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Short description: Extinct clade of dinosaurs

Temporal range:
Early Jurassic–Late Cretaceous, 200.91–66 Ma
(Possible Triassic record)
Ornithischia montage.jpg
A collection of ornithischian fossil skeletons. Clockwise from upper left: Heterodontosaurus (Heterodontosauridae), Nipponosaurus (Ornithopoda), Borealopelta (Ankylosauria), Triceratops (Ceratopsia), Stegoceras (Pachycephalosauria), and Stegosaurus (Stegosauria).
Scientific classification e
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: Ornithischia
Seeley, 1888

Ornithischia (/ˌɔːrnəˈθɪski.ə/) is an extinct clade of mainly herbivorous dinosaurs characterized by a pelvic structure superficially similar to that of birds.[3] The name Ornithischia, or "bird-hipped", reflects this similarity and is derived from the Greek stem ornith- (ὀρνιθ-), meaning "of a bird", and ischion (ἴσχιον), plural ischia, meaning "hip joint". However, birds are only distantly related to this group as birds are theropod dinosaurs.[3] Ornithischians with well known anatomical adaptations include the ceratopsians or "horn-faced" dinosaurs (e.g. Triceratops), the pachycephalosaurs or "thick-headed" dinosaurs, the armored dinosaurs (Thyreophora) such as stegosaurs and ankylosaurs, and the ornithopods.[3] There is strong evidence that certain groups of ornithischians lived in herds,[3][4] often segregated by age group, with juveniles forming their own flocks separate from adults.[5] Some were at least partially covered in filamentous (hair- or feather- like) pelts, and there is much debate over whether these filaments found in specimens of Tianyulong, Psittacosaurus,[6] and Kulindadromeus may have been primitive feathers.[7]


In 1887, Harry Seeley divided Dinosauria into two clades: Ornithischia and Saurischia. Ornithischia is a strongly supported clade with an abundance of diagnostic characters (common traits).[3] The two most notable traits are a "bird-like" hip and beak-like predentary structure, though they shared other features as well.[3]

Early ornithischians were relatively small dinosaurs, averaging about 1–2 meters in body length, with a triangular skull that had large circular orbits on the sides. This suggests that early ornithischians had relatively huge eyes that faced laterally. The forelimbs of early ornithischians are considerably shorter than their hindlimbs. A small forelimb such as those present in early ornithischians would not have been useful for locomotion, and it is evident that early ornithischians were bipedal dinosaurs. The entire skeleton was lightly built, with a largely fenestrated skull and a very stout neck and trunk. The tail is nearly half of the dinosaurs' overall length. The long tail presumably acted as a counterbalance and as a compensating mechanism for shifts in the creature's center of gravity. The hindlimbs of early ornithischians show that the tibia is considerably longer than the femur, a feature that suggests that early ornithischians were adapted for bipedality, and were fast runners.[8]


The ornithischian pelvis was "opisthopubic", meaning that the pubis pointed down and backwards (posterior), parallel with the ischium (Figure 1a).[3] Additionally, the ilium had a forward-pointing process (the preacetabular process) to support the abdomen.[3] This resulted in a four-pronged pelvic structure. In contrast to this, the saurischian pelvis was "propubic", meaning the pubis pointed toward the head (anterior), as in ancestral reptiles (Figure 1b).[3]

The opisthopubic pelvis independently evolved at least three times in dinosaurs (in ornithischians, birds and therizinosauroids).[9] Some argue that the opisthopubic pelvis evolved a fourth time, in the clade Dromaeosauridae, but this is controversial, as other authors argue that dromaeosaurids are mesopubic.[9] It has also been argued that the opisthopubic condition is basal to maniraptorans (including among others birds, therizinosauroids and dromaeosaurids), with some clades having later experienced a reversal to the propubic condition.[10]

Figure 2 - Heterodontosaurus skull with palpebral bone (colored red), antorbital fenestra (yellow) and predentary (green).[3]


Ornithischians shared a unique bone called the predentary (Figure 2).[3] This unpaired bone was situated at the front of the lower jaw, where it extended the dentary (the main lower jaw bone). The predentary coincided with the premaxilla in the upper jaw. Together, they formed a beak-like apparatus used to clip off plant material. In ceratopsian dinosaurs, it opposed the rostral bone.[citation needed]

In 2017 Baron & Barrett suggested that Chilesaurus may represent an early diverging ornithischian that had not yet acquired the predentary of all other ornithischians.[11]

Other characteristics

  • Ornithischians had paired premaxillary bones that were toothless and roughened at the tip of the snout (presumably due to the attachment of a keratinous beak).[3]
  • Ornithischians developed a narrow "eyebrow", or palpebral bone, across the outside of the eye socket.[3]
  • Ornithischians had reduced, or even closed-off, antorbital fenestrae (the fenestra in front of the eye socket).[3]
  • Ornithischian jaw joints were lowered below the level of the teeth, bringing the teeth into simultaneous occlusion.[3]
  • Ornithischians had "leaf-shaped" cheek teeth.[3]
  • Ornithischian backbones were stiffened near the pelvis by the ossification of tendons above the sacrum. Additionally, ornithischians had at least five sacral vertebrae attaching to the pelvis.[3]


Ornithischia is a branch-based clade defined as all dinosaurs more closely related to Iguanodon than to either Allosaurus or Camarasaurus.[1]

During its long history of study, numerous different subgroups of ornithischians have been recognized. Since the 1980s, many have been given phylogenetic definitions in accordance to the International Code of Zoological Nomenclature (ICZN). In 2020, the International Code of Phylogenetic Nomenclature (also known as the ICPN or PhyloCode) was formalized, which treats all the definitions made under the ICZN as informal and inapplicable for scientific use unless re-registered under the ICPN. In 2021, an international group of researchers led by Daniel Madzia registered almost all of the most commonly used ornithischian clades under the ICPN, with the intent of standardizing their definitions. A composite cladogram showing most of their clades and specifiers is shown below.[1]

Due to the complexities of early ornithischian evolution, Madzia and colleagues named the new clade Saphornithischia to encompass the taxa traditionally considered ornithischians, to the exclusion of potentially early forms like Silesauridae, Pisanosaurus or Chilesaurus, which some authors have considered basal ornithischians while others consider them non-ornithischians or non-dinosaurs.[1]

In 2022, Norman et al. redefined the clade Prionodontia, proposed by Richard Owen in 1874 and often seen as a synonym of Ornithischia, to be the least inclusive clade including Iguanodon, Scelidosaurus, and Echinodon, similar to its original proposal. They note that it would represent the same clade as Saphornithischia, and despite the latter being registered under the ICPN, Prionodontia may receive priority as it was coined over a century earlier. Their analysis also treats "silesaurids" as a paraphyletic grade of basal ornithischians forming no distinct family, so they coin the clade Parapredentata to include all dinosaurs in the least inclusive clade containing Silesaurus and Iguanodon.[12]

Allosaurus (Theropoda)

Camarasaurus (Sauropodomorpha)


Heterodontosaurus tucki (Heterodontosauridae) Heterodontosaurus restoration.jpg


Huayangosaurus taibaii (Huayangosauridae)

Stegosaurus stenops (Stegosauridae) Stegosaurus stenops sophie wiki martyniuk.png


Mymoorapelta maysi


Polacanthus foxii (Polacanthinae) Polacanthus foxii.jpg


Nodosaurus textilis

Panoplosaurus mirus (Panoplosaurini)

Struthiosaurus austriacus (Struthiosaurini)


Hylaeosaurus armatus


Gobisaurus domoculus

Shamosaurus scutatus


Pinacosaurus grangeri

Saichania chulsanensis

Ankylosaurus magniventris (Ankylosaurini) Ankylosaurus magniventris reconstruction.png


Jeholosaurus shangyuanensis (Jeholosauridae)


Orodromeus makelai (Orodrominae)

Thescelosaurus neglectus (Thescelosaurinae)

Hypsilophodon foxii (Hypsilophodontidae) Hypsilophodon.jpg


Stegoceras validum Stegoceras validum.jpg


Sphaerotholus goodwini

Pachycephalosaurus wyomingensis (Pachycephalosaurini)


Psittacosaurus mongoliensis

Chaoyangsaurus youngi (Chaoyangsauridae)


Leptoceratops gracilis (Leptoceratopsidae)


Protoceratops andrewsi (Protoceratopsidae) Protoceratops reconstruction.png


Ceratops montanus


Chasmosaurus belli

Anchiceratops ornatus
Anchiceratops dinosaur.png

Arrhinoceratops brachyops

Triceratops horridus (Triceratopsini)


Nasutoceratops titusi (Nasutoceratopsini)

Centrosaurus apertus (Centrosaurini)

Achelousaurus horneri

Pachyrhinosaurus canadensis


Gasparinisaura cincosaltensis Gasparinisaura BW.jpg

Macrogryphosaurus gondwanicus

Talenkauen santacrucensis


Rhabdodon priscus

Zalmoxes robustus

Tenontosaurus tilletti Tenontosaurus BW.jpg


Dryosaurus altus (Dryosauridae)


Camptosaurus dispar (Camptosauridae) Camptosaurus.jpg


Hypselospinus fittoni


Iguanodon bernissartensis (Iguanodontidae) Iguanodon NT.jpg


Probactrosaurus gobiensis


Hadrosaurus foulkii (Hadrosaurinae)

Saurolophus osborni (Saurolophinae) Saurolophus scalation.png

Lambeosaurus lambei (Lambeosaurinae)


As of the late 2010s, the exact placement of Ornithischia within the dinosaur lineage is a contentious issue.[13] Traditionally, Ornithischia is considered the sister group of Saurischia (which contains Theropoda and Sauropodomorpha).[14] However, in the alternative hypothesis of dinosaur relationships that was proposed by Baron, Norman & Barrett in the journal Nature in 2017, Ornithischia was recovered as the sister group to the Theropoda, which grouped together in the clade Ornithoscelida.[15][16] This hypothesis was recently challenged by an international consortium of early dinosaur experts led by Max Langer. However, the data that supported the more traditional placement of Ornithischia, as sister taxon of Saurischia, was found not to be statistically significant from the evidence that supported the Ornithoscelida hypothesis, in both the study by Langer et al. and the reply to the study by Baron et al.[17][18] A further 2017 study found some support for the previously abandoned Phytodinosauria model, which classifies ornithischians together with sauropodomorphs.[19]


Ornithischians shifted from bipedal to quadrupedal posture at least three times in their evolutionary history and it has been shown primitive members may have been capable of both forms of movement.[20]

Most ornithischians were herbivorous.[3] In fact, most of the unifying characters of Ornithischia are thought to be related to this herbivory.[3] For example, the shift to an opisthopubic pelvis is thought to be related to the development of a large stomach or stomachs and gut which would allow ornithischians to more effectively digest plant matter.[3] The smallest known ornithischian is Fruitadens haagarorum.[21] The largest Fruitadens individuals reached just 65–75 cm. Previously, only carnivorous, saurischian theropods were known to reach such small sizes.[21] At the other end of the spectrum, the largest known ornithischians reach about 15 meters (smaller than the largest saurischians).[22]

However, not all ornithischians were strictly herbivorous. Some groups, like the heterodontosaurids, were likely omnivores.[23] At least one species of ankylosaurian, Liaoningosaurus paradoxus, appears to have been at least partially carnivorous, with hooked claws, fork-like teeth, and stomach contents suggesting that it may have fed on fish.[24]

There is strong evidence that some ornithischians lived in herds.[3][4] This evidence consists of multiple bone beds where large numbers of individuals of the same species and of different age groups died simultaneously.[3][4]

See also


  1. 1.0 1.1 1.2 1.3 1.4 Madzia, D.; Arbour, V.M.; Boyd, C.A.; Farke, A.A.; Cruzado-Caballero, P.; Evans, D.C. (2021). "The phylogenetic nomenclature of ornithischian dinosaurs". PeerJ 9: e12362. doi:10.7717/peerj.12362. PMID 34966571. 
  2. Ferigolo, J.; Langer, M. C. (2007). "A Late Triassic dinosauriform from south Brazil and the origin of the ornithischian predentary bone". Historical Biology 19: 23–33. doi:10.1080/08912960600845767. 
  3. 3.00 3.01 3.02 3.03 3.04 3.05 3.06 3.07 3.08 3.09 3.10 3.11 3.12 3.13 3.14 3.15 3.16 3.17 3.18 3.19 3.20 3.21 3.22 3.23 Fastovsky, David E.; Weishampel, David B. (2012). Dinosaurs: A Concise Natural History. Cambridge: Cambridge University Press. ISBN 978-1107276468. 
  4. 4.0 4.1 4.2 Qi, Zhao; Barrett, Paul M.; Eberth, David A. (2007-09-01). "Social Behaviour and Mass Mortality in the Basal Ceratopsian Dinosaur Psittacosaurus (early Cretaceous, People's Republic of China)" (in en). Palaeontology 50 (5): 1023–1029. doi:10.1111/j.1475-4983.2007.00709.x. ISSN 1475-4983. Bibcode2007Palgy..50.1023Q. 
  5. Zhao, Q. (2013). "Juvenile-only clusters and behaviour of the Early Cretaceous dinosaur Psittacosaurus". Acta Palaeontologica Polonica. doi:10.4202/app.2012.0128. 
  6. Mayr, Gerald; Peters, Stefan D.; Plodowski, Gerhard; Vogel, Olaf (2002-08-01). "Bristle-like integumentary structures at the tail of the horned dinosaur Psittacosaurus" (in en). Naturwissenschaften 89 (8): 361–365. doi:10.1007/s00114-002-0339-6. ISSN 0028-1042. PMID 12435037. Bibcode2002NW.....89..361M. 
  7. Godefroit, P.; Sinitsa, S.M.; Dhouailly, D.; Bolotsky, Y.L.; Sizov, A.V.; McNamara, M.E.; Benton, M.J.; Spagna, P. (2014). "A Jurassic ornithischian dinosaur from Siberia with both feathers and scales". Science 345 (6195): 451–455. doi:10.1126/science.1253351. PMID 25061209. Bibcode2014Sci...345..451G. Retrieved 2016-08-28. 
  8. Colbert, E. H. (1981). A primitive ornithischian dinosaur from the Kayenta Formation of Arizona. Museum Northern Arizona Bull. 53, 1-61
  9. 9.0 9.1 Currie, Philip J.; Padian, Kevin (1997-10-06) (in en). Encyclopedia of Dinosaurs. Academic Press. pp. 537–538. ISBN 9780080494746. 
  10. Holtz, T.R. and Osmólska, H. (2004). "Saurischia." In Weishampel, Dodson and Osmólska (eds.), The Dinosauria, second edition. Berkeley: University of California Press.
  11. Baron, Matthew G.; Barrett, Paul M. (2017). "A dinosaur missing-link? Chilesaurus and the early evolution of ornithischian dinosaurs". Biology Letters 13 (8): 20170220. doi:10.1098/rsbl.2017.0220. PMID 28814574. 
  12. "Taxonomic, palaeobiological and evolutionary implications of a phylogenetic hypothesis for Ornithischia (Archosauria: Dinosauria)". Zoological Journal of the Linnean Society 196 (4): 1273–1309. 2022. doi:10.1093/zoolinnean/zlac062. 
  13. Matthew G. Baron (2018). "Pisanosaurus mertii and the Triassic ornithischian crisis: could phylogeny offer a solution?". Historical Biology: An International Journal of Paleobiology 31 (8): 967–981. doi:10.1080/08912963.2017.1410705. 
  14. Seeley, H.G. (1888). "On the classification of the fossil animals commonly named Dinosauria". Proceedings of the Royal Society of London 43 (258–265): 165–171. doi:10.1098/rspl.1887.0117. 
  15. Baron, M.G.; Norman, D.B.; Barrett, P.M. (2017). "A new hypothesis of dinosaur relationships and early dinosaur evolution". Nature 543 (7646): 501–506. doi:10.1038/nature21700. PMID 28332513. Bibcode2017Natur.543..501B. 
  16. "New study shakes the roots of the dinosaur family tree". 2017-03-22. 
  17. Max C. Langer; Martín D. Ezcurra; Oliver W. M. Rauhut; Michael J. Benton; Fabien Knoll; Blair W. McPhee; Fernando E. Novas; Diego Pol et al. (2017). "Untangling the dinosaur family tree". Nature 551 (7678): E1–E3. doi:10.1038/nature24011. PMID 29094688. Bibcode2017Natur.551E...1L. 
  18. Matthew G. Baron; David B. Norman; Paul M. Barrett (2017). "Baron et al. reply". Nature 551 (7678): E4–E5. doi:10.1038/nature24012. PMID 29094705. Bibcode2017Natur.551E...4B. 
  19. Luke A. Parry; Matthew G. Baron; Jakob Vinther (2017). "Multiple optimality criteria support Ornithoscelida". Royal Society Open Science 4 (10): 170833. doi:10.1098/rsos.170833. PMID 29134086. Bibcode2017RSOS....470833P. 
  20. Jeffrey A. Wilson; Claudia A. Marsicano; Roger M. H. Smith (6 October 2009). "Dynamic Locomotor Capabilities Revealed by Early Dinosaur Trackmakers from Southern Africa". PLOS ONE 4 (10): e7331. doi:10.1371/journal.pone.0007331. PMID 19806213. Bibcode2009PLoSO...4.7331W. 
  21. 21.0 21.1 Butler, Richard J.; Galton, Peter M.; Porro, Laura B.; Chiappe, Luis M.; Henderson, Donald M.; Erickson, Gregory M. (2010-02-07). "Lower limits of ornithischian dinosaur body size inferred from a new Upper Jurassic heterodontosaurid from North America" (in en). Proceedings of the Royal Society of London B: Biological Sciences 277 (1680): 375–381. doi:10.1098/rspb.2009.1494. ISSN 0962-8452. PMID 19846460. 
  22. Yannan, Ji; Xuri, Wang; Yongqing, Liu; Qiang, Ji (2011-02-01). "Systematics, Behavior and Living Environment of Shantungosaurus Giganteus (Dinosauria: Hadrosauridae)" (in en). Acta Geologica Sinica - English Edition 85 (1): 58–65. doi:10.1111/j.1755-6724.2011.00378.x. ISSN 1755-6724. 
  23. Barrett, P. M.; Rayfield, E. J. (2006). "Ecological and evolutionary implications of dinosaur feeding behaviour". Trends in Ecology & Evolution 21 (4): 217–224. doi:10.1016/j.tree.2006.01.002. PMID 16701088. 
  24. Ji, Q.; Wu, X.; Cheng, Y.; Ten, F.; Wang, X.; Ji, Y. (2016). "Fish-hunting ankylosaurs (Dinosauria, Ornithischia) from the Cretaceous of China". Journal of Geology 40: 2. 
  • Butler, R.J. (2005). "The 'fabrosaurid' ornithischian dinosaurs of the Upper Elliot formation (lower Jurassic) of South Africa and Lesotho". Zoological Journal of the Linnean Society 145 (2): 175–218. doi:10.1111/j.1096-3642.2005.00182.x. 
  • Sereno, P.C. (1986). "Phylogeny of the bird-hipped dinosaurs (order Ornithischia)". National Geographic Research 2 (2): 234–256. 

External links

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