Coelurosauria is a subgroup of theropod dinosaurs that includescompsognathids,tyrannosauroids,ornithomimosaurs,maniraptorans, and over the recent years,megaraptorans (Although position within the clade is unclear).Maniraptora includesbirds, the only known dinosaur group alive today.[5] In the past, Coelurosauria was used to refer to all small theropods, but this classification has since been amended.
Mostfeathered dinosaurs discovered so far have been coelurosaurs.Philip J. Currie had considered it likely and probable that all coelurosaurs were feathered.[6] However, several skin impressions found for some members of this group show pebbly, scaly skin, indicating that feathers did not completely replace scales in all taxa.
The studying of anatomical traits in coelurosaurs indicates that the last common ancestor had evolved the ability to eat and digest plant matter, adapting to an omnivorous diet, an ability that could be a major contributor to the clade's success. Later groups would hold on to the omnivory, while others specialized in various directions, becoming insectivorous (Alvarezsauridae), herbivorous (Therizinosauridae) and carnivorous (Tyrannosauroidea andDromaeosauridae).[7] The group includes some of the largest (Tyrannosaurus) and smallest (Microraptor,Parvicursor) carnivorous dinosaurs ever discovered. Characteristics that distinguish coelurosaurs include:
asacrum (series of vertebrae that attach to the hips) longer than in other dinosaurs
Fossil evidence shows that the skin of even the most primitive coelurosaurs was covered primarily infeathers. Fossil traces of feathers, though rare, have been found in members of most major coelurosaurian lineages. Most coelurosaurs also retained scales and scutes on some portion of their bodies, particularly the feet, though some primitive coelurosaurian species are known to have had scales on the upper legs and portions of the tail as well. These includetyrannosauroids,Juravenator, andScansoriopteryx. Fossils of at least some of these animals (Scansoriopteryx and possiblyJuravenator) also preserve feathers elsewhere on the body.
Though once thought to be a feature exclusive to coelurosaurs, feathers or feather-like structures are also known in someornithischian dinosaurs (likeTianyulongandKulindadromeus), and inpterosaurs. Though it is unknown whether these are related to true feathers, recent analysis has suggested that the feather-like integument found in ornithischians may have evolved independently of coelurosaurs but this was estimated by assuming that primitive pterosaurs had scales.[8] In 2018, two anurognathid specimens were found to have integumentary structures similar to protofeathers. Based on phylogenetic analysis, protofeathers would have had a common origin withavemetatarsalians.[9][10]
Although rare, complete casts of theropodendocrania are known from fossils. Theropod endocrania can also be reconstructed from preserved braincases without damaging valuable specimens by using acomputed tomography scan and 3D reconstruction software. These finds are of evolutionary significance because they help document the emergence of the neurology of modern birds from that of earlier reptiles. An increase in the proportion of the brain occupied by the cerebrum seems to have occurred with the advent of the Coelurosauria and "continued throughout the evolution of maniraptorans and early birds."[11]
In the earlyCretaceous, a superb range of coelurosaurian fossils (including avians) are known from theYixian Formation in Liaoning. All known theropod dinosaurs from theYixian Formation are coelurosaurs. Many of the coelurosaurian lineages survived to the end of the Cretaceous period (about 66 Ma) and fossils of some lineages, such as theTyrannosauroidea, are best known from the late Cretaceous. A majority of coelurosaur groups became extinct in theCretaceous–Paleogene extinction event, including the Tyrannosauroidea,Ornithomimosauria,Oviraptorosauria,Deinonychosauria,Enantiornithes, andHesperornithes. Only theNeornithes, otherwise known as modern birds, survived, and continued to diversify after the extinction of the other dinosaurs into the numerous forms found today.
There is consensus among paleontologists that birds are descended from coelurosaurs. Under moderncladistical definitions, birds are considered the only living lineage of coelurosaurs. Birds are classified by most paleontologists as belonging to the subgroupManiraptora.[14]
A portion of a tail belonging to a juvenile coelurosaur was found in 2015, inside of a piece of amber.
Thephylogeny andtaxonomy of Coelurosauria has been subject to intensive research and revision. For many years, Coelurosauria was a 'dumping ground' for all small theropods. In the 1960s several distinctive lineages of coelurosaurs were recognized, and a number of new infraorders were erected, including theOrnithomimosauria,Deinonychosauria, andOviraptorosauria. During the 1980s and 1990s, paleontologists began to give Coelurosauria a formal definition, usually as all animals closer to birds than toAllosaurus, or equivalent specifiers. Under this modern definition, many small theropods are not classified as coelurosaurs at all, and some large theropods, such as thetyrannosaurids, were actually more advanced than allosaurs and therefore were reclassified as giant coelurosaurs. Even more drastically, thesegnosaurs, once not even regarded as theropods, have turned out to be non-carnivorous coelurosaurs related toTherizinosaurus. Senter (2007) listed 59 different published phylogenies since 1984. Those since 2005 have followed almost the same pattern, and differ significantly from many older phylogenies.
In 1994, a study bypaleontologistThomas Holtz found a close relationship between theOrnithomimosauria andTroodontidae, and named this groupBullatosauria. Holtz rejected this hypothesis in 1999, and most paleontologists now consider troodontids to be much more closely related to eitherbirds orDromaeosauridae 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 ofTroodon andOrnithomimus and all its descendants.[15] 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 cladeAvepectora, 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 mostbasal members of this group.[16] In 2010, Paul used Avepectora for a smaller clade, excluding ornithomimosaurs, compsognathids and alvarezsauroids.[17]
Within Coelurosauria exists a slightly less inclusiveclade namedTyrannoraptora. This clade was defined by Sereno (1999) as "Tyrannosaurus rex,Passer domesticus (the house sparrow), theirlast common ancestor, and all of its descendants".[18] As tyrannosauroids are considered to be the most basal large group within Coelurosauria, this means that the common ancestor of tyrannosauroids and birds was an even more basal coelurosaurian. As a result, almost all coelurosaurians are also tyrannoraptorans, with the only exceptions being particularly basal species such asZuolong salleei orSciurumimus albersdoerferi.
Several recently-named clades have been proposed to define the structure of Coelurosauria crownward of basal groups such as tyrannosauroids and compsognathids.Maniraptoromorpha, defined by Andrea Cau in 2018, includes all coelurosaurians more closely related to birds than to tyrannosauroids. Cau stated that the synapomorphies of the clade included "Keel or carinae in the postaxial cervical centra, absence of hyposphene-hypantra in caudal vertebrae (reversal to the plesiomorphic theropodan condition), a prominent dorsomedial process on the semilunate carpal, a convex ventral margin of the pubic foot, a subrectangular distal end of the tibia and a sulcus along the posterior margin of the proximal end of the fibula."[19] Another proposed clade isNeocoelurosauria, erected by Hendrickx, Mateus, Araújo and Choiniere (2019),[20] They define it as "the clade Compsognathidae + Maniraptoriformes", which can be more or less inclusive than Maniraptoromorpha depending on the topology.
The last, and most exclusive of these proposed subclades isManiraptoriformes. Maniraptoriformes is aclade which may have been united by the presence ofpennaceous feathers and wings.[21] This clade containsornithomimosaurs andmaniraptorans. The group was named byThomas Holtz, who defined it as "the most recent common ancestor ofOrnithomimus andbirds, and all descendants of that common ancestor." One of the possiblesynapomorphies of this clade is the presence of feathers homologous to those of birds, based on study of a specimen ofShuvuuia.[22]
The following family tree illustrates a synthesis of the relationships of the major coelurosaurian groups based on various studies conducted in the 2010s.[23]
^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.
^Barrett, P. M. (2009). "The affinities of the enigmatic dinosaurEshanosaurus deguchiianus from the Early Jurassic of Yunnan Province, People's Republic of China".Palaeontology.52 (4): 681−688.Bibcode:2009Palgy..52..681B.doi:10.1111/j.1475-4983.2009.00887.x.
^Turner, A.H., Makovicky, P.J., and Norell, M.A. 2012. A review of dromaeosaurid systematics and paravian phylogeny. Bulletin of the American Museum of Natural History 371: 1–206.
^Paul, G.S. (2002).Dinosaurs of the Air: The Evolution and Loss of Flight in Dinosaurs and Birds. Baltimore: Johns Hopkins University Press.ISBN0801867630.
^Paul, G. S. (2010). The Princeton field guide to dinosaurs Princeton University Press.Princeton, New Jersey.
^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.Bibcode:2012Sci...338..510Z.doi:10.1126/science.1225376.PMID23112330.
Larsson, H.C.E. (2001). "Endocranial anatomy ofCarcharodontosaurus saharicus (Theropoda: Allosauroidea) and its implications for theropod brain evolution". In Tanke, D. H.; Carpenter, K.; Skrepnick, M. W. (eds.).Mesozoic Vertebrate Life. Indiana University Press. pp. 19–33.
Mayr, G., B. Pohl & D.S. Peters (2005). "A well-preservedArchaeopteryx specimen with theropod features".Science,310(5753): 1483–1486.
Padian, K (2004). "Basal Avialae". In Weishampel, D.B.; Dodson, P.; Osmólska, H. (eds.).The Dinosauria (2nd ed.). Berkeley: University of California Press. pp. 210–231.ISBN0-520-24209-2.
Senter, P. (2007). "A new look at the phylogeny of Coelurosauria (Dinosauria: Theropoda)."Journal of Systematic Palaeontology, (doi:10.1017/S1477201907002143).
Zanno, L.E., Gillette, D.D., Albright, L.B., and Titus, A.L. (2009). "A new North American therizinosaurid and the role of herbivory in 'predatory' dinosaur evolution."Proceedings of the Royal Society B, Published online before print July 15, 2009,doi:10.1098/rspb.2009.1029.