Monika C. Dayarathne

Towards a natural classification and backbone tree for Sordariomycetes

Sordariomycetes is 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 the Sordariomycetes and a backbone tree incorporating asexual and sexual genera in the class. Based on phylogeny and morphology we introduced three subclasses; Diaporthomycetidae, Lulworthiomycetidae and Meliolomycetidae and 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 Sordariomycetes is also provided.

Families of Sordariomycetes

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.

Towards unraveling relationships in Xylariomycetidae (Sordariomycetes)

The classification of subclass Xylariomycetidae is revisited with additional collections and phylogeny based on novel rDNA sequence data. Phylogenetic inferences are provided and are based on analysis of 115 sequence data, including new data for 27 strains. An updated outline to the subclass is presented based on the phylogenies and comprises two orders, 18 families and 222 genera. An account of each order, family and genus in the subclass is given. We accept the orders Amphisphaeriales and Xylariales based on morphological and phylogenetic evidence. Amphisphaeriales comprises Amphisphaeriaceae, Bartaliniaceae fam. nov., Clypeosphaeriaceae, Discosiaceae fam. nov., Pestalotiopsidaceae fam. nov. and Phlogicylindriaceae fam. nov. Xylariales comprises Apiosporaceae, Cainiaceae, Coniocessiaceae, Diatrypaceae, Graphostromataceae (doubtful), Hyponectriaceae, Iodosphaeriaceae, Lopadostomaceae fam. nov., Melogrammataceae, Pseudomassariaceae fam. nov., Vialaeaceae and Xylariaceae. The new genera and species introduced are Arthrinium hyphopodii, A. subglobosa, Cainia anthoxanthis, Ciferriascosea gen. nov., C. fluctamurum, C. rectamurum, Discosia neofraxinea, D. pseudopleurochaeta, Hyalotiella rubi, Seimatosporium cornii, S. ficeae, S. vitis and Truncatella spartii.

New saprobic marine fungi and a new combination

Abstract This paper documents five new saprobic marine fungi occurring on various substrata in the marine environment. Bacusphaeria nypae gen. et sp. nov. was discovered on bases of fronds of Nypa fruticans in Malaysia and phylogenetically, it belongs to the Tirisporellaceae (Tirisporellales, Diaporthomycetidae, Sordariomycetes) based on 18S and 28S rDNA. Cryptovalsa avicenniae, Ceriosporopsis minuta and Jattaea mucronata also belong to the Sordariomycetes; Cr. avicenniae was saprobic on Avicennia marina collected in Saudi Arabia, J. mucronata on intertidal decaying bark of Rhizophora mucronata while Ce. minuta was found on driftwood collected on a sandy beach in Japan. Phylogeny based on 18S and 28S rDNA placed Cr. avicenniae with other Cryptovalsa species in the Diatrypaceae. Jattaea mucronata groups well in the Calosphaeriales and is closely related to J. algeriensis based on a phylogeny using ITS and 28S rRNA and RPB2 genes. Aegeanispora elanii gen. et sp. nov. is an asexual fungus which produces pycnidia on decaying driftwood collected in the Aegean Sea. Combined 18S and 28S rDNA phylogenetic analyses suggest that it is a member of the Pleosporales, Dothideomycetes. Ceriosporopsis minuta resembles C. capillacea with its tubular, long polar appendages of ascospores but dimensions of ascomata and ascospores for the former species are considerably smaller. Ceriosporopsis is considered the best genus to accommodate C. minuta without support from sequence data. Sammeyersia is established as a new genus to accommodate Lulworthia grandispora, a species unrelated to Lulworthia fucicola, the type species. The diagnostic characteristic for the genus is a melanized region at the base of the neck of the ascomata.

A novel marine genus, Halobyssothecium (Lentitheciaceae) and epitypification of Halobyssothecium obiones comb. nov.

A novel marine genus, Halobyssothecium (Lentitheciaceae), is introduced to accommodate Byssothecium obiones (= Halobyssothecium obiones) with evidence from phylogenetic analyses of concatenated LSU, SSU, ITS rDNA, and TEF1 sequence data. We could not locate any type material for this species and there is no molecular data available for the type of this species. Therefore, an epitype is designated for the precise delineation of this taxon. A detailed morphological description and DNA characterization based on LSU, SSU, ITS rDNA, and TEF1 sequence data are provided for the epitype, obtained from Spartina culms in Eastney, Langstone Harbour, Hampshire, UK.