Archaeornithomimus Temporal range: Late Cretaceous, ~ | |
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Archaeornithomimus asiaticus skeleton mounted at the Paleozoological Museum of China. | |
Scientific classification ![]() | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Dinosauria |
Clade: | Saurischia |
Clade: | Theropoda |
Clade: | † Ornithomimosauria |
Family: | † Ornithomimidae |
Genus: | † Archaeornithomimus Russell, 1972 |
Species: | †A. asiaticus |
Binomial name | |
†Archaeornithomimus asiaticus | |
Archaeornithomimus (meaning "ancient bird mimic") 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.
In 1923, during the American Museum of Natural History expedition by Roy Chapman Andrews to Inner Mongolia, Peter Kaisen discovered numerous theropod remains in three quarries. They consist of the largely disarticulated remains of several individuals and material of the skull and the lower jaws is lacking. These were named and shortly described by Charles Whitney Gilmore in 1933 as a new species of Ornithomimus : Ornithomimus asiaticus. The specific name refers to the Asian provenance. [1] The species was placed in the new genus Archaeornithomimus by Dale Russell in 1972, making Archaeornithomimus asiaticus the type species of the genus. The generic name combines that of Ornithomimus with a Greek ἀρχαῖος (archaios), "ancient", because Russell believed that the layers in which Archaeornithomimus was found dated to the Cenomanian-Turonian ages, about 95 million years ago, making it one of the oldest ornithomimids known at the time. [2] Gilmore had not assigned a holotype specimen; in 1990, David Smith and Peter Galton in the first comprehensive description of the fossils, choose specimen AMNH 6565, a foot, as the lectotype. [3] The fossils were found in the Iren Dabasu Formation, which has been dated to the Cenomanian age, around 95.8 ± 6.2 million years ago. [4]
Foot bones found in the Early Cretaceous Arundel Formation of Maryland were referred by Othniel Charles Marsh to Allosaurus medius in 1888. [5] In 1911, Richard Swann Lull named these as a new species of Dryptosaurus : Dryptosaurus grandis. [6] In 1920, Gilmore renamed them to a new species of Ornithomimus. However, because Ornithomimus grandis already existed, he renamed the species Ornithomimus affinis. [7] In 1972, Dale Russell renamed them as a second species of Archaeornithomimus (A. affinis), [2] but other authors considered this taxon a nomen dubium in both editions of The Dinosauria. [8] [9] In 1990, Smith and Galton concluded that the remains were not ornithomimosaurian and came from some other small theropod, [3] while the describers of other ornithomimosaurs ( Kinnareemimus , Arkansaurus and Paraxenisaurus ) suggested that "O." affinis does belong to an indeterminate ornithomimosaur. [10] [11] [12]
In 1995, Nesov named a new species of ornithomimosaur from the Bissekty Formation (Turonian) of Uzbekistan as Archaeornithomimus bissektensis, based on the holotype N 479/12457, a femur of a juvenile, along with other referred specimens including the metatarsals. [13] However, the affinity of A. bissektensis was generally doubted or not mentioned by subsequent studies. [14] [15] [16] In 2025, Averianov and Sues assigned this taxon to the new genus Dzharacursor . [17]
Archaeornithomimus was a medium sized ornithomimosaur, reaching 3.4 m (11 ft) long and weighing over 71.5 kilograms (158 lb). [18] [19] Solid evidence coming from other ornithomimosaurian relatives suggest that Archaeornithomimus was a feathered animal, with very ratite-like feathers [20] [21] and equipped with a keratinous beak. [22] [23]
The hindlimbs were robustly built. The third metatarsal was not pinched at the upper end, so the foot was not arctometatarsalian. [3] The cervical vertebrae are highly pneumatized with very complex internal chambers across the neural arches and the centrum (body of the vertebra), indicating the presence of cervical air sacs. The anterior dorsal and some caudal vertebrae features some degree of pneumacity, however, the sacral vertebrae are apneumatic. [15] In a 2001 study conducted by Bruce Rothschild and other paleontologists, 229 foot bones referred to Archaeornithomimus were examined for signs of stress fracture, but none were found. [24]
Russell assigned Archaeornithomimus to the Ornithomimidae. [2] Recent cladistic analyses either confirm this or recover the species outside of the Ornithomimidae, basal in the Ornithomimosauria. During the description of Hesperornithoides , an extensive Coelurosauria phylogenetic analysis (also known as the Lori matrix) was conducted in order to determine the position of this paravian. Here, Archaeornithomimus was recovered within the Garudimimidae being a relative of Arkansaurus : [16]
Ornithomimosauria |
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The remains of Archaeornithomimus were found in the Iren Dabasu Formation, which dates back to the Cenomanian stage about 96 million years ago during the Late Cretaceous period. [4] The environments present on the formation were mainly large floodplain terrains with braided rivers and meanders [25] [26] that were connected to the ocean, [27] supporting extensive vegetation as seen on the palaeosol development and the numerous remains from herbivorous dinosaurs such as hadrosauroids. [25]
Like other members of the Ornithomimosauria, Archaeornithomimus was likely an omnivore equipped with a horny beak, eating everything from small mammals, to plants and fruit, to eggs, and even hatchlings of other Asian dinosaurs. [22] [23]
Other dinosaurs that co-existed with Archaeornithomimus in the formation included other theropods, such as Alectrosaurus , Erliansaurus , Gigantoraptor and Neimongosaurus . Herbivorous dinosaurs were represented by Bactrosaurus , Gilmoreosaurus and Sonidosaurus . [28]
Gallimimus is a genus of theropod dinosaur that lived in what is now Mongolia during the Late Cretaceous period, about seventy million years ago (mya). Several fossils in various stages of growth were discovered by Polish-Mongolian expeditions in the Gobi Desert of Mongolia during the 1960s; a large skeleton discovered in this region was made the holotype specimen of the new genus and species Gallimimus bullatus in 1972. The generic name means "chicken mimic", referring to the similarities between its neck vertebrae and those of the Galliformes. The specific name is derived from bulla, a golden capsule worn by Roman youth, in reference to a bulbous structure at the base of the skull of Gallimimus. At the time it was named, the fossils of Gallimimus represented the most complete and best preserved ornithomimid material yet discovered, and the genus remains one of the best known members of the group.
Anserimimus is a genus of ornithomimid theropod dinosaur, from the Late Cretaceous Period of what is now Mongolia. It was a lanky, fast-running animal, possibly an omnivore. From what fossils are known, it probably closely resembled other ornithomimids, except for its more powerful forelimbs.
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. 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).
Deinocheirus is a genus of large ornithomimosaur that lived during the Late Cretaceous around 70 million years ago. In 1965, a pair of large arms, shoulder girdles, and a few other bones of a new dinosaur were first discovered in the Nemegt Formation of Mongolia. In 1970, this specimen became the holotype of the only species within the genus, Deinocheirus mirificus; the genus name is Greek for "horrible hand". No further remains were discovered for almost fifty years, and its nature remained a mystery. Two more complete specimens were described in 2014, which shed light on many aspects of the animal. Parts of these new specimens had been looted from Mongolia some years before, but were repatriated in 2014.
Garudimimus is a genus of ornithomimosaur that lived in Asia during the Late Cretaceous. The genus is known from a single specimen found in 1981 by a Soviet-Mongolian paleontological expedition in the Bayan Shireh Formation and formally described in the same year by Rinchen Barsbold; the only species is Garudimimus brevipes. Several interpretations about the anatomical traits of Garudimimus were made in posterior examinations of the specimen, but most of them were criticized during its comprehensive redescription in 2005. Extensive undescribed ornithomimosaur remains at the type locality of Garudimimus may represent additional specimens of the genus.
Alectrosaurus is a genus of tyrannosauroid theropod dinosaur that lived in Asia during the Late Cretaceous period, about some 96 million years ago in what is now the Iren Dabasu Formation.
The Bayan Shireh Formation is a geological formation in Mongolia, that dates to the Cretaceous period. It was first described and established by Vasiliev et al. 1959.
Ornithomimidae is an extinct family of theropod dinosaurs which bore a superficial resemblance to modern ostriches. Ornithomimids were fast, omnivorous or herbivorous dinosaurs known mainly from the Late Cretaceous Period of Laurasia, though they have also been reported from the Lower Cretaceous Wonthaggi Formation of Australia.
Shuvosaurus is a genus of beaked, bipedal poposauroid pseudosuchian from the Late Triassic of western Texas. Despite superficially resembling a theropod dinosaur, especially the ostrich-like ornithomimids, it is instead more closely related to living crocodilians than to dinosaurs. Shuvosaurus is known by the type and only species S. inexpectatus, and is closely related to the very similar Effigia within the clade Shuvosauridae. Shuvosaurus was originally described from a restored skull and very few fragmentary postcranial bones as a probable ornithomimosaur, or at least a very ornithomimosaur-like early theropod. The true pseudosuchian affinities of Shuvosaurus were only recognised after the discovery of Effigia linked the skull of Shuvosaurus with similar poposauroid skeletal remains found in the same quarry.
"Coelosaurus" antiquus 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.
Gigantoraptor is a genus of large oviraptorosaur dinosaur that lived in Asia during the Late Cretaceous period. It is known from the Iren Dabasu Formation of Inner Mongolia, where the first remains were found in 2005.
The Iren Dabasu Formation is a Late Cretaceous geologic formation in the Iren Nor region of Inner Mongolia. Dinosaur remains diagnostic to the genus level are among the fossils that have been recovered from the formation. The formation was first described and defined by Henry Fairfield Osborn in 1922 and it is located in the Iren Nor region of China.
"Dryosaurus" grandis is a dubious species of ornithomimosaur dinosaur known from remains found in the Arundel Formation of Maryland.
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.
Aepyornithomimus is a genus of ornithomimid theropod dinosaur from the Late Cretaceous Djadokhta Formation in Mongolia. It lived in the Campanian, around 75 million years ago, when the area is thought to have been a desert. The type and only species is A. tugrikinensis.
Dzharacursor is a genus of ornithomimid theropod dinosaurs from the Late Cretaceous Bissekty Formation of Uzbekistan. The type and only species is Dzharacursor bissektensis, originally assigned to the genus Archaeornithomimus.
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