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zenodo28/100

Figure 4 from: Yang Q, Tang J, Zhou GY (2021) Characterization of Diaporthe species on Camellia oleifera in Hunan Province, with descriptions of two new species. MycoKeys 84: 15-33. https://doi.org/10.3897/mycokeys.84.71701

Figure 4 Diaporthe hunanensis (HNZZ023) A Culture on PDAB conidiomata C conidiogenous cells D alpha conidia. Scale bars: 500 μm (B); 10 μm (C–D).

opencc-by-4.0Oct 2021View details →
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Figure 3 from: Yang Q, Tang J, Zhou GY (2021) Characterization of Diaporthe species on Camellia oleifera in Hunan Province, with descriptions of two new species. MycoKeys 84: 15-33. https://doi.org/10.3897/mycokeys.84.71701

Figure 3 Diaporthe hubeiensis (HNZZ019) A Culture on PDAB conidiomata C conidiogenous cells D alpha conidia. Scale bars: 500 μm (B); 10 μm (C–D).

opencc-by-4.0Oct 2021View details →
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Figure 2 from: Yang Q, Tang J, Zhou GY (2021) Characterization of Diaporthe species on Camellia oleifera in Hunan Province, with descriptions of two new species. MycoKeys 84: 15-33. https://doi.org/10.3897/mycokeys.84.71701

Figure 2 Diaporthe camelliae-oleiferae (HNZZ027) A Culture on PDAB conidiomata C conidiogenous cells D–F alpha and beta conidia. Scale bars: 200 μm (B); 10 μm (C–D); 20 μm (E, F).

opencc-by-4.0Oct 2021View details →
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Figure 3 from: Hurdeal VG, Gentekaki E, Hyde KD, Nguyen TTT, Lee HB (2021) Novel Mucor species (Mucoromycetes, Mucoraceae) from northern Thailand. MycoKeys 84: 57-78. https://doi.org/10.3897/mycokeys.84.71530

Figure 3 Mucor chiangraiensis (MFLU 21–0079) a–e columella with and without collars f, g sporangia h–i chlamydospores j sporangiospores k front and reverse of the colony grown in MEA. Scale bars: 10 µm (a–j).

opencc-by-4.0Oct 2021View details →
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Figure 2 from: Hurdeal VG, Gentekaki E, Hyde KD, Nguyen TTT, Lee HB (2021) Novel Mucor species (Mucoromycetes, Mucoraceae) from northern Thailand. MycoKeys 84: 57-78. https://doi.org/10.3897/mycokeys.84.71530

Figure 2 Mucor aseptatophorus (MFLU 21–0145) a–c columella with collar d branching of sporangiophores e, f developing sporangium g short sporangiophore with sporangium h rhizoids i granular content in mycelium j sporangiospores k front and reverse of the colony in MEA. Scale bars: 10 µm (a–c, e–h, j); 20 µm (d, i).

opencc-by-4.0Oct 2021View details →
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Figure 4 from: Hurdeal VG, Gentekaki E, Hyde KD, Nguyen TTT, Lee HB (2021) Novel Mucor species (Mucoromycetes, Mucoraceae) from northern Thailand. MycoKeys 84: 57-78. https://doi.org/10.3897/mycokeys.84.71530

Figure 4 Mucor nederlandicus (MFLU 21–007) a-c columella with highly reduced collar d sterile sporangium e columella with visible collar f-h chlamydospores i mature sporangia j sporangiospores k front and reverse of the colony in MEA. Scale bars: 20 µm (a–e, i); 10 µm (f–h).

opencc-by-4.0Oct 2021View details →
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Figure 84 from: Bruneau A, Queiroz LP, Ringelberg JJ, Borges LM, Bortoluzzi RLC, Brown GK, Cardoso DBOS, Clark RP, Conceição AS, Cota MMT, Demeulenaere E, Duno de Stefano R, Ebinger JE, Ferm J, Fonseca-Cortés A, Gagnon E, Grether R, Guerra E, Haston E, Herendeen PS, Hernández HM, Hopkins HCF, Huamantupa-Chuquimaco I, Hughes CE, Ickert-Bond SM, Iganci J, Koenen EJM, Lewis GP, Lima HC, Lima AG, Luckow M, Marazzi B, Maslin BR, Morales M, Morim MP, Murphy DJ, O'Donnell SA, Oliveira FG, Oliveira ACS, Rando JG, Ribeiro PG, Ribeiro CL, Santos FS, Seigler DS, Silva GS, Simon MF, Soares MVB, Terra V (2024) Advances in Legume Systematics 14. Classification of Caesalpinioideae. Part 2: Higher-level classification. PhytoKeys 240: 1-552. https://doi.org/10.3897/phytokeys.240.101716

Figure 84 Distribution of Arapatiella based on quality-controlled digitised herbarium records. See Suppl. material 1 for the source of occurrence data.

opencc-by-4.0Apr 2024View details →
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FIGURE 84 in Systematics of the green lacewing tribe Ankylopterygini Navás, 1910 (Neuroptera: Chrysopidae: Chrysopinae) from China

FIGURE 84. Distribution map of species of Nineta from China.

opennotspecifiedNov 2024View details →
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Figure 3 from: Santos-Silva C, Louro R, Natário B, Nobre T (2021) Lack of knowledge on ecological determinants and cryptic lifestyles hinder our understanding of Terfezia diversity. MycoKeys 84: 1-14. https://doi.org/10.3897/mycokeys.84.71372

Figure 3 Terfezia species collected in the present work AT. arenariaBT. fanfaniCT. cistophilaDT. griseaET. dunensisFT. extremadurensisGT. lusitanicaHT. piniIT. solaris-libera.

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Figure 1 from: Santos-Silva C, Louro R, Natário B, Nobre T (2021) Lack of knowledge on ecological determinants and cryptic lifestyles hinder our understanding of Terfezia diversity. MycoKeys 84: 1-14. https://doi.org/10.3897/mycokeys.84.71372

Figure 1 a Phylogenetic relationship between Terfezia species. The reconstructed phylogeny corresponds to the majority rule consensus tree higher than 0.50 of trees sampled in a Bayesian analysis, and the posterior probability values are shown for main nodes b clades with new sequenced specimens collected within the present study.

opencc-by-4.0Oct 2021View details →
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Figure 2 from: Santos-Silva C, Louro R, Natário B, Nobre T (2021) Lack of knowledge on ecological determinants and cryptic lifestyles hinder our understanding of Terfezia diversity. MycoKeys 84: 1-14. https://doi.org/10.3897/mycokeys.84.71372

Figure 2 Phylogenetic reconstruction of intra-species diversity (Fig. 1) linking to soil properties and putative host plant aT. arenariabT. fanfanicT. grisea [specimens in the circle represent deviations from the ecological grouping, see text for details] dT. lusitanica. The other species are identified and their relation to soil and host plant are presented in the main text.

opencc-by-4.0Oct 2021View details →
zenodo28/100

Figure 1 from: Yang Q, Tang J, Zhou GY (2021) Characterization of Diaporthe species on Camellia oleifera in Hunan Province, with descriptions of two new species. MycoKeys 84: 15-33. https://doi.org/10.3897/mycokeys.84.71701

Figure 1 Phylogram of Diaporthe resulting from a maximum likelihood analysis based on combined ITS, cal, his3, tef1 and tub2. Numbers above the branches indicate ML bootstraps (left, ML BS ≥ 50%) and Bayesian Posterior Probabilities (right, BPP ≥ 0.75). The tree is rooted with Diaporthella corylina. Isolates in current study are in blue. "-" indicates ML BS < 50% or BI PP < 0.75.

opencc-by-4.0Oct 2021View details →
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Supplementary material 1 from: Santos-Silva C, Louro R, Natário B, Nobre T (2021) Lack of knowledge on ecological determinants and cryptic lifestyles hinder our understanding of Terfezia diversity. MycoKeys 84: 1-14. https://doi.org/10.3897/mycokeys.84.71372

Table S1

opencc-zeroOct 2021View details →
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Fig. 84. C. castanea Westwood, 1837 in Belgian Journal of Entomology

Fig. 84. C. castanea Westwood, 1837.

opennotspecifiedMay 2021View details →
zenodo28/100

Figure 1 from: Hurdeal VG, Gentekaki E, Hyde KD, Nguyen TTT, Lee HB (2021) Novel Mucor species (Mucoromycetes, Mucoraceae) from northern Thailand. MycoKeys 84: 57-78. https://doi.org/10.3897/mycokeys.84.71530

Figure 1 Maximum likelihood phylogram inferred from 102 taxa and 2017 characters based on ITS, and LSU matrix using GTR+G+I model and partition analysis. Maximum likelihood bootstrap support (≥ 70%) and Bayesian posterior probability (≥ 0.70) are indicated above the branches or near the nodes in this order. The tree is artificially rooted using Backusella dispersa (CBS 195.28), and B. grandis (CBS 186.87). The new species are in bold and the type species in the dataset are indicated using T. (-) represent bootstrap support lower than 70% or posterior probability lower than 0.70.

opencc-by-4.0Oct 2021View details →
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Figure 6 from: Lee BG, Hur J-S (2021) Two new calcicolous caloplacoid lichens from South Korea, with a taxonomic key to the species of Huriella and Squamulea. MycoKeys 84: 35-55. https://doi.org/10.3897/mycokeys.84.71227

Figure 6 Pyrenodesmia rugosa (BDNA-L-0001102, holotype) in morphology A–C habitus and apothecia. Rugose thallus brown with orange spots and without pruina, but black apothecia often white pruinose D–E zeorine apothecia with well-developed parathecium. Algal layers continue to the base and underlying the hypothecium F epihymenium K+ purple and tiny granules not dissolving in K G–K asci oblong to narrowly clavate with eight spores K in the lactophenol cotton blue L ascospores simple in the beginning and developed polarilocular at maturity M paraphyses anastomosing in lactophenol cotton blue. Paraphysis tips slightly swollen. Scale bars: 1 mm (A–C); 100 μm (D); 50 μm (E, F); 10 μm (G–M).

opencc-by-4.0Nov 2021View details →
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Figure 4 from: Lee BG, Hur J-S (2021) Two new calcicolous caloplacoid lichens from South Korea, with a taxonomic key to the species of Huriella and Squamulea. MycoKeys 84: 35-55. https://doi.org/10.3897/mycokeys.84.71227

Figure 4 Phylogenetic relationships amongst available species in the genus Pyrenodesmia , based on a Maximum Likelihood analysis of the dataset of the nuclear large subunit ribosomal RNA (LSU) sequences. The tree was rooted with three sequences of the genera Lendemeriella and Usnochroma. Maximum Likelihood bootstrap values ≥ 70% and posterior probabilities ≥ 95% are shown above internal branches. Branches with bootstrap values ≥ 90% are shown in bold. The new species Pyrenodesmia rugosa is presented in bold and all species names are followed by the GenBank accession numbers. Reference Table 1 provides the species related to the specific GenBank accession numbers and voucher information.

opencc-by-4.0Nov 2021View details →
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Figure 5 from: Lee BG, Hur J-S (2021) Two new calcicolous caloplacoid lichens from South Korea, with a taxonomic key to the species of Huriella and Squamulea. MycoKeys 84: 35-55. https://doi.org/10.3897/mycokeys.84.71227

Figure 5 Phylogenetic relationships amongst available species in the genera Huriella and Squamulea, based on a Maximum Likelihood analysis of the dataset of ITS sequences. The tree was rooted with the sequences of the genera Amundsenia, Erichansenia and Shackletonia. Maximum Likelihood bootstrap values ≥ 70% and posterior probabilities ≥ 95% are shown above internal branches. Branches with bootstrap values ≥ 90% are shown in bold. The new species Huriella aeruginosa is presented in bold and all species names are followed by the GenBank accession numbers. Reference Table 1 provides the species related to the specific GenBank accession numbers and voucher information.

opencc-by-4.0Nov 2021View details →
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Figure 7 from: Lee BG, Hur J-S (2021) Two new calcicolous caloplacoid lichens from South Korea, with a taxonomic key to the species of Huriella and Squamulea. MycoKeys 84: 35-55. https://doi.org/10.3897/mycokeys.84.71227

Figure 7 Huriella aeruginosa (BDNA-L-0001072, holotype) in morphology A–C habitus and apothecia. Thallus dark greenish-grey to grey with no pruina. Thalline margin of apothecia concolorous to disc D apothecia adnate or rarely sessile. Amphithecium well-developed, but parathecium inconspicuous. E thallus with dark green pigment layer under cortex F–G clavate asci containing 8-spores H ascospores generally ellipsoid, but occasionally globose, developing polarilocular in both types. Two blue coloured spores in lactophenol cotton blue. Scale bars: 1 mm (A–C); 100 μm (D);10 μm (E–H).

opencc-by-4.0Nov 2021View details →
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Figure 2 from: Lee BG, Hur J-S (2021) Two new calcicolous caloplacoid lichens from South Korea, with a taxonomic key to the species of Huriella and Squamulea. MycoKeys 84: 35-55. https://doi.org/10.3897/mycokeys.84.71227

Figure 2 Phylogenetic relationships amongst available species in the genus Pyrenodesmia, based on a Maximum Likelihood analysis of the dataset of ITS sequences. The tree was rooted with the sequences of the genera Caloplaca, Lendemeriella, Olegblumia and Usnochroma. Maximum Likelihood bootstrap values ≥ 70% and posterior probabilities ≥ 95% are shown above internal branches. Branches with bootstrap values ≥ 90% are shown in bold. The new species Pyrenodesmia rugosa is presented in bold and all species names are followed by the GenBank accession numbers. Reference Table 1 provides the species related to the specific GenBank accession numbers and voucher information.

opencc-by-4.0Nov 2021View details →

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