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. This list does not include dinosaurs that live or lived after the Mesozoic era such as birds.
| Name | Year | Formation | Location | Notes | Images |
|---|---|---|---|---|---|
| Abdarainurus | 2020 | Alagteeg Formation (Late Cretaceous, Santonian to Campanian) | Mongolia | Inconsistent in phylogenetic placement; could represent an unknown lineage of macronarians[1] | |
| Abrosaurus | 1989 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | China | Had unusually large nasal openings in its skull | |
| Achillobator | 1999 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Turonian) | Mongolia | Large, deep-chested and powerfully muscled | |
| Adasaurus | 1983 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Its sickle claw was markedly reduced compared to other dromaeosaurids | |
| Aepyornithomimus | 2017 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | The first ornithomimosaur named from the Djadochta Formation | |
| Agilisaurus | 1983 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | China | 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) | Japan | A possible early ceratopsian known from fragments of a skull | |
| Albinykus | 2011 | Javkhlant Formation (Late Cretaceous, Santonian) | Mongolia | Preserved in a sitting position not unlike that of modern birds | |
| Alectrosaurus | 1933 | Iren Dabasu Formation (Late Cretaceous, Cenomanian) | China | Had long legs which may be an adaptation to pursuit predation | |
| Alioramus | 1976 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Possessed an elongated snout with two rows of five bumps | |
| Almas | 2017 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | Preserved alongside eggshells which may have come from a troodontid[2] | |
| Altirhinus | 1998 | Khuren Dukh Formation (Early Cretaceous, Aptian to Albian) | Mongolia | Had a distinctive, elevated nasal bone with a large nasal cavity to match | |
| Alxasaurus | 1993 | Bayin-Gobi Formation (Early Cretaceous, Albian) | China | Most of the skeleton is known, which allowed researchers to connect therizinosaurs to other theropods | |
| Ambopteryx | 2019 | Unnamed formation (Late Jurassic, Oxfordian) | China | Preserves a "styliform element" that supported a membranous wing as in its relative, Yi | |
| Amtocephale | 2011 | Bayan Shireh Formation (Late Cretaceous, Turonian to Santonian) | Mongolia | One of the oldest known pachycephalosaurs | |
| Amurosaurus | 1991 | Udurchukan Formation (Late Cretaceous, Maastrichtian) | Russia | Discovered in the city of Blagoveshchensk on the border with China | |
| Analong | 2020 | Chuanjie Formation (Middle Jurassic, Bajocian) | China | Known from a partial skeleton originally assigned to Chuanjiesaurus but separated due to several morphological differences | |
| Anchiornis | 2009 | Tiaojishan Formation (Late Jurassic, Oxfordian) | China | Analysis of fossilized melanosomes suggest a mostly gray or black body, white and black patterns on its wings, and a red head crest[3] | |
| Anhuilong | 2020 | Hongqin Formation (Middle Jurassic, Aalenian to Callovian) | China | Closely related to Huangshanlong and Omeisaurus | |
| Anomalipes | 2018 | Wangshi Group (Late Cretaceous, Maastrichtian) | China | May have been closely related to Gigantoraptor despite its significantly smaller size[4] | |
| Anserimimus | 1988 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Had uniquely powerful forelimbs with peculiarly flattened claws | |
| Aorun | 2013 | Shishugou Formation, (Late Jurassic, Oxfordian) | China | Potentially a basal member of the alvarezsaurian lineage[5] | |
| Aralosaurus | 1968 | Bostobe Formation, (Late Cretaceous, Santonian to Campanian) | Kazakhstan | A basal lambeosaurine hadrosaurid with a large, solid crest | |
| Archaeoceratops | 1997 | Xinminbao Group (Early Cretaceous, Xinminbao Group) | China | Had no horns and only the beginnings of a frill | |
| Archaeornithoides | 1992 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | Known from only a partial skull with scratches that may have been created by a small mammal[6] | |
| Archaeornithomimus | 1972 | Iren Dabasu Formation (Late Cretaceous, Cenomanian) | China | Unlike other ornithomimosaurs, its feet were not arctometatarsalian | |
| Arkharavia | 2010 | Udurchukan Formation (Late Cretaceous, Maastrichtian) | Russia | Described as a sauropod[7] but a referred vertebra belongs to a hadrosaurid[8] | |
| Arstanosaurus | 1982 | Bostobe Formation (Late Cretaceous, Santonian to Campanian) | Kazakhstan | Poorly known | |
| Asiaceratops | 1989 | Khodzhakul Formation (Late Cretaceous, Cenomanian) | Uzbekistan | Leptoceratopsid affinities have been suggested[9] | |
| Asiatosaurus | 1924 | Öösh Formation, Xinlong Formation (Early Cretaceous, Aptian) | China Mongolia |
Two species have been named but both are only known from extremely scant remains | |
| Auroraceratops | 2005 | Xinminbao Group (Early Cretaceous, Aptian) | China | A basal, bipedal ceratopsian closely related to Archaeoceratops | |
| Aurornis | 2013 | Tiaojishan Formation (Late Jurassic, Oxfordian) | China | 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) | Mongolia | Bonebed remains indicate a gregarious lifestyle; it may have formed age-segregated herds for lekking or flocking purposes[10] | |
| Bactrosaurus | 1933 | Iren Dabasu Formation, Majiacun Formation (Late Cretaceous, Cenomanian | China | Remains of six individuals are known, making up much of the skeleton | |
| Bagaceratops | 1975 | Barun Goyot Formation, Djadochta Formation (Late Cretaceous, Maastrichtian) | Mongolia | May have been a direct descendant of Protoceratops to which it physically resembles[11] | |
| Bagaraatan | 1996 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Combines traits of several theropod groups | |
| Bainoceratops | 2003 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | Its supposedly diagnostic features may fall within Protoceratops variation[12] | |
| Banji | 2010 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | China | Vertical striations adorned the sides of its crest | |
| Bannykus | 2018 | Bayin-Gobi Formation (Early Cretaceous, Aptian) | China | 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) | China | Large but known from only a few bones | |
| Barsboldia | 1981 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Possessed elongated neural spines particularly above the hips | |
| Batyrosaurus | 2012 | Bostobe Formation (Late Cretaceous, Santonian to Campanian) | Kazakhstan | Remains originally identified as Arstanosaurus | |
| Bayannurosaurus | 2018 | Bayin-Gobi Formation (Early Cretaceous, Aptian) | China | A large basal iguanodontian noted for its "perfect" preservation | |
| Beg | 2020 | Ulaanoosh Formation (Early Cretaceous to Late Cretaceous, Albian to Cenomanian) | Mongolia | Had a rounded skull with a rugose texture | |
| Beibeilong | 2017 | Gaogou Formation (Late Cretaceous, Cenomanian to Turonian) | China | Similar to but more basal than Gigantoraptor.[13] Known from only a single embryo still in its egg | |
| Beipiaosaurus | 1999 | Yixian Formation (Early Cretaceous, Aptian) | China | Preserves evidence of downy feathers as well as a secondary coat of simpler "elongated broad filamentous feathers" or EBFFs[14] | |
| Beishanlong | 2010 | Xiagou Formation (Early Cretaceous, Aptian to Albian) | China | Lacked the elongated claws of more derived ornithomimosaurs | |
| Bellusaurus | 1990 | Shishugou Formation (Middle Jurassic, Bajocian) | China | Known from a bone bed with the remains of seventeen juvenile specimens | |
| Bienosaurus | 2001 | Lufeng Formation (Early Jurassic, Sinemurian) | China | Potentially synonymous with Tatisaurus[15] | |
| Bissektipelta | 2004 | Bissekty Formation (Late Cretaceous, Turonian to Coniacian) | Uzbekistan | Analysis of its braincase suggests poor hearing and eyesight but good olfaction and taste; it may have been a filter feeder[16] | |
| Bolong | 2010 | Yixian Formation (Early Cretaceous, Aptian) | China | Originally known from only a skull; an almost complete skeleton was described in 2013[17] | |
| Borealosaurus | 2004 | Sunjiawan Formation (Late Cretaceous, Cenomanian to Turonian) | China | Its caudal vertebrae were distinctively opisthocoelous | |
| Borogovia | 1987 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Had a uniquely straight and flattened sickle claw, which may have had a weight-bearing function | |
| Breviceratops | 1990 | Barun Goyot Formation (Late Cretaceous, Campanian) | Mongolia | Only known from juvenile remains but can be distinguished from other protoceratopsids | |
| Brohisaurus | 2003 | Sembar Formation (Late Jurassic, Kimmeridgian) | Pakistan | Possibly one of the oldest known titanosauriforms | |
| Byronosaurus | 2000 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | Two skulls from juveniles of this troodontid have been recovered in an oviraptorid nest | |
| Caenagnathasia | 1994 | Bissekty Formation (Late Cretaceous, Turonian to Coniacian) | Uzbekistan | One of the oldest and smallest known caenagnathoids | |
| Caihong | 2018 | Tiaojishan Formation (Late Jurassic, Oxfordian) | China | Possessed platelet-shaped melanosomes that produced iridesence as in modern trumpeters | |
| Caudipteryx | 1998 | Yixian Formation (Early Cretaceous, Aptian) | China | Did not have secondary feathers attached to the lower arm | |
| Ceratonykus | 2009 | Barun Goyot Formation (Late Cretaceous, Campanian) | Mongolia | Shares several osteological features with ornithischians | |
| Changchunsaurus | 2005 | Quantou Formation (Early Cretaceous to Late Cretaceous, Albian to Cenomanian) | China | Had wavy enamel on its leaf-shaped teeth that made them more resistant to wear; this feature is also present in hadrosaurs[18] | |
| Changmiania | 2020 | Yixian Formation (Early Cretaceous, Barremian) | China | Preserved in a sleeping position curled up in a potential burrow | |
| Changyuraptor | 2014 | Yixian Formation (Early Cretaceous, Aptian) | China | The largest microraptorian dromaeosaurid known. Had tail feathers almost a foot long[19] | |
| Chaoyangsaurus | 1999 | Tuchengzi Formation (Late Jurassic, Tithonian) | China | Known by a number of alternate spellings (e.g. Chaoyangosaurus, Chaoyoungosaurus) before its formal description | |
| Charonosaurus | 2000 | Yuliangze Formation (Late Cretaceous, Maastrichtian) | China | May have had a long, backwards-arcing crest similar to that of Parasaurolophus | |
| Chialingosaurus | 1959 | Shaximiao Formation (Late Jurassic, Oxfordian to Kimmeridgian) | China | Had both large plates and smaller spines, similar to Kentrosaurus | |
| Chiayusaurus | 1953 | Hasandong Formation, Xinminbao Group (Early Cretaceous, Barremian to Aptian) | China South Korea |
Two species have been named, both from teeth. Those of C. lacustris are apparently indistinguishable to those of Euhelopus[20] or Mamenchisaurus[21] | |
| Chilantaisaurus | 1964 | Ulansuhai Formation (Late Cretaceous, Turonian) | China | A large theropod with a particularly hooked claw on its first finger | |
| Chingkankousaurus | 1958 | Wangshi Group (Late Cretaceous, Santonian to Campanian) | China | Possibly a tyrannosauroid;[22] known from only a scapula | |
| Chinshakiangosaurus | 1992 | Fengjiahe Formation (Early Jurassic, Hettangian) | China | Had a U-shaped snout that may have supported fleshy cheeks, an adaptation to bulk feeding | |
| Choyrodon | 2018 | Khuren Dukh Formation (Early Cretaceous, Albian) | Mongolia | It had an enlarged nose similar to its contemporary, Altirhinus, but it is most likely a separate taxon[23] | |
| Chuandongocoelurus | 1984 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | China | A tetanuran of uncertain relationships | |
| Chuanjiesaurus | 2000 | Chuanjie Formation (Middle Jurassic, Bathonian) | China | One of the more derived mamenchisaurids[24] | |
| Chuanqilong | 2014 | Jiufotang Formation (Early Cretaceous, Aptian) | China | May have been the adult form of the coeval Liaoningosaurus[25] | |
| Chungkingosaurus | 1983 | Shaximiao Formation (Late Jurassic, Oxfordian) | China | 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) | China | Potentially a synonym of Jingshanosaurus[26] | |
| Citipati | 2001 | Djadochta Formation (Late Cretaceous, Campanian to Maastrichtian) | Mongolia | 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[27] | |
| Conchoraptor | 1986 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Named for a hypothesized diet of shellfish, but this cannot be confirmed | |
| Corythoraptor | 2017 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | China | Its crest was vertical and rectangular, not unlike that of a cassowary | |
| Crichtonpelta | 2015 | Sunjiawan Formation (Late Cretaceous, Cenomanian) | China | Originally named as a second species of Crichtonsaurus | |
| Crichtonsaurus | 2002 | Sunjiawan Formation (Late Cretaceous, Cenomanian to Turonian) | China | Sometimes reconstructed with semicircular osteoderms vaguely similar to the plates of stegosaurs | |
| Daanosaurus | 2005 | Shaximiao Formation (Late Jurassic, Oxfordian to Tithonian) | China | Only known from the remains of a juvenile | |
| Daliansaurus | 2017 | Yixian Formation (Early Cretaceous, Barremian) | China | 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) | China | Reportedly a Camarasaurus-like sauropod | |
| Datanglong | 2014 | Xinlong Formation (Early Cretaceous, Barremian to Albian) | China | Had a uniquely pneumatized ilium similar to megaraptorans | |
| Datonglong | 2016 | Huiquanpu Formation (Late Cretaceous, Cenomanian to Campanian) | China | Precise dating uncertain | |
| Datousaurus | 1984 | Shaximiao Formation (Middle Jurassic, Callovian) | China | One of the rarer sauropods of the Shaximiao, known from only two skeletons and a large, deep skull | |
| Daxiatitan | 2008 | Hekou Group (Early Cretaceous, Barremian) | China | Large and very long-necked | |
| Deinocheirus | 1970 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Had a suite of unique features, most notably a hump supported by elongated neural spines | |
| Dilong | 2004 | Yixian Formation (Early Cretaceous, Barremian) | China | Preserves evidence of a coating of simple feathers | |
| Dongbeititan | 2007 | Yixian Formation (Early Cretaceous, Barremian) | China | A tooth referred to Sinocalliopteryx has been found encrusted in one of its ribs[28] | |
| Dongyangopelta | 2013 | Chaochuan Formation (Early Cretaceous to Late Cretaceous, Albian to Cenomanian) | China | Coexisted with Zhejiangosaurus but could be distinguished based on subtle osteological features[29] | |
| Dongyangosaurus | 2008 | Fangyan Formation (Late Cretaceous, Cenomanian to Santonian) | China | A titanosauriform of uncertain phylogenetic placement | |
| Dzharatitanis | 2021 | Bissekty Formation (Late Cretaceous, Turonian) | Uzbekistan | Originally described as a rebbachisaurid[30] but later hypothesized to be titanosaur with possible lognkosaurian affinities[31] | |
| Elmisaurus | 1981 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | One of the most complete caenagnathids known | |
| Embasaurus | 1931 | Neocomian Sands (Early Cretaceous, Berriasian) | Kazakhstan | Known from only two vertebrae | |
| Enigmosaurus | 1983 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | Mongolia | Had a large, backwards-pointing pelvis | |
| Eomamenchisaurus | 2008 | Zhanghe Formation (Middle Jurassic, Aalenian to Callovian) | China | One of the oldest mamenchisaurids, having primitive traits | |
| Eosinopteryx | 2013 | Tiaojishan Formation (Late Jurassic, Oxfordian) | China | Lacked advanced tail feathers and long "hind wings", unlike other paravians | |
| Epidexipteryx | 2008 | Daohugou Beds? (Middle Jurassic, Callovian) | China | Supported four long feathers from an abbreviated tail | |
| Equijubus | 2003 | Xinminbao Group (Early Cretaceous, Aptian) | China | A grazer that preserves the oldest known evidence of grass-eating[32] | |
| Erketu | 2006 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | Mongolia | May have had the longest neck of any dinosaur relative to its body | |
| Erliansaurus | 2002 | Iren Dabasu Formation (Late Cretaceous, Cenomanian) | China | Had long, curved claws on its fingers | |
| Erlikosaurus | 1980 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | Mongolia | Preserves the most complete skull known from any therizinosaur | |
| Eshanosaurus | 2001 | Lufeng Formation (Early Jurassic, Hettangian) | China | Has been suggested to be the oldest known therizinosaur | |
| Euhelopus | 1956 | Meng-Yin Formation (Early Cretaceous, Berriasian to Valanginian) | China | Once widely believed to be closely related to mamenchisaurids | |
| Euronychodon | 1991 | Bissekty Formation (Late Cretaceous, Turonian) | Uzbekistan | Type species was found in Portugal. The Asian species may represent a form taxon of improperly developed teeth[33] | |
| Ferganasaurus | 2003 | Balabansai Formation (Middle Jurassic, Callovian) | Kyrgyzstan | Claimed to have two hand claws, but this is disputed[34] | |
| Ferganocephale | 2005 | Balabansai Formation (Middle Jurassic, Callovian) | Kyrgyzstan | Unusually, its teeth were not serrated | |
| Fukuipteryx | 2019 | Kitadani Formation (Early Cretaceous, Aptian) | Japan | A basal avialan known from partial, but three dimensional remains | |
| Fukuiraptor | 2000 | Kitadani Formation, Sebayashi Formation (Early Cretaceous, Barremian to Aptian) | Japan | Similarly to Megaraptor, it was originally reconstructed as a dromaeosaur with its hand claw on its foot | |
| Fukuisaurus | 2003 | Kitadani Formation (Early Cretaceous, Barremian) | Japan | The elements of its skull are so strongly fused that it was unable to chew[35] | |
| Fukuititan | 2010 | Kitadani Formation (Early Cretaceous, Barremian to Aptian) | Japan | The first sauropod named from Japan | |
| Fukuivenator | 2016 | Kitadani Formation (Early Cretaceous, Barremian to Aptian) | Japan | Possesses traits of various groups of coelurosaurs. May have been a herbivore or omnivore due to its heterodont dentition | |
| Fulengia | 1977 | Lufeng Formation (Early Jurassic, Hettangian to Pliensbachian) | China | May have been a juvenile Lufengosaurus | |
| Fushanosaurus | 2019 | Shishugou Formation (Late Jurassic, Oxfordian to Kimmeridgian) | China | Known from a single femur of immense size | |
| Fusuisaurus | 2006 | Xinlong Formation (Early Cretaceous, Aptian to Albian) | China | A referred humerus may support an extremely large size for this taxon[36] | |
| Gallimimus | 1972 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Had a relatively long beak with a rounded tip | |
| Gannansaurus | 2013 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | China | Shares a certain feature of its vertebrae exclusively with Euhelopus | |
| Ganzhousaurus | 2013 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | China | Coexisted with at least seven other oviraptorosaurs, which may have niche-partitioned. It was likely primarily herbivorous[37] | |
| Garudimimus | 1981 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Turonian) | Mongolia | Was not as well-adapted to running as later ornithomimosaurs | |
| Gasosaurus | 1985 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | China | Discovered as a by-product of construction work | |
| Gigantoraptor | 2007 | Iren Dabasu Formation (Late Cretaceous, Cenomanian) | China | The largest known oviraptorosaur, comparable in size to Albertosaurus | |
| Gigantspinosaurus | 1992 | Shaximiao Formation (Late Jurassic, Oxfordian) | China | Possessed broad, greatly enlarged shoulder spines | |
| Gilmoreosaurus | 1979 | Iren Dabasu Formation (Late Cretaceous, Cenomanian) | China Uzbekistan? |
Several fossils preserve evidence of cancer-induced tumors[38] | |
| Gobihadros | 2019 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | Mongolia | Known from multiple specimens representing different growth stages | |
| Gobiraptor | 2019 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Possessed a deep jaw that may be an adaptation to crushing bivalves or seeds[39] | |
| Gobisaurus | 2001 | Ulansuhai Formation (Late Cretaceous, Turonian) | China | Had no tail club but already possessed the stiff tail of derived ankylosaurids[40] | |
| Gobititan | 2003 | Xinminbao Group (Early Cretaceous, Barremian) | China | Retained the fifth digit of the foot, a basal trait | |
| Gobivenator | 2014 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | The most completely known Cretaceous troodontid | |
| Gongbusaurus | 1983 | Shaximiao Formation (Late Jurassic, Oxfordian) | China | Only known from a pair of teeth. May be an ankylosaurian[41] | |
| Gongpoquansaurus | 2014 | Zhongguo Formation (Early Cretaceous, Albian) | China | Remains originally named as a species of Probactrosaurus | |
| Gongxianosaurus | 1998 | Ziliujing Formation (Early Jurassic, Toarcian) | China | Basally retained ossified distal tarsals | |
| Goyocephale | 1982 | Unnamed formation (Late Cretaceous, Campanian) | Mongolia | Had a sloping head with a flat skull roof | |
| Graciliceratops | 2000 | Bayan Shireh Formation (Late Cretaceous, Santonian) | Mongolia | Possessed a short frill with large fenestrae | |
| Graciliraptor | 2004 | Yixian Formation (Early Cretaceous, Barremian) | China | A close relative of Microraptor with characteristically slender bones | |
| Guanlong | 2006 | Shishugou Formation (Late Jurassic, Oxfordian) | China | Two specimens have been discovered, one on top of the other | |
| Halszkaraptor | 2017 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | The proportions of its body suggest it was a semiaquatic fish hunter like a merganser[42] | |
| Hamititan | 2021 | Shengjinkou Formation (Early Cretaceous, Aptian) | China | Known from seven caudal vertebrae and associated elements | |
| Haplocheirus | 2010 | Shishugou Formation (Late Jurassic, Oxfordian) | China | Possessed a basal hand morphology for an alvarezsaur, having three long fingers with short claws | |
| Harpymimus | 1984 | Shinekhudag Formation (Early Cretaceous, Albian) | Mongolia | Mostly toothless but retains a few teeth in the lower dentary | |
| Haya | 2011 | Javkhlant Formation (Late Cretaceous, Santonian to Campanian) | Mongolia | One specimen preserves a large mass of gastroliths | |
| Heishansaurus | 1953 | Minhe Formation (Late Cretaceous, Campanian to Maastrichtian) | China | May be a junior synonym of Pinacosaurus[43] | |
| Helioceratops | 2009 | Quantou Formation (Early Cretaceous to Late Cretaceous, Albian to Cenomanian) | China | Had a distinctively short lower jaw | |
| Hexing | 2012 | Yixian Formation (Early Cretaceous, Valanginian to Barremian) | China | Toothed as evidenced by three or four preserved teeth | |
| Hexinlusaurus | 2005 | Shaximiao Formation (Middle Jurassic, Bajocian) | China | Originally named as a species of Yandusaurus | |
| Heyuannia | 2002 | Barun Goyot Formation, Dalangshan Formation (Late Cretaceous, Maastrichtian) | China Mongolia |
Fossilized pigments in referred eggshells suggest they were blue-green[44] | |
| Homalocephale | 1974 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Has been suggested to be a juvenile Prenocephale on account of its flat head,[45] but this is no longer thought to be the case[46] | |
| Huabeisaurus | 2000 | Huiquanpu Formation (Late Cretaceous, Cenomanian to Maastrichtian) | China | May be closely related to Tangvayosaurus[47] | |
| Hualianceratops | 2015 | Shishugou Formation (Late Jurassic, Oxfordian) | China | The surface of its dentary was characteristically ornamented | |
| Huanansaurus | 2015 | Nanxiong Formation (Late Cretaceous, Campanian to Maastrichtian) | China | Possessed a distinctive short trapezoidal crest | |
| Huanghetitan | 2006 | Haoling Formation, Hekou Group (Early Cretaceous, Aptian to Albian) | China | Had ribs 3 metres (9.8 ft) long, which supported the deepest body cavity of any dinosaur[48] | |
| Huangshanlong | 2014 | Hongqin Formation (Middle Jurassic, Aalenian to Callovian) | China | Known from some bones of the right forelimb | |
| Huaxiagnathus | 2004 | Yixian Formation (Early Cretaceous, Aptian) | China | One of the largest known compsognathids | |
| Huayangosaurus | 1982 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | China | A basal stegosaur that possessed flank osteoderms and a small tail club in addition to its plates and spikes | |
| Hudiesaurus | 1997 | Kalaza Formation (Late Jurassic, Tithonian) | China | Had a butterfly-shaped process on its vertebra | |
| Hulsanpes | 1982 | Barun Goyot Formation (Late Cretaceous, Campanian) | Mongolia | Closely related to Halszkaraptor but appears to be more cursorial[49] | |
| Ichthyovenator | 2012 | Grès supérieurs Formation (Early Cretaceous, Aptian) | Laos | 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) | China | Two specimens of different ontogenetic stages are known, both with differing types of feathers[50] | |
| Irisosaurus | 2020 | Fengjiahe Formation (Early Jurassic, Hettangian) | China | Closely related to Mussaurus[51] | |
| Isanosaurus | 2000 | Nam Phong Formation (Late Triassic, Norian to Rhaetian) | Thailand | May have actually come from the Late Jurassic[52] | |
| Ischioceratops | 2015 | Wangshi Group (Late Cretaceous, Campanian to Maastrichtian) | China | Noted for its peculiarly-shaped ischium | |
| Itemirus | 1976 | Bissekty Formation (Late Cretaceous, Turonian) | Uzbekistan | Originally known from a braincase but abundant new remains were described in 2014[53] | |
| Jaxartosaurus | 1937 | Dabrazhin Formation (Late Cretaceous, Santonian) | Kazakhstan | Not known from many remains but they are enough to tell that it was a basal lambeosaurine[54] | |
| Jeholosaurus | 2000 | Yixian Formation (Early Cretaceous, Aptian) | China | One specimen is preserved in a curled position | |
| Jianchangosaurus | 2013 | Yixian Formation (Early Cretaceous, Barremian) | China | Several characters of its teeth and jaws are convergently similar to those of ornithischians[55] | |
| Jiangjunosaurus | 2007 | Shishugou Formation (Late Jurassic, Oxfordian) | China | Had two rows of circular or diamond-shaped plates | |
| Jiangshanosaurus | 2001 | Jinhua Formation (Early Cretaceous, Albian) | China | A potential member of the Euhelopodidae[56] | |
| Jiangxisaurus | 2013 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | China | Overall similar to Heyuannia but with a thinner, frailer mandible | |
| Jianianhualong | 2017 | Yixian Formation (Early Cretaceous, Aptian) | China | Possessed a subtriangular tail frond made of asymmetrical feathers | |
| Jinbeisaurus | 2019 | Huiquanpu Formation (Late Cretaceous, Cenomanian to Maastrichtian) | China | Medium-sized for a tyrannosauroid | |
| Jinfengopteryx | 2005 | Huajiying Formation (Early Cretaceous, Aptian) | China | May have been capable of some sort of flight[57] | |
| Jingshanosaurus | 1995 | Lufeng Formation (Early Jurassic, Hettangian) | China | One of the latest-surviving non-sauropod sauropodomorphs | |
| Jintasaurus | 2009 | Xinminbao Group (Early Cretaceous, Albian) | China | 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) | China | The oldest ankylosaurid that preserves a tail club | |
| Jinzhousaurus | 2001 | Yixian Formation (Early Cretaceous, Aptian) | China | Its holotype is nearly complete, preserved whole on a single slab | |
| Jiutaisaurus | 2006 | Quantou Formation (Early Cretaceous to Late Cretaceous, Aptian to Cenomanian) | China | Named based on eighteen vertebrae | |
| Kaijiangosaurus | 1984 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | China | Potentially synonymous with other medium-sized Shaximiao theropods | |
| Kamuysaurus | 2019 | Hakobuchi Formation (Late Cretaceous, Maastrichtian) | Japan | Informally referred to as "Mukawaryu" before its formal description | |
| Kansaignathus | 2021 | Ialovachsk Formation (Late Cretaceous, Santonian) | Tajikistan | The first non-avian dinosaur described from Tajikistan | |
| Kazaklambia | 2013 | Dabrazhin Formation (Late Cretaceous, Santonian) | Kazakhstan | Morphologically distinct from other Eurasian lambeosaurines[58] | |
| Kelmayisaurus | 1973 | Lianmuqin Formation (Early Cretaceous, Valanginian to Albian) | China | One popular book mentions a giant species belonging to this genus,[59] but may not actually belong to this theropod | |
| Kerberosaurus | 2004 | Tsagayan Formation (Late Cretaceous, Maastrichtian) | Russia | Potentially a close relative of Edmontosaurus[60] | |
| Khaan | 2001 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | Two morphotypes of chevrons are known, which may be a sexually dimorphic trait[61] | |
| Khulsanurus | 2021 | Barun Goyot Formation (Late Cretaceous, Campanian) | Mongolia | Contemporary with Parvicursor but can be distinguished by characters of its caudal vertebrae[62] | |
| Kileskus | 2010 | Itat Formation (Middle Jurassic, Bathonian) | Russia | Uncertain if it possesses the head crest as seen in other proceratosaurids | |
| Kinnareemimus | 2009 | Sao Khua Formation (Early Cretaceous, Barremian) | Thailand | Potentially one of the oldest ornithomimosaurs | |
| Klamelisaurus | 1993 | Shishugou Formation (Middle Jurassic, Callovian) | China | Close relatives included several referred species of Mamenchisaurus[63] | |
| Kol | 2009 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | Had a "hyperarctometatarsus" more strongly pinched than other arctometatarsalian taxa. Described as an alvarezsaurid[64] but has been suggested to be related to Avimimus[65] | |
| Koreaceratops | 2011 | Tando Beds (Early Cretaceous, Albian) | South Korea | Possessed elongated neural spines on its caudal vertebrae that may have formed a swimming organ | |
| Koreanosaurus | 2011 | Seonso Conglomerate (Late Cretaceous, Santonian to Campanian) | South Korea | Had short but powerful forelimbs which may be an adaptation to digging burrows | |
| Koshisaurus | 2015 | Kitadani Formation (Early Cretaceous, Barremian) | Japan | Distinguished from other hadrosauroids by the presence of an antorbital fossa | |
| Kulceratops | 1995 | Khodzhakul Formation (Early Cretaceous, Albian) | Uzbekistan | Only known from fragments of a jaw and teeth | |
| Kulindadromeus | 2014 | Ukureyskaya Formation (Middle Jurassic, Bathonian) | Russia | An ornithischian that preserves evidence of filaments, suggesting that protofeathers were basal to Dinosauria as a whole | |
| Kundurosaurus | 2012 | Udurchukan Formation (Late Cretaceous, Maastrichtian) | Russia | May be synonymous with Kerberosaurus[66] | |
| Kuru | 2021 | Barun Goyot Formation (Late Cretaceous, Maastrichtian) | Mongolia | Had been informally referred to as "Airakoraptor" prior to its formal description | |
| Laiyangosaurus | 2017 | Wangshi Group (Late Cretaceous, Maastrichtian) | China | Some specimens referred to this edmontosaurin actually belong to kritosaurins and lambeosaurines[67] | |
| Lanzhousaurus | 2005 | Hekou Group (Early Cretaceous, Barremian) | China | Possessed the largest known teeth of any dinosaur | |
| Leshansaurus | 2009 | Shaximiao Formation (Late Jurassic, Oxfordian to Kimmeridgian) | China | Its braincase is nearly identical to that of Piveteausaurus[68] | |
| Levnesovia | 2009 | Bissekty Formation (Late Cretaceous, Turonian) | Uzbekistan | Together with Bactrosaurus and Gilmoreosaurus, it may represent an early radiation of hadrosauroids[69] | |
| Liaoceratops | 2002 | Yixian Formation (Early Cretaceous, Barremian) | China | One specimen was found without a skull roof, possibly displaced by a predator to eat its brain[70] | |
| Liaoningosaurus | 2000 | Jiufotang Formation, Yixian Formation (Early Cretaceous, Aptian) | China | May have possessed fork-like teeth and sharp claws. These and purported stomach contents containing fish may be evidence of a semi-aquatic, turtle-like lifestyle | |
| Liaoningotitan | 2018 | Yixian Formation (Early Cretaceous, Barremian) | China | The second sauropod known from the Yixian Formation | |
| Liaoningvenator | 2017 | Yixian Formation (Early Cretaceous, Barremian) | China | A troodontid with characteristically elongated legs | |
| Limusaurus | 2009 | Shishugou Formation (Late Jurassic, Oxfordian) | China | 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[71] | |
| Lingwulong | 2018 | Yanan Formation (Early Jurassic to Middle Jurassic, Toarcian to Bajocian) | China | The oldest known neosauropod and the first confirmed diplodocoid from Asia. Relatively derived despite its early age | |
| Lingyuanosaurus | 2019 | Jehol Group (Early Cretaceous, Valanginian to Aptian) | China | Possessed a mix of basal and derived therizinosaurian traits | |
| Linhenykus | 2011 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | China | Completely monodactyl due to lacking the vestigial second and third fingers of other alvarezsaurids | |
| Linheraptor | 2010 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | China | Potentially a synonym of Tsaagan[72] | |
| Linhevenator | 2011 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | China | Had a greatly enlarged sickle claw, comparable in size to those of dromaeosaurids | |
| Liubangosaurus | 2010 | Xinlong Formation (Early Cretaceous, Aptian) | China | Described only as a eusauropod[73] but may have been a somphospondylian[74] | |
| Luanchuanraptor | 2010 | Qiupa Formation (Late Cretaceous, Maastrichtian) | China | A possible member of the Velociraptorinae closely related to Adasaurus[75] | |
| Lufengosaurus | 1940 | Lufeng Formation (Early Jurassic, Hettangian to Sinemurian) | China | The rib of one specimen preserves the oldest known evidence of collagen proteins[76] | |
| Luoyanggia | 2009 | Haoling Formation (Early Cretaceous, Aptian to Albian) | China | Originally believed to date from the Late Cretaceous | |
| Machairasaurus | 2010 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | China | A potential specimen has been found brooding on its eggs[77] | |
| Mahakala | 2007 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | Possessed basal traits for a dromaeosaurid. May be a close relative of Halszkaraptor[78] | |
| Maleevus | 1987 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | Mongolia | Its only purportedly distinguishing trait is also shared with Pinacosaurus[29] | |
| Mamenchisaurus | 1954 | Penglaizhen Formation, Shaximiao Formation, Suining Formation (Late Jurassic to Early Cretaceous, Oxfordian to Aptian) | China | Several species have been named, but most may not belong to this genus[63] | |
| Mandschurosaurus | 1930 | Yuliangze Formation (Late Cretaceous, Maastrichtian) | China Laos? |
One of the first non-avian dinosaurs named from Chinese remains | |
| Mei | 2004 | Yixian Formation (Early Cretaceous, Aptian) | China | Two specimens are preserved in bird-like sleeping positions[79] | |
| Microceratus | 2008 | Ulansuhai Formation (Late Cretaceous, Turonian) | China | Originally named Microceratops, although that genus name is preoccupied by a wasp | |
| Microhadrosaurus | 1979 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | China | Reportedly an unusually small hadrosaurid | |
| Micropachycephalosaurus | 1978 | Wangshi Group (Late Cretaceous, Maastrichtian) | China | Once considered to be a pachycephalosaur, although it is now usually considered to be a ceratopsian[80] | |
| Microraptor | 2000 | Jiufotang Formation (Early Cretaceous, Aptian) | China | Known from over three hundred fossils.[81] Several are well-preserved enough to reveal fine details such as feather covering and an iridescent black coloration[82] | |
| Minotaurasaurus | 2009 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | The holotype skull was excavated illegally, which obscured its true provenance until recently | |
| Mongolosaurus | 1933 | On Gong Formation (Early Cretaceous, Aptian to Albian) | China | Known from only scant remains but has been confidently assigned to Somphospondyli in recent years[74] | |
| Mongolostegus | 2018 | Dzunbain Formation (Early Cretaceous, Aptian to Albian) | Mongolia | 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?) | China | Poorly known | |
| Monolophosaurus | 1993 | Shishugou Formation (Middle Jurassic, Bathonian to Callovian) | China | Possessed a short, rectangular crest running along the middle of the skull | |
| Mononykus | 1993 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Proposed to have an anteater-like lifestyle, using its unique forearms to break into termite mounds[83] | |
| Mosaiceratops | 2015 | Xiaguan Formation (Late Cretaceous, Turonian to Campanian) | China | Combined features of different groups of basal ceratopsians | |
| Nankangia | 2013 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | China | May have specialized in soft foods such as leaves and seeds[84] | |
| Nanningosaurus | 2007 | Unnamed formation (Late Cretaceous, Maastrichtian) | China | Potentially a basal lambeosaurine | |
| Nanshiungosaurus | 1979 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | China | Originally misidentified as a sauropod on account of its unusual pelvis | |
| Nanyangosaurus | 2000 | Xiaguan Formation (Late Cretaceous, Turonian to Campanian) | China | Completely lost the first digit of its hands | |
| Napaisaurus | 2021 | Xinlong Formation (Early Cretaceous, Aptian to Albian) | China | May be closely related to contemporary Thai iguanodonts | |
| Nebulasaurus | 2015 | Zhanghe Formation (Middle Jurassic, Aalenian to Bajocian) | China | 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) | China | Could extend its arms considerably forward due to the structure of its shoulder joint[85] | |
| Nemegtomaia | 2005 | Barun Goyot Formation, Nemegt Formation (Late Cretaceous, Campanian to Maastrichtian) | Mongolia | One specimen preserves traces of damage by skin beetles[86] | |
| Nemegtonykus | 2019 | Nemegt Formation (Late Cretaceous, Campanian to Maastrichtian) | Mongolia | The second alvarezsaurid named from the Nemegt Formation | |
| Nemegtosaurus | 1971 | Nemegt Formation (Late Cretaceous, Maastrichtian) | China? Mongolia |
Had a long, low skull similar in proportions to those of diplodocoids | |
| Ningyuansaurus | 2012 | Yixian Formation (Early Cretaceous, Aptian) | China | Preserves small oval-shaped structures in its stomach region which may be seeds | |
| Nipponosaurus | 1936 | Yezo Group (Late Cretaceous, Santonian to Campanian) | Russia | Discovered on the island of Sakhalin, which was owned by Japan in 1936 but later annexed to Russia | |
| Nomingia | 2000 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Possessed a short tail ending with a pygostyle. May be synonymous with Elmisaurus[87] | |
| Oksoko | 2020 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Its third finger was so greatly reduced that it was functionally didactyl | |
| Olorotitan | 2003 | Udurchukan Formation (Late Cretaceous, Maastrichtian) | Russia | Had a broad, hatchet-shaped crest | |
| Omeisaurus | 1939 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | China | Members of this genus are characterized by extremely elongated necks | |
| Ondogurvel | 2022 | Barun Goyot Formation (Late Cretaceous, (Campanian) | Mongolia | A small insectivorous theropod | |
| Opisthocoelicaudia | 1977 | Nemegt Formation (Late Cretaceous, Campanian to Maastrichtian) | Mongolia | Walked on its metacarpals due to its complete lack of phalanges | |
| Otogosaurus | 2004 | Unknown formation (Cretaceous?) | China | Very poorly known | |
| Oviraptor | 1924 | Djadochta Formation (Late Cretaceous, Campanian to Maastrichtian) | Mongolia | Originally mistakenly thought to be an egg-eater | |
| Pachysuchus | 1951 | Lufeng Formation (Early Jurassic, Sinemurian) | China | Considered a phytosaur from its original naming until a redescription in 2012[88] | |
| Panguraptor | 2014 | Lufeng Formation (Early Jurassic, Hettangian to Sinemurian) | China | The first definitive coelophysoid known from Asia | |
| Papiliovenator | 2021 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | China | Had a short, subtriangular skull similar to those of Early Cretaceous troodontids | |
| Parvicursor | 1996 | Barun Goyot Formation (Late Cretaceous, Campanian) | Mongolia | Small but fully mature at the time of its death | |
| Pedopenna | 2005 | Daohugou Beds (Middle Jurassic, Callovian) | China | Known from a single leg with the impressions of long, symmetrical feathers | |
| Peishansaurus | 1953 | Minhe Formation (Late Cretaceous, Santonian to Campanian) | China | Originally thought to be an ankylosaur[89] but similarities have been noted with Psittacosaurus[90] | |
| Penelopognathus | 2005 | Bayin-Gobi Formation (Early Cretaceous, Albian) | China | Named from a single dentary | |
| Phaedrolosaurus | 1973 | Lianmuqin Formation (Early Cretaceous, Valanginian to Albian) | China | May have been a dromaeosaurid[91] | |
| Philovenator | 2012 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | China | Closely related to the contemporary Linhevenator[79] but likely represents a separate taxon[92] | |
| Phuwiangosaurus | 1994 | Sao Khua Formation (Early Cretaceous, Valanginian to Hauterivian) | Thailand | A large member of the Euhelopodidae[74] | |
| Phuwiangvenator | 2019 | Sao Khua Formation) (Early Cretaceous, Barremian) | Thailand | Potentially the most basal megaraptoran[93] | |
| Pinacosaurus | 1933 | Bayan Mandahu Formation, Djadochta Formation (Late Cretaceous, Campanian) | China Mongolia |
Possessed an enlarged hyoid that may indicate a feeding specialization such as fruit-eating or anteater-like insectivory[94] | |
| Plesiohadros | 2014 | Alagteeg Formation (Late Cretaceous, Campanian) | Mongolia | The largest animal from the Djadochta area | |
| Prenocephale | 1974 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Had a distinctively conical dome | |
| Probactrosaurus | 1966 | Dashuigou Formation (Late Cretaceous, Cenomanian to Coniacian) | China | The closest relative to the Hadrosauromorpha based on the definition of the group[95] | |
| Prodeinodon | 1924 | Öösh Formation, Xinlong Formation (Early Cretaceous, Barremian to Aptian) | China Mongolia |
Potentially a carnosaur[96] | |
| Protarchaeopteryx | 1997 | Yixian Formation (Early Cretaceous, Aptian) | China | Usually thought to be a basal oviraptorosaur but one study suggests a basal position within Pennaraptora[75] | |
| Protoceratops | 1923 | Bayan Mandahu Formation, Djadochta Formation (Late Cretaceous, Campanian) | China Mongolia |
Its remains are so abundant that it has been nicknamed the "sheep of the Cretaceous" | |
| Protognathosaurus | 1991 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | China | Originally Protognathus, that name was preoccupied by a Carabidae genus, Protognathus Basilewsky, 1950[97] (Syn. for accepted name: Pseudognathaphanus Schauberger, 1932.) | |
| 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) | China Mongolia Russia Thailand |
Known from hundreds of specimens, many of them well-preserved. Lived in a broad range | |
| Pukyongosaurus | 2001 | Hasandong Formation (Early Cretaceous, Aptian to Albian) | South Korea | One of its caudal vertebrae has bite marks caused by theropod teeth | |
| Qianzhousaurus | 2014 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | China | Has been nicknamed "Pinocchio rex" on account of its elongated snout | |
| Qiaowanlong | 2009 | Xinminbao Group (Early Cretaceous, Albian) | China | Originally described as a brachiosaurid[98] but has since been reinterpreted as a euhelopodid[99] | |
| Qijianglong | 2015 | Suining Formation (Early Cretaceous, Aptian) | China | Once believed to date from the Late Jurassic | |
| Qingxiusaurus | 2008 | Unnamed formation (Late Cretaceous, Maastrichtian) | China | Known from very limited remains | |
| Qinlingosaurus | 1996 | Hongtuling Formation (Late Cretaceous, Maastrichtian) | China | Potentially a titanosaur given its age, but this cannot be confirmed | |
| Qiupalong | 2011 | Qiupa Formation (Late Cretaceous, Campanian to Maastrichtian) | China | A referred specimen was found in Canada[100] | |
| Qiupanykus | 2018 | Qiupa Formation (Late Cretaceous, Maastrichtian) | China | May have used its robust thumb claws to crack open oviraptorid eggshells[101] | |
| Quaesitosaurus | 1983 | Nemegt Formation (Late Cretaceous, Santonian to Maastrichtian} | Mongolia | Potentially a close relative of Nemegtosaurus | |
| Ratchasimasaurus | 2011 | Khok Kruat Formation (Early Cretaceous, Aptian) | Thailand | Indeterminate compared to other styracosternans | |
| Rhomaleopakhus | 2021 | Kalaza Formation (Late Jurassic, Tithonian) | China | Possessed a robust forelimb that may be a locomotory adaptation | |
| Rinchenia | 2004 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Had a tall, domed crest | |
| Ruyangosaurus | 2009 | Haoling Formation (Early Cretaceous, Aptian to Albian) | China | Only known from scant remains but was one of the largest dinosaurs known from Asia | |
| Sahaliyania | 2008 | Yuliangze Formation (Late Cretaceous, Maastrichtian) | China | Known from a bonebed where eighty percent of the remains are from this taxon[102] | |
| Saichania | 1977 | Barun Goyot Formation, Nemegt Formation (Late Cretaceous, Campanian to Maastrichtian) | Mongolia | Possessed complicated nasal passages that may have cooled the air it breathed | |
| Sanpasaurus | 1944 | Ziliujing Formation (Early Jurassic, Toarcian) | China | Historically conflated with the remains of an ornithischian | |
| Sanxiasaurus | 2019 | Xintiangou Formation (Middle Jurassic, Bajocian | China | The oldest neornithischian known from Asia | |
| Saurolophus | 1912 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | 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) | China | Preserved lying on its back with parts of its armor in an articulated position | |
| Saurornithoides | 1924 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | Very bird-like in the construction of its bones | |
| Scansoriopteryx | 2002 | Daohugou Beds (Middle Jurassic, Callovian) | China | Was well-adapted for climbing due to the structure of its hands and feet | |
| Segnosaurus | 1979 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Turonian) | Mongolia | One of the first known therizinosaurs. Its relationships were originally obscure | |
| Serikornis | 2017 | Tiaojishan Formation (Middle Jurassic, Callovian) | China | Possessed simple, wispy feathers similar to those of a Silkie chicken | |
| Shamosaurus | 1983 | Dzunbain Formation (Early Cretaceous, Aptian to Albian) | Mongolia | Had a flat, narrow skull | |
| Shanag | 2007 | Öösh Formation (Early Cretaceous, Berriasian to Barremian) | Mongolia | Shows a mixture of traits of various paravian groups | |
| Shantungosaurus | 1973 | Hongtuya Formation, Xingezhuang Formation (Late Cretaceous, Campanian) | China | The largest known hadrosaurid | |
| Shanxia | 1998 | Huiquanpu Formation (Late Cretaceous, Cenomanian to Campanian) | China | May be synonymous with Tianzhenosaurus[103] and/or Saichania[29] | |
| Shanyangosaurus | 1996 | Shanyang Formation (Late Cretaceous, Maastrichtian) | China | Indeterminate but its hollow bones are a synapomorphy for Coelurosauria. One study suggests an oviraptorosaurian position[75] | |
| Shaochilong | 2009 | Ulansuhai Formation (Late Cretaceous, Turonian) | China | Had a relatively short maxilla | |
| Shenzhousaurus | 2003 | Yixian Formation (Early Cretaceous, Aptian) | China | Preserves pebbles in its thoracic cavity which may be gastroliths | |
| Shidaisaurus | 2009 | Chuanjie Formation (Middle Jurassic, Aalenian) | China | Potentially one of the oldest known allosauroids | |
| Shishugounykus | 2019 | Shishugou Formation (Late Jurassic, Oxfordian) | China | Its manus combines features of both alvarezsaurians and more basal coelurosaurs | |
| Shixinggia | 2005 | Pingling Formation (Late Cretaceous, Maastrichtian) | China | Known from some postcranial material | |
| Shri | 2021 | Barun Goyot Formation (Late Cretaceous, Maastrichtian) | Mongolia | Before its formal description, it was nicknamed "Ichabodcraniosaurus" because its holotype lacked a skull | |
| Shuangmiaosaurus | 2003 | Sunjiawan Formation (Early Cretaceous, Albian) | China | Only known from some parts of a skull | |
| Shunosaurus | 1983 | Shaximiao Formation (Late Jurassic, Oxfordian) | China | Possessed a small tail club topped by two short spikes | |
| Shuvuuia | 1998 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | May have been a nocturnal, owl-like hunter[104] | |
| Siamodon | 2011 | Khok Kruat Formation (Early Cretaceous, Aptian) | Thailand | May have been closely related to Probactrosaurus[105] | |
| Siamosaurus | 1986 | Khok Kruat Formation, Sao Khua Formation (Early Cretaceous, Barremian to Aptian) | Thailand | Only known from teeth. Some spinosaurid postcrania from the same area may be referrable to this genus[106] | |
| Siamotyrannus | 1996 | Sao Khua Formation (Early Cretaceous, Berriasian to Barremian) | Thailand | Originally described as a tyrannosaurid[107] but it may in fact be a metriacanthosaurid[68] | |
| Siamraptor | 2019 | Khok Kruat Formation (Early Cretaceous, Aptian) | Thailand | Known from scattered remains, including parts of a skull | |
| Sibirotitan | 2017 | Ilek Formation (Early Cretaceous, Barremian) | Russia | Its sacral ribs are star-shaped in dorsal view | |
| Siluosaurus | 1997 | Xinminbao Group (Early Cretaceous, Barremian to Albian) | China | Possessed the smallest known teeth of any ornithopod | |
| Silutitan | 2021 | Shengjinkou Formation (Early Cretaceous, Aptian) | China | Known from six cervical vertebrae associated with a pterosaur jaw | |
| Similicaudipteryx | 2008 | Jiufotang Formation (Early Cretaceous, Aptian) | China | Had a short tail ending with a dagger-shapped pygostyle | |
| Sinankylosaurus | 2020 | Wangshi Group (Late Cretaceous, Campanian) | China | Only known from an ilium but can be identified as an ankylosaur | |
| Sinocalliopteryx | 2007 | Yixian Formation (Early Cretaceous, Barremian to Aptian) | China | Stomach contents indicate a possible preference for volant prey such as dromaeosaurids and early birds[108] | |
| Sinocephale | 2021 | Ulansuhai Formation (Late Cretaceous, Turonian) | China | Originally named as a species of Troodon when that genus was thought to be a pachycephalosaur | |
| Sinoceratops | 2010 | Xingezhuang Formation (Late Cretaceous, Campanian to Maastrichtian) | China | Possessed forward-curving hornlets and a series of low knobs on the top of the frill | |
| Sinocoelurus | 1942 | Kuangyuan Series (Late Jurassic, Oxfordian to Tithonian | China | One study considered it to be a potential plesiosaur[109] | |
| Sinornithoides | 1993 | Ejinhoro Formation (Early Cretaceous, Aptian to Albian) | China | Preserved in a roosting position, its head tucked underneath its left wing | |
| Sinornithomimus | 2003 | Ulansuhai Formation (Late Cretaceous, Turonian) | China | Formed age-segregated herds as evidenced by a concentration of juvenile skeletons[110] | |
| Sinornithosaurus | 1999 | Yixian Formation (Early Cretaceous, Aptian) | China | One specimen has disloged teeth, leading to suggestions it was venomous[111] | |
| Sinosauropteryx | 1996 | Yixian Formation (Early Cretaceous, Aptian) | China | The first non-avian dinosaur found with direct evidence of feathers. Analysis of melanosomes suggest it had orange-brown and white countershading with a striped tail and a "bandit mask" around its eyes[112] | |
| Sinosaurus | 1940 | Lufeng Formation (Early Jurassic, Hettangian to Sinemurian) | China | Had a pair of midline crests similar to Dilophosaurus | |
| Sinotyrannus | 2009 | Jiufotang Formation (Early Cretaceous, Aptian) | China | One of the earliest known large tyrannosauroids. Closely related to smaller forms such as Proceratosaurus and Guanlong | |
| Sinovenator | 2002 | Yixian Formation (Early Cretaceous, Aptian) | China | Some specimens are preserved three-dimensionally | |
| Sinraptor | 1994 | Shishugou Formation (Late Jurassic, Oxfordian) | China | May have used its teeth like blades to inflict deep wounds in prey | |
| Sinusonasus | 2004 | Yixian Formation (Early Cretaceous, Hauterivian) | China | Had distinctive sinusoid nasal bones | |
| Sirindhorna | 2015 | Khok Kruat Formation (Early Cretaceous, Aptian) | Thailand | Discovered by corn farmers while digging a reservoir | |
| Sonidosaurus | 2009 | Iren Dabasu Formation (Late Cretaceous, Cenomanian to Campanian) | China | Unusually, its ilium was not pneumatic | |
| Stegosaurides | 1953 | Xinminbao Group (Early Cretaceous, Barremian to Albian) | China | A thyreophoran of uncertain phylogenetic position | |
| Suzhousaurus | 2007 | Xinminbao Group (Early Cretaceous, Aptian to Albian) | China | Had a large ilium which is markedly broad on the anterior end | |
| Szechuanosaurus | 1942 | Shaximiao Formation (Late Jurassic, Oxfordian to Tithonian) | China | Only known from teeth and a very fragmentary skeleton | |
| Talarurus | 1952 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | Mongolia | Its tail club has been compared to a wicker basket | |
| Tambatitanis | 2014 | Sasayama Group (Early Cretaceous, Albian) | Japan | Possessed disproportionately large chevrons | |
| Tangvayosaurus | 1999 | Grès supérieurs Formation (Early Cretaceous, Aptian to Albian) | Laos | Closely related to Phuwiangosaurus | |
| Tanius | 1929 | Jiangjunding Formation (Late Cretaceous, Campanian to Maastrichtian) | China | Today known from only a few bones; more fossils were once present but were not collected | |
| Taohelong | 2013 | Hekou Group (Early Cretaceous, Albian) | China | Possessed a sacral shield similar to that of Polacanthus | |
| Tarbosaurus | 1955 | Nemegt Formation, Subashi Formation (Late Cretaceous, Maastrichtian) | China Mongolia |
An apex predator that hunted large prey. Very similar to Tyrannosaurus | |
| Tarchia | 1977 | Barun Goyot Formation, Nemegt Formation (Late Cretaceous, Campanian to Maastrichtian) | Mongolia | One specimen preserves injuries to its ribs and tail, possibly from a fight with a member of its own kind[113] | |
| Tatisaurus | 1965 | Lufeng Formation (Early Jurassic, Sinemurian) | China | Potentially a basal thyreophoran | |
| Tengrisaurus | 2017 | Murtoi Formation (Early Cretaceous, Barremian to Aptian) | Russia | Closely related to South American titanosaurs | |
| Therizinosaurus | 1954 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Possessed extremely elongated and stiffened hand claws | |
| Tianchisaurus | 1993 | Toutunhe Formation (Middle Jurassic, Bajocian to Bathonian) | China | Its description uses the spellings Tianchisaurus and Tianchiasaurus interchangeably, but the former is correct[114] | |
| Tianyulong | 2009 | Tiaojishan Formation (Late Jurassic, Oxfordian) | China | Preserves impressions of long bristles down its back, tail and neck | |
| Tianyuraptor | 2009 | Yixian Formation (Early Cretaceous, Barremian to Aptian) | China | Combines features of both northern and southern dromaeosaurids. Had unusual proportions | |
| Tianzhenosaurus | 1998 | Huiquanpu Formation (Late Cretaceous, Cenomanian to Campanian) | China | May be synonymous with Saichania[29] | |
| Tienshanosaurus | 1937 | Shishugou Formation (Late Jurassic, Oxfordian) | China | Large but basal for a mamenchisaurid[63] | |
| Timurlengia | 2016 | Bissekty Formation (Late Cretaceous, Turonian) | Uzbekistan | Its inner ear was specialized for detecting low-frequency sounds[115] | |
| Tochisaurus | 1991 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Known from only a single metatarsus | |
| Tonganosaurus | 2010 | Yimen Formation (Early Jurassic, Pliensbachian) | China | Potentially the oldest known mamenchisaurid | |
| Tongtianlong | 2016 | Nanxiong Formation (Late Cretaceous, Maastrichtian) | China | The pose of the holotype suggests it died while trying to free itself from mud | |
| Tsaagan | 2006 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | Very similar to Velociraptor but differs in some features of the skull[116] | |
| Tsagantegia | 1993 | Bayan Shireh Formation (Late Cretaceous, Cenomanian to Santonian) | Mongolia | Had a long, shovel-shaped snout which may indicate a browsing lifestyle[117] | |
| Tsintaosaurus | 1958 | Jingangkou Formation (Late Cretaceous, Campanian) | China | Originally mistakenly believed to have possessed a unicorn horn-like crest | |
| Tugulusaurus | 1973 | Lianmuqin Formation (Early Cretaceous, Barremian to Albian) | China | Potentially an early, Xiyunykus-grade alvarezsaurian[118] | |
| Tuojiangosaurus | 1977 | Shaximiao Formation (Late Jurassic, Oxfordian to Kimmeridgian) | China | Possessed seventeen pairs of tall, pointed plates, thickened in the center as if they were modified spikes | |
| Turanoceratops | 1989 | Bissekty Formation (Late Cretaceous, Turonian) | Uzbekistan | Had a pair of brow horns like ceratopsids but was likely not a member of that family | |
| Tylocephale | 1974 | Barun Goyot Formation (Late Cretaceous, Campanian) | Mongolia | Known from a partial skull but it is enough to tell that it had a remarkably tall dome | |
| Udanoceratops | 1992 | Djadochta Formation (Late Cretaceous, Campanian) | Mongolia | The largest known leptoceratopsid | |
| Ultrasaurus | 1983 | Gugyedong Formation (Early Cretaceous, Aptian to Albian) | South Korea | Described as very large but this may be due to misidentification of a bone | |
| Ulughbegsaurus | 2021 | Bissekty Formation (Late Cretaceous, Turonian) | Uzbekistan | A very large and late-surviving carnosaur | |
| Urbacodon | 2007 | Bissekty Formation, Dzharakuduk Formation (Late Cretaceous, Cenomanian to Turonian) | Uzbekistan | The holotype preserves a gap separating the eight rear teeth from the rest of its teeth | |
| Vayuraptor | 2019 | Sao Khua Formation (Early Cretaceous, Barremian) | Thailand | Potentially ancestral to megaraptorans[93] | |
| Velociraptor | 1924 | Bayan Mandahu Formation, Djadochta Formation (Late Cretaceous, Campanian) | China Mongolia |
Quill knobs preserved on an ulna conclusively prove it had feathers[119] | |
| Wakinosaurus | 1992 | Sengoku Formation (Early Cretaceous, Hauterivian to Barremian) | Japan | May be a close relative of Acrocanthosaurus[96] | |
| Wannanosaurus | 1977 | Xiaoyan Formation (Late Cretaceous Campanian to Maastrichtian) | China | Basal for a pachycephalosaur as indicated by its flat skull with large openings | |
| Wuerhosaurus | 1973 | Ejinhoro Formation, Tugulu Group (Early Cretaceous, Hauterivian) | China | One of the last and largest known stegosaurs. Preserved with low rectangular plates but these may be broken | |
| Wulagasaurus | 2008 | Yuliangze Formation (Late Cretaceous, Maastrichtian) | China | A rare hadrosaurid known from far less remains than the contemporary Sahaliyania | |
| Wulatelong | 2013 | Bayan Mandahu Formation (Late Cretaceous, Campanian) | China | Known from a partial skeleton including some parts of the skull | |
| Wulong | 2020 | Jiufotang Formation (Early Cretaceous, Aptian) | China | Possessed an extremely long tail tipped by two long feathers | |
| Xianshanosaurus | 2009 | Haoling Formation (Early Cretaceous, Albian) | China | May have been closely related to Daxiatitan[74] | |
| Xiaosaurus | 1983 | Shaximiao Formation (Middle Jurassic, Bajocian to Callovian) | China | An ornithischian of uncertain affinities | |
| Xiaotingia | 2011 | Tiaojishan Formation (Late Jurassic, Oxfordian) | China | Well-preserved but inconsistent in phylogenetic placement. Some studies suggest a position as an early avialan[120] | |
| Xingtianosaurus | 2019 | Yixian Formation (Early Cretaceous, Aptian) | China | Retained the large third finger that was lost in other caudipterids | |
| Xingxiulong | 2017 | Lufeng Formation (Early Jurassic, Hettangian | China | Possessed a robust scapula which increased forelimb mobility for feeding | |
| Xinjiangovenator | 2005 | Lianmuqin Formation (Early Cretaceous, Valanginian to Albian) | China | Remains originally identified as Phaedrolosaurus | |
| Xinjiangtitan | 2013 | Qiketai Formation (Middle Jurassic, Callovian) | China | Had an extremely long neck | |
| Xiongguanlong | 2009 | Xiagou Formation, (Early Cretaceous, Aptian to Albian) | China | Robust with a long snout and strong vertebrae | |
| Xixianykus | 2010 | Majiacun Formation (Late Cretaceous, Santonian to Campanian) | China | One of the smallest known non-avian dinosaurs | |
| Xixiasaurus | 2010 | Majiacun Formation (Late Cretaceous, Coniacian to Campanian) | China | Distinguished from other troodontids by its possession of exactly twenty-two teeth in each maxilla | |
| Xixiposaurus | 2010 | Lufeng Formation (Early Jurassic, Hettangian to Pliensbachian) | China | Poorly known | |
| Xiyunykus | 2018 | Tugulu Group (Early Cretaceous, Barremian to Aptian) | China | Had an unspecialized hand morphology for an alvarezsaur, having three fingers of roughly equal length and construction | |
| Xuanhanosaurus | 1984 | Shaximiao Formation (Middle Jurassic, Bathonian to Callovian) | China | Originally mistakenly believed to have been capable of quadrupedal locomotion | |
| Xuanhuaceratops | 2006 | Houcheng Formation (Late Jurassic, Tithonian) | China | Possessed a large premaxillary tooth right behind its beak | |
| Xunmenglong | 2019 | Huajiying Formation (Early Cretaceous, Hauterivian) | China | The holotype was originally presented as part of a chimera involving three different animals[121] | |
| Xuwulong | 2011 | Xinminbao Group (Early Cretaceous, Aptian to Albian) | China | The tip of its dentary was V-shaped when viewed from the side | |
| Yamaceratops | 2006 | Javkhlant Formation (Late Cretaceous, Santonian) | Mongolia | Possessed a short, stubby frill | |
| Yamatosaurus | 2021 | Kita-Ama Formation (Late Cretaceous, Maastrichtian) | Japan | Basal yet survived late enough to be contemporaneous with more advanced hadrosaurids | |
| Yandusaurus | 1979 | Shaximiao Formation (Middle Jurassic, Bathonian) | China | Some fossils were destroyed by a composter before they could be studied[122] | |
| Yangchuanosaurus | 1978 | Shaximiao Formation (Late Jurassic, Oxfordian) | China | The largest theropod known from the Shaximiao | |
| Yi | 2015 | Tiaojishan Formation (Late Jurassic, Oxfordian) | China | Preserves impressions of both feathers and a membranous wing | |
| Yimenosaurus | 1990 | Fengjiahe Formation (Early Jurassic, Pliensbachian) | China | Much of its skeleton is known, including most of its skull | |
| Yingshanosaurus | 1994 | Shaximiao Formation (Late Jurassic, Kimmeridgian) | China | Possessed greatly enlarged shoulder spines | |
| Yinlong | 2006 | Shishugou Formation (Late Jurassic, Oxfordian) | China | Its skull displays features of ceratopsians, pachycephalosaurs, and heterodontosaurids | |
| Yixianosaurus | 2003 | Yixian Formation (Early Cretaceous, Aptian) | China | Inconsistent in phylogenetic placement. Had extremely elongated manual elements | |
| Yizhousaurus | 2018 | Fengjiahe Formation (Early Jurassic, Sinemurian) | China | Preserves a complete skull and lower jaw | |
| Yongjinglong | 2014 | Hekou Group (Early Cretaceous, Albian) | China | Possessed a long, broad scapula half the length of its trunk | |
| Yuanmousaurus | 2006 | Zhanghe Formation (Middle Jurassic, Aalenian to Callovian) | China | Shares features of its vertebrae with Patagosaurus | |
| Yueosaurus | 2012 | Liangtoutang Formation (Early Cretaceous to Late Cretaceous, Albian to Cenomanian) | China | Probably closely related to Jeholosaurus[123] | |
| Yulong | 2013 | Qiupa Formation (Late Cretaceous, Maastrichtian) | China | Known from five juvenile specimens, as well as an embryo and associated nest | |
| Yunganglong | 2013 | Zhumapu Formation (Late Cretaceous, Cenomanian) | China | Discovered 50 kilometres (31 mi) away from a World Heritage Site | |
| Yunmenglong | 2013 | Haoling Formation (Early Cretaceous, Aptian to Albian) | China | May have been exceptionally large | |
| Yunnanosaurus | 1942 | Fengjiahe Formation, Lufeng Formation, Zhanghe Formation (Early Jurassic to Middle Jurassic, Pliensbachian to Bajocian) | China | Its teeth were self-sharpening similar to those of sauropods, likely through convergent evolution[124] | |
| Yunyangosaurus | 2020 | Xintiangou Formation (Middle Jurassic, Aalenian) | China | Potentially an early megalosauroid | |
| Yutyrannus | 2012 | Yixian Formation (Early Cretaceous, Aptian) | China | The largest known dinosaur that preserves direct evidence of feathers | |
| Zanabazar | 2009 | Nemegt Formation (Late Cretaceous, Maastrichtian) | Mongolia | Originally named as a species of Saurornithoides. A large troodontid | |
| Zaraapelta | 2014 | Barun Goyot Formation (Late Cretaceous, Campanian) | Mongolia | Had an intricate pattern of osteoderms on its skull | |
| Zhanghenglong | 2014 | Majiacun Formation (Late Cretaceous, Santonian) | China | Reconstructed by its describers with a straight, rectangular back[125] | |
| Zhejiangosaurus | 2007 | Chaochuan Formation (Late Cretaceous, Cenomanian) | China | Has no diagnostic features[29] | |
| Zhenyuanlong | 2015 | Yixian Formation (Early Cretaceous, Aptian) | China | Possessed large wings with long feathers, but was most likely flightless | |
| Zhongjianosaurus | 2017 | Yixian Formation (Early Cretaceous, Aptian) | China | Distinguishable by its characteristically elongated legs. Described as a microraptorian[126] but one study suggests an avialan position[127] | |
| Zhuchengceratops | 2010 | Wangshi Group (Late Cretaceous, Maastrichtian) | China | Had a deep mandible | |
| Zhuchengtitan | 2017 | Wangshi Group (Late Cretaceous, Campanian) | China | The proportions of its humerus suggest a close relationship with Opisthocoelicaudia[128] | |
| Zhuchengtyrannus | 2011 | Xingezhuang Formation (Late Cretaceous, Campanian) | China | Closely related to Tarbosaurus and Tyrannosaurus | |
| Zigongosaurus | 1976 | Shaximiao Formation (Middle Jurassic to Late Jurassic, Bathonian to Tithonian) | China | May be a species of Mamenchisaurus[129] | |
| Zizhongosaurus | 1983 | Ziliujing Formation (Early Jurassic, Toarcian) | China | Poorly known but was most likely basal for a sauropod | |
| Zuolong | 2010 | Shishugou Formation (Late Jurassic, Oxfordian | China | One of the oldest coelurosaurs known from both cranial and postcranial remains | |
| Zuoyunlong | 2017 | Zhumapu Formation (Late Cretaceous, Cenomanian) | China | May have been close to the separation between North American and Asian hadrosauroids[130] |
This is a timeline of selected dinosaurs from the list above. Time is measured in Ma, megaannum, along the x-axis.

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Lists of dinosaurs by continent | ||
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| Non-avian dinosaurs |
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| Birds | ||