Nycticebus kayan

This page is about a species that has been called Bornean slow loris. For the present-day Bornean slow loris, see Nycticebus borneanus. For other slow lorises of Borneo, see Bornean slow loris (disambiguation).
Kayan River slow loris[1]
Not evaluated (IUCN 3.1)
CITES Appendix I (CITES)[2]
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Primates
Suborder: Strepsirrhini
Family: Lorisidae
Genus: Nycticebus
Species: N. kayan
Binomial name
Nycticebus kayan
Munds, Nekaris & Ford, 2013

The Kayan River slow loris (Nycticebus kayan) is a strepsirrhine primate and a species of slow loris that is native to the northern and central highland region of the island of Borneo. The species was originally thought to be a part of the Bornean slow loris (N. menagensis) population until 2013, when a study of museum specimens and photographs identified distinct facial markings, which helped to differentiate it. It is distinguished by the high contrast of its black and white facial features, as well as the shape and width of the stripes of its facial markings.

The species is named after the Kayan River, which runs through its native habitat. As with other slow lorises, this arboreal and nocturnal species primarily eats insects, tree gum, nectar, and fruit and has a toxic bite, a unique feature among primates. Although not yet evaluated by the International Union for Conservation of Nature (IUCN), it is likely to be listed as "Vulnerable" or placed in a higher-risk category when its conservation status is assessed. It is primarily threatened by habitat loss and the illegal wildlife trade.

Taxonomy and phylogeny

N. kayan is a strepsirrhine primate, and species of slow loris (genus Nycticebus) within the family Lorisidae. Museum specimens of this animal had previously been identified as the Bornean slow loris (Nycticebus menagensis), first described by the English naturalist Richard Lydekker in 1893 as Lemur menagensis.[3] In 1953, all of the slow lorises were lumped together into a single species, the Sunda slow loris (Nycticebus coucang).[4] In 1971, that view was refined by distinguishing the pygmy slow loris (N. pygmaeus) as a species, and by further identifying four subspecies, including N. coucang menagensis, the Bornean slow loris.[5][6] The Bornean slow loris was elevated to the species level (as N. menagensis) in 2006, when molecular analysis showed it to be genetically distinct from N. coucang.[7]

A 2013 review of museum specimens and photographs attributed to N. menagensis resulted in elevating two of its former subspecies to the species N. bancanus and N. borneanus. Additionally, N. kayan was recognized as a new species, distinct from the nominate subspecies, N. menagensis.[8] All newly recognized or elevated species showed significant differences in their "facemask"—the coloration patterns on their face.[8] Analysis of the facemask patterns suggests that N. kayan diverged from N. menagensis and N. borneanus through sympatric speciation (divergent evolution of organisms living in the same geographic region), while geographic barriers may account for its divergence with N. bancanus (allopatric speciation).[9]

N. kayan is named after the Kayan River, which runs through its native habitat and near Peleben, the type locality of the original specimen.[10] The holotype, AMNH 106012, was originally collected on 8 October 1935 by Baron V. von Plessen near Peleben in the province of East Kalimantan in Borneo and is housed in the American Museum of Natural History in New York. It consists of a male skin and skull, with a head-body length of 257.3 mm (10.1 in).[9]

Physical description

Like other slow lorises, it has a vestigial tail, round head, and short ears.[11] It has a rhinarium (the moist, naked surface around the nostrils of the nose) and a broad, flat face with large eyes.[12] Like N. menagensis, this and all other Bornean species lack a second upper incisor, which distinguishes them from other slow lorises.[13] On its front feet, the second digit is smaller than the rest; the big toe on its hind foot opposes the other toes, which enhances its gripping power. Its second toe on the hind foot has a curved grooming claw that it uses for scratching and grooming, while the other nails are straight.[12] It also possesses a specialized arrangement of lower front teeth, called a toothcomb, which is also used for grooming, as with other lemuriform primates.[14] On the ventral side of its elbow, it has a small swelling called the brachial gland, which secretes a pungent, clear oily toxin that the animal uses defensively by wiping it on its toothcomb.[15]

The face mask of N. kayan differs from those of other Bornean lorises in several ways. First, the top of the dark ring around its eyes is either rounded or pointed (not diffuse at the edges) and the bottom stretches below the zygomatic arch, and sometimes extends as far down as the jaw. Second, the stripe between the eyes is occasionally bulb-shaped, compared to the rectangular stripe seen in the neighboring species. Also, a light band of fur in front of the ears is usually intermediate in width compared to the narrow and wide bands seen in the other Bornean species. Compared to N. menagensis, the facemask of N. kayan has more contrast between its dark black and white features, and its ears are always covered in hair, whereas those of N. menagensis are generally naked. Overall, its fur is generally longer and fluffier compared to N. menagensis.[16] Based on a limited number of specimens, the species is about 273.4 mm (10.8 in) long, and weighs about 410.5 g (0.9 lb).[10]

Distribution

N. kayan is found in central and northern Borneo. Its range extends south to the Mahakam and Rajang Rivers in the Indonesian province of East Kalimantan and the Malaysian province of Sarawak, respectively, and north to southern side of Mount Kinabalu in the Malaysian province of Sabah. Although it is not found along the coast, its range spans Borneo from east to west. Its range overlaps that of N. menagensis in East Kalimantan and Sabah,[10] and N. borneanus is a neighboring species.[16]

Habitat and ecology

Like other slow lorises, N. kayan is arboreal, nocturnal,[11] and omnivorous, eating primarily insects, tree gum, nectar, and fruit.[17] Likewise, this species has a toxic bite, a unique feature found only in slow lorises among primates. The toxin is produced by licking a brachial gland (a gland by its elbow), and the secretion mixes with its saliva to activate. The toxic bite is a deterrent to predators, and the toxin is also applied to the fur during grooming as a form of protection for infants. When threatened, slow lorises may also lick their brachial glands and bite the aggressors, delivering the toxin into the wound. Slow lorises can be reluctant to release their bite, which is likely to maximize the transfer of toxins.[18]

The face mask may help the species identify potential mates by distinguishing species, and may serve as an anti-predator strategy by making its eyes appear larger than they really are.[19]

Conservation

While Nycticebus kayan has yet to be assessed by the IUCN, N. menagensis was listed as "Vulnerable" as of 2012.[8] Because that species has been divided into four distinct species, each of the new species faces a higher risk of extinction. Accordingly, each of them are expected to be listed as "Vulnerable" at least, with some of them likely to be assigned to a higher-risk category.[20]

Between 1987 and 2012, one-third of Borneo's forests were lost, making habitat loss one of the greatest threats to the survival of N. kayan. The illegal wildlife trade is also a major factor,[8] with loris parts commonly sold for traditional medicine. Further, viral videos on YouTube promote the exotic pet trade.[20][21][22] However, all slow loris species are protected from commercial trade under Appendix I of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).[23]

References

  1. ↑ "Nycticebus kayan". Integrated Taxonomic Information System. Retrieved 28 January 2016.
  2. ↑ "Appendices I, II and III" (PDF). Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES). 2010.
  3. ↑ Munds, Nekaris & Ford 2013, p. 46.
  4. ↑ Osman Hill 1953, pp. 156–163.
  5. ↑ Groves 1971.
  6. ↑ Groves 2001, p. 99.
  7. ↑ Chen et al. 2006, p. 1198.
  8. 1 2 3 4 Munds, Nekaris & Ford 2013, p. 47.
  9. 1 2 Munds, Nekaris & Ford 2013, p. 50.
  10. 1 2 3 Munds, Nekaris & Ford 2013, p. 52.
  11. 1 2 Ankel-Simons 2007, p. 82.
  12. 1 2 Smith & Xie 2008, pp. 159–160.
  13. ↑ Munds, Nekaris & Ford 2013, p. 53.
  14. ↑ Ankel-Simons 2007, p. 246.
  15. ↑ Hagey, Fry & Fitch-Snyder 2007, p. 253.
  16. 1 2 Munds, Nekaris & Ford 2013, p. 50–52.
  17. ↑ Nekaris & Bearder 2007, pp. 28–33.
  18. ↑ Alterman 1995, pp. 421–423.
  19. ↑ Munds, Nekaris & Ford 2013, p. 49.
  20. 1 2 Wall, T. (13 December 2012). "Three new species of venomous primate identified by MU researcher". Missouri University News Bureau. Archived from the original on 24 December 2012. Retrieved 19 December 2012.
  21. ↑ Bryner, J. (14 December 2012). "Slow loris species, Nycticebus kayan, discovered in Borneo". The Huffington Post. Archived from the original on 4 January 2013. Retrieved 15 December 2012.
  22. ↑ Walker, M. (13 December 2012). "Primate species: new slow loris found in Borneo". BBC News. Archived from the original on 24 December 2012.
  23. ↑ Nekaris & Munds 2010, p. 390.

Literature cited

  • Alterman, L. (1995). "Toxins and toothcombs: potential allospecific chemical defenses in Nycticebus and Perodicticus". In Alterman, L.; Doyle, G.A.; Izard, M.K. Creatures of the Dark: The Nocturnal Prosimians. New York, New York: Plenum Press. pp. 413–424. ISBN 978-0-306-45183-6. OCLC 33441731. 
  • Ankel-Simons, F. (2007). Primate Anatomy (3rd ed.). Academic Press. ISBN 978-0-12-372576-9. 
  • Chen, J. -H.; Pan, D.; Groves, C. P.; Wang, Y. -X.; Narushima, E.; Fitch-Snyder, H.; Crow, P.; Thanh, V. N.; Ryder, O.; Zhang, H. -W.; Fu, Y.; Zhang, Y. (2006). "Molecular phylogeny of Nycticebus inferred from mitochondrial genes". International Journal of Primatology 27 (4): 1187–1200. doi:10.1007/s10764-006-9032-5. 
  • Groves, Colin P. (1971). "Systematics of the genus Nycticebus" (PDF). Proceedings of the Third International Congress of Primatology (Zürich, Switzerland) 1: 44–53. 
  • Groves, Colin P. (2001). Primate Taxonomy. Washington, DC: Smithsonian Institution Press. ISBN 978-1-56098-872-4. 
  • Hagey, L.R.; Fry, B.G.; Fitch-Snyder, H. (2007). "Talking defensively, a dual use for the brachial gland exudate of slow and pygmy lorises". In Gursky, S.L.; Nekaris, K.A.I. Primate Anti-Predator Strategies. Developments in Primatology: Progress and Prospects. Springer. pp. 253–273. doi:10.1007/978-0-387-34810-0. ISBN 978-0-387-34807-0. 
  • Munds, R. A.; Nekaris, K. A. I.; Ford, S. M. (2013) [2012 online]. "Taxonomy of the Bornean slow loris, with new species Nycticebus kayan (Primates, Lorisidae)" (PDF). American Journal of Primatology 75 (1): 46–56. doi:10.1002/ajp.22071. PMID 23255350. 
  • Nekaris, K.A.I.; Bearder, S.K. (2007). "Chapter 3: The Lorisiform Primates of Asia and Mainland Africa: Diversity Shrouded in Darkness". In Campbell, C.; Fuentes, C.A.; MacKinnon, K.; Panger, M.; Stumpf, R. Primates in Perspective. New York, New York: Oxford University Press. pp. 28–33. ISBN 978-0-19-517133-4. 
  • Nekaris, K.A.I.; Munds, R. (2010). "Chapter 22: Using facial markings to unmask diversity: the slow lorises (Primates: Lorisidae: Nycticebus spp.) of Indonesia". In Gursky-Doyen, S.; Supriatna, J. Indonesian Primates. New York: Springer. pp. 383–396. doi:10.1007/978-1-4419-1560-3_22. ISBN 978-1-4419-1559-7. 
  • Osman Hill, W.C. (1953). Primates Comparative Anatomy and Taxonomy I—Strepsirhini. Edinburgh Univ Pubs Science & Maths, No 3. Edinburgh University Press. OCLC 500576914. 
  • Smith, Andrew T.; Xie, Yan (2008). A Guide to the Mammals of China. Princeton University Press. ISBN 978-0-691-09984-2. 

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