| Stauromatodon Temporal range: Middle Triassic, Ladinian | |
|---|---|
Scientific classification  | |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Reptilia |
| Clade: | Diapsida |
| Genus: | † Stauromatodon Sobral, Sues & Schoch, 2021 |
| Type species | |
| †Stauromatodon mohli Sobral, Sues & Schoch, 2021 | |
Stauromatodon is an extinct genus of diapsid reptile, possibly related to Saurosphargidae, from the Middle Triassic Erfurt Formation of Germany. It contains a single species, Stauromatodon mohli. [1]
An anapsid is an amniote whose skull lacks one or more skull openings (fenestra) near the temples. Traditionally, the Anapsida are the most primitive subclass of amniotes, the ancestral stock from which Synapsida and Diapsida evolved, making anapsids paraphyletic. It is however doubtful that all anapsids lack temporal fenestra as a primitive trait, and that all the groups traditionally seen as anapsids truly lacked fenestra.
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 study concluded that Tetraceratops is not a true therapsid, but should be considered a member of the more ancient Sphenacodontia, from which the therapsids evolved.
Lepidosauromorpha is a group of reptiles comprising all diapsids closer to lizards than to archosaurs. The only living sub-group is the Lepidosauria, which contains two subdivisions, Squamata, which contains lizards and snakes, and Rhynchocephalia, the only extant species of which is the tuatara.
Rhynchosaurs are a group of extinct herbivorous Triassic archosauromorph reptiles, belonging to the order Rhynchosauria. Members of the group are distinguished by their triangular skulls and elongated, beak like premaxillary bones. Rhynchosaurs first appeared in the Middle Triassic or possibly the Early Triassic, before becoming abundant and globally distributed during the Carnian stage of the Late Triassic.
Avicephala is an extinct, potentially polyphyletic grouping of diapsid reptiles that lived during the Late Permian and Triassic periods characterised by superficially bird-like skulls and arboreal lifestyles. As a clade, Avicephala is defined as including the gliding weigeltisaurids and the arboreal drepanosaurs to the exclusion of other major diapsid groups. This relationship is not recovered in the majority of phylogenetic analyses of early diapsids and so Avicephala is typically regarded as an unnatural grouping. However, the clade was recovered again in 2021 in a redescription of Weigeltisaurus, raising the possibility that the clade may be valid after all.
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.
Drepanosaurs are a group of reptiles that lived between the Carnian and Rhaetian stages of the late Triassic Period, approximately between 230 and 210 million years ago. The various species of drepanosaurid were characterized by specialized grasping limbs and often prehensile tails, adaptions for arboreal (tree-dwelling) and fossorial (digging) lifestyles, with some having also been suggested to be aquatic. Fossils of drepanosaurs have been found in Arizona, New Mexico, New Jersey, Utah, England, and northern Italy. The name is taken from the family's namesake genus Drepanosaurus, which means "sickle lizard", a reference to their strongly curved claws.
Thalattosauria is an extinct order of prehistoric marine reptiles that lived in the middle to late Triassic period. Thalattosaurs were diverse in size and shape, and are divided into two superfamilies: Askeptosauroidea and Thalattosauroidea. Askeptosauroids were endemic to the Tethys Ocean, their fossils have been found in Europe and China, and they were likely semiaquatic fish eaters with straight snouts and decent terrestrial abilities. Thalattosauroids were more specialized for aquatic life and most had unusual downturned snouts and crushing dentition. Thalattosauroids lived along the coasts of both Panthalassa and the Tethys Ocean, and were most diverse in China and western North America. The largest species of thalattosaurs grew to over 4 meters (13 feet) in length, including a long, flattened tail utilized in underwater propulsion. Although thalattosaurs bore a superficial resemblance to lizards, their exact relationships are unresolved. They are widely accepted as diapsids, but experts have variously placed them on the reptile family tree among Lepidosauromorpha, Archosauromorpha, ichthyosaurs, and/or other marine reptiles.
Malerisaurus is an extinct genus of archosauromorph known from Andhra Pradesh of India and Texas of the USA.
Tangasauridae is a family of diapsids. Specimens have been found that are of Late Permian to Early Triassic in age from the Sakamena Group of western Madagascar. They lived alongside other taxa present from the Sakamena Group, including temnospondyls, rhynchosaurs, and gomphodont eucynodonts. Fossils have been found of numerous specimens of common members of this family such as Hovasaurus and Thadeosaurus in different stages of ontogenic development. Recent material from the Middle Sakamena Formation of the Morondava Basin of Madagascar that dates back to the early Triassic period suggests that the Tangasauridae were relatively unaffected by the Permian-Triassic extinction event.
Kuehneosauridae is an extinct family of small, lizard-like gliding diapsids known from the Triassic period of Europe and North America. They are distinguished from other diapsids by their 'wings' formed by elongated ribs. These allowed the animal to glide and parachute similar to living gliding lizards. They were most likely insectivorous, judging from their pin-like teeth. They are often, but not always, placed in the group Lepidosauromorpha, though other studies have recovered them in other positions within Sauria, including Archosauromorpha. The oldest and most primitive known member is Pamelina from the Early Triassic of Poland, which already has vertebrae with characteristics consistent with gliding or parachuting. Icarosaurus is known from a single specimen from the Carnian-aged Lockatong Formation of New Jersey. The Late Triassic kuehneosaurids from England, Kuehneosaurus and Kuehneosuchus, are very similar and can be distinguished from one another primarily on the length of their "wing" ribs, relatively short and massive in Kuehneosaurus but longer and more gracile in Kuehneosuchus. Kuehneosaurus was likely only capable of parachuting, while Kuehneosuchus could probably glide. Rhabdopelix may have been a kuehneosaurid; however, the fossils were lost, and the characteristics described are not entirely consistent with the other family members.
Helveticosaurus is an extinct genus of diapsid marine reptile known from the Middle Triassic of southern Switzerland. It contains a single species, Helveticosaurus zollingeri, known from the nearly complete holotype T 4352 collected at Cava Tre Fontane of Monte San Giorgio, an area well known for its rich record of marine life during the Middle Triassic.
Kenyasaurus is an extinct genus of basal neodiapsid, possibly tangasaurid, known from the Early Triassic period of Coast Province, southeastern Kenya. It contains a single species, Kenyasaurus mariakaniensis.
Younginidae is an extinct family of diapsid reptiles from the Late Permian and Early Triassic. In a phylogenetic context, younginids are near the base of the clade Neodiapsida. Younginidae includes the species Youngina capensis from the Late Permian of South Africa and Thadeosaurus colcanapi from the Late Permian and Early Triassic of Madagascar. Heleosuchus griesbachi from the Late Permian of South Africa may also be a member of the family.
Almadasuchus is an extinct genus of crocodylomorph known from the early Middle Jurassic Puesto Almada Member of the Cañadón Asfalto Formation of Patagonia, Argentina. It contains a single species, Almadasuchus figarii. It is known from the holotype MPEF-PV 3838, a well-preserved posterior region of the skull as well as other skull and postcranial remains.
Pappochelys is an extinct genus of diapsid reptile closely related to turtles. The genus contains only one species, Pappochelys rosinae, from the Middle Triassic of Germany, which was named by paleontologists Rainer Schoch and Hans-Dieter Sues in 2015. The discovery of Pappochelys provides strong support for the placement of turtles within Diapsida, a hypothesis that has long been suggested by molecular data, but never previously by the fossil record. It is morphologically intermediate between the definite stem-turtle Odontochelys from the Late Triassic of China and Eunotosaurus, a reptile from the Middle Permian of South Africa.
Eusaurosphargis is an extinct genus of a diapsid reptile, known from the Middle Triassic Besano Formation of northern Italy and Prosanto Formation of south-eastern Switzerland. It contains a single species, Eusaurosphargis dalsassoi.
Helveticosauridae is an extinct family of basal marine reptiles known from the Middle Triassic of southern Switzerland and northern Italy.
Ozimek is a genus of sharovipterygid protorosaur, a type of gliding Triassic archosauromorph reptile from Poland closely related to the Kyrgyzstani Sharovipteryx. It contains one species, O. volans, named in 2016 by Dzik and Sulej.
Dinocephalosauridae is an extinct family of marine and terrestrial archosauromorph reptiles that lived throughout the Triassic period. Like tanystropheids, they are characterized by their long necks, lengthened by either addition of cervical vertebrae or elongation of the individual bones.
