"Coelosaurus"antiquus Temporal range: Late Cretaceous, | |
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Holotype tibia | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Dinosauria |
Clade: | Saurischia |
Clade: | Theropoda |
Clade: | † Ornithomimosauria |
Family: | † Ornithomimidae |
Species: | † "Coelosaurus" antiquus |
Binomial name | |
"Coelosaurus"antiquus | |
Synonyms | |
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"Coelosaurus" antiquus ("antique hollow lizard") is a dubious species of theropod dinosaurs. It was named by Joseph Leidy in 1865 for two tibiae found in the Navesink Formation of New Jersey.
This species was later reclassified as a member of the genus Ornithomimus in 1979 by Donald Baird and John R. Horner as Ornithomimus antiquus, [1] and this was followed by some later researchers. [2] However, others have not followed this classification, and have noted that there is no justification for the classification of the New Jersey specimens in a genus known only from western North America. David Weishampel in 2004 considered "C." antiquus to be indeterminate among ornithomimosaurs, and therefore a nomen dubium . [3]
In 1979, Baird and Horner discovered that the name "Coelosaurus" was preoccupied by another dubious taxon (based on a single vertebra), named Coelosaurus by an anonymous author now known to be Richard Owen in 1854. [3]
Ornithomimid material known from the Severn Formation of Maryland and the Mooreville Chalk and Blufftown formations of Alabama and Georgia have also been assigned to this species. [4] A specimen once assigned to Coelosaurus that was discovered in the Merchantville Formation of Delaware during the 1970s has since been assigned to "Cryptotyrannus". [5]
Trachodon is a dubious genus of hadrosaurid dinosaur based on teeth from the Campanian-age Upper Cretaceous Judith River Formation of Montana, U.S. It is a historically important genus with a convoluted taxonomy that has been all but abandoned by modern dinosaur paleontologists.
Hadrosaurus is a genus of hadrosaurid ornithopod dinosaurs that lived in North America during the Late Cretaceous Period in what is now the Woodbury Formation about 78-80 Ma. The holotype specimen was found in fluvial marine sedimentation, meaning that the corpse of the animal was transported by a river and washed out to sea.
Ornithomimosauria are theropod dinosaurs which bore a superficial resemblance to the modern-day ostrich. They were fast, omnivorous or herbivorous dinosaurs from the Cretaceous Period of Laurasia, as well as Africa and possibly Australia. The group first appeared in the Early Cretaceous and persisted until the Late Cretaceous. Primitive members of the group include Nqwebasaurus, Pelecanimimus, Shenzhousaurus, Hexing and Deinocheirus, the arms of which reached 2.4 m (8 feet) in length. More advanced species, members of the family Ornithomimidae, include Gallimimus, Struthiomimus, and Ornithomimus. Some paleontologists, like Paul Sereno, consider the enigmatic alvarezsaurids to be close relatives of the ornithomimosaurs and place them together in the superfamily Ornithomimoidea.
Struthiomimus, meaning "ostrich-mimic", is a genus of ornithomimid dinosaurs from the late Cretaceous of North America. Ornithomimids were long-legged, bipedal, ostrich-like dinosaurs with toothless beaks. The type species, Struthiomimus altus, is one of the more common, smaller dinosaurs found in Dinosaur Provincial Park; their overall abundance—in addition to their toothless beak—suggests that these animals were mainly herbivorous or omnivorous, rather than purely carnivorous, if at all. Similar to the modern extant ostriches, emus, and rheas, ornithomimid dinosaurs likely lived as opportunistic omnivores, supplementing a largely plant-based diet with a variety of small mammals, reptiles, amphibians, insects, invertebrates, and anything else they could fit into their mouth, as they foraged.
Ornithomimus is a genus of ornithomimid theropod dinosaurs from the Campanian and Maastrichtian ages of Late Cretaceous Western North America. Ornithomimus was a swift, bipedal dinosaur which fossil evidence indicates was covered in feathers and equipped with a small toothless beak that may indicate an omnivorous diet. It is usually classified into two species: the type species, Ornithomimus velox, and a referred species, Ornithomimus edmontonicus. O. velox was named in 1890 by Othniel Charles Marsh on the basis of a foot and partial hand from the Denver Formation of Colorado. Another seventeen species have been named since then, though almost all of them have been subsequently assigned to new genera or shown to be not directly related to Ornithomimus velox. The best material of species still considered part of the genus has been found in Alberta, representing the species O. edmontonicus, known from several skeletons from the Horseshoe Canyon Formation. Additional species and specimens from other formations are sometimes classified as Ornithomimus, such as Ornithomimus samueli from the earlier Dinosaur Park Formation.
Dromiceiomimus is a genus of ornithomimid theropod from the Late Cretaceous of Alberta, Canada. The type species, D. brevitertius, is considered a synonym of Ornithomimus edmontonicus by some authors, while others consider it a distinct and valid taxon. It was a small ornithomimid that weighed about 135 kilograms (298 lb).
Claosaurus is a genus of hadrosauroid dinosaur that lived during the Late Cretaceous Period (Santonian-Campanian).
Gryposaurus was a genus of duckbilled dinosaur that lived about 80 to 75 million years ago, in the Late Cretaceous of North America. Named species of Gryposaurus are known from the Dinosaur Park Formation in Alberta, Canada, and two formations in the United States: the Lower Two Medicine Formation in Montana and the Kaiparowits Formation of Utah. A possible additional species from the Javelina Formation in Texas may extend the temporal range of the genus to 66 million years ago.
Archaeornithomimus is a genus of ornithomimosaurian theropod dinosaur that lived in Asia during the Late Cretaceous period, around 96 million years ago in the Iren Dabasu Formation.
Dryptosaurus is a genus of basal eotyrannosaurian theropod dinosaur that lived on the island continent of Appalachia approximately 67 million years ago during the end of the Maastrichtian age of the Late Cretaceous period. Dryptosaurus was a large, bipedal, ground-dwelling carnivore that could grow up to 7.5 metres (25 ft) long and weigh up to 1.5 metric tons. Although it is now largely unknown outside of academic circles, the famous 1897 painting of the genus by Charles R. Knight made Dryptosaurus one of the more widely known dinosaurs of its time, in spite of its poor fossil record. First described by Edward Drinker Cope in 1866 and later renamed by Othniel Charles Marsh in 1877, Dryptosaurus is among the very first theropod dinosaurs ever known to science.
Valdoraptor is a genus of theropod dinosaur from the Early Cretaceous. Its fossils were found in England. It is known only from bones of the feet. The holotype, BMNH R2559, was found near Cuckfield in layers of the Tunbridge Wells Sand Formation dating from the late Valanginian. The specimen is damaged lacking parts of the upper and lower ends. It has a conserved length of 215 millimetres (8.5 in) and an estimated length of 240 millimetres (9.4 in). This genus is paleontologically significant for being the first ornithomimosaur specimen known from England and represents the earliest record of ornithomimosaurs.
Hypsibema is an extinct genus of hadrosaurid dinosaurs from the Late Cretaceous (Campanian-aged) Black Creek Group of North Carolina. The type species is H. crassicauda, with a potential second species in H. missouriensis.
Ornithotarsus is a genus of hadrosaurid ornithopod dinosaurs that lived in North America during the Late Cretaceous Period in what is now the Merchantville Formation about 84 million to 78 million years ago.
Nedcolbertia is a genus of theropod dinosaur from the Early Cretaceous Period of North America.
The Navesink Formation is a 66 to 70 mya greensand glauconitic marl and sand geological formation in New Jersey. It is known for its Cretaceous period fossil shell beds and dinosaur bones.
During most of the Late Cretaceous the eastern half of North America formed Appalachia, an island land mass separated from Laramidia to the west by the Western Interior Seaway. This seaway had split North America into two massive landmasses due to a multitude of factors such as tectonism and sea-level fluctuations for nearly 40 million years. The seaway eventually expanded, divided across the Dakotas, and by the end of the Cretaceous, it retreated towards the Gulf of Mexico and the Hudson Bay. This left the island masses joined in the continent of North America as the Rocky Mountains rose. From the Cenomanian to the end of the Campanian ages of the Late Cretaceous, Appalachia was separated from the rest of North America. As the Western Interior Seaway retreated in the Maastrichtian, Laramidia and Appalachia eventually connected. Because of this, its fauna was isolated, and developed very differently from the tyrannosaur, ceratopsian, hadrosaurid, pachycephalosaur and ankylosaurid dominated fauna of the western part of North America, known as "Laramidia".
"Dryosaurus" grandis is a dubious species of ornithomimosaur dinosaur known from remains found in the Arundel Formation of Maryland.
The Tar Heel Formation is a geologic formation in North Carolina. It preserves fossils, including amber dating back to the Cretaceous period. A locality known as Phoebus Landing, has been dated to 78.5-77.1 Ma.
This timeline of ornithomimosaur research is a chronological listing of events in the history of paleontology focused on the ornithomimosaurs, a group of bird-like theropods popularly known as the ostrich dinosaurs. Although fragmentary, probable, ornithomimosaur fossils had been described as far back as the 1860s, the first ornithomimosaur to be recognized as belonging to a new family distinct from other theropods was Ornithomimus velox, described by Othniel Charles Marsh in 1890. Thus the ornithomimid ornithomimosaurs were one of the first major Mesozoic theropod groups to be recognized in the fossil record. The description of a second ornithomimosaur genus did not happen until nearly 30 years later, when Henry Fairfield Osborn described Struthiomimus in 1917. Later in the 20th century, significant ornithomimosaur discoveries began occurring in Asia. The first was a bonebed of "Ornithomimus" asiaticus found at Iren Debasu. More Asian discoveries took place even later in the 20th century, including the disembodied arms of Deinocheirus mirificus and the new genus Gallimimus bullatus. The formal naming of the Ornithomimosauria itself was performed by Rinchen Barsbold in 1976.