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5 results for “Ophiognomonia”
Figure 4. Clade 3 in Host conservatism or host specialization? Patterns of fungal diversification are influenced by host plant specificity in Ophiognomonia (Gnomoniaceae: Diaporthales)
Figure 4. Clade 3 of the genus Ophiognomonia. Spatial evolutionary and ecological vicariance analysis (SEEVA) results. Divergence indices of four host plant variables: host plant order, family, genus, and species. Histograms of divergence indices (0–1) for each variable are mapped onto the maximum-likelihood tree from the GARLI analysis for 17 species of Ophiognomonia. After applying a Bonferroni correction (P ≤ 0.0034), the statistically significant divergence indices are indicated by asterisks at each node (*). Nodes are labelled as clade #:node #. The host plant families are represented as shaded boxes. The complete host–fungus associations are listed in Table 1. Patterns of host conservatism, specialization, or switching are indicated by bold arrows. Nodes 3:3, 3:4, 3:5, 3:9, 3:11, 3:12, 3:13, and 3:14 are not supported by maximum-likelihood bootstrap values of ≥ 70%.
Figure 2. Clade 1 in Host conservatism or host specialization? Patterns of fungal diversification are influenced by host plant specificity in Ophiognomonia (Gnomoniaceae: Diaporthales)
Figure 2. Clade 1 of the genus Ophiognomonia. Spatial evolutionary and ecological vicariance analysis (SEEVA) results. Divergence indices of four host plant variables: host plant order, family, genus, and species. Histograms representing divergence indices (0–1) for each variable are mapped onto the maximum-likelihood tree from the GARLI analysis for 16 species of Ophiognomonia. After applying a Bonferroni correction (P ≤ 0.0034), the statistically significant divergence indices are indicated by asterisks at each node (*). Nodes are labelled as clade #:node #. The host plant orders and families are represented as shaded boxes. The complete host–fungus associations are listed in Table 1. Patterns of host conservatism, specialization, or switching are indicated by bold arrows. Only node 1:15 is not supported by a maximumlikelihood bootstrap value of ≥ 70%.
Figure 1 in Host conservatism or host specialization? Patterns of fungal diversification are influenced by host plant specificity in Ophiognomonia (Gnomoniaceae: Diaporthales)
Figure 1. Morphology of the species Ophiognomonia alni-viridis. From the top, left to right: perithecia on an overwintered leaf of Alnus sinuata; single perithecium extracted from host tissue; single ascospore; and single ascus.
Figure 3. Clade 2 in Host conservatism or host specialization? Patterns of fungal diversification are influenced by host plant specificity in Ophiognomonia (Gnomoniaceae: Diaporthales)
Figure 3. Clade 2 of the genus Ophiognomonia. Spatial evolutionary and ecological vicariance analysis (SEEVA) results. Divergence indices of four host plant variables: host plant order, family, genus, and species. Histograms of divergence indices (0–1) for each variable are mapped onto the maximum-likelihood tree from the GARLI analysis for 14 species of Ophiognomonia. After applying a Bonferroni correction (P ≤ 0.0039), the statistically significant divergence indices are indicated by asterisks at each node (*). Nodes are labelled as clade #:node #. The host plant orders and families are represented as shaded boxes. The complete host–fungus associations are listed in Table 1. Patterns of host conservatism, specialization, or switching are indicated by bold arrows. All branches are supported by maximum-likelihood values ≥ 70%.
Data from: Host conservatism or host specialization? Patterns of fungal diversification are influenced by host plant specificity in Ophiognomonia (Gnomoniaceae, Diaporthales)
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