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14,185 results for “phylogenies”
Figure 9 in Phylogeny of the pollinating yucca moths, with revision of Mexican species (Tegeticula and Parategeticula; Lepidoptera, Prodoxidae)
Figure 9. Known locations for Tegeticula californica sp. nov. (squares) and T. baja sp. nov. (circles). Abbreviations: CA = California, BC = Baja California, BCS = Baja California Sur.
Figure 12 in Phylogeny of the pollinating yucca moths, with revision of Mexican species (Tegeticula and Parategeticula; Lepidoptera, Prodoxidae)
Figure 12. Maximum-likelihood-based reconstruction of the phylogenetic relationships among all recognized species of Tegeticula and Parategeticula, based on a 2104-bp region of mtDNA. Prodoxus y-inversus was used as outgroup. Taxa above arrow are members of the yuccasella complex. For details of analysis see text.
Figure 8 in Phylogeny of the pollinating yucca moths, with revision of Mexican species (Tegeticula and Parategeticula; Lepidoptera, Prodoxidae)
Figure 8. Parategeticula ecdysiastica sp. nov., female external genitalia. Ovipositor in (A) lateral view, (B) dorsolateral view, (C) ventral view, (D) dorsal view.
Figure 6 in Phylogeny of the pollinating yucca moths, with revision of Mexican species (Tegeticula and Parategeticula; Lepidoptera, Prodoxidae)
Figure 6. Ovipositor tip of (A) Tegeticula californica sp. nov. (CA: E Encenitas), (B) T. tehuacana sp. nov. (Pue. Zacatepec), (C) T. tambasi sp. nov. (Mich. San José Coapa), (D) T. baja sp. nov. (BCS. San Jacinto). Scale bar = 0.5 mm.
Figure 3 in Phylogeny of the pollinating yucca moths, with revision of Mexican species (Tegeticula and Parategeticula; Lepidoptera, Prodoxidae)
Figure 3. Pectinifer of (A) Tegeticula californica sp. nov. (CA: E Encenitas), (B) T. tehuacana sp. nov. (Pue. Acatepec), (C) T. tambasi sp. nov. (Mich. San José Coapa), (D) T. baja sp. nov. (BCS. W La Paz). For scale, see pectinifers in context in Figure 2.
Figure 3. Cossulinae phylogeny showing clade 3 in A revision of the Cossulinae of Costa Rica and cladistic analysis of the world species (Lepidoptera: Cossidae)
Figure 3. Cossulinae phylogeny showing clade 3; strict consensus of 27 trees, done in WinClada and NONA, L = 224, Ci = 32, Ri = 78; dark squares represent unique synapomorphies, empty squares represent homoplasious synapomorphies.
Figure 2. Cossulinae phylogeny showing clade 2 in A revision of the Cossulinae of Costa Rica and cladistic analysis of the world species (Lepidoptera: Cossidae)
Figure 2. Cossulinae phylogeny showing clade 2; strict consensus of 27 trees, done in WinClada and NONA, L = 224, Ci = 32, Ri = 78; dark squares represent unique synapomorphies, empty squares represent homoplasious synapomorphies.
Figure 1. Cossulinae phylogeny showing clade 1 in A revision of the Cossulinae of Costa Rica and cladistic analysis of the world species (Lepidoptera: Cossidae)
Figure 1. Cossulinae phylogeny showing clade 1; strict consensus of 27 trees, done in WinClada and NONA, L = 224, Ci = 32, Ri = 78; dark squares represent unique synapomorphies, empty squares represent homoplasious synapomorphies.
Figure 6 in Phylogeny and evolutionary history of the Aplodontoidea (Mammalia: Rodentia)
Figure 6. Phylogeny of aplodontoids using all ordered characters, with ordered characters down-weighted. Tree scores are listed in Table 2.
Figure 5 in Phylogeny and evolutionary history of the Aplodontoidea (Mammalia: Rodentia)
Figure 5. Phylogeny of aplodontoids using some ordered characters, with ordered characters down-weighted. Tree scores are listed in Table 2.
Figure 9 in Phylogeny and evolutionary history of the Aplodontoidea (Mammalia: Rodentia)
Figure 9. Aplodontine (Aplodontia rufa) molars, occlusal view. A, right lower molar (labial is down), showing B-shaped outline. B, left upper molar (lingual is down), showing shield-shaped outline.
Figure 10. Aplodontid P4s in Phylogeny and evolutionary history of the Aplodontoidea (Mammalia: Rodentia)
Figure 10. Aplodontid P4s showing anteroposterior widening of the protocone. A, Prosciurus left P4 with unexpanded protocone. B, indeterminate mylagaulid right P4, with expanded protocone.
Figure 3 in Phylogeny and evolutionary history of the Aplodontoidea (Mammalia: Rodentia)
Figure 3. Phylogeny of aplodontoids using some ordered characters, with ordered characters not down-weighted. Tree scores are listed in Table 2.
Figure 9. Mapped and reconstructed soldier head shapes positioned across a Termitidae phylogeny. Nodes a–g in Termite soldier defence strategies: a reassessment of Prestwich's classification and an examination of the evolution of defence morphology using extended eigenshape analyses of head morphology
Figure 9. Mapped and reconstructed soldier head shapes positioned across a Termitidae phylogeny. Nodes a–g are referred to in the text.
Figure 8 in Phylogeny and evolutionary history of the Aplodontoidea (Mammalia: Rodentia)
Figure 8. Phylogenetic position of poorly known taxa. The most likely points of insertion of poorly known taxa are indicated with circles. Multiple lines for a single taxon indicate multiple equally likely positions. Dashed lines that fork indicate that the two taxa are placed as sister taxa in the analysis. The poorly known species are as follows: 1, Prosciurus ordosicus Wang, 1987; 2, Prosciurus magnus Korth, 1989; 3, Prosciurus daxnerae Lopatin, 2000; 4, Ansomys crucifer Lopatin, 1997; 5, Ansomys shantungensis Rensberger & Li, 1986; 6, Parallomys argoviensis; 7, Allomys cristabrevis Barnosky, 1986; 8, Pseudaplodon asiatica Schlosser, 1924; 9, Sinomylagaulus halamagaiensis Wu, 1988; 10, Tschalimys ckhikvadzei Shevyreva, 1971.
Figure 7 in Phylogeny and evolutionary history of the Aplodontoidea (Mammalia: Rodentia)
Figure 7. Preferred phylogeny of aplodontid rodents. Solid lines represent the known stratigraphic range of taxa; thinner lines represent inferred ranges. Where the temporal ranges of taxa are poorly constrained, the entire possible range is included as the known stratigraphic range.
Figure 4 in Phylogeny and evolutionary history of the Aplodontoidea (Mammalia: Rodentia)
Figure 4. Phylogeny of aplodontoids using all ordered characters, with ordered characters not down-weighted. Tree scores are listed in Table 2.
Figure 1 in Phylogeny and evolutionary history of the Aplodontoidea (Mammalia: Rodentia)
Figure 1. Dental terminology used throughout this paper, illustrated on a range of aplodontid morphotypes. Anterior is to the left, labial is up for upper teeth (A, C, E, G, and I) and down for lower teeth (B, D, F, H, and J) A, upper molar of a basal aplodontid (Ansomys hepburnensis) showing major cusps and cingula. B, lower molar of a basal aplodontid (Ansomys hepburnensis) showing major cusps. C, same as (A), photographic image. D, same as (B), photographic image. E, P4 of a meniscomyine (Meniscomys uhtoffi) showing lophs and anterior cusps. F, P of an allomyine (Allomys magnus) 4 showing lophs of the lower teeth. G, same as (E), photographic image. H, same as (F), photographic image. I, P4 of a mylagaulid (Alphagaulus vetus) illustrating cusp homologies with other aplodontids. J, P4 of a mylagaulid (Alphagaulus vetus) illustrating cusp homologies.
Figure 2 in Phylogeny and evolutionary history of the Aplodontoidea (Mammalia: Rodentia)
Figure 2. Phylogeny of aplodontoids using all unordered characters. Tree scores are listed in Table 2.
Fig. 20. Most parsimonious cladogram for the 58 in Comparative Myology of Moles and the Phylogeny of the Talpidae (Mammalia, Lipotyphla)
Fig. 20. Most parsimonious cladogram for the 58 myological characters (CI = 0.82, RI = 0.90). Numbers identify clades, which are discussed in the text and used in the apomorphy list (table 4).
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Allen Brain Atlas
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