Gerobatrachus

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Gerobatrachus
Temporal range: Early Permian, 290  Ma
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Gerobatrachus NT.jpg
Restoration
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Amphibia
Order: Temnospondyli
Clade: Amphibamiformes
Genus: Gerobatrachus
Anderson et al., 2008
Type species
Gerobatrachus hottoni
Anderson et al., 2008

Gerobatrachus is an extinct genus of amphibamid temnospondyl (represented by the type species Gerobatrachus hottoni) 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.

Contents

Description

The only known specimen of Gerobatrachus is a nearly complete skeleton (USNM 489135) about 11 centimetres (4.3 in) long, that is articulated, preserved in ventral view, missing only the stylopodia, zeugopodia, and ventral portions of the skull and pectoral girdle. It is preserved in red siltstone with only its underside exposed. Like other amphibolid temnospondyls, Gerobatrachus has a rounded and flattened head, well-developed limbs, and a small tail. Its vertebral column is somewhat shorter than those of related amphibolids. The large, round head and shortened vertebral column are features Gerobatrachus shares in common with frogs and the early salamander Karaurus . [1] [2] Gerobatrachus also has a large embayment at the back of the skull called an optic notch, which is seen other amphibolids and in frogs and supports the tympanum, an eardrum-like structure used in hearing. [2]

Many finer details of the skull link Gerobatrachus with modern amphibians. Gerobatrachus has a row of very small pedicellate teeth, a feature shared with modern amphibians. Pedicellate teeth are characterized by two layers of hardened dentine, one at the tooth base and one at the tooth tip, surrounding a middle layer of softer, uncalcified dentine. The palate, which in other amphibians bears many distinguishing characteristics, is poorly preserved in Gerobatrachus. The preserved portion lacks the large palatal teeth commonly found in other temnospondyls. The vomer bone is much shorter in length than it is in other amphibamids, but similar in proportion to living amphibians. As in most frogs, the palatine bone forms a narrow strip along the side of the palate. Gerobatrachus possesses another modern amphibian characteristic at the back of the skull, a widened bone called the parasphenoid basal plate. Many of the features that link Gerobatrachus with modern amphibians are also seen in other amphibamids. For example, the amphibamids Amphibamus , Doleserpeton , Eoscopus , and Platyrhinops also have large otic notches; Amphibamus, Doleserpeton, and Tersomius also have pedicellate teeth; and Amphibamus and Doleserpeton also have a wide parasphenoid plate. [2]

Discovery

Gerobatrachus hottoni was described for the first time on May 22, 2008 in the journal Nature. [2] The nearly complete holotype skeleton USNM 489135 was collected from a fossil locality known as Don's Dump Fish Quarry in Baylor County, Texas in 1995. It was then rediscovered in the collections of the National Museum of Natural History, Washington, D.C., in 2004. The genus name means "elder frog" in Greek, from γέρος (géros, "elder") and βάτραχος (batrakhos, "frog"). The species name honors Nicholas Hotton III, a paleontologist who had worked for the National Museum of Natural History. [2]

Relationships

When Gerobatrachus was first described in 2008, it was incorporated into a phylogenetic analysis that found it to be the sister taxon or closest relative of Batrachia, an evolutionary group that includes living frogs and salamanders but not caecilians, which are the third major lineage of modern amphibians (the three main groups of modern amphibians are collectively known as lissamphibians). As was the case in some previous analyses, caecilians were found to be the descendants of a group of small amphibious Paleozoic tetrapods called Lepospondyli while frogs and salamanders had an independent origin within Temnospondyli. The phylogeny supported by the 2008 analysis has been called the "polyphyletic hypothesis" and is one of three main hypotheses for lissamphibian origins. The other two hypotheses are the "lepospondyl hypothesis", which places all lissamphibians as the closest relatives of a group of lepospondyls called lysorophians, and the "temnospondyl hypothesis", which has all lissamphibians derived from amphibamid temnospondyls like Gerobatrachus. [3] Paleontologists David Marjanović and Michel Laurin published studies in 2008 and 2009 that supported the lepospondyl hypothesis. Their phylogenetic analyses confirmed that Gerobatrachus was an amphibamid temnospondyl, and since all modern amphibians nested within Lepospondyli, it was positioned far from the ancestry of frogs and salamanders. [4] [5] A 2012 study of the stem-caecilian Eocaecilia found Gerobatrachus to group within Lissamphibia. In this phylogeny, Gerobatrachus is more closely related to frogs and salamanders than it is to caecilians, meaning that Gerobatrachus would have been a descendant of the last common ancestor of modern amphibians. [6]

Below is a cladogram from the original 2008 phylogenetic analysis (left) and a cladogram from the 2012 analysis (right):

Tetrapoda

Acanthostega

Proterogyrinus

Seymouria baylorensis

Limnoscelis

Lepospondyli (including caecilians)

Temnospondyli

Greererpeton

Eryops

Balanerpeton

Dendrerpeton

Tambachia

Ecolsonia

Acheloma

Branchiosauridae

Micromelerpetontidae

Tersomius

Micropholis

Eoscopus

Platyrhinops

Amphibamus

Doleserpeton

Gerobatrachus

Batrachia

Triadobatrachus

Anura (frogs)

Albanerpetontidae

Caudata (salamanders)

Tetrapoda

Acanthostega

Proterogyrinus

Seymouria baylorensis

Limnoscelis

Lepospondyli

Temnospondyli

Greererpeton

Eryops

Balanerpeton

Dendrerpeton

Tambachia

Ecolsonia

Acheloma

Branchiosauridae

Micromelerpetontidae

Tersomius

Micropholis

Eoscopus

Platyrhinops

Amphibamus

Doleserpeton

Lissamphibia

Gerobatrachus

Batrachia

Gymnophiona

Eocaecilia

Apoda (caecilians)

Related Research Articles

<span class="mw-page-title-main">Lissamphibia</span> Subclass of amphibians

The Lissamphibia is a group of tetrapods that includes all modern amphibians. Lissamphibians consist of three living groups: the Salientia, the Caudata, and the Gymnophiona.

<span class="mw-page-title-main">Caecilian</span> Order of amphibians

Caecilians are a group of limbless, vermiform (worm-shaped) or serpentine (snake-shaped) amphibians with small or sometimes nonexistent eyes. They mostly live hidden in soil or in streambeds, and this cryptic lifestyle renders caecilians among the least familiar amphibians. Modern caecilians live in the tropics of South and Central America, Africa, and southern Asia. Caecilians feed on small subterranean creatures such as earthworms. The body is cylindrical and often darkly coloured, and the skull is bullet-shaped and strongly built. Caecilian heads have several unique adaptations, including fused cranial and jaw bones, a two-part system of jaw muscles, and a chemosensory tentacle in front of the eye. The skin is slimy and bears ringlike markings or grooves and may contain scales.

<span class="mw-page-title-main">Batrachia</span> Clade of amphibians

The Batrachia are a clade of amphibians that includes frogs and salamanders, but not caecilians nor the extinct allocaudates. The name Batrachia was first used by French zoologist Pierre André Latreille in 1800 to refer to frogs, but has more recently been defined in a phylogenetic sense as a node-based taxon that includes the last common ancestor of frogs and salamanders and all of its descendants. The idea that frogs and salamanders are more closely related to each other than either is to caecilians is strongly supported by morphological and molecular evidence; they are, for instance, the only vertebrates able to raise and lower their eyes. However, an alternative hypothesis exists in which salamanders and caecilians are each other's closest relatives as part of a clade called the Procera, with frogs positioned as the sister taxon of this group.

<span class="mw-page-title-main">Labyrinthodontia</span> Subclass of early amphibious tetrapods

"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.

<span class="mw-page-title-main">Batrachomorpha</span> Clade of amphibians

The Batrachomorpha are a clade containing recent and extinct amphibians that are more closely related to modern amphibians than they are to mammals and reptiles. According to many analyses they include the extinct Temnospondyli; some show that they include the Lepospondyli instead. The name traditionally indicated a more limited group.

<span class="mw-page-title-main">Lepospondyli</span> Extinct subclass of amphibians

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 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. It has been suggested that the grouping is polyphyletic, with aïstopods being primitive stem-tetrapods, while recumbirostran microsaurs are primitive reptiles.

<span class="mw-page-title-main">Reptiliomorpha</span> Clade of reptile-like animals

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.

<span class="mw-page-title-main">Dissorophoidea</span> Extinct superfamily of amphibians

Dissorophoidea is a clade of medium-sized, temnospondyl amphibians that appeared during the Moscovian in Euramerica, and continued through to the Late Permian and the Early Triassic of Gondwana. They are distinguished by various details of the skull, and many species seem to have been well adapted for life on land.

<span class="mw-page-title-main">Temnospondyli</span> Ancestors of modern amphibians adapted to life on land

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.

<i>Eocaecilia</i> Extinct genus of amphibians

Eocaecilia is an extinct genus of gymnophionan amphibian from the early Jurassic Kayenta Formation of Arizona, United States. One species is described, Eocaecilia micropodia.

<span class="mw-page-title-main">Albanerpetontidae</span> Family of amphibians

The Albanerpetontidae are an extinct family of small amphibians, native to the Northern Hemisphere during the Mesozoic and Cenozoic. The only members of the order Allocaudata, they are thought to be allied with living amphibians belonging to Lissamphibia. Despite a superficially salamander-like bodyform, their anatomy is strongly divergent from modern amphibians in numerous aspects. The fossil record of albanerpetontids spans over 160 million years from the Middle Jurassic to the beginning of the Pleistocene, about 2.13–2 million years ago.

Doleserpeton is an extinct, monospecific genus of dissorophoidean temnospondyl within the family Amphibamidae that lived during the Upper Permian, 285 million years ago. Doleserpeton is represented by a single species, Doleserpeton annectens, which was first described by John R. Bolt in 1969. Fossil evidence of Doleserpeton was recovered from the Dolese Brothers Limestone Quarry in Fort Sill, Oklahoma. The genus name Doleserpeton is derived from the initial discovery site in Dolese quarry of Oklahoma and the Greek root "herp-", 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.

<i>Rhynchonkos</i> Extinct genus of amphibians

Rhynchonkos is an extinct genus of rhynchonkid microsaur. Originally known as Goniorhynchus, it was renamed in 1981 because the name had already been given to another genus; the family, likewise, was originally named Goniorhynchidae but renamed in 1988. The type and only known species is R. stovalli, found from the Early Permian Fairmont Shale in Cleveland County, Oklahoma. Rhynchonkos shares many similarities with Eocaecilia, an early caecilian from the Early Jurassic of Arizona. Similarities between Rhynchonkos and Eocaecilia have been taken as evidence that caecilians are descendants of microsaurs. However, such a relationship is no longer widely accepted.

Utaherpeton is an extinct genus of lepospondyl amphibian from the Carboniferous of Utah. It is one of the oldest and possibly one of the most basal ("primitive") known lepospondyls. The genus is monotypic, including only the type species Utaherpeton franklini. Utaherpeton was named in 1991 from the Manning Canyon Shale Formation, which dates to the Mississippian-Pennsylvanian boundary. It was originally classified within Microsauria, a group of superficially lizard- and salamander-like lepospondyls that is now no longer considered to be a valid clade or evolutionary grouping, but rather an evolutionary grade consisting of the most basal lepospondyls. Utaherpeton has been proposed as both the most basal lepospondyl and the oldest "microsaur", although more derived lepospondyls are known from earlier in the Carboniferous. However, its position within Lepospondyli remains uncertain due to the incomplete preservation of the only known specimen. The inclusion of Utaherpeton in various phylogenetic analyses has resulted in multiple phylogenies that are very different from one another, making it a significant taxon in terms of understanding the interrelationships of lepospondyls.

<span class="mw-page-title-main">Salientia</span> Order of amphibians

The Salientia are a total group of amphibians that includes the order Anura, the frogs and toads, and various extinct proto-frogs that are more closely related to the frogs than they are to the Urodela, the salamanders and newts. The oldest fossil "proto-frog" appeared in the early Triassic of Madagascar, but molecular clock dating suggests their origins may extend further back to the Permian, 265 million years ago.

<span class="mw-page-title-main">Amphibamidae</span> Ancient family of amphibians

The Amphibamidae are an ancient family of dissorophoid temnospondyls known from Late Carboniferous-Early Permian strata in the United States.

Pasawioops is an extinct genus of early Permian dissorophoid temnospondyl within the clade Amphibamiformes.

Chinlestegophis is a diminutive Late Triassic stereospondyl that has been interpreted as a putative stem caecilian, a living group of legless burrowing amphibians. If Chinlestegophis is indeed both an advanced stereospondyl and a relative of caecilians, this means that stereospondyls survived to the present day; historically the group was thought to have gone extinct by the early Cretaceous. Chinlestegophis jenkinsi, the type and only species, is known from two partial skulls discovered in the Chinle Formation in Colorado.

<span class="mw-page-title-main">Amphibamiformes</span> Extinct clade of amphibians

Amphibamiformes is an unranked clade with Dissorophoidea created by Schoch (2018). It encompasses all of the taxa traditionally considered to be "amphibamids", branchiosaurids, and hypothetically lissamphibians under the traditional temnospondyl hypothesis of lissamphibian origins. These taxa are typically small-bodied dissorophoids and form the sister group to Olsoniformes, which comprises dissorophids and trematopids.

<i>Funcusvermis</i> Extinct genus of amphibians

Funcusvermis is an extinct genus of stem-caecilian from the Late Triassic of Arizona. It is based on a large sample of jaws and other skull and postcranial fragments, discovered in an approximately 220 million years old layer of rock in the Blue Mesa Member of the Chinle Formation at Petrified Forest National Park. There is a single species, called Funcusvermis gilmorei.

References

  1. Science Daily, "Ancient Amphibian: Debate Over Origin Of Frogs And Salamanders Settled With Discovery Of Missing Link" Accessed 22 May 2008.
  2. 1 2 3 4 5 Anderson, J. S.; Reisz, R. R.; Scott, D.; Frobish, N. B.; Sumida, S. S. (2008). "A stem batrachian from the Early Permian of Texas and the origin of frogs and salamanders". Nature. 453 (7194): 515–518. doi:10.1038/nature06865. PMID   18497824. S2CID   205212809.
  3. Sigurdsen, T.; Green, D. M. (2011). "The origin of modern amphibians: A re-evaluation". Zoological Journal of the Linnean Society. 162 (2): 457. doi: 10.1111/j.1096-3642.2010.00683.x .
  4. David Marjanović and Michel Laurin (2008). "A reevaluation of the evidence supporting an unorthodox hypothesis on the origin of extant amphibians". Contributions to Zoology. 77 (3): 149–199. doi: 10.1163/18759866-07703002 .
  5. David Marjanović and Michel Laurin (2009). "The origin(s) of modern amphibians: a commentary" (PDF). Evolutionary Biology. 36 (3): 336–338. doi:10.1007/s11692-009-9065-8. S2CID   12023942.
  6. Maddin, H. C.; Jenkins, F. A.; Anderson, J. S. (2012). Farke, Andrew A (ed.). "The Braincase of Eocaecilia micropodia (Lissamphibia, Gymnophiona) and the Origin of Caecilians". PLOS ONE. 7 (12): e50743. doi: 10.1371/journal.pone.0050743 . PMC   3515621 . PMID   23227204.