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369 results for “Cranial morphology”

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FIG. 4 in Cranial Morphology And Phylogenetic Relationships Of Trigonostylops Wortmani, An Eocene South American Native Ungulate

FIG. 4. Astrapotherium magnum AMNH VP-9278: A, ventral, B, dorsal, C, caudal, and D, right lateral views. Specimen is somewhat distorted and partly restored (see text). Apart from size, most noticeable external differences between Astrapotherium and Trigonostylops are concentrated in facial region (relative size of nasals and nasal cavity, rostral dentition, scale of pneumatization). Basicranial regions are also markedly different, but they share unusual derived features not found in non-astrapothere SANUs (see figs. 13–15, 27).

opencc-by-4.0Apr 2021View details →
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FIG. 1 in Cranial Morphology And Phylogenetic Relationships Of Trigonostylops Wortmani, An Eocene South American Native Ungulate

FIG. 1. Trigonostylops wortmani AMNH VP-28700, skull: A, ventral; B, dorsal; C, right lateral; D, left lateral; and E, caudal views (on this and facing page). In A, rectangle encloses palatal alate process (see fig. 20). For details of orbital and basicranial regions, see figures 25 and 26.

opencc-by-4.0Apr 2021View details →
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FIG. 3 in Cranial Morphology And Phylogenetic Relationships Of Trigonostylops Wortmani, An Eocene South American Native Ungulate

FIG. 3. Trigonostylops wortmani. Top: Mandible (MPEF PV 5483) with dentition: A, occlusal, B, rostral (mesial), and C, right lateral views. D, Reconstructed skull in right lateral aspect, chiefly based on AMNH 28700, MLP 52-X-5-98, and MPEF PV 5483.

opencc-by-4.0Apr 2021View details →
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Figure 9. A in Cranial morphology and dietary habits of rodents

Figure 9. A, log-log plot of the square root of cheek tooth area (√TA) vs. centroid size (dorsal), regression line: y = -1.220 + 1.216x, standard error of the estimate = 0.088, correlation coefficient r = 0.945, dashed reference line represents isometric scaling: y = -1.220 + x. B, plot of relative cheek tooth area [(√TA)/skull length] versus first canonical variate scores. Individual points represent species averages. Numbers associated with each point identify individual species in Appendix 1.

opencc-by-4.0Aug 2009View details →
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Figure 1 in Cranial morphology and dietary habits of rodents

Figure 1. Landmarks indicated on: A, dorsal, B, left lateral, and C, ventral views of the skull of Castor canadensis. Definitions of landmarks are included in Table 3.

opencc-by-4.0Aug 2009View details →
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Figure 8 in Cranial morphology and dietary habits of rodents

Figure 8. Box plots of incisor shape for dietary categories. A, incisor anteroposterior (AP) diameter divided by transverse (T) diameter. B, incisor procumbency angle. Bars display the mean, boxes represent the standard deviation, and whiskers represent the extreme values for each dietary group. Numbers associated with outliers identify individual species in Appendix 1.

opencc-by-4.0Aug 2009View details →
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Figure 10 in Cranial morphology and dietary habits of rodents

Figure 10. Skulls of selected members of the Muridae, illustrating some differences in cranial and dental structure associated with different diets. Each skull is scaled to the same total length. Scale bars with each skull represent 10 mm.

opencc-by-4.0Aug 2009View details →
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Figure 2. A in Cranial morphology and dietary habits of rodents

Figure 2. A, linear, and B, angular measurements illustrated on the skull of Castor canadensis. Note: although measurements are only illustrated for P4, all premolars and molars were measured.

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Figure 7 in Cranial morphology and dietary habits of rodents

Figure 7. Plot of first (CV1) and second (CV2) canonical variates; included are thin-plate splines for maximum observed deformations in each of the three views of the skull along each canonical axis. This figure is identical to Fig. 5 except that extinct rodent taxa with inferred diets are also included. Individual points represent the average shape for each species. Numbers associated with each point identify individual species in Appendix 1.

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Figure 3 in Cranial morphology and dietary habits of rodents

Figure 3. Relative warp plots for the dorsal, lateral, and ventral views of the skull. A, first (DRW1) and third (DRW3) dorsal relative warps, B, first (LRW1) and fourth (LRW4) lateral relative warps, C, first (VRW1) and second (VRW2) ventral relative warps. Individual points represent the average shape for each species. Numbers associated with each point identify individual species in Appendix 1. Shape deformations associated with each axis are illustrated in Fig. 4.

opencc-by-4.0Aug 2009View details →
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Figure 6 in Cranial morphology and dietary habits of rodents

Figure 6. Plot of first (CV1) and third (CV3) canonical variates; included are thin-plate splines for maximum observed deformations in each of the three views of the skull along each canonical axis. Individual points represent the average shape for each species. Numbers associated with each point identify individual species in Appendix 1.

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Figure 5 in Cranial morphology and dietary habits of rodents

Figure 5. Plot of first (CV1) and second (CV2) canonical variates; included are thin-plate splines for maximum observed deformations in each of the three views of the skull along each canonical axis. Individual points represent the average shape for each species. Numbers associated with each point identify individual species in Appendix 1.

opencc-by-4.0Aug 2009View details →
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Figure 5. Comparative cranial morphology for derived metriorhynchid species. A in What is Geosaurus? Redescription of Geosaurus giganteus (Thalattosuchia: Metriorhynchidae) from the Upper Jurassic of Bayern, Germany

Figure 5. Comparative cranial morphology for derived metriorhynchid species. A, Dakosaurus maximus neotype, SMNS 8203. B, Enaliosuchus schroederi holotype, MMGLV. C, Geosaurus araucanensis holotype, MLP 72-IV-7-1. The relative position of the orbit is indicated for Dakosaurus. Scale bars: 20 mm.

opencc-by-4.0Oct 2009View details →
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Figure 11 in Cranial morphology of Bachia bicolor (Squamata: Gymnophthalmidae) and its postnatal development

Figure 11. Right orbitosphenoid of neonate in dorsal view. Anterior to the top (UIS-R-1452). A, photograph. B, schematic drawing where cartilage is represented in black; mineralization of membranous ossifications is represented in grey, and endochondral ossification is represented in white. Scale bar = 0.25 mm.

opencc-by-4.0Apr 2008View details →
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Figure 8 in Cranial morphology of Bachia bicolor (Squamata: Gymnophthalmidae) and its postnatal development

Figure 8. Neonate skull and mandible of Bachia bicolor (UIS-R-1452). White dotted areas denote cartilage; black dotted areas denote scattered mineralization, suggesting membranous ossification. A, skull, lateral view. B, skull, ventral view. C, skull, dorsal view. D, mandible, lingual view. E, mandible, labial view. Key: ar, articular bone; bcf, basicranial fenestra; et, egg tooth; frpf, frontoparietal fontanelle; mc, Meckel's cartilage; nc, nasal cupola; or, orbitosphenoid; pa, processus ascendens of the tectum synoyicum; potf, post-temporal fossa; sa, surangular; sap, spheno-occipital tubercle apophyseal ossification; tc, trabecula communis. Scale bar = 1 mm.

opencc-by-4.0Apr 2008View details →
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Figure 9 in Cranial morphology of Bachia bicolor (Squamata: Gymnophthalmidae) and its postnatal development

Figure 9. Progressive closure of the frontoparietal fontanelle fusion of frontals and parietals, and the differentiation of the frontoparietal suture during postnatal development. White dotted areas denote mineralization, suggesting membranous ossification in the neonate. The fontanelle is highlighted in grey. A, neonate (UIS-R-1452). B, UISR-1451. C, UISR-1245. D, full-grown adult (UIS-R-1442). Scale bar = 1 mm.

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Figure 6. Palatal bones. A in Cranial morphology of Bachia bicolor (Squamata: Gymnophthalmidae) and its postnatal development

Figure 6. Palatal bones. A, vomer, dorsal view. B, vomer, lateral view. C, articulated vomer and septomaxilla in lateral view. D, articulated vomer and septomaxilla in ventral view. E, articulated palatine and pterygoid in dorsal view. Key: ap, anterior process; al, anterolateral process; cf, columellar fossa; dc, dorsal crest; fjo, fenestra for the Jacobson's organ; lp, lateral process; mp, maxillary process; plp, posterolateral process; pmp, posteromedial process; ptp, pterigoid process; qp, quadrate process; smx, septomaxilla; tf, transverse flange; tp, transverse process; v, vomer; vc, ventral crest; vp, vomerine process. Scale bar = 1 mm.

opencc-by-4.0Apr 2008View details →
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Figure 10 in Cranial morphology of Bachia bicolor (Squamata: Gymnophthalmidae) and its postnatal development

Figure 10. Progressive ossification of the trabecular cartilage and the cartilage trabecula communis, showing morphological intraspesific variation in the basisphenoid rostrum during postnatal development. Ventral view. A, neonate (UIS-R-1452). B, UIS-R-1451. C, UISR-1443. D, UISR-1437. E, full ossified adult (UIS-R-1453). Scale bar = 0.5 mm.

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Figure 4 in Cranial morphology of Bachia bicolor (Squamata: Gymnophthalmidae) and its postnatal development

Figure 4. Overlapped surfaces of nasal, frontal, and parietal in dorsal view, denoted by dashed lines. Key: frf, frontal facets on the parietal; ns, nasal shelves; tp, triangular processes. Scale bar = 1 mm.

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Figure 2 in Cranial morphology of Bachia bicolor (Squamata: Gymnophthalmidae) and its postnatal development

Figure 2. The hyoid apparatus of Bachia bicolor. Dotted areas denote cartilage. Key: b, basihyal; cbI, first ceratobranchial; eh, epihyal; hc, hyoid cornus; pl, processus lingualis. Scale bar = 1 mm.

opencc-by-4.0Apr 2008View details →

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