Saiga antelope

Species of antelope

Saiga antelope
Temporal range: Pleistocene–Recent
PreꞒ
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S
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C
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A male at the Stepnoi Nature Sanctuary of Astrakhan Oblast, Russia
A female at the Askania-Nova Biosphere Reserve of Kakhovka Raion, Ukraine
Conservation status

Near Threatened (IUCN 3.1)[1]
CITES Appendix II (CITES)[1]
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Artiodactyla
Family: Bovidae
Subfamily: Antilopinae
Tribe: Saigini
Genus: Saiga
Gray, 1843
Species:
S. tatarica
Binomial name
Saiga tatarica
(Linnaeus, 1766)
Subspecies
  • S. t. tatarica
  • S. t. mongolica
Reconstructed range (white) and current distribution of the two subspecies Saiga tatarica tatarica (green) and S. t. mongolica (red).
Synonyms[2]
List
  • Antilope saiga Pallas, 1766
  • Antilope scythica Pallas, 1766
  • Capra tatarica Linnaeus, 1766
  • Capra sayga Forster, 1768
  • Cemas colus Oken, 1816
  • Ibex imberbis S. G. Gmelin, 1760

The saiga antelope (/ˈsɡə/, Saiga tatarica), or saiga, is a species of antelope which during antiquity inhabited a vast area of the Eurasian steppe, spanning the foothills of the Carpathian Mountains in the northwest and Caucasus in the southwest into Mongolia in the northeast and Dzungaria in the southeast. During the Pleistocene, it ranged across the mammoth steppe from the British Isles to Beringia. Today, the dominant subspecies (S. t. tatarica) only occurs in Kalmykia and Astrakhan Oblast of Russia and in the Ural, Ustyurt and Betpak-Dala regions of Kazakhstan. A portion of the Ustyurt population migrates south to Uzbekistan and occasionally to Turkmenistan in winter. It is regionally extinct in Romania, Ukraine, Moldova, China and southwestern Mongolia. The Mongolian subspecies (S. t. mongolica) occurs only in western Mongolia.[3][4]

Taxonomy and phylogeny

The scientific name Capra tatarica was coined by Carl Linnaeus in 1766 in the 12th edition of Systema Naturae.[5] It was reclassified as Saiga tatarica and is the sole living member of the genus Saiga.[6] Two subspecies are recognised:[6][7][1]

  • S. t. tatarica (Linnaeus, 1766): also known as the Russian saiga, it occurs in central Asia.
  • S. t. mongolica Bannikov, 1946: also known as the Mongolian saiga, it is sometimes treated as an independent species, or as subspecies of the Pleistocene Saiga borealis;[1] it is confined to Mongolia.

In 1945, American paleontologist George Gaylord Simpson classified both in the tribe Saigini under the same subfamily, Caprinae. Subsequent authors were not certain about the relationship between the two, until phylogenetic studies in the 1990s revealed that though morphologically similar, the Tibetan antelope is closer to the Caprinae while the saiga is closer to the Antilopinae.[8]

In a revision of the phylogeny of the tribe Antilopini on the basis of nuclear and mitochondrial data in 2013, Eva Verena Bärmann (of the University of Cambridge) and colleagues showed that the saiga is sister to the clade formed by the springbok (Antidorcas marsupialis) and the gerenuk (Litocranius walleri).[9] The study noted that the saiga and the springbok could be considerably different from the rest of the antilopines; a 2007 phylogenetic study suggested that the two form a clade sister to the gerenuk.[10] The cladogram below is based on the 2013 study.[9]

Evolution

Saiga antelope skull and taxidermy mount on display at the Museum of Osteology

Fossils of saiga, concentrated mainly in central and northern Eurasia, date to as early as the late Pleistocene (nearly 0.1 Mya).[11] Several species of extinct Saiga from the Pleistocene of Eurasia and Alaska have been named, including S. borealis,[12] S. prisca, S. binagadensis and S. ricei, although more recent studies suggest that these prehistoric representatives were merely geographical variants of the extant species that was formerly much more widespread.[13] Fossils excavated from the Buran Kaya III site (Crimea) date back to the transition from Pleistocene to Holocene.[14] The morphology of saiga does not seem to have changed significantly since prehistoric times.[2]

Before the Holocene, the saiga ranged across the mammoth steppe from as far west as modern-day England and France to as far east as northern Siberia, Alaska, and probably Canada.[15] The antelope gradually entered the Urals, though it did not colonise southern Europe. A 2010 study revealed that a steep decline has occurred in the genetic variability of the saiga since the late Pleistocene-Holocene, probably due to a population bottleneck.[16]

Characteristics

The saiga stands 61–81 cm (24–32 in) at the shoulder, and weighs 26–69 kg (57–152 lb). The head-and-body length is typically between 100 and 140 cm (39 and 55 in). A prominent feature of the saiga is the pair of closely spaced, bloated nostrils directed downward. Other facial features include the dark markings on the cheeks and the nose, and the 7–12 cm (2.8–4.7 in) long ears.[2][17]

The coat shows seasonal changes. In summer, the coat appears yellow to red, fading toward the flanks. The Mongolian saiga can develop a sandy colour. The coat develops a pale, grayish-brown colour in winter, with a hint of brown on the belly and the neck. The ventral parts are generally white. The hairs, that measure 18–30 mm (0.71–1.18 in) long in summer, can grow as long as 40–70 mm (1.6–2.8 in) in winter. This forms a 12 to 15 cm (4.7 to 5.9 in) long mane on the neck. Two distinct moults can be observed in a year, one in spring from April to May and another in autumn from late September or early October to late November or early December. The tail measures 6–12 cm (2.4–4.7 in).[2][7]

Only males possess horns. These horns, thick and slightly translucent, are wax-coloured and show 12 to 20 pronounced rings. With a base diameter of 25–33 mm (0.98–1.30 in), the horns of the Russian saiga measure 28–38 cm (11–15 in) in length; the horns of the Mongolian saiga, however, reach a maximum length of 22 cm (8.7 in).[2][7]

Ecology and behaviour

Saigas form very large herds that graze in semideserts, steppes, grasslands, and possibly open woodlands, eating several species of plants, including some that are poisonous to other animals. They can cover long distances and swim across rivers, but they avoid steep or rugged areas. The mating season starts in November, when stags fight for the acceptance of females. The winner leads a herd of five to ten females (occasionally up to 50).[2] In springtime, mothers come together in mass to give birth.[18] Two-thirds of births are twins; the remaining third of births are single calves.[citation needed]

Herd of saiga antelope gathered at the water's edge in western Kazakhstan
Fawn hidden in the grasses

Saigas, like the Mongolian gazelles, are known for their extensive migrations across the steppes that allow them to escape natural calamities.[19] Saigas are highly vulnerable to wolves. Juveniles are targeted by foxes, steppe eagles, golden eagles, and ravens.[2]

Distribution and habitat

Antiquity

During the last glacial period, the saigas ranged from the British Isles through Central Asia and the Bering Strait into Alaska and Canada's Yukon and Northwest Territories. By the classical age, they were apparently considered a characteristic animal of Scythia, judging from the historian Strabo's description of an animal called the kolos that was "between the deer and ram in size" and was wrongly believed to drink through its nose.[20]

Considerable evidence shows the importance of the antelope to Andronovo culture settlements. Illustrations of saiga antelopes can be found among the cave paintings that were dated back to seventh to fifth century BC. Moreover, saiga bones were found among the remains of other wild animals near the human settlements.[21]

From the 14th century to the 20th century

The fragmented information shows an abundance of saigas on the territory of modern Kazakhstan in the 14th-16th centuries. The migratory routes ranged throughout the country's area, especially the region between the Volga and Ural Rivers was heavily populated.[22] The population's size remained high until the second half of the 19th century, when excessive horn export began. The high price and demand for horns drove radical hunting. The number of animals decreased in all regions and the migratory routes shifted southward.[23] Populations in Ukraine were driven to extirpation in the 18th century.[1]

After a rapid decline, they were nearly completely exterminated in the 1920s, but they were able to recover. By 1950, two million of them were found in the steppes of the USSR. Their population fell drastically following the collapse of the USSR due to uncontrolled hunting and demand for horns in Chinese medicine. At one point, some conservation groups, such as the World Wildlife Fund, encouraged the hunting of this species, as its horn was presented as an alternative to that of a rhinoceros.[24]

Present day

In the mid-2010s, the populations again shrank enormously – as much as 95% in 15 years.[25] This led the saiga to be classified as critically endangered on the IUCN Red List. In more recent years, the saiga has experienced massive regrowth. As of 2022, there is an estimated number of 1.38 million saiga surviving in Kazakhstan, per an April aerial count.[26] As of December 2023, the global saiga antelope population is estimated to number 922,600–988,500 mature individuals.[1]

Cherny Zemli Nature Reserve was created in Russia's Kalmykia Republic in the 1990s to protect the local saiga population. Kalmykia's president Kirsan Ilyumzhinov announced 2010 as the Year of Saiga in Kalmykia. In Kazakhstan, the number of saigas was found to be increasing, from around 21,000 at the beginning of this millennium to around 81,000 in January 2010.[citation needed] However, in May 2010, an estimated 12,000 of the 26,000 saiga population in the Ural region of Kazakhstan have been found dead. Although the deaths are currently being ascribed to pasteurellosis, an infectious disease that strikes the lungs and intestines, the underlying trigger remains to be identified.[27] In May 2015, what may be the same disease broke out in three northern regions of the country.[28] As of 28 May 2015, more than 120,000 saigas have been confirmed dead in the Betpak-Dala population in central Kazakhstan, representing more than a third of the global population.[29] By April 2016, the saigas appear to be making a comeback, with an increase of population from 31,000 to 36,000 in the Betpak-Dala area.[30] In April 2021 a survey in Kazakhstan found that the saiga population had risen from an estimated 334,000 to 842,000. The population increase was partially attributed to the government crackdown on poaching and the establishment of conservation areas.[31] UK charity RSPB reported in 2022 that, partly due to their conservation efforts, as well as the designation of the Bokey Orda-Ashiozek protected area by the Kazakhstan government, the population had now risen to a peak of 1.32 million.[32]

Mongolian saiga

The Mongolian saiga (S. t. mongolica) is found in a small area in western Mongolia around the Sharga and Mankhan Nature Reserves.[33]

Threats

Stuffed saiga herd at The Museum of Zoology, St. Petersburg
Examples of saiga horn products seized by the Hong Kong government

The horn of the saiga antelope is used in traditional Chinese medicine and can sell for as much as US$150. Demand for the horns drives poaching and smuggling, which has wiped out the population in China, where the saiga antelope is a class I protected species.[34]

In June 2014, Chinese customs at the Kazakh border uncovered 66 cases containing 2,351 saiga antelope horns, estimated to be worth over Y70.5 million (US$11 million).[35] In June 2015, E. J. Milner-Gulland (chair of Saiga Conservation Alliance) said: "Antipoaching needs to be a top priority for the Russian and Kazakh governments."[18]

Hunting

Saigas have been a target of hunting since prehistoric ages, when hunting was an essential means to acquire food. Saigas' horns, meat, and skin have commercial value and are exported from Kazakhstan.

Saiga horn, known as Cornu Antelopis, is one of the main ingredients in traditional Chinese medicine that is used as an extract or powder additive to the elixirs, ointments, and drinks. Saiga horn's value is equal to rhinoceros horn, whose trade was banned in 1993. Cornu Antelopis is thought to be a cheaper substitute of rare rhino horn in most TCM recipes.[36]

In the period from 1955 to 1989, over 87 thousand tonnes of meat were collected in Kazakhstan by killing more than five million saiga.[37] In 2011, Kazakhstan reaffirmed a ban on hunting saiga and extended this ban until 2021.[38]

Saiga meat is compared to lamb, considered to be nutritious and delicious. Numerous recipes for cooking the antelope's meat can be found.[39] Both meat and byproducts are sold in the country and outside of it. About 45–80 dm2 of skin can be harvested from one individual depending on its age and sex.[23]

Physical barriers

Agricultural advancement and human settlements have been shrinking habitat areas of the saigas since the 20th century.[23] Occupants limited saiga's passage to water resources and the winter and summer habitats. The ever-changing face of steppe requires saigas to search for new routes to their habitual lands. Currently, saiga populations' migratory routes pass five countries and different human-made constructions, such as railways, trenches, mining sites, and pipelines.[23] These physical barriers limit movement of the antelopes. Cases of saiga herds being trapped within fenced areas and starving to death have been reported.[40]

Climatic variability

Saigas are dependent on weather and affected by climate fluctuations to a great extent due to their migratory nature.[41] Harsh winters with strong winds or high snow coverage prevent them from feeding on the underlying grass. Population size usually dramatically decreases after severe cold months.[23] Recent trends in climate change have increased the aridity of the steppe region, leading an estimated 14% or more of available pastureland to be considered degraded and useless.[42] Concurrently, small steppe rivers dry faster, limiting water resources to large lakes and rivers, which are usually populated by human settlements; high temperatures in the steppe region lead to springtime floods, in which saiga calves can drown.[23]

Mass epizootic mortality

1980 to 2015 events

For ungulates, mass mortalities are not uncommon. In the 1980s, several saiga die-offs occurred, and between 2010 and 2014, one occurred every year. The deaths could be linked to calving aggregation, which is when they are most vulnerable.[18] More recent research involving a mass die-off in 2015 indicates warmer weather and attendant humidity led bacteria common in saiga antelopes to move into the bloodstream and cause hemorrhagic septicemia.[43]

2015–2016 epizootic

In May 2015, uncommonly large numbers of saigas began to die from a mysterious epizootic illness suspected to be pasteurellosis.[18][44] Herd fatality is 100% once infected, with an estimated 40% of the species' total population already dead.[45] More than 120,000 carcasses had been found by late May 2015, while the estimated total population was only 250,000.[46]

Biologist Murat Nurushev suggested that the cause might be acute ruminal tympany, whose symptoms (bloating, mouth foaming, and diarrhea) had been observed in dead saiga antelopes.[47] According to Nurushev, this disease occurred as a result of foraging on a large amount of easily fermenting plants (alfalfa, clover, sainfoins, and mixed wet, green grass).[47] In May 2015, the United Nations agency which is involved in saiga conservation efforts issued a statement that the mass die-off had ended.[citation needed] By June 2015, no definitive cause for the epizootic had been found.[48]

At a scientific meeting in November 2015 in Tashkent, Uzbekistan, Dr. Richard A. Kock (of the Royal Veterinary College in London) reported that his colleagues and he had narrowed down the possible culprits. Climate change and stormy spring weather, they said, may have transformed harmless bacteria, carried by the saigas, into lethal pathogens.[49]

Pasteurella multocida, a bacterium, was determined to be the cause of death. The bacterium occurs in the antelopes and is normally harmless; the reason for the change in behavior of the bacterium is unknown.[50]

Now, scientists and researchers believe the unusually warm and wet uncontrolled environmental variables caused the bacterium to enter the bloodstream and become septic. Hemorrhagic septicemia is the likely cause of the most recent deaths[51] The change of the bacteria may be attributed to "the response of opportunistic microbes to changing environmental conditions".[52]

The Betpak-Dala saiga population in central Kazakhstan, which saw the most deaths, increased from 31,000 after the epidemic to 36,000 by April 2016.[50]

In late 2016, a large loss of the population happened in Mongolia. The etiology was confirmed to be goat plague in early 2017.[53]

Conservation

Under the auspices of the Convention on the Conservation of Migratory Species of Wild Animals, the Saiga Antelope Memorandum of Understanding was concluded and came into effect on 24 September 2006.[54]

In captivity

Currently, only the Almaty Zoo and Askania-Nova keep saigas.[55]

References

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Further reading

  • Singh, N.J.; Milner-Gulland, E.J. (2011). "Conserving a moving target: planning protection for a migratory species as its distribution changes" (PDF). Journal of Applied Ecology. 48: 35–46. doi:10.1111/j.1365-2664.2010.01905.x.
  • Singh, N.J.; Grachev, Iu.A.; Bekenov, A.B.; Milner-Gulland, E.J. (2010). "Tracking greenery in Central Asia: The migration of the saiga antelope". Diversity and Distributions. 16 (4): 663–675. doi:10.1111/j.1472-4642.2010.00671.x. S2CID 83904273.
  • Singh, N.J.; Grachev, Iu.A.; Bekenov, A.B.; Milner-Gulland, E.J. (2010). "Saiga antelope calving site selection is increasingly driven by human disturbance". Biological Conservation. 143 (7): 1770–1779. doi:10.1016/j.biocon.2010.04.026.
  • Kuhl, A.; Mysterud, A.; Grachev, Iu.A.; Bekenov, A.B.; Ubushaev, B.S.; Lushchekina, A.A.; Milner-Gulland, E.J. (2009). "Monitoring population productivity in the saiga antelope". Animal Conservation. 12 (4): 355–363. doi:10.1111/j.1469-1795.2009.00260.x. S2CID 86008409.
  • Kuhl, A.; Balinova, N.; Bykova, E.; Esipov, A.; Arylov, Iu.A.; Lushchekina, A.A.; Milner-Gulland, E.J. (2009). "The role of saiga poaching in rural communities: Linkages between attitudes, socio-economic circumstances and behaviour". Biological Conservation. 142 (7): 1442–1449. doi:10.1016/j.biocon.2009.02.009.
  • Kuhl, A.; Mysterud, A.; Erdnenov, G.I.; Lushchekina, A.A.; Grachev, Iu. A.; Bekenov, A.B.; Milner-Gulland, E.J. (2007). "The big spenders of the steppe: sex-specific maternal allocation and twinning in the saiga antelope". Proceedings of the Royal Society B. 274 (1615): 1293–1299. doi:10.1098/rspb.2007.0038. PMC 2176182. PMID 17341456..
  • Morgan, E.R.; Medley, G.F.; Torgerson, P.R.; Shaikenov, B. & Milner-Gulland, E.J. (2007). "Parasite transmission in a migratory multiple host system". Ecological Modelling. 200 (3–4): 511–520. doi:10.1016/j.ecolmodel.2006.09.002.
  • Kholodova, M.V.; Milner-Gulland, E.J.; Easton, A.J.; Amgalan, L.; Arylov, Iu.; Bekenov, A.; Grachev, Iu.A.; Lushchekina, A.A.; Ryder, O. (2006). "Mitochondrial DNA variation and population structure of the Critically Endangered saiga antelope Saiga tatarica". Oryx. 40: 103–107. doi:10.1017/S0030605306000135.
  • Morgan, E.R.; Lundervold, M.; Medley, G.F.; Shaikenov, B.S.; Torgerson, P.R.; Milner-Gulland, E.J. (2006). "Assessing risks of disease transmission between wildlife and livestock: the Saiga antelope as a case study". Biological Conservation. 131 (2): 244–254. doi:10.1016/j.biocon.2006.04.012.
  • Morgan, E.R.; Shaikenov, B.; Torgerson, P.R.; Medley, G.F.; Milner-Gulland, E.J. (2005). "Helminths of saiga antelopes in Kazakhstan: Implications for conservation and livestock production". Journal of Wildlife Diseases. 41 (1): 149–162. doi:10.7589/0090-3558-41.1.149. PMID 15827221. S2CID 22806238.
  • Milner-Gulland, E.J.; Bukreeva, O.M.; Coulson, T.N.; Lushchekina, A.A.; Kholodova, M.V.; Bekenov, A.B.; Grachev, Iu.A. (2003). "Reproductive collapse in saiga antelope harems". Nature. 422 (6928): 135. doi:10.1038/422135a. PMID 12634775. S2CID 4409236.
  • Robinson, S.; Milner-Gulland, E.J. (2003). "Political change and factors limiting numbers of wild and domestic ungulates in Kazakhstan". Human Ecology. 31: 87–110. doi:10.1023/A:1022834224257. S2CID 67810286.
  • Milner-Gulland, E.J.; Kholodova, M.V.; Bekenov, A.B.; Bukreeva, O.M.; Grachev, Iu.A.; Amgalan, L.; Lushchekina, A.A. (2001). "Dramatic declines in saiga antelope populations". Oryx. 35 (4): 340–345. doi:10.1046/j.1365-3008.2001.00202.x.

External links

Wikimedia Commons has media related to Saiga antelope.
  • CMS Saiga Memorandum of Understanding
  • saiga-antelope/saiga-tatarica Saiga antelope media from ARKive Edit this at Wikidata
  • Ultimate Ungulate
  • WWF species profile: Saiga antelope
  • "IFAW Russia – Saiga antelopes are rare creatures". YouTube. 3 July 2012. Archived from the original on 21 December 2021.
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Extant Artiodactyla species
Suborder Ruminantia
Antilocapridae
Antilocapra
  • Pronghorn (A. americana)
Giraffidae
Okapia
  • Okapi (O. johnstoni)
Giraffa
  • Northern giraffe (G. camelopardalis)
  • Southern giraffe (G. giraffa)
  • Reticulated giraffe (G. reticulata)
  • Masai giraffe (G. tippelskirchi)
Moschidae
Moschus
  • Anhui musk deer (M. anhuiensis)
  • Dwarf musk deer (M. berezovskii)
  • Alpine musk deer (M. chrysogaster)
  • Kashmir musk deer (M. cupreus)
  • Black musk deer (M. fuscus)
  • Himalayan musk deer (M. leucogaster)
  • Siberian musk deer (M. moschiferus)
Tragulidae
Hyemoschus
  • Water chevrotain (H. aquaticus)
Moschiola
  • Indian spotted chevrotain (M. indica)
  • Yellow-striped chevrotain (M. kathygre)
  • Sri Lankan spotted chevrotain (M. meminna)
Tragulus
  • Java mouse-deer (T. javanicus)
  • Lesser mouse-deer (T. kanchil)
  • Greater mouse-deer (T. napu)
  • Philippine mouse-deer (T. nigricans)
  • Vietnam mouse-deer (T. versicolor)
  • Williamson's mouse-deer (T. williamsoni)
Cervidae
Large family listed below
Bovidae
Large family listed below
Family Cervidae
Cervinae
Muntiacus
  • Bornean yellow muntjac (M. atherodes)
  • Hairy-fronted muntjac (M. crinifrons)
  • Fea's muntjac (M. feae)
  • Gongshan muntjac (M. gongshanensis)
  • Sumatran muntjac (M. montanus)
  • Southern red muntjac (M. muntjak)
  • Pu Hoat muntjac (M. puhoatensis)
  • Leaf muntjac (M. putaoensis)
  • Reeves's muntjac (M. reevesi)
  • Roosevelt's muntjac (M. rooseveltorum)
  • Truong Son muntjac (M. truongsonensis)
  • Northern red muntjac (M. vaginalis)
  • Giant muntjac (M. vuquangensis)
Elaphodus
  • Tufted deer (E. cephalophus)
Dama
  • European fallow deer (D. dama)
  • Persian fallow deer (D. mesopotamica)
Axis
  • Chital (A. axis)
  • Calamian deer (A. calamianensis)
  • Bawean deer (A. kuhlii)
  • Hog deer (A. porcinus)
Rucervus
  • Barasingha (R. duvaucelii)
  • Eld's deer (R. eldii)
Elaphurus
  • Père David's deer (E. davidianus)
Rusa
  • Visayan spotted deer (R. alfredi)
  • Philippine sambar (R. mariannus)
  • Rusa deer (R. timorensis)
  • Sambar (R. unicolor)
Cervus
  • Thorold's deer (C. albirostris)
  • Red deer (C. elaphus)
  • Elk (C. canadensis)
  • Central Asian red deer (C. hanglu)
  • Sika deer (C. nippon)
Capreolinae
Alces
  • Moose (A. alces)
Hydropotes
  • Water deer (H. inermis)
Capreolus
  • European roe deer (C. capreolus)
  • Siberian roe deer (C. pygargus)
Rangifer
  • Reindeer (R. tarandus)
Hippocamelus
  • Taruca (H. antisensis)
  • South Andean deer (H. bisulcus)
Mazama
  • Red brocket (M. americana)
  • Small red brocket (M. bororo)
  • Merida brocket (M. bricenii)
  • Dwarf brocket (M. chunyi)
  • Gray brocket (M. gouazoubira)
  • Pygmy brocket (M. nana)
  • Amazonian brown brocket (M. nemorivaga)
  • Little red brocket (M. rufina)
  • Central American red brocket (M. temama)
Ozotoceros
  • Pampas deer (O. bezoarticus)
Blastocerus
  • Marsh deer (B. dichotomus)
Pudu
  • Northern pudu (P. mephistophiles)?
  • Southern pudu (P. pudu)
Pudella?
  • Peruvian Yungas pudu (P. carlae)
  • Northern pudu (P. mephistophiles)
Odocoileus
  • Mule deer (O. hemionus)
  • Yucatan brown brocket (O. pandora)
  • White-tailed deer (O. virginianus)
Family Bovidae
Hippotraginae
Hippotragus
  • Roan antelope (H. equinus)
  • Sable antelope (H. niger)
Oryx
  • East African oryx (O. beisa)
  • Scimitar oryx (O. dammah)
  • Gemsbok (O. gazella)
  • Arabian oryx (O. leucoryx)
Addax
  • Addax (A. nasomaculatus)
Reduncinae
Kobus
  • Waterbuck (K. ellipsiprymnus)
  • Kob (K. kob)
  • Lechwe (K. leche)
  • Nile lechwe (K. megaceros)
  • Puku (K. vardonii)
Redunca
  • Southern reedbuck (R. arundinum)
  • Mountain reedbuck (R. fulvorufula)
  • Bohor reedbuck (R. redunca)
Aepycerotinae
Aepyceros
  • Impala (A. melampus)
Peleinae
Pelea
  • Grey rhebok (P. capreolus)
Alcelaphinae
Beatragus
  • Hirola (B. hunteri)
Damaliscus
  • Common tsessebe (D. lunatus)
  • Bontebok (D. pygargus)
Alcelaphus
  • Hartebeest (A. buselaphus)
Connochaetes
  • Black wildebeest (C. gnou)
  • Blue wildebeest (C. taurinus)
Pantholopinae
Pantholops
  • Tibetan antelope (P. hodgsonii)
Caprinae
Large subfamily listed below
Bovinae
Large subfamily listed below
Antilopinae
Large subfamily listed below
Family Bovidae (subfamily Caprinae)
Ammotragus
  • Barbary sheep (A. lervia)
Arabitragus
  • Arabian tahr (A. jayakari)
Budorcas
  • Takin (B. taxicolor)
Capra
  • Wild goat (C. aegagrus)
  • West Caucasian tur (C. caucasia)
  • East Caucasian tur (C. cylindricornis)
  • Markhor (C. falconeri)
  • Domestic goat (C. hircus)
  • Alpine ibex (C. ibex)
  • Nubian ibex (C. nubiana)
  • Iberian ibex (C. pyrenaica)
  • Siberian ibex (C. sibirica)
  • Walia ibex (C. walie)
Capricornis
  • Japanese serow (C. crispus)
  • Red serow (C. rubidus)
  • Mainland serow (C. sumatraensis)
  • Taiwan serow (C. swinhoei)
Hemitragus
  • Himalayan tahr (H. jemlahicus)
Naemorhedus
  • Red goral (N. baileyi)
  • Long-tailed goral (N. caudatus)
  • Himalayan goral (N. goral)
  • Chinese goral (N. griseus)
Oreamnos
  • Mountain goat (O. americanus)
Ovibos
  • Muskox (O. moschatus)
Nilgiritragus
  • Nilgiri tahr (N. hylocrius)
Ovis
  • Argali (O. ammon)
  • Domestic sheep (O. aries)
  • Bighorn sheep (O. canadensis)
  • Dall sheep (O. dalli)
  • Mouflon (O. gmelini)
  • Snow sheep (O. nivicola)
  • Urial (O. vignei)
Pseudois
  • Bharal (P. nayaur)
Rupicapra
  • Pyrenean chamois (R. pyrenaica)
  • Chamois (R. rupicapra)
Family Bovidae (subfamily Bovinae)
Boselaphini
Tetracerus
  • Four-horned antelope (T. quadricornis)
Boselaphus
  • Nilgai (B. tragocamelus)
Bovini
Bubalus
  • Wild water buffalo (B. arnee)
  • Domestic water buffalo (B. bubalis)
  • Lowland anoa (B. depressicornis)
  • Tamaraw (B. mindorensis)
  • Mountain anoa (B. quarlesi)
Bos
  • American bison (B. bison)
  • European bison (B. bonasus)
  • Bali cattle (B. domesticus)
  • Gayal (B. frontalis)
  • Gaur (B. gaurus)
  • Domestic yak (B. grunniens)
  • Zebu (B. indicus)
  • Banteng (B. javanicus)
  • Wild yak (B. mutus)
  • Cattle (B. taurus)
Pseudoryx
  • Saola (P. nghetinhensis)
Syncerus
  • African buffalo (S. caffer)
Tragelaphini
Tragelaphus
(including kudus)
  • Nyala (T. angasii)
  • Mountain nyala (T. buxtoni)
  • Bongo (T. eurycerus)
  • Lesser kudu (T. imberbis)
  • Harnessed bushbuck (T. scriptus)
  • Sitatunga (T. spekeii)
  • Greater kudu (T. strepsiceros)
  • Cape bushbuck (T. sylvaticus)
Taurotragus
  • Giant eland (T. derbianus)
  • Common eland (T. oryx)
Family Bovidae (subfamily Antilopinae)
Antilopini
Ammodorcas
  • Dibatag (A. clarkei)
Antidorcas
  • Springbok (A. marsupialis)
Antilope
  • Blackbuck (A. cervicapra)
Eudorcas
  • Mongalla gazelle (E. albonotata)
  • Red-fronted gazelle (E. rufifrons)
  • Thomson's gazelle (E. thomsonii)
  • Heuglin's gazelle (E. tilonura)
Gazella
  • Chinkara (G. bennettii)
  • Cuvier's gazelle (G. cuvieri)
  • Dorcas gazelle (G. dorcas)
  • Erlanger's gazelle (G. erlangeri)
  • Mountain gazelle (G. gazella)
  • Rhim gazelle (G. leptoceros)
  • Speke's gazelle (G. spekei)
  • Goitered gazelle (G. subgutturosa)
Litocranius
  • Gerenuk (L. walleri)
Nanger
  • Dama gazelle (N. dama)
  • Grant's gazelle (N. granti)
  • Bright's gazelle (N. notatus)
  • Peter's gazelle (N. petersii)
  • Soemmerring's gazelle (N. soemmerringii)
Procapra
  • Mongolian gazelle (P. gutturosa)
  • Goa (P. picticaudata)
  • Przewalski's gazelle (P. przewalskii)
Saigini
Pantholops
  • Tibetan antelope (P. hodgsonii)
Saiga
  • Saiga antelope (S. tatarica)
Neotragini
Dorcatragus
  • Beira (D. megalotis)
Madoqua
  • Günther's dik-dik (M. guentheri)
  • Kirk's dik-dik (M. kirkii)
  • Silver dik-dik (M. piacentinii)
  • Salt's dik-dik (M. saltiana)
Neotragus
  • Bates' pygmy antelope (N. batesi)
  • Suni (N. moschatus)
  • Royal antelope (N. pygmaeus)
Oreotragus
  • Klipspringer (O. oreotragus)
Ourebia
  • Oribi (O. ourebi)
Raphicerus
  • Steenbok (R. campestris)
  • Cape grysbok (R. melanotis)
  • Sharpe's grysbok (R. sharpei)
Cephalophini
Cephalophus
  • Aders's duiker (C. adersi)
  • Brooke's duiker (C. brookei)
  • Peters' duiker (C. callipygus)
  • White-legged duiker (C. crusalbum)
  • Bay duiker (C. dorsalis)
  • Harvey's duiker (C. harveyi)
  • Jentink's duiker (C. jentinki)
  • White-bellied duiker (C. leucogaster)
  • Red forest duiker (C. natalensis)
  • Black duiker (C. niger)
  • Black-fronted duiker (C. nigrifrons)
  • Ogilby's duiker (C. ogilbyi)
  • Ruwenzori duiker (C. rubidis)
  • Red-flanked duiker (C. rufilatus)
  • Yellow-backed duiker (C. silvicultor)
  • Abbott's duiker (C. spadix)
  • Weyns's duiker (C. weynsi)
  • Zebra duiker (C. zebra)
Philantomba
  • Blue duiker (P. monticola)
  • Maxwell's duiker (P. maxwellii)
  • Walter's duiker (P. walteri)
Sylvicapra
  • Common duiker (S. grimmia)
Suborder Suina
Suidae
Babyrousa
  • Buru babirusa (B. babyrussa)
  • North Sulawesi babirusa (B. celebensis)
  • Togian babirusa (B. togeanensis)
Hylochoerus
  • Giant forest hog (H. meinertzhageni)
Phacochoerus
  • Desert warthog (P. aethiopicus)
  • Common warthog (P. africanus)
Porcula
  • Pygmy hog (P. salvania)
Potamochoerus
  • Bushpig (P. larvatus)
  • Red river hog (P. porcus)
Sus
  • Palawan bearded pig (S. ahoenobarbus)
  • Bornean bearded pig (S. barbatus)
  • Visayan warty pig (S. cebifrons)
  • Celebes warty pig (S. celebensis)
  • Domestic pig (S. domesticus)
  • Flores warty pig (S. heureni)
  • Oliver's warty pig (S. oliveri)
  • Philippine warty pig (S. philippensis)
  • Wild boar (S. scrofa)
  • Timor warty pig (S. timoriensis)
  • Javan warty pig (S. verrucosus)
Tayassuidae
Tayassu
  • White-lipped peccary (T. pecari)
Catagonus
  • Chacoan peccary (C. wagneri)
Dicotyles
  • Collared peccary (D. tajacu)
Suborder Tylopoda
Camelidae
Lama
  • Llama (L. glama)
  • Guanaco (L. guanicoe)
  • Alpaca (L. pacos)
  • Vicuña (L. vicugna)
Camelus
  • Domestic Bactrian camel (C. bactrianus)
  • Dromedary/Arabian camel (C. dromedarius)
  • Wild Bactrian camel (C. ferus)
Suborder Whippomorpha
Hippopotamidae
Hippopotamus
  • Hippopotamus (H. amphibius)
Choeropsis
  • Pygmy hippopotamus (C. liberiensis)
Cetacea
  • see Cetacea
Taxon identifiers
Saiga tatarica
Capra tatarica
Authority control databases: National Edit this at Wikidata
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