MORPHOLOGY OF CHAETOMIUM ERRATICUM

Development of perithecia from single, uninucleate ascospores disclosed a homothallic condition for Chaetomium erraticum. This species was found to produce sessile ascogonial coil initials from uninucleate vegetative cells that become enveloped by hyphae formed at the base of the ascogonium. The ascogonium consists of several cells that are uninucleate or binucleate. A perithecium forms from numerous divisions and enlargement of the surrounding uninucleate cells. Differentiation of the perithecial cells results in the formation of a carbonaceous wall, perithecial hairs, and an ostiole lined with periphyses. A convex hymenial cluster of ascogenous cells forms in the lower half of the centrum from which typical croziers develop. Asci push up into the pseudoparenchyma cells of the centrum. The growth of the ascogenous system is in part responsible for increase in perithecial size. The breakdown of the pseudoparenchyma cells around the developing asci results in the formation of a central cavity in which ascospores are released when the asci deliquesce. No paraphyses are present. The type of development and features of the centrum of C. erraticum and other species of Chaetomium indicate a distinct Xylaria-type centrum.     

Perithecium morphogenesis in Sordaria macrospora

The perithecium of the self-fertile ascomycete Sordaria macrospora provides an excellent model in which to analyse fungal multicellular development. This study provides a detailed analysis of perithecium morphogenesis in the wild type and eight developmental mutants of S. macrospora, using a range of correlative microscopical techniques. Fundamentally, perithecia and other complex multicellular structures produced by fungi arise by hyphal aggregation and adhesion, and these processes are followed by specialization and septation of hyphal compartments within the aggregates. Perithecial morphogenesis can be divided into the ascogonial, protoperithecial, and perithecial stages of development. At least 13 specialized, morphologically distinct cell-types are involved in perithecium morphogenesis, and these fall into three basic classes: hyphae, conglutinate cells and spores. Conglutinate cells arise from hyphal adhesion and certain perithecial hyphae develop from conglutinate cells. Various hypha-conglutinate cell transitions play important roles during the development of the perithecial wall and neck.     

Studies on the development of perithecium of Ceratocystis stenoceras

The development of the perithecium of Ceratocystis stenoceras was observed by a light microscope and by a scanning electron microscope.The fungus has developed dark brown perithecia on wheat agar medium in three days of incubation. Perithecial primordia appeared as tightly knotted coils. At the center of it an oval ascogonium was observed. The ascogonium was developed from a lateral wall of a hypha, and the hyphae covering the ascogonium branched at the basal part where the ascogonium was attached. These hyphae branched repeatedly in the developmental growth to cover the ascogonium, and it was finally covered tightly. The plasmogamy of this fungus is much probably performed by the gametangial contact. As the stage proceeded, the ascogonium elongated, the terminal and the basal portions of it swelled and cleavage of the ascogonium resulted. Each of the cleaved ascogonia germinated continuously and stretched out the ascogenous hyphae. About that time the cells consisting of perithecia were vacuolated from the center and successively dissolved, so that a space was formed in the center of the body. Ascogenous hyphae continued to develop downwards, and their end were fixed to the inner wall of the body.The upper portion of the hyphae converged to the center of the body and the ascogenous hyphae became the supporting tissue for ascus formation.Hook formation was observed prior to the ascus formation. After completion of karyogamy by hook formation, the fissure appeared on the ascus and the end portion was released. The released portion included eight ascospores. The ascus had a smooth surface and no special structure was seen on the top. As the asci were matured, they evanesced by themselves and concurrently ascospores came out. Finally the body was massively filled with ascospores.     

PERITHECIAL FORMATION IN GELASINOSPORA RETICULISPORA. I. EFFECTS OF LIGHT AT TWO DIFFERENT GROWTH STATES

Hyphae of Gelasinospora reticulispora were cultured on corn meal agar in a growth tube at 25 ± 0.4°C under different light conditions. While the hyphal tip was growing, perithecia were not formed under continuous white light (ca. 2000 ergs cm^?2 sec^?1), but some perithecia were initiated in total darkness. However, when white light was given after a dark period, perithecial formation was greatly promoted. In these cases, perithecial formation occurred in older portion of the culture (the portion nearest the point of inoculation) at first, and then gradually spread to the younger portion. Immediately after the tip of hyphae reached the other end of the growth tube, perithecia were induced in the youngest portion of the hyphae irrespective of the photoconditions; then formation proceeded toward the older portion. This induction was not age-dependent, because in growth tubes with different lengths, perithecia always became visible ca. 24 hr after the tip of hyphae reached the other end of growth tube. The photoinhibitory effect was no longer observed thereafter, but photopromotive effect was still evident.     

Freshwater ascomycetes: Jahnula apiospora (Jahnulales, Dothideomycetes), a new species from Prince Edward Island, Canada

A new ascomycete species, Jahnula apiospora (Jahnulales, Dothideomycetes), collected from submerged wood in a freshwater creek on Prince Edward Island, Canada, is described and illustrated. The characteristic features of the new species are globose to subglobose, black, ostiolate, membranous ascomata with broad, brown, subtending hyphae; a peridial wall composed of an outer layer of thick-walled cells occluded by black, amorphous material along the upper two-thirds of the ascoma; trabeculate pseudoparaphyses; cylindrical to narrowly fusoid, fissitunicate asci; and brown, one-septate, apiosporous ascospores without a gelatinous sheath or appendages.     

Perithecial ascomycetes from the 400 million year old Rhynie chert: an example of ancestral polymorphism

We describe a perithecial, pleomorphic ascomycetous fungus from the Early Devonian (400 mya) Rhynie chert; the fungus occurs in the cortex just beneath the epidermis of aerial stems and rhizomes of the vascular plant Asteroxylon. Perithecia are nearly spherical with a short, ostiolate neck that extends into a substomatal chamber of the host plant; periphyses line the inner surface of the ostiole. The ascocarp wall is multilayered and formed of septate hyphae; extending from the inner surface are elongate asci interspersed with delicate paraphyses. Asci appear to be unitunicate and contain up to 16 smooth, uniseriate-biseriate ascospores. The method of ascospore liberation is unknown; however, the tip of the ascus is characterized by a narrow, slightly elevated circular collar. Ascospores appear 1-5 celled, and germination is from one end of the spore. Also present along the stems and interspersed among the perithecia are acervuli of conidiophores that are interpreted as the anamorph of the fungus. Conidiogenesis is thallic, basipetal and probably of the holoarthric-type; arthrospores are cube-shaped. Some perithecia contain mycoparasites in the form of hyphae and thick-walled spores of various sizes. The structure and morphology of the fossil fungus is compared with modern ascomycetes that produce perithecial ascocarps, and characters that define the fungus are considered in the context of ascomycete phylogeny.     

ULTRASTRUCTURE OF ASCOCARP DEVELOPMENT IN SPORORMIA AUSTRALIS

Thin sections taken from intact ascocarps were examined to trace the developmental sequence of ascocarp formation in Sporormia australis Speg. The ascocarp originated from a uninucleate vegetative hyphal cell which underwent repeated divisions and formed an ascostroma. In the center of the young ascostroma a cavity formed, apparently from cell disintegrations, and enlarged as the ascocarp enlarged. Within the cavity pseudoparaphyses developed from undifferentiated pseudoparenchymatous cells at the apex of the cavity and extended downward. Ascogenous hyphae arose from proliferating uninucleate cells at the base of the cavity. As the ascocarp matured, the pseudoparenchymatous cells differentiated into three layers, none of which were considered homologous to the perithecial wall lining the cavity of pyrenomycetes. The cells of the apex were not differentiated into layers and light microscopy revealed the presence of an ostiole through which bitunicate asci discharged their eight 4-celled ascospores.     

小煤炱科子囊壳超微结构研究

用扫描电镜对小煤炱科Meliolaceae的美座附丝壳Appendiculella calotroma(Desm.)Hoehnel和莫勒针壳炱Irenopsis molleriana(Wint.)Stev.的子囊壳进行观察的结果,发现它们的子囊壳都有一个小孔口,孔口周围有2～4层小圆柱形至椭圆形细胞;它们的子囊壳表面细胞呈疣状或乳突状,具纵向沟纹。其中美座附丝壳还有具横条纹的蠕虫状附属物,莫勒针壳炱有光滑的子囊壳刚毛。子囊壳表面孔口的发现为小煤炱目Meliolales的确立提供了直接的证据。     

DEVELOPMENT OF THE PERITHECIUM IN GNOMONIA COMARI (DIAPORTHACEAE)

Perithecia of Gnomonia comari (Ascomycetes) mature within 14 days on cornmeal agar under continuous fluorescent light at 25 C. The perithecium is initiated by a coiled, multicellular ascogonium. Branches from somatic hyphae surround the ascogonium. This hyphal envelope early differentiates into two regions: a centrum of pseudoparenchymatous cells and a peripheral wall of more elongated, flattened cells. The wall produces a long, ostiolate beak by eruption of a column of hyphae from the inner layers at the apex; the cells gradually become thick-walled and brown from the peripheral layers inward. Proliferations from the ascogonial cells near the center of the perithecium form a bowl-shaped mass of ascogenous hyphae which expands centrifugally until it appears in section as a crescentic layer across the middle of the centrum. The centrum pseudoparenchyma above this incipient hymenium disintegrates, and short abortive paraphyses extend upward from the subhymenial pseudoparenchyma into the resulting cavity. The paraphyses disintegrate as the asci develop among them. The hymenium gradually pushes downward into the disintegrating subhymenial pseudoparenchyma until it rests on the perithecial wall. Maturing asci become detached from the hymenium, fill the perithecial cavity, and pass through the ostiole. At the tip of the beak they discharge their ascospores forcibly. Diaporthaceae with abortive paraphyses may occupy an intermediate position in a series leading from forms (Gaeumannomyces graminis) with long delicate paraphyses resembling those in the Sordariaceae to forms (Stegophora ulmea) in which the centrum is entirely pseudoparenchymatous.     

A new species ofNannizziopsis from New Jersey soil

Nannizziopsis mirabilis, isolated from a soil sample collected from New Jersey, USA, is described as a new species. The ascomata are white to pale yellow, with a peridium of a network of loosely interwoven hyphae and simple, more or less straight, clavate appendages. The ascospores are hyaline, globose to subglobose, and ornamented with spiral bands or sometimes polygonal pits. The associated anamorph is assignable to the form genusChrysosporium.     

STUDIES IN THE GENUS NECTRIA. II. MORPHOLOGY OF N. GLIOCLADIOIDES

Hanlin , Richard T. (Georgia Experiment Station, Experiment.) Studies in the genus Nectria. II. Morphology of N. gliocladioides. Amer. Jour. Bot. 48(10): 900–908. Illus. 1961.—Swollen tips of vegetative hyphae develop into multicellular archicarps from which multinucleate ascogonia form. From basal cells of each archicarp arise hyphae which grow up into a prosenchymatous, true perithecial wall; around this wall is formed a thin pseudoparenchymatous stroma of compacted hyphae. The ascogonia give rise to ascogenous cells from which croziers and asci form directly. At the same time, an apical meristem forms cells that grow downward into the centrum. These are pseudoparaphyses. Asci grow up among the pseudoparaphyses, which deliquesce as the ascocarp matures. The ascus tip contains a thick ring with a pore and lateral thickening of the ascus wall. Ascospores are forcibly ejected. The chromosome number is 4. This species conforms to the Nectria Developmental Type of Luttrell.     

Freshwater ascomycetes: <Emphasis Type="Italic">Aliquandostipite minuta</Emphasis> (Jahnulales,Dothideomycetes), a new species from Florida

An undescribed ascomycete similar to species in the Aliquandostipitaceae (Jahnulales, Dothideomycetes) was collected from submerged wood in a freshwater swamp in Big Cypress National Preserve, Florida. The characteristic features of the new species are as follows: (i) ascomata are small, sessile, light brown, globose to subglobose, papillate, and anchored to the substrate by wide, brown, septate and subtending hyphae; peridial wall is composed of 1 to 2 layers of large, angular cells with large lumens; (ii) asci are ovoid to broadly clavate, and fissitunicate; (iii) ascospores are one-septate, fusiform, multiguttulate, pale brown, surrounded by a fusiform gelatinous sheath, and equipped with numerous filamentous appendages around the midseptum. The new fungus is most similar to Aliquandostipite crystallinus, from which it differs in overall smaller size and morphology. This new fungus is described and illustrated herein as A. minuta.     

Nutrient-dependent inhibition of perithecial development due to sequential crosses on the same mycelium of Neurospora tetrasperma

Summary An explanation of perithecial inhibition in the second of two sequential crosses at different locations on the same mycelium of Neurospora tetrasperma was sought by (1) assaying media that had supported inhibited and uninhibited portions of the mycelium which contained no developing perithecia, (2) determining the effect of these media on perithecial development, (3) adding nutrients to inhibited portions of the mycelium, and (4) assaying carbon sources in media that had supported portions of the mycelium which contained developing perithecia, and portions, both inhibited and uninhibited, which contained no developing perithecia. Different kinds and volumes of media and various intervals of time between sequential crosses were used to aid in determining limits of perithecial inhibition. Perithecial inhibition was observed to be independent of volatile metabolites and pH, independent of non-volatile metabolites, reversible by addition of nutrients, dependent upon nutrient volume, and correlated with the concentration of the carbon source in the medium. It is proposed that second crosses are inhibited because of a previous lowering of the concentration of nutrients in the medium in second-cross locations, owing to prior demand upon those nutrients by the developing perithecia in first-cross locations. The possibility of an activation signal between first- and second-cross locations is discussed. No inhibitory substance in inhibited locations was detected.Supported in part by a National Science Foundation Traineeship.     

Methods of investigating populations of the take-all fungus (Ophiobolus graminis) in soil

Attempts to isolate Ophiobolus graminis directly from infested soils failed, so host-infection techniques were used to study soil-borne populations of the fungus. Extracting organic debris from soils and grading it by wet sieving through standard meshes concentrated the fungus. Fractions were tested for infectivity either as layers in pots of sand or by packing into short lengths of polyvinyl chloride tubing, through which wheat seedlings were grown. Coarse debris (retained by 420 μ aperture sieves) was most infectious and usually caused lesions within 3 weeks; whole soil and especially fine debris (< 420 μ) caused fewer and less severe infections, which often became apparent only after 3 weeks. Slight infectivity of the sediment fractions was attributed to imperfect separation of debris. Soil sampled in crop or stubble rows caused more infections than soil from between rows. Usually seedling infection was made manifest by root lesions and runner hyphae, but these symptoms were not always plain or conclusive. Many seedling roots that rotted when kept moist and in the light produced perithecia within 6 weeks. Although perithecia formed on some roots where neither lesions nor hyphae were found, they did not form on all diseased roots. More needs to be known about the factors influencing perithecial formation before it can be used as a reliable confirmatory test.     

Relations entre production et localisation de mycosporine et morphogenèses reproductrices chez le Pyrénomycète Gnomonia leptostyla

Relations between production and localisation of mycosporin and reproductive morphogenesis in the Pyrenomycete Gnomonia leptostyla.
The production of mycosporin (P310) has been analysed in Gnomonia leptostyla (FT.) Ces. et de Not. during mycelial growth and reproductive morphogenesis (macroconidiogenesis, microconidiogenesis and differentiation of perithecia). Conidiogenesis is induced in illuminated cultures while darkness promotes perithecial development. At 20°C, the cultures produce either macroconidia or perithecia with abortive sporophyte. Microconidia differentiation and perithecia maturation require low temperature (10°C). Mycosporin is, at all times, present in the thallus. However, the concentration of mycosporin in highest in the conidiogenous thallus, intermediate in the perithecial thallus. and lowest in the vegetative mycelium. In the conidiogenous thallus, macroconidia and microconidia are both sites of mycosporin accumulation. On the contrary, in the perithecial thallus, mycosporin levels are not higher in perithecia than in mycelia, even during their maturation period. The quantitative variations of mycosporin during the thallus development and its accumulation inside conidia suggest translocation from sites of synthesis towards reproductive cells.     

Experiments using sterilized apple-leaf discs to study the mode of action of urea in suppressing perithecia of Venturia inaequalis (Cke.) Wint.

Laboratory experiments using sterilized apple-leaf discs showed that treatment of leaves with urea during the early stages of perithecial initiation induced a high nitrogen content of the leaves, which prevented further development of perithecia although mycelial growth was unaffected. Treatments applied at a later stage of fungal development inhibited both perithecial and mycelial growth. Some of the bacteria isolated from urea-treated leaves in the field restricted perithecial development, particularly when applied in the first month after inoculation with suspensions of conidia from sexually compatible strains of the fungus. One isolate, a Pseudomonas sp., was shown to be important in the decomposition of apple leaves.     

彩绒革盖菌超微结构的研究

利用电子显微镜对彩绒革盖菌[Coriolus versicolor(L.:Fr.)Quél.],俗名云芝的人工培养的菌丝和野生的子实体进行超微结构的研究。结果表明:子实体由三种类型的菌丝(生殖菌丝、骨架菌丝、联络菌丝)组成。菌丝和子实体菌丝的细胞壁由两层结构组成。担子和担孢子的细胞壁由多层结构组成,至少有三层。菌丝顶端细胞的细胞质中有顶泡复合体(AVC)和顶体。菌丝细胞和子实体菌丝细胞都有桶状隔膜,在细胞质中有丰富的糖原贮存。担孢子与担子的小梗连接处出现初生壁溶化现象。     

Effect of Trichoderma harzianum on perithecial production of Gibberella zeae on wheat straw

Conidial suspensions and cell-free filtrates of Trichoderma harzianum isolates were evaluated for their effectiveness in reducing perithecial and ascospore production of Gibberella zeae on wheat straw. Isolate T-22, which is registered in the US as a biological control agent (Plant Shield™), was included in the study as a positive control. When co-inoculated with G. zeae all 11 isolates of T. harzianum significantly reduced perithecial numbers on wheat straw. Five T. harzianum isolates, including T-22, reduced perithecial formation by 70% or greater. All isolates of G. zeae, varied in their ability to produce perithecia. Isolate 192132 produced the greatest number of perithecia and was used to further evaluate the effect of application time of the T. harzianum isolates. Perithecial reduction was highest (96-99%) when T. harzianum conidial suspension or cell-free filtrate was applied to straw 24 h prior to inoculation with G. zeae. Control was less effective when T. harzianum was applied at the same time (co-inoculated) or 24 h after G. zeae. Treatments which reduced perithecial numbers also reduced ascospore numbers; however, the average numbers of ascospores per perithecia were not significantly lowered. Field trials showed significant reduction of perithecia on residues treated with T. harzianum prior to placement on the soil surface. Both T. harzianum and G. zeae were re-isolated from residues sampled in July and August after 30 and 60 days of exposure to the environment.     

Scanning electron microscopy observations of the interaction between Trichoderma harzianum and perithecia of Gibberella zeae

Chronological events associated with the interaction between a strain of Trichoderma harzianum, T472, with known biological control activity against perithecial production of G. zeae, were studied with scanning electron microscopy to investigate the mechanisms of control. Large clusters of perithecia consisting of 5-15 perithecia formed on the autoclaved, mulched wheat straw inoculated with G. zeae alone (control) with an average of 157 perithecia per plate. Small clusters consisting of 3-6 and an average of 15 perithecia per plate perithecia formed on straw that was treated with T. harzianum. The mature perithecia from straw treated with T. harzianum produced less pigment and were lighter in color than those from the control plates. Furthermore the cells of the outer wall of these perithecia were abnormal in appearance and unevenly distributed across the surface. Immature perithecia were colonized by T. harzianum approximately 15 d after inoculation (dai) with the biocontrol agent and pathogen. Few perithecia were colonized at later stages. The affected perithecia collapsed 21 dai, compared to the perithecia in the control samples that began to collapse 28 dai. Abundant mycelium of T. harzianum was seen on the perithecia of treated samples. Perithecial structures may be resistant to penetration by the mycelium because direct penetration was not observed. Trichoderma harzianum colonized the substrate quickly and out-competed the pathogen, G. zeae.     

Changes of the cytoplasmic ultrastructure during development of sclerotia in Claviceps purpurea (Fr.) Tul.

The development of sclerotia of Claviceps purpurea was investigated by light and electron microscopy. During the first days after infection sterigma and conidiospores are formed. The spores show a moderately developed vacuolar system, they are thick walled and contain about 20% lipid (related to the cell volume) embedded in glycogen. The sterigma are cylindrical unicellular hyphae with electron dense cytoplasm and isolated strongly contrasted lipid droplets. In maturing sclerotia the hyphae become septated with increasingly thick cell walls and a large lipid content. The lipid forms small droplets in young cells, while in the mature sclerotium it occurs in the form of very large drops, occupying the major part of the cell. Simultaneously the composition of the lipid is changed. The mature cells have several nuclei. They are partially connected by osmiophilic substances, forming a network of intercellular spaces.Abbreviations HEPES N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid - DMSO Dimethylsulfoxide