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Avialae

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Avialans
Temporal range: Middle JurassicPresent, 150.8–0 Ma[1] Earliest 165 Ma if Anchiornithidae are members[2]
Fossil specimen of Jeholornis prima
Collage of four extant birds. Clockwise from top-left: Spanish imperial eagle (Aquila adalberti), common ostrich (Struthio camelus), mallard (Anas platyrhynchos), and common kingfisher (Alcedo atthis)
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: Saurischia
Clade: Theropoda
Clade: Pennaraptora
Clade: Paraves
Clade: Avialae
Gauthier, 1986
Subgroups

Avialae ("bird wings") is a clade containing the only living dinosaurs, the birds, and their closest relatives. It is usually defined as all theropod dinosaurs more closely related to birds (Aves) than to deinonychosaurs, though alternative definitions are occasionally used (see below).

Archaeopteryx lithographica, from the late Jurassic Period Solnhofen Formation of Germany, is usually considered the earliest known avialan which may have had the capability of powered flight;[3] a minority of studies have suggested that it might have been a deinonychosaur instead.[4] Several older (but non flight-capable) possible avialans are known from the late Jurassic Tiaojishan Formation of China, dated to about 160 million years ago.[5][6]

Definition

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Most researchers define Avialae as branch-based clade, though definitions vary. Many authors have used a definition similar to "all theropods closer to birds than to Deinonychus."[7][8] A nearly identical definition, "the theropod group that includes all taxa closer to Passer than to Dromaeosaurus", was used by Agnolín and Novas (2013) for their clade Averaptora, operating under the assumption that troodontids and birds were more closely related to each other than to dromaeosaurs. They also redefine Avialae as the smallest clade containing Archaeopteryx and modern birds.[9]

Additionally, beginning in the late 2000s and early 2010s, several groups of researchers began adding the genus Troodon as an additional specifier in the definition of Avialae. Troodon had long been considered a close relative of the dromaeosaurids in the larger group Deinonychosauria, though some contemporary studies found it and other troodontids more closely related to modern birds, and so it has been specifically excluded from Avialae in more recent studies.[10]

Avialae is also occasionally defined as an apomorphy-based clade (that is, one based on derived characteristics that were not present among lineage predecessors). Jacques Gauthier, who named Avialae in 1986, re-defined it in 2001 as all dinosaurs that possessed feathered wings used in flapping flight, and the birds that descended from them.[11][12]

Differentiation from Aves

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Gauthier and de Queiroz[12] (page 34) identified four conflicting ways of defining the term "Aves", which is a problem since the same biological name is being used four different ways. They proposed a solution, number 4 below, which is to reserve the term Aves only for the crown group, the last common ancestor of all living birds and all of its descendants. Other definitions of Aves found in literature were reassigned to other clade names.

  1. Aves can mean all reptiles closer to birds than to crocodiles (alternatively Avemetatarsalia [=Panaves])
  2. Aves can mean those advanced archosaurs with feathers (alternatively Avifilopluma)
  3. Aves can mean those feathered dinosaurs that can fly (alternately Avialae)
  4. Aves can mean the last common ancestor of all the currently living birds and all of its descendants (a "crown group"). (alternatively Neornithes)

Under the fourth definition Archaeopteryx is an avialan, and not a member of Aves. Gauthier's proposals have been adopted by many researchers in the field of paleontology and bird evolution, though the exact definitions applied have been inconsistent. Avialae, initially proposed to replace the traditional fossil content of Aves, is sometimes used synonymously with the vernacular term "bird" by these researchers.[10]

Evolution

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Avialae
Cladogram following the results of a phylogenetic study by Wang et al., 2016.[13]

The earliest known avialans come from the Tiaojishan Formation of China, which has been dated to the late Jurassic period (Oxfordian stage), about 160 million years ago.[10] The avialan species from this time period include Anchiornis huxleyi and Aurornis xui. Xiaotingia zhengi used to be considered a member, but was later classified within the clade Dromaeosauridae. The well-known Archaeopteryx dates from slightly later Jurassic rocks (about 155 million years old) from Germany. Many of these early avialans shared unusual anatomical features that may be ancestral to modern birds, but were later lost during bird evolution. These features include enlarged claws on the second toe which may have been held clear of the ground in life, and long feathers or "hind wings" covering the hind limbs and feet, which may have been used in aerial maneuvering.[14] It is also thought that early avialans were either cranially akinetic or had otherwise limited cranial kinesis.[15][16]

Avialans diversified into a wide variety of forms during the Cretaceous Period.[17] Many groups retained primitive characteristics, such as clawed wings and teeth, though the latter were lost independently in a number of avialan groups, including modern birds (Aves). While the earliest forms, such as Archaeopteryx and Shenzhouraptor, retained the long bony tails of their ancestors,[17] the tails of more advanced avialans were shortened with the advent of the pygostyle bone in the group Pygostylia. In the late Cretaceous, around 95 million years ago, the ancestor of all modern birds also evolved a better sense of smell.[18]

The following cladogram is based on the analysis by Hartman et al. (2019), which found flight likely evolved five separate times among paravian dinosaurs, two of those among Avialae (in Scansoriopterygids and other avialans). Archaeopteryx and "anchiornithids" were placed in Deinonychosauria, Avialae's sister group.[4]

In a study conducted in 2020, Archaeopteryx was recovered as an avialan.[19]

See also

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References

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  1. ^ Schweigert, G. (2007). "Ammonite biostratigraphy as a tool for dating Upper Jurassic lithographic limestones from South Germany – first results and open questions" (PDF). Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen. 245 (1): 117–125. doi:10.1127/0077-7749/2007/0245-0117. S2CID 140597349.
  2. ^ Zhang, H.; Wang, M.; Liu, X. (2008). "Constraints on the upper boundary age of the Tiaojishan Formation volcanic rocks in West Liaoning-North Hebei by LA-ICP-MS dating". Chinese Science Bulletin. 53 (22): 3574–3584. Bibcode:2008SciBu..53.3574Z. doi:10.1007/s11434-008-0287-4.
  3. ^ Alonso, P. D.; Milner, A. C.; Ketcham, R. A.; Cookson, M. J.; Rowe, T. B. (2004). "The avian nature of the brain and inner ear of Archaeopteryx" (PDF). Nature. 430 (7000): 666–669. Bibcode:2004Natur.430..666A. doi:10.1038/nature02706. PMID 15295597. S2CID 4391019. Archived from the original (PDF) on 2006-02-09. Supplementary info
  4. ^ a b Hartman, Scott; Mortimer, Mickey; Wahl, William R.; Lomax, Dean R.; Lippincott, Jessica; Lovelace, David M. (2019-07-10). "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. ISSN 2167-8359. PMC 6626525. PMID 31333906.
  5. ^ Hu, D.; Hou, L.; Zhang, L. & Xu, X. (2009). "A pre-Archaeopteryx troodontid theropod from China with long feathers on the metatarsus". Nature. 461 (7264): 640–643. Bibcode:2009Natur.461..640H. doi:10.1038/nature08322. PMID 19794491. S2CID 205218015.
  6. ^ Liu Y.-Q.; Kuang H.-W.; Jiang X.-J.; Peng N.; Xu H.; Sun H.-Y. (2012). "Timing of the earliest known feathered dinosaurs and transitional pterosaurs older than the Jehol Biota". Palaeogeography, Palaeoclimatology, Palaeoecology. 323–325: 1–12. Bibcode:2012PPP...323....1L. doi:10.1016/j.palaeo.2012.01.017.
  7. ^ Weishampel, David B.; Dodson, Peter; Osmólska, Halszka (eds.) (2004). The Dinosauria, Second Edition. University of California Press., 861 pp.
  8. ^ Senter, P (2007). "A new look at the phylogeny of Coelurosauria (Dinosauria: Theropoda)". Journal of Systematic Palaeontology. 5 (4): 429–463. Bibcode:2007JSPal...5..429S. doi:10.1017/S1477201907002143. S2CID 83726237.
  9. ^ Federico L. Agnolín & Fernando E. Novas (2013). Avian ancestors. A review of the phylogenetic relationships of the theropods Unenlagiidae, Microraptoria, Anchiornis and Scansoriopterygidae. SpringerBriefs in Earth System Sciences. pp. 1–96. doi:10.1007/978-94-007-5637-3. ISBN 978-94-007-5636-6. S2CID 199493087.
  10. ^ a b c Pascal Godefroit; Andrea Cau; Hu Dong-Yu; François Escuillié; Wu Wenhao; Gareth Dyke (2013). "A Jurassic avialan dinosaur from China resolves the early phylogenetic history of birds". Nature. 498 (7454): 359–62. Bibcode:2013Natur.498..359G. doi:10.1038/nature12168. PMID 23719374. S2CID 4364892.
  11. ^ Gauthier, J. (1986). "Saurischian monophyly and the origin of birds." In: K. Padian, ed. The origin of birds and the evolution of flight. San Francisco: California, Acad.Sci. pp.1–55. (Mem.Calif.Acad.Sci.8.)
  12. ^ a b Gauthier, J., and de Queiroz, K. (2001). "Feathered dinosaurs, flying dinosaurs, crown dinosaurs, and the name Aves." Pp. 7-41 in New perspectives on the origin and early evolution of birds: proceedings of the International Symposium in Honor of John H. Ostrom (J. A. Gauthier and L. F. Gall, eds.). Peabody Museum of Natural History, Yale University, New Haven, Connecticut, U.S.A.
  13. ^ Wang, M.; Wang, X.; Wang, Y.; Zhou, Z. (2016). "A new basal bird from China with implications for morphological diversity in early birds". Scientific Reports. 6: 19700. Bibcode:2016NatSR...619700W. doi:10.1038/srep19700. PMC 4726217. PMID 26806355.
  14. ^ Zheng, X.; Zhou, Z.; Wang, X.; Zhang, F.; Zhang, X.; Wang, Y.; Wei, G.; Wang, S.; Xu, X. (2013). "Hind Wings in Basal Birds and the Evolution of Leg Feathers". Science. 339 (6125): 1309–1312. Bibcode:2013Sci...339.1309Z. CiteSeerX 10.1.1.1031.5732. doi:10.1126/science.1228753. PMID 23493711. S2CID 206544531.
  15. ^ Wang, M.; Stidham, T.A.; Li, Z.; Xu, X.; Zhou, Z. (2021). "Cretaceous bird with dinosaur skull sheds light on avian cranial evolution". Nature Communications. 12 (1): 3890. Bibcode:2021NatCo..12.3890W. doi:10.1038/s41467-021-24147-z. PMC 8222284. PMID 34162868.
  16. ^ Hu, H.; Sansalone, G.; Wroe, S.; McDonald, P.G.; O'Connor, J.K.; Li, Z.; Xu, X; Zhou, Z. (2019). "Evolution of the vomer and its implications for cranial kinesis in Paraves". PNAS. 116 (39): 19571–19578. Bibcode:2019PNAS..11619571H. doi:10.1073/pnas.1907754116. PMC 6765239. PMID 31501339.
  17. ^ a b Chiappe, Luis M. (2007). Glorified Dinosaurs: The Origin and Early Evolution of Birds. Sydney: University of New South Wales Press. ISBN 978-0-86840-413-4.
  18. ^ Agency France-Presse (13 April 2011). "Birds survived dino extinction with keen senses". Cosmos Magazine. Archived from the original on 2 April 2015. Retrieved 11 June 2012.
  19. ^ Cau, Andrea (2020-02-25). "The body plan of Halszkaraptor escuilliei (Dinosauria, Theropoda) is not a transitional form along the evolution of dromaeosaurid hypercarnivory". PeerJ. 8: e8672. doi:10.7717/peerj.8672. ISSN 2167-8359. PMC 7047864. PMID 32140312.