Lydekkerina Temporal range: Early Triassic | |
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Life restoration of Lyddekerina huxleyi | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Amphibia |
Order: | † Temnospondyli |
Suborder: | † Stereospondyli |
Family: | † Lydekkerinidae |
Genus: | † Lydekkerina Broom, 1915 |
Species | |
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Synonyms [1] | |
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Lydekkerina is an extinct genus of stereospondyl temnospondyl. It is the type genus of the family Lydekkerinidae. Fossils have been collected from Early Triassic deposits in South Africa and Australia. The type species is L. huxleyi , first described in 1889. While most other stereospondyls were semiaquatic, Lydekkerina was exclusively terrestrial. [2] [3]
Lydekkerina was a relatively small temnospondyl, growing up to around 1 metre (3.3 ft) in length. [3] Skulls range in length from 49 millimetres (1.9 in) in the smallest known individual to up to 100 millimetres (3.9 in) in larger individuals. [4] [3] The skull is wedge-shaped and has a parabolic outline with convex lateral margins. Shallow pits cover the surface of the skull. Teeth line the palate as well as the jaws, and some skulls even bear large ectopterygoid tusks on the underside of the skull. [3]
Lydekkerina can be distinguished from other lydekkerinids on the basis of several skull characteristics. One such feature is the presence of vomerine shagreen, tiny bumps covering the bones of the palate. An opening at the tip of the palate called the anterior palatal vacuity is divided by two projections of the skull roof, a second distinctive feature of the genus. Moreover, distinctive ridges are present on the underside of the skull roof around the eye sockets, probably to provide structural support. [3] [5]
Lydekkerina huxleyi was first briefly described as a species of Bothriceps by Richard Lydekker in 1889. The specific name honors Thomas Henry Huxley, an English biologist who named the genus Bothriceps in 1859 from material in Australia. [6] Robert Broom, a South African paleontologist, provided a more accurate description of the species in 1915 and reassigned it to the new genus Lydekkerina, named after Lydekker. [7] The type specimen and a paratype specimen were described in much greater detail, particularly the lower jaw, in 2007 by R. Hewison, and a detailed account of its sacral region, pelvic girdle and hind limb.
Lydekkerina is one of the most common temnospondyls found from the Permo-Triassic Karoo Basin of South Africa. Many fossils have been found from the Lystrosaurus Assemblage Zone of the Beaufort Group. Many, however, are poorly preserved, being crushed or deformed. The variable conditions of specimens has resulted in confusion in identification. Some paleontologists have proposed that variations in skull shape among specimens represent deformities rather than true morphologies. Therefore, characteristics that distinguish different lydekkerinids from one another may be the results of preservation, not taxonomic distinctness. In 2006, it was proposed that the South African lydekkerinids Limnoiketes and Broomulus were synonymous with Lydekkerina for this reason. [3]
A second species of Lydekkerina, L. putterilli, was named by Broom in 1930. [8] Its description was based on a small partial skull from the Permian Dicynodon Assemblage Zone. It was later considered to be a juvenile rhinesuchid related to Uranocentrodon . [9] In 2000, L. putterilli was assigned to its own genus, Broomistega . [4]
Broom described a third species, L. kitchingi, from the Dicynodon Assemblage Zone in 1950. [10] In 1996 it was reassigned as a juvenile form of the rhinesuchid Muchocephalus . [11] In 2003, both L. kitchingi and Muchocephalus were synonymized with Laccosaurus . [12]
Temnospondyl remains from the Early Triassic Rewan Formation of Queensland, Australia, were described in 2006 and assigned to Lydekkerina huxleyi. These remains possess characters diagnostic of Lydekkerina such as the ridges underneath the skull roof and the vomerine shagreen. [5]
Because the bones of Lydekkerina are more heavily ossified than other stereospondyls, it is thought to have been terrestrial. [2] Large bony projections on the skeleton likely served as attachments for strong muscles. Joints between bones were well-developed, enabling effective locomotion on land. The sensory system of pressure-sensitive sulci across the skull is poorly developed, suggesting that Lydekkerina had little use for these organs in a land environment. [3] The skeleton of Lydekkerina is similar to those of early stereospondyl relatives such as the archegosauroids, but bears little resemblance to those of the exclusively terrestrial Permian temnospondyls. [2]
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 armour-like bony plates that distinguish them from the modern soft-bodied lissamphibians.
Rhinesuchus is a large temnospondyl. Remains of the genus are known from the Permian of the South African Karoo Basin's Tapinocephalus and Cistecephalus assemblage zones, both belonging to the Beaufort Group. The skull of Rhinesuchus had a flat triangular shape with blunt snout similar to some of the other large temnospondyls, and had a palate filled with small sharp teeth, suggesting that it hunted fish. Also, the small eyes were on top of the head suggesting that it approached its prey from below.
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.
Eryosuchus is an extinct genus of capitosauroid temnospondyl from the Middle Triassic of northern Russia. It was a very large predator: the largest specimen known could reach up to 3.5 m (11.5 ft) in length, with a skull over 1 m long.
Uranocentrodon is an extinct genus of temnospondyls in the family Rhinesuchidae. Known from a 50 centimetres (20 in) skull, Uranocentrodon was a large predator with a length up to 3.75 metres (12.3 ft). Originally named Myriodon by van Hoepen in 1911, it was transferred to a new genus on account of the name being preoccupied in 1917. It has been synonymized with Rhinesuchus, but this has not been widely supported. It was also originally considered to be of Triassic age, but more recent analysis has placed its age as just below the Permian-Triassic boundary.
Trematosaurus is an extinct genus of trematosaurid temnospondyl amphibian found in Germany and Russia. It was first named by Hermann Burmeister in 1849 and the type species is Trematosaurus brauni.
Australerpeton is an extinct genus of stereospondylomorph temnospondyl currently believed to belong to the family Rhinesuchidae. When first named in 1998, the genus was placed within the new family Australerpetontidae. However, studies published a few years later questioned the systematics used in the original description and included the genus within Archegosauridae. A study by Dias & Schultz (2003) reassigned Australerpeton to the family Rhinesuchidae within the suborder Stereospondyli based on an earlier evaluation of the family. In this study, the close similarities between Australerpeton and archegosaurids were attributed to convergent evolution as a result of similar semi-aquatic lifestyles. A redescription of the skeleton of this genus was published by Eltink & Langer in 2014, and the skull was redescribed in a follow-up study published by Eltink et al. in 2016. These studies, as well as a 2017 study focusing on rhinesuchids in general, confirmed that Australerpeton was a rhinesuchid rather than an archegosaurid. Fossils of the genus have been found in the Rio do Rasto Formation of Brazil.
Rhinesuchidae is a family of tetrapods that lived primarily in the Permian period. They belonged to the broad group Temnospondyli, a successful and diverse collection of semiaquatic tetrapods which modern amphibians are probably descended from. Rhinesuchids can be differentiated from other temnospondyls by details of their skulls, most notably the interior structure of their otic notches at the back of the skull. They were among the earliest-diverging members of the Stereospondyli, a subgroup of temnospondyls with flat heads and aquatic habits. Although more advanced stereospondyls evolved to reach worldwide distribution in the Triassic period, rhinesuchids primarily lived in the high-latitude environments of Gondwana during the Guadalupian and Lopingian epochs of the Permian. The taxonomy of this family has been convoluted, with more than twenty species having been named in the past; a 2017 review recognized only eight of them to be valid. While several purported members of this group have been reported to have lived in the Triassic period, most are either dubious or do not belong to the group. However, at least one valid genus of rhinesuchid is known from the early Triassic, a small member known as Broomistega. The most recent formal definition of Rhinesuchidae, advocated by Mariscano et al. (2017) is that of a stem-based clade containing all taxa more closely related to Rhinesuchus whaitsi than to Lydekkerina huxleyi or Peltobatrachus pustulatus. A similar alternate definition is that Rhinesuchidae is a stem-based clade containing all taxa more closely related to Uranocentrodon senekalensis than to Lydekkerina huxleyi, Trematosaurus brauni, or Mastodonsaurus giganteus.
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.
Microposaurus is an extinct genus of trematosaurid temnospondyl. Fossils are known from the Cynognathus Assemblage Zone of the Beaufort Group in South Africa and the Rouse Hill Siltstone of Australia that date back to the Anisian stage of the Middle Triassic. These aquatic creatures were the short snouted lineage from Trematosaurinae.
Broomistega is an extinct genus of temnospondyl amphibian in the family Rhinesuchidae. It is known from one species, Broomistega putterilli, which was renamed in 2000 from Lydekkerina putterilli Broom 1930. Fossils are known from the Early Triassic Lystrosaurus Assemblage Zone of the Beaufort Group in the Karoo Basin of present-day South Africa, a region that had been an enclave of Gondwana. Specimens of B. putterilli were once thought to represent young individuals of another larger rhinesuchid such as Uranocentrodon, but the species is now regarded as a paedomorphic taxon, possessing the features of juvenile rhinesuchids into adulthood.
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.
Cryobatrachus is an extinct genus of temnospondyl amphibian from the Early Triassic of Antarctica. The type species is Cryobatrachus kitchingi. It is known from a partial skull and an imprint of the skull roof, both found in the Fremouw Formation of the Transantarctic Mountains at about 85° south latitude and described in 1974. Many small bone fragments have also been identified, although they cannot be attributed with certainty to C. kitchingi. Cryobatrachus has been classified in the family Lydekkerinidae, as it is similar in appearance to the genus Lydekkerina from South Africa. Because only a small number of features distinguish it from other lydekkerinids, Cryobatrachus kitchingi has more recently been considered a nomen dubium, meaning that its distinction from other better-known species may be unwarranted.
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.
Laccosaurus is an extinct monotypic genus of rhinesuchid temnospondyl, the type species being Laccosaurus watsoni.
Rhineceps is an extinct genus of temnospondyl amphibian in the family Rhinesuchidae. Rhineceps was found in Northern Malawi in Southern Africa known only from its type species R. nyasaensis. Rhineceps was a late Permian semi-aquatic carnivore that lived in streams, rivers, lakes or lagoons. Rhineceps is an early divergent Stereopondyl within the family Rhinesuchidae, which only existed in the late Permian (Lopingian) and failed to survive the Permian-Triassic extinction unlike other stereospondyl families.
Arachana is an extinct genus of rhinesuchid-like temnospondyl known from the Early Triassic Buena Vista Formation of northeastern Uruguay. Arachana was first named by Graciela Piñeiro, Alejandro Ramos and Claudia Marsicano in 2012 and the type species is A. nigra. It shares characteristics with both rhinesuchids and lydekkerinids, making it a transitional form between basal and more advanced stereospondyls.
Pelictosuchus is an extinct genus of therocephalian therapsids from the Late Permian of South Africa. It is classified in the family Akidnognathidae. The type species Pelictosuchus paucidens was named by South African paleontologist Robert Broom in 1940 from the Dicynodon Assemblage Zone.
Eolydekkerina is an extinct genus of temnospondyl from the Early Triassic of South Africa. It belongs to the family Lydekkerinidae, along with the closely related genus Lydekkerina. It is known from a single type species, Eolydekkerina magna, which was named in 1996 from a part of the Beaufort Group called the Lystrosaurus Assemblage Zone.
Manubrantlia was a genus of lapillopsid temnospondyls 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.