| Antarctanax Temporal range: Early Triassic ~ | |
|---|---|
Scientific classification  | |
| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Reptilia |
| Clade: | Archosauromorpha |
| Clade: | Archosauriformes |
| Genus: | † Antarctanax Peecook et al. 2019 |
| Type species | |
| †Antarctanax shackletoni Peecook et al. 2019 | |
Antarctanax is a genus of basal archosauriform that during the Triassic lived in Antarctica. The type species is Antarctanax shackletoni. It was a reptile around the size of an iguana. [1]
During a paleontological expedition to the Transantarctic Mountains in 2010 and 2011, a small skeleton was discovered at the Graphite Peak. [1]
In 2019, the type species Antarctanax shackletoni was named and described by Brandon Robert Peecook, Roger Malcolm Harris Smith and Christian Alfred Sidor. The generic name combines a reference to Antarctica — itself derived from Greek anti, "opposite of", and arktikos, "of the Bear" — with a Greek anax, "ruler", a reference to the Archosauria, the "Ruling Reptiles". The specific name honours Ernest Shackleton, the polar explorer who named the Beardmore Glacier which runs along the Graphite Peak. [1]
The holotype, UWBM 95531, was found in a layer of the lower Fremouw Formation, which dates to the Early Triassic. It consists of a partial skeleton lacking the skull. It contains eight vertebrae of the neck or back, ribs, the left humerus, all five metatarsals of the left foot, phalanges, among them the claws, of the left foot, and the almost complete right foot. Apart from the feet, the skeleton is largely disarticulated. It represents an adult individual. [1]
Antarctanax was about the size of an iguana, 1.2 to 1.5 m (4 to 5 ft) long. [2]
The describing authors indicated a unique combination of traits that in themselves are not unique. These traits prove that Antarctanax is a distinct taxon. The cervicodorsal vertebrae, those spanning the rear neck and front back, have per side a lamina centrodiapophysealis anterior, a ridge running on the front underside of the side process towards the vertebral body. The cervicodorsal vertebrae have per side a lamina prezygodiapophysealis, a ridge running from the side process to the front articulation process. The cervicodorsal vertebrae have per side a lamina postzygodiapophysealis, a ridge running from the side process to the rear articulation process. The cervicodorsal vertebrae lack a lamina centrodiapophyseal posterior, a ridge running on the rear underside of the side process towards the vertebral body. The neck vertebrae have no keels on the underside. The neck vertebrae have deep pits to the side of the base of the neural spine. The back vertebrae have deep pits to the side of the base of the neural spine. The fourth metatarsal is more than 30% longer than the third metatarsal. [1]
Antarctanax was, within the larger Archosauromorpha, placed in the Archosauriformes. A cladistic analysis showed that it had a more derived position than the Proterosuchidae. It was in a polytomy with Fugusuchus and Sarmatosuchus , all three forms being more basal than Cuyosuchus , the Erythrosuchidae and the Eucrocopoda. [1] The derived position of Antarctanax indicates that several more basal archosauromorph groups must have ghost lineages dating back to the Late Permian. [2]
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.
Tanystropheus is an extinct genus of archosauromorph reptile which lived during the Triassic Period in Europe, Asia, and North America. It is recognisable by its extremely elongated neck, longer than the torso and tail combined. The neck was composed of 13 vertebrae strengthened by extensive cervical ribs. Tanystropheus is one of the most well-described non-archosauriform archosauromorphs, known from numerous fossils, including nearly complete skeletons. Some species within the genus may have reached a total length of 6 meters (20 ft), making Tanystropheus the longest non-archosauriform archosauromorph as well. Tanystropheus is the namesake of the family Tanystropheidae, a clade collecting many long-necked Triassic archosauromorphs previously described as "protorosaurs" or "prolacertiforms".
Euhelopus is a genus of sauropod dinosaur that lived between 145 and 133 million years ago during the Berriasian and Valanginian stages of the Early Cretaceous in what is now Shandong Province in China. It was a large quadrupedal herbivore. Like sauropods such as brachiosaurs and titanosaurs, Euhelopus had longer forelegs than hind legs. This discovery was paleontologically significant because it represented the first dinosaur scientifically investigated from China: seen in 1913, rediscovered in 1922, and excavated in 1923 and studied by T'an during the same year. Unlike most sauropod specimens, it has a relatively complete skull.
Macroplata is an extinct genus of Early Jurassic rhomaleosaurid plesiosaur which grew up to 4.65 metres (15.3 ft) in length. Like other plesiosaurs, Macroplata probably lived on a diet of fish, using its sharp needle-like teeth to catch prey. Its shoulder bones were fairly large, indicating a powerful forward stroke for fast swimming. Macroplata also had a relatively long neck, twice the length of the skull, in contrast to pliosaurs.
Tasmaniosaurus is an extinct genus of archosauromorph reptile known from the Knocklofty Formation of West Hobart, Tasmania, Australia. The type species is T. triassicus. This genus is notable not only due to being one of the most complete Australian Triassic reptiles known, but also due to being a very close relative of Archosauriformes. Once believed to be a proterosuchid, this taxon is now believed to have been intermediate between advanced non-archosauriform archosauromorphs such as Prolacerta, and basal archosauriforms such as Proterosuchus. Features traditionally used to define Archosauria and later Archosauriformes, such as the presence of an antorbital fenestra and serrated teeth, are now known to have evolved prior to those groups due to their presence in Tasmaniosaurus.
Qianosuchus is an extinct genus of aquatic poposauroid archosaur from the middle Triassic (Anisian) Guanling Formation of Pan County, China. It is represented by two nearly complete skeletons and a crushed skull preserved in the limestone. Qianosuchus was at least 3 metres long, and had several skeletal adaptations which indicate a semi-marine lifestyle, similar to modern-day saltwater crocodiles. These adaptations have not been seen in any other archosaur from the Triassic.
Yarasuchus is an extinct genus of avemetatarsalian archosaur that lived during the Anisian stage of the Middle Triassic of India. The genus was named and described in 2005 from a collection of disarticulated but fairly complete fossil material found from the Middle Triassic Yerrapalli Formation. The material is thought to be from two individuals, possibly three, with one being much more complete and articulated than the other. The type and only species is Y. deccanensis. Yarasuchus was a quadruped roughly 2–2.5 metres (6.6–8.2 ft) long, with an elongated neck and tall spines on its vertebrae. Unlike other quadrupedal Triassic reptiles, the limbs and shoulders of Yarasuchus were slender, and more like those of ornithodirans.
Vancleavea is a genus of extinct, armoured, non-archosaurian archosauriforms from the Late Triassic of western North America. The type and only known species is V. campi, named by Robert Long & Phillip A Murry in 1995. At that time, the genus was only known from fragmentary bones including osteoderms and vertebrae. However, since then many more fossils have been found, including a pair of nearly complete skeletons discovered in 2002. These finds have shown that members of the genus were bizarre semiaquatic reptiles. Vancleavea individuals had short snouts with large, fang-like teeth, and long bodies with small limbs. They were completely covered with bony plates known as osteoderms, which came in several different varieties distributed around the body. Phylogenetic analyses by professional paleontologists have shown that Vancleavea was an archosauriform, part of the lineage of reptiles that would lead to archosaurs such as dinosaurs and crocodilians. Vancleavea lacks certain traits which are present in most other archosauriforms, most notably the antorbital, mandibular and supratemporal fenestrae, which are weight-saving holes in the skulls of other taxa. However, other features clearly support its archosauriform identity, including a lack of intercentra, the presence of osteoderms, an ossified laterosphenoid, and several adaptations of the femur and ankle bones. In 2016, a new genus of archosauriform, Litorosuchus, was described. This genus resembled both Vancleavea and more typical archosauriforms in different respects, allowing Litorosuchus to act as a transitional fossil linking Vancleavea to less aberrant archosauriforms.
Teraterpeton is an extinct genus of trilophosaurid archosauromorphs. It is known from a partial skeleton from the Late Triassic Wolfville Formation of Nova Scotia, described in 2003. It has many unique features seen in no other related form, including an elongated, toothless snout and large openings for the nostrils. Because of this, Teraterpeton was originally placed in its own family, Teraterpetidae, related to Trilophosaurus. Newer studies generally place it within Trilophosauridae.
Jesairosaurus is an extinct genus of early archosauromorph reptile known from the Illizi Province of Algeria. It is known from a single species, Jesairosaurus lehmani. Although a potential relative of the long-necked tanystropheids, this lightly-built reptile could instead be characterized by its relatively short neck as well as various skull features.
Eorasaurus is an extinct genus of archosauromorph reptile known from the middle Late Permian of Tatarstan, European Russia. It contains a single species, Eorasaurus olsoni. When originally described by Sennikov (1997), Eorasaurus was identified as an early archosauromorph and assigned to the family Protorosauridae, Ezcurra et al. (2014) and Ezcurra (2016) later reclassified Eorasaurus and placed it within the group Archosauriformes. Eorasaurus is based solely on scant fossil material from the neck region, and is thus considered an unstable taxon in phylogenetic analyses. If Eorasaurus is an archosauriform, it would be the oldest known member of the group and would pre-date the previous record holder.
This glossary explains technical terms commonly employed in the description of dinosaur body fossils. Besides dinosaur-specific terms, it covers terms with wider usage, when these are of central importance in the study of dinosaurs or when their discussion in the context of dinosaurs is beneficial. The glossary does not cover ichnological and bone histological terms, nor does it cover measurements.
Dracoraptor is a genus of coelophysoid dinosaur that lived during the Hettangian stage of the Early Jurassic Period of what is now Wales dated at 201.3 ± 0.2 million years old.
Ozimek is a genus of sharovipterygid archosauromorph reptile, known from Late Triassic deposits in Poland and closely related to the Kyrgyzstani Sharovipteryx. It contains one species, O. volans, named in 2016 by Jerzy Dzik and Tomasz Sulej. Like Sharovipteryx, Ozimek had long, slender limbs with the hindlimbs longer than the forelimbs; the hindlimbs likely supported gliding membranes as fossilized in Sharovipteryx. Another unusual characteristic was the shoulder girdle, where the massive coracoids formed a shield-like structure covering the bottom of the shoulder region that would have limited mobility. In other respects, such as its long neck, it was a typical member of the non-natural grouping Protorosauria. Phylogenetic analysis has indicated that it, possibly along with Sharovipteryx, may have been an unusual member of the protorosaur group Tanystropheidae, although further study of its anatomy is needed to resolve its precise relationships.
Vouivria is a genus of herbivorous sauropod dinosaur, belonging to the Brachiosauridae, that lived in the area of present France during the Late Jurassic. The type species is Vouivria damparisensis.
Pectodens is an extinct genus of archosauromorph reptile which lived during the Middle Triassic in China. The type and only species of the genus is P. zhenyuensis, named by Chun Li and colleagues in 2017. It was a member of the Archosauromorpha, specifically part of the unnatural grouping Protorosauria. However, an unusual combination of traits similar and dissimilar to other protorosaurs initially led to confusion over its evolutionary relationships. In 2021, it was placed in a newly-established group, Dinocephalosauridae, along with its closest relative Dinocephalosaurus.
Rhombopholis is an extinct genus of archosauromorph reptile known from England. The type species of Rhombopholis is Rhombopholis scutulata. Specimens of this genus were collected from the Leamington quarry, near Warwick. This locality belongs to the Bromsgrove Sandstone Formation, which is dated to the Anisian age of the Middle Triassic, approximately 245 million years ago.
Mnyamawamtuka is a genus of lithostrotian titanosaur sauropod dinosaur from the Cretaceous Galula Formation in Tanzania. The type and only species is M. moyowamkia.
Boreopricea is an extinct genus of archosauromorph reptile from the Early Triassic of arctic Russia. It is known from a fairly complete skeleton discovered in a borehole on Kolguyev Island, though damage to the specimen and loss of certain bones has complicated study of the genus. Boreopricea shared many similarities with various other archosauromorphs, making its classification controversial. Various studies have considered it a close relative of Prolacerta, tanystropheids, both, or neither. Boreopricea is unique among early archosauromorphs due to possessing contact between the jugal and squamosal bones at the rear half of the skull.
