The splenial is a small bone in the lower jaw of reptiles, amphibians and birds, usually located on the lingual side (closest to the tongue) between the angular and surangular. [1] [2]
The splenial is a small bone in the lower jaw of reptiles, amphibians and birds, usually located on the lingual side (closest to the tongue) between the angular and surangular. [1] [2]
Reptiles, as most commonly defined, are the animals in the class Reptilia, a paraphyletic grouping comprising all sauropsid amniotes except Aves (birds). Living reptiles comprise turtles, crocodilians, squamates and rhynchocephalians (tuatara). In the traditional Linnaean classification system, birds are considered a separate class to reptiles. However, crocodilians are more closely related to birds than they are to other living reptiles, and so modern cladistic classification systems include birds within Reptilia, redefining the term as a clade. Other cladistic definitions abandon the term reptile altogether in favor of the clade Sauropsida, which refers to all animals more closely related to modern reptiles than to mammals. The study of the traditional reptile orders, historically combined with that of modern amphibians, is called herpetology. The study of all reptiles combines herpetology and ornithology.
Synapsids are one of the two major groups of animals that evolved from basal amniotes, the other being the sauropsids, the group that includes reptiles, dinosaurs, and birds. The group includes mammals and every animal more closely related to mammals than to sauropsids. Unlike other amniotes, synapsids have a temporal fenestra, an opening low in the skull roof behind each eye, leaving a bony arch beneath each; this accounts for their name. The distinctive temporal fenestra developed about 318 million years ago during the Late Carboniferous period, when synapsids and sauropsids diverged.
Diapsids are a group of amniote tetrapods that developed two holes in each side of their skulls about 300 million years ago during the late Carboniferous period. The diapsids are extremely diverse, and include all crocodilians, lizards, snakes, tuatara, turtles, and birds. Although some diapsids have lost either one hole (lizards), or both holes, or have a heavily restructured skull, they are still classified as diapsids based on their ancestry. At least 17,084 species of diapsid animals are extant: 9,159 birds, and 7,925 snakes, lizards, tuatara, turtles, and crocodiles.
Archosauromorpha is a clade of diapsid reptiles containing all reptiles more closely related to archosaurs rather than lepidosaurs. Archosauromorphs first appeared during the middle Permian, though they became much more common and diverse during the Triassic period.
Leopold Joseph Franz Johann Fitzinger was an Austrian zoologist.
Nothosaurs were Triassic marine sauropterygian reptiles that may have lived like seals of today, catching food in water but coming ashore on rocks and beaches. They averaged about 3 metres (10 ft) in length, with a long body and tail. The feet were paddle-like, and are known to have been webbed in life, to help power the animal when swimming. The neck was quite long, and the head was elongated and flattened, and relatively small in relation to the body. The margins of the long jaws were equipped with numerous sharp outward-pointing teeth, indicating a diet of fish and squid.
Toxicofera is a proposed clade of scaled reptiles (squamates) that includes the Serpentes (snakes), Anguimorpha and Iguania. Toxicofera contains about 4,600 species, of extant Squamata. It encompasses all venomous reptile species, as well as numerous related non-venomous species. There is little morphological evidence to support this grouping, however it has been recovered by all molecular analyses as of 2012.
Petrolacosaurus is an extinct genus of diapsid reptile from the late Carboniferous period. It was a small, 40-centimetre (16 in) long reptile, and the earliest known reptile with two temporal fenestrae. This means that it was at the base of Diapsida, the largest and most successful radiation of reptiles that would eventually include all modern reptile groups, as well as dinosaurs and other famous extinct reptiles such as plesiosaurs, ichthyosaurs, and pterosaurs. However, Petrolacosaurus itself was part of Araeoscelida, a short-lived early branch of the diapsid family tree which went extinct in the mid-Permian.
The squamosal is a skull bone found in most reptiles, amphibians, and birds. In fishes, it is also called the pterotic bone.
Labidosaurus is an extinct genus of reptile from the Permian period of North America. Fossils have been discovered in Texas.
Hovasaurus is an extinct genus of diapsid reptile belonging to the order Eosuchia. It lived in what is now Madagascar during the Late Permian and Early Triassic, being a survivor of the Permian–Triassic extinction event and the paleontologically youngest member of the Tangasauridae. Fossils have been found in the Permian Lower and Triassic Middle Sakamena Formations of the Sakamena Group, where it is amongst the commonest fossils. Its morphology suggests an aquatic ecology.
Procolophon is a genus of lizard-like procolophonid parareptiles that first appeared in the Early Triassic (Induan) of South Africa, Brazil, and Antarctica. It persisted through the Permian–Triassic extinction event, but went extinct in the beginning of the Early Middle Triassic. The type species is P. trigoniceps.
Shokawa is an extinct genus of choristoderan diapsid reptile, known from the Lower Cretaceous of Japan. It is only known from one species, Shokawa ikoi. The only known remains are a postcranial specimen lacking the skull, discovered at the KO2 locality in sediments belonging to the Okurodani Formation near the village of Shokawa in Gifu Prefecture. Shokawa possessed a long neck with at least 16 cervical vertebrae, and closely resembles and is closely related to the smaller choristoderan, Hyphalosaurus. The generic name refers to the village near where it was found, while the specific name honors the collector of the first specimen, one Mr. Ikoi Shibata.
Anarosaurus is an extinct genus of pachypleurosaurs that lived in the Middle Triassic period (Anisian) and has been found in the Jena Formation and the Karlstadt Formation of Germany and the Winterswijk Quarry of The Netherlands. Two species are known: A. pumilio and A. heterodontus. The holotype of A. pumilio was originally housed at the Institut und Museum fur Geologie und Palaontologie, Georg-August-Universitat, Gottingen, but can no longer be located today because it was lost or destroyed during World War II.
Palatodonta is an extinct genus of basal placodontiform marine reptile known from the early Middle Triassic of the Netherlands. It is closely related to a group of marine reptiles called placodonts, characterized by their crushing teeth and shell-like body armor. Palatodonta is transitional between placodonts and earlier reptiles; like placodonts, it has teeth on its palate, but while these teeth are thick and blunt in placodonts, Palatodonta has palatal teeth that are thin and pointed.
Opisthodontosaurus is an extinct genus of captorhinid reptile from the Early Permian of Oklahoma. The type species Opisthodontosaurus carrolli was named in 2015 on the basis of several articulated skeletons from the Dolese Brothers Limestone Quarry near Richards Spur. Before the description of these skeletons, the jaws and teeth of Opisthodontosaurus carrolli were thought to belong to a species of lepospondyl amphibian called Euryodus primus. Although captorhinid reptiles and lepospondyl amphibians are distantly related, the two species show a remarkable degree of evolutionary convergence in their dental anatomy. Both were likely durophagous, eating hard-shelled invertebrates.
Vitalia is an extinct genus of reptile from the Early Triassic of European Russia known from the type species V. grata. It is known from the holotype dentary PIN 4173/126 as well as two additional dentaries PIN 1043/627 and 1043/628, all housed at the Paleontological Institute, Russian Academy of Sciences. The type dentary was originally included in the hypodigm of Coelodontognathus donensis named by the notable Russian vertebrate paleontologist Vitaliy Georgiyevich Ochev in 1967. Ivakhnenko (1973) separated the specimen and gave it its own genus and species name in light of the new material, which he named in honor of Ochev. The dentaries of Vitalia were collected at the Donskaya Luka Locality near the village of Sirotinskaya in Ilovlinsky District, Volgograd Oblast, from the Lipovskaya Formation of the Gamskii Horizon. Like Coelodontognathus, Vitalia was originally described as a procolophonid parareptile in 1973, but Arkhangelskii & Sennikov (2008) reclassified the taxon as a possible trilophosaurid archosauromorph. Vitalia is thought to be similar to the possible trilophosaurids Coelodontognathus and Doniceps, both of which are known exclusively from the same locality. Coelodontognathus and Vitalia are similar to procolophonids in that they have wide teeth but differs from them in that they have tooth roots set deep into the jaws.
Boreopricea is an extinct genus of archosauromorph reptile from the Early Triassic of arctic Russia. It is known from a fairly complete skeleton discovered in a borehole on Kolguyev Island, though damage to the specimen and loss of certain bones has complicated study of the genus. Boreopricea shared many similarities with various other archosauromorphs, making its classification controversial. Various studies have considered it a close relative of Prolacerta, tanystropheids, both, or neither. Boreopricea is unique among early archosauromorphs due to possessing contact between the jugal and squamosal bones at the rear half of the skull.
Zarcasaurus tanyderus is a species of araeoscelid reptile found in the Cutler Formation of New Mexico. The only elements of the skeleton known from this animal is a partial jaw bone, vertebrae, and broken limb bones.
Bothremys is an extinct genus of bothremydid pleurodiran turtle that was discovered near Gloucester, New Jersey. The genus consists of type species B. cooki, B. arabicus, B. kellyi, and B. maghrebiana.
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