Trias

Laurasia during the closure of the Iapetus Ocean at 430 Ma. Made using GPlates: Citations: Golonka, J. (2007), Late Triassic and Early Jurassic palaeogeography of the world, Palaeogeography, Palaeoclimatology, Palaeoecology, 244(1-4), 297-307. Müller, R., M. Sdrolias, C. Gaina, and W. Roest (2008), Age, spreading rates, and spreading asymmetry of the world's ocean crust, Geochemistry, Geophysics, Geosystems, 9(Q04006), 19. Seton, M., R. Müller, S. Zahirovic, C. Gaina, T. Torsvik, G. Shephard, A. Talsma, M. Gurnis, M. Turner, and M. Chandler (2012), Global continental and ocean basin reconstructions since 200 Ma, Earth-Science Reviews, 113(3-4), 212-270. Torsvik, T., and R. Van de Voo (2002), Refining Gondwana and Pangea Palaeogeography: Estimates of Phanerozoic non dipole (octupole) fields, Geophysical Journal International, 151(3), 771-794. Wright, N., S. Zahirovic, R. D. Müller, and M. Seton (2013), Towards community-driven, open-access paleogeographic reconstructions: integrating open-access paleogeographic and paleobiology data with plate tectonics, Biogeosciences, 10, 1529-1541

Laurasia during the closure of the Iapetus Ocean at 430 Ma. Made using GPlates: Citations: Golonka, J. (2007), Late Triassic and Early Jurassic palaeogeography of the world, Palaeogeography, Palaeoclimatology, Palaeoecology, 244(1-4), 297-307. Müller, R., M. Sdrolias, C. Gaina, and W. Roest (2008), Age, spreading rates, and spreading asymmetry of the world's ocean crust, Geochemistry, Geophysics, Geosystems, 9(Q04006), 19. Seton, M., R. Müller, S. Zahirovic, C. Gaina, T. Torsvik, G. Shephard, A. Talsma, M. Gurnis, M. Turner, and M. Chandler (2012), Global continental and ocean basin reconstructions since 200 Ma, Earth-Science Reviews, 113(3-4), 212-270. Torsvik, T., and R. Van de Voo (2002), Refining Gondwana and Pangea Palaeogeography: Estimates of Phanerozoic non dipole (octupole) fields, Geophysical Journal International, 151(3), 771-794. Wright, N., S. Zahirovic, R. D. Müller, and M. Seton (2013), Towards community-driven, open-access paleogeographic reconstructions: integrating open-access paleogeographic and paleobiology data with plate tectonics, Biogeosciences, 10, 1529-1541

Various fossils pertaining to the holotype of the Triassic ichthyosaur Toretocnemus californicus. This image is derived from plate 24 in Merriam (1903), done by an uncredited artist. The arrangement of the individual figures has been modified from the original. Original description: Toretocnemus californicus n. gen. and sp. Figures reproduced natural size from the type specimen. Fig. 1. — Inferior side of right posterior limb. t, tibia. Fig. 2. — Right anterior limb. r, radius. Fig. 3.— Pelvic arch. Fig. 4. — Middle dorsal vertebrae and a rib from the same region.

Photograph of Museo civico di scienze naturali di Bergamo (MCSNB) 2888, the holotype specimen of Eudimorphodon ranzii ZAMBELLI 1973, a basal pterosaur from the Norian (middle Upper Triassic) of the Italian Alps.[1] ↑ see fig. 8A in Silvio Renesto (2006): A reappraisal of the diversity and biogeographic significance of the Norian (Late Triassic) reptiles from the Calcare di Zorzino. In: Jerry D. Harris, Spencer G. Lucas, Justin A. Spielmann, Martin G. Lockley, Andrew R.C. Milner, James I. Kirkland (eds.): The Triassic-Jurassic Terrestrial Transition. New Mexico Museum of Natural History and Science Bulletin 37:445–456 (online)

Thalattosaurus alexandrae (left) and Nectosaurus halinus (right) of Late Triassic California

A reconstruction of Erythrovenator jacuiensis based on a skeletal by Maurissauro. This basal theropod comes from the Late Triassic Candelária Formation of Brazil.

Ahvaytum is a saturnaliid sauropodomorph from the Late Triassic of what is now Wyoming. It is the oldest known dinosaur from the northern continent of Laurasia, challenging previous hypotheses of dinosaur origins and dispersal. Typical of basal dinosaurs from the Triassic, Ahvaytum was a small slender biped, reaching about 1 m in body length.

Holotype specimen (PIMUZ A/III 1274) of Prosantosaurus scheffoldi gen. et spec. nov. from the upper Prosanto Formation (Early Ladinian, Middle Triassic) of Ducanfurgga locality no. 4, southwest of Davos, Canton of Grisons, south-eastern Switzerland. A Nearly complete specimen as prepared in dorsal view. The posterior part of the tail was lost prior to burial. Both forearms are not visible but lie below the trunk region, pointing in an anteromedial direction (see Additional file 1: Fig. S3A). B Detail of skull and anterior neck region. C Outline sketch of skull sutures. D Detail of shoulder girdle (claviculae, scapulae) and anterior dorsal vertebrae and ribs. E Detail of right humerus. F Detail of posterior dorsal vertebrae and ribs, sacral vertebrae and ribs, and anterior caudal vertebrae and ribs. G Detail of left ilium and hindlimb. ar articular; as astragalus; bo basioccipital; cal calcaneus; cl clavicula; co coracoid; d dentary; en external naris; eo exoccipital; fe femur; fi fibula; fr frontal; hu humerus; il ilium; in internal naris; is ischium; j jugal; mx maxilla; na naris; o orbit; pa parietal; pl palatine; pmx premaxilla; pof postfrontal; po postorbital; prf prefrontal; pt pterygoid; pu pubis; q quadrate; qj quadratojugal; ti tibia; sacr sacral rib; sc scapula; so supraoccipital; sp splenial; sq squamosal; su surangular; utf upper temporal fenestra; v vomer

Fossil with teeth of Macroplacus raeticus from Triassic of Germany, on display at the Museo Civico di Storia Naturale di Milano

Pantydraco caducus, a sauropodomorph from the Late Triassic or Early Jurassic of England, after Yates, 2003, pencil drawing, digital coloring

Right hind limb of the sauropodomorph dinosaur Musankwa sanyatiensis gen. et sp. nov. (NHMZ 2521) from the Pebbly Arkose Formation (Norian, Upper Triassic) of Spurwing Island, Zimbabwe. A. Right femur in posterior (A1), lateral (A2), anterior (A3), medial (A4), proximal (A5), and distal (A6) views. B. Right tibia with conjoined astragalus in anterior (B1), lateral (B2), posterior (B3), medial (B4), and proximal (B5) views.

Left maxilla of the silesaurid Agnosphitys cromhallensis from the Late Triassic (Rhaetian) of England.

Life restoration of the Triassic ichthyosaur Callawayia neoscapularis. Three specimens of this ichthyosaur are known, the holotype, ROM 41993, and two referred specimens, TMP 94.380.11 and 94.382.2. The skull is primarily based on ROM 41993, cross-checked against TMP 94.380.11 and TMP 94.382.2. The vertebral column is based primarily on TMP 94.382.2 as it is the most complete of these specimens, while the ribs were based on ROM 41993. The forelimbs were mainly based on those of ROM 41993, with TMP 94.380.11 used to determine their breadth. The hindlimbs were based on TMP 94.380.11, especially the more complete right hindlimb. ROM 41993 was cross-scaled with TMP 94.380.11 by the dimensions of the forelimb epipodials, which produced similar vertebral dimensions. The two TMP specimens were cross-scaled based on femoral length, also producing similar vertebral dimensions. Nicholls & Manabe (2001) stated that no wedge-shaped caudal centra supporting a tailbend were found and that there was no evidence of a bend being present, though considered that they might have existed in the gap in the preserved caudals. Since various other Triassic ichthyosaurs have since been found to have tail bends, one was illustrated here. A modest downturn of roughly 15° was illustrated, comparable to that in Guanlingsaurus, and the location of the bend within the gap in the preserved vertebrae matches well with the location of the bend in Guizhouichthyosaurus. References McGowan, C. (1994). "A new species of Shastasaurus (Reptilia: Ichthyosauria) from the Triassic of British Columbia: The most complete exemplar of the genus". Journal of Vertebrate Paleontology 14 (2): 168–179. DOI:10.1080/02724634.1994.10011550. Nicholls, E. L.; Manabe, M. (2001). "A new genus of ichthyosaur from the Late Triassic Pardonet Formation of British Columbia: Bridging the Triassic-Jurassic gap". Canadian Journal of Earth Sciences 38 (6): 983–1002. Ji, C.; Jiang, D.Y.; Hao, W.; Sun, Y. (2011). "True tailbend occurred in the Late Triassic: Evidence from ichthyosaur skeletons of South China". Acta Scientiarum Naturalium Universitatis Pekinensis 47 (2): 309–314. Shang, Q. H.; Li, C. (2009). "On the occurrence of the ichthyosaur Shastasaurus in the Guanling biota (Late Triassic), Guizhou, China". Vertebrata PalAsiatica 47 (3): 178–193.

Nyasasaurus is a basal dinosauromorph that may be the earliest known dinosaur. It was a small bipedal animal at about 2-3 m in length. Nyasasaurus is difficult to classify due to inconclusive fossil evidence, but if it is a true dinosaur, it pushes the dinosaur lineage back about 12 million years to the Middle Triassic.

Fossil samples – e.g. ‘primitive’ bony fish (1, 2), a skull of a temnospondyl ‘amphibian’ (probably a metoposauroid) in dorsal view (3), a skull of an archosaur of the crocodile lineage (probably a phytosaur) in palatal view (4), holotype of the “gliding reptile” Icarosaurus siefkeri [1] (5) and Atreipus-Grallator-type dinosaur tracks (bottom right) – from the Newark Supergroup, i.e. a series of mainly Late Triassic to Early Jurassic sedimentary rocks of eastern North America ↑ Edwin H. Colbert: A gliding reptile from the Triassic of New Jersey. American Museum Novitates, 2230. American Museum of Natural History, New York 1966, digitallibrary.amnh.org, cf. fig. 3 therein.

Musango is a basal sauropodomorph dinosaur that lived during the Late Triassic period in what is now Zimbabwe. Typical of early sauropodomorphs, or "prosauropods," it was an obligate biped with a long neck, and a long tail for counterbalance. Musango grew to approximately 5 m in total body length.