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37 results for “Amphisphaeriales”
Supplementary material 2 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Phylogenetic trees generated by maximum parsimony analysis of single and combined ITS, tub2 and tef1-α sequence data
FIGURE 2 in An appendage-bearing coelomycete Pseudotruncatella arezzoensis gen. and sp. nov. (Amphisphaeriales genera incertae sedis) from Italy, with notes on Monochaetinula
FIGURE 2. Pseudotruncatella arezzoensis (MFLU 15-2285, holotype) a, b. Conidiomata on host substrate. c. Vertical section of conidioma. d. Section through peridium. e–g. Conidiogenous cells. with mature and immature conidia. h–k. Mature conidia. k. Germinating conidium. m, n. Cultures on PDA. Scale bars: b = 500 μm, c = 100 μm, d–k = 20 μm.
FIGURE 1 in An appendage-bearing coelomycete Pseudotruncatella arezzoensis gen. and sp. nov. (Amphisphaeriales genera incertae sedis) from Italy, with notes on Monochaetinula
FIGURE 1. The ML consensus tree inferred from the combined LSU, SSU and ITS sequence data of selected taxa of Xylariomycetidae. Values above or below the branches indicate maximum likelihood and maximum parsimony bootstrap ≥ 50%, (ML/MP). Values at the third position, respectively, above or below the branches represent posterior probabilities (PP ≥ 0.95). The ex-types strains are in bold, the new isolates are in blue. The tree is rooted to Diaporthe rudis, Dinemasporium nelloi and Trichoderma viride.
Supplementary material 1 from: Liu R, Li D, Zhang Z, Liu S, Liu X, Wang Y, Zhao H, Liu X, Zhang X, Xia J, Wang Y (2023) Morphological and phylogenetic analyses reveal two new species and a new record of Apiospora (Amphisphaeriales, Apiosporaceae) in China. MycoKeys 95: 27-45. https://doi.org/10.3897/mycokeys.95.96400
Morphological and phylogenetic analyses reveal two new species and a new record of Apiospora (Amphisphaeriales, Apiosporaceae) in China
Supplementary material 1 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
The morphological features of Pestalotiopsissensu lato fungi and GenBank accession numbers
Figure 8 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 8 Neopestalotiopsis camelliae-oleiferae (NTUPPMCC 18-166 = CD08) A the original habitat of Neopestalotiopsis camelliae-oleiferae; the stroma of Tolypocladium sp. hyperparasitic on an ascocarps of Elaphomyces sp. (Ascomycota) B top view (left) and bottom view (right) of the colony on potato dextrose agar (PDA) after incubation for seven days C conidiomata on carnation leaf D, E conidiogenous cells and immature conidia F–I conidia. Scale bars: 250 μm (C); 20 μm (D–I).
Figure 7 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 7 Split graphs showing the results of PHI tests for three gene regions (AITSBtub2Ctef1-α) of Pestalotiopsis manyueyuanani with their phylogenetically closely -related species using LogDet transformation and splits decomposition options. The new taxon in each graph is shown in red and taxa representing ex-type strains are in bold.
Figure 5 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 5 Pestalotiopsis hispanica (NTUPPMCC 18-162 = CD03) A the original habitat of Pestalotiopsis hispanica; the stroma of Ophiocordyceps sp. B top view (left) and bottom view (right) of the colony on potato dextrose agar (PDA) after incubation for seven days C conidiomata on carnation leaf D, E conidiogenous cells and immature conidia F–I conidia. Scale bars: 250 μm (C); 10 μm (D–I).
Figure 4 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 4 Pestalotiopsis chamaeropis (NTUPPMCC 21-054 = CD09) A the original habitat of Pestalotiopsis chamaeropis; the stroma of Ophiocordyceps sp. B top view (left) and bottom view (right) of the colony on potato dextrose agar (PDA) after incubation for seven days C conidiomata on carnation leaf D, E conidiogenous cells and immature conidia F–I conidia. Scale bars: 250 μm (C); 20 μm (D–I).
Figure 10 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 10 Conidial morphology of Pestalotiopsis formosana (A, B NTUPPMCC 21-056), Pestalotiopsis trachycarpicola (C NTUPPMCC 18-160 D NTUPPMCC 21-055) and Neopestalotiopsis sp. (E NTUPPMCC 18-161), isolated from entomopathogenic fungi in this study. Scale bars: 20 μm (A–E).
Figure 3 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 3 ML Phylogenetic tree of genus Neopestalotiopsis attained from the concatenated DNA sequence data of ITS, tub2 and tef1-α loci implemented via IQ-TREE. ML bootstrap values (MLB) ≥ 70%, Maximum Parsimony bootstrap (MPB) values ≥ 70% and Bayesian Posterior Probabilities (PP) ≥ 0.95 are given at the nodes. The scale-bar shows the number of estimated substitutions per site. Pseudopestalotiopsis theae (MFLUCC 12-0055) was used as an outgroup. The new isolates are in red and taxa representing ex-type cultures are in bold.
Figure 12 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 12 Comparison of the mycelium growth rates of eight pestalotiopsis-like fungal strains at 25 °C. According to Tukey's range test, data (mean ± standard deviation) with the same letters are not significantly different. Colours represent different taxa: NTUPPMCC 18-160, Pestalotiopsis trachycarpicola; NTUPPMCC 18-161, Neopestalotiopsis sp.; NTUPPMCC 18-162, Pestalotiopsis hispanica; NTUPPMCC 18-163, Neopestalotiopsis haikouensis; NTUPPMCC 18-165, Pestalotiopsis manyueyuanani.; NTUPPMCC 18-166, Neopestalotiopsis camelliae-oleiferae; NTUPPMCC 21-054, Pestalotiopsis chamaeropis; NTUPPMCC 21-056, Pestalotiopsis formosana.
Figure 13 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 13 Optimal pH for mycelial growth of each species according to the comparison of colonial growth (mm) of different species at each pH, based on the mean values presented in Table S12. Colours represent different taxa: NTUPPMCC 18-160, Pestalotiopsis trachycarpicola; NTUPPMCC 18-161, Neopestalotiopsis sp.; NTUPPMCC 18-162, Pestalotiopsis hispanica; NTUPPMCC 18-163, Neopestalotiopsis haikouensis; NTUPPMCC 18-165, Pestalotiopsis manyueyuanani.; NTUPPMCC 18-166, Neopestalotiopsis camelliae-oleiferae; NTUPPMCC 21-054, Pestalotiopsis chamaeropis; NTUPPMCC 21-056, Pestalotiopsis formosana.
Figure 2 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 2 ML phylogenetic tree of Pestalotiopsis obtained from the concatenated DNA sequence data of ITS, tub2 and tef1-α genes implemented in IQ-TREE. ML bootstrap values (MLB) ≥ 70%, Maximum Parsimony bootstrap (MPB) values ≥ 70% and Bayesian Posterior Probabilities (PP) ≥ 0.95 are given at the nodes. The scale-bar shows the number of estimated substitutions per site. Neopestalotiopsis protearum (CBS 114178) was used as an outgroup. The new isolates are in red and taxa representing ex-type cultures are in bold.
Figure 1 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 1 The habitat of Pestalotiopsis and Neopestalotiopsis species, situated on the stromata of entomopathogenic fungi. Specimens AOphiocordyceps sp. NTUPPMH 18-160 BBeauveria sp. NTUPPMH 18-161 CTolypocladium sp. NTUPPMH 21-055 DOphiocordyceps sp. NTUPPMH 21-054 EOphiocordyceps sp. NTUPPMH 21-053 FOphiocordyceps sp. NTUPPMH 18-164 G, H the section of conidioma of Ophiocordyceps sp. showing the location of conidia of pestalotiopsis-like fungi (red arrow). Scale bars: 100 μm (G); 20 μm (H).
Figure 6 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 6 The morphology of Pestalotiopsis manyueyuananiA the original habitat of conidia of Pestalotiopsis manyueyuanani; stroma of Ophiocordyceps sp. B top view (left) and bottom view (right) of the colony on potato dextrose agar (PDA) after incubation for seven days C formation of conidiomata on carnation leaf D, E conidiogenous cells and immature conidia F–K conidia L–N germinated conidia. Scale bars: 250 μm (C); 10 μm (D–K); 20 μm (L–N).
Figure 9 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 9 Neopestalotiopsis haikouensis (NTUPPMCC 18-163 = CD04) A the original habitat of Neopestalotiopsis haikouensis; the stroma of Ophiocordyceps sp. B top view (left) and bottom view (right) of the colony on potato dextrose agar (PDA) after incubation for seven days C conidiomata on carnation leaf D, E conidiogenous cells and immature conidia F–I conidia. Scale bars: 250 μm (C); 20 μm (D–I).
Figure 11 from: Hsu S-Y, Xu Y-C, Lin Y-C, Chuang W-Y, Lin S-R, Stadler M, Tangthirasunun N, Cheewangkoon R, AL-Shwaiman HA, Elgorban AM, Ariyawansa HA (2024) Hidden diversity of Pestalotiopsis and Neopestalotiopsis (Amphisphaeriales, Sporocadaceae) species allied with the stromata of entomopathogenic fungi in Taiwan. MycoKeys 101: 275-312. https://doi.org/10.3897/mycokeys.101.113090
Figure 11 Temperature effect on mycelial growth according to the comparison of colonial growth (mm) of different species at each temperature, based on the mean values presented in Table S11. Colours represent different taxa: NTUPPMCC 18-160, Pestalotiopsis trachycarpicola; NTUPPMCC 18-161, Neopestalotiopsis sp.; NTUPPMCC 18-162, Pestalotiopsis hispanica; NTUPPMCC 18-163, Neopestalotiopsis haikouensis; NTUPPMCC 18-165, Pestalotiopsis manyueyuanani.; NTUPPMCC 18-166, Neopestalotiopsis camelliae-oleiferae; NTUPPMCC 21-054, Pestalotiopsis chamaeropis; NTUPPMCC 21-056, Pestalotiopsis formosana.
Supplementary material 6 from: Wang Y, Tsui K-M, Chen S, You C (2024) Diversity, pathogenicity and two new species of pestalotioid fungi (Amphisphaeriales) associated with Chinese Yew in Guangxi, China. MycoKeys 102: 201-224. https://doi.org/10.3897/mycokeys.102.113696
Nucleotide differences between the isolates in this study
Supplementary material 5 from: Wang Y, Tsui K-M, Chen S, You C (2024) Diversity, pathogenicity and two new species of pestalotioid fungi (Amphisphaeriales) associated with Chinese Yew in Guangxi, China. MycoKeys 102: 201-224. https://doi.org/10.3897/mycokeys.102.113696
Effects of carbon sources on growth of isolates
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