This article has multiple issues. Please help improve it or discuss these issues on the talk page . (Learn how and when to remove these template messages) (Learn how and when to remove this template message)
|
Eotitanosuchidae | |
---|---|
Life restoration of the eotitanosuchid Eotitanosuchus olsoni | |
Scientific classification | |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Therapsida |
Suborder: | † Biarmosuchia |
Infraorder: | † Eotitanosuchia Boonstra, 1963 |
Family: | † Eotitanosuchidae Tchudinov, 1960 |
Type species | |
† Eotitanosuchus olsoni Tchudinov, 1960 | |
Genera | |
|
Eotitanosuchidae is an extinct family of biarmosuchian therapsids. The Eotitanosuchidae were large predatory therapsids of the Wordian epoch. It was once considered to belong to a separate infraorder of therapsids called Eotitanosuchia.
The Eotitanosuchians seem to be more advanced than the Biarmosuchia in that the temporal opening behind the eye socket—although small—is still somewhat larger than the biarmosuchians; it is expanded in the upper rear (posterodorsal) margin, allowing the area of attachment of the adductor (jaw closing) muscles to be visible from the dorsal (top) view looking down. The eotitanosuchian bite was stronger and more efficient than the biarmosuchian bite. For this reason, some paleontologists see the eotitanosuchids as transitional between the biarmosuchians and higher therapsids. It is at least as likely that features of a larger temporal opening—and hence increased muscle mass and biting power—evolved simultaneously among a number of early therapsid groups, due to the obvious advantages this adaptation conferred. One must be wary in applying cladistic methodology to characteristics that are likely to evolve simultaneously among many competing lineages. In other respects the eotitanosuchians are quite primitive; they were the least modified in their jaw apparatus from their sphenacodont ancestry.
Synapsids are a group of animals that includes mammals and every animal more closely related to mammals than to the other members of the amniote clade, such as reptiles and birds. They are easily separated from other amniotes by having a temporal fenestra, an opening low in the skull roof behind each eye, leaving a bony arch beneath each; this accounts for their name. Primitive synapsids are usually called pelycosaurs or pelycosaur-grade synapsids. This informal term consists of all synapsids that are not therapsids, a monophyletic, more advanced, mammal-like group. The non-mammalian synapsids were described as mammal-like reptiles in classical systematics, but this misleading terminology is no longer in use as synapsids as a whole are no longer considered reptiles. They are now more correctly referred to as stem mammals or proto-mammals.
Therapsida is a major group of eupelycosaurian synapsids that includes mammals and their ancestors. 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. The earliest fossil attributed to Therapsida used to be Tetraceratops insignis from the Lower Permian. However in 2020, a new study has found that Tetraceratops is not actually a true Therapsid, but should be considered to be a member of the more ancient Sphenacodontia from which the therapsids evolved.
Dinocephalia is a clade of large-bodied early therapsids that flourished for a brief time in the Middle Permian between 270 and 260 million years ago (Ma), but became extinct, leaving no descendants. Dinocephalians included herbivorous, carnivorous, and omnivorous forms. Many species had thickened skulls with many knobs and bony projections. Dinocephalians were the first non-mammalian therapsids to be scientifically described and their fossils are known from Russia, China, Brazil, South Africa, Zimbabwe, and Tanzania.
Gorgonopsia is an extinct clade of sabre-toothed therapsids from the Middle to Upper Permian roughly 265 to 252 million years ago. They are characterised by a long and narrow skull, as well as elongated upper and sometimes lower canine teeth and incisors which were likely used as slashing and stabbing weapons. Postcanine teeth are generally reduced or absent. For hunting large prey, they possibly used a bite-and-retreat tactic, ambushing and taking a debilitating bite out of the target, and following it at a safe distance before its injuries exhausted it, whereupon the gorgonopsian would grapple the animal and deliver a killing bite. They would have had an incredible gape, possibly in excess of 90°, without having to unhinge the jaw.
Biarmosuchus is an extinct genus of biarmosuchian therapsids that lived around 267 mya during the Middle Permian period. Biarmosuchus was discovered in the Perm region of Russia. The first specimen was found in channel sandstone that was deposited by flood waters originating from the young Ural Mountains.
Eotitanosuchus is an extinct genus of biarmosuchian therapsids whose fossils were found in the town of Ochyor in Perm Krai, Russia. It lived about 267 million years ago. The only species is Eotitanosuchus olsoni.
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.
Anteosaurs are a group of large, primitive carnivorous dinocephalian therapsids with large canines and incisors and short limbs, that are known from the Middle Permian of South Africa, Russia, China, and Brazil. Some grew very large, with skulls 50–80 centimetres (20–31 in) long, and were the largest predators of their time. They died out at the end of the Middle Permian, possibly as a result of the extinction of the herbivorous Tapinocephalia on which they may have fed.
Therocephalia is an extinct suborder of eutheriodont therapsids from the Permian and Triassic. 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. This relationship takes evidence in a variety of skeletal features. The phylogeny of therocephalians has been disputed, as the monophyly of the group and the relationships of its members are unclear.
The theriodonts or Theriodontia are a major group of therapsids. They can be defined in traditional, Linnaean terms, in which case they are a suborder of synapsids that lived from the Middle Permian to the Middle Cretaceous, or in cladistic terms, in which case they include not only the traditional theriodonts but also their descendants the mammals as well.
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 Graff-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 in Bloemfontein.
Kamagorgon is an extinct genus of therapsids from the Middle Permian of Russia. The type and only species is Kamagorgon ulanovi. It is only known from an incomplete skull. The snout is short and the canine teeth are very large. Kamagorgon was named in 1998 and originally classified in the biarmosuchian family Eotitanosuchidae along with the poorly known therapsid Eotitanosuchus. More recently, Kamagorgon has considered as a primitive gorgonopsian rather than a biarmosuchian due to the length of the front jawbone and rear side of the skull. These features are commonly shared by the brithopodid and biarmosuchid lineages.
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.
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.
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.
Biseridens is an extinct genus of anomodont therapsid, and one of the most basal anomodont genera known. Originally known from a partial skull misidentified as an 'eotitanosuchian' in 1997, another well-preserved skull was found in the Xidagou Formation, an outcropping in the Qilian Mountains of Gansu, China, in 2009 that clarified its relationships to anomodonts, such as the dicynodonts.
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.
Ustia is an extinct genus of biarmosuchian therapsids from the Middle Permian of Russia. It is known from a single species, Ustia atra, which was described in 2003 from an isolated lower jaw. Ustia was classified in the family Ictidorhinidae, which also includes the genus Ictidorhinus from South Africa. Both are relatively small biarmosuchians. Several other Russian therapsids known only from lower jaw bones have been placed in Ictidorhinidae, and the family is likely a paraphyletic assemblage representing a small body type than a true clade.
Leucocephalus is a genus of biarmosuchian belonging to the family Burnetiidae dating to the Wuchiapingian. It was found in the Tropidostoma Assemblage Zone (Tropidostoma) 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. Wewersi comes from the farm employee who found the skull, Klaus ‘Klaasie’ Wewers.