Karenites

Last updated

Karenites
Temporal range: Late Permian
Karenites ornamentatus.jpg
Life restoration of Karenites ornamentatus
Scientific classification Red Pencil Icon.png
Kingdom: Animalia
Phylum: Chordata
Clade: Therapsida
Suborder: Therocephalia
Family: Ictidosuchidae
Genus: Karenites
Tatarinov, 1995
Type species
Karenites ornamentatus
Tatarinov, 1995

Karenites is an extinct genus of therocephalian therapsids from the Late Permian of Russia. The only species is Karenites ornamentatus, named in 1995. Several fossil specimens are known from the town of Kotelnich in Kirov Oblast. [1]

Contents

Description

Karenites is known from a partial holotype skeleton, two partial skulls, and isolated jaw bones. Although incomplete, the skulls preserve small and delicate structures like nasal turbinates on the inside of the skull and the stapes bone of the ear. The skull of Karenites is about 10 centimetres (3.9 in) long, with the snout much longer than the temporal region of the skull behind the eye sockets. Viewed from above, the skull is triangular. The snout is broad, and the skull widens toward the occiput or posterior margin. Two large holes behind the eye socket called temporal fenestrae occupy most of the posterior skull. Between these fenestra is a narrow sagittal crest. In front of this crest, the skull roof bones are weakly pitted with small bumps and ridges for blood vessels. Some specimens include parts of the sclerotic ring, a ring of bone embedded in the eye. [1]

On each side of the upper jaw are five incisors, two or three precanines, one canine, and eleven or twelve postcanines. The incisors and precanines are long, thin, and slightly curved, separated from each other by a small gap. The canine is much longer, projecting slightly forward from the tooth socket and curving backward along its length. The postcanine teeth are shorter and broader than the incisors and precanines. Toward the back of the skull the tips of the teeth flatten. The lower jaw is thin and curves upward to the arch of the cheek, except for a large coronoid process that extends to the articular-quadrate jaw joint at the back of the skull. The lower jaw has three small incisors angled slightly forward, a large canine tooth projecting upward, and thirteen small, blunt postcanine teeth. The farthest postcanine teeth have small secondary cusps behind their tips. These multicusped teeth may have been adaptations for crushing food, although they are not as well developed as the teeth of other therocephalians like Ericiolacerta . [1]

In 1999, thoracic plates were reported to be present in the holotype of Karenites. [2] Thoracic plates are plates of bone on the underside of the rib cage that are typically found in reptiles, and unusual for mammal relatives like therocephalians. This bone was later reinterpreted as an interclavicle, part of the pectoral girdle common to all early therapsids. [1]

Paleobiology

The presence of a sclerotic ring in Karenites may be an indication that it was aquatic. Pits on the skull have been interpreted as evidence for well-developed whiskers, which may have been used in hunting aquatic prey. Some therocephalians like Perplexisaurus have also been interpreted as aquatic predators, and share many similarities with Karenites. While these aquatic forms had strong sutures between cranial bones, which may have stabilized the skull when consuming large aquatic prey like fishes, Karenites had weaker, slightly movable skull joints associated with feeding on smaller terrestrial prey like insects. Its multicuspid teeth also suggest it fed on insects. Karenites has long limb bones that indicate a fully terrestrial rather than aquatic lifestyle. [1]

Ridges on the inside of the skull of Karenites form a series of sinuses. These sinuses may have been associated with improvements in the sense of smell of therocephalians, but they are not thought to be olfactory structures. [1]

Bony projections on the underside of the lower jaw of Karenites may have supported tissues that transmitted sound to the stapes bone in the ear. Early therapsids like Karenites lack the well-developed auditory system of mammals, which had evolved from a restructuring of bones in the back of the skull and the lower jaw, and probably had a poor sense of hearing. As an early stage in the development of the mammalian auditory system, Karenites may have been able to hear some sounds by placing its jaw on the ground to detect vibrations. [3]

Related Research Articles

<i>Thrinaxodon</i> genus of mammals (fossil)

Thrinaxodon is an extinct genus of cynodonts, most commonly regarded by its species T. liorhinus which lived in what are now South Africa and Antarctica. Thrinaxodon has been dated between the Permian–Triassic boundary and the mid-Triassic. Its survival of the extinction may have been due to its burrowing habits.

Gorgonopsia suborder of synapsids (fossil)

Gorgonopsia is an extinct clade of non-mammalian synapsids from the Permian period. Gorgonopsians were quadrupedal predators with prominent canine teeth, and the largest species were the apex predators of their ecosystems. Like other non-mammalian synapsids, gorgonopsians were once described as "mammal-like reptiles", due to their mix of mammalian and reptilian traits. However, this description is no longer considered accurate as they are not reptiles. Rather, as therapsids, they are closely related to mammals. Gorgonopsian fossils have been found in Russia and Africa.

Therocephalia suborder of mammals (fossil)

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.

<i>Euchambersia</i> genus of mammals (fossil)

Euchambersia is a genus of therocephalian therapsid that lived during the Late Permian, approximately 255 million years ago, in what is now South Africa. The genus contains a single species, Euchambersia mirabilis, named by paleontologist Robert Broom in 1931 from a skull missing the lower jaws; a second skull, belonging to an immature individual, was later described. It is a member of the family Akidnognathidae, which historically has also been referred by as the synonymous Euchambersiidae.

<i>Moschorhinus</i> genus of mammals (fossil)

Moschorhinus is an extinct genus of therocephalian in the family Akidnognathidae, with only one species: M. kitchingi. It was a carnivorous, lion-sized synapsis which has been found in the Late Permian to Early Triassic of the South African Karoo Supergroup. 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> Genus of mammals (fossil)

Theriognathus is an extinct genus of therocephalian therapsid belonging to the family Whaitsiidae, from South Africa 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>Regisaurus</i> genus of mammals (fossil)

Regisaurus is an extinct genus of small carnivorous therocephalian. It is known from a single described species, the type species Regisaurus jacobi, from the Early Triassic Lystrosaurus Assemblage Zone of South Africa, although at least one undescribed species is also known.

<i>Glanosuchus</i> species of mammal (fossil)

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 mammals (fossil)

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.

Chlynovia is an extinct genus of therocephalian therapsids from the Late Permian of Russia. The type species is C. serridentatus, named in 2000. Chlynovia was originally classified within Scaloposauria, a group of therocephalians characterized by their small size and lightly built skulls. Scaloposaurians are no longer recognized as a true grouping, but instead represent the juvenile forms of many types of therocephalians. Chlynovia was placed in the family Perplexisauridae along with Perplexisaurus, but both therocephalians are now placed in the family Ictidosuchidae.

Bauriidae family of mammals (fossil)

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>Purlovia</i> genus of mammals (fossil)

Purlovia is an extinct genus of herbivorous therocephalian therapsids from the Late Permian of Russia. Together with the closely related South African genus Nanictidops, it is a member of the family Nanictidopidae. Fossils have been found from the Tonshayevsky District of Nizhny Novgorod Oblast. The type species of Purlovia, P. maxima, was named in 2011.

Nanictidopidae family of mammals (fossil)

Nanictidopidae is an extinct family of therocephalian therapsids from the Late Permian. Two genera are currently included in the family, Nanictidops from South Africa and Purlovia from Russia. Nanictidopids have short skulls and were probably herbivorous.

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.

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.

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.

Phthinosaurus is an extinct genus of therapsids from the Middle Permian of Russia. The type species Phthinosaurus borrisiaki was named by Soviet paleontologist Ivan Yefremov in 1940 on the basis of an isolated lower jaw. Because this jaw provides few distinguishing characteristics, the evolutionary relationships of Phthinosaurus are poorly known. Yefremov named the family Phthinosuchidae in 1954 to include Phthinosaurus and the newly named Phthinosuchus, which was described on the basis of a crushed partial skull. American paleontologist Everett C. Olson placed both of these therapsids in the larger infraorder Phthinosuchia in 1961. In 1974 Leonid Tatarinov named the family Phthinosauridae to include Phthinosaurus alone, retaining Phthinosuchus within Phthinosuchidae.

Rubidgeinae subfamily of mammals (fossil)

Rubidgeinae is an extinct subfamily of gorgonopsid therapsids known only from Africa. They were among the largest gorgonopsians, and their fossils are common in the Cistecephalus and Daptocephalus assemblage zones of the Karoo Basin. They lived during the Late Permian, and became extinct at the end of the Permian.

<i>Abdalodon</i> genus of therapsids

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>Nochnitsa</i> genus of mammals (fossil)

Nochnitsa is a genus of gorgonopsian therapsid from the Kotelnich red beds of Permian Russia. It contains one species, Nochnitsa geminidens. It the most basal known gorgonopsian and among the smallest members of the clade known to date.

References

  1. 1 2 3 4 5 6 Ivakhnenko, M.F. (2011). "Permian and Triassic therocephals (Eutherapsida) of Eastern Europe". Paleontological Journal. 45 (9): 981–1144. doi:10.1134/S0031030111090012.
  2. Tatarinov, L.P. (2004). "The postcranial skeleton of the Late Permian scaloposaurian Karenites ornamentatus (Reptilia, Theriodontia) from the Kirov Region". Paleontological Journal. 38 (5): 548–555.
  3. Tatarinov, L.P. (1995). "A new ictidosuchid Karenites ornamentatus (Theriodontia) from the Upper Permian of the Kotel'nich locality in the Kirov Region". Russian Journal of Herpetology. 2 (1): 18–33.