List of years in paleontology (table) |
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… 1991 . 1992 . 1993 . 1994 . 1995 . 1996 . 1997 … 1998 1999 2000 -2001- 2002 2003 2004 … 2005 . 2006 . 2007 . 2008 . 2009 . 2010 . 2011 … In science: 1998 1999 2000 -2001- 2002 2003 2004 |
Related time period or subjects |
… 1998 . 1999 . 2000 - 2001 - 2002 . 2003 . 2004 … … 1970s . 1980s . 1990s -2000s- 2010s . 2020s . 2030s |
Art . Archaeology . Architecture . Literature . Music . Science +... |
Paleontology, palaeontology or palæontology (from Greek: paleo, "ancient"; ontos, "being"; and logos, "knowledge") is the study of prehistoric life forms on Earth through the examination of plant and animal fossils.[1] This includes the study of body fossils, tracks (ichnites), burrows, cast-off parts, fossilised faeces (coprolites), palynomorphs and chemical residues. Because mankind has encountered fossils for millennia, paleontology has a long history both before and after becoming formalized as a science. This article records significant discoveries and events related to paleontology that occurred in the year 2001.
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Name | Status | Authors | Age | Unit | Location | Notes | Images |
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Early Devonian |
The type species is Achoania jarvikii. |
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Early Devonian |
Bear Rock Formation |
A new genus for "Speonesydrion" lehmanni. |
Name | Status | Authors | Age | Unit | Location | Notes | Images |
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Late Jurassic |
The type species is Mesophryne beipiaoensis. |
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Upper Cretaceous |
The type species is Nezpercius dodsoni. |
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Late Jurassic |
Zhangjiakou Formation |
The type species is Sinerpeton fengshanensis. |
Name | Status | Authors | Age | Unit | Location | Notes | Images |
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Upper Jurassic |
The type species is Caribemys oxfordiensis. |
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Early Cretaceous |
The type species is Cearachelys placidoi. |
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Late Cretaceous |
Kallamedu Formation |
The type species is Kurmademys kallamedensis. |
Name | Status | Authors | Age | Unit | Location | Notes | Images |
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Synonymy |
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Late Triassic |
A new genus for "Shastasaurus" neoscapularis. A junior synonymy of Callawayia Maisch & Matzke, 2000. |
Name | Status | Authors | Age | Unit | Location | Notes | Images |
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Late Triassic |
The type species is Hypuronector limnaios. |
Name | Status | Authors | Age | Unit | Location | Notes | Images |
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Lower Jurassic |
Posidonia Shale Formation |
The type species is Hauffiosaurus zanoni. |
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Early Jurassic |
The type species is Godavarisaurus latefi. |
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Rebbanasaurus[14] |
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Early Jurassic |
The type species is Rebbanasaurus jani. |
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Upper Triassic |
Tongchuan Formation |
The type species is Yonghesuchus sangbiensis. |
Name | Status | Authors | Age | Unit | Location | Notes | Images |
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Upper Cretaceous |
The type species is Pabwehshi pakistanensis. |
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Lower Cretaceous |
?Nenjiang Formation |
The type species is Rugosuchus nonganensis. |
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Upper Cretaceous |
The type species is Stratiotosuchus maxhechti. |
Data courtesy of George Olshevsky's dinosaur genera list[19] and Dr. Jeremy Montague's dinosaur genus database.[20]
Name | Status | Authors | Discovery year | Age | Unit | Location | Notes | Images |
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"Alashansaurus"[21] | Nomen ex dissertatione |
Daniel Chure |
Would later be formally named Shaochilong in 2009. |
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Valid taxon |
Ford |
A 20-foot-long (6.1 m) ankylosaurid. Apparently, before being fossilized, the animal's bloated carcass had floated out to sea and formed a miniature reef environment after it sunk to the bottom. |
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Bienosaurus[23] | Valid taxon |
A primitive scelidosaurid known from scant remains. |
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Cedarpelta[24] | Valid taxon |
The most basal known ankylosaurid. |
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Citipati[25] | Valid taxon |
James M. Clark |
A relatively large oviraptorid known to brood its nests. |
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Draconyx[26] | Valid taxon |
Octávio Mateus |
A relative of Camptosaurus. |
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Eotyrannus[27] | Valid taxon |
Hutt |
A twenty foot tyrannosauroid. |
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Eshanosaurus[28] | Valid taxon |
Xu Xing |
A therizinosauroid and possibly the earliest known coelurosaur. |
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Gobisaurus[29] | Valid taxon |
Matthew K. Vickaryous |
An ankylosaurid that resembled Shamosaurus. |
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“Hanwulosaurus”[30] | Nomen nudum |
A thirty foot ankylosaur. |
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"Heilongjiangosaurus"[31] | Nomen nudum |
Li W. |
A hadrosaur, possibly synonymous with Charonosaurus. |
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Hesperosaurus[32] | Valid taxon |
Kenneth Carpenter |
A stegosaurid slightly older and more primitive than Stegosaurus, although the genera may be synonymous. |
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Jiangshanosaurus[33] | Valid taxon |
Tang F. |
A titanosaur known only from a partial skeleton found near Lixian Village, China. |
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Jinzhousaurus[34] | Valid taxon |
Wang X. |
A hadrosauroid known from a nearly complete skeleton. |
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Khaan[25] | Valid taxon |
James M. Clark |
A fairly typical oviraptorid once misidentified as Ingenia. |
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"Kittysaurus" | Junior synonym of Eotyrannus |
Hargreaves |
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Liaoningosaurus[35] | Valid taxon |
Xu Xing |
A bizarre ankylosaur of uncertain classification. Known from the complete specimen of a juvenile 34 cm long, it's the smallest known ankylosaur to date. |
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Losillasaurus[36] | Valid taxon |
Maria Lourdes Casanovas-Cladellas |
A large turiasaur known from a partial subadult skeleton. |
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Masiakasaurus[37] | Valid taxon |
Sampson |
A 2 meter (about 6–7 feet) noasaurid with unusual forward-pointing teeth. |
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Megapnosaurus[38] | Same as Syntarsus. |
Ivie |
Formerly known as Syntarsus, this new name was erected by entomologists due to synonymy between the dinosaur and a genus of beetle. |
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Neimongosaurus[39] | Valid taxon |
A therizinosaur about 2.3 meters in length. |
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Nothronychus[40] | Valid taxon |
James Kirkland Wolfe |
A therizinosaur. |
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Paralititan[41] | Valid taxon |
J. B. Smith |
A titanosaur and of the most massive dinosaurs ever discovered, with an estimated weight of 59 tonnes (65 short tons) and length of around 26 meters (85 ft). |
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Planicoxa[42] | Valid taxon |
DiCroce |
An advanced iguanodontian. |
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Pukyongosaurus[43] | Valid taxon |
Dong Zhiming |
A titanosauriform related to Euhelopus. |
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Quilmesaurus[44] | Valid taxon |
A 5–6 meter (16–20 feet) theropod known from a partial leg. |
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Rapetosaurus[45] | Valid taxon |
Kristina Curry-Rogers |
A 15 metres (49 ft) titanosaur. |
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Ruehleia[46] | Valid taxon |
A prosauropod named for Hugo Ruehle von Lilienstern. |
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"Szechuanoraptor"[21] | Nomen ex dissertatione |
Daniel Chure |
A theropod not yet formally described. The name was coined by Daniel Chure in 2000. |
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Valid non-dinosaurian taxon. |
Very similar to Archaeopteryx, which may be its senior synonym. |
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Venenosaurus[48] | Valid taxon |
Tidwell |
A relatively small (probably around 10 m (33 ft) long) titanosauriform sauropod, known from an incomplete skeleton of an adult and a juvenile. Its tail vertebrae articulated in a unique fashion that may be of evolutionary significance. |
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"Yibinosaurus"[49] | Nomen nudum |
Ouyang vide: Anonymous |
A saropod from Szechuan slated to be described by Ouyang Hui. |
Laelaps trihedrodon was one of the many species described by Edward Drinker Cope that he referred to his preoccupied genus Laelaps, later renamed Dryptosaurus. Although the type specimen included a partial dentary, all material except for a collection of five damaged partial tooth crowns (AMNH 5780) has been lost.[50] The rediscovered material had lately been mistaken by Mcintosh for the type specimen in 1998. However this identification was impossible because the type's teeth were described by Cope as "smooth" and having a "fine silky luster," while the AMNH 5780 teeth were thoroughly worn and had matrix clinging to them. Most of the type specimen's teeth were successional, but all the AMNH 5780 teeth were functional.[51] AMNH 5780 has many features in common with Allosaurus and is probably referrable to that genus. However some of the Allosaurus-like characters of the tooth are primitive to theropods as a whole and may have been present in the less studied or poorly preserved Morrison theropod species. Consequently the synonymization of L. trihedrodon with Allosaurus is tentative, despite its high likelihood.[52]
Hans C. E. Larsson published a description of the inner ear and endocranium of Carcharodontosaurus saharicus.[53] The C. saharicus braincase "completely encloses the endocranial region." This "high degree of ossification" made detailed analysis of its anatomy significantly easier.[54] The C. saharicus endocast is similar to that of a related dinosaur, Allosaurus fragilis. Larsson describes the olfactory bulbs and peduncles as lying "on approximately the same horizontal plane as the forebrain." The cephalic flexure, the bend between the fore- and midbrain, has an angle of 45 degrees. The pontine flexure, the bend between the mid- and hindbrain has an angle of about 40 degrees. Carcharodontosaurus had a large optic (II) nerve. The C. saharicus vena capitis dorsalis" drains the anterior neck muscles through a pair of long canals on the posterior surface of the endocast." Allosaurus, Dromaeosaurus albertensis, although in C. saharicus and Troodon "the transverse sinus probably drained into a middle cerebral vein that exited the brain in the ridge present on the dorsal edge of the trigeminal foramen."
The three semicircular canals of the inner ear of Carcharodontosaurus saharicus, when viewed from the side, had a subtriangular outline. This subtriangular inner ear configuration is present in Allosaurus, lizards, turtles, but not in birds. The pointed apex "at the junction of the anterior and posterior semicircular canals" is caused by the near linearity of the canals and closely resembles the condition of modern crocodiles. The subtriangular configuration may be the basal condition of archosauromorphs. A recess which would have held the floccular lobe of the brain projects into the area surrounded by the semicircular canals. This condition is also present in other non-avian theropods, birds, and pterosaurs. The orientation of the lagena of C. saharicus resembles the condition in crocodillians and some birds. The extent of its perilymphatic duct resembled those of Varanus, crocodillians, and birds. The crista which would have supported the secondary tympanic membrane in C. saharicus was either absent, or not preserved. This contrasts with Troodon, whose crista were ossified at least in their dorsal and ventral regions and their remaining portions either cartilaginous or too delicate to be preserved. The metotic strut of C. saharicus is reduced and medial compared to the "laterally hypertrophied" condition of non-avian maniraptors like Dromaeosaurus and Troodon, as well as primitive birds like Archaeopteryx and Hesperornis.
Name | Status | Authors | Age | Unit | Location | Notes | Images |
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Late Cretaceous |
The type species is Apsaravis ukhaana. |
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Late Cretaceous |
The type species is Limenavis patagonica. |
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Early Cretaceous |
The type species is Longipteryx chaoyangensis. |
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Early Createcous |
The type species is Yanornis martini. |
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Early Cretaceous |
The type species is Yixianornis grabaui. |
Name | Status | Authors | Age | Unit | Location | Notes | Images |
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Early Cretaceou |
The type species is Haopterus gracilis. |
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Valid |
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Early Cretaceous |
A new genus for Ornithodesmus latidens. |
Name | Status | Authors | Age | Unit | Location | Notes | Images |
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Late Permian |
Vyazniki Assemblage |
A dicynodont. Two species are described Delectosaurus arefjevi and D. berezhanensis. |
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Valid |
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Late Permian |
Vyazniki Assemblage |
A dicynodont. The type species is Interpresosaurus blomi. |
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Valid |
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Middle Triassic |
Burgersdorp Formation |
A cynodont. The type species is Lumkuia fuzzi. |
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Valid |
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Late Triassic |
Vyazniki Assemblage |
A therocephalian. The type species is Malasaurus germanus. |
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Valid |
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Late Triassic |
A cynodont. The type species is Mitredon cromptoni. |
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Valid |
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Late Triassic |
New genus for "Thrinaxodon" brasiliensis Barberena, Bonaparte & Sá Teixeira, 1987 |
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Valid |
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Late Triassic |
A cynodont. The type species is Riograndia guaibensis. |
Name | Novelty | Status | Authors | Age | Unit | Location | Notes | Images |
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gen et sp nov |
Valid |
Pigg & Rothwell |
Langhian (Middle Miocene) |
"Ho ho" site, Grande Ronde Basalt, Columbia River Basalt Group. |
Name | Novelty | Status | Authors | Age | Unit | Location | Notes | Images |
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sp nov |
Valid |
Stockey, Rothwell, & Falder |
Munce’s Hill and Gao mine sites, Paskapoo Formation |
Name | Novelty | Status | Authors | Age | Unit | Location | Notes | Images |
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sp nov |
Valid |
Pigg, Wehr, & Ickert-Bond |
As science becomes more collaborative, papers with large numbers of authors are becoming more common. To prevent the deformation of the tables, these footnotes list the contributors to papers that erect new genera and have many authors.