Maniraptoriformes: Difference between revisions
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{{Automatic taxobox |
{{Automatic taxobox |
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| name = Maniraptoriformes |
| name = Maniraptoriformes |
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| fossil_range = <br>[[Late Jurassic]]–[[Holocene|Present]], {{Fossil range| |
| fossil_range = <br>[[Late Jurassic]]–[[Holocene|Present]], {{Fossil range|167|0|earliest=196}}<small>Possible [[Early Jurassic]] record</small> |
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| image = Struthiomimus ROM.jpg |
| image = Struthiomimus ROM.jpg |
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|image_width = 250px |
|image_width = 250px |
Revision as of 10:48, 19 July 2016
Maniraptoriformes | |
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Ornithomimid (Struthiomimus altus) fossil cast | |
House sparrow (Passer domesticus) | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Dinosauria |
Clade: | Saurischia |
Clade: | Theropoda |
Clade: | Neocoelurosauria |
Clade: | Maniraptoriformes Holtz, 1995 |
Subgroups | |
| |
Synonyms | |
Maniraptoriformes is a clade of dinosaurs with pennaceous feathers and wings[2] that contains ornithomimosaurs and maniraptors. This group was named by Thomas Holtz, who defined it as "the most recent common ancestor of Ornithomimus and birds, and all descendants of that common ancestor."
Fossil evidence
Many fossils have been discovered in recent years, particularly in China. Many of the feathered dinosaurs belong to this clade. In particular, a fossil of the Alvarezsauridae Shuvuuia has a version of keratin consistent with that of avian feathers.[3]
Many nearly complete fossil maniraptoriforms are known from the late Jurassic. Archaeopteryx is known from Bavaria at 155-150 Ma. Ornitholestes, the troodontid WDC DML 110, Coelurus fragilis and Tanycolagreus topwilsoni are all known from the Morrison Formation in Wyoming at about 150 Ma. The Daohugou biota, including Anchiornis and Epidexipteryx, is the earliest record of maniraptoriformes, dating to about 160 Ma. One possible maniraptoriform, Eshanosaurus, lived even earlier, during the Early Jurassic, though its identification is controversial.[4]
The wide range of fossils in the early Cretaceous and morphological evidence suggests that the main branches of maniraptoriform differentiation were separate before the end of the Jurassic.
Until recently, the relatives of Tyrannosaurus were thought to be maniraptoriforms,[5] but this now seems unlikely.[6][7]
History of study
In 1994, a study by paleontologist Thomas Holtz found a close relationship between the Ornithomimosauria and Troodontidae, and named this group Bullatosauria. Holtz rejected this hypothesis in 1999, and most paleontologists now consider troodontids to be much more closely related to either birds or Dromaeosauridae than they are to ornithomimosaurs, causing the Bullatosauria to be abandoned. The name referred to the inflated (bulbous) sphenoid both groups shared. Holtz defined the group as the clade containing the most recent common ancestor of Troodon and Ornithomimus and all its descendants.[8] The concept is now considered redundant, and the clade Bullatosauria is now viewed as synonymous with Maniraptoriformes. In 2002, Gregory S. Paul named an apomorphy-based clade Avepectora, defined to include all theropods with a bird-like arrangement of the pectoral bones, where the angled shoulder girdle (coracoids) come in contact with the breastbone (sternum). According to Paul, ornithomimosaurs are the most basal members of this group.[9]
Classification
The relationships among coelurosaurs shown below were found in a phylogenetic analysis by Godefroit and colleagues in 2013.[10]
Maniraptoriformes | |
See also
References
- ^ Azuma, Y., Xu X., Shibata, M., Kawabe, S., Miyata, K., and Imai, T. 2016. "A bizarre theropod from the Early Cretaceous of Japan highlighting mosaic evolution among coelurosaurians." Scientific Reports, 6(20478). doi:10.1038/srep20478
- ^ Zelenitsky, D. K.; Therrien, F.; Erickson, G. M.; Debuhr, C. L.; Kobayashi, Y.; Eberth, D. A.; Hadfield, F. (2012). "Feathered Non-Avian Dinosaurs from North America Provide Insight into Wing Origins". Science. 338 (6106): 510–514. doi:10.1126/science.1225376. PMID 23112330.
- ^ Schweitzer, M.H.; Watt, J.A.; Avci, R.; Knapp, L.; Chiappe, L.; Norell, M.; Marshall, M. (1999). "Beta-keratin specific immunological reactivity in feather-like structures of the Cretaceous Alvarezsaurid, Shuvuuia deserti". Journal of Experimental Zoology. 285 (2): 146–157. doi:10.1002/(SICI)1097-010X(19990815)285:2<146::AID-JEZ7>3.0.CO;2-A. PMID 10440726.
- ^ Barrett, P.M. (2009). "The affinities of the enigmatic dinosaur Eshanosaurus deguchiianus from the Early Jurassic of Yunnan Province, People's Republic of China". Palaeontology. 52 (4): 681–688. doi:10.1111/j.1475-4983.2009.00887.x.
- ^ Benton, Michael J. (2004) Vertebrate Palaentology. 3rd ed. Wiley. ISBN 978-0-632-05637-8
- ^ Weishampel, David B., Dodson, Peter, and Osmólska, Halszka (2004) The Dinosauria. University of California Press. ISBN 0-520-25408-2
- ^ Senter, Phil (2007). "A new look at the phylogeny of coelurosauria (dinosauria: theropoda)". Journal of Systematic Palaeontology. 5 (4): 429. doi:10.1017/S1477201907002143.
- ^ Holtz, T.R. Jr (1994). "The phylogenetic position of the Tyrannosauridae. Implications for theropod systematics". Journal of Paleontology. 68: 1100–1117.
- ^ Paul, G.S. (2002). Dinosaurs of the Air: The Evolution and Loss of Flight in Dinosaurs and Birds. Baltimore: Johns Hopkins University Press. ISBN 0801867630.
- ^ Godefroit, Pascal; Cau, Andrea; Hu, Dong-Yu; Escuillié, François; Wu, Wenhao; Dyke, Gareth (2013). "A Jurassic avialan dinosaur from China resolves the early phylogenetic history of birds". Nature. 498 (7454): 359–362. Bibcode:2013Natur.498..359G. doi:10.1038/nature12168. PMID 23719374.