Editing Carnotaurus

{{short description|Genus of dinosaur from the Late Cretaceous period}}
{{Distinguish|Carnosaurus}}
{{featured article}}
{{Use American English|date=September 2020}}
{{Use mdy dates|date=July 2023}}
{{speciesbox
| fossil_range = [[Late Cretaceous]] ([[Maastrichtian]]),<ref name="Cerroni2020"/> {{fossil range|72|69|latest=66}}
| image = Carnotaurus skeleton LA.jpg
| image_upright = 1.1
| image_caption = Mounted skeletal cast at [[Natural History Museum of Los Angeles County]]
| image_alt = Skeleton cast
| genus = Carnotaurus
| display_parents = 3
| parent_authority = [[José Bonaparte|Bonaparte]], 1985
| species = sastrei
| authority = Bonaparte, 1985
}}

'''''Carnotaurus''''' ({{IPAc-en|ˌ|k|ɑːr|n|oʊ-|ˈ|t|ɔːr|ə|s}}; {{lit|meat bull}}) is a [[genus]] of [[Theropoda|theropod]] [[dinosaur]] that lived in [[South America]] during the [[Late Cretaceous]] period, probably sometime between 72 and 69 million years ago. The only [[species]] is '''''Carnotaurus sastrei'''''. Known from a single well-preserved skeleton, it is one of the best-understood theropods from the [[Southern Hemisphere]]. The skeleton, found in 1984, was uncovered in the [[Chubut Province]] of [[Argentina]] from rocks of the [[La Colonia Formation]]. ''Carnotaurus'' is a derived member of the [[Abelisauridae]], a group of large theropods that occupied the large [[predation|predatorial]] [[ecological niche|niche]] in the southern landmasses of [[Gondwana]] during the late [[Cretaceous]]. Within the Abelisauridae, the genus is often considered a member of the Brachyrostra, a clade of short-snouted forms restricted to South America.

''Carnotaurus'' was a lightly built, [[biped]]al predator, measuring {{convert|7.5|to|8|m|ft|1|abbr=on}} in length and weighing {{convert|1.3|-|2.1|MT|ST + LT}}. As a theropod, ''Carnotaurus'' was highly specialized and distinctive. It had two thick [[horn (anatomy)|horns]] above the eyes, a unique feature unseen in all other [[carnivore|carnivorous]] dinosaurs, and a very deep skull sitting on a muscular neck. ''Carnotaurus'' was further characterized by small, [[vestigiality|vestigial]] forelimbs and long, slender hind limbs. The skeleton is preserved with extensive skin impressions, showing a mosaic of small, non-overlapping [[scale (anatomy)|scales]] approximately 5&nbsp;mm in diameter. The mosaic was interrupted by large bumps that lined the sides of the animal, and there are no hints of feathers.

The distinctive horns and the muscular neck may have been used in fighting others of its species. According to separate studies, rivaling individuals may have combated each other with quick head blows, by slow pushes with the upper sides of their skulls, or by ramming each other head-on, using their horns as shock absorbers. The feeding habits of ''Carnotaurus'' remain unclear: some studies suggested the animal was able to hunt down very large prey such as [[sauropod]]s, while other studies found it preyed mainly on relatively small animals. Its brain cavity suggests an acute sense of smell, while hearing and sight were less well developed. ''Carnotaurus'' was probably well adapted for running and was possibly one of the fastest large theropods.

==Discovery==
[[File:DinosaursCalci.JPG|thumb|left|alt=Skeletal casts of ''Amargasaurus'' and ''Carnotaurus'' |Casts of ''[[Amargasaurus]]'' and ''Carnotaurus'', both discovered by the same 1984 expedition in Argentina, [[Natural History Museum of the University of Pisa]]]]
The only skeleton ([[holotype]] [[Bernardino Rivadavia Natural Sciences Argentine Museum|MACN]]-CH 894) was unearthed in 1984 by an expedition led by Argentinian paleontologist [[José Bonaparte]].{{efn-ua|p. 276 in Novas (2009)<ref name="novas2009"/>}} This expedition also recovered the peculiar spiny [[sauropod]] ''[[Amargasaurus]]''.<ref name="salgadobonaparte1991"/> It was the eighth expedition within the project named "Jurassic and Cretaceous Terrestrial Vertebrates of South America", which started in 1976 and was sponsored by the [[National Geographic Society]].<ref name="salgadobonaparte1991"/>{{efn-ua|p. 2 in Bonaparte (1990)<ref name="bonaparte1990" />}} The skeleton is well-preserved and {{Dinogloss|articulated}} (still connected together), with only the posterior two thirds of the tail, much of the lower leg, and the hind feet being destroyed by [[weathering]].{{efn-ua|p. 2 in Bonaparte (1990)<ref name="bonaparte1990" />}}<ref name="bonaparte1985"/> The skeleton belonged to an adult individual, as indicated by the fused [[suture (anatomy)|sutures]] in the {{Dinogloss|braincase}}.<ref name="carabajal2011"/> It was found lying on its right side, showing a typical [[death pose]] with the neck bent back over the torso.<ref name="czerkas1997"/> Unusually, it is preserved with extensive skin impressions.{{efn-ua|p. 2 in Bonaparte (1990)<ref name="bonaparte1990" />}} In view of the significance of these impressions, a second expedition was started to reinvestigate the original excavation site, leading to the recovery of several additional skin patches.<ref name="czerkas1997"/> The skull was deformed during fossilization, with the snout bones of the left side displaced forwards relative to the right side, the nasal bones pushed upwards, and the {{Dinogloss|premaxillae}} pushed backwards onto the {{Dinogloss|nasal bones}}. Deformation also exaggerated the upward curvature of the upper jaw.{{efn-ua|p. 191 in Carrano and Sampson (2008)<ref name="carrano2008"/>}} The snout was more strongly affected by deformation than the rear part of the skull, possibly due to the higher rigidity of the latter. In top or bottom view, the upper jaws were less U-shaped than the lower jaws, resulting in an apparent mismatch. This mismatch is the result of deformation acting from the sides, which affected the upper jaws but not the lower jaws, possibly due to the greater flexibility of the joints within the latter.<ref name="Cerroni2020"/>

[[File:Carnotaurus reconstruction Headden.jpg|thumb|Illustration of the known material of ''Carnotaurus'']]
The skeleton was collected on a farm named "Pocho Sastre" near Bajada Moreno in the [[Telsen Department]] of [[Chubut Province]], Argentina.<ref name="bonaparte1985"/> Because it was embedded in a large [[hematite]] [[concretion]], a very hard kind of rock, preparation was complicated and progressed slowly.<ref name="Paul1988PDW"/><ref name="bonaparte1985"/> In 1985, Bonaparte published a note presenting ''Carnotaurus sastrei'' as a new genus and species and briefly describing the skull and lower jaw.<ref name="bonaparte1985"/> The generic name ''Carnotaurus'' is derived from the Latin carno [carnis] ("flesh") and taurus ("bull") and can be translated with "meat-eating bull", an allusion to the animal's bull-like horns.<ref name="yong"/> The [[specific name (zoology)|specific name]] ''sastrei'' honors Angel Sastre, the owner of the ranch where the skeleton was found.<ref name="headden2006"/> A comprehensive description of the whole skeleton followed in 1990.<ref name="bonaparte1990" /> After ''[[Abelisaurus]]'', ''Carnotaurus'' was the second member of the family Abelisauridae that was discovered.<ref name="bonaparte1991"/> For years, it was by far the best-understood member of its family, and also the best-understood theropod from the [[Southern Hemisphere]].<ref name="bonaparte1996"/><ref name="glut1997"/> It was not until the 21st century that similar well-preserved [[Abelisauridae|abelisaurids]] were described, including ''[[Aucasaurus]]'', ''[[Majungasaurus]]'' and ''[[Skorpiovenator]]'', allowing scientists to re-evaluate certain aspects of the anatomy of ''Carnotaurus''.{{efn-ua|p. 191 in Carrano and Sampson (2008)<ref name="carrano2008"/>}} The holotype skeleton is displayed in the [[Argentine Museum of Natural Sciences]], [[Bernardino Rivadavia]];{{efn-ua|p. 3 in Bonaparte (1990)<ref name="bonaparte1990" />}} replicas can be seen in this and other museums around the world.<ref name="glut2003"/> Sculptors Stephen and Sylvia Czerkas manufactured a life-sized sculpture of ''Carnotaurus'' that was previously on display at the [[Natural History Museum of Los Angeles County]]. This sculpture, ordered by the museum during the mid-1980s, is probably the first life restoration of a theropod showing accurate skin.<ref name="czerkas1997"/><ref name="glut2000"/>

==Description==
[[File:Carnotaurus_Size_Chart.png|thumb|alt=Size comparison of ''Carnotaurus''|Scale diagram comparing ''Carnotaurus'' to a human]]
''Carnotaurus'' was a large but lightly built predator.<ref name="candeiro2005"/> The only known individual was about {{convert|7.5|-|8|m|ft|1|abbr=on}} in length,{{efn-ua|p. 38 in Bonaparte (1990)<ref name="bonaparte1990" />}}{{efn-ua|p. 162 in Juárez Valieri et al. (2010)<ref name="valieri2010" />}}<ref name="G.S.Paul2010">{{cite book |last=Paul |first=Gregory S. |author-link=Gregory S. Paul |date=2010 |title=The Princeton Field Guide to Dinosaurs |title-link=The Princeton Field Guide to Dinosaurs |edition=1st |publisher=Princeton University Press |isbn=9780691137209}}</ref> making ''Carnotaurus'' one of the largest abelisaurids.{{efn-ua|p. 191 in Carrano and Sampson (2008)<ref name="carrano2008"/>}}{{efn-ua|p. 162 in Juárez Valieri et al. (2010)<ref name="valieri2010" />}}<ref name="G.S.Paul2010" /> ''[[Ekrixinatosaurus]]'' and possibly ''[[Abelisaurus]]'', which are highly incomplete, might have been similar or larger in size.{{efn-ua|p. 163 in Juárez Valieri et al. (2010)<ref name="valieri2010" />}}{{efn-ua|p. 556 in Calvo et al. (2004)<ref name="calvoetal2004"/>}}{{efn-ua|p. 191 in Carrano and Sampson (2008)<ref name="carrano2008"/>}} A 2016 study found that only ''[[Pycnonemosaurus]]'', at {{convert|8.9|m|ft|1|abbr=on}}, was longer than ''Carnotaurus''; it was estimated at {{convert|7.8|m|ft|1|abbr=on}}.<ref>{{cite journal |last1=Grillo |first1=O.N. |last2=Delcourt |first2=R. |date=2016 |title=Allometry and body length of abelisauroid theropods: ''Pycnonemosaurus nevesi'' is the new king |journal=Cretaceous Research |doi=10.1016/j.cretres.2016.09.001 |volume=69 |pages=71–89|bibcode=2017CrRes..69...71G }}</ref> Its mass is estimated to have been {{convert|1,350|kg|ton|abbr=on}},{{efn-ua|p. 30 in Bonaparte (1990)<ref name="bonaparte1990" />}} {{convert|1,500|kg|ton|abbr=on}},{{efn-ua|p. 187 in Mazzetta et al. (1998)<ref name="GVPaleobiology"/>}} {{convert|2,000|kg|ton|abbr=on}},<ref name="G.S.Paul2010" /> {{convert|2,100|kg|ton|abbr=on}},{{efn-ua|p. 79 in Mazzetta et al. (2004)<ref name="mazzettaetal2004"/>}} and {{convert|1,306|-|1743|kg|ton|abbr=on}}<ref name="Cerroni2019">{{cite journal |last1=Cerroni |first1=Mauricio A. |last2=Paulina-Carabajal |first2=Ariana |date=2019 |title=Novel information on the endocranial morphology of the abelisaurid theropod ''Carnotaurus sastrei'' |journal=Comptes Rendus Palevol |doi=10.1016/j.crpv.2019.09.005 |volume=18 |issue=8 |pages=985–995|doi-access= |bibcode=2019CRPal..18..985C }}</ref> in separate studies that used different estimation methods. ''Carnotaurus'' was a highly specialized theropod, as seen especially in characteristics of the [[skull]], the [[vertebra]]e and the forelimbs.{{efn-ua|p. 276 in Novas (2009)<ref name="novas2009"/>}} The [[pelvis]] and hind limbs, on the other hand, remained relatively conservative, resembling those of the more [[basal (phylogenetics)|basal]] ''[[Ceratosaurus]]''. Both the pelvis and hind limb were long and slender. The left {{Dinogloss|femur}} (thigh bone) of the individual measures 103&nbsp;cm in length, but shows an average diameter of only 11&nbsp;cm.{{efn-ua|p. 28–32 in Bonaparte (1990)<ref name="bonaparte1990" />}}

===Skull===
[[File:Carnotaurus skull.jpg|thumb|left|alt=Side of skull|Skull in multiple views, with details of the skin structures inferred, and the right frontal horn]]
The skull, measuring {{convert|59.6|cm|in|abbr=on}} in length, was proportionally shorter and deeper than in any other large carnivorous dinosaur.{{efn-ua|p. 8 in Bonaparte (1990)<ref name="bonaparte1990" />}}{{efn-ua|p. 191 in Carrano and Sampson (2008)<ref name="carrano2008"/>}} The [[snout]] was moderately broad, not as tapering as seen in more basal theropods like ''Ceratosaurus'', and the jaws were curved upwards.<ref name="sampson2007"/> A prominent pair of horns protruded obliquely above the eyes. These horns, formed by the [[frontal bone#In dinosaurs|frontal]] bones,{{efn-ua|p. 4–5 in Bonaparte (1990)<ref name="bonaparte1990" />}} were thick and cone-shaped, internally solid, somewhat vertically flattened in cross-section, and measured {{convert|15|cm|in|abbr=on}} in length.<ref name="carabajal2011"/><ref name="Cerroni2020"/> Bonaparte, in 1990, suggested that these horns would probably have formed the bony cores of much longer keratinous sheaths.{{efn-ua|p. 5 in Bonaparte (1990)<ref name="bonaparte1990" />}}  Mauricio Cerroni and colleagues, in 2020, agreed that the horns supported keratinous sheaths, but argued that these sheaths would not have been greatly longer than the bony cores.<ref name="Cerroni2020"/>

As in other dinosaurs, the skull was perforated by six [[Skull#Fenestrae|major skull openings]] on each side. The frontmost of these openings, the {{Dinogloss|external naris}} (bony nostril), was subrectangular and directed sidewards and forwards, but was not sloping in side view as in some other ceratosaurs such as ''Ceratosaurus''. This opening was formed by the nasal and premaxilla only, while in some related ceratosaurs the maxilla also contributed to this opening. Between the bony nostril and the [[orbit (anatomy)|orbit]] (eye opening) was the [[antorbital fenestra]]. In ''Carnotaurus'', this opening was higher than long, while it was longer than high in related forms such as ''Skorpiovenator'' and ''Majungasaurus''. The antorbital fenestra was bounded by a larger depression, the {{Dinogloss|antorbital fossa}}, which was formed by recessed parts of the maxilla in front and the {{Dinogloss|lacrimal}} behind. As in all abelisaurids, this depression was small in ''Carnotaurus''. The lower front corner of the antorbital fossa contained a smaller opening, the {{Dinogloss|promaxillary fenestra}}, which led into an air-filled cavity within the maxilla.<ref name="Cerroni2020"/> The eye was situated in the upper part of the keyhole-shaped orbit.{{efn-ua|p. 3 in Bonaparte (1990)<ref name="bonaparte1990" />}} This upper part was proportionally small and subcircular, and separated from the lower part of the orbit by the forward-projecting {{Dinogloss|postorbital bone}}.<ref name="Cerroni2020"/> It was slightly rotated forward, probably permitting some degree of [[binocular vision]].{{efn-ua|p. 191 in Mazzetta et al. (1998)<ref name="GVPaleobiology"/>}} The keyhole-like shape of the orbit was possibly related to the marked skull shortening, and is also found in related short-snouted abelisaurids.<ref name="Cerroni2020"/> As in all abelisaurids, the {{Dinogloss|frontal bone}} (on the skull roof between the eyes) was excluded from the orbit. Behind the orbit were two openings, the {{Dinogloss|infratemporal fenestra}} on the side and the {{Dinogloss|supratemporal fenestra}} on the top of the skull. The infratemporal fenestra was tall, short, and kidney-shaped, while the supratemporal fenestra was short and square-shaped. Another opening, the {{Dinogloss|mandibular fenestra}}, was located in the lower jaw – in ''Carnotaurus'', this opening was comparatively large.<ref name="Cerroni2020"/>

[[File:Carnotaurus skull diagram.svg|thumb|upright=1.2|Schematic diagram of reconstructed skull]]
On each side of the upper jaws there were four [[premaxilla]]ry and twelve [[maxilla]]ry teeth,{{efn-ua|p. 255 in Novas (2009)<ref name="novas2009"/>}} while the [[lower jaw]]s were equipped with fifteen [[dentary]] teeth per side.{{efn-ua|p. 6 in Bonaparte (1990)<ref name="bonaparte1990" />}}<ref name="Cerroni2020"/> The teeth had been described as being long and slender,<ref name="Paul1988PDW"/> as opposed to the very short teeth seen in other abelisaurids.<ref name="sampson2007"/> However, Cerroni and colleagues, in their 2020 description of the skull, stated that all [[Tooth eruption|erupted]] teeth have been severely damaged during excavation and were later reconstructed with plaster (Bonaparte, in 1990, only noted that some lower jaw teeth had been fragmented).<ref name="Cerroni2020"/>{{efn-ua|p. 6 in Bonaparte (1990)<ref name="bonaparte1990" />}} Reliable information on the shape of the teeth is therefore limited to replacement teeth and tooth roots that are still enclosed by the jaw, and can be studied using CT imaging.<ref name="Cerroni2020"/> The replacement teeth had low, flattened [[tooth crown|crowns]], were closely spaced, and inclined forwards at approximately 45°.<ref name="Cerroni2020"/> In his 1990 description, Bonaparte noted that the lower jaw was shallow and weakly constructed, with the {{Dinogloss|dentary}} (the foremost jaw bone) connected to the hindmost jaw bones by only two contact points; this contrasts to the robust-looking skull.<ref name="Paul1988PDW"/>{{efn-ua|p. 6 in Bonaparte (1990)<ref name="bonaparte1990" />}} Cerroni and colleagues instead found multiple but loose connections between the dentary and the hindmost jaw bones. This articulation, therefore, was very flexible but not necessarily weak.<ref name="Cerroni2020">{{cite journal |last1=Cerroni |first1=M. A. |last2=Canale |first2=J. I. |last3=Novas |first3=F. E. |date=2020 |title=The skull of ''Carnotaurus sastrei'' Bonaparte 1985 revisited: insights from craniofacial bones, palate and lower jaw |journal=Historical Biology |volume=33 |issue=10 |doi=10.1080/08912963.2020.1802445 |pages=2444–2485 |s2cid=225374445 |url=https://figshare.com/articles/dataset/The_skull_of_i_Carnotaurus_sastrei_i_Bonaparte_1985_revisited_insights_from_craniofacial_bones_palate_and_lower_jaw/12848981 |archive-date=March 6, 2023 |access-date=July 20, 2022 |archive-url=https://web.archive.org/web/20230306234111/https://figshare.com/articles/dataset/The_skull_of_i_Carnotaurus_sastrei_i_Bonaparte_1985_revisited_insights_from_craniofacial_bones_palate_and_lower_jaw/12848981 |url-status=live |url-access=subscription }}</ref> The bottom margin of the dentary was convex, while it was straight in ''Majungasaurus''.<ref name="Cerroni2020"/>

[[File:Carnotaurus Reconstruction (2022).png|thumb|left|alt=Illustration|[[Life restoration]]]]
The lower jaw was found with [[ossification|ossified]] [[hyoid bone]]s, in the position they would be in if the animal was alive. These slender bones, supporting the tongue musculature and several other muscles, are rarely found in dinosaurs because they are often [[cartilage|cartilaginous]] and not connected to other bones and therefore get lost easily.{{efn-ua|p. 6 in Bonaparte (1990)<ref name="bonaparte1990" />}}<ref name="hartman2012"/><ref name="Cerroni2020"/> In ''Carnotaurus'', three hyoid bones are preserved: a pair of curved, rod-like ceratobranchials that articulate with a single, trapezoidal element, the basihyal. ''Carnotaurus'' is the only known non-avian theropod from which a basihyal is known.<ref name="Cerroni2020"/> The back of the skull had well-developed, air-filled chambers surrounding the braincase, as in other abelisaurids. Two separate chamber systems were present, the paratympanic system, which was connected to the [[middle ear]] cavity, as well as chambers resulting from outgrowths of the [[air sac]]s of the neck.<ref name="Cerroni2019"/>

A number of [[autapomorphy|autapomorphies]] (distinguishing features) can be found in the skull, including the pair of horns and the very short and deep skull. The maxilla had excavations above the promaxillary fenestra, which would have been excavated by the antorbital air sinus (air passages in the snout). The nasolacrimal duct, which transported eye fluid, exited on the medial (inner) surface of the lacrimal through a canal of uncertain function. Other proposed autapomorphies include a deep and long, air-filled excavation in the {{Dinogloss|quadrate}} and an elongated depression on the {{Dinogloss|pterygoid}} of the {{Dinogloss|palate}}.<ref name="Cerroni2020"/>

===Vertebrae===
[[File:Carnotaurus-tail-vertebra-caudal-ribs.png|thumb|alt=Three views of the caudal ribs on vertebrae|Sixth tail vertebra of the [[holotype]] in A) side, B) front and C) top views, with arrows indicating the highly modified caudal ribs]]
The vertebral column consisted of ten [[cervical vertebrae|cervical]] (neck), twelve [[thoracic vertebrae|dorsal]], six fused [[Sacrum#Other animals|sacral]]{{efn-ua|p. 191 in Carrano and Sampson (2008)<ref name="carrano2008"/>}} and an unknown number of [[coccyx|caudal]] (tail) vertebrae.<ref name="bonaparte1990" /> The neck was nearly straight, rather than having the S-curve seen in other theropods, and also unusually wide, especially towards its base.<ref name="mendez"/> The top of the neck's spinal column featured a double row of enlarged, upwardly directed bony processes called [[epipophyses]], creating a smooth trough on the top of the neck vertebrae. These processes were the highest points of the spine, towering above the unusually low [[spinous process]]es.<ref name="bonaparte1990" /><ref name="hartman2012"/> The epipophyses probably provided attachment areas for a markedly strong neck musculature.{{efn-ua|pp. 257 in Novas (2009)<ref name="novas2009"/>}} A similar double row was also present in the tail, formed there by highly modified [[transverse processes|caudal ribs]], in front view protruding upwards in a V-shape, their inner sides creating a smooth, flat, top surface of the front tail vertebrae. The end of each caudal rib was furnished with a forward projecting hook-shaped expansion that connected to the caudal rib of the preceding vertebra.<ref name="hartman2012"/><ref name="personscurrie2011"/>

===Forelimbs===

{{multiple image
|align = right
|total_width = 350
|image1 = Forelimb of Carnotaurus.jpg
|alt1 = Cross-section of the tail muscles
|image2 = Carnotaurus manus.svg
|alt2 = Drawing of the hand bones
|footer = Forelimb bones (left) and hand bones as interpreted by Ruiz and colleagues (2011)<ref name="ruiz2011"/>
}}

The forelimbs were proportionally shorter than in any other large carnivorous dinosaurs, including tyrannosaurids.{{efn-ua|p. 1276 in Ruiz et al. (2011)<ref name="ruiz2011"/>}} The forearm was only a quarter the size of the upper arm. There were no [[Carpal bones|carpalia]] in the hand, so that the [[metacarpus|metacarpals]] articulated directly with the forearm.<ref name="ruiz2011"/> The hand showed four basic digits,<ref name="bonaparte1990" /> though apparently only the middle two of these ended in finger bones, while the fourth consisted of a single splint-like metacarpal that may have represented an external 'spur'. The fingers themselves were fused and immobile, and may have lacked claws.<ref name="agnolin&chiarelli2010" /> ''Carnotaurus'' differed from all other abelisaurids in having proportionally shorter and more robust forelimbs, and in having the fourth, splint-like metacarpal as the longest bone in the hand.<ref name="ruiz2011"/> A 2009 study suggests that the arms were [[vestigiality|vestigial]] in abelisaurids, because nerve fibers responsible for stimulus transmission were reduced to an extent seen in today's [[emu]]s and [[Kiwi (bird)|kiwi]]s, which also have vestigial forelimbs.<ref name="senter2010"/>

===Skin===
''Carnotaurus'' was the first theropod dinosaur discovered with a significant number of [[fossil]] skin impressions.<ref name="czerkas1997"/> These impressions, found beneath the skeleton's right side, come from different body parts, including the lower jaw,<ref name="czerkas1997"/> the front of the neck, the [[shoulder girdle]], and the [[rib cage]].{{efn-ua|p. 32 in Bonaparte (1990)<ref name="bonaparte1990" />}} The largest patch of skin corresponds to the anterior part of the tail.{{efn-ua|p. 32 in Bonaparte (1990)<ref name="bonaparte1990" />}} Originally, the right side of the skull also was covered with large patches of skin—this was not recognized when the skull was prepared, and these patches were accidentally destroyed.<ref name="czerkas1997"/> However, the [[surface texture]] of several skull bones allows for inferences on their probable covering. A hummocky surface with grooves, pits, and small openings is found on the sides and front of the snout and indicates a scaly covering, possibly with flat scales as in today's crocodilians. The top of the snout was sculptured with numerous small holes and spikes – this texture can probably be correlated with a cornified pad (horny covering). Such a pad also occurred in ''Majungasaurus'' but was absent in ''[[Abelisaurus]]'' and ''Rugops''. A row of large scales did probably surround the eye, as indicated by a hummocky surface with longitudinal grooves on the lacrimal and postorbital bones.<ref name="Cerroni2020"/>{{efn-ua|p. 3 in Bonaparte (1990)<ref name="bonaparte1990" />}}
[[File:Carnotaurus skin.jpg|thumb|left|Skin impressions from the tail]]
The skin was built up of a mosaic of polygonal, non-overlapping scales measuring approximately {{convert|5–12|mm|in|abbr=on}} in diameter. This mosaic was divided by thin, parallel grooves.{{efn-ua|pp. 264–299 in Novas (2009)<ref name="novas2009"/>}} Scalation was similar across different body parts with the exception of the head, which apparently showed a different, irregular pattern of scales.{{efn-ua|pp. 264–299 in Novas (2009)<ref name="novas2009"/>}}<ref name="glut2003"/> There is no evidence of feathers.<ref name="czerkas1997"/> Larger bump-like structures were distributed over the sides of the neck, back and tail in irregular rows. These bumps were {{convert|4|to|5|cm|in|abbr=on}} in diameter and up to {{convert|5|cm|abbr=on}} in height and often showed a low midline ridge. They were set {{convert|8|to|10|cm|in|abbr=on}} apart from each other and became larger towards the animal's top. The bumps probably represent feature scales – clusters of condensed [[scute]]s – similar to those seen on the soft frill running along the body midline in [[hadrosaurid]] ("duck-billed") dinosaurs. These structures did not contain bone.{{efn-ua|p. 32 in Bonaparte (1990)<ref name="bonaparte1990" />}}<ref name="czerkas1997"/><ref name="champione2020">{{Cite book| publisher = Springer| isbn = 978-3-030-27222-7| pages = 213–243 |editor=Christian Foth |editor2=Oliver W.M. Rauhut | last1 = Campione| first1 = Nicolás E.| last2 = Barrett| first2 = Paul M.| last3 = Evans| first3 = David C.| title = The Evolution of Feathers| chapter = On the ancestry of feathers in Mesozoic dinosaurs| date = 2020}}</ref> Stephen Czerkas (1997) suggested that these structures may have protected the animal's sides while fighting members of the same species ([[Conspecificity|conspecifics]]) and other theropods, arguing that similar structures can be found on the neck of the modern [[iguana]] where they provide limited protection in combat.<ref name="czerkas1997"/>

More recent studies of the skin of ''Carnotaurus'' published in 2021 suggest that previous depictions of the scales on the body are inaccurate, and the larger feature scales were randomly distributed along the body, not distributed in discrete rows like in older artistic depictions and illustrations. There is also no sign of progressive size variation in feature scales along different areas along the body. The basement scales of ''Carnotaurus'' were by comparison highly variable, ranging in size from small and elongated, to large and polygonal, and from circular-to-lenticular in the thoracic, scapular, and tail regions, respectively. This scale differentiation may have been related to regulating body heat and shedding excess heat via thermoregulation due to its large body size and active lifestyle.<ref>{{cite journal |last1=Hendrickx |first1=Christophe |last2=Bell |first2=Phil R. |title=The scaly skin of the abelisaurid Carnotaurus sastrei (Theropoda: Ceratosauria) from the Upper Cretaceous of Patagonia |journal=Cretaceous Research |date=August 2021 |volume=128 |pages=104994 |doi=10.1016/j.cretres.2021.104994 |bibcode=2021CrRes.12804994H }}</ref>

==Classification==
[[File:Carnotaurus Los Angeles County Museum 15.jpg|thumb|right|Mount in LA seen from above]]
''Carnotaurus'' is one of the best-understood [[genus|genera]] of the [[Abelisauridae]], a family of large theropods restricted to the ancient southern [[supercontinent]] [[Gondwana]]. Abelisaurids were the dominant predators in the Late Cretaceous of Gondwana, replacing the [[Carcharodontosauridae|carcharodontosaurids]] and occupying the ecological niche filled by the [[Tyrannosauridae|tyrannosaurids]] in the northern continents.<ref name="candeiro2005"/> Several notable traits that evolved within this family, including shortening of the skull and arms as well as peculiarities in the cervical and caudal vertebrae, were more pronounced in ''Carnotaurus'' than in any other abelisaurid.{{efn-ua|p. 276–277 in Novas (2009)<ref name="novas2009"/>}}{{efn-ua|pp. 256–261 in Novas (2009)<ref name="novas2009"/>}}<ref name="personscurrie2011"/>

Though relationships within the Abelisauridae are debated, ''Carnotaurus'' is consistently shown to be one of the most [[derived trait|derived]] members of the family by cladistical analyses.{{efn-ua|pp. 188–189 and 202 in Carrano and Sampson (2008)<ref name="carrano2008"/>}} Its nearest relative might have been ''[[Aucasaurus]]''<ref name="canaleetal2009"/><ref name="coria2002"/><ref name="ezcurra2010"/><ref name="delcourt2018">{{cite journal |last=Delcourt |first=Rafael |date=2018 |title=Ceratosaur palaeobiology: new insights on evolution and ecology of the southern rulers |journal=Scientific Reports |pmid=29950661 |pmc=6021374 |doi=10.1038/s41598-018-28154-x |bibcode=2018NatSR...8.9730D |volume=8 |issue=1 |page=9730}}</ref> or ''[[Majungasaurus]]''.<ref name="sereno2004"/><ref name=tykoskirowe2004/><ref name="wilson2003"/> A 2008 review, in contrast, suggested that ''Carnotaurus'' was not closely related to either genus, and instead proposed ''[[Ilokelesia]]'' as its [[sister taxon]].{{efn-ua|p. 202 in Carrano and Sampson (2008)<ref name="carrano2008"/>}} Juan Canale and colleagues, in 2009, erected the new clade Brachyrostra to include ''Carnotaurus'' but not ''Majungasaurus''; this classification has been followed by a number of studies since.<ref name="canaleetal2009"/><ref name="delcourt2018"/><ref name="wang2017">{{cite journal |last1=Wang |first1=Shuo |last2=Stiegler |first2=Josef |last3=Amiot |first3=Romain |last4=Wang |first4=Xu |last5=Du |first5=Guo-hao |last6=Clark |first6=James M. |last7=Xu |first7=Xing |title=Extreme Ontogenetic Changes in a Ceratosaurian Theropod |journal=Current Biology |date=January 2017 |volume=27 |issue=1 |pages=144–148 |doi=10.1016/j.cub.2016.10.043 |pmid=28017609 |doi-access=free |bibcode=2017CBio...27..144W }}</ref>

''Carnotaurus'' is eponymous for two subgroups of the Abelisauridae: the [[Carnotaurinae]] and the [[Carnotaurini]]. Paleontologists do not universally accept these groups. The Carnotaurinae was defined to include all derived abelisaurids with the exclusion of ''[[Abelisaurus]]'', which is considered a basal member in most studies.<ref name="sereno_carnotaurinae"/> However, a 2008 review suggested that ''[[Abelisaurus]]'' was a derived abelisaurid instead.{{efn-ua|p. 202 in Carrano and Sampson (2008)<ref name="carrano2008"/>}} Carnotaurini was proposed to name the [[clade]] formed by ''Carnotaurus'' and ''Aucasaurus'';<ref name="coria2002"/> only those paleontologists who consider ''Aucasaurus'' as the nearest relative of ''Carnotaurus'' use this group.<ref name="sereno_carnotaurini"/> A 2024 study recovered Carnotaurini as a valid clade consisting of ''Carnotaurus'', ''Aucasaurus'', ''[[Niebla (dinosaur)|Niebla]]'' and ''[[Koleken]]''.<ref name="pol2024"/>

Below is a cladogram published by Canale and colleagues in 2009.<ref name="canaleetal2009"/>

{{clade| style=font-size:100%; line-height:85%
|label1=[[Carnotaurinae]]
|1={{clade
   |1=''[[Majungasaurus]]'' [[File:Majungasaurus BW (flipped).jpg|80 px]]
   |label2=[[Brachyrostra]]
   |2={{clade
      |label1=[[Carnotaurini]]
      |1={{clade
         |1=''[[Aucasaurus]]'' [[File:Aucasaurus garridoi by Paleocolour.jpg|80 px]]
         |2='''''Carnotaurus''''' [[File:Carnotaurus Reconstruction (2022).png|80 px]] }}
      |2={{clade
         |1=''[[Ilokelesia]]'' [[File:Ilokelesia (flipped).jpg|80 px]]
         |2={{clade
            |1=''[[Skorpiovenator]]'' [[File:Skorpiovenator bustingorryi.jpg|80 px]]
            |2=''[[Ekrixinatosaurus]]'' [[File:Ekrixinatosaurus novasi by Henrique Paes.png|80 px]] }} }} }} }} }}

==Paleobiology==

===Function of the horns===
[[File:Carnotaurus head.jpg|thumb|alt=Drawing of a ''Carnotaurus'' head|Restoration of the head showing the soft tissues inferred from osteological morphology of the skull]]
''Carnotaurus'' is the only known carnivorous bipedal animal with a pair of horns on the frontal bone.<ref name=GVMetal09/> The use of these horns is not entirely clear. Several interpretations have revolved around use in fighting conspecifics or in killing prey, though a use in display for courtship or recognition of members of the same species is possible as well.<ref name="Cerroni2020"/>

Greg Paul (1988) proposed that the horns were butting weapons and that the small orbita would have minimized the possibility of hurting the eyes while fighting.<ref name="Paul1988PDW"/> Gerardo Mazzetta and colleagues (1998) suggested that ''Carnotaurus'' used its horns in a way similar to rams. They calculated that the neck musculature was strong enough to absorb the force of two individuals colliding with their heads frontally at a speed of 5.7&nbsp;m/s each.<ref name="GVPaleobiology"/> Fernando Novas (2009) interpreted several skeletal features as [[adaptation]]s for delivering blows with the head.{{efn-ua|pp. 259–261 in Novas (2009)<ref name="novas2009"/>}} He suggested that the shortness of the skull might have made head movements quicker by reducing the [[moment of inertia]], while the muscular neck would have allowed strong head blows. He also noted an enhanced rigidity and strength of the spinal column that may have evolved to withstand shocks conducted by the head and neck.{{efn-ua|pp. 260–261 in Novas (2009)<ref name="novas2009"/>|group="upper-alpha"|}}

Other studies suggest that rivaling ''Carnotaurus'' did not deliver rapid head blows, but pushed slowly against each other with the upper sides of their skulls.<ref name=GVMetal09/><ref name="chure1998"/> Mazzetta and colleagues, in 2009, argued that the horns may have been a device for the distribution of compression forces without damage to the brain. This is supported by the flattened upper sides of the horns, the strongly fused bones of the top of the skull, and the inability of the skull to survive rapid head blows.<ref name=GVMetal09/> Rafael Delcourt, in 2018, suggested that the horns could have been used either in slow headbutting and shoving, as seen in the modern [[marine iguana]], or in blows to the opponent's neck and flanks, as seen in the modern [[giraffe]].<ref name="delcourt2018"/> The latter possibility had been previously proposed for the related ''Majungasaurus'' in a 2011 conference paper.<ref name="snively2011">{{Cite conference| publisher = American Society of Mechanical Engineers| volume = 54587| pages = 1075–1076| last1 = Snively| first1 = Eric| last2 = Cotton| first2 = John R.| last3 = Witmer| first3 = Lawrence| last4 = Ridgely| first4 = Ryan| last5 = Theodor| first5 = Jessica| title = Finite element comparison of cranial sinus function in the dinosaur ''Majungasaurus'' and head-clubbing giraffes| book-title = Summer Bioengineering Conference| date = 2011}}</ref>

Gerardo Mazzetta and colleagues (1998) propose that the horns might also have been used to injure or kill small prey. Though horn cores are blunt, they may have had a similar form to modern [[bovid]] horns if there was a [[keratin]]ous covering. However, this would be the only reported example of horns being used as hunting weapons in animals.<ref name="GVPaleobiology"/>

===Jaw function and diet===
[[File:Carnotaurus Skull.jpg|thumb|upright|alt=Cast of skull|Skull cast, [[Dinosaur Discovery Museum]], [[Kenosha, Wisconsin]]]]
Analyses of the jaw structure of ''Carnotaurus'' by Mazzetta and colleagues, in 1998, 2004, and 2009, suggest that the animal was capable of quick bites, but not strong ones.<ref name="GVPaleobiology"/><ref name="mazzettaetal2004"/><ref name=GVMetal09/> Quick bites are more important than strong bites when [[Dinosaur diet and feeding|capturing small prey]], as shown by studies of modern-day [[crocodile]]s.<ref name=GVMetal09/> These researchers also noted a high degree of flexibility ([[cranial kinesis|kinesis]]) within the skull and especially the lower jaw, somewhat similar to modern [[snake]]s. Elasticity of the jaw would have allowed ''Carnotaurus'' to swallow small prey items whole. In addition, the front part of the lower jaw was hinged, and thus able to move up and down. When pressed downwards, the teeth would have projected forward, allowing ''Carnotaurus'' to spike small prey items; when the teeth were curved upwards, the now backward projecting teeth would have hindered the caught prey from escaping.<ref name="GVPaleobiology"/> Mazzetta and colleagues also found that the skull was able to withstand forces that appear when tugging on large prey items.<ref name=GVMetal09/> ''Carnotaurus'' may therefore have fed mainly on relatively small prey, but also was able to hunt large dinosaurs.<ref name=GVMetal09/> In 2009, Mazzetta and colleagues estimated a bite force of around 3,341 newtons.<ref name=GVMetal09/> A 2022 study estimating bite force for 33 different dinosaurs suggests that the bite force in ''Carnotaurus'' was around 3,392 newtons at the anterior portion of the jaws; slightly higher than the previous estimate. The posterior bite force at the back of the jaws meanwhile, was estimated at 7,172 newtons.<ref>{{cite journal | doi=10.7717/peerj.13731 | title=Estimating bite force in extinct dinosaurs using phylogenetically predicted physiological cross-sectional areas of jaw adductor muscles | year=2022 | last1=Sakamoto | first1=Manabu | journal=PeerJ | volume=10 | pages=e13731 | pmid=35846881 | pmc=9285543 | doi-access=free }}</ref>

This interpretation was questioned by François Therrien and colleagues (2005), who found that the biting force of ''Carnotaurus'' was twice that of the [[American alligator]], which may have the strongest bite of any living [[tetrapod]]. These researchers also noted analogies with modern [[Komodo dragon]]s: the [[flexural strength]] of the lower jaw decreases towards the tip linearly, indicating that the jaws were not suited for high precision catching of small prey but for delivering slashing wounds to weaken big prey. As a consequence, according to this study, ''Carnotaurus'' must have mainly preyed upon large animals, possibly by ambush.<ref name="therrien2005"/> Cerroni and colleagues, in 2020, argued that flexibility was restricted to the lower jaw, while the thickened skull roof and the ossification of several cranial joints suggest that the skull had no or only little kinesis.<ref name="Cerroni2020"/>

[[Robert Bakker]] (1998) found that ''Carnotaurus'' mainly fed upon very large prey, especially [[sauropod]]s. As he noted, several adaptations of the skull—the short snout, the relatively small teeth and the strong back of the skull ([[occiput]])—had independently evolved in ''[[Allosaurus]]''. These features suggest that the upper jaw was used like a serrated club to inflict wounds; big sauropods would have been weakened by repeated attacks.<ref name="bakker1998" />

===Locomotion===

{{multiple image
|align = left
|total_width = 350
|image1 = Carnotaurus tail cross section.png
|alt1 = Cross-section of the tail muscles
|caption1 = Cross section through the tail of ''Carnotaurus'', showing the enlarged caudofemoralis muscle and the V-shaped caudal ribs
|image2 = Robustly modeled tail of Carnotaurus.png
|caption2 = 3D reconstructions of the tail muscles, tail, and pelvic bones seen from the side and above
|alt2 = 
}}

Mazzetta and colleagues (1998, 1999) presumed that ''Carnotaurus'' was a swift runner, arguing that the [[femur|thigh bone]] was adapted to withstand high [[bending moment]]s while running; The ability of an animal's leg to withstand those forces limits its top speed. The running adaptations of ''Carnotaurus'' would have been better than those of a human, although not nearly as good as those of an [[ostrich]].{{efn-ua|p. 186 and 190 in Mazzetta et al. (1998)<ref name="GVPaleobiology"/>}}<ref name="mazzetta1999"/> Scientists calculate that Carnotaurus had a top speed of up to {{convert|48|-|56|km|mi|abbr=on}} per hour.<ref>{{cite news|title=Predatory dinosaur was fearsomely fast|url=http://www.cbc.ca/news/technology/predatory-dinosaur-was-fearsomely-fast-1.1064092|access-date=April 22, 2017|work=[[CBC News]]|date=October 21, 2011|archive-date=December 22, 2020|archive-url=https://web.archive.org/web/20201222164224/https://www.cbc.ca/news/technology/predatory-dinosaur-was-fearsomely-fast-1.1064092|url-status=live}}</ref>

In dinosaurs, the most important locomotor muscle was located in the tail. This muscle, called the [[caudofemoralis]], attaches to the [[fourth trochanter]], a prominent ridge on the thigh bone, and pulls the thigh bone backwards when contracted. Scott Persons and [[Phil Currie]] (2011) argued that in the tail vertebrae of ''Carnotaurus'', the caudal ribs did not protrude horizontally ("T-shaped"), but were angled against the vertical axis of the vertebrae, forming a "V". This would have provided additional space for a caudofemoralis muscle larger than in any other theropod—the muscle mass was calculated at {{convert|111|to|137|kg}} per leg. Therefore, ''Carnotaurus'' could have been one of the fastest large theropods.<ref name="personscurrie2011"/> While the caudofemoralis muscle was enlarged, the [[epaxial and hypaxial muscles|epaxial muscles]] situated above the caudal ribs would have been proportionally smaller. These muscles, called the [[longissimus]] and [[spinalis]] muscle, were responsible for tail movement and stability. To maintain tail stability in spite of reduction of these muscles, the caudal ribs bear forward projecting processes interlocking the vertebrae with each other and with the pelvis, stiffening the tail. As a consequence, the ability to make tight turns would have been diminished, because the hip and tail had to be turned simultaneously, unlike in other theropods.<ref name="personscurrie2011"/>

===Brain and senses===
Cerroni and Paulina-Carabajal, in 2019, used a CT scan to study the endocranial cavity that contained the brain. The volume of the endocranial cavity was 168.8&nbsp;cm<sup>3</sup>, although the brain would only have filled a fraction of this space. The authors used two different brain size estimates, assuming a brain size of 50% and 37% of the endocranial cavity, respectively. This results in a [[Encephalization quotient|reptile encephalization quotient]] (a measure of intelligence) larger than that of the related ''Majungasaurus'' but smaller than in [[Tyrannosauridae|tyrannosaurids]]. The [[pineal gland]], which produces [[hormone]]s, might have been smaller than in other abelisaurids, as indicated by a low dural expansion – a space on top of the forebrain in which the pineal gland is thought to have been located.<ref name="Cerroni2019"/>

The [[olfactory bulb]]s, which housed the sense of smell, were large, while the [[Superior colliculus|optic lobes]], which were responsible for sight, were relatively small. This indicates that the sense of smell might have been better developed than the sense of sight, while the opposite is the case in modern birds. The front end of the olfactory tracts and bulbs were curved downwards, a feature only shared by ''[[Indosaurus]]''; in other abelisaurids, these structures were oriented horizontally. As hypothesized by Cerroni and Paulina-Carabajal, this downward-curvature, together with the large size of the bulbs, might indicate that ''Carnotaurus'' relied more on the sense of smell than other abelisaurids. The [[flocculus]], a brain lobe thought to be correlated with gaze stabilization (coordination between eyes and body), was large in ''Carnotaurus'' and other South American abelisaurids. This could indicate that these forms frequently used quick movements of the head and body. Hearing might have been poorly developed in ''Carnotaurus'' and other abelisaurids, as indicated by the short [[lagena (anatomy)|lagena]] of the [[inner ear]]. The hearing range was estimated to be below 3&nbsp;kHz.<ref name="Cerroni2019"/>

==Age and paleoenvironment==
[[File:Carnotaurus sastrei Andrey Atuchin.jpg|thumb|''Carnotaurus'' in environment]] 
Originally, the rocks in which ''Carnotaurus'' was found were assigned to the upper part of the [[Cerro Barcino Formation|Gorro Frigio Formation]], which was considered to be approximately 100 million years old ([[Albian]] or [[Cenomanian]] stage).<ref name="bonaparte1985"/>{{efn-ua|p. 3 in Bonaparte (1990)<ref name="bonaparte1990" />}} Later, they were realized to pertain to the much younger [[La Colonia Formation]],<ref name="bonaparte1996"/> dating to the [[Campanian]] and [[Maastrichtian]] stages (83.6 to 66 million years ago).<ref name="Cerroni2020"/> Novas, in a 2009 book, gave a narrower time span of 
72 to 69.9 million years ago (lower [[Maastrichtian]] stage).{{efn-ua|p. 276 in Novas (2009)<ref name="novas2009"/>}} ''Carnotaurus'' therefore was the latest South American abelisaurid known.<ref name="personscurrie2011"/> By the Late Cretaceous, South America was already isolated from both Africa and North America.<ref name="leloeuff1997"/>

The La Colonia Formation is exposed over the southern slope of the [[North Patagonian Massif]].<ref name="pascual2000"/> Most vertebrate fossils, including ''Carnotaurus'', come from the formation's middle section (called the ''middle facies association'').<ref name="pascual2000"/> This part likely represents the deposits of an environment of [[estuary|estuaries]], [[tidal flat]]s or [[coastal plain]]s.<ref name="pascual2000"/> The climate would have been seasonal with both dry and humid periods.<ref name="pascual2000"/> The most common vertebrates collected include [[Ceratodontidae|ceratodontid]] [[lungfish]], turtles, [[plesiosaur]]s, crocodiles, dinosaurs, lizards, snakes and mammals.<ref name="sterli2011"/> Other dinosaurs include ''[[Koleken|Koleken inakayali]]'', which is closely related to ''Carnotaurus'';<ref name="pol2024">{{cite journal |last1=Pol |first1=Diego |last2=Baiano |first2=Mattia Antonio |last3=Černý |first3=David |last4=Novas |first4=Fernando |last5=Cerda |first5=Ignacio A. |title=A new abelisaurid dinosaur from the end Cretaceous of Patagonia and evolutionary rates among the Ceratosauria |journal=  Cladistics|date=21 May 2024 |volume=40 |issue=3 |pages=307–356 |doi=10.1111/cla.12583 |doi-access=free |pmid=38771085 }}</ref> the [[Saltasauroidea|saltasauroid]] [[Titanosauria|titanosaur]] ''[[Titanomachya|Titanomachya gimenezi]]'';<ref>{{Cite journal|last1=Pérez-Moreno |first1=A. |last2=Salgado |first2=L. |last3=Carballido |first3=J. L. |last4=Otero |first4=A. |last5=Pol |first5=D. |year=2024 |title=A new titanosaur from the La Colonia Formation (Campanian-Maastrichtian), Chubut Province, Argentina |journal=Historical Biology: An International Journal of Paleobiology |pages=1–20 |doi=10.1080/08912963.2024.2332997 |doi-access=free}}</ref> an unnamed [[Ankylosauria|ankylosaur]]; and an unnamed [[Hadrosauroidea|hadrosauroid]], among others. Some of the snakes that have been found belong to the families [[Boidae]] and [[Madtsoiidae]], such as ''[[Alamitophis|Alamitophis argentinus]]''.<ref name="albino2000"/> Turtles are represented by at least five [[taxon|taxa]], four from [[Chelidae]] ([[Pleurodira]]) and one from [[Meiolaniidae]] ([[Cryptodira]]).<ref name="gasparinifuente2000"/> Plesiosaurs include two [[Elasmosauridae|elasmosaurs]] (''[[Kawanectes]]'' and ''[[Chubutinectes]]'') and a [[Polycotylidae|polycotylid]] (''[[Sulcusuchus]]'').<ref>{{Cite journal |last1=O’Gorman |first1=José P. |last2=Carignano |first2=Ana Paula |last3=Calvo-Marcilese |first3=Lydia |last4=Pérez Panera |first4=Juan Pablo |date=2023-08-10 |title=A new elasmosaurid (Sauropterygia, Plesiosauria) from the upper levels of the La Colonia Formation (upper Maastrichtian), Chubut Province, Argentina |journal=Cretaceous Research |volume=152 |language=en |pages=105674 |doi=10.1016/j.cretres.2023.105674 |bibcode=2023CrRes.15205674O |s2cid=260830333 |issn=0195-6671}}</ref><ref>{{cite journal | title = Revision of ''Sulcusuchus erraini'' (Sauropterygia, Polycotylidae) from the Upper Cretaceous of Patagonia, Argentina | first1 = J.P. | last1 = O'Gorman | journal = Alcheringa: An Australasian Journal of Palaeontology | last2 = Gasparini | first2 = Z. | volume = 37 | issue = 2 | date = 2013 | pages = 163–176 | doi = 10.1080/03115518.2013.736788 | bibcode = 2013Alch...37..163O | s2cid = 131429825 | hdl = 11336/2489 | hdl-access = free }}</ref> Mammals are represented by ''[[Reigitherium|Reigitherium bunodontum]]'' and ''[[Coloniatherium|Coloniatherium cilinskii]]'', the former of which was considered the first record of a South American [[Docodonta|docodont]],<ref name="pascual2000" /><ref>{{cite journal |last1=Rougier |first1=G. W. |last2=Turazzinni |first2=G. F. |last3=Cardozo |first3=M. S. |last4=Harper |first4=T. |last5=Lires |first5=A. I. |last6=Canessa |first6=L. A. |title=New Specimens of ''Reigitherium bunodontum'' from the Late Cretaceous La Colonia Formation, Patagonia, Argentina and Meridiolestidan Diversity in South America |journal=Journal of Mammalian Evolution |date=2021 |volume=28 |issue=4 |pages=1051–1081 |doi=10.1007/s10914-021-09585-2|s2cid=254704047 }}</ref> and the possible [[gondwanatheria]]ns or [[multituberculate]]s ''[[Argentodites|Argentodites coloniensis]]'' and ''[[Ferugliotherium|Ferugliotherium windhauseni]]''.<ref name=kielanjaworowska2007/><ref>{{Cite journal | last1 = Gurovich | first1 = Y. | last2 = Beck | first2 = R. | doi = 10.1007/s10914-008-9097-3 | title = The phylogenetic affinities of the enigmatic mammalian clade Gondwanatheria | journal = Journal of Mammalian Evolution | volume = 16| issue = 1| pages = 25–49 | year = 2009| s2cid = 42799370 }}</ref> Remains of an [[enantiornithine]] and, possibly, of a [[Neornithes|neornithine bird]] have been discovered.<ref name="lawver2011"/><ref>{{Cite journal|last1=Acosta Hospitaleche |first1=C. |last2=O'Gorman |first2=J. P. |last3=Panzeri |first3=K. M. |year=2023 |title=A new Cretaceous bird from the Maastrichtian La Colonia Formation (Patagonia, Argentina) |journal=Cretaceous Research |volume=150 |at=105595 |doi=10.1016/j.cretres.2023.105595 |bibcode=2023CrRes.15005595A |s2cid=259059084 }}</ref>

==See also==
{{Portal|Dinosaurs}}
* [[Timeline of ceratosaur research]]

==Notes==
{{Reflist|25em|group=upper-alpha}}

==References==
{{Reflist|40em|refs=
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<ref name="yong">{{cite journal |url=https://www.nationalgeographic.com/science/phenomena/2011/10/18/butch-tail-made-carnotaurus-a-champion-dinosaur-sprinter/ |archive-url=https://web.archive.org/web/20181029045945/https://www.nationalgeographic.com/science/phenomena/2011/10/18/butch-tail-made-carnotaurus-a-champion-dinosaur-sprinter/ |url-status=dead |archive-date=October 29, 2018 |first1=Ed |last1=Yong |journal=National Geographic |title=Butch tail made Carnotaurus a champion dinosaur sprinter |date=October 18, 2011 |access-date=July 31, 2019 }}</ref>
}}

==External links==
{{Commons category}}
*[https://web.archive.org/web/20080526041904/http://www.mdp.edu.ar/rectorado/secretarias/investigacion/nexos/16/16carnosaurio.htm The bite of ''Carnotaurus''] at Universidad Nacional de Mar del Plata. {{in lang|es}}
*[http://2.bp.blogspot.com/-mWCYzRbaCHs/T3R9p0CbcPI/AAAAAAAAICE/CDtOr0Z5vgY/s1600/carnotaurus.png Skeletal reconstruction by Scott Hartman]

{{Theropoda|B.|state=collapsed}}
{{Taxonbar|from=Q18510948}}
{{Authority control}}

[[Category:Abelisauridae]]
[[Category:Dinosaur genera]]
[[Category:Maastrichtian dinosaurs]]
[[Category:Fossil taxa described in 1985]]
[[Category:Taxa named by José Bonaparte]]
[[Category:Dinosaurs of Argentina]]