The genus Pilidiella, including its teleomorphs in Schizoparme, has a cosmopolitan distribution and is associated with disease symptoms on many plants. In the past, conidial pigmentation has been used as a character to separate Pilidiella (hyaline to pale brown conidia) from Coniella (dark brown conidia). In recent years, however, the two genera have been regarded as synonymous, the older name Coniella having priority. To address the generic question, sequences of the internal transcribed spacer region (ITS1, ITS2), 5.8S gene, large subunit (LSU) and elongation factor 1-α gene (EF 1-α) were analysed to compare the type species of Pilidiella and Coniella. All three gene regions supported the separation of Coniella from Pilidiella, with the majority of taxa residing in Pilidiella. Pilidiella is characterised by having species with hyaline to pale brown conidia (avg. length[ratio ]width >1.5), in contrast to the dark brown conidia of Coniella (avg. length[ratio ]width [les ]1.5). Pilidiella diplodiella, which is a pathogen associated with white rot of grapevines, was shown to be an older name for C. petrakii. To delineate species in the P. diplodiella species complex, isolates were also compared based on histone (H3) gene sequences. Analyses derived from these sequence data separated P. diplodiella from a newly described species, P. diplodiopsis. The new species P. eucalyptorum sp. nov. is proposed for isolates formerly treated as C. fragariae and associated with leaf spots of Eucalyptus spp. This species clustered basal to Pilidiella, and may represent yet a third genus within this complex. Pilidiella destruens sp. nov. is newly described as anamorph of Schizoparme destruens, which is associated with twig dieback of Eucalyptus spp. in Hawaii. A key based on morphological characteristics is provided to separate the taxa treated in this study.

Geosmithia putterillii is an anamorphic fungus with connections to bark beetles. Genetic variability of 89 isolates traditionally grouped in G. putterillii and G. lavendula isolated from different geographical regions from subcorticolous insects and from other unspecific substrata was assessed using RAPD, sequencing of the ITS region (ITS1-5.8SrDNA-ITS2) and morphological characters. RAPD analysis revealed eight distinct groups. One group was represented by G. lavendula type strain and showed no relations to any other isolate. Five RAPD-types with similar ITS sequences and phenotype were related to the ex-type strain of Penicillium pallidum (generally given as a synonym of G. putterillii). Because of unique phylogenetic position and a phenotype markedly different from G. putterillii, the new combination G. pallida is made here. For another group of isolates formerly identified as G. putterillii the new species G. flava is described based on a characteristic RAPD-type, a unique ITS sequences and a different phenotype. These newly recognized species are stable in culture and with worldwide distribution.

An evaluation was made of the genotypic diversity (DNA fingerprinting) of 269 A. flavus strains, including subpopulations isolated from grain sampled at harvest (91 unique ‘fingerprints’ or genotypes/128 strains), field soil (26 genotypes/31 strains), maize insects (49 genotypes/52 strains) and air-spora (56 genotypes/58 strains), from a maize field near Kilbourne, Illinois. Eight A. flavus genotypes were isolated from grain samples harvested in different years (1988–1991). Genotype 36, isolated from three maize samples, matched the DNA fingerprint of a K. E. Papa strain NRRL 19997, isolated from maize grown in Georgia. Ninety-eight percent of the A. flavus genotypes produced sclerotia and 53% produced aflatoxin. Contrasts of DNA fingerprints revealed two matches involving subpopulations from grain and soil, one match for grain and maize insects, and no matches for grain and air-spora. The high genotypic diversity recorded for each subpopulation, in addition to a limited sample size, precluded any assessment of the relative importance of these subpopulations as sources of A. flavus infective inoculum. Aspergillus parasiticus was routinely isolated from soil samples.

The status of anaerobic zoosporic (Chytridiomycota) fungi along the entire digestive tract of sheep was assessed both analytically and microscopically. Digest samples were taken from different segments of the digestive tracts of three newly killed sheep that previously had been used in experimental dietary studies. These digest samples were tested for the presence of rumen fungi by assessing the recovery of live fungi from the samples, direct observation of digested plant remains under the scanning electron microscope (SEM), and using a chitin assay as an estimation of fungal biomass. Live anaerobic fungi were recovered from the abomasum, small and large intestine, caecum and faeces of sheep, but not from the digest samples of rumen and omasum. However, SEM examination of the samples confirmed the presence of fungal structures from all of these organs. In the large intestine and caecum samples the observed sporangial structures were rounded and showed conspicuous surface pitting. Results of the chitin assay indicated that the anaerobic fungi might account for up to 20% of the total microbial biomass in the rumen of sheep. The results of this study support the view that anaerobic fungi may be present as a resistant stage in the lower reaches of the digestive tract.

The morphology of infection structure development of Puccinia recondita f. sp. tritici on and in susceptible and resistant wheat lines inoculated with urediospores was examined by SEM. The germ-tube extends over the leaf surface and elongates perpendicularly to the long axis of the leaf. When the germ-tube encounters the stomatal lip, an appressorium forms over the stoma and the pore is entered by an infection peg produced on the surface of the appressorium in contact with the host leaf. At 6 h post-inoculation (hpi), infection pegs develop terminally substomatal vesicles (SSVs) in the substomatal chambers of all wheat lines. A septum separates each SSV from its interconnective tube. A primary infection hypha forms terminally from the elongated SSV either parallel to the long axis of the stomatal slit or perpendicular to the leaf surface. When a primary infection hypha attaches to a host cell, a septum forms cutting off the tip of the hypha, delimiting a terminal haustorium mother cell (HMC) by 12 hpi. Secondary infection hyphae arise from a position proximal to, and in the proximity of, the HMC septum. Additional HMCs are formed when a secondary hypha or a tertiary hypha adheres to a plant cell. Infection sites with HMCs were observed at 24 hpi and at subsequent sampling stages. There were no significant differences between the infection processes on the three wheat lines examined in this study.

Species within the genus Botryosphaeria include some of the most widespread and important pathogens of woody plants, and have been the focus of numerous taxonomic studies in recent years. It is currently accepted that anamorphs of Botryosphaeria belong to two distinct genera, Fusicoccum and Diplodia. Species within the genus Fusicoccum commonly produce aseptate, hyaline conidia. In the present study, fungi were isolated from foliage and wood of Eucalyptus in native forests and plantations in Australia. Although these fungi produced Dichomera anamorphs in culture, they clustered within the Fusicoccum clade of Botryosphaeria based on their ITS sequence data. Four species, Botryosphaeria dothidea, B. parva, B. ribis and B. australis produced Dichomera conidia in culture. The Dichomera synanamorphs are described for these four species of Botryosphaeria. In addition, falling within the Fusicoccum clade of Botryosphaeria, two species were found to be distinct from previously described Botryosphaeria spp. based on their ITS sequences, but synonymous with D. versiformis and D. eucalypti. These observations are currently unique to isolates from host trees within the genus Eucalyptus in Australia, and the pleoanamorphic nature of these species is discussed.

The phylogeny of the Dothideomycetes was investigated using nucleotide sequences of SSU and LSU rDNA. 32 new sequences of these regions from 18 species were aligned with five sequences obtained from GenBank, including two representatives of Pezizomycetes used as outgroup. A combined data set of SSU and LSU rDNA was analysed phylogenetically using neighbour-joining and maximum likelihood. The pseudoparaphysate taxa (Pleosporales incl. Melanommatales) form a monophyletic group. A separation of Melanommatales can be rejected using parametric bootstrapping, and this supports previous results obtained from SSU rDNA studies. The aparaphysate Dothideomycetes form a sister-group to the Pleosporales, but with low bootstrap support. Within these species, two well-supported groups can be distinguished, the Dothideales s. str. and the Capnodiales with Myriangiales as sister-groups. The Myriangiales appear paraphyletic, but this has only poor bootstrap support. A monophyly of Dothideales comprising Capnodiales can be rejected with parametric bootstrapping as well as a subdivision of the loculoascomycetes based on form and opening of the ascomata and ascus. The phylogeny of the aparaphysate taxa requires further studies.

All available publications providing descriptions of ectomycorrhizas (ECM) were reviewed in order to build a database containing details on fungus forming the ECM, host tree, country where the material for description was collected, and habitat of the ECM. Other secondary data were also recorded. In all 1244 descriptions of ECM published since 1961 in 479 papers were reviewed. The number of different ECM morphotypes described was 814. Most ECM described were collected in Europe and North America. Gymnosperms were the most common tree associates, and boreal and temperate forests the most studied ecosystems. Fungal symbionts were mostly Basidiomycota, epigeous, and with mushroom-like morphology. The paper also addresses the gaps in ECM knowledge that mycorrhizologists should address in future studies.

Genotypic variation among 62 strains of Aphanomyces euteiches, four of A. cochlioides, and a Saprolegnia sp. was investigated using RAPD analysis. Pathogenicity assays on pea, bean, alfalfa, red clover, and sugarbeet were used to determine host preference among the strains of A. euteiches and A. cochlioides. Pathogenicity tests revealed six pathotypes of A. euteiches with host preferences for bean, alfalfa, pea, pea and alfalfa, red clover and alfalfa, and bean and alfalfa. Another group of strains was non-pathogenic on the five plant species. The host of origin tended to be the host on which each strain incited the highest disease severity. A. euteiches did not incite root rot symptoms on sugarbeet, and A. cochlioides was pathogenic only to sugarbeet. RAPD analyses provided a measure of genetic diversity in Aphanomyces. Fifty random decanucleotide primers were screened with five test strains from four hosts representing different pathotypes, and 32 primers amplified DNA fragments from all five strains. Eight primers were chosen for most of this study based on number and polymorphic nature of the bands generated. RAPD assays of 62 strains of A. euteiches with the eight primers yielded 159 polymorphic and no monomorphic, strongly amplified bands. Cluster analyses of RAPD data revealed genotypic differences among three groups of A. euteiches which corresponded to their host of origin and host preference for bean, alfalfa, and red clover/alfalfa. Strains nonpathogenic on all plants tested formed another genotypic group, corroborating results from the pathogenicity assays that indicated this is a discrete group. The bean and non-pathogenic groups were the most distinct. The A. cochlioides and Saprolegnia strains were genotypically distinct from the pathogenic, but not the non-pathogenic strains of A. euteiches. Reproducibility of RAPD assays was confirmed by replicated amplifications and DNA hybridization analysis. Results indicated that A. euteiches is composed of distinct subspecific groups based on genotype and host preference.

Mycosphaerella punctiformis, the type species of the genus Mycosphaerella, is epitypified by material collected on Quercus robur in The Netherlands. The teleomorph is described in planta, and the Ramularia anamorph, for which the new name R. endophylla is proposed, and the Asteromella spermatial state are characterized in vitro. Sequence data of the nuclear ribosomal DNA are presented and analyzed together with other Mycosphaerella spp. with Ramularia and several other anamorphs. Several strains originating from Quercus, Acer and Tilia showed diverging ITS sequences, indicating that the M. punctiformis complex may comprise more than a single phylogenetic species, but this could not be confirmed by the analysis of our dataset. An endophytic phase is established for the first time in the life-cycle of M. punctiformis, as the species was repeatedly isolated from surface sterilized green healthy leaves of Quercus robur in summer at the epitype locality.

Rhynchosporium secalis causes an economically important foliar disease of barley, rye, and other grasses known as leaf blotch or scald. This species has been difficult to classify due to a paucity of morphological features; the genus Rhynchosporium produces conidia from vegetative hyphae directly, without conidiophores or other structures. Furthermore, no teleomorph has been associated with R. secalis, so essentially nothing is known about its phylogenetic relationships. To identify other fungi that might be related to R. secalis, the 18S ribosomal RNA gene and the internal transcribed spacer (ITS) region (ITS1, 5.8S rRNA gene, and ITS2) were sequenced and compared to those in databases. Among 31 18S sequences downloaded from GenBank, the closest relatives to R. secalis were two species of Graphium (hyphomycetes) and two other accessions that were not identified to genus or species. Therefore, 18S sequences were not useful for elucidating the phylogenetic relationships of R. secalis. However, analyses of 76 ITS sequences revealed very close relationships among R. secalis and species of the discomycete genera Tapesia and Pyrenopeziza, as well as several anamorphic fungi including soybean and Adzuki-bean isolates of Phialophora gregata. These species all clustered together with 100% bootstrap support. On the basis of these results, the teleomorph of R. secalis, if it exists, most likely will be a small apothecium produced directly on dead, infected host tissue. The ITS analysis also indicated that higher-level classifications within the discomycetes need to be revised, and that Tapesia and Pyrenopeziza probably do not belong in the Dermateaceae.

Fungal cultures isolated from oil-polluted sea water near Mumbai, India have been studied for their capability to degrade crude oil. A yeast isolate identified as Yarrowia lipolytica was further investigated with respect to its dimorphic behaviour and alkane degradation. Y. lipolytica NCIM 3589 in the yeast form degraded the aliphatic fraction of crude oil and also pure alkanes (20–60% within 48 h) under aerobic conditions. Unlike most Y. lipolytica strains, our isolate required partial anaerobiosis for mycelium formation. Studies with two isolates suggested that mycelium to yeast transition may be the prerequisite for effective alkane degradation.

Amplified Fragment Length Polymorphism (AFLP) analysis has been used to analyse 100 Australian, European and North American isolates of Leptosphaeria maculans. All isolates had distinct AFLP profiles. They could be classified into five types, which had very few AFLP bands in common and corresponded to classifications made previously on the basis of ability to cause stem cankers on Brassica napus (A group), or inability to do so (B group), and on host range. Four isolates had AFLP profiles completely dissimilar to these groups and to each other. Genetic diversity and geographic differentiation were analysed separately within AFLP types 1 and 2. UPGMA analysis of the 66 AFLP type 1 (A group) isolates using 50 polymorphic bands did not provide evidence for clustering according to geographic origin. Non-metric multidimensional scaling (NMDS) analysis suggested that the Australian and European populations were separate adjacent clusters, while the North American population partially overlapped both the others. This geographic differentiation was supported by Wright's fixation index (Fst) analysis. Three measures of genetic variability between isolates within regions (effective number of alleles, gene diversity, and Shannon index) showed that the North American A group isolates were less diverse than those from Australia and Europe. The 21 AFLP type 2 (B group; NA1 sub-group) isolates did not cluster based on geographic region, which was confirmed by NMDS and Fst analysis. There was a similar degree of genetic diversity within A group and the NA1 sub-group of B group isolates. Unlike other techniques, AFLP analysis can readily discriminate between group B isolates of the L. maculans complex that were previously difficult to classify and also provides individual fingerprints for isolates. Isolates of the A group and of the NA1 sub-group of B group could be also distinguished readily by electrophoretic karyotyping, as the latter isolates had more bands smaller than 1.4 Mb than the A group isolates.

Of the two potato glycoalkaloids, α-chaconine and α-solanine, α-chaconine was the more inhibitory on spore germination in Alternaria brassicicola and Phoma medicaginis, and on growth in liquid culture of these species and also Ascobolus crenulatus and Rhizoctonia solani. At 50 μM or less, solanine caused little (<20%) or no inhibition but, in combination with comparable concentrations of chaconine (which were sometimes also below the activity threshold), synergistic inhibitory effects (up to 100% inhibition) were apparent. A scanning electron microscopic examination of agar-grown cultures of P. medicaginis revealed that both glycoalkaloids at 100 μM inhibited hyphal extension, but that chaconine particularly increased branch formation (three-fold) as well as hyphal thickness and ‘beading’. Glycoalkaloid-containing liquid medium from R. solani cultures did not contain glycoalkaloid hydrolysis products. There was a 17% reduction in the solanine content of the medium, but the chaconine level was not significantly different from that in uninoculated controls. Neither glycoalkaloids nor their hydrolysis products were detectable in the washed mycelium of such cultures.

The genetic structure of three newly established Cryphonectria parasitica populations (Choëx, Weggis, Murg) was analysed and compared to an older, post-epidemic population (Claro). Vegetative compatibility (vc) type and DNA fingerprint analysis revealed an almost clonal C. parasitica population in Choëx, Weggis and Murg. These stands are all situated in northern Switzerland, outside the main range of European chestnut. Only one vc type and one dominant DNA fingerprint was found in Choëx and Murg. In Weggis, two vc types and two dominating DNA fingerprints were found. The European Cryphonectria hypovirus (CHV1) was not detected in these three populations. In contrast, the population in Claro, situated within the main range of European chestnut in southern Switzerland, had much higher vc type and DNA fingerprint diversity. DNA fingerprints were correlated to vc types in Claro and in Weggis. Mating type determination revealed one strongly dominating mating type in each of the three northern populations, but not in Claro. From these results we conclude that C. parasitica disseminated almost exclusively by means of asexual reproduction in Choëx, Weggis and Murg, whereas in Claro sexual reproduction also played an important role. Additionally, founder effects and restricted gene flow were dominating factors in shaping the genetic structure of the three northern populations.

A new ascomycete, Antarctomyces psychrotrophicus gen. et sp. nov., characterised by naked asci, hyaline, thick-walled, ellipsoidal to fusiform, echinulate ascospores, and blastoconidia, isolated from Antarctican soil samples, is described and illustrated. Analysis of the nuclear rDNA ITS region sequences showed that this taxon is related to Thelebolaceae.

Samples of standing senescent culms of Panicum maximum, Pennisetum purpureum, Phragmites australis, Miscanthus floridulus, Saccharum arundinaceum and Thysanolaena maxima (Gramineae), and Schoenoplectus litoralis (Cyperaceae) were collected in Hong Kong between 1997 to 1999. A total of 205 fungal taxa were identified on these samples, including 61 ascomycetes, and 144 mitosporic taxa. Common fungal genera included Diaporthe, Leptosphaeria, Massarina, Ophiobolus and Ophioceras (ascomycetes), and Monodictys, Phaeoisaria, Periconia, Phoma, Phomopsis, Rhinocladiella, Septoria and Sporidesmium (mitosporic taxa). Different grass species were host to different fungal communities and diversities of taxa. Diversity indices for fungi on the hosts varied from 3·3 to 8·7, the highest index being from Pennisetum purpureum, and were overall higher from species offering more durable, strongly sclerenchymatic substrates. No single saprobic fungus collected in this study is thought to be specific to any one grass, however, certain fungi tended to reoccur on single grass species, but not on adjacent grasses. A ‘core fungal group’ was commonly associated with the decaying grasses and this ‘core’ was thought to be important in nutrient cycling in the grasses. A comparison of the fungi occurring on grasses with those on other monocotyledonous hosts is made. The numbers of fungi known to occur on Juncus roemerianus and Phragmites australis are briefly summarised.

A Phytophthora species was found on blighted foliage of Ipomoea longipedunculata, a morning glory native to the highlands of central Mexico. Based on host range, morphology, allozymes, mitochondrial DNA haplotype and rDNA sequences it is concluded that a new Phytophthora species, P. ipomoeae sp. nov., is the causal agent of leaf blight disease on I. longipedunculata.

Diversity in trichothecene mycotoxin production by 167 isolates of Fusarium graminearum was examined by chemical and molecular methods. Isolates from barley, corn, and wheat grown in Korea produced either deoxynivalenol (DON) or nivalenol (NIV), whereas isolates from corn grown in the United States produced DON only. Southern blotting of MseI-digested genomic DNA's from these isolates was performed using a 0.6-kb fragment of Tri5, a key enzyme for trichothecene production, as a probe. This technique revealed a single-band polymorphism between these isolates, with 1.8- and 2.2-kb bands arising from DON and NIV producers, respectively. The same set of isolates was subjected to previously developed PCR assays using primers derived from Tri7 or Tri13. These assays also revealed a single-band polymorphism between NIV- and DON-producing chemotypes. The polymorphisms at Tri5, Tri7, or Tri13 in all of the US isolates were consistent with their chemotypes as identified by GC–MS. However, for seven Korean isolates, chemical and molecular analyses yielded seemingly inconsistent results. This issue was resolved by Southern blot analysis with the Tri5 probe using two other restriction enzymes and sequence comparison of a 3.8-kb region spanning Tri5. In addition, one of these exceptional isolates was found to carry both DON and NIV chemotype-specific regions, possibly resulting from recombination between the two chemotypes.

Net blotch caused by Pyrenophora teres is a serious disease of barley in many cereal production areas world-wide, including the Western Cape province of South Africa. The pathogen occurs as two forms, P. teres f. teres, which produces net-blotch symptoms, and P. teres f. maculata which produces leaf spots. Pyrenophora japonica and P. hordei, which have also been reported in South Africa, also produce spots on susceptible barley cultivars. Using RAPD markers, spot-forming isolates from the South African population were found to be relatively uniform. Single ascospores were obtained from pseudothecia after in vitro mating had occurred between a verified P. teres net-blotch isolate from Denmark and a representative Pyrenophora leaf spot isolate from South Africa. Using amplified fragment length polymorphism (AFLP) and RAPD markers, recombination was demonstrated in the progeny which had DNA banding patterns different from the two parental isolates. Pathogenicity trials also confirmed that recombination had taken place during mating. Inoculations were conducted on differential cultivars susceptible to the net-blotch or leaf spot forms. The two parents induced typical net-blotch or leaf spot symptoms whereas the progeny mostly induced a jagged spot symptom on each cultivar. Fungicide sensitivity tests using the ergosterol biosynthesis inhibitors triademinol, bromuconazole and triticonazole showed that, due to recombination, some progeny could have increased resistance to these fungicides. Due to mating and subsequent recombination between a net blotch isolate of P. teres and a representative leaf spot isolate, it was concluded that the latter was P. teres f. maculata. These results contrast with the earlier belief that Pyrenophora leaf spot isolates in the Western Cape are P. japonica and P. hordei.