Timeline of stegosaur research

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Skeletal mount of Stegosaurus. Natural History Museum, London Stegosaurus.jpg
Skeletal mount of Stegosaurus .

This timeline of stegosaur research is a chronological listing of events in the history of paleontology focused on the stegosaurs, the iconic plate-backed, spike-tailed herbivorous eurypod dinosaurs that predominated during the Jurassic period. The first scientifically documented stegosaur remains were recovered from Early Cretaceous strata in England during the mid-19th century. [1] However, they would not be recognized as a distinct group of dinosaurs until Othniel Charles Marsh described the new genus and species Stegosaurus armatus in 1877, which he regarded as the founding member of the Stegosauria. [2] This new taxon originally included all armored dinosaurs. It was not until 1927 that Alfred Sherwood Romer implemented the modern use of the name Stegosauria as specifically pertaining to the plate-backed and spike-tailed dinosaurs. [1]

Contents

From the time of their earliest description, the chief mystery surrounding stegosaurs was the function of their distinctive back plates. Marsh originally interpreted them as being plates of armor that would protect against predators. In 1910, Richard Swann Lull would agree with this hypothesis. Charles Whitney Gilmore disagreed in 1914 and argued that the only protection a stegosaur could gain from its plates was to appear intimidatingly larger to potential predators. Nearly forty years later, Davitashvili argued that the plates were too fragile to be used for defense and instead used to attract mates and signal the stegosaur's rank in a social hierarchy. [3]

In the late 1970s, James O. Farlow and others would propose that the thin, blood vessel-rich plates helped absorb or lose body heat, depending on the animal's own physiological requirements. [4] This hypothesis was put forth in a broader context of scientists considering the possibility that dinosaurs may have maintained body temperatures and activity levels similar to those of modern birds and mammals, [5] in which case the plates may have served primarily to shed heat rather than gain it. In the late 1980s Buffrenil and others revived the idea that stegosaur plates were display structures, an interpretation that would continue to find favor from researchers like Main and colleagues into the 21st century. [4]

19th century

Regnosaurus jaw fragments. Regnosaurus.jpg
Regnosaurus jaw fragments.
Type specimen of Omosaurus armatus. Hul - Dacentrurus armatus.jpg
Type specimen of Omosaurus armatus .

1840s

1841

1870s

Othniel Charles Marsh's reconstruction of Stegosaurus. Stego-marsh-1896-US geological survey.png
Othniel Charles Marsh's reconstruction of Stegosaurus .

1874

1875

1876

1877

1878

1879

1880s

Holotype of Omosaurus (now Dacentrurus) armatus, from Sir Richard Owen's 1875 monograph. Dacentrurus holotype.jpg
Holotype of Omosaurus (now Dacentrurus ) armatus , from Sir Richard Owen's 1875 monograph.
Holotype of Stegosaurus stenops. Stenops.jpg
Holotype of Stegosaurus stenops .

1880

1881

1884

1887

1890s

1891

1893

20th century

1900s

Artist's restoration of Dacentrurus. Dacentrurus armatus.png
Artist's restoration of Dacentrurus .
Dacentrurus spike and limb bones. Omosaurus armatus.jpg
Dacentrurus spike and limb bones.

1901

1902

1905

1910s

1910

1911

1912

1914

Artist's restoration of Kentrosaurus. Kentrosaurus digital clay reconstruction.png
Artist's restoration of Kentrosaurus .

1915

1916

1920s

Ankylosaurs (pictured) were first distinguished from stegosaurs in 1927 by Romer. Ankylosaurus magniventris reconstruction.png
Ankylosaurs (pictured) were first distinguished from stegosaurs in 1927 by Romer.

1924

1927

Skull of Paranthodon. Paranthodon.png
Skull of Paranthodon .

1929

1940s

1944

1950s

Artist's restoration of Chialingosaurus kuani. Chialingosaurus kuani.png
Artist's restoration of Chialingosaurus kuani .

1951

1957

1960s

Fossils of Lexovisaurus. Lexovisaurus.jpg
Fossils of Lexovisaurus .

1961

1963

1966

1970s

Artist's restoration of Wuerhosaurus. Wuerhosaurus homheni.png
Artist's restoration of Wuerhosaurus .

1973

1976

Artist's restoration of Tuojiangosaurus. Tuojiangosaurus multispinus.png
Artist's restoration of Tuojiangosaurus .

1977

1978

1979

1980s

Artist's restoration of Huayangosaurus taibaii. Huayangosaurus taibaii.png
Artist's restoration of Huayangosaurus taibaii .

1980

1981

Skeletal mount of Kentrosaurus. Berlin Naturkundemuseum Dino Eingangshalle.jpg
Skeletal mount of Kentrosaurus.

1982

Skeletal mount of Chungkingosaurus jiangbeiensis. Chungkingosaurus jiangbeiensis.jpg
Skeletal mount of Chungkingosaurus jiangbeiensis .

1983

1984

Stegosaurus back plate. Stegosaurus dorsal plate - Museum of the Rockies - 2013-07-08.jpg
Stegosaurus back plate.

1985

1986

Tracks supposedly left by stegosaurs in South America may actually have been left by hadrosaurs. Maiasaur Pano-v1.jpg
Tracks supposedly left by stegosaurs in South America may actually have been left by hadrosaurs.

1987

1987

1987

1990s

Wuerhosaurus back plate Wuerhosaurus plate at the Paleozoological Museum of China.jpg
Wuerhosaurus back plate

1990

1991

1992

1993

1994

Dravidosaurus may have actually been a plesiosaur. Paleo Hall at HMNS plesiosaur.jpg
Dravidosaurus may have actually been a plesiosaur.

1996

1997

1998

Stegosaurus tail spikes. Thagomizer 01.jpg
Stegosaurus tail spikes.

1999

21st century

2000s

Main and others argued that Stegosaurus did not use its plates to regulate its body temperature. Stegosaurus ungulatus.jpg
Main and others argued that Stegosaurus did not use its plates to regulate its body temperature.

2000

Skeletal mount of Hesperosaurus mjosi. Hesperosaurus mjosi skeleton.JPG
Skeletal mount of Hesperosaurus mjosi .

2001

2004

2007

2008

2009

Artist's restoration of Miragaia longicollum. Miragaia.jpg
Artist's restoration of Miragaia longicollum .

2010s

2015

2016

2018

2019

2020s

2020

2022

See also

Footnotes

  1. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 Galton and Upchurch (2004); "Introduction", page 343.
  2. Galton and Upchurch (2004); "Table 16.1: Stegosauria", pages 344-345.
  3. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 Galton and Upchurch (2004); "Paleoecology and Behavior", page 361.
  4. 1 2 3 4 5 6 7 8 9 Galton and Upchurch (2004); "Paleoecology and Behavior", page 362.
  5. Chinsamy and Hillenius (2004); "Introduction", page 643.
  6. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 Galton and Upchurch (2004); "Table 16.1: Stegosauria", page 345.
  7. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 Galton and Upchurch (2004); "Table 16.1: Stegosauria", page 344.
  8. Benton (1990); "Racial Senility", page 379.
  9. For Woodward's speech, see Benton (1990); "Racial Senility", page 379. For a definition and discussion of racial senility, see "Post-Darwinian Interpretations", page 376.
  10. 1 2 3 4 Galton and Upchurch (2004); "Taphonomy", page 360.
  11. 1 2 3 4 Galton and Upchurch (2004); "Paleoecology and Behavior", page 360.
  12. Galton and Upchurch (2004); "Introduction", page 343. For the original publication, see Jenny and Jossen (1982)
  13. 1 2 Galton and Upchurch (2004); "Systematic and Evolution", page 358.
  14. Galton and Upchurch (2004); "Taphonomy", page 360. For the original publication, see Heinrich (1999).
  15. Chengkai et al. (2007); "Abstract", page 351.
  16. Maidment et al. (2008); "Synopsis", page 367.
  17. Mateus, Maidment and Christiansen (2009); "Abstract", page 1815.
  18. Cameron, Cameron, and Barnett (2015); in passim.
  19. Galton and Carpenter (2016); in passim.
  20. Cameron, Cameron, and Barnett (2016); in passim.
  21. T. A. Tumanova; V. R. Alifanov (2018). "First record of stegosaur (Ornithischia, Dinosauria) from the Aptian–Albian of Mongolia". Paleontological Journal. 52 (14): 1771–1779. doi:10.1134/S0031030118140186. S2CID   91559457.
  22. Marco Romano (2019). "Disparity vs. diversity in Stegosauria (Dinosauria, Ornithischia): cranial and post-cranial sub-dataset provide different signals". Historical Biology: An International Journal of Paleobiology. 31 (7): 857–865. doi:10.1080/08912963.2017.1397655. S2CID   89787668.
  23. Bao-Qiao Hao; Yong Ye; Susannah C R. Maidment; Sergio Bertazzo; Guang-Zhao Peng; Hai-Lu You (2019). "Femoral osteopathy in Gigantspinosaurus sichuanensis (Dinosauria: Stegosauria) from the Late Jurassic of Sichuan Basin, Southwestern China". Historical Biology: An International Journal of Paleobiology. 32 (8): 1–8. doi:10.1080/08912963.2018.1561673. S2CID   91554634.
  24. Maidment, Susannah C. R.; Raven, Thomas J.; Ouarhache, Driss; Barrett, Paul M. (2019-08-16). "North Africa's first stegosaur: Implications for Gondwanan thyreophoran dinosaur diversity". Gondwana Research. 77: 82–97. doi: 10.1016/j.gr.2019.07.007 . hdl: 10141/622706 . ISSN   1342-937X.
  25. Dai, H.; Li, N.; Maidment, S. C. R.; Wei, G.; Zhou, Y. X.; Hu, X. F.; Ma, Q. Y.; Wang, X. Q.; Hu, H. Q.; Peng, G. Z. (2022). "New Stegosaurs from the Middle Jurassic Lower Member of the Shaximiao Formation of Chongqing, China". Journal of Vertebrate Paleontology. 41 (5): e1995737. doi: 10.1080/02724634.2021.1995737 . S2CID   247267743.

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<i>Stegosaurus</i> Thyreophoran stegosaurid dinosaur genus from Late Jurassic period

Stegosaurus is a genus of herbivorous, four-legged, armored dinosaur from the Late Jurassic, characterized by the distinctive kite-shaped upright plates along their backs and spikes on their tails. Fossils of the genus have been found in the western United States and in Portugal, where they are found in Kimmeridgian- to Tithonian-aged strata, dating to between 155 and 145 million years ago. Of the species that have been classified in the upper Morrison Formation of the western US, only three are universally recognized: S. stenops, S. ungulatus and S. sulcatus. The remains of over 80 individual animals of this genus have been found. Stegosaurus would have lived alongside dinosaurs such as Apatosaurus, Diplodocus, Camarasaurus and Allosaurus, the latter of which may have preyed on it.

<span class="mw-page-title-main">Thyreophora</span> Extinct clade of dinosaurs

Thyreophora is a group of armored ornithischian dinosaurs that lived from the Early Jurassic until the end of the Cretaceous.

<i>Kentrosaurus</i> Extinct genus of dinosaurs from late Jurassic in Lindi Region, Tanzania

Kentrosaurus is a genus of stegosaurid dinosaur from the Late Jurassic in Lindi Region of Tanzania. The type species is K. aethiopicus, named and described by German palaeontologist Edwin Hennig in 1915. Often thought to be a "primitive" member of the Stegosauria, several recent cladistic analyses find it as more derived than many other stegosaurs, and a close relative of Stegosaurus from the North American Morrison Formation within the Stegosauridae.

<span class="mw-page-title-main">Thagomizer</span> Spiked structure on the tails of dinosaurs of the family Stegosauria

A thagomizer is the distinctive arrangement of four spikes on the tails of stegosaurian dinosaurs. These spikes are believed to have been a defensive measure against predators.

<i>Hesperosaurus</i> Extinct genus of dinosaurs

Hesperosaurus is a herbivorous stegosaurian dinosaur from the Kimmeridgian age of the Jurassic period, approximately 156 million years ago.

<i>Dacentrurus</i> Extinct species of reptile

Dacentrurus, originally known as Omosaurus, is a genus of stegosaurian dinosaur from the Late Jurassic to Early Cretaceous of Europe. Its type species, Omosaurus armatus, was named in 1875, based on a skeleton found in a clay pit in the Kimmeridge Clay in Swindon, England. In 1902 the genus was renamed Dacentrurus because the name Omosaurus had already been used for a crocodylian. After 1875, half a dozen other species would be named but perhaps only Dacentrurus armatus is valid. Finds of this animal have been limited and much of its appearance is uncertain. It was a heavily built quadrupedal herbivore, adorned with plates and spikes, reaching 8–9 metres (26–30 ft) in length and 5 metric tons in body mass.

<i>Dravidosaurus</i> Extinct species of reptile

Dravidosaurus is a controversial taxon of Late Cretaceous reptiles, variously interpreted as either a ornithischian, possibly stegosaurian, dinosaur or a plesiosaur. The genus contains a single species, D. blanfordi, known from mostly poorly preserved fossils from the Coniacian of southern India.

<i>Chialingosaurus</i> Extinct genus of dinosaurs

Chialingosaurus is a genus of herbivorous stegosaurian dinosaur similar to Kentrosaurus from the Upper Shaximiao Formation, Late Jurassic beds in Sichuan Province in China. Its age makes it one of the oldest species of stegosaurs, living about 160 million years ago. Since it was an herbivore, scientists think that Chialingosaurus probably ate ferns and cycads, which were plentiful during the period when Chialingosaurus was alive.

<i>Wuerhosaurus</i> Extinct genus of dinosaurs

Wuerhosaurus is a genus of stegosaurid dinosaur from the Early Cretaceous Period of China and Mongolia. As such, it was one of the last genera of stegosaurians known to have existed.

<i>Lexovisaurus</i> Extinct genus of reptiles

Lexovisaurus is a genus of stegosaur from mid-to-Late Jurassic Europe, 165.7-164.7 mya. Fossils of limb bones and armor fragments have been found in middle to late Jurassic-aged strata of England and France.

<i>Tuojiangosaurus</i> Extinct genus of dinosaurs

Tuojiangosaurus is a genus of herbivorous stegosaurian dinosaur from the Late Jurassic Period, recovered from the Upper Shaximiao Formation of what is now Sichuan Province in China.

<i>Paranthodon</i> Stegosaurian dinosaur genus from Early Cretaceous South Africa

Paranthodon is a genus of stegosaurian dinosaur that lived in what is now South Africa during the Early Cretaceous, between 139 and 131 million years ago. Discovered in 1845, it was one of the first stegosaurians found. Its only remains, a partial skull, isolated teeth, and fragments of vertebrae, were found in the Kirkwood Formation. British paleontologist Richard Owen initially identified the fragments as those of the pareiasaur Anthodon. After remaining untouched for years in the British Museum of Natural History, the partial skull was identified by South African paleontologist Robert Broom as belonging to a different genus; he named the specimen Palaeoscincus africanus. Several years later, Hungarian paleontologist Franz Nopcsa, unaware of Broom's new name, similarly concluded that it represented a new taxon, and named it Paranthodon owenii. Since Nopcsa's species name was assigned after Broom's, and Broom did not assign a new genus, both names are now synonyms of the current binomial, Paranthodon africanus. The genus name combines the Ancient Greek para (near) with the genus name Anthodon, to represent the initial referral of the remains.

<span class="mw-page-title-main">Stegosauria</span> Extinct clade of dinosaurs

Stegosauria is a group of herbivorous ornithischian dinosaurs that lived during the Jurassic and early Cretaceous periods. Stegosaurian fossils have been found mostly in the Northern Hemisphere, predominantly in what is now North America, Europe, Africa, South America and Asia. Their geographical origins are unclear; the earliest unequivocal stegosaurian, Huayangosaurus taibaii, lived in China.

<span class="mw-page-title-main">Stegosauridae</span> Extinct family of dinosaurs

Stegosauridae is a family of thyreophoran dinosaurs within the suborder Stegosauria. The clade is defined as all species of dinosaurs more closely related to Stegosaurus than Huayangosaurus. The name ‘Stegosauridae’ is thus a stem-based name taken from the well-represented genus – Stegosaurus. Fossil evidence of stegosaurids, dating from the Middle Jurassic through the Early Cretaceous, have been recovered from North America, Eurasia and Africa.

<i>Chungkingosaurus</i> Extinct genus of dinosaurs

Chungkingosaurus, meaning "Chongqing Lizard", is a genus of herbivorous dinosaur from the Late Jurassic Upper Shaximiao Formation in what is now China. It is a member of the Stegosauria.

<i>Hypsirhophus</i> Genus of dinosaurs

Hypsirhophus is a genus of stegosaurian dinosaurs. It contains a single species, Hypsirhophus discurus, which is known only from a fragmentary specimen. The fossil consists of partial vertebrae from the back, three from the tail, and a piece of rib.

<i>Loricatosaurus</i> Extinct genus of dinosaurs

Loricatosaurus is a Stegosaurid genus from Callovian-age rocks of England and France.

<i>Alcovasaurus</i> Extinct genus of dinosaurs

Alcovasaurus, alternatively known as Miragaia longispinus, is a genus of herbivorous stegosaurian dinosaur that lived in the Late Jurassic. It was found in the Morrison Formation of Natrona County, Wyoming, United States. The type species is Stegosaurus longispinus, later given the genus Alcovasaurus, and in 2019 recombined as Miragaia longispinus.

<span class="mw-page-title-main">Timeline of ankylosaur research</span>

This timeline of ankylosaur research is a chronological listing of events in the history of paleontology focused on the ankylosaurs, quadrupedal herbivorous dinosaurs who were protected by a covering bony plates and spikes and sometimes by a clubbed tail. Although formally trained scientists did not begin documenting ankylosaur fossils until the early 19th century, Native Americans had a long history of contact with these remains, which were generally interpreted through a mythological lens. The Delaware people have stories about smoking the bones of ancient monsters in a magic ritual to have wishes granted and ankylosaur fossils are among the local fossils that may have been used like this. The Native Americans of the modern southwestern United States tell stories about an armored monster named Yeitso that may have been influenced by local ankylosaur fossils. Likewise, ankylosaur remains are among the dinosaur bones found along the Red Deer River of Alberta, Canada where the Piegan people believe that the Grandfather of the Buffalo once lived.

References