Jump to content

Unenlagiinae: Difference between revisions

From Wikipedia, the free encyclopedia
[accepted revision][pending revision]
Content deleted Content added
Restored revision 1038158597 by Hemiauchenia (talk): LTA
No edit summary
Tags: Reverted Mobile edit Mobile web edit
Line 13: Line 13:
| subdivision = *{{extinct}}''[[Austroraptor]]''
| subdivision = *{{extinct}}''[[Austroraptor]]''
*{{extinct}}''[[Buitreraptor]]''
*{{extinct}}''[[Buitreraptor]]''
*{{extinct}}''[[Dakotaraptor]]''?
*{{extinct}}''[[Dakotaraptor]]''
*{{extinct}}''[[Neuquenraptor]]''
*{{extinct}}''[[Neuquenraptor]]''
*{{extinct}}''[[Pamparaptor]]''?
*{{extinct}}''[[Pamparaptor]]''
*{{extinct}}''[[Pyroraptor]]''?
*{{extinct}}''[[Pyroraptor]]''
*{{extinct}}''[[Rahonavis]]''?
*{{extinct}}''[[Unenlagia]]''
*{{extinct}}''[[Unenlagia]]''
*{{extinct}}''[[Unquillosaurus]]''?
*{{extinct}}''[[Unquillosaurus]]''
*{{extinct}}''[[Ypupiara]]''
*{{extinct}}''[[Ypupiara]]''
}}
}}

Revision as of 21:58, 10 August 2021

Unenlagiines
Temporal range: Late Cretaceous, 94–70 Ma Possible Early Cretaceous record
Skeletal mounts of two unenlagiines. From top left to right: Austroraptor and Buitreraptor.
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: Saurischia
Clade: Theropoda
Family: Dromaeosauridae
Subfamily: Unenlagiinae
Bonaparte, 1999
Type species
Unenlagia comahuensis
Novas & Puerta, 1997
Genera

Unenlagiinae is a subfamily of theropods. Unenlagiines are known from South America and Antarctica. With possible Unenlagiines being known from North America, Madagascar, Europe, and even Australia.

Description

Life restoration of Austroraptor

Most unenlagiines have been discovered in Argentina. The largest was Austroraptor, which measured up to 5–6 m (16.4–19.7 ft) in length, making it also one of the largest dromaeosaurids.[1] The subfamily is distinguished from other dromaeosaurids by a tail stiffened by lengthy chevrons and superior processes, a reduced second pedal ungual, a posteriorly oriented pubis and very elongated snouts. Unenlagiines also had elongated, slender hindlimbs with a subarctometatarsalian metatarsus, which is characterized by the pinched metatarsal III at the upper end. Their distinct anatomy from Laurasian dromaeosaurids was likely a consequence of the breakup of Pangaea into Gondwana and Laurasia, where the geological isolation of unenlagiines from their relatives resulted in allopatric speciation.[2][3]

Classification

During the description of Halszkaraptor in 2017, Cau et al. published a phylogenetic analysis of the Dromaeosauridae, in which, members of the Unenlagiinae are classified as:[4]

Unenlagiinae

In 2019, during the description of Hesperornithoides, many Paravian groups were examined for the inclusion of this new genus, including the Unenlagiinae. The analysis ended in the inclusion of Rahonavis, Pyroraptor and Dakotaraptor to the Unenlagiinae.[5]

Paleobiology

Metatarsus of Buitreraptor

A study performed by Gianechini and colleagues in 2020 indicates that unenlagiine dromaeosaurids of Gondwana possessed different hunting specializations than the eudromaeosaurs from Laurasia. The shorter second phalanx in the second digit of the foot of eudromaeosaurs allowed for increased force to be generated by that digit, which, combined with a shorter and wider metatarsus, and a noticeable marked hinge‐like morphology of the articular surfaces of metatarsals and phalanges, possibly allowed eudromaeosaurs to exert a greater gripping strength than unenlagiines, allowing for more efficient subduing and killing of large prey. In comparison, the unenlagiine dromaeosaurids possess a longer and slender subarctometatarsus, and less well‐marked hinge joints, a trait that possibly gave them greater cursorial capacities and allowed for greater speed than eudromaeosaurs. Additionally, the longer second phalanx of the second digit allowed unenlagiines fast movements of their feet's second digits to hunt smaller, faster types of prey. These differences in locomotor and predatory specializations may have been a key feature that influenced the evolutionary paths that shaped both groups of dromaeosaurs in the northern and southern hemispheres, respectively.[3]

See also

References

  1. ^ Novas, F. E.; Pol, D.; Canale, J. I.; Porfiri, J. D.; Calvo, J. O. (2008). "A bizarre Cretaceous theropod dinosaur from Patagonia and the evolution of Gondwanan dromaeosaurids". Proceedings of the Royal Society B: Biological Sciences. 276 (1659): 1101−1107. doi:10.1098/rspb.2008.1554. ISSN 1471-2954. PMC 2679073. PMID 19129109.
  2. ^ Gianechini, F. A. (2011). "Unenlagiinae revisited: dromaeosaurid theropods from South America". Anais da Academia Brasileira de Ciências. 83 (1): 163−195. doi:10.1590/s0001-37652011000100009. PMID 21437380.
  3. ^ a b Gianechini, F. A.; Ercoli, M. D.; Díaz-Martinez, I. (2020). "Differential locomotor and predatory strategies of Gondwanan and derived Laurasian dromaeosaurids (Dinosauria, Theropoda, Paraves): Inferences from morphometric and comparative anatomical studies". Journal of Anatomy. 236 (5): 772−797. doi:10.1111/joa.13153. PMC 7163733. PMID 32023660.{{cite journal}}: CS1 maint: PMC embargo expired (link)
  4. ^ Cau, A.; Beyrand, V.; Voeten, D. F. A. E.; Fernandez, V.; Tafforeau, P.; Stein, K.; Barsbold, R.; Tsogtbaatar, K.; Currie, P. J.; Godefroit, P. (2017). "Synchrotron scanning reveals amphibious ecomorphology in a new clade of bird-like dinosaurs". Nature. 552 (7685): 395−399. Bibcode:2017Natur.552..395C. doi:10.1038/nature24679. PMID 29211712. S2CID 4471941.
  5. ^ Hartman, S.; Mortimer, M.; Wahl, W. R.; Lomax, D. R.; Lippincott, J.; Lovelace, D. M. (2019). "A new paravian dinosaur from the Late Jurassic of North America supports a late acquisition of avian flight". PeerJ. 7: e7247. doi:10.7717/peerj.7247. PMC 6626525. PMID 31333906.