Fungal Diversity最新文献

Ips is a genus of bark beetles found throughout the Northern Hemisphere, many of which are highly destructive to coniferous forests and plantations. Fungal symbionts, especially ophiostomatoid fungi, have contributed to the success of Ips bark beetles. Recently, climate change accelerated tree mortality caused by bark beetles and their fungal symbionts. However, the knowledge of ophiostomatoid fungi associated with Ips bark beetles is inadequate in China. Therefore, this study investigated the ophiostomatoid fungal communities associated with different Ips bark beetles from various coniferous forest areas of China. A total of 14,512 ophiostomatoid fungal strains were isolated from 1265 vigorous adult beetles and 826 fresh galleries belonging to 11 Ips species infesting 16 coniferous tree species, including pines, spruces, and larches, from 42 sampling sites in nine provinces or autonomous regions in northeast, northwest and southwest China. Based on a combination of morphological features and phylogenetic analysis, 71 taxa belonging to eight genera were identified (Ceratocystiopsis, Graphilbum, Grosmannia, Leptographium, Masuyamyces, and Ophiostoma in Ophiostomatales; Endoconidiophora and Graphium in Microascales), of which 38 species were described as new. Comparing patterns of fungal assemblages indicated that fungal symbionts genetically co-differentiated with their vectors. Host trees possibly reinforce the coarse species-specific association between ophiostomatoid fungi and Ips bark beetles. This study further demonstrates the high diversity of ophiostomatoid fungi associated with Ips bark beetles and provides insights into their symbiotic associations.

Hyphomycetes are asexually reproducing parts in a fungal life cycle, and is an artificial classification. Hyphomycetes are fungi with diverse lifestyles, including saprobes, endophytes, plant and animal pathogens, hyperparasites, lichenized forms and extremophiles. Traditionally, morphological characters have been used to identify and classify hyphomycetes, which has led to many taxonomic controversies. Modern molecular methods based on DNA sequence data have developed a more reliable and natural classification of hyphomycetes. The present study revises the taxonomy of the brown-spored hyphomycetes based on both morphology and phylogeny. In total, 1,041 genera with brief notes are provided. Of these, 1,032 genera belong to Ascomycota (Dothideomycetes: 362; Eurotiomycetes: 34; Leotiomycetes: 22; Pezizomycetes: 7; Sordariomycetes: 210; Ascomycota genera incertae sedis: 397), and nine genera belong to Basidiomycota. In addition, 363 brown-spored hyphomycetous genera published since 2010 are listed. Multi-locus phylogeny, including 658 brown-spored hyphomycete genera within Ascomycota, are carried out using 28S nrDNA, 18S nrDNA and RNA polymerase II second largest subunit (rpb2), and the results show that 374 genera are phylogenetically placed in Dothideomycetes, 39 genera in Eurotiomycetes, 26 genera in Leotiomycetes, 6 genera in Pezizomycetes and 213 genera in Sordariomycetes. Based on the morphology and multi-gene phylogeny, 45 fresh collections are described in this study, including seven new genera, viz. Murihylinia, Pseudobrachysporiella, Saprosporodochifer, Solitariconidiophora, Tenebrosynnematica, Xenoberkleasmium, Xenostanjehughesia; 17 new species, viz. Acrodictys thailandica, Alfaria fusiformis, Conioscypha punctiformis, Gamsomyces breve, Murihylinia guizhouensis, Parafuscosporella atricolor, Pleocatenata thailandica, Polyplosphaeria appendiculata, Pseudobrachysporiella pyriforme, Saprosporodochifer fuscus, Solitariconidiophora guizhouensis, Sporidesmiella obovoidispora, Stachybotrys ellipsoidea, Tenebrosynnematica obclavata, Vanakripa obovoidea, Xenoberkleasmium chiangraiense, Yunnanomyces muriformis; one new combination, viz. Xenostanjehughesia polypora; nine new records, viz. Aquatisphaeria thailandica, Bahusandhika indica, Corynespora submersa, Fusariella sinensis, Helicodochium aquaticum, Pleopunctum ellipsoideum, Rhexoacrodictys erecta, Vikalpa dujuanhuensis, Virgaria nigra. Detailed descriptions and morphological illustrations are provided for these new taxa. Current taxonomic difficulties are discussed.

The Microsporidia, an often overlooked fungal lineage, exhibit increasing diversity and taxonomic understanding with the use of genomic techniques. They are obligate parasites infecting a diversity of hosts, including crustaceans. Crustacea are, in essence, ancient insects and their relationship with the Microsporidia is both diverse and convoluted. Relationships between crayfish and their microsporidian parasites display geospatial and taxonomic diversity. Through classical (histological, ultrastructural, developmental) and genomic (phylogenetic, phylogenomic) approaches, we expand the known diversity of crayfish-infecting microsporidia into the genus Nosema by describing three novel species from North America: Nosema astafloridana n. sp. infecting Procambarus pictus and Procambarus spiculifer, Nosema rusticus n. sp. infecting Faxonius rusticus, and Nosema wisconsinii n. sp. infecting Faxonius propinquus and Faxonius virilis. Additionally, we provide SSU sequence data for further Nosema diversity from Procambarus clarkii and Pacifasticus gambelii. The taxonomy of aquatic crustacean-infecting Nosema have been under scrutiny among microsporidiologists—using genomic data we solidify this systematic relationship. Our genomic data reveal phylogenomic divergence between terrestrial insect-infecting Nosema and aquatic crustacean-infecting Nosema but place our novel species within the Nosema. Comparative genomic analysis reveal that Nosema rusticus n. sp. is a tetraploid organism, making this the first known polyploid from the genus Nosema. Annotation of the genomic data highlight that crayfish-infecting Nosema have distinct proteomic differences when compared to amphipod and insect-infecting microsporidians. Alongside the new diversity uncovered and genome-supported systematics, we consider the role of these new ‘invasive’ parasites in biological invasion systems, exploring their relationship with their invasive hosts.

Estimates of global fungal diversity have varied widely, suggesting a range from fewer than one million to over 10 million species, with each of the estimates drawing data from various criteria. In 2022, Fungal Diversity published a special issue on fungal numbers. It had been hoped that the editorial would provide a more accurate account of the numbers of fungi. Instead, it was concluded that this was not possible based on present evidence and, some of the data necessary for accurate assessments was put forward, and the present paper expands on this short article. The review first looks at estimates of fungal numbers and what these estimates are based on. It then presents future research needs that will help us to gain a more accurate estimate of fungal numbers. This includes work that needs to be done in tropical rainforests, where the greatest diversity is expected, where whole rainforests, canopy diversity, and palm fungi are addressed. Case studies for lichens and associated fungi, soil and litter fungi, evidence from particle filtration, freshwater fungi, marine fungi, mushrooms, and yeasts will also be given. Once we have such information, we can obtain a more accurate estimate of fungal numbers.

Fungi are one of the most diverse groups of organisms with an estimated number of species in the range of 2–3 million. The higher-level ranking of fungi has been discussed in the framework of molecular phylogenetics since Hibbett et al., and the definition and the higher ranks (e.g., phyla) of the ‘true fungi’ have been revised in several subsequent publications. Rapid accumulation of novel genomic data and the advancements in phylogenetics now facilitate a robust and precise foundation for the higher-level classification within the kingdom. This study provides an updated classification of the kingdom Fungi, drawing upon a comprehensive phylogenomic analysis of Holomycota, with which we outline well-supported nodes of the fungal tree and explore more contentious groupings. We accept 19 phyla of Fungi, viz. Aphelidiomycota, Ascomycota, Basidiobolomycota, Basidiomycota, Blastocladiomycota, Calcarisporiellomycota, Chytridiomycota, Entomophthoromycota, Entorrhizomycota, Glomeromycota, Kickxellomycota, Monoblepharomycota, Mortierellomycota, Mucoromycota, Neocallimastigomycota, Olpidiomycota, Rozellomycota, Sanchytriomycota, and Zoopagomycota. In the phylogenies, Caulochytriomycota resides in Chytridiomycota; thus, the former is regarded as a synonym of the latter, while Caulochytriomycetes is viewed as a class in Chytridiomycota. We provide a description of each phylum followed by its classes. A new subphylum, Sanchytriomycotina Karpov is introduced as the only subphylum in Sanchytriomycota. The subclass Pneumocystomycetidae Kirk et al. in Pneumocystomycetes, Ascomycota is invalid and thus validated. Placements of fossil fungi in phyla and classes are also discussed, providing examples.

Many taxonomic and systematic rearrangements were proposed to Marasmius Fr. since its original concept in 1835, and since 1980 when it became the type of Marasmiaceae. These were based on morphological and/or more recently molecular phylogenetic studies. This study conducted a comprehensive taxonomic and systematic evaluation of Marasmius that benefits the whole family, implementing multilocus (SSU, LSU, ITS, rpb2 and ef1-α) phylogenetic analyses integrated with morphological and other features. The resulting trees support (1) a Marasmiaceae clade-based circumscription within Marasmiineae, (2) a Marasmius clade-based circumscription within Marasmiaceae, and (3) a subgenus-section-subsection-series system. Two subgenera are proposed: Globulares and Marasmius. Marasmius auton. subgen. includes Crinis-eques sect. nov., sect. Marasmius, Sanguirotales sect. nov., Variabilispori sect. nov., and Sicciformes sect. nov., while Globulares subg. nov. groups sect. Globulares and sect. Sicci. Four subsections are proposed in sect. Globulares and three in sect. Marasmius and sect. Sicciformes. Seventeen series were defined in sect. Globulares and three in sect. Sicci. Selected traits were assessed for their phylogenetic signals within Marasmius, providing a robust framework for a natural system. Based on this analysis, Marasmiaceae includes Chaetocalathus, Crinipellis, Marasmius and Moniliophthora/Paramarasmius, and Campanellaceae fam. nov. includes Brunneocorticium, Campanella/Tetrapyrgos, Neocampanella, and Marasmiellus sect. Candidi. New species, names, combinations and epitypes are also proposed.

Diaporthe is an important plant pathogenic genus, which also occurs as endophytes and saprobes. Many Diaporthe species that are morphologically similar proved to be genetically distinct. The current understanding of Diaporthe taxonomy by applying morphological characters, host associations and multi-gene phylogeny are problematic leading to overestimation/underestimation of species numbers of this significant fungal pathogenic genus. Currently, there are no definite boundaries for the accepted species. Hence, the present study aims to re-structure the genus Diaporthe, based on single gene phylogenies (ITS, tef, tub, cal and his), multi-gene phylogeny justified by applying GCPSR (Genealogical Concordance Phylogenetic Species Recognition) methodology as well as the coalescence-based models (PTP—Poisson Tree Processes and mPTP—multi-rate Poisson Tree Processes). Considering all available type isolates of Diaporthe, the genus is divided into seven sections while boundaries for 13 species and 15 species-complexes are proposed. To support this re-assessment of the genus, 82 Diaporthe isolates obtained from woody hosts in Guizhou Province in China were investigated and revealed the presence of two novel species and 17 previously known species. Synonymies are specified for 31 species based on molecular data and morphological studies. Dividing Diaporthe into several specific sections based on phylogenetic analyses can avoid the construction of lengthy phylogenetic trees of the entire genus in future taxonomic studies. In other words, when one conducts research related to the genus, only species from the appropriate section need to be selected for phylogenetic analysis.