List of Asian dinosaurs
This is a list of dinosaurs whose remains have been recovered from Asia, excluding India, which was part of a separate landmass for much of the Mesozoic (See List of Indian and Madagascan Dinosaurs for a list of Dinosaurs from India). This list does not include dinosaurs that live or lived after the Mesozoic era such as birds.
Criteria for inclusion
[edit]- The genus must appear on the List of dinosaur genera.
- At least one named species of the creature must have been found in Asia.
- This list is a complement to Category:Mesozoic dinosaurs of Asia.
List of Asian dinosaurs
[edit]Valid genera
[edit]Name | Year | Formation | Location | Notes | Images |
---|---|---|---|---|---|
Abdarainurus | 2020 | Alagteeg Formation (Late Cretaceous, Santonian to Campanian) | ![]() | Inconsistent in phylogenetic placement; could represent an unknown lineage of macronarians[1] | ![]() |
Abrosaurus | 1989 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | ![]() | Had unusually large fenestrae | ![]() |
Achillobator | 1999 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | ![]() | Its robust build suggests it was not a cursorial animal[2] | ![]() |
Adasaurus | 1983 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Its sickle claw was markedly reduced compared to other dromaeosaurids | ![]() |
Aepyornithomimus | 2017 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | The first ornithomimosaur named from a dry desert environment | ![]() |
Agilisaurus | 1990 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | ![]() | The holotype specimen was discovered during the construction of the museum where it is now housed | ![]() |
Albalophosaurus | 2009 | Kuwajima Formation (Early Cretaceous, Valanginian to Hauterivian) | ![]() | Only known from fragments of a skull | ![]() |
Albinykus | 2011 | Javkhlant Formation (Late Cretaceous, Santonian) | ![]() | Preserved in a sitting position not unlike that of modern birds | ![]() |
Alectrosaurus | 1933 | Iren Dabasu Formation (Late Cretaceous, Cenomanian to Santonian) | ![]() | Had long legs which may be an adaptation to pursuit predation[3] | ![]() |
Alioramus | 1976 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Possessed an elongated snout with a row of short crests | ![]() |
Almas | 2017 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | Preserved alongside eggshells which may have come from a troodontid[4] | ![]() |
Altirhinus | 1998 | Khuren Dukh Formation (Early Cretaceous, Barremian to Albian) | ![]() | Had a distinctive, elevated nasal bone which supported a large nasal cavity | |
Alxasaurus | 1993 | Bayin-Gobi Formation (Early Cretaceous, Albian) | ![]() | Most of the skeleton is known, which allowed researchers to connect therizinosaurs to other theropods | |
Ambopteryx | 2019 | Unnamed formation (Late Jurassic, Oxfordian) | ![]() | Preserves stomach contents containing gastroliths and fragments of bone, suggesting an omnivorous diet | ![]() |
Amtocephale | 2011 | Bayan Shireh Formation (Late Cretaceous, Turonian to Santonian) | ![]() | One of the oldest known pachycephalosaurs | ![]() |
Amurosaurus | 1991 | Udurchukan Formation (Late Cretaceous, Maastrichtian) | ![]() | One specimen may have come from an individual with a limp[5] | ![]() |
Analong | 2020 | Chuanjie Formation (Middle Jurassic, Bajocian) | ![]() | Originally described as a specimen of Chuanjiesaurus but assigned a new genus due to several morphological differences | |
Anchiornis | 2009 | Tiaojishan Formation (Late Jurassic, Oxfordian) | ![]() | Analysis of fossilized melanosomes suggest a mostly gray or black body, white and black patterns on its wings, and a red head crest[6] | ![]() |
Anhuilong | 2020 | Hongqin Formation (Middle Jurassic, Aalenian to Callovian) | ![]() | Closely related to Huangshanlong and Omeisaurus, all forming an exclusive clade of mamenchisaurids | ![]() |
Anomalipes | 2018 | Wangshi Group (Late Cretaceous, Maastrichtian) | ![]() | May have been closely related to Gigantoraptor despite its significantly smaller size[7] | ![]() |
Anserimimus | 1988 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Had powerful forelimbs with uniquely straight, flattened claws | ![]() |
Aorun | 2013 | Shishugou Formation, (Late Jurassic, Oxfordian) | ![]() | Potentially a basal member of the alvarezsaurian lineage[8] | ![]() |
Aralosaurus | 1968 | Bostobe Formation, (Late Cretaceous, Santonian to Campanian) | ![]() | Its crest has been interpreted as being arch-shaped as in kritosaurin hadrosaurs, but this cannot be confirmed | ![]() |
Archaeoceratops | 1997 | Xinminbao Group (Early Cretaceous, Barremian) | ![]() | Had no horns and only the beginnings of a frill | ![]() |
Archaeornithoides | 1992 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | Known from only a partial skull with scratches that may have been created by a small mammal[9] | ![]() |
Archaeornithomimus | 1972 | Bissekty Formation?, Iren Dabasu Formation (Late Cretaceous, Cenomanian to Turonian) | ![]() ![]() | Unlike other ornithomimosaurs, its feet were not arctometatarsalian | ![]() |
Arkharavia | 2010 | Udurchukan Formation (Late Cretaceous, Maastrichtian) | ![]() | Described from a series of vertebrae, several of which were found to not belong to this taxon[10] | ![]() |
Arstanosaurus | 1982 | Bostobe Formation (Late Cretaceous, Santonian to Campanian) | ![]() | Poorly known | |
Asiaceratops | 1989 | Khodzhakul Formation, Xinminbao Group? (Late Cretaceous, Cenomanian) | ![]() ![]() | Potentially a leptoceratopsid[11] | |
Asiatosaurus | 1924 | Öösh Formation, Xinlong Formation (Early Cretaceous, Barremian to Albian) | ![]() ![]() | Two species have been named but both are only known from extremely scant remains | ![]() |
Auroraceratops | 2005 | Xinminbao Group (Early Cretaceous, Aptian) | ![]() | Known from more than eighty specimens, including complete skeletons | ![]() |
Aurornis | 2013 | Tiaojishan Formation (Late Jurassic, Oxfordian) | ![]() | If an avialan as originally described it would be one of the oldest members of the group | ![]() |
Avimimus | 1981 | Barun Goyot Formation, Nemegt Formation (Late Cretaceous, Campanian to Maastrichtian) | ![]() | Bonebed remains indicate a gregarious lifestyle; it may have formed age-segregated herds for lekking or flocking purposes[12] | ![]() |
Bactrosaurus | 1933 | Iren Dabasu Formation, Majiacun Formation? (Late Cretaceous, Cenomanian to Santonian?) | ![]() | Remains of at least six individuals are known, making up much of the skeleton | ![]() |
Bagaceratops | 1975 | Barun Goyot Formation, Bayan Mandahu Formation, Djadochta Formation? (Late Cretaceous, Campanian to Maastrichtian) | ![]() ![]() | May have been a direct descendant of Protoceratops which it physically resembles[13] | ![]() |
Bagaraatan | 1996 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Combines traits of several theropod groups, possibly due to being chimaeric[14] | ![]() |
Bainoceratops | 2003 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | Its supposedly diagnostic features may fall within Protoceratops variation[15] | |
Banji | 2010 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | ![]() | Vertical striations adorned the sides of its crest | ![]() |
Bannykus | 2018 | Bayin-Gobi Formation (Early Cretaceous, Barremian to Aptian) | ![]() | Exhibited a transitional hand morphology for an alvarezsaur, having three fingers of roughly equal length with the first being robust | ![]() |
Baotianmansaurus | 2009 | Gaogou Formation (Late Cretaceous, Cenomanian to Turonian) | ![]() | Large but known from only a few bones | ![]() |
Barsboldia | 1981 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Possessed elongated neural spines particularly above the hips | ![]() |
Bashanosaurus | 2022 | Shaximiao Formation (Middle Jurassic, Bajocian) | ![]() | Its skeleton combines traits of stegosaurs and more basal thyreophorans | |
Bashunosaurus | 2004 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | ![]() | Although described as a macronarian, this has yet to be rigorously tested[16] | |
Batyrosaurus | 2012 | Bostobe Formation (Late Cretaceous, Santonian to Campanian) | ![]() | Remains originally identified as Arstanosaurus | ![]() |
Bayannurosaurus | 2018 | Bayin-Gobi Formation (Early Cretaceous, Aptian) | ![]() | Known from a well-preserved, almost complete skeleton | ![]() |
Beg | 2020 | Ulaanoosh Formation (Early Cretaceous to Late Cretaceous, Albian to Cenomanian) | ![]() | Its preserved skull has a rugose texture | ![]() |
Beibeilong | 2017 | Gaogou Formation (Late Cretaceous, Cenomanian to Coniacian) | ![]() | Similar to but more basal than Gigantoraptor.[17] Known from only a single embryo still in its egg | ![]() |
Beipiaosaurus | 1999 | Yixian Formation (Early Cretaceous, Aptian) | ![]() | Preserves evidence of downy feathers as well as a secondary coat of simpler "elongated broad filamentous feathers" or EBFFs[18] | ![]() |
Beishanlong | 2010 | Xinminbao Group (Early Cretaceous, Aptian to Albian) | ![]() | Lacked the elongated claws of more derived ornithomimosaurs | ![]() |
Bellusaurus | 1990 | Shishugou Formation (Late Jurassic, Oxfordian) | ![]() | Known from a bone bed with the remains of seventeen juvenile specimens | ![]() |
Bienosaurus | 2001 | Lufeng Formation (Early Jurassic, Sinemurian) | ![]() | Potentially synonymous with Tatisaurus[19] | ![]() |
Bissektipelta | 2004 | Bissekty Formation (Late Cretaceous, Turonian to Coniacian) | ![]() | Analysis of its braincase suggests poor hearing and eyesight but good olfaction and taste; it has been suggested to be a filter feeder[20] | |
Bolong | 2010 | Yixian Formation (Early Cretaceous, Aptian) | ![]() | Originally known from only a skull; an almost complete skeleton was described in 2013[21] | ![]() |
Borealosaurus | 2004 | Sunjiawan Formation (Late Cretaceous, Cenomanian to Turonian) | ![]() | Its caudal vertebrae were distinctively opisthocoelous | |
Borogovia | 1987 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Had a uniquely straight and flattened sickle claw, which may have had a weight-bearing function | ![]() |
Breviceratops | 1990 | Barun Goyot Formation (Late Cretaceous, Campanian) | ![]() | Only known from juvenile remains but can be distinguished from other protoceratopsids | ![]() |
Brohisaurus | 2003 | Sembar Formation (Late Jurassic, Kimmeridgian) | ![]() | Possibly an early titanosauriform | |
Byronosaurus | 2000 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | Two juvenile skulls were found in an oviraptorid nest and claimed to be evidence for nest parasitism in this taxon, but both their identity and taphonomy have been questioned[4][22] | ![]() |
Caenagnathasia | 1994 | Bissekty Formation (Late Cretaceous, Turonian to Coniacian) | ![]() | One of the oldest and smallest known caenagnathoids | ![]() |
Caihong | 2018 | Tiaojishan Formation (Late Jurassic, Oxfordian) | ![]() | Possessed platelet-shaped melanosomes that produced iridesence as in modern trumpeters | ![]() |
Caudipteryx | 1998 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | Two species are known. At least C. zoui did not have secondary feathers attached to the lower arm | |
Ceratonykus | 2009 | Barun Goyot Formation (Late Cretaceous, Campanian) | ![]() | Several osteological features were described as similar to ornithischians[23] | ![]() |
Changchunsaurus | 2005 | Quantou Formation (Early Cretaceous to Late Cretaceous, Aptian to Cenomanian) | ![]() | Had wavy enamel on its leaf-shaped teeth that made them more resistant to wear; this feature is also present in hadrosaurs[24] | ![]() |
Changmiania | 2020 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | Preserved in a curled-up position as if sleeping in a potential burrow | ![]() |
Changyuraptor | 2014 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | The largest microraptorian dromaeosaurid known. Had tail feathers almost a foot long[25] | ![]() |
Chaoyangsaurus | 1999 | Tuchengzi Formation (Late Jurassic, Tithonian) | ![]() | Known by a number of alternate spellings (e.g. Chaoyangosaurus, Chaoyoungosaurus) before its formal description | ![]() |
Charonosaurus | 2000 | Yuliangze Formation (Late Cretaceous, Maastrichtian) | ![]() | May have had a long, backwards-arcing crest similar to that of Parasaurolophus | ![]() |
Chialingosaurus | 1959 | Shaximiao Formation (Late Jurassic, Oxfordian to Kimmeridgian) | ![]() | Had both large plates and smaller spines, similar to Kentrosaurus | ![]() |
Chiayusaurus | 1953 | Hasandong Formation, Xinminbao Group (Early Cretaceous, Barremian to Albian) | ![]() ![]() | Two species have been named, both from teeth. Those of C. lacustris are apparently indistinguishable to those of Euhelopus[26] or Mamenchisaurus[27] | |
Chilantaisaurus | 1964 | Ulansuhai Formation (Late Cretaceous, Turonian) | ![]() | Had a particularly hooked claw on its first finger | ![]() |
Chingkankousaurus | 1958 | Wangshi Group (Late Cretaceous, Santonian to Campanian) | ![]() | Known from only a scapula. Possibly a tyrannosauroid[28] | |
Chinshakiangosaurus | 1992 | Fengjiahe Formation (Early Jurassic, Hettangian) | ![]() | Had a U-shaped snout that may have supported fleshy cheeks, an adaptation to bulk feeding | |
Choyrodon | 2018 | Khuren Dukh Formation (Early Cretaceous, Albian) | ![]() | It had an enlarged nose similar to its contemporary, Altirhinus, but it is most likely a separate taxon[29] | ![]() |
Chuandongocoelurus | 1984 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | ![]() | A tetanuran of uncertain relationships | ![]() |
Chuanjiesaurus | 2000 | Chuanjie Formation (Middle Jurassic, Bathonian) | ![]() | One of the more derived mamenchisaurids[30] | ![]() |
Chuanqilong | 2014 | Jiufotang Formation (Early Cretaceous, Barremian to Aptian) | ![]() | May have been the adult form of the coeval Liaoningosaurus[31] | ![]() |
Chungkingosaurus | 1983 | Shaximiao Formation (Late Jurassic, Oxfordian) | ![]() | May have possessed at least six thagomizer spikes; the rearmost pair was mounted horizontally, directed outwards and backwards | ![]() |
Chuxiongosaurus | 2010 | Lufeng Formation (Early Jurassic, Hettangian to Pliensbachian) | ![]() | Potentially a synonym of Jingshanosaurus[32] | |
Citipati | 2001 | Djadochta Formation (Late Cretaceous, Campanian to Maastrichtian) | ![]() | Had a distinctive triangular crest. A referred specimen known as the Zamyn Khondt oviraptorid possessed the familiar rectangular domed crest in most depictions of Oviraptor, but likely does not belong to that genus or Citipati[33] | ![]() |
Conchoraptor | 1986 | Barun Goyot Formation, Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Named for a hypothesized diet of shellfish, but this cannot be confirmed | ![]() |
Corythoraptor | 2017 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | ![]() | Its crest was vertical and rectangular, not unlike that of a cassowary | ![]() |
Crichtonpelta | 2015 | Sunjiawan Formation (Late Cretaceous, Cenomanian) | ![]() | Originally named as a second species of Crichtonsaurus | |
Crichtonsaurus | 2002 | Sunjiawan Formation (Late Cretaceous, Cenomanian to Turonian) | ![]() | Sometimes reconstructed with semicircular osteoderms vaguely similar to the plates of stegosaurs | ![]() |
Daanosaurus | 2005 | Shaximiao Formation (Late Jurassic, Oxfordian to Tithonian) | ![]() | Phylogenetic position is uncertain as it is only known from the remains of a juvenile | |
Daliansaurus | 2017 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | Had an enlarged claw on the fourth toe comparable in size to the sickle claw on its second | ![]() |
Dashanpusaurus | 2005 | Shaximiao Formation (Middle Jurassic, Callovian) | ![]() | One of the basalmost and earliest known macronarians[34] | |
Datanglong | 2014 | Xinlong Formation (Early Cretaceous, Barremian to Albian) | ![]() | Had a uniquely pneumatized ilium similar to megaraptorans | |
Datonglong | 2016 | Huiquanpu Formation (Late Cretaceous, Cenomanian to Campanian) | ![]() | Precise dating uncertain | |
Datousaurus | 1984 | Shaximiao Formation (Middle Jurassic to Late Jurassic, Bathonian to Oxfordian) | ![]() | One of the rarer sauropods of the Shaximiao, known from only two skeletons and a large, deep skull | ![]() |
Daurlong | 2022 | Longjiang Formation (Early Cretaceous, Aptian) | ![]() | Preserves remains of an intestinal tract | ![]() |
Daxiatitan | 2008 | Hekou Group (Early Cretaceous, Barremian) | ![]() | Large and very long-necked | ![]() |
Deinocheirus | 1970 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Had a suite of unique features, most notably a hump supported by elongated neural spines | ![]() |
Dilong | 2004 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | Preserves evidence of a coating of simple feathers | ![]() |
Dongbeititan | 2007 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | A theropod tooth has been found encrusted in one of its ribs[35] | ![]() |
Dongyangopelta | 2013 | Chaochuan Formation (Early Cretaceous to Late Cretaceous, Albian to Cenomanian) | ![]() | Coexisted with Zhejiangosaurus but could be distinguished based on subtle osteological features[36] | |
Dongyangosaurus | 2008 | Jinhua Formation (Late Cretaceous, Turonian to Coniacian) | ![]() | Its phylogenetic placement is uncertain | ![]() |
Dzharaonyx | 2022 | Bissekty Formation (Late Cretaceous, Turonian) | ![]() | One of the oldest known parvicursorines | |
Dzharatitanis | 2021 | Bissekty Formation (Late Cretaceous, Turonian) | ![]() | Originally described as a rebbachisaurid[37] but later reinterpreted as a titanosaur with possible lognkosaurian affinities[38] | ![]() |
Elmisaurus | 1981 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | One of the most complete caenagnathids known | ![]() |
Embasaurus | 1931 | Neocomian Sands (Early Cretaceous, Berriasian) | ![]() | Known from only two vertebrae | ![]() |
Enigmosaurus | 1983 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | ![]() | Had a large, backwards-pointing pelvis | ![]() |
Eomamenchisaurus | 2008 | Zhanghe Formation (Middle Jurassic to Late Jurassic, Aalenian to Oxfordian) | ![]() | One of the oldest mamenchisaurids | |
Eosinopteryx | 2013 | Tiaojishan Formation (Late Jurassic, Oxfordian) | ![]() | Described as lacking advanced tail feathers and long "hind wings", unlike other paravians, but this may be an artifact of preservation[39] | ![]() |
Epidexipteryx | 2008 | Haifanggou Formation (Middle Jurassic, Callovian) | ![]() | Supported four long feathers from an abbreviated tail | ![]() |
Equijubus | 2003 | Xinminbao Group (Early Cretaceous, Albian) | ![]() | A grazer that preserves the oldest known evidence of grass-eating[40] | ![]() |
Erketu | 2006 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | ![]() | May have had the longest neck of any dinosaur relative to its body | ![]() |
Erliansaurus | 2002 | Iren Dabasu Formation (Late Cretaceous, Cenomanian) | ![]() | Had long, curved claws on its fingers | ![]() |
Erlikosaurus | 1980 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | ![]() | Preserves the most complete skull known from any therizinosaur | ![]() |
Eshanosaurus | 2001 | Lufeng Formation (Early Jurassic, Hettangian) | ![]() | Has been suggested to be the oldest known therizinosaur | ![]() |
Euhelopus | 1956 | Meng-Yin Formation (Early Cretaceous, Berriasian to Valanginian) | ![]() | Originally believed to have lived in a marshy environment | ![]() |
Euronychodon | 1991 | Bissekty Formation (Late Cretaceous, Turonian) | ![]() | Type species was found in Portugal. The Asian species may represent a form taxon of improperly developed teeth[41] | |
Ferganasaurus | 2003 | Balabansai Formation (Middle Jurassic, Callovian) | ![]() | Claimed to have two hand claws, but this is disputed[42] | |
Ferganocephale | 2005 | Balabansai Formation (Middle Jurassic, Callovian) | ![]() | Unusually, its teeth were not serrated | |
Fujianvenator | 2023 | Nanyuan Formation (Late Jurassic, Tithonian) | ![]() | Possessed proportionally long legs which may be an adaptation to wading | ![]() |
Fukuiraptor | 2000 | Kitadani Formation, Sebayashi Formation? (Early Cretaceous, Barremian to Aptian) | ![]() | Similarly to Megaraptor, it was originally reconstructed as a dromaeosaur with its hand claw on its foot | ![]() |
Fukuisaurus | 2003 | Kitadani Formation (Early Cretaceous, Barremian) | ![]() | The elements of its skull are so strongly fused that it was unable to chew[43] | ![]() |
Fukuititan | 2010 | Kitadani Formation (Early Cretaceous, Barremian to Aptian) | ![]() | The first sauropod named from Japan | ![]() |
Fukuivenator | 2016 | Kitadani Formation (Early Cretaceous, Barremian to Aptian) | ![]() | Possesses traits of various groups of coelurosaurs, though probably a therizinosaur.[44] May have been a herbivore or omnivore due to its heterodont dentition | ![]() |
Fulengia | 1977 | Lufeng Formation (Early Jurassic, Hettangian to Toarcian) | ![]() | May have been a juvenile Lufengosaurus | |
Fushanosaurus | 2019 | Shishugou Formation (Late Jurassic, Oxfordian) | ![]() | Known from a single femur of immense size | |
Fusuisaurus | 2006 | Xinlong Formation (Early Cretaceous, Aptian to Albian) | ![]() | A referred humerus may support an extremely large size for this taxon[45] | |
Gallimimus | 1972 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Had a relatively long beak with a rounded tip | ![]() |
Gannansaurus | 2013 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | ![]() | Its vertebrae were more similar to those of Euhelopus than to other sauropods | ![]() |
Ganzhousaurus | 2013 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | ![]() | Coexisted with at least seven other oviraptorosaurs, which may have niche-partitioned. It was likely primarily herbivorous[46] | ![]() |
Garudimimus | 1981 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | ![]() | Was not as well-adapted to running as later ornithomimosaurs | ![]() |
Gasosaurus | 1985 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | ![]() | Discovered as a byproduct of construction work | ![]() |
Gigantoraptor | 2007 | Iren Dabasu Formation (Late Cretaceous, Cenomanian) | ![]() | The largest known oviraptorosaur, comparable in size to Albertosaurus | ![]() |
Gigantspinosaurus | 1992 | Shaximiao Formation (Late Jurassic, Oxfordian) | ![]() | Possessed broad, greatly enlarged shoulder spines | ![]() |
Gilmoreosaurus | 1979 | Bissekty Formation?, Iren Dabasu Formation, Khodzhakul Formation? (Late Cretaceous, Cenomanian) | ![]() ![]() | Several fossils preserve evidence of cancer-induced tumors[47] | ![]() |
Gobihadros | 2019 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | ![]() | Known from multiple specimens representing different growth stages | ![]() |
Gobiraptor | 2019 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Possessed a deep jaw that may be an adaptation to crushing bivalves or seeds[48] | ![]() |
Gobisaurus | 2001 | Ulansuhai Formation (Late Cretaceous, Turonian) | ![]() | Had no tail club but already possessed the stiff tail of derived ankylosaurids[49] | ![]() |
Gobititan | 2003 | Xinminbao Group (Early Cretaceous, Aptian) | ![]() | Retained the fifth digit of the foot, a basal trait | |
Gobivenator | 2014 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | The most completely known Cretaceous troodontid | ![]() |
Gongbusaurus | 1983 | Shaximiao Formation (Late Jurassic, Oxfordian) | ![]() | Only known from a pair of teeth. May be an ankylosaurian[50] | |
Gongpoquansaurus | 2014 | Xinminbao Group (Early Cretaceous, Albian) | ![]() | Remains originally named as a species of Probactrosaurus | ![]() |
Gongxianosaurus | 1998 | Ziliujing Formation (Early Jurassic, Toarcian) | ![]() | The only sauropod with ossified distal tarsals, hinting at its basal position | |
Goyocephale | 1982 | Unnamed formation (Late Cretaceous, Campanian) | ![]() | Had a sloping head with a flat skull roof | ![]() |
Graciliceratops | 2000 | Bayan Shireh Formation (Late Cretaceous, Santonian) | ![]() | Possessed a short frill with large fenestrae | ![]() |
Graciliraptor | 2004 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | A close relative of Microraptor with characteristically slender bones | ![]() |
Guanlong | 2006 | Shishugou Formation (Late Jurassic, Oxfordian) | ![]() | Two specimens have been discovered, one on top of the other | ![]() |
Halszkaraptor | 2017 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | Originally interpreted as a semiaquatic fish hunter similar to a merganser[51] but this hypothesis has been criticized[52] | ![]() |
Hamititan | 2021 | Shengjinkou Formation (Early Cretaceous, Aptian) | ![]() | Known from seven caudal vertebrae and associated elements | ![]() |
Haplocheirus | 2010 | Shishugou Formation (Late Jurassic, Oxfordian) | ![]() | Possessed three long fingers with short claws. Originally described as a basal alvarezsauroid but similarities have been noted with other coelurosaurs[14][53] | ![]() |
Harpymimus | 1984 | Khuren Dukh Formation?/Shinekhudag Formation? (Early Cretaceous, Albian) | ![]() | Mostly toothless but retains a few teeth in the dentary | ![]() |
Haya | 2011 | Javkhlant Formation (Late Cretaceous, Santonian to Campanian) | ![]() | One specimen preserves a large mass of gastroliths | ![]() |
Heishansaurus | 1953 | Minhe Formation (Late Cretaceous, Campanian to Maastrichtian) | ![]() | May be a junior synonym of Pinacosaurus[54] | |
Helioceratops | 2009 | Quantou Formation (Early Cretaceous to Late Cretaceous, Aptian to Cenomanian) | ![]() | Had a distinctively short lower jaw | ![]() |
Hexing | 2012 | Yixian Formation (Early Cretaceous, Valanginian to Barremian) | ![]() | Three or four teeth are known, but they are not well-preserved | ![]() |
Hexinlusaurus | 2005 | Shaximiao Formation (Middle Jurassic, Bajocian) | ![]() | Originally named as a species of Yandusaurus | ![]() |
Heyuannia | 2002 | Barun Goyot Formation, Dalangshan Formation (Late Cretaceous, Maastrichtian) | ![]() ![]() | Fossilized pigments in referred eggshells suggest they were blue-green[55] | ![]() |
Homalocephale | 1974 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Has been suggested to be a juvenile Prenocephale on account of its flat head,[56] but this is no longer thought to be the case[57] | ![]() |
Huabeisaurus | 2000 | Huiquanpu Formation (Late Cretaceous, Cenomanian to Maastrichtian) | ![]() | May be closely related to Tangvayosaurus[58] | ![]() |
Hualianceratops | 2015 | Shishugou Formation (Late Jurassic, Oxfordian) | ![]() | Had a series of bumps around the edge of the beak | ![]() |
Huanansaurus | 2015 | Nanxiong Formation (Late Cretaceous, Campanian to Maastrichtian) | ![]() | Possessed a distinctive short trapezoidal crest | ![]() |
Huanghetitan | 2006 | Haoling Formation, Hekou Group (Early Cretaceous, Aptian to Albian) | ![]() | Had ribs 3 metres (9.8 ft) long, which supported one of the deepest body cavities of any dinosaur[59] | ![]() |
Huangshanlong | 2014 | Hongqin Formation (Middle Jurassic to Late Jurassic, Aalenian to Oxfordian) | ![]() | Known from some bones of the right forelimb | ![]() |
Huaxiagnathus | 2004 | Yixian Formation (Early Cretaceous, Aptian) | ![]() | One of the largest known compsognathids | |
Huayangosaurus | 1982 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | ![]() | Possessed flank osteoderms and a small tail club in addition to plates and spikes | ![]() |
Hudiesaurus | 1997 | Kalaza Formation (Late Jurassic, Tithonian) | ![]() | Had a butterfly-shaped process on its vertebra | ![]() |
Hulsanpes | 1982 | Barun Goyot Formation (Late Cretaceous, Campanian) | ![]() | Closely related to Halszkaraptor but appears to be more cursorial[60] | ![]() |
Ichthyovenator | 2012 | Grès supérieurs Formation (Early Cretaceous, Aptian) | ![]() | One of its sacral vertebrae was greatly reduced, giving the illusion of a break in its sail or of two separate sails | ![]() |
Incisivosaurus | 2002 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | Two specimens of different ontogenetic stages are known, both with differing types of feathers[61] | ![]() |
Irisosaurus | 2020 | Fengjiahe Formation (Early Jurassic, Hettangian) | ![]() | Closely related to Mussaurus[62] | ![]() |
Isanosaurus | 2000 | Nam Phong Formation (Late Triassic, Norian to Rhaetian) | ![]() | May have actually come from the Late Jurassic[63] | ![]() |
Ischioceratops | 2015 | Wangshi Group (Late Cretaceous, Campanian to Maastrichtian) | ![]() | Noted for its peculiarly-shaped ischium | ![]() |
Itemirus | 1976 | Bissekty Formation (Late Cretaceous, Turonian) | ![]() | Originally known from a braincase but abundant new remains were described in 2014[64] | ![]() |
Jaculinykus | 2023 | Barun Goyot Formation (Late Cretaceous, Maastrichtian) | ![]() | Was didactyl, with a large first finger and a reduced second finger | ![]() |
Jaxartosaurus | 1937 | Dabrazhin Formation (Late Cretaceous, Santonian) | ![]() | Not known from many remains but they are enough to tell that it was a basal lambeosaurine[65] | ![]() |
Jeholosaurus | 2000 | Yixian Formation (Early Cretaceous, Aptian) | ![]() | One specimen is preserved in a curled position | ![]() |
Jianchangosaurus | 2013 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | Several characters of its teeth and jaws are convergently similar to those of ornithischians[66] | ![]() |
Jiangjunosaurus | 2007 | Shishugou Formation (Late Jurassic, Oxfordian) | ![]() | Had two rows of circular or diamond-shaped plates | |
Jiangshanosaurus | 2001 | Jinhua Formation (Late Cretaceous, Turonian to Coniacian) | ![]() | A potential member of the Euhelopodidae[67] | |
Jiangxisaurus | 2013 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | ![]() | Overall similar to Heyuannia but with a thinner, frailer mandible | ![]() |
Jiangxititan | 2023 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | ![]() | Described as one of the few known lognkosaurs from mainland Asia | ![]() |
Jianianhualong | 2017 | Yixian Formation (Early Cretaceous, Aptian) | ![]() | Possessed a subtriangular tail frond made of asymmetrical feathers, although it was most likely flightless | ![]() |
Jinbeisaurus | 2019 | Huiquanpu Formation (Late Cretaceous, Cenomanian to Maastrichtian) | ![]() | A medium-sized tyrannosauroid | |
Jinfengopteryx | 2005 | Huajiying Formation (Early Cretaceous, Barremian) | ![]() | May have been capable of some sort of flight[68] | ![]() |
Jingshanosaurus | 1995 | Lufeng Formation (Early Jurassic, Hettangian) | ![]() | One of the latest-surviving non-sauropod sauropodomorphs | ![]() |
Jintasaurus | 2009 | Xinminbao Group (Early Cretaceous, Albian) | ![]() | Known from only the rear half of a skull, including a complete braincase | |
Jinyunpelta | 2018 | Liangtoutang Formation (Early Cretaceous to Late Cretaceous, Albian to Cenomanian) | ![]() | The oldest ankylosaurid known to have a tail club | ![]() |
Jinzhousaurus | 2001 | Yixian Formation (Early Cretaceous, Aptian) | ![]() | Its holotype is nearly complete, preserved whole on a single slab | |
Jiutaisaurus | 2006 | Quantou Formation (Early Cretaceous to Late Cretaceous, Barremian to Cenomanian) | ![]() | Named based on eighteen vertebrae | |
Kaijiangosaurus | 1984 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | ![]() | Potentially synonymous with other medium-sized Shaximiao theropods | ![]() |
Kamuysaurus | 2019 | Hakobuchi Formation (Late Cretaceous, Maastrichtian) | ![]() | Informally referred to as "Mukawaryu" before its formal description | ![]() |
Kansaignathus | 2021 | Ialovachsk Formation (Late Cretaceous, Santonian) | ![]() | The first non-avian dinosaur described from Tajikistan | ![]() |
Kazaklambia | 2013 | Dabrazhin Formation (Late Cretaceous, Santonian) | ![]() | Morphologically distinct from other Eurasian lambeosaurines[69] | ![]() |
Kelmayisaurus | 1973 | Lianmuqin Formation (Early Cretaceous, Valanginian to Albian) | ![]() | One popular book mentions a giant species belonging to this genus,[70] but this referral may be incorrect | ![]() |
Kerberosaurus | 2004 | Tsagayan Formation (Late Cretaceous, Maastrichtian) | ![]() | Potentially a close relative of Edmontosaurus[71] | ![]() |
Khaan | 2001 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | Two morphotypes of chevrons are known, which may be a sexually dimorphic trait[72] | ![]() |
Khulsanurus | 2021 | Barun Goyot Formation (Late Cretaceous, Campanian) | ![]() | Contemporary with Parvicursor but can be distinguished by characters of its caudal vertebrae[73] | |
Kileskus | 2010 | Itat Formation (Middle Jurassic, Bathonian) | ![]() | Uncertain if it possesses the head crest as seen in other proceratosaurids | ![]() |
Kinnareemimus | 2009 | Sao Khua Formation (Early Cretaceous, Valanginian to Barremian) | ![]() | Potentially one of the oldest ornithomimosaurs | ![]() |
Klamelisaurus | 1993 | Shishugou Formation (Middle Jurassic, Callovian) | ![]() | Close relatives included several referred species of Mamenchisaurus[74] | ![]() |
Kol | 2009 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | Had a "hyperarctometatarsus" more strongly pinched than other arctometatarsalian taxa. Described as an alvarezsaurid[75] but has been suggested to be related to Avimimus[76] | |
Koreaceratops | 2011 | Sihwa Formation (Early Cretaceous, Albian) | ![]() | Possessed elongated neural spines on its caudal vertebrae. Its describers suggest that it was used as a swimming organ,[77] but a later study found it to live in a semiarid environment, making this unlikely[78] | ![]() |
Koreanosaurus | 2011 | Seonso Conglomerate (Late Cretaceous, Campanian) | ![]() | Had short but powerful forelimbs suggesting it may have been a quadruped[79] | ![]() |
Koshisaurus | 2015 | Kitadani Formation (Early Cretaceous, Hauterivian) | ![]() | Distinguished from other hadrosauroids by the presence of an antorbital fossa | ![]() |
Kulceratops | 1995 | Khodzhakul Formation (Early Cretaceous, Albian) | ![]() | Only known from fragments of a jaw and teeth | ![]() |
Kulindadromeus | 2014 | Ukureyskaya Formation (Middle Jurassic, Bathonian) | ![]() | An ornithischian that preserves evidence of filaments, suggesting that protofeathers were basal to Dinosauria as a whole | ![]() |
Kundurosaurus | 2012 | Udurchukan Formation (Late Cretaceous, Maastrichtian) | ![]() | May be synonymous with Kerberosaurus[80] | ![]() |
Kuru | 2021 | Barun Goyot Formation (Late Cretaceous, Maastrichtian) | ![]() | Had been informally referred to as "Airakoraptor" prior to its formal description | ![]() |
Laiyangosaurus | 2019 | Wangshi Group (Late Cretaceous, Maastrichtian) | ![]() | Some specimens referred to this edmontosaurin actually belong to kritosaurins and lambeosaurines[81] | ![]() |
Lanzhousaurus | 2005 | Hekou Group (Early Cretaceous, Barremian) | ![]() | Possessed the largest known teeth of any dinosaur | ![]() |
Leshansaurus | 2009 | Shaximiao Formation (Late Jurassic, Oxfordian to Kimmeridgian) | ![]() | Its braincase is nearly identical to that of Piveteausaurus[82] | ![]() |
Levnesovia | 2009 | Bissekty Formation (Late Cretaceous, Turonian) | ![]() | One of the smallest known hadrosauroids[42] | |
Liaoceratops | 2002 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | One specimen was found without a skull roof, possibly displaced by a predator to eat its brain[83] | ![]() |
Liaoningosaurus | 2001 | Yixian Formation (Early Cretaceous, Barremian to Aptian) | ![]() | One specimen has been interpreted as possessing fork-like teeth, sharp claws, and stomach contents including fish, which has been claimed to be evidence of a semi-aquatic, turtle-like lifestyle[84] | ![]() |
Liaoningotitan | 2018 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | The second sauropod named from the Yixian Formation | |
Liaoningvenator | 2017 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | Uniquely preserved with the head curving forwards, differing from the classic theropod "death pose" and the sleeping position of other troodontids | ![]() |
Limusaurus | 2009 | Shishugou Formation (Late Jurassic, Oxfordian) | ![]() | Multiple specimens from different growth stages are known. Juveniles possessed teeth which were lost and replaced with a beak as adults, suggesting a change in diet[85] | ![]() |
Lingwulong | 2018 | Yanan Formation?/Zhiluo Formation? (Middle Jurassic to Late Jurassic, Aalenian to Oxfordian) | ![]() | The first confirmed diplodocoid from Asia. Originally considered Early Jurassic, making it the oldest known neosauropod, but this age has been disputed[86][87] | ![]() |
Lingyuanosaurus | 2019 | Jiufotang Formation?/Yixian Formation? (Early Cretaceous, Valanginian to Aptian) | ![]() | Possessed a mix of basal and derived therizinosaurian traits | ![]() |
Linhenykus | 2011 | Bayan Mandahu Formation (Late Cretaceous, Campanian to Maastrichtian) | ![]() | Completely monodactyl due to lacking the vestigial second and third fingers of other alvarezsaurids | ![]() |
Linheraptor | 2010 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | ![]() | Potentially a synonym of Tsaagan[88] | ![]() |
Linhevenator | 2011 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | ![]() | Had a greatly enlarged sickle claw, comparable in size to those of dromaeosaurids | ![]() |
Liubangosaurus | 2010 | Xinlong Formation (Early Cretaceous, Barremian to Aptian) | ![]() | Described only as a eusauropod[89] but has since been reinterpreted as a somphospondylian[90] | |
Luanchuanraptor | 2007 | Qiupa Formation (Late Cretaceous, Maastrichtian) | ![]() | The first Asian dromaeosaurid found outside the Gobi Desert and northeastern China. May have been closely related to Adasaurus[14] | ![]() |
Lufengosaurus | 1940 | Lufeng Formation (Early Jurassic, Hettangian to Sinemurian) | ![]() | The rib of one specimen preserves the oldest known evidence of collagen proteins[91] | ![]() |
Luoyanggia | 2009 | Haoling Formation (Early Cretaceous, Aptian to Albian) | ![]() | Originally believed to date from the Late Cretaceous | |
Machairasaurus | 2010 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | ![]() | Its hand claws are elongated and blade-like in side view | ![]() |
Mahakala | 2007 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | Possessed basal traits for a dromaeosaurid. May be a close relative of Halszkaraptor[92] | ![]() |
Maleevus | 1987 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | ![]() | Its only purportedly distinguishing trait is also shared with Pinacosaurus[36] | |
Mamenchisaurus | 1954 | Penglaizhen Formation, Shaximiao Formation, Shishugou Formation, Suining Formation (Late Jurassic to Early Cretaceous, Oxfordian to Aptian) | ![]() | Several species have been named, but most may not belong to this genus[74] | ![]() |
Mandschurosaurus | 1930 | Grès supérieurs Formation?, Yuliangze Formation (Late Cretaceous, Maastrichtian) | ![]() ![]() | One of the first non-avian dinosaurs named from Chinese remains | ![]() |
Mei | 2004 | Yixian Formation (Early Cretaceous, Aptian) | ![]() | Two specimens are preserved in bird-like sleeping positions[93] | ![]() |
Microceratus | 2008 | Ulansuhai Formation (Late Cretaceous, Turonian) | ![]() | Originally named Microceratops, although that genus name is preoccupied by a wasp | ![]() |
Microhadrosaurus | 1979 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | ![]() | Reportedly an unusually small hadrosaurid | |
Micropachycephalosaurus | 1978 | Wangshi Group (Late Cretaceous, Campanian to Maastrichtian) | ![]() | Once considered to be a pachycephalosaur, although it is now usually considered to be a ceratopsian[94] | ![]() |
Microraptor | 2000 | Jiufotang Formation (Early Cretaceous, Aptian) | ![]() | Known from over three hundred fossils.[95] Several are well-preserved enough to reveal fine details such as feather covering and an iridescent black coloration[96] | ![]() |
Migmanychion | 2023 | Longjiang Formation (Early Cretaceous, Aptian) | ![]() | Its hand combines features of multiple groups of coelurosaurs | ![]() |
Minimocursor | 2023 | Phu Kradung Formation (Late Jurassic, Tithonian) | ![]() | The first basal neornithischian known from southeastern Asia | ![]() |
Minotaurasaurus | 2009 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | The holotype skull was excavated illegally, which obscured its true provenance until recently | ![]() |
Mongolosaurus | 1933 | On Gong Formation (Early Cretaceous, Aptian to Albian) | ![]() | Known from only scant remains but has been confidently assigned to Somphospondyli in recent years[90] | ![]() |
Mongolostegus | 2018 | Dzunbain Formation (Early Cretaceous, Aptian to Albian) | ![]() | Informally assigned to the genus Wuerhosaurus before its formal description | ![]() |
Monkonosaurus | 1986 | Loe-ein Formation?/Lura Formation? (Late Jurassic, Oxfordian to Kimmeridgian?/Early Cretaceous, Albian?) | ![]() | Poorly known | |
Monolophosaurus | 1993 | Shishugou Formation (Middle Jurassic, Bathonian to Callovian) | ![]() | Possessed a short, rectangular crest running along the midline of the skull | ![]() |
Mononykus | 1993 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Proposed to have an anteater-like lifestyle, using its unique forearms to break into termite mounds[97] | ![]() |
Mosaiceratops | 2015 | Xiaguan Formation (Late Cretaceous, Turonian to Campanian) | ![]() | Combined features of different groups of basal ceratopsians | ![]() |
Nankangia | 2013 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | ![]() | May have specialized in soft foods such as leaves and seeds[98] | ![]() |
Nanningosaurus | 2007 | Unnamed formation (Late Cretaceous, Maastrichtian) | ![]() | Potentially a basal lambeosaurine | |
Nanshiungosaurus | 1979 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | ![]() | Originally misidentified as a sauropod on account of its unusual pelvis | ![]() |
Nanyangosaurus | 2000 | Xiaguan Formation (Late Cretaceous, Turonian to Campanian) | ![]() | Completely lost the first digit of its hands | ![]() |
Napaisaurus | 2022 | Xinlong Formation (Early Cretaceous, Aptian to Albian) | ![]() | May be closely related to contemporary Thai iguanodonts | |
Natovenator | 2022 | Barun Goyot Formation (Late Cretaceous, Maastrichtian) | ![]() | Possessed a streamlined body and a long, toothed snout, convergently similar to several groups of aquatic vertebrates | ![]() |
Nebulasaurus | 2015 | Zhanghe Formation (Middle Jurassic, Aalenian to Bajocian) | ![]() | Only known from a single braincase, but it is enough to tell that it was related to Spinophorosaurus | ![]() |
Neimongosaurus | 2001 | Iren Dabasu Formation (Late Cretaceous, Cenomanian) | ![]() | Could extend its arms considerably forward due to the structure of its shoulder joint[99] | ![]() |
Nemegtomaia | 2005 | Barun Goyot Formation, Nemegt Formation (Late Cretaceous, Campanian to Maastrichtian) | ![]() | One specimen preserves traces of damage by skin beetles[100] | ![]() |
Nemegtonykus | 2019 | Nemegt Formation (Late Cretaceous, Campanian to Maastrichtian) | ![]() | The second alvarezsaurid named from the Nemegt Formation | ![]() |
Nemegtosaurus | 1971 | Nemegt Formation, Subashi Formation? (Late Cretaceous, Maastrichtian) | ![]() ![]() | Had a long, low skull similar in proportions to those of diplodocoids | ![]() |
Ningyuansaurus | 2012 | Yixian Formation (Early Cretaceous, Aptian) | ![]() | Preserves small oval-shaped structures in its stomach region which may be seeds | |
Nipponosaurus | 1936 | Yezo Group (Late Cretaceous, Santonian to Campanian) | ![]() | Discovered on the island of Sakhalin, which was owned by Japan in 1936 but later annexed by Russia | ![]() |
Oksoko | 2020 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Its third finger was so greatly reduced that it was functionally didactyl | ![]() |
Olorotitan | 2003 | Udurchukan Formation (Late Cretaceous, Maastrichtian) | ![]() | Had a broad, hatchet-shaped crest | ![]() |
Omeisaurus | 1939 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | ![]() | Members of this genus are characterized by extremely elongated necks | ![]() |
Ondogurvel | 2022 | Barun Goyot Formation (Late Cretaceous, (Campanian) | ![]() | Known from well-preserved remains of the hands and feet | ![]() |
Opisthocoelicaudia | 1977 | Nemegt Formation (Late Cretaceous, Campanian to Maastrichtian) | ![]() | Walked on its metacarpals due to its complete lack of phalanges | ![]() |
Oviraptor | 1924 | Djadochta Formation (Late Cretaceous, Campanian to Maastrichtian) | ![]() | Originally mistakenly thought to be an egg-eater | ![]() |
Pachysuchus | 1951 | Lufeng Formation (Early Jurassic, Sinemurian to Pliensbachian) | ![]() | Considered a phytosaur from its original naming until a redescription in 2012[101] | |
Panguraptor | 2014 | Lufeng Formation (Early Jurassic, Hettangian to Sinemurian) | ![]() | The first definitive coelophysoid known from Asia | |
Papiliovenator | 2021 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | ![]() | Had a short, subtriangular skull similar to those of Early Cretaceous troodontids | ![]() |
Paralitherizinosaurus | 2022 | Yezo Group (Late Cretaceous, Campanian | ![]() | Had stiffened claws that may have been used to pull vegetation to the mouth[102] | ![]() |
Parvicursor | 1996 | Barun Goyot Formation (Late Cretaceous, Campanian) | ![]() | Originally believed to represent a diminutive adult dinosaur, although it was recently reinterpreted as a juvenile[103] | ![]() |
Pedopenna | 2005 | Haifanggou Formation (Middle Jurassic, Callovian) | ![]() | Known from a single leg with the impressions of long, symmetrical feathers | ![]() |
Peishansaurus | 1953 | Minhe Formation (Late Cretaceous, Santonian to Campanian) | ![]() | Has been compared to thyreophorans and marginocephalians, but it is impossible to determine which assignment is correct | |
Penelopognathus | 2005 | Bayin-Gobi Formation (Early Cretaceous, Albian) | ![]() | Named from a single dentary | |
Phaedrolosaurus | 1973 | Lianmuqin Formation (Early Cretaceous, Valanginian to Albian) | ![]() | May have been a dromaeosaurid[104] | |
Philovenator | 2012 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | ![]() | Closely related to the contemporary Linhevenator[93] but likely represents a separate taxon[105] | ![]() |
Phuwiangosaurus | 1994 | Sao Khua Formation (Early Cretaceous, Valanginian to Hauterivian) | ![]() | A large member of the Euhelopodidae[90] | ![]() |
Phuwiangvenator | 2019 | Sao Khua Formation (Early Cretaceous, Barremian) | ![]() | Combines features of both allosauroids and coelurosaurs[106] | ![]() |
Pinacosaurus | 1933 | Bayan Mandahu Formation, Djadochta Formation (Late Cretaceous, Santonian to Campanian) | ![]() ![]() | May have been capable of bird-like vocalizations[107] | ![]() |
Plesiohadros | 2014 | Alagteeg Formation (Late Cretaceous, Campanian) | ![]() | The first hadrosauroid known from the Alagteeg Formation | |
Prenocephale | 1974 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Had a distinctively conical dome | ![]() |
Probactrosaurus | 1966 | Dashuigou Formation (Early Cretaceous, Albian) | ![]() | The closest relative to the Hadrosauromorpha based on the definition of the group[108] | ![]() |
Prodeinodon | 1924 | Öösh Formation, Xinlong Formation (Early Cretaceous, Barremian to Aptian) | ![]() ![]() | Potentially a carnosaur[109] | |
Protarchaeopteryx | 1997 | Yixian Formation (Early Cretaceous, Aptian) | ![]() | Usually thought to be a basal oviraptorosaur but one study suggests a basal position within Pennaraptora[14] | ![]() |
Protoceratops | 1923 | Bayan Mandahu Formation, Djadochta Formation (Late Cretaceous, Campanian) | ![]() ![]() | Its remains are so abundant that it has been nicknamed the "sheep of the Cretaceous" | ![]() |
Protognathosaurus | 1991 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | ![]() | Originally named Protognathus, but that is preoccupied by an extinct beetle[110] | |
Psittacosaurus | 1923 | Andakhuduk Formation, Bayin-Gobi Formation, Ejinhoro Formation, Ilek Formation, Jiufotang Formation, Khok Kruat Formation, Öösh Formation, Qingshan Formation, Tugulu Group, Xinminbao Group, Yixian Formation (Early Cretaceous, Barremian to Albian) | ![]() ![]() ![]() ![]() | Known from hundreds of specimens, many of them well-preserved. Lived in a broad range | ![]() |
Pukyongosaurus | 2001 | Hasandong Formation (Early Cretaceous, Aptian to Albian) | ![]() | One of its caudal vertebrae has bite marks caused by theropod teeth | ![]() |
Qianlong | 2023 | Ziliujing Formation (Early Jurassic, Sinemurian) | ![]() | Associated with fossils of leathery eggs, the oldest of their kind in the world | ![]() |
Qianzhousaurus | 2014 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | ![]() | Has been nicknamed "Pinocchio rex" on account of its elongated snout | ![]() |
Qiaowanlong | 2009 | Xinminbao Group (Early Cretaceous, Albian) | ![]() | Originally described as a brachiosaurid[111] but has since been reinterpreted as a euhelopodid[112] | |
Qijianglong | 2015 | Suining Formation (Early Cretaceous, Aptian) | ![]() | Once believed to date from the Late Jurassic | |
Qingxiusaurus | 2008 | Unnamed formation (Late Cretaceous, Maastrichtian) | ![]() | Known from very limited remains | |
Qinlingosaurus | 1996 | Hongtuling Formation?/Shanyang Formation? (Late Cretaceous, Maastrichtian) | ![]() | Potentially a titanosaur given its age, but this cannot be confirmed | ![]() |
Qiupalong | 2011 | Qiupa Formation (Late Cretaceous, Campanian to Maastrichtian) | ![]() | A referred specimen was found in Canada[113] | ![]() |
Qiupanykus | 2018 | Qiupa Formation (Late Cretaceous, Maastrichtian) | ![]() | May have used its robust thumb claws to crack open oviraptorid eggshells[114] | |
Quaesitosaurus | 1983 | Barun Goyot Formation (Late Cretaceous, Maastrichtian) | ![]() | Potentially a close relative of Nemegtosaurus | ![]() |
Ratchasimasaurus | 2011 | Khok Kruat Formation (Early Cretaceous, Aptian) | ![]() | Only known from a single toothless dentary | ![]() |
Rhomaleopakhus | 2021 | Kalaza Formation (Late Jurassic, Tithonian) | ![]() | Possessed a robust forelimb that may be a locomotory adaptation | ![]() |
Rinchenia | 1997 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Had a tall, domed crest | ![]() |
Ruixinia | 2022 | Yixian Formation (Early Cretaceous, Barremian) | ![]() | Its last few caudal vertebrae were fused into a rod-like structure | |
Ruyangosaurus | 2009 | Haoling Formation (Early Cretaceous, Aptian to Albian) | ![]() | Only known from scant remains but was one of the largest dinosaurs known from Asia | ![]() |
Sahaliyania | 2008 | Yuliangze Formation (Late Cretaceous, Maastrichtian) | ![]() | Possibly a synonym of Amurosaurus[115] | ![]() |
Saichania | 1977 | Barun Goyot Formation, Nemegt Formation (Late Cretaceous, Campanian to Maastrichtian) | ![]() | Possessed complicated nasal passages that may have cooled the air it breathed | ![]() |
Sanpasaurus | 1944 | Ziliujing Formation (Early Jurassic, Toarcian) | ![]() | Historically conflated with the remains of an ornithischian | ![]() |
Sanxiasaurus | 2019 | Xintiangou Formation (Middle Jurassic, Bajocian) | ![]() | The oldest neornithischian known from Asia | ![]() |
Saurolophus | 1912 | Nemegt Formation (Late Cretaceous, Maastrichtian) | ![]() | Type species was found in Canada. The Asian species is distinguished by its larger size and backwards-pointing diagonal crest | ![]() |
Sauroplites | 1953 | Zhidan Group (Early Cretaceous, Barremian to Aptian) | ![]() | Preserved lying on its back with parts of its armor in an articulated position | |
Saurornithoides | 1924 | Djadochta Formation (Late Cretaceous, Campanian) | ![]() | Its hindlimbs were well-developed even as juveniles, suggesting it needed little to no parental care | ![]() |
Scansoriopteryx | 2002 | Haifanggou Formation (Middle Jurassic to Late Jurassic, Callovian to Kimmeridgian) | ![]() | Was well-adapted for climbing due to the structure of its hands and feet | ![]() |
Segnosaurus | 1979 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Turonian) | ![]() | One of the first known therizinosaurs. Its relationships were originally obscure | ![]() |
Serikornis | 2017 | Tiaojishan Formation (Middle Jurassic to Late Jurassic, Callovian to Oxfordian) | ![]() | Possessed simple, wispy feathers similar to those of a Silkie chicken | ![]() |
Shamosaurus | 1983 | Dzunbain Formation (Early Cretaceous, Aptian to Albian) | ![]() | The osteoderms on its head were not separated into obvious tiles as with later ankylosaurs | |
Shanag | 2007 | Öösh Formation (Early Cretaceous, Berriasian to Barremian) | ![]() | Shows a mixture of traits of various paravian groups | ![]() |
Shantungosaurus | 1973 | Wangshi Group (Late Cretaceous, Campanian) | ![]() | The largest known hadrosaurid | ![]() |
Shanxia | 1998 | Huiquanpu Formation (Late Cretaceous, Cenomanian to Campanian) | ![]() | May be synonymous with Tianzhenosaurus[116] and/or Saichania[36] | |
Shanyangosaurus | 1996 | Shanyang Formation (Late Cretaceous, Maastrichtian) | ![]() | Indeterminate but its hollow bones are a synapomorphy for Coelurosauria. One study suggests an oviraptorosaurian position[14] | |
Shaochilong | 2009 | Ulansuhai Formation (Late Cretaceous, Cenomanian to Turonian) | ![]() | Had a relatively short maxilla, suggesting a unique ecological role | ![]() |
Shenzhousaurus | 2003 | Yixian Formation (Early Cretaceous, Aptian) | ![]() | Preserves pebbles in its thoracic cavity which may be gastroliths | ![]() |
Shidaisaurus | 2009 | Chuanjie Formation (Middle Jurassic, Aalenian) | ![]() | Potentially one of the oldest known allosauroids | ![]() |
Shishugounykus | 2019 | Shishugou Formation (Late Jurassic, Oxfordian) | ![]() | Its manus combines features of both alvarezsaurians and more basal coelurosaurs | ![]() |
Shixinggia | 2005 | Pingling Formation (Late Cretaceous, Maastrichtian) | ![]() | Known from a fair amount of postcranial material | |
Shri | 2021 | Barun Goyot Formation (Late Cretaceous, Maastrichtian) | ![]() | Before its formal description, it was nicknamed "Ichabodcraniosaurus" because its holotype lacked a skull | ![]() |
Shuangmiaosaurus | 2003 | Sunjiawan Formation (Early Cretaceous, Albian) | ![]() |