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Asian palm civet

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Asian palm civet
Asian palm civet in Khao Yai National Park, Thailand
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Carnivora
Suborder: Feliformia
Family: Viverridae
Genus: Paradoxurus
Species:
P. hermaphroditus[1]
Binomial name
Paradoxurus hermaphroditus[1]
(Pallas, 1777)
Asian palm civet range: native in green, introduced in red

The Asian palm civet (Paradoxurus hermaphroditus), also called common palm civet, toddy cat and musang, is a viverrid native to South and Southeast Asia. Since 2008, it is IUCN Red Listed as Least Concern as it accommodates to a broad range of habitats. It is widely distributed with large populations that in 2008 were thought unlikely to be declining. It is threatened by poaching for the illegal wildlife trade.

Characteristics

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Close up of an Asian palm civet
Illustration of skull and dentition, by Gervais in Histoire naturelle des mammifères

The Asian palm civet's long, stocky body is covered with coarse, shaggy hair that is usually greyish in colour. It has a white mask across the forehead, a small white patch under each eye, a white spot on each side of the nostrils, and a narrow dark line between the eyes. The muzzle, ears, lower legs, and distal half of the tail are black, with three rows of black markings on the body. Its head-to-body length is about 53 cm (21 in) with a 48 cm (19 in) long unringed tail. It weighs 2 to 5 kg (4.4 to 11.0 lb). Its anal scent glands emit a nauseating secretion as a chemical defense when threatened or upset.[3]

Distribution and habitat

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The Asian palm civet is widely distributed in South and Southeast Asia, ranging from India, Nepal, Bangladesh, Bhutan, Myanmar, Sri Lanka to Thailand, Singapore, Peninsular Malaysia, Sabah, Sarawak, Brunei Darussalam, Laos, Cambodia, Vietnam, China, the Philippines and the Indonesian islands of Sumatra, Java, Kalimantan, Bawean and Siberut.[2] It usually inhabits primary forests, but also occurs at lower densities in secondary and selectively logged forest.[4]

It was introduced to Irian Jaya, the Lesser Sunda Islands, Maluku, and Sulawesi. Its presence in Papua New Guinea is uncertain.[2]

Behaviour and ecology

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Asian palm civet on a tree at Kerala, India
Asian palm civet with pups in an urban area at Baranagar, Kolkata, India

The Asian palm civet is thought to lead a solitary lifestyle, except for brief periods during mating. It is both terrestrial and arboreal, showing a nocturnal activity pattern with peaks between late evening until after midnight.[4] It is usually active between dawn and 4:00 in the morning, but less active during nights when the moon is brightest.[5]

Scent marking behaviour and olfactory response to various excretions such as urine, feces, and secretion of the perineal gland differs in males and females. Scent marking by dragging the perineal gland and leaving the secretion on the substrate was most commonly observed in animals of both sexes. The duration of the olfactory response varied and depended both on the sex and excretion type. The palm civet can distinguish animal species, sex, familiar and unfamiliar individuals by the odor of the perineal gland secretion.[6]

Feeding and diet

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The Asian palm civet is an omnivore feeding foremost on fruits such as berries and pulpy fruits. It thus helps to maintain tropical forest ecosystems via seed dispersal.[4] It eats chiku, mango and rambutan, but also small mammals and insects. It plays an important role in the natural regeneration of Pinanga kuhlii and P. zavana palms at Gunung Gede Pangrango National Park.[7]

Reproduction

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Juvenile Asian palm civet

Due to its solitary and nocturnal habits, little is known about its reproductive processes and behaviour.[8] In March 2010, a pair of palm civets was observed when attempting to mate. The pair copulated on the tree branch for about five minutes. During that period, the male mounted the female 4–5 times. After each mounting, the pair separated for a few moments and repeated the same procedure. After completion of mating, the pair frolicked around for some time, moving from branch to branch on the tree. The animals separated after about six minutes and moved off to different branches and rested there.[9]

Threats

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Asian palm civet housed in a cage for the production of kopi luwak

Since 2008, the Asian palm civet is IUCN Red Listed as Least Concern. The global population was thought to be large and unlikely to be declining as of 2008. It is threatened by hunting and trapping, in particular in southern China; in some parts of India, some ethnic tribes kill and consume its meat.[2] The oil extracted from small pieces of the meat, kept in linseed oil in a closed earthen pot and regularly sunned, is used indigenously as a cure for scabies.[10]

In Indonesia, it is threatened by poaching and the illegal wildlife trade; buyers use it for the production of kopi luwak made from coffee beans digested and excreted by Asian palm civets.[11] They are housed in battery cage systems, which have been criticised on animal welfare grounds.[12][13]

In some parts of its range, Asian palm civets are hunted for bushmeat and the pet trade.[14]

Conservation

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The Asian palm civet is listed on CITES Appendix III.[2] There is a quota in place in Indonesia, precluding trade from certain areas, setting a cap on the number of civets that can be taken from the wild, and allowing only 10% of those removed from the wild to be sold domestically. This quota is largely ignored by hunters and traders and is not enforced by authorities.[15] This species has become popular as a pet in Indonesia in recent years, causing a rise in the numbers found in markets in Java and Bali. The majority of the animals sold as pets originate from the wild. The high numbers of animals seen, lack of adherence to the quota and lack of enforcement of the laws are causes for conservation concern.[14]

Taxonomy and evolution

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Illustrations of Asian palm civets in Pocock's The fauna of British India, including Ceylon and Burma. Mammalia. – Volume 1[16]
Philippine palm civet

Viverra hermaphrodita was the scientific name proposed by Peter Simon Pallas in 1777.[17] It is the nominate subspecies and ranges in Sri Lanka and southern India as far north as the Narbada River.[16] Several zoological specimens were described between 1820 and 1992:[1]

  • Viverra bondar by Anselme Gaëtan Desmarest in 1820 was a specimen from Bengal[18]
  • Viverra musanga by Stamford Raffles in 1821 was a specimen from Sumatra[19]
  • Viverra musanga, var. javanica by Thomas Horsfield in 1824 was a specimen from Java[20]
  • Paradoxurus pallasii by John Edward Gray in 1832 was a specimen from India[21]
  • Paradoxurus philippinensis by Claude Jourdan in 1837 was a specimen from the Philippines[22] However, a genetic study in 2015 reclassifies it as a separate species.[23]
  • P. h. setosus by Honoré Jacquinot and Pucheran in 1853
  • P. h. nictitans by Taylor in 1891 was a specimen from Odisha;[16]
  • P. h. lignicolor by Gerrit Smith Miller Jr. in 1903
  • P. h. minor by John Lewis Bonhote in 1903
  • P. h. canescens by Lyon in 1907
  • P. h. milleri by Cecil Boden Kloss in 1908
  • P. h. kangeanus by Oldfield Thomas in 1910
  • P. h. sumbanus by Ernst Schwarz in 1910
  • P. h. exitus by Schwarz in 1911
  • P. h. cochinensis by Schwarz, 1911
  • P. h. canus (Miller, 1913)
  • P. h. pallens (Miller, 1913)
  • P. h. parvus (Miller, 1913)
  • P. h. pugnax (Miller, 1913)
  • P. h. pulcher (Miller, 1913)
  • P. h. sacer (Miller, 1913)
  • P. h. senex (Miller, 1913)
  • P. h. simplex (Miller, 1913)
  • P. h. enganus by Lyon, 1916
  • P. h. laotum by Nils Carl Gustaf Fersen Gyldenstolpe in 1917 was a specimen from Chieng Hai in north-western Thailand, and ranges from Myanmar to Indochina and Hainan;[16]
  • P. h. balicus by Sody in 1933 was a specimen from Bali
  • P. h. scindiae by Pocock in 1934 was a specimen from Gwalior, and ranges in central India;[16]
  • P. h. vellerosus by Pocock in 1934 was a specimen from Kashmir;[16]
  • P. h. dongfangensis by Corbet and Hill in 1992

The taxonomic status of these subspecies has not yet been evaluated.[2]

Evolution

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Palawan and Borneo specimens are genetically close, so the Asian palm civet on Palawan island might have dispersed from Borneo during the Pleistocene. It is possible that people later introduced Asian palm civet into other Philippines islands.[24][25]

In culture

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In Philippine mythology, the Bagobo people believe a being named Lakivot was said to be a huge and powerful palm civet who can talk. Lakivot defeated various monsters, including the one-eyed monster Ogassi and the busaw beings who guarded the Tree of Gold, which had the Flower of Gold that he sought. He was eventually transformed into a handsome young man, and married the person to whom he gave the Flower of Gold.[26] The Philippine twenty-peso note currently features the Asian palm civet on the reverse side.[27]

References

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  1. ^ a b Wozencraft, W. C. (2005). "Species Paradoxurus hermaphroditus". In Wilson, D. E.; Reeder, D. M. (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. pp. 532–628. ISBN 978-0-8018-8221-0. OCLC 62265494.
  2. ^ a b c d e f Duckworth, J.W.; Timmins, R.J.; Choudhury, A.; Chutipong, W.; Willcox, D.H.A.; Mudappa, D.; Rahman, H.; Widmann, P.; Wilting, A. & Xu, W. (2016). "Paradoxurus hermaphroditus". IUCN Red List of Threatened Species. 2016: e.T41693A45217835. doi:10.2305/IUCN.UK.2016-1.RLTS.T41693A45217835.en. Retrieved 19 November 2021.
  3. ^ Lēkhakun, B.; McNeely, J. A. (1977). Mammals of Thailand. Bangkok: Association for the Conservation of Wildlife.
  4. ^ a b c Grassman, L.I. Jr. (1998). "Movements and fruit selection of two Paradoxurinae species in a dry evergreen forest in Southern Thailand". Small Carnivore Conservation (19): 25–29.
  5. ^ Joshi, A.R.; Smith, J.L.D.; Cuthbert, F.J. (1995). "Influence of food distribution and predation pressure on spacing behavior in palm civets". Journal of Mammalogy. 76 (4). American Society of Mammalogists: 1205–1212. doi:10.2307/1382613. JSTOR 1382613.
  6. ^ Rozhnov, V. V.; Rozhnov, Y. V. (2003). "Roles of Different Types of Excretions in Mediated Communication by Scent Marks of the Common Palm Civet, Paradoxurus hermaphroditus Pallas, 1777 (Mammalia, Carnivora)". Biology Bulletin. 30 (6). MAIK Nauka/Interperiodica: 584–590. Bibcode:2003BioBu..30..584R. doi:10.1023/B:BIBU.0000007715.24555.ed. S2CID 19102865.
  7. ^ Thohari, M.; Santosa, Y. (1986). A preliminary study on the role of civet (Paradoxurus hermaphroditus) in the natural regeneration of palms (Pinanga kuhlii and P. zavana) at Gunung Gede-Pangrango National Park, West Java (Indonesia). Symposium on Forest Regeneration in Southeast Asia, 9–11 May 1984. Biotrop Special Publication. pp. 151–153.
  8. ^ Prater, S. H. (1980). The book of Indian animals (Second ed.). Bombay, India: Bombay Natural History Society.
  9. ^ Borah, J.; Deka, K. (2011). "An observation of Common Palm Civet Paradoxurus hermaphroditus mating". Small Carnivore Conservation. 44: 32–33.
  10. ^ Singh, L.A.K. (1982). "Stomach contents of a common palm civet, Paradoxurus hermaphroditus (Pallas)". Journal of the Bombay Natural History Society. 79 (2): 403–404.
  11. ^ Shepherd, C. (2012). "Observations of small carnivores in Jakarta wildlife markets, Indonesia, with notes on trade in Javan Ferret Badger Melogale orientalis and on the increasing demand for Common Palm Civet Paradoxurus hermaphroditus for civet coffee production". Small Carnivore Conservation. 47: 38–41.
  12. ^ Penha, J. (2012). "Excreted by imprisoned Civets, Kopi Luwak no longer a personal favorite". The Jakarta Globe. Archived from the original on 16 January 2013. Retrieved 17 August 2012.
  13. ^ Milman, O. (2012). "World's most expensive coffee tainted by 'horrific' civet abuse". The Guardian. London. Archived from the original on 4 June 2017. Retrieved 25 November 2012.
  14. ^ a b Nijman, V.; Spaan, D.; Rode-Margono, E. J.; Roberts, P. D.; Wirdateti; Nekaris, K. A. I. (2014). "Trade in common palm civet Paradoxurus hermaphroditus in Javan and Balinese markets, Indonesia". Small Carnivore Conservation (51): 11−17.
  15. ^ Shepherd, C. R. (2008). "Civets in trade in Medan, North Sumatra, Indonesia (1997–2001) with notes on legal protection" (PDF). Small Carnivore Conservation. 38: 34–36. Archived January 29, 2015, at the Wayback Machine
  16. ^ a b c d e f Pocock, R. I. (1939). "Paradoxurus hermaphroditus". The Fauna of British India, including Ceylon and Burma. Vol. 1. Mammalia. London: Taylor and Francis. pp. 387–415.
  17. ^ Pallas, P. S. (1778). "Das Zwitterstinkthier". In Schreber, J. C. D. (ed.). Die Säugethiere in Abbildungen nach der Natur, mit Beschreibungen. Erlangen: Wolfgang Walther. p. 426.
  18. ^ Desmarest, A.G. (1820). "Civette Bondar". Mammalogie, ou, Description des espèces de mammifères. Vol. Premiere Partie. Paris: Chez Mme. Veuve Agasse. p. 210.
  19. ^ Raffles, S. (1821). "Descriptive Catalogue of a Zoological Collection, made on account of the Honourable East India Company, in the Island of Sumatra and its Vicinity, under the Direction of Sir Thomas Stamford Raffles, Lieutenant-Governor of Tort Marlborough; with additional Notices illustrative of the Natural History of those Countries". Transactions of the Linnean Society of London. 13: 239–275.
  20. ^ Horsfield, T. (1824). "Viverra musanga, var. javanica". Zoological researches in Java, and the neighbouring islands. London: Kingsbury, Parbury & Allen. pp. 148–151.
  21. ^ Gray, J.E. (1832). "Pallas's Paradoxurus". Illustrations of Indian zoology; chiefly selected from the collection of Major-General Hardwicke. London: Treuttel, Wurtz, Treuttel, Jun. and Richter. pp. Plate 8.
  22. ^ Jourdan, C. (1837). "Mémoire sur quelques mammifères nouveaux". Comptes Rendus de l'Académie des Sciences. 5 (15): 521–524. Archived from the original on 2021-02-08. Retrieved 2020-05-27.
  23. ^ Veron, Géraldine; Patou, Marie-Lilith; Tóth, Mária; Goonatilake, Manori; Jennings, Andrew P. (2015). "How many species of Paradoxurus civets are there? New insights from India and Sri Lanka". Journal of Zoological Systematics and Evolutionary Research. 53 (2): 161–174. doi:10.1111/jzs.12085.
  24. ^ Patou, M.L.; Wilting, A.; Gaubert, P.; Esselstyn, J.A.; Cruaud, C.; Jennings, A.P.; Fickel, J. & Veron, G. (2010). "Evolutionary history of the Paradoxurus palm civets – a new model for Asian biogeography". Journal of Biogeography. 37 (11): 2092–2093. Bibcode:2010JBiog..37.2077P. doi:10.1111/j.1365-2699.2010.02364.x. S2CID 2705179.
  25. ^ Piper, P.J.; Ochoa, J.; Robles, E.C.; Lewis, H. & Paz, V. (2011). "Palaeozoology of Palawan Island, Philippines". Quaternary International. 233 (2): 142−158. Bibcode:2011QuInt.233..142P. doi:10.1016/j.quaint.2010.07.009.
  26. ^ Esteban, R.C. (2011). Folktales of Southern Philippines. Manila: Anvil Publishers.
  27. ^ Plata, M.J. (2020). "The Different Animals Featured On Philippine Peso Bills". flipscience. Retrieved May 20, 2024.
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