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zenodo32/100

FIGURE 2 in Phaeoisaria ellipsoidea (Pleurotheciaceae, Pleurotheciales, Sordariomycetes), a new lignicolous freshwater fungus from Xishuangbanna, Yunnan Province, China

FIGURE 2. Phaeoisaria ellipsoidea (IFRD 9462, holotype) a, b Colonies on the natural substratum. c, d Conidiophores with conidia. e, f Conidiogenous cells bearing conidia. g–n Conidia. o Colony on PDA (from front). p Colony on PDA (from reverse). Scale bars: c = 50 μm, d = 80 μm, e = 10 μm, f–n = 2 μm.

opennotspecifiedMar 2023View details →
zenodo28/100

Supplementary material 1 from: Strzałka B, Jankowiak R, Bilański P, Patel N, Hausner G, Linnakoski R, Solheim H (2020) Two new species of Ophiostomatales (Sordariomycetes) associated with the bark beetle Dryocoetes alni from Poland. MycoKeys 68: 23-48. https://doi.org/10.3897/mycokeys.68.50035

Tables S1–S3

opencc-zeroJun 2020View details →
zenodo28/100

Figure 6 from: Strzałka B, Jankowiak R, Bilański P, Patel N, Hausner G, Linnakoski R, Solheim H (2020) Two new species of Ophiostomatales (Sordariomycetes) associated with the bark beetle Dryocoetes alni from Poland. MycoKeys 68: 23-48. https://doi.org/10.3897/mycokeys.68.50035

Figure 6 Leptographium alneum sp. nov. (CBS 144901) aDryocoetes alni-infested Populus tremula tree b galleries of D. alni with ascomata c ascoma d ascomatal base e ascospores f ostiolar hyphae g–i conidiophores, black arrow indicates barrel-shaped cells j conidiogenous k conidia l club-shape cells m fourteen-day-old culture on MEA. Scale bars: 50 μm (c), 25 μm (d), 10 μm (e), 10 μm (f), 25 μm (g), 25 μm (h), 50 μm (i), 10 μm (j), 10 μm (k), 50 μm (l).

opencc-by-4.0Jun 2020View details →
zenodo28/100

Figure 5 from: Strzałka B, Jankowiak R, Bilański P, Patel N, Hausner G, Linnakoski R, Solheim H (2020) Two new species of Ophiostomatales (Sordariomycetes) associated with the bark beetle Dryocoetes alni from Poland. MycoKeys 68: 23-48. https://doi.org/10.3897/mycokeys.68.50035

Figure 5 Ceratocystiopsis synnemata sp. nov. (NRIF 16918DA=KFL 16918DA) a, b micronematous conidiophores c–e macronematous conidiophores f, g conidiophores aggregate in synnematah conidia i fourteen-day-old culture on MEA. Scale bars: 25 μm (a), 10 μm (b), 25 μm (c–g), 10 μm (h).

opencc-by-4.0Jun 2020View details →
zenodo28/100

Figure 4 from: Strzałka B, Jankowiak R, Bilański P, Patel N, Hausner G, Linnakoski R, Solheim H (2020) Two new species of Ophiostomatales (Sordariomycetes) associated with the bark beetle Dryocoetes alni from Poland. MycoKeys 68: 23-48. https://doi.org/10.3897/mycokeys.68.50035

Figure 4 Phylogram obtained from Maximum Likelihood (ML) analyses of the combined datasets of ITS1-5.8S-ITS2-28S+ACT+TUB2+TEF1-α for selected species of Leptographiumsensu lato. Sequences obtained during this study are presented in bold type. The Bootstrap values ≥ 75% for ML and Maximum Parsimony (MP) analyses are presented at nodes as follows: ML/MP. Bold branches indicate posterior probabilities values ≥ 0.95 obtained from Bayesian Inference (BI) analyses. * Bootstrap values <75%. The tree is drawn to scale (see bar) with branch length measured in the number of substitutions per site. Leptographium flavum and L. vulnerum represents the outgroup in analyses of the combined datasets of ITS1-5.8S-ITS2-28S+ACT+TUB2+TEF1-α.

opencc-by-4.0Jun 2020View details →
zenodo28/100

Figure 1 from: Strzałka B, Jankowiak R, Bilański P, Patel N, Hausner G, Linnakoski R, Solheim H (2020) Two new species of Ophiostomatales (Sordariomycetes) associated with the bark beetle Dryocoetes alni from Poland. MycoKeys 68: 23-48. https://doi.org/10.3897/mycokeys.68.50035

Figure 1 Phylogram obtained from Maximum Likelihood (ML) analyses of the ITS1-5.8S-ITS2-28S data for the Ceratocystiopsis spp. Sequences obtained during this study are presented in bold type. The Bootstrap values ≥ 75% for ML and Maximum Parsimony (MP) analyses are presented at nodes as follows: ML/MP. Bold branches indicate posterior probabilities values ≥ 0.95 obtained from Bayesian Inference (BI) analyses. * Bootstrap values <75%. The tree is drawn to scale (see bar) with branch length measured in the number of substitutions per site. Ophiostoma karelicum and Ophiostoma quercus represent the outgroup.

opencc-by-4.0Jun 2020View details →
zenodo28/100

Figure 3 from: Strzałka B, Jankowiak R, Bilański P, Patel N, Hausner G, Linnakoski R, Solheim H (2020) Two new species of Ophiostomatales (Sordariomycetes) associated with the bark beetle Dryocoetes alni from Poland. MycoKeys 68: 23-48. https://doi.org/10.3897/mycokeys.68.50035

Figure 3 Phylogram obtained from Maximum Likelihood (ML) analyses of the ITS2-28S for selected species of Leptographiumsensu lato. Sequences obtained during this study are presented in bold type. The Bootstrap values ≥ 75% for ML and Maximum Parsimony (MP) analyses are presented at nodes as follows: ML/MP. Bold branches indicate posterior probabilities values ≥ 0.95 obtained from Bayesian Inference (BI) analyses. * Bootstrap values <75%. The tree is drawn to scale (see bar) with branch length measured in the number of substitutions per site. Ophiostoma karelicum and O. quercus represents the outgroup in analyses of ITS2-28S.

opencc-by-4.0Jun 2020View details →
zenodo28/100

Figure 2 from: Strzałka B, Jankowiak R, Bilański P, Patel N, Hausner G, Linnakoski R, Solheim H (2020) Two new species of Ophiostomatales (Sordariomycetes) associated with the bark beetle Dryocoetes alni from Poland. MycoKeys 68: 23-48. https://doi.org/10.3897/mycokeys.68.50035

Figure 2 Phylogram obtained from Maximum Likelihood (ML) analyses of TUB2 data for the Ceratocystiopsis spp. Sequences obtained during this study are presented in bold type. The Bootstrap values ≥ 75% for ML and Maximum Parsimony (MP) analyses are presented at nodes as follows: ML/MP. Bold branches indicate posterior probabilities values ≥ 0.95 obtained from Bayesian Inference (BI) analyses. * Bootstrap values <75%. The tree is drawn to scale (see bar) with branch length measured in the number of substitutions per site.

opencc-by-4.0Jun 2020View details →
zenodo28/100

Figure 2 from: Zheng H, Wan Y, Li J, Castañeda-Ruiz RF, Yu Z (2020) Phialolunulospora vermispora (Chaetosphaeriaceae, Sordariomycetes), a novel asexual genus and species from freshwater in southern China. MycoKeys 76: 17-30. https://doi.org/10.3897/mycokeys.76.57410

Figure 2 Phialolunulospora vermispora (YMF 1.04260) A colony on PDA at day 10 B conidia C–F conidiophores, conidiogenous cells and conidia G conidiogenous cells H, I conidiophores and conidiogenous cells. Scale bars: 10 mm (A); 10 μm (B–I).

opencc-by-4.0Dec 2020View details →
zenodo28/100

Figure 1 from: Zheng H, Wan Y, Li J, Castañeda-Ruiz RF, Yu Z (2020) Phialolunulospora vermispora (Chaetosphaeriaceae, Sordariomycetes), a novel asexual genus and species from freshwater in southern China. MycoKeys 76: 17-30. https://doi.org/10.3897/mycokeys.76.57410

Figure 1 Phylogenetic tree derived from Bayesian analysis based on ITS and LSU sequences, depicting the relationships of the new taxon Phialolunulospora vermispora with closely related taxa. The numbers above branches represent BIPP (left) and MLBPs (right). BIPP over 95% and MLBPs greater than 70% are shown on the respective branches, and the bar represents the substitutions per nucleotide position. Gelasinospora tetrasperma CBS 178.33, Sordaria fimicola CBS 508.50 and Lasiosphaeria ovina SMH 4605 were used as outgroup.

opencc-by-4.0Dec 2020View details →
dryad28/100

Data from: Correlated evolution of senescence and ephemeral substrate use in the Sordariomycetes

Evolutionary theory predicts that senescence – a decline in reproduction and survival with increasing age - can evolve as a trade-off between the investment in reproduction on one side and in somatic maintenance and repair on the other side. The ecology of a species is crucial here, since it provides the external causes of death that determine the statistical limit to a species' lifespan. Filamentous fungi are generally believed to be non-senescent, and there are indeed spectacular examples of very old fungal individuals in nature. Yet, for some fungi the growth conditions are ephemeral and therefore senescence is expected to have evolved, like in the coprophilic Podospora anserina, the only well-studied filamentous fungus with intrinsic senescence. Here we hypothesize that rapid senescence is more common in fungi than generally believed and that the phylogenetic distribution of senescence correlates with its ecology. We examined a set of Sordariomycetes for their lifespan and constructed phylogenies based on several nuclear sequences. Part of the strains were from the CBS culture collection, originally isolated from various substrates, some of which ephemeral. In addition we isolated new strains from short-lived substrates. Senescence was observed throughout the phylogeny. Correlation tests support the hypothesis that in the Sordariomycetes senescence is a trait that has arisen as an evolved adaptation to ephemeral substrates, and that it has evolved repeatedly and independently along the phylogeny.

opencc-zeroDec 2011View details →
zenodo28/100

Figure 4 from: Li L, Du H-Z, Thiyagaraja V, Bhat DJ, Phookamsak R, Cheewangkoon R (2024) Two novel freshwater hyphomycetes, in Acrogenospora (Minutisphaerales, Dothideomycetes) and Conioscypha (Conioscyphales, Sordariomycetes) from Southwestern China. MycoKeys 101: 249-273. https://doi.org/10.3897/mycokeys.101.115209

Figure 4 Conioscypha yunnanensis (KUN-HKAS 129616, holotype) a host specimen b colonies on submerged wood c conidiogenous cells bearing conidia (note: arrow points = cupulate conidionenous cells) d, e conidiogenous cell attached with conidia f–m conidia n germinated conidium o, p colony on PDA (o = up-front, p = down-reverse). Scale bars: 20 μm (c–n).

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure 3 from: Li L, Du H-Z, Thiyagaraja V, Bhat DJ, Phookamsak R, Cheewangkoon R (2024) Two novel freshwater hyphomycetes, in Acrogenospora (Minutisphaerales, Dothideomycetes) and Conioscypha (Conioscyphales, Sordariomycetes) from Southwestern China. MycoKeys 101: 249-273. https://doi.org/10.3897/mycokeys.101.115209

Figure 3 Acrogenospora alangii (KUN-HKAS 130312, holotype) a hostplant growing near water body b, c colonies on host substrate d–h conidiophores, conidiogenous cells and conidia i germinating conidium j, k colony on PDA (up-front, down-reverse) l, n conidia with apical appendages l–p conidia. Scale bars: 100 µm (d, e), 40 µm (f–i), 20 µm (l–p).

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure 2 from: Li L, Du H-Z, Thiyagaraja V, Bhat DJ, Phookamsak R, Cheewangkoon R (2024) Two novel freshwater hyphomycetes, in Acrogenospora (Minutisphaerales, Dothideomycetes) and Conioscypha (Conioscyphales, Sordariomycetes) from Southwestern China. MycoKeys 101: 249-273. https://doi.org/10.3897/mycokeys.101.115209

Figure 2 Phylogenetic tree constructed from RAxML analysis of LSU, ITS, SSU and RPB2 sequences data. Bootstrap support values for ML equal or greater than 50% and Bayesian posterior probabilities greater than 0.95 BPP are indicated at the nodes. The tree is rooted to Parafuscosporella moniliformis (MFLUCC 15–0626) and P. garethii (BCC79986). The new isolates are in red bold.

opencc-by-4.0Jan 2024View details →
zenodo28/100

Supplementary material 1 from: Li L, Du H-Z, Thiyagaraja V, Bhat DJ, Phookamsak R, Cheewangkoon R (2024) Two novel freshwater hyphomycetes, in Acrogenospora (Minutisphaerales, Dothideomycetes) and Conioscypha (Conioscyphales, Sordariomycetes) from Southwestern China. MycoKeys 101: 249-273. https://doi.org/10.3897/mycokeys.101.115209

Supplementary document

opencc-zeroJan 2024View details →
zenodo28/100

Figure 1 from: Li L, Du H-Z, Thiyagaraja V, Bhat DJ, Phookamsak R, Cheewangkoon R (2024) Two novel freshwater hyphomycetes, in Acrogenospora (Minutisphaerales, Dothideomycetes) and Conioscypha (Conioscyphales, Sordariomycetes) from Southwestern China. MycoKeys 101: 249-273. https://doi.org/10.3897/mycokeys.101.115209

Figure 1 Phylogenetic tree constructed from RAxML analysis of LSU, SSU, ITS, RPB2 and TEF1-α sequences data. Bootstrap support values for ML equal or greater than 50% and Bayesian posterior probabilities greater than 0.95 BPP are indicated at the nodes. The tree is rooted to Minutisphaera aspera (DSM29478) and Minutisphaera japonica (HHUF30098). The new isolates are in red bold.

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure 2 from: Chen X-M, Tang X, Ma J, Liu N-G, Tibpromma S, Karunarathna SC, Xiao Y-P, Lu Y-Z (2024) Identification of two new species and a new host record of Distoseptispora (Distoseptisporaceae, Distoseptisporales, Sordariomycetes) from terrestrial and freshwater habitats in Southern China. MycoKeys 102: 83-105. https://doi.org/10.3897/mycokeys.102.115452

Figure 2 Distoseptispora hainanensis (GZAAS 22-2047, holotype) a, b colonies on substrate c–e conidiophores and conidia f–h conidiogenous cells bearing conidia i, j conidiophores k–q conidia r, s colony on PDA (r from front s from reverse). Scale bars: 50 μm (c, d, f–j, l–q); 30 μm (e, k).

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 1 from: Chen X-M, Tang X, Ma J, Liu N-G, Tibpromma S, Karunarathna SC, Xiao Y-P, Lu Y-Z (2024) Identification of two new species and a new host record of Distoseptispora (Distoseptisporaceae, Distoseptisporales, Sordariomycetes) from terrestrial and freshwater habitats in Southern China. MycoKeys 102: 83-105. https://doi.org/10.3897/mycokeys.102.115452

Figure 1 Phylogenetic tree generated from ML analysis based on a combination of LSU, ITS, tef1-a, and rpb2 sequence data. Bootstrap support values of ML and MP equal to or greater than 75%, and PP value equal to or greater than 0.95 are given near the nodes as ML/PP/MP. The tree is rooted with Aquapteridospora aquatica (MFLUCC 17-2371). Ex-type strains are indicated by the superscript T. The new collections are in bold red text.

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 4 from: Chen X-M, Tang X, Ma J, Liu N-G, Tibpromma S, Karunarathna SC, Xiao Y-P, Lu Y-Z (2024) Identification of two new species and a new host record of Distoseptispora (Distoseptisporaceae, Distoseptisporales, Sordariomycetes) from terrestrial and freshwater habitats in Southern China. MycoKeys 102: 83-105. https://doi.org/10.3897/mycokeys.102.115452

Figure 4 Distoseptispora tectonae (GZAAS 22-2046) a, b colonies on substrate c, d conidiophores and conidia e, f conidiophores g–k conidia l germinated conidium m, n colonies on PDA (m from front n from reverse) Scale bars: 50 μm (c, d, g–l); 20 μm (e, f).

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 3 from: Chen X-M, Tang X, Ma J, Liu N-G, Tibpromma S, Karunarathna SC, Xiao Y-P, Lu Y-Z (2024) Identification of two new species and a new host record of Distoseptispora (Distoseptisporaceae, Distoseptisporales, Sordariomycetes) from terrestrial and freshwater habitats in Southern China. MycoKeys 102: 83-105. https://doi.org/10.3897/mycokeys.102.115452

Figure 3 Distoseptispora lanceolatispora (GZAAS 22-2045, holotype) a, b colonies on substrate c–e conidiophores and conidia f, g conidiogenous cells bearing conidia h–k conidia l germinated conidium m, n colony on PDA (m from front n from reverse). Scale bars: 50 μm (c–g); 30 μm (h–l).

opencc-by-4.0Feb 2024View details →

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