|Scientific Name:||Viverra tangalunga|
|Species Authority:||Gray, 1832|
|Taxonomic Notes:||Veron et al. (2014) considered that the population on Belitung island (Indonesia) is so distinct genetically that it should be recognised as an evolutionarily significant unit and managed separately from all other populations of the species.|
|Red List Category & Criteria:||Least Concern ver 3.1|
|Assessor(s):||Duckworth, J.W., Mathai, J., Wilting, A., Holden, J., Hearn, A. & Ross, J.|
|Contributor(s):||Mohamed, A., Hon, J., Cheyne, S., Brodie, J., Veron, G. & Jennings, A.|
Malay Civet is listed as Least Concern because it has a relatively wide geographic distribution, is commonly recorded in much of its range, is tolerant of degraded habitats, and occurs in many protected areas; the very high camera-trapping detection rates in many studies suggest high densities and stable and large populations. Although ongoing forest loss in its range is presumably causing its population to decline, its wide occurrence outside the level lowlands and use of degraded and fragmented areas means that it is implausible that decline rates could be sufficient even for Near Threatened, either in the past or future three generations (taken as 18 years).
|Previously published Red List assessments:|
|Range Description:||Malay Civet is widespread on the large land-masses of Peninsular Malaysia, Sumatra and Borneo, in all of which it is probably native; on Sulawesi (where it is introduced) and several of the large Philippine islands (where it is evidently introduced on some, but perhaps native on others); and on many smaller islands of the Philippines, on the Sunda shelf and east to Ambon (Indonesia). Although it is evidently native (and genetically distinct) on at least Belitung, the native or introduced status on many of these smaller islands, including Singapore, is not determined, but there is no evidence of natural dispersal east of Wallace's line. Overall, human-mediated dispersal has been very important in generating today's geographic range (Jennings and Veron 2011, Lim and Ou Yang 2012, Veron et al. 2014). There are several records from Java, but there is no evidence of a native population there (Jennings and Veron 2011); a small level of (presumably imported) trade continues there (Nijman et al. 2014). In the Philippines, it has been recorded on Bohol, Busuanga, Camiguin, Catanduanes, Culion, Guimaras, Leyte, Lubang, Luzon, Mindanao, Mindoro, Negros, Palawan, Panay, Samar, Sibuyan and Siquijor (Timm and Birney 1980, Heaney and Tabaranza 1991, Heaney et al. 1991, Jennings and Veron 2011). In Malaysia, it is found in Borneo, Banggi Island, Langkawi Island, Penang Island and on mainland Peninsular Malaysia (Corbet and Hill 1992, Nor 1996, Meiri 2005). In Indonesia, it has been recorded on Ambon, Bacan, Bangka, Bauwal, Belitung, Bintan, Borneo, Bunguran, Buru, Halmahera, Karimata, Kundur, Laut, Lingga, Natuna, Panebangan, Rupat, Sangihe, Seram, Siao, Sumatra, Ternate, and Watubela (Jennings and Veron 2011). Wozencraft (2005) listed it, in addition to its known range, for Cambodia and Thailand, and it was mapped for the southern portion of the latter by Veron et al. (2014); but there is no evidence that it occurs in either of these countries (Holden and Neang 2009, Chutipong et al. 2014). It is perhaps more localised on Sumatra than on Borneo, occurring mainly in the east: J. Holden (pers. comm. 2014) knows of no recent records from the west, and Jennings and Veron (2011) traced only three records ever from this part of the island.|
It has been recorded from sea-level to 2,100 m (Jennings and Veron 2011).
Native:Indonesia (Kalimantan, Maluku - Introduced, Sulawesi - Introduced, Sumatera); Malaysia (Peninsular Malaysia, Sabah, Sarawak)
Present - origin uncertain:Philippines; Singapore
|Range Map:||Click here to open the map viewer and explore range.|
|Population:||Malay Civet is often amongst the most commonly recorded small carnivores in camera-trap and other surveys on Borneo, including those in old-growth forest (e.g., Belden et al. 2007, Cheyne et al. 2010, Mathai et al. 2010, Wilting et al. 2010, Brodie and Giordano 2011, Samejima and Semiadi 2012). It also seems to be common in West Malaysia (e.g., Low 2011). By contrast, some high-effort surveys - including several focused on old-growth forest - in Sumatra (e.g., Holden 2006, McCarthy and Fuller 2014, G. Fredriksson pers. comm. 2014, J. Holden pers. comm. 2014) have failed to find it at all. Without a clearer understanding of habitat use - which perhaps varies between land-mass - it is difficult to make firm statements about population trends. Whilst it evidently remains widespread and common in Borneo, there is insufficient information to be sure that this applies also to the other large landmasses to which it is native, peninsular Malaysia and Sumatra.|
|Current Population Trend:||Stable|
|Habitat and Ecology:||Malay Civet occurs in a variety of habitats including primary and secondary forests, cultivated land and the outskirts of villages (Wemmer and Watling 1986, Colon 2002, Azlan 2003, Jennings et al. 2006, Jennings and Veron 2011). It is widely and readily camera-trapped in old-growth forest on Borneo (e.g. Belden et al. 2007, Cheyne et al. 2010, Mathai et al. 2010, Wilting et al. 2010, Brodie and Giordano 2011, Samejima and Semiadi 2012). By contrast, the number of reasonably intensive surveys that have not found it in superficially similar habitat on Sumatra suggests some patchiness of occurrence on that island: such surveys include Holden (2006), McCarthy and Fuller (2014), WCS Indonesia (pers. comm. 2008; many thousand camera-trap nights in Bukit Barisan Selatan National Park) and G. Fredriksson (pers. comm. 2014; about 10,000 camera-trap nights in Batang Toru); Holden (2006) had, however, some incidental records from degraded areas outside the camera-trapped old-growth forest of Kerinci Seblat. Similarly, it was recorded in a camera-trap survey of two lowland oil palm plantations in central Sumatra far from extensive old-growth forest; although records were strongly clustered around the plantation edge, indicating a need for microhabitats (perhaps dense undergrowth, fallen wood) absent from the plantations proper (Jennings et al. 2015); another oil palm plantation-focussed survey in central Sumatra found it commonly in the landscape but did not record it in the plantation itself (Maddox et al. 2007). |
In one area of Borneo, Malay Civet density in an unlogged forest was about twice that in a logged forest, perhaps because of lower fruit availability in logged forest; potentially, the species might survive in disturbed habitats only by continued inward dispersal from un- or little-disturbed forest (Colon 2002). Also in Malaysian Borneo, J. Brodie (pers. comm. 2014) found that local conservation status was affected negatively by recent logging, but had recovered somewhat in forests that were logged more than 10 years previously. In Sabah, Malaysia, the Proportion of Area Occupied seemed generally higher in less degraded than in more degraded forests, but other factors (as yet unclear) made this far from a perfect link (Sollmann et al. in prep.). In Peninsular Malaysia, radio-tracking of seven Malay Civets in an area of lowland forest abutting plantations found them to use both habitats, concluding that forest was essential, that the civets merely ranged into plantations perhaps primarily for nocturnal feeding, and that suitable day-bed sites might be limiting in them (Jennings et al. 2010), a pattern echoed in Sumatra (Jennings et al. 2015). Similarly, on Borneo, Malay Civet was commonly found within oil palm plantations near the Danum Valley Conservation Area (J. Brodie pers. comm. 2014) and the Sepilok Forest Reserve (A. Hearn pers. comm 2015), mostly fairly close to (within 2 km of; but so were most camera-trap stations) forest or mangrove. These findings suggest that the use by Malay Civet of converted areas - a least of oil palm - may be less than is often assumed.
It has been recorded from sea-level to 2,100 m (Jennings & Veron 2011) but the latter is perhaps exceptionally high; in Borneo, the highest record traced by Payne et al. (1985) was only 1,100 m; subsequent records go up only to 1,452 m (Crocker Range), although this was also the upper limit of camera-trapping, so it might occur still higher (J. Ross and A. Hearn pers. comm. 2014). In an area of Sarawak with significant highland survey, Mathai et al. (2010) speculated that this species might occur mostly below 900 m. The highest record in the Philippines given by Rabor (1955), Rickart et al. (1993) or Heaney et al. (in press) was only 1,200 m.
Malay Civet is solitary, omnivorous and primarily ground-dwelling (Kanchanasakha et al. 1998). Documented home-range sizes include, on Sulawesi, 24–189 ha, and on Borneo, 27–283 ha (Macdonald and Wise 1979, Nozaki et al. 1994, Colon 2002, Jennings et al. 2006). Mean home-range size for adults of both sexes was 110 ha in Sabah and 70 ha on Sulawesi (Colon 2002, Jennings et al. 2006). Colon (2002) considered that the Malay Civet was not territorial in Sabah but Jennings et al. (2006) found low intra-sexual overlap on Buton Island. Malay Civet is mainly nocturnal, although more active during daylight on Buton Island, Sulawesi than in Sabah, East Malaysia (Colon 2002, Azlan 2005, Jennings et al. 2006). Day rest sites are typically situated at ground level and associated with some form of cover (Colon 2002, Jennings et al. 2006).
|Generation Length (years):||5.9|
|Movement patterns:||Not a Migrant|
|Use and Trade:||Malay Civet is perhaps not specifically sought quarry anywhere in its range, but because much hunting uses non-selective traps, it is part of the general catch of wildlife (e.g. Mathai et al. 2010). The extensive introduction of the species in previous centuries outside its native range (Veron et al. in press) indicates it was presumably formerly perceived as of value.|
|Major Threat(s):||As a ground-living species, Malay Civet is exposed to snaring and other forms of ground-level trapping, to hunting with dogs, and to death from feral/stray dogs (e.g. Mathai et al. 2010, Azhar et al. 2013). Leopard Cats Prionailurus bengalensis in oil palm plantations die from haemorrhaging through eating rats poisoned by Warfarin and other anti-coagulant baits (Duckett 1976), and these would presumably affect other mammalian predators such as this civet, if it uses such plantations heavily. However, the limited survey in areas heavily used by people suggests it is rather well able to persist in landscapes retaining some patches of native forest, at general levels of threat. The species is occasionally hunted for food and treated as a pest because it is perceived as raiding poultry. In recent centuries and particularly recent decades, much of its range has been deforested. While the species is frequently recorded in edge and degraded areas, there is no indication that it can survive in non-wooded landscapes, or that oil palm plantations (which have replaced forest in much of its range) can support populations in the absence of forest. Forest conversion rates have considerably slowed in some of its range (e.g. Sabah, Malaysia) but remain high in some other parts (e.g. Sumatra); throughout, the highest losses tend to be in the level lowlands, which comprise part of the core habitat of this species.|
|Conservation Actions:||Malay Civet is found in many protected areas across its range. This species is partly protected in Malaysia under the Wildlife Protection Act of 1972, meaning that anyone found killing this species will be liable to a fine not exceeding three thousand ringgit (Approx. USD 790) or a term of imprisonment not exceeding three years, or both (Azlan, 2003). However, Section 55 of this Act allows farmers to shoot any wild animal that causes damage to their property, as long as reasonable efforts have been made to frighten the animal away, and many civets are considered as pests in Peninsular Malaysia, because they are perceived to prey on small livestock and raid fruit orchards (Azlan 2003). It is not a Totally Protected Species in Indonesia (Shepherd 2008) and neither is it a CITES listed species (CITES 2014). The wide persistence in encroached areas in close proximity to people indicates a lack of immediate conservation measures needed; and while the habitat use remains poorly clarified, there is no evidence that this lack of knowledge is placing the species at risk through obscuring the need for interventions.|
|Citation:||Duckworth, J.W., Mathai, J., Wilting, A., Holden, J., Hearn, A. & Ross, J. 2016. Viverra tangalunga. The IUCN Red List of Threatened Species 2016: e.T41708A45220284.Downloaded on 27 February 2017.|
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