Lysorophia

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Lysorophia
Temporal range: Pennsylvanian–Cisuralian
Scientific classification Red Pencil Icon.png
Kingdom: Animalia
Phylum: Chordata
Superclass: Tetrapoda
Clade: Recumbirostra
Order: Lysorophia
Romer, 1930
Family: Molgophidae
Cope, 1875
Genera
Synonyms

Lysorophia is an order of fossorial Carboniferous and Permian tetrapods within the Recumbirostra. Lysorophians resembled small snakes, as their bodies are extremely elongate. There is a single family, the Molgophidae (previously known as Lysorophidae). Currently there are around five genera included within Lysorophia, although many may not be valid. [1]

Contents

Description

The skull of Brachydectes in multiple views Brachydectes skull.PNG
The skull of Brachydectes in multiple views

The skull is heavily built but with large lateral openings to accommodate jaw musculature, with small orbits restricted to the anterior edge of the large fenestrae. The intertemporal, supratemporal, postfrontal, and jugal bones of the skull have disappeared. The mandibles are short and robust with a small number of large triangular teeth. Although it was initially thought that the maxilla and premaxilla were freely movable, detailed anatomical studies show that this is not the case. [2] The braincase is extremely robust, [1] suggesting that lysorophians engaged in headfirst burrowing.

The torso is very elongate, the limbs diminutive or absent, and the tail short. There are up to 99 pre-sacral (i.e. not including the hips and tail) vertebrae.

Based on morphology of the cranio-vertebral articulation and internal structure of the head, lysorophians are usually considered to be related to the Microsauria, although the pattern of bones of the skull is somewhat different. [3]

Distribution

Lysorophia (geographic distribution).pngMazon CreekJarrowToftshaw
    Pennsylvanian (Upper Carboniferous) sites
    Permian sites
    Doubtful lysorophian site
Lysorophia (geographic distribution).pngMazon CreekJarrowToftshaw
Geographic distribution of Lysorophia after Wellstead (1991)

Lysorophians are known mainly from the Pennsylvanian and Early Permian of North America. [4] In North America, fossils of lysorophians have been found from places such as the Cutler Formation in San Juan County, Utah and the Mazon Creek fossil beds in Grundy County, Illinois. Carboniferous lysorophians are also known from Europe, having been found from Britain and Ireland. Possible remains of a lysorophian have also been found from La Machine, France, although they may belong to an aïstopod. [3] [5]

Paleoecology

Swim traces referrable to lysorophians have been found at the Robledo mountains of New Mexico, an area famous for its Permian tetrapod trackways. Designated as the ichnogenus Serpentichnus, these marks occur as a series of L-shaped grooves, which are divided into two shafts: a long, diagonal shaft preceded by a shorter, forward-pointing shaft offset at a 150∘ angle. What seem to be tiny foot impressions occur on either side of the series of groves. When originally described in 2003, Serpentichnus tracks were argued to have been formed by a long-bodied animal with small limbs, moving in a "sidewinding" motion along a riverbed. Lysorophians such as Brachydectes were considered to be the most likely candidates for these swim traces. [6]

However, some paleontologists have argued that Serpentichnus traces were not actually formed by animals. These sources argue that the grooves were "tool marks", meaning that they were formed by rocks or vegetation brushing against the riverbed while being carried by a current. [7]

Related Research Articles

<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">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">Adelospondyli</span> Extinct order of amphibians

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.

<span class="mw-page-title-main">Aistopoda</span> Extinct order of amphibians

Aistopoda is an order of highly specialised snake-like stegocephalians known from the Carboniferous and Early Permian of Europe and North America, ranging from tiny forms only 5 centimetres (2 in), to nearly 1 metre (3.3 ft) in length. They first appear in the fossil record in the Mississippian period and continue through to the Early Permian.

Lethiscus is the earliest known representative of the Aistopoda, a group of very specialised snake-like amphibians known from the early Carboniferous (Mississippian).

<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">Diadectidae</span> Extinct family of tetrapods

Diadectidae is an extinct family of early tetrapods that lived in what is now North America and Europe during the Late Carboniferous and Early Permian in Asia during the Late Permian. They were the first herbivorous tetrapods, and also the first fully terrestrial animals to attain large sizes. Footprints indicate that diadectids walked with an erect posture. They were the first to exploit plant material in terrestrial food chains, making their appearance an important stage in both vertebrate evolution and the development of terrestrial ecosystems.

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

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 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 considered amphibians, many had characteristics, such as scales and armour-like bony plates, that distinguish them from modern amphibians (lissamphibians).

<span class="mw-page-title-main">Nectridea</span> Extinct order of amphibians

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.

<span class="mw-page-title-main">Microsauria</span> Extinct order of amphibians

Microsauria is an extinct, possibly polyphyletic order of tetrapods from the late Carboniferous and early Permian periods. It is the most diverse and species-rich group of lepospondyls. Recently, Microsauria has been considered paraphyletic, as several other non-microsaur lepospondyl groups such as Lysorophia seem to be nested in it. Microsauria is now commonly used as a collective term for the grade of lepospondyls that were originally classified as members of Microsauria.

<i>Limnoscelis</i> Genus of diadectomorphs

Limnoscelis was a genus of large diadectomorph tetrapods from the Late Carboniferous of western North America. It includes two species: the type species Limnoscelis paludis from New Mexico, and Limnoscelis dynatis from Colorado, both of which are thought to have lived concurrently. No specimens of Limnoscelis are known from outside of North America. Limnoscelis was carnivorous, and likely semiaquatic, though it may have spent a significant portion of its life on land. Limnoscelis had a combination of derived amphibian and primitive reptilian features, and its placement relative to Amniota has significant implications regarding the origins of the first amniotes.

<i>Lysorophus</i> Genus of amphibians

Lysorophus is a genus of Lysorophia, extinct Permian Lepospondyl tetrapods. Most of the specimens are found from North America and attributed to the first formally described species Lysorophus tricarinatus due to the lack of diagnostic characters, but several other species have been described. Lysorophus were small salamander-like amphibians. They lived in fresh water, aestivating in burrows during dry periods.

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

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.

Megamolgophis is an extinct genus of eel-like tetrapod, possibly belonging to the group Lysorophia. Fossils from this genus have been found in the Allegheny mountains of the eastern United States. The genus is endemic to geological formations of this area, such as the Greene and Washington formations of the Early Permian Dunkard Group, as well as the Pennsylvanian Conemaugh Group.

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

Rhynchonkos is an extinct genus of microsaur. It is the only known member of the family Rhynchonkidae. 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.

Stegotretus is an extinct genus of lepospondyl microsaur referred to the Pantylidae. It is known from the Carboniferous–Permian boundary Cutler Formation exposures of New Mexico.

Altenglanerpeton is an extinct genus of microsaur amphibian from the Late Carboniferous or Early Permian of Germany. Altenglanerpeton was named in 2012 after the Altenglan Formation in which it was found. The type and only species is A. schroederi.

<span class="mw-page-title-main">Recumbirostra</span> Extinct clade of tetrapods

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 molgophid Nagini mazonense, lost its forelimbs entirely. It includes the families Pantylidae, Gymnarthridae, Ostodolepidae, Rhynchonkidae and Brachystelechidae, with additional families such as Microbrachidae and Molgophidae being included by some authors.

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

Andersonerpeton is an extinct genus of aïstopod from the Bashkirian of Nova Scotia, Canada. It is known from a single jaw, which shares an unusual combination of features from both other aistopods and from stem-tetrapod tetrapodomorph fish. As a result, Andersonerpeton is significant for supporting a new classification scheme which states that aistopods evolved much earlier than previously expected. The genus contains a single species, A. longidentatum, which was previously believed to have been a species of the microsaur Hylerpeton.

References

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  2. Bolt, John R.; Wassersug, Richard J. (1975). "Functional Morphology of the Skull in Lysorophus: A Snake-Like Paleozoic Amphibian (Lepospondyli)". Paleobiology. 1 (3): 320–332. doi:10.1017/s0094837300002566. JSTOR   2400372.
  3. 1 2 Wellstead, C. F. (1991). "Taxonomic revision of the Lysorophia, Permo-Carboniferous lepospondyl amphibians" (PDF). Bulletin of the American Museum of Natural History. 209: 1–90.
  4. Cannatella, D.C.; Vieites D.R.; ZHang P.; Wake M.H.; Wake D.B. (2009). "Amphibians (Lissamphibia)". In Hedges S.B. & Kumar S. (ed.). The Timetree of Life. Oxford University Press. p. 354. ISBN   9780191608988 . Retrieved 3 December 2012.
  5. Baird, D. (1964). "The aïstopod amphibians surveyed". Breviora. 206: 1–17.
  6. Braddy, Simon J.; Morrissey, Lance B.; Yates, Adam M. (24 November 2003). "Amphibian swimming traces from the Lower Permian of southern New Mexico". Palaeontology. 46 (4): 671–683. doi: 10.1111/1475-4983.00315 . ISSN   0031-0239.
  7. Voigt, Sebastian; Lucas, Spencer G. (2015). "Permian tetrapod ichnodiversity of the Prehistoric Trackways National Monument (south-central New Mexico, U.S.A.)". New Mexico Museum of Natural History and Science Bulletin. 65: 153–167.

General references