Mystriosuchus Temporal range: Late Triassic | |
---|---|
Skull of M. planirostris | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Reptilia |
Order: | † Phytosauria |
Family: | † Parasuchidae |
Tribe: | † Mystriosuchini |
Genus: | † Mystriosuchus Fraas, 1896 |
Species | |
Mystriosuchus (meaning "spoon-crocodile") [1] is an extinct genus of phytosaur that lived in the Late Triassic (middle Norian) in Europe and Greenland. It was first named by Eberhard Fraas in 1896, and includes four species: M. planirostris (the type species), M. westphali, M. steinbergeri, and M. alleroq. [2] [3]
Mystriosuchus planirostris measured about 4 m (13 ft), according to a complete skeleton which was found in 1995. [4] The postcranial anatomy of the skeleton suggests that Mystriosuchus was more adapted to aquatic life than other known phytosaurs, possessing shorter and more paddle-like limbs as well as just two type of osteoderms as opposed to the higher diversity of other phytosaurs. [4] Cranial morphology is suggestive of a primarily fish eating diet, having long jaws like those of the modern gharials. [2] Several specimens have been recovered from marine fossil sites. [4] [5] A study on phytosaur microwear shows a preference towards softer invertebrates. [6]
M. planirostris, as the name implies, has a rather "plain" snout, without osseous ornamentation or crests. M. westphali, on the other hand, has multiple bony crests along the upper jaw, most prominently at the base and tip of the snout. As keratinous crests are known in phytosaurs, [7] it is possible that M. planirostris had soft tissue ornamentation.
Mystriosuchus possesses many vertebrae, with 25 in the neck and torso, two in the pelvis, and 74 in the tail. The vertebral column is complete and nearly all articulated, although a portion of the tail can only be seen from top view. The vertebrae behind the axis vertebra are platycoelous (one surface flat and one concave), and are approximately rectangular in shape. Because of incomplete preservation, it can't be distinguished where the neck meets the torso, although at least 17 of the 25 vertebrae come from the latter. The trunk vertebrae are lower and wider than the neck vertebrae, but are still lightly built. The pelvic vertebrae have wide ribs which attach to the ilium (largest pelvis bone). The tail is longer than the rest of the body, being 51% of the total length of the taxon. The first 17 vertebrae of the tail are similar to those of the neck and trunk, being platycoelous and subrectangular. Chevrons are present after the fourth vertebra, but are only loosely attached for the beginning of the tail. At the end of the tail the vertebrae become more slanted, and the chevrons form an inverted 'T' shape, which is not seen in other phytosaurs but in sauropterygians or some crocodilians. [4]
Mystriosuchus used to be placed in its own subfamily, Mystriosuchidae, [8] [9] but subsequent cladistic analysis grouped it with other members of Pseudopalatinae, despite having several physical differences from most of the genera in this group. [2] Originally considered to be a freshwater genus, a recent specimen from Northern Italy has shown that some Mystriosuchus specimens lived a completely marine life. [10] In their paper on Parasuchus , Christian Kammerer and colleagues noted that Mystriosuchini has priority over Pseudopalatinae, so synonymized Pseudopalatinae with Mystriosuchini. [11]
Below is a cladogram from Stocker (2012): [12]
Phytosauria |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Phytosaurs are an extinct group of large, mostly semiaquatic Late Triassic archosauriform reptiles. Phytosaurs belong to the order Phytosauria. and are sometimes referred to as parasuchians. Phytosauria, Parasuchia, Parasuchidae, and Phytosauridae have often been considered equivalent groupings containing the same species. Some recent studies have offered a more nuanced approach, defining Parasuchidae and Phytosauridae as nested clades within Phytosauria as a whole. Phytosaurs were long-snouted and heavily armoured, bearing a remarkable resemblance to modern crocodilians in size, appearance, and lifestyle, as an example of convergence or parallel evolution. The name "phytosaur" means "plant reptile", as the first fossils of phytosaurs were mistakenly thought to belong to plant eaters.
Paleorhinus is an extinct genus of widespread basal phytosaur known from the Late Triassic. The genus was named in 1904 based on the type species Paleorhinus bransoni, which is known from Wyoming and Texas in the United States. Another valid species, Paleorhinus angustifrons from Bavaria, Germany, is also commonly referred to the genus. Paleorhinus had a length of about 2.5 meters.
Parasuchus is an extinct genus of basal phytosaur known from the Late Triassic of Andhra Pradesh and Madhya Pradesh, India. At its most restricted definition, Parasuchus contains a single species, Parasuchus hislopi. Parasuchus hislopi is one of several species belonging to a basal grade of phytosaurs, typified by the genus Paleorhinus. Historically, Paleorhinus has been known from better-described fossils, and many species have been lumped into that genus. Parasuchus hislopi, despite being described earlier than Paleorhinus, was considered an undiagnostic chimera until new neotype fossils were described in the late 1970s. Parasuchus hislopi and the two unambiguously valid species of Paleorhinus are all closely related; some authors have historically described them all under the species Paleorhinus, while others place the two Paleorhinus species into Parasuchus according to the principle of priority.
Rutiodon is an extinct genus of mystriosuchine phytosaurs from the Late Triassic of the eastern United States. The type species of Rutiodon, Rutiodon carolinensis, encompasses a large number of skulls and assorted postcranial fossils discovered in the Cumnock Formation of North Carolina. Fossils referable to the species are also known from Pennsylvania, New Jersey, and Virginia. Rutiodon carolinensis is the most well-described species of phytosaur in eastern North America, though its validity as a natural taxon has been questioned. Some paleontologists also recognize a larger and more robust species, Rutiodon manhattanensis, which is known from teeth and postcranial fossils from New Jersey and Pennsylvania.
Nicrosaurus (/nɪkroʊˈsɔrəs/) is an extinct genus of phytosaur reptile existing during the Late Triassic period. Although it looked like a crocodile, it was not closely related to these creatures, instead being an example of parallel evolution. The main difference between Nicrosaurus and modern crocodiles is the position of the nostrils – Nicrosaurus's nostrils, or external nares, were placed directly in front of the forehead, whereas in crocodiles, the nostrils are positioned on the end of the snout. A 2013 study has also found that ilium of Nicrosaurus is quite distinctive from all other phytosaurs.
Doswellia is an extinct genus of archosauriform from the Late Triassic of North America. It is the most notable member of the family Doswelliidae, related to the proterochampsids. Doswellia was a low and heavily built carnivore which lived during the Carnian stage of the Late Triassic. It possesses many unusual features including a wide, flattened head with narrow jaws and a box-like rib cage surrounded by many rows of bony plates. The type species Doswellia kaltenbachi was named in 1980 from fossils found within the Vinita member of the Doswell Formation in Virginia. The formation, which is found in the Taylorsville Basin, is part of the larger Newark Supergroup. Doswellia is named after Doswell, the town from which much of the taxon's remains have been found. A second species, D. sixmilensis, was described in 2012 from the Bluewater Creek Formation of the Chinle Group in New Mexico; however, this species was subsequently transferred to a separate doswelliid genus, Rugarhynchos. Bonafide Doswellia kaltenbachi fossils are also known from the Chinle Formation of Arizona.
Megalancosaurus is a genus of extinct reptile from the Late Triassic Dolomia di Forni Formation and Zorzino Limestone of northern Italy, and one of the best known drepanosaurids. The type species is M. preonensis; a translation of the animal's scientific name would be "long armed reptile from the Preone Valley."
Drepanosaurs are a group of extinct reptiles that lived between the Carnian and Rhaetian stages of the late Triassic Period, approximately between 230 and 210 million years ago. The various species of drepanosaurid were characterized by specialized grasping limbs and often prehensile tails, adaptions for arboreal (tree-dwelling) and fossorial (digging) lifestyles, with some having also been suggested to be aquatic. Fossils of drepanosaurs have been found in Arizona, New Mexico, New Jersey, Utah, England, and northern Italy. The name is taken from the family's namesake genus Drepanosaurus, which means "sickle lizard," a reference to their strongly curved claws.
Angistorhinus is an extinct genus of phytosaur known from the Late Triassic period of Texas and Wyoming, United States. It was first named by Mehl in 1913 and the type species is Angistorhinus grandis. Other species from Texas and Wyoming, A. alticephalus, A. gracilis and A. maximus, are cospecific with the type species. Angistorhinus is known from the holotype UC 631, partial skull and lower jaws recovered from the Popo Agie Formation, Chugwater Group, Wyoming and from the associated paratype UM 531, a partial skull, TMM 31098-1, skull and lower jaws and ROM 7977, partial skull and lower jaws, recovered from the 'Pre-Tecovas Horizon' in the Dockum Group, Texas. A possible second species, A. talainti is known from the Triassic of Morocco. In 1995, Long and Murry created the new combination, Angistorhinus megalodon by synonymy for Brachysuchus. Hungerbühler and Sues (2001) hypothesised that Angistorhinus is a junior synonym of Rutiodon. However, in 2010 Michelle R. Stocker retained the validity of Brachysuchus and of A. grandis.
Smilosuchus is an extinct genus of leptosuchomorph parasuchid from the Late Triassic of North America.
Mystriosuchini, historically known as Pseudopalatinae, is an extinct tribe of derived phytosaurs in the clade Leptosuchomorpha. As with all other phytosaurs, mystriosuchins lived during Late Triassic. The name is derived from the genus Mystriosuchus.
Machaeroprosopus is an extinct genus of mystriosuchin leptosuchomorph phytosaur from the Late Triassic of the southwestern United States. M. validus, once thought to be the type species of Machaeroprosopus, was named in 1916 on the basis of three complete skulls from Chinle Formation, Arizona. The skulls have been lost since the 1950s, and a line drawing in the original 1916 description is the only visual record of the specimen. Another species, M. andersoni, was named in 1922 from New Mexico, and the species M. adamanensis, M. gregorii, M. lithodendrorum, M. tenuis, and M. zunii were named in 1930. Most species have been reassigned to the genera Smilosuchus, Rutiodon, or Phytosaurus. Until recently, M. validus was considered to be the only species that has not been reassigned. Thus, Machaeroprosopus was considered to be a nomen dubium or "doubtful name" because of the lack of diagnostic specimens that can support its distinction from other phytosaur genera. However, a taxonomic revision of Machaeroprosopus, conducted by Parker et al. in 2013, revealed that UW 3807, the holotype of M. validus, is not the holotype of Machaeroprosopus, while the species Machaeroprosopus buceros, Machaeroprosopus being a replacement name, with a fixed type species, for Metarhinus, is the combinatio nova of the type species of the genu: Belodon buceros. Therefore, the name Pseudopalatus must be considered a junior synonym of Machaeroprosopus, and all species of the former must be reassigned to the latter. This revised taxonomy was already accepted in several studies, including Stocker and Butler (2013). Stocker and Butler (2013) also treated M. andersoni as a valid species, and not a junior synonym of Machaeroprosopus buceros as was previously suggested by Long and Murry (1995).
Pravusuchus is an extinct genus of leptosuchomorph parasuchid phytosaur known from the Late Triassic of Arizona, United States. It contains a single species, Pravusuchus hortus, which is known from three specimens. These specimens were previously referred to Smilosuchus or to Leptosuchus, but Pravusuchus's autapomorphy, its phylogenetic position as well as a trait shared with mystriosuchins, justified the erection of a new taxon for the material.
Tarjadia is an extinct genus of erpetosuchid pseudosuchian, distantly related to modern crocodilians. It is known from a single species, T. ruthae, first described in 1998 from the Middle Triassic Chañares Formation in Argentina. Partial remains have been found from deposits that are Anisian-Ladinian in age. Long known mostly from osteoderms, vertebrae, and fragments of the skull, specimens described in 2017 provided much more anatomical details and showed that it was a fairly large predator. Tarjadia predates known species of aetosaurs and phytosaurs, two Late Triassic groups of crurotarsans with heavy plating, making it one of the first heavily armored archosaurs. Prior to 2017, most studies placed it outside Archosauria as a member of Doswelliidae, a family of heavily armored and crocodile-like archosauriforms. The 2017 specimens instead show that it belonged to the Erpetosuchidae.
Mesorhinosuchus is an extinct genus of basal phytosaur possibly known from the Early Triassic of Saxony-Anhalt, central-eastern Germany. It was first named by Otto Jaekel in 1910 and the type species is Mesorhinus fraasi. The generic name Mesorhinus was preoccupied by Mesorhinus piramydatus Ameghino, 1885, a macraucheniid mammal, which is now considered to be a junior synonym of Oxyodontherium. Thus, an alternative generic name, Mesorhinosuchus, was proposed by Oskar Kuhn in 1961. The genus is occasionally misspelled as Mesorhinosaurus, while Stocker and Butler (2013) recently misspelled its original generic name as Mesosuchus.
Protome is an extinct genus of parasuchid phytosaur from the Late Triassic of Arizona, represented by a single species, Protome batalaria. It is known from a single holotype incomplete, partially disarticulated skull and left lower jaw called PEFO 34034 from the Upper Lot's Wife beds, Sonsela Member of the Chinle Formation in Petrified Forest National Park. The skull was discovered in 2004 by Michelle Stocker and Bill Parker and was described by them as a specimen of Smilosuchus adamanensis. It was placed in the new genus Protome in 2012. The genus name Protome is the Greek word for an animal's face. The specific name batalaria is the Latin word for battleship, which is a reference to Battleship NW, the locality within Petrified Forest where the skull was found.
Parasuchidae is a clade of phytosaurs more derived than Diandongosuchus, a basal phytosaur. It encompasses nearly all phytosaurs, include early Parasuchus-grade forms as well as a more restricted clade of more specialized phytosaurs. This more restricted clade is traditionally known as the family Phytosauridae and more recently as the subfamily Mystriosuchinae.
Protorosauria is an extinct polyphyletic group of archosauromorph reptiles from the latest Middle Permian to the end of the Late Triassic of Asia, Europe and North America. It was named by the English anatomist and paleontologist Thomas Henry Huxley in 1871 as an order, originally to solely contain Protorosaurus. Other names which were once considered equivalent to Protorosauria include Prolacertiformes and Prolacertilia.
Diandongosuchus is an extinct genus of archosauriform reptile, possibly a member of the Phytosauria, known from the Middle Triassic of China. The type species Diandongosuchus fuyuanensis was named in 2012 from the Zhuganpo Formation of Yunnan Province. It is a marine species that shows similarities with another Chinese Triassic species called Qianosuchus mixtus, although it has fewer adaptations toward marine life. It was originally classified as the basal-most member of the pseudosuchian clade Poposauroidea. However, a subsequent study conducted by Stocker et al. indicated it to be the basalmost known phytosaur instead.