Euryapsida

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A euryapsid skull. Skull euryapsida 1.svg
A euryapsid skull.

Euryapsida is a polyphyletic (unnatural, as the various members are not closely related) group of sauropsids that are distinguished by a single temporal fenestra, an opening behind the orbit, under which the post-orbital and squamosal bones articulate. They are different from Synapsida, which also have a single opening behind the orbit, by the placement of the fenestra. In synapsids, this opening is below the articulation of the post-orbital and squamosal bones. It is now commonly believed that euryapsids (particularly sauropterygians) are in fact diapsids (which have two fenestrae behind the orbit) that lost the lower temporal fenestra. Euryapsids are usually considered entirely extinct, although turtles might be part of the sauropterygian clade [1] while other authors disagree. [2] Euryapsida may also be a synonym of Sauropterygia sensu lato. [3]

The ichthyosaurian skull is sometimes described as having a metapsid (or parapsid) condition instead of a truly euryapsid one. In ichthyosaurs, the squamosal bone is never part of the fenestra's margin. [4] Parapsida was originally a taxon consisting of ichthyosaurs, squamates, protorosaurs, araeoscelidans and pleurosaurs. [3]

Historically, a variety of reptiles with upper fenestrae, either alone or with a lower emargination, have been considered euryapsid or parapsid, and to have had their patterns of fenestration originate separately from those of diapsids. This includes araeoscelidans, mesosaurs, squamates, pleurosaurids, [5] weigeltisaurids, protorosaurs, and trilophosaurs. [6] [7] With the exception of mesosaurs, which only have the lower temporal opening, all of these are universally agreed to be diapsids which either secondarily closed the lower opening (araeoscelids, trilophosaurs) or lost the lower bar (squamates, pleurosaurs, protorosaurs).

Euryapsida was proposed by Edwin H. Colbert as a substitute for the earlier term Synaptosauria, originally created by Edward D. Cope for a taxon including sauropterygians, turtles and rhynchocephalians. Baur removed the rhynchocephalians from Synaptosauria and Williston later resurrected the taxon, including only Sauropterygia (Nothosauria and Plesiosauria) and Placodontia in it. [3]

A parapsid skull. Skull parapsida 1.png
A parapsid skull.

The terms Enaliosauria and Halisauria have also been used for a taxon including ichthyosaurs and sauropterygians. [8] [9]

Some 21st century studies have found that ichthyosaurs, thalattosaurs and sauropterygians were close relatives, either as stem-archosaurs [2] [10] or as stem-saurians. [11] [12]

See also

Related Research Articles

<span class="mw-page-title-main">Anapsid</span> Subclass of reptiles

An anapsid is an amniote whose skull lacks one or more skull openings 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.

<span class="mw-page-title-main">Amniote</span> Clade of tetrapods including reptiles, birds and mammals

Amniotes are tetrapod vertebrate animals belonging to the clade Amniota, a large group that comprises the vast majority of living terrestrial and semiaquatic vertebrates. Amniotes evolved from amphibian ancestors during the Carboniferous period and further diverged into two groups, namely the sauropsids and synapsids. They are distinguished from the other living tetrapod clade — the non-amniote lissamphibians — by the development of three extraembryonic membranes, thicker and keratinized skin, and costal respiration.

<span class="mw-page-title-main">Lepidosauria</span> Superorder of reptiles

The Lepidosauria is a subclass or superorder of reptiles, containing the orders Squamata and Rhynchocephalia. Squamata includes lizards and snakes. Squamata contains over 9,000 species, making it by far the most species-rich and diverse order of non-avian reptiles in the present day. Rhynchocephalia was a formerly widespread and diverse group of reptiles in the Mesozoic Era. However, it is represented by only one living species: the tuatara, a superficially lizard-like reptile native to New Zealand.

<span class="mw-page-title-main">Diapsid</span> Clade of amniote tetrapods with two holes in each side of their skulls

Diapsids are a clade of sauropsids, distinguished from more primitive eureptiles by the presence of two holes, known as temporal fenestrae, in each side of their skulls. The group first appeared about three hundred million years ago during the late Carboniferous period. All diapsids other than the most primitive ones in the clade Araeoscelidia are sometimes placed into the clade Neodiapsida. The diapsids are extremely diverse, and include birds and all modern reptile groups, including turtles, which were historically thought to lie outside the group. 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.

The quadratojugal is a skull bone present in many vertebrates, including some living reptiles and amphibians.

<span class="mw-page-title-main">Mesosaur</span> Extinct family of reptiles

Mesosaurs were a group of small aquatic reptiles that lived during the early Permian period (Cisuralian), roughly 299 to 270 million years ago. Mesosaurs were the first known aquatic reptiles, having apparently returned to an aquatic lifestyle from more terrestrial ancestors. It is uncertain which and how many terrestrial traits these ancestors displayed; recent research cannot establish with confidence if the first amniotes were fully terrestrial, or only amphibious. Most authors consider mesosaurs to have been aquatic, although adult animals may have been amphibious, rather than completely aquatic, as indicated by their moderate skeletal adaptations to a semiaquatic lifestyle. Similarly, their affinities are uncertain; they may have been among the most basal sauropsids or among the most basal parareptiles.

<span class="mw-page-title-main">Sauropterygia</span> Group of Mesozoic aquatic reptiles

Sauropterygia is an extinct taxon of diverse, aquatic reptiles that developed from terrestrial ancestors soon after the end-Permian extinction and flourished during the Triassic before all except for the Plesiosauria became extinct at the end of that period. The plesiosaurs would continue to diversify until the end of the Mesozoic. Sauropterygians are united by a radical adaptation of their pectoral girdle, adapted to support powerful flipper strokes. Some later sauropterygians, such as the pliosaurs, developed a similar mechanism in their pelvis.

<span class="mw-page-title-main">Archosauromorpha</span> Infraclass of reptiles

Archosauromorpha is a clade of diapsid reptiles containing all reptiles more closely related to archosaurs rather than lepidosaurs. Archosauromorphs first appeared during the late Middle Permian or Late Permian, though they became much more common and diverse during the Triassic period.

<span class="mw-page-title-main">Trilophosauridae</span> Extinct family of reptiles

Trilophosaurs are lizard-like Triassic allokotosaur reptiles related to the archosaurs. The best known genus is Trilophosaurus, a herbivore up to 2.5 metres long. It had a short, unusually heavily built skull, equipped with massive, broad flattened cheek teeth with sharp shearing surfaces for cutting up tough plant material. Teeth are absent from the premaxilla and front of the lower jaw, which in life were probably equipped with a horny beak.

<span class="mw-page-title-main">Parareptilia</span> Subclass of reptiles

Parareptilia ("near-reptiles") is a subclass or clade of basal sauropsids/reptiles, typically considered the sister taxon to Eureptilia. Parareptiles first arose near the end of the Carboniferous period and achieved their highest diversity during the Permian period. Several ecological innovations were first accomplished by parareptiles among reptiles. These include the first reptiles to return to marine ecosystems (mesosaurs), the first bipedal reptiles, the first reptiles with advanced hearing systems, and the first large herbivorous reptiles. The only parareptiles to survive into the Triassic period were the procolophonoids, a group of small generalists, omnivores, and herbivores. The largest family of procolophonoids, the procolophonids, rediversified in the Triassic, but subsequently declined and became extinct by the end of the period.

<i>Cyamodus</i> Extinct genus of reptiles

Cyamodus is a genus of placodonts known from several species described from Middle-Late Triassic of Europe and China. The genus was described by Christian Erich Hermann von Meyer in 1863, based on specimens found in Germany. Like some other placodonts, Cyamodus has an armoured carapace composed of irregular hexagonal plates, with the mouth containing a small number of large, rounded teeth that were likely involved in crushing hard shelled organisms (durophagy).

<span class="mw-page-title-main">Thalattosauria</span> Extinct order of sea reptiles

Thalattosauria is an extinct order of prehistoric 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.

<span class="mw-page-title-main">Temporal fenestra</span> Opening in the skull behind the orbit in some animals

Temporal fenestrae are openings in the temporal region of the skull of some amniotes, behind the orbit. These openings have historically been used to track the evolution and affinities of reptiles. Temporal fenestrae are commonly seen in the fossilized skulls of dinosaurs and other sauropsids. The major reptile group Diapsida, for example, is defined by the presence of two temporal fenestrae on each side of the skull. The infratemporal fenestra, also called the lateral temporal fenestra or lower temporal fenestra, is the lower of the two and is exposed primarily in lateral (side) view.

<i>Acerosodontosaurus</i> Extinct genus of reptiles

Acerosodontosaurus is an extinct genus of neodiapsid reptiles that lived during the Upper Permian of Madagascar. The only species of Acerosodontosaurus, A. piveteaui, is known from a natural mold of a single partial skeleton including a crushed skull and part of the body and limbs. The fossil was discovered in deposits of the Lower Sakamena Formation. Based on skeletal characteristics, it has been suggested that Acerosodontosaurus individuals were at least partially aquatic.

<i>Helveticosaurus</i> Extinct genus of reptiles

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.

<span class="mw-page-title-main">Evolution of reptiles</span> Origin and diversification of reptiles through geologic time

Reptiles arose about 320 million years ago during the Carboniferous period. Reptiles, in the traditional sense of the term, are defined as animals that have scales or scutes, lay land-based hard-shelled eggs, and possess ectothermic metabolisms. So defined, the group is paraphyletic, excluding endothermic animals like birds that are descended from early traditionally-defined reptiles. A definition in accordance with phylogenetic nomenclature, which rejects paraphyletic groups, includes birds while excluding mammals and their synapsid ancestors. So defined, Reptilia is identical to Sauropsida.

<i>Hanosaurus</i> Extinct genus of reptiles

Hanosaurus is an extinct genus of marine reptiles that existed during the Triassic period in what is now China. The type species is Hanosaurus hupehensis. It was a small animal, with specimens measuring 79.4 cm (31.3 in) long in total body length, which likely fed on soft-bodied prey.

<i>Palatodonta</i> Extinct genus of reptiles

Palatodonta is an extinct genus of neodiapsid reptile known from the early Middle Triassic of the Netherlands. It was initially described in 2013 as a basal placodontiform closely related to a group of marine reptiles called placodonts, characterized by their crushing teeth and shell-like body armor. Under this interpretation, Palatodonta is transitional between placodonts and less specialized reptiles. Like placodonts, it has a row of large teeth on its palate, but while these teeth are thick and blunt in placodonts, Palatodonta has palatal teeth that are thin and pointed. A 2023 study instead classified it as a sauropterygomorph and the sister taxon to Eusaurosphargis. In other words, it is close to, but not within, Sauropterygia.

<span class="mw-page-title-main">Pantestudines</span> Clade of reptiles

Pantestudines or Pan-Testudines is the group of all reptiles more closely related to turtles than to any other living animal. It includes both modern turtles and all of their extinct relatives. Pantestudines with a complete shell are placed in the clade Testudinata.

<i>Taytalura</i> Extinct genus of reptiles

Taytalura is an extinct genus of lepidosauromorph reptile from the Late Triassic of Argentina. It contains a single species, Taytalura alcoberi, which is based on a well-preserved skull from the fossiliferous Ischigualasto Formation. As a lepidosauromorph, Taytalura is a distant relative of modern lepidosaurs such as sphenodontians and squamates. Taytalura did not belong to any group of modern lepidosaurs, since it bears unique features, such as unfused bones in the skull roof and teeth which all sit loosely in a deep groove without sockets. Regardless, Micro-CT scanning reveals features of the skull previously only seen in rhynchocephalians. This suggests that the ancestral condition of the skull in lepidosaurs was more similar to sphenodonts than to squamates.

References

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