Genomics,transcriptomics,and peptidomics of the greater wax moth Galleria mellonella neuropeptides and their expression in response to lead stress

Neuropeptides are crucial in regulation of a rich variety of developmental,physiological,and behavioral functions throughout the life cycle of insects.Using an integrated approach of multiomics,we identified neuropeptide precursors in the greater wax moth Galleria mellonella,which is a harmful pest of honeybee hives with a worldwide distribution.Here,a total of 63 and 67 neuropeptide precursors were predicted and annotated in the G.mellonella genome and transcriptome,in which 40 neuropeptide precursors were confirmed in the G.mellonella peptidome.Interestingly,we identified 12 neuropeptide precursor genes present in G.mellonella but absent in honeybees,which may be potential novel pesticide target sites.Honeybee hives were contaminated with heavy metals such as lead,enabling its bioaccumulation in G.mellonella bodies through the food chain,we performed transcriptome sequencing to analyze the effects of Pb stress on the mRNA expression level of G.mellonella neuropeptide precursors.After treatment by Pb,the expression of neuropeptide F1 was found to be significantly downregulated,implying that this neuropeptide might be associated with responding to the heavy metal stress in G.mellonella.This study comprehensively identified neuropeptide precursors in G.mellonella,and discussed the effects of heavy metals on insect neuropeptides,with the example of G.mellonella.The results are valuable for future elucidation of how neuropeptides regulate physiological functions in G.mellonella and contribute to our understanding of the insect's environmental plasticity and identify potential new biomarkers to assess heavy metal toxicity in insects.

Natarajania thailandica sp.nov.(Stilbosporaceae,Diaporthales)from Thailand

A fungus similar to the monotypic genus Natarajania,isolated from dead wood and collected in Thailand,is reported.Analysis of partial ribosomal LSU and a protein coding gene(RPB2)demonstrated that the new isolate belonged to Stilbosporaceae,Diaporthales and genetically different from N.indica.It is unique in producing synnematous conidiophores,smooth-walled conidiogenous cells and a flared collarette but lacks an elongated collar-canal which is distinct in the type species.Therefore,sequence data and morphological traits are used to introduce the new species,Natarajania thailandica.

Polycephalomycetaceae,a new family of clavicipitoid fungi segregates from Ophiocordycipitaceae

Clavicipitoid fungi comprise three families,namely Clavicipitaceae,Cordycipitaceae,and Ophiocordycipitaceae.They are found worldwide and are specialized pathogens of invertebrate,plant and fungal hosts.Over the last decade,morphology-and phylogeny-based studies on clavicipitoid fungi have increased.The latter have revealed that Polycephalomyces,Perennicordyceps and Pleurocordyceps consistently cluster together.These genera are currently considered as members of Ophiocordycipitaceae.Nonetheless,information with regard to their diversity and ecology remains sparse.To fill this gap,we collected 29 fresh specimens from insect and fungal substrates from tropical and subtropical evergreen forests in Thailand and southwestern China.We performed detailed morphological analyses and constructed photoplates for all isolated fungi.We used extensive taxon sampling and a dataset comprising internal transcribed spacer gene region(ITS),small subunit ribosomal RNA gene region(SSU),large subunit rRNA gene region(LSU),translation elongation factor 1-alpha gene region(TEF-1α),RNA polymerase II largest subunit gene region(RPB1)and RNA polymerase II second largest subunit(RPB2)to infer order-,family and genus-level phylogenetic trees.Based on these biphasic analyses,we segregate Polycephalomyces,Perennicordyceps,and Pleurocordyceps from Ophiocordycipitaceae and introduce the new family Polycephalomycetaceae to accomodate these three genera.The majority of species in this family have a vast range of insect and fungal hosts.The sexual morph of Polycephalomycetaceae has stromatic ascomata,long stipes,thick peridium,and cylindrical secondary spores.The asexual morph is characterized by colonies on the host surface or synnemata with stipes on the host,one or two types of phialides,and cylindrical to fusiform conidia.We expand the number of taxa in the new family by introducing seven new species(Polycephalomyces albiramus,Perennicordyceps lutea,Pleurocordyceps parvicapitata,Pleurocordyceps lanceolatus,Pleurocordyceps nutansis,Pleurocordyceps heilongtanensis,Pleurocordyceps vitellina),nine new hosts,and one new combination(Perennicordyceps elaphomyceticola).The results herein hint at a high level of diversity for Polycephalomycetaceae.Future investigations focusing on obtaining additional collections and specimens from different geographical areas would help to reveal not only the extent of the group’s diversity,but also resolve its deeper phylogenetic placement.

Profile of Bionectriaceae,Calcarisporiaceae,Hypocreaceae,Nectriaceae,Tilachlidiaceae,Ijuhyaceae fam.nov.,Stromatonectriaceae fam.nov.and Xanthonectriaceae fam.nov

This paper provides outlines for Bionectriaceae,Calcarisporiaceae,Hypocreaceae,Nectriaceae,Tilachlidiaceae,Ijuhy-aceae,Stromatonectriaceae and Xanthonectriaceae with taxonomic treatments.We provide up-to-date DNA sequence-based phylogenies including combined gene analysis of ITS,LSU,rpb2,tef1 and tub2 for Hypocreales and accept 17 families.Three new families and 12 new species are introduced with descriptions and illustrations,while 13 new records and one new species combination are provided.Here we mainly detail the taxonomy of Bionectriaceae,Hypocreaceae,Nectriaceae and Tilachlidiaceae,Ijuhyaceae fam.nov.,Stromatonectriaceae fam.nov.and Xanthonectriaceae fam.nov.are introduced in this study based on phenotypic and molecular analyses.For each family we provide a list of accepted genera,the taxo-nomic history,morphological descriptions,taxonomic placement based on DNA sequence data and illustrate the type genus.Representatives of each family are illustrated based on the type herbarium material or fresh specimens where available,or provide relevant references.Notes on ecological and economic importance of the families are also given.

Diatrypella macrospora,a new host and geographical record from Forlì-Cesena,Italy

During a microfungi survey in the Province of Forlì-Cesena,Italy,a diatrypaceous taxon was collected on a dead branch of Quercus cerris(Fagaceae,Fagales).Phylogenetic analyses of combined ITS andβ-tubulin sequence data identified the taxon as Diatrypella macrospora.This represents a new host and geographical record for D.macrospora.This new collection is similar to the holotype,but differs in having shorter perithecial necks and smaller ascospores with marked curvature.In this account,a detailed description,colour photographs and phylogenetic analyses are provided to represent the new record of D.macrospora.

Species concepts of Dothideomycetes:classification,phylogenetic inconsistencies and taxonomic standardization

The species is one of the basic units of biological classification.Both species concepts and recognition are essential topics in taxonomic studies and other biological research.In the first part of this review,we briefly discuss the taxonomic history of the class Dothideomycetes.In the second part of the paper,we review four commonly used species concepts,focusing on morphological,ecological,biological and phylogenetic criteria and their applicability in the taxonomy of Dothideomycetes.The application and utility of the four criteria is discussed with examples in the genera Ascochyta,Cercospora and Neofu-sicoccum.Some problems and challenges of studying Dothideomycetes are analyzed and basic guidelines for classifying species under the above criteria are provided.

Evolution of freshwater Diaporthomycetidae(Sordariomycetes)provides evidence for five new orders and six new families

Cancellidium is a remarkable fungal genus which has been collected from wood submerged in freshwater and has unique conidia that are important in dispersal in running streams.With such a remarkable morphology,one would have expected it to be a distinct family or order.However,due to the dearth of molecular evidence in related taxa,this genus has previ-ously been placed in the order Hypocreales,subclass Hypocreomycetidae of Sordariomycetes.In this study,we made three new collections of this remarkable aquatic genus from streams in China and Thailand,isolated them into culture,extracted DNA and carried out multigene phylogenetic analysis and divergence time estimation which placed the genus in Diaporthomycetidae.This is one of the seven subclasses of Sordariomycetes and contains 30 lineages that are only known from freshwater.The subclass is therefore of interest when considering the evolution of freshwater fungi.Several lineages of Diaporthomycetidae are morphologically unique and taxa cluster with strong support,but have weak support at the base of the trees.The phylogenetic and MCC trees generated in this study indicate that Aquapteridospora,Barbatosphaeriaceae,Bullimyces,Cancellidium,Ceratolenta,Conlarium,Phialemoniopsis,Pseudostanjehughesia and Rhamphoriaceae are distinct genera/families that evolved in the family/order time frame.The new orders Barbatosphaeriales(177 MYA),Cancellidiales(137 MYA),Ceratolentales(147 MYA),Conlariales(138 MYA)and Rhamphoriales(133 MYA)and six new families,Aquapteridosporaceae(110 MYA),Cancellidiaceae(137 MYA),Ceratolentaceae(81 MYA),Bullimycetaceae(81 MYA),Phialemoniopsaceae(59 MYA),and Pseudostanjehughesiaceae(111 MYA)are introduced with evidence from phylogenies,divergence estimates and distinct morphologies.Of these families,Aquapteridosporaceae,Cancellidiaceae,Bullimycetaceae,and Pseudostanjehughesiaceae are only known from freshwater.

Taxonomic studies of some often over-looked Diaporthomycetidae and Sordariomycetidae

Sordariomycetes is an earlier-introduced and one of the widely distributed class of Ascomycota.The class was initially clas-sified based on morphology in having inoperculate and unitunicate asci.With the development of DNA based phylogenetic analysis,several undetermined or polyphyletic members of Sordariomycetes were reclassified.However,not all species belonging to this class have been sequenced and analyzed.There are a number of species,especially those old and poorly studied ones which have never been sequenced before and not even recollected again for further taxonomic verification.One of the main objective in this study is to revise and update the taxonomy of several well-known early and poorly studied spe-cies whose classification are still obscure.Herein,we re-examined the type materials and/or authentic specimens together to explore 74 relatively poorly-studied genera,which mainly belong to Boliniales,Calosphaeriales,Chaetosphaeriales,Jobellisiales,and Sordariales classified under Diaporthomycetidae and Sordariomycetidae.We provide descriptions,notes,figures and/or drawings and discussed their phylogenetic relationships.As a result,the monotypic Jobellisiales is transferred from Hypocreomycetidae to Diaporthomycetidae.Based on phylogenetic analysis,the polyphyletic Lasiosphaeriaceae is divided into five families,Bombardiaceae(Apodospora,Bombardia,Bombardioidea,Fimetariella and Ramophialophora),Lasiosphaeriaceae(Anopodium,Bellojisia,Corylomyces,Lasiosphaeria,Mammaria and Zopfiella),Lasiosphaeridaceae(Lasiosphaeris),Strattoniaceae(Strattonia)and Zygospermellaceae(Episternus and Zygospermella).In addition,a new family Neoschizotheciaceae is established based on Neoschizothecium.Analysis of the type species of Boothiella,Stel-latospora,Sulcatistroma and Tengiomyces placed them in Sordariaceae,Chaetomiaceae,Hypocreales and Coronophorales,respectively.We classify the genera lacking molecular data based on their morphology and expect them to be recollected;that is,Kacosphaeria in Calosphaeriales;Arnium,Biconiosporella,Camptosphaeria,Diffractella,Emblemospora,Eosphaeria,Periamphispora,Synaptospora and Tripterosporella in Sordariales;Conidiotheca in Sordariomycetes;Copromyces,Effetia,Endophragmiella and Tulipispora are accommodated in Ascomycota.Besides,we establish a new genus Neoschizothecium based on phylogenetic analysis.New combinations proposed:Camaropella amorpha,Cam.microspora,Cam.plana,Clad-orrhinum grandiusculum,Cla.leucotrichum,Cla.terricola,Cla.olerum,Helminthosphaeria plumbea,Immersiella hirta,Jugulospora minor,Lasiosphaeris arenicola,Neoschizothecium aloides,Neo.carpinicola,Neo.conicum,Neo.curvisporum,Neo.fimbriatum,Neo.glutinans,Neo.inaequale,Neo.minicaudum,Neo.selenosporum,Neo.tetrasporum,Neurospora autosteira,Podospora brunnescens,P.flexuosa,P.jamaicensis,P.hamata,P.macrospora,P.spinosa,Strattonia petrogale and Triangularia microsclerotigena,T.nannopodalis,T.praecox,T.samala,T.tarvisina,T.unicaudata,T.yaeyamensis.New epithets are proposed for Apiorhynchostoma apiosporum and Podospora dacryoidea.

The numbers of fungi: is the descriptive curve flattening?

The recent realistic estimate of fungal numbers which used various algorithms was between 2.2 and 3.8 million.There are nearly 100,000 accepted species of Fungi and fungus-like taxa,which is between 2.6 and 4.5%of the estimated species.Several forums such as Botanica Marina series,Fungal Diversity notes,Fungal Biodiversity Profiles,Fungal Systematics and Evolution-New and Interesting Fungi,Mycosphere notes and Fungal Planet have enhanced the introduction of new taxa and nearly 2000 species have been introduced in these publications in the last decade.The need to define a fungal species more accurately has been recognized,but there is much research needed before this can be better clarified.We address the evidence that is needed to estimate the numbers of fungi and address the various advances that have been made towards its understanding.Some genera are barely known,whereas some plant pathogens comprise numerous species complexes and numbers are steadily increasing.In this paper,we examine ten genera as case studies to establish trends in fungal description and introduce new species in each genus.The genera are the ascomycetes Colletotrichum and Pestalotiopsis(with many species or complexes),Atrocalyx,Dothiora,Lignosphaeria,Okeanomyces,Rhamphoriopsis,Thozetella,Thyrostroma(rela-tively poorly studied genera)and the basidiomycete genus Lepiota.We provide examples where knowledge is incomplete or lacking and suggest areas needing further research.These include(1)the need to establish what is a species,(2)the need to establish how host-specific fungi are,not in highly disturbed urban areas,but in pristine or relatively undisturbed forests,and(3)the need to establish if species in different continents,islands,countries or regions are different,or if the same fungi occur worldwide?Finally,we conclude whether we are anywhere near to flattening the curve in new species description.

Microfungi associated with Clematis(Ranunculaceae)with an integrated approach to delimiting species boundaries

The cosmopolitan plant genus Clematis contains many climbing species that can be found worldwide.The genus occurs in the wild and is grown commercially for horticulture.Microfungi on Clematis were collected from Belgium,China,Italy,Thailand and the UK.They are characterized by morphology and analyses of gene sequence data using an integrated species concept to validate identifications.The study revealed two new families,12 new genera,50 new species,26 new host records with one dimorphic character report,and ten species are transferred to other genera.The new families revealed by multigene phylogeny are Longiostiolaceae and Pseudomassarinaceae in Pleosporales(Dothideomycetes).New genera are Anthodidymella(Didymellaceae),Anthosulcatispora and Parasulcatispora(Sulcatisporaceae),Fusiformispora(Amniculicolaceae),Longispora(Phaeosphaeriaceae),Neobyssosphaeria(Melanommataceae),Neoleptosporella(Chaetosphaeriales,genera incertae sedis),Neostictis(Stictidaceae),Pseudohelminthosporium(Neomassarinaceae),Pseudomassarina(Pseudomassarinaceae),Sclerenchymomyces(Leptosphaeriaceae)and Xenoplectosphaerella(Plectosphaerellaceae).The newly described species are Alloleptosphaeria clematidis,Anthodidymella ranunculacearum,Anthosulcatispora subglobosa,Aquadictyospora clematidis,Brunneofusispora clematidis,Chaetosphaeronema clematidicola,C.clematidis,Chromolaenicola clematidis,Diaporthe clematidina,Dictyocheirospora clematidis,Distoseptispora clematidis,Floricola clematidis,Fusiformispora clematidis,Hermatomyces clematidis,Leptospora clematidis,Longispora clematidis,Massariosphaeria clematidis,Melomastia clematidis,M.fulvicomae,Neobyssosphaeria clematidis,Neoleptosporella clematidis,Neoroussoella clematidis,N.fulvicomae,Neostictis nigricans,Neovaginatispora clematidis,Parasulcatispora clematidis,Parathyridaria clematidis,P.serratifoliae,P.virginianae,Periconia verrucose,Phomatospora uniseriata,Pleopunctum clematidis,Pseudocapulatispora clematidis,Pseudocoleophoma clematidis,Pseudohelminthosporium clematidis,Pseudolophiostoma chiangraiense,P.clematidis,Pseudomassarina clematidis,Ramusculicola clematidis,Sarocladium clematidis,Sclerenchymomyces clematidis,Sigarispora clematidicola,S.clematidis,S.montanae,Sordaria clematidis,Stemphylium clematidis,Wojnowiciella clematidis,Xenodidymella clematidis,Xenomassariosphaeria clematidis and Xenoplectosphaerella clematidis.The following fungi are recorded on Clematis species for the first time:Angustimassarina rosarum,Dendryphion europaeum,Dermatiopleospora mariae,Diaporthe ravennica,D.rudis,Dichotomopilus ramosissimum,Dictyocheirospora xishuangbannaensis,Didymosphaeria rubi-ulmifolii,Fitzroyomyces cyperacearum,Fusarium celtidicola,Leptospora thailandica,Memnoniella oblongispora,Neodidymelliopsis longicolla,Neoeutypella baoshanensis,Neoroussoella heveae,Nigrograna chromolaenae,N.obliqua,Pestalotiopsis verruculosa,Pseudoberkleasmium chiangmaiense,Pseudoophiobolus rosae,Pseudoroussoella chromolaenae,P.elaeicola,Ramusculicola thailandica,Stemphylium vesicarium and Torula chromolaenae.The new combinations are Anthodidymella clematidis(≡Didymella clematidis),A.vitalbina(≡Didymella vitalbina),Anthosulcatispora brunnea(≡Neobambusicola brunnea),Fuscohypha kunmingensis(≡Plectosphaerella kunmingensis),Magnibotryascoma rubriostiolata(≡Teichospora rubriostiolata),Pararoussoella mangrovei(≡Roussoella mangrovei),Pseudoneoconiothyrium euonymi(≡Roussoella euonymi),Sclerenchymomyces jonesii(≡Neoleptosphaeria jonesii),Stemphylium rosae(≡Pleospora rosae),and S.rosae-caninae(≡Pleospora rosae-caninae).The microfungi on Clematis is distributed in several classes of Ascomycota.The analyses are based on morphological examination of specimens,coupled with phylogenetic sequence data.To the best of our knowledge,the consolidated species concept approach is recommended in validating species.

Species diversity of Basidiomycota

Fungi are eukaryotes that play essential roles in ecosystems.Among fungi,Basidiomycota is one of the major phyla with more than 40,000 described species.We review species diversity of Basidiomycota from five groups with different lifestyles or habitats:saprobic in grass/forest litter,wood-decaying,yeast-like,ectomycorrhizal,and plant parasitic.Case studies of Agaricus,Cantharellus,Ganoderma,Gyroporus,Russula,Tricholoma,and groups of lichenicolous yeast-like fungi,rust fungi,and smut fungi are used to determine trends in discovery of biodiversity.In each case study,the number of new species published during 2009–2020 is analysed to determine the rate of discovery.Publication rates differ between taxa and reflect different states of progress for species discovery in different genera.The results showed that lichenicolous yeast-like taxa had the highest publication rate for new species in the past two decades,and it is likely this trend will continue in the next decade.The species discovery rate of plant parasitic basidiomycetes was low in the past ten years,and remained constant in the past 50 years.We also found that the establishment of comprehensive and robust taxonomic systems based on a joint global initiative by mycologists could promote and standardize the recognition of taxa.We estimated that more than 54,000 species of Basidiomycota will be discovered by 2030,and estimate a total of 1.4–4.2 million species of Basidiomycota glob-ally.These numbers illustrate a huge gap between the described and yet unknown diversity in Basidiomycota.

Biphasic taxonomic approaches for generic relatedness and phylogenetic relationships of Teichosporaceae

The placement of the dothideomycetous family Teichosporaceae has been controversial.Recent phylogenetic investigations have used a taxonomic lumping approach with the Floricolaceae and its genera have been synonymized under the earlier fam-ily name,Teichosporaceae.Intergeneric relationships were therefore obscure and proper generic delimitation was needed in upcoming studies.We here taxonomically revised the family Teichosporaceae based on both morphological and phylogenetic evidence.Teichosporaceae species have immersed or semi-immersed,erumpent to superficial,ostiolate ascomata,cellular or trabeculate pseudoparaphyses,cylindrical to oblong or sub-clavate asci and ellipsoid to oblong or fusiform,cylindric-fusiform or oblong to elliptical,ovoid to clavate,symmetric or asymmetric,initially hyaline or pale brown to dark brown or yellowish brown,1-3-septate or muriform ascospores.Asexual morphs are coelomycetous.Type or representative speci-mens of Teichosporaceae were loaned and fresh specimens were collected from China and Thailand.Maximum likelihood and Bayesian analyses of a combined ITS,LSU,SSU,tef1-αand rpb2 dataset were performed to clarify the phylogenetic affinities of taxa and examine monophyly of newly proposed genera.One new species(Floricola festucae),one new host record(Ramusculicola thailandica)and four new combinations(Aurantiascoma nephelii,A.quercus,Magnibotryascoma acaciae,M.melanommoides)are introduced.The broad genus concept of Teichospora is dismissed based on morphological dissimilarities and the monophyletic status of the proposed genera.We accept Asymmetrispora,Aurantiascoma,Floricola,Magnibotryascoma,Misturatosphaeria,Pseudoaurantiascoma,Pseudomisturatosphaeria,Ramusculicola and Teichospora as distinct genera in the Teichosporaceae.All recognized genera are phenotypically characterized and phylogenetically well-supported.The phylogenetic placements of three genera(Chaetomastia,Loculohypoxylon and Sinodidymella),which do not have molecular data cannot be conclusively clarified at present,but are still placed in Teichosporaceae for future studies.

Occurrence and geographical distribution of mangrove fungi

This is a multidimensional review of mangrove fungi occurring as saprobes,pathogens and endophytes of a wide range of host substrates and those isolated from the water columns and sediments in mangroves.Eight-hundred and fifty taxa including 658 that are supported by both morphology and molecular data and 192 with only morphological data are listed.These constitute Ascomycota,the dominant group with 773 species,and 58 Basidiomycota,one Blastocladiomycota,five Chytridiomycota,and 13 Mucoromycota.This study also includes data on mangrove yeasts 103 Ascomycota,39 Basidi-omycota and 193 taxa isolated from sediments.Endophytes isolated from submerged parts of mangrove plants total 38.The most specious orders of mangrove fungi are Pleosporales 133,Saccharomycetales 102,Microascales 101,Eurotiales 87,Hypocreales 60 and Xylariales 54.Speciose genera include Candida 39,Aspergillus 53,Penicillium 17 and Corollospora 16.The highest number of mangrove fungi have been recorded from the Pacific Ocean 553,which is the largest ocean,followed by Indian 408 and Atlantic Oceans 259.Geographical distribution of mangrove fungi varied from ocean to ocean with only 109 taxa common to the Atlantic,Indian and Pacific Oceans.Of the various countries reported for mangrove fungi,India accommodates the highest number(339)followed by Thailand 303,Malaysia 171,Florida Everglades,USA 134 and Brunei 134.A total of 60 different mangrove plants and their associates have been surveyed for mangrove fungi.These results are discussed and compared with previous studies.

What is a species in fungal plant pathogens?

Scientific names are crucial for communicating knowledge concerning fungi and fungus-like organisms.In plant pathology,they link information regarding biology,host range,distribution and potential risk to agriculture and food security.In the past,delimitation among pathogenic taxa was primarily based on morphological characteristics.Due to distinct species sharing overlapping characteristics,the morphological identification of species is often neither straightforward nor reliable.Hence,the phylogenetic species concept based on molecular phylogenetic reconstructions gained importance.The present opinion discusses what a fungal species is and how identification of species in plant pathology has changed over the past decades.In this context,host-specialization and species complexes are discussed.Furthermore,species concepts in plant pathology are examined using case studies from Bipolaris,Colletotrichum,Curvularia,Diaporthe,Diplodia,Meliola,Plasmopara,rust fungi and Trichoderma.Each entry contains a brief introduction to the genus,concepts used in species identification so far and the problems in describing a species followed by recommendations.The importance of correctly naming and identifying a species is addressed in the context of recent introductions,and we also discuss whether the introduction of new species in pathogenic genera has been overestimated.We also provide guidelines to be considered when introducing a new species in a plant pathogenic genus.

Refined families of Dothideomycetes:orders and families incertae sedis in Dothideomycetes

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.

Fungal diversity notes 1387-1511:taxonomic and phylogenetic contributions on genera and species of fungal taxa

This article is the 13th contribution in the Fungal Diversity Notes series,wherein 125 taxa from four phyla,ten classes,31 orders,69 families,92 genera and three genera incertae sedis are treated,demonstrating worldwide and geographic distri-bution.Fungal taxa described and illustrated in the present study include three new genera,69 new species,one new com-bination,one reference specimen and 51 new records on new hosts and new geographical distributions.Three new genera,Cylindrotorula(Torulaceae),Scolecoleotia(Leotiales genus incertae sedis)and Xenovaginatispora(Lindomycetaceae)are introduced based on distinct phylogenetic lineages and unique morphologies.Newly described species are Aspergillus lan-naensis,Cercophora dulciaquae,Cladophialophora aquatica,Coprinellus punjabensis,Cortinarius alutarius,C.mammil-latus,C.quercoflocculosus,Coryneum fagi,Cruentomycena uttarakhandina,Cryptocoryneum rosae,Cyathus uniperidiolus,Cylindrotorula indica,Diaporthe chamaeropicola,Didymella azollae,Diplodia alanphillipsii,Dothiora coronicola,Efibula rodriguezarmasiae,Erysiphe salicicola,Fusarium queenslandicum,Geastrum gorgonicum,G.hansagiense,Helicosporium sexualis,Helminthosporium chiangraiensis,Hongkongmyces kokensis,Hydrophilomyces hydraenae,Hygrocybe boertmannii,Hyphoderma australosetigerum,Hyphodontia yunnanensis,Khaleijomyces umikazeana,Laboulbenia divisa,Laboulbenia triarthronis,Laccaria populina,Lactarius pallidozonarius,Lepidosphaeria strobelii,Longipedicellata megafusiformis,Lophiotrema lincangensis,Marasmius benghalensis,M.jinfoshanensis,M.subtropicus,Mariannaea camelliae,Mel-anographium smilaxii,Microbotryum polycnemoides,Mimeomyces digitatus,Minutisphaera thailandensis,Mortierella solitaria,Mucor harpali,Nigrograna jinghongensis,Odontia huanrenensis,O.parvispina,Paraconiothyrium ajrekarii,Par-afuscosporella niloticus,Phaeocytostroma yomensis,Phaeoisaria synnematicus,Phanerochaete hainanensis,Pleopunctum thailandicum,Pleurotheciella dimorphospora,Pseudochaetosphaeronema chiangraiense,Pseudodactylaria albicolonia,Rhexoacrodictys nigrospora,Russula paravioleipes,Scolecoleotia eriocamporesi,Seriascoma honghense,Synandromyces makranczyi,Thyridaria aureobrunnea,Torula lancangjiangensis,Tubeufia longihelicospora,Wicklowia fusiformispora,Xenovaginatispora phichaiensis and Xylaria apiospora.One new combination,Pseudobactrodesmium stilboideus is pro-posed.A reference specimen of Comoclathris permunda is designated.New host or distribution records are provided for Acrocalymma fici,Aliquandostipite khaoyaiensis,Camarosporidiella laburni,Canalisporium caribense,Chaetoscutula juniperi,Chlorophyllum demangei,C.globosum,C.hortense,Cladophialophora abundans,Dendryphion hydei,Diaporthe foeniculina,D.pseudophoenicicola,D.pyracanthae,Dictyosporium pandanicola,Dyfrolomyces distoseptatus,Ernakula-mia tanakae,Eutypa flavovirens,E.lata,Favolus septatus,Fusarium atrovinosum,F.clavum,Helicosporium luteosporum,Hermatomyces nabanheensis,Hermatomyces sphaericoides,Longipedicellata aquatica,Lophiostoma caudata,L.clematidis-vitalbae,Lophiotrema hydei,L.neoarundinaria,Marasmiellus palmivorus,Megacapitula villosa,Micropsalliota globocys-tis,M.gracilis,Montagnula thailandica,Neohelicosporium irregulare,N.parisporum,Paradictyoarthrinium diffractum,Phaeoisaria aquatica,Poaceascoma taiwanense,Saproamanita manicata,Spegazzinia camelliae,Submersispora variabi-lis,Thyronectria caudata,T.mackenziei,Tubeufia chiangmaiensis,T.roseohelicospora,Vaginatispora nypae,Wicklowia submersa,Xanthagaricus necopinatus and Xylaria haemorrhoidalis.The data presented herein are based on morphological examination of fresh specimens,coupled with analysis of phylogenetic sequence data to better integrate taxa into appropriate taxonomic ranks and infer their evolutionary relationships.

A polyphasic approach to delineate species in Bipolaris

Bipolaris species are important plant pathogens with a worldwide distribution in tropical and temperate environments.Species recognition in Bipolaris has been problematic due to a lack of molecular data from ex-type cultures,the use of few gene regions for species resolution and overlapping morphological characters.In this study,we evaluate the efficiency of different DNA barcodes in species delimitation in Bipolaris by phylogenetic analyses,Automatic Barcode Gap Discovery and Objective Clustering.GAPDH is determined to be the best single marker for the genus.These approaches are used to clarify the taxonomic placement of all sequences currently named as Bipolaris in GenBank based on ITS and GAPDH gene sequence data.In checking various publications,we found that the majority of new host records of fungal species published in the Plant Disease journal from 2010 to 2019 were based on BLAST searches of the ITS sequences and up to 82%of those records could be erroneous.Therefore,relying on BLAST searches from GenBank to name species is not recommended.Editorial boards of journals and reviewers of new record papers should be aware of this problem.In naming Bipolaris species,whether new or known,it is recommended to perform phylogenetic analyses based on GAPDH using the correct taxon sampling for accurate results and the species relationship should have reliable statistical support.At least two new species are represented by molecular data in GenBank and we provide an updated taxonomic revision of Bipolaris.We accept 45 species in Bipolaris and notes are provided for all the species including hosts and geographic distribution.

Taxonomic and phylogenetic contributions to fungi associated with the invasive weed Chromolaena odorata (Siam weed)

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.

One stop shop IV: taxonomic update with molecular phylogeny for important phytopathogenic genera: 76-100 (2020)

This is a continuation of a series focused on providing a stable platform for the taxonomy of phytopathogenic fungi and fungus-like organisms.This paper focuses on one family:Erysiphaceae and 24 phytopathogenic genera:Armillaria,Barrio-psis,Cercospora,Cladosporium,Clinoconidium,Colletotrichum,Cylindrocladiella,Dothidotthia,,Fomitopsis,Ganoderma,Golovinomyces,Heterobasidium,Meliola,Mucor,Neoerysiphe,Nothophoma,Phellinus,Phytophthora,Pseudoseptoria,Pythium,Rhizopus,Stemphylium,Thyrostroma and Wojnowiciella.Each genus is provided with a taxonomic background,distribution,hosts,disease symptoms,and updated backbone trees.Species confirmed with pathogenicity studies are denoted when data are available.Six of the genera are updated from previous entries as many new species have been described.

Appressorial interactions with host and their evolution

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.