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Austroraptor ( ) is a of that lived during the and ages of the period in what is now .

Austroraptor was a large, moderately-built, ground-dwelling, , measuring around long and weighing up to . It is one of the largest paravians known, with only large dromaeosaurids such as and approaching a similar size.


Discovery and naming
The type specimen of Austroraptor cabazai, MML-195, was recovered in the Bajo de Santa Rosa locality of the , in Río Negro, . The specimen was collected in 2002 by the team of Fernando Emilio Novas of the Museo Argentino de Ciencias Naturales. It consists of a fragmentary skeleton including parts of the skull, lower jaw, a few neck and torso vertebrae, some ribs, a humerus, and assorted bones from both legs. The specimen was prepared by Marcelo Pablo Isasi and Santiago Reuil. In 2008, the Austroraptor cabazai was named and described by Fernando Emilio Novas, Diego Pol, Juan Canale, Juan Porfiri and Jorge Calvo. The genus name Austroraptor means "Southern Thief," and is derived from the word auster meaning "the south wind" and the word raptor meaning "thief." The specific name cabazai was chosen in honor of Héctor "Tito" Cabaza, who founded the Museo Municipal de Lamarque where the specimen was partially studied.

In 2012, and Ariana Paulina-Carabajal referred a second specimen to Austroraptor cabazai, MML-220, that was found in 2008. This specimen, a partial skeleton with the skull of an adult individual slightly smaller than the holotype, is also housed in the collection of the Museo Municipal de Lamarque in Argentina. It complements the holotype in several elements, mainly the lower arm, hand and foot.


Description
It is the largest to be discovered in the Southern Hemisphere; Novas et al. estimated that Austroraptor measured in length from head to tail and weighed . Gregory S. Paul later estimated its length at and weight of . In 2014, Benson and colleagues estimated that Austroraptor weighed up to . Supporting Information

The skull is low and elongated, much more so than that of other dromaeosaurs, and measures . Austroraptor has conical, non-serrated teeth, which Novas et al. compared to those of , based on how the of the surface of its teeth is fluted. Austroraptor shares a trait that is unique to it and to : the descending process of the curves anteriorly to a large degree. Austroraptor has a bizarre morphology in its , which are strangely disproportionate. The 4th toe is over twice the width of the 2nd toe, and nearly three times the expected width based on similarly sized members of its taxonomic family. This has suggested to some researchers that the holotype specimen is a paleontological chimera; however, there is no uncertainty about the affinity of the taxon, so a chimera hypothesis can not be assured.

Several of Austroraptor's skull bones bear some resemblance to those of the smaller . The front limbs of Austroraptor were short for a dromaeosaur, with its less than half the length of its . Among the Dromaeosauridae, only this genus, , and Mahakala have similarly reduced forelimbs. The relative length of its arms has caused Austroraptor to be compared to another, more famous short-armed dinosaur, , though there is no close relationship between the two taxa.


Distinguishing traits
However little of the entire skeleton was found, the bones that are available for analysis possess some distinct characteristics that differentiate Austroraptor from other dromaeosaurs. Austroraptor is particularly notable because of its relatively short forearms, which are much shorter in proportion when compared to the majority of the members of Dromaeosauridae. According to Novas et al. 2008, Austroraptor can be distinguished based on the following characteristics:
  • A lacrimal that is highly pneumatized, with the descending process strongly curved rostrally, and with a caudal process flaring out horizontally above the orbit.
  • The lack of a dorsomedial process on the postorbital bone for articulation with the frontal bone, and with the squamosal process extremely reduced.
  • The maxillary and dentary teeth are small, conical, devoid of serrations and fluted.
  • The humerus is short, at approximately 46% of length of the femur.
  • The pedal phalanx II-2 is transversely narrow, contrasting with the extremely robust phalanx IV-2.

In 2012, comparison with a second specimen showed that the fourth toe was not especially broad; the purported second phalanx had in fact been a first phalanx.


Classification
A analysis of the holotype specimen's anatomical features by the describers placed Austroraptor within the subfamily of Dromaeosauridae. This assignment was based on characteristics observed in the bones of the skull, the teeth, and the geometry and formation of the specimen's vertebral elements. It was determined that Austroraptor was a close relative of the unenlagiine dromaeosaur , with which it shares certain derived characteristics of the neck vertebrae.

The following is based on the phylogenetic analysis conducted by Turner, Makovicky and Norell in 2012, showing the relationships of Austroraptor among the other genera assigned to the taxon :

Cau et al. 2017 published a phylogenetic analysis of the Dromaeosauridae during the description of , in which members of the Unenlagiinae are classified as:

In 2019, during the description of Hesperornithoides, many groups were examined for the inclusion of the new . In this analysis, Austroraptor is found to be a more basal member of Unenlagiinae.

In 2021, Brum and colleagues classified as a to Austroraptor.


Paleobiology
It has been suggested that unenlagiines had better capacities for running and pursuit predation than other dromaeosaurids. While dromaeosaurids () were more stocky and had shorter legs and had an active predatory lifestyle, unenlagiines could likely maintain high speeds for extended amounts of time because they were more gracile. Unenlagiines have modified metatarsals that resemble those of : they are relatively thin and lengthened. Based on these adaptations, it is likely that unenlagiines preyed on small, fast animals, although the exact animals are unknown. features particular traits that can be attributed to specific hunting methods.

Models for Buitreraptor propose that it hunted by traveling large distances in pursuit of prey, which may explain the long-legged trait shared by various genera of Unenlagiidae. Buitreraptor is characterized by its long forelimbs and hands; it likely relied on them to restrain prey and the curved claw of the second pedal digit would have injured or killed the victim. Buitreraptor probably swallowed its prey whole due to its lack of serrated teeth with flesh-tearing capabilities; the teeth functioned to simply hold prey.

The same model was proposed for the much larger Austroraptor with few exceptions:

  • It would not have used its arms to handle prey, due to their relatively small size.
  • Its teeth were conical and probably stronger, so it may have been able to use them for hunting larger prey.

The teeth of Austroraptor are conical and lacking denticles, similarly to those of . Since it probably had a subarctometatarsal condition and similar hindlimb lengths compared to Buitreraptor, Austroraptor likely had well-developed capacities. In 2021, Brum and colleagues suggested that unenlagiines such as Austroraptor and its sister taxon Ypupiara likely consumed fish for a considerable part of their diet, possibly even as a main food source, based on their non-serrated conical teeth that are similar to those of piscivorous tetrapods including , , , etc.


Paleoecology
The holotype specimen was found in terrestrial sediments that were deposited during the stage of the period. Thomas R. Holtz Jr. has estimated that Austroraptor lived between 78 million and 66 million years ago, until the end of the era. Supplementary Information 2012 Austroraptor shared its paleoenvironment in the with diverse and early mammals. The discovery of Austroraptor increases the understanding of ecological and morphological diversity among unenlagiines, demonstrating that members of the subfamily included giant short-armed and small long-armed members, and suggesting that during the end of the Cretaceous large became common after the decreasing dominance of carcharodontosaurids. This genus represents the earliest record of dromaeosaurids, and supports the fact that large dromaeosaurids took the role of large alongside such as , and .

During his description of , Salgado suggested that large and inhabited interior environments of the region, and contemporaneous and the titanosaur inhabited coastal lowlands. The diversity among titanosaurs indicates that the had environments that supported a great range of dinosaurs. Other contemporaneous includes the titanosaurs , and , the , and the hadrosaurids , , and .


See also


Notes

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