CONTENTS
Introduction
ix
Major Groupings of Imperfect Fungi and Their Importance
in the Biosphere
x
Cytological and Morphological Features of Imperfect Fungi
xvi
Factors Affecting Growth and Sporulation of Imperfect Fungi
xviii
References Cited
xxi
PART I. PHYSIOLOGY
ISOLATION
CULTURE MEDIA
1
1
2
MAINTENANCE OF STOCK CULTURES
PHYSIOLOGY: NUTRITION AND ENVIRONMENT
2
3
USE OF IMPERFECT FUNGI TO ILLUSTRATE BIOLOGICAL PRINCIPLES
4
PART II. TAXONOMY AND IDENTIFICATION
6
THE SACCARDO SYSTEM OF CLASSIFICATION
FAMILIES OF MONILIALES
6
7
KEY TO GENERA
8
MUCORALES
MONILIALES
HELICOSPORES
NOT HELICOSPORES
MONILIACEAE
DEMATIACEAE
8
9
9
10
10
17
TUBERCULARIACEAE
STILBACEAE
25
26
SPHAEROPSIDALES
MELANCONIALES
MYCELIA STERILIA
28
33
34
SIMPLIFIED KEY TO SOME SELECTED COMMON GENERA
35
THE HUGHES-TUBAKI-BARRON SYSTEM OF CLASSIFICATION
40
vii
ALTERNATE KEY TO SERIES AND GENERA
ARTHROSPORAE
MERISTEM ARTHROSPORAE
ALEURIOSPORAE
ANNELLOSPORAE
BLASTOSPORAE
BOTRYOBLASTOSPORAE
POROSPORAE
SYMPODULOSPORAE
PHIALOSPORAE
*
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
41
44
44
45
48
48
5051
52
55
59
REFERENCES
198
GLOSSARY
212
INDEX TO GENERA
216
vill
INTRODUCTION
The Deuteromycetes or Fungi lmperfecti (former taxonomic designations) are an anomalous,
heterogeneous assemblage of asexual ascomycetes and basidiomycetes which no longer have formal
taxonomic status. These fungi were traditionally considered as lesser fungi because they lacked the
perfect stage—sexual reproduction. The absence of asci (ascomycetes) and basidia (basidiomycetes)
prevented their assignment to a natural taxon and necessitated .artificial non-sexual characteristics to
describe and classify them. This genetic inability of many imperfects to reproduce sexually is considered
a primitive condition and in contemporary mycology presents a taxonomic quandary. Alexopoulus et al,
1996, provide excellent scientific rationale for excluding imperfect fungi from contemporary fungal
systematics, and discuss considerations needed to develop logical and valid taxonomic approaches to
determine their phylogeny (1). Consequently, the taxons which previously were recognized as
taxonomically valid for the deuteromycetes (imperfect fungi), are used in this book only to facilitate their
identification.
The imperfects are important eucaryotic microorganisms (possessing nuclei and organelles) which
affect humans and most other life forms in a myriad of ways. The need to determine their identities is
paramount in research, industry, medicine, plant pathology and in many other disciplines. Imperfect fungi
are identified according to their conidial or non-sexual states. Nevertheless, many imperfects possess
sexual structures of known ascomycetes or basidiomycetes, whereas others produce no conidia and/or
sexual structures. Roper, 1966, described a parasexual cycle in which genetic recombination can occur in
hyphae (16). This observation suggests that some fungi may never have possessed sexual structures or
required sexual reproduction for genetic exchange. However, while there is little data which substantiates
that pansexuality occurs under natural conditions today, it could have occurred during the origin and
evolution of these fungi.
When sexual structures are associated with the conidial state, a valid taxonomic status can be ascribed.
However, this often does not occur, and for practical purposes is not important. Although the scientific
name of the sexual state constitutes a valid taxonomic designation, the imperfect name is retained for
practicality and for conventional use. Therefore, to identify the imperfect fungi, it is necessary to know
their conidial morphologies regardless of whether the sexual state is also present in culture or in nature.
The deuteromycetes constitute an important group of fungi which require continued study despite their
obscure and confounding systematic relationships both to themselves and to other fungi. Barron, 1968
(2), Hunter and Barnett, 1973 (10), Hunter « tf al., 1978 (11), and Alexopoulus et al. (1) provide additional
information on many aspects of the morphology, sporulation, growth, ecology and economic importance
of imperfect fungi.
Scanning electron and light photomicrographs are provided on several of the following pages. They
show conidia, conidiophores, and hyphal structures found on many different kinds of imperfect fungi.
Compare them with like illustrations in the book to better understand how these structures are important
in identifying imperfect fungi.
IX
MAJOR GROUPINGS
OF I M P E R F E C T FUNGI AND T H E I R
IMPORTANCE I N T H E B I O S P H E R E
The imperfect fungi or deuteromycetes have been classified according to principles established by
Saccardo in Sylloge fungorum (17). While this taxonomic system is no longer valid, it is still the best way
to learn the mycology that is necessary for identifying the imperfect fungi. It is also the primary means
used in this book to identify imperfect fungi. The scientific names of imperfect fungi are still used, albeit,
only in a non-taxonomic sense, and as a necessity to know their practical importance in the biosphere.
The Hughes-Tubaki-Barron System (conidial ontogeny) has also been used as a way of classifying and
identifying these fungi (2, 9, 18). Details pertaining to this system are provided on pages 40-44 and
related identification keys are found on pages 44-57. The use of conidial and conidiophore ontogeny for
identifying deuteromycetes should be used by individuals who are well versed in mycology. The shape,
pigmentation, and septation of conidia are important characteristics in the Saccardo System but reduced
to secondary importance in the Hughes-Tubaki-Barron System.
To better understand the Saccardo System, common and economically-important imperfect fungi of
the four form orders will be presented. Following the Saccardoan System, the species of the form orders
can be separated into four distinct groups of fungi. This provides a basis from which to begin a search
(appropriate key) for the identity of an unknown fungus. The form orders are as follows: (I) Moniliales Conidiophores and conidia occurring free and distributed over the mycelium. Conidiophores may be
separate, in clusters, or in tightly-packed groups. Illustrative examples and accompanying descriptions of
many of the diverse genera in this group are provided from pages 68 through 161; (2) Sphaeropsidales Conidiophores and conidia contained within asexual fruiting bodies called pycnidia. See pages 162
through 187 for descriptions and illustrations of pycnidia-producing fungi. (3) Melanconiales - Conidia
typically produced under natural conditions in an acervulus, an open saucer-shaped fruiting body. In
culture, conidiophores may be single or in compact groups similar to sporodochia of the Mormiaies.
These fungi can be found on pages 188 through 194; (4) Mycelia Sterilia - Species in this form order are
genetically incapable of producing conidia or any kind of reproductive cells. Sclerotia or other survival
structures occur in the mycelium. Descriptions and illustrations of the three species depicted in this book
are provided on pages 196 and 197.
Conidiophores ot Paecilomyces sp. with typical flaskshaped phialides and catenulate conidia.
Conidia of Trichoderma sp. emerging from apices ot the
conidiophores.
X
Two of the spomlating form orders, Moniliales and Sphaeropsidales can be separated into several
form families. Characteristics are predicated upon such artificial features as color, shape, and consistency
of the pycnidium in the Sphaeropsidales, or color of the conidia and presence of synnemata or
sporodochia in the Moniliales. The form family taxon is not used in Mycelia Sterilia and only one form
family exists in the Melanconiales.
There are at least 1,400 form genera of imperfect fungi and several thousand species. The most
common in nature and the most economically important are found in the form order Moniliales. Some are
pathogens of plants, animals and humans, some produce toxins, while others are important in the
production of antibiotics and other chemicals. In the Saccardo System, it is the color and morphology of
the conidia which are used to separate form genera into sections. For example, one-celled hyaline (devoid
of any color) conidia are called hyalospores; colored, one-celled conidia are phaeospores; didymospores
are two-celled; and transversely septate conidia with three or more cells are phragmospores. Add hyalo to
phragmospore (hyalophragmospore) and it is a hyaline, transversely septate conidium; cylindricallyspiraled, one to several cell formations are helicospores, regardless of the presence or absence of color.
Problems encountered when using the Saccardo system are variations in type of fruiting body (acervulus,
sporodochium, and pycnidium), conidium color and conidium morphology. These structures can vary on
different media and in their response to varying environmental conditions. Consequently, what is
described in the keys may differ slightly to significantly when the fungus in question is grown on
different media or when it is incubated at different temperatures. Nevertheless, time and experience will
negate these factors. Therefore, because of its simplicity and practicality, the Saccardo System is still the
best way for students and others to study and identify imperfect fungi.
SACCARDOAN FORM ORDERS
FORM ORDER MONILIALES
Most species of deuteromycetes reside in this form order and are grouped into four form families (see
page 7). This is the only form order in which form families are described in this book. Form families
Moniliaceae and Dematiaceae have species which are delimited by one or more of the following
Conidia In basipetal chains radiating from the apex of an
Aspergillus sp. conidiophore.
xi
characteristics: conidial septation; conidiophore appearance and branching; conidial morphology; true
and pseudomycelium (some imperfects are yeasts without true hyphae); the manner in which the conidia
are produced; presence of chlamydospores and morphology; conidia produced in chains or in a head;
presence or absence of mucilage; conidial number and arrangement at apex of the conidiophore; conidia
produced on conidiophore or mycelium; and exogenous or endogenous production of conidia. Refer to
page 68 through page 145 for numerous examples of the Moniliaceae and the Dematiaceae. Note that
imperfects in this form order with hyaline conidia are members of the Moniliaceae; those with pigmented
conidia and/or conidiophores reside in form family Dematiaceae. The reason that the fungi of these two
form families are discussed together is because the only difference between the species is the color of
their conidia and conidiophores. This seemingly obvious color difference is at times difficult to
determine in culture and under the microscope. However, careful use of the microscope, diligence and
experience in identifying these and other fungi, will in time allow orje to make accurate determinations of
pigmentation, along with many other pertinent fungal characteristics.
Many of the more common fungi are found in the form families Moniliaceae and Dematiaceae.
Species of Aspergillus (page 95), Penicillium (page 95), Alternaria (page 132) and Stemphylium (page
132) are routinely isolated from the air and numerous other substrates. These genera and several other
species of the Moniliaceae are discussed here. Aspergillus fumigatus is an opportunistic pathogen of
humans and other animals and is responsible for the human disease aspergillosis, a pulmonary disorder.
Penicillium chrysogenum and closely related species are the sources of penicillin, an important
antibacterial antibiotic, which has saved countless humans from death and serious illness for many
decades. Other species of Penicillium are responsible for the contamination of food and clothing.
Gl'tocladium spp. (page 93) are similar to the penicillia, but differ at maturity by having the spore mass
encompassed by mucilage. One species, G. roseum is a good example where identification is confusing
because it produces two different conidial types, one being the Gliocladium type and the other that of
Veriicillium albo-atrum (page 92). Fortunately, this is unusual, but warns one to not always consider
fungal cultures contaminated when two distinct conidial types occur in the same culture. Verticillium
albo-atrum is a destructive plant pathogen that causes a wilt of some economically-important plants.
Monilia (page 73) cinerea var. americana, the pathogen of brown rot of peach and other fruits, is often
found as a contaminant of microbial cultures. Geotrichum candidum (page 68) is the causative agent of
geotrichosis, a human disease which can occur orally, in the intestine and as a pulmonary disease.
Species of the genus Candida (page 71) are common in the Moniliaceae. Note that this fungus is not
always filamentous, but can possess yeast-like cells. An important species C. albicans, is an
opportunistic human pathogen causing oral and vaginal diseases and may become systemic. This
filamentous yeast can be differentiated from other Candida spp. by the production of S to 12 pm
spherical chlamydospores on corn meal agar.
One-celled Gliocladium sp. conidia in mucilaginous masses on penicillate branches of conidiophores.
xii
Many species having pigmented conidia and/or conidiophores, reside in the form family Dematiaceae.
Many of these species are also common and/or economically-important fungi. Stachybotrys (page 89), a
soilborne saprotroph, has pigmented single-celled conidia and conidiophores that slime down to form
glistening beads. Cladosporium (page 107) is prevalent in the air, and some species are plant or human
pathogens. This fungus has a highly branched conidiophore and one-or two-celled conidia that occur in
chains. Since all conidia of one species are not always of the same cell number or size, purity of a culture
cannot be determined by this means. Aureobasidium (page 71) is a filamentous yeast, hyaline when
young, becoming dark with age. Aureobasidium is often confused with species of Candida, but
pigmentation appears in its hyphae which is not found in Candida. One species, A. pullalans is
saprotrophic, but can become an opportunistic pathogen of plants. This same fungus is also known to be
a major agent in the deterioration of painted surfaces. Many species of Helminthosporium (page 125) are
well known to plant pathologists as pathogens of grasses. These fungi produce dark cylindrical conidia,
which are multiseptate and usually have rounded ends. The conidia of Bipolaris (page 127) and
Dreschlera (page 123) are nearly identical to those of Helminthosporium but differ in the mode of
conidial formation. The ends of the conidia vary only slightly making the differentiation of species
between Bipolaris, Dreschlera and Helminthosporium difficult. Illustrations along with the keys are most
helpful in correctly identifying species of these three genera. The most commonly encountered fungus in
the Dematiaceae is Alternar'ta (page 133), which produces large muriform conidia, often borne
acropetally in chains. Isolates of this fungus are readily recovered from air, soil, decaying vegetation and
from diseased potatoes and tomatoes.
Imperfect species which have conidiophores united in columns or clusters reside in the form family
Stilbaceae (pages 152 - 161). These multiple fused conidiophores are called synnemata or coremia and
tend to be more plentiful in aging cultures. The conidia are produced on the upper portions of the
synnemata. Some isolates of the Stilbaceae do not form synnemata on all media making identification
most difficult. Isaria spp. (page 157) are frequently isolated from soil and grow profusely on most
mycological agar media. One species, Pesotum ulmi, is well known to plant pathologists because it is the
imperfect form of the fungal pathogen that causes Dutch elm disease. The synnemata of P. ulmi are tall
and have a rounded mass of light-colored conidia embedded in mucilage.
The presence of sporodochia in the mycelium distinguishes form family Tuberculariaceae from the
other three form families of form order Moniliales. Refer to pages 146 - 151 and observe the many
different types of sporodochial fungi. A sporodochium is a cushioned-shaped structure made up of
closely grouped conidiophores. Definitive identification of sporodochial-producing fungi is often
difficult because the structures often vary with cultural conditions. Some, but not all species of Fusarium
(page 131), produce sporodochia. Species of Fusarium. are pathogens of humans, insects, plants and are
Catenulate conidia
conidiophore.
of
Penicillium sp.
on
phialides of a
xiii
Arthrospores of Geotrlchum sp.
abundant in the air and soil. It is easy to identify isolates to genus because of their characteristic bananashaped conidia. However the tremendous variability in conidial size, microconidia and macroconidia,
make them difficult to speciate. Species in the genus Epicoccum (page 151) are frequently isolated from
soil and decaying wood. This fungus has dark sporodochia, from which compact or loose conidiophorcs
give rise to dark, globose dictyospores (conidium has both oblique and transverse septa).
FORM ORDER SPHAEROPSIDALES
There are four form families in this form order and all of the species have well defined asexual fruiting
bodies i.e. pycnidia (page 162 through 187), Pycnidia are easily seen at low magnifications with a
compound or stereo-microscope. They have conidia which are either endogenously produced (inside the
pycnidium), or that differ from most other imperfect fungi and are exogenously produced. According to
Saccardo, the form families are differentiated as follows. Sphaeropsidaceae - dark pycnidia, leathery to
carbonaceous, which may or may not be produced on a stroma, usually having a circular opening;
Zythiaceae - physical characteristics as in form order Sphaeropsidaceae, but the pycnidia are brightcolored and waxy; Leptostromataceae - upper half of pycnidium fully developed, rather than in the basal
portion; Excipulaceae - Pycnidia are cupped or saucer-shaped. In this book, we do not separate pycnidia producing fungi using the four form families, although we may use a particular characteristic from a
given form family as part of the key composition.
Many members of the form order Sphaeropsidales are saprotrophic, although some are plant pathogens
and others infect insects and other fungi. Among the more common form genera are Phoma, (page 163),
Phyllosticta (page 163), Sphaeropsis (page 177), Coniothyrium (page 177) and Septoria (page 183).
Many of the species of these five genera are pathogens of plant stems and leaves. Problems in identifying
these fungi are obvious when comparing Phoma and Phyllosticta. Their pycnidia and conidia are so
similar that distinctions are at best arbitrary. Both have dark, erumpent pycnidia enclosing short
conidiophores that produce hyaline, non-septate conidia. Sphaeropsis is another form genus which is
similar to Phoma. Septoria (page 183) is a form genus with approximately 1,000 species, most being
plant pathogens. Many of the species names come from their hosts. Obviously, using the host to name the
fungal species leads to confusion, the proliferation of species, and questionable scientific designations.
The pycnidia of Septoria are dark, globose, ostiolate, erumpent; they enclose short conidiophores bearing
long, thin scolecospores. Therefore, the dark pycnidia are round, have an opening, and break out through
the surface of the substratum and produce endogenous narrow-elongate conidia.
Germinating
parium.
cralamydospores
of
Cylindrocladlum
sco-
xiv
Bristle-covered pycnidia of Chaetomella s p .
FORM ORDER MELANCONIALES
Species in this form order are recognized by a saucer-shaped fruiting body, the acervulus (page 188
through 195). There is only one form family, Melanconiaceae. Two common form genera are
Gloeosporium (page 189) and Colletotrichum (page 189). They are both very similar in appearance,
except that the latter has prominent dark setae associated with the conidiophores. The many species of
the two genera have conidia which are hyaline, one-celled, and ovoid to oblong. Under certain cultural
conditions, however, the setae of Colletotrichum fail to form, thereby making it impossible to distinguish
between the two genera. Glomerella, an ascomycete, is the teleomorph of both form genera which
indicates that, because of their similar anamorphic states, they should really be in one genus. Another
common genus is Pestalotia, which produces multiseptate conidia with pointed ends and apical
appendages (page 193). Species can be either pathogenic or saprotrophic. Careful scrutiny will show that
species of Cylindrosporium (page 193) are difficult to differentiate from species of Gloeosporium.
Similar appearing species of different genera present problems even to those who are familiar with the
fungi.
FORM ORDER MYCELIA STERILIA
Species placed here have no known anamorphic or teleomorphic states. They do however, produce
somatic sporodochium-like bodies, chlamydospores, sclerotia or bulbils. These diversified fungi are
grouped into approximately 20 genera and because of their heterogeneity there are no form families. No
asexual or sexual structures are found in these fungi, and therefore they are identified solely by mycelial
characteristics. Rhizoctonia and Sclerotium (page 197) are two common form genera, both containing
plant pathogenic species. Clamp connections on their hyphae provide evidence to basidiomycetous
affinities. Papulospora, another frequently encountered member of this form order produces bulbils
(shown on page 197) which are sclerotium-like and serve in survival and reproduction. Species of
Papulospora are saprotrophs of decaying vegetation and are pathogenic to storage structures of some
plants.
The imperfect fungi include a diverse array of fungi which occupy every conceivable ecosystem
within the Biosphere. There are aquatic and terrestrial species; some are saprotrophic, and some are
pathogenic to humans, animals, plants, microorganisms and to even other fungi. Their many spore and
somatic types have led to dispersal and invasion of may environments resulting in the evolution of this
highly diverse group of fungi.
xv
CYTOLOGICAL AND MORPHOLOGICAL
F E A T U R E S OF IMPERFECT FUNGI
The eucaryotic cellular structure, composition and ultrastructure of the imperfect fungi (DeuterOmycetes) have been thoroughly investigated using light and electron microscopy (4, 5, 7, 8, 11, 12). Cells
of imperfect fungi, like most fungi, are arranged in filaments or threads called hyphae. One filament of
the hyphae is a hypha, and all hyphae of one fungus constitutes the mycelium. Fungal hyphal cells vary in
size, color and in their extracellular matrix, when present. However, since hyphae among different kinds
of fungi are more alike than different, they usually cannot be used as a differentiating character.
The cells of a hypha are separated from one another by crosswalls called septa. Imperfect fungi have
one, two or more nuclei in their septate hyphal cells and can possess mitochondria, endoplasmic reticuli
with ribosomes, microtubules, Golgi bodies, vacuoles, glycogen and lipid. Woronin bodies and Spitzenkorpers (8), which are unique structures involved in apical hyphal growth may also be present. Often,
mitochondria and Golgi bodies are found to be closely associated in the cytoplasm. This ultrastructural
feature has been seen only in imperfect fungi and ascomycetes. Consequently, this association suggests a
relationship unique to these fungi that differentiates them from other fungi and other life forms (13).
Therefore, they have cells, organelles and inclusions similar to, yet different in some respects, from
protists, metaphytans and metazoans. The asexual spores of deuteromycetes, the conidia, contain similar
organelles and inclusions. Under light microscopy however, the cytoplasm of the typical imperfect
fungus appears translucent and granular and lacking discernible nuclei, organelles or other inclusions.
The hyphae and conidia of Verticillium albo-atrum and V. nigrescens are representative of imperfect
fungi since they are uninucleate and possess most of the aforementioned intracellular structures within
their plasma membranes (3). Newhouse et al. found these typical organelles, along with mycoviruses in
the hyphal cells of Cryphonectria parasitica (14). The majority of fungal viruses do not appear to have
any deleterious affect upon fungi, but some can debilitate their hosts and cause changes in colony
morphology, growth rate and pigmentation. This can result in an infected fungal isolate having a cultural
appearance far different from other fungi of the same species. This is an important consideration in
fungal identification. Light microscopy of fungal cells reveals little cytological detail; however,
transmission electron microscopy (TEM) and scanning electron microscopy (SEM) show with clarity the
organelles, some inclusions, and nuclei within the fungal cell.
Alexopoulus et al. provide excellent information on fungal ultrastructure and cellular relationships of
many and diverse fungi (1). Under light microscopy, the nuclei and organelles of the imperfects are
minute and difficult to observe without killing the cells and applying one or more cytological stains.
Consequently, intracellular characteristics of the cell(s) are of no value for identification. There is one
notable feature of the hyphae that is easily seen with the light microscope and enables differentiation of
an imperfect fungus from a typical phycomycete. This structure is the septum which separates individual
hyphal cells. All imperfect fungi have septa, unlike most phycomycetes which are coenocytic (lack septa
and are multinucleate). Ascomycetous and basidiomycetous fungi also possess septa. Within the septum
there may be one or several pores which provide cytoplasmic continuity between cells. The pores are
easily observed via TEM but not with light microscopy. Transmission electron micrographs demonstrate
that nuclei and various organelles can traverse the pores thus moving from cell to cell. Woronin bodies or
septal pore plugs are known to block pores, especially in hyphal cells that are old or damaged. Imperfect
fungi with known ascomycetous teleomorphs usually have simple septa, whereas basidiomycetous
teleomorphs have much more elaborate and complex dolipore septa.
External to the plasma membrane of the hyphal cell is the cell wall. This is apparent by light
microscopy and by TEM. This of course is a major difference between metazoans and most protists
which lack cell walls. Metaphytans also possess cell walls, but the chemical composition of the
xvl
microbibrils is different. The imperfect fungal cell wall, in conjunction with microtubules and microfilaments that comprise the cytoskeleton, preserve the cytoplasmic integrity of cells and also determines
the shape of the hyphal cell. Hyphal cells of Sclerotium rolfsii possess an actin cytoskeleton (15).
Cell growth of the filamentous fungi occurs almost exclusively at the hyphal tip. Transmission
electron micrographs of the hyphal apex by Grove, 1978 (6), and Grove and Bracker, 1970 (7), show
apical vesicles which are spherical and membrane bound. The apical vesicles contain the necessary
elements for plasma membrane extension and cell wall synthesis. More recent studies by Wessels in 1986
(19) and 1988 (20) provide evidence that the hyphal tip is elastic but ultimately becomes rigid with age.
Hyphae are the microscopic somatic structures of fungi which are embedded in various organic,
substrates or in soils. It is the hyphae that absorb nutrients required for growth and reproduction. The
organization and size of the mycelium is predicated upon substrate availability and nutrient status. While
additional structures are not usually formed by growing hyphae, some fungi form discrete microscopic
and/or macroscopic somatic and reproductive structures. Hyphae of some fungi can develop two
dlifferent kinds of fungal tissues (plectenchyma). These tissues develop from the apical growth of the
hyphae. Prosenchyma tissue are evident by their loosely woven organization in which the hyphae are still
mostly discernible. When the hyphae are not discernible and the cells become plant-like, the tissue is
pseudoparenchyma. Many resistant and reproductive structures develop from the two types of plectenchymous tissue.
One type of somatic tissue structure is the rhizomorph which results from the thickening of the
hyphae. Sclerotia (page 97) and microsclerotia are other structures in which the hyphae lose their typical
thread-like appearance and become a mass of cells which are resistant to various adverse conditions.
Another somatic structure, the stroma, is formed as a mass of fungal cells that usually supports various
types of reproductive structures. Rhizomorphs, sclerotia, microsclerotia and stroma are important structures in determining the type and, in some few instances, the identity of an unknown fungus. The more
identifiable structures (mainly reproductive, but also somatic) that can be determined for an unknown
fungus, the easier it will be to identify.
The conidial cells, their conidiophores, acervuli, pycnidia, sporodochia, synnemata and chlamydospores are other cellular structures of imperfect fungi which are easily discernible with the light microscope, and are routinely used in identification. These structures are illustrated and discussed throughout
this book. Complete familiarity with these structures will facilitate use of the keys for identifying
unknown imperfect fungi.
xvii
FACTORS AFFECTING GROWTH AND
SPORULATION OF I M P E R F E C T FUNGI
The imperfect fungi are adapted to live under diverse environmental and nutritional conditions.
Conidia of some species often survive for years in a cold or dry environment and germinate upon
exposure to favorable conditions. The conditions that favor or inhibit growth and sporulation of a given
fungus are correlated with its habitat. For example, Bispora, which obtains its nutrients from decaying
wood, is limited in growth only by temperature and moisture, whereas, other fungi have more precise
requirements, such as for living tissue or preformed vitamins. In fact, the dissemination of plant
pathogenic conidia is often limited to the growing season of the host plant, and the production of conidia
at that time. This and other types of adaptation have led to the survival of the deuteromycetes that exist
today. Several types of fungal responses to nutrition and environment are presented.
TEMPERATURE
Temperature and moisture are universal factors that affect all organisms and must be favorable for
them to survive, grow and reproduce. The cardinal temperatures i.e. minimum, optimum, and maximum,
are used to describe the range at which individual imperfect fungi can grow. The exact ranges are
influenced by other factors. There is a great variation among the responses to temperature of the
imperfect fungi; however, they all produce some growth at mesophilic temperatures. When growing
unknown, fungi it is best to select a temperature between 20 and 30 degrees Centigrade for their initial
incubation.
MOISTURE
Imperfect fungi are capable of growing in liquid nutrient solutions provided that sufficient oxygen is
present. However, many deuteromycetes can grow in the absence of liquid water. Botrytis cinerea and
Penicillium expansum are plant pathogens which cause rots of plant parts and obtain moisture from the
decomposing plant cells. Species of Aspergillus, Penicillium, Cladosporium, and Aureobasidium are
common decomposing agents of cloth, paper, leather, wood and even painted surfaces where there is no
free moisture. Aspergillus and Penicillium spp. proliferate in stored grains when the moisture content is
greater than 14%. Another Aspergillus sp., A, glaucas and its close relatives are well known for their
ability to grow under conditions of severe physiological drought.
In contrast there are the many imperfect species that cannot grow without liquid water or a saturated
atmosphere. Spores of most deuteromycetes require moisture for germination.
LIGHT
Imperfect fungi respond to light (radiation) in a myriad of ways, but are not photosynthetic. Like all
fungi they are incapable of reducing C0 2 to carbohydrate via radiation. Nevertheless, phototropic growth
of conidiophores has been amply demonstrated for Aspergillus giganteus, A. clavatus, Penicillium
claviforme and numerous other fungi. When cultures receive unilateral illumination, the conidiophores
grow toward the white light, irrespective of the position of the culture. Certain frequencies of radiation
are also known to enhance or be necessary for the induction of sexual structures of imperfects having
known teleomorphic states. Radiation also may affect the chemical composition of media thereby
promoting growth patterns different from those that would occur when the media were stored in the dark.
xvlii
Radiation has the greatest impact on sporulation of imperfect fungi. Sporulation of imperfects is either
induced (i.e., light is necessary) or enhanced by exposure to different wavelengths of radiation.
Ultraviolet, near ultraviolet, blue (most common), a wide band of blue-green-yellow and far red all affect
fungal sporulation, albeit, quite differently. The red band is seldom effective for inducing sporulation.
White light may be as effective as any given color if the intensity is nearly equal. The intensity of
white light necessary for sporulation by Epicoccum nigrum varied inversely with duration of exposure.
An exposure of mycelial cultures on agar to sunlight (7,000 ft. candles) for 15 minutes induced the
production of about as many conidia as a single exposure of 24 hours at 50 ft candles or 6 hours at 100 ft.
candles. Spores were produced only in the zone of young hyphae at the time of exposure. It is well
known that ultraviolet radiation is inhibitory, yet there are few^ concrete examples of inhibition of
imperfect fungi by visible light. Remember, when growing imperfects which do not sporulate in culture,
the absence of light or too little of it, may be an important factor. In general, expose fungal cultures to
alternating periods of light and dark to induce sporulation.
HYDROGEN-ION CONCENTRATION (pH)
Most fungi grow optimally when the substrate is slightly acid between pH 5.0 and 6.0. However, they
will generally achieve fair to good growth over a much wider range, from about pH 3.0 to 8.0. Certain
species are able to tolerate even greater ranges: Aspergillus niger, pH 2.8 to 8.8; A. oryzae, 1 . 6 to 9.3;
PenicilUum italicum, 1 . 9 to 9.3; Fusarium oxysporum, 1 . 8 to 11.1; Botrytis cinerea, 2.8 to 7.4; and
Rhizoctonia solani, 2.5 to 8.5. When fungi are growing on most culture media, they alter the pH of the
substrate. The extent of the pH change depends on the composition of the substrate as well as on the
genetics of the imperfect fungus.
CARBON AND NITROGEN SOURCES
The requirement of fungi for carbon is greater than any other nutrient, however a source of nitrogen
must also provided. The ubiquitous nature of most deuteromycetes indicates that they possess the genetic
determinants (synthesis of enzymes) to utilize carbon from many different sources; among these,
cellulose is the most abundant utilizable source. Seldom does a fungus in nature encounter a pure carbon
source, but rather will preferentially select from what is available.
To determine the ability of specific fungi to utilize single carbon sources, experiments in the
laboratory must be conducted under controlled conditions, using a medium that is complete for all
nutrients except carbon. Imperfect fungi respond to different carbon sources, and their preferred source is
usually associated with the niche they occupy in the ecosystem. Growth on glucose, fructose and
mannose are approximately the same for all fungi. Most natural media have more than one carbon source
from which a fungus can obtain carbon requirements for growth and reproduction.
In nature, organic materials provide the nitrogen needed for growth; however, most fungi can use
sources of inorganic nitrogen as well. Most imperfect fungi utilize nitrate, ammonium and amino acids as
sources of nitrogen. Growth on inorganic nitrogen is often less than on a mixture of amino acids or on a
complex organic nitrogen source. If one merely desires to cultivate deuteromycetes on a laboratory
medium, yeast extract or casein hydrolysate is excellent. To study the relative rate of utilization of
nitrogen sources, one should use single amino acids, such as asparagine, aspartic acid or glutamic acid.
VITAMINS
Most imperfect fungi are capable of synthesizing required vitamins from living or non-living
substrates. Some imperfects, however, are deficient and cannot synthesize certain vitamins. Such
deficiencies can be determined only by cultivation in suitable synthetic media with and without added
vitamins. When imperfects are vitamin-deficient, it is usually thiamine that they are unable to synthesize.
A deficiency may be single or multiple, complete or partial. Most species of Aspergillus synthesize all
XIX
required vitamins. Botrytis cinerea, species of Penicillium, Cylindrocladium scoparium, Gliocladium
roseum and other imperfect fungi are also able to synthesize their vitamin requirements. The pycnidial
producer, Dendrophoma obscurans, must have a preformed source of thiamine as do some species of the
dermatophyte genus, Trichophyton. Biotin is needed for Diplodia macrospora and for Stachybotrys atra.
INORGANIC SALTS AND MICROELEMENTS
Natural organic compounds often furnish all of the inorganic salts necessary for growth. However, if
one needs to culture imperfects on synthetic or semi-synthetic media, it is necessary to add certain
compounds. Monobasic potassium phosphate (KH 2 P0 4 ) and magnesium sulfate (MgS0 4 ) will supply
potassium, phosphorus, magnesium and sulfur. The microelements Fe, Zn, Mn, Cu and Ca are frequently
added to synthetic media to supply additional inorganic elements needed for optimal fungal growth.
ISOLATION, CULTURE MEDIA, MAINTENANCE OF STOCK CULTURES,
AND PHYSIOLOGY
Information on these topics can be found on pages 1-3.
xx
REFERENCES CITED
1. Alexopoulus, C. J., C, W. Mims and M. Blackwell. 1996. Introductory Mycology. John Wiley &
Sons, New York.
2. Barron, G. L. 1968. The Genera of Hyphomycetes from Soil. Williams & Wilkins, Baltimore, MD.
3. Buckley, P. M., T. D. Wyllie and J. E. DeVay. 1969. Fine structure of conidia and conidium
formation in Verticillium albo-atrum and V. nigrescens. Mycologia61: 240-250.
4. Farley, J. F., R. A. Jersild and D. J. Niederpruem. 1975. Origin and ultrastructure of the intra-hyphal
hyphae in Trichophyton terrestre and T. rubrum. Arch. Microbiol. 43: 117-144.
5. Griffiths, D. A. 1973. Fine structure of the chlamydospore wall in Fusarium oxysporum. Trans. Br.
Mycol. Soc. 6 1 : 1-7.
6. Grove, S. N. 1978. The cytology of hyphal tip growth, In: The Filamentous Fungi, (Vol. 3). Smith,
J. E. and D. R. Barry, Eds. John Wiley & Sons, New York.
7. Grove, S. N. and C. E. Bracken 1970. Protoplasmic organization of hyphal tips among fungi:
Vesicles and Spitzenkorpers. J. Bacterio], 104: 989-1009.
8. Howard, R. J. 1981. Ultrastructural analysis of hyphal tip growth in fungi: Spitzenkorper,
cytoskeleton and endomembranes after freeze substitution. J. Cell Sci. 48: 89-103.
9. Hughes, S. J. 1953. Conidiophores, conidia and classification. Can. J. Bot. 3 1 : 577-659.
10. Hunter, B. B. and H. L. Bamett. 1973. Deuteromycetes (Fungi Imperfecti), In: Handbook of
Microbiology: (Vol. 1), Organismic Microbiology. Laskin, A. I. and H. A. Lechevalier, Eds. CRC
Press, Cleveland, OH.
11. Hunter, B. B. and H. L. Bamett and T. P. Buckelew. 1978. Deuteromycetes (Fungi Imperfecti), In:
Handbook of Microbiology: (Vol. 2), Fungi, Algae, Protozoa, and Viruses. Laskin, A. I. and H. A.
Lechevalier, Eds. CRC Press, West Palm Beach, FL.
12. Mims, C. W. 1991. Using electron microscopy to study plant pathogenic fungi. Mycologia 83:1-19.
13. Newhouse, J. R„ H. C. Hoch and W. L. MacDonald. 1983. The ultrastructure of Endothia parasitica.
Comparison of a virulent with a hypovirulent isolate. Can. J. Bot. 6 1 : 389-399.
14. Newhouse, J. R., W. L. MacDonald and H. C. Hoch. 1990. Virus-like particles in hyphae and conidia
of European hypovirulent (dsRNA-containing) strains of Cryphonectria parasitica. Can. J. Bot.
68:90-101.
15. Roberson, R. W. 1992. The actin cytoskeleton in hyphal cells of Sclerotium rolfsii. Mycologia 84:
41-51.
16. Roper, J. A. 1966. The parasexual cycle, In The Fungi, (Vol. 2). Ainsworth, G. C. and A. S.
Sussman, Eds. Academic Press, New York.
XXI
PARTI
PHYSIOLOGY
ISOLATION
Many different techniques for the isolation of fungi in pure culture have been described (246, 390).
One should select and try first a method that is simple and easy, using a general purpose medium. Many
species, especialJy common .saprophytic hyphomycetes, sporulate readily in a moist chamber on pieces of
wood, leaves, or other plant pans. Conidia may be lifted from the sporulating conidiophores by touching
with a small bit of agar on the tip of a needle, while looking through a stereoscopic microscope. This
simple method often results in a high percentage of cultures free of contamination. It can also be used to
obtain conidia from oozing acervuli or pycnidia. Species growing in habitats with an abundance of
bacteria may require the use of dilution plates or antibiotic agar (219). A water agar substrate may even be
useful, but a rose bengal streptomycin agar has been recommended (390). A highly specialized medium
containing antibiotics was used for isolation of Vertirtcladiella procera from diseased pine roots (428).
The use of geranium leaves placed on the soil surface has been recommended for recovering species of
Cylindrocladium from soil (310). Botrytis cinerea and other soft rot fungi can be obtained easily in pure
culture by passage through apples or other fruits. Pathogenic fungi within plant tissue often require
surface sterilization with 10% chlorox for 2 minutes before plating the material on agar (246). The
common method of obtaining the oak wilt fungus from diseased trees was stripping bark from twigs,
dipping in 95% alcohol, and flaming (445). Wood chips were then plated on agar.
The necrotrophic mycoparasites, such as Gliociadium roseum and species of Trichuderma, do not
require a special medium for isolation. However, the biotrophic mycoparasites are a highly specialized
group in regard to nutrition, are usually isolated with a host species, and are best maintained as twomem be red cultures.
Nematode trapping fungi may often be obtained by placing a bit of horse manure or soil rich in
humus on an agar plate. Nematodes are usually abundant after a few days and the trapping fungi, if
present, should appear a few days later. Transfers from pure cultures of these species to the plates with
nematodes will assure the formation of the characteristic loops, rings, or nets. Common species belong to
the genera Arthrobutrys, Dactylella, Monacrosporium, or close relatives (106).
Conidia of Bispora sp. Note the formation of a new
conidium at the apex of the con i d i a l chain.
A synnematous fungus (Briosia sp.) growing from
decayed vegetation.
1
2
PHYSIOLOGY
CULTURE MEDIA
A satisfactory general culture medium must contain all of the nutrients required by the fungus:
utilizable carbon and nitrogen sources, certain salts and microelements, and water. Some species are
favored by added vitamins or growth factors. Many plant parts or products contain these nutrients but
not always in quantities optimum for growth or sporulation. A potato-dextrose (glucose) agar medium
has been the favorite of many plant pathologists for many years. Other natural media have been
developed and used by mycologists for specific fungi. A list of one hundred media is given in the
Mycological Guidebook (390). The authors prefer a general medium containing 5 to 10 g glucose, I to 2 g
yeast extract, and 1000 ml water. Addition of agar and changes in concentrations may be made as desired.
This medium is easy to make, and the pH need not be adjusted.
The use of a synthetic medium, in which each nutrient and its concentration is known and can be
altered as desired, is preferred in critical studies of fungus physiology. Such media can be duplicated
exactly, and the effects of each nutrient can be measured. One satisfactory synthetic medium contains
glucose (5 to 10 g), KN0 3 . asparagine or glutamic acid (1 to 2 g), KH 2 P0 4 (1.0 g), MgS0 4 (0.5 g),
microelements (Fe, Mn, Zn) (trace), and distilled water (1000 ml). Vitamins thiamine (100 /jg). biotin (5
fig), and pyridoxinc (JOO/ig) may be added routinely for the deficient species (259). This liquid medium
may be used in flasks, or agar may be added for tube or plate culture, Five species of biotrophic
mycoparasites require the new growth factor mycotrophein, which is a naturally occurring product in
most filamentous ascomycetes and imperfects. It may be obtained in crude form by extracting from the
mycelium with hot water (10, 12, 48, 138, 220,469).
MAINTENANCE OF STOCK CULTURES
The choice of a method for keeping viable cultures over a long period of time depends on the period of
time they are to be maintained and the convenience of the method (259). Frequent transfer of mycelium
from a culture to a fresh agar slant in test tubes is satisfactory for short periods. Long term maintenance of
viable mycelium can be accomplished using screw-cap test tubes. Allow mycelium to grow until it reaches
the edge of the agar slant, then screw the caps down tightly and store at about 5 UC. Transfer cultures after
6 to 12 mo. The use of screw cap tubes has the additional advantage of excluding mites. Many eonidia
remain viable for months when collected and stored dry at low temperatures, or simply frozen. Mycelium
of some fungi may be cultured on bits of wood or other plant tissue and stored dry-
Fruiting structures of Cylindrocladium parvum growing in
culture.
Conidial heads of Aspergillus niger.
PHYSIOLOGY
3
PHYSIOLOGY: NUTRITION AND ENVIRONMENT
See references 141, 157, 162, and 259 for textbooks on fungus physiology.
The same nutrients that favor vegetative growth are also generally favorable to sporulation, but often in
different concentrations or ratios. A low concentration of available carbon usually favors sporulation.
Sporulation by species pycnidia is often delayed until growth reaches a maximum.
Among the common carbon sources, glucose, fructose, mannose, and maltose are utilized most readify;
xylose and sucrose intermediately; whereas lactose and sorbose are often poorly utilized or not at all.
The table lists as examples the relative amount of vegetative growth of selected species on several sugars
(3 = good to excellent; 2 = fair; 1 = poor; 0 = not utilized) (218).
Alternaria solani
Aspergillus niger
Colletotrichum lindemuthianum
Cordana pauciseptata
Dendrophoma obscurans
Helminthosporium sativum
Penicillium expansum
Rhizoctonia solani
Thielaviopsis basicola
Choanephora cucurbitarum
A = days
B = glucose, fructose, mannose
C = galactose
D = sorbose
A
B
14
3
7
3
3
14
14
3
14
3
7
3
4
3
5
3
7
3
3
3
E = xylose
F = maltose
G = sucrose
H = lactose
C
3
2
3
3
3
2
2
3
3
3
D
1
2
0
0
1
1
3
0
0
0
E
3
3
1
3
2
2
3
3
0
I
F
3
3
2
1
2
3
3
3
3
3
G
2
3
2
1
2
3
3
3
3
0
H
2
1
2
1
2
2
1
2
0
0
Temperature is a universal factor affecting all physiological processes in fungi, most of which grow w
well
within a range of 25 to 30 °C, but there is much variation. The approximate cardinal temperatures are
given below for selected species (218).
Aspergillus fumigatus
Botrytis cierea
Diplodia zeae
Epicoccum nigrum
Helminthosporium sativum
Humicola grisea v. thermoides
Rhizoctonia solani
Trichothecium roseum
Verticillium albo-atrum
Minimum
<20
0
10
< 5
< 5
24
2
<10
5
Optimum
35
20
30
25
25-30
38-46
25-30
30
25
Maximum
50
30
35
35
35
56
35
35
35
Visible white light may affect imperfect fungi in different ways. Some species show a decided positive
phototropism of the conidiophores (e.g., Aspergillus giganteus, A. clavatus, and Penicillium claviforme).
The conidiophores grow directly toward the source of light, regardless of the position of the culture (259).
Sporulation of a number of species of imperfects is either induced (light is essential) or favored
(increased) by exposure of the mycelium to radiation. In general, only the mycelium that is young at the
time of exposure responds to radiation. Different species respond to different wave lengths, blue being the
most effective range for most fungi. Some species that respond to exposure to white light or to specific
wave lenghths are: Botrytis cinerea (uv), Cylindrocladium citri (blue to far red), Cyllndrocladium spp. (uv,
near uv, blue), Dendrophoma obscurans (blue), some isolates of Epicoccum nigrum (uv), Helminthosporium vagans (near uv), and Trichoderma lignorum (blue). The intensity of white light required to
induce sporulation by one isolate of Epicoccus nigrum varied inversely with the duration (430). Note that
a long exposure to intense ultraviolet radiation is lethal to fungus mycelium.
4
PHYSIOLOGY
USE OF IMPERFECT FUNGI TO ILLUSTRATE BIOLOGICAL PRINCIPLES
Certain species work well in demonstrating the effects of nutritional and environmental factors on
growth and sporulation. A few demonstrations that can be easily performed in the classroom, together
with the species used, are suggested below.
Effects of white light on production of conidia: Trichoderma Ugnorum, Epicoccum nigrum (390).
Inoculate plates of general purpose agar at the center with conidia or mycelium. Place some cultures incontinuous light, some in alternate light and darkness, and some in total darkness at 20 to 25 °C. Examine
after 4 to 6 days. E. nigrum may also be used to demonstrate an inverse intensity-duration relationship
required for sporulation (i.e., long exposures at low intensity compared with short exposures at high light
intensity (429). Try a range from 5 to 1000 footcandles.
Positive phototropism of conidiophores: Aspergillus clavatus. Inoculate several plates of general
purpose medium with conidia. Place some cultures beneath continuous light, some with single directional
light, and some in total darkness. Wrap some in light-tight paper or foil, and cut one or two small
windows. Examine after 4 or 5 days.
Effect of color (wave length) of light on fruiting: Dendrophoma obscurans (32). Place cultures of this
fungus under white light, under blue, yellow, green, and red filters, and in darkness. Examine after 7 days.
Natural products may replace the light requirement for production of pycnidia: Dendrophoma
obscurans. Use a synthetic agar medium with thiamine. Place on some plates autoclaved strawberry
leaflets on the surface of the agar. Incubate cultures in alternate light (50 footcandles or more) and
darkness for a few days, and examine for pycnidia.
Special light requirements for production of conidia: Choanephora cucurbitarum (11). Use plates of
glucose-asparagine agar plus thiamine. Petri dishes with loose-fitting lids will allow adequate aeration.
Place cultures under the following conditions: continuous light; continuous darkness; 2 days light —
12 hours darkness; 2 days darkness — 12 hours light. Examine for conidia in 3-day-old cultures.
Need for adequate aeration for production of conidia: Choanephora cucurbitarum. This can be done
simultaneously with the light requirement demonstration. Provide adequate aeration of some of the
cultures by using loose-fitting lids, and prevent exchange of gases in other cultures by taping dishes closed
(II). Incubate in alternate light and darkness.
Sugar concentration affects growth of mycelium and production of conidia: Helminthosporium
sativum, Choanephora cucurbitarum, or Mektnconium JuKgenium (or other species sporulating readily).
Use a glucose-yeast extract medium, with glucose concentrations of 1, 5, 20, and 5 g/liter.
Sugar concentration affects size of conidia: Helminthosporium victoriae (or some other species of this
genus) (110). Prepare the same medium as above, and measure the length of conidia formed at the
different concentrations.
Thiamine deficiency: Dendrophoma obscurans or Choanephora cucurbitarum (11). Use a liquid
glucose-asparagine medium (see section on media above) in small flasks (25-ml to 250-ml flasks are
satisfactory). To half of the medium add thiamine at the rate of 1 0 0 //g/liter. Observe growth daily. If an
accurate measure of growth is desired, the mycelium can be collected on a cloth or filter paper, dried and
weighed.
Biotin deficiency: Diplodia macrospora (259). Repeat above procedure, except use biotin at the rate of
5 ^g/liter.
Multiple deficiency for thiamine and biotin: Arthrobotrys musiformis. Use the same basal medium as
above; add vitamins singly and in combination, using basal medium as control.
Pyridoxine deficiency: Graphium sp. (9). Use the same basal medium as above, adding pyridoxine at
the rate of 1 0 0 /ig/liter.
PHYSIOLOGY
5
Destruction of pyridoxineby Ijght(9): Graphiumsp. Preparea medium containing pyridoxine (liquid
or agar). Store part of the medium under continuous bright light, and the remaining medium under total
darkness for 10 to 14 days, Inoculate both media, and observe growth,
Trapping and consuming small nematodes (106). Arthrobotrys spp. Use of a glucose-yeast extract
medium is suggested. Nematodes can be obtained easily by placing a bit of horse manure on agar plates.
After a few days use a stereoscope to check for the presence of Arthrobotrys. If none is present, use pure
culture of fungus to inoculate cultures of the nematodes. Observe after a few days for rings, nets, or other
traps and for trapped nematodes.
Necrotrophic mycoparatism: Trichoderma lignorum, Gtiochdium roseum (10, 13). Prepare
3- to 5-day-old cultures of several common fungi. Inoculate these cultures at the edge of the mycelium
with one of the above suggested species. Observe daily for the parasite overgrowing the host colony, and
examine microscopically for destroyed host cells.
PART II
TAXONOMY AND IDENTIFICATION
THE SACCARDO SYSTEM OF CLASSIFICATION
The Saccardo System has long been in use for the classification of imperfect fungi. The primary basis
of this system is the morphology of the sporulating structures as they are known in nature, as well as the
morphology and pigmentation of conidia and conidiophores. In artificial culture, some species of
imperfects fail to form typical fruiting structures (e.g., acervuli. sporodochia. and synnemaia).
Although an alternate system of classification may be more convenient for mycologists who have
studied the different methods of conidium development, the authors recommend that others use the
illustrations and key based on the Saccardo System. Moniliaceac and Dcmatiaceae, the two largest
families, are presented according to the Hughes-Tubaki-Barron System of Classification beginning on
page 41.
ORDERS INCLUDED
Conidia! Phycomycetes. Mycelium typically coenocytic; septa absent or infrequent; conidia (sporangioles) present; typical large, muUispored sporangia may also be present in some genera. This group is
included here because of similarity to some genera of the imperfect fungi.
MUCORALES
8
Mostly saprophytic, but some species parasitic on plants or other fungi.
Fungi Imperfeeii. Mycelium (if present) typically septate with frequent septa; conidia normally present
except in a few genera. Classification and identification are based on the conidial state, although the
perfect state is often known and sometimes also present.
Fruiting heads of Verticlciadielia procera.
Synnemata and conidia of the Dutch elm fungus, Pesotum
ulmi.
6
TAXONOMY AND IDENTIFICATION
SPHAEROPSIDALES
7
28
Conidia produced in well defined asexual fruit bodies, pycnidia.
MELANCONIALES
33
Conidia typically produced in acervuli under natural conditions; in culture conidiophores may
be single or in compact groups, resembling sporodochia of the Moniliales.
MONILIALES
Conidia produced directly on the mycelium, on separate conidiogenous cells, or on distinct
conidiophores that may be separate, in clusters, or in tightly packed groups. This is the largest
and most common order.
MYCELIA STERILIA
34
No conidia produced. Usually sclerotia or other structures are formed for survival. This group
does not include those fungi that do not sporulate because of unfavorable nutritional or
environmental conditions.
FAMILIES OF MONILIALES
TUBERCULARIACEAE
25
Condiophores typically compacted into a rounded or flat sporodochium, often not well developed
in artificial culture. Some species of Melanconiales produce structures resembling sporodochia in
culture.
STILBACEAE
26
Condiophores typically compacted into synnemata, which may be more abundant in aging
cultures. Single conidiophores may also be present in some cultures or may be the only conidial
state present. Such cultures may be identified in one of the following families.
MONILIACEAE AND DEMATIACEAE
Conidiophores mostly single and separate or produced in loose clusters. These two families are
considered together because the only described difference is the hyaline conidia of the former and
the pigmented (dark) conidia or conidiophores of the latter. Conidia are considered pigmented if
the walls appear dark either separate or in mass.
Only within this order (Moniliales) are families used in the identification of genera.
In the Saccardo System orders and families may be broken into sections as follows: Amerosporae, conidia 1-celled; Didymosporae, conidia 2-celled; Phragmosporae, conidia with transverse
septa only; Dictyopsorae, conidia with both transverse and oblique septations; Scolecosporae,
conidia filiform; Staurosporae, conidia stellate or branched; Helicosporae, conidia typically
coiled. The prefixes Hyalo- and Phaeo- are sometimes added to each section name to indicate
hyaline or darkly pigmented conidia, respectively.
r
1 0 , 17
KEY TO GENERA
Note that there is a separate key for each order.
MUCORALES
la Conidia (sporangioles) globose, borne singly on apex of conidiophores
(sporangiophores) or branches
Mortierella
60
lb Conidia (sporangioles) globose to elongate, borne in clusters or in heads
2
2a Special spore-bearing branches (sporocladia) bearing conidia only on one side
(upper or lower)
3
2b Sporocladia not present
7
3a Sporocladia borne on coiled or recurved branches
4
3b Sporocladia not on coiled or recurved branches
5
4a Sporocladia on coiled branches; conidia short ellipsoid
4b Sporocladia in umbels on recurved branches; conidia obovoid
4c Sporocladia arising from loosely spiraled branches; conidia globose
to subglobose
Spirodactylon
64
Martensiomyces
64
Spiromyces
66
5a Conidia borne only on upper (inner) side of sporocladium
6
5b Conidia borne only on lower (outer) side of sporocladium
Coemansia
62
6a Conidiophore simple, bearing a few lateral or apical sporocladia
Martensella
64
6b Conidiophore simple, bearing a whorl of sporocladia on an apical disc
Kickxella
64
6c Conidiophore long, branched, bearing lateral, dome-shaped sporocladia
Linderina
64
7a Conidia produced in rows, or sporangioles in chains, often breaking up into rows
of spores
7b Conidia not in rows (chainlike); sporangioles do not break up into rows of spores
8a Conidiophores nonseptate, simple or branched; conidia radiating apex
8
12
9
8b Conidiophores septate, distinctly branched
10
9a Conidiophores simple, with basal rhizoids
9b Conidiophores usually branched; rhizoids absent
10a Conidiophore branches dichotomous, all fertile
10b Conidiophore branches verticillate, all fertile
8
Syncephalis
62
Syncephalastrum
66
Piptocephalis
62
Dimargaris
62
MUCORALES
10c Conidiophore branches irregular, some with sterile tips
1 la Fertile branches enlarged, bearing a head of cylindrical conidia
1 lb Fertile branches repeatedly branched; conidia not in compact heads
9
11
Dispira
66
Tieghemiomyces
62
12a Conidiophores with lateral or terminal branches
13
12b Conidiophores simple
14
13a Spore-bearing head compound; conidia ellipsoid, usually colored
13b Spore-bearing head compound; conidia hyaline, reniform to ellipsoid
13c Spore-bearing head simple; conidia hyaline, globose to subglobose
Choanephora
66
Radiomycea
64
Cunninghamella
60
14a Conidia not produced in slime, dry
15
(4b Conidia produced in slime drop in a head
Helicocephalum
60
J 5a Conidia borne on enlarged globose apex
Rhopalomyces
60
Mycotypha
60
15b Conidia borne on cylindrical upper portion of conidiophore
MONILIALES
la Conidia more or less coiled or spirally curved, hyaline or dark (parts of Moniliaceae,
Dematiaceae and Tuberculariaceae)
2
10
lb Conidia not coiled
HELICOSPORES
2a Conidiophores forming a sporodochium
3
2b Conidiophores single or in loose clusters
4
3a Conidial coil flat; sporodochium stalked
Everhartia
150
3b Conidial coil in a loose spiral; sporodochium not stalked
Hobsonia
150
4a Conidial coil more or less flattened
5
4b Conidial coil spiral
9
5a Conidia thick in proportion to length
6
5b Conidia slender
8
6a Conidia hyaline or dark, with transverse septa only
7
6b Conidia dark, with transverse and oblique septa
C_7a /Parasitic on higher plants
Xenosporium
136
Helkomina
136
7b Saprophytic on wood or bark
Helicotna
136
8a Conidiophores hyaline, short
Helicomyces
136
10
KEY TO GENERA
8b Conidiophores pigmented, pale or dark, tall
Helicosporium
136
Helicoon
136
Helicodendron
136
10a Both conidia and conidiophores (if present) hyaline or brightly colored; conidiophores
single or in loose clusters
Moniliaceae
11
10b Either conidia or comdiophores (or both) with distinct dark pigment; comdiophores
single or in loose clusters
Dematiaceae
105
10c Conidiospores compacted into sporodochia
Tuberculariaceae
202
Stilbaceae
225
9a Conidia borne singly
9b Conidia catenulate
NOT HEUCOSPORES
lOd Conidiophores typically united into synnemata
MONILIACEAE
11a Conidia typically 1-celled, globose to several times longer than wide
12
1! b Conidia typically 2-cellcd, mostly ovoid to cylindrical
62
11 c Conidia typically 3- or more-celled, shape variable
74
12a Conidiophores absent or like the mycelium, or reduced to phialidcs or peglike
denticles
13
12b Conidiophores distinct, although sometimes short
19
V 13a Pathogenic to humans
14
13b Saprophytic or parasitic, mostly soil or on plant parts
15
14a Filamentous in cultures at 25°C, with large chlamydospores.. Blastomyces, Histoplasma 80, 82
I4b Both filamentous and yeastlike cells at 25 °C, without large chlamydospores
15a Conidia (arthrospores) segment from branches of conidiophores,
rounded
Candida
70
Chrysosporium
68
15b Conidia (arthrospores) formed by segmentation of hyphae, rod-shaped — Geotrichum ,
68
15c Conidia not arthrospores, not formed by segmentation
16
16a Setae absent
17
16b Setae present, mostly circinate, unbranched
Circinotrichum
90
16c Setae present, branched, circinate or wavy
Gyrothrix
90
17a Mycelium with clamp connections
Itersonilia
70
17b Mycelium without clamp connections
18a Conidia produced on sterigmata and forcibly discharged
18
Sporobolomyces
18b Conidia borne on sides of mycelium or formed by budding, not forcibly
discharged
Candida
70
70
19a Conidial state of powdery mildew; conidia catenulate
19b Conidial state of powdery mildew; conidia not catenulate
MONIUALES
11
Oidium
68
Ovulariopsis
70
19c Not conidial state of powdery mildew ,
20
20a Conidia distinct in shape from apical cells of conidiophore
21
20b Conidia (arthrospores) gradually become rounded from apical cells of
conidiophore
Wallemia
92
Monilia
72
Tilletiopsis
12
21a Conidiophores (or phialides) typically simple or with few branches; phialides, if present,
not tightly clustered into heads
22
21b Conidiophores mostly branched; phialides, if present, clustered into groups or heads —
38
22a Conidia catenulate
23
22b Conidia not catenulate
29
23a Conidia endogenous; phialides prominent, simple
24
23b Conidia exogenous; conidiophores simple or branched
26
20c Conidia (blastospores) globose to ellipsoid, similar to apical cells of
conidiophore
20d Conidia (blastospores) elongate, slender, much like cells of conidiophore
24a Dark aleuriospores (chlamydospores) present, rounded, usually single
24b Dark aleuriospores (chlamydospores) in short chains of truncate cells,
breaking up
Chalaropsis
90
Ihielaviopsis
92
24c Dark aleuriospores rarely formed
25
25a Dark setae present
Chaetochalara
90
25b Dark setae absent
Chalara
90
26a Conidia blastospores or botryoblastospores
27
26b Conidia otherwise
28
27a Conidia in chains on slender conidiophores
Hyalodendron
72
Gonatorrhodiella
78
Monocillium
86
28b Conidia arthropsores, nearly globose with a flat base
Basipetospora
70
28c Conidia arthrospores, rod-shaped
Oidiodendron
68
Chrysosporium
68
Tritirachium, Beauveria
100
27b Conidia on enlarged apex and nodes of conidiophores
28a Conidia phialospores; phialides simple
29a Conidiophores or conidiogenous cells short or indefinite
29b Conidiophores or conidiogenous cells distinct; fertile portion
rachislikc
29c Conidiophores or conidiogenous cells distinct, fertile portion not rachislike
30
30a Conidiophores not inflated or only slightly so
31
30b Conidiophores or fertile cells distinctly inflated at middle or apex
37
12
K E Y TO GENERA
31a Conidia curved; aquatic on dead leaves
Lunulospora
138
31 b Conidia globose to ovoid; not aquatic
32
32a Conidia sympodulospores
34
32b Conidia aleuriospores
35
32c Conidia blastospores or phialospores; single
33
33a Conidia blastospores, on long denticles, dry
Otpitrichum
33b Conidia phialospores, in moist heads
36
34a Conidiophores clustered
Ovularia
34b Conidiophores single, separate
35a Conidiophores single, simple, forked at apex
35b Conidiophores usually have branches arising from an enlarged cell
35c Conidiophores with variable short lateral branches
74
104
Sporothrix
98
Glomerularia
86
Umbelopsis
86
Staphylotrichum
80
Vertkillium
92
36b Conidiophores in acervuli in nature; in culture, conidiophores separate or in poorly
formed groups
Gloeosporium
188
36a Conidiophores branched verticillately
36c Conidiophores simple or with few branches, never in acervuli
Cephalosporium
94
37a Fertile cells globose; conidiophores short, stout
Phymaiotrkhum
78
37b Fertile cells globose, single, apical; conidiophores slender
Oedocephalum
76
37c Fertile cells globose, apical and intercalary
Gonatobotrys
76
37d Fertile cells somewhat elongated; conidia borne on short denticles
Rhinotrichum
76
Acladium
76
Fertile cells elongated, cylindrical, enlarged branches of conidiophorc; conidia on
short denticles
Chromelosporium
80
37e Fertile cells somewhat elongated; conidia borne on long pegs or branches
37f
38a Conidia in more or less compact heads; conidiophores simple
39
38b Conidia not in compact heads; conidiophores simple or branched near the apex
41
39a Conidia in dry heads
94
Aspergillus
39b Conidia held in heads of slime
40a Simple diverging sterile arms subtending heads
40b No sterile arms below conidial heads
40
Gliocephalotrichum
Gliocephalis
94
94
4!a Conidia in basipetal chains
42
41 b Conidial chains formed by segmentation of cells or branches of conidiophore
44
MGNIHALES
13
41 c Conidia not catenulate
45
42a Conidiophores usually separate, not in columns or cushions
43
42b Conidiophores and conidia in tall aggregates
Metarrhizium
94
42c Conidiophores and conidia in slimy cushions
Myroihecium
146
43a Conidia phialospores; phialides divergent, loose
Paecihmyces
94
Pemcillium
94
Scopulariopsis
98
43b Conidia phialospores; phialides upright, brushlike
43c Conidia annelospores
44a Arthrospores barrel-shaped, separated by prominent slender cells
44b Arthrospores rod-shaped to globose, separating cells not prominent
Amblyosporium
Oidiodendron
68
68
45a Rough-walled aleuriospores (chlamydospores) present
46
45b Rough-walled aleuriospores absent
48
46a Aleuriospores 1-celled, with attached hyaline cells
46b Aleuriospores
1
-celled,
smooth
walled
Stephanoma
82
Botryoderma
86
Sepedonium
82
46c Aleuriospores 1-celled, rough walled, without attached cells
46d Aleuriospores 2-celled; apical cell large, rough, basal cell small, smooth
47
47a Phialospore state verticillate (like Verticillium)
47b Phialospore state aspergilliform (like Aspergillus)
Mycogone
82
Chlamydomyces
82
48a Conidia produced at or near apex of phialides or branches of conidiophores
49
48b Conidia attached both at apex and side of conidiophore or its branches
57
49a Larger conidiophores (at least) verticillate
50
49b Branches of conidiophores irregular, not verticillate
51
50a Phialospores in mucilaginous clusters
50b Sympodulospores in dry clusters
Verticillium
92
Calcarisporium
102
51a Conidia not aggregated in slime drops
52
51 b Conidia held in heads by slime drops
54
52a Conidia abundant, borne on inflated apical cells
53
52b Conidia single or in small clusters, not on inflated cells
55
53a Conidiophores tall, with one (or few) central axis and several equal,
lateral branches
53b Conidiophores tall, with irregular branches
53c Conidiophores tall, with regular dichotomous branching
53d Conidiophores short, with few branches
54a Conidiophore branches brushlike, similar to Peniciltium
Botryosporium
76
Botrytis
76
Dichobotrys
78
Phymatotrichum
78
Gliocladium
92
14 K E Y TO GENERA
54b Conidiophore branches spreading, not brushlike
Trichoderma
92
55a Conidiophore branches loose, conidia present
56
55b Reproductive structure compacted, globose or pyramidal, bearing globose
cells but no true conidia
Cristulariella
74
56a Saprophytic on leaves
98
56b Saprophytic on wood; conidial state of Hypoxylon
Hansfordia
Nodulosporium
100
57a Fertile portion of conidiophore (or sporogenous cell) zig-zag rachishke
58
57b Fertile portion of conidiophore (or cell) not zig-zag, or rachislike
60
58a Conidiophores simple or verticillately branched
59
58b Conidiophores irregularly branched
59a Conidiophores bulbous at base; parasitic on insects
59b Conidiophores slender, not bulbous; not parasitic on insects
Geniculosporium
Beauveria
100
Tritirachium
100
60a Conidia borne on short denticles
60b Conidia apical on branches, not on denticles
6!a
Conidiophores slender, with slender branches from main axis;
not dichotomous
61b Conidiophores slender to stout; fertile cells somewhat inflated
100
61
Botryoderma
86
Calcarisporium
102
Chromelosporium
80
62a Conidiophores well developed, branched
63
62b Conidiophores mostly simple or with few branches
66
62c Conidiophores none, reduced to cells of stroma
Rhynchosporium
63a Conidia ovoid to oblong
63b Conidia (sympodulospores) obovoid
63c Conidia (phialospores) slender, cylindrical
64a Conidiophore branches restricted to apical region
108
64
Genicularia
Cylindrocladium
Candelabrella
64b Conidiophore branches not restricted to apical region
110
108
110
65
65a Conidia in loose moist clusters
Diplosporium
108
65b Conidia in loose tangled chains
Cladobotryum
108
66a Apical cell of conidium much larger than basal cell
67
66b Conidial cells not differing greatly in size
70
67a Aquatic on submerged leaves
Heliscus
67b Not aquatic
68a Both cells of conidium smooth walled
68b Apical cell of conidium rough walled; basal cell smooth
108
68
Genicularia
110
69
MON1LIALES
69a Microconidial state, if present, similar to Aspergillus
69b Microconidial state, if present, similar to Verticiltium
15
Chlamydomyces
82
Mycogone
82
70a Conidiophores single, not clustered; mostly saprophytic
71
70b Conidiophores clustered; parasitic on leaves
73
71a Conidia borne singly on short pegs or denticles at or near apex of comdiophore
72
71 b Conidia borne successively at pointed apex of comdiophore
72a Conidiophores tall, slender; conidia obovate to oblong
Trichothecium
108
Arthrobotrys
110
72b Conidiophores short; conidia cylindrical to clavate
Dactylaria
110
73a Conidia cylindrical, often in short chains
Ramularia
110
73b Conidia ovoid to oblong, not catenulate
Didymaria
110
74a Conidia long, cylindrical, often bent or curved; aquatic
75
74b Conidia shorter or not cylindrical; aquatic or not
76
75a Conidiophores branched near apex; conidia 1 - or few-celled
75b Conidiophores simple; conidia single, apical
Flagelhspora
138
Anguillospora
140
76a Conidia 2- to several-celled, phragmosporous, not branched
77
76b Conidia branched, staurosporous
84
77a Causing dermatomycoses of man or animals
78
77b Saprophytic or parasitic on plants
79
78a Macroconidia clavate, rounded at apex
Trichophyton
116
78b Macroconidia spindle-shaped to ellipsoid
Microsporum
116
Fusarium
130
79a Macroconidia typically curved, pointed (canoe-shaped),
small conidia usually also present
79b Other than in macroconidia, not canoe-shaped
80
80a Conidiophores short, mostly simple or with few branches
81
80b Conidiophores tall, simple or branched
85
81 a Conidia cylindrical, mostly straight, or slightly curved
82
81 b Conidia ellipsoid or long attenuated
83
82a Conidia catenulate; conidiophores clustered
Septocylindrium
128
82b Conidia not catenulate (sympodulospores); conidiophores single
Scolecobasidium
114
Cylindrocarpon
130
Fusoma
116
82c Conidia not catenulate (phialospores); conidiophores single
83a Conidia ellipsoid, rounded at apex
83b Conidia cylindrical to filiform
84
16
KEY TO GENERA
84a Conidium with apical appendage
Spermospora
128
84b Conidia without appendages
Cercosporella
128
85a Conidiophores mostly simple, seldom branched
86
85b Conidiophores typically branched
95
86a Parasitic on grasses
Pyricularia
86b Saprophytic or parasitic on nematodes
87a Middle cell of conidium greatly enlarged
128
87
Monacrosporium
87b Middle cell only slightly or not at all enlarged
118
88
88a Conidia ovoid to clavate to cylindrical
Dactylaria
110
88b Conidia fusiform to cylindrical
Dactylella
128
89a Branches of conidiophore (phialides) verticillate
Dactylium
130
Cylindrocladium
108
89b Conidiophores terminating in penicilliate branches
90a True staurosporous conidia formed
91
90b No true conidia known; "conidial" branches forming a well defined globose or conical
structure, similar to a loosly formed sclerotium
Cristulariella
74
91 a Conidiophores reduced, not evident
Thallospora
142
91b Conidiophores distinct, well formed, length variable
92
92a Conidial branches not greatly divergent
93
92b Conidial branches widely divergent
94
93a Conidial branches typically 2-pronged
Dicranidion
138
93b Conidial branches typically 3-pronged
Tridentaria
140
94a Central cell of conidium much enlarged
95
94b Central cell of conidium not enlarged
97
95a Conidia pyriform or clavate, with 3 slender branches
Clavariopsis
140
95b Conidia with central globose cell and 4 to 5 slender branches
Actinospora
140
95c Conidia with 3 to 4 broad cells in main axis and 2 to 4 slender appendages
96a Conidial appendages attenuated, pointed
96b Conidial appendages not distinctly attenuated
96
Ingoldia
138
CuHcidospora
140
97a Conidia borne on phialides or phialide-Iike branches of the conidiophore
98
97b Conidia borne otherwise
99
98a Conidium with elongated axis and 2 lateral branches arising side by side
Alatospora
142
98b Conidium with 4 divergent branches arising near base of conidium
Lemonniera
138
MONILIALES
99a Conidial branches formed one at a time
99b Conidial branches formed simultaneously
100
103
100a Conidial branches 4 or more
100b Conidial branches 3 or less
101a Main axis of conidium broader than branches
101b Main axis of conidium about the same width as branches
17
101
104
Tetracladium
140
102
102a Number of branches variable mostly arising from one side
of main axis
102b Conidial branches dendroid, not limited to one side of main axis
Varicosporium
Dendrospora
138
140
103a Conidial branches arising from different levels
103b Conidial branches arising from base of central axis
Tricladiutn
Triscelophorus
138
138
Articulospora
Tetrachaetum
142
140
104a Conidial branches arising from near apex of main axis
104b Two conidial branches arising about midway of slender axis
DEMATIACEAE
105a
105b
105c
105d
Conidia typically 1-celled
Conidia typically 2-celled
Conidia typically 3- or more-ceiled phragmospores
Conidia typically 3- or more-celleddictyospores
106
145
156
184
106a Conidiophores absent or, if present, often poorly developed, consisting of
1 to few cells
106b Conidiophores mostly tall and well developed, cells distinct from conidia,
simple or branched
107a Blastospores borne directly on sides of mycelium, budding freely
107b Dark globose cells of the mycelium breaking up to form 1- to several-celled
segments; conidiophorelike structures may also be present
107c Conidia appearing as blastospores, not budding, broadly ovoid to lenticular,
with a hyaline slit on one side
107d Conidia other than blastospores, not normally budding; conidiophore cells
usually distinct but short
108a Conidiophores extending slightly in length; conidia formed as meristem
arthrospores
108b Conidia other than arthrospores
107
122
Aureobasidium
70
Torula
74
Papularia
82
108
Wailemia
92
109
109a Conidia formed as aleuriospores
109b Conidia formed as phialospores, sympodulospores, or annellospores
110
114
110a Conidia globose
Ill
18
KEY TO GENERA
I !0b Conidia ellipsoid or pointed at apex
II la
112
Conidia black and shiny, borne singly, apically on a special flat
hyaline cell
11 lb Conidia apical, brown, not on a flat special cell
11 lc
Conidiophore reduced to one cell; conidia single, with a hyaline germ pore
on one side
11 Id Conidia single on short branch; no germ pore evident;
dark setae present
112a Conidia rough-walled, pointed at apex
Nigrospora
82
Humicola
84
Gilmaniella
84
Botryothchwn
84
Echinobotryum
84
112b Conidia smooth-walled, ellipsoid
113
113a Conidiophores short, hyaline, repeatedly branched
Wardomyces
84
II 3b Conidiophore branches few; conidia borne on slender stalks
Asteromyces
84
Mammaria
84
113c
Conidiophore branches few; conidia sessile; germ slit evident on one side
I I4a Conidiophores separate; sympodulospores hyaline, somewhat curved
114b Conidiophores compacted into stromalike layers; sympodulospores
dark, pointed at apex
114c
1
Conidiophores compacted into stromalike layer; annellospores dark,
pointed at apex
1
4
d
Conidia
formed
as
Idriella
102
Fusicladium
112
Spilocaea
106
phialospores
115
115a
Conidia slightly curved, narrowly ellipsoid; simple curved setae present.. Circinotrichum
90
U5b
Conidia slightly curved, narrowly ellipsoid; branched, curved setae present... Gyrothrix
90
115c
Conidia ovoid to rod-shaped; no setae present
116a
Conidia with slender appendage at each end; conidiophore branched
116
116b Conidia with slender appendage at each end; conidiophore unbranched
1
117a
1
6
c
Conidia
without
Conidia ovoid, hyaline to dark, often in chains, not in heads
Menispora
88
Codinae
88
appendage
Monilochaetes
117b Conidia mostly ovoid, in small slimy heads, not catenulate
117
86
118
1 1 7 c Conidia rod-shaped, with blunt ends, little or no slime, often present in long chains 1 1 9
118a
Phialides often with enlarged base with flaring collar; conidia hyaline
Phialophora
88
118b Phialides slender, collar not noticeably flared; conidia hyaline
Chloridium
88
118c
Gliomastix
86
Phialides slender, collar not flaring; conidia dark
1
1
1
1
9
9
a
b
Dark
No
chlamydospores
dark
chlamydospores
120a Chlamydospores nearly globose, mostly single
120b Chlamydospores formed in a row, breaking up into single cells
present
present
120
121
Chalaropsis
90
Thielaviopsis
92
MON1LIALES
121a Dark, simple, pointed setae present
19
Chaetochalara
90
Chalara
90
121b No setae present
122a Conidia, sympodulospores, formed on new growing points on conidiophores
123
122b Conidia formed in other ways, not sympodulospores
130
123a Conidiophores simple
124
123b Conidiophores branched
125
124a Apex of conidiophores enlarged, rounded, bearing numerous hyaline conidia on short
sporogenous cells
Basidiobotrys
100
I24b Conidiophores pointed at apex; conidia hyaline, ovoid, attached at tip and sides
of conidiophores
Rhinocladiella
104
124c Conidia obconic, pointed at apex, dark
104
Beltrania
125a Conidiophore branches or phialides borne on side of conidiophore
126
125b Branches of conidiophore confined to area near apex
127
125c Branches of conidiophores irregular
128
126a Branches in whorls; conidia somewhat curved
126b Conidia in unbranched chains, rod-shaped
Mid. Branches loosely arranged; conidia dark, without slime
Selenosporella
102
Sympodiella
104
Periconiella
104
127b Conidiophores repeatedly branched; branches compact; conidia
hyaline in slime heads
Verticicladiella
104
I27c Conidiophores repeatedly branched near apex; conidia not borne
in slime heads
,
,
Verticicladium
104
128a Conidia borne on somewhat enlarged branch tips
Nodulosporium
100
128b Conidia borne on elongated fertile portion of conidiophore branches
129
129a Conidiophores with main axis and numerous lateral branches; conidia dark... Conoplea
102
129b Main axis of conidiophore not evident; conidia hyaline, symmetric
100
129c
Main axis of conidiophores not evident; conidia dark, asymmetric
Geniculosporium
Virgaria
100
130a Conidia blastospores or appearing to be produced as such
131
130b Other than in conidia, not blastospores
136
13la
132
Conidia hyaline
13Jb Conidia dark
132a Dark special cells (falcs) bearing sporogenous cells
132b Without dark falcs on conidiophores
133
Zygosporium
72
Haplographium
80
133a Dark pointed setae present
134
133b Without dark setae
135
20
KEY TO GENERA
134a Conidiophore with enlarged rounded apical cell
134b Conidiophores with slender apical cells
135a Conidia borne on apical inflated cells
135b Conidia borne on inflated cells at apex and intercalary cells
of conidiophores
135c Conidia borne in acropetal chains of variable size and with scars
Lacellinopsis
Lacellina
78
78
Periconia
74
Gonatobotryutn
Cladosporium
78
106
136a Conidia (phialophores) borne at apex of conidiophores
136b Conidia not phialospores
137
143
137a Conidiophores simple, unbranched
138
137b Conidiophores branched
139
138a Conidia in moist (slimy) heads
Stachybotrys
88
138b Conidia in dry chains; apex of conidiophores not enlarged
138c Conidia in dry chains; apex of conidiophores enlarged, rounded
Memnoniella
Aspergillus
88
94
139a Branches of conidiophores lateral; conidiophores with sterile apex
139b Conidiophore branches clustered at or near apex, without sterile apex
140
141
140a Conidia ovoid; phialides dark
140b Conidia oblong, cylindrical; phialides hyaline
Gonytrichum
Chaetopsina
98
96
141a Conidiophores hyaline; few conidia large, dark, lemon-shaped
14Tb Conidiophores dark; other than in conidia
Phialomyces
94
142
142a Conidia rod-shaped, elongate with blunt ends, catenulate
Phialocephala
96
142b Conidia elongate fusoid, ends pointed
142c Conidia ovoid, not catenulate
Thysanophora
Stachylidium
96
92
Arthrinium
74
144
Leptographium
98
Microclavia
Staphylotrichum
80
80
143a Conidia formed as meristem arthrospores; conidiophores with
thick dark septa
143b Conidia and conidiophores not as above
144a Conidia annellospores, conidia in slime heads
144b Conidia aleuriospores; conidiophores simple with two dark
conidia at apex
144c Conidia aleuriospores; conidiophores irregularly branched
145a Conidia catenulate
145b Conidia not catenulate
146
147
146a Conidiophores simple, tall, segmenting into rod-shaped arthrospores
146b Conidia formed in acropetalous unbranched chains (blastospores)
Ampuliferina
Bispora
106
106
146c Conidia formed in branched chains, single-celled conidia also present
(blasto
spores)
146d Conidia formed as rows of dark chlamydospores (aleuriospores)
Cladosporium
Trichocladium
106
118
MON1LIALES
146e
Conidia formed as lateral branches through pores (porospores)
147a
Conidiophores clustered on surface or breaking out from stroma
Diplococcium
114
148
I47b Other than in conidiophores, mostly single
153
148a Conidiophores wavy, in loose clusters on surface of leaves
Polythrincium
148b Conidiophores not wavy, arising from within leaf
149a
21
112
149
Conidia on stroma, with apical, rounded cells
Asperisporium
112
149b Conidia on stroma, apical cell pointed
150
150a
151
Conidiophores very short, on flat stroma
150b Conidiophores tall
151a
152
Conidia annellospores
151b Conidia sympodulospores
152a Conidiophores branched
152b Conidiophores unbranched
Spilocaea
106
Fusicladium
112
Passalora
112
Scolecotrichum
112
} 53a Conidiophores simple
154
153b Conidiophores branched
155
154a Conidiophores short, stout, composed usually of 1 or 2 cells
Scolecobasidium
114
Cordana
112
Spadicoides
114
Pseudobotrytis
106
Chaeiopsis
96
Balanium
106
Sporoschisma
130
154b Conidiophores tall, slender; conidia clustered at apex
154c
Conidiophores tall, slender; conidia formed from lateral pores
155a
Branches restricted to apical area where radiating
sporogenous cells form
155b Several lateral branches of conidiophores end in sterile apical point
155c
Conidiophore branches short, irregular, on short conidiophore
156a
Conidia endogenous; conidiophore with a single swollen, terminal
phialide
156b Conidia exogenous; other than in conidiophores
157
157a
158
Conidiophores typically branched
157b Conidiophores typically simple, rarely branched
158a
Conidial chains basipetal, conidia not truly end to end
158b Conidia] chains acropetal, conidia truly end to end
159a Conidia slender, much longer than wide
i 59b
Conidia much broader, usually length not 3 to 4 times width
160a
Conidia with very thick wall, formed by expansion of apical conidiophore
cells
159
Fusariella
Septonema
Cladosporiella
130
116
92
160
Murogenella
114
22
KEY TO GENERA
160b Conidia formed distinct from conidiophore cells
161
161a Conidiophores clustered or fascicled
162
161b Conidiophorcs single, separate
165
162a Conidiophores in tall fascicles
162b Conidiophores in small, compact cushion-shaped structures
Phragmocephala
118
Cercosporidium
122
162c Conidiophores clustered at base; upper portion divergent
163
163a Conidiophores short, bearing annellospores
Stigmina
163b Conidiophores tall, showing sympodial growth
164a Conidia dark, oblong
164b Conidia long, slender, hyaline
120
164
Heterosporium
122
Cercospora
128
165a Conidiophores short, consisting of 1 to few cells, or absent
166
165b Conidiophores tall, typically consisting of several cells
172
I66a Conidia of two kinds, dark phragmospores, and lighter scolecospores
167
166b Dark phragmospores only
168
167a Conidia in acropetalous chains
167b Conidia not in chains
168a Conidia botryoblastospores
168b Conidia annellospores
Pseudotorula
116
Dwayabeeja
116
Cephaliophora
116
Deightoniella
118
I68c Conidia aleuriospores
169
169a Conidia much longer than broad
170
169b Conidia not much longer than broad
171
170a Conidia long-cylindrical, separating cell at tip of conidiophore
evident
Camposporium
116
170b Conidia somewhat broader at middle, apical cell attenuated or hooked; no separating
cell
Ceratophorum
118
170c Conidia long, broadest at middle, narrowed toward each end; no separating
cell
Clasiei'o.sporium
118
171a Conidia rounded, nearly globose (may appear as a chain of
chlamydospores)
Trichocladium
118
Pithoniyces
132
I7Ib Conidia broadly ellipsoid, phragmospores and dictyospores may be
present
172a Conidiophores determinate, not elongating with successive conidial formation
173
172b Conidiophorcs indeterminate, elongating after each successive conidial formation
174
173a Conidia produced through pores at sides of conidiophores
114
Spadicoidcs
MONILIALES
173b Conidia apical, single, several-celled, parasitic on leaves
23
Corynespora
120
173c Conidia apical, several-celled, saprophytic
Sporidesmium
120
173d Conidia apical, 3- to 5-celled, saprophytic
Endophragmia
118
174a Conidiophores proliferating at apex, leaving annulate scars
175
174b Conidiophores elongating sympodially
176
175a Conidia narrowed or pointed at apex
'.
175b Conidia mostly ovoid with rounded apex
176a Conidia with 1 to 4 slender hyaline appendages
Annellophora
118
Endophragmia
118
Pleiochaeta
128
176b Conidia without appendages
177
177a Conidia in apical clusters or heads
178
177b Conidia not confined to apex of conidiophore
181
178a Conidia borne on slender pedicels
Brachysporium
178b Conidia not borne on slender pedicels
179
179a Conidia hyaline
Pleurothecium
179b Conidia dark
180a
126
126
180
Conidia borne on short hyaline projection through apex of
conidiophore
Cacumisporium
124
180b Conidia borne near apex but not on special cell of conidiophore
Pleurographium
126
181a Conidia distinctly narrowed at both ends
182
181b Conidia straight or only slightly narrowed, ends rounded
183
182a Conidia porospores, borne in whorls on cells of straight, simple
conidiophores
Helminthosporium
182b Conidia sympodulospores
183a Conidia catenulate
183b Conidia not catenulate, usually 4-celled, bent by enlargement of one of
middle cells
183c
Conidia not catenulate, several-celled, straight or slightly
curved
124
Nakataea
128
Dendryphion
124
Curvulana
122
Drechslera, Bipolaris
122,126
184a Conidia catenulate
185
184b Conidia not catenulate
186
185a Conidial development basipetal
Coniosporium
134
185b Conidial development acropetal
Alternaria
132
186a Conidium with large swollen apical cell
Acrospeira
132
186b Apical cell of conidium not distinctly swollen
187
24
KEY TO GENERA
187a Conidiophores well developed, usually longer than conidia
188
187b Conidiophores poorly developed or none
192
188a Conidia apical, single
189
188b Conidia appearing apical and lateral due to growth of conidiophore
192
189a Conidia sharply attenuated at apex
Alternaria
I89b Conidia somewhat narrower or not at apex
190a
190
Conidia subglobose, ovoid, or broadly ellipsoid
190b Conidia elongate, straight to flexuous
191a
Conidia with 4 cells, cross-shaped
Conidia several-celled, narrowly elliptical, ends pointed
I92a
Conidiophores single, not clustered
Stemphylium
132
Sirosporium
134
Dictyoarthrmium
191 b Conidia several celled, not cross-shaped, broadly elliptical, ends rounded
191c
Ulocladium
Dactylosporium
134
132
134
193
192b Conidiophores clustered, often into a loose sporodochiumlike structure
193a On living leaves, parasitic
132
194
Stigmella
134
193b Saprophytic in soil or humus
Pithomyces
132
194a Conidia globose to subglobose
Epicoccum
150
Berkleasmium
134
194b Conidia very large, oblong to obovoid
195a Branches of conidium upright, parallel, or slightly divergent
196
195b Branches of conidium upright or lateral, widely divergent
197
196a Conidial branches connected
Dictyosponum
144
196b Conidial branches separate; conidia catenulate or
produced successively
Ceratosporella
144
196c Conidial branches separate; conidia apical, single
Speiropsis
142
1 9 7 'a Conidiophores present, distinct, length variable
198
197b Conidiophores absent or reduced to short pegs
199
198a Conidia (aleuriospores) apical, single
Triposporium
144
198b Conidia (sympodulospores) apical on new sympodial growing points
Diplodadiella
142
199a Conidia with 2 to 3 straight or curved upright horns
199b Conidia with 3 to 4 basal cells, each attenuated above
199c
Tetrapha
142
Tripospermum
142
Hirudinaria
144
Ceratosporium
144
Conidiophores united into sporodochia (Tuberculanaceae). Sporodochia may be poorly
formed in culture; some species may be similar in appearance to Melanconiales
202
Conidia with 4 to 5 divergent arms at wide angles
200a Parasitic on leaves
200b Saprophytic, mostly on wood
201a
200
MONIL1ALES
201b Conidiophores united into synnemata (Stilbaceae); free conidiophores often also
present
25
225
TUBERCULARIACEAE
202a Conidia I-celled, hyaline or dark
202b Conidia 2-ceIIed, dark
203
Pucciniopsis
148
202c Conidia typically more than 2-celled, hyaline or dark
215
203a Conidia hyaline or brightly colored
204
203b Conidia or sporodochia with dark pigment
213
204a Sporodochia stromalike, spreading, on developing grain
Sphacelia
204b Sporodochia cushion-shaped to discoid, not on grain
205a Sporodochia with prominent setae or sterile hairs
205
Myrothecium
205b Sporodochia without setae or sterile hairs
206a Sporodochia developing in rust pustules on plants
148
146
206
Tuberculina
148
206b Sporodochia superficial, not in rust pustules
207
207a Conidia catenulate or in pillarlike masses
208
207b Conidia not catenulate or in pillarlike structures
210
208a Conidia hyaline or yellowish in mass
Sphaerosporium
208b Conidia usually greenish in mass
146
209
209a Conidiophores and conidia in tall columnar aggregates
Metarrhizium
94
209b Conidiophores and conidia in slimy masses or loose columns
Myrothecium
146
Hymenella
146
210a Sporodochia discoid, flattened
210b Sporodochia cushion-shaped to hemispherical
21 la Conidiophores verticillately branched
211
Dendrodochium
21 lb Conidiophore branching irregular
212a On wood or bark
212b On leaves
2 J 3a On scale insects
212
Tubercularia
146
Illosporium
146
Aegerita
150
213b Not on scale insects
214a Sporodochia erumpent from leaves
214b Sporodochia superficial on bark or wood
215a Conidia hyaline or brightly colored
146
214
Hadrotrichum
146
Strumella
146
216
26
K E Y TO GENERA
215b Conidia with dark pigment
218
216a Conidia large, cylindrical to ellipsoid; yellowish in mass
Bactridium
216b Conidia slender, hyaline in mass
217
217a Macroconidia canoe-shaped; I-celled conidia also may be present
217b Conidia curved but not canoe-shaped
148
•
Fusarium
130
Ramulispora
148
218a Conidia branched or lobed
219
2I8b Conidia not branched or lobed
220
219a Conidia with short, compact upright branches
219b Conidia 4-lobed, cross-shaped
Cheiromyces
150
Spegazzinia
150
220a Conidia (dictyospores) muriform
221
220b Conidia (phragmospores) 3- to several-celled
223
221a Conidia globose to subglobose
221 b Conidia broadly cylindrical to ovoid, very large
Epicoccum
150
Berkleasmium
134
222a Sporodochia without setae
222b Sporodochia with dark setae
223a Conidiophores arising from special enlarged cells
223b Conidiophores not arising from special enlarged cells
223
Excipularia
148
Camptomeris
150
Bactrodesmium
150
STILBACEAE
225a Not parasitic (or saprophytic) on insects or spiders
226
225b Parasitic (and probably saprophytic) on insects or spiders
243
226a Conidia 1 -celled
227
226b Conidia 2- or more-celled
236
227a Conidia hyaline
228
227b Conidia dark
233
228a Comdiogenous portion of synnemata located or near apex in more or less globose
head
229
228b Conidiogenous portion of synnemata elongate to cylindrical
232
229a Head composed of loosely arranged conidiogenous hyphae
229b Head composed of compact conidiogenous hyphae
230
231
MONILIALES
230a Head with numerous radiating sterile hyphae
Heterocephalum
152
Tharoopama
156
Stilbum
152
230b Radiating sterile hyphae not present
231a Stalks of synnemata hyaline
231b Stalks of synnemata dark
Graphium, Peso turn 152
232a Synnema with tall, central seta
232b Central seta absent
27
Menisporopsis
'.
Harpographium
152 ,
156
233a Conidiogenous portion of synnemata confined to compact apical region
234
233b Conidiogenous region cylindrical
235
234a Synnemata funnel-shaped with narrow base
Endocalyx
234b Synnema slender, uniform, with globose head
152
Briosia . 152
235a Sterile hairs or setae present among conidiophores
235b Sterile hairs not present
Trichurus
156
Doratomyees
154
236a Conidia 2-celled
237
236b Conidia 3- or more-celled
238
237a Synnemata and conidia hyaline
237b Synnemata and conidia dark
Didymostilbe
154
Didymobotryum
156
238a Conidiogenous portion of synnema only at or near apex
239
238b Conidiogenous portion of synnema longer, cylindrical
242
239a Conidial portion in compact, more or less globose heads
240
239b Conidial portion with loose conidiophores, not so compact
241
240a Conidia with cross walls only (phragmosphores)
Arthrobotryum
154
240b Conidia with both cross and oblique walls (dictyospores)
Sclerographium
158
241a Conidial branches at apex, short; conidia pointed at apex
Acarocybe
158
hariopsis
154
241c Conidiophores compact at base, diverging near apex, conidia rounded at
ends
Dendrographium
154
242a Conidia hyaline
Arthrosporium
154
Podosporium
154
242c Conidia dark, borne on sympodial conidiophore
Spiropes
158
243a Phialides in globose or wedge-shaped heads
Gibellula
160
241 b Conidiophores in a loose fascicle, not branched; conidia pointed at apex
242b Conidia dark, borne singly at apex of conidiophore
243b Phialides not in definite heads
244
28
KEY TO GENERA
244a Phialides short, in compact layer
245
244b Phialides usually large, not in compact layer
246
245a Synnemata cylindrical; phialides obtuse at apex
Hymenostilbe
158
Insecticola
158
245b Synnemata clavate; phialides pointed at apex
245c Synnemata cylindrical to attenuated; phialides pointed
Akanthomyces
246a Phialides elongate, slender; conidia covered with slime
247
246b Phialides not elongate; conidia dry
247a Phialides enlarged at base; conidia not in heads
247b Phialides not enlarged at base; conidia in heads
158
Isaria
156
Hirsutella
160
Synnematium
160
SPHAEROPSIDALES
la Conidia globose to oblong or ellipsoid, not filiform
2
lb Conidia filiform, at least several times longer than wide, I- to several-celled
(scolecosporous)
62
2a Conidia 1 -celled
3
2b Conidia typically 2-cclled
45
2c Conidia typically 3- to several-celled
52
3a Conidia hyaline, or sometimes brightly pigmented in mass
4
3b Conidia with dark pigment, evident at least in mass
40
4a Pycnidia complete, or with well developed base
5
4b Pycnidia not complete, with only the upper portion well developed
37
5a Pycnidia separate, not in stromata
6
5b Pycnidia in stromata, frequently evident only by pycnidial cavities
6a Pycnidia mostly ovoid; parasitic on powdery mildews
29
Ampelomyces
166
6b Pycnidia with long beak or neck; not parasitic on powdery mildews
7
6c Pycnidial beak short or absent; not parasitic on powdery mildews
9
7a Pycnidial walls dark
Sphaeronaema
7b Pycnidial wall hyaline or light colored
8a Pycnidia] wall composed of long parallel hyphae
168
8
Hyalopycnis
168
8b Pycnidial wall composed of short, angled pseudoparenchymetous cells .. Eleutheromyces
168
9a Pycnidia breaking open irregularly, without a distinct ostiole
10
9b Pycnidia opening by distinct ostioles
18
10a Pycnidia with dark setae
11
SPHAEROPSIDALES
10b Pycnidia without dark setae
29
12
I la Conidia with a slender appendage at each end
II b Conidia without appendages
Dinemasporium
172
A merosporium
172
I2a Pycnidia superficial, on surface of substratum
13
12b Pycnidia at least partially within substratum
14
13a Pycnidia soft, leathery, subglobose, not on subiculum
13b Pycnidia hard, irregular, on subiculum
Cannula
172
Chaetophoma
164
Sclerotiopsis
166
14a Pycnidia large, resembling sclerotia; conidia ellipsoid
14b Pycnidia not resembling sclerotia; conidia ovoid to ellipsoid
15
15a Pycnidia fleshy, bright colored when fresh
Hainesia
15b Pycnidia hard, dark
174
16
16a Pycnidia subcortical, on woody twigs
Dothichiza
16b Pycnidia subepidermal, on fleshy tissue or leaves
172
17
17a Pycnidia discoid, dehiscing radiately
Sporonema
172
17b Pycnidia globose, opening at apex
Plenodomus
162
18a Pycnidia on subiculum of radiating hyphae
Asteromella
164
18b Pycnidia not on subiculum
,
19
19a Conidia of 2 kinds: short-ovoid and long-curved or bent
Phomopsis
19b Conidia all of one kind
164
20
20a Conidia typically lunate
Seienophoma
20b Conidia ovoid; dark dictyosporous chlamydosphores present
Peyronellaea
162
164
20c Conidia globose to ellipsoid, straight or slightly curved; without dictyosporous
chlamydospores
21
21 a Conidiophores branched
22
21
b
Conidiophores
22a Conidia with apical appendages
22b Conidia without appendages
simple
23
Eleutheromycella
168
Dendrophoma
162
23a Conidia with hyaline membraneous appendages
24
23b Conidia without appendages
25
24a Conidial appendage apical, obconical
24b Conidial appendage slender, turned back
Neottiospora
166
Anthasthoopa
174
25a Pycnidia superficial on natural substratum
26
25b Pycnidia embedded in natural substratum
27
30
K E Y TO GENERA
26a Pycnidia tapering below into a short stalk
26b Pycnidia not tapering at base
27a Conidia longer than 15 microns
Rhizosphaera
164
Aposphaeria
162
Macrophoma
164
27b Conidia 15 microns or shorter
28
28a Setae present on pycnidia
28b No setae present on pycnidia
Pyrenochaeta
162
Phyllosticta, Phoma
162
29a Conidia having one or more apical appendages
30
29b Conidia without appendages
3J
30a Conidia with an apical and a basal appendage
30b Conidia with short branched appendages at both ends
31a Stromata superficial, soft, brightly colored
Shanoria
172
Dilophospora
166
Aschersonia
174
31b Stromata subepidermal or subcortical, dark
32
32a Conidia fusoid, ends pointed
Fusicoccum
170
32b Conidia not fusoid, ends rounded
33
33a Conidiophores tall, slender, septate
34
33b Conidiophores short, seldom septate
35
34a Conidia borne apically only on conidiophores
*
34b Conidia borne apically and laterally on conidiophore
35a Conidia ovoid to broadly ellipsoid; pycnidial cavaties globose
Rabenhorstia
170
Pleurostromella
170
Dothiorella
166
35b Conidia narrow, ovoid to filiform; pycnidial cavities irregular
36a Conidia mostly filiform, bent or curved
36b Conidia short, curved
36c Conidia short, not curved
36
Cytosporina
166
Cytospora
170
Cytosporella
170
37a Pycnidia shield-shaped, with or without ostiole
38
37b Pycnidia flat, opening wide at maturity
39
38a Pycnidia borne on a short stalk or column
38b Pycnidia without stalk or column
39a Stroma present
Actinopelte
174
Leptothyrium
174
Melasmia
174
39b Stroma absent
Leptostroma
176
40a Pycnidia with prominent dark bristles (setae)
Chaetomella
176
40b Pycnidia without bristles (setae)
41a Pycnidia light colored; conidiophores long, filiform
41
Harknessia
176
SPHAEROPSIDALES
41 b Pycnidia dark; conidiophores short
42a Parasitic on powdery mildews
42
Ampelomyces
42b Not parasitic on powdery mildews
43a Stromata embedded in bark or wood
44b Conidia small, globose to ovoid; without dark chlamydospores
44c Conidia small, ovoid; dark dictyosporous chlamydospores present
166
43
Haplosporetta
43b Pycnidia not in stromata
44a Conidia large, ovoid to elongate
31
178
44
Sphaeropsis
176
Coniothyrium
176
Peyronellaea
164
45a Conidia hyaline
46
45b Conidia with distinct dark pigment
51
46a Pycnidia in rust pustules; parasitic on rusts
Darluca
178
46b Not parasitic on rusts
47
47a Conidia without appendages
48
47b Conidia with appendages
50
48a Pycnidia in necrotic spots on leaves, etc
Ascochyta
48b Pycnidia not in necrotic spots
49a Pycnidia with distinct beaks
49b Pycnidia without distinct beaks
50a Conidia with an apical awl-shaped unbranched appendage
50b Conidia with 3 to 4 hyaline appendages at one end
51a Pycnidia separate, not in stroma
51 b Pycnidia clustered in stroma
178
49
Rhynchophoma
178
Diplodina
178
Kellermannia
178
Robillarda
178
Diplodia
180
Botryodipiodia
180
52-d Conidia with transverse septa only (phragmosporous)
53
52b Conidia dictyosporous or staurosporous
59
53a Conidia with apical appendages
54
53b Conidia without appendages
55
54a Pycnidia flattened; conidia with 1 appendage at each end
Discosia
182
54b Pycnidia globose; conidia with 3 to 4 appendages
Bartilinia
182
55a Pycnidia brightly colored with cushionlike stroma
Aschersonia
174
55b Pycnidia brown or black, without stroma
56
55c
58
Pycnidia dark, in stroma
56a Pycnidia with dark spines near ostiole; conidia hyaline
Aristatoma
180
32
KEY TO GENERA
56b Pycnidia without spines; conidia hyaline
Stagonospora
56c Pycnidia without spines; conidia dark when mature
180
57
57a Conidia single on conidiophores
Hendersonula
180
57b Conidia grouped at apex of conidiophores
Prosthemium
186
58a Conidia dark
Hendersonia
184
58b Conidia hyaline
Dothistroma
180
59a Conidia dictyosporous, globose to ellipsoid
60
59b Conidia staurosporous
61
60a Pycnidia within a stroma
Dichomera
186
60b Pycnidia not in a stroma
Camarosporium
186
61a Conidia typically with 4 equal radiating arms
Tetranacrium
182
61b Conidia with 3 to 5 equal arms
Prosthemium
186
62a Pycnidia in dark hard stroma
63
62b Pycnidia not in stroma, not gelatinous
64
62c Pycnidia gelatinous or with gelatinous stroma
72
63a Conidia 1 -celled, bent or curved
Cytosporina
166
63b Conidia several-celled, long, cylindrical, straight
Dothistroma
180
64a Pycnidia clavate or with long beak
65
64b Pycnidia globose or flattened
66
65a Conidia hyaline, 1- to 2-celled, filiform-fusoid
65b Conidia dark, several-celled, elongate
Sphaerographium
Cornularia
184
186
66a Pycnidia with distinct ostiolc
67
66b Pycnidia opening by wide mouth or slit
70
67a Conidia pigmented, yellow to light brown
Phaeoseptoria
184
67b Conidia hyaline
68
68a Pycnidia in necrotic spots on leaves, etc
69
68b Pycnidia not in necrotic spots
69a Pycnidia with setae near ostiole
69b Pycnidia without setae
70a Conidia 1 -celled, bent or curved
Rhabdospora
184
Chaetoseptoria
184
Septoria
182
Phlyctaena
186
70b Conidia several-celled, straight or curved
71a Pycnidia flattened, irregular, opening by a slit; conidia not segmenting .. Leptostromella
71
184
SPHAEROPSIDALES
71b Pycnidia globose or cupulate, opening by a wide mouth
72a Conidia I-celled; stroma smutlike, on grass
Phleospura
186
Ephelis
184
72b Conidia several-celled; stroma not smutlike, on wood or bark
73a Stroma elongate, stalked
73
Chondropudium
73b Stroma rounded to irregular, not stalked
186
74
74a Stromal tissue waxy
74b Stromal tissue cartilaginous
33
Mkropera
182
Gelatinosporium
182
MELANCONIALES
la Conidia 1-celled, short, not filiform
2
lb Conidia 2- to several-celled, not filiform, didymosporous or phragmosporous
7
lc Conidia filiform, 1- to several-celled
12
Id Conidia dictyosporous or staurosporous
14
2a Conidia with distinct dark pigment
Melanconium
2b Conidia hyaline
3a Conidia produced laterally on conidiophore
3
Catenophora
3b Conidia produced apically on conidiophore
4a Conidia with apical, hyaline branched appendages
Pestalozziella
6b Stromalike base absent or poorly developed
188
5
Colletotrichum
5b Dark setae absent
6a Conidiophores arising from a stromalike base
188
4
4b Conidia without appendages
5a Dark setae present in acervulus
190
188
6
Sphaceloma
188
Gloeosporium
188
7a Conidia 2-celled, didymospores
8
7b Conidia 3- to several-celled, phragmospores
9
8a Conidia unequally 2-celled, hyaline, without appendages
8b Conidia equally 2-celled, hyaline, with one appendage at each end
8c Conidia typically 2-celled, dark, with basal appendages
9a Conidia hyaline
Marssonina
190
Myculeptodiscus
190
Polynema
192
Sepioglueum
190
9b Conidia with distinct dark pigment
10a All cells of conidia dark
10
Coryneum
194
34 K E Y TO GENERA
10b End cells of conidia hyaline, middle cells dark
11
I la Single beaklike appendages at apex of conidia
Monochaetia
192
Pestalotia
192
Seimatosporium
192
Libertella
190
II b With 2 to 3 appendages at apex of conidia
1 lc Conidia with single apical and basal appendages
12a Saprophytic on wood or bark
12b Parasitic on leaves
13
13a Conidia becoming septate
Cylindrosporium
192
13b Conidia remaining 1-celled
Cryptosporium
190
14a Conidia dictyosporous; some phragmospores may be present
15
14b Conidia straurosporous
16
15a Conidia catenulate
Phragmotrichum
194
15b Conidia not catenulate
Steganosporium
194
Entomosporium
194
Asterosporium
194
16a Conidia hyaline
16b Conidia with distinct dark pigment
MYCELIA STERILIA
la Entire "conidiophore" (except stalk) closely branched, forming a globose
or pyramidal reproductive structure, hyaline, dark sclerotia in culture
and often on leaves
Cristulariella
1 b Conidiophorelike structures absent
2a Sclerotia variable in form, pale to dark brown or black; usually formed
on loosely woven, dark hyphae
2b Sclerotia rounded, variable in size, black; mycelium hyaline
2c Dark brown bulbils or small clusters of compact cells present; hyphae
becoming dark brown
74
2
Rhizoctonia
196
Sclerotium
196
Papulospora
196
SIMPLIFIED K E Y TO SOME
SELECTED COMMON GENERA
la Having characteristics of the Mucorales; coenocytic mycelium and sporangioles that
segment or otherwise appear as conidia
2
I b Having septate mycelium and other characteristics of the imperfect fungi
3
2a Conidiophores (sporangiophores) unbranched except near apex where loose heads of
dark spores are borne
Choanephora
66
2b Conidiophores (sporangiophores) unbranched, bearing an apical cluster of elongate
sporangioles that break up into 1-celled spores
Syncephalastrum
66
2c Conidiophores (sporangiophores) very slender, dichotomously branched, bearing a
cluster of slender sporangioles that segment into short rod-shaped spores.. Piptocephalis
62
3a Conidiophores distinct although short or reduced to pegs in some genera; conidia
typically I-celled, occasionally 2-celled
4
3b Conidiophores distinct or reduced to pegs; conidia typically and predominately with 2
or more cells
35
3c Conidiophores indefinite or absent; conidia rod-shaped with truncate ends, formed by
fragmentation of the mycelium
Geotrichum
68
3d No true conidiophores or conidia present; reproduction by sclerotia or
similar structures
53
,
4a Conidiophores contained within a pycnidium
5
4b Conidiophores compacted into an acervulus or sporodochium in nature, but may be
evident as loosely arranged structure in culture
9
4c Conidiophore stalks compacted into synnemata
12
4d Conidiophores separate, not tightly clustered in any manner
*
15
5a Pycnidia separate, not in a stroma
6
5b Pycnidia embedded in a stroma
8
6a Conidia relatively large, with dark pigment
Sphaeropsis
6b Conidia small, hyaline, no pigment present
176
7
7a Conidiophores with a few upright branches
7b Conidiophores short, simple, unbranched
8a Pycnidia formed as irregular cavities in a stroma; conidia small
8b Pycnidia rounded, regular; conidia large
9a Conidia held together in moist, slimy masses
35
Dendrophoma
162
Phoma or Phyllosticta
162
Cytospora
170
Dothiorella
166
10
36 SIMPLIFIED K E Y TO SOME S E L E C T E D C O M M O N GENERA
9b Conidia dry, without slime
11
10a Conidia with dark pigment, more evident in mass
10b Conidia hyaline; dark setae present
Melanconium
190
Colletotrichum
188
10c Conidia hyaline; setae absent
Gloeosporium
I la On leaves, twigs, or fruit; conidia dark, with pointed apex.."
II b On wood or bark; conidia hyaline, ovoid
188,
Spilocaea
106
Tubercularia
146
12a Both stalks or synnemata and conidia hyaline
13
12b Both stalks of synnemata and conidia dark
14
12c Stalks of synnemata dark; conidia hyaline
Graphium, Pesotum
152
Stilbum
152
13a Conidia held in moist, slimy heads
13b Conidia in dry clusters, not slimy
14a Conidial heads rounded, ovoid to subglobose; parasitic on buds of Azalea
or Rhododendron
14b Conidial portion elongated, usually narrowed at apex
and base, saprophytic
15a
Isaria
156
Briosia
152
Doratomyces
Conidiophores branched or bearing a cluster of branches or phialides
near or at the apex
154
16
15b Conidiophores typically simple or only occasionally branched
26
16a Conidia remaining together in chains of two or more
17
16b Conidia not remaining together in chains
22
17a Conidia acropetal, with youngest at the apex of chain
18
17b Conidia basipetal, with the youngest at the base of chain
19
18a Conidia dark, variable in shape, ovoid, lemon-shaped to oblong,
mostly 1 -celled, some may be 2- to 3-celled
1 8b Conidia dark, uniformly globose, and 1 -celled
Cladosporium
106
Perkonia
74
Monilia
72
Aspergillus
94
19b Conidiogenous cells borne on slender branches, not on swollen apex of conidiophore ...
20
20a Conidiogenous cells bearing annulate scars of previous conidia
98
18c Conidia hyaline, uniformly ovoid to short cylindrical
19a Conidiogenous cells (phialides) borne on apex or swollen apex
of conidiophores
Scopulariopsis
20b Annulate scars not present on conidiogenous cells
21 a Conidiogenous cells (phialides) closely arranged in a brushlike head
21 b Conidiogenous cells divergent, not in a close head
22a Conidia in small clusters held together by slime
21
PenicilUum
94
Paecilomyces
94
23
SIMPLIFIED K E Y TO SOME SELECTED C O M M O N GENERA 37
22b Conidia dry, not held in slime
24
23a Conidiophore branches verticillate, often 3 or more branches arise from
the same level
Verticiliium
92
Thchoderma
92
Nociulosporium
100
23b Conidiophore branches irregular, not verticillate
24a
Conidia formed successively at apex of conidiophore, which continues
to elongate
24b Conidia formed in a head on the more or less swollen apex of the conidiophore
25a Apical sporogenous cell of conidiophore or branches slightly
enlarged, globose
25
Botrytis
76
25b Apical conidiogenous portion and branches distinctly enlarged, cylindrical,
or club-shaped
Chromelospohum
80
26a Conidia (chlamydospores, aleuriospores) terminal, single, globose
27
26b Conidia otherwise
28
27a Conidia black, shiny, smooth
27b Conidia with yellow pigment, rough-walled
28a Parasitic on plants, conidial states of powdery mildews
Nigrospora
82
Sepedonium
82
Oidium
68
28b Not conidial states of powdery mildews
29
29a Conidiophores indeterminate, apex elongating as new conidia are produced
30
29b Conidiophores determinate, not elongating as new conidia are produced
31
30a
Conidiogenous portion of conidiophore zig-zag, elongating to appear
rachislike
Beauveria
30b Conidiogenous portion of conidiophore limited, not rachislike
31a Conidia produced simultaneously on swollen apex of conidiophore
100
Sporothrix
98
Oedocephalum
76
31b Conidia produced single or successively at apex of conidiophore or phialide
32
32a Conidia exogenous, ovoid to globose, borne singly or in pairs on a dark hook (falc)
of conidiophore
Zygosporium
72
32b Conidia endogenous, rod-shaped, often catenulate; no falcs present
Chalara
90
32c Conidia ovoid to globose, held together in small apical clusters by slime; falcs absent ...
33
33a Conidiophores or phialides slender, hyaline
94
Cephahsporiwn
33b Conidiophores or phialides slender or somewhat inflated, with some dark pigment
34
34a Conidiophores tall, slender, uniform in width
Chhridium
88
Phialophora
88
34b Conidiophores short or sometimes absent, often somewhat inflated
35a Conidia typically and uniformly 2-celled, seldom with fewer or more cells
36
35b Conidia typically has more than 3 cells, sometimes variable
43
36a Conidia hyaline, no pigment in walls
37
38
SIMPLIFIED K E Y TO SOME S E L E C T E D C O M M O N GENERA
36b Conidia with dark pigment in walls
37a Conidiophores compacted into an acervulus in nature
41
Marssonina
37b Conidiophores separate, not clustered or compacted
190
38
38a Conidiophores branched, with a sterile terminal branch and swollen apex;
conidia long, cylindrical
Cyiindrocladium
108
38b Conidiophores simple; conidia ovoid or ellipsoid
39
39a Conidia borne singly, apical on sympodial growing points
40
39b Conidia produced basipetally in irregular groups, not on sympodial
growing points
40a Conidia ellipsoid-elongate, cells equal
40b Conidia ovoid to elongate, apical cell somewhat larger
41a Conidiophores and conidia borne in a typical pycnidium
41b Conidiophores and conidia in an acervulus or a stroma in nature
Trichothecium
108
Dactylaria
110
Arthrobotrys
110
Diplodia
180
Spilocaea
106
41c Conidiophores separate or in loose clusters
42a Conidiophores slender, conidia in short acropetalous chains
42b Conidiophores rather stout, zig-zag in appearance;
conidia apical, not in chains
43a Conidia spiral or in coil
42
Bispora
106
Polyihrincium
112
Helicomyces
136
43b Conidia phragmosporous, with cross but not oblique walls
44
43c Conidia dictyosporous, with both cross and oblique walls
52
44a Conidia with slender appendages, at least at apex
Pestalotia
192
44b Conidia without appendages
45
45a Conidia dark
46
45b Conidia hyaline
51
46a Conidia borne in acervuli in bark
Coryneum
46b Conidia not borne in acervuli
47a Conidia in acropetalous chains; some conidia with 1 or 2 cells
47
Cladosporium
47b Conidia single, not in chains
48a Conidiophores with several upright branches
Dendryphiopsis
50b Conidia, with one median cell larger than others
120
49
Helminthusporium
49b Conidia borne apically on new sympodial growing points
50a Conidia straight or slightly curved; cells nearly equal
106
48
48b Conidiophores simple, without branches
49a Conidia produced through pores on sides of conidiophores
194
124
50
Hipolaris
Curvuhria
126
122
SIMPLIFIED K E Y TO SOME SELECTED C O M M O N GENERA 39
51a Conidiophores simple, clustered, dark; conidia long, attenuated
51b Conidiophores hyaline, branched; conidia long, cylindrical
Cercospora
Cylindrodadium
128
108
51c Conidiophores short, simple or branched, hyaline; larger conidia typically canoe-shaped,
1-celled conidia usually present
Fusarium
130
5 Id Conidiophore tall, slender, simple; conidia with pointed apex
and rounded base
Pyrkularia
128
Steganosporium
194
Epicoccum
150
52a Conidia borne in acervuli in bark
52b Conidia borne typically in small sporodochia
52c Conidia borne on separate conidiophores
53a Conidia attenuate or pointed at apex, often in chains
53b Conidia rounded, borne singly
53
Ahernaria
132
Stemphylium
132
Sclerotium
196
54b No conidiophores, no conidia formed; sclerotia mostly flattened or irregular,
often loose
Rhizoctonia
196
54a No conidiophores, no conidia formed; sclerotia more or less
globose, compact
54c Large conidiophorelike structures present on leaves; many branches
compacted into globose or pointed structures
CristularieUa
74
THE HUGHES-TUBAKI-BARRON SYSTEM OF
CLASSIFICATION
This newer system is based primarily on the development of the conidia and to a lesser extent on the
development of the conidiophores. Shape, pigmentation, and septation of conidia are reduced to
secondary characteristics. Although this classification, followed by Barron (1968), is not complete for all
genera of imperfect fungi, it is well established and accepted by many mycologists and can be applied
accurately to most of the Moniliales. The authors do not dispute the validity of the more recent system of
classification proposed by the Kananaskis Conference (1971) and followed by Ellis (1971), but do not
believe the time has come to shift to that system for the identification of genera by the student.
The following key to series, sections, and genera of the two largest families (Moniliaceae and
Dematiaceae) is included for the convenience of those who can easily recognize and distinguish the types of
conidia. It may not be helpful in identifying those genera in which the mode of conidial formation is
unclear or indefinite. In these cases, use of the key based on the Saccardo System is recommended.
40
ALTERNATE K E Y TO S E R I E S A N D GENERA
(Moniliaceae and Dematiaceae)
Tubercula.riaceae and Stilbaceae, as well as some genera in which there is inadequate knowledge of
conidial formation, are excluded from this key.
Conidia (arthrospores) formed
by segmentation of vegetative hyphae or branches of nonmeristcmatic conidiophores; mature
conidia usually with truncate
ends, ellipsoid or cylindrical . . .
(Examples: Geotrichum, Amblyosporium)... Series ARTHROSPORAE
Arthrosporae,
Geotrichum
lb Conidia (arthrospores) developing in basipetal succession by
meristemic growth of the special
portion of conidiophore, resulting in a gradual change from
conidiophore to conidium; conidia usually, but not necessarily,
hanging together in chains . . .
(Examples: Oidium, Basipetospora) . . . Scries MER1STEM
ARTHROSPORAE
Meristem Arthrosporae, Oidium
41
ALTFRNATF K H Y TO S C R IP S AND GENFRA
Conidia (aleuriospores) usually
single and apical on conidiophore or sporogenous cells,
often thick-walled and pigmented but may be hyaline, often
not easily deciduous or deciduous by means of a special cell
at apex of conidiophore; accessory conidial states often present
. . . (Examples: Humicola, Sepedonium, Microsporum)
Series ALEURIOSPORAE
10
Aleuriosporae, Nigrospora
Conidia (anncllospores) produced
successively on apex of conidiogenous cells or conidiophore
which increases slightly in length
by pereurrent proliferation
through previous conidial scars;
successive scars appear as faint
anncllations at apex of conidiogenous c e l l . . . (Examples; Spilocaea, Scopulariopsis) ... Series
ANNELEOSPORAE
52
Annellosporae, Spilocaea
Conidia (blastospores) developing as buds from simple or
branched conidiophores, or directly from vegetative cells or
previous conidia, often forming
simple or branched acropetalous
chains ... (Examples; Aitreobasidiutn, Montlia, Cladosporium) ...
Series B L A S T O SPORAE
59
Blastosporae, Monilia
AlTERNATE KEY TO SERIES AND GENERA
Conidia (blastospores) produced on well differentiated
swollen cells which bear many
conidia simultaneously, forming
clusters or heads, solitary or in
simple or branched aeropetalous
chains; mature conidia easily
deciduous revealing small denticles on sporogenous cells ...
(Examples: Oecfotvphalum, Boirviis, Gonuiohoirvs)... Series BOf RYOBLASTO'SPORAE
Botryoblastosporae, Batrytis
Conidia (porospores) developing
through pores in outer wall at
apex or side of eonidiophore,
single or in some genera produced
on successive new growing points
formed by sympodial proliferation ... (Examples: Helminthosporium, Bipolarts, Stemphvfium) . . .
Scries P O R O SPORAE
90
Porosporae, Bipo/an's
Conidia (syrnpodulospores) developing at tips of conidiophores
or conidiogenous cells (not from
pores in outer wall) and forming
successively on new growing tips
by sympodial proliferation; increase may be slight but conidia
are of different ages; (this key
includes some genera placed by
some authors in the Porosporae)
.. . (Examples: Fusiclactium,
Tri! irachium,
Ccrcospora)
Series S Y M P O D U L O SPORAE
102
Sympodulosporae, Sporothrix
43
44 ALTERNATE K E Y TO S E R IE S AND GENERA
ti
Conidia (phialospores) formed
successively from open apex of
conidiophore or conidiogenous
cell (phialide), which ordinarily
does not increase in length; conidia often collect in droplet of
mucilage or slime at apex or
remain attached in basipetal
chains; in a few genera the simple conidiophore proliferates
percurrently and forms new
phialides ... (Examples: Chalara, Phialophora, Verticillium,
Aspergillus) .,. Series PHIALOSPORAE.
Phialosporae,
151
Chahra
ARTHROSPORAE
2a Conidiophores poorly developed or none
3
2b Conidiophores distinct and well developed
4
3a Conidia truncate at both ends, formed by segmentation of mycelium
3b Conidia rounded with truncate base, formed by segmentation of
mycelium
Geotrichum
68
Chrysosporium
68
4a Conidiophores simple
5
4b Conidiophores branched
6
5a Conidia globose
5b Comdia cylindrical with truncate ends
6a Conidiophores stout, branched only near apex
6b Conidiophores slender with both apical and lateral branches
Wallemia
92
Ampulliferina
106
Amblyosporium
68
Oidiodendron
68
MERISTEM ARTHROSPORAE
7a Parasitic on plants, powdery mildews
8
7b Saprophytic or weakly parasitic, not powdery mildews
9
8a Conidia in basipetal chains
Oidium
68
Ovulariopsis
70
9a Conidia 1-celled, hyaline
Basipetospora
70
9b Conidia 2-celled, hyaline
Trichothecium
108
9c Conidia dictyosporous, dark
Coniosporium
134
8b Older conidia falling off before new one is formed
ALTERNATE KEY TO SERIES AND GFNERA
45
ALEURIOSPORAE
10a Conidia long, slender (scolecosporous), I- to several-celled
Anguillospora
140
10b Conidia typically 1- to 2-celled, globose to oblong
II
10c Conidia typically 3- to several-celled
24
1 la Conidia hyaline or subhyaline (with slight pigment)
12
lib Conidia with distinct dark pigment
17
12a Pathogenic to man; macroconidia tuberculate
Histoplasma
82
12b Pathogenic to man; macroconidia smooth
Blastomyces
80
12c Saprophytic or parasitic on plants or fungi
13
13a Conidia 1-celled, in small groups at apex of forked conidiophores
Glomerularia
13b Conidia 1- or 2-celled, not in clusters at apex of conidiophores
86
14
14a Conidiogenous cells slender, radiating from swollen cell
14b Conidiogenous cells short, stout; conidia smooth
Umbelopsis
86
Botryoderma
86
I4c Conidiogenous cells slender; conidia rough-walled or with attached smooth cells
15
15a Conidia with attached small smooth cells
Stephanoma
82
15b Conidia 1-celled, without attached smooth cells
Sepedonium
82
15c Conidia with large apical rough-walled cell and smaller smooth basal cell
16a Basal cell of conidia rounded
16b Basal cell wedge-shaped
16
Mycogone
82
Chlamydomyces
82
17a Conidiophores short, poorly developed, or missing
18
17b Conidiophores usually well developed
22
18a Conidia with broad truncate base and pointed apex
18b Conidia ovoid to obclavate with rounded apex
Echinobotryum
84
Asteromyces
84
18c Conidia globose to broadly ellipsoid
19
19a Conidia 1-celled, subglobose, shiny black, situated on a flat hyaline vesicle .. Nigrospora
82
19b Conidia 2- or more-celled
20
19c Conidia I-celled, light to dark, not on vesicle
21
20a Conidiophores tall, slender, simple, dark
Endophragmia
118
20b Conidiophores mostly short, simple hyaline
Trichocladium
118
Balanium
106
21a Setae present
Botryotrichum
84
21b Setae absent
Humkola
84
Stephanoma
82
20c Conidiophores well developed, branched
22a Conidia with small hyaline cells attached
46
ALTERNATE KEY TO SERIES A N D GENERA
22b Conidia without attached hyaline cells
23
23a Conidiophores short, thick, branched
23b Conidiophores tall, slender, repeatedly branched
23c Conidiophores tall, simple
Wardomyces
84
Staphylotrichum
80
Microclavia
80
24a Conidia typically 3- to several-celled (phragmosporous)
25
24b Conidia with cross and oblique septa (dictyosporous
34
24c Conidia (or propagules) branched (staurosporous)
38
24d Conidia curved or coiled (helicosporous)
Xenosporium
136
25a Conidia hyaline or subhyaline
26
25b Conidia with distinct dark pigment
29
26a Parasitic on plants
26b Causing
dermato
Fusoma
mycoses
of
man
or
animals
26c Saprophytic or trapping nematodes
28a Conidia ellipsoid, with broad enlarged middle cell
Microsporum
116
Monacrosporium
118
28b Conidia cylindrical to long and sometimes tapering, with distinctly enlarged middle
cell
Daciylella
29a Conidia ovoid to ellipsoid to oblong
128
30
29b Conidia much longer than wide
,
32
Endophragmia, Phragmocephala
118
Bactrodesmium
150
30b Conidiophores short, poorly developed, clustered
30c Conidiophores usually short, single
31
31a Conidia mostly 2- to 3-celled; ovoid to clavate
31 b Conidia 3- to several-celled; broadly ellipsoid wall not unusually thick
31c Conidia several-celled, ellipsoid, wall very thick
32a Conidia cylindrical
32b Conidia narrower at ends, especially at apex
27
28
27a Macroconidia spindle-shaped or ellipsoid
30a Conidiophores tall, simple, single or clustered
116
Trichocladium
118
Pithomyces
132
Murogeneila
114
Camposporium
116
33
,
33a Apical cell of conidia attenuated, hooked or pointed
33b Apical cell of conidia rounded, not attenuated
Ceratophorum
118
Clasterosporium
118
34a Conidiophores clustered, sometimes in loose sporodochia
35
34b Conidiophores single, not clustered
36
•
AlTFRNAi'E K F Y TO S F R IE S AND GENFRA
47
Epicoccum
Berkleasmium
150
134
Apical cell of conidia darker, much enlarged
Apical cell of conidia not enlarged, equally pigmented
Acrospeira
132
37
37a
37b
Conidia broadly ellipsoid, most septa transverse
Conidia globose to ovoid, most septa oblique
Pithomyces
Stigmella
132
134
38a
38b
Conidia hyaline or subhyaline
Conidia with distinct dark pigment
39a
39b
39c
Propagule with many branches compacted into a large globoid or
conical structure; no true conidia produced
Conidia with few branches, symmetrical or nearly so
Conidia with few branches distinctly asymmetrical
40a
40b
Main axis of conidia distinctly swollen, with large cell
Main axis of conidia slender or short, without swollen cell
35a
35b
Conidia globose or subglobose
Conidia large, elongate to obovoid
36a
36b
39
49
Cristulariella
74
40
43
41
42
Actinospora
Clavariopsis
140
140
Tetrachaetum
Triscelophorus
Tridentaria
140
138
140
Thaltospora
142
44
41a Central cell of conidia globose, with 4 slender radiating arms
41 b Main axis of conidia 2-celled, with 3 slender radiating arms
42a
Alb
42c
Main axis of conidia long, slender
Main axis of conidia short; arms widely divergent
Main axis of conidia short; arms not widely divergent
43a
43b
Not aquatic, parasitic on higher plants
Aquatic, in fresh water on decaying leaves
44a
44b
Branches of conidia developed one at a time
Branches of conidia developed simultaneously
45a
45b
Conidia with 3 slender branches on slender main axis
Conidia with 3 slender branches on thick main axis
46a
46b
Conidia with 2 branches arising from primary axis
Conidia with 3 or more branches arising from primary axis
47a
Alb
48a
48b
Branches
of
conidia
long,
tapering
to
Branches of conidia slender but not tapering to fine point
Branches of conidia more or less upright
Branches of conidia widely divergent, irregular
49a
49b
Conidiophores distinct; conidia triangular or with several upright branches
Conidiophores reduced to a short peg; conidia with 2 to 3 upright or spreading "horns"
50a
Conidia triangular, with 3 short, radiating arms
45
46
Articulospora
Culicidospora
142
140
47
48
fine
point
fngoldia
Tricladium
Tetracladium
Dendrospora
Triposporium
138
138
140
140
50
51
144
48
ALTERNATE K E Y TO S E R I E S A N D GFNLRA
50b Conidia with several close upright branches
51a Mostly parasitic on leaves
51b Mostly saprophytic on wood
Dictyosporium
144
Hirudinaria
144
Ceratosporium
144
ANNELLOSPORAE
52a Conidia typically 1- to 2-celled
53
52b Conidia mostly 3- to several-celled
55
53a Conidiophores hyaline
Scopulariopsis
53b Conidiophores dark
54a Conidiophores tall, branched; conidia in moist heads
54b Conidiophores short, simple, not in heads
55a Conidia with 2 or more upright branches
98
54
Leptographiwn
98
Spihcaea
106
Ceratosporella
144
55b Conidia unbranched
56
56a Mostly parasitic; mycelium within leaves; conidiophores short
57
56b Saprophytic or with external mycelium; conidiophores short
58
57a Conidiophores single, arising from epidermal cells
Deightonielh
118
57b Conidiophores clustered, arising through stomata
Stigmina
120
Endophragmia
118
Annellophora
118
58a Conidiophore apex with distinct cuplike structures
58b Conidiophore apex with conidial scars or rings, not cuplike
BLASTOSPORAE
59a Conidiophores arising from basal globose mother cells, with thick dark septa, increasing
in length only in basal region
60
59b Conidiophores, if present, not as above
61
60a Conidia 1-celled
60b Conidia 4-celled, cross-shaped
Arthrinium
74
Dictyoarthrinium
134
61a Conidia more or less coiled (helicosporous)
62
61 b Conidia branched (staurosporous)
63
61c Conidia neither coiled nor branched
66
62a Small conidia produced by budding of large conidia
62b Conidia not budding
Helkodendron
136
Helkoon
136
63a Conidiophores present, distinct
64
63b Conidiophores absent
65
ALTERNATE KEY TO SERIES AND GENERA
49
64a Conidia hyaline, with slender divergent arms
Varicosporium
138
64b Conidia dark, branches more or less upright
Speiropsis
142
Tetraploa
142
TYipospermum
142
66a "Conidiophores" (propagules) compactly branched, globose to conical, ultimate cells
globose, conidialike; no true conidia produced
Cristulariella
74
66b Conidiophores poorly formed or reduced to pegs or short conidiogenous cells
67
66c Conidiophores distinct, simple or loosely branched
70
65a Conidia with 3 to 4 upright to spreading branches
65b Conidia with 4 to 5 widely divergent branches
67a Mycelium with clamp connections; conidia forcibly discharged
Itersonilia
67b With neither clamp connections nor forcibly discharged conidia
68a Parasitic on grasses; conidia 2-celled, not budding
70
68
Rhynchosporium
68b Usually saprophytic; conidia !-celled, budding
108
69
69a Mycelium and conidia hyaline
Candida
69b Mycelium and conidia with dark pigment
70a Conidia hyaline, 2-celled
70
Aureobasidium
70
Trichothecium
108
70b Conidia hyaline or subhyaline, 1-ceIIed
71
70c Conidia with distinct dark pigment
74
71a Conidia borne in acropetalous chains
72
71 b Conidia not in chains
73
!
72a Conidiophores dark; conidia in moist heads
Haplographium
80
72b Conidiophores hyaline; conidia uniform globose to short ellipsoid, in long branched
chains
Manilla
72
72c Conidiophores hyaline branched; conidia variable, in short chains
72
72d Conidiophores subhyaline, conidia elongate, slender
Hyaiodendron
Tilletiopsis
72
73a Conidiophores dark; conidia ovoid, 2 to 3 on each swollen dark cell
Zygosporium
72
73b Conidiophores hyaline; conidia lunulate, not clustered
Lunulospora
138
73c Conidiophores hyaline; conidia globose to broad ellipsoid, single, apical on long
denticles
Olpitrichum
74
74a Conidia all or mostly 1-celled
75
74b Conidia mostly 2-celled
77
74c Conidia 3- to several-celled (phragmosporous)
75a Conidia variable, some typically lemon-shaped
75b Conidia uniform, mostly ovoid to ellipsoid
75c Conidia uniformly globose
,
78
Cladosporium
106
Papularia
82
76
50 ALTERNATE K F Y TO S E R IE S A N D GFNERA
76a Setae present; apex of conidiophore globose
LaceHinopsis
78
76b Setae present; apex of conidiophore not enlarged
Lacellina
78
76c Setae absent
Periconia
74
Cladosporium
106
Bispora
106
11a. Conidiophores branched; conidia variable
lib
Conidiophores mostly simple; conidia uniformly ellipsoid
78a Conidia borne on special globose cells
79
78b Conidia not borne on special globose cells
80
79a Conidia catenulate
Pseudotorula
116
Dwayabeeja
116
Septonema
116
79b Conidia not catenulate
80a Conidia catenulate, cylindrical
80b Conidia catenulate, cells strongly rounded
80c Conidia not catenulate
Torula
Gonatophragmium
74
122
BOTRYOBLASTOSPORAE
81 a Conidia in simple or branched chains of 2 or more
82
81b Conidia not catenulate
83
82a Conidiophores tall, dark; conidia dark
82b Conidiophores variable, hyaline; conidia hyaline
83a Conidia dark, phragmosporous
Gonatobotryum
Gonatorrhodiella
78
78
Cephaliophora
116
83b Conidia hyaline, 1-celled
84a Conidiophores short, reduced to 1 or few cells
84
Phymotolrichum
78
84b Conidiophores tall, well developed
85
85a Conidiogenous cells globose or with globose lobes
86
85b Conidiogenous cells or fertile portion of conidiophore elongated to irregular
89
86a Conidiophores simple or with few branches
87
86b Conidiophores with several branches, at least near apex
88
87a Conidiophores determinate, with a single head of conidia
87b Conidiophores proliferating percurrently, with several clusters of
conidia
88a Conidiophore branches many, lateral on main axis
88b Conidiophore branches regularly dichotomous
88c Conidiophore branches irregular
89a Conidiophore branches dichotomous near apex
89b Conidiophore branches irregular
Oedocephalum
76
Gonatobotrys
76
Botryosporium
76
Dichobotrys
Botrytis
78
76
Chromelosporium
Aciadium
80
76
AUERNATL K E Y TO S F R Ifc S A N D GENERA 51
POROSPORAE
90a Conidia with transverse and oblique septa (dictyosporous)
91
90b Conidia with transverse septa only (phragmosporous)
93
90c Conidia 2-celled, catenulate
91a Conidia long-beaked, obclavate, or ovoid
Diplococcium
114
Allernaria
132
91 b Conidia not beaked, globose to broadly ellipsoid
92
92a Conidiophores elongating sympodially
Ulocladium
132
92b Conidiophores elongating percurrently
Stemphylium
132
93a Conidiophores tall, branched; conidia catenulate
Dendryphion
124
93b Conidiophores tall, branched; conidia not catenulate
94
93c Conidiophores mostly simple
96
94a Conidiophores dichotomous near apex; conidia mostly severalcelled
Dichotomophthora
120
94b Conidiophores not dichotomous near apex
95a Conidia mostly 3-celled
95
Spondylocladiella
120
Dendryphiopsis
120
95b Conidia 4- to several-celled
96a Conidia in acropetalous chains, often breaking up into 1- to several-celled
fragments
Torula
74
96b Conidia not catenulate
97
97a Conidiophores indeterminate, extending sympodially
98
100
97b Conidiophores determinate
98a Conidia bent by enlargement of one cell
Curvularia
98b Conidia not bent by enlarged cell, straight or slightly curved
99a
99b
99
Mid-cells of conidia larger than end cells; germ tubes originate from any
cell
Drechslera
122
Mid-cells of conidia not distinctly larger than others; germ tubes only from end
cells
Bipolaris
126
100a Conidiophores clustered; conidia apical
Exosporium
100b Conidiophores single; conidia apical and lateral
100c
122
Conidiophores single; conidia single, apical
101a Conidia several-celled, cylindrical to obclavate
101b Conidia often less than 4-celIed, ellipsoid to obovoid
148
101
Corynespora, Sporidesmium
120
Helminthosporium
124
Spadicoides
114
52 ALTERNATE K E Y TO S E R I F S AND GENERA
SYMPODULOSPORAE
Note: The key to this section includes some genera described as producing porospores and in which
the conidiophores commonly extend by sympodial growth.
102a Conidia coiled, helicosporous
103 -
I02b Conidia not coiled
106
103a Conidia thick in proportion to length, not hygroscopic
105
103b Conidia thin in proportion to length, hygroscopic
104
104a Parasitic on higher plants; some conidia nearly straight
Helicomina
136
104b Saprophytic on wood or bark; conidia uniformly coiled
Heiicoma
136
Helicomyces
136
Helicosporium
136
105a Conidiophores and conidia hyaline
I05b Conidiophores dark; conidia pale to dark
106a On living plants in nature, principally on leaves, mostly parasitic
107
106b Closely associated with other fungi, often parasitic on them
122
106c Saprophytic on various substrata
123
107a Conidia hyaline or subhyaline
108
107b Conidia distinctly pigmented, pale brown to dark
116
108a Conidia predominantly 1-celled
109
108b Conidia typically 2- to several-celled
Ill
109a Conidiophores relatively short, simple
Idriella
I09b Conidiophores tall, repeatedly branched near apex
102
110
110a Conidia collecting in moist slimy heads
Verticicladiella
104
110b Conidia dry, not in moist heads
Verticicladium
104
11 la Conidia catenulate in acropetalous chains
112
111b Conidia not catenulate
113
112a Conidia mostly 2-celled, with some 1-celled
Ramularia
112b Conidia mostly with 3 or more cells
Septocylindrium
110
128
113a Conidia filiform to cylindrical or long ellipsoid
114
113b Conidia shorter, ovoid to pyriform or short ellipsoid
115
114a Conidiophores hyaline; conidia with attenuated apical cell
Spermospora
128
114b Conidiophores hyaline; conidia! cell not attenuated
Cercosporetta
128
114c Conidiophores dark; conidial cell not distinctly
attenuated
115a Conidia broader near base; cells unequal
Cercospora, Cercosporidium
Pyricularia
128,122
128
ALTERNATE K E Y TO S E R I F S A N D GENERA 53
115b Conidia oblong; cells nearly equal
Didymaria
110
116a Conidiophores tall, dark, simple below, branched near apex and bearing a number of
conidiogenous cells
Periconiella
104
116b Conidiophores and conidiogenous cells not as above
117
! 17a Conidia mostly 1- to 2-celIed
118
117b Conidia 3- to several-celled (phragmosporous)
121
118a Conidia rough-walled, cells equal
Asperisporium
118b Conidia smooth, cells unequal
I I9a Conidiophores distinctly wavy in appearance
119
Polythrincium
\ 19b Conidiophores often irregular but not distinctly wavy
120a Conidiophores usually arise from beneath cutical layer
112
112
120
Fusicladiwn
112
120b Conidiophores emerging through stomata or from surface of
leaves
Scolecotrichum, Passalora
112
121a Conidia with 1 to 4 hyaline appendages on apical cells
Pleiochaeta
128
Nakataea
128
Calcarisporium
102
Dactylium
130
Cladosporietta
92
121b Conidia without appendages
122a Conidiophores and conidia hyaline; conidia 1-celled
122b Conidiophores and conidia hyaline; conidia 3- to 4-celled, mostly ovoid
122c Conidiophores and conidia dark; conidia long, slender
123a Conidia hyaline to subhyaline (slightly pigmented)
124
J23b Conidia with distinct dark pigment
139
124a Conidia typically 1-celled
125
124b Conidia typically 2-celled
135
124c Conidia 3- to several-celled
137
125a Conidiophores variously branched, rarely simple
126
125b Conidiophores typically simple, rarely branched
131
126a Conidiophores branched only near apex
127
126b Conidiophore branches lower or lateral on main axis
128
127a Conidia in moist heads of slime
Verticicladiella
104
I27b Conidia dry, not in moist heads
Verlicicladium
104
128a Conidiophore branches verticillate on main axis
129
128b Conidiophore branches irregular; conidiogenous cells may be verticillate
130
129a Conidiophores hyaline; conidia ovoid
I29b Conidiophores pigmented; conidia long, slender
Tritirachium
100
Selenosporella
102
54 ALTFRNATE K E Y 10 SERIfS AND GFNERA
130a Fertile area of conidiogenous cell slender, not enlarged
Hamfordia
98
130b Fertile area of conidiogenous cell somewhat enlarged, at least at apex .. Nodulosporium
100
130c Fertile area of conidiogenous cell much elongated; not enlarged
Geniculosporium
100
Sympodiella
104
13la Conidia catenulate
131b Conidia not catenulate
-132
132a Fertile area of conidiogenous cell slender, rachislike
133
132b Fertile area of conidiogenous cell not slender or rachislike
134
133a Base of conidiophore enlarged; mostly on insects
133b Base of conidiophore not enlarged; saprophytic
134a Conidiophores slender, hyaline, single, only slightly enlarged at apex
134b Conidiophores pigmented, single, greatly enlarged at apex
134c Conidiophores hyaline, in clusters
135a Apical cell of conidium equal to or smaller than basal cell, sometimes
elongated
Beauveria
100
Tritirachium
100
Sporothrix
98
Basidiobotrys
100
Ovularia
104
Dactylaria
110
135b Apical cell of conidium larger or wider than basal cell, rounded
136
136a Conidia in loose clusters, on short denticles
Arihrobotrys
110
136b Conidia in loose clusters, on long pegs
Candelabrelta
110
136c Conidia single on sympodial branches of conidiophore
Genicularia
110
137a Conidia forked, with 2 parallel prongs
Dkranidion
138
I37b Conidia not forked
138
138a Conidiophores short, hyaline; conidia cylindric to clavate
Dactylaria
110
138b Conidiophores tall, hyaline; conidia cylindric to fusoid
Dactylella
128
Pleurothecium
126
139a Conidiophores tall, dark, slender, bearing at apex several divergent conidiogenous
cells
Pseudobotrylis
106
139b Conidiophores and conidiogenous cells not as above
140
140a Conidia 1-celled
141
I4()b At least some conidia 2- or more-celled
147
138c Conidiophores tall, dark; conidia fusoid
141a Conidia biconie, tapering toward both ends
Beltrania
141b Conidia otherwise
142a Conidia oblong-elongate
104
142
Selenosporella
102
I42b Conidia mostly globose or ovoid
143
143a Conidia symmetric, both sides rounded
144
143b Conidia asymmetric, one side flat or concave
Virgaria
100
ALTERNATE KEY TO SERIES AND GENERA
144a
55
Conidiophores branched irregularly; conidiogenous cells somewhat enlarged, at least at
apex
Noduhsporium
100
144b
Conidiophores simple or branched; conidiogenous cells not enlarged at apex
145
145a
Conidiophore branches somewhat spiral, appearing wavy
145b
Conidiophores or branches more or less straight, not wavy
146a
Conidiophores or conidiogenous cells, short, mostly ] - to 3-celled
Conoplea
102
Rhinocladiella
104
147
146b Conidiophores tall, well developed
148
147a
Conidia 1- to 2-celled, ovate, oblong or T-shaped
Scolecobasidium
147b
Conidia staurosporous, several-celled, Y-shaped, with 2 pointed arms
147c
Conidia staurosporous, with 3 or more branches
148a
Conidia dictyosporous, some phragmospores present
Diplocladiella
142
Speiropsis
142
Dactylosporium, Sirosporium
148b Conidia typically phragmosphorous
149a
Conidia often catenulate
114
134
149
Heterosporium
149b Conidia not catenulate
122
150
150a
Conidia attached by slender pedicels to apex of conidiophores
Brachysporium
126
150b
Conidia attached directly to hyaline apex of conidiophores
Cacumisporium
124
PHIALOSPORAE
151a Normally aquatic, growing on decaying vegetation
152
151b Not normally aquatic
154
152a
153
Conidia or branches long, slender
152b Conidia unbranched
153a
Conidia long, slender, unbranched
153b Conidia each with 4 slender arms
154a
Heliscus
108
Flagellospora
138
Lemonniera
138
Conidia typically 2- to several-celled
155
154b Conidia typically I-celled
159
155a
156
Conidiophores with dark pigment
155b Conidiophores (or conidiogenous cells) hyaline
156a
Conidiophores tall with lateral branches and sterile apex; conidia not
catenulate
157
Chaetopsis
96
Conidiophores with few branches near apex; conidia catenulate but not end to
end
Fusariella
130
156c
Conidiophores simple; conidia endogenous in end-to-end chains
130
157a
Conidiophores repeatedly branched; one sterile branch typically with swollen
apex
Cylindrodadium
156b
Sporochisma
108
56
ALTERNATF KEY TO SCRIES AND GENERA
157b Conidiophores simple or irregularly branched; without sterile branches
158a Conidia mostly cylindrical, straight, 2- to several-celled
158
Cylindrocarpon
130
158b Conidia ovoid, 2-celled, not in slime heads
Cladobotryum
108
158c Conidia ovoid, 2-celled, in small slime heads
Diplosporium
108
Fusarium
130
159a Apex of conidiophore much enlarged, covered with flask-shaped phialides; conidia in
dry chains
Aspergillus
94
158d Macroconidia typically canoe-shaped, several-celled; microconidia 1-celled
159b Conidiophores, phialides or conidia otherwise
160
160a Conidia hyaline or subhyaline
161
160b Conidia distinctly pigmented, at least in mass
178
161a Conidia crescent-shaped, typically with hyaline apical appendages
162
161b Conidia globose, ovoid, oblong, or hooked, without appendages
163
162a Apical collarette of phialide small, inconspicuous
162b Apical collarette of phialide large, flaring
Menispora
88
Codinaea
88
163a Conidia produced well within phialide (endogenous), mostly rod-shaped
164
163b Conidia produced at apex of phialide, not rod-shaped
167
164a Dark aleuriospores (chlamydospores) also present
165
164b Dark aleuriospores absent
166
165a Aleuriospores rounded, 1-celled, single or in short chains
165b Aleuriospores cylindrical, breaking up into 1-celled fragments
166a Tall dark setae present
166b Dark setae absent
Chalaropsis
90
Thielaviopsis
92
Chaetochalara
90
Chalara
90
167a Conidiophores short or mostly reduced to a single phialide
168
167b Conidiophores well developed, simple or branched
169
168a Conidia in dry chains, no slime present
168b Conidia in small, moist, slimy heads
Monocilliwn
86
Cephalosporium
94
169a Conidia dry, not in moist heads
170
169b Conidia held together in moist slimy heads
172
170a Conidiophores mostly simple, dark; conidia single or catenulate
Monihchaetes
86
170b Conidiophores branched, dark; conidia catenulate
Thysanophora
96
170c Conidiophores branched, hyaline; conidia catenulate
171a Conidia cylindrical, aggregated into dry columns
171
Metarrhizium
94
ALTERNATE K E Y TO SERIFS AND GENERA 57
171b Conidia globose, ovoid or rod-shaped; conidiophore "brush" compact
1 7 lc Conidia fusiform to lemon-shaped; conidiophore "brush" loose
Penkillium
94
Paecilomyces
94
172a Conidiophores simple or reduced to short, 1-celled phialides
173
172b Conidiophores variously branched, at least at apex
174
173a Conidiophores dark; coiled setae absent
173b Conidiophores (phialides) hyaline; coiled setae present, unbranched
173c Conidiophores (phialides) hyaline, with coiled branched setae
Chloridium
88
Circinotrichum
90
Gyroihrix
90
174a Conidial masses large, only at apex of conidiophore
175
174b Conidial masses small, at apex of conidiophore
177
175a Conidiophores hyaline, apex often enlarged, branches Aspergillus-Iike
176
175b Conidiophores hyaline, branches Penicillium-like
Gliocladium
92
Phiahcephala
96
Gliocephalotrichum
94
Gliocephahs
94
Verticillium
92
177b Conidiophores hyaline, branches irregular
Trichoderma
92
177c Conidiophores dark, branches arising at points on main axis
Gonylrichum
98
175c Conidiophores dark, branches Penicillium-like
176a Conidial mass subtended by sterile arms
176b Conidial mass not subtended by sterile arms
177a Conidiophores hyaline, branches (or phialides) verticillate
178a Conidiophores mostly reduced to phialides
179
178b Conidiophores well developed
180
179a Phialides slender, tapering upward; collarette not evident
Gliomastix
86
Phiahphora
88
180a Upper portion of conidiophores branched; phialides long, slender; conidia dark, in
small, moist heads
Stachylidium
92
180b Upper portion of conidiophores branched; conidia dry, dark, lemon-shaped,
catenulate
Phialomyces
94
179b Phialides cylindrical to inflated; collarette often flaring
180c Conidiophores unbranched; short thick phialides at base of simple conidiophores
181
181a Conidia in moist slimy heads, not catenulate
Stachybotrys
88
18lb Conidia not in slimy heads, catenulate
Memnoniella
88
ALTERNATE K E Y TO SERIFS AND GENERA 57
171b Conidia globose, ovoid or rod-shaped; conidiophore "brush" compact
1 7 lc Conidia fusiform to lemon-shaped; conidiophore "brush" loose
Penkillium
94
Paecilomyces
94
172a Conidiophores simple or reduced to short, 1-celled phialides
173
172b Conidiophores variously branched, at least at apex
174
173a Conidiophores dark; coiled setae absent
173b Conidiophores (phialides) hyaline; coiled setae present, unbranched
173c Conidiophores (phialides) hyaline, with coiled branched setae
Chloridium
88
Circinotrichum
90
Gyroihrix
90
174a Conidial masses large, only at apex of conidiophore
175
174b Conidial masses small, at apex of conidiophore
177
175a Conidiophores hyaline, apex often enlarged, branches Aspergillus-Iike
176
175b Conidiophores hyaline, branches Penicillium-like
Gliocladium
92
Phiahcephala
96
Gliocephalotrichum
94
Gliocephahs
94
Verticillium
92
177b Conidiophores hyaline, branches irregular
Trichoderma
92
177c Conidiophores dark, branches arising at points on main axis
Gonylrichum
98
175c Conidiophores dark, branches Penicillium-like
176a Conidial mass subtended by sterile arms
176b Conidial mass not subtended by sterile arms
177a Conidiophores hyaline, branches (or phialides) verticillate
178a Conidiophores mostly reduced to phialides
179
178b Conidiophores well developed
180
179a Phialides slender, tapering upward; collarette not evident
Gliomastix
86
Phiahphora
88
180a Upper portion of conidiophores branched; phialides long, slender; conidia dark, in
small, moist heads
Stachylidium
92
180b Upper portion of conidiophores branched; conidia dry, dark, lemon-shaped,
catenulate
Phialomyces
94
179b Phialides cylindrical to inflated; collarette often flaring
180c Conidiophores unbranched; short thick phialides at base of simple conidiophores
181
181a Conidia in moist slimy heads, not catenulate
Stachybotrys
88
18lb Conidia not in slimy heads, catenulate
Memnoniella
88
DESCRIPTIONS AND ILLUSTRATIONS
OF GENERA
60
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
HELICOCEPHALUM Thaxt. Conidiophores upright, long, slender, simple, nonseptate; conidia produced in a spiral, forming a head held in a slime drop, 1-celled, ellipsoid, hyaline or slightly pigmented;
saprophytic on dung or decaying wood.
Illustration: (A) H. sarcophilum; redrawn from Thaxter (438); (B) H. oiigosporum; original, from
material on decayed wood. Other reference (98).
RHOPALOMYCES Corda. Mycelium sparse; conidiophores upright, slender, simple; conidia borne on
enlarged tip of conidiophore, which is hexagonally aerolate, 1-celled, hyaline, ellipsoid; saprophytic on
plant material, or destroying nematode eggs.
Illustration: R. strangulatus; redrawn from Thaxter (436). (A) conidiophore and head of conidia;
(B) head of conidia enlarged; (C) conidia. References (36).
CUNNINGHAMELLA Matr. Mycelium white, extensive in culture, nonseptate; conidiophores
(sporangiophores) simple or branched, with enlarged tips bearing heads of conidia (sporangioles); conidia
hyaline, 1-celled, globose; common saprophytes in soil.
Illustration: C. elegans; original, from pure culture. (A) simple conidiophore and head of conidia;
(B) branched conidiophore; (C) detail of tip of conidiophore showing denticles; (D) conidia. References
(70, 171).
MYCOTVPHA Fenncr. Mycelium at first nonseptate, later becoming septate, hyaline; conidiophores
(sporangiophores) erect, tall, simple, septate; head of spores cylindrical; conidia (sporangioles) i-celled,
borne singly on short denticles; saprophytic.
Illustration: M. microspora; original, from culture. (A) group of conidiophores; (B) head of conidia
enlarged; (C) conidia. Reference (132).
MORTIERELLA Coemans. Mycelium typically appressed to substrate, fine; conidiophores (sporangiophores) hyaline, simple or branched, typically tapering upward; conidia (sporangioles) globose, hyaline,
single, apical; typical multispored sporangia present in some species, absent in others; common in
soil, saprophytic.
Illustration: Mortierella sp; original from culture. Reference (136).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
RHOPALOMYCES
MORTIERELLA
CUNNINGHAMELLA
61
62
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
SYNCEPHALIS Van Teigh. and Le Monn. Conidiophores (sporangiophores) upright, straight or bent
near the apex, with prominent rhizoids at the base; apex enlarged, producing branches, bearing rodlike
sporangioles which break up to form short conidia; parasitic on other Mucorales.
Illustration: S. pycnosperma. (A) general habit of nearly mature fertile hypha; (B) formation of separate
spores; redrawn from Thaxter (440). Other reference (17).
PIPTOCEPHAL1S de Bary. Conidiophores (sporangiophores) erect, septate, repeatedly dichotomously
branched, tips more or less swollen, deciduous, bearing cylindrical, rodlike sporangioles; sporangioles
break up into short conidia at maturity; haustorial parasites on other fungi, principally Mucorales.
Illustration: P. virginiana; original, from a culture on Mucor. (A) conidiophore and sporangioles; (B)
heads of spores; (C) chains of spores breaking apart; (D) haustorium of parasite in host mycelium.
References (22, 256).
COEMANSIA Van Tiegh and Le Monn. Mycelium sparse, nonseptate; conidiophores upright, slender,
septate, sparingly branched, at intervals bearing sporocladia that produce conidia only on the lower
(outer) surface; conidia hyaline, 1-ceIIed, ovoid to fusoid; saprophytic on dung.
Illustration: C. erecta; (A) conidiophores; (B) sporocladia and conidia; redrawn from Linder (268). Other
reference (22).
DIMARGARIS Van Tieghem. Conidiophores (sporangiophores) erect, septate, at first simple, becoming
irregularly cymosely or verticillately branched and producing fertile terminal heads; sterile branches
absent; conidial heads composed of many sporogenous branchlets, consisting of short chains of cells
formed by budding, each cell giving rise to a whorl of 2-spored sporangioles; conidia finally separating,
immersed in liquid at maturity, ellipsoid or rod-shaped; parasitic on other Mucorales, producing branched
haustoria.
Illustration: D. vertkillata; redrawn from Benjamin (23). (A) upper portion of sporangiophore;
(B) enlarged branch apex; (C) branchlet with several 2-spored sporangioles; (D) conidia.
TIEGHEMIOMYCES Benjamin. Conidiophores (sporangiophores) erect, septate, simple below, giving
rise above to fertile branch systems; branches septate, several repeatedly, irregularly branched, the ends
consisting of fertile cells bearing whorls of 2-spored sporangioles; conidia finally separating, smooth
subglobose to ovoid, dry at maturity; parasitic on other Mucorales, producing branched haustoria.
Illustration: 7 ." caHfornicus; redrawn from Benjamin (23). (A) habit of sporangiophores; (B) branch of
sporangiophore; (C) branchlets with 2-spored sporangioles; (D) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
SYNCEPHAUS
COEMANSIA
PIPTOCEPHALIS
TIEGHEMIOMYCES
63
64
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
RADIOMYOES Embree. Conidiophores (sporangiophores) borne singly or sometimes in pairs near the
ends of stolons that terminate in rhizoid systems; conidiophores dark brown, terminating tn primary
vesicles bearing radiate stalks and secondary vesicles; conidia borne on tertiary stalks, subglobose to
ellipsoid, conidia hyaline, reniform to oblong-ellipsoid; saprophytic.
Illustration: R. embreei; (A) apex of conidiophore with conidia! head; (B) single branch of conidial head;
(C) single branch void of conidia; (D) conidia; redrawn from Benjamin (24). Other reference (127).
MARTENSELLA Cocmans. Mycelium sparse; conidiophores upright, simple, bearing lateral or apical
sporocladia; conidia borne on upper surface of sporocladia, hyaline, l-celled; saprophytic.
Illustration: M. corticii; (A) conidiophores; (B) sporocladia and conidia; redrawn from Jackson and
Dearden (240). Other references (22, 268).
KICKXEELA Coemans. Mycelium sparse; conidiophores simple with an apical disk bearing sporocladia;
conidia produced on the upper surface of sporocladia, hyaline, I-celled; saprophytic on horse dung.
Illustration: K. alahastrina; (A) conidiophore; (B) sporocladium and ctfnidia redrawn from Benjamin
(22). Other reference (268).
L1NDERINA Rapcr and Fennell. Conidiophores long, septate, branched, bearing several domelike
sporocladia with pseudophialides and conidia on the upper surface; conidia hyaline, l-celled, elongated;
saprophytic in soil.
Illustration: L. pennispora; (A) diagram showing habit of growth; (B) a single sporocladium; redrawn
from Raperand Fennell (348).
MARTENSIOMYCES Meyer. Conidiophores (sporangiophores) erect or ascending, becoming irregularly cymosely branched; sporocladia stalked, borne in umbels on recurved branchlets, producing pseudophialides on one side (resembling Coemansid)\ pseud ophialides ellipsoid, each bearing a single conidium
(sporangiole); conidia obclavate, hyaline, enveloped in liquid at maturity; saprophytic, from soil.
Illustration: M. pterosporus; redrawn from Benjamin (23). (A) conidiophore; (B) group of sporocladia;
(C) sporocladium; (D) conidium.
SPIRODACTYEON Benjamin. Conidiophores (sporangiophores) erect or ascending, septate, giving rise
above to coiled, fertile branches; sporocladia borne successively on the lower surface of the coils, septate,
with narrowed apices, producing laterally pseudophialides that bear single sporangioles (conidia); conidia
short-ellipsoid, not enveloped in liquid at maturity; saprophytic on dung.
Illustration: S. aureum; redrawn from Benjamin (22). (A) conidiophore; (B) group of sporocladia;
(C) sporocladium bearing conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
RADIOMYCES
MARTENSELLA
*
MARTENSIOMYCES
SPIRODACTYLON
65
66
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
SYNCEPHALASTRUM Schroet. Mycelium growing rapidly, abundantly branched; conidiophores
(sporangjophores) erect, branched, tips enlarged, bearing a head of rod-shaped sporangioles, each
producing a row of nearly spherical conidia; wall of sporangiole dissolving to release conidia; saprophytic.
Illustration: S. racemosum; original, from pure culture. (A) conidiophore and head of spores;
(B, C) heads of sporangioles and developing conidia, (D-G) stages in formation and release of conidia.
References (23, 439).
DISPIRA Van Tiegh. Conidiophores (sporangiophores) erect, branched, the sterile branches slender and
spiral, fertile branches enlarged, bearing a head of cylindrical sporangioles that produce rows of short
conidia, parasitic on other Mucorales and one species on Chaetomium.
Illustration: D. cornuta. (A) terminal portion of fertile hypha; (B) portion of fertile head showing
conidia; redrawn from Thaxter (438). Other references (26).
CHOANEPHORA Currey. Mycelium white, extensive and growing rapidly in culture; conidiophores
(sporangiophores) long, enlarged, and branched at the apex, each branch bearing a head of conidia
(sporangioles); conidia 1-celled, brown or purplish, ellipsoid; sporangia typical of the Mucorales also
formed in culture; parasitic on flowers and fruits, or saprophytic, principally curcurbits.
Illustration: C. curcurbitarum; original, from culture. (A) conidiophores; (B, D) portion of head of
conidia; (D) conidia. References (136, 172, 335, 474, 475).
SPIROMYCES Benjamin. Conidiophores arising from substrate hyphae, forming a loose spiral as they
develop upward, septate, each segment giving rise to 2 to 3 short, stout sporocladia, each of which forms a
loose cluster of conidia (sporangioles) on terminal globose enlargements on denticles; conidia subglobose
to globose; saprophytic.
Illustration: S. minuius; redrawn from Benjamin (23). (A) portion of conidiophore; (B) enlarged fertile
branches.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
I
D
,
E
F
D
oo
o o
SYNCEPHALASTRUM
CHOANEPHORA
SPIROMYCES
tfl
67
68
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
^ • GEOTRICHUM Link. Mycelium white, septate; conidiophores absent; conidia (arthrospores) hyaline,
j^ 1-celled, short cylindrical with truncate ends, formed by segmentation of hyphae; mostly saprophytic,
common in soil. Some basidiomycetes form conidia in this manner.
{?'-. Illustration: (A) G. candidum; original, from agar culture; (B) conidial state of Polyporus adust us;
. -V original from culture. Reference (50).
OIDIODENDRON Robak. Mycelium hyaline to brown; conidiophores sparsely branched only on upper
portion, rebranched irregularly, branches segmenting into rod-shaped or rounded conidia, remaining in
chains; conidia (arthrospores) 1-celled, hyaline or subhyaline; saprophytic.
IHustration:0. griseum; original, from culture. (A) branched conidiophore; (B) segmenting branch;
(C) conidia. Reference (15).
AMBLYOSPORIUM Fres. Mycelium pale to yellow-orange; conidiophores erect, septate, lower portion
unbranched. bearing a number of irregular branches near or at the apex, from which conidial chains are
formed by segmentation; conidia (arthrospores) 1-celled, hyaline or yellow-orange in mass, barrel-shaped,
catenulate; saprophytic in soil or often growing on fleshy or woody basidiomycetes.
Illustration: A. spongiosum; original, from culture. (A) conidiophore and conidia; (B) stages in
development of conidial branches; (C) conidia. References (313, 332).
CHRYSOSPORIUM Corda. Conidiophores poorly differentiated, much like vegetative hyphae, mostly
erect and branching irregularly, hyaline; conidia (aleuriospores or arthrospores) hyaline, 1-celled, globose
to pyriform, terminal or intercalary, single or in short chains, usually with a broad basal scar; saprophytic.
Carmichael (51) describes conidia as aleuriospores.
Illustration: Chrysosporium sp.; original from culture. (A) portions of conidiophores and conidia;
(B) conidia. Reference (51).
'
r- OIDIUM Sacc. Mycelium external on host, white; conidiophores upright, simple; upper portion increases
in length as conidia are formed; conidia (meristem arthrospores) cylindrical, 1-celled, hyaline, produced in
basipetal chains; parasitic on higher plants, producing powdery mildews. See Bisby (35) for relation of
Oidium Link., Oidium Sacc. and Acrosporium Nees.
Illustration: O. monilioides (Erysiphe graminis); original, from fresh material. (A, B) mycelium with
conidiophores and conidia; (C) conidia.
,.
•
f
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
GEOTRICHUM
AMBLYOSPORIUM
OIDIUM
69
70
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
SPOROBOLOMYCES K A u y v e r and van Nicl. Cultures usually pink; reproduction principally by
budding (blastospores); some cells producing sterigmata, each bearing an asymmetrical conidium that is
discharged forcibly; saprophytic.
Illustration: S. salmonieolor; original, from culture. (A) hyphae with conidia produced on sterigmata;
(B) budding cells. Reference (45).
ITERSONILIA Derx. Mycelium forming clamp connections; aerial hyphae simple, forming a sterigma
bearing a single conidium (blastospore); conidia asymmetrical, smooth, hyaline, discharged forcibly;
saprophytic or pathogenic on plants.
Illustration: /. perlexans; redrawn from Tubaki (446). (A) mycelium with clamp connections; (B) conidia
and secondary conidia.
BASIPETOSPORA Cole and Kendrick. Conidiophores simple, resembling vegetative hyphae elongating
slightly at apex as conidia are formed; conidia (meristem arthrospores) globose, with truncate base,
hyaline to pale brown, l-celled in simple basipetal chains; saprophytic; B. rubra is conidial state of
Monascus rubra.
Illustration: B. rubra; original from culture. (A) stages in development of chain of conidia; (B) conidia.
Reference (57).
OVULARIOPSIS Pat. and Har. Mycelium and conidiophores as in Oidium; conidia (meristem
arthrospores) l-celled, hyaline, pyriform to clavate, single at apex or sometimes in short chains; imperfect
state of certain powdery mildews.
Illustration: O. erysiphiodes (conidial state of Phyllactinia corulea); redrawn from Salmon (363).
(A) conidiophore bearing single conidium; (B) conidia.
CANDIDA Berkhout. Mycelium, not extensive; conidia (blastophores) hyaline, l-celled, ovoid to fusoid,
forming short chains by budding; produced apically or laterally on mycelium; mostly common
saprophytes; C. albicans is described as causing moniliasis of man; frequently considered as a
filamentous yeast.
Illustration: C. albicans; original, from culture. (A, B) hyphae and conidia; (C) lateral production of
conidia; (D) conidia budding. References (17, 59).
AHJREOBASIDIUM Viola and Boyer. Mycelium not extensive, hyaline when young, becoming dark
with age, black and shiny in old cultures, bearing abundant conidia laterally; conidia (blastospores)
subhyaline to dark, l-celled, ovoid, producing other conidia by budding; saprophytic or weakly parasitic;
common in soil.
Illustration: A. (Pullularla) pullulans; original from culture. (A, B) hyphae and conidia. References
(17, 63).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
^.°o
ITERSONILIA
SPOROBOLOMYCES
A
OVULARIOPSIS
BAS1PETOSPORA
AUREOBASIDIUM
CANDIDA
^F= ^
71
72
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
TILLETIOPSIS Derx. Colonies restricted, white to cream colored, mycelium fine; conidiophores short
or indefinite; conidia (blastospores) 1-celled, hyaline, curved, catenulate, acropetal; common on surface of
leaves; saprophytic, but one species parasitic on powdery mildew. Similar to Sporobolomyces in
appearance.
Illustration: Tilletiopsis sp.; original from culture. Reference (315).
HYALODENDRON Diddens. Mycelium white; conidiophores erect, variable in length, simple or
branched, bearing one to a few conidia at the apex of the branches; conidia (blastospores) frequently in
small clusters, becoming catenulate by acropetalous formation of new conidia, chains often branched,
1-celled, hyaline, variable in shape, ovoid to cylindrical or oblong; saprophytic or parasitic, mostly on
wood; mostly imperfect states of species of Ceratocystis. This genus is like Cladosporium except for lack
of pigmentation.
Illustration: Hyalodendron sp.; original, from culture. (A) conidiophore and conidia; (B) conidia.
References (17, 149).
MONILIA Pers. ex Fr. Mycelium white or gray, abundant in culture; conidiophore branched, its cells
differing little from the older conidia; conidia (blastospores) pink, gray, or tan in mass, I-celled, short
cylindric to rounded, in acropetalous branched chains. Some species are imperfect states of Neuropspora
and are common saprophytes; others, whose perfect states are Molinilia (Sclerotmia) spp., cause brown
rots of fruits.
Illustration: (A) M. (Neurospora) sitophilia; (B) M. americana (Monilinia fructicola); original, from
pure culture.
ZYGOSPORIUM Mont. Conidiophores erect, main'axis usually simple, brown at base with hyaline or
subhyaline apex, bearing special cells (falces), thick-walJed, dark, and reflexed, each bearing 2 short
hyaline conidiogenous cells; conidia (blastospores) 1-celled, hyaline, globose to ellipsoid; saprophytic.
Illustration: Z. masonii; original, from culture. (A) conidiophores showing falces and conidia; (B)
conidia; (C) Z. gibbum; original, from culture. References (188, 462).
DESCRIPTIONS AND liiUSTRATIONS OP GENERA
TILLETIOPSIS
MONILIA
HYALODENDRON
ZYGOSPORIUM
73
74
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
TORULA Pers. Conidiophores short, dark, simple, branched or absent; conidia (porospores, blastospores) 1- to several-celled, cells rounded, dark, in acropetalous chains; saprophytic. Barron (17) describes
conidia as porospores.
Illustration: T. herbarum\ original from culture. Reference (365).
OLPITRICHUM Atkinson. Conidiophores stout, simple or irregularly branched in upper portion;
method of branching irregular, often as extensions of the denticles; denticles medium to long, at nearly
right angles; fertile portions of conidiophore not swollen as in Acladium\ conidia I-celled, hyaline to pale
brown, globose or ovoid to ellipsoid, borne singly on the denticles or branches; saprophytic or parasitic on
other fungi. Relation to Adadium is not clear but separated here because of loose branching and long
"denticles." See Subramanian (409) for his views.
Illustration: O. macrosporum; original, from culture. (A, B) conidiophores and conidia; (C) phialide
state. References (17, 409, 414).
PERICON1A Bon. Conidiophores dark, tall, upright, stout, simple, determinate, somewhat enlarged at
apex, which bears a loose head of comdia; conidia (blastospores) dark, 1-celled, globose, in dry chains,
arising from globose conidiogenous cells; parasitic or saprophytic.
Illustration: Periconia sp.; original from fresh material on dead stem. (A) group of conidiophores; (B)
conidiophore enlarged; (C) tip of conidiophores bearing conidia; (D) conidium. References (282, 401).
CRISTULARIELLA Hochn. Conidiophore-like structures hyaline, consisting of basal stalk and much
branched upper portion that forms a globose or pyramidial head; branches compact and dichotomously
or trichotomously rebranched; cells irregular, thick; conidia not produced, although ultimate cells
resemble conidia; entire structure disseminated as a propagule; small phialides and microconidia produced
in culture, as well as large black sclerotia; causing targetlike spots on living leaves. Niedbalski et al. (314)
consider the entire branched structure as a conidium.
Illustration: (A-C, E) C. pyramidalis; (D), C. depraedans: original from fresh material on Acer leaves; (E),
microconidia from culture. References (352, 464).
ARTHRINIUM Kunze ex. Fr. Conidiophore mother cells subspherical; conidiophores simple, mostly
hyaline except for thick dark septa, increasing in length near base; conidia (meristem blastospores) dark,
1-celled, broadly fusoid, ovoid, curved to cuspidate, attached on side and apex of conidiophore, often with
slight germ slit on one side; saprophytic on plant material.
Illustration: (A-C) A. cuspidatum; (A) cluster of conidiophores; (B) conidiophores and conidia; (C)
conidia; (D) A. aphaerospermum, showing basal conidiophore mother cell; redrawn from Ellis (120).
References (62, 118, 120, 125).
DESCRIPTIONS AND ILLUSTRATIONS OP GENERA
OLPITRICHUM
TORULA
PERICONIA
CRISTULARIELLA
Q
ARTHRINIUM
75
76
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
^
S* BOTRVTIS Pers. Conidiophores tall, slender, determinate, hyaline or pigmented, branched irregularly in
_. upper portion, apical cells enlarged or rounded, bearing clusters of conidia simultaneously on short
Aj&cnticles; conidia (botryoblastospores) hyaline or gray in mass, [-celled, ovoid; black irregular sclerotia
often present; causing "gray mold" on many plants or saprophytic. See Hennebert (167) for recent
classification.
Illustration: B. cinerea; original from culture. (A, B) conidiophores and conidia; (C, D) upper portion of
conidiophore showing enlarged conidiogenous cells; (E) conidia. References { 1 7 , 1 6 7 , 294, 295).
OEDOCEPHALUM Preuss. Conidiophores simple, hyaline, enlarged and globose at the apex, bearing a
head of dry conidia formed simultaneously; conidia (botryoblastospores) hyaline, 1-celled, globose to
ovoid; usually saprophytic on plant materials or in soil. Some species are conidial states of Discomycetes
and one species is the conidial state of Fames annosus.
Illustration: Oedocephalum sp.; original, from culture. (A) conidophores and conidial heads;
(B) enlarged apex of conidiophore void of conidia; (C) conidia. References (17, 427, 448).
BOTRYOSPORIUM Corda. Conidiophores tall, slender, hyaline, composed of elongated axis and
numerous, lateral branches of nearly equal length, these branches producing two or more secondary
branches that are enlarged at the tips and bear heads of conidia; conidia (botryoblastospores) hyaline,
1-celled, ovoid; saprophytic on decaying plant material.
Illustration: Botryosporium sp.; original, from decayed leaf in greenhouse. (A) entire conidiophore;
(B-F) stages in development of conidiophore branch and production of conidia; (G) conidia.
Reference (17).
RHINOTRICHUM Corda {Oidium Link). Mycelium often forming a loose or dense substratum;
conidiophores erect or suberect, simple or branched; conidium-bearing cells sometimes enlarged; conidia
(blastospores) 1-celled, globose to ovoid, hyaline or slightly colored, borne on denticles; saprophytic,
mostly on decayed wood. Not Rhinotrkhum Auct.
Illustration: R. curtisii; original, drawn from herbarium material; (A. B) mycelium, conidiophores and
conidia. References (17, 35, 267, 409, 414).
GONATOBOTRYS Corda. Conidiophores erect, sometimes tall, septate, simple or sparingly branched,
percurrent with terminal and intercalary, inflated, denticulate cells bearing conidia simultaneously; conidia
(botryoblastospores) borne singly on the teeth, 1-celled, hyaline, ovoid to subglobose; saprophytic or
parasitic on other fungi. This genus differs from Gonatobotryum in being hyaline throughout, and from
Gonatorrhodiella in having conidia not in chains. G. simplex is a mycoparasite.
Illustration: G. simplex; original, from culture. (A) conidiophore with clusters of conidia; (B) cluster of
conidia; (C) portion of conidiophore void of conidia; (D) conidia. References (17, 469).
ACLADIUM Link ex Pers. Conidiophores stout, simple or irregularly branched in upper portion, often
extending percurrently, resulting in a row of fertile cells; fertile cells irregular, somewhat inflated (not
globose); conidia (blastospores) hyaline to pale brown, 1-celled, globose to ellipsoid, borne singly on short
or medium denticles; saprophytic or closely associated with other fungi. Isolates are variable, some
producing Aspergilius-Wke heads of microconidia. The relationship to Olphrichum Atkinson and
Rhinotrkhum Auct. is not clear.
Illustration: A. teneltum; (A) young conidiophore and conidia; (B) chain of fertile cells with prominent
denticles; (C) phialide state; original, from culture. Reference (409).
DESCRIPTIONS AND I L L U S T R A T I O N S OF GENERA 77
A
B
RHINOTRICHUM
ACLADIUM
78
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
DICHOBOTRYS Hennebert. Conidiophores tall, slender, dichotomously branched twice or more from
upper half, terminal fertile cells somewhat inflated, globose, producing conidia simultaneously, then
collapsing, conidia (botryoblastospores) nearly globose, hyaline, 1-celled, nearly sessile or on
short denticles.
Illustration: D. abundans (conidial state of Trichophaea abundans). (A) upper portion of conidiophore;
(B) cluster of conidia; (C) conidia. Original from culture. Reference (167.)
PHYMATOTRICHUM Bon. Conidiophores rather short, stout, simple or branched, with inflated or
lobed tips, bearing loose heads of dry conidia; conidia (botryoblastospores) hyaline, 1-celled, produced on
mats on surface of soil, globose or ovoid; saprophytic or parasitic on soil, causing root rots; large black
sclerotia produced in soil; branched setae often present on mycelium. Hennebert (167 394, 432) places this
genus in the newly formed genus Phymatotrichopsis.
Illustration: P. omnivorum; redrawn from photographs by J. Baniecki. (A) rope of hyphae; (B)
mycelium, conidiophores and conidia. Reference (6).
GONATOBOTRYUM Sacc. Conidiophores dark, tall, stout, upright, typically simple, septate, forming a
head of dry conidia on an inflated terminal cell, proliferating to form successive conidiogenous nodes;
conidia (botryoblastospores) dark, 1-celled, ovoid to short cylindrical. G. apiculatum bears conidia in
branched chains of several conidia; saprophytic or causing leaf spots of Hamamelis.
Illustration: original, from culture. (A) B. appiculatum, conidiophores and conidia; (B) G. fuscum,
conidiophore and conidia. References (255, 459).
GONATORRHODIELLA Thaxter. Conidiophores stout, upright, hyaline, simple or sparingly branched,
septate, with inflated apex and intercalary cells that bear loose dry heads of conidia; conidia (botryoblastospores) hyaline, 1-celled, ovoid to ellipsoid, in simple or branched acropetalous chains; frequently
associated with Hypoerea, Hypomyces, or Nectria. G highlei is parasitic on TV coccinea varfaginaia, the
cause of beech bark disease in New England.
Illustration: G highlei; original, from culture. (A) conidiophores and conidia; (B) apex of branch
showing denticles; (C) conidia. Other references (138, 437, 459).
LACELLINA Sacc. Setae erect, tall, brown, simple; conidiophores determinate, intermixed with setae,
shorter, pale, simple; conidia (blastospores) 1-celled, globose or ovoid, colored, produced at or near the
apex in acropetalous chains; saprophytic.
Illustration: L. graminkola; (A) habit of setae and conidiophores; (B) tip of seta; (C, D) conidiophores
and conidia; redrawn from Subramanian (396).
LACELLINOPSIS Subramanian. Setae simple, septate, brown; conidiophores determinate intermixed
with setae, with globose fertile apex, becoming cupulate after detachment of conidia; conidia (blastospores) 1-celled, brown, globose, produced acropetally in chains.
Illustration: L sacchari: (A) tip of seta; (B) conidiophores and conidia; (C) mature conidia; redrawn
from Subramanian (397).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
* .;
GONATORRHODIELLA
LACEUINA
LACELUNOPSIS
79
80 DESCRIPTIONS A N D I L L U S T R A T I O N S OF GENERA
CHROMELOSPORIUM Corda. Mycelium white to cinnamon, growing rapidly; conidiophores stout,
hyaline, erect, main axis unbranched but dichotomously branched near apex, producing several clublike
divergent branches that are covered by conidia on slender short denticles; conidia (botryoblastospores)
globose, 1-celled, hyaline or nearly so (tan in mass); saprophytic in soil, common in greenhouses.
Illustration: C. ollare; (Ostracoderma state of Peziza ostracoderma); original, from culture.
(A) conidiophore and conidia; (B) fertile branch with conidia. References (17, 168).
HAPLOGRAPHIUM Berk, and Broome. Mycelium dark; conidiophores determinate dark, simple,
erect, bearing an apical cluster of pale to hyaline short branches, entire apparatus penicillate; conidia
(blastospores) terminal, hyaline, 1-celled, ovoid to oblong, collecting in slimy heads under moist
conditions; saprophytic on wood or soil.
Illustration: Haplographium sp.; original, from fresh material on decaying wood. (A) conidiophores and
conidia; (Q conidia. Reference (17.)
MICROCLAVIA F.S. Stevens. Mycelium superficial; conidiophores simple, determinate, pale, expanded
at apex into an obconical or ellipsoid structure, usually composed of 2 cells, apical cell bearing 2
(sometimes 3) large, brown, 1-celled, thick-walled conidia (aleuriospores), subglobose with flattened base,
rarely deciduous; overgrowing and probably hyperparasitic on microthyriaceous fungi on leaves.
Illustration: M. bispora; redrawn from Deighton (80). (A) conidiophores and conidia; (B) portion
of mycelium.
STAPH YLOTRICHUM Meyer and Nicot. Mycelium hyaline to lightly pigmented; conidiophores erect,
tall, dark brown but paler above, branched irregularly in upper poriton; conidia (aleuriospores) globose,
1-celled, thick-walled, light brown, apical and single on branches; saprophytic.
Illustration: S- coccosporum; original, from culture. References (275, 311).
BLASTOMYCES Cost, and Roll. Mycelium white in culture, filamentous at room temperature, yeastlike
at 37 °C; conidia (aleuriospores) thick-walled, budding cells (blastospores) found in lesions; pathogenic in
man, causing blastomycosis.
Illustration: H. dermatitidis; (A) hyphae and thick-walled cells (aleuriospores) produced in culture; (B)
bud-cells produced in tissue; (C) budding cells on media at 37 °C. (A, B) redrawn from DeLamater (86);
(C) drawn from a photography by Salvin (364). Other references (59, 129).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
»
CHROMELOSPORIUM
MICROCLAVIA
HAPLOGRAPHIUM
^P <3
<s
STAPHYLOTR1CHUM
BLASTOMYCES
81
82 DESCRIPTIONS AND I L L U S T R A T I O N S OF GENERA
STEPHANOMA Wallr. Conidiophores slender, hyaline; conidia (aleuriospores) apical on pedicels,
hyaline or brown, main cell large, globose, with several cell-like hyaline swellings; phialospore state may
be present, with verticillate conidiophores bearing hyaline, I-celled conidia (Verticillium-like); parasitic on
other fungi; may be imperfect state of Hypomyces. The outgrowths on the aleuriospores separate this
genus from Sepedonium. S. phaeospora has brown conidia, and is a biotophic mycoparasite.
Illustration: S. tetracoccum; (A) hyphae and aleuriospores; (B) conidiophore and phialides; redrawn
from Howell (178). References (46, 452).
MYCOGONE Link. Conidiophores much like branches of mycelium, simple or branched; conidia
(aleuriospores) single, apical, hyaline or brightly colored, 2-celled, the apical cell globose and warted, basal
cell smooth; phialospore state may also be present, hyaline, 1-celled Vertitillium-like; parasitic on
mushrooms, probably imperfect state of Hypomyces.
Illustration: M. perniciosa; (A) conidiophore and phialides; (B) hyphae and aleuriospores; redrawn from
Howell (178). Reference (17.)
SEPEDONIUM Link. Conidiophores indefinite, not differing much from branches of the mycelium,
simple or branched; conidia (aleuriospores) single or in loose cluster, hyaline or bright yellow, globose,
1-celled, tuberculate; parasitic on fleshy fungi; a Verticillium-Yike state is usually also present; imperfect
states of Hypomyces. Two species illustrated are similar except for the verticillate conidial state.
Illustration: S. ampullosporum\ original, from culture; (A) verticillate conidiophore and conidia;
(B) aleuriospores; (C) S. chrysospermum\ original, from culture. References (17, 72).
HISTOPLASMA Darling. Cultures similar to Blastomyces but large, thick-walled, tuberculate, spherical
aleuriospores formed in culture at room temperature; growth yeastlike, at 37 °C; pathogenic in man,
causing histoplasmosis.
Illustration: H. capsulatum. (A) hyphae and tuberculate conidia; (B) stages in the development of
tuberculate aleuriospores; (C) smooth-walled conidia developed below the surface of the agar; redrawn
from Howell (178). Other reference (129).
CHLAMYDOMYCES Bain. Conidiophores much like mycelium; conidia borne on slender branches;
conidia (aleuriospores) 2-celled, with large tuberculate apical cell and small, smooth wedge-shaped basal
cell, hyaline or slightly colored; phialospore state also produced, small, hyaline, 1-celled, borne on short
phialides on swollen head; parasitic on mushrooms, probably imperfect state of Hypomyces. Compare
with Mycogone,
NIGROSPORA Zimm. Conidiophores short, mostly simple; conidia (aleuriospores) shiny black,
1-celled, globose, situated on a flattened, hyaline vesicle (cell) at the end of the conidiophore; parasitic on
plants or saprophytic.
Illustration: J V . sphaerica; original. (A, B) conidiophores and conidia; (C) tip of conidophore showing
hyaline vesicle; (B, C) from culture. References (17, 180)
PAPULARIA Fr. Conidiophores poorly developed in culture, mostly simple, hyaline, short branches of
mycelium, conidia (blastophores may appear to be aleuriospores in culture) I-celled, dark, ovoid, broadly
lenticular or globose, often with a light band seen in side view; saprophytic. Compare with Arthrinium
and see Ellis (120) for synonymy.
Illustration: Papularia sp.; original, from culture. References (124, 125).
DESCRIPTIONS AND ILLUSTRATIONS OF GENtRA
STEPHANOMA
LawO
SEPEDONIUM
HISTOPLASMA
N1GR0SP0RA
PAPULARIA
83
84 DESCRIPTIONS A N D I L L U S T R A T I O N S OF GENERA
ASTEROMYCES Moreau. Hyphae hyaline to brown; conidiogenous cells sessile or with short stalk,
dark, inflated as conidia are formed; conidia (aleuriospores) 1-celled, dark, clustered, borne on long
denticles, obclavate to pyriform; saprophytic.
IHustration: A. cruciatus; redrawn from Hennebert (164). (A) mycelium with short conidiophores;
(B) conidiophores and conidia. Redrawn by permission of the National Research Council of Canada from
the Canadian Journal of Botany, 40, pp. 1203-1216 (1962).
MAMMARIA Cesati. Conidiophores erect or repent, often much like vegetative hyphae, simple or
bearing very short branches, pale brown; conidia (aleuriospores) borne directly on aerial hyphae or on
conidiophores, 1-celled, dark, ovoid to pointed, truncate at basal scar, with prominent longitudinal germ
slit, in groups or clusters; saprophytic.
Illustration: M. echinobotryoides; redrawn from Hennebert (17, 166). (A) conidiophores and conidia;
(B) mycelium bearing two types of conidia.
HUMICOLA Traaen. Conidiophores, simple or rarely with short branches, dark; conidia (aleuriospores)
single, apical, globose or subglobose, brown, 1-celled; some species also produce simple phialides and
phialospores in chains; saprophytic.
Illustration: H.fuscoatra; original, from culture. (A) conidiophores and conidia; (B) phialides and chains
of small conidia. References (64,471).
BOTRYOTRICHUM Sacc. and March. Setae in loose tufts, simple, gray to grown; conidiophores short,
irregularly branched, hyaline, bearing a loose cluster of conidia; conidia (aleuriospores) 1-celled, brown,
borne singly, globose; saprophytic, frequently in soil. B. piluliferum also produces simple phialides and
hyaline, I-celled phialospores, in chains.
Illustration; B. piluliferm; original, from culture. (A) conidiophores with aleuriospores; (B) philiades with
phailospores; (C) seta. References (75, 95).
WARDOMYCES Brooks and Hansford. Conidiophores, hyaline, short, branched repeatedly; conidia
(aleuriospores) 1-eelled, brown to black, ovoid to ellipsoid, produced singly at apices of branches;
saprophytic.
Illustration: W. anomala; original, from culture. (A) mycelium producing conidia; (B) conidiophores and
conidia; (C) conidia. References (40, 91, 164, 166).
EC HI NOB OTR YUM Corda. Conidiophores consisting of short, branched, undifferentiated hyphae, or
nearly absent; conidia (aleuriospores) ovoid or somewhat flask-shaped, tapering to a pointed apex,
smooth or rough, formed in clusters at hyphal tips, dark, 1-celled.
Illustration: E. atrum; original, from culture. Reference (166).
GILMANIELLA Barron. Conidiophores hyaline, short, often stout to inflated, mostly simple; conidia
(aleuriospores) apical, single, dark brown or black, 1-celled, globose, with a thick wall, wall smooth or
rough, with a prominent germ pore; saprophytic on wood or soil.
Illustration: Gilmaniella sp. Original, from decayed wood and from culture. (A) conidiophores and
conidia; (B) stages in development of conidiophore and conidium; (C) mature conidia showing germ pore.
Reference (16).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
ECHINOBOTRYUM
85
86
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
GLOMERULARIA Peck. Conidiophores borne in groups in spots on living leaves, mostly short,
hyaline, simple or divided; conidia (aleuriospores) globose, somewhat unequally clustered forming
few-spored heads, 1-ceiled, hyaline; parasitic on leaves.
Illustration: G. corni; original, from herbarium material on leaves of Cornus canadensis. (A) habit on
leaf; (B) conidiophores and conidia.
BOTRYODERMA Papendorf and Upadhyay. Mycelium hyaline; conidiophores short, hyaline, variable,
sometimes missing; conidiogenous eells subglobose or obpyriform; conidia (aleuriospores) terminal or
lateral, sessile or on short sterigmata, I-cclled, broadly ellipsoid to globose, hyaline, smooth, often with
prominent scar; saprophytic in soil.
Illustration: B. lateritium; redrawn from Papendorf and Upadhyay (321). (A) mycelium and branched
conidiophores; (B) conidia.
UMBELOPSIS Amos and Barnett. Conidiophores hyaline, often septate, older conidiophores typically
with a swollen apex bearing 2 to several long cylindrical branches, each with a single apical conidium;
conidia (aleuriospores) I-celled, hyaline, globose; saprophytic in soil. This fungus may prove to be a
Mortierella, but because of its similarity to the imperfects it is included here.
Illustration: U. versiformis: original, from culture. (A-D) stages in development of conidiophores and
conidia. References (2, 17).
MONILOCHAETES Halst. Conidiophores dark, erect, slender, usually simple, septate; conidia (phialospores) hyaline or becoming pigmented in age, borne singly at the apex or produced in chains under
conditions of high humidity; parasitic.
Illustration: M. infuscans; (A, C) conidiophores and conidia on sweet potato; (B, C) conidiophores and
conidia produced in culture. (A, B) redrawn from Harter (160). (C, D) redrawn from Taubenhaus (431).
MONOCILLIUM Saksena. Conidiophores simple, septate, consisting of a pedicel and a swollen vesicle
terminating in a single phialide that bears a long chain of conidia formed basipetally; conidia
(phialospores) i-celled, hyaline, ovoid to ellipsoid, smooth; saprophytic, from soil.
Illustration: M. indicum; redrawm from Saskena (362). (A) mycelial rope bearing conidiophores;
(B) conidiophore and conidia.
GLIOMASTIX Gueg. Mycelium hyaline to dark, forming aerial"ropes" in culture; conidiophores mostly
reduced to simple phialides, hyaline or dark, slender, tapering toward the apex; conidia (phialospores)
dark, 1-celled, globose to ovoid to ellipsoid, formed in basipetal chains without slime or aggregated in
slime droplets; saprophytic.
Illustration: G. murorum; original, from culture. (A) mycelial rope; (B) conidiophores (phialides); (C)
conidia. References (42, 92).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
GL10MASTIX
MONOCILLIUM
87
88 DESCRIPTIONS AND I L L U S T R A T I O N S OF GENERA
PHIALOPHORA Medlar. Conidiophores short or reduced to phialides, dark, simple or branched;
phialides cylindrical to inflated, often with flaring collarette at apex; conidia (phialospores) subhyaline to
dark, 1-celled, globose to ovoid, extruding from phialide in moist heads; parasitic or saprophytic. The
genus Margarinomyces is often included under Phialophora,
Illustration: (A-C) Phialophora sp.; original, from culture. (A) rope of mycelium with slime heads of
conidia; (B) conidophores (phialides); (C) conidia; (D, E) Phialophora sp. (Margarinomyces bubaki);
original, from culture. (D) mycelium bearing phialides; (E) conidia. References (47, 312, 461, 140).
CHLORIDIUM Link. (Bisporomyces van Beyma). Conidiophores erect, simple, septate, dark, frequently
proliferating at the apex after producing an apical head of conidia, with a distinct collarette at apex;
conidia (phialospores) 1-celled, hyaline, frequently in pairs at the end of the conidiophore or held together
in small heads by mucus; aleuriospores (where present) 1-celled, terminal; saprophytic, on decaying wood.
Illustration: C. chlamydosporis; original, from culture. (A) group of conidiophores with slime heads; (B)
conidiophores with slime heads; (B) conidiophores and conidia; (C) conidia; (D) aleuriospores. References
(280,281,318,452).
MENISPORA Pers. Setae (if present) straight, bent or coiled; conidiophores dark, simple, or branched;
phialides slender, somewhat curved with an inconspicuous collarette; conidia (phialospores) hyaline,
I-celled (sometimes septate), borne apically in slimy masses, narrowly fusiform to curved; conidia of some
species have a slender hyaline appendage at each end; saprophytic.
Illustration: (A) M. cobaltina; original, from herbarium material on dead leaves of Nyssa; conidiophores
and conidia; (B) M. ciliate; original, from culture; conidiophore and ciliate conidia. References (174, 215).
STACHYBOTRYS Corda. Conidiophores subhyaline to dark, simple, determinate bearing at apex a
cluster of thick, short phialides; conidia (phialospores) dark, 1-celled, globose to ovoid, borne in moist
heads at the apex of the phialides, not catenulate; saprophytic.
Illustration: S. atra; original, from culture isolated from soil. (A) habit sketch; (B, C) conidiophores and
clusters of conidia; (D) conidia. References (33, 34, 480).
CODINAEA Maire (MENISPORELLA Agnihothrudu). Setae straight or slightly bent, thick-walled, dark,
independent or a sterile portion of conidiophore; phialides mostly terminal, straight, sometimes
proliferating, forming conspicuous collarettes that are cupulate, or funnel-shaped, flaring; conidia
(phialospores) hyaline, 1-celled (sometimes to 4-celled), with a slender seta at each end; saprophytic on
plant material or soil.
Illustration: Codinaea sp.; original, from fresh material on over-wintered acorn. (A) conidiophores
showing collarette; (B) ciliate conidia. Reference (17).
MEMNONIELLA Hohn. Conidiophores dark, simple, bearing at apex a cluster of thick, short phialides;
conidia (phialospores) dark, I-cellcd, globose, catenulate; saprophytic; probably closely related
to Stachybotrys.
Illustration: Memnoniella sp.; drawn from photography by Zuck (480). Reference (34).
DESCRIPTIONS AND ILLUSTRATIONS OF GENfcRA
. -.<>#.*
c
0O
COOINAEA
89
90
DESCRIPTIONS AND ILLUSTRATIONS OF GENFRA
CIRCINOTRICHUM Nees ex Persoon. Hyphae subhyaline to brown, bearing setae and phialides; setae
simple, erect, verrucose, dark, brown, wider at base and tapering toward apex that is paler and circinate;
phialides short, obclavate, hyaline or subhyaline, arising from superficial mycelium; conidia (phialospores)
hyaline, (-celled, narrowly ellipsoid, straight or curved, aggregated into apical clusters. Saprophytic on
leaves or twigs. Compare with Gyrothrix.
Illustration: C. maculiforme; redrawn from Pirozynski (330). (A) seta; (B) phialides and conidia.
CYROTHKIX (Corda) Corda. Mycelium subhyaline to brown; setae erect, repeatedly branched, straight
or flexuous, pale to brown, broader and darker at the base; arising from the mycelium, obclavate, hyaline;
conidia (phialospores) hyaline, 1-celled, narrowly ellipsoid, straight or curved, often aggregated. Compare
with Circinotrkhum. Saprophytic on leaves and twigs.
Illustration: G. circinata; redrawn from Piro/ynski (330). (A) branched seta; (B) phialides and conidia.
CHALARA Corda. Mycelium typically dark; conidiophore typically has some dark pigment but may be
hyaline under some cultural conditions, unicellular or basal portion septate, the apical cell (phialide)
sometimes tapering upward slightly and producing conidia endogenously; conidia (phialospores) hyaline,
cylindrical, somewhat variable in length, often hanging together in chains; parasitic or saprophytic.
Illustration: (A) C. quercina (Ceratocystis fagacearum); original, from pure culture; conidiophores and
conidia; (B-D) Chaiara sp.; original, from fresh material on rotted wood; (B) habit of conidiophores; (C)
enlarged conidiophore showing deep collarette; (D) chain of conidia. References (17, 169).
CHAETOCHALARA Sutton and Pirozynski. Mycelium partly immersed in leaves, emerging through
stomata, giving rise directly to brown, simple, pointed setae and to hyaline to brown phialides; phialides
cylindrical with swollen rounded base; conidia (phialospores) 1- to 2-celled, hyaline, cylindrical, in chains;
saprophytic on leaves.
Illustration: C. cladii; redrawn from Sutton and Pirozynski (427). (A) phialides and seta; (B) enlarged
phialide; (C) conidia.
CHALAROPSIS Peyron. Conidiophores usually pigmented or subhyaline, slender phialides slightly
larger near the base and tapering upward; producing conidia endogenously; conidia (phialospores)
hyaline, cylindrical, often in chains; aleuriospores present, ovoid, dark, thick-walled, single or in short
chains; parasitic or saprophytic; similar to Chaiara except for the production of aleuriospores.
Illustration: Chalaropsis sp.; original from pure culture. (A) hyphae producing aleuriospores; (B) conidia
and phialide.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
GYROTHRIX
CHAETOCHALARA
^
1
o
CHALARA
CHAIAROPSIS
91
92
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
THIELAVIOPSIS Wctn. Conidiophores, phialides and phialospores like Chalaropsis: also forming thickwalled aleuriospores that eventually break apart; parasitic or saprophytic; conidial states of species of
Ceratocystis.
Illustration: T. basicola, original, from culture. (A) phialide and phialospores; (B) chains of aleuriospores;
(C) hyphae producing both kinds of spores.
GLIOCLADIUM Corda. Conidiophores hyaline, the upper portion bearing penicillate branches, forming a
compact "brush" as in Penicillium; conidia (phialospores) hyaline or brightly colored in mass, 1-celled,
produced successively apically and collecting in mucilaginous droplets; saprophytic, common in soil. G.
roseum also produced a Verticillium state. See VertiriUium figure D.
Illustration: G. deliquescens; original, from culture isolated from soil. (A) conidiophores and heads of
conidia as seen in dry mount; (B) conidiophores and conidia in water. References {298, 350, 379).
^VERTICILLIUM Nees. Conidiophores slender, branched, at least some of the branches or phialides
f^ verticillate, conidia (phialospores) ovoid to ellipsoid, hyaline, 1-celled, borne singly or in small moist
,^>*' clusters apically; vascular parasites causing wilts on higher plants, parasitic on other fungi, or growing
,
saprophytically. Also see Verticillium states of Gliocladium roseum, Stilbum, Sepedonium, Mycogone,
Y
Stephanoma, etc.
> jC
'
s\f
Illustration: V. albo-atrum; original, from pure culture. (A) conidiophores growing in moist atmosphere;
(B) conidiophore in water mount; (C) conidia; (D) Verticillium state of Gliocladium roseum. References
(44,236,237,359).
STACHYLIDIUM Link. Conidiophores dark, upright, slender, upper portion branched bearing whorls
of phialides; conidia (phialospores) subhyaline to brown, 1-celled, ovoid, small, held in heads by slime;
saprophytic on vegetable material.
Illustration: Stachylidium sp.; original from culture. (A) branched conidiophore; (B) phialides with
heads of conidia. References (125, 193).
TRICHODERMA Pers. Conidiophores hyaline, much branched, not verticillate; phialides single or in
groups; conidia (phialospores) hyaline, 1-celled, ovoid, borne in small terminal clusters; usually easily
recognized by its rapid growth and green patches or cushions of conidia; saprophytic on soil or on wood,
very common, some species reported as parasites on other fungi.
Illustration: T. viride; original, from pure culture. (A, B) large conidiophores showing extensive
branching; (C, D) phialides showing production of conidia; (E) conidia. Reference (354).
CLADOSPOR1ELLA Deighton. Mycelium slow-growing, dark in culture, conidiophores simple, length
variable, pale olive to pale brown, with distinct conidial scars; conidia (sympodulospores) catenulate,
acropetal, variable, long-cylindrical to filiform, 1- to several-celled, pale olive-brown, associated with and
possibly parasitic on Cercospora,
Illustration: C. cercosporicola; original from culture.
WALLEMIA .lohan-Olsen. Colonies small, slow-growing, orange-brown to dark brown; conidiophores
closely clustered, simple, with phialidelike lower portion with dark collarette, sometimes proliferating
percurrcntly, base often somewhat swollen; conidiogenous cell protruding, cylindrical, becoming septate
and fragmenting to form arthrospores; conidia subhyaline to brown in mass, 1-celled, becoming globose.
Illustration: W. seba; original from culture. References (17, 276).
DESCRIPTIONS AND ILLUSTRATIONS Of GENFRA
93
94
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
PAECILOMYCES Bainer. Conidiophores and branches more divergent than in Penicillium; conidia
(phialospores) in dry basipetal chains, 1-celled, ovoid to fusoid, hyaline; saprophytic.
Illustration: Paecilomyces sp.; original, from culture. (A) conidiophores with chains of conidia;
(B) conidia. References (41, 319).
PENICILLIUM Link. Conidiophores arising from the mycelium singly or less often in synnemata,
branched near the apex, penicillate, ending in a group of phialides; conidia (phialospores) hyaline or
brightly colored in mass, 1-celled, mostly globose or ovoid, in dry basipetal chains.
Illustration: Penicillium sp.; original, from culture. (A, B, C) types of conidiophores; (D) branches,
phialides, and chains of conidia. References (349).
ASPERGILLUS Link. Conidiophores upright, simple, terminating in a globose or clavate swelling,
bearing phialides at the apex or radiating from the apex or the entire surface; conidia (phialospores)
1-celled, globose, often variously colored in mass, in dry basipetal chains.
Illustration: Aspergillus spp.; original, from culture. (A) habit sketch; (B, C) conidiophores with conidial
heads. References (349).
PHIALOM YCES Misra and Talbot. Conidiophores tall, slender, hyaline, simple or sparingly branched, a
single apical whorl of phialides; conidia (phialospores) 1-celled, dark, lemon-shaped, verrucose, in dry
basipetal chains; saprophytic from soil.
Illustration: P. macrosporus; redrawn from Misra and Talbot (288). Redrawn by permission of the
National Research Council of Canada from the Canadian Journal of Botany, 42, pp. 1287-1290 (1964).
METARRHIZIUM Sorok. Conidiophores hyaline, branched, forming a sporulating layer; phialides
single, in pairs, or in whorls; conidia (phialospores) produced in basipetal chains, compacted into columns,
long-ovoid to cylindrical, 1-celled, hyaline or slightly pigmented, olive-green in mass; parasitic on insects,
or saprophytic in soil. Compare with Myrothecium.
Illustration: M. anisoplae; original, from culture. (A) sporulating fungus on insect larva;
(B, C) conidiophores; (D) conidia. References (325).
GLIOCEPHALIS Matruchot. This genus is much like Gftocephahtrichum, but without sterile arms.
Illustration: Gliocephalis sp.; original, diagrammatic. (A) conidiophore and slime head; (B) phialides and
conidia. Reference (128).
CEPHALOSPORIUM Corda. Conidiophore and phialides slender, mostly simple; conidia (phialospores) hyaline, 1-celled, collecting in a slime drop; saprophytic or parasitic, some species causing vascular
wilts of trees. Microconidia of certain species of Fusarium are similar.
Illustration: Cephalosporium sp.; (A) conidiophores and conidia in slime heads; (B, C) phialides; (D)
conidia; original from culture. References (108, 139, 329).
GLIOCEPHALOTRICHUM Ellis and Hesseltine. Conidiophores tall, simple, stout, bearing at the apex
a series of primary and secondary branches that terminate in phialides; fertile area subtended by a few
long sterile divergent arms; conidia (phialospores) hyaline, 1-celled, oblong-elliptical, in moist heads;
saprophytic.
Illustration: G. bulbilium; original from culture. (A, B) conidiophores; (C) phialides; (D) conidia.
References (17, 111).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
GLIOCEPHALOTRICHUM
95
96
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
CHAETOPSINA Rambelli. Conidiophores erect, stout, thick-walled, septate, sometimes swollen at the
base, tapering upward to a sterile point; branches with phialides arising about the middle or lower portion
of conidiophore; phialides in more or less compact layer, inflated below and tapering upward with a long
neck; conidia (phialospores) hyaline, 1-celled, oblong-cylindrical, held in a droplet of slime around the axis
of the conidiophore; saprophytic.
Illustration: C. fulva; original, from culture. (A) habit of conidiophores and spines. (B) enlarged
conidiophore showing phialides and sterile tip; (C) enlarged phialides; (D) conidia. Reference (17).
THYSANOPHORA Kendrick. Conidiophores dark brown, single or clustered, bearing one to several
penicilli on a single stipe, proliferating sympodially after producing a cluster of phialides, otherwise simple
and ascending; 1-celled, subhyaline to pale brown, dry, in basipetal chains, subglobose to elongate fusoid,
minutely roughened; saprophytic.
Illustration: T. longispora redrawn from Kendrick (248). (A) portion of conidiophore bearing phialides
and chains of conidia; (B) conidia. Redrawn by permission of the National Research Council of Canada
from the Canadian Journal of Botany 39, pp. 817-832 (1961).
CHAETOPSIS Grev. Conidiophores dark, long, main axis slender with long sterile apex, bearing
numerous primary side branches and secondary branches (phialides) that elongate and form polyphialides;
conidia (phialospores) hyaline or subhyaline, 2-celled, small cylindrical, sticking together in bundles by
means of slime; saprophytic on wood and bark.
Illustration: C. griseus; (A) group of conidiophores; (B) conidiophore and conidia; redrawn from Hughes
(93, 193).
PHIALOCEPHALA Kendrick. Conidiophores dark, mostly solitary, with a single stipe bearing an
apical, complex fertile head, composed of 3 or 4 series of branches; apical phialides with conspicuous
collarettes; conidia (phialospores) hyaline, 1-celled, globose to cylindrical, aggregate into a large head
in slime.
Illustration: P. bactrospora; original, from culture. (A) habit of conidiophores; (B) mycelium with short
conidiophores; (C) portion of tall conidiophore; (D) enlarged phialides; (E) conidia. Reference (249).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
THYSANOPHORA
CHAETOPSINA
CHAETOPSIS
PHIALOCEPHALA
97
98
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
GONYTRICHUM Nees. Conidiophores dark, mostly tall, slender, sometimes terminating in a long,
slender sterile tip; phialides borne in groups on short lateral branches along main axis of conidiophore,
tapering and often curved; conidia (phialospores) hyaline or subhyaline, ovoid, collecting in small heads;
saprophytic.
Illustration: S. macrodadium; original, from culture, isolated from soil. (A) conidiophores and conidia,
on a dry mount; (B) short simple conidiophores; (C) branch of conidiophore and phialides. Reference (193).
LEPTOGRAPHIUM Lagerb and Melin. Conidiophores upright, single or in clusters, branched, the
upper portion with penicillate branches; lower portion dark but variable in shade, upper branches hyaline;
conidiogenous cells slender; conidia (anellospores) hyaline, ovoid, held together in rather large heads by
slime; parasitic on trees or saprophytic. Probably conidial state of Ceratocystis.
Illustration: Leptographium sp.; original, from culture. (A) habit of conidiophores; (B) conidiophores
bearing conidia; (C) conidiogenous cells showing annellations; (D) conidia. References (77, 148, 369).
SPOROTHRlX Hektoen and Perkins. Conidiophores mostly simple, 1-celled or septate, hyaline, bearing
a loose cluster of dry conidia at apex; conidia (sympodulospores) hyaline, 1-celled, globose to ovoid, borne
on short, prominent denticles; mostly saprophytic. S. schenckii (Sporotrichum schenckii) causes
sporotrichosis in humans.
Illustration: Sporothrix sp.; original, from culture. (A) conidiophores showing denticles and conidia;
(B) conidia. References (17,129).
HANSFORDIA Hughes. Conidiophores hyaline or pigmented, erect to repent, branched above
repeatedly and irregularly; conidiogenous cells elongated, bearing conidia near the apex on blunt
denticles; new growing points arising sympodially; conidia (sympodulospores) 1-celled, hyaline, globose,
ovoid or fusoid; saprophytic on leaves.
Illustration: Hansfordia sp.; original, from culture. (A) conidiophores bearing conidia; (B) conidia.
Reference (187).
SCOPULARIOPSIS Bain. Conidiophores mostly branched or producing at the apex a cluster of conidiogenous cells that proliferate percurrently before producing succeeding conidia, leaving annellations at the
tip; conidia (annelospores) hyaline or subhyaline, 1-celled, globose with a truncate base, produced in
basipetal chains; colonies other than green or blue; saprophytic in soil.
Illustration: Scopulariopsis sp.; original, from culture. (A) portion of conidiophore bearing conidia in
chains; (B) conidiogenous cells showing annellations; (C) conidia. References (303).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
GONYTRICHUM
LEPTOGRAPHIUM
SPOROTHRIX
^
a
0 Oo
SCOPULARIOPSIS
HANSFORD) A
99
100 DESCRIPTIONS A N D I L L U S T R A T I O N S OF G E N E R A
NODULOSPORIUM Preuss. Conidiophores erect or suberect, branched, hyaline to pigmented;
conidiogenous cells slender or short and thick, attached irregularly or verticillatcly, bearing conidia
apically, in succession on new denticles; conidia (sympodulospores) l-celled, hyaline or subhyaline to
distinctly pigmented; saprophytic on wood, conidial states of Xylariaceae.
Illustration: Nodulosporium spp.; original, from culture. (A) conidiophores and conidia of Hypoxylon .
sp.; (B, C) conidiophores and conidia of Hypoxylon atropunctatum. References (242, 357).
BEAUVERIA Vuill. Mycelium white or slightly colored with a white fluffy to powdery appearance;
conidiophores single, irregularly grouped or in vcrticillatc clusters; in some species inflated at the base,
tapering to a slender fertile portion that appears zigzag after several conidia are produced; conidia
(sympodulospores) hyaline, rounded to ovoid, l-celled, dry, borne singly on small denticles; parasitic on
insects.
Illustration: B. bassiana; original, from culture obtained from dead Nitidulid beetle. (A) infected beetle;
(B, C, D) clusters on conidiophores; (E) single conidiophores; (F) conidia. References (21, 274).
BASIDIOBOTRYS Hohn. Conidiophores dark to subhyaline, elongate-clavate, simple, with an enlarged
globose or clavate apex; conidia (sympodulospores) hyaline, fusoid, l-celled, produced on tiny denticles
on short thick conidiogenous cells that cover the apex of conidiophore; caused sapwood rot of hardwood
trees; conidial state of Hypoxylon spp. Jong and Rogers suggest that this fungus should be placed in
Xylocladium Syd.
Illustration: Basidiohotrys sp. (Conidial stage of Hypoxolon punctulatum); original, from culture isolated
from oak wood. (A-C) conidiophores and heads of conidia; (D) conidia; (E) sporogenous cells showing
development of conidia. Reference (7, 242, 243).
TRITIRACHIUM Limber. Conidiophores upright, long, slender, simple or verticil lately branched,
conidiogenous branches tapering to a rachislike, zigzag, fertile portion; conidia (sympodulospores) apical
on new growing points, hyaline, l-celled, globose or ovoid, saprophytic. Note similarity to Beauveria.
Illustration: T. album; original from culture. Reference (274).
VIRGARIA Nees. Conidiophores erect, simple or forked, or scantily upright-branched, septate, dark;
conidia (sympodulospores) apical on sympodially formed new growing points, globose or ovoid,
asymmetrical, l-celled, dark; saprophytic.
Illustration: (A) V. nigra; from herbarium material on bark of Betula; (B) Virgaria sp.; from culture; both
original. Reference (404).
GENICULOSPORIUM Chesters and Greenhalgh. Conidiophores erect, branched, slender, branches
originating from lower portion and giving a subdichotomous appearance, with main axis becoming
indistinct; apical region of branches bearing conidia on new sympodial growing points, giving a geniculate
appearance; conidia (sympodulospores) hyaline to subhyaline, l-celled, ovoid to obovoid with truncate
base; imperfect state of Hypoxylon.
Illustration: G. serpens; redrawn from Chesters and Greenhalgh (53). (A) conidiophores; (B) conidia.
Reference (243).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
GENICULOSPORIUM
VIRGARIA
101
102
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
CONOPEEA Pers. ex Mcrat. (Streptothrix Corda). Mycelium dark, growing loosely on decaying
vegetation; conidiophores erect, tall, branched, branches spirally coiled (appearing wavy); conidia
(sympodulospores) single, apical or lateral, sessile or on short peglike structures, 1-celled, dark;
saprophytic.
Illustration: Canopied sp.; original, from herbarium material on wood. (A) branched conidiophore;
(B) branches with conidia; (C) conidia.
1DRIELLA Nelson and Welhclm. Mycelium hyaline to brown; conidiophores brown, simple, nonseptate,
narrowed above, with prominent scars; conidia (sympodulospores) lunate to falcate, with pointed ends,
produced in clusters near the apex of the conidiophore; aleuriospores brown, several-celled; believed to be
parasitic on strawberry roots.
Illustration: /. lunata; drawn from photographs by Nelson and Wilhelm (307). (A) apex of conidiophore
bearing conidia; (B) conidiophore with detached conidia; (C) chlamydospore.
CALCARISPORIUM Preuss. Conidiophores hyaline, slender, the larger ones verticillately branched,
primary branches usually become slender conidiogenous cells; conidia (sympodulospores) hyaline, 1celled, mostly oblong, borne singly on wartlike teeth on apical portions of the conidiophore branches,
forming loose cluster; principally parasitic on other fungi.
Illustration: (A-C) C. arbwscula; original, from culture. (A) branched conidiophore with clusters of
conidia; (B) branches with apical denticles; (C) conidia. (D-F) C. parasiticum; original, from culture. (D)
tall conidiophore; (D) conidiogenous cell with cluster of conidia; (F) conidiogenous cell showing blunt
denticles. References (8, 1 8 7 , 465, 466).
SELENOSPORELLA Arnaud. Conidiophores brown, pale toward the apex, tall, branched, bearing
several groups of conidiogenous cells verticillately; conidiogenous cells slender, new growing points
formed sympodially; conidia (sympodulospores) hyaline or subhyaiine, on short denticles, I-celled, longcylindrical, may be somewhat curved; saprophytic. Similar to Calcarisporium but with dark conidiophore.
Description from Ichinoe (221).
Illustration: Selenosporella sp.; original, from fresh materials on decayed wood. (A) conidiophore; (B)
conidiogenous cell; (C) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
IDRIELLA
CONOPLEA
CALCARISPORIUM
SELENOSPORELLA
103
104
DESCRIPTIONS AND ILLUSTRAIIONS OF GFNERA
RHINOCLADIELLA Nannf. Conidiophores simple, or branched in some species, brown, upper sporebearing portion becomes elongated by sympodial growth; conidia (sympodulospores) apical on new
growing points, subhyaline to dark, mostly I-celled, ovoid to oblong-ellipsoid, dry; saprophytic;
frequently on wood.
Illustration: Rhinocladielta sp.; original, from fresh material on decayed wood. (A) habit of conidiophores; (B) conidiophores enlarged; (C) conidia. Reference (17).
PERICONIELLA Sacc. Conidiophores dark, upper portion branched, producing conidiogenous cells
and conidia apically and on new sympodial growing points; conidia (sympodulospores) 1-celled, dark,
ovoid or oblong.
Illustration: P. velutina; original, from herbarium material on Brajijum stellatifolium. (A) conidiophores;
(B) conidia. Reference (122).
VERTICICLADIUM Preuss. Conidiophores brown, single or in clusters, branched verticillately above;
conidia apical on new sympodial growing points; conidia (sympodulospores) 1-celled, hyaline or
subhyaline, not in slime droplets; differs from Verticicladiella in its dry spores.
Illustration: V. trijidium; redrawn from Hughes (187).
SYMPODIELLA Kendrick. Conidiophores solitary, simple, dark; conidia (sympodulospores) 1-celled,
hyaline, in unbranched chains, attached apically and laterally, cylindrical, with blunt ends; saprophytic, on
pine needles.
Illustration: S. acicola; redrawn from Kendrick (247).
OVULARIA Sacc. Conidiophores in clusters, mostly simple; conidia (sympodulospores) hyaline,
1-celled, ovoid or globose, apical on new sympodially formed growing points. See Hughes (210) for
synonymy with Ramularia Unger.
Illustration: O. avicularis. (A, B) conidiophores and conidia. Original, drawn from herbarium material
on Polygonum aviculare. Reference (386).
VERTICICLADIELLA Hughes. Conidiophores upright, tall, brown, branched only near apex,
penicillate; conidia (sympodulospores) hyaline, 1-celled, ovoid to clavate, often curved, apical on
sympodially formed new growing points, in slime droplets; parasitic or saprophytic. Compare with
Verticicladium and Leptographium. V. procera causes a root rot of white pine.
Illustration: V. peniciliaia; redrawn from Kendrick (250). (A) conidiophore with head of moist conidia;
(B) portion of conidiophore bearing conidia; (C) conidia. Redrawn by permission of the National
Research Council of Canada from the Canadial Journal of Botany, 40, pp. 771-779 (1962).
BELTRANIA Penzig. Setae brown, simple, pointed; conidiophores simple or less often forked, brown;
conidia (sympodulospores) biconic, 1-celled, brown with a paler middle band, borne single on denticles or
ovoid separating cells; saprophytic. Sec Pirozynski (331) for descriptions of related genera.
Illustration: B. indica; (A, C) conidiophores and conidia; (B) seta. Redrawn from Subramanian (395).
Other reference (191).
DESCRIPTIONS A N D ILLUSTRATIONS OF GENERA
„ 0
o Q0
„0c
JO
OVULARIA
BELTRANIA
105
106
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
BISPORA Corda. Mycelium dark; conidiophores dark, short, simple or sparingly branched; conidia
(blastophores) dark, oblong to ellipsoid, 2-celled or less often 3-celled, with thick, black septa; produced in
acropetalous chains; saprophytic on wood.
Illustration: B. punctata; original. (A, E) conidiophores and conidia; (B, C) conidiophores; (D) conidia.
(A-D) from fresh material on wood; (E) from culture.
AMPULLIFERINA Sutton. Superficial mycelium brown; hyphopodia lateral, brown, with a pore;
conidiophores short, simple, tapering at the base; conidia (arthrospores) 2-celled, brown, cylindrical,
truncate at both ends, catcnulate, formed by fragmentation; saprophytic on fallen leaves.
Illustration: A. persimplex; redrawn from Sutton (421). (A) mycelium with hyphopodia; (B) conidiophore
with chain of conidia; (C) conidia. Redrawn by permission of the National Council of Canada from the
Canadian Journal of Botany, 47, pp. 609-616 (1969).
CLADOSPORIUM Link. Conidiophores tall, dark, upright, branched variously near the apex, clustered
or single; conidia (blastophores) dark, 1- or 2-celled, variable in shape and size, ovoid to cylindrical and
irregular, some typically lemon-shaped; often in simple or branched acropetalous chains; parasitic on
t
higher plants or saprophytic.
V*i*
Illustration: (A) C.fulvum; original, from herbarium material on tomato leaf; (B) C. herbarum; original,
from fresh dead plant material. References (17, 90).
PSEUDOBOTRYTIS Krzem. and Badura. Conidiophores dark, erect, slender, simple, bearing at the
apex a number of slender divergent conidiogenous branches arising from the same level and bearing
conidia on somewhat enlarged denticulate tips; conidia (sympodulospores) dark, 1- or 2-celled, ovoid to
oblong; saprophytic.
Illustration: P. terrestris; (A) redrawn from Subramanian (403); (B, C) redrawn from Morris (299).
^ SPILOCAEA Fr. Mycelium subcuticular on the host, forming a stoma that bears upright conidiophores;
P$k$ conidiophores dark, 1-celled, short, simple, markedly annulate near the tip due to the new conidia being
pushed out through the apical conidial scars; conidia (annellospores) dark, typically 2-celled, although
t S/ >-? 1-cetled conidia may predominate, broadly ovoid to pyriform or angled and pointed, with a truncate base;
parasitic on higher plants; conidial states of Venturia. Compare with Fusicladium,
Illustration: S. pomi (Fusicladium dendriticum, Venturia inequalis); original. (A) section through
stroma; (B) conidiophores and conidia from fresh material on apple leaf. References (17, 205).
BALANIIJM Wallroth. Conidiophores solitary or in small groups septate, dark brown, thick, dichotomously branched, terminating in short conidiogenous cells; conidia (aleuriospores) 2-celled, thick-walled,
dark brown, smooth, dry, ovoid to pyriform, saprophytic, on decaying wood.
Illustration: B. stygium; redrawn from Hughes and Hennebert (214). Redrawn by permission of the
National Research Council of Canada from the Canadian Journal of Botany, 39, pp. 1505-1508 (1961).
DESCRIPTIONS AND ILLUSTRATIONS Ol GENERA
107
108
DESCRIPTIONS AND ILLUSTRATIONS Of GENERA
CLADOBOTRYUM Corda. Conidiophores erect, hyaline, often arising from aerial mycelium, branching
irregularly or verticillately and repeatedly, terminating in groups of phialides that taper toward the apex;
conidia (phialospores) hyaline, mostly 2-ceIled (sometimes more), ovoid to oblong, held together in
irregular or tangled chains; imperfect state of Hypomyces; saprophytic or parasitic on fleshy fungi.
Illustration: Cladobotryum sp.; original from culture. (A) conidiophore; (B) sporogenous cells;
(C) conidia. References (17, 58).
CYLINDROCLADIUM Morgan. Conidiophores upright, hyaline, regularly and repeatedly dichotomously or trichotomously branched, each terminating in two or three phialides; typically with a slender
elongated sterile branch terminating in a globose or ellipsoid swelling; conidia (phialospores) hyaline, 2- or
several-celled, cylindrical, borne singly but held together in bundles by mucilage; parasitic on roots or
saprophytic; small, yellow-brown sclerotia produced.
Illustration: C. scoparium; original, from culture. (A) conidiophores; (B) conidiophore with elongated
branch and terminal vesicle; (C) conidia. References (37, 39, 302).
DIPLOSPORIL'M I.ink. Conidiophores erect, well developed, septate, irregularly branched, ultimate
branches (phialides) tapering upward, hyaline; conidia (phialospores) produced successively at the apex
and held together in loose clusters, not catenulate, 2-celled, hyaline; saprophytic.
Illustration: D. flavum; redrawn from Tubaki (450). (A) conidiophores; (B) phialides; (C) conidia.
HELISCUS Sacc. Submerged, aquatic, with branched, septate mycelium; conidiophores simple or
sparingly branched, bearing one or more phialides; submerged conidia (phialospores) hyaline, 2-celled,
broader at the apex, usually bearing 3 short, apical protuberances; saprophytic, aquatic.
Illustration: H. aquaticus; redrawn from Ranzoni (346).
RHYNCHOSPORIUM Heinscn. Mycelium subcuticular at first, later developing into a superficial, loose
stroma; conidiophores reduced to cells of stroma; conidia (blastospores) hyaline. 2-celled, frequently
unequal, and often with a short lateral beak on the apical cell; parasitic, producing leaf spots, chiefly
on grasses.
Illustration: R. secalis; original, from leaf spot on rye. (A) hyphae from stroma showing conidiogenous
cells; (B) conidia. Reference (49).
TRICHOTHECIlfM Link. Conidiophores long, slender, simple, septate, bearing conidia apically. singly,
or successively by slight growth of conidiophore apex, held together in groups or chains, not end to end;
conidia (meristem arthrospores — may appear to form as blastospores) hyaline or brightly colored,
2-celled, ovoid or ellipsoid; saprophytic or weakly parasitic.
Illustration: T. roseum; original, from culture. (A-D) successive development of conidia. References
(227, 254).
DESCRIPTIONS AND ILLUSTRATIONS Of GENERA
CLADOBOTRYUM
CYIINDROCLADIUM
HEUSCUS
DIPLOSPORIUM
0 <x§p
d?
c
RHYNCHOSPORIUM
TRICHOTHECIUM
1 09
110
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
ARTHROBOTRYS Corda. Conidiophores long, slender, simple, septate, hyaline, slightly enlarged at the
apex and spore-bearing regions. New growing points formed sympodially or irregularly, conidia
(sympodulospores) hyaline, unequally 2-ceIled, ovate-oblong, borne on peglike denticles in loose dry
clusters; saprophytic or parasitic on nematodes. Compare with Candelabrella,
Illustration: A. oligospore; original, from culture. (A) conidiophores bearing conidia and showing
prominent denticles; (B) conidia. References (61,106, 159).
CANDELABRELLA Rifai and Cooke. Mycelium hyaline; conidiophores slender, erect, straight,
hyaline, tall, terminated by a small candelabrumlike branching system of the conidiophore apex; conidia
(sympodulospores) apical and on new sympodial or irregular branches, hyaline, unequally 2-celled,
obpyriform to ellipsoid; saprophytic or destroying nematodes. Species formerly placed in Arthroboirys.
Illustration: C. musiformis (Arthrobotrys musiformis); original, from culture. (A) conidiophores bearing
conidia on elongated denticles; (B) conidia. Reference (355).
'^x\ DACTYLARIA Sacc. Conidiophores more or less erect, simple, short, sometimes little differentiated
^ L ,i\ fr°m t n e mycelium, hyaline, septate, denticulate and sometimes enlarged at the apex; conidia (sympodulo( spores) hyaline, 2- to several-celled, cylindrical or clavate, sometimes longer and single at apex;
\ saprophytic or parasitic on nematodes. See Bhatt and Kendrick (31) for synonymy of Diphrhinotrichum.
Illustration: Dactylaria sp.; original, from fresh material on decaying wood. (A) conidiophores; (B)
conidia. References (61, [04).
DIDYMARIA Corda. Conidiophores arising from leaf surface in loose groups, simple; conidia
(sympodulospores) hyaline, 2-celled, oblong, borne singly; parasitic on leaves.
Illustration: D, conferta; original, from herbarium material. (A) conidiophores on surface of leaf;
(B) group of conidiophores; (C) conidia.
RAMULARIA Sacc. Conidiophores growing out through stomata of host leaves, clustered, short,
hyaline or subhyaline, frequently curved or bent, with prominent conidial scars; conidia (sympodulospores) hyaline, cylindrical, typically 2-celled, but many 1-celled and a few 3-celled, frequently in short
chains; parasitic on plants, causing leaf spots,
Illustration: R. lulasnea (Mkosphaereliafragahae); original, from herbarium material on strawberry leaf.
(A) habit on leaflet; (B) conidiophores; (C) conidia.
GENICULARIA Rifai and Cooke. Conidiophores erect or ascending, hyaline, branching sympodially;
conidia (sympodulospores) hyaline, unequally 2-celled, with large rounded apical cell, obovoid, formed
singly on new extended sympodial branches from below previous conidium; trapping and destroying
nematodes or saprophytic.
Illustration: G. cystospora; redrawn from Rifai and Cooke (355).
DESCRIPTIONS AND ILLUSTRAFIONS OF GENERA
ARTHROBOTRYS
CANDELABRELLA
B
C
DIDYMARIA
RAMULARIA
GENICULARIA
111
11 2
DESCRIPTIONS AND IUUSTRATIONS OF GENERA
PASSALORA Fr. Mycelium internal; conidiophorcs emerging in tufts from stroma, simple or sparingly
branched, dark; conidia (sympodulospores) subhyalinc to dark, 2-celled, formed terminally and at apex of
sympodial new growing tips; parasitic.
Illustration: P. bacilligera. (A) cluster of conidiophores arising from stroma; (C) conidiophores;
(CJ conidia; redrawn from Hughes (205). Reference (78).
ASPERISPORIL'M Maubl. Stroma subepidermal in the host, bursting through the epidermis, bearing
short, crowded conidiophores; conidia (sympodulospores) dark, rough, 2-celled, produced at apex of
sympodially formed new growing tips of conidiophorcs; parasitic.
Illustration: A. caricae. (A) section through stroma and cluster of conidiophores; (B) conidia; redrawn
from Hughes (205).
SCOLECOTRICHUM Kunzeex Fr. Conidiophores in loose clusters, pigmented, simple, bearing conidia
terminally on sympodial new growing points; conidia (sympodulospores) dark, 2-celled, ovoid or oblong,
often pointed; parasitic. Similar to and may belong to Cercosporidium.
Illustration: S. graminis: original, from herbarium material on leaves of Dactylis. (A) habit of
conidiophores on leaf; (B, C) clusters of conidiophores; (D) conidia.
FUSICLADIUM Bon. Mycelium as in Spihcaea; conidiophores dark, short, denticulate with conidial
scars, young conidia produced successively at apex of sympodial new growing lips; conidia (sympodulospores) dark, ellipsoid to obpyriform, typically 2-celled, although l-cclled may predominate; parasitic on
higher plants. Compare with Spihcaea. Some species are conidial states of Venturia.
Illustration: F. pirina (conidial state of Venturia pirina); original, from herbarium material on pear
leaf. (A) conidiophores bearing conidia; (B) conidia. References (78, 205).
POLYTHRINCIUM Kunze and Schum. Conidiophores in dense clusters on host leaves, dark, simple,
with enlarged basal cell, regularly bent, giving a wavy appearance caused by successive sympodial growth
at apex; conidial scars prominent, on same side of conidiophore; conidia (sympodulospores) dark,
unequally 2-celled, the apical cell broader and rounded, easily deciduous; parasitic on leaves.
Illustration: P. trijolii (conidial state of Cymadothea thfolia); original, from fresh material on white clover
leaf. (A) cluster of conidiophores; (B) wavy conidiophores and conidia; (C) conidia. References
(17,199, 475).
CORDANA Preuss. Mycelium dark; conidiophores dark, upright, slender, simple, bearing a small,
compact head of conidia; conidia (sympodulospores) dark, 2-celled, ovoid to broadly ellipsoid;
saprophytic.
Illustration: C pauciseptata; original, from culture. (A) conidiophore with cluster of conidia;
(B) conidiophores; (C) conidia; (D) enlarged apex of conidiophore showing conidial attachment.
References (17, 209).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
POLYTHRINCIUM
CORDANA
113
114
DFSCRIPTIONS AND ILLUSTRATIONS OF GENERA
SCOIXCOBASID1UM Abbott. Conidiophores (or conidiogenous cells) arising from aerial hyphae or
ropes of hyphae, single or in groups, relatively short, sometimes 1-cellcd, irregular in shape; conidia
(sympodulospores) olive-brown, I-celled or frequently 2- to 4-celled, ovoid, cylindrical or Y-shaped,
produced on prominent denticles at apex of conidiogenous cells; saprophytic.
Illustration: Scolecobasidium sp.; original, from fresh material on decayed wood. (A) mycelium and
conidiophores; (B) conidiophores with prominent denticles; (C) conidia. References (14, 17).
DIPLOCOCCIUM Grove. Mycelium partly superficial; conidiophores erect or ascending, frequently
branched, brown; conidia (porospores) mostly 2-celled, short, brown, usually formed in acropetalous
chains, developing through minute pores in wall or upper portion of conidiophores; differs from
Spadkoides in branched conidiophores and catenulate conidia; saprophytic on wood or bark.
Illustration: D. spicatum; redrawn from Ellis (119). (A) branched conidiophore; (B) conidiophores
bearing catenulate conidia; (C) conidium.
SPADICOIDES Hughes. Conidiophores mostly simple, erect, determinate, brown; conidia (porospores)
develop singly through pores in apical or lateral wall or conidiophore, dark, ovoid to ellipsoid I- to
4-celled in different species; saprophytic on decayed wood. Differs from Diplococcium in the simple
conidiophores and conidia not in chains.
Illustration: (F-F) S. ohovata; (A-D) S. bina; original, from fresh material on decayed wood.
(A) conidiophores with attached conidia; (B) portion of simple conidiophore; (C) enlarged apex of
conidiophore showing conidial attachment; (D) conidia. Reference (119).
MtJROGENEl-LA Goos and Morris. Conidiophores variable in length or absent; conidia (alcuriospores)
single, terminal, dark, several-celled, ovoid to elliptical; conidia are murogenous (originating as
expansions of the entire conidiophore tip); saprophytic in soil.
Illustration: M. terricola; redrawn from Goos and Morris (153). (A) sessile conidia and conidia produced
on short conidiophores; (B) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
MUROGENELLA
115
1 16
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
CEPHALIOPHORA Thaxt. Conidiophore short, with enlarged, rounded apical cell, bearing simultaneously a dense cluster of conidia on all sides; conidia (botryoblastospores) lightly pigmented, usually 4or more-celled, obovoid to elongate, narrower at the base; saprophytic on dung or decaying plant
materials.
Illustration: C. tropica; redrawn from Thaxter (440). Reference (477).
PSEUDOTORULA Subram. Conidiophores dark, simple, torulose, with apical rounded conidiogenous
cell; conidia of two types, brown, 4-celled (blastospores) in acropetalous chains, and long, slender,
several-celled scolecospores.
Illustration: P. heterospora; redrawn from Subramanian (407). (A) conidiophore and phragmospores;
(B) both types of conidia; (C) scolecospore.
DWAYABEEJA Subram. Much like Pseudoforula but differing in that conidia (blastospores) are not
in chains.
Illustration: D. sundara; redrawn from Subramanian (407). (A) conidiophore; (B) phragmospores;
(C) scolecospores.
MICROSPORUM Gruby. Conidiophores slender, simple, determinate, bearing apically a single, large
macroconidium; macroconidia (aleuriospores) fusoid. several-eel led, hyaline; microconidia also formed
on sides of hyphae; causing dermatomycoses of animals and man.
Illustration: M. gypseum; original, from culture. (A) conidiophores and conidia; (B) development and
separation of conidium. References (59, 129).
TRICHOPHYTON Malmsten. Microconidia hyaline, small, l-celled, on sides of hyphae; macroconidia
(aleuriospores) large, several-celled, thin-walled, hyaline, clavate with rounded apex; causing dermatomycoses in man.
Illustration: T. violaceum. (A) microconidia; (B) macroconidia; redrawn from Georg (143). References
(129,142, 143, 144).
FUSOMA Corda. Conidiophores short, simple, determinate; conidia (aleuriospores) hyaline, severalcelled, fusoid to cylindrical; parasitic on higher plants.
Illustration: F. rubricosa; original, from herbarium material of leaves of Catamagrostis scabra.
(A, B) conidiophores and conidia.
CAMPOSPORIUM Harkn. Conidiophores straight or bent, brown; conidia (aleuriospores) apical,
single, cylindrical with rounded ends, pale brown, several-celled, apical cell frequently with I to 3 hyaline,
filiform appendages.
Illustration: C. antennatum; redrawn from Tubaki (450). (A-C) conidiophores and conidia. References
(450, 194, 347).
SEPTONEMA Corda. Conidiophores dark, branched; conidia (blastospores) subhyaline to dark brown,
typically 3- to several-celled; cylindrical to fusoid, catenulate in acropetal simple chains; saprophytic or
parasitic.
Illustration: S. secedens; redrawn from Hughes (196). (A, B) conidiophores with catenulate conidia.
References {175, 202).
DESCRIPTIONS AND II LUSTRATIONS OF GLNERA
M
DWAYABEEJA
CEPHALIOPHORA
PSEUDOTORULA
FUSOMA
CAMPOSPORIUM
117
118
DESCRIPTIONS AND ILLUSTRATIONS OF GENFRA
CERATOPHORUM Sacc. Conidiophores dark, short, simple, determinate; conidia (aleuriospores or
blastosporcs) dark, 3- to several-celled, single, fusoid to cylindrical, apical cell hyaline, often curved or
hooked; saprophytic.
Illustration: C. uncinalum; original, drawn from herbarium material on Hicora leaves. (A, B) conidiophores and conidia. References (17, 184).
CLASTEROSPORIUM Schw. Mycelium superficial, bearing hyphopodia; conidiophores dark, short,
determinate; conidia (aleuriospores) dark, 3- to several-celled, ovoid to long cylindrical, somewhat
narrower at the ends; parasitic on higher plants.
Illustration: C. caricinum; original, from herbarium material on leave of Carex. (A, B) conidiophores,
hyphopodia and conidia. References (113, 114).
MONACROSPORIUM Subr. Conidiophores tall, usually simple, hyaline, slender, determinate; conidia
(aleuriospores) single, apical, hyaline, several-celled, usually fusoid with one cell (near middle) larger;
compare with Dacty/ella; saprophytic in soil or wood or parasitic on nematodes.
Illustration: Monacrosporium sp.; original, from culture. (A) conidiophore and conidium; (B-D) stages
of development of a conidium; (E) conidium. Reference (60).
PHRACiMOCEPHALA Mason and Hughes. Conidiophores pigmented, simple, single, fascicled or in
synnemata; conidia (aleuriospores) dark, more than 3-celled, ovoid to pyriform, cells unequally colored;
saprophytic on dead plant material. Compare with Endophragmia.
Illustration: P. cookei; redrawn from Mason and Hughes (283). (A) clustered conidiophores with
attached conidia; (B) conidia.
ENDOPHRAGMIA Duvernoy and Maire. Conidiophores simple, brown, mostly single, often
proliferating pcrcurrently; conidia (aleuriospores) 2- to several-celled, brown to black, single, apical;
saprophytic.
Illustration: E. mirabilis; original, from decayed wood. (A) conidiophore bearing apical conidia; (B) apex
of conidiophores showing annellations; (C) conidia; (D) E. taxi. References (4, 114, 117).
ANNEEEOPHORA Hughes. Conidiophores brown, simple, slender, elongating by successive proliferations through the conidial scars; conidia (anncllospores) brown, mostly 3- to several-celled, obclavate to
fusoid; mycelium superficial on leaves.
Illustration: A. solani; redrawn from Hughes (192). (A) conidiophores showing annellations; (B) conidia.
Reference (117).
DEIGHTONIEEEA Hughes. Conidiophores arising from within epidermal cells, short, upper portion
distinctly annellated; conidia (anncllospores) dark, 3-celled; parasitic.
Illustration: D. anmdinacea. (A) conidiophores arsing from epidermis of host; (B) conidia; redrawn from
Hughes (205). Reference (17).
TRICHOCEADIUM Har/. Conidiophores short or absent; conidia (aleuriospores) dark, mostly 2- to
several-celled, ovoid to ellipsoid to clavate; saprophytic on wood.
Illustration: T. catuulense; original. (A) sessile conidia; (B) conidiophores and conidia. References
(158,200,211).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
TRICHOCLADIUM
ANNELLOPHORA
119
120
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
DENDRYPHIOPSIS Hughes. Conidiophores dark, stout, upright, dendritically branched, ultimate
branches producing solitary apical conidia; conidia (porospores or blastospores) dark, 4- to several-celled,
cylindrical, straight or slightly curved; saprophytic on wood.
Illustration: D. atra; original. (A, B) from fresh material on decayed wood; (C) from pure culture isolated
from decayed wood. Reference (206).
STIGMINA Sacc. Conidiophores dark, rather short, simple, straight or bent, often arising in clusters
from stromalike tissue and protruding through stomata of leaves, producing conidia apically and
proliferating through previous spore scars, leaving annellate scars; conidia (annellospores) dark, 3- to
several-celled, ovoid to ellipsoid; parasitic or saprophytic.
Illustration: 5 " . plantani; original, from h e r b a r i u m material on leaves of Phntanus occidentalis.
(A) section of leaf through clusters of conidiophores; (B) conidiophores with developing conidia;
(C) conidia. References (118, 199, 304).
DICHOTOMOPHTHORA Mehrlick and Fitzpatrick. Conidiophores brown, branching, dichotomous to
subdichotomous, elongated, terminally branched, 4- to 8-lobed, each lobe bearing a single conidium;
conidia (porospores or blastospores) dark, ovoid to elongate-ovoid, 1- to 6-celled; parasitic on Portulaca.
Illustration: / ) . portulacae; redrawn from Mehrlich and Fitzpatrick (285). (A) conidiophore; (B)
enlarged portion of conidiophore and conidia; (C) conidia.
SPONDYLOCLADIELLA Linder. Conidiophores dark, single or in small groups, branched; conidiogenous cells short, stubby, single or in groups; conidia (porospores or blastospores) dark, mostly 3-celled,
oblong, borne singly, formed through small pores in apex of condiogenous cells; saprophytic, often on
hymenomycetes.
Illustration: S. botrytioides; redrawn from Linder (265). (A) conidiophores showing short, stubby
sporogenous cells; (B) conidia.
CORYNESPORA Gussow. Mycelium internal in leaf; conidiophores emerge through leaf epidermis,
slightly or conspicuously swollen at apex, simple, single, determinate or in tufts, proliferating terminally
through scar of previous conidium; conidia (porospores) terminal, single or sometimes in short chains,
brown, several-celled (pseudoseptate), with a thick, colorless exospore and prominent, dark basal scar;
parasitic on leaves. Compare with Helminthosporium.
Illustration: C. cassiicoia; redrawn from Luttrell (273). (A) conidiophores and conidia; (B) conidium.
References (119, 468).
SPORIDESMIUM Link. Conidiophores simple, determinate, brown; conidia (aleuriospores) severalcelled, apical, single, brown, obclavate to long, fusoid; saprophytic or parasitic. S. sderotivorum is
parasitic on sclerotia and has a secondary Selenosporella conidial state.
Illustration: (A) S. tropicale; (B) S. folliculatum; redrawn from Luttrell (273); (C) S. sderotivorum,
original from culture; (D) Selenosporella state. References (118, 119, 455).
DESCRIPTIONS AND ILLUSTRATIONS Oh GLNERA
DICHOTOMOPHTHORA
121
SPONDYLOCLAD1ELLA
122
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
,
.CLIRVULARIA Boedijn. Conidiophores brown, mostly simple, bearing conidia apically or on new
i>Vsympodial growing points; conidia (porospores) dark, end cells lighter, 3- to 5-celled, more or less
T .-fusiform, typically bent, with one of the central cells enlarged; parasitic or saprophytic.
Illustration: C. lunata; original, from culture. (A-C) conidiophores and conidia; (D) conidia. References
(121, 308, 309, 322, 398).
HETEROSPORIUM Klotzch. Conidiophores dark, simple, conidia (blastospores, sympodulospores)
typically 3- to several-celled, cylindrical, wall often echinulate or verrucose, single or in acropetal chains;
causing leaf spots or saprophytic. Compare with Caldosporium.
Illustration: H. gracile; original, from herbarium material on Iris leaf. (A) clusters of conidiophores;
(B) conidia. Reference (238).
CERCOSPORIDIUM Erie. Stroma present; conidiophores densely fasciculate, brown, usually simple;
conidia (sympodulospores) single and apical on new sympodial growing points, clavate, cylindrical to
obclavate, mostly pale brown, few- to several-celled; conidial scars conspicuous; on living leaves, causing
leaf spots. Compare with Fusicladium, Passalora and Cercospora.
Illustration: C. personatum; redrawn from Deighton (78). (A) section through stroma; (B) apex of
conidiophores; (C) conidia.
DRECHSLERA Ito. Conidiophores brown, mostly simple, producing conidia singly at apex through
small pores, continuing growth sympodially from a point below apex and then forming a second spore on
new apex; conidia (porospores) dark, several-celled (phragmosporous), cylindrical, germinating from any
or all cells; parasitic or saprophytic. Compare with Bipolaris. Formerly included under Helminthosporium.
Illustration: (A-C) D. avenaciwn; redrawn from Luttrell (272). (A) conidiophores and conidia on leaf;
(B) conidiophore showing scars; (C) germinating conidium; (D) D. maydis, conidia; (E) D. carbonum,
conidia. References (96, 273, 372, 373).
GONATOPHRAGMIUM Deighton. Conidiophores well developed, brown, bearing conidia on short
pegs on swellings or nodules; conidia (sympodulospores) mostly 2- to 4-celled, pale brown, cylindricalclavate; parasitic on leaves.
Illustration: G. mori; redrawn from Cejp and Deighton (52). (A) conidiophores; (B) conidia.
DESCRIPIIONS AND ILLUSTRATIONS OF GENERA
GONATOPHRAGMIU M
DRECHSLERA
123
124
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
HELMINTHOSPORIUM Link ex Fr. Mycelium dark, often in stubstrate; stromata often present;
conidiophores single or clustered, tall, erect, brown, simple; conidia (porospores) develop laterally through
pores beneath septa while apex of conidiophore is still growing, often appearing in whorls, single,
subhyaline to brown, obclavate, phragmosporous, pseudoseptate, with prominent basal scar; parasitic or
saprophytic. Shoemaker (372-373) restricts the genus Helminthospohum to lignicolous species and
classifies grarainicolous species in Bipolaris and Drechslera,
Illustration: H. velutinum (Spondylocladium atrovirons); redrawn from Luttrell (273). (A) conidiophores
and conidia arising from stroma; (B) enlarged apex of conidiophore showing pores; (C) conidiophores
and conidia from culture; (D) H. solani, original from culture. References (96, 272, 273, 372, 373, 375).
CACUMISPORIUM Preuss. Conidiophores dark, upright, septate, simple, bearing an apical head of
conidia; conidia (sympodulospores or phialospores) dark, at first hyaline, mostly 4-celled, oblong to
fusoid, straight or curved, produced on successively new growing points on hyaline projection of the
conidiophore and aggregating in moist head; saprophytic. Conidiophorc apex has been interpreted by
some as a phialide.
Illustration: Cacumisporium sp.; original, from decayed wood. (A) conidiophore and conidia;
(B) conidial attachment at apex of conidiophore; (C) enlarged apex of conidiophore with conidia;
(D) conidia. References (151, 206).
DENDRYPHION Wall. Conidiophores erect, dark, branched variously on upper portion, spore scars
prominent; conidia (porospores) several-celled (phragmosporous), dark, catenulate, produced apically
through pores in the conidiophores and new sympodial growing points; saprophytic on wood. See Barron
(17) and Reisinger (353) for opinions on the genus Dendryphiella.
Illustration: Dendryphion sp.; original, from culture obtained from decayed wood. (A) conidia and
conidiophores; (B) conidiophores; (C) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
HELMINTHOSPORIUM
CACUMISPORIUM
DENDRYPHION
125
1 26
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
BIPOLARIS Schoemaker. Conidiophores brown, mostly simple, producing conidia through apical pore,
resuming growth sympodially and forming conidia on successive new tips; conidia (porospores) brown,
several-celled (phragmosporous), elliptical, straight or curved, germinating by one germ tube at each end;
parasitic, chiefly on grasses; perfect stage, where known, Cochliobolus. Formerly included under
Helminthosporium. Ellis (124) places this genus in Drechslera.
Illustration: B. sorokinianum (B. sativum); (A-C) redrawn from Luttrell (272). (A) conidiophore and
conidia on leaf; (B) conidiophore showing scars; (C) germinating conidium; (D) original, from pure
culture. References (96, 273, 372).
PLEUROPHRAGMIUM Constantin. Stroma sometimes present; conidiophores single or in groups,
brown, pale near apex, septate, new growth sympodial; conidia (sympodulospores) pale brown, mostly
3-to 5-celled, phragmosporous, broadly ellipsoid to subclavate with rounded apex; conidial scars, mostly
lateral, flat or on raised circles (described by Ellis as borne on denticles); saprophytic on wood or
herbaceous stems. Compare with Spiropes.
Illustration: Pleurophragmium sp.; original, fresh material on decayed wood. (A) habit of conidiophores;
(B) simple conidiophore; (C) enlarged apex of conidiophores showing numerous scars; (D) conidia.
Reference (123).
PLEUROTHECIUM Hohnel. Conidiophores single or in loose clusters, simple, dark, narrower and
paler at apex; new growing points produced sympodially and producing new conidia; fertile area recurved
to produce a curved cyme; conidia (sympodulospores) in moist heads, hyaline, typically 4-celled, ellipsoid
or slightly curved.
Illustration: P. recurvaium; original, from fresh material on decayed wood. (A) habit of conidiophores
showing slime heads; (B) conidiophores and conidia; (C) cluster of conidia on conidiophore. Reference
(17, 152).
BRACHYSPORIUM Sacc. Conidiophores brown, pale at apex, erect, solitary or in small clusters,
simple, septate; conidia (sympodulospores) dark, ovoid to obovoid, unequally 3- to 4-celled, basal cell and
apical cell may be nonpigmented, attached to apical cell of conidiophore by a slender pedicel, part of
which remains attached to the fallen conidium; saprophytic on wood and bark.
Illustration: (A, B) B. nigrum; (C, D) B. obovatum; all original, from fresh material on decaying wood.
References (17, 121, 194).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
m
PLEUROPHRAGMIUM
PLEUROTHECIUM
C
£3
BRACHYSPORIUM
D
127
128 DESCRIPTIONS A N D I L L U S T R A T I O N S OF GFNERA
NAKATAEA Hara. (VAKRABEEJA Subram.) Conidiophores simple, single, cylindrical, new growth
sympodial, with prominent denticulate conidial scars near apex; conidia (sympodulospores) 3- to fewcelled, phragmosporous, fusoid, straight to curved, light brown; parasitic on plants.
Illustration: V. sigmoidea; redrawn from Luttrell (272). (A) conidiophores and conidia; (B) apex of
conidiophore.
DACTYLELLA Grove. Conidiophores tall, slender, simple, hyaline; conidia (sympodulospores,
aleuriospores) hyaline, several-celled, ellipsoid, fusoid to cylindrical, borne singly at apex or in a loose
cluster on prominent denticles; saprophytic or parasitic on nematodes.
Illustration: (A-C) D. brochopaga; original, from culture. (A-C) conidiophores and conidia;
(D) conidiophore and conidium of D. lepiospora; original, from material on decaying wood. References
(60, 61).
PYRICULARIA Sacc. Conidiophores long, slender, mostly simple; conidia (sympodulospores)
obpyriform to nearly ellipsoid, attached at the broader end; hyaline, 2- to 3-celled, parasitic, chiefly
on grasses.
Illustration: P. grisea; original, from leaf of Setaria.
PLEIOCHAETA Hughes. Conidiophores simple; conidia (sympodulospores) dark, mostly 5-celled,
cylindrical to ellipsoid, sometimes slightly curved, the middle cell thick-walled and darker, bearing 1 to 4
long, slender, apical, hyaline appendages; parasitic, on plants.
Illustration: P. setosa; redrawn from DuPleissis and Truter (107). (A, B) conidiophores and appendaged
conidia.
SEPTOCYLINDRIUM Bon. Conidiophores hyaline, simple; conidia (sympodulospores) hyaline, 2- to
several-celled; oblong to cylindrical, catenulate; parasitic on higher plants or saprophytic. Compare with
Ramularia.
Illustration: S. aromaticum; original, from herbarium material on leaves of Acorum calamus.
(A, B) conidiophores and conidia.
CERCOSPORELLA Sac. Conidiophores hyaline, slender; conidia (sympodulospores) hyaline, severalcelled, oblong, cylindrical to filiform, straight or curved; parasitic on higher plants; compare with
Cercospora.
Illustration: C persica; original, from herbarium material on peach leaf. (A) conidiophores and conidia;
(B) conidia. Reference (81).
.SPERMOSPORA Sprague. Conidiophores hyaline or nearly so, short, grouped; conidia (sympodulof^jspores) hyaline, with distal cell elongated, attenuated, mostly 3- to 4-celled; parasitic on grasses, causing
" leaf spots. Compare with Cercospora.
Illustration: A. avenae; original, from culture. (A) conidiophores and conidia; (B) conidia. References
(79, 385, 386).
CERCOSPORA Frej^Xonidiophores dark, simple, arising in clusters and bursting out of leaf tissue,
, bearing conidia successively on new growing tips; conidia (sympodulospores) hyaline or gray, long
(^^cylindrical to filiform, several-celled; parasitic on higher plants, commonly causing leaf spots.
Illustration: C. apii; original, from prepared slide of section through leaf. (A) cluster of conidiophores;
(B) conidia; (C) C. zea-niaydis conidia. References (55, 81, 82, 83, 84).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
W§4
PYR1CULARIA
DACTUEUA
NAKATAEA
fl
SEPTOCYLINDRIUM
CERCOSPORELLA
PIEIOCHAETA
I
V
CERCOSPORA
SPERMOSPORA
129
130
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
-
\
.,
\
FUSARIUM Link. Mycelium extensive and cotton-like in culture, often with some tinge of pink, purple,
or yellow in the mycelium on medium; conidiophores variable, slender, and simple, or stout, short,
branched irregularly or bearing a whorl of phialides, single or grouped into sporodochia; conidia
(phialospores) hyaline, variable, principally of two kinds, often held in small moist heads; macroconidia
several-celled, slightly curved or bent at the pointed ends, typically canoe-shaped; microconidia I-celled,
ovoid or oblong, borne singly or in chains; some conidia intermediate, 2- or 3-celled, oblong or slightly
curved; parasitic on higher plants or saprophytic on decaying plant material. A large and variable genus,
sometimes placed in the Tuberculariaceac because some species produce sporodochia. Thick-walled
chlamydospores common in some species.
Illustration: Fusarium spp.; original, from culture. (A) hyphae with simple conidiophores; (B) variable
conidiophores; (C) a loose sporodochium formed by branched conidiophores; (D) conidia. References
(370, 444).
DACTYLIUM Nees. Conidiophores slender, branched verticillately; conidia (phialospores or sympoduiospores) borne singly or in small clusters on slightly elongating branches, hyaline 3- to 4-celled; saprophytic
or parasitic on fleshy fungi; conidial states of Hypomyces. See Barron (17) for a discussion of Dactylium.
Compare with Cladobotryum.
Illustration: D. dendroides; original from culture. (A, B) conidiophores and conidia; (C) conidia
enlarged. Reference (258).
CYL1NDROCARPON Wollen. Conidiophores erect, slender, hyaline, simple or branched irregularly,
''terminating in slender phialides, phialides usually with conspicuous collarette; conidia (phialospores)
mostly 3- to 4-celled but often variable, hyaline, cylindrical, produced successively and aggregating in
.j-small fascicles; saprophytic or parasitic. Imperfect states of Necfria. Resembling Fusarium but larger,
conidia typically not curved.
Illustration: Cylindrocarpon sp.; original, from culture. (A) conidiophores with attached conidia; (B)
conidia. Reference (38).
FUSARIELLA Sacc. Conidiophores pigmented, typically branched, bearing conidia terminally on
slender phialides; conidia (phialospores) dark, 3- to 4-celled, cylindrical, curved, borne in basipetal chains,
not end to end, each conidium attached at the side of the conidium below; saprophytic on plant material.
Illustration: F. obstipa; drawn from photographs by Pollack (336). (A) conidiophore and developing
conidia; (B) chain of conidia. Reference (182).
SPOROSCHISMA Berk, and Dr. Conidiophores dark, upright, stout, simple, bearing conidia
endogenously; conidia (phialospores) dark, 3- to 4-celled, cylindrical, sometimes in chains; saprophytic on
decaying vegetation.
Illustration: S. mirabile; original, from culture. Mycelium, conidiophores, and endoconidia. References
((25, 173, 183).
DESCRtPTlONS AND ILLUSTRATIONS OF GtNERA
131
[1 - G % <J *>
FUSARIUM
<CED
c
CYLINDROCARPON
<HD
DACTYLIUM
SPOROSCHISMA
FUSARIEUA
1 32
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
ALTERNARIA Nees. Conidiophores dark, mostly simple; determinate or sympodial, rather short or
elongate; conidia (porospores) dark, typically with both cross and longitudinal septa; variously shaped,
obclavate to elliptical or ovoid, frequently borne acropetally in apical simple or branched appendage;
parasitic or saprophytic on plant material.
Illustration: (A-D) Alternaria sp.; (E) A. solani; both original, from culture. (A) conidiophore and chain
of conidia; (B) simple conidiophore showing apical pore; (C) proliferating conidium; (D) conidia.
References (239, 306, 376).
STEMPHYL1UM Wallr. Conidiophores dark, mostly simple with darker terminal swelling, short to
" long, bearing a single, terminal conidium, or successive conidia on new growing tips, conidiophore often
/(? proliferating through ofd conidial scar; conidia (porospofes) dark, with cross and longitudinal septa,
variable in shape, frequently globose, broadly ellipsoid, or ovoid, often constricted at major septum;
parasitic or saprophytic.
*
Illustration: 5 " . sarcinaeforme; original, from culture. (A) conidiophores and conidia; (B) c o n i d i o p h o r e ;
(C) conidiophore proliferating through conidial scar. References (376, 377).
ULOCLADIUM Preuss. Conidiophores indeterminate, sympodial, dark, mostly simple, septate; conidia
(porospores) dark, dictyosporous, usually without constriction at major septum, borne singly, apical, and
on new sympodial growing points; saprophytic. Compare with Alternaria and Stemphylium.
Illustration: IJlocladiwn sp.; original, from culture. (A) conidiophores showing development of conidia;
(B) conidiophore showing conidial scars; (C) conidia. Reference (376).
PITHOMYCES Berkeley and Broome. Conidiophores short, simple, peglike, arising laterally from
mycelium, subhyalinc; conidia (aleuriospores) single, apical, mostly several-celled (dictyosporous), mostly
broadly elliptical, oblong to pyriform or irregular, commonly vcrrucose or echinulate, usually detached by
fracture of wall of conidiophore; saprophytic.
Illustration: P. chartarum; original, from culture. (A) mycelium, short conidiophores, and conidia; (B)
conidia. Reference (17).
ACROSPEIRA Berk, and Br. Conidiophores short, simple, dark, variable, conidia (aleuriospores) apical,
single, mostly 3- or 4-celled, cells arranged irregularly, apical cell enlarged, darker; hyaline phialides
present, borne singly and producing chains of small, ovoid, hyaline conidia (phialospores).
Illustration: A. mirabilis; redrawn from Wiltshire (473). (A) dark dictyospores; (B) phialides and chains
of small conidia.
DESCRIPTIONS-A'ND ILLUSTRATIONS OF GENERA
STEMPHYUUM
ALTERNARIA
PITHOMYCES
ULOCLADIUM
ACR05PEIRA
1 33
J 34 DESCRIPTIONS AND MUSI RATIONS Oh GENERA
DICTY0ARTHR1NRIM Hughes. Conidiophores much like Arthrinium (meristematic at base), simple,
crowded, straight or curved, subhyaline, with thick, dark septa; conidia (mcristem blastospores) 4-celled;
cross-shaped, dark brown, apical and lateral on conidiophore; saprophytic.
Illustration: D. quadralum; redrawn from Subramanian (396). (A) conidiophore and conidia; (B)
conidia. Reference (198).
CONIOSPORIl'M Link. (= SIRODESM1UM deNot) Conidiophores dark, densely clustered, arising
from a stroma, bearing terminal chains of conidia; conidia (meristem arthrospores) dark, elongate,
septate, sometimes with longitudinal walls, borne in single chains, developing basipetally; saprophytic
on wood.
Illustration: C. granulosum; original, from herbarium material on decaying wood. (A) conidiophores
and conidia; (B) habit on wood; (C) chain of conidia. References (204).
DACTYLOSPORIUM Harz. Conidiophores dark, simple, paler at the tip, bearing conidia successively
on new growing tips; conidia (sympodulospores) brown to subhyaline, ovoid, sometimes inequilateral,
with cross and longitudinal or oblique septa; saprophytic.
Illustration: D. marcopus; redrawn from Hughes (203).
BERKLEASMIUM Zobel. Conidiophores clustered forming a loose sporodochium, dark, short, simple,
each bearing a terminal conidium; conidia (aleuriospores) dark, large, containing many cells irregularly
arranged (dictysporous), oblong to obovoid; saprophytic on decaying wood.
Illustration: B. conkinnum; original, from herbarium material on decayed wood. Reference (293).
SIROSPORIUM Bubak and Serebianikov. Mycelium immersed in leaves or superficial; stroma may be
present; conidiophores arising from hyphae or cells of stroma, simple or branched, brown, each bearing I
to several conidial scars; conidia (sympodulospores) apical, single or successively on new growing tips that
develop to side of previous conidium, subhyaline to brown, phragmosporous or dictyosporous, obovate
to cylindrical, straight or flexuous; parasitic on leaves.
Illustration: S. antenniforme; redrawn from Ellis (118). (A) conidiophore and comdia; (B) mycelium and
conidiophore; (C) conidia.
STIGMELLA Lev. Conidiophores simple, short, upright, composed of several cells or reduced to a peg;
conidia (aleuriospores) dictyosporous, dark, single, apical, globose, elliptical, or cylindrical to obovoid,
cells irregular in shape.
Illustration: S. crataegi; original, from herbarium material on leaves of Crataegus. (A, B) conidiophores
and conidia in section of leaf; (C) conidia. References (113, 199).
DESCRIPTIONS AND ILLUSTRATIONS OP GENERA
DICTYOARTHRINIUM
CONIOSPORIUM
DACTYLOSPORIUM
SIROSPORIUM
BERKLEASMIUM
STIGMELLA
135
136
DESCRIPTIONS AND ILLUSTRATIONS OF GFNERA
HELICOSPORIUM Nees. Conidiophores tall, slender, brown, septate, simple or branched, bearing
conidia apically or laterally; conidia (sympodulosporcs) hyaline to pigmented, septate, coiled; saprophytic
on decaying plant material.
Illustration: Ilelicosporium sp.; original, from culture. Mycelium, conidiophores, and conidia. References
(30,289,290,453).
HFXICOMA Corda. Conidiophores dark, upright, rather stout, septate, mostly simple; conidia
(sympodulospores) hyaline or dark, septate, rather tightly curled; saprophytic on wood and bark.
Illustration: H. muileri; original, from herbarium material on maple wood, (A) conidiophores; (B)
conidia. References (30, 289, 290, 453).
HELICOMIINA Olive. Conidiophores dark, slender, elongate, simple or branched, multiseptate; conidia
(sympodulospores) dark, typically curved or coiled but with some straight conidia, septate, produced
terminally and laterally; parasitic on higher plants. The genus differs from Helicoma in being parasitic and
in producing a large number of straight conidia in addition to curved or coiled one.
Illustration: //. caperoniae; redrawn from Olive (316). (A) conidiophores; (B) conidia.
HELICOON Morgan. Conidiophores long, slender, simple or branched, hyaline or dark; bearing conidia
terminally or laterally; conidia (biastospores or sympodulospores) hyaline or dark, coiled to form an
ovoid or ellipsoid conidium, borne singly; saprophytic on decaying wood.
Illustration: (A) H. auratum; redrawn from Linder (264); (B) H, thaxieri; redrawn from Linder (265).
Reference (289).
XENOSPORIUM Pen/ig. and Sacc. Conidiophores dark, comparatively short and stout, simple or
branched, septate; conidia (aleuriospores) dark, tightly coiled, apical, having both transverse and
longitudinal septa; saprophytic on decaying plant material.
Illustration: X. berke/eyl; redrawn from Linder (264). Mycelium, conidiophores, and conidia. References
(85, 290).
HELICODENDRON Peyron. Conidiophores hyaline, slender, branched, septate, bearing conidia
terminally; conidia (biastospores) subhyaline to brown, coiled to form a large ovoid or ellipsoid spore,
smaller, younger spores formed on the sides of the other spores; saprophytic on decaying plant material.
Illustration: H. gigantium; redrawn from Glen-Bott (146). Mycelium, conidiophores, and conidia.
References (147, 263).
HELICOMYCES Link. Conidiophores hyaline, mostly simple, variable in length; conidia (symposulospores) hyaline or subhyaline, septate, conidial filaments thin, hygroscopic, tightly coiled in one plane;
saprophytic on decaying wood.
Illustration: (A) H. scandens; (B) H. roseus; redrawn from Linder (263). References (221, 289).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
XENOSPORIUM
HELICODENDRON
HELICOMYCES
137
138
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
FLAGELLOSPORA Ingold. Conidiophores long, slender, septate, branched above, ending in phialides
that bear single conidia; conidia (phialospores) hyaline, 1- to several-celled, fiagelliform, slender, curved;
saprophytic on submerged decaying leaves.
Illustration: F penicillioides; redrawn from Ingold (225). (A) portion of conidiophores and conidia;
(B) conidia.
TRISCELOPHORUS Ingold. Submerged, aquatic, with branched, septate mycelium; conidiophores
simple, slender; conidia single, apical, branched, consisting of (1) an elongated main axis continuous with
the conidiophore and (2) elongated branches forming a whorl of 3 slender divergent branches arising from
the lower part of the main axis, hyaline; saprophytic on decayng leaves in water.
Illustration: T. monosporus; redrawn from Tubaki (449). References (224, 327, 328).
LUNULOSPORA Ingold. Conidiophores long, slender, hyaline, branched near the apex, the branches
bearing single conidia apically; conidia (blastospores) hyaline, 1-celled, elongate to filiform, bent, typically
lunate; saprophytic on submerged leaves.
Illustration: L. curvula; redrawn from Ingold (223). (A) conidiophores and conidia; (B) conidia.
References (327, 346).
LEMONNIERA DeWild. Conidiophores hyaline, slender, branched, ultimate branches bearing a few
phialides; conidia apical, hyaline, ultimately septate, with 4 slender, widely divergent arms; saprophytic on
submerged, decaying leaves.
Illustration: L. aquatica; redrawn from Ingold (223). References (228, 346).
VARICOSPORIUM Kegel. No sharp distinction between conidiophores and conidia; conidiophores
simple or sparingly branched near the apex, bearing conidia apically; conidium consisting of a main
elongated axis with 2 or 3 laterals on one side; each lateral is septate and branched again, hyaline;
saprophytic, aquatic or in soil.
Illustration: V. elodeae; redrawn from Ingold (223). Reference (449).
TRICLADIUM Ingold. Conidiophores hyaline, long, slender, branched; conidia single, apical, hyaline,
several-celled, curved, cylindrical, branched, the two branches usually arising from adjacent cells;
saprophytic on submerged decaying leaves.
Illustration: T. splendens; redrawn from Ingold (223). Reference (327).
DICRANIDION Hark. Conidiophores hyaline, single or in loose masses (sporodochium-like), slender,
simple or with a few branches, new growing points produced sympodially; conidia (sympodulospores)
5-celled, produced singly at apex or on new growing points on small denticles; saprophytic on wood.
Illustration: D. fragile; original, from decaying wood and from culture. (A) apical portions of
conidiophores and immature conidia; (B) portion of conidiophore and mature conidium. Reference (97).
INGOLDIA Petersen. Submerged aquatic with septate mycelium; conidia single, apical, hyaline, septate,
consisting of a curved, attenuated axis, two attenuated branches, and a single attenuated secondary
branch; on submerged rotting leaves.
Illustration: I. craginiformis; redrawn from Petersen (327). References (231).
DESCRIPTIONS AND IlLUSTRATlONS OF GtNERA
INGOLDIA
139
140
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
TRIDENTARIA Preuss. Conidiophores hyaline, long, slender, simple, septate, bearing a single conidium
apically; conidia hyaline, trifurcate, rarely 2- or 4-pronged, the basal cell obconidcal, septate, prongs
septate, tapering upward, slightly divergent; parasitic on nematodes or on soil rhizopods, or saprophytic
on decayed wood.
Illustration: 77 implicans; original, from culture isolated from decayed wood. (A) conidiophores and
conidia showing tightly closed prongs as seen in a dry mount; (B) conidiophores and conidium as seen in
water mount; (C) two mature conidia and one very young conidium. References (100, 101).
CULICIDOSPORA Petersen. Conidia single, apical, hyaline, elongate-clavate, 5-celled, subapical cell
swollen and curved, with 2 straight hyphalike branches on the subapical cell and one on the apical cell;
aquatic, on submerged rotting leaves.
Illustration: C. gravida; redrawn'from Petersen (328). (A) conidiophores; (B) conidia.
ACTINOSPORA Ingold. Conidiophore hyaline, slender, septate, upper portion dichotomously branched,
forming apical conidia singly; conidi hyaline, branched, the main body globose or ovoid, with 4 or 5
slender, radiating, septate branched; saprophytic on submerged twigs.
Illustration: A. megalospora; redrawn from Ingold (226).
TETRACHAETUM Ingold. Submerged, aquatic with septate mycelium; conidiophores simple or
sparingly branched, slender; conidia single, apical, hyaline, several-celled, consisting of 4 long branches
diverging from a common point, with one branch of the conidium (before liberation) continuous with the
conidiophore; conidia produced under water, liberated by the breakdown of a special short separating cell.
Illustration: T. elegans; redrawn from Ingold (223). Reference (346).
DENDROSPORA Ingold. Submerged, aquatic with branched, septate mycelium; conidiophores simple,
slender, hyaline; conidia apical, single branched, several-celled, each consisting of one main axis with
several secondary and tertiary branches arising irregularly, hyaline; saprophytic, on decaying leaves in
water.
Illustration: D. erecta; redrawn from Tubaki (449). Reference (87).
ANGUILLOSPORA Ingold. Submerged, aquatic, conidiophores hyaline, slender, simple; conidia single,
apical, slender, several-celled, hyaline, separating from the conidiophore by the breakdown of a special
separating cell at the apex; saprophytic.
Illustration: A. longissima; redrawn from Ingold (223). References (228, 327).
CLAVARIOPSIS DeWild. Conidiophore long, slender, hyaline, simple; conidia hyaline, apical, single,
branched, main axis pyriform, 2-celled, the three branches from the upper cell widely divergent at angles
of about 120°; saprophytic on submerged decaying leaves.
Illustration: C. aquatica; redrawn from Tubaki (449). Reference (223).
TETRACLADIUM DeWild. Conidiophores hyaline, slender, septate, simple or branched in upper
portion; conidia single, apical, hyaline, branched, the main axis narrowly clavate, finally septate, giving
rise to three unequal, divergent, tapering branches; saprophytic on submerged decaying leaves.
Illustration: 77 setigerum; redrawn from Tubaki (449). References (223, 346).
DESCRIPTIONS AND ILLUSTRATIONS Of GENLRA
TRIDENTARIA
ACTINOSPORA
CULICIDOSPORA
ANGUILLOSPORA
A,
CLAVAROPSIS
TETRACLADIUM
141
142
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
ALATOSPORA Ingold. Submerged, aquatic, with branched, septate mycelium; conidiophore simple or
branched near the apex bearing a few phialides; conidia branched, consisting of 4 arms diverging from a
common point; the conidium consisting essentially of a curved main axis (forming two arms) and 2
laterals inserted about the middle of the main axis, apical on the conidiophores, hyaline; saprophytic, on
submerged leaves.
Illustration: A. acuminata; redrawn from Tubaki (449).
THAIXOSPORA Olive. No well developed conidiophores present; conidia develop as direct outgrowths
from branching hyphae, slender, dichotomously branched, many-celled, hyaline, produced in a white mass
inside the ovary of the host; systemic parasitic on higher plants (Veronica peregrina).
Illustration: T. aspera. (A, B) conidia; (C, D) conidia developing from hyphae; redrawn from Olive (316).
ARTICUI.OSPORA Ingold. Conidiophores hyaline, slender, upper part sparingly branched; conidia
hyaline, apical, branched, septate, slender, the three branches slender and about the same diameter as the
main axis; saprophytic on decaying submerged leaves.
Illustration: A. inflata; redrawn from Ingold (225). (A) conidiophores bearing conidia; (B) conidium.
References (327, 346).
DIPLOCLADIELLA Arnaud. Conidiophores erect, producing apical and lateral conidia; conidia
(sympodulospores) consisting of two septate, slender, pointed arms radiating from the basal cells; central
cells dark, apical, and basal cells hyaline; saprophytic.
Illustration: D. scalaroides; redrawn from Tubaki (450). (A) conidiophores with attached conidia; (B)
conidia.
TETRAPLOA Berk and Vr. Conidiophores absent; conidia borne directly on mycelium, each consisting
of 3 to 4 initial cells, each of which develops into a long, attenuated, septate appendage, smooth or rough.
brown; saprophytic.
Illustration: (A, B) T. aristita; (C) 7' eliisii; redrawn from Ellis (112).
SPEIROPSIS Tubaki. Conidiophores erect, simple, straight, septate; conidium single, apical, consisting
of a basal cell and 3 to 5 somewhat divergent arms, each arm consisting of an acropetalous chain of cells,
pale brown.
Illustration: S. pedatospora; redrawn from Tubaki (450).
TRIPOSPERMUM Speg. Conidiophores absent; conidia (blastospores) subhyaline to dark brown,
septate, staurosporous, borne directly on cells of the mycelium and consisting of a stalk and two pairs of
divergent, pointed septate arms; branches not formed simultaneously; saprophytic.
Illustration: T. myrti; original, from culture. (A) stages in development of a conidium from a hypha; (B)
branched conidia. Reference (17, 234).
DESCRIPTIONS A N D ILLUSTRATIONS OF GENERA
ALATOSPORA
THALLOSPORA
ARTICULOSPORA
DIPLOCLADIELLA
SPEIROPSIS
TRIPOSPERMUM
143
144
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
CERATOSPORELLA Hohn. Conidiophores dark, simple, upright, bearing single conidia successively
by protrusion of conidiophore through old conidial scars; conidia (annellospores) dark, composed of 2 or
more septate branches, each arising separately from a basal cell; saprophytic.
Illustration: G stipitata; redrawn from Hughes (201). (A) conidiophores, some with an apical conidium;
(B) conidia. Reference (190).
DICTYOSPORIUM Corda. Conidiophores dark, slender, simple or branched, usually short, bearing a
single branched conidium apically; sometimes arranged in sporodochia; conidia with several close septate
branches arising from different points (branches do not all arise separately from a basal cell); saprophytic.
Illustration: (A) D. toruloides; redrawn from Ellis (125); (B) Dictyosporium sp.; original from material on
decayed wood. References (73, 190).
TRIPOSPORIUM Corda. Conidiophores dark, simple, slender, septate, bearing a single conidium
apically; conidia dark, with three septate arms radiating from a central cell; parasitic on leaves, or
saprophytic on plant material.
Illustration: T. elegans; redrawn from Ellis (125). (A) conidiophores; (B) conidia.
HIRUDINARIA Ces. Mycelium mostly superficial, subhyalinc; conidiophores reduced to short lateral
swellings on the mycelium, brown; conidia consisting of 2 (less often 3) straight or curved arms (horns)
tapering upward, several-celled, dark; parasitic on leaves.
Illustration: H. macrocarpa; original, from herbarium material on Crataegus leaves. (A) much reduced
conidiophores emanating from the mycelium; (B) conidia. Reference (186).
CERATOSPORIUM Schw. Conidiophores consisting of a short cylindrical cell; conidia consisting of
2 or 3 straight or curved arms (horns), tapering upward, several-celled, dark; saprophytic on wood or
bark; near Hirudinaria morphologically.
Illustration: C. fuscescens; redrawn from Hughes (186). (A) mycelium showing short conidiophores and
developing conidia; (B) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
CERATOSPORELLA
DICTYOSPORIUM
HIRUDINARIA
TRIPOSPORIUM
CERATOSPORIUM
145
1 4 6 DESCRIPTIONS AND I L L U S T R A T I O N S OF GtNERA
TUBERCULARIA Tode. Sporodochia rather large, light to orange in color, breaking out through the
bark; conidiophores hyaline, elongate, repeatedly irregularly branched, and bearing conidia terminally;
conidia hyaline, 1-celled, ovoid to elongate in a dry mass on the surface of the sporodochium; mostly
saprophytic on wood.
Illustration: T. vulgaris (Conidial state of Neclria cinnabarina); original, from dried material on twigs. (A)
sporodochia on twig; (B) section through sporodochium; (C) conidiophores and conidia.
HADROTRICHUM Fr. Sporodochia cushion-shaped, dark; conidiophores dark, simple, forming a
palisade and arising from a stromalike layer; conidia dark, nearly spherical, 1-celled, borne singly;
parasitic on leaves; the genus is often placed in the Dematiaceac.
Illustration: IT blasdalei; original, from herbarium material on leaves of Vicia. (A) sporodochia on leaf;
(B) side view of sporodochium; (C) conidiophores and conidia. Reference (205).
ILLOSPORIUM Mart. Sporodochia cushionlike, light colored; conidiophores hyaline, branched,
phialides bearing conidia apically; conidia hyaline, ovoid to oblong, collecting on the surface of the
sporodochium in gelatinous material; parasitic or saprophytic on leaves, frequently as a secondary invader.
Illustration: /. malifoliorum; original, from dried material on apple leaves. (A, B) sporodochia and
masses of conidia; (C) conidiophores and conidia.
STRUMELLA Fr. Sporodochia cushionlike, dark; conidiophores dark, branched; conidia dark, 1-celled,
ovoid or oblong to irregular; parasitic or saprophytic on wood.
Illustration: S. coryneoidea (conidial state of Urnula craterium); original, from herbarium material on
oak. (A) sporodochia; (B) conidia. Reference (76).
HYMENELLA Fr. Sporodochia somewhat flattened or discoid, light colored; conidiophores hyaline,
sparingly to moderately branched, bearing terminal conidia; conidia hyaline, 1-celled, ovoid to oblong,
collecting in a dry mass (not in slime) on sporodochium; saprophytic.
Illustration: H. cerealis; original, from herbarium material on wheat straw. (A, B) sporodochia;
(C) conidiophores and conidia.
SPHAEROSPORIUM Schw. Sporodochia yellowish when fresh, cushion-shaped to hemispherical;
conidiophores short, compact, hyaline, bearing apical chains of conidia; conidia I-celled, globose to ovoid,
large with prominent scars of attachment, hyaline or yellowish; saprophytic on decayed wood.
Illustration: S. lignatile; original, from fresh material on decayed wood. (A, B) sporodochia on wood;
(C) conidiophores; (D) conidia.
DENDRODOCHIUM Bon. Sporodochia cushionlike, light, bursting out of bark; conidiophores hyaline,
verticillately branched; conidia hyaline, I-celled, ovoid to oblong, dry in mass; saprophytic on bark.
Illustration: D. rubellum var. microsporum; original, from herbarium material on bark of Liriodendron.
(A, B) sporodochia on bark; (C) conidiophorc; (D) conidia.
MYROTHECIUM Tode. Sporodochia cushionlike, sometimes with marginal hyaline setae; conidiophores subhyaHne to colored, repeatedly branched, bearing conidia terminally; conidia subhyaline to
dark, 1-celled, ovoid to elongate, dry in mass, parasitic or saprophytic.
Illustration: M. roridum; original, from herbarium material on leaf on Viola. (A) sporodochium;
(B) conidiophores and conidia. References (133, 337, 338, 339, 454).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
TUBERCULARIA
HADROTRICHUM
<? 0
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0
c
o
MYROTHECIUM
147
148
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
TIJBERCUIJNA Sacc. Sporodochia small, breaking out in or near rust pustule; conidiophores hyaline,
simple, bearing single conidia terminally; conidia hyaline, 1-celled, globose or ovoid to irregular; parasitic
on rusts.
Illustration: T. persincia; original, from herbarium material on Euphorbia marginala. (A) section of
sporodochia; (B, C) conidiophores and conidia; (D) aeciospore of rust. Reference (179).
SPHACELIA Lev. Sporodochium stromalike, spreading; conidiophores hyaline, simple, in a compact
palisade; conidia hyaline, small, ovoid, 1-celled, produced in a sugary "honey dew"; parasitic in ovary of
grain; conidial state of Claviceps.
Illustration: S. segetum (Claviceps purpurea); original, from prepared slide. (A) section through young
sclerotium; (B) portion of A, enlarged; (C) palisade of conidiophores and conidia.
VOLUTELLA Tode. Sporodochia discoid, with marginal dark setae; conidiophores usually simple, in a
compact palisade; conidia hyaline, 1-celled, ovoid to oblong; parasitic "or saprophytic.
Illustration: V. frucii; original, from herbarium material on apple fruit. (A) erumpent sporodochia on
apple fruit; (B) conidiophores, conidia and setae.
PUCCINIOPSIS Speg. Sporodochia dark, cushion-shaped; conidiophores dark, simple, in a layer,
bearing conidia apically on successive new growing tips; conidia dark, typically 2-celled, ovoid to oblong;
parasitic.
Illustration: P. caricae; original, from herbarium material on leaves of Carica papaya. (A) sporodochia
on leaf; (B) section of sporodochia; (C) conidiophores and conidia. Reference (266).
RAMULISPORA Miura. Sporodochia small, arising from substomatal stromata and pushing through
stomata; conidiophores hyaline, simple or branched, short; conidia hyaline, filiform, septate, with short
lateral branches, produced in gelatinous material; superficial sclerotia present; parasitic on leaves.
Illustration: R. sorghi; redrawn from Olive et ai (317). Stroma, conidiophores, and conidia in stoma.
EXCIPULARIA Sacc. Sporodochia superficial, scattered, dark, with setae; setae simple, dark, septate,
pointed; conidiophores short, simple, subhyaline; conidia several-celled, dark brown, fusiform, apical,
single; saprophytic.
Illustration: K narsapurensis; redrawn from Subramanian (403). (A) sporodochium; (B) conidia; (C) seta.
BACTRIDIUM Kunze. Sporodochia cushion-shaped to hemispherical, bright-colored (yellow); conidiophores long, simple or branched, hyaline; conidia apical, single, hyaline or containing yellow pigment,
several-celled, very large, cylindrical to long-ellipsoid; saprophytic, on decayed wood.
Illustration: B. flava; original, from fresh material on wood. (A) sporodochium; (B) conidiophores;
(C) conidia.
EXOSPORIUM Link ex Schlech. Mycelium immersed, dark; stromata and sporodochia usually present,
often well developed; conidiophores usually grouped, erect, brown; conidiophore growing out laterally or
obliquely below conidial scar, splitting side wall, then forming new conidium through pore at apex of new
growing point; conidia single, pseudoseptate several-celled, with prominent scar; mostly saprophytic.
Illustration: E. tiliae; (A) sporodochium; (B) conidiophores and conidia; redrawn from Luttrell (272).
Reference (117).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
149
1 50
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
EPICOCCUM Link. Sporodochia dark, more or less cushion-shaped, variable in si?e; conidiophores
compact or loose, dark, rather short; conidia dark, several-celled (dictyosporous), globose; mostly
saprophytic, or weakly parasitic.
Illustration: E. nigrum; original, from fresh material on decayed wood. (A) sporodochia on decayed
wood; (B) conidiophores and conidia. Reference (366).
SPEGAZZINIA Sacc. Sporodochium small, dark; conidia of two kinds: (1) 4-ccllcd, spiny, borne
apically on a long slender conidiophore; (2) 4-celled, smooth, borne on a short conidiophore; saprophytic
on vegetable material; both conidiophore and conidia dark. The smooth conidia and sporodochium are
apparently lacking in some species.
Illustration: S. ornata; redrawn from Bessey (27). Reference (74).
CHEJROMYCES Berk, and Curt. Sporodochium dark; cushionlike to hysteroid; conidiophores dark,
short, simple or branched; conidia dark, branched into three or more upright arms, which do not all arise
from the basal cell; saprophytic on wood. Compare with Dhtyosporium.
Illustration: C. stelhtus; (A) hysteroid sporodochia; drawn from photograph by Damon (71);
(B) original, from herbarium material on decayed wood.
BACTRODESMIl'M Cooke. Conidiophores short, clustered (sometimes into sporodochia), simple or
branched, hyaline to pale brown, narrow at base, septate; conidia several-celled, pale to dark brown,
apical cells often darker, apical, single; saprophytic.
Illustration: Bactrodvsmium sp.; original, from fresh material on decayed wood. (A) habit on wood;
(B) conidiophores bearing conidia emerging from a piece of wood; (C) apical portion of conidiophores
showing conidial attachments. Reference (114).
EVERHARTIA Sacc. and Ellis. Sporodochia somewhat stalked, with an expanded top, dark at the base;
conidiophores slender, hyaline, branched; conidia hyaline, apical, septate, flat, curved or bent; saprophytic
on wood.
Illustration: E. lignatilis; (A) sporodochium; (B) conidiophores and conidia; redrawn from Thaxter
(437). References (263, 289).
HOBSONIA Berk. Sporodochia wartlike, light colored; conidiophores hyaline, slender; conidia hyaline,
many celled, apical, coiled in a loose spiral; saprophytic on plant material.
Illustration: //. mirabilis; (A) portion of sporodochium; (B) conidia redrawn from Under (263). Reference (289).
CAMPTOMERIS Syd. Sporodochia irregular, dark, poorly developed or lacking in some species;.
conidiophores dark, arising from special enlarged cells; conidia dark, 3- or more-celled, elongate, leaf
parasites on Mimosa.
Illustration: C. leuvaenae. (A) sporodochium from above; (B) vertical section through sporodochium;
(C) branch of sporodochium bearing three conidiophores; (D) conidia; redrawn from Bessey (29).
Reference (199).
AECERITA Pers. Stroma covering scale insects; sporodochia somewhat spherical, somewhat colored,
superficial; conidia spherical, 1-celled; on scale insects.
Illustration: A. wehberi; original, from herbarium material on citrus leaf (A) stroma covering scale
insect on citrus leaf; (B) section through stroma; (C) two sporodochia showing sterile hyphae and
conidium-like cells. Reference (131).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
m
EPICOCCUM
SPEGAZZINIA
CHEIROMYCES
BACTRODESMIUM
EVERHARTIA
HOBSONIA
151
152
DESCRIPTIONS AND ILLUSTRATIONS Of GENERA
HETEROCEPHALUM Thaxt. Synncmata with long, cylindrical stalk composed of a central large
strand surrounded by cortical hyphae, fertile head with loose interwoven sterile hyphae and long slender
spinelike hyphae surrounding the spore mass; fertile branches thick, terminating in phialides; conidia
hyaline, small, ovoid; saprophytic on dung or soil.
Illustration: //. auranriacum; (A) young synnema; (B) upper portion of mature synnema; (C) phialides
and conidia; redrawn from Thaxter (437). Reference (301).
STILBUM Tode ex. Fr. Synnemata hyaline or bright-colored, stipe cylindrical, bearing a head of conidia;
conidiophores slender, verticillatefy branched; conidia 1-celled, hyaline, globose to ellipsoid, enveloped in
slime, saprophytic, on bark and wood. Single conidiophores resemble Veriicillium.
Illustration: Stilbum sp.; original, from culture. (A) synncmata showing spores in head of slime;
(B) portion of synnema; (C) single conidiophore; (D) conidia. References (17, 301).
MENISPOROPSIS Hughes. Synnema composed of a central emerging seta and an external shorter
cortex; phialides, pale brown; conidia 1-celled, hyaline, curved, with a short filiform appendage at each
end, produced in slime; saprophytic.
Illustration: M. theobromae; redrawn from Hughes (198). (A) synnema with central seta; (B) conidia.
Reference (301).
ENDOCATYX Berk, and Br. Synnemata expanding upward into a funnel that is filled with conidia;
conidia sessile or on short branches of conidiophore, 1-celled, brown, flattened, ovoid or irregular, with a
germ slit; on twigs.
Illustration: E. thwaitesii; redrawn from Hughes (207). (A) synnemata; (B) conidia. Reference (301).
PESOTUM Crane and Schok. Synnemata mostly erect, simple or branched near base, dark brown to
black, as in Graphium; single conidiophores hyaline, slender, mostly simple; conidia (sympodulospores)
1-celled, hyaline, borne on short blunt denticles; formerly placed in genus Graphium; recently described as
the conidial state of Ceratocystis ulmi.
Illustration: P. ulmi (Graphium ulmi); original from culture. Reference (65).
GRAPHIUM Corda. Synnemata tall, dark, bearing a rounded, terminal mass of hyaline conidia embedded in slime; simple, hyaline conidiophores also produced in abundance, bearing oblong conidia that
reproduce by budding; parasitic, often as vascular pathogens causing wilts of trees, or saprophytic. Some
species are imperfect states of Ceratocystis. Mode of conidial development variable in different species.
Illustration: Graphium sp.; original, from culture obtained from oak wood. (A) habit of synnemata;
(B) synnema and conidial head enlarged; (C) conidiophores and conidia from water mount; (D) short,
hyaline conidiophores and conidia similar to Hyalodendron, Reference (301).
BRIOSIA Cav. Synnemata dark, cylindrical, spore-bearing head ovoid to sub-globose; conidia dark,
1-celled, in chains, collecting in dry masses; parasitic, commonly causing blight of Azalea and
Rhododendron /lower buds.
Illustration: B. azalea; original, from dried material. (A) synnemata on blasted Rhododendron flower;
(B) two synnemata as seen under low magnification; (C) synnema showing sporulating head; (D) conidia.
Reference (301).
DESCRIPTIONS AND IlLUSTRATIONS OF GENERA
GRAPHIUM
BRIOSIA
153
154
DESCRIPTIONS AND ILLUSTRATIONS OF GFNERA
DIDYMOSTILBE P. Henn. Synnemata light, stalk cylindrical, with an expanded, ovoid, or rounded
spore-bearing head; conidiophores hyaline, branched, short conidiophores produced abundantly in
culture, conidia hyaline, 1-cellcd, usually becoming 2-celled, contained in droplets of slime, ovoid to
elongate; saprophytic, principally on wood.
Illustration: Didymostilbe sp.; original, from culture isolated from stump of Liriodendron lulipifera.
(A) synnemata showing heads of conidia embedded in slime; (B) synnema dry; (C) synnema moist;
(D) synnema showing conidiophores, from water mount; (E) branched conidiophore from synnema;
(F) conidia. Reference (301).
ARTHROSPORIUM Sacc. Synnema cylindrical, .subhyaline, with long spore-bearing upper portion;
conidiophores diverging, bearing conidia at apex; conidia mostly 4-celled, hyaline to subhyaline, longfusoid to falcate; saprophytic.
Illustration: S. compositum; original from herbarium material on dead bark. (A) synnema;
(B) conidiophores; (C) conidia. Reference (301).
PODOSPORIUM Schw. Synnemata erect, clustered, black, cylindrical, with a long, apical fertile portion;
conidiophores septate, dark, diverging; conidia several-celled, dark, apical, single.
Illustration: P. rigidum; original, from herbarium material on stems of Ampelopsis quinquefolia.
(A) habit on stem; (B) synnema; (C) conidiophore and conidia. Reference (301).
DENDROGRAPHIUM Massec. Synnema with dark, cylindrical stipe, free ends of hyphae become
conidiophores; conidiophores enlarged, radiating, simple or branched; conidia mostly 4-celled, dark,
apical, in short acropetalous chains, cylindrical-ovoid; saprophytic.
Illustration: D. interseminatum; redrawn from Subramanian (404). (A) synnema with conidia;
(B) enlarged apex of synnema with conidiophores bearing catenulate conidia; (C) conidia. Reference (301).
DORATOMYCES Corda. Hyphae dark; conidiophores dark, solitary or compacted into synnema with
dense, elongated head of conidiogenous cells and chains of conidia, upper part of conidiophores branched
penicillately, producing masses of dry spores apically on conidiogenous cells; conidia (annellospores)
mostly dark, I-celled, ovoid; saprophytic. Similar to Trichurus but without spines.
Illustration: D. stemonitis (Stysanus stemonitis); original, from culture. (A) synnema; (B) separate
conidiophores; (C) conidia. Reference (301, 303).
ISARIOPSIS Fres. Synnemata dark, coposed of loose conidiophores, bearing conidia at or near the tips;
conidia dark or pale, 2- or more-celled, cylindrical to obclavate, often curved; parasitic.
Illustration: /. griseola; original, from herbarium matrcrial on bark. (A, B) synnemata; (C) conidia.
ARTHROBOTRYDM Ces. Synnemata dark, cylindrical, with a globose sporulating head; conidia
hyaline to dark, 3- to 4-celled, produced in slime; saprophytic on wood.
Illustration: A. stilboideum; (A) synnemata; (B) conidiophores; (C) conidia; redrawn from Subramanian
(405). References (195, 301).
DESCRIPTIONS AND ILIUSTRATIONS OF GhNERA
ISARIOPSIS
1 56
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
ISARIA Hers. Synnemata light colored, cylindrical to clavate; conidia hyaline, 1-celled, ovoid, dry, not
produced in gelatinous material; saprophytic or parasitic on insects. Some species are imperfect states
of Cordyceps.
Illustration: /. cretacea; original, from culture. (A) synnemata in culture turning toward source of light;
(B) portion of synnema; (C) conidiophores and conidia. Reference (301).
THAROOPAMA Subram. Synnemata with well-defined stalk and head, hyphae becoming free to form
conidiophores; conidiophores subhyaline to brown, septate, branched 1 to 3 times, with apical hyaline
fertile cells; conidia borne on small denticles, 1-celled, hyaline, globose,
Illustration: T. trina; redrawn from Subramanian (403). (A) synnema; (B) conidiophores and conidia;
(C) conidia. Reference (301).
HARPOGRAPHIUM Sacc. Synnemata dark brown, the upper spore-bearing portion capitate to
elongate, fibrous, the hyphae with thick stubby tips; conidia hyaline, more or less falcate, 1-celled;
saprophytic on bark and wood.
Illustration: //. fascicuhtum; original, from herbarium material on bark. (A, B) synnemata; (C) redrawn
from Subramanian (405). Reference (301).
TRICHURUS Clem, and Shear. Synnemata dark, stalk slender, conidium-bearing portion expanded;
long, black, simple, or branched hairs on spines present among the conidiophores; conidia dark, I-celled,
ovoid, catenulate; saprophytic. Similar to Doratomyces but with spines.
Illustration: T. terrophilus; (A) synnema; (B) portions of synnema showing conidiophores and spines;
(C) conidia; (D) sporogenous cells bearing conidia; original, from culture. References (301, 430).
DIDYMOBOTRYUM Sacc. Synnema with tall, cylindrical stipe and subglobose head, dark; conidiophores divergent, bearing conidia apically; conidia dark at maturity, 2-celled, oblong or cylindrical;
saprophytic.
Illustration: D. cookei: original from herbarium material on dead stems. (A) habit of synnemata on
wood; (B) synnema; (C) conidiophores and conidia. Reference (301).
DESCRIPTIONS AND ILIUSTRATIONS OF GENERA
ISARIA
HARPOGRAPHIUM
DIDYMOBOTRYUM
TRICHURUS
157
158
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
SCLEROGRAPHIUM Berk. Colonies covering surface of leaflets; synnemata tail, slender, black;
conidiophores diverging outward, bearing near the apex small truncate denticles that bear single conidia;
conidia several-celled, dictyosporous, brown, dry.
Illustration: 5". aterrimum; redrawn from Hughes (197). (A) synnema; (B) conidiophores and conidia.
Reference (301).
ACAROCYBE Sydow emend. M.B. Ellis. Mycelium superficial, brown; conidiophores erect, brown,
branched to form tall, slender synnemalike structures, each with a head; synnema forms as hyphae branch
and grows downward, branches closely appressed; head composed of short, thick fertile cells on short
branches; conidia 2- to 3-celled, pale brown, obclavate, straight or curved; on living leaves.
Illustration: A. hansfordii; redrawn from Ellis (115, 120). (A) portions of synnemata showing unusual
form of development; (B) conidiogenous cells; (C) conidia. Reference (301).
SPIROPES Cifcrri. Colonies effused, hairy or velvety, pale to brown or black, often overgrowing and
apparently parasitic on Meliolineae or other tropical leaf ascomycetes; conidiophores simple, single or
clustered into synnemata, pale to dark brown, septate; conidiogenous area simple, sympodular, with
numerous conspicuous conidial scars; conidia solitary, 2- to several-celled, variable but often obclavate,
pale to dark brown.
Illustration: (A) separate conidiophores of 5". capensis; (B) synnema of S. japonicus; redrawn from
Ellis (123).
AKANTHOMYCES Leb. Synnemata light colored, cylindrical or somewhat attenuated above, composed
of compact hyphae; phialides produced as terminal cells of lateral branches in a compact layer, ellipsoid,
obovoid or cylindrical, acute at the apex; conidia hyaline, 1-celled, smooth, catenulate; parasitic on insects
and spiders.
Illustration: A, acuieata; (A) synnemata on dead moth; (B) phialides and conidia; (A) drawn from
photograph; (B) redrawn from drawing; both from Mains (278). Reference (301).
INSECTICOLA Mains. Synnemata light colored, clavate, stipitate, upper fertile portion compact
composed of branching hyphae terminating in phialides that form a compact layer; conidia hyaline,
l-cclled, smooth, catenulate; parasitic on insects.
Illustration: /. clavate; (A) synnemata on infected cricket; (B) phialides and conidia; (A) drawn from
photograph, (B) redrawn from drawing; both from Mains (278). Reference (301).
HYMENOSTILBE Petch. Synnemata nearly cylindrical, composed of longitudinal, closely compacted
hyphae; phialides in a layer covering the synnema, produced on short, lateral branches, subcylindric to
clavate, obtuse or narrowed on short sterigmata; conidia hyaline, 1-celled, smooth, borne singly; parasitic
on insects or spiders.
Illustration: //. verrucosa; (A) synnemata of fungus on spider; (B) conidiophore branch, phialides, and
conidia; (A) drawn from photograph; (B) redrawn from drawing; both from Mains (278). Reference (301).
DESCRIPTIONS AND ILLUSTRATIONS OF GENFRA
SCLEROGRAPHIUM
ACAROCYBE
m
OO
AKANTHOMYCES
SPIROPES
HYMENOSTILBE
INSECTICOLA
159
160
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
GIBELLULA Cav. Synnemata light to brown, cylindrical, composed of loose, longitudinal hyphae;
conidiophores brownish, terminal cell or cells hyaline, apex enlarged, bearing prophialides and phialides
that compose a globose or broadly wedge-shaped head; conidia fusoid to ellipsoid, produced successively,
single or in short chains; parasitic on spiders; conidial states of Torrubiella.
Illustration: G. suffulta; (A) synnemata on mummified spider; (B) portion of synnema showing
conidiophores and comdial heads; (C) single conidiophore and conidial head; (D) portion of conidial
head; (E) phialides; (F) conidia; redrawn from Speare (381). References (277, 301).
HIRSUTELLA Pat. Synnemata, simple or with numerous branches arising nearly at right angles (some
species lack synnemata); phialides arising laterally on synnema or from mycelium on host, hyaline,
inflated below, abruptly or gradually narrowing to long slender sterigmata; conidia hyaline, 1-celled,
oblong to cylindrical, covered with slime; parasitic on insects.
Illustration: H. saussurei. (A, B) portions of synnemata; (C) phialides and conidia; redrawn from Speare
(382). References (135, 279, 286, 301).
SYNNEMATIUM Speare. Synnemata simple or branched, brown when mature; phialides mostly at ends
of branches, slender, tapering to a pointed tip; conidia hyaline to pale brown, covered with slime, several
spores held together in clusters; sclerotia spherical, becoming brown with thick-walled cells; parasitic
on insects.
Illustration: S- jonesii; (A) synnema producing sclerotia; (B) synnema producing conidia; (C) sclerotium
germinating and producing synnemata; (D) phialide and conidium; (E) cluster of conidia in mucus;
(F) sclerotium; redrawn from Speare (382). Reference (279).
DESCRIPTIONS AND I L L U S T R A T I O N S OF GENERA
SYNNEMATIUM
162
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
PHYLLOSTICTA Pers. Pycnidia dark, ostiolate, lenticular to globose, immersed in host tissue,
erumpent or with a short beak piercing the epidermis; conidiophores short; conidia small, 1-celled,
hyaline, ovoid to elongate; parasitic, producing spots, principally on leaves. Compare with Phoma.
Illustration: P. minima; original, from dried material; (A) leaf spot and pycnidia on leaf of maple;
(B) section of leaf and pycnidium; (C) conidiophores; (D) conidia. Reference (52).
/PHOMA Desm. Like Phyllosticta; parasitic, on various plant parts. Both generic names, Phoma and
Phyllosticta, occur commonly in the literature but morphologically they are alike.
Illustration: (A-C) P. hetae, from culture; (D) P. lingam, from section of host; original; (A) side view of
pycnidium; (B) top view of pycnidium; (C) conidia; (D) pycnidium and conidia. Reference (417).
PLENODOMUS Preuss. Pycnidia dark, immersed, irregular in shape, opening irregularly at the apex;
conidia hyaline, 1-celled, oblong; parasitic.
Illustration: P. destruens; original. (A) surface view of erumpent pycnidia on sweet potato stem;
(B) section through pycnidium; (C) pycnidia produced in culture; (D) conidia.
SELENOPHOMA Marie. Pycnidia brown, globose, immersed, erumpent, ostiolate; conidia hyaline,
1-celled, bent or curved, typically lunate or less often boomerang-shaped; parasitic, causing spots on
grasses and some other hosts.
Illustration: S. linicola. (A, B) pycnidia on flax stem, drawn from photographs; (C) conidia; all redrawn
from Vanterpool (457). Reference (386).
PYRENOCHAETA de Not. Pycnidia dark, ostiolate, nearly globose, erumpent with a few simple bristles,
especially near the ostiole; conidiophores simple or rarely branched; conidia small, 1-celled, hyaline, ovoid
to elongate; parasitic or saprophytic.
Illustration: Pyrenochaeta sp.; original, from culture. (A) group of pycnidia; (B) pycnidium;
(C) conidiophores and conidia.
DENDROPHOMA Sacc. Like Phoma and Phyllosticta but conidiophores are branched.
Illustration: D. obscurans; original, from culture. (A, B) pycnidia and exuded masses of conidia;
(C) conidiophores; (D) conidia.
APOSPHAERIA Sacc. Pycnidia dark, rounded, with a short papillate ostiole; conidiophores short,
1-celled, conidia hyaline, 1-celled, elongate to globose; saprophytic on wood.
Illustration: P. pezizoides original, from herbarium material on Fraxinus wood. (A) habit of pycnidia;
(B) section through pycnidia; (C) conidiophores; (D) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
SELENOPHOMA
i I
163
164
DESCRIPTIONS AND ILLUSTRATIONS OF GtNtRA
PEYRONELLAEA Goidanich. Pycnidia brown to black, superficial to partly immersed, rounded, with
conspicuous ostiole, single to crowded; conidia 1-celled, hyaline or later becoming subhyaline to dark,
ovoid to ellipsoid; chlamydospores many-ceiled, dark, apical or intercalary, with irregular septations;
saprophytic or parasitic.
Illustration: Peyronellaea sp.; original, from culture. (A) habit of pycnidia in culture; (B) pycnidia;
(C) conidia; (D) chlamydospores. References (150, 443).
RHIZOSPHAERA Mang. and Har. Pycnidia superficial, somewhat globose, dark, of cellular texture,
with ostiole at apex, tapering below to a stalk; conidiophores short, simple; conidia 1-cellcd, hyaline,
ovoid, smooth.
Illustration: R. pini; original, from herbarium material on leaves of Abies balsamea. (A, B, C) habit of
pycnidia on leaf; (D) pyenidium; (E) conidiophores and conidia.
^PHOMOPSIS Sacc. Pycnidia dark, ostiolate, immersed, erumpent, nearly globose; conidiophores
simple; conidia hyaline, 1-celled, of two types, ovoid to fusoid (alpha) conidia, and filiform, curved or bent
(beta conidia); parasitic, causing spots on various plant parts. Imperfect state of Diaporthe.
Illustration: P. (Diaporthe) vexans; original, from egg plant fruit. (A) fruit spot showing pycnidia;
(B) pycnidia; (C) alpha conidia; (D) beta conidia; (E) conidiophores. References (340, 342).
ASTEROMELLA Pass, and Thum. Pycnidia dark, small, globose, ostiolate, located in a mass of
radiating dark hyphac (subiculum); conidia hyaline; l-cellcd, ovoid to cylindrical; parasitic on leaves.
Illustration: A. andrewsii; original, from herbarium material on leaves of Gentiana puberula. (A) leaf
spots and habit of fungus; (B) lop view of pycnidia and radiating hyphae; (C) section of pyenidium;
(D) conidia.
CHAETOPHOMA Cooke. Pycnidia dark, small, globose to irregular, without ostiole, in dense or loose
clusters, seated on an olive-colored subiculum; conidia hyaline, I-celled, very small, ovoid; saprophytic on
plant material.
Illustration: C. confluens; original, from herbarium material on dead stems of Spartina. (A) habit,
showing clusters of pycnidia on stem; (B) group of pycnidia, enlarged; (C) conidia.
- MACROPHOMA Berl. and Vogl. Pycnidia dark, ostiolate, globose, erumpent; conidiophores simple,
short or elongate; conidia hyaline, 1-celled, over 15 microns long, ovoid to broadly ellipsoid; parasitic; may
be a stage in the development of Botryodiplodia or DothiorellaAncludcd here because the name
commonly occurs in the literature.
Illustration: Macrophoma sp.; original, from dried oak leaves. (A) leaf spot and pycnidia; (B) section
through pyenidium; (C) conidiophores and immature conidia; (D) mature conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
A
00
Oo
^
C
E
PEYRONELLAEA
RHIZOSPHAERA
ASTEROMEUA
MACRO PHOMA
CHAETOPHOMA
165
166
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
NEOTTIOSPORA Desm. Pycnidia separate, globose, membranous; dark, innate, ostiolate; conidiophores short, simple, hyaline; conidia 1-celled, hyaline, each with a single appendage; appendage mucoid,
evanescent, in the form of an inverted, hollow cone with thin, hyaline walls, formed by the rupture of the
outer wall, which later becomes everted and funnellike; saprophytic.
Illustration: N. caricina; redrawn from Cunnell (67). (A) section of pycnidium; (B) conidiophores
showing developing conidia; (C) conidia with appendages. Reference (413).
CYTOSPORINA Sacc. Stroma black, cushion-shaped or tubercular; pycnidia distinct, sunken, arranged
more or less in a circle in the stroma, with ostiole; conidia 1-celled, hyaline, filiform, curved or bent;
saprophytic on bark.
Illustration: C. ludibunda; original, from herbarium material on bark of Prunus serrulata. (A) habit of
pycnidia in bark; (B) section through stroma and pycnidia; (C) conidia.
SCEEROTIOPSIS Sperg. Pycnidia large, separate, smooth, without a pore, fleshy or membranous;
conidiophores erect, simple, filiform; conidia 1-cclled, hyaline, ellipsoid, angular at both ends.
Illustration: S. concava; original, from herbarium material on Galas aphylla leaf. (A) habit of pycnidia
on leaf; (B) section of pycnidium; (C) conidiophores; (D) conidia.
AMPELOMYCES Ces. (Cicinnoholus Ehrenb.) Pycnidia dark, rounded, clavate or fusoid, developing
inside conidiophores of powdery mildew fungi (Erysiphaceae), without ostiole; conidia hyaline or
subhyaline to dark, 1-celled, ovoid to oblong; parasitic on Erysiphaceae.
Illustration: A. quisqualis; original, from herbarium material on Erysiphe on leaf of Grindelia.
(A) hyphae and conidiophores of Erysiphe, some bearing pycnidia of the parasite; (B, C) pycnidia
enlarged; (D) conidia. References (270, 356).
DILOPHOSPORA Desm. Pycnidia dark, globose, ostiolate, usually stromatic, within plant tissue;
conidia 1-celled, hyaline, cylindrical, with short, branched slender appendages at both ends.
Illustration: D. alepecuri; original, from herbarium material on Andropogon trachycaulum. (A) habit of
pycnidia in leaf; (B) pycnidia in stroma; (C) conidia with appendages.
— DOTHIORELLA Sacc. Pycnidia dark, globose, grouped in a well-developed stroma; stroma subcortical,
breaking out; conidiophores simple, short; conidia hyaline, 1-celled, ovoid to broadly ellipsoid; parasitic or
saprophytic on wood.
Illustration: Dothiorella sp.; original, from dried material on oak twigs. (A) habit of pycnidia and
stromata; (B) section through stroma; (C) conidiophores; (D) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
NEOTTIOSPORA
CYTOSPORINA
(f ^ J
B
C
SCLEROTIOPSIS
AMPELOMYCES
DILOPHOSPORA
DOTHIORELLA
I
67
168
DESCRIPTIONS AND ILLUSTRATIONS OF GF.NFRA
ELEUTHEKOMYCELLA Hohn. Pycnidia single, black, smooth, soft-leathery, with ostiole; conidiophores simple or branched, septate; conidia 1-celled, hyaline, cylindrical-ellipsoid, with a filiform pedicel
and a slender, apical appendage; on other fungi.
Illustration: E. mycophila; redrawn from Seeler (367). (A) pycnidium embedded in host fungus; (B) cells
of pyenidial wall, (C) conidiophores and conidia.
SPHAERONAEMA Fr. Pycnidia dark, superficial or crumpent, base spherical, with a long beak;
conidiophores simple; conidia hyaline, 1-celled, ovoid to elongate; chiefly saprophytic.
Illustration: S. acerinum; original, from herbarium material on dead braches of Acer. (A) habit of
pycnidia; (B) section showing single pycnidium enlarged; (C) conidiophores, conidia, and sterile hyphae;
(D) conidia.
HYALOPYCNIS Hohn. Pycnidia superficial, light-colored (shiny white) membranous, with a globose
base and a long, subcylindrical neck, fimbriate at the apex; wall of pycnidium and neck composed of
parallel hyphae fused laterally; conidiophores long, simple or branched; conidia 1-celled, hyaline,
cylindrical or ovoid; on other fungi.
Illustration: Hyalopycnis sp.; original, from culture. (A) habit of pycnidia in culture; (B) pycnidium
showing parallel hyphae; (C) conidiophore; (D) conidia from pycnidium; (E) conidia borne directly on
mycelium. Reference (326).
EEEUTHEROMYCES Fuckel em. Seeler. Pycnidia single, superficial, light-colored, soft leathery or
gelatinous and translucent when wet, walls and neck composed of small irregular cells; conidiophores
hyaline, lining neck as well as base of pycnidium, septate, bearing conidia apically and laterally; eonidium
1-celled, hyaline, ellipsoid, attenuated at apex and at base; on basidiomycetes.
Illustration: E. subulatus; redrawn from Seller (367). (A, B) pycnidia; (C) cells of pyenidial wall; (D)
conidiophores; (E) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
B
f
\
C
ELEUTHEROMYCELLA
SPHAERONAEMA
ELEUTHEROMYCES
HYALOPYCNIS
169
170
DESCRIPTIONS AND ILLUSTRATIONS OT GENERA
PEEUROSTROMELIA Petr. Pycnidia tufted thickly or hairy, on stroma, with or without ostioles;
conidiophores long, simple or branched, septate; conidia 1-celled, hyaline, borne at the apex and on sides
at the septa of the conidiophore.
Illustration: P. deiitiscens; original, from herbarium material on bark of Primus. (A) habit of pycnidia in
bark; (B, C) sections of stroma and pycnidia; (D) conidiophores; (E) conidia.
FUSICOCCUM Corda. Pycnidia in spherical or flattened, subepidermal, erumpent, dark stroma, one to
several per stroma; opening separately or with a common pore; conidiophores simple, short; conidia
hyaline. I-celled, fusoid; parasitic or saprophytic on wood.
Illustration: E Uicinum; original, from herbarium material on dead branch of flex opaca. (A) habit of
pycnidia; (BJ section through stroma and pyenidium; (CJ conidiophores and conidia; (D) conidia.
RABENHORSTIA Fr. Pycnidia borne in black, erumpent, subcortical stroma; stroma nearly globose,
wider at base, upper part truncate, often circularly split at the top, divided into several cavities;
conidiophores filiform, simple, septate; conidia hyaline, 1-celled, ovoid to oblong; saprophytic
on branches.
Illustration: R. tiliae; original, from herbarium material on dead branch of Tilia. (AJ habit of pycnidia;
(B) section through stroma; (C) conidiophores; (D) conidia.
^
vtCYTOSPORA Ehrenb. Pycnidia within a superficial or erumpent, tuberculate, globose, stroma; cavities
irregular, incompletely separate; conidiophores slender; conidia hyaline, 1-celled, elongate-curved
(allantoid); parasitic, or saprophytic on wood. Mostly imperfect states of Vaha.
Illustration: C. (Vaha) leucosioma; original, from herbarium material on twigs of Prunus domestica.
(A) habit of stromata; (B) section through stroma; (C) conidiophores; (D) conidia.
CYTOSPORELEA Sacc. Pycnidia forming irregular cavities within erumpent, tuberculate stroma;
conidiophores slender, simple or branched; conidia hyaline, 1-celled, ovoid to oblong; parasitic or
saprophytic on wood; similar to Cytospora except for shape of conidia.
Illustration: C. carnea; original, from herbarium material on dead twigs of Castanet* deniata. (A) habit
of stromata; (B) section through stroma; (C) conidiophores and conidia.
DESCRIPTIONS AND ILLUSTRATIONS Of- GFNLRA
'^fs
FUSICOCCUM
PLEUROSTROMELLA
CYTOSPORA
CYTOSPORELLA
17
172
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
SPORONEMA Desm. Pycnidia subepidermal, slightly membranous, at first closed, later dehiscing
radiately, gaping, dark; conidiophores slender, typically branched; conidia 1-celled, hyaline, ovoid to
oblong; on leaves.
Illustration: S. phacidioides; redrawn from Jones (241). Reference (262).
CATINULA Lev. Pycnidia mostly globose-ovoid, dark, superficial, membranous-leathery, rather firm
and solid, or somewhat fleshy when wet, nearly smooth, gaping at the top with a large mouthy often
brightly colored when fresh; conidiophores simple or branched; conidia 1-celled, subhyaline, globose
to oblong.
Illustration: C. thujae; original, from herbarium material on Thuja plicata. (A) habit of pycnidia on
leaves; (B) pycnidium; (C) conidiophores; (D) conidia.
AMEROSPORIUM Speg. Pycnidia superficial, subcupulate, opening wide at apex, black, surrounded
by long, pointed, black setae; conidiophores crowded, branched; conidia 1-celled, hyaline to subhyaline,
without bristles, cylindrical to ellipsoid; saprophytic.
Illustration: A. caricum; original, from herbarium material on Carex leaves. (A) habit of pycnidium on
leaf; (B) pycnidium; (C) seta; (D) conidiophore; (E) conidia.
SHANORIA Subram. and Ramakr. Stromata black, carbonaceous, with one or more locules, lined with
conidiophores, at maturity dehiscing by an irregular longitudinal rupture; conidiophores simple,
cylindrical or clavate; conidia 1-celled, hyaline, with a filiform subapical appendage at each endIllustration: S. bamhusarum; redrawn from Shanor (368). (A) habit of stromata in leaf; (B) section
through stroma and pycnidia; (C) conidiophores and conidia. References (412).
DOTHICHIZA Lib. Pycnidia subglobose, smooth, dark, erumpent from bark, somewhat disc-shaped,
irregularly dehiscent; conidiophores simple, slender; conidia 1-celled, hyaline, ovoid to cylindrical.
Illustration: D. populae; original, from herbarium material on Populus sp. (A) habit of pycnidia on
wood; (B) section of pycnidium; (C) conidiophores; (D) conidia.
DINEMASPORIUM Lev. Pycnidia black, cup-shaped, superficial, with long dark setae; conidiophores
rod-shaped, mostly simple; conidia hyaline, I-celled, elongate or allantoid, with a slender appendage at
each end; saprophytic.
Illustration: Dinemasporium sp.; original, from fresh material on dead grass stem. (A) habit of pycnidia;
(B) side view of pycnidium; (C) top view of pycnidium, enlarged; (D) seta; (E) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENtRA
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DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
ANTHASTHOOPA Subram. and Ramakr. Pycnidia immersed, with membranous wall, without stroma;
conidiophores produced from surface of a cushion-shaped mound of tissue at base of pycnidial cavity;
conidia f-celled, hyaline, concave-convex in outline, each with an apical, hyaline, mucoid appendage
turned backwards and closely appressed to the concave side of the conidium; saprophytic.
Illustration: A. simba; redrawn from Subramanian and Ramakrishnan (410). (A) section through pycnidium; (B) conidia with appendages.
HAINESIA Ellis and Sacc. Pycnidia fleshy to gelatinous, bright-colored, globose at first, opening and
becoming discoid, erumpent; conidiophores long, slender, branched; conidia hyaline; l-celled, oblong to
fusoid or somewhat allantoid; saprophytic.
Illustration: H. rubi; original, from herbarium material on leaves of cultivated Rubus. (A) habit of
pycnidia; (B) section through open pycnidium; (C) conidiophores and conidia.
ASCHERSONIA Mont. Pycnidia in brightly colored, hemispherical or cushion-shaped stromata,
somewhat sunken, opening by wide pores or ruptures that join to form irregular cracks; conidiophores
slender, branched; conidia hyaline, usually 1-cclled, but sometimes reported as being septate, fusoid;
saprophytic or some species parasitic on insects.
Illustration: A. aleyrodis; original, from herbarium material on Aleyrodes citri on leaves of citrus.
(A) habit of stromata covering insects; (B) section through stroma and pycnidia; (C) conidiophores;
(D) conidia.
ACTINOPELTE Sacc. Pycnidia superficial, borne on a stalk or columella, dimidiate, shield-shaped,
black, coalescing or scattered, ostiole variable; conidiophores simple; conidia hyaline, less often brownish,
I-celled, ovoid, oblong or fusoid; parasitic on leaves.
Illustration: A. (I\eptothyrium) dryina; original, from fresh material on leaves of Quercus coccinea.
(A) habit of pycnidia in leaf spot; (B) pycnidium, top view; (C) pycnidium, lower surface showing
conidiophores and conidia; (D) conidiophores and conidia. Reference (435).
MELASMIA Lev. Pycnidia in a broad, black, flattened stroma that is superficial or nearly so, dimidiate;
conidiophores simple or branched; conidia hyaline or subhyaline, i-celled, allantoid or fusoid; parasitic on
leaves; imperfect state of Rhytisma.
Illustration: M. hypophylla; original, from herbarium material on leaves of Gleditsia triacanthos.
(A) habit of pycnidia; (B) section through pycnidium; (C) conidiophores; (D) conidia.
LEPTOTHYRIUM Kunze. Pycnidia superficial or erumpent, dimidiate, shield-shaped, dark, with or
without ostiole; conidiophores simple; conidia hyaline, l-celled, ovoid, oblong or curved; parasitic on
leaves, fruit, etc.
Illustration: L. lonicerae; original, from herbarium material on leaves of Lonicera invoiucrata.
(A, B) habit of pycnidia; (C) pycnidium breaking open; (D) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
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DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
LEPTOSTROMA Fr. Pycnidia black, separate, dimidiate, subsuperficial, flattened to elongate, more or
less cleft lengthwise; conidiophores short, simple, 1-celled; conidia hyaline, 1-celled, ovoid, elongate or
allantoid; parasitic or saprophytic; probably imperfect state of Hysteriaceae.
Illustration: L. actaea; original, from herbarium material on Cimicifuga racemosa. (A) habit of pycnidia;
(B, C) pycnidia enlarged; (D) section of pycnidium; (E) conidiophores and conidia.
CONIOTHYRIUM Sacc. Pycnidia black, globose, separate, erumpent, ostiolate; conidiophores short,
simple; conidia small, dark, 1-celled, ovoid or ellipsoid; parasitic or saprophytic.
Illustration: Coniothyrium sp.; original, from fresh material on rose stems and culture obtained from rose.
(A) habit, necrotic spot, and pycnidia; (B) pycnidia in culture; (C) conidiophores and conidia.
HARKNESSIA Cooke. Pycnidia globose, conical, thin, white, porous-lacerate at the apex, bursting out
through the leaf tissue; conidiophores filiform; conidia dark, 1-celled, ellipsoid to ovoid, drawn out into a
hyaline pedicel (conidiophore); saprophytic on leaves.
Illustration: H. eucalypti; original, from herbarium material on Eucalyptus leaves. (A) habit of pycnidia;
(B) top and side views of pycnidia enlarged; (C) section through pycnidium; (D) conidiophores and
conidia. Reference (422).
CHAETOMELIA Fuckel. Pycnidia black, superficial, separate, without ostiole, covered sparsely with
dark bristles; conidiophores simple or branched; conidia dark to subhyaline, 1-celled, fusoid to somewhat
curved; saprophytic.
Illustration: C aira; original, from herbarium material on dead stalks of Sorghum vulgare. (A) habit of
pycnidia; (B) pycnidium enlarged; (C) bristle; (D) conidiophore and conidia; (E) pycnidium of
Chaetomella sp. from culture. Reference (358).
SPHAEROPSIS Sacc. Pycnidia black, separate or grouped, globose, erumpent, ostiolate; conidiophores
short; conidia large, dark, 1-celled, ovoid, elongate or somewhat irregular; parasitic.
Illustration: S. malorum (Physalospora obtusa); original, from herbarium material on apple leaf, fruit,
and from culture. (A) pycnidia in leaf spot; (B) section of pycnidium in fruit; (C) conidia from culture.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
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DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
HAPLOSPOREIXA Spcg. Pycnidia clustered in a black, wartlike stroma that bursts out of the bark,
papillate; conidiophores simple; conidia large, dark, l-celled, ovoid or oblong; parasitic or saprophytic.
The genus may be synonymous with Sphaeropsis, but the latter is described as having no stroma.
Illustration: H. longipes; original, from herbarium material on dead limbs of Morus alba. (A) habit of
pycnidia and stromata; (B) section through stroma; (C) conidiophores, conidia, and sterile hyphae;
(D) conidia.
RHYNCHOPHOMA Karst. Pycnidia separate, not on leaves, somewhat globose, beaked, bursting out of
substrate (usually bark) or superficial, opening by a large pore; conidiophores simple or branched; conidia
2-celled, hyaline, ovoid-oblong.
Illustration: R. raduloides; original, from herbarium material on stems of Ribes hracteosum (A) habit of
pyenidium in bark; (B) section of pyenidium; (C) conidiophores; (D) conidia,
ASCOCHYTA Lib. Pycnidia dark, globose, separate, immersed in host tissue, ostiolate; conidia hyaline,
2-celled, ovoid to oblong; parasitic, principally causing leaf spots. Much like Phyllosticta but with 2-cclled
conidia.
Illustration: Ascochyta sp.; original, from fresh and dried material on barly leaf. (A) habit of pycnidia in
leaf spot; (B, C) top and side views of pycnidia; (D) conidia. Reference (343).
DIPLODINA Westend. Pycnidia black, separate, immersed or erumpent, globose or flattened, ostiolate;
conidiophores simple, slender; conidia hyaline, 2-celled, ovoid or ellipsoid; parasitic or saprophytic;
similar to Ascochyta but not produced in spots.
Illustration: D. macrospora; original, from herbarium material on dead twigs of Cornus. (A) habit of
pycnidia; (B) section through pyenidium; (C) conidiophores; (D) conidia.
DARLUCA Cast. Pycnidia black, spherical, ostiolate, superficial, located in rust sori; conidia hyaline,
2-celled, ellipsoid or fusoid to oblong, tipped with mucous or bristlelike appendages at both ends; parasitic
on rust fungi, chiefly on uredia.
Illustration: D.filum; original, from dried material of Puccinia on grass leaf. (A, B) habit of pycnidia in
uredia; (C) section through uredium of rust showing pycnidia; (D) conidia.
KELXERMANNIA Ellis and Everh. Pycnidia black, globose, separate, immersed in host tissue,
ostiolate; conidiophores short, simple; conidia hyaline, mostly 2-celled, cylindrical with an awl-shaped
appendage at the tip; parasitic or saprophytic.
Illustration: K. yuccaegena; original, from herbarium material on Yucca angustifolia. (A) habit of
pycnidia; (B) section of Yucca leaf showing location of pycnidia; (C) section of pyenidium;
(D) conidiophores; (E) conidia.
ROBILLARDA Sacc. Pycnidia brown to pale, in spots, erumpent to subsuperficial, globose to flattened,
with small ostiole; conidia hyaline, 2-celled, cylindrical, with 3 to 4 hyaline setae at one end; parasitic on
grasses, causing leaf spots.
Illustration: R. phragmites; redrawn from Cunnel (69). (A, B) pycnidia; (C) conidia with appendages.
References (305, 385, 386).
DESCRIPTIONS AND ILLUSTRATIONS OF GENCRA
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DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
-DIPLODIA Fr. Pycnidia black, single, globose, immersed, erumpent, ostiolate; conidiophorcs slender,
simple; conidia dark, 2-celled, ellipsoid or ovoid; parasitic or saprophytic.
Illustration: D. zeae; original, from herbarium material on dead corn stalk and from culture. (A, B) habit
of pycnidia; (C) pyenidium from culture; (D) conidia.
BOTRYODIPLODIA Sacc. Pycnidia black, ostiolate, erumpent, stromatic, confluent; conidiophorcs
simple, short; conidia dark and 2-celled at maturity, ovoid to elongate; parasitic or saprophytic on twigs.
This genus is much like Macrophoma or Dothiorella, if only immature conidia are present.
Illustration: B. acerina; original, from herbarium material on twigs of Acer. (A, B) habit of pycnidia and
stromata; (C) section through pyenidium; (D) conidiophorcs; (E) conidia.
HENDERSONULA Spcg. Pycnidia black, stromate, 1 to several per stroma, locules occurring at
different levels in stroma; conidiophores long, flexuous; conidia often extruded in cirri; at first 1-celled,
hyaline to yellowish, later becoming 3- to 4-celled and dark; parasitic or saprophytic on wood or bark.
Illustration: Hendersonula sp.; original, from material from pine bark. (A) stroma bearing pycnidia
breaking through bark; (B) section through stroma showing pycnidia; (C) immature conidia; (D) mature
conidia.
STAGONOSPORA Sacc. Pycnidia dark, separate, superficial or erumpent, globose, ostiolate; conidiophores short; conidia hyaline, typically 3- to 4-celled, cylindrical to elliptical; parasitic or saprophytic on
leaves and stems.
Illustration: S. carpathica; original, from herbarium material on leaves of Trifolium repens. (A, B) habit
of pycnidia; (C) section through pyenidium; (DJ conidiophores; (EJ conidia. Reference (68).
ARISTATOMA Tehon. Pycnidia brown, globose, erumpent, ostiolate, separate, bearing dark brown
setae near the ostiole; conidiophores short, simple; conidia hyaline, several-celled, cylindrical; parasitic,
causing leaf spots.
Illustration: A. oeconimicum; original, from herbarium material on leaves of Vigna sinensis.
of pycnidia; (C) section through pyenidium; (D) conidia. Reference (418).
(A, B) habit
DOTHISTROMA Hulbray. Stroma dark, elongate, innate, becoming erumpent and swollen, with a stalk
extending into the substratum, composed internally of dense, vertical hyphae; locules separate, one to
several in the upper part of the stroma; conidiophores simple, slender; conidia several-eel led, hyaline,
long-cylindrical to filiform; on pine needles.
Illustration: D. pini; original, from herbarium material on needles of Pinus nigra. (A) habit of pycnidia
on pine needle; (B) section through stroma and pyenidium; (C) conidia. Reference (216).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
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DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
DISCOSIA Lib. Pycnidia black, separate, circular, flattened, between the epidermis and cuticle;
conidiophores short, simple; conidia hyaline, several-celled, allantoid to fusoid, with single appendage at
each end; parasitic.
Illustration: D. maculicila; original, from herbarium material on Smilex leaves. (A) habit of pycnidia;
(B) single pyenidium, top view; (C) section of pyenidium; (D) conidiophores and conidia. Reference (163).
BARTILINIA Tassi. Pycnidia dark, globose, separate, ostiolate, innate or erumpent; conidiophores
short; conidia hyaline, usually 4-cclled, the lower cell tapering, appendages delicate, arising from apical
cell, usually 3 or 4; saprophytic.
Illustration: B. nolinae; (A) top view of pyenidium; (B) section through pyenidium; (C) conidia; drawn
from photographs from Pollack (336).
TETRANACRIUM Hudson and Sutton. Pycnidia immersed, hysteriform; conidiophores erect, simple,
hyaline, arising from inner cells of pyenidium; conidia single, apical pale brown, branched, composed of 4
divergent branches, all arising from a globose basal cell; the main upright branch often somewhat longer,
the side branches equal, each branch 3- to 5-celled; saprophytic.
Illustration: T. gramineum; redrawn from Husdon and Sutton (181). (A) section through pyenidium; (B)
conidiophore and developing conidium; (C) conidium.
MICROPERA Lev. Pycnidial cavities in yellowish to dark, waxy, erumpent stroma, opening irregularly,
with one or more irregular cavities; conidiophores simple or branched; conidia hyaline, septate, elongatefiliform, pointed at the ends; frequently sickle-shaped; parasitic or saprophytic.
Illustration: M. abietina (Dermea balsamea); original, from fresh material on branches of Tsuga canadensis.
(A) habit of stromata; (B) section through stroma showing pycnidial cavities; (C) conidiophore
and conidia.
^SEPTORIA Sacc. Pycnidia dark, separate, globose, ostiolate, produced in spots, erumpent; conidiophores short; conidia hyaline, narrowly elongate to filiform, several-celled; parasitic, typically causing
leaf spots.
Illustration:S. apii; original, from dried material on leaves of Apium. (A) habit of pycnidia; (B) section
through pyenidium; (C) conidiophores and conidia.
GELATINOSPORIUM Peck. Pycnidia stromatic, arising from a dark hypostroma, splitting open
irregularly, tissue cartilaginous; conidiophores simple or branched; conidia hyaline, I- or more-celled,
narrowly spindle-shaped, bowlike, both ends pointed; spraophytic on branches.
Illustration: G. hetulinum; original, from herbarium material on BetuJa lenta. (A, B) habit of pycnidial
stroma; (C) section of stroma; (D) conidiophores and conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
TETRANACRIUM
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DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
EPHELIS Fr. Stroma dark, or lighter when young, resembling unopened smut galls; pycnidia erumpent,
open cupulate, somewhat gelatinous; conidia hyaline, 1-celled, acicuiar; parasitic on grasses; conidial
states of Bahnsia.
Illustration: E. (Balansia) horealis; original, from herbarium material on stems of grass. (A) stroma and
pycnidia; (B) pycnidia enlarged; (C) conidia. Reference (94).
HENDERSONIA Sacc. Pycnidia dark, separate, globose, ostiolate, immersed, usually erumpent; conidia
dark, several-celled, elongate to fusoid; saprophytic or parasitic.
Illustration: H. celtifoUa; original, from herbarium material on leaves of Celtis occidentaHs. (A) habit of
pycnidia; (B) section through pycnidia; (C) conidia.
LEPTOSTROMELLA Sacc. Pycnidia black, elongate, longitudinally cleft, at first covered and at
maturity appearing superficial, flattened to depressed; conidiophores simple, short; conidia hyaline, 1- to
several-celled, elongate to filiform; saprophytic.
Illustration: L. filicina; original, from herbarium material on dead leaf stalks of Dry op ten's spinulosa.
(A, B) habit of pycnidia; (C) section through pyenidium; (D) conidiophores and conidia.
PHAEOSEPTORIA Speg. Pycnidia dark, spherical, separate, ostiolate, subepidermal or erumpent;
conidiophores simple, short; conidia yellowish to light brown, elongate to filiform, several-celled; parasitic
principally on grasses.
Illustration: P. festucae var. muhlenbergiae; original, from culture obtained from Muhlenbergia.
(A) pyenidium; (B) conidiophores and immature conidia; (C) mature conidia. Reference (384).
SPHAEROGRAPHIUM Sacc. Pycnidia black, separate, base globose, beak conical, spinelike, erumpent;
conidiophores branched; conidia hyaline, I- to 2-celled, filiform-fusoid, often curved; saprophytic.
Illustration: S. fraxini; original, from herbarium material on twig of Fraxinus. (A) habit of pycnidia;
(B) single pyenidium; (C) conidiophores and conidia.
RHABDOSPORA Mont. Pycnidia dark, separate, not produced in spots, erumpent, ostiolate; conidiophores short, simple; conidia hyaline, narrowly elongate to filiform, several-celled parasitic or saprophytic.
Illustration:/?, solidaginis; original, from herbarium material on stem of Solidago canadensis.
(A, B) habit of pycnidia; (C) section through pyenidium; (D) conidia.
CHAETOSEPTORIA Tehon. Pycnidia complete, separate, spherical, innate, without clypeus, subicle or
stroma, with ostiole, without beak, crowned with setae; conidia long, slender, several-celled, hyaline,
parasitic on leaves, in spots.
Illustration: C. wellmanii; redrawn from Yerkes (479). (A, B) pycnidia; (C) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
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DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
PHLYCTAENA Mont, and Desm. Pycnidia dark, separate or sometimes confluent, developing in or
under the epidermis or bark, closed or ostiolate, usually with one chamber or divided by irregular folds;
conidiophores simple or forked; conidia hyaline, 1-celled, cylindrical or long, spindle-shaped, mostly bent,
sickle-shaped; saprophytic.
Illustration: P. albocincta; original, from herbarium material on stem of Rhus radkans. (A) habit of
pycnidia; (B) section through pyenidium; (C) conidiophores; (D) conidia.
PROSTHEMIUM Kunze. Pycnidia separate, covered, later breaking out, carbonaceous, globosedepressed, opening by a pore, dark; conidiophores filiform, hyaline, septate, conidia .several-celled, dark,
cylindrical to ellipsoid, stellately joined into few-spored groups, resembling a staurospore.
Illustration: P. hetulinum; original, from herbarium material on bark of Betula alba. (A) habit of
pycnidia in bark; (B) section of pyenidium; (C) conidia.
CHONDROPODIUM Hohnel. Pycnidia stromatic, stalked, columnar, externally black, hard, internally
gelatinous, conidiophores simple, conidia hyaline, several-celled, crescent-shaped or sickle-shaped; weakly
parasitic or saprophytic.
Illustration: C. pseudotsugae. (A) habit of pycnidia; (B) section through pyenidium; (C) conidiophores
and conidia; (A, B) drawn from photographs; (C) from drawing. All redrawn from White (470).
PHLEOSPORA Wallr. Pycnidia dark, imperfectly formed, globose, innate in tissue, not in distinct spots;
conidia hyaline or subhyaline, several-celled, elongate fusoid to filiform; parasitic or saprophytic.
Illustration: P. robinae; original, from herbarium material on leaves of Robiniapseudoacacia. (A) habit
of pycnidia; (B) section through pyenidium; (C) conidia.
DICHOMERA Cooke. Pycnidia black, grouped on stroma, bursting out of bark, globose, ostiolate;
conidiophores simple, conidia dark, globose, ovoid or ellipsoid, several-celled with oblique septa;
saprophytic.
Illustration: D. prunkola; original, from herbarium material on twigs of Prunus virginiana. (A, B) habit
of pycnidia; (C) section of stroma and pycnidia; (D) conidiophores and immature conidia; (E) mature
conidia.
CAMAROSPORIUM Schulz. Pycnidia black, erumpent, globose, separate, ostiolate, papillate;
conidiophores short, simple; conidia dark, ovoid to ellipsoid, with several cross walls and a few
longitudinal or oblique walls; saprophytic on twigs.
Illustration: C. robinae; original, from herbarium material on dead twigs of Robinia pseudoacacia.
(A, B) habit of pycnidia; (C) section of pyenidium; (D) conidiophores and immature conidia; (H) mature
conidia.
CORNULARIA Sacc. Pycnidia dark, stalked, cylindrical, bulbous at the base, or clavatc, usually in tufts
or groups; conidia hyaline to colored, several-celled, fusoid to greatly elongated; parasitic or saprophytic.
Illustration: C. persicae; original, from herbarium material on twig of Prunus. (A, B) pycnidia;
(C) conidia.'
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
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DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
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SPHACELOMA de Bary. Acervuli disc-shaped or cushion-shaped, waxy; conidiophores simple, closely
grouped or compacted, arising from a stromalike base, sometimes almost appearing as a sporodochium;
conidia hyaline, 1-celled, ovoid or oblong; parasitic; imperfect states of Elsinoe; similar to Gloeosporium
and Colletotrichum.
Illustration: S. ampelinmn (Elsinoe ampelina); original, from herbarium material on grape twigs and fruit.
(A) habit on twig; (B) portion of acervulus on twig; (C) portion of acervulus on fruit; (D) conidia.
GLOEOSPORIUM Desm. and Mont. Acervuli subepidermal erumpent, disc-shaped or cushion-shaped,
waxy; conidiophores simple, variable in length; conidia hyaline, 1-celled, ovoid to oblong, sometimes
curved; parasitic, chiefly on leaves or fruits; mostly conidial states of Glomerella.
Illustration: (A-C) G. nervisequum (Gnomonia veneta); (D-F) G. fruiligenum (Glomerella cingulata);
original, from fresh material on Platanus leaves and from culture. (A) habit of fungus; (B) section
through acervulus; (C) conidiophores and conidia; (D) acervuli produced in culture; (E) conidia;
(F) conidiophores and conidia in culture.
COLLETOTRICHUM Corda. Acervuli disc-shaped or cushion-shaped, waxy, subepidermal, typically
with dark, spines or setae at the edge or arr^ong the conidiophores; conidiophores simple, elongate; conidia
hyaline, 1-celled, ovoid or cfofong, to falcate parasitic; imperfect states of Glomerella. This genus differs
'-from Gloeosporium in having spines, which may be absent in some cultures.
Illustration: C. lindemutheanum; original from prepared slide and from culture. (A) section of acervulus
from prepared slide; (B) conidiophores, conidia and setae from culture; (C) conidia; (D) conidia of
C. graminicola.
CATENOPHORA Luttrell. Acervulus cushion-shaped; conidiophores simple, septate, elongate; conidia
hyaline, 1-celled, ellipsoid, produced on lateral sterigmata, one per cell of the conidiophore; parasitic.
Illustration: C. pruni; (A) section through acervulus; (B) conidiophore producing conidia; (C) conidia;
redrawn from Luttrell (271).
PESTALOZZIELLA Sacc. and Ellis. Acervuli subcuticular; conidiophores slender, simple or branched;
conidia hyaline, 1-celled, ovoid or oblong; with a hyaline branched appendage at the apex; parasitic.
Illustration: P. subsessilis; original, from herbarium material on leaves of Geranium caroliniana.
(A) habit on leaf; (B) conidiophores and conidia; (C) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
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DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
MELANCONIUM Link. Acervuli subepidermal or subcortical, conic or discoid, black; conidiophores
simple; conidia dark, I-celled, ovoid to ellipsoid or oblong; parasitic or saprophytic.
Illustration: M. oblongum; original, from herbarium material on dead twigs of Jugulans cinerea.
(A) habit of acervuli; (B) section through acervulus; (C) conidiophores and conidia. Reference (419).
MYCOLEPTODISCUS Ostazeski. Sclerotia small, round, black; acervuluslike fruiting structure;
shieldlike, yellow to brown; stroma a single layer of cells bearing conidia; conidiophores obsolete; conidia
hyaline, 2-celIed, allantoid, with a filamentous appendage at each end (absent in some isolates), parasitic
on legumes.
Illustration: M. (Leptodiscus) lerrestris; (A) spore-bearing upper surface of acervulus; (B) section
through acervulus; (C) conidia; (A) drawn from unpublished photograph furnished by J.W. Gerdemann;
(B, C) drawn from photographs from Gerdemann (145). References (284, 320).
MAKSSONINA Magn. Acervuli subepidermal, discoid, pale; conidiophores short, simple; conidia
hyaline, 2-celled, ovoid to elongate; parasitic, chiefly on leaves.
Illustration: M. populi; original, from herbarium material on leaves of Populus. (A) habit on leaf;
(B) section through acervulus; (C) conidiophores and conidia.
SEPTOGLOEUM Sacc. Acervuli subepidermal, erumpent, pale; conidiophores short, simple; conidia
hyaline, several-celled, oblong to fusoid; parasites on leaves.
Illustration: S. profusum; original, from herbarium material on leaves of Ulmus americana. (A, B) habit
of acervuli; (C) section through acervulus; (D) conidiophores and conidia.
CRYPTOSPORIUM Kunze. Acervuli erumpent, becoming cup-shaped or disc-shaped, stroma brownish;
conidiophores simple or branched; conidia hyaline or subhyaline, l-celled, elongate, falcate; parasitic.
Illustration: C. pinkoia; (A) section through acervuli; (B) conidiophore and conidia; redrawn from
Lindcr (269).
LIBERTELLA Desm. Acervulus subcortical, erumpent, yellow to red; conidiophores branched; conidia
hyaline, l-celled, filiform; saprophytic.
Illustration: L. betulina; original, from herbarium material on bark of Betula lutea. (A) habit of acervuli;
(B) section through acervulus; (C) conidiophores; (D) conidia held together in matrix; (E) separate conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
MELANCONIUM
-\
\
^
\
ft
^
\
MARSSONINA
MYCOUPTODISCUS
SEPTOGLOEUM
CRYPTOSPORIUM
LIBERTELLA
191
192
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
CYLINDROSPORIUM Unger. Acervuli subepidermal, white or pale, discoid or spread out; conidiophores short, simple; conidia hyaline, filiform, straight or curved, l-celled or becoming septate; parasitic
on leaves.
Illustration: C. padi (Coccomyces hiemalis); original, from dried material on cherry leaves. (A, B) habit
of acervuli; (C) section through acervulum; (D) conidiophores and conidia.
MONOCHAET1A Sacc. Acervuli dark, discoid or cushion-shaped, subepidermal; conidiophores slender,
simple; conidia dark, several-celled with hyaline, pointed end cells, elongate to fusoid, with a single apical
appendage; parasitic.
Illustration: M. mali; original, from herbarium material on apple leaf. (A) habit on leaf; (B) section
through acervulus; (C) conidiophores and conidia. Reference (391).
^^
PESTALOT1A de Not. Acervuli dark, discoid or cushion-shaped, subepidermal; conidiophores short,
simple; conidia dark, several-celled, with hyaline, pointed end cells, ellipsoid to fusoid, with two or more
hyaline, apical appendages; parasitic; or saprophytic. References (392, 416).
n
Illustration: P. macrotricha; original, from fresh material on leaves of Rhododendron. (A, B) habit of
acervuli; (C) section through acervuli; (D) conidiophores and conidia; (E) conidia. References (392, 415).
POEYNEMA Lev. Mycelium immersed in substratum, hyaline; acervuli typical with little stromatic
development; conidiophores arising from cells of stroma, conidia single, apical, cylindrical, obclavate,
2-to 3-celled, brown, with single simple or branched apical appendage and 1 to 3 basal appendages.
Illustration: Polynema (Neobarclaya) sp.; redrawn from Sutton (416). (A) section through acervulus;
(B) conidia. Reference (420).
SEIMATOSPORIUM Corda. Acervuli typical, first immersed, erumpent; conidiophores cylindrical,
slender, with a few apical proliferations; conidia borne single and successively on proliferating new
growing points, fusiform to curved, 4- to 6-celled, 2 end cells hyaline, median cells dark, apical appendage
single, simple or rarely branched, basal appendage usually simple; on leaves and twigs. Compare with
Pestahtia.
Illustration: Seimatosporium sp. (Cryptostictis arbuti); redrawn from Sutton (418). (A) portion of
acervulus; (B) developing conidium; (C) conidia.
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
MONOCHAETIA
POLYNEMA
SEIMATOSPORIUM
193
194
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
ENTOMOSPORIUM Lev. Acervulus subcuticular, discoid, dark; conidiophores short, simple; conidia
hyaline, 4-celled, cross-shaped, the two lateral cells smaller, all except the basal cell equipped with a
slender bristle; parasitic on leaves and fruit.
Illustration: E. maculatum (Fabrea maculata); original from herbarium material on leaves of Cydonia.
(A) habit on leaf; (B) section through acervulus; (C) conidia.
CORYNEUM Nees. Acervulus subcutaneous or subcortical, black, cushion-shaped to disc-shaped;
conidiophores slender, simple; conidia dark, several-celled, oblong to fusoid; parasitic or saprophytic.
Illustration: C. kunzei; original, from fresh material on oak twigs. (A) habit of acervuli on twig;
(B) section through acervulus; (C) conidiophores and conidia. Reference (425).
ASTEROSPORIUM Kunze. Acervuli bursting through bark; conidiophores slender, simple; conidia
dark, typically 4-armed, each arm septate, saprophytic.
Illustration: A. hoffmanni; redrawn from Archer (3). (A) section through acervulus; (B) conidia.
PHRAGMOTRICHUM Kunze ex Fries. Fructifications interpreted as acervuli (sometimes pycnidiumlike), stromatic; conidiophores short, upright, simple; conidia yellow or slightly darker, apical in basipetal
chains, phragmosporous or dictyosporous; saprophytic on leaves or twigs.
Illustration: P. karstenii; redrawn from Sutton and Pirozynski (428). (A) acervuluslike fruit structure;
(B) conidiophores and conidia; (C) conidia.
STEGANOSPORlUM Corda. Acei'vuU subcortical, dark, cushion-shaped; conidiophores simple; conidia
dark, dictyosporous, ovoid, oblong or pear-shaped; saprophytic on wood.
Illustration: S. pyriforme; original, from fresh material on bark of Acer. (A) habit of acervuli; (B) section
through acervulus; (C) conidiophores, conidia, and sterile hyphae; (D) conidia. Reference (458).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
-w ^ s ^ ^
CORYNEUM
ENTOMOSPORIUM
ASTEROSPORIUM
STEGANOSPORIUM
PHRAGMOTRICHUM
195
196
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
& ,
'tj?X RHIZOCTONIA DC. Mycelium hyaline in some species to dark in others (such as R. solani), the most
common species; cells of mycelium usually long, septa of branches usually set off from the main hyphae;
asexual fruit bodies and conidia absent; sporodochium-like bodies and chlamydospore-like cells in chains
produced in some species; sclerotia light colored and poorly formed in some species or brown or black
and well formed in other; parasitic, chiefly on roots or other underground parts of plants.
Illustration: R. (Thanatephorus) solarri; original, from culture. (A) small sclerotia and mycelium in tube
culture; (B) section of loose sclerotium; (C) cells of mycelium. References (323, 361).
SCLEROTIUM Tode. Asexual fruit bodies and conidia lacking; sclerotia brown to black, globose or
irregular, compact; mycelium usually light; parasitic, principally on underground parts of plants.
Illustration: S. rolfsii; original, from culture. (A) sclerotia in tube culture; (B) portion of section of
sclerotium; (C) portions of mycelium showing clamp connections.
" *. , (I* . \.u.> v. v> * *-*''
PAP15LOSPORA Preuss. Asexual spores lacking; mycelium light to dark brown, producing compact
clusters of small cells or bulbils which are sclerotium-like and serve to reproduce the fungus; saprophytic,
or parasitic on storage parts of some plants.
Illustration: Papulospora sp.; original, from decaying wood. (A-C) sclerotia produced on mycelium with
clamp connections. References (17, 176, 177).
DESCRIPTIONS AND ILLUSTRATIONS OF GENERA
RHIZOCTONIA
H>
SCLEROTIUM
PAPULOSPORA
197
REFERENCES
1. Ainsworth, G.C.. and G.R. Bisby. 1961. Dictionary of the fungi. Commonwealth Mycological Institute,
Kew, Surrey, England.
2. Amos. R.E., and H.L. Barnett.
1966. Umbehpsis versiforme. a new genus and species of the imperfects.
Mycohgia 58; 805-808.
3. Archer. W.A.
1924.
The morphological development of Asierosporium hoffmanni. Mrcofugia 16:
220-232.
4. Arvao. T, and S. Udagawa.
1974.
Endophragmia dimosphospora, a new hyphomycete. Trans. Mvcol.
Sue. Japan 15: 99-104.
5. Aycrs, XT
1941.
The distribution and association of Gonatorrhodietla highlei with Nectria toccinia in the
United States. Mycohgia 33: 178-187.
6. Baniecki. J.F., and HE Bloss.
1969.
The basidial stage of Phvmatotrichum omnivorum, Mvcologia 6 1 :
1054-1059,
7. Barnett. H.L.
1957.
Hvpuxvlon pumiulaium and its conidia stage on dead oak trees and in culture.
Mycohgia 49: 588-595.
8. Barnett. H.L.
1958.
A new Cakarisporium parasitic on other fungi. Mycohgia 50: 497-500.
9. Barnett. H.L.
1968. The effects of light, pyridoxine. and bioiin on the development of the mycoparasile,
Gonaiobairyuni fuscuni. Mycohgia 60: 244-261.
10. Barnett. H.L.. and F.L. Binder. 1973. The fungal host-parasite relationship. Ann. Rev. Phviopath. 1 1 :
273-292.
1 1 . Barnett. H.L., and V.G. Lilly
1950. Influence of nutrition and environmental factors upon asexual
reproduction of Choaniphora cucurbiiantm. Mycohgia 42: 80-89.
12. Barnett. H.L..and V.G. Lilly
1958.
Parasitism of Catcarisporium parasiticum on species of Physalospora
and related fungi. W. Virginia Univ. Agric. Expt. Sta. Bull. 4207!
13. Barnett. H.L., and V.G. Lilly.
1962. A destructive mycoparasile. Gliocladium roseum. Mycohgia 54:
72-79.
14. Barron, G.L., and L.V. Busch. 1961. Studies on the soil hyphomycete Scolecoba.sidium. Can. J. Bos. 40:
77-84.
15. Barron, G.L. 1962. New species and new records of Oidiodendron. Can. J. Boi. 40: 589-607.
16. Barron. G.L. 1964. A new genus of the hyphomycetes from soil. Mycohgia 56: 514-518.
17. Barron. G.L. 1968. The genera of hyphomycetes from soil. The Williams and Wilkins Co.. Baltimore.
18. Batista. A.C., C.A. Costa, and A . F . Vital. 1957. Novos ou raros Leptostromaceae. Anais Soc. Biol.
Pemamhuco 15; 399-411.
19. Batista. A.C., and R. Cifcrri.
1957. Dictyoarthrinopsis and SerocJachium, two new generaof Moniliaceous
fungi. Alii Inst. Bot. Lab. C r i u . Univ. Pavia 15: 57-62.
20. Bender, H.B. 1931. The genera of Fungi Impcrfecti. North American species and hosts, with particular
reference to Connecticut. Unpublished Thesis. Yale University (reproduced on microcards).
2 1 . Benham, R.W.and J. I.. Miranda. 1953. The genus Beauveria, morphoiogicaland taxonomicat studies of
several species and two strains isolated from wharfpiling borers. Mycohgia 45: 727-746.
22. Benjamin. R.K. 1958, Sexuality in the Kickxelliaceae. Aliso 4: 149-169.
23. Benjamin. R.K, 1959, The merosporangiferous Mucorales. Aliso 4: 321-433.
24. Benjamin. R.K. I960. Two new members of the Mucorales. Aliso 4: 523-530.
25. Benjamin, R.K. 1963. Addenda to "The merosporangiferous Mucorales." Aliso 5: 273-288.
26. Benjamin, R.K.
1966. The merosporangium. Mycohgia 58: 1-42.
27. Bessey. E.A.
1907. Spore forms of Spega::inia ornata. Jour. Mycol. 13: 43-45.
. 28. Bessey. E.A. 1950. Morphology and taxonomy of fungi. The Blakiston Co., Philadelphia.
198
REFERENCES
199
29. Bessey, E.A. 1953. Notes on the genus Camptomeris. Fungi Imperfecti. Mycologia 45: 364-390.
30. Beverwijk, A.L. 1953. Helicosporous hyphomycetes I. Trans. Brit- Mycol. Soc. 36: 111-124.
3 1 . Bhatt, G.C,and W.B. Kendrick.
1968. The general concepts of Diphrhinotrkhunr and Daciylaria and a
new species of Daciylaria from soil. Can. J. Boi. 46: 1253-1257.
32. Binder, F.L., and V.G. Lilly. 1976. Qualitative and quantitative effects of radiation on pycnidial formation
by Dendraphoma obscurans. Can. J. Sot. 54: 566-571.
33. Bisby, G.R 1943. Siachybotrys. Wans. Brit. Mycol. Soc: 26: 133-143.
34. Bisby. G.R. 1945. Siachybotrys and Memnoniella. Trans. Brit. Mvcol. Soc 28: 11-12.
35. Bisby, G.R. 1952. The name Oidium. Trans. Brit. Mycof. Soc 35: 236-237.
36. Boedijn, K.B. 1927. Uber Rapalomyces e/egans Corda. Ann. Mycol. 25: 1 6 1 - 1 6 6 .
37. Boedijn. K.B. 1950. Notes on the genus Cylindrocladium. Reinwardtia I: 51-60. (Published by the
Herbarium Bogoriense. Kebun Raya, Indonesia.)
38 Booth. C. 1966. The genus Cylindroiarpon. Mycol. Papers C.M.I. 104: 1-56.
39. Booth, C, and J.S. Murray. I960. Caloneciriahederae and its Cylindrocladium conidial state. Trans. Brit.
Mycol. Sot: 43: 69-72.
40. Brooks, F.F., and C.G. Hansford. 1922. Mould growth upon cold-store meat. Trans. Brit. Mvcol. Soc
8: 113-142.
4 1 . Brown, A.H.S.. and G. Smith. 1 9 5 7 . The genus Paeiilomyces Bainierand its perfect stage Byssochlamys
Westling. Trans. Brit. Mycol. Soc. 40: 17-89.
42. Brown. J.C., and W.B. Kendrick. 1958. Gliomastix gutiuliformis sp. nov. Trans. Brit. Mvcol. Soc
41:499-500.
43. Brown, M.F., and H.G. Brotzman. 1979. Phytopathogenic Fungi. A Scanning Electron Stereoscope
Survey. University of Missouri, Columbia Extension Division. Columbia, Mo.
44. Buckley, P.M.. T.D. Wyllie, and J.E. DeVay. 1969. Fine structure of comdia and conidium formation in
Verticillitim alboatrum and V. migrescens. Mycologia 6 1 : 240-250.
45. Buller, A.H.R. 1933. Sporobolomvces, a basidiomycetous genus: in Researches on Fungi. Vol. 5. pp.
171-206. Longmans, Green and Company, London.
46. Butler, E.E.. and A . H . McCain. 1968. A new species of Stephanotna. Mycologia 60: 955-959.
47. Cain. R.F. 1952. Studies or Fungi Imperfecti I, Phialophora. Can. J. Hot. 30: 338-343.
48. Calderone, R.A., and H.L. Barnett. 1972. Axenic growth and nutrition of Gonaiobotryum fuscum.
Mycologia 64: 153-160.
49. Caldwell, R.M. 1 9 3 7 . Rhvnehosporium scald of barley, rye. and other grasses. Jour. Agr. Res. 55: 175-198.
50. Carmichael, J.W. 1 9 5 7 . Geotrichum candidum. Mycologia 49: 820-830.
5 1 . Carmichael, J.W. 1962. Chrysosporium and some other aleuriosporic hyphomycetes. Can. J. Bot. 40:
1137-1173.
52. Cejp, K., and F.C. Peighton. 1 9 6 9 . Microfungi 1 1 1 . Some African s p e c i e s of Pliyllosucta and Septoria;
new genera and species redisposition of some hyphomycetes. Mycol. Papers C.M.I. 117: 1-31.
53. Chcsters, C.G.C., and G.N. Greenhaigh. (964. Geniculosporium serpens gen. el sp. nov.. the imperfect
state of Hypoxylon serpens. Trans. Brit. Mycol. Sot. 47: 393-401.
54. Chona, B.L.. R.L. Manjal, and B.S. Bajaj. 1956. Vasudevella. a new genus of the Sphaeropsidales. Indian
Phytopath. 9: 186-190.
55. Chupp, C. 1954. A monograph of the Genus Cercospora. Cornell University Press, Ithaca, New York.
56. Clements. FE..and C.L. Shear. 1931. The Genera of Fungi. H.W. Wilson Co.. New York.
57. Cole, G.T., and W.B. Kendrick. 1968. Conidium ontogeny in hyphomycetes. The imperfect state of
Monascus ruber and its meristem arthrospores. Can. J. Bot. 46: 987-992.
58. Cole, G.T, and B. Kendrick. 1970. Conidium ontogeny in hyphomycetes. Development and morphoiogy
of Cladobotryum. Can. J. Bot. 49: 595-599.
59. Conant, N.F., D.S. Martin. D.T. Smith. R.D. Baker.and J.L. Callaway. Manual oj clinical mycology. W B.
Saunders Company. Philadelphia.
60. Cooke, R.C.andC.H. Dickinson. 1965. Nematode-trapping species of Dactvlella and Monairosporium.
Trans. Brit. Mycol. Soc 48: 621-629.
6 1 . Cooke. R.C.and B.E.S. Godfrey. 1964, A key to the nemaiode-destroying fungi. Trans. Brit. Mvcol. Soi:
47: 61*74.
62. Cooke, W.B. 1954. The genus Arthriniunt. Mycologia 46: 815-822.
200
REFERENCES
63. Cooke, W.B.
1959.
An ecological life history of Aureobasiclium pullulans (de Bary) A r n a u d .
Mycopaihologia 12: 1-45.
64. Coonty, D.G., and R. Emerson. 1964. Tiiermophyilic Fungi. W.H. Freeman and Co., San Francisco.
65. Crane. J.L., and J.I). Schofcnecht.
1973.
Conidiogencsis in Ceratocysiis tilmi. Ceratocysiis piceat; and
Graphium penicillioules. Aiiier. J. Boi. 60: 346-354.
66. Cunnel, G.J. 1956. Some pyenidial fungi on Carex. Trans. Urn. Mycol. Soc 39: 21-47.
67. Cunnell, G J .
1957. On Neoitiospora caricina (Desm.) Hohnel. Trans. Brii. Mycol, Soc. 40: 438-442.
68. Cunnell. O.J,
1957. Stagartospora spp. on Pnragmiies communis. Trans. Bril. Mycol. Soc 40: 443-455.
69. Cunnell. G.J.
1958. On Robillardaphragmites sp. nov. Trans. Brit. Mycol. Sot: 4 1 : 405-412.
70. Cutter, V . M .
1946. The genus Cuniminghamclla (Mucorales). Farlowia 2: 321-343,
7 1 . Damon, S.C.
1950.
A laxonomic consideration of two cheirosporous genera, Chieromvies and Pedilospora. Mycohgia 42: 554-562.
72. Damon, S.C.
1952. Two noteworthy species of Sepedonium. Mycohgia 44: 86-96.
73. Damon, S.C.
1952. Type studies in Dicivosporium, Spieria. and Caitanea. Uoydia 15: 110-124.
74. Damon, S.C.
1953. Notes on the hyphomycetous genera Spegazzinia and Isthmospora Stevens. Bull.
Torrey. Bot. Club 80: 155-165.
75. Daniels, J.
1961.
Chaetomium piluli/erum sp. nov., the perfect state of Boiryotrichum piluliferum. Trans.
Bril. Mycol. Soc. 44; 79-86.
76. Davidson. R.W.
1950,
Urnula craterium is possibly the perfect stage of Srrumella corvneoidea. Mvcologia
42: 735-742.
77. Davidson, R.W. [955. Wood-staining fungi associated with dark beetles in Englemann spruce in
Colorado. Myculogia 47: 58-67.
78. Deighion, F.C,
1967. Studies on Cercospora and allied genera It. Passalora. Cercosporhliutn, and some
species of Fusicladium on Euphorbia. Mycol. Papers C . M . I . 112: 1-80.
79. Deighion. F.C. 1968. Spermospora. Trans. Brii. Mvcot. Soc. 5 1 ; 41-49.
80. Deighton, F.C. 1969. Microclavia. Trans. Bril. Mycol. Soc. 52; 315-321.
8 1 . Deighton, F.C. 1973, Studies on Cercospora and allied genera IV. Cercosporella Sacc, Pseudocercosporella gen. nov.. and Pseudocercosporidium gen. nov. Mycol. Papers C . M . I . 133.
82. Deighton, F.C.
1973. Five North American Cenospora-likt fungi. Tram. Brit. Mycol. Soc. 61: 107-120.
83. Deighton. F.C.
1976. Studies on Cercospora and allied genera V I . Pseudocercospora Speg., Pantospora
at.,nn<lCercosepioria Petr. Mycol. Papers C . M . I . 140: 1-168.
84. Deighton, F.C. 1979. Studies on Cercospora and allied genera V I I . New species and redispositions.
Mycol Papers C.M.I. 144; 1-56.
85. Deighton. F.C. and K.A. Pirozynski.
1969.
Microfungi I I . Bwoksia and Grallomyces: Acrogenoiheca
ornaia sp. nov.; the genus Xenosporium. Mycol. Papers C . M . I , 105; 1-35.
86. DeLamater. E. D.
1948.
The nuclear cytology of Blastomyces dermatiiidis. Mycohgia 40: 430-444.
87. Deseals, E,. and J. Webster.
1980. Taxonomic studies on aquatic hymenomycetes J], The Vendrospora
aggregate, Trans, Brii. Mycol. Soc 74: 135-158.
88. Deseals, I: , and J. Webster. 1982. Taxonomic studies on aquatic hyphomyectes 111. Some new species and
a new combination. Trans, Brii. Mycol. Soc 78: 405-437.
89. Deseals, ¥... and J. Webster. 1983. laxonomic studies on aquatic hyphomycetes IV. Pure culture and
typification of various species. Trans. Bril. Mycol. Soc 79: 45-65.
90. DeVries, G.A.
1952.
Contribution to the knowledge of the genus Cladosporium. Centraalbureau voor
Schimmelculturcs. Baarn.
9 1 . Dickinson, C . H , 1964. The genus Wardonmes. Trans. Brii. Mvcot. Soc. 47: 321-325.
92. Dickinson. C . H . 1968. Gliomaslix Gueguen. Mycol, Papers C M . I . 115: 1-24.
93. DiCosmo. F.S., S. Berch. and B. Kendrick.
1983. Cylindrotriclnini. Chaeiopsis and two new genera of
hyphomycetes, Kylindria and Xenokvlindria. Mycohgia 75: 949-973.
94. Dichl, W.W.
1950. Balansia and Btilansiae in America, Agriculture Monograph No. 4, U.S.D.A.,
Washington, D.C
95. Downing. M . H .
1953.
Boirvoirichum and Coccospora. Mycohgia 45: 934-940,
96. Drechsler. C.
1923. Some graminicolous species of Hetmimhosporium. Jour. Agr. Res. 24: 641-740.
97. Drechsler, C
1934.
Pedilospora dacivhpaga n. sp., a fungus capturing and consuming testaceous
rhi/opods. Wash. Acad, Sci. 24: 395-402,"
98. Drechsler, C.
1934.
A new species of Helkocephalum. Mycohgia 26: 33-37,
REFERENCES
201
99. Drechsler. C.
1937. Some hyphomycetes that prey on free-living terricolous nematodes. Mvcologta 29:
446-552.
100. Drechsler, C.
1937. A species of Tridentaria preying on Diffieugia conslricia. Wash. Acad. Sci. 27:
391-398.
1940. Three new hyphomycetes preying on free-living terricolous nematodes. Mvcologta
101. Drechsler, C.
32: 448-470.
102. Drechsler, C.
1941. Some hyphomycetes parasitic on free-living terricolous nematodes. Phytopathology
3 1 : 773-802,
1946. A clamp-bearing fungus parasitic and predaceous on nematodes. Mycologia 38: 1-23.
103. Drechsler. C.
1950. Several species of Oactylella and Dactylaria that capture free-living nematodes.
104. Drechsler, C.
Mycologia 42: 1-79.
105. Drechsler, C. 1957. A nemalode-capturing Phycomycete forming ch la mydos pores terminally on lateral
branches. Mycologia 49: 387-391.
1957. The Friendly Fungi. Farberand Farber, London.
106. Duddington, C.L.
107. DuPlessis, S.J., and J.A. Truter. 1953. Brown spot disease of lupines caused by Pleiovhaeta setosa
(Kichn.) Hughes. Union of South Africa Dept. Agr. Sci. Bull. 347.
1963. Notes on Cephalosporin™ species. Colorado State University Bulletin.
108. Durrell, L.W.
109. Edward, J.C. 1959. A new genus of Moniliaceae. Mycologia 5 1 : 781-786.
110. Elliott, E.S.
1949. The effects of sugar concentration on conidial size of some species of Helminlhosporium. Phytopathology 39: 953-958.
111. Ellis, J.J., and C.W. Hesseltine. 1962. A new genus of Moniliales having penicilli subtended by sterile
arms. Bull. Torrev Bot. Club 89: 21-27.
112. Ellis. M.B. 1949. Tetraploa. Trans. Brit. Mycol. Sot: 32: 246-251.
113. Ellis. M.B. [958. Clasterosporium and some allied genera—Phragmospurae I. Mycol. Papers C . M . I ,
70: 1-89.
114. Ellis, M.B. Clasterosporium and some allied genera- Phragmusporae I I . Mycol. Papers C . M . I . 72: 1-75.
115. Ellis, M.B. 1960. Dematiaceous hyphomycetes 1. Mycol. Papers C . M . I , 76: 1-36.
116. Ellis. M.B. 1961. Dematiaceous hyphomycetes I I . Mycol. Papers C . M . I . 79: 1-23.
117. Ellis. M.B. 1961. Dematiaceous hyphomycetes Ml. Mycol, Papers C . M . I . 82: 1-55.
118. Ellis. M.B. 1963. Dematiaceous hyphomycetes (V Mycol, Papers C.M.I. 87: J-42.
119. Ellis, M.B. 1963. Dematiaceous hyphomycetes V. Mycol. Papers C . M . I . 93: 1-33.
120. Ellis, M.B. 1965. Dematiaceous hyphomycetes V I . Mycol. Papers C . M . I . 103: 1-46.
Dematiaceous hyphomycetes V I I . Curvularia. Brachosporium. etc. Mycol. Papers
121. Ellis, M.B.
1966,
C . M . I . 106; 1-57.
122. Ellis, M.B. 1967. Dematiaceous hyphomycetes V I I I . Periconiella, Trichodochium, etc, Mycol. Papers
C . M . I . I l l : 1-46.
123. Ellis, M.B.
1968. Dematiaceous hyphomycetes IX. Spiropes and Pleuruphragmium. Mycol. Papers
C . M . I . 114: 1-44.
124. Ellis. M.B. 1971. Dematiaceous hyphomycetes. Commonwealth Mycologica! Institute. Kcw, Surrey.
England.
125. Ellis, M.B., E.A, Ellis, and J.R Ellis. 1951. British marsh and fen fungi I. Trans. Brit. Mycol. Sot:
34: 147-169.
126. Ellis, M.B,. E.A. Ellis, and J.R Ellis. 1951. British marsh and fen fungi I I . Trans. Brit. Mvcol. Sot:
34:497-514,
127. Embrcc, R.W. 1959. Radiomvees, a new genus in the Mucorales. Am. J. Bot. 46: 25-30.
128. Embree, R.W. 1963. The status of Gliocephalis. Mvcologta 55: 127-128,
129. Emmons. C.W.. C H . Binford. and J.R Utz.
1963. Medical Mycology Lea and Febigcr, Philadelphia.
130. Engler, A., and K. Prantl. 1900. Die naturlichen Pflanzcnfamilien. I. Abteilung I. Wilhelm Engelmann,
Leipzig.
1910. An important entomogenous fungus. Mycologia 2: 164-168.
131. Fawcett. H.W.
1932.
Mycotypha iniaospora, a new genus of Muroraccae. Mycologia 24: 187-198.
132. Fcnner, E.A.
}33. Fergus, C.L.
(957.
Myrotheciunt rorkhim on gardenia. Mycologia 49: l24-!27.
134. Fergus, C.L. 1960. A note on the occurrence of Peiziza ostracoderma. Mycologia 52; 959-961.
1950. Two new species of Hirsutella Patouillard, Mycologia 42: 290-297.
135. Fisher. F.E.
1930.
The Lower Fungi. McGraw-Hill Book Co., New York.
136. Fit/patrick, H.M,
137. Friend. R.J. 1965. What is Fumago vagans.' Trans. Brit. Mycol. Sot: 48: 371-375,
202
1.18.
139.
140.
141.
142.
143.
144.
145.
146.
147.
148.
149.
150.
151.
152.
153.
154.
155.
REFERENCES
G a i n , R . L . a n d H.L. Barnett.
1970.
Parasitism and axenic g r o w t h of the mycoparasite, Gonaiorrhodiella
highlei. Mycohgia 62: [122-1129.
Gams, W.
1975.
Cephahsporium-\ike hyphomycetes: Some tropical species. Trans. Brit. Mvcol. Sue.
64: 389-404.
G a m s . W.. and W.R. M c G i n n i s .
198.1.
Phialemonium, a new a n a m o r p h genus intermediate between
Phialophora and Acremonium.
Mycohgia 75: 977-987.
Garraway, M O . , and R.C. Evans.
1984.
fungal Nutrition and Physiology John Wiley and Sons, New
York.
G e o r g , L.K.
1951.
The relation of n u t r i t i o n to the g r o w t h and m o r p h o l o g y of Trichophyton violaceum I I .
The influence of n u t r i t i o n a l factors on the morphology of T. violaceum. Mycohgia 43: 536-548,
G e o r g . L.K.
1956.
Studies on Trichophyton tonsurans 1. The t a x o n o m y of T. tonsurans. Mvcologia
4 8 : 65-82.
G e o r g . L..K.
1956.
Studies on Trichophyton tonsurans I I . M o r p h o l o g y and laboratory i d e n t i f i c a t i o n .
Mycohgia 48: 354-370.
G e r d e m a n n , J.W.
1953.
An undescribed fungus causing a root rot of red clover and other Leguminosae.
Mycohgia 45: 548-554.
G l e n - B o t t , J . l . 1951. Helocodendron giganieum n. sp. and other aerial-s p o r i n g hyphomycetes of
submerged dead leaves. Trans. Brit. Mycol. Soc. 3 4 : 275-279.
Glen-Bott, J . l .
On Helkodendron tubulosum and some similar species. Trans. Brit. Mycol. Soc. 38: 17-30.
G o i d a n i c h , D.G.
1933.
Intorns ad alcuni micromiceti nuovi o r a r i . Ann. Mycol. 3 1 : 134-143.
G o i d a n i c h . G.
1935.
Una nova specie di Ophiostoma viviente sul pero ed aicune osservazioni sulf esatta
posi?ione sistematica della forma ascofora e delle forme metagenotiche del gencre. Bull della R. Stazione di
Pathologia vegetale di R o m a . N.S. 13.
G o i d a n i c h , G.
1946.
Peyronellaea nuovo genere di deuteromiceti Rendicont: d e l l ' Academia Nazionale
dci Lincci. Scr. 8 . 1 : 449-457.
Goos, R.D.
1969.
C o n i d i u m ontogeny in Cacumisporium capitalatum. Mycohgia 6 1 : 52-56.
Goos. R.D.
1969.
The genus Pleurothecium. Mycohgia 6\: 1048-1053,
Goos, R.D., and E.F. M o r r i s .
1965.
Murogenella terricola, a new dematiaceous fungus f r o m s o i l .
Mycohgia 57: 776-781.
G r e e n h a l g h , G . N . . and C.G.C. Chesters.
1968.
C o n i d i o p h o r e m o r p h o l o g y in some British members of the
Xylariaceae. Trans. Brit. Mycol. Sot. 5 1 : 57-82.
Gregory, P H . , and M.E. Lacey.
1964,
The discovery of Pithomvces chartarum in Britain. Trans. Brit.
Mycol. Soc. 47: 25-30.
156. Gregory. P H . . and S. Waller.
1951.
Crypiostroma corticate and sooty bark disease of sycamore (Acer
pseudoplatanus). Trans. Brit. Mycol. Soc. 34: 578-597.
157. G r i f f i n , D . H .
1981.
Fungal Physiology John Wiley & Sons, New York.
158. Groves. J . W , and A . J . S k o l k o .
1946.
Notes on seed-borne fungi IV. Acremoniel/a, Chlamvdomyces, and
TrichoclaJium. Can. J. Res. C. 24: 74-80.
159. H a a r d , K.
1968.
Taxonomic studies on the genus Anhrobotrvs C o r d a . Mycohgia 60: 1140-1159.
160. Harter, L.L.
1916.
Sweet potato scurf. Jour. Agr. Res. 5: 787-792,
1 6 1 . Haskins, R . H . . and J.F.T Spencer.
1967.
Trichosporonoides oedocephalis n. g e n . , n. sp. I. M o r p h o l o g y ,
development and taxonomic position. Can. J. Bot. 45: 515-520.
162. Hawker. L.L.
1950,
Physiology of Fungi. University of L o n d o n Press. L o n d o n .
163. H e a l d , F.D.
1909.
A species of Discosia on living bull pine seedlings. Mycohgia 1: 215-217.
164. Hennebert, G.L.
1962,
Wardomyces and Asteromyces. Can. J. Bot. 4 0 : 1203-1216,
165. Hennebert, G.L.
1968,
New species of Spirosphaera. Trans. Brit. Mycol. Soc. 5 1 : 13-24.
166. Hennebert, G . L .
1968.
Fchinobotryum.
Wardomyces. and Mammaria.
Trans.
Brit. Mycol. Soc.
51:749-762,
. '
167. Hennebert. G.L.
1973.
Botrytis and Botrytis-Yike genera. Persoonia 7: 183-204.
168. Hennebert, G.L., and R.P, K o r f .
1975.
The peat m o l d , Cromelosporium ollare, conidial state of Peziza
osirachoderma and its misapplied names, Botrytis crystallina, Botrytis spectabilis. Ostrochoderma epigaeum,
and Peziza aruninoaa. Mycohgia 67: 214-240.
169. Henry, B.H,
1944.
Chalara uuenina n. sp.. the cause of oak wilt. Phytopathology 34: 631-635.
170. Hesseltine, C.W.
1943.
Haphsporangium bisporale. Mycohgia 35: 255-256.
1 7 1 . Hesseltine, C.W.
1952.
A survey of the Mucoralcs. Trans. N.Y. Acad. Set. Ser. 2. 14:210-214.
-,
REFERENCES
203
172. Hesseltine. C.W.. and C.R. Benjamin. 1957. Notes on the Choanephoraceac. Mycologia 49: 725-733.
173. Holubova-Jechova, V. 1973. Legnicolotis hyphomycetes from Czechoslovakia 3. Sporoschisma,
Sporoschismopsis. and Calanularia. Folia Geoboi. Phyioiax. S: 209-218,
174. Holubova-Jechova, V. 1973. Lignicolous hyphomycetes from Czechoslovakia 4. Menixpora. Folia Geobot.
Phyioiax. 8:317-336.
175. Holubova-Jechova, V. 1978. Ligmcalous hyphomycetes from Czechoslovakia 5. Sepionema, Honviacielta,
and Lylea. Folia Geoboi. Phyioiax. 13: 421-442.
176. Hoison. H.H. 1971. Notes on bulbiferous fungi, with a key to described species. Bui. Go:. 64: 265-284.
177. Hotson, H.H, 1942. Some species of Papuhispora associated with rots of Gladiolus bulbs. Mycologia 34:
391-398.
178. Howell, A. 1939. Studies on Histoplasma capsulaium and similar form species I. Morphology and
development. Mycologia 31: 191-216.
179. Hubert, E.E.
1935.
Observations on fubercuiina maxima, a parasite of Cronanium ribicola.
Phytophatology 25: 253-261.
180. Hudson, H J . 1963. The perfect state of Nigrospora oryzae. Tram. Bril. Mycol. Soc. 46: 355-360.
181. Hudson, HJ., and B.C. Sutton. 1964, Triscelosporium and Teiranacrium. two new genera of Fungi
Imperfecti. Trans. Bril. Mycol. Soc. 47: 197-303.
182. Hughes, S.J. 1949, Studies in micro-fungi 1. The genus Fisariella Sacc, Mycol. Papers C.M.I. 28.
183. Hughes, S.J. 1949, Studies in micro-fungi II- The genus Sporoschisma Berkeley and Broome and a
redescription of Hehninthosporium rousselianutn Montagne. Mycol, Papers C.M.I. 31: 1-33.
184. Hughes, S J . 1951. Studies on micro-fungi 111- Mastigosporium, Camposporium, and Ceraiophorum.
Mycol. Papers C.M.I. 36: 1-43,
185. Hughes, S J . 1 9 5 1 . Studies on micro-fungi V. Acrotheca. Mycol. Papers C.M.I. 38: 1 - 8 .
186. Hughes. SJ. 1951. Studies on micro-fungi VI. Ceralosporium, Hirundinaria. and Hipperocrepidium.
Mycol. Papers C.M.I. 39: 1-24.
187. Hughes. S J . 1951. Studies on micro-fungi IX. Calcarisporium, Verticicladium, and Hansfordia (gen.
nov.). Mycol. Papers C.M.I. 43: 1-24.
188. Hughes, S J . 1951. Studies on micro-fungi X- Zygosporium. Mycol. Papers C.M.I. 44: 1 - 1 8 .
189. Hughes, S J . 1951. Some hyphomycetes which produce phialides. Mycol. Papers C.M.I. 45: 1-36.
190. Hughes, S.J. 1951. Studies on micro-fungi XII. Triposporium, Tripospermum, Ceraiosporella, and
Tetrasporium (gen. nov.). Mycol. Papers C.M-I. 46: 1-35.
191. Hughes, S.J. 1951. Studies on micro-fungi XII]. Belirania, Ceraiocladium, Diplorhlnoirichuni, and
Hamfurdtella (gen. nov.), Mycol. Papcts C.M.I. 47: 1-15.
192. Hughes. SJ. 1951. Anneliophora nom. nov. (Chaetotrichum Syd. nan Rabenh.). Trans. Bril. Mvcol. Soc.
34: 544-550,
193. Hughes, S J . 1951. Stachvlidium, Gonvtrichutn, Mesobotrvs. Chaeiopsis, and Chaeiopsel/a. Trans. Bril.
Mycol. Soc. 34:551-576.
194. Hughes, SJ. 1951. Brachyspurium in Britain. The Naiuralisi, April-June, pp. 45-48.
195. Hughes, S J . 1951. Arthrobotryum Cesati, The Naiuralisi. October-December, pp. 171-172.
196. Hughes. S J . 1951, Septomena secedens Corda. T)w Naiuralisi. October-December, pp. 173-176.
197. Hughes. S J . 1951. Sclerographiwn aierriinum Berkeley. Indian Phviopaih. 4: 5-6,
198. Hughes. S.J. 1951. Fungi from the Gold Coast I. Mycol. Papers C.M.I. 48.
199. Hughes, S J . Studies on micro-fungi XIV Stigmella, Stigmina, Camptomeris, Polyihrincium, and
Fusicladietla. Mycol. Papers C.M.I. 49: 1-25.
200. Hughes, S J . 1952. Tnchocladium Har/. Trans. Brit. Mvcol. Soc. 35: 152-157.
201. Hughes, SJ. 1952. Speira stipitata. Trans. Bril. Mycol. Soc. 35: 243-247.
202. Hughes, SJ. 1952. Four species of Septoriema. The Naturalist. January-March, pp. 7-12.
203. Hughes. SJ. 1952. Daciylospohum in Britain. The Naiuralisi. April-June. pp. 63-64.
204. Hughes. SJ. 1952. Sirodesmium granuhsum and Torula diversa. Tiie Naiuralisi. July-September, pp.
93-98.
205. Hughes, S.J. 1953. Some foliicolous hyphomycetes. Can. J. Bot. 31: 560-576.
206. Hughes, S.J. 1953. Conidiophores. conidia and classification. Can. J. Bot. 31: 577-659.
207. Hughes. S J . 1953. Fungi from the Gold Coast II. Mycol, Papers C.M.I. 50: 1 - 1 0 4 .
208. Hughes. S J . 1953. Podoconis in Britain. 7 7 I E > Naturalist. July-September, pp. 119-124.
209. Hughes. S.J. 1955. Micro-fungi I, Cordana, Brachysporium, Phragmocephala. Can. J. Bot. 33: 259-268.
j$4
REFERENCES
210. Hughes, S J . 1958. Revisiones hyphomycetum aloquot cum appendice de nomimibus rejiciendis. Can. J.
Bot. 36: 727-836.
211. Hughes, S.J. 1959. Micro-fungi IV. Trkhocladium canadense n. sp. Can. J. Bot. 37: 857-859.
212. Hughes, S.J. 1959. Starting point of nomenclature of hyphomycetes. Thxon. 8: 96-103.
213. Hughes, S.J., Ed, Fungi canadensis. National Mycological Herbarium, Ottawa, Ontario. (Published at
intervals with illustrations.)
214. Hughes, S.J..and G.L. Hennebert. 1961. Microfungi VIII. Balanium Wallroth. Can. J. Bot. 39: 1505-1508.
215. Hughes, S.J., and WB. Kendrick. 1963. Microfungi IX. Menispora Persoon. Can. J. Bot. 41: 693-718.
216. Hulbray, R.L. 1941. A needle blight of Austnan pine. Bull. III. Nat. Hist. Surv. 21: 231-236.
217. Hunter, B.B.. and H.L. Barnett. 1973. Deuteromycetes (Fungi lmperfecti) in Handbook of Microbiology.
H.L. Lechevalier, ed. Vol. I. Organismic Microbiology. CRC Press, Cleveland.
218. Hunter, B.B., H.L. Barnett, and T.R Buckelaw. 1978. Deuteromycetes (Fungi lmperfecti) in Handbook of
Microbiology. 2nd ed. Vol. II. Fungi, Algae. Protozoa, and Viruses. L.S. Laskow and H.L. Lechevalier, ed.
CRC Press.
219. Hunter, B.B., J.V. Hoyes, and H.L. Barnett. 1974. The addition of aureomycin and chloramphenicol to
various fungal media to prevent bacterial contamination. Proc. Pa. Acad. Sci. 48: 88-92.
220. Hwang, K., D.A. Stelzig, H.L. Barnett, RR Roller, and M.I. Kelsey. 1985. Partial purification of the
growth factor, mycotrophein. Mycologia 77: 109-113.
221. lchinoe, M. 1968. Japanese hyphomycete notes II. Trans. Mycol. Soc. Japan 9: 57-64.
222. lchinoe, M., and H. Kume. 1970. Japanese hyphomycete notes IV. Some helicosporous hyphomycetes in
Japan. Trans. Mycol. Soc. Japan II: 98-108.
223. Ingold, C.T. 1942. Aquatic hyphomycetes of decaying alder leaves. Trans. Brii. Mycol. Soc. 25: 339-417.
224. Ingold, C.T. 1943. Triscelophorus monosporus n. gen., n. sp., an aquatic hyphomycete. Trans. Brit. Mycol.
Soc. 26: 148-152.
225. Ingold, C.T. 1944. Some new aquatic hyphomycetes. TYans. Brit. Mycol. Soc. 27: 35-47.
226. Ingold, C.T. 1952. Actinospora megalospora n. sp., an aquatic hyphomycete. Trans. Brit. Mycol. Soc.
35: 66-70.
227. Ingold. C.T. 1956. The conidial apparatus of Trichothecium roseum. Tram. Brit. Mycol. Soc. 39:460^64,
228. Ingold, C.T. 1958. New aquatic hyphomycetes: Lemonniera brachycladia. Anguillospora crassa, and
Fluminispora ovaiis. Trans. Brit. Mycol. Soc. 41: 365-372.
229. Ingold, C.T. 1958. Fluminispora ovaiis Ingold antedated by Dimorphosporafoliicola Tubaki. Trans. Brit.
Mycol. Soc. 41:412.
230. Ingold, C.T 1960. Aquatic hyphomycetes from Canada. Can. J. Boi. 38: 803-806.
231. Ingold, C.T 1964. A new species of Ingoldia from Britain. Trans. Brit. Mycol. Soc. 47: 103-107.
232. Ingold, C.T. 1975. An illustrated guide to aquatic and water borne hyphomycetes (Fungi lmperfecti) with
notes on their biology. Freshwater Biol. Assoc. Sci. Publ. 30. Ferry House.
233. Ingold, C.T, and V.J. Cox. 1957. On Tripospermum and Campyhspora. Trans. Brit. Mycol. Soc.
40: 317-321.
234. Ingold, C.T, V. Dann, and PJ. McDougall. 1968. Tripospermum camelopardus sp. nov. Trans. Brit.
Mycol. Soc. 51:51-56.
235. Iqbal, S. H. 1971. New aquatic hyphomycetes. Trans. Brit. Mycol. Soc. 56: 343-352.
236. Isaac, I. 1953, A further comparative study of pathogenic isolates of FmjW///«m.' V.nubilum Pethybr. and
V. iricorpus sp. nov. Tram. Brit. Mycol. Soc. 36: 180-195.
237. Isaac, I. 1955. A new hyaline species of Verticillium: V. intertextum sp. nov. Trans. Brit. Mycol. Soc.
38: 143-156.
238. Jacques, J.E. 1941. Studies in the genus Hetersporium. Contrib. Inst. Bot. Univ. Montreal No. 39.
239. Jackson, C.R., and G.F. Weber. 1959. Morphology and taxonomy of Ahernaria cucumerina. Mycologia
51:401-408.
240. Jackson, H.S., and E.R. Dearden. 1948. Martensella corticii Thaxter and its distribution. Mycologia
40: 168-176.
241. Jones. F.R. 1918. Yellow leaf blotch of alfalfa caused by the fungus Pyrenopeziza medicaginis. J. Agr. Res.
[3: 307-329.
242. Jong, S.C., and J.D. Rogers. 1968. The conidial state of Hypoxolon microplacum. Mycologia 60:
793-796.
REFERENCES
205
243. Jong, S.C., and J.D. Rogers. 1972. Illustrations and descriptions of conidial states of some Hypoxolon
species. Wash. Agric. Expl. Sta. Tech. Bull. 71.
244. Karling, J.S. 1935. Tetracladium marchalianum and its relation to Asterothrix, Phycastrum and
Cerasterias. Mycologia 27: 478-495.
245. Karling, J.S. 1938. Harposporium anguillulae. Mycologia 30; 512-519.
246. Kelman. R, 1967. Sourcebook of laboratory Exercises in Plant Pathology. Sourcebook Committee of
American Phytopathological Society. W.H. Freeman and Co., San Francisco.
247. Kendrick, W.B. 1958. Sympodielta. a new hyphomycete. Trans. Brit. Mycol. Soc. 41: 519-521.
248. Kendrick, W.B. 1961. Hyphomycetes of conifer leaf litter. Thysanophora gen. nov. Can. J. Bol. 39:
817-832.
249. Kendrick. W.B. 1961. The Leptographium complex. Phiahcephala gen. nov. Can. J. Bot. 39: 1079-1085.
250. Kendrick, W.B. 1961. The leptographium complex. Vertieicladiella Hughes. Can. J. Bot. 40: 771-797.
251. Kendrick, B., ed 1971 Taxonomy of Fungi Imperfecti'. University of Toronto Press, Toronto.
252. Kendrick, W.B., and J.W Carmichael. 1973. Hyphomycetes, p. 323-509, in The Fungi IV. Academic
Press, New York.
253. Kendrick, W.B., and G.T. Cole. 1968. Conidium ontogeny in hyphomycetes. The sympodulae of
Beauvaria and Curvularia. Can. J. Bot. 46: 1297-1301.
254. Kendrick, W.B., and G.T. Cole. 1969. Conidium ontogeny in hyphomycetes. Trichothecium roseum and
its meristem arthrospores. Can. J. Bot. 47: 345-350.
255. Kendrick, W.B., G.T Cole, and G.C. Bhatt. 1968. Conidium ontogeny in hyphomycetes. Gonatobotryum
apiculatum and its botryose blastospores. Can. J. Bo!. 46: 591-596.
256. Leadbealer, Q., and C Mercer. 1957. Piptocephalis virginiana sp. nov. Trans. Brit, Mycol. Soc. 40; 461-471.
257. Lefebvre, C.L., and J.A. Stevenson. 1945. The fungus causing 7-onate leaf spot of cowpea. Mycologia
37: 37^15.
258. Lentz, PL. 1966. Dactylaria in relation to the conservation of Dactylaria. Mycologia 58: 965-966.
259. Lilly, V.G. and H.L. Barnett. 1951. Physiology of the Fungi. McGraw-Hill Book Co., New York.
260. Lilly, VG.and H.L. Barnett. 1953. The utilization of sugars by fungi. W Va. Agric. Expt. Sta. Bull. 362T.
261. Limber, D.R 1940. A new form genus of the Moniliaceae. Mycologia 32: 23-30.
262. Limber, D.R 1955. Studies in the genus Sporoncma. Mycologia 47: 389-402.
'
263. Linder, D.K. 1929. A monograph of the helio cos porous Fungi Imperfecti. Ann. Missouri Bot. Gard.
16: 227-388.
264. Linder. D.H. 1933. North American hyphomycetes I. Two new Helicosporeae and the new genera
Haplochalara and Paspalomyces. Mycologia 24: 342-348.
265. Linder. D.H. 1934. North American hyphomycetes II. New species and a new genus. Mycologia
26: 436-440.
266. Linder, D.H. 1937. New Venezuelan Fungi Imperfecti. Mycologia 29: 656-664.
267. Linder, D.H. 1942. A contribution toward a monograph of the genus Oidium. Uoydia 5: 165-207.
268. Linder, D.H. 1943. The genera Kickxella. Martemella. and Coemansia. Farlowia 1: 49-77.
269. Linder, D.H. 1943. New species of Sphaeropsidales and Melanconiales. Mycologia 35: 495-502.
270. Linneman, G. 1968. Ampleomyces quisqualis Ces. ein Parasit auf Mucorineen. Archiv fur Microbiol.
60: 59-75.
271. Luttrell, E.S. 1940. An undescribed fungus on Japanese cherry. Mycologia 32: 530-536.
272. Luttrell, E.S. 1963, Taxonomic criteria in Helminthosporium. Mycologia 5: 643-674.
273. Luttrell, E.S. 1964. Systematics of Helminthosporium and related genera. Mycologia 56: 119-132.
274. M a c L e o d , D . M . 1954. Investigations in the genera Beauveria Vuill.and Tritirachium Limber. Can. J. Bot.
32: 818-890.
275. Maciejowska, Z., and E.B. Williams. 1963. Studies on morphological forms of Staphylotrichum coccosporum. Mycologia 55: 221-225.
276. Madelin, M.F., and S. Dorabjee. 1974. Conidium ontogeny in Wallemia sebi. TYans. Brit. Mycol. Soc.
63: 121-130.
277. Mains, E.B. 1950. The genus Gibellula on spiders in North America. Mycologia 42: 306-321.
278. Mains, E.B. 1950. Entomogenous species of Aktmthomyces, Hymenostilbe, and Insecticola in North
America. Mycologia 42: 566-589.
279. Mains, E.B. 1951. Entomogenous species of Hirsutella. Tilachlidium, and Synnemaiium. Mycologia
43:691-718.
206
REFERENCES
280. Mangenot, F. 1952, Recherches methadiques sur les champignons de certains bois en decomposition.
Thesis, Faculty of Science, Nancy.
281. Mangenot, F. 1953. Sur quelque Hyphales dematiees lignicoles. Revue de Mycologie 18: 133-148.
282. Mason. E.W., and M.B. Ellis. 1953. British species of Perconia. Mycol. Papers C.M.I. 56: 1 - 1 2 7 .
283. Mason, E.W.. and S.J. Hughes. 1951. Phragmocephala gen. nov. hyphomcetarum. The Naturalist. JulySeptember. pp. 97-105.
284. McVey, D.V., and J.W. Gerdemann. 1960. The morphology of Lepiodiscus lerrislris and the function of
setae in spore dispersal. Mycologia 52: 193-200,
285. Mehrilich, F.R, and H.M. Fitzpatrick. 1935. Dichotomorphthora portulacae, a pathogene of Porfulaca
oleracea. Mycologia 27: 543-550.
286. Winter, D.W., and B.L. Brady. 1980. Mononematous species of Hirsuiella. Trans. Brit. Mycol. Soc.
74:271-282.
287. Winter, D.W., PM. Kirk, and B.C. Sutton. 1983. Thallic phialides. Trans. Brit. Mycol. Soc. 80: 39-66.
288. Misra, P C , and PH.B. Talbot. 1964. Phialomyces, a new genus of the hyphomycetes. Can. J. Bot- 42:
1287-1290.
289. Moore, R.T 1955. Index to the Helicosporae. Mycologia 47: 90-103.
290. Moore, R.T 1955. Index to the Helicosporae: addenda. Mycologia 49: 580-587.
.'
291. Moore, R.T 1958. Deuteromycetes I. The Sporidesmium complex. Mycologia 50: 681-692.
292. Moore, R.T 1959. The genus Piricauda (Deuteromycetes). Rhodora 61: 87-120,
293. Moore, R.T. 1959. The genus Berkleasmium. Mycologia 51: 734-739.
294. Morgan, D.J. 1971. Numerical taxonomic studies of the genus Botrytis 1. The B. cinerea complex. Trans.
Brit. Mycol. Soc. 56: 319-325.
295. Morgan, D.J. 1 9 7 1 . Numerical taxonomic studies of the genus Botrytis II. Other Botrytis taxa. Trans. Brit.
Mycol. Soc. 56: 327-335.
296. Morgan-Jones, G., TR. NagRaj, and B. Kendrick. 1972. Genera coelomycetarum V. Alkehesa and
Bartilinia. Canad. J. Bot. 50: 877-882.
297. Morgan-Jones, G., TR. NagRaj.and B. Kendrick. Icones genera coelomycetarum. Univ. of Waterloo Biology
Series. Waterloo, Ontario. (Published at intervals with illustrations.)
298. Morquer, R., G. Viala, J, Rouch, J, Fayret, and G. Berge. 1963. Contribution a l'etude morphogenique du
genre Gliocladium. Bull. Soc. Mycol. Fr. 79: 137-241.
.:•,
299. Morris, E.F. 1955. A new genus of Dematiaceae. Mycologia 47: 602-605.
300. Morris, E.F. 1956. Tropical Fungi Imperfecti. Mycologia 48: 728-737.
:
301. Morris, E.F. 1963. The synnematous genera of Fungi Imperfecti. Series in the biological sciences, No. 3
Western Illinois Univ., Macomb, 1 1 1 .
302. Morrison, R.H., and D.W. French. 1969. Taxonomy of cyllndrocladium flondanum and C. scoparium.
Mycologia 61: 957-966.
303. Morton, F.J,, and G. Smith. 1963. The genera Scopulariopsis Bainier, Microascus Zila, and Doratornyces
Corda. Mycol. Papers C.M.I. 86: 1-96.
304. Muthappa, B.H. 1973. Morphology of Stigmina ftcus-mysorensis sp. nov. Trans. Brit. Mycol. Soc.
61:602-605.
305. NagRaj, R.R., G. Morgan-Jones, and B. Kendrick. 1972. Genera coelomycetarum I V . Pseudorobillarda
gen. nov., a generic seggrate of Robillarda Sacc. Can. J. Bot. 50: 861-867.
306. Neergaard, P. 1945. Danish Species of Alternaria and Stemphyllium. Taxonomy, Parasitism, and
Economic Significance. Einar Munksgaard, Copenhagen.
307. Nelson, RE., and S. Wilheim. 1956. An undescribed fungus causing a root rot of strawberry. Mycologia
48: 547-551.
308. Nelson, R.R. 1964. The perfect stage of Curvularia geniculata. Mycologia 56: 777-779.
309. Nelson, R.R., and F.A. Hassis. 1964. The perfect stage of Curvularia lunata. Mycologia 56: 316-317.
310. Newhouse, J.R., and B.B. Hunter. 1983. Selective media for recovery of Cylindrocladium and Fusarium
species from roots and stems of tree seedlings. Mycologia 75: 228-233.
311. Nicot, J., and J. Meyer. 1956. Un hyphomycete noveau des sols tropicaux: Slaphylotrichum coccosporum
nov. gen. sp. Bull. Soc. Mycol. Fr. 72: 318-323.
312. Nicot, J., and M. Caillat. 1967. Etude morphologique d' une souche africainede Phialophora richardsiae
(Nannf.) Conant. Revue de Mycologie 32: 28-40.
1
•
•
REFERENCES
207
313. Nicot, J., arid F. Durand. 1965. Remarques sur la Moississure fongicolc Amblyosporium feoirvn's Fves.
Bull. Soc. Mycol. Fr. 81: 623-649.
314. Niedbalski, M., J.L. Crane, and D. Neely. 1979. Illinois fungi 10. Development, morphology and
taxonomy of Cristutariella pvramedialis. Mycobgia 71: 722-730.
315. Nyland, G. 1950- The genus Tiltetiopsis. Mycologia 42: 487^196.
316. Olive, L..S. 1948. Taxonomic notes on Louisiana fungi. Mycologia 40: 6-20.
317. Olive, L.S.. C.L. Lefebvre, and H.S. Sherwin. 1946. The fungus that causes sooty stripe of Sorghum spp.
Phytopathology 36: 190-200.
318. Omvik, A. 1970. Morphology and nutrition of Chloridium chlamydosporis (Bisporomyces chlamidosporis). Mycologia 62: 209-226.
319. Onions, A.H.S., and G.L, Barron. 1967. Monophialidic species of Paecilamyces. Mycol. Papers C.M.I.
107: 1-25.
320. Ostazeski, S.A. 1967. An undescribed fungus associated with a root and crown rot of birdsfoot trefoil
(Lows corniculaius). Mycologia 59: 970-975.
321. Papendorf, M.C., and H.P. Upadhyay. 1969. Boiryoderma laieritum and B. rostratum gen. et spp. nov,
from soil in Africa and Brazil. Trans. Brit. Mycol. Soc. 52: 257-265.
322. Parmelee, J. A. 1956. The identification of the Curvularia parasite of Gladiolus. Mycologia 48: 558-567.
323. Parmeter, J.R., H.S. Whitney, and W.D. Piatt. 1967. Affinities of some Rhizoclonia species that resemble
mycelium of Thanatephorus cucumeris. Phytopathology 57: 218-223.
324. Peck, C.A., and W.G. Solheim. 1958, The hyphomycetous genera of H.W Harknessand theascomycetous
genus Cleislosoma Harkn. Mycologia 50: 844-861.
325. Petch, T. 1930. Notes on entomogenous fungi. Trans. Brit. Mycol. Soc. 1 6 : 55-75.
326. Petch, T. 1943. British Nectroideae and allied genera. Trans. Brit. Mycol. Soc. 26: 53-70.
327. Peterson, R.H, 1962. Aquatic hyphomycetes from North America 1. Akuriosporae and key to genera.
Mycologia 54: 117-151.
328. Petersen. R.H. 1963. Aquatic hyphomycetes from North America 11. Akuriosporae and Blastosporae.
Mycologia 55: 18-29.
329. Pinkerton, M.E. 1936. A comparative study of the conidial formation in Cephalosporium and some
related hyphomycetes. Ann. Missouri Bot. Gard. 23: 1-68.
330. Pirozynski, K.A. 1962. Circinotrichum and Gyrolhrix. Mycol. Papers C.M.I. 84: 1 - 2 8 .
331. Pirozynski, K.A. 1963. Belirania and related genera. Mycol. Papers C M . I . 90: 1 - 3 7 .
332. Pirozynski, K.A, 1969. Reassessment of the genus Amblyosporium. Can. J. Bot. 47: 325-334.
333. Pirozynski, K.A., and R.A. Shoemaker. 1971. Some coelomycetes with appendaged conidia. Can. J,
Bot. 49: 529-541.
334. Pirozynski, K.A., and C.S. Hodges, Jr. 1973. Some new hyphomycetes from South Carolina. Can. J.
Bol.5\: 157-173.
335. Poitras, A.W. 1955. Observations on the asexual and sexual reproductive structures of the Choanephoraceae. Mycologia 47: 702-713.
336. Pollack, F.G. 1947. Two additions to the Fungi lmperfecti. Mycologia 39: 617-621.
337. Preslon, N.C. 1943. Observations on the genus Myroihecium 1. The three classic species. Tram. Brii.
Mycol. Soc. 26: 158-168.
338. Preslon, N.C. 1948. Myroihecium granineum Kub, and two new species. Trans. Brit. Mycol. Soc.
31; 271-276.
3 3 9 . Preston, N.C. 1 9 6 1 . Observations on the genus Myroihecium 1 1 1 . The cylindrical-spored species of
Myroihecium known in Britain. Trans. Brit. Mycol. Soc. 44: 31-41.
340. Puniihalingham, E. 1974. New species of Phomopsis- Trans. Brii. Mycol. Soc. 63: 229-236.
341. Punithalingam, E. 1974. Studies on Sphaeropsidales in Culture 11. Mycol. Papers C.M.I. 136: 1-63.
342. Punithalingam, E. 1975. Some new species and combinations in Phomopsis. Trans. Brit. Mycol. Soc.
64: 427-435.
343. Punithalingam, E. 1 9 7 9 . Graminicolous Ascochyta species. Mycol. Papers C.M.I. 1 4 2 : 1 - 1 2 4 .
344. Punithalingam, E. 1981. Studies on Sphaeropsidales in Culture III. Mycol. Papers C.M.I. 149: 1 - 4 1 .
345. Rakvidhyasastra, V„ and E.E, Butler. 1973. Mycoparasitism by Stephanoma phaeospora. Mycologia
65: 5H0-593.
346. Ranzoni, F.V. 1953. The aquatic hyphomycetes of California. Farlowia 4: 353-398.
/
/
/
t
7 0 8 REFERENCES
347. Rao, PR., and D. Rao. 1964. Some species of Camposporium Harkn. from India. Anionic van
Lee wen hoe k 30: 60-64.
348. Raper. K.B., and D.I. Fennel I. 1952. Two noteworthy fungi from Liberian soil. Amer. J. Boi. 39: 79-86,
349. Raper. K.E., and D.l. Fennell. 1965. The Genus Aspergillus. The Williams and Wilkins Co.. Baltimore.
350. Rawla, G.S. 1973, Gloeocercospora and Ramuli.spora in India. Trans. Brit. Mvcol. Soc. 60: 283-292.
352. Redhead, S.A. 1975. The genus Cristulariella von Hobnel. Can. J. Boi. 53: 700-707.
353. Reisinger, Otto. 1968. Remarques sur les genres Dendrvphielia et Dendryphion. Bull. Soc. Mycol. Fr.
84: 27-51.
354. Rifai, M. A. 1969. A revision of the genus Trkhoderma. Mycol. Papers C.M.I. 1 1 6 : 1-56.
355. Rifai, M.A.. and R.C. Cooke. 1966. Studies on some didymosparous genera of nematode-t rap ping
hyphomycetes. Trans. Brit. Mvcol. Soc. 49: 147-168.
356. Rogers, D.P 1959. On Ciccinobolus. Mycologia 51: 96-98.
357. Rogers, J.D. 1966. Notes on the conidial stage of Hypoxylon fuscuin. Mycologia 58: 459-465.
358. Routien, J.B. 1957. Fungi isolated from soils. Mycologia 49: 188-196,
359. Rudolph, B.A. 1931. Verticillium hydromycosis. Hilgariiia 5: 201-353.
360. Saccardo, PA. 1882-1931. Sylloge fungoruin omnium cognitorum. 25 volumes. Pa via, Italy.
361. Saksena, H.K., and O. Vaartaja. I960. Descriptions of new species of Rhizoctonia. Can. J. Bot.
38:931-943.
362. Saksena, S.B. 1955. A new fungus, Monicillium indicum gen. et sp. nov., from soil. Indian Phvtopath.
8: 9-12.
363. Salmon, E.S. 1904. On the identity of Ovulariopsis Patouillard and Hariot with the conidiat stage of
Phyllactinia Lev. Annates Mycol. 2: 438-444.
364. Salvin, S.B. 1949. Phase-determining factors in Blastomyces dermaiitklis. Mycologia 4\: 311-319.
365. Schoknecht, J.D., and J.L. Crane. 1977. Revision of Torula and Hormiscium species. Torula occulta,
T diverse, T elastkae, T. bigemina, and Hormiscium condensatum reexamined. Mycologia 69: 533-546.
366. Schol-Schwarz, M B . 1959. The genus Epicoccum Link. Trans. Brit. Mycol. Soc. 42: 149-173.
367. Seeler, E.V. 1943. Several fungicolous fungi. Farlowia I: 119-133.
36&. Shanor, L. 1946. A previusly undescribed fungus causing a leaf spot of bamboo. Mycologia 38: 33I-33S.
369. Shaw, C.G., and E.E. Hubert. 1952. A review of Lepiographium-Scopularia-Hantzxchia nomenclature.
Mycologia 44: 693-704.
370. Sherbakoff. C D . 1915. Fusaria on potatoes. Cornell Univ. Agr. Expt. Sta. Memoir No. 6.
371. Shigo, A.L. I960. Parasitism of Gonatobotrvum fuscum on species of Ceraiocystis. Mycologia
52: 584-598.
372. Shoemaker, R.A. 1959. Nomenclature of Drechslera and Bipolaris, grass parasites separated from
Helminthosporium. Can. J. Boi. 37: 879-887.
373. Shoemaker, R.A. 1962. Drechslera Ito. Can. J. Bot. 40: 809-836.
374. Shoemaker, R.A. 1964. Staining asci and annellophores. Stain Tech. 39: 120-121.
375. Shultz, E.S. 1916. Silver-scurf of the Irish potato caused bv Spondyiocladium atrovirens. Jour. Agr. Res.
6: 339-350.
376. Simmons, E.G. 1967. Typification of Aliernaria, Stemphylium and Vlocladium. Mycologia 59: 67-92.
377. Simmons, E.G. 1969. Perfect states of Stemphylium. Mycologia 6 1 : 1-26.
378. Simpson, F.W. 1946. Chromoblastomycosis. Some observations on the types of the disease in South
America. Mycologia 38: 432-499.
379. Smalley, E.B.,and H.N. Hansen. 1957. The perfect stage of Gliocladium roseum. Mycologia 49: 529-533.
380. Snell, W.H., and E.A. Dick. 1957. A Glossary of Mycology. Harvard Univ. Press, Cambridge. Mass.
381. Speare, A.T. 1912. Notes on Hawaiian fungi I. Gibellula su/fulta n. sp. Phytopathology 2: 135-137.
382. Speare, A.T. 1920. On certain entomogenous fungi. Mycologia 12: 62-76.
383. Sprague, R. 1938. Two Masiigosporium leaf spots on Gramineae. J. Agr. Res. 57: 287-299.
384. Sprague. R. 1943. The genus Phaesoptoria on grasses in the western hemisphere. Mycologia 35:483-491.
385. Sprague, R. 1948. Some leaf spot fungi on western Gramineae II. Mycologia 40: 177-193.
386. Sprague, R, 1950. Diseases of Cereals and Grasses in North America- The Ronald Press Company, New
York.
387. Sprague, R. 1951. Some leaf spot fungi on western Gramineae VI. Mycologia 43: 549-569.
388. Sprague, R. 1955. Some leaf spot fungi on western Gramineae VIII. Mycologia 47: 249-262. . " ''•
REFERENCES
209
389. Sprague. R., arid W.B. Cooke.
1939.
Some Fungi Imperfecti from the Pacific Northwest. Mycohgia
31:43-52.
1974.
Mycology Guidebook. University of Washington Press, Seattle.
390. Stevens, R.B., ed.
391. Steyaert, R,L.
1949.
Contribution a 1'etude monographique de Pestalolia de Not. et Monochaetia Sacc.
{Truncaiella gen. nov. et Pesialotiopsis gen. nov.) Bull. J a r d . Bot. Brux. 19: 285-354. - " > •
392. Steyaert. R.L.
1955. Pestalolia, Pesialotiopsis, et Truncaiella. Bull. Jard. Bot. Brux. 25: 191-199.
1963. The genus Chaelomeila. Trans. Brit. Mycol. Soc. 46: 409-425.
393. Stolk, A.C.
1937,
Phvmatoirichum (cotton or Texas) root rot in Arizona. Ariz. Agr. Expt. Sta. Tech.
394. Street, R.B,
Bull. 71.
395. Suhramanian, C.V. 1952. Fungi Imperfecti Madras I. Proc. Indian Acad. Sci. 36: 43-53.
396. Suhramanian, C.V. 1952. Fungi Imperfecti from Madras 11 and 111. Proc. Indian Acad. Sci, 36: 160-168;
223-228.
397. Suhramanian, C.V. 1953. Fungi Imperfecti from Madras IV. Proc. Indian Acad. Sci. 37: 96-105.
398. Suhramanian, C.V, 1953. Fungi Imperfecti fram Madras V. Curvuiaria. Proc. Indian Acad. Sci, 38:27-39,
399. Suhramanian. C.V. 1954. Three new hyphomycetes. Jour, Indian Bot. Soc. 33: 28-35.
400. Suhramanian, C.V.
1954. Fungi Imperfecti from Madras VI. Jour. Indian Bot. Soc. 3 3 : 36-42.
4 0 1 . Subramanian, C.V.
1955. Some species of Periconia from India. Jour. Indian Sol. Soc. 34: 339-361.
402. Subramanian, C.V.
403. Suhramanian, C.V. 1955. Fungi Imperfecti from Madras VII. Proc. Indian Acad. Sci. 4 3 : 283-291.
404. Subramanian, C.V, 1956. Hyphomycetes I. Jour. Indian Bot. Soc. 35: 53-91.
405. Subramanian, C.V. 1956. Hyphomycetes 11. Jour. Indian Bot. Soc. 35: 446-494.
406. Subramanian, C.V. 1957. Hyphomycetes IV. Proc. Indian Acad. Sci. 46: 324-335.
407. Subramanian, C.V.
1957.
Two new genera, Dwayahma and Sadasivania. Jour. Indian Bot. Soc. 36: 61-67,
408. Subramanian, C.V 1958. Hyphomycetes V. Jour. Indian Bui. Soc. 37: 47-64.
Indian Boi. Soc. 37: 1958.
Hyphomycetes VI. Two new genera. Edmundmasonia and lyegaria. Jour.
409. Subramanian, C.V. 401-407.
410. Subramanian. C.V. 1971. Hyphomycetes. Indian Coun. Agric. Res., New Delhi.
a n d K . . R a m a k r i s h n a n . 1956. AnlhasthoOpa, a new genus of the S p h a e r o p s i d a l e s .
4 1 1 . Proc. Indian Acad. Sci. 4 3 : 172-174.
Subramanian. C.B.. and K. Ramakrishnan.
1956.
On the genus Amphichaeia McAlpine. Jour. Indian
412. Bot. Soc. 35: 226-232.
Subramanian, C.V, and K.. Ramakrishnan.
1956.
CUiocharella Sydaw, Plagionema Subram. and
413. Ramakr., and Shanoria gen. nov. Trans. Brit. Mycol. Soc. 39: 314-318.
Subramanian, C.V, and K. Ramakrishnan.
1957.
Neotihspora Desm. and two new genera, Samukuia
414. and Sakireeia. Jour. Indian Bot. Soi'. 36: 6K-86.
Sumstine, D.R.
1911. Studies in North American hyphomycetes I. The genera Rhinoirichum and
415. Olpitrichum. Mycohgia 3: 45-56.
416. Sutton. B.C. 1961. Coleomycetes I. Mycol. Papers C.M.I. 80: 1-16.
Sutton, B.C.
1963,
Coleomycetes II. Neobarclaya, Mycohvpallage. Belptosporium, and Cryptosiictis.
417. Mycol. Papers C.M.I. 88: 1-50.
1964, Phoma and related genera. Trans. Brit. Mycol. Soc. 47: 497-509.
418. Sutton. B.C.
Sutton, B.C
1964.
Coleomycetes 111. Annellolacinia, Aristastoma, Phaeocytostroma, Seimalosporium.
Mycol. Papers C.M.I. 97: 1-42.
419.
Sutton, B.C.
1964.
Melamonium Link ex Fr. Persoonia 3: 193-198.
420.
Sutton, B.C.
1968.
Polynema, an earlier name for Neobarclaya. Mycohgia 60: 201-203.
421.
Sutton, B.C.
1969.
Forest microfungi I. Ampulliferina n. gen. n. sp. on leaves of the Labrador tea. Can. J.
Boi. 47: 609-616.
Coelomycetes IV. The genus Harknessia and similar fungi on Eucalyptus. Mycol.
422.
Sutton. B.C.
1971.
.
Papers C.M.I. 123: 1-46.
423. Sutton. B.C. 1973. Hyphomycetes from Manitoba and Saskatchewan, Canada. Mycol. Papers C.M.I.
132.
424. Sutton, B.C. 1973. Coelomycetes, p. 513-582, in The Fungi. IV A, Academic Press, New York.
425. Suiton, B.C. 1975. Coelomycetes V. Coryneum. Mycol. Papers C.M.I. 138.
426. Sutton. B.C.
1977. Coelomycetes VI. Nomenclature of generic names proposed for Coelomycetes. Mycol.
Papers C.M.I. 141: 1-253.
427. Sutton. B.C., and K.A. Pirozynski.
1965. Notes on microfungi II. Trans. Brii. Mycol. Soc. 48: 349-366.
2 1 0 REFERENCES
428. Swai, I.S., and D.F. Hindal. 1981. Selective medium for recovering Veriicicladietla prucera from soils and
symptomatic white pines. Plan! Disease 65: 963-965.
429. Swann, D.C., and H.L. Barnett. 1963. The effects of light on sporulation of Epicoccum nigrum. Proc. W.
Va. Acad. Sci. 35: 46-50.
430. Swift. M.E., and A.H.W. Povah. 1929. Contributions to a mycological flora of local soils. Mycologia
21: 204-221.
431. Taubenhaus. J.J. (916. SoiJ stain, or scurf, of sweet potato. Jour. Agr. Res. 5: 995-1002. ' .
432. Taubenhaus, J.J., and CM. Watkins, 1937. Phymatotrichum silvicolum n. sp.. its structure and development. American J. Bot. 24: 387-390.
433. Taylor, J.J. 1970. Further clarification of Sporotn'chum species. Mycologia 62: 797-825.
434. Tehon, L.R.
1937. Notes on the parasitic fungi of Illinois VI. Mycologia 29: 434-446.
435. Tehon, L.R. 1948. Notes on the parasitic fungi of Illinois. Mycologia 40: 314-327.
436. Thaxter. R. 1891. On certain new or peculiar North American hyphomycetes I. Oedocephalum,
Rhopatomyces, and Sigmoideomyces, n.g. Bot. Gaz. 16: 14-26.
437. Thaxter. R. 1891. On certain new or peculiar hyphomycetes II. Helicocephaium, Gonaiorrhodiella,
Desmidiophora, nov. gen., and Everharlia lignilalis n. sp. Bot. Gaz. 16: 201-205.
438. Thaxter, R. 1895. New or peculiar Zygomycetes 1. Dispira. Boi. Gaz. 20: 513-518.
439. Thaxter, R. 1897. New or peculiar Zygomycetes II. Syncephalastrum and Syncephalis. Bot. Gaz. 24: 1-15.
440. Thaxter, R. 1903. New or peculiar North American hyphomycetes III. Bui. Gaz. 35: 153-159.
441. Thaxter. R. 1914. New or peculiar Zygomycetes III. Blakeslea, Dissophora, and Haplosporangium, nova
genera. Bot. Gaz. 58: 353-366.
442. Thorn, C, and K.B. Raper. 1945. A Manual of the Aspergilli. The Williams and Wilkins Co., Baltimore.
443. 7'ogliani, F. 1952. Contributs alia conoscenza di uno sferossidale del genere Peyrolellaea. Annali dell
Spcrimentazione Agragia, Rome. N.S. 6: 81-94.
444. Toussoun, T.A., and RE. Nelson. 1968. A Pictorial Guide to the Identification of Fusarium Species.
Pennsylvania State University Press.
445. True, R.R, H.L. Barnett, C.K. Dorsey, and J.G. Leach. 1960. Oak will in West Virginia. W. Va. Agric.
Expt. Sta. Bull. 448T
446. Tubaki, K. 1952. Studies on Sporobolomycetaceae in Japan. Nagaoa 2: 62-66.
447. Tubaki, K. 1954, Studies on the Japanese Hyphomycetes 1. Coprophilous group. Nagoa A: 1-20.
448. Tubaki, K. 1955. Studies on Japanese hyphomycetes II. Funicoulous group. Nagoa 5: 11-40.
449. Tubaki. K. 1957. Studies on Japanese hyphomycetes III. Aquatic group. Bull. Natl. Sci. Museum (Tokyo).
No. 41. pp. 249-268.
450. Tubaki, K. 1958. Studies on Japanese hyphomycetes V. Leaf and stem group, with a discussion of the
classification of hyphomycetes and their perfect stages. Jour. Hattori Bot. Lab. No. 20.
451. Tubaki, K. 1963. Taxonomic study of Hyphomycetes. Ann. Rept. Inst. Fermentation, Osaka 1: 25-54.
452. Tubaki, K. 1963. Notes on Japanese hyphomycetes 1. Chloridium, Clonostachys, Isthmospora, Pseudohoirytis. Stachyhotrys, and Stephanoma. Trans. Mycol. Soc. Japan 4: 83-90.
453. Tubaki, K. 1964. Notes on the Japanese hyphomycetes II. Helicosporous group. Trans. Mycol. Soc.
Japan 5: 14.
454. Tullock, M. 1972. The genus Myrothecium Tode ex Fr. Mycol. Papers C.M.I. 130.
455. Uecker, F.A., WA. Ayers, and P.B. Adams. A new hyphomycete on sclerotia of Sclerotina sclerotiorum.
Mycotaxon 7: 275-282.
456. U.S.D.A. I960. Index of plant diseases in the United States. U.S. Government Printing Office, Washington. D.C.
457. Vanterpool, T.C. 1947. Selenophoma linicola sp. nov. on flax in Saskatchewan. Mycologia 39: 341-347.
458. Van Warmelo, K.T., and B.C. Sutton. 1981. Coelomycetes VII. Stegansporium. Mycol. Papers C.M.I.
145: 145.
459. Walker, J.C. and A.W. Minter.
1981. Taxonomy of Nemaiogonium, Gonatobotrvs, Gonatobotrvum. and
Gonaiorrhodiella. Trans. Brit. Mycol. Soc. 77: 299-319.
460. Wang, CJ.K. (965. Fungi of pulp and paper. New Vork State University College of Forestry Tech. PubJ.
87.
461. Wang. CJ.K. 1966. Annellophores in Torula jeanselmei. Mycologia 58: 614-621.
462. Wang, C.J.K., and G.E. Baker.
1967. Zygosporium masonii and Z. echinosporium from Hawaii. Can.
J. Bot. 45: 1945-1952.
,
,.,„.,
" •
REFERENCES
211
463. Wang, C.J.K.. and B.C. Sutton.
1982. New and rare lignicolous hyphomycetes. Mycologia 74; 489-500.
464. Waterman, A.M., and R.R Marshall.
1947,
A new species of Chstulariella associated with a leaf spot of
maple. Mycologia 39: 690-698.
465. Watson, P.
1955.
Calcarisporium arhuscula living as an endophyte in apparently healthy spirophores of
Russula and Laciarius. Trans. Brit. Mycol. Soc. 38:409-414.
466. Watson, P.
1965.
Further observations on Calcarisporium arhuscula. Trans. Bril. Mycol. Soc. 48: 9-17.
467. Webster. J.
1956.
Conidia of Acrospernntm compressum and A. gramineum. Trans. Bril. Mvcol. Soc.
39: 361-366.
46S. Wei, CI
1950.
Notes on Corynespora. Mycol. Papers C.M.I, 34: M 0 .
469. Whaley, J.W., and H.L. Barnett.
1963.
Parasitism and nutrition of Gonaioholrvs simplex. Mvcohgia
55: 195-210.
470. White, W.L,
1936.
A new species of Chondropodium on Pseudotsuga laxifolia. Mycologia 28: 433-438.
4 7 1 . White, W.L., and M.H. Downing,
1953. Humieola grisea, a soil-inhibiting cellulolytic hyphomycete.
Mycologia 4 5 : 951-963.
472. Wilson, E.E.
1949.
The pycnidial state of Exosporina fawceitii. Phytopathology 39: 340-346.
473. Wiltshire, S. P.
1938.
The original and modem concepts of Slemphvlium. Trans. Brit. Mvcol. Soc.
21:211-239.
474. Wolf, F.A.
1917.
A squash disease caused by Choanephora cucurbitarum. J. Agr. Res. 8: 319-328.
475. Wolf, F.A.
1935,
Morphology of Polythriniciurn causing sooty blotch of red clover. Mycologia 27: 58-73.
476. Wolf, F.A.
1938.
Life histories of two leaf-inhibiting fungi on sycamore, Mycologia 30: 54-63.
477. Wolf, F.A.
1949.
Two unusual conidial fungi. Mycologia 41: 561-564.
478. Wolf, F.A.,and R.W. Davison,
1941.
Life cycle of Piggotia fraxini, causing leaf disease of ash. Mvcohgia
33: 526-539.
479. Yerkes. D.W,
1956.
Chaeioseploria wellmanii in Mexico. Mycologia 48; 738-740.
480. Zuck. R.K,
1946.
Isolates between Stachyhotrys and Memnoniella. Mycologia 38: 69-76.
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GLOSSARY
Definitions and Examples
Acicular: slender and pointed; needle-shaped. Ephelis, p. 184.
Acervulus: an erumpent, open, saucer-shaped fruit body, bearing conidiophores and conidia, characteristic of the Melanconiales.
Acropetal: chain of conidia having the youngest conidium at the apex. Monilia, p. 72; Cladosporium,
p. 106.
Allantoid: conidia somewhat curved.
Aleuriospore: see p. 42.
Amerospore: a one-celled conidium.
Anastomosis: fusion between hyphal branches to form a network. Rhizoctonia, p. 196.
Anneilate: conidial scars appearing as rings at apex region of conidiophore or conidiogenous cell due to
successive formation of terminal conidia. Scopulariopsis, p. 98; Spilocaea, p. 106.
Annellospore: see p. 42.
Arthrospores:
seep.4\.
Attenuated: drawn out, narrowed, more or less to a point. Alternaria, p. 132; Cercospora, p. 128.
Ba si petal: successive chain of conidia having the youngest conidium at the base. Oidium, p. 68;
Aspergillus, p. 94.
Biotrophic: a method by which some parasites obtain nutrients from living host cells. Calcarisporium
parasiticum, Gonatobotrys simplex.
Blastospore: see p. 42.
Botr yob last ospore: see p. 43.
Bulbil: a small number of cells aggregated into a sclerotiumlike structure. Papularia, p. 82.
Capitate: conidia formed into a more or less rounded head. Aspergillus, p. 94; Botrytis, p. 76.
Catenulate: conidia formed in chains of two or more. Monilia, p. 72; Cladosporium, p. 106.
Ch lam yd ospore: a thick-walled terminal or intercalary conidium formed from a previous cell. Also see
Aleuriospore. Chalaropsis, p. 90; Sepedonium, p. 82.
Circinate: recurved. Circinotrichum, p. 90; Gyrothrix, p. 90.
Clamp connection: a hyphal outgrowth connecting two adjacent cells of the mycelium, characteristic of
certain basidiomycetes. Sclerotium, p. 196.
Clavate: club-shaped, broader toward the apex.
Coenocytic: nonseptate, with multinucleate hyphae or segments.
Collarette: a cup-shaped structure or flaring apex of a phialide. Phialophora, p. 88; Chlohdium,
p. 88.
Conidiogenous cell: a cell or portion of a conidiophore bearing conidia (a sporogenous cell).
Cruciform: arranged in the form of a cross. Dictyoarthrinum, p. 134; Entomosporium, p. 194.
212
GLOSSARY
213
Cupulate: cup-shaped, deeper than saucer-shaped. Hainesia, p. 174; Dinemasporium, p. 172.
Deciduous: referring to conidia falling off naturally.,
Dehiscent: breaking open at maturity. Dothichiza, p. 172; Sporonema, p. 172.
Dendroid: branched, treelike. Trichoderma, p. 92.
Denticle: small to medium sized, sharp or blunt, toothlike projection on which conidia are borne.
Gonatobotrys, p. 76.
Dermatomycosis: a fungus disease restricted to the surface of the skin of man and animals.
Determinate: cessation of growth of a conidiophore when a terminal conidium is formed. Microsporum,
p. 116; Humkola, p. 84.
Dichotomous: forked, branched into two more or less equal arms. Dichobotrys, p. 78.
Dictyospore: conidium having both transverse and oblique septa. Ahernaria, p. 132; Steganosporium,
p. 194.
Didymosporc: a two-celled conidium.
Dimidiate: a half structure, or having one part smaller than the other. Actinopehe, p. 174; Lepiostroma,
p. 176.
Discoid: disc-shaped, flat, and circular.
Echinulate: with slight projections, usually pointed, on the surface of conidia or conidiophores. Torula,
p. 74; Heterosporium, p. 122.
Ellipsoid, Elliptical: a conidium having an outline of an ellipse with rounded ends. Pithomyces, p. 132;
Bactridium, p. 148.
Endogenous: conidia produced well within a phialide. Chalara, p. 90.
Erumpent: breaking out through the surface of the substratum. Coryneum, p. 194; Botryodipiodia,
p. I S O .
Exogenous: conidia produced on the outside of a conidiogenous cell.
Falcate: curved like the blade of a sickle.
Falx: a hook-shaped hypha or cell capable of bearing conidia. Zygosporium, p. 72.
Fascicle: tight cluster or group. Graphium, p. 152; Doratomyces, p. 154.
Filiform: threadlike, very slender. Septoria, p. 182; Cylindrosporium, p. 192.
Flexuous: wavy. Polythrincium, p. 112.
Fusoid, Fusiform: spindle-shaped. Microsporum, p. 1 1 6 ; Monacrosporium, p. 1 1 8 .
Fuscous: brownish-gray, smoky.
Geniculate: bent like a knee, often giving a zig-zag appearance. Geniculosporium, p. 100.
Globose: nearly spherical.
Haustorium: a special absorbing structure formed by some parasitic fungi within cells of the host.
Piptocephalis, p. 62.
Helicospore: a coiled or spiral-shaped conidium. Helicomyces, p. 136.
Hyaline: clear, absence of dark pigment.
Hyperparasite: a parasite on another parasitic fungus. (A term used loosely; often, parasitism has not
been proved.) See also Mycoparasite.
Hyphopodium: a 1- or 2-celled, branchlike structure on epiphytic mycelium of certain fungi.
214
GLOSSARY
Clasterosporium, p. 118.
Hysteriform: elongated, with a median cleft. Leptostroma, p. 176.
Indeterminate: growth of conidiophore does not cease with production of a terminal conidium or group
of conidia. Gonatobotrys, p. 76; Curvularia, p. 122.
Innate: immersed in substratum. Sphaeropsis, p. 176; Cytospora, p. 170.
Intercalary: produced between other cells, not terminal.
Lenticular: in the form of a double convex lens.
Locule: a cavity, usually within a stroma. Dothiorella, p. 166; Cytospora, p. 170.
Lunate: crescent-shaped, like a half moon. Lunulospora, p. 138.
Macroconidia: large, often multicelled conidia, applied when fungus produces conidia of two distinct
sizes. Fusarium, p. 130.
Meristem arthrospore: see p. 41.
Microconidia: small, usually 1-celled conidia, often applied to spermatia.
Muriform: conidia with both an oblique septa and a dictyopore. Alternaria, p. 132; Steganosporium,
p. 194.
Murogenous: originating as an expansion of the entire conidiophore tip. Murogenella, p. 114.
Mycoparasite: a fungus parasitic on another fungus. Gonatobotrys, p. 76; Piptocephalis, p. 62.
Necrosis: death of cells; often applied to host of a micoparasite.
Obclavate: inversely clavate, widest at base.
Oblong: about twice as long as wide, usually with blunt ends.
Obovoid: inversely ovoid, narrowest at base.
Ostiole: opening or mouth of a pyenidium. Phoma, p. 162.
Ovoid: egg-shaped, with narrower end at apex.
Papilla: a small rounded projection.
Pedicel: a short, slender stalk bearing a conidium. Brachysporium, p. 126.
Penicillus: a brush, referring to compactly branched conidiophores. PeniciUium, p. 94; Gliocladium,
p. 92.
Penicillate: a brushlike cluster of sporogenous cells on a conidiophore as in PeniciUium, p. 94.
Percurrent: proliferation of conidiophore or conidiogenous cell in which each successive apex arises
through the previous apex. Gonatobotrys, p. 76; Spilocaea, p. 106.
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Phialide: a specialized sporogenous cell producing conidia from an open end in basipetal succession.
Chalara, p. 90; Phialocephala, p. 96.
Phialospore: see p. 44.
Phragmospore: a several-celled conidium with transverse septa only. Bipolaris, p. 126; Dendryphiopsis,
p. 120.
Pigmented: used to indicate presence of pigment in the cell waifs, not in the internal contents.
Polyphialide: a phialide with more than one open end.
Porospore: see p. 43.
Pseudoparenchyma: isodiametric or oval fungus cells organized into tissues in which the individual
hyphae have lost their identity. Sclerotium, p. 196.
GLOSSARY
215
Pycnidium: a closed or nearly closed asexual fruit body bearing conidiophores and conidia internally,
characteristic of the Sphaeropsidales.
Pyriform: pear-shaped, narrower at the base.
Rachis: central axis of a conidiophore on which conidia are attached alternately. Tritirachiwn, p. 100. ,
Reniform: kidney-shaped.
Sclerotium: a compact resistant mass of hyphae or pseudoparenchyma.
Scolecospore: a long slender conidium. Septoria, p. 182; Cylindrosporium, p. 192.
Sessile: without a stalk. Tripospermum, p. 142; Aureobasidium, p. 70.
Seta: a sterile hypha associated with various fruiting structures. Colletotrichum, p. 188; Gyrothrix,
p. 90.
Sporangiole: a small sporangium producing one to few spores, characteristic of some Mucorales.
(In some genera the 1-celled sporangioles may be called conidia.) Choanephora, p. 66.
Sporocladium: a special short branch of a sporangiophore in certain Mucorales in which conidia are
borne on one side only. Martensella, p. 64.
Sporodochium: a cushion-shaped structure made up of closely grouped conidiophores, characteristic of
the Tuberculariaceae.
Sporogenous cell: a special cell or branch bearing conidia.
Staurospore: a branched or star-shaped conidium. Tridenteria, p. 140; Tripospermum, p. 142.
Sterigma: a short, pointed, peglike extension of a cell that supports a conidium, usually considered larger
than a denticle.
Stipirate: having a stipe or stalk. Cornularia, p. 186.
Stroma: a compact mass of hyphae on which or in which conidia or fruit bodies are borne.
Botryodiplodia, p. 180; Cytospora, p. 170.
Stylospore: an elongated conidium produced in a pycnidium. Phomopsis, p. 164.
Subhyaline: conidia generally classified as hyaline, but showing slight pigmentation in mass.
Subiculum: a loose crustlike growth on which fruit bodies are produced. Asteromella, p. 164.
Sympodulospore: see p. 43.
Sympodial: growth or branching of a conidiophore or sporogenous cell arising beneath or behind the
previous conidium and pushing it to one side. Curvularia, p. 122; Triiirachium, p. 100.
Synnema: a cylindrical compact group of conidiophores, characteristic of the Stilbaceae.
Torulose: cylindrical but having swellings at intervals.
Truncate: cut off at the end, flat. Scopulariopsis, p. 98; Geotrichum, p. 68.
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Verricose: having small rounded processes, appearing as a minutely roughened wall. Ulocladium, p. 132;
Periconia, p. 74.
Verticillate: having a whorl of three or more branches or sporogenous cells arising at the same
level. VerticilHum, p. 92,
Vesicle: an inflated cell or portion of conidiophore. Cylindrocladium, p. 108.
Whorl: a number of conidia or branches attached at the same level. VerticilHum, p. 92.
INDEX TO GENERA
Acarocybe, 158
Acladium, 76
Acrospeira, 132
Acrosporium, see Oidium
Actinopelte, 174
Actinospora, 140
Aegerita, 150
Akanthomyces, 158
Alatospora, 142
-Alternaria, 132
Amblyosporium, 68
Amerosporium, 172
Ampelomyces, 166
Ampulliferina, 106
Anguillospora, 140
Annellophora, 1 1 8
Anthasthoopa, 174
Aposphaeria, 162
Aristatoma, 180
Arthrinium, 74
Arthrobotrys, 110
Arthrobotryum, 154
Arthrosporium, 154
Articulospora, 142
Aschersonia, 174
-Ascochyta, 1 7 8
-Aspergillus, 94
Asperisporium, 1 1 2
Aster omella, 164
Asteromyces, 84
Asterosporium, 194
Aureobasidium, 70
Bactridium, 148
Bactrodesmium, 150
Balanium, 106
Bartilinia, 182
Basidiobotrys, 100
Basipetospora, 70
Beauveria, 100
Beltrania, 104
Berkleasmium, 134
Bipolaris, 126
Bispora, 106
Bisporomyces, see Chloridium
Blastomyces, 80
Botryoderma, 86
- Botryodiplodia, 180
Botryosporium, 76
Botryotrichum, 84
-Botrytis, 76
Brachysporium, 1 2 6
Briosia, 152
Cacumisporium, 124
Calcarisporium, 102
Camarosporium, 1 8 6
Camposporium, 1 1 6
Camptomeris, 1 5 0
Candelabrella, 110
Candida, 70
Catenophora, 188
Catinula, 172
Cephaliophora, 1 1 6
Cephalosporium, 94
Ceratophorum, 118
Ceratosporella, 144
Ceratosporium, 144
-=Cercospora, 128
Cercosporella, 128
Cercosporidium, 122
Chaetochalara, 90
Chaet omella, 176
Chaetophoma, 164
Chaetopsina, 96
Chaetopsis, 96
Chaetoseptoria, 184
Chalara, 90
Chalaropsis, 90
Cheiromyces, 150
Chlamydomyces, 82
Chloridium, 88
Choanephora, 66
Chondropodium, 186
Chromelosporium, 80
Chrysosporium, 68
Cicinnobolus, see Ampelomyces
Circinotrichum, 90
Cladobotryum, 1 0 8
Cladosporiella, 92
—Cladosporium, 106
Clasterosporium, 1 1 8
Clavariopsis, 140
Codinaea, 88
Coemansia, 62
—Colletotrichum, 188
Coniosporium, 134
Coniothyrium, 176
Conoplea, 102
Cordana, 112
Cornularia, 186
Corynespora, 120
— Coryneum, 194
Cristulariella, 74
Cryptosporium, 190
Culicidospora, 1 4 0
Cunmnghamella, 60
216
Curvularia, 122
Cylindrocarpon, 1 3 0
Cylindrocladium, 1 0 8
Cylindrosporium, 192
Cytospora, 1 7 0
Cytosporella, 1 7 0
Cytosporina, 166
Dactylaria, 110
Dactylella, 128
Dactylium, 130
Dactylosporium, 134
Darluca, 178
Deightoniella, 1 1 8
Dendrodochium, 146
Dendrographium, 154
Dendrophoma, 162
Dendrospora, 140
Dendryphion, 124
Dendryphiopsis, 120
Dichobotrys, 78
Dichomera, 186
Dichotomophthora, 120
Dicranidion, 1 3 8
Dictyoarthrinium, 134
Dictyosporium, 144
Didymaria, 1 1 0
Didymobotryum, 156
Didymostilbe, 154
Dilophospora, 166
Dimargaris, 62
Dinemasporium, 1 7 2
Diplocladiella, 142
Diplococcium, 1 1 4
-Diplodia, 180
Diplodina, 178
Diplosporium, 108
Discosia, 182
Dispira, 66
Doratomyces, 154
Dothichiza, 172
-Dothiorella, 166
Dothistroma, 180
Drechslera, 122
Dwayabeeja, 1 1 6
Echinobotryum, 84
Eleutheromycella, 168
Eleutheromyces, 1 6 8
Endocalyx, 152
Endophragmia, 118
—Entomosporium, 194
Ephelis, 184
INDEX
Epicoccum, 150
Everhartia, 150
fexcipularia, 148
Exosporium, 148
Flagellospora, 138
Fusariella, 130
Fusarium, 130
Fusicladium, 1 1 2
Fusicoccum, 170
Fusoma, 1 1 6
Gelatinosporium, 182
Genicularia, 1 1 0
Geniculosporium, 100
Geotrichum, 68
Gibellula, 160
Gilmaniella, 84
Gliocephalis, 94
Gliocephalotrichum, 94
Gliocladium, 92
Gliomastix, 86
Gloeosporium, 188
Glomerularia, 86
Gonatobotrys, 76
Gonatobotryum, 78
Gonatophragmium, 122
Gonatorrhodiella, 78
Gonytrichum, 98
Graphium, 152
Gyrothrix, 90
Hadrotrichum, 146
Hainesia, 174
Hansfordia, 98
Haplographium, 80
Haplosporella, 178
Harknessia, 176
Harpographium, 156
Helicocephalum, 60
Helicodendron, 136
Helicoma, 136
Helicomina, 136
Helicomyces, 136
Helicoon, 136
Helicosporium, 136
Heliscus, 108
- Helminthosporium, 124
Hendersonia, 184
Hendersonula, 180
Heterocephalum, 152
Heterosporium, 122
Hirsutella, 160
Hirudinaria, 144
Histoplasma, 82
Hobsonia, 150
Humicola, 84
Hyalodendron, 72
Hyalopycnis, 168
Hymenella, 146
Hymenostilbe, 158
Idriella, 102
Illosporium, 146
Ingoldia, 138
Insecticola, 158
lsaria, 156
Isariopsis, 154
Itersonilia, 70
Kellermania, 178
Kickxella, 64
Lacellina, 78
Lacellinopsis, 78
Lemonniera, 138
Leptographium, 98
Leptostroma, 176
Leptostromella, 184
Leptothyrium, 174
Libertella, 190
Linderina, 64
Lunulospora, 138
Macrophoma, 164
Mammaria, 84
-Marssonina, 190
MartehsSlla, 64 '
Martens iomyces, 64
Melanconium, 190
Melasmia, 174
Memnoniella, 88
Menispora, 88
Menisporopsis, 152
Metarrhizium, 94
Microclavia, 80
Micr opera, 182
Microsporum, 1 1 6
Monacrosporium, 1 1 8
"Monilia, 72
Monilochaetes, 86
Monochaetia, 192
Monocillium, 86
Mortierella, 60
Murogenella, 114
Mycogone, 82
Mycoleptodiscus, 190
Mycotypha, 60
Myrothecium, 146
Nakataea, 128
Neottiospora, 166
Nigrospora, 82
Nodulosporium, 100
Oedocephalum, 76
Oidiodendron, 68
Oidium, 68
Olpitrichum, 74
Ovularia, 104
Ovulariopsis, 70
Paecilomyces, 94
Papularia, 82
Papulospora, 196
Passalora, 1 1 2
--Penicillium, 94
Periconia, 74
Periconiella, 104
Pesotum, 152
— Pestalotia, 192
Pestalozziella, 188
Peyronellaea, 164
Phaeoseptoria, 184
Phialocephala, 96
Phialomyces, 94
Phialophora, 88
Phleospora, 186
Phlvctaena, 186
"-Phoma, 162
-^Phomopsis, 164
Phragmocephala, 1 1 8
Phragmotrichum, 194
Phyllosticta, 162
Phymatotrichum, 78
Piptocephalis, 62
Pithomyces, 132
Pleiochaeta, 128
Plenodomas, 162
Pleurophragmium, 126
Pleurostromella, 170
Pleurothecium, 126
Podosporium, 154
Polynema, 192
Polythrincium, 112
Prosthemium, 186
Pseud obotrytis, 106
Pseudotorula, 1 1 6
Pucciniopsis, 148
Pyrenochaeta, 162
Pyricularia, 128
Rabenhorstia, 170
Radiomyces, 64
Ramularia, 110'
Ramulispora, 148
Rhabdospora, 184
Rhinocladiella, 104
Rhinotrichum, 76
^—Rhizoctonia, 196
Rhizosphaera, 164
Rhopalomyces, 60
Rhynchophoma, 178
Rhynchosporium, 108
Robillarda, 178
Sclerographium, 158
Sclerotiopsis, 166
"Sclerotium, 196
Scolecobasidium, 1 1 4
217
218
INDEX
Scolecotrichum, 112
Scopulariopsis, 98
Seimatosporium, 192
Selenophoma, 162
Selenosporella, 102
Sepedonium, 82
Septocylindrium, 128
Septogloeum, 190
Septonema, 116
-Septoria, 182
Shanoria, 172
Sirosporium, 134
Spadicoides, 114
Spegazzinia, 150
Speiropsis, 142
Spermospora, 128
Sphacelia, 148
-Sphaceloma, 188
Sphaerographium, 184
Sphaeronaema, 168
. Sphaeropsis, 176
Sphaerosporium, 146
Spilocaea, 106
Spirodactylon, 64
Spiromyces, 66
Spiropes, 158
Spondyiocladiella, 120
Sporidesmium, 120
Sporobolomyces, 70
Sporonema, 172
,
Sporoschisma, 130
Sporothrix, 98
Stachybotrys, 88
Stachylidium, 92
Stagonospora, 180
Staphylotrichum, 80
Steganosporium, 194
Stemphylium, 132
Stephanoma, 82
Stigmella, 134
Stigmina, 120
Stilbum, 152
Strumella, 146
Sympodiella, 104
Syncephalastrum, 66
Syncephalis, 62
Synnematium, 160
Tetrachaetum, 140
Tetracladium, 1 4 0
Tetranacrium, 182
Tetrapola, 142
Thallospora, 142
Tharoopama, 156
Thielaviopsis, 92
Thysanophora, 96
Tieghemiomyces, 62
Tilletiopsis, 72
Torula, 74
TrichocladLum, 1 1 8
Trichoderma, 92
Trichophyton, 1 1 6
Trichothecium, 108
Trichurus, 156
Tricladium, 138
Tridentaria, 140
Tripospermum, 142
Triposporium, 144
Triscelophorous, 1 3 8
Tritirachium, 100
Tubercularia, 146
Tuberculina, 1 4 8
Ulocladium, 132
Umbelopsis, 86
Varicosporium, 1 3 8
Verticicladiella, 104
Verticicladium, 104
—-Verticillium, 92
Virgaria, 100
Volutella, 1 4 8
Wallemia, 92
Wardomyces, 84
Xenosporium, 136
Zygosporium, 72