Velociraptorinae

Velociraptorinae is a subfamily of the theropod group Dromaeosauridae. The earliest velociraptorines are probably Nuthetes from the United Kingdom, and possibly Deinonychus from North America. However, several indeterminate velociraptorines have also been discovered, dating to the Kimmeridgian stage, in the Late Jurassic Period. These fossils were discovered in the Langenberg quarry, Oker near Goslar, Germany.[1]

In 2007 paleontologists studied front limb bones of Velociraptor and discovered small bumps on the surface, known as quill knobs. The same feature is present in some bird bones, and represents the attachment point for strong secondary wing feathers. This finding provided the first direct evidence that velociraptorines, like all other maniraptorans, had feathers.[2]

While most velociraptorines were generally small animals, at least one species may have achieved gigantic sizes comparable to those found among the dromaeosaurines. So far, this unnamed giant velociraptorine is known only from isolated teeth found on the Isle of Wight, England. The teeth belong to an animal the size of dromaeosaurines of the genus Utahraptor, but they appear to belong to a velociraptorine, judging by the shape of the teeth and the anatomy of their serrations.[3]

Classification

Velociraptorine skeletons to scale

When erected by Barsbold in 1983, Velociraptorinae was conceived as a group containing Velociraptor and supposed closely related species. It was not until 1998 that this group was defined as a clade by Paul Sereno. Sereno defined the group as all dromaeosaurids more closely related to Dromaeosaurus than to Velociraptor. While several studies have since recovered a group of dromaeosaurids closely related to Velociraptor, they vary widely regarding which species are actually velociraptorines and which are either more basal or closer to Dromaeosaurus.

Novas and Pol (2005) found a distinct velociraptorine clade close to the traditional view, which included Velociraptor, Deinonychus, and material that was later named Tsaagan. A cladistic analysis conducted by Turner et al. (2012) also supported a traditional, monophyletic of Velociraptorinae.[4] However, some studies found a very different group of dromaeosaurids in velociraptorinae, such as Longrich and Currie (2009), which found Deinonychus to be a non-velociraptorine, non-dromaeosaurine eudromaeosaur, and Saurornitholestes to be a member of a more basal group they named Saurornitholestinae. A larger analysis in 2013 found some traditional velociraptorines, such as Tsaagan, to be more basal than Velociraptor, while others to be more closely related to Dromaeosaurus, making them dromaeosaurines. This study found Balaur, previously found to be a velociraptorine by most analyses, to be an avialan instead.[5]

The cladogram below follows a 2009 analysis by paleontologists Nicholas Longrich and Philip J. Currie, using a dataset of 114 characters scored for 23 taxa.[6]

Eudromaeosauria
Saurornitholestinae

Atrociraptor



Bambiraptor



Saurornitholestes





Deinonychus



Velociraptorinae
unnamed

Velociraptor



Itemirus



unnamed

Adasaurus



Tsaagan



Linheraptor




Dromaeosaurinae

Dromaeosaurus



Achillobator



Utahraptor






The cladogram below follows a 2012 analysis by Turner, Makovicky and Norell, using a dataset of 474 characters scored for 111 taxa.[4]

Eudromaeosauria

Dromaeosaurinae


Velociraptorinae

Bambiraptor




Tsaagan




Saurornitholestes




Adasaurus



Deinonychus



Velociraptor



Balaur







The cladogram below follows a 2013 analysis by Godefroit et al., using a dataset of 1,500 characters scored for 358 taxa.[5]

Eudromaeosauria

Tsaagan





Tianyuraptor



Bambiraptor





Velociraptor (=Velociraptorinae)


Dromaeosaurinae

Achillobator



Deinonychus



Saurornitholestes




Dromaeosaurus



Utahraptor







Distinguishing anatomical features

A diagnosis is a statement of the anatomical features of an organism (or group) that collectively distinguish it from all other organisms. The diagnosis of a taxonomic group of organisms includes the traits, known as synapomorphies, that are shared by two or more organisms in the group and are believed to have been present in their most recent common ancestor.

According to Currie (1995), Velociraptorinae can be distinguished based on the following characteristics:[7]

According to Turner et al. (2012), Velociraptorinae can be distinguished based on the following unambiguous characteristics:[4]

See also

References

  1. van der Lubbe, T., Richter, U. and Knotschke, N. (2009). "Velociraptorine dromaeosaurid teeth from the Kimmeridgian (Late Jurassic) of Germany." Acta Palaeontologica Polonica, 54(3): 401-408.
  2. Turner, A.H.; Makovicky, P.J.; Norell, M.A. (2007). "Feather quill knobs in the dinosaur Velociraptor". Science. 317 (5845): 1721. doi:10.1126/science.1145076. PMID 17885130.
  3. Naish, D. Hutt, and Martill, D.M. (2001). "Saurischian dinosaurs: theropods." in Martill, D.M. and Naish, D. (eds). Dinosaurs of the Isle of Wight. The Palaeontological Association, Field Guides to Fossils. 10, 242–309.
  4. 1 2 3 Turner, A. H.; Makovicky, P. J.; Norell, M. A. (2012). "A Review of Dromaeosaurid Systematics and Paravian Phylogeny". Bulletin of the American Museum of Natural History. 371: 1. doi:10.1206/748.1.
  5. 1 2 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.
  6. Longrich, N.R.; Currie, P.J. (2009). "A microraptorine (Dinosauria–Dromaeosauridae) from the Late Cretaceous of North America". PNAS. 106 (13): 5002–7. doi:10.1073/pnas.0811664106. PMC 2664043Freely accessible. PMID 19289829.
  7. Currie, P.J. 1995. New information on the anatomy and relationships of Dromaeosaurus albertensis (Dinosauria: Theropoda). Journal of Vertebrate Paleontology 15: 576–591.
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