Showing papers in "Fungal Diversity in 2021"
TL;DR: This study shows why the identification of a fungal species is an intricate and laborious task that requires a background in mycology, molecular biological skills, training in molecular evolutionary analysis, and knowledge of taxonomic literature.
Abstract: Modern taxonomy has developed towards the establishment of global authoritative lists of species that assume the standardized principles of species recognition, at least in a given taxonomic group. However, in fungi, species delimitation is frequently subjective because it depends on the choice of a species concept and the criteria selected by a taxonomist. Contrary to it, identification of fungal species is expected to be accurate and precise because it should predict the properties that are required for applications or that are relevant in pathology. The industrial and plant-beneficial fungi from the genus Trichoderma (Hypocreales) offer a suitable model to address this collision between species delimitation and species identification. A few decades ago, Trichoderma diversity was limited to a few dozen species. The introduction of molecular evolutionary methods resulted in the exponential expansion of Trichoderma taxonomy, with up to 50 new species recognized per year. Here, we have reviewed the genus-wide taxonomy of Trichoderma and compiled a complete inventory of all Trichoderma species and DNA barcoding material deposited in public databases (the inventory is available at the website of the International Subcommission on Taxonomy of Trichoderma www.trichoderma.info
). Among the 375 species with valid names as of July 2020, 361 (96%) have been cultivated in vitro and DNA barcoded. Thus, we have developed a protocol for molecular identification of Trichoderma that requires analysis of the three DNA barcodes (ITS, tef1, and rpb2), and it is supported by online tools that are available on www.trichokey.info
. We then used all the whole-genome sequenced (WGS) Trichoderma strains that are available in public databases to provide versatile practical examples of molecular identification, reveal shortcomings, and discuss possible ambiguities. Based on the Trichoderma example, this study shows why the identification of a fungal species is an intricate and laborious task that requires a background in mycology, molecular biological skills, training in molecular evolutionary analysis, and knowledge of taxonomic literature. We provide an in-depth discussion of species concepts that are applied in Trichoderma taxonomy, and conclude that these fungi are particularly suitable for the implementation of a polyphasic approach that was first introduced in Trichoderma taxonomy by John Bissett (1948–2020), whose work inspired the current study. We also propose a regulatory and unifying role of international commissions on the taxonomy of particular fungal groups. An important outcome of this work is the demonstration of an urgent need for cooperation between Trichoderma researchers to get prepared to the efficient use of the upcoming wave of Trichoderma genomic data.
88 citations
TL;DR: It is shown that at a 97% sequence similarity threshold, the total richness of non-singleton fungal taxa across the studies published so far is 1.08 million, representing a conservative estimate of global fungal species richness.
Abstract: High-throughput DNA sequencing has dramatically transformed several areas of biodiversity research including mycology. Despite limitations, high-throughput sequencing is nowadays a predominant method to characterize the alpha and beta diversity of fungal communities. Across the papers utilizing high-throughput sequencing approaches to study natural habitats in terrestrial ecosystems worldwide, > 200 studies published until 2019 have generated over 250 million sequences of the primary mycological metabarcoding marker, the nuclear ribosomal internal transcribed spacer 2 (ITS2). Here we show that at a 97% sequence similarity threshold, the total richness of non-singleton fungal taxa across the studies published so far is 1.08 million, mostly Ascomycota (56.8% of the taxa) and Basidiomycota (36.7% of the taxa). The Chao-1 estimate of the total extant fungal diversity based on this dataset is 6.28 million taxa, representing a conservative estimate of global fungal species richness. Soil and litter represent the habitats with the highest alpha diversity of fungi followed by air, plant shoots, plant roots and deadwood with Chao-1 predictions, for samples containing 5000 sequences, of 1219, 569, 392, 228, 215 and 140 molecular species, respectively. Based on the high-throughput sequencing data, the highest proportion of unknown fungal species is associated with samples of lichen and plant tissues. When considering the use of high-throughput sequencing for the estimation of global fungal diversity, the limitations of the method have to be taken into account, some of which are sequencing platform-specific while others are inherent to the metabarcoding approaches of species representation. In this respect, high-throughput sequencing data can complement fungal diversity predictions based on methods of traditional mycology and increase our understanding of fungal biodiversity.
71 citations
TL;DR: This work provides a comprehensive overview of occurrence data of Colletotrichum species, compiling host range and geographical distribution, with relevance for plant pathology and conservation mycology.
Abstract: The taxonomy of the genus Colletotrichum has undergone tremendous changes over the last decade, with over 200 species being currently recognised and species complexes being informally used to cluster those species. Many of these species are important plant pathogens, some rather polyphagous and others host-specific, but several occur seldomly and some may in fact be ecologically endangered. Based mainly on literature from the past decade, in this work we review the occurrence, geographic distribution and host spectrum of currently recognised Colletotrichum species under phylogenetic, pathological/agronomic and ecological perspectives, providing a list arranged by Colletotrichum species and species complexes. A total of 257 species are listed and grouped into 15 species complexes. In this work we have recorded 1353 unique host species-Colletotrichum species association records from 720 hosts, with the Fabaceae as the family with higher number of hosts (52 host species) but with the Rosaceae as the family with the highest number of host species-Colletotrichum species association records (118 association records). According to occurrence data, 88 species are common in nature, 128 were considered as data deficient and 41 are threatened, some of which are likely extinct from nature and preserved only in culture collections. Several species are relevant plant pathogens, in some cases geographically confined and thus of potential quarantine relevance. Based on the major changes that occurred on Colletotrichum taxonomy over the last decade, this work provides a comprehensive overview of occurrence data of Colletotrichum species, compiling host range and geographical distribution, with relevance for plant pathology and conservation mycology. The current taxonomic framework in Colletotrichum is revealing numerous species but poses challenges to the employment of standard criteria for the evaluation of biological conservation of these fungi. We advocate that conservation mycology and taxonomy should find common routes simultaneously enabling the correct delimitation of species of Colletotrichum and the implementation of feasible criteria for the evaluation of conservation. The employment of new technologies, such whole genome sequencing (WGS), will help and support the description of new species and to gain a better understanding of the genetic bases of speciation processes.
57 citations
TL;DR: It is shown that coalescent approaches and multi-locus phylogeny are crucial to establish species boundaries in Colletotrichum and no single marker could discriminate between species in all complexes.
Abstract: Colletotrichum is one of the most important plant pathogenic genera that is responsible for numerous diseases which can have a profound impact on the agricultural sector. Species delineation is difficult due to a lack of distinctive phenotypic variation. Therefore, in this study three different genomic approaches based on phylogenetic, evolutionary and coalescent-based methods are applied to establish robust species boundaries. The reliability of five different DNA barcodes was also assessed to provide further insights into species delineation. The ITS region can resolve the placement of taxa up to the species complex level. The GAPDH and TUB2 markers are determined to be the most informative for most complexes. However, no single marker could discriminate between species in all complexes, therefore different molecular approaches based on multi-locus datasets are recommended. This is the first study to provide an estimated divergence time for all species complexes in Colletotrichum. The estimated divergence time for species complexes ranged between 4.8 to 32.2 MYA. Based on the high level of congruent results obtained from the different molecular approaches, a new species complex, the Colletotrichum agaves complex is introduced. This complex consists of five taxa which are characterised by the presence of straight or slightly curved conidia with obtuse apices. This study shows that coalescent approaches and multi-locus phylogeny are crucial to establish species boundaries in Colletotrichum. The taxonomic placement of three singleton taxa Colletotrichum axonopodi, C. cariniferi and C. parallelophorum is revised. We accept 248 species and provide recommendations regarding species boundaries in the graminicola–caudatum complex.
56 citations
TL;DR: It is demonstrated that Karst caves encompass a high fungal diversity, including a number of previously unknown species, including one new genus of Cordycipitaceae, Gamszarea, and five new combinations are established.
Abstract: Karst caves are characterized by darkness, low temperature, high humidity, and oligotrophic organisms due to its relatively closed and strongly zonal environments. Up to now, 1626 species in 644 genera of fungi have been reported from caves and mines worldwide. In this study, we investigated the culturable mycobiota in karst caves in southwest China. In total, 251 samples from thirteen caves were collected and 2344 fungal strains were isolated using dilution plate method. Preliminary ITS analyses showed that these strains belonged to 610 species in 253 genera. Among these species, 88.0% belonged to Ascomycota, 8.0% Basidiomycota, 1.9% Mortierellomycota, 1.9% Mucoromycota, and 0.2% Glomeromycota. The majority of these species have been previously known from other environments, and some of them are known as mycorrhizal or pathogenic fungi. About 52.8% of these species were discovered for the first time in karst caves. Based on morphological and phylogenetic distinctions, 33 new species were identified and described in this paper. Meanwhile, one new genus of Cordycipitaceae, Gamszarea, and five new combinations are established. This work further demonstrated that Karst caves encompass a high fungal diversity, including a number of previously unknown species. Taxonomic novelties: New genus: Gamszarea Z.F. Zhang & L. Cai; Novel species: Amphichorda cavernicola, Aspergillus limoniformis, Aspergillus phialiformis, Aspergillus phialosimplex, Auxarthron chinense, Auxarthron guangxiense, Auxarthronopsis globiasca, Auxarthronopsis pedicellaris, Auxarthronopsis pulverea, Auxarthronopsis stercicola, Chrysosporium pallidum, Gamszarea humicola, Gamszarea lunata, Gamszarea microspora, Gymnoascus flavus, Jattaea reniformis, Lecanicillium magnisporum, Microascus collaris, Microascus levis, Microascus sparsimycelialis, Microascus superficialis, Microascus trigonus, Nigrospora globosa, Paracremonium apiculatum, Paracremonium ellipsoideum, Paraphaeosphaeria hydei, Pseudoscopulariopsis asperispora, Setophaeosphaeria microspora, Simplicillium album, Simplicillium humicola, Wardomycopsis dolichi, Wardomycopsis ellipsoconidiophora, Wardomycopsis fusca; New combinations: Gamszarea indonesiaca (Kurihara & Sukarno) Z.F. Zhang & L. Cai, Gamszarea kalimantanensis (Kurihara & Sukarno) Z.F. Zhang & L. Cai, Gamszarea restricta (Hubka, Kubatova, Nonaka, Cmokova & Řehulka) Z.F. Zhang & L. Cai, Gamszarea testudinea (Hubka, Kubatova, Nonaka, Cmokova & Řehulka) Z.F. Zhang & L. Cai, Gamszarea wallacei (H.C. Evans) Z.F. Zhang & L. Cai.
53 citations
TL;DR: The results showed that both species share 95% of their genes corresponding to more than 700 strain-specific proteins, preventing species delimitation based on traditional concepts and providing an important starting point for the establishment of a stable phylogeny of the Xylariales.
Abstract: The Hypoxylaceae (Xylariales, Ascomycota) is a diverse family of mainly saprotrophic fungi, which commonly occur in angiosperm-dominated forests around the world. Despite their importance in forest and plant ecology as well as a prolific source of secondary metabolites and enzymes, genome sequences of related taxa are scarce and usually derived from environmental isolates. To address this lack of knowledge thirteen taxonomically well-defined representatives of the family and one member of the closely related Xylariaceae were genome sequenced using combinations of Illumina and Oxford nanopore technologies or PacBio sequencing. The workflow leads to high quality draft genome sequences with an average N50 of 3.0 Mbp. A backbone phylogenomic tree was calculated based on the amino acid sequences of 4912 core genes reflecting the current accepted taxonomic concept of the Hypoxylaceae. A Percentage of Conserved Proteins (POCP) analysis revealed that 70% of the proteins are conserved within the family, a value with potential application for the definition of family boundaries within the order Xylariales. Also, Hypomontagnella spongiphila is proposed as a new marine derived lineage of Hypom. monticulosa based on in-depth genomic comparison and morphological differences of the cultures. The results showed that both species share 95% of their genes corresponding to more than 700 strain-specific proteins. This difference is not reflected by standard taxonomic assessments (morphology of sexual and asexual morph, chemotaxonomy, phylogeny), preventing species delimitation based on traditional concepts. Genetic changes are likely to be the result of environmental adaptations and selective pressure, the driving force of speciation. These data provide an important starting point for the establishment of a stable phylogeny of the Xylariales; they enable studies on evolution, ecological behavior and biosynthesis of natural products; and they significantly advance the taxonomy of fungi.
52 citations
TL;DR: This review provides a set of guidelines, encouraging an integrative taxonomic approach for species delimitation that can be used to define fungal species boundaries in the future.
Abstract: This is the opening paper in the special issue of Fungal Diversity, which collates the data on defining species. Defining and recognizing species has long been a controversial issue. Since Darwin's proposed origin of species, over 30 species criteria have been brought forth and used to define species boundaries. In recent times, phylogenetic analyses based on multiple loci have been extensively used as a method to define species boundaries. However, only a few mycologists are aware that phylogenetic species criteria can mask discordances among fungal groups, leading to inaccurately defined species boundaries. In the current review, we discuss species recognition criteria, how and where these criteria can be applied along with their limitations and derived alternatives. In order to delimit fungal species, authors need to take into account not only the phylogenetic and phenotypic coherence, but also the timing of events that lead to fungal speciation and subsequent diversifications. Variations in the rate of phenotypic diversifications and convergent fungal evolution make it difficult to establish a universal species recognition criterion. The best practice can only be defined in the context of each fungal group. In this review, we provide a set of guidelines, encouraging an integrative taxonomic approach for species delimitation that can be used to define fungal species boundaries in the future. The other papers in this special issue deal with fungal speciation in Ascomycota, Dothideomycetes, Basidiomycota, basal fungi, lichen-forming fungi, plant pathogenic fungi, and yeasts.
44 citations
TL;DR: Overall, this paper considers that species delimitation in lichen-forming fungi has advanced dramatically over the past three decades, resulting in a solid framework, but that empirical evidence is still missing for many taxa.
Abstract: Lichens are symbiotic associations resulting from interactions among fungi (primary and secondary mycobionts), algae and/or cyanobacteria (primary and secondary photobionts), and specific elements of the bacterial microbiome associated with the lichen thallus. The question of what is a species, both concerning the lichen as a whole and its main fungal component, the primary mycobiont, has faced many challenges throughout history and has reached new dimensions with the advent of molecular phylogenetics and phylogenomics. In this paper, we briefly revise the definition of lichens and the scientific and vernacular naming conventions, concluding that the scientific, Latinized name usually associated with lichens invariably refers to the primary mycobiont, whereas the vernacular name encompasses the entire lichen. Although the same lichen mycobiont may produce different phenotypes when associating with different photobionts or growing in axenic culture, this discrete variation does not warrant the application of different scientific names, but must follow the principle "one fungus = one name". Instead, broadly agreed informal designations should be used for such discrete morphologies, such as chloromorph and cyanomorph for lichens formed by the same mycobiont but with either green algae or cyanobacteria. The taxonomic recognition of species in lichen-forming fungi is not different from other fungi and conceptual and nomenclatural approaches follow the same principles. We identify a number of current challenges and provide recommendations to address these. Species delimitation in lichen-forming fungi should not be tailored to particular species concepts but instead be derived from empirical evidence, applying one or several of the following principles in what we call the LPR approach: lineage (L) coherence vs. divergence (phylogenetic component), phenotype (P) coherence vs. divergence (morphological component), and/or reproductive (R) compatibility vs. isolation (biological component). Species hypotheses can be established based on either L or P, then using either P or L (plus R) to corroborate them. The reliability of species hypotheses depends not only on the nature and number of characters but also on the context: the closer the relationship and/or similarity between species, the higher the number of characters and/or specimens that should be analyzed to provide reliable delimitations. Alpha taxonomy should follow scientific evidence and an evolutionary framework but should also offer alternative practical solutions, as long as these are scientifically defendable. Taxa that are delimited phylogenetically but not readily identifiable in the field, or are genuinely cryptic, should not be rejected due to the inaccessibility of proper tools. Instead, they can be provisionally treated as undifferentiated complexes for purposes that do not require precise determinations. The application of infraspecific (gamma) taxonomy should be restricted to cases where there is a biological rationale, i.e., lineages of a species complex that show limited phylogenetic divergence but no evidence of reproductive isolation. Gamma taxonomy should not be used to denote discrete phenotypical variation or ecotypes not warranting the distinction at species level. We revise the species pair concept in lichen-forming fungi, which recognizes sexually and asexually reproducing morphs with the same underlying phenotype as different species. We conclude that in most cases this concept does not hold, but the actual situation is complex and not necessarily correlated with reproductive strategy. In cases where no molecular data are available or where single or multi-marker approaches do not provide resolution, we recommend maintaining species pairs until molecular or phylogenomic data are available. This recommendation is based on the example of the species pair Usnea aurantiacoatra vs. U. antarctica, which can only be resolved with phylogenomic approaches, such as microsatellites or RADseq. Overall, we consider that species delimitation in lichen-forming fungi has advanced dramatically over the past three decades, resulting in a solid framework, but that empirical evidence is still missing for many taxa. Therefore, while phylogenomic approaches focusing on particular examples will be increasingly employed to resolve difficult species complexes, broad screening using single barcoding markers will aid in placing as many taxa as possible into a molecular matrix. We provide a practical protocol how to assess and formally treat taxonomic novelties. While this paper focuses on lichen fungi, many of the aspects discussed herein apply generally to fungal taxonomy. The new combination Arthonia minor (Lucking) Lucking comb. et stat. nov. (Bas.: Arthonia cyanea f. minor Lucking) is proposed.
41 citations
TL;DR: This article provides descriptions and illustrations of microfungi associated with the leaf litter of Celtis formosana, Ficus ampelas, F. septica, Macaranga tanarius and Morus australis collected from Taiwan.
Abstract: This article provides descriptions and illustrations of microfungi associated with the leaf litter of Celtis formosana, Ficus ampelas, F. septica, Macaranga tanarius and Morus australis collected from Taiwan. These host species are native to the island and Celtis formosana is an endemic tree species. The study revealed 95 species, consisting of two new families (Cylindrohyalosporaceae and Oblongohyalosporaceae), three new genera (Cylindrohyalospora, Neodictyosporium and Oblongohyalospora), 41 new species and 54 new host records. The newly described species are Acrocalymma ampeli (Acrocalymmaceae), Arthrinium mori (Apiosporaceae), Arxiella celtidis (Muyocopronaceae), Bertiella fici (Melanommataceae), Cercophora fici (Lasiosphaeriaceae), Colletotrichum celtidis, C. fici, C. fici-septicae (Glomerellaceae), Conidiocarpus fici-septicae (Capnodiaceae), Coniella fici (Schizoparmaceae), Cylindrohyalospora fici (Cylindrohyalosporaceae), Diaporthe celtidis, D. fici-septicae (Diaporthaceae), Diaporthosporella macarangae (Diaporthosporellaceae), Diplodia fici-septicae (Botryosphaeriaceae), Discosia celtidis, D. fici (Sporocadaceae), Leptodiscella sexualis (Muyocopronaceae), Leptospora macarangae (Phaeosphaeriaceae), Memnoniella alishanensis, M. celtidis, M. mori (Stachybotryaceae), Micropeltis fici, M. ficina (Micropeltidaceae), Microthyrium fici-septicae (Microthyriaceae), Muyocopron celtidis, M. ficinum, Mycoleptodiscus alishanensis (Muyocopronaceae), Neoanthostomella fici (Xylariales genera incertae sedis), Neodictyosporium macarangae (Sordariales genera incertae sedis), Neofusicoccum moracearum (Botryosphaeriaceae), Neophyllachora fici (Phyllachoraceae), Nigrospora macarangae (Apiosporaceae), Oblongohyalospora macarangae (Oblongohyalosporaceae), Ophioceras ficinum (Ophioceraceae), Parawiesneriomyces chiayiensis (Wiesneriomycetaceae), Periconia alishanica, P. celtidis (Periconiaceae), Pseudocercospora fici-septicae (Mycosphaerellaceae), Pseudoneottiospora cannabacearum (Chaetosphaeriaceae) and Pseudopithomyces mori (Didymosphaeriaceae). The new host records are Alternaria burnsii, A. pseudoeichhorniae (Pleosporaceae), Arthrinium hydei, A. malaysianum, A. paraphaeospermum, A. rasikravindrae, A. sacchari (Apiosporaceae), Bartalinia robillardoides (Sporocadaceae), Beltrania rhombica (Beltraniaceae), Cladosporium tenuissimum (Cladosporiaceae), Coniella quercicola (Schizoparmaceae), Dematiocladium celtidicola (Nectriaceae), Diaporthe limonicola, D. millettiae, D. pseudophoenicicola (Diaporthaceae), Dictyocheirospora garethjonesii (Dictyosporiaceae), Dimorphiseta acuta (Stachybotryaceae), Dinemasporium parastrigosum (Chaetosphaeriaceae), Discosia querci (Sporocadaceae), Fitzroyomyces cyperacearum (Stictidaceae), Gilmaniella bambusae (Ascomycota genera incertae sedis), Hermatomyces biconisporus (Hermatomycetaceae), Lasiodiplodia thailandica, L. theobromae (Botryosphaeriaceae), Memnoniella echinata (Stachybotryaceae), Muyocopron dipterocarpi, M. lithocarpi (Muyocopronaceae), Neopestalotiopsis asiatica, N. phangngaensis (Sporocadaceae), Ophioceras chiangdaoense (Ophioceraceae), Periconia byssoides (Periconiaceae), Pestalotiopsis dracaenea, P. formosana, P. neolitseae, P. papuana, P. parva, P. portugallica, P. trachycarpicola (Sporocadaceae), Phragmocapnias betle (Capnodiaceae), Phyllosticta capitalensis (Phyllostictaceae), Pseudopestalotiopsis camelliae-sinensis (Sporocadaceae), Pseudopithomyces chartarum, P. sacchari (Didymosphaeriaceae), Pseudorobillarda phragmitis (Pseudorobillardaceae), Robillarda roystoneae (Sporocadaceae), Sirastachys castanedae, S. pandanicola (Stachybotryaceae),
Spegazzinia musae (Didymosphaeriaceae), Stachybotrys aloeticola, S. microspora (Stachybotryaceae), Strigula multiformis (Strigulaceae), Torula fici (Torulaceae), Wiesneriomyces laurinus (Wiesneriomycetaceae) and Yunnanomyces pandanicola (Sympoventuriaceae). The taxonomic placement of most taxa discussed in this study is based on morphological observation of specimens, coupled with multi-locus phylogenetic analyses of sequence data. In addition, this study provides a host-fungus database for future studies and increases knowledge of fungal diversity, as well as new fungal discoveries from the island.
35 citations
TL;DR: It is argued that a single property to delineate species boundaries has various defects and each species concept comes with its own advantages and disadvantages and several examples for ideal and pragmatic approaches of species delimitation are provided.
Abstract: Biodiversity loss from disturbances caused by human activities means that species are disappearing at an ever increasing rate. The high number of species that have yet to be described have generated extreme crisis to the taxonomist. Therefore, more than in any other era, effective ways to discover and delimitate species are needed. This paper reviews the historically foremost approaches used to delimit species in Ascomycota, the most speciose phylum of Fungi. These include morphological, biological, and phylogenetic species concepts. We argue that a single property to delineate species boundaries has various defects and each species concept comes with its own advantages and disadvantages. Recently the rate of species discovery has increased because of the advancement of phylogenetic approaches. However, traditional phylogenetic methods with few gene regions lack species-level resolution, and do not allow unambiguous conclusions. We detail the processes that affect gene tree heterogeneity, which acts as barriers to delimiting species boundaries in classical low-rank phylogenies. So far, limited insights were given to the DNA-based methodologies to establish well-supported boundaries among fungal species. In addition to reviewing concepts and methodologies used to delimit species, we present a case study. We applied different species delimitation methods to understand species boundaries in the plant pathogenic and cryptic genus Phyllosticta (Dothideomycetes, Botryosphaeriales). Several DNA-based methods over-split the taxa while in some methods several taxa fall into a single species. These problems can be resolved by using multiple loci and coalescence-based methods. Further, we discuss integrative approaches that are crucial for understanding species boundaries within Ascomycota and provide several examples for ideal and pragmatic approaches of species delimitation.
31 citations
TL;DR: In this paper, the authors discuss what a fungal species is and how identification of species in plant pathology has changed over the past decades, and provide guidelines to be considered when introducing a new species in a plant pathogenic genus.
Abstract: Scientific names are crucial for communicating knowledge concerning fungi and fungus-like organisms. In plant pathology, they link information regarding biology, host range, distribution and potential risk to agriculture and food security. In the past, delimitation among pathogenic taxa was primarily based on morphological characteristics. Due to distinct species sharing overlapping characteristics, the morphological identification of species is often neither straightforward nor reliable. Hence, the phylogenetic species concept based on molecular phylogenetic reconstructions gained importance. The present opinion discusses what a fungal species is and how identification of species in plant pathology has changed over the past decades. In this context, host-specialization and species complexes are discussed. Furthermore, species concepts in plant pathology are examined using case studies from Bipolaris, Colletotrichum, Curvularia, Diaporthe, Diplodia, Meliola, Plasmopara, rust fungi and Trichoderma. Each entry contains a brief introduction to the genus, concepts used in species identification so far and the problems in describing a species followed by recommendations. The importance of correctly naming and identifying a species is addressed in the context of recent introductions, and we also discuss whether the introduction of new species in pathogenic genera has been overestimated. We also provide guidelines to be considered when introducing a new species in a plant pathogenic genus.
University of Tartu1, Swedish University of Agricultural Sciences2, University of the Punjab3, Del Rosario University4, University of Antioquia5, University of Palermo6, Royal Botanic Gardens7, University of Cagliari8, Ghent University9, International Institute of Minnesota10, University of Dschang11, Uppsala University12, University of Duisburg-Essen13, Botswana International University of Science and Technology14, American Museum of Natural History15, Academy of Sciences of the Czech Republic16, Pondicherry University17, British Antarctic Survey18, University of Copenhagen19, Saint Mary's University20, Altai State University21, Commonwealth Scientific and Industrial Research Organisation22, Manchester Metropolitan University23, Hobart Corporation24, Utah Valley University25, Michigan State University26, Agricultural University of Iceland27, Wageningen University and Research Centre28, Qatar University29, National Autonomous University of Mexico30, Mae Fah Luang University31, Estonian University of Life Sciences32, University of Ilorin33, Syracuse University34, State University of New York College of Environmental Science and Forestry35, Quaid-i-Azam University36, Universidade Federal de Sergipe37, University of the Free State38, Chinese Academy of Sciences39, University of Gothenburg40, Autonomous University of Coahuila41, Austral University of Chile42, King Saud University43, Moscow State University44, United Arab Emirates University45, Humboldt State University46, Seoul National University47, Goethe University Frankfurt48, Forest Research Institute49
TL;DR: The Global Soil Mycobiome Consortium (GSMc) dataset as mentioned in this paper contains 722,682 fungal operational taxonomic units (OTUs) derived from PacBio sequencing of full-length ITS and 18S-V9 variable regions from 3200 plots in 108 countries on all continents.
Abstract: Fungi are highly important biotic components of terrestrial ecosystems, but we still have a very limited understanding about their diversity and distribution. This data article releases a global soil fungal dataset of the Global Soil Mycobiome consortium (GSMc) to boost further research in fungal diversity, biogeography and macroecology. The dataset comprises 722,682 fungal operational taxonomic units (OTUs) derived from PacBio sequencing of full-length ITS and 18S-V9 variable regions from 3200 plots in 108 countries on all continents. The plots are supplied with geographical and edaphic metadata. The OTUs are taxonomically and functionally assigned to guilds and other functional groups. The entire dataset has been corrected by excluding chimeras, index-switch artefacts and potential contamination. The dataset is more inclusive in terms of geographical breadth and phylogenetic diversity of fungi than previously published data. The GSMc dataset is available over the PlutoF repository.
TL;DR: P phylogenetic species concepts that employ sequence data of rDNA and other genes are universally applied in fungal taxonomy, including yeasts, because various studies revealed a relatively good correlation between the biological species concept and sequence divergence.
Abstract: Here we review how evolving species concepts have been applied to understand yeast diversity. Initially, a phenotypic species concept was utilized taking into consideration morphological aspects of colonies and cells, and growth profiles. Later the biological species concept was added, which applied data from mating experiments. Biophysical measurements of DNA similarity between isolates were an early measure that became more broadly applied with the advent of sequencing technology, leading to a sequence-based species concept using comparisons of parts of the ribosomal DNA. At present phylogenetic species concepts that employ sequence data of rDNA and other genes are universally applied in fungal taxonomy, including yeasts, because various studies revealed a relatively good correlation between the biological species concept and sequence divergence. The application of genome information is becoming increasingly common, and we strongly recommend the use of complete, rather than draft genomes to improve our understanding of species and their genome and genetic dynamics. Complete genomes allow in-depth comparisons on the evolvability of genomes and, consequently, of the species to which they belong. Hybridization seems a relatively common phenomenon and has been observed in all major fungal lineages that contain yeasts. Note that hybrids may greatly differ in their post-hybridization development. Future in-depth studies, initially using some model species or complexes may shift the traditional species concept as isolated clusters of genetically compatible isolates to a cohesive speciation network in which such clusters are interconnected by genetic processes, such as hybridization.
TL;DR: This is a multidimensional review of mangrove fungi occurring as saprobes, pathogens and endophytes of a wide range of host substrates and those isolated from the water columns and sediments in mangroves.
Abstract: This is a multidimensional review of mangrove fungi occurring as saprobes, pathogens and endophytes of a wide range of host substrates and those isolated from the water columns and sediments in mangroves. Eight-hundred and fifty taxa including 658 that are supported by both morphology and molecular data and 192 with only morphological data are listed. These constitute Ascomycota, the dominant group with 773 species, and 58 Basidiomycota, one Blastocladiomycota, five Chytridiomycota, and 13 Mucoromycota. This study also includes data on mangrove yeasts 103 Ascomycota, 39 Basidiomycota and 193 taxa isolated from sediments. Endophytes isolated from submerged parts of mangrove plants total 38. The most specious orders of mangrove fungi are Pleosporales 133, Saccharomycetales 102, Microascales 101, Eurotiales 87, Hypocreales 60 and Xylariales 54. Speciose genera include Candida 39, Aspergillus 53, Penicillium 17 and Corollospora 16. The highest number of mangrove fungi have been recorded from the Pacific Ocean 553, which is the largest ocean, followed by Indian 408 and Atlantic Oceans 259. Geographical distribution of mangrove fungi varied from ocean to ocean with only 109 taxa common to the Atlantic, Indian and Pacific Oceans. Of the various countries reported for mangrove fungi, India accommodates the highest number (339) followed by Thailand 303, Malaysia 171, Florida Everglades, USA 134 and Brunei 134. A total of 60 different mangrove plants and their associates have been surveyed for mangrove fungi. These results are discussed and compared with previous studies.
TL;DR: Cancellidium is a remarkable fungal genus which has been collected from wood submerged in freshwater and has unique conidia that are important in dispersal in running streams as mentioned in this paper.
Abstract: Cancellidium is a remarkable fungal genus which has been collected from wood submerged in freshwater and has unique conidia that are important in dispersal in running streams. With such a remarkable morphology, one would have expected it to be a distinct family or order. However, due to the dearth of molecular evidence in related taxa, this genus has previously been placed in the order Hypocreales, subclass Hypocreomycetidae of Sordariomycetes. In this study, we made three new collections of this remarkable aquatic genus from streams in China and Thailand, isolated them into culture, extracted DNA and carried out multigene phylogenetic analysis and divergence time estimation which placed the genus in Diaporthomycetidae. This is one of the seven subclasses of Sordariomycetes and contains 30 lineages that are only known from freshwater. The subclass is therefore of interest when considering the evolution of freshwater fungi. Several lineages of Diaporthomycetidae are morphologically unique and taxa cluster with strong support, but have weak support at the base of the trees. The phylogenetic and MCC trees generated in this study indicate that Aquapteridospora, Barbatosphaeriaceae, Bullimyces, Cancellidium, Ceratolenta, Conlarium, Phialemoniopsis, Pseudostanjehughesia and Rhamphoriaceae are distinct genera/families that evolved in the family/order time frame. The new orders Barbatosphaeriales (177 MYA), Cancellidiales (137 MYA), Ceratolentales (147 MYA), Conlariales (138 MYA) and Rhamphoriales (133 MYA) and six new families, Aquapteridosporaceae (110 MYA), Cancellidiaceae (137 MYA), Ceratolentaceae (81 MYA), Bullimycetaceae (81 MYA), Phialemoniopsaceae (59 MYA), and Pseudostanjehughesiaceae (111 MYA) are introduced with evidence from phylogenies, divergence estimates and distinct morphologies. Of these families, Aquapteridosporaceae, Cancellidiaceae, Bullimycetaceae, and Pseudostanjehughesiaceae are only known from freshwater.
TL;DR: Four commonly used species concepts, focusing on morphological, ecological, biological and phylogenetic criteria and their applicability in the taxonomy of Dothideomycetes are reviewed.
Abstract: The species is one of the basic units of biological classification. Both species concepts and recognition are essential topics in taxonomic studies and other biological research. In the first part of this review, we briefly discuss the taxonomic history of the class Dothideomycetes. In the second part of the paper, we review four commonly used species concepts, focusing on morphological, ecological, biological and phylogenetic criteria and their applicability in the taxonomy of Dothideomycetes. The application and utility of the four criteria is discussed with examples in the genera Ascochyta, Cercospora and Neofusicoccum. Some problems and challenges of studying Dothideomycetes are analyzed and basic guidelines for classifying species under the above criteria are provided.
University of Jena1, Leibniz Association2, University of Michigan3, Royal Botanic Gardens4, Federal University of Pernambuco5, Oklahoma State University–Stillwater6, Seoul National University7, Aberystwyth University8, Free University of Berlin9, Technische Universität München10, Mae Fah Luang University11, Chonnam National University12
TL;DR: In this article, the taxonomy of the basal fungi is reviewed and the relationships among early-diverging lineages of fungal phyla are discussed. And a new type species, Nephridiophaga blattellae, is proposed.
Abstract: The increasing number of new fungal species described from all over the world along with the use of genetics to define taxa, has dramatically changed the classification system of early-diverging fungi over the past several decades. The number of phyla established for non-Dikarya fungi has increased from 2 to 17. However, to date, both the classification and phylogeny of the basal fungi are still unresolved. In this article, we review the recent taxonomy of the basal fungi and re-evaluate the relationships among early-diverging lineages of fungal phyla. We also provide information on the ecology and distribution in Mucoromycota and highlight the impact of chytrids on amphibian populations. Species concepts in Chytridiomycota, Aphelidiomycota, Rozellomycota, Neocallimastigomycota are discussed in this paper. To preserve the current application of the genus Nephridiophaga (Chytridiomycota: Nephridiophagales), a new type species, Nephridiophaga blattellae, is proposed.
Chinese Academy of Sciences1, Sewanee: The University of the South2, Ghent University3, Purdue University4, Ruhr University Bochum5, University of Amsterdam6, Utrecht University7, Universidade Federal de Santa Catarina8, University of Salamanca9, University of Ljubljana10, Mae Fah Luang University11, Zhongkai University of Agriculture and Engineering12, Kunming Institute of Botany13, Agricultural University of Hebei14, Naturalis15, University of Agriculture, Faisalabad16, University of Tartu17, Butler University18, Goethe University Frankfurt19, Mendel University20, Ministry for Primary Industries21, University of Turin22, Leibniz Association23, Uppsala University24
TL;DR: The second largest phylum of Fungi, Basidiomycota, contains some of the best known species of mushrooms, rusts, smuts, and jelly fungi as discussed by the authors.
Abstract: Species delimitation is one of the most fundamental processes in biology. Biodiversity undertakings, for instance, require explicit species concepts and criteria for species delimitation in order to be relevant and translatable. However, a perfect species concept does not exist for Fungi. Here, we review the species concepts commonly used in Basidiomycota, the second largest phylum of Fungi that contains some of the best known species of mushrooms, rusts, smuts, and jelly fungi. In general, best practice is to delimitate species, publish new taxa, and conduct taxonomic revisions based on as many independent lines of evidence as possible, that is, by applying a so-called unifying (or integrative) conceptual framework. However, the types of data used vary considerably from group to group. For this reason we discuss the different classes of Basidiomycota, and for each provide: (i) a general introduction with difficulties faced in species recognition, (ii) species concepts and methods for species delimitation, and (iii) community recommendations and conclusions.
TL;DR: It is necessary to identify phytopathogens to species level based on data from multiple approaches and this identification must go beyond species level to clearly classify hitherto known subspecies, forms and races.
Abstract: In plant pathology, the correct naming of a species is essential for determining the causal agents of disease. Species names not only serve the general purpose of concise communication, but also are critical for effective plant quarantine, preventing the introduction of new pathogens into a territory. Many phytopathogenic genera have multiple species and, in several genera, disagreements between the multiple prevailing species concept definitions result in numerous cryptic species. Some of these species were previously called by various names; forma speciales (specialised forms), subspecies, or pathotypes. However, based on new molecular evidence they are being assigned into new species. The frequent name changes and lack of consistent criteria to delineate cryptic species, species, subspecies, forms, and races create increasing confusion, often making communication among biologists arduous. Furthermore, such ambiguous information can convey misleading evolutionary concepts and species boundaries. The aim of this paper is to review these concepts, clarify their use, and evaluate them by referring to existing examples. We specifically address the question, “Do plant pathogens require a different ranking system?” We conclude that it is necessary to identify phytopathogens to species level based on data from multiple approaches. Furthermore, this identification must go beyond species level to clearly classify hitherto known subspecies, forms and races. In addition, when naming phytopathogenic genera, plant pathologists should provide more information about geographic locations and host ranges as well as host specificities for individual species, cryptic species, forms or races. When describing a new phytopathogen, we suggest that authors provide at least three representative strains together with pathogenicity test results. If Koch’s postulates cannot be fulfilled, it is necessary to provide complementary data such as associated disease severity on the host plant. Moreover, more sequenced collections of species causing diseases should be published in order to stabilise the boundaries of cryptic species, species, subspecies, forms, and races.
TL;DR: 34 new species are formally described and three new families Endoraeciaceae, Neophysopellaceae and Uromycladiaceae are proposed based on their morphological distinctions, phylogenetic independences and divergent times in Pucciniales.
Abstract: Rust fungi taxonomically belonging to Pucciniales (Basidiomycota) are important phytopathogens that cause many significant diseases to agricultural crops and forest trees. Hitherto, ca. 8000 and 1200 species have been reported from worldwide and China, respectively. To investigate and document the diversity of rust fungi in China, we have sampled from 86 natural reserves and national parks in the past several years, and 6627 specimens have been collected. Our identification using both morphological and molecular data assigned 1654 collections to 337 species in 43 genera of 15 families, as cataloged in this paper. Among them, 34 new species are formally described based on their morphological distinctions and phylogenetic relationships. In addition, three new families Endoraeciaceae, Neophysopellaceae and Uromycladiaceae are proposed based on their morphological distinctions, phylogenetic independences and divergent times. Considering the traditionally morphologically defined families in Pucciniales have been increasing revealed to be discordant with phylogenetic groupings, taxonomic revisions are needed in future study to establish a natural classification system in Pucciniales. We also discussed the importance of morphologies in spermogonia and aecia for the delimitation of Puccinia and related genera. This study presents a significant contribution to the knowledge of rust flora in China. Taxonomic novelties: new families: Endoraeciaceae P. Zhao & L. Cai; Neophysopellaceae P. Zhao & L. Cai; Uromycladiaceae P. Zhao & L. Cai; new species: Chrysomyxa jinghongensis P. Zhao & L. Cai; Coleosporium sichuanense P. Zhao & L. Cai; Coleosporium smilacis P. Zhao & L. Cai; Cystopsora yunnanense P. Zhao & L. Cai; Gerwasia guanganensis P. Zhao & L. Cai; Gerwasia rubus-playfairianus P. Zhao & L. Cai; Hamaspora rubus-pirifolius P. Zhao & L. Cai; Macruropyxis guizhouensis P. Zhao & L. Cai; Macruropyxis paederiae P. Zhao & L. Cai; Melampsora hyperici-sampsonii P. Zhao & L. Cai; Melampsora linearis P. Zhao & L. Cai; Melampsora salicis-delavayanae P. Zhao & L. Cai; Neophysopella vitis-davidii P. Zhao & L. Cai; Phakopsora sophorae P. Zhao & L. Cai; Phragmidium nonapiculatum P. Zhao & L. Cai; Phragmidium kanas P. Zhao & L. Cai; Phragmidium duchesneae-indicae P. Zhao & L. Cai; Pileolaria medogensis P. Zhao & L. Cai; Puccinia amygdalus-iridis P. Zhao & L. Cai; Puccinia aphananthe-aspera P. Zhao & L. Cai; Puccinia microsorus P. Zhao & L. Cai; Puccinia nandina-domestica P. Zhao & L. Cai; Puccinia persicaria-odorata P. Zhao & L. Cai; Puccinia polygonum-aviculare P. Zhao & L. Cai; Puccinia pulverulentus P. Zhao & L. Cai; Puccinia saposhnikoviae P. Zhao & L. Cai; Puccinia sonchus-oleraceus P. Zhao & L. Cai; Puccinia thalictrum-finetii P. Zhao & L. Cai; Puccinia thalictrum-minus P. Zhao & L. Cai; Puccinia xingwenensis P. Zhao & L. Cai; Puccinia xinjiangensis P. Zhao & L. Cai; Puccinia zanthoxyli-chinensis P. Zhao & L. Cai; Uromyces aconiticola P. Zhao & L. Cai; Uromycladium yunnanense P. Zhao & L. Cai; new combinations: Chrysomyxa purpurea (C.J. You & J. Cao) P. Zhao & L. Cai; Neophysopella verannonae (Beenken) P. Zhao & L. Cai.
TL;DR: The analysis estimated proto-appressoria diversification during the Mesozoic period (92–239 million years ago), however, its origin remains inconclusive, and data suggest that these hyaline appressia diversified into melanized or compound appressoria, with evidence of adaptive radiation.
Abstract: Fungi have evolved diverse strategies to acquire nutrients as endophytes, saprobes, symbionts, or pathogens. Appressoria have been intensively studied due to their importance in attaching and breaching the host surface. These specialized infection structures have evolved into various morpho-types: proto-appressoria, hyaline appressoria, melanized (dark) appressoria, and compound appressoria. In this review, we discuss the differences in the formation, differentiation, and function of appressoria among fungi with diverse life strategies. Using DNA sequence information, LSU, 5.8S, SSU and rpb2 gene fragments, we reconstructed the ancestral states for appressorial types in the main phyla of fungi and fungus-like organisms and found that the hyaline appressoria was the most ancestral form. Our analysis estimated proto-appressoria diversification during the Mesozoic period (92–239 million years ago), however, its origin remains inconclusive. Our data suggest that these hyaline appressoria diversified into melanized or compound appressoria, with evidence of adaptive radiation.
TL;DR: In this article, the taxonomy of several unusual fungal genera collected in a range of aquatic and terrestrial environments in Oman were identified based on phylogenetic analyses of nuclear ribosomal DNA (rDNA) (LSU, SSU and ITS) and protein-coding genes (TEF, RPB2 and TUB).
Abstract: Hot desert regions are undoubtedly challenging to fungal survival on the Arabian Peninsula. Fungi are, however, recognized as the most stress-resistant organisms among all eukaryotes, which could be a result of the rapid evolution of distinct species. Our current understanding of these microorganisms is derived from studies examining only a fraction of the overall fungal diversity. Therefore, further studies are needed to understand the diversity of fungi in desert regions. This paper highlights the taxonomy of several unusual fungal genera collected in a range of aquatic and terrestrial environments in Oman. These taxa were identified based on phylogenetic analyses of nuclear ribosomal DNA (rDNA) (LSU, SSU and ITS) and protein-coding genes (TEF, RPB2 and TUB), plus morphological comparisons. Phylogenetic analyses, including the presently recognized genera in Patellariales resulted in splitting the order into four clades in Dothideomycetes. The new family Holmiellaceae and new order Holmiellales are introduced to include Holmiella. Species of Homortomycetaceae form a well-supported and distinct clade and raise it to Homortomycetales ordo novus. Omania (Halojulellaceae), Desertiserpentica (Lophiostomataceae) and Montanitestudina (Testudinaceae) are described as novel genera in Dothideomycetes. A synnematous hyphomycete with basidiomycetous affinity (Corticiales) was also identified and described as Basidiodesertica. Additionally, an asexual morph was observed for Holmiella junipericola; Patellaria quercus is synonymized under P. atrata, and seven new species are described.
TL;DR: The main objective in this study is to revise and update the taxonomy of several well-known old and poorly studied species whose classification are still obscure and establish a new genus Neoschizothecium based on phylogenetic analysis.
Abstract: Sordariomycetes is an earlier-introduced and one of the widely distributed class of Ascomycota. The class was initially classified based on morphology in having inoperculate and unitunicate asci. With the development of DNA based phylogenetic analysis, several undetermined or polyphyletic members of Sordariomycetes were reclassified. However, not all species belonging to this class have been sequenced and analyzed. There are a number of species, especially those old and poorly studied ones which have never been sequenced before and not even recollected again for further taxonomic verification. One of the main objective in this study is to revise and update the taxonomy of several well-known early and poorly studied species whose classification are still obscure. Herein, we re-examined the type materials and/or authentic specimens together to explore 74 relatively poorly-studied genera, which mainly belong to Boliniales, Calosphaeriales, Chaetosphaeriales, Jobellisiales, and Sordariales classified under Diaporthomycetidae and Sordariomycetidae. We provide descriptions, notes, figures and/or drawings and discussed their phylogenetic relationships. As a result, the monotypic Jobellisiales is transferred from Hypocreomycetidae to Diaporthomycetidae. Based on phylogenetic analysis, the polyphyletic Lasiosphaeriaceae is divided into five families, Bombardiaceae (Apodospora, Bombardia, Bombardioidea, Fimetariella and Ramophialophora), Lasiosphaeriaceae (Anopodium, Bellojisia, Corylomyces, Lasiosphaeria, Mammaria and Zopfiella), Lasiosphaeridaceae (Lasiosphaeris), Strattoniaceae (Strattonia) and Zygospermellaceae (Episternus and Zygospermella). In addition, a new family Neoschizotheciaceae is established based on Neoschizothecium. Analysis of the type species of Boothiella, Stellatospora, Sulcatistroma and Tengiomyces placed them in Sordariaceae, Chaetomiaceae, Hypocreales and Coronophorales, respectively. We classify the genera lacking molecular data based on their morphology and expect them to be recollected; that is, Kacosphaeria in Calosphaeriales; Arnium, Biconiosporella, Camptosphaeria, Diffractella, Emblemospora, Eosphaeria, Periamphispora, Synaptospora and Tripterosporella in Sordariales; Conidiotheca in Sordariomycetes; Copromyces, Effetia, Endophragmiella and Tulipispora are accommodated in Ascomycota. Besides, we establish a new genus Neoschizothecium based on phylogenetic analysis. New combinations proposed: Camaropella amorpha, Cam. microspora, Cam. plana, Cladorrhinum grandiusculum, Cla. leucotrichum, Cla. terricola, Cla. olerum, Helminthosphaeria plumbea, Immersiella hirta, Jugulospora minor, Lasiosphaeris arenicola, Neoschizothecium aloides, Neo. carpinicola, Neo. conicum, Neo. curvisporum, Neo. fimbriatum, Neo. glutinans, Neo. inaequale, Neo. minicaudum, Neo. selenosporum, Neo. tetrasporum, Neurospora autosteira, Podospora brunnescens, P. flexuosa, P. jamaicensis, P. hamata, P. macrospora, P. spinosa, Strattonia petrogale and Triangularia microsclerotigena, T. nannopodalis, T. praecox, T. samala, T. tarvisina, T. unicaudata, T. yaeyamensis. New epithets are proposed for Apiorhynchostoma apiosporum and Podospora dacryoidea.
TL;DR: It is demonstrated how target capture approaches can effectively decipher ancient rapid radiations in cases where well resolved individual exon trees are sufficiently sampled and how to identify subsets of loci that are appropriate for fungal order-level phylogenetics.
Abstract: Rapid radiations in Fungi are only beginning to be studied with phylogenomic data. The evolutionary history of the lichenized fungal order Peltigerales has not been well resolved, particularly for the Collematineae. Here, we used concatenation and coalescent-based species tree methods to reconstruct the phylogeny of the Peltigerales based on sequences of 125 nuclear single-copy exon sequences among 60 samples, representing 58 species. Despite uneven, lineage-specific missing data and significant topological incongruence of individual exon trees, the resulting phylogenies were concordant and successfully resolved the phylogenetic relationships of the Peltigerales. Relationships in the Collematineae were defined by short branches and lower nodal support than in other parts of the tree, due in part to conflicting signal in exon trees, suggesting rapid diversification events in the early evolution of the suborder. Using tree distance measures, we were able to identify a minimum subset of exons that could reconstruct phylogenetic relationships in Peltigerales with higher support than the 125-exon dataset. Comparisons between the minimum and complete datasets in species tree inferences, bipartition analyses, and divergence time estimations displayed similar results, although the minimum dataset was characterized by higher levels of error in estimations of divergence times. Contrasting our inferences from the complete and minimum datasets to those derived from few nuclear and mitochondrial loci reveal that our topology is concordant with topologies reconstructed using the nuclear large subunit and mitochondrial small subunit ribosomal DNA markers, but the target capture datasets had much higher support values. We demonstrated how target capture approaches can effectively decipher ancient rapid radiations in cases where well resolved individual exon trees are sufficiently sampled and how to identify subsets of loci that are appropriate for fungal order-level phylogenetics.
TL;DR: A taxonomic revision of the Teichosporaceae based on morphological and phylogenetic evidence is presented in this paper. But the taxonomy of the family is not discussed in this paper.
Abstract: The placement of the dothideomycetous family Teichosporaceae has been controversial. Recent phylogenetic investigations have used a taxonomic lumping approach with the Floricolaceae and its genera have been synonymized under the earlier family name, Teichosporaceae. Intergeneric relationships were therefore obscure and proper generic delimitation was needed in upcoming studies. We here taxonomically revised the family Teichosporaceae based on both morphological and phylogenetic evidence. Teichosporaceae species have immersed or semi-immersed, erumpent to superficial, ostiolate ascomata, cellular or trabeculate pseudoparaphyses, cylindrical to oblong or sub-clavate asci and ellipsoid to oblong or fusiform, cylindric-fusiform or oblong to elliptical, ovoid to clavate, symmetric or asymmetric, initially hyaline or pale brown to dark brown or yellowish brown, 1–3-septate or muriform ascospores. Asexual morphs are coelomycetous. Type or representative specimens of Teichosporaceae were loaned and fresh specimens were collected from China and Thailand. Maximum likelihood and Bayesian analyses of a combined ITS, LSU, SSU, tef1-α and rpb2 dataset were performed to clarify the phylogenetic affinities of taxa and examine monophyly of newly proposed genera. One new species (Floricola festucae), one new host record (Ramusculicola thailandica) and four new combinations (Aurantiascoma nephelii, A. quercus, Magnibotryascoma acaciae, M. melanommoides) are introduced. The broad genus concept of Teichospora is dismissed based on morphological dissimilarities and the monophyletic status of the proposed genera. We accept Asymmetrispora, Aurantiascoma, Floricola, Magnibotryascoma, Misturatosphaeria, Pseudoaurantiascoma, Pseudomisturatosphaeria, Ramusculicola and Teichospora as distinct genera in the Teichosporaceae. All recognized genera are phenotypically characterized and phylogenetically well-supported. The phylogenetic placements of three genera (Chaetomastia, Loculohypoxylon and Sinodidymella), which do not have molecular data cannot be conclusively clarified at present, but are still placed in Teichosporaceae for future studies.