Rhynchonkos

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Rhynchonkos
Temporal range: Early Permian Cisuralian
Rhynchonkos.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Order: Microsauria
Clade: Recumbirostra
Family: Goniorhynchidae
Carroll and Gaskill, 1978
Genus: Rhynchonkos
Schulze and Foreman, 1981
Type species
Rhynchonkos stovalli
(Olson, 1970) (originally Goniorhynchus stovalli)
Synonyms
  • GoniorhynchusOlson, 1970

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; [1] the family, likewise, was originally named Goniorhynchidae but renamed in 1988. [2] The type and only known species is R. stovalli, found from the Early Permian Fairmont Shale in Cleveland County, Oklahoma. [3] [4] 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. [5] However, such a relationship is no longer widely accepted. [6] [7]

Contents

Description

Rhynchonkos has an elongated body with at least 37 presacral vertebrae. Most vertebrae have ribs. Unlike other microsaurs, the atlas of Rhynchonkos lacks ribs. Both Rhynchonkos and Euryodus have atlases that bear a strong resemblance to those of nectrideans. Like nectrideans, the arch of the atlas is attached to the centrum, although this is likely the result of convergence. [8]

The skull is triangular in dorsal view. The limbs are very small. It has a pointed, overhanging snout that extends beyond the tooth row. There are five or six premaxillary teeth and sixteen maxillary teeth, all of which are narrow and peg-shaped. The palate also has teeth, with rows on the ectopterygoid, palatine, and vomer. The bones of the skull roof are similar to those of gymnarthrids. There are two rows of teeth adjacent to one another in the lower jaw, with a marginal row on the dentary and an inner row on the coronoid. [3]

Classification

Rhynchonkos was first described as Goniorhynchus by Olson (1970). [9] However, the name Goniorhynchus was preoccupied by an Indian moth named in 1896. [10] Because of this preoccupation, it was renamed Rhynchonkos by Schultze and Foreman (1981). [1] Rhynchonkos was first described as a gymnarthrid, but was soon placed in its own family, which was at first called Goniorhynchidae. [3] However, Goniorhynchidae was named before Rhynchonkos was given as a replacement name for the genus. Citing what is currently Article 39 of the International Code of Zoological Nomenclature, Zanon (1988) [2] pointed out that if any family is to bear the name Goniorhynchidae, it must be based on the valid genus Goniorhynchus Hampson, 1896, not on the invalid Goniorhynchus Olson, 1970; he therefore coined the replacement name Rhynchonkidae, which has been used in some works. [11] [12]

Relationship to caecilians

Eocaecilia micropodia, an early caecilian that shares many similarities with Rhynchonkos Eocaecilia BW.jpg
Eocaecilia micropodia , an early caecilian that shares many similarities with Rhynchonkos

Rhynchonkos shares many features with the early caecilian Eocaecilia, including an elongated snout, small limbs, and a similar skull. Based on these features, it has been suggested that caecilians originated from Rhynchonkos or another closely related microsaur. [5] Carroll and Currie (1975), the first to suggest this possible relationship, noted similarities in temporal fenestration, palatal structure, braincase composition, and mandibular dentition. [13] In the temporal region of the skulls of Rhynchonkos and caecilians, the number of bones is reduced. Both Rhynchonkos and caecilians possess a primitive combination of palatal bones, including the ectopterygoid. The two taxa also have rows of teeth on the palate in addition to the marginal rows on the maxilla and premaxilla. Carroll and Currie also mentioned that Rhynchonkos and caecilians have a pleurosphenoid that joins the otic-occipital portion of the braincase with the sphenethmoid, a characteristic which they considered unique among amphibians. The adjacent tooth rows on the coronoid and the dentary of Rhynchonkos were also considered a characteristic that linked it with caecilians. [14]

Despite these similarities, many of the characteristics that suggested a close relationship between Rhynchonkos and caecilians have since been considered primitive, convergent, or indeterminate. For example, tooth rows on the palate have evolved multiple times independently in early amphibians. [14] The general appearance of Rhynchonkos is similar to that of caecilians, but is also similar to other amphibians that have independently developed elongated bodies. Adelospondyls, lysorophians, aïstopods, and some salamanders all have an increased number of vertebrae that lengthen the body. Reduced limbs are seen in many aquatic or burrowing amphibians, and are not unique to microsaurs and caecilians. [6]

Related Research Articles

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"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> Polyphyletic group of tetrapodomorphs

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">Reptiliomorpha</span> Clade of reptile-like animals

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<i>Westlothiana</i> Extinct genus of tetrapods

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

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

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<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.

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

Euryodus is an extinct genus of microsaur within the family Gymnarthridae. Euryodus is a Lepospondyl from the clade Microsauria that lived during the Lower Permian. The name comes from Greek, meaning ‘broad-tooth’. It has been found in the southern half of North America, from its original discovery in Texas up to Utah.

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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.

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<span class="mw-page-title-main">Tuditanomorpha</span> Extinct suborder of amphibians

Tuditanomorpha is a suborder of microsaur lepospondyls. Tuditanomorphs lived from the Late Carboniferous to the Early Permian and are known from North America and Europe. Tuditanomorphs have a similar pattern of bones in the skull roof. Tuditanomorphs display considerable variability, especially in body size, proportions, dentition, and presacral vertebral count. Currently there are four families of tuditanomorphs, with two being monotypic. Tuditanids first appear in the Lower Pennsylvanian. Goniorhynchidae, Hapsidopareiidae, and Trihecatontidae appear in the Late Pennsylvanian and Early Permian.

<span class="mw-page-title-main">Gymnarthridae</span> Extinct family of amphibians

Gymnarthridae is an extinct family of the group Recumbirostra. Gymnarthrids are known from Europe and North America and existed from the Late Carboniferous through the Early Permian. Remains have been found from the Czech Republic, Nova Scotia, Illinois, Texas, and Oklahoma. Previously they were considered tuditanomorph microsaurs.

<span class="mw-page-title-main">Tuditanidae</span> Extinct family of tetrapods

Tuditanidae is an extinct family of microsaurian tetrapods. Fossils have been found from Nova Scotia, Ohio, and the Czech Republic and are Late Carboniferous in age.

Altenglanerpeton is an extinct genus of microsaur tetrapod 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 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.

Huskerpeton is an extinct genus of recumbirostran from the Early Permian period. They belong to the order Microsauria, which was established in 1863 by Dawson, and was quickly expanded to include many different small taxa. They lived in what is now Nebraska and Kansas. The holotype of Huskerpeton was uncovered at the Eskridge formation in Nebraska, which is part of how it got its name.

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,.

References

  1. 1 2 Schultze, H.-P.; Foreman, B. (1981). "A new gymnarthrid microsaur from the Lower Permian of Kansas with a review of the tuditanomorph microsaurs (Amphibia)". Occasional Papers of the Museum of Natural History, the University of Kansas. Lawrence. 91: 1–25.
  2. 1 2 Zanon, R. T. (1988). "A replacement name for the family Goniorhynchidae Carroll and Gaskill, 1978 (Amphibia: Microsauria)". Journal of Paleontology . 62 (2): 317. doi:10.1017/S0022336000030031. S2CID   87467293.
  3. 1 2 3 Carroll, R. L.; Gaskill, P. (1978). "The order Microsauria". Memoirs of the American Philosophical Society. 126.
  4. Szostakiwskyj, M.; Pardo, J. D.; Anderson, J. S. (2015). "Micro-CT study of Rhynchonkos stovalli (Lepospondyli, Recumbirostra), with description of two new genera". PLOS ONE. 10 (6): e0127307. Bibcode:2015PLoSO..1027307S. doi: 10.1371/journal.pone.0127307 . PMC   4465623 . PMID   26061187.
  5. 1 2 Carroll, R. L. (2001). "The origin and early radiation of terrestrial vertebrates" (PDF). Journal of Paleontology . 75 (6): 1202–1213. doi:10.1666/0022-3360(2001)075<1202:toaero>2.0.co;2. S2CID   59359868.
  6. 1 2 Jenkins, F. A.; Walsh, D. M.; Carroll, R. L. (2007). "Anatomy of Eocaecilia micropodia, a limbed caecilian of the Early Jurassic" (PDF). Bulletin of the Museum of Comparative Zoology. 158 (6): 285–366. doi:10.3099/0027-4100(2007)158[285:AOEMAL]2.0.CO;2. S2CID   86379456.
  7. Cannatella, D. C.; Vieites, D. R.; Zhang, P.; Wake, M. H.; Wake, D. B. (2009). "Amphibians (Lissamphibia)". In Hedges, S. B.; Kumar, S. (eds.). The Timetree of Life. Oxford University Press. pp. 353–356.
  8. Carroll, R. L.; Chorn, J. (1995). "Vertebral development in the oldest microsaur and the problem of "lepospondyl" relationships". Journal of Vertebrate Paleontology. 15 (1): 37–56. doi:10.1080/02724634.1995.10011206.
  9. Olson, E.C. (1970). "New and little known genera and species of vertebrates from the Lower Permian of Oklahoma". Fieldiana. 18 (3): 359–434.
  10. Hampson, G. F. (1896). The Fauna of British India, Including Ceylon and Burma: Moths Volume IV. Taylor and Francis via Biodiversity Heritage Library.
  11. Laurin, M.; Reisz, R. R. (1997). "A new perspective on tetrapod phylogeny". In Sumida, S.S.; Martin, K.L.M. (eds.). Amniote Origins: Completing the Transition to Land. Academic Press. pp. 9–60. ISBN   9780126764604.
  12. Marjanović, David; Laurin, Michel (2013). "The origin(s) of extant amphibians: a review with emphasis on the "lepospondyl hypothesis". Geodiversitas. 35 (1): 207–272. doi:10.5252/g2013n1a8. S2CID   67823991.
  13. Carroll, R. L.; Currie, P. J. (1975). "Microsaurs as possible apodan ancestors" (PDF). Zoological Journal of the Linnean Society. 57 (3): 229–247. doi:10.1111/j.1096-3642.1975.tb00817.x.
  14. 1 2 Bolt, J.R. (1991). "Lissamphibian origins". In Schultze, H.-P.; Trueb, L. (eds.). Origins of the Higher Groups of Tetrapods: Controversy and Consensus. Cornell University Press. pp. 194–222. ISBN   9780801424977.