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3,761 results for “phylogenetic relationship”
FIGURE 13 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 13. Non-stationary associations between phylogenetic diversity (AvPD) and annual range in temperature (TEMPr). The maps show the spatial variation in local beta coefficients (b) for TEMPr as predictor of AvPD, obtained from the full model, i.e., including all environmental predictors, after application of geographically weighted regression separately on data for each mammal group. Regions of (+) and negative (-) associations are indicated. Maps are in Mollweide equal-area projection. Dash lines on each map indicate the location of the tropics in the Northern and Southern Hemispheres.
FIGURE 12 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 12. Non-stationary associations between phylogenetic diversity (AvPD) and annual precipitation (PREC). The maps show the spatial variation in local beta coefficients (b) for PREC as predictor of AvPD, obtained from the full model, i.e., including all environmental predictors, after application of geographically weighted regression separately on data for each mammal group. Regions of (+) and negative (-) associations are indicated. Maps are in Mollweide equal-area projection. Dash lines on each map indicate the location of the tropics in the Northern and Southern Hemispheres.
FIGURE 10 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 10. Non-stationary associations between phylogenetic diversity (AvPD) and mean annual temperature (TEMP). The maps show the spatial variation in local beta coefficients (b) for TEMP as predictor of AvPD, obtained from the full model, i.e., including all environmental predictors, after application of geographically weighted regression separately on data for each mammal group. Regions of (+) and negative (-) associations are indicated. Maps are in Mollweide equal-area projection. Dash lines on each map indicate the location of the tropics in the Northern and Southern Hemispheres.
FIGURE 2 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 2. Spatial patterns of variation in the phylogenetic diversity (AvPD) of different mammal groups over the Americas. Maps are in Mollweide equal-area projection. Dash lines on each map indicate the location of the tropics in the Northern and Southern Hemispheres.
FIGURE 3 in Biogeographical affinity shapes relationships between ecological and phylogenetic mammal diversity and associations with their environmental correlates in the Americas
FIGURE 3. Non-stationary associations between ecological diversity (ED) and phylogenetic diversity (AvPD). The maps show the local beta coefficients (b) for AvPD as predictor of ED, obtained from the full model, i.e., including all environmental predictors and species richness (TR), after application of geographically weighted regression separately on data for each mammal group. Following (Matthews & Yang 2012) non-significant values (p> 0.05) are excluded from the maps to optimize the visualization of patterns. Regions of (+) and negative (-) associations are indicated. Maps are in Mollweide equal-area projection. Dash lines on each map indicate the location of the tropics in the Northern and Southern Hemispheres.
FIGURE Phylogenetic relationships of the Coelastrella genus inferred from the 18S-ITS1-5.8S-ITS2 region. The Neighbor-Joining (NJ), Maximum Likelihood (ML) bootstrap values and Bayesian posterior probabilities (PP) are presented at the nodes (NJ/ML/PP). Only values above 75 are shown. Strains provided in this study are indicated in bold font. Authentic strains marked with asterisks. The scale bar represents the number of substitutions per site. The GenBank accession numbers of Coelastrella can be found in the Table 3. in Morphological and phylogenetic relations of members of the genus Coelastrella (Scenedesmaceae, Chlorophyta) from the Ural and Khentii Mountains (Russia, Mongolia)
FIGURE Phylogenetic relationships of the Coelastrella genus inferred from the 18S-ITS1-5.8S-ITS2 region. The Neighbor-Joining (NJ), Maximum Likelihood (ML) bootstrap values and Bayesian posterior probabilities (PP) are presented at the nodes (NJ/ML/PP). Only values above 75 are shown. Strains provided in this study are indicated in bold font. Authentic strains marked with asterisks. The scale bar represents the number of substitutions per site. The GenBank accession numbers of Coelastrella can be found in the Table 3.
FIGURES 8–11 in Phylogenetic relationships of Elateridae inferred from adult morphology, with special reference to the position of Cardiophorinae
FIGURES 8–11. Dorsal view of scutellum of Cardiophorinae (scale bar = 0.5 mm). 8, Esthesopus castaneus; 9 Blaiseus bedeli; 10, Cardiophorus gramineus; 11, Negastrius americanus. Figure 12. Latero-ventral view of mesepimeron and mesepisternum of Cardiophorus fenestratus (LeConte) showing measurement of angle (a) of anterolateral corner of mesepisternum (scale bar = 0.5 mm). MST = mesepisternum; MRN = mesepimeron.
FIGURES. 5–6 in Phylogenetic relationships of Elateridae inferred from adult morphology, with special reference to the position of Cardiophorinae
FIGURES. 5–6. Latero-ventral view of hypomeron of Cardiophorinae (scale bar = 1 mm). 5, Cardiophorus gagates Erichson; 6, Cardiophorus propinquus Lanchester. Ant = anterior.
Figure 4 in Phylogenetic relationships of the pygmy rice rats of the genus Oligoryzomys Bangs, 1900 (Rodentia: Sigmodontinae)
Figure 4. Dispersal–vicariance analysis with geographic regions optimized onto the topology of the Bayesian consensus tree. The hypothetical ancestral distributions obtained through this method are listed above the branches.
Figure 3 in Phylogenetic relationships of the pygmy rice rats of the genus Oligoryzomys Bangs, 1900 (Rodentia: Sigmodontinae)
Figure 3. Oligoryzomys phylogeny based on weighted parsimony analysis (WP) and the Bayesian Markov Chain Monte Carlo method (BMCMC). The phylogeny was obtained for the combined mitochondrial cytochrome b and NADH1 sequence data, whereas BMCMC represents a consensus tree of the N = 21 950 trees from the converged Markov chain. A posterior probability above 0.5 and bootstrap values over 50% are represented on each node. C1 represents calibration time 1 = 1.5 Mya; C2 represents calibration time 2 = 0.24 Mya (according to Pardiñas et al., 2002; see Material and methods). Diamonds on nodes represent that clade number for the clock calibration using BEAST.
Figure 2 in Phylogenetic relationships of the pygmy rice rats of the genus Oligoryzomys Bangs, 1900 (Rodentia: Sigmodontinae)
Figure 2. Nucleotide-based pairwise distances calculated independently for each gene (A, cytochrome b; B, NADH1), vs. pairwise distances calculated from the concatenation of two genes (see Material and methods for the calculation of distances).
Figure 1A in Phylogenetic relationships of the pygmy rice rats of the genus Oligoryzomys Bangs, 1900 (Rodentia: Sigmodontinae)
Figure 1A. Approximate geographic distribution of species of the genus Oligoryzomys, including undescribed taxa Oligoryzomys sp. 1 and Oligoryzomys sp. B (the distribution of Oligoryzomys sp. B is according to trapping records reported in Carleton and Musser, 1989).
FIGURE 3. Phylogenetic relationships among Indosasa triangulata and other 17 in Pleioblastus triangulata (Poaceae: Bambusoideae), a new combination for Indosasa triangulata based on morphological and molecular evidence
FIGURE 3. Phylogenetic relationships among Indosasa triangulata and other 17 species belonging to Arundinarieae derived from Maximum Likelihood and Bayesian analysis. Numbers on the nodes are bootstrap values from 1000 replicates and posterior probabilities after 6,000,000 generations.
FIGURE. Phylogenetic relationships among species on Poaceae shown with synoptic phylogenetic tree constructed by MP method based on ITS+28S regions of rDNA. Same color branches show phylogenetic groups. 0, I: Spermogonial and aecial host genus. in Phylogenetic approach for identification and life cycles of Puccinia (Pucciniaceae) species on Poaceae from northeastern China
FIGURE. Phylogenetic relationships among species on Poaceae shown with synoptic phylogenetic tree constructed by MP method based on ITS+28S regions of rDNA. Same color branches show phylogenetic groups. 0, I: Spermogonial and aecial host genus.
FIGURE 40 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 40. NJ tree constructed based on cox1 genes. Gray shades color bars beside the tree indicate the delineated MOTUs by ABGD (K80-6) and jMOTU methods.
FIGURE 36. The secondary structures for 22 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 36. The secondary structures for 22 tRNA genes of the Capnogryllacris nigromarginata hainanensis ssp. nov..
FIGURE 35. The secondary structures for 22 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 35. The secondary structures for 22 tRNA genes of the Capnogryllacris nigromarginata rectispina ssp. nov..
FIGURE 34. The secondary structures for 22 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 34. The secondary structures for 22 tRNA genes of the Capnogryllacris nigromarginata nigromarginata.
FIGURE 32. The secondary structures for 22 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 32. The secondary structures for 22 tRNA genes of the Capnogryllacris erythrocephala maculatis ssp. nov..
FIGURE 30 in Contribution to the knowledge of Chinese Gryllacrididae (Orthoptera) V: Further study on the Chinese Capnogryllacris and comment on the phylogenetic relationships of the Gryllacrididae
FIGURE 30. Habitus of Capnogryllacris spp. A–C. Capnogryllacris spinosa (Li, Liu & Li, 2014); D. male of Capnogryllacris melanocrania (Karny, 1929).
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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