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Context 1
... isolates were maintained on PDA medium, stored at 14 • C and transferred at 6-month intervals. Some isolates from other hosts were also included for comparisons (Table 1). ...
Context 2
... the six isolates of Rhizoctonia from Eucalyptus cut- tings with necrosis on leaves, four were multinucleate and two binucleate (Table 1). Among twelve isolates from plants or shoots with symptoms of leaf scorch col- lected in the field, eleven were multinucleate and one binucleate. ...
Context 3
... multinucleate isolates from plants with leaf scorch, and all multinucleate isolates from necrotic lesions on cuttings, anastomosed with isolates of group AG-1 of R. solani (Table 1). Multinucleate isolates RH-6, RH-8, and RH-11 from Eucalyptus, RH-7 from cotton and RH-12 from bean anastomosed with isolates from group AG-4. ...
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Citations
... Notes -Species of Falcocladium are commonly isolated from leaf litter, and considered to be weak foliar pathogens of Eucalyptus (Crous et al. 1994(Crous et al. , 1997(Crous et al. , 2018a. Five species are presently known, having been collected on eucalypt leaves in Africa, Asia, Australia and South America. ...
Novel species of fungi described in this study include those from various countries as follows: Antarctica , Apenidiella antarctica from permafrost, Cladosporium fildesense from an unidentified marine sponge. Argentina , Geastrum wrightii on humus in mixed forest. Australia , Golovinomyces glandulariae on Glandularia aristigera , Neoanungitea eucalyptorum on leaves of Eucalyptus grandis , Teratosphaeria corymbiicola on leaves of Corymbia ficifolia , Xylaria eucalypti on leaves of Eucalyptus radiata . Brazil , Bovista psammophila on soil, Fusarium awaxy on rotten stalks of Zea mays , Geastrum lanuginosum on leaf litter covered soil, Hermetothecium mikaniae-micranthae (incl. Hermetothecium gen. nov.) on Mikania micrantha , Penicillium reconvexovelosoi in soil, Stagonosporopsis vannaccii from pod of Glycine max . British Virgin Isles , Lactifluus guanensis on soil. Canada , Sorocybe oblongispora on resin of Picea rubens . Chile , Colletotrichum roseum on leaves of Lapageria rosea . China , Setophoma caverna from carbonatite in Karst cave. Colombia , Lareunionomyces eucalypticola on leaves of Eucalyptus grandis . Costa Rica , Psathyrella pivae on wood. Cyprus , Clavulina iris on calcareous substrate. France , Chromosera ambigua and Clavulina iris var. occidentalis on soil. French West Indies , Helminthosphaeria hispidissima on dead wood. Guatemala , Talaromyces guatemalensis in soil. Malaysia , Neotracylla pini (incl. Tracyllales ord. nov. and Neotracylla gen. nov.) and Vermiculariopsiella pini on needles of Pinus tecunumanii . New Zealand , Neoconiothyrium viticola on stems of Vitis vinifera , Parafenestella pittospori on Pittosporum tenuifolium , Pilidium novae-zelandiae on Phoenix sp. Pakistan , Russula quercus-floribundae on forest floor. Portugal , Trichoderma aestuarinum from saline water. Russia , Pluteus liliputianus on fallen branch of deciduous tree, Pluteus spurius on decaying deciduous wood or soil. South Africa , Alloconiothyrium encephalarti , Phyllosticta encephalarticola and Neothyrostroma encephalarti (incl. Neothyrostroma gen. nov.) on leaves of Encephalartos sp., Chalara eucalypticola on leaf spots of Eucalyptus grandis × urophylla , Clypeosphaeria oleae on leaves of Olea capensis , Cylindrocladiella postalofficium on leaf litter of Sideroxylon inerme , Cylindromonium eugeniicola (incl. Cylindromonium gen. nov.) on leaf litter of Eugenia capensis , Cyphellophora goniomatis on leaves of Gonioma kamassi , Nothodactylaria nephrolepidis (incl. Nothodactylaria gen. nov. and Nothodactylariaceae fam. nov.) on leaves of Nephrolepis exaltata , Falcocladium eucalypti and Gyrothrix eucalypti on leaves of Eucalyptus sp., Gyrothrix oleae on leaves of Olea capensis subsp. macrocarpa , Harzia metrosideri on leaf litter of Metrosideros sp., Hippopotamyces phragmitis (incl. Hippopotamyces gen. nov.) on leaves of Phragmites australis , Lectera philenopterae on Philenoptera violacea , Leptosillia mayteni on leaves of Maytenus heterophylla , Lithohypha aloicola and Neoplatysporoides aloes on leaves of Aloe sp., Millesimomyces rhoicissi (incl. Millesimomyces gen. nov.) on leaves of Rhoicissus digitata , Neodevriesia strelitziicola on leaf litter of Strelitzia nicolai , Neokirramyces syzygii (incl. Neokirramyces gen. nov.) on leaf spots of Syzygium sp., Nothoramichloridium perseae (incl. Nothoramichloridium gen. nov. and Anungitiomycetaceae fam. nov.) on leaves of Persea americana , Paramycosphaerella watsoniae on leaf spots of Watsonia sp., Penicillium cuddlyae from dog food, Podocarpomyces knysnanus (incl. Podocarpomyces gen. nov.) on leaves of Podocarpus falcatus , Pseudocercospora heteropyxidicola on leaf spots of Heteropyxis natalensis , Pseudopenidiella podocarpi , Scolecobasidium podocarpi and Ceramothyrium podocarpicola on leaves of Podocarpus latifolius , Scolecobasidium blechni on leaves of Blechnum capense , Stomiopeltis syzygii on leaves of Syzygium chordatum , Strelitziomyces knysnanus (incl. Strelitziomyces gen. nov.) on leaves of Strelitzia alba , Talaromyces clemensii from rotting wood in goldmine, Verrucocladosporium visseri on Carpobrotus edulis . Spain , Boletopsis mediterraneensis on soil, Calycina cortegadensisi on a living twig of Castanea sativa , Emmonsiellopsis tuberculata in fluvial sediments, Mollisia cortegadensis on dead attached twig of Quercus robur , Psathyrella ovispora on soil, Pseudobeltrania lauri on leaf litter of Laurus azorica , Terfezia dunensis in soil, Tuber lucentum in soil, Venturia submersa on submerged plant debris. Thailand , Cordyceps jakajanicola on cicada nymph, Cordyceps kuiburiensis on spider, Distoseptispora caricis on leaves of Carex sp., Ophiocordyceps khonkaenensis on cicada nymph. USA , Cytosporella juncicola and Davidiellomyces juncicola on culms of Juncus effusus , Monochaetia massachusettsianum from air sample, Neohelicomyces melaleucae and Periconia neobrittanica on leaves of Melaleuca styphelioides × lanceolata , Pseudocamarosporium eucalypti on leaves of Eucalyptus sp., Pseudogymnoascus lindneri from sediment in a mine, Pseudogymnoascus turneri from sediment in a railroad tunnel, Pulchroboletus sclerotiorum on soil, Zygosporium pseudomasonii on leaf of Serenoa repens . Vietnam , Boletus candidissimus and Veloporphyrellus vulpinus on soil. Morphological and culture characteristics are supported by DNA barcodes.
... On MEA, PDA and OA surface dirty white to buff, reverse buff. Notes -Falcocladium represents a genus of hyphomycetes associated with leaf litter, or considered to be weak foliar pathogens of Eucalyptus (Crous et al. 1994(Crous et al. , 1997. Four species are presently known in the genus, having been collected on eucalypt leaves in Asia, Australia and South America. ...
Novel species of fungi described in this study include those from various countries as follows: Angola, Gnomoniopsis angolensis and Pseudopithomyces angolensis on unknown host plants. Australia, Dothiora corym biae on Corymbia citriodora, Neoeucasphaeria eucalypti (incl. Neoeucasphaeria gen. nov.) on Eucalyptus sp., Fumagopsis stellae on Eucalyptus sp., Fusculina eucalyptorum (incl. Fusculinaceae fam. nov.) on Eucalyptus socialis, Harknessia corymbiicola on Corymbia maculata, Neocelosporium eucalypti (incl. Neocelosporium gen. nov., Neocelosporiaceae fam. nov. and Neocelosporiales ord. nov.) on Eucalyptus cyanophylla, Neophaeomoniella corymbiae on Corymbia citriodora, Neophaeomoniella eucalyptigena on Eucalyptus pilularis, Pseudoplagiostoma corymbiicola on Corymbia citriodora, Teratosphaeria gracilis on Eucalyptus gracilis, Zasmidium corymbiae on Corymbia citriodora. Brazil, Calonectria hemileiae on pustules of Hemileia vastatrix formed on leaves of Coffea arabica, Calvatia caatinguensis on soil, Cercospora solanibetacei on Solanum betaceum, Clathrus natalensis on soil, Diaporthe poincianellae on Poincianella pyramidalis, Geastrum piquiriunense on soil, Geosmithia carolliae on wing of Carollia perspicillata, Henningsia resupinata on wood, Penicillium guaibinense from soil, Periconia caespitosa from leaf litter, Pseudocercospora styracina on Styrax sp., Simplicillium filiforme as endophyte from Citrullus lanatus, Thozetella pindobacuensis on leaf litter, Xenosonderhenia coussapoae on Coussapoa floccosa. Canary Islands (Spain), Orbilia amarilla on Euphorbia canariensis. Cape Verde Islands, Xylodon jacobaeus on Eucalyptus camaldulensis. Chile, Colletotrichum arboricola on Fuchsia magellanica. Costa Rica, Lasiosphaeria miniovina on tree branch. Ecuador, Ganoderma chocoense on tree trunk. France, Neofitzroyomyces nerii (incl. Neofitzroyomyces gen. nov.) on Nerium oleander. Ghana, Castanediella tereticornis on Eucalyptus tereticornis, Falcocladium africanum on Eucalyptus brassiana, Rachicladosporium corymbiae on Corymbia citriodora. Hungary, Entoloma silvaefrondosae in Carpinus betulus-Pinus sylvestris mixed forest. Iran, Pseudopyricularia persiana on Cyperus sp. Italy, Inocybe roseascens on soil in mixed forest. Laos, Ophiocordyceps houaynhangensis on Coleoptera larva. Malaysia, Monilochaetes melastomae on Melastoma sp. Mexico, Absidia terrestris from soil. Netherlands, Acaulium pannemaniae, Conioscypha boutwelliae, Fusicolla septimanifiniscientiae, Gibellulopsis simonii, Lasionectria hilhorstii, Lectera nordwiniana, Leptodiscella rintelii, Parasarocladium debruynii and Saro cladium dejongiae (incl. Sarocladiaceae fam. nov.) from soil. New Zealand, Gnomoniopsis rosae on Rosa sp. and Neodevriesia metrosideri on Metrosideros sp. Puerto Rico, Neodevriesia coccolobae on Coccoloba uvifera, Neodevriesia tabebuiae and Alfaria tabebuiae on Tabebuia chrysantha. Russia, Amanita paludosa on bogged soil in mixed deciduous forest, Entoloma tiliae in forest of Tilia × europaea, Kwoniella endophytica on Pyrus communis. South Africa, Coniella diospyri on Diospyros mespiliformis, Neomelanconiella combreti (incl. Neomelanconiellaceaefam. nov. and Neomelanconiella gen. nov.) on Combretum sp., Polyphialoseptoria natalensis on unidentified plant host, Pseudorobillarda bolusanthi on Bolusanthus speciosus, Thelonectria pelargonii on Pelargonium sp. Spain, Vermiculariopsiella lauracearum and Anungitopsis lauri on Laurus novocanariensis, Geosmithia xerotolerans from a darkened wall of a house, Pseudopenidiella gallaica on leaf litter. Thailand, Corynespora thailandica on wood, Lareunionomyces loeiensis on leaf litter, Neocochlearomyces chromolaenae (incl. Neocochlearomyces gen. nov.) on Chromolaena odorata, Neomyrmecridium septatum (incl. Neomyrmecridium gen. nov.), Pararamichloridium caricicola on Carex sp., Xenodactylaria thailandica (incl. Xenodactylariaceae fam. nov. and Xenodactylaria gen. nov.), Neomyrmecridium asiaticum and Cymostachys thailandica from unidentified vine. USA, Carolinigaster bonitoi (incl. Carolinigaster gen. nov.) from soil, Penicillium fortuitum from house dust, Phaeotheca shathenatiana (incl. Phaeothecaceae fam. nov.) from twig and cone litter, Pythium wohlseniorum from stream water, Superstratomyces tardicrescens from human eye, Talaromyces iowaense from office air. Vietnam, Fistulinella olivaceoalba on soil. Morphological and culture characteristics along with DNA barcodes are provided.
... The or der Diaporthales is characterized by perithecia with an elongate beak, often formingwithin stromatic tissues (Rossman et al. 2007 This monotypic order in the subclass Hypocreomycetidae is introduced to accommodate the family Falcocladiaceae. Members of this family are saprobes on leaf litter and leaves including Eucalyptus grandis and E. camaldulensis in tropical, terrestrial habitats (Crous et al. 1994;Jones et al. 2014). Sexual morph: Undetermined. ...
... Notes: The order presently includes one hyphomycetous asexual genus Falcocladium introduced by Crous et al. (1994). Jones et al. (2014) introduced the monotypic family Falcocladiaceae based on SSU and LSU sequence data to accommodate the members of genus Falcocladium and suggested further taxon sampling was needed to determine its ordinal status. ...
Sordariomycetesis one of the largest classes of Ascomycota
and is characterised by perithecial ascomata and inoperculate
unitunicate asci. The class includes many important plant
pathogens, as well as endophytes, saprobes, epiphytes, and
fungicolous, lichenized or lichenicolous taxa. The class includes freshwater, marine and terrestrial taxa and has a
worldwide distribution. This paper provides an updated outline of theSordariomycetesand a backbone tree incorporating
asexual and sexual genera in the class. Based on phylogeny
and morphology we introduced three subclasses;
Diaporthomycetidae, Lulworthiomycetidaeand
Meliolomycetidaeand five orders;Amplistromatales,
Annulatascales, Falcocladiales, Jobellisiales and Togniniales. The outline is based on literature to the end of
2014 and the backbone tree published in this paper. Notes for
397 taxa with information, such as new family and genera
novelties, novel molecular data published since the Outline
of Ascomycota 2009, and new links between sexual and asexual genera and thus synonymies, are provided. The Sordariomycetes now comprises six subclasses, 28 orders,
90 families and 1344 genera. In addition a list of 829 genera
with uncertain placement in Sordariomycetesis also provided.
... Silveira, Alfenas, Crous & M.J. Wingf. (Crous et al. 1994), F. sphaeropedunculatum (Crous et al. 1997), F. thailandicum Crous & Himaman (Crous et al. 2007) e F. turbinatum Somrithipol, Sudhom, Tippawan & E.B.G. Jones (Somrithipol et al. 2007). ...
Um inventário de fungos conidiais foi realizado em seis áreas de extrema importância biológica no bioma Caatinga. Foram coletadas 74 espécies, sendo sete novos registros para o Brasil. Heliocephala zimbabweensis Decock, V. Robert & Masuka é reportada pela segunda vez para a ciência, Sporidesmium verrucisporum M.B. Ellis é um novo registro para o continente americano, Dicyma vesiculifera Piroz., Fusariella concinna (Syd.) S. Hughes, F. obstipa (Pollack) S. Hughes, Phaeostalagmus tenuissimus (Corda) W. Gams e Sporidesmiella claviformis P.M. Kirk são novos registros para a América do Sul. Falcocladium sphaeropedunculatum Crous & Alfenas, Myrmecridium schulzeri var. schulzeri (Sacc.) Arzanlou, W. Gams & Crous, Pseudodictyosporium wauense Matsush., Repetophragma inflatum (Berk. & Ravenel) W.P. Wu são novos registros para o semi-árido brasileiro. Seis espécies foram reconhecidas como novos taxa, Brachysporiellina fecunda S.M. Leão, A.C. Cruz, R.F. Castañeda & Gusmão, Diplococcium verruculosum A.C. Cruz, Gusmão & R.F. Castañeda, Lobatopedis longistriatum A.C. Cruz, Gusmão, S.M. Leão-Ferreira & R.F. Castañeda, Subramaniomyces pulcher A.C. Cruz, Gusmão & R.F. Castañeda e foram publicadas separadamente. Os novos registros são descritos, ilustrados e comentados. Uma lista incluindo as demais espécies encontradas é apresentada.
... Silveira, Alfenas, Crous & M.J. Wingf. (Crous et al. 1994), F. sphaeropedunculatum (Crous et al. 1997), F. thailandicum Crous & Himaman (Crous et al. 2007) e F. turbinatum Somrithipol, Sudhom, Tippawan & E.B.G. Jones (Somrithipol et al. 2007). ...
Um inventário de fungos conidiais foi realizado em seis áreas de extrema importância biológica no bioma Caatinga. Foram coletadas 74 espécies, sendo sete novos registros para o Brasil. Heliocephala zimbabweensis Decock, V. Robert & Masuka é reportada pela segunda vez para a ciência, Sporidesmium verrucisporum M.B. Ellis é um novo registro para o continente americano, Dicyma vesiculifera Piroz., Fusariella concinna (Syd.) S. Hughes, F. obstipa (Pollack) S. Hughes, Phaeostalagmus tenuissimus (Corda) W. Gams e Sporidesmiella claviformis P.M. Kirk são novos registros para a América do Sul. Falcocladium sphaeropedunculatum Crous & Alfenas, Myrmecridium schulzeri var. schulzeri (Sacc.) Arzanlou, W. Gams & Crous, Pseudodictyosporium wauense Matsush., Repetophragma inflatum (Berk. & Ravenel) W.P. Wu são novos registros para o semi-árido brasileiro. Seis espécies foram reconhecidas como novos taxa, Brachysporiellina fecunda S.M. Leão, A.C. Cruz, R.F. Castañeda & Gusmão, Diplococcium verruculosum A.C. Cruz, Gusmão & R.F. Castañeda, Lobatopedis longistriatum A.C. Cruz, Gusmão, S.M. Leão-Ferreira & R.F. Castañeda, Subramaniomyces pulcher A.C. Cruz, Gusmão & R.F. Castañeda e foram publicadas separadamente. Os novos registros são descritos, ilustrados e comentados. Uma lista incluindo as demais espécies encontradas é apresentada.
... This character has not been reported from cheirosporous genera. Similar sterile branches occur among conidiophores in species of genera such as Cylindrocladium, Falcocladium, Vesicladiella and Tubercularia, and in the first three, sterile branches have been regarded as a diagnostic generic character (Seifert 1985, Crous & Wingfield 1994, Crous et al. 1994). ...
Cheirosporium gen. nov. is characterised by the production of sporodochial conidiomata, semi-macronematous to macronematous conidiophores that possess several distinct sterile branches, and cheiroid, smooth-walled conidia with rhexolytic secession. The 28S rDNA and ITS rDNA operon of this taxon were amplified and sequenced. A BLAST search revealed low homology between Cheirosporium triseriale and existing sequences in public databases, supporting the hypothesis that the species is new to science. Phylogenetic analysis showed that C. triseriale groups with Dictyosporium and allied species, and nests within the Pleosporales (Dothideomycetes, Ascomycota). Cheirosporium is morphologically distinct from the cheirosporous genera Cheiromyces, Cheiromycina, Dictyosporium, Digitomyces, Digitodesmium and Pseudodictyosporium and these differences are discussed.
... Silveira and co-workers (in Crous et al. 1994) erected the new anamorph genus Falcocladium S.F. Silveira, Alfenas, Crous & M.J. Wingf., with Falcocladium multivesiculatum S.F. ...
The hyphomycete genus Falcocladium is reviewed. Falcocladium turbinatum, collected on dead leaves in a tropical forest in Thailand, is illustrated, described as a new species and compared with related taxa. The new fungus differs from the two previously described species of the genus by its turbinate vesicles.
Calonectria represents a genus of phytopathogenic ascomycetous fungi with a worldwide distribution. In recent years, there has been an increase in the number of taxonomic studies on these fungi. Currently, there are 169 described species of Calonectria based on comparisons of DNA sequence data, combined with morphological characteristics. However, for some of these species, the sequence data utilised at the time of their description were relatively limited. This has justified an urgent need to reconsider the species boundaries for Calonectria based on robust genus-wide phylogenetic analyses. In this study, we utilised 240 available isolates including the ex-types of 128 Calonectria species, and re-sequenced eight gene regions (act, cmdA, his3, ITS, LSU, rpb2, tef1 and tub2) for them. Sequences for 44 Calonectria species, for which cultures could not be obtained, were downloaded from GenBank. DNA sequence data of all the 169 Calonectria species were then used to determine their phylogenetic relationships. As a consequence, 51 species were reduced to synonymy, two new species were identified, and the name Ca. lauri was validated. This resulted in the acceptance of 120 clearly defined Calonectria spp. The overall data revealed that the genus includes 11 species complexes, distributed across the Prolate and Sphaero-Naviculate Groups known to divide Calonectria. The results also made it possible to develop a robust set of DNA barcodes for Calonectria spp. To accomplish this goal, we evaluated the outcomes of each of the eight candidate DNA barcodes for the genus, as well as for each of the 11 species complexes. No single gene region provided a clear identity for all Calonectria species. Sequences of the tef1 and tub2 genes were the most reliable markers; those for the cmdA, his3, rpb2 and act gene regions also provided a relatively effective resolution for Calonectria spp., while the ITS and LSU failed to produce useful barcodes for species discrimination. At the species complex level, results showed that the most informative barcodes were inconsistent, but that a combination of six candidate barcodes (tef1, tub2, cmdA, his3, rpb2 and act) provided stable and reliable resolution for all 11 species complexes. A six-gene combined phylogeny resolved all 120 Calonectria species, and revealed that tef1, tub2, cmdA, his3, rpb2 and act gene regions are effective DNA barcodes for Calonectria.
Index Fungorum, Species Fungorum and MycoBank are the key fungal nomenclature and taxonomic databases that can be sourced to find taxonomic details concerning fungi, while DNA sequence data can be sourced from the NCBI, EBI and UNITE databases. Nomenclature and ecological data on freshwater fungi can be accessed on http://fungi.life.illinois.edu/, while http://www.marinespecies.org/provides a comprehensive list of names of marine organisms, including information on their synonymy. Previous websites however have little information on marine fungi and their ecology, beside articles that deal with marine fungi, especially those published in the nineteenth and early twentieth centuries may not be accessible to those working in third world countries. To address this problem, a new website www.marinefungi.org was set up and is introduced in this paper. This website provides a search facility to genera of marine fungi, full species descriptions, key to species and illustrations, an up to date classification of all recorded marine fungi which includes all fungal groups (Ascomycota, Basidiomycota, Blastocladiomycota, Chytridiomycota, Mucoromycota and fungus-like organisms e.g. Thraustochytriales), and listing recent publications. Currently, 1257 species are listed in the marine fungi website (www.marinefungi.org), in 539 genera, 74 orders, 168 families, 20 classes and five phyla, with new taxa continuing to be described. The website has curators with specialist mycological expertise who help to provide update data on the classification of marine fungi. This article also reviews knowledge of marine fungi covering a wide range of topics: their higher classification, ecology and world distribution, role in energy transfer in the oceans, origin and new chemical structures. An updated classification of marine fungi is also included. We would like to invite all mycologists to contribute to this innovative website.
Sordariomycetes is one of the largest classes of Ascomycota that comprises a highly diverse range of fungi characterized mainly by perithecial ascomata and inoperculate unitunicate asci. The class includes many important plant pathogens, as well as endophytes, saprobes, epiphytes, coprophilous and fungicolous, lichenized or lichenicolous taxa. They occur in terrestrial, freshwater and marine habitats worldwide. This paper reviews the 107 families of the class Sordariomycetes and provides a modified backbone tree based on phylogenetic analysis of four combined loci, with a maximum five representative taxa from each family, where available. This paper brings together for the first time, since Barrs’ 1990 Prodromus, descriptions, notes on the history, and plates or illustrations of type or representative taxa of each family, a list of accepted genera, including asexual genera and a key to these taxa of Sordariomycetes. Delineation of taxa is supported where possible by molecular data. The outline is based on literature to the end of 2015 and the Sordariomycetes now comprises six subclasses, 32 orders, 105 families and 1331 genera. The family Obryzaceae and Pleurotremataceae are excluded from the class.
