Baurioidea Temporal range: Late Permian - Middle Triassic | |
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Life restoration of Regisaurus jacobi | |
Scientific classification ![]() | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Synapsida |
Clade: | Therapsida |
Clade: | † Therocephalia |
Clade: | † Eutherocephalia |
Superfamily: | † Baurioidea Broom, 1911 |
Genera | |
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Synonyms | |
Baurioidea is a superfamily of therocephalian therapsids. It includes advanced therocephalians such as Regisaurus and Bauria . [2] The superfamily was named by South African paleontologist Robert Broom in 1911. Bauriamorpha, named by D. M. S. Watson and Alfred Romer in 1956, is a junior synonym of Baurioidea.
Many baurioids were once placed in a group called Scaloposauria. Scaloposaurs were characterized by their small size and reduced postorbital bar (a strut of bone behind the eye socket). Scaloposauria is no longer recognized as a valid taxon because it likely represents juvenile forms of many groups of therocephalians. Most scaloposaurs, including Scaloposaurus and Regisaurus, are now classified in various positions within Bauroidea. [3]
Many therocephalians once classified as scaloposaurians are now considered basal baurioids. The classification of these species is uncertain, as there have been no comprehensive phylogenetic analyses of scaloposaurian taxa. The validity of many of these species is questionable, as future studies may find some to be synonymous. [4] Below is a list of these taxa:
Therapsida is a clade comprising a major group of eupelycosaurian synapsids that includes mammals and their ancestors and close relatives. Many of the traits today seen as unique to mammals had their origin within early therapsids, including limbs that were oriented more underneath the body, resulting in a more "standing" quadrupedal posture, as opposed to the lower sprawling posture of many reptiles and amphibians.
Ericiolacerta is an extinct genus of small therocephalian therapsids from the early Triassic of South Africa and Antarctica. Ericiolacerta, meaning "hedgehog lizard", was named by D.M.S. Watson in 1931. The species E. parva is known from the holotype specimen which consists of a nearly complete skeleton found in the Lystrosaurus Assemblage Zone within the Katberg Formation of the Beaufort Group in South Africa, and from a partial jaw found in the Lower Triassic Fremouw Formation in Antarctica. Ericiolacerta was around 20 centimetres (7.9 in) in length, with long limbs and relatively small teeth. It probably ate insects and other small invertebrates. The therocephalians – therapsids with mammal-like heads – were abundant in Permian times, but only a few made it into the Triassic. Ericiolacerta was one of those. It is possible that they gave rise to the cynodonts, the only therapsid group to survive into post-Triassic times. Cynodonts gave rise to mammals.
Therocephalia is an extinct clade of eutheriodont therapsids from the Permian and Triassic periods. The therocephalians ("beast-heads") are named after their large skulls, which, along with the structure of their teeth, suggest that they were carnivores. Like other non-mammalian synapsids, therocephalians were once described as "mammal-like reptiles". Therocephalia is the group most closely related to the cynodonts, which gave rise to the mammals, and this relationship takes evidence in a variety of skeletal features. Indeed, it had been proposed that cynodonts may have evolved from therocephalians and so that therocephalians as recognised are paraphyletic in relation to cynodonts.
Theriognathus is an extinct genus of therocephalian therapsid belonging to the family Whaitsiidae, known from fossils from South Africa, Zambia, and Tanzania. Theriognathus has been dated as existing during the Late Permian. Although Theriognathus means mammal jaw, the lower jaw is actually made up of several bones as seen in modern reptiles, in contrast to mammals. Theriognathus displayed many different reptilian and mammalian characteristics. For example, Theriognathus had canine teeth like mammals, and a secondary palate, multiple bones in the mandible, and a typical reptilian jaw joint, all characteristics of reptiles. It is speculated that Theriognathus was either carnivorous or omnivorous based on its teeth, and was suited to hunting small prey in undergrowth. This synapsid adopted a sleek profile of a mammalian predator, with a narrow snout and around 1 meter long. Theriognathus is represented by 56 specimens in the fossil record.
Moschowhaitsia is an extinct genus of therocephalian therapsids from the Late Permian (Guadalupian) of Russia and China. The type species, Moschowhaitsia vjuschkovi, was discovered in the Changxingian-aged Archosaurus Assemblage Zone of Russia and named in 1963 by Russian palaeontologist Leonid Petrovich Tatarinov. A second species was discovered in Jingtai County of Gansu, China in 2020 and named as M. lidaqingi in 2023 by Jun Liu and Fernando Abdala, the first whaitsiid therocephalian to be discovered in China. It was among the larger carnivores in the faunal assemblages it occurred in, with a skull-length of up to 25 centimetres (9.8 in) in M. vjuschkovi and an even larger estimated 35 centimetres (14 in) for M. lidaqingi, one of the largest therocephalian skulls reported. The genus name Moschowhaitsia alludes to two other therocephalians, Moschorhinus and Whaitsia, due to the structure of its palate combining physical features of both these genera.
Tetracynodon is an extinct genus of therocephalian. Fossils of Tetracynodon have been found in the Karoo Basin of South Africa. Two species are known: the type species T. tenuis from the Late Permian and the species T. darti from the Early Triassic. Both species were small-bodied and probably fed on insects and small vertebrates. Although Tetracynodon is more closely related to mammals than to reptiles, its braincase is very primitive and more resembles that of modern amphibians and reptiles than of mammals.
Akidnognathidae is an extinct family of therocephalian therapsids from the Late Permian and Early Triassic of South Africa, Russia and China. The family includes many large-bodied therocephalians that were probably carnivorous, including Moschorhinus and Olivierosuchus. One akidnognathid, Euchambersia, may even have been venomous. Akidnognathids have robust skulls with a pair of large caniniform teeth in their upper jaws. The family is morphologically intermediate between the more basal therocephalian group Scylacosauridae and the more derived group Baurioidea.
Bauriidae is an extinct family of therocephalian therapsids. Bauriids were the latest-surviving group of therocephalians after the Permian–Triassic extinction event, going extinct in the Middle Triassic. They are among the most advanced eutherocephalians and possess several mammal-like features such as a secondary palate and wide postcanine teeth at the back of the jaws. Unlike other therocephalians, bauriids were herbivorous. They were also smaller than earlier members of the group. Two subfamilies are classified within Bauriidae: Nothogomphodontinae and Bauriinae.
Choerosaurus is an extinct genus of therocephalian therapsids from the Late Permian of South Africa. The type species Choerosaurus dejageri was named by South African paleontologist Sidney H. Haughton from the Tropidostoma Assemblage Zone in 1929.
Blattoidealestes is an extinct genus of therocephalian therapsid from the Middle Permian of South Africa. The type species Blattoidealestes gracilis was named by South African paleontologist Lieuwe Dirk Boonstra from the Tapinocephalus Assemblage Zone in 1954. Dating back to the Middle Permian, Blattoidealestes is one of the oldest therocephalians. It is similar in appearance to the small therocephalian Perplexisaurus from Russia, and may be closely related.
Icticephalus is an extinct genus of therocephalian therapsids from the Middle and Late Permian of South Africa. The type species Icticephalus polycynodon was named from the Tapinocephalus Assemblage Zone by South African paleontologist Robert Broom in 1915. Specimens of Icticephalus have also been described from the Cistecephalus Assemblage Zone. Broom originally placed Icticephalus in the Scaloposauridae, a group of very small therocephalians. Most scaloposaurids are now thought to be juvenile forms of other therocephalians, and Scaloposauridae is no longer recognized as a valid grouping. Icticephalus and other former scaloposaurids are now classified as basal members of Baurioidea.
Silpholestes is an extinct genus of therocephalian therapsids from the Late Permian of South Africa. The type species Silpholestes jackae was named by South African paleontologist Robert Broom in 1948 from the Cistecephalus Assemblage Zone.
Ictidodraco is an extinct genus of therocephalian therapsids from the Late Permian of South Africa. The type species Ictidodraco longiceps was named by South African paleontologists Robert Broom and John T. Robinson in 1948 from the Cistecephalus Assemblage Zone. Ictidodraco was once classified as a scaloposaurian in the family Silpholestidae. Scaloposauria and Silpholestidae are no longer regarded as valid groups, and Ictidodraco is now classified as a basal member of the clade Baurioidea.
Scalopodon is an extinct genus of therocephalian therapsids from the Late Permian of Russia. The type species Scalopodon tenuisfrons was named in 1999 from the Kotelnichsky District of Kirov Oblast. Scalopodon is known from a single fragmentary holotype specimen including the back of the skull, the left side of the lower jaw and isolated postorbital and prefrontal bones. The skull was found in the Deltavjatia Assemblage Zone, which dates back to the early Wuchiapingian about 260 million years ago. Distinguishing features of Scalopodon include narrow frontal bones and a distinctive sagittal crest along the parietal region at the back of the skull. Scalopodon was originally classified in the family Scaloposauridae, and was the first scaloposaurid found in Russia. More recent studies of therocephalians have found scaloposaurids like Scalopodon to be juvenile forms of larger therocephalians and do not consider Scaloposauridae to be a valid group. Scalopodon and most other scaloposaurids are now classified as basal members of Baurioidea.
Macroscelesaurus is an extinct genus of therocephalian therapsid from the Late Permian of South Africa. The type species Macroscelesaurus janseni was named by Sidney H. Haughton in 1918 from the Cistecephalus Assemblage Zone. It is one of the few therocephalians known from postcranial remains.
Polycynodon is an extinct genus of therocephalians from the Late Permian of South Africa. It is known from the Cistecephalus Assemblage Zone. The type species was first described as Octocynodon elegans by South African paleontologist Robert Broom in 1940, but the name Octocynodon was preoccupied by a genus of labrid fish first described in 1904. Along with John T. Robinson, Broom instated Polycynodon as a replacement name for O. elegans in 1948. Polycynodon is classified in Baurioidea, although its relationship to other baurioid therocephalians is uncertain.
Lycideops is an extinct genus of therocephalians from the Late Permian of South Africa. The type species is Lycideops longiceps, named in 1931 by South African paleontologist Robert Broom. Fossils of Lycideops come from the Dicynodon Assemblage Zone of the Beaufort Group. Lycideops is a member of the family Lycideopidae. Like other lycideopids, Lycideops has a long snout.
Urumchia is an extinct genus of therocephalian therapsids from the Early Triassic of China. The type species Urumchia lii was described by Chinese paleontologist C. C. Young in 1952 from the Jiucaiyuan Formation in Xinjiang. The holotype skull has been lost, but Young was able to describe the species on the basis of a detailed cast of the skull. Urumchia is similar to the South African therocephalian Regisaurus in having an expanded pair of vomer bones on the underside of the skull that form a secondary palate. In Urumchia the front end of the vomers narrow to a point, while in Regisaurus they do not. Urumchia has six incisors on either side of the upper jaw, a primitive condition among baurioid therocephalians that usually have fewer incisors.
Yikezhaogia is an extinct genus of therocephalian therapsids from the Early Triassic of Inner Mongolia (China). It is known from a single fragmentary skull and associated postcranial bones representing the species Yikezhaogia megafenestrala. It is identifiable as a therocephalian by its thin postorbital bar behind the eye socket, its elongated temporal opening behind the bar, and a thin lower jaw with a low coronoid process. Large tooth sockets in the upper jaw indicate that Yikezhaogia had large caniniform teeth. The teeth of the lower jaw are blunt-tipped and cylindrical. Although its exact position among therocephalians is uncertain, Yikezhaogia is probably a basal member of the group Baurioidea.
Simorhinella is an extinct genus of therocephalian therapsids from the Late Permian of South Africa. It is known from a single species, Simorhinella baini, named by South African paleontologist Robert Broom in 1915. Broom named it on the basis of a single fossil collected by the British Museum of Natural History in 1878 that included the skull and jaws forward from the eye sockets. The skull is unusual in that it has an extremely short and deep snout, unlike the longer and lower snouts of most other therocephalians. Because of the skull's distinctiveness, the classification of Simorhinella within Therocephalia is uncertain. However, a 2014 study proposed that it was closely related to the basal therocephalian Lycosuchus, placing it in the family Lycosuchidae.