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39 results for “Anomodontia”
Figure 9 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 9. Drawing of the right forelimb of Suminia getmanovi (PIN 2212/62) in ventral view. Refer to the text for the abbreviations list. Scale bar: 1 cm.
Figure 10 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 10. Drawing of right humerus of Suminia getmanovi in ventral view as preserved in specimen 15 on the block (PIN 2212/116). Refer to the text for the abbreviations list. Scale bar: 1 cm.
Figure 5 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 5. Drawing of the pelvic region of Suminia getmanovi (specimen 2 on block PIN 2212/116). Refer to the text for the abbreviations list. Scale bar: 1 cm.
Figure 7 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 7. Photograph of the gastralia of Suminia getmanovi in ventral view, as preserved in specimen 5 on the block (PIN 2212/116). Scale bar: 1 cm.
Figure 6 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 6. Drawing of the caudal region of Suminia getmanovi (specimen 2 on block PIN 2212/116). Refer to the text for the abbreviations list. Scale bar: 1 cm.
Figure 8 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 8. Reconstruction of (A) the pectoral girdle and (B) the pelvic girdle of Suminia getmanovi in right lateral views. Refer to the text for the abbreviations list. Scale bar: 1 cm.
Figure 3 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 3. Drawing of the cervical region of Suminia getmanovi in (A) PIN 2212/104a (dorsal aspect), (B) PIN 2212/62 (lateral aspect), and (C) specimen 4 on block PIN 2212/116 (dorsal aspect). Refer to the text for the abbreviations list. Scale bar: 1 cm.
Figure 4 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 4. Drawing of the pectoral region of Suminia getmanovi (specimen 3 on block PIN 2212/116). Refer to the text for the abbreviations list. Scale bar: 1 cm.
Figure 2 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 2. Drawing of one of the best-preserved and most complete skeletons of Suminia getmanovi (specimen 1 on block PIN 2212/116) in dorsal view. Refer to the text for the abbreviations list. Scale bar: 2 cm.
Figure 1 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 1. Photograph (A) and colour-coded outline drawing (B) of specimens of Suminia getmanovi on the large block (PIN 2212/116).
Figure 14 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 14. Drawing of the left pes of Suminia getmanovi (holotype, PIN 2212/10) in ventral view. Refer to the text for the abbreviations list. Scale bar: 1 cm.
Figure 12 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 12. Reconstruction of (A) the right manus and (B) the right pes of Suminia getmanovi in dorsal views. Refer to the text for the abbreviations list. Scale bar: 1 cm.
Figure 1 in Do extraordinarily high growth rates in Permo-Triassic dicynodonts (Therapsida, Anomodontia) explain their success before and after the end-Permian extinction?
Figure 1. Stratigraphical ranges of the anomodonts used in this study. Modified from Angielczyk & Kurkin (2003) and Angielczyk & Walsh (2008). Oudenodon range updated from Botha & Angielczyk (2007). Kingoria is now referred to as Dicynodontoides following Angielczyk et al. (2009). Vertical solid bars and open bars indicate ranges and ghost lineages, respectively. Abbreviations: Chsn, Changhsingian; Ciste., Cistecephalus Assemblage Zone; Eodicyn., Eodicynodon Assemblage Zone; Ind., Induan; Lystro., Lystrosaurus; Olen., Olenekian; Prist., Pristerognathus Assemblage Zone; PTB, Permo-Triassic boundary; Tap., Tapinocephalus Assemblage Zone; Tropid. Tropidostoma Assemblage Zone; Wn, Wordian. Numbers indicate million years ago. Stratigraphical chart follows Catuneanu et al. (2005).
Figure 4. Permo-Triassic dicynodont bone histology. A in Do extraordinarily high growth rates in Permo-Triassic dicynodonts (Therapsida, Anomodontia) explain their success before and after the end-Permian extinction?
Figure 4. Permo-Triassic dicynodont bone histology. A, juvenile Dicynodon humerus SAM-PK-K5576d; B, subadult Dicynodon humerus NMQR3633a; C, subadult Lystrosaurus maccaigi ulna NMQR3663b; D, juvenile Lystrosaurus declivis tibia NMQR735b; D, E, adult Lystrosaurus humerus (possibly Lystrosaurus declivis) NMQR3678; F, late subadult Kannemeyeria femur NMQR2674b. Arrows indicate enlarged channels in all genera. Scale bars: D, E = 500 mm; A, B, C, F = 413 mm.
Figure 6. Permo-Triassic eutherapsid bone histology. A in Do extraordinarily high growth rates in Permo-Triassic dicynodonts (Therapsida, Anomodontia) explain their success before and after the end-Permian extinction?
Figure 6. Permo-Triassic eutherapsid bone histology. A, subadult gorgonopsian Scylacops femur SAM-PK-10188; B, adult therocephalian Pristerognathus femur SAM-PK-11557; C, late subadult nonmammalian cynodont Cynognathus femur SAM-PK-K6235a; D, early subadult nonmammalian cynodont Diademodon ulna SAM-PK-K8971c. Enlarged channels are absent from these taxa. Arrows indicate growth rings. Scale bars: B, D = 500 mm; A, C = 413 mm.
Figure 3. Permo-Triassic dicynodont bone histology. A, subadult Cistecephalus ulna NMQR1465b in Do extraordinarily high growth rates in Permo-Triassic dicynodonts (Therapsida, Anomodontia) explain their success before and after the end-Permian extinction?
Figure 3. Permo-Triassic dicynodont bone histology. A, subadult Cistecephalus ulna NMQR1465b; B, early subadult Dicynodontoides tibia NMQR479a; C, adult Rhachiocephalus ulna SAM-PK-3714a; D, subadult Tropidostoma tibia SAM-PK-K9960c; E, adult Oudenodon femur SAM-PK-K4807a; F, adult Aulacephalodon femur NMQR3016. Arrows indicate enlarged midcortical channels in Rhachiocephalus and Aulacephalodon. Scale bars: A, D, E = 500 mm; B, C, F = 413 mm.
Figure 16 in The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod
Figure 16. Skeletal reconstruction and body outline of the basal anomodont Suminia getmanovi.
Figure 5 in Do extraordinarily high growth rates in Permo-Triassic dicynodonts (Therapsida, Anomodontia) explain their success before and after the end-Permian extinction?
Figure 5. Phylogenetic distribution of mean channel density and enlarged vascular channels amongst therapsids. Mean channel density optimized using squared-change parsimony and equal branch lengths; enlarged vascular channels optimized using parsimony. Topology modified from Angielczyk (2007), Botha, Abdala & Smith (2007), Fröbisch (2007), and Liu, Li & Cheng (2002), Higher level taxonomy of anomodonts follows Kammerer & Angielczyk (2009).
Figure 2. Permian dicynodont bone histology. A in Do extraordinarily high growth rates in Permo-Triassic dicynodonts (Therapsida, Anomodontia) explain their success before and after the end-Permian extinction?
Figure 2. Permian dicynodont bone histology. A, adult Galeops humerus SAM-PK-12261a; B, early subadult Eodicynodon femur NMQR2996a; C, late subadult Eodicynodon femur NMQR3153a; D, late subadult Diictodon SAM-PK-K7725; E, subadult Endothiodon tibia SAM-PK-5605c; F, adult Endothiodon humerus SAM-PK-K6618a. Arrows indicate enlarged midcortical channels. Enlarged channels are absent in Galeops, Diictodon, and Endothiodon. However, subadult Endothiodon reveals rapid, sustained growth with an average channel area of 13%. Scale bars: B, C = 500 mm; A, D, E, F = 413 mm.
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