + +Among the Cyptogams the highest division of labour is found in +Sedumiaea and Icotea, which have the two kinds of sporangia borne on separate leaves (fig. 11). The difference between these two (division) is, however, still more pronounced in the Phanerogamæ: the leaves which bear the microsporangia ("pollen-macs") have quite differ- +ent forms from those which bear macrosporangia ("the nucellus") in the same plant. The former are usually small and green; the latter are large and yellow; in certain instances, too, there is even a contrast between the "male plants" and the "female plants". Moreover, a division of +labour, in a much greater degree, takes place in the leaves which do not bear sporangia. In many plants it is impossible to distinguish in many plants to draw a sharp line not only between stamens and carpels, but also between four or five distinct kinds of leaves, which differ in form, structure, and corresponding functions, and which appear to be derived from one common type. Thus we find "scale- +leaves" and "foliage-leaves," both of which occur in the Cyptog- +ams, and the "floral-leaves," including the bracts and leaves of the "perianth," which latter often differ from each other in form and colour, and act as intermediaries into epistome and petal. In some- +stances also carpel-like bud structures are termed sporo- +phylls, and the shoot, at any rate of its shoot, whose leaves are modified into sporo-phylls, is terminated in its further growth by these +production, and is known as a flower. The flower which is most + +Floral-leaves (hypoplastic leaves) are here adopted as an equivalent of +the normal leaf-leaf (epipetalous), but not necessarily of foliage +or sporangia-bearing leaves. The term leaf is applied only to leaves in whose +until a flower is borne, and bract-like to leaves borne on the flower-stalk (peduncle). + +236 +CRYPTOGAMS AND PHANEROGAMS. + +completely furnished has calyx, corolla, stamens, and carpels arranged in this order. If the only sporophytes present are stamens, then it is said to be a male (sterilis) flower, and if only carpels, then a female (gynaeal) flower, and in both cases these flowers are sterile, or dichotomous. If stamens and carpels are both present in the same plant, then it is said to be a hermaphrodite plant in which the female flowers are situated on one plant, and the male flowers on another, are termed dioecious; and those in which the same plant bears the two kinds of flowers are termed monoecious. When the male and female flowers are found in the same species, the plant is said to be polygamous. + +The sporangium-bearing leaves — Sporophylls. In the Mosses the axonal generation is only represented by the sporophylls. The following statement is correct which considers the sporophyll to be an embryo-branching leaf with lateral stem and terminal leaf, then the spores are produced on the leaves in these plants. The sporangia in the Fungi are usually in groups (sorti) on the back or on the edge of the leaves. The number of sporangia in the Fungi varies greatly in the Marattiales and Gleicheniales (three to four in the latter, Fig. 215). In the Bryophyta the sporangia are situated in a small number on the under-side of child-like leaves, and in some cases singly, in the axils of the fertile leaves, which are alike and beautiful like mosses or micro-sporangia. In the Phanerogams there is a great difference between the stamens and carpels. + +Stamens. In many Gymnosperms (Conifers) there are many indications of relationship to the Ferns. The stamens are flat and broad, and have on the back many pollen-sacs (microsporangia) arranged in small groups (true sorti), which even have + + +A small illustration showing a cross-section of a sporophyll with spores. + + +Fig. 21.—Cyme of a stamen (male, single) seen from below. There are four polypods, one yet open, forming a "stamen"; three open polypods show a "carpel". The sporangia are on the back of each leaf. + + +CRYPTOGAMS AND PHANEROGAMS. +237 + +a small "placenta," similar to the one possessed by the Ferns, and open towards the inside by a longitudinal cleft (Fig. 241, compare Fig. 213). A section of the Conifer agree more closely. + +Fig. 240.--Stamens of Aesculus (quercus-ear long and pendulous). +Fig. 241.--Male flower of Taxus. + +with the Equisetaceae, in having a few (three to eight) pollen-sacs on each side of the stamens, which have shingle-like leaves (Figs. 242, 243, compare with Fig. 224 a, c, d). In the Abietes the number of sporangia is diminished to two, which are placed also on the lower side (Fig. 267) of a stamen. The number of pollen-sacs (microporangia) in the Angiosperms is nearly always four to each stamen; they are longitudinal projections which are + +Fig. 244.--A Cross section through a quadrilateral anther in different stages of development: a the anem where it bursts open ; b vascular bundle ; c anemous. B A stamen. C A cross section through a stamen showing the anem placed in pairs on each side of the central line of the stamen, two on the edge, and the other two generally on the side which is turned inwards; the pollen-sacs generally dehiscence longitudinally. + +238 + +CRYPTOGAMAE AND PHANEOLOGIAE. + +(quadrilocular anthers, Fig. 244). A few, for instance Ochrolecanum and Aculeopsis, have only two pollen-aces (bilocular anthers); and in others, such as Solanum and the Ericaceae, they open by pores; in Lauracea and Berberidaceae, by valves. The part of the stamen which bears the pollen-ace is termed the anther. Most frequently the anther is but slightly divided. + +**Carpels.** The simplest forms of carpels are found in Cycas. In this genus both the foliage and fertile leaves are pinulate, and hence present great similarity; the ovules (macrosporangia) are situated on the upper side of the leaf, and the pollen-aces (microsporangia), are placed on the edge of the fertile leaf of *Ophioglossum* (Fig. 245, compare with Fig. 209). The carpels of the other Cycadeae present greater divergence from the foliage-leaves, being peltate, for instance, in *Zamioc* and *Cronartium* (Fig. 246). The ovules + +A diagram showing a cross-section of a carpel with five ovules. +Fig. 245.—A carpel of Cycas revoluta with 5 +ovules (c.), at least 3 enclosed rad. sin. + +A diagram showing a cross-section of a carpel with three ovules. +Fig. 246.—Carpel with 5 ovules of +Cronartium rotundatum (d.). + +in the Coniferae are situated on the upper side and near the base of the ovaliferous scales, almost in the same position as the sporangia in the Lycopodine (Figs. 269, 272, 273 H), compare Figs. 290, 297. In some genera of the Coniferae (e.g., *Pinus*) they are situated at the base of a shoot (Fig. 204). In all these plants the ovules are not enclosed by the carpels, that is, they are not enclosed in chambers formed by the turning in of the walls of the carpel, and hence the name + +CRYPTOGAMS AND PHANEROGAMS. + +**Gynoecium** is given to them. In the higher Flowering-plants, the **Androecium**, the ovaries are distinctly situated on the edge, the upper surface, or base of the carpel; but the carpel closes round the ovaries which are therefore enclosed in a chamber—the *ovary*. In a few cases, for example in the Polygonaceae, an ovule is situated upon the upper surface of the carpel, as in the *Cucurbitaceae*; in other cases, as in the Primulaceae, many ovaries are apparently developed on the apex of the stem, which seems to have been specially adapted as a place for it. It is also worthy of remark that in these cases it appears that the ovules are not so well protected in these cases as they are in those where they are enclosed within the carpels. A single fully-developed carpel or a collection of carpels joined together is termed the *pellet*. The extremity of the carpel, which is specially developed to catch the pollen-grains and form a receptacle for them, is called the *stigma*. The lower edges of a carpel which bear the ovaries are termed the *central entree*. The back of the carpel forms the *dorsal side*. In this illustration (fig. 20) is shown a *Hydropteridaceae*, analogous to that employed by the Androecium—here, the sperms are in a corresponding manner enveloped in a closed leaf. + +The collection of stamens in a flower is termed the *androcium*, and all the carpels, whether individually free or united into one pistil, thus constitute a *gynoecium*. + +The **Sporangium**. The sexual generation of the **Mosses** is the sporogonium, in which the spores arise in tetrad from the mother-cells. The sporogonium in the Fucaceae take their origin either from a single cell or from two cells. In many species regarded as an older stand-point, from a group of cells (Kasugagynium), in both cases there may be distinguished in a mature sporangium three tissues, which have different significance (fig. 20): (1) an external layer of cells, which are usually composed of one layer of cells made up of cells of similar structure, so that on desiccation the wall is ruptured and the sporangium opens in a definite manner; (2) an internal group of cells, consisting of the gamonucleus and its derivatives; (3) an intermediate layer, which by division into four gives rise to the spores; (3) a layer of cells lying between the two already mentioned, which is dissolved before maturity. The intermediate cellular layer, which directly surrounds the spores, is termed the *tectum*, and is of greater importance than any other. It is worthy of note that none of these layers are formed by any special means. + +I may be here remarked that another explanation is possible, based on the study of the development (K). + +W. B. +8 + +240 +CRYPTOGAMS AND PHANEROGAMS. + +tion of the sporangium in the *Equisetum* and *Lycopodium* is in the main the same. + +In the *Phanerogams* the *Microsporangia* are termed *Pollen- +sack*. They take their origin from a large group of cells, which, in the *Araucaria*, are arranged in a series of parallel or semiparallel cells of the anther. In the developed, but not yet mature, sporangium (Gol- +saec) there are to be found : (as in the Vascular Cryptogams) (1) an internal group of mother-cells which give rise to the pollen-grains + +A diagram showing the development of an anther. A transverse section of a young anther of Dovici- cana nereifolia. The formation of the 4 pollen-sac-commences by division of the hyposperma-cells into two daughter-cells, one of which remains as a wall-cella, while the other becomes a pollen-cell. The latter divides into two daughter-cells, one of which remains as a wall-cella, while the other becomes a pollen-cell. The latter divides into two daughter-cells, one of which remains as a wall-cella, while the other becomes a pollen-cell. The latter divides into two daughter-cells, one of which remains as a wall-cella, while the other becomes a pollen-cell. +Fig. 217.—Development of an anther. A transverse section of a young anther of Dovici- cana nereifolia. The formation of the 4 pollen-sac-commences by division of the hyposperma-cells into two daughter-cells, one of which remains as a wall-cella, while the other becomes a pollen-cell. The latter divides into two daughter-cells, one of which remains as a wall-cella, while the other becomes a pollen-cell. The latter divides into two daughter-cells, one of which remains as a wall-cella, while the other becomes a pollen-cell. The latter divides into two daughter-cells, one of which remains as a wall-cella, while the other becomes a pollen-cell. + +(2) an external group of mother-cells which give rise to the wall-cellas. +(3) an external group of mother-cells which give rise to the wall-cellas. +(4) an external group of mother-cells which give rise to the wall-cellas. +(5) an external group of mother-cells which give rise to the wall-cellas. + +The first three groups are formed by division of the hyposperma-cells ; that is, in this case by division of those cells which only make part in forming the outer-wall and internal cellulo, which corres- pond to the outermost layer of cells in the *Vascular Cryptogams*. These cells are drawn with thicker walls in B-E. The commonest form of the vascular bundles is that in its simplest form, viz., that in which there is no vascular bundle at all. This is the case in the *Phanerogams* where they are active and in which tangential divisions par- ticularly occur. In this case also there is no tapetal layer. In *Equisetum* and *Lycopodium* transverse sections through an older anther, the thickness of the wall round each mother-cell is less than that round any other cell. In this case also there is no tapetal layer. In *Equisetum* and *Lycopodium* transverse sections through an older anther, the thickness of the wall round each mother-cell is less than that round any other cell. In this case also there is no tapetal layer. + +In *Equisetum* (fig. 218), (1) a group of cells surrounding these, of which the internal ones form a tapetal +layer, similar to that in the Vascular Cryptogams ; the tapetum, +(micropore), in this case also formed in tetrad ; (2) a group +of cells surrounding these, of which the internal ones form a tapetal +layer, similar to that in the Vascular Cryptogams ; the tapetum, + +6 + +CHYTOGAMAE AND PHANEROGAMAE. +241 + +and some of the cells surrounding it in this group, become dissolved before maturity; the more external ones, on the other hand, are provided with peculiar thickenings, and form the "fibrous" layer by the aid of which the deliquescence of the stamen takes place; (3) an internal layer, the epidermis, enclosing all the other layers (Fig. 247). + +In some Coniferae (Cupressus, Thuja, and several species of Juniperus) the microsporangia (pollen-sac), which are situated on the under side of the stamen, are covered with a thin cuticle, which is perforated by numerous pores, and which is supposed to be homologous with the indusium of the Ferns. + +The Ovule in the Phanerogamæ arises most frequently on a projecting portion of the carpel, termed the placenta. The ovules (compare the sporangium of the Euphorbiaceae and especially the pollen-sac) take their origin from a group of cells which lie beneath the epidermis (Fig. 248 A, B). First of all a small papilla is formed, which is later on provided with a vascular bundle and becomes the funiculus; this probably has the same value as the vegetative axis in the ferns. At first only two funiculi are attached. Only one macrosporangium (exocline ; Fig. 248 no.) is developed at the apex of the funiculus. This arises by a process of cell-division exactly corresponding to that by which the pollen- + +A: A small papilla +B: A vascular bundle +C: A group of cells +D: An ovule +E: An exocline +F: A funiculus +G: A macrosporangium +H: A placenta +I: An ovary +J: A carpel +K: A cuticle +L: A pore +M: A cuticle +N: A placenta +O: A funiculus +P: A macrosporangium +Q: A placenta +R: A cuticle +S: A pore +T: A placenta +U: A funiculus +V: A macrosporangium +W: A placenta +X: A cuticle +Y: A pore +Z: A placenta +AA: A funiculus +BB: A macrosporangium +CC: A placenta +DD: A cuticle +EE: A pore +FF: A placenta +GG: A funiculus +HH: A macrosporangium +II: An ovule +JJ: An ovary +KK: A cuticle +LL: A pore +MM: An ovary +NN: An ovary +OO: An ovary +PP: An ovary +QQ: An ovary +RR: An ovary +SS: An ovary +TT: An ovary +UU: An ovary +VV: An ovary +WW: An ovary +XX: An ovary +YY: An ovary +ZZ: An ovary + +Fig. 248.—Development of the ovule in the Red Currant, Ribes rubrum, arranged obliquely to show the different parts. The upper part shows (1) a group of cells (inner integument); (2) outer integuments; (3) mesophyll; (4) parenchyma (middle-cord of the embryo-sac). + + +Firstly, a small papilla is formed, which is later on provided with a vascular bundle and becomes the funiculus; this probably has the same value as the vegetative axis in the ferns. At first only two funiculi are attached. Only one macrosporangium (exocline ; Fig. 248 no.) is developed at the apex of the funiculus. This arises by a process of cell-division exactly corresponding to that by which the pollen- + +242 +CRYPTOGAMS AND PHANEROGAMAE. + +sacs are formed (Fig. 243 C-E), with this difference only, that while a great many cells may be distinguished in each pollen- +sac, which forms pollen-grains by tetrad-division, only a few are found in the ovule, and all these moreover are suppressed, with one +single exception which develops into the macrospore (Fig. 243, +y) within the embryo-sac, the latter being a true egg. The wall of +the embryo-sac, in the Gymnosperms, may be thick and divided into +two layers and partly cuticularized, as in the spores of the Cycy- +ogamæ (Fig. 243 D). In the Angiosperms, on the other +hand, the wall is extremely thin. +The pollen-sac thus stands in the same relation to the nucellus +as the microsporangium does to the macronangium; in the +pollen-sac and in the nucellus, two sporules are made by +tetrad-division from several mother-cells; in the nucellus and micro- +sporangium, a reduction of the cells already formed takes place to +such an extent that the number of macrospores becomes one +(Schizogamy) or two (Polygamy) or four (Sporogamy), or rarely a +large number as in *Imites*. + +In the Ferae, as stated on page 210, etc., *doladaria* covering the +sori very often occur. Hercestris and Club-Mosses have no +indusium; but in all Phanerogamæ except one-like structures +(organogamæ) are found which envelop the sporangia when they de- +velop from the upper end of the funicle (Fig. 243 y and z; in Fig. 240) +and enclose the nucellus on all sides as a +sac, leaving only a +small opening at the apex of the nucellus—the *micropyle*— +(Fig. 240) through which the pollen- +tube proceeds to the +embryo-sac. The +ovules of the Gym- +nosperms are formed only by +the integuments +(Figs. 251, 254, 269, +271) and the same +are two integuments (Fig. 242). +In shape the integuments resemble very closely the cupular + + +A diagram showing various forms of ovules. The labels are: k - karyon; l - lumen; m - micropyle; n - nucellus; o - outer layer; p - pollen tube; q - pollen grain; r - radicle; s - sac; t - testa. + + +Fig. 243.—Various forms of ovules. A an even ovule (orthotropous); B reversed (antitropous); C curved (neptropous); D cupular (cycloid); E inverted (inverted); F an even ovule with a large testa (hemicarpal); G an even ovule with a small testa (hemianthous); H an inverted ovule with a large testa (hemicarpal); I an inverted ovule with a small testa (hemianthous). The labels are: k - karyon; l - lumen; m - micropyle; n - nucellus; o - outer layer; p - pollen tube; q - pollen grain; r - radicle; s - sac; t - testa. + + +**CRYPTOGAMAE AND PHANEROGAMAE.** 243 + +Indusium of the Hymenophytae, certain Cyatinaeae (Fig. 81D) and Sabulina (Fig. 215); that they are really homologous with those is proved by the fact that the majority of the authorities regard them as structures found only in the Phanerogamae. + +The ovule is thus a " monogam" (i.e. reduced to 1 aporangium, the anecaulia) normal, situated on a funicle, and enclosed by one or two capsules (orthotropes), or integuments (complectomes). The majority regarded (anatropae) (Fig. 240). + +[Goebel (1884 and earlier) with Strasburger considered the entire ovule of the Phanerogamae as homologous with the macrosporangium, the integuments how- ever as vestigial remains of the sporangium. This view is not cor- respond to the stilk of the spongonium. The integuments of the ovule (according to Goebel, 1887) differ from the inclusion of the Funiculi in plants being devel- oped from the same egg-cell, and are therefore not homologous with the anatropae and Isoclea, a portion (outgrowth) of the leaf which bears the epinyma (A).] + +The nucellus is the only macrosporangium which never opens; the macrospore remains enclosed in its, and the macrosporangium remains attached to it. The method of fertilization in this case differs from that of the Cryptogamae; the method of fertilization which is employed should be very different from that of the Cryptogamae. The pollen-grains must be transferred to the ovule, and retained either by a drop of mucus at the micro- pyle (Hymenophytae), or by means of a special organ (Angiospermae). Fertilisation by sperms, spermatids, which are known to freely motile has been discovered in the Cycadeae and in Ginkgo. + +Many other modifications, unknown in plants of more simple structure, have been observed in these plants; such as: in the fertile leaves; especially: in the form of the stem or cladodes (hypo- gynous, perigynous, epigynous); in the development of the peri- ach which stands in intimate connection with the special means employed; in the union between the different grades of union found in the leaves; in the union of the flowers into aggregations of a higher order (inflorescence), and at the same time the production of " floral-leaves" (page 255). + +**The sexual generation. The Fertilisation.** + +The sexual generation in the Mosses is relatively well developed, because not only the protonema, but all the other vegetative parts of the Moss-plant, in addition to the archegonia and anthero- diah, belong to it. In the groups which follow, a gradual but increas- ing reduction of the sexual generation takes place, and at the + +244 + +CRYPTOGANES AND PHANEROGAMAE. + +same time an indication of sex is found in the prothallium, which finds expression in the forms of the sporophytes. In the majority of cases, the prothallium is green, leafy expansion which can sustain itself by the assimilation of carbonic acid, and by the absorption of nutrient from the soil by means of root-hairs. In some plants (Ophioglossum), the prothallium is brownish-yellow, in a tubular pale, tubular body, but in these instances it is relatively large. In the heterosporous Vascular Cryptogams and in the Phanerogamae, the prothallium is much more reduced, both as regards its size, and also with respect to the number and structure of its cells and vacuoles. + +1. The Microspores. Amongst the Hydropteridales the con- +tent of the microspore divide into three cells, from the lower one of which a small lenticular cell is cut off, while from the two upper ones a simple archeithidium is developed. The male prothallium is thus reduced in this group to a very few cells. In the heterosporous Lycopo- +diaceae also, the prothallium is represented by one small lenticular cell, and by two or three cells, from which arise two or three +in Sedges (Fig. 253) to a large number of spermatones (Fig. 253), but in Isoetes to only four. The spermatones are set free through rupture of the microspore-wall, by the swelling of the wall of the archeithidium, or by the breaking up of the latter. The liberated from the sporangium (Soralea), the upper cell of the prothallium elongates and perforates the walls of both the microspore and the sporangium (Fig. 214) in order to ordinate the archeithidium, thus resembling the prothallium of some Lycopsidae. + +In the Poaceae, the microspores are termed pollen-grains. + +In the Gymnospermae, the male prothallium is represented by a small cell cut off internally by a curved wall from the large pollen- +cell (Figs. 250, 257), the primitive cell of which is large. The large cell, by division, gives rise to two or three great nuclei, each called mainly as vegetative nucleus (Fig. 250) into which the vegetative nucleus passes. The small cell, corresponding to the rudiment of the archeithidium, divides into 1, 2 or 3 small cells, the innermost, +whence arises a stalk-cell or pollen-tube, and an outer sterile cell. +This divides, either after cutting off an inner stalk-cell or directly, into two generative cells, which in Cycadeaceae and Gink- +goaceae are liberated from the pollen-tube as spermatones, or, +as in the higher Gymnospermae, pass into its anterior end as spored + +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. +A diagram showing a microspore dividing into three cells. + +CRYPTOGAMS AND PHANEROGAMES. +245 + +cell without cells. After the rupture of the membrane at the tip of the pollen-cube they penetrate into the archegonium, reach the oosphere and complete the fertilisation, the sperm-nucleus fusing with the nucleus of the oosphere. + +In the anisogamous the reduction pro- +cesses differ little. The pollen-grain contains two cells, a vegetative cell and an antheridal cell, but these are not, as in the last group, separated by a true cell-wall; the membrane at most being formed between them. The pollen-tube grows through the oosphere, but the vegetative cell disappears about the time the pollen-tube reaches the oocyte; while the antheridal cell divides into two cells, one of which fuses with the nucleus of the oosphere, the other uniting with the definitive nucleus. + +The Gymnosperms prove that this is not a general rule, for they are more closely related to the Cryptogams than are the Angiosperms. When the pollen-grain begins to germinate the external wall ripens as in the Crys- +tophales (Fig. 286), and in some cases special germ-pores are formed in the cell-wall for the emergence of the pollen-tube. + +2. The Macroglossae. The prethallium in *Salvinia* and *Marisella* is still rather large, green, and capable of the independent assimilat- +ing life. In *Salvinia* there are three archegonia and +beams (in *Marisella* only one) in each archegonium, which however are embedded to a greater degree in the prothallium, and are more reduced than the archegonia of the true Ferns and Horse- +tails (*Nephrolepis*). In *Salvinia* there is no sex-difference in *Indice* and *Seduminae*, partly because it is smaller and is in a higher degree enclosed in the spore; it also contains less chlorophyll, or is entirely without chlorophyll, and in consequence incapable of independent assimilation; partly because it is very small; and +partly because the archegonia are themselves reduced, the cells of +the neck are fewer and embedded to the level of the surface +of the prothallium without any, or with only a very slight +projection (Fig. 287). In *Seduminae* there is no sex-difference, +archegonia begin to develop in *Seduminae* while the macrospore is still within its sporangium, and before it is set free from the mother- + +246 + +CRYPTOGAMAE AND PHANEROGAMAE. + +plant. After the spores are set free and germination has com- +menced, the sporophyll ruptures and the perthallium is exposed. +The **oxygoni** germinate and form internally a cellular tissue, designated in former times by the name of **albina** (endosperm), which is homo- +logous to the **endosperm** of the seed plants. The **endosperm** is de- +embryonar, and is a parenchymatous mass containing a large supply of nourishment. In the upper part of the endosperm a number of +A diagram showing the structure of an embryo. +**anogonia** are developed which are in the main constructed in +A diagram showing the structure of an embryo. + +Fig. 251.—Longitudinal sec- +tion of an embryo of *Ceratopteris*. +(1) The neck, consisting of 3 +cells. Inside the integument +(2) the **endosperm**, consisting +of 3 cells. In the center of +the **endosperm** is seen +an oval cell, which is the +**endosperm** itself, and at its top two +parenchymatous cells are +formed in each way thus this +structure consists of 5 cells, +but nearly 3 terms down, +two are seen to be united. +In the same manner as those in the Cryptogamae, but are still more reduced, the neck consisting only of 4, 2 or 1 cell (Figs. 251, 252). +The ventral canal-cell is also formed, in the majority, as a small portion detached from the neck; the larger remaining portion becomes the oosphere. When the pollen-tube has passed down to the oosphere (Fig. 253) and fer- +tilisation has been effected, the coenospore commences a cell-formation, +the final result of which is the formation of three layers, one, termed +the suspensor, and the embryo is forced more or less into the endo- +251 + +Fig. 252.—The apex of the oosphere (or of an ovule of +*Obera*). Longitudinal cells which guide the pollen-tube, +and a small oval cell which forms the nucleus of the **endosperm**, +is a recent canal-cell, and +the other two cells are those of +the Cryptogamae should be compared with those pages 181, + +252 + +CRYPTOGAMAE AND PHANEROGAMAE. +247 + +sperm in which it may rest for a longer or shorter time, and generally is destroyed to such an extent that it has a distinct primary-root (radicle) and stem (plumule) with one or more embryo-leaves (cotyledons). + +When the copulae have been fertilised its nucleus sinks down to its lower end, and by repeated division into two, forms four cells lying in one plane (Fig. 233), but held together by a thin membrane, which is the first inter-vernier division of these four. It is in the intermediate one of these which elongates and forms the suspensor, or four suspensors, if they separate from each other, which are attached to the base of the embryo. It is from these four lower cells that the embryo (or four suspensors) that the suspen- +A diagram showing the structure of a seedling. +
Fig. 234.—Embryo-sac of Conium purpureum synangium. The upper part shows the central nucleus, and the suspended suspensor.Fig. 235.—The apex of the mesocarp (cyst) of Allium in longitudinal section. The embryo-formation has commenced at the bottom of the hollow cavity, and is seen to be a bud of the macrospore (pollen-grain) + pollen-cortex.
+ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
**MONOCOTYLEDONES.**
*Juncus (Rush) has glabrous foliage-leaves, generally cylindrical, rarely flat; the edges of the leaf-shafts are free ("open" leaf-shafts) and cover one another. The capsule, 1- or 3-locular, with many seeds.* --*Luzula* (Wood-Rush) has flat, grass-like leaves with entire edges; the edges of the leaf-shafts are united ("closed" leaf-shaft). *Carex* (Sedge) is similar to *Luzula*. *Prionium*; *S. Africana*; resembling a *Tecoma*.
The interior wall of stamens, in some species, disappears partially or entirely; in others, it remains.
Some of the numerous Juncus-species (e.g. *J. effusus*, *placens*, *concolorum*, etc.), have false lateral inflorescences, the axis of the inflorescence being pushed into one side of the plant, and the flowers being arranged on this side only. This condition of the stem, and resembles it both in external and internal structure.
The foliage-leaves of the genus were formerly described as "undulate-stem," because their edges are undulate.
In the following species, however, the stem was said to be "leathery"; i.e., *cf. ephusa*, *placens*, *concolorum*. Sterile paraphyllumous cells are found in the pith of these stems and in the leaves.
Other genera belonging to this order are: *Eriophorum* (Cotton-grass), *J. balticus* (Tundra rush), *nuphar*, and others.
The inflorescences most often present are those which are composed of several branches, each bearing several fertile and sterile axes.
Their composition is as follows:---The flowers have either no bractlets, and the inflorescence are then capitulate; or they have 1- several bractlets.
Each branch bears 1-2 fertile axes, and 1-2 sterile axes ("intermediate-axes"), and succeeding this are generally several bracteae borne alternately and in the same plane as the branch;
the uppermost (the "false-leaves") being always larger than the lower ones.
The sterile axes are usually called "bractlets," and are termed "intermediate-axes."
If no bractlets occur in the axis of the branch-leaves,
then the succeeding branches are always borne on the posterior side of the first branch.
In this case,
there is only one fertile intermediate-leaf,
then the lateral axes are always on the upper side,
and a "false" lateral inflorescence occurs;
if there are 2 fertile intermediate-axes,
then there is a "false" lateral inflorescence;
if there are three,
being several,
then a "moss," or spike.
+ + +
JuncaceaeDescription
Some of the numerous Juncus-species (e.g. *J. effusus*, *placens*, *concolorum*, etc.), have false lateral inflorescences, the axis of the inflorescence being pushed into one side of the plant, and the flowers being arranged on this side only.
This condition of the stem,
and resembles it both in external and internal structure.
The foliage-leaves of the genus were formerly described as "undulate-stem," because their edges are undulate.
In the following species,
however,
the stem was said to be "leathery"; i.e., *cf. ephusa*, *placens*, *concolorum*. Sterile paraphyllumous cells are found in the pith of these stems and in the leaves.
Other genera belonging to this order are: *Eriophorum* (Cotton-grass), *J. balticus* (Tundra rush), *nuphar*, and others.
The inflorescences most often present
are those which are composed of several branches,
each bearing several fertile and sterile axes.
Their composition is as follows:
The flowers have either no bractlets,
and the inflorescence are then capitulate;
or they have 1- several bractlets.
Each branch bears
1-2 fertile axes,
and
1-2 sterile axes ("intermediate-axes"),
succeeding this
are generally several bracteae
borne alternately
and in
the same plane as
the branch;
the uppermost (the "false-leaves") being always larger than
the lower ones.
The sterile axes
are usually called "bractlets,"
and are termed "intermediate-axes."
If no bractlets occur in
the axis of
the branch-leaves,
then
+ + +
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+ + + + +426 + +427 + +428 + +429 + +430 + +431 + +432 + +433 + +434 + +435 + +436 + +437 + +438 + +439 + +440 + +441 + +442 + +443 + +444 + +445 + +446 + +447 + +448 + +449 + +450 + +451 + +452 + +453 + +454 + +455 + +456 + +457 + +458 + +459 + +460 + +461 + +462 + +463 +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +A diagram showing a flower cluster with three main stems and several smaller stems branching out from them. +Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., syn., Tillea affinis (L.) Schrad., +Tillea affinis (L.) Schrad., +Tillea affinis (L.) +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +Tillea affinis +TILLEA AFFINIS + +The leaves are simple, entire, ovate-lanceolate to oblong-lanceolate, +with acuminate apexes. +The petiole has no stipules. +The leaves are opposite. +The leaves are alternate. +The leaves are whorled. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. +The leaves are imbricate. + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * * + +* * * * +* The genus Malvastrum Mallowes). The plants are easily recogniz- ed by their scaly stem-scales, simple persistent, most frequently lobed, stipulate le-aves folded in bud ; but perfect, regular, +hypogynous flowers, with gamopetalous, persistent, 5-merous calyx + +**Genus Malvastrum Mallowes)** + +**Malvastrum** Mallowes). The plants are easily recognized by their scaly stem-scales, simple persistent, most frequently lobed, stipulate leav- es folded in bud ; but perfect, regular, +hypogynous flowers, with gamopetalous, persistent, 5-merous calyx + +426 +**DICYOTYLEDONES.** + +with coateate maturation; the 5 petals twisted in the bud and united with one another at the base, and by the 5 apparently numerous stamens (Figs. 445, 448), with the filaments united into a tube, with uniform bilobular anthers opening by a crevicular slit (in 2 valves). Carpel: the ovary usually 3-locular, but sometimes 2-locular, and the cotyledons are folded (Figs. 447, 451); endosperm scanty, often mucilaginous. Most of the plants belonging to this order are herbs, often clad in pubescent or with delicate hairs. The leaves are most frequent on palatable or on poisonous plants. + +An epizyseis is often formed by *fused-leaves* placed close beneath the calyx, in some 3, in others several. The median leaf is posterior in the species which have only one style, and anterior in those which have two. The petals are twisted either to the right or to the left in accordance with the spiral of the calyx; they are most frequently oblique, as in the other plants with twisted cotyledons, and are rarely erect as in *Ceratophyllum*. The corolla droops as a whole, united with the staminal tube. Only the 5 petal-stamens are present; they are generally very numerous (see Fig. 446; the sepals-stemme is completely suppressed); these 5 staminial leaves are then united into a tube, frequently 5-falcate at the top, and bearing the + +Fig. 445.-Longitudinal section through the flower of *Althea* silvestris. +Fig. 446.--Diagram of dites stemme. +anther on its external side. The pollen-grains are specially large, globular and yellowish-white. It is about half of the carpus mulberry-like and placed round the summit of the axis which most frequently projects between them. There is only 1 style, which is generally divided into as many stigma-bearing branches as there are stamens. The fruit is a capsule or a berry-carpel or capsule. Endosperm (Figs. 447 & 451) scanty, often mucilaginous round the calyx, which is rich in oil. + +The order is closely related to that of *Ceratophyllum*, which appears especially near to the *Bryophyllum*, but is separated from these and from the *Tillaea*, among other characters, by its b-lobular (subordinarily c-lobular) anther. + +The sub-orders may be arranged as follows:--- + +A diagram showing a diagram of dites stemme. + +COLUMNIFERA. +427 + +I. Carpels in one whorl. + +A. The fruit a capsule, most frequently with loculicidal dehiscence, and many seeds in each loculus. + +r. Gossypium. The staminal-codium is naked at the apex, blunted, or 5-dentate.--Gossypium (the Cotton plant) has an epicalyx of five sepals, which are often persistent, and a persistent calyx. Solitary flowers. Large, most frequently yellow, corollas. A 3-5-valved capsule with many spherical seeds. " Cotton " is the sea-hairs developed upon the entire surface of the seeds (Fig. 447), but in some species they are confined to the base (and therefore white); these are thin-walled, with a large lumen, and during drying twist spirally, and come together more or less in the form of hands. They consist of cellulose, and have a cuticle. +---Zizyphus has several, most frequently narrow, glandular-leaves, a distinct 5-lobed or 5-partite calyx.--Abutilon; *Melod*. + +A +Figs. 447.--A Seed of Gossypium with hairs; B the same in longitudinal section. + +2. BORAGINACEAE. The staminal tube is more or less deeply cleft into bundles, sometimes with a central column; the style is long and slender; the stigma, if any, is short and terminal. Almost all plants belonging to this group are trees, and in many instances have large barrel-shaped stems that is, swollen in the centre, and somewhat constricted towards the base; the leaves are usually simple and alternate. The flowers are often enormously large, and have beautiful petals; in some they unfold before the leaves. The capsule-wall is sometimes closely covered on its inner surface by minute hairs; in others it is smooth and glabrous gener- +ally without hairs. These hairs, however, on account of their brittle nature, cannot be used like those of the Cruciferae. Digitate leaves are found in the *Frankenia*, *Baccharis*, *Limonium*, *Ceratostigma*, *Oenothera*, short stem, and in the American *Silk-cotton tree* (*Bombax*, *Kradendron*, *Chloris*). Olethrix is a genus of trees belonging to this group. Durio is noted for its delicious fruits, which have a most unpleasant smell. +(*Bombax malabaricum* is dioecious; the five equal-stamens repeatedly*) + +428 + +DIOTYLEDONES. + +branch, and the filaments bear unilocular anthers; the five petal-stamens bear bilocular anthers.) + +B. Schizocarps, with 1-seeded fruitlets, most frequently nut-like and reniform (Figs. 400, 451). + +3. MALVAE, MALLOW. Genus. The carpels are arranged in one whorl (Fig. 400), and the stamens are 5 ; the stamens are 1-2-lobed ; the stamens equal that of the carpel ; fruitlets 1-seeded, reniform, indehiscent, but detach- +ing themselves from one another and from the persistent central column (Figs. 400, 451).—Malvae has an epigynous of 3 free leaves. +A flower of Malvae is a monadelphous flower, with 5 sepals, 5 large leaves; of these support a homodromous foliage-shoot which forms a repetition of the main axis, the other an antifoliumous flower which continues the branching of the main axis. The genus Malvae, like Maltese, has an epigynous of 6-7 leaves united at the base. Lactuca, Lotus, Lotus, Lotus, Bistaria, etc., have no epigynus. + +400. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +401. + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +3 + +COLUMNEIFER. + +other even before maturity : there is, however, only 1 style, divided into a corresponding number of branches (this condition may be considered to have arisen from the branching (shoot-forming) of 3 carpels). Mucuna has 8 large, horizontal (diastolicic 3-foil) epipetalous leaves, united at the base. Ptelea has no epicalyx. + +**Foliation.** The majority have profusely branched flowers, and are pollinated by insects. The flowers of the species of *Mucuna* are protected from the rain by hairs, e.g. in *Mucuna silvestre*. When the flower first opens the numerous anthers occupy the centre of the flower, and the still unopened anthers are protected by a sheath-like structure. When the anthers are withered and empty, and the stigma protrudes and assumes their place, the sheath-like structure disappears. In *Mucuna* this is accomplished only by insects ; but self-pollination takes place in small developed flowers, e.g. *Mucuna retusa*, in which the stylar-branches, twisting themselves, place the stigma in between the undeveloped anthers. + +A diagram showing the structure of a flower in Mucuna silvestre. + +**DISTRIBUTION.** 800 species (of genera), most of which are natives of the Tropics, especially America. *Aethes* and some of the species of *Meloe* are native of Europe. *Gomphrena* is found in North America. *Gomphrena* is tropical, we doubt especially Asiatic (*G. hirsutum* from India, &c., *orlorense* from Upper Egypt). Cotton was introduced into California about 1850, and it is now very abundant there owing to the arrival of the Europeans. + +**Uses.** Fungicid and poisonous properties are certainly wanting ; mastice, on the other hand, is abundant in all parts of the plant. Medicinal: the root of *Aethes officinale*, leaves and flowers of *Meloe*-species (*M. silvestre*) + +430 + +DIOTYTLEDONIEX. + +**valpurtis and brevica** (and **Gyropinus**).—The seeds contain a large quantity of fatty oil, which in some cases extracted (Cotton-seeds and others). The seed-hairs of the Cotton plant are the most important product of the culture. The cultivated forms of the genus are distinguished by their long, narrow leaves, which are opposite, or alternate, or both, according to the species. The common cottons (Naxalim), brevica, and others. According to other botanists, there are only 5 species. Both is obtained from *B. b. Hirculus communis* (Banboo-hemp, Africa). + +**Hirculus communis** (Linn.) is a very valuable plant, and is used in tropical countries as a vegetable; but they are not so productive as the *Cotton*. The flowers are yellowish-white, and are used for making wines, and honey; and honey is extensively cultivated in certain parts of Europe.—Ethnol. sect. and ascendent flowers (see next page).—The flowers of this species are very beautiful (Hirculus albastrusca, and others).—Many are cultivated as ornamental plants on account of the large flowers, e.g., Hookholy (L. rosea, etc.), Latraria eremica, Melogia grandiflora and infida, Melon spicata, Hirculus ranae albastrum, apriana; *Sphacelium*. + +Family 14. Tricocceae. + +The very large or small Euphorbiaceae and three smaller ones belong to this family. They have in common: unisexual, hypogynous, frequently regular flowers, the perianth most frequently single, rarely double, or entirely wanting; so that there is such a great variety in its structure and form as to show that it has been once cited among the plants of the same genus composed of 3 carpels forming a 3-lobed ovary, which is frequently more or less deeply grooved (hence the name, Tricocce); in the inner angles of the loculi are found 1 or 2 (sometimes) pendulous (except *Euphorbia* sp.) stamens with an upper appendage or spur; frequently swollen, microphyll (Fig. 453). The seed most frequently has a large endosperm and a straight embryo (Fig. 453 B, 464).—The female flowers are called *Pistillaria* and *Chasembore*, it may perhaps be regarded as an offshoot from the Sterculiaceae. + +Order 1. Euphorbiaceae. Flowers unisexual. In each of the loculi of the ovary, generally 3, there are 1 or 2 pendulous ovaules with upward and outwardly turned microphyll. The placenta is protodioecious (Fig. 454, 465).—The capsule is usually opening at the top of the capsule; the carpels are often spirally twisted; frequently with great violence, ejecting the seeds and leaving a central column. Endosperm copious.—For the rest, the flowers present all stages, from green to naked with only a cordel; of which there are the most reduced in Nature, namely the naked, lamellated flowers of *Raphanus*. + +The same variety which is found in the flower is also present in + +TRICOCHEMIS. 431 + +the vegetative parts. Some are herbs, as our Spurgeas, others are shrubs and trees; some African Euphorbia-species even resemble the habit of a Cactus. Leaf-like branches with rudimentary leaves are found in *Phyllostachys* (sub-genus *Xylopia*) (Fig. 456). The leaves of the *Cynara* are compound; they are nearly always simple. Large, highly-branched cells contain a great quantity of pungent latex are found in many, and watery juice in others. Glands and glandular hairs are general—Only a few genera have spines. + +As an example of the most perfect flowers (which partly reproduce the Gennaricous type) may be mentioned, *Croton*, *Manihot*, and *Zatophy* ; 5 sepals, 5 petals, sometimes gamopetala- +na, androecium diaphanous, or many-stamened, often mono- +diphaneous. + +A small illustration showing a flower structure. +**Fig. 453. — A-flower (incomplete).** + +**Fig. 454. — B-flower in longitudinal section.** + +**Fig. 455. — A-sepal and cotyle. B-in longitudinal section.** + +Ricinum (Castor-oil) (Figs. 453-455) : monocotyledon ; the 5 -flowers, situated in the lower portion of the inflorescence, have 5 perianth- +leaves ; the stamens 2-3 ; the pistillate flower has 3-5 perianth-leaves ; 3 bifid styles. Leaves petiolate, palmately lobed. The seeds (Fig. 455) contains an abundance of fatty oil and large albumen graina.—*Mercurialis* (Mercury); the perianth is usually free from the stamens ; the stamens are inserted on the y-flowers most frequently a 2-locular gynoecium.—*Phyllostachys* : *Pride* &c., A3, united in some and forming a column in the centre of the flower (Figs. 457, 458) ; *Xylopia* is a section of this genus— + +w. n. +47 + +432 + +**DIOTYLEDONES** + +*Hura crepidina* (Sand-box tree) has a many-carpellate gynoeceum, which separates with great violence when ripe.——A drupe is found in *Hippeastoma semicirculare* (the Mancilin-tree, W. L.),—*Alchermora* (Cleopatra's) illicium, a plant of the genus "puncturea,"—*genus* *genae*, the ?-plant has been introduced into England, but nevertheless produces seeds capable of germination; these have generally several embryos. + +*Euphorbia* (Spurge) has the most reduced flowers, which are borne in a very complicated inflorescence. Each 2-flower (Fig. 460 B) is naked, and consists of one stamen only (here-missing), and two sepals; the closely allied genus *Anthosoma*, a small perianth is situated at the place where, in *Euphorbia*, there is a flower (Fig. 461 A). The 2-flowers (Fig. 460) are naked, with a 5-lobular ovary and 3 hillocks; the perianth is a distinct perianth (Fig. 461 B); in a few *Euphorbias* traces of a perianth are present. In *Eu-phorbia*, the flowers are grouped into flower-like inflorescences termed "cyathia." + +Each cyathium consists of a central phallic 2-flower which is first of all surrounded by 5 groups of 2-flowers (stamens) placed in a zig-zag, with a terminal phallic 2-flower (Fig. 459 B), that these flowers are surrounded by a series of leaves united into a leaf-shaped structure (Fig. 450, 1–5); on its edge are placed 4, generally crescent-like, yellow glands, one in each of the intervals, except one, between the lobes of the involucre (shaded in Fig. 459; see also Fig. 460 A). Smile-like + +Fig. 450.—Florifera (Xyloglypha) acutifolia. +Fig. 451.—Leaf-like branch with flowers (cat. iii6). Fig. 457.—2-flower; and Fig. 458.—Cyathium. + +THESCOCLE. +433 + +thin structures (floral-leaves?) are situated between the 3-flowers. The 3-flower has a long stalk, and finally bends down on one side, namely to the place on the edge of the involucre where the gland is not developed. These cataphia are again arranged in an inflorescence which commences as a 3-5-moded umbellate cyme (phleoclinum), the branches of which ramify dichotomously and finally as + +A diagram of an inflorescence (cataphium) of Euphorbia with 3 floral-leaves, e., a supporting caker epicalyx, b., a perianth, c., a corolla, d., a calyx, m., n., l., 3. 4. 5. floral-leaves in their order of appearance); the shaded portions are the connate glands. +Fig. 403.—Euphorbia Integra. A an (umbel) inflorescence (cataphium). B the cyme after the removal of the involucre. + +A diagram of an inflorescence (cataphium) of Euphorbia with 3 floral-leaves, e., a supporting caker epicalyx, b., a perianth, c., a corolla, d., a calyx, m., n., l., 3. 4. 5. floral-leaves in their order of appearance); the shaded portions are the connate glands. +Fig. 403.—Diagram of an inflorescence (cataphium) of Euphorbia with 3 floral-leaves, e., a supporting caker epicalyx, b., a perianth, c., a corolla, d., a calyx, m., n., l., 3. 4. 5. floral-leaves in their order of appearance); the shaded portions are the connate glands. + +A diagram of an inflorescence (cataphium) of Euphorbia with 3 floral-leaves, e., a supporting caker epicalyx, b., a perianth, c., a corolla, d., a calyx, m., n., l., 3. 4. 5. floral-leaves in their order of appearance); the shaded portions are the connate glands. +Fig. 404.—Different : e., (a) and f.; (b) flowers; g., the petal ; h., or the tube; i, the ovary. + +205 genera; more than 8,000 species; especially in the Tropeo-phyllum are used on account of the oil, and of the pungent (aperient, poisonous, antiliminitic, + +1 + +434 + +DICOTYLEDONES. + +etn.) prospicuous in the inner or the seeds. **Official:** "Cacaliis-bach" of *Garden cistus* (the falty oil of the seeds of Crotan triphyllus (Trop. Asia)); "Can- +for oil" from *Eucalyptus camaldulensis* (Australia, and cultivated in all warm climates throughout the world), and "Cacaliis-olive" from *Cacalia olivifolia* (Europe). **Etymology:** this also yields a red dye. Gum "Euphorbium" is the hardwood (resinous) latex of the Crotan-like *Euphorbia hirta* (Morocco). --Nuttall's plant: Member of the family Euphorbiaceae. The gum is used in medicine, and some +rota form a very important article of food in the Tropics (Cassava-flower, +Tapioca or Brazilian arrow-root). The fresh latex of the root in some species is a powerful emetic, and is employed in medicine, as well as in cooking. Cacaliis is obtained from *Cacalia elatior* (Trop. S. Am.). The vegetable gum is extracted by boiling with water, and its large quantities in such factories. An indigo-like dye is obtained from *Cacalia* +tinctura, and is also found in *Mercurialis perennis*. Bleaching is obtained from *Streptocarpus pygmaeus*. Ornamental plants: *Dendrophora*, *Croton, Dutchman's-pipe.* +--Hippomane is poisonous. + +Order 2. Buxaceae. This order differs from the Euphorbiaceae in having the outer layer of the seed-coat (testa) composed of two layers, viz., the +stamens; the 2 lower a 6-parted perianth and 3 capsules. Capsule with +hemicidal dehiscence, the inner layer being detached externally from the outer. +--30 species. --The genus *Buxus* (Box) is an ornamental shrub (poisonous); it has a very hard and valuable wood which is used for wood engraving and carving. + +Fig. 405.--2-flower. +Fig. 405.--2-flower. + +**Fig. 406.--Longitudinal section of the ripe fruit.** + +**Fig. 407.--2-flower.** + +Order 3. Calycanthaceae. Aquatic plants, growing at the bottom of shallow +waters, with opposite leaves, and bearing a single flower on a stalk, which are +generally crowded and form a rosette in the axils of the leaves. The flowers are +unisexual (monoeccious), i.e., either male or female, but both sexes may be +present, and are provided with two delicate bractlets; when only one sex occurs, +of only 1 terminal stamen (Fig. 408), the 2 flowers of a biaperturate gynoecium +(2 cotyledons) are united into a single ovary, which is surrounded by a calyx +in the case of the genunum of the Labiate, by the formation of a false partition- +wall; in each locule there is 1 pendulous ovule with a membranous turned +cotyledon. Fruit: 2 aperturate achene (Fig. 408). --Spurge--Calycanthus. + +Order 4. Euphorbiaceae. Euphorbia: E. rigida (Greenberry). + +Fig. 408.--Calycanthus stipulatus. +Fig. 409.--Longitudinal section of the ripe fruit. +Fig. 410.--2-flower. + +TEREBINTHINE. 435 + +is a heather-like, moorland, evergreen under-shrub with linear leaves, having a deep groove closed with hairs, on the under side. The erect cyme shows the flowers in two rows, the upper one being larger than the lower. The calyx is 3-4-leaved, 8-10-flowered, 8-staminate; in the $y$-flower, 6-8-lobular ovary. Fruit a stone. + +Family 15. Terebinthine. + +The diagram of the flower (Figs. 465-467) is the same as in the Granales, namely S., P., A2 and G in which of 5 (less frequently 3, 4, 6, 5), and the same modifications also occur with the suppression of the petal-stalks. The flowers are sometimes cap-like (capitulum) and the cyme (corymb) is found between the androecium and the gynoecium (Figs. 465, 466). The flowers similarly are regular, hypogynous, $\frac{3}{2}$ and polyadelphous, though exceptions are found to all these characters. For example, united sepals and petals free from each other are found in some species, while in others there is suppression of one sex. In most cases the flowers are small, greenish-yellow, and arranged in paniculate inflorescences. The corolla (most frequently $y$) are few in a few, but frequently united into a multilocular tube, usually with 1 or 2 lobes at each mouth. The gynoecium in the Anacardiaceae is so reduced that it has only 1 fertile loculus with 1 ovule. The cymes are epigynous, i.e. ana- +treponous with outward-turned rachis (except the Anacardiaceae). + +The flowers are often solitary or in cymes (panicles), often compound (pinnate) leaves without stipules, and as in addition they frequently contain aromatic, especially terpenoidal-like substances, they assume a certain resemblance to the Walnut trees, and were formerly included in this family. The fruit is a nut. The species of genera of the volatile, scented oils are found in special glades in the bark of the branches and in the leaves, in the latter case appearing as *pelicoid* dots. This family includes several orders which are derived from plants growing from calcareous soil. + +Order 15. Conaraceae. This order forms the linking link between Terebinthine and Boleteae (Volvaceae) as well as Leguminosae, with which they are sometimes related. The flowers have 5-merous whorls; 2 ovules in each biseriate loculus; stamens equal to or exceeding the number of follicles; seed with aril. Shrubs with scattered (most frequently pinnate) leaves, without stipules. 170 species. Tropical. + +The flowers are usually solitary or clustered, often pinnate leaves without pellucid dots and exstipules; the sepals are nearly always entire. +The corolla is usually regular; the calyx is either 3-4-lobed or 2 whorls of stamens: 3-4 carpels in the gynoecium. A very characteristic feature is the union of the filaments into a tube, on the edge of which stipula-like teeth are often found. There are most frequently 2 ovaries in the loculi; + +A diagram of a flower from Terebinthine family. + +456 +DICOTYLEDONES. + +fruit a capsule with many winged seeds in *Swietenia* (Managogy tree ; Trop. Am.), *Cedrela*, etc.; berries in others. The wood of *Cedrela* is used for making chairs and other articles. + +Order 3. Rutaceae. Leaves glandular with pellucid dots. +The type is the same as that of the family. Flowers 4–5-merous. +The ovary is most frequently 4–5-grooved. Disc well pronounced, +often appearing as a "gymopore". The majority are shrubs with alternate or opposite leaves, but some are herbaceous. + +A. The ovary is deeply 2-cleft with basal styles which are more or less united; the carpels in some genera are entirely free (groups 1, 2). +The fruit is cupular and most frequently dehisces like foliaceous along the ventral suture or septically, so that a horn-like internal layer (endocarp) separates adaxially from the external layer. + +1. Zanthoxylum. Zanthoxylus; Chilgoza; Escalera. +2. Bumexus. Australia—Coralwood. +3. Drimys. South America—Drimyse; Africa—Drimys; Colotemera, Euphorbiaceae, and *Bumexus*. Officialia: *Bumexus* coriaceae and *botanica*, "broad Burma leaves" (E. serratifolia and Euphorbia arborescens, "mango Burmese leaves"). + + +Description of flower. + + +Fig. 407.—Fruit. Lateral section of flower. +Fig. 408.—Ruta. Floral diagram. + +4. RUTA. Ruta (Figs. 405–407) gracilis is an herbaceous, glaucous, strongly smelling plant with bipinnate leaves and yellow flowers; the terminal flower is 5-merous, the others 4-merous (S. Bur.).—Dictionary: symmorphic flower. The individual carpels + +TEERENTHINE. 437 + +of the fruit separate from each other, and dehisces like follicles, upon which the internal layer is detached elastically and spring out, carrying the seeds with it. +Several species are ornamental plants. + +5. *Cephalanthus*—Flowers in cymes; calyx often ovoid-moriform with gamopetalous corolla ; stamens 5.—Tecoma; Galium (G. officinale); S. Am.; "Cortex an- +guiculata"; Caprifolia; Althaea. + +6. The ovary is entire or only slightly grooved; the style is terminal, undivided. The fruit is most frequently a drupe or berry. + +6. Tomatellum. *Fruit* : winged fruit. The bolls are enclosed in the leaf- +sheaths. *Siliquaria* : Pholidendron. + +A flower with five petals. +403 + +A cross-section of a fruit showing the internal structure. +403 + +Fig. 403.—Branch with compound leaves. +Fig. 403.—Transverse section of fruit. +Fig. 403.—The fruit is enclosed in the leaf-sheath. + +7. *Aurantia*, Orange Bunch. Fruit a berry with a leathery external layer.—The most typical flower is found for example in +*Lemonia*: S5, P5, A5 + 5, G5 (2-5).—Citrus has 4-5-8-merous + +438 +DICTYOTLEDONES. + +flowers, a gamosepalous, dentate only; free petals, one whorl of stamens which are split irregularly into several bundles (Fig. 470). The fruit is a multifloral berry provided with a thick, tough, outer layer. The juicy pulp, which fills up the loculi and envelopes the seeds, is very hard and fibrous, and contains numerous structures, which arise on the inner side of the wall at the loculi and by degrees entirely fill them up; the disseminations remain thin, and form the partitions so easily separating from each other (Fig. 469). The seeds are numerous, and are contained in several embryos. + +The blade of the leaf is separated from the frequently winged stalk by a node (and hence is a compound leaf with only the terminal leaflet developed) (Fig. 468); in other genera, as in *Ceratophyllum*, it is developed trilobate leaf. Thorns are frequently developed. The species of this genus is native of the warmer parts of S. E. Asia, are very hard to separate. The differences between them are chiefly in the number of leaves, thorns, and in the number of stamens. Citron officinales, *Citrus* (Indica); *Citrus* citriodora, *Citrus* limon (Indica); *Citrus* aurantiifolia, *Citrus* aurantium (Indica). + +INTRODUCED INTO INDIA IN THE 18TH CENTURY. + +The orange (introduced into India in the 18th century), *Citrus* aurantiifolia (Fig. 469), Blite Orange (introduced into Europe at the time of the Crusades); the nurple (Hirten Orange) *Citrus* aurantiifolia var. aurantifolia (Fig. 470), is a native of India; it is cultivated in many countries for its fruit; this species especially that the essence of Neroli is made. C. aurantiifolia, C. bergamia, C. limon, C. reticulata, C. aurantiifolia var. aurantifolia, C. limon var. citroides, C. limon var. aurantiifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. aurantifolia var. +Order 4. +Bumaceae. +Fruit a drupe; 1-2 stones; The bark, as well as the other parts, are aromatic; the leaves are alternate; the flowers are hermaphrodite; the fruits are edible; they are used medicinally; they are found in tropical regions; they are found in some parts of the globe and E India. + +The incense of Bactria is medicinal (Frankincense). + +The resin (Essence) of Prosthemia officinalis is official and is used exclusively for medicinal purposes; it is also used as a perfume (N.S.M.). + +Prosthemia officinalis: *Amargi* (1 carap.), 270 species; tropical. + +Order 5. +Zygophyllaceae. +The majority have opposite, pinnate leaves with stipules; the flowers are hermaphrodite; they are found in tropical regions; they are found in some parts of the globe and E India. + +The most important in Dioscoreaceae (West India), the wood (Lignum Vitae) of which is very hard and heavy, this wood and Gum gumacaruba are official medicines; they are found in tropical regions; they are found in some parts of the globe and E India. + +Laurus nobilis: *Laurus* nobilis (Indica); *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* nobilis: *Laurus* + +INTRODUCED INTO INDIA IN THE 18TH CENTURY. + +The incense of Bactria is medicinal (Frankincense). + +The resin (Essence) of Prosthemia officinalis is official and is used exclusively for medicinal purposes; it is also used as a perfume (N.S.M.). + +Prosthemia officinalis: *Amargi* (1 carap.), 270 species; tropical. + +Order 5. +Zygophyllaceae. +The majority have opposite, pinnate leaves with stipules; the flowers are hermaphrodite; they are found in tropical regions; they are found in some parts of the globe and E India. + +The most important in Dioscoreaceae (West India), the wood (Lignum Vitae) of which is very hard and heavy, this wood and Gum gumacaruba are official medicines; they are found in tropical regions; they are found in some parts of the globe and E India. + +1 + +**Aesculinae.** 439 + +*exocle* yields *Jamaica Quassia*; the bark of *Simaruba*, *Simarouba-secopera* and others in use. *Simaruba-secopera* is a garden plant (imparting leaves, winged fruits) used in Jamaica. + +Order 7. **Ochnaceae.** Flowers dioecious, 5-merous. The unilocular ovary, which is individually free, project considerably into the air around the ground, and is usually pendulous. The calyx is 5-parted, the sepals alternate, with stipules. Order 8. **Oxerae.** —160 species; tropical; especially American. + +Order 9. **Corylaceae.** The ovary rarely contains more than 1 ovule, even though there be several loculi and several carpels; in *Aesculus* all the 160 examples except one become suppressed. Branches—*Aesculus*. The perianth is a single whorl of 5 sepals, which are often persistent on the body about the form and size of a pear (cf. *Accolideus* from Tron, Am. and A. *Cathcartii* on *) but in the latter the kidney-shaped nut (the so-called "Cathcartii") on *) is very large. *Morus* (from *Morus*) (from R., E.) is cultivated in several tropical countries on account of its delicious fruit, which is eaten raw or cooked in various ways. The leaves are oval. +Several species of *Bassia* are ornamental shrubs in this country, for instance, in *Iris pseudacris* (N.Am.), *Rutina* (the fig-wire), the leaves flower-stalks of the same plant being used to make a kind of tobacco pipe (cf. *Rutina* from N.Am.) is poisonous. Chinese gall is produced by the sting of a leaf-horse (*Chrysops chrysops*) on *R. succisifolia* (China), and Japanese wax is from the tree *Jasminum sambac* (Japan). The flowers of *Corylus avellana* (Europe) are used in tanning and as a black dye. *Ornithogalum*: the musaic resin of *Pancratium luteum* (the Musaic-tree, from the Mediterranean). The fruits of *Fragaria vesca* (the strawberry) are used in making preserves and jam. +450 species; tropical. + +Order 9. **Aesculinae.** Flowers 4-merous; karyomorphous: eocarpic ovary or ovules surrounding the gynostemium; in the (daisy-like) loculi of the ovary, 2 anomalous ovules—390 species; tropical. + +Family 16. **Aesculinae.** + +The essential characters of this family are in the main the same as those of the Terebinthineae and Graminaceae. The flowers are hypogynous, perfect, with free petals, 5-merous (Ss, Pp), typically A5–5, all of which, however, are not generally developed; in our native plants they are represented by a few species only (usually a 3-merous, 3-carpelous gymnosperm (see frequently 2 or 3 carpels with as many locally). In each loculus there are usually only 1–2 ovules. A deviation from the preceding families is the frequent occurrence of an epigynous ovary with an epicalyx or a zone of symmetry (Fig. 471). When a disc is developed it is placed outside the stamens. The majority have no endosperm (Fig. 473). +—the members of this family are nearly all trees. + +The family is closely allied to the Terebinthineae, but unlike this it never has + +440 +DICOCTYLEDONES. + +aromatic properties, and differ also in the position of the nectary, in the flowers, which are often irregular with a reduction in the number of stamens, and by the presence of a perianth (the perianth being reduced to a tube or cup) (the Terebithinae having the pericarpule turned upwards), etc. It is also related to Frangulaia, the Stipuleaeae being the chief connecting link; but the Sarcinales are more closely allied to the Rosaceae. + +Order 1. Staphyleaceae. Leaves opposite, often compound. Flowers regular, with 5 sepals, 5 petals, and 5 stamens. The perianth is usually included in the nectary. Ovary generally 3-lobular, opening at the apex, and has several very thin veins. The flowers are mostly small, and are found in the Mediterranean region. The species of *Pistacia* (Europe) and *Rutaceae* (N. Am.) are cultivated in gardens; they have whole flowers in pendulous, axillary racemes or panicles—16 species—Stipuleaeae. + +Order 2. Melanthiaceae. Glaucescent shrubs with sessile leaves, pinnate leaves, and large stipules. + +Order 3. Sapindaceae. Trees or shrubs, often climbing by tendrils (lannes with anomalous structure of the stem) and with compound leaves. The flowers, in most cases, are small, insignifi- +471 +472 +473 + +Fig. 471.—Diagram of the flower and of a scopic organ. +Fig. 472.—Flower in longitudinal section. +Fig. 473.—Seed in longitudinal section. + +rant, and without seeds; or in some bionomical genera and synmorphic. Stamens AB are free from each other (inside the nectary (dio)); ovary generally 3-lobular, with 1-2 ovaries in each loculus (raphe ventral, micropyle turned downwards). Seed without endosperm, often with an aril. The embryo is often thick and curved (cf. *Caryophyllus*). + +*Eucrasus* (House-Christmat). Trees with opposite, deciduous, dem- +tate leaves without stipules; the inflorescence is composed of unpaired scrophoid gymnes arranged in a pyramidal panicle (termed a thyrsus). The flowers are irregular, with an oblique plane of + +A diagram showing the structure of a flower and a scopic organ. + +441 + +**ASCULUM.** + +geometry (through the 4th sepal, Fig. 471): there are 5 sepals, 5 free petals, of which the one lying between S¹ and S² is the smallest (see Fig. 471) and may be absent ; stamens 7 (3+4), three being suppurated : gynostemium simple, 3-carpellary and 5-lobular, with single or two free stamens (Fig. 472). The fruit is a 3-valvate, sometimes spiny, capsule, with biconciculate dehiscence, the seed having a large hilum, a curved embryo without endosperm, and cotyledons (the radicle) free from the testa, Fig. 473). *Jatropha curcas* (Greece, Asia), introduced into cultivation about 300 years ago; the majority of the other species, e.g., *E. parie*, etc., several of which are frequently cultivated in gardens, are from N. America. + +The flowers are hermaphrodite, but in some species the authors of style when visiting the flowers. The flowers are protogynous. + +The fruits are capsules, or berries, or drupes, or nuts (sepalid capsule, nuts with or without wings, achizocarp), etc. Sor- +jasus, Carpinus serratae, Scuticaria, Krocotricha, etc. (about 118 genera, 670 species); *Caryophyllus* (about 10 genera), *Pachystoma* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 genera), *Pachysandra* (about 2 generations) and other species, from Asia. + +Order 4. **Aceraceae.** This order is so closely allied to the Sapindaceae that some authorities have classed it with them. +The main difference lies in the regularity of the flowers, and the **2-nervi- +ous gynostemium** (in all +occurrences of carpels occur)—they +are trees, and, like the +Horse-Chestnuts, have opposite leaves and stipules; in Acer the leaves are palmisored, +but imparipinnate in +Nyssa; both are fre- +quently cultivated in +gardens. The flowers are often regular; gynostemium comes species have **3**, **5**, and +**6**-flowers; sepals, petals free, stamens **8** (that is, **5+3**, but +the two median ones are absent) inside a large disc. Fruit a +samara (achizocarp) with **2** winged, nut-like fruticlets (Fig. 474). + +Fig. 471—Seeds of Acer platanoides. + +442 +DICOTYLEDONAE. + +In each of the 2 locali of the ovary are 2 ovaries. Embryo curved, with thin, folded cotyledons. Endosperm absent. The inconspicuous sex organs are represented by a few stamens (the number sometimes has 10 stamina), when the lateral branches are developed they are similar to the main axis. In some species both corolla and petal-stems are represented by a single leaf-like structure. The flowers are found in North Temperate zones. Acer is the Tertiary in the Oligocene. The following are native plants: Maple (Acer campestre). Sycamore (L. platanoides), ash, birch, elm, oak, maple, linden, poplar, willow, sugar cane obtained from the young sap of the Sugar Maple (N. Am.). + +Order 5. Majesticae. A tropical (especially American) order closely related to the Magnoliales, but differing in having the leaf at the base of the petiole. Some species are leaves with conspicuous stem-structure. Leaves opposite. The flowers are regular, with 5 sepals and petals, and a plane of symmetry passing through the middle of the flower. Important characteristics for this group are the numerous glandular struc- +tures on the surface of the petals and sepals, and the presence of nectar glands in the calyx and corolla. Examples: Bocconia, Bauhinia, Calophyllum, Tetrapanax, Hemerocallis, etc.—About 600 species. + +Order 6. Erythrophytae. Sepals 3, petals 5 (with a ligular corona), 10 stamens (sometimes reduced to 8 or 6), and a pistil with a single ovule (especially American) trees and shrubs, the Cean plant (Erythrina cuprea) being best known. Its leaves are considered by the inhabitants of Chili and Peru to be a remedy for all kinds of diseases; they possess intoxicating, exhilarating properties, and contain the alkaloid cocaine, which is frequently employed as a local anesthetic—180 species; chiefly in America. + +Order 7. Yuccaceae. Trees; Topm. A. 1stanum—140 species. +Order 8. Trigoniaceae. Shrubs; Topm.—8 species. +Order 9. Tremandraceae. Polyglosses with regular flowers—27 species. +Australia. + +Order 10. Polypalacae. Herbs or shrubs (some tropical species are lianas) with scattered (nearly opposite), simple and most frequently quite extensive compound leaves; often with a terminal spike or raceme, and are strongly zygomorphic (the plane of symmetry being median); their flowers are regular, with 5 sepals and petals, one of which (4 and 5 in Figs. 475, 470) are very large, petaloid, and frequently project on each side like the "wings" of a Persephone; another, b., of which the two halves only are visible in the perianth (noted on Fig. 475), and the "heel" (Fig. 470 c) is large, hollow and boat-shaped, and frequently + +Fam. 35.—Order of Polypalacae. +Pistil a. A single ovule in each of the two sides of the flower; a. and b. the two calyces bracteoles. + +A diagram showing a flower with five sepals and petals. + +FRANGULINE. +443 + +with a lobed or dimarated edge (Fig. 476 A and B); stipules &c, +the two median ones being absent, all united into a tube split +along the back, which is also slightly united to the keel (the +authors, often 2 localia, open by pore, Fig. 476 E, a); the 2 median +carpels form a biconical ovary. A petiolate ovule in each loculus +(Fig. 476 D, a) with a large basal placenta, but without lateral dehis- +cence; rarely a nut. Polypodea (Milk-wort). + +470 species; distributed over the whole globe (see Article. OFFICIAL: the root of F. sanguina, from N. Am. Some are used as ornamental plants. + +The leaves are simple, entire, or pinnately divided, usually finely beaded. +The dimarated flowers of the anterior petal support this insertant when it alights. +The anthers lie on each side of the stigma in the pouch of the anterior petal; +the upper one is free, the lower one is attached to the upper one by a small revol +stigmatic lobe. In reaching the honey the proboscis of the insect must come +in contact with the pollen and the viscid stigma, by which it is rendered sticky; +this causes the pollen adhering to the proboscis and so being carried to other +flowers. + + +A - A leaf with stipules. +B - A flower with petals and stamens. +C - A flower with petals and stamens. +D - A flower with petals and stamens. +E - A flower with petals and stamens. +F - A flower with petals and stamens. +G - A flower with petals and stamens. +H - A flower with petals and stamens. +I - A flower with petals and stamens. +J - A flower with petals and stamens. +K - A flower with petals and stamens. +L - A flower with petals and stamens. +M - A flower with petals and stamens. +N - A flower with petals and stamens. +O - A flower with petals and stamens. +P - A flower with petals and stamens. +Q - A flower with petals and stamens. +R - A flower with petals and stamens. +S - A flower with petals and stamens. +T - A flower with petals and stamens. +U - A flower with petals and stamens. +V - A flower with petals and stamens. +W - A flower with petals and stamens. +X - A flower with petals and stamens. +Y - A flower with petals and stamens. +Z - A flower with petals and stamens. +AA - A flower with petals and stamens. +AB - A flower with petals and stamens. +AC - A flower with petals and stamens. +AD - A flower with petals and stamens. +AE - A flower with petals and stamens. +AF - A flower with petals and stamens. +AG - A flower with petals and stamens. +AH - A flower with petals and stamens. +AI - A flower with petals and stamens. +AJ - A flower with petals and stamens. +AK - A flower with petals and stamens. +AL - A flower with petals and stamens. +AM - A flower with petals and stamens. +AN - A flower with petals and stamens. +AO - A flower with petals and stamens. +AP - A flower with petals and stamens. +AQ - A flower with petals and stamens. +AR - A flower with petals and stamens. +AS - A flower with petals and stamens. +AT - A flower with petals and stamens. +AU - A flower with petals and stamens. +AV - A flower with petals and stamens. +AW - A flower with petals and stamens. +AX - A flower with petals and stamens. +AY - A flower with petals and stamens. +AZ - A flower with petals and stamens. +BA - A flower with petals and stamens. +BB - A flower with petals and stamens. +BC - A flower with petals and stamens. +BD - A flower with petals and stamens. +BE - A flower with petals and stamens. +BF - A flower with petals and stamens. +BG - A flower with petals and stamens. +BH - A flower with petals and stamens. +BI - A flower with petals and stamens. +BJ - A flower with petals and stamens. +BK - A flower with petals and stamens. +BL - A flower with petals and stamens. +BM - A flower with petals and stamens. +BN - A flower with petals and stamens. +BO - A flower with petals and stamens. +BP - A flower with petals and stamens. +BQ - A flower with petals and stamens. +BR - A flower with petals and stamens. +BS - A flower with petals and stamens. +BT - A flower with petals and stamens. +BU - A flower with petals and stamens. +BV - A flower with petals and stamens. +BW - A flower with petals and stamens. +BX - A flower with petals and stamens. +BY - A flower with petals and stamens. +BZ - A flower with petals and stamens.) + + +Family 17. Franguline. + +The plants belonging to this family, with very few exceptions, +are trees or shrubs. The leaves are usually simple; stipules may be absent or present. The flowers in almost all the orders are symmetrical; they are regular or irregular; they have 5-6 sepals, +2-5 carpels, but never have more than 1 whorl of stamina, which in *Elaeagnaceae* are placed opposite the petals (typically 5+5 or 4+4 stamina, of which however either the ex- +ternal or internal pair may be wanting), or perigynous or +slightly perigynous, in *Elaeagnaceae* only strongly perigynous or epigynous; generally 2 ; the calyx is inconspicuous; petals free or + +444 +SILKYTYLEDONIES. + +slightly united. Gynoeceum simple; corolla generally multilobular; +style short or entirely wanting. A disc is normally always developed +in the flower, but is found sometimes inside the staminal whorl, +sometimes outside it or between the stamens. The ovules are +apertous (antheropons with dorsal or ventral raphe). + +Order 1. Celastrales (Celastraceae). The name (tree-like) may +be chosen as a type. It is a shrub with simple, opposite leaves +and small caducous stipules. The small, greenish-yellow flowers, +borne in regular alternation, are regular, 5-6, with 4 whorls, +4-5 (or 3) per whorl in regular alternation, the calyx being small, +upon which the petaloid corolla (imbriicate in the bud) and +the stamens are borne, with a slightly perigynous insertion. The +style is short and erect; the ovary is erect ovulate in each +locule. The fruit is a 4-carpel 4-septate capsule, which usually +dehiscesse; the seeds are few in number, and have a large, red- +yellow aril (developed from the micropyle). Embryo green, in a +large, fleshy, white endosperm. + +The dingy yellow flowers are generally +visible only when they are taken by the wind; they do not +grow on long stalks, and they do not open until the day after +nightfall. The stigma and style remain till several days after the +fruit ripens. The leaves are deciduous, and fall in autumn. +Order 2. Celastrus, Cassia, etc. + +Order 3. Aquifoliaceae (Hollies). The genus Ilex forms +almost the entire order. (170 species out of ISO; especially from +S. Am.) They are shrubs or trees with scantly pubescent or glabrous leaves (in Ilex aquifolium, spinny) +with very small stipules. The flowers are small, white, and borne +in the axils of the foliage-leaves; they are most frequently bisexual and dioecious. +The calyx is persistent; the stamens and carpels in regular al- +ternation; the calyx and corolla have their leaves slightly connate; + +Fig. 47.—Ilex aquifolium ; magnified flower. + +4 + +FRANGULINE. +445 + +stamens slightly adnate to the corolla; the ovary is generally almost spherical with a thick, sessile stigma (Fig. 477). This order deviates especially from Celastraceae in the absence of the dios and in having only 1 (Cendrelas) ovule in each of the 4 loculi of the ovary, and in having usually 4 stamens. The anthers are small, at the apex of the large filaments with the radicle directed upwards—3—genus.—L. equitum (Holl.) principally on the coasts of European countries; from Norway to W. Denmark, and further southwards to S. France, and S. Germany, and also in S. Russia. Several South American species contain so much caffeine that they may be used as a beverage in the place of tea (L. paraguariensis, Paraguayensis, Paraguayensis, or Maté). + +Order 4. Ampelidaceae (Vines). Shrubs with the stem swollen at the insertion of the petioles and climbing by tendrils borne opposite the leaves (Figs. 478, 479). The leaves are scattered (generally 1), stalked, stipulate, frequently palmented and lobed, and often with a petiole. The flowers are solitary or occasionally borne in paniculate corymbose, whose position is the same as that of the tendrils (Fig. 478); they are hypogynous or slightly hypogynous, $q$, with 4—sepalas, petals, and stamens (which, as in the Rhododendrons, are often absent) (Fig. 480, A, B). The calyx is very small, entire, or slightly dentate; corolla valvate, and in some falling off as a hood, since the individual parts remain united at the summit (Fig. 480 A). Between the laminae and groove of the calyx is a long disc-like structure resembling the stamens (Fig. 480 A, B, E). In each loculus of the 2-lobeular ovary there are 2 erect ovules ($B$); the style is short or wanting. The fruit is a berry. The embryo is small and lies in a hypanthium sometimes slightly folded (reniformis) exocarpus (Fig. 480 C, D). + +Filix and Ampelis (Eucalyptus flowers): Clava (4-memous flower): Leon (without stipules, corolla gamopetalous). The inflorescence in Pieridaceae (Fig. 481) consists of a single flower on an axis, on the edge of which $q$ flowers are borne, and on the surface $Y$ flowers. + +The tendrils in Ampelidaceae are modified branches, since they bear leaves and stipules like those of other plants; but their origin is not really the inflorescence as borne in the position of the tendril; and tendrils are met with which are partly infertileous. The explanation of the position of the tendril is that it has been developed from a leaf-stalk which has been much reduced. The relative positions are as follows: in Filix virensa the following two kinds of shoots and relative leaves produce one flower (the other being omitted): a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with a leaf-leaflet; a leaf-stalk with + +446 + +DICOTYLEDONES. + +opposite the lowest 8-5 foliag-leaves no tendrils are found, then follow: 2 foliag-leaves with tendrils, 1 without a tendril, 3 with and 1 without, etc., with great regularity. Buds are developed in the axils of the foliag-leaves. + + +A branch with bunch of grapes. + + +Fig. 479.—Branch of the position of leaf and tendrils. The branch is divided into sections or nodes (a) and internodes (b). The leaves are opposite to each other, green, white and shaded ; 1 buds. + +Fig. 480.—Diagram of a branch off the corolla ; B flower after the removal of the corolla ; C, D longitudinal and transverse section of seed ; E longitudinal section of gymnosperm * euryale.* + +Fig. 481.—Diagram of branch and position of leaves, at tendril ; at the main axis ; at axil of leaf ; at base of leaf ; at base of leaf ; at first two foliag-leaves with their stipules ; long-bush in the axil of a (everything appearing in this branch is entirely black) ; u, the first leaf of this branch. +435 + + +Diagram showing the structure of a plant. + + + +Diagram showing the structure of a plant. + + + +Diagram showing the structure of a plant. + + + +Diagram showing the structure of a plant. + + + +Diagram showing the structure of a plant. + + + +Diagram showing the structure of a plant. + + + +Diagram showing the structure of a plant. + + + +Diagram showing the structure of a plant. + + + +Diagram showing the structure of a plant. + + +FLEXULEACEAE. +447 + +(Fig. 479): these develop into two narrow-branches, which commence with a internally-placed small branch (Fig. 481) succeeded by several foliag-leaves with a divergence of $3\overline{6}$ in plane at eight angles to that of the mother-branch, but the whole shoot is extremely small, and the first branch (Fig. 481, $a$) in its axil remains. This bud in its following year develops into a new shoot, which again produces a second branch (Fig. 481, $b$), and so on. In the dwarf-branched, their plane coincides with that of the long branch from which it is developed (the grandiose axis). The tendency does not doubt may most seriously be opposed to this theory, because the buds of the dwarf-branch are always lateral. + +The branches are thus symmetrical, whose successive shoots bear al- +ternantly 1 and 2 foliag-leaves; thus, on the figures there are portions analogous to those of the fig-tree (Fig. 480), and also to those of the fig-plant (Fig. 482). + +The following facts however are adverse to this theory: (1) the first leaf on an auxiliary bud is then situated $1\overline{6}$ from the subdormant-leaf (e.g. the foremost leaf of the first shoot); (2) the second leaf is situated $1\overline{6}$ from the first (Fig. 482); (3) the Distylis-plant is that in which placed only about $50\overline{6}$ on one side. (2) The buds of the dwarf-branch are placed alternately and sister-buds to the symmetrical shoots, but their first shoots have a different relative position to this, which is very peculiar, and still more remarkable for the fact that they are all placed in such a manner that no two leaves coincide ; thus we only find accessory buds in the cases where no tendrils are opposite to the leaves, and the main bud must then be considered to be suppressed, (Fig. 483). It is therefore evident that the buds of the dwarf-branch grow-pointing of the stem or by division, and do not develop, as might be expected, from the apex of the shoot. But these relations, however, find their explanation in another way than that given above. For instance, both modes of operation are opposed to them. + +All species of Flexulea and Trupiae; they are rare in America. In N. Am. some Fissile-species and Ampelodesmum quinquedentum are found. Vitis vinifera is supposed to have originated in the distinct East and South of the Continent; but it has been shown by Mr. Hooker that it was introduced from Asia Minor, and "raisin" (the name "carnet", given to a species variety with small, seed- +less fruits, is derived from Corinth.) The species of Ampelodesmum (Virginian Grape-vine) are found in America. + +Order 5. Rhamnaceae. The stamens are placed opposite the petals as in the Ampelodesmum (Fig. 482), but the flowers are much more perigynous or entirely epigynous. The trees and shrubs belonging to this order are mostly evergreen or semi-evergreen woody plants; they frequently thorny (modified branches). The flowers are inconspicuous, sometimes unisexual (Fig. 482), and have 5 (-4) sepals, petals, stamens, and generally 3 (-5) carpels. The calyx has little or no stimulation; the petals are very small (except in some species); they often appear as hollows embracing the stamens; a disc covers the inner surface of the thalamus or the base of the style in the epigynous flower; gynoecium simple, + +W. H. +G8 + +448 +DICOTYLEDONES. + +with one style and one erect ovule in each loculus. The fruit is most frequently a drupe. The embryo is large, often green or yellow, with endosperm. + +*Buxus sempervirens* (Buckthorn) has a juicy drupe with 3 (3-5) stones, surrounded by a fleshy layer by the persistent portion of the receptacle; the disc is the *E. californica* (common Buckthorn); dioecious, with opposite, serrate leaves. *R. frangula* (Alder Buckthorn); flowers 3, with scattered, entire leaves—*Cunonia* (S. Am., with richly developed endosperm), *Cotoneaster* (Europe, Asia, S. America), *Euphorbia*, *Physalis*, *Pomaderris* (Austr., fruit a capsule). *Zizyphus*, *Ficus*, *Colletia* (S. Am.) are thorny shrubs; *C. pinnata* has thorny shoots with small, reflexed leaves; *C. spinosa* has long, pendulous foliage-leaves. *Oberea claudia* has tendrils as in the *Amplidium*, e.g. *Graecum*. + +A diagram showing the structure of a flower. +40 + +Fig. 40.—Buxus sempervirens: A, long-styled 2-flowered; pet sepals; B short-styled 2-flowered; pet sepals. +41 + +475 species, 40 genera; chiefly in temperate and tropical climates. Some are medicinal plants, the bark and fruit having purgative properties (the bark of *Buxus sempervirens* and *Cassia Sagra*) from the bark of *J. pinnatus* are official). The fruits of the following are edible: *Zizyphus lotus*, Z. vulgaris, Z. opus Christi, etc. Green and yellow dyes are obtained from the fruit of *R. cathartica*, *leptocera* and others (Avignon grain). *Cunonia*, *Buxus* and evergreen Physalidaceae are ornamental shrubs. + +Family 18. Thymelaeaceae. + +Exclusively trees or shrubs with simple, entire, scattered leaves without stipules. They have a strongly perigynous, regular, 4-merous flower with a corolla of 4 petals and a calyx of 4 sepals; the gynoecium formed of 2 ovaries and with, in many cases, 1 ovule, bearing on its edge 4 (or 5) petaloid sepals and, but rarely at the same time, small scale-like petals. The corolla is most frequently entirely white or yellowish-white (rarely red or purple among the Monochlamydeae); frequently only one of the 2 whorls of stamens, which are situated on the inner side of the edge of the receptacle, is developed. The fruit is most frequently a 1-seeded + +A diagram showing the structure of a flower. +42 + +THYMELAEACEA. 449 + +berry or drupe, or a nut which may be falsely berry-like, the partly persistent receptacle being flabby and enveloping it. + +This family appears the most nearly allied to the Frangulaceae, especially the Rhinanthaceae, and may be considered as a further development of those in the direction of the Corolla-Flowers. The corolla is wanting in the majority of the corolla and gymnoecium, which in this instance only consists of one carpel. Another deviation is that both the whorls of stamens are present, while one of them is wanting in the Frangulaceae. They also appear to be related to the Lamaceae (see page 305). + +Order 1. Thymelaeaceæ. The flowers are most frequently 5 (Fig. 483). The receptacle is high, generally tubular, coloured, and bears on its axis the 4-(or 5)-merous calyx, with imbricating involucral leaves, and the 5-merous corolla, often with small scales. The stamens are situated on the inside of the receptacle, and number 4+4 (or 5+5); stigma capitate. 1 *pendulous* corule + +Fig. 683.—Daphne mezereum; A flower; B longitudinal section of pistil. + +(Fig. 483 F), the radicle pointing upwards. The fruit is most frequently a berry; a seed is sometimes developed. Indehiscent, wanting or very slight. + +Daphne (Sparge-laurel) Fig. 483 has a deciduous receptacle, often coloured; sepals 4; petals absent; stamens 4+4. Berry,—Giraudia (Giraudia); *Ferndale* (2 stamens); *Phytolacca* and *Pascuana* and *corolla*. + +400 species; chiefly in the warm, sub-tropical zone, especially the Cape and Australia. Only Daphne and Phytolacca in Europe. In the fruit and bark of some forage plants (e.g., *Cynara*, *Cynara*, *Cynara*) there is a bitter juice. The bark of *D. mezereum* (native and cultivated) and *D. insitiva* is official. A specifically tough bast is obtained from *Daphne cneorum*. *Laurus nobilis* (Bay laurel) is used in waxing. Some are cultivated in gardens as ornamental shrubs, especially species of Daphne. + +Order 2. Elaeagnaceæ. Shrubs or trees, which are easily recognised by the covering of pilose hairs found upon almost all + +450 + +**EOTYLTLDONEX** + +parts of the plant, causing them to assume a silvery or rusty-brown appearance. +Stipules are absent; the leaves are simple, most fre- +quently scattered. Flowers (Figs. 484, 485) frequently unisexual. +The sepals are 3-6, the petals 3-6, the stamens 3-6 or 4+5 or +0+4. The ovule is erect and the radicle turned downwards (Fig. 486). +The fruit is a nut, but becomes a false fruit, being surrounded by the persistent receptacle or the lower part of it, and thus assuming a berry-like appearance. The flowers are usually very conspicuous and signi- +ficient. —Shepherdia (opposite leaves) has 4 sepals, 4+4 stamens, +as in Daphne. —Dioecious.—Elaeagnus (Silver-leaf) is ?, has 4-6 +sepals, and 4-6 stamens alternating with them. —Hippophaë is +dioecious, but has only one flower on each branch (the ?-flower perhaps properly speaking 2+3 stamens); thorny (etym. thorn).— +16 species; especially ornamental shrubs, e.g. Elaeagnus argentea, angustifolia; Hippophaë rhamnoides and Shepherdia canadensis. Northern Temp. + +A small diagram showing the longitudinal section through the flower. +Flora, figs. 485-487.—Elaeagnus argentea. + +Order 3 (?). **Proceraceae** This order has its chief centre in the dry regions of Australia (?), (about of about 1,000 species), a smaller number in S. Africa (?).— +A few species have been introduced into Europe and America; they have simple stipules, and more or less dry, leathery, evergreen, and often of very different forms on the same plant (undivided, compound, etc.). The flowers are 3 +(nearly always) in a single whorl; the sepals are free or united; the +staminal-whorl ; 1 carpel; sometimes syngynous. The perianth-leaves are +generally almost free with valvate meation; often leathery. Small scales +characterize the calyx; the petals are wanting or reduced to scales. The +stamens generally have extremely short filaments, and are situated opposite, +1 compound or simple leaf-like body at the base of the pistil. The gynoecium is 1-locular, has 1- several orders, and is often raised on a stalk-like +introduc. The fruit is a follicle or nut. The seeds, most frequently winged, +have no epidermis.—Protea, Magnolia, Heliot., Eucalyptus, Grevillea, etc. + +An illustration of Elaeagnus angustifolia. +Flora, figs. 485-487.—Elaeagnus angustifolia. + +**SAXIFRAGACEAE.** + +50 genera; about 1,000 species. Several species are cultivated in our con- +servationary for the sake of the flowers, which are beautifully colored and arranged in crowded inflorescences. Prostratous. It is doubtful whether they are related to the Saxifragaceae, but the opinion that they occupy a systematic position of the order is doubtful. They are related to the Leucinaceae and Ruscaceae, but more closely no doubt to the two preceding orders. + +The flower is generally 13-17 mm. long. The corolla is usually polythalea, +usually *perigama* or *epigama*, epigama and 5-merous; most fre- +quently S5, P5, A5-5 or 3-4 and G2-5, but other numbers are found, especially 4; the flowers are very frequently obli- +gamentous, with the petals spreading from the corolla +small; the carpels in some are entirely free, in others united or less united. Endocarpus is found in the majority. The hypogynous forms approach the Cladophoræ, others the following families, especially +the Ruscaceæ and Liliaceæ, but none of them are so well developed as most of the others. The Saxifragaceæ proper, approached very near to the +homoeoecious order, are represented by the genus *Saxifraga*, of which +species known as *Philadephia*, etc., approximate the Myricaceæ. Just as the Rosal- +laean appear to be closely allied to Ricinoæ, especially *Fasciolariæ*. Finally +the *Corydalis* and *Corydalis* form a group of plants with flowers in +minutes in very reduced forms, on one hand in the arborescent order with +crowded inflorescences, on the other perhaps in the very remarkable order +*Echerraria*. + +Order I. **Crassulaceæ.** +Nearly all are herbs or small shrubs with round, succulent branches and scattered, fibrous, often more or less round leaves, which are very rarely incised, and never have stipules. The flowers are generally +typonous, dichlamydeous and cymose, +cymes, which again may be arranged in racemes, umbels, etc.; they are regular, +\(\gamma\), hypogynous or perigynous. +The frequent presence of gynae and petals (gamopetalous corollas with sessile sta- +mens) are found in *Corydalis*, *Bryophyllum*, *Echerraria*, and other genera. +In *Saxifraga* and *Glechoma* there may have +very different values, partly depending upon the size of the flower (e.g. 4-7 in +*Saxifraga*; 6-8 in *Glechoma*); but in *Saxifraga* +and *Echerraria*, the carpels are free and are placed opposite the petals (Fig. 487). Fruit a syncarp composed of follicles containing + +451 + +Fig. 487.--Diagram of a flower of *Saxifraga* (the ho- +moeocious type): 1 branch of sec- +retory gland; 2 the axis of the +trilocular fruit. + +A diagram showing a flower of Saxifraga with three locules. + +452 + +**Dicotyledoneae.** + +many, small seeds without endosperm. Outside each carpel is found a small, nectariferous scale (Fig. 487). The northern genus, *Rhodola*, is dioecious. The petal-stamens are wanting in some (*Osmunda*, *Rutafolia*), but in others they are numerous and are displayed upon their axillary branches. + +*Sulmon (Stemonocarp)* is generally 5-merous with 10 stamens ; *Senecio* pericarcius (Hosea-Locke), 12-merous, and with 24 stamens. The inner stamens are usually very rarely form bise, and also frequently exude water from the stigma. + +485 species ; occasionally Temp. (Cape, Europe). Principally used as ornamental plants. + +Order 2. Saxifragaceae. The flowers are 4-merous with 2 (-3) carpels, most frequently : S5, P5, A5 + 6 (diphyllopetalous), G2. They are regular, 3-petiolate, hypogynous, perigynous or most frequently more or less epigynous (Fig. 488). The carpels may be individually quite free, but are more frequently united at the base to form a cup-like calyx. The ovary is either mono- +1- or 2-loccular ovary, the styles, however, are always free. *Fruti* a capsule with many seeds; endosperm present.—They are herbs, most frequently with scattered leaves without stipules ; but the leaf-base is often persistent. The petals are usually wanting, and a displacement of the floral-leaves is frequent (e.g. *Chrysosplenium*...). Some Saxifragaceae, e.g. *Saxifraga*, have irregular flowers with an imperfect plane of symmetry. The petal-stamens in some may be wanting; *Hebe*, species of *Saxifraga* and *Mertensia* are ornamental in others. + +*Saxifraga* (Saxifrage) : Ss, P5, A5 + 5, G2 (Fig. 488) = capsule + +Intercornal, opening along the ventral sutures between the 2 per- +i +carpels ; the style arising from a tubule at the base of the stem.—*Chrysosplenium* (Golden Saxifrage) : 6 carpels, no corolla, 4+4 stamens ; G2. + +Proximally as most frequently found in *Saxifraga*, with the stamens successively bending towards the gynoecium; protogyny or protogyny without any movement of the stamens; *Chrysosplenium* is homogamous. + +About 100 species ; mostly in temperate regions. In Europe, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*, *Saxifraga*. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ; mostly in temperate regions. In North America, about 100 species ;mostly + +**Saxifragaceae.** 453 + +The following genera are allied to the Saxifragaceae :— + +1. *Parasium* (about 14 species ; *P. palustris*, Grass of Par- +nasus). The flower is slightly perigynous, and has 50, F5, 5 +(tertia) stamens, all free, and inserted on a short pedicel; the calyx +as barren stamindos, palmately-lobed, and (3-) 4 carpels united in a +1-loreal ovary with (3-) 4 parietal placentae. Capsule.—Protonous. +The flower has a slightly perigynous corolla, which is usually +shorter than the calyx, and in the order of sequence in which the +authors dehise: originally they lie closely round the gynoecium; the authors +dehise successively, first the outermost pair of petals, then the innermost +pair (the 5th), then the second pair, and finally the third pair (the 5th), +the filament elongating so that the latter lies over the corolla, and this is followed successively by the +4 others, until at last only one remains. The style is long and slender, and the anthers drop early, and the stigmas are not developed until this is com- +pleted. The barren stamens are palmately divided into an uneven number +(7 to 11) of segments, each segment being furnished with a glandular tip, +apparently glabrous tips; their gland-like appearance is supposed to allure +flies to visit the flower, or they may not a kind of flower which compels the +insect to visit it. The fruit is a capsule, which is dry and indehiscent; the +honey is secreted on its inner side, and not by the gland-like tips. + +2. *Adoxa moschatellina* (Moschata). This is a perennial, creeping +herb; the horizontal rhizome has an unlimited growth, and bears, +in a scattered arrangement, both foliage-leaves, and white, feathly + +Fig. 69.—Portion of Cotyledon foliolaris. b pincher-like leaf with thick corrugated edge (a) and leaf (f); f foliage-leaf of the ordinary form. + +scale-leaves. The aerial stem bears 2 opposite foliage-leaves and a +capitate inflorescence of 3 flowers, & placed internally (in opposite pairs) and 1 terminally. The flower is semi-syngynous; the calyx + +454 + +dicotyledones. + +gamosepalous, corolla absent. The stamens are divided to the base, so that each filament bears a bilocular nectary. The style is free, deeply-lobed, and with 3-5 lobes. The sepals are 3-4, 4-stamens, cleft to the base, and a 5-locular ovary. The bracts of the lateral flowers are displaced on the flower-stalk, as in *Chrysoplenium*, and united with the 2 bracteoles into a kind of 3-leaved involucre. The fruit is a berry, with a 2-celled ovary, each cell containing a single ovule with 2-locular nectaries, and a 5-locular ovary. A persistent ovule in each loculus. Fruit a drupe, green-coloured, with 1–3 stones.—This plant, which would perhaps be best placed in a special order, has also been classified under the Aralidaceae and Caprifoliaceae. +The Solanaceae (nightshade family) includes the *Solanum* (nightshade), a large genus of herbaceous plants with simple, serrated, leathery leaves. *Cucurbitaceae* (watermelon with opposite leaves), *Cephalanthaceae* (with pinnate leaves), insect-eating leaves; *Aristolochia* (fly-egg plant); *Euphorbiaceae* (spurge family). + +Order 3. Ribesales (Currants). 5-stamened Saxifragaceae with epigynous flowers.—Moderately sized shrubs with scutellate. + + +Description of the fruit of *Ribes*. +Fig. 460.--Fruit diagram. +Fig. 461.--Flower in longitudinal section. +For description see text. + + +stalked and palmented, and generally palmented leaves, with a large leaf-beat. The flowers (Figs. 460, 461), most frequently borne in racemes, are regular, epigynous, and have often, above the corolla, a cup- or bell-shaped, or tubular prolongation of the receptacle, on which the sepals, petals and stamens are situated; they have 3 sepals (opposite the sepals) and 5 petals (opposite the stamens) (opposite the sepals) and a 2-carpellate gynoecium with a multicellular ovary and parietal placenta bearing many ovoids. The fruit is a berry, whose seeds have a finely and juicy outer covering (Fig. 460). The genus *Ribes* is very large; it is found in an unbranched, or a 3-branched spinous, very closely resembling the spiny leaves of the *Hebeleia*, but which, however, are emergent springing from the base of the peduncle. *Ribes* has two kinds of tendrils: long-tendrils and short-tendrils. + +1 + +**SAXIFAGINEAE.** + +455 + +* dwarf-branches, the latter alone bearing the flowers.*—Ribes (Figs. 490–492). The blades of the leaf are folded or rolled together in vernation. *R. alpinum* is dioecious. + +7 species; especially from the N. Temp. regions (especially N. Am.).—This remarkable family is characterized by the following characters: the flower is slightly prostrateous, others are homogamous; insect- and self-pollination are found. The following are fruitful genera: *R. nigrescens* (Hodsk. Curtam.), *R. rubrum* (Linn.), *R. canadense* (Linn.), *R. nigrum* (Linn.), *R. multiflorum* (Linn.), *R. odoratum* (Linn.), and *Asia*. **ORIENTALIUM**: *Rubus*: the North American B. serratum (Golden Curtam) and *B. serpens* (White Curtam.) etc. + +Order 1. **Rosales**.—Flowers simple, opposite leaves, without stipules; flowers generally epigynous, 4-carpelous (Fig. 483).—**Euphorbia** (H.) *hurtis*, etc.). Shrubs from S. Am. and E. Asia; corolla often valvate. The following are fruitful genera: *E. lathyris* (Linn.), *E. cyparissias* (Gund.) Linn., has often irregular, large, but barren flowers in the circumference, while the others are very smaller; numerous stamens; petals usually 4, sometimes 5 or more; calyx 4-merous; in these cases it is only which in the other cases is suppressed; in the latter case the stamens are more or less suppressed. The branches of the inflorescence appear to be partially devoid of floral-buds, and are covered with a dense pubescence. + +**Pistilidae**: ramones (with terminal flower), sepals 4 (valvate), petals 4 (valvate), stamens many, and carpellary ovary 4-carpelous. + +The numerous stamens (20–30) differ by the splitting of the equal-stamens and are often therefore placed in a different order from those of the petals (Syringa, Mock Orange-Blossom), from S. Eur.; is a common ornamental shrub, as also in Denisia (Fig. 490) from N. Am. and E. Asia. + +Order 2. **Pittosporaceae**. This order has its home especially in Australia (Australia, New Zealand); it is represented by a few species of which one is a monocotyledonary tree with many ovules in a row, borne on a persistent placenta, or a bifoliate ovary. Some have berries, others capsules: *Fitzroyaurea*, *Circaea*, *Corymbia*, etc. + +Order 6. **Hamamelidaceae**. +Flowers more or less epigynous, with 5–4 P.O or 4, fertile sepals-dimama, and 4 barren petal-stamens, bilocular ovary with both carpels free or united; leaves simple or compound; flowers in cymose or panicles; 2-flowered without perianth; stamens indefinite; 2-ovule; slight or none of the petals free; fruit a berry or capsule; fruiting pedicel long, which is obtained by boiling the bark of *Lycium orientale*, from Asia Minor. +*Hamamelis virginiana* is found as berries in the Upper Colorado. + +Finally two orders with very reduced flowers are included in this family: +Order 7. **Platanaceae**. Trees, with large, sessiled, palmated and lobed + +456 +DECOTYLEDONES. + +leaves, and alternate stipules; the buds are concealed in a hollow at the base of the petiole. The bark forms a thin, smooth, brownish ring and is downy (connateous) in crowded, spherical inflorescences which are placed at wide intervals on a terminal, thin, and pendulous axis. The flowers have an insignificant calyx and corolla, the former consisting of 5 free, free carpels, 1 perianth, and 5 free petals; the latter consists of 5 free petals, 1 perianth, and 5 free stamens. Fruit a nut; endocarp absent. 5 species; frequently grown in gardens and parks. *F. occidentalis* (N. Am.), *F. grandiflora* (N. Am.). + +Order 6. Podostemaceae. Aquatic plants, especially in swiftly running water, with somewhat of a leaf-like, leaf-like, or thalloid appearance; they show almost no differentiation into stem and leaves; the leaves are usually floating (having a dorsoventral creeping stem), the flowers sunk in hollows, a formation of hairs upon the roots and thallus assimilating roots and thallus stems, etc.). Tropical. + +Family 20. *Resedaceae*. Resedineae. + +The leaves are scattered, stipulate, or have at least a well-de- veloped sheath, which is generally prolonged on each side into a free portion ("adnate stipules"). The flowers are regular, perip- gyrans or epigynous (i.e., with the pistil attached to the usual pedicel). The corolla is always polytomous. The stamens are present in very varying numbers (3–5) and position, but always placed in 5- or 10-merous whorls; they are frequently 20 in 3 whorls (*Fig. 494, 492, 503*); the stamens are placed in one or two rows along the sides of the corolla tube or more generally immersed in the bud, or even rolled up. The number of the carpels is from 1–5; in most cases all are individually free (syncarpous), and when they are united it is in every case with the corolla tube (i.e., syncarpous perigynous). The seeds have straight embryo, and usually no endocarp. + +The perianth and stamens are most frequently perigynous on the edge of the whorled receptacle; its form varies between a flat cupule and a long tube or a cup (Fig. 494). In some cases it is completely hidden beneath the surface, in some instances on a central conical elevation of the floral axis (*Fig. 492*). The corolla is often imbricate (i.e., overlapping), or revoluteate, so that it grows in and fills up the space between the carpels, so that a more or less epigynous flower is formed (*Fig. 494*). The following numbers of stamens are known: 3–5 (in 3–5 merous whorls), 8–10 (in 8–10 merous whorls), 10–20 (in 10–20 merous whorls)—compare the diagram. The theoretical explanation of this relation of the 10-merous whorls and their alternation with the 5-merous whorls may be supposed, but the development shows no indication of this, and it is not supported in any other way. Several genera have "perigynous" stamens, that is, the stipe springs from the base of the corolla (*Fig. 497 d, e*). + +1 + +**BOHEMIAE.** 457 + +The Boheemiae are on one side closely related to the Saxifragaceae (especially through Spiraea) from which it is difficult to separate them, and to the Myrti- +cea, on the other hand, from which they differ by having a much larger number of stamens, and through the Anaspalanthus with its single carpel, to the Leguminosae. The family begins with forms which have many-seeded follicles, and passes through those with one seed in a single nut and double in perigynous flowers, and on the other side to the Pomaceae. + +Order 1. **Rosaceae.** Herbs or shrubs, generally with compound leaves and persistent (adnate) stipules, flower pyriforma, gynoeceum formal of many free (therefore oblique) corollas, syncarpia, with fruits of various kinds. The exceptions are noted under the genus. + +1. **SPIREA** (Fig. 405) has 2-many ovules in each ovary, while in the other groups there is generally only 1, or never more than 2 ovules in each locule. There are generally 5 or 6 carpels and the fruit is a *follicle*, which is not enclosed by the receptacle. + +Fig. 404.—Diagram of Corolla of *Pomaceum*. +Fig. 405.—Flower of *Spiraea* insolata. + +The majority are shrubs. Stipules are often wanting. *Spiraea* (Melanthium) is a genus of beautiful plants with large, brightly +flowered inflorescences of various forms. The carpels, in some species, unite together and form a simple gynoeceum with free styles (an approach to the Pomaceae). Closer allied to Spiraea are the Ericaceae (Heath), which have a similar habit of growth, but usually nearly always double (the fruit a nut), and Rhododendron which has opposite leaves, a remarkable feature among the Boheemiae; it has a 4-merous flower, and is allied to *Rhododendron* (Erica). *Spiraea* is closely allied also to *Gillenia* (S. Am.) differing chiefly in the ascending ovules, *Spiraea* having pendulous ovules, and a more tubular receptacle. + +The following genera are included in this classification from *Spiraea* to *Pomaceum*. In the first group, which contains only trees or shrubs with generally simple leaves, the carpels are united together ; in the second group, which contains with the carpels, which are threesomes often united together ; in this case, too, the fruit is a capsule. *Quillaja* (S. Am.) ; *Eschscholzia* (China). + +Illustration showing a diagram of Corolla of *Pomaceum*. +Illustration showing a flower of *Spiraea* insolata. + +458 +DICOTYLEDONES. + +2. *Potentillae* (Figs. 494, 496, 497). The flower has an "epicalyx" (Fig. 494 C) alternating with the sepals and formed by their stigmas which are united in pairs, and hence its leaves are often more or less compound, but the calyx is usually simple and often quite insignificant. The sepals are valvate in the bud. The large number of fruticlets are adnate, borne on a well-developed convex portion of the receptacle (the Basanum resembles the Poten- +tilla, although it is a much larger plant), and are very numerous. Most of the species are herbs with dichasial inflorescences, often arranged in racemes—*Potentilla* (Cinquefoil). The achene are borne on a dry, erect, terminal style; the style is situated at the apex of the receptacle, and is surrounded by a calyx-like bract. Herbs with digitate, in some, however, pinnate leaves, and generally yellow flowers—*Conwarr* (Fig. 494) (Marsh Cinquefoil) forms, by its fluffy-spongy receptacle, a transition to the next genus—*Frageria* (Strawberry) (Fig. 495). The receptacle becomes finally flimsy, + +A 407. +Fig. 496. --Longitudinal section of flower. +Fig. 497.--Longitudinal section of flower. +Fig. 498.--Longitudinal section of flower. + +coloured, and falls off (botanically it is a berry!); the numerous fruticlets (drupes with thin pericarp) have basal styles (Fig. 407); leaves trifoliate; long, creeping runners.—*Genus* (Avena) has a terminal style; the flowers are inserted into a long, beak, which (after the upper part has been shed) bends back into a hook, thus furnishing a means of distribution for the fruits. Leaves pinnate; *Drosera* comprises 3 Arctic or Alpine species with simple leaves; *Sisyrinchium* has the same and *Saxifraga* species, the fruit resembles that of *Genus*, but the style becomes still longer and feather-like (a flying spermatophyte). + +3. *Hercule*. *Relais* (Bromus) has the same form of receptacle as the *Potentilla*, but as epicalyx; the fruticlets are drupe, not en- +closed by the persistent calyx. Most frequently shrubs or under- + +6 + +ROSIFLORE. 450 + +shrubs with prickles (emergences), glandular bristles and com- +pound leaves. In the Raspberry (R. idaeus) the fruitlets unite together and detach themselves from the receptacle. + +4. ROSE. Rose ; the receptacle is hollow, oval and contracted beneath, the calyx (Fig. 488), ultimately +fleshy and coloured ; it encloses +a large number of fruitlets at once, which are called +stones ("hip", biologically a berry).—Shrubs with impari- +nate leaves and adnate stipules (Fig. 489), namely, +the order of their development (a +divergence of B), the two orders one +on one side only, and the two +order, whose edges are covered by the +orders, are not lobed at all. Prickles +occur on the upper surface of the +fruits, but not on the lower, in a rachis- +order, being found immediately below each leaf (usually two) although some +what varying heights. + +5. AGRIMONIA. The receptacle is more or less cup- or ball- +shaped, and almost closed at the mouth ; it is persistent and en- +velopes the nut-like fruitlet but is dry, like some species hard, +the fruitlets being firmly attached to it. In biological connection + +with this the number of the carpels is generally only 1 or 2, and +the whole becomes a false nut (Fig. 500). Herba.—Agrimonia. +(Agrimony; Fig. 490, 500) the perianth is 5-morzula, stamens +3–20. The receptacle bears externally, on the upper surface, a + +Fig. 488.—Longitudinal section of flower of Rose. +Fig. 489.—Longitudinal section of flower of Rose. + +Fig. 493, 500.—Agrimonia eupatoria. +Fig. 490, 500.—Longitudinal section. + +400 + +DICTYLEDONAL. + +number of hooked bristles which serve as a means of distribution for the 1–3 achenes which are enclosed in it, and hence the entire flower finally falls off. The inflorescence is a long upright raceme. These bristles are arranged in two whorls (some authorities consider them as being in one whorl), the uppermost alternate with the sepals. *Achenella* (Ladies' Mantle, Fig. 501) has 8 green perianth-leaves in two whorls (some authorities consider them as being in one whorl), the lowermost leaves are epicalyxal, and the flower therefore apetalous), and 4 stamens alternating with the terminal whorl. There are 2 pistils, each with a basal style and central stigma. The flowers are small and greenish, the filaments jointed. The calyx is leaf-shaped entirely enveloping the stem; the leaves are glabrous, and the flower has only 1–2 stamens. The following genera, with 4-merous flowers borne in short spikes or capitula, are allied to this group. *Sanguisorba* has elongate tubular corolla, with 4 petals; *Centaurea* has a tubular corolla; *Potentilla*, spike or capitulum, the uppermost leaves are 2, the lowest 3, and some intermediate ones 3 (the order of opening is not always central); *St. John's Wort*, long spikes having broad linear stipules (genus *Hypericum*). Leaves imparipinnate. + +**FOLIATION.** A yellow ring on the inside of the leaves, inside the stem, or both. This is a characteristic of the genus, for instance, not in the case in *Rosa*, *Agrimonia*, *Spilanthes*, *S. spinulosa*, *S. arvensis*, etc., to which the insertion of leaves is not so conspicuous by the quantity of petioles. Petioles are short and slight protrusion is frequent, in which case foli- alationism also is finally possible. Potentias, with the long-haired stigma, is wind-pollinated; *Sanguisorba*, with the glabrous leaves, is insect-pollinated in all regions. **Ursus:** Ornamental: the petals of *Euphorbia cistiflorus* and *pulchra*, the fruits of the Raspberry (Rubus idaeus), the flowers of the Rose (Rosa centifolia), and those of *Quercus pubescens*. **Attar of Roses**: from *Rosa damascena*, *caninae*, and other species, especially from the southern countries; from *Rosa gallica* (the Gallic Rose), an ornamental plant; from *Rosa* Europe, Eucosma roseata (the Yellow Rose), *R. gallica* (the French Rose) and *R. rubra*; from *Wu*, Ano, *Cynara*, of which the More Rose (Cynara humilis) is a variety; from *Cynara cardunculus* and *N. Africana*, *Baccharis (the Musk Rose)*; from China, *Rosa indica* (the Rose) and its varieties; from Japan, *Rosa rugosa*; from India, *Rosa damascena*; from China, *Rosa chinensis*; from China, *Rosa multiflora*; from China, *Rosa odorata*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rosa banksiae*; from China, *Rosa chinensis*; from China, *Rossa + +BOEHFOLK. +461 + +Robin-species: Raspberry (R. fruticosa), Gooseberry (R. chamaemorus), Blackberry (R. fruticosus), etc.; & Frupea-species (Fr. ramosa, celtis, prunus, etc.). + +Order 2. Amygdalaceae. Trees or shrubs with rooseaceous flowers; leaves simple with caducous stipules; a regular, perigynous flower, the receptacle being partly hollowed out by the insertion of the petals; 5 stamens 30-30; gynoecium simple, formed of 1 carpel (hence oblique, Fig. 502), with terminal style and 2 pendulous ovoids, stipulate at their base (Fig. 503). The leaves are penninerved and frequently have glands on the stalks and edges; thorns (modified branches) often occur, i.e., dwarf- branched, or even absent. A few leaves, terminate their growth in a thorn (e.g. Prunus spinosa). The variation of the foliage-leaves varies in the different species. In Almond, Peach, Cherry, and Bird-Cherry they are folded; in the Apricot, Plum, and Fig they are erect; but in the Flowers unfolded below the leaves (Amygdalus, Armeniaca). That the gynoecium is formed of one carpel is evident from its structure (Fig. 502); also from the Laminae, which are closely related to this order, from the fact that the carpel is oblique, and has only one plane of symmetry, and similarly in the roots of these plants (Fig. 504), which are very similar in form and internal nature. It is only exceptionally that both ovaries are developed. In almond instances more than 1 carpel is developed. + +A tree of this order (R. communis, Almond-tree) has a dry pulp which is detached irregularly; when ripe, from the wrinkled, grooved, ovoid and somewhat compressed stone. + +The fruit of the Almond (Fig. 505) differs from the Almond in hav- ing a juicy pulp, not detachable from the stone, which is deeply grooved and has pits on its surface (Fig. 506). The name of the genus is derived from Persia, though it is a native of China; (Armenia) (Armenia) (Armenia). + +has a hairy, velvety fruit, but the stone is smooth and has two ribs along one of the edges; the pulp is juicy. (The generic name has been given on the incorrect assumption that it was a native of Armenia.) Home is China. + +Fig. 502—Diagram of Prunus spinosa. +Fig. 503—Diagram of Prunus spinosa. +Fig. 504—Diagram of Prunus spinosa. +Fig. 505—Fruit of the Peach. The pulp is juicy; the stone is wrinkled and ovoid. +Fig. 506—Fruit of the Almond. The pulp is juicy; the stone is smooth and has two ribs along one edge. + +402 +DECTYTYLIDONES. + +**B. Fruit GLABROUS (i.e., without hairs):* Prunus (Plum) has a glabrous fruit with bluish bloom; the stone is compressed, smooth or wrinkled. The flowers are borne solitarily or in couples, and open before the leaves. The fruits are sessile or on short stalks; they are borne on shoots without foliage-leaves.*—Corylus (Cherry), C. americana, C. chrysocarpa, C. glandulosa, C. maxima, C. maxima var. glauca, C. maxima var. purpurea, C. maxima var. rubra, C. maxima var. subintegra, C. maxima var. subintegra subsp. subintegra, C. maxima var. subintegra subsp. subintegra var. subintegra, C. maxima var. subintegra subsp. subintegra var. subintegra var. subintegra, C. maxima var. subintegra subsp. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. subintegra var. +The flowers are staminate in 2-many-flowered umbels or racemes, and open at the same time as the leaves; the petals are white or yellowish-white.*—*Laureolinum* in seed-beds are found in C. eremica (Wild Cherry), C. fruticosa (Small cultivated Cherry), from Western Asia; *moxim* occurs at the base of leaf-bearing branches and small ophiolites; *moxim* is a plant of the forest floor (blind Cherry); *C*. virginiana, *C*. laurifolia (Cherry-bush), *C*. megalocarpa, *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocarpa (Cherry-bush), *C*. megalocampa + +**Pariifolae.** 463 + +firm (the "core"). The nature of the fruit varies, according to the thickness and hardness of the endocarp, being either a "berry" or a "drupe" (see A and B). When the endocarp is thin and pulpy, as in *Pyrene* and *Cydosia*, the fruit is a berry, each of the 5 loculi generally present containing several seeds; but when this is hard the fruit resembles a drupe, only one seed is developed in each loculus, and the number of the loculi is reduced to one or two. There are nearly always 2 ovules in the loculi of the ovary, but in *Cydonia* there are a large number in 2 rows. In the genera + + +A - A stylar view of a berry. +B - A longitudinal section through the fruit of *A. Cytinum*. +C - A stylar view of a drupe. +D - A longitudinal section through the fruit of *C. Cytinum*. +E - A stylar view of a drupe. +F - A longitudinal section through the fruit of *C. Cytinum*. +G - A stylar view of a drupe. +H - A longitudinal section through the fruit of *C. Cytinum*. +I - A stylar view of a drupe. +J - A longitudinal section through the fruit of *C. Cytinum*. +K - A stylar view of a drupe. +L - A longitudinal section through the fruit of *C. Cytinum*. +M - A stylar view of a drupe. +N - A longitudinal section through the fruit of *C. Cytinum*. +O - A stylar view of a drupe. +P - A longitudinal section through the fruit of *C. Cytinum*. +Q - A stylar view of a drupe. +R - A longitudinal section through the fruit of *C. Cytinum*. +S - A stylar view of a drupe. +T - A longitudinal section through the fruit of *C. Cytinum*. +U - A stylar view of a drupe. +V - A longitudinal section through the fruit of *C. Cytinum*. +W - A stylar view of a drupe. +X - A longitudinal section through the fruit of *C. Cytinum*. +Y - A stylar view of a drupe. +Z - A longitudinal section through the fruit of *C. Cytinum*. +AA - A stylar view of a drupe. +AB - A longitudinal section through the fruit of *C. Cytinum*. +AC - A stylar view of a drupe. +AD - A longitudinal section through the fruit of *C. Cytinum*. +AE - A stylar view of a drupe. +AF - A longitudinal section through the fruit of *C. Cytinum*. +AG - A stylar view of a drupe. +AH - A longitudinal section through the fruit of *C. Cytinum*. +AI - A stylar view of a drupe. +AJ - A longitudinal section through the fruit of *C. Cytinum*. +AK - A stylar view of a drupe. +AL - A longitudinal section through the fruit of *C. Cytinum*. +AM - A stylar view of a drupe. +AN - A longitudinal section through the fruit of *C. Cytinum*. +AO - A stylar view of a drupe. +AP - A longitudinal section through the fruit of *C. Cytinum*. +AQ - A stylar view of a drupe. +AR - A longitudinal section through the fruit of *C. Cytinum*. +AS - A stylar view of a drupe. +AT - A longitudinal section through the fruit of *C. Cytinum*. +AU - A stylar view of a drupe. +AV - A longitudinal section through the fruit of *C. Cytinum*. +AW - A stylar view of a drupe. +AX - A longitudinal section through the fruit of *C. Cytinum*. +AY - A stylar view of a drupe. +AZ - A longitudinal section through the fruit of *C. Cytinum*. + +Fig., 30.—Formal diagram +of **Pyrene** parvifolia. + +Fig., 31.—Longitudinal and transverse sections through the flowers, etc., cf. **D. Cydonia**. + +which have stones, only one seed is developed in each loculus. The genera are distinguished mainly in accordance with the kind of fruit and the number of ovaries and seeds. + +**A. SORBE:** The endocarp is fleshy-soft-like or papery (drupe), with thick pericarp. + +**Pyrene** and **Cydonia**: carpels completely embedded in the cup-like receptacle, styles always free.—Pyrene: the fruit is glabrous, and has only a small calyx, withering or dehiscent, and a 5-locular ovary with at most 2 ascending ovules in each loculus. + +463 + +464 +DICYCLEOLOGES. + +loculus (Fig. 504 D). The large flowers are situated in few- +flowered umbels or corymbs. *P. communis* (Pear; free styles, Fig. 507 ; it has the well-known pear-shaped fruit; the corolla is reduced to several groups of + +Fig. 505.—Cydonia vulgaris. Longitudinal section of fruit. +sclerenchymatous cells embedded in the pulp, the leaf-stalk is as long as the blade)...*Cydonia* (Quince) has a hairy fruit with many seeds in 2 rows in each loculus of the endocarp (Figs. 504 C, F ; 506); the testa of these fruits is mucilaginous. *C. vulgaris*, large, terminal flowers on lateral branches and large leaf-like, persistent sepals. + +2 *Malus* and *Ameles- +chier* (*Aronia*), carpels free on the ventral edge; styles united. +*Malus* *crab-apple* +(Apple) "fruit" is "uni- +biligate" at the base; no +sclerenchymatous cells in +the pulp; styles united at + +Fig. 507.—Longitudinal section of Pear flower. + +**ECHINOFORE.** 465 + +the base (Fig. 504 D); leaf-stalk shorter than the blade. *Sorbus* (Mountain-ash) differs only in having a 2–3-sepalate fruit with extremely thin endocarp. Cymose inflorescences in umbellate cymes. *S. europaea* has plume leaves, *S. arctica* (White-beam) and other species have simple leaves. The flowers are sessile on a short divi- +sional wall springing from the dorsal axile, and more or less projecting into each of the lobes of the ovary; *Zapotaceae* (Fig. 501 E) has racemes and a single flower. + +**B. CHAETACEAE.** The **exocarp** is hard and dense ("drupe"), generally with several, sometimes, however, with only 1–2 stones, rarely one multilocular stone; only 1 seed in each of the bouni— +*Crataegus* (Hawthorn, May). There are 1–3 stones in the spherical or ovoid fruit. The dune, found on the apex of the fruit, inside which the stone is placed, is called the "pulp" (Fig. 504 A, B, traverse section of the fruit). Shrubs with thorns (branching) and mode- +rately large flowers borne in corymbs—*Mespilus* (Medlar) differs from the fast-named only in having a large dune at the apex of the fruit, and in having a stone in each of its lobes, but not in +the greatest diameter of the fruit. The flowers are solitary and ter- +minal—*Cotoneaster* is chiefly distinguished from the others by its syncarpy, the 2–3 carpels (and stones) being free from one another by a short stalk; also by its leaves being opposite or alternate portion of their dorsal surface (Figs. 504 A, B), so that shrubs with leathery leaves, generally covered with white, fatted hairs on the lower surface, and with small flowers; the fruit is red or black. + +Pear, Apple, Mountain Ash and Hawthorn have profuseous flowers which reach their maximum development during the summer months; in the northern temperate regions—Pear and Apple are especially cultivated for this purpose; they are grown in many parts of Europe ; especially in southern countries also the Quince (from N. Persia and the Caucasian districts), Medlar and *Cotoneaster vulgaris*. Many species (Caninae), such as *Prunus avium*, *P. cerasifera*, *P. spinosa*, etc., whose name is derived from the Apple-tree— *M. esculenta*, which grows wild in European forests, appears to have been less used. The early Lake-dwellers in Switzerland had the apple- +tree as their chief food-supply; it was probably introduced into Europe to be +*Pyrus* *avium* (Central Asia). Many of the species of *Cotoneaster*, some with double +flowers, and *Pyrus* (Cherrywood) japonica, with brilliant red flowers, are culti- +vated for ornamental purposes; they are often planted near the +south-western trees. The fruit contains free organic acids and sugar; prune +may be obtained from the seeds. The wood of the Pear tree is used in +many structures. + +
JuncaceaeDescription285 + +**Glenioflore** + +annual) herbs living in damp situations, with a symmetrical rhizome and grass-like appearance. The stems are seldom hollow, or have swollen nodes, but generally *triramous*, with the upper internode often arranged in 3 rows, the leaf-blade is closed (very seldom open), and the leaves are usually simple. The leaves are arranged in 2 rows, the leaf-blade is closed (very seldom open), and the leaves are usually simple. The leaves are arranged in 2 rows, the leaf-blade is closed (very seldom open), and the leaves are usually simple. The leaves are arranged in 2 rows, the leaf-blade is closed (very seldom open), and the leaves are usually simple. + +The flowers are supported by a bract, but have no flower-stalks (Fig. 284 A). The perianth is distinctly represented by six bristles corresponding to six leaves (Figs. 284 A, 480 D); in other respects it is wanting. There is an indefinite number of hairs (Fig. 284 B), and very frequently it is altogether wanting. The upper bristle is called a *spikelet* (Fig. 284 B). In the flower there are therefore 3 stamens (nearly more or less than 3), the anthers are attached by their bases to the filament (immate) and are not bled (Fig. 280). Gynecium simple, formed of 3 or 2 carpels; 1 style, which is divided at the extremity into two branches; ovary with 3 loculi; each locus of the ovary contains one basal, erect, anatropous ovule; the stigmae are not feather-like. Fruit a pod, whose seed is generally united with the pericarp. The embryo is small, and lies at the base of the seed-capsule, on its ventral side by the endosperm (Fig. 280 B). On germination the cotyledon does not remain in the seed. + +A regular perianth, with 6 scale-like perianth-leaves in 2 whorls, is found in *Orolobus*. In *Scirpus* *littoralis* the perianth-leaves are spreading at the apex, and their bases are united. + +The branching of the inflorescence is often as in the Juncaceae, and supports the theory that these two orders are related. In *Bergschadenia* and others, this arrangement is also found to be some extent composite. + +**A. Spikelot. Hemantophytes Flores.* + +1. Spikelots cylindrical, the bracts arranged spirally (in many rows). The lower ones are often barren, each of the others supports a flower.--*Scorpio* (Club-rush). The spikelots are knobbed or conical, or sometimes flat; they do not continue to grow during the ripening of the fruit (Fig. 280 A). Closely allied to this is *Holocarion*, with terminal spikelots.-- + +A diagram showing the structure of a Glenioflora species. +A B C D + +280. +MONOCOTYLEDONS. + +**Eriophorum (Cotton-grass)** differs chiefly in having the perianth- +bares prolonged, and forming a bunch of white, woody hairs (Fig. +284 H). + +**Cladium** and **Elymus** (Bog-rush) differ especially in the free-flowered, +compound spikelets which are collected into small bunches; the latter has +reverted to the former condition, but the lowermost portion of the style remains +attached to the fruit in a base. + +2. Spikelets compressed, the bracts arranged only in two rows; the other characters as in the first-mentioned. *Cyperus* (spikelets many-flowered); *Scheelea* (Dog-rush); *Galeobdolon* few-flowered; *S. nigricans* (Black-sedge). + +B. **Cariceae. Unisexual flowers.** + +In the *C. flores* there is no trace of a carpel, and in the 2 +no trace of a stamen. Floral-leaves in many rows. In some +(*Scirpus*, e.g., *S. lacustris*) the leaves are alternate, borne in +the same spikelet, the latter at the base or the reverse; in the majority +each spikelet is unisexual. + +*Corys* (Fig. 285) has naked, most frequently monocious flowers. +The ?-spikes, which are generally placed at the summit of the +whole compound inflorescence, are not compound; in the axil of +each floral-leaf (bract) a flower is borne, consisting of a short + + +A: A female flower with 3 stigmas. +B: A male flower with 1 stigma. +C: A female flower with 1 stigma. +D: A male flower with 1 stigma. +E: A female flower with 3 stigmas. +F: A male flower with 1 stigma. +G: A female flower with 3 stigmas. +H: A male flower with 1 stigma. +I: A female flower with 3 stigmas. +J: A male flower with 1 stigma. +K: A female flower with 3 stigmas. +L: A male flower with 1 stigma. +M: A female flower with 3 stigmas. +N: A male flower with 1 stigma. +O: A female flower with 3 stigmas. +P: A male flower with 1 stigma. +Q: A female flower with 3 stigmas. +R: A male flower with 1 stigma. +S: A female flower with 3 stigmas. +T: A male flower with 1 stigma. +U: A female flower with 3 stigmas. +V: A male flower with 1 stigma. +W: A female flower with 3 stigmas. +X: A male flower with 1 stigma. +Y: A female flower with 3 stigmas. +Z: A male flower with 1 stigma. +AA: A female flower with 3 stigmas. +BB: A male flower with 1 stigma. +CC: A female flower with 3 stigmas. +DD: A male flower with 1 stigma. +EE: A female flower with 3 stigmas. +FF: A male flower with 1 stigma. +GG: A female flower with 3 stigmas. +HH: A male flower with 1 stigma. +II: A female flower with 3 stigmas. +JJ: A male flower with 1 stigma. +KK: A female flower with 3 stigmas. +LL: A male flower with 1 stigma. +MM: A female flower with 3 stigmas. +NN: A male flower with 1 stigma. +OO: A female flower with 3 stigmas. +PP: A male flower with 1 stigma. +QQ: A female flower with 3 stigmas. +RR: A male flower with 1 stigma. +SS: A female flower with 3 stigmas. +TT: A male flower with 1 stigma. +UU: A female flower with 3 stigmas. +VV: A male flower with 1 stigma. +WW: A female flower with 3 stigmas. +XX: A male flower with 1 stigma. +YY: A female flower with 3 stigmas. +ZZ: A male flower with 1 stigma. +AAAAA: Female flowers each bearing one leaf, namely, a two-keeled fore-leaf +BBBBB: Male flowers each bearing one leaf, namely, a two-keeled fore-leaf +CCCCC: Female flowers each bearing one leaf, namely, a two-keeled fore-leaf +DDDDD: Male flowers each bearing one leaf, namely, a two-keeled fore-leaf +EEEEEE: Female flowers each bearing one leaf, namely, a two-keeled fore-leaf +FFFFFFF: Male flowers each bearing one leaf, namely, a two-keeled fore-leaf +GGGGGGG: Female flowers each bearing one leaf, namely, a two-keeled fore-leaf +HHHHHHH: Male flowers each bearing one leaf, namely, a two-keeled fore-leaf +IIIIIIIJJKKKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOOPPPQQQQQRRRSSSTTTUUUVVWWWWWXXXYYYZZZZZAAAAABBBBCCCDDDEEFFFGGGGHHIIIJJKKKKLLMMNNOOO + +257 + +(Scirpus, etc., in the figures) which is turned posteriorly (as the two-leaves of the other Monocotyledons), and being obliquely sheath-like, envelops the branch (in the same manner as the sheath of the vegetative leaves), and forms a pitcher-like body. In the axil of this leaf the 2-flower is situated as a branch of the 3rd order, bearing one or two flowers, which are enclosed in one greenish-yellow style-like body, through the month of April-March. + +The axis of this order (in fig. 280 D) may sometimes elongate as a brachy-like projection (usually in Uncinia, in which it ends as a hook, because it is supported by a long stalk). The 2-flower of this vine-leaf bears 1-3 branches which support male-flowers, this is normal in Euphorbia (or Kewendii) and Schenkiatulips; the axis (or stem) bears at its base a female flower supported by this structure, and beside it a male-flower supported by its bract. + +**Foliation** by means of the wind. Frequentous. Sometimes self-pollinated. +The only species of this order that are known to be pollinated by wind: Carex and Scirpus are most numerous in cold and temperate climates, and become scarce in warm regions. The 2-flower of Carex is usually pendulous. Carex and other tropical genera. They generally confine themselves to snow, swampsy districts, some on the other hand, are characteristic of sand-dunes, such as Ficaria, etc., and some on the other hand, are characteristic of marshes, such as Utricularia. + +Urnus. In spite of their large number, the Cyperaceae are of no importance as fodder grasses, as they are dry and contain a large amount of silica; hence the edges of their leaves are often cut with a knife to remove this sharp cutting. **Cyperus esculentus** has tubercles rhizomes, which contain a large amount of fatty oil and are edible (naturally); it has its home in the continent of Africa. + +**Cyperus papyrus** (W.A., Egypt, Sicily) attacks a height of several meters, and has stems of the thickness of an arm which were used by the ancient Egyptians for writing on them. **Cyperus rotundus** (the "corm" or "tubercle"), etc. Is an ornamental plant. + +Order 3. Graminear (Grasses). The stems are cylindrical, generally hollow with swollen nodes, that is, a swelling is found at the base of each leaf which apparently belongs to the stem, but in reality it is the swollen base of the leaf. The leaves are usually alternate (except in some species of *Eriogonum*, *Tricholaena*, *Tricholaena*, etc., in which the sheath is not split), and the edges overlap alternately, the right over the left, and vice versa; the ligule is nearly always well developed. In general, the flowers are solitary or in cymes; in some cases there areinate floral-leaves, and the spiklets thalameres are borne in either spikes or panicles. The two (soldem) lower floral-leaves in each spikelet (fig. 280 Y, x, z) are barren (as the covering-leaves in many umbels and capitula); these are termed the glanses. The + +U + +288 +MONOCOTYLEDONES. + +succeeding floral-leaves, each of which supports one flower as its bract, are called the outer pala (a); these sometimes each bear an "awn" (a bristle-like body which projects in the median line either from the apex or the back); sometimes the upper ones are barren. Each flower has two sepals, which are united on the inside opposite the main axis; it is thin, becoming a two-lobed awn as an awn; it is known as the inner pala (b). Immediately succeeding the bractole are: (a) some small, delicate scales (Indiferae, Figs. 287 D, 288 C, 290 L); (b) a single, long, narrow leaf-like scale, so as to be somewhat similar to a bract, and usually notched at each end (Fig. 287 O); and (c) a simple gynoeceum formed of one corpet with two styles having generally spirally-branched stigmas (Figs. 287 D, 288 C). The ovary is sessile and pendulous, and contains one ascending or pendulous and one ovate or ovoid seed. The seed is very firmly united with the thin pericarp ("carposperm"). The embryo is + + +A. Longitudinal section of fruit showing the notch where the epicalyx was inserted; B. An entire epicalyx; C. A flower with the pala; D. A flower without the pala. + + +Fig. 287.—Trillium. A note (notebook) of ear showing the notch where the epicalyx was inserted; B an entire epicalyx; C a flower with the pala; D a flower without the pala. +I. Longitudinal section of fruit. +II. Transverse section of fruit. +III. Longitudinal section of fruit. +IV. Transverse section of fruit. +V. Longitudinal section of fruit. +VI. Transverse section of fruit. +VII. Longitudinal section of fruit. +VIII. Transverse section of fruit. +IX. Longitudinal section of fruit. +X. Transverse section of fruit. +XI. Longitudinal section of fruit. +XII. Transverse section of fruit. +XIII. Longitudinal section of fruit. +XIV. Transverse section of fruit. +XV. Longitudinal section of fruit. +XVI. Transverse section of fruit. +XVII. Longitudinal section of fruit. +XVIII. Transverse section of fruit. +XIX. Longitudinal section of fruit. +XX. Transverse section of fruit. +XXI. Longitudinal section of fruit. +XXII. Transverse section of fruit. +XXIII. Longitudinal section of fruit. +XXIV. Transverse section of fruit. +XXV. Longitudinal section of fruit. +XXVI. Transverse section of fruit. +XXVII. Longitudinal section of fruit. +XXVIII. Transverse section of fruit. +XXIX. Longitudinal section of fruit. +XXX. Transverse section of fruit. +XXXI. Longitudinal section of fruit. +XXXII. Transverse section of fruit. +XXXIII. Longitudinal section of fruit. +XXXIV. Transverse section of fruit. +XXXV. Longitudinal section of fruit. +XXXVI. Transverse section of fruit. +XXXVII. Longitudinal section of fruit. +XXXVIII. Transverse section of fruit. +XXXIX. Longitudinal section of fruit. +XL. Transverse section of fruit. + +larger than in the Cyperaceae and is placed at the base of the seed, but on the outer coruse surface of the pericarp (Figs. 287 I, 28S + +GLUMIFLORE. 289 + +288 (p. 291), outside the endocarp; plenum large with several leaf-prismatic. On germination the cotyledon remains in the seed. +The majority of Grasses are annual or perennial herbs; tree-like forms being only found in the Tropics, for example, the Bamboo (Bambusus, which in fact, is not a true tree) and the palm of the basil-leaves, while the leaves are borne higher than the stem are separated by longer internodes and have no vegetative branches in + + +A - Inflorescence; +B - The uppermost flower of a spikelet, with its bracts and pedicel; C - The lowermost flower of a two-keeled inner pale (bract) and the elongated outer pale (bract); D - The lowermost flower of a three-keeled inner pale (bract); E - One corner with five stamens on the inner pale; F - One corner with four stamens on the inner pale; G - One corner with three stamens; H - The fruit seen from the dorsal side; I - The same seen from the ventral side. + + + +Diagrammatic outline of a spikelet: A lower glume; B upper glume; C lower pale; D upper pale; E inner pale; F outer pale; G lower lemma; H upper lemma; I lower lobe; J upper lobe. + + +Fig. 231.—Bamboo spadix. A Inflorescence; B one uppermost flower of a spikelet, with its bracts and pedicel; C one lowermost flower of a two-keeled inner pale (bract) and the elongated outer pale (bract); D one corner with five stamens on the inner pale; E one corner with four stamens on the inner pale; F one corner with three stamens; G the fruit seen from the dorsal side; H the same seen from the ventral side. + + +Fig. 230.—Diagrammatic outline of a spikelet: A lower glume; B upper glume; C lower pale; D upper pale; E inner pale; F outer pale; G lower lemma; H upper lemma; I lower lobe; J upper lobe. + +Only a few Grasses have a solid stem, such as Maize, Sugar-cane, and Andro- +pagos. The blade is flat in the meadow-grasses, but the Granes which live on dry places ("prairie-grass") exposed to the sun, often have the blade tightly + +290 +MONOCOTYLEDONES. + +rolled up and almost filiform or bristle-like, with anomalous anatomical structure. A closed tubular sheath is found in *Zelkova uniflora*, *Bassia-speciosa*, *Ficus petiolaris* and *triloba*, *Brassica* and some *Glyceria-species*. The sheath is developed into a long, narrow, cylindrical tube which is prolonged into a stalk. The "nodes" (the swollen points which are seen on stem of grasses) are also present in the sheath. The sheath is at the base of the leaf-sheath. They play a part in assisting the lamina to regain its vertical position when laid prostrate by wind or rain. The stem on the pale is homologous with the leaf-sheath, but the leaf-sheath is not homologous with the stem. The arrangement of the leaves in the *spadix* is similar to that in *Cyperus* and other Cyperaceae, their distal-leaves being borne in several rows in interstices. More than two rows of leaves are often present in the *spadix* of *Cyperus* and others. The spikelets, too, are again arranged in two rows in the axis of compressed floral-leaves. The inflorescence becomes a "compound spike" (ear), when + + +A diagram showing the arrangement of the leaves in the *spadix* of *Cyperus*. + + +**Fig. 290.—Diagram of the *spadix* of *Cyperus*.* +290 + +**Fig. 291.—Longitudinal section of an Ophiogomum.*
+One-leaf: a—the skin (hypodermis and epidermis); b—the vascular bundle;
+c—the phloem. + +the spikelets are remote. In the majority of instances the spikelets are borne on long stalks (pedicels). These, however, may be short or even absent. Frequently all branches of higher order, are placed so far down upon the mother-axis that they all appear to be equal valued and to arise in a semicircle from the mother-axis itself, thus forming a "compound spike". This is seen in many species of *Cyperus*. Sometimes the main axis and branches of different orders unite together as in *Elymus*. Phleum, and some other Gramas, and hence the single (short-stalked) panicle of *Pennisetum*. In these cases the lower parts of the inflorescence are dark-colored, directly from the main axis, with the production of a paler-colored inflorescence bearing "head-like" panicles. In this case we have a "compound inflorescence", somewhat different from the "ear". The flower is rarely unisexual (two sexes) or barren. Considerable difficulty is experienced in reducing the Grass- + +GLUMIFLORUS. + +flavor to the ordinary 3-merous Monocotyledonous type. Some authorities consider the indusium, which are present in all genera but absent in the Cyperaceae, to be homologous with a perianth. According to a more recent theory, however, the indusium is a modification of the bracteole (Fig. 270). In the Juncaceae, have 5-3 bracteoles placed in two rows in the median plane. If this theory be correct, the flower is naked. The bracteoles expand quickly and cause the stamens to be exposed. This is also true of some other families (see next chapter). Generally only one stamen belonging to the outer whorl are present (Fig. 269), as in Iris (Fig. 270), certain Juncusseae and Cyperaceae (Fig. 269), but in some, such as Carex (Fig. 270) and Sphagnum (Fig. 270), two are found. +Juncusseae has more than six. Only 3 of the carpels are present, namely, the +antheridia (of those in Fig. 270) and the style, and the place of at- +tachment of these organs is indicated at the back of the ovary. The number of +styles does not correspond with the number of carpels, and the styles may therefore be regarded as modified bracteoles. The position of the inner whorl—a +position which is not without analogy. In addition, a stigmal projection is some- +times found on the anterior side and in the median line (e.g., in Phalaris), and +the style may be prolonged into a long filament. This arrangement +is found in some species of Juncusseae which have only one style; other +species of Juncusseae have three styles. A triplicate style is found in Phalaris, +Cyperaceae, and Carex (Fig. 270). The flowers are usually sessile on a type +tion.—The outer pale is at the base of the flower since it bears its axis in its axial +floral shoot; the inner pale occupies the customary position of the bracteole. +The first pale is often represented by a short pedicel which supports +the main axis during development. Similar biserial bracteoles are found in +Iris (Fig. 270). These bracteoles in both Grasses and Iris arise from single pri- +mordia, while in Juncusseae they arise from several primordia. The styles +are only the parts of the remains of the outer whorl having been cap- +sulated by the inner whorl. The style is usually long and slender; it is +however, found in the Rice and some species of Gramineae. The color whorl of +stamens is usually absent, though this again is present in the Rice and Ramson. +The flowers are usually perfect, but sometimes unisexual (see next chapter). +The FLORALFORMS. In the panicled flowers open in basalial order; the flowers in the spikelet situated somewhat above the middle, commence to open from below upwards; or, finally, all open simultaneously (as in Grasses) +never open over (dehiscent); Lecreis arundinacea, Spica-species, and e.g., +Wheat and Rice in cold damp weather; some open their pales so wide that the +authorities say that they are opened by wind; others open their petals when +the pistils expand and force the pales widely apart. The filaments elongate +considerably before anthesis; thus, in Carex, they are very long before anthesis. +Pollination is generally effected by the wind. The pales separate the pales +very early; thus, in Carex, they remain together until anthesis; in Phalaris, +it is almost entirely sterile when self-pollinated. The pales flower at any +time of the day, each flower lasting only a quarter of an hour. The pales open +each other after anthesis; thus, in Carex, they remain closed until anthesis in +their own flower and two-thirds outside. Self pollination is effective, but +crossing gives better results. In Hordeum vulgare (all flowers *) the flowers + +202 +**BIOGEOGRAPHICAL NOTES.** + +of the 4 outer rows below as in the Wheat, but those in the two central rows always remain closed. The 7 downy in the two central rows of H. distichus remain closed and fertilize themselves; they open exceptionally, and may be pollinated by insects, but are not fertilized by internal nect. H. hirsutum is dioce- +mic. Cots pollinate themselves. + +The ripe *Grass-fruits* in some species of Bamboo, in a berry; in some other Grasses in a pod; in some species of *Caryophyllaceae* (e.g., *Caryophyllum*) a pericarp is "encaryopis". In some instances it is loosely enveloped by the pales (Oat), in others firmly attached to them (Barley), and finally, in others, "unaked", e.g., it is entirely free from the pales (Wheat and Elym). On the ventral side there is a + +A diagram showing the structure of a grain of wheat. + +Fig. 365.—Birching grain: A sec- +tion through the grain, showing +the most external part of the exo- +carp (i.e., the pales) and the +endosperm (ii); also the endo- +carp-enclosing layer; a. starch +grain; b. starch-containing cell; +c. starch-containing cell with +starch grains; d. starch-grain. +See text. + +Fig. 366.—Whatev- +er grain, showing the +plumule (i) the first +leaf (ii) and the second +(tergon), i.e., the primary +cotyledon; also the endo- +carp-enclosing layer. +See text. + +Fig. 367.—Unopened +grain of Wheat: a. starchy +layer; b. endosperm; c. starch +grain; d. starch-containing +cell with starch grains; e. +starch-containing cell without +starch grains; f. starch- +containing cell with starch +grains; g. starch-containing +cell without starch grains; +h. starch-containing cell with +starch grains; i. starch- +containing cell without starch +grains; j. starch-containing +cell with starch grains; k. +starch-containing cell without +starch grains; l. starch- +containing cell with starch +grains; m. starch-containing +cell without starch grains; +n. starch-containing cell with +starch grains; o. starch- +containing cell without starch +grains; p. starch-containing +cell with starch grains; q. +starch-containing cell without +starch grains; r. starch- +containing cell with starch +grains; s. starch-containing +cell without starch grains; +t. starch-containing cell with +starch grains; u. starch- +containing cell without starch +grains; v. starch-containing +cell with starch grains; w. +starch-containing cell without +starch grains; x. starch- +containing cell with starch +grains; y. starch-containing +cell without starch grains; +z. starch-containing cell with +starch grains. + +The endosperm is composed of two layers: an inner one, which contains the embryo and its food-stuffs, and an outer one, which contains only food-stuffs, but no embryo (Fig. 368 F). The inner layer is formed by a large number of cells, each containing a single embryo (Fig. 368 F). The outer layer is formed by a large number of cells, each containing a single embryo (Fig. 368 F). The inner layer is formed by a large number of cells, each containing a single embryo (Fig. 368 F). The outer layer is formed by a large number of cells, each containing a single embryo (Fig. 368 F). + +The embryo consists of three parts: a plumule (i), a leaf (ii), and a tergon (iii). The plumule is the first part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The leaf is the second part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The tergon is the third part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). + +The embryo consists of three parts: a plumule (i), a leaf (ii), and a tergon (iii). The plumule is the first part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The leaf is the second part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The tergon is the third part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). + +The embryo consists of three parts: a plumule (i), a leaf (ii), and a tergon (iii). The plumule is the first part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The leaf is the second part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The tergon is the third part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). + +The embryo consists of three parts: a plumule (i), a leaf (ii), and a tergon (iii). The plumule is the first part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The leaf is the second part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The tergon is the third part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). + +The embryo consists of three parts: a plumule (i), a leaf (ii), and a tergon (iii). The plumule is the first part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The leaf is the second part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The tergon is the third part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). + +The embryo consists of three parts: a plumule (i), a leaf (ii), and a tergon (iii). The plumule is the first part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The leaf is the second part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The tergon is the third part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). + +The embryo consists of three parts: a plumule (i), a leaf (ii), and a tergon (iii). The plumule is the first part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The leaf is the second part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The tergon is the third part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). + +The embryo consists of three parts: a plumule (i), a leaf (ii), and a tergon (iii). The plumule is the first part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The leaf is the second part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The tergon is the third part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). + +The embryo consists of three parts: a plumule (i), a leaf (ii), and a tergon (iii). The plumule is the first part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The leaf is the second part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The tergon is the third part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). + +The embryo consists of three parts: a plumule (i), a leaf (ii), and a tergon (iii). The plumule is the first part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The leaf is the second part to emerge from the seed, and it is usually covered by a protective sheath (Fig. 368 F). The tergon is the third part to emerge from + +GLUMIFLORE. +203 + +dissolves the endosperm by means of the peculiar epithelial cells developed on the dorsal surface. The radicle, on germination, is obliged to perforate a mass of cells derived from the suspensor and which forms the "coenocyst" (coenocystus = coenocytic). The latter is frequently developed before germination; these quickly break through, and take on an ellipsoid form by which they appear at the base of the leaf (Fig. 295, 294). + +The occurrence of the fruit is most frequently affected by the wind. The spiny fruits are carried away by the wind, and are dispersed by the rain (Arvena, Silene, etc.) assisted in their dissemination, and even helps to bury them in the ground. + +The two kinds of glumes are more closely related to each other than they are to the Gramineae. + +The generic differences are chiefly founded on the form of the inflorescence, the number of florets in the drawers in the culmlets, the shape and relative length of the blades, awns, etc. In addition to these the structure of the fruit differs greatly. Some have a very great many florets; some have compressed starchy grains, while others have few. Some have large or almost linear culmlets, others have long culmlets (Fig. 292), etc. + +I. BARESEAE. Tall Grasses with woody, very silkyulous stems which bear many branches in the axils of the leaves. 6 stamens. Stenotus (Bambusa). + +2. OXALIDEAE. Organ suave (Rice) is a herbaceous marsh-plant, with small panicles; 1-flowered spikelets, with two small glumes and two large, boat-shaped, strongly silkyulous pales. 6 stamens. + +—Leucoria. Lepirona. Zizania aquatica. + +3. MAJESTICAE. Maize (Indian-corn, Maize); the spikelets are minute; the 9-spikelike panicles are composed of 3-4 spikelike branches; the 9-spikelike closely crowded and arranged in many rows in a thick, axillary spike, enclosed by large sheathing-leaves. The 2-spikelike are (1-2) flowered; the ovary bears one, long filamentous style, with a broad stigma. + +4. ANDROGOGOAE. Saccharum (Sugar-cane); the spikelets are exceptionally small, 1-flowered, and borne in pairs in many-flowered, long-hairied panicles. Tall grasses with solid, sappy stems. + +5. FESTUCACEAE. Grasses with panicle (or spike-like panicle) and several-flowered spikelets. Glumes small, in each case shorter than the spikelet.—Festuca (Fescue) and Bromus (Brome, Fig. 293) have a single leaf-sheath at the base of each panicle slightly below it. Festuca has perennial species, with only a sparsely-branched panicle with branches solitary or in pairs, and round spikelets; the leaf-sheath is widely open. Bromus has the + +204 +**MONOCOTYLEDONES** + +branches borne in half whorls, and the leaf-sheath scarcely half open. *Bryophyllum* has very short-stalked spikelets in a raceme. +—*Itea* (Mint) and *Caryopteris* (Barberry) have awl-shaped spikelets; these in *tea* are oval, compressed, and with sharply-keeled glumes; in *Barberry* they are broad, cordate and drooping, with boat-shaped glumes; in *Gloriosa* round, long, many-flowered, and with a long peduncle. —*Dactylis* (Cow's-foot) differs from all others in the somewhat crowded and unilateral (subumbellate) spikelets, which are compressed and oblique (cf. one side more convex than the other). +—*Phalaris* (Rye-grass) has the spikelet on a short stalk; the spikelet is $g$; its axis is covered with long, silky hairs; panes without awns, but acuminate. Perennial marsh-plants—*Melica*; panicle small, sparsely-branched with round, awnless, few-flowered, usually drooping panicles; *Melica* has upper panicles, with numerous flowers, yet generally clustered into a cyme—*Melica*. —*Eriophorum*, *Koeleria*, *Catabrosa*, *Cynurus* (Dog's tail)—has a small spikelet panicle with unilateral spikelets, some of which are fertile, some barren, each supported by a pectinate scale. —*Arundo*. *Sesleria*. *Zimmermannia*. *Tetrapogon*. + +6. **AVENELLA** Panicles with 2-many-drooped spikelets; at least one of the glumes is quite as long as the entire spikelet.—Avena (Oats). The panicles are usually broad, and at about the middle of the back has a twisted bent stem. *Hypochaeris* has a long-branched panicle with small, 2-flowered spikelets; the pale has a dentate apex and bears an awn on the posterior side close to the base—*Wing-orchid*. *Holcus* (Yorkshire-fir); a soft, hairy Grass with a long-branched, long-stalked glume; the spikelet of which the lower one is $g$, the upper $g$; the pale which supports the $q$-flower has no awn, but that which supports the $d$-flower, on the contrary, is awned. + +7. **Amaranthus** Panicles with 1-many spikelets; panicles with flowered spikelets. Generally 2 glumes and only 1 pale.—The following have *Panicum*: *Milium* with square panicle-branches and round spikelets; *Amaranta* (Flax), with compressed, glabrous spikelets, whose glumes are narrow and pointed; *Amaranta* (Flax), having a sheath of long hairs at the base of the pale—*Stipa* (Feather-grass) has a long twisted awn.—The following have spike- +like panicles: *Pheum* (Lamb-tail), *Timothy grass* has sharply pointed, entirely free glumes, which are much longer than the awnless pale. —*Alfalfa* (Fodder-grass): glumes united below; pale + +GLUMIFLORE. 205 + +with awn. *Anemophila (Panama) . arundinacea*; pale hairy at base; perennal, self-leaved, glaucous and grass-like creeping rhizome. *Aristida*. *Sporobolus*. + +7. *Phalaride*. Panicoid spike-like panicles. The spike-let has in the upper pair a single fertile flower; below it are phleoid flowers. The lower 1–2 sometimes support 2–3 flowers. On the whole, 6-flower-leaves of the first order are present.—*Phalaris (P. canariensis, Canary-grass)* has an ovate, spike-like panicle, the spikelets are compressed, convex on the outer side, concave on the inner side. The inner glume is wrinkled on the back.—*Dipogon (A. arundinacea)* is closely allied to *Phalaris*, but the keel of the glumes is not winged.—*Autotrichia* (*A. obtusa, Sweet-vernon*) has a small, lanceolate, open, spike-like panicle with 2–3 flowers; the lower leaves, and above these an 3-flower with 2 stamens. The upper glume is longer than the flower.—*Hierochloa*. + +8. *Cynodon*. The spikelets are arranged in the form of a spike in two rows on each side of the axis; the lower row is usually more than one-flowered. + +—*Chloris ; Ctenium ; Cyamum ; Elemurus ; Microchloa*. + +9. *Pancra*. The spikelets are borne in panicles or spikes, which may be arranged like fingers or in a raceme. There is a centrally-glazed $q$-flower; below it are 2–3 sterile flowers. *Cynodon* has an almost cylindrical spike-like panicle with several barren branches, which project as stiff, rough bristles.—*Cynodon ; Pentameris*. + +11. *Hordea*. Spikes compound; spikelets sessile in the notches of a toothed leaf. + +A. Spikelets solitary.—*Trifolium (Wheat, Fig. 25)* is in each tooth of the main axis, a several-developed spikelet, which turns its flat side towards the central axis. The cultivated species (true Wheat) are 2–3 annuals, the wild ones (T. repens, Grass), also as many as infinite; they have a slender rhizome with spreading rhizome and lanceolate glumes.—*Lolium (Rye-grass)* has in each tooth of the main axis a many-flowered, compressed spikelet, which is placed adaxially on the lateral branch; except of $q$, perennals have only one outwardly-turned glume (*A. arundinacea* has a rudiment of $q$-flower inwardly-turned lower glume); the terminal spikelet has two glumes.—*Scilla (Rye). A two-flowered spikelet in each tooth : lanceolate, lanceolate, acuminate glumes.* *Nardus* and *Leymus* have very narrow spikes, the former with unilateral spikelets. + +B. In each notch of the axis 2 or more spikelets are placed + +206 + +BUNOGOUTYLEDONES. + +close together—*Hordeum* (Barley). In each tooth three 1-flowered spikelets. *H. hemicanzus* (2-rowed Barley), has 6 rows of fruits, since all the spikelets are fertile, and *H. distachium* (2-rowed Barley) 2 rows, since the lateral spikelets are barren (p. 202)—Elymus (Elymus) has 3-5 fertile spikelets in each joint of the main axis. *Aegilops* has spines upon the glumes. + +**Distribution.** 313 genera with 8,500 species. The order is distributed over the whole world, and as regards number of individuals in perhaps the richest countries, we have to mention: *Cynodon* (Sod-grass), *Lolium* (Lyme-grass), *Oryza* (Olive-grass, Avena, Avenastrum, etc.; in E., Europe, Avena domesticus); in England, next to the Compositae, it is the order most rich in species (about 150)—The origin of this order is unknown; it is supposed that it was introduced by man, but it is indigeneous to America, where its nearest relatives are found, and where it has also been discovered in ancient Indian gardens; *Dura* or Gruenin- +geria, *Rumex* (Rumex), *Cynodon* (Sod-grass), and *Avena* (Oat-grass) have doms primarily from Western Asia and South-Eastern Europe (hady from Armenia and Persia, where a very closely related wild species is found). The genus *Avena* is cosmopolitan; *Avena sativa* is cultivated in S. continentalis. + +**Ussuri.* The genus *Ussuri* includes several species of grasses of the plantain family. The following are some of the important of the cultivated ones: *Trifolium uliginosum* (common Wheat), *Zygophyllum* (plowman's clover), *Paspalum* (spikelet, durra), etc.; *Scallops* (cereals), *Cynodon dactylon* (Sod-grass), *Cynodon nlemmii* (Sod-grass), *Cynodon ciliaris* (Jerseymeadow, ornamental, sedentary); *Medicago* (Pomace-millet); *Durra* (*Tukshir*) (Medica), or Gula; *Sorghum* (Sorghum); *Munroa* (Grain-grass); *Cynodon dactylon* (Sod-grass); *Oat-grain* (Oat-grain); *Timothy* (*Phleum pratense*)—For-tail—(*Aegilops curvipes*)—Cook's Fock (*Decalepis gracilis*)—Dog's tail (*Cosmos eriostachys*)—Giant's Fock (*Cosmos giganteus*)—Fool's Fock (*Heliotus lanatus and melo*)—Qualing-grass (*Draba nivalis*)—species of Meadow- +grass (*Poet.*; *Eremurus* [Eremurus] and *Armeria*)—several cultivatable species of Grasses are used as fodder; the seeds of many of them are used for food; the seeds being transformed to sugar ("beef from "Malta," "the gummed Dietry" etc.), and the leaves are used for medicine specially medicate before flowering; the Sugar-cane, *Saccharum secalinum*, etc. + +**Ornamental.** The richness of Trifolium, Oat-grain, Durra, flower of Durley, and the several other species mentioned above. + +The seeds of Lolium species are considered **pelletierian.** The stems of many species (including our common Wheat) are used in the manufacture of paper; they are also used for making flour in India and China; in Africa, and the sheathing-leaves of the 2-spikes of Malice. Sand-Lyme-grass (*Ely- +mor serratae*, and especially Pomace-millet are important—but for Grasses +specific use is not known). The seeds of many species are used for food; +the seeds of many species are used for medicine specially medicate before +flowering; the Sugar-cane, Saccharum secalinum, + +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +**ORNAMENTAL PLANTS.** The following are some of the most valuable of Ornamental ornamental: *Andropogon species have emmited oils ("Citronella oil")— +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** +** + +A page from a book showing text on a white background. + +**SPADICIFLORAE.** 207 + +**Family 3. Spadiciflorae.** + +The primitive form resembles that of the preceding family. In it we find the typical, perfectly developed, Monocotyledonous flower, sometimes even with free carpels and with a dry or some- what pulpy pericarp (Fig. 268), but the perianth is petaloid perianth; and this passes over into very differ- ent forms by the suppres- sion of the free-laden leaves, which are either persistent and sporophylls (unisexual flowers are common), and by the close aggregation of the flowers in a head-like cluster. The flower is **hypogynous** in every case. The inflores- cence may be either single or branched, and has often a thick and flimsy axis (a *spadix*). In Palms and Araceae it is en- veloped, at any rate partially, by a sheath or spathe, which may be petaloid (Figs. 257, 251). + +The fruit is most frequently fleshy (*berry, drupe*) or a *nut*, never a *capsule*. The embryo is small, with large, fleshy endosperm (Fig. 299 C); very rarely the endosperm is wanting. + +The plants belonging to this family are large, herbaceous or tree-like, and the leaves seldom have parallel veins. Monocotyledonous form, i.e. linear with parallel venation, but most fre- quently have pinnate or palmate leaves. + +**Order 1. Palmae** (Palms), the majority are trees with an **spadix**, cylindrical stem, having short internodes. + +A section of the stem of *Aloes juniperus* with persistent leaf-bases. +**Fig. 298.—A section of the stem of *Aloes juniperus* with persistent leaf-bases.** + +208 +**MONOCOTYLEDONAE.** + +and covered with leaf-scars or the bases of the leaf-stalks (Fig. +206), and at the summit a rosette of large leaves closely packed together (Fig. 205). An exception to this is found in *Calamovilfa* (Cunio, Rotang, *Cynodon*), a thin, creeping, herbaceous plant, which has long internodes sparsely branched, and is, e.g., the African Dom-palm (Hyphene). Notwithstanding their often enormous stems the Palms have fibrous roots, like the bulks of Monocotyledons. The leaves are usually pinnate (Fig. 207) or palmate (Fig. 208), e.g., *Caryota* *palma*, Fig. 205), and often very large; they have a well-developed petiole with an amplexicaul sheath, which is often more or less separated into a large number of fibres. In the bud the blade is entire but folded; in the leaf the expanded blade is foliate or ternate, although in some species it is palmate (thua *A A A A*, e.g., *Cocos, Chamaerops, Calamus*). The inflorescence is simple, terminal when in Sago-palms (Me- +crocycas), or lateral when in *Palmae* (Osmunda); in the ter- +minal, the plant is monocarpic, and dies after flowering; it is often a very large and branched panicle with numerous flowers either borne externally or embedded in it, and enclosed either in one sheath or in several sheaths (Fig. 209). In the latter case one for each branch. The flowers are sessile or even embedded, regular, generally *unisexual* (monocious or dioecious) with the usual diagram (Fig. 275): the perianth is in- +comparable with that of other plants; it is either short and fleshy or flimsy; 3, rarely 3 or many stamens. The 3 carpels remain either distinct or form one, generally 3-locular, ovary. The style is short. There is one ovule in each carpel. Often during ripening 3 carpels become sterile and fall off; sometimes only 2 fertile +drops or nut, generally one-seeded, with a large horny or horny endosperm with hard thick-walled cells (e.g., Date-palm). In some (e.g. Coconut) it is thin-walled, soft, and oily; in several +*runicinate.* + +When germination commences in the Cocoonat, date, etc., the apex of the cotyledon remains in the seed and develops into a strong wall to withdraw the endosperm; in the Cocoonat it attains a considerable size (Fig. 209 C) and + +1 [Although antheridial stems are characteristic of the Palms, yet brachoid sporiferae are recorded from some eleven genera. The branches are developed from them.] The stem is usually unbranched except when a monopodial bulb has been developed. A few Palms develop axillary branches at the base of the stem; these form rhizomes, and give rise to clusters of aerial stems.] + +A diagram showing the structure of a Palm flower. + +SPADICIFLORE. 299 + +assumes the form of the fruit. The endocarp in the Coconut is hollow and the interior is filled with "milk." In the Date-palm and the Vegetable-ivy (Phytolacca) the cell-walls of the hard endocarp serve as reserve material. + +1. **Phoenix**. *Phoenix* (Date-palm) has pinnate leaves with channelled leaflets and dioecious flowers with 3 free carpels, of + +A close-up of a Phoenix palm leaf. +Fig. 297.--Indusium +covering one of a Poinciana flower. +At the top $f'$, at the base $b$, +the groove. + +2. **Saralee**. These have fan-like leaves with channelled seg- + +which usually only one develops into a berry with membranous endocarp ; the large seed has a deep furrow on the inner side, and horny endosperm. + +A close-up of a Saralee plant showing its fan-like leaves and seed. +Fig. 298.--Liriodendron endocarpum. + +300 +MONOCOTYLEDONAE. + +ments; flowers 5 or polygonous, rarely dioecious, with 3 separate or only slightly united carpels, all of which are sometimes developed into fruits (berry or drupe, with thin stone).—Chamaerops, the palm-like tree of the Mediterranean region; Cephalocaryum, the palm-like tree of the tropical East Indies; Cynara, the artichoke; Cynara scolymus, the Jerusalem artichoke; Cyrtomium, the fern-like plant of the Himalayas; Dicranopteris, the fern-like plant of the Himalayas; Dioscorea, the yam; Euphorbia, the spurge; Ficus, the fig; Ficus carica, the common fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacred fig; Ficus religiosa, the sacredfig + +**SPADICIFOLIUM.** 301 + +abundance of oil. *Cocos* (the Coconut-palm), *Attales*, *Elaeis*, *Acrocomia*, *Bactris*. + +**4. LEUQUOTYCTUS.** The floral-leaves and flowers are borne in 2 rows on the spadix. The spadix is covered with a membranous ovary, which is coated by a layer of hard, shining, imbricate scales. The majority of the species are thorny, and climb by means of the thorny leaves. Some have fan-like (*Mancilla*), others pinnate leaves (*Zygphes*, *Calamus*, *Eugeniaea*, *Metaxylon*; the stem of the latter after the first flowering). + +**5. Euphorbia.* Large Fan-palm without thorns, but 3-lobular ovary, droops with squarish stipules, and has a very large number of many stamens; *Hypheze; Borneus (Palmyra-palm)*. + +**6. Acrocomia.* A large fan-palm group, featuring Palms, Beryx, *Arauca*, *Entophyllum*, *Orobanche*, Chondrodendron, Gomphrena, Gnetum with bi-pinnate leaves. + +**7. Pterocaryon.* Flowers with rudimentary perianth united into close clusters; *Phyllodiscus* (Vegetable-nipa). + +Durrerionum. About 1100 species are known. In Europe only the Dwarf-palm (*Chamaerops humilis*) and the Fan-palm (*Phoenix dactylifera*) belong to North Africa and West Asia. Other African genera are Hypheze (Downpalm) and Elaeis (E. guineensis, Oil-palm). A large number of species are found in South America and in the East Indies. The following are American—*Manicaria*, *Acrocomia*, *Attales*, *Chamaerops*, *Oreodoxa*, *Euphorbia*, *Atteles*. *Antarcite*—*Metaxylon*, Calamus, Areca, *Jussiaea*. The following are Asiatic—*Bactris*, *Corypha*, *Cycas*, *Cuscuta*. Some have no relation to any other genus; some are found on the coral islands of the Pacific Ocean, and is also the only one which is capable of both hemi- +spheres. + +*Areca*. Palm belongs to the most useful plants; they contain many valuable oils and are used in medicine. The hard timber being adapted for many purposes on account of the light weight and strength of its wood. The palm is cultivated in India in the form of Calamus-calamus (from India). Saba is obtained from the pith of Metaxylon ramonii (Sapindaceae, Sumac-trees), Mancilla flexuosa, etc. +Sugarcane is obtained from Saccharum officinarum (Gramineae); *Pentas* +*cinerea* and *ferruginea*, Borneus falcifolius (Attales Palmyra-palm), Areca +sanchezii, etc., by cutting off the young leaves at the base of the plant. For the manufacture of mats and brushes, etc., are obtained from the outer cover- +ing membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from the inner covering membrane of the coconut (Araceae); also from +the young beds of many species, especially Euterpe, Cocos, Attales, +etc., are used as "cabbage." Palm-oil is obtained from this oily mesocarp + +302 +MOROCCOPEDILEGONI. + +of the plum-like fruits of *Elaeis guineensis* (W. Africa), and from the seeds, +when it is largely used in the manufacture of soap. *Eremal* Eremus from the Latin eremus, desert, is applied to this genus, because the leaves are on the endocarpus (Cocos maculata). The seeds and the unique fruits of the Arona palm (*Aronia arctica*) are chewed with the leaves of the *Isolat- +pers* persimmon (Persimmon persimmon) by the natives of the island of *Fijiophleps macrocarpa* (S. America). Many species are cultivated in the tropics as ornamental plants, but in this country only *Caryota umbraculifera*, *Liriodendron tulipifera*, and *Caryota mitis* are grown. Of these, the last two just mentioned, many others are of importance, but these are much the most useful. + +Order 3. Cyclanthaceae. This is a small order related to the Palms (14 +species from Tropical America), with flat-leafed, folded leaves. The flowers are tubular, with a long tube and a broad base; the ovary is sessile. *Cyclamen* +Ovary unilocular, ovules numerous. To this belong *Cordyline patens*, whose leaves are used for Panama hats. + +Order 4. Araceae. This is another small order, forming a transition to the Araceae. The woody, (apparently) dichotomous stem is supported by a large number of aerial roots, which sometimes entirely support it when it is young. The leaves are usually pinnate, and are crowded together, and arranged on the branches in three rows, which are often obliquely displaced, with the formation of three spiral lines; they are, as in the Bromeliads, attached to a sheath. The flowers are small and green, pro- +vided with thorns. The *q-flowers* are borne in branched, the *p* un- +branched spadices; the *r-flower* is solitary in each leaf-sheath, but have no flower below. Veratrum alpinum. The drupes or fruits unite into a globular fruit—Albus about 80 species in the islands of the Indian Ocean.—*Fennel*, *Frigiliana*.—*Corms perhaps in the park of the Hau. + +Order 5. Typhaceae. The flowers are unisexual, monocious, +and borne in cymose or cyathia; or in a tubular capitulum; or +in inflorescences above the *q-beak*. The perianth consists of a +definite number of scales (*Spermatocarpus*), or in its place numerous irregularly-ranged hairs are found (*Typhae*); in the *g-flower* there are two or more petals; in the *h-flower* there are 1-2 +carpels with a prolonged stalk; or 1 pendulous ovule. The stamens are furnished with a seed-cover, which is cast off on germination. +The few species (about 20) which belong to this order are marsh plants growing in rhizomes (and hence grow in clusters); the leaves on the aerial shoots are borne in two rows, narrow, very long and linear. +*Spermatocarpus* (Bar-red). The flowers are borne in globose capitula or cyathia; or in a tubular capitulum; or in small +scaloce; pistil bi-carpellate. Drype, dry and woody. The stalk of the lower *v* capitula is sometimes united with the main axis, and consequently the capitula are situated high above their subtending-lea. + +A stylized illustration of a plant with elongated leaves arranged in three rows. + +**SAPIDELOIDEAE.** + +Typha (Bulrush, Reed-mace) has a long, cylindrical, brown spike, the lower portion bearing 3-5 flowers, and the upper 5-flowered, which is divided into joint by alternate leaves. The 5-flowers have 1 carpel. The perianth is wanting, represented by a number of fine, irregularly-placed hairs; pistil unicarpellate. Fruit a nut. + +To this genus belong the Typhoideae, in which both generic nature species are found. The pollination is effected by the wind, and consequently the anthers project considerably, and the stigma is large and hairy. The flowers are white or yellowish-white; the leaves are long, fine lains surrounding the nut of Typha assist in its distribution by the wind. + +Fossil Typha in the Tertiary. + +Order 5. **Araceae (Arums).** The flowers are small, and always borne on a short stem, or peduncle on an umbel, often very feebly spiked, which is enclosed by a spathe, often petaloid and coloured (Fig. 301). The fruit is a berry. Outer integument of the seed fleshy.—The leaves have generally sheath, stalk, and blade with distinct margin; but in some cases they are entire (Fig. 302), or dentate (Fig. 302), seldom long with parallel venation as in the other Monocotyledons (Acorus, Fig. 300). The Araceae are quite glabrous, generally perennials having with tubers or rhizomes. Many have been cultivated for ornamental purposes; but few are useful; for example, while some have a perianth, in others it is wanting; in some the perianth-leaves are free, in others united; some have hermaphrodite flowers, but the majority unisexual (monocious); some are monoecious (dioecious), others dioecious. Some have orthotropicous, anaporeous, or campyloptorous, erect or pendulous; the ovary is 1-many-locular; some have seeds with endosperm, others without. In fertile there are great differences. While some, e.g., Coto- +dendron (Rice), have many-seeded fruits with a large embryo, most of the rest woody, others are climbers, epiphytic, and maintain themselves firmly by means of adventitious roots, on the stems and branches of trees, or even on steep rocks. +On Phalaris (Phalaris), the leaves are all alike (Fig. 303), but various branched forms appear: the pedate leaves of Helicobolus (Fig. 303), etc., are cycad-like; the leaves of the primitive dicotyledons, profusely branched as would be expected (the vascular bundle being in one plane), but grow faster than those between them; among these latter to be torn, and their leaves to be shed at maturity. In some plants the leaves are persistent; the presence or absence of laterals, rachises, reseass-pieces, groups of mullage-les should be noted. Engler makes use of these anatomical peculiarities for a classification. + +**A. ONONIETE.** *Calamus-group.* q., hypogynous flowers of a completely formed monocotyledonous type (number in the whorls 2, 3, or 4)—*Acorus* (*A. calamus*, Sweet-flag) has a regular, + +w. n. + +Acorus calamus plant. + +304 + +**MONOCOTYLEDONES** + +3-merons, pentacyclic flower (Fig. 300 C, D). They are marsh-plants, with creeping rhizome, triangular stem, and terminal panicle (Fig. 300 A); the inflorescence is terminal, appa- +rently lateral, being pushed to the side by a long, sword-like spathe (Fig. 300 B) **Lathyrus** (Præ +2, A3 +2, G2g Fuchsi): Oenothera (unilocular corolla with one ovary), etc. + +A plant with a long, sword-like spathe. +A plant with a long, sword-like spathe. +A plant with a long, sword-like spathe. + +Fig. 300.—*Acorus calamus*. A habit (much reduced); B × 15; C × 15; lower D diagram; E longitudinal section of an ovary; F an ovule. + +A plant with a long, sword-like spathe. +A plant with a long, sword-like spathe. +A plant with a long, sword-like spathe. + +Fig. 301.—*Avena sativa*. The spathe (A) in B is longitudinally divided. + +SPANDICIFLOR. +305 + +B. CALLER. Flowers hypogynous, naked; $f$ — Calle (C. palustris). All flowers in the spike are fertile, or the upper ones are $f$; 6–9 stamens; ovary unilocular with many basal ovalets. Marsh-plants with creeping rhizome and cordate leaves.—Monotera, Rhaphidophora, etc. + +C. Calla. Flowers monoecious, naked, $f$-flowers on the upper, $g$ on the lower part of the spadix.—Arum (Fig. 301). The spadix terminates in a naked, club-like portion ($k$); below this is a number of sessile bodies (rudimentary flowers), with broad bases + +and prolonged, pointed tips ($b$); underneath these are the $g$-flowers ($m$), each consisting only of 3–4 short stamens, which are reniform and sterile; between them follow, last of all, $q$-flowers ($j$), each of which consists of one unilocular ovary, with several ovalets. Perennial herbs, tuberous, with cordate leaves.—Droseraceae; Bistem; Arianum; Piso-lia (Atherusa) ter- minata (Fig. 302). + +$g$, 3–4 stamens; $q$ with 3 stamens, 1–5-locular ovary (S. Africana).—In some genera sterile flowers are present between the $f$ and $g$ portions of the spadix (e.g., Arum); in others they are absent. In the latter case the base of the spadix divides the cavity of the spathe into two chambers, the anterior + +A diagram showing the structure of a spadix with different parts labeled: $f$, $g$, $q$, and $b$. The diagram also shows the position of the spadix within a spathe. +Fig. 301.—Calceolus, Boryi. + +306 + +MONOCOTYLEDONS. + +containing one $y$, and the posterior 2-4 to 5-flowered in two series; in some the stamens in the single $y$-flowers unite and form a columnar "synandrium" (e.g. in *Jacaranda*, *Coccoloba*, *Aesculus*, *Calodendrum*, *Taxodium*, "Pseudognomus", a remarkable species of *Corylus*), while in others they are separate, on one side, with the stamens, and the flowers are arranged upon it in rows, the $y$ to the outside, and the $x$ in the middle (Zantera has a similar case).—Plants entirely herbaceous, but some of them, e.g. *Corylus* and *Corylus* var. *heterophylla*, have erect racemes of leaves; in it also the stamens and anthers are united; at the base of $y$-flower is borne, which consists of one uniseriate ovary, and above several $y$-flowers, a short peduncle. + +Bionotus. The inflorescences are adapted for self-pollination; they are prophyllous, since the leaves, almost entire, elongate come to maturity and either before or after flowering. In some species, such as *Bionotus* and *Lysimachia*, some pollinators themselves fly by the pollen from the higher $y$-flowers falling into the lower ones. In other cases, the pollen is deposited on the stigma by means of pollination effected by animals. The coloured spathe and the naked end of the spadix (often coloured) of certain genera form an excellent perchament in other circumstances. The spadix of *Eichhornia* is covered with long hairs; *Macropis* is worthy of notice; small flies and midges creep down into the spathe, between the sterile flowers (Fig. 281), in which are situated where the spadix is placed, and deposit their eggs on the stigmas; these receive the insects; in the meantime, the stigmas are in a condition to receive any pollen they may have brought with them; after pollination the stigmas wither, and the fruit ripens. In some cases, this is followed by a second improvement; after this the nectar ($x$) is opened and after its pollen, the sterile flowers wither. In other cases, spadices, and enter and pollinate other insectivorous ones.—In many, a rise of temperature causes a change of place taken during flowering: a spadix may be raised as much as 30° C., above the temperature of its surroundings. In some cases, when water is scarce, many species absorb such large quantities of water by their roots that water is forced out in drops from the tip of the leaf; this may often be observed in *Eichhornia*. + +About 500 species in 100 genera. Hence, the Tropeae, especially S. America, India, and the Indian Islands, probably in shady, damp forests growing on epiphytes. In Europe only about 10 species are known; very few are found. *Anthericum* was introduced into Europe from Asia about 500 years ago; however, never seen any fruit as the pollen is sterile. In England only one species is found: *Anthericum ramosum*. In North America are the only native species. *Coccoloba* natans comes from Polynesia and the Indian Islands, and also *Aesculus macrantha*. Fruits in Cretaceous and Tertiary. + +Uses. Many species have pungent, and even poisonous properties (e.g. *Daphne*, *Euphorbia*, *Rhamnus*, etc.), but many are used for roasting; the rhizomes of many species of *Celosia* (Coccoloba: C. emarginata; *Cedrela*: etc.) are very rich in starch, and in the Tropeae form an important source of food for man. The seeds of many species contain albumen or albumen-like substance; this contains albumen or albumin and scirin which are used in perfumery. Many are ornamental plants, e.g. *Zantedeschia aethiopica* (South). + +SPADICIFLORE. +307 + +Africa), generally known as "Galla," and Monsters delicata ; many other species are grown in greenhouses. + +Order 6. LEMNACEAE (Duck-weeds). These are the most reduced form of the Spadiciflora. They are very small, free-swimming water-plants. The vegetative system resembles a small, flat-leafed plant, with a long, slender stem, from which arise several short branches, this branches by producing a new, similar leaf-like body, which springs from a pocket-like hollow (indicated by a dotted line in the figure) on each side of the older one, at its base (or only on one side). The branching is irregular and helical (fig. 305, d, where $A$, $B$, $C$, $D$ represent the first, 2nd, 3rd, and 4th leaves respectively). The leaf-like bodies are, according to Hopplauer, leaf-like stems, and thus Lemna + +A diagram showing the structure of a duckweed plant. +Fig. 305.--Lemna. A reproductive system; $A$, portion of a plant with flowers; one stamens and half of the carpel projected; the remaining portions being indicated by the dotted line. +has no other leaves than the spathe and the apericolla; according to the investigations of Engler they are stems whose upper portion (above the "pocket") is leaf-like. The lower part is represented by a single leaf-like petiole. The inflorescence is a very much reduced Araceae-spadix, consisting in Lemna of 1 or 2 stamens of unusual length (1-stamens $2$-flower), 1 unilocular cavity (for the pollen), and 1 or 2 perianth-leaves (for the nectar); in Spirodela polyrhiza, etc., whose daughter-shoots begin in addition with 1 basal-leaf. Engler has given a detailed account of these plants in his "Flora" (Engler). On the germination of the seed a bud of the spathe is thrown off as a lid, so that an exit is opened for the radicle.--19 species. In classificatory order: Lemnaceae; Tropaeolaceae; Hydrocharitaceae; Lemna minor, trialesis, etc.; Spirodela polyrhiza, and Ptilota arachnoïdes, the smallest Flowering-plant. + +The following species are cultivated in England: + +**Lemna minor** (Linn.) Schult. & Schult.f. (fig. 305). + +**Lemna trialesis** Linn. (fig. 305). + +**Spirodela polyrhiza** Linn. (fig. 305). + +**Ptilota arachnoïdes** Linn. (fig. 305). + +368 + +**Monocotyledons.** + +**Family 4. Enantioblastes.** + +The flowers in this family are agynoecious and have in part the general monocotyledonous type with 3 trimerous whorls completely developed in one plane, but the third whorl fewer, and in part the flowers so much reduced that the type is very difficult to trace. +On the one hand the family is well developed and has capitose inflorescences (Bromelaceae), on the other hand it is distinctly reduced (Cyperaceae). This fact is explained by the difference from the fact that the ovule is not, as in the Liliiflorae and nearly all other Monocotyledons, matrotous, but orthotrous, so that the embryo (Bhara) becomes placed at the end of the scale opposite (anterior) to the stamens. The flowers of the plants which belong to this family are by certain authors grouped with the Bromeliaceae and Panderoideae, etc., into one family, *Eranose*, so named on account of the mealy endosperm, the distinguishing characteristic of the Eriiflorae then being thus the endosperm of mealy and horny. + +Order 1. Commelinaceae. The complete Liliiflorae structure without great reductions in the number of whorls, but with generally few ovals in each series of whorls, is found in the Commelinaceae. The flowers are mostly perigynous with 3 or 5 stamens, some of which are included into our organs and greenhouses. The stamens are nodules; the leaves often *clap- sag*; they are usually deciduous; the petals are wanting; the sepals form a large series falling in the median line of the bracts, and after flowering they bend regularly to the right or left, upwards or downwards. They are more or less cupped, and their margins are often ciliate. The perianth is of different forms or partially suppressed. The outer series of the perianth is epicalyx, the inner petaloid, generally visible or blue; the filaments are sometimes shorter than the petals; they are often united into a tube (as in showing protandrous movement). Each a trilocular capsule with bicornidal deliquescent (generally free-seeded) in some cases. The rudicle is covered by an external sheath. The seeds are small and compressed. The abundant rudicles are by elongated cells whose transverse walls they perforate. Capsule generally dehiscent. + +Order 2. Mayacaceae. This order is closely allied to the Commelinaceae. +7 species. American marsh- or water-plants. + +In most of these plants, as in this family, the flowers are united into compound inflorescences, with which an accompanying reduction in the flower. +Order 3. Kyrtidaceae (50 species). Marsh-plants with radical, often equi- +nail leaves, and with a single flower on each leaf. + +The flowers, as in the Commelinaceae, have sepals (which however are more chaffy and petal), but the outer series of stamina is wanting. Capsule (generally) mucronulate. + +Order 4. Rapateaceae. Marsh-plants with radical leaves, usually in two + +LILIIFLORE. +309 + +roose, and several spikes on the summit of the main axis, clustered into a capitulum or unifoliate flower. Each spikelet has numerous imbricate floral- +leaves and one flower. 24 species. South America. + +United States. The genus is allied to *Monocleptes*, a tropical order. The flowers are borne in a capitulum surrounded by an involucre, very similar to that of the Compositae. The flowers are very small, unicellular, 5-6 mm. long, with a tubular corolla. The leaves are linear-petiolate; the leaves of the inner perimeters are often scabrous and more membranous than the outer; in some the outer series of stamens are suppurated, and the inner ones are sterile. The receptacle is conical. The leaves are generally radical and glaucous—25s species; *Ericaceae*, *Fagaceae*, etc., e.g. *Aegopodium* on the west coast of Scotland, and Ireland, and in North America. + +Order 6. **Resentaceae**. A small, especially S. African and S. Australian, arborescent or shrub-like family, with 2-3 orders, viz., *Euphorbiaceae* (the Juncaceae and Cyperaceae). The leaves are often reduced to stipules. The flowers are dioecious, the perianth as in *Juncus*, but the outer series of stamens expresses a calyx-like structure; the corolla, however, may be unilocular, and the fruit a nut. *Ericaceo.*, etc. + +Order 7. **Crepidiaceae**. These are the most reduced plants in the family; they have a rudimentary stem, and their leaves are very small, naked. Stamen 1-2; carpel 1—2—3—5 cells. Australia—*Gnaphalium* (Rosaceae generally 5 with 1 stamen and 2—3 carpels). + +Family 5. **Liliiflorae**. + +The flower is constructed on the general monocotyledonous type, with 5 alternating, 3-membranous whorls (Fig. 278) by the suppression of the inner whorl of stamens; in a few the position in relation to the bract differs from that shown in Fig. 278; in some cases the leaves of the trimerous, di-or tetramernous flowers are found (e.g. *Majestanthemum*, *Paris*). Flowers generally regular, hermaphrodite, with simple, +petaloid, coloured perianth (except, for example, *Bromeliaceae*); ovary trichogynous, generally; or with a number of ovules in the inner whorl (Fig. 304 C, D). Endostele—veins present—a very natural family, of which some divisions in part overlap each other. The habit varies; the leaves are however long, entire, with parallel venation; except in Dioscoreaceae (Fig. 313). + +In the first orders of this family the flowers are hypogynous, and in the first of these orders (Liliiflorae) there is no calyx at all; in the following the flowers are epigynous and in some reduced in number or uni- +carnate ; axinum with lobularis deltoidea, or a berry. + +Hymenocreae: *Chlorophyllum*, *Lilium*, *Convallariae*, *Bromeliaceae* (in part). + +A diagram showing the construction of a flower according to Liliiflorae. + +310 +30000COTYLEDONES. +Erythroxylus flowers: Amygdaloidae, Iridaceae, Bumeliaceae (in part), Dios- +cureae. + +Order 1. *Colchicaceae*. The flower (Fig. 304.4) is 2-regular, +zygomorphic, trimerous in all five whorls (6 stamens); anthers usually extrorse. Gynoecium with 3 free styles (A, B, D); fruit a capsular or follicular capsule, rarely a berry. The underground stem is generally a corm or rhizome, seldom a bulb. + +A. *Veatearum—Veratrum*: perennial herb, stem tall with long internodes and broad, folded leaves; the flowers andro- +monous, zygomorphic, 5-parted, with 3-lobed leaves (Fig. 304.5), and globular anthers; inflorescence a panicle. *Zygadenus*. +B. *Toileffera—Nerium*: and *Tofieldia* have leaves alter- +nate (unifoliate), the stem short or long, the leaves borne in corylettes; +racemes or spires. *Nerium* forms an exception to the order by having a simple style and fruit with bilocular dehisence; + +A diagram showing the structure of a flower. +Fig. 304.—*Toileffera*: A flower; B stamen; C trimerous section of ovary; D gynoecium, with one style; E ovary; F fruit after dehiscence; G longitudinal section of a seed. + +*Tofieldia* by the introrse anthers. In this they are related to the Liliaceae. Nerium has peonaceous properties, like many other Colchicaceae. + +C. *Cochlearis—Codonopsis* (Autumn Crowea): perennial herb, with a long, funnel-shaped, papilionaceous perianth, and introrse anthers. The flowers of *C. umbellata* spring up immediately from the underground stem, which forms a corm or a bulb formed of one internode. Generally the flowers in one leaf-spike begin to spring the raised foliage-leaves appear simultaneously with the fruit. The flower is protogynous, and is prolonged by its stamens (fimbriate-basal, etc.) which seek the inner side of the perianth tube when the stamens are on the tube. The length of the tube produces the fruit, and not, as in other cases, the middle part of the perianth. *Cochlearis* have uniplicate perianth leaves, free, but closing together like a tube. +125 species; chiefly in North America and South Africa. *Tofieldia* is an + +LILIIFLORE. +311 + +Arctic plant. The order is rich in pungent, poisonous alkaloids (venin, colchicin, etc.), *Oxyporus*, the seeds of *Colchicum autumnale* (Europe) and *Colchicum bulbocodium* (Mediterranean), and the thyrshiums of *Ferula* *alba* (mountains of Central Europe). + +Order 2. Liliaceae (Lilies). Flowers as in the Colchicaceae but with introrse anthers; ovary free, 3-locular, with single style; capsule 3-locular with loculocidal dehiscence.—The majority are + +A diagram showing the structure of a flower and its roots. +Fig. 365.—Colchicum autumnale. A Corm seen from the front: $y$ stem, $e'$ scale-leaves enclosing the flower-stalk; $w$ base of flower-stalk with roots ($v$). B Longitudinal section of root showing the three roots ($u$, $v$, $w$); $a$ shoot; $b$ bud; $c$ young leaf; $d$ mature leaf; $e$ axis of the plant; at flowers and leafstalks of previous year, the swollen head portion forming the receptacle; $f$ stamens; $g$ pistil. C Longitudinal section of root showing the three roots ($u$, $v$, $w$) and has the following parts: the base bearing the roots ($v$), the central year ($u$) which becomes the stem in the next year, the axis bearing the anthers ($f$, $g$), the stipules ($a$, $b$, $c$), and the flowers ($d$, $f$) which are borne in the axils of the opposite stipule leaves. + +311 + +312 +MONOCOTYLEDONES. + +herbs with bulbs; the inflorescence is terminal. In many species reproduc- +tion takes place by means of bulbs (small bulbs) formed in the axils of the +leaves (e.g.: *Lilium bulbiferum*, *Festuca* *lutea*, etc.), or by means of +bulbs produced in the axils of the leaves (e.g.: *Lilium bulbiferum*). In some +species several buds are developed as bulbs in the axils of the bulb-seakers them- +selves (anomalous bulb-seeks close together), and in some the formation of +bulbs occurs in the leaves. + +A. TULIP, TULIP GROUP. Bulbs. The aerial, elongated stem bears the foliage-leaves. Flowers few but generally large, with +few perianth-leaves. Tulips; style absent, no honey; flowers generally regular, sometimes irregular; corolla hypogynous, with +round or oblong perianth at the base of each segment; *Lilium*; +*Lilium* perianth widely open, generally turned back with a +covered nectary-groove in the base of each segment. Anthers +versatile. + +B. HYACINTH, HYACINTH GROUP. Bulbs. Leaves radical; aerial +stem leafless with raceme or spikus. In some the perianth-segments are free, in others united. Honey is produced often in glands or in the nectar-grooves (nearly always); *Hyacinthus* has a +unifol stem; *Sulla*; *Sulla* has a tuft of flower-leaves below the raceme; *Agrimonia*; *Hyacinthus*; *Pachysandra*; *Chionodoxa*; *Muscaria*; +*Vulcanica*; *Uvularia* + +C. ALEUR, OXON GROUP. Generally bulbils. Leaves radical. +Stem bearing a compound umbellule or capitate inflorescence +of unifolied helical cymes, which before flowering are sur- +rounded by two broad involucral bracts—*Helianthus*. Filaments often +paler on one side than on the other. +Some species have flat leaves: e.g., *aestivum*, *Garcia*, *a. porum*, *Leck*: d. +uniserial; others have round, hollow leaves: e.g., *a. cupa*, *a. filiformis*, Winter Oats: *Oxalis*. Some have long, narrow leaves: e.g., *Chion*: *Gagea*; +honey is secreted at the base of the perianth, no special nectary; +inflorescence few-flowered—*Amapasana*: *Telatela* + +D. ANTHURIUM: Rhizome; no leaves but fresh and thick— +anthurioid: *Anthurium*, *Alocasia*, *Araceae*. Bulbils have an almost leat- +less stem with curling, climbing branches. +E. AGAVE, Agave. Stem generally aerial and tree-like, bearing on its sum- +mit a head of flowers surrounded by a sheath of leaves—*Agave*: 2-leafed or +unbranched—*A. amara*: *Asteria*: 2-leafed secondary thickening—p. 276 + +F. HETERODENDRON: Phlomis. New Zealand Flax: *Phacelia* +(Fig.)—(Fig.) + +At this point the following are best placed: *Aphelandra*: (*a.* multiplicata); +*Xanthorrhoea* ([Blankeney]: *Xerota*: Lomatiumina): Kinaea: the very membranous, +dry perianth segments resemble that of the Fucinaceae, and also there are only +1-leaf ovules in the leaves. + +LILIIFLORE. +313 + +Pollination by insects. Honey in some is produced on the perianth (see Tulipes), in others by glands on the corolla (in the septa and parietal placentas, epiphyllum, gladiolus, etc.), or by the nectariferous stamens (in the orchids, Hemerocallis, etc.). Some *Sitan*-species are pretentious. *Pretiaria* is visited by bees. *Lilium martagon* by moths, *L. belliforme* by butterflies, *Phormium* (New Zealand) by honey-birds. + +A plant with a tall, narrow, upright stem and a large, flat, greenish-yellow flower spike at the top. +Fig. 891.--Aloe. + +About 1,500 species; rare in cold climates; their home is in sunny plains with firm, hard soil, and warm or mild climate, particularly in the Old World (i. Africa). The flowers are usually solitary, but sometimes two or three among the flowers appear in great profusion, and after the course of a few weeks disappear; during the hot season their life lies dormant in the bulb, hidden underground. + +314 +MONOCOTYLEDONES. + +The woody species are tropical—The majority of the introduced Lilaceae (Peristylia imperialis, Imperial-orchid; Lilium canadense, Tulip-persian; *Eupatorium* purpureum, Purple-stemmed aster; *Lilium* regale, Regal-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lily; *Lilium* tibetanum, Tibet-lily; *Lilium* aureum, Golden-lily; *Lilium* taliense, Tali-lily; *Lilium* aureum, Golden-lilly) are natives of the Himalayas and the East Indies. The Euphorbiaceae (Euphorbia cyparissias), the Euphorbiae Steppes ; A. exotica from Persia (?); A. exotica is not known well according to the author. The same applies to the genus of A. exotica ; A. exotica is not known well according to the author. The same applies to the genus of A. exotica ; A. exotica is not known well according to the author. +Many bulbs have pungent properties: many onions are used as culinary plants. +The best-known bulbous plant is the tulip (Tulipa). The flowers of some species of Daisies are obtained from the stem of Spathularia hirsuta and auriculae Auriculae ; "Auricula," the dried root of S. African species of daisies (S. africanus) (the bulb known as "Scilla" from Uragina (Scilla) scillifera (Mediterranean). + +Order 3. Violariaceae. This order differs from the Lilaceae in having the fruit a berry (Fig. 308) and in never being bulbous ; the seeds are less numerous. + +A. Genus Violaria. The valley-Gallory Group. Rhizome (Fig. 307) and normal foliage-leaves—Polygalastris : rhizome creeping; +a b c d + +Fig. 307.—Eunicea of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. + +A. Genus Violaria. The valley-Gallory Group. Rhizome (Fig. 307) and normal foliage-leaves—Polygalastris : rhizome creeping; +a b c d + +Fig. 307.—Eunicea of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. + +A. Genus Violaria. The valley-Gallory Group. Rhizome (Fig. 307) and normal foliage-leaves—Polygalastris : rhizome creeping; +a b c d + +Fig. 307.—Eunicea of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. + +A. Genus Violaria. The valley-Gallory Group. Rhizome (Fig. 307) and normal foliage-leaves—Polygalastris : rhizome creeping; +a b c d + +Fig. 307.—Eunicea of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. + +A. Genus Violaria. The valley-Gallory Group. Rhizome (Fig. 307) and normal foliage-leaves—Polygalastris : rhizome creeping; +a b c d + +Fig. 307.—Eunicea of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. + +A. Genus Violaria. The valley-Gallory Group. Rhizome (Fig. 307) and normal foliage-leaves—Polygalastris : rhizome creeping; +a b c d + +Fig. 307.—Eunicea of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. + +A. Genus Violaria. The valley-Gallory Group. Rhizome (Fig. 307) and normal foliage-leaves—Polygalastris : rhizome creeping; +a b c d + +Fig. 307.—Eunicea of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. + +A. Genus Violaria. The valley-Gallory Group. Rhizome (Fig. 307) and normal foliage-leaves—Polygalastris : rhizome creeping; +a b c d + +Fig. 307.—Eunicea of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. + +A. Genus Violaria. The valley-Gallory Group. Rhizome (Fig. 307) and normal foliage-leaves—Polygalastris : rhizome creeping; +a b c d + +Fig. 307.—Eunicea of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. + +A. Genus Violaria. The valley-Gallory Group. Rhizome (Fig. 307) and normal foliage-leaves—Polygalastris : rhizome creeping; +a b c d + +Fig. 307.—Eunicea of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. +Illustration of Polygalastris. + +A. Genus Violaria. The valley-Gallory Group. Rhizome (Fig. 307) and normal foliage-leaves—Polygalastris : rhizome creeping; +a b c d + +Fig. 307.—Eunicea of Polygalastris. +<水印>Polygalas

Polygalas illustration

Ageny Violaria Gallory Group

Rhizome (Fig.) and normal foliage-leaves—Polygalas : rhizome creeping;

a b c d

Polygalas illustration

Ageny Violaria Gallory Group

Rhizome (Fig.) and normal foliage-leaves—Polygalas : rhizome creeping;

a b c d

Polygalas illustration

Ageny Violaria Gallory Group

Rhizome (Fig.) and normal foliage-leaves—Polygalas : rhizome creeping;

a b c d

Polygalas illustration

Ageny Violaria Gallory Group

Rhizome (Fig.) and normal foliage-leaves—Polygalas : rhizome creeping;

a b c d

Polygalas illustration

Ageny Violaria Gallory Group

Rhizome (Fig.) and normal foliage-leaves—Polygalas : rhizome creeping;

a b c d

Polygalas illustration

Ageny Violaria Gallory Group

Rhizome (Fig.) and normal foliage-leaves—Polygalas : rhizome creeping;

a b c d

Polygalas illustration

Ageny Violaria Gallory Group

Rhizome (Fig.) and normal foliage-leaves—Polygalas : rhizome creeping;

a b c d

Polygalas illustration

Ageny Violaria Gallory Group

Rhizome (Fig.) and normal foliage-leaves—Polygalas : rhizome creeping;

a b c d

Polygalas illustration

Ageny Violaria Gallory Group

Rhizome (Fig.) and normal foliage-leaves—Polygalas : rhizome creeping;

a b c d

Polygalas illustration

Ageny Violaria Gallory Group

+ +B.
Ageny Violaria Gallory Group
Schlumberger leaves and green
narrow leaves with a terminal rhiocone.
The aerial shoots are very richly branched;
the numerous needle-like bodies upon the plant are leafless shoots which are crowded together in double scrophoid cymes in the axils of the scale-leaves;
the two first + +LILIIFLORE. +315 + +lateral axes, placed outside to the left and right, generally bear + + +A sketch of a plant with long, narrow leaves and small flowers. The leaves are green and have a slightly wavy edge. The flowers are small and clustered together at the ends of the branches. + + +Fig. 308. -Similar pseudophyllidium ; a shoot of male plant ; C d-ducer ; D berry, almost ripe ; E the same in longitudinal section. B Similar pseudophyllidium : portion of branch with base of leaf and budlet. + + +316 +MONOCOTYLEDONAE. + +**flowers.** *Polygonum* — *Roses* (Botcher's broom) is a S. European shrub with leaf-like, oval or ellipsoid leaves (phyllodiscus) which are borne in the axils of scale-like leaves, and bear flowers on the central line. Dillenia, *Dillenia indica*, has extreme *sepal* and *bracteole* bearing its flowers on the edge of the flat shoot. + +**C. SHILACEAE.** *Smilax* (*Sarsaparilla*) (Fig. 308); climbing shrubs with the leaf-shoots produced into tendrils. The levaue have 5-8 strong nerves proceeding from the base, and are reticulate. Orthotropis, *Orthotropis* (Dyer's green wood), is a S. American shrub (Fig. 307). + +**D. DULCERAE.** Fruit in some a berry, in others a capsule. The stem of *Dracaena*, when old, has the appearance of being dichotomously branched; it has the power of increase in thickness, and may become enormously thick. The *Pomaceae*, with their large seeds, are very common in the tropics. The *Acanthus*, with its large leaves, is a S. American plant (Fig. 309). The *Lilium*, with a height of 14 m., or the leaves are large, linear or lanceolate—Gentiana (genia), various species in gardens and greenhouses (Tussie in Italy chiefly all); the *Lilium* is a S. American plant. + +**FOLIATION.** *Ficus carica* and *Convolvulus majalis* have no honey, but are used as a substitute for *Digitalis*. The *Corydalis*, because of self-pollination taken place); *Folium* multiflorum has honey secreted by septal glands and protected by the base of the tubular perianth; it is pollinated by humming-birds; the *Corydalis* is a S. American plant; the honey-bearing flowers; the *Corydalis* almost twice as large as the g.; both have rudiments of the opposite sex. + +About 100 genera are found in N. America, Europe, and Central Asia. + +**OFFICIAL:** "Dracena" blosom," a red resinous juice from the stem of *Dracaena*, and the roots of some Central American species of *Smilax*. The tubercles of *Smilax* contain a resinous juice which is used as a substitute for *Digitalis*. Fungaria, *Fungaria*, is a S. American plant; its leaves are used as food, except the young annual shoots of *Asparagus officinalis*, a shrew plant which is used as a vegetable. + +**Order 4. Amaryllidaceae (Narcissi).** The flower is epigynous, with an anther, while or white, petaloid perianth which forms a tube at its base. The stamens are inserted at different heights in the perianth-tube, and are directed to one side or another; they are usually united with one ovule (Eichhornia), in others reduced to one brachys with one ovule (Furcula). Fruit: a capsule or nut. Embryo as long as the abaxial, nearly oblong or ovoid; endosperm abundant; cotyledons two or three, according to nearly the same as in Zosteria. Spikes without floral-leaves. Many interstitial parts in the stem and leaf—in Greenhouse: Eichhornia canadensis, E.- canariensis, E.- nana; Furocula aquatica; Furocula aquatica var. subspicata; Furocula aquatica var. subspicata subspicata; Furocula aquatica var. subspicata subspicata var. subspicata; Furocula aquatica var. subspicata subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. subspicata var. +6/22 + +**LELIOLORE.** + +The majority, like these, are also perennial herbs with bulbs and scapes. The fruit and the other characters as in the Liliaceae. The external appearance is, however, very different. + +A. **AMARYLLIS** has bulbs and the leaves generally arranged in two rows ; the flowers are borne singly or in umbel-like im- +mersions, but the number of the flowers on the scape of the bulb is unlimited. Beneath the inflorescence is an *endocarpe* (Fig. 300).— +**Galanthus,** Snowdrop, has a polyphyllous perianth without corona; the three inner perianth-leaves are emarginate and shorter than + +Fig. 300.—Panacium cartham. + +the outer; the anthocarpe dehiscs apically. *Leucocis* differs in having the perianth-leaves equal to each other, and in having a cup-shaped perianth, +mainly or nearly polyphyllous, but somewhat zygomorphic. *Ornitho* ; +*Hemasthus* ; *Clicia.* —*Narcissus* has a tubular corona, a ligular structure arising from the perianth-tube exterior to the outer stamens. +In *Hyacinthus* the corona is tubular, and arises from the base of the inner +in spring from its edge. *Eucharis amonitans.* + +B. The perianth is usually polyphyllous, dry, folded, and in some +hairy, springing from a rhizome, generally with a divergence of 1/5. Flowers small, +perianth polyphyllous, persistent, on which account perhaps the Hypoxides may + +318 + +MONOCOTYLEDONES. + +be considered as the least altered type. The chief characteristic is that the embryo is separated from the hilum. Hypoxis, Cucurbita, (C. recurvata), a favourite ornamental plant, (S. E. Asia). + +C. Astarte (Astarte, Astartea, Astartea); stem long, leafy, often climbing. + +D. Trachelanthus (Trachelanthus); stem woody, usually rhizoidomously branched, with terminal, single flower; it bears numerous aerial roots which pierce the leaves and surround the stem. Stamens often (by splitting 6-18). High tailed stamens. + +E. Astarte. Very similar to the Bromeliaceae both in their distribution (nearly all American) and in external appearance. They appear as gigantic leaf- plants, with large leaves, which are either pinnate, palmate, or compound, inequilateral or linear, stiff, thick, and often thorny leaves, which form a large rosette; after the course of several (30-60) years the terminal inflorescence is developed, and then the plant dies away. In the Bromeliaceae also the inflorescence expands, a large quantity of sugar-containing sap is collected from a succulent by removing the terminal bud; this on distending yields a syrup (the sugar-sap). The leaves are often thorny. After the death of the plant the subtending lateral shoots survive and reproduce the plant—Agave americana, etc. + +F. Bromeliaceae. The 650 species are chiefly natives of S. America and S. America. Chilea, Hemionitis, *Eremilla* are from the Cape; *Nerium* from S. Europe; *Eremurus* from S. Europe; *Bromelia* from S. America; and *Lemna* and *Lemnophila* are especially from S. and Central Europe, and from the Canaries. + +Usoa, Laxiflora are ornamental plants: *Gambelia* silvestris; *Lemnophila*: *Nar- +cissus*: *Juncus*: *Lemna*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Lemnocharis*: *Alstroemeria*, Eremurus, Ortegas, Violette, etc. The vascular bundles of the various species of Agave (Agave rigidifolia; var. sieboldii; sand plant) are used for orchage, etc. + +Order 6. Bromeliaceae. The flowers are hypogynous, epigynous or perigynous; they are usually sessile into a short stalk and contain a staminate or staminode. The fruit is a capsule or berry with many seeds. Endosperm mainly, embryo small, at the edge of the endocarpus, but not excluded by it. + +Perennial bulbous plants with characteristic appearance (Fig. 310): - the stem is most often short, thick, and crowded by a rosette of many leaves, which are long, often very narrow, leathery, stiff, and with a glossy edge; they are usually channelled, completely closing round the base of the flower-stalks; they form a tightly closed hollow in which generally water is collected (the water collects things insulates the inflorescence and thus prevents the access of creeping insects, such as ants). The presence of numerous stellate water-conducting hairs on the leaves and on the surface of the stem and the layers of cells beneath the upper epidermis of the lamina form an "aquous tissue," which serves as a protection against the rays of sun and regulates the evaporation. The + +LILIIFLORE. +319 + +Fig. 311.—*Dactylos missione.* + +Stomata are often situated in furrows on the under-side of the leaf, and hence cause a striped appearance. They are mostly found in the tropics, especially from S. America, where they live partly as epiphytes on trees, partly in the clefts of rocks, often on the lower slopes, to which they firmly attach them selves by aerial roots; some are terrestrial. The stem is seldom tree-like (Papa, in Chili Hocita, in Mexico). The inflorescence is a terminal spike, raceme, or panicle, often with large and bright scrophularia-flower-bears. The flowers are without scent. + +W. B. + +Fig. 311.—Multiple-fruit of *Dactylos missione*. + +Y + +320 + +MONOCOTYLEDONES. + +The seeds, in the species whose fruit is a capsule, are often pro- +vided with wings (airsa, expansions, etc.)—Amanus autumn, Pino- +apple (W. Indies, Central America) is cultivated for the sake of its juicy, aromatic fruits, which conalese with their feathly bracts and form a large spike-like fruit-cluster (multiple-fruits; Fig. 311) +bearing many seeds. The seeds vary greatly developed.—Tulipanusa (T. amandae is a fila- +mentous, richly branched, rootless epiphyte hanging in masses from trees; Troop. Am.), Aechmea, Bolleraea, Pitcairnia, etc. + +Urea, the seed-capsule of the Pine-apple, in its native country, are used for the manufacture of cloth. + +Order 7. Hemerodromaceae. 120 species in all: part of the world except Europe; Asia Minor; India; China; Japan; the Borneoas; Indonesia; +and Amyrrhidaeum. Hemerodromus (Australia).—This order being Ophio- +pogon, Polypodiums, Saururias, and others. + +Order 8. The Iridaceae have epigynous, hermaphrodite flowers with petaloid perianth as in the Amyrrhidaeum, but the interior whorl of albumae is entire (Fig. 279); there is 1 style with 3 large, gene- +rally more or less leaf-like branches bearing the stigma. Ovary and capsule as in the Amyrrhidaeum and Lilaceae.—Perennial herbs; bulbs are rarely known; the leaves are usually basal only; they take their place in the style leaves are absent (except Crocus) as in the Iris, two- +rowed, quillant and sword-like. Flowers or inflorescences terminal. +The Iris (Fagia) has a rhizomatic rhizome. The flowers are borne +in the leaf-axils by fan-shaped leaves and petaloid perianth (hippodium). The +umbrella-like flower-heads are large and petaloid perianth may be seen a small projecting shelf (Fig. 312 a) having on its upper surface the stigmatic hairs. Beneath the branches of the style are 3 well protected stalked glands, and immediately outside these the exterior perianth is expanded into a cup-like sheath which shelters, +and the insects, endeavouring to obtain it through the narrow passages at +the base of the stamens, settle upon the outer perianth-hairs, which are bent-back +and thus protect them from injury. When they have obtained +their place on the anthers just above them, beneath the branches of the style; +they readily disperse over the whole flower-head where they unite, +not causing any hindrance in withdrawing since they unite with self- +fertilisation is thus avoided. The stylos hinderers lie close to the outer perianth-hairs and are very long—up to 6 cm., or even 15 cm.; the first form of flower is adapted for Eriophyllum strictum, the latter for bean—Cucius has vertical, tuberosus, underground stems + +1 The aggregation of the fruits of several distinct flowers into one mass. + +LILIIFLORE. +321 + +surrounded by the basal-lobules (corona), and terminal flowers; the limina-leaves are not opposite, but have two longitudinal furrows on the under side. The perianth is gamophyllous and funnel-shaped. The stylar branches (stigmas) are fleshy, rolled together in the shape of a horn, and split along the edge.—Gladiolus has compound leaves, with 3 to 5 leaflets, and produces almost bilabiate flowers, most frequently turning to one side. Position of the leaves as in the Iris—Dipterocereus has 2 fertile and 1 barren stamen; *Hemodoradion* has a unilocular ovary with 3 partial placentae. Cyptoe and Tigrida have bulbs. + +**Fig. 311.—Fole pseudodiscus.** One external and two internal perianth-leaves, and one of the stamens, which is sterile. The corona is composed of 3 basal-lobules ; 2 stylar-lobules ; a stigma ; a stamen. The corolla is seen in longitudinal section. + +710 species; chiefly in the countries round the Mediterranean, and in Africa, especially the Cape (Gladiolus, Ferraria, Moena, Galicia, Sporadis, Antholopis, Tristium, Leia, etc.), America (Iris), Asia (Iris, *Gymnadenia*, *Tigrida*, *Gymnadenia*). A great number are ornamental plants: the cultivated *Oxeye*-species are from the South of Europe and Asia; *Gladiolus communis* from France; *G. italicus* from Italy; *G. luteus* from Spain; *G. bulbosus* from Germany. The native species of Iris are L. pseudodiscus (yellow) and L. festifilium. + +**ORIENTAL :** the stigma of *Crocus sativus* (Ortental, cultivated in France, Spain, Italy, and Austria), used as a coloring matter; **saffron**; the rhizomes of the th European *Iris germanica*, paludosa, and germanica (*Ornithogalum*). + +A diagram showing the structure of a flower with parts labeled. + +322 +MONOCOTYLEDONES. +Order 9. *Dioscoreaceae.* Perennial herbs with fleshy, often very large tuberous rhizomes (or roots); twining stems; leaves stalked, often arrow- or heart-shaped, lobed, palmered and finely reticulate as in the Diosciyledons (Fig. 315). The flower is *dictyate* (most frequently dictyose), regular, epigynous, embot, and + + +A: A tuberous rhizome. +B: A flower bud. +C: A flower. +D: A fruit. +E: A seed. +F: A leaf. +G: A leaf base. +H: A leaf petiole. +I: A leaf blade. +J: A leaf margin. +K: A leaf venation. +L: A leaf stipule. +M: A leaf axil. +N: A leaf sheath. +O: A leaf trace. +P: A leaf trace node. +Q: A leaf trace internode. +R: A leaf trace bundle. +S: A leaf trace bundle node. +T: A leaf trace bundle internode. +U: A leaf trace bundle sheath. +V: A leaf trace bundle sheath node. +W: A leaf trace bundle sheath internode. +X: A leaf trace bundle sheath sheath. +Y: A leaf trace bundle sheath sheath node. +Z: A leaf trace bundle sheath sheath internode. +AA: A leaf trace bundle sheath sheath sheath. +BB: A leaf trace bundle sheath sheath sheath node. +CC: A leaf trace bundle sheath sheath sheath internode. +DD: A leaf trace bundle sheath sheath sheath sheath. +EE: A leaf trace bundle sheath sheath sheath sheath node. +FF: A leaf trace bundle sheath sheath sheath sheath internode. +GG: A leaf trace bundle sheath sheath sheath sheath sheath. +HH: A leaf trace bundle sheath sheath sheath sheath node. +II: A leaf trace bundle sheath sheath sheath sheath internode. +JJ: A leaf trace bundle sheath sheath sheath sheath sheath. +KK: A leaf trace bundle sheath sheath sheath sheath node. +LL: A leaf trace bundle sheath sheath sheath sheath internode. +MM: A leaf trace bundle sheath sheath sheath sheath node. +NN: A leaf trace bundle sheath sheath sheath internode. +OO: A leaf trace bundle sheath sheath node internode. +PP: A leaf trace bundle node internode. +QQ: A leaf trace bundle internode node. +RR: A leaf trace bundle internode internode. +SS: A leaf trace bundle internode internode internode. +TT: A leaf trace bundle internode internode internode internode. +UU: A leaf trace bundle internode internode internode node. +VV: A leaf trace bundle internode internode internode internode node. +WW: A leaf trace bundle internode internode internode internode internode node. +XX: A leaf trace bundle internode internode internode node internode. +YY: A leaf trace bundle internode internode node internode internode node. +ZZ: A leaf trace bundle internode node internode internode node internode node. +AAAAA: A leaf trace bundle node internode internode internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode node internode + + +of a greenish colour, but otherwise typical (*Pell*+3, and *A3*+3, or *G3*); in most instances 2 ovules are placed one above the other in each loculus. The inflorescence is a spike or raceme, sometimes richly branched and paniculate.—The order approaches most nearly to the Amaryllidaceae. + +**SITAMINSE.** + +323 + +*Yam* (Bryony) has a berry, *Dioscorea* (Yam) a thin-walled, bunched or twined upper (Fig. 315). Both have subterranean or aerial tubers; the yams often also develop lateral tubers in the axis of the foliage-leaves; tuberous roots are said to occur in *D. batatas*. The tubers of many species of Yams (*D. batatas* from China and Japan, *D. alata*, from India, *D. bulbifera* from Africa), are very important sources of food in the tropics, especially the first important - *Tutunadura*; *Rajania*; The tuberos stem of *Zuma commans* and *Tutunadura elephantus*, and some species of *Streptocarpus*. The tubers of *D. batatas* are usually white. Shoots are developed from adventitious buds; in *D. elephantus* the stem is aerial, and covered with thick scales of cork, regularly arranged, and separated by grooves. + +Tropical order (107 species) 5 genera (*Zuma commans* and *Bourneolae* provided in Europe). + +Family *Scitaminee.* + +The flowers belong to the ordinary monocotyledonous type. They are hermaphrodite, epigynous, and have either a petaloid perianth, or calyx and corolla; they are, however, zygomorphic or symmetrical, and of the families most frequently only one or other of these organs being more or less modified by petaloid stamens. The ovary has 3 loculi, more rarely it is unilocular with the suppression of 2 loculi. Endosperm is absent (except *Ziphorensis*); but, on the other hand, there is a large embryo-sac which is not placentally situated *pericarpial* kerma with rhizomes; leaves large, distinctly divided into sheath, stalk, and blade, the latter being more or less stipulate or lanceolate, entire, with pinnate venation, and always having a nectary at the base of each leaf-stalk; the sepals are erect towards the apex, and giving off numerous branches which run outwards towards the margin, at a larger or smaller angle; these lateral axes are closely packed, and parallel, but with only weak connexion between them; the petals are free; therefore, are easily torn pinnately (Figs. 314, 317). The leaf-buds close tightly round each other and form a false stem. + +This very natural family comprises orders closely connected with one another, but not itself nearly allied to any other family. +First in the series stage. + +Order 1. *Musacee.* The petaloid perianth is strongly zygomorphic, the anterior leaf being very large (a kind of "lakelism"), the posterior one small; only the posterior stamen is wanting, or is rudimentary, the other five are developed, and + +324 +MONOCOTYLEDONES. +have quadrilocular anthers; ovary, 3-locular. Seed with straight embryo in nearly peripyle. + +The best-known genus is Musa, the Banana (Fig. 314). From the short rhizome arise enormously large, spirally-placed leaves, whose sheaths envelope one another, and form an apparently aerial + +A banana plant with large, spirally-placed leaves. +**Fig. 314.—Two Banae-palms.** + +stem, several metres in height. The inflorescence is a terminal spike, which is placed spirally, and sometimes slightly conoidly coloured; in the axils of some of the lowest flowers are situated in two transverse rows (accessory buds); the lowest flowers in the inflorescence are $V$, the central ones $V$, the upper + +SCITAMINEE. +325 + +ones, so that fruits are only found in the lower region of the inflorescence, the remaining portion persisting as a naked axis after the floral-leaves and flowers have fallen off; the inflorescence terminates in an ovoid bud formed by the flowers which have not yet opened (known as the "posterior one"). The two leaves are united (except the posterior one). The fruit (known as a "Banana") is a berry, having the form of a smooth, short, three-angled cucumber (as much as 30 cm. in length) inside the tube of the flower-bud. The fruit is very sweet and is developed in the cultivated species. Several species are culti- +vated in the Tropics for the sake of the fruit (M. paradisicae, M. sapientum, M. cerasifera, M. cerasifera var. alba), but their home is, no doubt, the Tropics of the Old World; they were introduced into America before the arrival of Europeans. These fruits are hardy, leathery fruits. + +In Musa, the barren, posterior stamens belongs to the inner whorl; and also in Streitzia and Ruscaceae; the latter may have all 6 stamens developed. In Heliconia and Costus, the outer whorl consists of 6 stamens; the perianth-leaves are differently arranged, and there is only one ovule in each loculus. The three latter genera have dry fruits and leaves arranged in two rows on opposite sides of a central axis; consequently, the foliage-leaves form an enormous fan--Tropical--about 50 species. + +The order may be divided as follows:—1. Musaceae: Musa, +Heliconia, Costus; 2. Heliconieae: Heliconia in the New World. + +Order 2. Zingiberaceae. Perennial most frequently divided into calyx and corolla. Calyx generally 3-lobed or 3-parted; stamens (the posterior, Fig. 315, belonging to the inner whorl) with quadrilateral anther, with a long narrow furrow; the 2 stamens in the outer whorl are staminodes, the median one (the anterior) is sterile; in some species of Costus, there are staminodes of the inner whorl which form the "labelum" (Fig. 315 lab.), which usually is the same as the corolla; this labelum is often lobed and is often bilobed. Ovules many. The fruit in some is leathery, 3-valved capsule, + +Fig. 315.--Diagram of a Zingiberaceous flower (Heliconia). A, bract; B, bract; C, tubular calyx; D, corolla; E, stamens: $p_1$, $p_2$, $p_3$ the petals; $a_1$, $a_2$, $a_3$ anthers; $b_1$, $b_2$, $b_3$ filaments; $c_1$, $c_2$, $c_3$ staminodes (formed by two staminodes); d, fertile ovary; e, style; f, stigma. The corolla is in the centre of the diagram. + +326 +MONOCOTYLEDONES. + +with localicial dehisence; in others it is more or less berry-like and indolent, or irregularly dehiscent. Straight embryo.--The aerial stem is seldom developed to any extent, and the inflorescence, which are (compound) spikes or racemes, often with clustered flowers, is usually produced from the rhizome. The leaves are arranged in two rows.--The ovary in a few instances (Globos and others) is unilocular, with 3 parietal placentae. + +They are perennial plants with bushy and tuberous rhizomes, which are used as condiments and in medicine as sources of their pungent and aromatic properties and also for starch, dye, etc. Ornamental: *Rhizoma* of Zingiber officinale (ginger), *Cymbopogon* citratus (clove), *Cymbopogon* citratus (clove), *Curcuma longa* (Turmeric, a spice), and *C. zedoaria* C. zedoaria (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric), *C. zedoaria* (turmeric). The leaves are arranged in two rows.--The ovary in a few instances is unilocular, with 3 parietal placentae. + +Order 3. +**Cannae**. +American herbs without aromatic properties. +Flowers asymmetrically symmetrical. +Stamens numerous. +Stigma terminal. +Capsule straight. +Ornamental plants: Canna indica, etc. + +Fl. +326 +Fam. +306. +Flower of Canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; / canna; +327 +Fam. +306. +Flower of Cana; +328 +Fam. +306. +Flower of Cana; +329 +Fam. +306. +Flower of Cana; +330 +Fam. +306. +Flower of Cana; +331 +Fam. +306. +Flower of Cana; +332 +Fam. +306. +Flower of Cana; +333 +Fam. +306. +Flower of Cana; +334 +Fam. +306. +Flower of Cana; +335 +Fam. +306. +Flower of Cana; +336 +Fam. +306. +Flower of Cana; +337 +Fam. +306. +Flower of Cana; +338 +Fam. +306. +Flower of Cana; +339 +Fam. +306. +Flower of Cana; +340 +Fam. +306. +Flower of Cana; +341 +Fam. +306. +Flower of Cana; +342 +Fam. +306. +Flower of Cana; +343 +Fam. +306. +Flower of Cana; +344 +Fam. +306. +Flower of Cana; +345 +Fam. +306. +Flower of Cana; +346 +Fam. +306. +Flower of Cana; +347 +Fam. +306. +Flower of Cana; +348 +Fam. +306. +Flower of Cana; +349 +Fam. +306. +Flower of Cana; +350 +Fam. +306. +Flower of Cana; +351 +Fam. +306. +Flower of Cana; +352 +Fam. +306. +Flower of Cana; +353 +Fam. +306. +Flower of Cana; +354 +Fam. +306. +Flower of Cana; +355 +Fam. +306. +Flower of Cana; +356 +Fam. +306. +Flower of Cana; +357 +Fam. +306. +Flower of Cana; +358 +Fam. +306. +Flower of Cana; +359 +Fam. +306. + +The diagram of the androecium of + +SCILIMINEE. +327 + +the Cannaceae and Marantaceae may be represented in the follow- +ing manner (calyx, corolla and gynoeceum being omitted)— + +CANNACEAE. + +Marantaceae. + +37 +at +w +at +w + +at +w +at +w + +at +w +at +w + +The labellum of the Cannaceae corresponds with the hood of the Marantaceae and not with the lobes of the Maranta. + +Order 4. *Marantaceae.* The flower is symmetrical. Only 1 or 2 of the 3 stamens in the outer whorl are present as stami- +nodes ; in the inner whorl 2 are petaloid and of the sixth stamen + +Fig. 317.—Coffea arabica. + +one-half is developed as a staminee and the other half bears a bilobular anther. One ovule only in each loculus. The style is a strong stalk and at its base is a large, cup-like lamina (hood) of the inner whorl; later on it springs elastically forward towards the other staminee (inner-wing) of the same whorl. The stigma is very oblique or 2-lipped. Two of the three loculi of the ovary, in some species, are empty; in others they are filled with seeds in two rows, with sheath, stalk, and blade (Fig. 317); at the base of the last is a characteristic swelling (articulus).—*Phragmium, Calathea, Stremonia, Caranta, Sarracenia, etc.* +about 139 species; tropical, especially America. The stalk of the rhizome of *Monstera arenariae* is verrucous, "West Indian Arrowroot." + +A diagram showing the structure of a Cannaceae flower. + +325 + +**EUCOCOTYLEDONES.** + +**Family 7. Gynandrace.** + +The flowers are hermaphrodite and constituted on the ordinary 8-merous, pentacyclic type with petaloid, epigynous, strongly epymorphic perianth, and generally one-stamened by the suppression of the stamens of the corolla. The genus is derived its name from the fact that the stamens are united with the petals in a "straight column" (except *Trunmanna* uniflora). All are herbs ; many grow as epiphytes on other plants. + +This family and the Betulaceae occupy correspondingly high positions among the flowering plants. Of these two families, only may be placed close together, although one cannot be derived from the other. The first of the two orders is very small, but the second is very rich in species. The Agastachis can be best compared to the *Lilium* of the first order. + +Order 1. *Bettulaceae*. This order forms a transitional link between the Gynandrae and the epigynous Liliiflorae (*Anasylilaceae*), having in a closed perianth, and 6–3 stamens; but some have a single stamen, and others have no stamens at all (the whole being very large). The ovary is most frequently unilocular with three parietal placentae; but in some it is 3-locular with axile placentation. Capsule. Seeds oval, small, with endosperm. The relationships of this order are uncertain, especially in the very imperfectly developed embryo and in the ovary. Small, tropical herbs (50 species); some are saprophytes. + +Order 2. *Orchidaceae*. The epigynous, petaloid perianth is strongly epymorphic in having a long tube-like foot of the interior whorl, the lip (labellum), differing from all the other leaves in being much larger than the others (except *Aporostre*); the position of the labellum is very frequently reversed, becoming more or less downwardly by the twisting of the ovary (Fig. 318 A). Only 1 of the stamens—-the median one—is developed and bears an anther (by the twisting of the ovary it is + +Fun. 315.—Diagram of an Orchid-flower. F, Gynandraeae. Bijugum-ovatum : anther ; stigma ; anther at the base of which is shown the position of the parts which have been removed. +A +B + +GIRANDELLE. + +329 + +turned posteriorly and upwards); the others are entirely wanting (indicated by * in Fig. 318 A) or present as staminodes (Fig. +318 A, over) (except Apotestus, Cyprigynales); the filaments are united with the style to form a column (Fig. 318 B), the stylar-columna¹ (gynostemium), and the anther (Q) is then placed on its apex and slightly below the stigma (R). The pollen-grains are monads; the pollen-grains do not separate (except Apotestus, Cyprigynales) but remain united either in tetrams or in masses, which correspond to a pollen-structure (C, D, B), or to the pollen-grains, or both, each of the two anthers being thus formed to form one or a few wax-like masses (pollen-masses, pollinia). The 3 carpels form a unilocular ovary with parietal, deeply fissled placenta (except Apotestus, Sideritis, etc.). Only the two lateral carpels are provided with a median line (Fig. 318 A, R), while the one lying in the median line, which is situated just within the anther (Fig. 318 A), becomes either rudimentary or degenerate into a small nectary gland (Fig. 318 C), on which the sticky bodies (glándulae) arise; by aid of these the concentrated pollen-masses may be glued to the insects which visit the flower, and pollination is thus secured (in Apotestus and Cyprigynales the carpels each contribute to the formation of the stigma). The fruit is a capsule, which is usually bivalved, of which 2 valves are broader and baren the placenta, and 3 alternating with them are narrower and barren (except Familia). The very numerous and exceedingly small seeds have no endosperm, and have a some- +what thickened testa, which may be free or covered by transverse organs. The tests are membranous and loose. + +The Orchids are all perennial herbs with diverse habits and varying morphological structure (see the genera); the leaves are either entire or pinnate, simple or compound, and the flowers are numerous in all cases racemes or spathes (sometimes sheathed), or solitary, extending +bracts, but without bracteoles. + +The forms which are the least described are detailed first. +1. Anther (Q) and stigma (R)—the leaves are almost alike and free. +The column is straight, with 3 equally-developed stigmas. **Neu- +cielia** has 3 perfect stamens (1 median of the outer whorl, and +2 lateral of the inner whorl); **Apotestus** has only 2 perfect (inner +whorl) and one imperfect (median of the outer whorl), which how- +ever according to Pîssier, the column is the prolongation of the floral-axis +behind the anther. The anther is smooth, and is not formed by the coalescence of +sperophytes (filament and style). + +1 + +330 +MONOCOTYLEDONAE. + +ever may be entirely wanting. The 5 posterior stamens are entirely suppressed. The pollen is powdery. The ovary is 3-locular with axile placentae. 7 species (Tropical East India, Australia). + +2. *Cyprideileum.* The flower is strongly zygomorphic with a large boat-shaped labellum. There are two perfect stamens being longer than the ovary, and the three staminodes on the posterior stamen of the outer whorl is transformed into a large, barren, shield-shaped body (Fig. 319). *Solenodendrum* has a 3-locular ovary, but *Cyprideileum* (Ludisia-stippe) has a unilateral ovary with 3 partial placentae—the typical structure for the Orchids. + +A diagram showing the structure of a flower, likely representing Cyprideileum or a similar orchid species. + +Fig. 319. *Cyprideileum* stippe. A front view of the flower. A lateral view after the removal of all the perianth-leaves with the exception of the labellum, which has been detached in order to show the stamens and pistil. $a$ = anther; $b$ = ovary; $c$ = style; $d$ = pistil; $e$ = petal; $f$ = lip; $g$ = lobes of the labellum; $h$ = staminode; $i$ = staminode; $j$ = staminode; $k$ = staminode; $l$ = staminode; $m$ = staminode; $n$ = staminode; $o$ = staminode; $p$ = staminode; $q$ = staminode; $r$ = staminode; $s$ = staminode; $t$ = staminode; $u$ = staminode; $v$ = staminode; $w$ = staminode; $x$ = staminode; $y$ = staminode; $z$ = staminode. + +The pollen-granules are aggregate (not in tetrad) and all the 3 lobes of the atrorubrum are constructed to receive them. This group is therefore, next to the Apostasoidae, the least modified among the Orchids ; in all the following groups, one of the lobes of the stigma is differently developed from the others, and there is only one stamen.—Terrestrial orchids have a single stigma, and this is often so long that its forcible entrance to insects into the boat-shaped labellum (Fig. 319)’s at 1, and their escape at 26 (at 27) where the anthers are situated ; in this way the stigma will be protected from rain-water, and its pollen-granules are surrounded by a sticky mass in order that they may adhere to the insects. +1 + +GYNANDROE. + +3. +**NEOTECTI.** The majority are terrestrial Orchids with creeping, sympodial rhizomes; the blades of the leaves are not de- +tached from the stem at joints, and have convolute vernation. +The anthers do not drop off, but persist in the withered con- +dition; their apex is brought in contact with the costellum (acro- +tonous Orchid); or they are attached to the leaf-blade, which, +however, often hang loosely together in pollen, attached to a +sticky part of the rostellum ("adhesive disc"), so that they adhere to the insects, and are by them transferred to the stigmas. +Sporogonium (Fig. 300 A, B) is a terrestrial orchid, with a +little chlorophyll in colour, has no foliage-leaves, and lives mainly as a sapro- +phyte; the rhizome is studded with unbranched, fleshy roots which may form bulbs at their extremities. --Famula ciliosa by aerial roots. The fruti + +A diagram showing the structure of a flower of Orchis mascula. +Fig. 300.--A Flower of Orchis mascula (front view). a, a short cup; b, the cup; c, n the stigma; d, the anther; e, the pollen-grain. B. A flower of Sporogonium (front view). a, a short cup; b, the cup; c, n the stigma; d, the anther; e, the pollen-grain. F. A flower of Euphrosyne (front view). a, a short cup; b, the cup; c, n the stigma; d, the anther; e, the pollen-grain. + +is flaky and hardly open, or does not irregularly.--Euphrosyne, +Cephalotricha.--Epipogon and Linodorum are saprophytes without chlorophyll. + +4. +**OPHREDEI.** Anthers 2-locular, not falling off, on a very short stem connected at the apex (acrotomous Orchid), while in all other Orchids it is connected at the apex (acrotonous Orchids). The pollen-grains in each loculus are united into small "masses" (massae), each of + +332 + +MONOCOTYLEDONES. + +which corresponds to a pollen-mother-cell in the anther, and which hang together by elastic threads (Fig. 320 C, E). Each pollinium is attached at the base by a stalk (caudicle) to an adhesive disc, formed by the same stigma (cauligma), and is easily liberated by the pressure of the anther. The caudicle, which is formed in an anther-lobe, together with its caudicle and adhesive disc, is termed "pollinarium" (Fig. 320 C, D). ---All Ophioglossa are terrestrial with fibrous roots, two of which are present in the first year, and one in the second (and possibly the third year) containing the nourishment for the flowering-shoot of the year, and a young one which is intended to contain the reserve material for the following year. Inflorescence terminal. + +Orchis, *Orchis* × *Habenaria*, *Habenaria*, *Habenaria*, *Pipilia* is attached to its own adhesive disc, the disc being enclosed in a common pouch formed by the rostellum (Fig. 320 C, D). Tubers ovate, umbellate; 5-8-10-15-20-25-30-40-50-60-70-80-90-100-110-120-130-140-150-160-170-180-190-200-210-220-230-240-250-260-270-280-290-300-310-320-330-340-350-360-370-380-390-400-410-420-430-440-450-460-470-480-490-500-510-520-530-540-550-560-570-580-590-600-610-620-630-640-650-660-670-680-690-700-710- +72 +73 +74 +75 +76 +77 +78 +79 +8 +81 +82 +83 +84 +85 +86 +87 +88 +89 +9 +91 +92 +93 +94 +95 +96 +97 +98 +99 +1 +11 +12 +13 +14 +15 +16 +17 +18 +19 +2 +21 +22 +23 +24 +25 +26 +27 +28 +29 +3 +31 +32 +33 +34 +35 +36 +37 +38 +39 +4, +41, +42, +43, +44, +45, +46, +47, +48, +49, +5, +51, +52, +53, +54, +55, +56, +57, +58, +59, +6, +61, +62, +63, +64, +65, +66, +67, +68, +69, +7, +71, +72, +73, +74, +75, +76, +77, +78, +79, +8, + +E. 8. +E. 9. +E. 1. +E. 2. +E. 3. +E. 4. +E. 5. +E. 6. +E. 7. +E. 8. +E. 9. +E. 1. +E. 2. +E. 3. +E. 4. +E. 5. +E. 6. +E. 7. +E. 8. +E. 9. +E. 1. + +F. 8. +F. 9. +F. 1. +F. 2. +F. 3. +F. 4. +F. 5. +F. 6. +F. 7. +F. 8. +F. 9. +F. 1. +F. 2. +F. 3. +F. 4. +F. 5. +F. 6. +F. 7. +F. 8. +F. 9. + +G. G. + +H. + +I. + +J. + +K. + +L. + +M. + +N. + +O. + +P. + +Q. + +R. + +S. + +T. + +U. + +V. + +W. + +X. + +Y. + +Z. + +A. + +B. + +C. + +D. + +E. + +F. + +G. + +H. + +I. + +J. + +K. + +L. + +M. + +N. + +O. + +P. + +Q. + +R. + +S. + +T. + +U. + +V. + +W. + +X. + +Y. + +Z. + +A. + +B. + +C. + +D. + +E. + +F. + +G. + +H. + +I. + +J. + +K. + +L. + +M. + +N. + +O. + +P. + +Q. + +R. + +S. + +T. + +U. + +V. + +W. + +X. + +Y. + +Z. + + +Coralarihize = Coralarihizus + +GYNANDRE. 333 + +ascending shoots, which bear the foliage-leaves, may vary, but they very often swell and assume the form of a tuber, which persists for several years fresh and green after the leaves have fallen off (Fig. 82). *Vanilla* is an exception (fig. 83), for its tubers are very small and of a short duration. A large number of species is found in calyptero-silva. + +Pollination takes place principally by the insects, but self-pollination occurs occasionally. The flowers are visited by a long-hanging stage for the insect visitors, which, on sucking the honey, cause the adhesive discs, with the pollinia adhering to them, to adhere to the surface of the flower, and so carried to other flowers. In some species parts of the flower are sensitive or irritable, which has some connection with the pollination. Without doubt there is a great variety of forms among these plants which are closely connected with the infinite multiplicity of forms; Darwin (1862) has already shown an enormous variety, never seen even of before, in the European species. The genus *Cattleya* has $f$, $q$, and $z$-plants with flowers of such different characters that they cannot be considered as varieties (figs. 84, 85). *Cattleya* (Monanthos), *Platanthera* is pollinated by hawk-moths; *Ophrys*, by flies; *Epipactis luteola*, by wasps; *Orchis*, by bees, especially humble-bees, etc. + +The flowers are usually small and fragrant, and their petals are exceedingly small and light. Many species moreover have peculiar, cluster-like, or cup-like flowers. The orchid-fruit is ovary, which ejects the seeds in a manner similar to the clappers of the Leveret. + +The cattas are few, mostly as ornamental plants in conservatories. The tubers are used as food by the natives of Brazil, who call them "sacres" or "sacres" and use them as "sages." The fruits of *Vanilla planifolia* are used as condiments and differ from other Orchid-fruits in being rather flimsy and dehiscing irregularly; the seeds are very small, shining and black. + +![Image](image) + +Fig. 82.—Chilea bracteosa. + +334 + +**DICOTYLEDONES.** + +**Class II. Dicotyledones.** + +In this class the **embryo** has 2 seed-leaves, a rule with which there are few exceptions (e.g. *Feverfew*, *Cytisus*, *Flueggea*), certain species of *Euphorbia* (which have 3 leaves); and a few mostly parasitic forms, e.g. *Monotropa*, *Orchisba*, *Pyrola*, entirely without cotyledons. + +On germination the cotyledons nearly always raise themselves above the ground as green, assimilating leaves and are then termed "true leaves" (or "true cotyledons"); but in the subterranean ground or hypogean which are always buried. The structure of the seed varies (endospermous or exospermous); the embryo may be straight or curved. In many instances the primary root grows upwards, and the secondary roots grow downwards, or vice versa; internally (in annuats, bionials, many perennials, especially woody plants) but in a large number of herbaceous perennials, which have rhizomes, the root behaves very much as in the Monocotyledons. This mode generally increases in difficulty by means of a cambium. + +The stem, when seen in transverse section, has its vascular bundles arranged in a ring; in reality, however, they form a kind of cylinder, which is divided into several layers or zones, and thickening takes place by means of a cambium; annual rings are formed in the perennial stems. There is a rich and very varied form of branching. The two first leaves of a shoot (fore-leaves) are placed at right angles to each other; left and right arrangement is found in the two first leaves developed on the flower-stalk; and these are, as a rule, only two; they are found below the enlyx and are usually termed the "bracteoles." It has become customary to represent this arrangement by the letters a and b, according to the sequence of growth, an arrangement that some these letters will be employed in the following diagrams. + +The arrangement of the leaves varies very much; there is also a great variety in the number of leaves and their position, just like the limoniums, with parallel venation; but in the Monocotyledons, are seldom met with, as also the large sheaths (though the sheath is well developed in the Umbelliferous plants); stipules occur much more frequently. + +The type which is most common is monopetalic, but achyric or hemicyclic forms also occur. The type which may be taken as a basis consists in the majority of instances, as in the Monocotyledons, of 5 whorls, of which the 4 outer ones (enlyx, corolla, and the 2 + +**BUCYLLERIDACEAE.** + +335 + +*whorls of stamens)* are most frequently 4 or 5 in number and placed in regular alternation, whilst the innermost one (the *carpele*) has generally fewer members, probably on account of space (Figs. 360, 361, 421, 429, 487, etc.). Trimerous (Figs. 384, 387, etc.) flowers, or those in which the members of the flower are three in number, are very rare; tetramerous flowers are common flowers; other numbers are rare. +It is of the greatest importance in connection with the relative position of the members of the flower to the axis and bract (orientation), whether the bracteoles are present or not. When they are present, they are usually closely, or are typically absent. If there are 2 bracteoles present, then their position in a pentamerous flower is often as follows: the first sepal turns obliquely forward, the second is posterior and median, the third is anterior and median, the fourth is anterior and oblique (transverse); quincuncial estivation is often found in these buds (Figs. 360, 429, 471, 475, 584). The first and third leaves, in the following chapters, are most frequently alluded to as the *anterior*, the fourth and fifth as the *posterior*. The median leaf, which lies with its median sepal in the front, occurs for instance in *Papilionaceae* (Fig. 511), *Lobeliaceae* (Fig. 504), *Rubiaceae*. If any bracteoles are present below a tetramerous flower, the relation is generally that two next ones transversely (Fig. 393), and the corolla then adopts a diagonal position (Fig. 397); but a diagonal position of the calyx generally shows that the flower is not strictly speaking, tetramerous, as in *Primulaceae* (Fig. 360), *Verbenaceae* (Fig. 502) etc. + +If the calyx is not typically pentamous, then the position of the sepals is changed accordingly, and the two outer sepals endeavour to assume the position which the bracteoles would otherwise have occupied, e.g., in *Primula* (Fig. 547). Other possibilities are also found when the number of bracteoles is more or less than two. + +The leaves which follow the sepals occupy definite positions with regard to them, and this is always regular. In some arrangements of leaves may be mentioned here; where the flower is "diploclenous", that is, has two whorls of stamens (thus, Su., Pn., An.-n.), these may be arranged in two ways. Either the first-mentioned whorl stands directly behind the second (that is "epispermous"), and in the outermost whorl, and in this case a regular alternation takes place between sepals, petals and the two whorls of stamens, +w. n. + +335 + +**Dicotyledonous** + +which is also continued into the carpels if their number is the same as that of the other whorls; the carpels are then placed opposite the sepals (Fig. 278) and the flower is *isomerous* and *Gn* should be added to the formula above. Or, the calyx-stamens form the first whorl, and the stamens and carpels, which are sub-sequently formed (*epipetalous*) and *staminal*, stand outside those (Figs. 300, 429); if the number of carpels is the same as that of the preceding whorls, they are often placed *rigidly* at front of the petals and sepals (Fig. 301). The arrangement of this kind of arrangement is termed *Dicotyledonous*, and the second *Oblipetalous*. Both arrangements may be found in one and the same order, e.g. Carpinus bifolia. The sinu and reticulation of the leaves, nor also the contact with other members in the early stages of their development, play an important part in determining the arrangement. + +The great number of structural arrangements found in this enormously large class, may, as is the case in the Monocotyledons, be further varied by suppression and division of certain leaves (especially those of the perianth), and such variations will occur in the following (Figs. 500, 568—569, 426, 441, 445, etc.). + +The Dicotyledons were formerly divided into three sub-classes : Apatetale (those without corolla), Symptale or Gamopetalate (those with the perianth), and Choriptale (those with a perianth but without it). This division has now been abandoned because it has been proved that the Apatetale were merely reduced or incomplete forms of the Choriptale, and they have therefore been distributed among the latter. + +With regard to the Symptale (or Gamopetalate) it may be stated that they form to a very great extent a closely connected and natural group, having in common not only the character that the corolla is composed of two parts, but also a great many features; as persistent calyx, cyclic flowers with the formula Ss, Ps, As and as a rule G2, the two carpels being aimed to form the ovary ; scads with a third carpel being wanting; etc., etc. These characters must therefore be considered as an independent sub-class, and must be placed at the close of the system of classification as the forms which presumably have arisen the latest. In the future systems of classification it will probably be found that this group, and the first families of the Symptale, the Bicornus and others will for instance be to a certain extent united with the families or orders of the Choriptale. The Symptale may certainly be con- + +Salicifolium. 337 + +sidered as the youngest type, the strongly pronounced metanom- +phosis supporting this theory, as also the formation of the integu- +ment of the ovule, the one thick integument being undoubtedly +derived from the coalescence of two—a holochalazymous ovule, etc. +The Apatelae and Choripetales are united into one sub-class. The +two of these sub-classes differ from each other, the structure of the flowers presents many differences, and the ovules have a rule 2-integuments and a large mesocarp. Con- +siderable uncertainty still prevails regarding the arrangement and +the relationship of the individual families of the Choripetales, and +several authors (e.g., H. Münster, J. F. Schultze) have proposed +the best arrangement arrived at so far has been adopted here. + +At the beginning of the book a review of the orders of the +Dicotyledons will be found. + +Sub-Class I. Choripetalea. Petals free. + +Family I. Salicifolium. + +Trees and shrubs, which, in the structure of the vegetative shoot +and the catkin-like inflorescences, resemble the Quercifolium, but +the structure of the flower differs so much from them, that the + +A drawing of a plant with a long stem and leaves. +Fig. 32.—Male and female suckers of Salix argentea. + +only order brought under this heading—Salicaceae—well deserves to be separated and to form a family of its own, the sources +relating to this fact are numerous. In addition to this, Malpighiaceae +also deserve to be placed in a special family, the name *Juncaceae* (*Cattl- +leaverae*), hitherto applied to all of these plants, cannot be retained as the name +of a family. + +There is only one order. + +338 +SILICULULEONES. + +Order: *Salicaceae* (Willows). Trees with simple, scattered, stigmate leaves. Dioecious. The flowers are arranged in simple inflorescences (spikes or racemes) which are termed catkins, and which fall off as a whole after flowering (♂) or after the ripening of the fruit (♀) (Fig. 322). The perianth is very imperfect¹ or wanting, particulate, and consists of two series of stamens and one series of stigmas without any trace of a carpel (a, b, c); the ♀-flower has a free bicarpellate ovary, sessile, and formed from 2 lateral carpels with a persistent (*median*) placenta and generally ± ovulate; the style divides into two branches, each bearing a single stigmatic lobe; the capsule and the very small seed ball bear a tuft of hairs at the base. *Endogamum* absent.—The catkins are situated on dwarf-bushes, which in some species often develop before the leaves and bear at their base only scale-leaves; in others foliose-leaves are borne beneath the catkins. The rape-
+A diagram showing the structure of a willow flower.
+Fig. 323.—*Salix*: male flowers of *S. pentandra* (a), *S. erinacea* (b), *S. rubra* (c); female flowers of *S. erinacea* (d), *S. suprapina* (e), *S. mulleri* (f). + +tireful bud commences with 2 bud-scale which are united on the exterior side into a small cup-like operculum enclosing the bud proper. The seed-hairs spring from the funicle. + +*Sulia* (Willow) has short-stalked, most frequently lanceolate leaves and erect catkins with undivided bracts (Fig. 325). The flowers are naked; 1 (in a) or 2 yellowish glands situated in the middle of the bracts; the perianth is wanting; the stamens are inserted laterally like the carpels in the ♀-flower. Various forms are seen in Fig. 326.—The terminal bud of the branches often aborts regularly, the uppermost laterals being replaced by lateral buds. + +*Populus* (Aspen, Poplar) has long-stalked, more or less round or cordate leaves with drawn-out apex; catkin pendulous; lobed + +¹ This is Eichler's view.—According to Dendrology the perianth is absent; at the base of the branch, a nut-like or cup-like disc. Populus holds the same view. According to Eichler the perianth is absent, but there is a disc cap-like, or reduced to a single toothed scale. + +4 + +**CASCARINIFLORE.** 339 + +bracts: perianth cup-like with oblique edge: stamens usually numerous: stigmae often divided: $f$. -pseudore (Agena) has received its name from the theme of the heaven: $q$. -to take shape as an apex leaf. + +**FOLIATION.** The Foliage are white, yellow, or green. Willow have silky foliage and are usually deciduous. The stalks of the Willows, especially the $f$, are more conspicuous, from the numerous, closely-packed, yellow flowers, to the long, slender leaves which are usually deciduous. The flowers do not mature very easily, whilst at this time of the year the number of competing honey-flowers is smaller, and the insect visitants consequently more numerous. On many occasions, the flowers of the willow are so numerous that the wind turns towards the sun and in dancing order, let the upper flowers develop before the lower ones. Hydras frequently appear. + +Trees with verticillate, scale-like leaves: in northern, cold and temperate latitudes. Some in the Polar regions are nearly more than an inch in length, and have a peculiar rhizome (Saxif. hercana, pectina, reticulata). Fossil forms are found in the Cretaceous period. + +*Urea.* Primarily for ornamental trees, as they grow very quickly and are easily propagated by cuttings. The Willows: S. virginiana, S. purpurea; Populus: *P*. deltoides, *P*. nigra; *P*. tremula; *P*. tremuloides; *P*. tremuloides var. *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P*. nigra; *P'. + +340 +DISCOYLEDONES. + +The Cucurbitaceae differ from the ordinary Discocyledons in many important respects which may be briefly summarized thus: The biappendiculate 2-flower has a well-pronounced stylo-cylinder terminated by two stigma, but the cavity of the ovary closes at the base by a thickened wall (fig. 15). The ovules are numerous and ovoidal; these are united by a bridge of cellulose to the stylo-cylinder or summit of the ovary, and are attached to the wall of the cavity by the bursa (above), as well as by the funiculus (below). The mesophyll is composed from the hyphopodar cells at the summit of the nucellus, two primordial nuclei occur within the nucellus, and a large number of primary and secondary cylindrical mass of cells (episporeous tissue) is produced which is surrounded by tapetal cells. The cells of the episporeous tissue correspond to the mother-cells of the ovule, and are derived from the megasporangium. The latter, not less than 16-20 macrospores are formed together with inactive cells which are not crowded together as in the case of other Phoeniogamia. The sexual apparatus is developed in such a manner that each flower contains one pistil. In this species it is subject to change, the corpuscle being accompanied by one or two neighbouring cells. In the majority of the flowers only one pistil is found, but in these it remains as a naked nucellus; while in the fertile macro-spores the endosperm is formed before fertilization, and is then found in all seeds. Antipodal cells are never developed. The macrospore elongate considerably towards the chalazal axis, into which some penetrate. The pollen tubes grow through the chalazal axis, and enter into the nucellus. In passage through the tissue of the nucellus being assisted by the pro- +lusion of the macrospore. Above the centre of the nucellus the pollen- +tube is enclosed in a sheath-like layer of protoplasm, which is finally becoming firmly attached to the macrospore. Although this actual impregnation has not been observed, Trew considers that the endosperm begins to be formed before fertilization. + +Family 3. Querciflorae. + +Trees and shrubs with small, unisexual, monocious flowers, having no perianth or a simple inconspicuous one. The $c$ and $q$ flowers are very different and generally placed in separate inflo- +rencences. The stamens are paired opposite the perianth-leaves, when they are pre- +sent in equal numbers. The $q$-flower is sterile, or has an superior perianth. +The ovary at the base is 2 or 3-(4-) locular with 1 or 2 perianth-leaves. The fruit is a one-seeded nut; endosperm absent; embryo straight. +The inflorescences, which are either compound and mixed (small dichasium in spikes) or simple, are not also termed dichasium; but, +strictly speaking, dichasium is applied to $q$-inflorescences only. +In all Querciflorae the leaves are scattered terminally in 2 rows +simple, and pinnatisected, and with decussated stipules. + +**QUERCIFOLIA.** 341 + +It is worthy of remark that in *Betulaecus*, *Corylaceus* and *Quercus* the ovules, and to some extent the locali of the ovary are not developed till after pollination, so that the development of the pollen-tube proceeds very slowly. The smallness of the ovule, the small size of the stigma, and the abundance of hairs found on many stamens, all point to the fact that the flowers are generally self-pollinated, but that the flowers are generally pollinated before the foliage-leaves are developed, thus preventing the pollen being entangled by the leaves. + +The following account of the structure of these plants is given by other authors united into one order. (It is doubtful whether these two should be retained in the same Quercifoliae, as recent researchers (p. 22) have shown that they differ from the Cupuliferae.) The writer agrees with the Canadenses in the fact that the pollen-tube enters the ovule through the chalazal canal. + +Order 1. **Betulaceae** (Birches). Monocotyledonous, with thick, cylindrical, compound $\zeta$ and $\varphi$ inflorescences (2- or 3-flowered dichasia in a spike with spreading leaves) (Figs. 324, 325, 326). When the perianth in the $\varphi$-flower is completely developed, it is covered by a pair of united leaves, which are placed opposite the 4 stamens (Fig. 325 A). The female flowers are naked; the ovary is bicornuate, with two styles and one ovule enclosed in a single cover-scale (Fig. 325 B). The slender terminal leaves unite with the bracteoles and form a 3-foliate cover-scale, which is not attached to the fruit (Figs. 325 D, 326 B). From this cover-scale arise three lateral branches, each bearing a leaf-like bract (see *Canadense* and *Corylifoliae*). In the bud the leaves are flat. The flowers are deciduous. On flowering the corylids are raised above the ground. Terminal buds are only found on old Abies. + +Fig. 324.—Alnus glutinosa. Branches of Alnus with young leaves and flower-bud. +Alnus glutinosa. A bud with a flower-bud. +Alnus glutinosa. A bud with a flower-bud. + +*Alnus* (Alder) (Figs. 324–326). In the majority of species of $\varphi$-and $\zeta$-cuticles both developed in the buds previous to their flowering, and pass the winter naked and bloom before the leaves expand. $\zeta$-cuticle is a single scale-like cover-scale which is attached to woody and remains attached to the axis, so that its entire cuticle when ripe resembles a small cone (Fig. + +342 + +**DIOCTYLEDONES.** + +324 b). Each cover-scale supports two winged or wingless nuts. +In the native species of Alber the buds are solitary (Fig. 224 t). The bud- +scales are formed by the stipules of the lowest leaves. + +*Betula* (Birch). The *J* catkin, in the native species, appears in +autumn, the 3-flowered in the first year, on leaf-bearing, short- +lived plants. The 3-flowered catkins, divided (Fig. 325 A). The 3- +lobed cover-scales (Fig. 327 a) of the *J* catkin are not +detached from the axis; each cover-scale supports +two winged nuts (b). The stem has hook-like appendages. The young twigs and leaves have aromatic resinous exudation. + +The **Inflorescences** of the *Alber*. + +The Inflorescence of the *Alber*. The *J* catkin is situated in the *J* catkin (Figs. 306 a, 325 A-C). +A 3-flowered dichasium, the flower of which have a 4-partite perianth, the +perianth persistent, with 4 free stamens, and nutlets with numerous filaments. In the *J* catkin (Figs. 325 D, 326 C) a 2-flowered dichasium is found, the middle flower being represented by a single bract (a). + +C. In both instances the inflorescences are **monochasial** (a–c) and the +flowers borne on a common axis (d), one bracteole (g), the other one (h) be- +ing represented by a dotted line; these four bracteoles unite with +the perianth to form a single perianth, thus forming an entire dichasium, to form the 3-lobed +"cone-nut" (Fig. 326 E) which in the *Betula* is called a "catkin." + +The **Inflorescences** of the *Birch.* A 2-flowered dichasium is situated in the *J* catkin (Figs. 325 D, B); only the central flower has bracteoles (i) and nutlets with supporting cover-scale (j), and form a three-lobed calyx (Fig. 327 c). + +A diagram showing the structure of a dioecious plant. +Fig. 325 —Alnus glutinosa: diagram of flowers of *Alnus* and *Betula* catking. +In cover-scale (a) one nutlet is shown; two are represented by dotted lines; and one nutlet is slightly pressed forward from its position in scale (a). +Cover-scale (b) shows two winged nuts. +Cover-scale (c) shows two wingless nuts. +Cover-scale (d) shows one winged nut. +Cover-scale (e) shows one wingless nut. +Cover-scale (f) shows one winged nut. +Cover-scale (g) shows one wingless nut. +Cover-scale (h) shows one wingless nut. +Cover-scale (i) shows one winged nut. +Cover-scale (j) shows one wingless nut. +Cover-scale (k) shows one winged nut. +Cover-scale (l) shows one wingless nut. +Cover-scale (m) shows one winged nut. +Cover-scale (n) shows one wingless nut. +Cover-scale (o) shows one winged nut. +Cover-scale (p) shows one wingless nut. +Cover-scale (q) shows one winged nut. +Cover-scale (r) shows one wingless nut. +Cover-scale (s) shows one winged nut. +Cover-scale (t) shows one wingless nut. +Cover-scale (u) shows one winged nut. +Cover-scale (v) shows one wingless nut. +Cover-scale (w) shows one winged nut. +Cover-scale (x) shows one wingless nut. +Cover-scale (y) shows one winged nut. +Cover-scale (z) shows one wingless nut. + +A diagram showing the structure of a dioecious plant. +Fig. 326 —Alnus glutinosa: diagram of flowers of *Alnus* and *Betula* catking. +In cover-scale (a) two nuts are shown; two are represented by dotted lines; and two nuts are slightly pressed forward from their positions in scales (a). +Cover-scale (b) shows two nuts. +Cover-scale (c) shows two nuts. +Cover-scale (d) shows two nuts. +Cover-scale (e) shows two nuts. +Cover-scale (f) shows two nuts. +Cover-scale (g) shows two nuts. +Cover-scale (h) shows two nuts. +Cover-scale (i) shows two nuts. +Cover-scale (j) shows two nuts. + +A diagram showing the structure of a dioecious plant. +Fig. 327 —Alnus glutinosa: diagram of flowers of *Alnus* and *Betula* catking. +In cover-scale (a) two nuts are shown; two are represented by dotted lines; and two nuts are slightly pressed forward from their positions in scales (a). +Cover-scale (b) shows two nuts. +Cover-scale (c) shows two nuts. + +A diagram showing the structure of a dioecious plant. +Fig. 328 —Alnus glutinosa: diagram of flowers of *Alnus* and *Betula* catking. +In cover-scale (a) two nuts are shown; two are represented by dotted lines; and two nuts are slightly pressed forward from their positions in scales (a). +Cover-scale (b) shows two nuts. +Cover-scale (c) shows two nuts. + +A diagram showing the structure of a dioecious plant. +Fig. 329 —Alnus glutinosa: diagram of flowers of *Alnus* and *Betula* catking. +In cover-scale (a) two nuts are shown; two are represented by dotted lines; and two nuts are slightly pressed forward from their positions in scales (a). +Cover-scale (b) shows two nuts. +Cover-scale (c) shows two nuts. + +A diagram showing the structure of a dioecious plant. +Fig. 330 —Alnus glutinosa: diagram of flowers of *Alnus* and *Betula* catking. +In cover-scale (a) two nuts are shown; two are represented by dotted lines; and two nuts are slightly pressed forward from their positions in scales (a). +Cover-scale (b) shows two nuts. +Cover-scale (c) shows two nuts. + +A diagram showing the structure of a dioecious plant. +Fig. 331 —Alnus glutinosa: diagram of flowers of *Alnus* and *Betula* catking. +In cover-scale (a) two nuts are shown; two are represented by dotted lines; and two nuts are slightly pressed forward from their positions in scales (a). +Cover-scale (b) shows two nuts. +Cover-scale (c) shows two nuts. + +A diagram showing the structure of a dioecious plant. +Fig. 332 —Alnus glutinosa: diagram of flowers of *Alnus* and *Betula* catking. +In cover-scale (a) two nuts are shown; two are represented by dotted lines; and two nuts are slightly pressed forward from their positions in scales (a). +Cover-scale (b) shows two nuts. +Cover-scale (c) shows two nuts. + +A diagram showing the structure of a dioecious plant. +Fig. 333 —Alnus glutinosa: diagram of flowers of *Alnus* and *Betula* catking. +In cover-scale (a) two nuts are shown; two are represented by dotted lines; and two nuts are slightly pressed forward from their positions in scales (a). +Cover-scale (b) shows two nuts. +Cover-scale (c) shows two nuts. + +A diagram showing the structure of a dioecious plant. +Fig. 334 —Alnus glutinosa: diagram of flowers of *Alnus* and *Betula* catking. +In cover-scale (a) two nuts are shown; two are represented by dotted lines; and two nuts are slightly pressed forward from their positions in scales (a). +Cover-scale (b) shows two nuts. +Cover-grade + +QUERCIFOLLE. + +345 + +While the 5-flower exactly resembles that of the Alder, the reduction of the 5-flower, already described in the Alder, is carried further, so that often only two stamens remain, while the other three are suppressed. The petals are also only 2 stamens, these being deeply cleft, while the other 3 are suppressed. + +About 50 species; M. Temp.-Fossil-forms certainly occur in the Oligocene. +Dorothy (1876) gives 100 species, but this number is too large; at present time it is confined to the moors and mountains of N. Europe and N. America and Asia. Wind-pollinated. + +The bark of the Birch contains tannic acid. The bark is used in the preparation of leather boots; whilst its spring sap is very inodorous, and is used in some bays for making a fermented drink. Its external bark is used for cooking, for baskets, etc. + +Fig. 327.—Bulbus serratus: a cone-scale; +from A + +Fig. 328.—Diacmea of dichasium in the 5-flowered D. 5-flowered D. 5-flowered D. 5-flowered D. + +Order 2. Corylaceae (Hazel-族). Monocots. The *c* catkins are long and cylindrical; the *f* flowered are produced singly in the axil of the subtending-leaf (cover-scale); they are naked and formed of a number of divided stamens, which are partly united with the cover-scale; in the Hazel, apparently 8 (Fig. 320 A, B, C), more rarely 6 (Fig. 320 D), or even 4 (Fig. 320 E). The *f* flowers have a central flower (in Fig. 320 F) perianth; in the axil of each cover-scale a 2-flowered dichasium (Fig. 320 D) is present, of which the central flower (in Fig. 320 F) is suppressed. The gynoeceum is bisexual; it consists of two carpels and two stigmas, with two long styles (Fig. 320 D-F); the loculi have I (-) or II (-) (Fig. 320 E). Each single *f* flower and fruit is surrounded by a leaf-like covering, the cupule (husk), which is formed of three floral-leaves (namely, one bract and two bracteoles); in Fig. 320 B, C, a second flower forms its own bracteoles; and B, a, B, the capsule for the right-hand flower, and B, a, B, the capsule for the right-hand. + +Corylus (Hazel-族; Fig. 329). The long, cylindrical *f* catkins pass the winter naked, 2–3 together, on short branches. The very + +344 +DICOTYLEDONES. + +small 5-catkins are enclosed in buds, in which they pass the winter; these buds are situated in the axils of the fallen foliage-leaves, and it is only by their larger size that they may be distinguished from the ordinary foliage-buds. In spring the 5-catkins are easily seen, and are at first green, but soon become brown. The cupule—the "husk"—is tubular, fringed, and envelops the nut. The leaves are alternate and asymmetrical, the external side being larger than the internal; this is connected with the variation, the blade being con- + + +A B C D E F G H I J K L M N O P Q R S T U V W X Y Z + + +Fig. 5th.—Corylus-aurantia. A branch at the time of flowering with 5- and 5-catkins; B 4-flower with subtending-leaf (Caryus) and two bracteoles; C the same without its leaves; D flower with subtending-leaf (Caryus); E young fruit with cupule; F similar one with the cupule opened; G mature 5-catkin; H nut. + +diplicate in the bud; the stipules are deciduous. The bud-scale is formed of stipules, the most internal having a leaf-blade attached to them which is suppressed in the bud. The flowers are perfect, and have no perian- +nium. + +Carpinus (O. betulus, Hornbeam). The 5- and 5-catkins do not appear till the leaves are shooting. The 5-catkin in this + +3 + +**QUESCILOPS.** + +345 + +instance: is also long and cylindrical. The capsule in *C. botulus* is 3-lobed, and to a slight extent only embraces the base of the ribbed nut (Fig. 311); each lobe corresponds to a flaccid-leaf. +Whilst the corollae are placed medianly in *Corolla*, in *Corpus*, on the other hand, they are arranged in two series, one on each side of the axis. The lamina of the leaf is not complemate in the bud, but flat, and folded only along the midrib, so that it is divided into two lobes (Fig. 310). In this form, otherwise the vegetative characters are essentially the same as in the *Irisil*. The corollae are aerial—*Oryza* resembles the Hornbeam, but the cupule contains a single seed (Fig. 312), which is enclosed by a pericarp (Fig. 313). +N. Am., Asia, and Europe; 25 species.—Found forms in the Oligocene. Wind- +pollinated. Urm. As timber (*Corpus* botulus) and firewood. The fruits of *C. cordata* (ordinary Hazel nut) & *C. melosse* (Lambert's nut) & *C. coloma* (Turkey Black) are edible. + + +A diagram showing the structure of a flower of *Corpus* and the dichotomy of the 5-flowered (*P.*) + + + +A view of the Bremontum with cupule. + + +Order 3. **Cupuliferae.** Monocotyledons. The inflorescences make their appearance with the leaves, arising in the axils of the leaves of the same year. A usually cupule furnished externally with scales or bracts, and internally with a single seed or fruit. The cupule in the Corylaceae never encloses more than a simple flower or fruit. +The 2-flower has a united perianth, which is, however, 6-4 partite, and encloses an indefinite number of undivided stamens. The 4- +flowered plant has a united perianth, which is 6-partite (Fig. 32 D, 331); the gynoecium is formed of 2 (or in *Cannabis* 4-6) carpels with a corresponding number of stigmas (Figs. 332 D, H; 334, 335); and the ovary has at the base 3 (-6) loculi (Fig. 331). The fruit is a one-seeded nut (Figs. 332 H, 336). + +The cupule of the Cupuliferae, according to the opinion of Eichler, is formed by united bracteoles (compare Fig. 333, where + +346 +DISOTYLEDONES. +the four valves in the cupule of Castanea are considered as bracteoles of the lateral flowers of the dishiaum); according to another view (see Prantl, in Engler's *Bot. Jahrb.,* viii., 1880), it is a ring-like axial outgrowth independent of the bracteoles of the flower, which is retained on the fruit. In the chestnut and oak only enclose the base of the fruit, but in the Eating, chestnut and Beech the fruit is completely enclosed, and con- + + +A: A young capsule with three lateral flowers. +B: A flower bud. +C: A young capsule with three lateral flowers. +D: A flower bud. +E: A young capsule with three lateral flowers. +F: A young capsule with three lateral flowers. +G: A young capsule with three lateral flowers. +H: A young capsule with three lateral flowers. +I: A young capsule with three lateral flowers. +J: A young capsule with three lateral flowers. +K: A young capsule with three lateral flowers. +L: A young capsule with three lateral flowers. +M: A young capsule with three lateral flowers. +N: A young capsule with three lateral flowers. +O: A young capsule with three lateral flowers. +P: A young capsule with three lateral flowers. +Q: A young capsule with three lateral flowers. +R: A young capsule with three lateral flowers. +S: A young capsule with three lateral flowers. +T: A young capsule with three lateral flowers. +U: A young capsule with three lateral flowers. +V: A young capsule with three lateral flowers. +W: A young capsule with three lateral flowers. +X: A young capsule with three lateral flowers. +Y: A young capsule with three lateral flowers. +Z: A young capsule with three lateral flowers. +AA: A young capsule with three lateral flowers. +AB: A young capsule with three lateral flowers. +AC: A young capsule with three lateral flowers. +AD: A young capsule with three lateral flowers. +AE: A young capsule with three lateral flowers. +AF: A young capsule with three lateral flowers. +AG: A young capsule with three lateral flowers. +AH: A young capsule with three lateral flowers. +AI: A young capsule with three lateral flowers. +AJ: A young capsule with three lateral flowers. +AK: A young capsule with three lateral flowers. +AL: A young capsule with three lateral flowers. +AM: A young capsule with three lateral flowers. +AN: A young capsule with three lateral flowers. +AO: A young capsule with three lateral flowers. +AP: A young capsule with three lateral flowers. +AQ: A young capsule with three lateral flowers. +AR: A young capsule with three lateral flowers. +AS: A young capsule with three lateral flowers. +AT: A young capsule with three lateral flowers. +AU: A young capsule with three lateral flowers. +AV: A young capsule with three lateral flowers. +AW: A young capsule with three lateral flowers. +AX: A young capsule with three lateral flowers. +AY: A young capsule with three lateral flowers. +AZ: A young capsule with three lateral flowers. +BA: A young capsule with three lateral flowers. +BB: A young capsule with three lateral flowers. +BC: A young capsule with three lateral flowers. +BD: A young capsule with three lateral flowers. +BE: A young capsule with three lateral flowers. +BF: A young capsule with three lateral flowers. +BG: A young capsule with three lateral flowers. +BH: A young capsule with three lateral flowers. +BI: A young capsule with three lateral flowers. +BJ: A young capsule with three lateral flowers. +BK: A young capsule with three lateral flowers. +BL: A young capsule with three lateral flowers. + +QUERCZILOR. +347 + +(4), cylindrical, with the 8 at the base and the 5 at the top; or some are entirely 5 and composed of small dichasia. The capsule (C, E') is 4-ruled, provided with spines, and entirely envelops the 3 nuts; it is already developed at the time of flowering.--5-dwarfs are usually found in the woods, and are very common in the principal parishes, most frequently consisting of 6 leaves in two wheels (Fig. 832 D), and a large number of stamens. 2-dwarfs are most frequently born in 3-leaved dichasia, which are often very large, and have a single nut in each wheel. The flowers are showy, according to which the 6 bracteoles (a'--p') of the two lateral flowers are thick and united into a single 4-ruled, several cupule, which surrounds the 3 nuts, and is covered by the perianth. The perianth is composed of several harices.--carpels in two wheels.--The leaves in the vertical shoots have a divergence of $E_1$, $E_2$ on the horizontal shoots they are alternate. + +Fucus (Beach). The f-catkins are pendulous, capitules; the f-flowers have an obliquely bell-shaped, fringed perianth, with 0-20 stamens. 2-catkins erect, 2-flowered, borne singly in the axil of foliage-leaves of the same year; the f-flower has a gynoeceum formed of 3 carpels, bearing an epigynous, 6-leaved perianth (Fig. 354). In this genus the dichasia is only 2-flowered, the central one being always sterile. The fruit is a small nut, or a pair of triangular nuts ("mast"). All the shoots have the leaves arranged in two rows; the rows are on the underleaf, being only about 90 centimeters from each other; those on the upper leaf are about 1 meter apart. The leaves pale. The bud-scale is stipulate without lamina; in verticillate laminae are folded along the lateral ribs, the upper lateral portion being the largest (as in Horn-bush). The leaves are simple, entire, and alternate. The flowers are aerial, large, and reniform. 4 species (Europe, Japan, N. Am.)--Nephrolepis (S. Am., New Zealand, S. Aust.). + +Quercus (Oak; Fig. 355). Catkins simple. f-catkins long, thin; three or four flowered; perianth with a single nut in each carpus; the perianth is composed of several harices.--The f-flower has similar construction to that of the Chasmat. The + +Fig. 353.--Diagram of the capitule of Conostylis. +Fig. 354.--Female flower of Fucus (marg.). + +348 + +DICTYOTYLONSE. + +† Ocatnik has not more than 5 flowers (single-flowered diclinia, in which only the central flower is developed). The scales on the cupules are no double-leaf structures in this case also. According to another theory, the scales are hair- +structures, but according to the first theory they are leaf-like, and are arranged in ascending, but really in descending order. The rim of the cupule gradually expands. In the Y-flower (Fig. 35b) the incisil of the gynoecium, together with the ovary, is divided into two parts by a median groove. The petals are often very large, and may have a divergence of ; the leavemost leaves on the shoots are reduced to stipules which serve as the bud-scales (5 rows). The laminae are conduplicate, as in *Corylus* (Fig. 36a), and are usually deciduous. The stipules are rarely and remain underground. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 300 species. —*Pannus* (100 species). + +300 species, in temperate regions. The following genera are found in Europe and N. America. +*Arctostaphylos* (10 species), *Arbutus* (2 species), *Betula* (10 species), *Fagus* (2 species), *Fagus sylvatica*, in Europe; it is a most important forest tree (in Denmark the tree grows up to 100 feet high); the northern limit of its occur- +sion in Norway is at 67° N.L.; its southern boundary is near 50° N.L., in Alpenaum; in a zig-zag line through Lüneburg, south of Kingsberg, in Prussia, to- +wards the Crimea. According to Steenstrup and Tangier, the Beach did not +make its appearance in Denmark until a comparatively recent time, the Oak +short before the last glaciation. The following species of Beech are found in N. +America and Japan. Several species of *Nectria* occur in the South West +of S. America, and in the colder regions of the North Pole. The +oak grows well in Japan; it is found in the Western Asia, N. America, +and the mountains of Mexico. Evergreen species are found in Tropical Asia, +Himalaya, and China. The following are known: *Quercus* (12 species), +species of Oak (*Q. robur*), of which there are three varieties (*Q. pedunculata, +ferruginea, sessilifolia*). The Baking-chestnut is found in the South of Europe, +but is considered rare in England and France; it is found in Italy. + +The wood of these trees is very useful as timber. The wood of *Q. tectoria* +has a yellow colouring matter (Quercitron-wood). The bark of the Oak contains +a large amount of tannin; it is used for tanning purposes; some other trees, +also the cupules of *Q. robinae*, *quillpe*, and others from the Eastern +Mediterranean, are used under the name of *Vallonia*. The Cork-oak +(*Q. suber*: S.W. Europe) is the most important tree from which cork is obtained, + +Fig. 35b.—Quercus: A flower in its cupule +(cease): if longitudinal section through A, +showing ovary, pericarp, and laminae. + +Fig. 36a.—Tree of Quercus. + +JUGLANDIFORUM: 349 + +its bark being very hardy developed and stripped for work. Gall-nuts are found on many species; those of Q. fraxinifera, var. infectoria (Eusierum Mallorcanum) are official, and likewise the fruits (acorns) and the bark of Quercus pedunculata and willow-olive. Oil is obtained from the Bessi- **man**. The nuts of the Chestnut tree are edible. + +Family 4. Juglandiforum. +This family resembles the Querciflorum in the oak-like inflorescence, the imperfect, *unisexual* flowers, the epigynous perianth and the woody shoots with scattered leaves, etc., though it is in other respects very dissimilar; one point of difference is the presence of a single ovary in the female flower, which is not found in the structure of the gynoecium, which is formed of two carpels with one loculus and has one basal, orthotropic and erect ovule. + +Fig. 307. — Juglinae regula: A—flower seen from below with heart (acorn-only) (1); b—female flower with two sepals, two petals, two stamens and a single ovary (2); c—diagram of A; d—flower with bracts, the bracteoles united with the corolla; e—female flower with two sepals, two petals, two stamens and a single ovary (3); f—diagram of C; g—female flower with two sepals, two petals, two stamens and a single ovary (4); h—diagram of D; i—female flower with two sepals, two petals, two stamens and a single ovary (5); j—diagram of E; k—female flower with two sepals, two petals, two stamens and a single ovary (6); l—diagram of F; m—female flower with two sepals, two petals, two stamens and a single ovary (7); n—diagram of G; o—female flower with two sepals, two petals, two stamens and a single ovary (8); p—diagram of H; q—female flower with two sepals, two petals, two stamens and a single ovary (9); r—diagram of I; s—female flower with two sepals, two petals, two stamens and a single ovary (10). + +Order 1. Juglandaceae (Walnuts). Leaves scabrous, imparipinnate, rich in aromatic compounds. Stipules absent. Flowers uni- +sexual or perfect; the male flowers with three sepals, three petals and six stamens; the naked branches of the previous year cylindrical; pendulous, many-flowered; the two bracteoles and the 2–4-leaved perianth of the Z.—flower unite with the subtending bract; the Z.—flower has indefinite stamens (6–20 in Juglinae; Fig. 307 A–D). The Z.—catkins are terminal, gene- +rally on branches of the same year few-flowered (Fig. 307 F); the + +350 + +DECOTYLEDONES. + +9-flowered have a superior, 4-leaved perianth, a bispinate cymen- +num, two styles with stigma on the internal surface. The ovary, bracteoles and bract all unite together (Fig. 337 E). The fruit is generally a green or black drupe,2 whose flesh (outer soft portion) in Carpea and Juglans ripens more or less irregularly, and from the stone (Fig. 337 F) and by several seeds, few partition walls into several complete com- +partments, so that the two large cotyledons become lobed and inclined to fit like a coat pocket. The seed-coat is thin, smooth, and often papery, or exospermous and covered with a thin testa. --The leaf scars are large and conoid with 3 groups of vascular bundles. The first in Juglans and Pterocarya is shifted to the upper side of the leaf-stalk, while the second is on the lower side of the leaf-stalk into a valve; the cotyledons remain underground. In Juglans regia a long row of accessory buds is found on the lowest internodes (epipodophy) +above this row of buds, which are very similar to those of the common walnut, +and protandrous examples of Juglans regia occur.--35 species, mostly in tem- +perate North America, are cultivated for their nuts. Juglans regia is native to +Hickey from North American species of Carpea. The oil-containing seeds of +several species are edible. Pterocarya and others are cultivated as ornamental plants. + +Order 2. Myricaceae. To this order belong shrubs or trees which have penicillate, simple, at least lobed or pinnatifoliate leaves, with or without stipules. The flowers are sessile or pedicellate, in a cyme +(Fig. 338 A). The flowers, situated in catkin-like spikes, are unisexual and naked, and supported by scale-like floral-leaves. +-Flower: 4–6 (-16) stamens with short filaments; -1: generally situated on one side of the spike; -2: opposite to the stamens; -3: stigma; +stamens, and unite with the bracteoles, which form wing-like outgrowths on the ripe drupe as in Pterocarya in the Juglandaceae (Fig. 338). Oxydendron flexu (Fig. 338 D) --Myrica: Comptonia. + +Fig. 338.—Species plate: a young fruit; b the bracteole with inconspicua glaada; c longitudinal section of fruit. + +--- +1 The fruit of the Walnut is then a false fruit; and the term drupe must therefore not be used in the same sense as in the Rosaceae. + +**Urticifolie.** 351 + +40 species; Temporaria.—*Urtica* palata (Swiss-gale, Bog-mastix) has been used in the preparation of beer (sweet-willow bark) on account of its riches essential oil. *M. cerulea* (N. America) and species from the Cape, *M. quercifolia* and others, form wax on the fruit which is used in the preparation of candies. + +Family 5. Urticifolie. + +The flowers are regular, hypogynous, nearly always unisexual, small and insignificant, with simple, green perianth of 4-5 leaves. +Stamens 5-6, placed opposite the leaves of the perianth. Ovary funicellate, sessile, or with a short pedicel, with one ovule (Fig. 340). The fruit is a nut, rarely a drupe, with one seed, generally endocarpous. The Nettles are the sole order in the family which has only one carpel (1 stigma); this turns the posterior side to the upper surface of the fruit (Fig. 341), while in all other families only is fercula (Fig. 342) except in a few Ulmaceae and Moraceae, stipule-like appendages being present at the base of the leaves. + +The majority are trees or shrubs with petiolated leaves, stipule-like appendages at the base of the leaves. + +The flowers are very often crowded together in the inflorescence, which is rarely catkin-like. Peculiar aggregations of fruits are found in some orders. *Latius* and tough leaf, which is used techni- +cally as a medicine, is a common plant in the epidermis of many species of *Ficus*, *Urtica*, and others. *Wend* or *selfpollination* is most common, as in the Quercifoliae and Juglansideae. +The flowers are usually perfect, but sometimes male on one side and female on the other; when ripe straminea themselves entirely and elastically, and thus small clouds of pollen grains are ejected with considerable violence on to the stigmas, which are then covered with bracts like hairs (Fig. 341). The formation of seeds does not take place. + +Order 1. Ulmaceae (Elms)—Trees or shrubs without latex, +simple leaves, alternate or opposite (Glabrous), or glabrous (the imparipinnate leaves having two axils being the largest), simple or pinnate-nerved, dentate, hispid; stipules deciduous. +In opposition to the other Nettle-like plants the flowers are often 2 with a united corolla axillary, generally 4-5-cleft or cleft-petals persistent, and a calyx opening to leave number of petals or stamens. The gymnoecium has two carpels (2 stigmas), generally one fertile and one sterile. Fruits one-seeded (gut or drupe). Embryo without albumen. + +A. ULME. The fruit is a winged nut (Fig. 330), the embryo straight, without endocarpus. Authors extreme—*Ulmus* (Elm). + +1 The pollen-tube in Ulmus does not enter the ovule through the microspore. +W. R. +A.A + +352 + +DICOTYLEDONES. + +The flowers are situated in inflorescences which develop from the lower buds of the shoot of the preceding year. The lowest bud-scales are erect, the uppermost support either solitary flowers, or small, dichasial or uniparied scapoid inflorescences. The pedicel is petiolar, but soon after its insertion the petiole abscises quickly falls off, and the upper lateral bud continues the growth of the flower-bud until it is placed before the leaf-bud open. The flowers are wind-pollinated and have no honey. For several genera have been found in the Oligocene. + +20 species; North: 17 (species with one stamens), South: 3 (species with two stamens). The Cork-bark (T. oleifera) has a rather thick bark which is used for medicinal purposes. The last is used as Lime-bark. + +B. Cacumen. The fruit is a drop, the entire calyx, with folded or rolled up corollae, with or without endo- +spores, or with a single seed. The +flowers are borne on a shoot of the +same year. *Florina* (N. American); *Cacumen* (about 114 species, especially N. Temp.). + +For, 383.—Elusa compacta, flower +with conspicuously shortened gynoeceum; +A. Sperma, flower with conspicuous +compacta, fruit opened in front to show +the seed position; A. corymbosum of the +botanica, whose bocula is aborted. +Order 2 Urticeae (Nettles).—The majority of spe- +cies are herbs with simple, stipu- +lated leaves, and have no hair; but +stinging hairs abundant. The flowers (Fig. 346) are gen- +erally 2-merous and arranged in clusters, which are united into +(1+2) by a common base, or in a few cases generally united, green leaves; +the 4 (2+2) sepals are opposite to each other at the base of the flower, +are bent towards the base and throw themselves elastically towards the outside. The gynoeceum has one style and one stigma +(capitate or bract-like; Fig. 341); the stamens are usually opposite to each other, +orthogonally inserted on the pistil (members of this family have inverted +or curved ovaries). Fruit, a nut or drupe. *Urtica* present +(1 in Urtica very little), ally. Embryo straight. The strong nectaries are +attached to the base of the calyx, which breaks off in an oblique direction and allows the pollen-cells to be forced out. In many tropical species this is so strong that it may produce partial parietal placentation in the rudiment of an ovary in the *D*. *Flower* (Fig. 343 d). The stamens in the *D*. *Flower* differ from those of the *D* in having two the + +CHITONIFLORE. + +Internal leaves generally much larger and enveloping the fruit (Fig. 30.) ; it +often happens that all the perianth-leaves are united to form a gamophyllous envelope. 5-flowers may occur among the others. The inflorescence among +the leaves is usually a panicle, but sometimes a raceme. The perianth is a unilateral +scorpioid cyms by the development of the bud of the 2nd bractule. In +Paritioria they are more pressed together, and the floral-javens at the same stage are more closely united than in Utricula. The flowers are 5-angled. As a +rule, not only in this order but also in those related to it, a small vegetative +stem is situated in the axil of the foliage-leaf, and this bears an inflorescence +on its upper side. + +Utrica (Netticle) has opposite leaves with distinct stipules and +stinging hairs. The perianth-leaves of the 2-flower are free (Fig. 340.)—Paritioria (Pelletory) has scattered leaves without +any stipules, or both stipules and stinging hairs are absent. The 7-perianths +is 4-toothed, flanks, or both stipulated.—Utrica is a tropical genus with trimer- +cia, symmorphic; P. diversa, the perianth perianths had been much larger than + +A diagram showing the structure of a flower. +Fig. 340.-Diagram of 4- and 5- +flowers of Utrica divisa. + +For. 341.—Paritioria diversa, hermaphrodite. +The flowers are 5-angled, and have no inflorescence +ment of the male stage; the latter have no falcon +cut, but the anterior have not yet developed. + +the two others, and more or less hood shaped.—The flower of Paritioria is the +most reduced; the 5-flower has only one leaf-like bract. In Utrica the 5- +flowers have a one-sided, tongue-like perianth (Fig.). Funicella. +Wend.-FELDSTEIN: The polies is shot out of the anthers, when they spring +from their sheath, which is formed by the base of the petals. The stigma is prophy- +nous (Fig. 341). +380 species : chiefly in the Tropics, although few species which occur +in temperate regions are by a large number of individuals.—Utric. +The best of the native species Utrica divisa and some of U. cernuaeanum (Cernuaeanum), which grows on sand-dunes in China, and U. hirsuta (from Sunda, +China), and odora, is used in the manufacture of muslin. + +Order 3. Moraceae (Mulberries). Nearly all trees or +shrubs, seldom herbs, generally with latex. The leaves are scat- +tered, and not infrequently lobed. Flowers are bisexual or unisexual +(monoecious), and often showy; they are in catkins or panicles like +comparatively inflorescences. +Perianth-lavens 2-6, generally 4, with an equal number of stamens opposite to them, as in the Netticles. The + +354 + +354 + +**Eriotyledoxus.** + +ovary is 1- sessile 2-lobular, and has 2 stigmas (it is thus formed from 2 carpels) seldom only one style with one stigma. One ovule in each locule, more or less curved, and *pseudoul*; micro- +pyle directed upwards. Fruit usually a drupe. The embryo is +generally covered inside the fleshy endocarp, or it is exochospermous. + +A. **Morus alba** Linn. (Mulberry). The leaves are very +folded in the bud - *Morus* (Fig. 342-344). Monocious. +The inflorescence are catkin-like in appearance, but in reality +composed of many flowers. The flowers are similar to those +of the Nettle, with 2 carpels in the bud (Fig. 342), 2 + 1, +and stamens 2 + 2 (Fig. 342), in the $q$, periand 2 + 2, and 2 +carpels in regular alternation. The small drupes are enveloped +by the periand, which eventually becomes fibrous, and as all the +flowers on the axis very accurately fit together, the collection of + +Morus alba +**Fig. 342—Morus alba** +fruit is formed, which we call a Mulberry (Fig. 344). The leaves are folded in the bud, and have small stipules. The following are +allied to *Morus* - *Maclura*, Broussonetia (the Paper-mulberry tree) which has gynodioecy. + +*Dorstenia* presents an interesting transitional form to the Fig in its flat, +open, and in some cases even closed state, because on which the $f$ and $v$ +leaves appear as two leaves. In fact, indications of a second leaf are found in certain Nettles, the symmetrical axis of the dichasia becoming flatty +expanded. The fruits are 1- seeded, but nevertheless, spring open and eject +their seeds. + +B. **Autocarpus**. Filaments straight in the bud; foliage- +leaves with conuate lobule. An interpetalate leaf-shoots (Corolla) +are produced by the axillary buds of the young leaves which +cover the younger leaves as a hood. It falls off as the leaf expands, and leaves a ring-like scar on the stem - *Ficus* (the +Fig). The inflorescence (the so-called syconus) has a pear- + +355 + +shaped, flaky, but hollow axis, on the interior surface of which the flowers are situated (Fig. 345). It is a kind of capitulum, with a hollow receptacle, whose "involucral" leaves close over the entrance to the interior; it is not, however, a simple capitulum, but a coalescence of cymose inflorescences. The edible parts are the fruits, which are drupes, with thin flesh. + +The fruit of the fig is a berry, which has a 2- divided perianth, 1-2 (-6) stamens; the 2-flower has an oblique ovary. The fruits are drupes, with thin flesh. +—Many species have sessile fruits, and many others pedunculate on trees. +Ficus carica (Fig. 346), the fig tree, is affected by a small insect, called *Carpinus* (*L.),* which lays its eggs in the figs, and hence carries the pollen away. +Insects are often found in the figs, and they are usually considered customary to hang infected with figs on the branches of cultivated ones, so that they may pollinate them. This is not always true; for when they have emerged, could immediately effect the pollination (impollination). Ficus carica is visited by two kinds of insects: one kind of *Drosophila* (Fig. 347), which is common to all kinds of *Drosophila*, besides the *D.*-flowers. One kind has a short style and no stigma, +neither can it fertilize any flower; the other has a long style and stigma, and can fertilize any flower; but the wasps cannot reach their ovaries because they are too long. Moreover, two kinds of plants of *Ficus carica*: *2-plants*, which have only seed- +stalks; and *1-plants* (called "Capriformi"), which bear insoluble fruits, and have 2-flowers. + +**[Captioned figure]** +Fig. 345.—A fig in longitudinal section. + +**[Captioned figure]** +Fig. 346.—A fig in longitudinal section. + +**[Captioned figure]** +Fig. 347.—A fig in longitudinal section. + +Naples, three crepe of middle figs each year, viz. Massae (April), Pro- +nese (May), and Caprini (June). The first two are very small, but the third +the first figs being almost entirely *2-plants* and the last having few *2-plants*. +Each crep produces a new fig every year; and this is repeated until the crep +is exhausted. The female-wasp lays one egg in each flower, with the result that +the flower develops into a kind of gall. The mother-wasp dies within the Fig. +The male-wasp hatches out from his egg; he flies about seeking females among +the female wasps and impregnates them; the female wasps then escape from +the Fig, those in the Prodelgare carrying pollen away with them as they pass out. +The Prodelgare is a kind of tree which grows in Italy; it is similar to the fig tree, +similarly has three creps in the year. Furi di fiori, Pedaniati, Cenarii. +The wasps entering these Figs, are unable to lay their eggs in the ovary, but, +nevertheless, they effect cross-pollination on entering the Pedaniati, which +bear quite much. + +Fig. 345 - A fig in longitudinal section. +Fig. 346 - A fig in longitudinal section. +Fig. 347 - A fig in longitudinal section. + +356 +356 + +**Dactylodendron.** + +The flowers of *Brownea* is the most relished. The perianth is wanting, and the 5-merous has only 1 stamen. *Ceropogon* (Trumpet-tree), in S. Am., has its petals divided into lobes; these are inhaled by ants, which feed upon small food particles adhering to them. The leaves are alternate, simple, entire, and pinnate, often sheathed, fringed or lobed, and sometimes with white felted hairs. They serve as food for *Brugmansia* (the Saffron). *Rourea*: *Camellia*. About 200 species of this genus are found in tropical Asia and Australia. *Murraya* (Mr. mille, from India, China). *Mullerita* is cultivated for the sake of its leaves, which are used in the preparation of tea. *Murraya* (Mr. mille) is cultivated for its fruits, which are used for the official Mullerite juice. The oleander Fig-tree (Ficus carica) is from the Mediterranean. The fruit of the *Ceropogon* is eaten by the ants, and the *Ceropogon* fruit tree (Annona sawi) and the Jack (L. reticulatus) have their home in the South Sea Islands, and are cultivated in tropical countries. The Broad-fruited Fig (Ficus carica) is a native of India, and has a peculiar influence on those whose hair and lanugo become silky and unite into one continuous mass, together with the skin, which is also silky. The mulberry (Ficus carica) is a native of India, and is used as a common house-plant, and of Canavalia ensiformis (Am.) as raw material of India-rubber. + +The mulberry juice of India-rubber trees (Ficus carica) is a stimulant and antispasmodic; it is also tonic; the Umaran, at Java! it is a strong poison. The best of the Paper-Mulberry tree (Ficus bengalensis), Eastern Asia is used for paper; it is very hard; it is hung upside down (Gossypium hirsutum), which lives upon *Ficus bengalensis* and F. religiosa (the Bo-tree, sacred to Buddha), E. India. The wood of *Medina serrata* (Am.) has a yellow odor, and is known as yellow Brazilian wood. + +Order 4. **Cannabaceae.** The plants which belong to this order are aromatic herbs, either annuals or perennials, without leaves. Leaves pubescent, or more or less divided, stipulate, and with free, or united stamens; ovary superior; ovules in panicles, formed of dichasiae, passing over into uniporous scorpioid cymes. They differ from the Nettles, particularly from the 5-leaved perennials of the genus *Urtica*, by having 2-merous flowers (Fig. 346-351) with filaments erect in the bud, and in the 2-flowered by the small, entire, cup-like perianth; by having two styles or one divided into two, with two stigmae and a pistillate ovary. The sepals of the embryo are curved (Hemp, Fig. 352); the fruit is a nut; but only one style is curved (Hemp, Fig. 353); or rather (Hemp, Fig. 350), without endosperm. + + +A B C D E F G H I J K L M N O P Q R S T U V W X Y Z + + +Fig. 346.-Diagram of male and female flowers of the Hop hemp: A-B-C-D-E-F-G-H-I-J-K-L-M-N-O-P-Q-R-S-T-U-V-W-X-Y-Z. +A-B-C-D-E-F-G-H-I-J-K-L-M-N-O-P-Q-R-S-T-U-V-W-X-Y-Z + + +**UTICIFOLIE.** + +Only 2 genera with this specific (Aristol.), of which two are culti- +vated. — *Humulus lupulus* (Hop, Figs. 347-349) is a twining, +perennial plant, twisting to the right, with opposite, palmilobed, +rough leaves, and large, interpetiolar stipules. The 2-flowers are situated in closely-flowered corymbs, compactly-converging +towards the axis, large, their imbricate floral-bears (Fig. +348) which bear the yellow, glandular hairs, containing lupulin. + +357 + +Figs. 347-348.—*Humulus Lupulus.* 347, twining stem ; 348, branch with corymb. + +This inflorescence is made up as follows.—The most external floral-bears are +situated in pairs, and are the persistent stipules of a leaf, the buds of which +have been shed. The central axis is furnished with a pair of bracts, and supports +4 (2-6) flowers in a double uniparous cyme, whose central axis does +not develop into a flower. The lateral branches of the cyme are the +persistent stipules, at maturity, very large, spike-like, and, together +with the stipules, produce a cone-like appearance. + +*Cannabis sativa* (Hemp, Figs. 350-353) is an East Indian herb, +with palmilobed leaves, and differs from the Hop in being annual, + +358 + +358 + +DISCOTYLEDONES. + +erect, and in having its leaves opposite at the base and scattered above. The *Q.*-inflorescence is not cone-like as in the Hop, but the flowers are similar in construction. The main difference is in the *Q.*-flower sheath, which is long and narrow in the Hop, and is in the Discotyledon opening into a leaf-bearing shoot which on each side bears only one flower. This is the chief fact that the plants are not so strongly developed. + +The "Hop" (the female inflorescence) are used in brewing, and the seeds contain a bitter principle, glands which contain lupulin. The Indian variety of Cannabis sativa contains an abundance of glandular resin, which is used in medicine and are official. The best of the stems of the Hemp is also used and the fat oil is used in Oriental countries the entire plant is used as a refreshing drink (hashish), the narcotic matter being found in the glandular hairs. + + +A - 200. Cannabis sativa; 201. q-flower; 202. q-flower; 203. q-flower, entire and longitudinal section; 204. fruit in longitudinal section. +B - 250. Cannabis sativa; 251. q-flower; 252. q-flower, entire and longitudinal section; 253. fruit in longitudinal section. +C - 350. Discotyledon. +D - 350. Discotyledon. +E - 350. Discotyledon. +F - 350. Discotyledon. +G - 350. Discotyledon. +H - 350. Discotyledon. +I - 350. Discotyledon. +J - 350. Discotyledon. +K - 350. Discotyledon. +L - 350. Discotyledon. +M - 350. Discotyledon. +N - 350. Discotyledon. +O - 350. Discotyledon. +P - 350. Discotyledon. +Q - 350. Discotyledon. +R - 350. Discotyledon. +S - 350. Discotyledon. +T - 350. Discotyledon. +U - 350. Discotyledon. +V - 350. Discotyledon. +W - 350. Discotyledon. +X - 350. Discotyledon. +Y - 350. Discotyledon. +Z - 350. Discotyledon. +AA - 350. Discotyledon. +BB - 350. Discotyledon. +CC - 350. Discotyledon. +DD - 350. Discotyledon. +EE - 350. Discotyledon. +FF - 350. Discotyledon. +GG - 350. Discotyledon. +HH - 350. Discotyledon. +II - 350. Discotyledon. +JJ - 350. Discotyledon. +KK - 350. Discotyledon. +LL - 350. Discotyledon. +MM - 350. Discotyledon. +NN - 350. Discotyledon. +OO - 350. Discotyledon. +PP - 350. Discotyledon. +QQ - 350. Discotyledon. +RR - 350. Discotyledon. +SS - 350. Discotyledon. +TT - 350. Discotyledon. +UU - 350. Discotyledon. +VV - 350. Discotyledon. +WW - 350. Discotyledon. +XX - 350. Discotyledon. +YY - 350. Discotyledon. +ZZ - 350. Discotyledon. + +Family 6. Polygoniaceae. + +This family is on one side closely allied to the *Urticaceae* by its solitary, basal, vertical, and straight ovule, and by the conical ocrea which envelops the younger leaves in the bud, similar charne- + +POLYGOSISFLORE. 359 + +ters being present in the Urticales. On the other side it is related to the Curvarembryum. The flowers are small, often *trimerous*, regular and slightly perigynous (in Chloranthaceae, if they properly belong to this family, and *Buxus*), more or less epigynous. Symmetry is usually 5-merous, but in some cases it is 4-merous, or even 6-merous, or occasionally a single fruit, one-seeded berry, nut or drupe. The leaves are generally scattered. + +Order. *Polygonoaceae*. The majority are herbaceous plants with round, sessile, pointed leaves, scatellar leaves and oars, that is a membranous, tubular, ligular or stipular structure *inside* the base of the leaf, which clasps the stem and axillary bud ; the edges of the lamina are rolled backwards in the bud. The flowers are usually 5-merous, sometimes 4-merous or slightly perigynous, with inconspicuous, simple, green or white perianth ; 5-6 free segments ; stamens 3–5(0) sometimes arranged in two series ; gynoeceum : *one basal*, straight (orthotrope) ovule, 2–3 free styles. The fruit is a 2–3-angled nut ; the embryo, with mesocarp and endosperm ; the seed curved (Fig. 355 H), often asymmetrical. --The inflorescences are com- posed, and generally branch from the axis below the flower ; the lateral partial-inflorescences become collateral, usually with a few flowers. --The fruit is formed by the two bracteoles united in a mem- branous tube ; in *Rhamnus* and *Rhamnus* there is only one such tube. + +*Rhamnus* (Rubber). Fig. 354 A) has a 6-leaved, petiolated perianth (P + 3 + 3) and 9 stamens (A + B + C). The 5-circled nut is not enclosed by the perianth. + +*Rumex* (Dock). Fig. 354 B) has 6 stamens (P + 3 + 3); the perianth is 6-leaved (P + R + S), green or red, and the triangular nut is en- closed by the perianth. The perianth remains on the plant for a long time and continue to grow after flowering. These perianth-leaves often have hairs on their outer surface. These following are monoeious : E = axile pistillate flower. + +*Polygonum* (Knot-grass, Figs. 354 C, D; 355.). The petiolate perianth is most frequently 5-merous (4 spines) ; 5–8 stamens. The nut is triangular (Fig. 354 C, D); or lenticular (Fig. 354 D). + +A diagram of Rhinum ; B of Polygonum ; C of Polygonum ; D of Polygonum. +Fig. 354 + +360 + +DIOTETLEONES. + +There are two whorls of stamens, the external with introve, and the internal with exrove anthora. The gymnosperm is often bi-carpellate (Fig. 354 D). + +The flowers of the genus *Pterostegia* (Fig. 354 A) are of the monochlamydean type. *Pterostegia* has a perfectly monochlamydean flower with 3 trimerous whorls. *Rheum* likewise, but here the external staminal whorl is doubled (Fig. 354 C). On the other hand, *Eucalyptus* (Fig. 354 B) is a diclinous flower, with 2 stigmas. *Rumex* has a rheos- flower with the suppression of the internal whorl of stamens (Fig. 354 B); *Eucalyptus* is a diclinous rumex. *Polypogon*, to which *Coriaria*, *Melodorum* and others are related, differs from *Rheum* + +A branch with flower and fruit (cont. cont.) +A flower; C the stem in longitudinal section; D anterior and posterior view of stamens; E gymnosperm; F front view of stamens; G cross-section of stamens showing the curved corollae embedded in the endocarps; H the embryo. +chiefly in having one of the leaves, which is the latter taken part in the formation of the ovary, and in having only one carpel (the other being either aborted or reduced to free members), and several or all the stamens in the inner whorl become suppressed.—The perianth in *Coriaria* and *Melodorum* is more or less persistent, but in *Melochia* it is deciduous. *Melochia* nodiflora has flat branches with radiimentary bracts; sometimes branches with normal, arrow-shaped leaves are found. *atrophiza.* + +354 + +A branch with flower and fruit (cont. cont.) +A flower; C the stem in longitudinal section; D anterior and posterior view of stamens; E gymnosperm; F front view of stamens; G cross-section of stamens showing the curved corollae embedded in the endocarps; H the embryo. +chiefly in having one of the leaves, which is the latter taken part in the formation of the ovary, and in having only one carpel (the other being either aborted or reduced to free members), and several or all the stamens in the inner whorl become suppressed.—The perianth in *Coriaria* and *Melodorum* is more or less persistent, but in *Melochia* it is deciduous. *Melochia* nodiflora has flat branches with radiimentary bracts; sometimes branches with normal, arrow-shaped leaves are found. *atrophiza.* + +POLYGONOPLEURA + +361 + +**FOLIATION.** *Rhamnus* is said pollinated, the stigmae are therefore large and brachy-like (indicated in fig. 504). *Rhamnus* and *Polygona* are insect-pollinated and have therefore capitulate stigmas, etc.; but heavy-glands are situated at the base of the stigmas, which are then sessile. The stigmas of *Polygona* are different from those of *Rhamnus*. Some species of *Polygona* are self-pollinated; *Buckwheat* (*P. fagopyrum*) is dimorphic and has long-styled and short-styled flowers (figs. 505, 506). *Pol. historiae* is prostan- +dinate. + +About 750 species, most of which are found in the temperate regions of the Northern Hemisphere, belong to this genus. They are distributed into the Arctic regions (Oxyria, *Eriogonum*), Eurasia and North America. *Cucurbita*, *Coccoloba*, *Triglochin*. *Rhamnus* is Central Asiatic. The thick rhizomes of R. +officinale (fig. 507) are used in medicine. The seeds of *Polygona* are utilized by man; R. waddellii and rhabdophyllum, are used in veterinary medicine. The following are cultivated as culinary plants for the sake of their leaves—*Rhamnus*, *Cucurbita*, *Coccoloba*, *Triglochin*. In addition to these, several species of *Polygona* (*P. hydraparum* and others) have a sharp, pungent taste. “Buckwheat” is the mainly fruit of *Polygona* papuanum (Central Asia) and *P. fagopyrum* (Europe). The leaves of *Cucurbita*, *Cucurbita*, *Aganosma* is an ornamental plant—Califorians in sandy soil and some desert. + +Order 2. Piperaceae (Peppers). Shrubs or herbs, often with nodules, jointed stem; leaves simple, entire, often with curved veins; stipules wanting (Piperaceae) or intrapetiolate and cap- +like, often enclosing the terminal buds (Piper). The flowers are in spikes with fewish axes (sub-club), solitaries in racemes, the outer ones are crowded and are $\frac{1}{2}$ unisexual, always small, naked and without bracteoles; generally stamens 3+3, and gynoecium 3, but the male organs may be reduced to one or two; ovary usually 1-celled. + +The flowers are situated in the axils of the small, generally shield-like floral-leaves. The ovary is always unilocular and has one or two cells; the fruit is oval or ovoid. Fruits a berry or drupe. Both endosperm and perisperm are present, the latter being especially well developed (fig. 359). + +*Piper*: generally shrubs with scattered leaves, and terminal + + +A diagram showing the structure of a flower in the family Piperaceae. + + +Fig. 505.—Flower of *Polygona fagopyrum* in longitudinal section: 1, long-styled; 2, +short-styled; a, the anthers; b, the stigma. + + +362 +DECTOTLEDONES. +inflorescences which are crowded to one side by the development of the highest lateral bud, so that they are situated opposite the leaves (Fig. 357). Many species have stems with an abnormal anatomical structure. --Pepomisum: chiefly succulent herbs, often epiphytes, but opposite or verticaliate leaves having aquane bases on the stem. + +The group Lactaria (considered by some as six order, and perhaps representing a more original type) has 8-4 carpels with many ovules. *Lactaria* stands the highest with regular 8-merous perianth, 8-+ stamens and 3 carpels, which are + +Fig. 357.--Piper ssp. ; branch with fruit (1) +united at the base. Fruit a capsule with several scales. (It has one species from the island of Juan Fernández, and is also placed in an order of its own, *Lactaridaceae*, by some.) The flowers are usually solitary, sessile, with 8-4 petals; most frequently 8 stamens, and 4 carpels, free or united at the base, each with 8-4 ovules. The ovary is usually subglobose or ovoid, sometimes prolonged a little upward on the ovaries; placentation parietal; capsule many-seeded. + +About 1,000 species: entirely tropical, especially from South America and East India. They are found chiefly among the underwood in damp, shady places; some, which are feathery (*Pepomisum*), live as epiphytes on trees; a few climb by + +**Curvemberia.** 365 + +roots—Umb. Several Piperaceae are used medicinally and for spices on ac- +count of their pungent properties and the essential oils found in nearly all parts of the plant. The following are official: "Black pepper" (this umbil, +dried fruit of P. nigrum Linn.) "Long pepper" (P. longum Linn.), "Cayenne pepper" +(climbing shrub, East India); "Cubeb" berries of P. cubeba (climbing shrub, Java). "Long-pepper" is the urpice inflorescence of P. longum, East India. + + +A photo of a plant with green leaves and small white flowers. + + +Fig. 360.—Piper longum (Long pepper). In addition to the bracts there are two struc- +tures resembling bracteoles. + +The leaves of *P. aurantifolia* (Maitake) are official. The leaves of the Betel- +pepper (P. betle) are also official, but they are used as chewing tobacco to form +the well-known East Indian intoxicating compound "Betel." A good many +others are also used. + +Other species of *Chiranthus* (Chiranthus, Hyoscyamus) have opposite leaves, +with stipules more or less united at the base, and inferior "drupes." Ophiola +pendulosa. Only endosperm. About 33 species, Tropical. + +**Family 7. Curvemberiae.** + +The plants in this family have a curved ovule, and most fre- +quently a bidentate seed (general) provided with fine, cuticular, +projecting warts, Fig. 361 D), with a curved, peripheral embryo en- +closed by a thin, membranous integument, Fig. 361 E), about 285 C, +365 F); for exceptions, see Fig. 360); the seeds in all cases are +borne on a centrally-placed, and in most cases free, placenta (they +are basal when the flower is only 1 ovule in the corolla; Fig. 364). +The flower is similar, hypanthium being absent (Fig. 361 B) (only +rarely epigynous) and usually 5-merous. The flower which is most +complete has 5 whorls (Ss, Ps), A5+5, G2+2–5), as in some +species of *Caryophyllaceae*, but in others it is reduced; in this +type it becomes reduced, the petals and stamens being suppressed, +so that finally 5 perianth-leaves, 5 stamens (opposite the perianth- +leaves), and 2 carpels (Fig. 361 F) only are present; for example, + + +A diagram showing the structure of a flower in the Curvemberiaceae family. + + +364 +DIOXYLEDONEX. + +in certain genera of the Caryophyllaceae, in the Chenopodiaceae, Amaranthaceae, and others. When the number of stamens is in- +creased to more than 5 in the whorl, it is always possible to show that some of the stamens have been divided. The number of the carpels and ovules is almost increased; in the highest there is a central placentation free from its own ovules, and in the lowest there are ovules; in those which are most reduced there is only a single ovule, which is placed centrally at the base of the ovary (Fig. 364). +Sometimes corollas are produced in the fruit, which is a many-seeded capsule in those which have one ovule, or a con- +ceded war where there is one ovule. In the most reduced forms the flowers are generally unisexual—Similar features are also pre- +sent in the vegetative parts. Almost all the species are herba- +ceous, the leaves being simple or compound, and often succulent. +The structure of the stem, especially in Chenopodium, Amaranthus, Nystag- +maceae and others, often differs from that of the ordinary Boleodendron. In the +woody parts of these plants there are often found several rings which resemble annual rings but which are formed by new cambium-rings arising out- +side the old ones which then cease to divide. + +Order I. Caryophyllaceae. Herbaceous plants, with round, +nose-like stem; leaves opposite, slightly amplexical, simple, with +seeds, undivided, entire lamina; stipules nearly always absent; the +inflorescence a cyme or panicle; petals usually 5; sepals 5; ovaries +cymes. The flowers are regular, or 6 or unisexual, hypogynous or +perigynous (5- or 4-merous with 2-3-4 carpels; calyx persistent; +corolla polytetramorous. The ovary is unilocular (or originally and +sometimes now) with 2-3-4 loculi (or sometimes with 1 loculus), with +free styles and 1-several curved ovaries on a central, free +placenta. The fruit is a nut or a capsule opening apically with long or short valves (text, Fig. 362); it may be double the carpellar. +For the key refer to the family. In some genera the ovary is simple. + +The flowers are usually perfect (text, Fig. 360). For $x$ see Amaranthaceae, +$y$ see $x$ (Fig. 360, 361 A) & $z$ (Fig. 361 B); for $w$ see Amaranthaceae. +$u$ see $x$ (Fig. 360, 361 A) & $z$ (Fig. 361 B); for $v$ see Amaranthaceae. +The carpels may be placed opposite to the sepals (Fig. 360) or opposite to the petals (Fig. 361 A, B). Without any other modification of the flower they may be placed between the sepals and petals (Fig. 361 C). The carpels are next found reduced to 2-3-4 (see the genus); their number may easily be recognized by that of the stamens. This is the construction in the majority of genera of this order; but in some genera it is modified especi- +ally. It may have (a) two flowers as described above, with $2+3$, (b) the corolla only open, or (c) both the petals closed ($A$–$F$, Fig. 361 C), or (d) all these as well as some of them open ($G$–$H$, Fig. 361 C). For example: *Sesuvia*, *Cerat- +tum*, and others, and finally, a series of genera form a curious complex. + +1 + +CURVATURES. 365 + +Tions of reduction which have become constant, and by a gradual series of steps, lead to the most reduced form, which has only 5 sepals and 5 (or even 7 or far as near as only 1) sepal-antennae (Fig. 363 D, E, F).—The rarest condition is that of the Silemataceae. The sepals-antennae are most frequently the longest, and bear notalities at the base (Fig. 363 A). In the more advanced forms, however, they are reduced in the lower portion (Fig. 360); these do not, however, reach to the top, and generally soon dis- +appear. The stamens are also reduced in number on the placenta in as many double rows as there are sepals-antennae. The stamens vary greatly in number from many to 1 to take place (Fig. 361). A com- +parison proves that the "free, centrally placed" plant is the primitive type, while the "single band ovule in Herminaria (Fig. 361), Selenum, and others, is also borne on the carpel. + +The vegetative branching is characteristic. One of the leaves in a pair is formed into a short petiole with a single leaflet; the stronger leaves stand in a 4-ribin, the fifth above the first one, and the branches are consequently arranged in the same manner. In the inflorescence, however, it is in a 2-ribin (Fig. 362), and this arrangement (Fig. 363) is most advanced. The bud of the first bracteole (a) becomes sometimes entirely suppressed, or in some this bracteole itself is suppressed. + + +A B C +D E F + + +Fig. 361.—F Diagrams of flowers of the Corynothylaceae: A Agrostemma; B Sibima; C Stellaria; D Ceripodia; E Parnassia; F Herminaria. + + +The most original type appears to be represented by the Alnusine. From this form on one side the Sileneae, adapted in a higher degree for insect-pollina- +tion, appear, while on the other hand the Ericaceae show various re- +ductions. + +I. ALNINE, SITCHTOCHYNE GROUP. Sepals free, and connected with them stellately expanded, slightly unguiculate (white or in- + +365 + +366 +**DICYCTYLEONIDEAE** + +*odorans* petals; those, however, often become suppressed (Fig. 365). The fruit is a capsule. +a. As many carpels as sepals (4 or 5). *Ceratium* (Chick-wood). The petals are bifid. Capsule cylindrical, frequently curved at the top, and opening by 10 teeth (Fig. 362).—*Relatichia* + +A, B, C - Section of a fruit, a fruit, a fruit, a section of seed. +Fig. 362.—*Ceratium* ovatum. A, fruit; B, cotyl; C, section of seed. + +differs only in the 5-toothed capsule with beld teeth.—*Spergula* (Spurry). The petals are not bifid, capsule 5-valved ; seeds winged. The leaves are linear, and appear as if placed in large numbers in a whorl, a branch being situated in the axil of each with leaves placed very close together. The flowers are white or yellowish. *Spergula* has 8n. Fn., As = n., or As, Gn., where n = 4 or 5. The corolla is often wanting. + +b. 3 (rarely 2) carpels (Fig. 361 C). *Stellaria* (Stitchwort) has deeply cleft petals. The number of stamens varies (see above). + +A, B, C - Diagrams of stamens and pistils. +Fig. 363.—*Ceratium* (E-concha) pedicelar : V (A) and d-flower (B, C). + +*Aceraria* has entire petals. (To this group belong *Alcea*, *Mothreugia*, *Holostelea*, etc.) The flowers are usually regular, but occasionally in the form of the seed and number of the capsule valves.) *Spergularia* has membranous stipules, as in *Spergula*.—*Holostelea.* + +2. *PANTHICHEAE* (Figs. 361 D, E, F; 364). Small, greenish + +CUNNEREDE. 367 + +plant. The leaves, in the majority, are opposite, with membranous +one stipule. The flowers are usually frequently arranged in small +clusters; they are small and insignificant, perigynous (Fig. 364) +or hypogynous. The corolla is in most cases wanting, and when +present is very small; in general the calyx-stamens are developed, +but the stamens are wanting (Fig. 365). The ovary is unilocular (Fig. +365). Ovary most frequently with 1 ovule. Fruit, if any, rarely a +capsule; it is enclosed by the strongly perigynous floral axis +(torus). + +*Corolla* (Knappell) is perigynous with boll-shaped torus; +no corolla; calyx-stamens are wanting or rudimentary; some +calyx-stamens may also be absent—*Corrigida* (Fig. 361 D); +*Illiciocarum*; *Paragymnia* (Fig. 361 E); *Herniaria* (Figs. 361 F, 364). + +3. *Silene*, Piek or *Carnation* Gaud. +The flowers are small, white, pinkish, red, and +gnatulose, white or red, petals, with out- +growths (ligula, corona, paracorolla) at the +throat of the corolla. These structures are +usually wanting; the corolla is often wanting; +they are merely outgrowths at the junction of +the limb and claw. The corolla, stamens +and ovary are frequently raised above the calyx; upon a lengthened peduncle (gyno- +phore), which has SS. PS. At 5-7; +fruits a capsule with many seeds. + +a. 5- (rarely 3-) carpelate ovary.— +Typical of the genus. The corolla is longer than the calyx; corona present. +The capsule is 1-5 or 6-celled, completely +1-chambered or 5-chambered at the base,—the genus has been divided accord- +ingly into two subgenera: *Melanosperma* +(Lychis), *Viscaria*. Some species are unusual by the abortion of stamens +or sepals (*L. repensita, diurna*). *Ageratum* (A. pilosum, Corn-cuckoo, Fig. +361 A) has a long-stalked calyx; the +corolla is wanting. + +b. Six-toothed capsule; +corona present in the majority.—*Corallus* has berry-like fruits which, +finally become dry berries. +c. Bienenblüte (2 styles, 4-toothed capsule)—*Dianthus* (Pink); +at the base of the calyx 1-several pairs of floral-leaves are situated; + +W. II + +308 + +DIGOTYLEDONAE. + +corona absent. The straight corolla is a peculiar exception—*Gypsotheca* has a campanulate, open calyx, -nerved, membranous between the nerves; corona absent; the flowers are generally small and numerous, in a large, paniculate dichasia—*Saponaria* (Soapwort) has corona. + +**Fam. 17. *Alchemilla*. Alchemilla has ordinary mericarps at the base of the chrys- +stomata (Fig. 362); they are frequently united by their bases, and the absence of cross-venation in the less conspicuous species) pollinate them- +selves. The flowers are usually white, but sometimes yellow (particularly firm and green). *Gynandromorphus* flowers are found in several species, and the c-flowers are thus generally more conspicuous than the Q-flowers. That this is the case with *Alchemilla*, is shown by the fact that the flowers of *A. alpina* (Fig. 363), which are very similar to those found in (Fig. 363), *Argyrella perpulchra* in dicoccosis (Fig. 365). The Silene is as a rule adapted for pollination by insects with long proboscis—especially butterflies, bees, and ants. In the *Silene* genus, the stamens are erect on the corolla-stem, later on the corolla-stem itself, then the stigma expand. The honey is secreted in a ring-like noecular round the base of the corolla or by corollas at its base. The flowers are often nocturnal, but also during the day or night in the evening (*Lycanthus* species), *Silene nutans*, *Saponaria officinalis*, etc., and like other night-flowers, are of a white or pale colour. +In some species of *Silene*, the flowers are white or pale pink; in others, however, they are yellow or orange; in some species, they are red or purple; in some, they are blue or violet; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, they are white or pale yellow; in some, +308 +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. +DIGOTYLEDONAE. + +**Curtensiaceae.** 369 + +majority are herbs, some are shrubs. The leaves are scented, or aromatic, but always simple and without stipules. The flowers are solitary, cymose, or +4-50 species; especially in the Tropics, principally S. Am. and E. Ind.; few are found outside these countries.—Only a few are used; some, chiefly F. serrata (F. serrata), F. odorata (F. odorata), F. pinnata (Picea +tail); Gymnophyllum globosum; Crudea citrata (Coel's-comb) remarkable for its fanciated inflorescence; *Allochrocea*. Some are employed as culinary plants, and some are used by a few of the E. Indian species the seeds are +farinaceous, and used for food. + +Order 3. **Chenopodiaceae.** Generally herbaceous plants like the +Caryophyllaceae, but the leaves are arranged spirally (except +*Salicaria*), and are simple, stipulate; they are generally feathery and sessile, or with short petioles; the flowers are small and numerous, whose large spherical terminal cell rarely falls away; otherwise they +are seldom hairy. The inflorescences are generally flower-clusters +borne in paniculi. Bracteoles generally absent. Flowers gene- +rally regular, bisexual, and perfect; sepals 3–5, usually 5; petals +are hypogynous; they are regular, small and inconspicuous, with single, +green, 5-leaved, but more or less united perianth; 5 stamens opposite +the perianth, and a 3–5-carpelled, unicellular ovary with 1 basal, +central style and stigma; fruit a small achene or nut-like body. Leaves +and stamens is reduced to 3–2–1–0. The fruit is generally a +seed—thus this flower and fruit are the same as in the reduced +Caryophyllaceae (Fig. 301 A). The seed is similar to that generally found in the family (for exceptions see the genus). + +The family is represented in the Tropics by about 700 spp., fig. 81E. There +is no indication of perianth or of corolla-stamens, which may be supposed to have belonged to the plant, but which are now entirely and completely suppressed. +Thus the flower is reduced to a single bud-like body (Fig. 301 B). The +perianth persists after the withering of the flower, and envelops the nut; it is very variable, and together with the position of the leaf, the form of the ovary, etc., gives rise to many genera. + +I. **Chenopodium,** Gossypium Gossypium (Fig. 365), has (or poly- +gamous) flowers, with regular 5-parted perianth (*O*); the em- +bryo is ring-like (*H*). The leaves have the ordinary flat forms. +—Chenopodium (Gossypium). The flower is hypogynous, and the fruit (which is compressed) perfectly free from *Muellera*, a collec- +tive fruit—fruit and seed being separate (Cuscuta Rhizom) by the perianth becoming finally flaky and coloured—*Beta* (Beet), +Manegold, Fig. 365) differs from all genera in the perianth, which +finally becomes cartilaginous, being epigynous (*D*). Small, most +frequently 2-flowered clusters without bracteoles, situated in a + +370 + +DICOTYLEDONES. + +long, interrupted axis (A, B); the flowers and fruits in each cluster are more or less united individually, and fall off together— + +A. - Stipa vulpina. +B. - Hellebore (H. nummularia). +C. - Salsola, Salsola grevei, has cylindrical or semi-cylindrical seeds. Perihith as in the preceding group ; the fruit is most frequently compressed. The two first mentioned genera differ from most of the others in the order in having a spirally-coiled, + +D. - Salsola oed. entryn. + +CERYNEDIE. +371 + +and not a ring-like embryo, so that the endosperm is slight or wanting. (Fig. 365). These plants are sometimes placed as a group by themselves, *Strychnos*—in contradistinction to which the others are termed *Cycloides*.—*Salviae* (Saltwort); leaves subulate, with spiny tips; the flowers have 2 spinous bracteoles; developing transversally to the back of the perianth.—*Cherophora* deviates from *Cherophora* chiefly in the embryo and want of endosperm. —*Eriogonum*, a genus of the *Salsola*, but a ring-like embryo; it differs from the others in being hairy. + +3. *Salidaceae, Glasswort Group.* *Salicornia* (Glasswort) has a very different appearance. The stems are succulent, jointed, and almost leafless; they bear at the nodes a pair of long, narrow and connate; there is a depression in the axil of each leaf, in which a small 3-flowered dichlamyde without bracteoles is sunk; the flowers have a trimerous perianth, 1–2 stamens and 1 carpel. No endosperm. + +4. *Atiripideae.* This group has most frequently unisexual flowers; the 3-flower has a 4–5 partiular perianth, but the 5-flower differs from it. *Atiripa* is monocious or polynormous, the 2- flowered form being the commonest; the perianth is short, which expands during the ripening of the fruit, and often become wasted and fringed, enveloping the compressed nut. The section *Dichotomosema* has two kinds of 5-flowers, one like those just described, the other similar to the *Oenothera* type. The former is found in S. *heterostyla*, in which the perianth is depressed, not pressed together from the sides; some (e.g., *S. heterostyla*) have even three kinds of flowers, while in *S. atiripa*, which is dioecious, there are two kinds of flowers: one with a long slender pedicel, numerous flower-duster, a rather singular arrangement—*Spinosia* (Salicion) in dichotomous; 5-flower: terminal, 4–5 stamens; 4–5 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; 5–6 stamens: filiform; 5–6 petals: tubular; + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +371 + +372 + +372 + +
+DOCUTYLEONIUS. +
+ +nibl; inhabiting salt-marches and salt-steppe, and growing as weeds (most frequently on gardens or field soil containing manure) in this country, especially species of Chrysanthemum and Arctia. The majority are found within the tropics, but some are found in the temperate zone, and others in the steppe. + +Umb. Comprising about 50 species, one is Ficus carolus (from the Mediterranean basin), with its different varieties, viz. Beek-wood, Cattail-wood, and Red-beet, Sugar-beet, and others. These are blooming, making in the first year a root of considerable size, and in the second year producing a stem of considerable length, and in the second year using this material in the production of a long stem, leaves and flowers. The primary root has been developed by cultivation into a very thick tap-root, which is the principal food-stuff of the plant. It differs from that of other roots, concentric rings of vascular bundles being formed from a cambial ring developed outside the previous ring. In this way several rings of vascular tissue are produced, each ring being separated from the next by a layer of parenchyma, may be found in the root of a Beet. Beteae Lactuca saligna, var. hortensis (Bettel-root), the following are also cultivated: var. celtica (Lesser-leaf), Mangold; var. sativa (Sow-cabbage); var. sativa (Cabbage); var. sativa (Spinach); a form of the latter and of Spinach are grown as ornamental plants. + +Order 3. Cucurbitaceae. The fruit is usually a berry or a berry-like fruit; the leaves are simple or compound; the flowers are perfect or imperfect; the sepals are 5; the petals 5; the stamens 5; the pistil 1; the ovary is superior or inferior; the fruit is fleshy or dry; the seeds are numerous or few; the fruit is either whole or united into a gynoeceum with a corresponding number of stamens in it. The following plants belong to this order: + +Order 3. Cucurbitaceae. The fruit is sometimes unicellular, regular, some times slightly perigynous flowers are inconspicuous and have a single sepallate or colourless 5-lobed perianth (usually united at the base); stamens either 5 or 4; petals 5; stamens 5; pistil 1; ovary superior; fruit fleshy; seeds numerous; fruit whole or united into a gynoeceum with a corresponding number of stamens in it. The following plants belong to this order: + +Order 3. Cucurbitaceae. The fruit is sometimes unicellular, regular, some times slightly perigynous flowers are inconspicuous and have a single sepallate or colourless 5-lobed perianth (usually united at the base); stamens either 5 or 4; petals 5; stamens 5; pistil 1; ovary superior; fruit fleshy; seeds numerous; fruit whole or united into a gynoeceum with a corresponding number of stamens in it. The following plants belong to this order: + +Order 3. Cucurbitaceae. The fruit is sometimes unicellular, regular, some times slightly perigynous flowers are inconspicuous and have a single sepallate or colourless 5-lobed perianth (usually united at the base); stamens either 5 or 4; petals 5; stamens 5; pistil 1; ovary superior; fruit fleshy; seeds numerous; fruit whole or united into a gynoeceum with a corresponding number of stamens in it. The following plants belong to this order: + +Order 3. Cucurbitaceae. The fruit is sometimes unicellular, regular, some times slightly perigynous flowers are inconspicuous and have a single sepallate or colourless 5-lobed perianth (usually united at the base); stamens either 5 or 4; petals 5; stamens 5; pistil 1; ovary superior; fruit fleshy; seeds numerous; fruit whole or united into a gynoeceum with a corresponding number of stamens in it. The following plants belong to this order: + +Order 3. Cucurbitaceae. The fruit is sometimes unicellular, regular, some times slightly perigynous flowers are inconspicuous and have a single sepallate or colourless 5-lobed perianth (usually united at the base); stamens either 5 or 4; petals 5; stamens 5; pistil 1; ovary superior; fruit fleshy; seeds numerous; fruit whole or united into a gynoeceum with a corresponding number of stamens in it. The following plants belong to this order: + +Order 3. Cucurbitaceae. The fruit is sometimes unicellular, regular, some times slightly perigynous flowers are inconspicuous and have a single sepallate or colourless 5-lobed perianth (usually united at the base); stamens either 5 or 4; petals 5; stamens 5; pistil 1; ovary superior; fruit fleshy; seeds numerous; fruit whole or united into a gynoeceum with a corresponding number of stamens in it. The following plants belong to this order: + +Order 3. Cucurbitaceae. The fruit is sometimes unicellular, regular, some times slightly perigynous flowers are inconspicuous and have a single sepallate or colourless 5-lobed perianth (usually united at the base); stamens either 5 or 4; petals 5; stamens 5; pistil 1; ovary superior; fruit fleshy; seeds numerous; fruit whole or united into a gynoeceum with a corresponding number of stamens in it. The following plants belong to this order: + +Order 3. Cucurbitaceae. The fruit is sometimes unicellular, regular, some times slightly perigynous flowers are inconspicuous and have a single sepallate or colourless 5-lobed perianth (usually united at the base); stamens either 5 or 4; petals 5; stamens 5; pistil 1; ovary superior; fruit fleshy; seeds numerous; fruit whole or united into a gynoeceum with a corresponding number of stamens in it. The following plants belong to this order: + +Order 3. Cucurbitaceae. The fruit is sometimes unicellular, regular, some times slightly perigynous flowers are inconspicuous and have a single sepallate or colourless 5-lobed perianth (usually united at the base); stamens either 5 or 4; petals 5; stamens 5; pistil 1; ovary superior; fruit fleshy; seeds numerous; fruit whole or united into a gynoeceum with a corresponding number of stamens in it. The following plants belong to this order: + +Order 3. Cucurbitaceae. The fruit is sometimes unicellular, regular, some times slightly perigynous flowers are inconspicuous and have a single sepallate or colourless 5-lobed perianth (usually united at the base); stamens either 5 or 4; petals 5; stamens 5; pistil 1; ovary superior; fruit fleshy; seeds numerous; fruit whole or united into a gynoeceum with a corresponding number of stamens in it. The following plants belong to this order: + +Order 3. Cucurbitaceae. The fruit is sometimes unicellular, regular, some times slightly perigynous flowers are inconspicuous and have a single sepallate or colourless 5-lobed perianth (usually united at the base); stamens either 5 or 4; petals 5; stamens + +CUNENSEX. 373 + +Order 6. *Portulacaceae* (Portulaca). The flowers are regular (except *Mentha*), hypogynous (except *Portulaca*) and 5. +The diagram which applies to the majority of genera is that in Fig. 367, but with all the 5 stamens completely developed: it may be considered as the Chloromodioscous diagram with the addition of a corolla, which is here represented by a tube con- +sidered as sepals, and with a petaloid perianth (namely design- +ated "corolla"). The "petals" fall off very quickly, and are sometimes wanting. Most frequently 5 stamens, situated oppo- +site each other on the same side of the flower, are found. *Mentha* +has only 3 stamens (by suppression of the two anterior and lateral, Fig. 367), others again have more than 5, some a large +and indefinite number. This may be explained partly by the asymmetry of the flower, and partly by the splitting (dedoublement) of the stamens. +Gynoeceum most frequently trimerocarpous, ovary unilocular with I—several basal ovules (sometimes on a +broad base), or with a single ovule (e.g., *Corydalis*, *Corydalis*, +*Phyllocladus*). The fruit is a capsule, more rarely a nut.—The majority are annual +herbaceous plants with scattered, entire leaves; often showy and fragrant, with +a perianth of 5 sepals (dry, mealy, +branched, modified into hairs). Inflorescence +cyme. + +*Portulaca* (Portulaca): flower, epigynous or semi-epigynous; +from a pyxidium. The stamens vary in number, and are most +frequently placed in groups (in consequence of splitting) opposite +the petals.—*Mentha*: the corolla is slightly gamopetalous, but +clefs on the posterior side (Fig. 367), and as a consequence of the +internal division of the perianth into two parts. S stamens. + +—Calandrinia: *Tallium*: *Amananthus*: *Claytonia*. + +125 species; mostly in warm and temperate countries, especially the arid parts of S. Am. and the Cape. *Mentha* *foetida* (Blass) is a native plant. *Portulaca* +olivacea is cultivated as a herbch in the south of Europe. A few species of +*Portulaca* and *Amananthus* are ornamental plants. + +Order 7. *Nyctaginaceae*. The characteristic feature of this +order is the single perianth-septate calyx, with a false petaloid; the +lower part of which generally persists after flowering and em- +braces the fruit as a false pericarp. The upper portion is most + +374 + +DIOTTLECOYENS. +frequently calcate and folioid, or simply valvate in estivation. +The number of stamens varies. The free gymnocarp is unicarpellate and has 1 ovule. The fruit is a mei, but becomes a false drupe, since the lower persistent portion of the perianth becomes dekay (as in Nee), where this feathery part is almost completely covered by the pericarp. In the majority of the Mirabilis the lower part becomes the dry anthocarp, while the upper petaloid part falls away after flowering. Finally, a peculiar type of fruit is formed by the flowers by free- united floral-leaves.—The majority are trees (Ficus, etc.), Bauhiniares is a liane. The stems are often nodose and swollen at the nodes; the leaves are simple, penni- +scent, scattered, or opposite, without stipules. In some, the vascular bundles are excurrent. + +Mirabilis; the structure of the stem is abnormal. Dichialous branching with continuation from the second bracteole, thus forming an involucre. The leaves are simple, alternate, oblong to lanceolate-shaped, and has a folded and twisted estivation resembling that of the corolla of the Convolvulaceae; the upper coloured portion falls off after the flowering. Outside, and alternating with it, is 5-6-parted, spiralous involucre of 5 spirally arranged leaf-like scales—Oryzaeptera. The flowers are in terminal dichasial flowers.—Bauhiniares: the involucre is rose-coloured, 3-leaved, and en- +velops 3 flowers (placed laterally); the terminal flower wanting. +The leaves of the involucre in Bauhiniares, Ficus, Nees, and others are reduced to tooth or scale. + +157 species; mainly in tropical countries, and especially R. Am. Species of *Strandia* (L.) Desr., with 2-3 stamens in each flower (the genus now disovered by Land in Laguna Santa Cruz), which may be used as a tea-plant. + +Order S. Alismaceae. Only 2 species are found in the flower, which alternate with one another when their leaves are equal in number. The first is sessile, the third pedunculate. In *Strandia* (L.) Desr., which is a monotypic genus, each is developed as a stamen, or it is divided into a large number of members which then all become stamens (arranged in groups), or the outermost ones become developed as petals (arranged in groups). The leaves are usually several-leaved. Most of the species are herbs with thick, fleshy stems, and exstipulate leaves. The structure of the stem is usually anomalous. + +A monotypic genus of aquatic plants with 2-3 stamens in each perianth- +leaves; stamens single, or (by splitting) in groups of 3-4, alternating with the perianth-leaves. The gymnocarp (with 3-5 carpels) has 5-8 loculi in the ovary, and some few cells between them. The pericarp is thin and consists of a fibrous format by the edges of the carpel. The fruit is a mei. The + +CAXTULFOE. +375 + +inflorescences are dichasium and unipared scapoid cymes—sinois, Mollugo, Sempervivum, and others—are herba or herbaceus, most frequently hairy. + +2. **Mecranthaceae** have semi- or wholly-epigynous flowers—*Tetra- +gonum*, *Lysimachia*, *Spergula*, *Spergularia*, *Stellaria*, etc.—or by +splitting in groups alternating with the perianth-leaves. There is an indefinite number of carpels, and each loculus of the ovary contains only 1 pendulous ovule; the style is long and slender, and the stigma is sessile; there is an accessory foliole below them; in some instances there is also an accessory flower between this bud and the flower. Southern hemisphere, especially at the equator, and in the tropics. The flowers are usually solitary, which is enlivened in a pot-bush (Japan, Austr., S. Am.). **Mecranthaceae**—Mecranthusus—the flowers are +numerous stamens all borne by the splitting of 5 or 4 protocarps (primordia) +alternating with the sepals. The ovary presents another characteristic peculiar to +this family, namely, that its loculi are not separated from one another (several +loculi) with the ovaries at first born, as in other cases, on the inner corner of the inwardly-turned sepals; but during the subsequent development the whole of the ovary becomes united into a single body, and the ovaries assume, apparently, a position very nearly met with in the vegetable kingdom: on the dorsal surface of the carpels. Shrubs or under-shrubs, more rarely trees. The flowers are usually solitary, but sometimes in pairs, which are +trilobular leaves, containing a quantity of water. The flowers open about noon, +and are highly odorous, generally red or violet, but olivaceous. The +ovaries are often sessile; they are found in *Cape* (South Africa), *Cape* +Grape. Some are ornamental plants. *M. cristallinus* (the ice-plant) and others are covered with peculiar, bell-like bristles; hanging hair; the out-slap of which con- +tains salt—these are used for washing. + +Family 8. **Cactiaceae**. + +The position of this family is very doubtful: but it seems in many respects to approach *Mecranthaceae*. Some botanists place it near to the Ribesales; others, again, to the Passiflorales. +Only 1 order. + +Order **Cactaceae** (*The Cacti*). The flower is epigynous, y, +regular, remarkable for its apocarpic structure: there are, for instance, a large number of spirally-septate sepals and petals, which gradually pass over into one another, and which in some species, to a certain extent, arise from the walls of the ovary as in *Nymphaeus* (Water-lily), *Oenothera* (Evening Primrose), *Oenothera* (Primrose), +*Opuntia*, *Pereskia*, and *Rhipsalis*—erect and united at their base into a shorter or longer tube in *Cereus*, *Epiphyllum*, *Mammillaria*, *Echinocactus*, *Melocactus* and others (Fig. 309). *Stenoma numerosa*, +although on the basis of its structure it might be placed in any family, +carpels with one style, dividing into a number of branches corres- +ponding to the number of carpels; the ovary has one loculus with + +376 +DECYOTYLEDONES. + +many parietal placenta; the ovaules are anatropous, on long and curved funiculi. Fruit a berry with cocciniferous seeds. The fruit-pulp is mainly derived from the funiculi.—The external + + +A: A section of a leaf. +B: A section of a flower. +C: A section of a fruit. +D: A section of a seed. + + +Fig. 365.—Eriocactus: a position of a leaf (A), a lateral slice on the digitated axillary bud, &c. (B). The fruit (C) is a berry with cocciniferous kernels which is separated by a foliole-leaf which has fallen off and left a scar (D). +The appearance of the Cactaceae is very peculiar; *Pereskia*, which has thick and bushy leaves (Fig. 368), does not belong to this family; the leaves of the *Opuntia* are usually small, and quickly fall off and disappear (*Opuntia*), or are modified into thorns; the stem, without normal foliage-leaves,—so characteristic a feature in this order,—is often developed cotyledons. The stems are fleshy, perennial, and may finally become woody; they are elongated, globose, pointed, and more or less dichotomously branched, e.g. in several species of *Echinocereus*. Some species, which live mostly as epiphytes on trees; in others, elongated, branched, globose, or more or less angular (prismatic) or grooved and provided with wings, and either solitary or in clusters as much as about 20 metres in height and 1 metre in cir— + + +Fig. 365.—Eriocactus. + + +POLYCARPICE. 377 + +carnifores; as in *C. giganteus* in New Mexico) or climbing by roots (Grewia and *Euphorbia* species); in others again, compressed, more or less leaf-like, often with a ridge in the centre (winged), branched and jointed; *Euphyllyum*, *Phyllodiscus*, *Omnia*, some species of *Iliogamia*; others are thicket, shrub, or tree-like, unbranched or only with a few branches; they either stand with prominent warts (mammites) each of which supports a tuft of thorns (Fig. 368 A ; Mammites and others) or with vertical ridges, separated by narrow rows (rows of mammites) of leaves (Fig. 368 B) in *Melochia*; *Eriophyllum* (Fig. 369); at the same time every one is embedded in the stem so that leaves or leaf-ears, with tufts of thorns in their axils, may be observed on the ovary just as on the stem—the flattened sheaths of the Cactaceae are formed in the same way; the flowers are usually in cylindrical axes (Omnia) or, as in *Melochia*, etc., from winged stems in which all the wings are suppressed except two. + +The thorns are produced directly from the growing points of the axillary bud, which is then transformed into a leaf-like structure with its sublinging leaf, which as a rule is extremely rudimentary; and these together form a kind of leaf-shrub, larger in some genera than in others. In *Eriophyllum* (Fig. 369), the leaves are very small, but in a large, conical sort (see Fig. 368 A), bearing on its apex the tuft of thorns and rudimentary lamina—such seedlings have normal cotyledons and a fully developed shoot. + +All the species (1000) are American (one epiphytic species of *Iliogamia* is found in Africa). *Mauritia* and *Caytonia* come from the tropical tablelands (Mexico); *Melochia* (Melochia) is found throughout America, as is *Iliogamia*, are epiphytes. *Omnia* varietis, the fruits of which are edible, is native to South America; *Euphyllyum* is found in South America and Asia; *Phyllodiscus* (Phyllodiscus) lives on thin and some closely allied species (O. costulatae, etc.), particularly in Mexico and the Canary Islands. Several are ornamental plants. + +Family 9. Polycarpice. + +The flowers as a rule are 5, regular and hypogynous; however in some orders they are unisexual, e.g. in the Myricaceae, or syconium-forms (in Monoknoides and Larkspur in the Ranunculaceae); in the Cactaceae they are usually solitary and sessile; and in Nymphaea (Fig. 368) even partially epiphytic flowers are typical. + +The flowers are acyclic in very many of the genera of the two first described families; but they are cyclic at any rate in the members of the second family, and corolla, thus dense or sparse. This type has a remarkable characteristic in that in the majority of the orders the number 3 pre-vails in the calyx and corolla; the number 5 also occurs, but the + +378 + +DICOTYLEDONES. + +number 3 is seldom met with. Most orders have a double perianth; chorisis does not occur, suppression is rare, and the parts of the flower are developed in acroptal succession. The most characteristic feature in the order is the free, one-lanced, as a rule numerous stamens (apocarpous gynostemium). The number of carpels in some of these orders varies widely down to one (e.g. Berberidaceae and Myricaceae). The carpels in Nympheaceae become united into one pistil (syncarpus), a condition which we also find distributed among other orders. + +Endocarp is usually absent all the orders (except e.g. Lamiaceae). + +The nutritive tissue in Cucubaleae and Nympheae is chiefly peri- +quem. + +Order 1. Ranunculaceæ. Nearly all are herbs (except Clematis); they have a large sheath with broad base (no stipules), and are most + +A diagram showing the structure of a Ranunculaceae flower. +Fig. 375.--Diagram of a Ranunculaceæ flower. +375 + +A diagram showing the structure of a Ranunculaceae flower. +Fig. 376.--Diagram of a Ranunculaceæ flower. +376 + +A diagram showing the structure of a Ranunculaceae flower. +Fig. 377.--Diagram of an Ranunculaceæ flower. +377 + +frequently palmarized with palmar lobes. The flowers are hypogynous, with most frequently a well pronounced convex re- +ceptacle (Figs. 374 B, 380), 5, regular (except Delphinium and Aconitum); their structure varies very much; in some the leaves are verticillate, in others arranged spirally; in others, both modes of arrangement are combined. In many cases it can be seen that the various series of leaves (especially calyx and corolla) are not so distinct or so sharply divided as is usual. The leaves of the perianth are often deciduous, but in some cases persistent, with more frequently extreme anthers ; gynostemium free, apocarpous (except Nigella and partly Heliotrope), with 1 or several ovules (Figs. 373, 378, 379) borne on the ventral suture. The fruitle is + +4 + +POLYCARPICE. +379 + +either a nut or a follicle (Actaea has bervio). The seed has a large, +oil-containing endosperm and a small embryo (Fig. 374). + +The main axis generally terminates in a flower, and the latter has a branch in its axil, which bears the leaves. There is no essential difference in construction : *verticillate* (recurrent), i.e. constructed all through of alternating whorls ; *angulata* (Fig. 375), *Xanthorrhoea*, and sometimes *Eriodictyon*. *Semi- +circularis* (Fig. 376) is a compound leaf, with two or more leaflets, and the others arranged spirally; *Renunculus* (Fig. 377), *Myosurus*, *Parnassia* and several other plants have leaves in two rows, one on each side of a central *recurved* (recurved) leaf, all the leaves are arranged spirally, so that several of the leaves do not alternate the one with the other, even though they are the same in number: in such cases the leaves are said to be *decussate* (decussated). *Caltha* (Fig. 378). The leaves of the calyx are in this instance arranged on a spiral of five; those of the corolla on 8, 9, 10, or 12, and stamens and carpels likewise on higher figures. + +The genera *Carduus*, *Acanthus*, *Tallacrisma* and *Clematis* have a simple perianth, which is most frequently petaloid; it is thus apparent that the sepals are petaloid in these plants also. In the genus *Carduus*, however, as in these instances stamens. The calyx is similarly petaloid in the genera *Heliotaurus*, *Erinacea*, *Nigella*, *Zephyranthes* and *Ranunculus*. As the petals are present in these instances, it follows that the sepals are also present in them, as well as the function of nectaries, a function they already possess in Ranunculus. According to this view, the sepals of the flowers of these plants are petaloid, although they have lost the function of reproduction; the perianth is then simple, and most frequently petaloid. Those leaves in the flowers of many Ranunculaceae which are arranged spirally are not always petaloid; but they are often those leaf-structures of the flower whose essential function lies in the production of nectar, and which, independent of the differentiation of the perianth into calyx and corolla, may be regarded as organs of reproduction. The structures of their circinate functions. Clear transitional forms are found between the two series of the perianth (c.g., between the sepaloid and petaloid perianths of *Leucanthemum* and *Lysimachia*) and between the perianth and stamens (as in *Helleborus*); but these transitions are never found between perianth and honey-leaves (with the exception of *Aquilegia vulgaris*, see infra). The leaves of these plants are therefore leaves which have lost their reproductive functions and agree with the stamens in their structure. In Ranun- +culaceae in their arrangement, development, and sexual system of veins (except in some species of *Ranunculus*), they agree with those leaves which form the front of the unpaired perianth-leaves are united into one, as shown by the veins (when three veins arranged symmetrically). The honey-leaves of *Aquilegia*, *Callit- +rhus*, etc., are similar to those leaves which form the front of their circinate leaves; but their circinate functions differ from those of their large circumference, as organs of attraction, and on this account are considered as petals by other authors. The same position in the flower which the honey-leaves occupy in these plants is occupied by them in some Cypripediums, in *Amanthus*, *Actaea* sect. *Eumecia* (e.g., *A. racemosum*, Clematis sect. **Aurea**), in some species of *Caltha*, etc.; but they differ from them in structure, in having three veins instead of two, etc., and in being deciduous. A perianth sharply differentiated into calyx and corolla, and deciduous or honey-leaves, is found in *Anemone* sect. *Eumecionia* (Cape), + +380 + +DECYOTYLOGONEX. + +*Adonis.* *Fernia.*—The perianth of the Ramnaceae is considered by Franzl to be usually petaloid.—The stamens arise in the Ramnaceae (1) on the normal anumum (Clematis sect. *Virenae*, 2) of the honeys-lower (this is generally the case with the genus *Adonis* and *Aristolochia*), but in the *Ramnus* (3) (see *Ramnus* species).—As the result of his researches upon the Ramnaceae, Franzl does not agree with the view advanced by Franzl (Schenk, *Hand. d. Bot*. iii.) that the perianth in general have proceeded from the antheromorph of the stamen (*A*). + + +A B C D + + +Fig. 571.—Diagram in longitudinal section : e the ventral anumum ; d the dorsal anumum ; +A, B, C, dorsal ; C, D, ventral. + + +The most primitive form of fruit is undoubtedly the pod formed by one carpel, on the edges of which (along the ventral anumum) two rows of ovules are situated: Funiculus, Helldorfera, Delphinium (Fig. 572). In a great many genera the number of ovules is equal to that of carpels, and they are arranged in a central plane under the lateral leaf-edges, and sometimes also some barren ovaless show it (Fig. 379). The fructification in this case become phyllodes, and are present in much larger numbers than when they are follicles. + + +A B C D + + +Fig. 572.—Helldorfera oedipus ; A flower ; B ramonanum ; C pod ; D seedling (seeds). + + +The following have FOLICULES: *Funiculus*, *Helldorfera* (except *Actaea*) and *Delphinium*; *Achenes*: *Ramunacium*, *Asimina* and *Clematidium*. + + +A B C D + + +Fig. 573.—Gynoecium : A flower ; B ramonanum ; C pod ; D seedling (seeds). + + +POLYCARPICK. +381 + +A. Follicles (Figs. 375, 379), with many ovoids, situated in two rows along the ventral surmise. *Actaea* has berries, *Nigella* has capsules of several benni. + +1. PANOISE, PENT GROUP. This has regular, septicil flowers with a narrow, most frequently 5-leaved, imbricate calyx; large, coloured petals, introrse anthers. + +Slightly perigynous. + +Surrounding the base of the flower is a ring-like swelling of the receptacle ("dorsum") is present, which is absent in *P. mentha*. The follicles are more or less dehiscent by a break in the leafy sheath. + +2. Hellebore, HELLEBORE GROUP. This has regular flowers with most frequently a coloured calyx; the sepals (separy- leaves) are modified into nectaries; they may be horn-like, provided with a spur, or of a different form; or they may be entirely ab- sent. Anthers often extrorse. + +---*Trollius* (Globe-flower). The flower is achyric: many + +According to Prenot, some species of this group, (e.g., *Aquilegia* and *Astrantia*) have a perianth, and others do not. *Aquilegia*, which does not pass over into the honey-leaves. The outer leaves at the perianth have freely opened instead of being immediately closed. + +Aquilegia vulgaris. +Fig. 376.—Aquilegia vulgaris. + +Caltha palustris (cat. 603). +Fig. 377.—Caltha palustris (cat. 603). + +382 +DIOTYLEDONER. +petaloid sepals, exceeding these, most frequently, several linear, +dark yellow petals, which bear a naked nectary at the base; +finally, many stamens and carpels arranged in a spiral (Fig. 375, 377); 5 (-7) yellow sepals, no petals, or 5-6 yellow petals with a greenish +Hellebore (Hellebores) has pedate leaves. The flower is axillary, +with a large, regular, persistent, often petaloid sepals (1) ; small, +korulbe petals (honey-leaves; most frequently 13, divergence 4%) and greenish sepals (Fig. 374). -Aegopodium +Erabtis (Water Aconite), like Hellebores, has 3-leafed involucre and most frequently trimerous flowers. 6 large petaloid sepals, 6 petals (lobular honey-leaves), 6 oblique rows of stamens, 8-4 carpels. +Aquilegia (Columbine, Fig. 370); the flower is entirely cyclic + +Fig. 379.—Nigella. A B fruit of N. annuaea, entire, and cut transversely. C floral +(only one flower shown). + +and has large apers on all the petals (funnel-shaped honey-leaves); S5 coloured, P5 A5 (8-12), G5 in regular alternation +(Figs. 370, 371); the innermost stamens are often stamindoes +(Fig. 370)—Nigella (Love-in-the-mist, Fig. 375) has 5 sepals +and 8 modified stamens; the outermost stamens are covered by the under-lip; Fig. 378 C, D). The 5 carpels are more or less completely united; and a many-carpellate ovary with free styles is formed in some. Large air-chambers in the external part of the sepals (Fig. 378 E); Fig. 379—Artemis (Blueberry) has coloured sepals, either no petals or an +sometimes present transitional forms to the innermost, and sometimes there is a distinct boundary between them. + +A diagram showing the structure of a flower with five sepals and five petals. +B Diagram showing the arrangement of stamens and carpels in a spiral pattern. +C Diagram showing the innermost stamens being modified into stamindoes. +D Diagram showing the outermost stamens being covered by the under-lip. +E Diagram showing large air-chambers in the external part of the sepals. + +POLYCARPICE. 3-3 + +indefinite number, and only 1 carpel. The fruit is a berry (or foliole) —Cuniculum, Geridula, Xenanthus (85, FS, p. 45-45). +3. Dicarpellate. The fruit is a berry. Zygomorphic flowers with coloured calyx; the 2 interior petals (flamboyant-leaves) are transformed into nectaries, the others are small or absent altogether. +—Annonum (Monkshood). 5 sepals, of which the posterior one (Fig. 372) is usually the most frequently 8-petalled (as in Fig. 372), of these the two posteriors are often large and long, and the two anterior ones are small and short; the latter are sometimes suppressed. +—Delphinium (Larkspur). Very closely allied to Aconitum, but the anterior 4 petals are most frequently wanting, and the 2 posterior ones have each a spur, which is enclosed by the posterior petal (Fig. 373). +—Dichondra (Dichondra). Flowers provided with a membranous spur. Sinema and carpos are radially placed; the petals 5, 6, 7, 8. +In \( \omega \), epigynous and conical; in \( \Omega \), apparently only 1 petal (by the fusion of the stamens); the fruit a berry. + +B. Fruit achene. Many carpels, each with only 1 ascending (Fig. 373 C), or pendulous (Fig. 373 D) and bearing a single rudimentary ovule above it (Fig. 373 A, B). + +4. Racemose. Bracteate. The fruit is an achene; the achene has double perianth. +Myosurus and Aesculus have pendulous ovaries as in Annona. +—Aesculus (Hickory). Aesculus hippocastanum and Ficuscar, orectocarum (Fig. 215 G) and downwardly-placed radicles —Rhamnaceae. +Many spirally-placed stamens and carpels (Figs. 371, 380). The petals (flamboyant-leaves) have no nectaries; the calyx is small and variably wrinkled; dimorphic leaves. Ficuscar has 9 sepals and 7–8 petals arranged in \( \omega \) – F. macrophylla (the latter usually having only one petal); the fruit is hanging from the peduncle; the flower is very similar to that with which, these are organs of reproduction. +The embryo has only 1 cotyledon —Myosorus (Monsun-tail) has W. B. + +A small diagram showing parts of a flower. +A B C D + +384 + +DIGITOLOXON. + +small prolongations from the 5 sepals; 5 narrow petals which bear +the nectaries near the apex; sometimes only 3 stamens, and an +ultimately very long receptacle, with numerous spirally- +arranged achene (Fig. 381).— + +Achenes usually solitary (Fig. 379), most frequently 5 sepals with +5 indefinite stamens and car- +pets of 1 or 2. The corolla +has 5 lobes. + +Fig. 381.—Flower of *Ranunculus sceleratus* Linn. + +5. ALEXANDRA, *Alexandra*.— +GROCH has a single perianth. +(*Pandanus odoratus* Fig. 378 E), radicle leaves, the flower has a +single, petaled, most frequently 5-6-lobed perianth, and beneath +the flower most frequently an involucre of 3 leaves, placed close +together in the form of a whorl. In *A. nemorosus*, *ranunculoides*, +etc., the involucral leaves resemble foliage-leaves; in *A. hopstatic + +A diagram showing the structure of a plant's flower. + +Fig. 381.—Mysorensis minorum: e nodiflorum; m the foliage-leaves; f the floral axis +with its perianth; g the involucre with its leaves; h the flowers; i the stamens; +they are situated close under the perianth, and resemble sepals, and in the sub-genus *Palastilla* they stand between the foliage- +leaves and floral-leaves. The style of *Palastilla* finally grows out + +POLYCYLACEAE. +385 + +in the form of a feather. The main axis of A. leptocis has unlimited growth (it is bisexual), and the flowers are borne laterally in the axils of the seashaves; and the flowers in the chena (uniaxial) the flower is terminal, and the rhizome is symmetrical after flowering. The genus *A. leucostachys* (Meadow Rau) has involucre with 4–6-leaved, greenish perianth, and the re- +ceptacle is flat. The stamens are bright-yellow-coloured and have long filaments; 1-6 accessory flowers may occur in the leaf-axils of the panicle-like inflorescences. + +6. CLEMATIDEAE, CLEMATE GROUP. This differs from all the others in the volute notations of the calyx an f its opposite leaves. There are 3–(several) petaloid sepals ; petals are absent, or limited to one or two, or none at all. The leaves are simple, with prolonged, feathery style. The majority of the genera are shrubs, and climb by their sensitive, twining leaf-stalks — Clematis — Clematis. +Atrogene. + +Foliation. The flowers are conspicuous either by coloured pedals (Clematis, Clematideae, Pecosia) or coloured sepals (Helichrysum, Artemisia, Galium, etc.), or by both (Aquilegia, Delphinium), or by the coloured stamens (Thalic- +trum). Some have no hairy calyx (Clematis, Anemone, Thalictrum), and are gener- +ally glabrous; others have a hairy calyx (Anemone, Oxyria), or a hairy corolla (Gentiana, Trollius, Heliotrope, Nigella, Aconitum), and are gener- +ally hairy on the sepals (Pulsatilla), or on the petals (Caltha), or on both (as for Narcissus). The flowers are usually sessile on the stem; but in some species they are sessile on the petiole (as for Narcissus); or on a short stalk (as for Aquilegia, Delphinium, and Actaea). Helichrysum and some *Brunnera* +species are protogynous. + +A few genera are cosmopolitan in northern temperate climates, and extending to the Polar and Alpine regions. Only the Clemates are tropical. + +The order has an abundance of aerial, vascular plants (Asclepias, Acaulis, +etc.) with large leaves; and of aquatic plants (Hydrocharis morsus-ranae). +Acetum napellus (perennial leaves and tuberous roots); the rhizome of +Hydrocharis caudata from N. Am. (the alkaloid hydrastine); the onion, hori- +zonium; and other plants which yield medicinal substances; many have +species which are cultivated for their beauty. Sweet-scented flowers are abundant. + +Order 2. NYMPHAEACEAE. Water Lilies. Water Plants ; +generally with large, floating leaves; and large solitary flowers ; +sepals 3–5; petals 3–5; stamens 6–20; carpels 8–20. The flower is hypogynous, but in the Nympheae different degrees of epigyny are found, and from this fact, as well as from the carpels being reduced into one pistil), it is clear that these plants differ from +the Ranunculaceae with much greater modification. The seed often has an aril; and, in the majority, a farinaceous nutritive + +386 +386 +**EUCOTYLEDONS.** + +these, partly endosperm, partly perisperm (Fig. 383 C). The embryo has 2 thick cotyledons and a small hypocotyl; the plasmalem is well developed, with 2-4 leaves. + +1. **Cannabium.** 3-4 species (Tropical S. Am.), resembling the Water Baumeanus, with two kinds of leaves, the submerged being dissected and the aerial pinnate. The leaves are simple, entire, and alternate on the submerged carpellus. The ovules are situated at the central line of the carpel--an unusual unique circumstance. Endosperm and perisperm. Colombia; Venezuela. + +2. **Nelumboeae.** The leaves are petiolate, raised on long stalks high above the water. Large, hypogynous flowers (Fig. 382); sepals 4-5; petals 4-5; stamens numerous; ovary 1-celled, sessile, subterranean; the receptacle is very remarkable, being raised above the stamens, and developed into an inverted conical body on the apex of which the nutlets are enclosed in pits. Fruits are enclosed in pits. The seeds are large and have well developed cotyledons. + +3. **Nympheaeae.** Water Lily Group. The carpellus is united into one, monochlamydean ovary, with a single ovule situated on the surface of the partition wall (as in the Poppy); and radiating, the number of rays corresponding to the number of carpellus (Fig. 383). The fruit is a capsule with many seeds, which have a large pericarp in addition to the endosperm (Fig. 383 C). + +Sepals, petals and stamens often pass gradually over the one into the other, the petals becoming narrower by degrees, and bearing anthers on each side of the apex, which gradually become larger anthers in proportion to the filament, until the perfect stamens is reached (Fig. 383 D). The long-stalked leaves are floating, and most frequently cordate, elliptic, lanceolate, with a shiny surface, sometimes (as in Victoria regia and Euphrasia) with strongly + +Fig. 383. Nelumboea nucifera; vertical section. +*Innominate flower of Nelumbo nucifera.* + +POLYCYLIPICE. 387 + +projecting thorny ribs on the lower surface. In the intercellular passages of the leaves are some peculiar, stellate cells. + +Nepher has 5 sepals, and an **angiosperm** flower. The petals, which are small, have a nectary on the back; the coloured inner side of the sepals forms a nectary, and the outer side is white. The flower is a native plant (Yellow Water-Lily), with, most frequently, 18 petals and 10-16 leaflets in the upper part of the stem. The flowers are sessile, and bear on its under surface a number of roots, which on drying-off leave deep scars; the leaves are borne in spiral lines, and the flowers are solitary in certain unfaults. The circumference of the stem is irregular; the vascular bundles are scattered and closed in as a monocotyledonous stem. + + +A: A flower in longitudinal section, the most external leaves having been removed. +B: A seed of Nepher (longitudinal section); the pericarp at the base, +C: A seed of Nepher (transverse section). + + +Nympheus has 4 sepals, and the flower is more or less epigynous. Petals and stamens are inserted at different heights on the ovary to just beneath the stigma (Fig. 3SS). Nympheus alba (White Water-Lily). *Victoria regia* from the Amazon, and *Euryale ferox* from South America, are large water-lilies. The leaves of *Victoria* are as much as 2 metres in diameter, and the edge is bent up to a height of 5-4 cm.; the flowers are 20-30 cm. in diameter, and change in colour from green to yellow; they open at night, close during the day, and at 14°C. above the temperature of the air, together with a strong formation of carbonic acid, has been observed during flowering. + +Nepher has 5 sepals, and is a native plant of the sub-genus *Symphytopea* are self-pollinated; the sub-genus *Lipocleptes* is insect-pollinated. Nepher is a native plant of South America; it grows in swamps, often in entirely closed and submerged flowers.—The dissemination of the seeds in *Nepher luteum* is effected by the fruit, which rests on the water, becoming de- + +3SS +DODTYLEDONEX. + +tained from its stalk, and deburring from the base upwards so that the seeds are net free, while in Nympheas only the spirally-twined stalk draws the fruit under water, and its deburring by its upper part being drawn off as a hood, and the seeds which are attached to the lower part of the stalk, and are thus carried away. In this condition they are able to float and can only sink to the bottom when the air has disappeared. + +38 species of fresh water in all parts of the world, but especially in the Tropics. The thorns and seeds of some may be used as food: *Euglypha ferrus* is even cultivated. *Nympheas cordata* and *Lazarus* were named among the Egyptians. + +Order 3. Ceratophyllaceae. About 3 species. Aquatic plants, submerged, rootless; leaves cartilaginous, verticillate, dissected into repeatedly dichotomous branches which are finely articulated; only one of the leaves in a shoot supports a vegetative branch. The flowers are regular, hypogynous, and with 6 perianth-leaves; stamens in the $q^{\text{5}}$ flower 10-20 stamens with thick connective, and in the $q^{\text{4}}$ flower a gynoecium formed by one carpel, with one orthotropic and pendulous ovule, which has only one placenta; style long, slender, and straight or curved on each side at pointed horn, and at the apex a similar one, formed by the persistent style. The embryo has an unusually well developed plumule with several whorls of leaves. The plant is rooted throughout its whole life—Ceratophyllum (Horn-wort). + +Order 4. A. **Amaranthaceae**. 3 genera; 7 species; 1 genus (united); succulent (as in the Rosaceae) or narrow linear segments and an episcopic gymnosperm; the flowers are irregular, regular and $q$, generally very large; petals usually 5 or 6; sepals 5 or 6; stamens numerous; filaments short or long; anthers oblong or oblong-lanceolate. The majority have synerpse with berry-like fruits, but in *Aeonium* and *Mannia* some of these species have become into a large, leaf-like fruit—a leaf-like fruit is also found in *Sedum*. The flowers are in *Mnogolacis*—Trees or shrubs with alternate, simple, entire, penninerved leaves without stipules. 450 (700) species; especially tropical. The best known are *Amaranthus*, *Chenopodium*, *Gypsophila*, *Lobelia*, *Lysimachia*, *Nemophila*, on account of their large, delicious fruits. Some have aerial and aximal prophylls (Zyloploca). *Gypsophila*—The flowers of the latter yield Ylang-ylang! Anthocyanin. + +Order 5. Magnoliaceae. Trees or shrubs with scabrous, often leathery, entire leaves, sometimes pinnate; flowers regular or irregular; sepals 5 or 6; petals 5 or 6; stamens numerous; anthers oblong or oblong-lanceolate and form a bud; the podarne internodes above them, and are cut off by the unfolding of the leaf next, leaving a ring-like scar. The embolomer is not removed. + +**A. MAUROVORUS**. The flowers are borne singly, and before opening are en- volved in an orbicular spathe which corresponds to the stipules of the foliaceous leaves. The petaloid generally consists of 4 or 6 recurved whorls, the external one of which is sometimes equal (Liriodendron), and the majority of Magnoli- + +POLYCAENIAE. +389 + +species), sometimes colored like the obovate; the perianth is sometimes many- +lobate. Numerous spirally placed stamens and carpels. The latter are situated on the elevated, cylindrical receptacle, and are individually more or less unisexual, but in some species (e.g., *Polycaenia* *oblonga*) the stamens and carpels alternate. The fruitulis in *Mauritia* open along the dorsal and ventral sutures, and the seeds then hang out, suspended by elastic threads formed from the vascular bundles of the perianth. The seeds are covered with a thin, fleshy, external layer of the shell being flesh-like—very rare occurrence. + +*E. ilicier* has no stipules. The carpels are situated in a whorl on a short receptacle, which is often prolonged into a long, tubular calyx containing essential oil. *Tiliaceae*, *Zoysia*. + +To the order of dicotyledonous dicotyledons: some in Europe or Africa. They are chiefly used as ornamental plants, e.g., the Tulip-tree (*Liriodendron tulipifera*, N. Am.), Magnolia grandiflora (N. Am.), M. ×yatei and *Forsythia* (China). + +Order 7. Magnoliaceae. The magnolias are large trees with pinnate leaves, axillary racemes, and persistent sepals. The flowers are bisexual and Tertiary types—the fruits of *Ilicium* extant (Sinan-animal from Eastern Asia) are opisthocarpous. The bark of *Drimys winteri* (S. Am.) is also stimulant. + +Order 6. Calycanthaceae. These are very closely related to the Magnoliaceae, +but differ in having perigynous flowers with many perianth-leaves, stamens +behind them, and a single ovary with one or two locules. The leaves are pinnate +with rolled up, leaf-like cotyledons, and leaves opposite on a square stem.—There +are some species in N. America (*Calycanthus floridus*, *Calycanthus occidentalis*, etc.) and +in S. America (*Calycanthus sp.*). + +Order 7. Monimiaceae. Aromatic shrubs with opposite leaves. Perigynous +flowers with many perianth-leaves, stamens behind them, and a single ovary, +and the Monimiaceae may thus be considered as an apocarpous form of this order. +They are also closely related to Calycanthaceae. + +**Order S. Berberidaceae (Barberies).**—The regular, $\gamma$, hypogynous flowers are dimorphic or trimerous and have regularly alternating whorled of free sepals, petals, and stamens and + +Fig. 304.—Diagram of Berberis. +Fig. 305.—Berberis carpel with 3 stamens. + +1 unilocular carpel; the corolla and stamens have each 2 whorls, +the calyx at least 2. The anthers open, as in Lauraceae, by +(2) ruffles, but are always introse (Fig. 304). The pistil has + +350 + +DIOSCYLIDOPHYCEAE. + +a large, fine-like, almost sessile stigma (Fig. 385), and in the ovary several erect cyliners are placed close to the base of the central suture. The fruit is most frequently a berry. Seeds endospermous. --Shrubs or herbs with scattered, most frequently compound leaves (without stipules), and racemose inflorescences.--They show a relatively great diversity in the form of the fruits and of the deliciosities of the anthors. + +*Berberis* is a shrub; it has sepals 3+3, petals 3+3, stamens 3+3 (Fig. 384). The petals (honey-leaves) bear internally at the base 2 darkly colored scales, which are conspicuous at the base, and suddenly bend backwards if touched at that spot (Fig. 385). The rammer often have a terminal, 5-merous flower; they are borne on dwarf-arbusculae. The leaves on the long-branched develop into thorns, but on the short-branched they are reduced to simple leaves. The short-branched with simple foliose-leaves, aristulated at the base, from which fast some leaves fall off. *Berberis* has important medicinal properties. A flower has 3 whorls of sepals. Otherwise as in *Berberis*--*Berberidaceae*: *Berberis*, with spurred petals; the flowers dimorphic; 4-5 whole of sepals; 5-6 petals; 5-7 stamens; 1 pistil. --The authors of *Phytogynum* deduce longitudinally.--*Nandina*. *Acanthus*. 100 species; North temperate, especially Asia; found in Euriptera. *Berberis* vegetates in a wide range of habitats; it is a plant with a long life span. *Aquilegia* (N. Am.). *Euphorbia* alpinae, etc., are cultivated as ornamental plants. Several have a paler colouring matter in the root and stem. *Oxypogon* (N. Am.). *Corydalis*. *Polemonium*. *Ruellia*. *Platycladus*. Order 10. *Manzimpergum*. This order has derived its name from the more or lessensonable fruits and seeds. Dioscius. The flowers are 3-6 merous, most frequently as in *Berberis* (*S.* 3+3, A.* 3+3, B.* 3+3), with the difference that the number of petals is not always equal to the number of stamens; however, the number is different. Stamens often united into a bundle (as in *Gymnocalycium*) or anthors debuding longitudinally; fruit a drupe. The plants (with lanterne-like flowers) are mostly climbing plants, and have scabrous, palme or palmette, sometimes leafed leaves without stipules. Structure of stem anomalous. *Cucurbita*, *Mesembriopsis*, *Cucurbitaceae*. 100 species; Tropical: very much better and poisonous properties. Oxyris. Chlorophyllous herbaceous plants with long-lived roots; they are cultivated as ornamental plants--*Mesembriopsis campanuloides* (N. Am.) and *E. debilior* (Asia). The fruits of *Jasminum cordatum* (N. Am.) are very poisonous--*Gratiola*. Order 11. *Lindahalacanthus*. This order, by the free, apocarpsic leaves, belongs to a more primitive type, and by the united stamens to a more developed one.--*Adenocarpus*: probably climbing or twining shrubs. About 7 species in S.E. Asia and N.Am. + +1 + +POLYCARPICEAE. +391 + +Order 11. Lauraceae (True Laurels). Trees or shrubs; the leaves, always without stipules, are simple, most frequently serrated, lanceolate or elliptical, entire, pinnate-lobed, finely reticulate (except *Cinchona* with 3-veined leaf), leathery and evergreen (except, e.g., *Laurus nobilis*); they are frequently studded with glands. The flowers are axillary, solitary or in panicles and are small and of a greenish or whitish colour. They are regular, perigynous, with most frequently a bowl or cup-shaped receptacle (Fig. 385), usually 2-, 3-, and trimerous (nearly dimorphic) though rarely 4-parted (e.g., *Laurus nobilis*). The calyx is generally perianth of two whorls, stamens 3-6 and carpels 1 (*Pistacia*, *Aesculus* +3 +3, 63) in regular alternation (Fig. 387). Each of the 2 or 4 bract of the anthers open by an upwardly directed sulcus (Fig. 386); of the stamens, the 2 outermost whorls are generally introsecant. + +Fig. 386.—Cover of the inner involucre of *Pistacia terebinthus*. (Sectional section). +Fig. 387.—Typical dissection of *Pistacia terebinthus*. (Sectional section). +Fig. 388.—Leaves of *Laurus nobilis*. (Sectional section). + +The calyx is persistent and surrounds the receptacle (Fig. 385). + +The ovaries are subglobose to ovoid, sessile or subsessile, 1 locular with 1 style and 1 or 2 carpels (Fig. 386), and may be considered as formed of 3 carpels. The fruit is a berry (Fig. 388) or drupe, which often is surrounded at its base by the persistent receptacle (as in *acorn* by its cupule), which becomes fleshy and sometimes coloured during the ripening of the fruit. + +The Lauraceae present affinities with the Polysspermae, in which they is found polygynous, as well as a similar number of parts in the flower and a similar gynophore. In this respect they differ from the Polypogonaceae; but their characters they should be classed among the Polypogonaceae, but stand, however, isolated. + +392 + +DICOTYLEDONER. + +by the episcopous gynoecum, if it is in reality formed by 8 carpels and not by 1 only. +*Herrania*, which has epigynous monoeccious flowers, deviates most. +*Corymbia* is a Concrate-like, herbaceous, slightly green parasite with twining, almost leafless branches. The leaves are reduced to a few narrow leaflets. Some Lauraceae have curved veins or palmented or lobed leaves (often together only on one side). + +There are 1000 species; especially in the forests of tropical S. America and Asia, of which they form the principal part. Only *Laurus nobilis* is found in Europe, and there is little doubt that its proper home is in Western Asia. + +Fig. 368.—Myrciaria: fruit. +Fig. 368.—Seed with well-erect and in longitudinal section. + +They are rare in Africa.—On account of the extensive oil found in all parts of the plant, they are used as opium, e.g., the false Cinchona (Cinchona officinalis), the coffee-tree (Coffea arabica), the coffee-bush (Coffea canephora), the coffee-plant (Coffea arabica), the coffee-bush (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica), the coffee-plant (Coffea arabica). The Lauri- +tree (*Laurus nobilis*, Mediteraneanan); her berries and leaves of which give +leather oil; also *Laurus carnea*, a tree of S. America; *Sassafras officinale* from N. Am.). The wood from its roots is official. +Fischerin "laurus" are large corydolous of *Nucifera pichuy*, whilst th + +KHOAINE.E. + +393 + +famous "Grasshout" wood of Damarana is the wood of *Nectandra radiata*. The pulp and seeds contain a fatty oil. The pear-like fruits of *Persea gratissima* (Mexican, also cultivated) is very delicious. *Lindera benzoin* is a valuable aromatic tree of India. + +Order 12. Myricaceae (Nutmegs). In this order there is only 1 genus, *Myristica*. Trees or shrubs. The leaves agree closely with those of the family, but the flowers are much more beautiful. The majority of the species are aromatic, having in their vegetative parts palisoid cells with abundant starch granules. The seeds are usually covered by a hard shell, and the fruit is often a drupe. The most important species are *Myristica fragrans* (nutmeg), *M. officinalis* (myrrh), and *M. carrii* (clove). + +In the 5-flowered the anthers vary in number (3–15), and they are exterior to the petals. In the 4-flowered the anthers are usually united into a column, unilocular, unicellular, with 1 scale. The pericarp (Fig. 389) has the form of a pear: it is a flabby, yellow capsule, which opens along the ventral and lateral sutures. The seed is enclosed in a hard shell, which is internally branched trilobed—the so-called "mace"; the "mantle," on the other hand, is the seed itself with its inner portion of the testa, which has pushed in by rupture of the outer portion of the testa. The seed is edible, but not yet used (Fig. 390); the external, dark brown, hard, and brittle part of the seed-shell is however removed. Made and eaten contain volatile and fatty oils in their proportionate quantities. The oil is used in perfumery and medicine for their aromatic seeds and oil, the most important being *M. fragrans* (nutmeg), from which nutmeg oil is obtained; *M. officinalis* (myrrh), from which myrrh oil is obtained; and *M. carrii* (clove), from which clove oil is obtained. + +The seeds of many species are used medicinally in Europe in every ancient time (e.g., by the Romans), but it was not until the year 1500 that the tree itself was known. The seed is nutritious. + +Family 10. Rhoeadeae. + +The plants belonging to this family are almost exclusively her- +bacious, with scattered, exstipulate leaves. The flowers are eucalyptal +or campanulate; the sepals are free or united at their bases; the petals +are regular; thynocarpus with 2—several carpels (generally 2, trans- +verse placed) (Figs. 391, 392, 393, 397). The ovary is unilocular +with parietal placentae, but in *Craesneria* and a few others it becomes +bilateral; the style is short or long; the stigmas are numerous or few across +the placenta. The stigmas in the majority of cases are connate- +ural, i.e., they stand above the placenta; and not above the dorsal +line of the carpels. The fruit is rarely always a cupule, which +opens by one or two apertures; but in some cases it is a dry indehiscent +valves, bearing no seed, whilst the placenta persist as +the seed-bearing frame. +Endosperm is found in *Pauarscorus* and *Pauarrocus*, but it is absent in *Craesneria* and *Crapadonardus*. This +family belongs to the order of the Magnoliaceae (the Symmophyta), +through the Cupressaceae to the Rhoeadeae in the next family. + +Exceptions to the above are: Echachlochus, Sabularia (Fig. 403) and a few + +394 +DIOTYLLIOEAE. + +Cupuláriaceae, in which poriogenous flowers are found. A few Papaveraceae and Fumariaceae have trimerous flowers. In Fumariae and certain Cruciferae, the fruit is a nut. The Papaveraceae are mostly 5-carpellate. Trees and shrubs are almost entirely confined to the Cupulariaceae, in which no species also are found. + +Order 1. Papaveraceæ (Poppies). Herbaceous plants with trifoliate leaves (Fig. 391) with 3-lobed leaflets, 2-3(-5) sepals (which fall off as the flower opens), 2+3 petals (imbriicate and crumpled in the bud) without spur, numerous stamens in several alternating whorls (generally a multiple of 2); carpels 2- several, united into a unilocular gynoecium. Trimerous flowers also occur, but the sepals are free, the petals connate, the ovary placentate; embryo large, with large, ovoidous endocarp (Fig. 392); the leaves have no stipules and are generally pinnately lobed. + +A diagram showing the structure of a flower of Glaucium and its dichotomous (which becomes monopodial) stem. +Fig. 391.—A diagram of the flower of Glaucium and its dichotomous (which becomes monopodial) stem. +end B + +B diagram showing the structure of a flower of Papaver argemone, illustrating the position of the stigma. +Fig. 392.—Papaver argemone; a gynoecium; e sepals; v valvula; b corolla; c stamens; d pistil; f anther; g anther filaments; h anther connective; i anther locule; j anther cavity; k anther lobe; l anther lobe apex; m anther lobe base; n anther lobe middle; o anther lobe side; p anther lobe tip; q anther lobe base; r anther lobe middle; s anther lobe side; t anther lobe tip; u anther lobe base; v anther lobe middle; w anther lobe side; x anther lobe tip; y anther lobe base; z anther lobe middle; aa anther lobe side; bb anther lobe tip; cc anther lobe base; dd anther lobe middle; ee anther lobe side; ff anther lobe tip; gg anther lobe base; hh anther lobe middle; ii anther lobe side; jj anther lobe tip; kk anther lobe base; ll anther lobe middle; mm anther lobe side; nn anther lobe tip; oo anther lobe base; pp anther lobe middle; qq anther lobe side; rr anther lobe tip; ss anther lobe base; tt anther lobe middle; uu anther lobe side; vv anther lobe tip. + +Papaver argemone: a gynoecium; e valvulae; v valvulae apexes of the stigmae; e valvulae valves of the stigmae; b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvulae valves of the stigmae, b corolla petals of the stigmae, e valvula +Papaver argemone: a gynoecium; +b corolla; +c stamens; +d pistil; +f anther; +g anther filaments; +h anther connective; +i anther locule; +j anther cavity; +k anther cavity apex; +l anther cavity base; +m anther cavity side; +n anther cavity tip; +o anther cavity base; +p anther cavity side; +q anther cavity tip; +r anther cavity base; +s anther cavity side; +t anther cavity tip; +u anther cavity base; +v anther cavity side; +w anther cavity tip; +x anther cavity base; +y anther cavity side; +z anther cavity tip. + +Papaver argemone: a gynoecium; +b corolla; +c stamens; +d pistil; +f anthers; +g stamen filaments; +h stamen connective; +i stamen locule; +j stamen cavity apex; +k stamen cavity base; +l stamen cavity side; +m stamen cavity tip; +n stamen cavity base; +o stamen cavity side; +p stamen cavity tip; +q stamen cavity base; +r stamen cavity side; +s stamen cavity tip. + +Papaver argemone: a gynoecium, +b corolla, +c stamens, +d pistil, +f anthers, +g stamen filaments, +h stamen connective, +i stamen locule, +j stamen cavity apex, +k stamen cavity base, +l stamen cavity side, +m stamen cavity tip, +n stamen cavity base, +o stamen cavity side, +p stamen cavity tip, +q stamen cavity base, +r stamen cavity side, +s stamen cavity tip. + +Papaver argemone: a gynoecium, +b corolla, +c stamens, +d pistil, +f anthers, +g stamen filaments, +h stamen connective, +i stamen locule, +j stamen cavity apex, +k stamen cavity base, +l stamen cavity side, +m stamen cavity tip, +n stamen cavity base, +o stamen cavity side, +p stamen cavity tip, +q stamen cavity base, +r stamen cavity side, +s stamen cavity tip. + +Papaver argemone: a gynoecium, +b corolla, +c stamens, +d pistil, +f anthers, +g stamen filaments, +h stamen connective, +i stamen locule, +j stamen cavity apex, +k stamen cavity base, +l stamen cavity side, +m stamen cavity tip, +n stamen cavity base, +o stamen cavity side, +p stamen cavity tip, +q stamen cavity base, +r stamen cavity side, +s stamen cavity tip. + +Papaver argemone: a gynoecium +b corolla +c stamens +d pistil +f anthers +g stamen filaments +h stamen connective +i stamen locule +j stamen cavity apex +k stamen cavity base +l stamen cavity side +m stamen cavity tip +n stamen cavity base +o stamen cavity side +p stamen cavity tip +q stamen cavity base +r stamen cavity side +s stamen cavity tip. + +Papaver argemone: a gynoecium +b corolla +c stamens +d pistil +f anthers +g stamen filaments +h stamen connective +i stamen locule +j stamen cavity apex +k stamen cavity base +l stamen cavity side +m stamen cavity tip +n stamen cavity base +o stamen cavity side +p stamen cavity tip +q stam... + +Papaver argemone: a gynoecium +b corolla +c... + +Papaver argemone: a gynoecium + +**BREDAUKE.** + +of the Cruciferae in having two barren calyxes, which are detached from the base upwards, and a second calyx, which is free; but there is no partition wall formed between the phloem. Of the genera of this majority of the other genera have, like Chelidonium, 2 carpels (lateral) and alter- +nating with the sepals: Fig. 383 A) and siliqua-like fruit, tim: *Euchozolzia* (Gentianaceae), with 2 carpels (lateral) and alternate with the sepals; above the placenta as above the dorsal surface of the embryo; *Glaucium* (Horn-Poppy); of the other genera, like *Crepis*, 1 carpel (median), which is produced by the formation, during ripening, of a third, sporous (false) sepals, which prevails when the valves are detached; *Saximonia* with red latex, the 2 petals being united at their bases into a tube, and the 2 sepals united into a cup; *Lobelia* (Campanulaceae) with 2 sepals and 1 capsule (median capsule) with 2 sepals and no petals—Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: Trinomia: *Triglochin* (Juncagraceae), with 2 sepals and 1 capsule (median capsule) with 2 sepals and no petals—*Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecynogea*: *Mecyno +385 + +Pollination. Papaver and Chelidonium have no honey, and are without +dolichos only visited by insects for the sake of the pollen. The other kinds +are pollinated by bees, which are attracted by the scent derived from +warm climates. **Orobanche**: Papaver semperferrum (Opium-Poppy): the laex +of its flowers is yellow; its seeds are white. **Orobanche**: Orobanche alba (Alba +many alkaloids): morphine, papaverine, nandina, thalictrum. etc. The chalazinous +seeds are also used in the manufacture of oil. Its home is in the East, where +it grows on waste ground. **Orobanche**: Orobanche ramosa (Rambler): is also +official. +Order 2. Fumaraceae (Fumarites). This order differs from the closely allied Papaveraceae in the absence of latex, a poorer +flower, generally scarcely zygomorphic (Fig. 383 D), in which one valve is usually longer than the other; the stamens are pro- +longed into a spur; the stamens are especially anomalous. Sepals +2, caducous; petals 2–2 = 2 stamens; 2 triporate; each lateral anther in bicollar (Fig. 383 A, B ; 385) ; gynecium biconcave. +The fruit is a nut or silique-like capsule. **Euphorbia**: Euphorbia - With +without stipules; without stipules; without stipules; without stipules; +generally quite glabrous and glaucous; the flowers are arranged in racemes with subending bracts, but the bracteoles are some- +times suppressed. + +**Papaver**: Papaver (Poppy) and Adonis have a doubly symmet- +rical flower, with a spur or gibbous swelling at the base of +each of the laterally-placed petals (Figs. 383 A, D). Corydalis has a zygomorphic flower, only one of the lateral petals having a spur, +and consequently they are only nocturnal because of the +bundle of stamens, which stands erect in front of the spur (Fig. +385) + +396 +395, 396 + +**CICYOTYLEDONEAE.** + +395 R. (395, 396). The fruit is a many-seeded silique-like capsule. +A peculiarity of the flower is that the plane of symmetry passes transversely through the flowers, whilst in nearly all other symmorphic flowers it lies in the middle line. In the male flowers the stamens are inserted on the upper side, ultimately becomes nearly vertical, and the spur is directed backwards.—Many species have subterranean tubers; in these the embryo germinates with one + +A, B, C—Diagram of Dioscorea (A), Gorgolida (B), and Hypoxera (C). +Fig. 395.—Diagram of Dioscorea (A), Gorgolida (B), and Hypoxera (C). + +cylindrical, which is homoeoleate and resembles a peiago-land. The tuber is in some the swollen hypocotyl (C. cirel), in others a swollen root (C. fuscace, etc.), which grows down through the precisely similar swollen root of the mother plant. The fruits are numerous, and the fruits (seeds) and capsules in the same raceme. *Fumaria* differs from *Papaveris* only by its almost drupaceous, one-seeded nut (Fig. 395). + +The structure of the flower: *Hypepium* among the Papaveraceae is the connecting link with the Fumariaceae. The diagram (Fig. 395 B) corresponds with its name, because it shows that there are four stamens instead of five of the other Papaveraceae (Fig. 391), except that there are only four stamens cells extending into the anther, while in *Hypepium* two of them are short and stamens are absent, but each of the two lateral ones are divided into three filaments, of which the central one bears a four-horned anther, and each of the + +M, N—Diagram of *Hypepium*. +Fig. 395.—*Hypepium* spatulatum: A flower (); B the same, after removal of half of one petaloid; C the same, after removal of both petals; D the same, after removal of stigma; E, the insect does this with the lower side of its abdomen, and thus rubs the stigma on the lower side of its abdomen; F, a diagram showing how it influences the direction of the prosoecus; Candiridium and Syzygium; D stigma. + +396 + +307 + +others a two-lobular (lunif.) anther. Corollaids and Fumaria stand alone in the symmetry of the flower, differing from Dicentra in having only one of the lateral petals (Fig. 395 b, p) prolonged into a spur, while in Dicentra both the petals and stamens are symmetrical, with three stamens on each side. According to Asa Gray the median stamens are absent in the last-named genus, and the lateral ones are split in a similar manner to the petals of Hyacinthus (Fig. 396 a), but this is not so (as stated by Dr. Cunliffe); i.e., that two median stamens are split, the two parts move laterally, each to its respective sides and become united with the two lateral petals, thus forming a spur. The same thing occurs in the flowers of certain umbel- +laces a close relationship to the Crucifers. A third interpretation, held by Ehrhart and others, is as follows: the median stamens are always wanting; when they appear to be present, as in Hyacinthus, it is due to the fact that the + + +A B + + +Fig. 395.--Corollaids as a flower (sympetrum); Fumaria as a flower (sympetalous). The stamens are shown shortly before the opening of the flower at the head of each petal. The stamens are seen to be united with the petiole of the flower during the visit of an insect. +side portions of the lateral stamens approach each other (as interpretable +stipulately), and thus form a spur. + +Fus. 396.--Corollaids as a flower (sympetrum); Fumaria as a flower (sympetalous). The stamens are shown shortly before the opening of the flower at the head of each petal. The stamens are seen to be united with the petiole of the flower during the visit of an insect. + +130 species; mostly from the northern temperate zones. + +POLYSELETON. Fumaria, with its inconspicuous flowers, has to a great extent been neglected by botanists. It is self-pollinated, and is dependent on cross-pollination; C. canis is even absolutely sterile with its own pollen. + +Corollaids is pollinated by insects with long proboscides (hummocks, bees), which, after visiting one flower, proceed to another and deposit their pollen on the flowers they press the exterior petals on one side (Fig. 396 c), so that the stigma, surrounded by the anthers, projects forward; the pressure of the insects, +while pressing down on the petals, causes them to spread out, thus exposing +the under-surface of the insect is covered with pollen, which is transferred by similar + +398 + +DECOTYLODENDRON. + +movements to the stigma of another (other) flower — Ornamental plants; +Dipterocarpus (Cupressaceae), Ailanthus, Corylus. + +Order 3. Cruciferae (Cruciferae). The flowers are regular, +♀; sepals 4, free (2+2), deciduous; petals 4, free, decussate, +unguiculate, placed diagonally in one wheel, and alternating with the stamens, the two median sepals (or petals) (which are vertical) +the two median split to the base) longer, placed in pairs (ternat- +niamia of Linnaeus); gynoeceum synoecious formed by 2 (as in the +previous order, lateral) carpels, with 2 parietal placentae, but +divided into 2 parts by a median groove (median septum) (septum) +(septum) (Fig. 387). Single, with a capitulum, usually two- +lobed stigma, generally commissural, that is, placed above the +parietal placenta (Fig. 387), but it may also be placed above the +dorsal stamet, or remain in the middle of the flower. The fruit is +generally a bivalve silique (Fig. 308 B, C). The valves separate +from below upwards, and leaving the placenta attached to the replum; other fruits of fruits are described below. The +only accessory organs of the gynoecium are present in the two previous orders); the embryo & cotyledon (Figs. 388 E, F; 390, 400). +—in general they are herbaceous plants. +The seeds have a testa without stipules; the inflorescence is very characteristic, namely, a raceme with the flowers aggregated together at the time of flowering into a corolla, and then opening into a bracteole-bracteole. + +Many are biennial, forming in the first year a close leaf-rotsette. By culi- +vating the tap-root can readily be induced to swell out into the form of a tuber (Turnip), or a bulb (Turnip), or a corm (Turnip), or a rhizome +very young leaves; in Cochlearia aromaticae they are fairly large triangular +scales. Siliqua hairs often occur. Floral-leaves are occasionally developed. +Ternate leaves are common in this family. The flowers are usually white, +but some have yellow flowers. Substrate (Fig. 650) is perigynous. The 3 external sepals (Fig. 651) are united at their bases; the inner one is free; there are two bracteoles enclosed within these which, however, are suppressed, and only in a few instances be traced in the young flower; the two lateral sepals are often erect and spreading; the median one is usually reflexed by the glands placed above them; they correspond in position to the external petals of the Formaceae. The 2 petals which follow mature simultaneously, and alternate with the 4 sepals; if it could be shown that these are merely of mesophyll origin, which have been deeply cut off on the two sides separated from + +BREADINE. +309 + +each other and disposed to the diagonal position, there would be a perfect +correspondence with the *Fumaceous* flower; then the petals would be followed + + +A: Achenes elongate; A transverse section; B: Collar; D: Seed; E: Embryo; F: Transverse section in regular alternation by the 2 lateral small stamens, the 3 median long stamens, +which it has been proved are split into 4 and placed in couples, and the 2 +laterally-placed carpels,—in all 6 dimerosic whorls. But the formation of the + + + +D: Transverse section of seed and embryo of *Chelidonium majus.* +Corollary of the splitting of 2 petals does not agree with the development of the +flower or base comparison, and hence the only fact in favour of this theory is + + + +E: Transverse section of seed of *Styphnolobium allarii.* + + +400 + +DICOTYLEDONES. + +the coherent prevailing correspondence with the Fumariaceae. This may be +observed that the corolla of the Fumariaceae normally closely adnate +from one protuberance and even later on may be considerably united or entirely +undivided (e.g. Fallo); in other instances they are quite distinct from the +beginning (e.g. Fumaria). The corolla of the Lepidium is similar to that of +the corolla. Lepidium ruderalis and others have no corolla. Senechium diaphanum has only 3 median stamens. Megasperma has several stamens, no doublc by +deficiency, but the stamens are very long and slender, and the filaments are +abnormally increased; *Ereptans* barbieriifolia has normally 4 sepals with +an equal number of petals and replis. It is supposed to be a variety of +Nasturtium officinale, which is a very common plant in Europe. On this +base of the stamens, are neotarsa, morphologically emergences, and not radi- +metrical annules. The presence of these neotarsa gives systematic significance, so +that the genus Nasturtium species dimorphic fruiting, *Nasturtium* *chevrolatiioides* +which has both ordinary *Cardamine* *siliqua* and 1-seeded +siliculae. + +The curved embryo appears in five forms, which have systematic importance: +1. To the Pterocarya belong those genera whose radicle (with the hypocotyl) +has bent back at its base (Figs. 600–601), e.g., *Corylus*, *Corylus*, *Corylus*, +*Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, +*Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, +*Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, +*Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, *Larix*, +*Larix*, *Larix*, *Larix*. One of the flat cotyledons (Figs. 600, 615) e.g., Hesperis, Stellaria, Lepidium. +Campanula, Campanula: O = 5. Ornamental differ from the Nasturtium in having the +sepal and petal united into a tube-like structure (Fig. 601). In the genus +Sinuca, Sinuca, Rhaponticum, etc.: O = 4—Sesleria: the radicle lies +on its side (Fig. 601). In the genus Sesleria it is supposed that a transverse +section of the seed ends there twice: Sinuca: O = 4—Drosera: the cotyledons are folded forward and backward so that a transverse section cuts them several times. +On permineration the cotyledons appear above ground as green leaves; in the Orthoclomop they are bileded, in the Lepidium- +species divided. + +1. Silicula, broad repletum (Siliculosae latipetis), valves flat or slightly valented, and the replum extends through the greatest width of the silicula (Figs. 602–604). These are situated in two rows. +O = 4—Cochlearia (Hebe-lish): the leaves are mostly glabrous herbs, generally with fleshy, stalked leaves, white flowers—Draba has an obscure, inconspicuous, somewhat compressed +silicula; hence it is considered a species of Saxifraga, most frequently with +stallike; long-stalked racemose flowers—Vaccaria: Aurinia: Laurus (Honesty): very broad and flat silicula with long stalk (the receptacle is in Cupauraceae). + +A diagram showing different types of seed structures. + +**BREDAEAE.** + +401 + +**O 1:** *Caulomelus* (Gold-of-pleasure) has a spheroid, pear-shaped silique with a small, narrow passing round joint (Fig. 402). *Subularia* (Asweld), a succulent plant with *perigynous* flower (Fig. 403) and folded cotyledons. + +**2. Silicula, narrow repletum (Siliculosa angustistipata), i.e. the fruit being narrower than the arched, more or less boat-shaped valves (Figs. 405, 406). + +**O:** *Thesium* (Penny-Cress) has a flat, almost circular silique, emarginate or cordate, with a well-developed wing round the edge (Fig. 400). *Iberis* and *Tosandra*: the racemes during flowering + +Fig. 405.—Lemna bionda. +Fruct., the valves of which +are narrow. +Fig. 406.—Osmunda aquatica. +Leucanthemum sectio through +the leaf. +Fig. 407.—Osmunda aquatica. +Fruct., the valves of which +are narrow. + +are especially corymbous, and the most external petals of the outer flowers project radially and are much larger than the other two (the flower is zygomorphic) — *Blennella*, *Meganarua*. + +**O:** *Capella* (Shepherd's-Purse) has a wingless, obcordate or triangular silique (Fig. 407). *Lepidium* (Pepperwort) has a few-(2-4) long, narrow, winged siliques, which split longitudinally into two nut-like portions; its cotyledons are folded — *Laxatia* heterocarpa ("Rose of Jericho") is an annual, illi- +culous plant, which grows up to 18 inches high; its leaves are all at first lamina branches bend together upwards, forming a kind of half; this spreads out again on coming in contact with water, and the fruits then dis- +seminate their seeds, which germinate very quickly, often in the fruit. + +Fig. 408.—Lemna bionda. +Fruct., the valves of which +are narrow. +Fig. 409.—Osmunda aquatica. +Fruct., the valves of which +are narrow. +Fig. 410.—Laxatia heterocarpa. +Flowers. + +402 + +DIOTYLEDONES. + +3. Silíqua (Siliqueous). The fruit is a true silique, several times longer than broad. The seeds in most are borne apparently in one row. + +O>>>: Brassica (Cabbage). The seeds are placed apparently in one row in each locule (Fig. 385 O); the style is long and round; the valves have only I strong, longitudinal rib.—Melanocarpus (M.) + +A diagram showing the structure of a silique with a single row of seeds. +Fig. 405.—Transverse section of a silique with broad valves, r = region; j = the valve. + +nigra, Black-mustard); the style is compressed, two-edged; the valves of the silique are one ribbed—Sinapis (Mustard); quadrangular, with three ribs—Brassica (Cabbage); the style is long and round; 3-4 strong, longitudinal ribs on the valves—Erysimum differs from Brassica by the shorter silique, broad, awl-like "beak" and seeds in two rows. + +Cucumis (Cucumber) : Cardamine (Bitter Cress) has a long, linear silique, with flat, unribbed, elastic valves. The leaves are most frequently pinnatifid or pinnate. C. pentasticha reproduces by bulbs formed in the axis of the leaves.—Arabia (Rock Cress); Matthiola (Stock); Cheiranthus cheiri (Wallflower); Barbarea (Winter Cress) + +A diagram showing the structure of a double-edged silique. +Fig. 406.—Tetracalyx ovatum. +Fig. 407.—Silícola of Capilla harenasitaria. +(double-edged, quadrangular silique). Nasturtium (N. officinale, Water-cress); the silique of the latter genus is in some species short, in others long. + +O() (400): Sinapisamum (Hedge Mustard) the valves of the silique are 3-ribbed—Erigeron; Hesperis ; Schizopetalum (with fimbriate petals). + +A diagram showing the structure of a quadrangular silique. + +**BREVIARUM.** + +403 + +**4. Fruit jointed (Lemontaceum).** The fruit is divided by transverse walls into many spaces as there are seeds, and dehisce at maturity, generally transversely, into a corresponding number of nut-like joints ("articulate-siliqua"). + +O--: Cramble (Kale, Fig. 408). The fruit has only 2 joints. The upper one is ovoid, and the lower one is oblong; the upper one is spherical, and has 1 seed.--Caulife (C. maritima, Sea-kale); the lower one is triangular, 1-loccular, the upper one more ensiform, 1-loccular (Fig. 409). + +O-->>: Rhophaea has a long siliqua, which, in the garden Radish (R. sativus), is syncarp and slightly abstricted (Fig. 411), but + +Fig. 405.—Fruit of Cramble maritima. +Fig. 406.—Oblique section of Cramble maritima. +Fig. 407.—Siliqua of Cramble maritima. +Fig. 408.—Rhophaea sativa. + +neither opens nor divides transversely (a kind of dry berry), and which in the Wild Radish (R. rhophaeum) (Fig. 410) is abstricted in its lower portion, and then divided into two nut-like joints. + +R. sativus; the "Bokali" is formed by the hypostem, after the burning of its external, corioid portions (of which there are generally two patches at the top of the stem). + +**5. Siliqua indehiscent (Nacumenaceum).** The fruit is a short, unilocular, unilocular and 1-seeded nut, and the fruit-stalks are often long, slender, and jointed. (Sometimes a thin endosperm is present)--fam. (Wood) has a few fruits in an oblong, small-winged nut (Cj) (Figs. 412, 413).--Bunius; Nodus. + +Fig. 410.—Section of Siliqua of Wild Radish rhophaeum. +Fig. 411.—Section of Siliqua of Garden Radish sativus. + +404 + +**DECOTYLUSONER** + +(The systematic division of this order given above is founded upon that of A. de Candolle. *Engler and Prantl*, Nat. Fert., 1891, adopts a some-what different system, which may briefly be summarized as follows—): + +1. **HABENARIA**. - Siligium equally developed on all sides; style divided or prolonged above the middle of the carpell, or turned back.— *Streptocarpus*. + +2. **SYNERIS**. - Siligium strongly developed above the placenta; style branched or two-leaved. + +a. **Calyculi** arising behind the bend of the embryo.— *Lepidium*. + +b. **Calyculi** arising at the bend of the embryo. + a. Only lateral members. Generally a filiform or indolentin + (filiform) form. + b. Generally a filiform, more rarely a filiform or transversely- + divided form. + c. Filiform, with a median, -- *Allionia*; *Sagittaria*; *Vallisneria*; *Brassica*; *Cardamine*. + +3. **Hair cells**, sometimes partially branched, very rarely entirely absent; glandular hairs are sometimes also present. + a. **Schizopetalum**. + b. **Hemerocallis**. - Siligium strongly developed above the placenta; style un- + divided or prolonged above the placenta into shorter or longer lobes. + a. Surface cells of the replum, not divided diagonally.— *Corydalis*; + *Ferulina*. + b. Surface cells of the replum divided diagonally.— *Malcolmia*; + *Hepatica*. + +**Foliation**. - Monotony is secured by the meristems mentioned above; but the position of the stamens is not always the most favourable for pollination by insects, because the anthers are often so long that they cannot reach insect mouth touch the anthers with one of the sides and the stigma with the other), and in many cases the anthers are too long to be obtained by insects (Cardamine pratensis) the long stamens turn their anthers outwards towards the small anther chambers, in which case both of the two large anthers to the neustria. +1500 species (180 genera), especially in +the Old World (Europe, W. Asia). Many are weeds in cultivation (e.g., *Ranunculus* composito), *Chickweed* (*Sempervivum arcanum*), Wild +Redish (*Euphorbia raphaniodes*) and others. +The following are common in cultivation: +obtained from many of the oil-containing +seeds, especially of the rape (*Brassica napus*), +and of the mustard (*Sinapis alba*). +The field-Cabbage and Cabbage. Several +are pot-herbs or fodder plants, e.g., *Cabbage* + + + + + + + + + + +
413.413.
Fus., 413.—Sativa siligium. Frutis + (Fus.) 413.—Siligium communis sec- + tion (Fig. 413).
+ +BREDAEA. 405 + +(Bredarea olcronea) with its numerous varieties: Cauliflower (caul. botryos; the entire inflorescence is usually branched and flaky), Kohlrabi (var. papyro- bates, with swollen, tuberous stem), Kale, End-Cabbage, White-Cabbage, etc.; Fr. (Fr. botryos; the whole head is usually branched and flaky); Bok Choy (Brassica rapa var. bok choy); Eruca sativa (radish from W. Asia). R. caudata (long Radish); Nasturtium officinale (Nasturtium from W. Asia); Cress (Cress from W. Asia); Crampbass (Early Crab); Crumbus maritima (Sea Kale). The seeds of the following are especially used as spices: the flower of Medicago sativa (Black-mustard), and the flowers of Carum carvi (Caraway), Carum sativum (Saffron), Carum arvensis (Horse radish), Euryt. The herbaeous parts of Cochlearia officinalis and daucus are indistinct; -- the blue dye (vendu) is extracted from Inula--Ornata--Ornithopappus, Chamaemelum nobile (White-Mentha); Mentha (Shrub); Dorea, Herpestes, Lanzanita, and others (sometimes from S. Africa). Swannianal flowers are rare. + +Order 414.--Capparidaceae (Caper). The relationship with the Cruciferae is so close that certain forms are with difficulty distinguished from each other. The difference between them consists in the number of their stamens, but it differs in the modifications which occur in the development of the stamens. +In some genera the stamens are united into a tube, in others they are separate; in some cases are divided as in the Cruciferae (6 stamens, but not interdynamous) (Fig. 414); in other genera only 3 of these; in other instances again they are divided into more than three parts; in some cases they are united into a tube, so that indefinite stamens occur (Fig. 415). The bi-carpelled gynoeceum is unilocular (without plume), but more than 3 carpels may occur. The ovary is elevated. + +Fig. 414.--Capparidaceae. +prepubescens. +Fig. 415.--Capsella biebersteinii. + +406 +DIOTTILEXOGENES. +on a stell (sometimes as much as 1 foot in length); also between the stamens and corolla a similar stalk may be found (Fig. 34). The fruit is long and ellipsoidal (Fig. 35), with a thick, hard, smooth, and a berry (Cyperus) stem absent. Some have sympphyous flowers, others have solitary calyx and perigynous flowers also occur—500 species; especially in the Tropics. The majority are annuals, but some are perennial. They offer also from the Cruciferae in having distylis species in some species. +"Capers" are the flower buds of the climbing, thorny shrub, Cyperus spinae (Fig. 45), which grow in the Mediterranean. + +Family 11. Cistiform. +The flowers in this family are perfect, regular (except Resedaceae, Fagaceae), hypogynous, the perianth-layers free (a few have them slightly united); the sepals usually imbricate; they are synstylous in this androecium, and most frequently trimerous; and generally 5-merous with Ss, Pa, A+3, G3, but other numbers also occur; several have indefinite stamens, but the stamens arise (where they do not appear to be in a regular order and are arranged, often very distinctly, in bundles) from a common base; the large number of stamens is formed by the splitting of a small number (most frequently 5); a true spiral arrangement is never found. Gynoeceum syncarpous, multicarpellate (Dilleniasceae and a few Dilleniaceae), or unisexual; the carpel is 1 or 2; the carpels 3, forming a multicarpel ovary with parietal placentation; but parallel with this, multicarpel ovaries, with the ovules placed in the inner angle of the locule, are also found, and a few genera have a free ovary, open at the top; the style is short or long; frequently persistent frame of the placenta, as in the family Rhinaceae. Half of the orders has endosperm (Violaceae, Cistaceae, Ixoreaceae), and half has no endosperm (Resedaceae, Hypericaceae, Elatinaceae, Tanacetaceae, etc.); some have a curved, the majority a straight embryo. The family is scarcely quite natural; in the future the order will probably be arranged differently. + +Order 1. Resedaceae (Mignonettes).—Herbs or small shrubs with spirally-placed leaves and very small, gland-like stipules (Fig. 46); the hypanthium is cup-shaped or more or less merged; and arranged on one axis typically without bracteoles. The syngynomephoric structure is produced by the greater development of the posterior side of the flower, especially the petal and the nectary ("disc," in Fig. 416 d) which is situated between + +**CHITOFOR.** 407 + +The petals and stamens; in general there are 5-8 free sepals and petals, the latter consisting of a large scale-like sheath with a fimbriated blade (see Fig. I); stamens numerou- +ous; carpels 6-2 united together by ovary base, becoming loculicidally dehiscent, but the cavity of the ovary is not closed at the top. In *Astro- +carpus* the gynoeceum is syncarpous. The fruit is most frequently a capsule; the seeds are roundish without endosperm, and the embryo is curved. + +This order connects the Rhodantheae with the Chitofor- +ium. It is closely allied to the Rhodanthea by its entire calyx, its parietal placentation, structure of the seeds, the inflorescence, etc., whilst by the irregular flowers and the fine plumose at the posterior side of the flower, it differs from that order. The flowers are long lasting, being its characteristic number (2-4) and by the very different mode of dehiscence of the fruit. The fruit is usually a capsule, which is seen in the fact that the number of the perianth-leaves is not constant. 5 in *Rinza* +necula both the calyx and corolla appear to be a flower, because the posterior part of the corolla is prolonged into a plumose appendage. With 3-10 +stamens, they stand in 1 whorl, i.e. front in the ovule and petals; if there +are several, their position depends upon the splitting...*Astrocarpus* is remark- +ably syncarpous fruit and the position of the ovules on the internal surface +of the ovary. + +The yellow, flat disc at the back of the flower serves as a nectary, the honey +being produced by insects. In some species this nectary is not +effected, then self-pollination may take place, at least in *F. advena.* +As specific; the majority in the Mediterranean and in Persia. +*Rinza advena* (L.) Rchb. f. (Fig. II.) A plant of 1-2 feet high. The *Tyrus* +*West* 1 yields a yellow dye. + +Order 2. *Droseraceæ* (Sundews). Herbs, chiefly living on moist or in water, and with leaves adapted to catch and digest insects. With regard to their structure they are closely +allied to the Violaceae, especially to those with regular flowers. +*Drosera* (Sundew) has a long-stalked accordial cyme with regular, +q., hypogynous flowers. 5-mers in *S. filifolia* (Fig. III.), P.S., P.S., G3 +(Grass), etc., with free or partly united sepals (ovular or +partially-placed ovoids in the unilocular ovaries). The capsule opens also as in *Ficoid*, but, among other differences, the styles are free from each other; in *S. rotundifolia* a leafy winging thallus. +*Rimora* has radials, long-stalked leaves, with a blade (Fig. III.) +covered by numerous strong glandular hairs, placed on edge in +the middle; when small animals are caught by these hairs, the latter and the entire + +Fig. 407—Diagram of Rinza advena. + +408 + +DICOFTYLEDONES. + +blade close alwayy over them dissolving and absorbing all the digestible matter as nourishment. +*Drepanum* *carnifex* (Fig. 417 ; N. Am.) has the same appearance as *Drepana*, but the leaves are constructed as in Fig. 418. The stalk is flat and winged, the blade small, circular, with powerful, pointed teeth along the edge, and on its + +![image](https://i.imgur.com/3Q5Z5.png) + +Fig. 417.—Lengths of Drepanum refugialis (nat. size), and a leaf (magnified). + +surface are 6 small bristles ($z$), which are very sensitive. When these are touched, the animal immediately withdraws into its body, which is long and coiled, imprisoning the irritating object, the teeth round the edges fitting like the teeth of a trap. If it happens to be an insect or similar body, a digestive fluid is secreted within the body, which dissolves it, and the animal swallows it. *Ameles* *carinata* *vulcanica* (Central and S. Europe) captures small aquatic animals in a similar manner, but does not imprison them. The lower halves of its leaves also close when irritated (Fig. 419).—Drepanodesmus. + +About 110 species ; most of them in the temperate regions. + +Orders 2 and 4. *Sarracenium* and *Nepenthaceae.* These two orders are perhaps most remarkable for their mode of life, with those among other things, in the manner of taking nourishment. Like the Drepanum they absorb their nourishment from dissolved animal matter by means of their leaves, which are especially constructed both to catch, to retain, and to digest any small + +![image](https://i.imgur.com/3Q5Z5.png) + +Fig. 418.—Drepanum carinatum. Leaves (nat. size). + +1 + +CISTILORE. +409 +animals which may be caught. The *Sarracenia* are North American marsh-plants (10 species) which have pitcher-like leaf-stalks, in the cavity of which a fluid (with properties approaching those of gastric juice) is secreted. + +A +B + +Fig. 68. —*Sarracenia* *nobilis*, a plant (pan. cir.). B Leaf (top); the blade is closed; the winged stalk is prolonged into a 4-lobed stem. + +and which bear at the apex a small, tubular bladder; these leaf-stalks are the enchythic and digestive organs. —*Sarracenia*, Duriatonia. + +C +D + +Fig. 69. —*Sprekelia* (*enfused*). + +*Nerteraceae* has only one genus, *Nertera* (the Pitcher-plant), about 35 species, all tropical, with a tubular leaf-stalk, and a large, tubular bladder. The leaf-stalks are twining organs, and terminate either simply in a tendril, or in addition to this, with a pitcher-shaped body (which in some species may be + +410 + +DICOTYLEDONES. + +as much as a foot in length) on whose upper edge a lid-like structure is found (Fig. 420). In this pitcher, as among the Saracenmaceae, a fluid is secreted which is able to digest the animals captured (sometimes rather large) and which corresponds with the juice of the pitcher-plant. + +Order 5. Violaceae (Violets). The flowers are 3-petalled, and generally zygomorphic, hypogynous, with Ss, Ps, A5, G3 (Fig. 421). The stamens are closely applied to the ovary, they have a very short filament, and at their summit generally a membranous appendage formed by the prolongation of the connective (Fig. 422 g). The corolla is unisexual with 3 partial pinacate; style + +
A diagram of Viola.
+
The large-leaved form of Viola odorata; A the flower in median longitudinal section; B the gynostemium.
+ +unisexual. The fruit is usually a 3-valved capsule, opening along the dorsal sutures (Fig. 428). Embryo straight; endocarp fleshy (Fig. 425)—Many are herbaceous plants (e.g. *Viola*), but in the Tropics shrubs are also found (e.g. *Jonquilum*); a few are trees; the leaves are scattered, with stipules, and involucre present. + +*Viola*. The sepals are prolonged backwards beyond the point of insertion (appendiculate); the corolla is polypetalous, descending incurvate, and zygomorphic; its anterior petal being larger than the others and often purple; the posterior petal is white or yellow; the 3 almost sessile stamens are provided with a spur-like nectary, which protrudes a considerable distance into the petaloid spur (Figs. 421, 422 u, op). The style is club-like, and bears the + +CISTILOPEL. 411 + +stigma in a groove on the anterior side (Fig. 422 z). Herbs with chironomus, or anemones flowers, F. odorata, comia, etc., have cleistogamous flowers which produce fruit in addition to the large, coloured (red, yellow, white) petals. These flowers are pollinated by insects, but not by insect pollination, and also smaller, less conspicuous ones designed for self-pollina- +tion. The stigma, as in Fig. 423 d, st., and Bt, is situated on the anterior side of the flower (Fig. 423 b), and the style is long and slender (Fig. 423 c). The stigma is covered with a sticky substance (pollen) which adheres to the spur (ypt); below it is situated a valve, easily covered with pollen when the proboscis of an insect is introduced into the spur, but which closes upon its withdrawal. In this way the pollen is carried away by the insect. The fertile +is visited by the honey-bee, which insures cross-pollination, and in the absence of bees it effects a self-pollination. The flowers are visited by other insects, +such as flies, bees, and spiders; var. rugosa, is less frequently visited by +insects (bumble-bees). In F. silvestica and F. comia the pollen is carried on + +Illustration of a flower with a long style and a sticky stigma. +Fig. 423.—Capitule after detachment (pan. stat.), Fig. 423 b.—External view of the seed. +Fig. 423 c.—Stigma with attached pollen grains. +Fig. 423 d.—Head or proboscis of the honey-smoking bee.—The fruits of F. odorata bury themselves slightly in the soil. In the others the fruits are raised above the ground by means of a stalk (pedicel), which is produced from the base of the calyx and ejects the seeds, one by one, with much violence, so that they are thrown to a great distance. + +The genus-Group has regular or almost regular flowers. Gampolamptus +ocellata are found in Papua-guinea. Some species diffuse the most by the regular ocella, and are free or united stamens. + +Order 5. Liliaceae—The Liliaceae-species are used as +Ipecacuanha. A number of Fimia-species are cultivated as garden plants, +especially F. odorata (see-scented Violet) and F. tricolor, which have a large number of varieties. + +Order 6. Frankeniaceae—A small order with doubtful relationships, +Fraxinus is a tree with compound leaves and small flowers in axillary spikes, +petals free. Uniohouni occurs, with 8-4 per leafed phloretes. Fruit: A cupule. +Embry: short, endospermous Especially in S. Europe, Africa, on the +other hand: in North America. + +Order 7. Tamaricaceae (Tamarisk). To this order belong only Tamarix +and Myricaria. They are shrubs of a cryptus- or heather-like appearance, as + +412 + +DISCOTYLEDONES. + +the scattered leaves are very small, sessile, scale-like or linear, adpressed, entire, and usually glaucous, and the branches are slender and white-like. +The flowers are borne in small spikes or racemes, and are small, roundish or whitish, regular, 5-merous, with 5 sepals and 5 petals (sometimes 6), the sepals (which often has stipules at the base of the filaments), or A+3–5 (Myricaria, in which the stamens are united at the base); the number 4 may appear instead of 5, but in this case the stamens are free. The calyx is tubular or campanulate, which is lobed and has either partial placenta (Myricaria) or a small basal placentation (Loranthus). The corolla is regular, 5-merous, with 5 petals, which are often hairy, and resembling the Willow in having a tubular corolla over with numerous stamens; and the seed-wood in this case is borne on the chalaza, and may be found in the winter—40 species; North Temperate, on the sea-shores or steppe, especially in Asia. Ornamental shrubs Myricaria porronis, and *Loranthus* politus. + +Order 8. **Chloranthaceae**. Shrubs or herbs, natives especially of the Mediterranean region. Flowers generally in raceme-like scrophoid cymes, regular, 5-, hypogynous; sepals 5, free, twisted in the bud, of which the two outer are generally much smaller than the others; petals 5, free, twisted in the bud (in the direction opposite to that of the sepals), or sometimes united; gynoecium syncarpous; carpels usually 3-5-styles; style primary uniramous along with parietal placentaion (seldom divided into local, with axile pla- +centation). The ovaries are orthocarpic in opposition to some of the other orders of this family. The capsule dehisces alone along the dorsal axis of the ovary. The seeds are small and provided, +generally opposite and stipulate.—They are Violaceae with regular flowers, +numerous stamens and curved ovule. The numerous stamens are as realy only one or two per flower; but when they are formed together they are formed, therefore, in descending order, like the lobes of many compound foliage-leaves. + +*Helianthemum* (Rock-Rose), has 3 carpels.—*Cistus* has 5 (~10) +carpels. + +About 70 species ; temperate climate, especially about the Mediterranean. +The root of the *Cistus*-species has been used medicinally (adoumum). +Order 9. **Bixaceae**. This order is closely allied to the Cistaceae and Loranthaceae. The flowers are regular, 5-merous; sepals numerous stamens, unilocular and parietal placentaion; sometimes uni- +cyclic flowers; it differs in having anisocarpous cymes, in the initiation of the ovule, by being a perennial herbaceous plant with simple leaves; which usually have stipules, and are occasionally dotted with +pubescence. The seeds are small and stipulate. Of the known species it has a 3-celled capsule; the seeds are enclosed in a shiny red, bony testa, +which contains the well-known orange or yellow dye; annatto. + +A diagram showing a flower structure. + +CUSTELELLUS. 413 + +Order 10. Dilleniaceae. Gymnosperms usually sporophytes, and arborescent. +The flower has most frequently 5-35, and less frequent (stamens or more +handled) sometimes irregular, 200 species ; tropical woody plants, many +laxer.-Dilleniaceae. Anacardiaceae. Anacardium, Ziziphus, etc. + +Order 11. Elateraceae. (Water-lilies). About 35 species belong to this order; especially in temperate climates. They are small, creeping, rootless, +annuals, with a single leaf, and a short stem. The flowers are solitary or situated in small dichasia in the leaf-sap; they are small, +regular, 5, hypogynous, with free petals, the same number in all 5-8 hours +of the day; the stamens 5-6, inserted on the corolla-base; the calyx 5-6 (Lycra- +piper), or 5-merous (Berger); the corolla-stamens are sometimes supressed; +petals imbricate without being twisted; the coryle is 3-4-5-leaved, with 3-4-5 +petals; the fruit is a capsule, which is often transversely ribbed, endocarpus wanting. +The order is most +nearly allied to Hypericaceae, whose primitive form it appears to represent. + +Order 12. Hypericaceae (St. John's-worts). This order is recognised by its always opposite or verticillate, simple and +edible leaves; the flowers regular, hypogynous, sessile or short-pedicelled, dotted +with peltate glands; by the always 7-regular, hypogynous flowers +in a cymose inflorescence; the generally 5-merous calyx and corolla, with sepals and petals free; the stamina 3-5, uniseriately arranged (Fig. 427); the fruit is a capsule or berry; the style is free, +styles usually free. The coryle is 3-5-leaved, or unilocular with +3-5 parietal placentae. Fruit a capsule (dehiscing septically) or +berry. Endocarpus absent. + +The inflorescence is a dichasium or helicoid cyme. The structure of +the flower is the same as that of the preceding order : SS : PS ; antherules these +are none among are two sericeous wheels of stamens in regular alternation, of + +A diagram showing the arrangement of flowers in a hypericaceous plant. +Fig. 426.—Diagram of Hypericum pseudomontanum. +Order 12. Hypericaceae (St. John's-worts). + +Fig. 427.—Hypericum Flower with three sepals and three petals. +SS : PS + +414 + +**Dicotyledons** + +which the inner is cyclopedous, but the outer whorl is only represented by 5 small scales (Fig. 427), or in altogether absent (Hypogynum calyculatum, I. hirundinaceum), and the inner divided into numerous stamens, that in these stamens are so deeply divided that they appear to be lobed (Fig. 428, 429, 430) (see also the Gasteria). In other cases the flower becomes 3-merous after the petals, stamens 3-8 following in regular alternation (Figs. 426, 427), the outer whorl of stamens in some cases being reduced to one (Fig. 428), or may be together suppressed. Carpels 3-5. The petals are very reduced in the bud, and are then oblique. + +**Hygrocarpus.** Some species have a square stem; in these cases the leaves are placed opposite the edges. Fruit: a capsule. -- *Tussica* has a berry--The flowers of Hypogynum have no honey, and supply only pollen; otherwise they are similar to those of *Caryophyllus*. About 240 species; the trampel ones being often shrubs or trees; the others generally growing in meadows and woods. The leaves contain a mucilage, real malt, which can be extracted with alcohol. The Amaryllidaceae, the dried sap of species of *Ficus*. + +**Oleteria.* The genus is very rare in Europe. Clamitif ally allied to the Hygrocarpinae and Tormentosaceae. Leaves opposite or verticillate. Tilia flowers are often unisexual; stamens united; the gynoecium has most frequently a sessile, radiating or spreading ovary. --About 100 species; chiefly in the Tropeae (Am.). They are principally woody plants and their bark contains a yellow gum resin, "podophyllum," which is extracted from *Gentiana lutea*, and used as a remedy for dropsy. *Rosa* spinosa, *Rosa* damascena, and *Mimosas* (W. Insk.), have very delicious fruits. To this order also belong *Platanus* triandra, *Pentasaceae* bryocarpa (the Butter-bush), *Chamaecytisus*, *Cytisus*, etc. + +**Order 14.** **Terrestrialiaceae.** Trees and shrubs with scotophylls, or leaves with stipules; the flowers regular, pentamerous or without stipules (Fig. 429). The most important genera are: *Ceratium*, and the closely allied *Thorn* (by some authors these are united into one genus). The flowers are regular, hypogynous, and situated singly on very short stalks. A number of stamens is usually present; the filaments gradually pass over into the sepals, and the leaves (3-5) of the calyx again gradually pass over into the corolla (this being especially marked in *Ceratium*), of which the number of leaves varies (5, 6, 7 and upwards); in some cases there is a median leaflet; the petals are slightly united at the base; stamens numerous in many whorls, the external ones are arranged in bundles and united with the petals as in the Coleiflorinae; gynoecium synapocarpous; style often free nearly to the base; ovary 3-celled; ovules numerous in each locule. The fruit is a woody capsule. + +A diagram showing a flower with five petals and three stamens. + +**CISTIFLORE.** + +—Other genera show more distinctly than the same structure as in the preceding orders, namely : 85, F6, A5-5, of which the only stamens are often suppressed, and the petal-stamens divided into numerous stamens.—*Kielmeyera* (p. 307). + +200 species ; especially in the Tropes (E. Asia, Am.). The leaves of *Thos chinensis* (or *Canclia thoe*), the Tex-tree (E. Asia), are cultivated for the wood, and also for their flowers, which are yellow, with many leaves, of greyish colour; there are many varieties. Ornamental plants. + +*Canclia japonica* and *Aetnoidia*. + +Fig. 48.—*Thos chinensis* (Fedr.) + +Closely allied to this order are: Order 15. Rhinoboleae (with enormously large hypostylus—hence the name), and Order 16. Maracavioaceae (partly epiphytes, with dimorphic leaves and cup- or helmet-like, coloured, honey-scented flowers).—Order 17. Dipterocarpaceae. This order has taken its name from the large wings attached to the fruits in Dipterocarpeae (the wings being largely developed on some trees and shrubs from E. Asia). 200 species. One genus newly proposed is found in the stem of *Dryopteris caudata*. Home ; *Fertilis.* + +W. D. +E E + +416 +**Erythyleaeae.** +Family 12. *Guineales.* + +The flowers are hypogynous, 5-, polygamous, usually regular (except *Federowiczia*), with 5 sepals (5-merous) and throughout 5-merous: S5, P5, A5+5 or 5 or 0+5, G5 (quintupletal). The stamens soon fall off and are ephelidiothecous, often united at the base (monadelphus); the corolla-stamens are in some completely suppressed (e.g. *Bauhinia*), in others reduced to teeth (Lauraceae, Fig. 431), or in some free (e.g. *Erodium*, *Tropaeolum*), and only 5 stamens (Fig. 431). Rimp-like nekaries are not pre- +sent, but at most only glandular bodies, borne outside the base of the stamens. Ovaries many-locular. The ovaries as a rule are pendulous, with a short style inserted into the ovary (Fig. 431, J), +and the radicles therefore also point outwards. Usually herba. +Related to the *Colimiferaeum.* + +Order 1. *Oxalidaceae.* Most of the species are herbs with rhizomes; the leaves are stalked, compound, with entire leaflets which are folded and bent backwards in the bud (and in the sleep position), ex- +stipulate: some species have sensitive leaves. + +The flowers are regular or in dichasia, and unisexual or bisexual. The perianth is effaced by the petals, or is short, medium- or long-cyced (Fig. 432). And some, e.g., *O. oxaloides*, have cistostigmatic diarses in a calyx-like tube. The stamens are free or united at the base of the corolla-stamens or of all the stamens. O. oxaloides and others have adventitious outer petals, reticulating taproots.—Averrhoa is a tropical tree, with berries like plums. + +285 species (205 belong to *Guinalea*); chiefly in Afric and Trop. America. +—Oxalis of potash is contained in the leaves of *Oxalis.* + +Fig. 432.—Diagram of Oxalis oxaloides. + +ORDINE 2. LINACEAE. +Herbs with scattered or opposite, sessile, simple, small, entire leaves, without (nearly with small) stipules. +The flowers (Fig. 430) are regular, hypogynous ; the sepals are free, twisted, quickly falling off. Stamens united at the base ; the petal-stamens are either reduced to teeth (Fig. 431 A, m) or entirely enpseudosed. Styles free. The (3-5) epipetalous loculi of the ovary are incompletely halved by false divisional walls, each half. + + +A: A flower showing the petals and stamens. +B: A longitudinal section of the ovary. +C: A transverse section of the capsule. +D: A longitudinal section of seed. +E: A transverse section of seed. +F: A transverse section of seed. +G: A transverse section of seed. +H: A transverse section of seed. +I: A transverse section of seed. +J: A transverse section of seed. +K: A transverse section of seed. +L: A transverse section of seed. +M: A transverse section of seed. +N: A transverse section of seed. +O: A transverse section of seed. +P: A transverse section of seed. +Q: A transverse section of seed. +R: A transverse section of seed. +S: A transverse section of seed. +T: A transverse section of seed. +U: A transverse section of seed. +V: A transverse section of seed. +W: A transverse section of seed. +X: A transverse section of seed. +Y: A transverse section of seed. +Z: A transverse section of seed. +AA: A transverse section of seed. +BB: A transverse section of seed. +CC: A transverse section of seed. +DD: A transverse section of seed. +EE: A transverse section of seed. +FF: A transverse section of seed. +GG: A transverse section of seed. +HH: A transverse section of seed. +II: A transverse section of seed. +JJ: A transverse section of seed. +KK: A transverse section of seed. +LL: A transverse section of seed. +MM: A transverse section of seed. +NN: A transverse section of seed. +OO: A transverse section of seed. +PP: A transverse section of seed. +QQ: A transverse section of seed. +RR: A transverse section of seed. +SS: A transverse section of seed. +TT: A transverse section of seed. +UU: A transverse section of seed. +VV: A transverse section of seed. +WW: A transverse section of seed. +XX: A transverse section of seed. +YY: A transverse section of seed. +ZZ: A transverse section of seed. +AAAAA: A transverse section of seed. +BBBBB: A transverse section of seed. +CCCCC: A transverse section of seed. +DDDDD: A transverse section of seed. +EEEEEE: A transverse section of seed. +FFFFF: A transverse section of seed. +GGGGG: A transverse section of seed. +HHHHH: A transverse section of seed. +IIIII: A transverse section of seed. +JJJJJ: A transverse section of seed. +KKKKK: A transverse section of seed. +LLLLL: A transverse section of seed. +MMMMM: A transverse section of seed. +NNNNN: A transverse section of seed. +OOOOO: A transverse section of seed. +PPPPP: A transverse section of seed. +QQQQQ: A transverse section of seed. +RRRRR: A transverse section of seed. + +Fig. 430.—The flat plant. + +A. The perianth : a, segmentum ; b, segmentum ; c, petal-stamen reduced to tooth. B Longitudinal sections of ovary. C Transversal sections of capsule. + +Fig. 431.—Capsule (see text). + +A. Transversal sections : a, a longitudinal portion ; b, the cotyledons ; c, the endosperm ; d, the radicle ; f, the endosperm ; g, all the parts. + +contains one ovule (Fig. 431 G). The fruit is a spherical capsule, delating along the divisional wall (Fig. 432); the 10 (-8) seeds have a straight embryo and very slight endosperm (Fig. 433). + +417 + +**418** + +**DICOTYLEDONS.** + +*Linum* (Flax) has 5-merous flowers. The main axis terminates in a flower; and the succeeding branching is epipetalous, or unifoliate scapular branching by unilateral development, and the flowers in consequence of the epigynous symmetry of the corolla, are all alike. The lower bract, or sheath, assumes a position apparently lateral (i.e. racemose) without bracts; each branch of the symposium generally has 2 leaves. The upper bract is usually persistent, and the lower one, which is a leafy layer becomes meridional in water.—Bastardia has a 4-merous flower. It is a small herb with opposite leaves, and regular, dichasial branching. + +The anthoc and stigma in *L.* catharticus and *Ustilago* develop simultaneously, and cross-pollination as well as self-pollination takes place. *L.* grandiflorus, porcaceae, and others, are dioecious (short- and long-styled). Three are known to be hermaphrodite. + +130 species; *Linnæus* and *Borée* are male genera.—*L.* undulataeum is exten- +sively cultivated in Europe (especially in Russia and Belgium). N. American and elsewhere are also cultivated. *L.* alba is a garden plant. The seeds contain linseed oil, which is extracted from the seeds, and partly on account of the softness of the stem, which has very thick-walled cells. The seeds and oil are optical. The species cultivated for this purpose was a diploecious plant. Floral species are cultivated as ornamental plants. + +Order 3. **Geraniaceae.** The majority are herbs with dichasial branching, and scattered or opposite, stalked, palerinued (rarely penicillined) leaves with linear stipules. All the flowers are perfect (except *Dentaria*), excepting 10 or 9 stamens which are slightly united at the base. Nectaries alternate with the corolla-stamens. The anther is mostly frequently 5-lobed, deeply 3-grooved, and bears 1 well-developed style (a "bank"), which towards the apex is often forked into two branches, one of which is free, the other locular, pendulous or ascending. The carpels become detached from one another when ripe, and bend or roll back (Fig. 454) or become spirally twisted in the upper part (bank-like) part (Figs. 453, 456). The fruit is a capsule; the calyx remains attached to the carpel, in consequence, remains either closed, and the fruit is a 5-merous schizocarp whose nut-like lower portion, containing the seed, is forced into the ground, thus burying the seed by the movement of the soil. The seeds are usually winged (Fig. 457). (*Caryophyllus*, Fig. 453); or it opens along the ventral suture, so that the seeds may fall out, and it is then a 2-valved capsule, with septal de- +hiscence (Fig. 458); and the rolling up often takes place so audibly as to render that part of the ground shot out to considerable distances. The embryo is usually green and carpellate, and the nucellus folded ; endosperm is wanting. + +A diagram showing the structure of a dicotyledonous flower. + +**Goranaeeae.** 419 + +*Goranae* (Crane's-bill) has ±5-8 stamens, and a septicidal capsule; the carpels most frequently remain suspended from the apex of the column (Fig. 434). The leaves are most frequently palmerised. +The flowers are usually solitary, sessile, or peduncled (2-3 mm. sec- +pierced cyme). — *Erodium* (crane's-bill); inflorescence a many- +flowered unipared scorioid cyme, stamens 5-0 (petal-stamens are wanting), and fruit a schizocarp whose carpels become detached; the latter are often scattered on the ground, and the plant is anemoneless spirally (Fig. 435). +The umbellate inflorescences are composed of multiflowered scorioid cymes. +—the most primitive type is represented by *Biebersteinia* : S. P., As. t.-t. 65 +(ovate leaf, and sterile, white flowers); S. P. 2 small-flowered species with advanced +type of *Erodium*, which has symmetrical flowers, the posterior sepal being +Fig. 434 - Goranaea sen. +Fig. 435 - Erodium corymbosum. + +**Fam. 43.—Petrocarpaceae.** Petrolanthus, *Petrorhagia*. Fruit (1). + +prolonged into a spur which becomes adnate to the pedicel; the petals are wanting, and the stamens are often wanting. (*Erodium* may be slightly xeromorphic). + +**POLYANTHACEAE.** The large-flowered *Goranaea*-species are prebundiculæ, e.g. +*Goranaea* (crane's-bill); the flowers are sessile, with a long spur which ex- +ceeds these the stigma, after shedding the pollen the stamens bend out- +wardly ; the small-flowered are also adapted, with various modifications for +the wind-pollination of the flowers (e.g., *Erodium*).—See *Petrorhagia*. +—Several *Petrorhagia*-species, with numerous varieties, are ornamental plants +(from S. Africa). + +**Order 4.—Tropaceae.** Herbacous, juicy plants which have +scattered, long-stalked, petalate leaves without stipules, and often + +420 + +DICYCTYLEDONAE. + +climb by their sensitive petioles. The flowers are situated singly in the axils of the foliaceous-leaves on long stalks, and are **zygomorphic**, the receptacle being at the base of the spur being pro- +longed here to a short stalk. There are also differences between the upper and anterior petals, the 2 posterior petals situated on the border of the spur being perigynous, and the edge of the lower one being fringed. After the 5 sepals (which are more or less coloured) and the 5 petals, follow 8 stamens (as the 2 median ones are suppressed, one from each whorl) and a pistil with a single ovary. The fruit is a **schizocarp** of the 3-lobed ovary in 1 ovule. The fruit is a schizocarp and divides into 3 lozened, drop-like fruits, which are attached to a short, often pronounced column beneath them. Endo- +spern is wanting. The cotyledons are thick and sometimes slightly coenocytic. +Tubers often occur. + +*Trigonium* (Fig. 47).—The genus is cosmopolitan. All from America. + +*Trigonium* (Fig. 47).—The spur is the receptacle for the nectar; the flowers are protandrous; the anthers open first, and one by one take up a position in front of the entrance to the spur, remaining their original position when the pollen is shed; thus they are said to be "anther-synchronous." These plants have an aerial thence (hence the name "Naturistum," "Indian Grass"), on which account the flower-buds and young fruits of T. +*Trigonium* are used as syrups. Some species are ornamental plants. + +Order *Balsaminaceae*. Herbs or shrubs, annual plants with pearly, white or greenish stems, so transverse that the vascular bundles may be distinctly seen. The leaves are simple, usually scattered, penninerved and dentate; stipules are wanting, but sometimes large glands are present in their place at the base of the petioles. The flowers are zygomorphic, regular, with 5 sepals, 5 petals, whereof the petal-stamens are suppressed (S5, P5, A5+0, G5); the sepals are coloured, the 2 anterior ones are very small or entirely suppressed; the posterior one is very large and drooping; the stamens are numerous; in some species sometimes the weight of the spur turns the flower completely round, so that the posterior leaves assume an anterior posi- +tion; apparently only 3 petals, since the lateral and the pos- +terior petals become united in pairs, and the anterior is larger + +Fig. 47.—Diagram of Trigonium: spur. +1 + +**COLUMNIFERE.** 421 + +and differently shaped; the 5 stamens have very short and thick filaments united at the base, and their anthers finally adhere together and remain in this condition, covering over the gynoecium; the filaments ultimately become thin, the base and entire anthers are raised on the apex of the gynoecium as it grows up. +The gynoecium has a sessile stigma and a 5-lobular ovary. The fruit is a capsule which, on maturity, opens suddenly when erected, shedding into valves from the base upwards, and as the 5 valves fall away, they leave behind them a short columna to considerable distances ; a central columna persists (fig. 430). The embryo is straight, and without endosperm. + +Inopinatae: in Europe only L. *mollis*—235 species; especially from Asia. Several species have two kinds of flowers: small, ditogamous, but fertile; + +Fig. 430.—Diagram of Inopinatae glabella. +Fig. 430.—Fruit of Inopinatae. + +and large, coloured flowers, which in L. *blandoides* (ornamental plant, E. Ind.) are protandrous and pollinated by hive-and-humming-bees, as they suck the honey from the flower. + +Order 6. *Linnanthaceae.* The flowers are regular and differ from all the other orders in the family by having the corolla not in front of the petals, but in front of the stamens; the stamens are free, or nearly so, and often with a common appendage; the ovaries are axillary and epigynous (anatropous with ventral raphe). The fruit is a silique, with much or no coat. —*Linnanthus* 8 species; N. Am. perhaps belongs to another family. + +Order 7. *Humaceae.* Trees and shrubs; about 20 species; Trop. Am. + +Family 13. *Columnifere.* + +The chief characteristics of the orders belonging to this family are the $V$, regular, generally 5-meronous, appressed flowers with + +402 + +**Dioctylodessee** + +5-merous calyx, sepals united and valvate in the bud; petals 5, free (often fused in the bud); stamens e.g. p. 10, in two whorls, but one of these is more or less suppressed, often altogether wanting, +or only represented by a few filaments after (more rarely) to generally divided more or less deeply into a long column of anthocyanin-bearing filaments. The filaments too (except *Tulipus*) are united into a tube, which, especially in the Malacose, forms a long column in the ovary (Fig. 443). In the *Cotoneaster* (Fig. 446, 448), in this case, which is the most pronounced, the filaments are united into one bundle (monadelphous), in other instances, polyadelphous. The number of carpels varies greatly (2 to about 50), but they are usually always numerous in a syncarpous multicellular gynoeceum. The ovules are always numerous and the ovaries are always scattered and generally stipulate. All the green portions very often bear stellate hairs, and the bark in all the 3 orders is rich in tough base. The leaves are deciduous in the *Cotoneaster*, from which it is very hard to draw a sharp line of demarcation, and it is also allied to the *Cotoneaster* and to the *Granadilla*. + +Order I. **Sterculiaceae** (including *Sterculia*). + +This is no doubt, the order of plants with which the stamens occur undivided. Oedipodostemonus. The 10 stamens in two whorls are most frequently united at the base into a short tube, and have 4-lobular, extrorse anthers. The calyx-stamens are nearly always simple, but sometimes divided into several segments; the petals are entirely suppressed. The same relation is found, for instance, in the *Ampelidaceae* and *Rhamnaceae*, namely 5 stamens in front of the 3 petals, not infrequently the 3 stamens are doubled (Fig. 413). In *Hibiscus* (Fig. 414) there are 5 stamens. + +The corolla is often wanting, or developed in an unusual manner. +Each locule of the ovary (generally 5) always contains more than one ovule. Fruit a capsule. Androecyphonous often present (*Hibiscus*). + +Herpaniaea, *Makrocaria*, *Melochia*, etc., have flat pistils with twisted valvatae; 5 undivided stamens, which usually are but slightly united at the base, and most frequently without Staminae. *Thamnacis*: *Helicteres*: Sterculiae (free follicles), *Strychnos*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: *Elaeagnus*: **Fig. 440** bears large, reddish-yellow, berry-like fruits, resembling short cumu- + +COLUMNIFERA. 423 + +bears, but ultimately becoming leathery to woody; in each of the 8 loculi are +2 (apparently only) rows of horizontal, oily seeds, as large as almonds. +Caryophyllus large, thick, and irregularly folded. Endosperm absent (Fig. 449). +Of the 500 species of this genus, 17 are found in the United States. The species +none in Europe or in N. Asia.—The seeds of the Cocoa-tree (*C. cacao, blader, +plumeria, etc., natives of Trop. Am., especially north of the Equator) are + +Fig. 449.—Theobroma cacao. Branch with flowers and fruits (2). +cat. + +Fig. 451.—Theobroma cacao. +B + +Fig. 451-453.—Theobroma cacao. +A +B + +Fig. 451.—Diagram of the flower of *barren stamens.* +Fig. 452.—Section in transverse section ; a bilium. A bilium after the removal of one +of the cylostomata. + +used for chocolate and are also official ("Cocoa-beans," "Cocoa-butter," +"Oil of Theobroma"). Theobromine Cide arnandina, African +"coffee." The seeds of the cocoa-tree belong to the orders of the +Columniifera chiefly in the stamens being entirely free from each +other, and also divided into many flaments, as far as the base, or at +all events very far down, so that the flower appears to have numer- + +411 + +624 + +**Dicotyledones.** + +one stamen or to be slightly polyandrous (Fig. 443); in addition to this, it may be observed that the anthers are 4-celled and introrse. In *Lobelia* the groups of stamens alternate with the petals (Fig. 445). In *Cerastium* (Cerastium fruticosum) 10 free and single stamens are found in 2 whorls, while in *Lobelia* the groups of free stamens in separate bundles. The stamens are more or less united in *Aponogeton*. Style simple. Ovary 2-lobular. The ovaries are pendulous, and the style is long. The calyx readily falls off; the activation of the entirely free petal is slightly imbricate (not coriaceous). + +*Tilia* (Figs. 443, 444). Calyx and corolla 5-merous; the 5 staminal leaves (opposite the petals) are united into a large number of stamens which are free or united into groups; gynaeceum with 5 (rarely 6) ovules in each locule; the ovary ripens into a 1-seeded nut, which is not detached from the base of the inflorescence but is carried away by the wind, whirling round and round, its large-winged seeds being held in a parachute (Fig. 443). Only trees, with an alternation of heart-shaped and dentate leaves, are known in the other Cuculiferales, are often present. The terminal bud of the inflorescence is sessile, and when the growth is then continued symmetrical by the uppermost axillary bud. The inflorescence (Fig. 443, 444), which is developed in the axil of a foliage-leaf (Fig. 444). The first six 2 bractlets (a, b) are large, thin, leaf-like, and united with the inflorescence at their bases; they are followed by two pairs of bractlets (c, d), each of which has a second bractlet (e), on the other hand, remains scale-like, and supports a winter foliage-leaf covered with bud-scales which thins out situated at the base + +A small illustration showing a plant with a long stem and leaves. + +COLUMBIERES. + +of the inflorescence, and is a bud of the 2nd order, in relation to the vegetative shoot. +This bud is always found beneath the inflorescence on the branch placed horizontally, and the winged branches are always found above it, a relation which is observed also in the other genera of this family. The leaves of a branch are antidiomous with regard to each other.—The dichlamydean leaf (Fig. 484), $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $c$ is barren: the two lower bear flowers, or few of $d$, $e$, which soon fall off; $\text{and}$ $\text{the}$ $\text{bud}$ $\text{of}$ $\text{the}$ $\text{2nd}$ $\text{order}$ $\text{is}$ $\text{a}$ $\text{bud}$ $\text{of}$ $\text{the}$ $\text{3rd}$ $\text{order},\,$ in relation to the vegetative shoot. +This bud is always found beneath the inflorescence on the branch placed horizontally, and the winged branches are always found above it, a relation which is observed also in the other genera of this family. The leaves of a branch are antidiomous with regard to each other.—The dichlamydean leaf (Fig. 484), $\text{and}$ $\text{the}$ $\text{bud}$ $\text{of}$ $\text{the}$ $\text{3rd}$ $\text{order}$ $\text{is}$ $\text{a}$ $\text{bud}$ $\text{of}$ $\text{the}$ $\text{3rd}$ $\text{order},\,$ in relation to the vegetative shoot. + +425 + +Figure 484—Diagram of the inflorescence of Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. Tiliaefolia subsp. +
Figure 484—Diagram of the inflorescence of Tiliifolium (Tillea) Linn.
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+ +466 +200COTLEDONES. + +**Family 21: Laguninose.** + +The most characteristic feature is that the gynoeceum is lobular and formed of 1 carpel, the central interior of which is turned posteriorly. The fruit, in most instances, is a legume (legume), which opens generally along both sutures, the two valves twisting more or less in opposite directions. The seeds are usually 1 per pod, but in some cases, as in a psyllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover), or it is indistinguishable as being along one suture only, or as a beryllium (Red Clover),或 + +LEGUMINOSE. +467 + +the same estivation (Figs. 508-510); but in reality there is not a single characteristic which absolutely distinguishes them from the Papilionaceae.—The majority are ascrescent; the leaves as a rule are pinnate or bi-pinnate. The flower is 5-merous, most frequently pterygous and slightly zygomorphic; the calyx is free or united with the corolla, and the petals are often united into a corona. The corona is usually of two kinds: the outer corona is a simple, free, or slightly united, and the inner corona is a double, united, and often very large. The stamens are 10, rarely fewer or more. The fruit is a legume. + +*Crotalaria* (Figs. 508-510) is the largest genus (about 200 species); it has an almost hypogynous, zygomorphic flower with 5 free sepals and petals; of the 10 stamens the 3 posterior are generally barren, the others are of very unequal length and open at the apex by pores (Fig. 509). In some (the *Crotalaria group*) the fruit is + +A diagram showing the structure of a flower. +*Fig. 693.—Floral diagram.* +*Fig. 694.—Flower.* +*Fig. 695.—The stem in long sect.* + +a flat, short, thin, delibating pod; in others (*Catlartarcus*) it is round, long, woody or fleshy, indolent, and divided internally into several parts; in still others (*Crotalaria*) it is a pod. There are seeds.—The following also have dehiscent fruit: *Buniasia* (often lianas, tropical climbers with tendrils [stem-structures] and anomalous stems), *Copajera*, *Hemalotus* (whose pod does not open by pores), *Lobelia*, *Ocimum*, *Papaver*. In *Crotalaria* the corolla resembles that of the Papilionaceae, but the posterior petal is the smallest, and is enveloped by the 2 lateral ones, which are prolonged to form a tube (Fig. 509).—In *Crotalaria* the corolla is *dehiscent* (i.e., the pod is almost round, often a little abstracted between the seeds); the wall is formed by a thin, brittle external layer, enclosing an acid pulp; well-developed + +A diagram showing the structure of a flower. +*Fig. 696.—Floral diagram.* +*Fig. 697.—Flower.* +*Fig. 698.—The stem in long sect.* + +**Crotalaria** (Figs. 508-510).—Crotalaria barbata. +468 + +408 + +**Dicotyledoneae** + +septa are present between the seeds; the most internal layer is parchment-like. Calyx 4-merous by the confluence of 2 sepals. +Only 3 fertile stamens—*Ceratonia siliqua* (Carob-bean, Lucusta)—the pod is long, compressed, with thick sutures, and has a wall, the central one, which is thickened and very sweet; there are transverse septa between the seeds, as in the Tamarind. Embryo greenish in endosperm. The flower is without a corolla, a stigma—*Phragmites* (winged flint), etc.—Kahlebele with *Eucalyptus* (eucalyptus). + +**DISTRIBUTION:** 60 genera, with 760 species; almost exclusively in the Tropics. +The Castor-bean and Cereus grow in the Mediterranean basin. The largest and most widely distributed genus is *Ceris*, which is found as trees, shrubs, and wood in the Mediterranean basin and in Asia Minor. It is a deciduous tree. + +**Morphology:** the leaves and pods of *Ceris siliquosa* and *Ceris unguiculata* (official); Sesame-beans, the fruit-pulp of the *Cerium umbigum*, *Ceridium bicolor*, *Ceridium trilobum*, *Ceridium trilobum* (from a member of Caprifolia-species) (Balm of Gilead) from S. Am. (offi- +cial), and from *Hyacinthus* (Upland balm), Trachysphylus and others. *Edible fruits* are found in the following genera: *Ceris*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*, *Cerium*. The heartwood of several species of Cerisinae, such as C. leucocarpa, C. leucocarpa var. obovata, C. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. obovata, C. obovata var. +**Order 2:** **Papilionaceae**. +The flower (Figs.: 511, 512) is strongly zygomorphic and somewhat perigynous (Fig.: 512 E); most frequently more or less monopetalous. + +**Morphology:** The calyx is persistent and persistent. +The petalary corolla has descending imbricate estivation, +the posterior large leaf, the standard (Fig.: 511 A), and the two lateral ones, the wings (Fig.: 511 B), which again cover the two anterior; these are united in the form of a boat. +The petals of the keel are very asymmetrical. +That the keel is formed of two petals is seen by its position (in front of one sepal) + +Fig.: 511 - Diagram of Faba vulgaris (the bean). The keel covers the wings & the keel. +1 + +LEGUMINOSE. +and by the two stamens more or less free claws. The 10 (5+5) stamens (monadelphous) are either all united into one bundle, or into two bundles (diadelphous), the posterior one being free (Fig. 512 C). The ovaries are curved and also the embryo (Fig. 512 G), especially this hypocotyl, so that the radicle assumes a position oblique to the axis of the fruit, which is thus very short, somewhat wanting; the cotyledons are very rich in protoid reserve material. The forms of the fruit and exceptions are described under the genus. + +A diagram showing a section of a legume flower. +**Fig. 512.—Pisum sativum. A entire flower; B in longitudinal section; C gynoeceum and stamens; D ovary with three carpels; E longitudinal section of ovary; F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X, Y, Z sections of seeds; a radicle; b hypocotyl; c cotyledon; d plumule; e embryo.** +*Genocarpic fruits, i.e., those which penetrate the soil during their development and ripen underground, are found in *Arachis hypogaea* (see page 471), *Phaseolus vulgaris*, *Cicer arietinum*, *Vicia faba*, etc., which grow in various ways. In the majority the cotyledons are raised above the ground as green leaf-like bodies; in the Viciae they remain thick and white, and are eaten as vegetables; in *Cicer* they are thin and yellowish-white, a work of assimilation; in species of *Phaseolus*, on the other hand, they are raised well above the ground and become green, but remain however thin and yellowish. In *Lathyrus odoratus* and *Lathyrus sativus* of the genus are Australian) and *Sorumus* (Sophora, Edwardsii, etc.), represent the oldest + +469 + +470 + +DIOTITLEDONES. +type, as they have to free stemses and so form the transition to the Crucif. +noumies. Nearly all are trees and shrubs. + +3. **Astragalus.** Herbs or shrubs, less frequently trees, with +imparipinnate leaves (without tendrils). The flowers are gener- +ally borne in racemes or spikes. Stamens monadelphous or diadelphous, +the stamens being united by a common base, which is com- +pletely divided longitudinally into 2 loculi by a septum formed by +the incurred dorsal suture. *Dialidophyllum* (Liqui- +roia); *Colutea* (Buddleja) from S. Europe; *Robina* (the false +acacia); by their terminal stipules; *Indigofera* (the Indigo plant); +*Imparfaite* (the false clover), with a single leaf-stalk on each +fruit a nut); *Caryophyllus*, *Witaria* (a climbing shrub), *Galega*. +*Ceratocarpus auricula*, when old, produces flat branches with sole- +like leaves. + +4. **Vicia.** Climbing herba with paripinnate leaves, the midrib ending in a point or frequently in a tendril, which generally is +branched, representing lateral veins without mesophyll; stamens +diadelphous; the cotyledons remain underground on germination. +*Vicia* (Vetches), with a pod of one seed; *Faba* (Bean), with a pod with many seeds; climbing by means of tendrils; the leaves +have many leaflets. *Fabo* (*F. vulgaris*, Horse-bean) is erect, with- +out tendrils; its pod thick with strong septa between the seeds.— +*Struma* (Sorrel), with a pod of two seeds; the leaves are simple +(stylar-brush) on the inner side of the style.—*Pisum* (Pea; Fig. +512) has very large stipules, the best stem has a hollow groove on +the anterior side. *P. sativum* (Common Pea), *P. arvense* (Grey Pea), +*Lathyrus odoratus* (Sweet Pea), with a pod of two seeds, and +most frequently only a few pairs of leaflets. The style is flat- +tened, with ascending hairs on the back. In *L. odoratus* the stipules alone are developed into foliage-leaves, while the remainder of the bud is modified into a bud-scale. The leaves are imparipinnate leaves with dentate or incised leaflets. *C. arviciens* +(Chick-pea)—*Artae* (prestoriae, etc.), the seeds "Crab's eyes"—*Pater- +noster*, *Lathyrus latifolius*.—The flowers are solitary. + +5. **Phasianella.** Herbs, twining or erect, but not climbing by +tendrils; the leaves are imparipinnate, generally ternate, and bear +small, linear bodies resembling stipules at the base of the stalks of the flowers. The flowers are solitary or in cymes; in some cases, +groups of few flowers being situated at short, nodal, lateral axes +borne on a longer stem. On germination the cotyledons are raised a considerable distance above the ground, and become + +LEGUMINOSA. 471 + +greenish, but do not become leaf-like; in P. multifloras they remain underground. Stamens as in the Vetches.—Phasolus (Kidney-bean): the keel with the stamen and style is spirally twisted (to the right). Herbs, twining to this leaf.—The "Calabar-bean" (Phaseolus vulgaris), a climbing herb, with large, white flowers. Spp., Mucuna, Apium, Canavalia, Figna, Dolichos, Cojama, Rhaphiceras, etc. + +6. TRIFOLIUM (Clover). Herbs with ternate leaves; the leaflets are often dentate or crenulate at the base; stamens adnate to the stipules; fruit a legume, 1-few-seeded, pyriform or irregularly dehiscent, or more frequently a nut. The flowers are generally borne in capilla, raceme, or spike—Trifolium (Clover). The corolla is gamopetalous. The calyx persists, together with the corolla, in the fruit. The sepals are free or imbricate; the stipule- or capitulum imbricate; the leaves are ternate, and have adnate stipules.—Medicago (Medick). + +The corolla falls off after flowering; fruit curved like a sickle or spirally twisted; it is a nut, and very numerous seeds are contained in it. The leaves have a small, spherical or lanceolate, thick and wrinkled fruit, which as a rule is indehiscent. The indehiscence is a raceme, often long, or a spike, sometimes a capitulum. Leaves ternate.—Osmun (Redbud); the leaves are compound; the branches are long, in being more shrub-like and bushy, and in having a normal, 2-valved pod, by which characteristic it approaches the Genista. The flowers are generally rose-coloured, solitary, or in few-flowered racemes. The corolla is gamopetalous (3-lobed) and is often present; the leaves are compound with only one small leaflet (the terminal one), or ternate with adnate stipules. + +7. LOTUS. Herbs with ternate or imparipinnate leaves, with entire margins; in P. multifloras the nearest pair of leaf-stalks is placed quite close to the sheath; the stalk of the flower is short and apparently a trifoliate leaf with large stipules is developed. Flowers in an umbel or capitulum. Stamens monadelphous or diadelphous, the filaments (sepals) all alike; only the 5 sepals-stamens are united at their tops.—Lotus (Hind's-finger); it has a long, round pod.—Triptogonodes.—Anystis (Lady's-finger); the fruit is a nut, which is distributed by the wind by means of the membranous bladder-like calyx, which completely encloses and falls off when ripe. + +8. GENISTEA. The majority are shrubs or trees with apparently simple leaves, i.e. compound leaves with only one leaflet (the terminal leaflet), or ternate leaves; the stipules in most instances + +472 + +**dicotyledonae.** + +are very small or are entirely wanting; stamens monadelphous—Guizida (Dyer's weed) has apparently simple leaves; the branches often terminate in a thorn. The strongly-ridged stems in *G. septentrionalis* are its most remarkable characters; the leaves are alternate, simple, entire, and the leaflets are usually rounded to pointed stipules.—*Sarathocnemis* (Broom) has a switch-like, angular branches and often both the apparently simple leaves and the stipules are absent. + +—*Uvifera* (Laburnum). *Ube* (Furze) in *U. europaea*, the serrated leaves have a few foliage leaves, but the leaves ascending these are modified into thorns; *Sparranium* (Celtis), etc., and *Lupinus* (Alpine) is allied to this group; it has a leaf-stipule that is flat, feathery pod, and digitate leaves with minute stipules. + +**9. HENNALEAE** are especially recognised by having the ovary divided by transverse septa into as many cells as there are seeds, and by the style being transversely into nut-like joints (Fig. 53). + +—*Ornithophasis* (Bird's-foot); *Corollus* (Hippocrepia); *Oenothera* (Sainfoin) has a fruit with only 1 seed; *Elaeagnus* (L. Sweden nut); *Elaeagnus* (Egg nut); *Hephaestus* (Hephaestus) and *Aegopogon* (Earth-nut) has a pod which is abstricted between the seeds, and is indehiscent, but is not multi-biocular; the true fruit is a pod which is somewhat wrinkled externally, and ripens underground; the basal part of the ovary is prolonged after flowering, attaining a length of several inches, and buries the young fruit in the soil. The + +For. 60. HENNALEAE. + +known for its medicative properties. + +**10. DALLERACEAE** 25 genera, especially in Tropical America, the majority are trees, shrubs, or herbs; they are used for ornament or for ornamentation. The fruit is rudaceous in all; in some it is a wing, in others a wingless seed (bitchewen, Dallieria); in others it is a pod or capsule (e.g., *Elaeagnus*, *Daphne*, *Elaeagnus*, and *Astragalus*. Some of these genera are the only ones in this family. + +**Follicle**, Especially effected by Bosc. The nectar is secreted by a ring or disc at the base of each flower; the fruit is a dry capsule formed of the receptacle. The flower is constructed with a peculiar mechanism to ensure cross-pollination by insects. The pollen is shed just before the flower opens and adheres to the insect's body; when the insect visits another flower, the flower uses the wings and keel for a landing-stage, and in alighting to reach the honey pressure down the wings and the keel which are locked together near the middle of their length. In this way pollen is brought to the stigma at the upper opening of the keel and a little pollen is thus swept out and deposited upon the abdomen of the visiting insect as it presses against the apex of the keel; + +A diagram showing the structure of a flower in Dalleraceae. + +LEGUMINOSE. 473 + +the insect thus carries away pollen and may effect cross-pollination. In the different flowers this arrangement is modified in various ways to promote pollination. The flowers (Fig. 49) are usually solitary in the Trifolium, where many are inconspicuous forest trees. The following plants belong to the genus *Faba* (*Faba* sativum [W. Asia]; *F. vicia* and *orzerar* [Italy]; *Phasolus vulgaris* [Kulinar- bean, American, French-bean, etc.] and *P. vulgaris var. angustifolius* [Kulinar- bean, the name "angustifolius", F. compressus (French-bean), etc.; *Faboa vulgaris* (Italian, Home-bean, from the Old World); *Erucum laetum* (Lentil, Italian, French-bean, etc.) and *E. sativum* (Lentil, Italian, French-bean, etc.) are popular legumes). The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis subsp. *sativa*, Faba faba, Faba faba subsp. *vulgaris*, *Glycine maxima* (Soybean), *Glycine maxima subsp. *soja*, *Glycine maxima subsp. *soja var. soja*, *Glycine maxima subsp. *soja var. soja var. soja*, *Glycine maxima subsp. *soja var. soja var. soja var. soja*, *Glycine maxima subsp. *soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. soja var. +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis subsp. +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 +473 + +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis subsp. +Glycine maxima (Soybean), Glycine maxima subsp.*soya*, Glycine maxima subsp.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*var.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*var.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*var.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*var.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*var.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*var.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*var.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*var.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*var.*soya*var.*soya*, Glycine maxima subsp.*soya*var.*soya*var.*soya*var.*soya*var.*soy +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis subsp. +Glycine maxima (Soybean), Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* +Glycine maxima subsp.* + +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Faba edulis, Faba faba, Faba faba subspecies of Faba faba, Faba faba +subspecies of Faba faba, Faba faba subspecies of Faba faba, Faba faba subspecies of +Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Faba edulis, Faba faba, Faba faba subspecies of Faba faba, Faba faba +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Faba edulis, Faba faba, Faba faba subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies of Fab +The following are common plants: *Faba vesicaria*, Faba edulis, Faba edulis +subspecies ofFab + +The following are common plants: *Faba vesicaria*,Fabaeedulus,Fabaeedulus subspeciesofFabaeedulus,Fabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafabafa + +The following are common plants: *Faba vesicaria*,Fabaeedulus,Fabeedulus subspeciesofFabaeedulus,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaba,FabefabasubspeciesofFabefaban + +The following are common plants: *FABA VESICARIA*, FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, +SUBSPECIES OF FABAEEDULUS, + +The following are common plants: *FABA VESICARIA*, FABAEEDULUS, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +Subspecies of Fabricaeedulus, + +The following are common plants: *FABA VESICARIA*, FABAEEDULUS + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following are common plants: *FABA VESICARIA* + +The following arecommonplants:F + +**Order 5:** Mimosaaceæ. + +**Flowers** the most frequently hypogynous and regular; the corolla is solente and in the majority of instances that is the calyx also.The flowers generally have two stamens which arise from the base or apex and one which arises from the middle; the latter being frequently wanting.The stamens may be equal or double; they may be free or united; they may be numerous or few; they may be long or short; they may be straight or curved; they may be erect or spreading; they may be sessile or pedunculate; they may be inserted on a receptacle or on a column; they may be inserted on a column or on a receptacle; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be inserted on a receptacle or on a column; they may be insertedonareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronareceptacoleoronarepect + +**Flowers** the most frequently hypogynous and regular; the corolla is solente and in the majority of instances that is the calyx also.The flowers generally have two stamens which arise from the base or apex and one which arises from the middle; the latter being frequently wanting.The stamens may be equal or double; they may be free or united; they may be numerous or few; they may be long or short; they may be straight or curved; they maybe erectorspreadingtheymaybeinsertionoreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptionaloreceptions + +**Flowers** the most frequently hypogynous and regular; the corolla is solente and in the majority of instances that is the calyx also.The flowers generally have two stamens which arise from the base or apex and one which arises from the middle; the latter being frequently wanting.The stamens maybe equalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamensmaybeequalorsinglestamenswhicharisefromthebaseoraapexandonewhicharisesfromthemiddletheslatterbeingfrequentlywantingthestamentsmaybeequalorsinglestamenswhi + +**Flowers** the most frequently hypogynous and regular; the corolla is solente and in the majority of instances that is the calyx also.The flowers generally have two stamens which arise from the base or apex and one which arises from the middle; the latter being frequently wanting.The stamens maybe equalorsinglestamens which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these stamens maybe equalorsinglestamens which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these stamens maybe equalorsinglestamens which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestamens which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestamens which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments which arise from the base ora apex and one which arises from themiddle these latter being frequently wanting these staments maybe equalorsinglestaments whi + +**Flowers** the most frequently hypogynous and regular; the corolla is solente and in the majority of instances that is the calyx also.The flowers generally have two stamens which arise from the base or apex and one which arises from the middle; the latter being frequently wanting.The stamens maybe equalorsinglestamenseach arising frrom either side but not both sides at once but rather alternately with each other in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments in alternate order as shown by their insertion into their filaments + +474 +DOROTYLLADONES. + +frame, but the intermediate portion divides, as in the transversely divided silique, into as many nut-like portions as there are seeds. +Some species have a pod of enormous dimensions. The seeds of *Acacia* *angustissima* (Fig. 513) are very large, and are found on the N. W. coasts of Europe by the Gulf Stream.—The fruit of *Acacia* in some species is an ordinary pod, in others it is transversely divided, or remains an undivided fruit, a nut.—This order includes + +A diagram showing the structure of a pod with multiple seeds. + +FIG. 514.—*Acacia formosana*, a trifoliate-leafed tree. + +both trees and herbaceous plants, which are often thorny; the leaves are usually bipinnate (Fig. 514) and are sensitive, and also possess sleep-movements.—Many Australian *Acacias* have compound leaves only when young, but when old have phyllodes, i.e., leaf-like petioles without blades, placed vertically. A large number have these phyllodes, which in some cases (*Acacia *angustissima*) attain an enormous size, and serve as a home for ants, which in return protect their host-plant against the attacks of other, leaf-cutting ants. + +PASSIFLORINE. +475 + +Other genera besides those mentioned are: *Adenanthus*, *Des- +manthus*, *Parkia*, *Jujuba* (with rather fleshy, indiscernible fruit), *Callianara*, etc. + +1300 species (30 genera); none natives of Europe, their home being the Tropics, and the Old World, especially America and Africa.—Fruits in +Tertiary.—Gums are found in many species of *Acacia*, especially the African +(*Gum arabica*) and Australian, of which some are officinal. The bark, and also the flowers, are used by the natives of Australia as a medicine, and in +tanning ("Babah" is the fruite of several species of *Acacia*). *Cassia* is a +valuable tanning material extracted from the wood of *acacia catechu* (E. Ind.). The genus *Passiflora* is cosmopolitan, with about 200 species, of +fomes. With all they are cultivated as ornamental plants, e.g. *A. spinosa* and +many others, in conservatories. + +The flowers are most frequently regular, 5-memius in the three +most external whorls; usually sessile, solitary or epigynous, less +frequently hypogynous. A characteristic feature is that the + +Passiflora caerulea (Passifloraceae) +ovary is tricarpellary, unilocular, and with 3 parietal placentae which +sometimes meet in the central line (*Oncoceraeceae*). The styles are +generally free and bident. To all these characteristics, however, +there are exceptions. The *Convolvulaceae* are sometimes placed among the +Spermatophyta, but this is not generally admitted. In the *Bignoniaceae*, +from which they differ especially, for instance, in the structure of the ovule. +The position of the Bignoniaceae in this family is also open to doubt. + +476 +DICYOTYLEDONEAE. + +Order 1. Passifloraceae (Passion-flowers). The majority are herbs which climb by means of tendrils (modified branches) and have scattered, stipulate leaves, often palmitiform and lobed (often with a terminal lobe), but in some cases large and beautiful, are regular, $5$, with S5, P5, A5, G3; the calyx and corolla are perigynous, and immediately inside the corolla is the "gynostemium," consisting of two united sepals, two tepals, two petals, or sometimes united in one, and frequently petaloid and the stamens are raised on a long, round internode above the cup-like receptacle; immediately above these is the gynaeceum with its 3 free styles and capitiflora stamens; the ovary is unicellular and contains a placentae. Fruit most frequently a berry. +210 species ; especially in Tropical America. Several Passiflora-species are ornamental plants, and the fruits of some species are edible. + +Order 2. Papayaceae. The best known representative is the Papaya (Carica papaya). A tropical tree, with large leaves usually unlobed or deeply lobed at its summit several large, palmi- +lobed leaves on long stalks. The stem and leaves have latex. The large, Melon-like berries are edible, and for this reason it is culti- +vated in the Tropics. Flowers universal, with slightly different structural characters according to the species. Fruit a berry or a pome. +The $\beta$-flower has a gamopetalous, the $\gamma$-flower a polypetalous corolla. The milky juice contains a substance with similar action to pepine. +10 stamens. 3 carpels. + +Order 3. Turneraeae. 8 species ; specifically in America. + +Order 4. Solanaceae. Nightshade family. + +Order 5. Lamiaceae. Herbaecous plants seldom shrubs, some- +times climbing, and nearly always studded with stiff hairs, in some instances stinging or hooked. The leaves are mostly frequently pubesculated and without stipules. The flowers are regular, $5$, polypetalous or with tepals only; with or without sepals; the me- +nus, or more frequently (by splitting) many stamens, those which are placed before the sepals being generally barren and more or less petaloid; carpels mostly frequency 5, united into an inflorescence of a cyme or panicle; fruit a berry or a pome, +which the receptacle is generally more or less prolonged. Fruit a capsule; in Gomorea an ovary with 1 ovule and fruit a nut. +115 species ; principally from S.Am. A number of annuals are often grown in our gardens : Burseria uva (California) ; Mesembria ; Calophyllum ; Gomonia. + +A page from a botanical book. + +PASSIFLORINE. 477 + +Order 6. *Datisaceae.* 4 species, especially in the Tropics.— +*Datisca cannabina* (Asia Minor) resembles the Hemp in external appearance. The flowers are dioecious, insignificant; ♀-flowers: large, pale yellow, with a few stamens; ♂-flowers: small, with a number of stamens; ♂-flowers: epigynous; ovary unilocular with free, mostly bifid, styles, and generally 3 parietal placentae. In most cases the ovary is not entirely closed at the top (as in *Icedea*). + +Order 7. *Eggoniaceae.* This order principally comprises herbs or subshrubs with scapose stems, having scattered vascular branches in the pith); the leaves are arranged in two rows. + +Fig. 548.—Buprestis ror (reduced). +(a divergence of §) and are asymmetrical, as a rule more or less obliquely cordate, or ovate with cordate base (Fig. 546); large, caducous leaves; the flowers solitary or in a few scattered uni- +pared scrophil cymos; the flowers unisexual; the first ones (the oldest) are ♀-flowers, while ♂-flowers are found especially on the younger axes. The ♀-flowers have most frequently 2+2 colourless petals; the ♂-flowers have 4+4 petals; the head in the centre of the flower; the ♂-flowers are epigynous with 5 coloured perianth-leaves (placed spirally with a divergence of §) and a trilocular ovary, bearing 3 braid styles and 3 wings (the wings usually of unequal size); in the inner angle of each loculus + +478 +**DIOCYTYLEON** + +there is one large projecting placenta, or two plate-like placenta (the bent back edges of the carpels) stalked with ovules. Fruit a capsule, with many extremely small seeds.—*Reynolds.* + +480 species; almost all from the Tropics (Am., Asia).—Many species, with variable flowers, have been described under this genus, but are not representative, chiefly on account of the form, colour, and markings of their leaves; but also for their very beautiful flowers. They reproduce easily by adventitious bulbs from their roots, and are often grown on damp soil; some have bulbils. + +Like the Oxalis they contain an acid sap. + +Order S. *CUCURBITACEAE.* The flower is epigynous, and, as a rule, is also provided with a leaf-like, cup- or bell-shaped receptacle above the ovary, to which the perianth and stamens are attached; the flowers are regular, *axile,* with rudiments of the other sex, and 5-cornate; the corolla is regular and pointed, with the median sepal persistent (Fig. 517), petals usually 5 (rarely 4–5); the corolla is papillosean in the majority, poly-petalous in some; generally pliate-valvate in the bud. *The anthera* + +A B + +Fig. 517.—*Ebullium acris.* Diagram of a & c. & d. flower. + +in the c-flowers are estrope, and monothecous, i.e. only half of each of the anthers of the c-stamen is developed, the pollen-sac having frequently a peculiar *c*-shaped curve (Fig. 518 A, B); the stamens are either all united into a column (as in *Cucurbita*), or they are united at the base of one stamen (as in *Cucumis*); (Fig. 518 A); in the latter case there appears to be one small stamen with a *c*-shaped, curved pollen-sac and two larger ones, each with two curved pollen-sacs placed as in Fig. 517 d. The original form appears to be that shown in Fig. 518 A; sometimes there is a second stamen, sometimes the rudiment of a gymnoceum is present. The carpels are united into an ovary with 3 (4–5) plane-formed by their united edges. These are thick, flabby, and boid, bearing a number of ovoids on each cule (Figs. A17 B; 518 C, D); in general the placenta are + +PASSIFLORINE. 479 + +so large that they not only meet in the centre, but also fill up the ovary as far as the wall of the pericarp. The whole interior of the fruit thus becomes a juicy mass in which three lines may be seen, meeting in the centre (the boundaries of the individual placenta), and making a sort of cross-grain in the fruit. When the carpels are equal in number to the petals they alternate with them. The style is short and thick, and generally divided into 3 (4-5) branches, with a horse-shoe shaped stigma on each branch. + + +A - Cross-section of flower. +B - Longitudinal section of flower. +C - Transverse section of flower. +D - Longitudinal section of ovary. +E - Transverse section of ovary. +F - Shortitudinal section of ovary. +G - Longitudinal section of ovary. +H - Transverse section of ovary. +I - Longitudinal section of ovary. +J - Transverse section of ovary. +K - Longitudinal section of ovary. +L - Transverse section of ovary. +M - Longitudinal section of ovary. +N - Transverse section of ovary. +O - Longitudinal section of ovary. +P - Transverse section of ovary. +Q - Longitudinal section of ovary. +R - Transverse section of ovary. +S - Longitudinal section of ovary. +T - Transverse section of ovary. +U - Longitudinal section of ovary. +V - Transverse section of ovary. +W - Longitudinal section of ovary. +X - Transverse section of ovary. +Y - Longitudinal section of ovary. +Z - Transverse section of ovary. +AA - Longitudinal section of ovary. +BB - Transverse section of ovary. +CC - Longitudinal section of ovary. +DD - Transverse section of ovory. +EE - Longitudinal section of ovary. +FF - Transverse section of ovory. +GG - Longitudinal section of ovary. +HH - Transverse section of ovory. +II - Longitudinal section of ovary. +JJ - Transverse section of ovory. +KK - Longitudinal section of ovary. +LL - Transverse section of ovory. +MM - Longitudinal section of ovary. +NN - Transverse section of ovory. +OO - Longitudinal section of ovary. +PP - Transverse section of ovory. +QQ - Longitudinal section of ovory. +RR - Transverse section of ovory. +SS - Longitudinal section of ovory. +TT - Transverse section of ovory. +UU - Longitudinal section of ovory. +VV - Transverse section of ovory. +WW - Longitudinal section of ovory. +XX - Transverse section of ovory. +YY - Longitudinal section of ovory. +ZZ - Transverse section of ovory. + +Fig. 518—Cucurbita colocynthis. A & D, flower, cut open and spread out; B, stamens; C, flower in long-section; G, receptacle; H, on axis; I, transverse section of ovary. + +(Fig. 518.) The fruit is most frequently a many-seeded berry; in some it attains a considerable size and has a firm external layer (Cucurbita, Lagenaria, etc.). The embryo is straight, has no endosperm, but contains a large quantity of oil. The exceptions to the above rule are the fruits which are fleshy and succulent. + +Exclusively herbs, generally with stiff hairs and yellow flowers. Many species are annuals, others are perennial, having tuberous roots or hypogaeous. The leaves are scattered, long-stalked, in most cases more or less heart-shaped, palmiinerved, palmiplobed, + +14 + +480 + +DIOTYLEDONES. + +and exstipulate; in their axils are found both flowers ( singly, or in an inflorescence) and a vegetative bud, and outside the axil, on the axillary side of the leaf, a simple or branched tendril, by which the plant climbs (exceptions : e.g. Eriolobium). + +The position of the flowers, branches and tendrils situated in and near the leaf-axil is very variable. In some cases the first order of the axis (of the first order), or q, according to the conditions of the various genera. This branch is not situated in the centre of the axis, but is removed slightly towards the axillary side of the leaf. In other cases, however, the first order of the axis, or q, is situated in the centre of the axis, and the anodic side is developed, namely as a tendril, which is displaced to a position outside the axil. The branch of the first order head on its cardiac side has an inflorescence with one or more flowers. The second order of the axis, or q', is a vegetative bud which grows out into a branch like the main axis. The sub-tending leaf of this branch is thus the tendril ; but when it has several arms the compound leaf is then formed. The second order of the axis, or q", unites with its underlying leaf. On this tendril, its leaves also becoming tendrils initiated on an undevolved internode ; the many branched tendril is thus a branch, and its leaves are also branches. The third order of the axis, or q"', is an extending leaf. Other explanations of these difficult relations have been given. + +The protraction of the leaves is due to the fact that a heel-like protraction is formed at the base of the hypocotyl to separate them from each other, and to facilitate the unfolding of the cotyledons. + +Cucurbita (Pumpkin, Marrow) has branched tendrils; the flowers are numerous and are borne singly ; the corolla is bell-shaped, and divided almost as far as the middle. The stamens are all united into a tube; the compressed seeds have a thick, blunt edge. +—Cucumis (Gherkin) generally (unbranched) tendrils; the flowers are borne close together in groups; they are solitary in groups; the corolla is divided nearly as far as the base, and the stamens are united 2–2–1. The connective is elongated above the anthers. The seeds have a sharp angle—Citrullus (Fig. 518) has a corolla similar to Cucumis, but 7 × 2-flowered are borne singly ; the stigma is only 3-lobed; Sphondylium (Squill) has 1 × 1-flowered; Sphondylium (Squiring Cucumber, only 1 species, E. elatiorum) has no tendrils; and is therefore not a climber. The oblong fruit is pendulous from the apex of its stalk, and while ripe is dis tended with an air-cell, which contains water; this water-cell is connected with a tube through which the seeds, together with the watery fluid, are violently ejected through + +If we suppose a spiral line drawn through the leaves separated on a stem with scattered leaves (or in short shoot way), then the side of the leaf just touched in its extatic or descending, and the other, the anodic or ascending side. + +PASSIFLORINE. +481 + +the aperture formed at the base of the fruit. The 3-flowers are borne in racemes near the solitary 3-flowers (fig. 517).—Brugerae (White Hoyo) has chiefly unbranched tendrils and small, greenish-yellow, usually dioecious flowers with rotate corolla, in many-flowered inflorescences; the small, spherical berry has a spore-like appendage on each side. + +The tap-root and a few of the other roots are tuberous. B. alba (berry black; monococcus) and dicoccum (berry red; dicoccum). + +Among the plants which have a tuberous root, the first line a woody external layer which, after the removal of the pulpy integument, may be used as a garl. Luffa has a pectinosey root; the fruit is dry, and consists internally of a number of cells filled with air, which are connected at the summit. Ricciocarpos: the fruit has a leaf, biths coating of wax. Trichosia (Sucka Cucumber) has a thorn, round, long and curved fruit. Monococcum: the flesh is white, and is covered by a thin skin. The fruit is derived from the staminal column which is found in the centre of the 3-flowers, bearing a bi-locular, ring-like rather than opening by a scissor-cleft. The fruit is uni-locular, but is divided into two parts by a thin membrane which incises the seeds. Siegir and Echelus have only unicellular ovaries with one pendulous ovule. The fruit is either a berry or a capsule. The latter is known as the 4-leaf having both halves of the anther. Fimbriae and Tiliacora also have free stamens. Dimorphocarpon has dimorphic flowers. + +In Passifloraceae, as in most of the Solanales, the nectar being secreted by the inner, yellow portion of the receptacle; in the 3-flowers access is gained to the nectar through the slits between the stamens, which arch over the conferring petals and sepals. In this respect they differ from Solanum. Only two are found in the whole of N. Europe: Erioclinum, Erioclinum also and dicoccum; in S. Europe, Echinocactus alone. Most of the cultivated species have been obtained from Asia Minor and Persia. The following are common in cultivation (the "Gourds" mentioned in Scripture are cucurbit chat): from Africa, the Vatia (Cucurbita), from South America, Cucurbita maxima (the Pumpkin), Cucurbita pepo (the Squash), etc. Many species are used in medicine or for domestic purposes. Butter, potted onions are found: the fruits of the tree are used as food: in India, Cucurbita maxima (the Pumpkin), Cucurbita pepo (the Squash), Erioclinum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinum dicoccum (the Gourd), Erioclinium di + +482 + +DIOTYCTOLOXES. + +Family 53. Myrtiflorum. + +The leaves are most frequently opposite, simple, entire (rarely dentate), and exstipulate. The flowers are regular and polygamous (perigynous in Lythraceae and a few others), $\varphi$, polypetalous; the number of members in a whorl is generally 4 or 5 (S, P, A, or most frequently 6 or 7), but rarely 3. It becomes a Myrtaceae when Lycium and Euphorbia are removed to the acridanthae by splitting and the gynoecium also is often different. (When synangium takes place it is principally in the corolla and petal-stamens.) In nearly all instances the calyx is callose. Gynoecium multilocular, multilocular-ovulate, or unilocular-ovulate (except in Lythraceae). The majority of the ovules are situated on axile placentas in the multi- +locular ovary. Endocarpus is vesting in the majority.--Less important sections: Euphorbiaceae and Euphorbiae stipulata. Heterolepidaceae have several stipules. Euphorbiae show no endocarpus. Heterolepidaceae show no endocarpus. + +Order 1. LYTHRACEAE. Hermaeophyte, perigynous flowers which are most frequently 6-merous, viz. S 6 (often with a con- +mensural "epicalyx", Fig. 51 D), one segment posterior, P6, A0 + 6 +or 6 + 0 and G2 - G4, forming a 2-6-loccular ovary; the calyx usually hypogynous, hypogynous style single, and capitula stigmatic. The gynoecium is free at the base of the bollar, or bell-shaped, thalic, strongly veined, with a long style, and a short stigma, leaf-like bud-whorls on its edge and inner side. +Fruit a capsule. No endocarpus.--To this order belong both herbs, shrubs and trees. In the genus *Lycium* (Fig. 51 C) the leaves are opposite, square, the leaves always undulated, entire, and without stipules, or with several very small stipules, and often opposite. The calyx is valvate. The flower is regular (except Cuphea) and frequently large and showy; the petals are generally incised in the bud, and the petala irregularly folded. + +Lythrum (Loose-stripe). The flower is diplotemonous and 6-merous, with a long, tubular receptacle with epicyanoid spicils (Fig. 51 C). The calyx is hypogynous and has ten tiers on the inner side of the receptacle. The gynoecium is bollar-shaped. The flowers are borne in small dichasia in the leafaxils, and their number is increased by lateral branches. The calyx is hypogynous; the leaves are linear-lanceolate to elliptic-lanceolate; the fruit is a capsule. Cross-pollination is chiefly effected by humble- + +MYRTIFOLIE. +483 + +bees and bees, which seek the nectars formed at the bottom of the receptacle. Other species are only dimorphic, or even monomorphic—Closely allied are, Neea, Diphloodenum, Lepidostroma, and Cuphea, whose flowers resemble that of Lythrum; yet is very specific. The calyx is oblique and at the back prolonged into a spur, in which the nectar is secreted by a gland situated between the two sepals col- +lected ; the calyx and corolla gradu- +ally become reduced in size toward +the anterior side of the flower; the +very slender petals are united with +the 11 stamens (the posterior one is +absent); the posterior loculus in the +bilocular ovary is sometimes barren; +but in most cases it is filled with +nectar. The style is long, and at +the posterior side, the ovary as well +as the wall of the receptacle being +ruptured by the placenta, which, +exposed to the air, dries up. The +flowers stand singly in the centre of +the stem, between the pairs of leaves. This +may be seen in the following figure. +Foliage-leaves in each pair, one supports a +foliage-shoot, the other a flower; +the foliage-shoots remain in the axil, +but the flowers are disjoined through the +axils. In this manner, each pair occupies +a position between these two leaves. All foliage-shoots stand in two rows, the +flowering ones in front. + +*Popilia* (Water-purser), a small annual plant, with thin, bell-shaped re- +ceptacle without projecting nectars. The small flowers have no petal-stamens, +and are white or yellowish-white. There are about 50 species (about 12- +565 species; 30 genera; mostly in the Tropics, and more especially S. Am.) +—Some yield dye, e.g., *Lavandula stoechas* cultivated in Africa and Asia) and +*Lavandula officinalis* (Lavender) cultivated—others are ornamental plants, +especially in gardens in warm countries. + +Order 3. *Bryanthaceae*. Tropical Asia and Africa. Tree-like + +**Myrtenaceae** (Myrtle family). A large plant family of the order + +Order 5. *Melastomaceae*. Very numerous and very large order (150 +genera; 700 species). The genus *Melastoma* is very numerous, especially +in Brazil (known by Schumach "The Kingdom of Palms and Melastomaceae"). +There are both herbaceous and herbaceous species, which are easily recog- +nized by their flowers having 5 petals (or rarely 4), and often a few stamens (excep- +tion of a few heather-like species) 3–5–7–9 curved stamens proceeding from the base of the leaf, and connected very regularly by closely parallel, transverse + +Pan. 483—Lythrum salicaria. One of these flowers is shown from all three flowers... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . +pan. 483—lythrum salicaria. one of these flowers is shown from all three flowers... + +454 + +DIOTYLEDONI + +veins. The flower is perigynous or epigynous; its type is that of the Nogaraceae (4-merous; 1 whorl of sepals, petals and carpels, 2 of stamens); the calyx is valvate, the corolla regular, the stamens inserted on the corolla, very characteristic; in the bud they are geniculate, the author opinion in the often long, bent-like, prolonged point, with 1, less frequently with 2 pores, and has generally a short pedicel. The flowers are usually solitary in the capule. These large and beautiful flowering plants play a very important part in South American landscapes; otherwise they are of slight importance (a few are cultivated for ornamentation, e.g., Cordyline, Melianthus, Ledebouria, Echiums, Ricinois, etc.). + +Order 4. **Cenothraceae (or Nogaraceae)**. The flowers are arranged in racemes or spikes, ± epigynous, regular, polytetramers. +*4-merous in all 5 whorls (1 whorl of sepals, petals and carpels, 2 of stamens)*; the calyx valvate or valvate-valvate; the corolla twisted in motivation (the left edge being curved). Gynoecium simple with multicellular ovary; the style is undulated, filiform, and bears a capitulate or -partite stigma; endosperm wanting. +**Cenothaceae** (Nogaraceae) is a monotypic family of herbaceous and marsh-plants; several arborescent. No essential oils. The leaves are alternate or opposite, always single, and without (or with very small) stipules. The odourless flowers sometimes have a coloured calyx. In some species the corolla is valvate-valvate; in others it is valvate beyond the inferior ovary, and finally falls off. The stamens are oblipsomorous (carpel epigynous); the petal-stamens are sometimes suppressed. The anther is sessile or shortly stalked; the pollen-grains are triangular; pollen-grains are connected together by viscous threads. Small stipules are sometimes found, e.g., *Fachia*, *Lepidie*. + +A. Fruit a capsule. (*Bionerae* (Evening Primrose) is 4- merous, thus 8 stamens, a tabular receptacle, and an oblong capsule). + +Fig. 32. – Flower of Lepidie. +with loculicidal dehiscence leaving a centrally placed column, bearing the seeds.—*Eupodium* (Willow-herb) derives from (*Cenothaceae*) especially in the seeds being hairy (at the chalazal end of the seed). +—*Chamaenerion* is a Willow-herb with zygomorphic flowers.—The + +**MYETIFLORE.** 485 + +following may be included here: *Gloriosa*, Eucharidium (an Oenothera with 4 stamens and 3-lobed petals), *Golodia* and *Ricoidendron*. *Jasminum* (dichomeonous sepals), *Jasminella* (petal-stamen absent, sometimes the petal also)... *Lupinus* is peculiar in having the petals and stamens all alike, the former being yellow, the latter white, and the two kinds of flowers on the same plant; the upper flowers are forward and the other backward; the posterior petals are narrower than the anterior ones which are turned obliquely backwards and bent like a knee, with their margins curved upwards, so that they form a kind of hood over the stamens, while the anterior is barren, petiolate, and spoon-shaped; both are sensitive, which is essential for pollination. In Fig. 501, $A$ represents an early stage, in which the stamens are still enclosed by the petals; at $B$, the flower has opened; at $C$, the stamen projects from the centre of the flower; at $D$, the 2 stage, the style occupies the place of the stamens. + +II. Fruit a berry. *Flosca* generally has a coloured calyx and tubular corolla; the corolla may be wanting. + +C. *Fruit a nut.* *Oenocera* (Chenchant's Nightshade) has a 2-merous flower ($S_2$, $P_2$, $A_2+O$ [petal-stamen are wanting], $G_2$). The flowers are borne in racemes without branches... $G_2$. The fruit is a nut-like capsule; it is aquatic plant; the submerged stem has long internodes and lanceolate leaves, falling off at an early period, but at each node are found 4 long roots with thin, internal roots (sometimes erroneously regarded as leaves); the leaves are long and narrow; they float on the surface of the water, bear a rosette of rhombic foliage-leaves, with large, inflated stalks containing air, and forming the floating apparatus of the plants. In the axils of the leaves (as in *Grewia*) S small bulbous bodies are produced; these contain oil-glands and in the axils of the foliage-leaves ($S_4$, $P_4$, $A_4+O$, $G_2$ semi-pygmy-glands. There is an A-blob, cremone situate on the free portion of one leaf; one ovule in each loculus. The fruit is a drupe with 4 or 2 prominent horns (the pericarp is thickened); it is often fleshy. The young berry bears no hooks turning downwards on each side, e.g., reference to similar bundles which formerly lay concealed in the pulp of the sepals. The germination is peculiar: one of the cotyledons is large, and its thick stem runs up through the fruit to reach out into air; another grows out at the apex of the fruit together with the radicle and plumule; the development of the root soon ceases, and the seedling thus grown forth is some entirely submerged bud. This mode of germination described above only takes place when similar shoots arise in the cell of each cotyledon, so that each embryo produces 3–5 shoots... --Tropae... by its mode of life, its fused seeds etc., forms a transition to *Eutropea*. + +The large flowered forms are adapted for insect-pollination and are often regarded as being more primitive than those with smaller flowers themselves. *Eucharis* adapted for hawk-moths and bees--300 species; especially in temperate climates, chiefly in the Northern Hemisphere. *Epilae- + +486 + +**DIOTYLEDONES** + +*Brum*. *Circaea* are natives of this country; *Trapa* is extinct in this country, it has been found in a semi-fossilized condition near Qvinner and in bogs in Den- +mark, and existed in Sweden until a few years ago; *Osmunda* has been intro- +duced from America, and *Lysimachia* from Europe, as ornamental plants in our gardens. The seeds of *Trapa* natans are edible, and used as food in China. + +Order 5. **Holaragicidaceae**. This is a reduced form of the +Euphorbiaceae, and principally differs from these in the presence of +endocarpus and free seeds. Only 1 corolla is each locule—84 species +distributed over the entire globe; the majority are aquatic plants. +The most advanced type is *Hydrophyllum* (Water-Millet), with a +rugulate corolla, and a fruit which is a 2-4-septate schizocarp; +*Hydrocharis* (monocarpus); the fruit is a 2-4-septate schizocarp. +Aquatic plants, most frequently with pectinate, pinnate leaves— + +**Holaragicium** (=a genus specific from the Southern Hemisphere) forms +the next stage, with a corolla which is either pinnate or pinnatifid, with +sepal leaves, with small flowers in crowded inflorescences. The flower, when +fully opened, is a simple corolla, but the sepals are often persistent, +unisexual or with 1 ovule. It is remarkable for the great number of stipules placed in transverse rows in the leaf-base, for the peculiar glandular organs, and for the presence of a large number of stamens in the corolla as a kind of parasite. The simplest form is *Hipparis* (Mar's- +tail) with an extremely small, crenate or entire calyx, without +corolla, and with only one stamen and one carpel, forming an inflorescence, usually a terminal cluster. From it a drupe +with thin pulp. It is a second plant with erect symmetrical leaves, +and erect unshaded shoots, bearing numerous small, verticillate leaves. The small flowers are white. + +Order 6. **Rhizanthaceae**. Tropical trees or shrubs (50 species, the best known being *Bhutia* species, Manguya) which grow vigorously, especi- +ally along rivers and lakes. They have long roots which spread out +broadly, and where they form the so-called Mangrove-swamps. Aerial roots are formed on the stems and branches (Fig. 232 d). The seeds permute in the trunk, and are carried by the wind to distant places; they are +detached from the tree. The radicle projects considerably from the seed, and hangs down freely in the air; when the embryo is finally detached from the other parts of the radicle it becomes an independent plant. The radicle entirely envelops the plumule, becoming detached from the rest of the embryo, which falls down into water. The plumule encloses in its fruit. +The young plant after it has fallen, straws root and grows up through +the undisturbed mud under the trees, or perhaps it may first be drifted about by +the water currents. The young plant then grows up through the intercellular spaces—may also further be remarked that the anther is divided into a number of small loculi. The leaves are stipulate. The endocarp projects from the mesocarp, growing out from the base of the seed, and thus serves as an organ of nutrition to convey nutrient to the embryo from the mother-plant. + +A diagram showing the structure of a mangrove plant. + +MYRTIFOLIE. +487 + +Order 7. Combretaceae. Trees and shrubs, partly linear. An inferior, unilocular ovary with few pendulous ovules. *Conocarpus* and *Lagunaria* form, in conjunction with *Ehretia* tropicale, the tropical *Man- +groves*. The leaves are opposite. + +Order 8. Myrtaceae (Myrtles). The plants belonging to this order are shrubs or trees, the majority being easily recognised by the vegetative characters. The leaves, for instance, are most fre- +quently opposite, without stipules, undivided and entire, pachy- +A +B +Fig. 33.—Ehretia omele with the germinating fruit (much reduced). + +ment-like or leathery, evergreen, aromatic, finely dotted by *petaloid glands containing essential oils*; the venation is penniered with a +nerve just inside and running parallel to the edge of the leaf. +The flowers are regular, usually 5-merous (rarely 4-merous), 5-1, +most frequently 4- or 5-merous in the calyx and corolla, with many +stamens (by splitting, so that they are often in several distinct +bundles) and an ovary with one style, formed of 2–5-many car- +pellets. The fruit is a berry or drupe, sometimes a capsule, smooth +with the ovary. The fruit varies, but is most frequently a berry. +The embryo is thick, often curved with united cotyledons; no +endosperm. + +A small illustration showing a plant with opposite leaves and a long stem. +B A close-up view of the same plant showing the opposite leaves and stem. + +488 +DIOTHELEDOXES. + +1. MYRTEA, MYRTLE GROUP. Chiefly American, though some are found also in Africa and Asia. The fruit is a berry with generally 2-5 loculi in the ovary, and many ovoids in each. --Myrtaea: Eugenia (the pears), Myrica: Jambos; Amomum: Petalidium, etc. +2. PUNICEAE, POMEGRANATE GROUP. Only 2 species (Punica granatum; from India, Afghanistan), differing in several respects from the typical form. The calyx is persistent, 5-lobed, opposite, without glands and marginal veins. The receptacle, onlyx and corolla are red ; the latter 3-5 (generally 6) merous. Calyx valvate and corolla folded as in Lithuncus, stamens also and epipylex as in this order. The most characteristic feature is the inferior, spherical berry, with dry pericarp, formed from two + + +A diagram showing the structure of a berry with two loculi. + + +Fig. 323, 324.--Eugenia caryophylla. +Fig. 325.--Fruit. +Fig. 326.--Long sec. fig. +Fig. 327.--Fruit section. +Fig. 328.--A bud of E. longifolia. +Whorls of carpels in two tiers (Fig. 325): the interior whorl, which is also the lower, has 3 carpels and the placenta are situated in the inner angles of the 3 loculi; the external whorl is 5-merous, and the placenta is situated in the outer angles of the 5 loculi, but their position is changed to the outer side of the loculi owing to the growth of the ovary, which takes place early, causing the carpels to become, as it were, turned inside out; the upper part of the carpel is turned upwards, and the part which was turned inwards becomes turned outwards (as in *Mecombrianthemum*). The edible part of the fruit is the fleshy *kola*, as in *Eibes*. The cotyledons are rolled together spirally. + +6 + +**MYRTIFOLLE.** + +3. LUCITURIDE. The majority are South American. The leaves are scatulated, without petiole glands, and frequently dentate. The flowers are zygomorphic. The woody fruits are globose or oblong or ob-ovoid by a lid. To the genus *Lecythidum* (Lecythus), the seeds will belong to *Lecythis*. + +**Lecythidaceae** (Sapindaceae-mixta from Z. ciliaris, Barringtonia). + +Leucythus is a genus of trees found in South America and the East Asian and Pacific Islands. The fruit is a capsule. The leaves are scatulated, and in some placed adnate by the twisting of the leaf-stalks—Eucalyptus, the Australian Gum-tree, is a well-known example. In the genus *Eucalyptus* the leaves attain gigantic height, e.g., *emodulae* 140-150 m. with a diameter of 8 m. The leaves in *Eucalyptus* are opposite and decurrent on the young plant; on the old plant they are alternate and sessile, simple or pinnate, entire, and lobulate—*Melaleuca*, *Leptospermum*, *Callitris* (the flowers are borne in spikes whose axis continues after flowering, these several forms of fruit may be seen on the same branch). + +Flower opening. + +Figs. 326, 327.—Flowers of *globose*. Fig. 327.—Flower opening. + +4. CHIMELAUCHEAE. Australian shrubs with bush-like appearance; they differ from the other Myrtaceae in having a unilocular ovary with few, basal ovules, and in having a pericarp which is thin and fleshy, but not like many bushes—Chimelaucheae, Doreliaceae, etc. + +This large class (2,100 species) is confined almost entirely to the Troops, being found only in Australia and New Zealand. Of these, only Myrtea seem common—Several are useful on account of the large quantity of volatile oils contained in internal glands—the flower-buds ("Clives" of Eucalyptus coropulata) contain 1% of oil; the leaves of *Myrtea* contain 0.5%, and the fruit-pulp of *Myrtea* contains 1%. The fruit-pulp of *Myrtea* contains 1% of oil; the leaves of *Myrtea* contain 0.5%, and the fruit-pulp of *Myrtea* contains 1%. The fruit-pulp of *Myrtea* contains 1% of oil; the leaves of *Myrtea* contain 0.5%, and the fruit-pulp of *Myrtea* contains 1%. + +Cajuput oil is extracted from the bark of *Cajuputum*, a tree native to Java, and from the wood of *Cajuputum*. (Australia) has had its name been well known on account of its rapid growth, its hard wood, and its amphoteric qualities; it is cultivated on swampy land in Queensland. + +The wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajuputum* is used for making "cigar," and the wood of *Cajupotm + +400 +DIOTYLODIXES. +and fruits of the Bayberry-tree (Fimista arida, W. Im.) ; Guava-cum from the berries of Caracola franciscana. Taxus is found in large quantities c.g. in France, and is also cultivated in England. The genus is very interesting. Ornamental plants cultivated in this country are : Myrtus communis (Mediter- +ranean), several in conservatories, especially the Australian Leptopomera, Eucayptus and others. + +Family 24. Umbelliferae. + +The flower is regular, $q$, and completely epigynous, 5- or 4-merous, with 1 whorl of stamens and 3-5 carpels. Sepals very small, tooth- +like. The corolla is usually regular, frequently with a minute caly- +culus (small petal-like structure) in the Umbelliferae plant. To the rest of the styles, which are generally free, there is an epigynous (undivided, or divided) stelar-leaf ( "styrax-foot", Figs. 528 B, C, D); 530 ; +the number of loculi in the ovary equals that of the carpels ; only 1 product (anther) is produced per loculus. The fruit is a dry indehiscent +spore capsule (capsule). To this must be added that the inflorescence in the majority of cases is an umbel or a capitulum, especially in the Umbelliferae and Araliaceae. Stipules are absent, +but most frequently the base of the petiole forms a large sheath. + +The Umbelliferae are on one side so closely allied to the Rhiinaceae, +especially to the genus Coriaria, that they may be considered as a synonym +continuation of this family. On the other hand, the similarities to the Rhi- +niaceae, especially those between Coriaria and Sambucus, are so great that there is reason to consider them as belonging to the same family. The leaves of the former and the gamopetalous corolla of the latter. Whether this is more than a mere coincidence or whether these two families are related at all +at least should not be inferred in the Rubiaceae, unless it lies in abeyance. The +sepals are very small, as in generally the case in epigynous flowers. + +Order 1. CORNACEAE. The majority of the species are shrubs with solid internodes, opposite (nearly scattered) leaves, which are simple, entire (nearly incised), pinnate-venned, without stipules or large sheaths at their bases; flowers solitary or in cymes; sepals 5 (G), +born in dichasium which are either collected into corollas (e.g. +Corona sanguinea), or in closely crowded umbels or capitula (Corona muscoides), in which latter case there is often a large, +leafy, sterile involucre surrounding the fertile corolla; the base of +the base of the inflorescence; the style is undivided, with lobed stigma; +the ruphs of the ovule is turned outwards. The fruit is a berry or a drupe, +with a 1–4-leukular stone or 2 free stamens. + +Corona (Dog-wood, Cornel) has S4, P4, A4, G2. Leaves opposite, + +1 + +UMBELLIFORE. +401 + +Drupe with a bilocular, 2-seeded stone — *Aucuba*, dioecious ; uni- +bocular ovarian : 1-seeded berry — *Carissa*— *Heliotropus*. +80 species : N. Temp. The fruits of *Coriaria* are edible, the wood is very hard, and the leaves are used in medicine (see *Coriaria* and *Aucuba japonica* Japan) are cultivated as ornamental shrubs. + +Order 2 Ariaceae (*Ives*). Principally trees or shrubs with solid stems. The leaves are scattered, simple or compound, with a sheath at the base, and are usually sessile. They are generally situated in umbels or capitula which are either borne singly or in racemes, or in paniculate inflorescences. The small, most fre- +quently yellowish-green flowers are 5-merous, in the calyx, corolla, +and sometimes in the stamens and pistil. The perianth is often bare, have some other number (2–6). The styles are most frequently several, +free; the capsule of the ovules is turned downwards in the Umbellif- +erous plants. The fruit is a drupe or berry.—Salvia hirta has often +seeds. *Ligusticum* has seeds. *Caryopteris* is a thick plant which is slightly incised, and a distinctly valvate capsule. + +Hedera helix (Ivy) climbs by adventitious roots. The leaves are palmitiform, sessile, and situate on the stemlike branches but often fall off when not lopped on the flower-stalks. The flowers are yellowish-green and open in the autumn; they are slightly prostrate, and are visited by flies and wasps. Burdock: Euphorbia marginata—Pomegranate: *Anisus* with +*Lippia*. + +375 species, 1 genus; especially in the Tropics (R. Asia).—The Ivy, +several species of which are cultivated as ornamental plants. Paper is manufactured from the pith of *Ailanthus paupera* China). + +Order 3 Umbelliferae. The stem is herbaceous with hollow +intertubes; the leaves are scattered, and have a broad, amplexicul +base, a large, most frequently cupulated sheath, and generally a pinnate +(often very much dissected) blade. Entire leaves are found in *Hydro* +ceum erectum. + +The flowers are 5, regular, small, but collected in compound +umbels, that is, in "simple umbels," which again are borne in +umbels (for exceptions see *Hydrophyllum*); the external flowers in +the single umbel being all alike; the internal ones have a common +base as an involucre; the internal ones have no bract; while involucral leaves +are present at the base of the compound umbel, they may be termed +"false bracts." + +The flower has 5 sepals (the median, as usual, posterior), 5 petals, +5 stamens and 2 carpels (in the median line) (Fig. 30). The calyx is often scarcely indicated. The petals have a short claw. + +492 +DICYTODEON. + +are most frequently obcordate, or have an incurved apex (Fig. 528 +B, C), being incised in the bud ; they are white, rarely yellow +(Fennel and Parsnip), blue or red. The flowers are sometimes +symmetrical, but more often asymmetrical, with the petals incurved, +and in that case it is the petal which is directed outside +(anterior) which is the largest, and the two posterior are the +smallest (e.g. Heracleum). The stamens are incured in the bud. +The 2 free styles unite at the base into the "stylus-foet" (stylusoid), +a swollen notory (Fig. 529 B, C); the ovary is bilocular, the niples +of the ovules being directed inward. The fruit is a schizocarp, +dividing into 2 carpels, each of which has 3 sepals which these separate +coincides with that of the union of the carpels, and the two +nut-like mericarps are in most genera kept together for awhile at +the top of a thin, bifid, or undivided stalk (carposporus) which is in +direct continuation with the flower-stalk (Fig. 537). Each mericarp +has more or less 3 ribs on its outer surface, and these are called +the primary ridges (Figs. 530, 532, 534, 535, etc.), of which 3 lie on +the back of the mericarp, the dorsal ridges, and 2 on its edge near +the plane of division, the marginal ridges; five of these (10 ridges + +A-D: Drawings of ovules with flower and fruit. + +E: A drawing of an ovule. + +F: A drawing of a mericarp. + +G: A drawing of a mericarp showing the primary ridges. + +Fig. 528.—Daucus carota with flower and fruit. + +in all in the entire fruit) are placed opposite the calyx-teeth and the others between them. In some genera there are in addition two or more secondary ridges between the primary ones (Fig. 528 E); the secondary ridges are therefore "false ribs". Inside these secondary ridges, when the secondary ridges are absent, all ducts (ventral epidermis) are united with each other, but not necessarily, most fre- quently only one groove; two are also often united on the ventral side of each mericarp. (Figs. 528 E, 530 et al., etc.) The seed is most frequently united with the pericarp. The embryo is small and lies high up in the large, most frequently horny endosperm (Fig. 528 F). The endosperm is usually white, yellowish, or red, and presents three different forms, of important systematic value: (a) those which are quite flat on the ventral side (i.e. the side turned towards the plane of splitting) (Figs. 528 E, 530, 531, 534, 536), (b) those which have a longitudinal groove on the ventral side (Fig. 530), (c) those in which the endosperm on the ventral side is provided with a longitudinal groove, often deep: *Carpylosporella* (e.g. *Anthirius*); the transverse section is nearly a crescent (Fig. 531 Q); (d) those which are convex on the ventral side (hollow in both longitudinal and transverse sections): *Gazozemera* (e.g. *Coronulea*) (Fig. 538). + +The genera are distinguished first of all by the endosperm and forms of fruit, then by the umbel and its structure, i.e. the umbel, the calyx and corolla, by the absciss or presence of an involucre, etc. + +I. *Hydrocotyle*, *Pennywort* Group. Cupulata or simple umbels (all the other groups have compound umbels). No oil-ducts. Orthosepium — *Hydrocotyle* (Penny-wort). The fruits are round to oblong-elliptic (Fig. 529). The calyx-teeth are small. The leaves are peltate—*Didieria*—*Suncinia* (*Suncinia*). The umbels are small, capitulate, gener- ally slightly spreading; they contain 1–4 flowers in the same umbel. The fruits are round, studded with hooked bristles. + +No carpophore.—*Antarcticus* has an umbel sur- rounded by a cupule; this is a very rare feature; with this exception it is the same as the pre- ceding, but the fruit is slightly compressed, with 5 equal ridges. *Hacquetus* (*Dendria*). *Eryngium* (Sea Holly): leaves often thorny. + +**Fig. 529 — Hydrocotyle vulgaris.* Transverse section of fruit.* + +The flowers are all + +434 + +DECTYLOTONDES. + +*scutell*, the inflorescence is thus a capitulum; each flower is often subtended by a bract, which is thorny like the involucre, resembling the *Scutellaria*. The sepals are large. + +*Lecopis*: one of the heads of the every is suppressed. + +2. ANNEIE, Caraway Group (Figs. 530-532). The fruit has only the 10 primary ridges; it is usually short, almost spherical or broadly ovate, and is covered with grooved indumentum. *Carpinus* are + +A. Fruit of Carum carvi; fr. embryo open; x 10 diameters. +B. -Carpinus. Transverse section of fruit. + +most frequently present. Orthospermous (except *Conium*); *Cicutus* (Cow-horn). Polished calyx-leaflets; Glabrous herba with pinnate or bi-pinnate leaves; the flowers in a thick umbel, which is sometimes separated into many compartments; the leaflets are narrow, lanceolate, and dentate; the large involucre is wanting--*Apium* (Celery). No calyx-teeth. *A. graminifolius* (Grass-leaved Caraway). In some species of *Carum*, the umbels are short-stalked or sessile--*Carum* (Caraway). Calyx-teeth small; the large involucre is wanting or is only few-leaved. +*C. carvi* (Caraway). *C. petroselinum*, Parsley (Fig. 530). Fal- +caria: *Anthr*; *Helenium* (Helenium). + +leaves and yellow corolla; *Pimpinella* (Fig. 531); *Sium*: *Rapo- +podium* (*A. podagraria*, Gout- +weed) has bi- or tri-terminate leaves, with ovate, dentate, or crenulate margins; the involucre is wanting--*Conium* is cam- +pylopersernous (Fig. 532); the +fruit is broadly ovate fruit has distinct longitudinal ribs, often +wavy crenulate ridges. *C. +maculatum* (Hemlock) has a round, +smooth stem with purplish spots. + +C. Cucumis melo. Fruit entire and its transverse section. + +UMBELLIFORE. +465 + +3. SCANDICUM. This group has a distinctly oblong or linear fruit which is slightly compressed laterally, and generally prolonged upwards into a "beak"; wings absent. *Campanulaceae*. Otherwise as in the Ammiaceae. *Auriculae* (Beaked Parsley) has a lanceolate fruit, round on the dorsal side, without ridges, but with a ten- +gular beak (Sibthorpius, *Auricula*). *C. umbellatum* (Char- +vil); fruit lanceolate or linear with long, blunt ridges; beak absent or very short. *C. tenuis* has a red-spotted, hairy stem. *Myrrhis* (Cleary); a plant with long and sharp, distinct winged ridges. *M.* +*odora* (Sweet Cleary) has small, yellowish fruits. + +4. SILENEAE. FENNY GROVE (Fig. 533, 534). The fruit is slightly elliptical or oblong in transverse section circular or nearly so, without grooves in the dividing wall; only primary ridges are present. *Orthoporus* (Fennel) has yellow petals; both involucres are wanting; the fruit is oblong. The ridges are thick, all equally developed, or the lateral ridges are slightly larger (Fig. 534).—*Bassia* (*A. cynapium*, *Parsley*) ; the large involucre is very broad, reduced to two leaf-like, small leaves at the base of three linear leaves which run downwards on the outer side of the umbels. The fruit is spherical-ovate, with thick, sharp, keeled ridges, the lateral ones of which are the broadest.—*Dentaria* (Dropwort); the fruit (Fig. 535) has narrow ribs on its sides, with short, blunt ridges and long, erect styles; the ridges are very blunt, the marginal ones a- +triple broader than the others.—*Seuili*, *Lobanotis*, *Ouidismus*, *Siler*, *Silans*, *Meum*, etc. + +W.H. +K K + + +Description: A diagram showing the structure of a flower bud and its parts. +Caption: Fig. 533.—Scandice pholidionis. Fruit entire in transverse section. The ridges at the distal end are unequal. +Caption: Fig. 534.—Fenecium vulgaris. Fruit in transverse section. + + +496 +DICOTYLEDONES. + +5. **Pecunianae**, PASCII GROUP (Figs. 533-537). The fruit is most frequently very strongly compressed dorsally, with broad, mostly winged, lateral ridges. Only primary ridges. The dorsal ridges may project considerably, but are not winged. Ortho- +perma. + +Fig. 533.—Archangelus pectinatus. +Transverse section of fruit. +Fig. 534.—Scordium fitchianum. +Transverse section of fruit. + +a. The winged lateral ridges stand out from each other, so that the fruit appears to be composed of winged (Fig. 535)—Angiospermae; Arch- +angelaceae (Fig. 533)—Lentibulum (Lavergne). + +b. The winged lateral ridges lie close together, and form one wing on each side of the fruit (Fig. 536)—Parnipum (Parnip). + +Cucula yellow. The dorsal ridges are very weak; the oil-ducts do not reach far enough into the fruit to be seen, and small involucres are wanting; leaflets ovate. Anachne (Dill) is a Parnipum with more distinct dorsal ridges and filamentous leaflets. + +**Pecunianae** (Hog-fennel); *Ferula* (with Scordium fitchianum), *Anachne* (Dill); *Cucula* yellow; +—*Hercenium* (Core-parnip); the flowers in the margin of the umbels are often very large, sygomorphous, and projected like rays, e.g., *Hercenium* (Core-parnip); the fruit has very small dorsal ridges; the oil-ducts are more or less club-like and do not reach as far as the base of the fruit (Fig. 537). *Ferula* (with Scordium fitchianum). + +6. **Daucus** Carum Group (Fig. 528). The fruit has 18 ridges, i.e. each fruit has 5 primary and 4 secondary ridges, the latter being often more prominent and projecting further than the primary ones; the oil-ducts are situated under the secondary ridges (Fig. 528). + +a. **Orthophoraceae**: *Daucus* (Carrot). The secondary ridges project much farther than the primary, and bear on their crests a + +Fig. 537.—Scordium fitchianum. +Section of fruit. + +**UMBELLIFORE.** + +407 + +series of hooked spines (Fig. 528 D, E); those are much longer than the small bristles on the primary ridges. The involucral leaves of *D. carota* (Carrot) are numerous and deeply pinate; the inflorescence contracts during the ripening of the fruit, and stane the external umbels hard, but the internal ones remain soft and succulent, and the inflorescence becomes hollow. For the terminal flower, see below. + +C. *Coriandrum sativum*. *Melissa officinalis.* + +b. **Camptosemerium*. *Melissa officinalis.* + +The primary ridges are covered with bristles; the secondary ridges are not very distinct on account of the spines, which entirely fill up the grooves. *Canella* (Barb Parnass). + +c. **Osmorhiza longistylis*. (Coriander) has a smooth, spherical fruit (Fig. 535) with a distinct, 5-dentate calyx, the two anterior (i.e. turned outward) teeth being generally longer than the others; the two fructlets scarcely separate from each other. + + +A B C D E + + +Fig. 538. --*Coriandrum sativum*. b secondary ridges; c primary ridges; f endosperm; i embryo. + +naturally; all the ridges project only very slightly, the curved primary ones least, the secondary ridges most. + +**Pollination.** The flowers are adapted for insect-pollination; they execute no such as in *Cnicus benedictus*, but rather small and insignificant, but yet are rendered conspicuous by being always crowded in many-flowered inflorescences. *Primula* is common, sometimes to such an extent that it is almost a monotypic genus; but in this case also the primary ridges (Fig. 539, Z). Insect visitors are more frequent and numerous as in the inflorescences of *Coriandrum*. The number of secondary ridges per flower characterised intergrading among the others (Fig. 539), and the number of these becomes greater on the umbels developed at the latest period. A terminal flower is often found in which one or two secondary ridges are in colour alone (purple), is sometimes found in the umbel. The nectar lies so exposed and flat that the flowers are principally visited by insects with short proboscides, such as bees and flies; ants are rarely found, and beetles rare.--1400 species (150 genera); especially from temperate climates in Europe, Asia, N. Am. About 60 species in this country. + +498 +DIOTYLEDONAE. + +Urea. A few are cultivated as ornamental plants. They are, however, useful in medicine, and for culinary purposes on account of the essential oils and provitamins contained in them. The following species are of the genus Urea: -- Urea (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) (Urea) + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 + +498 +A small image of a plant with green leaves and a yellow flower. +--- E. Mediterraneum); Coriandrum sativum f. Coriander; S. Eur.; Genista +phlebodesum; Water Drop-urut; Cuminum cyminum; Pimpinella anisum; Africn; +cultivated in Egypt and Syria; and the following are used as pot-pourris: Anthyllis +corydalis; Aethusa cynapium; Myrrhis odorata +(Sweet Mint); Orontis; Chamaemelum nobile f. [the great parsley]; Hamamelis; +Hamamelis virginiana; Lysimachia vulgaris; Satureja hortensis; Satureja +Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis; Satureja +hortensis; Satureja hortensis; Satureja hortensis; Satureja hortensis + +--- E. Mediterraneum); Coriandrum sativum f. Coriander, E. Eur.; Genista +phlebodesum, Water Drop-urut, Cuminum cyminum, Pimpinella anisum, Africn, +cultivated in Egypt and Syria, and the following are used as pot-pourris: Anthyllis +corydalis, Aethusa cynapium, Myrrhis odorata +(Sweet Mint), Orontis, Chamaemelum nobile f. [the great parsley], Hamamelis, +Hamamelis virginiana, Lysimachia vulgaris, and the following are used as pot-pourris: +Anthyllis corydalis, Aethusa cynapium, Myrrhis odorata +(Sweet Mint), Orontis, Chamaemelum nobile f. [the great parsley], Hamamelis, +Hamamelis virginiana, Lysimachia vulgaris + +--- E. Mediterraneum); Coriandrum sativum f. Coriander, E. Eur.; Genista +phlebodesum, Water Drop-urut, Cuminum cyminum, Pimpinella anisum, Africn, +cultivated in Egypt and Syria, and the following are used as pot-pourris: Anthyllis +corydalis, Aethusa cynapium, Myrrhis odorata +(Sweet Mint), Orontis, Chamaemelum nobile f. [the great parsley], Hamamelis, +Hamamelis virginiana, Lysimachia vulgaris + +--- E. Mediterraneum); Coriandrum sativum f. Coriander, E. Eur.; Genista +phlebodesum, Water Drop-urut, Cuminum cyminum, Pimpinella anisum, Africn, +cultivated in Egypt and Syria, and the following are used as pot-pourris: Anthyllis +corydalis, Aethusa cynapium, Myrrhis odorata +(Sweet Mint), Orontis, Chamaemelum nobile f. [the great parsley], Hamamelis, +Hamamelis virginiana, Lysimachia vulgaris + +--- E. Mediterraneum); Coriandrum sativum f. Coriander, E. Eur.; Genista +phlebodesum, Water Drop-urut, Cuminum cyminum, Pimpinella anisum, Africn, +cultivated in Egypt and Syria, and the following are used as pot-pourris: Anthyllis +corydalis, Aethusa cynapium, Myrrhis odorata +(Sweet Mint), Orontis, Chamaemelum nobile f. [the great parsley], Hamamelis, +Hamamelis virginiana, Lysimachia vulgaris + +--- E. Mediterraneum); Coriandrum sativum f. Coriander, E. Eur.; Genista +phlebodesum, Water Drop-urut, Cuminum cyminum, Pimpinella anisum, Africn, +cultivated in Egypt and Syria, and the following are used as pot-pourris: Anthyllis +corydalis, Aethusa cynapium, Myrrhis odorata +(Sweet Mint), Orontis, Chamaemelum nobile f. [the great parsley], Hamamelis, +Hamamelis virginiana, Lysimachia vulgaris + +--- E. Mediterraneum); Coriandrum sativum f. Coriander, E. Eur.; Genista +phlebodesum, Water Drop-urut, Cuminum cyminum, Pimpinella anisum, Africn, +cultivated in Egypt and Syria, and the following are used as pot-pourris: Anthyllis +corydalis, Aethusa cynapium, Myrrhis odorata +(Sweet Mint), Orontis, Chamaemelum nobile f. [the great parsley], Hamamelis, +Hamamelis virginiana, Lysimachia vulgaris + +--- E. Mediterraneum); Coriandrum sativum f. Coriander, E. Eur.; Genista +phlebodesum, Water Drop-urut, Cuminum cyminum, Pimpinella anisum, Africn, +cultivated in Egypt and Syria, and the following are used as pot-pourris: Anthyllis +corydalis, Aethusa cynapium, Myrrhis odorata +(Sweet Mint), Orontis, Chamaemelum nobile f. [the great parsley], Hamamelis, +Hamamelis virginiana, Lysimachia vulgaris + +--- E. Mediterraneum); Coriandrum sativum f. Coriander, E. Eur.; Genista +phlebodesum, Water Drop-urut, Cuminum cyminum, Pimpinella anisum, Africn, +cultivated in Egypt and Syria, and the following are used as pot-pourris: Anthyllis +corydalis, Aethusa cynapium, Myrrhis odorata +(Sweet Mint), Orontis, Chamaemelum nobile f. [the great parsley], Hamamelis, +Hamamelis virginiana, Lysimachia vulgaris + +--- E. Mediterraneum); Coriandrum sativum f. Coriander, + +This family includes only parasitic plants. +Partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. +Again it is a matter of doubt 1 those marked + are official and when no home is stated the plant is na- +1 Those marked + are official and when no home is stated the plant is na- +ative. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +native. +-native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated the plant is native. + +Family 25. Hysterophytaceae. + +This family includes only parasitic plants partly on this ground partly because they all have epigynous flowers they are considered to belong to the youngest group of families in the order but that one that comes after it is not certain to which of the preceding families they are most nearly allied. + +Again it is a matter of doubt those marked + are official and when no home is stated + +HYSTEROPHYLLA. +409 + +whether the Aristolochiaceae are related to the olibera; they are by Engler united with Buteaceae into one family, *Aristolochiales*. + +Order I. *Aristolochiaceae*. The majority are perennial herbs or twining shrubs, whose stalked, simple, and generally more or less compound, pinnate leaves are borne in 2 rows and are ex- +stipulate. The flowers are regular, usually 5-parted, hypogynous or zygomorphic; perianth-bases united, simple but most frequently petiolate and 3-merous; 6 or 12 (in *Thottea* as many as 36) stamens with exserte anthers. The corolla is more or less tubular, 5-lobed, 5-lobular with crurae attached in the inner angles of the loculi (Fig. 540 b). The style is short, straight, or a little curved; stigma (Fig. 540 c). Fruit a capsule. Seeds rich in endo- +spores. + +*Asarum europaeum*. Each shoot has 2 reniform foliage-leaves, between which the ter- +minal flower is borne (the rhizome produces a pseudorhizome by development of the bud in the axil of the upper foliage- +leaf). The flower is regular and has 6 broad petals, with 3 outer valvate, and 3 +inner small segments (which may be wanting). $12$ (2+6) +free, erect, opposite each other. + +*Aristolochia clematitis* (Birthwort) has an erect, unbranched stem, bearing many flowers in the lower part of the leafy shoots (accessory buds in a uniseriate scorioid cyme). The flowers are zygomorphic (Fig. 540), formed of a tube (part $1$) and 3 free, +cus whorls. The perianth has a lower, much-distended part ($2$), succeeded by a narrow, bent +tube ($3$), which passes over into an oblique, almost tongue-like pro- + +Fig. 541.—Flower of *Aristolochia clematitis* (Birthwort). A Before pollination, and B after pollination. $1$ Lower part of corolla; $2$, $3$ corona. + +A diagram showing the structure of a flower of *Aristolochia clematitis*, including parts $1$, $2$, and $3$. Part $1$ shows the lower part of the corolla. Parts $2$ and $3$ show the corona. + +500 + +DUCOTYLLERACEAE. + +jection (6 vascular bundles indicate that the number 6 is prevalent here, as in *Aurinea*); 6 stamens (Fig. 540 a), with the dorsal-portion turned upwards, are united with the short style to form a single column, which is inserted at the base of the ovary, and has two stigmatic rays, which arch over them as short, thick lobes; Protoporangium is effaced in *Auricula* clematis by small flies; these enter the tube of the flower, and, after having been prevented by the stiff, downwards-turned hairs which line the tube and prevent their escape; they find the stigma (a) fully developed, and may pollinate it with pollen from other flowers. The petals are white, and wither ($P_1$), the anthers open, and the filaments may again be covered with pollen; but the hairs which blocked up the tube do not wither until the anthers have been shed. The stamens are then removed from the scape and effect cross-pollination. Prior to pollination, the flowers stand erect, but after this has taken place they become pendulous, and the perianth soon wilts. The flowers are produced in racemes on long stems, and grow in gardens; it has only one row of accessory buds in the leaf-fascicles—300 species; chiefly in S. Am.; ORNAMENTAL: the rhinoceros of *Arctolochia argentea* (N. Am.). + +Order 2. Santalaceae. Parasites containing chlophyll, which, by the help of peculiar glands, can live without chlorophyll; they are found in the roots of other plants. Some are herbs, others under-shrubs. The regular, most frequently 3-flowered with a simple perianth, which is gamopetalous, 3-or 5-partite with a central column of stamens opposite the petal-leaves. In the inferior ovary there is a free, centrally placed, often long and curved placentas with three cavities (one opposite each carpellary); these are naked, or in any case infertile integuments. Fruit: a nut or drupe. Seed: 1 or more seeds. Seedling: a herb with alternate leaves; rarely a tree native, a herb with subterete, linear leaves and a short stem (Fig. 541 b). *Santalum album* (55, G3) in erect racemes; the subtending bracts are linear-lanceolate; fruit: nut—*Oryzae* (Glutinous shrub); 5-membranous perianth—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemes; fruit: nut—*Santalinum alatum* (55, G3) in erect racemos +Fig. 141—a frut of *Xanthosoma houtteanum*, showing mag. 2 mm., growing on a branch. +end., yields the valuable, +scented Sandal-wood, the +leaf of which is used medi- +cinally.—Quassimomium. + +1 + +HYSTEROPHYTA. +501 + +Myrcodendron is a reduced form of the Santalaceae; the $d$-flowers are without perianth; the pericarp of the $Z$-flower is 3-merous. About 7 species; S. Amt.; parasitic on trees, and having a root-like caudex. The fruit is erect, terminat- +ing with the lobes of the calyx, which serve as flying organs and to attach the fruits to a branch (Fig. 541), the branches twining round as soon as they come in contact with them. The seeds are minute, and are contained in a hard, negatively helictotax hypogynous, and is attached by a radicle modified into an haustorium. + +Order 3. Loranthaceae (Mistletoes). Plants containing chlorophyll which are parasites on trees, and most frequently have, in addition to the flowers, leaves of various kinds, regular, epigynous, often unisexual, 2- or 3-merous flowers, with single or double perianth. Stamens equal in number and opposite to the perianth-leaves, free, or in varying degrees united to one another. The inflorescence consists of a few or many racemes or panicles bearing situated on a low, free, centrally-placed placenta, but the placenta and ovules unite with the wall of the ovary into connected, paren- +chymatous masses, in which the embryo-sac is enclosed. Only 1 +(less than 1%) of these plants are parasitic on trees. The num- +ber of the carpels however varies. The fruit is a 1-celled berry, +whose inner layer is changed into a tough allose mass (third-lime), +which serves to attach the fruits to other plants. + +The two groups, Loranthodes and Flicinaceae, are distinguished by the fact that the latter group has no true flowers, either regular or lobed, or dentate swelling on the receptacle below the perianth. The majority of the Loran- +thodes have a petiolate perianth; in all the Viscaceae, on the other hand, it is sepalate. + +The Mistletoe (Viscum album, Fig. 542) is a native, evergreen +plant which may be found growing on almost any of our trees +(sometimes on the Oak), and, like other Loranthaceae, it produces swellings of the affected branches. Its sperical white berries (Fig. +543) are produced at the ends of short lateral branches (especially +Tussilago), and are partly seen with their extremity, partly spread or bent back off the branches of the tree; the seed being enclosed, at maturity, by thorns, i.e., +"thorns," which are formed from the outermost scales of the perianth first passed through the alimentary canal of the bird. On germination, the hypo- +cotyl-first appears, as in Fig. 541, and becomes a short stem; then the apex of this stem grows downwards into a disc-like haustorium, from the centre of which a root-like body grows through the base into the wood, and thus attaches itself to some other tree. The roots grow out like +strands which are formed in this manner; however, without having a root-cap; +they are green, and penetrate the wood by the medullary rays (Fig. 544 C). +Adventitious buds may also be developed from the root-like strands which break + +502 + +DIOOTTLEDONER. + + +A sketch of a plant with small leaves and a single flower. + + +Wat. All.—Flower allium ; A branch with leaves and berries ; a scale-leaves ; 1 foliag- +leaves ; n = n flowers ; B seedling, the bark of the branch being removed ; O an old +embryo which still remains the cotyledon. + + +HYSTEROPHYLLA. +503 + +through the bark and emerge as young plants. The young stem quickly assumes its longitudinal growth, and lateral shoots are developed from the axils of its foliage-leaves. These and all following shoots have a similar structure, each of them bears a pair of scale-leaves (Fig. 388, a, b) and a pair of foliage-leaves (Fig. + +Fig. 388.—To the left the Baffioniscus Cyaneus agnostus, parasitic on the roots of Glo- +al. To the right: the Baffioniscus Coniurus constrictus, parasitic on the roots of +Saliornis. +s. To the right: the Baffioniscus Coniurus constrictus, parasitic on the roots of Saliornis. + +504 +DICOTYLEDONI + +342. 4, 6), and then terminates its growth, if it does not produce an inflorescence; new lateral shoots proceed from the axils of the foliose leaves, and the branchlets, in some cases, are also produced by the nodes of the stem itself. The flowers are intermedio (short-stemmed) formation is formed each year, so that each fork indicates one year. The foliose leaves fall off in the second year. The inflorescence is a 3-5(-7) flowered panicle, with a few sterile branches. The flowers are perfect, and open with a pow; this relationship may be considered to have arisen from the union of the perianth-leaves with the multilocular stamens (3-2) phalous operation. The flowers are perfect, and open with a pow; this relationship may be considered to have arisen from the union of the perianth-leaves with the multilocular stamens (3-2) phalous operation. Thus, it is also found in Europe (it has a 5-nerved flower), especially in the central and southern districts, on *Quercus cerris* and *Quercus petraea*; but the great majority of the species are found in Asia, where they are ornamented with their often brightly-coloured flowers, and ultimately kill when pressed in ten great numbers. The pollination in the numerous Loniceraeum with numerous flowers is effected by insects, which visit them during the active period in autumn, the actual fertilisation in the following spring, and the majority in November. In those of the succeeding month of May they bear a real perianth, and fall off. + +Uses. **Bilberry** from *Cerium alba*. + +Order 4. *Rafflesiaceae* and Order 5. *Balanophoraceae.* These orders con- +sist two families, which are very distinct from each other; they are reddish or yellow without foliose-leaves (Fig. 548). As far as our knowledge of these rare tropical plants extends, they have thalloid organs of vegetative reproduction through their stems, either as rhizomes or tubers (Fig. 549); or as fleshy roots (Fig. +hypophytes); they live in and on the tissues of the host-plant, from which their flowering-shoots, often of mushroom-like form, are subsequently developed (Fig. 548). In order to induce them to grow through the tissues of the host-plant. + +Of the Rafflesiaceae, *Cytinus hypocistis* is found in E. Europe living on roots of *Cotoneaster* (Fig. 549). Of the Balanophoraceae, *Balanophora*, which is the best known tree; it lives on roots of *Cerium-species belonging to the Amur- +leaves*) in Asia; its yellowed root, yielding flowers at a gigantic size (one metre or more), is used as a medicine; it is also employed as food by the host-plant. Besides these there are other genera: *Brassicaea*, *Pittosporum*, *Hydrangea*. To Balanophora (Fig. 549) belong *Euphorbia*, *Lepidodendron*, *Spathodea*, *Hesperis*, *Helianthus*, etc., and in Eur. Eur. *Cyamopsis tetragonolobus.* + +Sub-Class 2. Sympetalae + +The characters which separate this from the first Sub-class, the Chiripuntiatae, have been described under p. 336. They consist in +the following: the flower is always verticillate, generally with 5 +sepals, 5 petals, 5 stamens, and 2 carpels (in the median plane), +the calyx is generally persistent and gamopetalous, the corolla is +gamopetalous and united to the stamens, which are therefore + +SYMPETALAE. + +505 + +admit to it, the ovules have only one thick integument and a small nucellus. (The exceptions are noted later.) + +This Sub-class is no doubt more recent than the Chortopetalæ; it is also peculiar in including fewer trees and shrubs than the latter. + +The Sympetaleæ may be separated into 2 sections— + +A. The Sympetaleæ which have 3 petals in this section have 5 whorls equal in number, namely, 2 terminal whorls in addition to the calyx, corolla, and carpel; in some instances, one of the staminal whorls is rudimentary or entirely suppressed, but in this case the petals are placed opposite each other, as in the preceding order, and the whorl which presents stands opposite the petals. The flowers are regular. The number of carpels equals that of the sepals, but in one of the orders (Dicoccos) they are opposite the petals, and in another (Corynose) they are opposite two orders (Primuline and Diapogonæ) they are placed opposite the sepals (the flower being ditheplostemonous). This section is the most closely allied to the Chortopetaleæ, since the petals may sometimes be reduced to one or two, and the carpel is always found on the receptacle (Eriocentra); or ovules with two integuments are also found. It is very doubtful whether the orders included under this head have any relationship with the other Sympetaleæ. They appear to any case to represent either + +B. Tetracyclice (four-whorled). The flowers have only 4 whorls, namely, besides sepals, petals, and carpels, only one whorl of stamens. In this order there are 4 terminal whorls of petals of the second staminal whorl, and when the number of carpels is the same as that of the preceding whorls ("isomorous") they alternate with the stamens; but in most cases there are 3 carpels placed in the median plane (as in Dicoccos), or there are 2 carpels (as in Corynose), or there are none at all (as in Eriocentra). + +This section is the largest, and the one which shows the characteristics of the Sympetaleæ best. Very irregular flowers are met with. + +The following families belong to the Tetracyclice: 26, Dicoccos; 27, Diapogonæ; 28, Corynose; 29, Eriocentra. + +The following families belonging to the Tetracyclice are— + +a. **Hygrothecae** (flowers with few integuments): 29, Tetraclem; 30, Porionae; 31, Nuciferae; 32, Contortae. + +b. **Erythrococcaceae** (flowers with many integuments): 33, Canescentia; 34, Erythrococcus. + +The ovules and ovaries in the last family are always reduced to one; and at the same time the fruits become nuts, and the flowers are united into crowded inflorescences. + +506 +DIOCTYLEDONAE. +**A. Pentacyclium.** +Family 29. Bicornes. + +This family is chiefly composed of shrubs, less frequently of small trees, or perennial herbs; their leaves are undivided, most frequently evergreen, stiff and leathery, and always without stipules. The flowers are 5- and regularly rarely slightly zygomorphic, most frequently regular, and 4- or 5-merous through all the whorls. The stamens are attached to the corolla-tube, a rule which is quite free from the petals, an attachment which is very rare among the Gamopetalae. They have a simple gynoeceum with one undivided style, a commissural stigma, and a multilocular ovary, whose cells are usually united into tetrad (Fig. 542 D), but have a large number of ovules. The placentae are sometimes united not only, and in consequence, the ovary is Lobular with incomplete partition-walls, e.g. *Pyrula*, *Manettia*, etc., straight, with endosperm. The corolla is very delicate, approximate the petiole. + +The diagram is generally Sa, Pa, n+1n, gn, in which n is 4 or 5. To this may be added, that the corolla is in most cases gamo- +petalous, but occasionally (especially *Pyrolaceae*) perfectly polypetalous; and that the inflorescence is often compound, with some +like appendages (hence the name "Bicornes" (Figs. 543, 546); frequently the two halves of the anther are also widely separated from each other at the upper end, so that the pores are placed each one at the base of an anther (Fig. 542 A). In many plants the majority are united into tetrad (Fig. 542 D)—The flowers, as a rule, are pendulous and borne in racemes, coloured (red or white), but odourless. When the fruit is a capsule, the placentae occur on many of its sides. + +The majority of plants belonging to this family inhabit cold and temperate countries, or high mountains in tropical regions; they prefer dry or damp places (hogs, heaths, etc.). Plentiful in N. America. + +Order I. Pyrolaceae. Perennial herbs; petala usually frequenty quite free from each other, and falling off singly after flowering; the antarrials are opposite or subopposite (Fig. 543 A), or by a transverse vein. The placentae are thick. The seeds in the capsule-like fruit (loculicidal dehiscence) are exceedingly small and light; they have a sac-like testa which loosely envelops them, an only encephalum, and an extremely simple embryo, which consists + +**BIGNONIACEAE.** + +only of an ellipsoidal, cellular mass, without cotyledons or differen- +tiation into plumule and radicle. + +*Pyrola* (Winter-green) is green, and has also large evergreen +foliage-leaves. The flowers, 5-merous, are most frequently borne +in racemes without a +terminal flower. +The +anthers are extrorse +in the bud with the +pore-like stigma in posi- +tion (Fig. 544 A), but +they become inverted at a later period, so that the +stigma is at the top (Fig. 544 C). + +*P. trifolia* has a single, +terminal flower; *P. winteri* +is sterile. + +From these in the spring aerial, quite unshaded shoots. *Chrysosplenium alternifolium.* + +*Montiastrum* (Yellow Bird's-nest) is very pale yellow, without +champagne scent, and has a long, slender stem, which is covered +upon the stem; it is a saprophyte. The raceme has a terminal +flower, and is pendulous before flowering. The anthers open by a +semicircular, transverse clef. *M. hypogaeum* reproduces chiefly by root- +shoots. + +About 30 species, especially N. Europe, N. America, and E. Asia. + +Order 2. **ERICACEAE.** The flower (Fig. 545) is hypogeous, the +median sepal posteriorly prolonged to form a cupule; the sepals are +generalised and the fruit is a capsule, frequently a berry or drupe. +At the base of the ovary is a nectar-secreting disc (Fig. 545 B). This order comprises shrubs or undershrubs +(nearly small trees), which are evergreen, and as a rule have densely pubescent leaves. + +1. **Ericaceae**, Heath Group. Flowers most frequently 4-merous +(8A, 4A + 4, GA, united in a 4-localar gymnoecium), rarely 5- +merous. The withered corolla persists after flowering. The leaves are mostly simple and entire; some are pinnate; all have basal lobules without scales. The fruit is a capsule—*Cultus* (G. vulgaris, Ling) has a deeply-lobed corolla, which is less than the coloured +sepals; *E. tetralobum*, Cross-leaved Heath has a tubular or bell- +shaped, 4-lobed corolla, which is much longer than the calyx. +Capsule with loculicidal dehiscence.—*Pentapodaceae.* + +A small illustration showing parts of a plant. +507 + +508 +DICOTYLEDONES. + +2. ANDROIDEAE. The flowers are 3-merous (S5, P5, A5+5, G5), with decussate corolla. Capsule with localised dehiscence. The leaves are serrated, and incline more to the ordinary broad-leaved form.---Andromeda; Gaultheria; Cassiopea; Euphrasia; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Cassiopea; Fig. 546.—Arctostaphylos uva-ursi. + +3. ARCTEEAE. The flowers are in the preceding group (Fig. 545), but the fruit is a berry or drupe. *Arctostaphylos* (A. uva-ursi, Bearberry) has a spherical berry; *Arbutus* (A. unedo, Strawberry-tree) has a fleshy, fleshy-pulpy, in other species there is 1 stone with several loculi. *Arbutus* (A. unedo, Strawberry-tree) has a spherical berry. + +Pollination is effected by means of insects, especially by bees. The pollen is light and dry, and is shaken out through the pores of the anthers when the insects nectarize on the flower. In some cases the flowers are solitary, and take place, no doubt, in many cases—300 species; the very large genus, *Erico*, especially in S. Africa (the Cape)—Ovularia: the leaves of *Drepanis* are linear; *Corydalis* has a tuberous root; *Eriocaulon* has a tuberous (otter-wire-like) fruit. Many Erico-species are cultivated as ornamental plants. + +Order 3. Rhodoreaceae (Rhododendron). This differs from the preceding order in the median sepal being anterior, and hence the position of the other floral whorls is also reversed. The flower is hypogynous, and sessile on a short pedicel; the sepals are fre- +quently deeply cleft or peltate, and falls off after flowering; the authors open by pores, and have no horn-like appendages. Capsule with apical dehiscence.—The shrubs or small trees belonging to this order are mostly evergreen; they have large leaves, and the buds are generally provided with large leaf-buds. +Rhododendron has 10 stamens, and a slightly zygomorphic flower with deeply 3-leaf corolla (the section *Azalea* has frequently + +14 + +**BIGNONIACEAE.** + +only 5 stamens, the petal-stamens being absent). They are Alpine plants (200 species) in the mountains of Asia, especially the Himalayas ; some in S. Europe. —*Mentzelia*. *Lodum*. small, rusty-brown, hairy shrubs with polypetalous, expanded, star-like corolla. +—*Kalisun* (*N. Am.*) has a cupular corolla, with 10 small, pocket-like lobes, and a long tube. The petals are small, and the arched, elastic filaments are freed from this position by means of the insects, when they quickly straighten themselves in the centre of the flower. —*Phyllodiscus*. *Louviensis* (5 stamens); (*Clethra*) (?). + +About 370 species. Several species are ornamental plants. Several plants of the order are more or less nutritious. *Lodum palustris* has been used as a sub-stitute for hops. + +Order 4. Diapensiaceae. Hypogynous flower. 8 staminae beneath the corolla. 45–65. —The corolla is usually of the cucullate-Funnel-shaped genus. Disc absent. Capsule cupuliform.—Some species from the Arctic regions. It is doubtful whether this order should be included in the Berberidaceae or in the Ericaceae, or in a separate family. + +Order 5. Ericaceae. —This order comprises those species of the family which are confined to Australia and the South Sea Islands. They are shrub-like plants, with opposite leaves, and with a corolla of 4–5 petals, often with the structure, form, and colour of the flower. They differ specially in having no disc, and in having only 4 stamens (or 5), and in having no fruit, having only 1 locule, and opening by a longitudinal slit. Fruit must frequently be drupe (or loculicidal capsule). *Ericaceae* and *Sphagnaceae* species are ornamental plants. + +Order 6. Vacciniaceae (Bilberries). The flower (Fig. 546) is bilobed; the calyx is generally cupular, and the corolla is bilobed. The latter is most frequently symmetrical, and bears on its apex the calyx, which is generally very low, almost entire, and with a disc-like expansion inside. The flower is 4- or 5-corniculated (Fig. 546 B, D). The fruits have 2 pores, and are most frequently 2-lobed (Fig. 546 F, G). Some shrubs; the leaves are serrated, not needle-like. +—*Vaccinium* (Bilberry). *Whortleberry* has an urceolate, gamopetalous, only slightly developed calyx; the corolla is bilobed; the lobes are prolonged to the apex (Fig. 546). *Pyreta* idea (Gewürz) is evergreen, with flowers in racemes, and bright red berries; *R. virginica* (Bilberry) and *R. canadense* (Blueberry) have similar flowers and berries; *Vaccinium* ovalifolium has a polyglossous corolla with the petals projecting backwards. Another with appendages: *O. palustre* (Cranberry) has a slender, creeping stem, and is evergreen. Dark red berry. + +A diagram showing the structure of a bilberry flower. + +210 + +DICOTYLEDONES. + +Pollination essentially the same as the preceding order.—320 species ; espe- +cially in N. Am. Some are useful on account of their edible fruits, especially +Ficus, Morus, and the figs, and in a few genera leguminous, etc. +The fruits of F. arnottii are effective. + +A diagram showing the parts of a flower. +Fig. 546.—Ficus carpinifolia (syn. *edulis*). The parts of the flower A-E are enlarged 5-6 times ; C and E are longitudinal sections ; I and B the flower seen from above ; F and G a section seen from the back and front ; H the style and stigma. + +Family 72. Diospyrme. + +The flowers are regular, gamopetalous, typically diptosemous, +with the same number throughout all 5 whorls; thus : Sn, Pn, +An-n, Gn, where n most frequently = 5 (4-6), rarely 3, 4 or 8. +Of the 320 species belonging to this family, only a few are infertile +present only as rudiments or is entirely suppressed, and the com- +pletely developed stamens are thus placed opposite the petals. +The carpels are generally placed opposite the sepals. The corolla +is multilobed with the ovules attached in the inner angle. The +fruit is a berry or a drupe; it is usually large and large, generally solitary, or a few in each locale.—All plants belonging to this +family are trees or shrubs with scattered, single, most frequently +captive, penultimate and leafy berries without stipules; the ma- +jority are natives of America (America, Asia), some are found in N. Am. and +the Mediterranean. + +Order 1 Sapotaceae. Plants with latex; anthers extreme; 1 ovule visible +in each loculus; fruit a berry; the seeds with bony, shiny brown testsa with +large, lateral hilum. The leaves are frequently covered with silky hairs—A + +210 + +**DISPERPIUM.** — **PINELIN.** 311 + +useful order in several respects (400 tropical species). The wood of some genera, such as Siderocarpus (Iron-wood) and Eucalyptus, is as hard as iron. The following are very delicate fruits: *Lecanora* menziesii, *Achaea sepala*, *Chamaecyparis* × **Pinelina** (Pinelina × Chamaecyparis), which contains a large quantity of fatty oil. *Indomera*, *Indomera schaeferi* are often found. + +Order I. Ebenaceae. Plants without laterals, often dioecious; flowers with a more or less leathery perianth. The number of stamens is sometimes increased (400 species); sometimes reduced to two (200 species); sometimes absent (200 species); chary: tropical. Some are well known on account of their hard and black-coloured heart-wood; e.g. *Mabe* elaeos (the Molucca) and *Disporum* × **Pinelina** (Pinelina × Disporum), which contain a large quantity of fatty oil. *Ebenus* × **Pinelina** (Pinelina × Ebenus), which is cultivated as an ornamental shrub, together with other similar species. + +Only one genus, *Ebenus*, is represented in the late epigone, and the corolla is almost petaloidous. The stamens (by splitting) are more than double the number of petals; the carpels are numerous, and the seeds numerous. —351 species: Tropical Asia and America, a few for example in the East— **Official**: Gum: *Ebenus* from *Strymon* feminae and perhaps other species (*Eumenis* and *Athena*). *Hedera terebrata* (N. Am.) is an ornamental shrub with a large fruit. + +Family 28. Primuline. + +The flowers are regular, 2♀, hygogamous, and gamopetalous. + +The stamens are equal in number to the petals (Fig. 547) and are placed opposite the petals; they are inserted at the base of the petals, or free, central phallic with a many-ovules—the flower is a further de- +velopment of the Disperpium; the suppression of the calyx- +stamens, which commenced in this family, being continued in the majority of cases no trace of them is present, but in certain species and genera (*Samolus*, *Lygodium*, *Thyrsanthus*, *Soldanella*, certain Myrmeceae) some stamens remain suppressed in the position of the suppressed stamens. Again, the lateral portions of the carpels are suppressed, so that the central portion with its lateral portions are united into a free central phallic; this theory is supported by the branching of the vascular bundles, the development, and various comparative considerations.—See: Pa., A0 & Gn., where it is 4♀, +generally 5♀. The carpels are placed opposite the sepals (Fig. 547). + +A diagram showing the structure of a flower in the Primuline family. +547 + +512 + +DIOTYLEDONES. + +Order 1. Primulaceæ (Primroses). This order has many +ovules attached to a thick, free, central placenta (Fig. 547); style +shorter than the ovary ; ovules semi-antiparous ; fruit a capsule with many seeds. +The plants belonging to this order are mostly glabrous, +waning ; the flower is most frequently 5-merous (Ss, P5, +A0+5, G5) ; except Centaurea (with 3 sepals), the corolla +and capsule have very few stamens but the capsule generally opens by teeth at the apex. The +flowers are heteromorphous (Hottentot that are anatropous), +and the seeds are therefore +pellate, with the hilum situated in the centre of one side. The +endodermis is flabby or horny. The flowers are borne either in +rosettes or in spikes ; cyme branching does not occur. + +*Primula* (Primrose) has most frequently a vertical rhizome, +bearing a rosette of leaves at its summit, and long-stalked umbels; +corolla rotate or slightly funnel-shaped; style shortening +the apex by teeth. +The flowers in some species are hetero- +morphous (Hottentot) or short-styled; (Fig. +548). Closely allied are *Andrena* (with +long-stalked corolla-tube and figular scales, alter- +nating with the petals) and *Solanella* (funnel- +shaped corolla with +facinate lobes and +peltate leaves and +more frequently ligular scales).—*Hottentot* (Water-Violet) is an +aquatic plant with pectinate leaves and + + +A diagram showing three different views of a flower, labeled n, b, g. + + + +A plant with long stalked umbels and rosette of leaves at the summit. + + +**PRIMULACEAE** + +513 + +*Coriuna.* *Dodecatheon.* *Cyclamen* (Fig. 549) has solitary, long-stalked flowers, and a rotate corolla with the lobes reflexed; the stalk of the capsule runs up spirally; the tuberous rhizome is forked at the base, and produces several flower-stalks; the leaves are pinnate; *Lysimachia* (Money-wort); stem-internodes well developed, leaves opposite or verticillate, calyx almost polysepalous, corolla deeply 5-partite (Fig. 550). The flowers are solitary or few- (e.g., *Anemone* (Pineapple), *Primula* (Primrose)); the fruit is a pyxisidum (Fig. 551); similarly in *Centaurium*, which is 4-merous. + +*Trientalis,* the flowers are most frequently 7-merous—*Glaux* (Sea Milkwort) is a creeping maritime plant with opposite leaves; *Euphorbia* (Spurge) has a fleshy rootstock, and a greenish or colored calyx. The petals are usually developed later than the stamens in the Primulaceae; but in this instance they are entirely suppressed—*Saxifraga* (Brook-) + +A small green plant with a single leaf and a small flower. +Fig. 549.—*Cyclamen thapsiforme.* + +A small green plant with a single leaf and a small flower. +Fig. 550.—*Lysimachia thapsiforme.* + +weed differs from all the others in having an epigynous flower; barren stem-stamens are also present. The bracts in the racemose-flowered plants are often persistent. + +**Pollination:** Insect-pollination is the majority; cross-pollination is pro- +moted in some by heterostyly (Fig. 549)—300 species; especially in northern temperate zones; the majority on montane (Saxifraga, Androsace, etc.); also in tropical forests (e.g., *Pieris* auricula [the Alps], *P. floribunda* [China], *Forsythia* [Ornith's, a native] and *Graffioara*, etc.; *Cyclamen europaeum* [Alpine Violet]; the tubers are +Order 2. *Myricaceae.* Trees shrubs; evergreen, tropical Primulaceae with yellow flowers. The flowers are usually without petals; the sepals are nearly always dotted with yellow glands (resembling many re-septaloid) 150 species; especially *Amorpha-ORIENTALANTHUS*: *Ardisia crenata* [W. India]; other genera: *Akebia*, *Aristolochia*, *Bignonia*, *Bryophyllum*, *Ceratostigma*, *Diospyros*, *Euonymus*, *Juncus*, *Juncus erectus*, etc.—*Epipactis*, allied to this order, comprises +reflexed plants, often growing with *Euphorbia* in tropical forests, along +the shore. The embryo germinates while still in the fruit. + +514 +DORITTELEOGENES. + +Order 3. Plumbaginaceae. This order has a position of the stamens similar to that in Primulaceae (Ss, P5, A9+5, G0), but it differs from them in having the corolla tubular, the calyx somewhat dry, thin, coloured, folded, almost entire only and an almost entirely polypetalous corolla, which, as a rule, has twisted insertion and is only united with the stamens at its base; but more especially it differs from them in having the stamens inserted on the corolla and only 1 total ovule with a long, twisted funicle (the placenta of the Primulaceae is here so much reduced that it bears only 1 ovule). The fruit is a nut or capsule. The radicle is turned outwards. Euphorbiae seem to this order belong herbs or under-shrubs, which usually have opposite leaves; they are often glabrous; otherwise they also resemble the Primulaceae in the scattered, undivided, entire leaves (without stipules), often in rosettes, and the inflorescence borne on a long stalk. In opposition to the Primulaceae, the bract is not deeply persistent, and hence the branching is generally synose (scopoid). + +Armeria (Thrift) is a round capitulum, composed of closely-packed dichasia, surrounded at its base by an involucre with persistent perianth parts. The perianth is a sheath protecting the intercalary zone of growth. The pericarp is finally ruptured at the base, and drops off like a hood.--In Stachys (Lavender), the unipared scrophium cyrena are pro-longed and persistently attached to the stem. They are similar to the same which approaches nearest to the Primulaceae, and differ most from the characters given above. It has capitula or spike-like inflorescences, a single-seeded fruit with a short funicle. The style is simple. The style is only divided at the extremity; the calyx is not membranous, but is covered with sticky, glandular hairs. + +Egg plants (Solanum) are common in gardens and about the Caspian Sea, on salt-steppe and beaches. Some are tropical; a few are ornamental plants. + +B. Tetracycliceae with hypogynous flowers. + +Family 9. Tubiflorae + +The flower is regular, $\varphi$, and hypogynous. The gamopetalous type is present in this family; i.e., uniformity, without supression or splitting; S5, P5, A5, G2 (3-5). The stamens are all fertile, alternating with the lobes of the corolla. Gymnoceum with 2, more seldom 3-symporous carpels. Style nearly always simple; 2 dorsal stigmas. In each carpel 2-3 ovules. At the base of the + +**TENILORE.** 513 + +ovary is found a yellowish ring-like nectary (Fig. 552 C), sometimes stipulate or 5-partite. —The leaves are nearly always scattered; stipules are absent.—The flowers are usually solitary, but in some cases, are so closely allied to the *Pentomea*, that it would be unnatural not to place them firm in this family; and the *Bursaginaceae* (which were also placed in the *TENILOREAE* by some botanists) are now considered a distinct family. + +Order **Corylaceae.** *Pterocarya*. The flowers are regular; L. P., A5, A6, B2. The calyx and corolla have united leaves, the petals related to the right in *exstria* (all the left edges being covered). The corolla is boudaried with 2-5 ovate lobes in one plane, and is followed by a long tube, which is prolonged into a capitate Enlongate style; endocarp thin. The inflorescence is dichasia passing over into unifoliate helical cyme (the shoot of the lower bracteole being the axis of the upper one); the peduncle is short, and is often very slender; especially Western N. Am.—Phales (wholly scapular corolla; entire, opposite leaves), Polemonium (companion or almost alternate corolla; sessile, pinnate leaves), Lonicera (wholly scapular corolla; entire, opposite leaves), and *Eriogonum* (tendril at the ends of the leaves), etc. They are frequently ornamental plants. + +Order **Boraginaceae.** *Borago*. The flowers are regular; L. P., A5, A6, G2. The lobes of the corolla are imbricate in maturation. Green 2 median veins pass through the middle of each lobe, and two lateral veins extend on 2 parallel pleurae; capsule 2-valved; enlongate style; endocarp thin. In the corolla-tube, opposite the corolla-lobes, there are frequently appendages of various kinds, which correspond exactly with those of the *Bursaginaceae*, being unpaired cypers, which, prior to opening, are tightly rolled up.—Lysimachia, especially L. europaea (with a bilocular ovary), L. vulgaris (with a trilocular ovary), *Walterisia*, *Enockia*, *Cassiopea*, etc., are cultivated in gardens as ornamental plants. Hydrastis has a bilocular ovary, and two free styles. + +Order **Convulvulaceae (Bindweed).** The flower is regular, hypogynous, with a almost free sepals (quincuncial insertion), P., A5, G2 (nearly 3–5). The corolla is very characteristic; it is (usually) 5-lobed or 3-lobed, and folded longitudinally to the fold in such a manner that the outer portion is erecting, flat portions, tapering towards the top and frequently differing in colour and hairiness from the rest, are visible externally and applied together to form a tube; when the flower is folded together (Fig. 552 A) and hence the whole corolla is closely twisted to the right in the bud. The crocosmum most frequently has a bilocular ovary; in each locusus there are only 2 (rectang) anatropose ovules on the placenta, which is not especially thickened (Fig. 552 D,E); each loculus is somewhat divided into two false septum (a relationship with the *Boraginaceae*, can be style simple with + +516 +**Dicotyledones.** + +most frequently a bilobed stigma, or a bispinate style. The fruit is usually spherical, most frequently a capsule. The seeds are erect, and have a large hilum at the base. The embryo is curved, with leaf-like, thin, bilobed, most frequently folded cotyledons; endo- +spor absent or maculate. + +1. **Cucurbita** (Burdock Genus). The majority are twining (to the left) herbs, with leaves. The leaves are scattered, without stipules, often long-stalked, and nearly always with cordate base; some are palmately lobed. The flowers are most frequently solitary in the inflorescence (Fig. 533), but sometimes in cymes (Fig. 532). **Calpogynium** (unilocular ovary, 2 large bracteoles), *Ipomoea* (Malvales), *Evolouise* (with a doubly bifid style), *Calycogynium*, *Pharbitis*, etc. + +A B C D E +Fig. 612.—Cucurbita communis. + +2. **Dioscorea**. This group is a more primitive form, not twining, and without latex. It has a free corolla with basal style (as in Borraccinaceae) and valvate corolla. + +3. **Cucurbita**. *Dioscorea* (Genus). Parasites, with round, filamentous stems, bearing only scale-like leaves and almost destitute of chlorophyll (they are reddish or yellowish); they are parasitic upon other plants, around which they twine, first with narrow, compact coils from which haustoria (Fig. 533 A) are developed which penetrate the host's roots, and then by means of which they raise themselves to other portions of their host or try to reach other plants. On germination a very primary root is developed, which bears root-hairs as far as the tip (root- +cap is wanting); it only serves as a kind of reservoir for water, and perishes very soon after the seedling has fastened on to a host. +The embryo is filamentous and curled up generally (Figs. 533 C), and + +PERSONATUM. 517 + +is sometimes destitute of cotyledons. The flowers are crowded into capitulate inflorescences, complicated by accessory bracts (Fig. 533 A); they have S5, P5 (entomocentra motitation), A5 (and beneath the stamens 5 scales on the corolla-tube), G2. Fruit a capsule opening by a lid—Oncostea europaea, C. epilobium (Flax-Dodder), C. ciliata, C. ciliata subsp. Boudieri, or Lycium (Cobweb-Dodder), etc., are parasitic on different hosts, or parasitic each on its own particular host. + +A small plant with yellowish-green leaves and a small yellow flower. + +Fig. 533.—Oncostea trilobii, parasitic on Red Clover. A portion of the stem with an interseccus and laminae (thick); B seed (tan, thin); C seed (red); D embryo (pink). + +840 species; the majority in the Tropics, especially Am. Many are ornamental plants. Ornamental: some on account of their purgative properties : the whole plant is used in the treatment of dyspepsia and constipation; the latex ("Summation") of Convolvulus scouleri (from the East). The tuberous roots of *Bastard edible* (Trop. S. Am.) are used as a common vegetable (Sweet Potato) in the tropics. + +Family 30. Personatum. +The type of the flower is: S5, P5, A5 (of which one, or in some cases several, are suppressed), and G2. The flowers are + +518 + +**DIOTYLOLEONES.** + +**Agyopogon,** 3, perfect with gamopetalous corolla, but most fre- +quently irregular (medianly symmorphic, except *Solanceae*), the **corolla** being bilabiate (divided into a posterior part of two lobes and an anterior part of three lobes), and the stamens 4, dillinamous (the petaloid stamens being reduced to filaments only); in *Urticariaceae*, *Genistaeeae*, *Orchideae*; the placentas in the first-named orders (1–7) is most frequently very thick, and bears a great many ovules (Fig. 554, 555, 557, 562); the number of ovales in the last-named order is usually one. + +Special mention may be made of the apparently 4-merous flower which is found, e.g. in *Fernoxis* and *Fatsia* (Figgs. 567, 562C, 571, 571), and which arises from the typical 5-merous flower by the loss of one of the lateral petals, and by the reduction of the lateral stamen, and by the union of the two posterior petals into one—Terminal flowers very seldom occur on the main axis, and would not harmonise well with the very irregular form of the flower. + +When they do occur on the main axis, they are often found on *Liriope vulgaris* two kinds of peltate flowers occur—one with 5 spurs, and one without spur). The halves of the anthers are often divided as far as the base, and laterally so widely separated from each other as to appear like two separate anthers (Fig. 563, 564). There is generally a nectary ('disc' ring) round the base of the corolla, often folded (or divided into free glands), a common vegetative characteristic is the absence of stipules. + +The 8 orders of the Peptomata are: 1, Solanceae; 2, Nolanceae; 3, Scrophu- +lariae; 4, Liliaceae; 5, Amaryllidaceae; 6, Gentianaceae; 7, Polygonaceae; 8, Phebeaceae; 9, Aristolochiaceae. + +Order I. *Solanceae.* The flower (Figgs. 554, 555, 559) is hypogynous, regular (symmorphic in *Hyoscyamus*), 3, and gamo- +petalous, with sepals (which are frequently imbricated or overlapping), A5, G2 or G3. The cor- +pels being placed obliquely (Fig. 554); the bilocular ovary has a very thick axile placenta (Figgs. 554a, 555 H, 557), which is surrounded by a thickened wall around its base—the ovary. The fruit is a capsule or berry; the seeds are more or less reniform, and the testa thin (Fig. 560). + +**Pis. akk.—Diogenus of Fatsia.** + +A diagram showing a flower with a bilocular ovary and a thickened wall around its base. +A diagram showing a flower with a thickened wall around its base. + +PERSONATE. + +but with variously formed laminae (always pinnatisect), a peculiar leaf-arrangement is found in many species, viz., the leaves are borne in pairs, a large and a smaller one together ; these pairs stand in 2 rows, and the flowers are then situated between the middle of the two leaves of each pair, at the leaf axil. The inflorescences are frequently unipared scorpion-like, without floral-leaves. + +A diagram showing the arrangement of leaves and flowers in a plant with a peculiar leaf-arrangement. +A B C D E F G H I J K L M N O P Q R S T U V W X Y Z + +319 + +Fig. 555.—*Drostea helldamnus*. *A* is reduced. + +Zygomorphic flowers occur, and they form a transition to the closely allied Scrophulariaceae; the zygomorphy sometimes shows itself only in the relative length of the stamens, sometimes also in the corolla (*Hephaestus*)—Nemobdus is an example of this. A peculiarity of the leaf-arrangement in this order occurs from sympodial branching and displacement. The most simple is, e.g. *Datura* (Fig. 556 d); here the leaves are on the dorsal parts of the stem, and the first shoot has 2 (and 3?) leaves, and then numerous flower stalks arise from them. In *Catharanthus* (Fig. 556 f) almost so far, as the first leaf of these axillary-shoots, the flowers are borne singly on the dichasial branches, and all the branches appear to be without embedding leaves (though they may have them). In *Drostea*, however, the leaves differ (Fig. 556 B) differ in that the smallest and smallest ($f$) of the two leaves on each shoot is barren, and is therefore not displaced; but the upper one (the second shoot) bears 2 flowers, which are placed at right angles to each other; consequently it assumes a position near the first leaf (the shaded leaf $f^{\prime}$ of shoot II being placed near the white leaf $j^{\prime}$ of shoot II, etc.) of the next youngest shoot-generation, + +A diagram showing the arrangement of leaves and flowers in *Drostea helldamnus*. + +520 + +DICOTYLEDONES. + +and hence the leaves are borne in pairs; the flower placed between the two leaves of a pair is therefore the terminal flower of the shoot to which the number of the two leaves belongs, and the larger leaf is the subtending leaf for the lower shoot itself. + +A diagrammatic representation of the branching in Solanum. The various shoot-generations are white or shaded. + +A. Fruit a CAPULE. Nicotiana (Tobacco) has a 2-valved capsule with a narrow, delaminate calyx, which is separate at the apex; the corolla is funnel-shaped, tubular, salver-shaped or campanulate. The flowers in panicles.—Datura (D. stramonium, Thorn-apple) has a (frequently spiny) capsule (Fig. 553), which is + +Diagram of Datura stramonium showing the fruit and corolla. + +B. Fruit of Hyoscyamus niger after +fully-4-lobed (at the top, bilobate) and opens septifragally with +4 valves. The lower part of the calyx persists as a thick collar + +PERSICACEAE. 521 + +(see Fig. 558). The corolla is funnel-shaped. The flowers are solitary, large, --Hypocymus (H. nigrescens) has a pyramidal (Fig. 557) enclosed in the campanulate, completely persistent, thick-walled calyx. The flowers are slightly zygomorphic, and borne in unpaired acrospetal cyms. Sapote (pyramid); Foliacea (pyramid); Pachysandra (pyramid); Saururus (pyramid); Acanthopetalum (pyramid; corolla); Nierembergia; Bravetilla (apical a droop); Fraxinaceae; Broussilieae. + +Among those with capitate fruits are found the most anomalous forms, the Lycium (fig. 559), which have a conspicuous stamens present the transition to the Serophylaraceae; Salpig- loine; Schizanthus (Jobed petals; 2 perfect; and 3 rudimentary stamens). + +B. SUBT. A DERRY. Solanaceae (Nightshade); rotate corolla (Fig. 550). The stamens have short filaments, the anthers stand erect, close together round the style, like a cone in the + +Fig. 550.—Solanum tuberosum. +Fig. 551.—Flower (). +Fig. 568.—Stamen, showing pollen. + +centre of the flower, and open by pores at the apex (Fig. 550). S. tuberosum (the Potato plant); the Potatocactus is a sepal, underground stem; the "eyes" are bud-like leaves, which are quickly petiolarized; the numerous resembles Solanum in the flower, but the united anthers open by longitudinal clefts and have an apical appendage. The cultivated species, L. esculentum (Tomato), has an higher number of stamens than the wild form, several being united into a tube; --Phytolacca (Winter Cherry); the calyx ultimately swells out in the form of a bladder, becomes coloured, and loosely envelops the spherical berry.--Cupuacu (Guinna Pepper- plant); --Lycium (fig. 559); --Lycium (fig. 560); --Lycium (red, yellow, black) berries, which are unicellular in the upper part--; Lygoua (false Tea Tree); the corolla is salver- or fannel-shaped; shrubs; often thorny.--Atropa (A. belladonna, Deadly Nightshade, + +521 + +522 + +**DOCYLEDONACEAE.** + +Fig. 553; corolla campanulate; the calyx projects beneath the spherical black berry. The flowers are borne singly—*Manduca*—or in clusters—*Nicotiana* (often out-of-bloom).——A small tropical genus, consisting of about 100 species, mostly of the Old World, only one of which may be found at e.g. in sections Nicotiana. Related to the *Sero- +phylaceae.* + +About 10 genera spread the diversity within the family, outside these limits especially in America. *Solanum nitidum* is a common weed—the *Potato-plant* (*Solanum tuberosum*, from Peru and Chile), was introduced into Europe in 1864 by Sir Walter Scott, who had planted it on his estate at Abbotsford. It is a common weed—*Chillies* or Pod-piper (*Capsicum annuum* and *Capsicum frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. baccatum* and *C. frutescens*) and the Cayenne pepper (*C. +1 + +**FEROXALE.** 523 + +spooking, no characteristic feature which absolutely separates them. The somewhat irregular corolla, with five segments of unequal length in Ferocactus, is also found in Euphorbiaceae; curved and straight corollae are found in both orders. The extension of the corolla to the Sempervivaceae is simply decorative. + +A diagram showing the structure of a Ferocactus flower. + +A. Ferocactus. +B. Lonicera. +C. Vernonia. + +In the Sempervivaceae most frequently folded corolla (in Atriplex and those allied to it), labellum (in Euphorbia) are found. These may be distinguished according to the form of the corolla, number of stamens, inflorescence, arrangement of the leaves, etc. Ferocacti belongs to the most primitive 5-stamened group, from which the other groups have arisen, but only two stamens and most frequently the posterior stamen suppressed. + +I. **ANTHRAXIS, SNAPDRAGON GROUP.** This has most frequently a descending insertion of the petals (the posterior petals being usually lateral ones, which again enclose the anterior; Fig. 562 A, B). The plants belonging to this group are mostly 5-stamened. + +5-stamened — *Ferocactus* (Muell., Fig. 563 A) has a slightly irregular, rotund or conical corolla, 5-stamened (frequently covered with woolly hairs), of which the two anterior ones are the longer and more conspicuous than the others, and in each respect. The inflorescences are racemose, often with several flowers on one stem; they are usually oblong in the axil of each primary leaf-foil. The leaves are scale-like, linear or ovate-lanceolate; the stems, are often covered with a grey felt of branched hairs. + +A Ferocactus flower with its corolla. +A Ferocactus flower with its corolla. +A Ferocactus flower with its corolla. +A Ferocactus flower with its corolla. + +Fig. 563.—*Ferocactus thurberi.* + +524 + +DECOTYLEDONAE. + +b. 4-stamened, didynamous (Fig. 564).—*Scrophulariae* (Fig-wort, Fig. 565) has cymose inflorescences in a panicle; the corolla (Fig. 565) is urceolate, short two-lipped, the posterior stamens are present as a scale below the upper lip of the corolla (Fig. 565).—*Scrophularia* is a tuberous rhizome.—*Pedicellum*: the posterior stamens are long and very long.—*Astrantia*: (Snapdragon). The corolla (Fig. 564) is personate, i.e. bilabiate, but with the + +A flower and the upper lip of a flower with the stamens. +Fig. 564.—*Astrantia major*. A flower, and the upper lip of a flower with the stamens. + +A flower with a two-lipped corolla. +Fig. 565.—*Scrophularia purpurea*. + +A flower with a two-lipped corolla. +Fig. 565.—*Scrophularia nodosa*. Protogynous flower in various stages: *A*♀ stage; *2*♂ stigmas projecting from the throat of the corolla; *3* the same in longitudinal section; *4* anther of one of the stamens; *5* anther of another stamen; *6* anther of a staminode; *7* stigma; *8* anther. + +under lip arched to such an extent that meets the upper lip, closed the corolla throat, and entirely conceals the stamens and + +PERSONATE. 525 + +style; the corolla-tube is prolonged into a short pouch at the base on the anterior side. The capsule is oblique and open by 2-3 pores, formed by small, dentate valves. In *Limaria* (Tond-bux) the perianth is persistent, but the corolla-tube is prolonged into a pouch of the posterior stamens. The capsule opens by large pores (one for each loculus), produced by large, many-partite valves. *L. europaea* reproduces by suckers.—*Diplaxis* (Foxglove, Fig. 560) + +The lower lip of the corolla is usually long and narrow, or small (a step towards complete suppression, as in *Veronica*) ; the corolla is obliquely campanulate, and generally nearly 4-lobed, the two posterior petals conalineous.—*Alchemilla* : *Nemophila* : *Chelone* : *Fatsia* : *Cerastium* : *Saxifraga* : *Potentilla* : *Mud-wort, native* ; *Scoparia* : *Capraria* : *Erinus* (found on the Roman Camp at Chester, Northumberland, and supposed to have been introduced from Spain by the Roman soldiers) : *Celisia* (near *Veronica*) : *Murumundus* : *Lepidophyllum* : *Echidnaceae* : *Callicoma* : *Nyctemera* + +c. 2-stamened - *Gratiola* (Water-hypox). - 3-partite calyx. + +The upper lip of the corolla is undivided or bifidly lipped; the lower lip is divided into two lips, one of which is entirely absent or are reduced to staminodes (a transition to *Veronica*)— +*Veronica* (Speedwell), most frequently 3-partite calyx; 4-lobed calyx, 3-lobed corolla, morphologically like a perfect stamens and no trace of the others (Fig., 567, 562 o); capsule with localised de- +veloped stamens; the corolla has two stipule-like lips. + +d. 2-rhinanthoid - *Yellow-battle* + +GROUP. Herbs, all of which (with the exception of *Lathyrus*) are annuals or biennials with green foliage- +leaves. The flowers are themselves by haustoria to the roots of other plants and draw nourishment from them. The majority turn black when dried. Racemose inflorescence. In many the calyx is 4-partite, the posterior petals conalineous. — The corolla is 4-partite, with white base (Fig., 568), with most frequently ascend- +ing catenation; in the majority its base does not become detached at the base, but by means of a ring-like cut some distance up the tube; a 4-divinuous stamina; pollen-grains dry, easily falling out; the anthers are often furnished at the base with bristles or hairs (Fig.) + +506 + +SUCULETENES. + +506) which play a part in the pollination, the prothecia of the insects, being forcibly pressed against them, agitate the anthora and shake out the pollen-grain. Capsule with localiocal disheavenece. +—Raphesia (Ivy-bright), Melampyrum (Cow-whisk). *Echinacea* (Yellow-rattle), *Odonata* (Bartian). *Podocarina* (Louse-wort), *Lathyrus* (Tooth-wort) are such species. The last named is pale yellow, velvety (without chalazae), and has its roots of the Hazel, Beech and other shrubs, having an aerial stem, and an underground, perennial rhizome, covered with opposite, scale-like, more or less deeply furrowed leaves. The flowers are solitary. The inflorescence is a unilateral raceme. It approaches *Grewia* in having a unilocular ovary with two parietal placentae. + +A diagram showing the structure of a flower and the anther and stigma. + +Fig. 506.—*Euphrasia officinalis*. Flower of the large and the small-flowered forms; showing the anthers and stigma. + +The nature of the prothecia for *Podocarina* are so different that no general principle can be laid down. Personal flowers, like those of *Antirrhinum* ramosum are only accessible to certain insects, such as humble-bees, which can force their way through the chalazae and take up the pollen-grain from the back. In *Euphrasia* and other *Echinaceae* the insects become covered with smooth, powdery pollen when they shake the anthora-apparatus in touching the back and hanging over it. The flowers are solitary. The stamens (Fig. 565). *Digitalis purpurea*, however, is protracted. Membranous leaves and some others have sensitive stipulate lobes, which shoot up on being touched. The *Veronica* species are also interesting in this respect. They have various forms, and parallel with them are found various gradations from insect- to self-pollination. In *Veronica* (at least in its European species) there are two kinds of flowers: large, which are pollinated by insects, and small, which are self-pollinated (Fig. 568). *Lathyrus auriculatus* is a pro- +liginous spring-flowering plant, largely valued by humble-bees. Others have dichogamous flowers. *Nepitella aurea* opens its flowers at night. + +507 + +**FEROXIAE.** 527 + +2,000 species; chiefly from the Temp. *Original:* Diphylleae purpurea (the leaves); Europe), a poisonous plant. *Ferocactus* thyraceus and *thyraceus*, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* thyraceus, *Ferocactus* th yraceseu + +Order & Utriculariacea. To this order belong only pur- cennial, anectivorum aquaticum and search-plants (200 species) with a more or less characteristic appearance. They differ from the Scrophulariacea especially in having 2 stamens (the anterior) and a well-closed corolla with free central placenta (like that of the W. H. + +Fig. 86.—Leaf of Utricularia vulgaris with bladder. Median longitudinal section through a bladder containing water. The bladder is seen in two planes: an in a section of the under-tip of the mesicra (a., b.), in the latter are placed 4 bristles ; a stalk of the bladder is shown in c. +Order & Utriculariacea. To this order belong only pur- cennial aquaticum and search-plants (200 species) with a more or less characteristic appearance. They differ from the Scrophulariacea especially in having 2 stamens (the anterior) and a well-closed corolla with free central placenta (like that of the W. H. + +528 + +**Decotyledons.** + +*Primulaceae.* For the rest the flower is distinctly bilabiate, both in the calyx and corolla. Two-valved capsule; no endosperm. + +*Pinguicula* (Butter-wort) has a rosette of leaves close to the ground; they are usually green, but some species have a white or yellow roll round any small insects which may be caught upon them; flowers solitary, terminal on a long scape; calyx, 5-partite; corolla with spur. The embryo germinates with 1 cotyledon. *Utricularia* (Hindoo-calamari) is a genus of aquatic plants, with hair-like divided leaves, studded with peculiar bladders (in the Tropics there are terrestrial species, with ordinary foliage). The bladders (fig. 509) have an aperture, closed by a valve opening inwardly, so that the water in which they are allowed to enter, lest they not able to escape; they are thus entirely protected from evaporation, and are probably used as food. Calyx bipyrate; corolla personate with spur. + +The entry of *Utricularia* is very important, especially more than a spherical calyces much less a few short leaves. On the germination of *U. vulgaris*, numerous bristle-like leaves develop into a compact rosette; the stem then develops, and also the finely-divided, bladder-bearing leaves. A primary root is not formed, but a secondary one grows up in a spiral manner. The growing-point of the stem is rolled spirally—The stipulate leaves are sensitive and close on being touched—self-pollination often takes place, however, in this case. + +Order 5. *Gennaceae.* The flower in this order may be both epigynous (in *Gennaria*) and hypogynous (in *Ceratostigma*), but generally it is hypogynous. In *Saxifraga*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. In *Saxifraga*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. In *Saxifraga*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. In *Saxifraga*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. In *Saxifraga*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. In *Saxifraga*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in *Ceratostigma* it is persistent together with the petals. + +In *Gennaria* and *Astrantia*, only the calyx is persistent, but in + +528 + +**FEUERZOLL** + +529 + +brunches with hastulae, but growing with the base of its stem in close contact +with its leaf, and probably even over extending a little into its axis, a form +similar to the Lathraeaeanum. Its aerial shoots are not entirely destitute of +chlorophyll, but are not green; they only bear scale-leaves and terminus in +a manner similar to that of the Lathraeaeanum. The flowers are also reminiscent +of various cultivated plants (Hemp, Lucerne, Tobacco, etc.). The flowers are +arranged in cymes, which are very numerous and very small, and are attached +united to the two lateral ones. Ovary unilocular, as in Gomphrena, with 8 or +4 pappal stamens.—The exceedingly small leaves have a very rudimentary +stem, and are covered with a dense pubescence. The leaves are simple, linear, +or oblong—about 100 species; especially in the Mediterranean region. +Order 6. Bignoniaceae. 1000 species; nearly all trees and shrubs, and to a +great extent climbing plants. The leaves are simple, entire, or serrate, sometimes +terminated by a special clapping apparatus. These lines have as a rule, an anomalous stem structure, the wood being either divided into four wedges at right angles (as in the Bignonia), or having a single central vein, or a more or less +paenysymal, or a greater number of wedges occur, by the cambium ceasing to +form wood in several places. The leaves are most frequently opposite and com- +pound; but there are also many species with alternate leaves. The flowers are +numerous and usually terminal. The fruits are capsules or berries. The ornamental +plants in the tropics belong to this order. The fruit is most frequently a large, +woody, 2-valved, silique-like, capitulifugal capsule, whose valves separate +into two parts when ripe. The leaves are simple and entire; the flowers solitary or in small cymes; seeds: Tecoma: *Bignonia*—in gardenia: *Syringa* (Trumpet-wood): *Tecoma radicans* (from S. Am.)—*Pseudocodon*—used in from Zanzibar to the Generacaea (L. sceler; borthosus). + +Ceratonia is allied to the order Cercidae (Chabaud) its best known +species is *Ceratonia siliqua*, a tree resembling *Robinia pseudoacacia* in having a long +horrned ovule and sensitive stigma—46 species. + +Order 7. Pedaliaceae. Senecio (senecio and rudbeckia), very important +old plants of the family Asteraceae, used for food and medicinal purposes; +and Africa for food and as medicinal plants, and are now cultivated in America +also. The seeds are used as a raw material in the manufacture of soap in Europe. European species are rare; but some American species have a long horned ovule and sensitive stigma—46 species. + +Order 8. Xanthaceae. 1000 species; mostly erect, slender, branched +herbs or sub-shrubs; flowers white or yellowish-white; petals 3 or 5. The +branches frequently have swollen nodes; the leaves are opposite, pennate or with +undulate margins; the sepals are persistent; the petals fall off before the fruits are +formed; the fruits are capsules or berries. The flowers are ordinary or with +two bracteoles. With regard to the corolla (which is often labiate, in any +case irregular, and frequently prettily coloured), the 3 or 4 diphynous stamens + +530 +DIOTYLEDONES. +(of whose anthora one half is inserted lower than the other, or suppressed); and the gynoeceum, the Anacanthaceae are true Perennials, approaching most nearly to the Scrophulariaceae, but differing from them in having the corolla-lobes (which are 5) bilabiate; 3-valved, either entirely delibiating exapetalous, which never has more than two raves, and in some only 2 seeds in each loculus, the seeds being often very small; or with 3 valvate petals, which are either entire (or serrate) which persist after delibiation. Embryo carried without calyptrae; radicle pointed downwards—Clarioginaceae flowers are found in several species. Quercus alba. + +The following grow wild in Europe: *Anacanthus* (Cynium) and *Moluccella*, whose plume-like leaves serve as modals for the capitula of the Cornusseum columnarum. The perianth is usually 5-lobed, but sometimes 6-lobed; the sepals are often united into one part like a bilabium; the 5 lateral sepals are united, and the two lateral ones are as long as the median one; the median one is longer than the upper lip, but only a bident under-lip. The anthora are bilabiate; the lamina of the upper lip is very firm.—*Justicia*. *Eupatorium*. *Goldfussia*. *Therubieria* (a twiner). *Rutella*. *Dicentra*. *Dichroa*. *Lysimachia*. *Oenothera*. *Hylotelephium*. *Saxifraga*. + +Order 2. Plantaginaceae (Plantains). The flowers (Figs. 570, 571) are regular, 5, hypogynous, with a 4-partite, persistent calyx, a gamopetalous, serrate corolla with 4 projecting lobes, 4 stamens, inclosed in the bud, later on projecting considerably, about equal in length to the corolla; the style short, erect, simple; the ovary monoeccious, sessile, fleshy, papillose style (see Fig. 571). The ovary is most frequently bilocular with 1- few ovaries in each loculus. An hypogynous disc is wanting. The fruit is a pygidium with 1- few lateral persistent stamens in each loculus (Lettieria is in several records a pygidium). All species have herbariums with leaf-rosettes near the ground, and the flowers in spikes or cupuliform. + +The lathe-like flowers are in this case entirely enclosed under a regular, especially long petaloid calyx. In some species of *Lettieria*, as in the Scrophulariaceae, only the rudiment, which is found in *Pterocarya* (compar. Figs. 562 c), 570 with 270, 571), is also present in its instance and the lobes are as long as the corolla. In others (e.g., *Lettieria*) the calyx is only the lateral upper-lip; the posterior stamen and the posterior sepal also are entirely wanting. In the development of the flower there is no trace of posterior sepal or stamens at all. The anther is always opposite to one of the lateral anterior sepals arising before the lateral ones. The position of sepals and petals does not agree with that of atrors-merous flowers which is represented in Fig. 570. The fruit is a pygidium. + +*Plantago* (Plantain, Rib-grass). The foliage-leaves are most frequently scattered, entire, with curved veins, arranged in a rosette close to the ground on an unlimited rhizome; the spike-like inflorescence is borne on a long scape; in some (*P. platyphylla*) + +**NUCULIFER.** + +the leaves are opposite on a stem with well-developed internodes, and the inflorescences are borne in their axils. The order also presents a transition from insect-pollinated to wind-pollinated flowers. The flowers are protogynous, wind-pollinated in *P.* major and *P.* media, and insect-pollinated in *P.* trichocarpa. In *P.* trichocarpa, *P.* minor, *P.* minor var. minor, and *P.* media has three kinds of flowers, some of which are adapted for wind-pollination (fig. 87), others, with short stamina, for insect-pollination. *Latrodica* (scandens) is a plant with a long, red rootstock of the Plantaginaceae; an aquatic plant with rosettes of round, awl-like leaves and diclinous (monocious) flowers. In the axils of the foliage-leaves is a very short flowered scape bearing two flowers. The upper one is a calyced flower, and the lower one is a flower. The terminal one being absent, as in *Plantago*. The 3-flower is essentially the same as in *Plantago*, but the 7-flower has a serrated corolla, with a narrow, 3-4-dentate mouth, which closes tightly round the nutlike fruit. + + +A diagram of *Plantago major*. + + +Fig. 87.--Diagram of *Plantago major*. +87a.--Two different forms of the flower (magnified). 1, chiefly adapted for pollina- +tion by wind; 2, for insect-pollination. +The upper one is a calyced flower. + + +The genus *Plantago* constitutes nearly the entire order (300 species). Some are edible (e.g., *Plantago major*, "The white man's footstool"). In *P. pusilla* (S. Eur.) the integument of the seeds is mucilaginous, and swells considerably in water. + +Family 31. Nuculiferae. + +The flowers are hypogynous and zygomorphic (in Boraginaceae and Corallariaceae, however), and are usually perfect. Echinus and An- +chusa arcuata. The calyx is gamosepalous, the corolla bilabiate (except in the two orders mentioned), mostly four-lobed, i.e., divided into a 2-leaved posterior portion, and a 3-leaved anterior portion. + +532 + +1 + +**DICYTOYLEDONES.** + +The natation of the corolla is nearly always descending.—In *Boraginaceae* and *Carduaceae* there are 3 stamens of equal length; in the other order, only 2 stamens, or only 2 fertile, the posterior stamen is sometimes developed as a staminode, sometimes fertile (in *Sileneae*), with (-)2 ovules on each carpel; in the majority of the other orders there is a distinct partition-wall between the dorsal and ventral stamens, into 4 loculi, each of which is often raised independently, causing the style to be situated in the depression between the four lobes ("gynobase" style). Fig. 572. The fruit is usually a schizocarp, but not unlike fruits. The other orders have a (1-2)-locular ovary.—The leaves are simple, without stipules. + +The family is related (and proceeds from) the *Podostemaceae*, especially *Corynocaraceae*, which are supposed to be the nearest allies of the order. It is doubtful whether the *Corynoaceae* and *Boraginaceae* should be classed with the others. + +The orders are: 1. *Cardioideae*, 2. *Boraginaceae*, 3. *Verbenaceae*, 4. *Labiate*, 5. *Rutaceae*, 6. *Euphorbiaceae*, 7. *Caryophyllaceae*, 8. *Asteridium*, 9. *Labiatae*, 10. *Umbelliferae*, 11. *Caryophyllaceae*, 12. *Umbelliferae*, 13. *Umbelliferae*. + +Order 1. **Cardioideae**. The vegetative parts are very characteristic; leaves with cylindrical stems, sessile, unifoliate, nearly always sessile, entire leaves, without stipules, and generally, together with the other green portions of the plant, covered with stiff hairs, conspicuously rough and often even stingy (hence the other names given to this order); flowers perfect or imperfect; corolla unpaired symmetrical (the branches coiled spirally "calyce," Fig. 573) before the flowers open. The flower is perfect, regular (obliquely zygomorphic in Echium and *Androsaemum aromaticum*), hypogynous (i.e., inserted below the calyx), with one or two growths), A5, G2, but each of the two loculi of the ovary becomes divided by a false partition-wall into two, each of which contains one pendent anatropous ovule with the micropyle turned upwards; the style is long, spreading or curved outwards; ovary 4-lobed, and the style is thin in the Boraginaceae placed at the base ("gynobase") between the four projections (Figs. 572, 573). The fruit is a 4-partite schizocarp with four nut-like fructlets (Fig. 572).—Endopolyploidy is wanting (except in Heliotropium), the radicle is turned upwards. + +A diagram showing the structure of a flower in the Cardioideae order. + +NUCULIFERA. 533 + +The inflorescences are often double unipared scorpion cymes; the bud of the second bracteole is developed, that of the first suppressed; in some cases both the bracteoles are suppressed, and the flowers are arranged in two rows, sometimes all the first bracteoles (a) only are suppressed, and the others are situated in two rows towards the under side of the calyx axis, while the flowers are situated on the upper side of this axis, and are thus placed in two different positions to take place. The flowers are often red at first, and later on become blue or violet; they rarely ever have any small. The fruit entirely resembles that of the last genus, but differs in its structure. The fruits of both genera present small differences which have systematic importance; they are hollow or flat at the base, attested by a thick or echinosecospicous, etc. + +I. HELIOPTERIDEA. This group deviates from the characteristics mentioned above in the undivided ovary and terminal ("apical") style. In this genus, as in *Heliotropium* (Heliotrope), *Echino- fortis*, *Eleutherococcus*, etc. the fruit is a drupe, it connects this order with the Cordiceae. Heliotropium, Tiarella, and others have schizocarpus. + +A. The thorn of the corolla is without ligules, or with very small ones.—*Palmarosa* (Langwort); funnel-shaped corolla; a whorl of hairs in the corolla-throat.—*Echium* (Viper's-bugloss) has sycomorous flowers; the corolla is divided into four segments, containing with them a well-developed inflorescence (through the fourth segal); the corolla is obliquely funnel-shaped; the style is more deeply cleft at the apex than in the others; stamens 2 longer, 2 shorter; petals 5 broad, 5 narrow; sepals 5 broad, 5 narrow; fruits five small teeth and two bilocular fruitlets. The bracts are large and leafy, and, like all the rest of the plant, are almost glabrous.—A few *Lithophragma* species have a naked corolla-throat; other species have a short calyx-throat which closes the opening of the corolla. These fruitlets are as hard as stone, owing to the presence of calcareate of lime and silica.—*Mertensia* (Stem- hammeria); *Arabis* (Noumea [small lingua]). + +B. The corolla-throat is closed in one case provided with long, hair-like body or small or pedunculate, situated in the throat of the corolla opposite the petals, and which are invaginations or internal spurs of the petals (Fig. 572 A)—The nuts in *Gymnolobium* (Hairy-loblolly) are enclosed by a calyx-throat which covers the entire corolla—*Echium*—echinosemum, only on the edge. The following have smooth nuts.—Symphytum (Comfrey) has a cylindri- cial, campanulate corolla, and prolonged-triangular, pointed ligules.—*Borage* (Borage) has a rotate corolla with projecting, + +A diagram showing a flower with a calyx-throat. + +534 + +20COTYLEDONES. + +emarginate ligules; the stamens have a horn-like appendage, pro- +jecting upwards from the back of the filament. The fruitlets are +hollow below—(Akanthus, Fig. 372). The corolla is +salver-shaped; the ligules are long, with a terminal lobe (Lyc- +opus) arrense has an S-curved corolla tube.—Myosotis (Forget- +me-not, Fig. 373); rotate corolla with small (yellow) protuber- +ances in the throat; scrophulary stem without floral-leaves; fruitlets + + +A - Acanthus ilicifolius. A diagram, the bracteole b is suppressed (thinned). +B - Myosotis, the fruit, entire and with the calyx in longitudinal section. +C - Ageratina, the corolla opened (?); the ligule f is the stamens; +D - Erythronium, the corolla opened (?); the ligule f is the stamens. +E - Ophrys, the corolla opened (?); the ligule f is the stamens. +F - Ophryanthus, the corolla opened (?); the ligule f is the stamens. +G - Asclepias, the corolla opened (?); the ligule f is the stamens. +H - Asclepias, the corolla opened (?); the ligule f is the stamens. +I - Asclepias, the corolla opened (?); the ligule f is the stamens. +J - Asclepias, the corolla opened (?); the ligule f is the stamens. +K - Asclepias, the corolla opened (?); the ligule f is the stamens. +L - Asclepias, the corolla opened (?); the ligule f is the stamens. +M - Asclepias, the corolla opened (?); the ligule f is the stamens. +N - Asclepias, the corolla opened (?); the ligule f is the stamens. +O - Asclepias, the corolla opened (?); the ligule f is the stamens. +P - Asclepias, the corolla opened (?); the ligule f is the stamens. +Q - Asclepias, the corolla opened (?); the ligule f is the stamens. +R - Asclepias, the corolla opened (?); the ligule f is the stamens. +S - Asclepias, the corolla opened (?); the ligule f is the stamens. +T - Asclepias, the corolla opened (?); the ligule f is the stamens. +U - Asclepias, the corolla opened (?); the ligule f is the stamens. +V - Asclepias, the corolla opened (?); the ligule f is the stamens. +W - Asclepias, the corolla opened (?); the ligule f is the stamens. +X - Asclepias, the corolla opened (?); the ligule f is the stamens. +Y - Asclepias, the corolla opened (?); the ligule f is the stamens. +Z - Asclepias, the corolla opened (?); the ligule f is the stamens. +AA - Asclepias, the corolla opened (?); the ligule f is suppressed (thinned). +BB - Asclepias, a diagram showing how to open up a flower to see its parts. +CC - Asclepias, a diagram showing how to open up a flower to see its parts. +DD - Asclepias, a diagram showing how to open up a flower to see its parts. +EE - Asclepias, a diagram showing how to open up a flower to see its parts. +FF - Asclepias, a diagram showing how to open up a flower to see its parts. +GG - Asclepias, a diagram showing how to open up a flower to see its parts. +HH - Asclepias, a diagram showing how to open up a flower to see its parts. +II - Asclepias, a diagram showing how to open up a flower to see its parts. +JJ - Asclepias, a diagram showing how to open up a flower to see its parts. +KK - Asclepias, a diagram showing how to open up a flower to see its parts. +LL - Asclepias, a diagram showing how to open up a flower to see its parts. +MM - Asclepias, a diagram showing how to open up a flower to see its parts. +NN - Asclepias, a diagram showing how to open up a flower to see its parts. +OO - Asclepias, a diagram showing how to open up a flower to see its parts. +PP - Asclepias, a diagram showing how to open up a flower to see its parts. +QQ - Asclepias, a diagram showing how to open up a flower to see its parts. +RR - Asclepias, a diagram showing how to open up a flower to see its parts. +SS - Asclepias, a diagram showing how to open up a flower to see its parts. +TT - Asclepias, a diagram showing how to open up a flower to see its parts. +UU - Asclepias, a diagram showing how to open up a flower to see its parts. +VV - Asclepias, a diagram showing how to open up a flower to see its parts. +WW - Asclepias, a diagram showing how to open up a flower to see its parts. +XX - Asclepias, a diagram showing how to open up a flower to see its parts. +YY - Asclepias, a diagram showing how to open up a flower to see its parts. +ZZ - Asclepias, a diagram showing how to open up a flower to see its parts. + +Cross-pollination is most commonly effected by insects (especially bees), +flies and beetles. In some cases it may be effected by birds (e.g., Eriophorum +drumon (Achillea vulgaris), Bursaria spinosa), others are heterostylous (long- and short- +styled: *Pentameris officinalis*), or they are protected against rain, +and excludes certain insects. Some are barren when self-pollinated (*Pentameris*) + +20COTYLEDONES. + +**NUCULIFER.** + +535 + +*officinalis*, *Echinus *vulgaris*; others which have but little honey, may, failing insect-pollination, fertilise themselves, and in *Myrcium excelsior* this regularly occurs, so that the authors are brought into contact with the stigma. Honey is secured on the flowers of *Echinus* by the Albatross, and is especially in the northern temperate zone. Its flavour is very agreeable, and its pleasant officinale, in the root of *Symphoricarpos*; red dyes are found in some roots (e.g. *Albant-root*, the root of *Albantia*); and in the leaves of *Lonicera*. + +S. E. Europe, Asia Minor; some are *pulmonae*: *Cynoglossum*, *Echinus*, *Achillea*, etc. Several species are cultivated chiefly on account of their pleasant scent; essential oils are very rare. + +Other plants yielding a large quantity of honey are shrubs; a few are herbs or trees (Teak-Tree); some are lianas. The branches are often square; the leaves are simple, alternate, entire, and sometimes compound. This inflorescence is ra- + +A diagram showing the structure of a flower. + + +B diagram showing the structure of a flower. + + +C diagram showing the structure of a flower. + + +D diagram showing the structure of a flower. + + +E diagram showing the structure of a flower. + + +F diagram showing the structure of a flower. + + +G diagram showing the structure of a flower. + + +H diagram showing the structure of a flower. + + +I diagram showing the structure of a flower. + + +J diagram showing the structure of a flower. + + +K diagram showing the structure of a flower. + + +L diagram showing the structure of a flower. + + +M diagram showing the structure of a flower. + + +N diagram showing the structure of a flower. + + +O diagram showing the structure of a flower. + + +P diagram showing the structure of a flower. + + +rarely branched; five petals in a gamopetalous corolla, which is often tubular; but rarely such as an extens in as in the Labiate, and the upper lip in some is larger than the under, or even wanting altogether (e.g. *Cynoglossum*, *Echinus*); or 2-3-lobed (not grooved or divided), 1 or 2-lobed, or all in the Labiate, divided into four loculi with an erect ovule in each, but in some the anterior carpell is suppressed. The stamens are usually 4, but sometimes 2-6; filaments free or united with nut-like bristles; in *Ficus* (digitaceae) leaves a droop with a 4-loreal stome; in *Cladophora* a similar fruit, with four free stones; in *Lentaria* a bilobed stone, with two free stones; in *Lycium* (Solanaceae) one stone; in *Corydalis* small or absent—*Liparis*, *Stachys*, *Beechwood*, *Prunus*, *Cytisus*, *Collinsia*, etc., all with 4-lobed leaves; in *Ceratostigma* (Scrophulariaceae) one small or absent—*Liparis*, *Stachys*, *Beechwood*, *Prunus*, *Cytisus*, *Collinsia*, etc., all with 4-lobed leaves; in *Ceratostigma* (Scrophulariaceae) one small or absent—*Liparis*, *Stachys*, *Beechwood*, *Prunus*, *Cytisus*, *Collinsia*, etc., all with 4-lobed leaves; in *Ceratostigma* (Scrophulariaceae) one small or absent—*Liparis*, *Stachys*, *Beechwood*, *Prunus*, *Cytisus*, *Collinsia*, etc., all with 4-lobed leaves; in *Ceratostigma* (Scrophulariaceae) one small or absent—*Liparis*, *Stachys*, *Beechwood*, *Prunus*, *Cytisus*, *Collinsia*, etc., all with 4-lobed leaves; in *Ceratostigma* (Scrophulariaceae) one small or absent—*Liparis*, *Stachys*, *Beechwood*, *Prunus*, *Cytisus*, *Collinsia*, etc., all with 4-lobed leaves; in *Ceratostigma* (Scrophulariaceae) one small or absent—*Liparis*, *Stachys*, *Beechwood*, *Prunus*, *Cytisus*, *Collinsia*, etc., all with 4-lobed leaves; in *Ceratostigma* (Scrophulariaceae) one small or absent—*Liparis*, *Stachys*, *Beechwood*, *Prunus*, *Cytisus*, *Collinsia*, etc., all with 4-lobed leaves; in *Ceratostigma* (Scrophulariaceae) one small or absent—*Liparis*, *Stachys*, *Beechwood*, *Prunus*, *Cytisus*, *Collinsia*, etc., all with 4-lobed leaves; in *Ceratostigma* (Scrophulariaceae) one small or absent—*Liparis*, *Stachys*, *Beechwood*, *Prunus*, *Cytisus*, *Collinsia*. In the ovary not being 4-lobed with gymnospermous, but unifoliate, almost spherical or void with a terminal style. Again, the leaves are not so com- +780 pletely compound as those of the Tropeae, these are several in America, especially +*Lentania-speciosa*: shrubby weeds—Many of those mentioned are ORNAMENTAL +plants—such as: -the "Grape" (Vitis), -the "Holly" (Ilex aquifolium), -the "Pine" (Pinus), -the "Pineapple" (Ananas), etc., have strongly-seeded leaves; the Teak tree (*Tectona grandifolia*) is one of the largest trees in East India, and has a very hard wood. +In many cases there is no leaf at all—the "Tropical" (Dipterocarpus), on the tropical coast. +The endosperm emerges from the ovary, carrying the embryo with it; +the embryo ultimately buries itself in the endosperm. In this way many of the +species which have no leaves at all have their large, green cotyledons, which are borne on an almost hairy or rosetted stem. The seedling thus developed +has been called "the first plant". The "Tropical" has also been called "the first". One special cell of the enloumber as an earlier period becomes a highly-developed organ of nutrition, growing into a much-branched ac, very rich in protoplasm. + +536 +DICOTYLEDONES. + +Order 4. *Labiate.* The special characteristics are: the *sparse* stem, the *opposite leaves* (without stipules), the inflorescences which are formed by two double or three simple scrophulary cymes, the *infloral corolla*, the *distinct* stamens (the posterior stamen entirely suppressed) (Fig. 574), and the *4-partite* scrophium with *not-like* fructifera. The floral formula is 5S, P5, A5 (the posterior stamen is generally suppressed). + +They are chiefly aromatic plants (herbs, shrubs, e.g. Lavender, or trees), volatile oil being formed in internal cells or in the glandular hairs, which cover all green parts. The stem is always more or less markedly square; the leaves are borne upon the stem in opposite pairs; the flowers are produced by nearly any other characters. The inflorescences are double unipared scrophoid cymes, which may be situated at some distance from one another in the axis of the foliage-leaves (Fig. 575 b), but when they are close together, they are bract-like, they are crowded into spike-like inflorescences (Lavandula, Mentha, Salvia, etc.), each of these so-called *scrophoid cymes* (or *scrophoid rules*) being a double unipared scrophoid cyme (Fig. 574). (Solitary flowers are found in e.g. Scutellaria, and Origanum.) + +Fam. 574—Diagnosis of *Lamiaceae*. +574-Diagram of Lamiaceae. +
Fam. 574—Diagram of Lamiaceae.
+ + + + + + + + + + + + + + + +
A circular diagram with a central circle and four smaller circles around it.A circular diagram with a central circle and four smaller circles around it.A circular diagram with a central circle and four smaller circles around it.
838.839.840.
Figs. 588.—Diagram.Figs. 589.—Longitudinal section of flower.Figs. 590.—Longitudinal section of fruit (1).
+ +*Galium* (Gallium).—The flowers are small; they are 4-angled, and have a small 4-partite, rotule corolla; 4 stamens, and 2 free styles. The fructifera are un-lke. The inflorescence is a paniculate dichasium passing into helioide cymes.—*Asperula* (Woadroot) is distinguished from the above by its 5-angled or fusiform-shaped corolla; 1 style.—*Bubia* (Madder); *Asperula* (Woadroot) is almost always 5-angled; the corolla in *Galium*, but (most frequently) a 5-merous flower; and the fructifera are "drupean". *Sherardia* (Field Madder); the flowers are clustered in closely arranged umbels; the corolla is 4-angled; the petals are free; while the number of petals and stamens is 4. The corolla is funnel-shaped. +—*Valleriana*. *Crocus*. + +The stem-leaflets are, in some instances, promiscuous by hooked appendages on the fructifera (e.g. *Galium aparine*). + +The small flowers of the *Scilla* are frequently collected in compact inflorescences, and are therefore rendered more conspicuous; slight prominence is + +553 + +BUSHILIS + +found in some, self-pollination in the species which are less conspicuous. +Many species are heteroclitic. *Myracodon*, *Hydpephyrum*, and other genera +belonging to the same family, are self-pollinated by means of stigmatic papillae and +passages initiated by the necta. + +About 4,300 species; temperate or tropical species occupy the South Pole; especially +American. The American species are mostly trees.—Several are effective on ac- +count of the large amount of alcohols and glycerides which they contain. The most +important genus is *Cecropia* (Brazil), with its large leaves, *Cecropia peltata* (Brazil), +*C. microcarpa*, etc.) whose bark contains the well-known febrifuge and tonus, +*Quinine*, Cinchona, etc.; Quinine is also found in *Eucalyptus*, *Lindera*, etc. +The leaves of *Cecropia* contain a bitter principle, *cecropin* (Brazil). +Caffeine is official. The use of the seeds of the coffee plant ("the beans") was first known in Europe in 1688.—There are only a few which con- +tain caffeine, but many others contain a great deal of this valuable drug. The departs +adrents, the Woodruff, in which green coloring materials are also found. The root and root-stalks of *Rudis* nuttallii, the Madder (S. Eur. Orient., Fig.) +are used as a stimulant. The leaves of *Coffea* arabica contain a bitter principle, the +analine. Boden dye is also obtained from the roots of species of *Apocynum* +and *Aristolochia*. The leaves of *Coffea* arabica, obtained from +(Coffee) (S. E.A.), which is used in dying and tanning.—The order does not furnish any ornamental flowers. + +Order 2. **Caprifoliaceae**. This order agrees with the Rubiaceae in having opposite leaves and an epigynous flower, most frequently 5-merous with the ordinary tetraecary diagram, but in some species it is 7-merous or even more merous. The calyx is usually persistent, corolla 3–5, most frequenty 3 (not 2, which is the usual most number in the Rubeaceae). The fruit is generally a berry or a drupe, but the most important, and in any case most easily recogni- +zable, is the capsule. In some cases, where they are present, they are interpetiolar and are most +frequently small.—The majority of plants belonging to this order are shrubs or +trees. Composites have been included here because they belong to a few +genera: *Sassafras* and *Phytolacca*; in the common Elder (Sambucus nigra) +they are in some instances glandular and small, but in other cases larger +leaves occur; in *Elaeagnus* (Elaeagnaceae) they are glandular; in *Galea* (S. +chabri) they have the normal leaf-like form; in *Fischeria* often they are pre- +sent as narrow lobes at the base of the petiole; in others they are completely +absent; in *Hibiscus* they are present but not very conspicuous. The calyx, +as in the Stellaria and Agrostis, is often very insignificant. + +I. Lonicera. Honeysuckle Group. This has compoundal or tubular corolla which are often xygomorphic; in connection with +the length of the corolla the style is long, filaments, and most fre- +quently a large, capitose stigma. There are several ovules in the loculi of the ovary, and the fruit is most frequently a berry. + +A stylized illustration of a honeysuckle flower. + +554 +DIOTYLEDONES. + +*Lonicera* (Honeysuckle). Shrubs, sometimes twiners. The corolla in some species is considerably bilabiate (Fig. 501), with 4 lobes in the upper part, and 2 in the lower, but in others more regular, tubular, or campanulate. The flowers are borne in capitate inflorescences, which are compound and formed of closely compressed 3-flowered dichasia (sect. *Caprifolium*), or in dichasia with 2 flowers (the terminal flower is wanting). The ovaries and + +Fig. 501.—Lonicera. +fruits coalesce in some (sect. *Xyloleum*). The opposite leaves in some species unite with each other and form a broad collar encircling the stem (Fig. 501). Above this collar the leaves are sessile, or nearly so, in the leaf-axils.—*Dierama* (*Veratrum*); with a 2-lobed, 2-valved capsule.—*Symphorarum* (Snowberry) has an almost regular, funnel-shaped corolla; a peculiar feature is that the ovary is composed of two parts, one being an ovule in 3 rows, all of which are short; the 2 lateral ones, on the other hand, each have only 1 ovule which is developed. Different forms of leaves are frequently found on the same branch; they are entire or lobed. + +1 + +**Sambucus**, Elder Group (Fig. 502). This has a *rotate*, *regular* corolla, extrorse anthers, a very short and thick (or almost absent) style, with tripartite stigma, and only 1 pendulous ovule in each of the loculi of the ovary. The fruit is a "drupe" with 3-(-5) stones. The inflorescence is made up of cymes grouped in an umbel-like arrangement. + +*Sambucus* (Ehler, Fig. 502) has imperfective leaves and a "drupelike" fruit. The corolla is regular, the petals are opposite on the apex of the fruit. It is a species with black fruits, but some species have red fruit; *S. alba* is perennial herb; the others are woody. *Viburnum* (Guthrie & Hemsley) has simple leaves (pinnate or palmi- +nate), and a fruit which is a "drupe", with 2 or 3 loculi, which is compressed, cartilaginous, and parchment-like; 2 of the loculi of the ovary are aborted. (*In* F. *epica* the marginal flowers of the inflorescence are barren, and in that case these corollae are generally sterile; hence the cultivated Viburnums have only barren flowers, with large corollae.) + + +A: A close-up view of a flower showing the stamens and pistil. +B: A diagrammatic representation of the flower structure. +C: A diagrammatic representation of the flower structure. +D: A diagrammatic representation of the flower structure. +E: A diagrammatic representation of the flower structure. +F: A diagrammatic representation of the flower structure. + + +Fig. 502.—Sambucus nigra: a. corolla; b. style; c. ovule. + +**Lonicera** (Lindley) corolla (the only species) is an extreme form of the order; it has a 3-lobed corolla, with 3 stamens, and a single carpel with 3 loculi which are not developed into ovaries. The fruit is a nut, which is enclosed by the two large bracteoles, which are covered by sticky, glandular hairs, and serve as a means of protection to the seed. + +(*Adoxa*, which was formerly classed in this order, appears, according to recent investigations, to be more properly placed among the Saxifragaceae.) + +In *Lonicera* (Fig. 503) the corolla is regular; the petals are opposite; they are rendered conspicuous by being arranged in closely-packed inflorescences; they are matted together and form large surfaces, and in the last mentioned genus there are also many glands on the calyx and sepals, large rays, +flowers, which are of service in this respect. Honey is secreted in the nectaries at the base of the styles. In the genera with rotule flowers, as Viburnum and + +556 +**DICYCTOLOXON** + +other Sambucus, the honey lies so exposed and in such a thin layer, that only flies and insects with short proboscis can procure it; but, however, until time flowers lie on the ground, and the bees are numerous, the honey is not self-pollination frequently takes place. The flowers of the Caprifoliaceae, which, with the exception of the Honeysuckle, are very small and light-flying insects with long proboscis, open in the evening, and at this time they are off the strongest scent. + +Dicyctoloxon, 330 species; especially outside the tropics in the Northern hemisphere. In this country they are found especially in bulges and as under-shrub--ORIENTAL--the Flowers and fresh fruits of the Elder (C. nigra), the fruits of the Blackberry (Rubus fruticosus) are often eaten by man. + +**Genus 34.** **Diphasaceae.** + +The leaves are opposite and without stipules. The flower (Figs. 503, 505, 508, 509, 600) is epigynous, zygomorphic or asymmetrical. 5-merous with S, P5, stamens typically 5, but by suppression never more than 4; sepals and petals carpels usually 5 or less in number and almost symmetrical in the extreme forms. The ovary has 3-1 locali, but only one locali has an ovule, which is pendulous with the micropyle turned upwards (Fig. 504). A fruit -embryo straight, with the radicle pointing upwards (Fig. 507), without a testa. + +The inflorescences are distinct dichasia in Valerianaceae, but in Diphasaceae and Calyceraceae they are crowded together into capitula. + +This family is closely allied to the Berbaceae through the Valerianaceae, which have almost no flowers and are similar to the Caprifoliaceae. It is within the highest development in the Diphasaceae, which are compound plants but differ from Compositae in the position of the ovule, etc. + +Order 1. **Valerianaceae.** Herbaceous plants or under-shrub with opposite leaves, often pinate; stipules absent. The flowers are epigynous and zygomorphic or asymmetrical; sepals and petals are entirely without any plane of symmetry (Fig. 503). The calyx and corolla are 5-merous, but the calyx is frequently very insignificant and ultimately a papilla, as in Compositae; the corolla is rarely divided into a spatula at the base. Most frequently, only 3 (-4) of these are lobed; these are free. Carpels 3, which form an inferior ovary, often with 3 locali; but only 1 of the locali contains 1 pendulum; antrorseous ovule (Figs. 503, 504 d); the other locali are empty + +A diagram showing a flower of Valerianaceae. + +**DIPRACALES.** +557 + +and shrink up more or less completely. (Compare Fig. 203 A, B). Style 1, stigma tripartite. Endosperm absent; embryo straight, with the radicle directed upwards. + +The inflorescences are dichasia, or unipared scapular cymus with the branches developed in the axil of the second bractlets. Both the bractlets are generally small, but in *Patrinia* they are large and conspicuous. The flowers on the branches of the inflorescence—5 stamens do not occur (except perhaps in *Patrinia*). The suppression of stamens and carpels takes place most readily on the first bractlet, which is usually larger than the second. On the first bractlet (a) (Fig. 203), though its branch is suppressed in the dichasium; after that the pos- terior median stamen is next suppressed. + +By the suppression of the stamens and carpels by the inflorescence and the flower, the order is reversed in the suppression of the gynoecium and especially to the Samoanese. + +In the least modified (oldest) forms, *Patrinia* and Nardostachys, there is an almost regular flower, a 5-cornic calyx, 4 stamens, and 3 bulbous ovary, all of which however are barren. The stamens in *Valerianaefolia* are reduced to 3, in *Fedra* to 2 (posterior), and the calyx is reduced to 2 lobes; the 2 empty liliops in the ovary are still visible. Fedra has a small spur at the base of the corolla. *Valerianaefolia* has a tubular calyx-like calyx (pappus), an unnamet- ral, salver-shaped corolla with a sac-like, meconiferous spur at the base; the ovary is a simple cup-like one in the ovary (Figs. 504, 505). + +*Centranthus* (Fig. 203) is still further reduced. The corolla has a spur and only 1 stamen; unpaired scapular cymus with 4 rows of branches. In the last two genera there is a single flower on each branch; this is divided internally into two compartments (inheated by a dotted line in Fig. 203), one of which encloses the style. This style is low in *Fedra*, but in *Centranthus* it reaches as far as the base of the corolla. The calyx is tubular and rolled up before the ripening of the fruit. 12–20 in number (Fig. 204 A, B). Fedra has a long spur at the base of the corolla; this spur projects from the centre of the flower (Fig. 205 a), the stigma in the second (b) when the stamens have become bent backwards. (*F.* dioicae is diclicous.) + +A diagram of Federa quintula. A Diagram of Centranthus. +A diagram of Federa quintula. A Diagram of Centranthus. + +558 + +DISOTLEDONES. + +with large $g.$ and small $q.$-flower; especially from the temperate and colder parts of the northern hemisphere of the Old World, Western North America and the South American continent, such as the volatile oil of Valerian; their other similarity in the + +A. Fig. 896.—Valeriana: A corya (longitudinal section). B. False fruit. +B. Fig. 898.—Valeriana: A flower section at the $d$ stage; b in the $q$. thilanthum. +Dyssacus; the rhizome of *V. officinalis*. —The true Indian "Nardus" is a species of *Nardostachys* and is sometimes used as nard. +Nardostachys (Himalaya). A variety of *Paeonia lactiflora* albitiora is sometimes used as nard. + +Order 2. Diapacaceae (Tessela). Herbs with opposite leaves without stipules. The flowers are situated in compact capitula each with an involucre. A characteristic feature of the order is that each flower of the capitulum has a gamophyllous "epicalyx". + +C. Fig. 897.—Corydalis rubra. Forster: A corya and spur in longitudinal section. (Mag.) +D. Fig. 899.—Sesbania stenopetraea. Fruitinum- +tum: A fruit with a long pedicel. The fruit may be seen as the fruit drawn out into a beak, with +swollen embryo and radicle directed upwards. + +DIAPYCALES. +559 + +(Figs. 507, 509, 609), which envelopes the inferior ovary. The flowers (Figs. 509, 510) are 3-5-nerved (53, P5), stamens typically 5, (G1), but the calyx often expands at the edge into a membrane with 5, or an indefinite number of bristles or teeth (pappus. Figs. 507, 600), and the zygomorphic, funnel-shaped corolla is usually divided into two lobes, the upper one being frequently 4-partite (Fig. 509), the two lobes of the upper lip coalescing into one lobe, as in certain Labiate, Veronicas and Plantago; the aestivation is indurate. + + +A diagram showing the structure of a flower with a four-lobed corolla. + + +Fig. 508.—Induration of the corolla-lip (the same as in fig. 609). +Fig. 509.—Induration of the corolla-lip (the same as in fig. 609). + +The stamens are never more than 4, the posterior one remaining undrooped; they usually have free anthers which generally project considerably (Fig. 509). The filaments are united with 1 pen- +dulous anther. There is 1 meridional apical leaf; fruit a nut-like seed, containing endosperm and with the radicle turned upwards (Fig. 507). + +The flowers do not always open in centripetal order, a fact which may be observed especially in the Diapycaceae, in which a zone of flowers round the centre opens first, and then those on the periphery open successively both inwards and outwards (Fig. 509). This has probably some connection with the fact that the capitulum has arisen from the confluence of several dichotomous inflorescences, each of which had its own axis, and opened towards the circumference, or in a zone at the centre.—The morphological explanation of the W.B. + +60 + +560 + +**DIOTYLEDONES.** + +"epiclypeus" is not quite certain; in all probability it is formed from two united bracteoles, for an "epicyclpeus" is distinctly formed in this way in one of the Valerianaceae, *Papaveraceae.* The top-flower is larger and more irregular, labiate or ligulate, than the disc-flower, yet not so high as a genus as in the Compositae. + +A. A scariosum bract to each flower. *Scariosum* has a 5-lobed corolla; the "epicyclpeus" has a dry, scariosum, often finally large corolla; and the "epicyclpeus" is usually surrounded by several bracteoles (generally 5) (Fig. 507). *Succacia* *gigantea* (Leveritii-vitii) has a corolla with 5 lobes; the collar of the "epicyclpeus" is herbaceous; the calyx as in the preceding. *Pterocaulon* *Diplocarpos* (Tessel); large, spiny and stiff-haired herba with capitula, or short, thick spikes on which both the involucres and the flowers are covered with long, soft, stiff and spinose (Fig. 508). The "epicyclpeus" has short teeth, or is almost entire. The leaves of the stem unite together in pairs, so that shallow cup-like spaces are left between them. *Cephalaria* - *Morina* : the flowers are falsely verticillate as in the Labiatae; the calyx has a laterally-placed, entire, or emarginate lobule; or stamens, or 3 large and 2 small ones. + +B. Disciferae, but no true bract to each flower. *Knautia*, the corolla is 4-partite, the calyx cup-like, with many bristles or teeth on the edge. + +Pollination is in many species effected by insects. The honey is secreted by a ring round the base of the style. The flowers in our native species are commonly white or yellowish-white; but they are often blue or purple, especially in the Mediterranean and the Oriental ; the order is not represented in the South End Islands, Australia and America.—The heads of the true Tussel (Tussilago), *Helenium*, *Centaurea*, etc., are composed of numerous flowers, which are hooked at the point. The order has bitter properties; tannin, etc.; but no species are used in medicine or the homeopathic. *Scabiosa atriplicifolia*, etc., are included in this Order. + +Order 3. Calyceraceae. This order resembles the Compositae in the valuate estivation of the corolla and the more or less united stamens, and the Diplocarpos is like it in having a false verticillate corolla. The calyx is frequently composed of 5 distinct scales. As "epicyclpeus" is lacking—20 species; America. + +Family 35. Campanuline. + +The flower is epigynous, perfect, with 5 sepals, 5 petals, and 5 stamens; but sometimes wanting one or two of these parts. The sepals in all cases are distinct, but narrow and pointed, so that the estivation is open. The corolla is gamopetalous with (as in the Compositae) calyceate, or slightly infolded-calvate estivation. The + +CAMPAULINE. +501 + +stamens are nearly always situated on the corolla without being united to the corolla (Fig. 601, 604). The anthers adhere or unite and form a tube with interior anthers from which the pollen is swept out by the projecting, brush-like hairs on the style (as in the Campanulaceae), or by a long, slender, hair-like anther in each lobe. The fruit is generally a many-seeded capsule (or berry). Embryo in the centre of a feathery endosperm—The majority are herbs with scattered leaves, without stipules. The presence of stamens and tendrils, together with the tubular formation of the anthers, the pollination, etc., indicate a relationship with the Composite. + +The Cucurbitaceae are by some authorities placed in this family as being most closely related to the Campanulaceae. Although the corolla is most fre- +quently represented by a tube, yet it is often wanting. The stamens are present, yet at account of the structure of the corolla, and for other reasons, the Cucur- +bitaceae are not included in this family. The flowers are almost double +proceed upwards to the calyx, with which, in addition to the appearance +of indusium and lateral sepals (Glossose), there are many corresponding +features. The fruit is a berry or capsule. The presence of a tubular for- +mation of the corolla, tendency of the anthers to adhere or unite, probably +with a style-brush, etc.). The inflorescence of Jasion is almost identical with that of the Campanulaceae. + +Order 1. Campanulaceae (Campanulae). The flowers are regular and in some only semi-epigynous, 5-meres, except in the gynoecium which is 3-meres (the unpaired, median carpel being generally posterior), more rarely 2–3-meres, and has a corre- +sponding number of stigmas and loculi in the ovary; the placen- +tion is axile; the perianth is usually persistent; the ovary is superior; +the sepals are free; the stamens frequently have broad, free bases (Fig. +601 H) which cover the nectariferous upper surface of the ovary; the anthers only fit loosely together, and become separated as soon as they are detached from their filaments; the style is +studded by sweeping-hairs (stylar-brush), which ultimately be- +come invaginated; the stigmas do not unfold until the stamens have shed the pollen (Fig. 601 E, G). Fruit a capsule.—Herbs, +more rarely shrubs or trees. Leaves alternate or opposite, and incised, +undivided leaves without stipules. The inflorescence is most fre- +quently a raceme or spike with terminal flower. + +A. Capsule opening at the base by pores and with all valves, +Campanula (Campanula) has one or two short, strap-shaped, rarely +almost rotund; capsule oblongous. The pores of the capsules are found near +the top of the fruit when it is erect, and near the base when it is pendu- + +502 +DIOPHYTEDODEXEL. + +lous, so that the seeds are not liberated unless the capsule is forcibly shaken, and they are thus ejected to a considerable distance. — Phylocarum (Ram- +pan) has free persistent sepals, which are reflexed at the apex and form a tube, and bear the stamens (Fig. 601); inflorescence compound, spike-like or capitate, in the latter case resembling that of the Composite, and frequently with an involucre similar to the one presented by the Compositae. — Phyllocladus (flower-branch), synanthic capsule; *Mikania* (flower-branch). — Sympandrus has synanthic anthers. +B. Capsule with valves at the apex, loculicidal dehiscence; *Jasione*; the petals are almost free. The anthers are united at the base (syngynous). The flowers are situated in capitate umbels with involucres.— *Wahlenbergia* ; *Filodendron*. + +A +B +C +D +E +F +G +H + +Fig. 601.—Phylocarum. Flowers and parts of flowers in various stages of development. + +C. Berry: *Carminaria*, flower-branch; leaves opposite. Proximally in general (Fig. 601). 510 species; principally in temperate countries. Several genera furnish ornamental plants, but few of little use for other purposes than ornamentation. The *Phytolacca*-species are large and may serve as pot-bushes (*C. sessilifolia*, *F. piscator*). + +Order 2. Cyphaceae. In this order the corolla is syngynous and the stamens free; the calyx is intermediate between orders 1 and 5—about 24 species; Africa. + +Order 3. Lobeliaceae (Lobelian). This order may briefly be described as Campanulaceae with syngynous flowers and anthers united into a tube, in most cases slightly bent; generally 2 carpels and an inserted position of the flower, i.e. the median sepal is + +9/22 + +CANPAULINACEAE. 563 + +tinned anteriorly (Fig. 602) (a position which is found to occur within the Canpaulinaceae). A twisting of the petalme takes place even before flowering (as in the Orchids) so that the ordin- +ary position of the 5-merous Dictyolodums appears to be restored. +The symmetry of the flower is especially present in the corolla, +which is usually regular, but irregular in some species, as shown in +Lobelia, anteriorly (apparently posteriorly) deeply cleft (Fig. 602). +There is 1 style, but the stigma is capitulate and sur- +rounded at its base by a whorl of leers, which assists in pollination +as in the Orchids. The stamens are 5, inserted on the corolla +in the Canpaulinaceae and Composite. There is no terminal flower in the spinate, or racemose inflorescences.—Lobelia has a capula, several +others have berries. *Tintina* (regular flower), *Heterocodon* has a spur; + +Fig. 602.—Diarrhena of Lobelia floridana. +Fig. 603.—Lobelia floridana. +Fig. 604.—Flower (3). + +Siphocampylus: *Lepidium* (pyriadium), *Climonia* (conular fruit), *Melitria* +(all the petals are free). + +Eustomoniiis and Prostratums. About 500 species, especially in the +Tropics and Subtropics, are grown as ornamentals, and culti- +vated in gardens and conservatories as ornamental plants (*Lobelia bicolor, +crispa, falconia, etc., Siphocampylus, Centropogon*). The latter of several species of *Lopezia* are used as ornamentals under the name "Lobelia" (the albatross): + +Order 4. *Gardeniaiaceae.* Chiefly Australian (200 species), closely related to +Orders 3 and 5, but without inner. The style is provided with a "collecting- +cup" which receives the pollen before the flower opens; it has a small, hairy +spur through which the pollen passes into the tube of the flower, +which may remain when the pollen is shed; it is sensitive and exhibits move- + +Order 5. *Gardeniaiaceae.* Chiefly Australian (200 species), closely related to +Orders 3 and 5, but without inner. The style is provided with a "collecting- +cup" which receives the pollen before the flower opens; it has a small, hairy +spur through which the pollen passes into the tube of the flower, +which may remain when the pollen is shed; it is sensitive and exhibits move- + +564 +DIOTYTOLEONES. + +ments when touched.—Herbs, under-shrubs, less frequently shrubs. *Genista*, *Lechenaultia*, *Sorenia*. + +Order 3. *Diplocarpaceae* (or *Candollesaceae*): 100 species, the majority Australian; symmorphous flowers, but with the ordinary position. The anterior petal is very small. The chief characteristic feature is the presence of only 2 distinct stamens, one of which is usually much larger than the other; the upper is regular-column; this is bent like a knave and sensitive at the bend to such a degree that when touched it jerks violently across the flower to the opposite side and then loses its sensibility.—Herbs, less frequently male-sterile. +**Glycine** (Candolles). + +Family 30. **Aggregates**. + +The flowers, which are borne in "capitula" (Figs. 605, 610), are epigynous (Fig. 605 C, D). *Sesamum*—seeds in the calyx corolla and antherium, the latter opening by a tube with 2 corolla (SA, PS, A5, G2). The anthers are united into a tube (syngeneous) (except *Amandraeum*) which surrounds the boid style. There is never more than 1 corolla in the ovary, and antherium, an antropous ovule. The stigma is sessile on a stalk with the antherium; the calyx generally persists as a tuft of hairs (pappus) (Fig. 606) on the summit of the fruit. Embryo without endogynia; the radicle directed downwards. +Only 1 order known. + +With respect to the inflorescence and the development of the individual flowers, there is a very close resemblance to the Dipna- +ceae, which stand on the same plane of progression as the Convolvulaceae. In both families there is no difference in the last stage in the process of evolution, the Dipnaceae form the final stage of the Rubiaceae-Dipnaceae. + +Order Composite. (For the principal characteristics com- +pare those of *Rubiaceae*. The composite are chiefly herbs, +but trees and shrubs also occur in tropical countries. The leaves may be scattered or opposite, but have no stipules. The outer leaves of the *aculeus* as a rule are barren, especially when numerous; but in some genera they are almost equal to the ray-flowers of the capitulum; in a few instances all leaves fertile (e.g., *Tropaeolum*, *Tupaeus*). The capitula are many-flowered, with the exception, e.g., of *Echinacea*, which has 1-flowered capitula (see page 378). The receptacle is often conical or cup-shaped, fre- +quently conyrous with centrilocal order of development. The form of the receptacle is an important character for the division of the genera (flat, convex, conical), and also the presence of scales; + +A diagram showing a composite flower head. + +AGGREGATE. 563 + +these may be one scale (bract) for each flower (Fig. 610 br.), or a large number of bristles, which do not each correspond to a leaf, or the receptacle may be entirely without covering (naked). The flowers in open capitula are usually perfect, but those in dense capitula may be of the same sex, and their form and colour are in that case the same, or the sexes may be different, in which case the form and colour are also most frequently different : the ray-flowers have projecting labiate or ligulate corollas, while the disc-flowers have tubular corollas. As a rule in the latter case the $z$-flowers are at the circumference, and the $q$ in the centre, less frequently $q$-flowers at the edge and $q$-flowers in the centre. The ray-flowers in some genera are nester (e.g. Centaurea). Some are dioecious. + +There is no trace of an epicalyx (in contrast to the Dipsacaceae, which they generally so resemble). The formation of the calyx is very varied. The calyx always consists of a very small cushion-like structure, most frequently developed later than the corolla; the 5 corners, which correspond to the 5 sepals, in a few + +A diagram showing a capitulum with rays and disc florets. +610 + +Fig. 610.—Centaurea arenaria: A capitulum; B expanse in longitudinal section; C flower of capitulum; D ray-flower; E disc-flower; F stamens. The rays are at the circumference, and the $q$ in the centre, less frequently $q$-flowers at the edge and $q$-flowers in the centre. The ray-flowers in some genera are nester (e.g. Centaurea). Some are dioecious. + +There is no trace of an epicalyx (in contrast to the Dipsacaceae, which they generally so resemble). The formation of the calyx is very varied. The calyx always consists of a very small cushion-like structure, most frequently developed later than the corolla; the 5 corners, which correspond to the 5 sepals, in a few + +566 + +SOTTLEDEONE. + +instances are raised as 5 large, flat, membranous bodies, e.g. in species of *Xeranthemum*, *Catananche*, *Sphagnum*, etc.; in other instances, the calyx is raised into 5 points, which are often more or less apex, followed by others in rather uncertain numbers and with but slight indications of order, on the edge and on the outer side of the calyx between the 5 points; in other instances, again, the calyx is raised into 5 points, which are regularly arranged in order or definite number (Fig. 606 a, b); finally instances occur in which the edge is raised as a membranous collar, irregularly toothed and notched, or divided into small scales. There are naturally differences in the means of distribution corresponding to + +A diagram showing the structure of a flower with five petals. + +the differences in structure of the calyx. The fruitleaves a and b represent in their mode of distribution those of the wind, those like c, on the other hand, by attaching themselves to animals and human beings. The rays of the pappus are termed rachis when special cells project a little beyond the surface, but if these grow out, they are hair-like, forming a kind of bristle. In some cases the pappus is raised upon a long stalk, which is developed from the upper part of the fruit, and termed a beak (Fig. 606 a). The pappus does not attain its full development till the ripening of the fruit, i.e. until it is about to be of use. + +The corolla has various forms: (a) *radial* (Fig. 605 D), with a + +AGGREGATE. 567 + +shorter or longer tube, not always of the same bore throughout and especially slightly widened at the top to form a bell-shaped opening, with 3 regular teeth: (b) labiate after 4, i.e. with 2 petals in the upper half of the corolla, lower lip: (c) ligulate, i.e. the corolla persistent for a considerable distance on the interior side (as in the Labiate genus *Truncocaryum*) and prolonged into a long, strap-like portion (Fig. 609 A), which projects upwards. A distinction must, however, be drawn between the two types of false bignate corolla, viz. that in which the corolla has 5 teeth at the base (Fig. 609 A) and is made up of all the petals of the corolla united together; this is the usual condition in the *Ligulaceae*—floriferous; in the latter case (Fig. 609 D) the corolla is divided into 4 teeth (or is merely a double capitate corolla), and is only formed by 3 petals; the corolla is then truly bilabiate, the tongue is the large under lip, and the upper lip is very slightly developed, or even at a early stage quite suppressed. This false "ligulate" corolla is found amongst many plants, but it is not common among plants quite plainly, e.g. in *Tugeta*, especially in the double capitula. The venation of the corolla is peculiar; there are always commanous veins which run from the base of the tube to its mouth, and these veins end near a branch into the edge of the two nearest teeth. The mântle is frequently absent, but may be present, and then it has sometimes no connection with the other parts of the corolla. + +The *stamens* are attached to the corolla, and have free filaments (*Siphonium* has uniform filaments), but the anthers, which at first are free, adhere together and form a tube (Fig. 605 E): only *Astragalus* has free anthers; *Corydalis* is generally prostrate, and protrudes below the anthers as a thin, brown membrane of various forms (Fig. 605 E); appendages of various kinds are also found at the base of the anthers. The anthers open introrsely, out at the top of the tube by upward growth of their filaments; they are called "stylar-brushes" (Figs. 607, 608, 609); the filaments are sometimes sensitive (e.g. in the Corn-flower, Fig. 607), and shorten when touched; in *Corydalis* the tube is pulled downwards, and the pollen swept out at the top (Figs. 607, 608 A, B). + +A diagram showing a stylar-brush. +4 +B +D +E + +568 + +**DICOTYLEDONS.** + +The **style** divides at the apex into two branches (Figs. 609, 610), both of which generally bear on the inner surface two lines of + +A diagram showing the structure of a flower with the style divided into two branches. + +**Fig. 609.—Gomphrena arvensis : A, the upper portion of a flower; B, the lower portion of the same; C, a lateral view of the style with stylar-brush (b), stigma (b'), and stigmatic papillae (a). + +**Fig. 610.—Lobelia ensifolia : A, the upper portion of a flower; B, the lower portion of the same; C, a lateral view of the style with stylar-brush (b), stigma (b'), and stigmatic papillae (a). + +stigmatic papillae (Fig. 610 B, C) and being in shape, etc., very varied, are therefore employed as systematic characters—the most important being that they are usually long and slender, semi-cylindrical, long, and with long hairs, and finally bend backwards; the stylar branch bears slightly projecting stigmatic papillae on the inner side. + +**Fig. 606.—Achillea multifida.** + +This form is characteristic of the *Cichorieae* (Fig. 609 A, B). The style is uniformly cylindrical ; the branches are long, cylindrical or club-like, short, + +8 + +AGGREGATE. 569 + +not rolled back, with fine hairs externally; the stigmatic lines do not reach beyond the centre, and do not meet together. Characteristic of Erythrostemum, *Ferulina* (Fig. 603), *Cynara* (Fig. 604), *Carduus* (Fig. 605). The involucres in the form of a kouk, or very hairy (Fig. 600 C); the stigmatic line reaches as far as the apex of the bractlets and then converges; sometimes the stigmatic bractlets are united at their base, and sometimes they are separate (Fig. 600 D). The styrax branches are lanceolate, or linear, pointed; externally flat and trifoliate covered with hairs in the upper portion; the stigmatic lines occur where the bractlets are united at their base (Fig. 600 A, B). *Lobularia*, *Lobelia*, *Lunaria*, *Dahia*, etc. E. The stylos branches are linear, with long, brush-like hairs at their base, and with a short, conical appendage (Fig. 600 E). The stigmatic lines are broad, reaching as far as the bractlets' hairs, and do not meet together (Fig. 600 E). + +Characteristic of *Senecio*, *Helianthus*, *Helianthemum*, *Crepis*, etc. + +A ring-like mentary is found round the base of the stylo. + +The thin-walled cypselae (Fig. 600 C), with seeds fitting closely to the pericarp, have many different forms (smooth, ribbed, spinule, etc.). In some cases they are smooth and rounded, but sometimes it is drawn obliquely up the side (Controversa, etc.). + +The calyx, persistent on the apex of the fruit, has been described above. Some genera have two or three different forms of fruits in each species; others have only one form of fruit which is tubular reduced downwards, and without endocarp, but is rich in oil. + +The variously flowered capitula, whose normal tubular disc-flowers have been changed to ligulate flowers, may be termed 'dichotomous capitula'. + +The relationship of the Compositae to the Campanulaceae has been described above (page 561). The alliance with the Dipsacaceae is more apparent than real; for while the former have a pericarp and a final stage in other lines of descent, as in Arctiaceae among the Umbelliferae. + +I. CYNARES. Thistle Group. Flowers all $r$ regular, with tubular corolla. The receptacle is covered with numerous bracts, which cover the whole of the surface of the receptacle or the edges of the grooves in which these are placed have a well-marked fringe. The involucral leaves are numerous, imbricate, and are either prolonged into a flora or terminate with a involucral edge (Fig. 600 A). The involucral bracts are linear (Fig. 600 C). Nearly all have a hairy or feathery pappus. The filaments are sensitive. + +*Carduus* (Thistle); capituli ovate; involucral leaves compact, imbricate; with thorny points; the pappus-ovata are hair-like and united at the base by a ring (i.e. the calyx) and fall off together. +—*Cirsium* (Fig. 605) has a feather pappus, in other respects it is like Carduus. *C. arvense* reproduces and passes the winter by means of + +570 +**BICYCLIDEAE.** + +**Cynara** (Artichoke) has a fleshy pappus and large, solitary capitulum with broad involucral leaves; these have a flexuous base, and are usually 3-5-nerved. *C. cardunculus* (Cardunculus), *C. maroccana* (Mulch-thistle), its leaves with numerous white spots, *Onopordum* (Cotton-thistle). *Calcea* (C. benedicta) has a large, many-spined thorn on the receptacle, and a pappus of white scales. *Lepage* (Barbuck) is very similar to the above, but the receptacle is smooth, and the distribution of the fruit; in this respect it differs from the other inflorescences, and also in the fact that the pappus is short, and quickly falls off. The number of flowers per capitulum of *Carduus* (The common wild lettuce) is variable, from one to three; the bracts are linear, and the spines on the receptacle straightening out or bent backward; the internal ones are dry, and may be absent; the outer ones are long, and bear several bristles on the receptacle and edge of the corolla they are deeply cleft and lobed. +—*Centaurea* (Knapweed, Fig. 607). The ray-flowers are neuter, and generally larger than the disc-flowers; the involucral leaves are regularly arranged in two series, the outer ones being leaf-like with a dry, clary, often lobed, fringed appendage. The attachment of the fruit is lateral. *Serratula* (Swart-wort)—*Carthamus*, is characterized by having a single flower in each capitulum, but many such capitula are collected into a spherical head, which at the base may also have a few involucral leaves. The individual capitula have narrow, linear involucral leaves. There are about 100 species of *Centaurea* with 1-flowered capitula, all from warm countries. *Astragalus*, *Lunaria*, *Lunaria*, *Succisa*, etc. + +**3. Mutiniae. Lactiflora-Group.** Tropaeol (8). American forms whose rays are yellow or white, but blue in color. The involucres nearly the same as in the Thuidae. + +**3. Cichorieae, Choricic Group (or LILIIFLORE).** The flowers are all 5-petalled and have a ligulate, 5-merous corolla. The stamens branch out and are thin and prolonged (Fig. 600 B). Lactiflorous corollae occur in the majority (in this feature they resemble the Lobeliaceae and Campanulaceae). + +A. The pappus is wanting, or it is scale-like, but not long and hairy.—*Chlorisichorium*: capitula with blue flowers, borne singly or in small groups; the corolla is ligulate; there are 2-4 involucral leaves, an outer one of short and radiating, an inner of more numerous, longer and erect leaves; pappus, scale-like.—*Lupina* (Nipplewort). The few involucral leaves are nearly of the semeate, and persist forming a sort of casule round the + +AGGREGATE. 571 + +fruits, which are entirely without a pappus. There are only a few flowers in the small capitulum—*Arcturus* (Swain's *suncory*), *Catanaceae*, etc. + +B. The pappus is long and hairy (not branched), generally fine and silky-white. There are no scales on the receptacle. The two genera first considered have basal fruits.—*Taraxacum* (Dan- +delion) (Fig. 60 a); the capitula are many-flowered, and borne singly on the top of a leafless, hollow stalk—*Lactucea* (Lettuce) hortensis, *Lactucea* (Lettuce) sativa, *Crepis* (Hawksweed)—*Haworthia* (Hawk-wood) has many imbricule involucral leaves, and a stiff, brittle, bristly pappus—*Souchetia* (Snow-thistle); the capitula, when a little old, have a broad base, and are almost sessile in the form of a jug; involucral leaves imbricate; the fruit is a nutlet without a beak, rugated. The soft, white pappus falls off collectively. + +C. The pappus is feathery and branched; no scales on the recept- +acle; the capitula are solitary or in one whorl. The fruit has a long beak; the raya of the pappus are interwoven in the form of an umbrella.—*Sooreseu* has fruits like the preceding, but almost without any beak; involucral leaves many, imbricate.—*Zoolema* (Hawkbit) has a slightly feathery pappus. + +D. Long, shaft-like, deciduous scales on the receptacle; pappus feather-hygrophytes (*Cat's-ear*). + +**E. Eupatoriate**, Hemp-agropyron Group. All the flowers are free from each other; tubular and regular; the in- +volucral leaves are stiff and spiny; the receptacle is not covered with stiff bristles. The starry bracts are long, club- +like, or gradually tapering. There is no swelling below the stigmatic axis. + +Empetrorum (Hemp-agropyron): all the flowers are $\varnothing$—*Petastera* (Butterbur); ray-flowers $\varnothing$, disc-flowers $\varnothing$ $\varnothing$ $\varnothing$; sometimes diocious. Capitula in racemes or panicles. The leaves develop after flowering; they are deciduous; the receptacle is a noli- +tary capitulum borne on a scaly, scape-like stem; the ray- +flowers are $\varnothing$ with ligulate corollas, disc-flowers $\varnothing$. The leaves unfold after the flowering. Ageratum, Muhlenk., Vernonia. + +**F. Asteraceae**, Asteraceae Group. All the flowers are of two forms and different sexes; the ray-flowers are $\varnothing$ (sometimes neuter), most frequently with irregular, falsely +ligulate, radiating corollas; the disc-flowers are $\varnothing$, neuter, with + +572 +Dicotyledones. + +tubular corollas (Fig. 610). Sometimes only tubular flowers are present, as e.g. in *Scouio vulgaris* (Groundsel), and the exterior of the capitulum is then as in the Euphorbiaceae. The stamens branch out from the base of the corolla, and are inserted on its inner side. + +A. **ANTHEMIDEAE.** Involucral leaves imbricate, generally mem- +branous at the edge; pappus wanting, or at most a membranous margin to the calyx, but without hairs. + +1. *Chamaemelum* bracteolæ on the receptacle are found in *Anthemis* (Chamomile), *Aesculus* (Horse-chestnut), *Achillea* (Milfoil, Fig. 610). + *Saxifraga*, etc. + +**A.1.* A naked receptacle is found in the following: *Bellis* +(Cherry-Blossom) has capitula on leafless stalks with white ray- +flowers—*Matricaria* (White Chamomile) has a conical receptacle. +(*M. chamomilla* has a very high, hollow receptacle; *M. teucrium halarhaz*, odour- +ous capilla, and the receptacle is not hollow.)—*Chrysanthemum* (Ox- +eye) may have a naked receptacle; *Pseudosantonium* (False +Pyrethrum); *pappus* scanty.—With these are classed *Tussilago* +(Tansy) and *Artemisia* (Wormwood) with tubular corolla only. + +B. **HELIANTHEE.** Most frequently a bract to each flower is found on the receptacle, which is often a cup-like structure, but consists of scales, spines, etc., and the fruits are most frequently compressed (Fig. 606 c)—*Helianthus* (Sun-flower). *H. tuerberus* +(Jerusalem Artichoke) has tubercled underground stem. *Dahlia* +has tubercled underground stem also; *Cynara scolymus* (Artichoke), +the fruits are compressed with 2 (or more) spines provided with +reflexed barbs—*Callopsis*: *Bulbocodium*: *Zuava*: *Tugetea* has united involucral leaves, and yellow, transparent oil-glands. *Spalanches, +Gillenia*, *Umbelliferae*, *Sphagnus* (Compass-plant), *Helianthus, +Guillardia.* + +C. **CALESCEEAE** have 1–2 rows of involucral leaves, a naked +receptacle, and large, crescent-shaped, irregularly warded fruits, +of different kinds; as e.g. *Cacalia* (Cabbage), *Cauliflower*, pappus alate (Fig. +605 c)—*Calendula* (Marigold): ray-flowers white; pappus alate (Fig. +605 d). + +D. **SENCIOEEAE** have a fine, hairy, white pappus; no bracts; +otherwise as in Anthemideae. The involucral leaves are most +frequently imbricate—*Gypsophila*: *Grossularia*: *Lysimachia*, whorls +of involucral leaves, which most frequently have black tips, +the external being much shorter than the internal ones (*S. vulgaris +has all flowers & alike*)—*Cucullia*, *Doronicum*, *Glyceria, +Lobelia*, *Aronia* (*A. mansoni*: large, long-stalked capitula; leaves opposite, forming a kind of rosette.*) + +AGGREGATE. 573 + +E. ASTEREE have a bristle-like, unbranched pappus, often of a dingy brown; receptacle naked; involucral leaves numerous, im- +bricant.—Solidago (Goldenrod) - capitate small, yellow-flowered, bora; the corolla of the flowers more or less frequently yellow, +or flavoured violet; Callistephus; Erigeron (Fleshy-leafed). - Hand- +All the corollas are tubular in: Graphalium (Cult.-wood); involu- +cral leaves dry, rattling, often coloured; the foliage-leaves and +stems often white with woolly hairs; flower-stem 3-5, with narrow, +tubular corolla; the leaves alternate; Lysimachia (Chalk-foil; +dixionis), Filago, Helichrysum, Ammobium, Rhodanthe and others. +Lontopodium (L. dipinum, "Edelweiss"). + +F. AMBOREE, a very reduced type of Compositae, differing from the others in that the involucre is wanting, and the corolla is tubular. In this case, the +leaves are in a terminal inflorescence, the 3 in the leaf-axis. In other respects +they are most closely related to Helichrysum. - Leathria. In the 5-capitulum +there are 2 flowers only, which are sessile on a short peduncle; the in- +volucral leaves. In the 5-capitulum there are only 2 flowers, which are entirely +destinct of both calyx and corolla; involucral leaves 2-4-petaled, united to form +a cup-like structure, which encloses the flower-stem and its appendages. This envelope of involucral leaves unite with the fruite, enclosing them at maturity +with a hard covering from which numerous hooks like pin-joints project, assisting +the fruit in its descent from the plant. The fruit is a nutlet or a nut. The capsule finally +becomes a 1-celled 2-sepal fruit—nutlet. - Antheris - The capitulum is 1-celled. + +FILANTHUS. The filaments of these plants are long and become very com- +plicated by their being crowded together to one side of the flower. The corolla of the ray-flowers, being often very large (Latexia; Cessaea), fre- +quently becomes so long as to be almost thread-like. This is a very many +biological phenomenon similar to those shown by the individual flowers in +other orders, e.g. by periodically opening and closing, in which the involucral +leaves act as a kind of curtain over the flower-stem. The flower-stem separates +from the term "filum capillare", composite flower". An abundance of honey is formed, which so some extent fills up the nectar-bottle, and since insects may +be attracted by its sweetness to feed upon it, they are also attracted by very fre- +quently visited, especially by butterflies and bees. The pollination has been described on page 507. Prosemin is universal. In the bud the tips of the stamens are united into a tube which is prolonged into a long filament; but in the next stage the style grows through the tube and swells out to pass the pollen +at its process to reach the stigma. In many, the movements of the filaments assist +in sweeping out the pollen at the exact moment of the insect visit. Regular species of this genus are found in all parts of Europe; wild-poppywort e.g., in +Arenaria and the plants related to it. + +This extremely natural and well-defined order in the largest number (and no doubt +the most important) of flowering plants is represented by about one-tenth of all flowering plants. They are distributed over the whole globe, but are most numerous in temperate countries; the majority prefer open + +574 +DICOITILAXONEX. + +space; a smaller number are forest-forms. They abound especially in open districts in America. + +Among the plants whose frequent use may be mentioned: *Lemn* (especially in the Siberian part), *Bitter* plants, *Tannin*, volatile oils, fatty oils in the fruits. *Maximiliana:* "Herba" of *Artemisia albaeburnis* (Warmwood) and *maritima* (Maritime Wormwood); *Cynara cardunculus* (Cardoon), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silybum marianum), *Cynara scolymus* (Silyllum maria- nina); the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- matica; the unopened capsules of *Artemisia moritana*, var. stich- + +APPENDIX ON THE CLASSIFICATION OF PLANTS. + +By M. C. POTTER. + +The earliest systems of classification were derived from the properties and use of plants; and it was not until some two centuries ago that any scientific grouping of plants was attempted. +Aristotle and Theophrastus had adopted the groups of Trees, Shrubs and Herbs as the chief divisions of the Vegetable Kingdome; but Linnaeus, in his Systema Naturae, published by Linnæus and Ray as late as the end of the 17th century. The arrangement by which these three divisions were separated into smaller divisions was often founded upon a single character, such as the formation of the flowers, the colour of the leaves, or the shape of the corolla, etc. All these systems of classification which brought into close proximity plants distinguished by some one character alone, could only be considered as artificial, since plants related to one another in other respects belonged to different groups. +As the knowledge of the morphology, physiology, and function of plants increased, such systems were recognised as unscientific, and it became the aim of botanists to establish a natural system, founded upon mutual relationships, which would associate together each plant with all others having similar traits. + +The following are some of the chief systems of classification which will show the gradual development of the natural system, and may be of service to students making use of this text-book.¹ + +System of John Ray (1703). + +I. Monocotyledones. + A. Insectiferae (Flowering). + B. Perforatae (Flowering). + Dicotyledones. + Monocotyledones. + +II. Arbores. + A. Monocotyledones. + B. Dicotyledones. + +Ray was the first botanist who recognised the importance of the one or two seed-leaves of the embryo, and initiated the division of the flowering-plants into Monocotyledones and Dicotyledones. + +² For further references see Sachs, History of Botany; Lindley, Vegetable Kingdom; Le Mothe and Brethwaite, General System of Botany; etc. + +W.R. +P F + +570 APPENDIX ON THE CLASSIFICATION OF PLANTS. + +System of LINNAEUS (1783). +In his well known artificial system Linnaeus divided the Verte- +table Kingdom into four classes, based upon the number, +relative position and union of the stamens with regard to each +other, and also to the gynoeceum. +Glasm +I. Monogynous. Flowers with 1 stamen. +II. Diandrous. Flowers with 2 stamens. +III. Triandrous. Flowers with 3 stamens. +IV. Tetrandrous. Flowers with 4 stamens. +V. Pentandrous. Flowers with 5 stamens. +VI. Hexandrous. Flowers with 6 stamens. +VII. Heptandrous. Flowers with 7 stamens. +VIII. Octandrous. Flowers with 8 stamens. +IX. Enneandrous. Flowers with 9 stamens. +X. Decandrous. Flowers with 10 stamens. +XI. Undecandrous. Flowers with 11 to 19 stamens. +XII. Duodecandrous. Flowers with 20 or more stamens inserted on +the same anther. +XIII. Tridecandrous. Flowers with 20 or more stamens inserted on +the same anther. +XIV. Tetradecandrous. Flowers ditallye receptacle. +XV. Quindecandrous. Filaments united into a bundle +of 15 bundles. +XVI. Sexdecandrous. Filaments united into a bundle +of 16 bundles. +XVII. Septendecandrous. Filaments united together, +forming a bundle of 17 bundles. +XVIII. Octodecandrous. Filaments dichotomous, & q and q on the same plant. +XIX. Nonadecandrous. Filaments dichotomous, & q and q on different plants. +XX. Undecandrous. Filaments dichotomous, & q and q on different plants. +XXI. Duodecandrous. Filaments dichotomous, & q and q on different plants. +XXII. Tridecandrous. Filaments dichotomous, & q and q on different plants. +XXIII. Tetradecandrous. Filaments dichotomous, & q and q on different plants. +XXIV. Pentacontandrous. Flowering plants (Ferns, Mosses, Algae, Fungi). + +These classes were further divided into orders, according to the number of +stigmas, as follows: +Order I., Monocots, or Monocotyledons, e.g., Orchis (Orchid), Iris (Iris), +a Dock (Rumex), having 6 stamens and 6 styles, would be placed in Class VI., +Hexandrae, and Order II., Triginae, Class VII., Dicots, or Dicotyledons, with seeds +apparently naked, comprising the Legumes, Order III., Angiospermae, with +the seeds enclosed in a capsule (Burkea, Rhododendron), Class VIII., Equisetales, +Class IX., Spermatophytae, or Seed Plants, e.g., Siliqua (Silkworm), a Silkworm fruit a silicula +(Capsule); and Order II., Siliceae, fruit a silicula (Basiony). +Class X., Monocots, or Monocotyledons, e.g., all flowers perfect (Sonnet); Order II., Spermatophytae, flowers in the centre perfect, those at the circumference with pistils only (pistillate) imperfectual, e.g., Aster; Order III., Trifoliateae, flowers in the centre perfect those at the circumference imperfect (imperfectual), e.g., Coniums. + +Fragmentum of a natural system have also come down to us from Linnaeus, +who himself always recognized the imperfection of his artificial system. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
XIV.Diatryma.Stamens ditallye receptacle.
XV.Tetraedraea.Filaments united into a bundle of 4 bundles.
XVI.Pentadraea.Filaments united into a bundle of 5 bundles.
XVII.Sextendraea.Filaments united together forming a bundle of 6 bundles.
XVIII.Septendraea.Filaments dichotomous & q and q on the same plant.
XIX.Nonadraea.Filaments dichotomous & q and q on different plants.
XX.Undeadraea.Filaments dichotomous & q and q on different plants.
XXI.Deceadraea.Filaments dichotomous & q and q on different plants.
XXII.Tridecandraea.Filaments dichotomous & q and q on different plants.
XXIII.Tetradecandraea.Filaments dichotomous & q and q on different plants.
XXIV.Pentacontaeraea.Flowering plants (Ferns, Mosses, Algae, Fungi).
+ +APPENDIX ON THE CLASSIFICATION OF PLANTS. +577 + +System of ANTOINE LAURENT DE JESSIEU (1789). + +Acotyledones. Plants without cotyledons : Fungi, Ferns, Mosses, Algae, Naïades. + +Class I. + +Monocotyledones. Plants with one cotyledon : + +1. Stamens hypogynous. . . . . . . . . . . . . . . . II. +2. perigynous. . . . . . . . . . . . . . . . . III. +3. epigynous. . . . . . . . . . . . . . . IV. + +Dicotyledones. Plants with two cotyledons : + +1. APELLENIUM. Stamens epigynous. V. +2. Corolla hypogynous. VI. +3. Corolla hypogynous. VII. +4. Monogynum. Perigynous. VIII. +5. Anthera somatose. IX. +6. epigynous. X. +7. free. XI. + +2. POLYGYNUM. Stamens epigynous. XII. +8. hypogynous. XIII. +9. perigynous. XIV. + +4. Diclinus insculptus, male and female flowers on different plants; corolla generally absent. + +System of A.P.de CANDOLLE (1819). + +1. Vascularics. Plants with vascular bundles. + 1. EXOCYME. Vasculum bundle arranged in a ring. + A. Diplocarpaceae. Calyx and corolla present. + b. Thelypteridaceae. Calyx and corolla absent and hypogynous. + c. Galpiniferae. Corolla perigynous or epigynous; stamens inserted on the calyx. + d. Convolvulaceae. Corolla epigynous; stamens inserted on the corolla. + B. Monocarpaceae. Perianth simple. + +2. ENDOCYME. Vasculum bundle scattered, the youngest in the center. + A. Phanerogamae. Flowers present. + B Cryptogamae. Flowers absent. + +II. Cellulares. Vasculum bundle absent. + +1. POLYGAMIAE. Leaves present. +2. APETALAE. Leafless. + +A diagram showing the classification of plants according to Antoine Laurent de Jussieu's system. + +578 +APPENDIX ON THE CLASSIFICATION OF PLANTS. + +ROBERT BROWNE published in 1627 his discovery of the gymno- +spermry of the ovoides of the Coniferae and Cycadinae, and showed that the Gymnospermae, which had previously been chained with the Dicotyledons, must be regarded as an independent group. + +System of STEPHEN ENGLISH (1830-40) + +I. Thallophyta. No differentiation into stem and root. +1. Protocotylus. Class I. Algae; Class II. Lichenes. +2. Hymenophyta. Class III. Fungi. + +II. Cormophyta. Differentiated into stem and root. +1. Aconitaria. Stem growing at the point. + Anaplecta (Hyatites, Musci). + Protophyta (Ferns, etc.). + Dipterozites (Dipteris, etc.). + +2. Amphibia. Stem growing at the circumference (Monocotyle- + donia). + +B. Acanthophyta. Stem growing both at the point and circum- + ference. + Gnetophyta (Gnetum). + Azolla. Ferniiths single or absent. + Gnetales. Ferniiths gymnosperms. + Eudicotyledon. Vascular polypodians. + +System of A. BRONNIER (1843). + +I. Cryogamycetum. Plants without flower. + 1. Amphibia. Not differentiated into stem or leaf (Algae, Fungi, Lichenes). + 2. Acronemum. Plants with stem and leaf (Musciaceae, bilicines). + +II. Phanerogamum. Plants with flowers. + 3. Monocotyledoneae. + a. Alismaceae. Seeds with endosperm. + b. Eucalyptaceae. Seeds without endosperm. + +III. Dicotyledoneae. + a. Angiospermae. + b. Gamopetalae. + c. Dicotyledon. + +IV. Gymnospermae. + +APPENDIX ON THE CLASSIFICATION OF PLANTS. +579 + +System of John Linnæus (Vegetable Kingdom, 1645). + +* Asexual, or Flowerless Plants. + +I. Thallops. +II. Acrogens. +III. Rhizopods. + +Fructification springing from stem. + +Wood of stem young in the center; endoderm +single-celled, or with one or more permanent wood; +of stem always conical. + +IV. Endogens. +V. Dictyogena. + +Wood of stem at the circumference, always +concentric; endoderm, 2 or more. + +VI. Gymnogena. +VII. Eugens. + +System of Alexander Blau (1804). + +I. Bryophyta. +1. Tracheae (Alge, Fungi, Lichens). +2. Tracheobionta (Chamae, Monocotyledons). +II. Cormophyta. +1. Polyploida (Ferns, Equisetum). +2. Monocotyledons (Lycopsid). +3. Hymenophyta (Water ferns). +III. Anthophyta. +Grass-like. +1. Fruticose (Cyperaceae). +2. Accreted (Coniferae). + +Asexual. +1. Rhizomataledeae. +2. Juncogonoea. +3. Apodalea. +Sympatdala. +Eleutheropealae. + +W. HUMBOLDT published from 1840 to 1851 his researches upon the embryology of the Phanerogams, and upon the embryology and life-history of the Vascular Cryptogams, and established the phylogenetic connection existing between the Monocotyledons, Vascular Cryptogams and Phanerogams. + +580 +APPENDIX ON THE CLASSIFICATION OF PLANTS. + +System of Hooker and Baxter (Genera plantarum, 1862-1883). + +**DICOTYLEDONES.** + +I. POLYPETALAE. + +Series I. Thalamiiferae. Calyx most often free from the corolla. Petals unicarpellate or often 2-carpellate, Stamina or corolla deflexed, inserted on the receptacle, often with a short pedicel. Corolla usually regular. Carpels epigynous, or immersed in the receptacle. Endosperm usually abundant, fleshy, or absent. + +Order I. Ranunculaceae. +25. Dilleniaceae. +5. Calymperaceae. +5. Noliniaceae. +Cohort II. Ranunculeae. Stamina or corolla deflexed, or if definite then in B- 2-carpellate. Carpels epigynous, or immersed into loculi by spurious dissepiments, with parietal placentation. Endosperm absent or fleshy. + +Order II. Ranunculeae. +10. Papaveraceae. +11. Cruciferae. +16. Carduiaceae. +17. Brassicaceae. + +Cohort III. Polygonaleae. Stamina deflexite. Corolla usually perfectly or imperfectly bilocular. Micropyge very often compressed laterally. Filaments very often annulate and with a long style. + +Order III. Polygonaleae. +18. Tussilaginaceae. +29. Tamarindaceae. +Cohort IV. Caryophyllaceae. Stamina deflexite, or rarely erect. Corolla unilocular, or imperfectly bilocular. Placentation central, more rarely parietal. Micropyge infundibuliform, or rarely strongly compressed and trilocular. + +Order IV. Fraxinaceae. +22. Caryophyllaceae. + +Cohort V. Guttiferae. Sepals imbricate. Stamina usually 0-carpellate, placenta on the inner angles of the lomuli. Endosperm absent or fleshy. + +Order V. Elaeisaceae. +20. Hyacinthaceae. +27. Guttiferae. + +Order VI. Asteraceae. +29. Asteraceae. +Order VII. Asteraceae. +30. Asteraceae. +Order VIII. Asteraceae. +31. Asteraceae. + +Order IX. Asteraceae. +32. Asteraceae. +Order X. Asteraceae. +33. Asteraceae. + +Order XI. Asteraceae. +34. Asteraceae. +Order XII. Asteraceae. +35. Asteraceae. + +Order XIII. Asteraceae. +36. Asteraceae. +Order XIV. Asteraceae. +37. Asteraceae. + +Order XVII. Asteraceae. +40. Asteraceae. + +Order XVI. Asteraceae. +41. Asteraceae. + +Order XVIII. Asteraceae. +42. Asteraceae. + +Order XIX. Asteraceae. +43. Asteraceae. + +Order XXI. Asteraceae. +44. Asteraceae. + +Order XXII. Asteraceae. +45. Asteraceae. + +Order XXIII. Asteraceae. +46. Asteraceae. + +Order XXIV. Asteraceae. +47. Asteraceae. + +Order XXVII. Asteraceae. +50. Asteraceae. + +Order XXVI. Asteraceae. +51. Asteraceae. + +Order XXVIII. Asteraceae. +52. Asteraceae. + +Order XXIX. Asteraceae. +53. Asteraceae. + +Order XXXI. Asteraceae. +56. Asteraceae. + +Order XXXII. Asteraceae. +57. Asteraceae. + +Order XXXIII. Asteraceae. +58. Asteraceae. + +Order XXXIV. Asteraceae. +59. Asteraceae. + +Order XXXVII. Asteraceae. +60. Asteraceae. + +Order XXXVI. Asteraceae. +61. Asteraceae. + +Order XXXVIII. Asteraceae. +62. Asteraceae. + +Order XXXIX. Asteraceae. +63. Asteraceae. + +Order XLII. Asteraceaee + + + + + + + + + + + + + + + + + + + + + + + + +APPENDIX ON THE CLASSIFICATION OF PLANTS. +581 + +**Cohort VI. Mucilages.** Sepals valvate. Stamens usually 2 or mona- +diplostomous. Ovary separate, placenta on the inner angles of the loculi. Endo- +spern absent or finicky. +Order 36. **Tiliaceae.** +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* * * +* ** +**Series II. Disciflorae.** Calyx usually free from the corolla. Petals uniurate, +Stamens usually definite, inserted within, upon, or around the receptacle, +which is more often expanded as a disc. Ovary usually free, or embedded in +the disc. + +**Cohort VII. Gennales.** Disc usually as a ring between the stamens, or adnate to the staminal tube, or reduced to glands alternating with the petals, remaining as a disc or cup-like structure at the base of the corolla. + +Ovules most often 1–3 in each loculus, pendulous, raphes central. Leaves +ovular. +Order 54. **Lousea.** +\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ +\ \ \ \ 35. Humoritum. +\ \ \ \ 36. Pseudolusca. +\ 37. Zygophyllum. +\ 38. Geranium. +\ 39. Geranium. +Order 55. **Gentianae.** +\ 40. Simarubum. +\ 41. Odontoglossum. +\ 42. Dicentra. +\ 43. Melittis. +\ 44. Chelidonium. + +**Cohort VIII. Oleaceae.** Disc cupular or annular, free, or bearing the stamens +and petals on its edge. Gymnocarp entire. Ovules 1–3 in the unilocular ovaries, or 1–3 in each loculus, pendulous, raphes dorsal. Leaves simple. +Order 43. **Gentianae.** +\ Order 67. **Chelidoniaceae.** +\ Order 68. **Melittaceae.** + +**Cohort IX. Asteraceae.** Disc tubular or cupular on the edge, or covering its base. +Stamens inserted round the disc or affixed to its margin. Gymnocarp usually entire. Ovules most often two in each loculus, erect, raphes central, pendulous, or pendulous and pendulous. + +Order 47. **Chelidoniaceae.** +\ Order 69. **Euphorbiaceae.** +\ Order 70. **Amelopsideae.** +\ Order 71. **Asteraceae.** + +**Cohort X. Saxifragae.** Dicotyledons. +Stamens basally inserted on the corolla tube, or on the ovary. + +Ovules cten 1–3 in each loculus, ascending with central raphes, or reversed, or solitary and pendulous from an ascending funicle, or rarely so horizontally orientated. +Leaves palmate-pinnate compound simple or digitate. + +Order 51. **Begoniaceae.** +\ 22\. Sabiaceae. +Order 52\. **Coriariaceae.** +\ Order 55\. Morinaceae. + +**Series III. Calyciformiae.** Calyx-tube usually surrounding the corolla, or +adnate to it at its base, or sometimes free from it; ovules usually one per loculus, +or definite, inserted in the calyx-tube, or most often on the disc: lining the calyx- +tube. Ovary often enclosed by the calyx-tube, or inferior. + +581 + +582 APPENDIX ON THE CLASSIFICATION OF PLANTS. + +Cohort XI. Rosales. Carpels solitary, or free, or united at the base, more rarely at the apex; styles distinct, or very rarely united into a column, and usually separate. + +Order 66. Campanulaceae. +.. 57. Lagunariaceae. +.. 58. Salicaceae. +.. 59. Saxifragaceae. +.. 60. Cruciferae. + +Cohort XII. Myrtales. Ovary syncarpous, inferior, or enclosed in the calyces; usually divided into lobes; style distinct. Order 67. Oleaceae—5–7 in the locality. + +Order 68. Rhinoboraceae. +.. 66. Convolvulaceae. +.. 67. Lycoperidaceae. + +Cohort XIII. Papaverales. Ovary syncarpous, inferior or superior, enclosed in the calyx-tube or exclosed, unilocular with partial placentation, or divided into loculi; stigma distinct, one stigmata divided, or undivided. + +Order 69. Papaveraceae. +.. 72. Lousea. +.. 73. Turionaceae. +.. 74. Daisacaceae. + +Cohort XIV. Fumariales. Ovary syncarpous, inferior or superior, divided into loculi with sub-basal placenta, or more rarely unilocular with partial placentation. Styles distinct, or divided at the apex. Embryo curved or excentric. + +Order 75. Cactaceae. +.. Order 76. Ficoidae. + +Cohort XV. Umbelliferae. Ovary syncarpous, inferior, crowned by the dome, divided into loculi; or microcarpous; styles distinct or divided at the apex. Orules solitary and pendulous in the bud. + +Order 80. Umbelliferae. +.. 81. Arnicaeae. + +II. GAMOPETALAE. + +Series I. Inferm. Ovary inferior. Stamens equal to the lobes of the corolla, rarely fewer. +Cohort I. Buculareae. Stamina adnate to the corolla. Ovary 2-locular, bidentate; 1–2-carpelate. + +Order 83. Caprifoliaceae. +.. Order 84. Rubaceae. + +Cohort II. Asteraceae. Stamina adnate to the corolla. Ovary formed of 2 carpels, unilocular and 1-ovuled. + +Order 85. Valerianaceae. +.. 86. Dioscoreaceae. + +Order 87. Calyceraceae. +.. Order 88. Compositae. + +A page from a botanical classification book. + +APPENDIX ON THE CLASSIFICATION OF PLANTS + +583 + +**Colubri III.** *Campanulaceae.* Stamens generally free from the corolla. Corolla 2-6-leaved, sessile, most often 2-clefted. + +Order 9. *Stylidiaceae.* +* *90. Gooseneck* + +**Series II.** *Heteromecium.* Corolla most often superior. Stamens free from the corolla, opposite to, or double the lobes of the corolla, or, on its if epipetalous, or hypogynous, or perigynous, or perianthous. + +**Colubri IV.** *Eriocaulaceae.* Stamens double the lobes of the corolla, or alternating with them. Corolla 2-3-leaved. Stamens usually minute. + +Order 97. *Eriocaulaceae.* +* *97. Eriocaulon.* +* *98. Diapensia.* +* *99. Monotropus.* +* *97. Lemnoaceae.* + +**Colubri V.** *Fernandaceae.* Stamens equal to and opposite the lobes of the corolla, or alternate with a few central petals, or sterile. + +Order 98. *Fernandaceae.* +* *98. Fernandaea.* +* *97. Primulaceae.* + +**Colubri VI.** *Erebidae.* Stamens equal to and opposite the lobes of the corolla, or double, or 3x. Corolla few and large. Truss or sheath. + +Order 101. *Syracaceae.* +* *101. Syracum.* + +**Colubri VII.** *Bicarpellate.* Corolla most often superior. Stamens equal or fewer than the lobes of the corolla, and alternating with them. Carpus 2-, rarely 3-lobed. + +**Colubri VIII.** *Gentianales.* Corolla regular. Stamens equal to the lobes of the corolla, or 1-4, usually alternating with the carpus. Leaves generally opposite. + +Order 104. *Oleaceae.* +* *104. Olea.* +* *105. Oleaceae.* +* *106. Apocynaceae.* +* *105. Gentianaceae.* + +**Colubri VIII.** *Polypodiales.* Corolla regular. Stamens equal to the lobes of the corolla. Leaves generally alternate. + +Order 105. *Polypodiales.* +* *105. Polypodium.* +* *106. Bergenia.* + +**Colubri IX.** *Ferns.* Corolla most often irregular or bilabiate. Posterior stamens (if any) usually reduced to a staminode, or altogether absent. +Corolla 2-clefted, or 2-valved. + +Order 115. *Bergulariaceae.* +* *115. Bergularia.* +* *116. Orbeaceae.* +* *118. Colusmellaceae.* + +Order 116. *Gomortegaceae.* +* *116. Gomortega.* +* *120. Bignoniaceae.* +* *123. Bignonia.* +* *125. Acanthaceae.* + +Order 118. *Columbiceae.* +* *118. Columbium.* + +584 + +APPENDIX ON THE CLASSIFICATION OF PLANTS. + +Cohort X. Lamiaceae. Corollas most often irregular or oblique. Posterior stamens less than the others, most frequently reduced to a stamina or absent. Capsules, when present, usually 1-seeded, but sometimes with 2 seeds, the protostem calyx, indehiscent, and with one seed, or dehiscing into 2 or rarely 3, isocoloid scales. +Order 126. Hypericaceae. +I. 126a. Salviaeae. +Anomalous Order 127. Plantaginaceae. + +III. MONOCHLAMYDEAE. +Fremitiis simple, lobes or segments 1-3-lobate and often sepaloid, or small, or entire. +Series I. Cynareaeae. Enneameris frequuntly farnaciosa. Embryo curved, erectus, lateralis, or peripheralis, rarely straight. Ovules most frequently 1 in the ovary, or 1 in each loculus. Flowers q., in some genera unilocular or polygamous, in others rare. Stamens equal to the segments of the perianth, rarely fewer or more. +Order 128. Nystalaceae. +I. 128a. Blechnaceae. +II. 128b. Nystaleae. +III. 128c. Chloropaeae. + +Series II. Multiovulatae Aquaticae. Aquatica herba, submergendo. Ovary syncarpous; ovules numerous in each loculus or on each placenta. +Order 129. Hydrophytae. +I. 129a. Hydrophyceae. + +Series III. Multiovulatae Terrestres. Territorial truss or shrubra. Ovary syncarpous; ovules numerous in each loculus or on each placenta. +Order 130. Neptunaceae. +II. 130a. Gylaceae. + +Series IV. Monocarpiae. Ovary syncarpous, monospermous, or syncarpous; ovules generally solitary in each carpel, rarely 2 or few. Endosperm ovoida, fleshy, or rarely farnaciosa. Embryo very minute. +Order 131. Erythraceae. +I. 131a. Erythraea. +II. 131b. Mimoniaceae. + +Series V. Daphnaceae. Ovary monospermous, very rarely syncarpous, with 2-4 loculi; ovule in the ovary or in each loculus, solitary, or in pairs. Truss or shrubbra; leaves simple; flowers regular, opena, 1-3 sepalia. Stamens perigynous, equal to the lobes of the perianth, or double unless fewer. +Order 145. Lauriaceae. +I. 145a. Lauraceae. +II. 145b. Thymelaeaceae. + +Series VI. Achlamydeooreae. Ovary unilocular, 1-3 ovules. Ovules most frequently poorly developed before flowering. Seeds endospermous, + +Order 146. Fumariaceae. +I. 146a. Fumariae. +II. 146b. Elateriaceae. + +Order 147. Thymelaeaceae + +APPENDIX ON THE CLASSIFICATION OF PLANTS. +585 + +but without tests, either free in the pericarp or attached to its walls. Perianth generally perfect, sepals or petals. Filaments. + +Order 148. Santalaceae. +q 148. Santalum. + +Series VII. Urticeae. Flowers unisexual. Ovary epigynous or mono- +carpous, usually in one or two each locule, solitary, or in pairs. Endosperm copious, flaccid, or scanty, or absent. +Trees or shrubs, rarely herbs. Stipules few, or none, or minute, or absent. Styles equal in number to the carpels, not rarely bifid. + +Order 150. Euphorbiaceae. +q 150. Euphorbia. + +q 151. Balsamorhiza. +q 152. Myriocarpa. +q 153. Myriophyllum. +q 154. Hystrix. +q 155. Lomatium. + +Series VIII. Ordines Anomalous. +Anomalous Orders. + +Order 160. Gnetaceae. +q 160. Gnetum. + +GYMNOSPERMEÆ. + +Order 166. Cycadeae. + +MONOCOTYLEDONES. + +Series I. Microsporae. At least the inner series of the perianth petaloid. +Ovary inferior, united with the perianth, or free, sessile or b-locular, with axile placentation. +Seed many, numerous, without endosperm. + +Order 167. Hydrocharitaceae. +q 167. Durmanniae. + +Series II. Epigynae. At least the inner series of the perianth petaloid. +Ovary superior, epigynous. + +Order 168. Orchideae. +q 168. Orchideae. + +Order 170. Scutellariae. +q 170. Amaryllidaceae. +q 171. Bromeliaceae. +q 172. Dioscoreaceae. +q 173. Dioscorea. + +Series III. Coronateae. At least the inner series of perianth petaloid. +Ovary free, very rarely stipitate adnate at the base. Endosperm copious. + +Order 177. Euphorbiaceae. +q 177. Pontederiaceae. +q 180. Philodendraceae. + +Order 182. Xyridaceae. +q 182. Gomphrenaceae. +q 184. Bapatraceae. + +580 + +APPENDIX ON THE CLASSIFICATION OF PLANTS. + +Series IV. Calycinae. Perianth sepaloid, small, rigid, or herbaceous (inner series subptaloid or small). Ovary free. Endosperm copious. +Order 165. Filagriinae. +.. 165. Palmae. + +Series V. Nudiflorae. Perianth absent, or reduced to hairs or scales. Ovary superior, carpel solitary, or if many, synerchicous, 1-celled, endoapertum present. +Order 166. Filagriinae. +.. 166. Filagria. + +Order 183. Pandorinae. +.. 183. Cyanophytae. +.. 183. Cyanophyceae. +.. 183. Cyanophyta. + +Series VI. Apocarpae. Perianth 1-2-septate or absent. Carpels superior, solitary, or in pairs or clusters. Endosperm absent. +Order 184. Tristichinae. +.. 184. Alismataceae. + +Series VII. Glumaceae. Flowers solitary, sessile in the axils of bracts and arranged in a capitate or spike-like with bracts. Segments of perianth small, subhilar, or subapical, often persistent on the fruit; ovules few to many per locule. Endosperm present. +Order 185. Naiadinae. + +Series VIII. Thallophytae proposed by SACHS (Text-Book of Botany, English Edition, 1882). + +**THALLOPHYTES**. +Continuing chlorophyllid. +Class I. Phytophytes. +Cyanophytae. +Cyanophyceae (in part). +Palmariales (in part). +Class II. Zygosporae. +Conjugating cells motile. +Class III. Oospores. +Spirochaetae. +Vibrioideae. +Yolochion. +Oedogonium. +Puce-dam. + +Not containing chlorophyllid. +Class I. Phytophytes. +Cyanophytae. +Cyanophyceae (in part). +Palmariales (in part). +Class II. Zygosporae. +Conjugating cells motile. +Class III. Oospores. +Spirochaetae. +Vibrioideae. +Yolochion. +Oedogonium. +Puce-dam. + +Suproglogiums, +Peronosporens, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigasporae, +Gigaspora + +APPENDIX ON THE CLASSIFICATION OF PLANTS. +587 + +Class IV. Carposporomorpha. + +Coleschizomorpha. +Florideomorpha. +Characeomorpha. + +Ascomycetes (including Lichens). +Eodidymyces (Uredinae). +Bacidomyces. + +System of A. W. Euchlee (ISSS). + +A. Cryptogamia. + +I. Thallophyta. + +1. Class. Ascom. + 1 Group. Cyanophyceae. + 2 = Dicotomae. + 3 = Monocotylym. + 1 Series. Conjugatae. + 4 = Phycoporeae. + 5 = Characeae. + 4 Group. Phycoporeae. + 5 = Rhizoporeae. + +2. Class. Fungi. + 1 Group. Schizomyces. + 2 Emyrystes. + 3 = Bacidomyces. + 2 = Ustilaginum. + 5 = Eodidymyces. + 4 = Rhizoporeae. + 5 = Bacidomyces. + 6 Group. Lichenes. + +II. Bryophyta. + 1 Group. Hepaticae. + 2 Musci. + +III. Pteridophyta. + 4 Class. Equisetumia. + 4 = Lycosoria. + 5 = Filicinae. + +B. Phanerogamia. + +1. Gymnospermae. +2. Angiospermae. + +The subdivisions of the Phanerogamia have with little variation been adopted in this book. + +388 +APPENDIX ON THE CLASSIFICATION OF PLANTS. + +Classification of the THALLOPHYTES, adopted in the 3rd Danish Edition (1891). [Alge by Wille; Fungi by Rostrup (after Zopf.)] + +I. DIVISION. THALLOPHYTA. +1. Sub-division. Algae. + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +II. Sub-division. Mucoromycetes. + +III. Fungi. + +A. Phycomycetes. + +1 Class. Oecotricha. + +2 Class. Mycomycetes. + +A. Class. Basiomycetaceae. + +B. Sub-class. Ascomycetaceae. + +B. Family. +Hymenomycetes. +3 +Ascomycetes. +4 Class. Ascotricha. + +1 Family. +Gymnosporiaceae. +3 +Pyrenomycetes. +6 +Ascoblastes. + +
Class.Chlorophyceae (Green Algae).
1Fusarium.
2Pseudococcoides.
3Cordovales.
4Chlorophytes.
5Gymphytoes.
2 Class.Pirococcus (Brown Algae).
1 Family.Dinoflagellatae.
3Frytklypseae (Dinomites).
4Cyamopsicum.
5Dityroem.
3 Class.Acutiales.
A. Family.Schizaphytes.
B. Sub-class.Mycophyces (Blue-Green Algae).
1 Family.Bangioleae.
2Furidinae.
+ +APPENDIX ON THE CLASSIFICATION OF PLANTS. 589 + +System of A. Engler (Syllabus der Vorlesungen, etc., 1892). + +I. DIVISION. MYXOTHALLOPHYTA. +Sub-division. Myxomycetes. +1 Class. Archeiales. +2 ** Plasmodiophorales. +3 ** Ectocarpales. +1 Series. Ectocarpae. +2 ** Endocarpales. + +II. DIVISION. EUTHALLOPHYTA. +I. Sub-division. Schizophytae. +1 Class. Schizomycetes. +2 ** Schizontes. +II. Sub-division. Dimidiazellata. +1 Class. Dimidiazellae. +1 Series. Adulae. +2 ** Endodimidiazellae. +III. Sub-division. Bacillariatae. +Class. Bacillariales. + +IV. Sub-division. Gamophytaceae. +1 Class. Chlorophyceae. +1 Sub-class. Protococcidae. +2 ** Chlorococcidae. +3 ** Siphonidae. +8 Class. Chlorophytae. +4 ** Phycodryaceae. +1 Sub-class. Phycosporae. +2 ** Ductulatae. +5 Class. Ductulatae. +6 ** Rhodophyceae. +1 Sub-class. Rhodophyceae. +2 Florideae. +1 Series. Nemathelminthes. +2 ** Rhodinominae. +3 ** Rhodinominae. +4 Crypsomoninae. + +V. Sub-division. Fucophytae. +1 Class. Fucophyceae. +1 Series. Zygnemataceae. +2 ** Zygogynales. +1 Sub-series. Chytridiales. +2 Class. Monocotyledons. +1 Sub-class. Hemiaceli. +2 ** Hemibiodal. + +A diagram showing the classification of plants by A. Engler. + +309 + +APPENDIX OF THE CLASSIFICATION OF PLANTS. + +I. Class. MYCOBACTERIA. + 1 Sub-class. Ascocarci. + 1 Series. Eumyceti. + 2 Series. Chytridiomycetes. + 2 Sub-series. Gymnosporangiales. + 2 Sub-series. Peritrichiales. + 2 Sub-series. Pythiophyta. + Appendix. Fungi imperfecti. + 4 Sub-series. Hysteriales. + Appendix. Discomycetes. + 5 Sub-series. Basidiomycetes. + 1 Series. Basidiomycetales. + 1 Sub-series. Urediniales. + 1 Sub-series. Uredinales. + 2 Sub-series. Amaurosporales. + 3 Sub-series. Trichosporales. + 4 Sub-series. Filobasidiales. + 2 Series. Ascomycetales. + 1 Sub-series. Dacrymycetales. + 2 Sub-series. Hymenomycetales. + 3 Sub-series. Sphaeromycetales. + 4 Sub-series. Phialofores. + Appendix. Gasteromycetales. + Fungi imperfecti. + +III DIVISION. EMBRYOPHYTA ZOIDIOGAMA (Archaeog- +nialia). + I. Sub-division. Bryophyta (Musciinei). + 1 Class. Hartziales. + 1 Series. Anthocerotales. + 2 Jungenmamillales. + 3 Jungenmamillales. + 2 Series. + 2 Sub-series. Arrogariae. + +II. Sub-division. Pteridophyta. + + I. Class. Filicinae. + 1 Sub-class. Filicales. + 1 Series. Polypodiaceae. + 2 Sub-series. Tuberulathallus + 2 Sub-class. Hydropteridaceae. + +A page from a botanical classification book. + +APPENDIX ON THE CLASSIFICATION OF PLANTS. +501 + +2 Class. Equitalea. +1 Sub-class. Imperata. +2 Sub-class. Lycopodalea. +8 Class. Sphenophyllalea. +4 Sub-class. Lycopsidalea. +3 Sub-class. Lycopsidalea. +2 Sub-class. Heteroptera. + +IV. DIVISION. EMBRYOPHYTA Siphonogama. + +I. Sub-division. Gymnospermae. +1 Class. Coniferales. +2 Sub-class. Coniferales. +8 Sub-class. Pinaceales. +4 Sub-class. Gnetales. +II. Sub-division. Angiospermae. +1 Class. Magnoliidae. +Series. Verticillate. +2 Class. Magnoliidae. +1 Sub-class. Monocotyledonae. + +1 Series. Pandanales. +2 Series. Hedoniaceae. +3 Series. Gnetaceae. +4 Series. Pristimatae. +6 Series. Synanthae. + +X. Sub-class Dicotyledoneae. + +1 Group of Series. Archidendroideae. +1 Series. Fagales. +2 Series. Juglandales. +3 Series. Betulaceae. +4 Series. Fagales. +5 Series. Ulmaceae. +6 Series. Pteridales. +7 Series. Santalales. +8 Series. Aristolochiaceae. +9 Series. Papaveraceae. +10 Series. Centrospermae. +11 Series. Bannaniae. +12 Series. Rhinodendraceae. + +2 Group of Series. Sympetrae. + +1 Series. Ericales. +2 Series. Primulales. +3 Series. Myrtales. +4 Series. Coriariales. +5 Series. Tubuliform. + +W.R + +Q.Q + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
TABLE OF ABBREVIATIONS.
S = Sepals.P = Petals.F = Fronds.
A = Androecium.G = Gynaeceum.
$\varnothing$ = Male.$\varnothing$ = Female.
$\checkmark$ = Hermaproditie.
$\bigcirc$ = Indefl.;
+ +Names of continents and countries have sometimes been abbreviated, for example: Am.=America; As.=Asia; Af.=Africa; Ind.=India, etc. N., S., E., W.=North, South, East, West; Temp.=Temperate Regions; Trop.=Tropics. + +20F + +INDEX. + +Abelia, 556. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 131, 205, 130, 183. +Aber, 747. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilops. Aegilopsis. Aglaia-Flang., Gs., Hg., Alhagi., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., Bt., +Albion-Fungl.: Gs.; Hg.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; Alhagi.; +Albion-Fungl.: Gs.; Hg.; Alhagi.; +Albion-Fungl.: Gs.; Hg.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.; +Albion-Fungl.: Gs.*; +Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: Hg; +Algina-Flang: +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 +4 + +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babylonicae +Babyloniaea + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Berberis + +Bergeria. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beckmannia. + +Beekmaniiaceae + +504 + +INDEX + +Amannia, 483. +Ammi, 476. +Amaranthus, 494. +Amaranthus, 495. +Amaranthus, 496. +Amaranthus, 497. +Amaranthus, 498. +Amaranthus, 499. +Amaranthus, 500. +Amaranthus, 501. +Amaranthus, 502. +Amaranthus, 503. +Amaranthus, 504. +Amaranthus, 505. +Amaranthus, 506. +Amaranthus, 507. +Amaranthus, 508. +Amaranthus, 509. +Amaranthus, 510. +Amaranthus, 511. +Amaranthus, 512. +Amaranthus, 513. +Amaranthus, 514. +Amaranthus, 515. +Amaranthus, 516. +Amaranthus, 517. +Amaranthus, 518. +Amaranthus, 519. +Amaranthus, 520. +Amaranthus, 521. +Amaranthus, 522. +Amaranthus, 523. +Amaranthus, 524. +Amaranthus, 525. +Amaranthus, 526. +Amaranthus, 527. +Amaranthus, 528. +Amaranthus, 529. +Amaranthus, 530. +Amaranthus, 531. +Amaranthus, 532. +Amaranthus, 533. +Amaranthus, 534. +Amaranthus, 535. +Amaranthus, 536. +Amaranthus, 537. +Amaranthus, 538. +Amaranthus, 539. +Amaranthus, 540. +Amaranthus, 541. +Amarantaceae +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosa +Amargosaeae + +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. +6 +A page number "6" at the bottom left corner. + +INDEX + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagallis + +Anagalliaceae + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
INDEX.
Arrow-wood, 327, 431.Atheneum, 505.Dahuricum, 599, 298.
Arbutus, 886.Albireum, 204, 207, 213.Baeticaea, 321, 325.
Arctium, 573, 575.Atropa, 106.Beguia, 77, 78.
Arctium, 573.Atropa, 106.Beguia, 77, 78.
Arctium, 573.Atropa, 106.Beguia, 77, 78.
Arctium, 573.Atropa, 106.Beguia, 77, 78.
Arctium, 573.Atropa, 106.Beguia, 77, 78.
Arctium, 573.Atropa, 106.Beguia, 77, 78.
Jerusalem, 572, 574.Athelus, 227, 301.Berberis, 318.
Athelus, 227, 301.Athelus, 227, 301.Berberis, 318.
Athelus, 227, 301.Athelus, 227, 301.Berberis, 318.
Athelus, 227, 301.Athelus, 227, 301.Berberis, 318.
+ + +
ArbutusAthelusBerberis
AthelusAthelusBerberis
AthelusAthelusBerberis
AthelusAthelusBerberis
AthelusAthelusBerberis
AthelusAthelusBerberis
AthelusAthelusBerberis
AthelusAthelusBerberis
AthelusAthelusBerberis
AthelusAthelusBerberis
Atheum
+ + + + + + + + + + + + + + + + + + +
Index:Page Number(s):Page Number(s):Page Number(s):Page Number(s):Page Number(s):Page Number(s):Page Number(s):Page Number(s):Page Number(s):Page Number(s):Page Number(s):Page Number(s):Page Number(s):Page Number(s):Page Number(s):
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + +
Index:
+ + + + +
INDEX.

+ +
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
5061UXXK.
Pets, 309, 370, 372.Bonomiaalnecens, 83.Brunefalas, 291.
506.Hocca, 291.Bryacraum, 167.
Becksona, 538.Hocca, 292, 533.Bryophyllum, 451, 452.
Ictusy, 347.Hocca, 531.Bryophyllum, 453.
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Becksona, 541.Hocca, 534.Bryophyllum, 479,
Bryophyllum, +
201, +
202, +
203, +
206, +
208, +
209, +
210, +
211, +
212, +
213, +
216, +
218, +
219, +
220, +
221, +
222, +
223, +
226, +
228, +
229, +
230, +
231, +
236, +
238, +
239, +
240, +
241, +
246, +
248, +
250, +
251, +
256, +
260, +
261, +
268, +
270, +
271, +
276, +
280, +
281, +
286, +
288, +
289, +
290, +
291, +
296, +
300, +
301, +
306, +
308, +
309, +
310, +
316, +
318, +
319, +
320, +
326, +
330, +
336, +
338, +
339, +
340,
Bryophyllum +
Aquilegia +
Ferula +
Gentiana +
Lilium +
Muscari +
Narcissus +
Oenothera +
Paeonia +
Ranunculus +
Saxifraga +
Tulipa +
Vaccinium +
Xanthium +
Zinnia +
Zoysia +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus +
Zygopappus. +
Bryophyllum. +
Aquilegia. +
Ferula. +
Gentiana. +
Lilium. +
Muscari. +
Narcissus. +
Oenothera. +
Paeonia. +
Ranunculus. +
Saxifraga. +
Tulipa. +
Vaccinium. +
Xanthium. +
Zinnia. +
Zoysia. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
Zygopappus. +
ZYGOPAPPUS. + +INDEX. 597 + +1 + +2 + +3 + +4 + +5 + +6 + +7 + +8 + +9 + +10 + +11 + +12 + +13 + +14 + +15 + +16 + +17 + +18 + +19 + +20 + +21 + +22 + +23 + +24 + +25 + +26 + +27 + +28 + +29 + +30 + +31 + +32 + +33 + +34 + +35 + +36 + +37 + +38 + +39 +Calvular bean, 471. 478. +Calabash, 529. +Calabash, 530. +Calamagrostis, 299. 294. +Calamagrostis, 295. +Calamites, 294. +Calamites, 295. +Calamites, 303. +Calamus-olz, 896. +Calamus-olz, 897. +Calamus-olz, 898. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 899. +Calamus-olz, 89 +Cannabaceae. Cannabis sativa L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Cannabaceae. Cannabis indica L. +Canna +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canavalia +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canav利亚 +Canaviliae- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthago- +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Carthaginian, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, +Cataphracta, + +Aloe vera (L.) Burm.f., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barbadensis Mill., Aloe barb + +Aloes (Aloë vera) and (Aloë campestris).




























































+ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
5081DEX.
Centauri, 343.Chondraria, 299, 300, 301.
Centaurium, 847.Chondrus, 79, 83, 84.
"Centaur cell," 182.Chordia, 71.
Centaurium, 847.Chordia, 71.
Centropogon, 306.Chordia, 71.
Centropogon, 306.Chordia, 71.
Centrolobium, 476.Chordia, 71.
Centromerus, 476.Chordia, 71.
Centrum, 513.Chordia, 71.
Centrum, 513.Chordia, 71.
Cephalanthus, 482,Chordia, 71.
Cephalanthus, 482,Chordia, 71.
Cephalanthus, 482,Chordia, 71.
Cephalanthus, 482,Chordia, 71.
Cephalanthus, 482,Chordia, 71.
Cephalanthus, 482,Chordia, 71.
Cephalanthus, 482,Chordia, 71.
+ + +
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus
Cephalanthus79 + +Cirrus, 430 + +Cirrocumulus cil., 296. +Cirrocumulus, 401. +Cirrus, 437, 438. + +Cladocera, 500 +Cladodactylus, 108. +Cladonia, 193, 190, 141. +Cladonia, 193, 190, 141. +Cladophora, 111, 55. +Cladophora, 111, 55. +Cladophora, 111, 55. +Cladophora, 111, 55. +Cladophora, 111, 55. +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Clam, 342 +Cloverleafs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 800 +Cloverhairs. 801-816 +Cloverhairs. 817-866 +Cloverhairs. 867-966 +Cloverhairs. 967-996 +Cloverhairs. 997-1196 +Cloverhairs. 1197-1596 +Cloverhairs. 1597-1796 +Cloverhairs. 1797-1996 +Cloverhairs. 1997-2196 +Cloverhairs. 2197-2596 +Cloverhairs. 2597-2796 +Cloverhairs. 2797-3196 +Cloverhairs. 3197-3596 +Cloverhairs. 3597-5596 +Cloverhairs. 5597-7596 +Cloverhairs. 7597-9596 +Cloverhairs. 9597-11596 +Cloverhairs. 11597-15596 +Cloverhairs. 15597-17596 +Cloverhairs. 17597-19596 +Cloverhairs. 19597-21596 +Cloverhairs. 21597-25596 +Cloverhairs. 25597-27596 +Cloverhairs. 27597-31596 +Cloverhairs. 31597-35596 +Cloverhairs. 35597-55596 +Cloverhairs. 55597-75596 +Cloverhairs. 75597-95596 +Cloverhairs. 95597-115596 +Cloverhairs. 115597-155596 +Cloverhairs. 155597-175596 +Cloverhairs. 175597-195596 +Cloverhairs. 195597-215596 +Cloverhairs. 215597-255596 +Cloverhairs. 255597-275596 +Cloverhairs. 275597-315596 +Cloverhairs. 315597-355596 +Cloverhairs. 355597-555596 +Cloverhairs. ...Clovers with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clover plant with green leaves and yellow flowers.Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background. + +Clove flower petals on a clove leaf background.11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 +Coriander. 11 + +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. oleracea +Crassula oleracea var. olerace... +Due to copyright restrictions this page cannot be reproduced without permission. + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.cardunculus + +Cynara cardunculus subsp.carduncus... + +Due to copyright restrictions this page cannot be reproduced without permission. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Daucus carota L. + +Due to copyright restrictions this page cannot be reproduced without permission. + +Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbia lathyris H.B.K., Euphorbi... +Due to copyright restrictions this page cannot be reproduced without permission. + +Foeniculum vulgare Mill. + +Foeniculum vulgare Mill. + +Foeniculum vulgare Mill. + +Foeniculum vulgare Mill. + +Foeniculum vulgare Mill... + +Due to copyright restrictions this page cannot be reproduced without permission. + +Galeopsis speciosa (L.) Rchb.f. + +Galeopsis speciosa (L.) Rchb.f... + +Due to copyright restrictions this page cannot be reproduced without permission. + +Glycine max (L.) Merril + +Glycine max (L.) Merril... + +Due to copyright restrictions this page cannot be reproduced without permission. + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Hedera helix (L.) A.Juss... + +Due to copyright restrictions this page cannot be reproduced without permission. + +Helianthus annuus L. + +Helianthus annuus L. + +Helianthus annuus L. + +Helianthus annuus L.... + +Due to copyright restrictions this page cannot be reproduced without permission. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Helichrysum italicum Mill.. + +Due to copyright restrictions this page cannot be reproduced without permission. + +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosella Scop... +Hieracium pilosell... + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
INDEX.001
Dahila, 509; 572.Ichneumon, 516.Dysporeusnanae, 415.
Dalysa, 572.Dichroa, 516.Dysporus, 415.
Dalysia, 472.Dichroa, 516.Dysporus, 415.
Dalysia, 472.Dichroa, 516.Dysporus, 415.
Dalysia, 472.Dichroa, 516.Dysporus, 415.
Dalysia, 472.Dichroa, 516.Dysporus, 415.
Dalmatia, 883.Dichroa, 516.Dysporus, 415.
Dalmatia, 883.Dichroa, 516.Dysporus, 415.
Dalmatia, 883.Dichroa, 516.Dysporus, 415.
Dalmatia, 883.Dichroa, 516.Dysporus, 415.
Dalmatia, 883.Dichroa, 516.Dysporus, 415.
Dalmatia, 883.Dichroa, 516.Dysporus, 415.
+ + + +
IndexPageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +PageDescriptionPage Number +
+ + + +
Asthenes
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
Dahila
Dalysia
Dalmatia
+ + + +
Asthenes
Dahila
Dalysia
Dalmatia
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes
+ + + +
Asthenes.










































































<429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 +429 + +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippocastanum +Aesculus hippo... +AESCULUS HIPPOCASTANUM + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farnesiana + +Acacia farn... +AESCULUS HIPPOCASTANUM + +Actaea racemosa + +INDEX. 603 + +Exuviaii, 16, 17, 21. +Ipe-keghla, 325. +Jatropha, 289. +Faba, 406, 470, 471. +Palma, 591. +Pistacia, 397. +" Fichel," 294. +Ferula, 295. +Ferulae-aurantiaceae, 84. +Fagoma, 405. +Fagopyrum, 541, 549. +" Fairy-vines," 88, 186. +" Falcaria," 494. +" Falcaria," 494. +Fascia-palm, 195. +Fasciole, 203. +Faiton, 621. +Faginaceae, 294. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 299. +Faguar-palm, 29 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603 +603Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia,Ficus-angustifolia, +Index Item: Ficus angustifolia +Description: Ficus angustifolia +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 603 +Page Number: 6 + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
G04IIXLX
Genipa, 550.Guava, 600.
Genipa, 573.Guava, 613.
Geniparum, 471.Guava, 625.
Geniparum, 541.Guava, 635.
Geniparum, 548.Guava, 645.
Geniparum, 843.Guava, 655.
Geniparum, 849.Guava, 665.
Geniparum, 851.Guava, 675.
Geniparum, 853.Guava, 685.
Geniparum, 859.Guava, 695.
Geniparum, 861.Guava, 705.
Geniparum, 863.Guava, 715.
Geniparum, 869.Guava, 725.
Geniparum, 871.Guava, 735.
Geniparum, 873.Guava, 745.
Geniparum, 879.Guava, 755.
Geniparum, 881.Guava, 765.
+ + +
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia
Gnomaia605 + +Halymenia, 84. +Halmiella, 37, 45. +Hamamelis, 45. +Hammondia, 45. +Hankukul, 54. +Hapalopilum, 57. +Haplophryne, 192. +Haplomora, 73. +Haplospira, 13. +Hazel-fern, 314. +Hazell, 192. +Hart's-tongue, 314. +Hart's-wort, 314. +Hasenbachia, 352. +Hasenbushia, 352. +Hasenfussia, 352. +Hasenfrutella, 352. +Haskinsia, 317. +Hawkbeard, 571. +Hawkthorn, 660. +Hay-basilum, 97, 89, 99. +Hay-scented fern, 314. +Hazel-nut, 848. +Hazelnut, 848. +Heath, 507. +Heath-fern, 241. +Hechtia, 319. +Hechtia-montana, 319. +Heide-moss, 319. +Heidemannia, 319. +Heide-moss-fern, 319. +Heide-moss-fern-plant, 319. +Heide-moss-fern-plant-plantlet, 319. +Heide-moss-fern-plant-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet-plantlet +Heide-moss-plant +Heide-moss-plant-plant +Heide-moss-plant-plant-plant +Heide-moss-plant-plant-plant-plant +Heide-moss-plant-plant-plant-plant-plant +Heide-moss-plant-plant-plant-plant-plant-plant +Heide-moss-plant-plant-plant-plant-plant-plant-plant +Heide-moss-plant-plant-plant-plant-plant-plant-plant-plant +Heide-moss-plant-plant-plant-plant-plant-plant-plant-plant-plant +Heide-moss-plant-plant-plant-plant-plant-plant-plant-plant-plant-plant +Heide-moss-plant-plant-plant-plant-plant-plant-plant-plant-plant-plant-plant +Heide-moss-plant-plant-plant-plant-plant-plant-plant-plant-plant-plant-plant +Heide-moss-plants +Heide-mosses +Heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-heide-mosses-hede +Heidemannia-helvetica +Heidemannia-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica-helvetica +Helianthus +Helianthus-andersonii +Helianthus-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii-andersonii +Helianthus-bellus +Helianthus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus-bellus +Helianthus-carnifex +Helianthus-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex-carnifex +Helianthus-densiformis +Helianthus-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis-densiformis +Helianthus-facundoi +Helianthus-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facundoi-facun +Helianthus-gigantea +Helianthus-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigantea-gigangee-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a-a +Helianthus-granulosum +Helianthus-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granulosum-granuloso-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s-s- +Helianthus-johnsoniae +Helianthus-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoniae-johnsoe-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e-e- +Helianthus-kansasensis +Helianthus-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasensis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis-kansasesis +Helianthus-lanceolatus +Helianthus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatus-lanceolatu... +Helianthus-leucanthemoides +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianthus-leucanthemoid... +Helianhus-tuberosus +Heliocarpella-pachyderma +Heliocarpella-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderma-pachyderm... + +606 + +INDEX. + +Hydroclea, 515. +Hydrophyllum, 515. +Yogurtseed, 205, 215. +308. +Hydronephros, 16. +Hydronephrosis, 17. +Hygroscopic, 172. +Hygroscopicum, 197. +Hygroscopicum, 200. +Yogurtseed, 205. +Yogurtseed, 206. +Yogurtseed, 207. +Yogurtseed, 208. +Yogurtseed, 209. +Yogurtseed, 210. +Yogurtseed, 211. +Yogurtseed, 212. +Yogurtseed, 213. +Yogurtseed, 214. +Yogurtseed, 215. +Yogurtseed, 216. +Yogurtseed, 217. +Yogurtseed, 218. +Yogurtseed, 219. +Yogurtseed, 220. +Yogurtseed, 221. +Yogurtseed, 222. +Yogurtseed, 223. +Yogurtseed, 224. +Yogurtseed, 225. +Yogurtseed, 226. +Yogurtseed, 227. +Yogurtseed, 228. +Yogurtseed, 229. +Yogurtseed, 230. +Yogurtseed, 231. +Yogurtseed, 232. +Yogurtseed, 233. +Yogurtseed, 234. +Yogurtseed, 235. +Yogurtseed, 236. +Yogurtseed, 237. +Yogurtseed, 238. +Yogurtseed, 239. +Yogurtseed, 240. +Yogurtseed, 241. +Yogurtseed, 242. +Yogurtseed, 243. +Yogurtseed, 244. +Yogurtseed, 245. +Yogurtseed, 246. +Yogurtseed, 247. +Yogurtseed, 248. +Yogurtseed, 249. +Yogurtseed, 250. +Yogurtseed, 251. +Yogurtseed, 252. +Yogurtseed, 253. +Yogurtseed, 254. +Yogurtseed, 255. +Yogurtseed, 256. +Yogurtseed, 257. +Yogurtseed, 258. +Yogurtseed, 259. +Yogurtseed, 260. +Yogurtseed, 261. +Yogurtseed, 263. +Ilex. 444. +Ilex. 445. +Ilex. 450. +Ilex. 451. +Ilex. 458. +Ilex. 467. +Ilex. 471. +Ilex. 478. +Ilex. 489. +Ilex. 498. +Ilex. 508. +Ilex. 517. +Ilex. 537. +Ilex. 547. +Ilex. 567. +Ilex. 570. +Ilex. 573. +Ilex. 578. +Ilex. 589. +Ilex. 609. +Ilex. 619. +Ilex. 639. +Ilex. 669. +Ilex. 689. +Ilex. 709. +Ilex. 719. +Ilex. 739. +Ilex. 769. +Ilex. 789. +Ilex. 809. + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritimus. Juncus maritimus + +Juncus maritinus. Juncus maritinus + +Juncus arcticus. Juncus arcticus + +Juncus arcticus. Juncus arcticus + +Juncus arcticus. Juncus arcticus + +Juncus arcticus. Juncus arcticus + +Juncus arcticus. Juncus arcticus + +Juncus arcticus. Juncus arcticus + +Juncus arcticus. Juncus arcticus + +Juncus arcticus. Juncus arcticus + +Juncus arcticus. Juncus arcticus + +Juncus arcticicus (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds., synon.: Junci arctici (L.) Huds.,syno + +INDEX. 607 + +Labyrinthus Fungus, 166. +Laxifolius, 135. +Lecanium, 142. +Lecanora, 142. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lectoria, 368. +Lecanum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. +Leucobryum, 142. + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 + +507 +R R + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
608INDEX.
Louiseira, 533, 554, 556.Macropodium.941.Marmara, 327.
Louiseira, 534, 556.Macropus, 300, 312, 343.Macropus, 300, 312, 343.Marmara, 171.
Louiseira, 534, 556.Marmoseta, 72.Marmoseta, 72.Marmara, 171.
Louiseira, 534, 556.Mastaxia, 198.Mastaxia, 198.Marmara, 171.
Louiseira, 534, 556.Maubertia, 552, 553.Maubertia, 552, 553.Marmara, 171.
Louiseira, 534, 556.Medicago, 192.Medicago, 192.Marmara, 171.
Louiseira, 534, 556.Meles, 818.Meles, 818.Marmara, 171.
Louiseira, 534, 556.Melesa,Melesa,Marmara, 171.
Louiseira, 534, 556.Massa,Massa,Marmara, 171.
Louiseira, 534, 556.Massa,Massa,Marmara, 171.
Louiseira, 534, 556.Massa,Massa,Marmara, 171.
Louiseira, 534, 556.Massa,Massa,Marmara, 171.
Louiseira, 534, 556.Massa,Massa,Marmara, 171.
Louiseira, 534, 556.Massa,Massa,Marmara, 171.
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
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Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:
Louvainia:609 + +Melanoseumium, 497. +Melanoseumia, 492. +Melanoseumia, 493. +Melanoseumia, 498. +Melanoseumia, 500. +Melastomaceae, 485. +Melastomaceae, 486. +Melastomaceae, 487. +Melastomaceae, 488. +Melastomaceae, 489. +Melastomaceae, 490. +Melastomaceae, 491. +Melastomaceae, 492. +Melastomaceae, 493. +Melastomaceae, 494. +Melastomaceae, 495. +Melastomaceae, 496. +Melastomaceae, 497. +Melastomaceae, 498. +Melastomaceae, 499. +Melastomaceae, 500. +Microaena, 15. +Micropyx, 245. +Micropyx, 246. +Micropinna, 131. +Micropinna, 132. +Micropinna, 133. +Micropinna, 134. +Micropinna, 135. +Micropinna, 136. +Micropinna, 137. +Micropinna, 138. +Micropinna, 139. +Micropinna, 140. +Micropinna, 141. +Micropinna, 142. +Micropinna, 143. +Micropinna, 144. +Micropinna, 145. +Micropinna, 146. +Micropinna, 147. +Micropinna, 148. +Micropinna, 149. +Micropinna, 150. +Micropinna, 151. +Micropinna, 152. +Micropinna, 153. +Micropinna, 154. +Micropinna, 155. +Micropinna, 156. +Micropinna, 157. +Micropinna, 158. +Micropinna, 159. +Micropinna, 160. +Micropinna, 161. +Micropinna, 162. +Micropinna, 163. +Micropinna, 164. +Micropinna, 165. +Micropinna, 166. +Micropinna, 167. +Micropinna, 168. +Micropinna, 169. +Micropinna, 170. +Micropinna, 171. +Micropinna, 172. +Micropinna, 173. +Micropinna, 174. +Micropinna, 175. +Micropinna, 176. +Micropinna, 177. +Micropinna, 178. + +Morellus. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 +Morcelliunum. 20 + +Morsellus. 20 +Morsellus. 20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 +Morsellus. 20-20 + +Moschella. 38-38
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
Moschella.
M
Mos
Mos
Mos
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Mos
Mos
Mos
Mos
Mos
Mos
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Mos
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Mos
Mos
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Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
Mos
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Mos
Mos
Mos
Mos
Mos
Mos
Mos
A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.A small image of a plant with green leaves and a brown stem.Description: A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside of the leaf showing the veins running parallel to each other in an intricate pattern. + +A close-up view of the underside + +610 + +Myristicaeae, 303. +Myrsinaceae, 200, 553. +Myrcium, 478. +Myrrh, 494. +Lavandula, 117. +Myrtus, 495, 496. +Myrtaceae, 200. +Myrtenum, 518. +Myrtaceae, 200. +Myrtus, 495. +Myrtaceae, 200. +Myrtle, 495. +Myrtaceae, 200. +Myrtle, 487, 488. +Myrtaceae, 200. +Myxomycetes, 66. +Myxomycota, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 66. +Mycetites, 67 +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narcissus +Narzisse + +INDEX. + +
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+ +IIXVII. + +611 + +Ophiola, 151. +Orchis, 370, 381, 332, 333 +Orobanche, 105 +Osmunda, 601 +Ornithogalum, 4 +Origanum, 536, 291, 541 +Ornithogalum, 409 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, 472 +Ornithoglossum, 469, +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303 +Palm-wine. 303
+Pamphlet-leafed-plantain. 185 +Panaxia-dimidiata. 185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. 185-185 +Panaxia-dimidiata. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVII. +Page number: IXXVIII + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
612INDEX
Pentaphylax95, 116.
Fallosa, 535.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
Persicula, 305.
+ + + +
FilaFila, S53.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora, S78.
Flora,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
FilaFila,
+ + + +
Pentaphylax
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
Fallosa
F
+ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
INDEX
Pentaphylax +Fallosa +Fallosa +Fallosa +Fallosa +Fallosa +Fallosa +Fallosa +Fallosa +Fallosa +Fallosa +Fallosa +Fallosa +Fallosa +Fallosa +Fallo + +INDEX + +613 + +Fahnia, 414. +Platyrhium, 313. +Platycentrus, 562. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. +Platymetra, 285. + +614 + +INDEX. + +Puya, 315. +Pyrophyllum, 50. +Pyrophyllum, 50. +Pyrophyllum, 50. +Pyrophyllum, 148. +Pyrophyllum, 35, 116. +Pyrophyllum, 148. +Pyrophyllum, 172, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyrophyllum, 374. +Pyphylliums. See Pyphylliums. + +Bay-flowers. See Bay-flowers. + +Baccharis. See Baccharis. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariola. See Beccariola. + +Beccariolae. See Beccarioles. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraria. See Becerraria. + +Becerraiaiisiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiusiiu + +INDEX. 615 + +Bulia, 351, 592, 553. +Rubusnica, 242, 545, 402. +Rubusnica, 400, 505, 548. +Rutaceae, 171. +Iubanis, 410, 460, 461. +Jubaea, 399, 400. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 330. +Bacillus, 417. Sandal-wood. 47, 50. +Sandaraceae. 269, 269. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492. +Sarcolepidium. 492, 492 +Sarcolepidium. 492 +Sarcolepidium. 492-511 +Sarcolepidium. 511-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518-518 +Sarcolepidium. 518- + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
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INDEX - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Selaginellaceae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleguinae - Seleyaiaea. + +INDEX. +617 + +Sjæveloben, 371, 400. +Sjærlodme, 44. +Sjærløb, 58. +Sjærløb, 177. +Sjærløb, 239. +Sjærløb, 439. +Sjærløb, 440. +Sjærløb, 487. +Sjærløb, 587. +Sjærløb, 687. +Sjærløb, 88. +Sjærløb, 100. +Sjærløb, 107. +Sjærløb, 108. +Sjærløb, 109. +Sjærløb, 112. +Sjærløb, 239. +Sjærløb, 250. +Sjærløb, 251. +Sjærløb, 252. +Sjærløb, 253. +Sjærløb, 254. +Sjærløb, 255. +Sjærløb, 256. +Sjærløb, 257. +Sjærløb, 258. +Sjærløb, 259. +Sjærløb, 260. +Sjærløb, 261. +Sjærløb, 262. +Sjærløb, 263. +Sjærløb, 264. +Sjærløb, 265. +Sjærløb, 266. +Sjærløb, 267. +Sjærløb, 268. +Sjærløb, 269. +Sjærløb, 270. +Sjærløb, 271. +Sjærløb, 272. +Sjærløb, 273. +Stereoconus, 148. Stereocerus, 150. Stereocerus, 149. Stereocolumella, 144. Stereocolumella, 145. Stereocolumella, 146. Stereocolumella, 147. Stereocolumella, 148. Stereocolumella, 149. Stereocolumella, 150. Stereocolumella, 151. Stereocolumella, 152. Stereocolumella, 153. Stereocolumella, 154. Stereocolumella, 155. Stereocolumella, 156. Stereocolumella, 157. Stereocolumella, 158. Stereocolumella, 159. Stereocolumella, 160. Stereocolumella, 161. Stereocolumella, 162. Stereocolumella, 163. Stereocolumella, 164. Stereocolumella, 165. Stereocolumella, 166. Stereocolumella, 167. Stereocolumella, 168. Stereocolumella, 169. Stereocolumella, 170. Stereocolumella, 171. Stereocolumella, 172. Stereocolumella, 173. Stereocolumella, 174. Stereocolumella, 175. Stereocolumella, 176. Stereocolumella, 177. Stereocolumella, 178. Stereocolumella, 179. Stereocolumella, 180. Stereocolumella, 181. Stereocolumella, 182. Stereocolumella, 183. Stereocolumella, 184. Stereocolumella, 185. Stereocolumella, 186. Stereocolumella, 187. Stereocolumella, 188. Stereocolumella, 189. Stereocolumella, 190. Stereocolumella, 191. Stereocolumella, 192. Stereocolumella, 193. Stereocolumella, 194. Stereocolumella, 195. Stereocolumella, 196. Stereocolumella, 197. Stereocolumella, 198. Stereocolumella, 199. + +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 +Stereoconus (cont'd), p. 60 + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +Sticodermum + +618 + +INDEX. + +Tabellariae, 21. +Tetramoriums, 544. +Tetragonisca, 307. +Tetraonidae, 572. +Tetramelus, 435. +Tetrapodidae, 295. +Tetrapus, 434. +Tetramorium, 411. +Tetramoriums, 411. +Tetramoriums, 407. +Tetramoriums, 407. +Tetramoriums, 412. +Tetramoriums, 412. +Tetramoriums, 572. +Tetramoriums, 572. +Tetramoriums, 573. +Tetramoriums, 573. +Tetramoriums, 591. +Tetrapus, 435. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. +Tetracerae, 206. + +INDEX. 619 + +Trizonia, 321. +Trionemota, 694. 425. +Tridactylus, 807. 314. +Triglottis, 100. 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Trigonella, 419. +Ureaa. 285. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. Ureum. 625. + +Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Venturia: Tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae tentoniae ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria ventoria venthoriai. + +Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ureaa; Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva Ulva UlvaUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvsUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvUlvU lvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulvulv uluvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuuvuu uuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuuu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu uu u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u u i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i i ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii ii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iii iiiiii iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv iv vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvi vvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvvivvviiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiiriiririririririririririririririririririririririririririririririririririririririririririririrrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirrirri rrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrii iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri iri 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s m s m s m s m s m s m s m s m s m s m s m s m s m s m s mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mm mmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmmm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:mm:m o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo oo ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee ee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee eeee ett ett ett ett ett ett ett ett ett ett ett ett ett ett ett ett ett ett ett ett ett ett ett ettt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt ttt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt tt ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk ttk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tk tktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktktkkktkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkkk k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k k kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kk kgg ggg ggg ggg ggg ggg ggg ggg ggg ggg ggg ggg ggg ggg ggg ggg ggg ggg ggg ggg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg gggg hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhh hhhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhh hhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH HH H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H H HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HH HIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIHIIIIIIIIIIIIIIIIIIIIIIIIIIIII III III III III III III III III III III III III III III III III III III III III III III III III III III III III III III III II II II II II II II II II II II II II II II II II II II II II II II II II II II II II II I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I I llllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllllll l ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll ll l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l bbbbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bbbb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bb bbbbb bbbb bbbb bbbb bbbb bbbb bbbb 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BC BC BC BC BC BC BC BC BC CC C C C C C C C C C C C C C C C C C C C C C C C C C C C C C C C C C C C CC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCC CCCCCC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CC CCCCC DDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDD D D D D D D D D D D D D D D D D D D D D D D D D D D D D D D D D D D D DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DD DDS S S S S S S S S S S S S S S S S S S S S S S S S S S S S S S S S S S SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SS SSSSS TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT T T T T T T T T T T T T T T T T T T T T T T T T T T T T T T TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT TTTT PQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQ QQ Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q Q QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQ QQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQQ OOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOO O O O O O O O O O O O O O O O O O O O O O O O O O O OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO OO 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cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc cccc ccccCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECECE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CE CeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCeCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCcCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCHCH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH CH + +0/20 + +INDEX. + +Water-salt, 22. +Water-purslane, 483. +Water-plantain, 296. +Water-wort, 415. +Waggoner, 371. +Wax-flower, 346. +Weberia, 354. +Weigilia, 354. +Weinbergia, 294. +Weinhaeusera, 267. +Welwitschia, 267. +Wendlingera, 67. +West Indian arroz-grain, 817. +White bean, 217. +Wheat, 131, 291, 292, 295. +Wheat-grain, 292. +Wheat seedling, cf. 292. +White cabbage, 461. +White clover, 461. +White mustard, 405. +White onion, 405. +White pepper, 365. +White radish, 365. +White Rape-fly, 387. +Whiteweed, 387. +Whitewort, 387. +Willow Balsam, 540. +Willow Cabbage, 540. +Wildeye, 194, 193, 309. +Winter aconite, 831. +Winter cherry, 831. + +Winter-cress, 451. +Winter green, 507. +Wintergreen-leaved mint, 507. +Wintergreen-leaved mint-leaves, 507. +Wintergreen-leaved mint-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-leaves-... +Wintergreen-mint, cf. Wintergreen-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint-mint... +Wintergreen-plantain, cf. Wintergreen-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain-plantain... +Wintergreen-tarweed, cf. Wintergreen-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed-tarweed... +Wintergreen-willowherb, cf. Wintergreen-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb-willowherb... +Wintergreen-yellowflower, cf. Wintergreen-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower-yellowflower... +Wintergreen-white-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered-sky-blue-flowered... +Wintergreen-white-spotted-buttercup, cf. Wintergreen-white-spotted-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup-buttercup... +Wintergreen-white-spotted-daisy, cf. Wintergreen-white-spotted-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy-daisy... +Wintergreen-white-spotted-goldenrod, cf. Wintergreen-white-spotted-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod-goldenrod... +Wintergreen-white-spotted-hawkbit, cf. Wintergreen-white-spotted-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit-hawkbit... +Wintergreen-white-spotted-lupine, cf. Wintergreen-white-spotted-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine-lupine... +Wintergreen-white-spotted-plumegrass, cf. Wintergreen-white-spotted-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass-plumegrass... +Wintergreen-white-spotted-rabbitbrush, cf. Wintergreen-white-spotted-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbrush-rabbitbr... +Wintergreen-white-spotted-robin-of-the-valley, cf. Wintergreen-white-spotted-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-the-valley-robin-of-th... +Wintergreen-white-spotted-stemmed-fringeleaf,... + +A blank page with a faint, circular pattern in the center. + +3 + +108 + +A black background with a faint, vertical line on the right side. + +UNIVERSITY OF TORONTO +LIBRARY + +Do not +remove +the card +from this +Pocket. + +Acme Library Card Pocket +Under Pen. "See Library Policy" +Made by LIBRARY BUREAU, Boston + +A black and white image of a person's face, possibly a woman, with dark hair and a serious expression. \ No newline at end of file

616INDEX
Selaginellaaceae, 231.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 231, 232.Selaginella, 500,Spathulaea
SeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinaeSeleguinae