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1,790 results for “taxonomic status”
FIGURE 6 in The taxonomic status of Long-tailed shrews (Mammalia: genus Sorex) from Nuclear Central America
FIGURE 6. Plot of the Principal Component scores on the first two axes based on 12 log-transformed skull variables on specimens of S. chiapensis and the Sierra Madre of Guatemala.
FIGURE 4 in The taxonomic status of Long-tailed shrews (Mammalia: genus Sorex) from Nuclear Central America
FIGURE 4. Plot of the Principal Component scores on the first two axes based on 12 log-transformed skull variables for specimens identified as Sorex veraepacis species group (see Table 4).
FIGURE 3 in The taxonomic status of Long-tailed shrews (Mammalia: genus Sorex) from Nuclear Central America
FIGURE 3. Plot of Principal Component scores based on 12 log-transformed skull variables for specimens identified as Sorex salvini species group (see Table 3).
FIGURE 5 in The taxonomic status of Long-tailed shrews (Mammalia: genus Sorex) from Nuclear Central America
FIGURE 5. Plot of the Principal Component scores on the first two axes based on 8 log-transformed skull variables for specimens identified as Sorex veraepacis including the type specimen (see Table 5).
FIGURE 2. A in The taxonomic status of Long-tailed shrews (Mammalia: genus Sorex) from Nuclear Central America
FIGURE 2. A Plot of PCA scores on the first two Principal Component axes (see Table 2). Closed circles are specimens that do not possess a postmandibular foramen (the group to the upper right). Specimens possessing a postmandibular foramen are in the lower left of the graph.
FIGURE 1 in The taxonomic status of Long-tailed shrews (Mammalia: genus Sorex) from Nuclear Central America
FIGURE 1. Map of Nuclear Central America (southern Mexico and northern Central America) indicating the sample localities from which specimens of Sorex were examined. Only 36 localities are shown since several of the 53 recorded localities overlap on the map. The 1,000-m contour is shown.
FIGURE 3 in Morphological variation of Trilepida macrolepis (Peters 1857), with reappraisal of the taxonomic status of Rena affinis (Boulenger 1884) (Serpentes: Leptotyphlopidae: Epictinae)
FIGURE 3. Dorsal (A) and ventral (B) views of body and dorsal (C), lateral (D), and ventral (E) views of head of the lectotype of Trilepida macrolepis (ZMB 1434). Photos by F. Tillack (ZMB).
FIGURE 1 in Morphological variation of Trilepida macrolepis (Peters 1857), with reappraisal of the taxonomic status of Rena affinis (Boulenger 1884) (Serpentes: Leptotyphlopidae: Epictinae)
FIGURE 1. Dorsal (A), lateral (B), and ventral (C) views of the head of Trilepida affinis holotype (BMNH 75.2.26.4). The arrow shows the divided base of first supralabial scale. Scale = 5 mm. Photos by R. Fernandes (MNRJ).
FIGURE 2 in Morphological variation of Trilepida macrolepis (Peters 1857), with reappraisal of the taxonomic status of Rena affinis (Boulenger 1884) (Serpentes: Leptotyphlopidae: Epictinae)
FIGURE 2. Geographic distribution of Trilepida affinis (grid) and Trilepida macrolepis (circles). Type locality is represented by open symbol, examined specimens by close symbol and literature records by triangles.
FIGURE 4 in Morphological variation of Trilepida macrolepis (Peters 1857), with reappraisal of the taxonomic status of Rena affinis (Boulenger 1884) (Serpentes: Leptotyphlopidae: Epictinae)
FIGURE 4. General view of the paralectotypes of Trilepida macrolepis (A—ZMB 5294; B—ZMB 5722). Scale = 5 mm. Photos by F. Tillack (ZMB).
FIGURE 6 in The taxonomic status of two Telmatobius frog species (Anura: Telmatobiidae) from the western Andean slopes of northernmost Chile
FIGURE 6. Phylogenetic relationships between Chilean and Bolivian–Altiplanic Telmatobius species. Majority-rule consensus Bayesian tree. Black circles indicate the main groups proposed by Sáez et al. (2014). The white circle indicates the node that groups the new localities with T. pefauri and T. zapahuirensis. Statistical support (bootstrap and posterior probability) is given below or above the corresponding node (MP/ML/IB). Black boxes at the right of the tree denote groups (or clades), considered in the Discriminant Analysis (see Table 3).
FIGURE 5 in The taxonomic status of two Telmatobius frog species (Anura: Telmatobiidae) from the western Andean slopes of northernmost Chile
FIGURE 5. Results of the Principal Components (A & B) and Discriminant Analysis (C) using morphological measurements of Telmatobius specimens. The percentage of the variance explained is indicated in parentheses.
FIGURE 4 in The taxonomic status of two Telmatobius frog species (Anura: Telmatobiidae) from the western Andean slopes of northernmost Chile
FIGURE 4. Body color variation of live females of Telmatobius pefauri from Socoroma (A), Copaquilla (B), Belén (C), Lupica (D) and Saxamar (D). The color of the ventral surface is shown at the right for each case. The scale for the images are at the right.
FIGURE 3 in The taxonomic status of two Telmatobius frog species (Anura: Telmatobiidae) from the western Andean slopes of northernmost Chile
FIGURE 3. Specimen of Telmatobius pefauri DBGUCH-1501049 (topotype). A-on a rock in the Murmuntani valley; B-dorsal view; C-ventral view.
FIGURE 1 in The taxonomic status of two Telmatobius frog species (Anura: Telmatobiidae) from the western Andean slopes of northernmost Chile
FIGURE 1. Geographic distribution of Telmatobius populations of the western Andean slopes in the extreme north of Chile. Zapahuira and Murmuntani are the type localities of T. zapahuirensis and T. pefauri respectively.
FIGURE 2 in The taxonomic status of two Telmatobius frog species (Anura: Telmatobiidae) from the western Andean slopes of northernmost Chile
FIGURE 2. Specimen of Telmatobius pefauri DBGUCH-1501049 (topotype) fixed in formalin. A-lateral profile of the head; B-palmar view of the arm; C-dorsal view of the body; D-Plantar view of the foot.
FIGURE 7 in The taxonomic and phylogenetic status of some poorly known Anolis species from the Andes of Colombia with the description of a nomen nudum taxon
FIGURE 7. Maximum likelihood tree (-lnL=-13314.977) obtained with IQ-TREE depicting the phylogenetic relationships in the Andean species of the Anolis fuscoauratus species group. Inference based on 1465 characters of the ND2 gene and intervening regions. Nodal support was estimated using the ultrafast bootstrap method using 10000 pseudoreplicates (Minh et al., 2013).
FIGURE 8 in The taxonomic and phylogenetic status of some poorly known Anolis species from the Andes of Colombia with the description of a nomen nudum taxon
FIGURE 8. PCA plot of morphometric measurements from specimens of Anolis urraoi sp. nov. (red squares), A. mariarum (magenta circles), A. antonii (blue triangles), A. tolimensis (green diamonds) and some individuals tentatively assigned to A. mariarum (from Western Cordillera at Frontino National Park; black circles). PCA was performed with SVL (snout-vent length) and 22 morphological traits corrected for size (main text for details).
FIGURE 5 in The taxonomic and phylogenetic status of some poorly known Anolis species from the Andes of Colombia with the description of a nomen nudum taxon
FIGURE 5. Distribution map of the species in the Anolis fuscoauratus group included in this study. S and M indicate sequenced specimens and measured specimens respectively.
FIGURE 6 in The taxonomic and phylogenetic status of some poorly known Anolis species from the Andes of Colombia with the description of a nomen nudum taxon
FIGURE 6. Habitat of Anolis urraoi sp. nov. on the banks of the Penderisco river, Urrao, Antioquia, Colombia.
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OpenNeuro
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