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 s...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.展开更多
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 si...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,Neocal-limastigomycota,Olpidiomycota,Rozellomycota,Sanchytriomycota,and Zoopagomycota.In the phylogenies,Caulochy-triomycota 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.展开更多
The previous phylogenies of Sordariomycetes by M.E.Barr,O.E.Eriksson and D.L.Hawksworth,and T.Lumbsch and S.Huhndorf,were mainly based on morphology and thus were somewhat subjective.Later outlines by T.Lumbsch and S....The previous phylogenies of Sordariomycetes by M.E.Barr,O.E.Eriksson and D.L.Hawksworth,and T.Lumbsch and S.Huhndorf,were mainly based on morphology and thus were somewhat subjective.Later outlines by T.Lumbsch and S.Huhndorf,and Maharachchikumbura and co-authors,took into account phylogenetic evidence.However,even these phylogenetic driven arrangements for Sordariomycetes,were somewhat subjective,as the arrangements in trees depended on many variables,such as number of taxa,different gene regions and methods used in the analyses.What is needed is extra evidence to help standardize ranking in the fungi.Estimation of divergence times using molecular clock methods has been proposed for providing additional rational for higher ranking of taxa.Thus,in Sordariomycetes,a divergence period(i.e.200–300 MYA)can be used as criteria to judge when a group of related taxa evolved and what rank they should be given.In this paper,we provide an updated classification of accepted subclasses,orders of Sordariomycetes and use divergence times to provide additional evidence to stabilize ranking of taxa in the class.We point out and discuss discrepancies where the phylogenetic tree conflicts with the molecular clock.展开更多
This article is the ninth in the series of Fungal Diversity Notes,where 107 taxa distributed in three phyla,nine classes,31 orders and 57 families are described and illustrated.Taxa described in the present study incl...This article is the ninth in the series of Fungal Diversity Notes,where 107 taxa distributed in three phyla,nine classes,31 orders and 57 families are described and illustrated.Taxa described in the present study include 12 new genera,74 new species,three new combinations,two reference specimens,a re-circumscription of the epitype,and 15 records of sexualasexual morph connections,new hosts and new geographical distributions.Twelve new genera comprise Brunneofusispora,Brunneomurispora,Liua,Lonicericola,Neoeutypella,Paratrimmatostroma,Parazalerion,Proliferophorum,Pseudoastrosphaeriellopsis,Septomelanconiella,Velebitea and Vicosamyces.Seventy-four new species are Agaricus memnonius,A.langensis,Aleurodiscus patagonicus,Amanita flavoalba,A.subtropicana,Amphisphaeria mangrovei,Baorangia major,Bartalinia kunmingensis,Brunneofusispora sinensis,Brunneomurispora lonicerae,Capronia camelliaeyunnanensis,Clavulina thindii,Coniochaeta simbalensis,Conlarium thailandense,Coprinus trigonosporus,Liua muriformis,Cyphellophora filicis,Cytospora ulmicola,Dacrymyces invisibilis,Dictyocheirospora metroxylonis,Distoseptispora thysanolaenae,Emericellopsis koreana,Galiicola baoshanensis,Hygrocybe lucida,Hypoxylon teeravasati,Hyweljonesia indica,Keissleriella caraganae,Lactarius olivaceopallidus,Lactifluus midnapurensis,Lembosia brigadeirensis,Leptosphaeria urticae,Lonicericola hyaloseptispora,Lophiotrema mucilaginosis,Marasmiellus bicoloripes,Marasmius indojasminodorus,Micropeltis phetchaburiensis,Mucor orantomantidis,Murilentithecium lonicerae,Neobambusicola brunnea,Neoeutypella baoshanensis,Neoroussoella heveae,Neosetophoma lonicerae,Ophiobolus malleolus,Parabambusicola thysanolaenae,Paratrimmatostroma kunmingensis,Parazalerion indica,Penicillium dokdoense,Peroneutypa mangrovei,Phaeosphaeria cycadis,Phanerochaete australosanguinea,Plectosphaerella kunmingensis,Plenodomus artemisiae,P.lijiangensis,Proliferophorum thailandicum,Pseudoastrosphaeriellopsis kaveriana,Pseudohelicomyces menglunicus,Pseudoplagiostoma mangiferae,Robillarda mangiferae,Roussoella elaeicola,Russula choptae,R.uttarakhandia,Septomelanconiella thailandica,Spencermartinsia acericola,Sphaerellopsis isthmospora,Thozetella lithocarpi,Trechispora echinospora,Tremellochaete atlantica,Trichoderma koreanum,T.pinicola,T.rugulosum,Velebitea chrysotexta,Vicosamyces venturisporus,Wojnowiciella kunmingensis and Zopfiella indica.Three new combinations are Baorangia rufomaculata,Lanmaoa pallidorosea and Wojnowiciella rosicola.The reference specimens of Canalisporium kenyense and Tamsiniella labiosa are designated.The epitype of Sarcopeziza sicula is re-circumscribed based on cyto-and histochemical analyses.The sexual-asexual morph connection of Plenodomus sinensis is reported from ferns and Cirsium for the first time.In addition,the new host records and country records are Amanita altipes,A.melleialba,Amarenomyces dactylidis,Chaetosphaeria panamensis,Coniella vitis,Coprinopsis kubickae,Dothiorella sarmentorum,Leptobacillium leptobactrum var.calidus,Muyocopron lithocarpi,Neoroussoella solani,Periconia cortaderiae,Phragmocamarosporium hederae,Sphaerellopsis paraphysata and Sphaeropsis eucalypticola.展开更多
This article is the tenth series of the Fungal Diversity Notes,where 114 taxa distributed in three phyla,ten classes,30 orders and 53 families are described and illustrated.Taxa described in the present study include ...This article is the tenth series of the Fungal Diversity Notes,where 114 taxa distributed in three phyla,ten classes,30 orders and 53 families are described and illustrated.Taxa described in the present study include one new family(viz.Pseudoberkleasmiaceae in Dothideomycetes),five new genera(Caatingomyces,Cryptoschizotrema,Neoacladium,Paramassaria and Trochilispora)and 71 new species,(viz.Acrogenospora thailandica,Amniculicola aquatica,A.guttulata,Angustimassarina sylvatica,Blackwellomyces lateris,Boubovia gelatinosa,Buellia viridula,Caatingomyces brasiliensis,Calophoma humuli,Camarosporidiella mori,Canalisporium dehongense,Cantharellus brunneopallidus,C.griseotinctus,Castanediella meliponae,Coprinopsis psammophila,Cordyceps succavus,Cortinarius minusculus,C.subscotoides,Diaporthe italiana,D.rumicicola,Diatrypella delonicis,Dictyocheirospora aquadulcis,D.taiwanense,Digitodesmium chiangmaiense,Distoseptispora dehongensis,D.palmarum,Dothiorella styphnolobii,Ellisembia aurea,Falciformispora aquatic,Fomitiporia carpinea,F.lagerstroemiae,Grammothele aurantiaca,G.micropora,Hermatomyces bauhiniae,Jahnula queenslandica,Kamalomyces mangrovei,Lecidella yunnanensis,Micarea squamulosa,Muriphaeosphaeria angustifoliae,Neoacladium indicum,Neodidymelliopsis sambuci,Neosetophoma miscanthi,N.salicis,Nodulosphaeria aquilegiae,N.thalictri,Paramassaria samaneae,Penicillium circulare,P.geumsanense,P.mali-pumilae,P.psychrotrophicum,P.wandoense,Phaeoisaria siamensis,Phaeopoacea asparagicola,Phaeosphaeria penniseti,Plectocarpon galapagoense,Porina sorediata,Pseudoberkleasmium chiangmaiense,Pyrenochaetopsis sinensis,Rhizophydium koreanum,Russula prasina,Sporoschisma chiangraiense,Stigmatomyces chamaemyiae,S.cocksii,S.papei,S.tschirnhausii,S.vikhrevii,Thysanorea uniseptata,Torula breviconidiophora,T.polyseptata,Trochilispora schefflerae and Vaginatispora palmae).Further,twelve new combinations(viz.Cryptoschizotrema cryptotrema,Prolixandromyces australi,P.elongatus,P.falcatus,P.longispinae,P.microveliae,P.neoalardi,P.polhemorum,P.protuberans,P.pseudoveliae,P.tenuistipitis and P.umbonatus),an epitype is chosen for Cantharellus goossensiae,a reference specimen for Acrogenospora sphaerocephala and new synonym Prolixandromyces are designated.Twenty-four new records on new hosts and new geographical distributions are also reported(i.e.Acrostalagmus annulatus,Cantharellus goossensiae,Coprinopsis villosa,Dothiorella plurivora,Dothiorella rhamni,Dothiorella symphoricarposicola,Dictyocheirospora rotunda,Fasciatispora arengae,Grammothele brasiliensis,Lasiodiplodia iraniensis,Lembosia xyliae,Morenoina palmicola,Murispora cicognanii,Neodidymelliopsis farokhinejadii,Neolinocarpon rachidis,Nothophoma quercina,Peroneutypa scoparia,Pestalotiopsis aggestorum,Pilidium concavum,Plagiostoma salicellum,Protofenestella ulmi,Sarocladium kiliense,Tetraploa nagasakiensis and Vaginatispora armatispora).展开更多
The history of assigning ranks to fungi,as well as the relative importance of using divergence time estimates is reviewed.The paper pays tribute to the major mycological players,and especially to David Hawksworth on h...The history of assigning ranks to fungi,as well as the relative importance of using divergence time estimates is reviewed.The paper pays tribute to the major mycological players,and especially to David Hawksworth on his 70th birthday and his contribution to fungal ranking in Systema Ascomycetum from 1982 to 1998.Following the conclusion of the latter series,the ranking continued with the Outlines of Ascomycota in 2007 and 2010 and more recently with specific classes in‘Towards an outline of Sordariomycetes’and‘Families of Dothideomycetes’.Earlier classifications based on phenotype were certainly more subjective;however,remarkably many of these old arrangements have stood the test of time.More recently,phylogenetic analyses have provided evidence towards a natural classification,resulting in significant changes in many lineages.The classification arrangements however,are still subjective and dependent on the taxa analysed,resulting in different taxonomic interpretations and schemes,particularly when it comes to ranking.Thus,what have been considered as genera by some,have been introduced as families by others.More recently,estimation of divergence times using molecular clock methods have been used as objective evidence for higher ranking of taxa.A divergence period(i.e.200–300 MYA)can be used as a criterion to infer when a group of related taxa evolved and what rank they should be given.We compiled data on divergence times for various higher ranking taxa in the Kingdom Fungi.The kingdom evolved 1000–1600 MYA(Stenian–Calymmian),while the presently accepted phyla evolved between 358 and 541 MYA(Devonian–Cambrian).Divergence times for subphyla are generally between 358 and 485 MYA(Devonian–Ordovician),those of classes 145–358 MYA(Jurassic–Carboniferous),subclasses 66–358 MYA(Cretaceous–Carboniferous),orders 23–252 MYA(Paleogene–Triassic),families 2.8–145 MYA(Neogene–Cretaceous),and genera 2.8–66 MYA(Neogene–Paleogene).Thus,there are wide discrepancies in the times different taxa diverged.We provide an overview over Ascomycota,showing how application of temporal banding could affect the recognition of higher taxa at certain rank levels.We then use Sordariomycetes as an example where we use divergence times to provide additional evidence to stabilize ranking of taxa below class level.We propose a series of evolutionary periods that could be used as a guide to determine the various higher ranks of fungi:phyla[550 MYA,subphyla 400–550 MYA;classes 300–400 MYA;subclasses 250–300 MYA,orders 150–250 MYA,and families 50–150 MYA.It is proposed that classification schemes and ranking of taxa should,where possible,incorporate a polyphasic approach including phylogeny,phenotype,and estimate of divergence times.展开更多
Inaccurate taxonomic placement of fossils can lead to the accumulation of errors in molecular clock studies and their generated evolutionary lineages.There are limited fossil data that can be used in divergence time e...Inaccurate taxonomic placement of fossils can lead to the accumulation of errors in molecular clock studies and their generated evolutionary lineages.There are limited fossil data that can be used in divergence time estimations.Therefore,reliable morphological characterization and taxonomical identification of fossil fungi are extremely important.Most fossils of Dothideomycetes and Sordariomycetes are from the early Cenozoic(66-23 Mya),with fewer from the late Mesozoic(174-145 Mya).However,it is hard to distinguish some fossil descriptions as photographs and illustrations are unclear;thus,the validity of using these fossils in calibrations of molecular clocks is problematic.This study brings scattered paleobiological data on selected fossil Ascomycota,using descriptions,fossil images and illustrations,coupled with recent age estimations,and taxonomic and phylogenetic affinity of extant species.As an integrated approach,this study summarizes a historical fossil outline with a reliable minimum age for 16 calibrating points viz.crown of Aigialus,Anzia,Aspergillus,Asterina,Calicium chlorosporum–C.nobile,Capnodiales,Chaenotheca,Colletotrichum,Diaporthales,Meliola,Ophiocordyceps,Microthyriales,Microthyrium,Muyocopron,Pezizomycotina and Stigmatomyces.A scheme of Ascomycota ancient lineages is also provided in order to improve divergence time estimations.展开更多
Xylariomycetidae(Ascomycota)is a highly diversified group with variable stromatic characters.Our research focused on inconspicuous stromatic xylarialean taxa from China,Italy,Russia,Thailand and the United Kingdom.Det...Xylariomycetidae(Ascomycota)is a highly diversified group with variable stromatic characters.Our research focused on inconspicuous stromatic xylarialean taxa from China,Italy,Russia,Thailand and the United Kingdom.Detailed morpho-logical descriptions,illustrations and combined ITS-LSU-rpb2-tub2-tef1 phylogenies revealed 39 taxa from our collections belonging to Amphisphaeriales and Xylariales.A new family(Appendicosporaceae),five new genera(Magnostiolata,Mela-nostictus,Neoamphisphaeria,Nigropunctata and Paravamsapriya),27 new species(Acrocordiella photiniicola,Allocryp-tovalsa sichuanensis,Amphisphaeria parvispora,Anthostomella lamiacearum,Apiospora guiyangensis,A.sichuanensis,Biscogniauxia magna,Eutypa camelliae,Helicogermslita clypeata,Hypocopra zeae,Magnostiolata mucida,Melanostictus longiostiolatus,M.thailandicus,Nemania longipedicellata,N.delonicis,N.paraphysata,N.thailandensis,Neoamphispha-eria hyalinospora,Neoanthostomella bambusicola,Nigropunctata bambusicola,N.nigrocircularis,N.thailandica,Occul-titheca rosae,Paravamsapriya ostiolata,Peroneutypa leucaenae,Seiridium italicum and Vamsapriya mucosa)and seven new host/geographical records are introduced and reported.Divergence time estimates indicate that Delonicicolales diverged from Amphisphaeriales+Xylariales at 161(123-197)MYA.Amphisphaeriales and Xylariales diverged 154(117-190)MYA with a crown age of 127(92-165)MYA and 147(111-184)MYA,respectively.Appendicosporaceae(Amphisphaeriales)has a stem age of 89(65-117)MYA.Ancestral character state reconstruction indicates that astromatic,clypeate ascomata with aseptate,hyaline ascospores that lack germ slits may probably be ancestral Xylariomycetidae having plant-fungal endo-phytic associations.The Amphisphaeriales remained mostly astromatic with common septate,hyaline ascospores.Stromatic variations may have developed mostly during the Cretaceous period.Brown ascospores are common in Xylariales,but they first appeared in Amphisphaeriaceae,Melogrammataceae and Sporocadaceae during the early Cretaceous.The ascospore germ slits appeared only in Xylariales during the Cretaceous after the divergence of Lopadostomataceae.Hyaline,filiform and apiospores may have appeared as separate lineages,providing the basis for Xylariaceae,which may have diverged inde-pendently.The future classification of polyphyletic xylarialean taxa will not be based on stromatic variations,but the type of ring,the colour of the ascospores,and the presence or absence or the type of germ slit.展开更多
This article provides morphological descriptions and illustrations of microfungi associated with the invasive weed,Chro-molaena odorata,which were mainly collected in northern Thailand.Seventy-seven taxa distributed i...This article provides morphological descriptions and illustrations of microfungi associated with the invasive weed,Chro-molaena odorata,which were mainly collected in northern Thailand.Seventy-seven taxa distributed in ten orders,23 families(of which Neomassarinaceae is new),12 new genera(Chromolaenicola,Chromolaenomyces,Longiappendispora,Pseudocapulatispora,Murichromolaenicola,Neoophiobolus,Paraleptospora,Pseudoroussoella,Pseudostaurosphaeria,Pseudothyridariella,Setoarthopyrenia,Xenoroussoella),47 new species(Aplosporella chromolaenae,Arthrinium chromolae-nae,Chromolaenicola chiangraiensis,C.lampangensis,C.nanensis,C.thailandensis,Chromolaenomyces appendiculatus,Diaporthe chromolaenae,Didymella chromolaenae,Dyfrolomyces chromolaenae,Leptospora chromolaenae,L.phraeana,Longiappendispora chromolaenae,Memnoniella chromolaenae,Montagnula chiangraiensis,M.chromolaenae,M.chromo-laenicola,M.thailandica,Murichromolaenicola chiangraiensis,M.chromolaenae,Muyocopron chromolaenae,M.chromo-laenicola,Neomassarina chromolaenae,Neoophiobolus chromolaenae,Neopyrenochaeta chiangraiensis,N.chromolaenae,N.thailandica,N.triseptatispora,Nigrograna chromolaenae,Nothophoma chromolaenae,Paraleptospora chromolaenae,P.chromolaenicola,Patellaria chromolaenae,Pseudocapulatispora longiappendiculata,Pseudoroussoella chromolaenae,Pseudostaurosphaeria chromolaenae,P.chromolaenicola,Pseudothyridariella chromolaenae,Pyrenochaetopsis chromolae-nae,Rhytidhysteron chromolaenae,Setoarthopyrenia chromolaenae,Sphaeropsis chromolaenicola,Tremateia chiangraiensis,T.chromolaenae,T.thailandensis,Xenoroussoella triseptata,Yunnanensis chromolaenae),12 new host records,three new taxonomic combinations(Chromolaenicola siamensis,Pseudoroussoella elaeicola,Pseudothyridariella mahakashae),and two reference specimens(Torula chromolaenae,T.fici)are described and illustrated.Unlike some other hosts,e.g.bamboo(Poaceae)and Pandanaceae,the dominant group of fungi on Siam weed were Dothideomycetes.Only 15 species previously recorded from northern Thailand were found in this study.Most of the taxa are likely to have jumped hosts from surrounding plants and are unlikely to be a specialist to Siam weed.Most fungal families found on Siam weed had divergence estimates with stem ages in the Cretaceous,which coincided with the expected origin of the host family(Asteraceae).This further indicates that the species have jumped hosts,as it is unlikely that the taxa on the alien Siam weed came from the Americas with its host.They may,however,have jumped from other Asteraceae hosts.In a preliminary screening 40(65%)of the 62 species tested showed antimicrobial activity and thus,the fungi associated with C.odorata may be promising sources of novel bioactive compound discovery.We provide a checklist of fungi associated with C.odorata based on the USDA Systematic Mycology and Microbiology Laboratory(SMML)database,relevant literature and our study.In total,130 taxa(116 identified and 14 unidentified species)are distributed in 20 orders,48 families and 85 genera.Pseudocercospora is the most commonly encountered genus on Siam weed.展开更多
Species and generic recognition in the order Xylariales has been uncertain due to lack of molecular data from authentic cultures,as well as overlapping morphological characteristics.In this study,we revise the famili...Species and generic recognition in the order Xylariales has been uncertain due to lack of molecular data from authentic cultures,as well as overlapping morphological characteristics.In this study,we revise the families Graphostromataceae,Hypoxylaceae,Lopadostomataceae and Xylariaceae in Xylariales.Our study is based on DNA sequence data derived from living cultures of fresh isolates,data from GenBank and morphological observation of type and worldwide herbarium specimens.We also collected new specimens from Germany,Italy and Thailand.Combined analyses of ITS,LSU,RPB2 and b-tubulin sequence data were used to reconstruct the molecular phylogeny of the above families.Generic and familiar boundaries between these families are revised and presented in an updated combined phylogenetic tree.We accept six genera in Graphostromataceae,19 genera in Hypoxylaceae,four in Lopadostomataceae and 37 genera in Xylariaceae.Five genera previously treated in Xylariaceae are placed in Amphisphaeriales genera incertae sedis and seven genera are placed in Xylariales genera incertae sedis.Two genera are placed in Sordariomycetes genera incertae sedis,while four genera are placed as Xylariomycetidae genera incertae sedis.Three genera are considered as doubtful.Barrmaelia and Cannonia,presently included in Xylariaceae are transferred to Diatrypaceae and Coniochaetales respectively,based on their morphology and phylogeny.Areolospora and Myconeesia are excluded from Xylariaceae and synonymized with Phaeosporis and Anthostomella respectively.Updated descriptions and illustrations are provided for all taxa with notes provided on each genus.Excluded and doubtful genera are listed with notes on their taxonomy and phylogeny.Taxonomic keys are provided for all revised families with morphological details for genera within the families.展开更多
The cryptic lifestyle of most fungi necessitates molecular identification of the guild in environmental studies.Over the past decades,rapid development and affordability of molecular tools have tremendously improved i...The cryptic lifestyle of most fungi necessitates molecular identification of the guild in environmental studies.Over the past decades,rapid development and affordability of molecular tools have tremendously improved insights of the fungal diversity in all ecosystems and habitats.Yet,in spite of the progress of molecular methods,knowledge about functional properties of the fungal taxa is vague and interpretation of environmental studies in an ecologically meaningful manner remains challenging.In order to facilitate functional assignments and ecological interpretation of environmental studies we introduce a user friendly traits and character database FungalTraits operating at genus and species hypothesis levels.Combining the information from previous efforts such as FUNGuild and FunFun together with involvement of expert knowledge,we reannotated 10,210 and 151 fungal and Stramenopila genera,respectively.This resulted in a stand-alone spreadsheet dataset covering 17 lifestyle related traits of fungal and Stramenopila genera,designed for rapid functional assignments of environmental stud-ies.In order to assign the trait states to fungal species hypotheses,the scientific community of experts manually categorised and assigned available trait information to 697,413 fungal ITS sequences.On the basis of those sequences we were able to summarise trait and host information into 92,623 fungal species hypotheses at 1%dissimilarity threshold.展开更多
Molecular phylogenetic studies of cultures derived from some specimens of plant-inhabiting Sordariomycetes using ITS,LSU,rpb2 and tub2 DNA sequence data revealed close affinities to strains of Muscodor.The taxonomy of...Molecular phylogenetic studies of cultures derived from some specimens of plant-inhabiting Sordariomycetes using ITS,LSU,rpb2 and tub2 DNA sequence data revealed close affinities to strains of Muscodor.The taxonomy of this biotechnologi-cally important genus,which exclusively consists of endophytes with sterile mycelia that produce antibiotic volatile secondary metabolites,was based on a rather tentative taxonomic concept.Even though it was accommodated in Xylariaceae,its phylo-genetic position had so far remained obscure.Our phylogeny shows that Muscodor species have affinities to the xylarialean genera Emarcea and Induratia,which is corroborated by the fact that their sexual states produce characteristic apiospores.These data allow for the integration of Muscodor in Induratia,i.e.the genus that was historically described first.The multi-locus phylogenetic tree clearly revealed that a clade comprising Emarcea and Induratia forms a monophylum separate from representatives of Xylariaceae,for which we propose the new family Induratiaceae.Divergence time estimations revealed that Induratiaceae has been diverged from the Xylariaceae+Clypeosphaeriaceae clade at 93(69-119)million years ago(Mya)with the crown age of 61(39-85)Mya during the Cretaceous period.The ascospore-derived cultures were studied for the production of volatile metabolites,using both,dual cultures for assessment of antimicrobial effects and extensive analyses using gas chromatography coupled with mass spectrometry(GC-MS).The antimicrobial effects observed were significant,but not as strong as in the case of the previous reports on Muscodor species.The GC-MS results give rise to some doubt on the validity of the previous identification of certain volatiles.Many peaks in the GC-MS chromatograms could not be safely identified by database searches and may represent new natural products.The isolation of these compounds by preparative chromatography and their subsequent characterisation by nuclear magnetic resonance(NMR)spectroscopy or total synthesis will allow for a more concise identification of these volatiles,and they should also be checked for their individual contri-bution to the observed antibiotic effects.This will be an important prerequisite for the development of biocontrol strains.展开更多
Numerous new taxa and classifications of Dothideomycetes have been published following the last monograph of families of Dothideomycetes in 2013.A recent publication by Honsanan et al.in 2020 expanded information of f...Numerous new taxa and classifications of Dothideomycetes have been published following the last monograph of families of Dothideomycetes in 2013.A recent publication by Honsanan et al.in 2020 expanded information of families in Dothideo-mycetidae and Pleosporomycetidae with modern classifications.In this paper,we provide a refined updated document on orders and families incertae sedis of Dothideomycetes.Each family is provided with an updated description,notes,including figures to represent the morphology,a list of accepted genera,and economic and ecological significances.We also provide phylogenetic trees for each order.In this study,31 orders which consist 50 families are assigned as orders incertae sedis in Dothideomycetes,and 41 families are treated as families incertae sedis due to lack of molecular or morphological evidence.The new order,Catinellales,and four new families,Catinellaceae,Morenoinaceae Neobuelliellaceae and Thyrinulaceae are introduced.Seven genera(Neobuelliella,Pseudomicrothyrium,Flagellostrigula,Swinscowia,Macroconstrictolumina,Pseudobogoriella,and Schummia)are introduced.Seven new species(Acrospermum urticae,Bogoriella complexoluminata,Dothiorella ostryae,Dyfrolomyces distoseptatus,Macroconstrictolumina megalateralis,Patellaria microspora,and Pseu-domicrothyrium thailandicum)are introduced base on morphology and phylogeny,together with two new records/reports and five new collections from different families.Ninety new combinations are also provided in this paper.展开更多
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.Th...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 appres-soria 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.展开更多
This is a continuity of a series of taxonomic and phylogenetic papers on the fungi where materials were collected from many countries,examined and described.In addition to extensive morphological descriptions and appr...This is a continuity of a series of taxonomic and phylogenetic papers on the fungi where materials were collected from many countries,examined and described.In addition to extensive morphological descriptions and appropriate asexual and sexual connections,DNA sequence data are also analysed from concatenated datasets to infer phylogenetic relationships and substantiate systematic positions of taxa within appropriate ranks.Wherever new species or combinations are proposed,we apply an integrative approach using morphological and molecular data as well as ecological features wherever applicable.Notes on 112 fungal taxa are compiled in this paper including Biatriosporaceae and Roussoellaceae,Didysimulans gen.nov.,81 new species,18 new host records and new country records,five reference specimens,two new combinations,and three sexual and asexual morph reports.The new species are Amanita cornelii,A.emodotrygon,Angustimassarina alni,A.arezzoensis,A.italica,A.lonicerae,A.premilcurensis,Ascochyta italica,A.rosae,Austroboletus appendiculatus,Barriopsis thailandica,Berkleasmium ariense,Calophoma petasitis,Camarosporium laburnicola,C.moricola,C.grisea,C.ossea,C.paraincrustata,Colletotrichum sambucicola,Coprinopsis cerkezii,Cytospora gelida,Dacrymyces chiangraiensis,Didysimulans italica,D.mezzanensis,Entodesmium italica,Entoloma magnum,Evlachovaea indica,Exophiala italica,Favolus gracilisporus,Femsjonia monospora,Fomitopsis flabellata,F.roseoalba,Gongronella brasiliensis,Helvella crispoides,Hermatomyces chiangmaiensis,H.chromolaenae,Hysterium centramurum,Inflatispora caryotae,Inocybe brunneosquamulosa,I.luteobrunnea,I.rubrobrunnea,Keissleriella cirsii,Lepiota cylindrocystidia,L.flavocarpa,L.maerimensis,Lophiotrema guttulata,Marasmius luculentus,Morenoina calamicola,Moelleriella thanathonensis,Mucor stercorarius,Myrmecridium fluviae,Myrothecium septentrionale,Neosetophoma garethjonesii,Nigrograna cangshanensis,Nodulosphaeria guttulatum,N.multiseptata,N.sambuci,Panus subfasciatus,Paraleptosphaeria padi,Paraphaeosphaeria viciae,Parathyridaria robiniae,Penicillium punicae,Phaeosphaeria calamicola,Phaeosphaeriopsis yuccae,Pleurophoma italica,Polyporus brevibasidiosus,P.koreanus,P.orientivarius,P.parvovarius,P.subdictyopus,P.ulleungus,Pseudoasteromassaria spadicea,Rosellinia mearnsii,Rubroboletus demonensis,Russula yanheensis,Sigarispora muriformis,Sillia italica,Stagonosporopsis ailanthicola,Strobilomyces longistipitatus,Subplenodomus galicola and Wolfiporia pseudococos.The new combinations are Melanomma populina and Rubroboletus eastwoodiae.The reference specimens are Cookeina tricholoma,Gnomoniopsis sanguisorbae,Helvella costifera,Polythrincium trifolii and Russula virescens.The new host records and country records are Ascochyta medicaginicola,Boletellus emodensis,Cyptotrama asprata,Cytospora ceratosperma,Favolaschia auriscalpium,F.manipularis,Hysterobrevium mori,Lentinus sajor-caju,L.squarrosulus,L.velutinus,Leucocoprinus cretaceus,Lophiotrema vagabundum,Nothophoma quercina,Platystomum rosae,Pseudodidymosphaeria phlei,Tremella fuciformis,Truncatella spartii and Vaginatispora appendiculata and three sexual and asexual morphs are Aposphaeria corallinolutea, Dothiorabuxi and Hypocrella calendulina.展开更多
This paper provides illustrated descriptions of micro-fungi newly found on Pandanaceae in China and Thailand.The fungi are accommodated in 31 families.New taxa described include a new family,seven new genera,65 new sp...This paper provides illustrated descriptions of micro-fungi newly found on Pandanaceae in China and Thailand.The fungi are accommodated in 31 families.New taxa described include a new family,seven new genera,65 new species,16 previously known species.A new family:Malaysiascaceae(Glomerellales).New genera are Acremoniisimulans(Plec-tosphaerellaceae),Pandanaceomyces,Pseudoachroiostachy(Nectriaceae),Pseudohyaloseta(Niessliaceae),Pseudoor-natispora(Stachybotriaceae)and Yunnanomyces(Sympoventuriaceae).New species are Acremoniisimulans thailandensis,Beltrania krabiensis,Beltraniella pandanicola,B.thailandicus,Canalisporium krabiense,C.thailandensis,Clonostachys krabiensis,Curvularia chonburiensis,C.pandanicola,C.thailandicum,C.xishuangbannaensis,Cylindrocladiella xishuangbannaensis,Dictyochaeta pandanicola,Dictyocheirospora nabanheensis,D.pandanicola,D.xishuangbannaen-sis,Dictyosporium appendiculatum,Di.guttulatum,Di.hongkongensis,Di.krabiense,Di.pandanicola,Distoseptispora thailandica,D.xishuangbannaensis,Helicoma freycinetiae,Hermatomyces biconisporus,Lasiodiplodia chonburiensis,L.pandanicola,Lasionectria krabiense,Menisporopsis pandanicola,Montagnula krabiensis,Musicillium pandanicola,Neofusicoccum pandanicola,Neohelicomyces pandanicola,Neooccultibambusa thailandensis,Neopestalotiopsis chiang-maiensis,N.pandanicola,N.phangngaensis,Pandanaceomyces krabiensis,Paracylindrocarpon nabanheensis,P.pan-danicola,P.xishuangbannaensis,Parasarcopodium hongkongensis,Pestalotiopsis krabiensis,P.pandanicola,Polyplosphaeria nabanheensis,P.pandanicola,P.xishuangbannaensis,Pseudoachroiostachys krabiense,Pseu-doberkleasmium pandanicola,Pseudochaetosphaeronema pandanicola,Pseudohyaloseta pandanicola,Pseudoornatispora krabiense,Pseudopithomyces pandanicola,Rostriconidium pandanicola,Sirastachys phangngaensis,Stictis pandanicola,Terriera pandanicola,Thozetella pandanicola,Tubeufia freycinetiae,T.parvispora,T.pandanicola,Vermiculariopsiella hongkongensis,Volutella krabiense,V.thailandensis and Yunnanomyces pandanicola.Previous studies of micro-fungi on Pandanaceae have not included phylogenetic support.Inspiration for this study came from the book Fungi Associated with Pandanaceae by Whitton,McKenzie and Hyde in 2012.Both studies reveal that the micro-fungi on Pandanaceae is particularly rich in hyphomycetes.All data presented herein are based on morphological examination of specimens,coupled with phylogenetic sequence data to better integrate taxa into appropriate taxonomic ranks and infer their evolu-tionary relationships.展开更多
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 t...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 fore-most 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 differ-ent 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.展开更多
Knowledge of the relationships and thus the classification of fungi,has developed rapidly with increasingly widespread use of molecular techniques,over the past 10–15 years,and continues to accelerate.Several genera ...Knowledge of the relationships and thus the classification of fungi,has developed rapidly with increasingly widespread use of molecular techniques,over the past 10–15 years,and continues to accelerate.Several genera have been found to be polyphyletic,and their generic concepts have subsequently been emended.New names have thus been introduced for species which are phylogenetically distinct from the type species of particular genera.The ending of the separate naming of morphs of the same species in 2011,has also caused changes in fungal generic names.In order to facilitate access to all important changes,it was desirable to compile these in a single document.The present article provides a list of generic names of Ascomycota(approximately 6500 accepted names published to the end of 2016),including those which are lichen-forming.Notes and summaries of the changes since the last edition of‘Ainsworth&Bisby’s Dictionary of the Fungi’in 2008 are provided.The notes include the number of accepted species,classification,type species(with location of the type material),culture availability,life-styles,distribution,and selected publications that have appeared since 2008.This work is intended to provide the foundation for updating the ascomycete component of the"Without prejudice list of generic names of Fungi"published in 2013,which will be developed into a list of protected generic names.This will be subjected to the XIXth International Botanical Congress in Shenzhen in July 2017 agreeing to a modification in the rules relating to protected lists,and scrutiny by procedures determined by the Nomenclature Committee for Fungi(NCF).The previously invalidly published generic names Barriopsis,Collophora(as Collophorina),Cryomyces,Dematiopleospora,Heterospora(as Heterosporicola),Lithophila,Palmomyces(as Palmaria)and Saxomyces are validated,as are two previously invalid family names,Bartaliniaceae and Wiesneriomycetaceae.Four species of Lalaria,which were invalidly published are transferred to Taphrina and validated as new combinations.Catenomycopsis Tibell&Constant.is reduced under Chaenothecopsis Vain.,while Dichomera Cooke is reduced under Botryosphaeria Ces.&De Not.(Art.59).展开更多
This article is the 15th contribution in the Fungal Diversity Notes series,wherein 115 taxa from three phyla,nine classes,28 orders,48 families,and 64 genera are treated.Fungal taxa described and illustrated in the pr...This article is the 15th contribution in the Fungal Diversity Notes series,wherein 115 taxa from three phyla,nine classes,28 orders,48 families,and 64 genera are treated.Fungal taxa described and illustrated in the present study include a new family,five new genera,61 new species,five new combinations,one synonym,one new variety and 31 records on new hosts or new geographical distributions.Ageratinicolaceae fam.nov.is introduced and accommodated in Pleosporales.The new genera introduced in this study are Ageratinicola,Kevinia,Pseudomultiseptospora(Parabambusicolaceae),Marasmiellomycena,and Vizzinia(Porotheleaceae).Newly described species are Abrothallus altoandinus,Ageratinicola kunmingensis,Allocryptovalsa aceris,Allophoma yuccae,Apiospora cannae,A.elliptica,A.pallidesporae,Boeremia wisteriae,Calycina papaeana,Clypeo-coccum lichenostigmoides,Coniochaeta riskali-shoyakubovii,Cryphonectria kunmingensis,Diaporthe angustiapiculata,D.campylandrae,D.longipapillata,Diatrypella guangdongense,Dothiorella franceschinii,Endocalyx phoenicis,Epicoc-cum terminosporum,Fulvifomes karaiensis,F.pannaensis,Ganoderma ghatensis,Hysterobrevium baoshanense,Inocybe avellaneorosea,I.lucida,Jahnula oblonga,Kevinia lignicola,Kirschsteiniothelia guangdongensis,Laboulbenia caprina,L.clavulata,L.cobiae,L.cosmodisci,L.nilotica,L.omalii,L.robusta,L.similis,L.stigmatophora,Laccaria rubriporus,Lasiodiplodia morindae,Lyophyllum agnijum,Marasmiellomycena pseudoomphaliiformis,Melomastia beihaiensis,Nemania guangdongensis,Nigrograna thailandica,Nigrospora ficuum,Oxydothis chinensis,O.yunnanensis,Petriella thailandica,Phaeoacremonium chinensis,Phialocephala chinensis,Phytophthora debattistii,Polyplosphaeria nigrospora,Pronectria loweniae,Seriascoma acutispora,Setoseptoria bambusae,Stictis anomianthi,Tarzetta tibetensis,Tarzetta urceolata,Tetraploa obpyriformis,Trichoglossum beninense,and Tricoderma pyrrosiae.We provide an emendation for Urnula ailaoshanensis Agaricus duplocingulatoides var.brevisporus introduced as a new variety based on morphology and phylogeny.展开更多
Correction to:Fungal Diversity(2020)105:116 https://doi.org/10.1007/s13225-020-00466-2 There were errors in the name of author LászlóG.Nagy and in affiliation no.31 in the original publication.The original a...Correction to:Fungal Diversity(2020)105:116 https://doi.org/10.1007/s13225-020-00466-2 There were errors in the name of author LászlóG.Nagy and in affiliation no.31 in the original publication.The original article has been corrected.展开更多
基金provide by National Natural Science Foundation of China(Nos.32460002,31960005,32000009,32170019,NSFC 32260004)ussian Science Foundation(Nos.24-44-00099,23-74-00071,24-44-00099)+14 种基金National Research Council of Thailand(No.N42A650547)National Institute of Nursing Research(1P20GM152333-01)National Science Foundation(2029478)Japan Society for the Promotion of Science(JSPS,23K05900)National Science Foundation of China(32150410362)Croatian Science Foundation(HRZZIP-2022-10-5219)RSF(21-74-20089)ZIN RAS(122031100260-0)Science and Technology Human Resource Development Project(R3RJ2)Asian Development Bank,Conselho Naional de Desenvolvimento Científico e Tecnológico(306632/2022-5),zygosporic fungi in the Atlantic Forest of Pernambuco and Paraiba,Brazil(FACEPE–APQ-1346-2.12/22),Agriculture Sci-Tech Renovation(XJNKYWDZC–2022004)Research Foundation—Flanders(1206024N),FWF(P31038)Talent Recruitment Plan of Yunnan Province“High-End Foreign Experts,National Centre for Research and Development,Poland”(Tango-IV-C/0005/2019)CAS President’s International Fellowship Initiative(2021FYB0005)Smart Yunnan Project(E13K281261)High-Level Talent Recruitment Plan of Yunnan Provinces.
文摘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.
基金provide by National Natural Science Foundation of China(Nos.32460002,31960005,32000009,32170019,NSFC 32260004)Russian Science Foundation(Nos.24-44-00099,23-74-00071,24-44-00099)+17 种基金National Research Council of Thailand(No.N42A650547)National Institute of Nursing Research(1P20GM152333-01)National Science Foundation(2029478)Japan Society for the Promotion of Science(JSPS,23K05900)National Science Foundation of China(32150410362)Croatian Science Foundation(HRZZ-IP-2022-10-5219)RSF(21-74-20089)ZIN RAS(122031100260-0)Science and Technology Human Resource Development Project(R3RJ2)Asian Development Bank,Conselho Naional de Desenvolvimento Científico e Tecnológico(306632/2022-5)zygosporic fungi in the Atlantic Forest of Pernambuco and Paraíba,Brazil(FACEPE-APQ-1346-2.12/22)Agriculture Sci-Tech Renovation(XJNKYWDZC-2022004)Research Foundation-Flanders(1206024N)FWF(P31038)Talent Recruitment Plan of Yunnan Province“High-End Foreign Experts”,National Centre for Research and Development,Poland(Tango-Ⅳ-C/0005/2019)CAS President’s International Fellowship Initiative(2021FYB0005)Smart Yunnan Project(E13K281261)High-Level Talent Recruitment Plan of Yunnan Provinces.
文摘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,Neocal-limastigomycota,Olpidiomycota,Rozellomycota,Sanchytriomycota,and Zoopagomycota.In the phylogenies,Caulochy-triomycota 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.
基金K.D.Hyde thanks the Chinese Academy of Sciences,Project Number 2013T2S0030for the award of Visiting Professorship for Senior International Scientists at Kunming Institute of Botany.The authors extend their appreciation to the International Scientific Partnership Program ISPP at King Saud University for funding this research work through ISPP#0089+2 种基金K.D.Hyde would like to thank the Thailand Research Fund(TRF)Grant No.RSA5980068 entitled Biodiversityphylogeny and role of fungal endophytes on above parts of Rhizophora apiculata and Nypa fruticans and National Research Council of Thailand(NRCT)entitled Diseases of mangrove trees and maintenance of good forestry practice(Grant Number:60201000201)The authors would like to thank NRCT for the grant to study the Biodiversity,phylogeny and role of fungal endophytes of Pandanaceae(Grant No.:592010200112).
文摘The previous phylogenies of Sordariomycetes by M.E.Barr,O.E.Eriksson and D.L.Hawksworth,and T.Lumbsch and S.Huhndorf,were mainly based on morphology and thus were somewhat subjective.Later outlines by T.Lumbsch and S.Huhndorf,and Maharachchikumbura and co-authors,took into account phylogenetic evidence.However,even these phylogenetic driven arrangements for Sordariomycetes,were somewhat subjective,as the arrangements in trees depended on many variables,such as number of taxa,different gene regions and methods used in the analyses.What is needed is extra evidence to help standardize ranking in the fungi.Estimation of divergence times using molecular clock methods has been proposed for providing additional rational for higher ranking of taxa.Thus,in Sordariomycetes,a divergence period(i.e.200–300 MYA)can be used as criteria to judge when a group of related taxa evolved and what rank they should be given.In this paper,we provide an updated classification of accepted subclasses,orders of Sordariomycetes and use divergence times to provide additional evidence to stabilize ranking of taxa in the class.We point out and discuss discrepancies where the phylogenetic tree conflicts with the molecular clock.
基金CAS President’s International Fellowship Initiative(PIFI)for Young Staff 2019-2021(grant number 2019FY0003)the Research Fund from China Postdoctoral Science Foundation(Grant No.Y71B283261)+45 种基金the Yunnan Provincial Department of Human Resources and Social Security(Grant No.Y836181261)National Science Foundation of China(NSFC)project code 31850410489 for financial research supportthe Foreign Experts Bureau of Yunnan Province,Foreign Talents Program(2018,Grant No.YNZ2018002)Thailand Research grants entitled Biodiversity,phylogeny and role of fungal endophytes on above parts of Rhizophora apiculata and Nypa fruticans(Grant No:RSA5980068)the future of specialist fungi in a changing climate:baseline data for generalist and specialist fungi associated with ants,Rhododendron species and Dracaena species(Grant No:DBG6080013)Impact of climate change on fungal diversity and biogeography in the Greater Mekong Subregion(Grant No:RDG6130001)the Key Research Program of Frontier Sciences of the Chinese Academy of Sciences(Grant No.QYZDY-SSW-SMC014)the National Science Foundation of China and the Chinese Academy of Sciences for financial support under the following grants:41761144055,41771063 and Y4ZK111B01the Fonds de la Recherche Scientifique-FNRS(Belgium)for travel grantsCAS President’s International Fellowship Initiative(PIFI)for funding his postdoctoral research(Grant No.2018PC0006)the National Science Foundation of China(NSFC,project code 31750110478)CAS President’s International Fellowship Initiative(PIFI)for funding his postdoctoral research(Grant No.2019PC0008)supported under the Distinguished Scientist Fellowship Program(DSFP),King Saud University,Kingdom of Saudi Arabia.the Kerala State Council for Science,Technology and Environment(KSCSTE)in the form of a PhD fellowship(Grant No.001/FSHP/2011/CSTE)the Principal Chief Conservator of forests,Kerala State,for granting permission(No.WL10-4937/2012,dated 03-10-2013)to collect agarics from the forests of Keralathe Council of Scientific&Industrial Research(CSIR),New Delhi,India,in the form of an award of CSIR Research Associateship(09/043(0178)2K17 dated:31/03/2017)the National Natural Science Foundation of China(Project ID:31470152 and 31360014)the Foundation of Innovative Group of Edible Mushrooms Industry of Beijing(Project ID:BAIC05-2017)the 5th batch of Postdoctoral Orientation Training Personnel in Yunnan Province and the 64th batch of China Postdoctoral Science FoundationCNPq for the Ph.D scholarship of RLMA(140283/2016-1)Pos-Graduacao em Biologia de Fungos(UFPE,Brazil)Capes(Capes-SIU 008/13)CNPq(PQ 307601/2015-3)FACEPE(APQ 0375-2.03/15)for funding the researchfinancial support from the Agreement ENDESA and San Ignacio de Huinay Foundations and Consejo Superior de Investigaciones Cientificas,CSIC(Projects No.2011HUIN10,2013CL0012,2014CL0011)the AECID(Agencia Espanola de Cooperacion Internacional para el Desarrollo)and Plan Nacional I+D+i project no.CGL2015-67459-Psupported by a Predoctoral Grant from the Ministerio de Economıa y Competitividad(Spain)(BES-2016-077793)Croatian Science Foundation for their partial support under the project HRZZ-IP-2018-01-1736(ForFungiDNA)supported by the Graduate Program for the Undiscovered Taxa of Koreathe Project on Survey and Discovery of Indigenous Fungal Species of Korea funded by NIBR and Project on Discovery of Fungi from Freshwater and Collection of Fungarium funded by NNIBR of the Ministry of Environment(MOE)in part carried out with the support of Cooperative Research Program for Agriculture Science and Technology Development(PJ013744)Rural Development Administration,and BK21 PLUS program funded by Ministry of Education,Republic of Koreathe CASTWAS for the PhD Fellowship.Sanjay K.Singh,Paras Nath Singh,Shiwali Rana and Frank Kwekucher Ackah thank Director,MACS,Agharkar Research Institute,Pune,India for providing facilities.Shiwali Rana and Frank Kwekucher Ackah thank UGC(Junior Research Fellowship)and DST,Govt.of India(CV Raman Fellowship for African Researchers),respectively.Gen-Nuo Wang,Huang Zhang,Wei Dong and Xian-Dong Yu thank the National Natural Science Foundation of China(Project ID:NSF 31500017).Bandarupalli Devadatha and V.Venkateswara Sarma thank The Ministry of Earth sciences,Govt.of India(Sanction order:MOES/36/OO1S/Extra/40/2014/PC-IV dt.14.1.2015)for a funding of the project,T,District Forest Office,Tiruvarur,Tamil Nadu and PCCF(Head of Forest Force),Chennai,Tamil Nadu Forest Department for providing permission to collect samples from Muthupet mangroves,and Department of Biotechnology,Pondicherry University is thanked for providing the facilities.Myung Soo Park,Seung-Yoon Oh and Young Woon Lim thank the Marine Bio Resource Bank Program of the Ministry of Ocean&Fisheries,Korea.Olinto Pereira thanks the CAPES,CNPq and FAPEMIG for financial support.Neven Matocˇec,Ivana Kusˇan and Margita Jadan express their gratitude to Livio Lorenzon,Enrico Bizio and Raffaella Trabucco(MCVE)for their kind help with loan of Sarcopeziza sicula type materialparts of their research were financed by Public Institutions Sjeverni Velebit National Park and Paklenica National Parkthe National Natural Science Foundation of China(No.NSFC 31760013,NSFC 31260087,NSFC 31460561)the Scientific Research Foundation of Yunnan Provincial Department of Education(2017ZZX186)utilization of endophytes and the Thousand Talents Plan,Youth Project of Yunnan Provincesthe National Natural Science Foundation of China(No.31760014)and the Science and Technology Foundation of Guizhou Province(No.[2017]5788)Thailand Research Fund(TRF)Grant No MRG6080089 for financial research supportThe Royal Golden Jubilee Ph.D.Program(PHD60K0147)under Thailand Research Fund,for financial research supports on project entitle"Fungi on limestone outcrops from southern Thailand to lower himalyas"the National Research Council of Thailand(Grant No.61215320023,61215320013)the Thailand Research Fund(Grant No.TRG6180001)for research financial supportthe Thailand Research Fund(RTA 5880006)Chiang Mai University for partially support this research workChina-Thailand Joint Lab on Microbial Biotechnology(Most KY201701011)for financial supportthe Mushroom Research Foundation for research financial support and PhD Fellowships.
文摘This article is the ninth in the series of Fungal Diversity Notes,where 107 taxa distributed in three phyla,nine classes,31 orders and 57 families are described and illustrated.Taxa described in the present study include 12 new genera,74 new species,three new combinations,two reference specimens,a re-circumscription of the epitype,and 15 records of sexualasexual morph connections,new hosts and new geographical distributions.Twelve new genera comprise Brunneofusispora,Brunneomurispora,Liua,Lonicericola,Neoeutypella,Paratrimmatostroma,Parazalerion,Proliferophorum,Pseudoastrosphaeriellopsis,Septomelanconiella,Velebitea and Vicosamyces.Seventy-four new species are Agaricus memnonius,A.langensis,Aleurodiscus patagonicus,Amanita flavoalba,A.subtropicana,Amphisphaeria mangrovei,Baorangia major,Bartalinia kunmingensis,Brunneofusispora sinensis,Brunneomurispora lonicerae,Capronia camelliaeyunnanensis,Clavulina thindii,Coniochaeta simbalensis,Conlarium thailandense,Coprinus trigonosporus,Liua muriformis,Cyphellophora filicis,Cytospora ulmicola,Dacrymyces invisibilis,Dictyocheirospora metroxylonis,Distoseptispora thysanolaenae,Emericellopsis koreana,Galiicola baoshanensis,Hygrocybe lucida,Hypoxylon teeravasati,Hyweljonesia indica,Keissleriella caraganae,Lactarius olivaceopallidus,Lactifluus midnapurensis,Lembosia brigadeirensis,Leptosphaeria urticae,Lonicericola hyaloseptispora,Lophiotrema mucilaginosis,Marasmiellus bicoloripes,Marasmius indojasminodorus,Micropeltis phetchaburiensis,Mucor orantomantidis,Murilentithecium lonicerae,Neobambusicola brunnea,Neoeutypella baoshanensis,Neoroussoella heveae,Neosetophoma lonicerae,Ophiobolus malleolus,Parabambusicola thysanolaenae,Paratrimmatostroma kunmingensis,Parazalerion indica,Penicillium dokdoense,Peroneutypa mangrovei,Phaeosphaeria cycadis,Phanerochaete australosanguinea,Plectosphaerella kunmingensis,Plenodomus artemisiae,P.lijiangensis,Proliferophorum thailandicum,Pseudoastrosphaeriellopsis kaveriana,Pseudohelicomyces menglunicus,Pseudoplagiostoma mangiferae,Robillarda mangiferae,Roussoella elaeicola,Russula choptae,R.uttarakhandia,Septomelanconiella thailandica,Spencermartinsia acericola,Sphaerellopsis isthmospora,Thozetella lithocarpi,Trechispora echinospora,Tremellochaete atlantica,Trichoderma koreanum,T.pinicola,T.rugulosum,Velebitea chrysotexta,Vicosamyces venturisporus,Wojnowiciella kunmingensis and Zopfiella indica.Three new combinations are Baorangia rufomaculata,Lanmaoa pallidorosea and Wojnowiciella rosicola.The reference specimens of Canalisporium kenyense and Tamsiniella labiosa are designated.The epitype of Sarcopeziza sicula is re-circumscribed based on cyto-and histochemical analyses.The sexual-asexual morph connection of Plenodomus sinensis is reported from ferns and Cirsium for the first time.In addition,the new host records and country records are Amanita altipes,A.melleialba,Amarenomyces dactylidis,Chaetosphaeria panamensis,Coniella vitis,Coprinopsis kubickae,Dothiorella sarmentorum,Leptobacillium leptobactrum var.calidus,Muyocopron lithocarpi,Neoroussoella solani,Periconia cortaderiae,Phragmocamarosporium hederae,Sphaerellopsis paraphysata and Sphaeropsis eucalypticola.
基金the Foreign Experts Bureau of Yunnan Province,Foreign Talents Program(2018,Grant No.YNZ2018002)Thailand Research grants entitled Biodiversity,phylogeny and role of fungal endophytes on above parts of Rhizophora apiculata and Nypa fruticans(Grant No.RSA5980068)+60 种基金the future of specialist fungi in a changing climate:baseline data for generalist and specialist fungi associated with ants,Rhododendron species and Dracaena species(Grant No.DBG6080013)Impact of climate change on fungal diversity and biogeography in the Greater Mekong Subregion(Grant No.RDG6130001)Chiang Mai University for the award of visiting ProfessorCAS President’s International Fellowship Initiative(PIFI)for funding his postdoctoral research(Grant No.2018PC0006)the National Science Foundation of China(NSFC,project code 31750110478)supported by the Graduate Program for the Undiscovered Taxa of Koreain part by the Project on Survey and Discovery of Indigenous Fungal Species of Korea funded by NIBR and Project on Discovery of Fungi from Freshwater and Collection of Fungarium funded by NNIBR of the Ministry of Environment(MOE)in part carried out with the support of Cooperative Research Program for Agriculture Science and Technology Development(PJ013744),Rural Development Administration,Republic of Koreain part supported by the BK21 plus program through the National Research Foundation(NRF)funded by the Ministry of Education of Korea.Jian-Kui Liu thanks the National Natural Science Foundation of China(NSFC 31600032)the CNPq(Conselho Nacional de Desenvolvimento Cientifico e Tecnologico)for a research grant(309058/2015-5)funding for collecting trips(401186/2014-8)a collaborative project with RL as Special Visiting Professor(314570/2014-4)Funding for phylogenetic work on Graphidaceae was provided by a grant from the National Science Foundation(NSF)to The Field Museum:DEB-1025861"ATM-Assembling a taxonomic monograph:The lichen family Graphidaceae"PI Thorsten Lumbsch,CoPI Robert Luckingthe CAPES,CNPq,and FAPEMIG for financial support and ICMBio/FLONA-Paraopeba for providing facilities and permits for the exploration surveys of the mycodiversity in their protected areasthe Graduate Program for the Biodiversity and Biotechnology Network of the Legal Amazon(UFPA-MPEG,Brazil)the Conselho Nacional de Desenvolvimento Cientifico Programa de Capacitacao for the scholarship to AMSS(Programa de Capacitacao Institucional 303073/2018-7)CNPq(Sisbiota 563342/2010-2,PROTAX 562106/2010-3)FACEPE(APQ 0788-2.03/12)for funding this researchsupport by a long-term research development project No.RVO 67985939 of the Czech Academy of Sciences,Institute of Botanyfinancial support from Conselho Nacional de Pesquisa e Desenvolvimento Cientifico(CNPq)National Natural Science Foundation of China(Project IDs GJL:31500013,RLZ:31470152 and 31360014)for financial supportjoint project of the Charles Darwin Foundation(CDF)and the Galapagos National Park(DPNG),part of a national biodiversity assessment"Biodiversidad Genetica del Ecuador"led by the Instituto Nacional de Biodiversidad del Ecuador(INABIO)Thailand Research Fund(TRF)Grant No.MRG6080089 entitledTaxonomy and phylogeny of foliar fungi from Mangrove and to Dr.Putarak Chomnuntithe Thailand Research Fund(No.TRG6180001)the National Research Council of Thailand(No.61215320023)Plant Genetic Conservation Project under the Royal Initiation of Her Royal Highness Princess Maha Chakri Sirindhorn-Mae Fah Luang Universitygrateful to Croatian Science Foundation for their financial support under the project HRZZ-IP-2018-01-1736(For-FungiDNA)the Royal Golden Jubilee PhD Program under Thailand Research Fund(RGJ)for a personal grant to C.Phukhamsakda(The scholarship no.PHD/0020/2557 to study towards a PhD)China-Thailand Joint Lab on Microbial Biotechnology(Most KY201701011)for financial supportCAS President’s International Fellowship Initiative(PIFI)for young staff(Grant No.2019FYC0003)the Research Fund from China Postdoctoral Science Foundation(Grant No.Y71B283261)the Yunnan Provincial Department of Human Resources and Social Security(Grant No.Y836181261)National Science Foundation of China(NSFC)project code 31850410489 for financial supportthe National Research Council of Thailand(Grant No.256108A3070006)for financial supportthe National Natural Science Foundation of China(No.31760014)the Science and Technology Foundation of Guizhou Province(No.[2016]2863)partially supported by Chiang Mai Universitythe Graduate Program for the Biodiversity and Biotechnology Network of the Legal Amazon(UFPA-MPEG),the Museu Paraense Emilio Goeldi(MPEG),the Universidade do Estado do Amapa and the Universidade Federal de Pernambuco for the logistical support of their laboratories and herbariaCNPq for the scholarship of AMSS(Programa de Capacitacao Institucional 303073/2018-7)CNPq(Sisbiota 563342/2010-2,PROTAX 562106/2010-3)and FACEPE(APQ 0788-2.03/12)for funding this researchthe ATM of the Paris'Museum and"l'Institut Ecologie et Environnement"(CNRS-INEE)for funding the field trip with Shelly Masi to Africaall the practical help and sharing her experiencemade possible through research permit 034/MENESR/DIRCAB/DGESRSTI/DRSTSPI/SSSTI/16 from the"Ministere de l'education nationale,de l’enseignement superieur et de la recherche scientifique"of the Central African Republicfinanced in part by the National Geographic Society(grants 6365-98,7921-05)in more recent years by the ATM-project"Past and present biodiversity"of the Museum national d’histoire naturelle(Dirs.Ph.Janvier and S.Peigne)University of Mauritius for research supportthe Thailand Research Fund(PHD60K0147)contribution number 2248 of the Charles Darwin Foundation for the Galapagos IslandsLakmali Dissanayake and Binu Samarakoon for their supportCAS President’s International Fellowship Initiative(PIFI)for funding his postdoctoral research(Number 2019PC0008)the National Science Foundation of China and the Chinese Academy of Sciences for financial support under the following grants:41761144055,41771063 and Y4ZK111B01CAS President’s International Fellowship Initiative(Grant No.2018VBB0021)German Academic Exchange Service Fellowship(Grant No.57314018)Ministry of innovative development of the Republic of Uzbekistan(Projects No.P3-2014-0830174425 and PP-20170921183)for funding his research projectsthe 5th batch of Postdoctoral Orientation Training Personnel in Yunnan Province(Grant No.Y934283261)the 64th batch of China Postdoctoral Science Foundation(Grant No.Y913082271)their kind support on manuscript writing.Jianchu Xu thanks Key Research Program of Frontier Sciences"Response of Asian mountain ecosystems to global change",CAS(Grant No.QYZDYSSW-SMC014)the 64th batch of China Postdoctoral Science Foundation(Grant No.Y913083271)the support from UID/MULTI/04046/2019 Research Unit grant from FCT,Portugal to BioISI.
文摘This article is the tenth series of the Fungal Diversity Notes,where 114 taxa distributed in three phyla,ten classes,30 orders and 53 families are described and illustrated.Taxa described in the present study include one new family(viz.Pseudoberkleasmiaceae in Dothideomycetes),five new genera(Caatingomyces,Cryptoschizotrema,Neoacladium,Paramassaria and Trochilispora)and 71 new species,(viz.Acrogenospora thailandica,Amniculicola aquatica,A.guttulata,Angustimassarina sylvatica,Blackwellomyces lateris,Boubovia gelatinosa,Buellia viridula,Caatingomyces brasiliensis,Calophoma humuli,Camarosporidiella mori,Canalisporium dehongense,Cantharellus brunneopallidus,C.griseotinctus,Castanediella meliponae,Coprinopsis psammophila,Cordyceps succavus,Cortinarius minusculus,C.subscotoides,Diaporthe italiana,D.rumicicola,Diatrypella delonicis,Dictyocheirospora aquadulcis,D.taiwanense,Digitodesmium chiangmaiense,Distoseptispora dehongensis,D.palmarum,Dothiorella styphnolobii,Ellisembia aurea,Falciformispora aquatic,Fomitiporia carpinea,F.lagerstroemiae,Grammothele aurantiaca,G.micropora,Hermatomyces bauhiniae,Jahnula queenslandica,Kamalomyces mangrovei,Lecidella yunnanensis,Micarea squamulosa,Muriphaeosphaeria angustifoliae,Neoacladium indicum,Neodidymelliopsis sambuci,Neosetophoma miscanthi,N.salicis,Nodulosphaeria aquilegiae,N.thalictri,Paramassaria samaneae,Penicillium circulare,P.geumsanense,P.mali-pumilae,P.psychrotrophicum,P.wandoense,Phaeoisaria siamensis,Phaeopoacea asparagicola,Phaeosphaeria penniseti,Plectocarpon galapagoense,Porina sorediata,Pseudoberkleasmium chiangmaiense,Pyrenochaetopsis sinensis,Rhizophydium koreanum,Russula prasina,Sporoschisma chiangraiense,Stigmatomyces chamaemyiae,S.cocksii,S.papei,S.tschirnhausii,S.vikhrevii,Thysanorea uniseptata,Torula breviconidiophora,T.polyseptata,Trochilispora schefflerae and Vaginatispora palmae).Further,twelve new combinations(viz.Cryptoschizotrema cryptotrema,Prolixandromyces australi,P.elongatus,P.falcatus,P.longispinae,P.microveliae,P.neoalardi,P.polhemorum,P.protuberans,P.pseudoveliae,P.tenuistipitis and P.umbonatus),an epitype is chosen for Cantharellus goossensiae,a reference specimen for Acrogenospora sphaerocephala and new synonym Prolixandromyces are designated.Twenty-four new records on new hosts and new geographical distributions are also reported(i.e.Acrostalagmus annulatus,Cantharellus goossensiae,Coprinopsis villosa,Dothiorella plurivora,Dothiorella rhamni,Dothiorella symphoricarposicola,Dictyocheirospora rotunda,Fasciatispora arengae,Grammothele brasiliensis,Lasiodiplodia iraniensis,Lembosia xyliae,Morenoina palmicola,Murispora cicognanii,Neodidymelliopsis farokhinejadii,Neolinocarpon rachidis,Nothophoma quercina,Peroneutypa scoparia,Pestalotiopsis aggestorum,Pilidium concavum,Plagiostoma salicellum,Protofenestella ulmi,Sarocladium kiliense,Tetraploa nagasakiensis and Vaginatispora armatispora).
基金The authors extend their appreciation to the International Scientific Partnership Program ISPP at King Saud University for funding this research work through ISPP#0089.J.C.Xu extend his appreciation to the Key Research Program of Frontier Sciences of the Chinese Academy of Sciences,Project No.QYZDYSSW-SMC014for funding this work.K.D.Hyde extends his appreciation to the Chinese Academy of Sciences,Project No.2013T2S0030+3 种基金for the award of Visiting Professorship for Senior International Scientists at Kunming Institute of Botany and the Thailand Research Fund(TRF)Grant No.RSA5980068 entitled Biodiversity,phylogeny and role of fungal endophytes on above parts of Rhizophora apiculata and Nypa fruticans and National Research Council of Thailand(NRCT)for a grant entitled Diseases of mangrove trees and maintenance of good forestry practice(Grant No.:60201000201)The authors would also like to thank the National Natural Science Foundation of China to RLZ(Project IDs 31470152 and 31360014)NRCT Grant,Biodiversity,phylogeny and role of fungal endophytes of Pandanaceae(Grant No.:592010200112)K.D.Hyde.Patricia Wiltshire is thanked for providing details on the life and work of Dr Hawksworth.
文摘The history of assigning ranks to fungi,as well as the relative importance of using divergence time estimates is reviewed.The paper pays tribute to the major mycological players,and especially to David Hawksworth on his 70th birthday and his contribution to fungal ranking in Systema Ascomycetum from 1982 to 1998.Following the conclusion of the latter series,the ranking continued with the Outlines of Ascomycota in 2007 and 2010 and more recently with specific classes in‘Towards an outline of Sordariomycetes’and‘Families of Dothideomycetes’.Earlier classifications based on phenotype were certainly more subjective;however,remarkably many of these old arrangements have stood the test of time.More recently,phylogenetic analyses have provided evidence towards a natural classification,resulting in significant changes in many lineages.The classification arrangements however,are still subjective and dependent on the taxa analysed,resulting in different taxonomic interpretations and schemes,particularly when it comes to ranking.Thus,what have been considered as genera by some,have been introduced as families by others.More recently,estimation of divergence times using molecular clock methods have been used as objective evidence for higher ranking of taxa.A divergence period(i.e.200–300 MYA)can be used as a criterion to infer when a group of related taxa evolved and what rank they should be given.We compiled data on divergence times for various higher ranking taxa in the Kingdom Fungi.The kingdom evolved 1000–1600 MYA(Stenian–Calymmian),while the presently accepted phyla evolved between 358 and 541 MYA(Devonian–Cambrian).Divergence times for subphyla are generally between 358 and 485 MYA(Devonian–Ordovician),those of classes 145–358 MYA(Jurassic–Carboniferous),subclasses 66–358 MYA(Cretaceous–Carboniferous),orders 23–252 MYA(Paleogene–Triassic),families 2.8–145 MYA(Neogene–Cretaceous),and genera 2.8–66 MYA(Neogene–Paleogene).Thus,there are wide discrepancies in the times different taxa diverged.We provide an overview over Ascomycota,showing how application of temporal banding could affect the recognition of higher taxa at certain rank levels.We then use Sordariomycetes as an example where we use divergence times to provide additional evidence to stabilize ranking of taxa below class level.We propose a series of evolutionary periods that could be used as a guide to determine the various higher ranks of fungi:phyla[550 MYA,subphyla 400–550 MYA;classes 300–400 MYA;subclasses 250–300 MYA,orders 150–250 MYA,and families 50–150 MYA.It is proposed that classification schemes and ranking of taxa should,where possible,incorporate a polyphasic approach including phylogeny,phenotype,and estimate of divergence times.
基金The National Natural Science Foundation of China(NSFC 31600032)is acknowledged for funding this research workthe Mushroom Research Foundation(MRF),Chiang Mai,Thailand for providing a Postgraduate Scholarship+2 种基金the Grants entitled"The future of specialist fungi in a changing climate:baseline data for generalist and specialist fungi associated with ants,Rhododendron species and Dracaena species"(Grant No:DBG6080013)"Impact of climate change on fungal diversity and biogeography in the Greater Mekong Subregion"(Grant No:RDG6130001)for supporting this studypartially supported by Chiang Mai University.
文摘Inaccurate taxonomic placement of fossils can lead to the accumulation of errors in molecular clock studies and their generated evolutionary lineages.There are limited fossil data that can be used in divergence time estimations.Therefore,reliable morphological characterization and taxonomical identification of fossil fungi are extremely important.Most fossils of Dothideomycetes and Sordariomycetes are from the early Cenozoic(66-23 Mya),with fewer from the late Mesozoic(174-145 Mya).However,it is hard to distinguish some fossil descriptions as photographs and illustrations are unclear;thus,the validity of using these fossils in calibrations of molecular clocks is problematic.This study brings scattered paleobiological data on selected fossil Ascomycota,using descriptions,fossil images and illustrations,coupled with recent age estimations,and taxonomic and phylogenetic affinity of extant species.As an integrated approach,this study summarizes a historical fossil outline with a reliable minimum age for 16 calibrating points viz.crown of Aigialus,Anzia,Aspergillus,Asterina,Calicium chlorosporum–C.nobile,Capnodiales,Chaenotheca,Colletotrichum,Diaporthales,Meliola,Ophiocordyceps,Microthyriales,Microthyrium,Muyocopron,Pezizomycotina and Stigmatomyces.A scheme of Ascomycota ancient lineages is also provided in order to improve divergence time estimations.
基金Joint Fund of the National Natural Science Foundation of China and the Karst Science Research Center of Guizhou province,U1812401,Jian-Kui Jack LiuThailand Research,RDG6130001,Kevin D.Hyde+1 种基金Thailand Science Research and Innovation(TSRI)grant,DBG6280009,Kevin D.Hydethe State Research Task of the Subtropical Scientific Centre of the Russian Academy of Sciences(Theme No.0492-2021-0007).
文摘Xylariomycetidae(Ascomycota)is a highly diversified group with variable stromatic characters.Our research focused on inconspicuous stromatic xylarialean taxa from China,Italy,Russia,Thailand and the United Kingdom.Detailed morpho-logical descriptions,illustrations and combined ITS-LSU-rpb2-tub2-tef1 phylogenies revealed 39 taxa from our collections belonging to Amphisphaeriales and Xylariales.A new family(Appendicosporaceae),five new genera(Magnostiolata,Mela-nostictus,Neoamphisphaeria,Nigropunctata and Paravamsapriya),27 new species(Acrocordiella photiniicola,Allocryp-tovalsa sichuanensis,Amphisphaeria parvispora,Anthostomella lamiacearum,Apiospora guiyangensis,A.sichuanensis,Biscogniauxia magna,Eutypa camelliae,Helicogermslita clypeata,Hypocopra zeae,Magnostiolata mucida,Melanostictus longiostiolatus,M.thailandicus,Nemania longipedicellata,N.delonicis,N.paraphysata,N.thailandensis,Neoamphispha-eria hyalinospora,Neoanthostomella bambusicola,Nigropunctata bambusicola,N.nigrocircularis,N.thailandica,Occul-titheca rosae,Paravamsapriya ostiolata,Peroneutypa leucaenae,Seiridium italicum and Vamsapriya mucosa)and seven new host/geographical records are introduced and reported.Divergence time estimates indicate that Delonicicolales diverged from Amphisphaeriales+Xylariales at 161(123-197)MYA.Amphisphaeriales and Xylariales diverged 154(117-190)MYA with a crown age of 127(92-165)MYA and 147(111-184)MYA,respectively.Appendicosporaceae(Amphisphaeriales)has a stem age of 89(65-117)MYA.Ancestral character state reconstruction indicates that astromatic,clypeate ascomata with aseptate,hyaline ascospores that lack germ slits may probably be ancestral Xylariomycetidae having plant-fungal endo-phytic associations.The Amphisphaeriales remained mostly astromatic with common septate,hyaline ascospores.Stromatic variations may have developed mostly during the Cretaceous period.Brown ascospores are common in Xylariales,but they first appeared in Amphisphaeriaceae,Melogrammataceae and Sporocadaceae during the early Cretaceous.The ascospore germ slits appeared only in Xylariales during the Cretaceous after the divergence of Lopadostomataceae.Hyaline,filiform and apiospores may have appeared as separate lineages,providing the basis for Xylariaceae,which may have diverged inde-pendently.The future classification of polyphyletic xylarialean taxa will not be based on stromatic variations,but the type of ring,the colour of the ascospores,and the presence or absence or the type of germ slit.
基金Ausana Mapook was financially supported by Research and Researchers for Industry Program(RRI)PHD57I0012,Thailand and the German Academic Exchange Service(DAAD)for a joint TRF-DAAD(PPP 2017–2018)academic exchange grant to Kevin D.Hyde and Marc Stadler.Kevin D.Hyde thanks to the 2019 high-end foreign expert introduction plan to Kunming Institute of Botany(granted by the Ministry of Science and Technology of the People’s Republic of China,Grant Number G20190139006)Thailand Research grants entitled Biodiversity,phylogeny and role of fungal endophytes on above parts of Rhizophora apiculata and Nypa fruticans(Grant No:RSA5980068)+1 种基金the future of specialist fungi in a changing climate:baseline data for generalist and specialist fungi associated with ants,Rhododendron species and Dracaena species(Grant No:DBG6080013)Impact of climate change on fungal diversity and biogeography in the Greater Mekong Subregion(Grant No:RDG6130001).
文摘This article provides morphological descriptions and illustrations of microfungi associated with the invasive weed,Chro-molaena odorata,which were mainly collected in northern Thailand.Seventy-seven taxa distributed in ten orders,23 families(of which Neomassarinaceae is new),12 new genera(Chromolaenicola,Chromolaenomyces,Longiappendispora,Pseudocapulatispora,Murichromolaenicola,Neoophiobolus,Paraleptospora,Pseudoroussoella,Pseudostaurosphaeria,Pseudothyridariella,Setoarthopyrenia,Xenoroussoella),47 new species(Aplosporella chromolaenae,Arthrinium chromolae-nae,Chromolaenicola chiangraiensis,C.lampangensis,C.nanensis,C.thailandensis,Chromolaenomyces appendiculatus,Diaporthe chromolaenae,Didymella chromolaenae,Dyfrolomyces chromolaenae,Leptospora chromolaenae,L.phraeana,Longiappendispora chromolaenae,Memnoniella chromolaenae,Montagnula chiangraiensis,M.chromolaenae,M.chromo-laenicola,M.thailandica,Murichromolaenicola chiangraiensis,M.chromolaenae,Muyocopron chromolaenae,M.chromo-laenicola,Neomassarina chromolaenae,Neoophiobolus chromolaenae,Neopyrenochaeta chiangraiensis,N.chromolaenae,N.thailandica,N.triseptatispora,Nigrograna chromolaenae,Nothophoma chromolaenae,Paraleptospora chromolaenae,P.chromolaenicola,Patellaria chromolaenae,Pseudocapulatispora longiappendiculata,Pseudoroussoella chromolaenae,Pseudostaurosphaeria chromolaenae,P.chromolaenicola,Pseudothyridariella chromolaenae,Pyrenochaetopsis chromolae-nae,Rhytidhysteron chromolaenae,Setoarthopyrenia chromolaenae,Sphaeropsis chromolaenicola,Tremateia chiangraiensis,T.chromolaenae,T.thailandensis,Xenoroussoella triseptata,Yunnanensis chromolaenae),12 new host records,three new taxonomic combinations(Chromolaenicola siamensis,Pseudoroussoella elaeicola,Pseudothyridariella mahakashae),and two reference specimens(Torula chromolaenae,T.fici)are described and illustrated.Unlike some other hosts,e.g.bamboo(Poaceae)and Pandanaceae,the dominant group of fungi on Siam weed were Dothideomycetes.Only 15 species previously recorded from northern Thailand were found in this study.Most of the taxa are likely to have jumped hosts from surrounding plants and are unlikely to be a specialist to Siam weed.Most fungal families found on Siam weed had divergence estimates with stem ages in the Cretaceous,which coincided with the expected origin of the host family(Asteraceae).This further indicates that the species have jumped hosts,as it is unlikely that the taxa on the alien Siam weed came from the Americas with its host.They may,however,have jumped from other Asteraceae hosts.In a preliminary screening 40(65%)of the 62 species tested showed antimicrobial activity and thus,the fungi associated with C.odorata may be promising sources of novel bioactive compound discovery.We provide a checklist of fungi associated with C.odorata based on the USDA Systematic Mycology and Microbiology Laboratory(SMML)database,relevant literature and our study.In total,130 taxa(116 identified and 14 unidentified species)are distributed in 20 orders,48 families and 85 genera.Pseudocercospora is the most commonly encountered genus on Siam weed.
基金s The authors appreciate the financial support and postgraduate scholarship provided by State Key Laboratory of Mycology,Institute of Microbiology,Chinese Academy of Sciences,Beijing,China and Mushroom Research Foundation,Chiang Mai,Thailand.National Research Council of Thailand(Mae Fah Luang University)for a grants“Biodiversity,phylogeny and role of fungal endophytes of Pandanaceae”(Grant No.:592010200112)Thailand Research Fund(TRF)entitled“Biodiversity,phylogeny and role of fungal endophytes on above parts of Rhizophora apiculata and Nypa fruticans”(Grant no RSA5980068)National Research Council of Thailand(Mae Fah Luang University)entitled“Diseases of mangrove trees and maintenance of good forestry practice”(Grant no 60201000201)are thanked for the financial support.Authors extend their grateful acknowledgment to PDD,S,B,BISH,IMI,K,IFRD,PH,BRIP,E,MEXU,NY,UPS,TROM and all other herbaria for kindly loaning the herbarium material for the study.C.Suraweera,N.P Daranagama,V.K.Daranagama,and Ruvishika Jayewardene are also thanked for the support provided during the preparation of this manuscript.Lucy Wendt is thanked for the critical reading of part of this manuscript and Jaques Fournier is thanked for the specimens.
文摘Species and generic recognition in the order Xylariales has been uncertain due to lack of molecular data from authentic cultures,as well as overlapping morphological characteristics.In this study,we revise the families Graphostromataceae,Hypoxylaceae,Lopadostomataceae and Xylariaceae in Xylariales.Our study is based on DNA sequence data derived from living cultures of fresh isolates,data from GenBank and morphological observation of type and worldwide herbarium specimens.We also collected new specimens from Germany,Italy and Thailand.Combined analyses of ITS,LSU,RPB2 and b-tubulin sequence data were used to reconstruct the molecular phylogeny of the above families.Generic and familiar boundaries between these families are revised and presented in an updated combined phylogenetic tree.We accept six genera in Graphostromataceae,19 genera in Hypoxylaceae,four in Lopadostomataceae and 37 genera in Xylariaceae.Five genera previously treated in Xylariaceae are placed in Amphisphaeriales genera incertae sedis and seven genera are placed in Xylariales genera incertae sedis.Two genera are placed in Sordariomycetes genera incertae sedis,while four genera are placed as Xylariomycetidae genera incertae sedis.Three genera are considered as doubtful.Barrmaelia and Cannonia,presently included in Xylariaceae are transferred to Diatrypaceae and Coniochaetales respectively,based on their morphology and phylogeny.Areolospora and Myconeesia are excluded from Xylariaceae and synonymized with Phaeosporis and Anthostomella respectively.Updated descriptions and illustrations are provided for all taxa with notes provided on each genus.Excluded and doubtful genera are listed with notes on their taxonomy and phylogeny.Taxonomic keys are provided for all revised families with morphological details for genera within the families.
基金Estonian Science Foundation grants PSG136,PRG632,PUT1170the University of Tartu(PLTOM20903)the European Regional Development Fund(Centre of Excellence EcolChange).
文摘The cryptic lifestyle of most fungi necessitates molecular identification of the guild in environmental studies.Over the past decades,rapid development and affordability of molecular tools have tremendously improved insights of the fungal diversity in all ecosystems and habitats.Yet,in spite of the progress of molecular methods,knowledge about functional properties of the fungal taxa is vague and interpretation of environmental studies in an ecologically meaningful manner remains challenging.In order to facilitate functional assignments and ecological interpretation of environmental studies we introduce a user friendly traits and character database FungalTraits operating at genus and species hypothesis levels.Combining the information from previous efforts such as FUNGuild and FunFun together with involvement of expert knowledge,we reannotated 10,210 and 151 fungal and Stramenopila genera,respectively.This resulted in a stand-alone spreadsheet dataset covering 17 lifestyle related traits of fungal and Stramenopila genera,designed for rapid functional assignments of environmental stud-ies.In order to assign the trait states to fungal species hypotheses,the scientific community of experts manually categorised and assigned available trait information to 697,413 fungal ITS sequences.On the basis of those sequences we were able to summarise trait and host information into 92,623 fungal species hypotheses at 1%dissimilarity threshold.
基金Kevin D.Hyde would like to thank the Thailand Research Fund for a grant entitled“Impact of climate change on fungal diversity and biogeography in the Greater Mekong Sub region(grant no:RDG6130001)for supporting this study.Jian-Kui(Jack)Liu thanks the Joint Fund of the National Natural Science Foundation of China and the Karst Science Research Center of Guizhou province(Grant No.U1812401)This research work was supported by Chiang Mai University.Milan C.Samarakoon is grateful to the Mushroom Research Foundation(MRF),Chiang Rai,Thailand for providing a Postgraduate Scholarship.Mark Brönstrup thanks for support from EMBRIC,the EU-funded European Marine Biological Research Infrastructure Cluster[654008].
文摘Molecular phylogenetic studies of cultures derived from some specimens of plant-inhabiting Sordariomycetes using ITS,LSU,rpb2 and tub2 DNA sequence data revealed close affinities to strains of Muscodor.The taxonomy of this biotechnologi-cally important genus,which exclusively consists of endophytes with sterile mycelia that produce antibiotic volatile secondary metabolites,was based on a rather tentative taxonomic concept.Even though it was accommodated in Xylariaceae,its phylo-genetic position had so far remained obscure.Our phylogeny shows that Muscodor species have affinities to the xylarialean genera Emarcea and Induratia,which is corroborated by the fact that their sexual states produce characteristic apiospores.These data allow for the integration of Muscodor in Induratia,i.e.the genus that was historically described first.The multi-locus phylogenetic tree clearly revealed that a clade comprising Emarcea and Induratia forms a monophylum separate from representatives of Xylariaceae,for which we propose the new family Induratiaceae.Divergence time estimations revealed that Induratiaceae has been diverged from the Xylariaceae+Clypeosphaeriaceae clade at 93(69-119)million years ago(Mya)with the crown age of 61(39-85)Mya during the Cretaceous period.The ascospore-derived cultures were studied for the production of volatile metabolites,using both,dual cultures for assessment of antimicrobial effects and extensive analyses using gas chromatography coupled with mass spectrometry(GC-MS).The antimicrobial effects observed were significant,but not as strong as in the case of the previous reports on Muscodor species.The GC-MS results give rise to some doubt on the validity of the previous identification of certain volatiles.Many peaks in the GC-MS chromatograms could not be safely identified by database searches and may represent new natural products.The isolation of these compounds by preparative chromatography and their subsequent characterisation by nuclear magnetic resonance(NMR)spectroscopy or total synthesis will allow for a more concise identification of these volatiles,and they should also be checked for their individual contri-bution to the observed antibiotic effects.This will be an important prerequisite for the development of biocontrol strains.
基金National Natural Science Foundation of China for supporting the project Biodiversity,Taxonomy,Phylogeny,Evolution and Phytogeography of phytopathogens in Dothideomycetes from Southern China(Grant No.31950410548)for funding this research.Ning Xie would like to thank Project of DEGP(2019KTSCX150)+29 种基金.Kevin D Hyde thanks the Thailand Research Fund for the grant RDG6130001 entitled“Impact of climate change on fungal diversity and biogeography in the Greater Mekong Subregion”.Rungtiwa Phookamsak thanks CAS President’s International Fellowship Initiative(PIFI)for young staff(Grant No.Y9215811Q1)the Yunnan Provincial Department of Human Resources and Social Security(Grant No.Y836181261)National Science Foundation of China(NSFC)project code 31850410489(Grant No.Y81I982211)for financial supportDhanushka Wanasinghe would like to thank CAS President’s International Fellowship Initiative(PIFI)for funding his postdoctoral research(number 2019PC0008)the 64th batch of China Postdoctoral Science Foundation(Grant No.Y913083271).Vemuri V.Sarma would like to thank SERB,Department of Science and Technology,Government of India,for funding a project(SERB/SB/SO/PS/18/2014 dt.19.5.2015)Ministry of Earth Sciences(MOES),Govt.of India for funding a project(Sanction order:MOES/36/OO1S/Extra/40/2014/PC-IV dt.14.01.2015)the Department of Biotechnology,Pondicherry University for facilitiesthe National Research Council of Thailand(projects no.61215320013 and No.61215320023)the Thailand Research Fund(project no.TRG6180001)Plant Genetic Conservation Project under the Royal Initiation of Her Royal High-ness Princess Maha Chakri Sirindhorn-Mae Fah Luang University.Alan JL Phillips acknowledges the support from UIDB/04046/2020 and UIDP/04046/2020 Centre grants from FCT,Portugal(to Bio-ISI).Saowaluck Tibpromma would like to thank the International Postdoctoral Exchange Fellowship Program(number Y9180822S1)CAS President’s International Fellowship Initiative(PIFI)(number 2020PC0009)the National Natural Science Foundation of China(Project Nos.31800010 and 31750001)for financial support.the National Natural Science Foundation of China(No.NSFC 31950410558)Guizhou Medical University(grant number FAMP201906K)tthe National Nat-ural Science Foundation of China(No.NSFC 31760013)the Scientific Research Foundation of Yunnan Provincial Department of Education(2017ZZX186)the Thousand Talents Plan,Youth Project of Yun-nan Provinces for finance supportthe 5th batch of Postdoctoral Orientation Training Personnel in Yunnan Province(Grant No.Y934283261)the 64th batch of China Postdoctoral Science Foundation(Grant No.Y913082271)M Niranjan thanks SERB,Govt.of India for a fellow-ship.Huang Zhang would like to thank Natural Science Foundation of China(NSF 31500017).Jadson DP Bezerra thanks the Conselho Nacional de Desenvolvimento Científico e Tecnológico(CNPq),the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior(CAPES,Finance Code 001)the Fundação de AmparoàCiência e Tecnologia de Pernambuco(FACEPE)for fellowship.B.Devadatha thanks MOES,Govt.of India for a fellowship.Hai-Xia Wu would like to the Fundamental Research Funds for the Central Non-profit Research Institution of CAF(Grant No.CAFYBB2019QB005)the Ten Thousand Talents Plan,Youth Top Project of Yunnan Provinces for finance support.Ausana Mapook thanks to Research and Research-ers for Industries(RRI)under Thailand Research Fund for a personal grant(PHD57I0012)Putarak Chomnunti would like to thank Mae Fah Luang University(Grant No.DR256201012003)Diversity-Based Economy Development Office and National Research Council of Thailand Research(Grant No.T2561022)for the financial support.Satinee Suetrong thanks the collaborative project between BIOTEC and Department of Marine and Coastal Resources(DMCR),Ministry of Natural Resources and Environmentunder a project:Marine Microbes for National Reserves:Alternative Ways of State Property.N.Chai-wan would like to thank the Thailand Research Fund(PHD60K0147).
文摘Numerous new taxa and classifications of Dothideomycetes have been published following the last monograph of families of Dothideomycetes in 2013.A recent publication by Honsanan et al.in 2020 expanded information of families in Dothideo-mycetidae and Pleosporomycetidae with modern classifications.In this paper,we provide a refined updated document on orders and families incertae sedis of Dothideomycetes.Each family is provided with an updated description,notes,including figures to represent the morphology,a list of accepted genera,and economic and ecological significances.We also provide phylogenetic trees for each order.In this study,31 orders which consist 50 families are assigned as orders incertae sedis in Dothideomycetes,and 41 families are treated as families incertae sedis due to lack of molecular or morphological evidence.The new order,Catinellales,and four new families,Catinellaceae,Morenoinaceae Neobuelliellaceae and Thyrinulaceae are introduced.Seven genera(Neobuelliella,Pseudomicrothyrium,Flagellostrigula,Swinscowia,Macroconstrictolumina,Pseudobogoriella,and Schummia)are introduced.Seven new species(Acrospermum urticae,Bogoriella complexoluminata,Dothiorella ostryae,Dyfrolomyces distoseptatus,Macroconstrictolumina megalateralis,Patellaria microspora,and Pseu-domicrothyrium thailandicum)are introduced base on morphology and phylogeny,together with two new records/reports and five new collections from different families.Ninety new combinations are also provided in this paper.
文摘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 appres-soria 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.
基金Saowaluck Tibpromma would like to thank the Molecular Biology Experimental Center at Kunming Institute of Botany for facilities for molecular work,the Mushroom Research Foundation(MRF)Chiang Rai,Thailand for the financial support of her study and Shaun Pennycook is thanked for nomenclatural advice.K.D.Hyde would like to thank the Thailand Research Fund Grant No.RSA5980068 entitled“Biodiversity,phylogeny and role of fungal endophytes on above parts of Rhizophora apiculata and Nypa fruticans”+21 种基金the Chinese Academy of Sciences,Project Number 2013T2S0030for the award of Visiting Professorship for Senior International Scientists at Kunming Institute of Botany and National Research Council of Thailand(Mae Fah Luang University)for a grants“Biodiversity,phylogeny and role of fungal endophytes of Pandanaceae”(Grant No.:592010200112)“Diseases of mangrove trees and maintenance of good forestry practice”(Grant No.:60201000201)for supporting this study.S.C.Karunarathna,P.E.Mortimer and J.C.Xu would like to thank the World Agroforestry Centre,East and Central Asia OfficeKey Laboratory for Plant Diversity and Biogeography of East Asia,Kunming Institute of Botany,Chinese Academy of Sciencethe ChineseMinistry of Science and Technology,under the 12th 5-year National Key Technology Support Program(NKTSP)2013 BAB07B06 integration and comprehensive demonstration of key technologies on Green Phosphate-mountaion Construction and the CGIAR Research Program 6:Forest,Trees and Agroforestry for partial funding.The authors would like to extend their sincere appreciation to the Deanship of Scientific Research at King Saud University for funding this research group NO(RG-1436-025)Financial support by the German Academic Exchange Service(DAAD)and the Thai Royal Golden Ph.D.Jubilee-Industry program(RGJ)for a joint TRFDAAD PPP(2012-2014)academic exchange grant to K.D.Hyde and M.Stadler,and the RGJ for a personal grant to B.Thongbai(No.Ph.D/0138/2553 in 4.S.MF/53/A.3)is gratefully acknowledged.Chayanard Phukhamsakda(PHD/0020/2557)acknowledges the Royal Golden Jubilee Ph.D.Program under the Thailand Research Fund.Mingkwan Doilom acknowledges the Royal Golden Jubilee Ph.D.Program(PHD./0072/2553 in 4.S.M.F./53/A.2)under the Thailand Research Fund.Ausana Mapook is grateful to Research and Researchers for Industries(RRI)PHD57I0012.Rungtiwa Phookamsak expresses sincere appreciation to The CAS President’s International Fellowship for Postdoctoral Researchers(Project No.2017PB0072)Qi Zhao thanks the National Natural Science Foundation of China(No.31360015)the CAS/SAFEA International Partnership Program for Creative Research Teams,and the Knowledge Innovation Program of the Chinese Academy of Sciences(No.KSCX2-EW-Z-9 and KIB2016002).Andre´Luiz Cabral Monteiro de Azevedo Santiago,Carlos Alberto Fragoso de Souza,Diogo Xavier Lima,Rafael Jose´Vilela de Oliveira and Gladstone Alves da Silva would like to thank the Coordenac¸a˜o de Aperfeic¸oamento de Pessoal de Nı´vel Superior(Coordination for the Improvement of Higher Education Personnel)(CAPES)and the Fundac¸a˜o de Amparo a`Cieˆncia e Tecnologia do Estado de Pernambuco(Foundation for the support of Science and Technology of the state of Pernambuco)(FACEPE)for the postgraduate scholarships awarded to Diogo X.Lima and Carlos A.F.de Souza,respectively.We would also like to thank the Conselho Nacional de Desenvolvimento Cientı´fico e Tecnolo´gico(National Council for Scientific and Technological Development)(CNPq)and FACEPE for financial support through the projects:‘Mucoromycotina in upland forests in the semi-arid region of Pernambuco’(CNPq-458391/2014-0)‘Diversity of Mucoromycotina in different ecosystems of the Pernambuco Atlantic Rainforest’(FACEPE-APQ 0842-2.12/14).H.B.Lee was supported by the Graduate Program for the Undiscovered Taxa of Korea,and by the Project on Survey and Discovery of Indigenous Fungal Species of Korea funded by NIBR and Project on Discovery of Fungi from Freshwater and Collection of Fungarium funded by NNIBR of the Ministry of Environment(MOE)and in part by a fund from National Institute of Animal Science under Rural Development Administration,Republic of Korea.Z.L Luo and H.Y Su would like to thank the National Natural Science Foundation of China(Project ID:31460015)for financial support on Study of the distribution pattern and driving factors of aquatic fungal diversity in the region of Three Parallel Rivers.Saranyaphat Boonmee thanks the National Research Council of Thailand,project number 2560A30702021the Thailand Research Fund,project number TRG5880152 for providing financial support.C.G.Lin and Y.Wang thank the grant from the National Natural Science Foundation of China(No.NSFC 31560489)Fundamental Research on Science and Technology,Ministry of Science and Technology of China(2014FY120100)Mr.Jingzu Sun thank for the National Natural Science Foundations of China(No.31600024)Wei Dong thanks the for National Natural Science Foundation of China(Project ID:NSF 31500017 to Huang Zhang)P.N.Singh,A.Baghela,S.K.Singh,and S.Aamir thank the Director,MACS’Agharkar Research Institute,Pune,India for providing facilities and Rajendra Singh(Department of Zoology,DDU Gorakhpur University,UP,India)for identification of insect-host.Saisamorn Lumyong and Rene K.Schumacher are thanked for valuable suggestions and collecting specimens.K.N.A.Raj acknowledges support from the University Grants Commission(UGC)India,in the form of a Rajiv Gandhi National Fellowship(Grant No.F.14-2(SC)/2009(SA-III))K.N.A.Raj also acknowledges the permissions given to him for collecting agaric specimens from the forests of Kerala by the Principal Chief Conservator of Forests,Government of Kerala(WL12-4042/2009 dated 5 August 2009).K.P.D.Latha acknowledges the financial support from the Kerala State Council for Science,Technology and Environment(KSCSTE)in the form of a PhD fellowship(Grant No.001/FSHP/2011/CSTE)K.P.D.Latha also acknowledges the permission(No.WL10-4937/2012,dated 3-10-2013)given to her by the Principal Chief Conservator of Forests,Government of Kerala,to collect agaric specimens from the forests of Kerala.Zdenko Tkalcec has been partially supported by Croatian Science Foundation under the project HRZZ-IP-11-2013-2202(ACCTA)is grateful to Milan Cerkez for his great contribution to the study of coprinoid and coprophilous fungi in Croatia.Vladimir Antonı´n thank the Moravian Museum by the Ministry of Culture of the Czech Republic as part of its long-term conceptual development programme for research institutions(DKRVO,ref.MK000094862)T.C.Wen,Y.P.Xiao,C.Norphanphoun and K.K.Hapuarachchi are grateful to the National Natural Science Foundation of China(No.31460012)and the Science and Technology Foundation of Guizhou Province(No.[2016]2863)Y.W.Lim would like to thanks NIBR supporting the Project on Survey and Discovery of Indigenous Fungal Species of Korea.Kanad Das and Dyutiparna Chakraborty are thankful to the Director,Botanical Survey of India(BSI)and Scientist-in-Charge,BSI,Gangtok for providing facilities during this study.Sinchan Adhikari,Joydeep Karmakar and Tapas Kumar Bandyopadhyay would like to acknowledge DST-PURSE and DST-FIST for providing central instrumentation facilities and Alan JL Phillips acknowledges the Biosystems and Integrative Sciences Institute(BioISI,FCT/UID/Multi/04046/2013).
文摘This is a continuity of a series of taxonomic and phylogenetic papers on the fungi where materials were collected from many countries,examined and described.In addition to extensive morphological descriptions and appropriate asexual and sexual connections,DNA sequence data are also analysed from concatenated datasets to infer phylogenetic relationships and substantiate systematic positions of taxa within appropriate ranks.Wherever new species or combinations are proposed,we apply an integrative approach using morphological and molecular data as well as ecological features wherever applicable.Notes on 112 fungal taxa are compiled in this paper including Biatriosporaceae and Roussoellaceae,Didysimulans gen.nov.,81 new species,18 new host records and new country records,five reference specimens,two new combinations,and three sexual and asexual morph reports.The new species are Amanita cornelii,A.emodotrygon,Angustimassarina alni,A.arezzoensis,A.italica,A.lonicerae,A.premilcurensis,Ascochyta italica,A.rosae,Austroboletus appendiculatus,Barriopsis thailandica,Berkleasmium ariense,Calophoma petasitis,Camarosporium laburnicola,C.moricola,C.grisea,C.ossea,C.paraincrustata,Colletotrichum sambucicola,Coprinopsis cerkezii,Cytospora gelida,Dacrymyces chiangraiensis,Didysimulans italica,D.mezzanensis,Entodesmium italica,Entoloma magnum,Evlachovaea indica,Exophiala italica,Favolus gracilisporus,Femsjonia monospora,Fomitopsis flabellata,F.roseoalba,Gongronella brasiliensis,Helvella crispoides,Hermatomyces chiangmaiensis,H.chromolaenae,Hysterium centramurum,Inflatispora caryotae,Inocybe brunneosquamulosa,I.luteobrunnea,I.rubrobrunnea,Keissleriella cirsii,Lepiota cylindrocystidia,L.flavocarpa,L.maerimensis,Lophiotrema guttulata,Marasmius luculentus,Morenoina calamicola,Moelleriella thanathonensis,Mucor stercorarius,Myrmecridium fluviae,Myrothecium septentrionale,Neosetophoma garethjonesii,Nigrograna cangshanensis,Nodulosphaeria guttulatum,N.multiseptata,N.sambuci,Panus subfasciatus,Paraleptosphaeria padi,Paraphaeosphaeria viciae,Parathyridaria robiniae,Penicillium punicae,Phaeosphaeria calamicola,Phaeosphaeriopsis yuccae,Pleurophoma italica,Polyporus brevibasidiosus,P.koreanus,P.orientivarius,P.parvovarius,P.subdictyopus,P.ulleungus,Pseudoasteromassaria spadicea,Rosellinia mearnsii,Rubroboletus demonensis,Russula yanheensis,Sigarispora muriformis,Sillia italica,Stagonosporopsis ailanthicola,Strobilomyces longistipitatus,Subplenodomus galicola and Wolfiporia pseudococos.The new combinations are Melanomma populina and Rubroboletus eastwoodiae.The reference specimens are Cookeina tricholoma,Gnomoniopsis sanguisorbae,Helvella costifera,Polythrincium trifolii and Russula virescens.The new host records and country records are Ascochyta medicaginicola,Boletellus emodensis,Cyptotrama asprata,Cytospora ceratosperma,Favolaschia auriscalpium,F.manipularis,Hysterobrevium mori,Lentinus sajor-caju,L.squarrosulus,L.velutinus,Leucocoprinus cretaceus,Lophiotrema vagabundum,Nothophoma quercina,Platystomum rosae,Pseudodidymosphaeria phlei,Tremella fuciformis,Truncatella spartii and Vaginatispora appendiculata and three sexual and asexual morphs are Aposphaeria corallinolutea, Dothiorabuxi and Hypocrella calendulina.
文摘This paper provides illustrated descriptions of micro-fungi newly found on Pandanaceae in China and Thailand.The fungi are accommodated in 31 families.New taxa described include a new family,seven new genera,65 new species,16 previously known species.A new family:Malaysiascaceae(Glomerellales).New genera are Acremoniisimulans(Plec-tosphaerellaceae),Pandanaceomyces,Pseudoachroiostachy(Nectriaceae),Pseudohyaloseta(Niessliaceae),Pseudoor-natispora(Stachybotriaceae)and Yunnanomyces(Sympoventuriaceae).New species are Acremoniisimulans thailandensis,Beltrania krabiensis,Beltraniella pandanicola,B.thailandicus,Canalisporium krabiense,C.thailandensis,Clonostachys krabiensis,Curvularia chonburiensis,C.pandanicola,C.thailandicum,C.xishuangbannaensis,Cylindrocladiella xishuangbannaensis,Dictyochaeta pandanicola,Dictyocheirospora nabanheensis,D.pandanicola,D.xishuangbannaen-sis,Dictyosporium appendiculatum,Di.guttulatum,Di.hongkongensis,Di.krabiense,Di.pandanicola,Distoseptispora thailandica,D.xishuangbannaensis,Helicoma freycinetiae,Hermatomyces biconisporus,Lasiodiplodia chonburiensis,L.pandanicola,Lasionectria krabiense,Menisporopsis pandanicola,Montagnula krabiensis,Musicillium pandanicola,Neofusicoccum pandanicola,Neohelicomyces pandanicola,Neooccultibambusa thailandensis,Neopestalotiopsis chiang-maiensis,N.pandanicola,N.phangngaensis,Pandanaceomyces krabiensis,Paracylindrocarpon nabanheensis,P.pan-danicola,P.xishuangbannaensis,Parasarcopodium hongkongensis,Pestalotiopsis krabiensis,P.pandanicola,Polyplosphaeria nabanheensis,P.pandanicola,P.xishuangbannaensis,Pseudoachroiostachys krabiense,Pseu-doberkleasmium pandanicola,Pseudochaetosphaeronema pandanicola,Pseudohyaloseta pandanicola,Pseudoornatispora krabiense,Pseudopithomyces pandanicola,Rostriconidium pandanicola,Sirastachys phangngaensis,Stictis pandanicola,Terriera pandanicola,Thozetella pandanicola,Tubeufia freycinetiae,T.parvispora,T.pandanicola,Vermiculariopsiella hongkongensis,Volutella krabiense,V.thailandensis and Yunnanomyces pandanicola.Previous studies of micro-fungi on Pandanaceae have not included phylogenetic support.Inspiration for this study came from the book Fungi Associated with Pandanaceae by Whitton,McKenzie and Hyde in 2012.Both studies reveal that the micro-fungi on Pandanaceae is particularly rich in hyphomycetes.All data presented herein are based on morphological examination of specimens,coupled with phylogenetic sequence data to better integrate taxa into appropriate taxonomic ranks and infer their evolu-tionary relationships.
基金Danny Haelewaters is supported by the Research Foundation-Flanders(junior postdoctoral fellowship 1206620N)Dhanushka Wanasinghe thanks the CAS President’s International Fellowship Initiative(PIFI)for funding his postdoctoral research(number 2021FYB0005)the Postdoctoral Fund from Human Resources and Social Security Bureau of Yunnan Province.
文摘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 fore-most 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 differ-ent 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.
基金Acknowledgements Nalin Wijayawardene would like to thank Lechat Christian,Yuanpin Xiao,Danushka Sandaruwan,Paul Mungai,Huang Zhang,Ishani Goonasekara,Chada Norphanphoun,Ishara Manawasingha,Rajesh Jeewon,Thilini Chethana and Hasini Ekanayaka for their assistances and suggestions.We would like to thank Mark Stadler for his help to check names in Xylariales.Nalin Wijayawardene and Pedro Crous thank Ulrike Damm for her comments and suggestions for validating several names.K.D.Hyde thanks The Chinese Academy of Sciences,for the award of Visiting Professorship for Senior International Scientists at Kunming Institute of Botany.K.D.Hyde and Monika C.Dayarathne would like to thank the Thailand Research Fund(TRF)grant no RSA5980068 entitled Biodiversity,phylogeny and role of fungal endophytes on above parts of Rhizophora apiculata and Nypa fruticans,National Research Council of Thailand(NRCT)entitled Diseases of mangrove trees and maintenance of good forestry practice(Grant number:60201000201)Mae Fah Luang University grant"Biodiversity,phylogeny and role of fungal endophytes of Pandanaceae"(Grant number:592010200112)+9 种基金Hugo Madrid was funded by Comisio´n Nacional de Investigacio´n Cientı´fica y Tecnolo´gica(CONICYT)Fondo Nacional de Desarrollo Cientı´fico y Tecnolo´gico(FONDECYT),Chile,project no.11140562."Rafael F.Castan˜eda-Ruiz is grateful to the Organizacio´n Superior de Direccio´n Empresarial,Grupo Agrı´cola,(OSDE)from the Cuban Ministry of Agriculture and"Programa de Salud Animal y Vegetal",project P131LH003033.Dong Qin Dai would like to thank the Key Laboratory of Yunnan Province Universities of the Diversity and Ecological Adaptive Evolution for Animals and plants on Yun-Gui Plateau for the support.Ka-Lai Pang thanks Ministry of Science and Technology,Taiwan for financial support(105-2621-B-019-002-)Guo Zhu Zhao was funded by the National Natural Science Foundation of China(No.31570019)Mingkwan Doilom acknowledges the Royal Golden Jubilee Ph.D.Program(PHD./0072/2553 in 4.S.M.F./53/A.2.K.Tanaka would like to thank the Japan Society for the Promotion of Science(JSPS26291084 and 16K07474)Walter P.Pfliegler was supported through the U´NKP-16-4-IV New National Excellence Program of the Hungarian Ministry of Human Capacities.Samantha C.Karunarathna thanks Yunnan Provincial Department of Human Resources and Social Security funded postdoctoral project(number 179122)for supporting his postdoctoral research study.The authors extend their appreciation to the International Scientific Partnership Program ISPP at King Saud University for funding this research work through ISPP#0089.KC Rajeshkumar thanks SERB,DST,Government of India for providing financial support under the project YSS/2015/001590Dr.K.M.Paknikar,Director,ARI for providing the facility.Mats Wedin thanks the Swedish Research Council,grants VR 621-2012-3990VR 2016-03589.Alan JL Phillips acknowledges the support from Biosystems and Integrative Sciences Institute(BioISI,FCT/UID/Multi/04046/2013)L.Selbmann,L.Zucconi and S.Onofri thank the Italian National Program for Antarctic Researches(PNRA)for the financial support.The Italian National Antarctic Museum(MNA)is acknowledged for supporting the Mycological Section and the Culture Collection of Fungi from Extreme Environments(CCFEE).
文摘Knowledge of the relationships and thus the classification of fungi,has developed rapidly with increasingly widespread use of molecular techniques,over the past 10–15 years,and continues to accelerate.Several genera have been found to be polyphyletic,and their generic concepts have subsequently been emended.New names have thus been introduced for species which are phylogenetically distinct from the type species of particular genera.The ending of the separate naming of morphs of the same species in 2011,has also caused changes in fungal generic names.In order to facilitate access to all important changes,it was desirable to compile these in a single document.The present article provides a list of generic names of Ascomycota(approximately 6500 accepted names published to the end of 2016),including those which are lichen-forming.Notes and summaries of the changes since the last edition of‘Ainsworth&Bisby’s Dictionary of the Fungi’in 2008 are provided.The notes include the number of accepted species,classification,type species(with location of the type material),culture availability,life-styles,distribution,and selected publications that have appeared since 2008.This work is intended to provide the foundation for updating the ascomycete component of the"Without prejudice list of generic names of Fungi"published in 2013,which will be developed into a list of protected generic names.This will be subjected to the XIXth International Botanical Congress in Shenzhen in July 2017 agreeing to a modification in the rules relating to protected lists,and scrutiny by procedures determined by the Nomenclature Committee for Fungi(NCF).The previously invalidly published generic names Barriopsis,Collophora(as Collophorina),Cryomyces,Dematiopleospora,Heterospora(as Heterosporicola),Lithophila,Palmomyces(as Palmaria)and Saxomyces are validated,as are two previously invalid family names,Bartaliniaceae and Wiesneriomycetaceae.Four species of Lalaria,which were invalidly published are transferred to Taphrina and validated as new combinations.Catenomycopsis Tibell&Constant.is reduced under Chaenothecopsis Vain.,while Dichomera Cooke is reduced under Botryosphaeria Ces.&De Not.(Art.59).
文摘This article is the 15th contribution in the Fungal Diversity Notes series,wherein 115 taxa from three phyla,nine classes,28 orders,48 families,and 64 genera are treated.Fungal taxa described and illustrated in the present study include a new family,five new genera,61 new species,five new combinations,one synonym,one new variety and 31 records on new hosts or new geographical distributions.Ageratinicolaceae fam.nov.is introduced and accommodated in Pleosporales.The new genera introduced in this study are Ageratinicola,Kevinia,Pseudomultiseptospora(Parabambusicolaceae),Marasmiellomycena,and Vizzinia(Porotheleaceae).Newly described species are Abrothallus altoandinus,Ageratinicola kunmingensis,Allocryptovalsa aceris,Allophoma yuccae,Apiospora cannae,A.elliptica,A.pallidesporae,Boeremia wisteriae,Calycina papaeana,Clypeo-coccum lichenostigmoides,Coniochaeta riskali-shoyakubovii,Cryphonectria kunmingensis,Diaporthe angustiapiculata,D.campylandrae,D.longipapillata,Diatrypella guangdongense,Dothiorella franceschinii,Endocalyx phoenicis,Epicoc-cum terminosporum,Fulvifomes karaiensis,F.pannaensis,Ganoderma ghatensis,Hysterobrevium baoshanense,Inocybe avellaneorosea,I.lucida,Jahnula oblonga,Kevinia lignicola,Kirschsteiniothelia guangdongensis,Laboulbenia caprina,L.clavulata,L.cobiae,L.cosmodisci,L.nilotica,L.omalii,L.robusta,L.similis,L.stigmatophora,Laccaria rubriporus,Lasiodiplodia morindae,Lyophyllum agnijum,Marasmiellomycena pseudoomphaliiformis,Melomastia beihaiensis,Nemania guangdongensis,Nigrograna thailandica,Nigrospora ficuum,Oxydothis chinensis,O.yunnanensis,Petriella thailandica,Phaeoacremonium chinensis,Phialocephala chinensis,Phytophthora debattistii,Polyplosphaeria nigrospora,Pronectria loweniae,Seriascoma acutispora,Setoseptoria bambusae,Stictis anomianthi,Tarzetta tibetensis,Tarzetta urceolata,Tetraploa obpyriformis,Trichoglossum beninense,and Tricoderma pyrrosiae.We provide an emendation for Urnula ailaoshanensis Agaricus duplocingulatoides var.brevisporus introduced as a new variety based on morphology and phylogeny.
文摘Correction to:Fungal Diversity(2020)105:116 https://doi.org/10.1007/s13225-020-00466-2 There were errors in the name of author LászlóG.Nagy and in affiliation no.31 in the original publication.The original article has been corrected.
