Burnetia

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Burnetia
Temporal range: Late Permian
Burnetia mirabilisDB.jpg
Life restoration of Burnetia mirabilis
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Synapsida
Clade: Therapsida
Suborder: Biarmosuchia
Family: Burnetiidae
Genus: Burnetia
Broom, 1923
Species:
B. mirabilis
Binomial name
Burnetia mirabilis
Broom, 1923

Burnetia is an extinct genus of biarmosuchian therapsids in the family Burnetiidae, from the Late Permian of South Africa. Burnetia is known so far from a single holotype skull lacking the lower jaws described by South African paleontologist Robert Broom in 1923. Due to erosion and dorsoventral crushing, features of the skull are hard to interpret. Stutural lines are further distorted by the unusual shape of the skull roof, including many bosses and protuberances. [1]

Contents

Description

When broadly looking at the skull, there are well-developed "cheeks", bosses and pits that resemble Pareiasaurians'. However, the small temporal fossa distinguishes it from the Cotylosaur. [2] The overall shape resembles a triangle. [3] In the nasals, there is a bulging expansion of bone. Unlike proburnetia's median nasal bridge being long, narrow and raised, Burnetia's is splindle-shaped. [4] The median nasal boss is spindle-shaped. The snout is wide and blunt. The large preorbital pits on the lachrymal are significant. [2] Over the orbit there are notable ridges on the prefrontal and frontal. The supra-orbital ridges make the orbits face distally and posteriorly. [2] The suborbital eminence is subdivided into distinguished portions. [4] The small pineal foramen sits dorsally on a boss. [4]

Burnetia's palate is similar to Gorgonopsians'. Anteriorly, the internal nares have the lower canines. The maxilla is adjacent to the palatine, and posterior to the palatine is the long prevomer that meets the premaxilla. The palatine is tooth bearing, as well as the pterygoid that is just posterior to the palatine. [2] The vomer is held by the surrounding vomerine processes that form the choanae's middle border. [1] Unlike the rest of burnetiamorphs, Burnetia's interchoanal part of the vomer is not narrow. [4]

The concave occiput is tilted up, which is shown when it is aligned vertically, the snout faces downward. [1] The supraoccipital sits anterior to the paraoccipital. The size of the basioccipital is considered to be small. The majority of the occipital surface, posterior "horn", and posterior lateral margins are made from the squamosal. [1]

The basisphenoid in Burnetia differs from Gorgonopsians'. In Burnetia, their basisphenoid is round and shallow. In the middle of the basisphenoid, it is separated by a groove. Gorgonopsians' basisphenoid contrasts Burnetia's by having a "single sharp median keel". [2]

Discovery

Broom found Burnetia mirabilis in the Dicynodon Assemblage Zone near Graaff-Reinet, South Africa. [1] Broom concluded that Burnetia was related closest to the group of Gorgonopsians. [1] However, Broom made observations based on the skull when it was covered by matrix and no underlying bone was visible. [2] Lieuwe Boonstra removed this matrix and found that Burnetia and Gorgonopsians differed mainly by the thickening of dermal bones, bosses and their basisphenoids. [2]

Paleoenvironment

Phylogenetic analysis done by Ashley Kruger suggests that a likely origin for burnetiamorphs could be southern Africa. The base and oldest burnetiamorphs are found in South Africa. [5]

The family Burnetiidae came from the discovery of Burnetia, but new discoveries led to the studies of burnetiamorphs. [5] Burnetiamorphs only have about two taxa that represent each genus. It was previously believed that the Burnetiidae clade only contained two taxa, Burnetia mirabilis and Proburnetia viatkensis, but later Pachydectes and Bullacephalus were found to be included in the clade, as well. [1] [6] It was unable to be confirmed if Pachydectes shared the feature of nasal the nasal supporting a middle boss like Burnetia. However, like Burnetia, above the postorbital bar they have a significant boss. [6] Lycaenodon longiceps is in the clade Biarmosuchia and has some similarities to Burnetia. [7] Both Lycaenodon and Burnetia likely had a large foramen, surrounded by the vomer and vomerine process. This foramen implies that in biarmosuchians, the vomeronasal organ may have communicated with the oral cavity. They also share the trait of having a long vomerine process. [7] The first burnetiid therapsid found in Tanzania's Usili Formation was found to most resemble Burnetia. The Usili burnetiid and Burnetia both had bosses above their orbits that were "S"-like. [8]

Related Research Articles

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

A therapsid is a member of the clade Therapsida which is a major group of eupelycosaurian synapsids that includes mammals and their ancestors and 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">Biarmosuchia</span> Extinct suborder of therapsids

Biarmosuchia is an extinct clade of non-mammalian synapsids from the Permian. Biarmosuchians are the most basal group of the therapsids. They were moderately-sized, lightly built carnivores, intermediate in form between basal sphenacodont "pelycosaurs" and more advanced therapsids. Biarmosuchians were rare components of Permian ecosystems, and the majority of species belong to the clade Burnetiamorpha, which are characterized by elaborate cranial ornamentation.

<i>Tapinocephalus</i> Assemblage Zone

The Tapinocephalus Assemblage Zone is a tetrapod assemblage zone or biozone which correlates to the middle Abrahamskraal Formation, Adelaide Subgroup of the Beaufort Group, a fossiliferous and geologically important geological Group of the Karoo Supergroup in South Africa. The thickest outcrops, reaching approximately 2,000 metres (6,600 ft), occur from Merweville and Leeu-Gamka in its southernmost exposures, from Sutherland through to Beaufort West where outcrops start to only be found in the south-east, north of Oudshoorn and Willowmore, reaching up to areas south of Graaff-Reinet. Its northernmost exposures occur around the towns Fraserburg and Victoria West. The Tapinocephalus Assemblage Zone is the second biozone of the Beaufort Group.

<i>Cistecephalus</i> Assemblage Zone

The Cistecephalus Assemblage Zone is a tetrapod assemblage zone or biozone found in the Adelaide Subgroup of the Beaufort Group, a majorly fossiliferous and geologically important geological group of the Karoo Supergroup in South Africa. This biozone has outcrops located in the Teekloof Formation north-west of Beaufort West in the Western Cape, in the upper Middleton and lower Balfour Formations respectively from Colesberg of the Northern Cape to east of Graaff-Reinet in the Eastern Cape. The Cistecephalus Assemblage Zone is one of eight biozones found in the Beaufort Group, and is considered to be Late Permian in age.

<i>Euchambersia</i> Extinct genus of therapsid from Late Permian South Africa

Euchambersia is an extinct genus of therocephalian therapsids that lived during the Late Permian in what is now South Africa and China. The genus contains two species. The type species E. mirabilis was named by paleontologist Robert Broom in 1931 from a skull missing the lower jaw. A second skull, belonging to a probably immature individual, was later described. In 2022, a second species, E. liuyudongi, was named by Jun Liu and Fernando Abdala from a well-preserved skull. It is a member of the family Akidnognathidae, which historically has also been referred by as the synonymous Euchambersiidae.

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

Burnetiidae is an extinct family of biarmosuchian therapsids that lived in the Permian period whose fossils are found in South Africa and Russia. It contains Bondoceras, Bullacephalus, Burnetia, Mobaceras, Niuksenitia, Paraburnetia and Proburnetia.

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

Proburnetia is an extinct genus of biarmosuchian therapsids in the family Burnetiidae, from the Late Permian of Russia. It had bizarre bumps and protrusions on its skull.

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

Lemurosaurus is a genus of extinct biarmosuchian therapsids from the Late Permian of South Africa. The generic epithet Lemursaurus is a mix of Latin, lemures “ghosts, spirits”, and Greek, sauros, “lizard”. Lemurosaurus is easily identifiable by its prominent eye crests, and large eyes. The name Lemurosaurus pricei was coined by paleontologist Robert Broom in 1949, based on a single small crushed skull, measured at approximately 86 millimeters in length, found on the Dorsfontein farm in Graaff-Reinet. To date, only two skulls of the Lemurosaurus have been discovered, so body size is unknown. The second larger, more intact, skull was found in 1974 by a team from the National Museum, Bloemfontein.

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

Paraburnetia is an extinct genus of biarmosuchian therapsids from the Late Permian of South Africa. It is known for its species P. sneeubergensis and belongs to the family Burnetiidae. Paraburnetia lived just before the Permian–Triassic mass extinction event.

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

Lobalopex is an extinct genus of biarmosuchian therapsids. It was alive during the Late Permian and has only been found in the Teekloof Formation in South Africa. The only known species of the genus is Lobalopex mordax. Lobalopex is part of the clade of Burnetiamorpha, which have fossil specimens located in multiple areas of Africa and Russia.

<i>Bullacephalus</i> Extinct genus of animal

Bullacephalus is an extinct genus of biarmosuchian therapsids belonging to the family Burnetiidae. The type species B. jacksoni was named in 2003. It is known from a relatively complete skull and lower jaw, discovered in the Late Permian Tapinocephalus Assemblage Zone of the Beaufort Group of South Africa. This genus of therapsida lived during the Late Permian period, approximately 250 million years ago. The name Bullacephalus comes from the Latin words "bullatus," meaning "bossed" or "knobbed," and "cephalus," meaning "head." This name refers to the distinctive bony knob on the top of the therapsid's skull, which contributes to the history of this genus. This stem based taxon includes Ictidorhinus or Hippasaurs. Bullacephalus can even be characterized as having a, “skull moderately to greatly pachyostotic; swollen boss present above the postorbital bar formed by the postfrontal and postorbital; deep linear sculpturing of the snout; exclusion of the jugal from the lateral temporal fenestra”. These Therapsids have spongy bone skull roof, palatal process of premaxilla are long, diverticulum of naris adding them to the Burnetiamorph. Furthermore, the discovery of Bullacephalus has helped to refine the taxonomic classification of therapsids. Prior to its discovery, there was uncertainty regarding the relationship between different groups of therapsids, particularly the Burnetiamorpha and the Biarmosuchia. However, the distinctive features of Bullacephalus suggest that it is a member of the Burnetiamorpha, and provides a bridge between this group and the Biarmosuchia. The discovery of Bullacephalus has also highlighted the importance of continued exploration and excavation in areas that have yielded few therapsid fossils. The Beaufort Group of South Africa, where Bullacephalus was discovered, has been an important site for therapsid fossils, but much of the area remains unexplored. Further discoveries in this region and other areas around the world may provide new insights into the evolution and diversification of therapsids, as well as other groups of extinct animals. These discoveries will also help to refine our understanding of the history of life on Earth and the processes that have shaped the diversity of organisms that exist today.

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

Eriphostoma is an extinct genus of gorgonopsian therapsids known from the Middle Permian of Tapinocephalus Assemblage Zone, South Africa. It has one known species, Eriphostoma microdon, and was first named by Robert Broom in 1911. It is the oldest known gorgonopsian and among the smallest and most basal members of the clade.

<i>Eosimops</i> Extinct genus of dicynodonts

Eosimops is an extinct genus of pylaecephalid dicynodonts. They were small synapsids superficially resembling modern mammals. Eosimops is known from several skull specimens, as well as one complete skeleton. Eosimops lived during the Middle Permian of South Africa.

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

Ictidorhinus is an extinct genus of biarmosuchian therapsids. Fossils have been found from the Dicynodon Assemblage Zone of the Beaufort Group in the Karoo Basin, South Africa and are of Late Permian age. It had a short snout and proportionally large orbits. These characteristics may be representative of a juvenile animal, possibly of Lycaenodon. However, these two genera are not known to have existed at the same time, making it unlikely for Ictidorhinus material to be from a juvenile form of Lycaenodon.

Lycaenodon is an extinct genus of biarmosuchian therapsids from the Late Permian of South Africa. It is known from a single species, Lycaenodon longiceps, which was named by South African paleontologist Robert Broom in 1925. Both are small-bodied biarmosuchians. Two specimens are known, and both preserve only the front portions of the skull. These specimens come from the Cistecephalus Assemblage Zone of the Karoo Basin. Broom attributed the back portion of a third skull to Lycaenodon, but subsequent examiners considered it to belong to a gorgonopsian or dinocephalian and not a biarmosuchian. Most of the distinguishing features of Lycaenodon come from its palate. As a member of Biarmosuchia, the most basal group of therapsids, Lycaenodon shares many features with earlier and less mammal-like synapsids like Dimetrodon.

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

Pachydectes is an extinct genus of biarmosuchian therapsids from the Middle Permian of South Africa known from a single skull. The etymology of the name Pachydectes is derived from the Greek word pakhus, meaning "thick" or "thickened", and dektes, meaning "biter". In conjunction this name is representative of the unique pachyostotic bone present above the maxillary canine tooth found in the skull of the specimen. There is only one known species within the genus, Pachydectes elsi which is named in honor of the person who discovered the fossil.

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

Herpetoskylax is an extinct genus of biarmosuchians which existed in South Africa. The type species is Herpetoskylax hopsoni. It lived in the Late Permian Period.

Christian Alfred Sidor is an American vertebrate paleontologist. He is currently a Professor in the Department of Biology, University of Washington in Seattle, as well as Curator of Vertebrate Paleontology and Associate Director for Research and Collections at the Burke Museum of Natural History and Culture. His research focuses on Permian and Triassic tetrapod evolution, especially on therapsids.

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

Leucocephalus is a genus of biarmosuchian belonging to the family Burnetiidae dating to the Wuchiapingian. It was found in the Tropidostoma Assemblage Zone of the Main Karoo Basin of South Africa. It is a monotypic taxon which contains one only species, Leucocephalus wewersi. The genus name Leucocephalus is derived from Greek. Leucos, meaning white; kephalos, meaning skull, as the Leucocephalus skull discovered was unusually pale. The species epithet wewersi comes from the farm employee who found the skull, Klaus ‘Klaasie’ Wewers.

References

  1. 1 2 3 4 5 6 7 Rubidge, Bruce S.; Sidor, Christian A. (2002). "On the cranial morphology of the basal therapsids Burnetia and Proburnetia (Therapsida: Burnetiidae)" (PDF). Journal of Vertebrate Paleontology. 22 (2): 257–267. doi:10.1671/0272-4634(2002)022[0257:OTCMOT]2.0.CO;2. S2CID   86207308. Archived from the original (PDF) on 2006-09-16. Retrieved 2012-02-12.
  2. 1 2 3 4 5 6 7 Boonstra, Lieuwe D. (1934-07-01). "On an Aberrant Gorgonopsian, Burnetia Mirabilis Broom". South African Journal of Science. 31 (7): 462–470. ISSN   0038-2353.
  3. Rubidge, Bruce S.; Sidor, Christian A. (2002). "On the Cranial Morphology of the Basal Therapsids Burnetia and Proburnetia (Therapsida: Burnetiidae)". Journal of Vertebrate Paleontology. 22 (2): 257–267. doi:10.1671/0272-4634(2002)022[0257:OTCMOT]2.0.CO;2. ISSN   0272-4634. JSTOR   4524220. S2CID   86207308.
  4. 1 2 3 4 Sidor, Christian A.; Hopson, James A.; Keyser, André W. (2004). "A New Burnetiamorph Therapsid from the Teekloof Formation, Permian, of South Africa". Journal of Vertebrate Paleontology. 24 (4): 938–950. doi:10.1671/0272-4634(2004)024[0938:ANBTFT]2.0.CO;2. ISSN   0272-4634. JSTOR   4524788. S2CID   85752458.
  5. 1 2 "Lende chiweta, a new therapsid from Malawi, and its influence on burnetiamorph phylogeny and biogeography". ResearchGate. Retrieved 2020-03-07.
  6. 1 2 Rubidge, Bruce S.; Sidor, Christian A.; Modesto, Sean P. (2006). "A New Burnetiamorph (Therapsida: Biarmosuchia) from the Middle Permian of South Africa". Journal of Paleontology. 80 (4): 740–749. doi:10.1666/0022-3360(2006)80[740:ANBTBF]2.0.CO;2. ISSN   0022-3360. JSTOR   4095109. S2CID   130196490.
  7. 1 2 Sidor, Christian A. (2003). "The Naris and Palate of Lycaenodon longiceps (Therapsida: Biarmosuchia), with Comments on Their Early Evolution in the Therapsida". Journal of Paleontology. 77 (5): 977–984. ISSN   0022-3360. JSTOR   4094766.
  8. Sidor, Christian A.; Angielczyk, Kenneth D.; Weide, D. Marie; Smith, Roger M. H.; Nesbitt, Sterling J.; Tsuji, Linda A. (2010-05-18). "Tetrapod fauna of the lowermost Usili Formation (Songea Group, Ruhuhu Basin) of southern Tanzania, with a new burnetiid record". Journal of Vertebrate Paleontology. 30 (3): 696–703. doi:10.1080/02724631003758086. ISSN   0272-4634. S2CID   55397720.