Inv- in the '
MYCOLOGY.
DR. OSCAR BREFELD.
Part XIII.
Smut Fun^i (1 I.-iinha-ulia IV).
(Continuation of Parts \ . XI and Xll).
Conteii1
O. BREFELD, R. I >n by Smuts and
Natural Distribution of Smut Diseases.
With Two Phototype Plates.
MIELD BY HF.r
Investigations in the General Field of
MYCOLOGY.
Continuation of the Moulds and Yeasts,
BY
DR. OSCAR BREFELD.
Part XIII.
Smut Fungi (Hemibasidia IV).
(Continuation of Parts V, XI and XII).
Contents :
O. BREFELD, R. FALCK, Blossom Infection by Smuts and
Natural Distribution of Smut Diseases.
With Two Phototype Plates.
'"•".** *
-
MUNSTER i. W.
PUBLISHED BY HEINRICH SCHONINGH.
COPYRIGHT 1912
BY
FRANCES DORRANCE.
150 Copies.
Privately Printed and Distributed.
CONTENTS.
Preface.
Introduction.
Blossom infection by smut fungi.
Methods of blossom infection.
Blossom infection in wheat.
Blossom infection in barley.
Infection in oats.
Blossom infection in Melandryum.
Infection of water plants.
The Infection of the Maize plant.
The Infection of Indian millet.
The Infection of Panicum (Rispenhirse) and Italian millet.
Final consideration.
On nitrogen assimilation.
PREFACE.
The present investigations, which have chiefly as subject matter the newly discovered
blossom infections by smut fungi and, in connection with them, the natural distribution of smut
diseases, form the continuation of the work on smut fungi already published in 3 parts, Vols.
V, XI and XII, of this work.
It would not have been possible to carry out these new investigations to the extent here
reached, if the Cultusministerium, at my suggestion, had not been so very kind as to grant the
requisite means.
It is a great satisfaction to me to be able to express at this place my respectful thanks.
Professor BREFELD.
Breslau, September, 1905.
INTRODUCTION.
The investigations on smut fungi diseases, published in Parts V, XI and XI I ' of this work,
date back, in their beginning, to the second half of the 70*5 in the last century. It was a time
wiu-ii a noticeable standstill had come in the investigations of smuts and smut diseases. More
than 25 years had already elapsed since Tulasnc2 had carried through methodically the germina-
tion of smut spores in water and had ascertained that these spores did not germuiatt» into
mycdia, but into short germinating tubes which, becoming fructificative with an eany cessa-
tion of their growth, form conidia. Tulastte designated this fructificative kind of spore germi-
nation as germination with promycelia and sporidia. He had observed also an almost corre-
sponding fructificative germination in the talen tospores of Uredo and had used here too the
same designation by which he had already expressed hypothetically the close connection of both
form of fungi.
Meanwhile experimental infection had been carried out with smut spores whose peculiar
germination had now been ascertained by Tulasne, in order to develop smut diseases in the differ-
ent proper host plants. These experiments were made chiefly by /. Kuhn3 and showed that the
mature plants are resistent to and insured against the attacks of smut germination and that infec-
tion remains limited to the short stage of the germination of the seed. Disinfection with solutions
of copper sulfate, previously carried out with success, — thus killing the smut spores, — obtained
here its natural explanation and valuation4. The germinating seedlings are attacked in the earth
by the germs of infection which come in contact with them. They penetrate quickly through the
young tissues into the meristematic tissue of the seedling and continue their growth here, in order
to form later the smutted places on the completely matured plants, usually in their ovaries.
The place on which the smut appears on the plants attacked lies accordingly as far distant
as possible from the place of infection in the young seed. During the period of development of
the host plants, nothing may be seen of the effect of the infection. The accommodation of the
parasites to their hosts is thus absolutely complete. The parasite appears externally only in the
last stage of development.
(1) Botanlgche Untersuchungen Uber Hefenpilze. Untersuchungen aua dem Oesammtgeblete d«r
Mycologie. V. Heft. Die Brandptlze I. Verlag von ARTHUR FELIX, Leipzig. 188S. Band XI. Die Brand-
pllze II. Die Brandkrankhelten des Qetreldea. Commlsslonsverlag von HKINKK'H S« 'Hi >\1N< III. MUnster.
1895.— XII. Heft. Hemibasldll, Brandpllze III. Com missions- verlats. MUnster I. W. 1895.
(2) TULASNE, Memolre sur lea Ustllaglnees comparee* aux Ured. Ann. d. Be. nat. 3 Serle Tome 7.
1847— Seconde Memolre 8. I. Uredineea et les fstllag. Ann. d. ec. nat 4 Serle. Tome 2. 1854. As \* w.-ll
known. PREVUST before TULASNE had observed the germination of smut spores In water and frurn
this had traced smut diseases to fungi living parasltlcally.
(3) KI:HN. I)i.- Krankhi-lten der Kulturgewachse. Berlin, 1868. and later works.
(4) The fungicide action of copper on smut spores has also been stated by PREVO8T.
The knowledge already won on the one hand by Tulasne, concerning the f ructificative
germination of the smut spores, and Kuhn's discoveries on the other hand, concerning the manner
of infection of the host plants by the smut germs, were supplemented so simply and naturally that
it became easy for the imagination to form a complete picture of the etiology of smut diseases.
Smut spores, germinating fructificatively in the earth, press, with the help of the conidia formed,
into the germinating seedlings and produce the smut diseases which appear first with the com-
pleted development of the host plants.
From the discoveries already existing, scarcely a gap remained for further and new points
of attack in order to continue the investigations of smut diseases, and thus it becomes clear, that
the advancing understanding of the matter could reach a standstill as has been emphasized
already.
My investigations begin here ; — I began my observations by investigating the germination
of tj^'e sjjores of various smut fungi as far as they were accessible. In those investigations, I
had always to convince myself of the striking fact that the germination of smut spores is scanty
and inactive in water. As a rule, only a part of the spores germinate and the products of this
germination, the conidia of the promycelia, were so passive in their further germination that ger-
mination tubes were only rarely formed from them. Besides this, spores of other forms of
smut fungi behaved very negatively. They could not be brought to any germination in water ;
for example, the spores of the prevalent maize smut, which until then no one had seen germi-
nate. In the face of these phenomena of germination, the question was asked involuntarily,
how it was possible for these delicate germinating smut spores to reach the host plants and to
penetrate into them. This question became still more difficult when extended to the spores which
would not germinate at all, such as maize smut spores.
These ever returning phenomena in the germination of spores in water pointed with urgent
necessity to the fact that a gap in our knowledge must exist at this place and that without the
co-operation of further, as yet unknown, factors for the germination and development of smut
spores, the existence of smut fungi and smut diseases could scarcely be thought possible in such
general distribution as we see them in nature.
The developmental stages then suspected but still unknown, were found yery quickly when
I investigated the germination of the spores in nutrient solutions and substrata, instead of in
water. I had already carried this through successfully for a number of other fungi living para-
sitically1. It became evident first of all that the spores, otherwise germinating singly, were
stimulated at once to germination as a whole and that the smut spores which did not germinate
at all in water, such as the spores of maize smut, proceeded at once to germination, without an
exception. The development in nutrient solutions was as luxuriant as could be observed only
in other fungi living saprophytically. Who would have thought, in glancing at the abundant sapro-
phytic development, that developmental members of the most specific of all parasites were involved
here, which as yet had been observed only in definite species on living plants, and indeed only in
definite parts of those.
(1) Compare the works published In Part IV of this work.
The saprophytic nutrition referred to here took place, not only on one nutrient substratum,
but on any which were used for the culture. The parasites accordingly behaved outside of the
host plant just as do other fungi which live saprophytically and do not exist simultaneously as
parasites.
In cultures in clear nutrient substrata, it was shown further that the conidia formed by
the germination of the spores were increased in many places by direct budding without change
of form. They illustrate in this manner of reproduction different forms of budding fungi
which are characterized by the form of the bud, by the definite place of budding and the early
separation of the budded members from one another. These bud conidia, which were increased
through unceasing budding until the nutrient substrata were exhausted, are therefore proved here
to be released developmental members of our smut fungi, however much they outwardly give
the impression of ordinary yeast fungi. Some of these bud conidia are able to continue their
budding in the air also and to form conidia there which are disseminated through the air; as,
for example, the bud conidia of the maize smut. The germinating spores of the different forms
of smut fungi in nutrient solutions are illustrated in Part V of this work1 and especially the bud
0'iiidia, which, belonging there, were then pictured as they are produced at the period of exhaus-
tion of the nutrient substrata.
In Part XII of this work may be found further statements on the germination of smut
spores, especially on the morphologic decision as to spore germination in promycelia with sporidia.
In order to interpret this correctly, extensive investigations on Basidiomycetes, continued for
many years, had to take place first; — the results of which are united in Parts VII and VIII of
this work2. It was shown that the basidia of the Basidiomycetes occur in two different forms;
once as definitely organized basidia, each forming one spore from each cell, and then as unicel-
lular, unorganized basidia which produce at the tip a definite number of spores, mostly four'.
These two forms of basidia, named Protobasidia and Autobasidia, showed a striking correspond-
ence with the two forms of promycelia which were formed in the germination of the smut
spores. The formal production of the promycelia in the one type of Ustilagineae corresponds
perfectly with the form of the basidium of Protobasidiomycetes and, in the same way, the undi-
vided promycelium in Tilletia with its apically formed sporidia is formed exactly like the basidia
of .\utobasidiomycetes. The difference between the above named formal types of the smut fungi
for the one part, and the two basidia forms of the Basidiomycetes for the other part, consists
only in the fact that the number of spores in the former is still indefinite, but in the latter has
become definite4. The promycelia are therefore nothing but basidia which have not yet reached
the higher and typical formation of the basidia. The basidia of the Ustilagineae are accordingly
the first stages of the actual basidia in Basidiomycetes. They explain the natural course of mor-
phological differentiation which has held in the formation of the basidia. The organization and
(1) Compare the Illustrations on the IS plates in Part V of this work 1. c.
(1) Compare with these the Illustrations on the plates In Parts VII and VIII of this work.
(3) Compare with these the Illustrations on the plates In Parts VII and VIM (if this work.
(4) The illustrations on the plates In Parts V and XII should be compared with those In Parts
VII and VIII as mentioned above.
8
formal production in basidia are the same ; the difference consists only in the number of spores.
Therefore the Hemibasidia of the Ustilagineae have already the characteristic form of the basidia
but as yet no definite number of spores. The growth from the first stages up to the complete
basidium occurs first in the actual Basidiomycetes. The Ustilagineae are accordingly Hemibasid-
iomycetes. They pass over naturally in their types, once with divided hemibasidia, again with
undivided ones, in one direction to the Protobasidiomycetes, in the other to the Autoba-
sidiomycetes1.
In the formal sphere of the Ustilagineae with Protohemibasidia, there is the interesting
addition in the formation of Hemibasidia that there exist forms, such as those, for example,
in Ustilago longissima and also in Ustilago grandis", in which the Hemibasidium has not yet
become typical in its formation and in which the conidia always grow out again to irregular
Hemibasidia. In Ustilago bromivora3, the hemibasidia have become typical, but the conidia
still grow out to hemibasidia. Only in the later forms of the genus, Ustilago ; for instance, Ust.
carbo, Ust. maydis, Ust. sorghi (cruenta4), etc., the hemibasidium is limited in the germination
of smut spores to the single typical formation with conidia as subsidiary fruit forms, as in typical
basidiomycetes. In this limitation the gradtion is shown, through which a hemibasidium attains to
its highest formation. Compare the detailed illustrations in Part XII, where the new nomencla-
ture is based on a phylogenetic foundation.
In the entire province of morphology, cases of natural relationship passing from the simple
to the more complex cannot be ascertained in as clear and convincing a way as they exist here in
the forms of hemibasidiomycetes and actual basidiomycetes. This elucidation of the peculiar
formation of the basidia has become one of the now immovable supports of the natural classi-
fication of fungi, as based on the comparative morphological foundation in the last VI Parts of
this work and completed therein.
This is the unexpected outcome of the germination of smut spores in nutrient solu-
tions from the phylogenetic side, in the consideration of the natural classification of the fungi.
It leads to the natural valuation of the basidium and through this alone to an understanding of
how the course of morphological differentiation has taken place in the direction of the basidia.
Besides this, however, these new facts have given new and important elucidations of the
saprophytic life of these fungi from another point of view. The theory previously held, accord-
(1) We are here involuntarily reminded of TULASNE, who designated the fructiflcatiye germina-
tion in the Ustilagineae and in the Uredineae jointly, on the ground of their formal correspondence, as
germination in promycelia and sporidia. TULASNE had observed germination of these spores only in
water where no differentiation at all is shown in the promycelia of the Ustilagineae and the Uredineae.
The characteristic formal variation existing between these, however, can be determined only by culture of
of the spores of the Ustilagineae in saprophytic nutrient substrata instead of in water. Here TULASNE'S
promycelia in the Ustilagineae were first proven to be Hemibasidia in contrast to those of the Uredineae,
whose promycelia are shown by comparison to be typical basidia, Protobasidia.. As has already been
said, TULASNE suspected the natural relationship of both sets of forms, but a determination of the
characteristic differences existing between the two types was not granted him. This was first made
possible by the improved methods in the culture and investigation of fungi which I introduced and
chiefly by the fact that I broke through the conception held until then, according to which the parasitic
fungi, and here especially smut fungi, are dependent for development only on their host plants.
(2) Compare plates VIII and IX in Part V.
(3) Compare plate X in Part V.
(4) Compare plates II, III, IV and VII.
ing to which the fungi living parasitically were dependent alone upon the proper host plants for
their development, has now been completely upset. Even smut fungi, the most specific of all
parasites, have been shown to be only facultatively parasitic. Therefore all doubt is cleared away
and parasitism itself fan not be considered to be anything else than a phenomenon which, simply
aee.'inniiHlated to circumstances and more or less matured, appears in the different forms of
parasites.
The new forms, occurring in saprophytic nutrition, supplement the picture of morphologic
forms of these parasitic fungi and make of it an homogeneous whole. Aside from the mor-
phologically biological side first emphasized, the pathological especially receives now its true valu-
ation. Only in the new forms, shown in the saprophytic life of our fungi, is it first possible to
form a natural idea of how these fungi become effective as parasites. Instead of the few, weak
sprouting spores in water, new spore forms appear which mature saprophytically in unceasing
abundance and which, because of unweakened energy for development, are able to seize upon
nutritive plants and to attack them successfully.
Infection experiments with this newly acquired material of infection germs were planned
soon after its discovery. First of all three forms of host plants were chosen for the experiments,
— first, Indian millet ; second, oats ; and third, maize, together with the forms of smut belonging
to them1.
For these infection experiments with the host plants named, at first only budding conidia
were used which had been developed in nutrient solutions and kept there more than a month, con-
stantly developing and sprouting. The virulence of this material was tested and, in each case,
after budding had ceased, germination of the bud conidia which were to be used produced
strong germinating tubes. The bud conidia of Indian millet were sprayed on the sprouting
seed in dilute nutrient solution by means of an atomizer, in the smallest drops possible. This infec-
tion of the young germinating seedlings resulted in the autumn in as much as 70% of smutted
plants. For this kind of infection Indian millet is better suited than other experimental plants
because of the slow growth of its germinating seedlings and further it was here easily possible
to determine the limits within which infection is effective in the growing germinating seedlings.
Seedlings when just sprouting were proved to be the most susceptible. Susceptibility decreased
with the further lengthening of the germinating seedlings and was ended when they had grown
some cm out of the sheath. Penetration of conidia into the germinating seedling, sprayed on as
described above, was easily determined by observation, since the penetrating germinating tubes
leave a noticeably large hole at the juncture of the two epidermal cells*. The further penetra-
tion of the germinating tubes through the epidermis into the interior of the tissue may be fol-
lowed without difficulty.
With the results obtained with this corn and, in the same way with the succeeding experi-
mental plants, it was proved incontestibly that infection germs produced in artificial substrata
are most highly capable of infecting the host plants.
(1) Compare the discussions In Part XI of thin work.
(2) See the drawings on the plates In Part XL
IO
In the second object under experimentation, oats, besides the direct infection of the ger-
minating seedlings by spraying with conidia, a second form of infection was obtained by the
introduction of abundant conidia of the oat smut into good compost earth, rich in humus, and
also into well manured earth, leaving them undisturbed for some time. The young seed and
oat grains were then covered with the soil thus infected and the cultures were left undisturbed
in a place not too warm. The sprouting oat grains had to grow through this infected earth
layer and, as shown by the experiments, underwent an infection leading to 30 to 40% of smut-
ted plants, harvested later. With these experiments it was proved that the germs of infection
living in the soil and particularly in manured earth, where they developed further, can attack
the host plants and produce smut diseases as found in nature in fields of oats.
With both experimental plants, Indian millet and oats, the young germinating seedlings
are susceptible to infection by smut fungi ; in the third experimental plant, maize, infected with
the common smut, the infection experiments on young seed were without result ; only here and
there did a young maize plant become smutted or destroyed by a smut swelling. All the other
infected plants remained perfectly healthy. They developed into large blossoming maize plants
without a trace of disease. Particularly in the pistillate flower spikes of the mature plants,
the smut phenomena never occurred. Accordingly, the so universally extensive and striking
phenomena of this common boil smut in corn can not be called forth by infection of the ger-
minating seedling of the young seed, as was proved in oats and Indian millet. The parts in which
infection takes place are to be found in mature plants and could be found without difficulty in the
infection material, the conidia of the corn smut, which was acquired in unlimited abundance and
easily used. All parts of the mature plant were proved to be capable of infection, if the young
tissue of their new shoots grows sufficiently freely and near the outside. Infection could be
obtained by injection of bud conidia into the vegetative tip of the young plant as well as in young
leaves, young axillary parts and in the young staminate inflorescences, in forms almost never
observed in nature. Quite independent of these places, the embryonic cells of adventitious roots
and particularly young pistillate flower spikes, appearing ultimately, are proved to be especially
capable of being infected. The adventitious roots were transformed into thick smut swellings.
The separate ovaries of the pistillate flower spikes were similarly developed into giant smut
boils which under certain circumstances caused the whole infected spike to grow to the size
of a child's head1. It was shown in further experimental infections that only the very youngest
tissues are accessible for infection germs and that the parasite remains strongly localized on the
point at which it penetrated into the tissue. After an interval of 14 days, the formation of smut
spores occurs at this point in the tissue excrescences already formed. The same places in a some-
what more advanced condition, the tissues being already hardened, are no longer accessible for
action of the fungus. It penetrates them indeed but develops neither tissue excrescences nor smut
boils. Susceptiblity of maize to the germs of infection is found in all sufficiently young embryonic
parts of the tissue, which are accessible from without.
(1) Compare the illustrations on plates III-V in Vol. XI.
1 1
.•Icfordiinily. in the Am/,- maize plant, the matter is quite different from that in oats and
Indian millet. This plant offers the fungi germs, in the different life stages of its vegetative points,
young tissue accessible from without, — for example, in its embryonic leaf buds, young axes, in the
ailvi-mitiou> roots suppU'inenturily formed, the pistillate flower spikes etc. In oats and Indian
millet these tis-ues are shut off from the outside and are inaccessible for the germs of infection.
For this reason, the young maize plant is not attacked by the germs of infection in the young
>ee<l hut in the mature plant. The parasite which has already penetrated into the tissue remains
strongly localized in the place penetrated and every part accessible to infection, in the young
leaves, blossoms, axes and roots, must be infected by itself if the smut boil is to be produced
which at the latest appears after three weeks.
The etiology of the common smut accordingly differs essentially from that of the two
earlier cases and the manner in which infection is carried out in nature is not less different. Smut
spores which did not germinate in water, produce bud conidia in saprophytic substrata, in rich,
mouldy and well manured earth quite the same as in the translucent nutrient solutions. These bud
cotiidia very soon pass over into air conidia and it is the air conidia* which easily disseminated
through the air reach, without any difficulty, the susceptible parts of the host plant in which we
observe the appearance of smut. Further, it is conidia produced by saprophytic nutrition, and
especially air conidia, which carry out infection in nature. Entire maize plants grown for
experimental infection became smutted without exception if the infection was properly carried
out.
The experiments, as far as given in Part XII of this work, ended with these results.
Experimental infection was repeated in later years in order to obtain smut material, also, for the
purpose of instruction and produced thereby a number of additional results.
It was discovered, in experiments on maize smut, that the susceptibility of the host plant
is not limited to one part of the young germinating seedling as had been previously supposed, but
re-occurred in the most various parts of the matured plant, and that the young blossoms of the
pistillate spikes are particularly susceptible to infection from without. This discovery leads of
itself to the closely related consideration, whether this case of blossom infection, as proved for
maize smut, might exist only in maize. Evidently it is the young tissues of the pistillate blos-
soms and of the ovules which in maize can be directly attacked. In unbiased, comparative judg-
ment, nothing stands in the way of the assumption that in other host plants inhabited by smut
fungi, the ovaries with pistil and stigma, should also be accessible for infection. They too consist
indeed of young tissues which may be attacked freely in the open air by infection germs as are
the ovaries of the pistillate flower spikes of maize. If no possible cleistogamy exists in the blos-
soms they are accessible for the germs of infection from without so far as disseminated by
the air. Without doubt, a second place of infection exists here which had entirely esca|>ed
observation and had to remain so, as long as the etiology of the common smut in maize was not
known. For this reason it was possible for the previous conception, according to which the
young germinating seedlings alone could be infected by smut germs, and also that mature plants
(1) See figs. 1-9 plate II. Part XI.
12
were immune to the germs of infection, to obtain an almost dogmatic significance. Without doubt
this holds good so far as the vegetative part of the plant is concerned. However, it does not hold
good any longer, when the embryonic blossom buds appear and the young ovaries with pistil and
sigma now become accessible from without. It would indeed be remarkable if the young ovaries
in maize alone should be accessible and the pistillate blossoms in all other plants would not be
capable of being infected.
This consideration caused me soon to take up infection of the blossoms in our varieties of
grain, which, however, were resultless, since the external conditions were as unfavorable as pos-
sible for this infection. Plants infected in the open air, or in the grain fields, were injured by
birds or cut down before the seed had been harvested. It was possible to observe only the pene-
tration of the germs of infection into the young ovaries. Beyond this, experiments were frus-
trated. However, in the infected blossoms, so far as the observations were carried on, no smut
appeared that same autumn. My time being taken up by other investigations, I let the experi-
ments stop here, only to resume them later in a different place and with better resources. This
was after my removal to Breslau. It became clear from a number of preliminary experiments
that, without the assistance of a valued and experienced fellow worker and without the resources
of an experimental field, investigation in this direction could not lead to very profitable results.
I found the long wished for fellow worker in my scholar and assistant, Dr. Richard
Falck, and the Cultusministerium, at my request, generously granted the resources proved neces-
sary for carrying out blossom infection in detail. Thus more than four years ago, we began the
new investigation of blossom infection as it exists supposedly in smut fungi, and the following
results are the outcome of the work done with my young friend, Dr. Richard Falck.
BLOSSOM INFECTION BY SMUT FUNGI.
For our experiments in determining blossom infection in the host plants of smut fungi,
those forms come first and chiefly under consideration whose spores are powdery and whose
spore masses are easily scattered by the wind and thus distributed. These are, first of all, the
dilTerent forms of loose smuts which occur in our grains, — the loose smut of barley, of wheat and
of oats. The characteristically chosen name, loose smut (Flugbrand), indicates the distribution
of the spores by wind, in nature.
The spores of the loose smut, however, are not the only ones which may be considered
for blossom infection. We have seen in maize smut that the spores themselves of the spore
masses were not scattered, but that, in the germination of spores on a saprophytic soil substratum,
air conidia are formed which in the place of smut spores take over the distribution of the germs
of infection. And the results of infection experiments with maize smut have furnished the most
conclusive proof that these air conidia are at least just as effective for the infection of the host
plants.
Aside from maize smut there are still other forms of smut fungi which develop just as
diffusible air conidia, in which we must consider the possibility as to whether they too can reach
the blossoming plants by means of the air. These are, for example, Ustilago dcstrucns', and
especially the stinking smut of wheat: — forms of Tilletia. In all the cases here named, plants
are involved whose pollen is disseminated by wind and also at the same time forms of smut fungi
with similar dissemination.
Smut fungi occur, however, also in the blossoms of host plants, fertilized by insects, whose
smut spores are not disseminated like the loose smut. An especially striking case of this kind is
the anther smut of the plants fertilized by insects. On these host plants, only the anthers are
transformed into the spore masses and the spores from these anthers do not have the powdery
nature of the loose smut. The smut spores are disseminated very little, if at all, by the air, but
are held fast in the anthers, and are first forced out of these by the insects which visit the blos-
som. The fact can escape no attentive observer that the anther smut in white or light colored
blossoms ; for instance, Melandryum album and Saponaria officinalis, is betrayed by a peculiar
blemishing of the blossom head by violet smut spores. External proof is here given that insects,
visiting the blossoms, force out the anther smut as well as the pollen. They carry over the
spores of the smut as well as pollen to the stigmae of the blossoms, where conditions for their
germination and further development are to be found in the stigma secretion itself.
We will place the forms of loose smut most prominently because investigation has advanced
furthest here and the results arrived at are as forceful as they are convincing.
Formerly only one form of loose smut was differentiated, which was called Ustilago
carbo and which was thought to live in oats, wheat and barley as host plants. In the middle of
(1) See flgs. 9-12. plate VI, Part V of this work.
(2) See illustrations on plates XII and XIII, Part V of this work.
14
the 8o's, it was determined by spore culture that the loose smut of oats1 is an entirely different
form from the one existing in wheat and barley2. The loose smut of oats, when germinating in
nutrient solutions, forms chiefly hemibasidia with conidia, which continue budding indefinitely
as long as the nutrient substances of the substrata last. After exhausting the nutrient
solutions, the broken down bud conidia grow out into strong, long germinating tubes which
were never found in conidia whose spores germinated in water3. The loose smut of wheat and
also that of barley germinate with hemibasidia, to which the first conidia formed remain attached,
growing out into long germinating tubes, but free conidia never appear. An increase of the
fungus through budding of the conidia, which takes place indefinitely in the oat smut, is never
observed here. Only threads are shown which formed hemibasidia directly. They branch weakly in
nutrient solutions and develop only a relative length3. The difference between this smut form
and that of oats is so convincing that, according to my observations, the loose smut in wheat and
in barley must be taken as distinct species. The spores of the loose smut of wheat and barley
may not be distinguished from one another. Also no differentiation whatever is shown in the
germination of the spores. The question remains open whether the fungus in barley is a still
different form from the one in wheat. Anticipating the actual decision, Rostrup has designated
the loose smut of wheat as Ustilago tritici, in contrast to barley smut, to which Brefcld had
given the name Ustilago hordei.
After the natural dusting, that is, the infection of the blossom by smut spores, it is abso-
lutely necessary that the spore masses in oats, in wheat and in barley, should appear simul-
taneously with the blooming of the grain. This takes place in a most striking manner. One can
observe indeed that the spore masses of the plants attacked precede somewhat the blossoming
of the grain plants, but in any case are present at the time of completest development and are
capable of being disseminated, when the blossoms are developed and in full bloom. This
peculiar coincidence of the blossoming time of the grain and the ripening of the spore masses
of the plants attacked necessarily gives rise to the question, whether any dusting, that is, any
infection of the blossoms by smut spores, might have taken place here. And the designation loose
smut for this spore mass disseminated by the wind, has already become so significant that one is
unconsciously led to consider that there is a natural connection between these smut spores,
capable of germination, and an infection of the blossom.
(1) Compare the text and illustrations in Parts V (plates II and III) and XII (figs. 25-28, plate
VII).
(2) Compare figs. 29-32, plate VII, Part XII.
(3) 1. c. text and illustrations of Part V.
METHODS OF BLOSSOM INFECTION.
In order to carry out the experimental infection, it was necessary to work out methods
approaching most nearly the natural dissemination of the spores. That is, so to imitate the
phenomena of nature, that the easily scattered smut spores from the spore masses penetrate with
the greatest p(»xil>le sun-ness into the blossom of the grain without, however, causing any pos-
sible disturbances. For this it was necessary to observe especially that the exact period was reached
in which the blossom of the grain to be infected was most widely open, thus furnishing the pre- 7
liminary conditions most favorable for blowing the smut spores into them. Blossom infection
naturally could be carried through only in dry weather, best of all in sunny weather, when the
host plants are dry and the spores of the loose smut may be easily disseminated. After various
experimentation an atomizer of strong rubber and of suitable size was used for this. The smut-
ted inflorescences were put in it and the opening closed with a connection which ended in a tube
with a corresponding opening. Previous tests had shown that by this means the smut spores
can be driven from the atomizer in sufficient amount, most finely distributed and comparatively
powerfully. The heads or panicles to be infected were then placed in a cylinder, the under
opening of which was loosely closed with a wad of cotton, and the spores were forcibly blown
into it from the open end. After waiting a little for the spores to settle, the heads were taken
again from the cylinder. Supplementary tests of heads thus infected proved that in this kind of
infection the smut spores were actually carried into the bloom, so far as the existing condition
of the single blossoms permitted. Naturally, the number of blossoms of a head which are open
at the same time and make possible this penetration is more or less restricted, according to
circumstances. The blossoms on a head do not bloom simultaneously, they are generally most
advanced in the middle, while those to be found at the base and near the top open later. From
this it is evident that, in a single infection by thus blowing in the spores, only a corresponding
part of the blossoms of the head can be effectually infected. Thus, infection exceeding a certain
per cent may not be expected here. Several repetitions of the infection of single heads are not
advantageous, since disturbances of the normal development of the blossoms may always be
unavoidably introduced by the processes.
In nature the conditions for dissemination are incomparably more favorable. Smutted
plants, standing in grain fields, do not scatter their smut spores only once when there is enough
motion in the air, but constantly throughout the whole time in which the blossoms of the sur-
rounding heads are opening successively. Thus the probability of infection of neighboring healthy
plants increases appreciably in comparison with infection in cylinders as already descrilH-d. Rain
belongs among the chief disturbances possibly occurring during infection in nature, that is wet
weather which deprives the loose smut of its natural fate and carries its spores down on to the
soil, where they are lost for blossom infection. However, too dry and too warm weather can
also be unfavorable for infection, since it hastens very much the development and ripening of
the grain. Germination of the spores needs also a sufficient amount of moisture.
i6
For the sake of brevity, the designation "cylinder infection" will be used in the following
for the kind carried out in glass cylinders of tested size by means of the disseminating apparatus
already .described.
The second kind of infection, which supplements most naturally the one already given, is
infection by artificial introduction of the smut spores in the separate blossoms, which have just
opened or are ready to blossom. This kind of infection by artificial introduction of the smut
spores in the separate blossoms necessitates naturally more or less forcible attack upon them.
The smut spores are most expediently carried over into the interior of the blossoms by means
of a fine brush and here placed upon the stigma and ovary. To carry out this infection most
skillful hands are needed, which will not injure the further opening of the blossoms but easily
and surely, by means of the brush, will carry the smut spores over on to the stigma and ovaries
in the interior of the blossom. We have used with advantage the hands of skillful women. After
a little practice they have carried out the manipulation of inoculation with relative delicacy and
sureness. Since the infection is here carried out on separate blossoms it is more certain than in
cylinder infection and the results are also still more assured by the cutting off and removal of
all non-infected blossoms. If this is done with the greatest care and skill, it may be assumed,
that each blossom must be infected and that each ovary will be attacked by the germs of infection.
However, we find here a number of sources of error which are as natural as they are pertinent.
If separate blossoms are passed over rapidly in this infection a rather considerable source of
error is given for the later per cent of smutted plants, since only a limited number of blossoms
of a head may be infected at the same time. The second source of error is encountered if all
non-infected blossoms are not removed. Of course in this form of infection the secondary points
may be considered as disturbances which are given already under cylinder infection.
From this it is easy to understand that in infection of separate blossoms the result can
be complete only in fortunate cases and that a corresponding loss must be shown in all those
experiments where cases of error may have crept in. In any case infection of the separate blos-
soms is disproportionately surer and more effectual than that of cylinder infection, even if it is
inferior to this in the artificial introduction of spores here necessary for infection.
A further circumstance is of especial value for the success of blossom and cylinder infec-
tion. This lies in the freshness of the infection material, which in any case must be taken
directly from the field and if possible should be taken from the same field for the infection of
the plant.
Doubtless the methods of infection here used can be further and better improved. The
results given below prove, however, that they are reliable and guarantee a relatively high grade
of effectiveness.
Besides infection of the blossoms, infection of the young seedlings must be introduced in
this same experimental field. It was thought formerly but erroneously that infection would succeed
only on young germinating seedlings. In the same way it would now be erroneous to assume
that, in experimental plants, blossom infection is the only effective one. Both possible means of
infection should be kept in sight. First, infection of the young seedling; second, in the blos-
som. It is very possible that in the same plants both forms of infection can exist side by side.
17
It must tlii-n IK asked which of the two is the more effective in any especial case. Besides this a
third case is possible, — that only one of the two infection forms exists alone, either the infection
of the germinating seedlings or that of the blossoms. The experimental infection undertaken
on young germinating seedlings for supplementation and comparison cannot be made in the same
season, in summer, as are blossom infections, and for these the same favorable circumstance
does not hold good any longer, that is, the capacity for germination of fresh smut material. It
is necessary to make these experiments in spring with smut spores harvested from the field during
the previous summer and further with grain taken from the same fields, which are, however,
free from smut.
The gathering of spore material, which must remain fresh and uninjured until the next
spring, is no easy matter. The spore masses are unavoidably polluted by the air even up to the
time of ripening, they are detrimentally influenced by occasional rain and especially by insects
which creep into the spore masses, eat the spores and when possible deposit their eggs there.
Smut material gathered, without special precaution, from the attacked inflorescences of grain
will certainly be damaged in the following spring by worms, often indeed being made useless.
Very special precautionary measures and peculiar methods are needed in order to get sufficient
amounts of pure smut material in summer with the assurance that it has been protected from
all injurious influences. From a long series of experiments, the following method has been proved
best for obtaining pure smut material for infection the following spring. Spore material is
gathered in sufficient amounts, soon after the breaking open of the spore masses, before any
injurious influences have made themselves felt, and is kept eight days in a dry place. Then the-
smut spores are carefully sifted on to white paper through a fine copper sieve which lets through
only the spores. The refuse remaining on the sieve is thrown away. Experience has proved
that the smut material thus sieved can be as well kept as possible in this powdery form until
the next spring and particularly that no insects will enter the smut spores. These sieved spores
are carefully put in a number of small flasks with flat bases, which are filled not more than one-
fourth to one-fifth. The wide neck is closed carefully with sterilized paper and the spores are kept
in a cool, dry place through the winter. The preservation of spores in many small flasks has the
especial advantage that if any injurious influence is present in one small flask, the other spores
were protected from it. In fact, in this form, the material to be used for infecting germinat-
ing seedlings has shown in every case that it has been well protected so that it can be used in the
freshest possible condition. In spring, shortly before using, the spores are put in clean water and
thrown about five or six times on a centrifugal sieve. The spores thrown out quickly have been
proved to be almost perfectly pure and cultures may be made with these spores in a nutrient solu-
tion which show scarcely any pollution throughout the period of culture. The treatment of spores
in this form has the additional advantage that, by the day's retention in water necessary for the
purification of the spores, they are prepared as favorably as possible for germination, and that
spores, which are then sprayed in a dilute nutrient solution on the germinating seedling already
prepared, will germinate without loss of time in the drops sprayed on the seedling and can pene-
trate into it directly. For this infection of germinating seedlings, it is not advantageous to
use conidia which appear in spore germination and increase almost indefinitely by budding
i8
in the nutrient solution. It is less tiresome and more certain of results to carry out the infection
with smut spores instead of conidia, if they have been prepared beforehand for direct germination
in the way stated above. This use of smut spores for infection becomes indeed a necessity if
no conidia occur in spore germination when one can depend only on the use of spores, as may
occur in smut spores of barley and wheat.
The same spore material used in spraying germinating seedlings may now be used in still
a second case, in order to infect sufficiently the best compost earth. This earth was mixed in
the third case with horse manure. The spores were abundantly blown on to it with the atomizer
and mixed in and the earth thus infected was used for covering the sown grain. In the fourth
case, independent of these three cases, the grain in a dry condition was mixed with dry smut
spores and then sown.
BLOSSOM INFECTION IN WHEAT.
We will now turn to the experiments made in the last four years with forms of loose
>tmit, and their detailed results. We will begin with experiments on wheat and the loose smut
In-lunging to it, which Kostruf named Ustilago tritici. Wheat is a plant well suited for blossom
infection. The blossoms of the different varieties open differently, but the stamens generally
grow free and the openings and cracks formed between the glumes are wide enough to make
possible infection by spores. When inoculating the separate blossoms, only very little work is
necessary in order to introduce the smut spores into them by means of a brush. Care was always
taken that a larger number of spores was introduced into the blossoms in order to insure infec-
tion by this means. The stigmaf do not extend far enough out to make possible a limiting of
the infection to them alone. Since, however, there are present in the ovary itself young tissues
in themselves accessible for the germs of infection, it is not very important if the possibility
of carrying out the infection separately on the stigma and on the ovaries is very much restricted.
After infection has taken place, the single heads on which the blossoms have been infected, the
non-infected buds having been removed, were marked with colored, non-fading threads in order
to distinguish them and to make certain their harvesting when ripe, later in the autumn. A
record was kept of the single forms of infection and in it were entered at the same time minor
details, weather and air temperature. On the third or fourth day after infection some of the
infected blossoms were investigated in order to determine how the introduced smut spores had
behaved. It was possible to observe with certainty that almost all spores had germinated in
the stigma secretion, especially on the feather-like stigma itself, and that long threads extended
from the germinating spores, which had sprouted out on the stigma tissues, and were lost
among them. Difficulties arose in later observations, undertaken to follow still further the pene-
tration of the germinating tubes through the stigma, since a clear differentiation of the fine
threads of the fungus decreased gradually; thereby the growth of the tubes through the stigma
into the young ovary could not be seen with certainty. There is, however, nothing against the
assumption that the germs of infection, germinating luxuriantly on the stigma, and growing
down into it by means of their tubes, reach at last the ovaries themselves. The same may hold
good for those spores which germinate directly on the young ovary and penetrate its young
ti-siie. Nothing more than the above given details can be learned by microscopic observation.
The ripening of the young grain was watched with great care, and, when ready, it was har-
vested just as carefully. The harvested heads were kept in a dry place and hung up in loose
bags for later ripening. Judging by external appearances, from all the infected blossoms, only
healthy grains were harvested, in no single case of which a trace of smut was found.
Besides the infection of separate blossoms, cylinder infection was now undertaken in
wheat. The heads on which this was carried out were especially marked with colored threads
in order to distinguish them in harvesting. After cylinder infection, the microscopic examination
of the blossoms for introduced smut spores was not omitted, as. well as the ascertaining of their
germination on the stigma.
20
In this cylinder infection also the appearance of smut never showed in the grain heads
harvested in the autumn. The harvested grains preserved with the precautions already given
had a perfectly healthy and normal appearance. These experiments were carried out principally
on summer wheat; less often on winter wheat, as is shown in the following statistics.
The grains, harvested from infection of separate blossoms and from cylinder infection
and especially taken from different varieties of wheat, were sown in the following spring. This
was done with precautions which excluded all chances of error. The grains were sterilized with
copper sulphate solution according to Kuhn's process1 in order to kill all smut spores which might
be present on the outer surface. That this actually took place was proved by special experiments
in which smut spores were treated according to the same process and at the same period with
the same copper solution. After thorough purification they were tested in nutrient solution as to
their capacity for germination. When the outer surface had thus been sterilized, the grains were
sown in special germinating cases, a suitable distance apart. Each germinating case held about
300 grains. The single grains lay free on a substratum of sterilized vitreous sand, which cov-
ered the underlying substratum, i-2cm thick. The germinating cases were covered and put in a
cool place, the germination of the grain was watched. When the sprouting seed had grown pos-
sibly 2cm out of the sheath, the cultures were put in the open air in a protected place and then
transplanted singly to the experimental beds in the open ground. It is impossible in this kind of
treatment for any infection germs to penetrate from without to the young plants. The plants
are immune, if the seedlings have grown 2-3011 out of the sheath, as had been proved earlier
for sorghum2, the first green leaves having appeared. In this condition, assured against all
external attack of fungus germs, they are planted in the open ground, where they need protec-
tion only from frost and other injurious natural conditions. The plants already set out developed
in different years quite normally, just as did the remaining grain plants in the fields. They
seemed externally perfectly healthy and did not show a trace of disease. Only at the beginning
of the blossoming time were results of the previous infection to be seen in places where the
embryonic heads grow out of the tips of the surrounding embryonic leaves. These results are
summarized in the following tabulated survey. It is necessary here to emphasize only the fact
that in the experiments of a separate infection of the blossoms, the damaging smut increased up
to 100 per cent. The appearance offered by these smutted fields was very phenomenal ; for the
experimenter indeed a very enchanting picture, because it proves the success of his tiresome
experiments and the correctness of the train of thought previously carried out. Never indeed
have such smutted fields been seen, as shown for example in the photographic picture of
wheat, fig. 2, plate I, which proves a total infection of all the experimental plants. If in the
separate experiments all the plants did not become smutted, it may be traced back to the
sources of error already indicated which are unavoidably present in experimentation. But even
such fields, in which 5°-7° Per cent of smutted plants may be counted, give sure and unassail-
able proof of the correctness of the decision that here, in the loose smut of wheat, infection
(1) After treating 12 hours with 5 per cent coppersulfat solution at 15-20 degrees C., the seed
was washed, let stand five minutes in fresh lime water, washed again and then sown directly on the land.
(2) Compare the text in Part XI.
21
takes place in the blossom. A summary of the experiments thus carried out is added in small
print at the end of this section.
Hence if is prm'ed positively that young ovaries are directly attacked on their stigmaf by
tlu- tjcrms of infection scattered by the wind; that the smut, however, is not developed in the
same year: but that rather the ycrms of infection which penetrated into the young embryonic
fruit remain latent in the ripened grain and after the dormant period of the seed grow out in
these. r</n(i//y. TI-I//I the germination of the embryo, in order to pass over in the inflorescence to
the production of the spore masses.
The seed from cylinder infection was treated in the same way. The percentage of smut-
ted plants fluctuated between 18 and 26 per cent. In the survey at the end of the section, the
details are summarized in small print from the list of experiments which we made.
The seed harvested in the separate experimental infections was not used up entirely in
the experiments, but a part was always kept over in order to answer any subsequent questions.
The seed, obtained in autumn from a complete infection of the experimental plants, was inves-
tigated first of all microscopically, in order to prove the presence of fungus germs in the grains.
This was done without any difficulty. Mycelial threads of the fungus were found in different
parts of the grain, especially underneath the gluten cells. They were especially present near the
scutellum. In the germinating seedling, the fungus threads were more clearly distinguishable,
since the grain attacked by them and sterilized had been sown, and fungus threads appeared
clearly in the tissue cells in all parts of the sprouting embryo, from the scutellum to the vege-
tative tip. Accordingly no doubt can exist that the germs of infection, which had penetrated
into the young ovary, had remained in a purely vegetative condition here and had passed through
the dormant period of the seed. They awoke to new life simultaneously with the sprouting
germinating seedling and developed equally with this, as it grew into the mature plant. Here
it formed anew its spore masses in the inflorescences. Only the threads of the fungus whi«.h
reached the vegetative tip of the plant with its embryonic inflorescences become fertile at this
point and form spore masses. The mycelial threads in all other parts of the plant remain sterile
without fructifying. They are widely separated from one another by the growth of the plant
and are found with difficulty in the elongated internodes, but very easily in the cells of the nodes,
which are often completely filled with them'. It is possible for them to redevelop and to cause
disease in the axillary sprouts only in those cases where such sprouts are formed on the nodes,
and young tissues are developed*.
Such are the results of blossom infection by the loose smut of wheat, in contrast to which
we must now place the results of infection on the germinating seedlings of the young seed. Infec-
tion of the young germinating seedlings was tried in four different ways as stated above. l;irst
the grain was mixed with smut spores and then sown directly upon the land. The infectious
action of the smut spores clinging to the grains had to take effect here. In the second case the
young germinating seedlings were sprayed with spores which had been purified and then prepared
for germination in diluted nutrient solution. Here the contact of the germinating tubes, growing
(1) Compare illustration 7 on the first plate In Part XI.
(I) Compare text In Part XI, pages 85-90.
22
out of the smut spores, with the young germinating seedlings was direct and extensive. In the
third case the dry seed was covered with infected compost. In the fourth case, with compost which
had been mixed with one-half its volume of sterilised fresh horse manure. In the last two cases
the effect of the manured compost must have made itself felt. In order to judge correctly the
effect of these forms of infection of the germinating seedlings by means of spores of the loose
smut in wheat, we must investigate first of all the germination of the smut spores in water
and in nutrient solution. The material kept from the previous year, through the whole winter,
weakens somewhat in germinating strength and germinates only very slowly. In spore material
which is not preserved with special care no germination whatever occurs1. The germination of
the smut spores of the loose smut in wheat is not fructificative2. No conidia are formed, but
only germinating tubes which sprout from the cells of the hemibasidia. No increase of the
germs of infection therefore occurs here, not even when nutrient solutions are used. Because
of this the strength of the infection of young germinating seedlings by smut spores is more
restricted in the soil than in other smut forms which germinate fructificatively. In compost and
manured earth this made itself especially felt, since here infection can result only through the
germinating tubes of the hemibasidia in direct contact with the grain. The chances left for a
successful infection of the germinating seedlings, according to the condition of spore germination
of the material gathered the previous summer, are from the very beginning, so far as summer
wheat is concerned, strongly decreased and improbable. It is scarcely possible to understand
how smut spores from the preceding vegetative year, which had germinated weakly in the spring
or not at all, can bring about infection of the germinating seedling.
In fact all the experimental infection tried with summer wheat resulted negatively. From
all the plants inoculated as young germinating seedlings there developed only entirely healthy indi-
viduals free from smut. The infection of the young germinating seedlings remained therefore
unsuccessful even in most varied and numerous experiments, as may be seen from the following
survey printed in small type. It should not be assumed that more favorable conditions for
infection can exist in nature than were created and used in our experiments. We are there-
fore justified in drawing the conclusion that the infection of the young germinating seedlings is
little or only slightly probable in nature. We consider our experiments in this line as not yet
completed. We will continue them in the next few years and will consider further any possible,
contingencies.
The experiments in the forms given were attempted also in autumn with smut material
gathered about four months earlier, in which the germinating strength of the spores had
decreased but little. It was just as impossible to produce any smutted plants by this infection.
Therefore in the loose smut of wheat we face the fact that blossom infection is fully and
indeed totally successful and that infection of the germinating seedlings is resultless. We must
conclude from this that, in this loose smut, blossom infection is the ruling form of infection, if
not the only one.
(1) Compare the results of the investigation on germination already given in Part XII.
(2) Compare the illustrations on plate VII, Part XII.
23
COMPARATIVE SURVEY OP THE INFECTION EXPEKIMKNTS CARRIED ON WITH THE LOOSE
SMUT OP WHEAT.
A. INFECTION EXPERIMENTS IN 190J.
I. BLOSSOM INFECTION.
1. On a hot day. the 19th of July. 1902. wheat heads In full bloom were Infected In a blossoming
wheat field In Gr&bschen. The smut was taken fresh from the same field and was Introduced Into
separate blossoms by means of a brush. Blossoms Insufficiently developed were removed. In the next
year there developed from the harvested seed
220 stalks, 67.7 per cent of which were smutted.
The control field of the same wheat taken in 1902 from a field free from smut showed no smut.
2. Blossoming bearded wheat In another field was Infected In the same way. From the »eed
harvested
80 stalks developed which contained 66 per cent smutted ones.
II. CYLINDER INFECTION.
1. June 1. 1902. soon after a thunderstorm, cylinder Infection with fresh smut from the same field
was made In three different parts of a blooming wheat field In Leerbeutel. Prom the sterilized se«d
In place 1, 520 stalks were produced, of which 39.1 per cent were smutted.
" " 2, 549 " " 37.5
" " 3, 216 " " 11.6
On an average, 29.4 per cent of the stalks were smutted.
The control field, with about 1,000 plants from non-Infected seed of the same field, had only two
smutted stalks In 500.
IIL INFECTION OF THE SEED.
1. Wheat from MUnster was mixed with smut spores from the same field and sown. Out of
300 stalks developed there, none were smutted.
The control from sterilized seed of this same field had 2 smutted specimens.
I. Wheat from Leerbeutel mixed with smut spores from .MUnster furnished
280 stalks with 2 smutted specimens, as did the control also.
3. Wheat from Leerbeutel mixed with smut spores from the same field gave
250 stalks and 3 smutted examples.
In the control, one smutted stalk was found.
4. Wheat from Schlanstedt mixed with smut spores from the same field gave
310 healthy stalks, as did the control also.
IV. INFECTION OF THE SUBSTRATUM.
1. Sterilized horse manure was Infected with pure smut spores from the wheat field In MUnster,
by spraying with an atomizer, and was then mixed with two parts of compost Wheat from Schlan-
stedt was sown In the soil thus treated.
Out of 250 stalks started In germinating cases and later transplanted Into the open ground, not
one was smutted.
2. Smut spores from MUnster were mixed with compost and wheat from Schlandstedt was sown
on this substratum.
Out of 250 stalks none were smutted.
3. The same experiments was carried out as In 1 and 2 with wheat from Leerbeutel. and smut
spores from the same wheat field. This lot. as well as the control, had 3 per cent of smutted stalks.
B. INFECTION EXPERIMENTS IN 1904.
1. BLOSSOM INFECTION.
1. Single blossoms of suitable heads were Infected In a blooming wheat Held In Grabschen with
fresh dry smut of the same wheat. In two separate places.
The sterilized grains were planted In March. 1904. on sterilized sand from the river Oder. In closed
germinating cases and transplanted In April to open ground.
The grains harvested from place 1 grew
93 stalks, 31 per cent of which were smutted.
Those harvested from place 2,
120 stalks, with 58 per cent smutted.
24
Z. A variety of wheat from Grabschen which blossoms later was infected in the separate blossoms
on July 15, in three different places. Fresh smut was used, however, from the field of Schlanstedt wheat.
Young germinating seedlings from the sterilized grain were grown in March, 1904, on sterilized sand
from the river Oder, and transplanted on the 21st of April, to open ground.
Seed bed 1 furnished 169 stalks, of which 68 per cent were smutted.
" 2 " 168 60
" 3 " 267 85 '
3. Just as in the first experiments, Schlanstedt wheat was infected in July, 1903, with smut spores
of the same kind in the separate blossoms and the sterilized grains were treated as above.
Of 171 stalks thus grown, 61 per cent were smutted.
4. Schlanstedt wheat was infected on July 16, 1903, with fresh smut spores from the field of land
wheat (Landweizen) from Grabschen, the harvested seed being treated as above.
Of 160 stalks, 62 per cent were smutted.
5. On July 23, 1903, blossoming heads of land wheat were infected in Grabschen with fresh smut
spores of the same variety, which were finely divided in very dilute malt. The liquid containing the
spores was introduced with a fine brush into the separate blossoms shortly before they opened.
The harvested seed was sterilized, planted in March, 1904, on sterilized sand from the river Oder,
and transplanted April 21st to open ground. The infection was carried out in three different beds.
The seed from bed 1 developed 129 stalks, of which 81 per cent were smutted.
2 " 204 96 "
(Fig. 1, plate I, was taken from this lot.)
The seed from bed 3 developed 140 stalks, of which 78 per cent were smutted.
6. Finally, Kostrom wheat was infected in its blossoms under the same conditions as the varities
above named.
a. With smut spores from the same variety.
of 175 successfully developed stalks 51 per cent were smutted.
b. With smut spores from a field of Schlanstedt wheat;
of 53 stalks, 63 per cent were smutted.
c. With fresh smut spores from the same field which were sprayed on in malt;
of 73 stalks, 38 per cent were smutted.
In all these experiments, controls were grown from sterilized seed from the same fields. In all, either
no smut developed or an isolated smutted specimen occurred only once in a while.
II. CYLINDER INFECTION.
Wheat from Leerbeutel, just beginning to blossom, was infected in the cylinder, July 4, 1903, with
fresh smut spores from a wheat field in Grabschen. The seed was sterilized and in April, 1904, sown
directly in open ground. The infection was carried out in two different places. The seed harvested in
1904 was planted in two separate beds.
In bed 1, of 442 stalks, 19 per cent were smutted.
" " 2, " 625 " 24 "
A control of non-infected heads from the same field gave 0.4 per cent of smutted stalks.
III. INFECTION OF THE YOUNG GERMINATING SEEDLINGS.
1. Young germinating seedlings of a variety of wheat from Leerbeutel were sprayed with smut
spores of wheat from Miinster, which were just ready to germinate, and distributed in very dilute nutrient
solution. Half of the seeds grown in germinating cases were then planted on good, well-manured farm
soil, and the other half on not very fertile sandy soil.
In the good soil, 0.3 per cent of 480 stalks were smutted.
In the poor soil, no smutted example was found In 360 stalks.
2. Young germinating seedlings of Schlanstedt wheat were treated exactly as above described with
smut spores from Miinster and the seedlings transplanted to good and to poor soil. The same experi-
ments were repeated four times in the same way, from the middle of March to the end of April.
In experiments 1 and 2, out of 400 stalks planted in good and in poor soil, none were smutted.
In experiment 3, out of 240 stalks planted in good soil, none were smutted.
In experiment 3, out of 200 stalks planted in poor soil, 1.4 per cent were smutted.
In experiment 4, out of 250 stalks planted in good soil, none were smutted.
In experiment 4, out of 220 stalks planted in poor soil, 2 per cent were smutted.
25
IV. INFECTION OF THE SEED.
The unnterlllxed seed was mixed, aa In earlier cases, with smut spores so that each grain was cov-
ered with a black coating of them. The grains were sown directly on the open ground.
1. From land wheat from Grabschen. Infected with smut spores from the same field,
280 stalks developed In good soil, of which 1 per cent were smutted.
160 " " poor 2 " " " "
S. The same wheat treated as above with smut spores from a wheat Held In MUnster. gave
In good soil, 153 stalks, of which 0.7 per cent were smutted.
" poor " 200 0.5
S. Schlanstedt wheat Infected with smut spores from the same field, gave
In good soil, out of 320 stalks, no smutted ones.
" poor " " " 360 " 2 " "
4. Kostrom wheat Infected with smut spores of wheat from Orabschen, as well as from the same
variety, gave
In good soil, out of 200 stalks, no smutted ones.
" poor 150 1 " one.
Controls from the same seed, from poor and from good soil, which had, however, been sterilised,
showed no smut In the cases of Schlanstedt and KostrOm wheat, either In good or poor soil. Wheat from
Grabschen gave
In good soil, of 250 stalks, 2 per cent smutted ones.
" poor " " 100 " (they were all which developed) 4 per cent smutted ones.
V. INFECTION OF THE SUBSTRATUM.
1. Good compost was sown with the spores of the loose smut of wheat from Qrabachen, on a sub-
stratum In the germinating cases. The seedlings were transplanted April 14, 1104, to open ground.
From 200 matured stalks, 2 per cent were smutted.
2. KostrOm and Schlanstedt wheat were treated In the same way and transplanted to open ground.
(No smutted specimens whatever occurred for 200 stalks of each variety.
3. The compost which had been Infected with smut spores was mixed with fresh horse manure,
otherwise the experiments were carried out as under 1. They gave exactly the same results as under 1.
C. INFECTION EXPERIMENTS IN 1905.
I. INFECTION OF THE SEPARATE BLOSSOMS.
1. Blooming heads of a beardless winter wheat were Infected on June 16. 21 and 22, 1904, In the
separate blossoms with fresh smut from the same field. The Infection was carried on In three different
places. The harvested and sterilized seed was sown In pleasant weather, in the autumn of the same year,
(on the 7th of October), directly on open ground. The seed harvested from the four different places
was planted In special beds.
In bed 1, 256 stalks developed, of which 34 per cent were smutted.
" " 2. 267 " " •• 43
" 3, 296 '• " •• •• 33
" " 4. 230 " " " •• 16
A control of 1,000 stalks of the same wheat had only one smutted specimen.
2. The same wheat was Infected with fresh wheat smut; the spores, however, were finely divided
In water and were put In the blossoms with a brush. From the seed, otherwise treated as under 1, In the
next year
200 stalks developed, of which 14 per cent were smutted.
3. The blossoms of bearded summer wheat were Infected with fresh dry smut from the same field
In 1904 and the seedlings grown from sterilized seed on sterile sand were transplanted April 12. 1905. to
open ground.
450 stalks developed, of which 63 per cent were smutted.
A control of this same wheat had 1 per cent smutted heads.
II. CYLINDER INFECTION.
1. Blossoming summer wheat (land wheat from Grabschen) was Infected In the cylinder with
fresh loose smut of wheat. The harvested and sterilized seed was then sown In autumn of the same year,
directly In open ground.
1.750 stalks developed, of which 8 per cent were smutted.
An equally large control from seed of the same Held, but from non-Infected heads, showed
no smut.
26
2. Blossoming summer wheat was infec ted in the cylinder with fresh loose smut of wheat. In the
next year, from the sterilized seed,
2,000 stalks were grown, of which 15 per cent were smutted.
In an equally large control of non- infected heads in the same field, 4 smutted plants appeared.
C. INFKCTION OP THE GERMINATING SEEDLINGS.
For this infection seed of various ages was used from varieties in which no loose smut had appeared.
Most of the loose smut spores from 1904 were still capable of germination. They were brought to the
point of germination by soaking in water and then, finely divided in a dilute nutrient solution, were
sprayed on the plants. The germination of the seed and the spraying on the smvt spores took place at a
temperature of 10°. After 3 days the germinating cases with germinating seedlings were kept at a con-
stant temperature of 5° and, after 14 days, having developed far enough, they were transplanted into
open ground.
1. Noe wheat from 1900-1901-1902-1903 and 1904—250 stalks of each — no smut.
2. Ohio wheat from 1900-1901-1902-1903 and 1904 — 250 stalks of each — no smut.
3. Lupizer wheat from 1900-1901-1902-1903 and 1904 — 250 stalks of each — no smut.
Some comparative cases not kept in the basement, but in a warm room, at 15°-20°C. gave just the
same negative results1.
4. Young seedlings of winter wheat (land wheat from Grabschen) were sprayed in the autumn of
1904 with smut spores of the same year, the germinating power of which had not noticeably decreased.
They were treated as above.
Out of 200 plants kept over winter and matured in the next year, none were smutted.
IV. INFECTION OF THE SUBSTRATUM.
1. Seed of different ages was used as in III. The grains were sown in the germinating cases on
compost and then covered with a mixture of 2 parts good compost and 1 part sterilized horse manure,
6 cm. deep. The cases were kept a week at 6°-8°C. (being kept moderate^ damp by means of repeated
sprinkling) and then for 14 days in a cellar at a temperature of 5°.
The experiment was carried through from each of the five different years, on each of the three
varieties named above. In all 15 cases the results were negative.
2. Finally the same substrata were mixed in the way given above in the autumn of 1904 with
spores of the same year whose germinating power was still unweakened and in them were sown grains
of winter wheat from a field free from smut.
Of the plants kept over winter and developed in the next year none were smutted.
(1) The temperature in the small ro oms (Gopperstr. 4) was regulated during the night by a lighted jet.
BLOSSOM INFECTION IN BARLEY.
We now turn to the experimental infection with the loose smut of barley1. The smut in
its outward appearance and in the form of its spores cannot be distinguished from that of wheat.
Blossom infection of the barley plant cannot be carried out so easily as that of wheat. In
only a few varieties of barley do the blossoms open in such a way that the stamens protrude.
In most cases they remain enclosed in the blossoms, that is, inside the glumes, which, how-
ever, are wide enough open to make possible a dusting on of the spores. In infecting the
separate blossoms of barley the period must be exactly observed in which these are the widest
open, because at this time the introduction of the spores can best be carried out. In any case the
attack which must be made on the blossoms for this purpose is much greater than in wheat, and
it i- self-evident that by this means an impediment to infection is caused. For cylinder infection
only the splits are to be taken into consideration which are found naturally in the blossoms.
Here too artificial infection is, under certain circumstances, less easy than wheat. As above, for
the separate infection, only infected blossoms are left standing, all others are removed and
the single stalks marked with colored threads. This last was done also in cylinder infections.
The ripe grain was collected from both series of experiments, kept dry during the winter,
sterilized in spring and sown on sterilized vitreous sand, just as was stated for wheat. As might
have been supposed, the results of the infection of the separate blossoms were, on an average, not
so favorable as those of wheat. Nevertheless, we obtained here, as may be seen at the end of
this section from the subjoined comparative survey of our experimental infections, a high per-
centage of smutted plants, even up to total infections. (Fig. i, plate i.)
As shown in the survey, cylinder infection also gives somewhat poorer results than was
the case in wheat. At the most they did not exceed 20 per cent. In the separate varieties of
barley used for this infection, fluctuations were found, as may be seen from the survey. On
the whole, however, the result of blossom infection was approximately as favorable as that
with the loose smut of wheat and, favorable conditions being taken for granted, it can be assumed
here with certainty that blossom infection is always successful if the smut spores succeed in get-
ting into the blossom.
Infection of young germinating seedlings was carried out in the same four ways as with
the loose smut of wheat, with much the same negative result as was obtained with wheat. In all
these experiments healthy plants free from smut were formed. In the comparative survey are
summarized the series of experiments and their results. Accordingly it holds good for the loose
smut of barley, as was said above for that of wheat, that the infection in the blossom is the pre-
dominant form of infection of the host plants, if not the only one. Also the anatomic conditions
1. The loose »mut of barley, concerned here, must not be. confused with the covered smut which
also occurs in barley, but does not become dusty and remains enclosed In the beard. This smut form, as
1 have proved by cultivation, differs essentially from loose smut. The spores germinate fructlflcatlvely
and form conidla. which Increase unceasingly In nutrient substrata, in the form of yeast. RO8TRUP has
designated this form, from Its external constitution, as U»t. Jcnsenii.
28
in the dormant seed, as in the sprouting seedling, did not differ from those already given for
wheat.
COMPARATIVE SURVEY OF EXPERIMENTAL, INFECTION CARRIED OUT WITH THE LOOSE
SMUT OF BARLEY.
A. EXPERIMENTAL INFECTION IN 1903.
I. BLOSSOM INFECTION.
Only a little seed was harvested from the blossom infection of 1902. This small amount failed com-
pletely when sown.
II. CYLINDER INFECTION.
1. On June 18, 1902, cylinder infection was undertaken in Grabschen on a field of barley just
beginning to bloom. In the middle of the heads chosen a few blossoms were open. From the harvested
seed
1,590 stalks were grown, of which 10.5 per cent were smutted.
A correspondingly large control with seed from the same field from non- infected heads showed
0.1 per cent smutted.
III. INFECTION OF THE YOUNG GERMINATING SEEDLINGS.
1. The young, just sprouting seedlings of barley from Munster were infected by spraying with
smut spores from the same field. The smut spores had been brought to germination by soaking in water
and were then finely divided in dilute nutrient solution.
Of the 200 stalks transplanted in open ground, 1 per cent was smutted.
In the control no smutted stalks were produced.
2. Two-rowed barley treated as under 1 gave no smutted specimens. The same was true of the
control.
IV. INFECTION OF THE SEED.
1. Five different varieties of barley were mixed with smut spores, which had been taken from a
field of each separate kind, and were sown directly on the open ground. From each of them 300 stalks
were grown. The production of smutted stalks was exactly the same as in the controls produced from
sterilized seed.
B. EXPERIMENTAL INFECTIONS IN 1904.
I. BLOSSOM INFECTION.
1. Land barley (Landgerste) from Minister was infected in 1903 in the separate blossoms with
fresh barley smut spores from the same field.
a. Before blossoming.
b. Just when the heads were blossoming.
At the end of March, 1904, the sterilized grain was sown on sterilized sand from the river Oder in
closed germinating cases. On April 22, 1904, the young seedlings were transplanted to open ground.
a. From the grains infected before blossoming
104 stalks were developed, of which 17 per cent were smutted.
b. From the grain infected during blossoming
350 stalks were developed, of which 60 per cent were smutted.
The control from sterilized seed from non -infected heads of the same field gave no smutted speci-
mens in 300 stalks.
2. On June 30, 1903, heads of a two-rowed Hanna barley just blossoming were infected in the
single blossoms with fresh smut spores from the same field. The seed was sown in 1904 as given under 1.
300 stalks were developed, of which 57 per cent were smutted.
A control of sterilized seed from non-infected heads of the same field gave no smutted specimens in
250 stalks.
3. Land barley from Grabschen was infected on July 1, 1903, in the separate blossoms, with smut
spores from the same field.
a. Shortly before_ blossoming.
b. From heads just blossoming.
The sowing in 1904 resulted in,
a. 85 stalks, of which 30 per cent were smutted.
b. 162 ' 78
4. Land barley from Orabichen was treated on July 3. 1908. as under 3b, but the fresh smut had
been taken from a field of Hanna barley. The seed, harvested from the Infected blossoms and sterilised,
was sown, giving In
160 stalks. 86 per cent of smutted ones.
5. A variety of barley from Qrabschen was Infected In the separate blossoms on especially favor-
ably developed heads with fresh barley smut from the same field. The smut was shaken up In the dilute
nutrient solution and put on with a brush. Sowing of the Infected grain, carried out as before, resulted
In 1904 In
180 stalks, which with one exception were all smutted.
(Figure 1. plate 1.)
The control of SOO stalks from non-Infected heads of the same barley had 2 smutted specmens.
6. A two-rowed, small barley, which had never had loose smut and whose blossoms always remained
closed, was Infected June 30, 1903, with fresh smut spores from a field of Hanna barley just as the
stlcimi In the artificially opened blossoms had fully developed. The grains obtained from the Infected
blossoms were sown In 1904 as described above. Of
160 stalks, 77 per cent were smutted.
II. CYLINDER INFECTION.
1. Blossoming barley from MUnster was Infected In the cylinder with fresh smut spores from the
same barley field In Grabschen. The sterilized seed was sown In April, 1904, directly In the open field.
600 stalks were developed, of which 12 per cent were smutted.
A control of 500 stalks had only one smutted specimen.
2. Blossoming barley heads from a field In Qrabschen were Infected In the cylinder early In July,
1903, with fresh smut spores from the same field. The sterilized seed was sown on April 6th, directly
on open ground
400 stalks were developed, of which 20 per cent were smutted.
A control of 400 stalks from non-Infected heads of the same field had 1 per cent of smut.
S. The blossoming heads of Hanna barley were Infected In the cylinder In the beginning of June,
1903. with fresh smut spores from a barley field In Grabschen. From the sterilised seeds were grown
In 1904
200 stalks, of which 9 per cent were smutted.
A control of just as many plants had no smut.
in. INFECTION OF THE YOUNCt GERMINATING SEEDLINGS.
1. A variety of barley from MUnster. one from Grabschen and Hanna barley were planted In soil In
germinating cases and the equally developed young germinating seedlings were sprinkled as given above
with smut spores from the same field, still capable of germination. Of each variety
600 stalks were developed, of which 1 or 2 specimens of each were smutted.
IV. INFECTION OF THE SEED.
Besides the barley from MUnster. Grabschen and the Hanna barley, a fourth variety was mixed
with smut spores and sown partly on well-manured farm land, partly on unfertile sandy soil. In each of
the 16 experiments
200 stalks developed, among which there occurred only occasional smutted specimens.
Entirely similar results were obtained In a corresponding: control In which sterilized seed had been
used.
V. INFECTION OF THE SUBSTRATUM.
Four different varieties of barley were grown In germinating cases, partly on good compost, partly
on a mixture of compost and fresh horse manure. The compost as well as the mixture with horse manure
was Infected abundantly with spores of the loose smut of barley. The seedlings germinating In this
substratum and developed further were transplanted later to open ground and of each
200 stalks were grown. They were all free from smut.
<• EXPERIMENTAL INFECTION IN 1905.
I. BLOSSOM INFECTION.
1. Blossoming land barley In Grabschen was Infected In June, 1904, In the separate blossoms with
fresh dry. loose smut of barley, simultaneously on two different fields, by three women. The sterilized
seed was grown In 1905 In closed cases on sterilized sand, then planted out In two separate beds.
30
In bed 1, 600 stalks developed, of which 58 per cent were smutted.
" " 2, 660 " " " " 44
Equally large controls of the same barley had no smut.
2. Blossoming barley from another field was Infected on June 28, 1904, with fresh barley smut, in
two different places as under 1. The smut spores were shaken in water and put into very dilute nutrient
solution. The harvested seed gave in the following year
In bed 1, of 250 stalks, only 13 per cent smutted ones.
" •• 2, " 200 " " 16 "
The control had no smut.
3. The blossoms of a two-rowed cleistogamous barley which had never had smut were infected in
June, 1904, with fresh smut of a barley (land barley from Grabschen). The following year
250 stalks developed, of which 30 per cent were smutted.
II. CYLINDER INFECTION.
1. In a barley field in Grabschen, shortly before blossoming, the still closed blossoms were infected
in two separate places on June 22, 1904, in the cylinder with fresh loose smut of barley. The sterilized
seed was sown in two different beds.
In bed 1, 540 stalks were developed, of which 9.5 per cent were smutted.
•• " 2, 670 " " " " " 9.7 "
2. The same barley was later infected in the cylinder, shortly after it had bloomed.
500 stalks developed, of which 12 per cent were smutted.
A control of the same barley had no smut in 2,000 stalks.
III. INFECTION OF THE GERMINATING SEEDLINGS.
Seed of different ages was used on fields in which no loose smut or very little had been observed.
Most of the smut spores used in 1904 were still capable of germination. The experiments were carried
out exactly as was described for the experiments of the germinating seedlings in wheat in 1905. There
were used
Probsteiner barley from 1900-1901-1902-1903 and 1904,
and Chevalier barley from 1900-1901-1902-1903 and 1904.
In all ten experiments no smut appeared.
IV. INFECTION OF THE SUBSTRATUM.
The experiments were carried out with the varieties named under III, exactly as was described for
wheat in 1905, in the same place. Here, too, no smut appeared in all ten experiments.
From the experiments with loose smut in wheat and barley, which thus correspond
exactly, the infection of the blossom has become a scientific fact. The smutted appearance due
to the loose smut in the grain fields of wheat and barley has brought forward a newly discovered
form of infection of which no one had thought before. The infection of the young germinating
seedlings which had previously been considered as the only active one, can count for little,
perhaps for nothing at all, in comparison with infection of the blossoms. The new fact is of itself
of high scientific value. Its characteristic nature is first shown by the fact that the infection in
its greatest action is entirely withdrawn from observation. The germs of infection tvhich pene-
trate to the young ovaries remain hidden in these and even until complete ripening do not
develop fructificatively, nor indeed even at the very point where the smut masses are otherwise
always and solely formed. Not one trace may be seen outwardly on the infected and harvested
seed of any smut infection which has already taken place. The anatomic condition proves that
smut spores are present in the seed and remain quiet during its dormant period. The infection
is temporarily interrupted by this dormant seed period and, after this is passed, is continued with
the further development of the plant. Only in the germination of the seed can the fungus develop
further, in order later, at the time of blossoming, to cause, as if by a stroke of magic, the appear-
ance of spore masses in the plant which, until then, had seemed healthy. The adaptation of a
parasite to its host plant appears here unth a completeness not known in any other case in the
plant kintjdom. Infection extends back to the first embryonic parts of the young plant and the
appearance of disease becomes externally noticeable only in the second vegetative period in the
last stages of development.
One would naturally think this inheritance, if the infection of the blossoms were not
proved with certainty and traced back to the time of the infection and fruiting of the embryonic
parts of the young embryo in the ovary of the blossoms. These facts, as noteworthy as they
are important for the biology of smut fungi from a purely scientific side, adjoin the not less
important results which are furnished by blossom infection for the practice of the agriculturist,
that is, for the struggle against smut fungi.
It has been definitely proved by blossom infection that smutted individuals in the blos-
soming grain field form the centre of infection for the plants and of the further distribution
of the smut. The spores are disseminated as dust from the spore masses of the plants attacked
and are driven by the wind directly on to the blossoms of the surrounding plants. They thus get
directlv into the bl-ossoms and on the stigma, where they infect the young ovary, susceptible to
infection. Only in the following year, however, do the phenomena of smut develop from the
seed thus infected as we find them in the fields.
Formerly smutted plants had been observed attentively only from one point of view. It
was thought then that the smut spores were driven on to the surface of the surrounding grain
and on the soil, and that infection in the soil came to full maturity in the germs of the seed only
subsequently and only in them. The possibility of blossom infection, in which smutted plants
represent a direct and immediate centre of infection for the surrounding healthy plants, had not
been considered at all, nor especially that the seed already harvested could have been attacked by
germs of infection from the preceding blossoming period.
In connection with the assumption of an exclusive infection of young germinating seed-
lings it was the firm belief that the struggle against smut could be successful only if the seed
with the spores clinging to its outer surface was disinfected with sterilising material, thus killing
the spores on this surface. Of what value is disinfection and sterilization of the seed grains now
if the grain is infected in the blossom? Evidently none at all. It is not necessary to kill the
spores clinging to the outside by sterilization ; for, as we have proved, they do not penetrate
into the seed. The germs of infection existing in the seed, which had penetrated at the time of
blossoming, can not, however, be killed by sterilization. This disinfection is only an external
one. Sterilization is therefore useless for the forms of loose smut in wheat and in barley. It has
already been shown that sterilized grain infected in the blossom has produced entire fields of
smutted plants.
The fact here made clear that smutted plants grow from sterilized seed of wheat and of
barley is in itself not new. It has been known to the practical agriculturist for a long time
from experience, but its correct explanation had not been found. Further, investigations were
directed into a wrong channel, since it was always assumed that the form of sterilization was
32
insufficient and incomplete if, as experience showed, smutted plants could grow from sterilized
grain. The different statements concerning new methods of sterilization and their effectiveness
are the natural results called forth by this erroneous course of thought. If the study of the
phenomenon had not thus been carried on from one point of view alone, the question would
have been considered from the opposite one ; that is, whether we had learned enough of the
way in which infection through smut fungi takes place, or whether the assumption, that infec-
tion is limited only to germinating seedlings, is far reaching enough.
Until most recently, investigations of smut infection were carried on with the assumption
that infection takes place only in young germinating seedlings. The percentage obtained in
different experiments on smutted plants may be traced back to the previous blossom infection.
The germs of infection were already present in the seed which was thought to have been
infected by the sprinkling on of spores, as, for example, in the experiments made by Otto Rose
in Rostock, on which he reported in his inaugural address, Rostock, 1903, "Der Flugbrand der
Sommergetreidesaaten und Massnahmen zur Bekampfung dieses Pilzes in der landwirthschaft-
lichen Praxis" (Loose smut of the seed of summer grains and regulations for fighting this
fungus in agriculture). We repeated the experiments with different varieties which in Rose's
experiments had given the highest and lowest percentages of smutted heads. The seed material
obtained from the same source was partly sprinkled with spores, partly disinfected, and sown
the end of March in the open field. As is evident from the following table of experiments
made with different varieties of barley, the results were the same in both cases. The average
temperature in the first three weeks after sowing was somewhat lower than in Rose's early
sowing. Our later work will throw light on the question of the conditions causing the different
results in Rose's early sowing, and in his late one.
Percentage of smutted stalks in
Barley varieties. Sterilized Seed Seed mixed with Smut
1. Bestehorn's 0.5 0.5
2. Bestehorn's Kaiser o o
3. Chevalier 3 3
6. Golden Drop o o
5. Greek, six rowed o o
7. Hanna o 0.5
8. Imperial, loose o o
9. Imperial, irregularly arranged 2 o
12. Mandschurei o o
II. Moravian i J
13. Naked, small blue o o
14. Naked, large, 2 rowed o o
16. Naked, 3 forked Neapolitan o o
17. Oderbrucher 0.5 0.5
19. Probsteiner o o
18. Phoenix v. Thillau o o
20. Rice or Fan ( Kiieher) o o
Ji . I Hack Barley o O
4. Krfurter. white O o
10. Kallina 0.5 0.5
15. Naked, 3 forked, 3 rowed 2 2.5
The discovery that loose smut does not disappear from the fields of grain in spite of
Merilization indicates convincingly that, l»esi:les the infection of the young germinating seed-
lings, still another form of infection must exist for our smut fungi, from which an explanation
could be deduced for the fact that smutted plants grow from sterilized seed grains. This fact
.>nly now been made clear and in such a natural and simple way that every agriculturist
must be interested in learning that the smutted individuals of a field are the direct centres of
infection. The germs of disease are carried directly at the time of blossoming from these dis-
eased plants to the healthy ones.
But this explanation woula be only one-sided and not very satisfactory for the agricul-
turist, if it were not possible to set up a different method for fighting the appearance of smut.
instead of considering sterilization of the grain in fallible which had been universally assumed to be
effective. And what can be the nature of this new protective means of preventing smut ? Clearly
it is no other than that the field be prepared only with healthy seed taken from fields free from
-unit and that thus the struggle against smut be undertaken not positively but negatively. It
.ircely practicable to pull up smutted plants from the field in order to prevent blossom infec-
tion. Seed must be chosen from fields free from smut and thus prevent the sowing of seed
uniins already attacked by the smut infection. Pure seed from fields free from smut must from
now on be the means of ending the agriculturist's strnyyle ayainsl smut. If this is universally
and carefully carried through the appearance of smut must of necessity decrease gradually and
cease entirely so far as forms are involved which are infected in the blossom.
With this, our investigations of blossom infection in the loose smut of wheat and of
barley are concluded for the present. A subordinate question must not remain unanswered
here, — which involuntarily becomes obvious, — the question namely, whether the smut germs of
infection found in seed infected in the blossom can remain capable of development for several
years. The solving of this problem strengthens at the same time the certainty of the fact that
infection takes place in the blossoms and that the germs of infection exist latently in the ripened
seed.
A part of the wheat and barley seed which had been harvested was retained and used
for experiments in succeeding years. N'ew sowings were made, once of wheat and once of barley,
from the seed grain from which in the first year, after successful sterilization, the highest per-
centage of smutted plants were produced, but which had lain dormant two years. The seed
was sown with all possible care as given above and. from the grain which proved itself still
capable of germination, strong plants were grown which, at the time of blossoming in the second
year, gave the same picture of smutted experimental fields as described in the first years and
reproduced in figs, i and 2. All the plants in the separate experiments were smutted. By
means of these last experiments it u-as proved to be a fact that the germs of infection latent in
34
seed remain capable of development through the period of two years. This result justifies
the assumption that the capacity for development can last even as long as, perhaps, much
longer, than the germinating capacity of the seed itself. To continue the experiments further
in this direction would have only scientific and no practical value, since seed more than two
years old is never used in practice.
A second subordinate question must not remain unanswered here which is furnished by
the external, almost complete, correspondence between the loose smut of wheat and of barley.
The question, namely, do two different forms exist here or is the same smut concerned in the
attacks on the Hordeaceae, that is Hordeum and Triticum? The detailed cross-infection of
barley smut on wheat blossoms and wheat smut on barley blossoms has not yet given sufficiently
convincing results. It is,__however, not impossible that the very dry summer of the preceding
year influenced the infection of the blossoms. Experiments have been begun again from the
beginning and it should be possible later to report results concerning this.
35
THE INFECTION OF OATS.
A third form of loose smut must now be considered in connection with those of wheat
and harli-y. that is, of the Hordeaceae. This is the one appearing on oats; that is, on the
.1; vi/ci. -,-()<•. Externally this smut resembles the earlier forms in its spore masses and the form
of the spores. When cultivated in nutrient solution, however, these smut spores soon show great
differences. The loose smut of oats does not germinate stcrilely, but fructificatively1. Conidia
of a definite form are formed from the licmibasidia by direct budding; these form a highly
characteristic species of bud conidia, the broken-down members of which grow out at once to
-tr.mg, long germinating tubes*, when the nutrient solution has been exhausted. These tubes
will penetrate into the host plants. To the difference in germination is added now a second
difference, that of the period of germination of the spores. This does not end. as in the two
other forms, with the lapse of a year. It continues for several years and the spores, investi-
gated then as to their germinating strength, germinate just as strongly as those freshly gathered.
It is evident that in this smut form we are concerned with spores which, by the energy
of their development and the unceasing increase of their conidia in saprophytic substrata, show
a power of infection not possessed by the loose smut of wheat or of barley. The latter depend
for their infection on young blossoms ; that is, stigma and ovule, and have been proved ineffective
for the inoculation of young germinating seedlings in the soil. The behaviour of the oat smut
takes the opposite course of action ; namely, the inoculation of young germinating seedlings,
which is considerably favored by the increase of the germs of infection in the earth.
Inoculations made earlier with loose smut of oats and reported in detail in Part XI of
this work5, have shown that undoubtedly the infection of young germinating seedlings takes
place here. The effect of the germs of infection sprayed on the young germinating seedling
with an atomizer showed that no total infection was obtained by these circumstances, — needing
closer investigation, — but only a result of from 7-20% of smutted plants. The experiments,
however, with infected compost and with humus soil, mixed with one-half its amount of horse
manure and used for covering the seed grain, gave a percentage of smutted plants which had
been increased up to 30-40%.
The results obtained previously were repeated in numerous experiments made in success-
ive years, and particularly in the last five. They furnished no better results from inoculation
with the atomizer, but in experiments with humus soil and manured garden earth, they increased
to more than 60%. A number of subordinate circumstances are present here which favor infec-
tion, among them especially the longer development of the germs of infection in the humus
soil and manured garden earth here used for covering the seed. Probably a delayed develop-
ment in the germination of the seed is here beneficial to the germs of infection. But investi-
(1) See plate II, Part V of this work.
(2) See plate III. Part V of this work.
(1) 1. c. page 28.
36
gations, fluctuating as yet in their results, have not been worked out sufficiently. They will he
reported in a statistical survey in the next work on smut fungi.
To determine the influence of temperature, experiments were made on the germinating
capacity of smut spores and seed grains at constant low temperatures. It was proved that smut
spores can germinate in nutrient solution almost at the point of freezing. Germination is thus
only relatively delayed, otherwise it is just like that at higher temperatures. However, the seed
germinated also at low temperatures, almost down to zero, but very slowly. If spore germina-
tion and germination of the seed, is proportionately delayed here by lowering of the temperature,
it is not possible to understand how effectiveness can be obtained by cooling. Yet some effect
will appear if germination is increasingly delayed in older seed, but not to the same extent in
the smut spores. It is not advisable to use too low a temperature for experimental inoculation,
since development will only be prolonged ; on the contrary, it is questionable whether differences
of temperature in infected earth and in sprouting grain can favor infection. Further experi-
ments on this have just been made; they were very much impeded, however, in their exact carry-
ing out.
The first experimental infections with the loose smut of oats on the blossoming grain could
be made only two years ago. Inoculation of the separate blossoms is possible in this case
only with very appreciable interference with and destruction of the blossoms. The time in which
the oat blossoms open can be determined only with difficulty and an artificial opening of the
blossoms necessitates a separation of the glumes, which are tightly closed. A high percent-
age of the harvested oat grain from a blossom inoculation was barren and a considerable
number failed in germination, probably as a result of the disturbance due to the mechanical
injury made during inoculation. The grains ultimately germinating were shown to have weak-
ened in germinating power and most of them withered subsequently. It must be added here
that wire worms appeared in the beds and destroyed all that were left, excepting a few plants
from which healthy plants were finally developed.
Cylinder inoculation of the oat blossoms with the atomizer was then carried out. Most
of the blossoms of the oat panicles which hang downward were infected from below with smut
spores by this cylinder method of dissemination. The harvested seed, however, exclusive of
some isolated smutted plants, has resulted as yet only negatively.
From the results obtained in inoculating the blossoms of oats with the loose smut, we can
indeed draw no final conclusion as yet, but can say this much : — that blossom infection must be
only of lesser significance here ; and that, on the other hand, infection of the germinating seed-
lings in the soil, according to results already reported, is so much the more successful. There
are, however, a number of experiments where, according to our experience, the occurrence of
smutted plants scarcely makes possible any other explanation than that blossom infection must
also take place here. The circumstance that the blossoms of the oat panicle do not stand
upward, but hang downward, is not so favorable for direct inoculation of the blossoms in nature
by smut spores. The disseminated spores are not driven from below upward, but from above
downward.
37
It is worth notice that the results of infection, which we obtained, are thus connected
naturally and harmoniously with the appearances displayed in the germination of spores,
especially on saprophytic substrata. The increase of the germs of infection in soil, especially
in manured earth, indicates a predominant infection of the germinating seedlings. The note-
worthy fact aU<> that the spores of the loose smut of oats have retained their power of germi-
nation for many years and that they can 'remain capable of infection for a long time in the
earth indicates also an infection in the soil.
The different results obtained here, on the one hand with loose smut of the Hordeaceae, on
the other hand with that of the Avenaceae, should prevent the laying of too strong emphasis on
any single factor of infection. Externally the loose smut of oats does not differ essentially
from the other two forms. In its biological behavior is first shown the dissimilarity which would
have escaped observation when judging only by the character of the loose smut, as was done
earlier.
BLOSSOM INFECTION IN MELANDRYUM.
The smut forms already described appeared in the blossoms of grasses; that is, of plants
characterized by wind fertilisation. There are, however, a number of smut fungi which occur
in plants fertilized by insects and which attack separate parts of their blossoms. An especially
characteristic form of this kind is given in the anther smut, which appears chiefly in the blos-
soms of the Caryophyllaceae. The infected host plants appear externally absolutely normal,
the anthers alone are attacked by the smut fungus, Ustilago antherarum or Ustilago riolacca1.
Instead of pollen grains, as in normal anthers, thick spore masses with violet spores are
found in the pollen sacs here. The spore masses are very abundantly formed and pushed for-
ward from the place of formation in such quantities that the anthers rupture, exposing the
spore masses. The spores are not as dusty nor as easily disseminated as those of the loose
smut. They have a rather sticky nature, such as belongs to the pollen of plants fertilized by
insects. If, for example, the blossoms of hlclandryum album infected with anther smut are
observed for several days at the beginning of their time of flowering, it will be seen that influ-
ences are felt here which force the spores out of the anthers. The white inflorescences look as if
soiled by clinging smut spores. It is by this means that anther smut usually makes itself known
outside of the attacked blossom. The blossoms of Melandryum album open in the evening and
remain open in the dark. They are visited by insects, especially night-flying butterflies, which
stick their probosces into the blossoms, in order to suck the honey. In this way spores of the
smut are forced out simultaneously, thus soiling the white inflorescences with the dark smut
spores. When convinced of this fact, one understands involuntarily that the forcing out of
the smut spores from the anthers of the infected blossoms is brought about by the butterflies.
The infection, that is, the distribution of the smut disease, therefore is not brought about here
by the wind, but by insects which fertilize the blossoms. The insects which have visited a
smutted blossom carry over to the stigma, the style and the young ovule of neighboring pistil-
late blossoms, the smutted spores sticking in masses to their probosces, so that infection can
take place by means of insects in the simplest and most natural way from staminate blossoms
to pistillate blossoms in these dioecious declinous plants. If the investigator assumes the
role of this insect and carries the anther smut to the pistillate blossoms as does the proboscis
of the butterfly, he is easily convinced that the smut spores, carried to the inner parts of the
pistillate blossom, where they come in contact with stigma secretion and honey, the most favorable
substrata for their saprophytic nutrition, germin ate most easily here and indeed in the forms
described for anther smut in Part V of this work. Nothing stands in the way of the hypothesis
that the germ tubes, growing out from single or fused conidia and resembling pollen tubes2
strikingly in their form, can like these grow through the canal of the style, penetrate into the
ovule and, reaching the eggs on the central placenta, can infect them there. Like a flash of
(1) Undoubtedly the whole plant Is here attacked by the fungus of the Anther smut, which occurs
constantly on all blossoms of the much branched plant.
(2) Compare the illustrations on plate I, Part V, of this \t'ork — figs. 25-27.
39
lightning the thought comes in this hypothesis that in the stigma secretion and in the honey
of the blossoms the natural saprophytic substrata are given in which the smut spores germi-
nate, an- propagated, and penetrating with their germinating tubes through the canal of the
style, reach the embryonic seed. Here again we find an obvious explanation for the facultative
parasitism already indicated and for the first exceedingly easy nutrition of smut spores in all
possible nutrient solutions. Substrata for the saprophytic nutrition of these fungi are found not
only in tlie soil but also in the blossoms of plants fertilized by insects which are very often
attacked by smut fungi. The anther smut of these has as yet been brought forward as one,
and indeed as the most pregnant and interesting case for our investigation.
Having discussed these preliminary questions we will turn now to the practical experi-
ments. These experiments were carried out first of all with Melanttryum album. The pistil-
late blossoms of these plants were infected with the smut dust from the anthers of staminate
blossoms'. A suitable brush was substituted for the insect proboscis and the dissemination,
that is. the infection of the stigma, was carried through even to the deeper parts of the ovule
just as the introduction of the spores is thought to take place by means of the insect proboscis.
That infection had taken place was undoubted, but unfortunately the harvesting of seed from
the infected blossoms was frustrated. Plants of Mclandryum album were to be found only
outside of Breslau. Therefore inoculation could be made only here and the infected plants could
not be constantly observed. They had been cut down when we wanted to harvest the seed.
In order to avoid experiences like these, healthy and infected Melandryum plants were grown
in the experimental garden. Inoculation could be carried through in the garden and the plants
constantly watched. Unfortunately new disturbances became apparent here which could not
have been previously suspected. When the capsules had become ripe, it was seen that, except
for a small remnant, all of the seed had been eaten up by maggots. This remnant was sown
in the following year. Among the plants thus grown was found a number of smutted indi-
viduals. Further experience showed that a natural infection can be obtained with certainty, by
means of butterflies, when healthy pistillate plants of Melandryum are grown in immediate
proximity to smutted stalks. Even microsco pic investigation of the stigmafB in these plants
showed that almost without exception they had been dusted over with smut spores, which
observed microscopically, may be seen to germinate on the stigma and to develop further. The
seed subsequently harvested from such pistillate blossoms and sterilized, but which neverthe-
less was strongly injured by insects, furnished as much as 20% of smutted plants in the sep-
arate hosts. Their diseased condition could be explained only by the previous infection of the
blossoms. We must be satisfied for the present with these details. Investigations like these
cannot be completely exhausted in a few years, they need to be continued for many years if
they are to furnish results sufficient for all time.
(1) In the vicinity of Breslau. we have found only staminate blossoms which had been attacked In
the anthers by Ult. Antherarum. It has been stated, however, by older authors (TULASNE. GIARD,
MAGNIN and others), and held until most recently, that there are also androgynous blossoms. From this
It is assumed that the development of these anthers which are always smutted Is brought about by the
Influence of the fungus.
40
In any case it is of the greatest interest that the two types of inoculation may be found
in the smut forms living in blossoms which are determined on the one hand, by the pollenation
of plants fertilized by the wind, on the other hand, those fertilized by insects. The fact must
be especially emphasized here that the different formations of the smut fungi on saprophytic
nutrient substrata as shown in so many cases in Parts V and XII of this work1, may be har-
moniously connected with the infection forms of smut fungi which have now been made known.
(1) Compare the plates in Parts V and XII.
INOCULATION OF WATER PLANTS.
As a concurrent supplement of the above described infection by wind and by insects^
water must further be added as a medium and means of infection with smut fungi, which should
be taken into consideration in separate cases. The forms of Doassansia inhabit mostly the
leaves of water plants : for example, Alisma, Sagittaria etc., and develop in these strongly local-
ized pale spots, in which may be found the threads of the parasite and, especially at the end of
development, the large peculiar masses of spores by which the Doassansia forms are charac-
terized. These spore masses consist of fructificative forms only in the inner cells. The outer
>pi>re layer is sterile and forms an envelope about the inner spore mass, which thus appears as
a morphological entity. These enveloping cells lose their contents in time. These are replaced
by air and, when this has taken place, the outer spore-layer becomes a floating apparatus. The
spore masses germinate in water like Tilletia1. They produce hemibasidia from the separate
spores of any mass, on the tips of which, like little heads, is produced a number of conidia.
I'lu-se continue their budding directly and form many filiform bud conidia, both when nour-
ished in nutrient solution and also in water which is not too poor in organic substances. The
conidia are formed in great masses. They are separated from the filiform bud colonies into
ilistinct members, which are distributed in the water and can continue their budding even on
the upper surfaces. The conidia evidently reach the young leaves which are still submerged,
penetrate either under the water or on its surface into these young leaves and, when they are
entirely matured and somewhat raised from the water, develop in them the characteristic pale
places which betray the presence of Doassansia in the leaves. It is also conceivable that Doas-
sansia conidia reach the mature leaves which are already above the surface of the water. It
is, however, not probable that they can penetrate into the already matured and hardened tissues
of the leaves. This penetration is limited rather to the meristematic tissues of the plant parts
which may be infected, as in all cases of smut fungi. These are the young and immature leaves
which in Sagittaria and Alisma are still submerged.
We may say that infection takes place here by means of water, since it is at least very
much limited outside the water in the mature tissues of the leaf and perhaps does not occur
at all. \\'e must not exceed here a brief mention of the noteworthy infection of host plants
of the Doassansiae le.st we anticipate the further results of investigation also for the forms
of smut fungi living in water-plants; for Ustilago longissima, which produces spore masses in
the leaves of Poa aquatica, and also for Ustilago grandis, which grows in brackish water on the
axis of Pragmitcs communis. It is probable that the infection of the germinating seedlings takes
place successfully in floating media and that the germs of infection distributed from the spore
masses through the water reach the young seedlings and attack them. The smut spores are
germinated in both cases with hemibasidia, which, according to their formation, were not as yet
(1) See Part XII of this work, plate XII.
42
definite in form and the conidia of which also grow out to new hemibasidia. These hemi-
basidia are propagated with the greatest ease in dirty water when organic substances for nutri-
tion are present in it, and they are brought here into natural association with the germinating
seedlings. Any kind of infection in these host plants other than the one indicated here is
scarcely to be assumed. Accordingly here in the infection forms of smut fungi there exist three
forms of dissemination, by wind, by insects and by water, just as has been proved for the pollen
of the blossoms of phanerogamic plants. It Ss noteworthy that three forms of infection so
important for the etiology of smut diseases have been entirely overlooked and therefore have
remained completely unknown.
43
INFECTION OF THE MAIZE PLANT.
It still remains necessary to subjoin the results of the investigations which were obtained
with maize smut and with the smut of Indian millet after the previous publication of Part
XI of this work.
So far as the etiology of the smut is concerned, the annual repetitions of infection have
given only a confirmation of the earlier results, the fact that all sufficiently young plant parts
are susceptible to the germs of infection from without and that the smut itself is strictly local-
ized on the infected places, is confirmed even by the interesting small result that the stigmaS
of the pistillate blossom spikes, if inoculated when young enough with conidia of maize smut,
can subsequently produce smut phenomena. The stigma assumes a garland-like appearance, bends
over the swollen pouch-like places and ripens into a small spore mass which forms perfectly
ripe smut spores. Such a stigma bundle, deformed by the smut-pockets, forms a highly inter-
esting picture worth noticing, a reproduction of which is not necessary here, since it may easily
be imagined. Of course older parts of the stigma are no longer capable of inoculation. One
can at most observe the penetration of the germ-threads of the conidia. An effect of infection
leading after 2-3 weeks to ripe spore masses can no longer be observed here. The most dif-
ferent varieties of maize were grown for further experimental infections, especially the large
form of the horse-tooth maize. In this the infections were less easily successful because it was
harder to reach from the outside the sufficiently young tissue, which is tightly inclosed by leaves,
meeting together over the vegetative point, and because under the same condition the young
pistillate blossom spikes are more tightly closed from the outside by the overlapping of the envel-
oping leaves, than is the case in the smaller forms of maize. If the opening from above to the
pistillate spikes is widened and the fluid for infection with its conidia is introduced, no differ-
ences may be seen from the smaller varieties of maize. The same phenomena of smut already
described occur here also. Experiments were further carried out, to show that an infection of
the young germinating seedlings is one of the greatest rarities. All sufficiently young parts
of the matured plant are attacked if they are accessible from the outside for the germs of
infection.
\Ve are concerned now only with showing how this infection takes place of itself in
nature. As already stated, it does not proceed directly from the smut spores. These smut
spores, which are not capable of germination in water, but may do so at any time in nutrient
solutions, produce conidial buds on saprophytic substrata, that is, in humus soil, and especially
in well manured earth. These conidia very soon pass over to the formation of air conidia1,
which are distributed through the air and are blown on to the maize plants, developing the
smut disease.
(1) Compare with these the Illustrations of the yeast-like conidia and the air conidia, as well as
the forms of their gro\yth, on plate IV, Part V.
44
The earlier experiments have not yet brought out the experimental proof that infection
of the host plants is truly brought about by saprophytic centres of infection of maize smut spores
which are deposited at a distance from the parts of the maize to be infected. The experiments
in this line have been carried out since and have been added to by annual repetition. On lots of
young maize plants which had already pushed 3-5cm out from the sheath, which therefore, as
young germinating seedlings, had become completely immune, smut spores were sown in such a
way, that, mixed with good humus soil, they were carefully sifted between the experimental
plants. Then a thin layer of horse manure was put on top and the surface stirred a long time
with a suitable rake until the manure was equally mixed with the soil. In this condition, all
the lots were left to themselves and further observed. It was shown in all cases where the soil
had been sufficiently infected and the content of dampness had been artificially regulated by rain
or by sprinkling at short intervals, that even after a few weeks the appearance of smut occurred
in the plants and later increased noticeably. All the phenomena of smut reappeared just as they
have already been described, in the leaves, in the staminate blossoms, in the axes, in the adven-
titious roots and subsequently also in the pistillate flower spikes1. The places of infection were
now arranged as described above, and separated one pace from each other, at varying distances
from the lots of maize plants so that the air conidia formed on the soil had to be carried farther
to the maize plants by wind from the prevailing direction. It was shown that even here infec-
tion takes place by means of air conidia, but that it decreases gradually with the increasing dis-
tance of the centre of infection from the experimental maize plants. Restricted by the given
special conditions the experiments could not be carried out at a greater distance than 20 metres.
It was possible to affirm, however, in each case that a number of maize plants had been reached
by the germs of infection carried by the wind and had become smutted. The easy dissemina-
tion of the very small air conidia through the air places no limit of infection in nature. Beyond
a certain distance, the results become reduced and only isolated instances of disease occur.
Certainly the universal distribution of -maize smut is chiefly promoted by air conidia, if not
entirely by them. If this be true, the overcoming of this smut can be attained only by burning
the smutted plants before they have allowed their smut spores to reach the soil; for its infection
proceeds always from the soil and the spores dropped from smutted plants on to it are later the
natural centres of infection for the increase of the disease.
Further, the experiment was not overlooked of collecting and sowing the still healthy
grains of maize spikes, which had been attacked by this smut only in the uppermost parts. It
was shown, as might have been presupposed, that this grain, sterilized before sowing, brought
forth perfectly healthy plants and that in the interior of the grains no vegetative fungus was
present. Of course the smut can be carried over in the seed of maize taken from smutted fields,
by the spores which cling to the outer surface. These spores get into the soil and, if it is
impossible for them to attack the young maize plants they may still become centres of infec-
tion which can bring about a renewed infection from the soil by saprophytic nutrition and by
(1) See plates III-V, Part XI.
45
the development of air conidia. On this account it is advisable to sterilize impure seed of
maize in order to destroy thereby all smut spores clinging to its surface.
If we take into consideration the fact that air conidia of the maize smut lead to infec-
tion of tin- mature host plant and that they alone may bring it about, that these air conidia,
driven by the wind into the openings and rifts of the host plants, attack the young tissues to
be found there and make them smutted, it then becomes self-evident that maize plants which, by
enveloping leaves, shut off all young tissues, susceptible to attack externally, must be at the same
time the most resistant to this smut. These are the large varieties, to which belong especially
the hor^e-tooth maize. It must be just as self-evident that the usually smaller varieties of maize,
in which the leaves open over the vegetative point like a paper sack and in which the pistillate
flower spikes are less protected by their husk leaves, show a marked susceptibility to the smut.
The experiments described above and reported in Part XI of this work1, were made accident-
ally with a smaller variety of maize which is especially suitable for experimental infection. Only
later comparative experiments with other maize varieties showed clearly how these are protected
by the above named accessory conditions from the blowing in of the germs of infection and
how it must naturally appear that in this variety the smut is formed only rarely.
(1) Plates III-V.
INFECTION OF INDIAN MILLET.
In passing over now to the smut of Indian millet, to Ustilago sorghi (cruenta), we have
a different form of disease in host plants, which forms spore masses exclusively and only in
the inflorescences. Infection most undoubtedly takes place here generally in the germinating
seedlings of fresh seed, even when the spore masses appear first in the flower panicles of the
mature plants. In earlier experiments, when infections were carried out in sufficiently young
germinating seedlings, as high as 70% of smutted plants was obtained. In later experiments
these results were repeated in approximately the same way1. However, it was assumed earlier
that infected plants could not develop spore masses if they outgrew the smut germs by too rapid
development so that these could not reach the vegetative tips. However, in all cases it could be
proved that infection had taken place in those plants by the fact that fungus mycelia were
shown in the nodes of the grass and in the parenchyma cells and that it had been retarded and
had not reached the vegetative point nor passed over to the formation of spore masses2.
In order to prove that infection had actually taken place, these plants were cut back to
two thirds of the height of the axis, as soon as it was seen that the panicle of the tip was
healthy. By this means the formation of axilla ry sprouts was caused and this formation takes
place, as described earlier in Part XI, at those points in which mycelia exist enclosed in the
parenchyma cells of the nodes. By this new formation of tissue for the axillary sprouts, paren-
chyma cells were affected which harbored the mycelia. These can here penetrate through the
young tissue and reach the vegetative points. It is now seen that in accord with the experi-
ments carried out previously with other plants, these axillary sprouts became smutted. There-
fore smut can be brought to development in apparently healthy plants as if by a stroke of magic,
if the apical healthy inflorescence is removed early enough, thereby causing the possibility of
an axillary sprout formation. In our climate this occurs very rarely in sorghum plants when
not artificially introduced. It can, however, take place, and with the result that the smut infec-
tion already existing will be subsequently proved by the smutted axillary sprouts. However,
these earlier experiments are capable of being multiplied from still another point of view. If
it is true that smut germs, which have already pressed their way in, are frustrated by too
rapid growth of the host plants and that thereby the decrease in the percentage of smutted
plants is brought about, the question arises whether this too rapid development of the host plant
cannot be restricted. This is most easily possible if seed older than that of the previous year
is used, the grains of which have weakened more or less in germinating energy with increasing
age. The young germinating embryos, whose development is retarded by delayed germination, are
most excellent material for further experimental infection of the young germinating seedlings.
This inoculation was carried on by means of an atomizer by the spraying with spores which had
stood a day in nutrient solution and which thus were brought to direct germination. It was
(1) Compare the text of Part XI, pages 43-51.
(2) Compare fig. 1, plate I, Part XI.
47
proved in the autumn that a total infection of the host plants had taken place here1. Unfor-
tunately such a totally infected field of Indian millet cannot be photographed, because the
-minted plants of these experiments are not conspicuous enough to appear as smutted ones in a
photograph. Imagination suffices to form a clear picture of this most striking phenomenon.
Further, the question is still unanswered whether in the smut of Indian millet infection
of the blossoms cannot also occur. Inflorescences are found which are totally infected. These are
usually the first to appear. Then follow other inflorescences which show only partial infection
and in which, between the smutted blossoms, may be found others blooming normally and pro-
vided with stamens and ovules. The sorghum sm ut is not as dusty as the loose smut, but it can be
blown with ease into the partially attacked inflorescences, or those perfectly healthy. Unfortunately
these experiments had no decisive results, because Indian millet in our climate ripens in separate
heads only in especially favorable vegetative years and forms ripe grain only rarely. Therefore
it can not be decided with certainty how far infection of the blossoms takes place here. In only
one case could healthy grains be gathered from partially smutted panicles in which a spraying
with the smut spores had been made use of. From these grains, however, healthy plants were
grown.
(1) The total infection obtained here gave ground for carrying out the experiments In the same
way for wheat and barley with seed of different ages. AM may be seen from the survey of Infection
experiments given In detail pages 26-30; the experiments, however, were unsuccessful.
INFECTION OF PANICUM (RISPENHIRSE) AND ITALIAN MILLET.
Besides the two plants experimented upon, maize and Indian millet, with the corre-
sponding forms of smut, during the last ten years two other experimental objects were grown
supplementally which are especially well suited for the purpose of infection. They are first
Panicum with Ustilago Panici miliacci (U. dcstruens), and then Italian millet with Ustilago
Crameri (U. Setariac). (
In Panicum the occurrence of smut is especially characteristic in its external appearance.
In the plants attacked, the otherwise loose, long, panicle-like inflorescence is shortened as much as
possible and all the single attacked blossoms united in a smut gall, which is enclosed by sheath
leaves. These leaves have undergone a complete fungus pseudomorphosis from mycelial threads
which have remained sterile and form a dazzling white envelope about the thick clump of
spore masses. The smut galls are sunken within the unchanged green leaves of the upper axis
and are only a very little exposed to the open air. The plants attacked, in contrast to a healthy
one with its long, outstretched blossom-panicle, make an entirely different impression, so that
they may be recognized in the field even from a great distance. The black spore masses
in the interior of the gall are not disseminated. They are, however, easily germinated in nutrient
solution or in water and produce four-celled hemibasidia, in which a formation of conidia
occurs, sometimes to a lesser, sometimes to a greater amount1. The conidia very rapidly
grow out to germ tubes and form in dilute nutrient solutions small mycelia, on the threads of
which may be observed the formation of air conidia. Further particulars are to be found dis-
cussed in detail in Part V of this work.
The ripened smut spores, sieved and well-preserved throughout the winter, are purified on
a centrifugal sieve and result, after twenty-four hours' retention in dilute nutrient solution and
also in water, in a directly aggressive material for infection. One can follow the rapidity with
which the spores germinate and form hemibasidia with conidia, which in turn grow out to germ
tubes. Inoculation was undertaken on previously chosen grains of Panicum, in which germi-
nation had just started, by means of the atomizer and the cultures, protected from the light,
were set back in a moderately warm place. After the lapse of a few weeks, the cultures were
opened, at first still protected, in order that they might be planted. In infected plants in a series
of experiments extending over several years, an average of 60-70% of smutted plants was har-
vested. The result in healthy plants could be explained easily by the fact that the compara-
tively small germinating seedlings of Panicum offer only a limited surface for the spraying on
of the germs of infection. However, the discoveries obtained previously with Indian millet
were established here also, in obtaining a percentage of smutted plants by delayed development
of the host plants, that is, of the young germinating seedlings. Seed from former years was
used for the experiments and it was determined with certainty that a slower germination took
place here, in which infection was carried out by means of the atomizer in the way described.
(1) See illustrations on plate VII, Part V.
49
Varieties of millet with black grains and with white ones were used. The result, which con-
tinued to be the same in succeeding years, was the most favorable conceivable, namely, a total
infection of all the plants under experimentation. The variety of millet with white grains is best
suited to give striking and beautiful illustrations of smut phenomena. The plants obtained a
height of more than 4 feet and the galls of smutted ones became a large as a walnut.
An experimental object more favorable for the inoculation of young seed than that exist-
ing hero in millet is scarcely conceivable. It is still undecided, however, whether infection takes
place only on the young germinating seedling or whether it can also take place successfully
in the blossoms. The proof of air conidia in this form favors the infection of the blossoms
of the host plant. The single blossoms of these host plants are, however, so small that the prob-
ability of blossom infection is thereby greatly reduced. It should be added to this that the smut
galls in experimental fields are not disseminated and therefore could not succeed in reaching
the soil directly, so that any direct formation of air conidia is thereby practically prevented.
Infection must then have taken place from the conidia of a saprophytic nutrition. They can
be formed on the upper surface of the soil from spores which had been previously dissem-
inated. The probability that this may happen is not great. Still greater, however, is the
other probability that in sowing millet in the open air the young germinating seedlings are
reached by air conidia. Practical experiments on the inoculation of the blossoms resulted nega-
tively. Infection of the blossoms is, however, in no way excluded by this, but is reduced to a
minimum.
Experiments with Setaria Italica with its smut forms had about the same results as those
described above for Panicum. A black shimmer may be seen in this thick, club-like inflores-
cence, already infected, when the ripe ovules rupture, freeing the smut. The black smut spores
are not disseminated. They usually remain so enclosed in the thick panicle of Italian millet
that close examination is necessary in order to recognize plants attacked by smut. It often
occurs here that only a part of the blossoms of a panicle are attacked and that normal blossoms
free from smut may be found between the diseased ones. The smut spores in any case germi-
nate into four-celled hemibasidia, in which often no conidia at all occur, which, if they do
appear, however, grow out very quickly into germinating tubes. Air conidia have not been
observed in cultures of these spores. Smut spores, obtained pure in the autumn, germinated in
the spring, easily and surely, especially in dilute nutrient solutions. They were used further
only after purification with a centrifugal sieve and after one day's retention in dilute nutrient
solution. They were sprayed on the seedlings of Setaria which had been thus prepared and
were just germinating. The cultures were treated as above and the infected seedlings, when
they had reached a sufficient size, were planted out of doors. These seedlings are exceedingly
small, so that one might suppose inoculation by spraying with spores would have no result in
the experimental plants. Experience, however, proves the opposite ; as high as 70% of smutted
plants were obtained and it was possible to achieve here, as in Indian millet, and Panicum, a total
infection, by using for this infection seed which is somewhat older and therefore sprouts more
slowly.
So
With the absence of easily disseminated spores and also lack of air conidia, blossom
infection is here from the very beginning improbable. This could be promoted only by the special
circumstance, that in partial infection of a flower spike, healthy blossoms may occur between the
smutted ones and therefore be directly adjacent to these. The possibility thus given for blossom
infection could be easily tested by harvesting the ripe seed from partially smutted spikes and
using it for sowing the following spring. The results of these experiments gave no smutted
plants. Accordingly, the probability of infection in the blossoms in any case is very slight, if
it exists at all.
In the experimental plants last treated, that is, Indian millet, Panicum and Italian millet,
we have varieties and host plants for smut fungi in which the infection of the germinating seed-
lings may be considered as the prevailing type of infection in smutted plants, if not the only
one, while the infection of the blossoms, if it takes place here at all, seems to be limited to a
small amount.
Spraying with the germs of infection by means of an atomizer was especially suitable
for carrying out the infection of the young germinating seedlings, if the precaution was taken
of purifying the spores with a centrifugal sieve and of preparing them for direct germination
by one day's retention in dilute nutrient solution.
Further plants for experiment have not been taken up as yet in our investigations and
experimental infection. The exceedingly important smut forms of the stinking smut of wheat
and the covered smut of barley have not been overlooked, but at first only several experiments
could be arranged, because it was impossible to undertake and observe too many experiments at
one time and because it was better to await the results of those already undertaken in order
to use them explanatorily when making others.
Blossom infection with stinking smut of wheat and the covered smut of barley were begun
last summer, however, and will furnish results only in succeeding vegetation periods.
FINAL CONSIDERATION.
From the preceding experiments as a whole, it is obvious that the previous assumption
of a successful infection of smut fungi limited only to germinating seedlings is not universally
satisfactory. Besides infection of the young seedlings still other forms of infection exist which
had been overlooked.
We can report in general that only the youngest embryonic tissues of the host plants are
the ones attacked by the germs of infection. The germs of the smut fungi have no power of
attacking older parts of plants the tissues of which have become hardened.
Experiments on the infection of maize smut proved clearly that the large host plants, in
the case of their development and formation, expose in different places the youngest embryonic
tissue to the attack of infection germs of maize smut. These points of attack extend even to
the embryonic pistillate inflorescences which usually appear only after the complete maturing of
the plants. In maize the young leaves of the vegetative tip, the staminate inflorescences and the
young axes may be reached by germs of infection, blown upon them. In the same way also
infection of the pistillate inflorescences and adventitious roots takes place in the host plants.
That infection has taken place is easily and surely determined here and the appearance of smut
occurs after the lapse of perhaps three weeks. The smut remains locaffzed upon the separate
places in which inoculation was successful and occurs independently on all the above-named
places which are susceptible to smut germs and capable of infection by them.
In the other smut forms occurring in our grain the matter is essentially different. The
phenomena of disease do not develop in the parts in which infection has taken place. The
effect of the infection is shown only after a long period of incubation, after many months, with
the unfolding of the inflorescences. In the inflorescences alone are provided the only places for
the formation of spore masses and these inflorescences lie at the opposite end of the host plant
from the one attacked in the first stages of the germination by the germs of the fungi. The
host plants during their whole life are surrounded externally by mature and hardened tissues,
into which the germs are not able to penetrate. The host plants only once and indeed only at
the beginning of their development offer external young tissue to the germs of infection. These
are the first germinating stages of the young seed in which infection must take place in the soil,
if smutted plants are to be produced subsequently. These facts correspond throughout to the
previous and older theory that infection of smut fungi takes place in the young seed. This
undoubtedly happens, but in thus judging it, the fact was overlooked that host plants, at the time
of flowering, offer again in their ovules and stigma? very young and assailable tissue for the
germs of infection and that infection can take place in the embryonic parts of the pistillate inflor-
escences as well as in the young germinating seedlings in the soil.
Thus our investigations have produced certain proof, that this infection actually takes
place in the blossoms and that, carried by wind or insects, the smut dust is brought from smut-
ted individuals to healthy plants.
52
This very obvious example of infection in the blossoms had been hidden and kept from
a full understanding by the fact that the smut in the infected blossoms did not appear in the same
year with the ripening of the grain; that rather the germs of infection which hai'c penetrated into
the seed lie latent there and develop in the matured and blossoming plants only in the following
year, with the germination of the seed. Blossom infection, however, which could be proved
with certainty in the pistillate spikes of maize occurred here therefore in a varied form, in that
the period of incubation up to the breaking out of the disease, that is, until the spore masses
mature, is considerably longer. It is not spanned by three weeks, but is completed only in the
second year, following the finished inoculation. In this noteworthy fact lies the peculiarity of the
now ascertained blossom infection of our varieties of grain.
Accordingly, in the occurrence of smut diseases in our grains, we must reckon with two
places of infection quite independent of each other; first, the young germinating seedlings,
second, the blossoms. We must consider that in separate cases both forms of infection may
be effective at the same time, but first one and then the other will be predominantly active. In
judging of the natural spread of smut fungi and smut diseases, these recently explained facts are
of decided value.
However, in the details here given only the development of the parasites within their host
plants has been considered, the different forms in which infection takes place and also how,
from the germs of infection already present, the further development of the smut fungi and
of the phenomena of diseases is carried up to the formation of spore masses.
Now, however, by means of the earlier investigations and cultures reported in Parts V,
XI and XII of this work, it has been proved that smut fungi can live not only in the host
plants, but that they occur also outside of the host plants on saprophytic substrata and mature
there in different and new forms, which have not been observed within the host plants. How-
ever well smut fungi, as parasites in the host plants, may show the most complete adjustment
to their hosts, which adjustment can be observed only in nature, they are rather not specific
parasites, but only facultative ones. They may live and flourish outside the host plants in all
substrata to be found in nature. A rapid and active development of the smut fungi takes place
in these nutrient substrata and especially an exceedingly abundant increase of the germs. Smut
fungi live in nature outside the host plants just exactly as do other saprophytic fungi and their
propagation takes place especially where nutrient substrata are present in humus and well
manured soils. A saprophytic development results here and also a propagation of the germs.
From these places, as in maize smut where air conidia are formed, the germs of infection can
be distributed on to the susceptible parts of neighboring host plants. In other cases where air
conidia are absent, the germs of the smut fungi, developed and increased in the soil, will attack
the young germinating seedlings and produce the phenomena of smut.
Further, nutrient substrata, independent of soil, for the development of smut fungi, may
be found in the secretion of the stigmae and in the honey of plants fertilized by insects. In all
such cases saprophytic nutrition of the smut germs introduced in these places may be proved
with certainty.
53
According to the earlier hypotheses, infection was dependent on the direct products of
germination of the smut spores: therefore, solo speak, on these alone. It was assumed from
llii- -weakly germinating smut scores that they inoculated the germinating seedlings and that
from these inoculations smutted plants were produced in our grain fields. This theory, however
short and convenient for the explanation of smut infection, has been supplemented by the proof
of an extensive distribution and propagation of the smut germs in saprophytic substrata outside
of the host plants. Only by determining this has the KWV. I'M which the germs of infection are
distributed, become clearly and certainly understood, as well as the natural infection and distri-
bution of smut germs as observed universally in nature. The biological section with the devel-
opment of smut fungi on saprophytic substrata outside the host plants, forms, according to our
present understanding, the complement of the section with development taking place in the host
plants. Both parts are now united in a harmonious whole and nothing can characterize this
harmonious union further and more sharply than the fact that, for instance, in the forms of\
the genus Ustilago. at the time of parasitic life in the host plants, only chlamydospore fruit forms,
tlie typical smut spores, mature and that during the period of saprophytic nutrition only conidia
fruit forms appear. For this strict alternation in the maturing of the fruit forms which takes
place here, not, as in the case of the Uredineae, on two different hosts, but after saprophytic and
parasitic nutrition. TIT can for the present find no other explanation than the influence exer-
cised on the development of our plants, at one time by the living substrata, the next time
by the dead substrata. How would it be possible, according to the earlier conceptions and the
earlier knowledge which had not led even so far as to the germination of the smut spores, to
explain the phenomena in maize smut and to understand them correctly, if the portion of the
development of smut fungi enacted saprophytically did not furnish the natural explanation for
all details? It is scarcely possible to find anywhere in the whole domain of infectious diseases
a more complete or finer picture of this most striking phenomenon as it exists most clearly here
in the etiology of the maize smut. And not less clear has become the understanding of the
>mut forms living in our grains which propagate their germs of infection in the soil by sapro-
phytic nutrition and especially in manured soil, in such a way that infection* of the germinating
seedling may thereby be understood and the significance of manure for the occurrence of smut
diseases in grain as agriculturists have always emphasized is shown in the proper light.
i i rtainly, however, the phenomena of blossom infection are not less convincing and clear.
In them the smut germs find their nutrient substrata in the secretion of the stigma and the
exudation of honey, which are as favorable as pqssible for germination, development and propa-
gation of the germs of infection.
It took a long time, more than the lapse of twenty years, to make possible the obtaining
of the explanations here given concerning the biology of the smut fungi, their infection, the
phenomena of the disease and the natural distribution of smut fungi on saprophytic substrata.
It was not easy to find in the separate cases the right road which would lead to this goal.
It should be noticed here, however, that ,the universal end of the new investigations, how-
ever successful they have proved to be in the cases already carried on, has not in any way been
reached and that still many separate experiments must be carried out in order to obtain the
54
results made possible by this newly acquired understanding of the matter. The investigations are
therefore as difficult as they are wearisome and experimental infection encounters impediments
in the undertaking and in its carrying out which are scarcely imaginable in advance.
The peculiarity of these experiments on infectious diseases in plants is that they can be
carried out in part only with the resources of an institution ; and in part, moreover, only with
those of an experimental field in which the cultures of inoculated plants must be brought to a
finish. The undisturbed harmonious co-operation of these two factors, the arranging of the
experimental field, the preparation and the work in the institution, is possible only if the experi-
mental field and the work rooms of the institute are as closely and conveniently connected as pos-
sible. Only thus is it possible to observe the cultures for any length of time and to keep away
the many kinds of external disturbances to which they are exposed in the course of the period
of growth.
The chief impediment to the rapid progress of investigations and experiments in this
direction lies, however, in the circumstance that, during the whole length of time of one growing
period, experiments can be made only once, the results of which are given only at the end of the
summer. If these experiments have been disturbed by secondary and other injuries, or if they
give only negative results, a whole year is lost be fore the experiments can be renewed and supple-
mented. Thus several periods of growth are often needed for the deciding of simple questions
and the end of the experiments can be reached only years later, by the dispatching of questions,
possible only from time to time. In this way it becomes obvious that the investigations reported
here have not been absolute, even in the most favorable cases, but are only relatively conclusive.
In many places, the points in question have been left open where the results already obtained
from the cultures have not been sufficiently decisive. Years must still elapse before one can
speak of universally conclusive results.
If one considers this state of affairs and the unusual circumstances which come into con-
sideration in the experiments and their carrying out, one will involuntarily be led to think that
an arrangement suitable for the investigation of smut diseases and similar infectious diseases
would be most opportune. If only the damages which are annually caused by the smut of grain
be compared with the expenses of an institution of the kind indicated, this small material sacrifice
would certainly not be proportionate to the prospective advantages of an explanation of the
natural spread of smut diseases and the successful struggle against them. But here the external
resources of an institution and of the experimental field are not primarily concerned. Even if
these are granted no favorable results can be obtained when there does not lie at the disposal of
the management of such an institution a power broadly educated in the understanding of the
matter and also mycologically.
55
OF THE ASSIMILATION OF NITROGEN'.
In the inoculation of blossoms with the loose smut of barley and of wheat it has been
proved |M>~M!>IC to harvest grain which after sowing gave total infection of all plants under
experimentation. In the same way in the smut of Indian millet, Panicum and Italian millet, a
total infection of the plants under experimentation was obtained, if the germinating seedlings
were inoculated sufficiently carefully by means of an atomizer. We have accordingly in the
host plants of the smut fungi here named material which will lead with perfect certainty to the
formation of smutted plants.
With this material it has now been possible to decide definitely a physiological question
of especial interest; namely, the question as to a possible assimilation of free nitrogen by the
fungus mycelia which live parasiticaljy in their host plants. This question became of importance
through the excellent investigations of Hcllricyel, which prove definitely that lupines and other
Leguminoseae can live in soil without combined nitrogen, that is, chemical compounds of nitro-
gen, and are able to assimilate the free nitrogen of the atmosphere, if they are inhabited by para-
sitic fungi. Hcllricyd succeeded in bringing the above-named Leguminoseae to full development
in pure vitreous sand, which had been provided with mineral salts in solution, but remained free
from combined nitrogen, if definite forms of bacteria rhizobia could attack the roots of these
host plants and produce tuber-like swellings there.
The fortunate results of HdlricgcFs cultures have brought forward the question whether
other fungi living parasitically in their host plants can cause a similar assimilation of free nitro-
gen. A series of phenomena, for instance, mycorhiza, which occur universally distributed* on
the roots of different plants, favors its explanation in this way. Experiments were made with
tree-like plants several years old, in which it was thought possible to prove that the mycorhiza
living on the roots can cause assimilation of free nitrogen. Experimental material in perennial,
slowly growing plants, said to assimilate uncombined nitrogen, does not promote, however, the
decision of this question as to the assimilation of free nitrogen. In time, unavoidable sources
of error creep into experiments with perennial plants, which offer no security for a scientifi-
cally certain result. Experiments of this kind can be carried through successfully only with
quickly growing and large annual plants through which the proper parasitic fungi grow, from
germination to the end of development, and which attain the most luxuriant development pos-
sible. In this kind of experimental object, it must be assumed that parasites of these plants
living saprophytically do not cause the least damage and that some connection exists between
the parasites and the host plants, as was found in the Leguminoseae and their rhizobia. Experi-
mental objects of the necessary and desired kind are furnished now in an absolutely ideal form
in our large annual grain species which smut fungi attack- and in which they live. In one
vegetation period a plant attains its complete size and maturity. The parasite penetrates into
(1) A preliminary report on this subject has been published In a lecture before the Schlei. Gesell-
•chaft fUr vaterlandlsche Cultur, on the 15th of November. 1800.
56
the plant in the first embryonic points, continuing its growth with the maturing of these, until
at the end of development they pass over in the blossoms to the formation of spore masses.
The adjustment of the parasite to the host plant is the most complete possible. Nothing at
all of any appearance of disease is to be seen in the course of the whole development of the
host plant up to its complete maturity. In fact the phenomena are constantly repeated, that
the host plants attacked by fungi develop more quickly and luxuriantly than healthy ones and
that spore masses have appeared in them when the inflorescences are just beginning to show
in healthy plants. One is tempted involuntarily to believe that parasites living in infested
host plants can exercise an influence favorable for a quick and complete development. These
external circumstances make somewhat desirable the choice of these experimental plants as objects
for the decision of the question whether fungus threads living parasitically in their host plants,
here especially smut fungi, are able in connection with these to assimilate free nitrogen and
thereby be in a position to cause a more luxuriant nutrition of the host plant.
Up to this point only one impediment had been found in using host plants attacked by
fungi for this kind of experimentation and this lay in the circumstance that in the experiments
it was never certain whether the plant under experiment had been attacked by smut and whether
one was actualy working with smutted experimental objects which alone could bring about a
decision of the question. This impediment has now been overcome by the continually improved
methods of inoculation of host plants with smut fungi. It became possible in the different millet
forms, — Indian millet, Panicum and Italian millet, — to produce with certainty infected germi-
nating seedlings for the experiments and just as surely to use seed obtained from blossom infec-
tion which from experience was seen to produce only smutted plants.
The natural method of arranging the details of the experimentation works out of itself, —
as Hcllriegcl had planned it. According to him, sterilized absolutely pure vitreous sand was
saturated with mineral nutrient solutions, but without any nitrogen compounds, and then put
in glass jars, which, sunken in soil, were provided with openings and a covering of gravel for
purposes of ventilation. In this substratum the freshly infected germinating seedlings of the
three millet forms, — Indian millet, Panicum and Italian millet, — were planted in separate pots,
from 3-5 specimens being put in each. The single plants were weighed on the decimal scales
at the beginning of the experiments and daily loss through evaporation was replaced with dis-
tilled water free from nitrogen. For comparison, pots were arranged in the same way as those
described above, only with a corresponding addition of a nitrogen compound in the form of
calcium nitrate. In these parallel experiments the same number of experimental plants, that is,
germinating seedlings, were planted in each pot. The experimental plants were then placed under
protection in the propagating house and in good weather carried into the open air on a truck in
order to expose them to the direct sun. Thus, with this method of setting up the experiments,
sources of error could not creep in. The transplanted seedlings in both series of experiments
grew without climculty in the vitreous sand and in the first eight days showed scarcely noticeable
differences. Then after the exhaustion of foodstuffs in the germinating seed, the lack of nitrogen
on the one hand and the action of the nitrogen compound on the other, first made themselves felt
and led to an even more striking phenomenon. In the next four weeks the pots without nitrogen
57
compounds showed scarcely any advance in the young plants, while the plants in the pots with
nitrogen compounds matured daily more luxuriantly. After six weeks the contrast was as great
as possible. When no further advance in the development of the dwarfed plants without nitrogen
compounds could be observed, a correspondingly slight amount of nitrogen compounds was intro-
duced in the sand in the solution. Even in the next few days the effect was apparent. The little
plants developed further and. after the lapse of about three months, so far as their size, even if
dwarfed, permitted, the formation of blossoms could be recognized. When these had matured it
was shown that all experimental plants had become smutted, as might have been presupposed.
Also in the comparative series of experiments abundantly provided with nitrogen and in which
nitrogen compounds had also been added subsequently in order to cause the greatest possible
development, the plants did not remain in size much behind those in the open field and showed
in the inflorescence development of all individuals the most luxuriant formation of smut. By
means of photographic exposures (made by R. Scholz) the two parallel experiments of the
Sugar millet (Zuckerhirse) have been permanent and are reproduced in fig. i, plate 2, of this
volume.
The result of the comparative experiments shows most conclusively that fungus threads
living parasitically, in this especial case, of smut fungi, are not able to bring about the provision
of their host plants with nitrogen from the air. Without nitrogen compounds, they soon stop
growth and resume the phenomenon only when further nitrogen compounds have been added.
From a comparison of the dwarfed plants without nitrogen compounds with the luxuriant normal
forms obtained by means of them, it is seen conclusively that filiform fungi, living parasitically
and concerned here, are not in a position to bring about an assimilation of free nitrogen even when
the most favorable objects are grown for the experiments. If assimilation of nitrogen cannot be
proven here, there is no great possibility that it can be the case in other fungi living para-
sitically. The somewhat quicker and more luxuriant development of host plants attacked by
fungi, mentioned above, must have other subsidiary causes which, however, in any case may not
be traced back to nitrogen assimilation.
Experiments with these millet varieties were repeated in the course of three years and
always with similar results. Wheat and barley were used only later for the same experiments.
Instead of young inoculated host plants, the experimental pots were sown with grain which
had been kept over from previous harvests, in which there had been a total infection of the
harvested grains. The experiments were set up and carried through in the same way as those
described above. During the period of experiment no disturbances whatever occurred and the
results were exactly the same as described for millet. The grain germinated into healthy seedlings,
which, lacking nitrogen compounds, stopped growing after all the reserve stuffs had been used
up. When in the course of three or four weeks this cessation of growth took place, the plants
were so benefited by a single addition of nitrogen compounds that they formed small inflor-
escences, which in every case were entirely Minuted. The comparative experiments with nitro-
gen compounds again gave a normal development of the plants and also the formation of com-
pletely matured smutted heads. By photographic exposures the actual condition was made
58
permanent and visible here as in millet. The series of experiments with infected barley and with
wheat substantiated in short the earlier results with millet. In this can be recognized no proof
that any assimilation of free nitrogen takes place, caused by parasites in the host plants, and we
can say directly that the host plant infected with smut is here exactly as dependent on nitrogen
compounds as are other healthy plants. The negative result of these experiments makes the facts
ascertained by Hellriegcl, for Leguminoseae, appear so much the more prominently. The subject
is finally limited to the fact that according to our present knowledge only the rhizobia possess
the capacity of bringing about assimilation of free nitrogen to any great amount when living
parasitically on the roots of Leguminoseae.
59
EXPLANATIONS OF THE ILLUSTRATIONS.
PLATE I.
Fit;, i. A small totally smutted experimental field of summer barley, grown from sterilized seed,
which, as blossoms, had been inoculated with fresh smut s|H>res. Many heads have
become only partially smutted.
Fig. j. A similar experimental field of summer wheat. The few healthy heads belong, however,
to smutted stalks.
In the text this fig. 2, as a result of an inadvertent reversal of the pictures, has been
designated as fig. I.
PLATE II.
Fig. i. Smutted experimental plants of the Sugar millet, which were inoculated as young ger-
minating seedlings. The pot at the left contained all kinds of nutrient salts, including
calcium nitrate, the one at the right, no combined nitrogen. In the latter the experimental
plants, after the addition of calcium nitrate solution, developed and formed blossoms, all
of which were smutted.
Fig. 2. Smutted experimental plants from sterilized two-year old wheat grain which two years
previously were inoculated with smut spores at the time of flowering. The right hand
pot shows the development of smutted individuals in pure vitreous sand containing all kinds
of nutrient salts, including calcium nitrate. In the left hand pot development took
place at first without the addition of combined nitrogen. Later, however, a slight amount
of calcium nitrate was added in order to further the development up to the formation of
blossoms. In this part also all individuals were smutted.
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