Doleserpeton | |
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Scientific classification | |
Kingdom: | Animalia |
Phylum: | Chordata |
Order: | † Temnospondyli |
Family: | † Amphibamidae |
Genus: | † Doleserpeton |
Species: | †D. annectens |
Binomial name | |
†Doleserpeton annectens Bolt, 1969 | |
Doleserpeton is an extinct, monospecific genus of dissorophoidean temnospondyl within the family Amphibamidae that lived during the Upper Permian, 285 million years ago. [1] Doleserpeton is represented by a single species, Doleserpeton annectens, which was first described by John R. Bolt in 1969. [2] Fossil evidence of Doleserpeton was recovered from the Dolese Brothers Limestone Quarry in Fort Sill, Oklahoma. [3] The genus name Doleserpeton is derived from the initial discovery site in Dolese quarry of Oklahoma and the Greek root "serp-", meaning "low or close to the ground". This transitional fossil displays primitive traits of amphibians that allowed for successful adaptation from aquatic to terrestrial environments. In many phylogenies, lissamphibians appear as the sister group of Doleserpeton. [4]
There was only one successful excavation of the genus Doleserpeton, which was during the initial discovery in 1969 by Bolt and his colleagues in Fort Sill, Oklahoma. The stratigraphic location of Doleserpeton was based in Fissure Fills and the Admirial Formation, which was dated back to the Upper Permian. [5] All fossil specimens were preserved in limestone blocks, which was treated with an acid wash to clear away excess debris and minimize damage during the excavation process. The following fossil evidence of Doleserpeton was retrieved:
The skull is broad, rounded, and flat, and was estimated to be approximately 15mm but could reach a length of 19mm. Skull features of Doleserpeton included a deepened otic notch and expanded interpterygoid vacuities and vomers. [6] The eye orbits in Doleserpeton are relatively large in proportion to the overall size of its skull. Inner ear characteristics of Doleserpeton share morphological similarities to salamanders in the otic region, in which the tympanum is not connected to the stapes. [7]
The distinguishing synapomorphy that defines Doleserpeton are its bicuspid, pedicellate teeth. Each bicuspid, pedicellate tooth in Doleserpeton had two cusps with a separation from the root by a region of uncalcified fibrous tissue. The uncalcified regions of the bicuspid teeth in Doleserpeton were often lost and replaced during its lifetime to support a carnivorous diet. The maxilla contained 60 bicuspid, pedicellate teeth, in which 40 teeth were located in the upper jaw and 20 teeth were located in the lower jaw. Doleserpeton contained marginal teeth located on the premaxilla and palatal bones of the skull. It was hypothesized that Doleserpeton contained a range of 22-25 marginal teeth.
Doleserpeton possessed a rhachitomous vertebrae, in which the pleurocentrum dominates in size in each vertebra compared to the intercentrum. [1] This "rhachitomous" vertebrae is unique to amphibians and its relatives, which is one of the defining traits of Doleserpeton and its relatives. Doleserpeton contained 10 vertebrae in its cervical column, 24 presacral vertebrae, 2 sacral vertebrae, and an estimate of 15 caudal vertebrae that was concluded from fossil evidence. Rib attachment started at the second presacral vertebrae and continue throughout the length of its body until the sacral vertebrae. Rib size increased from ribs 2 through 4, and the decreased in size after the fifth presacral vertebrae. Ribs were double headed to allow a sturdy attachment for muscles to support its body mass on land.
Doleserpeton displayed a sprawling posture, in which locomotion was achieved on all four limbs while dragging part of its midsection on the ground. Sprawling posture is considered the most primitive trait of terrestrial locomotion, which is consistent with the evolutionary trend from aquatic to terrestrial adaptations. Sprawling posture allowed Doleserpeton to possess the stability and functionality to move on land while also being efficient and functional in aquatic environments.
The development in pectoral girdle elements as well as pelvic girdle elements in Doleserpeton displayed the shift in traits that supported amphibious adaptions to aquatic and terrestrial environments. Limb structures of Doleserpeton were homologous to temnospondyli and to other derived terrestrial species. [8] The prominence of the scapulocoracoid in the pectoral girdle ofDoleserpeton allowed them to move efficiently on land while supporting the upper half of its body. The humerus is and attached perpendicularly to the scauplcorcoid. The carpals, metacarpals, and digits of Doleserpeton were allowed for full mobility of its forelimbs and joints to travel on land while providing adequate support for its body mass and size. [9]
The pelvic girdle also displays the same characteristics as the pectoral girdle. The femur is elongated and enlarged and place perpendicularly to the pelvic girdle. The proximal end of the femur was enlarged to allow strong muscle attachment and also displayed well developed tarsals, metatarsals, and phalanges that served the same purposes for mobility and flexibility of joints in their hindlimbs.
The digit formula for Doleserpeton is 4 digits on the forelimbs and 5 digits on the hindlimb. This digit formula is primitive to all living amphibians with a few exceptions in Caecilian and some outlying amphibious species.
Parsimony-based cladistic analysis and Bayesian inference analysis were utilized to analyze 20 taxa and 51 characters to classify Doleserpeton. [2] Finite classification of Doleserpeton still remain dubious because of the uncertainty of the phylogenetic classification of the family Amphibamidae and the subclass Lissamphibia. The classification of the family Amphibamidae is based on the notion that the origin of Lissamphibia is derived from three hypotheses, which conflicts with the evolutionary position of Doleserpeton in relation to its primitive ancestors and descendants. [10] Three hypotheses of Lissamphibia classification are pose three possibilities of Lissamphibia origin:
The most parsimonious tree showed that Doleserpeton is loosely classified as the sister group to the genus Amphimabus within the family Amphibamidae. Character traits that support this phylogenetic classification include the following synapomorphies: bicuspid teeth, morphological similarities in larval stages, and separation between the crown and base of the tooth in its pedicellate dentition. [2]
Physical characteristics from fossil evidence of Doleserpeton indicate that they resembled modern newts and salamanders. [2] The overall size of Doleserpeton was relatively small, with an estimated body length of 55 mm (2.165 inches) from snout to tail. Morphological features of Doleserpeton indicated that they were quadrupedal with elongate bodies and a lizard-like appearance. Their overall body morphology included short limbs protruding from a 90-degree angle, long tails, and flattened skulls with blunt snouts. Doleserpeton may have had smooth, granular skin to adapt to the transition from aquatic to terrestrial environments. [2] Fossil evidence and classification of Doleserpeton predicted that they transitioned through metamorphic stages throughout their life, but lived primarily on terrestrial land during juvenile and adult stages. Like their modern amphibious relatives Lissamphibia, Doleserpeton may have had to rely on the availability of a nearby water source during reproduction and larval stages.
The skeletal elements from fossil evidence were well ossified, which supported the notion that Doleserpeton lived a primarily terrestrial life after metamorphosis. A well ossified skeletal structure in Doleserpeton indicated the lack of maturity in several Doleserpeton specimens. The ossification process in Doleserpeton deviates from typical terrestrial skeletal ossification, in which well ossified skeletal elements were indicators of maturity in terrestrial organisms. Variation in ossification in fossil specimens of Dolserpeton infer the possibility of skeletal changes in adult stages in life, concluding that the fossil evidence can only support characteristics that would define skeletal elements and characteristics only up to juvenile stages.
The Lissamphibians are a group of tetrapods that includes all modern amphibians. Lissamphibians consist of three living groups: the Salientia, the Caudata, and the Gymnophiona. A fourth group, the Allocaudata, was moderately successful, spanning 160 million years from the Middle Jurassic to the Early Pleistocene, but became extinct 2 million years ago.
Eryops meaning "drawn-out face" because most of its skull was in front of its eyes is a genus of extinct, amphibious temnospondyls. It contains the single species Eryops megacephalus, the fossils of which are found mainly in early Permian rocks of the Texas Red Beds, located in Archer County, Texas. Fossils have also been found in late Carboniferous period rocks from New Mexico. Several complete skeletons of Eryops have been found in lower Permian rocks, but skull bones and teeth are its most common fossils.
Labyrinthodontia is an extinct amphibian subclass, which constituted some of the dominant animals of late Paleozoic and early Mesozoic eras. The group evolved from lobe-finned fishes in the Devonian and is ancestral to all extant landliving vertebrates. As such it constitutes an evolutionary grade rather than a natural group (clade). The name describes the pattern of infolding of the dentin and enamel of the teeth, which are often the only part of the creatures that fossilize. They are also distinguished by a heavily armoured skull roof, and complex vertebrae, the structure of which were used in older classifications of the group.
Lepospondyli is a diverse taxon of amphibian tetrapods. With the exception of one late-surviving lepospondyl from the Late Permian of Morocco, lepospondyls lived from the Early Carboniferous (Mississippian) to the Early Permian and were geographically restricted to what is now Europe and North America. Five major groups of lepospondyls are known: Adelospondyli; Aïstopoda; Lysorophia; Microsauria; and Nectridea. Lepospondyls have a diverse range of body forms and include species with newt-like, eel- or snake-like, and lizard-like forms. Various species were aquatic, semiaquatic, or terrestrial. None were large, and they are assumed to have lived in specialized ecological niches not taken by the more numerous temnospondyl amphibians that coexisted with them in the Paleozoic. Lepospondyli was named in 1888 by Karl Alfred von Zittel, who coined the name to include some tetrapods from the Paleozoic, that shared some specific characteristics in the notochord and teeth. Lepospondyls have sometimes been considered to be either related or ancestral to modern amphibians or to Amniota.
Cacops, a genus of dissorophid temnospondyls, is one of the most distinctive Paleozoic amphibians that diversified in the equatorial region of Pangea during the Kungurian stage of the early Permian. Dissorophids were a group of fully terrestrial, often heavily armored faunivores. This, along with their relatively large size and geographical range suggest that they were able to coexist with amniotes as predators during the early Permian. Dissorophidae has four distinct clades differentiated largely on the morphology of the osteoderms, the Eucacopinae, the Dissorophinae, the Aspidosaurinae, and the Platyhystricinae. Cacops is one of the few olsoniforms whose ontogeny is beginning to surface. Cacops fossils were almost exclusively known from the Cacops Bone Bed of the Lower Permian Arroyo Formation of Texas for much of the 20th century. New material collected from the Dolese Brothers Quarry, near Richards Spur, Oklahoma in the past few decades has been recovered, painting a clearer picture of what the animal looked and acted like.
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 Jurassic and Cretaceous periods. 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.
Petrolacosaurus is an extinct genus of diapsid reptile from the late Carboniferous period. It was a small, 40-centimetre (16 in) long reptile, and the earliest known reptile with two temporal fenestrae. This means that it was at the base of Diapsida, the largest and most successful radiation of reptiles that would eventually include all modern reptile groups, as well as dinosaurs and other famous extinct reptiles such as plesiosaurs, ichthyosaurs, and pterosaurs. However, Petrolacosaurus itself was part of Araeoscelida, a short-lived early branch of the diapsid family tree which went extinct in the mid-Permian.
Scutosaurus was a genus of parareptiles. It was an armor-covered pareiasaur that lived around 265–254 million years ago in Russia, in the later Permian period. Its genus name refers to large plates of armor scattered across its body. It was a large anapsid reptile that, unlike most reptiles, held its legs underneath its body to support its great weight. Fossils have been found in the Sokolki Assemblage Zone of the Malokinelskaya Formation in European Russia, close to the Ural Mountains.
Casea is an extinct genus of medium to large-bodied, herbivorous, pelycosaur synapsids from the late Carboniferous until the middle Permian. The name Casea references its appearance from the Caseasauria which developed new morphology of their external naris and snout. Casea were known to be about 1.2 meters long. It weighed between 150 kg to 200 kg. It was slightly smaller than the otherwise very similar Caseoides. Casea was one of the first amniote herbivores, sharing its world with animals such as Dimetrodon and Eryops. It was possibly also aquatic.
Tulerpeton is an extinct genus of Devonian four-limbed vertebrate, known from a fossil that was found in the Tula Region of Russia at a site named Andreyevka. This genus and the closely related Acanthostega and Ichthyostega represent the earliest tetrapods.
Gerobatrachus is an extinct genus of amphibamid temnospondyl that lived in the Early Permian, approximately 290 million years ago (Ma), in the area that is now Baylor County, Texas. When it was first described in 2008, Gerobatrachus was announced to be the closest relative of Batrachia, the group that includes modern frogs and salamanders. It possesses a mixture of characteristics from both groups, including a large frog-like head and a salamander-like tail. These features have led to it being dubbed a frogamander by the press. Some more recent studies place Gerobatrachus as the closest relative of Lissamphibia, the group that contains all modern amphibians including frogs, salamanders, and caecilians, or place modern amphibians far from Gerobatrachus within a group called Lepospondyli.
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Tersomius is an extinct genus of dissorophoid temnospondyl within the family Micropholidae. It is known from the early Permian of North America.
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This list of fossil amphibians described in 2020 is a list of new taxa of fossil amphibians that were described during the year 2020, as well as other significant discoveries and events related to amphibian paleontology that occurred in 2020.