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Elasmotherium

Elasmotherium is an extinct genus of large rhinoceros endemic to Eurasia during Late Miocene through to the Late Pleistocene, with the youngest reliable dates around 39,000 years ago. It was the last surviving member of Elasmotheriinae, a distinctive group of rhinoceroses separate from the group that contains living rhinoceros (Rhinocerotinae).[2]

Elasmotherium
Temporal range: Late Miocene to Late Pleistocene, 7–0.039 Ma
Reconstructed E. caucasicum skeleton, Azov Museum of History, Archaeology and Palaeontology
Scientific classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Perissodactyla
Family: Rhinocerotidae
Subfamily: Elasmotheriinae
Genus: Elasmotherium
J. Fischer, 1808[1]
Type species
Elasmotherium sibiricum
Other Species
  • E. caucasicum
  • E. chaprovicum
  • E. peii
  • E. primigenium
Approximate range map for Elasmotherium
Synonyms
  • Stereoceros
  • Enigmatherium
  • E. fischeri = E. sibiricum
  • E. inexpectatum = E. caucasicum

Five species are recognised. The genus first appeared in the Late Miocene in present-day China, likely having evolved from Sinotherium, before spreading to the Pontic–Caspian steppe, the Caucasus and Central Asia.[3] The best known Elasmotherium species, E. sibiricum, sometimes called the Siberian unicorn,[4] was the size of a mammoth and is often conjectured to have borne a single very large horn. However, no horn has ever been found, and other authors have conjectured that the horn was likely much smaller. Like all rhinoceroses, elasmotheres were herbivorous. Unlike any other rhinos and any other ungulates aside from some notoungulates, its high-crowned molars were ever-growing, and it was likely adapted for a grazing diet. Its legs were longer than those of other rhinos and were adapted for galloping, giving it a horse-like gait.

Taxonomy edit

 
The "Moscow mandible", holotype of E. sibiricum

Elasmotherium was first described in 1809 by German/Russian palaeontologist Gotthelf Fischer von Waldheim based on a left lower jaw, four molars, and the tooth root of the third premolar, which was gifted to Moscow University by princess Ekaterina Dashkova in 1807. He first announced it at an 1808 presentation before the Moscow Society of Naturalists.[5] The genus name derives from Ancient Greek elasmos "laminated" and therion "beast" in reference to the laminated folding of the tooth enamel; and the species name sibericus is probably a reference to the predominantly Siberian origin of princess Dashkova's collection. However, the specimen's exact origins are unknown. In 1877, German naturalist Johann Friedrich von Brandt placed it into the newly erected subfamily Elasmotheriinae, separate from modern rhinos.[6] In 1997, the McKenna/Bell classification considered Elasmotherium to be closely related to the wooly and modern rhinos, and placed it into the subfamily Rhinocerotinae. A complete mitochondrial genome obtained from a specimen of E. sibiricum vindicated von Brandt, finding it to be the sister taxon to all living rhinoceroses, with an estimated divergence time of 47.4 million years ago, with a 95% highest posterior density of 41.9–53.2 Ma.[2]

The genus is known from hundreds of find sites, mainly of cranial fragments and teeth, but in some cases nearly complete skeletons of post-cranial bones, scattered over Eurasia from Eastern Europe to China.[7] Dozens of crania have been reconstructed and given archaeological identifiers. The division into species is based mainly on the fine distinctions of the teeth and jaws and the shape of the skull.[8]

Evolution edit

Rhinoceroses are divided into two subfamilies, Rhinocerotinae and Elasmotheriinae, which diverged perhaps 47.3 mya, 35 mya at the latest.[2] Elasmotherium is the only known member of the latter from after the Miocene, others becoming extinct with the expansion of savannas.[9] The oldest known species of Elasmotherium is Elasmotherium primigenium from the Late Miocene of Dingbian County in Shaanxi, China. Elasmotherium likely evolved from Sinotherium, a genus of elasmothere also found in China.[10] Elasmotherium arrived in Eastern Europe around 2.5 million years ago, during the earliest part of the Pleistocene epoch.[11]

Hypsodonty, a dentition pattern where the molars have high crowns and the enamel extends below the gum line, is thought to be a characteristic of Elasmotheriinae,[12] perhaps as an adaptation to the heavier grains featured in riparian zones on riversides.[13]

Species edit

There are four chronospecies of Elasmotherium aside from the aforementioned E. primigenium, which are - from oldest to youngest - E. chaprovicum, E. peii, E. caucasicum and E. sibiricum, and which together span from the Late Pliocene to the Late Pleistocene.[3]

 
Skeletal reconstruction of Elasmotherium sibiricum
 
First published restoration (1878) of E. sibiricum, by Rashevsky, under supervision of A.F. Brant

An elasmotherian species turned up in the preceding Khaprovian or Khaprov Faunal Complex, which was at first taken to be E. caucasicum,[14] and then on the basis of the dentition was redefined as a new species, E. chaprovicum (Shvyreva, 2004), named after the Khaprov Faunal Complex.[8] The Khaprov is in the Middle Villafranchian, MN17, which spans the Piacenzian of the Late Pliocene and the Gelasian of the Early Pleistocene of Northern Caucasus, Moldova and Asia and has been dated to 2.6–2.2 Ma.[15]

E. peii was first described by (Chow, 1958) for remains found in Shaanxi, China.[16] Additional remains from Shaanxi were described in 2018[17] The species is also known from numerous remains from the classical range of Elasmotherium, some sources have considered this species to be a synonym of E. caucasicum, but it is currently considered distinct.[3] it is found during the Psekups faunal complex between 2.2 and 1.6 Ma.[3]

E. caucasicum was first described by Russian palaeontologist Aleksei Borissiak in 1914, who said it apparently flourished in the Black Sea region as a member of the Early Pleistocene Tamanian Faunal Unit (1.1–0.8 Ma, Taman Peninsula). It is the most commonly found mammal of the assemblage. E. caucasicum is thought to be more primitive than E. sibiricum and perhaps represents an ancestral stock.[18][19] It is also known in northern China from the Early Pleistocene Nihewan Faunal assemblage and were extinct at approximately 1.6 Ma. This suggests Elasmotherium developed separately in Russia and China.[13]

 
Paleolithic art from Rouffignac Cave, France interpreted as Elasmotherium[6]

E. sibiricum, described by Johann Fischer von Waldheim in 1808 and chronologically the latest species of the sequence appeared in the Middle Pleistocene, ranging from southwestern Russia to western Siberia and southward into Ukraine and Moldova.[20]

Description edit

Elasmotherium is typically reconstructed as a woolly animal, generally based on the woolliness exemplified in contemporary megafauna such as mammoths and the woolly rhino. However, it is sometimes depicted as bare-skinned like modern rhinos. In 1948, Russian palaeontologist Valentin Teryaev suggested it was semi-aquatic with a dome-like horn, and resembled a hippo because the animal had 4 toes like a wetland tapir rather than the 3 toes in other rhinos, but Elasmotherium has since been shown to have had only 3 functional toes,[6] and Teryaev's reconstruction has not garnered much scientific attention.[6][13]

The known specimens of E. sibiricum reach up to 4.5 m (15 ft) in length, with shoulder heights up to 2.5 m (8 ft 2 in), while E. caucasicum reaches at least 5 m (16 ft) in body length with an estimated mass of 3.5–5 tonnes (3.9–5.5 short tons),[6][21] making Elasmotherium the largest rhinos of the Quaternary.[2] Both species were among the largest rhinos, comparable in size to the woolly mammoth and larger than the contemporary woolly rhinoceros.[22][9] The feet were unguligrade, the front larger than the rear, with 3 digits at the front and rear, with a vestigial fifth metacarpal.[23]

Dentition edit

 
Size of Elasmotherium (light grey) compared to a human and other rhinos
 
E. caucasicum reconstructed without hair
 
E. sibiricum skull cast at the Museum für Naturkunde, Berlin

Like other rhinos, Elasmotherium had two premolars and three molars for chewing, and lacked incisors and canines, relying instead on a prehensile lip to strip food.[6] Elasmotherium were euhypsodonts, with large tooth crowns and enamel extending below the gum line, and continuously growing teeth.

Elasmotherium fossils rarely show evidence of tooth roots.[citation needed]

Horn edit

Elasmotherium is traditionally thought to have had a keratinous horn, indicated by a circular dome on the forehead, with a 13-centimetre (5-inch) deep, furrowed surface, and a circumference of 90 cm (3 feet). The furrows are interpreted as the seats of blood vessels for horn-generating tissue.[24][25]

 
Restoration of E. sibiricum

In rhinos, the horn is not attached to bone, but grows from the surface of a dense skin tissue, anchoring itself by creating bone irregularities and rugosities.[26] The outermost layer cornifies.[27] As the layers age, the horn loses diameter by degradation of the keratin due to ultraviolet light, drying out, and continual wearing.[28] However, melanin and calcium deposits in the centre harden the keratin there, which gives the horn its distinctive shape.[29]

There was likely a large hump of muscle on the back, which is generally thought to have supported a heavy horn.[30]

A 2021 study challenges assumptions of Elasmotherium having had a horn by comparing its cranial dome and neck musculature to those of modern rhinos. The study finds that both are ill-suited for a large horn and more likely are indicative of a smaller horn, and that the dome could function as a resonating chamber of some sort, akin to that of Rusingoryx and hadrosaur crests.[31]

Palaeobiology edit

Diet edit

 
Restoration of E. sibiricum in a steppe environment

Modern hypsodont hoofed mammals are generally grazers of open environments,[32] with hypsodonty possibly an adaptation to chewing tough, fibrous grass.[33] Elasmotherium dental wearing is similar to that of the grazing white rhino,[34] and both of their heads have a downward orientation, indicating a similar lifestyle and an ability to only reach low-lying plants. In fact, the head of Elasmotherium had the most obtuse angle of any rhinoceros, and could only reach the lowest levels and therefore must have grazed habitually.[25] Elasmotherium also displays euhypsodonty, which is typically seen in rodents,[35] and dental physiology could have been influenced by pulling up food from moist, grainy soil. Therefore, they may have inhabited both mammoth steppeland and riparian riversides, similar to contemporary mammoths.[13]

Movement edit

Elasmotherium had similar running limbs to the white rhinoceros–which run at 30 km/h (19 mph) with a top speed of 40–45 km/h (25–28 mph). However, Elasmotherium had double the weight–about 5 t (5.5 short tons)–and consequently had a more restricted gait and mobility, likely achieving much slower speeds. Elephants, weighing 2.5–11 t (2.8–12.1 short tons), cannot exceed a speed of 20 km/h (12 mph).[36]

Extinction edit

Elasmotherium was previously thought to have gone extinct around 200,000 years ago as part of normal extinction,[2] but E. sibiricum skull fragments from the Pavlodar Region, Kazakhstan, shows its persistence in the Western Siberian Plain about 36,000–35,000 years ago.[2] Isolated remains dating to 50,000 years ago are known from the Siberian Smelovskaya and Batpak Caves, likely dragged there by a predator.[37]

This timing is roughly coincident with the Pleistocene extinction, during which many mammal species with body weights >45 kg died out. This coincided with a shift to a cooler climate–which resulted in replacement of grasses and herbs by lichens and mosses–and the migration of modern humans into the area.[2]

See also edit

Notes edit

  1. ^ "Elasmotherium". PaleoBiology Database: Basic info. National Center for Ecological Analysis and Synthesis. 2000. Retrieved 23 March 2011.
  2. ^ a b c d e f g Kosintsev, P.; Mitchell, K. J.; Devièse, T.; van der Plicht, J.; Kuitems, M.; Petrova, E.; Tikhonov, A.; Higham, T.; Comeskey, D.; Turney, C.; Cooper, A.; van Kolfschoten, T.; Stuart, A. J.; Lister, A. M. (2019). "Evolution and extinction of the giant rhinoceros Elasmotherium sibiricum sheds light on late Quaternary megafaunal extinctions". Nature Ecology & Evolution. 3 (1): 31–38. doi:10.1038/s41559-018-0722-0. hdl:11370/78889dd1-9d08-40f1-99a4-0e93c72fccf3. PMID 30478308. S2CID 53726338.
  3. ^ a b c d Schvyreva, A.K. (August 2015). "On the importance of the representatives of the genus Elasmotherium (Rhinocerotidae, Mammalia) in the biochronology of the Pleistocene of Eastern Europe". Quaternary International. 379: 128–134. Bibcode:2015QuInt.379..128S. doi:10.1016/j.quaint.2015.03.052.
  4. ^ Kosintsev, Pavel; et al. (2019). "Evolution and extinction of the giant rhinoceros Elasmotherium sibiricum sheds light on late Quaternary megafaunal extinctions". Nature Ecology and Evolution. 3 (1): 31–38. doi:10.1038/s41559-018-0722-0. hdl:11370/78889dd1-9d08-40f1-99a4-0e93c72fccf3. PMID 30478308. S2CID 53726338.
  5. ^ Fischer, G. (1809). "Sur L'Elasmotherium et le Trogontothérium". Mémoires de la Société des naturalistes de Moscou. Moscow: Imprimerie de l'Université Impériale. 2: 250–268..
  6. ^ a b c d e f Zhegallo, V.; Kalandadze, N.; Shapovalov, A.; Bessudnova, Z.; Noskova, N.; Tesakova, E. (2005). "On the fossil rhinoceros Elasmotherium (including the collections of the Russian Academy of Sciences)" (PDF). Cranium. 22 (1): 17–40.
  7. ^ Tleuberdina, Piruza; Nazymbetova, Gulzhan (2010). "Distribution of Elasmotherium in Kazakhstan". In Titov, V.V.; Tesakov, A.S. (eds.). (PDF). Rostov-on-Don: Russian Academy of Science. pp. 171–173. Archived from the original (PDF) on 28 September 2010. Retrieved 26 March 2011.
  8. ^ a b Titov, V.V. (2008). Late Pliocene large mammals from Northeastern Sea of Azov Region (PDF) (in Russian and English). Rostov-on-Don: SSC RAS Publishing.
  9. ^ a b Cerdeño, Esperenza (1998). "Diversity and evolutionary trends of the Family Rhinocerotidae (Perissodactyla)" (PDF). Palaeo. 141 (1–2): 13–34. Bibcode:1998PPP...141...13C. doi:10.1016/S0031-0182(98)00003-0.
  10. ^ Sun, Danhui; Deng, Tao; Jiangzuo, Qigao (26 April 2021). "The most primitive Elasmotherium (Perissodactyla, Rhinocerotidae) from the Late Miocene of northern China". Historical Biology. 34 (2): 201–211. doi:10.1080/08912963.2021.1907368. ISSN 0891-2963. S2CID 235558419.
  11. ^ Schvyreva, A.K. (27 August 2015). "On the importance of the representatives of the genus Elasmotherium (Rhinocerotidae, Mammalia) in the biochronology of the Pleistocene of Eastern Europe". Quaternary International. 379: 128–134. Bibcode:2015QuInt.379..128S. doi:10.1016/j.quaint.2015.03.052.
  12. ^ Antoine 2003, p. 109
  13. ^ a b c d Noskova, N.G. (2001). "Elasmotherians – evolution, distribution and ecology". In Cavarretta, G.; Gioia, P.; Mussi, M.; et al. (eds.). The World of Elephants (PDF). Roma: Consiglio Nazionale delle Ricerche. pp. 126–128. ISBN 978-88-8080-025-5.
  14. ^ Logvynenko, Vitaliy. "The Development of the Late Pleistocene to Early Middle Pleistocene Large Mammal Fauna of Ukraine" (PDF). 18th International Senckenberg Conference 2004 in Weimar (Abstracts). Senckenberg Gesellschaft für Naturforschung (SGN).
  15. ^ Bajgusheva, Vera S.; Titov, Vadim V. "Results of the Khapry Faunal Unit revision" (PDF). 18th International Senckenberg Conference 2004 in Weimar (Abstracts). Senckenberg Gesellschaft für Naturforschung (SGN).
  16. ^ Chow, M.C., 1958. New elasmotherine Rhinoceroses from Shansi. Vertebrato PalA-siatica 2, 135-142.
  17. ^ Tong, Hao‑wen; Chen, Xi; Zhang, Bei (1 September 2018). "New postcranial bones of elasmotherium peii from shanshenmiaozui in Nihewan basin, Northern China". Quaternaire (vol. 29/3): 195–204. doi:10.4000/quaternaire.10010. ISSN 1142-2904. S2CID 135026963.
  18. ^ Deng & Zheng 2005, p. 119
  19. ^ Deng & Zheng 2005, p. 112
  20. ^ Baigusheva, Vera; Titov, Vadim (2010). "Pleistocene Large Mammal Associations of the Sea of Azov and Adjacent Regions". In Titov, V.V.; Tesakov, A.S. (eds.). (PDF). Rostov-on-Don: Russian Academy of Science. pp. 24–27. Archived from the original (PDF) on 28 September 2010. Retrieved 26 March 2011.
  21. ^ Schvyreva, A.K. (2016). Эласмотерии плейстоцена Евразии (PDF) (in Russian). pp. 103–105.
  22. ^ Cerdeño, Esperanza; Nieto, Manuel (1995). "Changes in Western European Rhinocerotidae related to climatic variations" (PDF). Palaeo. 114 (2–4): 328. Bibcode:1995PPP...114..325C. doi:10.1016/0031-0182(94)00085-M.
  23. ^ Belyaeva, E.I. (1977). "About the Hyroideum, Sternum and Metacarpale V Bones of Elasmotherium sibiricum Fischer (Rhinocerotidae)" (PDF). Journal of the Palaeontological Society of India. 20: 10–15.
  24. ^ Brandt, Alexander; Lockyer, Norman (8 August 1878). "The Elasmotherium". Nature. XVIII (458): 287–389. Bibcode:1878Natur..18R.387.. doi:10.1038/018387b0.
  25. ^ a b van der Made, Jan; Grube, René (2010). "The rhinoceroses from Neumark-Nord and their nutrition". In Meller, Harald (ed.). Elefantenreich – Eine Fossilwelt in Europa (PDF). Halle/Saale. pp. 382–394.
  26. ^ Hieronymus 2009, pp. 221–223
  27. ^ Hieronymus 2009, p. 24
  28. ^ Hieronymus 2009, p. 27
  29. ^ Hieronymus 2009, p. 28
  30. ^ Hieronymus 2009, p. 36
  31. ^ Titov, Vadim V.; Baigusheva, Vera S.; Uchytel', Roman S. (16 November 2021). "The experience in reconstructing of the head of Elasmotherium (Rhinocerotidae)" (PDF). Russian Journal of Theriology. 20 (2): 173–182. doi:10.15298/rusjtheriol.20.2.06. ISSN 1682-3559. S2CID 244138119.
  32. ^ Mendoza, M.; Palmqvist, P. (February 2008). "Hypsodonty in ungulates: an adaptation for grass consumption or for foraging in open habitat?". Journal of Zoology. 273 (2): 134–142. doi:10.1111/j.1469-7998.2007.00365.x.
  33. ^ MacFadden, Bruce J. (2000). "Origin and evolution of the grazing guild in Cenozoic New World terrestrial mammals". In Sues, Hans-Dieter (ed.). Evolution of Herbivory in Terrestrial Vertebrates: Perspectives from the Fossil Record. Cambridge: Cambridge University Press. pp. 226. ISBN 9780511549717.
  34. ^ Wood, Horace Elmer, 2nd (1938). "Causal Factors Shortening Tooth Series with Age". Journal of Dental Research. 17 (1): 1–13. doi:10.1177/00220345380170010101. S2CID 209330196.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link)
  35. ^ von Koenigswald, Wighart; Goin, Francisco; Pascual, Rosendo (1999). "Hypsodonty and enamel microstructure in the Paleocene gondwanatherian mammal Sudamerica amerghinoi" (PDF). Acta Palaeontologica Polonica. 44 (3): 263–300.
  36. ^ Paul, Gregory S. (December 1998). (PDF). Gaia (15): 258–259. Archived from the original (PDF) on 19 July 2011.
  37. ^ Kosintsev, Pavel (2010). "Relict Mammal Species of the Middle Pleistocene in Late Pleistocene Fauna of the Western Siberia South". In Titov, V.V.; Tesakov, A.S. (eds.). (PDF). Rostov-on-Don: Russian Academy of Science. pp. 78–79. Archived from the original (PDF) on 28 September 2010. Retrieved 26 March 2011.

References edit

  • Antoine, Pierre-Olivier (March 2003). "Middle Miocene elasmotheriine Rhinocerotidae from China and Mongolia: taxonomic revision and phylogenetic relationships" (PDF). Zoologica Scripta. 32 (2): 95–118. doi:10.1046/j.1463-6409.2003.00106.x. S2CID 86800130.
  • Deng, Tao; Zheng, Min (2005). "Limb Bones of Elasmotherium (Rhinocerotidae, Perissodactyla) from Nihewan (Hebei, China)" (PDF). Vertebrata PalAsiatica (in Chinese and English) (4): 110–121.
  • Hieronymus, Tobin L. (2009). . College of Arts and Sciences of Ohio University. Archived from the original on 2 October 2016. Retrieved 28 November 2018.
  • Russell, James R. (2009). "From Zoroastrian Cosmology and Armenian heresiology to the Russian novel". In Allison, Christine; Joristen-Pruschke, Anke; Wendtland, Antje (eds.). From Daēnā to Dîn: Religion, Kultur und Sprache in der iranischen Welt; Festschrift für Philip Kezenbroek zum 60. Geburstag. Wiesbaden: Harrassowitz. pp. 141–208.
  • Sinon, Denis (1960). "Sur les noms altaïque de la licorne" (PDF). Wiener Zeitschrift für der Kunde des Morgenlandes (in French) (56): 168–176.
  • Shvyreva, A.K. (2016). Эласмотерии плейстоцена Евразии (in Russian). Печатный Двор, Ставрополь.

External links edit

  • Piper, Ross (2010). "Elasmotherium and the case of the massive horn". Scrubmuncher's Blog. Nature Blog Network. Retrieved 30 August 2013.
  • Strauss, Bob. . Dinosaurs at About.com. About.com. Archived from the original on 11 November 2016. Retrieved 30 August 2013.

elasmotherium, extinct, genus, large, rhinoceros, endemic, eurasia, during, late, miocene, through, late, pleistocene, with, youngest, reliable, dates, around, years, last, surviving, member, elasmotheriinae, distinctive, group, rhinoceroses, separate, from, g. Elasmotherium is an extinct genus of large rhinoceros endemic to Eurasia during Late Miocene through to the Late Pleistocene with the youngest reliable dates around 39 000 years ago It was the last surviving member of Elasmotheriinae a distinctive group of rhinoceroses separate from the group that contains living rhinoceros Rhinocerotinae 2 ElasmotheriumTemporal range Late Miocene to Late Pleistocene 7 0 039 Ma PreꞒ Ꞓ O S D C P T J K Pg NReconstructed E caucasicum skeleton Azov Museum of History Archaeology and PalaeontologyScientific classificationDomain EukaryotaKingdom AnimaliaPhylum ChordataClass MammaliaOrder PerissodactylaFamily RhinocerotidaeSubfamily ElasmotheriinaeGenus ElasmotheriumJ Fischer 1808 1 Type species Elasmotherium sibiricumOther Species E caucasicum E chaprovicum E peii E primigeniumApproximate range map for ElasmotheriumSynonymsStereoceros Enigmatherium E fischeri E sibiricum E inexpectatum E caucasicumFive species are recognised The genus first appeared in the Late Miocene in present day China likely having evolved from Sinotherium before spreading to the Pontic Caspian steppe the Caucasus and Central Asia 3 The best known Elasmotherium species E sibiricum sometimes called the Siberian unicorn 4 was the size of a mammoth and is often conjectured to have borne a single very large horn However no horn has ever been found and other authors have conjectured that the horn was likely much smaller Like all rhinoceroses elasmotheres were herbivorous Unlike any other rhinos and any other ungulates aside from some notoungulates its high crowned molars were ever growing and it was likely adapted for a grazing diet Its legs were longer than those of other rhinos and were adapted for galloping giving it a horse like gait Contents 1 Taxonomy 1 1 Evolution 1 2 Species 2 Description 2 1 Dentition 2 2 Horn 3 Palaeobiology 3 1 Diet 3 2 Movement 3 3 Extinction 4 See also 5 Notes 6 References 7 External linksTaxonomy edit nbsp The Moscow mandible holotype of E sibiricumElasmotherium was first described in 1809 by German Russian palaeontologist Gotthelf Fischer von Waldheim based on a left lower jaw four molars and the tooth root of the third premolar which was gifted to Moscow University by princess Ekaterina Dashkova in 1807 He first announced it at an 1808 presentation before the Moscow Society of Naturalists 5 The genus name derives from Ancient Greek elasmos laminated and therion beast in reference to the laminated folding of the tooth enamel and the species name sibericus is probably a reference to the predominantly Siberian origin of princess Dashkova s collection However the specimen s exact origins are unknown In 1877 German naturalist Johann Friedrich von Brandt placed it into the newly erected subfamily Elasmotheriinae separate from modern rhinos 6 In 1997 the McKenna Bell classification considered Elasmotherium to be closely related to the wooly and modern rhinos and placed it into the subfamily Rhinocerotinae A complete mitochondrial genome obtained from a specimen of E sibiricum vindicated von Brandt finding it to be the sister taxon to all living rhinoceroses with an estimated divergence time of 47 4 million years ago with a 95 highest posterior density of 41 9 53 2 Ma 2 The genus is known from hundreds of find sites mainly of cranial fragments and teeth but in some cases nearly complete skeletons of post cranial bones scattered over Eurasia from Eastern Europe to China 7 Dozens of crania have been reconstructed and given archaeological identifiers The division into species is based mainly on the fine distinctions of the teeth and jaws and the shape of the skull 8 Evolution edit Rhinoceroses are divided into two subfamilies Rhinocerotinae and Elasmotheriinae which diverged perhaps 47 3 mya 35 mya at the latest 2 Elasmotherium is the only known member of the latter from after the Miocene others becoming extinct with the expansion of savannas 9 The oldest known species of Elasmotherium is Elasmotherium primigenium from the Late Miocene of Dingbian County in Shaanxi China Elasmotherium likely evolved from Sinotherium a genus of elasmothere also found in China 10 Elasmotherium arrived in Eastern Europe around 2 5 million years ago during the earliest part of the Pleistocene epoch 11 Hypsodonty a dentition pattern where the molars have high crowns and the enamel extends below the gum line is thought to be a characteristic of Elasmotheriinae 12 perhaps as an adaptation to the heavier grains featured in riparian zones on riversides 13 Species edit There are four chronospecies of Elasmotherium aside from the aforementioned E primigenium which are from oldest to youngest E chaprovicum E peii E caucasicum and E sibiricum and which together span from the Late Pliocene to the Late Pleistocene 3 nbsp Skeletal reconstruction of Elasmotherium sibiricum nbsp First published restoration 1878 of E sibiricum by Rashevsky under supervision of A F BrantAn elasmotherian species turned up in the preceding Khaprovian or Khaprov Faunal Complex which was at first taken to be E caucasicum 14 and then on the basis of the dentition was redefined as a new species E chaprovicum Shvyreva 2004 named after the Khaprov Faunal Complex 8 The Khaprov is in the Middle Villafranchian MN17 which spans the Piacenzian of the Late Pliocene and the Gelasian of the Early Pleistocene of Northern Caucasus Moldova and Asia and has been dated to 2 6 2 2 Ma 15 E peii was first described by Chow 1958 for remains found in Shaanxi China 16 Additional remains from Shaanxi were described in 2018 17 The species is also known from numerous remains from the classical range of Elasmotherium some sources have considered this species to be a synonym of E caucasicum but it is currently considered distinct 3 it is found during the Psekups faunal complex between 2 2 and 1 6 Ma 3 E caucasicum was first described by Russian palaeontologist Aleksei Borissiak in 1914 who said it apparently flourished in the Black Sea region as a member of the Early Pleistocene Tamanian Faunal Unit 1 1 0 8 Ma Taman Peninsula It is the most commonly found mammal of the assemblage E caucasicum is thought to be more primitive than E sibiricum and perhaps represents an ancestral stock 18 19 It is also known in northern China from the Early Pleistocene Nihewan Faunal assemblage and were extinct at approximately 1 6 Ma This suggests Elasmotherium developed separately in Russia and China 13 nbsp Paleolithic art from Rouffignac Cave France interpreted as Elasmotherium 6 E sibiricum described by Johann Fischer von Waldheim in 1808 and chronologically the latest species of the sequence appeared in the Middle Pleistocene ranging from southwestern Russia to western Siberia and southward into Ukraine and Moldova 20 Description editElasmotherium is typically reconstructed as a woolly animal generally based on the woolliness exemplified in contemporary megafauna such as mammoths and the woolly rhino However it is sometimes depicted as bare skinned like modern rhinos In 1948 Russian palaeontologist Valentin Teryaev suggested it was semi aquatic with a dome like horn and resembled a hippo because the animal had 4 toes like a wetland tapir rather than the 3 toes in other rhinos but Elasmotherium has since been shown to have had only 3 functional toes 6 and Teryaev s reconstruction has not garnered much scientific attention 6 13 The known specimens of E sibiricum reach up to 4 5 m 15 ft in length with shoulder heights up to 2 5 m 8 ft 2 in while E caucasicum reaches at least 5 m 16 ft in body length with an estimated mass of 3 5 5 tonnes 3 9 5 5 short tons 6 21 making Elasmotherium the largest rhinos of the Quaternary 2 Both species were among the largest rhinos comparable in size to the woolly mammoth and larger than the contemporary woolly rhinoceros 22 9 The feet were unguligrade the front larger than the rear with 3 digits at the front and rear with a vestigial fifth metacarpal 23 Dentition edit nbsp Size of Elasmotherium light grey compared to a human and other rhinos nbsp E caucasicum reconstructed without hair nbsp E sibiricum skull cast at the Museum fur Naturkunde BerlinLike other rhinos Elasmotherium had two premolars and three molars for chewing and lacked incisors and canines relying instead on a prehensile lip to strip food 6 Elasmotherium were euhypsodonts with large tooth crowns and enamel extending below the gum line and continuously growing teeth Elasmotherium fossils rarely show evidence of tooth roots citation needed Horn edit Elasmotherium is traditionally thought to have had a keratinous horn indicated by a circular dome on the forehead with a 13 centimetre 5 inch deep furrowed surface and a circumference of 90 cm 3 feet The furrows are interpreted as the seats of blood vessels for horn generating tissue 24 25 nbsp Restoration of E sibiricumIn rhinos the horn is not attached to bone but grows from the surface of a dense skin tissue anchoring itself by creating bone irregularities and rugosities 26 The outermost layer cornifies 27 As the layers age the horn loses diameter by degradation of the keratin due to ultraviolet light drying out and continual wearing 28 However melanin and calcium deposits in the centre harden the keratin there which gives the horn its distinctive shape 29 There was likely a large hump of muscle on the back which is generally thought to have supported a heavy horn 30 A 2021 study challenges assumptions of Elasmotherium having had a horn by comparing its cranial dome and neck musculature to those of modern rhinos The study finds that both are ill suited for a large horn and more likely are indicative of a smaller horn and that the dome could function as a resonating chamber of some sort akin to that of Rusingoryx and hadrosaur crests 31 Palaeobiology editDiet edit nbsp Restoration of E sibiricum in a steppe environmentModern hypsodont hoofed mammals are generally grazers of open environments 32 with hypsodonty possibly an adaptation to chewing tough fibrous grass 33 Elasmotherium dental wearing is similar to that of the grazing white rhino 34 and both of their heads have a downward orientation indicating a similar lifestyle and an ability to only reach low lying plants In fact the head of Elasmotherium had the most obtuse angle of any rhinoceros and could only reach the lowest levels and therefore must have grazed habitually 25 Elasmotherium also displays euhypsodonty which is typically seen in rodents 35 and dental physiology could have been influenced by pulling up food from moist grainy soil Therefore they may have inhabited both mammoth steppeland and riparian riversides similar to contemporary mammoths 13 Movement edit Elasmotherium had similar running limbs to the white rhinoceros which run at 30 km h 19 mph with a top speed of 40 45 km h 25 28 mph However Elasmotherium had double the weight about 5 t 5 5 short tons and consequently had a more restricted gait and mobility likely achieving much slower speeds Elephants weighing 2 5 11 t 2 8 12 1 short tons cannot exceed a speed of 20 km h 12 mph 36 Extinction edit Elasmotherium was previously thought to have gone extinct around 200 000 years ago as part of normal extinction 2 but E sibiricum skull fragments from the Pavlodar Region Kazakhstan shows its persistence in the Western Siberian Plain about 36 000 35 000 years ago 2 Isolated remains dating to 50 000 years ago are known from the Siberian Smelovskaya and Batpak Caves likely dragged there by a predator 37 This timing is roughly coincident with the Pleistocene extinction during which many mammal species with body weights gt 45 kg died out This coincided with a shift to a cooler climate which resulted in replacement of grasses and herbs by lichens and mosses and the migration of modern humans into the area 2 See also edit nbsp Paleontology portal nbsp Prehistoric mammals portalAegyrcitherium Bugtirhinus Hispanotherium Sinotherium CoelodontaNotes edit Elasmotherium PaleoBiology Database Basic info National Center for Ecological Analysis and Synthesis 2000 Retrieved 23 March 2011 a b c d e f g Kosintsev P Mitchell K J Deviese T van der Plicht J Kuitems M Petrova E Tikhonov A Higham T Comeskey D Turney C Cooper A van Kolfschoten T Stuart A J Lister A M 2019 Evolution and extinction of the giant rhinoceros Elasmotherium sibiricum sheds light on late Quaternary megafaunal extinctions Nature Ecology amp Evolution 3 1 31 38 doi 10 1038 s41559 018 0722 0 hdl 11370 78889dd1 9d08 40f1 99a4 0e93c72fccf3 PMID 30478308 S2CID 53726338 a b c d Schvyreva A K August 2015 On the importance of the representatives of the genus Elasmotherium Rhinocerotidae Mammalia in the biochronology of the Pleistocene of Eastern Europe Quaternary International 379 128 134 Bibcode 2015QuInt 379 128S doi 10 1016 j quaint 2015 03 052 Kosintsev Pavel et al 2019 Evolution and extinction of the giant rhinoceros Elasmotherium sibiricum sheds light on late Quaternary megafaunal extinctions Nature Ecology and Evolution 3 1 31 38 doi 10 1038 s41559 018 0722 0 hdl 11370 78889dd1 9d08 40f1 99a4 0e93c72fccf3 PMID 30478308 S2CID 53726338 Fischer G 1809 Sur L Elasmotherium et le Trogontotherium Memoires de la Societe des naturalistes de Moscou Moscow Imprimerie de l Universite Imperiale 2 250 268 a b c d e f Zhegallo V Kalandadze N Shapovalov A Bessudnova Z Noskova N Tesakova E 2005 On the fossil rhinoceros Elasmotherium including the collections of the Russian Academy of Sciences PDF Cranium 22 1 17 40 Tleuberdina Piruza Nazymbetova Gulzhan 2010 Distribution of Elasmotherium in Kazakhstan In Titov V V Tesakov A S eds Quaternary stratigraphy and paleontology of the Southern Russia connections between Europe Africa and Asia Abstracts of the International INQUA SEQS Conference Rostov on Don June 21 26 2010 PDF Rostov on Don Russian Academy of Science pp 171 173 Archived from the original PDF on 28 September 2010 Retrieved 26 March 2011 a b Titov V V 2008 Late Pliocene large mammals from Northeastern Sea of Azov Region PDF in Russian and English Rostov on Don SSC RAS Publishing a b Cerdeno Esperenza 1998 Diversity and evolutionary trends of the Family Rhinocerotidae Perissodactyla PDF Palaeo 141 1 2 13 34 Bibcode 1998PPP 141 13C doi 10 1016 S0031 0182 98 00003 0 Sun Danhui Deng Tao Jiangzuo Qigao 26 April 2021 The most primitive Elasmotherium Perissodactyla Rhinocerotidae from the Late Miocene of northern China Historical Biology 34 2 201 211 doi 10 1080 08912963 2021 1907368 ISSN 0891 2963 S2CID 235558419 Schvyreva A K 27 August 2015 On the importance of the representatives of the genus Elasmotherium Rhinocerotidae Mammalia in the biochronology of the Pleistocene of Eastern Europe Quaternary International 379 128 134 Bibcode 2015QuInt 379 128S doi 10 1016 j quaint 2015 03 052 Antoine 2003 p 109 a b c d Noskova N G 2001 Elasmotherians evolution distribution and ecology In Cavarretta G Gioia P Mussi M et al eds The World of Elephants PDF Roma Consiglio Nazionale delle Ricerche pp 126 128 ISBN 978 88 8080 025 5 Logvynenko Vitaliy The Development of the Late Pleistocene to Early Middle Pleistocene Large Mammal Fauna of Ukraine PDF 18th International Senckenberg Conference 2004 in Weimar Abstracts Senckenberg Gesellschaft fur Naturforschung SGN Bajgusheva Vera S Titov Vadim V Results of the Khapry Faunal Unit revision PDF 18th International Senckenberg Conference 2004 in Weimar Abstracts Senckenberg Gesellschaft fur Naturforschung SGN Chow M C 1958 New elasmotherine Rhinoceroses from Shansi Vertebrato PalA siatica 2 135 142 Tong Hao wen Chen Xi Zhang Bei 1 September 2018 New postcranial bones of elasmotherium peii from shanshenmiaozui in Nihewan basin Northern China Quaternaire vol 29 3 195 204 doi 10 4000 quaternaire 10010 ISSN 1142 2904 S2CID 135026963 Deng amp Zheng 2005 p 119 Deng amp Zheng 2005 p 112 Baigusheva Vera Titov Vadim 2010 Pleistocene Large Mammal Associations of the Sea of Azov and Adjacent Regions In Titov V V Tesakov A S eds Quaternary stratigraphy and paleontology of the Southern Russia connections between Europe Africa and Asia Abstracts of the International INQUA SEQS Conference Rostov on Don June 21 26 2010 PDF Rostov on Don Russian Academy of Science pp 24 27 Archived from the original PDF on 28 September 2010 Retrieved 26 March 2011 Schvyreva A K 2016 Elasmoterii plejstocena Evrazii PDF in Russian pp 103 105 Cerdeno Esperanza Nieto Manuel 1995 Changes in Western European Rhinocerotidae related to climatic variations PDF Palaeo 114 2 4 328 Bibcode 1995PPP 114 325C doi 10 1016 0031 0182 94 00085 M Belyaeva E I 1977 About the Hyroideum Sternum and Metacarpale V Bones of Elasmotherium sibiricum Fischer Rhinocerotidae PDF Journal of the Palaeontological Society of India 20 10 15 Brandt Alexander Lockyer Norman 8 August 1878 The Elasmotherium Nature XVIII 458 287 389 Bibcode 1878Natur 18R 387 doi 10 1038 018387b0 a b van der Made Jan Grube Rene 2010 The rhinoceroses from Neumark Nord and their nutrition In Meller Harald ed Elefantenreich Eine Fossilwelt in Europa PDF Halle Saale pp 382 394 Hieronymus 2009 pp 221 223 Hieronymus 2009 p 24 Hieronymus 2009 p 27 Hieronymus 2009 p 28 Hieronymus 2009 p 36 Titov Vadim V Baigusheva Vera S Uchytel Roman S 16 November 2021 The experience in reconstructing of the head of Elasmotherium Rhinocerotidae PDF Russian Journal of Theriology 20 2 173 182 doi 10 15298 rusjtheriol 20 2 06 ISSN 1682 3559 S2CID 244138119 Mendoza M Palmqvist P February 2008 Hypsodonty in ungulates an adaptation for grass consumption or for foraging in open habitat Journal of Zoology 273 2 134 142 doi 10 1111 j 1469 7998 2007 00365 x MacFadden Bruce J 2000 Origin and evolution of the grazing guild in Cenozoic New World terrestrial mammals In Sues Hans Dieter ed Evolution of Herbivory in Terrestrial Vertebrates Perspectives from the Fossil Record Cambridge Cambridge University Press pp 226 ISBN 9780511549717 Wood Horace Elmer 2nd 1938 Causal Factors Shortening Tooth Series with Age Journal of Dental Research 17 1 1 13 doi 10 1177 00220345380170010101 S2CID 209330196 a href Template Cite journal html title Template Cite journal cite journal a CS1 maint multiple names authors list link CS1 maint numeric names authors list link von Koenigswald Wighart Goin Francisco Pascual Rosendo 1999 Hypsodonty and enamel microstructure in the Paleocene gondwanatherian mammal Sudamerica amerghinoi PDF Acta Palaeontologica Polonica 44 3 263 300 Paul Gregory S December 1998 Limb Designs Function and Running Performance in Ostrich mimics and Tyrannosaurs PDF Gaia 15 258 259 Archived from the original PDF on 19 July 2011 Kosintsev Pavel 2010 Relict Mammal Species of the Middle Pleistocene in Late Pleistocene Fauna of the Western Siberia South In Titov V V Tesakov A S eds Quaternary stratigraphy and paleontology of the Southern Russia connections between Europe Africa and Asia Abstracts of the International INQUA SEQS Conference Rostov on Don June 21 26 2010 PDF Rostov on Don Russian Academy of Science pp 78 79 Archived from the original PDF on 28 September 2010 Retrieved 26 March 2011 References editAntoine Pierre Olivier March 2003 Middle Miocene elasmotheriine Rhinocerotidae from China and Mongolia taxonomic revision and phylogenetic relationships PDF Zoologica Scripta 32 2 95 118 doi 10 1046 j 1463 6409 2003 00106 x S2CID 86800130 Deng Tao Zheng Min 2005 Limb Bones of Elasmotherium Rhinocerotidae Perissodactyla from Nihewan Hebei China PDF Vertebrata PalAsiatica in Chinese and English 4 110 121 Hieronymus Tobin L 2009 Osteological Correlates of Cephalic Skin Structures in Amniota Documenting the Evolution of Display and Feeding Structures with Fossil Data Doctoral Thesis College of Arts and Sciences of Ohio University Archived from the original on 2 October 2016 Retrieved 28 November 2018 Russell James R 2009 From Zoroastrian Cosmology and Armenian heresiology to the Russian novel In Allison Christine Joristen Pruschke Anke Wendtland Antje eds From Daena to Din Religion Kultur und Sprache in der iranischen Welt Festschrift fur Philip Kezenbroek zum 60 Geburstag Wiesbaden Harrassowitz pp 141 208 Sinon Denis 1960 Sur les noms altaique de la licorne PDF Wiener Zeitschrift fur der Kunde des Morgenlandes in French 56 168 176 Shvyreva A K 2016 Elasmoterii plejstocena Evrazii in Russian Pechatnyj Dvor Stavropol External links edit nbsp Wikimedia Commons has media related to Elasmotherium Piper Ross 2010 Elasmotherium and the case of the massive horn Scrubmuncher s Blog Nature Blog Network Retrieved 30 August 2013 Strauss Bob Elasmotherium About com Prehistoric Mammals Dinosaurs at About com About com Archived from the original on 11 November 2016 Retrieved 30 August 2013 Retrieved from https en wikipedia org w index php title Elasmotherium amp oldid 1213002859, wikipedia, wiki, book, books, library,

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