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249 results for “archosaurs”
Fig. 3. A in An unusual trackway of a possibly bipedal archosaur from the Late Triassic of the Sichuan Basin, China
Fig. 3. A. Overview of the Late Triassic Fushun archosaur trackway. Stitched photograph (A 1), interpretative outline drawing (A 2), pace lines connecting the reference points (intersection of long and wide axes) of each track (A 3). Note that the reference point of FS-11 is ambiguous, because the foot was possibly sliding backwards into FS-10. B. Eosauropus trackway from the Utah West tracksite (Lockley et al. 2011: fig. 6). C. Eosauropus trackway from the Knowles Canyon tracksite (Lockley et al. 2011: fig. 6).
Fig. 6 in An unusual trackway of a possibly bipedal archosaur from the Late Triassic of the Sichuan Basin, China
Fig. 6. Comparison of the Fushun archosaur trackway with Pseudotetrasauropus, Otozoum, and Eosauropus. A. Outline drawing of the right pes FS-12 of the Fushun trackway. B. Pseudotetrasauropus bipedoida Ellenberger, 1972 (modified from D'Orazi Porchetti and Nicosia 2007: fig. 9). C. Otozoum moodii Rainforth, 2003 (mirrored and modified from Rainforth 2003: fig. 3C). D. Eosauropus cimarronensis Lockley, Lucas, and Hunt, 2006 (Lockley et al. 2006a: fig. 4A). In B 2, C 2 the gray-scale sketches show the connected outer edges; the black bars the length of the four digits. The digits of P. bipedoida are well separated while those of O. moodii are relatively compact. However, during foot withdrawal out of deep substrate, both could result in the anterior, elongated grooves as observed in FS-12, and these could correspond to digits III and IV.
Fig. 5 in An unusual trackway of a possibly bipedal archosaur from the Late Triassic of the Sichuan Basin, China
Fig. 5. Close-up photographs highlighting characteristic the Late Triassic Fushun archosaur track features. A. Photograph (A 1) and outline drawing A 2) of FS-5 exhibiting a large impression at the rear of the track, which is inclined towards the deepest part of the track, and a two elongated grooves in the anterior part of the track. The impression at the rear of the track is interpreted as being related to the foot sliding on the substrate into its final position, and the two elongated anterior grooves as toe and claw drag marks after foot withdrawal. B. Low-angle light photograph of FS-5 and FS-6. Note the two elongated grooves in the anterior part of FS-5, interpreted as toe and claw drag marks. C. Straight and washed out grooves between FS-6 and FS-7, and FS-7 and FS-8, interpreted as erosional dissolution features around roots and/or of draining water. Arrows indicate walking direction.
Fig. 1 in The taxonomy and anatomy of rauisuchian archosaurs from the Late Triassic of Germany and Poland
Fig. 1. Right maxilla of rauisuchian Teratosaurus suevicus Meyer, 1861 from Mittlerer Stubensandstein, Upper Triassic of Heslach, Germany, NHM 38646, holotype. Photographs in lateral (A), medial (B), and ventral (C) views. Designation "m" refers to maxillary tooth position.
Fig. 2 in The taxonomy and anatomy of rauisuchian archosaurs from the Late Triassic of Germany and Poland
Fig. 2. Right maxilla of rauisuchian Teratosaurus suevicus Meyer, 1861 from Mittlerer Stubensandstein, Upper Triassic of Heslach, Germany, NHM 38646, holotype. Photographs in medial (A) and anterior (B) views. A is a close−up of the medial surface of the anterior end of the maxilla. Designation "m" refers to maxillary tooth position.
Fig. 3 in The taxonomy and anatomy of rauisuchian archosaurs from the Late Triassic of Germany and Poland
Fig. 3. Left maxilla of rauisuchian Polonosuchus silesiacus (Sulej, 2005) from Late Carnian, Upper Triassic of Krasiejów Claypit, Poland, ZPAL AbIII/563, part of holotype. Photographs in lateral (A), medial (B), and ventral (C) views. Designation "m" refers to maxillary tooth position.
Fig. 7 in A large predatory archosaur from the Late Triassic of Poland
Fig. 7. Comparison of the morphology and sizes of femur bones of the Late Triassic archosaurs (all in anterior views). A. Femur of Smok wawelski gen. et sp. nov., ZPAL V.33/45, Lisowice (Lipie Śląskie clay−pit), Late Triassic (lates Norian–early Rhaetian). B. Femur of Liliensternus liliensterni (Huene, 1934), MB.R.2175.7.1, Grossen Gleichberg, Germany, Late Triassic (early Rhaetian). C. Femur of Postosuchus kirckparicki Chatterjee, 1985, TTU− P9002, Miller's Ranch Quarry, Texas, USA (Norian).
Fig. 6. A in A large predatory archosaur from the Late Triassic of Poland
Fig. 6. A predatory archosaur Smok wawelski gen. et sp. nov., Lisowice (Lipie Śląskie clay−pit), Late Triassic (lates Norian–early Rhaetian). Isolated teeth in lateral view. A. ZPAL V.33/55. B. ZPAL V.33/50.
Fig. 4. A in A large predatory archosaur from the Late Triassic of Poland
Fig. 4. A predatory archosaur Smok wawelski gen. et sp. nov., Lisowice (Lipie Śląskie clay−pit), Late Triassic (lates Norian–early Rhaetian). A. Right premaxilla, ZPAL V.33/19, in lateral view. B. Left maxilla, ZPAL V.33/20, in lateral view. C. Left jugal, ZPAL V.33/97, in lateral view. D. Left frontal, ZPALV.33/21, in dorsal view. E. Left parietal, ZPAL V.33/98, in dorsal view.
Fig. 5. A in A large predatory archosaur from the Late Triassic of Poland
Fig. 5. A predatory archosaur Smok wawelski gen. et sp. nov., Lisowice (Lipie Śląskie clay−pit), Late Triassic (lates Norian–early Rhaetian). Pelvic girdle with sacrals (based on specimens ZPAL V.33/298, 300, 302–304), in posterior (A) and lateral (B) views.
Fig. 1 in A large predatory archosaur from the Late Triassic of Poland
Fig. 1. Field sketch showing distribution of Smok wawelski gen. et sp. nov. bones within the dark fine−grained mudstone lens at Lipie Śląskie clay−pit at Lisowice and their inferred routes of dislocation from the cadaver, presumably by scavengers or by water currents. Particular bone outlines are enlarged to show their orientation. Large tridactyl footprints were found somewhat above this level and outside the mapped area.
Fig. 3. A in A large predatory archosaur from the Late Triassic of Poland
Fig. 3. A predatory archosaur Smok wawelski gen. et sp. nov., Lisowice (Lipie Śląskie clay−pit), Late Triassic (lates Norian–early Rhaetian). Partially preserved braincase, ZPAL V.33/15, in left lateral (A) and dorsal views (B). Note that the right exoccipital−opisthotic, which is preserved as a separate piece, is not shown in the photo but is depicted in the reconstruction drawing in Fig. 2D.
Fig. 2. A in A large predatory archosaur from the Late Triassic of Poland
Fig. 2. A predatory archosaur Smok wawelski gen. et sp. nov., Lisowice (Lipie Śląskie clay−pit), Late Triassic (lates Norian–early Rhaetian). A. Skeletal restoration. B. Right dentary, ZPAL V.33/25, in lateral view. C. Left femur ZPAL V.33/45 in lateral (C1) and cranial views (C2). D. Reconstruction of partially preserved braincase ZPAL V.33/15,16, in dorsal (D1), left lateral (D2), and ventral (D3) views.
Fig. 61 in The Early Evolution Of Archosaurs: Relationships And The Origin Of Major Clades
Fig. 61. The distribution of Anisian suchians illustrating that the clade was distributed throughout Pangaea early in the evolution of Archosauria. Multiple suchian taxa are present in the Moenkopi Formation and the Manda Beds. Palaeogeographic globe after http://jan.ucc.nau.edu/,rcb7/globaltext2. html.
Fig. 59 in The Early Evolution Of Archosaurs: Relationships And The Origin Of Major Clades
Fig. 59. Relationship between age rank and clade rank for the pectinate components of nonarchosaurian archosauriforms (A), pseudosuchians (B), and avian-line archosaurs (C) used in this analysis. SRC values calculated in PAST (Hammer et al., 2001).
Fig. 60 in The Early Evolution Of Archosaurs: Relationships And The Origin Of Major Clades
Fig. 60. Calcanea of Anisian suchians. A, Right calcaneum of a suchian (IVPP unnumbered; Young, 1964: fig. 60A) from the Upper Ehrmaying (5 Ermaying) Formation of China in proximal (left), lateral (middle), and ventral (right) views. B, Right calcaneum of a suchian (MSM 4673) from the Moenkopi Formation of western North America in proximal (left), lateral (middle), and ventral (right) views. C, Left calcaneum of an additional suchian (MSM 4672) from the Moenkopi Formation of western North America in proximal (left), lateral (middle), and ventral (right) views. D, Partial left calcaneum of a suchian (NMT RB39) from the Manda Beds of southeastern Africa in proximal (left), anterior (middle), and ventral (right) views. Anatomical abbreviations in the appendix. Scale bars 5 1 cm.
Fig. 58. A in The Early Evolution Of Archosaurs: Relationships And The Origin Of Major Clades
Fig. 58. A, time-calibrated phylogeny of archosauriforms based on the relationships found in the phylogeny presented in figure 51. Timescale based on Gradstein et al. (2004) with the recent modifications of Muttoni et al. (2004, 2009), Mundil et al. (2004, 2010), Furin et al. (2006), and Schaltegger et al. (2008). The black bars represent ranges of clades whereas white boxes represent the possible range of taxa. Short dashed line 5 lineages that diverged by the end of the Early Triassic. Long dashed line 5 lineages that diverged by the end of the Anisian. Abbreviations: PERM 5 Permian; Ind 5 Induan; Olen 5 Olenekian.
Fig. 57 in The Early Evolution Of Archosaurs: Relationships And The Origin Of Major Clades
Fig. 57. The possible pylogenetic positions of Lewisuchus and Pseudolagosuchus when both taxa are kept as separate terminal taxa (A–C) compared to the result when Lewisuchus and Pseudolagosuchus are combined in a single terminal taxon (D).
Fig. 56 in The Early Evolution Of Archosaurs: Relationships And The Origin Of Major Clades
Fig. 56. Different clades previously proposed to be the sister taxon of Crocodylomorpha. The numbers represent how many additional steps it would take to make these clades the sister taxon of Crocodylomorpha.
Fig. 55 in The Early Evolution Of Archosaurs: Relationships And The Origin Of Major Clades
Fig. 55. Relationships of Poposauroidea. The distribution of a ''sail'' (silhouette of the skeleton) and endentulism (drawing of the skull) is complex. A ''sail'' either evolved twice in poposauroids, once in Arizonsaurus + Xilousuchus, and once in Lotosaurus or the ''sail'' was lost independently in Poposaurus and Shuvosauridae.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.