Rhytidostea | |
---|---|
Life restoration of Lyddekerina huxleyi , a lydekkerinid and basal rhytidostean | |
Scientific classification | |
Kingdom: | Animalia |
Phylum: | Chordata |
Order: | † Temnospondyli |
Suborder: | † Stereospondyli |
Clade: | † Rhytidostea Shoch and Milner, 2000 |
Superfamilies and families | |
Rhytidostea is a clade of stereospondyl temnospondyls. It was erected in 2000 to include several temnospondyl groups distinct from the "higher" group of capitosaurs, including lydekkerinids, brachyopoids, and rhytidosteids. Rhytidosteans first appeared in the Permian period and underwent an evolutionary radiation during the Induan stage of the Early Triassic. Along with capitosaurs, rhytidosteans comprise much of the larger suborder Stereospondyli. Rhytidostea has often been considered the sister group of the clade Capitosauria, but has been placed in various other phylogenetic positions. In many studies, members of Rhytidostea are split, with lydekkerinids having a more basal position among stereospondyls while rhytidosteids and brachyopoids form a group placed among the more derived trematosaurian stereospondyls.
Schoch and Milner (2000) erected the clade Rhytidostea to include lydekkerinids, brachyopoids, and rhytidosteids. The clade was the sister taxon of Capitosauria, the "higher" stereospondyls. Ruta et al. (2007) placed Rhytidostea in a similar phylogenetic position, defining it as a clade including Eolydekkerina (a lydekkerinid), Batrachosuchus (a brachyopid), and all descendants of their most recent common ancestor. Below is a cladogram modified from Ruta et al. (2007): [1]
Stereospondyli |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Other phylogenetic analyses have placed rhytidosteids and brachyopoids as closely related groups within Trematosauria, a more derived clade of stereospondyls. [2] [3] They are separate from the lydekkerinids, which remain a basal group of stereospondyls.
Temnospondyli is a diverse order of small to giant tetrapods—often considered primitive amphibians—that flourished worldwide during the Carboniferous, Permian, and Triassic periods. A few species continued into the Cretaceous. Fossils have been found on every continent. During about 210 million years of evolutionary history, they adapted to a wide range of habitats, including fresh water, 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 considered amphibians, many had characteristics, such as scales, claws, and armour-like bony plates, that distinguish them from modern amphibians.
Dvinosaurs are one of several new clades of Temnospondyl amphibians named in the phylogenetic review of the group by Yates and Warren 2000. They represent a group of primitive semi-aquatic to completely aquatic amphibians, and are known from the Late Carboniferous to the Early Triassic, being most common in the Permian period. Their distinguishing characteristics are a reduction of the otic notch; the loss of a flange on the rear side of the pterygoid; and 28 or more presacral vertebrae.
Trematosauria is one of two major groups of temnospondyl amphibians that survived the Permian-Triassic extinction event, the other being the Capitosauria. The trematosaurs were a diverse and important group that included many medium-sized to large forms that were semi-aquatic to totally aquatic. The group included long-snouted forms such as the trematosauroids and short, broad-headed forms such as the metoposaurs. Although most groups did not survive beyond the Triassic, one lineage, the brachyopoids, continued until the Cretaceous period. Trematosauria is defined as all stereospondyls more closely related to Trematosaurus than to Parotosuchus, a capitosaurian.
The Stereospondyli are a group of extinct temnospondyl amphibians that existed primarily during the Mesozoic period. They are known from all seven continents and were common components of many Triassic ecosystems, likely filling a similar ecological niche to modern crocodilians prior to the diversification of pseudosuchian archosaurs.
Brachyopoidea is a superfamily of temnospondyls that lived during the Mesozoic. It contains the families Brachyopidae and Chigutisauridae. The earliest records of brachyopids are from the Lower Triassic in Australia. The latest-surviving member of the superfamily is the chigutisaurid Koolasuchus from the Early Cretaceous of Australia.
Lydekkerinidae is a family of stereospondyl temnospondyls that lived in the Triassic period. During the Triassic, lydekkerinids had a global distribution. They were small-bodied with wedge-shaped, roughly triangular heads. Fossils have been found in Russia, Greenland, India, South Africa, Madagascar, and Australia. The type genus is Lydekkerina, the namesake of the family and the most well-known lydekkerinid.
Limnarchia is a clade of temnospondyls. It includes the mostly Carboniferous-Permian age Dvinosauria and the mostly Permian-Triassic age Stereospondylomorpha. The clade was named in a 2000 phylogenetic analysis of stereospondyls and their relatives. Limnarchia means "lake rulers" in Greek, in reference to their aquatic lifestyles and long existence over a span of approximately 200 million years from the Late Carboniferous to the Early Cretaceous. In phylogenetic terms, Limnarchia is a stem-based taxon including all temnospondyls more closely related to Parotosuchus than to Eryops. It is the sister group of the clade Euskelia, which is all temnospondyls more closely related to Eryops than to Parotosuchus. Limnarchians represent an evolutionary radiation of temnospondyls into aquatic environments, while euskelians represent a radiation into terrestrial environments. While many euskelians were adapted to life on land with strong limbs and bony scutes, most limnarchians were better adapted for the water with poorly developed limbs and lateral line sensory systems in their skulls.
Almasaurus is an extinct genus of trematosaurian temnospondyl within the family Latiscopidae. It is known from several skulls and some postcranial material found from the Argana Formation in Morocco, which dates back to the Late Triassic.
Bothriceps is an extinct genus of stereospondyl temnospondyl. It is a member of the infraorder Trematosauria and is the most basal brachyopomorph known. It is one of the only brachyopomorph that lies outside the superfamily Brachyopoidea, which includes the families Brachyopidae and Chigutisauridae. It shares several similarities to Keratobrachyops, another basal brachyopomorph, and may be closely related to or even synonymous with it.
Lapillopsis is an extinct genus of stereospondyl temnospondyl within the family Lapillopsidae. Fossils belonging to the genus have been found in the Arcadia Formation of Queensland, Australia.
Keratobrachyops is an extinct genus of trematosaurian temnospondyl found in the Arcadia Formation of Queensland, Australia. It had been thought to be a basal chigutisaurid but is now thought to be a basal brachyopomorph closely related to the genus Bothriceps, and may even be a synonym of it.
Rileymillerus is an extinct genus of temnospondyl amphibian from the Late Triassic Post Quarry in the Dockum Group of Texas that was described by John Bolt and Sankar Chatterjee in 2000. The holotype, a nearly complete skull with articulated jaws, is housed at the Museum of Texas Tech University. The genus is named for Riley Miller, who allowed Chatterjee to work on the Post Quarry, and the species is named for the paleontologist John Cosgriff.
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.
Capitosauria is an extinct group of large temnospondyl amphibians with simplified stereospondyl vertebrae. Mainly living as piscivores in lakes and rivers, the Capitosauria and its sister taxon Trematosauria were the only major labyrinthodonts that existed during the Mesozoic in ecological niches broadly similar to those of modern crocodiles, and some grew to very large sizes. At 6 meter in length, the Mid-Triassic Mastodonsaurus giganteus is not only thought to have been the largest capitosaur, but possibly also the largest amphibian to have lived. The latest known remains are from the Rhaetian of Germany and are referred to Cyclotosaurus.
Stenotosauridae is an extinct family of mastodonsauroid temnospondyls. It has included genera such as Stenotosaurus, Wellesaurus, and Procyclotosaurus.
Nanolania is an extinct genus of rhytidosteid temnospondyl from the early Triassic period of south central Queensland, Australia. It is known from the holotype QMF 12293, a postorbital fragment associated with lower jaw fragments and from the associated paratypes QMF 14480, a laterally complete skull with mandibles, QMF 35247, a poorly preserved skull with right mandibular ramus, QMF 35393, a badly preserved partial skull and QMF 39666, a posterior orbital and mandibular fragment, recovered from the Arcadia Formation in the Rewan Group. This genus was named by Adam M. Yates in 2000, and the type species is Nanolania anatopretia.
Derwentiinae is a subfamily of rhytidosteid temnospondyls from the Permian and Triassic periods of Australia and India. It includes the genera Arcadia, Deltasaurus, Derwentia, Indobrachyops, and Rewana. Derwentiinae was named in a 2011 study that analyzed the phylogenetic relationships of rhytidosteids. It was a replacement name for the family Derwentiidae, which was named in 2000.
Vigilius is an extinct genus of brachyopid temnospondyl amphibian from the Triassic of Arizona. It is known from the single type species Vigilius wellesi.
Manubrantlia was a genus of lapillopsid from the Early Triassic Panchet Formation of India. This genus is only known from a single holotype left jaw, given the designation ISI A 57. Despite the paucity of remains, the jaw is still identifiable as belonging to a relative of Lapillopsis. For example, all three of its coronoid bones possessed teeth, the articular bone is partially visible in lateral (outer) view, and its postsplenial does not contact the posterior meckelian foramen. However, the jaw also possesses certain unique features which justify the erection of a new genus separate from Lapillopsis. For example, the mandible is twice the size of any jaws referred to other lapillopsids. The most notable unique feature is an enlarged "pump-handle" shaped arcadian process at the back of the jaw. This structure is responsible for the generic name of this genus, as "Manubrantlia" translates from Latin to the English expression "pump-handle". The type and only known species of this genus is Manubrantlia khaki. The specific name refers to the greenish-brown mudstones of the Panchet Formation, with a color that had been described as "khaki" by the first British geologists who studied the formation.
Latiscopus disjunctus is a small Late Triassic temnospondyl collected in 1940 by a Works Projects Administration crew working near Otis Chalk, Texas that was described by John Wilson in 1948.