This issue of Mycological Research News features: In this issue; The coronomycin producer: a case of mistaken identity?; Long-range self-organization in Dictyostelium; and Resistance variation in natural pathosystems.

Thirteen research papers are included in this part, seven concerning the phylogenetic relationships of plant pathogens: a new invasive Phytophthora on trees, variation and mating systems in P. ramorum, the status of the Microdochium nivale varieties, the position of Pseudocercospora cladosporioides on olives, Verticillium s. lat., an ancestral powdery mildew, and a consideration of Sawadaea spp. along with their maple hosts. Other papers report on parthensomes in corticioid fungi, collembola grazing, the cultivation of Cordyceps unilateralis, genetic diversity in Entomophaga maimaiga, the gold content of macromycetes, and a fossil Aspergillus species from Tertiary amber.

The following new scientific names are introduced: Caespitotheca gen. nov.; Aspergillus collembolorum, and Phytophthora kernoviae spp. nov.; and C. forestalis (syn. Uncinula forestalis), and Microdochium majus (syn. Fusarium nivale var. majus) combs. nov.

A new Phytophthora pathogen of trees and shrubs, previously informally designated Phytophthora taxon C, is formally named here as P. kernoviae. P. kernoviae was discovered in late 2003 during surveys of woodlands in Cornwall, south-west England, for the presence of another invasive pathogen, P. ramorum. P. kernoviae is self-fertile (homothallic), having plerotic oogonia, often with distinctly tapered stalks and amphigynous antheridia. It produces papillate sporangia, sometimes markedly asymmetric with medium length pedicels. Its optimum temperature for growth is ca 18 °C and upper limit ca 26 °. Currently, P. kernoviae is especially noted for causing bleeding stem lesions on mature Fagus sylvatica and foliar and stem necrosis of Rhododendron ponticum. P. kernoviae is the latest of several invasive tree Phytophthoras recently identified in the UK. Its geographical origins and the possible plant health risk it poses are discussed.

Vegetative growth rate, and size of sporangia, chlamydospores and oospores from 94 P. ramorum isolates were measured and the isolates were paired in vitro with four different heterothallic Phytophthora species isolated from infected nursery plants in Germany. P. ramorum isolates originated from different European countries and from Canada and the USA. 66 of the 67 European isolates were determined as mating type A1; only one isolate was of mating type A2. Of the 27 North American isolates tested, seven (all from nurseries) were determined to be the A1 mating type and 17 to be the A2 mating type. Three isolates did not produce gametangia during the incubation period. Discriminant analysis of all data allowed a grouping based on the vegetative growth rate. The two groups corresponded with the mating type no matter whether the isolates originated from Europe or North America. The A1 isolates were much more homogeneous in their morphology than the A2 isolates. They grew faster, had larger chlamydospores and did not produce gametangia with P. cambivora. Within the A2 group, the single European isolate of mating type A2 (BBA 16/02) and three US isolates showed intermediate characters and were classified with the discriminant function into that of the opposite mating type. The morphological characters and the mating behaviour of the isolates will be discussed.

Degenerate PCR primers were designed based on EF-1 alpha (EF-1α) gene sequences of several filamentous fungi retrieved from sequence databases. These primers were used to isolate a partial sequence, approximately 830 bp in length of the EF-1α from isolates of Microdochium nivale obtained from various geographic locations across the world. Two distinct groups of isolates were evident among those isolates examined. Sequence homology for comparisons within group was 99.7% for group A and 99.8% for group B. Primers specific to either group A or group B sequences were designed and tested on isolates from around the world. Comparisons were made with primers previously reported for the two varieties of M. nivale and revealed that Group A type isolates correlated with M. nivale var. majus and group B isolates with M. nivale var. nivale.

The primers from this study and those previously reported were in agreement for all isolates with the exception of one isolate (NRRL 3289) which failed to amplify with previously published M. nivale primers. Sequence analysis of NRRL 3289 suggested that it was an isolate of M. nivale var. nivale as indicated by the EF-1α based primers developed in this study. This study provides sequence based phylogenetic evidence of two species and when taken together with biological differences reported, leads to the recognition of M. majus comb. nov. (syn. Fusarium nivale var. majus). Descriptions of the two species are provided.

Cercospora leaf spot of olives is a serious defoliating disease attributed to Pseudocercospora cladosporioides. Although the disease is well distributed throughout olive growing regions of the world, its epidemiology and population structure remains unknown. The aim of this study was to establish the genetic variability of Spanish isolates of P. cladosporioides using DNA sequence data from the ITS region, as well as two protein-coding genes, actin and calmodulin. Phylogenetic data obtained here support P. cladosporioides as closely related to other Pseudocercospora species that cluster within Mycosphaerella. Spanish isolates clustered in two clades: isolates from Catalonia were different from those collected in Andalusia. However, isolates appeared to be genetically relatively homogeneous, suggesting that chemical control of this disease via a managed spraying programme may prove a viable option for controlling the disease in Spain.

21 strains with all typical morphological characteristics of eight Verticillium species (Phyllachorales) were studied in this work, together with representatives from four Hypocreales species (11 strains), that were previously classified as members of the genus. The PCR products from two nuclear genes, i.e. the ITS1-5.8S-ITS2 region and RNA polymerase II largest subunit gene (rpb1), together with four mitochondrial genes, i.e. the small ribosomal rRNA subunit (rns), the two NADH dehydrogenase subunit genes (nad1 and nad3), and the cytochrome oxidase subunit III gene (cox3) were sequenced and analyzed. Similarly, antibodies raised against one strain of each of the species examined (V. nubilum and V. theobromae excluded) were used against the proteins of all other strains. The number and relative area of precipitates formed after crossed electrophoreses served to estimate the degree of immunochemical relatedness. Combined molecular and immunochemical data clarified the phylogenetic relationships of all true Verticillium species and provided a convincing insight into the evolutionary relation of the sect. Nigrescentia with members of the sect. Verticillium and sect. Prostrata that until recently were included in Verticillium.

The phylogenetic position of Uncinula forestalis within the Erysiphales has been inferred from 5.8S, 18S, and 28S rDNA sequences. Although the appendages of the ascomata are Uncinula-like, i.e. unbranched with curved-coiled apices, U. forestalis is situated at the very base of the large Erysiphales cluster, far from the ‘Pseudoidium’ clade (Erysiphe, including Microsphaera and Uncinula) and separate from the recently introduced basal genus Parauncinula. U. forestalis differs morphologically from the species of Erysiphe sect. Uncinula in having terminal, fasciculate (as in Podosphaera tridactyla), septate ascoma appendages and a Euoidium-like anamorph (conidia catenate). In Parauncinula, the appendages are also terminal but not fasciculate, the ascospores are curved, and the anamorph is lacking. Uncinula forestalis is a basal, tree-inhabiting powdery mildew with some additional ancestral characteristics, including Uncinula-like appendages and 6–8-spored asci. The new genus Caespitotheca gen. nov. is described with C. forestalis comb. nov. (syn. Uncinula forestalis) as the type species. We calculated the timing of the divergence of U. forestalis and P. septata using a molecular clock of the Erysiphales (6.5×10−10 changes per site per year in domains D1 and D2 of 28S rDNA) and a 28S rDNA data set. The results suggest that the divergence of U. forestalis and P. septata from other Erysiphales occurred between 90 and 80 Myr ago; i.e. the divergence of the two ancestral species may have occurred in the late Cretaceous.

To understand the phylogenetic relationships and evolution of the powdery mildew genus Sawadaea (Ascomycota: Erysiphaceae), obligate parasitic fungi of maples, we performed molecular phylogenetic analyses based on 47 ITS and ten 28S rDNA sequences. Seven major clades of Sawadaea, each represented by powdery mildew specimens collected from a single or a small number of closely related sections of Acer (maples), were identified in this study, suggesting that a close evolutionary relationship exists between Acer (host) and Sawadaea (parasite). A 6–11-base insertion/deletion was found in the ITS1 region of Sawadaea, and the presence or absence of the indel was consistent within the respective clades. Because the outgroup genera Podosphaera and Cystotheca have no deletions in these sites, deletion of the sequences may have occurred during the divergence of the respective clades of Sawadaea. The seven clades of Sawadaea were divided into two geographical groups, viz. an East Asian and a global group, based on the countries of collection. Calculation of the evolutionary timing of Sawadaea using molecular clocks showed that the divergence of different species of Acer occurred many millions of years before the radiation of Sawadaea. Thus, the close evolutionary relationship between Sawadaea and Acer found in this study might not be due to a true coevolutionary process. Powdery mildew fungi belonging to Sawadaea may have jumped onto Acer spp. long after the radiation of the major sections of these trees, and then expanded their host ranges according to the phylogeny and geographical distribution of Acer.

The parenthesome structure of seven corticioid species, traditionally referred to the family Corticiaceae (Basidiomycota), were studied in order to better understand their taxonomic position: Phanerochaete velutina, Phlebia radiata, P. rufa, Rhizochaete americana (syn. Ceraceomyces americana), R. brunnea, R. filamentosa (syn. Phanerochaete filamentosa) and R. radicata (syn. Phanerochaete radicata). All possessed the perforate type of parenthesome that is commonly encountered in homobasidiomycetes. This feature excludes the above taxa from both the hymenochaetoid and the cantharelloid clades which are the only groups that have imperforate parenthesomes in the homobasidiomycetes.

The effects of grazing by the collembolan Folsomia candida on mycelial foraging patterns of Hypholoma fasciculare growing from beech (Fagus sylvatica) wood block inocula in trays of non-sterile soil was investigated. The wood inocula differed in size, state of decay (time for which wood has been colonized: 2 yr, 1 yr, 6 and 3 months) and nutrient status (inocula colonized on malt agar or nutrient agar). Mycelia were most luxuriant, had greater hyphal coverage and extended more rapidly from 2 yr old than younger inocula, from 4 cm3 than 1 cm3 inocula, and from inocula colonized on malt extract agar rather than on distilled water agar. Grazing dramatically reduced coverage and extension, especially in the less luxuriant systems characterized by many fine hyphae and fewer mycelial cords. Grazing by collembola often resulted in points of more rapid outgrowth as cords with a fanned margin. Results are discussed in terms of fungal foraging strategies.

Cordyceps unilateralis, a fastidious insect pathogenic fungus, was found to produce red naphthoqinones, which possess anti-malarial activity. A method for the isolation and in vitro cultivation of this fungus was, therefore, developed in this study. Ascospores from ant cadavers were used as starting materials, and their secondary spores were allowed to germinate first on PDA for 2 d. Secondary spores were then transferred to Grace's Insect Cell Medium+2 mM glutamine and 10% fetal bovine serum, incubated for 7 d, after which the formation of mycelia was stimulated by transfer to potato dextrose broth. As a result, the growth of C. unilateralis from the steps of secondary spore germination, blastospore formation and mycelial growth was successfully completed for the first time.

Entomophaga maimaiga is a naturally occurring fungal pathogen specific to larvae of the gypsy moth, Lymantria dispar. E. maimaiga is thought to be native to Asia where its epizootics can suppress gypsy moth outbreaks. However, in the USA this beneficial fungal pathogen was not observed until 1989, although an isolate of E. maimaiga from Tokyo was released in Massachusetts to control gypsy moths as early as in 1910–1911, and another isolate from Ishikawa Prefecture in Japan was later released in 1985 and 1986 in New York and Virginia. Our objectives were to: (1) test the hypothesis that E. maimaiga populations in the USA have reduced genetic variability due to founder effects compared to the putative ancestral populations in Asia; (2) track the origin of the North American populations of this fungus; and (3) assess whether genetic differences among E. maimaiga isolates are correlated to morphological differences. We compared genetic diversity among 30 E. maimaiga isolates originating from seven states in the USA, five prefectures in Japan, one province of China and one region of far eastern Russia by AFLPs. Among 14 USA isolates, only ten polymorphic AFLP loci were found, whereas 56 polymorphic loci were found among 16 Asian isolates; 29 loci were polymorphic among 12 isolates from Japan alone. Average gene diversity (h¯) for the polymorphic loci was 0.223±0.005 for Asia (including Japan), 0.131±0.006 for Japan only, and 0.041±0.004 for the USA. Thus, native populations from Asia were more diverse than the USA populations. These results are consistent with the expectation of a population founded from a source population by a small number of individuals. Distance and parsimony analyses of AFLP data showed that the isolates from the USA formed one distinct clade that was most closely related to Japanese isolates collected outside the Tokyo area. No morphological variation of E. maimaiga from different geographical locations was detected.

Ectomycorrhizal and saprobic macrofungi growing in the wild were collected from non-auriferous and unpolluted areas and analyzed for gold. Gold was determined using long-term instrumental neutron activation analysis (INAA). In total, 154 samples, including 67 species of ectomycorrhizal fungi and 22 species of terrestrial saprobes, were examined. Gold contents of the both groups were mostly less than 20 ng g−1 of D.W. The highest concentrations (expressed in D.W.) were found in the ectomycorrhizal species Amanita strobiliformis (136 ng g−1), Russula claroflava (148 ng g−1), Cantharellus lutescens (156 and 210 ng g−1), and Boletus edulis (235 ng g−1). Among the saprobic fungi, the highest values were found in Langermannia gigantea (160 ng g−1) and Morchella esculenta (189 ng g−1). Species of Agaricus commonly had relatively high gold values, 10s of ng g−1. The gold content of macrofungal fruit bodies was considerably higher than that of vascular plants, and parallels concentrations found in plants growing in auriferous areas.

A piece of Baltic amber (Tertiary, Eocene) contains an inclusion of a springtail (Collembola) which is overgrown by an Aspergillus species. The fossil fungus is described as A. collembolorum sp. nov. The excellent mode of preservation of the numerous conidiophores is remarkable and can be explained by sporulation in liquid resin. This is the second report of a fossil Aspergillus, the first being from Dominican amber.