Richardoestesia

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Richardoestesia
Temporal range: Late Cretaceous, 90–66  Ma
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Possible Early Cretaceous (Barremian) records from teeth of the Cedar Mountain Formation, but see [1] .
Richardoestesia.png
Tooth of cf. R. gilmorei with close up of denticles
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Dinosauria
Clade: Saurischia
Clade: Theropoda
Clade: Coelurosauria
Genus: Richardoestesia
Currie, Rigby & Sloan, 1990
Type species
Richardoestesia gilmorei
Currie, Rigby & Sloan, 1990
Other species
  • R. isosceles
    Sankey, 2001
  • R. asiatica ? Averianov & Sues, 2013
Synonyms
  • Asiamericana asiatica? Nesov, 1995
  • Ricardoestesia gilmoreiCurrie, Rigby & Sloan, 1990

Richardoestesia is a morphogenus of theropod dinosaur teeth, originally described from the Late Cretaceous of what is now Canada, the United States and Kazakhstan. It currently contains two species, R. gilmorei and R. isosceles, and a possible third, R. asiatica . It has been used as a morphotaxon to describe other theropod teeth widely displaced in time and space from the type species. If all teeth assigned to the genus are truly reflective of the animals biology and taxonomic state (as some teeth go as far back as the Late Jurassic), it would have been one of the longest lasting dinosaur genera, perhaps also being the most widely distributed.

Contents

History

Tooth of cf. R. isosceles with close up of denticles Richardoestesia isosceles.png
Tooth of cf. R. isosceles with close up of denticles

The jaws were found in 1917 by Charles Hazelius Sternberg and sons in the Dinosaur Provincial Park in Alberta at the Little Sandhill Creek site. In 1924 Charles Whitney Gilmore named Chirostenotes pergracilis and referred the jaws to this species. [2] In the 1980s it became clear that Chirostenotes was an oviraptorosaur to which the long jaws could not have belonged. Therefore, in 1990 Phillip Currie, John Keith Rigby and Robert Evan Sloan named a separate species: Richardoestesia gilmorei. [3]

The genus is named for Richard Estes, to honor his important work [4] on small vertebrates and especially theropod teeth of the Late Cretaceous. The naming authors actually intended to use the spelling Ricardoestesia, Ricardus being the normal latinisation of "Richard". However, except in one overlooked figure caption, the editors of the paper altered the spelling to include the 'h'. [5] Ironically, in 1991 George Olshevsky in a species list also used the spelling Richardoestesia, and indicated Ricardoestesia to be the misspelling, unaware that the original authors actually intended the name to be spelled this way. As a result, under ICZN rules, he acted as "first revisor" choosing between the two spelling variants of the original publication and inadvertently made the misspelt name official. Subsequently, the original authors have adopted the spelling Richardoestesia. The specific name honors Gilmore.

Species

The holotype specimen of Richardoestesia gilmorei (NMC 343) consists of a pair of lower jaws found in the upper Judith River Group, dating from the Campanian age, about 75 million years ago. The jaws are slender and rather long, 193 millimeters, but the teeth are small and very finely serrated with five to six denticles per millimeter. The serration density is a distinctive trait of the species.

In 2001, Julia Sankey named a second species: Richardoestesia isosceles, based on a tooth, LSUMGS 489:6238, from the Texan Aguja Formation, which is of a longer and less recurved type. [6] The teeth of R. isosceles have also been identified as crocodyliform in shape, possibly belonging to a sebecosuchian. [7]

In 2013 a study assumed that the teeth of the coelurosaur Asiamericana asiatica , from the CBI-14 site of the Bissekty Formation in Kazakhstan, [8] [ page needed ] were identical to those of Richardoestesia isosceles, and renamed the species into Richardoestesia asiatica. [9] A subsequent study confirmed this in 2019. [10] The holotype of R. asiatica is CCMGE 460/12457, [8] [ page needed ] and two other teeth (ZIN PH 1110/ 16 and ZIN PH 1129/16) are also known. [10]

Referred teeth. Small theropod tooth morphotypes (cropped).png
Referred teeth.

Classification

Referred teeth from the San Juan Basin Richardoestesia teeth.png
Referred teeth from the San Juan Basin

Richardoestesia-like teeth have been found in many Late Cretaceous geological formations, including the Horseshoe Canyon Formation, the Scollard Formation, Hell Creek Formation, Ferris Formation, and the Lance Formation (dated to about 66 million years ago). Similar teeth have been referred to this genus from as early as the Barremian age (Cedar Mountain Formation, 125 million years ago). [1]

Because of the disparity in location and time of the many referred teeth, researchers have cast doubt on the idea that they all belong to the same genus or species, and the genus is best considered a form taxon. A comparative study of the teeth published in 2013 demonstrated that both R. gilmorei and R. isosceles were only definitively present in the Dinosaur Park Formation, dated to between 76.5 and 75 million years ago. R. isosceles was also present in the Aguja Formation, roughly the same age. All other referred teeth most likely belong to different species, which have not been named due to the lack of body fossils for comparison. [11]

Hypothetical life restoration as a dromaeosaur Ojo Alamo cf. Richardoestesia sp profile reconstruction.jpg
Hypothetical life restoration as a dromaeosaur

Fossils of Richardoestesia have also been found in the Tremp Formation of northeastern Spain (Blasi 2 member). [12] The oldest fossils that have been referred to Richardoestesia come from the Jurassic of Portugal. [13]

Paleobiology

At least a few studies have speculated a piscivorous lifestyle for Richardoestesia, due to its vast distribution as well as predominance in marine sites. [14] [15]

Related Research Articles

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

Troodon is a former wastebasket taxon and a potentially dubious genus of relatively small, bird-like theropod dinosaurs definitively known from the Campanian age of the Late Cretaceous period. It includes at least one species, Troodon formosus, known from Montana. Discovered in October 1855, T. formosus was among the first dinosaurs found in North America, although it was thought to be a lizard until 1877. Several well-known troodontid specimens from the Dinosaur Park Formation in Alberta were once believed to be members of this genus. However, recent analyses in 2017 have found this genus to be undiagnostic and referred some of these specimens to the genus Stenonychosaurus some to the genus Latenivenatrix, and some to the genus Pectinodon. The genus name is Ancient Greek for "wounding tooth", referring to the teeth, which were different from those of most other theropods known at the time of their discovery. The teeth bear prominent, apically oriented serrations. These "wounding" serrations, however, are morphometrically more similar to those of herbivorous reptiles, and suggest a possibly omnivorous diet.

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

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

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<span class="mw-page-title-main">Dinosaur Provincial Park</span> Provincial park in Alberta, Canada

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

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

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

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<i>Caenagnathus</i> Genus of dinosaur from the Late Cretaceous period

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

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Asiamericana is a dubious genus of coelurosaur known only from isolated teeth found in the Bissekty Formation of Uzbekhistan. It was named to recognize the occurrence of similar fossil teeth in Central Asia and North America. These regions once formed a connected land mass, during the Cretaceous period.

<span class="mw-page-title-main">Dinosaur Park Formation</span> Uppermost member of the Belly River Group geologic unit in Alberta, Canada

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<span class="mw-page-title-main">Horseshoe Canyon Formation</span> Geological formation in Canada

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

Caenagnathidae is a family of derived caenagnathoid dinosaurs from the Cretaceous of North America and Asia. They are a member of the Oviraptorosauria, and relatives of the Oviraptoridae. Like other oviraptorosaurs, caenagnathids had specialized beaks, long necks, and short tails, and would have been covered in feathers. The relationships of caenagnathids were long a puzzle. The family was originally named by Raymond Martin Sternberg in 1940 as a family of flightless birds. The discovery of skeletons of the related oviraptorids revealed that they were in fact non-avian theropods, and the discovery of more complete caenagnathid remains revealed that Chirostenotes pergracilis, originally named on the basis of a pair of hands, and Citipes elegans, originally thought to be an ornithomimid, named from a foot, were caenagnathids as well.

<span class="mw-page-title-main">Aguja Formation</span> Geological formation in North America

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

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<i>Leptorhynchos gaddisi</i> Extinct species of dinosaur

Leptorhynchos is an extinct genus of caenagnathid theropod from the Late Cretaceous of what is now the US state of Texas, although it has been suggested to also exist in Alberta and South Dakota. The type species is L. gaddisi, and it is currently the only widely accepted valid species. The generic name of Leptorhynchos comes from the Greek "leptos" meaning "small" and "rhynchos" meaning "beak". The specific epithet is in honor of the Gaddis family, who owned the land on which the holotype was discovered.

References

  1. 1 2 Kirkland JI, Lucas SG, Estep JW (1998). "Cretaceous dinosaurs of the Colorado Plateau". In Kirkland JI, Lucas SG, Estep JW (eds.). Lower and Middle Cretaceous Terrestrial Ecosystems. New Mexico Museum of Natural History and Science Bulletin. Vol. 14. pp. 79–89.
  2. Gilmore CW (1924). "A new coelurid dinosaur from the Belly River Cretaceous of Alberta". Canada Department of Mines Geological Survey Bulletin (Geological Series). 38 (43): 1–12.
  3. Currie PJ, Rigby KJ, Sloan RE (1990). "Theropod teeth from the Judith River Formation of southern Alberta, Canada". In Currie PJ, Carpenter K (eds.). Dinosaur Systematics: Perspectives and Approaches. Cambridge: Cambridge University Press. pp. 107–125.
  4. Estes R (1964). Fossil vertebrates from the Late Cretaceous Lance Formation, eastern Wyoming. University of California Publications in Geological Sciences. Vol. 49.
  5. "Re: "Mega-raptors" and the high frequency of undescribed dromaeosaurs in lists" (Mailing list). 22 November 1997. Archived from the original on 6 August 2016.
  6. Sankey JT (2001). "Late Campanian southern dinosaurs, Aguja Formation, Big Bend, Texas" (PDF). Journal of Paleontology. 75 (1): 208–215. doi:10.1666/0022-3360(2001)075<0208:LCSDAF>2.0.CO;2.
  7. Company J, Suberbiola XP, Ruiz-Omeñaca JI, Buscalioni AD (2005). "A new species of Doratodon (Crocodyliformes: Ziphosuchia) from the Late Cretaceous of Spain". Journal of Vertebrate Paleontology. 25 (2): 343–353. doi:10.1671/0272-4634(2005)025[0343:ANSODC]2.0.CO;2.
  8. 1 2 Nessov LA (1995). Динозавры северной Евразии: Новые данные о составе комплексов, экологии и палеобиогеографии [Dinosaurs of Northern Eurasia: new data about assemblages, ecology and paleobiogeography](PDF) (in Russian). St. Petersburg, Russia: Scientific Research Institute of the Earth's Crust, St. Petersburg State University. in Russian with short English, German, and French abstracts
  9. Sues HD, Averianov A (2013). "Enigmatic teeth of small theropod dinosaurs from the Upper Cretaceous (Cenomanian–Turonian) of Uzbekistan". Canadian Journal of Earth Sciences. 50 (3): 306–314. Bibcode:2013CaJES..50..306S. doi:10.1139/e2012-033.
  10. 1 2 Averianov A, Sues HD (2019). "Morphometric analysis of the teeth and taxonomy of the enigmatic theropod Richardoestesia from the Upper Cretaceous of Uzbekistan". Journal of Vertebrate Paleontology. 39 (3): e1614941. Bibcode:2019JVPal..39E4941A. doi:10.1080/02724634.2019.1614941.
  11. Larson DW, Currie PJ (2013). "Multivariate Analyses of Small Theropod Dinosaur Teeth and Implications for Paleoecological Turnover through Time". PLOS ONE. 8 (1): e54329. Bibcode:2013PLoSO...854329L. doi: 10.1371/journal.pone.0054329 . PMC   3553132 . PMID   23372708.
  12. "Blasi 2". Fossilworks .
  13. Zinke J (1 April 1998). "Small theropod teeth from the Upper Jurassic coal mine of Guimarota (Portugal)". Paläontologische Zeitschrift. 72 (1): 179–189. Bibcode:1998PalZ...72..179Z. doi:10.1007/BF02987825.
  14. Carbot-Chanona G, Rivera-Sylva HE (December 2011). "Presence of a maniraptoriform dinosaur in the Late Cretaceous (Maastrichtian) of Chiapas, Southern Mexico". Boletín de la Sociedad Geológica Mexicana. 63 (3): 393–398. doi:10.18268/BSGM2011v63n3a2.
  15. Longrich N (2008). "Small theropod teeth from the Lance Formation of Wyoming, USA". In Sankey JT, Baszio S (eds.). Vertebrate microfossil assemblages: their role in paleoecology and paleobiogeography. Bloomington: Indiana University Press. pp. 135–158.

Further reading