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41 results for “Didymosphaeriaceae”
Figure 3 from: Samarakoon BC, Wanasinghe DN, Samarakoon MC, Phookamsak R, McKenzie EH.C, Chomnunti P, Hyde KD, Lumyong S, Karunarathna SC (2020) Multi-gene phylogenetic evidence suggests Dictyoarthrinium belongs in Didymosphaeriaceae (Pleosporales, Dothideomycetes) and Dictyoarthrinium musae sp. nov. on Musa from Thailand. MycoKeys 71: 101-118. https://doi.org/10.3897/mycokeys.71.55493
Figure 3 Dictyoarthrinium sacchari (MFLU 20-0439) a conidia on the host b developmental stage of terminal conidium attached to the conidiophore c–f Conidiophores and conidia (e, with distinct mother cell) g, h mature conidiophores with four-celled terminal conidium i conidiophore with two celled terminal conidium j developmental stages of conidia on conidiophore k colony on PDA after 21 days l–q conidia. Scale bars: a = 1000 μm (a); 20 μm (b, j); 50 μm (c–i); 5 μm (l–q).
Figure 2 from: Samarakoon BC, Wanasinghe DN, Samarakoon MC, Phookamsak R, McKenzie EH.C, Chomnunti P, Hyde KD, Lumyong S, Karunarathna SC (2020) Multi-gene phylogenetic evidence suggests Dictyoarthrinium belongs in Didymosphaeriaceae (Pleosporales, Dothideomycetes) and Dictyoarthrinium musae sp. nov. on Musa from Thailand. MycoKeys 71: 101-118. https://doi.org/10.3897/mycokeys.71.55493
Figure 2 Dictyoarthrinium musae (MFLU 20-0437, holotype) a conidia on the host b conidiophore and conidia with conidiophore mother cell c–f conidia with conidiophores on stalk g developmental stage of an immature lateral conidium h four-celled terminal conidium i conidiophore j conidiophores and conidia with terminal conidium k, l conidiophores without terminal conidium m attachment of a mature lateral conidium n–q warted four-celled mature conidia r, s mature conidia that split at septa t colony on PDA after 21 days. Scale bars: 500 μm (a); 50 μm (b, c); 20 μm (d–g, i); 10 μm (h); 5 μm (j–s).
Figure 1 from: Samarakoon BC, Wanasinghe DN, Samarakoon MC, Phookamsak R, McKenzie EH.C, Chomnunti P, Hyde KD, Lumyong S, Karunarathna SC (2020) Multi-gene phylogenetic evidence suggests Dictyoarthrinium belongs in Didymosphaeriaceae (Pleosporales, Dothideomycetes) and Dictyoarthrinium musae sp. nov. on Musa from Thailand. MycoKeys 71: 101-118. https://doi.org/10.3897/mycokeys.71.55493
Figure 1 Maximum Likelihood tree revealed by RAxML from an analysis of SSU, LSU and ITS and tef1-α sequence data of the genera of Didymosphaeriaceae, showing the phylogenetic position of Dictyoarthrinium musae (MFLUCC 20-0105, MFLUCC 20-0106) and D. sacchari (MFLUCC 20-0107). ML bootstrap supports (≥ 60%) and Bayesian posterior probabilities (≥ 0.95 BYPP) are given above the branches, respectively. The tree is rooted with Bambusistroma didymosporum (MFLU 15-0057 and MFLU 15-0058). Strains generated in this study are indicated in brown bold type. Ex-type strains are indicated in black bold. The scale bar represents the expected number of nucleotide substitutions per site.
Figure 4 from: Samarakoon BC, Wanasinghe DN, Samarakoon MC, Phookamsak R, McKenzie EH.C, Chomnunti P, Hyde KD, Lumyong S, Karunarathna SC (2020) Multi-gene phylogenetic evidence suggests Dictyoarthrinium belongs in Didymosphaeriaceae (Pleosporales, Dothideomycetes) and Dictyoarthrinium musae sp. nov. on Musa from Thailand. MycoKeys 71: 101-118. https://doi.org/10.3897/mycokeys.71.55493
Figure 4 Morphology of conidia and conidiophores of previously described Dictyoarthrinium species a, dD. microsporumb, iD. synnematicumc, eD. lilliputeumf, jD. africanumg, h, kD. rabaulense. Scale bars: 20 μm (a, c, d, e); 10 μm (b, i). Magnification × 650 (f, g, h, j, k). Redrawn from Rao and Rao (1964), Ellis (1971), Kobayasi et al. (1971) and Somrithipol (2007).
Figure 6 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259
Figure 6 Montagnula lijiangensis (HKAS 126541, holotype) a, b ascomata on natural wood surface c vertical section through an ascoma d ostiolar neck and peridium cells at the apex e pseudoparaphyses f–i asci j–o ascospores (see verruculose feature of the ascospore in k). Scale bars: 100 μm (c); 20 μm (d, f–i); 10 μm (e–o).
Figure 9 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259
Figure 9 Montagnula thevetiae (HKAS 126564, holotype). a, b ascomata on natural wood surface c vertical section through an ascoma d closeup of ostiole e pseudoparaphyses f–h asci j–l ascospores m, n culture characteristics on PDA (m = above, n = reverse). Scale bars: 100 μm (c); 50 μm (d, f–h); 10 μm (e, i–l).
Figure 5 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259
Figure 5 Montagnula aquilariae (HKAS 126542) a, b ascomata on natural wood surface c vertical section through an ascoma d ostiolar neck e peridium cells at the apex f peridium cells at the side g pseudoparaphyses h–l asci m–r ascospores (see verruculose feature of the ascospore in r) s, t culture characters on PDA (s = above, t = reverse). Scale bars: 100 μm (c, d); 50 μm (e); 10 μm (e–g, m–r); 20 μm (h–l).
Figure 2 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259
Figure 2 Geographical distribution of Montagnula species with known ITS sequence data. a the map summarizes data from the GlobalFungi database (shown by circles). Each circle symbolizes a unique sample, with each color representing the specific biome from which it has been collected b the distribution of Montagnula sequences as a percentage of total abundance across different biomes c the distribution of Montagnula sequences as a percentage of total abundance across different continents. See Suppl. material 1 for primary data.
Figure 4 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259
Figure 4 The species richness of recorded Montagnula species across different plant families (Table 1).
Figure 3 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259
Figure 3 The distribution of Montagnula occurrences across oceans, continents and various substrates, as documented in the existing literature. On the x-axis, the logarithmic abundance of each record for different sources is displayed.
Figure 1 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259
Figure 1 Phylogenetic analysis of SSU, LSU, ITS, tef1-α, and rpb2 of the Montagnula. Species names given in bold are ex-type, ex-epitype and ex-paratype strains. Species names highlighted in blue are generated from this study. Branch support of nodes ≥75% ML BS and ≥0.95 PP is indicated above the branches. The genus Montagnula is depicted within a pale gray box, with new species highlighted in white, and the outgroup indicated by a blue box.
Figure 8 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259
Figure 8 Montagnula shangrilana (HKAS 126541, holotype) a ascomata on natural wood surface b vertical section through an ascoma c pseudoparaphyses d peridium cells e–h asci i–o ascospores (see verruculose feature of the ascospore in o). Scale bars: 100 μm (b); 10 μm (c, d, j–o); 20 μm (e–h).
Figure 7 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259
Figure 7 Montagnula menglaensis (HKAS 130318, holotype) a–c ascomata on natural wood surface d, e vertical section through ascomata f, g pseudoparaphyses h peridium i–k asci l, m ascospores (see verruculose feature of the ascospore in n) o, p culture characters on PDA (o = above, p = reverse) q, r conidiomata s pycnidial wall t conidia. Scale bars: 100 μm (d, e); 10 μm (f–h, l–n, s, t); 20 μm (i–k).
FIGURE 3 in Molecular phylogeny and diversity of Laburnicola (Didymosphaeriaceae): a new species from Uzbekistan
FIGURE 3. Distribution map of Laburnicola species
Figure 3 from: Gonçalves MFM, Vicente TFL, Esteves AC, Alves A (2019) Neptunomyces aureus gen. et sp. nov. (Didymosphaeriaceae, Pleosporales) isolated from algae in Ria de Aveiro, Portugal. MycoKeys 60: 31-44. https://doi.org/10.3897/mycokeys.60.37931
Figure 3 Phylogenetic relationships of Didymosphaeriaceae species based on ITS and tef1-α sequence data and inferred using the Maximum Likelihood method under the Kimura 2-parameter model. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site and rooted to Cucurbitaria berberidis (CBS 130007) and Coniothyrium palmarum (CBS 400.71). Bootstrap values (> 70%) are shown at the nodes. Ex-type strains are in bold and the isolates from the current study are in blue.
Supplementary material 1 from: Gonçalves MFM, Vicente TFL, Esteves AC, Alves A (2019) Neptunomyces aureus gen. et sp. nov. (Didymosphaeriaceae, Pleosporales) isolated from algae in Ria de Aveiro, Portugal. MycoKeys 60: 31-44. https://doi.org/10.3897/mycokeys.60.37931
: Data type: species data
Figure 4 from: Gonçalves MFM, Vicente TFL, Esteves AC, Alves A (2019) Neptunomyces aureus gen. et sp. nov. (Didymosphaeriaceae, Pleosporales) isolated from algae in Ria de Aveiro, Portugal. MycoKeys 60: 31-44. https://doi.org/10.3897/mycokeys.60.37931
Figure 4 Neptunomyces aureus (MUM 19.38). A, B Colony after 2 weeks at 25 °C on PDA (obverse and reverse) C, D colony after 2 weeks at 25 °C on MEA (obverse and reverse) E, F colony after 2 weeks at 25 °C on OA (obverse and reverse) G, H conidiomata after 1 month at 25 °C on pine needles and PDA. I, J conidiogenous cells K conidia. Scale bars: 2.5 μm.
Figure 2 from: Gonçalves MFM, Vicente TFL, Esteves AC, Alves A (2019) Neptunomyces aureus gen. et sp. nov. (Didymosphaeriaceae, Pleosporales) isolated from algae in Ria de Aveiro, Portugal. MycoKeys 60: 31-44. https://doi.org/10.3897/mycokeys.60.37931
Figure 2 Phylogenetic relationships of Didymosphaeriaceae species based on ITS and tub2 sequence data and inferred using the Maximum Likelihood method under the Kimura 2-parameter model. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site and rooted to Cucurbitaria berberidis (CBS 130007) and Coniothyrium palmarum (CBS 400.71). Bootstrap values (> 70%) are shown at the nodes. Ex-type strains are in bold and the isolates from the current study are in blue.
Figure 1 from: Gonçalves MFM, Vicente TFL, Esteves AC, Alves A (2019) Neptunomyces aureus gen. et sp. nov. (Didymosphaeriaceae, Pleosporales) isolated from algae in Ria de Aveiro, Portugal. MycoKeys 60: 31-44. https://doi.org/10.3897/mycokeys.60.37931
Figure 1 Phylogenetic relationships of Didymosphaeriaceae species based on ITS sequence data and inferred using the Maximum Likelihood method under the Kimura 2-parameter model. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site and rooted to Cucurbitaria berberidis (CBS 130007) and Coniothyrium palmarum (CBS 400.71). Bootstrap values (> 70%) are shown at the nodes. Ex-type strains are in bold and the isolates from the current study are in blue.
FIGURE 1 in Molecular phylogeny and diversity of Laburnicola (Didymosphaeriaceae): a new species from Uzbekistan
FIGURE 1. Phylogram generated from maximum likelihood analysis based on combined LSU, SSU, ITS and TEF 1-ɑ sequence data. Periconia citlatepetlensis strains (IOM 325319, IOM 325319.2) are used as the outgroup. Bootstrap support values for ML equal to or greater than 60% and BYPP equal to or greater than 0.95 are given above the branches. The ex-type strains are in bold and black; the new isolate is in bold and red.
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