Sauropterygians Temporal range: Early Triassic - Late Cretaceous, | |
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Sauropterygia diversity. Clockwise from top left: Ceresiosaurus calcagnii (Nothosauroidea), Henodus chelyops (Placodontia), Brachauchenius lucasi , Aristonectes parvidens (Plesiosauria). | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Reptilia |
Clade: | Neodiapsida |
Superorder: | † Sauropterygia Owen, 1860 |
Subgroups | |
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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. It is possible that sauropterygians are a distant relatives of turtles, uniting them under the group Pantestudines, although this is still debatable as sauropterygians might be archosauromorphs or completely unrelated to both.
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 age 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 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]
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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]
Crown Reptilia/ | |
Sauria |
In cladistic analysis of 2015, Sauropterygia placed within Pantestudines: [5]
Sauria | |
(=Archelosauria) |
The following cladogram was found by Simões et al. (2022): [4]
Neoreptilia |
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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]
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.
Dinocephalosaurus is a genus of long necked, aquatic protorosaur that inhabited the Triassic seas of China. The genus contains the type and only known species, D. orientalis, which was named by Chun Li in 2003. Unlike other long-necked protorosaurs, Dinocephalosaurus convergently evolved a long neck not through elongation of individual neck vertebrae, but through the addition of neck vertebrae that each had a moderate length. As indicated by phylogenetic analyses, it belonged in a separate lineage that also included at least its closest relative Pectodens, which was named the Dinocephalosauridae in 2021. Like tanystropheids, however, Dinocephalosaurus probably used its long neck to hunt, utilizing the fang-like teeth of its jaws to ensnare prey; proposals that it employed suction feeding have not been universally accepted. It was probably a marine animal by necessity, as suggested by the poorly-ossified and paddle-like limbs which would have prevented it from going ashore.
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.
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.
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.
Parareptilia ("near-reptiles") is an extinct 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.
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.
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.
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).
Paraplacodus broilii is an extinct placodont sauropterygian from the Middle Triassic epoch, from the Anisian until Ladinian stages. The fossils were uncovered in Northern Italy and the species was named in 1931 by Bernhard Peyer. Paraplacodus means "Almost Placodus", in reference to its similarity to Placodus.
Thalattosauria is an extinct order of 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.
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.
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.
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.
Pantestudines or Pan-Testudines is the proposed 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.
Pappochelys is an extinct genus of diapsid reptile possibly related to turtles. The genus contains only one species, Pappochelys rosinae, from the Middle Triassic of Germany, which was named by paleontologists Rainer Schoch and Hans-Dieter Sues in 2015. The discovery of Pappochelys provides strong support for the placement of turtles within Diapsida, a hypothesis that has long been suggested by molecular data, but never previously by the fossil record. It is morphologically intermediate between the definite stem-turtle Odontochelys from the Late Triassic of China and Eunotosaurus, a reptile from the Middle Permian of South Africa.
Saurosphargidae is an extinct family of marine reptiles known from the Early Triassic and early Middle Triassic of Europe and China.
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.