This list of specimens is a comprehensive catalogue of all the type specimens and their scientific designations for each of the genera and species that are included in the clade ornithopoda.
Ornithopoda is a clade of ornithischiandinosaurs that includes some of the most common and widespread Mesozoic animals including iguanodonts, hadrosaurs, and some animals formerly called "hypsilophodonts". The clade was named by Othniel Charles Marsh in 1881[1] and roughly means "bird feet". This name is reflective of the tridactyl feet of most ornithopods, which are superficially similar to many birds. Ornithopods were among the first dinosaurs known to scientists. The first species to be described was Iguanodon, which was described in 1825 by Sir Richard Owen.[2] Today, they collectively comprise the most diverse ornithischian group.[3][4]
The exact origin of ornithopods is uncertain. Some authors consider very primitive ornithischians like Nanosaurus, Hypsilophodon, and Jeholosaurus to be ornithopods,[5] while others do not.[6] Most ornithischians were ancestrally small and bipedal, which makes the taxonomy of these species complex and uncertain.[7][8] However, they are generally agreed to have originated by the middle Jurassic and shortly thereafter, they proliferated to most of the world's continents.[9] Ornithischians in general, but especially ornithopods, saw a large degree of diversification during the early Cretaceous.[10] This culminated in the proliferation of the giant hadrosaurs across the Northern Hemisphere and even into Africa[11] and South America.[12] Ornithopod remains are known from all of the world's continents, including Antarctica.[13]
Scope and Terminology
This list will include the typefossils of each ornithopod species. In paleontology, a type specimen is one which is definitionally a member of a biological taxon. Additional specimens can only be "referred" to these taxa if an expert deems them sufficiently similar to the type and publishes that opinion in the scientific literature.
There is no complete, canonical list of all dinosaur taxa or holotype specimens. Attempts are regularly published in the form of books, such as the Princeton Field Guide to Dinosaurs by Gregory Paul[3] and Dinosaurs: The Most Complete, Up-to-Date Encyclopedia for Dinosaur Lovers of All Ages by Thomas Holtz and Luis Rey.[4] Where appropriate, The The Paleobiology Database and Fossilworks, which are both online databases of named fossil taxa, are used to supplement the entries from published encyclopedias which are missing or data-deficient.
This list will also be updated regularly as new scientific descriptions are published and new taxa are named. The most recently named ornithopod is Minqaria bata, which was described in February 2024 by Nicholas R. Longrich, Xabier Pereda-Suberbiola, Nathalie Bardet, and Nour-Eddine Jalil.[14]
Type System
Types are also used to diagnose higher-level taxa than an individual. One individual might represent the "type specimen" of a particular species. This species would in turn represent the "type species" of a particular genus, unless it is referred to a previously described genus. Most dinosaur genera are monospecific, therefore most type specimens are also the type species of their respective genera. On this list, the type species of a genus is only noted when it belongs to a genus with multiple referred species, such as Dryosaurus or Parasaurolophus. Furthermore, when an animal is different enough from its close relatives that it is given its own family, it is conventional in dinosaur systematics to name a family after the first described, most famous, or most abundant genus assigned to it. Therefore, on this list, the type species of any type genus for a family or sub-family level taxon is also noted when appropriate.
There are several different varieties of type specimen when referring to fossil animals:[15]
Holotype: This is the most common and simplest form of type specimen. A holotype is the first material of a fossil taxon that is described in the scientific literature. In order to qualify as a true holotype, all of the fossils of the type must belong to the same individual animal. All type specimens on this list are holotypes, unless otherwise indicated.
Paratype(s): These are described in the same publication as the holotype. A paratype is designated when the fossil material is diagnostic enough to belong to the same species as the holotype, but it is not from the same individual animal. In these cases, the holotype and paratype(s) are collectively called the "type series" for that taxon. On this list, paratypes are noted in the same entry as their associated holotype.
Neotype: When a holotype specimen is lost, destroyed, or otherwise unable to be studied further by scientists, a new type specimen for that taxon is required in order to identify future material. On this list, neotypes are only given their own entries when the holotype was never formally given a specimen number, otherwise they are noted in the entry for the holotype.
Syntype(s): This is a type series in which no single specimen is selected to serve as a holotype, nor are any designated as paratypes. This is typically done if the fossil material is believed to be from multiple animals, but none of the individual animals were well-preserved enough to provide a complete list of diagnostic characters. These are also sometimes called "cotypes" in publications, although this is discouraged by the ICZN.
Lectotype: When a single type specimen from a series of syntypes is designated as the new primary type specimen in a subsequent publication, this is considered to be a lectotype. On this list, lectotypes are given their own entries.
Paralectotype(s): When a lectotype is designated from a series of syntypes, the remaining syntypes become paralectotypes as part of a reorganized type series. On this list, paralectotypes are noted alongside the list entry for the lectotype of their respective series.
Plastotype: Sometimes, if a cast of a type specimen is made and the original type specimen is lost or destroyed, the cast can be used for the purposes of diagnostic referral to a taxon. Plastotypes are only given their own entries on this list if the holotype was not given a specimen number. Otherwise, they are noted alongside the entry for the holotype.
Topotype: When a specimen is discovered from the same locality as a holotype specimen it may be given a new specimen number. If the second specimen is later determined to belong to the same animal as the holotype after the holotype has been described, it becomes a topotype.
All name-bearing type specimens (i.e. holotypes, lectotypes, neotypes, and syntypes) have unique entries on this list, and non-name-bearing types (i.e. paratypes, paralectotypes, topotypes, and holotypes that have been subsumed by a neotype) are noted alongside their name-bearing counterpart.
Validity
Some described species are later determined to be invalid by subsequent scientific publications. However, invalid species are sometimes resurrected, such as in the case of Brontosaurus,[16] and sometimes the validity of a species can be controversial among researchers (e.g. the case of Torosaurus and Triceratops[17][18]). For the purposes of neutrality and completeness, all described species and genera of marginocephalians are included, even those that have been considered invalid in subsequent scientific publications.
Junior synonym: A name which describes the same taxon as a previously published name. If two or more taxa are formally designated and the type specimens are later assigned to the same taxon, the first to be published (in chronological order) is the senior synonym, and all other instances are junior synonyms. Senior synonyms are generally used, except by special decision of the ICZN, but junior synonyms cannot be used again, even if deprecated. Junior synonymy is often subjective, unless the genera described were both based on the same type specimen.
Nomen dubium (Latin for "dubious name"): A name describing a fossil with no unique diagnostic features. T his can be an extremely controversial designation, and as such, they are only notated when their supposedly dubious status has been formally published. Furthermore, if the scientific community has yet to reach a consensus on the validity of a name or taxon, the ongoing nature of the controversy will be stated.
Nomen nudum (Latin for "naked name"): A name that has appeared in print but has not yet been formally published by the standards of the ICZN. Nomina nuda (the plural form) are invalid, and are not included on this list.
Preoccupied name: A name that is formally published, but which has already been used for another taxon. This second use is invalid (as are all subsequent uses) and the name must be replaced.
Omissions
Some ornithopod taxa are not included on this list. Nomina nuda are not included because a type does not become recognized by the ICZN until it is published in a scientific journal with a full description.
Some misidentified taxa are also not included so long as there is a scientific consensus with regard to the specimen in question. If a specimen is later referred to a taxon outside ornithopoda, it is not included on this list. However, specimens that are identified as ornithopods in publications subsequent to their initial description are included under the name they are given within ornithopoda.
Referred taxa are only included on the list as separate entries when their initial description includes a unique type specimen.
In the case of specimens with uncertain taxonomic affinity, they will be excluded unless they are considered ornithopods by the most recently published nomenclatural study of ornithischian dinosaurs, published in 2021.[8] This excludes animals like Jeholosaurus and Thescelosaurus, which are considered basal neornithischians by the authors. This is the same definition used on the article "Ornithopoda".
List of Specimens
Binomial name: All animals species are given a unique binomial name, typically consisting of Latin or Greek words which are used to formally and scientifically identify each species.
Catalogue number: In most museum collections, each fossil specimen will be given a unique catalogue number which is published with the description of the fossils after they are prepared. This serves as a formal name for every single described fossil so that authors are able to refer to individual fossil discoveries in the scientific literature by name.
Institution: Most published fossils are stored in museum collections or at universities. This is also true of type specimens, many of which are on display in museums around the world. If a type specimen has been lost, the last known location of the type is listed.
Age: The geological stage from which the specimen was recovered is listed, when it is known. The exact age of some geological formations is not known. If this is the case, a range of possible ages is given.
Unit: Most fossils are recovered from named geologic formations (e.g. the Morrison Formation or the Hell Creek Formation). When this is not the case, a city or landmark near the locality from which the fossil was recovered is listed.
Material: The vast majority of fossils do not preserve the complete skeleton of an animal. In these cases, the specific bones which are fossilized have been listed.
Notes: Other general information, such as the validity status of the taxon in question, or any other material in the type series may be listed here.
Fossil Research and Development Center, Third Geology and Mineral Resources Exploration Academy of the Gansu Provincial Bureau of Geo-Exploration and Mineral Development
Maiasaura is a large herbivorous saurolophine hadrosaurid ("duck-billed") dinosaur genus that lived in the area currently covered by the state of Montana and the province of Alberta, Canada, in the Upper Cretaceous Period, about 76.7 million years ago. Maiasaura peeblesorum is the state fossil of Montana.
Eolambia is a genus of herbivorous hadrosauroid dinosaur from the early Late Cretaceous of the United States. It contains a single species, E. caroljonesa, named by paleontologist James Kirkland in 1998. The type specimen of Eolambia was discovered by Carole and Ramal Jones in 1993; the species name honors Carole. Since then, hundreds of bones have been discovered from both adults and juveniles, representing nearly every element of the skeleton. All of the specimens have thus far been found in Emery County, Utah, in a layer of rock known as the Mussentuchit Member of the Cedar Mountain Formation.
Anasazisaurus is a genus of saurolophine hadrosaurid ("duckbill") ornithopod dinosaur that lived about 74 million years ago, in the Late Cretaceous Period. It was found in the Farmington Member of the Kirtland Formation, in the San Juan Basin of New Mexico, United States. Only a partial skull has been found to date. It was first described as a specimen of Kritosaurus by Jack Horner, and has been intertwined with Kritosaurus since its description. It is known for its short nasal crest, which stuck out above and between its eyes for a short distance.
Fukuisaurus is a genus of herbivorous ornithopod dinosaur that lived during the Early Cretaceous in what is now Japan. The type species is F. tetoriensis, which was named and described in 2003.
Pararhabdodon is a genus of tsintaosaurin hadrosaurid dinosaur, from the Maastrichtian-age Upper Cretaceous Tremp Group of Spain. The first remains were discovered from the Sant Romà d’Abella fossil locality and assigned to the genus Rhabdodon, and later named as the distinct species Pararhabdodon isonensis in 1993. Known material includes assorted postcranial remains, mostly vertebrae, as well as maxillae from the skull. Specimens from other sites, including remains from France, a maxilla previously considered the distinct taxon Koutalisaurus kohlerorum, an additional maxilla from another locality, the material assigned to the genera Blasisaurus and Arenysaurus, and the extensive Basturs Poble bonebed have been considered at different times to belong to the species, but all of these assignments have more recently been questioned. It was one of the last non-avian dinosaurs known from the fossil record that went extinct during the Cretaceous-Paleogene extinction event.
Lambeosaurini, previously known as Corythosaurini, is one of four tribes of hadrosaurid ornithopods from the family Lambeosaurinae. It is defined as all lambeosaurines closer to Lambeosaurus lambei than to Parasaurolophus walkeri, Tsintaosaurus spinorhinus, or Aralosaurus tuberiferus, which define the other three tribes. Members of this tribe possess a distinctive protruding cranial crest. Lambeosaurins walked the earth for a period of around 12 million years in the Late Cretaceous, though they were confined to regions of modern-day North America and Asia.
Koutalisaurus is a potentially dubious genus of extinct hadrosaurid dinosaur from the Arenysaurini. It is based on a mostly complete dentary from the Maastrichtian-age Upper Cretaceous Tremp Formation near the town of Abella de la Conca, Lleida, Spain.
Velafrons is a genus of lambeosaurine hadrosaurid dinosaur from the Late Cretaceous of Mexico. It is known from a mostly complete skull and partial skeleton of a juvenile individual, with a bony crest on the forehead. Its fossils were found in the late Campanian-age Cerro del Pueblo Formation, near Rincon Colorado, Coahuila, Mexico. The type specimen is CPC-59, and the type species is V. coahuilensis.
The Aguja Formation is a geological formation in North America, exposed in Texas, United States and Chihuahua and Coahuila in Mexico, whose strata date back to the Late Cretaceous. Dinosaur remains are among the fossils that have been recovered from the formation. Fossil palms have also been unearthed here.
The Cerro del Pueblo Formation is a geological formation in Coahuila, Mexico whose strata date back to the Late Cretaceous. Dinosaur remains are among the fossils that have been recovered from the formation. The formation is believed to correlate with the Baculites reesidesi and Baculites jenseni ammonite zones, which dates it to 73.63-72.74 Ma.
Willinakaqe is a dubious genus of saurolophine hadrosaurid dinosaur described based on fossils from the late Cretaceous of the Río Negro Province of southern Argentina.
Magnapaulia is a genus of herbivorous lambeosaurine hadrosaurid dinosaurs known from the Latest Cretaceous Baja California, of northwestern Mexico. It contains a single species, Magnapaulia laticaudus. Magnapaulia was first described in 1981 as a possible species of Lambeosaurus by William J. Morris, and was given its own genus in 2012 by Prieto-Márquez and colleagues.
Tsintaosaurini is a tribe of basal lambeosaurine hadrosaurs native to Eurasia. It is thought to contains the genera Tsintaosaurus, Pararhabdodon and Koutalisaurus, though some studies have questioned its existence as a natural grouping.
Augustynolophus is an extinct genus of herbivorous saurolophine hadrosaur dinosaur which was discovered in the Moreno Formation in California, dating to the late Maastrichtian age, making it one of the last dinosaurs known from the fossil record before the Cretaceous–Paleogene extinction event.
This timeline of hadrosaur research is a chronological listing of events in the history of paleontology focused on the hadrosauroids, a group of herbivorous ornithopod dinosaurs popularly known as the duck-billed dinosaurs. Scientific research on hadrosaurs began in the 1850s, when Joseph Leidy described the genera Thespesius and Trachodon based on scrappy fossils discovered in the western United States. Just two years later he published a description of the much better-preserved remains of an animal from New Jersey that he named Hadrosaurus.
Bonapartesaurus is an extinct genus of herbivorous ornithopod dinosaur belonging to Hadrosauridae, which lived in the area of modern Argentina during the Campanian and Maastrichtian stages of the Late Cretaceous.
David Christopher Evans is a Canadian palaeontologist and evolutionary biologist who specializes in the evolution and paleobiology of Cretaceous dinosaurs in western North America. He received his B.Sc. from the University of British Columbia and his Ph.D. from the University of Toronto. He is a fellow of the Royal Canadian Geographical Society (RCGS) and a member of the Royal Society of Canada and currently serves as the Senior Curator and Temerty Chair of Vertebrate Paleontology at the Royal Ontario Museum in Toronto, Canada. He is also a faculty member in the Department of Ecology & Evolutionary Biology at the University of Toronto. Evans is particularly renowned for his work on the paleobiology of hadrosaur ("duck-billed") dinosaurs and has conducted international research on a wide variety of paleontological topics.
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