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64 results for “Botryosphaeriaceae”
FIGURE 7 in Resolving Tiarosporella spp. allied to Botryosphaeriaceae and Phacidiaceae
FIGURE 7. Sakireeta madreeya (CBS 532.76). A. Conidiomata on PNA. B–D. Conidiogenous cells. E, F. Conidia. Scale bars: A = 250 μm, all others = 10 μm.
FIGURE 5 in Resolving Tiarosporella spp. allied to Botryosphaeriaceae and Phacidiaceae
FIGURE 5. Darkera picea (CPC 23879). A. Conidiomata on OA. B–F. Conidiogenous cells. G–J. Conidia. Scale bars: A = 250 μm, all others = 10 μm.
FIGURE 1 in Resolving Tiarosporella spp. allied to Botryosphaeriaceae and Phacidiaceae
FIGURE 1. The first of 1000 equally most parsimonious trees (TL = 367; CI = 0.638; RI = 0.928; RC = 0.591) resulting from a parsimony analysis of the LSU (28S) sequence alignment. The bootstrap support values are indicated at the nodes (parsimony bootstrap / distance with HKY85 model bootstrap; only values>74%) and the scale bar represents the number of changes. Thickened branches reflect those branches present in the strict consensus tree. Orders are indicated in darker blue and orange blocks and family names
FIGURE 6 in Resolving Tiarosporella spp. allied to Botryosphaeriaceae and Phacidiaceae
FIGURE 6. Mucoharknessia cortaderiae (CPC 19974). A. Conidiomata on leaf blade of Cortaderia selloana. B. Aggregated conidiomata forming on PDA. C. Vertical section through a pycnidium, showing wall anatomy. D–G. Conidiogenous cells giving rise to conidia (note collarettes, F, G). H. Appendaged conidia with arrows indicating apical mucoid caps. I, J. Brown, finely verruculose, ellipsoid conidia. Scale bars: A, B = 300 μm, all others = 10 μm.
FIGURE 4 in Resolving Tiarosporella spp. allied to Botryosphaeriaceae and Phacidiaceae
FIGURE 4. Darkera parca (CPC 23904). A. Conidiomata on PNA. B. Conidiomata on OA. C–E. Conidiogenous cells. F–H. Conidia. Scale bars: A = 250 μm, all others = 10 μm.
FIGURE 3 in Resolving Tiarosporella spp. allied to Botryosphaeriaceae and Phacidiaceae
FIGURE 3. The single most parsimonious circle tree (TL = 22; CI = 1.0; RI = 1.0; RC = 1.0) resulting from an unrooted parsimony analysis of the combined ITS, LSU, SSU, TEF and TUB alignment strains of Darkera. Host countries are shown next to the culture accession number. The scale bar represents the number of changes.
FIGURE 2 in Resolving Tiarosporella spp. allied to Botryosphaeriaceae and Phacidiaceae
FIGURE 2. The first of 22 equally most parsimonious trees (TL = 619; CI = 0.577; RI = 0.809; RC = 0.467) resulting from a parsimony analysis of the combined ITS and LSU alignment representing genera in the Botryosphaeriaceae. The bootstrap support values are indicated at the nodes and the scale bar represents the number of changes. Thickened branches reflect those branches present in the strict consensus tree. Genus names in light blue and light brown blocks and abbreviated genus names used for the species follow from the genus name used for the corresponding clade. Species names of interest to this study are shown in bold text. The tree was rooted to Saccharata proteae (strain CBS 115206; ITS GenBank KF531812, LSU GenBank KF531812).
FIGURE 2 in Barriopsis tectonae sp. nov. a new species of Botryosphaeriaceae from Tectona grandis (teak) in Thailand
FIGURE 2. The most parsimonious trees (tree length= 1042, CI= 0.651, HI= 0.349, RI= 0.854, RC= 0.556) resulting from a combined ITS, TEF1-α and BT analysis for 38 taxa in the Botryosphaeriaceae. Maximum parsimony bootstrap values ≥70% are given above the nodes. Bayesian posterior probabilities ≥ 0.95 are given below the nodes. The tree was rooted to Pseudofusicoccum stromaticum.
FIGURE 1 in Barriopsis tectonae sp. nov. a new species of Botryosphaeriaceae from Tectona grandis (teak) in Thailand
FIGURE 1. Barriopsis tectonae (MFLU 14-0024, holotype) A. Ascostromata on host. B. Ascostromata cut through horizontally showing the white contents with dark spots. C–D. Section through ascoma on host. E. Papilla with periphyses. F. Peridium. G. Pseudoparaphyses. H. Immature ascus. I–J. Immature ascus with hyaline ascospores, mature asci with brown ascospores. K, M. Mature ascospore/s without terminal apiculi. L. Immature ascopsore without longitudinal striations. N. Germinated ascospore. O. Immature conidium. P. Mature conidium with two septa. Q, R. Mature conidia with longitudinal striations. Scale bars: A, B = 500 µm, C = 100 µm, D, K = 50 µm, E, H–J, N = 20 µm, F, G, L, M, O–R = 10 µm.
FIGURE 2 in Diplodia parva sp. nov., a novel species of the family Botryosphaeriaceae isolated from soil in Korea
FIGURE 2. Cultural and morphological characteristics of Diplodia parva KNU16-007. A, B and C, pycnidia on pine needle; D, conidiophore; E, front and reverse view of the colony on PDA; F, front and reverse view of the colony on MEA; G, conidiogenous cells; H, conidia. Scale bars: A, B = 100 µm; C, D, G, H = 10 µm.
FIGURE 3 in Diplodia parva sp. nov., a novel species of the family Botryosphaeriaceae isolated from soil in Korea
FIGURE 3. Neighbor-joining phylogenetic tree based on the concatenated ITS and TEF1-α sequences showing the phylogenetic position of Diplodia parva KNU16-007 among the Diplodia species. Bootstrap values (based on 1000 replications) greater than 60% are shown at branch points. Filled circles indicate that the corresponding nodes were also recovered in trees generated using the maximum-likelihood and maximum-parsimony algorithms. Open circles indicate that the corresponding nodes were also recovered in the tree generated using the maximum-likelihood or maximum-parsimony algorithm. The isolated strain is shown in bold. Lasiodiplodia theobromae CBS 164.96 was used as an outgroup. Bar, 0.01 substitutions per nucleotide position.
FIGURE 3 in Additions to Karst Fungi 5: Sardiniella guizhouensis sp. nov. (Botryosphaeriaceae) associated with woody hosts in Guizhou province, China
FIGURE 3. Sardiniella guizhouensis (GZAAS 19-1935, sexual morph) a, b. Appearance of ascostromata on decaying aerial stem. c. Peridium. d. Vertical section of ascostromata. e. Mature and immature asci. f. Immature ascus. g–i. Mature asci. j–l. Mature brown 1-celled ascospores. m, n. Mature brown 1-septate ascospores. o. 5d old culture on PDA from above. p. 5d old culture on PDA from reverse. Scale bars: c=50μm, d=100μm, e=20μm, f–n=10μm.
FIGURE 1 in Additions to Karst Fungi 5: Sardiniella guizhouensis sp. nov. (Botryosphaeriaceae) associated with woody hosts in Guizhou province, China
FIGURE 1. Maximum likelihood (ML) majority rule consensus tree for the analyzed Botryosphaeriaceae genera based on combined LSU, ITS and tef1 sequence data. RAxML bootstrap support values (ML) and maximum parsimony (MP) are given at the nodes (ML/MP). Branches are in bold indicate Bayesian posterior probabilities> 0.95. Isolate numbers of ex-types and reference strains are in bold. Species isolated in this study are in ted. The tree was rooted to Melanops tulasnei (CBS 116805).
FIGURE 2 in Additions to Karst Fungi 5: Sardiniella guizhouensis sp. nov. (Botryosphaeriaceae) associated with woody hosts in Guizhou province, China
FIGURE 2. Sardiniella guizhouensis (HKAS 113023, holotype). a, b. Conidiomata on host surface. c, d. Vertical section of multiloculate conidiomata. e–h. Conidiogenous cells and developing conidia. i–l. Immature, hyaline conidia. m, n. Mature, brown 1-septate conidia. Scale bars: c=50 μm, d=10 μm, e=50 μm, f=20 μm, g–n=10 μm.
FIGURE 2 in Morpho-phylogenetic evidence reveals Lasiodiplodia chiangraiensis sp. nov. (Botryosphaeriaceae) associated with woody hosts in northern Thailand
FIGURE 2. Lasiodiplodia chiangraiensis (MFLU 21-0003, holotype). a–c. Conidiomata on host surface. d. Section through conidiomata. e. Peridium. f. Ostiolar region with periphyses. g. Paraphyses. h–k. Conidia developing on conidiogenous cells. l–o. Hyaline, aseptate conidia. p. Germinating conidium. q, r. Colonies after 7 days on PDA (q from above, r from below). Scale bars: b = 500 μm, c = 200 μm, d–e = 10 μm, f = 20 μm, g–p = 10 μm.
FIGURE 1 in Morpho-phylogenetic evidence reveals Lasiodiplodia chiangraiensis sp. nov. (Botryosphaeriaceae) associated with woody hosts in northern Thailand
FIGURE 1. Phylogenetic tree generated from maximum parsimony (MP) analysis based on combined ITS, tef and tub2 sequence data of Lasiodiplodia. Bootstrap values for maximum likelihood (ML) and maximum parsimony (MP) equal to or greater than 75% are placed above and below the branches, respectively. Branches with Bayesian posterior probabilities (BYPP) equal or greater than 0.95 are thickened. The new isolates are indicated in red and ex-type strains are in bold. The tree is rooted to Diplodia mutila (CMW 7060) and D. seriata (CBS 112555). The scale bar shows 20 changes.
FIGURE 2 in Neodeightonia septata sp. nov. and N. subglobosa (Botryosphaeriaceae) from northern Thailand
FIGURE 2. Neodeightonia septata (MFLU 22-0003, holotype). a. Substrate with conidiomata. b, c. Appearance of black conidiomata on palm culm. d. Vertical section of conidiomata. e. Section of peridium. f. Ostiolar region. g–i. Conidiogenous cells and developing conidia. j–m. Hyaline, aseptate immature conidia. n. Brown, 1-septate mature conidia. o. Germinating conidium. p, q. Colonies after 7 days on PDA (p from above, q from below). Scale bars: b = 50 μm, c = 10 μm, d–f = 20 μm, g–o = 5 μm.
FIGURE 1 in Neodeightonia septata sp. nov. and N. subglobosa (Botryosphaeriaceae) from northern Thailand
FIGURE 1. Phylogenetic tree generated from maximum likelihood (ML) analysis based on combined ITS, LSU, SSU and tef sequence data for all accepted species of Neodeightonia and closely related genera within the family Botryosphaeriaceae. Bootstrap values for maximum likelihood (ML) and maximum parsimony (MP) equal to or greater than 75% are placed above and below the branches, respectively. Bayesian posterior probabilities (BYPP) equal or greater than 0.95 are denoted in thickened branches. The strain numbers are given after the species names, and ex-type strains are indicated in bold. The newly generated isolates are in red. The tree is rooted with two isolates of Barriopsis iraniana (IRAN 1448C, IRAN 1451C).
FIGURE 2. Phylogram generated from maximum likelihood analysis resulting from the combined ITS, tef1 and tub2 in Interesting Botryosphaeria (Botryosphaeriaceae) associated with Magnolia species in Thailand: Additions of two new host records with their lifestyles
FIGURE 2. Phylogram generated from maximum likelihood analysis resulting from the combined ITS, tef1 and tub2 sequence dataset. Related sequences of Botryosphaeria were obtained from Zhang et al. (2021). Cophinforma eucalypti (MFLUCC 11-0425) was selected as the outgroup taxon. Bootstrap values for maximum likelihood equal to or greater than 60% and bayesian posterior probabilities equal to or greater than 0.95 are placed above the branches. The newly generated sequences are indicated in red. Type and ex-type strains are in black bold. Species names and strain accession numbers are followed by the lifestyle (orange), the isolation source or host species (green) and country of origin (blue). The accepted species names (according to Zhang et al. 2021) are indicated to the left of each clade. The scale bar represents the expected number of changes per site. The tree was rooted to Cophinforma eucalypti (MFLUCC 11-0425). END: Endophytic; PAT: Pathogenic; SAP: Saprobic; UNK: Unknown.
FIGURE 3 in Interesting Botryosphaeria (Botryosphaeriaceae) associated with Magnolia species in Thailand: Additions of two new host records with their lifestyles
FIGURE 3. Botryosphaeria puerensis (HKAS 107129, new host record). a–c. Appearance of ascomata on substrate. d, e. Sections through ascomata. f. Peridium. g. Paraphyses. h–j. Asci. k–n. Ascospores. Scale bars: a, b = 500 μm, c = 200 μm, d, e = 50 μm, f, h–j = 20 μm, g = 10 μm, k–n = 5 μm.
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