Altenglanerpeton Temporal range: Late Carboniferous or Early Permian, | |
---|---|
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Order: | † Microsauria |
Clade: | † Recumbirostra |
Genus: | † Altenglanerpeton Glienke, 2012 |
Type species | |
†Altenglanerpeton schroederi Glienke, 2012 |
Altenglanerpeton is an extinct genus of microsaur tetrapod from the Late Carboniferous or Early Permian of Germany. [1] Altenglanerpeton was named in 2012 after the Altenglan Formation in which it was found. The type and only species is A. schroederi.
Altenglanerpeton is known from a single partial skeleton from an outcrop of the Altenglan Formation, which is part of the Saar–Nahe Basin. The Altenglan Formation dates back to the Carboniferous-Permian transition, about 299 million years ago. The skeleton was discovered sometime in the 1870s in the village of Werschweiler, and was first described by German paleontologist Eckart Schröder in 1939. [2] Schröder tentatively assigned the specimen to the microsaur Microbrachis , although its classification as a microsaur was questioned in later years. [1]
The holotype skeleton includes a crushed skull preserved in dorsal or top view, and a straight length of vertebrae and associated ribs that are poorly preserved. The forelimbs and parts of the pectoral girdle are also preserved. The hind limbs and tail are missing. Altenglanerpeton has a robust skull with small, widely spaced eye sockets. The skull appears triangular from above as well as from the side, since it has a narrow and pointed snout. One distinguishing feature of Altenglanerpeton is the extension of the jugal bones far in front of the eye sockets. Unlike many other microsaurs, Altenglanerpeton lacks a network of lateral line grooves across its skull. Altenglanerpeton has an elongated body with around 30 simple spool-shaped vertebrae and small, poorly developed limbs. It is similar in appearance to the ostodolepids Micraroter and Pelodosotis , both of which have long bodies and tiny limbs. [1]
Altenglanerpeton belongs to a group of early amphibians called microsaurs, characterized by their small size and simple vertebrae. When Altenglanerpeton was first named in 2012, a phylogenetic analysis was conducted to determine its relationship with other lepospondyls. In support of Schröder's original assignment, Altenglanerpeton was placed as a microsaur. "Microsauria" is now considered to be a paraphyletic grouping, meaning that it does not form a true clade. Altenglanerpeton belongs to a similar group called Recumbirostra, which is a clade. Altenglanerpeton was found to be most closely related to Tambaroter , named in 2011 from the Early Permian Tambach Formation of Germany. According to the analysis, Altenglanerpeton and Tambaroter form a clade that is the sister taxon to the family Brachystelechidae. Altenglanerpeton is most similar in appearance to ostodolepids, and although both are members of Recumbirostra, Ostodolepidae is only distantly related to Altenglanerpeton. Below is a cladogram showing the phylogenetic position of Altenglanerpeton from Glienke (2012): [1]
The layer of the Altenglan Formation in which Altenglanerpeton was found is thought to have been deposited in a lake environment, specifically that of Hauptkalk Lake, a large, shallow body of water that covered much of the Saar–Nahe Basin at the Carboniferous-Permian transition. Sedimentation rates in the lake were low, meaning that few fossils were preserved. Besides the Altenglanerpeton skeleton, only three tetrapod fossils are known from Hauptkalk Lake deposits: two specimens of the temnospondyl Apateon pedestris and a skull of the temnospondyl Sclerocephalus bavaricus . The microsaur Batropetes is also known from the Saar-Nahe Basin, but it comes from the younger Odernheim Subformation. [1]
The presence of Altenglanerpeton in a lake deposit suggests that it was aquatic. The long body and reduced limbs would have facilitated lateral undulation as a form of swimming. Although it is not preserved in the holotype specimen, the tail may have had an elongated tadpole-like fin. In contrast, the robust skull and lack of lateral line grooves in Altenglanerpeton suggest that it was primarily terrestrial. While most aquatic amphibians have large, forward-facing eyes and three-dimensional vision for capturing prey underwater, Altenglanerpeton has small, laterally-directed eyes that would have been more suitable for burrowing, as in living caecilians. With its elongated body, Altenglanerpeton may have undulated through soil and leaf litter. [1]
"Labyrinthodontia" is an informal grouping of extinct predatory amphibians which were major components of ecosystems in the late Paleozoic and early Mesozoic eras. Traditionally considered a subclass of the class Amphibia, modern classification systems recognize that labyrinthodonts are not a formal natural group (clade) exclusive of other tetrapods. Instead, they consistute an evolutionary grade, ancestral to living tetrapods such as lissamphibians and amniotes. "Labyrinthodont"-grade vertebrates evolved from lobe-finned fishes in the Devonian, though a formal boundary between fish and amphibian is difficult to define at this point in time.
Lepospondyli is a diverse taxon of early tetrapods. With the exception of one late-surviving lepospondyl from the Late Permian of Morocco, lepospondyls lived from the Visean stage of the Early Carboniferous 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. It has been suggested that the grouping is polyphyletic, with aïstopods being primitive stem-tetrapods, while recumbirostran microsaurs are primitive reptiles.
Adelospondyli is an order of elongated, presumably aquatic, Carboniferous amphibians. They have a robust skull roofed with solid bone, and orbits located towards the front of the skull. The limbs were almost certainly absent, although some historical sources reported them to be present. Despite the likely absence of limbs, adelospondyls retained a large part of the bony shoulder girdle. Adelospondyls have been assigned to a variety of groups in the past. They have traditionally been seen as members of the subclass Lepospondyli, related to other unusual early tetrapods such as "microsaurs", "nectrideans", and aïstopods. Analyses such as Ruta & Coates (2007) have offered an alternate classification scheme, arguing that adelospondyls were actually far removed from other lepospondyls, instead being stem-tetrapod stegocephalians closely related to the family Colosteidae.
Reptiliomorpha is a clade containing the amniotes and those tetrapods that share a more recent common ancestor with amniotes than with living amphibians (lissamphibians). It was defined by Michel Laurin (2001) and Vallin and Laurin (2004) as the largest clade that includes Homo sapiens, but not Ascaphus truei. Laurin and Reisz (2020) defined Pan-Amniota as the largest total clade containing Homo sapiens, but not Pipa pipa, Caecilia tentaculata, and Siren lacertina.
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.
Microbrachis is an extinct genus of microsaurian tetrapod from the Carboniferous Kladno Formation of the Czech Republic.
Nectridea is the name of an extinct order of lepospondyl tetrapods from the Carboniferous and Permian periods, including animals such as Diplocaulus. In appearance, they would have resembled modern newts or aquatic salamanders, although they are not close relatives of modern amphibians. They were characterized by long, flattened tails to aid in swimming, as well as numerous features of the vertebrae.
Cotylorhynchus is an extinct genus of herbivorous caseid synapsids that lived during the late Lower Permian (Kungurian) and possibly the early Middle Permian (Roadian) in what is now Texas and Oklahoma. The large number of specimens found make it the best-known caseid. Like all large herbivorous caseids, Cotylorhynchus had a short snout sloping forward and very large external nares. The head was very small compared to the size of the body. The latter was massive, barrel-shaped, and ended with a long tail. The limbs were short and robust. The hands and feet had short, broad fingers with powerful claws. The barrel-shaped body must have housed large intestines, suggesting that the animal had to feed on a large quantity of plants of low nutritional value. Caseids are generally considered to be terrestrial, though a semi-aquatic lifestyle has been proposed by some authors. The genus Cotylorhynchus is represented by three species, the largest of which could reach more than 6 m in length. However, a study published in 2022 suggests that the genus may be paraphyletic, with two of the three species possibly belonging to separate genera.
Nigerpeton is an extinct genus of crocodile-like temnospondyls from the late Permian (Changhsingian) period. These temnospondyls lived in modern-day Niger, which was once part of central Pangaea, about 250 million years ago. Nigerpeton is a member of the Cochleosauridae family, a group of edopoid temnospondyl amphibians known from the late Carboniferous (Pennsylvanian) and early Permian (Cisuralian).
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.
Acherontiscus is an extinct genus of stegocephalians that lived in the Early Carboniferous of Scotland. The type and only species is Acherontiscus caledoniae, named by paleontologist Robert Carroll in 1969. Members of this genus have an unusual combination of features which makes their placement within amphibian-grade tetrapods uncertain. They possess multi-bone vertebrae similar to those of embolomeres, but also a skull similar to lepospondyls. The only known specimen of Acherontiscus possessed an elongated body similar to that of a snake or eel. No limbs were preserved, and evidence for their presence in close relatives of Acherontiscus is dubious at best. Phylogenetic analyses created by Marcello Ruta and other paleontologists in the 2000s indicate that Acherontiscus is part of Adelospondyli, closely related to other snake-like animals such as Adelogyrinus and Dolichopareias. Adelospondyls are traditionally placed within the group Lepospondyli due to their fused vertebrae. Some analyses published since 2007 have argued that adelospondyls such as Acherontiscus may not actually be lepospondyls, instead being close relatives or members of the family Colosteidae. This would indicate that they evolved prior to the split between the tetrapod lineage that leads to reptiles (Reptiliomorpha) and the one that leads to modern amphibians (Batrachomorpha). Members of this genus were probably aquatic animals that were able to swim using snake-like movements.
Odonterpeton is an extinct genus of "microsaur" from the Late Carboniferous of Ohio, containing the lone species Odonterpeton triangulare. It is known from a single partial skeleton preserving the skull, forelimbs, and the front part of the torso. The specimen was found in the abandoned Diamond Coal Mine of Linton, Ohio, a fossiliferous coal deposit dated to the late Moscovian stage, about 310 million years ago.
Trihecaton is an extinct genus of microsaur from the Late Pennsylvanian of Colorado. Known from a single species, Trihecaton howardinus, this genus is distinctive compared to other microsaurs due to possessing a number of plesiomorphic ("primitive") features relative to the rest of the group. These include large intercentra, folded enamel, and a large coronoid process of the jaw. Its classification is controversial due to combining a long body with strong limbs, features which typically are not present at the same time in other microsaurs. Due to its distinctiveness, Trihecaton has been given its own monospecific family, Trihecatontidae.
Aerosaurus is an extinct genus within Varanopidae, a family of non-mammalian synapsids. It lived between 252-299 million years ago during the Early Permian in North America. The name comes from Latin aes (aeris) “copper” and Greek sauros “lizard,” for El Cobre Canyon in northern New Mexico, where the type fossil was found and the site of former copper mines. Aerosaurus was a small to medium-bodied carnivorous synapsid characterized by its recurved teeth, triangular lateral temporal fenestra, and extended teeth row. Two species are recognized: A. greenleeorum (1937) and A. wellesi (1981).
Ostodolepidae, also spelled Ostodolepididae, is an extinct family of Early Permian tetrapods. Initially they were considered microsaurs, but later were assigned to the group Recumbirostra. Ostodolepids were relatively large, reaching lengths of up to 2 feet (61 cm), terrestrial, and presumably fossorial. Ostodolepid remains have been found from Early Permian beds in Texas, Oklahoma, and Germany.
Recumbirostra is a clade of tetrapods which lived during the Carboniferous and Permian periods. They are thought to have had a fossorial (burrowing) lifestyle and the group includes both short-bodied and long-bodied snake-like forms. At least one species, the long-bodied molgophid Nagini mazonense, lost its forelimbs entirely. Recumbirostra includes the families Pantylidae, Gymnarthridae, Ostodolepidae, Rhynchonkidae and Brachystelechidae, with additional families such as Microbrachidae and Molgophidae being included by some authors. Brachystelechidae and Molgophidae have also been grouped together in the suggested clade Chthonosauria.
Edopoidea is a clade of primitive temnospondyl amphibians including the genus Edops and the family Cochleosauridae. Edopoids are known from the Late Carboniferous and Early Permian of North America and Europe, and the Late Permian of Africa. They are among the most basal temnospondyls, and possess a number of primitive features that were lost in later members of the group.
Proxilodon is an extinct genus of recumbirostran microsaur from the Early Permian Speiser Formation of Kansas, United States. It contains a single species, Proxilodon bonneri,.
Ascendonanus is an extinct genus of varanopid amniote from the Early Permian of Germany. It is one of the earliest specialized arboreal (tree-living) tetrapods currently known and outwardly resembled a small lizard. The animal was about 40 cm long, with strongly curved claws, short limbs, a slender, elongated trunk, and a long tail. It would have preyed on insects and other small arthropods.
Stenokranio is a genus of eryopid temnospondyl from the Permo-Carboniferous Remigiusberg Formation of Germany. It is represented by the type species, Stenokranio boldi, which was named for two specimens collected from the Remigiusberg quarry near Kusel, Saar–Nahe Basin, southwest Germany.