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373 results for “Crocodyliformes”
Fig. 3. A in First post-Mesozoic record of Crocodyliformes from Chile
Fig. 3. A. Indeterminate crocodilian right tibia (SGO−PV−833, Bahía Inglesa, Chile, late Miocene) in proximal (A1), medial (A2), and lateral (A3) aspects. Note the spiral fractures in A2 and A3. Such fractures involve torsional stress and indicate that the bone was fresh when the fracture occurred (see Lyman 1994 for a review of spiral fracture aetiology). Since impact during wave action or burial compaction seem unlikely to have caused the fracture, it may be direct evidence for predation or scavenging by other crocodyliforms. B. Indeterminate crocodilian tooth (SGO−PV−836, Bahía Inglesa, Chile, late Miocene). A1 and A2 are pencil drawings, A3 and B are photographs.
Fig. 2 in First post-Mesozoic record of Crocodyliformes from Chile
Fig. 2. Indeterminate crocodilian right dentary fragment (SGO−PV 834, Bahía Inglesa, Chile, late Miocene) in lateral (A), occlusal (B), medial (C), and caudal (D) aspects. Dashed line in white (in C) indicates position of Meckel's groove.
Fig. 1. A. Site location. B in First post-Mesozoic record of Crocodyliformes from Chile
Fig. 1. A. Site location. B. Generalised stratigraphic log of the Bahía Inglesa Formation. 1, Morro Member. Medium/coarse sands with Skolithos and crossbedding. Sands intercalated with coquinas, grading into pale fish−bearing siltstones to the north−east. Conglomerates present at some levels; 2, Bahía Inglesa Formation Bonebed Member. Phosphorites intercalated with fine/medium sands. The Bahía Inglesa Formation Bonebed marks the base; 3, Lechero Member. As Bahía Inglesa Formation Bonebed Member, but without phosphorites; 4, Early Pleistocene marine terrace downcuts toward bay. ssgc, sedimentary clast size division: silt, sand, gravel, and cobbles.
Fig. 9 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae
Fig. 9. The strict consensus of the five most parsimonious trees of Dyrosauridae found based on a cladistic analysis of 13 taxa and 30 characters (Appendices 1 and 2), and historical biogeography. Tree length: 44 steps long (C.I. excluding uninformative characters: 0.66; R.I.: 0.85; R.C.: 0.62). Land area abbreviations in the circles indicate optimised transformations on the tree, with two alternative results in light grey, and dark grey. Abbreviations: C, Congo; NAf, North Africa; NAm, North America; WAf, West Africa.
Fig. 8 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae
Fig. 8. Arambourgisuchus khouribgaensis gen. et sp. nov., Sidi Chenane, Morocco, late Palaeocene. Elements of mandibles. A. OCP DEK−GE 1200 in ventral view. B. OCP DEK−GE 269 in dorsal (B1) and lateral (B2) views. The arrows indicate the teeth that have been added recently, and which do not belong to the same specimen.
Fig. 5 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae
Fig. 5. Arambourgisuchus khouribgaensis gen. et sp. nov., OCP DEK−GE 300, Sidi Chenane, Morocco, late Palaeocene, detail of the right posttemporal fenestra in posterior view. Photograph (A) and explanatory drawing of the same (B).
Fig. 4 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae
Fig. 4. Arambourgisuchus khouribgaensis gen. et sp. nov., reconstruction of skull in dorsal (A) and ventral (B) views.
Fig. 6 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae
Fig. 6. Arambourgisuchus khouribgaensis gen. et sp. nov., OCP DEKGE 300, Sidi Chenane, Morocco, late Palaeocene, skull in occipital view. Photograph (A) and explanatory drawing of the same (B).
Fig. 3 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae
Fig. 3. Arambourgisuchus khouribgaensis gen. et sp. nov., OCP DEK−GE 18, Sidi Chenane, Morocco, late Palaeocene, skull and mandible in dorsal view. Photograph (A) and explanatory drawing of the same (B).
Fig. 1 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae
Fig. 1. Geographical position of the type locality. A. Geographical position of the Ouled Abdoun Basin (Morocco) in the Palaeocene deposit of Africa, (shaded area); modified from Capetta (1972). B. Simplified geological map of the Ouled Abdoun Basin; Sidi Chenane is the type locality (modified from Salvan 1952).
FIG. 8 in The youngest known South American dyrosaurid (Late Paleocene of Colombia), and evolution of Dyrosauridae (Crocodyliformes: Tethysuchia)
FIG. 8. — Comparison of taxic and phylogenetically corrected diversity with various extrinsic factors, such as proxies for temperatures, sea surface temperatures, and sea level: A, taxic and phylogenetically corrected diversity (dashed lines) (for data, see Appendix 3); B, δO18 data and mean and polynomial curves used as proxy for temperatures (Cramer et al. 2009; for data, see Appendix 4); C, mean temperatures (Grossman & Joachimski 2022; for data, see Appendix 5); D, δO18 data and mean and polynomial curves as proxies for sea surface temperatures (PhanSST global database, Judd et al. 2022; for data, see Appendix 6); E, sea level (Miller et al. 2005; for data, see Appendix 7).
FIG. 6 in The youngest known South American dyrosaurid (Late Paleocene of Colombia), and evolution of Dyrosauridae (Crocodyliformes: Tethysuchia)
FIG. 6. — Stratigraphical distribution of South and North American dyrosaurids. The possible Priabonian North American dyrosaurid is not figured.
FIG. 5 in The youngest known South American dyrosaurid (Late Paleocene of Colombia), and evolution of Dyrosauridae (Crocodyliformes: Tethysuchia)
FIG. 5. — Estimated length (star) based on measurements of centrum lengths and total lengths of 30 crocodylians (gray dots) by Iijima & Kubo (2020) (Appendix 2).
FIG. 7 in The youngest known South American dyrosaurid (Late Paleocene of Colombia), and evolution of Dyrosauridae (Crocodyliformes: Tethysuchia)
FIG. 7. — Geographical distribution of dyrosaurids from Late Cretaceous to middle Eocene. The Late Cretaceous map is represented by the Maastrichtian, the Paleocene by the Selandian, and the Lutetian-Bartonian by the Bartonian. Paleogeographic maps from Scotese (2014), modified from Markwick & Valdes (2004), Gayet et al. 1993, Boucot et al. 2013 and Jouve (2021). Circled numbers correspond to the number of species present in the locality. Yellow circle is the location of the specimen described herein
FIG. 3 in The youngest known South American dyrosaurid (Late Paleocene of Colombia), and evolution of Dyrosauridae (Crocodyliformes: Tethysuchia)
FIG. 3. — Outcrop, greenish gray mudstone where the vertebra UN-DG-Rp-1001 was collected, near the base of the Jacob's staff.
FIG. 4 in The youngest known South American dyrosaurid (Late Paleocene of Colombia), and evolution of Dyrosauridae (Crocodyliformes: Tethysuchia)
FIG. 4. — Actual (A, B) and 3D model (C-H) pictures of anterior dorsal (D4 or D5) vertebra UN-DG-Rp-1001 of the Piñalerita Section, Cuervos Formation (ThanetianYpresian). Views: A, anterior; B, right lateral; C, anterior; D, posterior; E, right lateral; F, left lateral; G, dorsal; H, ventral.Abbreviations: d, diapophysis; z, prezygapophysis; z', postzygapophysis; ns, neural spine; p, parapophysis; h, hypapophysis; ncs, neurocentral suture. The 3D model of the vertebra is provided in Appendix 1.
FIG. 1 in The youngest known South American dyrosaurid (Late Paleocene of Colombia), and evolution of Dyrosauridae (Crocodyliformes: Tethysuchia)
FIG. 1. — Geographical and geological context of the locality reported: A, localities with dyrosaurids in Colombia: Cerrejon Mine, Ortega (?) and Piñalerita Section (this study); B, geological map of the new locality, north of Sabanalarga town.
FIG. 3 in Un travail inédit de Jacques-Amand Eudes-Deslongchamps sur les crocodyliformes marins du Jurassique de Normandie
FIG. 3. — Dessin à l'encre (BCM Ms 640/6) représentant la mandibule et l'extrémité antérieure de la mâchoire supérieure du premier spécimen de Teleosaurus cadomensis tels qu'elles ont été dégagées par Eudes-Deslongchamps dans un des blocs acquis par Luard en novembre 1817. Des vues latérales et des vues en coupe des différents éléments sont également figurées. Dimensions de la feuille: 43,9 × 38,4 cm. © Bibliothèque centrale du Muséum national d'Histoire naturelle, Paris.
FIG. 1 in Un travail inédit de Jacques-Amand Eudes-Deslongchamps sur les crocodyliformes marins du Jurassique de Normandie
FIG. 1. — Première page de la première partie du manuscrit inédit de Jacques-Amand Eudes-Deslongchamps. Dimensions de la feuille: environ 15,5 × 19,5 cm. © American Philosophical Society, Philadelphie.
FIG. 2 in Un travail inédit de Jacques-Amand Eudes-Deslongchamps sur les crocodyliformes marins du Jurassique de Normandie
FIG. 2. — Première page de la deuxième partie du manuscrit inédit de Jacques-Amand Eudes-Deslongchamps. Dimensions de la feuille: environ 19,5 × 30 cm. © American Philosophical Society, Philadelphie.
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International Brain Laboratory public data
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OpenNeuro
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