Sarcosaurus

Sarcosaurus (meaning "flesh lizard") is a genus of theropod dinosaur, roughly 3.5 metres (11 ft) long. It lived during the Hettangian-Sinemurian boundary of the Early Jurassic, about 199-194 million years ago. Sarcosaurus is one of the earliest known Jurassic theropods, and one of only a handful of theropod genera from this time period. Along with Dracoraptor hanigani it is one of the two described neotheropods from the lowermost Jurassic of the United Kingdom.[1]

Sarcosaurus
Temporal range: Hettangian-Sinemurian, 199–194 Ma
Skeletons of the known specimens of Sarcosaurus woodi
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: Saurischia
Clade: Theropoda
Clade: Neotheropoda
Genus: Sarcosaurus
Andrews, 1921
Type species
Sarcosaurus woodi
Andrews, 1921
Synonyms

Description

Pelvis and parts of femur and dorsal vertebra

The holotype is NHMUK PV R4840 that includes a posterior dorsal vertebra, partial left and right ilia, that are fused to the proximal portion of the pubis, lacking the femoral head. The specimen shows some evidence of skeletal maturity, meaning it is not an early juvenile, but its exact ontogenetic stage cannot be ascertained.[1] Referred specimens include the non mature NHMUK PV R3542 (holotype of Sarcosaurus andrewsi) that includes a complete right tibia; WARMS G667–690, a partial skeleton of a single individual that includes posterior dorsal vertebra, middle caudal vertebra, dorsal rib fragments, left ilium, right and left pubes, femora and tibiae, proximal end of left fibula, probable distal half of fibula, distal portions of metatarsals IV, II or III proximal half of left pedal phalanx II-1, and three indeterminate bone fragments.[1][2] Sarcosaurus shares certain morphological conditions with other neotheropods, including Liliensternus liliensterni (collateral fossae of the metatarsal II with similar development and shape on both sides, larger ratio on the centrum) and Dilophosaurus wetherilli (lateral collateral fossa is bigger than the medial one in the metatarsal, middle caudal series proportionately lower and narrower than the middle−posterior dorsal vertebra). Sarcosaurus was a bipedal predator, probably able to run fast and catch small prey. The holotype belonged to a 3.5 m long animal whose weight was no greater than 50-60 kg. NHMUK PV R3542 belonged to a larger animal, estimated to have had a maximum length of 5 m and a weight of 140 kg.[3]

History of discovery

The fossils of Sarcosaurus were found in the Lower Lias of England. The type species, Sarcosaurus woodi, was first described by Charles William Andrews in 1921 shortly after a partial skeleton had been found by S.L. Wood near Barrow-on-Soar. The generic name is derived from Greek sarx, "flesh". The specific name honours Wood. The holotype, BMNH 4840/1, consists of a pelvis, a vertebra and the upper part of a femur. The preserved length of the femur is 31.5 centimetres (12.4 in).[4] A second species, Sarcosaurus andrewsi, was named by Friedrich von Huene in 1932,[5] based on a 445 millimetres (17.5 in) tibia, BMNH R3542, described by Arthur Smith Woodward in 1908 and found near Wilmcote.[6] Confusingly von Huene in the same publication named the very same fossil Magnosaurus woodwardi. Later he made a choice for S. andrewsi to be the valid name.[7] In 1974 S. andrewsi was reclassified as Megalosaurus andrewsi by Michael Waldman, on the probably erroneous assumption it was a megalosaurid.[8] A later study concluded the two species to be indistinguishable except for size, but other authors consider any identity to be unprovable as there are no comparable remains and conclude both species to lack autapomorphies and therefore to be nomina dubia.[9] Von Huene in 1932 referred a partial skeleton from the collection of the Warwick Museum to S. woodi but the identity is unproven; in 1995 it was given the generic name "Liassaurus"[10] but this has remained a nomen nudum. The specimen is likely one individual, located in the same stratiagraphic position as the holotypic specimen. Unfortunately, there are few available overlapping elements from the specimen and the Holotype. Both specimens preserve a relatively complete femur: however, the features of both (an anteromedially directed head, a relatively long fourth trochanter and a trochanteric shelf) are plesiomorphic and thus do not indicate conspecifity or clade membership. It is noted, however, that there are no features which are present in one specimen but not the other.

Phylogeny

Andrews originally assigned Sarcosaurus to the Megalosauridae. The first to suggest a more basal position was Samuel Paul Welles who placed it in the Coelophysidae.[11] Later analyses resulted in either a position in the Ceratosauria,[12] or in the Coelophysoidea.[13] Ezcurra (2012) found Sarcosaurus to be the most basal ceratosaur in a large unpublished analysis.[14]. In 2018, Andrea Cau in the large analysis of Saltriovenator found Sarcosaurus to be a dilophosaurid with good amount of support in the data.[15] In 2020, Ezcurra et al. recovered Sarcosaurus as a close relative of Averostra due to the presence of shared characters including an anteroventrally oriented ventral margin of the preacetabular process in lateral view on the illium and a femur with a poorly posteriorly developed fourth trochanter. Their cladogram is shown below:[1]

Theropoda 

Tawa

Chindesaurus

Eodromaeus

Neotheropoda

Coelophysoidea

Zupaysaurus

Gojirasaurus

Cryolophosaurus

Dilophosaurus

Sarcosaurus

Tachiraptor

Averostra

Palaeoenvironment

Holotype specimen was collected from strata (bucklandi zone, Sinemurian) that were deposited in epicontinental, shallow, marine settings affected by sea-level fluctuations and a warm, predominantly humid climate.[16] In south-western Warwickshire is represented by the upper part of the Rugby Limestone Member (Hettangian-Sinemurian) of the Blue Lias Formation . with typhical lithofacies of alternating mudrocks and generally fine-grained and frequently highly fossiliferous limestones.[17] the Rugby Limestone Member was deposited at a palaeolatitude of approximately 35° N in a storm-influenced offshore setting.[18] Wilmcote was related to the eastern margin of the Worcester Graben during the Early Jurassic and adjacent to the East Midlands Shelf.[19] The western margin of the emergent London Platform at 60−80 km to the south-east was probably the principal source of terrestrial biodebris.[20]

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See also

References

  1. Ezcurra, M. D.; Butler, R. J.; Maidment, S. C. R.; Sansom, I. J.; Meade, L. E.; Radley, J. D. (2020). "A revision of the early neotheropod genus Sarcosaurus from the Early Jurassic (Hettangian–Sinemurian) of central England". Zoological Journal of the Linnean Society. doi:10.1093/zoolinnean/zlaa054.
  2. Carrano and Sampson (2004). "A review of coelophysoids (Dinosauria: Theropoda) from the Early Jurassic of Europe, with comments on the late history of the Coelophysoidea." N. Jb. Geol. Palaont. Mh., 2004(9): 537-558.
  3. Molina-Pérez, R., Larramendi, A., Connolly, D., & Cruz, G. Á. R. (2019). Dinosaur Facts and Figures: The Theropods and Other Dinosauriformes. Princeton University Press.
  4. Andrews, C.W., 1921, "On some remains of a theropodous dinosaur from the Lower Lias of Barrow-on-Soar", Annals and Magazine of Natural History, series 9 8: 570-576
  5. von Huene, F., 1932, Die fossile Reptil-Ordnung Saurischia, ihre Entwicklung und Geschichte, Monographien zur Geologie und Palaeontologie 1(4) pp. 361
  6. Woodward, A.S. 1908. "Note on a megalosaurian tibia from the Lower Lias of Wilmcote, Warwickshire". Annals and Magazine of Natural History. 8(1): 257-259
  7. Huene, F. von, 1956, Paläontologie und Phylogenie der niederen Tetrapoden. Gustav Fischer Verlag, Jena. 716 pp
  8. Waldman, M. 1974. "Megalosaurids from the Bajocian (Middle Jurassic) of Dorset". Paleontology 17(2): 325-339
  9. D. Naish and D. M. Martill. 2007. "Dinosaurs of Great Britain and the role of the Geological Society of London in their discovery: basal Dinosauria and Saurischia". Journal of the Geological Society, London 164: 493-510
  10. Pickering, S. 1995. Jurassic Park: Unauthorized Jewish Fractals in Philopatry. A Fractal Scaling in Dinosaurology Project, 2nd revised printing. Capitola, California. 478 pp
  11. S.P. Welles. 1984. "Dilophosaurus wetherilli (Dinosauria, Theropoda): osteology and comparisons". Palaeontographica Abteilung A 185: 85-180
  12. J A. Gauthier. 1986. "Saurischian monophyly and the origin of birds". In: The Origin of Birds and the Evolution of Flight, K. Padian (ed.), Memoirs of the California Academy of Sciences 8: 1-55
  13. M.T. Carrano, J.R. Hutchinson, and S.D. Sampson. 2005. "New information on Segisaurus halli, a small theropod dinosaur from the Early Jurassic of Arizona". Journal of Vertebrate Paleontology 25 (4): 835-849
  14. Ezcurra, 2012. Phylogenetic analysis of Late Triassic - Early Jurassic neotheropod dinosaurs: Implications for the early theropod radiation. Journal of Vertebrate Paleontology. Program and Abstracts 2012, 91.
  15. Dal Sasso C, Maganuco S, Cau A. 2018. The oldest ceratosaurian (Dinosauria: Theropoda), from the Lower Jurassic of Italy, sheds light on the evolution of the three-fingered hand of birds. PeerJ 6:e5976
  16. Hesselbo SP. 2008. Sequence stratigraphy and inferred relative sea-level change from the onshore British Jurassic.Proceedings of the Geologists’ Association 119: 19−34
  17. Ambrose K. 2001. The lithostratigraphy of the Blue Lias Formation (Late Rhaetian–Early Sinemurian) in the southern part of the English Midlands. Proceedings of the Geologists’ Association 112: 97−110
  18. Weedon GP, Jenkyns HC, Page KN. 2017. Combined sealevel and climatic control on limestone formation, hiatuses and ammonite preservation in the Blue Lias Formation, South Britain (uppermost Triassic–Lower Jurassic). Geological Magazine 155: 1117−1149.
  19. Radley JD. 2003. Warwickshire’s Jurassic geology, past,present and future. Mercian Geologist 15: 209−218
  20. Cox BM, SumblerMG, Ivimey-Cook HC. 1999. "A formational framework for the Lower Jurassic of England and Wales (onshore area)". British Geological Survey Research Report RR/99/01: 1–28.
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