Bauria

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Bauria
Temporal range: Early - Middle Triassic, 251–246  Ma
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Bauria cynops 76thg.jpg
Skull of B. cynops
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Synapsida
Clade: Therapsida
Clade: Therocephalia
Family: Bauriidae
Subfamily: Bauriinae
Genus: Bauria
Broom 1909
Type species
Bauria cynops
Broom 1909
Other species

Bauria robustaHarksen, 1966

Bauria is an extinct genus of the suborder Therocephalia that existed during the Early and Middle Triassic period, around 246-251 million years ago. It belonged to the family Bauriidae. Bauria was probably a herbivore or omnivore.[ citation needed ] It lived in South Africa, specifically in the Burgersdorp Formation in South Africa. [1]

Contents

Taxonomy

Reconstruction of B. cynops skull specimen 5622 from 1915 Bauria.jpg
Reconstruction of B. cynops skull specimen 5622 from 1915

Bauria was named by Robert Broom in 1909 and found at Winnaarsbaken, South Africa. [2] The first species Broom discovered, Bauria cynops, was a reasonably complete skull, but according to the first description somewhat poorly preserved, and apparently equally poorly prepared. Five other specimens were later found at different points in time, with mostly skulls being found. [3]

There have only been two known species of Bauria that have been discovered so far, with the first species, Bauria cynops, being known from 6 different skulls in varying conditions of poor to excellent. [3]

The second species, Bauria robusta is known from a skull that is as much as twenty percent larger than the largest known specimen of Bauria cynops, which is about fifteen percent larger than the average of all other specimens of this genotype. [1] The skull was unfortunately not well preserved, due to exposure to weathering. [1] The only tangible evidence of a feature which is quite apparent to the eye is the fact that the snout appears to be stouter, higher and shorter than in Bauria cynops. [1] The cheek bulges in other Bauria specimens are below the anterior borders of the orbits, while in the new species they rise to a position more directly in front of the orbits. [1]

Only two species of Bauria are known, with the most recent one, Bauria robusta, being discovered by J. W. Kitching in 1955 in the Burghersdorp district [1] However, a 2013 study proposed that Microgomphodon oligocynus and Bauria cynops are recognized as the only valid species of southern African bauriids. [4]

B. cynops head restoration Bauria DB.jpg
B. cynops head restoration
Synapsida  

Caseasauria

  Sphenacodontia  

Sphenacodontidae

 Therapsida 

Based on Brink's analysis of skull and lower jaw features in 1963, Bauria is a therapsid sufficiently different from Scaloposaurus and its allies to warrant distinction at the infraorder level. [3] It was suggested that a suborder be recognized level with Gorgonopsia, Therocephalia, Cynodontia and Ictidosauria and that this suborder be called Scaloposauria. [3] The suborder Scaloposauria should be divided into two infraorders, the earlier Ictodosuchoidea and the later Bauriamorpha, a natural branch separate from the suborder Cynodontia. [3]

Bauria was later confirmed to be a sister taxon of cynodonts, followed by an outgroup formed by (Moschorhinus (Ictidosuchops, Theriognathus)), using techniques involving Most Parsimonious Trees. [5]

Most therocephalian genera lack an ectepicondylar foramen, with Bauria being the only exception, making Bauria a derived genera. [6]

Description

Size of B. cynops compared to a human Restoration Bauria NT.jpg
Size of B. cynops compared to a human Restoration

Skull

According to what Brink compiled, the basioccipital of Bauria contributes in the typical therocephalian-scaloposaurid manner to the occipital condyle. [3] In Bauria, the three exoccipitals are of equal size. [3] The shape of the rest of the basioccipital in ventral view doesn't differ too much from other related forms like Ictidosuchops. [3] The opisthotic contribution is visible in ventral view. [3] There is the presence of bosses on the exoccipitals, dorsally and laterally, which mark the areas of articulation of the proatlas. [3] The parietals form a parietal crest, in contrast with the slightly broader, more rounded ictidosuchoid condition. [3] The fronto-parietal suture is narrow in Bauria, which differs from ictidosuchids who have a generally broader region [7] The pineal foramen is absent, a feature of considerable significance at this critical level near the threshold of homoiotherm mammals. [3] The postorbitals are very characteristic, making it possible to identify Bauria on one isolated postorbital bone. [3] The posterior extensions flanking the parietals do not extend upward, the postorbital frontal sutures form no ridges, unlike in ictidosuchoids. [3]

B. cynops skull from above Bauria-cynops 56ty.jpg
B. cynops skull from above

The dentary is peculiarly curved, making it a characteristic of this genus. [3] The peculiar twist is designed to swing the posterior lower cheek teeth inward to ensure proper occlusion on the upper teeth. [3] The dentary is greatly thickened, both internally and externally along the series of cheek teeth, much more than the transversely broadened teeth and their roots demand. [3] The posterior part of the dental row is displaced inward so the dorsal margin of the coronoid process descends some distance laterally to the hindmost teeth and continues down and forward across the lateral face of the dentary virtually to the chin. [3] This arrangement gives the dentary a very mammal-like or ictidosaur appearance, but the coronoid process is by contrast typically scaloposaurid. [3] It reaches far back and high through the temporal vacuity, but as a long slender extension, somewhat square terminally. [3] There are three large incisors, one short canine only slightly larger than the incisors, and it would appear that the cheek teeth normally count one more than in the upper jaw. [3] The lower teeth are narrower than the upper teeth, but are still distinctly transversely ovate. [3] All the teeth in the series are twice as wide as their antero-posterior measurement. [3] The therocephalian Bauria shows a more complex postcanine crown pattern, but only one cusp can be seen in labial view [8] [9]

Palaeobiology

Life restoration showing B. cynops without fur Bauria BW.jpg
Life restoration showing B. cynops without fur

The diet of Bauria is assumed to have included tough fibrous material due to the way the anterior edge of an upper tooth shears against the posterior edge of the corresponding lower tooth to generate a cutting action. [10]

The cheek bulges, and the wide and deep depression below them, suggest a muscular arrangement associated with the corners of the mouth, whereby it is possible for such an animal to pull the corners of the mouth forwards as is characteristic of mammals, while in true reptiles the corners of the mouth are fixed and very close to the articulation of the lower jaw. [1] This is a significant arrangement, because even with a secondary palate an animal would not be able to suck unless the corners of the mouth can be brought forward, allowing the mouth as a whole to close properly around the teat of a milk gland. [1]

See also

Related Research Articles

<span class="mw-page-title-main">Therapsida</span> Clade of tetrapods including mammals

Therapsida is a clade composing of 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, as opposed to the sprawling posture of many reptiles and salamanders.

<span class="mw-page-title-main">Cynodontia</span> Clade of therapsids

Cynodontia is a clade of eutheriodont therapsids that first appeared in the Late Permian, and extensively diversified after the Permian–Triassic extinction event. Mammals are cynodonts, as are their extinct ancestors and close relatives (Mammaliaformes), having evolved from advanced probainognathian cynodonts during the Late Triassic.

<i>Ericiolacerta</i> Extinct genus of therapsid from the early Triassic

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.

<span class="mw-page-title-main">Therocephalia</span> Extinct order of therapsids

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.

<span class="mw-page-title-main">Theriodontia</span> Clade of therapsids

The theriodonts are a major group of therapsids which appeared during the Middle Permian and which includes the gorgonopsians and the eutheriodonts, itself including the therocephalians and the cynodonts.

<i>Moschorhinus</i> Genus of synapsid from late Permian and early Triassic South Africa

Moschorhinus is an extinct genus of therocephalian synapsid in the family Akidnognathidae with only one species: M. kitchingi, which has been found in the Late Permian to Early Triassic of the South African Karoo Supergroup. It was a large carnivorous therapsid, reaching 1.5 m (4.9 ft) in total body length with the largest skull comparable to that of a lion in size, and had a broad, blunt snout which bore long, straight canines.

<i>Theriognathus</i> Extinct genus of therapsids from late Permian South Africa and Tanzania

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.

<i>Scylacops</i> Extinct genus of therapsids

Scylacops is an extinct genus of Gorgonopsia. It was first named by Broom in 1913, and contains two species, S. bigendens, and S. capensis. Its fossils have been found in South Africa and Zambia. It is believed to be closely related to the Gorgonopsian Sauroctonus progressus. Scylacops was a moderately sized Gorgonopsid.

Cynosaurus is an extinct genus of cynodonts. Remains have been found from the Dicynodon Assemblage Zone in South Africa. Cynosaurus was first described by Richard Owen in 1876 as Cynosuchus suppostus. Cynosaurus has been found in the late Permian period. Cyno- is derived from the Greek word kyon for dog and –sauros in Greek meaning lizard.

<i>Glanosuchus</i> Extinct genus of therapsids

Glanosuchus is a genus of scylacosaurid therocephalian from the Late Permian of South Africa. The type species G. macrops was named by Robert Broom in 1904. Glanosuchus had a middle ear structure that was intermediate between that of early therapsids and mammals. Ridges in the nasal cavity of Glanosuchus suggest it had an at least partially endothermic metabolism similar to modern mammals.

<i>Microgomphodon</i> Genus of therapsid from the Middle Triassic of southern Africa

Microgomphodon is an extinct genus of therocephalian therapsid from the Middle Triassic of South Africa and Namibia. Currently only one species of Microgomphodon, M. oligocynus, is recognized. With fossils present in the Cynognathus Assemblage Zone (CAZ) of the Burgersdorp Formation in South Africa and Omingonde Formation of Namibia and ranging in age from late Olenekian to Anisian, it is one of the most geographically and temporally widespread therocephalian species. Moreover, its occurrence in the upper Omigonde Formation of Namibia makes Microgomphodon the latest-surviving therocephalian. Microgomphodon is a member of the family Bauriidae and a close relative of Bauria, another South African bauriid from the CAZ. Like other bauriids, it possesses several mammal-like features such as a secondary palate and broad, molar-like postcanine teeth, all of which evolved independently from mammals.

Platycraniellus is an extinct genus of carnivorous cynodonts from the Early Triassic. It is known from the Lystrosaurus Assemblage Zone of the Normandien Formation in South Africa. P. elegans is the only species in this genus based on the holotype specimen from the Ditsong National Museum of Natural History in Pretoria, South Africa. Due to limited fossil records for study, Platycraniellus has only been briefly described a handful of times.

<i>Scymnosaurus</i> Extinct genus of therapsids from middle Permian South Africa

Scymnosaurus is a dubious genus of therocephalian therapsids based upon various fossils of large early therocephalians. The genus was described by Robert Broom in 1903 with S. ferox, followed by S. watsoni in 1915 and a third, S. major, by Lieuwe Dirk Boonstra in 1954. Each of these species are considered nomen dubia today and based upon specimens belonging to two separate families of therocephalians. S. ferox and S. major represent specimens of Lycosuchidae incertae sedis, while S. watsoni is Scylacosauridae incertae sedis. Broom named a fourth species in 1907 from KwaZulu-Natal, S. warreni, though he later referred it to Moschorhinus as a valid species in 1932 but now is recognised as being synonymous with M. kitchingi.

<span class="mw-page-title-main">Bauriidae</span> Extinct family of therapsids

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.

<i>Blattoidealestes</i> Extinct genus of therapsid from Middle-Permian South Africa

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.

Homodontosaurus is an extinct genus of therocephalian therapsids from the Late Permian of South Africa. The type species Homodontosaurus kitchingi was named by South African paleontologist Robert Broom in 1949. Broom based his description on a small skull found in the Cistecephalus Assemblage Zone near Graaff-Reinet. The skull is very small, at about 55 millimetres (2.2 in) long and 20 millimetres (0.79 in) wide. Homodontosaurus has large eye sockets and an elongated snout. The lower jaw is long, thin, and curved. Numerous small teeth line the upper jaw and are long, pointed, and round in cross-section.

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.

Pelictosuchus is an extinct genus of therocephalian therapsids from the Late Permian of South Africa. It is classified in the family Akidnognathidae. The type species Pelictosuchus paucidens was named by South African paleontologist Robert Broom in 1940 from the Dicynodon Assemblage Zone.

Vetusodon is an extinct genus of cynodonts belonging to the clade Epicynodontia. It contains one species, Vetusodon elikhulu, which is known from four specimens found in the Late Permian Daptocephalus Assemblage Zone of South Africa. With a skull length of about 18 centimetres (7.1 in), Vetusodon is the largest known cynodont from the Permian. Through convergent evolution, it possessed several unusual features reminiscent of the contemporary therocephalian Moschorhinus, including broad, robust jaws, large incisors and canines, and small, single-cusped postcanine teeth.

References

  1. 1 2 3 4 5 6 7 8 Brink, A.S. (1965). "A New Large Bauriamorph From the Cynognathus-Zone of South Africa".{{cite journal}}: Cite journal requires |journal= (help)
  2. Schaeffer, Bobb. (1941). ""The Pes of Bauria cynops Broom."".{{cite journal}}: Cite journal requires |journal= (help)
  3. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 Brink, A.S. (1963). "On Bauria cynops Broom".{{cite journal}}: Cite journal requires |journal= (help)
  4. Fernando et al. "New Material of Microgomphodon oligocynus (Eutherapsida, Therocephalia) and the Taxonomy of Southern African Bauriidae" (2013).
  5. Abdala, Fernando. "Redescritpion of Platycraniellus elegans (Therapsida, Cynodontia) from the Lower Triassic of South Africa, and the Cladistic Relationships of Eutheriodonts." (2007).
  6. King, G.M. "A description of the skeleton of a bauriid therocepahalian from the early Triassic of South Africa." Annals of the South African Museum (1996).
  7. Brink, A.S. "A New Ictidosuchid (Scaloposauria) From the Lystrosaurus-Zone." (1965).
  8. Botha et al. "The oldest cynodont: new clues on the origin and early diversification of the Cynodontia." Zoological Journal of the Linnean Society (2007).
  9. Crompton, AW. "On the dentition and tooth replacement in two bauriamorph reptiles." Annals of South African Museum (1962).
  10. Kemp, T.S. (2005). "The Origin and Evolution of Mammals.".{{cite journal}}: Cite journal requires |journal= (help)