This article's factual accuracy is disputed .(October 2022) |
Cyamodus | |
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Fossil skeleton | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Reptilia |
Superorder: | † Sauropterygia |
Order: | † Placodontia |
Superfamily: | † Cyamodontoidea |
Family: | † Cyamodontidae |
Genus: | † Cyamodus Meyer, 1863 |
Species | |
Synonyms | |
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Cyamodus (pron.: SIE-ah-MO-dus) 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).
Thus far, six species of Cyamodus have been identified - C. rostratus, C. munsteri, C. tarnowitzensis, C. hildegardis, C. kuhnschneyderi, [2] and C. orientalis.
Initially considered to be an ancestral turtle due to its testudine-like head and large, bifurcated carapace. However further investigation resulted in its reclassification as a placodont, and it is closely related to other turtle-like reptiles of the Triassic period such as Henodus and Psephoderma . [3] Similar to these other placodonts, Cyamodus lived hovering close to the sea floor, vacuuming up various shellfish, and crushing them between its blunt teeth. [4]
Historically, the first Cyamodus remains were found in Upper Muschelkalk shallow marine limestones at near Bayreuth in Bavaria (Germany). They included the incomplete holotype skulls of Cyamodus muensteri and Cyamodus rostatus, which along with all other placodont remains recovered from the six quarries on the Lainecker Range in northern Bavaria were originally considered to have been derived from fish. [5] The earliest Cyamodus skull was later restored by Muenster, with the addition of four teeth that had not been present in the original skull, and was named Placodus muensteri. [6]
Further placodont remains were found by Muenster, who collected many placodont cranial remains in the Bindlach and Lainecker Range quarries. All placodont remains from those sites were then revised as being of reptilian origin by Owen (1858). A complete Cyamodus skeleton, including its skull, is known for C. hildegardis, which was found outside the Germanic Basin in the northern Tethys in Switzerland. Middle Triassic sauropterygian placodonts have become increasingly important for developing new ideas to the evolutionary history of their relatives, the turtles, whereas modern analyses place placodonts not as their ancestors using morphological cladistic analyses based on the bone osteology. The study of these placodonts contributes to our understanding of the Germanic Basin and the reptile distributions. [6]
An intriguing placodont that appears to be intermediate between Cyamodus and the placochelyids, Protenodontosaurus italicus , was described by Giovanni Pinna in 1990. [4]
Cyamodus was a relatively small reptile, with most species measuring 1.3–1.5 m (4.3–4.9 ft) long and weighing 20–25 kg (44–55 lb); the smallest species, C. rostratus, was about 0.9 m (3.0 ft) long and weighed 5 kg (11 lb). [1] [7] [8] [9] It was a heavily armored swimmer that fed mainly on shellfish that it was specialized to uproot and crush with its powerful jaws. [3] The body of Cyamodus, specifically the armor, has been described as possessing a turtle-like flatness. The shell was a two-part carapace on the upper surface of the body. The larger half covered Cyamodus from the neck to the hips and spread out flat, almost encompassing the limbs. The second, smaller plate covered the hips and the base of the tail. The shells themselves are covered in hexagonal or circular plates of armor. The skull is heart-shaped and broad. [2]
Distinct from Paraplacodus, the skull of Cyamodus had a shorter rostrum, a smaller orbit and a larger upper temporal fenestra that was rimmed by ossifications. The teeth were flat discs, only one tooth appeared on each premaxilla and only two teeth appeared on each maxilla, with the largest teeth on the pterygoid. The quadratojugal joined the squamosal and sealed up the lateral temporal fenestra from the ancestral species (Paraplacodus). [10]
The carapace of C. hildegardis has a series of similar-sized, enlarged lateral armor plates is rounder and less laterally expanded than was hypothesized. The separate pelvic shield, also carrying a smaller set of lateral armor plates that decrease in size with an anterior/posterior gradient covering mainly the pelvic girdle and the base of the tail. The short tail is armored by four series of armor plates that also show an anterior/posterior gradient of size reduction equivalent to the size reduction of the caudal vertebrae. [11] Until further fossils are recovered, the internal organisation of dermal plates within the two armor shields of C. hildegardis remains little known. [6]
Cyamodus did not have any dorsal spines, although it did have a wing-like elongated flattened lateral spine that served to brace the overlying subdermal carapace. Presumably, the dorsal spines disappeared to provide a closer and better braced association between the vertebrae and the carapace. [6]
Although the shell would most likely have been too cumbersome for highly adept swimming, Cyamodus would still have been more agile than other single shelled placodonts like Henodus. [12] The shells were also covered in hexagonal plates that not only increased the level of protection but also increased their weight, a typical placodont adaptation as additional weight just beyond the level of neutral buoyancy allowed them to dive to reach shellfish. Other adaptations for protection besides the heavily armored shell include the strongly built rear of the skull and limbs that do not protrude too far. Although the reduction in limb length restricted its ability to swim, its heavy shell greatly assisted its ability to dive. Cyamodus is also expected to have had difficulty maneuvering on land and probably only ventured out of the water for periods of rest. Discovery of two fossil Cyamodus juveniles inside the stomach area of a Lariosaurus fossil has led to speculation about its vulnerability to predation. [13] [14]
It has also been noted that juvenile specimens of Cyamodus have an extra tooth on the roof of their mouth, compared to adult specimens. This suggests that Cyamodus reduced the number of teeth as they grew to maturity. However, this could be due to a difference between species of Cyamodus. [4]
C. hildegardis from the Besano Formation (Middle Triassic) of the Alpine area of Switzerland and northern Italy has been reconstructed with a broad, laterally expanded main armor (carapace) and a separate smaller pelvic shield, giving it a sprawling appearance. [11] A reexamination of the postcranial dermal armor and endoskeletal elements of the three best preserved articulated specimens of the species has led to new interpretations of the dermal armor and underlying postcranial bones, as well as a new life reconstruction. [6] [11]
Placodonts are typically considered to be durophagous (adapted to crushing hard-shelled organisms). [15] C.G. Diedrich has suggested that Cyamodus and other placodonts were algae-grazers. [6] However, this interpretation has been criticized by Torsten M. Scheyer and other researchers, [15] and many subsequent studies about placodonts have rejected Deidrich's interpretation, and the consensus that placodonts with the exception of Henodus were durophagous still continues to be strongly supported. [16] [17] [18] [19] [20] [21]
Sauropterygia 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.
Placodus is an extinct genus of marine reptiles belonging to the order Placodontia, which swam in the shallow seas of the middle Triassic period. Fossils of Placodus have been found in Central Europe and China.
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.
Placochelys is an extinct genus of placodont reptiles erected by Otto Jaekel in 1902.
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.
Omphalosaurus is an extinct genus of marine reptile from the Early Triassic to Middle Triassic, thought to be in the order of Ichthyosauria. Most of what is known about Omphalosaurus is based on multiple jaw fragments, ribs, and vertebrae. Specimens of Omphalosaurus have been described from the western United States, Poland, Austria and the island of Spitsbergen off the northern coast of Norway.
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.
Wimanius is a genus of ichthyosaur from the Middle Triassic of Switzerland, containing a single species, Wimanius odontopalatus. It was described by Michael Maisch and Andreas Matzke in 1998 based on an incomplete skull from Monte San Giorgio, a mountain on the Swiss-Italian border. Wimanius possesses teeth on its palate, though whether they were located on the palatine or pterygoid is disputed. Other features of Wimanius include a large orbit and jugals with two rami of similar lengths. Different phylogenetic placements of Wimanius have been recovered by different studies, including it being a mixosaurid relative or a merriamosaur, and a monotypic family, Wimaniidae has been named for it. However, its validity has also been questioned, and synonymy with various other genera has been proposed. The only specimen of Wimanius come from the Besano Formation. During the Anisian, this region was a lagoon populated by a wide variety of marine life, including a variety of other ichthyosaurs.
Henodus is an extinct placodont of the Late Triassic period during the early Carnian age. Fossils of Henodus chelyops were found in the Estherienschichten Member of the Grabfeld Formation, near Tübingen, Germany. It was around 1 metre (3.3 ft) in length. The single species within the genus is H. chelyops.
Cyamodontoidea is an extinct superfamily of placodont marine reptiles from the Triassic period. It is one of the two main groups of placodonts, the other being Placodontoidea. Cyamodontoids are distinguished from placodontoids by their large shells, formed from fused bony plates called osteoderms and superficially resembling the shells of turtles. Cyamodontoids also have distinctive skulls with narrow, often toothless jaws and wide, flaring temporal regions behind the eyes. Two large temporal openings are positioned at the top of the back of the skull, an arrangement that is known as the euryapsid condition and seen throughout Sauropterygia, the marine reptile group to which placodonts belong. Cyamodontoids are also distinguished by their large crushing teeth, which grow from the palatine bones on the roof of the mouth.
Psephosauriscus is an extinct genus of placodont reptile from the Middle Triassic of Israel and Egypt. It is known from bony armor plates that have been found from Makhtesh Ramon in Israel's Negev desert and Araif en Naqua on Egypt's Sinai Peninsula. The genus was erected in 2002 as a replacement name for several species of the genus Psephosaurus, which was named in 1957. It includes the species P. mosis, P. ramonensis, P. sinaiticus, and a possible fourth species, P. rhombifer. All species, with the exception of P. ramonensis, were once assigned to the genus Psephosaurus. Remains of P. mosis and P. ramonensis were found in Makhtesh Ramon, while P. sinaiticus and P. rhombifer were found in Araif en Naqua.
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.
Macroplacus is an extinct genus of placodont reptiles. The type species is M. raeticus and the fossil record of this species dates back to the upper Triassic, Rhaetian age. These fossils have been found in Germany, at Hinterstein near Hindelang im Allgäu.
The Erfurt Formation, also known as the Lower Keuper, is a stratigraphic formation of the Keuper group and the Germanic Trias supergroup. It was deposited during the Ladinian stage of the Triassic period. It lies above the Upper Muschelkalk and below the Middle Keuper.
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.
Chinlechelys is an extinct genus of stem-turtle belonging to Testudinata. It lived in the Norian age of the Late Triassic and is the oldest turtle known from North America. Among turtles it is unique, mostly because of its very thin shell. The type and only species, C. tenertesta, was named and described with the genus by Walter G. Joyce et al. in 2009. It was probably terrestrial, and was found by Joyce et al. to be closely related to Proganochelys, another terrestrial testudinatan.
Silvestrosaurus is an extinct aquatic genus of lariosaurine nothosaurid sauropterygian known from the Middle Triassic of Monte San Giorgio, southern Switzerland. It contains a single species, Silvestrosaurus buzzii, originally considered to be a species of the closely related Lariosaurus. The species was named by Tschanz in 1989, based solely on the holotype PIMUZ T/2804 comprising the skull, the lower jaw, and a dis-articulated partial postcranial skeleton. Cyamodus hildegardis tooth bearing elements were found in the stomach region of the specimen. The holotype was collected at Punkt 902 of Monte San Giorgio, from layer 97 of the Grenzbitumen zone, dating to the Anisian-Ladinian boundary of the Middle Triassic. Kuhn-Schnyner (1990) reassigned the species to its own genus, creating the combination S. buzzii. The generic name honors a church near the collection locality of the holotype, dedicated to Saint Sylvester, a Pope during the reign of Constantine the Great, and from Greek saurus, meaning "lizard", a common suffix for genus names of extinct reptile.
Protenodontosaurus is an extinct genus of placodont from Italy.