Asian palm civet

Last updated

Asian palm civet
Common Palm Civet (Paradoxurus hermaphroditus) (7781509830).jpg
Asian palm civet in Khao Yai National Park, Thailand
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Carnivora
Suborder: Feliformia
Family: Viverridae
Genus: Paradoxurus
Species:
P. hermaphroditus [2]
Binomial name
Paradoxurus hermaphroditus [2]
(Pallas, 1777)
Asian Palm Civet area.png
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.

Contents

Characteristics

Close up of an Asian palm civet Himalay Palm Civet.jpg
Close up of an Asian palm civet
Illustration of skull and dentition, by Gervais in Histoire naturelle des mammiferes Paradoxureskull.png
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

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. [1] 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. [1]

Behaviour and ecology

Asian palm civet on a tree at Kerala, India Asian Palm Civet Over A Tree.jpg
Asian palm civet on a tree at Kerala, India
Asian palm civet with pups in an urban area at Baranagar, Kolkata, India Asian Palm Civet with pups Baranagar Kolkata West Bengal India.jpg
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

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

Juvenile Asian palm civet Paradox hermaph 060924 ltn.jpg
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

Asian palm civet housed in a cage for the production of kopi luwak Luwak (civet cat) in cage.jpg
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. [1] 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

The Asian palm civet is listed on CITES Appendix III. [1] 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

Illustrations of Asian palm civets in Pocock's The fauna of British India, including Ceylon and Burma. Mammalia. - Volume 1 Asianpalmcivetheads.png
Illustrations of Asian palm civets in Pocock's The fauna of British India, including Ceylon and Burma. Mammalia. – Volume 1
Philippine palm civet ParadoxurusHermaphroditusPhilippinensis01.jpg
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: [2]

The taxonomic status of these subspecies has not yet been evaluated. [1]

Evolution

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

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]

Related Research Articles

<span class="mw-page-title-main">Viverridae</span> Family of carnivorans

Viverridae is a family of small to medium-sized, feliform mammals. The viverrids comprise 33 species placed in 14 genera. This family was named and first described by John Edward Gray in 1821. Viverrids occur all over Africa, southern Europe, and South and Southeast Asia, across the Wallace Line.

<span class="mw-page-title-main">African palm civet</span> Species of carnivore

The African palm civet, also known as the two-spotted palm civet, is a small feliform mammal widely distributed in sub-Saharan Africa. It is listed as least concern on the IUCN Red List.

<span class="mw-page-title-main">African civet</span> Species of carnivore

The African civet is a large viverrid native to sub-Saharan Africa, where it is considered common and widely distributed in woodlands and secondary forests. It is listed as Least Concern on the IUCN Red List since 2008. In some countries, it is threatened by hunting, and wild-caught individuals are kept for producing civetone for the perfume industry.

<span class="mw-page-title-main">Malabar large-spotted civet</span> Species of carnivore

The Malabar large-spotted civet, also known as the Malabar civet, is a viverrid endemic to the Western Ghats of India. It is listed as Critically Endangered on the IUCN Red List as the population is estimated to number fewer than 250 mature individuals. It has not been recorded during surveys carried out between 1990 and 2014. In the early 1990s, isolated populations still survived in less disturbed areas of South Malabar but were seriously threatened by habitat destruction and hunting outside protected areas.

<i>Paradoxurus</i> Genus of carnivores

Paradoxurus is a genus of three palm civets within the viverrid family that was denominated and first described by Frédéric Cuvier in 1822. The Paradoxurus species have a broad head, a narrow muzzle with a large rhinarium that is deeply sulcate in the middle. Their large ears are rounded at the tip. The tail is nearly as long as the head and body.

<span class="mw-page-title-main">Sulawesi palm civet</span> Species of carnivore

The Sulawesi palm civet, also known as Sulawesi civet, musang and brown palm civet is a little-known viverrid endemic to Sulawesi. It is listed as Vulnerable on the IUCN Red List due to population decline estimated to have been more than 30% over the last three generations inferred from habitat destruction and degradation.

<span class="mw-page-title-main">Small Indian civet</span> Species of mammal

The small Indian civet is a civet native to South and Southeast Asia. It is listed as Least Concern on the IUCN Red List because of its widespread distribution, widespread habitat use and healthy populations living in agricultural and secondary landscapes of many range states.

<span class="mw-page-title-main">Banded palm civet</span> Species of carnivore

The banded palm civet, also called the banded civet, is a viverrid native to Indomalaya. They primarily inhabit lowland conifer habitat, which is under threat from encroaching human activity. It is estimated the population of the banded palm civet has decreased by around 30% in just three generations. Banded palm civets are usually approximately the size of a domestic cat; their fur is pale but with dark bands on the back. They are believed to be closely related to Hose's palm civets, which are similar in appearance and distribution.

<span class="mw-page-title-main">Small-toothed palm civet</span> Species of carnivore

The small-toothed palm civet, also known as the three-striped palm civet, is a viverrid native to dense forests of Southeast Asia, from the Assam district of India to Indochina and the Malay Peninsula and on Sumatra, Bangka, Java, Borneo, and numerous small nearby islands of Indonesia.

<span class="mw-page-title-main">Golden palm civet</span> Species of carnivore

The golden palm civet is a viverrid endemic to Sri Lanka. It is listed as Vulnerable on the IUCN Red List. Its distribution is severely fragmented, and the extent and quality of its habitat in Sri Lanka's hill regions are declining.

<span class="mw-page-title-main">Brown palm civet</span> Species of carnivore

The brown palm civet, also called the Jerdon's palm civet, is a viverrid endemic to the Western Ghats of India.

<span class="mw-page-title-main">Malayan civet</span> Species of carnivore

The Malayan civet, also known as the Malay civet and Oriental civet, is a viverrid native to the Malay Peninsula and the islands of Sumatra, Bangka, Borneo, the Riau Archipelago, and the Philippines. It is listed as "Least Concern" by IUCN as it is a relatively widely distributed, appears to be tolerant of degraded habitats, and occurs in a number of protected areas.

<span class="mw-page-title-main">Civet</span> Mammals of the families Viverridae and Nandiniidae and the genus Fossa

A civet is a small, lean, mostly nocturnal mammal native to tropical Asia and Africa, especially the tropical forests. The term civet applies to over a dozen different species, mostly from the family Viverridae. Most of the species's diversity is found in southeast Asia. Civets do not form a monophyletic group, as they consist only of certain members of the Viverridae, Eupleridae, and Nandiniidae.

<span class="mw-page-title-main">Paradoxurinae</span> Subfamily of carnivores

Paradoxurinae is a subfamily of the feliform viverrids that was denominated and first described by John Edward Gray in 1864. Pocock subordinated the genera Paradoxurus, Paguma and Arctictis to this subfamily.

<span class="mw-page-title-main">Binturong</span> Asian mammal also known as a bearcat

The binturong, also known as the bearcat, is a viverrid native to South and Southeast Asia. It is uncommon in much of its range, and has been assessed as Vulnerable on the IUCN Red List because of a declining population. It is estimated to have declined at least 30% since the mid-1980s. The binturong is the only species in the genus Arctictis.

<span class="mw-page-title-main">Hukaung Valley Wildlife Sanctuary</span> Wildlife sanctuary in northern Myanmar

Hukaung Valley Wildlife Sanctuary is a protected area in northern Myanmar, covering 17,373.57 km2 (6,707.97 sq mi). It was established in 2004 and extended to its present size in 2010. It was initially gazetted in 2004 with an area of 6,371 km2 (2,460 sq mi) in Tanaing Township and extended to Kamaing, Nayun and Kamti Townships. In elevation, it ranges from 125 to 3,435 m in the Hukawng Valley located in Kachin State and Sagaing Region. It harbours evergreen and mixed deciduous forests.

Htamanthi Wildlife Sanctuary is a 2,150.73 km2 (830.40 sq mi) large protected area in northern Myanmar. It was established in 1974 in the Sagaing Region.

<span class="mw-page-title-main">Tanintharyi Nature Reserve</span>

Tanintharyi Nature Reserve is a strict nature reserve in Myanmar's Tenasserim Hills, covering 1,699.99 km2 (656.37 sq mi). In elevation, it ranges from at an elevation of 20–130 m (66–427 ft). Most of the tropical rain forest is evergreen, interspersed with some grassland. The reserve provides habitat to Asian elephant and Gurney's pitta. It was gazetted in 2005 for the maintenance of natural resources, scientific research and education of local people in surrounding communities.

References

  1. 1 2 3 4 5 6 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.
  2. 1 2 3 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.
  3. Lēkhakun, B.; McNeely, J. A. (1977). Mammals of Thailand. Bangkok: Association for the Conservation of Wildlife.
  4. 1 2 3 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. 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. 1 2 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. 1 2 3 4 5 6 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. 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.