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Temporal range: Early Triassic, 251–247  Ma
Thrinaxodon liorhinus skeleton.jpg
Fossil of T. liorhinus in National Museum of Natural History
The American Museum journal (c1900-(1918)) (18161901551).jpg
Diagram of skull in lateral view
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Animalia
Phylum: Chordata
Clade: Synapsida
Clade: Therapsida
Clade: Cynodontia
Clade: Epicynodontia
Family: Thrinaxodontidae
Watson & Romer, 1956
Genus: Thrinaxodon
Seeley, 1894
Type species
Thrinaxodon liorhinus
Seeley, 1894

Thrinaxodon is an extinct genus of cynodonts, including the species T. liorhinus which lived in what are now South Africa and Antarctica during the Early Triassic. Thrinaxodon lived just after the Permian–Triassic mass extinction event, its survival during the extinction may have been due to its burrowing habits. [1]


Similar to other therapsids, Thrinaxodon adopted a semi-sprawling posture, an intermediary form between the sprawling position of basal tetrapods (still observed modern Crocodilia) and the more upright posture present in current mammals. [2] Thrinaxodon is prevalent in the fossil record in part because it was one of the few carnivores of its time, and was of a larger size than similar cynodont carnivores.[ citation needed ]


Restoration Thrinaxodon BW.jpg

Thrinaxodon was a small synapsid roughly the size of a fox [1] and possibly covered in hair. The dentition suggests that it was a carnivore, focusing its diet mostly on insects, small herbivores and invertebrates. Their unique secondary palate successfully separated the nasal passages from the rest of the mouth, allowing the Thrinaxodon to continue mastication without interrupting to breathe, an adaptation important for digestion.[ citation needed ]


The nasals of Thrinaxodon are pitted with a large number of foramina. The nasals narrow anteriorly and expand anteriorly and articulate directly with the frontals, pre-frontals and lacrimals; however, there is no interaction with the jugals or the orbitals. The maxilla of Thrinaxodon is also heavily pitted with foramina. [3] The arrangement of foramina on the snout of Thrinaxodon resembles lizards such as Tupinambis more than mammals, which bear a single large infraorbital foramen. [3] [4] As such, Thrinaxodon would have had non-muscular lips like those of lizards, not mobile, muscular ones like those of mammals. [3] Without the infraorbital foramen and its associated facial flexibility, it is unlikely that Thrinaxodon would have had whiskers. [4] [5]

On the skull roof of Thrinaxodon, the fronto-nasal suture represents an arrow shape instead of the general transverse process seen in more primitive skull morphologies. The prefrontals, which are slightly anterior and ventral to the frontals exhibit a very small size and come in contact with the post-orbitals, frontals, nasals and lacrimals. More posteriorly on the skull, the parietals lack a sagittal crest. The cranial roof is the narrowest just posterior to the parietal foramen, which is very nearly circular in shape. The temporal crests remain quite discrete throughout the length of the skull. The temporal fenestra have been found with ossified fasciae, giving evidence of some type of a temporal muscle attachment. [3]

The upper jaw contains a secondary palate which separates the nasal passages from the rest of the mouth, which would have given Thrinaxodon the ability to breathe uninterrupted, even if food had been kept in its mouth. This adaptation would have allowed the Thrinaxodon to mash its food to a greater extent, decreasing the amount of time necessary for digestion. The maxillae and palatines meet medially in the upper jaw developing a midline suture. The maxillopalatine suture also includes a posterior palatine foramen. The large palatal roof component of the vomer in Thrinaxodon is just dorsal to the choana, or interior nasal passages. The pterygoid bones extend in the upper jaw and enclose small interpterygoid vacuities that are present on each side of the cultriform processes of the parasphenoids. The parasphenoid and basisphenoid are fused, except for the most anterior/dorsal end of the fused bones, in which there is a slight separation in the trabecular attachment of the basisphenoid. [3]

The skull of specimen AMNH 5630 in the American Museum of Natural History, from South Africa Thrinaxodon liorhinus AMNH 5630.jpg
The skull of specimen AMNH 5630 in the American Museum of Natural History, from South Africa

The otic region is defined by the regions surrounding the temporal fenestrae. Most notable is evidence of a deep recess that is just anterior to the fenestra ovalis, containing evidence of smooth muscle interactions with the skull. Such smooth muscle interactions have been interpreted to be indicative of the tympanum and give the implications that this recess, in conjunction with the fenestra ovalis, outline the origin of the ear in Thrinaxodon. This is a new synapomorphy as this physiology had arisen in Thrinaxodon and had been conserved through late Cynodontia. The stapes contained a heavy cartilage plug, which was fit into the sides of the fenestra ovalis; however, only one half of the articular end of the stapes was able to cover the fenestra ovalis. The remainder of this pit opens to an "un-ossified" region which comes somewhat close to the cochlear recess, giving one the assumption that inner ear articulation occurred directly within this region. [3]

The skull of Thrinaxodon is an important transitional fossil which supports the simplification of synapsid skulls over time. The most notable jump in bone number reduction had occurred between Thrinaxodon and Probainognathus, a change so dramatic that it is most likely that the fossil record for this particular transition is incomplete. Thrinaxodon contains fewer bones in the skull than that of its pelycosaurian ancestors. [6]


Data on the dentition of Thrinaxodon liorhinus was compiled by use of a micro CT scanner on a large sample of Thrinaxodon skulls, ranging between 30 and 96 mm (1.2 and 3.8 in) in length. These dentition patterns are similar to that of Morganucodon , allowing one to make the assumption that these dentition patterns arose within Thrinaxodontidae and extended into the records of early Mammalia. Adult T. liorhinus assumes the dental pattern of the four incisors, one canine and six postcanines on each side of the upper jaw. This pattern is reflected in the lower jaw by a dental formula of three incisors, one canine and seven or eight postcanines on each side of the lower jaw. With this formula, one can make a small note that in general, adult Thrinaxodon contained anywhere between 44 and 46 total teeth. [7]

Upper incisors in T. liorhinus assume a backwards directed cusp, and they go from being curved and pointed at their most distal point, and become broader and rounder as they reach their proximal insertion point into the premaxilla. The fourth upper incisor greatly resembles the form of that of a small canine; however, it is positioned too far anteriorly to be a functional canine. Lower incisors possess a very broad base, which is progressively reduced, heading distally towards the tip of the tooth. The lingual face of the lower incisors are most often concave while the labial face is often convex, and these lower incisors are oriented anteriorly, except in some cases for the third lower incisor, which can assume a more dorsoventral orientation. The incisors are, for the most part, single functional teeth encompassing a broad, cone-like morphology. The canines of T. liorhinus possess small dorsoventrally directed facets on their surfaces, by our[ who? ] understanding, these facets are related to occlusion. Each canine possesses a replacement canine located within the jaw, posterior to the existing canine, neither of the replacement or functional canine teeth possess any serrated margins only the small facets. It is important to note that the lower canine is directed almost vertically (dorsoventrally) while the upper canine is directed slightly anteriorly. [7]

Fossil in CosmoCaixa Barcelona Thrinaxodon liorhinus.jpg
Fossil in CosmoCaixa Barcelona

The upper and lower postcanines in T. liorhinus share some common features but also vary quite a fair amount in comparison to one another. The first postcanine (just posterior to the canine) is most often smaller than the other postcanines and is most often bicuspid. Including the first postcanine, if any of the other postcanines are bicuspid, then it is safe to assume that the posterior accessary cusp is present and that that tooth will not have any cingular or labial cusps. If, however, the tooth is tricuspid, then there is a chance of cingular cusps developing, if this occurs then the anterior cusp will be the first to appear and will be the most pronounced cusp. In the upper postcanines, there should be no occurrence of any teeth possessing more than 3 cusps, and there is no occurrence of any labial cusps on the upper postcanines. The majority of upper postcanines in the juvenile Thrinaxodon are bicuspid, while only one of these upper teeth are tricuspid. The upper postcanines of an intermediate (between juvenile and adult) Thrinaxodon are all tricuspid with no labial or cingular cusps. The adult upper postcanines retain the intermediate physiologies and possess only tricuspid teeth; however, it is possible for cingular cusps to develop in these adult teeth. The ultimate (posterior-most) upper canine is often the smallest of all canines in the entire jaw system. Little data is known of the juvenile and intermediate forms of the lower postcanines in Thrinaxodon, but the adult lower postcanines all possess multiple (any value more than three) cusps as well as the only appearance of labial cusps. Some older specimens have been found that possess no multiple-cups lower canines, possibly a response to old age or teeth replacement. [7]

Thrinaxodon shows one of the first occurrences of replacement teeth in cynodonts. This was discerned by the presence of replacement pits, which are situated lingual to the functional tooth in the incisors and postcanines. While a replacement canine does exist, more often than not it is not erupted and the original functional canine remains. [7]


Vertebrae and ribs of specimen AMNH 9516 in the American Museum of Natural History, from Antarctica Thrinaxodon liorhinus AMNH 9516 cast.jpg
Vertebrae and ribs of specimen AMNH 9516 in the American Museum of Natural History, from Antarctica

The bone tissue of Thrinaxodon consists of fibro-lamellar bone, to a varying degree across all the separate limbs, most of which develops into parallel-fibred bone tissue towards the periphery. Each of the bones contains a large abundance of globular osteocyte lacunae which radiate a multitude of branched canaliculi. Ontogenetically early bones, of which are mostly fibro-lamellar tissue, possessed a large amount of vascular canals. These canals are oriented longitudinally within primary osteons that contain radial anastomoses. Regions consisting mostly of parallel-fibred bone tissue contain few simple vascular canals, in comparison to the nearby fibro-lamellar tissues. Parallel-fibred peripheral bone tissue are indicative that bone growth began to slow, and they bring about the assumption that this change in growth was due to the age of the specimen in question. Combine this with the greater organization of osteocyte lacunae in the periphery of adult T. liorhinus, and we approach the assumption that this creature grew very quickly in order to reach adulthood at an accelerated rate. Before Thrinaxodon, ontogenical patterns such as this had not been seen, establishing the idea that reaching peak size rapidly was an adaptively advantageous trait that had arisen with Thrinaxodon. [8]

Within the femur of Thrinaxodon, there is no major region of the bone that is made of parallel-fibred tissues; however, there is a small ring of parallel-fibred bone within the mid-cortex. The remainder of the femur is made of fibro-lamellar tissue; however, the globular osteocyte lacunae become much more organized and the primary osteons assume less vasculature than many other bones as you begin to approach the subperiosteal surface. The femur contains very few bony trabeculae. The humerus differs from the femur in many regards, one of which being that there is a more extensive network of bony trabeculae in the humerus near the meduallary cavity of the bone. The globular osteocyte lacunae become more flattened as you get closer and closer to the midshaft of the humerus. While the vasculature is present, the humerus contains no secondary osteons. The radii and ulnae of Thrinaxodon represent roughly the same histological patterns. In contrast to the humerii and femora, the parallel-fibred region is far more distinct in the distal bones of the forelimb. The medullary cavities are surrounded by multiple layers of very poorly vascularized endosteal lamellar tissue, along with very large cavities near the medullary cavity of the metaphyses. [8]

Discovery and naming

Two South African specimens preserved together Iziko Thrinaxodon fossil.JPG
Two South African specimens preserved together

Thrinaxodon was originally discovered in the Lystrosaurus Assemblage Zone of the Beaufort Group of South Africa. The genoholotype, BMNH R 511, was in 1887 described by Richard Owen as the plesiotype of Galesaurus planiceps. [9] In 1894 it was by Harry Govier Seeley made a separate genus with as type species Thrinaxodon liorhinus. Its generic name was taken from the Ancient Greek for "trident tooth", thrinax and odon. The specific name is Latinised Greek for "smooth-nosed".

Thrinaxodon was initially believed to be isolated to that region. Other fossils in South Africa were recovered from the Normandien and Katberg Formations. [10] It had not been until 1977 that additional fossils of Thrinaxodon had been discovered in the Fremouw Formation of Antarctica. Upon its discovery there, numerous experiments were done to confirm whether or not they had found a new species of Thrinaxodontidae, or if they had found another area which T. liorhinus called home. The first experiment was to evaluate the average number of pre-sacral vertebrae in the Antarctic vs African Thrinaxodon. The data actually showed a slight difference between the two, in that the African T. liorhinus contained 26 presacrals, while the Antarctic Thrinaxodon had 27 pre-sacrals. In comparison to other cynodonts, 27 pre-sacrals appeared to be the norm throughout this sub-section of the fossil record. The next step was to evaluate the size of the skull in the two different discovery groups, and in this study they found no difference between the two, the first indication that they may in fact be of the same species. The ribs were the final physiology to be cross-examined, and while they portrayed slight differences in the expanded ribs, against one another, the most important synapomorphy remained consistent between the two, and that was that the intercostal plates overlapped with one another. These evaluations led to the conclusion that they had not found a new species of Thrinaxodontidae, but yet they had found that Thrinaxodon occupied two different geographical regions, which today are separated by an immense expanse of ocean. This discovery was one of many to support the idea of a connected land mass, and that during the early Triassic, Africa and Antarctica must have been linked in some way, shape or form. [11]


Reconstructed jaw adductor musculature Jaw adductor musculature of Thrinaxodon.jpg
Reconstructed jaw adductor musculature

Thrinaxodon belongs to the clade Epicynodontia, a subdivision of the greater clade Cynodontia. Cynodontia eventually led to the evolution of Morganucodon and all other mammalia. Cynodontia belongs to the clade Therapsida, which was the first major clade along the line of the Synapsida. Synapsida represents one of two major splitting points, under the clade Amniota, which also split into Sauropsida, the larger clade containing today's reptiles, birds and Crocodilia. Thrinaxodon represents a fossil transitional in morphology on the road to humans and other extant mammals.[ citation needed ]















There appear to be nine cranial features that successfully separate Thrinaxodon into four ontogenetic stages. The paper denotes that in general, the Thrinaxodon skull increased in size isometrically, except for four regions, one of which being the optic region. Much of the data assumes that the length of the sagittal crest increased at a greater rate in relation to the rest of the skull. The posterior sagittal crest to appear in an earlier ontogenetic stage than the more anterior crest had, and in conjunction with the dorsal deposition of bone, a unified sagittal crest had developed rather than having a single suture span the entire length of the skull. [12]

The bone histology of Thrinaxodon indicates that it most likely had very rapid bone growth during juvenile development, and much slower development throughout adulthood, giving rise to the idea that Thrinaxodon reached peak size very early in its life. [8]


The posture of Thrinaxodon is an interesting subject, because it represents a transition between the sprawling behavior of the more lizard-like pelycosaurs and the more upright behavior found in modern, and many extinct, Mammalia. In cynodonts such as Thrinaxodon, the distal femoral condyle articulates with the acetabulum in a way that permits the hindlimb to present itself at a 45-degree angle to the rest of the system. This is a large difference in comparison to the distal femoral condyle of pelycosaurs, which permits the femur to be parallel with the ground, forcing them to assume a sprawling-like posture. [2] More interesting is that there is an adaptation that has only been observed within Thrinaxodontidae, which allows them to assume upright posture, similar to that of early Mammalia, within their burrows. [1] These changes in posture are supported by the physiological changes in the torso of Thrinaxodon. Such changes as the first appearance of a segmented rib compartment, in which Thrinaxodon expresses both thoracic and lumbar vertebrae. The thoracic segment of the vertebrae contain ribs with large intercostal plates that most likely assisted with either protection or supporting the main frame of the back. This newly developed arrangement allowed for the appropriate space for a diaphragm, however, without proper soft tissue records, the presence of a diaphragm is purely speculative. [13]


CT image of specimen in burrow Thrinaxodon liorhinus BP 1 7199.jpg
CT image of specimen in burrow

Thrinaxodon has been identified as a burrowing cynodont by numerous discoveries in preserved burrow hollows. There is evidence that the burrows are in fact built by the Thrinaxodon to live in them, and they do not simply inhabit leftover burrows by other creatures. Due to the evolution of a segmented vertebral column into thoracic, lumbar and sacral vertebrae, Thrinaxodon was able to achieve flexibilities that permitted it to comfortably rest within smaller burrows, which may have led to habits such as aestivation or torpor. This evolution of a segmented rib cage suggests that this may have been the first instance of a diaphragm in the synapsid fossil record; however, without the proper soft tissue impressions this is nothing more than an assumption. [13] [1]

3D reconstruction of a Thrinaxodon liorhinus skeleton found in the same burrow with a Broomistega amphibian (synchrotron imaging) [14]

The earliest discovery of a burrowing Thrinaxodon places the specimen found around 251 million years ago, a time frame surrounding the Permian–Triassic extinction event. Much of these fossils had been found in the flood plains of South Africa, in the Karoo Basin. This behavior had been seen at a relatively low occurrence in the pre-Cenozoic, dominated by therapsids, early-Triassic cynodonts and some early Mammalia. Thrinaxodon was in fact the first burrowing cynodont that has been found, showing similar behavioral patterns to that of Trirachodon. The first burrowing vertebrate on record was the dicynodont synapsid Diictodon , and it is possible that these burrowing patterns had passed on to the future cynodonts due to the adaptive advantage of burrowing during the extinction. The burrow of Thrinaxodon consists of two laterally sloping halves, a pattern that has only been observed in burrowing non-mammalian Cynodontia. The changes in vertebral/rib anatomy that arose in Thrinaxodon permit the animals to a greater range of flexibility, and the ability to place their snout underneath their hindlimbs, an adaptive response to small living quarters, in order to preserve warmth and/or for aestivation purposes. [1]

A Thrinaxodon burrow contained an injured temnospondyl, Broomistega . The burrow was scanned using a synchrotron, a tool used to observe the contents of the burrows in this experiment, and not damage the intact specimens. The synchrotron revealed an injured rhinesuchid, Broomistegaputterilli, showing signs of broken or damaged limbs and two skull perforations, most likely inflicted by the canines of another carnivore. The distance between the perforations was measured in relation to the distance between the canines of the Thrinaxodon in question, and no such relation was found. Therefore, we may assume that the temnospondyl found refuge in the burrow after a traumatic experience and the T. liorhinus allowed it to stay in its burrow until they both ultimately met their respective deaths. Interspecific shelter sharing is a rare anomaly within the fossil record; this T. liorhinus shows one of the first occurrences of this type of behavior in the fossil record, but it currently is unknown if the temnospondyl inhabited the burrow before or after the death of the nesting Thrinaxodon. [15]

See also

Related Research Articles

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Probainognathus meaning “progressive jaw” is an extinct genus of cynodonts that lived around 235 to 221.5 million years ago, during the Late Triassic in what is now Argentina. Together with the genus Bonacynodon from Brazil, Probainognathus forms the family Probainognathidae. Probainognathus was a relatively small, carnivorous or insectivorous cynodont. Like all cynodonts, it was a relative of mammals, and it possessed several mammal-like features. Like some other cynodonts, Probainognathus had a double jaw joint, which not only included the quadrate and articular bones like in more basal synapsids, but also the squamosal and surangular bones. A joint between the dentary and squamosal bones, as seen in modern mammals, was however absent in Probainognathus.

<i>Galesaurus</i> Extinct genus of cynodonts from the Triassic of South Africa

Galesaurus is an extinct genus of carnivorous cynodont therapsid that lived between the Induan and the Olenekian stages of the Early Triassic in what is now South Africa. It was incorrectly classified as a dinosaur by Sir Richard Owen in 1859.

Tritylodontidae is an extinct family of small to medium-sized, highly specialized mammal-like cynodonts, bearing several mammalian traits like erect limbs, endothermy and details of the skeleton. They were the last-known family of the non-mammaliaform synapsids, persisting into the Early Cretaceous.

<i>Bauria</i> Genus of therapsids from the Earlt Triassic of South Africa

Bauria is an extinct genus of the suborder Therocephalia that existed during the Early and MiddleTriassic period, around 246-251 million years ago. It belonged to the family Bauriidae. Bauria was probably a carnivore or insectivore. It lived in South Africa, specifically in the Burgersdorp Formation in South Africa.

<i>Prozostrodon</i> Extinct genus of cynodonts

Prozostrodon is an extinct genus of probainognathian cynodonts that was closely related to the ancestors of mammals. The remains were found in Brazil and are dated to the Carnian age of the Late Triassic. The holotype has an estimated skull length of 6.7 centimetres (2.6 in), indicating that the whole animal may have been the size of a cat. The teeth were typical of advanced cynodonts, and the animal was probably a carnivore hunting reptiles and other small prey.

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

Moschorhinus is an extinct genus of therocephalian in the family Akidnognathidae with only one species: M. kitchingi. It was a carnivorous synapsid which has been found in the Late Permian to Early Triassic of the South African Karoo Supergroup. It was a large carnivore, reaching 1.5 m (4.9 ft) in total body length with the largest skull comparable to that of a lion in size. It had a broad, blunt snout which bore long, straight canines. It appears to have replaced the gorgonopsids ecologically, and hunted much like a big cat. While most abundant in the Late Permian, it survived a little after the Permian Extinction, though these Triassic individuals had stunted growth.

<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>Brasilodon</i> Extinct genus of mammaliamorphs

Brasilodon is an extinct genus of small, mammal-like cynodonts that lived in what is now Brazil during the Norian age of the Late Triassic epoch, about 225.42 million years ago. While no complete skeletons have been found, the length of Brasilodon has been estimated at around 12 centimetres (4.7 in). Its dentition shows that it was most likely an insectivore. The genus is monotypic, containing only the species B. quadrangularis. Brasilodon belongs to the family Brasilodontidae, whose members were some of the closest relatives of mammals, the only cynodonts alive today. Two other brasilodontid genera, Brasilitherium and Minicynodon, are now considered to be junior synonyms of Brasilodon.

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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> Genus of therapsid from the Late Permian of South Africa

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>Progalesaurus</i> Extinct genus of cynodonts

Progalesaurus is an extinct genus of galesaurid cynodont from the early Triassic. Progalesaurus is known from a single fossil of the species Progalesaurus lootsbergensis, found in the Lystrosaurus Assemblage Zone of the Balfour Formation. Close relatives of Progalesaurus, other galesaurids, include Galesaurus and Cynosaurus. Galesaurids appeared just before the Permian-Triassic extinction event, and disappeared from the fossil record in the Middle-Triassic.

<i>Platycraniellus</i> Extinct genus of cynodonts from the early Triassic of South Africa

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>Andescynodon</i> Extinct genus of cynodonts

Andescynodon is a genus of traversodontid cynodonts from the Middle Triassic of Argentina. Fossils are known from the Cerro de las Cabras and Cacheutá Formations. Andescynodon is one of the most basal traversodontids. Another traversodontid called Rusconiodon has also been identified from the Cerro de las Cabras Formation but is now considered a junior synonym of Andescynodon.

Boreogomphodon is an extinct genus of traversodontid cynodonts from the Late Triassic of the eastern United States. Fossils have been found from the Turkey Branch Formation in Virginia.

<i>Karenites</i> Genus of therapsids from the Late Permian of Russia

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<i>Cricodon</i> Extinct genus of cynodonts

Cricodon is an extinct genus of trirachodontid cynodonts that lived during the Early Triassic and Middle Triassic periods of Africa. A. W. Crompton named Cricodon based on the ring-like arrangement of the cuspules on the crown of a typical postcanine tooth. The epithet of the type species, C. metabolus, indicates the change in structure of certain postcanines resulting from replacement.

<i>Abdalodon</i> Extinct genus of cynodonts

Abdalodon is an extinct genus of late Permian cynodonts, known by its only species A. diastematicus.Abdalodon together with the genus Charassognathus, form the clade Charassognathidae. This clade represents the earliest known cynodonts, and is the first known radiation of Permian cynodonts.

<i>Bonacynodon</i> Extinct genus of cynodonts

Bonacynodon is an extinct genus of cynodonts that lived in what is now southern Brazil during the Triassic period. The genus is monotypic, containing only the type species Bonacynodon schultzi. B. schultzi is known from two specimens, consisting of two partial skulls and some badly preserved parts of the postcranium. Both specimens were recovered from the Pinheiros-Chiniquá Sequence, part of the Santa Maria Supersequence of the Paraná Basin. This sequence preserves a faunal association known as the Dinodontosaurus Assemblage Zone, which contains numerous other species of cynodonts, dicynodonts and reptiles. Bonacynodon was a small, likely insectivorous cynodont, whose length has been estimated at around 30 centimetres (12 in). It can be distinguished from other cynodonts by its large, serrated (saw-like) canine teeth. Together with the genus Probainognathus of Argentina, it made up the family Probainognathidae, one of the earliest-diverging lineages of the clade Probainognathia. It was a fairly close relative of mammals, the only group of cynodonts alive today.

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.


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Further reading