Overview

Distribution

Range Description

This species is only known from the provinces of Banten, West Java, and at least as far east as the western part of East Java in Indonesia.
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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
This species is nocturnal and arboreal, and is found in secondary disturbed forest, in plantations and to some extent in primary forests. It needs arboreal connectivity (vines and lianas) due to its unique locomotor adaptations, although it can cross short open spaces on the ground. It feeds on sap and floral florescence and gum but also on fruit and insects (Moore 2012; Wirdateti et al. 2004, 2011; A. Nekaris et al. unpublished data). The species sleeps alone, but more commonly in units of two or three individuals and in groups of up to six, in vegetation ranging from 2-30 m. It is often found in dense bamboo or branch tangles but not in tree holes (Wirdateti et al. 2004; A. Nekaris et al. unpublished data). Home ranges vary with habitat, ranging from 3-30 ha. Although often seen alone, social pairs and trios can occur, as can adult infant/juvenile pairs. Occurs from sea level to 1,600 m, although it is less common at higher elevations.

Systems
  • Terrestrial
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Conservation

Conservation Status

IUCN Red List Assessment


Red List Category
CR
Critically Endangered

Red List Criteria
A2cd+4cd

Version
3.1

Year Assessed
2013

Assessor/s
Nekaris, K.A.I. , Shekelle, M, Wirdateti, Rode, E.J. & Nijman, V.

Reviewer/s
Schwitzer, C.

Contributor/s

Justification
This species is listed as Critically Endangered based on a combination of historic forest loss and continued degradation meaning that less than 20% of habitat suitable for N. javanicus remains. Species distribution modelling and a gap analysis have also revealed that the remaining subpopulations of N. javanicus are highly fragmented, with only 17% of the potential distribution within the protected area network (Thorn et al. 2009). Adding to this, the species has experienced a suspected decline of at least 80% over the last 24 years (equals three generations; Nadler et al . 2007) due to severe and persistent and ongoing persecution for the pet trade (Nekaris et al. 2010).

History
  • 2008
    Endangered
  • 2000
    Data Deficient
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Population

Population
This species has been recorded at very low densities (0.02-0.20/km) (Nekaris et al. 2008). Several surveys in large forest blocks revealed few or no slow loris (Ujung Kulon, Halimun-Salak, Gede Pangrango, Masigit Kareumbi, Slamet, Dieng). Some small isolated populations persist in gardens and agricultural lands where they are at high risk from hunting and easily poached for the pet trade; severe population declines in these habitats have been documented (Wirdateti et al. 2004, 2011).

Population Trend
Decreasing
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Threats

Major Threats

Java is one of the world’s most densely populated areas and has a long history of deforestation. Extensive habitat loss and fragmentation threaten the Javan Slow Loris throughout its range. In comparison to other Indonesian slow lorises, N. javanicus is significantly more vulnerable to anthropogenic activity due to intensive land use by humans (Thorn et al. 2009). Lack of connectivity between protected areas also poses a threat to loris populations, with every forest area containing slow lorises being effectively isolated by several km of intensely modified and unsuitable habitat. The conversion of land to agriculural plantations is correlated with a sharp decline in slow loris population over the last 10 years (Wirdateti and Dahrudin 2011).

This species, like other slow lorises in Indonesia, is caught for use in the pet trade and to a lesser extent for traditional beliefs and folk medicines (Nekaris et al. 2010, Shepherd et al. 2004). Together with other loris species, N. javanicus is one of the most common protected primates found in animal markets in Java (Nekaris et al. 2008, Thorn et al. 2009). Due to their non-saltatory locomotion, their choice of sleeping sites in trees and bamboo that can be cut through and accessed, and nocturnal habits, the animals are easily caught by humans (Nekaris and Bearder 2011). The majority of the trade is to satisfy a large domestic demand, with a smaller proportion being smuggled abroad to destinations like the Middle East and Japan. The trade chain poses a perilous threat for many reasons. Conditions during transport (stuffed in boxes or sacks) and inappropriate husbandry techniques (poor diet and social housing, forced diurnal activity, excessive handling) afterwards result in large mortality rate. Slow lorises are the only venomous primates; to avoid their bites middle men or traders cut or remove teeth, a process that almost invariably leads to the animal’s death. If confiscated, reintroduction to the wild has proven difficult. Animals with no teeth are not viable candidates, and in a two-year study of 11 healthy radio-collared animals released, only two are known to have survived (Moore 2012).

Hybridization poses a real threat both on Java and elsewhere. Some taxa of slow loris are known to hybridize in zoos. Javan Slow Lorises have been observed on animal markets outside Java (e.g. Medan, Bandar Lampung on Sumatra) and other Indonesian slow loris species (N. coucang, N. menagensis) have been observed to Javan markets. Due to the morphological similarity of Nycticebus spp. misidentification is rife. Furthermore, there is a general feeling that ‘if it is a slow loris, release it.’ Not only does this pose welfare risks to the individual, but also translocated individuals may harbour infections and parasites, and could potentially hybridize (Nekaris et al. 2008, Schulze and Groves 2004).

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Management

Conservation Actions

Conservation Actions

This species is protected by Indonesian law (No. 5 of 1990) and is listed on CITES Appendix I. It is currently represented in three captive collections (Jakarta, Indonesia; Singapore; Saitama Children’s Zoo, Japan); it should be noted the specimen in Prague Zoo is in fact a N. coucang. There is no viable captive breeding programme, and reproduction in captivity is known to be difficult. Some ecological studies with conservation education components have been completed or are in progress. Training workshops have been conducted to provide law enforcement officers, CITES officials and zoo and rescue centre personnel with improved identification skills to identify Nycticebus spp. within the pet trade. Several rescue centres in the region maintain facilities for confiscated individuals. Numerous attempts have been made to release slow lorises, both monitored and unmonitored, but until more is known about the complexities of taxonomy and ecology of lorises within the region, whether or not these releases make a positive contribution to conservation remains to be seen.

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Wikipedia

Javan slow loris

The Javan slow loris (Nycticebus javanicus) is a strepsirrhine primate and a species of slow loris native to the western and central portions of the island of Java, in Indonesia. Although originally described as a separate species, it was considered a subspecies of the Sunda slow loris (N. coucang) for many years, until re-assessments of its morphology and genetics in the 2000s resulted in its promotion to full species status. It is most closely related to the Sunda slow loris and the Bengal slow loris (N. bengalensis). The species has two forms, based on hair length and, to a lesser extent, coloration.

Its forehead has a prominent white diamond pattern, which is formed by a distinct stripe that runs over its head and forks towards the eyes and ears. The Javan slow loris weighs between 565 and 687 g (1.246 and 1.515 lb) and has a head-body length of about 293 mm (11.5 in). Like all lorises it is arboreal, and moves slowly across vines and lianas instead of jumping from tree to tree. Its habitat includes primary and secondary forests, but it can also be found in bamboo forests, mangrove forests, and on chocolate plantations. Its diet typically consists of fruit, tree gum, lizards and eggs. It sleeps on exposed branches, sometimes in groups, and is usually seen alone or in pairs.

The Javan slow loris population is in sharp decline because of poaching for the exotic pet trade. It is also used in research associated with traditional medicine. Remaining populations have low densities, and habitat loss is a major threat. For these reasons the International Union for Conservation of Nature (IUCN) lists its status as "critically endangered", and it is also been included on the 2008–2010 list of "The World's 25 Most Endangered Primates". It is protected by Indonesian law and, since June 2007, is listed under CITES Appendix I. Despite these protections, as well as its presence in several protected areas, poaching continues; the wildlife protection laws are rarely enforced at the local level.

Taxonomy and phylogeny[edit]

The Javan slow loris (Nycticebus javanicus) was first described scientifically in 1812, by the French naturalist Étienne Geoffroy Saint-Hilaire.[5] The species name javanicus refers to its place of origin. However, the species was not recognized for long; by 1840, René Primevère Lesson classified it as one of several varieties of a single species of slow loris, which he called Bradylemur tardigradus.[6] In 1921, Oldfield Thomas named a second species of slow loris from Java, Nycticebus ornatus.[7]

In his 1971 review of slow loris taxonomy, taxonomist and primatologist Colin Groves recognized the Javan slow loris as a subspecies, Nycticebus coucang javanicus, of the Sunda slow loris (N. coucang), with ornatus as a synonym.[8] It was first recognized as a distinct species again in a 2000 Indonesian field guide on primates by Jatna Supriatna and Edy Hendras Wahyono.[9] In 2008, Groves and Ibnu Maryanto promoted it to species status, based on an analysis of cranial morphology and characteristics of pelage.[10] Molecular analysis of DNA sequences of the D-loop and cytochrome b genes demonstrated it to be genetically distinct from other slow loris species; phylogenetically, it is sister to a clade containing the Bengal slow loris (N. bengalensis) and the Sunda slow loris.[11] Due to its close resemblance to neighboring slow loris species, even rescue centers have been known to misidentify it.[1]

There are two forms of the Javan slow loris, distinguished mainly by differences in hair length. These have occasionally been recognized as separate species, N. javanicus and N. ornatus, but are currently both classified as a single species, although their exact taxonomic status remains unclear.[1][12][13]

Anatomy and physiology[edit]

The Javan slow loris weighs between 565 and 687 g (1.246 and 1.515 lb)[14] and is similar in appearance to the largest slow loris, the Bengal slow loris. Its face and back are marked with a distinct stripe that runs over the crown and forks, leading to the eyes and ears, which leaves a white diamond pattern on the forehead.[15] Its color is yellowish-gray. In contrast, its head, neck, and shoulders have cream hues. Like the Bornean slow loris (N. menagensis), it lacks the second incisor (I2) in its dentition.[16]

A Javan slow loris clings perpendicularly to a vertical strand of bamboo.
The Javan slow loris has a distinct stripe that runs the length of its back and forks at the crown, leading to the eyes and ears.

The Javan slow loris is larger than both of the other Indonesian slow lorises, the Sunda slow loris and the Bornean slow loris.[16] Based on averages determined from six specimens obtained from the illegal wildlife trade in Java, other morphometric parameters are as follows: head length, 59.2 mm; muzzle length, 19.9 mm; head breadth, 43.6 mm; body breadth, 250.8 mm; head and body length, 293.1 mm; chest girth, 190.8 mm; dark percentage girth (girth measurement of zone with dark dorsal hair, measured as a percent of girth circumference), 48.0 mm; neck circumference, 136.7 mm; tail length, 20.4 mm; humerus length, 67.2 mm; radius length, 71.8 mm; femur length, 83.2 mm; tibia length, 85.9 mm; hand span, 59.1 mm; foot span, 70.3 mm; and ear length, 16.8 mm.[17]

The ornatus morphotype is most reliably distinguished by its longer fur, averaging 26.8 mm compared to 22.4 mm in javanicus.[18] Other distinguishing characteristics include overall color (generally light brown in ornatus compared with brown to reddish in javanicus), and amount of brown coloring in the fur (ornatus has less brown than javanicus, resulting in a lighter-colored ventral region).[19]

In the 1860s, the brain of the Javan slow loris was examined by William Henry Flower, a comparative anatomist who specialized in the primate brain. In addition to detailing the organization, shape, and measurements of its brain, he noted that the form and surface markings were comparable to that of lemurs. He argued against grouping strepsirrhines with Insectivora (a now-abandoned biological grouping) and noted that the brain had features transitional between other primates and "inferior" mammals such as bats and carnivorans.[20]

Behavior and ecology[edit]

Like other lorises, the Javan slow loris is nocturnal and arboreal, relying on vines and lianas.[1] However, the animal has been observed moving on the ground to cross open spaces in disturbed habitat.[21] It moves through the canopy at heights between 3 and 22 m (9.8 and 72.2 ft) and is often encountered at heights between 1.5 and 9.5 m (4.9 and 31.2 ft).[1]

The Javan slow loris will eat fruit, lizards, eggs, and chocolate seeds.[21] It is also known to eat the gum of trees of the genus Albizia, in the legume family, Fabaceae, as well as from the palm genus Arenga (family Arecaceae).[22] Javan slow lorises are seen alone or in pairs and are sometimes found sleeping in groups. Instead of sleeping in nest holes, they sleep curled up on branches.[21] Like other slow lorises, the Javan slow loris has a distinctive call that resembles a high-frequency whistle.[23] The species is a host for the parasitic flatworm, Phaneropsolus oviforme.[24]

Distribution[edit]

The species is found only on the western and central portion of the island of Java in Indonesia.[1] Its presence has been confirmed in the Dieng Mountains, and it is known to be found in low densities at Gunung Gede Pangrango National Park (in montane cloud forests) and Mount Halimun Salak National Park, often only where human disturbance is minimal.[21] It inhabits both primary and secondary disturbed forest, and can be found from sea level to 1,600 m (5,200 ft), although it is more commonly found at higher elevations since lower elevations tend to be deforested.[1] A study in 2000 showed that in addition to primary and secondary forest, the Javan slow loris could be found in bamboo forests, mangrove forests, and on plantations—particularly chocolate plantations. In 2008, they were observed in West Java to occupy mixed-crop home gardens, tolerating high levels of human disturbance.[21]

Conservation[edit]

Three Javan slow lorises sit curled up on the bottom of a wired cage
The Javan slow loris is commonly sold as a pet in the markets of Indonesia, despite local laws and CITES Appendix I protection.

The Javan slow loris is listed by the International Union for Conservation of Nature (IUCN) as "critically endangered," primarily due to a rapid decline in population. For the 21–24 years prior to its 2008 assessment by the IUCN—which corresponds to three generations for the species—its numbers had dropped by at least 50%.[1] Population data for the species is sparse,[25] but a few studies have shown a low population density of 0.20 to 0.02 individuals per km2.[1]

Its numbers are still decreasing, primarily because of poaching. In Indonesia, it is sometimes used in traditional medicine, because of myths of it having magical and curative properties, but it is more frequently sold as an exotic pet.[1][26] The species is easily captured because of its slow movement, nocturnal habits, and its tendency to sleep on exposed branches. They are both actively sought for the pet trade and collected opportunistically when felling forests. Its habitat is also in decline, although most of the habitat loss occurred by the mid-1980s.[1] Within its range, human land use is intense.[27] Environmental niche modelling indicates that the Javan slow loris is more threatened by habitat loss than other slow loris species.[25] For these reasons, the Javan slow loris has been included on "The World's 25 Most Endangered Primates" published by the IUCN Species Survival Commission Primate Specialist Group (IUCN/SSC PSG), the International Primatological Society (IPS), and Conservation International (CI).[28]

Along with all other slow lorises, the Javan slow loris was elevated from CITES Appendix II to CITES Appendix I in June 2007, offering it increased protection from commercial trade.[29] It is also protected by Indonesian law, but according to loris researchers Nekaris and Jaffe, "effective law enforcement with respect to wildlife protection laws is all but non-existent in Indonesia".[17] The species can be found in several protected areas, but its numbers are uncertain. Captive collections of the Javan slow loris can be found in Prague, Czech Republic, Jakarta, Indonesia, and Singapore.[1]

References[edit]

  1. ^ a b c d e f g h i j k l Nekaris, K.A.I. , Shekelle, M, Wirdateti, Rode, E.J. & Nijman, V. (2013). "Nycticebus javanicus". IUCN Red List of Threatened Species. Version 2013.2. International Union for Conservation of Nature. Retrieved 27 November 2013. 
  2. ^ "Appendices I, II and III" (PDF). Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES). 2010. 
  3. ^ Thomas 1921, p. 627.
  4. ^ Groves 2005, p. 122.
  5. ^ Saint-Hilaire 1812, p. 164.
  6. ^ Lesson 1840, pp. 240–243.
  7. ^ Thomas 1921, p. 527.
  8. ^ Groves 1971, pp. 49–51.
  9. ^ Supriatna & Wahyono 2000, pp. 19–24.
  10. ^ Groves & Maryanto 2008, p. 120.
  11. ^ Chen et al. 2006, pp. 1197–1198.
  12. ^ Nekaris & Jaffe 2007, p. 192.
  13. ^ Thomas 1921, p. 628.
  14. ^ Nekaris, Blackham & Nijman 2008, p. 734.
  15. ^ Nekaris et al. 2009, p. 44.
  16. ^ a b Groves 1971, p. 49.
  17. ^ a b Nekaris & Jaffe 2007, p. 191.
  18. ^ Nekaris & Jaffe 2007, p. 188.
  19. ^ Nekaris & Jaffe 2007, p. 193.
  20. ^ Gray 1862, pp. 103–105.
  21. ^ a b c d e Nekaris & Munds 2010, p. 388.
  22. ^ Nekaris et al. 2010, p. 157.
  23. ^ Nekaris, Blackham & Nijman 2008, p. 743.
  24. ^ Dawes 2011, p. 384.
  25. ^ a b Nekaris & Munds 2010, pp. 383–384.
  26. ^ Nekaris et al. 2010, p. 877.
  27. ^ Thorn et al. 2009, p. 295.
  28. ^ Nekaris et al. 2009, pp. 44–46.
  29. ^ McGreal 2007, p. 15.

Literature cited[edit]

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