Acrodonty (from Greek akros 'highest' [1] + odont- 'tooth') is an anatomical placement of the teeth at the summit of the alveolar ridge of the jaw, without sockets, [2] characteristic of bony fish. Functionally, acrodont tooth implantation may be related to greater bite force. [3] However, this result is not supported when size and phylogeny is taken into account. [4]
Squamata: Within squamate reptiles, acrodont tooth implantation is best known in Acrodonta and some species of amphisbaenians, though some snakes are also referred to as being acrodont. Acrodonta is unique in that the name of the clade is based upon this trait. Most other squamate reptiles have pleurodont dentition, though some snakes are occasionally described as having acrodont dentition. [5] [6]
Rhynchocephalia: Acrodont tooth implantation is common within Rhynchocephalia, including Sphenodon . [7]
Amphibia: Acrodont tooth implantation also present in some frogs and the temnospondyl Microposaurus . [8] [9] [10]
Rhynchocephalia is an order of lizard-like reptiles that includes only one living species, the tuatara of New Zealand. Despite its current lack of diversity, during the Mesozoic rhynchocephalians were a speciose group with high morphological and ecological diversity. The oldest record of the group is dated to the Middle Triassic around 238 to 240 million years ago, and they had achieved global distribution by the Early Jurassic. Most rhynchocephalians belong to the group Sphenodontia ('wedge-teeth'). Their closest living relatives are lizards and snakes in the order Squamata, with the two orders being grouped together in the superorder Lepidosauria.
Choristodera is an extinct order of semiaquatic diapsid reptiles that ranged from the Middle Jurassic, or possibly Triassic, to the Miocene. Choristoderes are morphologically diverse, with the best known members being the crocodile-like neochoristoderes such as Champsosaurus. Other choristoderans had lizard-like or long necked morphologies. Choristoderes appear to have been confined to the Northern Hemisphere, having been found in North America, Asia, and Europe, and possibly also North Africa. Choristoderes are generally thought to be derived neodiapsids that are close relatives or members of Sauria.
Temnospondyli or temnospondyls is a diverse ancient order of small to giant tetrapods—often considered primitive amphibians—that flourished worldwide during the Carboniferous, Permian and Triassic periods, with fossils being found on every continent. A few species continued into the Jurassic and Early Cretaceous periods, but all had gone extinct by the Late Cretaceous. During about 210 million years of evolutionary history, they adapted to a wide range of habitats, including freshwater, terrestrial, and even coastal marine environments. Their life history is well understood, with fossils known from the larval stage, metamorphosis and maturity. Most temnospondyls were semiaquatic, although some were almost fully terrestrial, returning to the water only to breed. These temnospondyls were some of the first vertebrates fully adapted to life on land. Although temnospondyls are amphibians, many had characteristics such as scales and large armour-like bony plates (osteoderms) that generally distinguish them from the modern soft-bodied lissamphibians.
Homoeosaurus is an extinct genus of rhynchocephalian reptile, known from the Late Jurassic-earliest Cretaceous of Europe, with specimens being reported from France, England and Germany. Several species have been described within the genus, based on varying proportions of the limb bones to the body length based on the presacral vertebrae. Specimen C.M.6438 of H. maximiliani from Germany has a total length of around 17 centimetres (6.7 in), with a skull length of about 1.7 centimetres (0.67 in). In comparison to other rhynchocephalians, the limbs are proportionally long. Recent studies have classified Homoeosaurus as a member of Neosphenodontia, with some studies including it as part of the clade Leptorhynchia, also including sapheosaurs, pleurosaurs, Kallimodon and Vadasaurus. Despite being found in aquatic deposits, it is suggested to have been terrestrial. It is thought to have been a carnivore/insectivore. One specimen was found as stomach contents of the fish Belonostomus.
The interdental plate refers to the bone-filled mesial-distal region between the teeth. The word "interdental" is a combination of "inter" + "dental" which originated in approximately 1870. In paleobiology, the presence or absence of the interdental plate can determine the place of an animal in the evolutionary scale, and paleontologists use the interdental plate when trying to classify a new specimen. Thecodont reptiles and theropod dinosaur fossils have an interdental plate, whereas acrodont reptiles such as Sphenodontia do not. Its presence in Archaeopteryx, an extinct avialan, resulted in the proposal of the dinosaur-bird connection.
Thalattosauria is an extinct order of marine reptiles that lived in the Middle to Late Triassic. 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.
Leptopleuron is an extinct genus of procolophonid that lived in the dry lands during the late Triassic in Elgin of northern Scotland and was the first to be included in the clade of Procolophonidae. First described by English paleontologist and biologist Sir Richard Owen, Leptopleuron is derived from two Greek bases, leptos for "slender" and pleuron for "rib," describing it as having slender ribs. The fossil is also known by a second name, Telerpeton, which is derived from the Greek bases tele for "far off" and herpeton for "reptile." In Scotland, Leptopleuron was found specifically in the Lossiemouth Sandstone Formation. The yellow sandstone it was located in was poorly lithified with wind coming from the southwest. The environment is also described to consist of barchan dunes due to the winds, ranging up to 20 m tall that spread during dry phases into flood plains. Procolophonoids such as Leptopleuron were considered an essential addition to the terrestrial ecosystem during the Triassic.
Colobomycter is an extinct genus of acleistorhinid parareptile known from the Early Permian of Oklahoma.
Lydekkerinidae is a family of stereospondyl temnospondyls that lived in the Early Triassic period. During this time period, lydekkerinids were widely distributed, with putative remains reported from Russia, Greenland, India, South Africa, Madagascar, Australia, and Antarctica. In contrast to most other stereospondyls, lydekkerinids were relatively small-bodied. The type genus is Lydekkerina, the namesake of the family and the best-known lydekkerinid.
Trematosaurinae is a subfamily of temnospondyl amphibians within the family Trematosauridae. Like all trematosaurids, they were marine piscivores, resembling crocodiles in their general build. Unlike the long, almost gharial-like snouts of the Lonchorhynchinae, the Trematosaurinae had more "normal" crocodile-like skulls.
Theretairus is a Late Jurassic genus of sphenodont reptile from the Morrison Formation of western North America, present in stratigraphic zones 5 and 6.
Brachyopomorpha is a clade of stereospondyl temnospondyls within the infraorder Trematosauria. It was constructed in 2000 to include Bothriceps australis and the superfamily Brachyopoidea. It is phylogenetically defined as a stem-based taxon including Pelorocephalus and all taxa closer to it than to Rhytidosteus. In contrast, Brachyopoidea is defined as a node-based taxon including Brachyops and Pelorocephalus and all descendants of their most recent common ancestor. Because Bothriceps is not thought to be a descendant of that recent common ancestor and would be more basal than it, the genus is placed just outside Brachyopoidea and is considered to be a sister taxon to the clade.
Pasawioops is an extinct genus of early Permian dissorophoid temnospondyl within the clade Amphibamiformes.
Cargninia is an extinct genus of basal lepidosauromorph from the Late Triassic of Brazil. The type and only known species is Cargninia enigmatica. It is known from the holotype UFRGS PV 1027 T, a partial left dentary found in what is now Faxinal do Soturno, Rio Grande do Sul, southern Brazil, in the geopark Paleorrota. This locality is from the middle section of the Norian-age Caturrita Formation. Cargninia was named by José Fernando Bonaparte, César Leandro Schultz, Marina Bento Soares and Agustín G. Martinelli in 2010. The generic name honors Daniel Cargnin, a Brazilian priest and fossil collector, and the specific name means “enigmatic”, in reference to its uncertain phylogenetic placement.
Thecodont dentition is a morphological arrangement in which the base of the tooth is completely enclosed in a deep socket of bone, as seen in crocodilians, dinosaurs and mammals, and opposed to acrodont and pleurodont dentition seen in squamate reptiles. Notably, this appears to be the ancestral tooth condition in Amniota. This morphology was once used as a basis for the now-defunct taxonomic group Thecodontia.
Bharatagama is an extinct genus of lepidosaur from the Early Jurassic of India. It has been suggested to be one of the oldest known lizards and the oldest known iguanian. The type and only species is Bharatagama rebbanensis, named in 2002. Over one hundred fossils of Bharatagama have been found in the Kota Formation, which outcrops in the Pranhita–Godavari Basin and dates back to about 190 million years ago (Ma). Despite its abundance, Bharatagama is known only from isolated jaw bones mixed together in microvertebrate assemblages with equally fragmentary remains of fish, sphenodontians, dinosaurs, crocodylomorphs, and mammals. These fossils represent all stages of development, from hatchlings to adults. The total length of the skull in adult specimens is estimated to have been about 15 millimetres (0.59 in). Later analysis suggested that the taxon might be a member of Rhynchocephalia.
Sphenovipera jimmysjoyi is an extinct species of sphenodontian dated from the Middle Jurassic. If was discovered in the lower part of the La Boca Formation located in Tamaulipas, Mexico. Only the lower jaw of this organism has been discovered and studied. It is possibly the only species of rhynchocephalian yet discovered to show evidence of venom delivery.
Acrodonta are a subclade of iguanian squamates consisting almost entirely of Old World taxa. Extant representation include the families Chamaeleonidae (chameleons) and Agamidae, with at least over 500 species described. A fossil genus, Gueragama, was found in Brazil, making it the only known American representative of the group.
Dolichosauridae is a family of Cretaceous aquatic lizards. They are widely considered to be the earliest and most primitive members of Mosasauria, though some researchers have recovered them as more closely related to snakes.
Palacrodon is an extinct genus of Triassic reptile with a widespread distribution. It was initially described from teeth collected in Early Triassic deposits in South Africa, and later reported from the Early Triassic of Antarctica and the Late Triassic of Arizona. Although previously considered an early rhynchocephalian, it is currently considered to be a non-saurian neodiapsid.