Sauropterygia

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Sauropterygians
Temporal range: Early Triassic - Late Cretaceous, 247–66  Ma
Sauropterygia.png
Sauropterygia diversity. Clockwise from top left: Ceresiosaurus calcagnii (Nothosauroidea), Henodus chelyops (Placodontia), Brachauchenius lucasi , Aristonectes parvidens (Plesiosauria).
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Clade: Neodiapsida
Superorder: Sauropterygia
Owen, 1860
Subgroups

Sauropterygia ("lizard flippers") is an extinct taxon of diverse, aquatic reptiles that developed from terrestrial ancestors soon after the end-Permian extinction and flourished during the Triassic before all except for the Plesiosauria became extinct at the end of that period. The plesiosaurs would continue to diversify until the end of the Mesozoic. Sauropterygians are united by a radical adaptation of their pectoral girdle, adapted to support powerful flipper strokes. Some later sauropterygians, such as the pliosaurs, developed a similar mechanism in their pelvis.

Contents

Origins and evolution

Kronosaurus and Woolungasaurus, the plesiosaurs Kronosaurus hunt1DB.jpg
Kronosaurus and Woolungasaurus , the plesiosaurs

The earliest sauropterygians appeared about 247 million years ago (Ma), at the start of the Middle Triassic: the first definite sauropterygian with exact stratigraphic datum lies within the Spathian division of the Olenekian era in South China. [1] Early examples were small (around 60 cm), semi-aquatic lizard-like animals with long limbs (pachypleurosaurs), but they quickly grew to be several metres long and spread into shallow waters (nothosaurs). The Triassic-Jurassic extinction event wiped them all out except for the plesiosaurs. During the Early Jurassic, these diversified quickly into both long-necked small-headed plesiosaurs proper, and short-necked large-headed pliosaurs. Originally, it was thought that plesiosaurs and pliosaurs were two distinct superfamilies that followed separate evolutionary paths. It now seems that these were simply morphotypes in that both types evolved a number of times, with some pliosaurs evolving from plesiosaur ancestors, and vice versa.

Classification

Classification of sauropterygians has been difficult. The demands of an aquatic environment caused the same features to evolve multiple times among reptiles, an example of convergent evolution. Sauropterygians are diapsids, and since the late 1990s, scientists have suggested that they may be closely related to turtles. The bulky-bodied, mollusc-eating placodonts may also be sauropterygians, or intermediate between the classic eosauropterygians and turtles. Several analyses of sauropterygian relationships since the beginning of the 2010s have suggested that they are more closely related to archosaurs (birds and crocodilians) than to lepidosaurs (lizards and snakes). [2] Some authors have suggested that Sauropterygians form a clade with two other groups of marine reptiles, Ichthyosauromorpha and Thalattosauria, with this clade either being placed as non-saurian diapsids or as basal archosauromorphs. [3] [4]

The cladogram shown hereafter is the result of an analysis of sauropterygian relationships (using just fossil evidence) conducted by Neenan and colleagues, in 2013. [3]

The cladogram shown below follows the most likely result found by an analysis of turtle relationships using both fossil and genetic evidence by M.S. Lee, in 2013. This analysis resolved Sauropterygia as a paraphyletic assemblage of stem turtles. [2]

In cladistic analysis of 2015, Sauropterygia placed within Pantestudines: [5]

The following cladogram was found by Simões et al. (2022): [4]

Ecology

Placodonts are thought to have been durophagous, using rounded teeth to crush hard shelled organisms. [6] Members of Eosauropterygia are thought to have been piscivores and carnivores. [7]

Related Research Articles

Several groups of tetrapods have undergone secondary aquatic adaptation, an evolutionary transition from being purely terrestrial to living at least part of the time in water. These animals are called "secondarily aquatic" because although their ancestors lived on land for hundreds of millions of years, they all originally descended from aquatic animals. These ancestral tetrapods had never left the water, and were thus primarily aquatic, like modern fishes. Secondary aquatic adaptations tend to develop in early speciation as the animal ventures into water in order to find available food. As successive generations spend more time in the water, natural selection causes the acquisition of more adaptations. Animals of later generations may spend most their life in the water, coming ashore for mating. Finally, fully adapted animals may take to mating and birthing in water or ice.

<span class="mw-page-title-main">Archosauromorpha</span> Infraclass of reptiles

Archosauromorpha is a clade of diapsid reptiles containing all reptiles more closely related to archosaurs rather than lepidosaurs. Archosauromorphs first appeared during the late Middle Permian or Late Permian, though they became much more common and diverse during the Triassic period.

<span class="mw-page-title-main">Neodiapsida</span> Clade of reptiles

Neodiapsida is a clade, or major branch, of the reptilian family tree, typically defined as including all diapsids apart from some early primitive types known as the araeoscelidians. Modern reptiles and birds belong to the neodiapsid subclade Sauria.

<i>Nothosaurus</i> Extinct genus of reptiles

Nothosaurus is an extinct genus of sauropterygian reptile from the Triassic period, approximately 240–210 million years ago, with fossils being distributed from North Africa and Europe to China. It is the best known member of the nothosaur order.

<span class="mw-page-title-main">Placodontia</span> Extinct order of Triassic marine reptiles

Placodonts are an extinct order of marine reptiles that lived during the Triassic period, becoming extinct at the end of the period. They were part of Sauropterygia, the group that includes plesiosaurs. Placodonts were generally between 1 and 2 m in length, with some of the largest measuring 3 m (9.8 ft) long.

<span class="mw-page-title-main">Euryapsida</span>

Euryapsida is a polyphyletic group of sauropsids that are distinguished by a single temporal fenestra, an opening behind the orbit, under which the post-orbital and squamosal bones articulate. They are different from Synapsida, which also have a single opening behind the orbit, by the placement of the fenestra. In synapsids, this opening is below the articulation of the post-orbital and squamosal bones. It is now commonly believed that euryapsids are in fact diapsids that lost the lower temporal fenestra. Euryapsids are usually considered entirely extinct, although turtles might be part of the sauropterygian clade while other authors disagree. Euryapsida may also be a synonym of Sauropterygia sensu lato.

<span class="mw-page-title-main">Parareptilia</span> Subclass of reptiles

Parareptilia ("near-reptiles") is a subclass or clade of basal sauropsids/reptiles, typically considered the sister taxon to Eureptilia. Parareptiles first arose near the end of the Carboniferous period and achieved their highest diversity during the Permian period. Several ecological innovations were first accomplished by parareptiles among reptiles. These include the first reptiles to return to marine ecosystems (mesosaurs), the first bipedal reptiles, the first reptiles with advanced hearing systems, and the first large herbivorous reptiles. The only parareptiles to survive into the Triassic period were the procolophonoids, a group of small generalists, omnivores, and herbivores. The largest family of procolophonoids, the procolophonids, rediversified in the Triassic, but subsequently declined and became extinct by the end of the period.

<i>Ceresiosaurus</i> Extinct genus of reptiles

Ceresiosaurus is an extinct aquatic genus of lariosaurine nothosaurid sauropterygian known from the Middle Triassic of Monte San Giorgio, southern Switzerland and northern Italy. Ceresiosaurus, meaning "Lizard of Ceresio". The type species, Ceresiosaurus calcagnii, was named by Bernhard Peyer in 1931. C. calcagnii is known from both the Cava superiore and Cava inferiore beds of the Lower Meride Limestone at Monte San Giorgio, dating to the latest Anisian of the Middle Triassic. Rieppel (1998) suggested that the back then monospecific genus Ceresiosaurus, is a junior synonym of the better known Lariosaurus, yet he kept it type species as a separate species under the new combination L. calcagnii. In 2004, however, this synonymy was objected by Hänni who described and name a second species of Ceresiosaurus, C. lanzi - a separation supported by several other authors since. This species is known only from the stratigraphically younger Cassima beds of Monte San Giorgio, although also from the Lower Meride Limestone, dating to possibly the lowest Ladinian age. The species in a subtropical lagoonal environment with varying open marine influences, and alongside many related but smaller species of nothosaurids and pachypleurosaurids. Ceresiosaurus represents one of the largest vertebrate of up to 3 m (9.8 ft) snout-tail length from the very diversified paleoenvironment of the Middle Triassic Monte San Giorgio.

<i>Pistosaurus</i> Extinct genus of reptiles

Pistosaurus is an extinct genus of aquatic sauropterygian reptile closely related to plesiosaurs. Fossils have been found in France and Germany, and date to the Middle Triassic. It contains a single species, Pistosaurus longaevus. Pistosaurus is known as the oldest "subaquatic flying" reptile on earth.

<i>Cyamodus</i> Extinct genus of reptiles

Cyamodus is a genus of placodonts known from several species described from Middle-Late Triassic of Europe and China. The genus was described by Christian Erich Hermann von Meyer in 1863, based on specimens found in Germany. Like some other placodonts, Cyamodus has an armoured carapace composed of irregular hexagonal plates, with the mouth containing a small number of large, rounded teeth that were likely involved in crushing hard shelled organisms (durophagy).

<span class="mw-page-title-main">Thalattosauria</span> Extinct order of sea reptiles

Thalattosauria is an extinct order of prehistoric marine reptiles that lived in the Middle to Late Triassic. Thalattosaurs were diverse in size and shape, and are divided into two superfamilies: Askeptosauroidea and Thalattosauroidea. Askeptosauroids were endemic to the Tethys Ocean, their fossils have been found in Europe and China, and they were likely semiaquatic fish eaters with straight snouts and decent terrestrial abilities. Thalattosauroids were more specialized for aquatic life and most had unusual downturned snouts and crushing dentition. Thalattosauroids lived along the coasts of both Panthalassa and the Tethys Ocean, and were most diverse in China and western North America. The largest species of thalattosaurs grew to over 4 meters (13 feet) in length, including a long, flattened tail utilized in underwater propulsion. Although thalattosaurs bore a superficial resemblance to lizards, their exact relationships are unresolved. They are widely accepted as diapsids, but experts have variously placed them on the reptile family tree among Lepidosauromorpha, Archosauromorpha, ichthyosaurs, and/or other marine reptiles.

<i>Helveticosaurus</i> Extinct genus of reptiles

Helveticosaurus is an extinct genus of diapsid marine reptile known from the Middle Triassic of southern Switzerland. It contains a single species, Helveticosaurus zollingeri, known from the nearly complete holotype T 4352 collected at Cava Tre Fontane of Monte San Giorgio, an area well known for its rich record of marine life during the Middle Triassic.

Hanosaurus is an extinct genus of marine reptiles that existed during the Triassic period in what is now China. The type species is Hanosaurus hupehensis. It was a small animal, with specimens measuring 79.4 cm (31.3 in) long in total body length, which likely fed on soft-bodied prey.

<i>Palatodonta</i> Extinct genus of reptiles

Palatodonta is an extinct genus of neodiapsid reptile known from the early Middle Triassic of the Netherlands. It was initially described in 2013 as a basal placodontiform closely related to a group of marine reptiles called placodonts, characterized by their crushing teeth and shell-like body armor. Under this interpretation, Palatodonta is transitional between placodonts and less specialized reptiles. Like placodonts, it has a row of large teeth on its palate, but while these teeth are thick and blunt in placodonts, Palatodonta has palatal teeth that are thin and pointed. A 2023 study instead classified it as a sauropterygomorph and the sister taxon to Eusaurosphargis. In other words, it is close to, but not within, Sauropterygia.

<span class="mw-page-title-main">Placodontiformes</span> Extinct clade of reptiles

Placodontiformes is an extinct clade of sauropterygian marine reptiles that includes placodonts and the non-placodont Palatodonta. It was erected in 2013 with the description of Palatodonta. Placodontiformes is the most basal clade of Sauropterygia and the sister group of Eosauropterygia, which includes all other sauropterygians.

<span class="mw-page-title-main">Pantestudines</span> Clade of reptiles

Pantestudines or Pan-Testudines is the group of all reptiles more closely related to turtles than to any other living animal. It includes both modern turtles and all of their extinct relatives. Pantestudines with a complete shell are placed in the clade Testudinata.

<span class="mw-page-title-main">Saurosphargidae</span> Extinct family of reptiles

Saurosphargidae is an extinct family of marine reptiles known from the Early Triassic and early Middle Triassic of Europe and China.

<i>Eusaurosphargis</i> Extinct genus of reptiles

Eusaurosphargis is an extinct genus of a diapsid reptile, known from the Middle Triassic Besano Formation of northern Italy and Prosanto Formation of south-eastern Switzerland. It contains a single species, Eusaurosphargis dalsassoi. It was a small reptile, measuring 20 cm (7.9 in) long.

Paleontology or palaeontology is the study of prehistoric life forms on Earth through the examination of plant and animal fossils. This includes the study of body fossils, tracks (ichnites), burrows, cast-off parts, fossilised feces (coprolites), palynomorphs and chemical residues. Because humans have encountered fossils for millennia, paleontology has a long history both before and after becoming formalized as a science. This article records significant discoveries and events related to paleontology that occurred or were published in the year 2017.

Protenodontosaurus is an extinct genus of placodont from Italy.

References

  1. Ji Cheng, et al. 2013. "Highly diversified Chaohu fauna (Olenekian, Early Triassic) and sequence of Triassic marine reptile faunas from South China", in Reitner, Joachim et al., eds. Palaeobiology and Geobiology of Fossil Lagerstätten through Earth History p. 80
  2. 1 2 Lee, M. S. Y. (2013). "Turtle origins: Insights from phylogenetic retrofitting and molecular scaffolds". Journal of Evolutionary Biology. 26 (12): 2729–2738. doi: 10.1111/jeb.12268 . PMID   24256520. S2CID   2106400.
  3. 1 2 Neenan, J. M.; Klein, N.; Scheyer, T. M. (2013). "European origin of placodont marine reptiles and the evolution of crushing dentition in Placodontia". Nature Communications. 4: 1621. Bibcode:2013NatCo...4.1621N. doi: 10.1038/ncomms2633 . PMID   23535642.
  4. 1 2 Simões, T. R.; Kammerer, C. F.; Caldwell, M. W.; Pierce, S. E. (2022). "Successive climate crises in the deep past drove the early evolution and radiation of reptiles". Science Advances. 8 (33): eabq1898. Bibcode:2022SciA....8.1898S. doi: 10.1126/sciadv.abq1898 . PMC   9390993 . PMID   35984885.
  5. Schoch, Rainer R.; Sues, Hans-Dieter (24 June 2015). "A Middle Triassic stem-turtle and the evolution of the turtle body plan". Nature . 523 (7562): 584–587. Bibcode:2015Natur.523..584S. doi:10.1038/nature14472. PMID   26106865. S2CID   205243837.
  6. Neenan, James M.; Li, Chun; Rieppel, Olivier; Bernardini, Federico; Tuniz, Claudio; Muscio, Giuseppe; Scheyer, Torsten M. (May 2014). "Unique method of tooth replacement in durophagous placodont marine reptiles, with new data on the dentition of Chinese taxa". Journal of Anatomy. 224 (5): 603–613. doi:10.1111/joa.12162. ISSN   0021-8782. PMC   3981503 . PMID   24517163.
  7. Rieppel, Olivier (May 2002). "Feeding mechanics in Triassic stem-group sauropterygians: the anatomy of a successful invasion of Mesozoic seas". Zoological Journal of the Linnean Society. 135 (1): 33–63. doi:10.1046/j.1096-3642.2002.00019.x. ISSN   1096-3642.