Biology:Overoraptor

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Short description: Extinct genus of theropod dinosaurs

Overoraptor
Temporal range: Late Cretaceous,
Cenomanian–Turonian
↓
Overoraptor chimentoi.png
Life restoration
Scientific classification e
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: Saurischia
Clade: Theropoda
Clade: Maniraptora
Clade: Pennaraptora
Clade: Paraves
Genus: †Overoraptor
Type species
† Overoraptor chimentoi
Motta et al., 2020

Overoraptor (/ˌʊuvərʊuˈræptər/, meaning "piebald thief") is an extinct genus of paravian theropod of uncertain affinities from the Late Cretaceous Huincul Formation of Argentinian Patagonia. The genus contains a single species, O. chimentoi, known from several bones of the hands, feet, and hips alongside some vertebrae.

Discovery and naming

Overoraptor is located in Argentina
Overoraptor
class=notpageimage|
Overoraptor type locality in Rio Negro Province, Argentina

The fossil specimens of Overoraptor were unearthed by Dr. Roberto Nicolás Chimento in the Violante Farm locality, which is southeast of the Ezequiel Ramos-Mexía lake, in the northwestern portion of Rio Negro Province, Argentina. This outcrop is part of the Huincul Formation, which is dated to the Cenomanian-Turonian boundary in the Cretaceous period. This formation has yielded some of the largest South American dinosaurs including the massive sauropod Argentinosaurus and the theropod Mapusaurus.[1]

The precise date of the discovery of the type series of Overoraptor is not publicly known, but the specimens were reposited in the collections of the Carlos Ameghino Provincial Museum in Cipolletti, which is near the outcrop of the Huincul Formation where the specimens were discovered. The fossils were described as a new genus and species of paravian theropod in May 2020 by Matías Motta, Federico Agnolín, Federico Brissón Egli, and Fernando Novas in the journal The Science of Nature (or Naturwissenschaften).[1]

The holotype specimen, MACN-Pv 805, was disarticulated when it was found and it is relatively fragmentary. It consists of two phalanges and a metacarpal of the right hand, two hemal arches, the right scapula, the right ulna, a partial ilium, a partial pubis, two metatarsals from each foot, and several phalanges and unguals from the left foot.[1]

The paratype specimen, MPCA-Pv 818, was discovered at the same locality in association with the holotype. It is about 20% smaller than the holotype, which led the researchers describing it to conclude that they were likely not from a fully-grown animal. The paratype consists of two phalanges from the right hand, a fragment of the ilium, the right pubis, one of the right metatarsals, and one pedal phalanx from each foot.[1]

The generic name, Overoraptor, comes from the Spanish word "overo", meaning "piebald"—referencing the coloration of the fossils—and the Latin word "raptor", meaning "thief". The specific epithet, "chimentoi", was given in honor of Roberto Nicolás Chimento, who initially discovered its remains.[1]

Description

In their 2020 description of the genus, Motta and colleagues estimated that Overoraptor would have been about 1.3 metres (4.3 ft) in length, although they do not provide an estimate of the animal's mass. They diagnosed Overoraptor as being distinct from all other paravians from the following unique autapomorphies: a medial deflection at the distal end of the scapula, a reduced and ridge-like acromial process, an extensive crest on metacarpal I, a crest ending in a distal posterior tubicle on metatarsal II, and a metatarsal III that is taller than it is wide at the midpoint along its length. Motta and colleagues further diagnosed the genus by the co-occurrence of the following autapomorphies: lateral ridges on the caudal centra, a robust ulna, a saddle-shaped radial cotyle on the ulna, a non-hinged joint at the distal end of metatarsal III, and dorsally displaced pits on the second toe. In the description of its osteology, Motta and colleagues considered both the holotype and paratype together, rather than describing each specimen individually.[1]

The scapular anatomy of Overoraptor resembles that of stem-avialans in the presence of a cup-shaped glenoid fossa, but it differs from most other paravians in that the acromial process projects dorsally rather than medially. The overall morphology of the scapula resembles the enigmatic paravian taxon Rahonavis because the scapular blade projects medially outward at its distal-most end. The ratio of the lengths of the ulna to the metacarpals is similar to the ratio found in dromaeosaurs and less than that of more derived avialans. The ulna itself is also curved, which is the plesiomorphic condition in paravians, unlike the straight ulnae of Anchiornis and related taxa. However, the ulna of Overoraptor resembles the derived avialan condition in the presence of a saddle-shaped cotyle on the ulnar-radial articular surface.[1]

The metacarpal bones of Overoraptor were noted by Motta and colleagues to be unusual in shape, namely that it is proportionally much wider and shorter than those known from other non-avialan paravians and there is a distinctly asymmetrical ginglymoidal surface which articulates with the lateral condyle. The manual phalanges are slender and elongate, which is common in the paravian taxa that retain their fingers. Similarly, the manual unguals are mediolaterally compressed, sharp, and curved, similar to the condition seen in dromaeosaurs.[1]

The foot bones of Overoraptor are sub-arctometatarsalian, meaning the middle metatarsal narrows at the medial end but it is not completely pinched together by the other two bones of the ankle. The foot also bears the archetypal raptorial second digit (the characteristic toe claw of dromaeosaurs), which is short in length and proportionally robust relative to other taxa with this claw.[1]

Classification

In order to evaluate the phylogenetic position of Overoraptor within paraves, Motta and colleagues employed the data sets used by Agnolin and Novas (2013), Brusatte and colleagues (2014), Gianechini and colleagues (2017), and Hu and colleagues (2018) and added the scored characters of the new taxon. They also modified these data sets to include data found in more recently published research for some taxa.[1]

Their analyses recovered Overoraptor in a variety of positions including as a basal maniraptoran, a basal pennaraptoran, and a basal paravian, but they found the tree with the highest support values in their analysis recovered Overoraptor as the sister taxon of Rahonavis in a clade that is the sister-taxon of avialae and to which unenlagiidae is basal. The Overoraptor-Rahonavis clade was recovered with the following synapomorphies: a complex set of ridges on the lateral surfaces of the caudal centra and a medial deflection of the distal end of the scapular blade. Even considering the similarities between the two taxa, Motta and colleagues also remark that the recovery of this clade may be the result of the unique mix of plesiomorphic and derived characters present in Overoraptor. The recovery of this clade is also suggested to be an early indicator of a much more diverse community of paravians across Gondwana that have yet to be fully uncovered.[1]

A number of unorthodox results were obtained from the analysis of Motta and colleagues. They recovered microraptorians and unenlagiines as being outside of dromaeosauridae as successive stem clades to avialae. They similarly found troodontids as being the sister group of all other paravians rather than being either the sister group of dromaeosaurs or avialans,[1] which have been the results obtained by other recent analyses.[2][3][4][5][6] An abbreviated version of the strict consensus tree from their analysis using the data set from Agnolin and Novas (2013) is shown below.[1]

Paraves
  Troodontidae
Latenivenatrix (white background).png
 
 
 

Dromaeosauridae Dromaeosaurus Restoration.png

 
 
 

Microraptoria Microraptor Restoration (cropped).png

 
 
 

Unenlagiidae Austroraptor Restoration.png

 
 
 
 

Overoraptor Overoraptor chimentoi.png

 
 

Rahonavis Rahonavis NT.jpg

 
 
Avialae
 
 

Alcmonavis

 
  Archaeopterygidae
Archaeopteryx.png
 
 
 
  Anchiornithidae
Anchiornis.png
 
 
 

Jeholornithidae Jeholornis mmartyniuk wiki.jpg

 
  Pygostylia
Meyers grosses Konversations-Lexikon - ein Nachschlagewerk des allgemeinen Wissens (1908) (Antwerpener Breiftaube).jpg
 
 
 
 
 
 
 
 
 

In 2021, Andrea Cau and Daniel Madzia published their redescription of the troodontid Borogovia, which contained a phylogenetic analysis using a wide variety of coelurosaur taxa. They used several different interpretive frameworks including the coding of Rahonavis as an unenlagiine, Balaur as a velociraptorine, and halszkaraptorines as being basal to the troodontid-dromaeosaurid split as well as an unweighted analysis without these constraints. The poorly-understood taxon Fukuivenator was also coded as a paravian,[7] although recent studies have resolved that it is probably a basal therizinosaur[8] or some other non-paravian maniraptoran.[3] The most strongly-supported result of their analysis was one in which troodontidae was the sister taxon of avialae, which includes Overoraptor, Rahonavis, Balaur, and several other taxa. An abbreviated version of the tree recovered by their parsimony analysis can be seen below.[7]

Paraves
 

Fukuivenator Fukuivenator (Therizinosauria).png

 
 
 

Dromaeosauridae Dromaeosaurus Restoration.png

 
 
  Troodontidae
Latenivenatrix (white background).png
 
Avialae
 
  Archaeopteryx
Archaeopteryx.png
 
  Anchiornithidae
Anchiornis.png
 
 
 
 

"Archaeopteryx" albersdoerferi

 
 
 

Alcmonavis

 
 

Rahonavis Rahonavis NT.jpg

 
 
 

Overoraptor Overoraptor chimentoi.png

 
 
  Balaur
Balaur by Mark P. Witton.png
 
 

Jeholornithiformes Jeholornis mmartyniuk wiki.jpg

 
  Pygostylia
Meyers grosses Konversations-Lexikon - ein Nachschlagewerk des allgemeinen Wissens (1908) (Antwerpener Breiftaube).jpg
 
 
 
 
 
 
 

Paleoecology

Paleoenvironment

Overoraptor was discovered in the Argentine Province of Neuquén. It was originally reported from the Huincul Group of the Río Limay Formation,[9] which have since become known as the Huincul Formation and the Río Limay Subgroup, the latter of which is a subdivision of the Neuquén Group. This unit is located in the Neuquén Basin in Patagonia. The Huincul Formation is composed of yellowish and greenish sandstones of fine-to-medium grain, some of which are tuffaceous.[10] These deposits were laid down during the Upper Cretaceous, either in the middle Cenomanian to early Turonian stages[11] or the early Turonian to late Santonian.[12] The deposits represent the drainage system of a braided river.[13]

The Huincul Formation is thought to represent an arid environment with ephemeral or seasonal streams.[14] In some areas, it is up to 250 metres (820 ft) thick. It is mainly composed of green and yellow sandstones and can easily be differentiated from the overlying Lisandro Formation, which is red in color. The Candeleros Formation, underlying the Huincul, is composed of darker sediments, making all three formations easily distinguishable.[15][16]

Fossilised pollen indicates a wide variety of plants were present in the Huincul Formation. A study of the El Zampal section of the formation found hornworts, liverworts, ferns, conifers, and some angiosperms (flowering plants).[17]

Contemporary fauna

Size comparison of some of the fauna of the Huincul Formation, with Overoraptor shown in red

The Huincul Formation is among the richest Patagonian vertebrate associations, preserving fish including lungfish and gar, chelid turtles, squamates, sphenodonts, neosuchian crocodilians, and a wide variety of dinosaurs.[11][18] Vertebrates are most commonly found in the lower, and therefore older, part of the formation.[19]

The Violante Farm locality is one of the most productive in the Huincul Formation, having yielded specimens of a wide variety of non-avian dinosaur species. Among these were the abelisaur Tralkasaurus, the megaraptoran Aoniraptor, the carcharodontosaur Taurovenator, and the enigmatic taxon Gualicho in addition to a variety of remains from indeterminate abelisaurs and coelurosaurs. Specimens of the titanosaur Choconsaurus were also discovered at this locality and represent the largest animal confidently known to have coexisted at this locality.[20]

Many other non-avian dinosaurs are known from the Huincul Formation, although it is not known with confidence if all of them coexisted with Overoraptor.[21] Sauropods are represented by the giant titanosaurs Bustingorrytitan, Chucarosaurus, and Argentinosaurus as well as the rebbachisaurids Cathartesaura, Limaysaurus, and Sidersaura.[22][23] Theropods are also diverse and include the abelisaurs Ilokelesia and Skorpiovenator, the noasaurid Huinculsaurus, the carcharodontosaurids Mapusaurus and Meraxes.[24]

See also

References

  1. ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 Matías J. Motta; Federico L. Agnolín; Federico Brissón Egli; Fernando E. Novas (2020). "New theropod dinosaur from the Upper Cretaceous of Patagonia sheds light on the paravian radiation in Gondwana". The Science of Nature 107 (3): Article number 24. doi:10.1007/s00114-020-01682-1. PMID 32468191. Bibcode: 2020SciNa.107...24M. 
  2. ↑ Napoli, J. G.; Ruebenstahl, A. A.; Bhullar, B.-A. S.; Turner, A. H.; Norell, M. A. (2021). "A New Dromaeosaurid (Dinosauria: Coelurosauria) from Khulsan, Central Mongolia". American Museum Novitates (3982): 1–47. doi:10.1206/3982.1. ISSN 0003-0082. https://digitallibrary.amnh.org/bitstream/handle/2246/7286/3982.pdf?sequence=1&isAllowed=y. 
  3. ↑ 3.0 3.1 Wang, Xuri; Cau, Andrea; Wang, Zhengdong; Yu, Kaifeng; Wu, Wenhao; Wang, Yang; Liu, Yichuan (2023-06-05). "A new theropod dinosaur from the Lower Cretaceous Longjiang Formation of Inner Mongolia (China)" (in en). Cretaceous Research 151: 105605. doi:10.1016/j.cretres.2023.105605. ISSN 0195-6671. 
  4. ↑ Wang, Xuri; Cau, Andrea; Guo, Bin; Ma, Feimin; Qing, Gele; Liu, Yichuan (2022-11-19). "Intestinal preservation in a birdlike dinosaur supports conservatism in digestive canal evolution among theropods" (in en). Scientific Reports 12 (1): 19965. doi:10.1038/s41598-022-24602-x. ISSN 2045-2322. PMID 36402874. 
  5. ↑ Pei, R.; Qin, Yuying; Wen, Aishu; Zhao, Q.; Wang, Z.; Liu, Z.; Guo, W.; Liu, P. et al. (2022). "A New Troodontid from the Upper Cretaceous Gobi Basin of Inner Mongolia, China". Cretaceous Research 130: Article 105052. doi:10.1016/j.cretres.2021.105052. 
  6. ↑ Turner, Alan H.; Montanari, Shaena; Norell, Mark A. (2021). "A New Dromaeosaurid from the Late Cretaceous Khulsan Locality of Mongolia". American Museum Novitates (3965): 1–48. doi:10.1206/3965.1. ISSN 0003-0082. http://digitallibrary.amnh.org/bitstream/handle/2246/7251/N3965.pdf?sequence=1&isAllowed=y. 
  7. ↑ 7.0 7.1 "The phylogenetic affinities and morphological peculiarities of the bird-like dinosaur Borogovia gracilicrus from the Upper Cretaceous of Mongolia". PeerJ 9: e12640. 2021. doi:10.7717/peerj.12640. PMID 34963824. 
  8. ↑ Hattori, S.; Kawabe, S.; Imai, T.; Shibata, M.; Miyata, K.; Xu, X.; Azuma, Y. (2021). "Osteology of Fukuiraptor paradoxus: A bizarre maniraptoran theropod from the Early Cretaceous of Fukui, Japan". Memoir of the Fukui Prefectural Dinosaur Museum 20: 1–82. https://www.dinosaur.pref.fukui.jp/archive/memoir/memoir020-001.pdf. 
  9. ↑ Bonaparte, J.; Coria, R. (1993). "Un nuevo y gigantesco sauropodo titanosaurio de la Formacion Rio Limay (Albiano-Cenomaniano) de la Provincia del Neuquen, Argentina" (in es). Ameghiniana 30 (3): 271–282. 
  10. ↑ Leanza, H.A; Apesteguı́a, S.; Novas, F.E; de la Fuente, M.S. (February 1, 2004). "Cretaceous terrestrial beds from the Neuquén Basin (Argentina) and their tetrapod assemblages". Cretaceous Research 25 (1): 61–87. doi:10.1016/j.cretres.2003.10.005. ISSN 0195-6671. Bibcode: 2004CrRes..25...61L. 
  11. ↑ 11.0 11.1 Motta, M.J.; Aranciaga Rolando, A.M.; Rozadilla, S.; Agnolín, F.E.; Chimento, N.R.; Egli, F.B.; Novas, F.E. (2016). "New theropod fauna from the upper cretaceous (Huincul Formation) of Northwestern Patagonia, Argentina". New Mexico Museum of Natural History and Science Bulletin 71: 231–253. https://books.google.com/books?id=OsJQDwAAQBAJ&q=huincul+formation+Argentinosaurus&pg=PA231. 
  12. ↑ Corbella, H.; Novas, F.E.; Apesteguía, S.; Leanza, H. (2004). "First fission-track age for the dinosaur-bearing Neuquén Group (Upper Cretaceous), Neuquén Basin, Argentina". Revista del Museo Argentino de Ciencias Naturales. Nueva Serie 6 (21): 227=232. doi:10.22179/REVMACN.6.84. http://revista.macn.gob.ar/ojs/index.php/RevMus/article/viewFile/84/77. 
  13. ↑ Rainoldi, A.L.; Franchini, Marta; Beaufort, D.; Mozley, P.; Giusiano, A.; Nora, C.; Patrier, P.; Impiccini, A. et al. (2015). "Mineral reactions associated with hydrocarbon paleomigration in the Huincul High, Neuquén Basin, Argentina". GSA Bulletin 127 (11–12): 1711–1729. doi:10.1130/B31201.1. Bibcode: 2015GSAB..127.1711R. https://www.researchgate.net/publication/277929681. 
  14. ↑ Coria, R.A.; Currie, P.J. (2006). "A new carcharodontosaurid (Dinosauria, Theropoda) from the Upper Cretaceous of Argentina". Geodiversitas 28: 71–118. https://www.researchgate.net/publication/228655543_A_new_carcharodontosaurid_Dinosauria_Theropoda_from_the_Upper_Cretaceous_of_Argentina. Retrieved 2019-02-16. 
  15. ↑ Sánchez, María Lidia; Heredia, Susana; Calvo, Jorge O. (2006). "Paleoambientes sedimentarios del Cretácico Superior de la Formación Plottier (Grupo Neuquén), Departamento Confluencia, Neuquén". pp. 3–18. https://www.researchgate.net/publication/262615949_Paleoambientes_sedimentarios_del_Cretacico_Superior_de_la_Formacion_Plottier_Grupo_Neuquen_Departamento_Confluencia_Neuquen. Retrieved 2019-02-16. 
  16. ↑ Leanza, H.A.; Apesteguia, S.; Novas, F.E.; De la Fuente, M.S. (2004). "Cretaceous terrestrial beds from the Neuquén Basin (Argentina) and their tetrapod assemblages". Cretaceous Research 25: 61–87. https://www.researchgate.net/publication/257047651_Cretaceous_terrestrial_beds_from_the_Neuquen_Basin_Argentina_and_their_tetrapod_assemblages. Retrieved 2019-02-16. 
  17. ↑ Vallati, P. (2001). "Middle cretaceous microflora from the Huincul Formation ("Dinosaurian Beds") in the Neuquén Basin, Patagonia, Argentina". Palynology 25 (1): 179–197. doi:10.2113/0250179. Bibcode: 2001Paly...25..179V. https://www.researchgate.net/publication/241723727. 
  18. ↑ Motta, M.J.; Brissón Egli, F.; Aranciaga Rolando, A.M.; Rozadilla, S.; Gentil, A. R.; Lio, G.; Cerroni, M.; Garcia Marsà, J. et al. (2019). "New vertebrate remains from the Huincul Formation (Cenomanian–Turonian;Upper Cretaceous) in Río Negro, Argentina". Publicación Electrónica de la Asociación Paleontológica Argentina 19 (1): R26. doi:10.5710/PEAPA.15.04.2019.295. http://www.peapaleontologica.org.ar/index.php/peapa/article/viewFile/295/355. Retrieved December 14, 2019. 
  19. ↑ Bellardini, F.; Filippi, L.S. (2018). "New evidence of saurischian dinosaurs from the upper member of the Huincul Formation (Cenomanian) of Neuquén Province, Patagonia, Argentina". Reunión de Comunicaciones de la Asociación Paleontológica Argentina: 10. 
  20. ↑ Carrano, Matthew (2016). "Violante farm (Cretaceous of Argentina) Also known as Violante’s farm, Pueblo Blanco Natural Reserve". https://paleobiodb.org/classic/basicCollectionSearch?collection_no=180530. 
  21. ↑ Calvo, Jorge Orlando; Valieri, Ruben D. Juarez; Ríos, Sergio D. (2011). "Sauropods crossing formations: Biostratigraphical implications for Patagonian Faunal Assemblages". Paleontología y Dinosaurios desde América Latina [Paleontology and Dinosaurs from Latin America]. EDIUNC, Universidad Nacional de Cuyo. p. 153-160. https://www.researchgate.net/publication/261699297. 
  22. ↑ Salgado, Leonardo (2023). "A new gigantic titanosaur (Dinosauria, Sauropoda) from the early Late Cretaceous of Patagonia (Neuquén Province, Argentina)". Acta Palaeontologica Polonica 68. doi:10.4202/app.01086.2023. 
  23. ↑ Lerzo, Lucas Nicolás; Gallina, Pablo Ariel; Canale, Juan Ignacio; Otero, Alejandro; Carballido, José Luis; Apesteguía, Sebastián; Makovicky, Peter Juraj (2024-01-03). "The last of the oldies: a basal rebbachisaurid (Sauropoda, Diplodocoidea) from the early Late Cretaceous (Cenomanian–Turonian) of Patagonia, Argentina" (in en). Historical Biology: 1–26. doi:10.1080/08912963.2023.2297914. ISSN 0891-2963. 
  24. ↑ Canale, Juan I.; Apesteguía, Sebastián; Gallina, Pablo A.; Mitchell, Jonathan; Smith, Nathan D.; Cullen, Thomas M.; Shinya, Akiko; Haluza, Alejandro et al. (July 2022). "New giant carnivorous dinosaur reveals convergent evolutionary trends in theropod arm reduction". Current Biology 32 (14): 3195–3202.e5. doi:10.1016/j.cub.2022.05.057. PMID 35803271. 

Wikidata ☰ Q95715804 entry



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