Families of Sordariomycetes

Maharachchikumbura, Sajeewa S. N.; Hyde, Kevin D.; Jones, E. B. Gareth; McKenzie, Eric H. C.; Bhat, Jayarama D.; Dayarathne, Monika C.; Huang, Shi Ke; Norphanphoun, Chada; Senanayake, Indunil C.; Perera, Rekhani H.; Shang, Qiu Ju; Xiao, Yuan-Pin; D’souza, Melvina J.; Hongsanan, Sinang; Jayawardena, Ruvishika S.; Daranagama, Dinushani A.; Konta, Sirinapa; Goonasekara, Ishani D.; Zhuang, Wen; Jeewon, Rajesh; Phillips, Alan J. L.; Abdel-Wahab, Mohamed A.; Al-Sadi, Abdullah M.; Bahkali, Ali H.; Boonmee, Saranyaphat; Boonyuen, Nattawut; Cheewangkoon, Ratchadawan; Dissanayake, Asha J.; Kang, Ji-Chuan; Li, Qi Rui; Liu, Jian‐Kui; Liu, Xing Zhong; Liu, Zuo Yi; Luangsa‐ard, J. Jennifer; Pang, Ka Lai; Phookamsak, Rungtiwa; Promputtha, Itthayakorn; Suetrong, Satinee; Stadler, Marc; Wen, Ting‐Chi; Wijayawardene, Nalin N.

doi:10.1007/s13225-016-0369-6

Cited by 298 publications

(268 citation statements)

References 383 publications

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“…Accordingly, Senanayake et al (2015) placed Lopadostoma and Creosphaeria in the new family Lopadostomataceae, which was confirmed in a subsequent study by Jaklitsch et al (2016). Concurrently and subsequently, several other studies have been initiated in order to classify the non-stromatic taxa of the Xylariales (Jaklitsch and Voglmayr 2012;Daranagama et al 2015Daranagama et al , 2016Maharachchikumbura et al 2016), sometimes resulting in incongruent concepts according to the standpoint of the authors.…”

Section: Introductionmentioning

confidence: 99%

Resurrection and emendation of the Hypoxylaceae, recognised from a multigene phylogeny of the Xylariales

et al. 2017

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A multigene phylogeny was constructed, including a significant number of representative species of the main lineages in the Xylariaceae and four DNA loci the internal transcribed spacer region (ITS), the large subunit (LSU) of the nuclear rDNA, the second largest subunit of the RNA polymerase II (RPB2), and beta-tubulin (TUB2). Specimens were selected based on more than a decade of intensive morphological and chemotaxonomic work, and cautious taxon sampling was performed to cover the major lineages of the Xylariaceae; however, with emphasis on hypoxyloid species. The comprehensive phylogenetic analysis revealed a clear-cut segregation of the Xylariaceae into several major clades, which was well in accordance with previously established morphological and chemotaxonomic concepts. One of these clades contained Annulohypoxylon, Hypoxylon, Daldinia, and other related genera that have stromatal pigments and a nodulisporium-like anamorph. They are accommodated in the family Hypoxylaceae, which is resurrected and emended. Representatives of genera with a nodulisporium-like anamorph and bipartite stromata, lacking stromatal pigments (i.e. Biscogniauxia, Camillea, and Obolarina) appeared in a clade basal to the xylarioid taxa. As they clustered with Graphostroma platystomum, they are accommodated in the Graphostromataceae. The new genus Jackrogersella with J. multiformis as type species is segregated from Annulohypoxylon. The genus Pyrenopolyporus is resurrected for Hypoxylon polyporus and allied species. The genus Daldinia and its allies Entonaema, Rhopalostroma, Ruwenzoria, and Thamnomyces appeared in two separate subclades, which may warrant further splitting of Daldinia in the future, and even Hypoxylon was divided in several clades. However, more species of these genera need to be studied before a conclusive taxonomic rearrangement can be envisaged. Epitypes were designated for several important species in which living cultures and molecular data are available, in order to stabilise the taxonomy of the Xylariales.

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Section: Introductionmentioning

confidence: 99%

Resurrection and emendation of the Hypoxylaceae, recognised from a multigene phylogeny of the Xylariales

et al. 2017

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“…Colletotrichum is comprised mainly of pathogens, 74 but some species are endophytes or saprotrophs (Hyde et al 2014, Jayawardena et al 2016b). Kirk et al (2001Kirk et al ( , 2008, Réblová et al (2011) placed Colletotrichum in Glomerellaceae and this placement was confirmed by Maharachchikumbura et al (2016a). We provide accounts for C. dematium, C. godetiae, C. hebeiense, C. siamense, C. truncatum and C. viniferum based on morphology and multigene phylogenetic analysis.…”

Section: Coniella Vitismentioning

confidence: 58%

Mycosphere Notes 102–168: Saprotrophic fungi on Vitis in China, Italy, Russia and Thailand

Jayawardena¹,

Hyde²,

Chethana³

et al. 2018

Mycosphere

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This is the third paper in the series, Mycosphere notes, wherein we provide notes on various fungal taxa. In this set of notes, we deal with species found on the grape genus, Vitis, one of the most important economically important crops, grown worldwide. We provide notes on 67 taxa, including two new species, Alternaria italica and Alfaria vitis, an asexual morph for Alfaria cyperiesculenti and 41 new host records or distribution records. The taxonomic placement of most taxa discussed in this study is based on a modern taxonomic framework based on analysis of multi-gene sequence data.

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“…LSU phylogenetic analysis by Huhndorf et al (2009) indicate that Amplistromataceae has no close relationship with Chaetosphaeriales or Magnaporthaceae. In phylogenetic analyses of Maharachchikumbura et al (2015Maharachchikumbura et al ( , 2016) Amplistromatales appears to be distantly related to Meliolomycetidae and Sordariomycetidae and thus were referred to the Sordariomycetes order incertae sedis. Maharachchikumbura et al (2015) introduced a separate order, Amplistromatales, comprising two families, Amplistromataceae and Catabotrydaceae.…”

Section: Discussionmentioning

confidence: 99%

Towards a natural classification of Amplistromataceae

Daranagama¹

2017

Mycosphere

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In this study, we revise the family Amplistromataceae (Amplistromatales) based on DNA sequence data derived from living cultures and morphological observation of type and additional specimens from herbaria worldwide. Combined analyses of ITS and LSU sequence data were used to reconstruct phylogenetic relationships of members for the family. We accept three genera; Acidothrix, Amplistroma and Wallrothiella in Amplistromataceae based on the morphology and phylogeny. Modern descriptions and illustrations are provided with notes and a key to the genera is provided.

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Families of Sordariomycetes

Cited by 298 publications

References 383 publications

Resurrection and emendation of the Hypoxylaceae, recognised from a multigene phylogeny of the Xylariales

Resurrection and emendation of the Hypoxylaceae, recognised from a multigene phylogeny of the Xylariales

Mycosphere Notes 102–168: Saprotrophic fungi on Vitis in China, Italy, Russia and Thailand

Towards a natural classification of Amplistromataceae

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