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MANNA er ** pietoke: it be se oek hehe OL. 24 - +6 #8 it. ?, * ot ’. on Pah’, o ve on ae ete re, ets ote S ##0hT00 TOEO O WIC 0 0 1OHM/18W TS ES ——— > aes <5 SRL he mo) Oo. a 2 -Q 2 gg » O me Ae Hn Ry oe an Q > ¥ YCETOZOA AND BACTERI DE BAR FUNGI * COMPARATI a M ondon HENRY FROWDE OXFORD UNIVERSITY PRESS WAREHOUSE AMEN CORNER, E.C, Clee §F3 . Pe (3 30 COMPARATIVE MORPHOLOGY AND BIOLOGY OF THE FUNGI MYCETOZOA AND BACTERIA BY A. DE “BARY PROFESSOR IN THE UNIVERSITY OF STRASSBURG THE AUTHORISED ENGLISH TRANSLATION BY HES@RY EE. Fs GARNSEY, M.A. Fellow of Magdalen College, Oxford REVISED BY ISAAC BAYLEY BALFOUR, M.A,, M.D, Fira, Fellow of Magdalen College, and Sherardian Professor of Botany in the University of Oxford WITH 198 WOODCUTS Oxford AT THE CLARENDON PRESS 1887 [ All rights reserved | PREFACE TO THE ENGLISH EDITION. * I po not deem it necessary to say anything in explanation of the reasons which have led to the preparation of this translation of Professor de Bary’s book on the morphology and biology of Fungi, Mycetozoa and Bacteria. It brings within reach of all English-speaking students the most thorough and comprehensive treatise upon these groups which has appeared in any language ; and the picture that is presented of the state of our knowledge of the subject at this time, along with the suggestions and indications of the lines upon which further investigation is especially wanted, will, it is to be hoped, not only instruct readers, but also stimulate them to research. To render adequately some of the precise terminology has been a serious difficulty in the translation. The terms which have been adopted are consistently used, and the occasional notes, along with the ‘ Explanation of Terms’ which I have added, should prevent all misconception of their signification. It must be remembered that the definitions and synonymy given at the end of the book have reference to terms only as they are used in the text; they are not exhaustive. The extension of the original meaning of Berkeley’s term ‘ sporophore’ and its use as the equivalent of - the German ‘Fruchttrager’ is a prominent innovation to which attention may be directed in this place. Several friends have been so kind as to give me their opinion and criticism upon questions of terminology, and I have specially to acknowledge suggestions from Professor Bower, Mr. A. W. Bennett, Dr. S. H. Vines, and Professor Marshall Ward ; for help in some difficulties I have to thank the author himself. I. B. B. OxFoRD: March 1, 1887, PREFACE, 5 * I puBiisHED a work in the year 1866 entitled Morphology and Physiology of the Fungi, Lichens and Myxomycetes as the second volume of Hofmeister’s Handbook of Physiological Botany. This work was intended to give a systematic and critical account of the state of our knowledge of the portions of natural history indicated by the title at that time. It had its mistakes and its deficie ; the index too was omitted, but for this I was. not responsible. At the same time it was not without its value; it paved the way for further advances and was favourably received. Some years ago I was urged by many persons to prepare a new edition of my work. Other occupations and duties long prevented me from setting about this task and interrupted and delayed it repeatedly after it had been begun; and when I addressed myself more closely to the work some four years ago, it soon became apparent that a new edition in the strict sense of the word would not satisfy modern requirements. Hence the progress of the work resulted in the production of a new book, which can only be partially regarded as a new edition of the earlier one, though this for brevity’s sake is always cited in the present work as the first edition, The reasons for the change had their origin in the considerable additions to the material to be discussed. Eighteen years ago it was comparatively easy to give a detailed description of the state of our knowledge of the morphology and physiology of the Fungi within a moderate compass. Since that time the amount of matter has increased greatly, and with it the number of questions and controverted points which have to be considered; an account which is not to be confined within the narrow limits of a text-book readily assumes large proportions and renders division of labour desirable. The physiology of the Fungi has received more comprehensive treatment than the morphology, partly in general treatises on vegetable physiology, those especially of Sachs and Pfeffer, and partly in the extensive modern literature of the chemistry of fermentation. There is no recent detailed critical survey of their morphology; in giving such a survey in the following pages, with brief allusions only to strictly physiological topics, I believe that I shall best meet both present requirements and the wishes of most of my readers. No comprehensive account of the morphology of any portion of the vegetable kingdom, and least of all of the Fungi, can be satisfactory without constant reference to the phenomena known as biological, that is to their habits of life and adaptations. Viii PREFACE. These must therefore be handled at some length, and in their turn again lead up to the consideration of questions of physiology. I ought perhaps to have carried the change still farther, and have omitted a variety of anatomical and histological details, the introduction of which was suitable and necessary eighteen years ago, but which in the present state of botanical science may be regarded as superfluous or at least not indispensable. Still they can do no harm, and may possibly or even probably be of service. I have therefore taken some matter of this kind from my former work, and added it to the main text of the present publication in the smaller type employed for the description of some other details, One change which I have ventured to introduce may and perhaps will be objected to. It is, that I have omitted the section which treated of the origin of the Fungi, Myxomycetes and Bacteria, and that I set out in all cases from the assumption that these plants are like all other plants the product of germs, each of which is derived from parents of the same species and owes its existence in every species to processes of development in the parents or to organs belonging to them. It is known that other views have prevailed with regard to the origin of the plants described in this work, and are still entertained by a few persons. It may be observed in passing that the early botanists, of whom mention is made in Ehrenberg’s Epistola de Mycetogenesi, considered the Fungi to be merely lusus naturae and no plants at all. There are some who still think that Fungi and Bacteria are certainly plants, but that they are or may be produced by spontaneous or heteromorphous generation (abiogenesis, heterogeny), that is from inorganic matter showing only chemical predisposition to organisation, like crystals in the mother-lye, or else from commencements which are organised but which proceed from organisms that are not themselves either Fungi or Bacteria. The former of these two views requires no further consideration in this place. The other will be discussed in Chapter V, p. 270, in the special case of Sprouting Fungi and Yeast-fungi; it assumes in general terms, that constituent portions of living cells belonging to higher organisms, ‘vesicles, granules,’ the microsomata of modern terminology, can continue an independent life after the death of the living body of which they formed a part, and develope under favourable conditions into Fungi and Bacteria. These forms may then develope their specific germs, and a progeny from these germs specifically resembling the parents. H. Karsten and his adherents represent views of this kind, and A. Wigand has supported them at the present day. Their most logical development is to be found in A. Béchamp’s theory of the micro- zymes. These are very minute bodies, ‘granulations moléculaires,’ which are contained in the substance (protoplasm) of animals and plants of the most different kinds and grades of organisation, and not only develope independently after the death of the parent-organism, but enjoy an almost unlimited duration of vitality, since they may lie during entire geologic periods in such a rock as chalk, and yet retain the power of development. These microzymes give rise in a suitable medium to Bacteria, Sprouting Fungi, and similar forms, and since the localities in which they originate are of very frequent occurrence they are to be found everywhere. Béchamp published his theory in the Reports of the Academy of Paris twenty years ago; he reproduced it in the Transactions of the Medical Congress at London in 1881, and PREFACE. ix in a large new work, Les Microzymas dans leurs rapports avec l’hétérogénie, l’histio- génie, la physiologie et la pathologie, Paris, 1883. Theories of the kind here described, and others more or less like them, are constantly recurring from time to time on the subject of the origin of the Fungi and Bacteria. They appeared in earlier times with still greater breadth of application. Fifty years ago it was believed that not only minute organisms but that Fungi of the size of the Uredineae were produced from the altered substance of other organisms, in the case of the Uredineae from phanerogamous plants; two hundred years ago maggots were supposed to be bred from putrid flesh. It is easy to understand how such ideas of spontaneous generation should have been prevalent in ancient times. Even their repeated recurrence in modern times and with our modern know- ledge is also capable of explanation. It must be assumed that organisms did once come into being of themselves without parents, being produced from organisable but not yet organised matter. It must moreover be allowed, that this may still happen at any moment and perhaps does actually happen; its impossibility cannot be proved. To produce actual proof of an original formation of a living being is a matter of the highest interest, and has as powerful attraction for the biological investigator, as the prospect of producing the homunculus in the phial for the alchemist. But the experience of centuries has shown that whenever the homunculus really appeared in the flask, it proved to be a small imp which had been secretly introduced into it from without ; and speaking seriously, the result was always of this kind. In every single instance exact investigation has shown that the organisms which were supposed to have had no parents proceeded from germs produced from parents of the same species as themselves; it has also shown how they were formed and whence they came. Those who maintained that direct proof had been given of generation without parents have been driven back step by step into narrower territory, and upon minuter and at last upon the minutest objects, from simple inorganic matter to the organised mini- mum, the ‘atome structuré vivant’; in other words they were reduced to seek their proof where it is still most difficult to say whether it is to be found or not. This is what has happened in all researches into the origin of the Fungi, as soon as each individual case was rigidly examined. We have had ocular demonstration of the fact since the year 1860, through the labours especially of Pasteur and his school. That there is no generation without parents is therefore a maxim of experience; it is in distinct accord with the present state of our knowledge, after making allowance for all conceivable possibilities, and we must set out from this principle in a book which is concerned with real knowledge. There is not much to be said by way of preface with regard to the plan of this work. I have endeavoured to make my remarks intelligible even to those who are only beginning the study of the Fungi, but I have assumed that my readers are masters of such a previous general knowledge of botanical science as is to be obtained by a course of study in a University, or by the use of good text-books. The reader is here referred to such works, especially to Sachs’ Text-book and Lectures, and Goebel’s Outlines, and also to Prantl’s and Luerssen’s smaller compendia, and among works not in German to Van Tieghem’s Traité de Botanique. A few descriptions only of individual Fungi will be found scattered through the volume ; others must be sought in our at present imperfect floras, in Saccardo’s dea PREFACE. Sylloge Fungorum for example, in Winter's Die Pilze Deutschlands, P. A. Karsten’s Mycologia Fennica, and Fries’ more important publications, which latter must always be indispensable; books also of descriptive lichenology must be consulted. The new edition of Leunis’ Synopsis by A. B. Frank, and in its special line Frank’s Pflan- zenpathologie, are works to be recommended to the student. I must not be supposed to express an unfavourable opinion of other works because I do not mention them; my only purpose is to point out some books which will be of service to those who require direction in their reading. I have endeavoured to make myself as well acquainted as was possible with the special literature of my subject and to draw it into my service. I have made some use even of publications which appeared at the close of the year 1883 and the beginning of 1884 while my book was being printed. That some particulars have been omitted altogether, or been forgotten for the moment in the preparation of some of the sections, is what I should have expected beforehand, even if I had not subse tly noticed their omission. I must plead in excuse the extraordinarily large number of mycological communications of every possible size which have been published during the last twenty years. The number of publications on the Fungi is so large that it was impossible to quote them all, and to have done so would have transgressed the limits of practical utility. The more important references given in the text will in every case show where further details are to be obtained, especially with the assistance of Hoffmann’s Mycologische Berichte from 1865 to 1872, and Just’s Jahresbericht, which has appeared regularly since 1873. Special notices of the literature of the subject will be found in the separate sections of the work. The illustrations are for the most part the same as those in the earlier work. A certain number are new and drawn by myself; a smaller portion have been taken from other authors whose names are in every case given in the explanations appended to the figures. I express my warmest thanks for the permission to use these illustrations, and no less warm thanks to all those who have lightened my labours by their communications and by assistance of other kinds. e A. pe BARY. STRASSBURG: /une 30, 1884. SECTION I. II. III. IV. XV. XVI. TABLE OF CONTENTS. FIRST PART. FUNGI. DIVISION I. GENERAL MORPHOLOGY. CHAPTER I. HiIsToLocicaL CHARACTERISTICS. General construction. Hyphae. Growth-forms: Filamentous Fungi, Fungus-bodies, Sprouting Fungi (Chytridieae, Laboulbenieae) Structure of Fungus-cells : Protoplasm, Cell-nuclei, Cell-contents Cell-membrane: Structure, Material composition, Excretion of calcium oxalate . Remarks. Literature . CHAPTER II. DIFFERENTIATION OF THE THALLUS. 1. General Survey. Mycelium and sporophore ; ; 2. Mycelium. Mycelia. Filamentous mycelium. Haustoria Mycelial membranes Mycelial strands (Rhizomorphae, reare pi Weass) Sclerotia : Structure, origin, germination Details. Historical remarks ‘ : : Sclerotioid bodies: Transitory resting states: Xyloma Literature ‘ : 3 : 3. Sporophore. General characteristics Simple sporophores ‘ ea ; ‘ ; ‘ : Compound sporophores. General differentiation. Course of growth. Structure of mature compound sporophore . CHAPTER III. Spores or Funct. Introduction. General characteristics and distinctions I. Development and Scattering of Spores. General phenomena of development . ° ° : ° : . Intercalary and acrogenous spore-formation. Basidia. Sterigmata . AGE 17 18 21 22 30 40 42 43 45 46 48 57 59 6c 61 xii CONTENTS. SECTION XVII. Dissemination of acrogenously formed spores. Abscision. Abjection. Disappearance of the sporiferous structure. . . : ste XVIII. Endogenous spore-formation : (a) Sporangia of Phycomycetes ‘XIX. (6) Asci. . cae ee panes ak Se ae XX. Dissemination of cease érmed spores : (a) Phycomycetes ;: ‘ ° . 4 ° : : . XXI. (4) Ascogenetic spores. Ejection. Mechanical arrangement for ejection of spores. Simultaneous and successive ejection. Mechanism of simultaneous ejection XXII. Puffing in Discomycetes : ; XXIII. Peculiar mode of ejection in Pyrenomycetes . XXIV. Force of ejection : XXV. Reported peculiarities in £iniocis each XXVI. Successive ejection from asci . XXVII. Solution and swelling of asci . ; XXVIII. Maturation of ascospores after ejection . : XXIX. Combinations of different kinds of St i eA ; sporidesms II. Structure of ripe Spores. XXX. Spore-membrane. Exosporium, episporium, endosporium. Germ- pores. Gelatinous envelopes and appendages.—Protoplasm, nucleus, content.—Swarm-spores . . . A ° ‘ . . ° III. Germination of Spores. XXXI. Tube-germination and sprout-germination—Germ-tube. Primordium of the mycelium. Promycelium and sporidia Historical remarks on Chapter III . : . . : ° . PAGE 109 115" DIVISION II. COURSE OF DEVELOPMENT OF FUNGI. CHAPTER IV. Inrropvucrion. XXXII. General course of development in Algae, Mosses, Ferns, and Phanero- gams. Homologies and affinities. Form-genera and form-species in Fungi. Tulasne’s pleomorphy. Gradual recognition of the course of development and of the homologies in Fungi. Main or Ascomycetous and other series . . . . . . . . XXXIII. Closer consideration of the course of development of the higher plants. Archicarp; fructification.—Spore, sporocarp, sporophyte.— Sexual and asexual segment of the development. Homology of a member of the development independent of its sexual function. Interruption and restoration of the homologies.—Alternation of generations.—Homology interrupted and not restored . XXXIV. Agreement of the course of development of the Fungi with that of plants which are not Fungi. Meaning of penne Misunder- standings and the way to remove them . ‘ : . 119 12! 126 CONTENTS. xiii SECTION PAGE XXXV. Terminology. Spores. Gonidia, &c. 128 XXXVI. Review of the chief groups of Fungi _132 CHAPTER V. CoMPARATIVE REVIEW OF THE SEVERAL GROUPS. Peronosporeae. XXXVII. 132 Ancylisteae. XXXVIII. ‘ - : 3 : ; : : : e 4 F a: x 539 Monoblepharis. XXXIX. 140 Saprolegnieae. XL. 141 Mucorini. XLI. General course of development 145 XLII. Zygospores. (a) Mucoreae and Cinstocladitad ) Piptocephalideae— Azygospores . . . 147 XLIII. Typical gonidiophores. inusaiean SC hechoctadieas: —Piptocephais and Syncephalis , Patt 61 XLIV. Accessory gonidia. Acwogeibia (ctidiniptoaneres, stsleabieeeny Choanephora.—Gemmae.—Serial gemmae, sprout-gemmae 154 Doubtful Mucorini. Historical remarks. Literature 156 Entomophthoreae. XLV. 158 Chytridieae. XLVI. Common characteristics of the present group of Chytridieae. Spor- angia. Resting spores . ‘ , ; S'S XLVII. Rhizidieae.—Polyphagus. Less well known forms 162 XLVIII. Cladochytrieae 165 XLIX. Olpidieae 166 L. Synchytrieae 167 LI. Comparative review ; ‘ ; ‘ , ' 169 LII. Doubtful Chytridieae. Tetrachytrium. Hapalocystis 170 Literature ‘ ‘ r 171 Protomyces and Ustilagineae. LIII. Protomyces . ‘ . . . . ‘ - 171 LIV. Ustilagineae. Conformation. Compound sporophore 172 LV. Development of resting spores . s ‘ 174 LVI. Structure and germination of resting spores ‘ ‘ 176 LVII. Gonidia of Tuburcinia and Entyloma , ‘ 179 LVIII. Course of development and homologies 180 xiv SECTION LIX. LX. LXI. LXII. LXIII. LXIV. LXV. LXVI. LXVII. LXVIII. LXIX. xx. LXXI. LXXII. CONTENTS. Ascomycetes. GENERAL CHARACTERS. SPOROCARPS. Structure of sporocarp. Apothecium, perithecium, cleistocarp Apothecia Perithecia Cleistocarpous Siseas eh phonietes —Tuberaeals —Onygena Myr angium . Petite mite 6 ke ‘ : : ORIGIN OF SPOROCARP. Review of the main facts. 1. Eremascus.—2. Genera which have at first a distinct archicarp with no distinct envelope.—3. Polystigma with archicarp in the primordium of the sporocarp.—4. Xylaria and allies with a temporary Woronin’s hypha.—Genera without a distinct archicarp Separate descriptions. . Erysipheae . Eurotium . . Penicillium é ; . Gymnoascus. Ctenomyces . Ascobolus . Pyronema ; . Sordaria. Melisespeca ’ . Collemaceae . Forms with archicarp snweshaiily emnihtied . Polystigma 11. Xylarieae 12. Sclerotinieae 13. Pleospora herbarum 14. Claviceps, Epichloe, a Net ectria and occ 15. Ascodesmis 16. Sphyridium, ay Cladonia ae piers oo on An fhW DN Early investigations into the development of the sporocarp in Lichens . THE COURSE OF DEVELOPMENT IN ASCOMYCETES. Statement of facts. Species without gonidia; others with a regularly intercalated formation of gonidia. Different forms of gonidia in the same species. Microgonidia and megalogonidia. Pycnidia, pycno- spores, stylospores.— agian of species which have been fully examined Homologies of the sided of ‘the devise in Ascomycetes. Controversy regarding the sexual organs DETERMINATION OF IMPERFECTLY KNOWN ASCOMYCETES. The points on which the question turns Archicarps, sporocarps ‘ Spermogonia and spermatia . . ; ; : ; fy. Doubtful spermatia Gonidia, gonidiophores, pycdiidia ; : F Combinations of different forms. Examples of the kind PAGE 185 187 190 193 197 201 203 204 206 206 208 210 211 214 215 216 218 220 220 221 221 222 223 231 238 239 240 242 244 248 SECTION LXXIIl. LXXIV. LXXV. LXXVI. LXXVII. LXXVIII. LXXIX. LXXX. LXXXI. LXXXII. LXXXIII. LXXXIV. LXXXV. LXXXVI. LXXXVII. LXXXVIII. LXXXIX. XC. XCI. XCII. XCIIl. XCIV. CONTENTS. Occurrence of known or supposed members of the development of some species outside thenormal connection. Tendency of these to constantly similar production. Hence a pee reduction or splitting of a species : ‘ Determination of organs of propagation which se rae Pa Ee to be rudimentary . ; Literature of sections LIX—LXXIV. DOUBTFUL ASCOMYCETES. Introduction. Laboulbenieae . Exoascus Saccharomyces . Affinity between Exoascus and a ahaddinesés of the latter group to the Ascomycetes . Confusion between the ‘ Yeast-plants’ Literature . Helicosporangium. Papulaspora. Possible relations Uredineae. Aecidia-forming and Tremelloid Uredineae. Sporocarps (aecidia) and spermogonia of the aecidia-forming eS Course of de- velopment of Endophyllum ‘ , ' , Aecidia-forming Uredineae with gonidia : sepsiebaien: uredo . Uredineae with imperfectly known course of development Tremelloid Uredineae . ‘ Relationship between sien and hibeocinbite Literature . Basidiomycetes. Introduction : : HYMENOMYCETES. Conformation of unveiled sporophore Veiled sporophore. Velum. Annulus. Volva Structure of full-grown sporophore Hymenium. Cystidia. Basidia GASTROMYCETES. Comparative account of the differentiation of the sporophore Special morphology, history of development and anatomy of the same ‘ Y ; COURSE OF DEVELOPMENT AND AFFINITIES OF BASIDIOMYCETES. Course of development of perfectly known form. Exobasidium, Tremellineae, Typhula, Coprinus, Agaricus ee Crucibulum and Cyathus, Sphaerobolus ; : P Gonidia of Basidiomycetes which have been shoepaehly scenitnad : Imperfectly known and doubtful gonidia Homologies and affinities of Basidiomycetes Literature . ° xXV PAGE 251 255 261 263 265 267 269 270 272 274 279 282 283. 285 285 286 287 289 297 300 308 312 328 331 333 337 341 Xvi CONTENTS. DIVISION III. MODE OF LIFE OF FUNGI. CHAPTER VI. PHENOMENA OF GERMINATION. 1. Capacity of germination and power of resistance in Spores. SECTION XCV. Duration of capacity of germination in spores. Resting state. Power of resistance to mechanical injuries, withdrawal of water, extreme temperatures 2. External conditions of germination. SGV Is =. ; ; “ Ss 4 h . ‘ . : . : CHAPTER VII. PHENOMENA OF VEGETATION. 1. General conditions and phenomena, XCVII. Conditions affecting growth. Temperature . . : . : XCVIII. Nutrient substances. Other chemical constituents of the Satins. Effects of Fungi on the substratum. Fermentations, oxidations. Ferment-excretion ‘ : ' a ‘ “ . . . ° 2. Nutritive adaptation. XCIX. Distinction of 1. pure saprophytes, 2. facultative parasites, 3. obligate parasites either a, strictly obligate, or 4, facultative saprophytes ° 3. Saprophytes. 4. Parasites. CI. Adaptation between parasite and host. Predisposition of host. Endo- phytic and epiphytic parasites . . Mae Yan. os ne CII. Attack of parasite on host ‘ > ° . : CIII. Growth of parasite after it has seized on the host and reactions of the host on the parasite. Destroying and transforming parasites PARASITES ON ANIMALS. CIV. Facultatively parasitic Aspergilli and Mucoreae; obligately parasitic Entomophthoreae, Laboulbenieae, Cordyceps, Botrytis Bassii CV. Imperfectly known parasites on animals : Saprolegnieae CVI. Fungi of skin-diseases . ° * a ‘ ‘ CVII. Actinomyces. ‘ Chionyphe Carteri’ . ‘ . ‘ PARASITES ON PLANTS. a. Facultative parasites. CVIII. Fungi of rotting fruit. Sclerotinieae. Pythieae. Nectriae. Hartig’s wood- destroying Hymenomycetes ° . ° . . . ‘ PAGE 343 349 352 353 356 357 358 360 366 369 375 376 377 379 SECTION CIX. CX. CxXI. CXII. CXIII. CXIV. CXV. CXVI. CXVII. CONTENTS, b, Obligate parasites. Facultatively saprophytic : Peronosporeae, Mucorini, Ustilagineae, Exo- basidium, Myxomycetes ; sicily obligate : Peronosporeae, Erysi- Dheae Uveduieee. Gee ie en Autoecism and metoecism . 2 ; Growth and extension of parasites in substance of tees sae Behaviour of these parasites to separate tissues and to the parts of the cells of the host . ; ° . Reactions of the plants stacked Lichen-forming Fungi. Formation of the Lichen-thallus by the growing together of certain Algae and Ascomycetes and a few Hymenomycetes which attack them. Enu- meration of Lichen-forming algal forms as at presentknown . First beginning of the Lichen-thallus. ‘ P ; fogs , Conformation and structure of the Lichen-thallus. Fruticose, foliaceous and crustaceous forms. Distinctions in anatomical structure: 1. Heteromerous thallus. 2. Graphideae and similar forms. 3. Granular crustaceous thallus of Thelidium and others. 4. Coenogonium-form. ‘ 5. Collemaceae or Gelatinous Lichens, 6. Hymenomycetous Lichens Soredia ‘ ‘ * ‘ Pseudo-lichens, oPeiashaden| suai: Literature , ; i SECOND PART. MYCETOZOA. CHAPTER VIII. Morpnotocy AND Coursk oF DEVELOPMENT: CXVIII. CXIX. CXX. CXXI. “CXXII. CXXIII. CXXIV. " Myxomycetes. Spores. Germination. Swarm-cells Plasmodia ‘é . : : ; : : Transitory resting states. Cysts. Sclerotia . Development of sporophores and sporangia . ° : Structure of mature sporophores and sporangia ; ie vonbewen of Cera- tieae ; simple sporangia ; aethalia ‘ . . “ ° . Acrasieae. Affinities of the Mycetozoa, Doubtful Mycetozoa. CXXV. Bursulla. Vampyrellae. Nuclearia. Plasmodiophora [4] b xvii PAGE 385 386 389 392 394 395 421 423 427 429 434 441 442 446 XViili CONTENTS. CHAPTER IX. MobpDe or LIFE OF MyYCETOZzOA. SECTION ‘PAGE CXXVI. Conditions of germination . : : ° . : : : - 448 CXXVII. Phenomena and conditions of vegetation. Causes of movement of plasmodia. Enclosing of solid bodies. : 2 ; : - 449 CXXVIII. Process of nutrition . . . : ‘ aici eee : on a Literature. ee ; : " oS pigeeue ior pen | THIRD PART. BACTERIA OR SCHIZOMYCETES. CHAPTER X. Morpuo.iocy or BACTERIA. CXXIX. Structure of cells, Cell-aggregates and growth-forms . “ Se CXXX. Course of development. Endosporous and arthrosporous forms. De- velopment of endospores. Special description of some Bacilli . 459 CXXXI. Development of arthrosporous forms . . ‘ ‘ . ANE CXXXII. Controversy respecting species in Bacteria . es: - 472 CXXXIII. Systematic position of Bacteria . . 3 ora ‘ . a’ 674 CHAPTER XI. Mobs or LIFE oF BACTERIA. CXXXIV. Capacity and conditions of germination in spores : ee - 476 CXXXV. General conditions and phenomena of vegetation.—Temperature. Nutrient substances. Oxygen. Aerobia, and anaerobia. Effect - of substances not serving as nutrients, Oxygen and nutrient sub- stances as inciters of movement " ; ° . ° . - 478 CXXXVI. Special vital adaptations. Saprophytes. Parasites. Parasites on plants. Parasites on animals. Exciting causes of disease. Life- history of Bacillus Anthracis as an example of facultative parasites. Doubtful obligate parasites; Spirochaete Obermeyeri; Nosema ‘Bombycis.—General remarks on Bacteria which excite disease . 481 Literature. : 3 : 4 ; ; ‘ - ; . . 489 EXPLANATION OF TERMS ‘ ‘ . - 5 4 ; ; ° ; o> Qn Inpex ow. ka, eee Lee — ERRATA. Page 1, line 15, for rudimentary branch vead branch-primordium. ”? 9, line 8 from bottom, for Muscaria read muscaria. » line 3 from bottom, for erinaceus read Erinaceus. 18, line 2, for or read and. 29, lines 1 and 8, for fructification ead sporophore. 34, line 5 from bottom, for commencemet vead commencement. 50, line 5 from bottom, for Coprineae read Coprini. 51, line 4, after Clavarieae insert Calocera. » line 15 from bottom, for Coprineae read Coprini. 57, line 16 from bottom, for Helvetia’ read Helvella. 64, line 22, after sterigma read , as in Coprinus. 76, line 12, for orientated read originated. 99, line 5, for sporiderms read sporidesms. 130, line 4 from bottom, for rudimentary read commencing. 162, line 5 from bottom, for tubular-rhizoid processes, read tubular rhizoid- processes. 177, line 4 from bottom, for sometines read sometimes. 181, line 7, for Urocystis read Ustilago. 192, line 6 from bottom, for Verrucariae read Verrucaria. 244, last line, for polytrichum vead polytricha. 268, line 3, for Mycodermain, vead Mycoderma in. 277, line 7 from bottom, for sempervivi read Sempervivi. 286, last line, for 53 read 48. 306, line 14, for violacea read foliacea. 330, line 12, for 25°C. read 25°C. 349, line 9, for winter, of read winter of. 352, note 2, for 294 read 262. 368, lines 25 and 26, for fir read silver-fir. 376, line 17, for Mentagrophytes, Rob.; ead Mentagrophytes, Rob.) ; », line 18, for pityriasis versicolor). read pityriasis versicolor’. 391, line 2 from bottom, for hypodites read hypodytes. 399, line 8 from bottom, for peridermis vead periderm. 406, line 16 from bottom, for malacca vead malacea. 427, line 18, for Stemonites vead Stemonitis. 428, line 5 from bottom, for homogenous vead homogeneous. 434, lines 18 and 19, for serpula read Serpula. 441, line’ 17 from bottom, for serpula vead Serpula. First ~ PART: FUNGI. DIVISION I. GENERAL MORPHOLOGY. CHAPTER I. HISTOLOGICAL CHARACTERISTICS. Sxction I. The thallus, which in most Fungi is the whole body of the plant not serving directly as an organ of reproduction, begins as a tubular germ-cell (germ-iube, Keimschlauch) which, by continued growth progressing in an apical direction accompanied by repeated formation of lateral branches, developes into a branched body of cylindric- thread-like form, the Aypha. Both growth and branching follow the laws which prevail generally in the vegetable kingdom. The branching is usually monopodial, in a few cases only it is dichotomous, as in Botryosporium, species of Peronospora, and some Mucorini. In some groups, especially the Saprolegnieae, Peronosporeae and the Zygo- mycetes, the thallus or hypha of the Fungus, like the thallus of the Siphoneae, is an unsegmented branched tubular cell up to the time when organs of reproduction are formed. But in the great majority of cases it becomes a branched row of cells owing to the incessant formation of transverse walls concurrently with the growth of the hypha at its apex. ‘The segmentation either takes place only in the apical cell for the time being and at the place of insertion of the rudimentary branch, so that each branch is made up of an apical cell and segment-cells of the first order only, as in Penicillium’ and Botrytis cinerea, or new intercalary partition-walls are formed in the segment-cells of the first order. In the more simple Fungi the branched hypha alone constitutes the thallus; such forms are termed Hyphomycetes, /2/amentous Fungi (Fadenpilze), or Haplomycetes*. The body of the largest Fungi, the Mushrooms and Lichens of ordinary parlance, are also composed of hyphae, but their ramifications meet and cohere to form larger aggregates. Such a body, which appears as if formed by the union of Filamentous Fungi, may be termed a compound Fungus-body (zusam- ! Low in Pringsheim’s Jahrb. VII. p. 473.—Brefeld, Schimmelpilze, II. p. 27. * From the Greek word dmAods, meaning simple. “ k [4] B 2 DIVISION I,—-GENERAL MORPHOLOGY, mengesetzer Pilzkérper) or simply a Fungus-body to distinguish it from that of the simple Filamentous Fungus. Both are grow/h-forms (Wuchsformen) comparable with those growth-forms in the higher plants which are known as the tree, shrub, and herb. Many species appear only in the filamentous form, as succeeding chapters will show; others assume both forms according to their stage of develop- ment and external conditions ; all have the filamentous form in their earliest stage. It is obvious that intermediate forms will be found between these two chief ones. It has been assumed above that a hypha or a Filamentous Fungus is the product of a single germ-cell, and this is often actually the case. It has been repeatedly shown that even a compound Fungus-body may be composed of the ramifications - of a single filament proceeding from a single germ-cell. But this is not always - the case, or at least cannot always be proved, owing to the frequent coalescence, of similar hyphal branches with one another (Fig. 1), which takes place in the a FIG. 1, Germinating gonidia of Nectria (Spicaria) Solant, FIG. 2. Clamp-connections of the my- Reinke ; a developing into an isolated hypha, in the rest the celium of Hypochnus centrifugus, Tul hyphae have coalesced. Magn. 390 times. Magn. 390 times. following manner :—the lateral wall or the extremity of a branch or of a segment- cell of the branch places itself on another branch or cell, and the membranes of both disappear at the point of contact, so that the cavities and protoplasmic contents of the two cells become united into one. Coalescence in this way may take place between the branches of the same hypha, and also between such as are growing together but were originally distinct, being the product of distinct germ-cells. The forms which result from such coalescence are very various ; H-shaped cross links or bridges, loops of various form and number, even network of many narrow meshes are found. One curious form must be mentioned here, the c/amp-connections (Schnallen- verbindungen), first observed by Hoffmann (Fig. 2). They occur only on hyphae with transverse segmentation, and chiefly in the Basidiomycetes (many Agaricineae, species of Polyporus, Typhula, Hypochnus, Cyathus, Hymenogaster, &c.). A clamp of this kind when fully formed is usually a nearly semicircular protuberance like a short branch which springs from one cell close to a transverse wall, and‘is closely applied to the lateral wall of the adjoining cell in such a way that the transverse wall cuts the middle of the plane of contact at a right angle. Sometimes the protuberance does not lie close on the lateral wall at all points, but forms an eye-hole. Brefeld observed the origin of these formations in Coprinus, and found that the protuberance extends. itself from the one of the two adjoining cells to the other, and then coalescence takes place, so that the two cells enter into open communication with CHAPTER I,—HISTOLOGICAL CHARACTERISTICS. 3 one another through the protuberance, and finally the protuberance is separated from the cell on which it first arose by a new wall which usually coincides with the plane of the lateral wall. The protuberance generally continues in open communication with the second cell, with which it coalesced; but here too subsequent separation is sometimes, though seldom, effected by the formation of a wall, and it is only to this exceptional case that Hoffmann’s original term ‘ clamp-cells’ is properly suited. In Coprinus. according to Brefeld the first cell, the cell which puts out the protuberance, is always the one on the apical side of the transverse wall. In this case therefore the whole structure is formed almost exactly in the reverse way to that which is suggested by its appearance when fully formed; whether this is -so in all other cases has yet to be ascertained. « The growth of the compound Fungus-body, so far as it depends on the formation of new cells and not on the expansion of the old, is due simply to the growth in length of the united hyphae and to the formation of new branches on them; these branches are formed partly on the surface of the body, partly in its interior, where they thrust themselves in between the branches previously formed. In the fully developed state of these compound forms it is in most cases easy to see the fine fibrillation due to their construction out of hyphae; the course of single hyphae and their ramifications may often be followed with the aid of the microscope for considerable distances, whether they lie parallel. to one another or whether they cross one another repeatedly and are intertwined. In other cases the entire thallus or separate parts of it appear to have an entirely different composition. Here the tissue when fully formed consists of isodiametric roundish or polyhedral cells, and especially in thin sections no longer appears to be an arrangement of hyphae, but resembles the ordinary parenchyma of the higher plants. Examples of this tissue are to be found in the pileus of Russula and of Lactarius, in the rind of the peridium in many of the Lycoperdaceae, in many sclerotia, in the stipe of the Phalloideae, in many Lichens, and in some other cases. But if we examine this tissue more closely and follow the history of its development, we see plainly that it is really formed from and consists of hyphae, and that it owes its parenchy- matous structure simply to the firm union of the hyphae, and to the form, expansion, and displacement of their cells. The parenchyma of the higher plants is formed by cell-division, the partition-walls as they successively arise being placed in turns in one of three or two directions in space. From this difference in origin the Fungus- tissue of which we have been speaking is distinguished by the name of pseudo-parenchyma. Successive cell-divisions in two or three directions occur only exceptionally in the formation of the thallus of the Fungi, as in pycnidia and perithecia (on this see Division II). — The union (Verbindung) of the hyphae to form the compound Fungus-body is for the most part brought about by their zw/rweaving (Verflechtung) one with another, _and the direction and closeness of the weft vary according to the species. The hyphae of the flocky felt-like tissue of Polyporus fomentarius’, of Daedalea, of the stipe and pileus of the Amaniteae, of the medullary layers of many Lichens, &c. are loosely woven, leaving broad interstices usually filled with air; those of the firm tissue, often * Amadou of commerce.. B 2 4 DIVISION I.—GENERAL MORPHOLOGY. hard as horn or wood, in the dark rind of the dry Pyrenomycetes, of the Tuberaceae, of many sclerotia, &c., leave scarcely any intercellular spaces. Every intermediate stage is to be found between the loose accidental intertwining of the socially growing Hyphomy- cetes and the firm structure of the Fungi which have a definite form, and states the farthest apart from one another sometimes occur in the same species. When the hyphae run parallel to one another, as in the stipe of Agaricus Mycena, Coprinus and other species, their connection may be brought about by cementation (Verklebung) or concrescence (Verwachsung) of the membranes, and in the same way they often gain much firmness where they are interwoven with one another. In hard tissues, as the rind of many non-fleshy Fungi, and in the masses of gelatinous tissue described on page 9g, the outer surfaces of the hyphae are often inseparably grown together, or are cemented together by a narrow slip of a firm homogeneous substance ;, in fleshy Fungi the hyphae are often united by an intervening substance which softens in water and allows them to be artificially separated. This cementing substance may be called zwtercellular substance. Whether it is to be regarded as a part of the cell-membranes themselves or as an entirely distinct body from them, is a question which in the case of the Fungi has not yet been specially examined ; there is therefore the less ground for assuming other laws than those which prevail in the histology of other plants. Lastly, the coalescence above mentioned of branches originally distinct also adds to the firmness and solidity of the compound Fungus-body ; its occurrence is shown in fleshy and gelatinous species by the frequency of H-shaped connections, though no special researches have been made into their mode of formation. Of the exceptional cases referred to above in which the Fungus-thallus is not formed of hyphae, the first to be noticed is that of the forms recently termed by a @2Q % 23 Nageli Sprouting Fungi (Sprosspilze). This name, like that of Filamentous Fungi, indi- @ cates a growth-form; and this is the only form in some Fungi, as in the species of os LC the genus Saccharomyces known as Yeast- e fungi, or it is peculiar to particular states of “ey other species which otherwise appear as fila- iri mentous or compound forms. In the latter Fic. 3. Saccharomyces Cerevisiae; a cells before CSS it may be a matter of doubt, for reasons Fa ecco eatin the nee oy ac eaun® to be hereafter discussed, whether the sprout atest ae is to be regarded as a vegetative or as a reproductive organ, The characteristic features of the Sprouting Fungi are as follows (Fig. 3). A cell grows to a certain size and shape, the latter being usually spherical or somewhat ovoid, and puts out an excrescence or sprout which remains connected with it by a narrow base; this new formation is of the same nature as the parent-cell and is separated from it by a transverse wall either before or after it has reached its proper size. The process of sprouting may be repeated in the daughter-cell and in every succeeding generation, the number of which is unlimited in presence of sufficient nutriment. The number of sprouts that can be produced by each active cell and the spots at which they appear are not certainly determined, though with regard to the CHAPTER I.—HISTOLOGICAL CHARACTERISTICS. 5 latter it is possible to give certain rules in individual cases; as a rule the sprouts may arise simultaneously at several spots in the mother-cell, or one after another from the same spot. If all the generations of sprouts continue united to one another, it is obvious that their combination simply forms an irregularly branched hypha, which is distinguished from ordinary segmented hyphae only by the constriction at the narrow point of insertion of the sprout-cells. . This is in fact the condition in which the cells remain as long as they are not disturbed; but eventually the full-grown sprouts separate easily from one another, and a slight movement leaves only isolated sprouts or small aggregates of them. The second exception is found in those simplest forms of the Chytridieae, in which the entire thallus consists of a single round cell which ultimately produces spores; the-less simple species of this group are allied by their structure to the unicellular Filamentous Fungi described in sections XLVI-L. The Laboulbenieae may perhaps be reckoned as a third exception, but their character is still very imperfectly known (see Division II). The view given above of the structure and growth of the thallus of the Fungi has been already distinctly indicated in Ehrenberg’s Epistola de Mycetogenesi (Nov. Act. Acad. Nat. Cur. X); it is also clearly expressed in Vittadini’s Monogr. Lycoperdineorum (Mém. Acad. Turin. Ser. II, V, p. 146, 1841); and the views of later writers (Montagne, Esquisse organographique, &c. sur les champignons, Paris, 1841, German edition, Prague, 1844, and Schleiden, Grundz. 3rd edition, II, p. 34) are in accordance with it. .Schleiden, and Unger after him (Anat. u. Physiol. d. Pflanzen, p.149),call the weft of distinct hyphae felted tissue, ‘ tela contexta.’ Thoroughly to establish and work out this view required fresh anatomical investigations, and to these Bonorden and Schacht have given the chief impulse and contributed the first more important materials. See Bonorden, Allgem. Mycologie, Stuttg. 1851, and Schacht, Die Pflanzenzelle, p. 134. : On the clamp-connections see Hoffmann in Bot. Ztg. 1856, p. 156; Tulasne, Carpol. I, 115; Bail in Hedwigia, I, 96, 98, &c.; Brefeld, Unters. iiber Schimmelpilze, III, especially p. 17; Eidam in Cohn’s Beitr. z. Biol. Bd. II, 229. The distinction of pseudo-parenchyma or apparent parenchyma was introduced by myself in the first edition of this work. The term may be retained as it has become familiar ; but it should be remembered, that it ought only to be used to indicate the appearance of the close short-celled tissue of the Fungus with reference to the ordinary conformation of the parenchyma of the higher plants. If the latter tissue is charac- terised not, as is most usual, by the form of its cells, but by their structure and by the functions indicated by their structure, then the pseudo-parenchyma is neither more nor less to be compared with it than any other aggregate of cells in the Fungus which serves for metabolism. The term Sprouting Fungus may be used as a general expression for the growth- form which it designates. As the Saccharomycete with this form of growth which has chiefly come under consideration is. yeast, the term Yeast-fungus has usually been employed instead of Sprouting Fungus ; but this leads to confusion, and the word Yeast- fungus should not be used for the growth-form, but should be confined to the special cases to which it is suited. The Schizomycetes will be described in the third part of this work. Section II. The cells of the Fungi agree in all important points with the cells of other plants as regards structure, growth, and mode of division. The protoplasm, which in most cases fills uninterruptedly the interior of the young cell, encloses in the full-grown cell of the Fungi; as of other plants, one or _ 6 DIVISION I,—GENERAL MORPHOLOGY, several sap-cavities (vacuoles). Comparatively large vacuoles are often separated from one another by thin films of protoplasm, which in elongated cylindrical cells are not unfrequently placed across the cell, like transverse septa of cell-membrane, and this position has before now caused them to be mistaken for transverse cell- membranes', The greater part of the 86-94 per cent. of water, which Schlossberger and Dépping féund in fleshy mushrooms, is to be placed to the account of the watery cell-sap. Errera discovered a remarkably large’ amount of glycogen in the cells of many Fungi. This substance permeates the protoplasm, renders it unusually refringent, and may be recognised under the microscope by this quality and by the charac- teristic reddish-brown colour which it assumes in the presence of iodine. It occurs especially in the asci of the Discomycetes and Truffles, but Errera found it also in the vegetative cells of some of these Fungi, of some of the Mucorini, and of certain Hymenomycetes, &c. Nuclei are found in many cells connected with reproductive processes in the Fungi, in asci for example and basidia, and_ their relations to the formation of daughter- cells are in some cases at least clearly understood; but there is some uncertainty with regard to the nuclei in the vegetative cells of the thallus, owing to their minuteness. On the one hand the presence of nuclei in the vegetative cells is probable where they have not been directly observed, because the reproductive cells which have nuclei are formed directly from vegetative cells and are distinguished from them only by their greater size, which may be the ‘only reason why their nuclei are clearly seen, and becatise the nuclein which is characteristic of cell-nuclei has been shown by macrochemical methods to be present in cells, in which the presence of a morpho- logical nucleus is not or has not been certainly ascertained. In conformity with this, Strasburger with the help of colouring reagents detected nuclei in the cells of the thallus and in the spores of the Saprolegnieae, and Schmitz had previously asserted their existence in a number of other Fungi, as for instance in Oidium lactis, in the Peronosporeae, Mucorini, and Saccharomyces; to these may be added Penicil- lium glaucum (Strasburger) and especially the gonidial state of Peziza Fuckeliana (Botrytis cinerea). But on the other hand the objects under consideration, except in the Saprolegnieae, are of such minute size, that the satisfactory discrimination of true nuclei from other small bodies contained in the protoplasm, and like them perhaps rendered more distinct by colouring reagents, is extremely difficult, and can only be obtained after renewed investigations. ‘The accounts in our possession make it distinctly probable that the protoplasm of the elongated vegetative cells of the Fungi which have been examined contains several or even many small nuclei, the division and multiplication of which is not in direct morphological connection with the vegetative cell-division. Only the short vegetative cells of Saccharomyces — according to Schmitz are uninucleate. The reproductive cells to which we have referred above have one or more nuclei according to the species; the connection of the nuclei with the formation of daughter-cells, as far as it is known, will be described below along with the phenomena of reproduction. The protoplasm of the cells of the Fungi contain no chlorophyll or analogous ? See Reisseck in Botan. Zeitg. 1853, p. 337- CHAPTER I.—HISTOLOGICAL CHARACTERISTICS, 7 colouring matter or amylum-grains, nor, as far as is known, any vehicles for colouring matters nor their homologous f/as/éds (A. Meyer’s trophoplasts), It would appear that the formation of fatty matters takes the place very generally of the amylogenesis which holds in plants containing chlorophyll; these matters always form a percentage of the dry substance of vegetating Fungi, and may amount with diminution of the proteid substances to 50 per cent. of the material stored up in the resting-states, to 35 per cent. in the fatty sclerotia of plants like Claviceps, and to go per cent. in the Moulds (? Penicillium) in the resting or involution-stage, that is, after the close of vegetation. During the time of active vegetation the fatty substances are disseminated in the form of minute drops in the protoplasm of the cells of Fungi, as they are in the cells of other plants, and help to make it look granular or turbid; in the resting states (periods of involution), in which reserve-material is stored up, they may collect into large strongly refringent drops which occupy the largest part of the cell-cavity. Examples of the latter case are the sclerotia of Claviceps, the thallus of Sphaeria Stigma, Fr., S. discreta, Schw., S. eutypa, Fr., Vermicularia minor, old moulds, many spores, &c. &c. In many cases the collections of fatty matter are colourless or only faintly coloured, but sometimes they are very highly coloured, if after the analogy of cases which have been carefully and chemically examined we may venture to apply the term fatty substance to bodies, of which we only know with certainty that they agree with fatty aggregates in outward appearance and in the ordinary microchemical reactions. If the bodies in question are really to be regarded as~ chemically definite fats, it still remains to be decided whether the colours belong to the fats themselves, or-are derived from distinct colouring matters which would in that case be attached to the aggregates of fatty matters as their vehicles. With this reservation and pending the requisite strict chemical examination, we may designate as coloured aggregates of fatty substances those microchemically fat-like bodies which produce the characteristic colouring from yellow to brick-red in so many Fungi—Uredineae, Tremellineae, Stereum hirsutum, Sphaerobolus, Pilobolus, many Pezizas as P. aurantia, P. fulgens’, and various other kinds. They are found thinly disseminated in the protoplasm of actively vegetating and growing cells, imparting to it a uniform colouring ; after the death of the cells they often run together into larger drops ; in older cells also they sometimes assume this form spontaneously. In the Uredineae, and according to Coemans in species of Pilobolus also, the red colouring matter shows a characteristic reaction, becoming intensely blue when treated with sulphuric acid, then quickly passing into a dirty green and then gradually losing all colour, a reaction which is seen in the similar red colouring matter of many parts of plants which do not belong to the Fungi, and in the red pigment-spots (eye-spots) of some of the lower forms of animal life. This reaction is not found in the other Fungi mentioned above. These facts sufficiently point. to a different material composition of the bodies in question in different cases: some of them were spectroscopically examined by Sorby. Van Tieghem discovered crysfalloids of albuminoid substance (mucorin) in the gonidiophores and zygosporophores of most of the Mucorini, J. Klein found 1 P. fulgens, Fr., was named P. cyanoderma in the first edition-of this book. 8 DIVISION I.—GENERAL MORPHOLOGY, them previously in Pilobolus. They have the form of octahedra or truncated triangular plates, are extruded from the protoplasm as it is preparing to form spores or sporangia and do not pass into these with the protoplasm; they subsequently. disappear gradually in the decaying sporophore. Section III. The cell-membrane in the Fungi remains thin and delicate to the last in most of the quickly-growing short-lived species; in others, especially in the long-lived solid Mushrooms and Lichens, it is thickened to a variable but often considerable extent, and is in that case stratified like other membranes. Formation of pits has been only rarely observed; fibriform, both spiral and annular, thickenings have been seen only in the capillitium of Batarrea (see Division II). In their consistence and very limited power of swelling, which has not however been accurately determined, the membranes of many Fungi are very similar to the non-gelatinous cellulose-membranes of the higher plants. The elementary composition of the cellulose has also been ascertained by macrochemical analysis after proper purification in a number of cases, in Polyporus igniarius, P. fomentarius, P. officinalis, Agaricus campestris, Daedalea quercina, and Amanita muscaria. But the colourless, non-gelatinous and apparently pure cell-membranes of Fungi of every age are generally distinguished from the typical’ cellulose-membranes of the higher plants by being insoluble in ammoniacal solution of cupric hydrate, and by the absence of their characteristic reactions with iodine; they are not coloured blue by iodine and sulphuric acid or by Schulze’s solution, or only after special and prolonged preparation, in the course of which they often display strong resistance to acids. We may therefore properly distinguish their substance by the special name of /ungus-cellulose. It remains still undecided whether their peculiar qualities are due to the presence of foreign deposits in their substance or to some other causes. ‘Membranes however are not wanting among the Fungi which display the typical blue reactions with iodine ; such are all the membranes in the Saprolegnieae, in Protomyces macrosporus, in the thallus of the Peronosporeae, in the young state of some species of Mucor (M. Mucedo and M. fusiger), and in the cells of the resting perithecium of Penicillium glaucum (Brefeld), Clavaria juncea sometimes, but not always, shows the violet coloration with iodine and sulphuric acid; and this is the case also with the sterile forms known as Anthina pallida, A. purpurea, and A. flammea, which probably belong to Clavaria or its allies. Other Clavarieae show only the Fungus-cellulose. H. Hoffmann’s observations on Amanita phalloides and Agaricus metatus may also be considered in this connection. The non-gelatinous membranes of the Fungi, which are always colourless when young, often become coloured as they grow older, especially in long-lived forms, assuming usually various shades of brown from the lighter to the very darkest brown, more rarely some other colour, as the rosy red of the thallus of the mould, Dactylium macrosporum Fr., the blue of the surface of the thallus of Peziza fulgens, the green of Peziza aeruginosa, and Phycomyces nitens; the varied coloration of the membranes of the spores may also be mentioned here. The colours of the Lichen- fungi will be noticed further on in Division III. Apart from the Lichens, the colouring matter penetrates uniformly through the whole of the membrane or through certain lamellae of it. CHAPTER I,—HISTOLOGICAL CHARACTERISTICS. 9 The coloration of the membrane is accompanied with increased firmness and in most cases with exceptional power of resisting the action of concentrated sulphuric acid, phenomena which taken together recall the similar behaviour of the sclerosed, lignified, and suberised membranes of the higher plants. With the co/oraszon therefore we may also speak of the sclerosts of the membranes. We learn also from other sources that the colouring at least is due to the interposition of substances which can be withdrawn by solvents from the membrane which then remains behind colour- - less, as we can withdraw the colouring deposits from the sclerosed membranes of Pteridophytes, or lignin and suberin from lignified and suberised cell-walls. We cannot at the present day speak of lignification in the strict sense of the word in connection with the membranes of the Fungi, since they do not show Wiesner’s reactions when treated with anilin compounds and with phloroglucin. “Phenomena approaching at least to suberisation in the strict sense of the word appear to occur sometimes, according to C. Richter’s observations on Daedalea quercina. The greater part of the Fungi have not been subjected to any close examination on these points ; the purely empirical expressions, coloration and sclerosis, may therefore serve for the present as general designations of the phenomena. But there is another kind of membrane in the: Fungi which is distinguished from those hitherto described by its gelatinous or even mucilaginous nature. The mem- brane in the dry state is hard and cartilaginous and swells by absorption of water to several times its former volume in the dry state; its consistence therefore in the moistened vegetating state is that of a tough or soft jelly. The outer layers of many filamentous mycelia have this gelatinous constitution, which is very conspicuously seen when the plants are cultivated in a fluid. The hyphae, when examined by transmitted light, appear to have a delicately thin membrane which seems to be surrounded by a hyaline fluid; further examination discloses either a distinct gelatinous sheath round each hypha, or a diffuse gelatinous mass in which the branched hyphae are all imbedded. Zopf observed this in Fumago for example. The phenomena present themselves in a very beautiful form in the Sclerotinieae when cultivated in saccharine solutions. —The membranes of Saccharomyces Cerevisiae must be of this. nature according to the observations of Nageli and Léw. Soft gelatinous membranes also characterise in many cases large masses of tissue of definite shape, which appear at first sight to be slimy mucilaginous masses and may be designated gelatinous tissue (Gallertgewebe) or gelatinous felt (Gallertfilz). Beautiful examples of this formation may be seen among the larger mushrooms in the gelatinous bodies of the Tremellineae, in the gelatinous layers of the peridium of the Gasteromycetes, as Geaster hygrometricus, Melanogaster, Hysterangium, the Phalloideae, Mitremyces, &c. (see Division II), in Bulgaria and Cyttaria, in the greasy slimy superficial layers of the pileus in such Hymenomycetes as Amanita Muscaria, Agaricus Mycena of the section Glutinipedes, Boletus luteus, &c., and in the young mycelial strands of Agaricus melleus (section VII). Membranes of the viscid gelatinous type are found in the elements of most Lichen-fungi, in those of the sclerotia of Sclerotinia and Typhula gyrans (section VIII), of the thallus of Hydnum erinaceus, of the massive sclerotium-like thallus of Polystigma and of the mycelium of Hysterium macrosporum (Hartig). In the three last-named cases and in many Lichen-fungi (see also Division III) the gelatinous membrane-lamellae are coloured 10 DIVISION I.—GENERAL MORPHOLOGY. blue directly by a watery solution of iodine. It is a matter of course that there should be intermediate forms between the highly gelatinous and the non-gelatinous membranes, such as are found for instance among the sclerotia. To the above-mentioned examples drawn from the vegetative parts of the thallus must be added the organs of reproduction, spores and the parts which immediately produce ‘them,—a not less rich and varied con- tingent, of which more will be said in the chapters which deal with these organs. We know very little of the chemical composition of the gelatinous membranes of the Fungi. From the few tolerably precise investigations and from analyses which have been made it seems probable that they are for the most part composed of one or more carbo-hydrates or mixtures of carbo-hydrates nearly allied to cellulose, but with great capacity for swelling. The membranes of the Lichen-fungi (Cetraria, Ramalina, Usnea, and Cladonia) are changed by boiling in water into a homogeneous jelly known as lichenin, the dry substance of which is isomeric with cellulose. According to Nageli and Léw the membranes of yeast-cells (Saccharomyces Cerevisiae), after boiling repeatedly in water, pass partly into a mucilage which they term ‘ yeast-mucilage’ ; the analysis of its dry substance gave a formula very near 3(C6 Hro O5)+H2 O. When the membranes of the Lichen-fungi, especially Cetraria islandica, and of the asci of many of them are coloured blue by the direct action of iodine, the reaction is due to the carbo-hydrate which is mixed with the lichenin (itself not turning blue with iodine) and which can be extracted from it ; its formula is ‘also C6 Hro Os, and it was named by Dragendorff /ichen-starch*. Most of the gelatinous membranes, like the yeast-mucilage, do not take the blue colour; they require further examination. The gelatinous membranes also appear to be in many cases the seats of colouring matters, for instance of the scarlet-red of the surface of the pileus of Amanita muscaria, of the yellow of Boletus luteus, and of others, so that we might conclude that the characteristic colours of the Fungi, with the exception of the reddish-yellow mentioned above, were in almost all cases confined to the membranes. But to microscopic examination in the cases named and in some others the colour appears so pale and so uniformly distributed over the whole cell, that it is difficul&to decide with any certainty whether it belongs to the membranes or to the contents, or whether it is distributed uniformly through them both. A review of the anatomy of the membrane leads naturally to the mention of certain bodies, which are separated out from the cells and are imbedded in or more usually deposited on the membranes, or are interposed in the interstices of the hyphal weft; these are resinous excretions, lichen-acids, and especially calcium- oxalate. The lichen-acids will be noticed again in Division III. Resinous excretions, the histogenetic relationships of which need not be discussed in this place, are known in great abundance as a coating of the hyphae which compose the sporophores of Polyporus officinalis, the mushroom of the Larch, and form sometimes 79 per cent. of the mass of this plant. Bauke? found the hyphae of a Diplodia furnished with a brown ‘resin-like’ covering. Zopf gives a similar account of species of this genus at page 48 of his work on Chaetomium which will be cited ? Berg, Zur Kenntn. d. Cetraria islandica (Diss. Dorpat. 1872).—Niageli u. Schwendener, Das Mikroskop, Aufl. 2, 1877, p. 518. ? Pycniden, p. 35. CHAPTER 1.—HISTOLOGICAL CHARACTERISTICS. Il later. Both the old mycelium and the walls of the perithecia of Eurotium are marked by a similar reddish yellow or golden yellow covering. Calcium oxalate is a substance so generally found in the Fungi that it is atic unnecessary to enumerate instances of its occurrence. I have noticed its absence in the Peronosporeae, in many Hyphomycetes, in species of Bovista and Lycoperdon, and in some Lichens which will be mentioned in Division III. The abundance with which it occurs on or between the cells of the plant varies according to the species, the individual, and the age ; it is often more easy to find in young specimens than in older ones, It not unfrequently appears in the form of regular quadrate octohedra, but more commonly in that of slender needles, or irregularly shaped nodules, or angular granules (Figs. 4 and 5). These occur also on reproductive cells, as in the Mucorineae. When they appear on or in the surface of the plant, they often give it Fic. 4. Hyphae from the surface of a mycelial strand of FIG. 5. Extremity of a hypha of Phallus caninus; a bladder-like cells filled with a crystalline the mycelium of Agaricus camt- sphere of calcium oxalate, 6 small irregular aggregates of the pestris, covered with small acicular same salt on the outer surface of the hyphae. Magn. 390 times. crystals of calcium‘ oxalate. Magn. about 390 times, a chalky white appearance; this we sce in many mycelial strands of Agaricus cam- pestris, in the Phalloideae, in the thallus of Corticium calcareum and Psoroma lentigerum. The occurrence of the calcium oxalate inside the cells, though it has | been observed several times, must be regarded as very exceptional. Small rod-like crystals are occasionally found in the vesicular cells of the stipe and pileus of Russula adusta. On the narrow cylindrical hyphae of the mycelium of Phallus caninus solitary large spherical or flask-shaped vesicular cells are found, which are almost filled by a large glistening sphere of calcium oxalate with a radiating crystalline structure (Fig. 4). Structure of the membrane. I wrote at some length in the first edition of this work on the subject of the structure of the membranes of the vegetative cells of the Fungi, because it was important at that time to prove its conformity with like parts in other plants, in opposition to statements, especially of Schacht, founded on the minuteness of the objects in question, and assuming a much greater general sim- plicity in them. It will be well to repeat here the matter which was then produced, with some abbreviations and additions, notwithstanding the fact that it is now twenty years old, and that modern optical resources have made us acquainted with many further details in the objects observed ; many fresh examples also might be adduced, but they are not required, The young membranes of many woody and leathery Mushrooms, especially the 12 DIVISION I.—GENERAL MORPHOLOGY, Gastromycetes and Mymenomycetes (Polyporus, Thelephora, &c.), is often compara- tively thick, and in an older state is not unfrequently much thickened, even to the obliteration of the lumen. The cells for example of the pileus of Polyporus fomen- tarius, of Crucibulum vulgare! and many other species, have in some parts the appearance of solid cylinders, in others have a distinct cavity. The thickened membranes are either firm and brittle or flexible, or gelatinous and soft. Where the thickening is slight, as on the lateral walls of many Filamentous Fungi (Dematieae, Botrytis cinerea, Peronospora), the membrane is usually homogeneous and not stratified, and even the transverse walls are generally undivisible or with difficulty divisible into two lamellae. But strongly thickened walls often show very distinct stratification without as well as with the aid of reagents which cause swelling of their substance, such as solution of potash or Schulze’s solution or sulphuric acid.- Good examples are the thallus and gonidiophores of Cystopus, and the cells of the firm rind of the mycelial strands of Agaricus melleus; to these may be added the thickened membranes which sometimes occur in Pilobolus in consequence of retarded growth (Coemans). The membranes of many dry resting Fungus-tissues (Polyporus zonatus, P. versicolor, Daedalea, Trametes Pini, Lenzites betulina, the stout hyphae of Thelephora hirsuta, the threads of the capillitium of Bovista plumbea, Geaster, Tulostoma and many others) often show at least two distinct layers, an outer and firmer one which is frequently of a bright colour, and an inner softer and more transparent layer. Further stratification cannot usually be detected in these cases even with the use of artificial means such as boiling in potash, though they may be seen sometimes in an older pileus of Polyporus officinalis. Here may be seen, when the plant is examined in water, an outer thin and apparently firm layer, and an inner thicker and evidently soft layer ; the outer layer is not sensibly altered when warmed in a solution of potash, but the inner swells strongly, so as to protrude like a drop on the surface of fracture beyond the outer layer, and at the same time often separates into numerous delicate lamellae. Very beautiful stratification is also shown in the cells of many Fungi in which the membrane is gelatinous and is capable of swelling strongly in water. In Geaster hygrometricus the inner layer of the outer peridium, which bursts in a stellate manner, consists of straight cell-rows of equal length closely packed together and standing parallel to one another and perpendicularly to the outer layer; they have a thick membrane which is hard and cartilaginous in the dry state, but swells in water to a tough gelatinous consistence and shows in a transverse section three to five lamellae with different refringent power. The outermost lamellae of the cells in adjoining rows are pressed close upon one another, and the bounding lines form a clearly defined network on the transverse section. This structure is often obliterated in old specimens. An exactly similar stratification to that which has been described in Geaster is found in the tissue of Hysterangium clathroides*, which when dry is cartilaginous but swells and becomes gelatinous in water, and also in the inner substance of many sclerotia, as in the Sclerotinieae and in Typhula gyrans. ‘The lower part, the stipe, of the branching body of Calocera viscosa consists of rows of cells all running nearly parallel to the longitudinal axis of the Fungus. Thin transverse sections through the stipe give therefore circular or polygonal sections of the individual cells. The outermost of the three concentric layers of tissue which compose the stipe is in the fresh state of a viscid gelatinous consistence, and is fotmed of slender rows of thick-walled cells which appear‘at first sight to be imbedded in a soft homogeneous jelly. But if thin cross sections of the dried stipe are allowed to swell slowly in water, it becomes apparent in this case also that the jelly is formed of as many gelatinous layers of membrane in close contact with one another at all ? Sachs in Bot. Ztg. 1855. ? See Tulasne, Fungi hypogaei. CHAPTER I,—HISTOLOGICAL CHARACTERISTICS. — 13 points as there are rows of cells. If the sections are kept for a long time in water, the delicate bounding lines of the lamellae disappear and the lamellae themselves coalesce into a homogeneous mass. The above cases establish the occurrence of lamellae of different thickness and capacity for swelling in thickened cell-membranes ; but it also follows from the facts which have been given, that the apparently homogeneous substance between the cells of these Fungi, like the pseudo-intercellular substance in many Fucoideae, Florideae, and others, is not to be regarded as a secreted homogeneous substance distinct from the cell-membrane, but originates in the close contact and partial coalescence of the outer gelatinous thickening-layers of all the hyphae. : The tissues of many Fungi (Melanogaster, Tremella, Exidia, Guepinia, Dacryomyces, Bulgaria, Thelephora mesenterica, Mitremyces, Cyttaria, Panus stypticus), the peridia of the Phalloideae, young Nidularieae, the surface of many Hymenomycetes, as Agaricus Mycena sect. Glutinipedes, Fr., Amanita muscaria, Boletus luteus, and many others, are of gelatinous constitution, and agree in structure with those of Calocera, Hysteran- gium and other forms described above; but the interstitial gelatinous substance appears in most cases to be really a homogeneous mass, and has not yet been separated into portions belonging to the individual cells, This may perhaps yet be done in many of these forms; at the same time it would appear from the published observations on Calocera and from the close affinity and agreement in structure between Calocera, Guepinia, and Tremella, and between Hysterangium and Phallus, &c., that we are justified in considering the homogeneous gelatinous substance of all the Fungi mentioned above as simply a product of the coalescence of soft gelatinous thickening-layers of the cell-membranes. H. Hoffmann seems to take this view’, as he speaks of the gelatinous substance in the outer portions of the pileus of the fleshy Hymenomycetes as a product of the deliquescence of the membrane. The threads of the capillitium in all species, as it would seem, of Lycoperdon (L. pusillum, L. Bovista, L. giganteum; see Division II) are delicately pitted. The thick transverse walls of Dactylium macrosporum, Fr. which are formed of two semi-lenticular lamellae have the large pit in their centre, just in the same way as it occurs in the transverse walls of filiform Florideae like Callithamnion. I have never seen similar pits in other Filamentous Fungi ; their transverse walls are usually delicate, and in some cases, as in Botrytis cinerea, they appear to be thinner in the centre than at the margin. Fungus-cellulose. In my first edition I gave the name of Fungus-cellulose to the substance of the greater part of the non-gelatinous membranes of the Fungi for the reasons given above. C. Richter has recently arrived at the conclusion that there is no special modification of cellulose requiring to be distinguished by such a name, and that the membranes supposed to contain it are composed of ordinary cellulose with foreign, possibly albuminoid admixtures. He shows that the membranes of Fungi like Agaricus campestris, Claviceps, Polyporus spec., Daedalea quercina, and Cladonia, which do not show the characters of ordinary cellulose even when treated in the customary manner with boiling solution of potash, Schulze’s solution, or chromic acid, if subjected to longer maceration in a 7-8 per cent. potash solution do give the ordinary reactions of cellulose, turning blue with iodine and sulphuric acid and with Schulze’s solution, and being soluble in ammoniacal solution of cupric hydrate. The maceration must continue for at least 2-3 weeks, sometimes, as in Daedalea, for as many months. These observations are a welcome confirmation of the near affinity of the substance of the membranes of the Fungi to ordinary cellulose which was indicated by macrochemical analysis; but they merely prove that the membrane of these Fungi is altered by maceration with potash in the way described. Whether * Icon. analyt. fungorum, pp. 12, 25. 14 7 DIVISION I.—GENERAL MORPHOLOGY. this alteration consists in the removal of some substance which was present from the first must remain uncertain; such an explanation has not been proved and others are at least possible. Without going further into the question here, we may merely recall the fact, that ordinary cellulose is coloured blue by iodine when certain reagents have produced certain changes in it; but zinc chloride, for instance, does not in this process remove some admixture which is present in the cellulose and prevents it from turning blue. Old threads of linen and cotton which have been repeatedly washed become blue at once in a dilute solution of iodine ; the changes in their original condition which are thus indicated cannot consist in the simple removal of any substance. From such considerations it appears to me that the cause of the peculiar character of the Fungus-cellulose is not yet ascertained, and the harmless special name for it seems still to be desirable. Coloration. The colouring-matters which are peculiar to the Fungi, i.e. which are produced in their metabolism, are chiefly if not solely the yellow and the reddish yellow which are partly attached to the fatty or fat-like contents of the cells, and partly disseminated through the membranes. It is not therefore too much to say, that all tints peculiar to the Fungi, which do not belong to the first category, proceed from the specific colour of the membranes. An exception to this rule, which may perhaps be regarded as “only apparent, is said to occur in some normally colourless moulds and parasitic forms, which growing in water on a substratum containing soluble red and violet colouring matters take up these unaltered in such a manner that even their cell-contents are corre- spondingly coloured. Fresenius’ makes a similar statement with respect to species of moulds growing among red-coloured Micrococcus prodigiosus, Cohn; I found the same thing in Eurotium and in species of Mucor growing on red fruits and in Phytophthora infestans on red and blue potatoes. But I am now doubtful, firstly whether the colouring of the cell contents is in the protoplasm or in the cell-sap or in both, and secondly whether it is present in the living Fungus, or appears only in those of its cells which have been killed in making the preparation and have then taken up the colouring matter into their protoplasm. One thing remains to be noticed here which has never yet been explained, the colouring of Peziza aeruginosa, P. (Chlorosplenium-aeruginosum of Tulasne)”. This Fungus is found on wood with the green rot so common in forests, the colouring matter of which has been frequently examined since Vauquelin’s time and most re- cently by Prillieux. The green colouring matter of this wood is usually contained in its cell-walls, but sometimes forms according to Prillieux in amorphous masses in the cavities of the wood elements. This is in many cases all that is to be seen; over wide spaces on and in the wood there is no trace of a coloured or uncoloured Fungus to be seen; (Giimbel, Fordos, and myself). Ifa Peziza occurs on and in wood of this kind, almost all parts of it are coloured green, and the colour is in the mem- branes and perhaps also in the interior of the cells of the Fungus, and often in such quantity that the Fungus is more deeply coloured than the wood itself. Single fructifications of the Peziza however rising from the wood are sometimes uncoloured, a pure white, in their upper parts which are farthest from the surface of the wood. These facts taken together led to the view that the green colouring matter is a product of the decomposition of the wood without the co-operation of the Peziza, which takes it up unaltered when it settles in the wood. The fact that Peziza aeruginosa only grows, as far as is known, on this green-rotting wood, and on no other substance, is not in itself a valid objection to this view. But there are on the other hand so many established instances of specific decompositions effected by certain Fungi, that the repeated confirmation of the above-mentioned fact and the absence of other species of Fungus were constantly suggesting the idea that the * Beitr. 80. - * Carpol. III, p. 188. i CHAPTER 1I.—HISTOLOGICAL CHARACTERISTICS, 15 green colour of the decaying wood must be a consequence, and the célouring matter a product of the Peziza which grows in and upon it. The question is still undecided ; but I have myself recently observed the important fact, that green-rotted wood is sometimes found in which microscopic examination can discover no evident colora- tion of the wood elements, but shows the presence inside them of numerous in- tensely green hyphae which most certainly belong to Peziza aeruginosa. All our observations show that the Fungus wherever it occurs always contains the green colouring matter ; it occurs only in green-rotting wood, and the view that the wood owes its colour to the Fungus must be allowed to be probable. The fact that wood is found with this particular form of decay but unquestionably free from the Fungus appears to be quite irreconcilable with this view; but the objection disappears if we suppose with Cornu that the hyphae of the Peziza which vegetate in the wood are short-lived, and convey all their colouring matter to the wood when they die. It ought not to be difficult to settle this question by artificial cultivation. One striking case of coloration may be added here, though strictly speaking it does not belong to our present subject. The tissue of the pileus of certain Boleti, especially Boletus luridus which in the uninjured state is yellow, assumes a blue colour as soon as it comes into contact with the outer air. Schénbein has carefully examined this phenomenon, and finds that it is a substance capable of being extracted from the Fungus by alcohol and probably of a resinous character which turns blue in the air. The blue colour appears in the alcoholic solution under the same conditions as it does in a solution of guaiac-resin, and since it has been proved that the colour is produced in the latter by combination with ozonised oxygen, Schénbein assumes a similar cause of the blue colour in the Fungus. The alcoholic extract from the Boletus does not by itself become blue when exposed to the air; there must therefore be another substance contained in the Fungus, which ozonises the oxygen of the atmosphere, and then effects a combination with the resin, giving off the oxygen to it in the state of ozone. Phenomena of a similar kind observed in other cases confirm this conjecture. Thus both the tincture of guaiac and the alcoholic extract of, Boletus turn blue at once, if they are allowed to fall in drops on the fresh tissue of some of the Agarici which do not themselves turn blue, especially Agaricus sanguineus. The watery juice of Agaricus sanguineus squeezed -out from the’ plant and filtered produces the blue colour at once in both tinctures. From these facts it may be concluded that a number of fleshy Fungi contain a substance soluble in water, which absorbs oxygen and gives it up to other bodies in the state of ozone. The Boleti which turn blue contain this substance with another resinous substance, which like guaiac-resin is turned blue by ozone. Literature of sections II and III :— 1. Cell-structure of the Fungi; structure and chemical composition of the cell- walls. SCHACHT, Die Pflanzenzelle, p. 136 ;—Id. Lehrbuch d. Anat. d. Pfl. COEMANS, Monogr. du genre Pilobolus in Mém. des savants étrang. Acad. Bruxelles, XXX. CASPARY, Monatsber. d. Berliner Acad. Mai, 1855. H. HOFFMANN in Bot. Ztg. 1856, p. 158. H. v. MOHL in Bot. Ztg. 1854, p. 771. DE Bary, Unters. iiber d. Brandpilze ;—Id. Ueber Anthina in Hedwigia, I. 36 ;— Id. in Bot. Ztg. 1854, p. 466. BRACCONOT in Ann. de Chimie, XII. 172. PAYEN, Mémoire sur le développement des végétaux in Mémoires présentés A I’Acad. des sc. de France, IX (1846), p. 21. MULDER, Physiol. Chemie, Braunschw. Pon l pp. 202, 203, where Fromberg’s results are also given. 16 DIVISION I.—GENERAL MORPHOLOGY. SCHLOSSBERGER, Ueber d. Natur d. Hefe (Ann. d. Chem. u. Pharm. 51, p. 206). SCHLOSSBERGER u. DOPPING, Beitr. z. Kenntn. d. Schwimme (Ann. d. Chem, u. Pharm. 52, p. 116. A. KAISER, Chem. Unters. d. Agaricus muscarius L. (Inaugural-Diss., Géttingen, 1862). BURGERSTEIN in Sitzungsber. d. Wiener Acad. 70. C. RICHTER in Sitzgsber. d. Wien. Acad. 83, p. 494. NAGELI u. LOw, Ueber d. chem. Zusammensetzung d. Hefe (Sitzungsber. d. Bayr. Acad. zu Miinchen, Mai 4, 1878). NAGELI u. SCHWENDENER, Das Mikroskop, Aufl. 2, p. 518. FUISTING in Bot. Ztg. 1868, p. 660. See also the literature of the Lichens in Division III. 2. Cell-nucleus, cell-division. SCHIMTZ, F., Ueber d. Zellkerne d. Thallophyten (Sitzgsber. d. Niederrh, Ges. Aug. 4, 1879). ZACHARIAS, Ueber d. Beziehung d. Nucleus, &c. (Bot. Ztg. 1881, p. 169), where other literature is noticed. STRASBURGER, Zellbildung u. Zelltheilung, Aufl. 3, 1880, p. 221, Taf. XIV. 3. Glycogen. ERRERA, L., L’épiplasme des Ascomycétes et le glycogéne des végétaux (Thése, Bruxelles, 1882) ;—Id. Sur le glycogéne des Mucorinées (Bull. de PAcad. de Bruxelles, Noy. 1882). 4. Cell-contents, fat, crystalloids. NAGELI, Ueber d. Fettbildung bei d. niederen Pilzen (Sitzgsber. d. Bayr. Acad. Miinchen, 1879, p. 287). ROSTAFINSKI in Bot. Ztg. 1881, p. 461. SORBY, On comparative vegetable Chromatology (Proc. Roy. Soc. London, XXI, p- 442). See also Just’s Jahresber. 1873. VaN TIEGHEM, Nouvelles recherches sur les Mucorinées (Ann. d. sc. nat., Sér. 6, I, p- 24). See also the literature at the end of sect. XLIV. 5. Resinous secretions. HARZ in Bull. Soc. Imp. de Moscou, 1868, 6. Green rot in wood. VAUQUELIN in Ann. du Mus, dhist. nat. VII, p. 167 (1866). GUMBEL in Flora, 1858, p. 113.” BLEY in Arch. d. Pharmac. 1858. FORDOs in Comptes rend. Acad. d. sc. Paris, 87, p. 50 (1863). ROMMIER in Comptes rend. Acad. d. sc. Paris, 66, p. 108 (1868). PRILLIEUX in Bull. Soc. Bot. de France, 1877, p. 167. CORNU in Bull. Soc. Bot. de France, 1877, p. 174. 7. Boleti which turn blue. SCHONBEIN in Verhandl. d. naturf. Ges. Basel, 3 (1856), p. 339 ;—Id. in Abhandl. d. K. Bayer. Acad. VII (1855), and in Bot. Ztg-: 1856, p. 819 ;—Id. in Bull. de lAcad, de Belgique, Sér. 2, VIII, pp. 365, 372, and_in Comptes rend. Jul. 16, 1860. CHAPTER I1I.—DIFFERENTIATION OF THE THALLUS. 17 It does not fall within the scope of this work to go into the details of chemical analysis ; the reader is referred for these to— Husemann und Hircer, Die Pflanzenreiche, Aufl. 2. See also the first edition of A. and Th. Husemann. Friicxicer, Pharmacognosie d. Pflanzenreichs, Aufl. 2, Berlin, 1883. The work contains exact accounts of Claviceps, Polyporus officinalis, Cetraria, &c. G. Dracenporrr, Die qualitative u. quantitative Analyse von Pflanzen u. Pflanzentheilen, Géttingen, 1882. J. Kéyic, Chemische Zusammensetzung d. menschlichen Nahrungs- u. Genuss- mittel, Berlin, 1878 (Edible mushrooms). CHAPTER II. DIFFERENTIATION OF THE THALLUS. 1, GENERAL SURVEY. Section IV. The thallus ofthe greater part of the Fungi which are composed of hyphae is differentiated into two chief parts, a vegetative part known by the name of mycelium since the time of Trattinick’, and the sporophore* (Fruchttrager, receptaculum of Leveillé, encarpium of Trattinick), which bears and produces the organs of repro- duction and springs often in great numbers from the mycelium. It need scarcely be said that there are many gradations in the sharpness of this differentiation. The views and the terminology drawn from the species in which the differentiation is sharply defined have often been transferred to those in which it is less distinct. In simple filamentous forms, as Protomyces for instance and Entyloma, in which the repro- ductive cells are formed directly as segments of hyphae which are not further differentiated, we speak of these cells being formed directly on the mycelium. In many cases this distinction between mycelium and sporophore may be said to be. only arbitrary. - Owing to the peculiar mode of life of the Lichen-fungi, the differentiation in many of them is to some extent different from that of the rest of the Fungi, and the traditional terminology therefore, which will be considered in Division III, is also different. ? The mycelium is that part of the thallus which spreads in or on the substratum, derives nourishment from it and attaches the Fungus to it. In accordance with these functions it resembles the root-bearing rhizomes of the higher plants, and still more the rhizoids of Mosses in various points of form and growth. The sporophores may be compared to the flowering or fruit-bearing shoots of higher plants in respect of their function to which their form corresponds, and which consists essentially in the formation of organs of reproduction. 1 Fungi austriaci, 1805. * See note at beginning of section X regarding the use of the term sporophore. [4] > Cc 18 DIVISION I.—GENERAL MORPHOLOGY, 2. THE MYCELIUM. Section V. The mycelia in their original form are always free hyphae; they either retain this character during their whole life, or the hyphae as they grow become at most loosely interwoven with one another without forming bodies with a definite shape and outline, filamentous or floccose mycelia; or the hyphae form by their union elongated branching s/rands (fibrous or fibrillose mycelia), or membranous expansions, or tuber-like bodies, sclerotia. The filamentous mycelia are much the most common, and in the majority of Fungi they are the only known form. Their character has been already described in speaking in the first chapter of the hyphae of the Fungi generally. The branching of the mycelial filaments in-all cases that have been observed with certainty is mono- podial. The phenomena of coalescence of hyphal cells that were originally free, and of clamp-connections which were described above, appear as a rule in their most striking form in filamentous mycelia. Differences in the structure of mycelial filaments must necessarily depend chiefly on the presence or absence of a regular system of transverse walls, and this, as has been already intimated, varies in the different groups. (See also Chapter V.) Every species in each of the two chief categories thus obtained exhibits as a rule its own peculiar phenomena of growth and differentiation, provided the normal conditions of growth remain unchanged, and by these phenomena the several species and groups of species can be distinguished from one another. These differences relate to the average size and special form of the cells, the divergence of the branches, the phenomena of coalescence and the like. Owing to the diminutive size of the objects, they are usually very inconspicuous even under the most favourable conditions of growth, _and to ascertain them with certainty requires careful observation. They are liable also to so many changes from external causes that the determination of a mycelium, which under favourable conditions of development has well-marked characters, without its sporophore may be attended with considerable difficulty in practice, if it has to be observed under less favourable circumstances. Much advance has been made in this point of late years through the careful examination of individual species, so that we may expect that the morphological characters of the mycelia of many species and groups of species will in time be clearly determined. Some filamentous mycelia, belonging to species from very distinct groups, are distinguished by having special organs of attachment and suction, known as haustoria; these are peculiar branches which attach the mycelium firmly to the substratum, and in most cases also evidently serve to take up nutriment from it. Such organs are found in many, but by no means in all, parasitic species living on plants and. belonging to very different groups, as the Peronosporeae, Piptocephalis, the Uredineae, and Erysipheae, The mycelial filaments of these Fungi spread themselves on or among the cells of the host ; the haustoria are formed on them as special lateral branches which force their way into the interior of the cells; they vary in form according to the species and are more or less, often extremely, unlike the extracellular hyphae. Organs of attach- ment, which at least very nearly resemble the haustoria of these parasites, are found in a few other non-parasitic mycelia; they will be noticed again subsequently. CHAP, II.—DIFFERENTIATION OF THE THALLUS,—-FILAMENTOUS MYCELIA. 19 Careful investigations into the formation of the mycelia of distinct species of non- parasitic Fungi are to be found especially in Brefeld’s Untersuchungen iiber Schim- melpilze. The formation of clamp-connections described above may be taken as an example of a peculiarity which is characteristic of the larger groups. It occurs, as far as we at present know, almost exclusively in the Basidiomycetes and chiefly in the Agaricineae ; it is found in the Tuberaceae, but apparently in no other Ascomycetes. Its occurrence in Peziza Sclerotiorum, as stated in my first edition, seems not to be confirmed in more FIG. 6. a and b Podosphaera Castagnet, Lévy. a epidermal cells of Melampyrum sylvaticum ; a branched mycelial hypha is creeping over the surface and has sent a haustorium into one of the cells (surface view). 4 vertical section through epidermal cells with mycelial hypha and a haustorium which has penetrated into a cell. ca spore (gonidium) of Erysiphe Umbelliferarum putting forth germ-tubes on the epidermis of Anthriscus sylvestris. The smaller gerin-tube on the right is sending a haustorium from the lobed attachment-disk into an epidermal cell. @ and 4 magn. 600, ¢ 375 times. recent times. It is at present uncertain whether it is a feature of all the Basidiomycetes or only of all the Agaricineae, and the more so as according to Brefeld it is frequent in one species of the genus Coprinus, but comparatively rare in all the rest. A greater number of distinctly marked characters have been observed in the mycelia of parasitic Fungi, especially the Erysipheae, Peronosporeae, Uredineae, and Ustilagineae than in other forms, and they have been observed for a longer time. Such characters occur chiefly in the formation of the haustoria of many species and groups of species in those divisions ; the following are examples of them. The mycelial filaments of the Erysipheae (Figs. 6, 7) are furnished with transverse walls, and their numerous but distant branches spread themselves over the epidermis of phanerogamous plants, being generally closely applied to it, but at the same time easily |... 1. Bedeipie (onaeeay Thebes” Wy. separable from it. At certain circumscribed spots, how- celial hypha with lobed attachment-disk on ever, they are firmly attached to the substratum, and 70 u3°S, xiv Mage so tne in these spots they are provided with a haustorium which, springing as a branch from a cell of the mycelium in the form of a very delicate tube, pierces the outer wall of the nearest cell of the epidermis and enters its cavity; there it enlarges into an ellipsoid or somewhat elongated persisting vesicle filled with protoplasm, which in Erysiphe graminis is branched in a peculiar manner. The C 2 20 DIVISION I,—GENERAL MORPHOLOGY. mycelial filament according to the species-is either not altered at all at the point of origin of a haustorium, or is at most only slightly enlarged there ; or it has a flat nearly semicircular protuberance the height of which is at most equal to its own diameter ; or it has a protuberance in the form of a bluntly lobed disk scarcely exceeding the breadth of the filament, which is pressed closely down on the epidermis, and appears on both sides or only on one side beyond the flank of the filament. These lobed attachment- disks were first discovered by Zanardini in Erysiphe Tuckeri. : The thick mycelial tubes of the Peronosporeae, which are usually without transverse walls and spread among the cells inside living plants, often clinging close to the outer surface of their walls, send haustoria into. the cells, which have very different forms in the different species. In Cystopus (Fig. 8 4), Peronospora nivea, P. pygmaea, P. densa and others, they are like those of the Erysipheae but much smaller, and they usually or perhaps in all cases only make a deep indentation in the walls of the cells ; in P. parasitica they are lobately branched tubes, and their vesicular club-shaped branches often quite fill the cells of the host; in most of the pleuroblastic Perono- sporeae (Fig. 8 &) they are slender filiform lateral branches of the in- tercellular filaments with many curved and winding ramifications in the interior of the cells. In Phy- tophthora infestans, which inhabits the potato, branches of the myce- lium which in this case scarcely FIG. 8. Mycelial tubes creeping about in the intercellular spaceswith deserve a separate name force their their haustoria penetrating into the cells e—z; 4 of Cystopus candidus, s . : from the pith of Lepidium sativum, B of Peronospora calotheca from the way at various spots, especially in pith of Asperula odorata, Magn. 390 times, _ the sprouting tubers, into the cells of the host. The intercellular mycelium of the Uredineae has a variety of haustoria formed like those of the Peronosporeae, especially the pleuroblastic species, and with them should be _mentioned also the winding intracellular mycelial branches of the Ustilagineae. _ The haustoria of Piptocephalis, Syncephalis, and Mortierella are very different from those which we have hitherto been considering. Piptocephalis Freseniana is parasitic on the larger Mucorini, and its mycelium, like that of its hosts, con- sists of tubes without transverse walls. If a growing filament of the mycelium of the parasite comes in contact with a mucor-tube, either with its apex or with its lateral wall, it spreads out slightly at the point of contact and thus attaches itself firmly as with a cupping-glass to the Mucor. A tuft of filiform radiating branching processes of such extreme delicacy ‘that nothing is known of their minute structure now shoot forth from the middle of the surface of attachment into the cell of the host. The length of these suction-filaments is about equal to the diameter of the mucor-tube | (see section XLIII). Van Tieghem and Le Monnier describe similar arrangements in Mortierella and Syncephalis, only in these genera the tubes which enter the cells of the host are not so different from those of the rest of the mycelium. An allied case, though with important points of difference, is that of the clusters of haustoria in Chaetocladium Jonesii, a form which is usually parasitic on species of Mucor like the genera just described, and resembles them in structure. The tubes of this Fungus, both of its mycelium which spreads in the substratum and of the part of its thallus which rises above it, become firmly attached at the point of contact to the == 3 / Ry 7° PD Sap! Beye in te Arwiny oy 5 i na yer oead ek wy ber - CHAPTER II.— DIFFERENTIATION OF THE THALLUS.—MYCELIAL LAYERS. 21 mucor-tubes which they encounter, and enter into open communication with them at this point by the dissolution of the cell-membranes and complete coalescence of the protoplasm of both plants. At these points of union they now put out small vesicular projections, which in strong specimens appear in numbers close together and form clusters which may reach the size of a pin’s head. It is obvious that these vesicles do not, like the haustoria in the previous cases, serve as organs of attachment and nutrition, for organs of the kind are rendered unnecessary by the union of the parasite and the host. They are-evidently storehouses of food-material, and the fertile branches of the thallus spring chiefly from them. But in relation to the morphological points at present under consideration they are in their nature essentially branches of the mycelium, which however stand in the closest and most exclusive relation to the physiological function above mentioned. Organs of attachment of an unusual kind resembling haustoria are peculiar to the species of Sclerotinia which have been examined, S. tuberosa, S. Sclerotiorum, S. ciborioides, S. Fuckeliana, and also to the gonidial state of this species known as Botrytis cinerea. Under conditions to be described in the sequel the mycelium of these plants, often when still quite young, forms short branches on which arise tufts of secondary branches, which becoming closely clustered together are divided by numerous transverse walls into short segments with membranes that become dark brown with time. The clusters may be of the size of a pin’s head, and have then ‘been mistaken for sclerotia, with which however they have no connection. They are formed when the mycelium under conditions of plenteous nourishment is growing on a solid substratum, such as a plate of glass, which it cannot penetrate, and they apply themselves closely to the substratum. On substances into which the plant penetrates, such as the parts of plants which are suited to it, the tufts are not formed at all or are only feebly developed, in which case their branches soon pass into the substance of the host and grow there into slender branches of the mycelium. Brefeld gives figures of these formations in his Schimmelpilze’. Section VI. The mycelial hyphae of many Fungi, when the conditions are favourable, become interwoven with one another and form membranous layers which may be of considerable extent and thickness. This is the case with such Hyphomycetes as Aspergillus niger, A. clavatus, and Penicillium glaucum, which in their simpler condition have a filamentous and floccose mycelium, if they grow on the surface of a moist nutritive substratum. They some- times form large expansions on the surface of fluids, and may be lifted off them like a cloth, The free surface of the mycelium is in these cases usually clothed with the filiform sporophores. A second series* of examples is supplied by many, perhaps by the larger part, of ‘the solid and especially of the woody and wood-inhabiting Hymenomycetes, the mycelia of which form very thick membranes or crusts, sometimes of considerable breadth and some millimetres in thickness, on the free surface of the substratum or in clefts inside carious stems of trees. Sporophores spring on the one side directly from the membranes, and on the other single filaments or bundles of filaments branch off from them and penetrate into the substratum. Other instances occur here and there in other groups, and are mentioned in special publications*. Apart from the exceptional case of Agaricus melleus which will be described below, the only general remark of importance upon the structure of these mycelial ' Schimmelpilze, IV, t. IX. ? See the literature cited at the end of the chapter. 22 DIVISION I.—GENERAL MORPHOLOGY. membranes, which our present knowledge enables us to add to what has been already | said, is that they only occur in Fungi with septate hyphae; the structure of the mycelium varies of course in particular points in each species. Special generic and specific names have in former times been repeatedly given to mycelial membranes which are only known in the sterile state. Persoon’s genus Mycoderma* may be composed to a great extent of forms of this kind which belong to the Hyphomycetes or to the Ascomycetes. Racodium cellare of Persoon? which forms the well-known olive-brown coating on old casks in cellars is, as far as we know, a mycélium formed of loosely interwoven filaments, the origin and reproductive organs of which are still quite unknown. The mycelial membranes named by Tode and Persoon Athelia and Xylostroma are of a firmer kind. The Athelieae are the sterile states of the Thelephoreae (Thelephora, Hypochnus), in part perhaps their undeveloped sporophores ; the Xylo- stromeae, which occur as broad flat formations of a woody or leathery texture in the decaying stems of trees, are the like states of firm wood-destroying Hymenomycetes, such as Polyporus abietinus, Thelephora hirsuta, Th. crocea, Schrad., Th. setigera, Fr., Th. suaveolens, Trametes Pini, Daedalea quercina, and other species of these and allied genera. Section VII. The hyphae of the mycelia of many Fungi unite together into strands, which in their form, branching, and mode of spreading in the substratum look to the unassisted eye more or less like the roots of higher plants. Even some species of Hyphomycetes, those for instance known as Acrostalagmus, show a tendency to this kind of formation. But it is most frequent among the Fungi which have compound sporophores, such as the Phalloideae, many Lycoperdaceae, the Hymenogastreae, Nidularieae, and Sphaerobolus, in many of the Agaricineae, as A. campestris, A. praecox, A. dryophilus, A. aeruginosus, A. metatus, A. andro- saceus, A. Rotula, A. platyphyllus and A. melleus, and amongst Ascomycetes, such as Elaphomyces, some species of Genea, Peziza Rapulum, Bull., and P. fulgens; the endophytic mycelium of Polystigma stellare, Lk., may be added to the list. It is evident from these examples that the formation of strands is not necessarily found in all the species that belong to the cycles of affinity indicated by the above names; on the contrary it may be wanting in one of two nearly allied species and be found in the other. The strands, as has been said, spread themselves out in and on the substratum, growing at the apex and putting out similar branches, the arrangement of which scarcely follows any exact rule even in the same species. In each-case the strands may either be in part free and tapering, or they may in part unite to form a coarser or finer net-work, or they may in part lose themselves in a loose filamentous web, or a single strand or several combined may expand into membranes, which spread over the substratum or spin themselves round bodies contained in it. Fresh strands may then take their rise from these expansions. This variation of form is essentially dependent on the character of the environment and its influence on the nutrition of the Fungus, as is well shown in the case of Agaricus melleus to be hereafter described. - In most cases which have been examined the strands are composed of uniform ? Mycol. Europ..p. 96. * Syn. Fungor. 701. CHAPTER II.-—-DIFFERENTIATION OF THE THALLUS.—-MYCELIAL STRANDS, 23 hyphae with transverse septation, which vary according to the species. They generally run parallel to the longitudinal axis of the strands and are straight or undulating, and are either grown together by their lateral walls, as in Polystigma stellare, Agaricus Rotula and A. metatus, &c., or they are loosely woven together, as in Elaphomyces, the Nidularieae, Scleroderma, and the Hymenogastreae. The structure of such Phalloideae as have been examined, of the Lycoperdaceae and of some Agarici, is somewhat more complicated. The strands of Phallus impudicus creep in the ground and may be several feet in length and 2 mm. in thickness. A transverse section through the stronger branches shows a thin, firm, white, outer layer or rind enclosing a thick cylinder of a brownish colour and gelatinous appearance (the medulla). The central and larger portion of the medullary substance consists of a felt of tough gelatinous character, in which the hyphae run longitudinally and are slightly sinuous and of unequal thickness. The outer portion of the medullary substance is exclusively formed of thicker hyphae. The rind is composed of a few layers of broad thin-walled hyphae wound firmly round the medullary cylinder in narrow spiral coils. It is easy to see that these hyphae spring as branches from the peripheral elements of the medullary tissue, then curve outwards and join the tissue of the rind. They form on their surface short distant branchlets which make the strands appear as if clothed with short hairs. The entire surface of the strands is covered with calcium-oxalate. The strands of Agaricus platyphyllus’ are very like the above in thickness, appearance, and structure, only the hyphae all run in the longitudinal direction and their walls are on the whole of firmer texture. The strands of Phallus caninus resemble likewise those of Ph. impudicus, but are smaller in every respect. Here too all the hyphae run parallel to one another in the stouter parts which may be t mm. in thickness, and the white rind is distinguished from the yellowish gelatinous’ medullary substance which contains no air by more loosely interwoven hyphae, by air-filled interstices, and by the copious deposit of calcium-oxalate on the hyphae and in the vesicular cells described on page 11. Clathrus shows similar characters as far as my observation has gone. The rind and the medulla are often less distinctly separated from one another in the more slender branches of higher orders, but the former is always distinguished by its covering of calcium-oxalate. ‘The strands of the Agarici (Agaricus campestris, A. aeruginosus, and A. praecox) and those of the Lycoperdaceae have the appearance of the slenderer branches of Phallus caninus and the same structure in all important points. The presence of the calcium-oxalate varies according to the genera and species, as was stated on page Ir. The formation of strands reaches its highest development, as far as is at present known, in the mycelium of Agaricus melleus. An excellent description ofthe structure and growth of this plant by Jos. Schmitz was published, with some additions by | myself, in the first edition of this work ; its life-history was elucidated by R. Hartig, and our knowledge of it was subsequently completed by Brefeld’s cultures. ‘There is the more reason for giving an account of the results of these investigations in this place because Agaricus melleus is the only one of the forms which we are at present considering in which the course of development has been followed from beginning to 1 See Fries, Icones sel. Hymenomycetum, I, t. 61. “at DIVISION I,—GENERAL MORPHOLOGY, end. Agaricus melleus is chiefly a parasite on living European Abietineae (see Division III). It makes its way into the roots or the base of the stem beneath the ground, and the mycelium spreads in the cambium zone and in the young bast, forming FIG. 9. Agaricus melleus. Me- dian longitudinal section through the growing apex of a subterra- nean mycelial strand, seen by trans- mitted light. Magn. 40 times. tt) ie WN Ns : IgE aciety i EROS Pn CREO HHT LE et Sta iy HA i FIG. 10. Agaricus melleus. Thin median longitudinal section through the extremity of the growing apex of a subterranean mycelial strand. Magn. 250 times, but the drawing completed under higher magnifying power. Yi jee Mi I] | compressed or membrane-like expanded networks of strands at the cost of the sap- % containing layers of tissue, and also sends out a large number of single hyphae from these strands into the rind and wood, and especially into the medullary rays, where they spread widely. From these zfra- matrical, especially subcortical, parts other strands may proceed which develope as extramatrical strands usually in the soil, and are therefore sub/erranean, and branch and spread the Fungus over wide distances from one tree to another. These strands become more than 3 mm. thick and are oy th Meanie, eo2 oH ses ~@egsrerg Yer TK) acV {) 6a Ra FIG. 11. Agaricus melleus, Transverse section through a young branch of a subterranean mycelial strand in about thes lower half of Fig. 9. @ the axile large-celled tissue passing towards the outside into the later-formed rind. The outer limit of the rind is at 4; outside 4 is the covering of gelatinous felt with numerous spreading hair-like branches %. Magn. 190 times, round on the transverse section; they can - also develope into enormous masses in moist rotting timber. The cylindrical subterranean strands consist when fully formed of a dark-brown, brittle, usually smooth peripheral tissue or rind enclosing a white finely-felted me- dulla. The rind, which in stout specimens has the thickness of paper, is formed in its outer portion of about twelve or more layers of cell-rows (hyphae) running down the Jength of the strand, and connected with one another laterally without interspaces, 4 CHAPTER II,—-DIFFERENTIATION OF THE THALLUS,—-MYCELIAL STRANDS. 25 The cells of the hyphae are 2-4 times longer than broad, and have a firm brown membrane and a polygonal transverse section in conformity with the absence of intercellular spaces; the cells of the outer layers are narrower than those of the inner and have much thicker walls. The stratification of their membranes becomes more conspicuous when they are treated with potash. © The medulla consists chiefly of slender tough longitudinal hyphae about 1.5 mm. in thickness, which form acute angles with one another as they interweave, and have air in their interstices. Their membranes are comparatively firm; septation and branching are rarely seen in full-grown specimens. The slender medullary hyphae are in connection with the innermost layers of the rind; longitudinal sections show them arising as numerous branches from the cells of these layers, and making their way between them or running directly from them in oblique or transverse course to the medullary tissue. The longitudinal arrangement of the layers bordering on the medulla is thus rendered irregular to a degree which varies in each specimen and is sometimes considerable. I have observed the development of the subterranean strands on adventitious branches, which it is not difficult to obtain from old specimens if cultivated in a damp chamber. The apex ofsuch a branch, as it rapidly elongates (Figs. 9 and ro), is conical in form and colourless for a distance of some millimetres. It consists of a weft of delicate hyphae rich in protoplasm, the terminal branches of which form at the apex a loosely tangled tuft rendered slimy by the gelatinous swelling of the membranes. The apical tissue is continued downwards in the periphery of the branch into the gelatinous felt which covers it and which will be described presently, and in the middle into a short-celled irregular tissue of interwoven hyphae without interspaces, which forms the real conical growing point of the body of the strand. Active meristematic cell-multiplication, which cannot be followed in detail on account of the close interweaving of the hyphae, takes place in the uppermost region ; close beneath this, where the strand begins to grow broader, there is partly elongation and extension of the elements of the tissue, partly formation of new elements. The former affects first and chiefly the axile portion of the strand, which occupies a third part of the total thickness; its cells subsequently undergo a few divisions close beneath the growing point and expand rapidly to a breadth of about 12-20 » and 2-8 times that length ; they continue thin-walled, are filled chiefly with hyaline cell-sap and are arranged in straight longitudinal rows. ‘They diminish gradually in breadth as they approach the peripheral tissue (compare Figs. ro and 11). An evident elongation of the cells takes place in the peripheral tissue, which serves to show more clearly their arrangement in longitudinal rows, but the increase in breadth is only small. As the circumference of the strand increases with every successive transverse section from the apex of the cone to the fully formed cylinder, and the hyphae are in close contact with one another without interstices, there must necessarily be an interpolation of new hyphal branches between those already formed. The development of the definitive structure of the strand begins with the passage into the ultimate cylindrical form. The increase in the breadth of the large axile cells ceases near the apex, where the peripheral layers of the circumference increase con- siderably ; the consequence is that the axile cells are torn from one another especially laterally, and intercellular spaces are formed between them, which serve from the first S 26 DIVISION I.—GENERAL MORPHOLOGY. to conduct air (Fig. 10). The spaces widen most in the centre of the axile strand ; in the simplest case a single large axile cavity is formed, and narrow air-spaces join on to it on the side of the periphery; in other cases single rows of cells remain in the centre of the cavity separated for the most part from the adjacent tissue and each quickly drying up; here too therefore there is really an air-filled axile cavity; i diameter varies much, but it is always at least half as large as that of the strand, ee in strong specimens may reach a much larger relative size. The wall which encloses the cavity consists in its immediate vicinity of the original large axile cells; these form about six irregular layers round the cavity, the cells of the outer layers becoming gradually narrower, as was stated above, and it is these layers which give rise to the medulla of the fully formed strand in the way which will be described presently. Outside of the zone which produces the medulla are the numerous layers of the close compact tissue, which ultimately forms the rind of the strand. ‘This tissue does not however extend to the surface ; this is occupied by a supplementary stratum of about six layers of hyphae with narrow lumina and thick gelatinous walls, which have coalesced into homogeneous mucilage, the gelatinous felt mentioned above. The hyphae of this tissue run for the most part longitudinally, and join with the hyphae of the apical tuft. They also give off spreading branches from the surface. From these must be distinguished other spreading branches, also provided with gelatinous walls, which spring from the hyphae of the rind beneath the gelatinous felt, and pass transversely through it towards the outside. Their number and distinction vary in individual specimens, and according to Hartig they are of special importance when the Fungus finds opportunity for adopting a parasitic life. A sharply defined boundary line between the innermost elements of the gelatinous felted layer and the outermost of the later rind cannot be drawn in the earlier stages of development. The assumption by the tissue of its ultimate form begins with the thickening and turning brown of the walls of the hyphae. It advances on the transverse section from without inwards, and its first beginnings may be followed upwards to the base of the young apical cone. As the coloration advances the gelatinous felt which covers the rind dries up and usually no trace of it remains in older strands. At the same time the formation of the ultimate medullary hyphae begins inside; these arise, as is shown in Fig. 12, as slender lateral branches from the cells of the zone which produces the medulla, and from the innermost layers of the rind which are not sharply distinguished from it; these branches elongate and ramify and enter the axile cavity, and becoming woven together there fill it up in the manner which has been already described. As the zone which produces the medulla always consists of several layers of cells, the hyphae which proceed from its outer layers into the cavity must force their way between the inner layers, which may become much displaced and squeezed together, and this gives rise to the irregularly constructed boundary zone between the medulla and the rind which was mentioned above. A subterranean strand may form branches of the same kind in varying number and with no regular arrangement. At the point where a branch subsequently appears, a new formation in the form of a thick cushion of pseudo-parenchyma is developed within the inner layers of the rind by shoots from its cells, and the growing point of the strand emerges in a few days from CHAPTER II.—DIFFERENTIATION OF THE THALLUS-—MYCELIAL STRANDS, 27 the cushion, and breaking through the rind of the parent-strand grows in the manner which has already been described. Its final medullary hyphae become continuous with those of the medulla of the parent-strand. Schmitz first observed that, at least when old strands are cultivated in a damp chamber, the place of every future branch is indicated some days before its emergence by the appearance of a floccose tuft of hyphae 4—1 mm. in size, arising partly beneath, partly also according to Hartig out of the surface of the parent-strand, which decays and disappears as the branch is formed. The stronger subcortical strands and the membrane-like expansions in the living tree are said by Hartig to be similar to the subterranean ones just described in structure and development, except in respect of certain differences arising from difference of form, the somewhat smaller masses of tissue, and the fainter tinge of brown on the outer Jayers of the rind or the entire absence of that colour. Very delicate myce- lial membranes and slender tufts of ramifying branches, which frequently arise on the edge of the larger mycelial body, have a more simple structure and consist only of hyphae of the rind. There is ene important pecu- liarity in all these strands and expansions, that the numerous hyphae which stand out like hairs from the surface force their way into the tissue of the rind and wood, and spread and ramify there, and are organs by which the Fungus takes up its food. They often form bladder-like swellings in the tracheides of the pine-wood which they decompose, reminding one of the inner layers of the rind of the strand, and their number in the tracheides may be so large as to fill them with a tissue of bladder-like ~ gu ia ee rene eer re Brefeld has completed our knowledge of Se rae ee tee ae es the life-history of the mycelium of Agaricus melleus by growing it from spores in an artificial nutrient solution (decoction of plums). A delicate branched radiating primary mycelial hypha was developed in about eight days from the germ-tube which issued from the spore cultivated on a microscopic slide. Thick tuft-like branchlets from single branches of the hyphae or from several adjacent ones then. appeared in the centre of the circular expansion which was some millimetres in size; these tufts raised themselves erect and became united together into clews as large, according to the figures, as a good-sized pin’s head, after the manner of the sclerotia to be described below in 1 R. Hartig, Die Zersetzungserscheinungen d, Holzes, p. 59. 28 DIVISION I.—GENERAL MORPH OLOGY, section VIII. The clews assumed a pseudo-parenchymatous structure owing to the swelling of the cells of the hyphae, and the greater part of their surface acquired a brown colour. Then one or several growing points appeared on most of the clews, always at isolated uncoloured spots in the part which did not project above the.nutrient solution, and from these points mycelial strands were developed of the subterranean form just described. ‘The primary mycelial hypha ceases to grow when the formation of strands commences; the strands also cease to grow as soon as the supply of nutri- ment is exhausted. When cultivated on bread or with a larger supply of the nutrient solution they developed vigorously and branched copiously, and showed all the important points of the subcortical form described above. They remained uncoloured beneath the substratum, and cessation of growth in length was followed by specially copious development of gelatinous hyphae spreading from the surface, and forming on the top of the fluid thick membrane-like patches of wefted covering with a vesicular pseudo-parenchymatous structure, and with the cell-walls coloured brown where they were in contact with the air. After a winter rest of several months’ duration a large number of strands of the subterranean form were again produced from the cultivated specimens, being fed by them, and they were seen to make their way into the roots of living pines, where their further subcortical development was also observed. The development of the sporophores, which will be described in Division II, begins according to Hartig on strands of both kinds in the same manner as the formation already described of similar branches on the strands. Further details and variations, the great abundance of which is not to be wondered at, considering the great variety of form and adaptation displayed by the strands of Agaricus melleus, are to be found in the works of Hartig and Brefeld which are cited further on. I have endeavoured to correct my own former statements, and some also of those writers themselves, from these researches and some more recent ones of my own. Some statements have not been satisfactorily explained even by these investigations ; among them a former remark of mine in the first edition of this book, that old and strong specimens of the subterranean form ‘have often an uneven and wrinkled rind, in which through subsequent luxuriance of growth the number of the cell-layers is considerably increased and their arrangement is disturbed. I often but not always found inside these specimens a brown zone concentric with the rind from which it is divided by a narrow layer of ordinary medullary tissue, and enclosing a strand of the latter tissue. This zone consists of hyphae with brown membranes very tightly interwoven with one another, but in other respects resembling the ordinary elements of the medulla, into which it passes without a break. Eschweiler’s account of the structure of the Rhizomorphae is founded on the examination of such specimens.’ Future investigations will perhaps clear up these less important points. Greater interest attaches to the question, whether the first development of the mycelium observed by Brefeld, and especially the primary formation of the subterranean strand, is an invariable occurrence in Agaricus melleus, or whether perhaps the subcortical formations do not proceed directly from the mycelial hyphae, when the spores germinate on a substratum which renders parasitic growth possible, that is upon the living root of a conifer. The history of our knowledge of the mycelium of Agaricus melleus is somewhat remarkable. Before R. Hartig discovered that the strands belonged to this Hyme- nomycete, they were supposed to represent a distinct species of Fungus which was named by Roth Rhizomorpha fragilis, or the two forms, the subterranean and the subcortical, were made two distinct species, Rhizomorpha subterranea and Rh. CHAPTER II,——-DIFFERENTIATION OF THE THALLUS.—MYCELIAL STRANDS. 29 subcorticalis, Persoon. The attempts to find the fructification of these Fungi led to the most divergent views; but there is no need happily to repeat here and criticise the complete enumeration and examination of them which was given in the first edition of this work. Some writers, as P. de Candolle, Eschweiler, Acharius, and more recently Fuckel, endeavoured to prove the Rhizomorphae to be true Pyrenomycetes, and assigned them perithecia, some of which, according to Tulasne, were in fact merely galls, while others belonged to real Pyrenomycetes, which had grown on or close to the strands of the Agaric. Otth regarded as their fructification a species of Stilbum or Graphium which is sometimes found on old strands in the form of small black bodies of the thickness of a bristle and 3-4 mm. in length and giving off spores by abjunction, a view which was supported by the resem- blance of their structure to that of the rind of the strands, and which after all may in a limited sense still be correct. The question can only be decided by the history of the development of the Stilbum ; but this is not known, and the species may for the present be considered with greater probability to be a parasite on the strands. Other writers, as Palisot de Beauvois, and in more recent times Caspary and Tulasne, looked upon the Hymenomycetes, especially the woody Polyporeae, as the sporophores of the Rhizomorphae, partly because the two were so closely associated in their growth, and partly because these observers confounded the strand-like or membranous mycelia of the former plants with the strands of Agaricus melleus, the characteristic structure of which they did not properly distinguish. Hence Caspary, for instance, brings the Rhizomorphae themselves into genetic connection with the sporophores of quite different species of Polyporus, Trametes Pini, and Agaricus ostreatus. The name Rhizomorpha we now know to be superfluous ; it may and should be dispensed with, as I have myself done above. The same may be said of the name Xylostroma mentioned in the preceding pages, as also of the names Himantia, Ozonium, Hypha, Hyphasma,. Fibrillaria, Ceratonema, all of Persoon, Byssus, Dill. Dematium, Lk. (in part), Corallofungus, Vaill, They were applied, as is well known, since the time of Palisot de Beauvois to sterile mycelial strands which sometimes attained a great size in damp woods, cellars, and mines, but their connection with distinct forms of sporophore, owing to the slight attention which was formerly paid to the study of mycelia, was never actually decided. The forms, which Fries‘ regarded as a distinct genus Anthina, may also be mentioned in connection with sterile mycelial strands of doubtful affinity. The Anthinae, of which I am here speaking, and from which I exclude the section Pterula, Fr. because these appear to be fertile, are cylindrical or ribbon-shaped bodies an inch high on the average and about I mm. in thickness, which grow erect from a floccose mycelium largely developed in decaying wood and leaves, and branch in their upper part dichotomously or in a palmate manner. They are either ofa bright red colour (A. flammea, A. purpurea) or pale brown (A. pallida). They consist of a strand of parallel hyphae firmly united together by a homogeneous connecting substance, and are formed by the union- of the hyphae which spread abundantly through the substratum. The bundle is divided at the upper end, or its hyphae separate from one another and spread on all sides and form the bifurcating or palmate extremities. Specimens are not unfrequently found with the upper end of the plant bent down towards the ground, and there separated into a floccose mycelium or even into net-like anastomoses. I have myself never seen a sporophore in these forms, though Fries says of A. flammea, ‘affusa aqua secedunt sporidia.’ The small cells laterally attached to the hyphae, which I have occasionally found in A. pallida, and which I formerly spoke of as spores, I am now inclined to regard as very doubtful structures. ? Pl. homon. 169. . 30 DIVISION I.—GENERAL MORPHOLOGY. Section VIII. The name sclerotium has been given to certain thick tuber-like bodies formed on the primary filamentous mycelium which proceeds from the ger- minating spore; these, which are storehouses of reserve-material, become detached from the mycelium when their development is complete, usually remain dormant for a considerable time, and ultimately expend their reserve-material in the production of shoots which develope into sporophores. _ The sclerotia are generally exposed on the surface of the substratum, or they are formed on the walls of broad fissures in it or sometimes even in the close tissues of phanerogamous plants. Their form and average size vary much according to the species, the latter being dependent also on the quantity and quality of the food supplied to them. The sclerotia for example of Typhula variabilis are small spheres usually of the size of a mustard-seed, those of Sclerotinia Sclerotiorum differ extremely in shape and may be smaller than a pea or as large as a hazel-nut, or form shapeless cakes some- times an inch in breadth; the sclerotia of species of Claviceps are horn-shaped blunt triangular bodies which may be more than an inch long and some millimetres in thickness, or scarcely 1 cm. in length and 1 mm. in breadth, according to the species and the nutrition. The structure of these bodies in their mature resting state is, in some points of chief importance, the same in all the species. They consist chiefly of a uniform compact tissue, the medulla, which, with a single exception noticed below in paragraph d, is surrounded by an outer layer of peculiar structure forming the rzmd or outer coat. Both parts contain comparatively little water. The medulla is a close weft of hyphae or a pseudo-parenchyma, the elements of which are pale-coloured or colourless and contain a large quantity of reserve food-material ; this in some cases takes the form of a great thickening along with gelatinisation of the membranes of the cells, the lumina of which are narrow and contain little solid matter, as in species of Sclerotinia and in Typhula gyrans, &c., or their cell-walls continue thin and the food-material is in the form of large accumulations of fatty matters, as in Claviceps, or of fine-grained proto- plasmic substances, as in Coprinus stercorarius and others. Exact investigation of the reserve material has been made only in the case of the sclerotia of Claviceps?. The rind is composed of one or more layers of cells which have their membranes wholly or partially sclerosed and dark-coloured, and are poor in solid contents. Within the limits of this general structure, which is common to these bodies, there are special structural arrangements which vary much in the different species. Outward likeness is not always accompanied by agreement in their internal structure, which may also be like or very unlike in nearly related species. The following details, most of which appeared in the first edition of this work, will illustrate these points. a. The sclerotia of the Sclerotinia-Pezizeae (Peziza tuberosa, P. Sclerotiorum, P. Fuckeliana, P. Candolleana, P. ciborioides, P. baccarum, &c.) have a thin, black, smooth or rough rind, and a medulla which in the dry state is of a white or whitish colour. The latter is a firm gelatinous tissue of cartilaginous texture without any * Fliickiger, Pharmacognosie d. Pflanzenreichs ; see before on page 17. CHAPTER II.—DIFFERENTIATION OF THE THALLUS.—SCLEROTIA. 31 - air-conducting passages, as in P. Fuckeliana, or with comparatively few of them. Its hyphae are cylindrical and septate, and interwoven with one another in every direction ; hence in thin sections of the sclerotia their lumina appear in all possible forms according as the section passes through them transversely, obliquely, or longitudinally (Figs. 13, 14). The cells in the moist state contain little else than a watery fluid; in the dry state they contain air. Towards the rind the hyphae are divided into short cells, and in sections therefore most of the cells have a circular outline. The rind consists of isodiametric roundish-cornered cells which have firm dark-brown membranes and adhere closelyto one another. In small forms (Fig. 13) it is composed of one or two layers of cells, in larger (Peziza tuberosa, P. Sclerotiorum, Fig. 14) of three or four or more layers, and then the cells are usually arranged in irregularly radiating rows perpendicular to the surface. It can be easily shown in most cases that the elements of the rind are those segments of the medullary hyphae which lie nearest to the surface of the sclerotium. The breadth of the hyphae varies in different species and sometimes in different individuals. FIG. 13. Piece of a thin transverse section FIG. 14. Thin section through a mature sclerotium of Sclerotinia Sclerotiorum, through asclerotium of Sclerotinia Fuckeliana ; Libert, showing the rind and adjoining medullary tissue. Magn. 375 times. » the rind. Magn. 390 times. 4 Many of the forms which belong to this group occur on the surface of the part of the plant on which they grow, others inside them in their decomposing substance. The- former (Peziza tuberosa, and P. Sclerotiorum frequently) show the structure, which has been described, quite perfectly. Some of the latter, as P. Sclerotiorum, often enclose isolated dead cells or larger portions of the tissue of the part of the plants, which they inhabit, in their own substance, as Corda pointed out. The foreign bodies thus enclosed are irregularly and inconstantly distributed through the medulla, and are sometimes surrounded by a layer of dark-brown cells of the rind. The smaller sclerotia of this type, which are found growing on decaying leaves (Peziza Candolleana, Lev., P. Fuckeliana), regularly take possession of the substance of the leaf at the points where they are developed. They are weal-like swellings on the leaf, formed of the tissue-elements of the sclerotium, among which the dead elements of the leaf are interposed, though more or less displaced and separated from one another. The way in which the sclerotium takes possession of the tissue of the leaf is different in different species. The sclerotium of P. Fuckeliana for example (Fig. 19) inhabits only the parenchyma and epidermis of the leaf of the grape-vine, but sometimes it grows even over the hairs on the leaf and so appears 32 DIVISION I.—GENERAL MORPHOLOGY. to be spikey ; it often appears along the veins of the leaf, but always outside the wood-bundles; I found the sclerotia of P. Candolleana on oak-leaves, but there also only in the parenchyma. But the sclerotium of a small Peziza which inhabits the leaves of Prunus insinuates itself among all the elements of the veins of the leaf. é. The structure of the sclerotia of several of the Hymenomycetes, especially Agaricus cirrhatus, P. (?), A. tuberosus, Bull., and Hypochnus centrifugus, Tul., differs little from that of the first type. The chief difference is that the cell-walls in the rind are not a dark but a yellow brown; the surface of the rind is in most cases tolerably smooth, but in Hypochnus centrifugus it is uneven or felted over with the remains of the hyphae which surround the sclerotium in its younger state. The hyphae of the medullary tissue and their membranes are of varying thickness according to the species; they are in most cases chiefly filled with a watery fluid or with air; in Hypochnus centrifugus they contain drops of oil. I have never found tissue-elements of the host enclosed in the medulla even of those of the above mentioned sclerotia, which had developed in the interior of decomposing parts of plants (Mushrooms). c. A somewhat different structure from the above is seen in a sclerotium in Rabenhorst’s Herb, mycol. Nr. 1791, incorrectly named Sclerotium stercorarium, and of doubtful origin. Its white medullary tissue consists of thin-walled cylindrical hyphae which contain a watery fluid, and are usually rather loosely interwoven, the interstices being filled with air. Towards the surface the medulla passes gradually into an outer covering of many layers of narrower hyphae, which mostly run_ parallel to the periphery and form a tissue without interstices. The inner layers of this tissue are colourless, towards the outside the membranes become gradually yellow- brown, and those of the outermost layers are so considerally thickened that the lumina are much reduced in size. The whole sclerotium is thus surrounded by a firm uneven rind composed of several layers. ad. The light-yellow Sclerotium muscorum, which also belongs to some Agaric, consists of a web of broad thin-walled hyphae with narrow interstices containing air. The hyphae, which are not arranged in any order, are composed partly of elongated cylindrical and partly of short vesicular cells. The latter contain a clouded homo- geneous yellowish protoplasm, or a watery fluid in which drops of yellow oil are suspended. The surface of the sclerotium appears to the naked eye of a darker colour than the centre, but under the microscope the structure is seen to be the same throughout, and the medulla and rind are not clearly distinguished. Single surface-cells project here and there as cylindrical papillae. e. The snow-white medulla of the sclerotium of Coprinus stercorarius, Fr. has a similar structure to that in Sclerotium muscorum. It is a pseudo-parenchyma composed of broad irregularly roundish or elongate-ovoid cells and single cylindrical hyphae; all the cells are very thin-walled and filled with a colourless, uniformly and finely granular, somewhat strongly refractive protoplasmic substance, which issues forth from injured cells and spreads through water and makes it turbid. These cells form a close tissue which is hard in the dry state, and has more or less narrow interstices filled with air. The cells of the medulla become suddenly smaller towards the circumference. The surface of the sclerotium is formed of a firm apparently black rind which is wrinkled in the dry state. Where this rind borders on the medulla it shows four or five irregular layers of small cells of the shape and size of the outermost cells of the medulla, but with brown membranes and apparently always clear watery contents. This layer is surrounded by the more superficial rind consisting of three or more layers of large cells usually of irregular roundish outline, which at the periphery have some resemblance to the largest of the cells of the medulla, and contain a watery fluid or air within a slightly thickened wall of a dark violet-black colour. Many of the superficial cells of the rind project irregularly above the rest CHAPTER IJ,—-DIFFERENTIATION OF THE THALLUS.—SCLEROTIA. 33 and some are prolonged into short irregular hairs or papillae, while in others the membrane is irregularly torn on the outer side of the cell and the exterior surface is thus rendered rough and uneven. sf. The sclerotia of some Typhulae, T. phacorrhiza, T. gyrans, T. Euphorbiae, Fuckel, T. graminum, Karst., &c. have the gelatinous medulla with cartilaginous consistence of the type a, with slight differences as regards the thickness and firmness of their membranes in the several species. The hyphae contain a clear watery fluid which sometimes has granules sparingly distributed through it; in T. graminum only they are densely filled with homogeneous turbid protoplasm. The rind in these species is a single layer of cells of uniform height connected by their sides without interstices, which are evidently the peripheral segments of the medullary hyphae, unlike them as they may be in structure. The cells are tabular or shortly prismatic in shape, their lateral walls often curved and sinuous ; the inner and lateral walls are slightly, the outer walls very strongly thickened in the manner of the outer wall of the epidermal cells in vascular plants, and have their outer surface smooth (Fig. 15 c) or warted (Fig. 15 a, 6). The rind is thus remarkably like the firm epidermis without stomata of many vascular plants. g. In the sclerotia of Typhula variabilis, Riess, and Peziza Curreyana the structure of the rind is essentially the same as in the last type, but the white or in P. curreyana the rose-red medullary tissue is a weft of cylindrical hyphae with ff Wie 4 y My, FIG. 15. @ and 4 sclerotium of 7yphula phacorrhtza. a piece of a thin transverse section ; »—r rind-cells, g—g outer layers of the same. 4 piece of the rind flattened out, seen from the outside ; at s the outside of outer layers only is seen without the lateral walls of the cells. c¢ cortical layer of the sclerotiuin of 7yphula gyrans flattened out and seen from the outside, Magn. 390 times. air-spaces. The hyphae are thin-walled in Typhula with dense, granular contents ; in P. curreyana the membrane is thickened and stratified, and the medullary tissue is more compact towards the periphery as is the case in type a. h. The sclerotia of species of Claviceps, the blunt trilateral horn-shaped bodies which develope in the flowers of the Gramineae and Cyperaceae at the expense of the ovary and are known by the name of evgo¢, consist in the mature state chiefly of a dirty-white medullary tissue surrounded by a violet-brown rind. The medulla has the character of:a pseudo-parenchyma formed of cylindric prismatic cells, which are on an average from one to four times as long as broad. The cells are arranged in straight or sinuous longitudinal rows, and the history of their development shows that they possess the characters of the fungal hyphae. This may also be clearly seen even in ripe sclerotia, in the interior of which clefts and fissures are often found clothed or loosely filled with a thin felt ; sections show that the felt is composed of interwoven hyphae, which spring as branches from the rows of cells of the compact tissue and have the same characteristics, except that their weft is looser. The medulla has usually shorter and broader cells towards the periphery of the sclerotium than in its centre. The cells are everywhere provided with tolerably thick colourless membranes, and are usually firmly grown ‘together on every side without interspaces. They contain large colourless drops of oil. [4] D 34 DIVISION I,.—-GENERAL MORPHOLOGY. The medulla is surrounded at first by an inner stratum of the rind which is at every point firmly connected with it, and is composed of one or two layers of cells with contents showing no oil, and with membranes that are strongly thickened often more on the outside than on the inside and of a dark violet-brown colour. This inner stratum of the rind is enclosed by an outer portion formed of a few or even as many as twenty layers of longitudinally arranged or irregular branched rows of cells; the cells are narrow and their membranes are of a pale violet-brown. This is the thin pale-violet coating, often with longitudinal stripes or interruptions, which clothes the surface of the fresh sclerotium and may be easily broken or rubbed off from the firm inner rind. All sclerotia, it would appear, develope as secondary formations on a primary sporogenous filamentous mycelium. They arise from a single branch of a mycelial filament which has quickly produced a tuft of many branchlets; this is the case in Coprinus stercorarius, Typhula variabilis, and T. gyrans. In others, as in the forms of Sclerotinia, several adjacent branches of the primary mycelium take part in the forma- tion from the first. In both cases the young sclerotium soon rises above the substratum as a small tuft of loosely tangled hyphal branches in all essential points similar to the primary. Then in Sclerotinia Sclerotiorum the filaments of the tuft grow vigorously and branch and coalesce repeatedly by means of H-shaped cohesions, and thus the tuft itself developes into a dense white ball of the size of the sclerotium ; till this size is reached, the structure of the hyphae remains as it was originally, the new branches are often slenderer than the primary hyphae and their character is uniform in all parts of the ball. The interstices in the tissue contain air, the surface is rendered finely hairy by the presence of slender spreading branchlets of the hyphae, and the whole body.is soft and can be easily compressed into an extremely small compass. But from this time by new formations in its interior, and afterwards by expansion of the cells already formed, the tissue constantly increases in size and firmness. Lastly the thickening of the membranes commences, which is characteristic of the species, and this is accompanied with a partial disappearance of the air-spaces and the differentia- tion into medullary and cortical layers. This process of development begins in the interior of the tissue and advances rapidly towards the circumference. The outermost layer of the white ball takes no part in it, but remains for a time as a white felted covering on the rind which is distinct from it, and ultimately shrinks to nothing and disappears. The ripe sclerotium becomes detached from its felted environment as a body of sharply defined form and outline. - Sclerotinia Fuckeliana exhibits the same phenomena when cultivated upon a microscopic slide; but, as might be expected, these are modified by the nature of its environment when the sclerotium is developed spontaneously inside the tissue of a phanerogamous plant. Peziza ciborioides also behaves in a similar manner, but shows some specific variations in its development. The tuft of hyphae which is the commencemet of a sclerotium of Typhula variabilis rises above the substratum in which the primary mycelium has spread its ramifications’. The branches of the tuft become woven together into a smooth white spherical body of small size, which is attached to the substratum by a short and slender stalk. The sphere enlarges rapidly by the formation of new cells and 1 The substratum in the natural way of growth is formed of decaying leaves in winter and spring ; Brefeld employed nutrient solutions for the purpose of artificial culture. CHAPTER II.—-DIFFERENTIATION OF THE THALLUS.—-SCLEROTIA, 35 branches in all its parts. It is entirely formed at first of uniform thin-walled much branched hyphae, which are rich in protoplasm and closely woven together, but not without air-spaces. Those parts only of the hyphae which form the outer moist surface of the sphere have no interstices between them ; if we examine a sclerotium in a very early stage of its development we see that the surface is formed ofa layer of short cells of uniform height, which are segments of hyphal branches running in numbers through the periphery. These cells are at first thin-walled and filled with protoplasm, like the other portions of the hyphae, and their walls are colourless. Growth by formation of new hyphal branches continues for some time longer in the centre of the sphere, and thus the medulla enlarges its circumference considerably, while its hyphae grow to twice their original size ; but the intertwining of the hyphae remains as it was before. From an early stage in the development no new cells are introduced between the previously existing cells of the superficial layer ; but these cells stretch in every direction, and sufficiently strongly in that of the surface of the sphere to remain united together into a layer without interstices. Their radial or lateral walls assume in this way the undulated inflated outline mentioned above in paragraph f while their outer membrane becomes thickened to form the covering described in the same place, and takes the permanent yellow colour or passes through yellow and brownish yellow to a dark brown; the protoplasm disappears. This formation of rind is continued also at the point of insertion of the stalk over a layer of cells which lies in the direction of the surface of the sphere, and the sphere is thus divided off from the stalk and is ultimately detached from it, while the stalk dries up. The development of Typhula gyrans follows a similar course. All that is known of the development of other sclerotia, excepting that of Claviceps, agrees with the processes above described, though the final differentiation is accompanied by certain variations in detail, as will be inferred from the statements in paragraphs @ to g; in this matter Brefeld’s careful description of Coprinus stercorarius should be’ consulted. $ The sclerotia, of the development of which we have been speaking, are not all formed on morphologically definite spots of the primary mycelium, and their number varies according to the state of its nutrition. When several begin to be formed near each other, they may unite as they grow into one body; this leads to the formation of the irregular cakes and crusts mentioned above, especially in - Peziza Sclerotiorum, though it is observed in other species also, as in Coprinus stercorarius, and in a less degree in Typhula gyrans. Much water is expelled from all the above sclerotia when the differentiation and final development commence in them, and appears on their surface in large clear drops. The whole process of development may under favourable conditions be accomplished from beginning to end in a few days. The sclerotia of Claviceps (ergot), concerning which Tulasne’s labours have given us more exact information, show several variations of detail in their development arising from the peculiar parasitism of the Fungus (Figs. 16,17). The primary mycelium occupies at first the base of the young ovary in the flower of the Gramineae and Cyperaceae. In ordinary cases, to which we will at present confine our attention, it spreads rapidly through the entire ovary, with the exception of its apex and some- times also of the inner layers of its wall; the ovary is thus changed into a white Fungus-body of nearly its own shape, with a surface marked with deep narrow D 2 36 - DIVISION I,—GENERAL MORPHOLOGY, curved furrows ; and as gonidia are formed on the surface in a way that will be after- wards described (see Division II) the body may be termed a gonzdiophore (Fig. 16). The hyphae of the Fungus-body must necessarily make their way for some distance from the ovarian base into the floral pedicel, for it is difficult to conceive of any other mode of supplying food to the Fungus; but we have no exact information on this point. When the gonidiophore is fully formed, the beginning of a sclerotium makes its appearance in the torus at its base and on the mycelium, which is supposed to spread through it, in the form of a small somewhat elongated fungal body enclosed in the white tissue and distinguished by its greater density (Fig. 16 4, s). It is formed at first of slender delicate separable hyphae which are continuous with those in the vicinity, but are somewhat firmer and more closely compacted. Its FIG. 16. Claviceps purpurea, Tul. @ young ovary of Secale cereale penetrated and covered with the gonidio- phore, seen from without; the hairs of the ovary and the remains of the style g project at the apex from the fungal investment. 4 longitudinal section through a similar stage FIG. 17. Claviceps purpurea, Tul., on Secale cereale. @ seen from without. 4 median longitudinal section. The sclerotium s rests on the torus and carries up the dry- ing gonidiophore / on its apex. After Tulasne, Slightly magnified, — in the development from Seca/e; s commencement of the sclerotium. c similarly young state of the Fungus on the pistil of Glyceria fluztans, the Fungus projecting beyond the apex of the ovary. After Tulasne. Slightly magnified. surface soon acquires a violet hue, the superficial cells beginning to assume the character of the future rind. It now increases in thickness and elongates into the well-known horn-shaped body, which is attached at its base to the torus and projects above from between the paleae. The course of its development still requires more exact investigation. Its growth in the longitudinal direction is no doubt maintained by continued addition at the base. The increase in thickness of each transverse section above the base must, in a great measure be due to the expansion of cells already formed, since these are more than four times broader in the fully developed parts than in the younger. The gonidiophore ceases to grow as soon as the sclerotium begins to be formed, and being detached from the torus as the sclerotium enlarges it is carried up like a cap on its apex, and there shrivels up and sooner or later falls off (Fig. 17). CHAPTER II,—DIFFERENTIATION OF THE THALLUS,—-SCLEROTIA. 37. The development of these sclerotia is slow; it required for instance about four weeks, according to Tulasne’s observations, in the months of July and August in the flowers of Brachypodium sylvaticum. In this case, when the sclerotia began to develope, drops of a saccharine fluid were observed to appear; but it is uncertain to what extent they were connected with the formation of the sclerotia or with that of the gonidia. It sometimes, but rarely, happens that the Fungus is developed beneath the point of attachment of the ovary; when this happens the ovary preserves its proper form and is carried up between the paleae on the apex of the sclerotium, and there withers away before its time. The sclerotia when fully formed and matured pass into a resting state, the duration of which varies in species and in individuals with external and internal causes, as is the case with seeds, tubers, and rhizomes. It depends on the habits of life of the species in the natural condition whethet the period of rest is confined for example to winter, as is the case with Claviceps, Peziza Curreyana, and P. Duriaei, or to summer, as in Typhula gyrans, T. variabilis, and T. phacorrhiza, or is not constantly connected with the time of year. In the former case the time of rest may only be slightly shortened in some species by changing the external conditions, as the example of Claviceps especially shows. Sclerotia if kept dry will retain their power of development for a long time unimpaired ; those of Peziza Sclerotiorum for more thana year, according to Brefeld for several years, those of Claviceps for about a year; after about that time those of the latter species and of Peziza Fuckeliana also usually lose their vitality. The external conditions for the further development of the sclerotia are the ordinary general conditions for germination, sufficient supply of water and oxygen anda suitable temperature. The usual procedure under such conditions is as follows. The sclerotium first absorbs water and swells, and then in a longer or shorter time, often not till after some months, it sends out shoots at the cost of the food-material stored up within it, and these develope directly into the sporophores characteristic of the species. The sporophores in the species which form sclerotia, with the exception which will be named further on, are compound structures. They accordingly make their appearance as bundles of hyphae springing as branches from the elements of the sclerotium, and in two ways according to the species. In one case (Figs. 18, 1g) represented by Claviceps, Sclerotinia Fuckeliana and S. Sclerotiorum; Typhula gyrans and T. phacorrhiza, the bundle of hyphae arises at a certain spot in the medullary tissue and from branches of it which originate beneath the rind ; the latter has no share in the new formations but is pierced through by the advancing bundle of hyphae. A more minute description of the special circumstances observed in Sclerotinia will be given in Division II. In the second case the bundle of hyphae is formed by the ramification of outgrowths from the cells of the rind, as Brefeld rightly states in the case of Coprinus stercorarius ; whether it is always a single cell that produces these shoots must for the present remain undecided. Agaricus cirrhatus also shows this formation. Typhula variabilis is in some respects intermediate between the two cases ; here according to Brefeld the initial bundle of hyphae appears on the surface of the rind, neither springing apparently from a cell of the rind, nor causing an evident broad 38 DIVISION I,—GENERAL MORPHOLOGY. fissure in the rind, and formed therefore in all probability from a single branch proceeding from a peripheral medullary hypha and piercing through the rind. The exceptional case mentioned above, in which the product of the sclerotium is not a compound structure, is the formation of simple filamentous gonidiophores, known by the name of Botrytis cinerea, from the sclerotia of Peziza Fuckeliana. In most of the cases which I have myself examined a bundle of hyphae shoots out from the subcortical medullary region, and where it has broken through the rind the hyphae spread in different directions, and each developes into a gonidiophore. But it sometimes happens that the cells of the rind develope directly into gonidiophores. In none of the sclerotia that have been examined is the origin of the shoots connected with a definite predestined morphological spot. Any fragment of the larger sclerotia, if not too small, can under ordinary circumstances produce them, as Tulasne showed in the case of Claviceps, and Brefeld especially in that of Coprinus stercorarius. The number also of the shoots that may proceed from a sclerotium is not definite in any species ; and some species can produce an almost unlimited number G FIG. 18. a and ¢ Claviceps purpurea, b C. microcephala,T. aand éscle- FIG. 19. Sclerotinia F'uckeliana, a very rotia with mature sporop c transverse section through a sclerotium small specimen. s transverse section through with the young sporophores emerging from the interior. After Tulasne, ¢ a sclerotium, from which a sporophore cut and 6 nat. size, c slightly magnified. through lengthwise has proceeded. The dark spots in the sclerotium are the dead cells of the vine-leaf which it has occupied; the spots and dots at fg are calcium oxalate aggregations. Magn. 20 times. of these primordia (Anlagen) of sporophores on their sclerotia, others cannot do this. Vigorous specimens of Coprinus stercorarius, according to Brefeld,. may produce hundreds of primordia, of which however few are ever perfected, and if those already formed are intentionally and repeatedly destroyed hundreds of fresh primordia as repeatedly make their appearance. Other species are less productive; Sclerotinia Sclerotiorum seldom has two dozen sporophores even on strong plants; species with small sclerotia have usually one only or very few. The size of the individual sclerotia on one and the same species, other conditions being the same, generally causes a difference in the number of the sporophores which commence and complete their development, and in the vigour of growth of the _ latter. Larger sclerotia are on the whole more productive than the smaller. Claviceps purpurea produces 20-30 sporophores from such large sclerotia as are formed upon the ears of Secale cereale, but only one or a few weakly ones from the small sclerotia upon the spikelets of Bromus, Lolium, and Anthoxanthum. Similar differences arising from the size of the sclerotia are observed also in Sclerotinia Sclerotiorum and in Coprinus. The relation between size and productiveness is the CHAPTER II,—DIFFERENTIATION OF THE THALLUS.—SCLEROTIA. 39 same in fragments of a sclerotium as in their corresponding sclerotia. It is natural to assume, without closer inquiry into the metabolism, that the cause of these phenomena lies in the difference in quantity of the reserve-material at the disposition of the plant according to the size of the sclerotia or their fragments, and that the not infrequent irregularities and apparent exceptions to the rule are due, other things being equal, to differences in quantity or quality in the reserve-material, which may occur also, be it remembered, where the size of the sclerotia or of its fragments is the same. The formation of the primordia and the further development of the sporophores is accompanied by the solution, transformation, and consumption of the food-material stored up in the sclerotia. The process begins at the point of origin of a primordium and spreads by degrees through the medullary tissue. In Claviceps, according to Tulasne, the oil disappears and its place is taken by watery fluid, the cell-membranes become thinner and ultimately very delicate, and the cells separate readily from one another. In the sclerotia of Sclerotinia Fuckeliana, S. Sclerotiorum, S. tuberosa, Typhula gyrans, &c. which are gelatinous witha cartilaginous consistence, the gelatinous thickening-layers of the hyphae become softer and pale and by degrees scarcely recognisable, so that the innermost layer only of the membrane can still be clearly seen as a delicate pellicle. The former firm union of the hyphae naturally comes to an end at the same time ; and a mass of granular matter which turns yellow with iodine collects in the cavities of the cells, and diminishes again in quantity as the sporophores increase in number _and size. In Coprinus stercorarius, according to Brefeld, the granular protoplasm of the cells is replaced by a watery fluid, and the membranes become pale and undistinguishable. Ultimately in all these cases the medullary tissue almost entirely disappears. The rind at first takes no perceptible part in these changes ; it remains behind after the disappearance of the medulla as a soft sac which collapses and decays. These processes take a longer or a shorter time in different cases. In Brefeld’s culture of Coprinus stercorarius they were over in 7-10 days. In most species they take much longer time. Sclerotinia Sclerotiorum, for instance, may put out new sporophores one after anotlier during some months from one sclerotium, and develope them slowly before the supply of food is exhausted. I have found sclerotia of Agaricus cirrhatus {see on page 37), which had developed one or more sporophores and fully matured them, not sensibly different in consistence and structure from others which had not yet produced any; they might therefore repeat the production of successive sporophores and perhaps during a considerable time ; but this point remains to be determined. Some. sclerotia, as those of the Sclerotinieae, of Coprinus stercorarius and Claviceps, are able in the mature state and as long as they retain their vitality to form new rind over wounds, such as cut surfaces which reach to the medullary tissue, provided they are exposed to the air but are protected from desiccation. The new rind resembles the old ordinary tissue in all essential points. It is formed by the medullary hyphae exposed by the wound sending out branches, which become woven together into a delicate felt and cover the surface of the wound. The inner layers of this covering which are next the uninjured medullary tissue then develope into a new rind, while the outer ones dry up and disappear. If such wounded places are kept in a.nutrient solution, the branches put out by the medullary hyphae on the exposed points may, in the Sclerotinieae at least, develope into vegetating mycelial hyphae 40 DIVISION I.—GENERAL MORPHOLOGY. instead of forming new rind. The sclerotia of the Typhulae in which the tissues are very distinctly differentiated appear not to be capable of these acts of regeneration. The following remarks are intended to illustrate and complete what has been stated above. ‘ The production of the primordia of sporophores from the cells of the rind of Coprinus stercorarius is given on the authority of Brefeld. It is not strange in | itself, even in presence of the facts illustrated in Figs. 18 and 19, that the superficial cells of the sclerotium should remain capable of further development and of branching, and that the ordinary distinct division of labour between the protecting rind and the medulla should in some cases not be observed. There is therefore no antecedent difficulty in admitting a third mode of production such as Brefeld gives in the case of Sclerotinia Sclerotiorum, in which the medullary cells and cells of the rind both par- ticipate. But I have not admitted this case into my account because the facts will not bear this interpretation. Young shoots always spring in this species from the medulla in the peculiar manner which will be described in Division II, and burst through the rind to reach the surface. In somewhat older specimens, such as those which are very beautifully and correctly portrayed in Brefeld’s Table viii. Fig. 9, the true state of the case is obscured by the circumstance that the superficial cells of the sporophore from the point of emergence are very like those of the rind of the sclerotium in shape and in their dark colour, so that the new cells appear to be directly continued into the superficial cells. Thin sections even in more advanced states of growth under sufficient magnifying power show that the case is as I have stated it, and exhibit clearly the arrangement of the black superficial cells, which are the extremities of hyphal branches proceeding from branches of the emerging tuft of hyphae and passing to the surface in diverging curved directions. That the shoots from the sclerotia in the cases described above should always have been termed primordia of sporophores requires no special explanation, even in the case of Sclerotinia Sclerotiorum where they may under unfavourable circumstances develope in the ground into long branched strands. Even the normal sporophores of this Peziza may be branched, and the branches of the strands may under favour- able conditions of development revert to the normal sporiferous state. Brefeld indeed saw them on several occasions produce a filamentous mycelium which subsequently formed sclerotia ; but these are monstrous developments such as occur also elsewhere, the exceptional cases that confirm the rule. It is true that phenomena have been reported in connection with the formation of shoots from sclerotia, which vary from the descriptions in the text; but more searching investigation is needed in all these cases. Thus Tulasne saw sclerotia of Hypochnus centrifugus, which had been placed in damp sand in the end of April, produce in August and September a filamentous mycelium like a spider’s web, which subsequently developed the ordinary sporophores of Hypochnus. As regards the connection of the mycelial hyphae with the sclerotium it is merely stated that they spread in every direction from its surface. The consistence and structure of the sclerotia remained unchanged after the production of shoots; hence Tulasne rightly considers our knowledge of them as not yet complete. Tulasne has already pointed out that Léveillé’s older statement, that a floccose mycelium is first produced from the sclerotia of Agaricus grossus, A. stercorarius, A. racemosus, and A. tuberosus, and afterwards sporophores from the mycelium, is founded on a mistake. Another exceptional occurrence, demanding more critical investigation, is described by Micheli? as taking place in Peziza Tuba, Batsch, a species which seems scarcely to have been examined since his time. The sclerotium as it lies in the ground puts + Nova plantarum genera (1729), p. 205, ‘ Fungoides, No. 5.’ CHAPTER II,—DIFFERENTIATION OF THE THALLUS.—SCLEROTIA. 4I forth a number of erect sporophores in the spring, and forms a new sclerotium destined to produce sporophores in the succeeding year. The exhausted sclerotium of the previous year is usually still in existence when the new one is formed, so that the underground portion of the Fungus consists of three small tubers of unequal size. Historical remarks. Although it has long been known that the sporophores of certain Fungi, species of Typhula and Agaricus and some others, are developed from small tuber-like bodies, our more exact knowledge of the nature of the sclerotia is derived from an excellent publication of Léveillé which only appeared in 1843, and even this work attracted little notice till Tulasne again called attention to the subject and threw new light upon it by his work on Claviceps in 1853. Up to that time the greater part of the sclerotia were considered to be independent representatives — of distinct species, and the name Sclerotium was introduced by Tode? to designate the genus formed by the supposed species, each with its own specific name. Some fifty species of Sclerotium were described by Fries in his Systema mycolo- gicum and his Elenchus; the number was subsequently increased to eighty and ° additions to it are still made by writers, who prefer the hasty publication of imperfect observations to more prolonged investigation. It appears, as has been shown above, that we are at the present time acquainted with the development and especially with the sporophores of a considerable number of sclerotia. Others are less perfectly known, in some only the mature sclerotium has been seen. Undescribed sclerotia are still not unfrequently found in examining Fungi. Appended is a list of the species of Fungi which are at present known or supposed to form sclerotia, together with the old specific names of the sclerotia wherever they have been ascertained. 1. Peziza tuberosa.—P. Tuba, Batsch (Micheli, l. c.), P. Sclerotiorum, Lib. Sclero- tium compactum, S. varium), P. Candolleana, Lev. (Sclerotium Pustula), P. Fuckeliana (Sclerotium echinatum, Fuckel) ; the two last named Pezizas are in all probability iden- tical, and to them belong the gonidiophores known as Botrytis cinerea, P. (B. erythropus, Lev.), and the ‘Sclergtium durum’ from which these spring. The little Peziza men- tioned in par. a, p. 32, as growing on the veins of the leaves of Prunus is very near to these species; its sclerotia found on the same leaves were incorrectly named Sclerotium areolatum, Fr. in my first edition. Peziza ciborioides, Fr. (Hoffmann).—P. baccarum (Schrdter). P. Curreyana, Berk. (Sclerotium roseum, Kneiff). P. Durieana, Tul. (Sclerotium sulcatum, Desm.). The above Pezizas with some others have been made a separate genus Rutstroemia, by Karsten (Mycol. fennica) and Sclerotinia by Fuckel (Symbol. mycolog.). Peziza ripensis, Hansen. 2. Claviceps purpurea, Tul., C. microcephala, Tul., C. nigricans, Tul. (Sclerotium Clavus, DC:).—C. pusilla, Cesati. Hypomyces armeniacus, Tul. Vermicularia minor, Fr., also Xylaria bulbosa, P. (see Tul. Carpol.). 3. Typhula lactea, Tul.—T. Todei, Fr.—T. caespitosa, Ces.—T. Euphorbiae, Fuckel (Sclerotium Cyparissiae, DC.?), T. graminum, Karst. (Sclerotium fulvum, Fr.), T variabilis, Riess (Sclerotium Semen, Tode if the cortex is dark-brown, Sclerotium vulgatum, Fr. if it is yellow).—T. erythropus (Sclerotium crustuliforme, Dsm.).—T. phacorrhiza (Sclerotium scutellatum, A. S.).—T. gyrans (Sclerotium complanatum, Tode). I give the names if the two last species on the authority of Fries, Hymeno- mycetes Europaei, 1874. Léveillé had given the name of Clavaria juncea to the sporophores growing out of Sclerotium complanatum, and in my first edition I gave * Fungi Mecklenburgenses selecti, p. 2. 42 : DIVISION I.—GENERAL MORPHOLOGY, - the names Clavaria complanata and C. scutellata after the sclerotia to the two species which are scarcely distinguishable except by the sclerotia, Pistillaria micans (Sclerotium laetum, Ehr.).—P. hederaecola, Ces, Clavaria minor, Lév. (which also belongs to Typhula). 4. Hypochnus centrifugus, Tul. 5. Coprinus stercorarius, Fr. (Sclerotium stercorarium), C. niveus, Fr. (Hansen.) Agaricus racemosus, P. (Sclerotium lacunosum).—A. tuberosus, Bull. (Sclerotium cornutum).—A. cirrhatus, P.(?) is the name which I have given above to the small white Agaric which grows from Sclerotium-fungorum. Other Agarics are also said to form sclerotia: A. tuber regium, Fr., A. arvalis (Sclerotium vaporarium).—A. grossus, Léy., A. fusipes, Bull., A. volvaceus (from Sclerotium mycetospora, Nees in Nov. Acta Nat. Cur. XVi, 1), &c. Sclerotium pubescens, P., Sclerotium truncorum, Fr. were supposed to be connected with such Agarics, on which point see Léveillé and Tulasne. The statements and determinations are many of them doubtful, and more accurate investigations are required. 6. Tulostoma pedunculatum, Tul. (Schréter). There are a large number of tuber-like compound Fungus-bodies the real character of which is still doubtful; our ignorance of their structure or development makes it impossible to decide whether they are sclerotia or some other formation. Among these are Pietra fungaja of South Italy, which is formed of the mycelium of Polyporus tuberaster, Jacq. rolled up into solid masses with bits of soil, stones, and the like; and the tuberous fungoid bodies named Mylitta, Sclerotium stipitatum, Berk., Sclerotium Cocos, Schweinitz, which grow beneath the surface of the ground to the size of a fist. or a head and are known only in the sterile state, with some others. Swellings in the substance of phanerogamous plants such as the tubercles on the roots of the Leguminosae, which were once mistaken for sclerotia, require no further notice here. Section IX. Besides the sclerotia which have been described above with well-marked characters morphological and biological there is a motley assemblage of compound Fungus-bodies, which approach the sclerotia in their biological character, — but cannot be classed with them from a strict morphological point of view. Such bodies may be termed sclerotioid, or, for brevity’s sake, simply sclerotia, if we do not thereby infer their identity with true sclerotia. The biological agreement between these bodies and sclerotia consists in similarity of structure, in their being storehouses of reserve-material and in their normally passing through a period of rest, after which they proceed to a further development. Morphologically they are 1. Transitory resting stages of mycelia, which under favourable circumstances again develope into filamentous mycelia. Such are the small fatty tubers which are the resting stage of the mycelium of Hartig’s Rosellinia quercina, and perhaps for- mations like Sclerotium Cocos and others mentioned above as of doubtful character. 2. Perithecia, which when developed enter upon a long period of rest, and assume at the same time the form and structure of a sclerotium; these do not ultimately produce sporophores, but develope in their interior the asci, which are the charactéristic organs of reproduction in perithecia. Of this kind are some — species of Pleospora- and Penicillium, which will be fully described in Division II. The ‘sclerotia’ of the Aspergilli of Wilhelm are certainly homologous with the perithecia of Penicillium and are also biologically analogous with them. - 3. The bodies, which may still retain the old name of xyloma, and which differ for the most part from sclerotia only in their less definite shape and outline, and in CHAP, II.—DIFFERENTIATION OF THE THALLUS,-+ SCLEROTIOID BODIES. 43 not sending out sporophores as branches, but in producing sporogenous receptacles in their interior. Well-known examples are the Ascomycetes of the genera Rhytisma, Polystigma, Phyllachora and many of their allies which live on leaves. They develope in the substance of the leaves, which they attack during the summer, a thallus very closely resembling in many respects the sclerotia of Sclerotinia Fuckeliana, and primordia of sporogenous receptacles are formed at the expense of the reserve-material in the interior of the thallus after it has passed the winter on a dead leaf; examples of these will be described in greater detail in Division II. ‘Literature of mycelia. Filamentous mycelia, haustoria, &c. See the lists of authors under the several genera and groups in Division II. Erisyphe :— v. MOHL in Bot. Ztg. 1853, p. 585. DE Bary, Beitr. zur Morph. u. Phys. d. Pilze III. Mycelial strands. Xylostroma, &c. :— ROSSMANN, Beitr. z. Kenntn. d. Phallus impudicus (Bot. Ztg. 1853, Nr. 11). TULASNE, Fungi hypogaei, p. 2 (Fungor. Carpol. I, pp. 99, 120, &c.). H. HOFFMANN in Bot. Ztg. 1856, p. 155. PALISOT DE BEAUVOIS in Ann. du Mus. d’hist. nat. VIII (1806), p. 334. DUTROCHET in Nouv. Ann. du Mus. dhist. nat. III (1834), p. 59. TURPIN in Mém. de l’Acad. d. Sc. XIV (1838). (Turpin and Dutrochet both describe the development of Cantharellus Crucibulum, Fr. from a reticulately branching mycelium.) FRIES, Plantae homonemeae, p. 213. LEVEILLE in Ann. d. sc. nat. sér. 2, XX, p. 247. DE Bary, Ueber Anthina hed wie I, p. 35) ;—Id. Beitr. z. Morph. u, Phys. d. Pilze I (1864). JUNGHUHN in Linnaea, 1830, p. 388. R. HARTIG, Wichtige Krank. d. Waldbaume, Berlin, 1874, p. 46 ;—Id. Die Zerset- zungserscheinungen d. Holzes, Berlin, 1878. Rhizomorphae. (See also Streinz, Nomenclator. Bail, Tulasne, II, cc., Palisot de Beauvois, 7. ¢.) :— EHRENBERG, De Mycetogenesi, 7. c. p. 169. ESCHWEILER, Commentatio de generis Rhizomorphae fructificatione, Elberfeld, 1822. NEES v. ESENBECK in Nov. Act. Ac. Nat. Curios. XI, 654; XII, 875. J. SCHMITZ, Ueber d. Bau &c, d. Rhizomorpha. fragilis, Roth. (Linnaea, 1843, p. 478, tt. 16, 17). TULASNE, Fungi hypogaei, p. 187 ;—Id. Fungor. Carpol. I. BAIL in Hedwigia I, 111, and Ueber Rhizomorpha und Hypoxylon in Nov. Act. Ac. Nat. Cur. Bd. 28 (1861). LascuH, Bemerk. iiber Rhizomorpha (Hedwigia I, 113). OTTH, Ueber d. Fructification d. Rhizomorpha (Mittheilangen d. Naturf. Ges. Bern, 1856). v. CESATI, in Rabenh. Herb. Mycol. Nr. 1931. CASPARY, Bemerk. iiber Rhizomorphen (Bot. Ztg. 1856, p. 897). FUCKEL in Bot. Ztg. 1870, p. 107. | ‘ R. HARTIG, Wichtige Krankh. d. Waldbaume, 1874. BREFELD, Unters. iiber Schimmelpilze III, 136. 44 DIVISION I,—GENERAL MORPHOLOGY. Sclerotia :— DE CANDOLLE in Mém. Mus. d’hist. nat. II, 420. LEVEILLE, Mém. sur le genre Sclerotium (Ann. sc. nat. sér. 2, XX). CorDA, Icon. fung. III. TULASNE, Mém. sur l’Ergot des Glumacées (Ann. sc. nat. sér. 3, XX, 1853). KUHN, Krankh. d. Culturgewachse, p. 113, t. V. (A list of the many treatises on the sclerotium of Claviceps = Secale cornutum or ergot, will be found in Tulasne, |. c. and in Handbooks of Pharmacognosy ; earlier ones in Wiggers, Dissert. in Secale cornutum, Gottingen, 1831.) TULASNE in Ann. d. sc. nat. sér. 4, XIII (1860), p. 12 ;—Id. Select. Fungor. Carp. Cap. VIII. ; BERKELEY, Crypt. Bot. p. 256. BAIL, Sclerotium und Typhula (Hedwigia I, 93). v. CESATI, Note sur la véritable nat. des Sclerotium (Bot. Ztg. 1853, p. 73). COEMANS, Rech, sur la genése et les métamorphoses de la Peziza Sclerotiorum (Lib. Bull. Aead. Belg. sér. 2, IX, Nr. 1). WESTENDOR?P in Lib. Bull. Acad. Belg. VII, p. 80. MUNTER in Lib. Bull. Acad. Belg. XI, Nr. 2. FUCKEL in Bot. Ztg. 1861 ;—Id. Enumeratio Fungor. Nassoviae I (1861), p. 100. (Typhula, lapsu calami Claviceps Euphorbiae.) KUHN in Mittheil. d. Landw. Instituts, Halle I, 1838. HOFFMANN, Icon. anal. Fungor. Heft 3. E. REHM, Peziza ciborioides (Diss. Gottingen, 1872). W. TICHOMIROFF, Peziza Kauffmanniana (Bull. Soc. Nat. de Moscou, 1868, p. 294, Tables 1-4). : ERIKSON, in Kongl. Landsbr. Akad. Handl. Tidskr. 1879 (Typhula graminum), 1880 (Peziza ciborioides). BREFELD, Bot. Unters. ii. Schimmelpilze III (Coprinus), IV (Peziza, Typhula). SCHROTER, Weisse.Heidelbeeren (Peziza baccarum) (Hedwigia, 1879). EIDAM, Botrytis-Sclerotien (Ber. d. Schles. Ges. Nov. 1877). CATTANEO, Sulla Sclerotium Oryzae (Arch. del Laborat. Crittog. di Pavia, 1877). SCHROTER in Cohn’s Beitr. Bd. II (Tulostoma). . E. C. HANSEN, Fungi fimicoli Danici (Vedensk. Meddelelser af naturhist. Forening. Kjobnhavn, 1876); GASPARRINI, Ricerche sulla natura della pietra fungaja e sul fungo che vi sopran- nasce, Napoli, 1841. On the same subject: Treviranus in Vers. d. Naturforsch. in Bremen ;—Id. in Flora, 1845, 17.—Berkeley, Crypt. Bot. 288.—Tulasne, Z. c. Mylitta and allied forms :— OKEN in Isis, 1825. LEVEILLE in Ann. d. sc. nat. sér. 2, XX, p. 247: TULASNE, Fungi hypog. 197 ;—Id. in Sel. Fung. Carp. /. ¢. CorRDA, Icon. fung. VI, t. IX, 39. BERKELEY, Crypt. Bot. 254, 288 in Gardener’s Chron. 1848; p. 829. BERKELEY, CURREY, HANBURY in Proceedings of Linn. Soc. London, III (1858), 102, and Trans. Linn. Soc. Lond. XXIII, 91, t. IX, X. H. GorRE, Tuckahoe or Indian Bread, in Annual Report of Board of Regents of Smithsonian Instit. for 1881, Washington, 1883, p. 687. ~ Rosellinia quercina :— R. HARTIG in Unters. a. d. Forstbot. Instit. z. Miinchen I (1880). CHAPTER II,—DIFFERENTIATION OF THE THALLUS,—-SPOROPHORES. 45 3. SPOROPHORES. ‘Srction X. The sporophores* (Fruchttrager) are branches of the thallus of peculiar form which spring from the mycelium and produce and bear the organs of réproduction. The term organs of reproduction designates the germs of new in- dividuals; by individual we understand the zon as Hiackel uses the word, and the mother-cells which immediately produce them. These organs are distinguished according to the particular case by different names, spores, gonidia, basidia, asci, &c., and the structures that bear them may have corresponding names, as gonidio- phores, &c. Asa Fungus may have more than one kind of organ of reproduction, as will be shown in the sequel, more than one of the special forms just named may appear on the same species. It has been already intimated that the sporophores have been compared with the flowers or inflorescences of phanerogams, because their development usually closes, as in the phanerogams, with the formation of a number of organs of reproduction, by which their growth is limited either absolutely or for a time. This limited growth is accompanied by a form and structure more sharply and characteristically differen- tiated than that of most mycelia, and in many cases by a comparatively large develop- ment. The sporophores therefore are not only the most characteristically constructed part of the plant, but also the most striking on account of their form and size; hence they used often to be taken for the whole plant, and are also at the present time the chief subject of description in botanical works. It follows from what has now been said, that we have to distinguish in the sporophore generally between the points of origin of the organs of reproduction them- selves and the other parts of the structure which may serve them as supports or envelopes or the like, and which in each case bear some conventional name. These parts are almost always raised above the substratum, and are firmly attached to it and fed from it through the mycelium. The mycelium sometimes, not always, has filiform or hair-like organs of attachment, rhzzo‘ds, in the shape of branches of the hyphae which spring from the base of the sporophore and complete the provision for its secure attachment and for the supply of nourishment, at least of that part of it which it obtains from water. They have received the name of secondary mycelium from their resemblance to: the primary mycelium. It has not been ascertained in any in- stance, whether under favourable conditions they are capable of assuming the normal characters of a mycelium and producing sporophores; in many Fungi, for example, 1 [Compounds of the Greek word xapmdés and such terms as ‘fruit’ and ‘ fructification’ are better used only for structures which have some direct connection with the sexual act; hence the term ‘ carpophore,’ the more exact translation of the German Fruchttrager, as well as the terms ‘fruit’ and ‘ fructification,’ which under this limitation would not convey the sense of Fruchttrager in this place, have been avoided and the more comprehensive expression ‘sporophore’ is introduced here as its rendering. Berkeley's specific use of ‘sporophore’ for what Léveillé had , termed ‘basidium’ is no obstacle to the use of the word in the sense here indicated, as the term ‘ basidium’ is now a generally accepted one. The more recent application of the word ‘sporophore’ to designate that stage in the life-history of a plant which is the product of an ovum and which as a whole or in part is concerned with the formation of spores need be no objection to its use here; the terms ‘ sporocarp’ and ‘ sporophyte’ sufficiently denote different casés of that spore-producing stage (see section XXXIII).] 46 DIVISION I.—GENERAL MORPHOLOGY, species of Coprinus, Claviceps, Mucor stolonifer, and Syncephalis, this power does not exist. Sporophores may be divided, according to- their structure, into two groups : simple or filamentous sporophores (Fruchthyphen, Fruchtfaden), consisting of a single hypha or of a branch of a hypha, and compound sporophores (Fruchtkérper) in the sense assigned to the expression ‘compound’ in section I. 1. SIMPLE SPOROPHORES. Section XI. Simple sporophores are branches of mycelial hyphae which » usually rise erect from them, and are themselves branched in a variety of modes characteristic of the different species. When the hypha or its branch has grown to a length which has a fixed average in each species, seldom, as for example in the larger Mucorineae and Saprolegnieae, exceeding a few millimetres, the organs of reproduction, spore-mother-cells, spores, are produced at their extremities in forms which also vary in the different species and groups of species. With the formation of these organs the growth of the sporophore ceases in most cases at once and for ever, as for instance in the sporangiophores of Mucor and in the gonidiophores of Peronospora (section XXXVII). In other cases, such as that of the successive abjunction of spores which will be described in section XVI, the growth, that is the increase in size of the sporophore, comes virtually to an end with the commencement of abjunction; but abjunction may continue at the same spots for a considerable length of time if sufficient nourishment is supplied. The gonidiophores of Penicillium, Eurotium, and Asper- gillus are examples of this kind (see section XVI). In a third series of cases the first terminal formation of spores takes place at the extremity of the sporophore after its apical growth has ceased, and when this formation is completed a fresh growth in length of the sporophore begins at or close beneath it, and is soon stopped by a new formation of spores similar to the first one ; and on one hypha or branch the same process may be again and again repeated. The second case is described, as was said above, in greater detail in section XVI. The first and the third may be illustrated by some examples in the present place, though their consideration will also be resumed in later sections. The thick tubular aseptate simple sporophores of the different species of Sapro- legnia abjoint their extremity, which is club-shaped and filled with protoplasm, by a transverse septum to form a spore-mother-cell (sporangium), in which numerous spores are formed by division of its protoplasm (section XVIII). The spores escape when ripe by an opening at the apex of the sporangium, which elsewhere remains entire. This is all that happens in weakly specimens, which therefore represent our first case. In strong specimens on the other hand which have been duly fed, the transverse septum beneath the empty sporangium becomes convex outwards and projects into the sporangium, and assumes the character of a new tubular point, which grows on into the empty sporangium and often through the opening at its apex into the free space beyond, and finally transforms its terminal portion into a new sporangium. This process may be repeated several times on the same sporangiophore, so that several successive sporangia are nested within one another. The allied genus Achlya differs partly from Saprolegnia in developing one or two opposite lateral branches close beneath the empty sporangium, which themselves CHAP. II.—DIFFERENTIATION OF THE THALLUS.-—SI MPLE SPOROPHORES. 47 put out branches bearing new sporangia. There is here therefore a cymose branching of the sporangiophores. The gonidiophores in Peronospora, which are also without transverse septation, are repeatedly forked or monopodially paniculate. The branches are all at first narrowly conical, and when their longitudinal growth is completed their terminal portions swell into an ovoid form, as is seen in Fig. 20a, and are abjointed to form gonidia, and with this the de- velopment of a gonidiophore of Peronospora comes to an end. But in the nearly allied genus Phytophthora after the abjunction of each goni- dium the narrow end of the branch which bore it swells slightly immediately beneath it, and elongating at the same a time pushes the gonidium so much to one side that it pre- 4 sently forms a right angle with the pedicel. Then in P. infestans the gonidiophore swells at the point of attach- —_FiG.20. Phytophthora infestans, extremity of two simple sporophores. @ forma? e 3° < tion of the first gonidia on the tip of each branch, 4two ripe gonidia on each branch, ment of the gonidium IntO a __ with the beginning of the formation of a third. Magn. about 200 times. small narrowly flask-shaped vesicle, and its upper end elongates at the same time and again assumes the character of a gonidia-forming point. After a time a gonidium is formed on it in the manner described above, and the process is repeated usually three or four times on the same gonidiophore, or as many as twelve or fourteen times in luxuriant plants. Older simple gonodiophores therefore, when examined dry, are seen to bear a number of lateral nearly equidistant ; OY gonidia forming a right-angle with the gonidiophore, and each standing on a flask-shaped swelling (Fig. 204). As the ripe gonidia fall off instantly in water, preparations treated with water have the older branches of the gonidiophore swollen at inter- 7 vals into the shape of a flask with a single unripe gonidium at most at its apex. a Z é The simple sporophores of Haplotrichum, Gonatobotrys, and Arthrobotrys (Fig. 21) are . short erect rows of cylindrical cells usually simple, but sometimes with single branches. The apex of the uppermost cell swells up considerably in Haplo- trichum, slightly in the other species, and puts out numerous crowded protuberances, which together Aer form a small spherical head and develope into ee gonidia. This is the whole of the development in ; : . F Haplotrichum. But in the other two forms the pie ieee acalealben he day spo ras apex of the gonidiophore begins to lengthen again 7, With the frst head of gonidia. ? second head . above the first. cold sporophore with the trace after the first head is matured and grows through °° five successive heads. After Fresenius (Beitr). Pi 3 a@ and c magn. about 200 times, 6 less highly mag- it, and thus the head becomes a whorl surrounding __ nifiea. the flanks of the gonidiophore; the growing end of the gonidiophore attains to about the length of one of its lower segments, be- comes septate above the first head and then forms a new head at its extremity like the first. This proceeding may be repeated several times, till the gonidiophore is at iS v 48 DIVISION I,—-GENERAL MORPHOLOGY. length occupied by several whorls of spores at a cell-length’s distance from one another, or shows their points of attachment when the spores themselves have dropped’. The gonidiophores of Sclerotinia Fuckeliana, known by the name of Botrytis cinerea, send out several lateral branches in a paniculate manner beneath their apex, the lower of which are themselves branched. The somewhat. enlarged and rounded ends of the primary hyphae and of its branches abjoint many spores simultaneously on their surface. As these ripen the sporiferous terminal cells of the hypha as well the entire lateral branches die, dry up, and almost disappear, while the spores are clustered together without arrangement. But a new growth begins in the cell beneath the terminal cell ; it either simply elongates, and then forms a new sporiferous structure, or it sends out one or more strong lateral branches which behave in the same way as the primary hypha. Formation of sporiferous structures and prolification may take place repeatedly on the same hypha; traces of the branches that have been cast off are seen in the circular scars which project a little towards the outside*, 2. COMPOUND SPOROPHORES. Section XII. The chief forms of the compound sporophores of the Fungi are well-known to every one; the stalked umbrella-like and the sessile flabelliform or horse-shoe-shaped pz/eus of the Hymenomycetes (Champignon, Mushroom, Amadou- fungus), the club-shaped or shrubby Clavarieae, the perzdia of the Bovistae and Truffles, the cups of Peziza, and lastly the simpler forms which issue as flat or pulvinate bodies from the surface of dead or living plants and are comnpeed under the terms /ayer, stromata, or receptacula. Some of the last more simple forms may be regarded as transitions to simple sporophores, being indeed aggregates of these and exhibiting a more or less compact and characteristic union, which may however vary in one and the same species. Such are the gonidial layers of Cystopus and Hypochnus centrifugus, Tul. The gonidiophores of Penicillium are sometimes single hyphae, sometimes are united together into tufts ' to which Link gave the name of Coremium; and the same is the case with the gonidiophores of the insect-killing Sphaeriaceae, in which the club-shaped branching tufts, which are often of considerable size, are known by the name of Isaria*. But by far the largest number of compound sporophores, and it is with these that we are chiefly concerned here, show much more constant and more distinct differentiations. Amid the great diversity of individual peculiarities one character may be regarded as almost universal, namely, that a compound sporophore produces its characteristic organs of reproduction (spore-mother-cells) in large quantities, and that they are grouped in a definite manner and at definite spots upon it. The spore-mother-cells form there continuous strata or aggregates of some other shape, either by themselves or accompanied by accessory organs usually termed paraphyses. These aggregates are conveniently included under the general name of 1 Fresenius, Beitr. t. III, V.—Corda, Prachtflora——Coemans, Spicilége, No. 8.—Woronin, Beitr. ITI, t. VI. ? Fresenius, Beitr. t. II. ' $ Bot. Ztg. 1867, 1. CHAP, II,—DIFFERENTIATION OF THALLUS. —COMPOUND SPOROPHORES. 49 hymenium or sporogenous layer, and are thus distifguished from the rest of the sporophore. At the same time descriptive mycology, following convenience and tradition, is in the habit of employing special appellations for the hymenia of the several orders and reserving the word: hymenium for the Hymenomycetes. The structure of the hymenia will be described in later chapters. Many points also in the structures and especially in the development of the sporophores, in the narrower sense of the word, must be reserved for future consideration, partly because a comparative examination of their first inception presupposes a previous discussion of sexual relationships, partly because we have frequently to deal with facts which are characteristic of single divisions, and which it will be more convenient to discuss when we are engaged with these in Division I]. Meanwhile it may be well to notice here a few phenomena of very general occurrence. It is only in certain cases that a compound sporophore begins as a terminal or intercalary portion of a single hypha, which portion then developes into its ultimate form by successive cell-divisions in every direction and by further differ- entiations and growth in definite directions, somewhat after the manner of the anther of a Phanerogam, if such a comparison is admissible. Some fycnzdia among the Pyrenomycetes (see Division IT) show this exceptional behaviour. The general rule here, as in the development of sclerotia and mycelial strands, is that the sporophore proceeds from the union of branches of the hyphae, and grows by the elongation and branching of these according to a general plan and in directions determined by the species, and that new hyphal branches are introduced between those previously formed in agreement with the original design. ‘This earliest stage, which may be called the meristematic stage, and in which new segments and new hyphal branches are added, is succeeded in every section of the sporophore by a stage of increase of volume of the existing elements and of their permanent differentia- tion, the amount of which is very different in different cases, and reaches its highest point in the Gastromycetes and especially in the Phalloideae. The hyphal branches which form the compound sporophore originate in some cases in a single branch of the mycelium, which may have the morphological significance of an archicarp or homologue of a female sexual organ with its immediate supporting structure, as in Eurotium, or have no sexual relationship, as was pointed out above in the sclerotia of Coprinus and Typhula variabilis, and in the sporophores of some species of Coprinus which were shown by Brefeld especially to be produced without the intervention of sclerotia. In the majority of better-known cases the formation of the compound sporophores begins with the union of two or several or many hyphal branches of different origin. This is the case with some of the sporocarps of the Ascomycetes which will be described at length in Division II, with the very simple hymeniophore of Exoascus Pruni, with _ most of the compound sporophores mentioned above as growing from sclerotia (the various species of Peziza, Claviceps, Typhula gyrans, &c.), and the compound sporo- phores of Agaricus melleus whichhave their origin, according to Hartig’, in the mycelial strands in the same way as the ordinary mycelial branches. Most of the Hymeno- mycetes which are not fleshy might be added to the list, inasmuch as their compound * 1. c. above, p. 28. [4] E 50 DIVISION I.—GENERAL MORPHOLOGY. sporophores, as far as they have been observed’, always begin their development as comparatively large compact tufts of hyphae springing from the mycelium, and we may even venture to assume that the great majority of compound sporophores take their origin, as here described, from many hyphae. At the same time it must be acknowledged that it has been found possible to follow them back to their very first beginning with perfect certainty only in the few cases which have been noticed above. ES Many inconspicuous compound sporophores, such as the gonidiophores of Uredi- neae and the stromata of many small Pyrenomycetes, remain as it were in the stage of the tufts of hyphae and pass into their ultimate form without further remarkable phe- nomena of growth. But where a larger structure is produced, the course of development, amid great variety of detail, discloses two chief types, which closely resemble the two types of growth above described, for the mycelial strands on the one hand and for the sclerotia on the other. In the one type, as in the formation of sclerotia, the growth is nearly unzform for a long time in all parts of the structure; then comes the second chief stage, the ultimate development by internal differentiation. The compound sporophores of the Gastromycetes show this mode of proceeding in the most marked manner. In the other type the general course is progressive®, just as it is in the mycelial strands or in the single hyphae, advancing in the direction of fixed spots in the surface, which are themselves pioneers in the advancing growth and maintain it by formation of new cells ; as any section becomes removed from these spots growth in it ceases, and its component elements assume their definitive character. According to the form of the whole structure and of the superficial portion of it in which progressive growth occurs, this growth may be said to advance towards the apex, to be apical (acropetal), or to be marginal, and the peripheral progressively growing spots by another usage may be termed growing points or margins ; or growth is progressive towards the whole of the free surface of the structure which bears the hymenium, as in the horse-shoe-shaped pilei of Polypori which are several years old, and in other Hymenomycetes also with various modifications and limitations. Growth thus on the whole progressive does not preclude intercalary areas of new formation and extension from making their appearance between portions in which these processes had ceased; but the actual occurrence of these areas has never been distinctly proved in any of the cases which belong strictly to this type. On the other hand, the combination of the two types of growth has been ascertained in a considerable number of species. We find, for instance, internal differentiation and subsequent progressive growth in the compound sporophore which is the chief product of Amanita. The young stipe of the Coprineae*® has a transverse intercalary zone in the part just below the apex, in which there is continued formation of new cells by (meristematic) division; the velum also has intercalary growth, but all the growth of the pileus and the final elongation of the stipe is progressive. In the Xylarieae, Cordyceps, &c. the growth of the club-shaped sporophore is progressive 1 Hartig, Zersetzungserscheinungen d. Holzes, p. 21 (Polyporus annosus), p. 32 (Trametes Pini), p. 41 (Polyporus fulvus), p. 50 (P. mollis), p. 98 (Hydnum diversidens), &c. 2 Goebel in Arbeiten d. Bot. Instit. zu Wiirzburg, IT, 354. ’ Brefeld, Schimmelpilze, III. CHAP, IJ.— DIFFERENTIATION OF THALLUS.—COMPOUND SPOROPHORES. 51 (acropetal), and the perithecia are subsequently formed in them by internal differentia- tion; other instances might be given. Some compound sporophores with acropetal growth are normally and often uniformly branched, as in many Clavarieae, the Xylarieae, and Thamnomyces. The ramifications appear always to arise as bifurcations of the growing points, but this has not yet been sufficiently investigated. Inquiry is also needed in the cases of supposed monopodial and always slightly irregular branching seen in Agaricus racemosus, Isaria brachiata, and some others. Peziza Sclerotiorum often has irregulary disposed exogenous branches on the stalk-like portion of a compound sporophore, especially on the part near the ground. We are not concerned here with branching which is purely adventitious, artificially excited, or monstrous. The duration of growth under normal and favourable conditions differs much in different species. In the small delicate fleshy Coprini the whole process, from the commencement to full ripeness and decay, may be completed, according to Brefeld, in 8-10 days, while the solid woody Polyporeae maintain a progressive growth for years; Trametes Pini, for example, according to Hartig for 50-60 years. There are all possible intermediate cases between the two extremes. Long-lived ‘species necessarily advance and remain stationary periodically with the change of the seasons. Apart from this latter influence, the course of growth under uniformly favourable conditions is marked by the same order in the Fungi as in the higher plants. First there is the laying down of new parts by formation through division of meristem of new tissue-elements accompanied by a small increase in volume ; then the differentiation of the tissues takes place, and lastly the final elongation and increase of volume. The first two operations are performed slowly and steadily at least relatively to the third, the one passes gradually into the other; and the transition to the third stage is also gradual in the forms which are not fleshy, such as the Xylarieae and the leathery and woody Hymenomycetes. But in the forms with fleshy succulent substance, especially the Hymenomycetes and Phalloideae, the transition to the third stage is often abrupt, and this stage itself is traversed with relative and absolute rapidity. Of the 8—1o days occupied by the growth of the small Coprineae mentioned-above the last tenth at most was devoted to the final elongation and expansion, the former stages requiring 7-9 of the 8-10 days. In the case of many other fleshy Hymenomycetes, such as Amanita, the time necessary for the first two stages is much longer than this, and Schaffer is not much beyond the mark in estimating it at a year in Phallus impudicus’ ; but more exact-determinations are desirable, But the final elongation and expansion are accomplished in all these cases, under favourable circumstances, in a few days at most. The proverbial rapidity with which the succulent Fungi shoot up from the ground, as is the case with the green vegetation in spring, is chiefly due to the abruptness of the final extension of the structure which has Jong been in existence and slowly and gradually developed. ! It has in no case been shown with perfect certainty that the peripheral extremities of the hyphae, which take the lead in progressive growth, remain the same during the whole process, and that the compound sporophore therefore is built up of the united branches of a constant number of monopodially branched primary ! Der Gichtschwamm mit dem griinschleimigen Hute, Regensburg, 1760, p. 7. E 2 > 52 DIVISION I,—GENERAL MORPHOLOGY. hyphae destined from the first for the particular structure. In small compound sporophores with an apex which continues narrow, being composed of only a few hyphae, like those of Typhula to be noticed presently, it may, though it need not necessarily, be assumed that such is the case. In the much more frequent cases in which the advancing apex or margin becomes constantly broader with uniform thickness and separation of its elements, new hyphal branches must be introduced one after another between the original ones, or take the place of them in sympodial succession. In long-lived species with periodical cessation of growth in the cold or dry season most of the extremities of the branches must die away, and be replaced when growth begins again by branches of deeper origin which thrust themselves between them. The position of the dead extremities or the portions of new growth limited by them may then be seen as zones in the older structure. The consideration of special phenomena of development is deferred to a later page for the reasons assigned above. But it will be well to give a more detailed description in this place of some examples at least of progressively growing compound sporophores, because this mode of growth is very general both in the different divisions of the Fungi and in sporophores of very different morphological value. The examples are for the most part those of the first edition of this book. 1. The stalk-like compound sporophores of Typhulae which form sclerotia, Typhula variabilis especially, begin on the sclerotium as the bundle of firmly united parallel hyphae with their extremities curving dome-like towards each other, which was noticed above on page 38. » The compound sporophore increases in length. The united extremities of the hyphae in the dome-shaped apex continue all the while very delicate and full of protoplasm, and comparatively small-celled. As the segments of the hyphae are further removed from the apex of the growing sporophore they increase steadily over a certain distance in length, breadth, and thickness, and the whole structure increases in compactness and firmness ; no further augmentation takes place at its base. From these facts it appears that the growth in iength of the sporophore, so far as it depends on formation of new cells, takes place at and close beneath the apex by the apical growth of the united hyphae ; this is therefore the growing point. Then the cells produced at the growing point elongate in the order in which they are formed and assume their ultimate form. As the elongation commences the primordia of scattered unicellular hairs make their appearance as branches on the superficial hyphae of the lower sterile portion, and on the upper part the dense weft of the hymenial layer. At length the activity of the growing point ceases and with it the growth of the whole sporophore. In the interior of the parts more remote from the growing point there appears to be no further formation, or at any rate no considerable formation of new cells, either by division of previously formed cells or by addition of new hyphal branches introduced between those already in existence’. 2. The compound sporophores of Selerotinia Sclerotiorum (Fig. 22), the early stages and special structure of which will be again described in Division II, burst forth as cylindrical bodies from the sclerotium, grow in this form to a length of 1o mm. more or less, and then increase in breadth at the apex in such a manner as to pass through the shape of a club into that of a stalked funnel-shaped cup, which may finally have its margin turned outwards. The young cylinder consists chiefly of a bundle of nearly parallel hyphae; the slender delicate-walled extremities of the hyphae 1 See also Brefeld, Schimmelpilze, III.—Reinke u. Berthold, Die Zersetzung d. Kartoffel durch Pilze, p. 58. - CHAP, II.--DIFFERENTIATION OF THALLUS.-—COMPOUND SPOROPHORES, 53 are in the apex of the structure and form its growing point, in which growth in length continues, while it dies out in the parts below it as these become successively further removed from it and the cells of the hyphae have grown longer and thicker. The parallel arrangement of the hyphae is not everywhere maintained ; firstly, a number of short hyphal branches bend round obliquely upwards and outwards close below the apex, and terminate in the free lateral surface, where they form a cortical layer to the compound sporophore; and secondly, in the first stages of the develop- ment, when the sporophore is scarcely visible to the naked eye, the hyphae surrounding. the longitudinal axis are somewhat more loosely united together than in the periphery and have their extremi- ties slightly curved towards the axis. In this state the primordial sporophore grows to a certain length by continued apical growth in a straight line. Then the growth in length of the axile hyphae is retarded while that of the peripheral hyphae advances rapidly. In this way a narrow canal, which can only be seen under the microscope, is formed in the apex of the cylindrical sporophore with its upper margin bounded by the slightly incurved extremities of the hyphae. And while growth constantly proceeds in the direc- tion of this margin, successive formations of new and jag, we Pestea (Sclerotinia, Fuckel) similar elements take place in it, and behind it in- = Sevsttorum, Lib. Sclerotium with emerg- ee p ing sporophores of different ages. Nat. tercalary additions (which however gradually cease size. to appear), together with the first formation and development of the hymenium and other parts: thus the cylindrical body gradually assumes the form of the stalked funnel. The final growth in thickness of the stipe, which is however only slight, occurs chiefly in the periphery, and as the axile hyphae share but little in it, a narrow canal is formed which traverses its length. In other species of stalked Peziza, P. nivea for instance, I have not myself observed the first stages in the formation of the cups; they are not however difficult of obser- vation, and several accounts have been given of the way in which they grow for a time by formation of new elements in their originally involute margin, and at length assume their final form by an expansion of their tissue- elements advancing in the direction. of the margin. 3. The sporophore of Stereum hirsutum (Fig. 23), which is de- scribed as a pileus divided in half without a stalk and laterally at- tached, is generally an irregularly roundish flat disk, the larger part 54, 25 sterewm nirsutum, Fr. Vertical radial séction through the of which stands out at right angles —_ margin of a fresh pileus slightly magnified and giving a partly diagram- ° matic representation of the course of the hyphae; ~ the advancing from the substratum, while the other margin with two zones behind it, # the hymenial layer, 7 medulla, and often very small part is firmly —” "™* * “vering of hairs. fastened to it; if the substratum is vertical, the projecting part of the Fungus has a horizontal direction, its upper surface is thickly covered with hairs, and on its under surface is the hymenium. We need not here take notice of other and more irregular forms which are of frequent occurrence. The sporophores first appear in the form of semicircular gray tufts of hyphae 1-2 mm, in breadth. These are formed on stout mycelial filaments which spread in large numbers through the dead wood inhabited by the Fungus. The tufts are formed of numerous hyphae, which spread from a central point with tolerable regularity . 54 DIVISION I.—GENERAL MORPHOLOGY. like the spokes of a wheel. They are closely interwoven at the centre, but separated towards the circumference by constantly increasing interspaces, and thus the surface is covered with spreading hairs. These appear under the microscope to be colourless or of a uniform brownish colour, while the hyphae of the central tissue is coloured by granules of a reddish-yellow pigment. As the development proceeds the lower half of the hemispherical body, lower that is in relation to the substratum which is supposed to be vertical, takes a reddish-yellow tint and its surface becomes smooth and velvety. Thin radial sections following the direction of the hyphae show that, as far as the last-mentioned character extends, numerous hyphae, most of which contain reddish-yellow pigment-granules, have grown from the central weft to the surface and have thrust themselves in large numbers everywhere between the previously formed hairs and enclosed them. The upper half of the hemispherical compound sporophore retains its original character. Now begins a vigorous longi- tudinal and apical growth of the hyphae which run into the margin of the reddish- yellow under surface of the young pileus, while those which terminate in its middle portions elongate but little or not at all. Hence the upper surface becomes concave and the horizontal portion of the pileus raises itself from the substratum, while the growth of the hyphae advances at its margin. Sections show that the margin consists of a massive and compact layer of truncated rather thick hyphal extremities, which incline slightly towards the under surface and usually contain reddish-yellow pigment-granules. These extremities join on to the perfect hyphae of the pileus close to the point of origin of the latter ; these perfect hyphae being distinguished from them by their pellucid contents, but not by greater thickness, and running in radiating lines parallel to the surface of the pileus. The differentiation of the tissue of the pileus begins close behind the advancing margin, and results in a lower colourless medullary stratum, and an upper thin rind-stratum distinguished by membranes of a clear brown colour. Numerous hairs begin to be developed on the upper surface - nearer the margin, and the hymenium on the lower surface. The former are simple stout hyphal branches which either spread or are curved backwards; the outermost of them project beyond and mostly cover the growing margin. Numerous branches run obliquely and with a slight curve close behind the margin towards the hymenial surface. The nearer the base of the pileus, the more numerous are the hymenial elements which are introduced between those previously formed, and the more decidedly do they assume the vertical position as regards the surface of the original constituents of the hymenium. The portion of the pileus which is attached to the substratum shows essentially the same mode of growth as that which projects from it, only the hairs on its outer surface penetrate as rhizoids into the substratum. Measurements by J. Schmitz and microscopic examination show that the enlargement of the pileus takes place only next the margin’. ; 4. The unveiled umbrella-shaped pileus with central stalk of the Agarici (Fig. 24) appears at first on the mycelium as a small cylindrical, ovoid, or even spherical body, pointed at the upper end and consisting throughout of very delicate firmly united hyphae running longitudinally. At a very early stage, when the entire structure in the specimens which I have examined is 3-2 mm. in length, the extremities of the hyphae at the upper end spread in every direction as they grow and at the same time branch copiously. This gives rise to a small hemispherical head separated from the lower portion by a shallow annular furrow, the primordium of the pileus (Fig. 24a). A vigorous growth then commences in the extremities of the hyphae which form its margin, and they constantly elongate, but at the same time retain their original thickness, and continue as closely woven together as at first ; there must therefore be a constant introduction of new branches between the earlier ones in the direction of the surface of the pileus. The hyphae which run towards ? See also R. Hartig, Zersetzungserscheinungen d. Holzes, p- 130, t. XVIII. CHAP. 1I.—DIFFERENTIA TION OF THALLUS.—COMPOUND SPOROPHORES. 55 the apex of the pileus soon cease to lengthen; they become the tissue of the middle of the pileus, while as the margin advances the hyphae which run into it send out numerous straight or curved branches upwards and outwards, which in their turn soon cease to elongate and form the general tissue of the pileus (Fig. 24 4). Closely crowded branches from the under surface of the layer which runs into the margin grow at the same time and in the same centrifugal succession from a curved base perpendicular to the under surface of the pilets; these are the beginnings of the tissue that bears the hymenium and of the hymenium itself. They are at first of uniform length, and the surface of the hymenium is smooth at first, as Hoffmann rightly affirms in opposition to a former incorrect statement of mine, though it only continues so for a short time. The elongation of the hymenial hyphae which grow vertically downwards takes place in alternating radial bands in varying degree. In some it continues longer, and they project beyond the smooth surface as the trama of the lamellae, on which the hymenial elements arise in the position already described, advancing from the base toward the free edge. The hyphal extremities cease to elongate at an earlier period in the intervals between the lamellae, and RECORIC directly elements of the hymenium. : During this growth by terminal and marginal formation of new constituents, the parts at a distance from the growing point or mar- gin enlarge by expansion of their cells, and the tis- sue which is at first uni- form is differentiated at the same time into the several layers of the ma- ture sporophore. It is readily observed that this process of expansion also advances in the stipe from below upwards, and in the pileus from the centre to the margin. To this ex- pansion of the originally FIG. 24. Agaricus (Collybia) dryophitus, Bull. Radial longitudinal section showing the course of the hyphae. @ a quite young and entire specimen 1°3 mm. in height; first very small elements to beginnings of the pileus. & older specimen with the pileus 2°5 mm. in breadth; 7 piece several times their former _°f @ lamella. Slightly magnified. size is due in great part, especially in rapidly growing fleshy sporophores, that enlargement which may be seen with the naked eye. In Agaricus (Mycena) vulgaris for instance I succeeded in deter- mining, by measurement of the cells and counting their number on the transverse section, that the increase in length and breadth of the stipe, which becomes on an average 50-60 mm. long, from the time when its length was about 3 mm. and its cells could be exactly measured, must be almost exclusively. due to extension of the cells. I obtained the same result in the case of Nyctalis parasitica ; the conclusion was similar in the case of Agaricus (Collybia) dryophilus, Bull., but less precise on account of the very unequal length of cells placed at the same height. Exact measurements can scarcely be made in the pileus owing to the curvatures and want of uniformity in the cells, but here too it is evident that there is an expansion of the tissue-elements, which often exerts considerable force and advances towards the margin. It appears to me to be doubtful whether there is also any formation of new cells by transverse division of the primary cells of the hyphae and by pro- duction of new branches in parts removed from the margin. It does not take place in either of the two cases just mentioned, but they are too isolated to allow of our drawing a general conclusion from them. Branches often occur on hyphae which 6 DIVISION I.—GENERAL MORPHOLOGY. are much expanded or are in the act of expanding, which are little if at all thicker than the primary hyphae and are rich in protoplasm, and therefore look as though they were of recent formation. Whether they are really new branches, or only branches formed at an early period but not sharing in the expansion, must remain undecided. In the hymenium certainly new elements are introduced between the earlier ones usually for some time after its first formation. A distinct efinasty prevails at first in the general growth of the pileus; the parts belonging to the upper side grow more vigorously than those of the lower, and according to the position and breadth of the annular zone which is most strongly epinastic, either the margin of the pileus is rolled inwards or the whole of the under or hymenial surface approaches or even touches the stipe; or both effects are produced, and this is most frequently the case. Subsequently, when growth is coming to an end, the epinasty changes to Ayfonasty, the under side grows more strongly than the upper, and the entire pileus expands with more or less rapidity in each separate case from its original bell-like or conical form into that of an umbrella, while the incurved margin may even become curved upwards and outwards. We cannot enter here into the variations which occur in the development and form of the pileus in the several groups and species, and indeed we possess a very limited number of exact observations on them. The account which has just been given is founded on my own examination of Agaricus (Mycena) vulgaris, Pers., A. (Collybia) dryophilus, Bull., and Nyctalis parasitica, Fr., on the study of the history of development of Agaricus (Clytocybe) cyathiformis and Cantharellus infundibuli- formis in conjunction with Woronin, and on the works of H. Hoffmann. Hoffmann indeed makes the hyphae of the middle of the pileus in the section Mycena not run radially towards the surface and there terminate, but parallel to the surface of the pileus (for so I understand his expression ‘ horizontal’); and in this small point our otherwise conformable accounts differ. It is possible that different species vary in this respect. The course of the hyphae can be readily seen to be as I have stated it in Agaricus vulgaris, when the pileus is still young, but not in the older states ; then the whole of the superficial tissue of the pileus assumes the character of a tough gelatinous felt, which may be removed as a coherent membrane from the pileus,-and in which the hyphae have no particular arrangement. In most of the sporophores of which we are here speaking, especially those of a fleshy consistence, growth proceeds without interruption and soon reaches its ter- mination ; it may go on more slowly or be arrested for a time, if the conditions are unfavourable, and afterwards recommence ; more serious injuries, especially persistent drought and cold, stop it altogether. The power of withstanding such unfavourable influences varies much in the different species. On the other hand, as has been already stated, the pileus in many leathery and woody forms, such as the Xylarieae and especially the Hymenomycetes, has the power of recommencing suspended growth with the return of favourable conditions. During each stationary period in the Hymenomycetes the hyphal extremities in the margin and upper surface of the sporophore, which for the most part die off, assume in many cases another colour and usually a darker one than that of the rest of the tissue, which is seen therefore in sections to be divided by dark lines into the zones already mentioned (Fig. 23). The tissue of the sterile surface also has often a different colour at the beginning from that which it has at the end of a period of growth ; and at-the commencement of the period of growth it often swells suddenly into a cushion, which runs quite round the margin of the pileus and flattens out again towards the margin with the continuation of growth. The periods of rest and growth are thus here as elsewhere indicated on the sterile surface of the Fungus, as in somé other plants, by zones concentric with the margin of the pileus, and usually answer exactly to the interior zones but are sometimes less distinctly marked. It is scarcely necessary to mention examples of these ‘pilei zonati,’ since they occur in many of the most common and best-known species, CHAP, 11,— DIFFERENTIATION OF THALLUS.--COMPOUND SPOROPHORES. 57 such as Stereum hirsutum, Polyporus zonatus, P. igniarius, P. fomentarius, P. Lenzites and their allies. The hymenial side in most of these Fungi increases in circumference only as the margin of the pileus continually advances, but no increase in thickness is thereby brought about. On the other hand there is an addition to the free hymenial surface in every period of growth in many species of Polyporus, especially in the Fomentarii of Fries, in Polyporus fomentarius for example, P. igniarius and P. Ribis, and in Trametes Pini, Corticium quercinum and allied forms. Sections therefore through older specimens show zones on the hymenial side as well as in the rest of the tissue of the pileus ; each zone answers to a zone in the substance of the pileus and is its con- tinuation, the youngest hymenial zone being continued into the outermost marginal zone of the pileus. Persoon? and Fries? call the zones of these Polypori annual zones. They may no doubt be correctly compared in certain points to the annual rings of Dicotyledons, but it has never been distinctly proved that only one new zone is formed each year in these plants. There is no doubt that many zones are formed in the course of a year in most of the other zoned mushrooms. J. Schmitz has shown this in detail for Stereum hirsutum, and there are a certain number of many-zoned pilei in the Hymenomycetes which only last one year. Section XIII. The structure of the mature compound sporophores either continues to be evidently hyphal, or it becomes pseudo-parenchymatous in the sense of the word explained in section IV. When a compound sporophore is much differentiated both kinds of structure may occur in different regions of it and in different strata. In the first case the course of the ramification of the hyphae may be quite irregular and they may interlace in every direction, as in most sclerotia; this happens in sporophores in which the growth is not peripherally progressive, and in the small structures mentioned on page 51 in which this mode of growth is at least only feebly developed, as in the Uredineae and in endophytic Ascomycetes (Rhytisma, Polystigma, Epichloe). The pileus of Morchella and Helvetia may be mentioned in this connection. But where the growth is distinctly progressive, whether apical or marginal or towards the surface, the great mass of the hyphae usually follow a course corresponding to these directions, and in large compound sporophores the surface of sections or broken pieces may often appear fibrillate even to the naked eye. The course of the hyphae in these cases either corresponds exactly with the form and direction of growth of the parts, as for example in Stereum hirsutum (Fig. 23) and in the stipes of the smaller Agarics, or the hyphae are sinuous and interwoven with a larger or smaller number of ramifications spreading in the most different directions, and forming what at first sight appears to be an entanglement of threads, such as we see for example in the tissue of the pileus of many Agarics. But sections made in the right directions will usually show that here the primary hyphae follow a course which answers to the general rule. There are however some exceptions ; a striking _ instance of the latter kind is found in Polyporus annosus*, which has persistent progressive growth of the margin of the pileus and of the hymenial projections, yet, except in the outermost margin of the latter, the course of the slender interwoven 1 Essbar. Schwamme, p. 17. * Epicris. p. 463. * R, Hartig, Zersetzungserscheinungen d. Holzes, p. 21. 58 DIVISION I.—GENERAL MORPHOLOGY. hyphae and of their ramifications appears to be entirely without arrangement. R. Hartig’s description of Polyporus fulvus should also be consulted *. Compound sporophores with distinct pseudo-parenchymatous structure could only be illustrated by a number of individual cases all differing in many points from one another, but such an enumeration would be out of place here. — One feature common to most, if not all, compound sporophores of all types ot structure is the more or less distinct separation of a peripheral layer from the inner tissue. Compound sporophores with much internal differentiation, among the Gastromycetes especially, exhibit many peculiarities in connection with this point, which will be noticed again in later sections in describing individual cases. ‘The separatior in compound sporophores with progressive growth, and also in some small ones with only slight differentiation, usually consists in the fact that an inner less compact and firm mass, which may be termed the medulla or medullary mass, is surrounded in the parts which do not directly bear the organs of reproduction, as in the sclerotia, by a peripheral rzvd or cortical layer, in special cases termed also the fedlicula or cults, which is the outer boundary of the whole structure. When the compound sporo- phore forms organs of reproduction directly on its surface, the hymenial layer takes the place of the cortical. Both the medulla and the rind may be separated again into subordinate layers. The rind is distinguished from the medulla either by the structure, size, and firmness of union alone of its elements, their arrangement (the fibrillation) being similar in both, or their arrangement also is different. In the first case the rind is usually of a firmer texture than the medulla owing to the less breadth and closer union of its elements. This is its character in very many fleshy or cartilaginous Mushrooms, such as the larger Clavarieae, Calocera, many Agaricineae and Pezizeae, and in the stroma of Rhytisma. The cells of the rind have also not unfrequently coloured sclerosed walls, which are wanting in those of the me- dulla, as for instance in Peziza hemisphaerica, Rhytisma, Stereum hirsutum, &c. In other forms the rind is distinguished from the medulla by gelatinous cell-walls, as in the pileus and stipe of Agaricus (Mycena) vulgaris, in the pileus of Russula integra, in Panus stypticus, and many other Agaricineae, the outer covering of which is a tough gelatinous felt, while the interior tissue is not gelatinous. A different arrangement of the elements of the rind from that of the medulla occurs frequently in compound sporophores with hyphal structure; the hyphae of the medulla follow in their course the form of the sporophore, but numerous curved branches with their convexity towards the apex pass off from its hyphae in the direction of the surface, where they terminate in copious ramifications and close union with one another. The extremities themselves either form a tangled weft, as for instance in Auricularia mesenterica and species of Poly- porus, or else they are placed perpendicularly to the surface, so that the rind appears to be formed of palisade-like cells or cell-rows, as in Peziza Sclerotiorum, in the large- celled tissue of the surface of the stipe of Helvella crispa and H. elastica, in the outer and inner surface of the hollow stipe of H. esculenta and Guepinia contorta?, in the smooth surface of the pileus of Polyporus lucidus (Fig. 25), and-in that of _ P. fomentarius. ' R. Hartig, Zersetzungserscheinungen d. Holzes, p. 40. * Dacryomyces contortus, Rabenh. Herb. Mycol. Nr. 1984. CHAPTER III.—SPORES OF FUNGI. 59 A very large majority of Fungi have spreading Aazrs on their surface, which arise as branches from the hyphae of the compound sporophores and show this origin even where its final structure is pseudo-parenchymatous. Some of them come from the hyphae of the surface itself, some originate at a greater or less depth beneath it and pass obliquely to the outside through the layers of tissue that cover their point of origin. They are simple cells or cell-rows and branched or unbranched, and scarcely yield to the hair-formations or the higher plants in variety of form, direction, size, colour, structure, and thickening of their membranes; the most varied series of these formations is to be found in Peziza and the allied Ascomycetes, and in Erysiphe and Chaetomium. In many cases the hairs are closely combined in tufts, which appear to the naked eye according to the species as bristles, scales, or warts, as for instance on the surface of the pileus of Polyporus hirsutus and P. hispidus, Of tongitadisal secton through the surface Hydnum auriscalpium, Tremellodon gelatinosus, &c., or Mase isstme ese as cylindrical tufts expanding into the shape of a funnel at their extremity, such as are found on the sterile surface of the pileus of Fistulina hepatica, and from their shape were once described as rudiments of the tubuli of the hymenial surface*. Ifthe superficial felting of hair is very thick, it may be a question whether it should not be considered to be a cortical layer, and the determination must rest on what is suitable in each particular case. Where the compound sporophore is very close to the substratum, single hairs or tufts of hairs often assume the character of rhzzozds. Here would naturally be the place to speak of the Lichen-thallus and especially of its fruticose and foliose heteromerous forms; but it will be more convenient to reserve this part of the subject to Division III. DIA HHA \ INDY it i a cS CHAPTER III. Spores oF FUNGI. Srction XIV. The propagation of the Fungi, in the widest sense of that word which implies the production of new bions through a mother-individual, is generally effected by the abjunction, and in most cases by the complete separation, of cells from the maternal structure, which then develope into daughter-bions if the necessary . conditions are present. The single cell thus abjointed from the mother and capable of this development into one or more than one bion we term here a sfore; - empirically we fix that moment and condition of its development, in which abjunction from the mother as its nutrient source is effected, as the moment and condition of its r7pemess or maturity; the commencement of the further develop- ment of the ripe spore is its germination. } Fries, Syst. Mycol. I, 396. 60 DIVISION I.—GENERAL MORPHOLOGY. It is a universal histological law that every spore is the daughter of one or some- times more than one mother-cell, which is consequently called the spore-mother-cell. There are many and great differences between spores and their mother-cells in respect of their special qualities, structure, and mode of formation, and in respect of - their position in the life-history of the species and the homologies which result from it, and several different kinds of spores may be formed in the course of development of a single species. Hence there are several categories, kinds, or forms of spores and spore-mother cells, that may be distinguished according to these different points of view. In their terminology these distinctions are expressed sometimes by adjectives, sometimes by compounds of the word spore, as swarm-spores, ascospores, &c., some- times also by special words, gonzdium, ascus, bastditum, and others. Each of these terms signifies a spore or its mother-cell in the general meaning of the word above indicated, with a definite specific reference. A fuller explanation of the terms and an account of the reasons for their adoption are reserved for Chapter LV. The distinction between spores and their mother-cells on the one hand and vegetative cells on the other is naturally drawn first of all from cases in which the differences are most distinctly marked, and these constitute the large majority. It is to be expected that in a large and much graduated series of forms some would occur in which those differences would be less marked, sometimes indeed be almost obliterated. As examples of this may be mentioned the vegetative form described on page 4 as Sprouting Fungus, in which each sprout may be quite rightly termed a spore in the above acceptation of the word, and in the gemmae formed by the abjunction of cells with the power of germination from the vegetative hyphae in the Mucorini, Tremellineae, and Ascomycetes, which will be subsequently described. No confusion would be caused by a consistent use of the word spore in these cases. Whether it would be convenient that other terms should be introduced in its place is a matter to be determined by judicious agreement in each case. Many of the peculiar characters of spores and many of the phenomena attending their formation and ripening recur in the most different groups of the Fungi, and would necessarily be included in a general survey. Others again are confined to individual groups and can only be fully discussed with them. At the same time we shall, I believe, get a clearer view of the whole subject ifthe second series of characters is considered along with the first, and those points only are reserved for special description in Division II which are quite irreconcilable with such general treatment ; among these are especially questions concerning homologies and sexual relations which are still in many respects obscure and debatable and must be considered in each individual case. 1. DEVELOPMENT AND SCATTERING OF SPORES. Section XV. According to our present views on the origin of cells, every cell is the daughter of a mother-cell, and except in the cases of conjugation and rejuvenescence is formed by a process of division which takes place in the mother-cell*. Either all 1 I pass over for the present the conjugation and coalescence of cells for reasons of convenience which have been partly intimated above; this subject will be considered in Division II. Reju- venescence I exclude because it is not the formation of a new cell, but only the transformation of a previously existing cell. = CHAPTER III.—SPORES OF FUNGI. 61 the constituents of the mother-cell enclosed within its cell-wall take part in this process, and the whole of the mother-cell is parcelled out into daughter-cells, or one portion of protoplasm only including the nucleus is separated from the other parts _ and applied to the formation of daughter-cells, while the remainder is not used for this purpose, but is subsequently turned to account in some other way. The former process bears the traditional name of ce//-division; the latter, from an original misapprehension, is termed free cell-formation. ‘The expressions /o/al and partial division would better describe the phenomena as they are understood at the present day. © ? Both modes of cell-formation occur in the formation of the reproductive cells which we are considering ; in the majority of cases the division is total. Asci afford beautiful examples of the so-called free cell-formation. In some cases, as in the formation of the spores of Mucor and the Saprolegnieae, it may be a question to which of the two types they belong. Excepting such doubtful cases, all cases of total division are cases of bipartition with formation of firm partition-walls. Of the details of the process of division we know no more than we know in the case of the division of vegetative hyphae ; we can only say that a partition-wall makes its appearance. The following are the chief modes of formation of spore-mother-cells and spores, distinguished from one another partly by the differences which have just been indicated and partly by peculiarities of form which present themselves in the process of division. Section XVI. 1. Intercalary formation (Intercalare Bildung). A delimitation (Abgrenzung) takes place of portions in the growing hyphae, and the cells constituting them become distinguished by their form and structure, acquire the characters of spores or spore mother-cells, and at length become free by the gradual decomposition or swelling of the parts that support or connect them. Their position is not uniform in the cases that are known to us. Normal formations of this kind are the resting spores of Protomyces, Cladochytrium, the spores of Entyloma, and the not infrequent cases of the formation of gemmae already briefly mentioned ?. 2. Acrogenous abjunction® (Acrogene Abgliederung). Delimitation of the extremities of hyphal branches with limited growth takes place by means of trans- verse septa for the purpose of forming reproductive cells, which are therefore placed, at least during their formation, at the apex of a stalk or sporiferous structure named since Léveillé dasdium or sterigma(ascus suffultortus of Corda). In more highly differ- entiated species the basidium is the peculiarly formed terminal cell of a hyphal branch, and the spores are frequently the extremities of slender stalk-like ramifications of this cell. In this case the actual stalks of the spores are termed sterigmata in a narrower 1 [See the sections in which the Mucorineae and Tremellineae are described. 2 The distinction between ‘ Abgliederung’ and ‘ Abschniirung’ (see section XVII) finds no ex- pression fin English botanical terminology, whilst*the idea implied in both has been rendered by the term ‘abstriction.’ If this term could be restricted to what is designated by ‘ Abschniirung,’ it might be retained as satisfactory; but unfortunately it has come to be used so generally in the sense of ‘ Abgliederung,’ that to avoid confusion it is altogether discarded in the text and the term ‘ abjunction” (with the verb to ‘ abjoint’) is introduced as rendering ‘ Abgliederung,’ and ‘abscision’ (with the verb to ‘ abscise’) is used to express ‘ Abschniirung.’] 62 DIVISION I.—-GENERAL MORPHOLOGY. sense of the word and the cell from which they spring is the basidium. In species of more simple character both expressions are used according to convenience. Among the manifold variations in individual cases which must be left for special description there are at the same time a number of generally recurring phenomena according to the mode of abjunction, the numerical relations, and the ultimate shedding of the abjointed portions. As regards the form which may be exhibited by the phenomenon, the cross septum may appear beneath the apex of the sporiferous cell, the apex itself being usually expanded: the portion thus delimited is the spore; the breadth of its base is about equal to that of the sporiferous cell. The simplest examples are most uredospores (Fig. 26) and the teleutospores of Uromyces. A second case is that in which branches grow at certain points from the sporiferous cell and these are either abjointed at the point of insertion, which usually becomes much constricted after the manner of the fae — eee i£5 ett, mrs: pestis icsssn YES ie _ FiG. 2. Puccinta gramints. FIG. 27. a—d Auricularia Auricula Fudae, Development of basidia and spores; Small piece of a hymenium; successive stages of the development according to the letters. a@ cylindrical terminal cell - uresdospores with four germ-pores ~ of a hypha from which several basidia are formed by transverse division 6; each of the in their equator, ¢ a pair of teleu- basidia puts out a long narrowly conical sterigma (c, @) from its upper extremity, and the tospores, the upper with a germ- swollen apex of the sterigma is abjointed as a spore s; x a sterigma from which the spore pore in its apex. Magn. 390 times. has fallen. /the development of the basidia of Exidta spicudosa, Sommerf.; four basidia are formed from the cell f by divisions crossing one another in the cell; the other parts of the figure show younger and later states; sa spore. The dotted lines indicate the surface of the hymenium. /after Tulasne highly magnified. a—d magn. 390 times. sprouts in the species of Sprouting Fungi (p. 4), or they elongate into slender stalks, sterigmata in the narrower sense mentioned above, and their swollen extremity forms by abjunction a spore. Examples, to be again noticed, are to be found in the Basidiomycetes, in Eurotium, Penicillium, Haplotrichum, Peziza Fuckeliana, &c. Intermediate cases occur, as might be expected, between the extremes and require no further description. A sporiferous cell or basidium may produce only one reproductive cell ba ie acro- genous abjunction, or several, even many, may be formed. ‘The first is the case in most species of the former of the two cat@gories just mentioned, for instance in the uredospores of Puccinia, Uromyces, and others. The basidia of Entomophthora are examples of the second case, and those of most species of Tremella, Exidia, and Auricularia Auricula Judae with long perieen- spent the swollen apex of which becomes a spore by abjunction (Fig. 27). he i ee ee ee ee CHAPTER III,—SPORES OF FUNGI. 63 - The acrogenous abjunction of the greater number of propagative cells is either simultaneous or successtve. It is simultaneous when a number of shoots make their appearance at the same time at the apex of the basidium, grow with the same rapidity, and experience abjunction at the same time, either at their point of insertion or beneath their apex which is borne by the stalk (sterigma). The protoplasm of the basidium is used up in the process and is not again renewed. Simultaneous abjunction is especially characteristic of the basidia in the hymenia of most Basidiomycetes (Hymenomyce- tes, Gastromycetes (Figs. 28, 29), Calocera, Dacryomyces). The basidia in these are generally club-shaped terminal cells of hy- phal branches, and spores are abjointed at their broad apices, usually as the extremities of long ~ sterigmata, more rarely as sessile FIG. 2& Octaviania carnea, Corda. Thin sections through the hymenium. 4, é basidia, one of them with two spores in the act of forma- sprouts of elongated or rounded _ tion, 4 paraphyses.. Magn. 390 times. shape, as in Geaster hygrome- tricus, Scleroderma, Polysaccum, and Phallus.“ The number of spores is in the large majority of cases 4 to each basidium, in some cases 2, as in Calocera, Dacryomyces, some species of Hymenogaster and Octaviania, in a few cases 6-9, as in the Phalloideae, Geaster, and Rhizopogon. Slight variations from these regular . numbers are not unfrequently found, especially in the species which do not form four spores on each basidium; in the Hymenogastreae, as in Hymenogaster Klotzschii, basidia are found which form only one spore. FIG. 29. Basidia of Gastromycetes on their basidiophores. a basidia of Geaster hygrometricus with eight sessile spores. 6 four-spored basidia of Lycoperdon pyriforme. _ c four- to eight-spored basidia of Phallus caninus. Magn. 390 times. Outside the group of Hymenomycetes basidia which produce many spores simultaneously occur in a great variety of forms on many gonidiophores, as in Peziza Fuckeliana, Botryosporium, Haplotrichum, and Gonatobotrys. The number of spores - abjointed is normally higher in such cases than in the Basidiomycetes ; they are usually placed close together on short stalks, so that-we may speak of spore-heads formed simultaneously. The typically unicellular branches of Peronospora which abjoint gonidia may be included with the above, especially if we take into consideration the form distinguished by Cornu under the name of Basidiophora. The simultaneously plurisporous basidia of the Basidiomycetes are usually more or less broadly club-shaped before the formation of spores, as has been already 64 DIVISION I,—GENERAL MORPHOLOGY. — ~~ said; in Calocera and Dacryomyces they are cylindrical thin-walled cells rich in finely-granular protoplasm, which either entirely fills their inner space or is interrupted by vacuoles. It may be assumed that there is a nucleus always present, though in the smaller forms it has been looked for in vain up to the present time. Where it has been observed, as in Dacryomyces, Calocera, Corticium calceum, and especially in the basidia of Corticium amorphum (Fig. 30) which become #mm. in length, it is a spherical weakly refringent body (perhaps the nucleolus), lying in about the centre of the cell. It is not to be seen in the early states of the basidium, and it disappears when the formation of sterigmata commences. More exact investigation into its behaviour in spore-formation has yet to be made. When the basidium has reached its full size, the sterigmata make their appearance on its rounded apex as narrow subulate sprouts, and when they have arrived at a certain length their extremity, which up to this time is finely pointed, swells into a vesicle which gradually acquires the form, size, and structure of the mature spore. As the spore advances to maturity the protoplasm of the basidium passes into the swollen extremities, FIG. 30. Corticium amorphum, Fr. Development of the spores, the successive stages being in the order of the letters. @ a nearly mature basidium with cell-nucleus. basidium with two ripe spores, two others having already dropped off. Magn. 390 times. and at length, when the spores are nearly matured, the delimitation of them by cross septa takes place; the basidium has by this time given up the largest part of its protoplasm, but retains a thin parietal layer and is still turgescent. A clear central spherical portion may be distinguished in the young fresh spores of many species ; it remains to be determined whether this is a nucleus and has proceeded from the nucleus of the basidium. The point of abjunction of the spore is either exactly at the apex of the sterigma or a little below the apex at a bend turned outwards (Fig. 30), so that the spore when detached takes with it the apical portion of the sterigma as a short stalk, or in a few cases, as in Bovista and some species of Lycoperdon, abjunction occurs at the point of insertion of the sterigma, which is consequently attached as a long stalk to the spore when the latter becomes free. In the cases mentioned above, where there are no sterigmata, abjunction as far as is known takes place in the way described. Arthrobotrys (Fig. 21) will serve as an example of another form belonging to this category. ey eS ee eee ee a CHAPTER I1II,—SPORES OF FUNGI. 65 In basidia exhibiting successive abjunction of many propagative cells the process of abjunction is repeated several times on the same basidium. There are three very distinct sub-forms of suceesstve aljunction, each of which has some special pecu- liarities connected with it, These sub-forms may be distinguished as the sympodial and the serzal or concatenate (Reihen-weise, Kettenweise), the latter being again divided into the smple and the branched. In the successive sympodial form (Figs. 31, 32) a single acrogenous spore is first of all abjointed from the extremity of the basidium or sterigma, which is always finely pointed. Then a new protuberance sprouts forth close to the point of insertion of this first spore, pushes it on one side and occupies the extremity of the sporophore, and is there abjointed as a new spore.’ A like proceeding may be repeated many times ; the last spore formed is always at the apex, and its older sisters are ranged on the same plane or one after another below the apex. In very extreme cases the * FIG. 3%. Dactylium macrosporum, Fr. Extremities of spori- FIG. 32. Botrytis Bassi, Bals. @ end of a ferous hyphae. @ ina dry state with a head of spores above. 6 young sporiferous hypha ; short lateral branchlets in water with the primordia of the youngest spores s at the have successively abjointed each 1-4 round spores. extremities of the branches, the small unevennesses beneath 6 end of an old branch which is producing spores being the points of attachment of the older spores which have by abjunction and is thickly covered with spores, become detached in the water. Magn. 300 times. the youngest of which are terminal. ¢ two sporo- genous branches, from which all the spores "have fallen with the exception of the youngest, and uppermost. @ magn. 390, 6 about 700 times. See Bot. Ztg. 1867. om spores are very soon entirely detached and either fall off or remain adhering only to the- one last formed, as happens in the formation of the gonidia of Epichloe typhina, in Claviceps and in the forms known by the name of Acrostalagmus of Corda. In other cases, as Botrytis Bassii and the small gonidia of species of Hypomyces and Hypocrea’, each spore arises at least far enough above its predecessor for the points of insertion to occupy some space, and the spores therefore remain united into sympodial successive heads. If the spores are detached, their insertions form slight projections or even short stalks at the extremity of the sporophore (Fig. 32). If the sporophore were to elongate between each pair of spores a sympodial arrangment would be produced, like that of Phytophthora in Fig. 20. 1 Verticillium agaricinum and its allies, Trichoderma viride, &c. See Tulasne, Carpol. ITI. [4] F 66 DIVISION I,—-GENERAL MORPHOLOGY. In the semple successive serial or concatenate forms the abjunction is repeated beneath the insertion of each propagative cell in the same direction and in the same form as in the case of the first cell, If the line of abjunction in that case was broad and transverse, the extremity of the sporophore beneath the youngest spore elongates to a definite extent and abjunction again takes place by formation of a new trans- verse wall; if the first sprout which becomes a spore has a constricted insertion, then after each abjunction a similar sprout with constricted base is developed beneath it from the persistent end of the sporophore and in turn undergoes abjunction. In this way a chain of similar segments is produced, in which the cells are ‘younger in proportion as they are nearer to the extremity of the sporophore from which they are ~ formed. The number of cells in a chain may be considerable, 20-30 or more. Examples are to be found in the gonidia of most of the Erysipheae, Cystopus, Penicillium, Cordyceps, and the Aecidieae, in the uredospores of Coleosporium, Chrysomyxa, and many others (Fig. 33). Branched serial or concatenate forms arise when one or more outgrowths stand- ing side by side on the apex of a filiform sporophore are abjointed, and then by repeated abjunctions produce a structure not unlike one of the Sprouting Fungi (Fig. 3). The first sprout-cell puts out one new protuberance from the apex which is remote from the sporophore, and this new cell and each succeeding one can do the same; a row of cells is thus formed in which the members are succes- sively younger as the apex is approached. Each of them can then form one or more toe eta Oh eet Ta tyibjuactons thefges lateral sprouts below its apex which adjoins is further explained in the text on page 69. 4 Eurotium Asper- . Situs glaneus;’> end of a sporophore covered with radiating the Cell next above it, and these new cells sterigmata, on which the formation of spores is just beginning. : oes and isolated portions showing single sterigmata gp with ther @Nd their progeny are similar to the first spores; # youngest spore of = chain. ¢ maga. so the rest 9 (Fig, 34), According as the lateral sprouts on cells of successive orders are placed singly or in a whorl of two or more members, chains are produced in which the branches vary in number and form. The cells of all orders are so many repro- ductive cells which are similar to one another in all important points and become ultimately detached from one another. Examples of this kind occur in the forms named by Fresenius? and Riess* Periconia, in which sprout-chains are collected together into a compact head at the extremity of a filiform sporophore, and in the small gonidial forms of Pleospora and species of Fumago and its allies in the Sphaeriaceae *, 1 Beitrage. 2 Bot. Ztg. 1853. * Tulasne, Carpol. II. CHAPTER III.—SPORES OF FUNGI, 67 of which those named Cladosporium herbarum, Dematium herbarum? and Alternaria are the best known; to these may be added the delicate heads of Myriocephalum botryosporum? and many others. Connected with these three kinds of acrogenous abjunction of spores is one which is less distinctly marked and which may be termed the mode of cross- septation (Querzergliederung). In this the terminal por- tion of a hypha or hyphal branch grows first of all to a certain length, and then ceases to elongate but is divided by cross septa into a number of spore-cells. This mode of formation is seen most distinctly in the sporogenous branches of strong specimens of Oidium lactis* which rise into the air above the substratum. These branches have a cylindrical form and are many times longer than broad. When they have ceased to elongate they quickly divide by formation of cross septa into numerous cylindrical spores which are from one to two times longer than broad. In small specimens this cross-septation may extend over the whole plant, occur- ring even in the branches of the mycelium in the substratum. ‘The formation of cross septa appears to commence in stronger individuals at the free apical extremity and to advance basipetally; but this point is quite as uncertain as the question, whether the sporo- genous branch consists at first of a number of longer cells which are afterwards divided into the short members by repeated intercalary bipartition, or whether the latter are the first divisions formed either simultaneously or successively and in basipetal order in the branch which was up to the time of their formation unicellular; on these points further examination of the branches of this Oidium is to be desired. Of similar character are the gonidial mother-cells of Syncephalis and Piptoce- phalis*, which spring simultaneously from the apex of the capitate extremities (basidia) of the sporophores and form a small clustered head. They have the form of elongated cylinders with rounded apices, and are divided after they have ceased to grow in length into several FIG. 34. Species of 4iternaria. a and 6 extremities of a sporiferous hypha growing obliquely into the air from a specimen grown on a micros@opic slide, a on the 4th Aug. at midday, some 23 hours later; the two rows of spores which are still simple in @ are branched in 4. ¢ a young sporophore on a my- celial filament submerged in water. The membranes of the pointed ovoid spores are yellowish brown where they show partition-walls in their interior and are colourless only at the upper pointed extremities. This is the case also with the youngest and still small spores, the sporophores and the mycelium. a and 4 magn. about 145, ¢ 225 times. — se See eC SC CUrThU TC short cylindrical spores by transverse septa formed either simultaneously or succes- sively and in basipetal order, but always very rapidly. 1 Low in Pringsheim’s Jahrb. VI, p. 494. Penicillium cladosporioides, P. viride, P. chlorinum, all of Fresenius (Beitr.), and P. olivaceum, Corda, are evidently the same form. Even if Tulasne’s view that the plant belongs to Pleospora herbarum is not confirmed, its connection with one of the allied Sphaeriaceae is more than probable. 2 Fresenius, Beitr. t. V. ’ Fresenius, Beitr—Brefeld, Ueber Gahrung in Thiel’s Landw. Jahrb. V, 1876, t. II. * De Bary und Woronin, Beitr. II. Brefeld, Schimmelpilze, I. Van Tieghem et Le Monnier in Ann. d. Sc. nat. Sér. 5, XVII, p. 370. See also below, sect. XLIII, Fig. 74. F 2 68 DIVISION I.—-GENERAL MORPHOLOGY. The spore-formation in Ustilago and Geminella, which will be further considered in section LV, appears from Winter's observations on Geminella and Ustilago Ischaemi? to be nearly allied to the cases just described. More certainly is this the case with many acrogenously formed so-called sep/a/e spores, as those of Puccinia (Fig. 26 /) and Phragmidium, and many forms of Hyphomycetes, the systematic position of which has not yet been exactly determined, Trichothecium, Arthrobotrys Fusiporium, &c.; also forms which we now knowas gonidiophores of the Pyrenomycetes, such as Fries’ groups of the Dematieae and Sporidesmieae, Helminthosporium, for example, Cladosporium, Alternaria, Sporidesmium, Phragmotrichum, Polydesmus, Melanconium, Stilbospora, Coryneum, Exosporium, and very many other forms. See Figs. 21 and 34, and section XXIX. Section XVII. The inception (Anlegung) of acrogenously produced spores takes place in every instance according to one or other of the processes which have now been described. In some also ripeness, that is the capacity for further normal develop- ment, and the size, form, and structure which indicate this capacity, is reached, as has been repeatedly stated above, when the delimitation is completed. This is the case, for example, in Cortictum amorphum (Fig. 30) and in many, perhaps in all the Basidiomycetes, and to a certain degree in Cystopus Portulacae (Fig. 33); in the case of many other small spores attached by a very narrow stalk it is not possible to speak with certainty on this point, because the minuteness of the point of insertion renders it impossible to determine the exact moment when delimitation by the cross septum is effected. On the other hand, many cases are known in which after acro- genous delimitation the cross septum undergoes a considerable amount of growth before it is mature, and it obtains the necessary food for this purpose from the sporophore ; this is the case, for example, in all the species of the Uredineae mentioned in the pre- ceding sections, and in Eurotium and Penicillium, &c. In a rapidly growing successive chain in these species the majority of the younger members are still immature, and the nutrient material, so far as it comes from the sporophore, must pass by the younger cells to reach the older more distal ones. . Many acrogenous spores are fersts/ent on the sporophore after they are mature, and are carried away from the place where they were formed only by accidental external mechanical agencies, as the teleutospores of Uromyces, Puccinia, and Phragmidium, the large gonidia of Hypomyces and many other septate forms above mentioned. But the larger part of these spores are de/ached from the sporophore as soon as _. they are mature by the aid of internal causes, which during the process of ripening bring about certain changes in the original condition and thus render the ultimate separation possible. The three chief modes known to us in which this purpose is effected are the disappearance of the sporiferous structure (Schwinden der Trager), abscision® (Abschniirung), and adjection* (Abschleuderung). The disappearance of the sporiferous structure is most common among the Gastromycetes, in which, when the spores are ripe, not only the basidia, but usually 1 Flora, 1876, Nr. to, 11. ? See note on page 61. ® See note on page 84. a CHAPTER III.—SPORES OF FUNGI, 69 also the rest of the hymenial tissue, becomes entirely dissolved by processes of decom- — position not accurately known, and the spores are thus set at liberty. They lie at first in the place where they were formed; their subsequent fortunes are described in Division II. The history of the basidia, which make their appearance as branches of the simple sporophores and form gonidia in Peziza Fuckeliana (‘Botrytis cinerea’), is essentially the same. They disappear entirely after the gonidia are ripe, and the latter cling in loose heaps to the place of their formation. The process of abscision is the most common of the three and appears with the greatest variety of forms. Generally a transverse zone between the adjacent cells disappears or grows soft, and their separation is thus effected or made easy, The transverse zone which disappears is either a middle lamella of the cross septum between the two cells or it is a small stalk-cell, which is cut off from the young spore by a cross septum and then dis- appears, as in the uredo-chains of Coleo- sporium and Chrysomyxa and all the Aecidieae. ‘The changes observed in the zone of separation are in one series of cases simply that it becomes gradually smaller and especially narrower and _ at length entirely disappears; in other cases it swells up into a jelly and becomes disorganised. The product of the swelling may in the latter case be persistent, and is then usually increased to a considerable extent by the gelatinisation of the lateral walls of the spores, which are therefore ultimately glued together by a gelatinous mucilaginous gummy substance ; in other cases the products of disorganisation at length entirely disappear, and complete Fic. 3s. @ Cystopus Portulacae; m mycelial branch bearing isolation of the spore is effected. It is igor raphael daiggens Servs fh prenis natural to suppose that this process de- Seen ae tacmns of cares teil Cael tones scribed as disappearance consists in a — myoungestspore ofachain. “a mage ayn che rest go tinees | transformation into soluble compounds and a simultaneous osmotic absorption of these into the adjacent cells, especially in the many cases in which the spore about to be removed by abscision continues to grow while the disappearance is proceeding, and would seem therefore to be receiving more food, In some cases one might also suppose a process of com- bustion. Precise statements on these points are not possible in the present state of our knowledge. : These phenomena are well exemplified in the.simple successive gonidial rows in the genus Cystopus, especially in C. cubicus and C. Portulacae (Fig. 35 a), which latter plant is more particularly referred to in this place. Delimitation of the rounded apical portion of the basidium (J) is effected by a broad cross septum to form a gonidium (7). 7° DIVISION I.—GENERAL MORPHOLOGY. The septum appears first as an annular ridge on the inner side of the lateral wall of the basidium, and grows slowly into a plate of considerable thickness which is convex on the side towards the basidium and correspondingly concave on the other, and shows the bluish lustre of gelatinous membranes under the microscope. When it is fully formed the apex of the basidium elongates to form a new gonidium. The new portion thus formed is close under the transverse septum. In correspondence with the subsequently rounded form of its apex it is from the first somewhat narrower than the septum, and by its elongation it separates the septum at its margin from the lateral wall of the basidiurfi and carries it upwards with the goni- dium to which it belongs. Each gonidium accordingly has its slightly convex surface resting at first on its younger sister with the margin free, but attached to its apex by the broad middle portion. The gelatinous cross septum, to which the whole of the surface of attachment belongs, is continuous above with the lateral wall of the gonidium; and while this becomes slightly thickened as it developes, a membrane, which is not at first clearly defined, is formed on the inner surface of the septum and is also continued into the lateral wall which it resembles in appearance; this is the persistent basal wall of the goni- dium. At the same time the original gelatinous transverse septum begins to disappear from its margin inwards as if it melted away. There is now in all beyond the third and fourth youngest gonidia of a row only a quite narrow in- termediate piece in the middle connecting each with its younger sister. This piece is of about the same height as the original septum, but the bluish glistening substance in it dwindles from below upwards into a small plate which becomes continually thinner and remains attached to the wall of the gonidium to which it belongs. As this process goes on the intermediate piece becomes pale and very slightly refringent, and after persisting for some time in this state at length disappears. There is no reason for Z a regarding this delicate intermediate piece as a part of an outside membrane which covers the whole gonidial chain FIG. 36. Penicillium giaucum. ikke a sheath, as I formerly did. The single gonidia show @ young gonidiophore with the com- 5 mencement of successive serial ab- no jmportant changes after they are detached from the Ge truaies dng nargea heat gonidiophore beyond the thickening of their membrane aaa aoe treatment witk alcehot alteady mentioned, which cannot be further pursued here. and glycerine. Magn. Goo times. Most of the propagative cells formed by acrogenous abjunction which have now been mentioned are detached by abscision in the manner described above, and, like the cells of Sprouting Fungi, they must become detached by disappearance of an original intermediate lamella just as is observed in Cystopus. Careful examination shows indications of this in almost all cases; but the details of the proceeding are often difficult to follow on account of the too small size of the parts, yet it can be seen very distinctly, in spite of their small size, in the successive gonidia-rows in Eurotium and Penicillium, not- withstanding their minuteness (Figs. 35 4 and 36). Some further details may be seen in Zalewski’s treatise, mentioned at the end of this chapter. In a certain number of forms the separation is effected by the formation of a gelatinous or gum-like deliquescent substance both on the surface of separation and on the rest of the circumference of the spore. It must be supposed that this substance also is the product of an outer lamella of the spore-membrane which was not originally gelatinous ; but the minuteness of the objects: prevents this from being certainly ascertained. With the ordinary amount of moisture necessary for the growth of Fungi the deliquescent substance absorbs so much water that the spore when abjointed is easily detached; a drop of water washes it away at once, ~ CHAPTER III.—SPORES OF FUNGI. 71 if kept dry it will continue to adhere to the gonidiophore. Spores abjointed close together in large numbers cohere through the coalescence of their gelatinous envelopes and form masses which break up again in water. In the case of spores successively abjointed on the free apex of one or several closely adjacent sterigmata, if the development takes place without interruption in a damp atmosphere, the gelatinous substance deliquesces and forms a spherical drop, in which the spores lie embedded as in a vesicle. And all this occurs alike in those cases where the successive abscision affects spores arranged in rows (gonidia of Nectria Solani’) and in those where they are in heads (Acrostalagmus cinnabarinus, gonidia of Claviceps and Epichloe). Where abscision of large numbers of spores ‘takes place inside narrow receptacles provided with narrow orifices, their release from the receptacle is effected by the formation of a gelatinous or gummy substance which swells in water and emerges with the spores from the receptacle. Examples are to be seen in numerous gonidia- receptacles in the Pyrenomycetes. See Division II. A description of the development of the spore-chains in the aecidium of Chrysomyxa Rhododendri? will show the mode in which the spores are shed in the Uredineae by the solution and disappearance of a stalk-cell or in- termediate cell beneath each spore. The spores in each chain are formed by successive abjunction at the upper extremity of a short club-shaped basidium, from which at first an almost cylindrical spore-mother-cell is abjointed by a plane transverse septum. This cell, which is about one and a half times longer than broad, subsequently changes its shape; one side bulges considerably, the other only slightly, and the whole cell thus becomes irregularly barrel-shaped. It is then divided into two unequal daughter-cells by a plane partition-wall which runs from the angle formed by the basal cross septum . and the more prominent side obliquely towards the flatter side, cutting off the lower third part of it; the lower of the two daughter-cells is a small wedge-shaped stalk-cell or intermediate cell, the upper is larger and developes into a spore. The spore is at first of a some- what complex and irregular form, as is sufficiently apparent from what has been said above and from the Fig. 37. It FIG. 37. Chrysomyxa Rhododen- increases considerably in size, assuming in so doing a fon an accion: nearly spherical or ellipsoid figure, and becomes invested ‘he text. Magn. 6oo times. with a new membrane of considerable thickness, into the structure of which we must not at present enter. The stalk-cell grows at the same time in height and breadth, remaining much lower on the side where its wedge-form thinned out originally than on the opposite and now convex side, and has an elliptic transverse section. Ultimately the stalk-cell disappears, its membrane and the outer primary lamellae of the membrane of the mother-cell and of the transverse septum swell up, become gelatinous, and finally vanish entirely with the cell-contents, and the spores are now isolated. The division into stalk-cell and spore is usually found in the third youngest spore-mother-cell on a basidium, more rarely in the fourth youngest. The gelatinous dissolution of the stalk-cell is usually far advanced in the 1 De Bary, Kartoffelkrankheit, p. 41. Reinke und Berthold, Die Zersetzung d. Kartoffel durch Pilze, p. 39. ? Bot. Ztg. 1879, p. 803. 72 DIVISION I.-—GENERAL MORPHOLOGY. one belonging to the sixth youngest spore in the chain. Phenomena essentially the same occur in other species of the Uredineae, but with considerable variations in form in the different species’. Where filiform sporophores rise free into the air, a further mechanical arrange- ment is found which greatly assists the shedding and scattering of the abscised spores. It may be readily observed in the Hyphomycetes, in Peronospora, for example, Phytophthora infestans, and in the gonidiophores of Peziza Fuckeliana, &c. The hyphae of these Fungi are cylindrical in the ‘moist and turgescent state, but collapse when dry and especially when the spores are ripe into a flat ribbon-like form’, and the drier they are the more strongly do they become twisted round their own longitudinal axis. They are so highly hygroscopic that the slightest change in the humidity of the surrounding air, such for instance as may be caused by the breath of the observer, at once produces changes in their turgescence and torsion; the latter give a twirling motion to the extremity of the gonidiophore and the ripe spores are thereby thrown off in every direction. Abjection of acrogenous propagative cells is effected by a mechanism which we shall have to speak of again in section XXI. The cell which is to be abjected, whether spore or spore-mother-cell (for brevity we shall call it spore), is abjointed singly by a cross septum at the apex of a tubular and often comparatively large sporiferous cell, a basidium or a sterigma, which retains its parietal protoplasm still intact after the abjunction of the spore and is still turgescent in consequence of a continued atlases. sc supply of water in increasing quantity. Its membrane = Saw drape Pig shyt is highly extensible and elastic, and continues to stretch eect oe See eS Oe the tension increases with the increased amount of Beans Die te owes ot Gs EL absorbed. But its cohesion is less over an annular area immediately beneath the cross septum than in any other part of the circumference, and if the tension reaches a certain point, it overcomes the resistance of the less coherent annular zone, the su/ure of dehiscence; the wall opens by a circular fissure, the pressure of turgescence is instantly relieved and the elastic wall contracts, especially in the direction of the transverse diameter, and this causes a large part of the fluid contents to be squirted out at the same moment with force through the fissure, and as it strikes full on the transverse septum, the spore that rests upon the septum is abjected with it. The basidium thus emptied collapses and perishes, The process of abjection may be observed most completely in the acrogenously abjointed spore-mother-cells of Pilobolus crystallinus and its nearest allies, of which we shall speak again in later sections (Fig. 38). It occurs also, as Brefeld® has ? Bot. Ztg. 1. c. p. 786. De Bary, Brandpilze, p.59. Reess, Rostpilzformen d. Coniferen, Halle, 1869. R. Hartig, Wichtige Krankh. d. Waldbaume, t. IV, V. ? Fresenius, Beitr. t. II. * Bot. Ztg. 1870, p. 161. Abhandl. d. Naturf. Ges. zu Halle, Bd. XII, 1. 1871. NO a - CHAPTER III,-~SPORES OF FUNGI, — : 73 shown, in the basidia of Empusa and species of Entomophthora. The ripe spores are thrown to a distance of 2-3 cm. and adhere by the remains of the ejected proto- plasm to the bodies against which they strike. The ripe spores of Coprinus, especially C. stercorarius, are abjected from the basidia by the same mechanism, as Brefeld informs us’. They are attached, as Fig. 30 shows in the case of other Hymenomy- cetes, to the extremities of very slender sterigmata which spring four together from the apex of a basidium. The four spores of each basidium are abjected at the same moment, and a small drop of fluid which issues from the sterigma shows that it is open at the apex, while a small quantity is also seen to be attached to each spore as it drops. The similarity in the basidia and in the mode of formation of the spores in all the Hymenomycetes and other facts also make it probable that the process of abjection is widely. spread, perhaps occurs universally, in this group of Fungi; but more extended investigations are still needed to clear up this point. The following are some of the other facts just referred to. It has long been known that the hymenium of a Hymenomycete when turned upwards becomes gradually sprinkled over with free spores, and if it is turned downwards, spores fall from it in large quantities. Some of them fall in an exactly vertical direction, as appears from the fact that the spores which fall on a piece of paper placed under the free hymenium of an Agaric are arranged in radial lines answering exactly to the radial arrangement of the lamellae on the pileus. These phenomena are in themselves quite compatible with simple abscision as described in the preceding pages, but they do not exclude the supposition that the spores were abjected with some small exertion of force, as Brefeld has also pointed out*. On the other hand a dispersion of the spores is observed in these Fungi in other directions than that of the vertical. The statement of Bulliard* has recently been confirmed by Hoffmann and de Seynes, that many spores fall from the hymenium of an Agaric when turned downwards far beyond the line which corresponds to the margin of the pileus. Hoffmann saw white clouds of spores rise like smoke from Polyporus destructor when there was a slight movement in the air, ‘but when the air in the closed chamber was perfectly still no spores reached a glass plate hung at a distance of only three quarters of an inch above the plant, while those which fell on a glass plate two inches and a half beneath the Fungus covered nearly uniformly up to the margin a space of more than six times the circumference of the Fungus.’ Other Hymenomycetes gave similar results. These observations point to abjection of the spores, but do not absolutely prove it, because the facts described might be due to movements of torsion in the sterigmata, such as were noticed above on page 72. Lastly, it may be observed that the abjection of the spores in Leitgeb’s Completoria * ‘may also have been caused by the mechanism which has already been described ; Leitgeb’s own explanation I have not been able to understand. Section XVIII. 3. Endogenous spore-formation (Endogene Sporenbildung), Many spores are produced inside mother-cells, the wall of which remains intact till the spores are ripe and forms a spore-receptacle or sporangium. The sporangia are mostly acrogenous cells which are either persistent on their sporangiophore, or are removed from it by abscision, as in Cystopus and other ' Schimmelpilze, III, p. 65. 2 Tb. p. 132. * Champignons de France, I, p. 51. * Sitzungsber. d. Wiener Acad. Bd. 84, July, 1881. 74 DIVISION I.—--GENERAL MORPHOLOGY. Peronosporeae; more rarely they are intercalary. Their spores are produced by division without formation of parting walls and conform to two chief types: 1. A parietal layer of protoplasm at least is not included in the division and is left behind in the sporangium, as is the case in asci. 2. No parietal layer remains behind, as in the sporangia of the Phycomycetes, which show much variation in details. a. In the sporangia of the Phycomycetes the whole of the protoplasm, whether parietal and enclosing a vacuole or filling the lumen of the cell, is divided to form the spores. ‘The number of spores directly produced by the division is not fixed in any species except perhaps in Tetrachytrium’, and is often very large, as in Mucor, Pilobolus and large Saprolegnieae. The division usually appears to be simultaneous ; but Biisgen _ observed under very favourable circumstances in Leptomitus lacteus and Mucor that _ the protoplasm was divided by very rapid bipartitions into successively smaller portions up to the final formation of spores. When the division is complete the future limiting surfaces of the sporesare at first indicated by granular plates, but these are at once replaced by homogeneous delicate and narrow partition-layers, which often however become broader; these layers proceed probably from the blending of the grains and usually continue ofa soft gelatinous consistence, being directly transformed into plates of cellulose only perhaps in species of Dictyuchus. In the Mucorini and in Dictyuchus clavatus the spores which lie between such dividing layers become invested at once with a firm cellulose membrane; in other species a distinct membrane does not appear before the spore leaves the sporangium. The early stages of the division in Aphanomyces show exceptional deviations from the ordinary type. No growth of the spore when it has once been separated off takes place inside the sporangium in any of the above cases. The process of division may be observed in its greatest completeness in the sporangia of the larger Saprolegnieae which live in the water; in Saprolegnia, for example, Achlya and Leptomitus lacteus. The sporangium is a large club-shaped cell delimited by a transverse wall from-the unicellular tubular sporangiophore. It is densely filled with a coarsely granular protoplasm, or may have a large axile vacuole. Shortly before the division the protoplasm becomes everywhere uniformly and finely granular and has small inconstant vacuoles at wide distances from each other. It is then suddenly divided by granular plates, which look like rows of granules when seen in profile, into numerous polyhedral or polygonal portions, the future spores, which in Leptomitus, as was said above, are formed by rapid successive bipartitions. The partition soon becomes more pronounced, the partition-streaks which were before granular now become homogeneous, and no longer appear as fine clear lines but grow broader as the spores are rounded off. With this the separation of the spores is complete in the cases which we are considering: the substance of the partition-plate which is derived apparently from the granules that were previously present continues homogeneous, soft and capable of swelling. Colouring reagents, as Fr. Schmitz? first discovered, show the presence of a number of nuclei in the sporangium as soon as it is delimited, and a division of them afterwards. Each spore obtains a nucleus, which has been directly observed to proceed in Leptomitus from the division of the original nuclei. These processes which lead at once to the for- mation of spores are however preceded by other separations in which the behaviour of the nuclei has not been clearly ascertained. The coarsely granular protoplasm 1 Sorokin in Bot. Ztg. See also below, section LII. ? Sitzsber. d. Niederrhein. Ges. Aug. 4, 1879. CHAPTER III.—SPORES OF FUNGI. : 75 of the sporangium is first divided into portions resembling the future spores in number, position and size, and the division is effected by partition-plates which are at first granular in character and afterwards become broad hyaline stripes. These subse- quently disappear, and the whole of the protoplasm assumes the uniformly finely granular appearance described above, and at once proceeds to the final division. The same or very similar phenomena, and among them the preliminary transitory separation, have been observed in Dictyuchus monosporus, but there in place of the final partition-plates firm cellulose membranes are formed, from which the spores subsequently escape. In Dictyuchus clavatus each spore is invested with a membrane of cellulose, but is separated from its neighbours by a thin layer of a hyaline substance, which is soft and gelatinous in water and must be formed from the partition-plates ; it is still a question whether the membranes of the spores are obtained by differ- entiation from the plates, or are a later product from the spores themselves. In the Mucorini with endogenous spore-formation which do not grow in water (Mucor, Pilobolus, &c.) the processes of division cannot be followed throughout under the microscope; but whatever can be learnt about them from dead material agrees so closely with the final stages of division in the Saprolegnieae, and especially with those of Dictyuchus clavatus, that we are justified in assuming that the process of division is quite similar. At first the spores are delimited as polyhedric bodies by very narrow partition- plates: by and bye each is rounded off and invested with its own cellulose membrane, as in D.clavatus, and separated from the others by a layer of gelatinous substance that swells in water. In some species of Mucor (M. plasmaticus of Van Tieghem) this intermediate substance is largely developed’, occupying in the intact sporangium even more space than the spores themselves, and is finely granular. It may be doubted whether the entire mass is formed in such cases from the partition-plates ; it is possible that it is exuded from the spore-forming protoplasm before the division, or comes also in part from the membrane of the sporangium (see section XX). Our present investigations still leave the point unsettled. Preliminary separations have not been observed with certainty in Mucor. The description given above does not hold good of all the Saprolegnieae which have been examined, and is true of Phytophthora only among the allied Perono- sporeae. The only point in which all agree is in the ultimate appearance of the hyaline partition-plates with capacity for swelling, and this remark applies also to the Chytri- dieae ; some details with respect to the latter group which belong to this place will be given in section XLVI. Aphanomyces deviates from the Saprolegnieae to a greater extent than any other of the allied forms. The spores are cylindrical, three times as long as broad with rounded ends, and lie one behind the other in a single row in the slender cylindrical filiform sporangia. At the commencement of their formation the granular parietal protoplasm, which is from the first uniformly distributed but always remains parietal, aggregates into dense transverse girdles, which are three or four times as long as broad and are separated from one another by shorter hyaline transverse zones, in which only a very thin almost entirely homogeneous parietal layer of protoplasm remains attached to the membrane. When the granules originally distributed in coarse irregular streaks have become uniformly distributed in the thick girdles, annular constriction appears in the parietal layer in the middle of each hyaline transverse zone, and advances in the centripetal direction till the zone separates into halves which become absorbed in the adjacent thick zones. These at the same time have become spores, and are separated from one another by hyaline interstices filled probably with a substance which is less dense and more capable of swelling. The behaviour of the nuclei in this proceeding has not been investigated. Further details will be found in Biisgen’s treatise cited at the end of this chapter. 1 Brefeld, Schimmelpilze, I, 16, 76 DIVISION I.—GENERAL MORPHOLOGY, Section XIX. 4. The asci (thecae) are in almost all cases the solitary terminations of hyphal branches; several or many of these asci, in most cases a very large number of them, arranged nearly parallel to one another and with hairs (paraphyses, section XII) between them are grouped together to form hymenia, which in the Discomycetes are open superficial layers on the sporophores, but in the Pyreno- — mycetes are in the interior of receptacles (perithecia) which are either closed or provided with a narrow orifice. See sections LIX—LXII, where some account is given of the exceptions to the rule thus briefly stated. : The formation of the asci is not essentially different from that of other terminal cells of hyphal branches. They are generally club-shaped, more rarely broadly ellipsoid or are stalked spheres as in Tuber, Elaphomyces, Erysiphe, Eurotium, and others; and when once orientated they grow on usually without interruption till they attain their definitive shape and size and then in most cases begin immediately to form spores. It is only in some species of Erysiphe that the formation of spores is preceded by a longer period of rest ; it is indeed possible that young immature asci may pass through the winter period of rest in the case of speciés which, like Rhytisma and its allies, form their spores in spring, but this has never been directly observed. In the very large majority of cases eight primordia of spores are formed simultane- ously in each ascus; the facts connected with this proceeding were carefully investigated by myself in 18631 in certain species of Peziza, Helvella, and Morchella, by Strasburger ? recently in Anaptychia ciliaris, and by Fr. Schmitz* in species of the same genera and of Ascobolus, Chaetomium and Exoascus, with the following results. In a number of Pezizas (P. confluens, P., Fig. 39, P. pitya, P.) the young ascus is filled with finely granular protoplasm containing vacuoles; a nucleus may be seen in the centre of the protoplasm, as soon as the tube has reached about a third of its ultimate length, in the form of a clear spherical body, in the centre of which is another smaller and strongly refringent body. It has yet to be learnt whether the whole body should be called the nucleus and the inner and smaller body the nucleolus, or whether the latter alone is the true cell-nucleus. As the ascus elongates the protoplasm moves into its upper extremity, and the lower portion, which may constitute three-fourths of the whole length, now contains only a more watery fluid and a thinner parietal layer of protoplasm. When the ascus has reached its full length, the commencement of spore-formation is indicated by the appearance of two smaller nuclei in the place of the original nucleus. In a later stage four nuclei are seen and then eight; the nuclei are always of similar structure but their size diminishes as their number increases. Their arrangement and Strasburger’s observations on Anaptychia leave no doubt that they are produced by successive bipartitions from the primary nucleus. The eight nuclei of the last order are about equidistant from one another, and are each ultimately surrounded by a sphere of protoplasm, which is distinguished from the rest of the protoplasm by its greater transparency and has a very delicate line of delimitation. These portions of protoplasm ! Die Fruchtentwickelung d. Ascomyceten, p. 34. ? Bot. Ztg. 1872, p. 272. Zellbildung u. Zelltheilung, Aufl. 3, p. 49. ° See above on page-16. CHAPTER III,—-SPORES OF FUNGI, 77 are the commencements of spores; they are formed simultaneously and soon become invested with firm membranes, and grow as they lie arranged in a longitudinal row inside the ascus to about double their original size. The protoplasm which surrounds them at first disappears rapidly in Peziza pitya as they increase in size, and like the protoplasm contained in the spores is always coloured yellow by iodine in this species. The protoplasm of the ascus before the spores are formed, and that within the spores at all times, shows the same reaction with iodine in Peziza confluens. But after the orientation of the spores the protoplasm of the ascus shows the characters of a substance, for which I formerly proposed the name of eszp/asm, and which is dis- tinguished from ordinary protoplasm by being more highly refringent, by its peculiar FIG. 39. Pestza (Pyronema) confluens, P. aasmall portion of the hymenium; / a paraphysis, which is only attached to the hyphal branches from which the three asci spring without originating in them. »—vz full-grown asci, the successive stages of the development in the order of the letters ; in »—z the nuclei are multiplying, in v the spores are being formed, in w they are mature. 72 young asci.. Magn. 390 times. homogeneous and glistening appearance, and especially by the reddish brown or violet brown colour which it assumes when treated with very dilute solution of iodine. Errera! has recently shown that this reaction with iodine is due to the circumstance that the epiplasm contains a relatively large quantity of glycogen permeating a protoplasmic or albuminoid vehicle; the term glycogen-mass, or shortly glycogen, may therefore be substituted for that of epiplasm. In some other species with large asci (Peziza convexula, P. Acetabulum *, and P. melaena, Helvella esculenta, H. elastica, and Morchella esculenta) the contents of the ascus which are at first uniform are differentiated before the spores are formed into protoplasm and glycogen-mass, The former aggregates in Peziza convexula into a ' 1 See above on page 6. * The species named Peziza sulcata? in my work on the Asycomycetes belongs to P. Acetabulum. 78 DIVISION I.---GENERAL MORPHOLOGY. transverse zone lying in the middle of the ascus, or in most other species into a mass which fills the upper third or fourth portion of the ascus ; the remaining and especially the lowermost portion contains only the glycogen-mass which is marked by many vacuoles of varying size and arrangement. Sometimes, as in Morchella esculenta and Peziza Acetabulum, the uppermost portion: of the ascus above the protoplasm is occupied by a layer of glycogen, the protoplasm filling a cavity with a sharply defined outline in the glycogen-mass. The nucleus always lies in the protoplasm and in or near its centre, at which point the spores are formed in these as in other species, the mode of formation being essentially the same as that described above. The young spore-primordia are in contact with one another in Peziza convexula and Morchella esculenta. Only the first stage in the division and the ultimate eight nuclei, round which the formation of spores takes place at once, have been directly observed in most of the above species; the other stages have been seen only in Peziza convexula. But the accounts which we possess and observations on the formation and division of nuclei in other plants compel us to assume, that the process in the eight-spored ascus are essentially the same in all cases and that the successive stages in the division of the nucleus have simply been overlooked, owing partly to the rapidity with which the operation is effected and partly to difficulties of observation of other kinds. - Numerous independent observations on a considerable number of Diseomycetes with eight spores formed simultaneously in one ascus have established the presence of the primary nucleus before the formation of spores, the appearance of the young spores in the manner just described, and the occurrence or non-occurrence of differen- tiation of the glycogen-mass and protoplasm according to the species. There is therefore no reason to doubt, that the course of development above described prevails very generally in the group which contains the genera Peziza, Phacidium, Leotia, Ascobolus and Geoglossum. It is often difficult to follow it throughout in large asci, like those of Leotia lubrica, Geoglossum hirsutum, Helvella, &c., because the protoplasm of the young tube and of the spores is rendered opaque by the number of drops of oil. In very many other cases the minuteness of the asci and spores either prevents a complete observation or renders it difficult ; but even in these cases a little attention will enable us to see the primary nucleus, the simultaneous appearance of the eight spores as portions of protoplasm with a fine boundary-line, and sometimes (Sclerotinia sp.) a nucleus in each of them. In the small asci of e.g. Peziza tuberosa, P. Sclerotiorum, P. calycina and Phacidium Pinastri, and also in some larger ones, as those of Lecidella enteroleuca, Pertusaria lejoplaca, Lecanora pallida and Sphaerophoron coralloides, the primary nucleus appears as a strongly refringent roundish body, which is either homogeneous or more pellucid and as if hollowed out in the centre; the clear, trans- parent, spherical space is not or not always (Peziza Fuckeliana) to be seen through the periphery. It is more difficult to observe the formation of the spores in the asci of the Pyreno- mycetes containing eight spores formed simultaneously, than in the Discomycetes, on account partly of the minuteness and delicacy of the organs, partly of the presence of oil globules which are present usually in large numbers in the protoplasm. Yet careful observation shows that the spores are formed in the way described above. A nucleus has rarely been seen in them (Sordaria fimiseda, Fig. 52). An oil globule was often taken for a nucleus by older writers. The primary nucleus on the contrary may be distinctly seen in many species before the spores are formed; it has the characteristics of the nucleus of Peziza calycina and P. tuberosa which have just been described, and always lies in the same position a little above the middle of the ascus, for example in the nuclei of Xylaria polymorpha, Nectria, Sphaeria obducens, Curcurbitaria Laburni, Pleospora herbarum, Sordaria fimiseda, De Not., and some es ee ee CHAPTER III,—-SPORES OF FUNGI. : 79 others. The contents of the asci in most of the Pyrenomycetes which have been examined show only the yellow coloration of protoplasm with iodine; but the glycogen reaction is beautifully shown in Sphaeria obducens during or even before the formation of the spores, and in Pleospora herbarum, Sordaria fimiseda, and Sphaeria Scirpi after their formation. All these facts tend to show that the developement of the eight-spored asci in the Pyrenomycetes is essentially the same as in the Sisconty® cetes, and that further observations will confirm this view. The eight-spored asci of Podosphaera Castagnei have a large nucleus in the young state ; this subsequently disappears, and the spores which are formed simultaneously have very distinct central nuclei and are imbedded in a glistening glycogen-mass. Nuclei were found also by Fr. Schmitz in the asci and spores of Exoascus Pruni ; in other respects the development of the spore is entirely the same in this species as in the Discomycetes (see also section LX XVI). The number of primordia of spores laid down in the typically 8-spored asci is very constant; exceptions are comparatively rare, such as that of 9 spores in Cryptospora, Tul. and in Exoascus, and 13 developed normally in a single ascus of Peziza melaena. It more frequently happens, especially in the Pyrenomycetes and Lichen-fungi and accord- ing to Boudier in Ascobolus also, that some of the 8 spore-primordia remain unde- veloped ; most of the cases in which less than 8 spores have been found in species in which that is the typical number, may probably be thus explained. The abortion of individual spores is almost always an accidental phenomenon ; it occurs regularly, according to Tulasne’s account’, only in Collema cheileum, where the mature ascus always (?) contains aborted as well as perfect spores, the aborted ones adhering irregu- larly to one another or to the perfect spores. ~ A larger or smaller number than 8 is the typical number of spores in the asci of some Ascomycetes; 1-2 for example in Umbilicaria and Megalospora, Mass.; 2 in Erysiphe guttata, Pertusaria sp. and Endocarpon pusillum; 4 in Erysiphe sp. and in Aglaospora profusa; 16 in Ascobolus sexdecimsporus, Crouan*, Hypocrea rufa, P., H. gelatinosa, Tode, H. citrina, Tode, H. lenta, Tode, &c.*; 40, 50 and more in Diatrype quercina and D. verrucaeformis, Calosphaeria verrucosa, Tul., Tympanis conspersa, Fr., and T. saligna, Tode; the genera Bactrospora, Acarospora, and Sar- cogyne of Massalongo have over 100 spores, most species of the genus Sordaria ‘ have 8—spored asci, but in some the asci have 4, or 16-64, or even 128 spores. In some species again the number varies; the asci of Dothidea Sambuci, Fr. produce 2-4 spores, those of Erysiphe sp. and Pertusaria sp. 4-6, Sordaria fimiseda 4-8, S. pleiospora 16-64, and others might be mentioned; in Tuber the number of spores varies as much as from 1-6, and in Elaphomyces from 1-8. The history of the development of these asci has not been so accurately studied, if we except the asci of the two last genera, as that of the typically 8-spored asci; still all that is known of it and of the spores themselves, especially their simultaneous appearance, agrees with the account which has been given of the 8-spored genera. The genera nearest allied to these often have asci with 8 spores, Erysiphe for example, Diatrype, Aglaospora -and Calosphaeria; and asci with 4 as well as 8 spores occur in some species of Sordaria and in Valsa ambiens, V. salicina and V. nivea, some in the same, some in separate perithecia. Hence it may very well be presumed that the formation 1 Mém. sur les Lichens. See the literature cited at close of section LXXIV. ? Crouan in Ann. d. sc. nat. sér. 4 (1858). 8 See Currey in Trans, Linn. Soc. London, XXII. * G, Winter, Die deutschen Sordarien, Halle, 1873. 80 DIVISION I,-—GENERAL MORPHOLOGY. of spores in these instances differs from that in the 8-spored asci in no other respect than in the number of nuclear divisions and spore-primordia. Whether regular abortion of a certain number of original spore-primordia occurs in individual cases, where the number of perfect spores is small, is still uncertain. The formation of the spores too in Tuber and doubtless also in the rest of the Tuberaceae and in Elaphomyces differs much less from that in asci with 8 spores than appeared from my former observations, which were conducted with imperfect means. There also we find simultaneous orientation of spores and nuclei. The inequality in the number of the spores is due partly to the inequality in the number of the original spore- primordia or divisions of the nucleus, partly to the frequent want of uniformity in later developement and to the partial disappearance of spores after they are once formed. In the full-grown stalked spherical ascus of Tuber (T. aestivum, T. melanosporum, T. brumale (Fig 40) and their allies) the protoplasm which is at first irregularly granular and interspersed with vacuoles becomes differentiated into a dense parietal strongly refringent layer of glycogen, which turns a brownish red with iodine, and an excentric spherical cavity filled with finely granular weakly refringent protoplasm which becomes FIG. 40. Tuber brumale, Vitt. Full-grown asci isolated in water. @ protoplasmic cavity separated from the layer of glycogen. 4 six young spores visible in the protoplasm. c¢ shows one spore half matured and two which have remained quite small in the same position. Magn. 390 times. yellow with iodine. The limiting layer of the glycogen-mass is very compact where it borders on the cavity, and its double contour is often so sharply defined that older writers supposed it to be the membrane of a special cell. The spores are formed in the protoplasm. Observations made by Errera have shown that there is one nucleus in the protoplasm, visible even in younger asci, which by successive divisions gives rise usually:to 4-6 nuclei; then as many spore-primordia appear simultaneously and in close proximity to one another round these nuclei in the form of small and very delicate cells. As the cells now begin to grow they move further apart and usually develope unequally, some outstripping the others, while some remain Stationary at an early stage of development and at length disappear. Hence the frequent occurrence of quite delicate spore-primordia with others that are far advanced, which once led me to suppose that they were formed successively, and hence also the unequal number of ripe spores, varying from 1-4-6 in an ascus. The old drawings reproduced in Fig. 40 will sufficiently illustrate the subject for the present. The asci of Elaphomyces granulatus are of similar form to those of Tuber, and contain before the orientiation of the spores a very transparent protoplasm forming a thin parietal layer round one or more vacuoles and turning yellow with iodine; no glycogen-mass appears in them. I found in the lower third of a half-developed ascus where the great increase in breadth begins, a small but distinct nucleus with the CHAPTER III,—SPORES OF FUNGI. f 81 structure of that in Peziza confluens ; I could not see it in the ascus when fully formed, but the young spore-primordia on the other hand have a distinct nucleus. The spores lie close together and form a small group of usually six small round delicate cells, which occupy the apex or a part of one side of the ascus ; they are all alike when quite young and were probably therefore formed simultaneously, but they develope very unequally ; the mature asci contain from one to eight, usually six spores. c. The formation of spores in the sporangia of Protomyces macrosporus (Fig. 41), if the expression is allowable in this case, takes place after they are laid on or in water. Before the water makes its way into them they have experienced complex changes, which cannot be further described in this place, and have assumed the form of spherical vesicles (Fig. 41 4) the walls of which are lined with a layer of dense granular protoplasm (c) enclosing a large central cavity filled with water. No nuclei have been seen in them. The layer of protoplasm now breaks up simultaneously all round the cell usually into hundreds of ‘spores’ (d), which when the separation is complete are small polygonal finely granular bodies parted by narrow hyaline streaks, FiG. 41. Protomyces macrosporus, Unger. a mature resting-spore in the dormant state (see section LIII) with the remains of the hypha on which it was formed. 4 further development when cultivated in water; the protoplasm enclosed in an inner layer of the membrane (inner cell) swells up and escapes from the ruptured outer layers of the membrane. c—e development of the spores in the inner cell (sporangium) which has escaped from the outer cell. In c the protoplasm is parietal. In @ the protoplasm is divided into spores. In ¢ the spores form a cluster and are separated from the layer of protoplasm which still lines the wall. Magn, 390 times. and presently assume the form of small cylindrical rods about 2. 2 yw in length. The differentiation in the protoplasm described in my work quoted in section LIII as preceding the partition requires fresh examination. A granular parietal layer of protoplasm which permanently clothes the membrane and a small portion of hyaline substance between the spores, possibly of the nature of. protoplasm, is not employed in the formation of the spores. The latter substance becomes visible, when the spores — have taken the form of rods and have collected into a ball (e) on one side of the wall of the sporangium, as a series of radiating threads running from the ball of spores to the wall-utricle; but by degrees it disappears entirely and a watery fluid takes its place. Section XX. The spores which are produced endogenously are usually set free from their mother-cells in some determinate manner as soon as they are ripe and fully grown. In a few cases, as in Elaphomyces, Eurotium and. perhaps in Penicillium, they escape from the mother-cell before they have acquired the size and structure which usually precede germination, and they subsequently attain to these at the expense of dissimilar cells which had surrounded the sporangium. In extremely rare [4] : G 82 DIVISION I.—GENERAL MORPHOLOGY. and exceptional cases the release of the ripe spores is left to chance, there being no special arrangement made for it, and the spores may even germinate inside the mother- cell, the germ-tubes piercing or bursting through its wall, as may be seen in the sporangioles of Thamnidium and its allies. The arrangements for the escape of the spores vary in different species. a. The aquatic swarm-spores of the Saprolegnieae (with one partial exception to be noticed hereafter), of the Peronosporeae and Chytridieae make their exit through a narrow orifice, formed usually at the apex of the wall of the mother-cell by the sudden swelling and disappearance of a circumscribed portion of the wall of the mature sporangium. The spot is marked out in many species by gelatinous thickening of the membrane before it begins to swell. This is nowhere more conspicuous than in the sporangia of Phytophthora, in some species of Peronospora, and in some of the Chytridieae which have gelatinously thickened terminal papillae; in other cases, as Saprolegnia, the thickening has not been observed. While the place of exit swells, the entire contents of the sporangium, the mass of spores and the surrounding matter, absorb water and also swell’; and as the lateral walls of the sporangium are but slightly extensible, the spores which lie beneath the place of exit are first squeezed out through it and the others follow. The proceeding may vary in individual o = “i za cases, and it remains for investigation aL to determine to what extent the spores @ themselves, the intermediate parting @ substance (see p. 74) and perhaps also an inner layer of the wall of the spor- ; angium, participate in the first general ws fen, Lteniiora injeians Mest. asperangim vingin swelling caused by the absorption of spores from the sporangium. spores in motion. dthesamecome water, In the cases which have ‘been to rest and beginning to germinate. Magn. 390 times. more carefully examined (Achlya, Sap- rolegnia and Phytophthora, Fig. 42) it can be seen directly that it is the hyaline substance surrounding the spores inside the firm wall which swells the most. Itis also observed in most cases that a hyaline layer on the inner surface of the firm wall first comes into prominence, and increases in breadth and pushes the mass of spores towards the middle of the sporangium and the place of exit. ‘The spores, even where as in some cases they show independent movements before they are set at liberty, are now virtually passive, and in Achlya especially they are evidently squeezed together as they escape from the sporangium by the limpid mass which surrounds them. It is therefore in the swelling of this mass that the expelling force resides ; but it is still uncertain whether the mass consists entirely of the original soft partition-layers which must in that case suffer partial dislocation when the spores are discharged, or whether an innermost layer of the wall of the sporangium swells and some product from the spores themselves is also added. The phenomena connected with this swelling at the place of exit occur only at a given moment after the formation of the spores is completed, and in water more- over which is perfectly pure and contains free oxygen. That the point of exit, which 1 Walz, Bot. Ztg. 1870, p. 689. CHAPTER III.—SPORES OF FUNGI. 83 has in many cases been formed some time before and gelatinously thickened, does not swell in the water before this moment must be due to its not having yet undergone the change which takes place in it after the spores are matured, supposing both phenomena to have a common cause or the cause of the change to lie in the ripe spores. In the latter which is the more probable case we are almost compelled to suppose that some secretion must proceed from the spores, which acts as a ferment altering and dissolving definite portions of the wall which had been previously prepared. The same view will apply with slight modification to the substance inside the persistent firm wall of the sporangium which is capable of swelling and takes an active part in the expulsion of the spores, and to the discharge of the zoospores of many of the Algae. On the special features in the formation of the zoospores of Pythium, the formation of small heads in Achlya, Aphanomyces and Achlyogeton, and the coating of the spores in these genera and in Dictyuchus, which cannot be further described in this place, see section XL and the special literature there cited. b. The upper and largest portion of the outer wall of the spherical sporangia of Mucor (including Thamnidium, Rhizopus, Absidia, Phycomyces, &c) and Mortierella is changed when the spores.are ripe into a substance which dissolves in water, and in most of the mucor-forms is incrusted with a thin spiky coating of calcium oxalate. The presence of the smallest quantity of water causes the wall and the substance between the spores which is present in greater or less abundance to dissolve and liberate the spores (see p. 75). The lower portion of the outer wall which surrounds the point of insertion does not participate in these changes and remains after the dissolution of the rest of the sporangium as a ring or collar round its insertion; the basal wall is also persistent and forms in Mucor the strongly convex or even vesicular structure known as the columella. In the allied genus Pilobolus the sporangium has at first the shape and structure and even the oxalate incrustation of that of Mucor. The upper and larger portion of its outer wall is very firm and of a bluish black colour; a comparatively narrow annular zone round the point of insertion is more delicate and colourless. The mass of spores contained in the sporangium is at first surrounded, especially at the point of insertion of the sporangium, by a colourless gelatinous layer lying between the spores and the wall, and endowed with great capacity for swelling in water. This layer appears to be developed to a greater or less extent according to species, but whether it is originally a part of the wall of the sporangium or formed like the spores from the contents of the sporangium is at present uncertain. If water reaches the thin basal zone of the outer wall it penetrates through it and causes the gelatinous layer which lines it to swell up at once, and the wall of the sporangium is consequently ruptured round the point of insertion and carried upwards by the continuously swelling substance. It is not known whether the membrane is still intact when the water makes its way through it, or whether fissures for the admission of the water are previously formed in it as the result of changes of form and varying moisture after maturity: In species like Pilobolus anomalus, Ces. (Pilaira, v. Tiegh.) with very long filiform sporangiophores, nothing further happens beyond the gradual solution of the gelatinous layer and the breaking up of the mass of spores; but in most species (P. crystallinus, P. oedipus, &c.) the ripe sporangium is abjected from G 2 84 DIVISION I,-—GENERAL MORPHOLOGY. its sporangiophore and adheres by means of the gelatinous layer to foreign bodies, while the spores swell to their full extent and are disseminated. ‘The sporangio- phore in these species’ is a cell some millimetres in length, cylindrical in its middle portion, but inflated in its lower part and in its upper part especially just beneath the sporangium. It becomes more and more turgescent after the spores have matured and causes abjection of the sporangium by means of the mechanism described on page 72. The separation takes place in the line of an annular fissure, which is close beneath the insertion of the outer wall of the sporangium and is seen before the sporangium is flung off as a fine sharply marked line on the wall (Fig. 38). The delicate wall of the lower portion of the sporangium is ruptured at the moment of abjection, being struck by the ejected fluid, and thus the swelling of the gelatinous layer investing the spores is secured. The sporangium is sometimes abjected with considerable force. The sporangia of Pilobolus oedipus, in which species, according to Coemans and Brefeld, the greatest amount of force is exerted, are thrown, as we learn from the former authority, to a height of more than 1.05 M. The process, as Coemans has also proved, is greatly ‘dependent on the amount of light. Under favourable circumstances the development of the sporangiophore begins at midday or in the afternoon ; it is completed and the sporangia and ‘spores are also formed during the night, and the sporangium is thrown off during the following morning at dn earlier or later hour according to the greater or less amount of light. Exclusion of light does not entirely prevent abjection but may delay it 12-15 hours. P. oedipus shows this sensitiveness to light and the normal periodicity to a less extent than P. crystallinus. We must not enter further in this place into the connection between these phenomena and the very strong positive heliotropism of the sporangiophore. The increasing turgescence of the sporangiferous cell before abjection, assuming that the superficial extent and elasticity of the membrane remain the same, may be caused either by increasing osmotic absorption of water on the part of the sporangiferous _ cell itself, or by the forcing of water from the mycelium into the passive sporangiferous cell, or by the combined operation of both these agencies. In my first edition I assumed that the latter of the two was the only operative cause, because a drop of water which increases in size is often seen to issue after abjection from the open sporangiferous cell before it finally collapses. More exact measurements are required for the confirmation of this view. Section XXI. The spores produced in asci and those of Protomyces macrosporus are set free in one of two ways according to the species; either by ejection ® (Ausschleuderung, Ejaculation) or by solution or gelatinous swelling (Auflésung, gallertige Verquellung) of the asci. The first process, the process of ejection, is found only in the case of spores which normally attain their full development inside the ascus. As they advance towards this state, the protoplasm around them and the glycogen-mass subsequently formed constantly diminish in quantity, being doubtless used to a great extent as material for the formation of the spores. We are not at present in possession of more 1 Coemans in Mém. conc. de l’Acad. royale de Belgique, XXX.—J. Klein in Pringsheim’s Jahrb. VIII, p. 305.—Brefeld, Schimmelpilze, I and IV.— Van Tieghem, Mucorinées. See also the literature cited in sections XLI-XLIV. 2 ‘Abjection’ and ‘ ejection’ have been adopted as renderings of ‘Abschleuderung’ and ‘ Ausschleu- derung,’ the throwing off or throwing out with force of spores from the sporogenous structure. CHAPTER III,—SPORES OF FUNGI. Ae 85 exact knowledge on this point. When the spores are ripe a considerable quantity of protoplasm richly interspersed with vacuoles still remains in some species, as Sphaeria Lemaneae’, S. Scirpi and Sordaria fimiseda; in most cases, however, the residue is but scanty, but in all without exception the inner surface of the membrane is covered by an unbroken though often very thin layer of protoplasm. ‘The chief portion of the contents of the ascus surrounding the spores consists of an apparently watery fluid. The membrane, which when young is always delicate and not stratified, increases in thickness as the ascus matures, but often shows no signs of being divided into layers even in such large asci as those of Morchella esculenta, Peziza Acetabulum, P, pitya, P. melaena, and Ascobolus furfuraceus ; in some species, especially in Lichen- fungi, it is distinctly stratified, and in a number of cases, which will be noticed more fully below, it has peculiar local thickenings at the apical extremity. It shows the reaction of Fungus-cellulose in most Fungi; yet a dilute solution of iodine producesa blue colour in not a few cases, either over the whole of the ascus, as in most Lichens and in Peziza convexula, P. cupularis and others’, according to Coemans in some species of Ascobolus also, or only at the apex of the ascus, as in some instances which will be considered at greater length in the sequel. The ejection of the spores from the asci is either s¢mulfaneous or successive. The simultaneous ejection of spores is much the most common, occurring in nearly all the Discomycetes, in the Erysipheae, in some Sphaeriaceae and in the sporan- gia of Protomyces. Certain special modifications are said to occur in Lichen-fungi and will be noticed again further on; but except in these cases the ejection of the spores is due to the same mechanical arrangement as that which causes the abjection of the spores and sporangia of Empusa or Pilobolus. It has been carefully observed (with the exception of the case of Protomyces which must be at present disregarded) in club- shaped or ovoid asci which are broader towards their free extremity and contain four, eight, sixteen, or more rarely a larger number of spores, After the spores are matured the ascus with its parietal layer of protoplasm enclosing a constantly augmenting quantity of watery fluid expands considerably and becomes more turgid. The expansion may amount to five-fourths or four-thirds or even to twice or several times the original diameter of the ascus, i.e. the diameter at the time of the ripening of the spores, and takes place in the direction of the length as well as the breadth, affecting especially the upper and apical portion of the ascus. That the membrane of the ascus is almost entirely passive in this extension and continues to be perfectly elastic may be proved at any time by cutting it through or by extracting the water. When the ascus begins to expand the spores move into its apical region, where they are closely packed together in the watery fluid and in the simplest and most common case are arranged in a single longitudinal row, the uppermost member of which is close beneath the apex; it is more unusual for them to form two or more _ irregular rows, as in Ascobolus and its allies. In some cases gelatinous appendages which will be described by-and-bye, serve apparently to keep the spores in their relative positions in this arrangement or at least to assist in doing so*. According to 1 Woronin, Beitr. III. * See also Nylander in Flora, 1865, p. 467. * Zopf in Sitzgsber. d. Berliner naturf. Freunde, Feb. 17, 1880. Zopf’s last work on this subject (Zeitschr. f. Naturaw. 56, Halle, 1884) could not be consulted. ~ 86 DIVISION I.—GENERAL MORPHOLOGY. Zopf the uppermost spore in some Sordarieae is even attached to an inwardly directed process from the membrane at the apex of the ascus. No such arrangements have been observed in the majority of cases, and the apical position of the spores is sufficiently explained by the consideration that the one-sided expansion of the apical region must produce currents in the contained fluid in the direction of the apex, which must push the spores suspended in it towards this expanding apex. When the wall has reached a fixed maximum of extension, it suddenly gives way at a point of least cohesion near the apex, which is the pocnt of dehiscence; at the same moment the elastic lateral wall contracts to the size spoken of above as the original size, and the apical portion of the fluid contents together with the group of spores is driven out through the fissure. Then the open ascus collapses and perishes. The arrangement of the spores in the apical portion of the ascus before their ejection, when there are no special arrangements for attaching and securing them, is evidently the result of the conditions of space and form. In many Discomycetes for instance the spores are ellipsoidal or elongated, and their length greater than the breadth of the ascus ; they lie therefore parallel in the ascus, in a single longitudinal row close behind one another, each placed obliquely and touching the wall of the ascus with both ends, the uppermost one having its upper extremity close to the apex (Figs. 39 w and 43). Ifthe breadth of the ascus is much greater than the diameter of the spores the arrangement is more irregular; thus there is an irregular longitudinal row in Ascobolus pulcherrimus?, two such rows in many Ascoboli? (Fig. 45), and an irregular ball crowded up into the apex of the ascus in the eight-spored asci of Exoascus Pruni*® and in the many-spored asci of Ryparobius*. But the longitudinal arrangement is maintained in the comparatively very broad asci of Sordaria (Fig. 44), where it may be due to the attachment of the spores to one another. The form of the fissure varies with the species, and it cannot always be distin- guished with certainty. A longtitudinal rent simple or lobed, passing over the apex and leaving a broad hole when the ascus is emptied, forms the opening in the asci of Exoascus Pruni, Peziza cupularis and Erysiphe®, and according to Boudier * of Geoglossum, Helotium, Leotia, and Bulgaria sarcoides. In many Pezizas, as P. convexula, P. confluens, P. granulata, P. abietina, P. vesiculosa, P. melaena, all the Ascoboli and Helvella crispa, the fissure is annular and runs close beneath the blunt summit of the wall of the ascus, which is therefore cut off like a lid, and when the spores are ejected is lifted off either all the way round or only on one side where the uppermost spore touches the wall of the ascus; the latter is the case, for instance, in Peziza vesiculosa and P. granulata. In larger Ascoboli the edge of the lid may be seen before the ejection of the spores as a distinctly marked transverse line’. In some forms, as P. abietina and P. vesiculosa, 1 Woronin, Beitr. II, t. III. 2 Boudier in Ann. d. sc. nat. sér. 5, X. ® De Bary, Beitr. I, t. III. * Boudier, l. c. 5 R. Wolff, Erysiphe ; see the literature cited in section LX XIV. 6 Loc. cit. p. 202. 7 See Boudier’s figures, 1. c. CHAPTER III,—SPORES OF FUNGI. 87 it is the apical and most extensible portion of the wall and chiefly the area forming the lid in that portion which is most distinctly coloured blue with iodine. In the Sordarieae also I frequently saw the ascus open by a comparatively tall lid. There is a third series of cases in which the spores are ejected through an apical perfectly circular hole which before ejection of the spores is a circumscribed thinner or less compact portion of the wall of the ascus. In Rhytisma acerinum this hole is replaced by a minute mucro forming the uppermost extremity of the apex of the still closed ascus. In Peziza Sclerotiorum (Fig. 43), P. tuberosa, and their allies, the wall of the ripe but not turgescent ascus is more than twice as thick at the slightly convex apex before the spores are discharged than it is on the sides; it is also formed of two layers and is traversed in the middle by a longitudinal streak which is less strongly refringent and looks like a stopper inserted in the ascus. The apex of the turgescent ascus, ready for the ejection of its spores, is considerably broader and strongly convex outwards, with its wall not thicker than the lateral walls and with none of the in- ternal structure just described. The spores are discharged through the stopper, and after the discharge there is an open passage in its place round which the form and structure of the non-turgescent state are once more restored. In these cases again the apical portion of the wall, which is most capable of stretching and is thickened when it is not in a state of tension, is that which turns blue with dilute solution of iodine, and the stopper which indicates the point of dehiscence is most intensely coloured. The following remarks will further illustrate the above short account of the mechanism for the ejection of the spores. a. The expansion of the ascus by increase inthe amount Fic. 43, Pesiza (Sclerotinia) Sclero- +4 ‘ cy tiorum. Asci observed as they lay of its fluid contents has been directly observed. That (ory ee oer ature -ascus this is merely a passive stretching of the cell wall, and before ejection of the spores. 6 the ° a same after ejection. c¢ another specimen not a phenomenon of growth with permanent results, is in the same stage of development as a, shown by facts which are easily observed, namely, that “it {wou “ansversely., Magn. about the ascus contracts to its previous dimensions after dis- charging its spores, or if an artificial opening is made in its wall while its membrane at the:same time increases in thickness, as is shown most clearly in the case of the strong local thickenings which have been described as occurring in Peziza Sclerotiorum. This species shows with peculiar distinctness that it is the apical region of the ascus which stretches most; but in all other cases attentive comparison will show that it is the apical region, or pretty well the apical half, which is most altered in form and size while the lower half is little or not at all affected. The directions of greatest extensibility and the shapes produced by them vary much in different species, as appears from a comparison of Figs. 43,44. and 45. The enormous increase in volume of the asci of Sordaria may perhaps suggest actual growth, especially as they are comparatively rich in protoplasm after the spores are matured ; the point requires further investigation, but it should be noticed that the contraction after the ejection of the spores is in this case also very considerable. That it is the increase in the amount of fluid content which causes the expansion 88° ‘DIVISION I,—GENERAL MORPHOLOGY. of the ascus is shown by the fact, that the expansion diminishes with a diminution in the amount of fluid in the cell and disappears, either suddenly and entirely, if the wall of the ascus opens spontaneously or is pierced artificially and the fluid escapes, or gradually through the slow operation of alcohol, glycerine, or saline solutions which withdraw water from the uninjured ascus. On the other hand the expansion of the asci (and ejection of the spores) is promoted by placing uninjured asci in water. 4. The great elasticity of the wall of the ascus is sufficiently shown by the facts above enumerated. . c. The spores are in many cases retained according to Zopf in the expanding apex of the ascus by a special apparatus of attachment'. In Sordaria Brefeldii a hollow cylindrical thick-walled process of the membrane, which turns blue with iodine, reaches from the apex into the lumen of the ascus. The spores, like those shown in Fig. 52, are provided with terminal appendages which connect them together in a row; the distal appendage of the uppermost spore attaches the entire row to the process from the wall of the ascus, ‘ sometimes by thrusting itself into its cavity which it fills up, sometimes by closely grasping it. And this apparatus is further completed by another arrangement; the membrane of the ascus over a subterminal zone is capable of great swelling and can lay firm hold on the appendage borne by the chain of spores, as a hand grasps the throat.’ Similar apparatus may perhaps frequently be in use especially in the Pyrenomycetes, as is indicated by the structural features in the apices of asci which will be discussed in section XXVI. Our present knowledge does not allow us to speak with certainty on this point. In many cases, especially in the Discomycetes, there is no such apparatus present, the spores being suspended in the fluid of the ascus. The spores must have nearly the same specific gravity as the fluid; if not, they would change their position as the ascus changes its inclination, which they do not do. Most, if not all, spores produced in asci sink in pure water; the fluid contents of the ascus must therefore be of greater specific gravity than pure water, since it holds in suspension bodies of greater specific gravity than water. If increase in the amount of the fluid contents causes the apical portion of the ascus to stretch more than the other parts, currents must be set up in the fluid in the direction of the apex and continue as long as the expansion continues, and push the spores therefore permanently towards the apex. The arrangement of the spores may then be affected by special directions in the currents which we cannot at present determine, as well as by. the conditions of space noticed above. | d@. The ascus lined with a layer of protoplasm and preparing to eject its spores is in the condition of a cell in a state of constantly increasing turgescence, the characteristics of which may here be presumed to be known?. It is natural therefore to suppose that the increase in the amount of fluid contents is caused by absorption of water by endosmosis, and that this absorption is due to the operation of osmotically active substances, dissolved in the cell-contents, which cannot pass through the layer of protoplasm. All the facts that have been observed agree with this supposition, and especially the circumstance that volume and turgescence can be alternately: diminished and restored in individual asci by careful removal of water by means of a saccharine solution or of glycerine, and by its reintroduction. The opposite view expressed in the first edition of this work was founded on the fact that the proto- plasmic utricle in the asci which were examined was either injured or killed in the process of withdrawing the water, and it has been shown that isolated asci are very liable to suffer in this way. The presence of the substances which are active ~ agents in inducing endosmosis is evidently coincident with the disappearance of the 1 As cited on p. 85. ? Pfeffer, Pflanzenphysiologie, I, p. 50.—De Vries, Mechan. Ursachen d. Zellstreckung, Leipzig, 1877. . EE CHAPTER III,-—SPORES OF FUNGI. , 89 residue of protoplasm or glycogen-mass as the spores mature. I was unable to determine their character more nearly, and can now only state that neither sugar nor any acid reaction was ascertainable in the fluid contents of the asci of Peziza granulata, P. Sclerotiorum, and Ascobolus furfuraceus. é. It is evident from what has now been said that, other conditions being the same, the ejection of the spores must be hastened by a lateral pressure operating on the ascus from without. This may readily be shown by experiment on isolated asci placed in water beneath a cover-glass. In the living Fungi the asci stand very many together in the hymenium usually with paraphyses between them, and there the lateral pressure on the asci increases in part with the advancing growth, as new asci are introduced between the previous ones, and in part with the addition of water ; the hymenia in the Discomycetes which have paraphyses swell considerably in the direction of.their surface and in greater proportion than the tissue of their sporophores. j. All that has been said of the club-shaped asci may be applied in its main points to the spherical sporangia of Protomyces macrosporus, which are formed free in the water. The place of greatest extensibility, towards which the numerous ‘spores’ move, is in accordance with the shape of the sporangia a broad thin section or pit in the wall, in the middle of which the fissure ultimately appears as a gaping slit. Section XXII. It has been already said that the asei of the Discomycetes of which we now proceed to speak, are arranged-in superficial hymenia nearly vertically to the surface and between numerous paraphyses of uniform height, the extremities of which indicate the middle level of the hymenial surface. The asci of a hymenium are not developed simultaneously; during a period of time which varies in different species new asci grow up one after another from beneath between the paraphyses, while the older ones are ripening. When the asci approach maturity and begin to enlarge each one elongates so much that its apex projects above the surface of the hymenium, while its basal portion continues attached to the original place of insertion. After ejection of the spores the ascus shrinks and the apex usually returns to below the level of the hymenial surface. Where there are no paraphyses, as in Exoascus, the same phenomena are observed with the modifications which that difference naturally entails. _ In the hymenia of Peziza, Helvella, Morchella, Bulgaria, Exoascus, and the ma- jority of the Discomycetes when they are ripening, the individual asci are constantly discharging their spores in succession. If the Fungus is placed in a closed and damp chamber and a glass plate is set in front of the hymenium, spores are soon found lying usually eight together in a minute drop of fluid, and gradually the plate becomes thickly strewed with them. But besides this gradual emptying of the asci many of the Dis- comycetes have the peculiar habit of ‘ puffing’ (Stauben), that is, of suddenly discharging a whole cloud of spores, if they are shaken, or if the chamber in which they have been -kept is opened. The phenomenon is of course produced by the simultaneous emptying of a number of asci. The Fungi on which my experiments were - chiefly made—Peziza Acetabulum, P. Sclerotiorum, and Helvella crispa—do not puff when they are cultivated in a very damp and still atmosphere enclosed by a bell- glass; under these conditions only the continued gradual discharge of the spores takes place. As long as the Fungus remains shut up in the damp atmosphere no amount of shaking will cause it to puff, whether it is kept in the dark or in the light of day, or is suddenly brought from the dark into diffuse or direct sun- | light ; but it puffs as soon as it is removed from the damp chamber irtto a dry go DIVISION I.—GENERAL MORPHOLOGY. atmosphere. If the hymenium is only moderately damp, so that the tips of the ripe projecting asci look like a slight rime or a fine down on it, the puffing commences in a few seconds after the bell-glass or other covering is removed. If it has been kept very wet, the hymenium is covered with a thin layer of water and glistens more or less and is of a darker colour than in the moderately moist condition. In such a hymenium the puffing does not take place till the layer of water is evaporated and the slight rime-like appearance is observed ; the puffing is accelerated by whatever accelerates the evaporation. _ From these facts it appears that sudden loss of water is the proximate cause of the puffing. Since puffing occurs instantaneously in hymenia that are not wet, the withdrawal of water as soon as dry air comes in contact with the Fungus cannot produce it by causing a shrinking and contraction of the entire hymenium and a consequent increase of the pressure on the asci from without. All this could not possibly be brought about to any important extent in one or a few seconds of time, and some simple experiments and measurements are sufficient to convince us that the pressure which operates on the asci from without under long-continued desiccation is not at first increased, and eventually decreases to a considerable extent, but that it increases in proportion as the hymenium absorbs water. The loss of water can only therefore cause the puffing by altering the state of tension in each ascus, either by lessening the expansion of the lateral walls and so . increasing the pressure of the fluid contents on the place of dehiscence, or by lessening the power of the place of dehiscence to resist the pressure which remains unaltered. The correctness of this explanation is confirmed by the observation, that ejection takes . place when ripe isolated asci lying in a little water are suddenly exposed to the operation of reagents like alcohol and glycerine which withdraw their water. The above remarks leave little room for doubt that motion and shaking affect the puffing only by hastening the evaporation of the water. A hymenium which has just sent forth a cloud of spores can be induced to repeat the operation several times, if the plant is moved rapidly to and fro, and the less perfectly ripe asci are made to dehisce. But then, and in many cases after the first puffing, a rest of at least some hours is necessary, that a sufficient number of new asci may come to maturity to allow the puffing to be observed. The phenomenon of puffing is absent from some Discomycetes; I have never been able to excite it in Peziza pitya, Morchella esculenta, or Exoascus Pruni; it is readily produced in the majority of species. I have observed it in Peziza melaena, P. tuberosa, P, aurantia, P. cupularis, P. badia, P. confluens, and Rhytisma acerinum, in addition to the species which have been already named. Many other observations have been recorded since the time of Micheli. In Ascobolus and the genera which have been recently separated off from it ejection is never successive but always simultaneous from all the asci that are at any time ripe in the hymenium, and here too we have the phenomenon of puffing. The mechanism of the discharge and the conditions for the puffing are the same as those which have been described in the case of the other Discomycetes ; but they are also dependent on the illumination to an extent which requires to be more closely examined, CHAPTER III,—-SPORES OF FUNGI. ; 91 Section XXIII. The process of ejection in the Pyrenomycetes which discharge their spores simultaneously was first correctly described in Sordaria by Zopf’. Numerous asci placed upright side by side in a thick tuft fill the swollen enlarged basal portion of a flask-shaped receptacle, the perzthectum, which is continued upwards into a more or less elongated neck. In large forms, as S. fimiseda, the neck is more than a millimetre in length but much shorter in the smaller species, and is traversed longitudinally by a very narrow cana/, not so broad as an ascus, which enlarges into a conical form at its inner end above the group ofasci and is open to the air above at the outer end. ‘Till the spores begin to ripen the asci are between narrowly cylindrical and club-shaped, and of the same height as the basal ventral portion of the perithecium. Then they begin to elongate one after another while they grow much broader at the apex. The only direction in which they can elongate is that of the canal of the neck. When the apex of the first ascus reaches the inner end of the canal, it enters it and swelling there to a broadly club-shaped form, and causing a corresponding enlargement of the canal, it continues to lengthen, till its apex is on a level with the outer mouth of the canal or a little above it; then its ejection takes place. Then the next ascus enters into the now empty canal, and so on one after another. The lower extremity of the ascus continues attached to its original point of insertion at the base of the peri- thecium until ejection. The elongation is therefore very considerable ; in the case depicted in Fig. 44, for instance, it is more than six times the length attained by the ascus at the time the spores are ripe, and is at least three times that length beneath the widened upper part. The lower portion seems to become narrowed at the same time under the pressure of the neighbouring asci which are ae FIG. 44. Sordaria minuta, Fuckel (2). beginning to swell, but it is difficult to be quite certain On Form with 4-spored asci; small perithe- cium grown on a microscopic slide and this point on-account of the strong lateral pressing to- observed in the living state lying in the culture-fluid, in optical longitudinal sec- gether of the parts. tion; at the base of the perithecium is a dense group of asci, most of them with The rapidity with which the elongations are accom- tive spores; above this group are other mature asci in various stages of elongation plished is comparatively small. In a small specimen mas tractor pm Pyne er observed in water the movement of the apex about a neck. Magn. about 100 times. spore’s length (= 17 ») occupied some 15 minutes, and the passage through the whole neck about 8 hours. In the specimen of Sordaria minuta (?) given in Fig. 44 the motion was quicker, a spore’s length of 10 » requiring some five minutes. How far light, heat and other external causes accelerate or retard the movement, and what are the specific differences which certainly exist, are points which have yet to be investigated. Srction XXIV. The force with which the spores are ejected does not appear tobe great. In Bulgaria inquinans and Protomyces macrosporus they are sent straight ? As cited on p. 85. Q2 DIVISION I,--GENERAL MORPHOLOGY, upwards to a height of 1-2 cm., in Exoascus Pruni of 1 cm.; in the strongly puffing Fungi, such as Peziza vesiculosa, P. Acetabulum, Helvella crispa, and Asco- bolus furfuraceus, they are thrown to a distance of more than 7 cm., in Sordaria fimiseda, according to Woronin, they travel 15 cm., in the smaller species of this genus about 2 cm., in Rhytisma acerinum only a few millimetres. The movements in the act of puffing in large hymenia were said by Desmazieres to produce an audible sound, but this has been doubted by recent observers ; I have myself however heard a very perceptible hissing noise produced by strong specimens of Peziza Acetabulum and Helvella crispa. ‘ The peculiar features in the old genus Ascobolus (including Saccobolus and others), which led to many false and even strange notions, are connected with the large size of the asci, the great prominence above the surface of the hymenium at the period. of maturity, and the regular periodicity in their ripening and in puffing’. Coemans has given us a full account of how a number of asci ripen and eject their spores daily for several days together, when the hymenium has reached a certain point of development. The asci in consequence of their expansion begin to appear above the surface of the hymenium towards evening and continue to do so till the succeeding afternoon; between 1 and 3 o’clock the tension reaches its highest point, and the slighest shock causes ejection which is simultaneous in all the projecting asci. It is difficult to determine whether ejection takes place when everything around is perfectly still. The still- ness is in fact always broken by a number of younger asci beginning to expand every afternoon in preparation for ejection on the following day. It is natural to suppose that there must be a direct relation between this regular daily periodicity and the light-period, and Coemans found that ejection was delayed 4-5 hours in the Ascoboli, when culti- vated in darkness. Boudier and Zopf observed that the asci FIG. 45. mema, show no marginal progressive growth or only a trace of it. In this respect and in some others also their development approaches that of the Pyrenomycetes. FIG. 8&9. Lecauora subfusca. Median section through a young apothecium, swollen up in ammonia, somewhat diag ically rep d; 4% hymenium, ¢ excipulum from which spring the paraphyses represented by strokes run- ning vertically ds h, sh ascog' hyphae giving rise to the asci, » rind, # medullary layer of the thallus which forms a rim round the excipulum, The round bodies are the algal cells contained in the thallus. Magn. 190 times. This is the case in a still higher degree with the ascocarps of the Hysteri- neae and Phacidiaceae, the structure and development of which have been but little examined. According to Hartig’s account of Hypoderma macrosporum and H. nervisequum and my own imperfect observations on some species of Rhytisma and Phacidium, the hymenia in these groups are formed in the interior of flat sclerotioid Fungus-bodies (zy/oma, see p. 43), and become exposed at the time of maturity, when the layer of tissue over the surface of the hymenium separates from it ire FIG. 90. Thelidz tne retells 4 perithecium borne on the thallus;.@ group of Algae, # the part of the thallus in the substratum which has no Algae, 7 the perithecium in median section diagrammatically repre- sented and slightly magnified. 2a group of Algae with hyphae winding round them. After Stahl. Magn. 480 times. and tears asunder in the mode which has often been described in the accounts of the different genera. In this case there are at first only paraphyses present in the hymenia ; the origin of the asci which are introduced between them has yet to be exactly ascertained. Section LXI. “The perithecia of the Pyrenomycetes (Fig. 90, see also Fig. 44), may be described as cup-shaped discomycetous sporocarps with the margin CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES, 1gI incurved so as to form a narrow-mouthed cavity. They are generally roundish or flask-shaped, and they are seldom more, usually less, than 1 mm. in height. They are bounded on the outside by the wa/? which encloses an asciferous hymenium, and are furnished in the full-grown state with a narrow aperture or ostiole (ostiolum, pore), which is a canal passing through the wall and serving for the discharge of the spores (section XXIII). The ostiole usually lies at the apex in reference to the point of origin of the perithecium, seldom at the side (Pleurostoma, Tul.) or at the base (Melanospora parasitica). In many species the orifice is drawn out into a conical or cylindrical ‘neck (tubulus of Tode), through the, middle of which the canal passes, and which in some cases, as in the Valseae, Sordarieae, and Melanospora, may be more than 1 mm. in length. The asci are inside the perithecium on the side away from the ostiole, and are borne on the ascogenous hyphae or cells from which they successively shoot out, as in the Discomycetes. With this mode of formation it is possible for some hundreds of asci to be formed in the small space of some perithecia, new ones continually appearing in place of the ripe ones which have discharged their spores. The asci together either exclusively form the hymenium or are at least its most essential parts; the hymenium either occupies a narrow bit of surface opposite the ostiole of the perithecium, on which the asci grow as a small tuft parallel and erect towards the ostiole, or is spread over a larger, sometimes over the largest portion of the inner surface of the wall, and the asci then converge radially towards the middle line of the .perithecium. Here too the asci and ascogenous organs alone form the ascus-portion of the perithecium; all the other parts belong to the envelope-apparatus; in structure therefore they are on a smaller scale than the envelope-apparatus and in their main features they are like cup-shaped apothecia. | The wail is formed of a dense hyphal weft or pseudo-parenchyma, in Pleospora, according to Bauke, of actual parenchyma-like tissue. It is usually differentiated — into a stronger often sclerosed outer layer, the thickness of which varies in the individual, and which can produce rhizoids. and various other hair-structures on peri- ~ thecia which stand detached on the mycelium, and an inner layer with delicate and often large cells. In some perithecia inserted in stromata, for instance in Tulasne’s Dothidea, in Claviceps, species of Cordyceps and Polystigma, this differentiation does not occur or it is not very distinct, and the wall is formed almost throughout of delicate cells. In its quite young state the wall is entirely closed round the initial.organs of the ascus-apparatus and its ultimate investment, which latter will be described below. The ostiole is not formed till the development is more advanced, and it appears as an intercellular passage in the originally close tissue; it is partly schizogenetic. by the separation of persistent tissue-elements in consequence of unequal growth, partly lysigenetic by the dissolution of a strip of tissue lying originally in the direction of the canal. The two processes seem to be often combined, and it is not easy to decide whether there is a solution of small strips of tissue along with the schizogenetic formation, or not. The ostioles in Sordaria, Melanospora, Claviceps, Epichloé, in Eutypa also according to Fisting’, and Stictosphaeria are very largely schizogenetic; Fiiisting finds the lysigenetic formation Bot. Ztg. 1868, pp. 369, 641. 4 192 DIVISION II,.—COURSE OF DEVELOPMENT OF FUNGI. in Diatrype, Verrucaria, Endocarpon, Pyrenula, and in a very striking manner in Massaria and its nearest allies. In the latter the perithecia are formed inside a flat stroma which lives in the rind of trees, and the orifice is due to the disorgan- isation and ultimate disappearance of a comparatively thick strip of tissue outside and over the apex of the perithecium, together with the tissue of the rind enclosed by it. The neck is of course a prolongation of the wall, chiefly of its outer layers; this appears very distinctly in some perithecia developed in the interior of the thallus, as in Xylaria, the Valseae, Verrucaria, Endocarpon, and species of Pyrenula’, where it pierces through the surface of the thallus and comes out to the air. Its de- velopment is either rapidly completed at an early period, or it is capable under certain conditions of a long-continued apically progressive or intercalary growth in length, and while this is proceeding it is, especially in Sordaria®, in a high degree heliotropic; this variety in the mode of development depends on the species and genus. The ase? are inserted in the places in the delicate tissue of the inner wall which have been already indicated, and the ascogenous hyphae or cells are thrust in between the elements of the wall or lie immediately upon them, The asci fill the inner space of the perithecium, or at least the largest part of it, excepting the neck. All the space not occupied by them is filled with branches of the hyphae, which grow out from the inner layer of the wall toward the median line of the perithecium. Some of these branches lie between the asci, and are then termed paraphyses, as in the Discomycetes, and stand in the same relation as regards their development to the asci as in the Discomycetes, since as parts of the envelope they are formed before the asci which are afterwards introduced between them. Others may cover the portion of the perithecium which is without asci, and even the canal, and then they are called by Fiiisting perzphyses, In the canal they are like small closely set hairs of uniform height, which converge from all sides and are directed obliquely upwards towards the median line of the canal where their extremities almost touch. Below the inner (lower) entrance of the canal, in the part of the perithecial cavity where there is no hymenium, their direction and arrange- ment either remain the same as in the canal, as in Chaetomium and Sordaria fimiseda, or they point downwards towards the median line and the hymenium (Fig. 90). . Periphyses would appear to be seldom entirely wanting, though this is sometimes the case, according to Fiiisting, as in some species of Massaria. It more frequently happens that there are no paraphyses between the asci, and then the asci alone constitute the hymenium; this is the case in Sordaria, Melanospora, Claviceps, Epichloé, Chaetomium (Zopf), Sphaeromphale, and species of Dermatocarpon, Endocarpon, and Verrucariae (Winter, Fiiisting), Further details will be found in special treatises, though the accounts there given must often be received with caution, for the paraphyses and periphyses and other organs are often delicate and perishable, or easily overlooked or confounded if the observations are not conducted with sufficient care, and thus mistakes may often be made, especially if the material is not in a favourable state and the observer is wanting in experience, > Bot. Ztg. 1868, p. 641. 2 Woronin, Beitr. II, CHAP, V.—COMPARATIVE REVIEW.—ASCOMYCETES.—ELAPHOMYCES. 193 It has already been said that the wall or outer wall of the perithecium is usually thick, and often firm and hard. That which is enclosed by it is on the contrary comparatively soft, and has usually great capacity for swelling in water; it comes. out from the firm wall, when a perithecium is opened, like a soft kernel from its shell. Hence the old expression Aernel or nucleus of the perithecium, which included all the soft parts described above, the asci first of all, and then the paraphyses, periphyses, hypothecium, and the soft layers of the wall; it had therefore no strict morphological foundation. Section LXII. The cleistocarps of the Cleistocarpous Ascomycetes are, as their name imports, surrounded by a wall, which remains closed and without an ostiole even when the spores are ripe, and the latter are only released by external influences which cause the rupture of the wall or by its decay. A great variety of special forms are included under these general characters. A number of these are in other respects scarcely anything else than simple pyrenomycetous perithecia without an ostiole. Among the Chaetomieae which have been carefully studied by Zopf there is one species, Chaetomium fimeti, which is distinguished from all the species nearest to it by this want of an ostiole. Others are removed from typical perithecia by further peculiarities of structure, the Erysipheae, for instance, Eurotium and Penicillium, which can only be briefly noticed here, as they will have to be described at greater length in a subsequent page. The sporocarps also of Sphaerophoron may be mentioned in this connection; their structure is given in Tulasne’, but their development has yet to be ascertained. All these sporocarps may be regarded as perithecia with a greater or less amount of deviation or simplification. The structure, on the other hand, of the compound sporophores of Elaphomyces, the Tuberaceae, Onygena, and Myriangium is quite different. The early stages of their development are still too little known, and we can count them among the sporocarps of the Ascomycetes only because they form asci and on the ground of some other analogies and resemblances; whether they can rightly be regarded as homologous with the others must for the present be left undecided. With this reservation a short description of these forms may be inserted in this place, as it will be scarcely possible to recur to them while subsequently relating the histories of development. 1. Elaphomyces. The sporocarps, which become of the size of a hazel-nut as they ripen, are round hollow bodies with a perfectly closed wall, usually known as the peridium, and enclosing the sporiferous tissue or g/eba. The wall is some millimetres in thickness and consists of two firmly connected concentric layers. The inner of the two, the peridium in Vittadini’s narrower sense, is a dense and massive tissue of hyphae which are sometimes very thick-walled. The outer layer, the cortex of Vittadini, is thinner and of a consistence which varies with the species, and may be smooth, warted, hairy, or spiky. Its structure also varies with the species, and in most of them has not yet been described with exactness. In Elaphomyces granulatus it is hard and brittle and thickly beset with warts; the centre of each wart is formed of a conical group of irregularly shaped cells with their bright yellow walls everywhere strongly thickened. The bases of these cones are immediately on the inner layer, and touch each other by their sides. The intervals between the cones and the summits are occupied by a tissue without interstices composed of many layers concentric to .) See the figures in his Mém. sur les Lichens. [4] (a) 194 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. the surface of four-sided prismatic cells; the cells in each layer are arranged in rows which radiate from each cone and meet those which proceed in the same manner from the neighbouring cones. A section parallel to the surface is consequently made up of delicate roundish facets composed of radiating rows of cells, each of which has in its centre a group of thick-walled bright yellow cells. A loosely felted weft of slender hyphae with elongated segments proceeds on all sides from the inner surface of the peridium and traverses the gleba; here and there, especially in younger specimens, the hyphae are more closely combined into larger plates or strands, but there are no distinctly closed chambers. The gaps in the weft of slender filaments are everywhere loosely filled with ascogenous hyphae twice or thrice the thickness of the other hyphae, which are divided into short cells and are often coiled into knots and bear asci on the extremities of their branches. As the spores ripen the whole of the ascogenous tissue becomes mucilaginous and disappears, while the tissue with the slender filaments remains behind as the delicate ‘capillitium’ between dry masses of spore-dust. On the asci and on the ripening of the spores, see above, pp. 80 and 97, The spores are’ large and globular and remarkable for the enormous thickness of their walls, which may be more than two-thirds of the semidiameter of the spore; the wall consists chiefly of a thick, gelatinous, stratified, colourless membrane, covered on the outside with a thin but firm and darkly coloured episporium. For further details see Tulasne’s Fungi hypogaei and De Bary’s Frucht- entwicklung der Ascomyceten. The germination of the spores has not been observed. A few observations only have been made on the early stages of the development of Elaphomyces. The youngest sporocarps of E. granulatus which have come under my notice are small round bodies from 14 to 2 mm. in size in the interior of a compact dirty- yellow filamentous mycelium. Their outside is covered by a cortical layer of the same thickness, colour, and warty surface as in full-grown specimens, and consists of a thin-walled pseudo-parenchyma, the elements of which are often in continuous connection with the mycelial hyphae. The cortical layer encloses a tissue-mass of delicate closely woven hyphae, which fills the whole of the interior and shows the same structure, but is differently coloured in different parts ; a small central portion is of a whitish colour, and is surrounded by a dirty-violet layer, between which and the cortex is a narrow white zone. Later states show that the whitish central mass becomes the gleba, the rest the peridium. This structure and the relative size of the separate portions continue unchanged till the sporocarp has reached the size of a large pea. Larger specimens show the gleba proportionately more enlarged than the peridium, and the ascogenous hyphae beginning to be developed between the slender filaments of its original tissue; soon after the gleba forms the chief mass of the sporocarp, which grows by degrees to the size of a hazel-nut. While the peridium consequently increases greatly in circumference, its absolute thickness increases at the same time or does not diminish. The structure of the inner layer and especially the thickness. of its hyphae remain all this time unchanged ; the cells also of the cortical layer become only about one half larger than in the first, observed stage, while the warts multiply so that without altering much in size they always closely cover the surface of the sporocarp, their multiplication being effected by the splitting of one wart into two or more. All this shows that growth must take place up to late stages in the development by simultaneous and continued formation of new cells in all parts. Tulasne’s figures agree with the above account, except in the statement that young specimens must at first be hollow; the difference arises perhaps from variations in the species examined. All the facts seem to show that we have in Elaphomyces a sporocarp with an extremely thick envelope-apparatus and formed of all the described parts except the ascogenous hyphae. The whole recalls the sporocarp of Penicillium, as will be seen from the description of that genus below. 2. The sporocarps of the Tuberaceae have the forms of tubers, which either have CHAP, V.—COMPARATIVE REVIEW,.—ASCOMYCETES.~--TUBERACEAE, 195 an evident basal portion resting on the mycelium, as in Terfezia and Delastria, or are entirely enveloped when young in the mycelium and are connected with it, as in Tuber, the mycelium disappearing when the sporocarp is mature and leaving it naked and detached in the soil. Its surface, if we disregard the frequently occurring warts and roughnesses, is either smooth and marked only with quite irregular and so to speak accidental large unevennesses, as in Tuber aestivum, T.melanosporum, &c. and in Terfezia, or it shows typical pit-like depressions or narrow deep sinuous furrows, as in Hydnobolites and Genabea. The sporocarp in its simplest form, as in Hydnobolites, consists of a fleshy tissue formed of closely woven hyphae, in which numerous asci on the extremities of the branches are everywhere imbedded ; the outermost layer of tissue only forms a kind of wall or peridium, a delicate down composed of sterile hyphae. In a second series of forms we can distinguish between a sterile fundamental mass and a large number of groups or nests of fertile tissue, i.e. tissue containing asci im- bedded in it. The fertile tissue is a more or less compact hyphal tissue in which asci springing from the ends of the branches are distributed irregularly and in large numbers. This tissue fills the spaces between the fertile groups in. the form of. broad bands constituting much the larger part of the sporocarp, as in Genabea, or comparatively narrow plates which show in section as veins with many fine rami- fications, as in Terfezia and Delastria. The sporocarp is surrounded on the outside by a layer of sterile tissue of varying thickness, forming a peridium from which the veins and bands in the interior take their rise; the hyphae of the fertile groups originate in the adjacent sterile hyphae. A third type is represented by the genus Balsamia. The outside of the compound sporophore is a thick perfectly closed peridium, and the interior is divided by means of thick plates of tissue springing from the peridium into many narrowly sinuous air- conducting chambers. The wall of each chamber is covered with a hymenial layer the elements of which are placed at about a right angle to the wall. A similar structure is found in the genus Tuber, or at least in several species of that genus in the young state (T. rufum, T. mesentericum, T. excavatum, &c."), only the chambers are very narrow and very much coiled and branched. But nevertheless hyphae from the adjacent tissue grow into the cavity of the chambers: at an early stage in the development, and fill it quite full with a dense tissue which contains air in its interstices and is therefore white. At the same time the hymenial layer on the walls ofthe chambers increases considerably in thickness, and assumes the character of a massive irregular tissue which everywhere bears asci. The middle layer of the wall of the chamber retains its original condition in some species. It is these relation- ships which produce the characteristic marbled appearance of a section through a ripe or ripening truffle (Fig. 91), in which two kinds of branched veins run through a dark-coloured fundamental mass, the fertile tissue; the one kind dark-coloured and therefore less striking to the sight, which answer to the walls of the chambers and contain no air (venae lymphaticae, veines aquiféres of Tulasne, venae internae of Vittadini), the other whité and conveying air (veines aériftres, venae externae). The former always originate in the inner surface of the peridium. The latter and probably the previous cavities, which they are formed to fill, extend at certain points to the outer surface of the peridium, and form a kind of opening there to the outside ; this takes place either at spots irregularly distributed over the surface, or in such a way that the veins from all parts unite into a chief trunk with an orifice at a fixed spot in the circumference. In some species of Tuber, T. dryophilum, for instance, and T. rapaeodorum, air-veins only can be distinguished in the fundamental mass, which is traversed uniformly in all parts by asci; this is the case at least in all the states of development in which they are at present known. ' Tulasne, Fungi hypog. tt. X VII, XVIII. 0 2 196 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI. With respect to the more minute anatomical structure of the Tuberaceae, it may be further added, that the peripheral layer, known as the peridium, is usually a stout, thick mass of pseudo-parenchymatous tissue. The outer cell-layers are in most cases furnished with thickened walls corresponding in colour to the surface, which varies in shade from brown to black; in a few cases they are thin-walled and have their surface covered with spreading hairs, as in Tuber rapaeodorum, &c. Except in Stephensia, in which the layers of the peridium are distinctly separated from each other, the outer cell-layers pass gradually into the inner and these in like manner into the sterile veins and bands which spread between the fertile tissue, and which either show the same pseudo-parenchymatous structure as the peridium (Genabea) or, as in most cases, have their hyphae disposed in a course which follows that of the veins. Here too ascogenous hyphae appear in the tissue known as the fertile tissue interwoven with but strictly distinct from other hyphae which may,be termed paraphyses. Moreover it often occurs, both in Tuber and Elaphomyces, that a young ascus is placed on a knee of the hypha which bears it in such a manner that it seems to be borne on two small stalks, some- what as in Eremascus which will be described below. Tulasne has given representations of this phenomenon, and Dr. Errera has recently called my attention to it. It may at FIG. 91. Tuber rufum. asmall specimen divided in halfin reflected light: the white veins 7 contain air, the dark ones v fluid, # the hymenial tissue. 4a thinner section through a young specimen in transmitted light ; lettering as in a, light and dark appearance of the veins reversed. @ magn. 5 times, d 15 times. least be a question whether the development of the ascus in these cases is the same or similar to that of the ascus in Eremascus ; the whole subject requires investigation. The genera Hydnocystis, Hydnotria, and Genea are not noticed here because a full consideration of them would lead us too far into descriptive details, and we must be satisfied with remarking that they are intermediate in their whole structure between Tuberaceae and typical Discomycetes, especially the Pezizae; they are evidently closely related to both groups. We are indebted to Tulasne for the little that we know of the origin of the sporo- carps in Tuber, and from this they would appear, as has been already stated, to be formed inside a mycelial weft. The different regions and tissues are differentiated in them while they are still quite young ; the surface of specimens of Tuber mesentericum of the size of hemp-seed has the same structure and the same black colour as in those which are fully grown. Very little more is known than this. We shall have to wait for a complete knowledge of the history of development in these subterranean plants till we have succeeded in cultivating them. 3. Onygena corvina, A. S. grows on the feathers of birds of prey and the mycelium which spreads in them produces stalked spherical sporocarps. The stalk is 7-10 mm. in length and about 1 mm. in thickness, and consists of longitudinally parallel CHAPTER V.—COMPARATIVE RE VIEW.—ASCOMYCETES, 197 hyphae closely united together. It bears at its apex the spherical spore-receptacle which is about 2 mm. in diameter and has its dense hyphal weft differentiated into a wall or peridium composed of many layers of an unevenly floccose loose pseudo- parenchyma, and a spore-forming gleba within the peridium. The general form of the gleba is that of a flattened sphere; it consists of closely interwoven and very copiously branched hyphae, which produce everywhere countless asci in dense tufts on the extremities of their branches. The asci are comparatively small ovoid bodies containing each eight delicate ellipsoid spores, which are released when ripe by the disappearance of the membrane of the ascus. When the entire mass of spores is ripe, the whole structure dries up, the peridium opens by a circular fissure and becomes detached like a cap, and the cinnamon-coloured spores are scattered like dust from the flocculent remains of the ascogenous hyphae. Onygena equina, P. a more robust form has, according to Tulasne, a precisely similar structure. 4. Myriangium Durieui grows on the rind of trees and forms a large, flat, black thallus from one to a few millimetres in size composed of a tolerably uniform narrow- celled pseudo-parenchyma with brown cell-walls. The sporocarps are protuberances on the outside of the thallus, and consist, as we know from Millardet’s researches, of a pseudo-parenchyma similar to that of the thallus, but of finer texture, between the cells of which spherical asci are everywhere distributed usually at some distance from one another. The sporocarp thus constituted occupies the middle of a round protuberance of the thallus in the earliest stages that have been examined. It then grows by constant formation of new cells in a meristematic tissue which lies on its inner side, the side which is turned to the substratum. From this tissue new layers of ascogenous parenchyma are thrust one after another towards the outside. In conse- quence of the pressure thus produced the original tissue of the thallus in this part is rup- tured, and the exposed ascogenous tissue breaks away as new tissue is pushed forward. The great capacity for swelling in the membranes of the ripe asci in the older tissue-layers favours theirremoval. The youngest ascilie near the layer of meristem between the cells of the pseudo-parenchyma, from which they are chiefly distinguished by their greater abundance of protoplasm. As they move towards the outside they grow to 8-Io times their original diameter and produce eight pluricellular compound spores ; the germina- tion of the spores is as little known as the further details of their development. ORIGIN OF THE SPOROCARP. Section LXIII. The first steps in the formation of the sporocarp (fruc- tification) of the Ascomycetes have up to the present time been closely studied in comparatively few species; the search for and clear preparation of the first com- mencements is in most cases difficult from the small size of the objects, and there is difficulty also in unravelling the hyphal weft. The subject has been investigated in a certain number of species in all the chief divisions of the group, and important differences, recurring in all cases in their most essential points, are found to exist even between species which resemble each other very closely in the more. advanced state. Intermediate forms are found between the several cases which differ extremely from one another. The whole series may be arranged in the following order. 1. Eremascus albus is the name given by Eidam to a small Mould which may be cultivated in nutrient solutions, and which has a filiform septate many-celled mycelium. To form the sporocarp (Fig. 92) two adjoining cells of the mycelium put out each a lateral branch (a) close by the transverse wall which divides them. The two branches are from the first in contact with one another; they are exactly alike, and they grow coiling spirally round one another to a length exceeding the 198 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI. transverse diameter of the mycelial hypha 10 times or more (4). Then they cease to lengthen, are delimited from their parent-hyphae and conjugate at their summits, the cell-walls disappearing at the point of contact and the two protoplasmic bodies coalescing into one (c). The place of conjugation then swells into a spherical vesicle, which is delimited when the protoplasm of the pair of cells has passed into it, and having thus become an ascus forms 8 spores capable of germination (d-/). The spores are formed, as far as can be gathered from Eidam’s somewhat superficial description, in the manner described in section XIX. No further complications have been observed in the formation of these sporocarps. 2. Distinct archicarps are formed as branches on the mycelium or on vegetating hyphae in the thallus singly, or rarely in groups, as in Pyronema and Physma. It ‘depends on the species whether the archicarp is a single cell or, as is more com- monly the case, a cell-row, and whether it is spirally coiled or of some other shape. ‘The whole ascus-apparatus of the sporocarp is derived exclusively from the archi- carp. In Podosphaera a single ascus borne on a short stalk-cell is formed by transverse division of the uni- cellular archicarp; in other species ascogenous hyphae sprout as branches from the archicarp, or the cells of the archicarp divide into ascogenous daughter-cells, that is, into daughter-cells which sprout out into asci. The archi- carp takes no part in the forma- tion of the envelope-apparatus, that is, of the wall, receptaculum, excipulum, paraphyses, &c. This gee Somes meek cc eee oe wre ty bas -ite ong ee ree matured and the spores formed in it. After Eidam. Magn. goo times. branches which arise in the neigh- bourhood of the archicarp, usually at its base, and grow round the ascus-apparatus in a way which is determined by the species. From this specific ascogenous function the archicarp may in this case be termed an ascogonium. It has also been called a carpogonium. Of cleistocarpous and pyrenocarpous forms the Erysipheae, Eurotium, Penicillium, Sordaria (Hypocopra), and Melanospora parasitica belong to this section; of gymno- carpous and discocarpous forms Gymonoascus, Pyronema, Ascobolus, and the Collemaceae which were examined by Stahl (Collema, Synechoblastus, Leptogium, Physma, &c.), In a number of.the species of this division an antheridial branch makes its appearance in characteristic form in connection with the archicarp béfore the com- mencement of the formation of asci. This is the case especially with Pyronema, the Erysipheae, Hypocopra, Gymnoascus, and Eurotium. In Pyronema, before further development begins, conjugation, the union of the two protoplasmic bodies. into one, takes place between antheridial branch and archicarp, by means of a special appa- ratus belonging to the archicarp, the “¢richogyne, and the same thing happens in less striking form in Eurotium, In the Collemaceae the antheridial branches are é CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES,. 199 formed separately from the archicarps in special layers or receptacles, the spermogonia, and give off small spore-like cells, the spermatia, by abscision. The spermatia are conveyed to the archicarp and to a special receptive process of it, the trichogyne, and conjugate with it. ‘These phenomena correspond in part, and, excepting in some points of detail which will be described further on, to those observed elsewhere in distinct sexual organs and processes, and without them the sporocarp is not developed. The organs here described in the Ascomycetes are therefore to be regarded in the above cases as sexual organs, the archicarps as the female, the antheridial branches or spermatia as the male organs. In the Erysipheae, Penicillium, Sordaria, and Gymnoascus conjugation has not been observed, but the union of the two kinds of organs is as firm as it is invariable. Their sexual function therefore has not been certainly proved, but it may be assumed to be highly probable. The antheridial branches are less constant and less distinct in Ascobolus and Melanospora. According to present observations they are not to be clearly dis- tinguished from the first envelope-filaments that grow round the archicarp; their sexual function must therefore be considered to be undetermined. The question of the homologies is not hereby prejudged, as will be explained in section LXVI. 3. An archicarp is formed in the compact thallus of Polystigma rubrum and P. fulvum very similar to that of Collema, and in this case also the archicarp alone produces the ascogenous hyphae at a later period. Spermogonia and spermatia are likewise present, but the union of the latter with the archicarp has not been cer- tainly observed, perhaps owing to their extreme delicacy. Moreover the archicarp here makes its appearance inside a delicate (pseudo-parenchymatous) hyphal coil pro- duced at first as a new formation in the thallus, which may be termed the primordium of the sporocarp, and from it the envelope-apparatus of the sporocarp is subsequently developed under conditions of new formation and resorption. The archicarp is a long, coiled row of many cells. In this respect it is like the archicarp of the Collemaceae, and one extremity of it projects as in that group in the form of a trichogyne above the surface of the thallus, while the lower coils are concealed in the primordium, Before the formation of asci commences, these coils are found to be divided into portions containing from one to several cells and distributed in the future hypothecium, and from here they put‘ out the ascogenous hyphae in the form of branches; but the portion which protrudés’ as the trichogyne perishes without taking any direct part in the formation of asci. All these phenomena are exactly similar to those observed in the Collemaceae, as will appear from the special description of a subsequent page, with the exception of the union of the spermatia and the presence of the primordium from the first concealing the archicarp, neither of which has yet been ascertained. 4. The processes observed in Xylaria again are similar to those in Poly- stigma. First the appearance of a delicate primordial hyphal coil in the thallus; then inside that of a coiled row of large cells similar to the archicarp of Polystigma (named by Fiiisting Woronzin’s hypha); finally of cell-groups distributed in the —hypothecium: from which the asci sprout, while Woronin’s hypha is to a great extent at léast disorganised and disappears. But a piece of Woronin’s hypha projecting from the primordium, a trichogyne, has not been observed, and there- fore no visits of spermatia to it; nor is there any proof of genetic connection 200 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI, between the ascogenous cells distributed in the hypothecium and Woronin’s hypha. Considering the difficulty of getting at the young states of these sporocarps the data before us leave it open to possibility that both Polystigma and Xylaria do really behave like Collema, only certain initial and intermediate states being at present unknown, and that we shall at length discover organs in Xylaria equi-. valent to spermatia. But if what we at present know is the full account of the matter, then Xylaria is distinguished from Polystigma, and of course still more from all the forms mentioned in number 2, by the fact that the ascogenous cells and hyphae do not spring from a distinct archicarp, but, like the paraphyses, from parts of the primordium, while the archicarp, unmistakeably present in form as Woronin’s hypha, perishes without taking part morphologically in the formation of asci, 5: The difference from the first case is still more distinct in certain dis- cocarpous Lichen-fungi which have been examined by Krabbe (Sphyridium, ‘ Baeomyces, Cladonia), in Sclerotinia and in a number of Pyrenomycetes. Ascogenous and envelope-hyphae are everywhere inserted between one another and are closely interwoven in the hypothecium of the long-stalked cup of Sclerotinia Sclerotiorum, but a direct genetic connection, an origin of the two from a common source, can nowhere be shown; the lowest extremities of both pass into the uniform sterile tissue which ascends from the stalk. It is nevertheless highly probable that the two kinds of elements have a separate origin from the commencement of the formation of the cup, for small round coils of very delicate hyphae are formed in the sclerotium beneath the rind before the cup emerges from it. ‘The commence- ment of a cup always rises from above a coil of this kind as a comparatively thick bundle of hyphae, the innermost of which are branches of the hyphae of the coil, while the much more numerous peripheral hyphae originate in the surrounding tissue of the sclerotium. It is probable that the latter represent the envelope-apparatus, and those from the coil the ascogenous portion of the cup, and that the coil therefore is a kind of ascogonium. But a distinct proof of this has never been forthcoming, because, as the stalk elongates, it is no longer possible to show a morphological distinction between the two elements and by this means to establish the connection between the later ascogenous hyphae and their supposed primordia. Neither anthe; ridial branches nor spermatia were observed during these developments. In the Lichen-fungi mentioned above, the ascogenous hyphae may be seen, according to Krabbe, distinctly marked between the hyphae of the envelope- apparatus at a very early stage in the development of the sporocarp. But no initial organ has been observed from which they originated, and it must be presumed that they both have a common origin in the hyphae of the vegetative thallus or of the primordium of the sporocarp, and without the co-operation of spermatia or antheridia. ; In the Pyrenomycetes, Claviceps, Epichloe, Pleospora, and perhaps also Nectria, no co-operation of the above-named organs has been observed, and no distinct ascogonium, The young perithecium, as at present known, is a body consisting of similar hyphae or parenchymatous cells, and its elements are gradually fashioned and differentiated into the parts of the perithecium; in this process a cell- group occupying the position of the hypothecium undertakes the formation of the asci, CHAP. V.—COMPARATIVE REVIEW.— ASCOMYCETES.—ERYSIPHEAE. 201 and in Pleospora and Nectria the paraphyses are even formed from the same group, Hartig’s conjecture with regard to Nectria may certainly hold good of Claviceps and also of Epichloe, that special ascogenous initial organs are really present on the very young stroma, but up to the present time have been overlooked; as regards Pleospora we have only Bauke’s somewhat imperfect preliminary communication. With the accounts at present before us our knowledge is limited to the alleged mode of differentiation. If we choose to speak of ascogonium or archicarp in these genera, we must apply the term only to the initial organs which are late in forming and not very distinct in their differentiation. Van Tieghem’s discomycetous genus Ascodesmis would belong to this series, if that writer’s not very complete account of it is correct. We now proceed to give the details which are necessary for the full under- standing of what has been said above, and to add some supplementary observations, The arrangement of the material is for perspicuity’s sake somewhat different from that adopted in the foregoing account. FIG, 93. Podosphaera Castagnet on Taraxacum. Development of the sporocarp. Stages of the development according to the letters F—N.. o superior, « inferior mycelial filament, a antheridial branch, archicarp. In G the envelope is beginning to form, in H the outer wall is complete. Ka young sporocarp quite transparent. JV a similar one in optical longitudinal section ; s an ascus, x the outer wall, 7 the cells of the inner wall formed from the outer, Magn, 390 times. ‘ Sxction LXIV, 1. Erysipheae (Fig. 93; see also Fig. 107), The mycelium of these epiphytic parasites is composed of branched septate hyphae which spread over the surface of the host, being attached to its epidermis by the haustoria described in section V, and frequently touch and cross one another. The formation of a sporocarp begins at the point of contact or crossing of two branches. The process is of the simplest kind in Podosphaera. Two branches put out short protuberances at the same time, which rise erect from the surface of the epidermis and are soon delimited by a transverse wall. The one which proceeds from the lower of the two branches where they cross takes the form of an elongated ellipsoid cell, 2—3 times the length of the transverse diameter of the parent-branch, and is the archicarp. The other, the antheridial branch, remains cylindrical in shape, being of the same breadth as the mycelial hypha from which it springs or a little narrower ; it is always closely applied to the archicarp, and its upper extremity 202 DIVISION I1,—COURSE OF DEVELOPMENT OF FUNGI, bends over and covers the apex of the archicarp, and it is presently delimited by a transverse wall, forming a short nearly isodiametric cell, the ‘antheridium,’ which is borne on the lower part of the branch as on its stalk. The archicarp now developes into the sporocarp, being usually divided by a transverse wall into two cells, an upper which becomes the solitary ascus and subsequently produces eight spores, and a lower which as a stalk-cell bears the ascus. Tulasne has found two asci in a sporocarp as a very rare and individual exception; they were probably caused by the formation of two transverse divisions in the archicarp-cell. The envelope-apparatus also begins to be formed at the same time as the ascus. From 7-9 tubular outgrowths appear close round the base of the archicarp on the hyphae which bear it and the antheridial branch, and grow up round it and in close contact with it and in close lateral: contact with one another and with the antheridial branch, till they all meet together above its apex. Each tube then divides by one or two transverse walls, so that the incipient sporocarp is surrounded by an envelope formed of a single layer of many cells. These cells then increase in size. in the surface-direction, their walls thicken by degrees and assume a dark brown*colour, and they thus form the outer wall of the sporocarp. During this time they form no further divisions, but those nearest the substratum send out rhizoid branches which spread over the substratum ; and in some, but not all, species some of the cells at the apex of the sporocarp form a number of hairs with delicate ramifications which are described urider the name of afpendiculaé. Branches shoot out at an early period from the inner surface of the cells of the outer wall, which insinuate themselves between it and the growing archicarp, and ramify and develope into a dense parenchyma-like weft without interstices formed of two or three or more layers of cells according to the species; this weft has been termed the zamer wall of the sporocarp and compared from its origin and arrangement with the paraphyses of more highly differentiated sporocarps. With these formations the sporocarp in its envelope is complete in all its parts, and they are followed by further considerable increase in size only, which in the end chiefly affects the ascus and leads to a partial displacement of the cells of the inner wall. The antheridial brarich separates from the archicarp when the branches begin to be formed from the inner wall; it takes part with less increase in size of its parts and less considerable change of shape in the formation of the outer wall, between the other cells of which it remains laterally enclosed. The development of the sporocarp of the species of Erysiphe, under which genus I include all the Erysipheae which do not belong to Podosphaera, agrees with the above description except in certain points, the chief of which only will be pointed out in this place; the reader is referred for further details to the account given in another work’. The archicarp has the form of an elongated club- shaped cell, curved spirally round a hooked antheridial branch. The two organs are surrounded and enclosed by the tubes of the envelope, which give rise, as in Podosphaera, to the outer wall of the sporocarp and to the inner wall which is much more largely developed in these species. The antheridial branch enclosed in the inner wall soon disappears from observation, The archicarp on the other hand, lying in the basal portion of the sporocarp, grows into a curved tube -and Beitr. z. Morph. u. Phys. d. Pilze, IIL. CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES.—EUROTIUM. °203 divides by transverse walls into a row of several cells, from which a number of -broadly club-shaped erect asci are formed by each cell of the row growing out directly into an ascus, or putting out a few short branches which terminate in asci and are therefore ascogenous. In both Erysiphe and Podosphaera the formation of the envelope is at first in advance of that of the asci, and is nearly finished when the asci or the cells which produce them are still quite small, and it is not till the last stage of the development that the growth of the asci advances, chiefly at the expense of the tissue immediately FIG. 94. Eurotium repens. A branch of the mycelium with a gonidiophore ¢ and young archicarps as; s¢ sterig- mata. J spirally twisted archicarp ¢s with the antheridial-branch 7 and an envelope-branch. C older specimen with a larger number of envelope-branches growing round the archicarp; / antheridial branch. D young sporocarps seen from without. Zand F other young sporocarps in optical longitudinal section. In £ the inner wall is beginning to be formed ; w the outer wall, 7 the inner wall-cells and the cells filling the space between the ascogonium and the wall. as the ascogonium. Gascus with spores. H ripe ascospore of £. Aspergillus glaucus isolated. A magn. 190 times, the rest of the figures 600 times, \ surrounding it. The spores are in most cases formed as soon as the asci have reached their full size; but in some species, as Erysiphe Galeopsidis and E. graminis, (Wolff), there is a pause in the development before the formation of the spores, and further progress only takes place under favourable conditions of temperature and moisture after a resting period of some duration which happens to fall in the winter- time ; the protoplasm of the tissue of the inner wall is evidently employed to form the spores. 2. The archicarp of Eurotium (Fig. 94) is produced by the gradual basi- petal coiling of the extremity of the upper end of a branch of the mycelium into 204 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI, the shape of a hollow spiral with four or five turns which lie close to one another. The spiral is divided by transverse walls into about as many cells as there are turns. Then two or three slender branchlets grow from the lowest turn in the direction of the apex, and are closely applied to the surface of the spiral; one of these gets in advance of the rest and is the first to reach the apex; there it lays its upper extremity on that of the spiral filament, and, if we may trust our observations, the two filaments conjugate, that is, their protoplasmic bodies unite by the dis- appearance of the intervening membranes. Sometimes the branch which anticipates the rest is seen to grow up inside the spiral, and then the conjugation cannot be so certainly ascertained; from its behaviour it must be regarded as the antheridial branch. When it has reached the apex of the spiral it is followed by the rest, and now all of them put out new branches which become so interlaced and divided by transverse walls that the spiral is soon covered by a compact layer of isodiametric cells. The lowest turn of the spiral itself participates in the formation of this layer, which surrounds the rest of the spiral, the ascogonium-hypha, as the perfectly closed outer wall of the globular sporocarp. The cells of the outer wall do not divide again; but while the sporocarp increases considerably in volume they grow in the direction of the surface into a tabular form, and secrete on their outer membrane, which continues thin and colourless, a golden-yellow substance readily soluble in alcohol in the form of a thick brittle pellicle. Branches shoot out, as in Erysiphe, from the inner surface of the cells of the outer wall, as soon as these have united, and ramify and become interlaced and soon form an inner wall of many layers, while fresh branches from them push in between the loosening turns of the spiral, and fill the space between it and the outer wall with a tissue composed of thin-walled cells rich in protoplasm and without interstices. The growth of this tissue causes the sporocarp at first to increase in volume in every direction and constantly forces the coils of the spiral ascogonium further apart. When it has reached a certain point, the spiral begins to put out numerous branches, the ascogenous hyphae, which thrust themselves in between the inner wall-cells in every direction, and replace them, and the many extremities of their numerous ramifications become ovoid eight-spored asci. The continuity of the ascogenous hyphae is more and more lost as the asci are formed, so that as the spores begin to ripen the outer wall encloses only asci and the remains of the hyphae and the cells of the inner wall, and at length the walls of the asci themselves disappear and the sporocarp contains scarcely anything but ripe spores. 3. According to Brefeld’s researches, the development of the sporocarps of Penicillium glaucum also begins with the appearance of a spirally twisted hyphal branch. But here we-find in the first stages that are open to observation two similar branchlets surrounded by felted mycelium, which always arise close to one another and are spirally twisted round one another in one or two turns; whether they are morphologically and physiologically of equal or unequal value cannot be directly determined, and the further development gives no certain information on this point, so that we can only speak of a distinction between archicarp and antheridial branch of like form with it from the analogy of the otherwise nearly related Eurotium, Then from the spirally twisted body—whether from one only of its component parts or from both is not ascertained—short ascogenous hyphae grow out as branches CHAPTER V.—-COMPARATIVE REVIEW.—ASCOMYCETES.—PENICILLIUM, 205 in every direction, and at the same time numerous branches begin to be formed on the neighbouring mycelial hyphae which grow rapidly round the others, and inclose them in a compact envelope composed of from 8-16 layers of cells which leave no interstices. The elements of this enveloping weft thrust themselves everywhere in between the ascogenous hyphal branches; in their early states they are much narrower than these and therefore easily distinguished from them in section. The spherical sporocarp which. in this state is about 0.05-0.09 mm. in size now increases to an average size of o.5 mm. and more, and this increase is chiefly due to the enlargement of the cells of the envelope. The great mass of the inner substance is the part most strongly affected, and its cells become irregularly polyhedral and colourless, and are provided with much thickened pitted cellulose-membrane and. hyaline cell-contents which turn dark yellow.with iodine. The membranes of the cells of two or three peripheral layers become yellowish brown in colour and form a thick’ " persistent outer wall, while a few layers on the outside do not share in the thickening: and are cast off when the sporocarp is ripe. With the commencement of these changes the ascogenous hyphae elongate and force themselves in between the growing tissue of the envelopé in irregular courses in every direction. In doing this they do- not appear to form many new branches or to increase-much in breadth, and the latter is the case also with the cell-layers of the envelope which are in contact with them. In sections through an older sporocarp we therefore find in the interior in the large- | celled tissue of the envelope ascogenous hyphae cut through in various directions, transverse, oblique or longitudinal, accompanied by small-celled tissue. The cell-walls’ of these ascogenous hyphae also become thickened, and when this thickening has reached a certain point in them and in the envelope, there is a pause in the develop- ment, a resting condition. This lasts 7-8 weeks, if the sporocarp is placed as soon as it is ripe in moist surroundings which are favourable to further development ;° but the resting state cannot last much longer, according to Brefeld’s observations, if the surroundings are dry, for dry sporocarps 3-4 months old proved incapable of further development. If the sporocarps are placed within the time stated on a moist substratum in a suitable temperature, they recommence their development ; the ascogenous hyphae begin to branch copiously, the branches grow at the expense of the colourless tissue of the envelope which is by degrees entirely dissolved, and again branch, and at length a large number of small eight-spored asci connected together in rows and resembling those of Eurotium are formed on branches of the last order. There only remains at last of the whole sporocarp the pores and the brownish yellow outer wall, which forms a loose envelope round them. Of the details of these changes which may be obtained from Brefeld, it will be sufficient to mention here, that the branches formed on the ascogenous hyphae are of two kinds; comparatively slender ones which penetrate between the cells of the tissue of the envelope, ramify copiously in it and are evidently used to effect the dissolution of that tissue and to take up the products of the dissolution, but do not form asci; and secondly, thicker much curved forms with short branches of their own, from the ramifications of which the asci are ultimately produced.. These facts recall the two forms of hyphae in the ripening sporocarp of Elaphomyces (see page 193). The entering of the sporocarp on a resting period and the change from this to the formation of asci at the expense of the tissue of the envelope has its analogue in the 206 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. processes described in Erysiphe graminis and E, Galeopsidis, only that there the: resting-time begins after the formation of the asci, and the spores only have to be formed when vegetation reawakens, Van Tieghem? describes a Penicillium aureum, which is distinguished from P. glaucum, as regards the processes in question, by having no resting-period ; he asserts, that in this species both the initial branches which are spirally wound round one another are ascogenous, that is, that they both send out branches, the last ramifications of which are asci. The sporocarps of Aspergillus (Sterigmatocystis) niger and A. purpureus have, according to Van Tieghem ?, essentially the same development and structure as those of Penicillium; and Eidam’s new Sterigmatocystis nidulans, a remarkable plant in many respects, should also find its place here. 4. The sporocarps of Gymnoascus and Ctenomyces which live on animal excrements usually appear, according to Baranetzky, Eidam, and Van Tieghem, as small coils of felted tissue crowded together in heaps on the mycelium, the largest somewhat more than 1 mm. high, but most of them of much smaller size. Their formation commences with the union of two unicellular segments of the mycelial hyphae, one of which is wound round the other in a close spiral; the two cells arise close to one another as. lateral branches of one hypha, or spring from different hyphae, or only the one which is wound round the other is a lateral branch and the other is an intercalary member of a hypha. ‘The member that winds round the other is an archicarp or ascogonium. It ceases to grow in length when it has formed, a varying number of turns, and sends out branches instead, forming numerous rami- fications, which are woven together into a coil and have finally at their extremities. round eight-spored asci like those of Eurotium. The member, round which the ascogonium is coiled, and which, from the analogy of the cases previously described, must be called the antheridial branch, is cylindrically club-shaped and either coiled like the other cell or straight, and can no longer be distinguished by direct observation when it has undergone a moderate increase in size and become divided by a few transverse walls. It is not till the ascogonium begins to send out branches that the young sporocarp becomes loosely enveloped by a number of hyphal branches, which spring partly from the base of the ascogonium itself partly from adjacent branches of the mycelium, and have their membranes thickened and coloured yellow or brick-red ; the peculiar antler-like ramifications of these filaments loosely intertwined form . a lattice-like envelope composed of several layers round the ascogenous coil as it advances to maturity. Rhizoid branches also spread over the substratum. 5- The sporocarps of the species of Ascobolus (Fig. 95) when fully matured have the typical discomycetous form. They have the form of a broad short cone, the obtuse point of which is seated upon the filamentous mycelium while the broad basal surface is covered by the hymenium. ‘Their development would appear to be alike in all the species; the following account of it refers especially to Janczewski’s exact observation of the best-known species A. furfuraceus. The development begins with the appearance of an archicarp in the form of a comparatively thick arched lateral branch from a mycelial hypha; this branch becomes by successive divisions . 1 Van Tieghem in Bull. Soc. Bot. de France, XXIV (1871), p. 157. ? Loc. cit. pp. 96, 203. CHAPTER V.-—COMPARATIVE REVIEW.—-ASCOMYCETES.—ASCOBOLUS. 207 a series of simple apparently similar cells rich in protoplasm which grow to be about as long as broad, and then a preliminary cessation of this growth takes place. Slender branches which spring from the mycelium near the archicarp, and also branch themselves, now grow in the direction of the archicarp and apply themselves and their branches closely to its free extremity (Fig. 95 7). They behave in this respect like the antheridial branches of Eurotium and Erysiphe and may therefore receive the same name. Their contact with the archicarp is followed at once by the formation of a large number of fresh branches on the hyphae which produced them and on adjacent mycelial hyphae, and all these later branches grow closely interlaced round the archicarp and the first antheridial branches, which from this time cease to be distinguishable. The archicarp is thus at once inclosed in a compact hyphal coil, the envelope, which then grows considerably, partly by the introduction of new hyphal branches partly by the increase in size of those previously formed, the cells of which become vesicular and for the most part continue united together into a dense pseudo-parenchyma. A fewperipheral layers ~ of these cells form a thick-walled rind, which is yellow in Ascobolus furfuraceus from the colour of the membranes but is differently coloured in other species, and which sends rhizoid-hyphae into the sub- stratum at the points of contact, while in many species, but not in A. furfuraceus, it produces spreading hairs of peculiar form and arrangement. With all these changes the sporocarp assumes a spherical shape, and the course and direction of its growth are such that the archicarp remains in- closed in the dasal portion of the sphere where it rests on the substratum. The ection 2a young frucifcations o mycslinm, ¢ aebicare, formation of paraphyses begins at the same jayer and the sed dock, asthenidit branche pe teawe time as the differentiation of the rind im frammaticaly represented by Sechs after Janene the opposite apical region, and their first beginnings appear as branches from a zone of narrow cells still rich in protoplasm in the tissue of the envelope, “he subhymental zone, which passes across the apical region beneath the rind. The paraphyses are formed as slender hyphal out-growths in this region; each of them can send out new and similar branches of more than one order near its point of origin. But the ends of the branches of every order grow into slender long-celled filaments which constitute the paraphyses, and converging at first have all a direction from the subhymenial zone towards the apical region of the rind and end below it. In proportion as they elongate and increase in number by the introduction of new branches from the subhymenial region and whilst the surrounding parts follow these processes of growth, the space between the rind and the subhymenial layer grows broader, but is always being filled up by the paraphyses which are arranged close beside one another as the first commencement of the hymenium. It may be observed here by anticipation that the growth of the hymenium continues 4g 208 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. longer in the surface-direction, while the rind covering it does not grow correspond- ingly, and the rind is therefore ruptured above the hymenium, which is thus exposed as a discus. Up to the time of the inception of the hymenium beneath the rind no changes of importance take place in the ascogonium. But now all its cells except one are seen to become thick-walled and poor in protoplasm, and in this state they continue permanently; but that one cell, the third or fourth uppermost cell, becomes the ~ initial cell of the formation of asci, the ascogenous cell. It is full of protoplasm and swells considerably, and then sends out twelve or more strong cylindrical branches from its free outer surface. These are the ascus-forming branches, the ascogenous hyphae, and they thrust themselves in between the elements of the tissue of the envelope as they grow in the direction of the subhymenial layer, into which they send their many branches and spread abroad between the points of insertion of the paraphyses, Finally the asci appear as lateral branches of the last order on these subhymenial spreading hyphae, which, as has been already said, grow between the paraphyses and in the same direction with them towards the outer surface of the hymenium. The long-continued successive formation and introduction of new asci at all points is the chief cause at least of the surface-enlargement mentioned above, and of the exposure and often even of the convexity outwards of the hymenium. Janczewski’s observations have been confirmed in the case of several species by Borzi, who has also described an allied form, a species of Ryparobius, in which every shoot from the ascogenous cell becomes an ascus directly. Borzi’s view respecting the fertilisation of the archicarp is not supported by any other case. . 6. The development of the sporocarp of Pyronema confluens (Peziza, P.) was described by myself, but imperfectly, in 1863. Tulasne then added something to my statements. Kihlman’s recent examination of the species gives the following results (Figs. 96-99). The Fungus spreads the stout filaments of its mycelium over wide spaces of ground, especially where charcoal has been made or fires have burned.’ The inception of the young sporocarp is preceded by the formation of groups of obliquely erect curved branches, which in their turn put forth many branchlets. Some of these, usually two in each group, swell strongly and form a few short bifurcations, which grow in a direction vertical to the substratum and then cease their longi- tudinal growth. The bifurcations form together an erect loose tuft or rosette (Figs. 96, 97 A), and some of them terminate in a short roundish cylindrical cell which remains sterile. The extremities of others become either archicarps or antheridia (Fig. 97 A, 2). The former are broadly club-shaped bodies consisting of a much inflated and usually somewhat curved cell, densely filled with protoplasm and borne on one or two disk-shaped stalk-cells; the antheridia are the club-shaped terminal cells of the branches of the bifurcations, about the same height, but only half as broad as the archicarps. Several, at least two or three, organs of both kinds are present in each rosette, and no other relations than those stated between the points of origin of each pair of dissimilar organs have ever been observed. When the two kinds of organs have reached the shape and length which have been described, each archicarp puts out a broad protuberance near its apex, which grows rapidly into a blunt cylindrical tube filled full with protoplasm ; and the tube becoming bent like a bow in a plane differently disposed in different individuals, grows on towards.a neighbouring antheridium, and CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES.--PYRONEMA. 209 embraces its apex and presses its obtuse extremity firmly against it. When this has taken place, seldom before, the tube is delimited by a firm transverse wall from the inflated portion of the archicarp, and, as soon as the wall is formed, the membrane in each of the connected organs is dissolved at the point of contact of the tube with the antheridium, and the protoplasmic bodies of the two organs unite together through a broad aperture (Fig. 97 2). The bent tube is therefore an organ which affects an FIGS. 96—99. Pyronema confluens, Tul. FIG. 96. Rosette of antheridia and archicarps on the mycelial filaments #2; _/ first beginnings of the filaments of the envelope. Magn. 190 times. FiG. 97. 4 asmall rosette of incipient sporocarps; ¢ archicarps, @ antheridia, ¢ a trichogyne which has not yet entered into union with a2. B from an older rosette; the trichogyne ¢ proceeding from the archicarp c and cut off by a transverse wall is in open communication with the antheridium @. Ca pair of organs isolated, from a young sporocarp in about the same stage as Fig. 98; @ antheridium in communication through ¢ with an archicarp ¢, which is much swollen and has put out branched ascogenous hyphae from its surface. After Kihlman’s preparations and drawings. Magn. about 300 times. FIG.98. Young sporocarp in water showing through the cover-glass. The group of antheridia and archicarps is densely overgrown by hyphae of the envelope which have formed erect paraphyses above; the archicarps appear through the envelope-weft as large vesicles. Magn. go times. FIG.99. Median longitudinal section through a sporocarp in the process of maturing. Archicarps and antheridia can no longer be distinguished, and many asci have been formed between the paraphyses. (See Fig. 39.) Magn. about 45 times. union between the archicarp and the antheridium and, in accordance with the terminology which is in use in other cases and which will be further considered below, may be termed a “richogyne. ‘Conjugation is followed by increase in size in the archicarps, and by the formation of protuberances in a dozen or more places scattered over the surface of each archicarp, which develope into thick short-celled ascogenous hyphae (Fig. 97 C). Simultaneously with this, or even before it, copiously branched [4] P 210 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. hyphae begin to shoot out from the sterile sister-branches of the archicarp and from the whole of the rest of the basal region of the rosette to form the envelope-portion of the sporocarp (Fig. 98), consisting of a receptaculum enclosing the group of archicarps and antheridia and the hypothecium with the paraphyses, which latter always rests free on the receptaculum without an enveloping wall. The dis- tribution of the ascogenous hyphae and asci and the gradual multiplication of the latter between these elements of the envelope are essentially the same as in Ascobolus. The paraphyses form at first a conical tuft on the hypothecium, which generally broadens out into a disk through the introduction of newelements. The receptaculum becomes a comparatively large thick large-celled pseudo-parenchymatous disk covered with rhizoids, and between its elements those of the primary rosette are inclosed, and are at length indistinguishable (Fig. 99). The antheridia continue longest visible and indeed almost unaltered, being very full of protoplasm, and take no part in the formation of the envelope. 7. InSordaria among the Pyrenomycetes especially S. (Hypocopra) fimicola and in Melanospora parasitica the course of development in the perithecium, according to Gilkinet’s and Kihlman’s researches, is essentially the same as in Ascobolus, of course with certain specific differences, and with differences of conformation corre- sponding to the difference between Discomycetes and Pyrenomycetes. The archicarp is a spirally coiled cell-row, though in Melanospora it is sometimes almost-straight. _ Antheridial branches are less plainly seen in Melanospora, or at least are not sharply distinguished from the incipient filaments of the envelope, which here too grow close round the archicarp soon after its formation. In Sordaria the growing archicarp divides by transverse walls into numerous cells, and ascogenous hyphae sprout from the great majority of these cells; whether any portion of the archicarp takes no part in their production could not be determined owing to the early gelatinous disorganisation of the walls of all its cells. In Melanospora only one or two cells in the middle of the large archicarp become ascogenous, the rest being disorganised and afterwards partly ejected in this state from the orifice of the young perithecium. These one or two ascogenous cells develope by successive bipartitions in varying directions into a parenchymatous body, the many cells of which are full of protoplasm and subsequently produce the asci. These are arranged in Sordaria nearly parallel to one another in a thick tuft, in Melanospora they form a nearly spherical body, and their apices converge towards its middle. In both cases the many-layered pseudo- parenchymatous wall of the perithecium is formed from the weft of hyphae of the envelope. It is a spherical body at first closely surrounding the future group of asci on every side, the neck and the canal of the ostiole being formed in it later. ‘There are no paraphyses standing between the asci; these are placed separate and beside each other on a surface of insertion which covers a part of the interior of the sphere. On the side left free from the paraphyses there is a narrow empty space between the wall and the ascus-group, but this is soon filled with a large number of closely packed hyphal branches, which grow into it as perzphyses from the wall, converging radially till they touch one another. The group of these which is mostly turned away from the asci then grows vertically towards the wall in the direction of the neck which is to be, and so on to the outside through a hole in the wall, and thus forms the commencement of the neck, which may lengthen out considerably, and in Sordaria is CHAPTER V.— COMPARATIVE REVIEW,—ASCOMYCETES.—COLLEMACEAE, 211 covered on ihe inside with periphyses which converge towards the median line. All the periphyses, those of the neck as well as those beneath it, converge till their extremities touch, but without becoming firmly united, so that asci or spores can. pass between them to the outside when they are mature. In Melanospora parasitica the future canal of the ostiole is to some extent marked out from the first, for the non-ascogenous basal cells of the spiral archicarp, that is the cells turned towards the place of insertion, remain in their place as large vesicles, together forming a strand outside which the periphyses which converge towards it afterwards spring from the wall. Then the neck also grows in the direction of the strand outwards at the place of insertion of the perithecium or archicarp, while the vesicles are ejected as disorganised masses of mucilage, In Sordaria it would appear that the canal of the ostiole and the neck are formed on the side diametrically opposite to the place of insertion of the perithe- - cium; the first simply in consequence of corresponding surface extension of the young wall, and as an intercellular space which ig at once filled with the periphyses; the formation of the neck has been less exactly studied. According to Van Tieg- hem’s observations Chaeto- ‘mium is nearly related to the forms which we have been considering. The con- clusions of this writer have, it is true, been stoutly as- sailed by Zopf, but on the other hand they have been recently confirmed by Eidam, and rightly as far as I can FIG. 100. 4, B Gyrophora cylindrica. A a vertical median section through a spermogonium imbedded in the thallus; 0 upper, 2 under rind, # medullary layer of see. Some particulars are the thallus. 2 portion of a very thin section from the base of the spermogonium ; w its wall from which proceed sterigmata with rod-like spermatia s, # medullary hyphae still doubtful, and should be of the thallus. C Cladonia Novae Angliae, Delise; sterigmata with spermatia from the spermogonium. After Tulasne. 4 magn. 90, B 390 times, C highly magnified. submitted to further exam- * ination with due reference to the works of these observers. The latter remark will . apply also to Bainier’s short description of some species of Ascotricha examined by him and ferhaps belonging to this place; I have not been able clearly to understand his account of them. 8. The development of the apothecia in the Discomycetes which are included in the group of the Collemaceae is in all points similar, according to Stahl’s observations, to those which have just been described. But it is preceded by fertilisation of the archicarp by spermatia formed at a distance from it, and this causes the following modifications. The Collemaceae form a gelatinous Lichen-thallus with lobe-like branches (see section CXVI. 5). Sections through the thallus show much-branched hyphae loosely distributed and interwoven in the thick gelatinous membrane-substance ; the branches are also closely united together at certain spots in the fertile thallus in order to form the receptacles which produce the spermatia, and which were first clearly distinguished by Tulasne as spermogonia. These organs, of which Fig. 100 below will give some idea, though taken from other species, are in the mature state small bodies, but visible to the naked eye, having very much the shape of the flask-shaped perithecium of the P 2 212 DIVISION II,—-COURSE OF DEVELOPMENT OF FUNGI. Pyrenomycetes protuberant below and with a short neck ; they are sunk in the thallus but have the free extremity of the neck on a level with the outer surface. The neck is traversed throughout its length by a canal open at both ends, the canal of egress. The wall of the inner ventral portion, which is formed of a close weft of hyphae, bears a hymenium on its inner surface composed of delicate hyphal branches of uniform height closely packed together, and converging in the direction of a central space which is free from them and is in open communication with the neck-canal. These hyphal branches behave like basidia or sterigmata, and abjoint serially and successively numerous spermatia at their apices in the form of small cylindrical rod-like cells. The apparently homogeneous protoplasm of the spermatia has a sharply defined contour, outside of which is a hyaline jelly, which swells and deliquesces in water and forms probably the outer layers of their membrane. In this gelatinous envelope the spermatia when abscised lie at first in the central cavity of the spermogonium and remain there as long as it is kept dry. If the water finds its way in, the jelly swells y, & x lie VV rh PX 1% os WS c ve g CX B XxX FIG. 101. Collemamicrophyllum, A transverse section through the thallus; # the hyphae, ¢ the Algae (see section CXVI), a the trichogyne projecting above the surface’of the thallus ; the spirally twisted archicarp which is imbedded in the thallus terminates in the trichogyne. B a younger archicarp drawn separately. C, D summits of trichogynes with spermatia attached projecting above the surface of the thallus which is shown by the horizontal lines. After Stahl. .4 magn. 350, the rest 7so times. and forces them out of the neck on to the surface of the thallus, over which they are distributed if there is sufficient moisture, as can be seen by transferring them to a drop of water on a microscopic slide, where they move in a slow uncertain manner, due no doubt to the currents in the dissolving jelly. The formation and discharge of the spermatia usually precede the appearance of the commencement of the apothecium, as will be noticed again below. These, the archicarps or carpogonia, are formed in most species of the group, in Collema, for example, beneath the surface of the thallus, and singly as lateral branches from hyphae which have nothing else to distinguish them. They are rather broader than the parent-hyphae and coil up near their point of origin, forming usually two or three narrow turns of a spiral, and then lengthen at the free extremity into a straight or slightly curved filament, which grows towards the surface of the thallus and out beyond it into the open air; here it often forms a narrow flask-shaped expansion and ceases to grow in length when the portion outside the thallus is about from four to six times as long as broad (Fig. 101). CHAPTER V.—COMPARATIVE REVIEW,—ASCOMYCETES.—COLLEMACEAE. 213 The further development shows that the spirally coiled portion of the archicarp is the ascogonium or place from which the formation of the asci proceeds, while the elongated part with its point projecting above the surface of the thallus is the “zcho- gyne, serving as the receptive-organ in fertilisation and conveying its influence to the ascogonium. Both parts are divided as they grow by transverse walls into cylindrical cells, of which there are about twelve in the ascogonium and as many or more in the trichogyne; they are all at first thin-walled and filled with a homogeneously hyaline protoplasm. The formation of archicarps generally takes place under the same external conditions as the discharge of the spermatia; namely, in the cool, damp, rainy period of the year. If the spermatia which have reached the surface of the thallus encounter the top of a new-formed trichogyne they attach themselves firmly to it often in great numbers, and notwithstanding the difficulty of minutely observing such small bodies when adhering to the comparatively thick trichogyne, Stahl was repeatedly able to assure himself that some of them put out a short process by means of which their protoplasm becomes united with that of the apex of the trichogyne (Fig. ror D). The effect of this union with the spermatia is seen in peculiar changes in the trichogyne, advancing from the apex to the base, and in the asco- gonium and surrounding parts, and these changes are not observed if no union takes place between trichogyne and spermatia. The changes are these; the cells of the trichogyne lose their turgidity and shrink into slender threads; their transverse walls only maintain their former breadth and at the same time swell strongly in the direction of the axis of the trichogyne, and thus form knot-like protuberances in the collapsed cell-row. The cells of the ascogonium continue turgescent, thin-walled, and rich in protoplasm, and increase in size and number by transverse divisions, Finally a large number of branches begin to be formed in the neighbourhood of the ascogo- nium on the adjacent hyphae of the thallus, and these ramifying repeatedly and inter- twining grow round the outside of the ascogonium and also push in between the turns of its spiral and force them apart; the ascogonium is thus rapidly inclosed in a mass of closely coiled filaments, the first-state of the envelope of the fructification. The coil is at first round and occupies the place in the interior of the thallus in which the ascogonium inclosed by it was first formed. When it has reached a certain size (Fig. 102), the hyphae on the side towards the adjoining surface of the thallus send out branches which again branch repeatedly, and the final ramifications are the first paraphyses which grow straight towards the surface of the thallus, pushing aside the tissue of the thallus which stands in their way, and terminate in it. At the same time the envelope-coil which was originally round increases in breadth in the direction of the surface of the thallus—chiefly no doubt by centrifugal formation of new hyphal branches on its lateral margin, so that it assumes the form of a concave disk cutting the surface of the thallus with its edges; and thus it developes into the ultimately pseudoparenchymatous excipulum, which continues for some time to increase in breadth at the margin which rests on the surface of the thallus. As the development of the excipulum advances, new paraphyses similar to the first shoot out one after another from its side towards the surface of the thallus, pushing aside the tissue of 1 The term was introduced by Bornet and Thuret to denote the analogous organs in the Florideae. See Ann. d. sc. nat. sér. 5, VII, p. 137. “214 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI, the thallus which is in their way, till at length the space between the excipulum and the surface of the thallus is filled by an incipient hymenium consisting of paraphyses standing side by side with no gaps between them. The ascogonium has meanwhile at first slowly followed the growth of the excipulum by intercalary growth accompanied by a loosening of the turns of the spiral. As the development proceeds the asco- genous hyphae sprout from it, and spread their abundant ramifications through the zone of origin of the paraphyses, the subhymenial layer, in essentially the same manner as in Ascobolus, and thrust the asci as branches of the last order one after another in between the paraphyses (Fig. 102). The species of Physma also examined by Stahl agree with Collema except in the following peculiarities. The archicarps here spring from the hyphae which form the protuberant base of the spermogonia, from four to eight on each spermo- gonium. The ascogonia are but slightly curved and are inclosed in the hyphal b. 0 Ai re an il eZ es iy us it i i iin i = Se i! 3 6 iy i ’. i My AM i ya i tk i eee | i ie VA Ds law a TA a (ul ZAR il: A) ie h Wg es BS NE ass io we Grae \ FIG. 102, Collema microphylium. Median section through a young apothecium imbedded in the thallus; % and gas in Fig. 101, 8—c excipulum and hypothecium ; from the latter proceed crowded upright paraphyses, between which asci are beginning to be formed on the ascogenous hyphae above the hypothecium. After Stahl. Magn. 530 times. weft of the wall of the spermogonium, and the trichogynes protrude beyond the outer side. The discharge of the spermatia of a spermogonium coincides as a rule with the completion of the trichogynes’which belong to them, and these become covered with the spermatia adhering to them. Then paraphyses grow out from the wall of the spermogonium into its now empty cavity, displacing the sterigmata, and soon fill it up in the form of a tuft of filaments which converge towards the former orifice and are so closely packed as to leave no spaces between them. Into the subhymenial zone, which is thus defined, ascogenous branches shoot out from the archicarps and push the asci in between the paraphyses; the spermogonium is thus converted into the apothecium. : Borzi has repeated Stahl’s observations on other species of the Collemaceae with confirmatory results. g. Incipient sporocarps or archicarps, of doubtful character and requiring a fresh examination, have been assigned by Woronin to Sphaeria Lemaneae, Sordaria CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES,—POLYSTIGMA. 215 fimiseda, Peziza granulata, and P. scutellata, and by Tulasne to P. melanoloma ; by R. Hartig to Rosellinia quercina and Nectria. 10. Polystigma rubrum and P. fulvum. The thallus of these Fungi forms compact disk-shaped stromata in the living tissue of the leaves of species of Prunus. It forms spermogonia, which resemble those of Collema in structure and produce curved filiform spermatia, At the same time or soon after, the primordia of the perithecia make their appearance in its interior. These are small coils of closely interwoven hyphal filaments, which are perfectly similar in structure in their early stages and show no manner of differentiation. The individual cells of the coil are distinguished from those of the thallus by their small dimensions and especially by turning yellowish brown, not blue (see page 9), with solution of iodine. As the growth of the coil proceeds the cells in its interior assume a more delicate appearance from diminution in thickness of their walls and become densely filled with protoplasm. A spirally coiled filament composed of broad and rather short cells, which comes out very beautifully when coloured with iodine, now becomes conspicuous among them. Its two or three turns extend through the entire space of the primordium, which in this stage is usually of an elongate ovoid form. The extremity of the filament rises above the primordium and passing through the cells of the mycelium penetrates to the surface of the leaf, where it finds its way through a stoma into the outer air, and has a perfect likeness to the apex of the trichogyne in the ascogonium of the Collemaceae as described by Stahl. The point is generally accompanied by more slender mycelial hyphae which grow out through the stoma when the trichogyne has decayed, and form a penicillate tuft of companion hyphae. Spermatia have been frequently seen to adhere to the summit of the trichogyne, but in no case has a more intimate connection, especially conjugation, been proved to take place. After some time the cells of the trichogyne-filament begin to die away from above downwards and to be no longer distinguishable in the tissue of the thallus, while the young perithecium enlarges at the same time throughout, the cells of its outer layers becoming elongated to form the wall. The remaining portion of the spiral filament, the ascogonium, also enlarges | its cells considerably and now appears as a thick highly refringent strand of cells. In Polystigma rubrum the young perithecium remains in this state during the winter, but the development goes on without interruption in P. fulvum, and consists in the up- ward growth of the envelope in a conical form and the flattening of the basal portion of the young perithecium, while the inner tissue swells at the same time into a jelly. The ascogonium lies irregularly distorted on the base of the young perithecium. The hyphal weft of the base of the perithecium sends in paraphyses between the cells of the ascogonium in the form of thick cell-rows with walls which readily swell into a jelly, while the upper part of the wall of the perithecium is covered with periphyses. The cells also of the ascogonium, all of them apparently, form protuberances which elongate into slender filaments with abundance of protoplasm and then branch, and soon become a mass of interlacing threads amongst the basal tissue of the paraphyses; these are the ascogenous hyphae, and their last ramifications grow upwards as asci, and as they increase in size they displace the paraphyses, which are then dissolved. The periphyses also disappear, and the basal tissue of the asci and paraphyses swells up and can 216 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. no longer be recognised, so that the perithecium in the mature state is broadly ovoido-conical with an indistinct ostiole. ‘The wall is formed of three or four layers of not much thickened elongated cells. Phyllachora Ulmi appears to show similarity to the process here described. 11. The club-shaped stroma of Xylaria polymorpha (Fig. 103) consists in the young state, according to my earlier observations, of a white medulla surrounded by a firm black rind. The former is composed of an air-containing tissue of colourless hyphae; the rind of the portion bearing perithecia consists of small-celled pseudo-parenchymatous tissue, which is overlaid on the outside by the hymenium which bears gonidia (see section LXXI) and ultimately disappears. The primordia \ SS) AvesBe OZ), 2 CAN ae SUN h9Me) || / Ne yt i) FIG. 103. Yylaria polymorpha. A, B, C transverse sections through young stromata with perithecia divided more or less exactly in half, all three magn. 90 times. » rind, #2 medullary layer of the stroma. 4, # very young perithecium cut through the middle, / a similar one cut through near the median plane, g older perithecia, # gonidial layer. 2B perithecium with the mouth # bursting through the rind. C a nearly fully developed perithecium; the section passes close to the mouth, which is fashioned as at g in 4, elsewhere through the median plane; / the outer, 7 the inner wall of the perithecium, x the large-celled paraphyses filling the centre of the perithecium having entirely displaced the short-lived inner tissue, A the inner surfaceof the wall with the insertions of the paraphyses and asci. of the perithecia (A, #) make their appearance in the form of small spherical bodies which lie in the medulla close beneath the black rind, and are at once distinguished from the medullary tissue by containing no air and therefore being transparent. They are formed of a closely woven mass of slender hyphae, which are much thinner than the hyphae of the original tissue and must therefore be a new formation in it. In somewhat older specimens an irregular large-celled coil of tissue is found lying in the middle of the sphere. The spheres now increase in size in the direction of the medulla, the shape, structure, and position remaining the same. Then a dense tuft of straight hyphae, in the shape of a broad truncated cone, shoots forth from the part which abuts on the rind, and elongates in the direction of the rind, which is CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES.—XYLARIA,. 217 first bulged out a little and then gradually pierced through, so that the extremities of the hyphae project above the surface (ZB, ~). The young perithecium has - meanwhile become egg-shaped, its broader portion lying in the medulla being the future basal part, while the narrow end which is wedged into the rind is the future neck with the ostiole. The canal lined with periphyses is formed at an early period in the median line of the neck in a way which has not been exactly ascertained, and the elements at its circumference become thick-walled and black, and hence the neck is soon surrounded by a black outer wall which is con- tinuous with the cortex (7). The process of turning black progresses very slowly towards the base of the perithecium and is only completed when the perithecium is ripe. After the origin of the neck the basal portion of the perithecium ‘extends itself further into the medulla. Its circumference is all the time occupied by a layer of slender firmly woven hyphae running parallel to its surface, and this layer is the outer wall, which also becomes afterwards thick and black. This encloses a tangled mass of filaments filling the whole inner space; the component hyphae, with the exception of the large cells just mentioned, remain delicate and slender and swell strongly in water. The following is the result of Fisch’s investigation into the further development. The peripheral portion of the delicate hyphal weft last-named takes an active part in the further growth, and developes into the thin-walled hyaline pseudo- parenchymatous inner wall or subhymenial layer, which is about 6-8 layers of cells in thickness. The whole of the inner surface of the wall gives rise to slender hyaline large-celled paraphyses which appear at first singly but are afterwards closely crowded together and converge towards the middle having walls that can swell gelatinously, and also to small-celled ascogenous hyphae abundantly supplied with protoplasm, which stand between the points of insertion of the paraphyses and are everywhere in connection with the elements of the subhymenial layer. These hyphae do not reach their full development till the inner space is quite filled with paraphyses, and they develope at the cost of them. With the beginning of the formation of paraphyses, and in proportion as it advances, the primordial tissue, or as much of it as has not been expended on the construction of the inner wall, becomes spongy and gelatinous, and then dissolves and the paraphyses take its place. The same thing happens also to the coil of large- celled tissue which was merely alluded to above and must now be noticed again. In its very early state, in which it was first mentioned above, it may often be easily recognised as one simple row of comparatively large cylindrical cells very full of protoplasm and irregularly rolled up together. In some cases it is uncertain whether it is composed of one or more than one row of cells. It has an exact resemblance, especially in the first case, to the ascogonium of Polystigma, but with this difference, that it is always entirely inclosed in the spherical primordium, and does not send out a trichogyne-process outside it. It takes no direct part in the formation of the asci but, as the primordium increases in size, its coils are drawn asunder and then separated into pieces by the intrusion between them of branches of the transitory primordial hyphal weft.. The entire coil remains inclosed in this weft and swells into a jelly and is dissolved with it; it is rare to see small portions of it taken up by the subhymenial layer and withdrawn from their inevitable fate. The transverse walls in the cells of the coil resist the dissolving influences longest, and even swell for a time into highly 218 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI, refringent plates like those of the trichogyne of Collema; but at length they entirely disappear, the last remains being still recognisable as the paraphyses begin to form. From Fiiisting’s* many researches it is more than probable that the development of the perithecia inside the stroma, not only in all the species of Xylaria and in Ustulina where I observed it some time ago, but also in the genera Diatrype, Stictosphaeria, Eutypa, Nummularia, Quaternaria, and Hypoxylon, runs essentially the same course as has now been described in Xylaria polymorpha, with the exception of course of specific differences of shape and especially of the formation of the wall and the orifice. In all cases there appears, especially in the delicate coil of hyphae which forms the primordium, the row of broad cells irregularly rolled up and full of protoplasm, which Fiiisting terms Woronin’s hypha; in all cases Fiiisting observed the gradual disappearance of these cells without being able to prove a direct connection between them and the ascogenous hyphae, which sprang finally with the paraphyses from the wall of the perithecium in similar relations to them of place and time as in Xylaria. It is true that the views and objects of-observers have so far changed since his in- vestigations that his statements cannot be regarded as certainly infallible, and fresh examination might not be superfluous. 12. The sporocarps of Sclerotinia Sclerotiorum, the conformation of which was shortly described on page 52 (see Fig. 106), show, as the cup begins to expand, the first asci between previously formed paraphyses, and new paraphyses are added one after another with the growth of the margin of the cup, and then more asci are interposed between them, at first singly, but afterwards in greater num- bers and crowd out the paraphyses. Asci and paraphyses are of course branches or the extremities of branches of the hyphae of which the original bundle was com- posed ; but the asci when once found cannot be referred back with the paraphyses to _ common parent hyphae ; only hyphae are found, as Brefeld also states *, which terminate either in paraphyses or in numerous asci; the latter hyphae penetrate deep into the subhymenial layer. In this layer the ascogenous hyphae cannot be distinguished from the others, and where their first origin is to be found, remains uncertain. The examina- tion of the first beginning of the cup in the sclerotium leads to a conjecture on the subject. Certain bodies are formed in sclerotia, if kept moist, before there is any external appearance of sporocarps. ‘These bodies, which here too may be termed primordia (Fig. 104), appear in large numbers in the periphery of the sclero- tium, either close beneath the black rind or a little further in, as round trans- parent objects about 70-100 uw in diameter. They consist of a coil of very narrow tangled hyphal branches with gelatinous membranes; their cavities, which are filled with protoplasm, appear to run through a homogeneous jelly. They originate in single stout medullary hyphae of the sclerotium which are not distinguished from the rest in any other way; branches from these hyphae form the coil of filaments, and its development is accompanied with displacement and gelatinous disorganisation of the adjacent medullary hyphae. The bundle of hyphae of which a cup is formed always bursts from the sclerotium above a primordium of this kind (Fig. 105), and consists of a smaller central portion which branches off directly from the primordium, and a larger 1 Bot. Ztg. 1867. ? Schimmelpilze, IV. CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES.—SCLEROTINIA. 21 9 peripheral mass the elements of which originate in the periphery of the primordium as branches of the stout medullary hyphae. The small central bundle is short, the peripheral hyphae are longer in proportion as they are nearer to the circumference, and, like the periphyses of the Pyrenomycetes, their extremities converge towards the median line, and thus a narrow depression is formed at the apex of the whole which has been noticed before on page 52. No other decided difference of structure isto be observed even at this time between the two kinds of hyphae, and during the subsequent growth FIG. 104. Sclerotinia Sclerotiorum, Thin ver- tical section through the periphery of a sclero- tium which has been kept moist and is ready FIG. 105. Sclerotinia Sclerotiorum. Mediansection through a to develope; beneath the black rind is the young sporocarp which is bursting through the rind. Magn. go primordium of a sporocarp. The dark angular times, but completed from higher enlargements. bodiesare calcium oxalate. Magn 150 times, See also Fig. 14. of the whole body all possibility of distinguishing them ceases. But it is not improbable that the difference reappears with the formation of the ascus, in other words, that the hyphae which have proceeded from the primordium are the ascogenous hyphae and the primordium is therefore an ascogonium, while the erivelope-apparatus of the sporocarp with the paraphyses comes from the peripheral hyphae; and thus the young sporocarp contains from the first the two elements side by side, though they are not anatomically different. The original structure of the primordium is obscured after the emergence of the sporocarp, but its place usually continues to be distinctly marked by the brown colour of the walls of the medullary cells at its circumference; this however may often ultimately spread to the primordium also. The number of primordia in a sclerotium is always much larger than that of the sporocarps which are matured; many are obliterated by their peripheral cells turning brown or are destroyed by the emergence of neighbouring sporocarps. FIG. 106. Sclerotinia Sclerotiorum. Sclerotinia Fuckeliana shows phenomena of fete we ign, borocarps of development quite similar to those which have been described; but there is one difference which adds greatly to the difficulty of obser- vation: the primordia are not formed inside, but on the surface of the sclerotium. A thin bundle of hyphae from the medullary tissue bursts through the rind and developes on its outer surface into a dense round coil, the central part of which is like the primordium of S. Sclerotiorum and is surrounded by the peripheral hyphae 220 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. as a large-celled envelope. The round coil then developes into the at first cylin- drical sporocarp by the aid of branches from the primordium and from its envelope, which have the same relation therefore to each other in this respect as the primordium and medulla in S. Sclerotiorum. The incipient sporocarp is therefore now seated on the rind of the sclerotium in the same form as the one represented in Fig. 105 beneath it. Meanwhile more branches from the elements of the medulla have grown through the rind up to the envelope, so that the rind is pierced by a strand of hyphae as broad as the sporocarp and passing into the envelope, a condition of things which continues in the form represented in Fig. .19. What- ever could be observed of the final maturing of the sporocarp is the same as in S. Sclerotiorum. 13. According to Gibelli’s and Griffini’s researches confirmed by Bauke the development of the perithecium in Pleospora herbarum differs to some extent from those described above, the perithecium being formed by differentiation at a late périod of growth of a spherical primordium originally composed of a uniform pseudo- parenchyma. This arises from one or two adjacent mycelial cells which are converted into the spherical primordium by active cell-division in every direction. The initial cell was previously constituted by one, rarely several, hyphal branches, which show no fixed arrangement and no peculiar changes in their further development. Then a bundle. of slender paraphyses springs from the basal region into the parenchy- matous body, displacing and dissolving its original central tissue, and grows on into the inner space; and after that, in the observed cases after a winter’s rest, the asci are formed ‘in the middle of the paraphyses as branches from their basal cells;’ the’ paraphyses swell into a jelly and disappear as the asci mature. Similar proceedings are perhaps to be observed in Sphaerella Plantaginis ac- cording to Sollman’s statements', but these are not to be relied upon. 14. In Claviceps purpurea, according to Fisch, the formation of the perithecia’ begins with the differentiation of a few cells in the periphery of the young capitate end. of the stroma which proceeds from the sclerotium (see page 38 and also section LXV). Two or three hyphal cells become filled with strongly refractive protoplasm and begin to form by divisions in all directions a very small roundish or elongate-ellipsoid cellular body, which is clearly distinguished from the pseudo-parenchyma of the’ capitulum by the small size of its cells and the nature of their contents. The mode of formation of the cavity of the perithecium could not be certainly ascertained ; but in all probability it is effected by the mutual separation of the cells in the interior, either by the simple parting of the walls or by dissolution of a cell-layer ; in this way a cavity would be formed, the roof of which would be the greater portion of the wall of the perithecium, and its floor become the incipient hymenium. The young peri- thecium as a whole soon acquires the form of an elongated cone by growth in the direc- tion of the radius of the capitulum, and this change is accompanied by an elongation of the whole peripheral cell-layers of the body, thus plainly delimiting the wall of the perithecium. The point of the young perithecium elongates above into a cone, and forms a canal which is beset all round from below upwards with periphyses, while small protuberances grow out of the upper cell-layers of the young hymenium and lengthen. ' Bot. Ztg. 1864, p. 281. CHAPTER V.—COMPARATIVE REVIEW,.—-ASCOMYCETES.—-SPHYRIDIUM. 221 and form asci. No paraphyses are formed. The whole process shows great simi- larity with that described by Bauke in Pleospora. The formation of the perithecia in the stroma of Epichloé is undoubtedly very like that of Claviceps; so probably, according to Fisch, is the same process in Cordyceps (C. militaris, C. ophioglossoides, and C. capitata). The perithecia also of Nectria, according to Janowitsch’s earlier observations and of Cucurbitaria according to Bauke’s report, are formed without initial archicarps, antheridia, or spermatia, but simply by late differentiation of portions of the stroma which were at first uniformly parenchymatous or consisted of closely woven hyphae; in both genera there is also a dissolution of the original central pseudo-parenchyma to make the inner cavity and a formation of paraphyses between the asci. But these older investigations require to be repeated at the present day. R. Hartig’s account of Nectria mentioned above (page 217) is specially deserving of attention ; he suspects that the perithecia in N. ditissima are produced from archicarps which are formed originally superficially on the stroma under a covering of gonidia-forming hyphae, and are then inclosed by branches from adjacent hyphae, and that in conjunction with these latter hyphae they then give rise to the primordial pseudo-parenchymatous formations from which Janowitsch’s investigation sets out. The possibility of similar processes is not entirely excluded by the accounts which we possess in the case also of Epichloé. 15. Van Tieghem gives the name of Ascodesmis to two small Dincdinj notte which in the full-grown state look like small Ascoboli and are distinguished by reticulate thickenings of their spore-membranes. He describes the development of their apothecia from specimens cultivated on microscope-slides in the following manner. A slightly bent lateral branch rises from a cell of a filament of the mycelium, and, after a short increase in length, branches in a pseudo-dichotomous manner ; this mode of branching is repeated through several orders in planes which intersect each other alternately, and the successive branches have a similar curvature. At length they all become woven together into a cushion of compact pseudo-parenchyma, which is attached on. one side to the mycelial filament by a short stalk. Then closely crowded paraphyses shoot out from the superficial cells on the opposite side, and then the asci one after another from the same surface and between the paraphyses. We are not told whether any difference appears between the ascogenous cells and those which form paraphyses, or if the asci at least which follow one another spring from distinct ascogenous hyphal branchlets. 16. The apothecia of Sphyridium fungiforme, 8S. placophyllum and Cladonia Papillaria consist in the mature state of close-set paraphyses and of asci inserted between them, and the asci arise from distinct ascogenous hyphae in the hypothecium. According to Krabbe* the commencements of these apothecia are peripheral shoots from the outer surface of the thallus, and the layer of paraphyses first makes its appearance and afterwards the ascogenous hyphae with the asci. No trace was observed of a distinct carpogonium or archicarp, as the source of the ascogenous hyphae, or of any co-operation of spermatia; on the contrary, the ascogenous hyphae are branches of ‘ordinary’ hyphae, hyphae, that is to say, which are not distinguishable from vegetative hyphae and from those which form 1 Bot. Ztg. 1882. 222 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI, paraphyses. The sporocarps of Baeomyces roseus, which are very like those of Sphyridium in shape, first appear as coils of hyphae in the interior and deep beneath the surface of the thallus, and are there differentiated into layers of paraphyses and ascogenous hyphae. Subsequently they emerge from the thallus as long-stalked bodies in consequence of the elongation of their basal portions. But Krabbe was unable to arrive at any more positive conclusion with respect to the origin of the ascogenous hyphae than in the case of Sphyridium. According to the same observer Sphyridium carneum exhibits a curious variation from the genera with which it has hitherto been associated. Its sporocarps would appear to be only pseudo- sporocarps, sporocarp-like shoots from the thallus, which form neither paraphyses, nor asci, nor even spores, only coils of hyphae beneath the surface, in appearance like the ascogenous hyphae of allied species, but never forming asci. We learn from Krabbe’s latest ‘ preliminary’ communication that in the Clado- nieae, except Cladonia Papillaria, the whole of the large body known in descriptions as podetium, for instance the well-known cup in C. pyxidata and the branching shrubby form in C. rangiferina, is by its mode of origination an apothecium. . It is formed as a primordial hyphal coil in the interior of a crustaceous or foliaceous thallus and forces its way through the rind outwards and then arrives by progressive or inter- calary growth at its final form. The differentiations into ascogenous hyphae, dis- tinguishable from the rest by turning blue with iodine, and the paraphyses is effected without a distinct archicarp and virtually in the same way as in the species of Sphyridium and Cladonia already. mentioned; taking place either when the body is just emerging from the thallus, as in C. decorticata, or not till it has acquired in separate parts the final cup-like or shrubby form. Ascogenous hyphae and even asci may in some species revert to the vegetative form, and certain kinds which have paraphyses in the normal manner either do not produce perfect asci, or only do so exceptionally. We must wait for the author’s more detailed accounts, and we shall return to the anatomical character of the podetium in section CXVI. ' From the agreement found among the sporocarps of the Ascomycetes in the mature state, it may be considered to be certain that they may all be included as respects their origin in one or other of the types above described or come very near them; which type it should be must be inquired into in each particular case, and cannot be decided with certainty from the mature condition. The many careful researches of Schwendener and Fiiisting into the formation of sporocarps in Lichens may still be adduced in support of this view; these observers failed to account for the first beginnings only of the ascogenous hyphae which are differentiated at a very early period. Fiiisting reports the presence of Woronin’s hypha in the young sporo- carp of Lecidea formosa, and Stahl’ says of Parmelia stellaris and P. pulverulenta and Endocarpon miniatum:; ‘It is not difficult, especially in layers of Parmelia stellaris with many sporocarps, to find the extremely delicate apex of the trichogyne in young sporocarps; I succeeded in some successful preparations in showing the connection between these processes and the ascogonia which were distinguished by the abundance of their protoplasm.’ Since spermogonia and spermatia are present in all these forms, as they are in the Collemeae, it is natural to suppose that there is a near agreement between them and the Collemeae ; but this is not yet demonstrated. Fiiisting says that he has not found his Woronin’s hypha in species of Verrucaria, ’ Beitr. z. Entw. d. Flechten, p. 41. CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES. 223 Pyrenula, and Polyblastia, and Krabbe’s results given above make it highly probable that the processes in the Lichen-fungi with which he was dealing are of a different kind. With regard to the rest of the phenomena observed in the sporocarps of the Lichens of which we are speaking, it may be remarked that apothecia as well as peri- thecia are not formed on the surface as in Collema and most of Krabbe’s species, but inside the thallus, as in Xylaria, in the shape of coils of delicate primordial hyphae which only come to the surface in the course of further development, pushing aside the tissue of the thallus above them in a manner which varies with the species. In species of Placodium, Lecanora, Zeora, Callopisma, Lecidea, Blastenia, Bacidia, and Pannaria, which have been examined and which form apothecia, a dense tuft of slender branched filaments, growing towards the outside, shoots out at an early period from ‘ the whole of the upper side of the primordial coil which is turned towards the upper surface of the thallus; these filaments are the first paraphyses. An outermost layer of | similar filaments, open above and of varying thickness in each case, surrounds the tuft of paraphyses and runs tothe surface of the primordial coil; this layer is the excipulum, though not exactly in the sense in which that word has been used hitherto in descriptive Lichenology. The excipulum is either formed at the same time as the first paraphyses, so that the outermost rows of the tuft become the hyphae of the excipulum, as in Placodium, Lecanora, Lecidea, &c., or before the paraphyses as in Blastenia ferruginea, Huds. according to Fiiisting. While the filaments of the primary tuft of paraphyses increase in length and form new branches, which insert themselves vertically between the first ones, and while the excipulum enlarges its surface in every direction by the formation of new interposed hyphae and grows by the appearance of new elements at its margin and of new hyphal branches continually behind the margin, which are like the primary paraphyses and in contact with them on the outside,—while all these processes are going on simultaneously, the young sporocarp by accession of new elements increases in height and thickness. The introduction of new branches - continues for some time in the lower portion of the original tuft of paraphyses, and in such a manner that the filaments which were at first parallel become irregularly woven together, forming a tissue which cannot be distinguished from the primordial coil. The formation of new elements is followed directly by increase of size through expansion of the previous elements. The whole growth is first completed in the middle of the sporocarp; it continues longest, and often a long time after the sporocarp has appeared on the surface of the thallus, in the upper margin of the .excipulum and close underneath it, where new constituents are being constantly and progressively added by apposition. The ascogenous hyphae also make their appearance with the first paraphyses. The formation of the perithecia in Lichens from the primordial coils of hyphae follows in general the same course as that which has been given for Xylaria and Polystigma, &c.; but the first origin of the ascogenous hyphae is unknown. Peculiar features and deviations from rule may be studied in the authors named above, especially Krabbe and Fiiisting. CouRSE OF DEVELOPMENT OF THE ASCOMYCETES. Srction LXV. The life-history of the Ascomycetes has been thoroughly studied in the same species as the development of the sporocarps; there are many besides in which it is sufficiently known to allow of our comparing them with the others and judging of them with certainty. The simplest case is where under normal conditions the germinating spore developes directly a mycelium or thallus, which also directly produces sporocarps in the modes described above, without the appearance of any other organs of 224 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. propagation not belonging to the sporocarp. This is the case in Eremascus albus, Hypocopra fimicola, Ascobolus furfuraceus, Pyronema, Gymnoascus, species of Collema, Endocarpum pusillum, Thelidium minutulum, and very many, if not all, Lichen-fungi; a similar course of development is the almost invariable rule in Sclerotinia Sclerotiorum, where a filamentous mycelium grows from the germ-tube of the spore, the mycelium producing sclerotia and the sclerotia sporocarps. Single resting-cells, which occur accidentally in the mycelia and then resume active growth, are no more to be taken into consideration in this connection than the soredia of Lichens which will be described in section CXVII. More distinct formations of gonidia have not been observed in this course of development. There is a second case in which the development may proceed as in the first ; but it commonly happens that a formation of distinct gonidia is introduced, and the products of their germination resemble those of the ascospores. A good example of this kind is to be found in Sclerotinia Fuckeliana’. A primary mycelium grows from the germinating ascospore, and may in the simplest case produce sporocarps directly and without going through any intermediate state. I have observed this once and in one specimen only cultivated artificially in grape-juice on a microscopic slide. The sporocarp was produced directly from a tuft of mycelial branches resembling in appearance the primordium of a sclerotium, but its initial states were not further examined. The general rule is that sclerotia are formed (p. 34) on the primary mycelium; then either sporocarps alone proceed from the sclerotium, as in Peziza Sclerotiorum, or filamentous gonidiophores, which are known under the name of Botrytis cinerea, Pers. One only of the two forms appears on a sclerotium, never both together or one after the other. These gonidiophores may also grow directly from the mycelium which has proceeded from ascospores, without prejudice to future formation of sclerotia, but this certainly does not very often occur. Finally, the germinating gonidia produce a mycelium with all the characteristics of one that has proceeded from the ascospore and giving rise to the same products, but with this difference that it inclines much more to the formation of gonidiophores. To ° these phenomena is to be added the occasional formation of special abortive gonidia or doubtful spermatia, which must however be noticed again in section LXXIV. A third case is that of a number of species in which it must be allowed that the course. of development proper to the first category is possib/e, but is never actually observed. More usually the primary mycelium or thallus formed from the ascospore always produces gonidia. Strictly speaking, two subdivisions may here be dis- tinguished :— a. The primary mycelium which proceeds directly from the ascospore is reduced to a promycelium (section XXXI) which produces sporidia; these give rise to the definitive thallus, which then behaves as in the first category or as in the cases placed under 4 Of this kind is Polystigma rubrum and Rhytisma Andromedae also, to judge from the germination of the ascospores. In this case also the formation of gonidia is as a rule a necessary part of the development, for a perfect fertile thallus is not produced without its interposition. 1 See Pirotta in N. Giorn. Bot. Ital. XIII, p. 130. CHAPTER V.—COMPARATIVE REVIEW.---ASCOMYCETES. 225 4. A richly vegetating primary mycelium or thallus proceeds from the ascospore, and its complete development closes with the formation of sporocarps, but as a matter of fact it always first produces gonidiophores with gonidia. The germinating gonidia again give rise in all cases to a mycelium or thallus of the same qualities and capabilities as those which sprang from the ascospore. Here therefore the formation of gonidia is not necessary to the development, but it is, as a matter of fact, an invariable occurrence. It precedes the formation of sporocarps in the history of the individual, and the gonidiophores were therefore often termed the precursors of the sporocarps. The formation of gonidia is usually extremely copious in this third category, often much more copious than that of the sporocarps, and then generally owing to external causes which can be demonstrated; it may be the only mode in which the species is propagated during many successive generations, while sporocarps appear exceptionally and under special conditions. Some species have more than one kind of gonidia, which may then be distinguished according to size as mcro- gonidia, megalogonidia, macrogonidia, or by special names in particular cases according to other characters. ‘ Again, the gonidia are formed in certain cases on the free surface of the thallus on single hyphae or in crowded hymenia; or else in receptacles resembling perithecia. These latter have been termed by Tulasne pycnidia, and the spores or gonidia formed in them stfylospores—not very happy expressions; the first, however, may be retained here, the latter replaced by the words pycnospores or pyenogonidia. All known gonidia in the Ascomycetes are acrogenously abjointed after one or other of the forms described in section XVI, and none are swarm-cells. Examples of species which have been fully examined. The germinating ascospore in the Erysipheae (Fig. 107) puts out a short germ-tube, which on a suitable substratum, namely the living epidermis of certain Phanerogams, sends first of all a haustorium (Fig. 6) into a cell of the epidermis, and then developes into the filamentous branched thallus which spreads over the whole surface. Short erect branches of this thallus then serially and successively abjoint large colourless cylindrico-ellipsoid gonidia, and each of these gonidia yields in germination under favourable conditions the same product as the ascospore. Every thallus which proceeds from these germinations ends, when it has reached its full development, with the production of archicarps and antheridia, that is, of sporocarps. But it need not always arrive at this conclusion, but may only form gonidia and propagate itself by means of them through an unlimited number of generations. This imperfect development may usually be traced to obvious external causes, such as climatic conditions or the absence of the nutrient substance required for perfect development, that is, the proper species of Phanerogam. The Erysiphe of the grape-vine is the best example of the group’. From the circumstances attending its first appearance and its diffusion in Europe, it may be safely assumed that it suddenly migrated, and was transferred to our vines from some other species of Phanerogam. It most probably came from America. In spite of its destructive diffusion over the whole of wine-growing Europe the most careful examination has never detected any sign of a sporocarp; the invasion was, entirely carried out by vast numbers of gonidia, the shape of which procured the plant the name of Oidium (O. Tuckeri, Brk.). The sporocarps are probably found in N. America on native species of Vitis and described as Erysiphe (Uncinula) spiralis, Brk. and Curt., but this is not certain. ? Beitr. z. Morph. u. Phys. d. Pilze, III, p. 50. L4] Q 226 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI, The course of development in Eurotium and Penicillium may be described in the same words as in Erysiphe, making allowance for differences of form and for the circumstance that the species in the two last genera are not epiphytic parasites, but (for the most part) inhabit dead organic bodies ; here too we find frequent absence of sporocarps where the vegetative conditions are not altogether favourable. The gonidiophores of Eurotium (Figs. 94 and 35 4) are erect usually unicellular hyphal branches inflated and bladder-like at the apex, where closely crowded radiating sterigmata of uniform height are developed, and from these sterigmata spores are serially and successively abjointed. The gonidiophores in Penicillium (Fig. 36) are narrowly filiform, septate, and cymosely branched, and at their extremities, which are erect parallel and close to one another and terminate at nearly the same height, spores are formed by serial successive abjunction. The sporocarps of Penicillium glaucum have at present been found only in dark or imperfectly lighted places where the supply of oxygen is small, and chiefly on bread (Brefeld) ; I myself found them in abundance on a heap of grape-skins, both growing naturally and after the spores had been sown by hand. FIG. 107. J, 1] Podosphaera pannosa. J chain of gonidia on the gonidiophore and mycelium, // ripe sporocarp ; the ascus a is emerging through the wall of the sporocarp # which has been ruptured by pressure. ///—V Podosphaera Cas- tagnet. JII archicarp ¢ with antheridial branch # on the mycelium, /V older state; ¢ archicarp invested by the hyphal branches of the wall, g antheridial branch. V still older state in optical longitudinal section; @ ascus with its pedicel- cell, the product of ¢, # the wall. J, // after Tulasne. Magn. 600 times. The course of development of Melanospora parasitica again is on the whole very like that of the above species, except that the gonidiophores—short verticillately branched hyphae with whorls of secondary branches, from which spores are acro- genously and serially abjointed—are very rarely produced, the work of propagation falling chiefly to the ascospores. The peculiar parasitism of this Fungus will be considered in Chapter VII. The ellipsoidal ascospores of Polystigma rubrum ripen in spring. They put out a_short tube on a moist substratum, and the extremity of the tube, which also swells into an irregularly ellipsoidal form, receives the whole of the protoplasm, and is then abjointed and forms a thick-walled spore-cell (gonidium, sporidium). This cell readily germinates on a moist substratum,and on the epidermis of a foliage-leaf of Prunus the germ-tube penetrates at once into the nearest cell and there puts out branches, which then grow rapidly through the wall of the cell into the parenchyma of the leaf. Here they grow at the cost of the tissue of the leaf and displace its elements, but always covered by the epidermis, ahd in a few weeks’ time they have \ CHAPTER V.—COMPARATIVE REVIEW,—ASCOMYCETES, 227 formed closely woven thallus-structures (see page 43), which cause roundish red spots about I cm. in diameter in the still living green leaf; spermogonia and archicarps make their appearance in the spots in the course of the summer. The Fungus does not go beyond the complete development and subsequent fertilisation of the archicarps during the summer, but falls to the ground in autumn with the leaf, and there the further development of the perithecium takes place, if the conditions are favourable, at the expense of the reserve of food in the thallus ; the spores become ripe in the ensuing spring. The process can of course be to some extent hastened or retarded in plants under artificial cultivation by changes in the temperature and in the supply of moisture. The sclerotia of Claviceps purpurea and its nearest allies (see section VIII) mature during the summer and remain dormant all the winter; in the next spring each Oy of) WIR Te. la aN’ in Wal’ nN Ny ain Co fi Dh ‘ ae AM ASN FIG. 108. Claviceps purpurea, Tul. A sclerotium which has given rise to seven FIG. 109. Claviceps purpurea, stromata. B upper portion of a stroma in median longitudinal section ; cf perithecia. Tul. Ascospores germinating 48 C highly magnified perithecium divided through the middle with the surrounding hours after being scattered on parts ; ¢f orifice, s# cortical tissue, Xy inner tissue of the stroma. D ascus isolated; sf water. Magn. 375 times. — ascospores issuing. After Tulasne from Sachs’ Lehrbuch. J natural size. A slightly, C and D highly magnified. sclerotium, ifit happens to lie on moist ground, usually produces several spherical stalked stromata (Fig. 108 A), the upper spherical portion of which is thickly covered with perithecia sunk half-way beneath the surface (B, C). The ejected cylindrical filiform ascospores (2) swell in different parts under the influence of moisture, and put out germ-tubes at several points (Fig. 109). If the ascospores of Claviceps have found their way into young flowers of the Gramineae (Secale in artificial cultivations) under conditions favourable to germination, their development begins in the pistil, according to Kiihn’s observations, and doubtless after the germ-tubes have penetrated into the pistil, though this has never been directly observed. The young pistil concealed between the paleae is first of all traversed in every direction and enveloped by a luxuriant growth of the hyphae of the Fungus, as has been already described : a white hymenium, Léveillé’s Sphacelia, then forms on the whole of the furrowed surface, and from cylindrical sterigmata on it gonidia are abscised (Figs. 110, 111 a). During the formation of Q 2 228 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI, the hymenium the well-known saccharine fluid is secreted, which oozes out from between the paleae in thick drops rendered turbid by count- less gonidia, and thus betrays the presence of the parasite. This juice is eagerly sought by in- sects, which thus carry away the gonidia. Soon the formation of the scle- rotium begins in the basal portion of the gonidia- forming body in the way already described. The sclerotium reaches matu- rity by the time that the grass’is ripe and passes into the dormant state which lasts till the next spring. The gonidia readily put out germ- tubes as soon as they become free, and the tubes sometimes produce small — upright branches on the microscope- slide, from which fresh gonidia are then abscised (Fig. 111 4). Kiihn informs us that new gonidiophores and _ scle- FIG. 110. Claviceps purpurea, Tul. Portion of athin longitudinal section onthe boundary yotia are developed in the line between the gonidiophore ss—cc and the young sclerotium #. See Fig. 17. After Tulasne, from Liirssen’s Handbuch, highly magnified. manner described above from the germ-tubes of gonidia, which have found their way to the flowers of a grass. Nectria ditissima may be given from R. Hartig’s description? as an example of FIG. 111. Claviceps purpurea, Tul. a thin transverse section through the layer from which gonidia are being abscised, 4 gonidia germinating and producing by abjunction a small group of secondary gonidia at x. a@ after Tulasne, highly magnified, 4 after Kiihn. a species furnished with more than one kind of gonidium. The mycelium lives in the rind of leafy trees, and causes the disease known as ‘canker.’ It forms a small cushion-like pseudo-parenchymatous thallus beneath the surface of the rind; the thallus eventually bursts through the rind and produces first gonidia and then perithecia on its outer surface. A sufficient account has already been given of the perithecia, which in the ptimordial state are concealed beneath the gonidia and the structures producing them, but these are displaced and thrust aside by the perithecia. The gonidia are now formed acrogenously outside the cushion on short slender filiform sterigmata arranged side by side and parallel to one another, so as to ? Unters. a. d. forstbot. Instit. Miinchen, 1. See also Tulasne, Carp. III, and R, Gothe, Der Krebs d. Apfelbaume in Thiel’s Landw. Jahrb. IX (1880). CHAPTER V.—COMPARATIVE REVIEW,-—ASCOMYCETES. 229 produce a dense hymenium. The gonidia in the highest state of development are abjointed successively in long rows forming a close colourless mass which covers the cushion, each gonidium having the form of a bent cylinder 60 » in length and divided by transverse walls into several members (spore-cells), which may be as many as eight in number. Besides these there are some much smaller, but of similar origin, in which the number of members sinks to two. Each segment-cell of these gonidia may develope in a moist atmosphere into a branched hypha, from single branches of which fresh smaller gonidia are abjointed. If the mycelium vegetating in the tissue of the rind of the tree comes to lie exposed in a moist atmosphere, it sends out numerous branches into the air, and from these also countless small gonidia are abjointed. The size of all these small gonidia sinks by regular gradations to 1.5 y; they are all cylindrical and rod-like; those of medium size are divided by a transverse wall into two segments which often separate from one another; the smallest are undivided. All down to the size of 2 » can put out germ-tubes or may also multiply by sprouting. The very smallest have never been observed to put out germ-tubes, but they appear to multiply by division and fission and by sprouting. Lastly, gonidia of the smallest kind are also formed in great numbers by slender branches of the mycelium in the interior of the tissue attacked by the Fungus. All germ-tubes, whether from gonidia or from asco- spores, can develope new fertile mycelia in the proper substratum, that is, in the living rind of a tree; it is doubtful whether the smallest gonidia can produce mycelia (see section LXXIV). There is also some doubt as to the true nature of certain acro- genously abjointed spores which occur on the sporocarp-bearing portions of the Fungus which we are considering; they appear to belong to parasites of Nectria, and it will be sufficient therefore in this place to refer the reader to Hartig and Tulasne. The development of Cordyceps with its great variety of forms will be described subsequently in Division III. The cycle of development of the one or perhaps two species included under the name of Pleospora herbarum is particularly rich in forms. These are found in dead and rotting herbaceous plants. The results which will be given here were obtained from plants cultivated in nutrient solutions on the microscopic slide. The mycelium forms (1) the Jerithecia mentioned above with pluricellular compound ascospores : (2) gonidia of three kinds produced acrogenously on filiform gonidiophores, namely,— (a) bicellular or-pluricellular spores resembling the ascospores, in general shape shortly cylindrical to roundish, with dark-brown thick membranes rough with fine points on the outside, named by Berkeley as a form-species in 1838 Macrosporium Sarcinula and therefore called by Gibelli and Griffini the Sarcinula-form ; they are usually produced singly at the end of the gonidiophore ; (4) the Alternaria-form, classed with the old form-genera Alternaria, Sporidesmium, Mystrosporium, and Polydesmus ; these are coni- cally pear-shaped pluricellular compound spores having a smooth light-brown membrane, and arising at the extremities of the hyphae in long and often branched rows (Fig. 34) ; (c) a form said by Bauke to be a microgonidial form, but of which he gives no further description; it is not the one known as Cladosporium herbarum and placed by Tulasne with Pleospora herbarum, for this, according to all later investigations, does not belong to this place at all and its genetic connection is uncertain: (3) pycnidia (see below, section LXXI, Figs. 118, 119) which appear as intercalary formations on branches of the mycelium. A piece of the hypha consisting of one or several cells swells in the same way as when a perithecium begins to be formed, and its cells divide at the same time meristematically and irregularly by walls inclined in every direction. By this process of growth a small-celled parenchymatous body is formed of many layers, which is round or irregularly elongated in shape and seldom more than 0.2 mm. in size, often much less. This body is at first uniformly dense, but towards the end of its growth a central cavity is formed in it surrounded by the many- layered wall ; this cavity is produced by the cells of the central part ceasing to follow the growth of the outer parts in the direction of the surface and therefore separating 230 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI. from them. The cell-rows which bound the cavity project into it from the first with radial convergence, and fresh ones are formed resembling these and between them. The wall of the cavity is thus lined with slender converging rows of short cells, which begin at once to form numerous fycnospores terminally and laterally on all their cells by successive abjunction. These spores are elongate-cylindrical, very thin-walled, 2.8-4 in length and about half that breadth, and are surrounded by a hyaline gelatinous or gum-like substance, perhaps the outer wall-layer. Imbedded in this gelatinous envelope they are heaped up in large numbers in the interior of the pycnidium. When their formation begins the outer wall-layer of the pycnidium, which has hitherto been colourless, is thickened and becomes brown. At the same time a narrow opening is formed in the wall usually at one, rarely at more than one, place by the retreat of the cells from one another, and the orifice is usually surrounded on the outside by a circle of projecting cells like short papillae. In this state the pycnidium has reached its full development ; addition of water causes violent swélling of the mucilage which envelopes the spores, so that they collect into a gelatinous mass and are squeezed out of the narrow opening in countless numbers, forming a tendril-like body or a round gelatinous drop according to the degree of moisture ; they separate at once in water. All the vegetative cells of this Fungus and its allied forms show a tendency to form thick brown membranes like those of the perithecia, pycnidia, and gonidia. With these walls they can pass eventually into a long period of rest and return from it under favourable conditions to vegetative activity and the formation of spores. These resting mycelia, and detached single cells or portions of hyphae (gemmae), may appear in numbers at the close of their culture and add to the variety of forms. . As regards the genetic relations between all these forms, we are only told of the microgonidia, that they occur in company with other gonidial forms. Observers also agree in saying that a mycelium is produced from the germinating ascospore, and can first produce gonidia and then perithecia and pycnidia; it behaves therefore in the same manner as the rest of the gonidia-bearing plants described above as regards the successive formation of organs of propagation, except in the matter of the pycnidia. Gibelli and Griffini saw a mycelium proceed also from the Sarcinula-gonidia, which first produced similar gonidia and then perithecia; sometimes in this case also the mycelium which has grown from the two kinds of gonidia does not proceed beyond the formation of gonidia. But the pycnospores, which swell strongly in a nutrient fluid and even form transverse walls and then put out germ-tubes, produce a mycelium from them which uf ¢o the present time has never borne anything but pycnidia in cultures, even when these have been continued through a large number of generations. It would appear probable that the mycelium could produce perithecia when growing on its natural substratum, but this has not been proved. While observers are agreed up to this point, the views of the Italian botanists differ in other respects from those of Bauke. They are of opinion that two similar but always distinct species are confounded together under the name of Pleospora herbarum, one Pleospora Sarcinulae, which is constantly characterised by the presence of the Sarcinula- gonidia and by larger ascospores, the other Pleospora Alternariae, which as constantly has the Alternaria-form of gonidia. They found pycnidia only in P. Sarcinulae. On the other hand according to Bauke a mycelium proceeds from the ascospores of the same perithecium, which forms ezther pycnidia in company with Alternaria-gonidia or perithecia with the gonidia of P. Sarcinula. The mycelium from each of the gonidial forms always produces gonidia of the same kind as the one from which it proceeded. Further observation must determine which of the two views is correct, but the analogy of other Fungi makes that of the Italian writers the more probable. The decision of this question is not important for our present purpose, because, as was intimated above, in the one case we are dealing with one species with a great variety CHAPTER V.—COMPARATIVE REVIEW,—ASCOMYCETES. 231 of forms, in the other with two species with fewer forms and in other respects like one another. Section LXVI. The remarks which have now been made render it un- necessary to say anything more concerning the homology of members of the same name in the Ascomycetes which we are here considering; nor need we further discuss the fact, that the mature sporocarp contains in some cases only the products of the development of one archicarp, in others, as in Physma and Pyronema, the results of the development of several archicarps, We could if necessary establish sub-forms on this distinction. The question of the homology of the spermatia and spermogonia is not so readily settled; but even here the difficulties are not great. It may be conceded that the consideration of the function of the spermatia of the Collemaceae puts us on the right track. That function, as will be shown in the following section, is the same as that of the antheridia in other and allied species. Hence arises the consideration whether the spermatium with the spermatio- phore, the sterigma, is not the homologue of an antheridial branch from which portions are abjointed in the form of spermatia, according to the arrangements of particular species, in order to be capable of the fertilising function. Forms like Collema, in which spermatia and archicarps are formed at a distance. from one another, may not afford any sure ground for an answer to the question ; but the case is different with Physma, where spermatia and archicarps spring close together from branches of the same hyphal coil, like the antheridia and archicarps of Pyronema. If the spermatia in Physma remained fixed to their spermatiophores in order to conjugate with the archicarp, the only difference between the two forms would be that of conformation. The actual differences, it is true, go farther than this, since the spermatiophores are combined into a spermogonium from which the spermatia are discharged, and the archicarps are outside of it, and send up the trichogyne to the place where it encounters the spermatia. But we can understand all these phenomena as adaptations to suit the origin of the two organs inside a dense thallus which impedes their direct meeting, and still maintain the homology with Pyronema. Even the excessive numbers of the spermatia or antheridial branches will be quite intelligible in view of the very general rule that the number of male sexual cells in a species increases with the difficulties in the attainment of its physiological aim. But homology of the spermogonia and archicarps of Physma. with those of Collema is quite obvious ; the latter agree perfectly with the former in every respect except in their diclinous and monoecious distribution, which in some forms’ inclines to dioecism. But this arrangement is no difficulty in the question before us, since diclinism may appear everywhere and is actually observed in many species, in which sexual cells are endowed with free motion whether active or passive. It follows from these comparisons and considerations that in Collema also the spermatia with their spermatiophores may properly be considered to be homologues of the antheridial branches and antheridia of more simple forms, and the pecu- liarities of their development, and the excessive numbers in which they are produced Stabl, Beitr. z. Entw. d. Flechten, pp. 30, 38. 232 DIVISION II,—-COURSE OF DEVELOPMENT OF FUNGI. in special receptacles, as adaptations to special circumstances of development, the further consequence of which is the establishment of diclinism. It must be admitted that comparisons of this kind are always somewhat insecure and readily afford too much room for the play of fancy, if they are not supported by a more complete series of well-known intermediate forms than can at present be produced in this case. The comparison in the text may be offered with this reservation attached to it. It appears to me to fit in quite naturally with ascertained facts; nor is it too much to expect that the intermediate forms that are wanted will be found, if we consider how few of the whole number of Ascomycetes have been examined up to the present time. : If we compare the whole course of development of the Ascomycetes in which this course is fully known with that of the groups of Fungi described in previous sections, we become distinctly aware of a parallelism between Eremascus and the Ascomycetes, which are provided with archicarps and antheridial branch on the one side, and the Mucorini, Peronosporeae, and Saprolegnieae on the other. A thallus proceeds from the carpospores (ascospores, oospores), and terminates its development with-the formation of an archicarp and antheridial branch and of the new carpospore which is formed from them. To this the whole course of the development is limited in many cases, as in Eremascus, Pyronema, and species of Ascobolus on the one side, and on the other in Pythium vexans and Artotrogus ; in most cases it is interrupted by the formation of other spores, the gonidia. The gonidia of a species are sometimes all of one kind, as in Erysiphe and Peronospora, sometimes of more than one kind in the same species. The parallelism extends even to close resemblance in form in organs of the same name in certain groups. Eremascus might, to judge from Eidam’s description, be almost ranked with the Mucorini, especially the Piptocephalideae ; on the other hand, none of the essential developmental characters of an Ascomycete are wanting in it. In the form of its archicarps it is perfectly like Penicillium, Gymnoascus, Eurotium and other genera. There is also a great amount of agreement in respect of the thallus, formation of the gonidia, archicarp, and antheridial branch between the Erysipheae, especially Podosphaera, on the one hand, and some Peronosporeae on the other’. These groups therefore establish a nearer connection between the Ascomycetes in question and the Peronosporeae; a convergence of the two groups which amounts to actual contact and may be regarded as phylogenetic affinity. This connection with the Peronosporeae is closest in Podosphaera, because there caeferis paribus not only the archicarp and antheridial branch are like the same parts in the Pero- nosporeae, as, for example, in Phytophthora omnivora, but the ultimate develop- ment also of the archicarp only goes a little further; the eight-spored ascus with its stalk proceeds from division of the cell twice repeated, while in Phytophthora the archicarp becomes the oogonium with the oospore. Erysiphe is closely con- nected with Podosphaera, in which the archicarp by repeated cell-division and - branching gives rise to a number of asci, and all the rest of the Ascomycetes in question with Erysiphe, as appears plainly from the details which have been given ' For a more extended comparison see Beitr. IV, p. 109. CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES. 233 above. These comparisons show that archicarps, antheridial branches, and all other parts of the same name in all the Fungi which are here compared, are homologous. The homologies go as far as the archicarp; they cease with its further de- velopment, unless we may perhaps compare the oospore of Cystopus which forms swarm-spores directly in germination (page 135) with: an ascus; the ascus of Podosphaera and Eremascus is an organ which does not appear in the Peronosporeae, and this may be said still more of the sporocarp of Erysiphe and the series of forms which follow it. The series of the Ascomycetes and that of the Mucorini and Peronosporeae set out on divergent routes from Podosphaera and Eremascus, as the members which touch one another in the two series. It must not be forgotten that 2 this comparison of sporocarps, the parts spoken of above as the ascus- apparatus are alone to be taken into consideration, and have been considered here. The envelope-apparatus, important as it isin other connections, does not enter into the question. For the case is exactly the same if there is no envelope-apparatus, as really happens in Eremascus, and would be the same if there were Peronosporeae with their oogonia in envelopes ; this, it is true, has not been observed, but it is quite possible, and in Mucorini (see section XLII) the zygospores are provided with envelope-apparatus of great variety of form. -When once the homology between the archicarps of the two groups is proved, that of all the spores, which have been termed gonidia in the preceding pages, is also established. The expression was anticipated above throughout in the case of the Ascomycetes, so far as it was supposed to have exactly the same meaning as in the Peronosporeae and their nearest allies. In the Peronosporeae the antheridial branch and the> archicarp function as sexual organs. But homologous meméers need not also function in all*cases as exactly similar organs, as appears at once from the case of the Saprolegnieae with doubtful sexuality and with sexuality undoubtedly wanting. Hence when the homology has been established it is still an open question, whether the members of the Ascomycetes in question are sexual organs or not. To understand clearly this much discussed question’ we must first of all remember that, in our imperfect knowledge of the nature of sexuality and the sexual process of fertilisation, . we have no simple mark or reagent by which we can recognise the sexual quality of an organ. We learn from the facts before us that in every process of fertilisation there is a material union of one peculiar male or fertilising cell or at least of a portion of its protoplasmic and nuclear substance with one other, a female cell, which is to be fertilised, or, as in the Florideae, with a pluricellular female apparatus*. The result of this union is that the female portion is rendered capable of further development: the development does not take place without this union, and union with the male portion is necessary that the female may become capable of it. In a doubtful case therefore the determination will depend first on the observation: of the union of the protoplasm or nucleus, and secondly on the experimental proof of the necessity of this in order that the presumed female portion may become 1 See Beitr. IV, pp. 74, 111. We cannot enter here into a discussion of the general question of sexuality; the beginner is referred to Sachs’ Text-book, 2nd Engl. ed. * See the work cited on page 213, and Fr. Schmitz in the Monatsbericht d. Berliner Acad. 1883. 234 DIVISION IIl.— COURSE OF DEVELOPMENT OF FUNGI. capable of development. .We may derive assistance also from analogies of cases which have been certainly ascertained; but these have only a subordinate value, for experience has certainly shown that sexuality is a phenomenon of irregular occurrence in the greater part of the vegetable kingdom, varying sometimes from species to species even in the higher plants, and hence homologies and analogous functions are here also not necessarily coextensive. According to these criteria the sexual organs of Pythium, for example, are really sexual, for the union of protoplasms is evident, and its necessity, though not demonstrable in strictly experimental manner by artificial separation and conjunction of the two parts, is all but absolutely proved by the fact that the union always takes place: but if we apply the same criteria to the homologous organs of the Sapro- legnieae the sexuality will at least be very doubtful. Similar results are obtained by the same method of determination in the case of the Ascomycetes in question. The protoplasms unite in Pyronema, and there is no exception to this rule; and as strict experiment is impossible, we may conclude, as in Pythium, with almost perfect certainty from the constancy of the phenomenon, that the union is necessary. The phenomena in Pyronema _ are so far different from those in Pythium that the archicarp grows to meet the male organ by means of a special organ, the /richogyne, and unites its protoplasm with that of the male organ; this union takes place after the trichogyne has previously been permanently delimited as a special cell by a transverse wall. These facts could hardly be understood but for the exact analogue presented by the majority of the Florideae. But these make it plain that, the trichogyne is an organ of conception which first receives the fertilising matter, and that the effects+ of fertilisation are conveyed from it, in a manner which cannot be further considered here, to other parts of the female apparatus, which in the present case is the ascogonium. We are made acquainted with quite similar phenomena to those in Pyronema, though different certainly in form and more complex, from Stahl’s observations on the Collemaceae which have been described above. The most important complication arises from the fact that the male organs are spermatia detached by abscision, not antheridial cells formed beside the archicarp. The union with the trichogyne and the changes which proceed from the place of conjugation and affect the female apparatus which ultimately forms asci are very apparent. The necessity of the union for the further development of the female apparatus is in this case also not shown by strict experimental proof on account of technical difficulties ; but it is as good as certainly proved by the observation that not only the union of the spermatia with the trichogyne precedes those characteristic changes and developments, but that these do not take place if the —— for any reason have not made their appearance. We are met by the same arguments and results in the case also of Eurotium, though the facts observed in this case are not so striking at first sight as in Pyronema; and lastly Eidam’s observations on Eremascus show that the union of the protoplasms is as evident as it can be in organs which are extremely similar to those in question in Eurotium, Penicillium, &c. In these cases we may therefore affirm, that, according to our present criteria, the antheridial branches, or the CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES. 235 spermatia which must be supposed to be abjointed portions of such branches, are in function male sexual organs, and that the archicarps are female sexual organs, and that the Fungi which produce them possess the power of sexual propagation. This statement is not admissible in the case of all the other forms furnished with homologous members. Resting on what we know, we may suspect that in Polystigma the trichogyne and spermatia behave in the same way as in Collema, but we have no proof of the necessary material union. In Gymnoascus and the Ery- sipheae, especially Podosphaera, the two organs appear with the same constancy, one might say with the same morphological necessity, as in Pyronema, and the possibility of a material union of the protoplasmic bodies is not excluded by the known facts. The antheridium, it is true, always remains separated from the archi- carp by a membrane which, as far as we can see, is not perforated, but it is closely attached to it, and dissolved or very finely comminuted substance may pass through the membrane, as must be assumed in the case of the fertilisation of Angiosperms. But after all nothing is proved about the matter; the constant contact of the antheridial branch proves nothing; the envelope is constantly in the same position; we cannot get beyond probabilities and possibilities. Beneath the level of probability we arrive at last at species like Melanospora parasitica and Ascobolus, which needs revision however in this respect, with a beautifully developed carpogonium, but with the attachment of the antheridium not constantly or certainly observed. The conclusion on the whole is, that some of the forms in question have sexual organs which can be shown to fulfil their functions, others have organs perfectly homologous with the first, but with the sexual function not certainly _ ascertained or certainly wanting. We have secondly to enquire after the homologies of the Matos cetess in which there is no distinct archicarp, as far as we at present know, when the sporocarp begins to appear. We will consider first the extreme cases, Pleospora and Claviceps. Here the question is, are the parts in these species to be considered as really homo- logous with those of the same name in the other series which has archicarps, or only as very similar to them in form and function ; or, expressed in terms of the phylogeny, do these Ascomycetes belong to a single series of forms descended from the same stock, or to af least two series descended from different stocks only with analogous ultimate construction? We can only advance probable arguments in deciding between these alternatives, but these are against the second of the two and in favour of the unity of the Ascomycetes. First of all the difference alleged is thé only one, while they agree together in all other points of importance to a degree which is else- where found only in allied forms, and not in those which are merely analogously developed. Secondly, no other close affinity can be found for the Ascomycetes which have no archicarps than that with the others; and they must have some relation of the kind, some connection with other forms. Thirdly, the extremes are evidently connected together by intermediate forms. ‘The first of such forms is to be found in Melanospora parasitica with its beautifully developed carpogonium but inconspicuous or absent antheridium ; other like phenomena appear to occur occasionally ' in the series of the Sordarieae, and these therefore claim the attention of observers. Sclerotinia also ? See also Zopf in Sitzgsber. d. Brandenb. bot. Ver. 1877. 236 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. is one of this kind. On the other hand, forms like Xylaria, which have Woronin’s hypha as a transitory formation only, offer transitions connecting them with Polystigma. Amongst the former cases which connect with Melanospora are forms in which at one end of the series distinct archicarps are present functioning as certainly asexual (par- thenogenetic) ascogonia, and along with them distinct elements of an envelope; towards the other end of the series the difference between ascogonium and envelope-formation diminishes till it disappears, and it is only in a more advanced stage of development of the. sporocarp that the formation of ascus and of envelope is undertaken by separate elements, which up to that time were apparently uniform with the rest (Pleospora, Claviceps). Sexuality therefore is not developed, and in the extreme cases there is entire disappearance of primordia of the sporocarp which are homologous with sexual organs. In the other series of cases Woronin’s hypha in the Xylarieae can be under- stood if we compare it with the archicarp of Polystigma or Collema. It occupies the same morphological position, but takes no active part, as far as can be seen, in the formation of the sporocarp, and then disappears apparently without having had any function to perform, while the formation of the asci is undertaken by neighbouring hyphae belonging to the envelope.. Here then there is an archicarp or ascogonium present in form, but it remains functionless in the sense expressed by these names, and the formation of asci falls to the lot of other organs not strictly homologous with it. These facts all lead to the result, that in these extreme cases we are in presence of phenomena, which were spoken of above on page 123 as interruption and restoration of the homology. Such a conception would perhaps be rash, if we had not before us the clear cases above mentioned of the occurrence of this phenomenon in Ferns and Angiosperms ; but, from our acquaintance with it there, we are led naturally to this assumption by arguments which have now been stated. . The species with an aborted Woronin’s hypha and a formation of asci at the same time are parallel to the apogamous Ferns with functionless archegonia and to Angiosperms with an aborted egg-apparatus replaced by adventitious embryos; the rest approach nearer to simply parthenogenetic apogamy, as seen in Chara crinita and the Saprolegnieae, but with the peculiarity that the map6évos itself entirely disappears in the extreme cases. In the above discussions the simple forms which have distinct archicarps, such as Eremascus, Erysiphe, and Eurotium, have been treated throughout as forming an indivisible group of closely related species, and it has been sought to bring the rest into connection with them. More is not at present possible. It ought not by any means to be affirmed that all these forms which serve as points of departure are connected with the same Species outside the Ascomycetes, and that subordinate parallel or diverging series do not proceed from individual forms among them inside the circle of the Ascomycetes. It was shown above that Eremascus comes near the Mucorini, and perhaps special groups of other Ascomycetes connect with -Eremascus. Podosphaera is nearer on one side to the Peronosporeae, on the other to the main body of the Pyrenomycetes, and so on.. But at present we are not in possession of the empirical material necessary for the enquiry into these details, and the main results, as here represented, are not decidedly affected by it. The resemblance also in the development of the sporocarps which we have been considering to that of the Florideae has necessarily always attracted attention, but whether it points to an actual closer affinity must for the present remain undecided; other connection than that to which attention has been called above cannot in my opinion be established. CHAPTER V.—COMPARATIVE REVIEW,.—-ASCOMYCETES. 237 A nearer approximation of the Ascomycetes generally, or of some of them, to the Florideae would not materially affect the conclusions at which we have arrived above with regard to the main questions connected with the homologies. In my first investigations (Beitr. III) into the development of the sporocarps in Erysiphe, Eurotium, Pyronema, and others I called the archicarps and antheridial branches generally sexual organs; and from the great amount of agreement between the sporocarps when fully formed I expressed the conjecture that all the Ascomycetes have homologous and analogous organs for the production of these sporocarps. Others followed me in this view, especially when they became acquainted with individual cases which confirmed it. The investigations which are here communicated have had the result of showing that my generalisation was incorrect, and that the mistake arose not merely from want of consideration of facts not then known, but more especially from not distinguishing sufficiently between morphological and phylogenetic homology and physiological analogy. I trust that I have taken this distinction sufficiently into account in my last special treatise (Beitr. 1V) and in this work. Van Tieghem has been one of the chief opponents of my view, for he takes his ground on forms that have no distinct archicarps and does not allow of ‘sexuality’ in the Ascomycetes. His opinion briefly stated is this, that the differentiation of the ascogenous hyphae and their envelopes takes place at stages in the development of the sporocarp which vary according to the species, and that it occurs at the earliest possible stage in the species which are supposed to have sexual drgans. The supposed female organ is only an ascogenous hypha differentiated at a very early period, the supposed male organs are simply part of the envelope-structures. The facts on which Van Tieghem originally founded his opposition were certainly not happily chosen. But if he is content to rest his case on Pleospora for instance, or-even on the actual condition of things in Sclerotinia with which he has never been acquainted, he must be allowed to be quite in the right as against my original conjectural generalisation literally taken ; and if he objects that the actual sexual function of these organs has not been proved in the case of Eurotium and Podosphaera, he will find that this is allowed in my work of 1870. But Van Tieghem makes no enquiry into the homologies and extends his negation beyond the limits allowed by the facts. If he had duly considered the indisputable fact of the constant presence in Podosphaera of my antheridial branch, that is of an organ distinctly different from the later- formed structures of the envelope and accompanying the proper commencement of the sporocarp, he would have been led to those true subjects of enquiry which have been discussed in the foregoing pages, and which it has been attempted to elu- cidate; and the facts at present known about Pyronema, Eremascus and other forms should have led him to a different answer to his own enquiries. We need not go into his positive views with regard to the function of the organs in question, that, for instance, the antheridial branches serve to support the ascogonium and that the trichogyne in Collema is an organ of respiration, before it has been shown to be to some extent probable that the ascogonia are in danger of falling without this support, and that the particular organ in Collema is obliged to have an apparatus of its own to get air, and cannot respire without it quite as well as the elements of the interior of the thallus near which it is placed. Such fancies must certainly deserve the name of gratuitous hypotheses quite as much as the views which I have here explained. Another opponent of my ideas is Brefeld. He wavers between Van Tieghem’s views on the one hand’, and certain others, which, when stripped of some accessories which do not strictly belong to the question, agree with those of the present work”, I have therefore no reply to make, apart from the corrections of some matters of fact » Bot. Ztg. 1876, p. 56, Abs. 23, and Schimmelpilze, IV, p. 142. ? Bot. Ztg. 1877, p. 371, and Schimmelpilze, 1V. 238 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI, which have been made in previous sections. I shall return in a later page to the matters | which, as I have said, do not belong to this place. DETERMINATION OF IMPERFECTLY KNOWN ASCOMYCETES. Section LXVII. The facts detailed in the foregoing pages were established at first from a comparatively. small number of species, but they nevertheless enable us to pass judgment with tolerable certainty on all the varied phenomena which have been observed in the countless forms of the Ascomycetes, especially the Pyrenomycetes and the Discomycetes ; they are a frame in which the latter may be set. It must at the same time be remembered that very many of these phenomena were known, named, and provisionally disposed of according to the best knowledge of the time before a secure basis was laid for a decision respecting them, and that it was by starting from single phenomena that this basis was gradually reached. Especially should it be remembered (see section XXXII) that at first every distinct form was supposed to represent a distinct sfeczes; the gonidiophores of Sclerotinia Fuckeliana were made a species under the name of Botrytis cinerea, the sclerotia another species as Sclerotium echinatum, while the sporocarps by themselves were made a species of Peziza; in Erysiphe the gonidiophores were supposed to be a species of the genus Oidium, and only the perithecia were assigned to Erysiphe. The researches of Tulasne first led gradually to an understanding of the real condition of things to which’ he gave the name of pleomorphism, and to him we are chiefly indebted for the distinguishing and naming of the possible forms in the development of a species. ‘These researches rested on the broad foundation of the comparative observation of numerous forms, of their cohabitation, of their anatomical - connection, and their succession in time. Pursued in this way they arrived on the whole at the truth, and it is a small diminution of their merits that they should have given rise to some erroneous views on special points, or that they occasionally made a too extensive application of schemes drawn from a number of observations. This latter proceeding led indeed to more important mistakes in the hands of some less careful followers. The task of critical examination could only be satis- -factorily performed after more profound investigation, aided especially by complete experiments in artificial cultivation; and this has resulted in showing that, owing to the great number of the species, the differences in the course of developrhent between the homologous and analogous terminal points which are often very important, and the frequent symbiotic relation social or otherwise between several species, the complications may be much greater than would appear at first sight and than can be expressed by one scheme. Various controversies also have arisen, as appears from the case of Pleospora described above, out of all these labours and efforts which are still far from their final conclusion. Much that belongs to this subject is only of interest in connection with the individual cases and must be referred to in the descriptive literature. We can here call attention only to the chief points of view, but it will be well first of all to enumerate briefly the chief phenomena and members of the development observed in the species above described. 1. From the ascospore is developed a, thallus which only produces asco- genous. sporocarps, or archicarps. which produce these sporocarps together with CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES, 239 antheridial branches and sometimes spermogonia with spermatia, as in Pyronema, species of Ascobolus, and Collema. This may be called the simple course of “development in the Ascomycetes. 2. The dimorphous or pleomorphous course of Gaainnant Similar to the simple one in the terminal points being represented by the ascospores, but Sormations of gonidia are intercalated between them. ‘These formations make their appearance sometimes as a /ranstfory intermediate generation (Polystigma), sometimes as precursors of the ascocarp on the same thallus, and capable under favourable conditions of uniform reproduction through an unlimited number of generations. Excellent examples are Erysiphe, Eurotium, Penicillium, Sclerotinia Fuckeliana. The gonidia are usually acrogenous, seldom intercalary also, in their aa and are produced— (2) On solitary simple sporophores, or sprouting cells. (2) On the exposed upper surface of compound sporophores, as in Claviceps. (c) In peculiar receptacles, pycnidia (pycnogonidia, pycnospores, ‘stylospores ’). Each species can only produce one of these gonidial forms, as is the case with Erysiphe, or under favourable conditions more than one, as Pleospora and Nectria. In all cases that have not been thoroughly examined and are therefore more or less doubtful, an organ or member of the development must be determined and named according to the agreement of its observed characters with those of thoroughly known forms. The correctness of the naming will be more or less certain according to the degree of agreement, and will vary from the extreme of probability to entire uncertainty. The result of this examination of the separate parts and organs is as follows :-— , Section LXVIII. 1. There is nothing to add here to what has been already said of the archicarps and antheridial branches. 2. The sporocarps (apothecia and perithecia) with the asci agree so entirely in the essential points of structure, development, and moment of appearance in the general course of the development, as they are known to us and have been described above, that, as has already been pointed out, they may or must be regarded as generally homologous in the sense and with the modifications above indicated. In by far the largest number of species, as far as our experience goes, they are the most constant members in each species in their structure and especially in the structure of the asci and ascospores. Exceptions to this rule, in which the number or size of the spores is strikingly unequal in different asci, are comparatively rare, and some instances have been mentioned above on page 79. Similar cases are recorded in Pleospora and some other forms. Calosphaeria biformis, Tul. and Cryptospora suffusa, Tul. are said to have two kinds of perithecia, one of which has asci with a large number of small spores, the other asci with from four to eight much larger spores’. How far this is really a case of difference within the same species, and not also of the mixing up of two similar or associated species, should be enquired into, and the investigation is rendered more necessary by the question which has arisen in the case of Pleospora noticed on page 230. 1 Tulasne, Carpol. II. 240 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI. Section LXIX. 3. Spermatia, spermogonia. Organs in every respect ex- ‘tremely like those which are thus named in Collema, Physma, &c. (page 211) are found in almost all the rest of the Lichen-forming Ascomycetes ; the genus Solorina may be* mentioned as an exception among those in which this point has been carefully examined. ‘These organs occur also in many species which do not form Lichens both among the Discomycetes and especially among the Pyrenomycetes. On the ground of these points of resemblance the organs in question are entitled to the names given to the corresponding organs of the Collemeae and Polystigma, and are at least to be regarded as homologous with them. All these organs agree first of all in the formation of sfermatia, small ellipsoid, or more commonly narrowly rod-shaped, bodies, which are often also bent, as in Rhytisma, Diatrype (Fig. 114), and Polystigma. Their absolute size varies much in the different species; those that have the form of narrow rods are according to Tulasne 6 or 7 » in length in species of Diatrype, and as much as 30 p» in Polystigma rubrum, or less than 6 » in some species of Gyrophora (Fig. 100); the ellipsoid spermatia of Peltigera have a length of 12-22 ». Their structure, as far as it can be ascertained, is similar to that of very small and delicate spores with homogeneous FIG. 112. Valsanivea, Tul. Verticalsection through FIG. 113. Zympants conspersa, Fr. ha i i jectii hortly stalked apothecium with two spermo- astroma; in the centre a spermogonium ejecting sper- shortly stat M ‘ spern matia; on each side a perithecium. After Tulasne. gonia at its base, in median longitudinal Slightly magnified. section. Spermatia are escaping from the : spermogonium tothe right. After Tulasne. Slightly magnified. protoplasm, and they are formed in the same way as acrogenously produced spores, being abjointed singly or in rows from short and narrow ends of filaments (sterigmata, basidia); the latter organs vary in the different species and genera, being either elongated and cylindrical, unsegmented or with indistinct septa, and forming spermatia at their apex only (sterigmata in the narrower sense of Nylander), or they are many- membered cell-rows in which the cells are little longer than broad, and form each of * them lateral spermatia close to their upper end (Fig. too B, the arthrosterigmata of Nylander). This latter form has been chiefly, if not exclusively, observed in certain genera of Lichen-fungi. These spermatia are always formed side by side in large numbers, and are imbedded, as in Collema, in a jelly which becomes hard and brittle as it dries, and dissolves and disappears in a super-abundance of water. If they are placed with the jelly in a comparatively large quantity of water, they exhibit a gently tremulous oscillating movement ; but since this movement appears in spermatia which have been killed by boiling or by being treated with absolute alcohol as well as in those which are alive and fresh, it must be considered to be a purely physical phenomenon due to the motion which is caused in the water by the swelling and partial dissolution CHAPTER V.—COMPARATIVE REVIEW.-—ASCOMYCETES, 241 of the jelly, and which must necessarily be communicated to such small and light bodies. ~ , » With these characteristics the spermatia cannot be certainly distinguished from small spores. The distinction however is, that, like those of Collema or Polystigma, they are all, as far as has been hitherto observed, zcapadble of germination. Secondly, these organs all agree in having the spermatiophores collected together into close hymenia in the sfermogonia. ‘These spermogonia are usually, as in Collema and Polystigma, hollow receptacles like perithecia sunk in the tissue of the thallus, with the cavity smooth and pitcher-shaped, or, as is very often the case, repeatedly and very irregularly folded into sinuous depressions and projections, so that where the folds are narrow the receptacle has the appearance in section of being divided into a FIG. 114. Ditatrype qguercina, Fr. @ a spermogonium on a piece of bark, laid open by removing the periderm. The conically pointed upper surface which is folded in coils bears the hymenium of the spermatia. 4 vertical longitudinal section through a spermogonium ; a tendril-like mass of sper- matia is issuing from an opening in the overlying periderm. ¢ fragment of a thin section through the surface of the spermogonium with sickle-shaped spermatia and their sterigmata. After Tulasne. aand é slightly magnified, c magn. 360 times. number of compartments. The cavity is everywhere lined with the hymenium which pro- duces the spermatia, and the spermatia when mature are imbedded in jelly and occupy the centre of the cavity, and when the jelly swells in water they issue crowded together in drops or long strings from the narrow orifice of the spermogonium (Figs. 112, 113). Some Pyrenomycetes which live in the rind of trees form layers agreeing in every respect with the spermatiophores, except that they are not inclosed in receptacles altogether belonging to the Fungus; on the contrary they are disk-shaped or cushion- shaped bodies with the spermatiogenous surface folded into deep sinuous depressions, as in species of Diatrype (Fig. 114), Quaternaria, and Stictosphaeria, Tul., or else smooth as in Calosphaeria princeps, Tul., and in both cases covered only by the peripheral layers of the rind. The spermatia escape through a narrow fissure in the rind, [4] R 242 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. usually formed above a conical projection in the Fungus-body. Since the agreement is otherwise so complete we may certainly consider these bodies as spermogonia which have no outer wall of their own, but are covered over instead by the rind of the tree which they inhabit. But this affords reason for a further concession and allows us to give the name of open spermogonia to such cushion-shaped or club-shaped bodies formed on the surface of the substratum as Tulasne has described in Bulgaria sar- coides and Peziza fusarioides; for the outer surface of these bodies is covered with a hymenium, which, together with its products, behaves in the same way as the hymenium of the closed spermogonia previously mentioned. The third and last point of agreement to -be observed in all the formations of which we are speaking lies in their relation in place and in the time of their develop- ment to the production of the ascocarps. In all cases which have been fully investigated we find the same arrangement as in Collema and Polystigma; the formation of spermogonia and spermatia always precedes that of the sporocarps or coincides with the first appearance of their primordia. At the same time the formation of spermatia may continue beyond the period of the orientation of the sporocarps, and both kinds of organs may be repeated more than once on a long- lived thallus; but this makes no essential difference. The two kinds of organs usually occur close to one another on the same thallus; ‘dioecious distribution, to which attention has been called above in the case of Collema, has been observed a few times in some Lichen-fungi (Spilonema, Bornet, Ephebe pubescens). We do not certainly know the true function of all the bodies which are spoken of in this section as spermogonia and spermatia. What we are able to conjecture on the subject may be gathered from previous sections, and will be considered also below in section LXXIV. Section LXX. We have insisted in the foregoing remarks on the invariably small size of the spermatia, and on their simplicity of structure and incapacity of germination, or, to speak more correctly, the absence of observed capacity of germination; and these conditions make it difficult to determine a number of other cases, which may for the present be placed together under the head of doubtful spermatia. We learn from a series of observations that there are small rod-shaped or spherical cells in the Ascomycetes, which have all the known positive and negative characters of spermatia, but are abscised at other places in the thallus than in or on distinct spermogonia. ; Firstly, such cells are said to occur in the sporocarps themselves, between or near the asci. Gibelli’ states that many Verrucarieae, especially those with simple spores and without paraphyses in the hymenium, have no proper spermogonia, but that the lower portion of the perithecium is covered with asci, the upper with spermatia-forming sterigmata; but other observers* do not corroborate this statement. We learn from Tulasne that slender branched hyphae, from which countless small rod-shaped ‘spermatia’ are abscised, are found between the asci at the places where paraphyses otherwise occur in some but not all the apothecia in ' Sugli org. reprod. del gen. Verrucaria (Mem. soc. ital. di sc. nat. I). * Stahl, Beitr. z, Entw. d. Flechten, I, p. 40. CHAPTER V.—COMPARATIVE REVIEW.—-ASCOMYCETES., 243 his Peziza benesuada (Fig. 115); similar organs occupy the margin of the platter- shaped tube-bearing hymenia of Cenangium Frangulae, Tul. Small round cells incapable of germination, which will be noticed again in a subsequent page, are said by Brefeld! to be sometimes abscised from the ramifications of the b pares! in Peziza Sclerotiorum. The second place where these doubtful ‘ spermatia’ occur is in the pycnidia of certain species, in which spores as well as spermatia are produced; such species, according to Tulasne, are Cenangium Fraxini, Tul., Dermatea carpinea, Fr., D. Coryli, Tul., D. dissepta, Tul., where the spermatia-forming hyphae also occupy chiefly the margin of the hymenium, also in D. amoena, Tul., Peziza arduen- nensis and Aglaospora. Thirdly, small short-lived cells, which do not germinate and may be compared with spermatia, are abscised in many species from filiform branchlets of the mycelium and from the germ-tubes, or even directly | from the germinating spores. Brefeld? found a multitude of such*formations on the mycelium of artificially grown plants of Peziza (Sclerotinia) tuberosa. From short branches, often with tufts of branchlets as in Penicillium, are abjointed successively and serially at the extremities of their ramifications small cells, each containing a small sphere of a highly refringent perhaps fatty substance, and these are cemented together by a jelly and thus collected in heaps on the parent-filaments. Tulasne® found just such formations on the germ-tubes of the same species and on those of Peziza bolaris and P. Durieuana when the spores were sown in water. A similar phenomenon occurs sometimes on old cultures of the mycelium of P. Sclerotiorum, as Brefeld states and I can myself confirm ; but, as far as my experience goes, only in isolated cases which cannot be more precisely defined. _Fic. 115. From the hymenium of Peziza benesuada, Tul. Ascus sur- I observed it also on the young germ-tubes of this species, could te seeearen tee ae but only in a few and these poor and evidently weakly After Tulasne, Highly magnified. plants. The small cells mentioned above which are abscised in the cups of P. Sclerotiorum are similar, according to Brefeld, to those which we are now describing. The same formations appear also not unfrequently on old luxuriant mycelia of P. Fuckeliana grown from ascospores in fruit-juice on a microscopical slide (Fig. 116); and Zopf found quite similar structures, the narrowly flask-shaped sterigmata, singly or in a tuft according to the luxuriance of the individual, on the mycelium of species of Chaetomium, especially on starved specimens, and also in species of Sordaria (S. curvula, S. minuta, S. decipiens), Woronin having seen them ~ before in S. coprophila. Small bodies of the kind here described sprout out directly from the cells of the multicellular compound spores of Tulasne’s* Peziza Cylichnium when sown in water. ? Schimmelpilze, IV, p. 121. ? Schimmelpilze, IV, p. 113. * Ann. d. sc, nat. sér. 3, XX, p. 174, and Carpol. III, t. XXII. * Ann. d. se, nat. sér 3, XX, and Carpologia, III, pp. 200, 202. R 2 244 DIVISION ItI,—COURSE OF DEVELOPMENT OF FUNGI, The small rod-like cells which sprout from the cells of the spores of Nectria inaurata and N. Lamyi? while still inside the ascus, filling it quite full and giving rise to strange misunderstandings, may also be mentioned in this place, thoughit is not very probable that they are of the same significance. The point of agreement between all these forms lies in their outward resemblance and in the absence of any certain knowledge as to their morphological and physiological value. Section LXXI. 4. Gonidia. The course of development in the few forms mentioned above on page 238, 1, is shown with certainty by our observations up to the present time to be that which is there termed simple ; and almost all Lichen-fungi also are without gonidia unless we count among them the soredia, which will be described in section CXVII, as there is certainly good reason for doing ; other gonidial formations are described in a few species only, as ex- ceptional cases therefore, and in these are not beyond doubt. ° The course of development in the larger part of the Ascomycetes with which we are acquainted, and especially in the Pyrenomycetes, is pleomorphous with copious pro- duction of gonidia of more than one form, All the gonidia are unicellular or pluricellular compound spores formed by acrogenous or intercalary abjunction, as in the ex- amples which have just been described. Anatomical investigation and observation of different portions of the development show that they usually appear as precursors of the ascocarps, whether their development comes to an FIG. 136, Pesiza Fuckeliana. Froma €nd when the formation or at least the completion of these. sesoec Sica Saneseee AUC Sian begins, or they make their first appearance before the stcrigmats forming “spermatia’ a the latter but continue to develope simultaneously with them. Gpinchin shown ticks a ts tithe Claviceps, which has already been described, is an excellent Spin gate ce tele ees example of the first case, for gonidia and perithecia follow Seeaae ten ane, hen aie coe one another in that genus in successive periods of vege- aaancs merch cutlined) of spermatia tation. The development of species of Stigmatea accord- ae tence ns mbeddedin jelly. Magn. in to Tulasne’, and probably of some other small Pyre- nomycetes that live in leaves, follows a similar course, but without forming sclerotia ; and this is the case also with Epichloe, which was described in a former page, and with Tulasne’s Xylarieae (Xylaria, Poronia, Ustulina, Hypoxylon) and some species of Nectria, especially N. cinnabarina (=Tubercularia vulgaris, P.), which all behave in a similar manner to Epichloe. The compound sporophores of these forms are at first covered by a hyménium which produces gonidia, but this ceases to grow and is cast off as soon as the development of the perithecia formed within its plane of insertion begins to advance. A second case is exemplified in the Erysipheae mentioned above, in Fumago salicina*, Cucurbitaria macrospora (Fig. 117), Pleospora polytrichum, P. Clavariarum ¢, 1 See Janowitsch in Bot. Ztg. 1865, p. 149. 2 Carpol. II. * Tulasne, Carpol. IT. 4 Tulasne, Carpol. II. CHAPTER V.—COMPARATIVE REVIEW,—-ASCOMYCETES, 245 and some others. Ripe and ripening perithecia may-in these plants stand side by side on the same mycelium or stroma with developing gonidiophores. It is scarcely necessary to remark that the succession of events does not always proceed in these examples with perfect regularity; and the instance of Peziza ’ Fuckeliana described above on page 224 shows that considerable deviations from it may and do occur. As regards the point of origin of the gonidiophores and their arrangement and structure, it would seem that they occur in particular species in the ascocarps them- selves, like the doubtful spermatia noticed on page 242. According to Berkeley’ single paraphyses are found between the asci in Sphaeria oblitescens B. et Br., in which one or two of the cells are enlarged into somewhat elongated septate ‘spores;’ the terminal cells of such paraphyses in Dothidea Zollingeri, Berk.’ are like simple ellipsoid spores. Berkeley* makes a similar statement in the case of a species of Tympanis and for Lecidea Sabuletorum* or an allied form; but these points require re-examination, as Tulasne has intimated®, because we are still ignorant of the qualities of these spore-like bodies. Putting aside these few doubtful and possibly exceptional cases, all gonidial formations conform to the examples described above which have been thoroughly examined. The following special forms may be enumerated :— (a) Free filiform gonidiophores; often very characteristic in their conformation, as in Penicillium, Eurotium, Erysiphe, &c., and in such cases formerly assigned to established form-genera. ‘Thus species of Hypomyces were assigned to the form- genera Verticillium, Sepodonium, and Mycogone of the old descriptions, and Fusisporium Solani®; species of Nectria to Fusisporium and Spicaria of the old descriptions, and many other cases might be cited. To these may be added some other forms, in which the distinction between gonidia and gonidiophores on the one hand and portions of the mycelium on the other is less sharply defined, and may even be arbitrary in each individual instance up to the extreme cases in which each cell of a hypha or a hyphal strand first performs the part of a mycelium and then assumes the characters of a spore. The latter is in extreme cases naturally termed the formation of resting mycelium and has been elaborately studied by Bauke and Zopf, éspecially in saprophytic Pyrenomycetes, though older observers often men- tioned it incidentally. It occurs in old and specially in starved mycelia for example of Pleospora, Fumago, and Cucurbitaria, in which the cells of the mycelium acquire thick and usually brown walls, store up reserve food material, and pass into a dormant state, and subsequently under suitable conditions germinate as spores. Changes of form, especially swelling of the individual cells into a spherical shape, may or may not accompany the changes which characterise the state of rest, and hence the resting states differ in very various degrees from the vegetative mycelial forms. 1 Ann. Mag. Nat. hist. ser. 3, III, p. 373, t. XI, 32. * Hooker’s Journ. III (1844), p. 336. 5 Introd. Crypt. Bot. p. 244. * See Ann. Mag. Nat. Hist. ser. 2, IX, and Crypt. Bot. p. 391. 5 Mém. s. les Lichens, p. 110. ® Reinke u. Berthold, Die Zersetzung d. Kartoffeln durch Pilze, 1879. 246 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. (4) Dense hymenia giving off gonidia by abscision on the free outer surface of compound sporophores. Examples of this kind are Claviceps (page 227), Epichloe, the Nectrieae before mentioned, Xylarieae (Fig. 103 A), Cucurbitaria macrospora (Fig. 117), and many others. The form of the separate gonidiophores which together constitute the hymenium, the special mode of abjunction of the gonidia, and the structure and form of the gonidia themselves, all vary extremely according to the species. And again it depends on the species whether the formation of gonidia is entirely, or almost entirely, confined to these hymenia or to the stromata which bear them, as is the case in Nectria cinnabarina and the other genera last named, or whether gonidia-forming hyphae of like structure occur either united into hymenia or appearing singly on a filamentous mycelium as in the Hyphomycetes, as happens in Nectria Solani and Hypomyces Solani’. Whether we have always to do with gonidia in the cases which have been given as examples, especially in the Xylarieae, or sometimes also with non-germinating spermatia, is often uncertain and must be determined in each separate case. (c) Pycnidia: receptacles (conceptacles) of more or less similar character to those described in Pleospora, and producing gonidia which are known as pycnospores or pycnogonidia or more commonly as stylospores. They are wanting in many or most species of Ascomycetes, in all forms, for instance, mentioned under 8 and in most of those mentioned under a, and in almost all Lichen-fungi. They were said indeed to have been found by Lindsay in Bryopogon jubatus, Kbr., Imbricaria saxatilis and I. sinuosa, Kbr. ; by Gibelli in ‘ Verrucaria carpinea, Pers.,’ Sagedia carpinea, Mass., S. Zizyphi, Mass., S. callopisma, Mass., S. Thuretii, FIG. 117. Cucurbitaria macrospora, Ces. and de Not. a stroma. . os ° in longitudinal section; developed perithecium, c layer of gonidia. Kbr., Pyrenula minuta, Nag., P. olivacea, p tptoniy wetiem Aak oe en ete Pers., Verrucaria Gibelliana, Garov.; by Fiiisting in Opegrapha varia, Acrocordia gemmata, Mass., A. tersa, Sagedia netrospora, Hepp., and S. aenea. Lindsay's account also of two kinds of spermogonia in Roccella Montagnei, Bel. and Opegrapha vulgata, Ach. may be mentioned here since some of the receptacles which he termed ‘ spermogonia may be pycnidia. But in all these cases we know so little concerning the development of the organs in question that it is still uncertain whether they belong to the species named above or to parasites living in their thallus. The pycnidia, like the perithecia, are according to the species either formed singly from the filamentous mycelium, or are placed in or on compound pycnidio- phores (stromata), as in Cucurbitaria Laburni, Dothidea Melanops, &c.? Their development proceeds, in several cases that have been observed, in the manner ‘ Reinke u. Berthold, Die Zersetzung d. Kartoffeln durch Pilze, 1879. * Tulasne, Carpol. IT, CHAPTER V.—COMPARATIVE REVIEW.—--ASCOMYCETES. 247 described above on page 229, in the case of Pleospora; an intercalary portion of a mycelial filament grows by successive divisions which arise without fixed order in every direction, and the cells thus formed are subsequently differentiated, while branches from adjoining hyphae usually grow up round the new body and thus help to form its wall (see Fig. 118). This is the mode of formation according to Gibelli and Griffini, Eidam and Bauke not only in Pleospora herbarum, but also in Cucurbitaria elongata, Leptosphaeria doliolum and two other species not precisely determined, and according WZ =—s A Bay mi im, eps ean fey SEY ee Kt 7 a7 oe, eee Ti a b FIG. 118. Pleospora Alternariae, Gibelli. (Determination not certain FIG. 119. Cicinnobolus Cesatiz (De Bary, Beitr. III), para- from the absence of perithecia.) Young stage of development of pycnidia. sitic on Erysifhe. Aripe pycnidium (seen from without) @ commencement of the swelling and rapid transverse division of the open above on the left and discharging its spores s, having de- intercalary portion of a hypha, which is developing into a pycnidium and veloped in a gonidiophore of the Erysiphewhich is attached has branches from itself and from an adjacent hypha attached to it. tothe mycelial filament x x and bears four dead gonidia ¢ on 4 older stage of the development. The mature structure of these pycnidia itssummit. 2asmall and nearly ripe pycnidium, formedona closely resenibles that represented in Fig. 119, only the wall is formed of branch of a mycelial hypha m of the Erysiphe, in which several layers. Magn. 600 times, the slender mycelial hyphae of the Cicinnodolus may be seen. The figure shows the upper surface and the optical longitudinal section of the transparent peridium; the section shows the young spores growing inwards from the one- layered wall. C tranverse section through the wall of a ripe pycnidium with three primordial spores sprouting inwards. D two ripe spores just discharged from the pycnidium and a germinating spore. 4 magn. 380, B, C 600, D 300 times. to Zopfin some pycnidia of Fumago ; Brefeld’s ‘Pycnis sclerotivora’ must also be added to the number. Other pycnidia are not meristogenetic but symphyogenetic formations, that is, they are produced by union and interweaving of hyphal branches; such are those known under the name of Cicinnobolus, some in the genus Fumago, and the Diplodia-form examined by Bauke. The formation of the pycnidia in Pleospora polytricha, according to Bauke, is of an intermediate kind, the inner portion being meristogenetic and the numerous outer wall-layers symphyogenetic. The structure of pycnidia formed in these different ways may be quite alike in the matured state, as is seen by comparing Cicinnobolus (Fig. 119) and Pleospora. 248 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. The shape of the pycnidia isin general the same as that of perithecia or spermo- gonia, and the internal cavity, like that of the spermogonia, is according to the species either simple or divided by projections from the wall into usually irregular narrow compartments communicating towards the orifice. ‘The pycnospores of the different species exhibit the usual variety of modifications in the structure of spores. Two extreme forms may if necessary be distinguished : smad/-spored pycnidia (corresponding to the old form-genus Phoma) with very small, colourless, somewhat elongated spores, which are imbedded in mucilage and are discharged in masses from the orifice of the pycnidium, as in Pleospora and Cucurbitaria elongata, and J/arge-spored pycnidia with comparatively large either simple or compound spores, the walls of which are often thick and of a brown colour. Section LXXII. In the species of which we are now speaking, as well as in those previously described and which have been thoroughly examined, the different forms of gonidia and gonidiophores occur according to the species in the greatest possible variety of combinations with the perithecia and sometimes with one another. Examples of this, such as may be considered to be well ascertained, are to be found in the works here quoted, and especially in Tulasne’s Carpologia. Some of the accounts contained in this book, and still more those in the more recent de- scriptive writings, must be accepted with caution. We may here call attention more distinctly to the fact, which may be gathered indeed from some of the previous remarks, that each species has the faculty of forming asci and gonidia within broader or narrower limits as the result of its inherent inherited qualities; external causes, especially the quantity and quality of the food at its disposition, then determine in a variety of ways the phenomena which are actually observed. A few examples will now be given in illustration especially of the latter point, which will be further discussed in section LXXIII. The genera Ustulina, Poronia, and Hypoxylon among the Xylarieae may be con- sidered, as far as we at present know, to be plants of one form, since, like Epichloe _ (and Claviceps), they produce gonidia of owe definite form on the young stroma, and then perithecia. Cucurbitaria Laburni! forms in the dead rind of Cytisus Laburnum large. flat roundish cushion-like stromata which reach a breadth of some millimetres and finally issue from the ruptured periderm covered with numerous black round spore-receptacles. Some of these are perithecia, some gonidial receptacles, pycnidia, with a single cavity and a narrow canal at the orifice ; a stroma according to Tulasne may bear only peri- thecia or only pycnidia, but usually has both and more than one kind of pycnidium. In the latter case the receptacles make their appearance on the stroma, which increases in size while they are forming, in adout the following order in time and centrifugal succession :— 1. In the middle of the stroma one or a few comparatively large colourless pycnidia, producing colourless thin-walled unsegmented cylindrico-elliptical spores 5-10 p in length, on short sterigmata. z. Numerous pycnidia with thick black walls in which are abscised from short sterigmata (a) Colourless spores of very unequal size, ? Tulasne, Carpol. II, p. 215, t. XX VII. CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES, 249 (4) Spores with dark brown walls, nonseptate or with one transverse wall, closely resembling the spores of No. 1 in form and size, (c) Brown spores like the last but pluricellular compound, 20-30 pin length and 7-10 » in breadth. Each of these spore-forms generally occurs separately in a special receptacle, so that four kinds of pycnidia may be distinguished; but combinations are also found especially of (a) and (c) in the same receptacle. 3. The perithecia. . The formation of germ-tubes has been observed in all the forms of spores produced in the pycnidia. No other gonidial forms are found in Cucurbitaria Laburni. Species of Hypomyces are characteristic examples of the regular formation of two kinds of gonidia; these plants, like Hyphomycetes, live on the larger Fungi, especially the Hymenomycetes, Hypomyces rosellus for instance, H. chrysospermus, and other species’, or on parts of dead plants, as H. Solani on rotten potatos”. Besides the perithecia which are comparatively rare, and are always later in their appearance, the mycelium produces (1) Microgonidia, comparatively thin-walled and colourless, but tolerably large, ellip- soid, cylindrical, or fusiform unicellular or compoundly pluricellular spores, which are abjointed successively and form small heads at the extremities of the ramifications of verticillately or irregularly branched gonidiophores, and were assigned to the old form- genera Verticillium, Dactylium, Fusisporium, and others. (2) Megalogonidia or macrogonidia, sometimes also called chlamydospores, acroge- nously formed and solitary or more rarely appearing a few together one behind another on branches of the hyphae which produce the microgonidia ; their formation generally begins later than that of the microgonidia, from which they are distinguished by their thick membranes, which are often rough with warts and usually coloured, and in most species by their greater size; they are unicellular or compound pluricellular according to the species. The thickness of their membranes shows that they are adapted to a persistent state of rest. Reinke and Berthold have shown that in Hypomyces Solani mycelia are formed from the germ-tubes of both kinds of gonidia as well as of the ascospores, which can again produce both kinds of gonidiophores, and Tulasne’s less complete account agrees with theirs. More complete knowledge of the general course of development has not yet been obtained. ; Zopf’s Fumago* may be adduced here in conclusion as an example of a cycle of forms still more copious and varied than that of Pleospora or Nectria ditissima which have already been described. Though Zopf found no ascocarps in his Fungus, yet I place it here with the Ascomycetes, because according to Tulasne‘ the very similar species Fumago salicina has ascocarps, and because we are specially considering at the present moment the Ascomycetes which are not yet quite perfectly known. The species of Fumago are the soot-dew which is found in the form of black fuliginous coatings covering parts of living plants. Zopf studied his plants chiefly in pure cultures on microscopic slides in nutrient saccharine solutions of various degrees of concentration, and ascertained the agreement of the cultivated forms with those which occur in nature. 1. The mycelium of the Fungus is composed of hyphae with short segments, which, like the cells of the gonidiophores, acquire usually at an early period a brown coloration of the walls accompanied by a gelatinisation of an outer colourless layer, while the ? See Tulasne, Carpol. IIT. ? Reinke u. Berthold, as cited on page 245. * Die Conidienfriichte von Fumago (N. Act. Leopold. XL). * Carpol. II. 250 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI. cell-contents develope much fatty matter. The gonidia are formed acrogenously on distinct gonidiophores, or in gonidial receptacles, and may be termed acrogonidia. They are when first matured small thin-walled colourless ellipsoidal cells with a gelatinous outer covering and a small drop of fatty matter in the focus; in size they are 4-5 » in length and 2 » in breadth, and are formed in a variety of ways. (a) In specimens grown in a poor solution (containing at most five per cent. of nutrient matter) and kept as dry as possible the poorly developed mycelium produces small slender filiform erect gonidiophores composed of a few cells, which form their acrogonidia successively like heads at their apex, or in whorls beneath the upper end of their subterminal cells (Zopf’s formation of microgonidia). (4) Stronger mycelia are developed with a more generous supply of food, and these produce erect tufts of many-celled hyphal branches on which acrogonidia are formed. From 2-12 of these branches grow close together, at first closely parallel to one another, but afterwards diverging at an acute angle, and may be nearly a millimetre in height ; the branches in a tuft are of a nearly uniform height. The lower cells of each hypha are elongated and cylindrical, the upper short, scarcely longer than broad, and from them proceed other branches with short cells usually placed on one side only of . the cell from which they spring, and rising in the same direction and to nearly the same height as the primary branch, thus resembling to some extent the tuft of branchlets at the extremity of the gonidiophore of Penicillium. From the short cells of all these tufts of branchlets acrogonidia are abscised, terminal ones at their apex, the rest near their upper bounding wall, and all usually on one side and in the same direction. (c) The tufts of gonidiophores formed on the mycelium in the way described under division (4) may be firmly united into a bundle along their whole length, while their other characters remain the same. This bundle is at first nearly cylindrical, but its apex spreads out into the shape of a funnel as the terminal ramifications are being formed which will produce gonidia, and their extremities spread out from one another in a penicillate manner; the abscision takes piace only inside the funnel-shaped enlargement, the outer side remains sterile, and the pointed barren extremities of its hyphae extend with a slight divergence a short distance above the tuft from which the gonidia are abscised. (d) The sterile extremities of these hyphae may unite laterally and firmly into a narrowly conical tube open at the top, and grow out far beyond the region which supplies the gonidia; in other words they form a symphyogenetic gonidial receptacle, a more or less elongated flask-shaped pycnidium. The ventral portion of the flask is the region from which the gonidia are abscised, and Zopf found that the process was always carried on from the cells of the wall which continues to be of one layer, and not from other hyphal branches which project into the interior of the tube. (e) Lastly, pycnidia of essentially the same definitive structure as those in (d) only of roundish less elongated form, with a wall that is usually two-layered, may also be formed meristogenetically. Intermediate forms are found, as might have been expected, between the formations described above from (c) to (e) inclusively. 2. The acrogonidia when sown in a dilute (five per cent.) nutrient solution sprout and form successive roundish ellipsoid sprout-cells like those of Saccharomyces Cerevisiae ' if the supply of atmospheric air is restricted ; with free admission of air the sprouts are frequently elongated cylindrical shoots (the ‘ Chalara-’ and Mycoderma- form). 3. All the parts and forms of the Fungus which have now been described may pass, if the supply of food diminishes slowly, into resting states under a great variety of particular forms, while the cells swell, acquire a brown colour and store up fatty ? But they incite no alcoholic fermentation. CHAPTER V.—-COMPARATIVE REVIEW.—ASCOMYCETES. 251 substances; thus we get resting gonidia, resting gemmae, and resting mycelia, the latter often appearing as torulose filaments or crust-like masses. All the gonédial and resting forms are capable of germination under favourable conditions, and a@// the forms included in divisions 1, 2, and 3 may be changed into one another if the conditions of growth are suitably varied. ; We must not enter here into the question whether Fumago has other organs of propagation besides the perithecia which are said to occur and those which may possibly occur, though it is one which may very well be asked after Tulasne’s account of F. salicina’. Section LXXIII. It is almost to be expected in the case of pleomorphous species of Ascomycetes, that only separate members of their form-cycle should often be found on a substratum at any given time, whether ascocarps or gonidio- - phores or gonidial receptacles. The frequency of this occurrence in a particular species will depend on the ease with which it spreads as a rule over different kinds of substrata under a great variety of external conditions, and on the other hand, also on the strictness with which it is tied to special conditions of vegetation, in order to produce the particular member which closes the cycle. Examples are seen in the species of Fumago, Pleospora, and Penicillium, and in Sclerotinia Fuckeliana which have been described above; the mycelia of these Fungi bearing simple gonidiophores are of universal occurrence in the form of Moulds, and they are propagated in the same form, while the sporocarps are much more rarely found; the conditions under which they occur in the first two genera are not yet precisely ascertained’; in Penicillium they are produced on plants artificially grown on bread and spontaneously on the skins of grapes that have been pressed for wine, and in Sclerotinia Fuckeliana only on sclerotia which have developed and arrived at a certain degree of maturity on particular foliage-leaves (Vitis, Castanea, Quercus); a large number even of the sclerotia of this species produce only new gonidia, as is especially the case with those which are so common on dead cabbage-stalks, the Sclerotium durum of old writers. The majority of known species which form gonidia behave in a similar manner; the converse proceeding, a comparatively copious formation of sporocarps with scanty production of gonidia, is comparatively rare, though it does sometimes occur, as in Melanospora parasitica. Many or indeed most of the gonidial forms of species that are now better known were for these reasons described as form-species, before their genetic relations had been ascertained, and were distributed into corresponding groups, the pycnidia and spermogonia being arranged in the Sphaeropsideae, Cytisporeae, and Phyllosticteae *, the simple hyphal gonidiophores and open hymenial layers in the Hyphomycetes, Haplomycetes, and Gymnomycetes of Fries. Proof of this statement is to be found in the special descriptive literature, to which reference here is unnecessary, since the historical facts are of the same kind as those to which attention was called above in the case of the Mucorini, Peronosporeae, and other forms. ss Another fact which was noticed in the description of those groups is also repeated in the Ascomycetes, namely, that there are forms which strongly resemble the members of the development of thoroughly well-known species, some even ? Tulasne, Carpol. II. ? Ibid. * Fries, Summa Veget. Scand. II. 252 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI. exhibiting the same comparatively minute specific distinctions, but in which the formation of an ascocarp such as belongs to the particular development has never been observed, while at the same time there is no reason for considering that they belong to any group outside the Ascomycetes. We are compelled by this condition of our knowledge to regard these isolated forms as homologous with those which are like them and the position of which is known in the course of development of other species, and to call them accordingly spermogonia, gonidiophores, pycnidia, or the like; it is true that this practice is founded only on probabilities, but it has already found its justification in many cases in the strict proofs which have been subsequently obtained. Most of the Haplomycetes, Gymnomycetes, Sphaeropsideae, &c. of the old systems, one might indeed say all of them that do not belong to the groups described in the previous sections, fall in this way and in accordance with the present state of our knowledge into the class of Ascomycetes, some connecting immediately with well-known ascomycetous species, others through the forms first mentioned; the grouping of the very large number of species and particular forms is necessarily attended with practical difficulties of a different kind from those which are met with in dealing with the few dozen Mucorini or Peronosporeae. While referring the reader to the descriptive literature of this subject, it may be well to mention a few names in illustration of the above remarks ; most species for instance of the old form-genera Naemaspora, Cytispora, Libertella, Septoria, Lepto- thyrium, Phyllosticta, Cheilaria, Gloeosporium, Spilosphaeria, Ascochyta, Phoma, Diplodia, Myxocyclus, Hendersonia, Sporocadus, Sphaeropsis, Cicinnobolus, Ehr. and some others must be classed with the pycnidia and partly also with the spermogonia ; species of the form-genera Cylindrosporium, Oidium, Dematium, Conoplea, Periconia, Cladosporium, Helminthosporium, Macrosporium, Dendryphium, Mystrosporium, Brachycladium, Sepedonium, Mycogone, Aspergillus, Verticillium, Polyactis, Botrytis, Fusisporium, Alternaria, Torula, Isaria, Stilbum, Atractium, Graphium, Melanconium, Stilbospora, Steganosporium, Coryneum, Exosporium, Vermicularia, Tubercularia, Sphacelia, and many others, whose affinity to undoubtedly typical Ascomycetes is either certain or very probable, go with the filamentous gonidiophores and open gonidia- bearing hymenia. To these may be united with the needful reservation a large number of forms, in which the mycelium and the formation of spores, which must be considered homologous with the gonidia, are all that is at present known. Some of these forms do actually belong to the above form-genera, for the determination of these genera was made to rest on certain particulars of conformation which in some cases appear to our present knowledge to have been very superficially examined, and which, as we have since learnt, may occur in very various genetic connections. For instance Oidium leuco- conium, Desm, and O. erysyphoides, Fr. are names for the gonidiophores of Erysipheae. Oidium fructigenum, Kze. and O. lactis, Fres. are somewhat similar forms which do not belong to the Erysipheae and whose genetic affinities are quite unknown ; Botrytis cinerea is the name of Sclerotinia Fuckeliana when it produces gonidia; B. Bassii denotes an isolated gonidial form by no means closely related to the last-named Botrytis. Other forms of this series are so widely different from those named above that the old describers gave them distinct generic names; thus they called their Hyphomytetous forms Arthrobotrys, Gonatobotrys, Haplotrichum, Cephalothecium, Stysanus, &c. &c. These forms are for the present arranged with the Ascomycetes, because from what we know of them they appear to have more connection with that division than with other Fungi; but they are only known to us under one form, which may be considered to be that jn which they produce gonidia. CHAPTER V,—COMPARATIVE REVIEW.—ASCOMYCETES. 253 It may be affirmed of the majority of the species which have just been con- sidered, that they are imperfectly known, because no attempt has been. made to ascertain the entire course of their development. But some among them have not only been observed in the mature state or occasionally grown from the spores, but have been repeatedly submitted to long and careful observation and cultivation; and yet they are only known to produce the same supposed gonidial forms, and there is no sign of ascocarps or of any other member of the development, which the analogy of very similar forms in well-known species would have led us to expect from them. The large species, Aspergillus clavatus’ for instance, has never been known to produce anything but gonidiophores; the sporocarps like those of Eurotium and Penicillium, which were to be expected from the structure of the gonidiophores and of the mycelium, never made their appearance either in Wilhelm’s many experi- ments in the artificial cultivation of the plant, which were made for the purpose of determining this point and were conducted under a variety of conditions, nor in many others which I have myself often repeated in the course of years. Botrytis Bassii*® is a very common insect-destroying Fungus, which in the character of its vegetation is very like Cordyceps militaris, but resembles another Pyrenomycete, Hypocrea rufa*, in the way in which it forms its exposed gonidia; hundreds of cultivated specimens of the plant have produced only the same organs bearing gonidia, never a sign of perithecia ; my conjecture *, which has become an assertion in Brefeld °, with regard to the latter has proved therefore to be incorrect. The same must be said now of another insect-killing form which agrees very closely with Cordyceps militaris in the mode also of forming its gonidia, and which I have described under the name of Isaria strigosa®. Another instance which may be noticed here is the universally distributed and repeatedly cultivated Oidium lactis ; this plant never produces anything but the mycelium with cylindrical serially abjointed gonidia’, The common Cladosporium herbarum, Lk. also should not. be forgotten in this connection. Further instances of this kind have been discovered in the course of the investigations which have been made into the pycnidia. I refer to Zopf’s account of Fumago of which a résumé has just been given. Brefeld® cultivated a pycnidia-bearing form, a not uncommon parasite on the sclerotia of Sclerotinia, under very varied conditions through more than a hundred successive generations, without ever obtaining anything but the pycnidium-form. Similar results are recorded for other species in Bauke’s work on pycnidia; Ehrenberg’s Cicinnobolus, a parasite on Erysipheae*®, may also be quoted here, and it may be added that the pycnidial forms mentioned here are so like others which undoubtedly belong to typical Ascomycetes, that they may be readily mistaken for them. In view of these facts of experience the question again arises which was discussed above in connection with the Mucorini and Peronosporeae whether we have before us species which are only imperfectly known to us, and which under 1 Desmaziéres in Ann. d.sc. nat. sér. 2 (1834), II, tab. II. Fig. 4.—K. Wilhelm, Dissert. p. 62. 2 See Bot. Ztg. 1867. ® Bot. Ztg. 1869, p. 590. * See Tulasne, Carpol. IIT. 7 See above at p. 67. * Bot. Ztg. 1869, p. 590. § Schimmelpilze, IV, 122. 5 Schimmelpilze, IV, p. 136. ® Beitr. III, and above, Fig. 119. 254 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. certain conditions do really fill up the gaps in our knowledge, that is, are able to produce the typical ascocarp of an Ascomycete; or whether there are species which in their known characters do come near to typical Ascomycetous genera and may even be included in them, but do not at present actually produce the ascocarp of an Ascomycete. In the latter case a further question arises, whether and how far the problematic defect comes from the loss of the capacity or from its having never been possessed. The attempt to examine and answer these questions leads us necessarily into the domain of conjecture, and forces upon us the reservations here proposed. Every new unexpected fact may change the grounds of the decision. If we begin with the second question from the stand-point of our present knowledge, we must conclude that the plant has /ost the capacity, as long as the views on the unity and affinity of all the Ascomycetes and on their homologies and connection with the Peronosporeae, which were developed above in section LXVI, are not shown to be incorrect. This is the necessary result of what has been already stated and does not require to be again explained. Whether the loss has in every case directly befallen the species 4 under observation, or another ” from which 4 is descended, must remain an open question and is not an essential element in the matter. The assumption of such a loss would also be in harmony with other known facts in the Fungi which imply retrogression in the development of a species with excision of certain members (see below in section LXXXII). Moreover there are distinctly observed facts within the group in question, which enable us to form a clear idea of the way in which this loss may be occasioned; but these very facts themselves compel us to be cautious and to leave it to time to give a decided answer to the second as well as to the first of our questions. These facts are, first, that some species of Ascomycetes, as has been already pointed out more than once, form their ascocarps only under fixed and narrowly limited conditions, while they reproduce themselves by forming gonidia under very varied conditions. Of this fact Penicillium, Peziza Fuckeliana, Zopf’s Fumago, and the species of Hypomyces described above, are examples. Secondly, there are pleomorphic species which also show a marked tendency to the reproduction of like forms when the conditions remain unchanged, that is, each spore-form chiefly produces its own form again, more rarely a form of another kind, Peziza Fuckeliana is an excellent example of this. If the gonidia of this Fungus, the spores of ‘ Botrytis cinerea,’ are sown in a good nutrient solution, grape-juice for instance, the product is always a filamentous mycelium with copious formation of gonidia. If the ascospores are sown in the same solution under exactly the same conditions, a mycelium is developed with sclerotia, but gonidiophores never or scarcely ever appear ; wherever they have appeared they have appeared singly, and cases of the kind are highly exceptional and not free from suspicion on the score of the purity of the sowing. If similar sowings are made on suitable dead leaves of Vitis or Castanea which have been boiled to free them as far as possible from foreign spores, sclerotia are generally developed ; if ascospores are sown, sclerotia only are formed without filamentous gonidiophores ; if gonidia are sown, the sclerotia are accompanied by an abundance of gonidia which spring from the filamentous mycelium. In cultures of the latter category single gonidiophores may certainly be produced from a sowing of ascospores, just as they may be developed, as is well known, from the sclerotia (see on page 224). The general result which is the CHAPTER V.—-COMPARATIVE REVIEW.-—ASCOMYCETES. 255 important point here, the tendency to the reproduction of like forms, is not the less manifest. Similar relationships appear to exist in Pleospora herbarum (or Gibelli’s P. Alternariae), but I cannot speak decidedly respecting them. By corresponding relationships I should now be inclined to explain the facts, observed by myself in connection with the reproduction of like forms in the gonidial form of Cor- dyceps known as Isaria farinosa’, which led to a controversy respecting its con- nection with the cycle of development of Cordyceps militaris, for which Tulasne contended. Moreover it must easily happen, that in species which show the tendency in question, this tendency and the external conditions work together in the same direction, and the possible consequences of this co-operation can be readily con- ceived. The long-continued effect of the combined conditions might ultimately result in the permanent separation of the originally connected forms, each preserving its existence as a species. This means that each loses the other out of its cycle of development, whether the other continues a separate existence or for any reason dis- appears. It is quite conceivable that species of Ascomycetes producing gonidia only like those described above might originate in this way. . On the other hand, we have to consider that the two sets of causes determining the production of forms in these Fungi, the external and the internal, also work in opposite directions, and that the external causes may eventually overcome the internal tendency and lead to the reproduction of the other form from the one first produced. We may also imagine a przorz that there are cases in which special conditions must combine to produce this result, cases in which the few observations that we possess do not acquaint us with the real conditions, though they are perhaps very simple. Ten experiménts may be made with a similar result under different conditions, and the eleventh may all at once give a totally different result. Experiences of this kind are quite common in this portion of the field of research. These facts admonish us to be cautious, and require that the suggestions in the text should once more be expressly declared to be only very guarded conjectures. Section LXXIV. No less caution is advisable in determining some of the organs which have been described above as doubtful, and we must say a word more about them in this place. The attempt has more than once been made to remove the doubt which exists as to their real nature by declaring them to ‘be rudimentary (rudimentar). It will be well therefore to remember that organs or members are said to be rudimentary which do not reach the height of development attained by their homologues but are stunted in their growth, that is, remain stationary at a stage in their development in which they are in every respect immature; such are the rudimentary stamens of Salvia and of some diclinous flowers. It is true that the term rudimentary has been used in another sense, when an organ is highly developed, but is not properly ‘adapted to the function usually discharged by its homologues, being applied to some other purpose through a necessity resulting from its high organisation, as, for instance, the median staminode of Cypripedium. In some cases this mode of expression may be obvious and therefore admissible, especially as there Bot. Ztg. 1867, 186g. 256 DIVISION II,—-COURSE OF DEVELOPMENT OF FUNGI. are many gradations in the scale of arrestment and of perfection. Still it is more correct in such cases to speak not of arrest of development, but of different adapsation, or the mefamorphosis of members, as we call foliage leaves, tendrils, and anthers in their various adaptations metamorphosed leaves or phyllomes, but do not call foliage- leaves rudimentary anthers, or anthers rudimentary foliage-leaves. At present we will keep to the correct and customary usage and apply the term rudimentary to those parts only which are arrested in respect to their development as members or structures, and also as regards their capacity in every respect for discharging their proper functions. There is still another phenomenon which is allied in many points to unusual metamorphosis and rudimentary development of members and yet is distinct from it, namely, the occurrence of organs which are well developed and capable of performing their function, but which, as far as can be ascertained, are actually functionless. The phenomenon is of course rare ; but the antheridia and archegonia of the apogamous Ferns? afford an example of its actual appearance among the organs of reproduction, which, from the facts recorded elsewhere, may be considered as beyond doubt. The occurrence therefore of this phenomenon must not be forgotten when we are engaged in decidiag about doubtful formations. The doubtful formations which we have to consider here are first of all the ‘doubtful sporocarps’ of the Aspergilli (and Sterigmatocystis of Van Tieghem), and secondly most spermatia and spermogonia. The Aspergilli show exactly the course of development of Penicillium. The doubtful sporocarps (p. 206) are bodies that look like sclerotia and resemble the perithecia of Penicillium, but differ from these, according to some observers at least, in that they show no development of asci. Brefeld’s statements® to the contrary have been silently withdrawn or ignored by himself* since the appearance of Wilhelm’s profound treatise on the subject. The question then naturally arises, what was the reason for the negative results respecting the formation of asci which were all that were obtained during so many years? Brefeld answers the question by declaring these bodies to be ‘rudimentary primordia of perithecia.’ This may be so with the bodies which Brefeld found in Aspergillus flavus and which he describes as undifferentiated tuber- like structures. But Wilhelm repeatedly obtained from A. flavus as well as from the other species a large number of well-developed bodies of the nature of sclerotia which in A. flavus had a black rind; the development therefore goes in this case also beyond the undifferentiated rudiment. These bodies in view of their structure can no more be called rudimentary than the sclerotia of Penicillium. The difference in structure which seems actually to be found in all cases, namely, that there are no distinct ascogenous hyphae such as appear in the sclerotia of Penicillium, cannot be of any importance, for this difference exists in like manner up to the commencing formation of asci between other primordial sporocarps, the perithecia of Claviceps and Pleospora for instance, on one side and those of Melanospora and others on the other. It may be allowed that these objections would be merely a playing with words, if there were sufficient grounds 1 See above, p. 122. 2 Bot. Ztg. 1876, p. 265. ® Schimmelpilze, IV, 134. CHAPTER V.—COMPARATIVE REVIEW.—ASCOMYCETES. 257 for believing that these bodies are functionless or discharge a very subordinate function. But the known facts which may be summed up in the words structure of a sclerotium and evident homology with Penicillium seem to be in favour of the contrary view, and to show that the sclerotia in question are capable of development, and are stages in the formation of ascocarps. The single argument for their being without function, and therefore, as I am prepared to allow, for their being in a rudimentary state, is to be drawn from the fact that no further development has been observed in them during the two years that they have been known, and under the conditions of cultivation which have been hitherto employed. On the other side it would be well to remember our experience with other sclerotia and resting states, to simply acknowledge our present ignorance and to give two more years to investigation before attempting to decide the question. I have purposely referred here only to Brefeld and Wilhelm. But Van Tieghem now asserts that he has actually obtained asci from Aspergillus niger, in just the same way as from Penicillium. If this is confirmed, the whole dispute is set at rest as far as that species is concerned, and the same thing will happen probably in the case of the others also. Many doubts, uncertainties, and controversies have also arisen in determining the spermogonia and spermatia. Ido not include among these the many, separate cases more or less imperfectly investigated, in which it remains uncertain whether an organ described as a spermogonium and assigned to a particular species really belongs to that species or to some other which perhaps lives as a parasite in or with the first species, and similar cases. ‘To questions of this kind we may almost always apply the remarks which will be found in a previous page respecting the determination of the genetic connection between forms occurring together, and which are really self-evident; we will only touch here on those cases in which the genetic connection of the organs in question is certainly or as good as certainly ascertained. We will fix our attention first of all on those spermatia only which are produced from spermogonia and on the spermogonia themselves, remembering always that the formation of spermatia differs in no essential point from that of acrogenously formed spores, and that the one and always recurring distinction between the two organs is that the spores germinate, while, as far as our observations go, the spermatia do not. The spores germinate by the extrusion of a germ-tube, and it has either been actually observed or it is assumed from analogy that the tube can grow into a mycelium. Tulasne, the original discoverer of the spermatia and spermogonia, suggested in the year 1851 that they were male sexual organs ; he rested his view partly on the non- germination of the spermatia, partly on the fact that their formation usually precedes that of the ascocarps, and in these points they certainly agree with the male organs of other plants. It was clear from the mutual connection of the observed facts, that it was the ascocarps and not the gonidial forms which must stand in special and direct relation to the supposed fertilisation. Beyond this no certain idea existed at the time of these first discoveries respecting the mode of fertilisation, nor was anything known of the presumptive female organ which was supposed to be fertilised. ‘The discoveries which were needed to clear up these points have been made from the year 1863 onwards. Tulasne in his first works, and others after him, had described, under the name of spermatia, some cells which resembled spermatia in their small size and in their origin, {4] S . 258 DIVISION IT.--COURSE OF DEVELOPMENT OF FUNGI. and had termed their receptacles or the organs that carried them spermogonia; but it was shown by further observation that these cells were germinating spores or gonidia, and that their receptacles should be termed gonidiophores or pycnidia, Of a similar kind were the gonidia of Claviceps and other forms mentioned in Tulasne’s Carpologia, which germinate very readily. As these observations multiplied, the question naturally arose whether there really are spermatia which are absolutely with- out the power of germination, or whether the absence of germination in the alleged cases did not arise from defects in the mode of conducting the experiments, since some spores only germinate under fixed conditions, and the conditions may not always have been properly secured in the artificial cultivation of the plants. A work of Cornu? endeavours to give an answer to this question, and a further answer is to be found in Stahl’s treatise on Collema which appeared almost at the same time. The two are very different. Stahl’s work shows that there are spermatia which are not spores but fertilising organs, and describes the mode of fertilisation and the organ to be fertilised (see above on page 211). It does this, it is true, in a limited number of cases only; but what is known of the rest of the Lichen-fungi, and is not disputed by Cornu, proves further that by far the larger part of them possess spermatia which show no more signs of germination than those of the Collemeae, and that these spermatia are homologous with those of Collema. This is sufficient to distinguish the spermatia and spermogonia from spores and their receptacles in this long series of cases, even though nothing certain is yet known as to the function of most of these spermatia. That exactly ‘ the same condition of things is to be found also outside the group of Fungi which form Lichens, is evident from the case of Polystigma described above on page 215. Cornu, on the other hand, simply does not allow that the spermatia are special organs, but would have them regarded as spores with the power of germination, while retaining the name which they have hitherto borne. His arguments for this view are not convincing. He saw first of all the ‘spermatia’ of certain species, which hitherto perhaps had been considered to be incapable of germination or had not been examined (for example those of Massaria Platani), produce germ-tubes when sown in nutrient solutions; a few more therefore to be added to the previously known cases of pseudo-spermatia. He also saw other known spermatia, those, for instance, of Stictosphaeria Hoffmanni, Tul. and Valsa ambiens, Tul., undergo changes of form, also in nutrient solutions, and swell up, but without showing further signs of germination. He gives no other new facts; the cultivation of the spermatia of Lichens gave him only negative results, and he can scarcely be said to have advanced the subject even in a single minor point. His treatise was published before the results of Stahl’s profound investigations were given to the world. From the facts which have been established we now know of spermatia or spermogonia in certain species or genera as organs with a definite function different from that of spores. We can also form a plausible view as to the homology of these bodies with the antheridial branches or functioning antheridia in other species which have no spermatia, as was attempted to be done above on page 231. Lastly, we are acquainted with a large number of species in which the homology of the spermatia 1 Reproduction d. Ascomycétes (Ann. d. sc. nat. sér.6, III) - CHAPTER V.—COMPARATIVE REVIEW,.—ASCOMFCETES. 259 and spermogonia with those first mentioned is indubitable ; but, on the other hand, we know nothing certain in almost all these latter cases about the function of the spermatia. We may certainly assume that they are male fertilising organs in all the species which possess an organ (trichogyne or ascogonium) which may be intended to be fertilised. The swelling too of the spermatia in a nutrient solution, or even the extrusion of a germ-tube, would not be an objection to this assumption, since processes of growth might make their appearance, as Stahl has already remarked, in this mode of cultivation, which in the natural course of development would only be set up after contact with the organ to be fertilised, just as pollen-tubes are formed in saccharine solutions. But, as was shown above, the female organs to be perhaps fertilised are actually known only in a comparatively small number of species, and in the rest, which are the large majority, the functions of the spermatia must therefore be declared to be doubtful. If we suppose them to*occur in species which have no female organ, they cannot there have a sexual function. Yet we can hardly call them rudimentary organs; and the enormous numbers in which they are produced are opposed to the view that they are entirely without function: their function therefore remains for the present undetermined. Supposing after what has now been said that we have satisfied ourselvés as to the distinction between spermatia and small spores, and as to the mode of naming them and their receptacles and so on, and can find our way in the practical description of them, an interesting subject of enquiry still remains in the homological relations between the two kinds of organs, for there is a striking agreement between them, not only in form and structure, but also in that which is of much greater importance, namely, the place or moment of their appearance in the course of the development. In the latter respect, for instance, the commencing small-spored pycnidium of Cucurbitaria Laburni agrees with the spermogonium of Polystigma or Physma. Here we may say, without exaggeration, that the only difference lies in the germination. In this and similar cases we only know the first products of germination, the germ- tubes; we do not know what is developed from them. We might therefore consider them to be formations which are incapable of further development, like the pollen- tubes in a saccharine solution, or we might at least enquire if they are not of this nature. However, we may put this point out of consideration and assume that they are in all cases capable of producing a mycelium. This assumption does not prevent us from maintaining their homology with true spermatia. On the contrary, we may very well conceive that we are dealing with homologues of different adaptation or metamorphosis, and this different adaptation would arise in correlation with the absence of the female organ capable of fertilisation; for, as far as we can see at present, the phenomenon in question occurs exactly in those forms which have no female organs, having lost them probably in the course of the phylo- genetic development, as we have already endeavoured to show. It is no sufficient objection that this metamorphosis of the spermatia is not found in all species that have experienced this loss, for phenomena of this kind vary continually from species to species. The hypothesis that there are such metamorphosed spermatia would make many facts more intelligible than they have hitherto been. It will depend on the results of further special investigations how far this hypothesis can be applied to small-spored S 2 260 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI, pycnidia and similar formations, and we must not here enter further into the details of the subject than the reader can at any time do for himself by comparing the examples described in the preceding pages. But we may just observe that it is possible that metamorphosis may be found in cases where it has been quite unsuspected. The hymenium which has already been repeatedly described is found on the young stroma of the Xylarieae, Claviceps, Epichloe, &c. either before or together with the first appearance of the sporocarp, and gives off small cells, which in structure, origin, and size might be spores (gonidia) or spermatia. ‘There can be no doubt that they are homologous in all these species. They were called gonidia in a previous page, because they germinate in Claviceps and Epichloe, and in Poronia and Ustulina among the Xylarieae ; but, as far as we know, they do not germinate in Xylaria—a fact which may be added here to complete our former observations on the genus. These phenomena find their explanation in the hypothesis here proposed, and may therefore be brought forward in support of it; but it is obvious that the hypothesis is not hereby made a certainty. In conclusion we must recur again to the objects which were included in page 242 under the name of doubtful spermatia. ‘The word ‘ doubtful’ must still be repeated of many of them, for we possess only brief accounts of them, and portions of these are disputed. I confine myself therefore to the cases of Sordaria, Chaetomium, and Sclerotinia, which we know more in detail through the labours of Zopf and Brefeld. Here, according to these observers, the organs in question agree as much in their characteristic development and structure as in their power of germination under the conditions to which they were submitted, and they have no other function, as far as could be ascertained, than that of spores. They are therefore organs whose function is unknown to us. It is posszb/e that they have no function at all; at any rate as they do not function as sexual or otherwise reproductive organs, they can scarcely have any important duties to fulfil, for they are usually few and small; and if the case is otherwise in the specimens of Sclerotinia tuberosa grown by Brefeld, we must not forget that in this instance the Fungus was growing under conditions quite foreign to its usual circumstances. Having regard to the known facts and to the analogies and homologies which may be applicable, there is the alternative proposed by Zopf for the determination of these bodies, that they are either functionless spermatia, or spores or gonidia not capable of germination. This is not a matter of indifference in reference to the question of the homology. But gonidia without the power of germination, according to all trustworthy data, are things which nothing but extreme necessity can allow us to assume; and in the case of the Chaetomieae, where, according to Zopf, almost every cell of the mycelium may becomea gemma or gonidium with power of germination, and in Sclerotinia Fuckeliana with its characteristic and highly reproductive gonidiophores, it would be an absurd thing that such well-furnished appliances should be occupied solely in producing sterile gonidia. But if we suppose these bodies to be homologous with spermatia, the whole matter becomes intelligible from the points of view which have now been discussed. Only one objection has been brought forward to this view. Brefeld? calls attention to the difficulty of accounting for the concurrence in ‘Sordaria’ of * Schimmelpilze, IV, p. 143. CHAPTER V.—-COMPARATIVE REVIEW,.—ASCOMYCETES, 261 spermatia with or without special functions and an antheridial branch which conjugates with the archicarp. But the ‘Sordaria’ in which the antheridial branch has been observed is Sordaria or Hypocopra fimicola described by Gilkinet, and spermatia are not said to have been found in it. The Sordarieae in which the spermatia in question have been found are different species, S. curvula, S. minuta, and others’, and it has not been shown that their young sporocarp is like that of S. fimicola. On the contrary, it has been already intimated on page 235 that there appear to be important differences in the matter of the inception of the sporocarp in the group of the Sordarieae. Brefeld’s objection therefore rests on a misconception, and is at present at least not justified ; and if it is removed, it is no longer necessary to consider at length the question of the connection between these cases and those discussed above in which the spermatia were supposed to be without sexual function. Literature of sections LIX-LXXIV. VITTADINI, Monogr. Tuberacearum, Mediolani, 1831. TULASNE, Fungi hypogaei, Paris, 1851 ;—Id., Selecta Fungorum Carpologia, I-III, Paris ;—Id., Recherches sur l’organisation des Onygena (Ann. d. sc. nat. sér. 3, I, 1844) ;—Id., Note sur lappareil reproducteur des Lichens et des Champignons (Ann. d. sc. nat. sér. 3, XV, 1851) ; see also Compt. rend..XXXII, p. 470 ;—Id., Mémoire pour servir 4 histoire organographique et physiologique des Lichens (Ann, d. sc. nat. sér. 3, XVII) ;—Id., Discomycétes (Ann. d. sc. nat. sér. 3, XX, p- 128) ;—Id., Mém. sur l’Ergot des Glumacées (Ann. d. sc. nat. sér. 3, XX, p. 5) ;— Id., Note sur l'appareil reproductive d. Hypoxylées et d. Pyrénomycétes (Ann. d. sc. nat. sér. 4, V, p. 108) ;—Id., Nouvelles obs. sur les Erysiphées (Ann. d. sc. nat. sér. 4, I, 299, and Bot. Ztg. 1853, p. 257) ;—Id., Notes sur les Isaria et les Sphaeria entomogénes (Ann. d. sc. nat. sér. 4, VIII, p. 44) ;—Id., De quelques sphéries fongicoles (Ann. d. sc. nat. sér. 4, XIII, p. 5); see also Comptes rendus, 41, p- 615 and 50, p. 16;—Id., Note sur les phénoménes de copulation dans les Champignons (Ann. d. sc. nat. sér. 5, V, p. 216). CURREY, On the fructification of certain Sphaeriaceous Fungi (Philos. Trans. Royal Soc. London, 147, 1858). DE BArY, Ueber d. Fruchtentwicklung d. Ascomyceten, Leipzig, 1863 ;—Id., Eurotium, Erysiphe, Cicinnobolus, nebst Bemerkungen ii. d. Geschlechtsorgane d. Ascomy- ceten (Beitr. z. Morph. u. Physiol. d. Pilze, III, Frankf. 1870). See also Beitr. IV, p- III. S. SCHWENDENER, Ueber d. Entw. d. Apothecien von Coenogonium (Flora, 1862, p. 224); —Id., Ueber d. Apothecia primitus aperta u. d. Entw. d. Apothecien im Allgemeinen (Flora, 1864, p. 320). FUISTING, De nonnullis Apothecii Lichenum evolvendi rationibus (Diss. inaugur. Berol., 1865) ;—Id., Zur Entwicklungsgesch. d. Pyrenomyceten (Bot. Ztg. 1867, 1868) ;—Id., Zur Entwicklungsgesch. d. Lichenen (Bot. Ztg. 1868). WORONIN, Entwicklungsgesch. d. Ascobolus pulcherrimus u. einiger Pezizen (Beitr. z. Morph. u. Phys. d. Pilze, II). Id., Sphaeria Lemaneae, Sordaria, &c. (Beitr. z. Morph. u. Phys. d. Pilze, III). JANCZEWSKI, Morph. d. Ascobolus furfuraceus (Bot. Ztg. 1871, p. 257). 1 Zopf, Chaetomium, p. 237. 262 DIVISION II-—-COURSE OF DEVELOPMENT OF FUNGI. J. KUHN in Mittheil. d. Landw. Instit. Halle, I, 1863 (Claviceps). O. BREFELD, Bot. Unters. ii. Schimmelpilze, II (Penicillium) IV. VAN TIEGHEM, Comptes rendus, 81, 1875 (Chaetomium) ;—Id., Nouvelles Observ. sur le développement du fruit, &c. des Ascomycétes (Bull. Soc. Bot. de France, 23, 1876, p. 99); see also Bot. Ztg. 1876, p. 165;—Id., Sur le dével. du fruit des Ascodesmis (Bull. Soc. Bot. de France, 23 (1876), p. 271;—Id., Nouvelles Obs. s. 1. dével. du périthéce des Chaetomium (Bull. Soc. Bot. de France, 23, 1876) ;—Id Sur le dével. de quelques Ascomycétes (Aspergillus), (Bull. Soc. Bot. de France, 24, 1877). GILKINET, Rech. s. ]. Pyrénomycétes (Sordaria), (Bull. Acad. Belg. 1874). BARANETZKI, Entw. d. Gymnoascus Reesii (Bot. Ztg. 1872). EIDAM, Beitr. z. Kenntn. d. Gymnoasceen in Cohn’s Beitr. z. Biol. III, 271 ;—Id., Z. Kenntn. d. Entw. d. Ascomyceten in Cohn’s Beitr. z. Biol. III, 377 ;—Id., Ueber Pycniden (Bot. Ztg..1877). E. STAHL, Beitr. z. Entwicklungsgesch. d. Flechten, 1, Leipzig, 1877. A. BORZI, Studii sulla sessualita degli Ascomicete (N. Giorn. Bot. Ital. X (1878), p. 43). BAINIER in Bull. Soc. Bot. de France, 25, 1878. C. FIscH, Zur Entwicklungsgesch. einiger Ascomyceten (Bot. Ztg. 1882). ' O. KIHLMAN, Zur Entwicklungsgesch. d. Ascomyceten (Pyronema, pia ar in Act. Soc. Sc. Fennicae, XIII, Helsingfors, 1883. W. Zopr, Zur Entwicklungsgesch. d. Ascomyceten (Chaetomium), (N. Act. Leopold. XLII, 1881) ;—Id., Die Conidienfriichte v. Fumago (N. Act. Leop. XL, 1878). GIBELLI e GRIFFINI, Sul polymorphismo della Pleospora herbarum (Archiv. del Laborat. di Bot. Crittogam. in Pavia, I (1873), p. 53). H. BAUKE, Zur Entwickelungsgesch. d. Ascomyceten (Bot. Ztg. 1877, 313) ;— Id., Beitr. z. Kenntn. d. Pycniden (N. Act. Leop. XX XVIII, 1876). K. WILHELM, Beitr. z. Kenntn. d. Pilzgattung Aspergillus (Diss. Berlin, 1877). O. MATTIROLO, Sullo sviluppoe sullo sclerozio della Peziza Sclerotiorum, Lib. (N. Giorn. Bot. Ital. XIV, 1882), p. 2. B. PIROTTA, Sullo sviluppo della Peziza Fuckeliana, &c. (N.Giorn. Bot. Ital. XIII, 1881), p- 130. G. KRABBE, Entw., Sprossung u. Theilung einiger Flechtenapothecien (Bot. Ztg. 1882, Nr. 5-8) ;—Id:, Morphol. u. Entwicklungsgesch. d. Cladoniaceen (Ber. d. deutsch bot. Ges. 1883). REINKE u. BERTHOLD, Die Zersetzung d. Kartoffel durch Pilze, Berlin, 1879. R. WOLFF, Beitr. z. Kenntn. d. Schmarotzerpilze (Erysiphe) in Thiel’s Landw. Jahrb. 1872 (2). M. CORNU, Reproduction d. Ascomycétes (Ann. d. sc. nat. sér. 6, 111). R. HARTIG, Wichtige Krankh. d. Waldbaiume, p. 101 (Hysterium) ;—Id., Unters aus d. Forstbot. Inst. z. Miinchen, I (Rossellinia, Nectria). W. LAUDER LINDSAY in Trans. Roy. Soc. Edinburgh, I, p. 101. (Spermogonia and *stylospores’ of Lichens.) GIBELLI, Sugli org. reprod. del gen. Verrucaria (Mem. Soc. ital. di Scienc. nat. I). A. MILLARDET in Mém. de la Soc. hist. nat. de a VI, 1868. (Myriangium, Naetrocymbe, Atichia.) See also the works quoted in the foot-notes to the text. CHAPTER V.—COMPARATIVE REVIEW.—DOUBTFUL ASCOMYCETES,. 26 3 The reader is also referred to descriptive and phytopathological literature. Nylander’s Synopsis is specially valuable among works on the Lichen-fungi; others will be found fully given in Von Krempelhuber’s Geschichte u. Literatur d. Lichenologie. DoustruL. ASCOMYCETES. Section LXXV. There are certain small groups of Fungi which, as far as we know them, show a greater amount of agreement with the Ascomycetes than with any other Fungi, and must therefore be classed with the Ascomy- cetes. Some, like the Laboul- benieae and the group formed of Exoascus and Saccharomy- ces, have asci, but are so widely separated by structure and course of development from typical Ascomycetes, that there may be some scruple about uniting them directly with this division of the Fungi; others greatly resemble certain typical Ascomycetes in all that is as- certained of their life-history, but are hitherto only known to produce peculiar small cellular bodies, ‘ bulbils,’ without power of germination, instead of spo- rocarps with asci. Tothelattercategory belong the forms Helicosporangium parasiticum, Karst., and Pa- pulaspora aspergilliformis, Eid., which have recently been described by Eidam. We can only mention them thus briefly FIG. 120. 4, d—h Stigmatomyces Baert, Peyritsch (St. Muscae, Karsten). in this place, referring the reader to Eidam’s publication; the plants themselves should be further investigated. We pro- ceed to give a short account of the other species. Most ofthe Laboulbenieae grow on the outer surface of A ripe specimen with its black organ of attachment released from the skin of the fly, showing the surface and an optical longitudinal section; the asci are seen through the wall of the perithecium. @ everywhere the appendage. 4 an isolated ascus with ripe spores. c— development of the perithecium and appendage ; successive stages of development according to the letters. ¢ two double spores fastened to the wing ofa house-fly. @, e older states on the chitinous membrane cut ~ through perpendicularly. commencement of the perithecium. g the delicate _ projection (? trichogyne) from the apex of the perithecium, with the small round swellings on the extremities of the branches of the appendage. 4 after the formation of the perithecium is completed. J full-grown specimen of Ladoulbenta Jlageliata, Peyr. from the wing-cover of Bemdbidi: li ta The stalk-like base of a second specimen is indicated, with the same black organ of attachment. @ the appendage. All the figures after Peyritsch. 4 «, g, # magn. 350, 4 d, ¢, £ 450, B 125 times. beetles which live in or near water, but some are found on other insects, as the species especially of Eastern Europe, Stigmatomyces Baeri, Peyr., which is common in Vienna on house-flies. They appear like small brushes on the surface of the insect, either singly or often, like Stigmatomyces, forming a thick fur on it. Each of these 264 DIVISION II,—COURSE OF DEVELOPMENT OF FUNGI. small brush-like bodies is a separate plant. The entire length in the largest known species, Laboulbenia Nebriae, is about 1 mm., in most species little or not more than o‘5 mm. The phenomena observed in them most nearly resemble those known in the Ascomycetes, and are named accordingly. The small plant (Fig. 120) is attached to the substratum by a filiform or clubshaped stalk, consisting usually of two cells one above the other; at the apex of the stalk is a perithecium-and a body which may be here briefly termed an appendage (a). The perithecium is narrowly conical in form or flask-shaped and in some species oblique, and consists when mature of a wall formed of a few cells disposed in two layers at the base and. one layer at the sides with a narrow orifice at the apex; the group of asci which rises erect from the base of the perithecium is closely surrounded by its wall. ‘The number of the asci and the way in which the spores are formed in them are not exactly ascertained. ‘The number of spores in an ascus is said to be 8 and 12; the ripe spores are fusiform and colourless, and being divided by a transverse wall into two equal cells are therefore compound and bicellular; they escape singly and one after another through the orifice of the perithecium, no doubt in consequence of the gelatinous deliquescence of the wall of the ascus. The appendage springs from close to the base of the perithecium in the form of a segmented hair or filament, varying, according to the species, in length and number of cells and presence or absence of branches, which in some species are very peculiar in their form and arrangement. All the cells in the mature Fungus except the asci, the spores, and the extremities of the branches of the appendage, have very thick membranes of a deep and often a dark brown colour. The Laboulbenieae have no mycelium; the ripe double spore attaches itself by one extremity to the chitinous covering of the insect, and sends into it a small short point, which sometimes enlarges into a knob at its extremity and with the surrounding chitin soon assumes a brown colour; this point is its only organ of attachment and _ of nutrition. Thus firmly planted it developes at right angles to the substratum and reaches its mature state by the necessary successive cell-divisions and differentiations. Most of the details of these formations can be seen at once in the accompanying figure for the case which it represents, but some important points have still to be cleared up. I select the following for special notice, and refer the reader to Peyritsch’s treatises for further details. The appendage is developed from the cell of the double spore which is the upper one in reference to the point of attachment; it is therefore originally terminal and is completed before the perithecium. ~The stalk and the perithecium are formed from the /ower cell of the double spore; the perithecium shoots out laterally from beneath the point which is afterwards that of insertion of the appendage, and as it increases in breadth it thrusts the appendage to oneside. In its earliest stage it is unicellular; as it grows it divides by successive transverse divisions into three tiers of one cell each, and each tier in acropetal succession then separates by longitudinal division into an axile and several parietal cells. But before the longitudinal division begins (Laboulbenia vulgaris), or before it has reached the uppermost tier-cell (Stigmatomyces), it is observed that this cell puts out a short protuberance at its apex, which is either very thin-walled or seems to have no membrane, and disappears again at a later stage of the development (Fig. 120 g, 2). Simultaneously with the formation of this protuberance on the primordium of the perithecium small thin-walled swellings are seen on the apex or CHAPTER V.—COMPARATIVE REVIEW.—DOUBTFUL ASCOMYCETES. 26 5 on the tips of the branches of the young appendage, and these also subsequently dis- appear. According to Karsten these small swellings, which are spherical in Stigmato- myces, separate in that plant from the cells on which they are formed and attach themselves to the protuberance on the young perithécium, as spermatia in the Fungi or Florideae attach themselves to the trichogyne, and then the spores or asci are developed from an axile cell. If this were so, the organs in question would have to be termed sexual organs and their homologies with the sexual organs of the Ascomy- cetes would be evident enough. But it appears from Peyritsch’s careful observations that no such supposed abscision of spermatia really takes place. We know nothing more than has been stated above, and Peyritsch himself does not think very highly of his own attempt to save the trichogyne, which might be fertilised by contact with a young branch from the appendage. It is not yet quite certainly ascertained whether the asci are formed by division or by sprouting from one or more initial cells. - With these data only to guide us, it will be best for the present to allow the remarkable little group to remain mex the Ascomycetes, being marked as doubtful, till further information is obtained concerning them. Section LXXVI. The species of Taphrina, Fr., the Exoascus of Fuckel in Sadebeck’s sense?, are parasites developing on the surface of parts of living plants, which are more or less deformed by them; Exoascus Pruni, for example, grows on the young fruit of species of Prunus, and produces swellings in them which are known as pockets, more rarely on the leafy shoots, while E. aureus is found on the leaves and ovaries of Poplars and Aspens and E. alnitorquus on the deformed fruits and upon leaves of the Alder. The Fungus when fully developed is composed chiefly of a single palisade-like layer of asci standing close beside one another, which breaks through the cuticle and covers the outer surface of the epidermis of the part attacked. The species which live on the Amygdaleae, Exoascus Pruni for example and E. deformans, develope this layer from a filiform mycelium, which first spreads in the inner parenchyma of the part and then thrusts its branches in between the outer walls of the epidermal cells and the cuticle. In this situation the branches ramify copiously, and spread out in the direction of the surface, the ramifications, which grow alongside and “between one another, forming a single layer and then becoming divided. into isodiametric cells. Each of these cells next swells into a vesicle, and breaking through the cuticle elongates in a direction perpendicular to the substratum and becomes club-shaped, and at length divides by a transverse wall into a lower cell, the short s/a/k-cell, which rests on the substratum, and an upper cell, the club- shaped ascus. The connection of the ascus-layer thus formed with the intra- matrical mycelium can be seen even when the asci are mature. Other species, Exoascus alnitorquus for instance and E. aureus, according to Sadebeck’s and to some extent also of Magnus’ earlier investigations, spread their mycelium only between the cuticle and the epidermis. Then, as the plant developes, all the hyphae become divided into ascogenous cells, and these proceed as in E. Pruni; consequently asci only are to be seen when the fructification is mature, and these are either borne on a stalk-cell (E. alnitorquus) as in E. Pruni, or have no stalk 1 In Winter, Pilze, IT. 266 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. (E. aureus). In the latter case especially and in the last-named species the outer extremity of each ascus bursts through the cuticle, while the inner extremity grows into a narrowly conical process, which becomes deeply and firmly fixed between the lateral walls of the epidermal cells. The forms of a third series, represented by Sadebeck’s Exoascus epiphyllus, which grows on Alnus incana, and E. Ulmi, also spread their hyphae between the cuticle and the wall of the epidermal cells, but form their asci from a part only of their cells, while the other part remains sterile ; hence the asci are here less crowded. The structure of the asci, the formation of the spores in them, and the ejection of the spores by mechanical contrivance, are essentially the same, as far as is at present known, as in other organs of the same name. The number of the simultaneously formed ascospores is also usually eight in Exoascus Pruni; other numbers will be mentioned further on. All the spores are small, simple, ellipsoidal cells with a delicate colourless membrane. The spores of Exoascus Pruni are ejected when ripe and germinate at once in water or a nutrient solution, sprouting repeatedly and perfectly and forming many orders of sprouts. Those of the first orders are of much the same shape and size as the mother-spore, those of the higher are often much smaller. If the ripe spores are detained in the ascus, they often form their germ-sprouts in it, and the ascus becomes filled with countless sprouts of different orders and sizes, which readily separate from one another and escape as individual ‘spores’ when the ascus opens. The spores germinate in a very similar manner in the other species. In many of them, those for instance which live on Poplars and Alders, a very large number of small sprouting spores are found in the ripe ascus. Sadebeck states that these are always sproutings from eight primary ascospores; according to my earlier researches and Brefeld’s investigations, repeated quite recently, the original spores in Exoascus Populi may be less than eight; Brefeld says that there are usually four, and I remember to have seen only two and three. Short germ-tubes, which soon give -off sprout-cells, are occasionally formed from the spores,‘ as, for example, in E. alnitorquus. Sadebeck has noticed that the products of the germination of the spores of. - Exoascus alnitorquus and E. bullatus penetrate into young leaves of Alnus glutinosa or Pyrus communis, and there develope directly into ascogenous hyphae. The mode of penetration is not stated. This observation would justify our assuming a similar behaviour in the other species, with the addition that in some of them at least the mycelium vegetates and maintains itself for a long time in the plant which it attacks, For instance, it is found early in spring in the rind of the branches of Prunus and © spreads from them into the young twigs and fruits; and in E. deformans, which inhabits the cherry-tree, it is perennial and lives for years in the rind of the branches, where it causes the ‘ witches’ brooms,’ and sends branches every year to form asci in the leaves, which are disfigured in a similar manner. There is another doubtful Fungus which Reess has named Endomyces decipiens, and which must for the present be placed near Exoascus. It grows in old lamellae of Agaricus melleus and consists of septate hyphae, which are often constricted at the septa and produce small ellipsoid asci arranged in lateral clusters. CHAPTER V.—COMPARATIVE REVIEW.—DOUBTFUL ASCOMYCETES. 267 Four hemispherical spores are formed in each ascus, which escape when mature by the dissolution of the wall of the ascus, and put out germ-tubes in water. Nothing more is known of this species; the controversy which has arisen in the attempt to determine it will be noticed again in section XCIII. Section LXXVII. The chief representatives of the genus Saccharomyces are the Yeast-fungi which excite alcoholic fermentation and are known as Sac- charomyces Cerevisiae, S. ellipsoideus, S. Pastorianus, &c.. These names, according to E. Hansen’s recent investigations, denote form-groups, which will no doubt have to be otherwise distributed. Besides these there are the Flowers of wine, S. Myco- derma, Reess, Cienkowski’s Chalara Mycoderma, and the Fungus of thrush (apthae), S. albicans, Reess, which grows as a parasite on the mucous membrane of the human digestive organs, but also thrives in saccharine fluids, where it excites a slight fermentation. The rest are found in quantity in or on fluids which are fermenting or have undergone fermentation. S, Cerevisiae is added intentionally to the wort of beer and is cultivated largely for this purpose. Other kinds and indeed S. Cerevisiae as well appear of themselves in must, finding their way into it chiefly from the surface of the juicy fruits which yield the must. " They are conveyed to these fruits along with zs dust from the surfaces of other bodies (see be- @°Q low, section C). @ The larger part of these Fungi vegetate, as far as we know, only by sprouting (Fig. 121). Continuous branching hyphae with long seg- ments are found only in Saccharomyces albicans, in S. Mycoderma and Cienkowski’s 2 Chalara; these grow directly, according to Cienkowski’s observations on S. Mycoderma, ee ees eee from cells formed by sprouting, produce fresh solution. Successive stages of development according to the letters. Magn. 390 times. cells from their sides by sprouting, and ulti- mately divide transversely into short cells which then vegetate simply by sprouting. Other species, especially Reess’ S. Pastorianus, show a certain approach to this growth-form in that they are frequently chains of elongated sprout-cells, from which short cells are abscised laterally. ‘The shape moreover of the single sprout varies generally between spherical and elongated cylindrical, with certain rules and limitations in each species. The cells that are formed one after another by sprouting in the fermenting fluid are usually at once separated from one another; connected strings of cells are to be seen when the plant vegetates on still surfaces, such as a microscopic slide especially, and the length and number of the chains vary according to the species. The cells of S. Cerevisiae, when developed in large quantities, often adhere together irregularly and form largish lumps, being attached to one another apparently by the muci- laginous outer lamellae of their membranes (see on page 9). The structure of the sprout-cells is that of other vegetative fungal cells, but their membranes are comparatively thin and colourless. The Saccharomycetes in the sprouting form may be said to be capable of unlimited growth and multiplication if supplied with sufficient food. This is shown by the hundreds of thousands of pounds weight of yeast which are produced year by 268 DIVISION II.—COURSE OF DEVELOPMENT OF FUNGI. year and which consist entirely of the sprouts of S. Cerevisiae. But a certain number of known species also forms spores 7m asc¢ under certain conditions; this fact was dis- covered by De Seynes in Saccharomyces Mycodermain, 1868, was afterwards examined more thoroughly especially by Reess, and has now been certainly established in S. Mycoderma and the forms included under the names of S. Cerevisiae, S. ellipsoideus and S. Pastorianus. It occurs most readily and most frequently in thesS. ellipsoideus of wine-yeast. It has been studied by Reess, Hansen, and other observers in S. Cerevisiae, but it is often difficult to induce this cultivated form to produce spores. Spores begin to be formed if well-fed specimens, protected as far as possible from invasion by other Fungi and Schizomycetes, are kept without food or restricted to the least possible amount of it in presence of water and air containing free oxygen and in a suitable temperature ; if, for example, yeast is spread in a thin layer on moist surfaces, such as succulent parts of plants, plaster of Paris, or a microscopic slide, or kept in a little distilled water. At first new cells are formed by sprouting in such cultures at the expense of the old ones, which may become exhausted and sometimes die. Then spores are formed in cells which are not distinguished by their origin, shape, or any other particular, sometimes in a few isolated cells, at other times in all or most of the cells of a chain. Two or four, or some- times three, seldom more than four spores are formed in a cell according to its size. The stages observed in the formation of the spores correspond to the processes known to occur in asci (see section XIX). The young spores appear simultaneously as delicately circumscribed round bodies of homogeneous protoplasm collected into a group inside the protoplasm of the mother-cell, in FiG.122. Saccharomycesellipsoideus, Which a parietal layer of protoplasm remains at first R. (Wine-yeast). Formation of spores 4 in sprout-cells, taken from ferment- @verywhere unbroken (Fig..122). The spores soon form ing must and spread out for thirty- ; A : 3 six hours on a microscopic slide in dis) @ Membrane which always remains thin, and increase fully formed. Magn about 60times, in volume while the protoplasm more or less completely disappears. When full-grown they may just fill the cavity of the mother-cell, but generally they do not quite fill it; if they are four in number they are disposed tetrahedrally as quadrants of a sphere or in a row according to the shape of the cell. They are now arrived at maturity. In older specimens the membrane of the mother-cell often collapses and disappears ; it is ruptured according to Cienkowski’s account in Saccharomyces Mycoderma and releases the spores. The ripe spores can germinate as soon as they enter the nutrient fluid. In germination they swell slightly and form vacuoles, and then begin to sprout in the manner proper to each species ; the membrane of the mother-cell is broken through as the first sprouts are extruded. E. Hansen found in the species which he examined sprout-cells which were - divided by thick flat partition-walls into 2-4 daughter-cells, and these cells germinated in the same way as the ascogenous spores, but he did not see the formation of these septa. Meanwhile, judging from the figures, we should be inclined to suspect that the formations in question are simply asci with their walls much collapsed after ripening and with the spores closely pressed one against another. The foregoing brief account of the formation of the spores of the Saccharomycetes is taken from Reess’ earlier statements and a recent revision of them in examining CHAPTER V.—COMPARATIVE REVIEW.—DOUBTFUL ASCOMYCETES. 269 Saccharomyces ellipsoideus; it would appear to be an evident case of partial division or free cell-formation (see page 61), in which the observed facts perfectly correspond to what is known of, the formation of spores in smaller asci (Exoascus, Eurotium). The term asci.is accordingly chosen or retained. It is true that there are differences of opinion with regard to the process in question. Cienkowski suspects that in S. Mycoderma the whole of the protoplasm of the mother-cell is divided into spores, and Brefeld speaks in the same way as regards other species, (‘ wine-yeast’) in so far as he considers the sporogenous process in Saccharomyces to be like that in Mucor, regarding the latter indeed as a case of partial division. It is otherwise in the Saccharomycetes examined by Reess and myself. The continued presence of the parietal layer of protoplasm after the formation of the spores is decisive in their case even now, when the distinction between ‘free cell-formation’ and (total) division is less sharp than it once was. The spores are not formed in the sporangia of Mucor in the same way as in Saccharomyces (see page 74). Lastly, Van Tieghem has proposed a view which differs entirely from any other’. He thinks that the spores of Saccharomyces are produced by the division of the whole of the protoplasm, but that they are pathological formations induced by the assaults of Bacteria ; this idea. was suggested by the behaviour of spores of Mucor in presence of Bacteria, but it is at once refuted by the observation of a good specimen grown beneath the microscope in distilled water and free from Bacteria, and appears to have been recently abandoned by its author”, . Section LXXVIII. There can be no doubt, from what we know of the history of development in the ascogenous Saccharomycetes, that they are immediately connected morphologically with the Exoasci. The differences in form between them and the Exoasci, whose hyphae are broken up into asci, would even allow of the two groups being united into one genus. The two genera therefore together form a natural group, which may be called here the Exoascus-group. If we enquire further into the connection of this group with other Fungi, we can only take morphological arguments into consideration in determining the question. No decisive argument of the kind is to be drawn from the simple vegetative structure ; the tendency to vegetate by sprouting or the actual occurrence of this mode of vege- tation in Saccharomyces cannot determine anything, for this phenomenon occurs in the most heterogeneous fungal groups, as has been already pointed out and will be again noticed below. But our group forms asci, and this peculiarity it shares only with the Ascomycetes, if we disregard Protomyces, which, however, is much further removed from it (see p. 171), and this must be decisive at present for its connection with the Ascomycetes. Brefeld’s early opinion, expressed in the year 1876, that Saccharomyces belongs to the Mucorini was disposed of when it was shown that the chief argument in its favour drawn from the similarity in the mode of spore- formation cannot be maintained. The connection with the Ascomycetes rests entirely on the resemblances which have been pointed out between the two groups. It remains uncertain how far these resemblances are the expression of natural and phylogenetic affinity. That they are the results of such an affinity is rendered highly probable by the great agreement between the hymenia of the more highly differentiated Exoasci and typical Ascomy- ' Ann. d. sc. nat. sér. 6, IV, p. 9. * Traité de Botanique. 270 DIVISION II,—-COURSE OF DEVELOPMENT OF FUNGI. ‘ cetes. Objections to this view are drawn from the entire absence of archicarp and ascogonium and differentiation of ascus-apparatus and envelope-apparatus. But we have constantly seen variations in the amount “of differentiation in these organs within the group of the Ascomycetes, and can therefore conceive of an extreme simplification; we must perhaps wait for the discovery of more thoroughly inter- mediate forms. If without waiting for more exact proof we assume a phylogenetic connection between the Exoascus-group and the Ascomycetes, two views are open to our adoption. Either the former group represents the simple s/arfing-point of the series of Ascomycetes, the Saccharomycetes containing the simplest forms from which Ascomycetes have been gradually developed; or its members are greatly reduced Ascomycetes (see page 125), with extensively interrupted homology which is only restored with the appearance of the asci. The latter is the only admissible assump- tion if the account given above of the relation of the Ascomycetes to the Phycomycetes by affinity and descent is the true one, and it must be maintained with the necessary reservation so long as these relations, which are the natural conclusion from known facts, are not set aside by the discovery of new ones. Most of the species of Saecharomyces which have been mentioned above are the most common and practically the most important inciters of alcoholic fermentation ; they are the yeasts of fermentation and are for this reason generally termed Yeast- fungi. Some of them, beer-yeast for example, are purposely added to the liquid which is intended to ferment; the juices of certain fruits ferment spontaneously, the yeast-plants appearing in them without artificial assistance. This led the earlier observers to the notion, which afterwards reappeared from time to time, that the Yeast-fungi are formed without parentage from the organisable material contained in the juices of fruit. Karsten’ in 1848 derived them from organised ‘vesicles,’ which had been normal parts of the cells of living plants and continued to vegetate inde- pendently after their death. But ideas of this kind have been given up for many years. We now know that the Yeast-fungi are derived from parent-forms as members of the development of a normal species of Fungus, and that their germs find their way from without into fermentable fluids ; this latter point will be noticed again in a subsequent chapter. But those who upheld this view carried on a lively controversy respecting the systematic or morphological relations of the Yeast-fungi, especially before the asci of Saccharomyces had been observed by De Seynes and Reess in 1868 and 1870. Some writers regarded them as independent representatives of distinct species which always appear in the form of. sprouting Fungi (Schwann, Pasteur, De Bary). Others, on the contrary, considered them to be special forms of species of Fungi which are generated in suitable fluids, and which appear in some other form, chiefly that of the Hyphomycetes, outside these fluids; they thought that the characteristic sprouting form of the plants and the yeast-fermentation depended on the nature of the medium, and that the Fungus could be brought back again to the other form, the Hyphomycetous form for example, by changing the medium. Either some particular species were indicated as capable of this transmutation, chiefly the common Moulds, species of Mucor for example, Sclerotinia Fuckeliana (Botrytis cinerea) (Bail) or Penicillium (Berkeley), or the capacity was supposed to exist in a great variety of Fungi, though here again the commonly diffused species just named stood at the head of the list (H. Hoffmann). . Continued investigations have brought to light the reasons for this variety of ? Bot. Ztg. 1848, p. 457- CHAPTER V.—COMPARATIVE REVIEW.—DOUBTFUL ASCOMYCETES. 271 opinion. They have shown that the earlier observers obtained uncertain results from having different and imperfectly distinguished forms mixed up together in their impure cultures, and have revealed another source of obscurity in their belief that every form of sprouting Fungus must be regarded as an inciter of fermentation or ‘Yeast-fungus,’ and conversely that all alcoholic fermentation was caused by the vegetation of a sprouting Fungus resembling Saccharomyces. We know now that this is not so. “But there are firs¢ of all many species of Fungi in which the only mode of vegetation is by sprouting or which vegetate in this way under certain circumstances or in certain stages of their development. Foremost among these are the ascogenous species of Saccharomyces. Connected with the latter are the forms which resemble them exactly in their vegetative construction, but in which asci and distinct spores are not known, or it should be said perhaps are not ye¢ known. These are usually, and for the present rightly placed in the genus Saccharomyces ; whether they really belong to it has yet to be ascertained; among them are S. apiculatus which has been so thoroughly examined by E. Hansen, and ‘Pasteur’s Torulae’ recently investi- gated by the same observer. To these must be added Exoascus, also the plants mentioned above on page 114 as examples of germination by sprouting, and certain Mucorini (see page 155) with further in- stances in the Ustilagineae (see page 179), Tremellineae, and Exobasidium recently A supplied by Brefeld (see section XCII). Lastly, we must mention Fumago, (see page 249) on Zopf’s authority, and a form most probably nearly related to Fumago a : a0) or Pleospora and at present imperfectly known, which I formerly described as x Dematium pullulans. It is very com- mon on the surface of plants; and for this reason and because its sprout-cells are very like those of some species of Saccharomyces the two forms have no doubt often been mistaken for one another : ; z < 7 “pee IG. 123. Dematium pullulans. A, x x portion of a row by earlier observers, who did not distin- — ofcells with brown membranes forming tubes and occasionally . : . sprouts in a saccharine solution. 2 portion of a filament guish different forms very acutely. It 1S vegetating in a saccharine solution and covered with sprout- probable that a similar confusion is at the “ 358 DIVISION III..-MODE OF LIFE OF THE FUNGI. Saccharomyces which excite fermentation, but the forms or species of which he does not determine, are found in abundance at harvest time on grapes and on their stalks, while they are rarely or never found at a later time on grapes which have remained through the winter and on young grapes in summer; this means that those cells which may happen to have survived have at least become incapable of development. Few saprophytic Fungi are known to be specific ferment-organisms, if we judge of them by their effect on the substratum. Several species of Saccharomyces are the Yeast-fungi of alcoholic fermentation, and near them come species of Mucor which produce a similar kind of fermentation. The power of producing fermentation is a specific peculiarity, as has already been pointed out on page 271, and not confined to any particular growth-form, as that of the Sprouting Fungi for example. It is wanting among the Saccharomycetes in the flowers of wine, Saccharomyces Mycoderma or mesentericus, and perhaps in some others; it varies in the forms which excite fermen- tation according to the species, all other conditions being the same. Of the Mucorini, Mucor racemosus, M. circinelloides, and M. spinosus cause a tolerably active fermen- tation in the sugar, while the activity of M. Mucedo is small, and that of M. stolonifer is scarcely greater’. Wan Tieghem? showed that the mycelium of Penicillium and of Aspergillus niger when growing in sclution of tannin breaks up the tannin into gallic acid and glycose. The ferment-secretions have already been noticed on page 355. It is almost certain that further investigations will show tne existence of fermenting power in other saprophytic Fungi. It is known that the final result of the process of vegetation in most of the saprophytes which have been examined is a combustion of the organic. substratum. . Penicillium also and Aspergillus niger cause combustion of the tannin when they vegetate on the surface of the solution with an unlimited supply of oxygen. 4. PARASITES. Section CI. We have little exact knowledge of the chemico-physiological pro- cesses in the life of the parasitic Fungi, because the symbiotic relation puts great complications and difficulties in the way of their precise investigation. We encounter on the other hand in these Fungi a very long and varied series of phenomena of one-sided or reciprocal adaptation between the parasite and the. living organism on which it feeds, and some of these phenomena are of a very. obvious character. In contemplating them we have to set out from the following general considerations. The plant or animal on which a parasite lives is termed its hos¢ or feeder. Every parasite species lives on certain host-species, and the limits within which it can choose its host are different in different species. Some parasites have never been ob- served on more than a single host, Peronospora Radii for example on Pyrethrum ino- dorum, Uromyces tuberculatus on Euphorbia exigua; so Cystopus Portulacae, Rhytisma Andromedae, Triphragmium Ulmariae and T. echinatum, and many other species that 1 Brefeld, Ueber Gahrung, as cited on page 188.—Gayon. in Comptes remdnts 86 (1878), p. 52, and in Ann. Chim. et. Phys. XIV (1878), p. 258. ? Ann. d. sc. nat. sér. 5, VIII (1867), p. 210. CHAPTER VII.—PHENOMENA OF VEGETATION. —PARASITES. 359 are parasitic on plants; of parasites on animals Laboulbenia Baeri is found only on house-flies. Very many kinds thrive on a larger or smaller circle of nearly allied species which serve them as hosts; among these are many Uredineae, Ustilagineae, and Peronosporeae, Epichloe typhina which lives on the Gramineae and Claviceps purpurea; Cordyceps militaris grows on insects of various orders, especially Lepidoptera ; C. cinerea, as far as is known, only on species of Carabus, other kinds only on wasps, and so on. Some kinds make specific exceptions within the immediate circle of affinity of their host, or they occasionally travel beyond that circle; I succeeded for instance in transferring Puccinia suaveolens, which usually lives on Cirsium arvense and Centaurea Cyanus, to Taraxacum but not to Tragopogon ; Phytophthora infestans, which is usually confined to the Solanaceae, is found excep tionally on the Scrophularineae (Anthocercis viscosa, Schizanthus Grahami), Perono- spora parasitica of the Cruciferae on Reseda luteola. This exceptional power of accommodation forms the passage to the third category, that is, to parasites which attack plants and animals of very different cycles of affinity either without any distinction whatever or with a preference for certain species. Examples of parasites of this kind living on plants are species of Erysiphe, as E. guttata which lives on the leaves of Corylus, Carpinus, Fagus, Betula, Fraxinus, and Crataegus, Phytophthora omnivora which attacks Fagus, Sempervivum, the Oenothereae and other plants, but not Solanum tuberosum’, and Sclerotinia Sclerotiorum, which can penetrate as a parasite into the most diverse juicy parts of plants. Of cases of parasites on warm-blooded animals may be mentioned Lichtheim’s Mucor rhizopodi- formis, one of the pathogenous Moulds which will not develope on the dog, but grows, vigorously in the rabbit; Aspergillus fumigatus attacks both of these animals; no others have been tried. For further examples the reader is referred to descriptive and pathological treatises. These facts and gradations would lead us to expect that there must also be differences in the aggressive behaviour of a parasite to the different varieties and in- dividuals of a host; or, to express the matter in the converse way, in the predisposition of the individuals for the attacks of the parasite. In this direction also there are all possible gradations. On the one hand there are parasites which, as far as we know, show no preferences of the kind, for instance all the strictly parasitic species of the genus Peronospora and of the group of the Uredineae in which this point has been examined. The other extreme is represented by the Saprolegnieae for example, which. attack fishes, and by the Sclerotinieae and Pythieae, which as facultative parasites attack Phanerogams. ‘These will be discussed at greater length in a suc- ceeding page (see p. 380). The physiological reason for these predispositions cannot in most cases be exactly stated; but it may be said in general terms to lie in the material composition of the host, and therefore to be indirectly dependent on the nature of its food. In the case of the Pythieae, for example, it is easy to see that the host displays degrees of susceptibility or power of resistance in presence of the parasite proportioned to the amount of water which it contains*. It must on the whole be 1 Bot. Ztg. 1881, p. 595. ? On the disposition of plants see Sorauer, Landw. Versuchsstationen, XXV (1880), p. 327, and the discussion in Bot. Ztg. 1882, pp. 711 and 818. The questions :of disposition and immunity in the case of diseases of animals caused by parasites are fully discussed in medical literature. + 360 DIVISION III.—MODE OF LIFE OF THE FUNGI. conceded that a predisposition for the attack of a parasite may in some cases be a sickly one, especially if there are deviations at the same time from the condition which we are accustomed from experience to consider the healthy condition in the particular species. But it is also evident, on the other hand, that the predisposition to the attacks of parasites does not always show a sickly condition of the plant, not for instance when there is no parasite present. The real state of things must be investi- gated and determined case by case. It was shown by many examples in the morphological portion of this work, that the parasite is either an endophy/e and lives inside the organs or even the cells of the host, or is to a great extent an epzphy/e on its outer surface. A purely epiphytic mode of life, in which the parasite rests on or is attached to the outer surface of the host, is comparatively rare if we disregard the case of the Lichen-fungi to be described in section CXV ; the Laboulbenieae (page 263) and Melanospora parasitica’ and perhaps also those’ Chytridieae which are said only to rest on their host may be mentioned as examples of this kind. Other epiphytes, as Erysiphe, Piptocephalis, and Syn- cephalis, enter the interior of the host at least by the haustoria which they send into it. .Chaetocladium adhering to its host and with its tubes in open communication with those of the Mucor which serves as its host does not strictly come into either of the two categories (see on page 20). Either designation may be applied to the Fungi which spread in the deric tissues of the higher animals. After these preliminary remarks we may proceed to consider the phenomena of adaptation above indicated under three general heads: 1. The aéfack of the parastte on its host, that is, the first beginning of the occupation. 2. The course taken after occupation by the further growth of the parasite. 3. The reactions of the host after its occupation and the results of the reciprocal action of the two symbionts, It is owing to the nature of the subject-matter, that though the three questions are kept theoretically distinct from one another, the answers to them must necessarily travel out of the domain of one question into that of another, and especially from the second to the third. Section CII. The parasitic Fungus attacks its host by means of its spores, or of the germ-tubes emitted by the spores, or of the hyphae developed from the germ-tubes. The first case, in which the first attack is made by the spore before germination, is confined to a comparatively small number of epiphytic species, which will be noticed again in another connection at the conclusion of the paragraph, and to certain facultatively parasitic and facultatively endophytic species of Moulds, namely, the pathogenous Aspergilli and Mucor-forms (M. rhizopodiformis and M. corymbifer) which have been studied by Lichtheim*. These Fungi are developed in the internal organs of warm-blooded animals, when their spores find their way into the blood- passages and are carried by the blood to suitable spots; wounded places therefore, though of very small extent, are always in the natural course of things the parts where the endophytically developed Fungus first makes its attack. ‘These forms are actually known as true endophytes only from artificial injection usually of a large number of ' O. Kihlman, as cited on page 262. ? As cited on page 349, and in Zeitschr., f. deli Medicin, VII, Heft 2. CHAPTER VII.—PHENOMENA OF VEGETATION.—PARASITES. 365 ‘spores; they appear in nature rather as epiphytic growths on the walls of cavities’ in the bodies of animals which are oars accessible from without, such as the cg of the ear and the bronchi. In most cases the spore of the parasite begins the emission of a germ-tube independently of the host, either after simple absorption of water or by appropriation at the same time of food-material produced outside the host. If the tubes or the hyphae which proceed from them then come into contact with the host, they fasten upon it in the way peculiar to each species. The most common case of the kind is when the spore finds its way by some mode of dissemination or other to the surface of the body of the plant or animal, and puts out germ-tubes which penetrate into the body. Parasites which, like Ancylistes Closterii and Polyphagus Euglaenae, attack unicellular organisms living in societies, send out mycelial branches from the individual first attacked, and these can fasten upon fresh individuals and by degrees on entire aggregates of the host-cells. Some facultative parasites of higher or- ganisms, Sclerotinia for example, Agaricus melleus and others of R. Hartig’s tree-destroying species, behave in the same manner, since any of the hyphae or mycelial strands are able to make their way into new individual hosts. The act of penetration is accomplished in two way 8; the FIG. 163. Uromyces appendiculatus. a uredospores germinating in water. at "CrRn 6 uredospores which have germinated on the epidermis of Fada vulgaris, the germ tube or branch of the my ce germ-tube penetratinginto astoma, c¢ germ-tube which has passed through the lium either grows into the interior soestnsse pocmcsyes ofa nett ets wd tere ened con mie of the host through a natural = pom 6 the germ-tube which is outside the leaf not being shown. Magn. - opening in it, or it pierces through the firm membranes of the surface of the body of the host. The one or the other mode is adopted according to the species and the kind of spore; it is seldom that both occur promiscuously, Many examples of the first kind are supplied by those endophytic parasites on plants, in which the germ-tubes ex/er the host by the stomata only. All the uredo- spores and aecidiospores of the Uredineae for instance germinate on the moist epidermis of phanerogamous plants. ‘The germ-tube grows in a curve on the surface of the epidermis, and when its tip reaches a stoma it descends into it, usually after it has first become vesicularly swollen outside the stoma, and then passes on into the air-space which lies beneath it. Here it increases rapidly in size and receives the entire protoplasm of the germ-tube, while the rest of the germ-tube outside the spore- membrane dies away. The extremity of the tube which has thus penetrated into the host can now put forth branches which develope into mycelial hyphae (Fig. 163). These germ-tubes enter the stomata of any phanerogam, but only develope further in the species which is the proper host of the particular parasite ; they wither away in all other species in the subepidermal air-space. The short germ-tubes from the sporidia of Leptopuccinia Dianthi, DC. proceed in a similar manner. If a sporidium of this plant germinates in the neighbourhood of a stoma of the host, its germ-tube grows 362 ; DIVISION III.—MODE OF LIFE OF THE FUNGI. towards it, enters it and developes into a mycelium. If germination, which occurs readily everywhere in a damp atmosphere, takes place on some other substance, the tubes grow irregularly in every direction and perish after a short increase in length. The entry through the stomata has been observed also in species of Entyloma? and Kuhn’s Polydesmus exitiosus?. Further instances will be found in pathological literature. Among endophytic parasites on animals I mention here the germ-tubes of the aerial gonidia of Cordyceps militaris (‘ Isaria farinosa’), which I only saw enter the | stigmata of caterpillars on which they had developed from the germinating spores *; but this observation requires to be revised. The second case in which the germ-tubes or hyphae pierce through the firm membranes of the uninjured host is probably the more common. It is of course the form which occurs in all endophytes on unicellular organisms. Examples of it are seen in the case of parasites on higher plants in the germ-tubes from the sporidia of the Uredineae, excepting always Leptopuccinia Dianthi just mentioned, and in those of most of the Peronosporeae and Ustilagineae*; Polystigma rubrum® together with many other Pyrenomycetes and Discomycetes, Claviceps also and the facultatively parasitic Sclerotinieae (see section CVIII) may be added to the list. It is to be particularly observed that the germ-tubes of these parasites on higher plants ever penetrate into the host by a stoma. Even if the spore lies on or near a stoma, the germ-tube either pierces through a guard-cell, or crosses the cleft as it grows and pierces the wall of an adjacent cell. The germ-tubes of most of the insect-killing Cordyceps, Botrytis. Bassii, and the Entomophthoreae belong to this class; their tubes pierce through the chitinous skin of the body of the host, and may begin to ramify in the substance of the thick chitinous skin of the larger caterpillars, Some parasites on plants show both modes of proceeding, for the same germ- tubes may penetrate through the stomata and through the membrane of epidermal — cells; this is the case in Peronospora parasitica, Phytophthora infestans, and Exoba- sidium Vaccinii*®; species also of the mode of life of Sclerotinieae can enter the host by the stomata. Finally, there are a certain number of parasites whose germ-tubes and hyphae penetrate into woody plants, not through uninjured surfaces, but where some wound has been received, and from thence make their way into open spaces, such as injured vessels (Nectria cinnabarina), or pierce through the cell-membranes. This is the case with most of the tree-destroying Hymenomycetes studied by Hartig, with Peziza Will- kommii and the species of Nectria which are parasites on trees. See section CVIII. From this series of phenomena which constitutes the general rule deviations occur in two directions, but the deviations are connected with the rule by intermediate forms. One of these deviations is found chiefly in endophytes which vegetate intracellu-~ ? Bot. Ztg. 1874, pp. 93, 103. ® Krankheiten d. Culturgewiichse, p. 152. * Bot. Ztg. 1869, p. 590. ~* Wolff, as cited on page 185: —Kiihn, ‘in Sitegbr. d. Naturf. Ges. Halle, 24 Jan. 1876. * Fisch, in Bot. -Ztg. 1883, p. 851. -®§ Woronin, as cited on page 341. -- ~~: + Raed CHAPTER VII,-—PHENOMENA OF VEGETATION,— PARASITES, 36 3 larly, and consists in extreme cases in this, that germination does not take place independently of the host, but only when the spore capable of germination has reached the surface of the proper host. When it has done this it at once puts out a germ-tube at the point of contact which penetrates directly through the membrane, otherwise it perishes without germinating. This is the history of many Chytridieae, Synchytrium especially, which are entirely or partially intracellular in their vegeta- tion, of Completoria’ also, and, as it appears, of Protomyces macrosporus. This mode of penetration is also the normal one in some Chytridieae and Pythieae, though they are able also to put out small short-lived germ-tubes without contact with the surface of the host. A quite peculiar mode of proceeding, but approaching the above, has been observed in the swarm-spores of Cystopus and Peronospora nivea (Umbelliferarum) ; these spores put out germ-tubes in water which soon die away ; in drops of water on the surface of their host they come to rest usually on or close to the stomata of the latter and send their germ-tubes into them and then proceed with their further development. The other deviation from the general rule is observed in epiphytic parasites on plants, which continue their chief growth outside. the host during the whole of their life, but send haustoria into its cells. Here the spores form germ-tubes independently of the host, but where the tubes are in contact with a cell of the host, they send out peculiarly shaped branches, which pierce through the wall of the cell and develope into haustoria. In the Mucorini, which are more or less facultatively epiphytic (Piptocephalis, Syncephalis, &c.), a copious formation of mycelium and gonidia may take place independently of the host if sufficient food is supplied to the plant. The germ-tubes of the Erysipheae*, after a short increase in length, send a haustorium at once into an epidermal cell of the host and develope on the food thus supplied to them from it into mycelial hyphae, which successively form new haustoria similar to the first. If the young germ-tube does not encounter the epidermis of a suitable host it dies after a slight elongation. When the germ-tube penetrates through a membrane, which usually happens after it has grown for a short time in some other direction, its extremity bends round towards the wall which is to be pierced, presses upon it and then grows transversely or obliquely through it. In doing this it may maintain nearly the same breadth in the perforated membrane as it had outside it, or it may be considerably narrowed and contracted. But in certain cases, as for example in the sporidia of the Uredineae, the portion of the tube which passes through the outer wall of the epidermal cell is a very slender process, usually appearing only like a simple line even when highly magnified ; as soon as this process has entered the cavity of the cell its tip swells at first into a roundish and then into an elongated tube-like vesicle, and the entire protoplasmic content of the spore streams into it; the spore itself and the portion of the germ-tube which is outside the epidermis of the host are seen to be filled only with a watery fluid and soon disappear. ‘The filiform process also which passes through the cell-wall then becomes indistinguishable, and the opening which it produced in the wall appears to become closed up again; in a short time after the 1 Leitgeb as cited on page 160, ? De Bary, Beitr., and Wolff, Beitr., as cited on pages 261, 262. See also Fig. 6. 364 DIVISION III.—-MODE OF LIFE OF THE FUNGI. perforation of the wall every trace of the proceeding has disappeared with the exception of a small projection which attaches the tube within the cell to the place of entrance. The tube now grows and ramifies inside the epidermal cell, and ultimately pierces through the inner wall of the cell and developes a ae in the tissue beneath it (Fig. 164). The majority of the intracellular Chytridieae, especially the Synchytrieae, show the same extremely slender perforating process, the same transference of the protoplasm of the spore, and the same ultimate disappearance of the wall of the empty spore and the perforating process. In some species the penetration begins with an indentation in the membrane, which must be accompanied with a corresponding local extension of the surface; the indentation forms a sheath of a certain depth round the tube, and is _ subsequently pierced at the apex, showing sometimes characteristic struc- tural peculiarities. This is the process in the case of Leitgeb’s Completoria (see page 160), Peronospora Radii and some other species. The above phenomena of penetration on the part of germ-tubes and haustoria take place only in the membranes of the host which happen to be suitable to the parasite. FIG. 164. @ Uromyces appendiculatus, Sporidia germinating on the epidermis The germ-tubes when Pp laced . of the stem of Faba vulgaris, Mch.; the germ-tube of one sporidium x has pene- On other species usually perish trated into a cell of the epidermis and grown considerably. 5 Phytophthora infes- tans; zoospore germinating and germ-tube penetrating into an epidermal cell (cut without penetrating into the through transversely) of the stem of a potato. The preparation made seventeen hours after the dissemination of the spores. Magn. 390 times. cells. I have only once ob- served an exception to this rule ; ; in this case the germ-tubes of Peronospora pygmaea, Ung. which lives on species of Anemone penetrated into the epidermal cells of Ficaria ranunculoides, but died away there at once. The thickness or other structural characters of the membranes of the host, which vary at different ages and in different individuals, are in most cases of little moment, though young and delicate membranes are more easily and more rapidly pierced than those which are strongly thickened. In certain cases, however, perforation is possible only in certain states of development of the membranes of the host, and these states have some relation to the age. The Synchytrieae for example only penetrate into the epidermal cells of young leaves of their host which are not fully unfolded; the sporidial germ-tubes of Endophyllum: Euphorbiae only into the epidermal cells of the young foliage of Euphorbia amyg=. daloides which are formed in the same summer with themselves, not into the leaves of the previous year which have gone through the. winter; and MARY Ustilagineae only into parts of young germinating host-plants, CHAPTER VII-—PHENOMENA OF VEGETATION.—PARASITES. 365 In some endophytes, Phytophthora omnivora’, Tuburcinia Trientalis*, Proto- myces macrosporus *, the entrance of the germ-tube of the parasite into the cells of the host is more narrowly localised within the limits assigned above. While most perforating endophytes make their way into the interior of the cells of the host at any spot on their outer surface, the three Fungi above named make their entrance at the outer edge of the side wall which divides two epidermal cells, and then grow on in the middle lamella of this wall, splitting it in two and so pressing transversely or obliquely through the epidermis; ultimately they produce both an intracellular and an intercellular mycelium. ‘This is at least the prevailing mode of penetration in these species; perforation of the outer wall and lumen of an epidermal cell occurs exceptionally in Phytophthora. In some of the purely epiphytic Fungi which do not penetrate into the host, some for example of the Chytridieae* and the Laboulbenieae, the spores when conveyed by some method of dissemination adhere simply to the surface of the host, which is large in comparison to the parasite. The Lichen-fungi which live on small and usually unicellular Algae put out germ-tubes which embrace the cells of the host, as will be described in section CXV, when they encounter them in their elongation. It has never been observed that the direction of this growth is influenced by the host before contact. Kihlman ° has recently observed a very remarkable arrangement for fastening on the host in the case of Melanospora parasitica, which is epiphytic on species of Isaria. The almost cylindrical brown-walled spore, which is 5-6 p» in length, germinates by the emission of a germ-tube at each extremity, the tubes, whether grown in water or in nutrient solutions, being scarcely longer than the transverse diameter of the spore. If the spore lies against or on a hypha of Isaria, which is most frequently the case in a state of nature, the germ-tube becomes firmly attached to the hypha of the host and then developes into a mycelium. If the germ-tube comes into contact with an older hypha of Melanospora, the membrane which separates them is dissolved and they coalesce with one another. But if a germinating spore lies at some distance from a growing hypha of Isaria, and it is not difficult to procure this in plants grown on a microscopic slide, the direction of its growth in length is deflected towards the spore till it comes in contact with the germ-tube; which then unites with it and begins to develope. The greatest distance at which the germinating spore can influence the direction of growth of the hypha is from four to five times the length of the spore. The physiological analysis and explanation of all these phenomena of aggression, adhesion, and penetration through openings and membranes has yet to be undertaken. We can here only notice briefly some of the chief points to be considered. The facts which have been stated above with regard to the perforation show, on the one hand, distinct effects produced by the germ of the parasite on the host. The ' R, Hartig, Arbeiten d. forstbot. Instit. Miinchen, I, _ * Woronin, as cited on page 185. * Wolff in Bot. Ztg. 1874. * See above, p. 171. ® As cited on page 262. 366 DIVISION I1I.—MODE OF LIFE OF THE FUNGI. germ-tube causes a solution of continuity in the membrane which is being perforated in the line of the perforation. Where the perforation is a hole which is permanently fitted by the tube, as for instance in the chitinous skin of insects and in many plant-cell-membranes, it is natural to suppose that the hole is caused by partial dissolution of the membrane, and that this dissolution is the result of a fermentation which proceeds from the Fungus (see page 355). The case is somewhat different where, as in the perforating germs of Uredineae and Synchytrieae, the holes soon close up again. Here it may at least be asked, whether the perforating process from the tube or spore aéfached to the epidermis of the host does not split the membrane by purely mechanical means, much in the same way as a sharp needle divides the plate of cdoutchouc which is pierced by it, and whether the small split does not close up again purely in consequence of the elasticity of the membrane, as is the case in the plate of caoutchouc after the needle is withdrawn, when the turgescence in the perforating process sinks to nothing in consequence of the growth of the germ-tube, The deflection of Isaria by Melanospora can only be explained by assuming that some substance is secreted by the germinating spore which exercises a specific attraction on the growing hyphae of Isaria. On the other hand, the effects produced by the host on the parasite which is germinating or about to germinate are more varied than those of the parasite on its host, and a greater number of physiological questions are connected with them. We do not know the cause why germ-tubes penetrate through stomata, why some spores attach themselves to stomata, others to the surfaces of membranes, why the hyphae of the Lichen-fungi clasp the cells of the Algae in their embrace, and so on. We may make an attempt to explain the fact that certain parasitic germ-tubes perforate the epidermis of one species of Phanerogams and not of others by assuming the secretion of specific ferments and specific differences in the structure, firmness or cuticularisa- tion of the membranes of the host; but it is scarcely possible to explain from the data before us why a germ-tube bends its extremity towards the membrane of the proper host and not towards every membrane or moist surface, or even turns only towards the outer edges of the lateral walls of the epidermal cells, as in the cases mentioned above. Are specific physical irritations brought into play in these cases, or chemical stimulations,- which may be supposed to operate through unknown secretions from the surface of the host, with certain specific reactions on the part of the parasite? Questions of this kind present themselves here at every turn, as they do in some similar phenomena which se 2 in the saprophytes, and offer. very promising subjects for experimental enquiry’. Section CIII. The parasite pursues its further development as soon as it has attached itself to the host, while the living host reacts on the plant which occupies it permanently and sometimes continues to spread through it; this reaction varies extremely in different cases, being everywhere determined by the specific qualities of the symbionts. The chief phenomena attending these processes will be briefly + Pfeffer’s work on chemical stimuli, which appeared some time after the above words were written, has shown more distinctly the way to the answering of these questions, and has made some advance upon it. See Ber. d. Deutschen Botan. Ges. 1883, and Unters. d. Bot. Instit. zu Tiibingen, I, Heft 3 (1884). CHAPTER VII.—PHENOMENA OF VEGETATION.—PARASITES, 367 described in the following paragraphs and will be illustrated by examples. Some of them have been already noticed in passing in the sections of Chapter V, where they will be readily found with the help of the index. Further details must Be sought in the different monographs and in pathological treatises. Among the phenomena which are of quite general occurrence it may be mentioned in connection with the growth of the parasite, that in extreme cases it either continues to be confined to the spot where it first attacked its host and to its immediate neighbourhood, or spreads far beyond that spot; in the latter case it may grow through or over the existing parts of the host for considerable dis- tances, or part passu with the growth of the host, as is specially seen in many Lichen-fungi. In smaller hosts consisting of one or few cells, with the exception of the Lichen-fungi which will be described at length in the sequel, the difference between these cases is of course small; in larger plants on the contrary it is very striking. The Laboulbenieae, for instance, which are parasites on insects are narrowly confined to the part which they first attack ; the species of Cordyceps which belong to the Entomophthoreae grow through the entire body of the insect. Many corresponding examples might be mentioned from parasites on plants, and it need scarcely be added that there is no want of intermediate forms between the two extremes. Parasites which spread through the whole of the host, or over large portions of it it, may either show the same behaviour and the same development on every or almost every part of the body, or they may have certain phases of their development confined to certain parts, and this latter rule may be invariable or be very generally observed. Parasites on insects, species of Cordyceps for example, spread almost through the entire body of the creature; C. militaris puts forth its stromata at any part without distinction of the surface of the caterpillar which it attacks, often at many places at the same time; C. sphecocephala only on the under surface of the thorax between the first or between the two first pairs of feet of the West Indian wasp (Polistes Americanus) which is its host’. The same rule will be exemplified below in the case of very many parasites on plants, and has been already noticed to some extent in Chapter V. According to their effect on the host and the reactions of the host on this effect, two chief classes of parasitic Fungi may be distinguished, namely, a des/ructive and a /ransforming or deforming class; the two extremes are united by a large number of intermediate forms. When a parasite of the destructive class attacks and occupies its host the parts attacked by it become sickly, die, and are decomposed in a longer or shorter time without previously showing any signs of abnormal growth. It depends on the particular species whether these phenomena in large plants are confined to the parts directly attacked by the parasite or whether the whole body of the host becomes sickly and dies. All facultative parasites may be placed in this class, as will be shown in detail below; of obligate parasites on plant-forms the species of Phytophthora almost without exception, many Uredineae, such for example as the species of Puccinia which live on the Gramineae, or at least those portions of their life-cycle which inhabit the grass, and with some exceptions the Ustilagineae (species of Tilletia, Ustilago 1 See Tulasne, Carpol. ITT. 368 DIVISION III.—MODE OF LIFE OF THE FUNGI, Carbo, Claviceps, and many others) belong to the same category, together with all those that live on animals, unless we choose to reckon the phenomena of inflammation, suppuration, and formation of tumours caused by the presence of the Fungus in warm-blooded animals as cases of abnormal growth, a point which may for the present remain undecided. The occupation by the deforming parasite is followed immediately by anomalous processes of growth in the host or in the parts of the host, the word anomalous being here understood to mean every condition different from that which is found in the plants or the parts not attacked by the Fungus. Countless examples of this class of parasites are to be found among those which live on plants. The phenomenon necessarily presupposes a power of growth in the parts to be deformed, and in the higher plants therefore it usually implies that they were attacked in the young state when their growth is still incomplete. The extremes of deformation, which pass, it is true, readily into one another, consist on the one hand inan abnormal increase of growth and abnormal enlargement of parts of the tissue, which are in other respects normal and normally disposed, and hence in the swelling of the individual cells, as in the case of epidermal cells which are occupied by Synchytrium and the adjoining cells, or else in a monstrous enlargement and inflation of entire members and aggregates of members in the higher plants, such as the swelling of the flower-stalks and the enlargement, often to an enormous size, of the flowers of the Cruciferae when attacked by Cystopus. These may be said to be cases of hypertrophy. On the other hand the parts may be deformed with very slight or with no hypertrophy worth mentioning; such are well-known deformations of the shoots of herbaceous species of Euphorbia by Uromyces Pisi, U. scutellatus, and Endophyllium Euphorbiae, and the ‘witches’ brooms’ on the branches of the fir and cherry-tree when attacked by Peridermium elatinum or Exoascus. In the fir (Abies pectinata), for example, these branches grow vertically upwards, like small trees, from the horizontal limbs, with branches spreading in every direction, and leaves which spread in the same manner and fall off year by year, while the entire excrescence continues to grow for years’. In the flowers of Knautia arvensis, when occupied by Peronospora violacea, the stamens often, though not always, acquire the characters of normal petals of a beautiful violet colour, and the blooms are filled by them. These phenomena of deformation by Fungi may be termed mycetogenettc metamorphosts. The processes in the formation of Lichens, to which we shall recur in a later page, have a considerable resemblance to them. Lastly, the new formation of members, such as are not seen in any form on the plant when free from the Fungus, are caused on parts of some of the higher plants by the presence of the Fungus. The most striking instances of the kind are the delicate round bodies of the size of a cherry which Exobasidium Vaccinii produces on the leaves of the alpine rose, and the excrescences on the stem of Laurus canariensis, L. caused by Exobasidium Lauri and described at length by Geyler ?\—club-shaped for- mations. with blunt edges, of the length of a finger, and branched like an antler, which Schacht even mistook for aerial roots. But the strangest example of the kind is found in the Saprolegnieae when attacked by Rozella, which will be described below. Bot. Ztg. 1867, p. 257. * Bot. Ztg. 1874, p. 321. CHAPTER VII,—PHENOMENA OF VEGETATION.—PARASITES. 369 Excrescences of the kind just described and local hypertrophies caused by Fungi have been fitly compared with ga//s and have sometimes received that name. It is obvious that all these mycetogenous deformations and new formations and the phenomena also of simple destruction are in direct causal connection with the process of feeding the Fungus. In the latter case we see directly that the Fungus grows at the expense of the parts which are destroyed, the substance of its own body constantly increasing. In the case of tumours and hypertrophies there is often at first a striking over-production of building material, as starch, and this is afterwards used for the com- pletion of the development of the Fungus. In connection with this it often happens that the parts deformed by the Fungus are also killed prematurely; they die and are decomposed sooner than the same parts when free from the Fungus and not deformed. But every conceivable gradation is found in this respect in different species and some- times in different individuals between the parasitism which quickly destroys its victim and that in which parasite and host mutually and permanently further and support one another,—the relation which is most conspicuous in the formation of Lichens and which Van Beneden ? has termed mufualism. The phenomena here touched upon have not been submitted in any case to a strict physiological analysis ; but the general nature of the enquiry is so obvious that it is unnecessary to discuss it here. In the following summary of the chief phenomena and combinations which actually occur we must keep the Fungi which live on animals distinct from those which inhabit plants. FUNGI WHICH ARE PARASITIC ON ANIMALS. Section CIV. The Fungi which attack the bodies of living animals furnish a series of instructive examples of the phenomenon of facultative parasitism (see page 356). A number of species of Eurotium and Aspergillus (Sterigmatocystis), which all occur chiefly as saprophytes and in that mode of life reach their full development, in some cases even forming sporocarps, are able to migrate to the bodies of warm- blooded animals and live at their expense, producing an abundance of typical gonidia, but not, as far as we know, arriving at the formation of sporocarps. _ Their vegetation causes or promotes a diseased state of the parts, known to physicians as mycoszs, Aspergillus flavus, A. niger and A. fumigatus, Eurotium repens and Aspergillus glaucus are characteristic promoters of the disease of the human ear which bears the name of ofomycosts aspergillina®. The Fungi find a nidus in the diseased (serous) or excessive normal secretions of the skin, and their rapid growth causes inflammation and excoriation of the parts. But in these cases, as Siebenmann urges, they do not penetrate through the epidermis and are not developed in the healthy ear, so that they virtually retain their saprophytic character, however decidedly they must be considered to be promoters of disease. 1 Animal Parasites and Messmates (Internat. Scientific Ser. xix), See also De Bary, Die Erscheinung d. Symbiose, Strasburg, 1879. 2 Siebenmann, Die Fadenpilze Aspergillus, &c. u. ihre Beziehungen z. d. Otomycosis aspergillina, Wiesbaden, 1883 ; many special treatises on the subject are enumerated in this publication. [4] Bb 370 DIVISION III.—MODE OF LIFE OF THE FUNGI. Aspergilli of this kind, one of which has been certainly determined as Asper- gillus fumigatus, have been found since 1815, and especially since Virchow’s more recent and more exact account of them, spontaneously developed in the human lungs and in the air-passages of birds. ‘They find their way there no doubt, as they reach the ear, with the dust which mingles with the atmospheric air, and meet with similar conditions and adopt a similar mode of development. Gaffky and others, Lichtheim especially, obtained characteristic phenomena of development, in this case phenomena of disease, when the gonidia of Aspergillus fumigatus and A. flavescens, _Eidam, two species distinguished by the high optimum of their vegetative temperature, over 37° C., were introduced by injection into the blood of animals, such as rabbits and dogs. On the other hand, Eurotium Aspergillus glaucus, E. repens, Aspergillus niger, and Penicillium glaucum, the latter of which was once unjustly suspected by Grawitz, were proved by similar experiments to be incapable of development in animal bodies, and therefore harmless. Lichtheim found that the facultative parasitism of the two species of Mucor noticed above on page 359 was perfectly analogous with that of the two species of Aspergillus just mentioned, with the limitation only which was also noticed before, that Mucor rhizopodiformis has no endophytic development in the dog. The spores of these Fungi introduced by injection into the blood-passages are carried through them into all parts of the body. It would appear that they do not germinate in the blood-current itself, but in certain organs of the animal into which they are conveyed by the blood. The living organs show different degrees of liability to the attack of the Fungus, especially when the spores are injected in smaller quantities, and Lichtheim arranges them in the following descending series for the Mucoreae: kidneys, Peyer’s patches, mesenteric glands, spleen, marrow, liver. Similar results appeared with Aspergillus fumigatus, but with less regularity and with a characteristic localisation of the Fungus in the membranous labyrinth. ‘The living brain remained free in all cases from the development of the Fungus. But when the organs are dead the germination and development of the Fungi takes place in all in the same degree. The spores develope mycelia in living bodies, but it is only in exceptional cases that a fresh formation of spores takes place. The development of the Fungi is attended by characteristic local derangements, and these produce dis- turbance of the general health, for a fuller account of which the reader is referred to medical works* and especially to Lichtheim. Spontaneous Aspergillus-mycosis and Mucor-mycosis in internal organs re- moved from direct access of air is to say the least a doubtful occurrence. Many Fungi living in insects are obligate parasites. Everything of im- portance that is known of the development of the epiphytic Laboulbenieae which belong to this category has been stated at page 263. ‘Their dissemination by means of the spores conveyed from one insect which has been attacked by the Fungus to another, especially during the act of conjugation, has been clearly described 1 See especially Virchow, Archiv, IX (1856), p. 557,—Fresenius, Beitr. p. 84,—Lichtheim, in Berliner klinische Wochenschrift, 1882, Nr. 9 and in Zeitschr. f. klin, Med. VII, Hft. 2.—Gaffky, Mittheil. aus d. k. Reichsgesundheitsamt, I, 526. These papers contain further notices of the literature of the subject. | q CHAPTER VII.— PHENOMENA OF VEGETATION.—PARASITES, 371 by Peyritsch? in the case of the house-fly. The health of the insect attacked by these epiphytes seems to be very little disturbed. The development of the Entomophthoreae which attack insects has also been given above (page 158). We may add here that the body of the insect is occupied in essentially the same way as by the species of Cordyceps which will be described below. The Entomophthoreae, like the Laboulbenieae, are, as far as is known, strictly obligate parasites, and go through the whole course of their development, with the exception only of a brief stage of germination, in and on their host while it is either still alive or recently killed by their vegetation. The life-history of the species of Cordyceps which attack insects is more complicated. Cordyceps militaris, as examined in caterpillars, may be taken £ FIG. 165. Cordyceps militaris, Fr. A secondary spores from the asci germinating in water on a microscopic slide. @ a single spore with one of its germ-tubes erect and branched, its extremity and the branches having formed chains of gonidia. 4 three secondary spores germinating ; the germ-tube of one of them has risen into the air and formed a chain of gonidia on its apex. 2B extremities of hyphae which have penetrated through the chitinous skin of a caterpillar, have reached its inner surface and are abjointing cylindrical gonidia. C cylindrical gonidia with sprouts, from the blood of a caterpillar attacked by the Fungus; one extremity of d is fixed in a blood-cell. Z£ extremity of a filiform gonidiophore which has grown out of the skin ofa caterpillar of Sphinx Euphorbiae killed by the Fungus and converted into a sclerotium, Magn. about 400 times. as an example*, The ascospores formed in the orange-coloured club-shaped stromata are ejected as narrowly filiform or rod-shaped bodies divided by transverse walls before they leave the ascus into a row of many shortly cylindrical secondary. spores, which are at least 160 in number, When placed in any fluid, they usually. separate from one another, swell slightly, become rounded in shape and then put out germ-tubes (Fig. 165, 4); sometimes, but not always, the spores become partially united together again by means of short connecting tubes before they germinate.. Germination takes place on the surface of the skin of a caterpillar if it is only slightly moist. The germ-tubes penetrate at once, and at any part of the surface, into the chitinous skin of the insect. Here they enlarge into somewhat stouter fungal hyphae, which ramify and in the simplest case make their way by a sinuous course into the deeper layers of the skin, at length reaching the inner surface and insinuating them- selves between the bundles of muscles and lobes of fatty substance of the creature, 1 As cited on page 273. * Bot. Ztg. 1867, p. 1, and 1869, p. 59go. B b 2 372 DIVISION III.—MODE OF LIFE OF THE FUNGI. Here their further growth in length ceases; but now begins, sometimes even within the soft inner layers of the skin itself, the successive abjunction apparently in small quantities of longish cylindrical gonidia, known from their shape as cylinder-gonidia, partly on the extremities of the primary branches, partly on short lateral branchlets (Fig 165 2). From the place of their formation these pass at once into the blood which fills the cavity of the body, where they elongate to twice or several times their original size, and divide repeatedly by transverse walls, and then begin to develope like Sprouting fungi, i.e. they produce repeated orders of similiar cells by terminal and lateral sprouting (Fig. 165 C). These cells are disseminated through the blood by the movements of the insect and fill it by degrees in a dense mass. They also penetrate into the blood-ceils or are embraced by them in the course of the amoeboid movement of the latter (Fig. 165 C, d). They grow at the expense of the blood, which diminishes in quantity to such a degree that the insect at length loses its normal turgidity, becomes soft and relaxed and in this state dies. As soon as death has taken place all the sprout-cells begin to develope rapidly at the expense of the substance of the dead body into copiously branching hyphae, which not only fill the entire cavity of the body which till now contained the blood with a dense weft and expand it to its former size in the turgescent state, but grow in a dense mass through all parts of the body, except the intestinal canal which remains empty, and to a great extent absorbs them. A body is thus formed in 1-2 days’ time which retains the shape of the living insect, but consists of a close weft of fungal hyphae with some small remains of the body of the insect. This Fungus-body with the form of an animal has the biological peculiarities of a sclerotium. It can give rise directly to fresh stromata, and can do this in a few weeks after its formation if it lies in a moist state; if it is dried, it passes into a resting-state the maximum duration of which is not exactly determined, but it may certainly continue for some months without pre- judice to the power of further development. Such is the course of development of Cordyceps in its simplest form. But deviations from this course and complications of it occur not unfrequently, of which the following are the most important. If its ascospores are sown in water or in nutrient solutions without a living host, they germinate and the germ-tubes develope hyphae which branch with more or less copiousness according to thé amount of nourishment supplied ; in water only small-plants are produced with few or no branches (Fig. 165 A, a, 4). Some of the branches spread as a mycelium in the nutrient solution, and have the power, like the hyphae on the inner surface of the cater- pillar’s skin, of abjointing cylinder-gonidia. It is true that this has not been observed in the species in question, but it may be safely assumed since it has been observed in Botrytis Bassiana, which agrees with Cordyceps in all these biological relationships. Other branches of the germ-plants rise erect from the fluid into the air and branch, forming whorls of ramifications on the extremities of which they serially and successively abjoint gonidia (see p. 66). The first gonidia on the young germ-plants are cylindrical like those in the body of the insect (Fig. 165 A, 4), only usually shorter. All the succeeding ones, even the second in arow which began with a cylindrical gonidium, are spherical in form; they may therefore be called round or aerial gonidia. The mycelium also which is developed in the dead body of the caterpillar very often produces gonidia of this kind only and no cylindrical ones, CHAPTER VII,—PHENOMENA OF VEGETATION,—PARASITES. 373 The gonidiophores of these plants on most of the caterpillar-bodies examined, which also bore stromata, were observed to be small hyphal branches with whorls of branchlets like the germ-plants just described (Fig. 165 4), and these together formed a delicate down on the surface. But on other insects they grow into a dense mould-like covering some millimetres in height and white with a dust of countless gonidia, or else like the Coremium-form of Penicillium they form club- shaped Fungus-bodies 1-2 centimetres in height and covered all over or in the upper part, which is borne on an orange-yellow stalk, with a felt of branchlets which abjoint gonidia. The last-named bodies are known as form-species under the name of Isaria farinosa. Both the Isaria-form and mould-covering are found commonly on a sclerotioid insect-body by themselves, i. e. without the stromata. I once succeeded in obtaining two poorly developed stromata with some large Isarieae from a caterpillar of Spinx Euphorbiae infected by ascospores, which had changed to the chrysalis state after infection. Gonidiophores with the round aerial gonidia are also obtained if cylinder-gonidia from the still living insect or portions of the mycelium from the insect converted into a sclerotium are cultivated in the air on a suitable substratum; the amount of luxuriance with which they are developed varies with the supply of food. They are formed too under the same circumstances on small plants, which proceed from germ- tubes produced at once in a fluid from the aerial gonidia themselves. ‘These germ- tubes do not ultimately penetrate into the skin of the insect, at least not in the experiments made with the caterpillar of Sphinx Euphorbiae. When the insects are sprinkled with the spores the germ-tubes are seen to enter the tracheae through the stigmata, and then to bore through the wall of the tracheae and so reach the cavity of the body, where the cylinder-gonidia are then abjointed and disseminated, and sprout; at length the insect dies and becomes a sclerotium, exactly in the way described above in the case of the direct products of the ascospores. Stromata have never been known to be formed on insects killed by infection with aerial gonidia, only a fresh crop of aerial gonidia especially of the Isaria-form. The Fungus therefore which we are describing can only arrive at its full develop- ment, that is, can only form perithecia, as an obligate parasite, and to this mode of life it is closely adapted. When it ceases to be a parasite and the dead insect becomes a sclerotium, we see a saprophytic stage of the existence of the plant follow upon the strictly parasitic stage. When the conditions for a parasitic mode of life are withdrawn, facultative saprophytism takes its place (see page 356), and a new form of adaptation may make its appearance with the formation of aerial gonidia accom- panied also with the normal formation of perithecia. The entrance upon the parasitic mode of life is however comparatively easy, because the formation of all kinds of spores takes place abundantly in nature, especially in wooded places frequented by the insect-hosts. All that is known of the mode of life of other insect-killing Fungi allied to Cordyceps militaris agrees entirely with the account here given of that species. The foregoing account of the life-history of Cordyceps is founded chiefly on the facts observed on infecting the caterpillars of Sphinx Euphorbiae with the Fungus, and on investigations some of which have not hitherto been published. I make this latter remark, because the statements agree so exactly with the account given by 374 DIVISION III.— MODE OF LIFE OF THE FUNGI. myself! and supplementing that of Vittadini? of Botrytis Bassii, the Fungus of the ‘muscardine’ of the silk-worm caterpillar which was formerly only known to produce gonidia, that it might be thought that I had simply transferred the observations on the one species to the other. The truth is that the two agree perfectly with one another. Slight deviations from the course described in one species of insect occur in the case of other species both in the reaction of the insect on the effects produced by the parasite as well as in the development of the latter, as I have shown in another place in connection with Botrytis Bassiana. A case of such deviation may be mentioned here as occurring in Cordyceps. The caterpillars of Sphinx Euphorbiae when infected with the ascospores were killed in from fifteen to twenty days, and the spots in the skin infected by the Fungus showed, as in Botrytis Bassii, nothing beyond a brown discolo- ration varying with the individual and spreading all round from the intruded hyphae. The process was somewhat different when the caterpillars of Gastropacha Rubi were infected. First of all it was much slower; of seventeen specimens infected the first died in about thirty days, the last not till after the lapse of seventy days, and death was preceded by slowly increasing weakness. In the second place the skin showed signs of disease in the spots where the spores had been sown after the Fungus had penetrated into the live insect, but long before its death; it swelled up and became of a darker colour and hard, and was covered with a delicate white mould composed partly of the regular verticillately branched gonidiophores of the species, partly of accumulations of small roundish colourless cells and shortly cylindrical pieces of hyphae divided by a few transverse walls. These hyphae not unfrequently abjointed normal gonidia on narrowly conical lateral branchlets. It could not be determined whether these structures were produced by the breaking up of mycelial hyphae or by the development of normal gonidia. They showed themselves to belong to Cordyceps by the fact that they all gave rise to mycelia with characteristic verticillately branched gonidiophores when cultivated on microscopic slides. The above statements respecting the entrance of the Isaria farinosa-form into the host are reproduced from my paper in the Botanische Zeitung for 1869, which should be consulted for further details. In this paper and in that of 1867 I gave expression to some doubts with respect to the view maintained by Tulasne’, that Isaria farinosa belonged to the cycle of development of Cordyceps militaris ; these doubts were sug- gested partly by the failure of attempts to obtain stromata and Isaria-forms in turn from one another in specimens under cultivation, partly by differences, which it is true were only quantitative, in the ramification of the branches producing gonidia. The latter objection might easily be dismissed, and as has already been remarked in the text I do not now think it necessary to maintain the first. A caterpillar of Sphinx Euphorbiae, which had become a sclerotium as usual after infection by ascospores, when laid on moist sand produced first of all two small stromata provided with normal perithecia, These died before the asci were fully formed, and then Isaria was produced in abundance. Portions of mycelium cultivated on microscopic slides had already afforded Isaria. In this case therefore either Isaria was uitimately produced from the ascospores, or the insect had been infected with them and unintentionally also with Isaria, which in the end stifled and supplanted the form with perithecia. I have no reason for assuming such accidental mingling of the two forms, and have framed my opinion accordingly ; at the same time the possibility of the mixture is not excluded and it was necessary to call attention to that fact. For some further remarks on Cordyceps, Botrytis Bassii and some other forms see above, page 253. 1 Bot. Ztg. 1867. ? Della natura del Calcino o mal del segno (Giorn. Instit. Lombard. III (1852), p. 142, c. t. 2) * Carpol. III. CHAPTER VII.—PHENOMENA OF VEGETATION.—PARASITES. 375 Section CV. Our knowledge of the Fungi which are parasitic on animals, other than those contained in the groups which have now been considered, is so small from the botanical point of view, that, with all due acknowledgment of the medical interest of these plants and medical research, we can only touch upon them briefly in this place. In doing this we shall refer especially to the medical works on the subject and to important special treatises, from which the reader will obtain further directions if he wishes to examine the somewhat profuse literature in greater detail’. We cannot of course enter here into purely medical questions. The most important of the plants in question are the parasitic Saproleg- nieae, the Fungi which cause diseases of the skin in warm-blooded animals, men included, the Fungus of thrush or aphthae, and Actinomyces. Some kinds comprised in this class are quite doubtful. Parasitic Saprolegnieae. Numerous cases are recorded in which living fish, such as gold-fish, and other creatures living in water, as salamanders and frogs, were attacked by Saprolegnieae, grew sick and died®. Destructive epidemics among salmon have recently been reported, especially in the English and Scottish rivers, and these epidemics are characterised by the development of Saprolegnieae*. We learn - from Huxley’s investigations that the Fungus settles on portions of the skin of an apparently healthy fish where there are no scales and sends mycelial or rhizoid- branches through the epidermis into the inner layers of the skin, causing at first local and then general disturbance of the system. Similar statements are made in other cases. The examination of the Fungus has only shown that it is some form of Saprolegnia. The formation of oospores, on which the determination of the species depends, was either not observed or imperfectly described. Disregarding Huxley’s results for the moment, we may gather from the statements before us that the Fungi in question are ordinary Saprolegnieae, which must have migrated to the living animal as facultative parasites, since they usually vegetate as saprophytes (see page 141). If this is so, there must have been some peculiarity in the fishes before they were attacked by the Fungus, which is not found in the same fishes in the natural state; there must be some special reason for their being attacked by the Saprolegnia, perhaps a disease of some other kind which we must not enquire further into here; for the ordinary species of Saprolegnia are so abundant in our streams and lakes, that if they could attack the fish indiscriminately as facultative parasites, not one could possibly be free from the Fungus. Direct experiments also have shown me that healthy gold- fish may continue lively and free from the Fungus for months in water, in which Saprolegnieae kept purposely in large quantities were forming an abundance } The material collected from time to time will be found in the following publications :— Ch. Robin, Hist. nat. d. végétaux parasites qui croissent sur Fhomme et les animaux vivants, Paris, 1858. Kuchenmeister, Die an u. in d. Kérper d. Menschen vork. Parasiten, II, Leipzig, 1855. Steudener in Volkmann’s Samml. klinischer Vortrage, Nr. 38, Leipzig 1872. Baumgarten, Pathogene Mikroorganismen, I. (Deutsche Medic. Zeitung, 1884, 1). ? Hoffmann in Bot. Ztg. 1868, p. 345, and the older works on the Saprolegnieae noticed above on page 145. * Huxley in Nature, Vol. XXV (1881-1882), p. 437. See also the English he hice in Just’s Jahresber. V, 96, 456, IX, 253. 376 DIVISION IlI.—MODE OF LIFE OF THE FUNGI. of spores. It would of course alter the case if there were distinct parasitic species of Saprolegnia different from the common ones, but we know of no such species at present. The remarks here made apply on the whole to the epidemic among salmon investigated by Huxley, but some points require further explanation. The Fungi in this case appear on the outer surface of the skin in the form of ordinary Saprolegnieae ; they could be transferred by tapping to dead flies and be made to develope further on them, but their gonidia are described as being always without motion. This at once raises the question whether they really belong to Saprolegnia, and at any rate it is quite uncertain whether we are dealing with a case of facultative parasitism in species which are usually saprophytic or with one or several peculiar and specifically parasitic forms. - Section CVI. The following are the best-known species of Fungi of diseases of the skin. Achorion Schoenleinii, Remak, the Fungus of favus, Trichophyton tonsurans, Malmsten, the Fungus of ringworm or tinea (herpes) tonsurans which is identical according to Kébner with that of sycosis or mentagra parasitica (Microsporon Audouini and M. Mentagrophytes, Rob.; Microsporon furfur, Rob., the Fungus of pityriasis versicolor’). These Fungi are parasitic on the skin of different mammals and birds. They grow luxuriantly in and beneath the epidermis, in the hair-follicles and hairs. Their appearance on the human skin is characterised by the forms of disease enumerated above. Trichophyton tonsurans has also been observed on horned cattle, horses, dogs, and rabbits, Achorion on the domestic mouse, the rabbit and the head of domestic fowls; Microsporon furfur was seen by Kébner on rabbits after inoculation. They may all be conveyed from one individual to another, from men to other animals and vce versa by sowing their spores, and as these develope, the characteristic disease in each case makes its appearance. Transference by inoculation can be successfully performed on sound individuals, but certain forms of predisposition in the patient, which we cannot discuss here, appear to favour or to hinder the development of the Fungus. Of these Fungi as they appear in and on the portions of the skin attacked by them we know only the septate mycelial hyphae, the branches of which divide trans- versely into rows or chains of spores capable of germination and resembling those of Oidium lactis or the chain-gemmae of Mucor (see pages 67 and 155). When 1 Remak, Diagnost. u. Pathogen. Unters. Berlin (1845), p. 193. Kébner, Ueber Sycosis, &c. in Virchow’s Arch., XXII (1861), p. 372 ;—Id., Klinische u. experi- mentelle Mittheil. aus d. Dermatologie u. Syphilidologie, Erlangen, 1864. — Strube, Exanthemata phyto-parasitica eodemne fungo efficiantur (Diss. inaugur. Berolini, 1863). J. Lowe, On the identity of Achorion Schénleinii and other veg. parasites with Aspergillus glaucus (Ann. mag. nat. history, ser. 2, XX (1857), p. 152). W, Tilbury Fox, Skin diseases of parasitic origin, London, 1863. Kleinhans, Die parasitéren Hautaffectionen, Erlangen, 1864. P. J. Pick, Unters. ii. d. pflanzlichen Hautparasiten (Verhandl. d. Zoolog-Bot. Ges. in Wien, XV, 1865). J. Peyritsch, Beitr. z. Kenntn. d. Favus (Medicin. Jahrb. Bd, XVII, Wien (1869), Heft II, p. 61). P. Grawitz in Virchow’s Archiv, 70, p. 546. Ed. Lang, Vers. einer Beurth. d. Schuppenflechte (Vierteljahrschrift f. Dermatologie u. Syphilis, 1878, p. 333) ;—Id., Vorlauf Mittheil. ii. psoriasis (Ber. d. naturw. Med. Vereins z. Innsbruck, VIII, 1878). CHAPTER VII.—PHENOMENA OF VEGET'ATION.—PARASITES. 377 fresh spores also are sown in nutrient solutions the germ tubes which are at once emitted develope only mycelia producing spores in the manner just described. In this respect, according to Grawitz, Achorion, Trichophyton, and Microsporon are exactly alike, but they differ from one another in size. This difference is attributed by Grawitz to differences in the food, which can no doubt give rise to great diversity of size in the same species, and he therefore considers the three forms as belonging to one and the same species; and he further identifies this species with Oidium lactis, partly on the ground of the resemblance of the three forms when grown in a nutrient solution to Oidium, and partly because inoculation with pure Oidium will produce diseases of the skin which resemble a mild herpes. The view that these four forms belong to one another cannot on our part be summarily rejected, but at the same time it requires further proof. In any case the comparison with the Mucor which forms gemmae shows that those forms do resemble imperfectly developed states of other known species of Fungi with typical gonidia and carpospores. Hence the question arises whether organs of this description: are to be found also in skin-parasites. On the answer that may be given to this question will depend the determination of the special qualities of these Fungi as parasites. At present the question is still unanswered, though many attempts have been made to solve it in past times by means of artificial cultivation ; but Saccharomyces, Penicillium, Eurotium and all sorts of Moulds made their appearance in the impure material used for these experiments, and then the skin-parasite was introduced in one way and another without reasonable ground into the cycle of forms of these species, as Peyritsch long since clearly showed. It has been proved by experiment that Saccharomyces albicans, Reess (Oidium albicans, Robin) causes a formation of pustules and scab, known as thrush or aphthae, on the mucous membrane of the mouth, throat, and oesophagus especially in young individuals. Grawitz and Reess' have recently shown that the plant is a form of Sprouting Fungus with long cells resembling Saccharomyces Mycoderma ; its ascospores have never been observed ; it does well as a saprophyte, but excites weak alcoholic fermentation in saccharine solutions and is therefore a facultative parasite. It has yet to be determined whether it is identical with S. Mycoderma (the flowers of wine) or with some similar form. Section CVII. The name of Actinomyces Bovis has been given by Harz to a remarkable growth discovered by Bollinger and Israel which occurs in peculiar swellings on the jaw-bone, especially in cattle, and is in causal connection with them, but is also found inside certain parts of the body in pigs and men”. In the swelling, 1 Grawitz in Virchow’s Arch. 70, p. 566, and 73, p. 147.—Reess, Ueber d. Soorpilz (Sitzgsber. d. Phys. Med. Ges, zu Erlangen, 9 Juli 1877 and 14 Jan. 1878). The literature of the subject is given by Kehrer, Der Soorpilz, Heidelbg. 1883. ? Bollinger, Ueber eine neue Pilzkrankheit beim Rinde (Centralbl. f. med. Wiss. 1877, Nr. 27). J. Israel, Neue Beob. v. Mycosen d. Menschen in Virchow’s Arch. 74 (1878), and 78. O. Harz, Actinomyces Bovis. (Deutsche Zeitschr. f. Thiermedicin, 1. Supplementheft (1878), p- 125). See also in the same publication, p. 45. E. Ponfick, Die Actinomycose d. Menschen, Berlin 1882. Johne, Die Actinomycose (Deutsche Zeitschr. f. Thiermedicin, VII, (1882), p. 141, tt. 8—ro), Pusch, Ueber Lungenactinomycose (Arch. f. wiss. u. pract. Thierheilkunde, IX (1883), p. 447). In this paper the different works on the subject are most fully enumerated. 378 DIVISION III.—MODE OF LIFE OF THE FUNGI..- which we must not describe at greater length in this place, Actinomyces forms yellow bodies like sand-grains about 1 mm. in diameter. The larger of these bodies, which are visible to the naked eye, always consist of a number of single growths of Actinomyces united into a mass by the soft swollen tissue. Each Actinomyces may be best described as a round or less commonly elongated hollow body sometimes pressed flat with a relatively thick wall and narrow cavity. The wall looks like a dense hymenomycetous or discomycetous hymenium with very slender elements, being composed of filaments which are copiously branched and have their branches at right angles to the surface and therefore radially disposed when the form of the body is round, and are crowded close together and difficult to separate from one another. Many of these crowded branches are club-shaped at their outer extremity, and in this point again therefore may be compared with asci or narrow hymenomycetous basidia ; some are constricted and torulose. They mostly end at a uniform height in the smooth outer surface of the body, though single ones some- times extend a long way beyond the rest according to the figures which are given (see Ponfick, t. vi). The inner cavity of the body, which is surrounded by this kind of wall and as was said is comparatively narrow, is filled with a dense tangled mass of slender much- branched filaments, the branches of which are continuous with those of the wall. Roundish or elongated grains of about the thickness of the filaments and not unlike small spores are found between the filaments, at least in some specimens. The filaments appear to be filled with a homogeneous protoplasm, in which single granules or perhaps vacuoles are rarely to be distinguished ; it is uncertain and a disputed point whether they are septate. They attain at most a breadth of 2-3 p in the broadest parts of the club-like swellings which I could find, in other parts scarcely a third of that measurement. The Actinomyces is sometimes incrusted with lime. The structure of Actinomyces certainly favours the view that it is of the nature of a Fungus, but it has no closer resemblance than this to well-known Fungi. It is not possible therefore to assign it a place in the system, or to form any clear idea of the history of its growth and development from the analogy of other Fungi. Experiments in its cultivation outside the body of the animal have yielded no results of importance to our knowledge of its development. All that can be said about it is founded entirely on the state of things observed in the creature attacked with actinomycosis either living or dead. From the experiments of Ponfick and especially of Johne it would seem possible that Actinomyces grows, because when fresh matter was introduced by inoculation beneath the skin or in hollow places in the bodies of horned cattle, the specific swellings containmg Actinomyces were produced in them even in parts of the body at a distance from the places where the inoculation was performed. That the latter were a new growth and not the individuals introduced by the inoculation is certainly not proved, but is not to be disputed; at any rate there can be no doubt that actinomycosis is produced by inoculating with Actinomyces. We can frame concep- tions of our own as to how growth is eventually brought about, but none of them rest on a secure foundation, The same writers found often in fresh material the club-shaped elements of the wall-layer separated from one another, and a large number of club-shaped sprouts CHAPTER VII.—PHENOMENA OF VEGETATION.—PARASITES. 379 shooting from them, especially from their basal portion, so that the whole was palmately lobed in form; these clubs, or also, as is stated, portions of them delimited by transverse divisions, may then be regarded as spores (‘ gonidia, conidia’), the sprouting or branching of which may give rise to a new plant. On the other hand we must not forget the round bodies which are sometimes found in the inner cavity and which may be spores, nor the occurrence of small plants which consist almost entirely of the slender filaments and the origin of which from the sprouting of the clubs is not fully explained. But all this still leaves us in entire ignorance of the real history of growth. The failure of the attempts which have been made to cultivate Actinomyces outside the body of an animal, supposing always that it is really a plant, leads naturally to the assumption that it is an obligate parasite. But even this may be doubtful. From the experience of the pathologists who relied chiefly on the local occurrence of the swellings, it is probable that the surface of the mouth and throat and in some cases small wounds on them are the parts where the presumed parasite makes its entry and attacks the animal, and that it is conveyed there with the food. Johne frequently found in the pockets of the tonsils of pigs, even when the animals were quite free from actinomycosis, small bits of plants rough with spikes, such as bits of the awns of grain and the like, and Fungus-bodies resembling growths of Actino- myces attached to them in considerable quantities. Further investigation is required to explain the true meaning of all these observations. A peculiar disease known as the madura disease, which is endemic in some districts of India and causes dangerous swellings and degeneration in the feet and hands, has been ascribed to a parasitic Fungus, named by Berkeley Chionyphe Carteri'. More thorough investigation has shown that it is at least doubtful whether there is any causal connection between the disease and the growth of a Fungus. Fungus-elements are found, but not invariably according to more recent accounts, in the swellings, and there is no ground whatever for supposing it to belong to the form obtained by cultivation on rice-pap which bears the name of Chionyphe. It is hard to say what this Chionyphe itself is. ; The often described occurrence of Fungi in eggs is a special case of saprophytic vegetation, and is not therefore one for consideration here. PARASITES ON PLanrTs. a. Facultative parasites. Section CVIII. Parasites on plants display much greater variety in their adaptations to their peculiar mode of life than those which live on animals. A quite gradual, passage from saprophytes to parasites is effected especially by the facultative parasitism of certain saprophytic Moulds which cause rottenness in orchard fruits; the softening of pears, it should be observed, is not due to the action of a Fungus. These phenomena were investigated by Davaine’ in 1866, and 1-H, J. Carter, in Ann. mag. nat. Hist. IX (1862), p. 442, and in Journ. Linn. Soc. VIII, 1865. M. J. Berkeley, in Journ. Linn. Soc. VIII, 1865. H. V. Carter, Mycetoma or the fungus disease of India, London 1874. Hirsch in Virchow’s and Hirsch’s Med. Jahresber. X, 1 (1875), p. 437, XI, 1 (1876), p. 382. Lewis and Cunningham, The Fungus Disease of India, Calcutta 1875. ? Recherches sur la pourriture des fruits (Comptes rend. 83, pp. 277, 344). 380 DIVISION III.—MODE OF LIFE OF THE FUNGI. afterwards by Brefeld'. Species of Mucor (M. stolonifer and M. racemosus), Penicillium glaucum, Trichothecium roseum, and other species are able to make their way into sound juicy fruits, and vegetate and cause rottenness in them. These do not rot without the Fungi. If spores are sown on the uninjured surface of thick-skinned fruits like the apple and pear, where there is sufficient moisture for germination, the germ-tubes are unable to penetrate into them or do so with difficulty; but they enter with ease if the spores are sprinkled on wounded places where the skin is broken. Mycelia which have already acquired some strength are better able to force their way through the unbroken skin. The softer the fruits have become from other causes the more easily are they penetrated by the Fungus ; fruits therefore like strawberries and raspberries with thin skins are” very liable to be attacked. Davaine found that the vegetative organs of succulent plants, such as Sempervivum, Mesembryanthemum, and Stapelia show the same phenomena as thick-skinned fruits. Observation of the fruits shows that the Fungi develope more easily the nearer the vital powers of the parts attacked are to their lower limit, and at this point the conditions of saprophytic vegetation make their appearance. The parasitic phase of vegetative life is seen in its more characteristic form in many other facultative parasites on plants, and with many shades of difference in different species. The Sclerotinieae, Pythieae, Nectrieae, and Hartig’s tree- destroying Hymenomycetes may be taken as examples for closer consideration. Many other Fungi, species of Pleospora and Cladosporium for example and allied forms will have to be added to this if the group is more thoroughly investigated. Of the Sclerotinieae, Sclerotinia Sclerotiorum (see pages 30, 52, 218) may go through the whole course of its development as a saprophyte and finds opportunity for this in the natural state on dead plants. But it can also attack certain living and healthy plants and parts of plants as a parasite and destroy them. But according to our present experience it always requires to go through a previous stage of existence as a saprohyte in order to be capable of parasitism. The allied S. ciborioides which preys on clover behaves in a similar manner. Sclerotinia Fuckeliana inclines more in the direction of saprophytism; both the mycelia which produce gonidia and those which form sclerotia are found chiefly in dead parts of plants, especially on decaying leaves, &c. At the same time it is one of the chief agents in the production of decay in juicy fruits, and more thorough investi- gation will confirm the experience drawn from every conservatory, that the mycelium when it has once reached a certain degree of strength becomes parasitic on living plants and kills them. I have previously? given a very imperfect account of the circumstances connected with the vegetation of Peziza Sclerotiorum, and at that time I also misunderstood to some extent the facts which were stated about it. More recent observations have given me a clearer understanding of the matter and it will be well to describe them here in greater detail. The ripe ascospores germinate in pure water, emitting short tubes which soon cease from further development ; ina suitable nutrient solution, in must of grapes for instance and onripe juicy berries of any kind, they develope into a vigorous mycelium which forms sclerotia, and the same result is obtained if they are sown on dead vegetable 1 Sitzgber. d. Naturf. Freunde zu Berlin, Dec. 21, 1875. See Bot. Ztg. 1876, p. 281. ? See the first Edition of this work, p. 215. CHAPTER VII.—PHENOMENA OF VEGETATION.—PARASITES. 38 I substances, and even according to Brefeld on bread. If the spores for example are sown on a piece of carrot which has been killed by hot water, a vigorous fungal growth is obtained ; but on the moist surface of living portions of the same plant only short germ-tubes are produced, as in simple water, and these do not penetrate into the living tissue, even where the surface has been injured; the parts which have been sown remain for weeks free from the Fungus. If on the contrary the infection of the sound part is due to germ-tubes which have developed to a small amount only in a nutrient solution—how much cannot be exactly stated, but it is sufficient if the germ tubes are scarcely visible to the naked eye,—they penetrate at once into the living tissue and kill it, and form mycelium and sclerotia; pieces of older mycelium behave in the same way. The results are obtained with all parts of the plant, according as they are alive or dead and are inoculated with spores or with germ-tubes which have reached a certain stage of development. I never saw a germ-tube make its way into living tissue without having been previously nourished as a saprophyte; some statements to the contrary will be noticed in the sequel. But Sclerotinia Sclerotiorum is also found as a parasite on living cultivated plants, not to mention the injury which it does to turnips in store. I observed it destroy the beans (varieties of Phaseolus vulgaris) in a garden in the neighbourhood of Bregenz two years successively, and a similar occurrence has been reported recently by Prillieux from Algeria’. It is also very fond of attacking Zinnia elegans and the Petunias. If we try to infect sound specimens of these favourite species, even quite young seedlings, with spores which are germinating in pure water, we always get the same negative result as in thé carrot; the plants remain uninjured. If an extremely small amount of some nutrient solution is supplied to the germ-tubes emitted by the spores they at once become strong enough to penetrate into the plants at any place and then to develope into a mycelium which will spread through them and destroy them and form sclerotia, unless the amount of food which it obtains is insufficient, as in the case of seedlings. The same results were obtained with older vigorous mycelia. In the case of plants growing naturally and rooted in the soil we can see how the Fungus as a rule makes its way into the stem from the surface of the ground, and leaving the roots untouched ascends in the tissue of the aerial parts, especially in the masses of parenchyma. In this way the whole plant is killed and dried up and becomes of a pale straw colour. During this process it is not necessary for the Fungus to appear on the surface ; in fact it often re- mains quite inside and then forms its sclerotia in the shape of cylindrical or prismatic bodies inside the dead pith especially in the neighbourhood of the nodes, or, as in Phaseolus, in the fruits also between the ovules ; in Zinnia it often fills the receptacle with a sclerotium which like it is conical in shape. In a very moist environment however the mycelium may come out to the surface of the plant which it has attacked in smaller or larger quantity in white flakes and tufts, and can also form its sclerotia there ; it may also pass over to the foliage of neighbouring plants with which it comes into contact, and destroy them, proceeding from above downwards. This may be observed in a very striking manner where beans stand close together in a plot. All these phenomena may easily be reproduced by artificial cultivation in pots. It is only necessary to place some mycelium, grown from spores and made capable of infec- tion in the way described above, at the base of the plant to be infected, and keep the whole sufficiently moist. Experiments have shown that commencements of mycelia capable of infecting other plants may be obtained from spores on a small bit of dead vegetable substance, a piece for instance of a dead leaf. The mycelia therefore may be formed on every bit of moist ground covered with vegetation to which the spores find their way. Sporocarps formed spontaneously from sclerotia of the previous year were to be found in the bean-garden just spoken of, and these supplied the spores. As a saprophyte the Fungus developes on all dead parts of plants employed in 1 Comptes rend. 99 (1882), p. 1368. 382 DIVISION III—MODE OF LIFE OF THE FUNGI, its cultivation, though they may supply unequal amounts of nutrient material. On the other hand it by no means attacks every kind of Phanerogam as a parasite. I was unable to find, after repeated and careful search, any trace of the Fungus on the plants of a moist meadow close to the beans above mentioned. Among plants under cultiva- - tion one variety of Phaseolus vulgaris in the same garden was very slightly infected with the Fungus in spite of the immediate proximity of the others. Experiments in inoculation also showed that Phaseolus multiflorus was scarcely ever attacked ; in other specimens the Fungus developed only scantily, but in single young seedlings kept very moist its growth was vigorous. Living plants of Brassica (B. rapa, B. Napus, and B. oleracea) were never attacked, either as young seedlings or as plants ready to blossom. Further details must be reserved for another place. It should be added, that the hyphae of the Fungus when once they have become capable of infecting make their way into the superficial living cells by piercing their walls, and grow indiscriminately in and between and through the cells of the living tissue and soon kill them. The power of infecting is shown by the power of penetrating the membranes, which are evidently dissolved at the points of penetration. Hence it is very probable that this power depends on the presence of a substance which can dissolve a membrane, a ferment in fact, and that this substance is not formed and discharged in sufficient quantity till the germ-tube from the spore is properly nourished and developed. The foregoing statements with regard to the power possessed by Sclerotinia Sclerotiorum of infecting are in opposition to some which have been published in other works and especially in Frank’s Pflanzenpathologie, p. 530 ff. ; according to these accounts the young germ-tube has the infecting power without previous preparation, and plants of Brassica were at once attacked by the Fungus. The observations may be correct in both cases and the difference may arise from the fact, that several species resembling one another in appearance, but differing in the mode of vegetation, are confounded together under the name of Sclerotinia Sclerotiorum. The discussion of this point would occupy us too long and must be reserved for another occasion. Among other species of Pythium’ which have been carefully examined Hesse’s P, de Baryanum is a parasite on living and healthy plants, and attacks them both with its germ-tubes which are formed in water and with the branches of the mycelium when it has acquired strength. It attains its full development equally well on dead vegetable substances and on the dead bodies of animals, and is therefore equally a saprophyte and a parasite. In the latter character it penetrates into the cells of a great variety of Dicotyledons and Monocotyledons and into the prothallia of Ferns, but leaves plants of Spirogyra and Vaucheria untouched. Some Phanerogams are also said to be secure from its assaults, but this statement requires confirmation. It attacks with especial readiness and frequency the young and watery seedlings of Phanerogams such as the Cruciferae and Amarantus, taking possession of them and destroying them rapidly and completely. Full-grown land-plants are usually less readily attacked and the injury done to them is more local; but they too may be rapidly destroyed by the Fungus if they are placed in water. Other and nearly allied species of Pythium are, as far as is known, partly pure saprophytes, partly facultative parasites within narrow limits. P. intermedium and P. megalacanthum grow as saprophytes on dead parts of plants. They leave living Phanerogams, even young seedlings which are so liable to the attacks of P. de Bary- anum, always and absolutely untouched ; but P. intermedium readily attacks the ? Bot. Ztg. 1881, p- 531. ee ee ae ae ae CHAPTER VII.—PHENOMENA OF VEGETATION.—PARASITES. 38 3 prothallia of Ferns and quickly kills them, while P. megalacanthum was only rarely induced to penetrate into them, and its development in them was slow. Nectria cinnabarina’ is one of the most common saprophytes on dead twigs. Their bright red cushions burst forth in abundance from the rind of branches which have been killed by frost in the previous winter. Their germ-tubes do not attack the surface of living branches, or living rind or bast tissue when laid bare. But if they find their way to a wounded surface where the wood is exposed, they penetrate into it, and the mycelium grows rapidly upwards in the vessels, causing decomposi- tion of the wood-substance ; this is followed by the death of larger or smaller portions of a branch or stem, and the further development and the formation of perithecia by the Fungus then takes place in the dead rind. This at least is the course of proceeding in Acer, Tilia, and Aesculus. Other woods gave an uncertain or negative result. Nectria Cucurbitula, Fr.? developes a mycelium producing gonidia when raised from spores in a nutrient solution. It is uncertain whether this species can arrive at the formation of perithecia in this saprophytic mode of life. But its germ-tubes penetrate through wounds in the /7vzng rind of pines into the living tissue, and spread rapidly through it during successive periods of vegetation, covering a distance of ro cm. in the longitudinal direction in one season; they at last kill the tissues which they have attacked and then form perithecia which come out upon the surface. This highly pernicious Fungus usually makes its attack where wounds have been caused by hail-stones or by fractures under a weight of snow, and especially where the bark has been eaten away by Grapholitha pactolana. Nectria ditissima, Tul., the Fungus which causes canker in deciduous trees especially in the apple-tree*, agrees closely with N. Cucurbitula as regards the arrange- ments which have been described. The Fungus penetrates at some injured spot into the living rind and spreads slowly in it and also in the adjoining wood; the parts attacked are dried up and destroyed so far as they consist of juicy tissue, while cushion-like formations appear all round them advancing centrifugally in successive periods of vegetation ; in consequence of these and of the successive partial drying up of the parts, malformations are produced in the shape of swollen places with a depressed dead centre, which themselves also in course of time partially die away. Gonidia and perithecia emerge from the periderm at the margin of these swollen places where the tissue is still succulent. The wood-destroying Hymenomycetes occupy a prominent position among facultative parasites. Agaricus melleus may be taken first as a typical example of this group. We know from Hartig’s researches supplemented by Brefeld that the spores of this plant germinate on dead vegetable substances and produce the mycelium which is characterised by its strands or rhizomorphous form. This mycelium may develope spontaneously as a saprophyte and bear sporophores in and on dead wood, 1 H. Mayr, Ueber d. Parasitismus v. Nectria cinnabarina (Unters. a. d. Forstbot. Instit. z. Miinchen, III). ? R. Hartig, Unters. a. d. Forstbot. Instit. z. Miinchen, I, p. 88. * R. Hartig, 1. c. I, 109.—R. Gothe in Thiel’s Landw. Jahrb. IX (1880), p. 837. 384 DIVISION III.—MODE OF LIFE OF THE FUNGI. trunks of trees, wooden conduit-pipes, &c. But the strands also make their way from the soil through the uninjured living rind into the roots of healthy living trees, especially our Coniferae; there they destroy the inner rind and then grow at its expense into the subcortical expansions described above, from which hyphae push on further through the medullary rays into the wood. While the mycelium is spreading at these spots and mounting in the stem, it kills the living tissue and ultimately the whole tree. The propagation of the Fungus from tree to tree by means of the mycelial strands spreading far and wide in the soil has been already described. The symptoms of disease which precede death in fir-trees are known as ‘ restn-flux’* (‘ Harzsticken, Harziiberfiille’) and the phenomena attending the decomposition of the wood, which advances with the spread of the Fungus, should be learnt from Hartig’s excellent descriptions *. Trametes radiciperda of Hartig (Polyporus annosus, Fr)., which attacks the wood of fir-trees from the roots and kills it, comes nearest to Agaricus melleus in its mode of life and operation, but it has not the rhizomorphous strands. The filamentous mycelium penetrates from without into the uninjured rind of the roots, whether it has developed directly from the spores or, as is most conducive to the spreading of the Fungus, has grown out of an infected root in moist soil and has encountered a sound root in contact with the first. It has been observed to put out germ-tubes capable of infecting in less than twenty-four hours in a moist environ- ment. Whether it can arrive at its full development when growing as a pure saprophyte on dead wood is still uncertain, but according to some observations of Hartig it is probable ; at any rate it would appear to be adapted rather for strict than for facultative parasitism. R. Hartig has also made us acquainted with a number of other Hymenomycetes which produce decompositions of the wood of iiving trees in forms varying with each species, and thus kill the plants; Trametes Pini, Polyporus fulvus, P. vaporarius, P. mollis, and P. borealis in fir-trees ; Hydnum diversidens, Thelephora Perdix, Poly- porus sulphureus, P. igniarius, P. dryadeus, and Stereum hirsutum in the oak. It is probable that there are many other wood-destroying Fungi which approach the above in the qualities just indicated. All these Fungi attack the wood from places exposed by wounds and do not penetrate into it through the uninjured rind, with the exception of Polyporus mollis, in which this point has not yet been cleared up. It is probable therefore that they are fed and made capable of infecting chiefly by the products of the decomposition of the superficial wound-layers which have been laid bare and killed, in the same way therefore as the Sclerotinieae are facultative parasites; but no satisfactory experiments have been made to ascertain this point. On the other hand it is tolerably certain that Stereum hirsutum often attains to its perfect development as a saprophyte in dead wood. We have no certain knowledge on this point in the case of the other species which have been named. (There appears to be in use no English equivalent of the expression Harzsticke and Harziiber- fille; the word resin-flux is therefore introduced as indicating a prominent symptom of the disease, although it is not an exact rendering of the German terms.] 2 See above, page 23. CHAPTER VII.—PHENOMENA OF VEGETATION.—PARASITES, 385 4. Obligate Parasites. Section CIX. Most of the groups described in Chap. V contain a large number of Fungi which are obligate parasites, as will be seen by reference to the accounts there given; but within the class itself we meet with every gradation of adaptation, from the strictly parasitic mode of life to arrangements in which we may almost as well speak of facultative parasites, as of obligate parasites which are at the same time facultative saprophytes. Phytophthora omnivora’ in the group of the Peronosporeae well exemplifies the transition from facultative parasitism. This Fungus is a destructive endophyte in many kinds of living Phanerogams, as Fagus and especially in young seedlings, in Sempervivum, the Oenothereae, and others. Other species of Phanerogams it leaves uninjured, as Solanum tuberosum particularly and Lycopersicum. Its development is rapid in proportion to the amount of water contained in the host, even when that amount exceeds the limits of a normal and sound state of the plant and becomes pathological, as when the land- plants just named are immersed in water, The development of the Fungus culminates in the formation of oospores, usually in large numbers, after the host has been killed by its assailant. ‘The Fungus can also grow on dead organic, even animal, bodies in water and form an abundance of gonidia, but without arriving, as far as is known, at the formation of oospores. On this latter account it is better to place it among facultative saprophytes. ‘The same may be said of its nearest relative Phy- tophthora infestans the Fungus of the potato-disease, with the limitation that the adaptation to a parasitic mode of life is more marked. For the same reasons the members of the Mucorini, Piptocephalis, Synce- phalis, and Chaetocladium, to which the expression facultative parasites was first applied, may be termed facultative saprophytes. ‘They may be grown as saprophytes from spores in a nutrient solution and produce an abundance of gonidia, but according to present observations they only attain to their full development in the formation of zygospores when they live as parasites on other Mucorini in the manner described in a former page. The species also of the Ustilagineae (see page 179), in which the young plants can vegetate by sprouting or in the manner of the Hyphomycetes in solutions made from organic bodies, must be termed facultative saprophytes. But the saprophytic faculty is much less important to them than the parasitic mode of life, for it is as parasites only that they are able to produce the resting spores and sporophores which are peculiarly characteristic of their development. ‘This is so, even if the round cells of intercalary origin obtained by Brefeld® in large quantities from the mycelium of Tilletia Caries, when it is grown as a saprophyte in nutrient solutions, really have the characters of resting-spores; this can only be proved by observing their germination, and in default of this observation it remains unproved; moreover the characteristic sculpture on the surface of the spore-membrane of T. caries ‘could not be clearly seen’ on the products of cultivation. In the majority of the species which have been examined the saprophytic development does not go beyond the 1 Bot. Ztg. 1881, p. 585. ? Hefepilze, p. 159. [4] cc 386 DIVISION III,—MODE OF LIFE OF THE FUNGI, production of gonidia; and it may be assumed, though it has not been yet distinctly proved, that they may form germs capable of infecting, and that by means of these germs they attack the host-plant and thus return to a parasitic life, somewhat in the way described at page 373 in the case of Cordyceps. The facts stated in pages 265, 339 show that the behaviour of Exoascus and Exobasidium is quite similar to that of the Ustilagineae. The example of Cordyceps leads to the mention of Claviceps, and Epichloe typhina also approaches near to. the latter genus in the points in question. The gonidia (and possibly also the ascospores) of these Fungi may develope small mycelia producing fresh gonidia in the manner described on page 227. That this facultative saprophytism in its various degrees is a frequently recurring phenomenon in parasitic Ascomycetes is to be expected, though more stringent proof of it is in most cases still to be desired. Of all the Ascomycetes the Lichen-fungi, according to our present knowledge, must be mentioned first as examples of strictly obligate parasites, after them the Erysipheae and Polystigma (section LXIII). It has still to be ascertained what are the exact conditions in this respect in the large number of parasites in the groups of the Hysterineae and Phacidieae. ‘The Peronosporeae also contain excellent examples of the class which we are considering, for most species of Peronospora and all of Cystopus are strictly parasitic, the first stages only of germination being completed outside the host. This is the case also with Protomyces. and many Chy- tridieae, some of which even commence germination on the surface of the host (see Chapter V). Lastly, only the strictest parasitism is known in the group of the Uredineae so rich in forms; they germinate if sufficiently supplied with water, and their further development takes place only on the proper host.. Section CX. The Fungi which are parasitic on plants naturally exhibit within the limits of the chief phenomena of parasitic vegetaticn and its effects, which were pointed out on page 359, a variety of special adaptations in respect of their choice of a host and their spreading in, upon, or along with it. The reaction of the host itself which varies in each case corresponds again to the spread of the Fungus. We call attention to the following facts which are of general interest in relation to these points, again referring the reader to the former sections of this work and to the special literature of the subject. As regards the choice of the species to serve as a host, the rules stated on page 359 are of the first importance. Most parasites living on plants require a single proper host for the completion of their whole course of development, though they may enjoy a larger or smaller room for choice between different species more or less nearly allied to one another. Of all the hosts that are possible for a species of Fungus some may be more favourable to their development than others. Cystopus cubicus for example flourishes and forms abundance of gonidia on the leaves of species of Trago- pogon, Podospermum, and Scorzonera, but forms oospores almost exclusively on Scorzonera, especially on S. hispanica; oospores are extremely rare on Tragopogon in-my experience. So it is with the Uredineae and species of Erysiphe. The best known Erysiphe is the Fungus of our grape-vine' which in Europe only forms gonidia * See De Bary u. Woronin, Beitr. III. CHAPTER VII.—PHENOMENA OF VEGETATION.-—PARASITES. 387 (Oidium Tuckeri, Brk.); its sporocarps are perhaps the objects described as Uncinula spiralis, which grow in North America on a native vine. This dissimilar promotion by hosts of different species of the otherwise similar course of development of the Fungus makes no difference in the phenomena in question. Parasites which go through their whole course of development on a single host of a particular species are termed autoectous or auloxenous. All the parasites described in preceding chapters are examples of this class, with the exception of one group to be named presently. _ It is not perhaps altogether superfluous to remark, that the larger part, or at any rate very many species, of the Uredineae, in which the alternation of generations is most copiously differ- entiated, are autoecious. Thus the entire development of Uromyces Phaseolorum is completed on species of Phaseolus, that of U. appendiculatus on the Vicieae, of Puccinia Tragopogonis on > Tragopogon, of P. Pimpinellae on Myrrhis or Chaerophyllum, of P. Falcariae on Falcaria Rivini, of P. Violarum on species of Viola, and so on. The contrary is the case with a number of Uredineae which form aecidia. These are obliged to change their host with the separate sections of their alternating genera- tions in order to complete the course of their development, like the Cestodes and other parasitic worms. They are accordingly termed heferoectous, or still better metoectous or metfoxenous as changing their place of habitation or host’. I was myself the first to establish this metoecism in the case of Puccinia graminis, in which the phenomenon or at least its consequences were recognised more than a hundred years ago by agriculturists, who rightly maintained against the botanists that grain grown in the neighbourhood of shrubs of Berberis were liable to be attacked by rust, that is by Puccinia graminis. ‘This parasite exhibits the pleomorphism and alternation of generations of the Uredineae which form aecidia in its greatest variety of form (see page 279). Its teleutospores pass the winter on old stems of wild and cultivated grasses, especially Triticum repens, while the germ-tubes from the sporidia which are developed in the ensuing spring penetrate into the epidermal cells of Berberis vulgaris, more rarely into those of a Mahonia, and never into a grass. They develope rapidly in Berberis into a mycelium which produces aecidia but never forms uredospores or teleutospores, and if the germ-tubes of the aecidiospores find their way into the stomata of suitable Gramineae they develope there and there only into a mycelium which produces uredospores and teleutospores. The germ-tubes of the uredospores in their turn develope only on the Gramineae, and in the manner which is common to all uredospores.. Later investigations have shown that an analogous change of hosts takes. place in many other species. The aecidiaof Puccinia Rubigo vera and P. coronata which also live on Gramineae or Cyperaceae in the other sections of their development are confined, the former to the Boragineae, the latter to species of Rhamnus; those of P. Moliniae to Orchis ; those of P. Caricis to Urtica and of P. (Caricis) limosae to Lysimachia thyrsiflora ; Uromyces Dactylidis forms its aecidia on the leaves of common species of Ranunculus*, and its 1 See on theterminology Bot. Ztg. 1867, p. 264; on other points see the literature of the Uredineae enumerated above on page 286. ? See also Cornu, Comptes rend. 1882, 94, p. 1731. Cc € 2 388 DIVISION III,—MODE OF LIFE OF THE FUNGI, uredospores and teleutospores on Gramineae; Uromyces Pisi forms uredospores and teleutospores on Vicieae and its aecidia on Euphorbia Cyparissias, the well-known Euphorbia-aecidium. Next to these species all the Gymnosporangieae are examples of the phenomenon in question, as Oersted was the first to show from gardeners’ traditions; their teleutospore-layers inhabit species of Juniperus, and migrate to Pyrus and other Pomaceae for the formation of aecidia, which were once known by the name of Roestelia. The aecidia of several species which live on the Ericaceae are formed on leaves of the Abietineae which are entering their first year, those of Melampsora Géppertiana, as Hartig showed, on Abies pectinata ; those of Chrysomyxa Rhododendri, the Fungus of the alpine rose, and of C. Ledi on the spruce, Abies excelsa. The Coleosporium of species of Senecio migrates according to Wolff to the leaves of Pinus sylvestris, and there produces its aecidia which were known by the old name of Peridermium Pini. The rest of the known cases of the kind will be found collected together in Winter’s Pilzflora. The same work also enumerates the forms bearing teleutospores and those bearing aecidia, of which it is known that the germs which are capable of infecting do not proceed to further development on the hosts on which the forms themselves grew. The aecidia-forms never propagate themselves on their hosts; teleutospore- forms are produced only in certain circumstances through the medium of the- uredospores which accompany the teleutospores. From the analogy of the cases in which metoecism is certainly known these forms must be separate sections in the development of metoecious species. Their complete form-cycle has yet to be ascertained. To this group belong on the one hand most of the species of Melam- psora and Coleosporium, the Cronartieae and also Hemileia vastatrix, the Fungus of the coffee-plant, on the other the aecidia of fir-cones, the aecidium known as Peri- dermium elatinum which causes the ‘witches’ brooms’ in Abies pectinata (see page 368), the aecidium of species of Clematis, and many others. Metoecism, that is, enforced change of the living host, is not known outside the group of the Uredineae ; its supposed occurrence in other species has not yet been confirmed. ‘There is another phenomenon which must of course be kept quite distinct from it, and which may be termed “poxeny or deserting the host in opposition to a change of the host. Many Fungi which inhabit plants spend a certain period of their life in strictly parasitical fashion on the host, and then separate from it and complete the other sections of their development independently without a living host, and entirely at the expense of the reserve of food which they have appropriated from the host. The separated thallus may be compared as regards the economy of the metabolism to a ripe spore which is able to germinate at the expense of the reserve of food which it contains. This phenomenon is most striking in Claviceps which continues strictly parasitic up to the ripening of its sclerotia, and produces the stromata from them after they have fallen from the plant under favourable conditions of temper- ature and supply of water in the next period of vegetation (see on page 227). Reinke has recently published an elaborate investigation of the various substances which enter into the composition of the plasmodium of Fuligo*, to which the reader is here referred, The amoeboid movements of the swarm-cells are continued in the plasmodia. They may be seen in larger specimens by continuous observation even with the naked * Sitzgsber. d. Niederrhein. Ges. 4 Aug. 1879. ® Zellbildung u. Zelltheilung, 3 Aufl. p. 79. * Studien ii.d. Protoplasma von J, Reinke u. H, Rodewald in Untersuch. aus d. bot, Laborat. d. Univers. Gottingen, II, Berlin, 1881. 426 SECOND PART.—MYCETOZOA. eye. The microscope reveals a constant change of outline in all the branches, some- times in the form of a slight undulating movement, sometimes of an unceasing protrusion and withdrawal of small pointed tentacle-like processes or pseudopodia. Some of these pseudopodia or single flat projections of the main branches swell into a knob at the free extremity and presently grow into larger branches, while in another part branches diminish in size and gradually sink back into the main stem. Here two branches grow out towards each other till they touch one another, and then coalesce and anastomose; there a branch becomes constricted at some point and divides into two. By these processes a plasmodium may separate into several parts, and several plasmodia may be united into one; but according to Cienkowski’s and my own observations union never takes place between plasmodia of different species. Branches of every degree and every size participate in the movements, and the smaller the branch the more active is its movement. The alternation in the movements takes place at all points alike in the plasmodium, but the protrusion of branches predominates on one side, the retraction on the opposite. Hence there is often an active advancing movement, a locomotion of the plasmodium in the direction of the greater protrusion, and the anterior portion of the whole body which leads the way in the advance assumes the form of a system of branches with swollen extremities, which spread out like a fan and are connected together into a reticulated structure by numerous and constantly changing anastomoses; in other words it becomes a flat surface pierced so as to form a sieve or net and traversed by the stronger branches like swollen veins, its margin being thickened and uneven (Fig. 185). The inner substance of the plasmodium is also subject to a variety of active movements and displacements which are seen to be directly connected with the amoeboid movements, but sometimes appear to be independent of them. First there are the previously mentioned swellings and sinkings of the marginal hyaloplasm, the locality of which is constantly changing. Secondly stream-like displacements of the _inner granular plasm with change of speed and direction. The varying breadth of the marginal hyaloplasm shows that there is a constantly varying pressure of the granular mass in the direction of the periphery. ‘The movement in the interior takes place in the form of streams which occupy the whole breadth of a branch, or run in narrow threads through the surrounding substance which is apparently motionless. The movements are chiefly directed towards the swelling and advancing extremities of the branches, into which the granular mass streams in, the alternating backward flow being weaker and less copious. The reverse takes place in branches which are being withdrawn. But movement and streaming may be constantly alternating with rest in the interior of the plasmodium without this prevailing and directly perceptible connection with the amoeboid change of shape. Further details with respect to these phenomena must be sought in monographs and in the physiological treatises which have appeared since my first work on this subject. See also below in section CXXVII. The surface of the plasmodia of the Physareae which I have examined is covered with a soft shiny envelope, which is not distinctly defined on the outside but is quite distinguishable from the marginal layer. It forms a border round the thicker branches which is often more than 0,o1 mm. in thickness, and is in itself colourless and pellucid but is often covered with small particles of soil which adhere to it. ee es eee ee es ee ee ee eee eC erm eee aaa CH.VIIIT.— MORPHOLOGY AND COURSE OF DEVELOPMENT.—MYXOMYCETES. 427 It consists of a sticky substance which swells in water and contracts in alcohol and is scarcely coloured by iodine, and must therefore be different from protoplasm. It passively follows the movements of the plasmodium. Portions of it often remain adhering in the form of thin films of mucilage to spots from which a plasmodium has moved away. This envelope is often very thin round the rapidly swelling extremities of the branches, and cannot be distinguished at all round slender pseudopodia, having been either pierced through by them or extenuated by their advance till it is no longer perceptible. The plasmodia of the Stemoniteae, Trichiaceae, Ceratieae and Lycogala have in the main the same structure and power of movement as those of the Physareae, but they never have the granules of calcium carbonate and therefore usually appear to be much more finely granular than in the Physareae. The dark-blue or violet-brown plasmodia of the Cribrariae and Dictydium contain large brown granules of some organic substance, but have as yet been very insufficiently examined. The plasmodia of Lycogala which live in rotten wood are surrounded by a thick colourless membrane; I observed a similar membrane some time ago in Arcyria punicea. It is not yet ascer- tained how this membrane behaves in the movements. I was unable to see it in former years in specimens of Lycogala grown in water. I found the plasmodia of Stemonites fusca, when it issues from the substratum to form its sporangia, surrounded by a stout envelope, the inner and thicker layer of which is coloured a dark blue by iodine while an outer thin layer remains colourless. All the plasmodia last mentioned are inconspicuous bodies, the stouter branches of which in Arcyria punicea are not more than 16 p in thickness, in Lycogala not more than 24 yw. They live for the most part in the interior of rotten parts of plants, especially rotten wood, and are not visible to the naked eye till they come to the surface to form sporangia, Section CXX. Transitory resting-states, Those stages of the development in Myxomycetes which have the power of motion are able to pass into resting-states and to return again under favourable conditions to the state of movement. Three resting-forms are at present known: mucrocysts, thick-walled cysts (Cienkowski) and sclerotia. It appears from cultures of Chondrioderma difforme that these transitory resting-states are not necessary members of the course of development. Their formation would seem to take place only when the development of the swarm-cells into plasmodia or of the plasmodia into sporangia is interrupted by insufficiency of food, by slow desiccation, or by slow cooling to below a certain minimum. But there are a number of observations which also point to other at present unknown causes. The state of movement is restored when the bodies after desiccation are again placed in water of the proper temperature. The term microcyst was given by Cienkowski to the resting-state of the swarm- cells. Under the conditions above mentioned these cells assume the form of spheres which are smaller than the spores and are surrounded by a very delicate colourless membrane, as in Perichaena liceoides according to Cienkowski, or are without a membrane but provided with a. very firm marginal layer. In other respects their structure remains the same as that of motile swarm-cells, only that the vacuoles in many cases disappear and the protoplasm becomes more dense. The swarm-cells of Didymium praecox and D., difforme encysted in this way and perfectly dry retain 428 SECOND PART.—-MYCETOZOA. their vitality for more than two months ; how soon life becomes extinct in them has not been ascertained. If placed again in water, they return to the motile swarming state, and the more quickly the shorter the period of desiccation. Those of Perichaena liceoides cast off their outer membrane under these conditions. The thick-walled cysts and sclerotia are résting-states of plasmodia. The former were examined by myself in isolated cases in Fuligo, and Cienkowski followed them through the whole course of their development in Perichaena liceoides. The cysts were formed by young plasmodia in both species. According to Cien- kowski’s observations the plasmodium divides by the rending of its branches into pieces of very unequal size, which draw in their processes and assume the shape of smooth spheres. ‘Then a membrane of considerable thickness forms on the surface and becomes rough and wrinkled and assumes a dark-brown colour. Within this membrane the protoplasm contracts still more and forms on its surface a second coat with a double-contour. If placed in water after drying for several weeks the round bodies remain first of all unchanged for some weeks, and then the protoplasm begins to display slow undulating movements and at length swells up, makes a hole in the surrounding coats, and slowly emerges from them with all the characters of a plasmodium. The sclerotia are the resting-states of full-grown plasmodia. They have been observed in Didymium leucopus and D. difforme, D. Serpula, Fuligo, Physarum sinu- osum, Perichaena liceoides and in a number of Physareae which have not been more precisely determined, and perhaps also by Corda in Stemonitis*. Some of them are the forms on which Persoon based his fungal genus Phlebomorpha. When their formation begins the plasmodium draws in its slenderer processes and assumes the shape of a sieve-like plate, or in Fuligo of a small tuber a few millimetres in diameter and with irregular prominences on its surface ; the granules become distributed uniformly through the fundamental substance, the solid ingesta are extruded, the movement gradually ceases, and the whole body breaks up into an innumerable quantity of roundish or polyhedric cells with an average diameter of from 25 to 40. The body becomes at the same time of a wax-like consistence and dries into a brittle horny mass, resembling the sclerotia of many Fungi. Each cell chiefly consists of a firm protoplasm which incloses vacuoles varying in size and number, and a pigment and granules distributed in the same manner as in the motile plasmodia, and shows a sharply limited marginal layer. Nuclei are there no doubt, though they have not as yet been observed. In the strongly developed sclerotia of some species (Fuligo, Didymium Serpula) the protoplasm is surrounded by a distinct colourless membrane, which in both the species mentioned shows the reaction of cellulose with iodine and sulphuric acid or with Schulze’s solution, The membranes are firmly attached to one another, either immediately or, as in Fuligo, by a homogenous intermediate substance which softens in water. In small weakly developed specimens of the above species and in all sclerotia that have as yet been examined in other species, as for instance in Didymium difforme, no distinct membranes can be seen round the protoplasm. ? Icon. Fung. II, Fig. 87 4. oe CH.VIIT,— MORPHOLOGY AND COURSE OF DEVELOPMENT.—MYXOMYCETES, 429 The outer surface of the sclerotia is usually covered by alayer of the same homogeneous substance with a capacity for swelling which is found between the cells’ in Aethalium. Upon it there are also in many cases (Fuligo, Didymium) scales or grains or crystals of calcium carbonate which must have been excreted during the formation of the sclerotia. If a mature and dry sclerotium is placed in water it at once swells up, and its cells coalesce once more into a motile plasmodium often in from six to fifteen hours, in older specimens after a longer interval which may last some days. Where membranes of cellulose are present they are first dissolved. The process begins at the surface and advances towards the centre. If single cells of a sclerotium are watched, contractile vacuoles are seen to form in them a few hours after they are moistened, and protrusion of motile branches and pseudopodia and the creeping forward movement all begin as in plasmodia. Where moving cells meet and touch they coalesce; if moving cells encounter cells that are still at rest, they absorb them. In this way a large plasmodium is gradually formed containing many sclerotium-cells which it has engulphed. These phenomena, which were first observed by Cienkowski in Didymium difforme, explain the formation of the plasmodium from the compact sclerotium. In plasmodia recently formed from sclerotia in which the cells have not separated from one another we always see a number of unaltered or evidently dead sclerotium-cells carried along by the stream of granules ; these become presently less frequent and at length entirely disappear ; they must therefore be either dissolved or they coalesce with the substance of the plasmodium. Sclerotia are known to retain their vitality in a dry state for 6-8 months. Fuligo and Didymium Serpula are known from several direct observations to persist during the cold and dry season of the year in the condition of a sclerotium, and pass again into the motile state with damper and warmer weather. Vitality did not last more than 7-8 months in most of the observed cases, though sclerotia of Didymium Serpula lived more than a year (others only 7 months), and Léveillé ? quotes an obser- vation to the effect that.a sclerotium of a Myxomycete had been known to return to the motile condition after having been kept for 20 years. Section CXXI, Development of sporophores and sporangia. ‘The de- velopment of the plasmodia closes with the formation of spores within receptacles, sporangia, or on the outside of sporophores. The latter are confined to the Ceratieae, the former are common to the rest of the Myxomycetes. We may therefore with Rostafinski distinguish the Ceratieae as exosporous, all other Myxomycetes being exdosporous. The sporangia of the endosporous forms are vesicles, which are usually about 1mm. in height but may considerably exceed that size, and rise with or without a stalk above the substratum or lie upon it in the form of round or flat tubes. Their structure when they are fully formed will be more minutely described in section CXXII, Their development from the plasmodium is divided into the successive sections of forming, dévelopment of wall, separation of the spore-plasm, and lastly ? Ann. d, se. nat, sér. 2, XX, p. 216. 430 SECOND PART.—MYCETOZOA, Sormation of the spores and of the capillitium which in many genera accompanies the ‘spores. These processes also have been most thoroughly and satisfactorily examined in the lime-containing Physareae, Rostafinski’s Calcareae, and will be described from them in this place. In the simpler cases of forming of sporangia, which we may examine first, either an entire plasmodium spread out on its substratum becomes transformed into a sporangium, or it divides into a number, often a large number, of pieces, each of which suffers transformation. This transformation is the result of the same kind of amoeboid movement of the protoplasm as that which causes the change of shape and place in the vegetating plasmodium, with the difference only that in the forming of sporangia the masses of protoplasm by drawing in their branches become constantly broader and rounded off and at length assume stable forms. The spor- angia which lie flat on their substrata are in conformation simply portions of a plasmodium which have been thus contracted and thickened. Erect sporangia on a narrow or stalk-like base begin as node-like swellings on a branch of the plasmodium, and gradually rise to their ultimate form as the surrounding protoplasm flows into them and assumes an upward direction. The soft envelope which surrounded the retracted branches of the plasmodium remains sticking to the substratum and there dries up; but there appears in its place round the young sporangium a firm membrane evidently produced by its further growth, and this membrane constitutes the wall of the sporangium which often grows to a considerable thickness, In the stalked forms the sporangium-wall begins to strengthen and get firm at the base of the stalk, and the process advances upwards. The zones of the membranes successively growing stronger serve as a support for the upward moving protoplasm. During the forming of the sporangia the solid ingesta which are present in the plasmodium begin to be expelled from it. When a sporangium has assumed its definitive form the spore-plasm is separated off inside it. The granules of calcium carbonate, the pigment and perhaps other substances also, which at present are not precisely determined, are eliminated from the true protoplasm. In Physarum and its nearest allies they move to the wall and become imbedded in it or attached to it; or they collect into lumps of various shapes which are arranged differently inside the sporangium in different species, and by the formation of a membrane round them are soon converted into vesicles containing calcium carbonate or pigment (Fig. 191). In Didymium and the forms nearest to it the calcium carbonate granules in the plas- modium are dissolved and in this state are expelled from the sporangium, and while the granules disappear inside, the outer surface becomes covered with crystals of the salt. In Didymium Serpula the only well-known species of this group with coloured plasmodia, the yellow colouring matter is gathered up at the same time inside the sporangium into round lumps, which are then inclosed in pigment-vesicles by the formation of membranes round them. The protoplasm which remains after these substances have been removed from it is for the most part a colourless body with small granules uniformly distributed through it. By staining numerous nuclei are made visible in it. This plasm has been termed spore-plasm, because much the larger part of it is used for forming spores; as soon as it has got rid of the foreign substances in it its nuclei rapidly increase in number, and at length the whole mass divides simul- CH.VIIT,—MORPHOLOGY AND COURSE OF DEVELOPMENT.—-MYXOMYCETES, 431 taneously into polyhedral portions with rounded corners, each of which encloses a” nucleus, and becoming invested with a firm membrane ripens intoa spore. The spores when first formed are somewhat larger, never smaller, than when they are mature. A comparatively small portion of the spore-plasm is expended in forming the capiliiiium, a filamentous structure to be described more fully in section CXXII, which spreads through the cavity of the sporangium and is connected both with the wall of the sporangium and with the vesicles containing pigment and calcium carbonate, The capillitium always appears before the spores, and all the parts in the earliest state in which they have been examined are seen to be formed and arranged exactly as when they are mature, only they are at first extremely delicate and gradually acquire their subsequent firmness. These points will be noticed again below. Fuligo, the ‘ flower of tan,’ agrees with Physarum in all other points, but shows a variation in the phenomena described above in the forming of the sporangia; here a number of plasmodia collect together from every side and become fused together into a narrow dense reticulum with the shape of a cushion, which may come to be twelve inches in breadth and one in thickness or may remain quite small. The strands of this reticulum anastomose in every direction with one another. Then all the spore-plasma passes after its separation into the inner portion of the reticulum which swells proportionately, and then acquires the structure of the sporangia of Physarum; the vesicles with calcium and colouring matter remain behind in the peripheral layers, where they collapse and dry up forming a calcareous crust or rind from one to several millimetres in thickness. Of the rest of the endosporous Myxomycetes, those, that is to say, which do not belong to the Physareae, it may be confidently affirmed that the development of the sporangia from the beginning of forming is thoroughly like that which has just been described. ‘The development of the spores is in all cases the same. Strasburger succeeded in following the multiplication of the nuclei, which precedes the formation of the spores, in Trichia fallax through all stages of the division, and ascertained their morphological agreement with the divisions of the nucleus in many other vegetable and animal cells. The case is the same also with the formation of the capillitium, with some limitations naturally arising from generic differences. The elimination of contained substances which leads to the formation of the spore-plasm is less copious or there is none at all to be seen, as is the case in Stemonitis in all states which have at present been examined, because the substances secreted in the one case are wanting from the first in the other. The very first stages in the forming of sporangia are in most instances imperfectly known because of the difficulty of procuring plasmodia in the vegetating state. What is known of it in most genera with simple sporangia, as Trichia, Arcyria, Dictydium, &c., corresponds with the fore- going description of the Physareae. On the other hand the large and often thick- walled spore-receptacles of Lycogala, Reticularia, Lindbladia and others are formed by such an accumulation and intermingling of numerous plasmodia as has been described in the case of Fuligo.. Rostafinski applies the collective name aethalium to all bodies which originate in these combinations of plasmodia. Little more is known of the processes of differentiation in their development than can be concluded from the mature state, 432 SECOND PART.—MYCETOZOA4, The conformation of the sporangia in Stemonitis runs differently in one respect from that of all other known forms, The slender threads of the plasmodium, which lives in rotten wood, unite at first into large cylindrical or ellipsoid bodies of homogeneous protoplasm, which rest their broad surface on the substratum. Then a hollow cylindrical firm central column is separated off in the protoplasmic body, and rises vertically from a membranous base resting on the substratum, advancing by acropetal growth (Fig. 186 a, 4). The mass of protoplasm, the longitudinal axis of which is traversed by the column, stretches at first at the same time in the same direction ; but it afterwards loses hold of the substratum at its base and clinging to the central column moves on it a certain distance upwards till at ites ais alts FIG. 186. Stemonitis ferruginea. @ a com- FIG. 187. Ceratium hydnoides. Forming of mencing sporangium with the first beginning of the sporophores on plasmodia which have come to the central column. 4 sporangium which has reached surface of a piece of wood. Successive stages of its mature form, capillitium and spores not yet formed. development according to the letters a—c; c the Both figures represent specimens in optical longitu- mature state. After Famintzin and Woronin, about dinal section hardened in alcohol and then rendered 3 times the natural size. transparent in glycerine. amagn.12times, 4 15 times. length it becomes stationary and developes into a sporangium in the usual manner (Fig. 186 4). The sporangium is supported on the lower portion of the central column which is laid bare by the upward movement of the protoplasm, as on a stalk. Other genera allied to Stemonitis behave in a similar manner, Further details must be sought in the different monographs. The plasmodia of the ectosporous Ceratium hydnoides come forth to the surface from the interior of the rotten wood which is their habitation to form their spores (Fig. 187). Here they appear at first to the naked eye as white cushion-shaped bodies (Fig. 187 @); examination with the microscope shows that these cushions are formed of countless microscopically slender plasmodium-branches, united together in every direction into a net-work of narrow meshes, such as is shown in Fig. 188 a. The meshes are filled with a hyaline homogeneous gelatinous substance of watery consistence, which forms a thin coating on the surface of the net-work. To form the sporangia cylindrical often dichotomous outgrowths, resembling the spikes of a Hydnum and growing to be a few millimetres in length, rise erect from the surface of the cushion (Fig. 187 4, c). The whole body of protoplasm moves into these outgrowths, leaving only @ thin flat layer to connect it with the substratum. During Mash ae oa ee CH.VIII.--MORPHOLOGY AND COURSE OF DEVELOPMENT .-—-MYXOMYCETES. 433 these movements the branches of the plasmodia all change their previous distribution through the whole of the thickness of the body and creep to the periphery, where they form a net-work stretching only in the direction of the surface and formed of threads which become successively broader and meshes growing narrower and narrower (Fig. 188 a). The whole is covered on the outside by a thin layer of the hyaline protoplasm which alone forms the whole of the inner portion of the body. When these processes are completed, the net-work of protoplasm breaks up simultaneously into numerous polyhedral portions of nearly uniform size (Fig. 188 4), They contain each a nucleus, become flattened from without inwards, and remain grouped in a simple layer which follows the surface like an epithelium. Then each of these proto- plasmatic bodies begins at once to grow convex towards the outside, and to lengthen out at right angles to the surface of the whole body into the shape of a sphere borne on a slender conical stalk (Fig. 188 4). A delicate membrane is formed at the same time within which all the protoplasm passes through the stalk into the spherical expansion at the extremity. The latter then becomes in- vested all round with a some- what thicker membrane with an ellipsoid outline, and thus becomes a mature spore which is readily detached from the empty hyaline stalk. The entire gelatinous sporophore under- goes no further changes, but in most cases soon dissolves and disappears, The other known ecto- > FIG. 188. a@ Ceratium hydnotdes Piece of a sporophore in the act of forming : sporous Myxomycete,Ceratium the branches of the plasmodium in the upper part are already beginning to be ° porioides, is distinguished from pdt 7 Sp obese «4 ha babel spoeamuatli’s & eaniee tation . e ° which subsequently become slightly ellipsoid, on their stalks. After Famintzin and the species just described only Woronin. @ magn. about 68 times, 6 120 times. by the yellow colour and by the shape of its sporophore, which resembles in form the hymenium of a Polyporus (see page 288). The development of the sporophores and receptacles as just described runs its course rapidly if the conditions are favourable. According to a series of observations on spontaneously developed Physareae, species.of Trichia, Stemonitis and others, the complete development from the commencement of the formation to maturity requires an interval on the average of about 12 hours; the development is quicker or slower in particular species, or according to the temperature and moisture of the environment. The sporophores of Ceratium are perfectly formed according to Famintzin and Woronin in the course of a summer night. The entire development of the species may also be accomplished very rapidly. Cienkowski obtained in four days fully formed plasmodia of Chondrioderma difforme when grown on microscopic slides, and these formed sporangia on the fifth day. : [4] Ff 434 ; SECOND PART.—MYCETOZOA, Delay may of course occur where the conditions are unfavourable. ‘That the several species behave very differently in these respects is shown by the fact, that many of them, Trichia rubiformis, T. clavata and T. varia for example, are observed to form their sporangia almost entirely during a short portion of the yearly period of vegetation. The biological relations of most of the species require further examination. Section CXXII. The structure of the mature sporophores is n all cases essentially the same as in the Ceratieae. The ripe sporangia in the majority of the endosporous genera, which show a great amount of variation in different species, must be described from a few of the typical forms, which have been known for some time. For special peculiarities the reader is referred to monographs and especially to that of Rostafinski. We must first distinguish between the smple sporangium, which proceeds from one plasmodium or from a part of one plasmodium, and the ae‘halium, as Rostafinski understands that term, which is formed from large combinations of plasmodia. 1. It has been already said that the mature sporangia in most Myxomycetes are round or elongated, stalked or sessile vesicles one to a few millimeters high ; less frequently, as in Didymium serpula, Trichia serpula and Licea flexuosa, P., they are cylindrical or flattened tubes forming a network and lying on the substratum. The wall of the sporangium is formed of a membrane which in constitution re- sembles the cellulose-membranes of plants, It is either a structureless hyaline and FIG. 18, Didymium squamulosum, AS. (D. leucopus, Fr.) A ripe sporangium divided longitudi sometimes, as in Diachea and some species near the middle with the spores removed. Magn. about . 25 times. of Physarum, an extremely delicate mem- brane, or it is thick and firm and evidently stratified, as in Leocarpus vernicosus, Craterium, Trichia varia and others; in the Physareae included in the old genus Diderma it is even double, that is, it is differentiated into two layers which may be easily separated from one another and which do often separate of themselves, Projecting thickenings of different dimensions in the shape of warts and ridges occur in some cases, on the whole of the surface for example of the thick olive-brown outer layer of Lieea flexuosa, and on the inner surface of the base of the sporangium of Arcyria incarnata, A. punicea and A. nutans. The whole of the inner surface of the membrane in Cribraria and Dictydium shows projecting thickenings in the form of flattened ridges connected together into a delicate net-work. The membrane is colourless or coloured in various shades of violet, brown, red and yellow according to the genus and species; itis usually continued at the point of attachment of the sporangium into an irregular membranous expansion formed of the dried envelopes of the plasmodium, and securing the sporangium to the substratum. The stalks, except in the Stemoniteae, are tubes usually with a thick wall, which is wrinkled and folded lengthwise and is continued above into the wall of the sporangium, Its lumen is either in open communication with that of the sporangium, ve Law Me oe er ee CH,VIII.—-MORPHOLOGY AND COURSE OF DEVELOPMENT,—MYXOMYCETES. 435 as in Trichia and Arcyria, or is separated from it by a transverse wall; if the septum is convex upwards it is termed the co/umella or central column (Fig. 189). The cavity of the stalk varies in breadth in different species and contains nothing but air, as in Physarum hyalinum, or is filled in the manner which will be described below. The structure of the membrane of the sporangium in most of the species which contain no calcium, Licea, Perichaena, Cribraria, Arcyria, Trichia, &c., is usually such as has now been described. In some of these it also contains coloured granules of an organic substance, the nature and origin of which have yet to be ascertained; these granules are imbedded in the stronger ridges of thickening matter in Cribraria and Dictydium ; in Perichaena liceoides they lie singly or in groups on the outer surface. The olive-brown outer layer of Licea flexuosa shows an irregularly granular structure throughout the entire thickness. FIG. 190. “Physarum leucophaeum, Fr. a@spor- FIG. 191. Physarum leucophaeum, Fr. Piece of the wall of a angium seen from without. 4 sporangium divided sporangium with tubes of the capillitium attached and spread out in in half and the frame-work of the capillitium water; @ points of attachment of the tubes of the capillitium; 4 calcium exposed by removal ofthe spores, Magn. 25 times. carbonate-vesicles; to the right on the margin a calcium carbonate- vesicle on the wall. The rest of the wall is covered with calcium carbonate-granules singly or in groups. Magn, 390 times. On the other hand the wall of the sporangium in most of the Physareae and their allies (Calcareae of Rostafinski) is incrusted, wholly or in part according to the genus and species, with the calcium carbonate eliminated in the separation of the spore- plasm. In a number of genera, of which Physarum may be taken as a representative (Figs. 190, 191), the calcium carbonate appears in the form of small round granules which either lie isolated and more or less deeply sunk in the wall, or form dense irregular accumulations on its inner surface. In many species the granules of calcium carbonate, especially those that are collected together in heaps, are surrounded by the extruded colouring matter mentioned above, which is yellow in Physarum aureum, P., Ph. sulphureum, A.S. and other species, or more rarely reddish-yellow as in Ph. Ff 2 436 SECOND PART.—-MYCETOZOA. psittacinum, Ditm, The heaps of granules appear in this case to the naked eye as small coloured patches or warts on the dry sporangium; where there is no pigment they are white. Didymium (Fig. 189) is distinguished by a crystalline covering of calcium carbonate like hoar-frost formed of stellate glands and small single crystals on the outer surface of the sporangia. ‘The Diderma-forms mentioned above, which partly approach Physarum and partly Didymium, have the wall of the sporangium differ- entiated into a delicate inner layer which is free from or contains very little calcium carbonate, and an outer layer, a brittle incrustation of lime, consisting of round or crystalline fragments of calcium carbonate closely crowded and held together by a small quantity of organic matter, which when the calcium carbonate is dissolved remain behind as a delicate membrane. “Calcium carbonate eliminated from the plasmodium in a granular or crystalline form is imbedded in unusually large quantities in the basal wall of sessile sporangia and in the wall of the stalk in stipitate sporangia in many of the Calcareae. In the latter case a considerable amount of the salt often occurs inside the stalk and columella, where it is not unfrequently associated with irregular lumps of some organic substance and to a great extent fills up the cavity as in Didymium leucopus, Fr. (Fig. 189) and Diachea. The cavity of the-sporangium is either filled exclusively with the numerous.spores, as in Licea and Cribraria, or, as in most genera, tubes or threads of different forms occur between the spores and constitute the capz/iium, The capillitium of Physarum and its nearest allies (Figs. 190, 191) consists of somewhat thin-walled non-septate tubes which spread their branches in every direction and combine them into a net- work. Many branches run from the periphery of the net-work to the wall, and are firmly attached to it by their usually funnel-shaped extremities. The tubes are swollen and inflated at the nodes of the net-work, forming the calcium carbonate-vesicles mentioned above and sometimes also containing a pigment. All the Calcareae have a capillitium which is everywhere firmly attached by the extremities of its branches to the wall of the sporangium in the manner here described. In Didymium (Fig. 189), with which genus Spumaria and Diachea agree in this respect, the capillitium consists of very slender threads, from 1-3 to 2m in breadth in D. nigripes, Fr. and D. leucopus, Fr., as much as 2-4 » in D. farinaceum, which are cylindrical or slightly flattened, solid or with an indication of a cavity in the form of a single line in the longitudinal axis, and usually of a dirty violet-brown colour in the broader parts. The threads are usually quite free from calcium carbonate; in a few cases, as in D. physaroides, they inclose single angular granules or crystals of calcium carbonate. They run in Didymium from below upwards most commonly straight or sinuous in a radial direction from the insertion in the stalk to the upper and lateral wall, their anastomoses usually forming an acute angle. D. Serpula is remarkable for the numerous round pigment-vesicles which adhere to the threads of the capillitium, and like the spores have a violet- brown membrane, but are from four to six times their size, being sometimes 5°p in diameter. - The capillitium of the Trichiae and Arcyriae consists of tubular threads which have no deposits of calcium carbonate, and are either not attached at all to the wall of the sporangium or only at a few definite points. In Arcyria (Fig. 192) it is a non- CH.VIIILA— MORPHOLOGY AND COURSE OF DEVELOPMENT.—MYXOMYCETES. 437 septate tube separating into countless branches, which form a net-work by their anastomoses. The thick homogeneous wall has the same colour as the sporangium- membrane, and its outer surface is usually furnished with projections which take the form either of small spikes or warts, or of annular or semi-annular transverse ridges according to the species. In Arcyria punicea and A. cinerea the capillitium is anchored by the blind ends of branches of the net-work which are grown to the lower part of the wall of the sporangium. In most species (A. incarnata, A. nutans) it is nowhere in connection with the wall, but is fastened loosely by a few branches from the tubes, which descend into the stalk and are squeezed in between the cells which fill it up and which will be described presently. So long as the capillitium is inclosed in the sporangium its branches are all bent in every direction and folded up, and the meshes with their four, five or more sides are narrow and irregular. When the sporangium “ Nu 7S se <> 2 oa aE ra S {] Qe, 4 FIG. 192. a, bArcyria incarnata, P. inoutline. a a ripe spor- FIG. 193. a, 6 Trichta fallax, Fr. a half ofa angium closed. 4 the same open with the expanded net-work of capillitium-tube. 4 superficial view of a spore. the capillitium. c¢, @ Arcyria Serpula, Wigd. (4. anomala, De ¢, @ Trichia chrysosperma, DC, De By. ¢ ex- Bary.) ¢ portion of a capilitium. @aspore. @ and 4 magn. 20, tremity of a capillitium-tube. d@ spore. Magn. c and d 390 times. 390 times. opens on reaching maturity, the branches straighten themselves in most species ~ (A. cinerea is an exception), the meshes become broader and the circumference of the net-work many times larger (Fig. 192 a, 4), and the structure never returns in any degree to its original form. The capillitium-tubes of Trichia and Hemiarcyria which have frequently been described are united in the latter genus (H. rubiformis, H. clavata, &c.) into a net-work with branches which at the same time have free extremities, In Trichia (Fig. 193) they are quite free, and either simple or furnished with single short branches, their extremities being usually pointed, and in some species, as T. fallax, long and attenuated. The length of the free tubes varies usually between -3 mm. and 7 mm., the average thickness being from 5 to 7 »; longer and much shorter tubes occur here and there. The transverse section is usually circular. Their contents appear to be pellucid, but 438 SECOND PART.—MYCETOZOA, treatment with potash discloses an axile thread of an opaque substance, which turns yellow with iodine and is a remainder from the contents of the young tubes, The membrane of the tubes is thick but not evidently stratified, with a different degree. of flexibility in different species, and coloured with different shades of yellow, red and reddish brown. It shows in all cases ridge-like projections or thickenings on the outer surface which run spirally round the tubes and often appear as folds in the membranes, since the lumen of the tubes is broader along their course and constricted in the intervals between them. The direction of the spiral as it ascends is with few exceptions, one only of which has come under my notice in Trichia varia, the same as that of the hand of a watch. The number of ridges varies with the species, being 2 in T. varia and 3-5 in T. fallax and T. chrysosperma. Variations of number in the same tube are partly due to bifurcation of the ridges, partly to the fact that some of them do not reach the end of the tube. In some species, as Hemiarcyria rubiformis, the back of the ridge is beset with spike-like processes. Trichia chry- sosperma has a number of smaller slender ridges running between the spiral ridges and parallel to the longitudinal axis of the tube, and connecting each pair of spiral ridges in a scalariform manner (Fig. 193 ¢c). The tubes of the capillitium lie mixed up together in great numbers and folded many times in the sporangium. If they are dried or their water is extracted by alcohol, they stretch themselves out but never become quite straight; if moisture is restored they acquire still stronger curvatures, and the same phenomena are repeated each time that the moisture is changed. This hygroscopic motility and the spiral ridges recall the elaters of the Hepaticae, and the tubes of Trichia have therefore received the name of eda“ers. Certain species of Trichia and Arcyria, some of which have been already named, have the cavity of the stalk of the sporangium filled with vesicles or cells, which resemble spores but are larger and incapable of germination, They may very well be receptacles of excreta like the calcium carbonate-vesicles of the Calcareae. The sporangia of Stemonitis, Comatricha, Enerthenema, and their allies are also distinguished in the mature state by certain peculiarities. ‘They are borne on the stalk described above as being of the thickness of a hair or bristle and narrowing gradually upwards; this stalk passes through the base of the sporangium and occupies its longitudinal axis“as a central column (columella), and either reaches the apex where it expands in Enerthenema into a membranous disk passing into the wall, or comes to an end below the apex and splits as it were into threads of the capillitium. Stalk and columella are hollow tubes, the cavity of which contains air and lumps of some organic substance. The wall is thick and marked with longitudinal wrinkles, and is coloured a dark brown throughout or has an outer layer colourless. The base of, the stalk expands into an irregular membranous disk which rests on the substratum (Fig. 186), The primary branches of the dark-brown capillitium spring with a broad base from the whole outer surface of the columella, or as in Enerthenema only from the disk-like expansion at its extremity. These branches ramify repeatedly in every direction, and the ramifications become united into.a net-work which has everywhere a large number of meshes, A large number of slender branches run from the meshes of the circumference only, and become attached by their free extremities to the wall of the sporangium, The structure of the stronger branches of the capillitium is like that of the columella, but their lumen is not in communication with the lumen of the a ————— =. eS . CH.VIII.—MORPHOLOGY AND COURSE OF DEVELOPMENT.—-MYXOMYCETES, 439 columella; the slenderer branches resemble those of Didymium and Diachea. The wall of the sporangium is a simple and usually very delicate membrane, and liké all other parts is free from deposits of calcium carbonate, The capillitia which have now been described, though of many and apparently very different kinds, must nevertheless from the data before us be all regarded as - peculiar membranous or parietal formations secreted or excreted from the protoplasm. Their material composition is not accurately known and will be briefly noticed again in the sequel, but it would appear to be not essentially different from that of the thicker portions of the outer wall of the sporangium to which they are sometimes attached. In the Calcareae (Physarum, Didymium, &c.) their substance or wall passes continuously into the wall of the sporangium of which they appear simply as processes, and thus closely resemble the branching bands of cellulose which spring from the outer wall of a cell of Canlerpa and stretch into the interior of the cell. That they are at the same time quite or partially hollow and take up excreted matter into their’ cavity, especially into the calcium carbonate-vesicles before described, is in favour of this conception. The wall-processes accordingly serve partly as supports partly as receptacles of the excreta. All that is known of their development (see page 431) is likewise in harmony with this view, which finds important support in Strasburger’s recent observation that the development of the capillitium is essentially the same in Trichia as in the Physareae, though the tubes in the latter lie free and with a blind termination in the spore-plasm or between the spores, and are so like some vegetable cells that they were long taken for cells. According to Strasburger the tubes of the capillitium of Trichia fallax are formed by secretion of a membrane from the round spaces in the protoplasm which are of the same shape as the tubes, and are filled with a fluid (?) and have no nucleus. This would not prevent their also serving as receptacles of any excreta. What is true of Trichia may certainly be assumed of Arcyria and the species allied to it. The exceptional features in the Stemoniteae require therefore no further discussion, 2. The structure of the aethalium in the mature state has been sufficiently explained in the description of the history of the development of the most common form Fuligo varians, the Aethalium septicum of authors, which will be found on page 431. The body, which has the shape of a cake or cushion, is covered with a brittle rind some millimeters in thickness, which is at first of a golden yellow colour but afterwards becomes pale or cinnamon-coloured, and is continued all round the margin into a membranous expansion lying on the substratum. This rind consists of portions of the combined plasmodia which have collapsed and retain only the calcium carbonate and pigment; within it is a dark-gray mass finely speckled with yellow and readily crumbling to powder, and formed of a fine net-work of tubes, which may be nearly 1 mm, in thickness and which have exactly the same structure as the capillitium of the sporangium of Physarum. Other aethalia are connected by their structure with Didymium, Diachea, . Licea, &c., as Fuligo is with Physarum; but some like Reticularia umbrina require further examination. The round sessile aethalia of Lycogala epidendron, Fr., which are as large as a pea or hazel-nut, have a very peculiar structure. ‘They resemble small sporophores of the Lycoperdaceae. Their surface is covered by a paper-like membrane or rind 440 ~ “SECOND PART.—MYCETOZOA.~ ~ (peridium), the outer side of which is irregularly warted, while numerous tangled threads, a capillitium, stretch from its inner surface into the cavity of the body which’ is filled with spores. ‘The rind is composed of two portions having a layer of finely> granular mucilage between them and separating readily from each other. The inner portion in the surface-view is perfectly homogeneous or finely punctated; seen’ in section it is an evidently stratified membrane about 8 p» in thickness and of a bright brown colour. The outer and much thicker portion on the other hand is formed chiefly of a weft of cylindrical tubular branched threads disposed in several irregular layers; the thickness of the threads is usually 20-33 p», and their walls are stratified and thick, sometimes ro » in thickness, the outer lamellae consisting of a homogeneous jelly while the innermost layer is of firmer consistence and provided with slit-like pits or reticulate thickenings. Numerous branches of these rind-threads bend inwards, - and piercing through the inner rind appear as threads of the capillitium in the central cavity. Here they have only the innermost lamellae of their membrane which is pitted or thickened in a reticulate or sometimes annular manner, the outer lamellae coming to an end in the inner rind. The thickenings project outwardly in the form of ridges which have the appearance of wrinkles and vary in height and breadth, being often very flat. The threads of the capillitium, which are often compressed and riband-like, branch and anastomose copiously. Finally the warts on the outer surface of the rind are thick-walled closed vesicles filled with a densely granular substance. ‘These vesicles are undoubtedly remains of plasmodia filled with excreted substances, the whole body having been composed when young of their dense and uniform reticulum. The threads of the outer rind appear to be the thickened and subsequently emptied membranes of other peripheral plasmodial strands; the develop- ment of the inner part is imperfectly known. The space not occupied by the capillitium is entirely filled with spores in all the sporangia of the Myxomycetes. All parts are kept moist with water till they are mature; then the water evaporates, and the wall of the sporangium dries up and opens in various ways to release the spores. The mode of dehiscence is generally very irregular ; the wall as it dries becomes brittle and breaks up into small pieces at the least touch or quite of iis own accord. This is the case in almost all the Physareae, and in Fuligo, Spumaria, Stemonitis and others. In the Cribrarieae the portions of the membrane which have not been thickened fall to pieces, the thickened portions remaining as a delicate lattice work. The rind in Lycogala and Reticularia tears. irregularly and perhaps spontaneously at the apex. In Chondrioderma floriforme the outer layer of the wall of the sporangium splits from the apex into stellately diverging - lobes, In Trichia, Hemiarcyria and Arcyria the dehiscence and the extrusion of the spores is assisted by the expansion of the capillitium caused by desiccation, and in the first genus by the hygroscopic movements also, The wall either opens spon- taneously by an annular fissure in the Jowest part of the sporangium, as in Arcyria punicea and A, cinerea, or in the upper part as in Hemiarcyria rubiformis, or by irregular fissures (Fig. 192 a, 6) either spontaneously or when subjected to a slight amount of violence, The various monographs must be consulted for further details. The ripe spores vary in size in the different species, their diameter being about 5 » in Lycogala epidendron and 15 » in Trichia chrysosperma. In many species single abnormally large spores-often occur amongst the typical ones. They are ee ee eae Fe ped Na! ae ten SS Ue CH, VIII.—MORPHOLOGY AND COURSE OF DEVELOPMENT, —ACRASIEAE, 441 always roundish in form when saturated with water, but as they dry they often become concave or boat-shaped, like the spores of many Fungi (see page 106). They are: provided with an episporium, a thick unstratified membrane which in a few cases, as: in Trichia fallax and some species of Didymium, is two-layered, and is provided in many species with a thinner spot which is perforated in germination and may there-. fore be termed a broad germ-pore. ‘The outer surface of the membrane is smooth or furnished with projections of definite shape (Figs. 192, 193) according to the species and genus, and is usually of a deep colour, being violet or violet-brown for instance: in all Calcareae and Stemoniteae, and yellow and red in the Trichiaceae. The pro- toplasm enclosed by the episporium has been already described. As regards the material composition of the membrane in sporangia, capillitium and spores, we know that it behaves towards reagents in a szmzlar manner to cuticularised plant-cell-membranes and to spore-membranes in the Fungi, but analyses of it are still wanting. The blue or violet colour of cellulose with iodine does not usually appear; but Wigand and myself found exceptions to this rule in Trichia furcata, Wigd., T. pyriformis and T. varia, in which the innermost - layers of the walls of young sporangia become a dirty blue with iodine and sulphuric. acid ; the membranes also of the spores and of the cells which fill the stalk of Arcyria cinerea, A. punicea and A. nutans and those of the spores of Lycogala epidendron all turn a beautiful blue with the same reagents. Further details will be found in the special treatises which will be named below. — In the foregoing account of the Myxomycetes the nomenclature which Rostafinski ‘introduced in his monograph has been substituted for the older, nomenclature, or unequivocal synonyms only of Rostafinski’s. names have been retained. The most frequently recurring names are: Calcareae = Physareae of my earlier works. | Fuligo varians = Aethalium septicum of former authors. Perichaena liceoides = Licea pannorum, Cienk. Chrondrioderma difforme = Didymium Libertianum, Fres.,the ‘ Physarum album’ of Cienkowski. - Licea flexuosa = Licea serpula, Fr., &c, . Further details respecting the nomenclature and the structure of the spore- receptacles should be sought in Rostafinski’s writings: see also Just’s Jahresbericht, for 1873. Seat ACRASIEAE. Section CXXIII: The Acrasieae, which live on the excrements of animals and on decaying parts of plants, commence their development like the Myxomycetes with the escape of a swarm-cell from a spore. The swarm-cell always remains in the form which has amoeboid creeping movements, never assuming that which has cilia and the hopping movement. After multiplying greatly by successive bipartitions the swarm-cells unite again, many hundreds in number oftentimes if the development has been vigorous, in order to form spores. But they do not for this purpose coalesce into plasmodia. ‘The swarm-cells are piled up one on another without coalescing, remaining distinct and artificially separable from one another though closely crowded together, and forming bodies of definite shape which rise perpendicularly above the surface of the substratum, and in which every one or the majority of the swarm-cells assumes the structure of a spore of a Myxomycete, having usually a delicate membrane . 442 SECOND PART.—MYCETOZOA. and being of the average size of from 5 to 10 ». These spore-heaps resemble small sporangia of a Myxomycete, but have no distinct wall; the spores are only held together and surrounded by a slight structureless enveloping substance. Inthe Guttulinae, which have been carefully examined by Cienkowski and Fayod, the development, apart from the possible resting-states which will be described below, ' is limited to the above phenomena. The ripe spore-heaps are formed only of spores. They lie on the substratum as round or elongated bodies of the size of a pin’s head and with the appearance of small white, yellow or red drops. In the other genera of the group Dictyostelium and Acrasis a division of labour appears among the heaped up swarm-cells. When the body which is formed by them begins to rise above the substratum, those which are in its central line form firm outer membranes at the expense of their protoplasm, and are gradually changed into chambers formed of cellulose and filled with a transparent substance. They remain in close union with one another without interstices, and being built up on or against one another in a single row or in several rows in large Dictyostelia, they form a stalk which rests on the substratum and traverses the middle of the body somewhat in the manner of the stalk in the sporangium of Stemonitis (Fig. 186). This stalk grows for a time acropetally by addition of new elements. The aggregate of swarm-cells surrounding the stalk lengthens in proportion as the stalk grows and becomes.corre- spondingly narrower, and ultimately separates from the substratum as the stalk ceases to grow; it then creeps up the stalk leaving it bare and proceeds to form its spores at the apex. This process also is to some extent illustrated by Fig. 186 which represents Stemonitis. In Digtyostelium the spore-masses borne on the stalk resemble in the main those of the Guttulineae. According to Van Tieghem the spores are arranged in Acrasis in rows one above another like beads in a rosary. For further details the reader is referred to Van Tieghem’s and Brefeld’s publications. In Guttulina protea, Fayod found that the swarm-spores grown in a fluid and remaining isolated may undergo the change into spores of the form and structure which they have normally in the state of aggregation. When the conditions are unfavourable for the development these swarm-cells form a thick outer membrane in a complicated manner, and pass into a state which corresponds to the encystment of the swarm-cells of the Myxomycetes (page 427) and may therefore be termed a transitory resting-state. Van Tieghem observed a different mode of encysting in Acrasis and Dictyostelium when the conditions were unfavourable ; a swarm-cell put out a number of processes or arms one after another, which separate from the parent-cell, round themselves off and become invested with a membrane. In Brefeld’s first work on Dictyostelium the development was to some extent incorrectly described, the dense aggregations of swarm-cells which develope into the stalked spore-masses being supposed to be plasmodia, that is, products of the coalescence of swarm-cells, and the rest of the phenomena being interpreted in ac- dance with that supposition. Van Tieghem’s correction of this mistake in 1880 was cautious but at the same time clear and complete, and Brefeld has recently (1884) published a full confirmation of this correction. AFFINITIES OF THE MyceTozoa. Section CXXIV. In investigating the affinities and homologies of the Mycetozoa which have now been described, we must distinguish between the Myxomycetes which — ee CH. VIII.— MORPHOLOGY AND COURSE OF DEVELOPMENT.—AFFINITIES. 443 form plasmodia by coalescence of swarm-cells and the Acrasieae which do not form plasmodia. ‘The two groups are evidently closely related to one another, the only important difference between them being the coalescence of swarm-cells in the one group and their firm aggregation only in the other. It is easy to conceive that the one form of development has proceeded directly from the other, either the Myxomycete form from that of the evidently more simply Acrasieae, or in the converse order. The group of the Mycetozoa differs distinctly from the Fungi which have been the subject. of the first part of this book in all such characteristics as do not belong to all organisms alike, and the descriptions already given of both kinds of plants. render any further explanation of the point unnecessary; their connection also with other known plants is still more remote. The difference would not be less decided, if the Mycetozoa were without their remarkable amoeboid movements, for such movements are observed in other vegetable cells which have not a firm membrane: The characteristic mark of separation lies in the formation of plasmodia or aggregation of swarm-cells, , It is obvious moreover according to our present knowledge that the Mycetozoa are the superior terminal member or the two terminal members of a series of forms or developments which commence elsewhere. The most highly differentiated sections of the group, the Calcareae, Trichiae, Lycogala and others, give evidence of no close affinity with: any more highly differentiated group ; in other words, like the Gastro- mycetes with which they were classed by earlier botanists, they do not connect with any group above them. Hence in enquiring after their affinities we must be content with searching for a possible connection with an inferior group, and for the simpler forms from which they have proceeded. When we seek for such a connection among the forms with which we are acquainted, we find it impossible to establish any strict homologies, and we are limited to the observation of resemblances in form, structure and mode of life. Sucha course of unprejudiced comparison leads us by a very short step to the naked ‘ Amoebae”’ of the zoologists, especially in Biitschli’s sense’, as the starting point,— organisms with bodies having the amoeboid movements of the swarm-cells of the Myxomycetes, which multiply, as far as we at present know, by successive: bipartitions without forming plasmodia, and which may pass singly and without aggregation or coalescence into states of rest not essentially different in their characteristics from those of the spores of the Myxomycetes. Guttulina is really a naked Amoeba of this kind, and is distinguished from other known forms only by the aggregation of its spores. Guttulina protea, mentioned above as forming solitary spores, differs in this respect from the Amoebae ; it may be classed as well with the naked Amoebae as with the Acrasieae, and forms therefore a perfect connecting link with the Amoebae. Thus on the one hand the more highly differentiated Acrasieae join on at once to Guttulina, and on the other a short step further brings us to the type of Myxomycetes which form plasmodia, in which coalescence of swarm-cellsinto a plasmodium and redivision of the plasmodium into spores take the place of their aggregation: Forms like Guttulina may have developed phylogenetically in two divergent directions, on the one hand into the more 1 Bronn’s Thierreich, see below, page 454. 444 SECOND PART.—MYCETOZOA, - highly differentiated Acrasieae, on the other into forms which produce plasmodia. Plasmodiophora, which will be further noticed below, is perhaps one of the simplest representatives of the latter kind, though this must remain uncertain for reasons which will be stated. In the group of the Myxomycetes the type becomes. highly differentiated. From these naked Amoebae with which the Mycetozoa are connected in the ascending line; the zoologists with reason derive the copiously and highly developed section of the shell-forming ‘Rhizopods,’ as they are understood by Fr. E. Schulze and Biitschli, though the course of their ontogenetic development is still imperfectly known. And since there are sufficient grounds for placing the Rhizopods outside the vegetable and in the animal kingdom, and this is undoubtedly the true position for the Amoebae which are their simpler and earlier forms, the Mycetozoa which may be directly derived from the same stem are at least brought very near to the domain of zoology. It has been already pointed out that the Mycetozoa show only a slight agreement, either in the general course of their development or in the characteristic features of its separate stages, with organisms which are of undoubted vegetable origin, whether they be Fungi or plants other than Fungi; the agreement, with the exception of the few cases in which cellulose makes its appearance, is confined to phenomena which are common to all organised bodies. It is exactly in the species, which like Lycogala and Fuligo are most like the Fungi, that the agreement is of the smallest possible amount, being confined to purely external marks such as those between birds and winged insects. On these various grounds, which have been worked out at different times with greater or less clearness according to the state of our knowledge, I have since the year 1858 placed the Myxomycetes under the name of Mycetozoa outside the limits of the vegetable kingdom, and I still consider this to be their true position. We may further enquire whether closer ties of relationship do not appear at some point or other between the group of the Mycetozoa at their lower limits and members of the vegetable kingdom. In the search for these and judging by known facts, we find that the only forms which we can take into consideration are the Chytridieae which have no mycelium, as Synchitrium, Olpidiopsis, Rozella and Woronina (see sections L—LII). ‘It has been already more or less distinctly stated that these forms are nearly related to the Mycetozoa. They agree with the Myxomycetes, first in the peculiar circumstance that the entire vegetative body is finally transformed into one many-spored sporangium, secondly in the fact that their spores and the vegetative body itself in the young state have the power of amoeboid movement for a longer or shorter time. But these are phenomena which are common to them and many other Thallophytes, with which no one ever has supposed or ever will suppose them to have any near affinity, Botrydium for example or Porphyra ; it is plain also that they have been appealed to from a wish to find some group of undoubtedly vegetable forms in which the Myxomycetes could be included. Of the characteristic phenomena of development in the Mycetozoa, the Chytridieze mentioned above show nevther the aggregation of the Acrasteae, nor. the formation of plasmodia by coalescence of swarm- cells, If the term. plasmodium has in their case been used to describe bodies originating in the growth of a single spore, this arose either from an erroneous idea (Cornu), or it is a misuse of the word, for though Chytridium in its young state often CH, VIII.—MORPHOLOGY AND’ COURSE OF DEVELOPMENT.—AFFINITIES. 445 shows the amoeboid movement of a plasmodium, it has not the character which is involved in the origin of a plasmodium; this is the case too with the spore * of Porphyra which also has the power of amoeboid motion. There is therefore no real ground for assuming a direct relationship with these Chytridieae, whether they do or do not form a natural group with the other species which produce mycelia, a question which, as was explained in Chap. V, must for the present remain undetermined. It is a totally different question whether it is possible to suppose a common origin for these particular Chytridieae and the Mycetozoa, and consequently a more remote and indirect relationship. ‘The comparison of the facts known to us shows it to be probable, as Biitschli points out, that the starting point of the naked Amoebae of the zoologists is to be sought in the group of very simple organisms known as the Flagellatae, and a study of the swarm-spores of the Mycetozoa leads to the same view, for in the stage of their existence when they are furnished with cilia they have all the characters of the simpler Flagellatae. But not only the Chytridieae which produce no mycelium but all the group show such close affinity to the Flagellatae, that they might if necessary be phylogenetically derived from them. But this is true also of the entire assemblage of the simple Algae, with which it was sought to connect the Fungi in the sections of Chapter V. We may as well place the Volvocineae ‘with the Flagellatae as with the Chlorophyceae, if we prefer. that arrangement, and no one will doubt the close affinity which exists between them and the rest of the undoubted Chlorophyceae. If then we distinctly separate the Mynelodots from the Fungi, and are prepared even to draw the boundary line which divides the two organic kingdomsbetween these groups, we do not thereby deny that members of the two divisions may approach very near to the group of the Flagellatae, towards which all the evidence shows that the two kingdoms converge, and thereby approach also very near to one another. The purpose of the foregoing remarks has been to do for the Mycetozoa what was previously done for the Fungi, namely to establish their affinities on the foundation of the facts of which we are at present in possession, or speaking more boldly to give the true account of them. Such an attempt whenever made must be made with the material then at hand. If the foundation of facts changes with the progress of our researches a fresh attempt must be made. The views of botanists as to the position of the Mycetozoa in the system, have already varied much in the course of time. The older view just noticed above, which placed the Myxomycetes with the Gastromycetes on the strength of a mere resem- blance between the mature sporangia in the two groups, has now only a historical interest. Further remarks on this point will be found in my monograph of 1864. The ideas with regard to the place of the Mycetozoa in the natural system which were expressed by Famintzin and Woronin in their beautiful work on Ceratium do not at the present day call for discussion. Cornu in 1872 endeavoured to connect them - with the Chytridieae, chiefly by assuming the formation of plasmodia in the genera of Chytridieae which do not produce a mycelium; but we have already shown that this assumption is without foundation. The opinion represented in Brefeld’s work on Dictyostelium (page 20), that this organism might connect the group of the Myxomycetes with the Fungi through the Mucorini, is refuted by a comparison of the course of development in the two groups. The more recent utterances of the same writer on the . 446 SECOND PART.~—MYCETOZOA, point under consideration presuppose on the one hand their connection with the Fungi as something ascertained, and on the other hand in dealing with the affinities of the Fungi so leaves the firm ground of definite facts for the regions of speculation, that they cannot be admitted into a discussion which keeps close to facts. The view lately promulgated by J. Klein in his treatise on Vampyrella is essentially the same as that which would derive the Myxomycetes and the Chytridieae from a common stein lying outside the series of Fungi. It sees the form, from which Myxomycetes, Chy- tridieae and Rhizopods all descended, in the Vampyrellae which belong either to the Rhizopod-type (or Heliozoa-type) or to that of the Myxomycetes, but it can hardly be said to have any foundation in facts; it should have gone somewhat further back to the Flagellatae, as has been suggested above. DOUBTFUL MYCETOZOA. Section CXXV. I here exclude from the ranks of the true Mycetozoa a few forms or groups of forms, some of which have been occasionally mentioned in the preceding sections, These forms so far as they are known have many points of resemblance with the Mycetozoa, but either our knowledge of them is imperfect, or else they depart so far in certain points from the typical Myxomycetes and Acrasieae, that it is better to have their position in the system for the present undetermined, At the same time we may properly give a brief enumeration and description of them in this place. Bursulla crystallina, Sorokin, is, according to the author’s account of it, a very small Myxomycete growing on horses’ dung, with an ovoid stalked sporangium 0.03 mm. in height, and forming eight spores by simultaneous division. The spores before they become invested with a firm membrane escape from the swollen apex of the sporangium in the form of swarm-cells without cilia but capable of amoeboid move- ment, and subsequently coalesce in indefinite numbers and form plasmodia, which in their turn become fashioned each into a single sporangium or into a group of several sporangia according to their size. Sorokin saw no nucleus in the swarm-cells at the ordinary vegetative temperature ; on the other hand a nucleus was observed when the sporangia were exposed to a very low temperature (as low as —27°C). The develop- ment was in other respects the same; we may conclude therefore that the nuclei of the swarm-cells had been overlooked in the first-mentioned case. We may venture therefore a step further and assume that when a swarm-cell with a nucleus encounters one which is supposed to be without a nucleus, the two coalesce into a cell which forms a membrane and passes into a resting state as a kind of oospore; and that after hibernation the protoplasm issues forth from the membrane and becomes fashioned into an ordinary sporangium. This may in fact be simply a case of the encystment of small plasmodia, Apart from the peculiar features which require examination we may really have a small Myxomycete before us in Bursulla. The course of development in Haeckel’s pelagic Protomyxa aurantiaca entirely resembles that of a Myxomycete. ‘Protoplasmic body, a plasmodium of an orange-red colour, (always?) formed by coalescence of several swarm-spores, 0.5-I mm. in diameter; with very many thick arborescently branched pseudopodia which form a net-work by frequent anastomoses. Resting state, a spherical lepocytode with a diameter of 0.15 mm., and a thick structureless envelope (cyst). Swarm-spores CHAPTER VIII.—MORPHOLOGY AND COURSE OF DEVELOPMENT. 447 pear-shaped, conical at the smaller end and running out into a very strong flagellum ; movement that of the swarm-cells of the Myxomycetes. ‘The spores when they come to rest creep about in the manner of the Amoebae.’ Such is Haeckel’s diagnosis. This organism differs from the Myxomycetes chiefly in the absence of firm spore- membrane, and in the circumstance that neither ¢ell-nucleus nor division of the swarm- cells has been observed. Myxastrum radians, Haeckel, also a marine form and dis- tinguished by the presence of silica in the spore-membranes, appears to be nearly allied to Protomyxa. Cienkowski’s Vampyrellae are organisms with amoeboid movement which live on Algae and Diatoms. Some like Vampyrella Spirogyrae and V. pendula suck the pro- toplasm and chylorophyll-corpuscles from out of the living cells of species of Spirogyra or Oedogonium, when they have pierced their walls, while V. vorax embraces the entire cells of Diatoms, Desmids and similar forms with their pseudopodia, and absorbs them into its own substance. In both cases the reception of a certain quantity of food is followed by a period of rest, a smoothing of the surface of the body and the excretion of a delicate firm membrane. In this state of rest the bodies which have been absorbed are digested, that is are dissolved till there remain only comparatively minute portions of the protoplasm which have assumed a brown colour, and in the case of Vampyrella vorax of the membranes. Next follows the excretion of the undigested substance from the living protoplasm, the division of the latter into usually 2-4 swarm- cells and their escape from the membrane; the two processes go on simultaneously, the division being effected while the spores are escaping at 2-4 separate points. Then according to J. Klein from 2-4 swarm-cells, seldom more, at once coalesce again and form a. plasmodium, which repeats the process just described of absorption of food and subsequent formation of swarm-cells, In addition to this course of develop- ment resting cysts may also be formed, in which case the body which has come to rest inside the membrane excretes undigested remains of the food, and then without forming swarm-cells excretes a new membrane. The subsequent fate of these cysts is still unknown, Other transitory states of rest, as in the small cysts of the Myxomycetes, may occur within the periodic course of development described above, and no coalescence may take place, the cells passing singly through the swarming state as aboye but not forming plasmodia. Cienkowski’s Nucleariae appear to be just like the Vampyrellae in the course of their development and in their manner of life. They are distinguished from them by the presence of nuclei, which are said to be wanting in the Vampy- rellae. Coalescence into plasmodia has not been observed in them, but it is not excluded by the ascertained facts. Cienkowski’s Monas Amyli has motile swarm-cells provided with two cilia, and a number of these cells surrounding a starch-grain may coalesce into small plasmodia. The plasmodium forms a membrane, and after its substance has increased in size at the expense of the starch-grain it produces a large number of new swarm- cells by simultaneous division. It is said also that a single swarm-cell may spread itself round a grain of starch without uniting with others to form a plasmodium, and thus become the starting-point of the development which was described above. An exactly similar course of development has been observed in Klein’s Monadopsis and Cienkowski’s Pseudospora and Colpodella, except that the latter 448 2 SECOND PART.-—MYCETOZOA, two genera, as far as is at present known, do not form plasmodia, but each swarm-cell after absorbing food becomes the mother-cell of a new generation of swarm-cells. Plasmodiophora Brassicae is parasitic on the roots of cruciferous plants, especially species of cabbage, and causes large swellings on them. An amoeboid swarm-cell with cilia escapes from the round thin-walled spore in water, and pene- trates without first undergoing division into the epidermis of the young root and from thence into the parenchymatous tissue. Then the cells of the host become greatly enlarged and large bodies with amoeboid movements make their appearance in them ; but it could not be certainly determined whether these bodies were due to the growth of one swarm-cell, or to the coalescence of several swarm-cells as in the Myxomycetes, or possibly to a modification of the protoplasm similar to that which occurs in Rozella (see page 395). Ultimately the entire protoplasm contained in a cell of the parenchyma becomes motionless and divides simultaneously into a very large number of spores of the character stated above, and in this case also without previously forming a special membrane. Finally Zopf! appears to include all sorts of lower organisms with amoeboid movements together with some of the forms last described under the name of ‘lower slime-Fungi.’ This use of the term does certainly not correspond with the meaning hitherto assigned to it, and to avoid any misunderstanding I say very distinctly that this application of the term and therefore also the discussion of any other forms than those which have now been mentioned cannot be admitted in this place. CHAPTER IX. MODE OF LIFE OF THE MYCETOZOA. _ Section CXXVI. Germination. The spores of the Mycetozoa, in which the germination has been observed, are able to germinate from the moment that they are ripe. Some retain the power of germination for a long time if protected from injury ; many Calcareae, for example, Physarum, Didymium, Chondrioderma, Peri- chaena liceoides, retain their vitality 2-3 years, some, as Physarum macrocarpum according to Hoffmann, eve for 4 years. In Trichia varia and T. rubiformis vitality lasted according to express observations only 7 months; in other species of Trichia and allied forms it appears to be extinguished at a still earlier period. The requisite conditions for germination in most known forms are the usual spring and summer temperature of our temperate climates and a sufficient supply of water. The majority germinate readily when placed in pure water, well developed fresh material often in a few hours. Nutrient substances dissolved in the water do not hinder germination; this at least was found to be the case in Fuligo and Chondrioderma. The Ceratieae and such Acrasieae as have been examined do not germinate in pure water, but only in a suitable nutrient solution. The like necessity and the use of unsuitable solutions may account for the want of success which has attended the attempts hitherto made to procure the germination of their spores of the Cribrarieae and Tubulina. See Biolog. Centralblatt, Bd. III, Nr. 22. CHAPTER IX.—MODE OF LIFE OF THE MYCETOZOA. 449 The requisites for germination are the same in sclerotia and cysts as in spores, as was stated above on page 428, where also will be found all that is known of the external causes which lead to the formation of these states. Section CXXVII. Some account has necessarily been already given in section CXIX of the phenomena attending the life of the plasmodia. For many general questions which here come under consideration, the reader is referred, in ac- cordance with the purpose of this book, to works on general physiology, and especially to Pfeffer’s Physiology, vol. II, chap. 8 and Stahl’s latest publication on the subject, and the account here given must be confined to a short review of their mode of life. This has been, investigated chiefly in the plasmodia of the Physareae, Fuligo especially, which are readily procured. What is known of other forms appears to agree with the accounts given of the Physareae, but requires more exact investigation, Movement of plasmodia. The internal causes of the changes of shape, of the protrusion and withdrawal of processes and the interior streaming of granules, which are attendant on the organisation of the protoplasmic body. and are to a great extent unknown to us, cannot of course be discussed in this place. The most important external causes of the movements of the plasmodium and of the changes in its form are, the z//umination, the distribution and movement of the water in the substratum, the chemical nature of the environment, and the conditions of temperqture. It is uncertain to what extent purely mechanical influences are also operative. Rosanoff’s former assumption of geotropic movements has proved to be without foundation. We may therefore, in accordance more or less with the general terminology of the movements of growth, speak of phenomena of Aeliofropism, hydrotropism and rheotropism, trophotropism and thermotropism. Heliotropism. A vegetating plasmodium stretches out its branches: and reticulations uniformly in every direction on uniformly moistened surfaces, such as paper steeped in water and kept in a dark or equably but faintly illuminated chamber. If the intensity of the illumination is increased, the power of movement, according to Baranetzki, is generally diminished, and if the amount of illumination is different in different portions of the expanded surface, the branches are drawn in from the bright side and others are put forth towards the darker side; the plasmodium also moves towards the darker side. The direction of these movements is independent of the direction of the beams of light which fall on the plasmodium, being determined only .. by the intensity of the illumination. Hydrotropism. If while all other conditions are uniformly favourable the water is unequally distributed in the substratum, the vegetating plasmodia, if not on the point of forming spores, withdraw from the drier spots when the dryness has reached a certain degree and wander towards the moister. Rheotropism. If a stream of water is made to flow slowly through a moistened porous substratum, such as filtering paper or strips of linen cloth, the plasmodia which are vegetating on the moist surface wander in the direction of the stream, without regard to the particular direction in space in which it moves. Trophotropism. Vegetating plasmodia spread out on surfaces which yield little or no nutriment move towards bodies which contain nutrient substances as [4] Gg 450° SECOND PART,—MYCETOZOA, soon as they are offered to them, here too without regard to the direction in space in which the movement has to be made. If the plasmodium of Fuligo which usually lives in tan is spread out on the moist vertical wall of a glass, it remains in this position, other things being the same, as long as the surface of the glass is covered with a film of pure water. If an infusion of tan is added to the water, in such a way that the plasmodium is touched by it at one spot only, it begins to move rapidly towards this spot and gradually puts out numerous branches which dip into the infusion. A small piece of tan placed close to a plasmodium under similar conditions is quickly seized by a number of freshly protruded branches. The similarity in the effect of the fluid containing the infusion of tan and the solid piece of tan shows that it can only be due to chemical constituents of the tan; what these are has not been precisely ascertained. If a plasmodium comes into contact on one side with other bodies dissolved in water, the opposite effect is produced, namely repulsion of the plasmodia. Even a solution containing 4 or } per cent. of grape sugar produced this effect at first in Stahl’s experiments, but the plasmodium by degrees became accustomed to it and behaved to it as to the infusion of tan. A sudden change in the concentration of the saccharine solution, either by increasing it to a certain amount (2 per cent.) or diminishing it, gives rise to similar phenomena to those first described. Stahl observed the same repulsions in experiments with saline solutions. If oxygen is excluded on one side, a movement takes place, as might have been expected beforehand, towards the side where oxygen is admitted. Thermotropism. If the substratum, other conditions being the same, is unequally warmed on different sides, the plasmodium moves, at least within the limits of temperature observed in Stahl’s experiments (+ 7° to 30° C.), towards the side which is most highly warmed. Most of the phenomena observed in spontaneously vegetating plasmodia, especially their creeping hither and thither and in and out, according to the time of the year and the state of the weather, on the substratum of vegetable remains, such as leaves, tan and the like, may be explained very simply from the experimental results here recorded. A further fact established by Stahl must be added here in explanation of another and very remarkable phenomenon, namely that in the plasmodia of Fuligo and some species of Physarum, in which the point could be examined, the reaction against locally unequal distribution of water in the environment changes with the age. The plasmodia are positively hydrotropic, that is wander from the dry to the moister spots, other things being equal, during the vegetative stage, but become megatively hydrotropic near the moment of formation of sporangia, that is they move from the moister to the drier spots. This movement also takes place without regard to the mere direction in space, and so may be upwards or downwards &c., and it explains the general fact that almost all plasmodia, as soon as they are ripe for forming sporangia; move to comparatively very dry spots on the surface of the moist substratum, often travelling a considerable distance, before being transformed into sporangia; it explains also, according to Stahl’s observations, the elevation of the commencing sporangium in a direction at right angles to the comparatively moist substratum. a ee —- eee CHAPTER IX,—MODE OF LIFE OF THE MYCETOZOA. 451 Further investigation is necessary to determine whether other causes also may not assist in certain cases to give rise to the latter phenomenon ; the question also, whether the peculiar characters of plasmodia under discussion may not change at a certain period of their development in relation to other things, as well as to hydrotropism, has still to be examined, especially with reference to a statement of Hofmeister’ that certain plasmodia moved towards the side of strongest illumination. To the movements which have now been described must be added one more which requires a brief consideration. It was stated above on page 425 that small solid bodies are engulphed in the substance of the plasmodia, at least in the Cal- careae’ or Physareae. This is effected by definite movements; the surface of the plasmodium rises cushion-like round the bodies which are in contact with it, and the margins of the raised part gradually run together over them and cover them. This phenomenon occurs in the plasmodia, as soon as they have been formed by coalescence of swarm-cells, but not in the swarm-cells themselves, if we put aside certain isolated observations on Dictyostelium which have yet to be confirmed, It is not confined to any particular spot of the plasmodium, and may continue till sporangia begin to be formed; then the foreign bodies which have been absorbed and are still present are all ejected, some of them even at an earlier period. All this shows, that the solid bodies are not simply squeezed into the soft and passive substance of the plasmodium, but that there is a reaction of the plasmodium in response to the stimulus which it experiences from contact with them. Substances of various kinds are taken in this way into the substance of the plasmodium: fragments of dead vegetable cells, spores of Fungi and of the Myxomycetes themselves, sclerotium-cells of Myxomycetes, grains of starch, small portions of colouring matters if brought near the plasmodium. All these substances it should be observed consist of organic compounds, and it is highly probable that some of them at least supply food to the plasmodium which has engulphed them. It is not certainly ascertained whether entirely indifferent inorganic substances are absorbed by it. The question therefore remains unanswered, whether the movements of engulphing are caused by the purely mechanical stimulus of contact, or by certain chemical qualities of the substance to be engulphed. In the latter case the phenomenon would rank immediately with the movement in the direction of nutrient bodies described above, and both would be special cases of a more general law of reaction in response to chemical irritants, An old observation of my own supports the view that the reaction not only is or may be dependent on a definite chemical quality in the body which causes the stimulus, but that plasmodia of different kinds react unequally on the same stimulation. A number of pieces of carmine were absorbed by Didymium Serpula, scarcely any by Chondrio- derma difforme. Section CXXVIII. The process of nutrition takes place only in the amoeboid states of the Mycetozoa, in the swarm-cells therefore and the plasmodia. All the better known Myxomycetes in their actual primary adaptation are saprophytes ; 1 Pflanzenzelle, p. 20. Gg2 452 . SECOND PART.—MYCETOZOA. they live on dead organic and especially vegetable substances, of course with the necessary ash-constituents, and are found therefore chiefly in accumulations of dead parts of plants—leaves, tan, rotten wood, and the like. What definite chemical substance does actually and usually serve or is fitted to serve as nutrient material to the Myxomycetes is a question which has not yet been thoroughly examined. The facts recorded above show that the food is taken in during the swarm-cell condition only in the fluid state or state of solution, and this is also the case, at least in most instances, with the plasmodia, That it is so appears, to say the least, extremely probable by the behaviour of the plasmodia of Fuligo to the extract of tan, as shown by Stahl’s experiments quoted above. This agrees with the observation that plasmodia of Chondrioderma difforme may be obtained from spores in watery infusions of vegetable substances though no solid bodies are supplied to them, and lastly with the fact that solid ingesta have never been found in the plasmodia of certain species, as Lycogala, though it must be allowed that these have not been very thoroughly examined. On the other hand we see solid bodies taken up by the plasmodia which have been more particularly described above, among others by Chondrioderma, and some of them at least again thrown out. The body taken into the plasmodium is often more or less perfectly dissolved. It has already been stated that the sclerotium-cells of a species engulphed by its own plasmodium gradually disappear and pass into the substance of the plasmodium, but it is uncertain whether this is a case of actual dissolution of the body introduced, or of a coalescence with the body which absorbs it, like that of the swarm-cells or the branches of the plasmodium. In the plasmodium of Didymium Serpula which were fed with carmine, the fragments of carmine were to some extent at least dissolved ; they were repeatedly carried along in the stream of granules, and in twenty-four hours’ time were enclosed each in a vacuole filled with a clear red solution. This continued for several days. On the other hand the Chondrioderma mentioned above showed no signs of dissolving the few fragments of carmine which it received into its substance. In. experiments instituted by Dr. Wortmann a number of starch-grains were taken in by plasmodia of Fuligo, and they showed deep corrosions in the course of from two to three days. This shows the presence of a ferment capable of dissolving starch and confirms Kiihne’s previous determination. A ferment which acts upon cellulose must be present, at least during the passage of the sclerotia of Fuligo into the motile condition, because the cellulose membranes are rapidly dissolved during that time. Krukenberg has ascertained the presence of a peptonising ferment’. These facts all point to the conclusion that the solid ingesta are to some extent at least appropriated as food and digested, the undigested remainder being then cast out. We have no exact physiological investigations of these questions and of others which are connected with them. So far as plasmodia devour and digest living bodies, the name of saprophytes can only be applied to them with some modification of its ordinary mean, ; Some of the forms which were classed above as doubtful Myxomycetes, Bursulla for example, are saprophytes in their mode of life. The account given above of * Unters. d. physiol. Instit. z. Heidelberg, II, p. 273. See also Reinke cited on p. 52. CHAPTER IX.—MODE OF LIFE OF THE MYCETOZOA. 453 Plasmodiophora shows that it is, in the terminology employed in the Fungi, an en- dophytic parasite which greatly deforms its host. Vampyrella and the forms with a similar mode of life must no longer be termed parasites; they devour other organisms wholly or partially, absorbing the objects which they admit into their sub- stance by the same or nearly the same movements as those by which plasmodia take in their solid ingesta. Literature :— E. FRIES, Systema mycologicum, III, 1829. A. DE BARY, Die Mycetozoen (Zeitschrift f. wiss. Zoologie, Bd. X, 1859, and 2nd ed. Leipzig, 1864). For a variety of details and full accounts of the literature of the subjects the student is referred to the second edition of my work and to the ‘llesing publications : L. CIENKOWSKI, Zur Entwicklungsgeschichte der Myxomyceten, and Das Plasmodium in Pringsheim’s Jahrb. f. wiss. Bot. III, 325 and 4oo. J. T. RoSTAFINSKI, Versuch eines Systems der Mycetozoen (Diss. Strassburg, 1873) ;— Id., Slucowce (Mycetozoa), eine Monographie, Paris, 1875 (in Polish), with full lists of works on the subject down to 1875. J. ALEXANDROWITSCH, Ueber Myxomyceten (in Russian), Warsaw, 1872. STRASBURGER, Zur Entwickelungsgeschichte der Trichia fallax (Bot. Zeit. 1884, p. 305). . A, FAMINTZIN u. M. WORONIN, Ueber Ceratium hydnoides u. C. porioides (Mém. Acad. Pétersbourg, XX, No. 3, 1873). O. BREFELD, Dictyostelium mucoroides (Abh. d. Senckenb. Ges. VII, 1869) ;—Id.; Untersuchungen aus der Gesammtgebiete der Mycologie, I, Leipzig, 1884. L. CIENKOWSKI, Ueber einige protoplasmatische Organismen (Guttulina). See Just’s __ Jahresber. for 1873, p. 61. VAN TIEGHEM, Sur quelques. Myxomycétes 4 plasmode agrégé (Bull. Soc. bot. France, 27 (1880), p. 317. V. Fayop in Bot. Ztg. 1883. Guttulina protea. L. CIENKOWSKI, Beitrige zur Kenntniss der Monaden in M. Schultze’s Archiv f. Mikrosk. Anatomie, I, p. 203, tt. XII-XIV. See also Regel in Bot. Ztg. 1856, p. 665. M. WORONIN, Plasmodiophora Brassicae in Pringsheim’s Jahrb. XI, p. 548, tt. 29-34. . E. HAECKEL, Monographie der Moneren (Jenaische Zeitschr. IV, p. 64). F. E. SCHULZE, Rhizopodenstudien (Arch. f. Mikrosk. Anatomie, XI and XIII, p. 9). -* J. KLEIN, Vampyrella (Bot. Ztg. 1882 and Bot. Centralbl. XI (1882), Nr. 5-7). N. SOROKIN, Bursuila crystallina (Ann. d. sc. nat. sér. 6, II, p. 40, t. 8). S. ROSANOFF, De Vinfluence de Il’attraction terrestre sur la direction des Plasmodia des Myxomycétes (Mém. Soc. de Cherbourg, XIV, p. 149). J. BARANETZKI, Influence de la lumiére sur les Plasmodia des Myxomycétes (Mém. Soc. de Cherbourg, XIX, p. 321). E. STRASBURGER, Wirkung des Lichtes und der Warme auf Schwarmsporen. Jena, 1878, p. 69. E. STAHL, Zur Biologie der Myxomyceten (Bot. Ztg. 1884). The zoological material, which lies on the confines of the domain of the Mycetozoa and encroaches upon it, together with a list of works on the subject will be found in the copious treatise of H. G. Bronn entitled Klassen and Ordnungen des Thierreichs, I, Protozoa, edited by O. Biitschli, Leipzig and Heidelberg, 1880. The student is specially referred to this work. Tuirp Part. BACTERIA OR SCHIZOMYCETES. CHAPTER X. MORPHOLOGY OF THE BACTERIA. Section CXXIX. The forms which we have now to consider are termed by Nageli' Schizomycetes or Fission-Fungi; they are known also by an older name, Bacteria, which was restored by Cohn in 1872 as the designation of the entire group. I prefer the latter appellation for a group which not only includes Fungi in Nageli’s sense, namely Thallophytes which have no chlorophyll, but has among its most characteristic members forms which .contain chlorophyll and cannot therefore with any propriety be termed Fungi. I avoid the use of the term Bacterium as a generic name. To denote the species which constitute the genus Bacterium of authors, I use partly the generic name Bacillus which will be more precisely de- fined in the sequel, and partly the name Arthrobacterium, the latter being applied to all species in which endogenous formation of spores, to be described presently, has not yet been observed, It must not be supposed that we have in this way effected a final reform of the nomenclature ; we gain only a short expression for the present state of our still very imperfect knowledge. The Bacteria consist of minute cells often less than 1 in breadth, and are either isodiametric or roundish in shape or else cylindrical and rod-like; they multiply if supplied with a sufficient amount of food by successive bipartitions, each cell dividing into two similar daughter-cells through an unlimited number of genera- tions. The successive divisions are in most cases all in the same direction, and hence all the cells which have proceeded from one initial cell are arranged in a single simple filiform row if they remain united to one another. All the members of the row are alike capable of growth and division. It less frequently happens that, without any other change in the behaviour of the cells, the successive divisions take place in alternately varying directions, so that the arrangement of the generations which continue connected together is from the first other than that of a simple row. Verhandl. d. Deutschen Naturforscher-Versammlung zu Bonn. See Bot. Ztg.'1857, p. 760. CHAPTER X.—-MORPHOLOGY OF THE BACTERIA. 455 Little is known of the more intimate construction of the cells of the Bacteria, owing to their minute size. All that can with any confidence be affirmed of the greater part of them is founded less on direct observation than on the analogy of the larger cells of other organisms, with which they agree in their chief characteristics so far as these can be recognised, and with which they are also connected by inter- mediate forms. The protoplasm of the cell in most forms and even in the larger ones appears, when in a state of active vegetation, to be a homogeneous and faintly refringent mass filling the cell-cavity. Distinct little granules (microsomata), the constitution of which is still undetermined, may be distinguished occasionally in the larger forms in this condition. They appear in greater abundance as the vegetative activity diminishes, and the protoplasm may then be still more frequently seen to form a parietal layer inclosing a pellucid central. cavity. Highly refringent (crystalline) granules of sulphur, which owe their origin to the decomposition of the sulphates by the plant, are often imbedded in considerable quantity in the protoplasm of the species of Beggiatoa which grow in springs containing sulphur, as was first ported out by Cramer and Lothar Meyer. The protoplasm of some species which appear to belong to this group forms chlorophyll, and seems to be coloured green throughout by this substance. Van Tieghem found two forms of this kind living in water, which he distinguishes as Bacterium (Arthrobacterium) viride and Bacillus virens'; W. Engelmann a third marked by the very pale tint of its chlorophyll, which he names Bacterium (Arthrobacterium) chlorinum *, Most species are distinguished by the absence of chlorophyll and analogous colouring-matters. In this respect they agree with the Fungi, and it is owing to this fact and its physiological consequences that they have received the name of Fungi. In some species, Zopf’s Beggiatoa roseo-persicina for example and its subordinate forms, the protoplasm is uniformly tinged with a red colouring-matter, which Lankester has carefully examined and named bacteriopurpurin*. It is not yet certainly ascertained whether the colouring matters, which often give an intensely red, blue, yellow, or other tint to the gelatinous accumulations of some small forms, such as Micrococcus prodigiosus, are contained in the membranes only or are attached also to the protoplasm. Some species which contain no chlorophyll form a substance in their protoplasm, which from its behaviour with reagents and the physiological relationships observed in certain cases, must be considered to be more or less like starch, or more correctly granulose. The cells of Prazmowski’s Bacillus (Clostridium) butyricus (Amylobacter Clostridium, Trécul) and Spirillum amyliferum, van Tieghem*, become more highly refringent in the stages which precede the formation of spores (section CXXX), and their protoplasm then assumes a blue or violet colour with solution of iodine, either 1 Bull. Soc. bot. de France, 27 (1880), p. 174. The figure there given by Van Tieghem from Perty is interesting, but it must remain a question whether it belongs to this group. ? Bot. Ztg. 1882, p. 323. § Quart. Journ. of Micr. Sc., New Series, XIII (1873), p. 408. * See Prazmowski, Unters. ii. d. Entwickgsg. u. Fermentwirk. einiger Bacterienarten, Leipzig, 1880, and Van Tieghem in Bull. Soc. Bot, de France, XX VI (1879), p. 65. 456 THIRD PART.—BACTERIA OR SCHIZOMYCETES. throughout or with the exception of certain transverse zones which do not turn blue ; and in both cases the substance which has become blue spreads uniformly through the protoplasm, without forming bodies in it of definite shape. ‘This phenomenon has been observed when the nutrient substratum contains starch, and when it is entirely free from starch. .The amyloid substance.disappears with the formation of spores. This amyloid reaction with iodine occurs in Hansen’s vinegar-forming Arthrobacterium (Bacterium) Pastorianum, and occasionally in Leptothrix buccalis *, but without proof of any connexion with spore-formation; it is not found in the majority of the forms which have been examined, nor is there any report of the occurrence of amyloid bodies in the species which contain chlorophyll. Nuclei have not as yet been observed in Bacteria. The protoplasm of the Bacteria is surrounded in all cases, so far as we can de- termine, by a membrane. In the case of cells or cell-rows which vegetate actively in a fluid as isolated bodies and do not become cemented together into large masses the cell-wall appears on the lateral faces of the protoplasmic body as a thin bounding surface; on the boundary lines of cylindrical cells closely united in rows it is a-septum; which is in many cases only to be distinguished by the use of desiccating and colouring reagents, and is so entirely invisible in the living specimen that a cell-row composed of several cells looks like a homogeneous unsegmented cylinder. This delicate - membrane immediately clothing the protoplasmic body must, in some forms at least, and especially in some species of Spirillum, be highly extensible and at the same time elastic. The straight cylindrical body in these species is often seen to bend strongly backwards, and then to recover its former direction. According to the views which prevail at the present day it is the protoplasm only that can be supposed to be the active cause in this phenomenon, and the investing membrane must possess the qualities just mentioned to be able to follow its movements. Few or more probably no vegetating cells of Bacteria are clothed with this delicate membrane alone at the highest stage of their development. This is only the inner- most lamella of a membrane which increases in thickness, and in doing so swells and becomes gelatinous in its outer portions. Such gelatinous outer layers or invest- ments are found wherever care is taken to observe them, and direct examination shows that they are either connected in the manner indicated with the delicate inner membrane or are formed from it. The particular character of the gelatinous envelope varies in the dilfeseot species within wide limits. In the freely moving rod-like cells of the typical Bacteria it is invisible, but it can be recognised in the flakes of slimy matter formed by larger accumulations of these forms. In other cases it is of greater thickness and firmer consistence, and may either form distinct gelatinous sheaths round isolated cells and aggregates of cells, or unite and cement the cells together into larger gelatinous masses. The chemical composition of these gelatinous membranes would appear to be very different in different species. Low” found that the membranes of the mother of See Zopf, Spaltpilze. ? Nageli, Ueber d. chem. Gicaimnane Hefe er d. Miinchener Acad., Mai, 1871); —Id., Theorie d. Gahrung, p. 111. dil nh, din lial iin, aii CHAPTER X.—MORPHOLOGY OF THE BACTERIA, 457 vinegar, and Scheibler and Durin’ that those of Leuconostoc mesenterioides, were chiefly composed of the carbohydrate which comes nearest to cellulose; but it appears probable from the researches of Nencki and Schaffer? that in the gelatinous masses (zoogloeae) of purtrefactive Bacteria it consists chiefly of the albuminoid compound which is the principal constituent of the protoplasm of the cell, and to which these writers have given the name of mycoprotein, in combination with infinitesimal quantities of cellulose-like substance. I speak of this as probable only, because it is always a little doubtful how far the substances discovered by macrochemical examination have belonged to the one or the other portion of these minute bodies. The membranes are in very many cases colourless; but in some instances, as has been already said, it is supposed that the intense blue, red, and other hues assumed by some bacteria-masses, and due to colouring-matters resembling anilin dyes, do really belong to the gelatinous membranes, provided they are not excretory products which have found their way into the substratum*, The sheaths round the filament of Cladothrix and Crenothrix are often rust-coloured or dark brown from the > presence of ferrous hydrate disseminated through their substance. Many forms of Bacteria have the free movement of swarm-cells in fluids. Their rapid forward motion is accompanied with rotation round their longitudinal axis, and in many cases with apparent curvature of their bodies. But many observa-. tions under the most favourable circumstances have failed to detect in these forms anything like a distinct organ of locomotion. There are however other swarming forms in which extremely delicate filiform processes described as cilia or ‘flagella’ have been observed since Cohn’s, or even perhaps since Ehrenberg’s time; these processes appear at one or both extremities, one usually but sometimes two or even three together, proceeding from the same point. It would appear to be uncertain whether these formations, like the cilia of other vegetable swarm-cells, are parts and processes of the protoplasm and project through the membrane, or whether they belong to, and are appendages of the membrane itself. The grounds which Van Tieghem * alleges for the latter view, namely that no direct connection can be traced between these processes and the protoplasm of the cell, while they behave towards colouring reagents in the same way as the membrane and not as the protoplasm, are against their being true cilia. It is to say the least questionable whether they function as organs of locomotion, considering the irregularity of their occurrence in the forms which are endowed with motion; and it would also be well to enquire whether the so-called flagella or cilia may not vary in character according to the species, and belong in some instances, as for example in Bacillus subtilis, to the membrane, in others, as in the larger arthrosporous species, to the protoplasm. According to the shapes in which they appear in the vegetative states a series of principal forms are distinguished :-— ? See Van Tieghem in Ann. d. sc. nat. sér. 6, VII, p. 180. ? Journ. f. pract. Chemie, neue Folge, 20 (1879), p. 443. * See Schroter, Ueber einige durch Bacterien gebildete Pigmente, and Cohn’s Beitrage z. Biol., Heft 2, p. 109; also Nageli, Untersuch. ii. niedere Pilze, p. 20. * Bull. Soc, Bot. de France, XX VI (1879), p. 37. 458 THIRD PART.—BACTERIA OR SCHIZOMYCETES. a. Regard being had solely to the shape of the isolated cells or to their simplest genetic union,— 1. Cocci: isolated cells which are isodiametric or at least very slightly elongated in one direction. ‘These are distinguished when necessary according to their dimensions into mzcrococct, macrococct and monad-forms. 2. Rod-like forms: cells elongated in one direction and cylindrical, rarely fusiform, isolated’ or in a short chain. These again are distinguished into short rods (Bacteria), long rods (Bacili), fusiform rods (Clostridia) and some others. 3. Spiral forms: spirally twisted rods, seme with narrrow corls (Spirillum, Spirochaete), some with distant and very steep coils ( Vibriones). It follows necessarily from what has been already stated that no sharp line of distinction as regards their shape can be drawn between short rods, for instance, and cocci, or between a slightly twisted Vibrio and a Bacillus which departs to a trifling extent only from a mathematically straight line; nor can they at present be always clearly distinguished by their structure. This is especially the case with respect to the rod-like forms, since a rod may be a single cell of the corresponding shape, or a number of cells firmly connected together and closely related to one another genetically. In the latter case while the cell is dividing repeatedly, the partition-wall may be of so delicate a structure that the com- pound body, if not carefully examined, may be taken for a simple homogeneous body. Hence when these organisims are simply spoken of as rods we must under- stand that the writer is alluding to their outward appearance only, unless the structure also is exactly described. To these three kinds must be added a fourth, namely the swollen bladder-like forms. Individuals of this kind are found in company with the other three and are evidently produced from them; they are distinguished by having their cell swollen to several times the size of the other form, with a knobbed and irregular outline. These inflated forms have been observed in artificial cultivations where the nutrient substances are in insufficient quantity or are exhausted; Zopf and Cienkowski found them in Cladothrix and Crenothrix, Buchner and Prazmowski in forms of Bacillus, and Neelsen in Bacterium cyanogenum. ‘They are therefore considered to be diseased states of the other forms, and have been termed by Nageli and Buchner involution-forms. Hansen, on the other hand, has shown that they occur very frequently, indeed almost invariably, with the Bacteria of mother of vinegar; we do not know whether they have not some further meaning in this and perhaps also in most other cases. 4. According to the mode of the connection between the individual cells, each of the above form-groups may be,— 1. free, that is not firmly joined together, though occurring in the society of great numbers of like individuals, 2. in the form of filaments, that is joined together and forming long filiform rows. These filaments are unbranched in most Schizomycetes and then the form is known as Leplothrix or Mycothrix ; they are branched in a few cases only (Cladothrix). In the latter form one extremity of a cell bends outward from the row in which it occurs, and continues its growth and divisions in a divergent direction. The CHAPTER X.—MORPHOLOGY OF THE BACTERIA, 459 terminology adopted in the case of the Scytonemeae is also applied to this form of branching in the Schizomycetes, which has therefore been designated by the really in- correct or at least unnecessary name of false branching (pseudo-ramification). In some of the larger forms of this group, Crenothrix for example, Cladothrix, and species of Beggiatoa, the filaments attach themselves by one extremity to fixed bodies, while the other extremity stretches free into the surrounding fluid; here therefore there is a distinction between base and apex, and this is accompanied by certain corresponding phenomena of growth, such as the direction of the branches and some others. a The formation of filaments occurs in those Schizomycetes in which growth and divisions advance only or chiefly in one, and that the longitudinal direction. If these take place alternately in two or three directions while the genetic connection is maintained, then 3. Groups of cells are produced forming flat surfaces or masses. The dice-shaped pockets of Sarcina ventriculi are the best-known examples of this kind. Figs. 170 f x and 175 a will give an idea of their appearance, 4. The isolated and connected forms of each of the kinds described above may again be united by coherent mucilage into larger gelatinous masses, which are known by the older and more general name of Palmella, or by the more recent term of Zoogloea. ‘These masses form gelatinous layers or pellicles according to the species or culture-form, and cover the surface of the solid or fluid substratum ; or. if suspended in a fluid they form lumpy bodies of very various shapes and are often lobed and branched. The gelatinous cell-membranes in these masses are either fused together into a homogeneous structure, or show a stratification which varies in the different isolated cells or aggregates of cells. In the larger and more firmly united masses the cells, whether isolated or connected together, have not the power of locomotion which many of them, as we have seen, possess in the free state. \ All these varieties of shape and connection are merely growth-forms like those designated Filamentous Fungi, Sprouting Fungi, Compound Fungus-body, &c. (see section I), But the Bacteria were at first distinguished into species and genera according to these forms of growth, and on the too hasty assump- tion that the forms produced from them were always like the parents, and since the year 1872 these distinctions have been precisely defined by Cohn. But it is obvious from what has now been stated that we are dealing in the present case with form-species and form-genera only, using these words in the sense assigned to them on page 120; the names Micrococcus, Bacillus, Spirillum, Spirochaete, Vibrio, Leptothrix, Zoogloea and others, applied above to the Schizomycetes, were in this sense used originally as names of genera and not as designations of forms of growth. The relations of these form-genera to the natural genera, that is to the genera founded on the entire course of development, will be considered presently. : Section CXXX. ‘The forms comprised under the name of Bacteria or Schizo- mycetes may be distributed, in accordance with the course of their development. and with the facts as at present known to us, into two groups, and such is to some extent the course adopted by Van Tieghem in his new text-book. The first group will contain the species which have their sporeS’ formed endogenously, the Zmdo- 460 THIRD PART.—BACTERIA OR SCHIZOMYCETES. sporous Bacteria; the second those which have no endogenous spore-formation, the Arthrosporous Bacteria. It has yet to be seen whether this distinction will be permanently maintained. It is evident from the gaps in our present knowledge that many forms are met with whose behaviour in this respect has not yet been ascertained. The distinction therefore is not a convenient one for a purely practical classification of the Bacteria. a. ENDOSPOROUS BACTERIA. The forms included under this term are “chiefly known in the growth-form of single rods consisting of one or a few cells, or of rods joined together and forming long filaments; they may also be collected together into larger gelatinous masses or membranes.. In some forms the rods are spirally twisted, and these I name here Spirillum of Van Tieghem, Others do not show these curvatures, but are either straight or very slightly bent; all these I include under the term Bacillus and place under that genus all the endosporous forms which have been hitherto known either as Bacillus or as Clostridium, Bacteridium, Vibrio, or by some other name. All non-endosporous forms bearing these names on account of their growth- form are of course excluded from the group. The Bacteria in question are distinguished by the peculiar mode of spore- formation. At the commencement of the process the protoplasm of each cell which has hitherto been homogeneous becomes somewhat darker and in some cases visibly granular, and in the forms enumerated on page 455, which however are the smaller number, it gives the amyloid reaction. Then a darker and comparatively very small body makes its appearance in the interior of each cell and soon increases rapidly in volume, acquiring a distinct outline some time before it reaches its ultimate size and becoming strongly refringent. It has now the aspect of a glistening bluish sharply defined dark granule, and continues to grow till it has reached its definite size and shape, which it does in the space of a few hours. As it enlarges,.the surrounding protoplasm or the amyloid substance disappears, and the body when fully developed is surrounded only by a pellucid substance inside the very delicate membrane of the mother-cell; this body may be termed a spore or resting’ spore. In the great majority of observed cases one spore only is formed each time in a cell. The supposed exceptional case’ of two spores being formed in a single cell is rare, and is moreover said to occur in forms which as a rule produce only one spore ; it is possible that the partition-wall between two sporogenous cells may have been overlooked. The sporogenous cell is according to the species either not different from the vegetating cells of the same species or form, or is distinguished by being somewhat thicker and of a different shape; the change of shape is often caused by the appearance of a fusiform or club-shaped enlargement at one extremity, in which the spore is formed. In this case the mature spore is usually much shorter than the mother-cell, and is seen as a glistening body in the enlarged portion of the parent-cell; the apparently empty part of the cell, and in some cases also sterile ? Prazmowski, as cited on page 455.—E. Kern, Ueber ein hep &e. (Bot. Ztg. 1882,. p- 264, and Bull, Soc. Hist. Nat. Moscou, 1882), CHAP, X.—MORPHOLOGY OF THE BACTERIA,—ENDOSPOROUS BACTERIA. 461 cylindrical sister-cells, is attached to the spore as a longer or shorter appendage. Such structures with one swollen sporiferous extremity are. the ‘capitate Bacteria’ of older writers. In other species there is less difference in size between the spore and the mother-cell, though the latter is never quite filled by the spore. In Spirillum amyliferum and Bacillus (Clostridium) butyricus, which show the granulose- reaction before the formation of the spore, the spot where the comparatively small spore begins and completes its formation is, according to Van Tieghem, a terminal portion of the mother-cell in which there is no granulose. The motile forms may continue their movement during the development of the spore; they become stationary as the spore matures, and finally in all cases the membrane of the mother-cell dissolves sooner or later and the Spore, is set at liberty. : . In most of the species which have béin examined the formation of spores coincides with the moment when the substratum has expended its nutrient material or from other causes, such as an accumulation of products of fermentation, has become unfitted to support the vegetation of the species. At the same time the phenomenon does not always depend on the quality of the substratum. Prazmowski has shown that Bacillus butyricus may be in active process of vegetative multiplication while some of its cells are forming and maturing their spores. The formation of spores when once begun extends usually to the greater number of the isolated cells and aggregates of cells in a pure culture; but a certain number of the cells remain sterile, and no definite rule determining their distribution has yet been discovered. The parts which remain sterile are seen to break up and disappear if fresh nutriment is not supplied in time; if it is supplied they may continue to vegetate. Plants grown in quantity in a pure medium and left to themselves often produce enormous masses of ripe spores. The ripe spore varies from round to elongate-ellipsoidal or cylindrical according to the species. It has the appearance, as has been already said, of a highly refringent usually colourless body (reddish in Bacillus erythrosporus, Cohn) with a dark and sharply defined outline; in some cases it looks like an oil-drop, but reagents show that the resemblance to the latter is only superficial. It consists of a highly refriffgent mass of protoplasm, which with our present means of investigation is perfectly homogeneous. This protoplasmic body, as is shown in germination, is closely surrounded by a thin but firm and often apparently brittle membrane; outside the cell-wall may often be seen a pale slightly refringent envelope with lightly marked contour and of apparently gelatinous consistence, the material com- position of which cannot be exactly ascertained, but which forms a delicate covering to the spore, and sometimes also appears to be prolonged at each extremity of the spore into a small tail-like appendage. Pasteur’ was the first who described these appearances but he did not distinctly recognise their significance. The bodies in question are proved by their germination to be spores. They are in a condition to germinate, as soon as they have reached the development described above at the expense of the mother-cell; and they retain the power of 1 Btudes sur la maladie des vers & soie, I, 228. 462 THIRD PART.—BACTERIA OR SCHIZOMYCETES., germination for a considerable time, showing a remarkable degree of resistance to the effects of desiccation, extreme temperatures and the like (see section CXXXIV). Germination commences as soon as the spore is subjected to the conditions required for the nutrition and vegetation of the species, that is, as soon as it is placed in a suitable nutrient solution at a proper temperature. It is completed in-a few hours when the conditions are favourable, and consists chiefly in the development of the spore into a cell which assumes all the characters of the parent-cell as regards conformation and vegetation. The spore at first enlarges in size, loses its high refringent power and becomes pale and turbid, like a bacterium-cell when in an active state of vegetation; it then elongates and assumes the shape characteristic of the species and at once begins to divide like the vegetative cell, and locomotion may commence at the same time. When the elongation has reached a certain small amount, which. is moreover different in different individuals, a membrane dividing usually into two regular valves of equal size is seen in most cases to séparate gradually from the growing cell, being evidently raised off from it by the hyaline gelatinous outer layer of the membrane of the growing cell. The valves are usually thin and pale-coloured; but in Bacillus subtilis they have nearly the same amount of refringent power as the ripe spore, so that it is probable that the latter owes its characteristic appearance to the membrane which is thrown off in germination. The pieces of the detached membrane gradually disappear in the surrounding fluid. In spores which have elongated in the direction of the longitudinal axis of the mother- cell the membrane splits in the same or in the transverse direction. The direction varies with the species; the membrane for example of Bacillus butyricus according to Prazmowski, and of other species, parts longitudinally, that of Bacillus subtilis transversely, The membrane is not thrown off in the above manner in all cases in germi- nation, but is sometimes seen to swell up and finally disappear. I observed this repeatedly in Bacillus Megaterium and Buchner’ saw it in the Bacillus of anthrax. The direction of growth in length of the vegetative cell first developed from the spore in relation to the longitudinal axis of the spore or its mother-cell is the same in all observed cases as that of the spore, whether the spore-membrane bursts longitudinally or transversely, or swells up and disappears. This is tHe case also with Bacillus subtilis, as will be described hereafter at greater length, where according to Brefeld and Prazmowski the first cell usually issues transversely at right angles to the longitudinal axis of the spore from the spore-membrane which has burst om one side. er The above is the course of development observed especially by Brefeld, Van Tieghem? and Prazmowski in many of the species which contain no chlorophyll. It occurs. also in Van Tieghem’s species containing chlorophyll which have been mentioned above. In these the chlorophyll disappears during the formation of the spores and reappears in germination. Whether the bacterium of blue milk is one of this kind is still uncertain after Neelsen’s account* of it and réquires further investigation. * Nageli, p. 272. * See Van Tieghem in Bull. Soc. Bot. 26 (1879), p. 141. ® Cohn’s Beitr. IIT, Hit a * ‘ CHAP. X.—MORPHOLOGY OF THE BACTERIA.—-ENDOSPOROUS BACTERIA, 463 All the above phenomena are in themselves sufficiently simple, and. their course is essentially the same in all the species; but it is nevertheless desirable that we should study a few examples more closely, and see in what light the parts in question present themselves and the form which the specific differences assume. Our first example shall be the large species long known in our laboratories by the name of Bacillus Megaterium. This exceedingly instructive form (see Fig. 194) was first observed in boiled cabbage-leaves used for the cultivation of Myxomycetes and species of moulds, and was afterwards studied in pure cultures in water or gelatine mixed with 7-10 per cent. of grape sugar and a small quantity of meat-extract and also in a pure 2-3 per cent. solution of meat-extract. The gelatine is liquefied by the Bacillus. Most of the cultures to be és a’ described below were carried out in the eS summer-temperature of an ordinary room, & that is, not much above or below 20° C. This species forms small rods 2-5 p» in thickness and cylindrical in. shape with the ends rounded off. The rods, which do best when obtained from spores, grow rapidly in a fresh nutrient solution where they have no competitors to disturb them, and become usually 4-6 times longer than they are broad; then.they separate by trans- ~ Fic. 194. Bacillus Megaterium. a outline of a motile “a . . chain of rods in active vegetation. 4 a pair of motile rods in verse division into two halves or into two active vegetation. # a quadricellular rod in the state of 4 . . after treatment with alcoholic solution of iodine. c a five- unequal parts, which again grow to rods Of celled rod in the first preparation for forming spores. d@—/ - ° . . successive stages of a pair of rods while forming spores, @ the size above mentioned (Fig. 194 @, 5). about two o'clock in the afternoon, ¢ about one hour later, °! Jan hour later thane. The spores in formation in fare ripe A single rod floating in the solution usually ‘towards evening; no others were formed, the one which e . apparently began to be formed in the third cell from the top appears in these circumstances even under ind andc has disappeared; the cells in f which did not con. » ‘ “fs tain spores perished by about nine o FIG. 196, Crenothrix Kiihniana. a—ecocci or spores, ¢—e cocci dividing. / cocci collected into a group and connected together by a gelatinous substance (‘zoo- gloea’),the contour dark. # agroup of cocci developing into filaments. 7—+ filaments of various forms and stoutness attached below to a substratum ; #z—r show the for+ mation of the common sheath round the single members ; g and # separating above into members; ~ with the upper members becoming successively broader and com- paratively shorter, the uppermost mem ving sep d by longitudinal divisions into round spores (‘cacci’), which have escaped at the upper’ end from the sheath, g£ cocci-zoogloeae. After Zopf. g natural size, the rest magn. 600 times. which has already been described. iron as is found in ‘the jelly of the zoogloea-forms. The single rod-like cells within their sheaths pass by repeated transverse bi- partitions into the form of nearly isodiametric mem- bers, which then round themselves off. The mem- bers in the thicker filaments often assume a flat disk-like ‘shape, and then divide into 2-4 small cells by walls parallel to the longitudinal axis of the filament. Both these cells and the rounded members of the slenderer filaments ultimately escape in the form of cocci from the sheath, being set free partly by the swelling of the sheath along its whole length, partly by its rupture at the apex (r). In the latter case some of the cocci slip of themselves out of the opening in the sheath, while others are passively thrust out of it by the growth in length of the other parts which remain in the sheath. The cocci may, though they rarely do, become motile, and pass again out of this state into the resting zo0o- gloea-form; they also de- velope once more into rods and filaments in the manner In addition to these forms curved spirilla-like forms are also found, which may also break up into pieces, but without passing, as far as has been at present observed, into the motile state. CH. X.—MORPHOLOGY OF THE BACTERIA.—ARTHROSPOROUS BACTERIA. 471 Beggiatoa alba (Figs. 197,198) forms filaments which in an intact state are attached in an erett position to fixed objects in dirty water, in water discharged from factories, andin hotsulphursprings. The filaments vary in thickness from r to more than 5 », and consist of a single row of cells, the protoplasm of which con- tains granules of sulphur in quantities differing in each cell (see page 455) 3 when the sulphur is very abundant it may be diffi- cult to perceive the boun- daries between the cells. The filaments have no separate common sheath and readily divide trans- versely into pieces. Their cells pass successively from the lengthened rod- form into the isodiametric form, and these in the case of the thicker fila- mentsinto flat discs which finally divide by longitu- dinal walls into four quad- rants (Fig. 127, 6-8). The disc-like cells as well as the isodiametric members of the slender filaments separate after a time from one another (Fig. 197, 9) and round themselves off, and then become active swarm- cells (Fig. 197, 10); at length they come to rest and attach themselves to fixed objects. They mul- tiply abundantly by bi- partition and form irregu- ks ae ae : o§ ee ee Saas SDS petals rao SbeeclnesD a aol & sé SSS: x ie MiAIRe GalelelélslesiolGlels a wa (3) io! eke oath The. ecesolle >) i ala aR Oo BE EPP am LE apg FFE eGo CRB, BU® CER proike Se & rs 6 FIG. 197. Beggiatoa alba. 1 group of attached filaments. 2—5 portions of filaments of different stoutness, 5 in the act of breaking up into fragments. The small dark circles in the interior are granules of sulphur; in the parts of the filaments where the granules are abundant the transverse seg ion is indistinct, in others it is more clearly seen. 6—8 fragments rich in sulphur showing the transverse septation clearly after treatment with methyl-violet solution ; in 8 the longitudinal division also is shown in the separate members (formation of cocci or spores). 9 filaments which have broken up into spores. 10 spores in states of movement. The dark circles are in all cases granules of sulphur. After Zopf. I magn. 540, the rest of the figures goo times. larly-shaped zoogloea-heaps. They may also develope into rods and these again into the filaments above described after the rods have in many cases themselves passed through the swarming-state. In this species also spirally twisted filaments are found as well as the straight ones which we have been hitherto considering, 472 THIRD PART,—BACTERIA OR SCHIZOMYCETES. and these break up into fragments containing from two to several coils and exhibiting active movement; they were formerly known by-the name of Ophidomonas, and are said to have a long oscillating cilium at each extremity (Fig. 198 Z). The same states have been observed in Beggiatoa roseo-persicina as in B. alba; the net-like zoogloea-form, once known as Clathrocystis, is a peculiar and remarkable feature in this species. ~ Cladothrix and Leptothrix buccalis of tooth-caries resemble each other in their development. Further details will be found in Zopf’s descriptions. The Fungi of mother of vinegar, Arthrobacterium aceti and A. Pastorianum (Hansen), must also be placed in the arthrosporous group. They are distinguished it is true, as Hansen has observed, by the occur- rence of many large vesicular cells between the small cocci or rod-cells of a chain, and the almost constant appearance of these cells at once suggests that they are connected with some process of spore-formation. But the observations afford no distinct support to this view, and the phe- nomenon must for the present be classed with those of involution which were mentioned on a former page. The Micrococcus also of Pasteur’s fowl-cholera may also be- long to this group’. Section CXXXII. The fore- going review of the Bacteria will supply us with some safe means of determining the question of the FIG. 198. Beggiatoa alba. Curved and spiral forms. 4 group of specific value of observed forms, attached filaments. 2—H portions of spiral filaments: C, 2, #7 in @ question which is at present the the act of dividing into smaller fragments and without movement; with the separate cells distinctly shown. £ swarming fragment subject of much discussion and which (‘Spirillum’) witha cilium at each end. The sulpbur-granules here as in Fig. 197. After Zopl. Magn.'s4o tinies. must not therefore be ignored in this place. There are two views on this subject which appear at least to be diametrically opposed to one another. One of these is, as it seems to me, incorrectly ascribed to Cohn, and maintains that every Bacterium which occurs in the same growth-form and produces the same effects of decomposition, though this latter point does not strictly fall within our limits, represents a species in the sense in which the word * Pasteur in Comptes rendus, 90 (1880), pp. 239, 952, 1030, and g2 (1881), p. 430. CH, X.—-MORPHOLOGY OF THE BACTERIA,—ARTHROSPOROUS BACTERIA. 473 is used in natural history. The fact is that Cohn in his publication of the year 1872, which laid the foundation for the morphological treatment of the group, distinguished a certain number of genera, Micrococcus, Bacterium, Bacillus, Vibrio, Spirillum, &c., by a series of marks, and-especially by the shape of the individual cells and their simplest forms of connection, and gave the name of species to the several forms which recur regularly within each of these genera, and have a characteristic shape, decomposing effect and other qualities. It appears therefore that what Cohn dis- tinguishes is that which we have named above form-genera and form-species. The other view goes so far in the opposite direction as to deny the existence of distinct species of Bacteria, and to regard their forms as modifications of one species, or, as it may be expressed in other terms, it supposes that they are modifications which may be transformed into one another by breeding. Earlier allusions to this view are to be found, but it was distinctly opposed to Cohn’s classification by Lankester? and Lister in 1873”, and Billroth in 1874 included all forms of Schizo- mycetes with which he was acquainted in one collective species Coccobacteria septica. It subsequently received support from the views which Nageli expressed in 1877 in the words, ‘I have in the last ten years examined some thousands of Schizo- mycetes and I could not maintain, except in the case of Sarcina, that there is any necessity for distinguishing them into so many as two specific forms*;’ he adds however, that he ts far from asserting that all the forms do belong to a single species, and that tt would be rash to express a decided opinion in a matter in which morphological observation and physiological examination are both so defective. We gave utter- ance to similar sentiments in 1882*. He accepts in fact the principle which led Cohn to establish his form-genera and form-species and the species which he founded on physiological characters, namely the necessity for a provisional arrangement, whilst expressly declining to say whether the forms as distinguished by him do actually correspond to real natural history species. Nageli’s words quoted above in full contain a pregnant criticism of the whole point in dispute as far as it has at present been explained. Neither side rests on the only sure foundation, an exact observation of the continuity or non-continuity of the development of the supposed forms or species, and this is especially apparent in Billroth’s work. Without this observation the question cannot be decided; it is more necessary in this case because the forms in question are small and very like one another, and are often mixed up together and liable therefore, unless very carefully observed, to be mistaken one for another. Lankester made some approach to an exact observation of continuity in one case only, in which the characteristic tints of his Bacterium rubescens (Beggiatoa roseo-persicina) showed the connection between the forms with more than usual distinctness. We have before us at present some 1 [Professor Ray Lankester in a letter published in Nature, vol. xxxiii. p. 414 (March 4, 1886), pointing out the significance of his observations upon Bacterium rubescens published in 1873 in relation to the pleomorphism of Bacteria and criticising the statement in the text, says, ‘ I cannot think that he [De Bary] gives a correct statement of my relation to the conclusion which he finally adopts. The view which I put forward in 1873 is precisely that which Professor De Bary now espouses.’ For further particulars the reader is referred to Professor Ray Lankester’s letter.] 2 Both in the Q. J. Micr. Sc., new series, XIII. 8 Die niederen Pilze &c., p. 20. * Unters. ii, niedere Pilze, p. 130, 474 THIRD PART.— BACTERIA OR SCHIZOMYCETES., exact investigations into the morphology and life-history of these plants, It results from these investigations that the forms above described as cocci, rods, filaments, are growth-forms, like a tree or shrub, a Filamentous Fungus, Sprouting Fungus or Fungus-body. It has been shown by Cienkowski, Neelsgn, Hansen and Zopf, that there are species which can assume the different growth-forms one after another, sometimes with astonishing rapidity. R. Koch, Brefeld, Prazmowski, and Van Tieghem, have made us acquainted with other species with greater uniformity of growth, and Buchner has shown that external causes give rise to variations in the same growth-form in one or more of these species. These investigations all confirm the view advanced by Cohn, that there are species of Bacteria corresponding to the species of higher organisms, but the distinctions between them are not those of Cohn’s form-species. ‘There are comparatively wnzform species, though they may be capable of some variation, such as Bacillus subtilis, B. Anthracis and B. Megaterium ; on the other hand there are p/eomorphous species, especially among the arthrosporous Bacteria, which may appear first in one and then in other quite different growth- forms. It may be assumed in cases of variation and great differences of form, that external causes operate to determine the form, and that the growth-form may be the result of an adaptation to varying external agencies, as happens in cases like that of Mucor (see page 154), though the operation of these external form-determining causes has not yet been demonstrated in all cases. In connection with this point it may be considered probable, that the vegetative process of the different growth-forms of a species may cause different results of decomposition in the substratum, and that the decomposing effects of the same form may vary with the substratum. It is with due attention to these considerations that the determination of the species of the Bac- teria must now proceed, we may almost say, begin; it is obvious that this must rest essentially on the morphology of the organisms, while at the same time the physiological relationships must not be disregarded in the course of the investigation. Section CXXXIII. As regards the place of the Schizomycetes in the natural system, it is apparent from the foregoing statements that the course of their development does not point to any close affinity with the Fungi. To say that they are offshoots of the Fungi is to ‘contradict all trustworthy observations’? so flatly, that the view need not be seriously discussed in this place. They are termed Fungi only in the sense of their being Thallophytes which contain no chlorophyll, and with reference only to the vegetative process implied by the absence of chlorophyll, while the course of their development and their classification are entirely disregarded. The species of Bacillus and Spirillum therefore which have been mentioned above as containing chlorophyll are at all events no Fungi. The forms included above under the name of Arthrosporous Schizomycetes show an unmistakeably close affinity with the chlorophyllaceous and phycochromaceous Algae, which form the group of Nostocaceae in the wider use of the term as including the Nostocaceae and Chroococcaceae. This has been generally allowed since Cohn drew attention to the point in 1853, and it has been recently and very fully worked out by Zopf. According to our present knowledge the Arthrosporous Bacteria are 1 See Cohn, Beitr. IT, p. 188. CH, X.—MORPHOLOGY OF THE BACTERIA.—-ARTHROSPOROUS BACTERIA. 475 simply Nostocaceae or Schizophyta which contain no chlorophyll; at the same time the position of the entire group in the general system remains still undetermined’. Of the forms which are here termed Endosporous Bacteria it can only be said at present that they come nearest of all known forms to the Arthrosporous Bacteria, and apparently are very nearly allied to them. It may be repeated in this place that the sharp separation between the two groups rests on the knowledge of them which we at present possess, and may disappear with its extension. ‘Till then the separation must be maintained, and it must remain an open question whether the resemdlance between the two groups really implies close affinity, or whether the endosporous forms may not stand in still nearer relationship to other members of the system. If we look around us under the guidance of ascertained facts for such affinities, we are led once more, as Biitschli has also pointed out®, to the Flagellatae. The arthrosporous form such as Beggiatoa, with their generations alternating between a state of rest and one of swarming movement by aid of cilia, show an unmistakeable resemblance to the simpler forms of that varied group. The mode of forming their spores which is characteristic of the Endosporous Bacteria finds its analogue, as far as we can venture to speak in the present state of our knowledge, only in the formation of the spores or cysts, to use the customary phrase, in the simple Flagellatae * known as Spumella vulgaris, Cienk., and Chromulina. In these species the spore is formed, as in the Bacteria in question, inside and from a portion of the protoplasm of a cell, and this mode of formation occurs nowhere else among the lower Thallophytes. We may at least suspect that a homology is indicated by this in itself only analogous phenomenon, but the facts which have been observed lend no support to the assumption. In dealing with this question we must keep well in mind that we are not equally well acquainted with all portions of the range of organisms included under the name Flagellatae, especially as regards the course of development of the species, and that their affinities must be to some extent obscure and uncertain. For this reason we will not add anything further to the remarks which have now been made. But if we assume for a moment a connection between the Bacteria and the Flagellatae, it is evident that as a consequence the following series of forms converge to the Flagellatae: firstly, the series of Bacteria and Nostocaceae;~ secondly, that of the Mycetozoa (see page 445); ¢hirdly, that of the chlorophyllaceous Algae, with which are connected in ascending line the main series of the vegetable kingdom and of the Fungi as one or more lateral branches *, and perhaps also side by side with the chlorophyllaceous Algae some smaller groups which are now placed with the Chytrideae; /ourthly and lastly the Rhizopoda and the Protozoa with the Animal Kingdom which connects with these in an ascending line. On the above assumption the position of the series of Bacteria in the whole system would be the definite one of a group of organisms linking with the Flagellatae as a common point of commencement and departure, and coordinating with the series of the Algae 1 Bot. Ztg. 1881, 1. 2 Biitschli (as cited on page 453), p. 808. 3 Cienkowskiin Schulze’s Archiy f. mikr. Anat. VII, p. 434.—Biitschli, (as cited on page 453), PP. 797, 816, t. 45. * Bot. Ztg. 1881. se 476 | THIRD PART.—BACTERIA OR SCHIZOMYCETES, or Mycetozoa. This would not affect the relations between the Endosporous and Arthrosporous Bacteria, or between the latter and the Nostocaceae; nor can there be a doubt that the Nostocaceae which contain chlorophyll and phycochrome are in any case further removed from the Flagellatae than the allied species of Beggiatoa and other arthrosporous forms, and that they therefore occupy the other extremity of the whole series, which has received the name of Schizophytes and is the more remote from the supposed point of departure. With respect to the coordination of the Endosporous Bacteria and the rest of the Schizophytes, we can only repeat what has been already said, that the final determination of the point must be deferred till we are in possession of more perfect knowledge of single forms. CHAPTER XI.—MODE OF LIFE OF THE BACTERIA. Section CXXXIV. Capacity of germination and power of resistance in the spores. All spores of Bacteria in which the point has been investigated are capable of germination from the moment that they are mature, provided that the con- ditions are favourable. If prevented from germinating they show wonderful power of resisting the external agencies which are usually pernicious or fatal to living organisms, and individual spores show this power in different degrees in different species. These points have not yet been sufficiently investigated in the Arthrosporous Bacteria. Kurth’ found that the spores (‘cocci’) of his Bacterium Zopfii are killed in from 17-26 days, when dried in a moderately high temperature (37° C.) and then kept in an air-dry state at the ordinary summer temperature, while the vegetating rods of the same species died in 7 days when subjected to the same treatment. In a heated fluid their death-point is about 56°C. Similar small powers of resistance to desiccation and high temperatures would probably be found in most of the forms, such as Beggiatoa and Crenothrix, which are adapted to vegetate in water. On the other hand the spores of many endosporous forms are instances of the highest powers of resistance. Those of Bacillus subtilis retain their vitality for years when kept in an air-dry condition, and those of B. Anthracis will remain alive, according to Pasteur *, in absolute alcohol and after being exposed for 21 days to the influence of pure oxygen compressed by a pressure of ten atmospheres. We have no precise observations extending over larger periods of time, but Brefeld found the power of germination unimpaired after the lapse of three years when the spores were kept in an air-dry condition, after the lapse of one year when they had Jain in water ; and from these facts as well as on account of other characteristics to be noticed presently, we may safely assume that their powers of resistance are at least equal to those of the most resistent spores of Fungi (page 344). The. spores of ? Bot. Ztg. 1883, 409. * Charbon et septicémie (Comptes rendus, 85 (1877), p. 99). “ CHAPTER XI.—-MODE OF LIFE OF THE BACTERIA. 477 the Bacillus in question also possess wonderful powers of withstanding extremely high temperatures. Even in a fluid they, are proof against a temperature higher than that of boiling water. Brefeld* found that they all germinated after being boiled for a quarter of an hour in a nutrient solution, the greater part of them after half an hour of the same treatment, a smaller number after the space of one hour, none when the boiling had continued for three hours. When spores were heated in nutrient solutions up to 105° C. they were killed in 15 minutes, up to 107°C. in 10, and up to 110°C. in 5 minutes. Fitz found in 1882 that the spores of his Bacillus butylicus (? B. butyricus of Prazmowski) endured a temperature of 100°C. for a period varying from 3 to 20 minutes, according to the special quality of the spores and the medium employed. Temperatures below 100° C. were sufficient to kill the spores when they were exposed to them for a longer continuance. In solution of glycerine death ensued in 2-6 hours at a temperature of 95° C., in 6-11 hours at 90° C., in 7-11 hours at 80°C.; vitality was not destroyed after exposure for 12 hours to a temperature of 70° C. The power of resistance was less in a solution of grape-sugar; the spores were killed in 6 hours at a temperature of go° C. Buchner? found that some of the spores of the Bacillus of anthrax were killed by being boiled in water for two and three hours, and that after four hours’ time they were all dead. Those of Bacillus Megaterium retain their power of germination after being boiled in water for a few minutes. Of spores of less certain derivation occurring in ordinary waters Pasteur states that they can even withstand a temperature of 130°. ‘These facts, and statements of a similar kind occurring in publications on Bacteria, make it probable that the death-point for the spores of the Endosporous Bacteria is generally very high, though it varies with the nature of the medium. But here as elsewhere results obtained in one case must not be at once assumed to be certainly true in others, since Brefeld in the work from which we have quoted has shown that the spores of a form of Bacillus, not B. subtilis, will not live in boiling water. That the spores of Bacteria are able to bear extremely low temperatures has not been proved by direct experiment, but may be concluded from the behaviour of the vegetating cells which will be considered below. The account given in section XCVI of the external conditions of germin- ation is also generally true of the Bacteria, and to this the reader is referred. The minimum and optimum temperature required for germination especially in the Endosporous Bacteria appear to be usually high, other conditions being equally favourable ; at least most of the experiments show that germination does not take place or is very slow in the temperature of an ordinary room, and becomes active only when the temperature is raised. In the case of Bacillus subtilis the minimum is certainly below the temperature of an ordinary room, for germination proceeds in it, though slowly. According to Prazmowski from 30°-35°C, is near the optimum ; I myself have seen spores some days old germinate in the most vigorous manner in a temperature of 40° C. three hours after they were sown. Bacillus 1 Schimmelpilze, IV. * See Nageli, Unters. ii, niedere Pilze (1882), p. 220. ee 478 THIRD PART.—BACTERIA OR SCHIZOMYCETES, Anthracis will not germinate, as far as is known, in the temperature of a room oscillating about 20°; the minimum ig said to be from 35°37°C., and the optimum can scarcely lie much higher. On the other hand dried spores of Bacillus Megaterium several days old germinated without exception in a summer temperature of 20°-25°C. in 8-10 hours after they were sown. The cardinal point is not yet completely established, but the foregoing data suffice to justify the general statements in the introduction to the chapter, and also to show that specific differences exist in the Bacteria as in other groups, and must be investigated in each case. All spores of Bacteria which have been examined resemble those of the Fungi described in page 351 in requiring for their germination a supply of proper nutrient substances in addition to the water which they absorb; they germinate therefore only in nutrient solutions or on a substratum containing water and a nutrient substance. Observation has shown hitherto that the food required to induce germination is qualitatively the same as that which is necessary for vegetative development; at least germination takes place when this food is present, and we do not yet know whether it can take place under other conditions. Section CXXXV. The general conditions and phenomena of vegetation in Bacteria are, as might be expected, analogous with or like those in other plants, especially the Fungi (see section XCVII). Although comparatively few cases* have been carefully examined to determine the relation of temperature to vegetation in Bacteria, it would seem that the range of temperature is great and the optimum usually high. Brefeld* determined the activity of the vegetative process at different tem- peratures by observing in specimens that were well supplied with nutriment how long a time elapsed before a division took place in a rod. He found that with a parity of conditions a rod formed a division every half-hour when the temperature of the air was 30°C., every three-quarters of an hour at 25°C., every hour and a-half at 18.75° C., and every 4 or 5 hours at 12.5°C., while at a temperature of 6.2°C. the vegetative process was extremely slow. The formation of spores required about 12 hours at a temperature of 30°C., an entire day at 22.5°C., two days at 18.75°C., and several days when the temperature was not above 12.2°C.; below 6°C. no spores were formed. Vegetation continues active, according to Cohn® and Prazmowski, at a temperature of 40°-50°C., and is accompanied with energetic movement of the rods. ‘Bacterium Termo’ grows and vegetates according to Eidam* between the temperatures of 5.5°C. and 40°C.; its optimum is 30°-35°C. Koch* states of the Bacillus of anthrax, that in gelatine cultures its growth and spore-formation are finest and most vigorous at a temperature of 20°-25°C. Between 30°C. and 40° C, its growth and the formation of new spores usually come to an end in 24 hours; up to 25°C. the time required for this increases till it reaches 35-40 hours. Below 25° C. the decrease in the temperature is very marked in the negative sense ; at 23°C. 48-50 hours are required for forming the spores, and at 21°C. 72 hours. At 18°C. the first spores appear after about 5 days, at 16°C. after 7 days, and the 1 Schimmelpilze, p. 46. ? Beitr. z. Biol. II, 271. 5 Cohn’s Beitr. z. Lio!. I, 3, p. 208. * Mittheil. aus d. k. Gesundheitsamte, I, p. 64. ” CHAPTER XI.—MODE OF LIFE OF THE BACTERIA, 479 spore-formation becomes constantly more sparing. Growth and formation of spores cease below a temperature of 15°C. Fitz by comparing the forms in a mixture which had completed its fermentation in the same time at different temperatures found that the optimum of his Bacillus butylicus in solution of glycerine was 40° C., that of another species unnamed and grown by itself 37°-40°C. The maximum in both species was 45°-45.5° C. The upper limit of temperature at which vegetating Bacteria can continue to exist appears to be little higher than that observed in the case of most other plants. Cohn found that it approached near to the maximum of vegetation in Bacillus subtilis, being 50-55°C. Fitz found it in the second of his two species just mentioned at about 56°C. According to Eidam, ‘ Bacterium Termo’ was killed when the liquid in which it was vegetating was heated during 14 hours up to 45°, and during 3 hours to 50°. From Buchner’s experiments mentioned above with the Bacillus of anthrax it appears that the dried rods are killed at the same degree of temperature as the spores. Further details will be found in special works on the Bacteria’. The vegetative. forms of the Bacteria are able to bear the lowest temperatures to which they can well be exposed. Frisch? found putrefactive Bacteria and species of Bacillus, among them B. Anthracis, still retaining the power of develop- ment after being frozen in liquid at a temperature of —111° C, It is in accordance with the analogy of other organisms that the temperatures at which Bacteria vegetate and lose their vitality should vary with the character of the substratum. Niageli says* that by making changes in the nutrient solution the death of the Fission-fungi may be ensured within a certain time at any temperature between 30° and 110°, but he does not distinguish here between germination of spores and vegetative states. The Bacteria differ much from one another in respect of the necessity for a supply of oxygen. At one end of the series the vegetation is promoted in the highest degree, other conditions being the same, by the largest possible supply of atmospheric air containing free oxygen; this is the case with Bacillus subtilis, and Arthrobacterium aceti; at the opposite end, as in B. butyricus, it is promoted by the exclusion of free oxygen. Accordingly Pasteur distinguishes between aerobiotic and anaerobiotic vegetation or forms *. Cases have been observed by Engelmann ° lying between these two extremes, in which a less pressure of oxygen is required than that which is afforded by the com- position of the atmosphere. According to Niageli® the aerobiotic forms will also vegetate when deprived of a supply of free oxygen. As regards the proper nutriment of Bacteria it is to be presumed that those which have the green colour of chlorophyll, if they really contain chlorophyll 1 See also Pfeffer, Physiol. II. ? Sitzgsber. d. Wiener Acad., Mai, 1877. * Die niederen Pilze &c. (1877), p. 30, and see also p. 200. * See also on this point Nencki in Journ. f. pract. Chemie, neue Folge, XIX, XX}; also Genning in the same publication. 5 Bot. Ztg. 1882, 321. ® Die niederen Pilze (1877), p. 28. e 480 THIRD PART,—BACTERIA OR SCHIZOMYCETES. assimilate carbon dioxide; and this is confirmed by Engelmann’s observation ' that Bacterium chlorinum gives off a small quantity of oxygen in the sunlight. Nageli’s researches show that the Bacteria which contain no chlorophyll generally require the same kind of food as the Moulds which have been examined, and that the organic compounds employed as food exhibit the same scale of feeding power in the one case as in the other (see section XCVIII) ; but of inorganic nitrogenous com- pounds nitric acid serves as food for the Bacteria, though in a less degree than ammonia. Bodies which are contained in solution in the substratum but are not nutrient substances may greatly influence the vegetation of the Bacteria. It was observed above (p. 354) that an acid reaction in the nutrient solution is as a rule unfavour- able to the development of the Bacteria. Some species however can put up with this state of things to a certain point if they are by themselves in the solution. But their vegetation may be entirely stopped by it, and so Moulds or sprouting Fungi present with them in the fluid may thrive on the acid and overpower the Bacteria. Other bodies, which are products of the decomposition of the sub- stratum caused by the Bacteria and pass into the solution, may also impede the vege- tation as soon as they acquire a certain degree of concentration in the solution. According to Fitz’s observation in 1882, the vegetation of Bacillus butylicus in glycerine solution under otherwise optimum conditions was stopped by 2.7-3.3 per cent. of ethyl alcohol, by 0.9-1.05 of butyl alcohol and by 0.05-0.1 of butyric acid, &c. It should be observed here that bodies which serve as food, and in the case of the aerobiotic forms the oxygen also, act as stimulants on the Bacteria, awakening or accelerating their powers of movement and determining its direction. Engelmann* has shown that sensitive aerobiotic Bacteria are brought to rest by cutting off the supply of oxygen, and are at once set in motion again by renewing the supply, and the movement is directed towards the source of the oxygen, for example a cell containing chlorophyll which is reached by the sun’s rays. An infinitesimal portion of an oxygen-compound, according to Engelmann’s calculation the trillionth part of a milligram, is sufficient to set very sensitive aerobionts in motion, and they are there- fore the most delicate of reagents for the evolution of oxygen. Such sensitive forms, when the oxygen is supplied to them from one direction only, move as close as possible to the source of the oxygen, such as a cell containing chlorophyll or the edge of the cover-glass when a specimen is grown in drops ofa fluid on a microscopic slide. Other forms under the same conditions only approach within a certain distance of the source of the oxygen, and this distance increases as the oxygen diminishes. From this it is concluded that these forms can do with a pressure of oxygen less than that of the atmo- sphere. Anaerobionts behave in this respect in the reverse way to that of the sensitive aerobionts. The movement of motile forms in fluids is similarly quickened by a supply of proper soluble nutrient material, and it is directed, if the supply comes from one side, towards the diffusion-stream of the nutrient solution which flows into the liquid substratum from the source of the supply. Hence the Bacteria gather in dense swarms round solid bodies containing nutrient substances when placed in the fluid in which they happen to be present *. Bot. Ztg. 1882. 2 Bot. Ztg. 1881, p. 441; 1882, pp. 663, 419. ’ Further details will be found in Pfeffer in Unters, d. Bot. Inst. z. Tiibingen, I, Heft 3. CHAPTER XI,—MODE OF LIFE OF THE BACTERIA. 481 Srction CXXXVI. The Bacteria, apart from the forms which contain chlorophyll and which have not yet been carefully studied, are distinguished according to their actual vegetative adaptation into saprophyles and paraszies, in the sense in which the words were employed in section XCIX. The adaptation of the saprophytic forms presents the same general points of view as that of the saprophytic Fungi. Many Bacteria are, like these Fungi, to some extent organisms which produce oxzdations, combustions of the substratum. The Micrococcus of vinegar or mother of vinegar (Arthrobacterium aceti, Mycoderma aceti) oxidises ethyl alcohol in atmospheric air and converts it into acetic acid; but it may also convert it by combustion into carbonic acid and water’. Bacillus subtilis and as it would appear B. Megaterium also cause similar combustion of organic com= pounds and produce carbonic acid and water. Many others excite characteristic Sermentations, lactic acid fermentation, butyric acid fermentation and the viscous fermentation of sugar, &c., they also act as inciters of pufrefactive processes. For the details of these phenomena, which are the subject of so much discussion at the present day, the reader is referred to the special literature of the Bacteria and of the chemistry of fermentation, to the excellent researches of A. Fitz especially, and those of Nageli and Duclaux, and to Pfeffer’s Physiologie, I, chap. 8. Many Bacteria on the other hand are parasitic in and on living organisms, In the determination and description of their mode of life the same points of view must be taken, and the same divisions and nomenclature applied, as those which were explained at length in connection with parasitic Fungi in speaking of their relations to their host and the effects they produce in it, for the same or quite analogous phenomena occur in both cases. In the succeeding remarks therefore there is a tacit reference throughout to sections CI-CXIII. All parasitic Bacteria live as endophytes in the cavities of the body or in the substance of the tissue of the host. Their structure and growth determine the mode in which they attack the host; they find their way either as spores or in the vegetative form into normal cavities of the body accessible from without or into wounds, and in both places they continue a process of vegetation ; they may also be passively conveyed from wounded surfaces in the bodies of animals into the blood and lymphatic passages, or else they penetrate into the cells and tissue from any surface to which they have been conveyed. The Bacillus of anthrax for instance penetrates into the mucous layer of the intestinal canal?, when it has been carried to it in the animal’s food. The effects of fermentation will have something to do with the perforations thus produced, and the direction of the movement will depend on the co-operation of the chemical and physical qualities of the substratum and possibly of the spontaneous motion of the parasite. All known parasitic Bacteria are simply and for the most part vigorously destruchive in their effect upon their host, if we do not in their case also reckon inflammatory processes (the formation perhaps of tubercles) among phenomena of diseased growth and new formation. Bacteria parasitic on plants have scarcely ever been observed, a fact to which 1 Pasteur in Comptes rend. 54, p. 265, and 55, p. 28.—Niageli, Theorie d. Gahrung, p. IIT. ? See Koch, Mittheil. d. Reichsgesundheitsamts, I, p. 61, [4] : li > 482 THIRD PART.-—BACTERIA OR SCHIZOMYCETES. R. Hartig has already drawn attention. One reason for this may be that the parts of plants have usually an acid reaction. At the same time Wakker? has recently described a disease in the hyacinth known in Holland as the yellow sickness, the characteristic symptom of which is the presence of yellow slimy masses of Bacteria in the vessels. In the resting (autumnal) bulb the masses of Bacteria are confined to the vascular bundles of the bulb-scales; at flowering time they are found also in the leaves, and not in the vessels only but in the parenchyma also, where they fill the intercellular spaces, destroy the cells, and ultimately emerge through the ruptured epidermis and appear on the outside. The case demands a thorough investigation. The Bacteria on the other hand which are parasitic in living animals are, according at least to prevailing views, comparatively. numerous, and the most prominent feature in them is their facultative parasitism. Of this we have instances which have been investigated with some care and may be considered as well established, and it will be well to give here a special account of one of the most important of the number, namely Bacillus Anthracis. The structure and development of this species have been already portrayed in Fig. 195. It attacks the Mammalia, especially rodents and ruminants, with the exception of some species and individuals; mice, guinea-pigs, rabbits, sheep and cattle are unequally liable to be infected by it in the descending order. It will also attack human beings. It is communicated with difficulty to dogs, more readily to cats. Observers are not agreed as to the degree of liability of birds, frogs and fishes to be infected with it, and we cannot further discuss their statements in this place. We know from Rayer, Pollender and Davaine that it causes the disease known as anthrax in the animals first mentioned. My own experiments on which this account: is partly based were chiefly made on guinea-pigs, and on material obtained from them. When the Bacillus has gained admission into the blood of an animal capable of the infection, it grows and multiplies in the rod-form described above to such a degree that the entire mass of the blood is permeated by these organisms. The animal sickens as the Bacillus multiplies and the result is usually fatal. The Bacillus may find its way into the blood directly by intentional introduction of rods or spores or from accidental wounds; a prick of a needle charged with rods or spores, so slight as not to draw blood, is sufficient to give the infection to a sensitive animal. But it may also reach the blood from the intestinal canal, into which it is conveyed in the natural way only, that is through the mouth with the food. Rods introduced in this way have no further effects, if the digestive passages are without a wound; they probably perish in the acid contents of the stomach. But if spores are introduced the animal takes the infection. The spores pass unharmed through the acid stomach and germinate in the alkaline contents of the intestinal canal, and the rods which are the product of germination are found in the mucous membrane of the canal, having forced their way probably through the lymph-follicles and Peyer’s patches, as Koch supposes. From hence the way is open through the capillaries into the blood-- passages. According to Koch’s. investigations the infection comes much more frequently * Bot, Centralblatt, 14, p. 315. CHAPTER XI.—MODE OF LIFE OF THE BACTERIA, 483 from the intestinal canal in cases of anthrax arising from natural causes, that is, not _ artificially produced. But to understand the life-history of the Bacillus and with it the aetiology of the disease, we must first enquire how the spores find their way into the intestinal canal. It cannot be directly from a diseased or lately deceased animal, because the Bacillus forms its spores neither in the living creature nor inside the unopened carcase}, But it is evident from what has been said on page 466, that the Bacillus may not only germinate and vegetate luxuriantly outside the body of the animal, but that the formation of spores takes place there almost exclusively, or at least, as is proved by every culture-experiment, in the greatest abundance, if there is a proper supply of oxygen and a temperature of 20°-25°C. A sufficient further supply of nutrient substances must also be presupposed, and experiment has shown that these are found in abundance in every variety of dead organic bodies, and not only in substances of animal origin, such as the solid and fluid parts of animals themselves that have died of anthrax, or the bloody excreta of those that are ill of the disease, but also in vegetable bodies in which the reactions are not too acid, such as potatos, beetroot or crushed seeds, &c. It is evident from this, that the Bacillus is not only able to live as a saprophyfe, but that it must adopt that mode of life in order to arrive at a section of its existence of the greatest importance morpho- logically and biologically, namely that in which it forms its spores. It appears further that it can and does readily find the necessary conditions for its vegetation as a saprophyte on the surface of a moist pasture-ground, when it has once found its way there, and can maintain itself there from year to year by means of its spores and of the rods which dry up or are frozen in unfavourable vegetative periods; it is not necessary that the place should be visited by animals. We may readily conceive, how graminivorous animals liable to infection may take in the spores of the Bacillus with their food in such places and become infected, for the Bacillus has the capacity of parasitism. In the case of cattle that feed in herds, if one falls sick others quickly take the infection and the disease becomes epidemic, because the number of Bacilli on the ground is increased by the addition of those in the bloody excreta of the sick animals, the pasture being thereby rendered more dangerous for the herds, and because stinging flies and the like may directly inoculate one animal with the Bacilli contained in the blood of another. It is obvious that under these conditions an animal is in greater danger of infection if it has wounded surfaces whether of the skin or of the mucous membrane of the mouth and digestive canal. Our experience with the domestic animals has taught us that anthrax is endemic in certain localities, and breaks out there spontaneously, at first attacking single animals, apparently without direct infection from others but usually starting from the intestine, and afterwards spreading to other individuals. It is not easy to explain why separate districts should thus be the favoured home of anthrax, and why an organism which seems to be so capable of dissemination should not be found everywhere and be everywhere alike capable of producing disease. The reason may be, as Koch supposes, that the dangerous localities are wet and liable to be flooded, and that the Bacillus grows more abundantly on wet ground than on dry, and is also 1 See Koch, Mittheil. d. Reichsgesundheitsamts, I, pp. 60, 147. 1i2 484 THIRD PART.—BACTERIA OR SCHIZOMYCETES, ~ raised above the surface of the soil by the floods and spread over the plants which are subsequently eaten by the cattle. It is at the same time possible that the Bacillus may also be conveyed to the localities by the bodies of animals which have died of anthrax. This would at all events be more likely to happen in a district which has once been much infected with the fever than in any other. Mice are very susceptible to the disease, and the dead bodies of these creatures and of other small rodents would be especially calculated to propagate the infection. But Pasteur’s sensational hypothesis, that the Bacillus is introduced into the soil by the burial of the bodies of infected animals, and that its spores are then conveyed by earth-worms from beneath to the surface, is not necessary for the explanation of the phenomena in these or any other localities; it is moreover open to the objection that the formation of spores never or scarcely ever takes place, as is urged by Koch, in the unopened body of an animal in the temperature of the deeper layers of soils and with the small amount of oxygen in the air which they contain. The Bacillus here described is shown by its life-history to be a strictly facultative parasite, which only reaches the highest stage of its development in the non-parasitic state, and not only can but actually often does go through the entire course of its development in this state during many generations and even many years. It has been shown that it has a virulent effect at least on the animals above mentioned. Whether it can vegetate in other species of animals without doing them harm is not yet ascertained. But its virulent effects on those animals which suffer from its presence may be diminished by certain methods of breeding, and indeed be weakened till they become quite innocuous. Pasteur first discovered through his experiments on fowl-cholera, and Koch? confirmed his results, that this takes place when the Bacillus is grown in a neutralised nutrient solution, such as a meat-broth, with a plentiful supply of oxygen and at a high temperature. The attenuation of the effects may be carried so far that a mouse, the most susceptible animal with which experiments have been made, can suffer inoculation without being made ill; the attenuation is induced rapidly when the temperature is raised to nearly 43°C. and may be completed in 6 days; at a temperature of 42°C. the cultivation may require to be continued during 30 days, and the process is still slower in the temperature of an. ordinary room. The Bacillus vegetates under these conditions and multiplies without alteration of its morphological characters, but z¢ does not produce spores. Cultures kept at a temperature of 42°—43°C. perish in about a month’s time, but fresh cultures can be obtained from them from 1-2 days before that time has expired. The Bacillus may recover its virulent properties after a certain degree of attenuation, if it finds its way into an animal which is susceptible to the infection and kills it. There is a degree of attenuation in which it is innocuous to full-grown guinea-pigs, but not to very young ones; if the latter are inoculated with the attenuated matter, the Bacillus returns to its state of greater virulence. The data before us do not show whether a return to virulence is possible from the highest degree of attenuation, nor have we any distinct experiments to prove whether the attenuated Bacillus developes at all in the animal which is inoculated with it but continues healthy, or in what manner it developes. It has been assumed that it does develope there, but there are no precise facts on. * See his essay, Ueber d. Milzbrandimpfung, Cassel, 1883, p. 17. CHAPTER XI.—MODE OF LIFE OF THE BACTERIA, 485 which to ground the assumption ; but enough is known for the determination of the practical question of protective inoculation by means of the attenuated Bacillus. We cannot however enter further into this point here, but must refer the reader to medical works on the subject. Be this as it may, it is easy to conceive, in the case of a facultative parasite which is able to adapt itself to nutrient solutions of different concentration and qualitative composition at a temperature of 15°—20° C. and to the blood of a mammal at one of 37°-40° C., that changes in the adaptation and food may be followed by changes in the deleterious effects, which may be supposed to be due to the production of some kind of ferment. An analogous though quantitatively different case is that of Sclerotinia Sclerotiorum described on page 380, in which the capacity for a parasitic life depends on the food supplied to the plant in its young state. We may also compare the Mucorini (page 358), which vary their form and the decomposition which they produce with the medium in which they live, and the Bacterium described by Wortmann’, which gives rise to a ferment capable of dissolving starch if it is supplied with nothing but starch-grains for its food, but ceases to produce the ferment if fed with carbohydrates in solution or with ammonium acetate. In the foregoing description it has been tacitly assumed that Bacillus Anthracis is a distinct species, and the present state of our knowledge requires the assumption. The Bacillus of anthrax has a resemblance to other species, and among them to Bacillus subtilis, which is not a facultative parasite or at least may under certain conditions be a harmless parasite ; it varies also in the breadth and length of its cells and in other respects; but it always remains within the limits of the specific characters, the most important of which are given on page 466, and which distinguish it from other species and especially from B. subtilis also described above. Buchner has maintained, in opposition to this view, that the Bacillus of anthrax and the hay-bacillus may be made to pass one into the other by breeding, and that they are therefore only states of one and the same species. He has not supplied us with the strictly morphological proof necessary to establish this opinion, since he has not taken into consideration the behaviour of the spores of his altered forms in germination, at least in his published communications, and yet this is one of the characteristic marks of distinction. He adopted also the macroscopic mode of cultivation, in which it is not possible to ensure an uninterrupted control of the continuity of the development, or of the accidental mingling of different species. His transformation of the virulent Bacillus of anthrax into the supposed innocuous hay-bacillus was effected in cultures at a high temperature and with a more than ordinary supply of oxygen; the temperature was 36°C., the apparatus employed ensured constant shaking in air, and the solution contained 0.5 per cent. of meat-extract. The transformation was not obtained at a temperature of 25°C. and when the apparatus was not kept in motion. It was evidently Pasteur’s inno- cuous state which was produced in this case, but that is by no means Bacillus subtilis. The results of the reverse transformation appear, according to Buchner’s own account, extremely doubtful. Now that the facultative parasitism and the possible change of virulence in Bacillus Anthracis have been demonstrated, and since _ 4 Zeitschrift f. physiol. Chemie, VI, p. 287. . 486 THIRD PART.—BACTERIA OR SCHIZOMYCETES. it has been further established that species can be distinguished in the Bacteria as in other organisms, the whole controversy has lost the importance which it was once supposed to have. In Buchner’s experiments on the change of the hay-bacillus into the Bacillus of anthrax, Bacilli from an infusion of hay were bred with certain precautions in fresh blood. The macroscopic character of the masses of Bacilli was changed, and intermediate forms were obtained between the hay-bacillus and the Bacillus of anthrax, and strange to say 20 reversion was obtained in the intermediate forms when solution of meat-extract or infusion of hay was substituted as the nutrient fluid. Mice and rabbits were inocu- lated with the altered matter, and some of the creatures experimented on sickened and died of anthrax, but much the larger number did not take the infection. Koch will not allow that the observed disease was true anthrax, and maintains that it may have been a disease which is common in mice and cannot always be at once distinguished from anthrax—a disease known as malignant oedema, and produced by a Bacillus morpho- logically very like the Bacillus of anthrax, which must have found its way into the culture with the hay-bacillus. If we allow that the disease in the cases actually ascer- tained was anthrax and disregard Koch’s doubt on the point, the things to be remembered are chiefly these. By far the largest part of the original material used for the experiment may have been ascertained to consist of Bacillus subtilis; but we have no proof that other Bacilli, lost at first in the overwhelming mass of B. subtilis and practically not distinguishable from them, were not contained along with B. subtilis in the hay-infusion. It would indeed be wonderful if one species, B. subtilis, were on all occasions fhe only form obtained without admixture of any others from a material like hay treated according to a definite procedure, especially as the apparently exceptional security of the procedure, the boiling the hay, offers no certain guarantee, because the spores of other Bacteria as well as Bacillus subtilis are capable of withstanding that temperature, Bacillus subtilis then may be present in the hay-infusion in much the larger numbers, and the forms mixed with it may be comparatively few. But we have to ask whether this numerical relation may not be altered or even reversed in other nutrient fluids, for instance in blood, whether single spores of Bacillus Anthracis may not have been pre- sent in the original material and only after change of cultivation have been in a condition to produce a small quantity of infectious material among the individuals of the other species, and thus occasional cases of infection may have occurred among the instances of failure ; to these questions the data before us afford no certain answer. Allusion has been already made to Koch’s views, and we will not draw attention here to other points of difficulty, The reader is referred for further particulars to the original publications, The Bacillus of anthrax has been discussed at some length because it is at present the best-known example of the Bacteria which inhabit the bodies of animals and incite disease in them. Modern pathology resting on older observations and experiments, among which the researches into anthrax itself occupy a prominent position, and supported by Nageli’s theoretical considerations, endeavours to refer all infectious diseases in animals, excepting the few that are caused by Fungi (p. 376) and some that were not formerly supposed to be infectious, to the invasion of Bacteria as their proximate cause. These organisms have been sought for sometimes with great, even with excessive zeal, and some have been found, The parasitic qualities, in virtue of which many of these organisms incite disease, have been sufficiently proved in a number of cases, for example in septicaemia, erysipelas, recurrent fever in warm- blooded animals, Pasteur’s fowl-cholera, the flacherie of the silk-worm, though our botanical knowledge of the plants themselves is still very defective. Some forms are still the subjects of lively discussion on the part of experimental pathologists, Bacteria CHAPTER XI.—MODE OF LIFE OF THE BACTERIA. 487 occurring in a living or dead body are not necessarily the inciters of disease, and the attempt to decide the point experimentally often encounters great difficulties. To expatiate further in the domain of pathology would carry us beyond the limits to which we are confined. But we shall perhaps contribute something of value to the above-mentioned discussion as well as to the determination of the recognised cases if we append a few short general remarks to the foregoing account of anthrax. For further details the reader is referred to medical works and to the compilations of Marpmann and Zopf, which are not however as complete as might be wished. So far as can be judged from the accounts before us, all the Bacteria which are suspected of being or are proved to be parasites with the power of inciting disease, with one exception which will be noticed again below, are capable of vegetating and being bred in dead organic matter ; some form their spores chiefly or exclusively in’ this saprophytic stage of their development. The Bacteria of the latter category are therefore facultative parasites like the Bacillus of anthrax, and the rest perhaps are so too; if not, they are at any rate facultative saprophytes. Hence they can both vegetate, like the Bacillus of anthrax, outside the living animal; the localities must be ascertained in each separate case, and it follows that the danger of infection is different in this case and in that of obligate parasitism. Further it will depend on the species, race and individual among the Bacteria in question in their quality of parasites what hosts they will choose, as is the case with the Bacillus of anthrax; or conversely, some species of animals or some individuals will be more liable to be attacked by a given species of Bacterium, while others will be secure from it. It is at the same time conceivable that this condition may vary in individuals, an individual not before susceptible may for instance become susceptible ; this may be due to external causes whether otherwise injurious or apparently indifferent. We have sufficient proof that such changes do actually occur. As the disposition of the host may vary, so also a change may take place in thé qualities, and specially in the virulence of the parasite, as we see in the case of the attenuated Bacillus of anthrax. This may perhaps be assumed to be the general rulé in the forms which approach near to that species and of which we are here speaking. The change may be in the direction of loss of virulence, or on the contrary of its recovery. It may therefore also happen, that experiments in artificial infection with the same forms of Bacterium may, ceteris paribus, yield different results, some of a positive, others of a negative character. It is possible that the great difficulty or impossibility of obtaining animals that are exactly alike for experiments may at least help to heighten the apparent contradictions. The investigation of the Bacillus of anthrax has further shown that the changes just mentioned may be accomplished in a form which would be considered by a naturalist as distinctly speczfic, and which at the same time maintains its specific characters within the limits of variation to which it is subject. Such changes there- fore afford no ground for doubting the existence of distinct parasitic species. From all other trustworthy sources of knowledge we obtain the same testimony, that real species can and must be distinguished in the Bacteria exactly as in other groups of plants and animals, and that the parasitic forms which incite disease do not differ in this respect from the rest. Niageli’s words’, ‘ if my view is correct, the same species 1 Niedere Pilze (1877), p. 64. 488 THIRD PART.—BACTERIA OR SCHIZOMYCETES. assumes in the course of generations various morphologically and physiologically unlike forms one after another, and these forms, in the course of years and decades of years, may produce souring in milk, butyric acid in sauerkraut, ropiness in wine, putre- faction in albumen and decomposition in urine, may turn articles of food containing starch red, and give rise to diphtheria, to typhus, to recurrent fever, to cholera, to intermittent fever’—these words or the view which they embody would not have been published even in 1877, if their author had studied the forms in question, and especially the parasitic forms, with greater attention. At the present day, when our knowledge of the facts is still more advanced, such a position can no longer be maintained. It is specially in the domain of the parasitic Bacteria that investigation has established more and more distinct species, and shown that every disease incited by a parasite which has been thoroughly examined may be traced to a definite form of Bacterium, of the specific character of which there can be as little doubt as of that of a large Fungus or ofa worm. The assertion that there are distinct species of parasitic Bacteria, and that every special disease caused by Bacteria is the work of a distinct species, is not merely a convenient form of statement, as Nageli thinks, but it is the only one which is in unison with the fac/s as at present known. If a species like the Bacillus of anthrax also vegetates as a saprophyte, it is obvious that it may set up different processes of decomposition in the dead substratum from those which constitute disease in a living body. Further, if diseases supposed to be due to the presence of Bacteria ‘have a limited duration in the history of the human race, change, arise and disappear,’ this is no objection to the observed facts but merely a reason for making special efforts to explain them ; and accepting the fact, equally well observed, that men as well as Bacteria may change some of their qualities in the course of time and yet retain their specific characters unaltered, we may suppose that the attempts at explanation will possibly in course of time be successful. It is uncertain whether there are obligate as well as facultative parasites among the Bacteria, either species that are strictly obligate or some that have also a narrowly limited power of saprophytic vegetation. The forms which may possibly excite diseases that are strictly contagious, smallpox for example, should be tested on this point. Mention must be made in this connection of Spirochaete Ober- meyeri, one of the most characteristic parasites and an undoubted inciter of disease, which appears invariably in the blood of those who are suffering from recurrent fever. It has been successfully transferred from men to apes, but to no other species of mammal on which the experiment has been tried. It has been attempted to cultivate it outside the body of a living animal, but as yet without success '. It is very doubtful whether the minute organism, Nosema Bombycis, Niageli, Panhistophyton, Lebert, which accompanies and according to Pasteur’s experiments causes the destructive disease in the caterpillar of the silkworm known as pébrine or gattine, belongs to this group. It appears in the form of small ellipsoid or somewhat elongated peculiarly refractive bodies resembling Bacteria, which may penetrate through all parts of the caterpillar and butterfly. We learn from Pasteur that it may find its . 1. Heydenreich, Unters. ii. d. Parasiten d. Riickfalltyphus, Berlin, 1877.—Lachmann in Deutschen Arch, f. klin. Medicin, 27+ P p- 2b. CHAPTER XI,—MODE OF LIFE OF THE BACTERIA, 489 way into the membrane of the intestinal canal if supplied to a healthy caterpillar with its food, appearing there first singly and then multiplying rapidly and spreading through other organs. Its development and even its mode of multiplication, which is said to be by bipartition, is not yet clearly ascertained, and we can only affirm with Pasteur that it is a highly dangerous parasite, and expect more distinct conclusions from further investigations’. The above case must not be confounded with the forms of disease included under the name of flacherie. These are due, according to Pasteur?, to the disturbances in the digestive process caused by decomposition or fermentation of the food in the intestinal canal, through the presence of an endosporous rod-shaped Bacterium and a chain-forming Micrococcus, the M. Bombycis of Cohn*. Doubtless this is a case of facultative parasitism, though further investigation is desirable. LITERATURE OF THE BACTERIA. The literature of the Bacteria has increased to an enormous size in the last ten or fifteen years. I have taken some pains to make myself acquainted with it, but I cannot affirm that my efforts have been entirely successful. It is at present quite impossible, ~ especially in the medical part of the subject, for scientific criticism to keep pace with the eager study of the Bacteria, while on the other hand it is not the object of this work to supply a mere index. For these reasons I have avoided first of all touching further on the medical side of the question than was required to complete the account of the morphology and biology of the Bacteria; and in the second place I abstain from attempting a complete enumera- tion of the literature of these organisms. Copious notices of it are to be found in the following works :— A. MAGNIN, Les Bactéries, Paris, 1878. W. Zopf, Die Spaltpilze, 2nd ed., Breslau, 1884, in Schenk’s Encyclopadie. G. MARPMANN, Die Spaltpilze, Halle, 1884. DUCLAUX, Chimie biologique (Vol. IX of the Encyclop. Chim. of Frémy, Paris, 1883). The lists of works in the last three books are far from being complete, but by consulting them and the works which will be cited presently every student will find his way to whatever part of the subject is of immediate interest to him. The reader there- fore is referred to these publications as the most important, and after them to the medical ‘ Journals, Annual Reports and recent Text-books, and finally to Just’s Botanischer Jahresbericht ; and in the subjoined list I confine myself to noticing the chief sources of information, which with my own researches have served as the foundation for the account of the morphology and biology of the Bacteria given in the text. A few works already quoted in the notes to the text and referring to special points are not mentioned again below. 1. General literature of the Bacteria. L. PASTEUR, Examen de la doctrine des gén. spontanées (Ann. Chim. sér. 3, 64, and Ann, d. sc. nat., Zoologie, sér. 4, XVI, extracted in Flora, 1862, p. 355) ;—Id., Etudes sur le vin, Paris, 1866 ;—Id., Maladies des vers & soie, Paris, 1870;—Id., Etudes sur la biére, Paris, 1876. 1 Pasteur, Etudes sur la maladie des vers 4 soie, Paris (1870), I, p. 207. The earlier literature of the subject will be found there. See also Frey u. Lebert in Vierteljahrsschrift naturf. Ges. Ziirich, 1856.—De Quatrefages, Mém. de Acad. des Sciences, XXX, 1860.—Leydig in Du Bois-Reymond’s u. Reichert’s Arch., 1863, p. 186.—Hoffmann, Mycol. Ber. (Bot. Ztg. 1864, p. 30). 2 Etudes sur la maladie des vers & soie. § Beitr. z. Biol. I, 3, p. 165. 490 THIRD PART.—BACTERIA OR SCHIZOMYCETES. Also communications of Pasteur, his pupils and opponents since 1858 in the Comptes rendus of the Paris Academy. Among these the remarkable and finished treatise, Sur la choléra des poules (Cptes. rend. 90 (1880), pp. 239, 952, 1030) should be especially noticed. See also below in the second list. F. COHN, Unters. ii. d, Entwicklungsgesch. d. mikroskop. Algen u. Pilze (Nov. Act. Acad. Leop. 1854, 24, p. 1;—Id., Unters. ii. Bacterien (Beitr. z. Biol. d. Pflanzen, I, Heft 2, p. 127, Heft 3, pp. 141, 208, II, p. 249.)—Koch, Schréter, Eidam, in the same publication, Vols. I, Il, Wernich, Miflet, Mendelsohn, Neelsen, in the same publication, Vol. III). L. CIENKOWSKI, Zur Morphol. d. Bacterien (Mém. Acad. St. Pétersbourg, XXV, No. 2, 1877). E, WARMING, Obs. sur quelques Bactéries qui se rencontrent sur les cétes du Danemark (Videnskab. Meddelelser fra Nat. Forening, Kjobenhavn, 1875-6). R. Kocu, Zur Aetiologie d. Wundinfectionskrankheiten, Leipzig, 1878. C. v. NAGELI, Die niederen Pilze in ihren Beziehungen zu d. Infectionskrankheiten, Miinchen, 1877 ;—Id., Unters. ii. niedere Pilze a.d. pflanzenphysiol. Instit. z. Miinchen, 1882. P. VAN TIEGHEM in Bull. de la Soc. bot. de France, 26 (1879), pp. 37, 144, and 27 (1880), pp. 148, 174;—-Id. in Ann. d. sc. nat. sér. 6, VII (Leuconostoc) ;—Id., Traité de Botanique (1883), p. 1108. E. C. HANSEN, Meddelelser fra Carlsberg Laboratoriet, I, Kopenhagen, 1878-82. BREFELD, Bot. Unters. ii. Schimmelpilze, IV. A. PRAZMOWSKI, Unters. ii. d. Entwicklungsgesch. u. Fermentwirkung einiger Bac- terien-Arten, Leipzig, 1880, and in Bot. Ztg. 1879, p. 409. A. F1Tz, Ueber Spaltpilzgahrungen in Ber. d. Deutschen Chem. Ges. I. Jahrg. 9 (1876), p- 1348.—II. J. 10 (1877), p. 276.—III. J. 11 (1878), p. 42.—IV. Ibid. p. 1890.—V. J. 12 (1879), p. 474.—VI. J. 13 (1880), p. 1309.—VII. J. 15 (1882), p, 867.—VIII. J. 16 (1883), p. 844.—IX. J. 17 (1884), p. 1188. W. ZopF, Unters. ii. Crenothrix polyspora, d. Urheber d. Berliner Wassercalamitat, Berlin, 1879 ;—Id., Zur Morphol. d. Spaltpflanzen, Leipzig, 1882. KURTH, Bacterium Zopfii (Bot. Zeitung, 1883). MITTHEILUNGEN d. kais. Gesundheitsamts, I (1881), II (1884). 2. Anthrax. O. BOLLINGER in Ziemssen’s Handb. d. speciellen Pathologie u. Therapie, III (1874), and Pasteur, Comptes rend. 1877, 84, may be consulted for the earlier literature. PASTEUR, Maladie charbonneuse (Cptes. rend. 84 (1877), p. 900) ;—Id., Charbon et sep- ticémie (Cptes. rend. 85 (1877), p. 99); see also Cptes. rend. 87 (1878), p. 47, and Bull. de l’Acad. de Médecine, 1878, pp. 253, 497, 737 ;-—Id., Chamberland et Roux, Cptes. rend. 92 (1881), pp. 209, 429, 266, &c. R. Kocu, Die Aetiologie d. Milzbrandkrankheit (Cohn’s Beitr. z. Biol. II, 277) ;—Id., Mittheilungen a. d. k. Reichsgesundheitsamt, I. H. BUCHNER in Nageli’s Unters. ii. niedere Pilze, 1882 (see previous list). OEMLER, Experimentelle Beitr. z. Milzbrandfrage (Arch. f. Thierheilkunde, II-VI). ARCHANGELSKI, Beitr. z. Lehre v. Milzbrandcontagium (Centralblatt f. d. medicin. Wissensch. 1883, p. 257). ROLOFF, Ueber Milzbrandimpfung u. Entw. d. Milzbrand-Bacterien (Archiv. f. Thierheil- kunde, IX (1883), p. 459). EXPLANATION OF TERMS. Abjection (Abschleuderung) of spores. Throwing off with force of spores from a sporophore. Abjoint. To joint off or delimit by septa. Abjunction (Abgliederung). Delimitation by septa of portions of a growing hypha as spores. Abscise. To cut off or detach by solu- tion of a zone of connection. Abscision (Abschniirung) of spores. Detachment of spores from a sporo- phore by disappearance through dis- organisation or otherwise of a connecting zone. Accessory gonidia. In Mucorini: goni- dial formations found in some species in addition to the typical ones of the group. Actinomycosis. A disease in animals and man characterised by the development of tumours in the jaw-bone, vertebrae, lymphatic glands and other places within which sulphur-yellow bodies like sand- grains occur, each consisting of an aggre- gate of an organism, Actinomyces, which is supposed to be a Fungus. Acrogenous. (a) Producing at the summit, (6) Produced at the summit. Acrogonidium. Gonidium formed at the summit of a gonidiophore. Acropetal. In the direction of the summit. Comp. basipetal. Acroscopic. Looking towards the summit, i.e. on the side towards the summit. Comp. basiscopic. Acrospore. Spore formed at the summit of a sporophore. Adventitious. Produced out of normal and regular order. Aecidiospore. Spore formed in an ae- cidium. Aecidium. In Uredineae: sporocarp consisting of a cup-shaped envelope (peridium) and a hymenium occupying the bottom of the cup from the basidia of which spores (aecidiospores) are serially and successively abjointed. Aerobiotic. Organisms which require for their vegetation a supply of free oxygen are aeriobiotic. Comp. anaero- biotic. Aethalium. In Myxomycetes: com- pound sporiferous body formed from a large combination of plasmodia. Algal layer. In heteromerous Lichens : green band at the line of junction of the rind and medulla of the thallus in which the cells of the Alga of the Lichen are aggregated. Same as algal zone, goni- dial layer, gonimic layer, stratum gonimon. Algal zone. Same as algal layer. Alveolate. Pitted so as to resemble honey- comb. Amoeboid. Like an amoeba, i.e. a small portion of protoplasm exhibiting creeping movement by putting out and drawing in pseudopodia. Amylogenesis. Formation of starch, Amylum-grain. Starch grain. Analogous. Having the same function. Comp. homologous. Androgynous. Having male and female sexual organs developed on the same branch of the thallus. Comp. diclinous. Androspore. Male spore, i. e. spore which on germination produces a body bearing a male sexual organ. Anaerobiotic. Organisms which can vegetate without a supply of free oxygen are anaerobiotic. Comp. aerobiotic. Angiocarpous. Having a hymenium developed by internal differentiation within the sporophore and from the first covered by a special envelope. Comp. gymnocarpous. Annulus. In Hymenomycetes : portion of ruptured marginal veil or of tissue of the stipe forming a collar orfrill or sheath upon the stipe after the expansion of the pileus. Frequently used to designate the special form distinguished as annulus inferus. Same as ring. 492 Annulus inferus. In Hymenomycetes : collar attached to the stipe below the apex formed by rupture of marginal veil round the margin of the pileus. See annulus. Annulus mobilis. In Hymenomycetes: portion of ruptured marginal veil re- maining as a moveable annular sheath upon the stipe after expansion of the pileus. See annulus. Annulus superus.. In Hymenomycetes : same as armilla. Anther. In Hymenomycetes: old term for eystidium. Antheridium. (a) Male sexual organ. (4) In Hymenomycetes: old term for eystidium. Anthrax. Disease in animals and man excited by Bacillus Anthracis. Aphthae. Same as thrush. Apogamy. Loss of sexual function without suppression of the normal product of the sexual act. Apothecium. Same as discocarp. Appendicula. In Erysipheae: branching hair-like process at the summit of sporo- carp. Archegonium. Female sexual organ with narrow upper portion (neck) pierced by a canal usually enclosing one or more cells (neck-canal-cells) and leading to a basal dilated portion (venter) containing one oosphere (ovum) and a smaller cell ~ at the entrance of the neck-canal (ventral canal-cell). After fertilisation the embryo is developed within the venter. Archicarp. Beginning of a fructification, i.e. cell or group of cells fertilised by a sexual act. Same as ascogonium, carpo- gonium. Areolate. Marked out into small areas or spaces. Armilla. In Hymenomycetes: plaited frill suspended from apex of stipe formed by a layer of tissue separated from the surface of the stipe except at apex, and forming at first a covering membrane of the hymenium, from which it is detached on expansion of the pileus. Same as annulus superus, frill. Arthrosporous. In Schizomycetes: spe- cies which have no endogenous spore- formation are arthrosporous. Asciferous. Bearing asci. Ascocarp. In Ascomycetes: sporocarp producing asci and ascospores ; its three kinds are apothecium or discocarp, peri- thecium or pyrenocarp, and cleistocarp. Ascogenous. Producing asci. Ascogonium. In Ascomycetes: same as archicarp. Ascophore. Sporophore bearing an ascus. See sporophore, EXPLANATION OF TERMS, Ascospore. Spore formed in an ascus. Same as thecaspore. Ascus. In Ascomycetes : large cell, usually the swollen extremity of a hyphal branch, in the ascocarp within which spores (typically 8) are developed. Same as theca. Ascus-apparatus. In Ascomycetes : portion of the sporocarp consisting of ie asci together with the ascogenous cells, Ascus suffultorius. basidium. Autoecious. A parasite which goes through the whole course of its development on a single host of a particular species is autoecious. Same as autoxenous. Comp. metoecious, lipoxenous. Autoxenous. Same as autoecious. Axile. In the axis of any structure. Azygospore. In Mucorini: apogamously formed spore resembling a zygospore. Corda’s term for Basidiogenetic. Produced upon a basi- dium. Basidiophore. Sporophore bearing a basidium. See sporophore. Basidiospore. Spore acrogenously ab- jointed upon a basidium. Basidium. Mother-cell from which spores are acrogenously abjointed. Same as ascus suffultorius, sterigma. Basipetal. In the direction of the base. Comp. acropetal. Basiscopie. Looking towards the base, i.e. on the side towards the base. Comp. acroscopic. Bion. An individual morphologically and physiologically independent. Blastema, Wallroth’s term for the lichen- thallus. Brood-bud. (a) In Lichens: same as soredium. (4) In Archegoniatae : same as bulbil. Brood-cell. Propagative cell, naked or - with a membrane, produced asexually, separating from the parent and capable of developing directly into a new bion. Same as gonidium, conidium. It passes without demarcation into the brood gemma and bulbil. Brood-gemma,. Pluricellular propagative body without differentiation, produced asexually, separating from the parent and capable of developing directly into a new bion. Same as gemma. It passes without demarcation into the brood-cell on the one side, and into the bulbil on the other. Bulbil. (az) In some Fungi doubtfully considered Ascomycetes: small pluri- cellular bodies incapable of germination. (6) In Archegoniatae: deciduous leaf- EXPLANATION OF TERMS. bud capable of developing directly into a new bion. Same as brood-bud. Bulbus. In Hymenomycetes: swollen base of the stipe of the sporophore. Canker. Disease in deciduous-leaved trees caused by Nectria ditissima, Tul., and characterised by malformation of the rind, exhibiting a swollen cushion-like margin and a depressed dead centre. Cap. In Hymenomycetes : same as pileus. Capillitium. Sterile thread-like tubes or fibres, often branched or combined in a net, interpenetrating the mass of spores within a ripe sporogenous body. Capitate. Having the form of a head. Carpogonium. Same as archicarp. Carpophore. Stalk of a sporocarp. Carpospore. Spore formed in a sporocarp. Cellular spore. Same as sporidesm. Cementation (Verklebung) of hyphae. Union of membranes by a narrow slip of cementing substance, so that hyphae are inseparably grown together. Same as concrescence. Cephalodium. Peculiarly shaped bran- ched or convex outgrowth of a lichen- thallus in which algal cells are localised. Chain-gemma. In Mucoreae: gemma having the form of a septate confervoid filament, the segments of which are capable of sprouting. Same as sprout- gemma. Chlamydospore. spore-membrane. Chromidium. Term proposed by Stitzen- berger for an algal cell in a lichen-thallus. See gonidium. Clamp-cell. See clamp-connection. Clamp-connection (Schnallen-verbind- ung). Small semicircular hollow protu- berance attached laterally along its whole . length (or leaving an eye-hole) to the walls of two adjoining cells of a septate hypha and stretching over the septum between them, either communicating with one or both cells of the hypha or completely delimited from both and then forming a clamp-cell (Schnallen-zelle). Spore with a very thick Cleistocarp. Ascocarp in which the asci _ and ascospores are formed inside a com- pletely closed envelope from which the ascospores escape by its final rupture. Coalescence (Verschmelzung) of hy- phae. Complete fusion of the mem- branes of two originally separate hyphae or hyphal branches. Cochleariform. Spoonshaped. Collenchyma. Form of thick-walled parenchyma in which the middle of the lateral walls of the prismatic cells are thin but the angles strongly thickened so as to round off the cavity of the cell. 493 Columella. Sterile axile body within a sporangium. Compound Fungus-body (zusammen- gesetzter Pilzk6rper). Growth-form in which the thallus is constituted by the cohering of the ramifications of separate hyphae. Comp. Filamentous Fungus, Sprouting Fungus. Compound spore. Same as sporidesm. Compound sporophore (Fruchtkérper). Sporophore formed by the cohesion of the ramifications of separate hyphal branches. Comp. simple sporophore. Concatenate. Linked together in a chain, Conceptacle. General expression for a superficial cavity opening outwards within which gonidia are produced. Concrescence. Same as cementation. Conidiophore. Same as gonidiophore. Conidium. Same as brood-cell. Conjugation. Union of two gametes to form a zygote. Conjugation-cell. Same as gamete. Cortex. Same as rind. Cortina. In Hymenomycetes: marginal veil ruptured at its connection with the stipe and hanging from the margin of the pileus as a shreddy membrane. Same as curtain, velum in narrower sense of Persoon. Cross-septation (Querzergliederung). Division of the terminal portion of a hypha or hyphal branch by transverse septa into a number of spore-cells. Crustaceous thallus(thalluscrustaceus). In Lichens: a thallus is crustaceous when it forms a flatcrust on or in thesubstratum, - adhering firmly to this by its whole under surface, so that it cannot be separated without injury. Same as thallus lepodes. Crystalloid. Crystal of proteid. Cup. In Ascomycetes: same as discocarp. Curtain. Same as cortina. Cutis. Same as pellicula. Cyphella. In Lichens: circumscribed pit in the rind on the under surface of the thallus. Cystidium. In Hymenomycetes: large unicellular, often inflated, structure pro- jecting beyond the basidia and para- physes of the hymenium. See anther, antheridium, pollinarium. Dichotomy. Forking in pairs, i.e. cessation of previous increase in length at an apex with continuation equallyin two diverging directions. Comp. monopodium., Diclinous. Having male or female sexual organs developed on different branches of a thallus. Comp. androgynous. Dioecious. Having male andfemale organs on different individuals. Comp. monoe- cious, 494 Discocarp. In Ascomycetes: ascocarp in which the hymenium lies exposed whilst the asci are maturing. Same as apothe- cium, cup. Discus. Hymenium of a discocarp. Same as lamina proligera, lamina sporigera. Dissepiment. Same as trama. Dorsiventral. Horizontally extended so as to have a dorsal and a ventral surface. Ectosporous. Having exogenously formed spores. See exosporous. Comp. endo- sporous. Ejaculation of spores. of spores. Ejection (Ausschleuderung) of spores. Throwing out with force of endogenously formed spores from a sporangium. Same as ejaculation of spores. Elater. In Myxomycetes: a free capillitium thread. Enearpium,. Trattinick’s term for sporo- phore. Endogenous. Produced inside another body. Comp. exogenous. Endogonidium. Gonidium formed within a receptacle (gonidangium). Endophyte. Plant growing inside another plant and parasitic uponit or not parasitic. Comp. epiphyte. Endosporium. Innermost coat of a spore. Comp. exosporium, episporium. Endosporous. Having endogenously formed spores. Comp. exosporous, ectosporous. Entozoic. Living inside an animal. Envelope-apparatus. In Ascomycetes: all the parts of the sporocarp except the ascus-apparatus which consists of asci and the ascogenous cells. Epinasty. That state of a growing dorsi- ventral organ in which the dorsal surface grows more: actively than the ventral surface. Comp. hyponasty. Epiphloeodie. Of Lichens: living upon the surface of the periderm of a plant. Comp. hypophloeodice. Epiphragm. In Nidularieae: delicate membrane closing the cup-like sporo- ‘phore. Epiphyte. Plant growing upon the outside of another plant and either not parasitic upon it or parasitic. Comp. endo- phyte. Epiplasm. Same as glycogen-mass. Episporium. Outer (second) coat of spore. See exosporium. Comp. endosporium. Ergotised. Attacked by ergot. Excipulum. Outer envelope of a disco- carp developed as part of the envelope- apparatus. Exogenous. Produced on the outside of another body. Comp. endogenous, Same as ejection EXPLANATION OF TERMS, Exosporium. (a) Same as episporium. (4) In Peronosporeae: thick coat de- veloped from periplasm around the oo- spore. Exosporous. Having exogenously formed spores. Comp. endosporous. Extracellular. Outside of a cell. intracellular. Extramatrical. Outside of a matrix or nidus. Comp. intramatrical. Comp. Facultative. Occasional, incidental. Comp. obligate. Facultative parasite. An organism which can and normally does go through the whole course of its development as a saprophyte, but which may also go through its development wholly or in part as a parasite. Comp. obligate parasite, facultative saprophyte. Facultative saprophyte. An organism which normally goes through the whole course of its development as a parasite, but which can at certain stages vegetate as asaprophyte. Comp. obligate para- site, facultative parasite. Favus. Disease of the skin caused by Achorion Schénleinii, Remak. Felted tissue. Same as tela contexta. Fertilisation-tube. In Peronosporeae: tube put out by the antheridium which pierces the oogonium and is the channel through which gonoplasm passes from the antheridium to the oosphere. Fibrillose. Having a finely lined appear- ance as if composed of fine fibres. Fibrillose myeelium. Same as fibrous mycelium. Fibrous mycelium. Mycelium in which the hyphae form by their union elongated branching strands (mycelial strands). Same as fibrillose mycelium. Comp. filamentous mycelium, membranous mycelium. Filamentous Fungus (Fadenpilz). Growth-form in which the thallus is con- stituted by a branched hypha alone, i.e. without union with other hyphae. Comp. Compound Fungus-body, Sprouting Fungus.. Filamentous mycelium. Mycelium of free hyphae which are at most loosely interwoven with one another, but without forming bodies of definite shape and out- line. Same as floccose mycelium. Comp. fibrous mycelium, membran- ous mycelium. Filamentous sporophore. Same as sim- ple sporophore. Filamentous thallus (thallus filamen- tosus). Same as fruticose thallus. Flabelliform. Spread out like a fan. Flacherie. Disease of the silkworm due to EXPLANATION OF TERMS. fermentation of food in intestinal canal caused by Micrococcus Bombycis, Cohn. Flagellum. (a) Solitary long swinging process of the protoplasmof a swarmspore. (4) Long whip-like process on the cells of some Schizomycetes. Floccose mycelium. Same asfilamentous mycelium. Foliaceous thallus (thallus foliaceus). In Lichens: a flat, leaf-like, usually lobed and crisped thallus which spreads over the surface of the substratum, but is only attached at one or several scattered points andcan be separated therefore from it without much injury. Same as frondose thallus (thallus frondosus), thallus placodes. Form-genus. A genus constituted by similar form-species. Form-species. Species constituted by a single stage of the life-cycle of a pleo- morphous species and supposed of itself to be the complete representative of a _ species. Formae oxydatae. In Lichens: crusta- ceous forms which have acquired a rust- colour owing to infiltration of a salt of iron. Frill. Same as armilla. Frondose thallus (thallus frondosus). Same as foliaceous thallus. Fructification. Unicellular or pluricellular body developed as a result of the sexual act from an archicarp alone or from adjacent hyphae as well. In the uni- cellular form it is a zygospore or oo- spore; in the pluricellular form a sporo- carp. Fruticose thallus (thallus fruticulosus). In Lichens: a thallus attached by one point only and by a narrow base to the substratum from which it grows upwards as a simple or more usually branched shrub-like body. Same as fila- mentous thallus, thallus thamnodes. Fuliginosus. Sooty. Funiculus. In Nidularieae: cord of hyphae attaching peridiolum to the inner surface of the wall of the peridium. Gamete. Sexual protoplasmic body, naked or invested with a membrane, motile (zoogamete or planogamete) or non- motile, which on conjugation with another gamete of like or unlike outward form gives rise to a body termed zygote. Same as conjugation-cell. Gattine. Same as pébrine. Gelatinous felt (Gallertfilz). gelatinous tissue. Gelatinous tissue (Gallertgewebe). Tis- sue which is slimy owing to the cell membranes being soft and mucila- ginous. Same as gelatinous felt. Same as 495 Gemma. Same as brood-gemma. Germ-cell. First product of commencing germination of a spore. Germ-tube (Keimschlauch). Tubular process put out by a spore in tube-ger- mination at one or more points of its surface which by continued progressive apical growth developes into a hypha forming either a promycelium or a mycelium. Germ-pore. Pit on the surface of a spore- membrane through which a germ-tube makes exit. Gill. Same as lamella. Gleba. Chambered sporogenous tissue within a sporophore. Glycogen-mass. Protoplasm permeated with glycogen, especially in asci. Same as epiplasm. Sometimes shortly termed glycogen. Gonidiallayer. (a) Aggregation of simple gonidiophores to form a _ cushion-like layer or crust. (4) In heteromerous Lichens: same as algal layer. Gonidiophore. Sporophore bearing a gonidium. Same as conidiophove. See sporophore. Gonidium. (a) Same as brood-cell. (4) In Lichens: algal cell of thallus. Same as chromidium. Gonimic layer. Same as algal layer. Gonoplasm. In Peronosporeae: portion of protoplasm of antheridium which passes through the fertilisation-tube and coalesces with the oosphere. Comp. periplasm. Green-rot. Disease in wood characterised by the tissues becoming a verdigris green. Peziza aeruginosa, Pers., is commonly associated with this condition, but its connection with the prominent feature of the disease is still uncertain. Growth-form. A vegetative structure marked by some easily recognised fea- ture of growth characterising individuals: or stages in the life-cycles of types which have no necessary genetic affinity. Thus Sprouting Fungus, Filamentous Fungus, &c. are growth-forms. Gymnocarpous. Having the hymenium exposed when the spores are maturing. Comp. angiocarpous. Gynandrosporous. In Oedogonieae : dioe- cious forms in which the female plant produces androspores are gynandro- sporous. Haustorium. Special branch of a fila- mentous mycelium serving as an organ of attachment and suction. Heliotropism. Phenomena induced in a growing organ by the influence of illumi- nation. 496 Herpes tonsurans. Same as ring-worm, Heteroecious. Same as metoecious. Heteromerous. In Lichens: a thallus with stratified tissue owing to algal cells forming an algal layer and dividing the hyphal tissue into an outer (rind) and an inner (medullary) stratum is termed heteromerous. Comp. homoiomerous, Heterosporous. Having asexually pro- duced spores of more than one kind. Comp. homosporous. Homoiomerous. In Lichens: a thallus with algal cells and hyphae distributed uniformly and in about equal proportion _is termed homoiomerous. Comp. heter- omerous. nf Homologous. Having the same position and development. Homosporous. Having asexually pro- duced spores of only one kind. Same as isosporous. Comp. heterosporous. Hydrotropism. Phenomena induced in a growing organ by the influence of moisture. Hymenial Alga. In Lichens: algal cell in a sporocarp. Same as hymenial gonidium. Hymenial gonidium. Same as hymenial Alga. Hymenial layer. Same as hymenium, Hymenium. Aggregation of spore-mother- cells, with or without sterile cells, in a continuous stratum or layer upon a sporo- phore. Same as sporogenous layer, hymeniallayer. Seealso discus,lamina proligera, lamina sporigera. Hymenophorum. Portion of a sporo- phore which bears a hymenium. Hypha. The element of a thallus in most Fungi; a cylindric thread-like branched body consisting of a membrane enclosing protoplasm, developing by apical growth and usually becoming transversely septate as it developes. Hyponasty. That state of a growing dorsiventral organ in which the ventral surface grows more actively than the dorsal surface. Comp. epinasty. Hypophloeodic. Of Lichens: living in the peridermofaplant. Comp. epiphloeodic. Hypothallus. In crustaceous Lichens: marginal outgrowth of hyphae, often strand-like, from the thallus. Same as protothallus. Hypothecium. Layer of hyphal tissue immediately beneath a hymenium. Same as subhymenial layer. Inception (Anlegung). First beginning. Inner peridium. See peridium inter- num. Intracellular. Inside a cell. Comp. extra- cellular. EXPLANATION OF TERMS, Interweaving (Verflechtung) of hyphae. Union by interwining without firm cohe- sion with one another. Intralamellartissue. In Hymenomycetes: same as trama. Intramatrical. Inside a matrix or nidus. Comp. extramatrical. Involucrum. Persoon’s term for velum. Involution-form. Swollen bladderlike form of Schizomycete, supposed to be a diseased condition of the form with which it is found associated. Involution-period. Same as resting period. Involution-stage. Sameas resting stage. Isogamy. - Conjugation of two gametes of similar form. Comp. oogamy. Isosporous. Same as homosporous. Kernel. In” Pyrenomycetes: old term for the whole of the softer part of the pyrenocarp within the firm outer wall. Also termed nucleus. Lamella. In Hymenomycetes: vertical radial plate on the under surface of the pileus upon which the hymenium is extended. Same as gill. Lamina proligera. Same as discus. Lamina sporigera. Same as discus. Lipoxenous. A parasite that leaves its host and completes its development inde- pendently, and at the expense of reserve of food appropriated from the host is lipoxenous. Comp. metoecious. Lipoxeny. Desertion of a host. Lysigenetic. Formed by disorganisation or dissolving of cells. Macrogonidium. Large gonidium com- pared with others produced by the same species. Same as megalogonidium. Comp. microgonidium. Madura. Disease in man characterised by swelling and degeneration in feet and hands and supposed to be due to Chionyphe Carteri, Berkl., but the causal connection is not definitely made out. Malignant oedema. Disease in animals like anthrax and due to a Bacillus in form resembling Bacillus Anthracis. Marginal veil. In Hymenomycetes: a membrane stretching from the margin of the pileus to the surface of the stipe in the young sporophore and covering over the hymenium. Same as velum partiale. See velum. Medulla. Central tissue within the rind of a Fungus-body. In Lichens: same as stratum medullare. Megalogonidium. Same as macrogo- nidium, EXPLANATION OF TERMS. — Membranous layer. Same as mem- branous mycelium. Membranous mycelium. Mycelium in which the hyphae form by interweaving a membranous layer. Same as mem- branous layer, myceliallayer. Comp. filamentous mycelium, membranous mycelium. Mentagra parasitica. Same as sycosis. Merispore. Segment of a sporidesm. Meristem. Actively dividing cell-tissue. Meristematic. Consisting of meristem. Meristogenetic. Produced bya meristem. Metabolism. The chemical processes inseparably associated with the vital activity of protoplasm. Metoecious. Forms which pass through separate sections of their complete de- velopment upon different hosts are me- toecious. Same as metoxenous, hete- roecious. Comp. autoecious, lipo- xenous. i Metoxenous. Same as metoecious. Microcyst. In Myxomycetes: a resting state of the swarmcells. Microgonidium. Small gonidium com- pared with others produced by the same species. Comp. macrogonidium. Micropylar. Belonging to the micropyle. Microsoma. Small granule embedded in the hyaline plasm of protoplasm and constituting an essential portion of its substance. Monoecious. Having male and female organs on the same individual. Comp. dioecious. Monopodium. An axis of growth which continues to grow at the apex in the direction of previous growth, while lateral structures of like kind are produced beneath it in acropetal succession. Comp. dichotomy, sympodium. Multilocular spore. Same as sporidesm. Muscardine. Disease of the silkworm caused by Botrytis Bassii. Mutualism. Symbiosis in which two organisms living together mutually and permanently help and support one an- other. f Mycelial layer. mycelium. Mycelial strand: See fibrous mycelium. Mycelium, Vegetative portion of thallus of Fungi composed of one or more hyphae. Mycetogenetic. Produced by Fungi. Mycetogenetic metamorphosis. Defor- mation of parts due to Fungi. Mycosis. A disease of animal tissues due to the vegetative activity of species of Eurotium. Myxamoebae. In Mycetozoa: swarm- cells with purely amoeboid creeping motion. [4] Same as membranous 497 Neck.. In Pyrenomycetes: conical or cylindrical prolonged apex of pyrenocarp through which runs the canal leading to the ostiole. Same as tubulus. N ucleus. See kernel. Obligate. Necessary, essential. Comp. facultative. Obligate parasite. An organism to which a parasitic life is indispensable for the attainment ofits full development. Comp. facultative saprophyte, facultative parasite. Ontogeny. Development of an individual. Oogamy. Conjugation of two gametes of dissimilar form. Comp. isogamy. Oogonium. Female sexual organ usually a more or less spherical sac, without the differentiation into neck and venter of archegonium, and containing one or more oospheres (ova). The oospore does not divide to form a proembryo within the cavity of the oogonium on the parent plant. Oosphere (egg, ovum). Naked nucleated spherical or ovoid mass of protoplasm which, after its nucleus has coalesced with the sperm nucleus, developes the oospore. Oospore. Immediate product of fertilisa- tion in oosphere. Ostiole (ostiolum). In Pyrenomycetes: aperture in pyrenocarp through which discharge of spores takes place. Same as pore. Outer peridium. See peridium exter- num. Ovule. In Phanerogams: macrosporan- gium. Panicle. Twice or more branched struc- ture in which the base of each branching is elongated. Paniculate. Having the form of a panicle. Parapbyses-envelope, In Uredineae: same as peridium. Paraphysis. Sterile capilliform hyphal branch accompanying spore-mother- cellsina hymenium. Applied by Phoebus especially to a Gystidium. Parasite. Organism living on or in and at the expense of another living organism (host). Comp. saprophyte. Parthenogenesis. Form of apogamy in which the oosphere (ovum) itself de- velopes into the normal product of fertilisation without a preceding sexual act. Pathogenous. Producing disease. Pébrine. Disease of the _ silkworm caused by Nosema Bombycis, Nag., a bacterioid organism, Same as gat- tine. kK k \ 498 Pellicula. Theseparablerind-layers of some compound sporophores. Same as cutis. Penicellate. Having the form of a pencil of hairs. Periderm. The cork-cambium and its products. Peridiolum. In Nidularieae: chamber eof the gleba, forming a nest of spores, free or attached by a funicle within the peridium of the sporophore. Peridium. General term for the outer en- veloping coat of a sporophore upon which the spores develope in a closed cavity. InUredineaeit envelopestheaecidium and is also termed pseudoperidium, para- physes-envelope. In Gastromycetes termed also uterus, and may be differen- tiated into peridium externum (outer peridium), the outermost layer which opens in various ways and separates from the peridium internum (inner peri- dium) a layer directly enclosing the gleba. Peridium externum. See peridium. Peridium internum. See peridium. Periphysis. In Pyrenomycetes: sterile capilliform hyphal branch projecting from the wall of the pyrenocarp where there is no hymenium into its cavity. Periplasm. In Peronosporeae: protoplasm in the oogonium and the antheridium which does not share in the conjugation. Comp. gonoplasm. Perithecium. Same as pyrenocarp. Phototactic. Taking up a definite position with reference to the direction of incident rays of light. Phylogeny. Development of a species or larger group. Pileus. In Hymenomycetes: primarily, the conical or dome-shaped upper portion of the compound sporophore bearing a hymenium on its under side; now ex- tended to all compound sporophores in which the hymenium looks to the ground. Same as cap. Pityriasis versicolor. Disease of the skin caused by Microsporon furfur, Rob. Plasmodium. In Mycetozoa: body of naked plurinucleated protoplasm exhi- biting amoeboid motion. Plasmatoparous. In Peronosporeae : forms are plasmatoparous when in ger- mination the whole protoplasm of a goni- dium issues as a spherical mass which at once becomes invested with a membrane and then puts out a germ tube. Plastid. Small variously shaped portion of protoplasm of a cell differentiated as a centre of chemical activity. Pleomorphism or Pleomorphy. The occurrence of more than one independent form in the life cycle of a species. Pleuroblastic. In Peronosporeae: forms EXPLANATION OF TERMS. producing vesicular lateral outgrowths serving as haustoria are pleuroblastic. hire Composed of two or more cells. Plurisporous. Having two or more spores. Podetium. In Cladonieae: stalk-like or shrubby branched outgrowth of the thallus bearing exposed hymenia. Pollinarium. Same as cystidium. Pore. (a)In Pyrenomycetes: sameas ostiole. (4) In Hymenomycetes: same as tubulus. Primary lamella of spore. Outermost layer of the coats of a spore representing the original delicate wall of the primordial spore. Primordium, structure. Procarp. An archicarp with a special receptive apparatus, the trichogyne. Promycelium. Short and _ short-lived product of tube-germination of a spore which abjoints acrogenously a_ small number of spores (sporidia) unlike the mother-spore and then dies oft. Prosporangium. In Chytridieae: vesi- cular cell the protoplasm of which passes into an outgrowth of itself, the sporan- gium, and becomes divided into swarm- spores. Prothallium. homologue. Protothallus. Same as hypothallus. Pseudoparenchyma. Symphyogenetic cellular tissue. Pseudoperidium. See peridium. Pseudopodium. In Mycetozoa: a pro- trusion of the protoplasm of an amoeboid body which may bedrawn in or into which the whole mass may move. Puffing (stéuben). Sudden discharging of a cloud of spores. Pullulation. Same as sprouting. Pulvinate. Having the form of a cushion. Pyecnidiophore. Compound sporophore bearing pycnidia. Pyecnidium. In Ascomycetes: a variously shaped cavity resembling a pyrenocarp formed on the free surface of a thallus and containing gonidia which are termed pycnogonidia. See receptaculum. Pyenogonidium. Gonidium produced in a pycnidium. Same as pycnospore, stylospore. Pyenospore. Same as pyecnogonidium, Pyrenocarp. Cup-shaped ascocarp with the margin incurved so as to form a narrow-mouthed cavity. Same as peri- thecium. First beginning of any A thalloid oophyte or its Receptacle (receptaculum). Term of varying signification, most usually imply- ing a hollowed-out body containing other bodies. Has the following special appli- EXPLANATION OF TERMS. cations in this book :—(a) Leveillé’s term for sporophore. (4) Same as stroma. (c) In Ascomycetes: stalk of a discocarp. i") In Ascomycetes: same as pyenidium. é) In Phalloideae: inner portion of sporophore supporting the gleba. (/) In Lichens: cup of the thallus containing soredia. Rejuvenescence. Transformation of whole of protoplasm of a previously existing cell into a cell of a different character. Resin-flux (Harzsticke, Harziiberfiille). Disease in conifer characterised by copious flow of resin with ultimate death of the tree, due to attack of Agaricus melleus. Resting period. Period during which a dormant or quiescent state is exhibited. Same as involution-period. Resting-stage. Stage of dormancy or quiescence. Same as involution-stage. Resting state. Quiescent or dormant condition. Rheotropism. Phenomena induced in a growing organ by the influence of a cur- rent of water. Rhizine. Same as rhizoid. Rhizoid. Delicate filiform or hair-like organ of attachment. Same as rhizine. Rhizomorphous. Having delicate branch- ing form like rootlets. Rind. (a) The outer layer or layers of a Fungus-body. Same as cortex. In Lichens: same as stratum corticale. (4) The outer layers of the bark in a tree with secondary thickening and some- times all the tissue outside the active phloem. Ring. Same as annulus. Ringworm. Disease of the skin due to Trichophyton tonsurans, Malmsten. Same as tinea tonsurans, herpes ton- surans. Rudimentary (rudimentir). An organ or member is rudimentary which remains stationary at a stage of development in which it is in every respect immature. Saprophyte. Plant living on dead organic substance. Comp. parasite. Schizogenetic. Formed by separation of tissue elements owing to splitting of the common wall of cells. Sclerosed. Exhibiting sclerosis. Sclerosis. Induration of a tissue or a cell- wall either by thickening of the mem- branes or by their lignification, i.e. for- mation of lignin in them. Sclerotioid. Resembling a sclerotium. Sclerotium. Pluricellular tuber-like reser- voir of reserve material forming on a primary filamentous mycelium from which it becomes detached when its develop- 499 ment is complete, usually remains dormant for a time, and ultimately produces shoots which develope into sporophores at the expense of the reserve material. In Mycetozoa the sclerotium is formed out of a plasmodium and after its period of rest developes a plasmodium again. Secondary mycelium. Rbhizoid attach- ments developed from the base of a sporophore which are somewhat like the normal mycelium of the species. Semen multiplex. Tulasne’s term for sporidesm. Septate spore. Same as sporidesm. Simple sporophore (Fruchthyphe, Fruchtfaden). Sporophore consisting of a single hypha or branch of a hypha Same as filamentous sporophore Comp. compound sporophore. Soredial branch. Branch produced by the development of a soredium into a new thallus while still on the mother-thallus. Soredium. In Lichens: single algal cell or group of algal cells wrapt in hyphal tissue, which, when set free from the thallus, is able at once to grow into a new thallus. Same as brood-bud. Soredium-heap. Same as sorus. Sorus. Heap or aggregation. (a) In Synchitrieae: heap of sporangia devel- . oped from a swarmceell. (4) In Lichens : heap of soredia forming a powdery mass on the surface of thallus. Spermatiophore. Structure bearing a sper- matium. Spermatium. Male non-motile gamete- cell which conjugates with a trichogyne. The male sexual function of all spermatia is not yet demonstrated. Spermatozoid. Male motile gamete. Spermogonium. Receptacle in which spermatia are abjointed. Spora cellulosa. Same as sporidesm. Spora composita. Same as sporidesm. Spora multilocularis. Same as spori- desm. Sporangiolum, In Mucorini: small sporangium produced in some genera in addition to the large sporangium. Sporangiophore. Sporophore bearing a sporangium. See sporophore. Sporangium. Sac producing spores endo- genously. Spore. Single cell which becomes free and is capable of developing directly into a new bion. Spore-group. Same as sporidesm. Spore-plasm. Protoplasm of a sporangium devoted to the formation of spores. Sporidesm. Pluricellular body becoming free like a spore and in which each cell is an independent spore with power of ger- mination. Same as spore group, com- x k2 FOO pound spore, spora composita, septate spore, semen multiplex, multilocular spore (spora multilocularis), cellular spore (spora cellulosa), pluricellular spore. Sporidium. Spore abjointed on a promy- » celium. Sporiferous. Bearing spores. Sporoblast. Kérber’s term foramerispore. Sporocarp (sporocarpium). Pluricellular fructification, i.e. pluricellular body de- veloped as the result of the sexual act from an archicarp alone or from adjacent hyphae as well, unlike the body which produced the archicarp, and essentially _ serving to the formation of spores. See fructification. Sporogenous. Producing spores. Sporogenous layer. Same as hymenium. Sporophore (Fruchttriger). Branch or portion of thallus which bears spores or spore-mother-cells. Same as recepta- culum of Leveillé, encarpium of Trattinick. Its forms are distinguished as gonidiophore, sporangiophore, ba- sidiophore, ascophore, &c. Sporophyte. In Archegoniatae: the seg- ment in the life-cycle which produces spores. Sporula. Old term for what is designated above as spore. Sprout-cell. Cell’produced by sprouting. Sprout-chain. Chain of cells produced by sprouting. Sprout-gemma. as chain-gemma., Sprout-germination (Sprosskeimung). Germination of a spore in which a small process (germ-cell), with a narrow base, protrudes at one or more points on the surface of the spore, then assumes an elongated cylindrical form, and finally is abjointed as a sprout-cell. Comp. tube- germination. Sprouting. Formation of an excrescence with a narrow base, and of the same character as the parent, at one or more points on a cell, which after enlargement is delimited by a transverse wall either before or after reaching its proper size. Same as pullulation. Sprouting-fungus (Sprosspilz). Growth- form in which the thallus consists of a sprouting-cell or chain of sprouts. Comp. In Mucoreae: same Filamentous Fungus, Compound Fungus-body. Sterigma. (a) Same as basidium. (4) Stalk-like branch of a basidium bearing a spore. (c) Cell from which a spermatium is abjointed. Sterile basidium. In Hymenomycetes : body in the hymenium like a basidium but non-sporiferous and possiblya paraphysis. EXPLANATION OF TERMS, Stipe (stipes). General term for the stalk | of a sporophore. Strand. See mycelial strand. Stratum corticale. See rind. Stratum gonimon. Same as algal layer. Stratum medullare. See medulla. Stroma. Compound Fungus-body having the form of a cushion, crust, foliaceous ex- pansion, or erect unbranched or branched shrub-like body. Same as receptaculum., Stylospore. Same as pycnogonidium. Suberification. Same as suberisation. Suberisation. Transformation of a cell- wall into suberin, i.e. conversion into cork. Same as suberification. Subhymenial layer. Same as hypo- thecium, Subulate. Awl-shaped. Suspensor. In Mucorini ; club-shaped or conical portion of hypha adjoining a gamete-cell after its delimitation. Same as zygosporophore. Swarmeell. Motile naked protoplasmic body. Sycosis. Disease of the skin due to the at- tack of Microsporon Audouini, Rob., and Microsporon mentagrophytes, Rob. Same as mentagra parasitica. Symbion. Organism which lives in a state of symbiosis. Symbiosis. Living together of dissimilar organisms. Symphyogenetic. Formed by union of previously separate elements. Sympodial. Ofthenature of a sympodium. Sympodium. Anaxis made up of the bases of a number of successive axes arising as branches in succession one from the other. Comp. monopodium. Tela contexta (Filzgewebe). Weft of distinct hyphae. Same as felted-tissue. Teleutogonidium. Sameas teleutospore. Teleutospore. In Uredineae: spore formed by abjunction on, but not separating from, a sterigma, producing in germination, which takes place after a resting period, a promycelium. Tetraspore. In Rhodophyceae: one of the spores formed by division of a mother cell into four parts. Thallodic. Belonging to the thallus. Thallus. A vegetative body without dif- ferentiation into stem and leaf. In Fungi is the whole body of the plant not serving directly as an organ of reproduction. Thallus lepodes. Same as crustaceous thallus. Thallus placodes. Same as foliaceous thallus. Thallus thamnodes. Same as fruticose thallus. * EXPLANATION OF TERMS. Theca. Same as ascus. Thecaspore. Same as ascospore. Thermotropism. Phenomena induced in a growing organ by the influence of conditions of temperature. Thrush. Disease of the mucous membrane of mouth,throat and oesophagus inchildren characterised by formation of pustules due to Saccharomyces albicans, Reess. Same as aphthae. Tinea tonsurans. Same as ringworm. Torulose. Swollen at intervals. Trama. In Basidiomycetes: middle tissue in the projections or septa of the sporo- phore which bear hymenium. Same as dissepiment, intralamellar tissue. Tremelloid. Resembling Tremella. Trichogyne. Thread-like receptive portion developed as part of an archicarp. Trophoplast. Same as plastid. Trophotropism. Phenomena induced in a growing organ by the influence of the chemical nature of its environment. Tube-germination (Schlauchkeimung). Germination of a spore in which the first product is a germ-tube. Comp. sprout- germination. Tubulus. (a) In Pyrenomycetes: Same as neck. (4) In Hymenomycetes: tube lined with hymenium on the surface of a pileus. Same as pore. Unicellular. Formed of one cell. Uredo. Hymenium producing uredospores only. Termed also uredo-layer. Uredogonidium. Same as uredospore. Uredospore. In Uredineae: spore formed by acrogenous abjunction on a sterigma from which it separates when mature and on germination produces a mycelium bearing uredospores or uredospores and teleutospores. Uterus. In Gastromycetes: same as peri- dium. Veil. Same as velum. Veines aériféres. Same as venae in- ternae. Veines aquiféres. Same as venae ex- ternae. Velum. In Hymenomycetes: special envelope within which the growth of the whole or a portion of the sporophore takes place. Same as veil, involucrum of Persoon. By Persoon applied to what 501 \ is defined above as cortina. See marginal veil, velum universale. Velum partiale. Same as marginal veil. See velum. Velum universale. In Hymenomycetes sac enclosing the whole of a sporophore as it grows and ultimately ruptured at the apex by the unfolding pileus. Same as volva. See velum. Venae externae. In Tuberaceae: white veins seen on section of the sporophore produced by dense tissue containing air ‘and filling the asciferous chambers. Same as veines aériféres. Comp, venae internae. " Venae internae. In Tuberaceae: dark- coloured veins seen on section of the sporophore indicating the walls of as- ciferous chambers, which are composed of tissue containing no air. Same as venae lymphaticae, veines aquiféres. Comp. venae externae. Venae lymphaticae. Same as venae internae. Volva. Same as velum universale. Witches’ broom. Disease on the silver-fir, birch, cherry, and other trees characterised by the development of a tangle of shoots in a tuft and due to the attack of Peri- dermium elatinum or of Exoascus. Woronin’s hypha. In Ascomycetes: a coiled hypha found in some forms at the place where the sporocarp subsequently developes and probably homologous with an archicarp. Xyloma. Sclerotioid body of varying shape which does not send out branches developing into sporophores but produces sporogenous structures in its interior. Yeast-fungus. Species of Saccharomyces. Sometimes used as equivalent to the growth form distinguished as Sprouting Fungus, but this misuse leads to con- fusion. Zoogloea. In Schizomycetes: colony imbedded in a gelatinous substance. Zoospore. Motile spore. Zygospore. Immediate product of conju- gation of two similar gametes. Zygosporophore. In Mucorini: same as suspensor, eo eed Ne Pie a) casi atte) « oeveineslemoene INDEX. Names, as ‘ Acrasieae,’ ‘ Abrothallus,’ ‘Achlya Braunii,’ with no further addition, refer to the course of development of the Orders, Genera, &c., as described in the second division of the first part and in the second and third parts; those which are followed by some additional word, as ‘ Achlya apiculata, capacity of germination,’ refer to the remaining sections of the book, An asterisk after the number of a page indicates a Figure. Abjection of spores, 68, 72. Abrothallus, 416. Abscision of spores, 68, 69. Absidia, 147, 150, 152. — capillata, 150. —, discharge of spores, 83. — septata, 150. Acarospora, number of spores, 79. Achlya apiculata, capacity of germination, 343. — Braunii, 142, 144. —, discharge of spores, 82, —, formation of swarm- spores, 143. —, ‘pleomorphism,’ 127. — polyandra, 142, 144. — —, germination, 142*. — prolifera, 144, 145. — —, germ-plant, 141*. — racemosa, 144. — —, fertilisation, 142*. —, simple sporophores, 46. — spinosa, 143. — —, capacity of germina- tion, 343. —, swarm-spores, 107. Achlyogeton, 140. — , discharge of spores, 83. —, swarm-spores, 107. Achorion Schoenlinii, para- sitism, 376. Acolium ocellatum, discharge of spores, 98. Acrasieae (Acrasiea), 421, 441, 443. Acrasis, 442. Acrocordia gemmata, 246. — tersa, 246. Acrogonidia, 249. Acroscyphus, discharge of spores, 96. Acrospores, 129. Acrostalagmus cinnabarinus, abjunction of spores, 71. —, formation of gonidia, 65. —, germination, 111. Acrostalagmus cinnabarinus, mycelial strands, 22. —, structure of spores, 103. Actinomyces Bovis, develop- ment and parasitism, 377. Actinomycosis, 377. Adaptations, different, or metamorphosis, 256, 259. Aecidia, 274. —, abscision of spores, 68. —, formation of spores, 66. —., structure of spores, roo. Aecidiospores, capacity of germination, 343, 344. Aecidium Sedi, 282. Aethalieae (Aethaliei), 431, 434, 439. Aethalium, 429,431,4345439- — septicum, 424, 439, 441. See also Fuligo varians, Affinities of Bacteria, 474. — of Fungi, 337, 340. — of Mycetozoa, 442. Agaricineae (Agaricini), 288, 289, 296, 300, 303, 338. —, clamp-connections, 2, 19. —, mycelial strands, 22. —, structure of compound sporophores, 57. Agaricus, 301. —, abjection of spores, 68, 72. — aeruginosus, mycelial strands, 22, 23. — androsaceus, mycelial strands, 22. — arvalis, sclerotia, 42. — balaninus, 304. — campestris, 291. — —, cellulose, 8 — —, development of sporo- phore, 289*, 291. — —, excretion of calcium, Ir, — —, mycelialstrands,22,23. — —, cementation of hy- phae, 4. — cirrhatus, 297. Agaricus cirrhatus, sclerotia, 32, 39; 42- — cyathiformis, develop- ment of sporophore, 56. — deliciosus, 300. —, development of sporo- phore, 55*. ; _ dryophilus, 297. —-—, development of spo- rophore, 55 *. — —, mycelial strands, 22. — fumosus, 304. — fusipes, 297. — —, sclerotia, 42. —, gelatinous membranes, 9, 10, 13. — grossus, germination of sclerotia, 40, 42. — laccatus, 304. — melleus, 302, 329, 341. —-—, commencement of sporophore, 49. ——, development of the veil, 290*, 291. —_—-—, ” gelatinousmembranes, 9. — —, membranes, 12. — —, mycelial strands, 22, 23, 24%. — —, parasitism, 361, 384. — metatus, cellulose-mem- brane, 8. — —, mycelial strands, 22. —, mycelial strands, 22, 23. — olearius, 301. — platyphyllus, strands, 22, 23. — Pluteus, 304. — praecox, 300. — —, mycelial strands, 22, 31 I, — racemosus, 334. —-—, branching of com- pound sporophore, 51. ——, germination of scle- rotia, 40 — —, sclerotia, 42. mycelial 504 Agaricus Rotula, mycelial strands, 22, 23. —, sclerotia, 32. — stercorarius, germination of sclerotia, 40. —, structure of sporophore, tT eee — tuberregium, sclerotia,42. — tuberosus, 297. -— —, germination of scle- rotia, 40. — —, sclerotia, 32, 42. — variabilis, 333, 334. — velutipes, 297. — viscidus, 304. — volvaceus, sclerotia, 42. — vulgaris, 334. — —, development of sporo- phore, 54. — —, structure of lamellae, 301 *, —-—, structure of sporo- phore, 57. Aglaospora, 243. — profusa, germination, 114. — —, number of spores, 79. —, number of spores, 79. Alcoholic fermentation, 270. Algae, course of develop- ment, 121. — of the Lichen-thallus,397, 398. —of the heteromerous Lichen-thallus, 409. Algal layer of the Lichen- thallus, 404. Algal zone of the Lichen- thallus, 404. Alternaria, 229, 252. —, formation of spores, 67*. —, spores, 68, Alternation of bions,124,125. — of generations, 123, 124. Amanita, 292, 296, 297, 298, 338, 340, —, growth of compound sporophore, 50. —, hyphal weft, 3. — muscaria,292,29 3,298,300. — —, cellulose, 8. —-—, coloration of mem- branes, ro. — —, gelatinous membranes, 9, 13. — phalloides, cellulose mem- brane, 8. —rubescens, development of sporophore, 293*, — vaginata, 295. Amoebae, 443. Amoebidium _parasiticum, 170, Amylobacter 455. Clostridium, INDEX, Amylocarpus, 105. Amylum, 7. — in Bacteria, 455. Anaptychia ciliaris, apothe- cium, 188*, 189*. — -—, chemical properties, 407. — —, spores, 98. —-—, structure of thallus, 404, 406. Ancyclisteae(Ancylistei), 132, 139, 170. Ancyclistes, 139. — Closterii, 139. — —, parasitism, 361, 392. Anixia truncigena, discharge of spores, 97. Annual layers in pilei of Poly- poreae, 57. — in hymenia, 307. Annulus, 290. — inferus, 291. — mobilis, 292. — superus, 295. Antheridial branch, 198, 202, 239. Antheridium, 202, 305. Anthers, 305. Anthina, 29. — flammea, cellulose-mem- brane, 8. — —, mycelium, 29. — pallida, cellulose-mem- brane, 8. — —, mycelium, 29. — purpurea, cellulose-mem- brane, 8. — —, mycelium, 29. Aphanocapsa in Lichen- thallus, 398. Aphanomyces, 143. —, discharge of spores, 83. —, formation ofspores,7 4,75. — scaber, 142. —, Swarm-spores, 108. Aphthae (thrush), 377. Aplanes, 144. — Braunii, 142. —, capacity of germination, 343- Apogamy, 123. Apothecia, 187, 239, 401. Appendages ofspores, 102,&c. Archicarp, archicarpium, 49, 121,198, 199, 201, 238, 239. Arcyria, 431, 434, 436, 440. — anomala, capillitium, spore, 437*. ~ — cinerea, 437, 441. — incarnata, 434, 437. —-—, capillitium, spore, 437". — nutans, 434, 437,441. — punicea, 427, 434,437,441 Arcyria Serpula, capillitium, spore, 437 *. Areolation of spore-mem- brane, 100, Armilla (frill, annulus su- perus), 295, 300. Arnoldia, structure of thallus, 412. — minutula, 413. Arthonia epipasta, 416. —, structure of thallus, 411. — vulgaris, 416. — —, origination of thallus, 399. Arthopyrenia, 416. Arthrobacterium, 454, 468. — aceti, 472, 479, 481. — merismopoedioides, 469. — Pastorianum, 456, 472. — Zopfii, 469. Arthrobotrys, 252. —, formation of spores, 64. —, gonidia, 98. — oligospora, simple sporo- phores, 47*. —, spores, 68. Arthrosterigmata, 240. Artotrogus, 135, 232. —, parasitism, 394. Asci, 45, 60, 76, 191, 192. Ascobolus, 190, 198,199, 206, 232, 235, 239. — furfuraceus, 224. — —, compound phores, 186*, 207 *. — —, conditions of germina- tion, 350, 351. — —, ejection of spores, 85, 937741 — —,structure ofspores, 102. —,conditions of germination, 350. —, development of spores, 78. —, ejection of spores, 85, 86. —, germination, 111. —, immersus, structure of spores, 102. —, number of spores, 79. —; puffing, 90. — pulcherrimus, ejection of spores, 86. — sexdecimsporus, 79. —, structure of spores, 105. Ascochyta, 252. Ascodesmis, 186, 201, 221. Ascogenous cells, 186. Ascogenous hyphae, 186, 209, 214, Ascogonium, 198, 213. Ascomycetes, 120, 185, 285. — as Lichen-fungi, 396. —, capacity of germination, 348. —, compound spores, 98. sporo- Ascomycetes, course of de- velopment, 223. —, development of sporo- phore, 197. —, doubtful species, 132, 263. —, envelope - apparatus of sporocarp, 186. —., functionless organs, 256. —, germination, 115. —, hairs, 59. —, impertectly known spe- cies, 238. —, inception of sporophore, 49. —,lipoxeny (desertion of host), 388. —, structure of sporophore in endophytic, 57. Ascomycetous series, 120. Ascophora elegans, resist- ance of spores, 347. Ascospores, 60, 129, 232. —, capacity of germination, 343- —, development, 76. Ascotricha, 211. Ascus, 60. — suffultorius, 61. Ascus-apparatus, 186. Aseroe, 312, 325. — rubra, compound sporo- phores, 326*. Aserophallus, 312, 325, 326*. Aspergillus, 252, 256. — albus, conditions of vege- tation, 353. —, capacity of germination, 348. — clavatus, 253. —-—, conditions of vege- tation, 353. —— —, mycelial membranes, 2i. — flavescens, parasitism, 370. — flavus, 256. ——-, capacity of germina- tion, 344, 348. — —, parasitism, 369. — fumigatus, capacity of germination, 344. — —, conditions of germi- nation, 349. — —, parasitism, 359, 370. — glaucus, parasitism, 397. — niger, 206, 257. — —, conditions of vegeta- tion, 353. ——, effect on the sub- stratum, 358. — —, mycelial membranes, 21. — —, parasitism, 370. — —, secretion of ferment, 355+. INDEX, Aspergillus ochraceus, con- ditions of vegetation, 353. —, parasitism, 360, — purpureus, 206. —, sclerotioid perithecia, 42. —, simple sporophores, 46. Assimilation of carbon diox- ide by Bacteria, 479. Athelia, 22. Atichia, 416. Atractium, 252. Auricularia, 338. — Auricula Judae, 306. — —, basidia, 305 *. — —,formation of spores,62*. — mesenterica, structure of sporophore, 58. — sambucina, 306. Autoecious, 387. Autoecism, 387. Autoxenous, 387. Azygites, 150. Azygospores, 150, 159. Bacidia, 223. Bacillus, 454,458,460,468,473- — Anthracis, 466 *, 476,477, 478, 482, 486. — butylicus, 477, 480. — butyricus, 455, 461, 462, 479- — erythrosporus, 461. — Megaterium, 463*. — subtilis, 457, 462, 466*, 467, 476, 477, 479, 486. — virens, 455- Bacteria, 454. —, aerobiotic, 479. —, affinities, 474. —, anaerobiotic, 479. —, arthrosporous, 460, 468. —, assimilation of carbon dioxide, 479. —, capacity of germination, 476. —., cell-forms, 458. —, course of development, 459. —,endosporous, 459,460,475. —, formation of spores, 460, —, mode of life, 476. —, parasitic, 481, 487. —, resistance of spores, 476. —, saprophytic, 481, 487. Bacteridium, 460. Bacteriopurpurin, 455. Bacterium, 454, 458, 468, 469, 473- — butyricum, 477. — chlorinum, 455. — cyanogenum, 458. — merismopoedioides, 469. — Pastorianum, 456, — Termo, 478, 5°5 . Bacterium viride, 455. — Zopfii, 469, 476. Bactrospora, number of spores, 79. Baeomyces, 200, — roseus, 222. Balsamia, 195. Basidia, 45, 61, 286, 302, 305. —, definitive, 306. —, primary (initial), 306. —, secondary, 306. —, sterile, 302. Basidiomycetes, 120,132,286. —, angiocarpous, 338. —, clamp-connections, 2, 19. —, course of development and relationships, 328. —, formation of spores, 61, 63, 67, 68. —, germ-pores, 100. — gymnocarpous, 289. Basidiospores, 339, 340. —, capacity of germination, 343. Basidium, 60, 61, 306. Battarea, 311. —, capillitium, 8. — Steveni, 317. ——, fibres of capillitium, 317*. —, thickenings brane, 8. Beer-yeast, 267. Beggiatoa, 455, 459,469,475. — alba, 471*, 472*. — roseo-persicina, 455, 472, 473+ Bion, 123. Blastema, 401. Blastenia, 223. — ferruginea, 223. Boletus, 288. —, assumption of a_ blue colour in the air, 15. —, coloration of membranes, Io. — edulis, 301. — elegans, 297. —, gelatinous membranes, 9, 10. — luteus, 297. Botryosporium, formation of spores, 63. —, thallus, 1. Botrytis, 252. — Bassii, 252. of mem- ——, capacity of germina- tion, 344. — —, formation of spores, 65, 65*. — —, parasitism, 362. — cinerea, 224, 238, 252, 254. — —, cell-nucleus, 6, va 506 Botrytis cinerea, conditions of germination, 349. — —, development from a sclerotium, 38, 41. — —, gonidiophores, 48. — —, membrane, 12. — —, organs of attachment, 21. ——~, resistance of spores, 347+ ——, simple sporophores, 48. — —, thallus, 1. — erythropus, development from sclerotia, 41. Bovista, 11, 309, 310, 315. —, formation of spores, 64. — plumbea, capillitium, 12, 314%, 315. Brachycladium, 252. Branching in Bacteria, 458. — of the thallus, 1. Bristles on compound sporo- phores, 59. Brood-buds, 124, 401, 415. Brood-cells, 124, 129, 154. — of Lichens, 417. Bryopogon divergens, in- crustations, 408. — jubatus, 246. — —, colouring matter, 408. —, distribution of Algae in the thallus, 404. —ochroleucus, _incrusta- tions, 408. —sarmentosus, _incrusta- tions, 408. —, soredia, 415. —, structure of thallus, 404, 406. Bulbils, 124, 263. Bulbus, 292. Bulgaria, ejection of spores, 89. —, gelatinous membranes, 9, 13. — inquinans, spores, 91. — —, germination, 115. — sarcoides, 242. — —, ejection of spores, 86. Bursulla crystallina, 446. Byssaceae (Byssacei), 402. Byssocaulon niveum, struc- ture of thallus, 411. Byssus, 29. ejection of Caeoma, 282. — Euonymi, 282. — Mercurialis, 282. — pinitorquum, structure of spores, 100. Calathiscus, 312. Calcareae (Calcariei), 424, 430, 435,436, 441,448,451. INDEX. Calcium carbonate in Myce- tozoa, 435, 436. — — -vesicles, 430. — oxalate, 11*, 408. Callopisma, 223. Calocera, 288, 305. —, branching of compound sporophore, 51. —, formation of spores, 63. —, gelatinousmembranes, 12. —, structure ofsporophore, 58. Calosphaeria biformis, 239. —, number of spores, 79. — princeps, 241. — verrucosa, number of spores, 79. Calothrix in Lichen-thallus, 398. . *. . Calycieae (Calyciei), dis- charge of spores, 96, 98. Canker in deciduous trees, 383. Cantharellus, 288, 297. — infundibuliformis, deve- lopment of sporophore, 56. Cap-fungi, 287. Capacity of germination, 343. — in Bacteria, 476. — in Mycetozoa, 448. Capillitium, 194, 310, 314. — in Mycetozoa, 431, 436. Capitate Bacteria, 461. Carbon dioxide, assimilation by Bacteria, 479. Caries in teeth, 472. Carpogonia, 212. Carpospores, 129, 232, 340. Catopyrenium, structure of thallus, 406. Cauloglossum, 319. — transversarium, 310. Celidieae (Celidiei), 416. Cell-forms in Bacteria, 458. Cell-membrane, 8. —, gelatinous, 9. — in Bacteria, 456. —, lignified, 9. —, mucilaginous, 9. —, sclerosed, 9. —, suberised, 9. Cell-nucleus, 6. — in Bacteria, 456. — in Mycetozoa, 425. Cellulose in Bacteria, 457. —inMycetozoa,428,441,442. Cellulose-membrane, 8. Cellulose-reaction, 13. Cementation of hyphae, 4. Cenangium Frangulae, 243. — fuliginosum, spores, 99. Cephalodia, 410. Cephalosporium, 334. Cephalotheca tabulata, dis- charge of spores, 97. Cephalothecium, 252. Ceratieae (Ceratiei), 427,434, 448. Ceratium hydnoides, deve- lopment of sporophores, 432*, 433*. — porioides, development of sporophores, 433, 433*. Ceratonema, 29. Cetraria islandica, chemical properties, 408. — —, colouring matter, 408. — —, Lichen-starch, ro. ——, structure of thallus, 404, &c. — straminea, incrustations, 408, Chaetocladieae (Chaetocla- diei), 148, 151. Chaetocladium, 117,147,149, 150, 151, 152, 153, 155. —, conditions of germina- tion, 350. — Fresenii, 150. — Jonesii, 150. — —, haustoria, 20. —, parasitism, 360, 385. Chaetomieae (Chaetomiei), 260. Chaetomium, 192, 211, 243, 260. —, discharge of spores, 97. — fimeti, 193. — —, discharge of spores, 97. —, germination, 111. —, hairs, 59. —, resin-excretion, ro. Chaetostylum, 152. Chain-gemmae, 155. Chalara, 267. — Mycoderma, 267. Chalara-form, 250. Change of host, 387. Cheilaria, 252. Chiodecton _nigrocinctum, structure of thallus, 411. Chionyphe Carteri, 379. Chlamydospores,1 5 4,249,336. Chlorangium Jussuffii, cal- cium oxalate, 409. Chlorophyll, 6. — in Bacteria, 455, 462, 474. Chlorosplenium aerugino- sum, colouring matter, 14. Choanephora, 150, 153, 154. Cholera in fowls, 472,-486. Chondrioderma, 448. — difforme, 423, 427, 433, 441, 452. — floriforme, 440. —,germinationand formation of plasmodia, 423*, 425*. Chromidia, 417. Chroococcaceae, 474. 423, Chroococcaceae in Lichen- thallus, 398. Chroolepus in Lichen-thal- lus, 397. — umbrinum, 398*. Chrysochytrium, 167. Chrysomyxa, 277, 282, 338. — Abietis, 284. —, abscision of spores, 69. —, capacity of germination, 344, 349- —, formation of spores, 66. — Ledi, 284. ; — —, parasitism, 388. — Rhododendri, 284. — —,abscision of spores,71*. — —, germination, teleuto- spore-layer, 284 *. — —, parasitism, 388. — —, spore-chain, 279*. ——, structure of spores, 101*, —., structure of spores, 1o1*, Chytridieae (Chytridiei),132, 160, 445,475. —, capacity of germination, 344. —, discharge of spores, 82. —, doubtful species, 170. —, parasitism, 360, 363, 364, 365, 386, 395. —, restingstateof spores, 344. —, swarm-spores, 107. —, thallus, 5. Chytridium Brassicae, 162. — macrosporum, 161. — Mastigotrichis, 161, — Olla, 161, 162. — —, propagation, 165 *. — roseum, 161. — vorax, 161, — —, swarmi-spores, 107. Cicinnobolus, 247, 252, 253. — Cesatii, pycnidia, 247%. Cilia, 107, 457. Circinella, 152. Cladochytrieae (Cladochy- triei), 165, 169. Cladochytrium, 170, 184. — Iridis, propagation, 166*. — —, swarm-spores, 108*., —, formation of spores, 61. —, germination, 109. — Menyanthidis, 166. Cladonia, 200, 222. —, cellulose, 13. — decorticata, 222. — furcata, Algae of the thal- lus, 397*, 404. — Novae Angliae, spermatia, ari”: — Papillaria, 221, 222. —, podetia, 402, — pyxidata, 222. INDEX. Cladiona rangiferina, 222, —-—, structure of thallus, 404. —, structure of thallus, 404, 406, Cladosporium, 252. — dendriticum, parasitism, 393, 394. —, formation of gonidia, 67. — herbarum, 229. —, spores, 68. Cladothrix, 457, 458, 459, 469, 472. Clamp-cells, 3. Clamp-connections, 2. Clathrocystis, 472. Clathrus, 322. — cancellatus, 312, 324. — —, compound sporo- phores, 324. — hirudinosus, 312. —, mycelial strands, 23. Clavaria, branching of com- pound sporophore, 51. —,compound sporophores,48. —juncea, cellulose-mem- brane, 8. — minor, sclerotium, 42. Clavarieae (Clavariei), 288, 303. —, structure of compound sporophore, 58. Claviceps, 186, 191, 192, 200, 235,239,244,246, 248, 260, —, cellulose, 13. —, fatty matter, 7. —, formation of gonidia, 65. —, gonidiophores, 36. —, inception of sporophore, 49. —, lipoxeny, 388. — microcephala tium), 41. — nigricans (sclerotium), 41. —, parasitism, 362. — purpurea, 220. — —, development of sporo- phore, 227*, 228*. — —, germination of sclero- tia, 38, 38*. — —, parasitism, 359. — —, sclerotia, 36*, 41. — pusilla, sclerotia, 41. —, resting state, 37. —, sclerotia, 30, 31, 33, 35, 36*, 39. —, secondary mycelium, 45. —y Spores, 99. —, structure of ascus, 95. Cleistocarpous Ascomycetes, 186, 193. Clitocybe, 297. Clostridium, 458, 460. — butyricum, 455, 461. (sclero- 507 Club-shaped Hymenomy- cetes, 287. Coalescence of hyphae, 2. Cocci, 458. Coccobacteria septica, 473. Coccocarpia molybdaea, Algae of thallus, 409. Coemansia, 156. Coenogonium confervoides, structure of thallus, 411. — Linkii, structure of thal- lus, 410*, 411. Coleosporium, 281, 282, 338. —, abscision of spores, 69. — Campanularum, 282. —, capacity of germination, 345. — formation of spores, 66. —Senecionis, parasitism, 388. Collema, 198, 212, 224, 231, 237, 239, 240, 241. —cheileum, number of spores, 79. — microphyllum, fertilisa- tion, 212*. — —, development of sporo- phore, 214*. —, soredia, 415. —, structure of thallus, 412, Collemaceae (Collemacei), 211,214, 231,234,258, 402. —, structure of thallus, 44. Collenchyma, 316, 328. Collybia, 297. Colouring matters, 14. — of Bacteria, 455, 457. — of fatty substances, 7, — of Lichens, 408. — of Mycetozoa, 424, 434. Colpodella, 447. Columella, 152,173, 435,438. Colus, 312. — hirudinosus, 325. — —, receptacle, 326*. Comatricha, 438. Commencement of fructifi- cation (archicarp), 121. Companion-hyphae, 215. Completoria, abjection of spores, 73. — complens, 160. —, parasitism, 363, 364, 393. Compound sporophore, 46, 48, 186, 288. —, development, 49. — in Ustilagineae, 178, 181, 184. —, structure, 57. Concrescence of hyphae, 4. Conditions of vegetation, general, 352. Confervae in Lichen-thallus, 397. Conidia, 129, 141. 508 Conidiobolus 160. Conidium, 131. Conjugation in Ascomycetes, 198. — in Ustilagineae, 178, 181, 184. — in Zygomycetes, 145. Conjugation-cells, 145, 148. Conoplea, 252. Conversion of membranes into mucilage, 9. — in abscision of spores, 69. — in Bacteria, 456. Coprinus, 291, 295, 296, 303, 304, 305, 306, 329, 330,331. —, abjection of spores, 73. —., abjunction of spores, 64. —, cementation of hyphae, 4. —, clamp-connections, 2. — comatus, 306. —, compound sporophores, utriculosus, 49. —,conditions of germination, 350. —, duration of growth, 51. — ephemeroides, 291, 295, 297, 332. — ephemerus, 297, 303. —, germination, 111. —, germ-pore, ror. —, growth of compound spo- rophore, 50. — lagopus, 291, 295,296,332. — —, gonidia, 332*. — micaceus, 295, 304, 306. — —, development of sporo- phore, 292*. — —, hymenium, 303*. —, mode of life, 357. — niveus, sclerotia, 42. —, secondary mycelium, 45. — stercorarius,295, 329, 332. — —, abjection of spores, 73. —, capacity of germination, 344. — —, germination of sclero- tia, 38, 39, 42. — —, sclerotia, 30, 32, 34, 35, 38, 39, 42. Coprolepeae, structure of spores, 102. Cora Pavonia, structure of thallus, 414. Corallofungus, 29. Cordyceps, 186, 191, 229. — capitata, 221. — cinerea, parasitism, 359. —, ejection of spores, 96. —, formation of gonidia, 66. —, growth of compound sporophores, 50, — militaris, 94, 221, 253, 255, 367. INDEX, Cordyceps militaris, germi- nation of gonidia, 371*. — —, parasitism, 359, 362, 367, 371. — ophioglossoides, 221. —, parasitism, 362, 367, 371. —, secretion of ferment, 355. — sphecocephala, 367. —, structure of ascus, 95. Coremium, 48. Cortex, 193. Cortical layer of compound sporophore, 58. Corticium, 287, 304. — amorphum, 302. — —, chemical behaviour of spore-membranes, 105. — —, formation of spores, 64*, — —, maturity of spores,68. —w—, structure of spores, 100, 101. —calcareum, secretion of calcium, 11. — calceum, spores, 64. — dubium, 335. — quercinum, 307. — —, periodical growth, 57. Cortina (curtain), 291. Coryneum, 252. —, spores, 68. Course of development in Fungi, 118. ; -—— in Bacteria, 459. Craterium, 434. Crenothrix, 457, 458, 459, 476. — Kiihniana, 469, 470*. Crepidotus, 333. Cribraria, 434, 435, 436. Cribrarieae (Cribrariei), 427, 448. —, experiments in germina- tion, 421. Cronartium, 280. —, capacity of germination, 345. —, parasitism, 388. Crucibulum, 311, 320, 321, 330. — vulgare, 319. — —, conditions of germina- tion, 350. — —, development of sporo- phore, 319*, 320*. — —, membranes, 12. Crustaceous Lichens, 402. —, growth in thickness, 407. Cryptospora, number of spores, 79. — suffusa, 239. Crystalloids, 7. Ctenomyces, 206, formation of Cucurbitaria, 221, 245. — elongata, 247, 248. — Laburni, 246, 248, 259. — —, development ofspores, 78. — —, ejection of spores, 95. — —, germination, 114. — macrospora, 246. — —, germination, 114. — —, layer of gonidia, 246*, Cutis, 58. Cyathus, 311, 320, 321, 329. —, clamp-connections, 2. — striatus, 321. Cyclomyces, 288, Cylinder-gonidia, 371. Cylindrosporium, 252. Cyphella, 287. Cyphellae, 407. Cystidia, 303. Cystococcus in thallus, 397, 398*. — viridis, 397*. Cystocoleus, 411. - —ebeneus, structure of thallus, 410*. Cystopus, 138, 233. —, abscision of gonidia, 66*, 69*. i — Bliti, parasitism, 391. — candidus, 135, 138. — —, capacity of germina- tion, 343. — —, conditions of germi- nation, 349. — —, fertilisation, 136*. —-—, germination, 136%, 138*, — —, gonidia, 138*. — —, haustoria, 20*. — —, parasitism, 389, 391. —cubicus, abscision of gonidia, 69. —, development, 134. —, endogenous formation of spores, 73. —, layer of gonidia, 48. —, parasitism, 363, 386. — Portulacae, abscision of gonidia, 66*, 69*. ——, capacity of germina- tion, 349. — —, parasitism, 358. — —, ripeness of spores, 68. —, structure of spores, 106, 107. —, Swarm-spores, 107, Cysts, 427. —, thick-walled, 427. Cytispora, 252. Cytisporeae(Cytisporei),251. Cyttaria, gelatinous mem- branes, 9, 13. Cyttarieae (Cyttariei), 186. Lichen- Dacryomitra, 288, 305. Dacryomyces, 288, 305, 306, 329, 331. — deliquescens, 331. ‘—, formation of spores, 63, 64. —, gelatinousmembranes, 13. Dactylium, 249. —, formation of spores, 65*. — macrosporum, coloration of membrane, 8. —, pits, 13. Dactylococcus in Lichen- thallus, 397. Daedalea, 288. —, hyphal weft, 3. —, membranes, 12. —, mycelial membranes, 22. — quercina, cellulose, 8, 13. —, suberisation of mem- branes, 9. Delastria, 195. Dematieae (Dematiei),mem- brane, 12. —, spores, 68. Dematium, 29. —, germination, 114. —herbarum, formation of gonidia, 67. — pullulans, sprouting, 271*. Dendryphium, 252. Dermatea amoena, 243. — carpinea, 243. — Coryli, 243. — dissepta, 243. Dermatocarpon, 192. Desertion of host (lipoxeny), 388. Diachea, 434, 436. — elegans, 424. Diatrype, 186, 192, 218, 240. —, number of spores, 79. — quercina, spermogonia, 241*, — —, number of spores, 79. — verrucaeformis, number of spores, 79. Dictydium, 427, 431, 435. Dictyonema, structure of thallus, 414. Dictyostelium, 442, 451. Dictyuchus, 143. — clavatus, 144. — —, formation of spores,75. —, formation of spores, 74. — monosporus, formation of spores, 75. —, swarm-spores, 108. Diderma, 434, 436. Didymium, 430, 436, 441, 448. — difforme, 427, 428, 429. — farinaceum, 436. — leucopus,423,424,428,436. INDEX. Didymium leucopus, plasmo- dium, 425*. — —, sporangium, 434*. — Libertianum, 423, 441. — nigripes, 436. — physaroides, 436. — Ppraecox, 423, 424, 427. — Serpula, 424, 425, 428, 429, 430, 434, 436, 452. —squamulosum, sporan- gium, 434*. Dimargariscrystalligena,156. Diplodia, 247. —, germination, 111. —, secretion of resin, 10. Discocarp, 187. Discomycetes, 186, 187, 189. —, as Lichen-fungi, 396. —, ejection of spores, 85, 86, 89. —, glycogen, 6. —, puffing of spores, go. Discus, 187. Diseases in silk-worms, 486, 489. Dispira cornuta, 156. Dissepiment, 301. Doassansia, 173. Dothidea, 191. — Melanops, 246. — Ribesia, germination, 114. —Sambuci, number of spores, 79. — Zollingeri, 245. Effect of parasite on host, 367. Ejection of spores, 84. Elaphomyces, 193. —, asci, 77. —, conditions of germina- tion, 352. —, discharge of spores, 81,97. — granulatus, 193. — —,development of spores, 80. —, mycelial strands, 22, 23. —, number of spores, 79. Empusa, 158. —-, abjection of spores, 73. — Grylli, 159. — macrospora, 158. — Muscae, 158, 159. Encarpium, 17. Enchylium, structure of thallus, 413. Endocarpon, 192. — miniatum, 222. — monstrosum, calcium ox- alate, 409. — pusillum, 224, 409. — —, Algae of thallus, 409. — —~, formation of thallus, 400, 5°9 Endocarpon pusillum, germ- ination, 339*. — —, hymenial Algae, 400, 401. —-—,number of spores, 79+ ——, structure of thallus, 406. Endomyces, 341. — decipiens, -266. Endophyllum, 278, 281, 285. — Euphorbiae, 281. ——-, parasitism, 364, 368, _ 390. — Sempervivi, 277, 281. — —, germination, 279*. — —, parasitism, 390. Endophytes, 360. —, behaviour to the living cell, 393. Endopyrenium, structure of thallus, 404. Endosporium, roo. Enerthenema, 438. Entomophthora, 158. —, abjection of spores, 73. — curvispora, 158, 159. —, formation of spores, 62. — ovispora, 158, 159. —, ‘ pleomorphism,’ 126. — radicans, 158, 159. Entomophthoreae (Entomo- phthorei), 132, 158, 184. —, parasitism, 362, 367, 371. Entyloma, 172, 173, 174,178, 179, 180, 181. — Calendulae, germination, 175*. — —, parasitism, 389. —, formation of spores, 61. — Magnusii, 179. —, parasitism, 362. — Ranunculi, 179, 180. — serotinum, 180. — Ungerianum, tion, 175*. Envelope-apparatus in As- comycetes, 186. Envelope of plasmodia of Mycetozoa, 426. Ephebe pubescens, 242. —-—, structure of thallus, 412*, — structure of thallus, 412. Epichloe, 186, 191, 192, 200, 221, 244, 246, 260, —, abscision of gonidia, 71. —, structure of sporophore, germina- 57- —typhina, formation of gonidia, 65. — —, parasitism, 359, 386, 399, 391. — —, structure of ascus, 95. 510 Epinasty of pileus in Agari- cineae, 50, 289. Epiphragm, 320. Epiphytes, 360. Epiplasm, 77. Episporium, 100, Eremascus, 187, 232, 233, 234, 236, 237. — albus, 197, 224. —, development of ascus, 198*, Ergot, 35. Erysipelas, 486. Erysiphe, 202, 232, 236, 238, 239; 245, 352. — Aceris, parasitism, 394. —, asci, 76. — communis, conditions of germination, 352. —, discharge of spores, 86, — Galeopsidis, 203. ——, conditions of germina- tion, 352. — graminis, 203. — —, conditions of germina- tion, 352. i — —, haustoria, 19. — guttata, number of spores, 79. — —, parasitism, 359, 394. —, hairs, 59. —, number of spores, 79. —, parasitism, 359, 363. — spiralis, 225. — Tuckeri, haustoria, 19*. Erysipheae (Erysiphei), 193, 198, 199, 201, 225,235,244. —, conditions of germination, 350. —, discharge of spores, 85. —, formation of gonidia, 66. —, haustoria, 19*. —, mycelium, 19*. —, parasitism, 386, 393. Euchytridieae (Euchytridei), 164. . Eurotium, 193, 198, 204, 226, 232, 234, 236, 237, 239, 245. —, abscision of gonidia, 70. —, asci, 76. — Aspergillus glaucus, con- ditions of vegetation, 353. — —, formation of gonidia, 70*, — —, parasitism, 369. —, capacity of germination, 348. —, compound sporophores, 49- —, discharge of spores, 81, 97, 98. — —, formation of spores, 62, —, parasitism, 369. INDEX, Eurotium repens, conditions of vegetation, 353. — —, development of sporo- phore, 203*. — —, parasitism, 369. —, resinous excretion, ro. —, simple sporophores, 46. —, structure of spores, 100. —, taking up of colouring matter, 14. Eusynchytrium, 167. Eutypa, 191, 218. —, discharge of spores, 97. Evernia flavicans, 406. — furfuracea, colouring mat- ter, 408. — —, structure of thallus, 406. —, soredia, 415. —, structure of thallus, 404. — vulpina, incrustations,408. ——,, structure of thallus, 408. Excipulum, 188. Exidia, 287, 305. —, gelatinous membranes, 3. — recisa, 337. — spiculosa, basidia, 305*. — —, formation of spores, 62*, Exoascus, 265, 266. — alnitorquus, 265, 266, — aureus, 265. — bullatus, 266. — deformans, 265. —, ejection of spores, 89. — epiphyllus, 266. —, germination, 114, 115. —, number of spores, 79. —, parasitism, 368, 386, 390, 393. — Populi, 266. — Pruni, 265, 266. — —,development of spores, 79- ——, ejectionofspores,86,92. ——, inception of sporo- phore, 49. — —, parasitism, 393. —, structure of spores, 100, — Ulmi, 266. Exoascus-group, 269. Exobasidium, 271, 287, 329, 331, 368. — Lauri, parasitism, 368. —, parasitism, 386. — Vaccinii, parasitism, 362, 368. Exosporium, 100, 135, 252. —, spores, 68. — Tiliae, germination, 114. Fatty matters, 7. Favolus, 288, Favus, 376. Feeder (host), 358. Felted tissue, 5. Ferment, secretion, 355, 452. Fermentation caused by Bac- teria, 481. — — by Fungi, 384. Ferns, course of develop- ment, 120. Fertilisation-tube, 134. Fibrillaria, 29. Filamentous Fungi, 1. Filamentous sporophore, 46. Fistulina, 302. — hepatica, 300, 302, 334. Flacherie (in silk-worms), 486, 489. Flagella, 107, 422, 457. Flagellatae, 445, 475. Flower of tan, 431. Flowering plants, course of development, 121, Flowers of wine, 267, 358. Foliaceous Lichens, 401. Food, a condition of ger- mination, 351. Food-material of Fungi, 353. Form-genera, 119, 459, 473. Form-species, 119, 459, 473. Fowl-cholera, 472, 486. Frill (in Hymenomycetes). See Armilla. Frog-spawn 469. Fructification, 120. Fruticose Lichens, 401, Fuligo, 423, 424, 425, 428, 429, 431, 440, 448, 449, 450, 452. — varians, 424, 439, 441. Fumago, 245, 247, 249, 251, 253, 254, 271. —, formation of gonidia, 66, — salicina, 244. Fungi, affinities, 337, 340. —, course of development, 118. —, genealogy, 337, 340. Fungus-body, 2. —, compound, 2. —, sclerotioid, 190. —, slimy mucilaginous, 9. Fungus-cellulose, 8, 13. Funiculus, 321. Fusarium heterosporum, re- sistance of spores, 346. Fusiform rods in Bacteria, 458. Fusisporium, 249, 252. — Solani, 245. —, spores, 68. (Bacterium), Galls, 369. Gametes, 120, 148, 150, Gastromycetes, 286, 308, 337. Gastromycetes, compound sporophores, 49. — conditions of germination, 352. —, development of sporo- phore, 50. —, formation of spores, 63*. —, gelatinous membranes, 9. —, membranes, 11, 12. —, structure of sporophore, 58. Gattine, 488. Gautieria, 308, 337. Geaster, 308, 309, 311, 315, 316,317. —, capillitium, 12. — coliformis, 314. — —, capillitium - threads, 314*. — fimbriatus, 314, 316, 317. — fornicatus, 314, 316, 317. — hygrometricus, 308, 309, 313, 315, 316, 317. — —, compound phores, 316*. — —, formation of spores, 63*. — —,gelatinous membranes, 9, 12. — mammosus, 314, 317. — rufescens, 317. — tunicatus, 309. Gelatinisation of membranes, sporo- 9. — in abscision of spores, 69. — in Bacteria, 456. Geminella Delastrina, 174. Gemmae, 60, 61, 154, 155, 230, 328, 330, 331. Gemmae-cups (in Lichens), 407. Genabea, 195, 196. Genea, 196. —, mycelial strands, 22. —, structure of spores, roo. Genealogy of Fungi, 337,340. Geoglossum, 189. —, development of spores, 78. —, ejection of spores, 86. —, hirsutum, development of spores, 78. Germ-pore in Mycetozoa, 441. Germ-pores, 100, IIT. Germ-tube, 1, 110. Germination, 109, 130. — in Bacteria, 462, 465, 467. — in Mycetozoa, 448. —, conditions of, 349. — — in Bacteria, 462, 477. — — in Mycetozoa, 448. — phenomena of, 343. INDEX. Germination of spores, 109. Gleba, 193, 309. Gloeocapsa in Lichen-thal- lus, 397*, 398. Gloeosporium, 252. Glycogen, 6, 77. Gnesiolichenes, 402. Gomphidius, 297. Gonatobotrys, 252. —, formation of 63. —, gonidia, 98. —, simple sporophores, 47. Gonidia, 45, 60, 129, 131, 179, 180, 239, 244, 331, 334, 338, 340. —, accessory, 146. —, capacity of germination, 343+ — in Lichens, 417. Gonidial layer layer), 417. Gonidiophore, 45, 245. Gonionema, structure of thallus, 412. Gonoplasm, 134. Granulose in Bacteria, 455, 461. Graphideae (Graphidei), origin of thallus, 399. —, soredia, 415. —, structure of thallus, 410. — subcortical thallus, 402. Graphiola, 173. Graphis scripta, origin of thallus, 399. — —, Algae of thallus, 398*. spores, (gonimic — —, structure of thallus, 410. Graphium, 29. Green rot in wood, 14. Growth of parasites, 367. — of Fungus-bodies, 3, 50. Guepinia, 287, 305. —contorta, structure of sporophore, 58. —, gelatinous membranes, 3. — helvelloides, 287. Guttulina, 443. — protea, 442, 443. Guttulinae, 442. Gymnoascus, 198, 199, 206, 224, 232, 235. Gymnomycetes, 251, 252. Gymnosporangium, 279. —, parasitism, 388. — Sabinae, 276. Gyrocephalus, 287. Gyrophora, 189. — cylindrica, spermogonium, 240. Haematomma _ ventosum, structure of thallus, 405. 511 Hairs of compound sporo- phores, 59. Haplocystis mirabilis, 170. Haplomycetes, 252. —, thallus, 1. Haplotrichum, 252. —-, formation of spores,62,6 3. —, simple sporophores, 47. Haustoria, 18, 19*. Hay-bacillus, 467. Helicosporangium, 263. Helicostylum, 152. ‘Heliotropism in plasmodia, 449. Helminthosporium, 252. —, spores, 68. Helotium, ejection of spores, 86. Helvella, 189. — crispa, ejection of spores, 86 — —, puffing of spores, 92. —-—, structure of sporo- phore, 58. — elastica, development of spores, 77. —-—, structure of sporo- phore, 58. — —,structure of spores,106. — esculenta, development of spores, 77. — —, germination, 113*. —-—, structure of sporo- phore, 58. —-—,, structure of spores, 106. —, structure of sporophore, 57- Hemiarcyria, 437, 440. — clavata, 437. — rubiformis, 437, 438, 440. Hemileia, 274. —, capacity of germination, 345. — vastatrix, 282. — —, parasitism, 388. Hemipuccinia, 279. Hendersonia, 252. Himantia, 29. Homologies of stages of de- velopment, 119. — restored, 123. — interrupted, 123. Host (vegetable and animal), 358. —, reaction on parasite, 366, Hyacinth, yellow sickness, 482. Hydneae, 288, 303, 333. Hydnobolites, 195. Hydnocystis, 196. Hydnotria, 196. Hydnum auriscalpium, hairs, 59- 512 Hydnum cirrhatum, 301. — diversidens, 307. — —, parasitism, 384+ — Erinaceus, 335. — —, gelatinous membranes, 9. — gelatinosum, 301. — zonatum, 301. Hydrotropism in plasmodia, 449, 450. Hymenial Algae, 400, 401. Hymenial gonidia, 417. Hymenium, 49, 191, 300. Hymenochaete, 303. Hymenogaster, 308. — —, clamp-connections, 2. — —, formation of spores, 63. — Klotzschii, 309, 313. — —,, formation ofspores,63. — —, germ-pores, ror. Hymenogastreae (Hymeno- gastrei), 308, 309, 310, 313, 337- y —, conditions of germina- tion, 352. —, formation of spores, 63. —, mycelial strands, 22, 23. Hymenomycetes, 286, 287, 337. —., abjection of spores, 73. — as forming Lichens, 396, 414. —, capacity of germination, 343- —, compound sporophores, 48. —, ferment-secretions, 355. —., formation of spores, 63. —, gelatinous membranes, 9, 12. —, glycogen, 6. —, growth of compound sporophores, 51, 55. — —, periodic, 51. —, gymnocarpous, 289, 296. —-, membranes, 12. —, mycelial membranes, 21, 22. —, parasitism, 384. —, sclerotia, 32. —, structure of spores, 106, —, veiled, 289, 296. Hymenophorum, 300. Hypertrophy, 368. Hypha (proper name), 29. Hypha, 1. —, Woronin’s, 199, 218. Hyphae, ascogenous, 186, 208, 214. —, cementation, 4. —, coalescence, 2. —, concrescence, 4. Hyphal weft, 3. INDEX. Hyphasma, 29. Hypholoma, 197. Hyphomycetes, 251. —, abscision of spores, 71. —, absence of calcium, 11. —, thallus, 1. Hypochnus, 287. — centrifugus, basidia, 301*. — —, gonidial layer, 48. — —, sclerotia, 32, 40, 42. —, clamp-connections, 2. —, mycelial membranes, 22. — purpureus, 306. Hypocopra, 198, 210. — finicola, 210, 224, 261. —, structure of spores, 102. Hypocrea citrina, number of spores, 79. —, formation of gonidia, 65. — gelatinosa, number of spores, 79. — lenta, number of spores, 79- — rufa, 253. —, number of spores, 79. Hypodermii, 184. Hypomyces, 245,249, 254. — armeniacus, sclerotia, 41. — asterophorus, 336. — Baryanus, 336. —, capacity of germination, 345+ — chrysospermus, 249. —, detachment of spores, 68. —, formation of gonidia, 65. — rosellus, 249. — Solani, 246, 249. Hyponasty of pilei of Agari- cineae, 56, 289. Hypothallus, 405. Hypothecium, 188. Hypoxylon,186,218,244,248. —concentricum, discharge of spores, 104. Hysterangium, 308, 310. —clathroides, gelatinous membranes, 12. — gelatinous membranes, 9. Hysterineae (Hysterinei), 190. —, parasitism, 386. —, structure of spores,1o2. Hysterium macrosporum, gelatinous membranes, 9. — nervisequum, structure of spores, 102. Ileodictyon, 312. Imbricaria caperata, incrus- tations, 408. — incurva, 408, — saxatilis, 246. — sinuosa, 246, incrustations, Imbricaria soredia, 415. — tiliacea, Algae of thallus, 398*, Incipient mycelium, 178. Incrustations of Lichens, 408. Inner membrane of spores, 100, Interstitial substance in spo- rangium of Mucorini, 75. Intralamellar tissue, 301. Invertin, 355. Involucrum, 289. Involution-forms, 458. Irpex, 288. Isaria, 48, 273. — brachiata, branching, 51. —, capacity of germination, 344. — farinosa, 255. — —, parasitism, 362. — strigosa, 253. Isidium, 406. Kickxella, 156. Kneiffia, 287. Laboulbenia Baeri, parasi- tism, 359. — flagellata, 263*. — Nebriae, 264. — vulgaris, 264. Laboulbenieae niei), 263. —, parasitism, 360, 365, 367, (Laboulbe- 370. —, thallus, 5. Lactarius, 298, 304. — chrysorrhoeus, 298, 301. — deliciosus, 298, 303, 304. — mitissimus, 298, 302. — pallidus, 298. —, pseudo-parenchyma, 3. — subdulcis, 301. ——, structure of sporo- phore, 299*. Lagenidium, 139. Lamellae, 288. Lamia culicis, 159. Lamina proligera, 187. Lamina sporigera, 187. Lateral branches in Sapro- legnieae, 141. Laticiferous tubes, 299. Laudatea,_ structure’ of thallus, 414. Layer (stroma, receptacu- lum), 48. Lecanactis illecebrosa, Al- gae of thallus, 398*. ——, structure of thallus, 41l. Lecanora, 223. 299, 301, Lecanora pallida, develop- ment of spores, 78. — —, thallus, 400, 402, 405. — subfusca, apothecium, 190*, — Villarsii, structure of thallus, 405. Lecidea, 223. — confervoides, structure of thallus, 405. — enteroleuca, structure of thallus, 405. — formosa, 222. — geographica, structure of thallus, 405. — parasema, thallus, 405. — sabuletorum, 245. Lecidella enteroleuca, de- velopment of spores, 78. —-—,growth of thallus, 404%. Lempholemma, structure of thallus, 412. Lenzites, 288, 301. — betulina, membranes, 12. —, growth of compound sporophores, 57. Leocarpus vernicosus, 424, 434. Leotia, 189. — lubrica, development of spores, 78. Lepiota procera, 297. Leptochrysomyxa, 283. — Abietis, 338. —, capacity of germination, 345+ Leptogium, 198. —, structure of thallus, 412, structure of 413. Leptomitus brachynema,1 44. — lacteus, 144. —, formation of spores, 74. Leptopuccinia, 283, 344. — annularis, 283. —, capacity of germination, 344, 348. — Circaeae, 283. — Dianthi, 284. — —, parasitism, 361, 362. — Malvacearum, 284. — Veronicae, 283. Leptopuccinieae (Leptopuc- ciniei), 283, 338. Leptosphaeria Doliolum, 247. Leptothrix, 458, 459. — buccalis, 456, 472. Leptothyrium, 252. Lesions in spores, effect on capacity of germination, 346. Leucochytrium, 167. [4] INDEX. Leuconostoc mesenterioides, 457, 469. Libertella, 252. Licea, 435, 436. — flexuosa, 434, 435, 441. — pannorum, 423, 441. — Serpula, 441. Lichen-acids, 10, 408. Lichen-fungi, 188, 224, 242. —, conditions of germina- tion, 350. —, ejection of spores, 93. —, gelatinous membranes, 9. —, mode of life, 395. —, parasitism, 360, 366, 367, 386. —, resistance of spores, 346. —, swelling of membrane, 9. Lichen-sporocarps, 222. Lichen-starch, 10, 408. Lichen-thallus, 59. —, chemical constitution, 407. —-, crustaceous, 401. —, epiphloeodic, 402. —, foliaceous, 401. —, fruticose, 401. —, growth, 4o1. —, heteromerous, 402. —, homoiomerous, 402. —, hypophloeodic, 402. —, mode of origination, 398. —, subcortical, 402. —, structure, 4o1. Lichens, 396. —, cell-membranes, 8. —, colouring matter, 408. —, ejection of spores, 87. —, historical remarks, 416. —, hyphal weft, 3. —, number of spores, 79. —, pseudo-parenchyma, 3. —, swelling of membrane, 9. —, thallus, 1. —, true, 402, Lichenaceae _ 402. Lichenin, 10, 407. Lichenosphaeria, structure of thallus, 412. Lichina, discharge of spores, 96. —, structure of thallus, 410. Lichinic acid, 408. (Lichenacei), Lignification of membranes, 9. Lindbladia, 431. Rpeseay (desertion ofhost), 388 Long rods (Bacilli), 458. Loss of capacity in sporo- phores of Ascomycetes, 254. Lycogala, 423, 427, 431, 449, 452. — epidendron, 440, 44. Ll 513 Lycoperdaceae (Lycoper- dacei), 308, 310, 311, 313, 337 —, experiments in germina~ tion, 352. —, mycelial strands, 22, 23, -—, pseudo-parenchynia, 3. Lycoperdon, 11, 308, 309, 310, 314, 315. —, abjunction of spores, 64. — Bovista, 314. — giganteum, 314. — perlatum, 316, —, pits, 13. — pyriforme, formation of spores, 63*. Lyngbya in Lichen-thallus, 398. Lysurus, 325. Macrococci, 458. Macrogonidia, 225. Macrosporium, 252. — Sarcinula, 229. Madura-disease, 379. Main series of Fungi, 120. Malignant oedema, 486. Mallotium = Hildebrandtii, structure of thallus, 413*. _, abe of thallus, 412, ental veil (in Hymeno- mycetes), 290. Martenselia, 156. Massaria, 192. — Platani, 258. —, structure of spores, ro2. Mechanism for abjection of cells, 72, 85. Medulla (Medullary layer) of*Lichen-thallus, 403. —of compound _ sporo- phores, 58. Megalogonidia, 225. Megalospora affinis, calcium oxalate, 409. — —, germination, 112*, —, number of spores, 79. — sanguinea, calcium oxa- late, 409. Melampsora, 281. — Géppertiana, parasitism, 388, 390, 391. — populina, 280, 282. — salicina, 282. Melanconis, II4. —, structure of spores, ro2. Melanconium, 252. —, spores, 68. Melanogaster, 309, 310. —, gelatinous membranes, 9, 13. Melanospora, 191, 192. germination, 514 Melanospora parasitica, 191, 198, 199, 210, 211, 226, 235, 251, 365. — —, discharge of spores, 97. — —, parasitism, 360, 365, 366, ——, structure of spores, 106, Melanotaenium, 176. Melogramma Bulliardii, ger- mination, 114. Membranes of vegetative cells, 11. Mentagra parasitica, 376. Merispores, 98. Merulius, 288, Mesentericae, 424. Metamorphosis, 256, 259. —, mycetogenetic, 368, Metoecious, 387. Metoecism, 388. Metoxenous, 387. Micrococcus, 459, 473. — Bombycis, 489. — prodigiosus, 455. — —, taking up of colouring matter, 14. Microcysts, 427. Microgonidia, 225. Microgonidium, 419. Micropuccinia, 285. Microsomata, 455. Microsporon Audouini, pa- rasitism, 376. — furfur, parasitism, 376. — Mentagrophytes, parasi- tism, 376. Milk, blue, 462. Mitremyces, 312, 326. —, gelatinous membranes, 9, 13. Mode of life of Bacteria, 476. — of Mycetozoa, 448. — of Fungi, 343. Monad-forms, 458. Monadopsis, 447. Monas Amyli, 447. Monoblepharis, 132, 140, I4I. —sphaerica, fertilisation, 140*, —, swarm-spores, 107, 109. Montagnites, 297. Morchella, 189. —, ejection of spores, 89. — esculenta, development of spores, 77. — —, ejection of spores, 85. —, structure of sporophore, 37+ Moriola, 416. Morioleae (Moriolei), 416. Mortierella, 146, 149, 150, 151, 154, 155. INDEX, Mortierella, spores, 83. —, haustoria, 20, — nigrescens, 150. — reticulata, resistance of spores, 346. — Rostafinskii, 150. — —, experiments in germi- nation, 352. Mosses, course of develop- ment, 120. Mother of-vinegar, 456, 458, 481. — -fungus, 472. Moulds, fatty matters, 7. Mucor, 149, 152, 155. —circinelloides, ferment- production, 358. —corymbifer, parasitism, 360. —, discharge of spores, 83. —, ferment-production, 358. —,formation of spores,7 4,75. — fusiger, 150, 152. — —, cellulose-membrane,8. ——, resistance of spores, discharge of 346. —, mode of life, 357. — Mucedo, 150, 154. — —, cellulose-membrane,8. — —, ferment - production, 358. er — —, germination, 113. —, parasitism, 380. — plasmaticus, formation of spores, 75. —, pleomorphism as alleged, 126, — racemosus, 150. — —, conditions of vegeta- tion, 354. — —, ferment - production, 358. oo — —, parasitism, 380. —, resistance of spores, 347. — rhizopodiformis, parasi- tism, 359, 360, 370. —, simple sporophores, 46. — spinosus, ferment - pro- duction, 358. — stolonifer, 147, 150, 152. ——, conditions of germi- nation, 350, 352. — —, conjugation, 148*, — —, ferment - production, 358. sya — —, germination, 113. -— —, parasitism, 380. — —, resistance of spores, 347- ——, secondary mycelium, 46. —, taking up of colsaring matter, 14. Mucor tenuis, 150. Mucor-yeast, 156. Mucoreae(Mucorei),148,151. Mucorin, 7. Mucorineae (Mucorini), 132, 145, 169, 232, 233, 236, 271. —, calcium oxalate, 11. —, capacity of germination, 348. —, cell-nucleus, 6. —, conditions of : germina- tion, 350. —, crystalloids, 7. —, doubtful, 156. —, ferment-secretion, 358. —, formation of spores, 75. —, gemmae, 60, 61. —, germination, 113. —, glycogen, 6. —, parasitism, 363, 385. —, resting-state of spores, 3446 —, simple sporophores, 46. —, thallus, 1. Muscardine, 374. Mushrooms,cell-membranes, 8. —, thallus, 1. Mutualism, 369. Mycelial membranes, 18, 21. Mycelial strands, 18, 22. Mycelium, 18. —, filamentous, 18. —, fibrillose, fibrous, 18, —, sclerotioid, 42. —, secondary, 45. Mycena, 297. —, cementation of hyphae, 4. —, gelatinous membranes, 9, 13- Mycenastrum, 315. — corium, 315. — —, capillitium - threads, 314%, Mycetozoa, 411. —., affinities, 442. —, doubtful, 446. Mycoderma, 22, — aceti, 481. Mycoderma-form, 250. Mycogone, 245, 252. Mycoidea__parasitica_in Lichen-thallus, 398. Mycoprotein, 457. Mycosis, 369, 379. Mycothrix, 458. Myelin, 300. Mylitta, 42. Myriangium, 193, 416. — Durieui, 197. Myriocephalum botryospo- rum, structure of spores, 103, Mystrosporium, 229, 252. Myxamoebae, 423. Myxastrum radians, 447. M yxocyclus, 252. — confluens, structure of spores, 102, Myxogasteres, 421. Myxomycetes, 421, 475. —., affinities, 442. Myzocytium globosum, 139. Naemaspora, 252. Naetrocymbe, 416. Neck in perithecia, 191. Nectria, 200, 215, 221, 239, 245. , — cinnabarina, 244, 246. — —, parasitism, 362, 383. — cucurbitula, parasitism, 383. — development of spores, 78. —, discharge of spores, 97. — ditissima, 228. — —, parasitism, 383. —, germination, 114, 115. — inaurata, 114, 115. — Lamyi, germination, 115. — Solani, 246, — —, abscision of gonidia, 71. Nephroma arcticum, Algae of thallus, 409. —, structure of thallus, 406. Nephromium, Algae of thallus, 409. New formation of members caused by Fungi, 368. Nidularia, 311, 320. Nidularieae (Nidulariei), 308, 312, 319, 332. —, gelatinous membranes, 13. —, mycelial strands, 22, 23. Nosema Bombycis, 488. Nostoc in Lichen-thallus, 397%, 398. Nostocaceae, 475. — in Lichen-thallus, 398. Nucleariae, 447. Nuclei in spores, 106. Nuclein, 6. Nucleus in perithecia, 193. Nummularia, 218. —, discharge of spores, 97. Nutritive adaptation, 356. Nyctalis, 297, 334, 341. — asterophora, 335, 341. —-—, compound _ sporo- phores, 335*. — mycrophylla, 336. — parasitica, 336. — —, development of sporo- phore, 55. INDEX, Obelidium, 164. Obryzum, structure’ of thallus, 412. Ochrolechia pallescens, cal- cium oxalate, 409. — —, germination, 112. —-—-, structure of thallus, 405. : — tartarea, calcium oxalate, 408. Octaviania, 308. — asterosperma, compound sporophores, 308*. -— —, hymenium, 309*. — carnea, 309, 313. — —, formation of spores, 63". —., structure of spores, 100, Oedema, malignant, 486. Oidium, 238, 252. — albicans, parasitism, 377. — aurantiacum, resistance of spores, 347. — erysiphoides, 252. — fructigenum, 252. — lactis, 252, 253, 377. — —, cell-nucleus, 6. — —, formation of spores, 67. — leucoconium, 252. — Tuckeri, 225. — —, parasitism, 387. Oil-drops in spores, 106. Olpidieae (Olpidiei), 166, 167, 168, 169, 170. Olpidiopsis, 444. — fusiformis, 166. —, parasitism, 393. — Saprolegniae, 161, 166. Omphalaria, structure of: thallus, 413. Omphalarieae (Omphalariei), structure of thallus, 413. Omphalia, 297. Onygena, 193. — corvina, 196. — —, conditions of germina- tion, 351. —, discharge of spores, 97. — equina, 197. — faginea, 335. Oogonia, 120, 133. Oosphere, 120, 133. Oospores, 129, 232. —, capacity of germination, 343. —, resting state, 344, 345. Opegrapha filicina, 397. —-—, structure of thallus, 41. —plocina, structure of thallus, 412. — saxatilis, structure of thallus, 411. Sis 515 Opegrapha varia, 246. — —, structure of thallus, 411. — vulgata, 246. Ophidomonas, 472. Organs, functionless in As- comycetes, 256. — of attachment, 45. — of propagation, 124. Ostiole of perithecium, rgr. Otomycosis aspergillina, 369. Outer envelope of ascocarp, 188, Oxygen as a condition of germination, 349. Ozonium, 29. Palmellaceae in Lichen- _ thallus, 397. Palmellae-forms in Bacteria, 459- Panhistophyton, 488. Pannaria, 223. —, structure of thallus, 410. Panus stypticus, structure of sporophore, 58. — —, gelatinous membrane, 13. Papulospora, 2. Paraphyses, 48, 76, 187, 192, 286, 302. — envelope, 275. Parasites, 356, 358, 481. —, autoecious, 387. —, autoxenous, 387. —., facultative, 356, 369. —, inhabiting animals, 369. -—-, inhabiting plants, 379. —, metaxenous, 387. —-, metoecious, 387. —, obligate, 356. — which change their host, 387. Parmelia, Algae of thallus, 409. — pulverulenta, 222. —, soredia, 415. — stellaris, 222. —, structure of thallus, 406. Paulia, discharge of spo es, 97- : —, structure of thallus, 413. Paxillus, 297. Pébrine, 488. Peccania, structure of thallus, 413. Pellicula (cutis), 58. Peltigera, 240. —, Algae of thallus, 409. — aphthosa, structure of thallus, 406. —canina, structure of thallus, 406. —, incrustations, 408. 516 Peltigera malacea, structure of thallus, 406. —, structure of thallus, 404, 406, Penicillium, 193, 198, 199, 226, 232, 234, 239, 245, 251, 254. —, abscision of gonidia, 66, 70*, — aureum, 206, —, capacity of germination, 348. —, conditions of germination, 350. —, conditions of vegetation, 353, 354+ —, discharge of spores, 81, 97- —, effect on substratum, 358. —, fatty matters, 7. —, formation of spores, 62. —, germination, 111, — glaucum, 204, 226. — -—,, abscision of gonidia, 70*, — —, capacity of germina- tion, 344. — —, cell-nucleus, 6. — —, conditions of germina- tion, 349. — —, mycelial membranes, 33. — —, parasitism, 370, 380. ——-, resistance of spores, 347+ —, gonidiophores, 48. —, sclerotioid compound sporophores, 43. —, secretion of ferment, 355. —, simple sporophores, 46, —, thallus, 1, Perichaena, 435. — liceoides, 423, 427, 428, 435, 441, 448. Periconia, 252. —, formation of spores, 66. Peridermium elatinum, 277, 282. — —, parasitism, 368, 388, 390. — Pini, parasitism, 388. — —, structure of spores, 100, Peridiola, 311, 320, Peridium, 48, 193, 308, —, inner, 311, —, outer, 311. Periphyses, 192, Periplasm, 133. Perithecia, 76, 187, 190, 239, 401. 275; INDEX, Peronospora, 138, 232. —, abscision of spores, 72. — Alsinearum, fertilisation, 133*. — arborescens, fertilisation, 133%, — Arenariae, parasitism,391. — calotheca, haustoria, 20*. — densa, germination, 112. — —, haustoria, 20. — —, parasitism, 393. —, development, 134. —, discharge of spores, 82. —, membrane, 12. — nivea, haustoria, 20. — —, parasitism, 363, 393. — parasitica, haustoria, 20. — —, parasitism, 359, 362. —, parasitism, 358, 386, 391. — pygmaea, germination, I1i2, — —, haustoria, 20. — —, parasitism, 364. — Radii, parasitism, 364, 390, 391. —, simple sporophores, 46, 47. —, thallus, 1. — Umbelliferarum, _parasi- tism, 363, 389. — Valerianellae, 135. — violacea, parasitism, 368, 390, 391. sl — viticola, parasitism, 393. Peronosporeae (Peronospo- rei), 132, 183, 232, 233, 236. —, absence of calcium, 11. —, capacity of germination, 343» 344) 349 —, cell-nucleus, 6. —, cellulose-membrane, 8. —, conditions of germina- tion, 350. — discharge of spores, 82. —, formation of spores, 74, 75+ —, germination, 113, —, haustoria, 20*. —, mycelium, 20*, —, parasitism, 359, 362, 386, 393. —, pleuroblastic, 20, —, resistance of spores, 345. —, resting state of spores, 344- . —, swarm-spores, ro9. —., thallus, 1. Pertusaria communis, ger- mination, 114*, — de Baryana, germination, 112*, — fallax, calcium oxalate, 409. 358, Pertusaria lejoplaca,develop- ment of spores, 78. — —, germination, 114*, —, number of spores, 79. —, soredia, 415. —, structure of thallus, 405. Peziza (see also Sclerotinia), 189. — abietina, 86. — —, ejection of spores, 86. ——, structure of spores, 106. — Acetabulum, develop- ment of spores, 106, — —, ejection of spores, 85. — —, puffing of spores, 89, 92. — —, structure of spores, 77. — aeruginosa, colouring mat- ter, 8. — Aglaospora, 243. — arduennensis, 243. — aurantia, fatty matters, Js —-—, structure of spores, Ioo, — baccarum, sclerotium, 30, 41. — benesuada, doubtful sper- matia, 243%. — bolaris, 243. — —, germination, 115. — calycina, development of spores, 78. — Candolleana, sclerotium, 30, 31, 32. — ciborioides, 30, 41. — confluens, 208. — —, development of spores, 76, 77*. — —, ejection of spores, 86. —convexula, ejection of spores, 85, 86. ——, structure of spores, 102, —cupularis, ejection of spores, 85, 86. — Curreyana, desertion of host, 388. — —-, sclerotia, 33, 37, 41. — Cylichnium, 243. — —, germination, 115. —, development of asco- spores, 76. : — Duriaei, sclerotia, 37. — Durieuana, 243. — —, desertion of host, 388. — —, sclerotia, 41. —, ejection of spores, 89. — Fuckeliana, 245, 254. — —,abscision of spores, 63, 72. — —, cell-nucleus, 6, sclerotium, Peziza Fuckeliana, develop- ment of spores, 62, 78. — —, doubtful spermatia, 243. — —, gonidiophores, 38. — —, resistance of gonidia, 347- — —, sclerotia, 31*, 37, 41. — fulgens,colouring matters, 8. , mycelial strands, 22. — fusarioides, 242. — granulata, 215. — -—, ejection of spores, 86. —, hairs, 59. — hemisphaerica, structure of spores, 58. ——, structure of sporo- phore, 106. —, inception of sporophore, 49. — melaena, development of spores, 77. — —, ejection of spores, 85, 86 — —, number of spores, 79. —-—, structure of spores, 102, 106, — melanoloma, 215. — nivea, development of sporophore, 53. —pitya, development of spores, 76. — —, ejection of spores, 85. — Rapulum,mycelial strands, 22. — ripensis, sclerotium, 41. — Sclerotiorum, 243. — —, clamp-connections,19. — —, compound sporo- phores, branching, 51. — —, development of spores, 78. — —, development of sporo- phore, 53*. — —, ejection of spores, 87*. — —, puffing of spores, 89. — —, sclerotia, 30, 31*, 35, 37, 41. — —, structure ofspores, 106. ——, structure of sporo- phore, 58. — scutellata, 215. —, structure of spores, 99. —, structure of sporophore, BOe.- — Tuba, sclerotia, 41. — tuberosa, 243. — —, development of spores, 78. — —, germination, 115. — —, sclerotia, 30. ——, structure of spores, 106. INDEX, Peziza_ vesiculosa, ejection of spores, 86. ——, structure of spores, 106, Phacidiaceae (Phacidiacei), 190. —, parasitism, 386. Phacidium, development of spores, 83. —, lipoxeny, 388. — Pinastri, development of spores, 83. Phalloideae (Phalloidei), 308, 309, 312, 322, 338, 340. —, compound sporophores, 49. — —, growth, 51. —, conditions of germina- tion, 352. —, formation of spores, 63. —, gelatinous membranes, 9, 13. —, mycelial strands, 22, 23. —, pseudo-parenchyma, 3. —, secretions of calcium, 11. Phallus, 312. — caninus, calcium oxalate, ar, — —, development of sporo- phore, 322, 323*. — —, formation of spores, - 63*. — —, mycelial strands, 23. — impudicus, development of sporophore, 322, 323*. — —, duration of growth,51. — —, mycelial strands, 23. Phellorinia, 327. Phelonites strobilina, 282. —, structure of spores, 100. Phlyctidieae (Phlyctidiei), 164. Pholiota, 297. Phoma, 248, 252. Phragmidium, 276, 277. —, detaching of spores, 68. —, parasitism, 393. —, spores, 68, 98. Phragmotrichum, spores, 68. Phycolichenes, 402. Phycomyces, 146, 147, 150, 152, 155. —, discharge of spores, 83. — microsporus, 150. — nitens, 150. — —, capacity of germina- tion, 344. — —, membrane, 8. — —, mycelium, 146*. — —, organs of propagation, 146*, —, resistance of spores, 346. Phycomycetes, 120, 132. —, formation of spores, 74. 517 Phycomycetes, swarm- spores, 107. Phyllachora, lipoxeny, 388. —, stroma, 43. — Ulmi, 216. — —, ejection of spores, 94. Phyllactidium in Lichen- thallus, 397. Phylliscum, structure of thallus, 413. Phyllosticta, 252. Phyllosticteae(Phyllostictei), 251. Physareae (Physarei), 424, 426, 428, 430, 433) 434, 4395 440; 441, 449, 451. Physarum, 430, 434,436, 448. — album, 441. — aureum, 435. - — hyalinum, 435. — leucophaeum, capillitium, sporangium, 435*. — macrocarpum, 448. — psittacinum, 424, 435- — sinuosum, 428. — sulphureum, 435. Physica parietina, Algae of thallus, 397*. — —, incrustations, 408. — —, soredia, 416. ——, structure of thallus, 403*, 406, Physma, 108, 214, 231, 240, 259. — chalazanum, thallus, 397*. —, structure of thallus, 412, 413. Physoderma Butomi, 166. — Heleocharidis, 166, — maculare, 166. — pulposum, 164. — vagans, 166. Phytophthora, 137. —, development, 134. Algae of —discharge of swarm- spores, 82*, —,formation of swarm- spores, 75. __ —, germination, 109. — infestans, abscision of spores, 72. ——,capacity of germina-~ tion, 343. — —, discharge of swarm- spores, 82*. — —, germination of gonidia, 137*. ——, germination of swarm- spores, 364*. — —, gonidia, 137*. — —, gonidiophores, 47*. — —, haustoria, 20. — —, parasitism,359,362,385. 518 Phytophthora infestans, re- sistance of spores, 346. —-—, simple sporophores, 47*. — —, swarm-spores, 108*, —:—, taking up of colouring matter, 14. — omnivora, 135. — —, parasitism, 359, 365, 385. —, parasitism, 367, 389, 392. —, simple sporophores, 47. Pietra fungaja, 42. Pilacre Petersii, 335. Pilaira, 150, 152. —, discharge of spores, 83. Pileus, 287. — in Hymenomycetes, 48. Pilobolus, 152, 155. — anomalus, 150. — —, detaching of sporangia, 83. —, conditions of germina- tion, 350. — coloured fatty matters, 7. — crystallinus, 150. — —, abjection of sporangia, 72, 83. : —, formation of spores, 74, 75+ —, membrane, 12. —, mode of life, 357. — oedipus, 163. — —, abjection of sporangia, 72*, 83. — —,resistance of spores, 346. —, structure of spores, 106. Piptocephalideae (Piptoce- phalidei), 149, 151, 153. Piptocephalis, 147, 149, 153, 155. —, formation of spores, 67. — Freseniana, 150, 153*. — —, conjugation, 149*. — —, haustoria, 20. —, parasitism, 360, 363, 385. Pistillaria hederaecola, scle- rotia, 42. — micans, sclerotia, 42. Pits, 13. — in spore-membrane, 100, Pityriasis versicolor, 376. Placodium, 223. —, calcium oxalate, 409. — cartilagineum, incrusta- tions, 409. —, distribution of Algae in thallus, 404. —-, structure .of thallus, 404. Plasmodia, 423. —, movement, 449. —, nutrition, 451. -—, phenomena of life, 449.- INDEX. Plasmodiophora, 444. — Brassicae, 448. Plastids, 7. Plectopsora, structure of thallus, 412, 413. — botryosa, structure of thallus, 414*. Pleomorphism, 126, 238. Pleospora, 186, 191, 200, 235, 239, 245, 248, 271. — Alternariae, 230, 255. — —, development of pyc- nidia, 247*. — Clavariarum, 244. —, ejection of spores, 95. —, formation of gonidia, 66. — herbarum, 220, 229, 230, 247, 255- — —, compound spores, 98. — —, development of spores, 79 ——, ejection of 95*. sey — —, germination, 114. — polytricha, 245, 247. — sarcinulae, 230. —,sclerotioid compound sporophores, 43. Pleurococcus in | Lichen- thallus, 397. Pleurostoma, 191. Pleurotus, 297. Podaxon, 317, 318. — carcinomatis, capillitium- threads, 318*. — pistillaris, 318*. Podetia (podetium), 222,402. Podosphaera, 198, 201, 233, 235, 236, 237. — Castagnei, development of spores, 79. — —, development of sporo- phores, 201*, 226*, — —, haustoria, 19*. — pannosa, 226*, Pollinaria, 305. Polyactis, 252. Polyblastia, 223. — rugulosa, Algae of thallus, 409. — —, hymenial Algae, 400, 401. — —, structure of thallus, 400. Polydesmus, 229. — exitiosus, parasitism, 362, —, spores, 68. Polyphagus, 169. — Euglenae, 162*. — —, parasitism, 361. — parasiticus, 164. —, Swarm-spores, 107, Polyplocium, 337. spores, Polyporeae (Polyporei), 288, 3335 337: —, annual layers in com- pound sporophores, 57. —, duration of growth in compound _ sporophores, 51. Polyporus, 288, 301, 303, 307. — abietinus, mycelial mem- branes, 22. — annosus, parasitism, 384. — —, structure of sporo- phore, 57. — borealis, 335. — —, parasitism, 384. —, cellulose, 13. —, clamp-connections, 2. — destructor, abjection of spores, 73. — dryadeus, parasitism, 384. — fomentarius, cellulose, 8. — —, membranes, 12. ——, periodic growth of compound _ sporophores, 57+ ——, structure of sporo- phore, 58. — fulvus, 307. — —, parasitism, 384. —-—, structure of sporo- phore, 58. —, growth of compound sporophore, 50, 57. — hirsutus, hairs, 59. — hispidus, hairs, 59. — igniarius, 303, 307. — —, cellulose, 8. — —-, parasitism, 384. —-—, periodic growth of compound sporophore, 57. — lucidus, structure of spo- rophore, 59*. —, membranes, 12. — mollis, parasitism, 384. — obvallatus, 337. — officinalis, cellulose, 8. — —, membranes, 12. — —, secretion of resin, 10. — ptychogaster, 334, 335. — Ribis, periodic growth, 57. — sulphureus, 384. — tuberaster, mycelium, 42. — umbellatus, 304. — vaporarius, _ parasitism, 384. — versicolor,membranes, 12. — volvatus, 337. — zonatus, membranes, 12. — —, periodic growth, 57. Polysaccum, 309, 326, 327. —, formation of spores, 63. parasitism, Polystigma, 191, 200, 235, 236, 239, 240, 241, 258, 259, 285. — fulvum, 199, 215. —, gelatinous membranes, 9. —, lipoxeny, 388, 389. —, parasitism, 386. —rubrum, 199, 215, 226, 240. —,conditions of germination, 350. — —, parasitism, 362. — stellare, mycelial strands, 22, 23. —, stroma, 43. —, structure of sporophore, 57+ Pore, Igr. Pores in Polyporee (Poly- porei), 288, Poronia, 244. Precursors of ascocarps in Ascomycetes, 244. Predisposition for parasites, 224, 359» Primordium of the myce- lium, 110, 178. — of sporophore, 199, 215, 218, Procarpium (procarp), 120, Promycelium, 111, 177. Prosporangium, 163. Protagon-mixtures, 300. Prothallium, 121. Protococcus in Lichen- thallus, 397*. Protomyces, 132, 171. —, capacity of germination, He —, germination, 109. —, ejection of spores, 85. —, formation of spores, 61. — macrosporus, 171. — —,cellulose-membrane, 8. — —, conditions of germina- tion, 351. — —, development of spores, : 172, ——, ejection of spores, 89, gt. ro gee parasitism, 363, 365, 386, 389. — —, resting spores, 172*. — —, structure ofspores,106,. — Menyanthidis, 166. — pachydermus, 172. —, resting state of spores, 345. Protomyxa aurantiaca, 446. Protoplasm, 6, — in Bacteria, 455. — in Mycetozoa, 422, 423, 425, 426. Protothallus, 405. INDEX, Protozoa, 475. Psalliota, 291, 297. Pseudo-lichens, 416. Pseudo-parenchyma, 3,5,405. Pseudo-peridia, 275. Pseudopodia, 423, 426. Pseudospora, 447. Psora, structure of thallus, 404. Psoroma, Algae of thallus, 409. — gypsaceum, incrustation, 408. — lentigerum, secretion of calcium, 1. — —, calcium oxalate, 408. —sphinctrinum, Algae of thallus, 404. —, structure of thallus, 404. Pterula, 29. Ptychogaster albus, 335. Puccinia, 279, 282. — Aegopodii, 285. — Alliorum, 277. — Anemones, 277. — —, parasitism, 393. — Asari, 285. — Berberidis, 279, 283, 284. — Caricis, parasitism, 387. — coronata, parasitism, 387. ——, structure of spores, 100. —, detaching of spores, 68. —, Falcariae, 279. —— —, parasitism, 387. —, formation of spores, 62*. — fusca, 277, 281. — Galiorum, 277. — graminis, development of aecidia, 275*, 276*. ——, capacity of germina- tion, 345, 348. — —, development of spores, 62*. — —, germination, 280%, — —, germ-pores, 100. — —, parasitism, 387, 389. — —, rest of spores, 345. — —, spermogonia, 276*. —-—, structure of spores, Iol. — Malvacearum, 284. — Moliniae, parasitism, 387. — Pimpinellae, parasitism, 387. — Pruni, 285. — reticulata, structure of spores, 100. — Rubigo vera, 283. — —, germination, 280*. — —, parasitism, 387, 389. —, spores, 68, 98. —, structure of spores, 100. T10*, 519 Puccinia suaveolens, 277. —-— , parasitism, 359. — Tragopogonis, parasitism, 387, 391. — Violarum, parasitism, 387. Putrefactive processes in- cited by Bacteria, 481. Pycnidia, 49, 225, 239, 246. —, large-pored, 248. —, small-pored, 248. Pycnis sclerotivora, 247. Pycnochytrium, 167. Pycnogonidia, 225, 239, 246. Pycnospores, 225, 239, 246. Pyrenocarp, 187. Pyrenomycetes, 200. ~~ as Lichen-fungi, 396. —, development of spores, 78. —, ejection of spores, 91, 97. —, hyphal weft, 4. —, number of spores, 79. —, stromata, 50. —, structure of ascus, 96. Pyrenula, 192, 223. — minuta, 246. —nitida, structure of thallus, 411. — —, thallus, 402. — olivacea, 246. Pyronema, 190, 198, 224, 231, 234, 237, 239. 186, 187, ‘— confluens, 208. — —, development of sporo- phore, 209*. Pythium, 234. — de Baryanum, 135, 137. — —, parasitism, 382. —, development, 135, 137. —, discharge of spores, 82. — endophytum, 139. — gracile, fertilisation, 133*. — intermedium, 137. — —, parasitism, 382. — megalacanthum, parasit- ism, 382. —, mode of life, 132. —, parasitism, 359, 363, 382, 389, 392. — proliferum, 135. — —, rest of spores, 345. —, rest of spores, 345. —, swarm-spores, 107, — vexans, 135, 232. Quaternaria, 218. —, discharge of spores, 97. Queletia, 318. Racodium cellare, 22. —rupestre, structure of thallus, 411. 520 Ramalina, soredia, 415. Reaction of host on parasite, 366, Receptaculum, 17, 48, 188, 312. Recurrent fever, 486, 488. Reduction in the course of development, 125, Resin in Boletus, 15. Resin-excretions, 10, Resin-flux, 384. Resistance in spores, 343. — in Bacteria, 476. Resting gonidia, 144. — mycelia, 230, 245. — sporangia, 144, — spores, 345. — — in Bacteria, 460. — states, transitory in My- cetozoa, 427. * Reticularia; 431, 440. — umbrina, 439. Rheotropism in plasmodia, 449. Rhipidium, 144. Rhipidonema, structure of thallus, 414. Rhizidieae (Rhizidiei), 162, 169, 170. Rhizidium, 164, 165. Rhizines, 402. Rhizocarpon, structure of thallus, 405. Rhizoids, 45, 59, 402. Rhizomorpha fragilis, 28. —, parasitism, 383, 384. — subcorticalis, 28, — subterranea, 28, Rhizophydium, 164. Rhizopoda, 444, 475. Rhizopogon, 308. —, formation of spores, 63. Rhizopus, 152. — nigricans, 152, 154. — —, conjugation, 148*. —, discharge of spores, 83. Rhytisma, 186, 240. —acerinum, ejection of spores, 87, 92. — Andromedae, 224. — —, germination, 111*. — —, parasitism, 358, 393. — —, structure ofspores,102. —, asci, 76, —, conditions of germina- tion, 350. —, lipoxeny, 388. —, parasitism, 389. —, stroma, 43. — —, structure, 58. —, structure of sporophore, 57 Rind of compound sporo- phore, 58. INDEX. Rind (rind-layer) of Lichen- thallus, 403. Roccella, Algae of thallus, 409. — fusiformis, incrustations, 408. — —, calcium oxalate, 409, ——, structure of thallus, 406, — Montagnei, 246, —, soredia, 415. —, structure of thallus, 404, 406. Rod-like forms in Bacteria, 458. —, gonidia, 331. Roesleria hypogaea, charge of spores, 96, Roestalia, 388. Root-hairs, 45, 54, 59- Rosellinia Aquila, structure of ascus, 96. — quercina, 215. — —, mycelium, 42. Rotting in orchard fruit, dis- 379. Rozella, 169, 444. —, parasitism, 368, 395. — septigena, parasitism, 395. Russula, 297, 304. — adusta, 298. —, calcium oxalate, 11, — foetens, var. lactiflua, 300. — integra, 298. ——, structure of sporo- phore, 58. — olivacea, 298. , pseudo-parenchyma, 3. Rutstroemia (see Sclero- a 41. , ejection of spores, 86. Ryparobius, 208. Saccharomyces, 267, 270, — albicans, 267. — —, parasitism, 377. — apiculatus, 271, 272. — —, mode of life, 357. —, cell-nucleus, 6 — Cerevisiae, 267. — —,resistance to effects of heat, 347. — —, sprouting, 4*, 267*. — —,swelling of membrane, 10, —, conditions of vegetation, 353+ — ellipsoideus, 267, — —, formation of spores, 268%, —, germination, 114, — ’ glutinis, 292; — mesentericus, 358. 132, 263, Saccharomyces, Mycoder- ma, 267, 268, 269, 358, rt; ae — Pastorianus, 267, —, pleomorphism, 270, —, secretion of ferments, alleged, 355+ —, thallus, 5. Saccobolus, spores, 92. —, structure of spores, 102. Sagedia aenea, 246, — callopisma, 246. — carpinea, 246. — netrospora, 246, — Thuretii, 246. — Zizyphi, 246. Salts of iron in Lichen-thal- lus, 408. Sap-cavities (vacuoles), 6 Saprolegnia, 143. —, discharge of spores, 82. —, formation of spores, 74, — hypogyna, 141, 142, — monoica, 141, —, parasitism, 359, 393. —, simple sporophores, 46, —, sporangia, 46. —, swarm-spores, 107, 108. Saprolegnieae (Saprolegniei), 141, 232. —, capacity of germination, ejection of 343. —, cell-nucleus, 6, —, cellulose-membrane, 8. —, discharge of spores, 82. —, parasitism, 375, 395- —, resistance of spores, 345. —, rest of spores, 344. —, simple sporophores, 46. Saprophytes, 356, 357, 480. —, facultative, 356. —, obligate, 356. Sarcina, 473. — ventriculi, 459. Sarcinula, 229. Sarcogyna, numberof spores, 79+ Scales on compound sporo- phores, 59. Schizomycetes, 454. Schizonella, 176. Schizophyllum, 302. Schizophytes, 474, 476. Schizosiphon in Lichen- thallus, 398. Sclerangium, 315. Scleroderma, 309, 311, 313, 315. —, formation of spores, 63. —, mycelial strands, 23. Sclerosis of membranes, 9. Sclerotia, 18, 30. Sclerotia, development, 34. —, further development, 37. --, gelatinous membranes, 10. —, hyphal weft, 3. — in Mycetozoa, 427, 428. —, membranes, 12. —, pseudo-parenchyma, 3. —, resting state, 37. Sclerotinia, 41, 200, 260. (See also Peziza.) — ciborioides, organs of at- tachment, 21. — —, parasitism, 380. — —, resistance of spores, 346. —, development of spores, 78. — Fuckeliana, 219,224, 238, 251. — —, compound phores, 38%, ——, conditions of ger- mination, 350, 351. — —, germination, 113. — —, gonidiophores, 48. — —, organs of attachment, ai. — —, parasitism, 380. — —, sclerotia, 31*, 34, 37, 38*, 39. —, gelatinous membranes, 9. —, lipoxeny, 388. —, membranes, 12. —, organs of attachment re- sembling haustoria, 21. —, parasitism, 359, 360, 380, 389, 392. —, sclerotia, 30, 34, 39- — Sclerotiorum, 200, 218, 224. — —, compound sporo- phores, development, 53*, ar9*. ——, conditions of ger- mination, 351. — —, ejection of spores, 87*. — —, germination of sclero- tia, 38, 39. — —, organs of attachment, 21. — —, parasitism, 359, 380. — —, sclerotia, 30, 31*, 34, 37, 39- — tuberosa, 243, 260. — —,organs of attachment, 21. Sclerotium, 40. — areolatum, 41. — Clavus, 41. — Cocos, 42. — compactum, 41. — complanatum, 42. — cornutum, 42. sporo- INDEX. Sclerotium crustuliforme,42. — Cyparissiae, 41. — durum, 251. — echinatum, 41, 238, — fulvum, 41. — lacunosum, 42, — laetum, 42. — muscorum, 32. — mycetospora, 42. — pubescens, 42. — Pustula, 41. — roseum, 41. — scutellatum, 42. — Semen, 41. — stercorarium, 32, 42. — stipitatum, 42. — sulcatum, 41. — truncorum, 42. — vaporarium, 42. — varium, 41. — vulgatum, 42. Scytonemain Lichen-thallus, 397%, 398. Sebacina incrustans, 306. Secotieae (Secotiei),3 10,313. Secotium, 310, 313, 337. — erythrocephalum, 337. — —,compound sporophore, 310*, Semen, 130. — multiplex, 98. Sepedonium, 245, 252. Septicaemia, 486. Septoria, 252. Sexual organs, 49, 233. —, assumed in Basidiomy- cetes, 332. Sexuality, 120. — in Ascomycetes, 237. Short rods (Bacteria), 458. Silk-worms, diseases in, 486, 489. Simblum, 326. Simple sporophores, 46. — —, germination, 114*. — —, structure of thallus, 404, Sirosiphon in Lichen-thal- lus, 398. Solorina crocea, Algae of thallus, 409. — saccata, Algae of thallus, 409. — —, incrustation, 408. Sordaria, 191, 198, 199, 210, 235, 243, 260. — Brefeldii, attachment of spores to ascus, 88. —, conditions of germina- tion, 350. — coprophila, 243. — —, structure of spores, 103. — curvula, 243, 261, 521 Sordaria curvula, capacity of germination, 344. — decipiens, 243. —, ejection of spores, 86, 88, g1*, — fimicola, 210, 261. — fimiseda, 192. — —, capacity of germina- tion, 343. — —, development of spores, 78. — —, ejection of spores, 85, 92. — —, germ-pores, ror. — —, number of spores, 79. — —, structure of spores, 103, 104*. —, germination, 111. — minuta, 243, 261. ee. ejection of spores, g1*, —, mode of life, 357. —, number of spores, 79. — pleiospora, number of spores, 79. —, structure of spores, 103, 106. Soredia, 244, 401, 415, Soredia-heaps, 416. Sorosporium, 175, 176. — Saponariae, 172, 179. — —, parasitism, 391. — —, rest of spores, 345. Sorus, 167, 416. Spathulea, 189. Spermatia, 199, 211*, 239, 240, 257, 276*. —, supposed in Basidiomy- cetes, 333. —, doubtful, 242. Spermogonia, 199, 211*, 239, 240, 241, 257, 276%, gor, Sphacelia, 227, 252. Sphacelotheca, 173. — Hydropiperis, compound sporophores, 174*. Sphaerella Plantaginis, 220. Sphaeria discretia, fatty matters, 7. — eutypa, fatty matters, 7. —inquinans, ejection of spores, 95. — Lemaneae, 214. — —, ejection of spores, 85, 94. — obducens, of spores, 79. — —, ejection of spores, 95. — oblitescens, 245. — praecox, germination,115. —-—, structure of spores, 104. — Scirpi, development of spores, 79. development 522 Sphaeria Scirpi, ejection of spores, 85, 93*. ae structure of spores, 99*, 102, 103. — Stigma, fatty matters, 7. Sphaeriaceae (Sphaeriacei), ejection of spores, 85. —, formation of gonidia, 66. —, structure of spores, 102. Sphaeriae compositae, 186. Sphaerobolus, 326, 329, 330, 331, 332, 340. —, coloured fatty matters, ¥ —, mycelial strands, 22. —, stellatus, 328. Sphaeromphale, 192. Sphaerophoron, 193. — coralloides, development of spores, 78. — —, discharge of spores, 96%. — —, gonidia, 398*. — —, incrustations, 408. —, discharge of spores, 96*, 97. —, structure of thallus, 404, . 406, Sphaeropsideae (Sphaerop- sidei), 251, 252. Sphaeropsis, 252. Spheconisca, 416. Sphere-yeast, 156. Sphyridium, 200, — fungiforme, 221. — placophyllum, 221. Spicaria, 245. Spilonema, 242. —, structure of thallus, As a Spilosphaeria, 252. Spinellus, 152. Spiral forms in Bacteria,458. Spirillum, 456, 458, 459, 473- — amyliferum, 455, 461. Spirochaete, 458, 459. — Obermeyeri, 488. Spora, 128. Sporae cellulosae, 98. — compositae, 98. — multiloculares, 98. Sporangia (sporangium), 45, 73, 130, 319. — in Mycetozoa, 429, 434. — Sporangiola, 152. Spore, 130. Spore-development (see also - Spore-formation), 60. —, acrogenous, 61. — by free cell-formation, 61. — —, cell-division, 61. — intercalary, 61. Spore-formation, branched concatenate, 66. INDEX. Spore-formation, by cross- septation, 67. —, endogenous, 73. — in Bacteria, 460, 465. — in Mycetozoa, 429. —, simple concatenate, 66. —, simultaneous, 63. —, successive, 63. —, sympodial, 65. Spore-germination, 109. Spore-groups, 99. Spore-heads, 63. Spore-initial cells, 98. Spore-membrane, chemical properties, 104. Spore-membranes, 83. Spore-mother-cells, 48, 60, 98. Spore-primordia, 98, Spore-receptacles, 48. Spores, 45, 59, 121, 128. —, abjection, 68, 72. —, abjunction, 61. —, abscision, 68. —, appendages of, 102. —, capacity of germination, 343+ —, compound, 98. —, conditions of germina- tion, 349. —, delimitation, 61, 68. —, detaching, 68. —, discharge, 82. —, fatty matters, 7. —, germination, 109. — of Bacteria, 461. — of Mycetozoa, 421, 440, 124, 441. —, pluricellular, 98. —, resistance, 346. —, resting state, 345. —, ripeness, 68, —, septate, 68, 98. —, structure, 99. Sporidesmieae (Sporidesmii), Sporidesmium, 68, 229. —, spores, 68. Sporidesms, 99. Sporidia, 111, 130, 177. —, capacity of germination, 343- —, whorl of cylindrical or subulate (Kranzkérper), 177. Sporoblasts, 99. Sporocadus, 252. Sporocarpium (sporocarp), 121, 185, 239. Sporodinia, 147, 148, 149, 150, 151, 152. — grandis, 147, 150, 154. —, resistance of spores, 346. Sporodinia, resting time of © spores, 345. Sporogenous layer (hyme- nium), 49. Sporophore, 45. — in Mycetozoa, 429. Sporophyte, rar. Sporormia fimetaria, spores, 99- Sporula, 130. Spread of parasite in host, 389. Sprout-gemmae, 155. Sprout-germination, 110. Sprouting Fungi, 4*, 5, 60. —, form, 4*, 5, 267. —, germination, 114. — —, in Ustilagineae, 177. —, growth, 155. —, mucilage, 9. Spumaria, 436, 440. Spumella vulgaris, 475. Steganosporium, 252. Stemoniteae (Stemonitei), 427, 434, 439, 441. Stemonitis, 423, 431, 432, 433, 438, 440. — ferruginea, formation of sporangia, 432*. — fusca, 427. Stephensia, 196. Stereocaulon, thallus, 410. —, podetia, 402. — ramulosum, thallus, 397*. Stereum (see also Thele- phora), 303, 304. — hirsutum, development of sporophore, 53*. — —, fatty matters, 7. — —, parasitism, 384. — —, periodic growth, 57. ——, structure of sporo- phore, 57, 58. — rubiginosum, 303. — tabacinum, 303. Sterigma, 61. Sterigmata in spermatia, 240. Sterigmatocystis, 206, 256. —, parasitism, 369. Stichococcus in Lichen- thallus, 397. Sticta, Algae of thallus, 409. — aurata, incrustation, 408. — fuliginosa, structure of thallus, 403*. — glomulifera, Algae of thallus, 409. —, incrustation of thallus, 408, — pulmonacea, thallus, 187*. ——, structure of thallus, 406, Algae of Algae of Sticta, structure of thallus, 406, Stictina, Algae of thallus,409. Stictosphaeria, 191,218, 241. —, discharge of spores, 97. — Hoffmanni, 258. Stigmatea, 244. Stigmatomma _ cataleptum, origination of thallus, 400. — —, hymenial Algae, 400, 401. Stigmatomyces Baeri, 263. — —, development, 263%. — Muscae, development, 263*, Stigonema in Lichen-thallus, 398. Stilbospora, 252. —, spores, 68, Stilbum, 29, 252, 334. Stipes in sporophore of Hymenomycetes, 287. Stratum corticale, 403. — gonimon, 417. — medullare, 403. Striation of spore -mem- brane, 100. Stromata, 48, 186. Stylospores, 154, 225, 239, 246, 279. Stysanus, 252. Suberisation of membranes, 9. Subhymenial layer or tissue, 301. Sulphur in Bacteria, 455, 471. Supply of food, a condition of germination, 351. Suspensor in zygospores, 148. Swarm-cells, 107. — in Mycetozoa, 422. Swarm-spores, 60, 107, 129. —, capacity of germination, 343. —, discharge, 82. —, resistance, 346. Symbiosis, 356. Synalissa, structure of thal- lus, 413, 414*. — symphorea, thallus, 397*. Syncephalis, 146, 153, 154. — curvata, I50. —, formation of spores, 67, r17. — furcata, 153. —, haustoria, 20. — nodosa, 149, 150. — parasitica, 360, 363, 385. —, secondary mycelium, 45. Synchytrium, 162, 167, 168, 169, 444. Algae of INDEX. Synchytrium, rest of spores, 345+ — aureum, 160. — —, rest of spores, 345. —, capacity of germination, 349. — Oenotherae, 168. —, rest of spores, 345. — Stellariae, 168, 169. — —, propagation, 168*. — Succisae, 169. — Taraxaci, 168. — —, rest of spores, 345. Synechoblastus, 198. —, structure of thallus, 412. Systematic arrangement of Fungi, 132. Syzygites, 151. — ampelinus, 151. Taphrina, 265. —, germination, 115. Tarichium, 159. Teeth, caries, 472. Tela contexta, 5. Teleutogonidia, 281. Teleutospores, 279, 282, 339. —, resting state, 345. Terfezia, 195. Terminology of Fungi, 128, 130. Tetrachytrium triceps, 170. Thalloidima candidum, cal- cium oxalate, 409. ——, structure of thallus, 404. Thallus, 1. —, branching, 1. —, crustaceus, 402. —, differentiation, 17. —, fertile (stroma), 186. —, filamentosus, 4o1. —, foliaceus, 401. —, frondosus, 401. —, fruticulosus, 401. —, lepodes, 402. —, placodes, 4o1. —, thamnodes, 401. Thamnidium, 152. —., discharge of spores,82,8 3. — elegans, 150. Thamnolia,incrustation,408. —, structure of thallus, 406. — vermicularis, calcium ox- alate, 409. Thamnomyces, 186. —, branching, 5r. Thecae (asci), 76. Thecaphora, 176. — hyalina, 177. — Lathyri, 177, 179. Thecaspores, 129. Thelephora crocea, mycelial membranes, 22. 523 Thelephora hirsuta, mem- branes, 12. — —, mycelial membranes, 22. —, membranes, 12. — mesenterica, gelatinous membranes, 13. —, mycelial membranes, 22. — Perdix, 307. — —, parasitism, 384. — setigera, mycelial mem- branes, 22. — suaveolens,mycelial mem- branes, 22. Thelephoreae(Thelephorei), 288, 333, 338. —, mycelial membranes, 22. Thelidium minutulum, 224. — —, Algae of thallus, 409. — —, germination, 399*. — —, origin of thallus, 400. — —, perithecia, 190*. — —, structure of thallus, 410%, Thermotropism of plasmo- dia, 450. Thrush (aphthae), 377. Thyrea pulvinata, structure of thallus, 414*. —, structure of thallus, 413. > Tilletia, 172, 174, 177, 178, 180, 181. — Caries, 179. — —, capacity of germina- tion, 344. — —, germination, 177*. — —, parasitism, 385. — —, resistance of spores, 346. —, parasitism, 367. Tinder-fungus, 3. Tinea (herpes), 376. Tissue, hymenial, of Léveillé, 302. —, intralamellar 301. —, subhymenial, 301. Tolyposporium Junci, 177. Torula, 252. Trama, 301, 309. Trametes Pini, 304, 307. — —, duration ofgrowth, 51. — —, membranes, 12. — —, mycelial membranes, = — —, parasitism, 304. — —, periodical growth, 57. — radiciperda, secretion of ferment, 355. — —, parasitism, 384. Transmutation of host, 395. Tremella, 305. — Cerasi, 306, 331. (trama), 301, 303, 524 Tremella, foliacea, 306. —, formation of spores, 62. —, gelatinousmembranes, 13. — mesenterica, 331. — violacea, 306. Tremellineae (Tremellini), 271, 287, 288, 298, 301, 303, 305, 329, 333, 338. —, conditions of germina- tion, 350. —, fatty matters, 7. —, gelatinous membranes, 9. —, gemmae, 60, 61. Tremellodon, 288, 305. — gelatinosus, hair-forma- tions, 59. Trentepohlia in Lichen-thal- lus, 397, 398*. Trichia, 431, 433, 435, 437; 4395 440. — chrysosperma, 438, 440. ——, capillitium, spores, 437*. — clavata, 434. — fallax, 431, 437, 438, 439, 441. — —, capillitium, 437%. — furcata, 441. — pyriformis, 441. — rubiformis, 448. — Serpula, 434. — varia, 434, 438, 441, 448. —-—, germination, swarm- cells, 422*. Trichiaceae 427, 441. Trichiae, 436. Trichogyne, 198, 209, 213, 215, 234, 237. Trichophyton parasitism, 376. _ Trichothecium roseum, pa- rasitism, 380. ——, resistance of spores, 346. —, spores, 68. Triphragmium, 281, 282. — echinatum,parasitism, 358. — —, structure ofspores, 100. —, spores, 98. — Ulmariae, parasitism, 358. Trophoplasts, 7. Trophotropism in plasmodia, 449- Truffles, 195. —, glycogen, 6. Tube-germination, r1o. Tuber, 195. — aestivum, 195. — —, development of spores, 80. ——, structure of spores, 100. spores, (Trichiacei), tonsurans, INDEX. Tuber, asci, 76. — brumale, development of spores, 80*, —, conditions of germina- tion, 352. — dryophilum, 195. — excavatum, 195. — melanosporum, 195. — —, development of spores, 80. — —,structure ofspores, 100. — mesentericum, 195, 196. —, number of spores, 79. — rapaeodorum, 195, 196. — rufum, compound sporo- phore, 196*. Tuberaceae (Tuberacei),193, 195. —, clamp-connections, 19. —, discharge of spores, 97. —, hyphal weft, 3. Tubercularia, 252. — vulgaris, 244. Tubuli in sporophore of Polyporeae, 288. Tubulina (Tubulinae), 448. —, experiments in germina- tion, 421. Tubulus of perithecia of Pyrenomycetes, 191. Tuburcinia, 175, 176, 177. — Trientalis, 178, 180, 181. —-—, capacity of germina- tion, 345, 349. — —, parasitism, 365, 391. — —, rest of spores, 345. Tulostoma, 287, 326, —, capillitium, 12. — mammosum, basidia,310*, —-—, compound _ sporo- phore, 327*. — pedunculosum, sclerotia, 42. Tympanis, 245. — conspersa, spermogonia, 240°, — —, number of spores, 79. — saligna, number of spores, 79- Typhula, 329. — caespitosa, sclerotium, 41. —, clamp-connections, 2. — erythropus, 41. — Euphorbiae, 33, 41. — graminum, 33, 41. —, growth of compound spo- rophore, 52. —gyrans, inception of sporophore, 49. — —, gelatinous membranes, — —, membranes, 12. ——, sclerotium, 30, 33*, 34) 35, 37) 395 42. Typhula gyrans, lactea, scle- rotium, 41. : — phacorrhiza, sclerotium, 33"; 37) 42 — Todei, sclerotium, 41. — variabilis, development of sporophore, 52. — —, sclerotium, 30, 33, 34, 37, 38, 42. Ulothrix in Lichen-thallus, 397: Umbilicaria pustulata,growth in thickness of thallus, 407. —, number of spores, 79. Uncinula spiralis, 225. Urceolaria cinerea, structure of thallus, 405. — scruposa, calcium oxalate, 409. Uredineae (Uredinei), 120, 132, 274, 287. —, aecidia-forming, 274. —, capacity of germination, 343» 349. —, coloured fatty matters, 7. —, conditions of germina- tion, 350. —, germination, 113. —, germ-pores, 1o1. —, gonidiophores, 50. —, haustoria, 20. —, parasitism, 359, 361, 363, 366, 367, 386, 387, 389, 390, 393- —, spores, abscision, 71*. — —, resistance, 346. — —, rest, 344. — —, structure, 100, 106. —, structure of sporophore, 57- —, tremelloid, 274, 283, 339. Uredo, 279. — Symphyti, 282, Uredo-layer, 279. Uredogonidia, 281, Uredospores, 279. —, capacity of germination, 343- —, formation, 62. —, germination, 111. —, structure, 1o1*, Urocystis, 172, 175, 177. — occulta, 180. ——, capacity of germina- tion, 344. — —, parasitism, 391. —, structure of spores, 104. — Violae, 178, 181. Uromyces, 281, 282. — appendiculatus, germina- tion, 361*, ——, germination of spo- ridia, 364%. Uromyces appendiculatus, parasitism, 387. — Belienis, 279. — Cestri, 279. — Dactylidis,parasitism, 387. — Phaseolorum, 281.° — — parasitism, 387, 389. — Pisi, parasitism, 368, 388, 391. — Scrophulariae, 279. — scutellatus,parasitism, 368. —, spores, 98. — —, detaching, 68. — —, formation, 62. — tuberculatus, parasitism, 358. — Viciae Fabae, 277. Usnea barbata, Algae of thallus, 398*. — —, chemical properties, 407. — —, incrustation, 408. — —, soredia, 415. ——, structure of thallus, 402*, — —, thallus, 187*. —, structure of thallus, 404, 405, 406, Ustilagineae (Ustilaginei), 120, 132, 172, 176, 179. —, capacity of germination, 344. —, conditions of germina- tion, 350. —, haustoria, 19. —, parasitism, 359, 362, 364, 367, 385, 390, 391, 393. —, spores, rest, 345. — —, structure, roo, Ustilago, 174. — antherarum, 179. — Carbo, 177, 179, 180, 181. ——, capacity of germina- tion, 344. — —, conditions of germina- tion, 349. — —, germination, 178*, — —, parasitism, 367. —-—, resistance of spores, 346. — Cardui, 177. — Crameri, capacity of ger- mination, 344. — destruens, 177, 179, 180. —-—, capacity of germina- tion, 344. — —, conditions of germina- tion, 349. — —, resistance ‘of spores, 346. — flosculorum, 177, — hypodytes, 172, 175. INDEX. Ustilago flosculorum, parasi- tism, 391. — Ischaemi, 175. — —, formation ofspores,68. — Kolaczeckii, capacity of germination, 344. — Kiihniana, 177, 179. — longissima, 173, 179, 183. — —, germination, 178*, — Maidis, 179, 181. — olivacea, 173. — Rabenhorstiana, capacity of germination, 344. —receptaculorum, _ struc- ture of spores, 102. — Tragopogonis, 172, 182. — —, development of spores, 175*, — —, germination, 178*, — —, parasitism, 391. — Tulasnei, capacity of ger- mination, 344. — utriculosa, 177. — Vaillantii, 177, 179. Ustulina, 186, 218, 244, 248, 260. Uterus, 308, Vacuoles (sap-cavities), 6, 424. Valsa ambiens, 258. — —, number of spores, 79. — nivea, spermogonia, 240*, — —, number of spores, 79. — salicina, number of spores, 79 —, structure of spores, 102. Valseae (Valsei), 191, 192. —, discharge of spores, 97. Vampyrella, 447, 453> — pendula, 447. — Spirogyrae, 447. — vorax, 447. Variolaria, 416. ; Vegetation, general condi- tions, 352. Veines aériféres, 195. — aquiféres, 195. Velum, 289, 291. — partiale, 290. — universale (volva), 290. Venae externae, 195. — internae, 195. — lymphaticae, 195. Vermicularia, 252. — minor, fatty matters, 7, — —, sclerotium, 41, Verpa, 189, Verrucaria, 192, 222. —, Algae of thallus, 409. — Carpinea, 246, — Gibelliana, 246. THE END. 525 Verrucarieae (Verrucariei), 242. Verticillium, 245, 249, 252. Vibrio, 458, 459, 473. Vibriones, 458. Volva, 290. Volvaria, 292, 295, 297. Warts on compound sporo- phores, 59. Water-content, 6. — -supply, as a condition of germination, 375. Whorl of sporidia (Kranz- k6rper), 177. Wine-yeast, 269. Witches’ brooms, 266, 368, 390. Withdrawal of water, influ- ence on germination, 346. Woronina, 161, 169, 444. —, parasitism, 395. Woronin’s hypha, 199, 218. Xylaria, 186, 192, 199, 236, 244, 260. —, branching, 51. — bulbosa, sclerotium, 41. —, compound sporophores, development, 56. — —, growth, 50, 51. — pedunculata, structure of spores, 102. — —, chemical behaviour of spore-membrane, 105. — polymorpha, development of sporophore, 216*. — —, development of spores, 8 78. Xylarieae(Xylariei), 186,236, 248, 260. —, discharge of spores, 97. Xyloma, 43, 190. Xylostroma, 22. Yeast-fungi, 4*, 5, 267, 270, 358. Yeast-fungus of alcoholic fermentation, 267. Yeast-mucilage, ro. Zeora, 223. Zoogloea, 457, 459. Zoospores, 107. Zygochytrium, 146, 151, 169. — aurantiacum, 156. Zygomycetes, 132, 145. —, rest of spores, 345. —, thallus, 1. Zygospores, 129, 145. —, formation, 147. —, resting state, 344, 345. XS) A i Ra mate meaatee lea tatle) ai Ree ry wh ete aie te nN Wignttotanentsteterntetmtat etsy POR RS SSS ue aa a si NN Y He oe . a a BARR a ne Na J / SSN oy s) .f *. 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