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Pheasants: Status Survey and Conservation Action Plan ... - IUCN

Pheasants: Status Survey and Conservation Action Plan ... - IUCN

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Taxonomy: The crested argus is represented by two<br />

subspecies that occupy widely separated geographical<br />

ranges. These two forms are morphologically distinct<br />

(Delacour 1977), <strong>and</strong> their specific taxonomic status <strong>and</strong><br />

validity requires assessment using other criteria (e.g. DNA<br />

sequence comparisons).<br />

Range <strong>and</strong> population: The crested argus is endemic to<br />

Southeast Asia. The nominate subspecies ocellata occurs<br />

along the Annamite Mountain chain in central <strong>and</strong> southern<br />

Vietnam <strong>and</strong> neighbouring eastern Laos (Duckworth et al.<br />

1999), south to the Da Lat Plateau in southern Vietnam<br />

(Robson et al. 1993b). The subspecies nigrescens is restricted<br />

to seven sites within or very close to Taman Negara in<br />

central Peninsular Malaysia (Mamat <strong>and</strong> Yasak 1998).<br />

Although its range <strong>and</strong> habitat have been reduced <strong>and</strong><br />

fragmented in Laos <strong>and</strong> Vietnam, <strong>and</strong> a substantial<br />

population decline has occurred there, the nominate<br />

subspecies is still relatively widespread <strong>and</strong> locally common<br />

(Robson et al. 1991, Tobias et al. 1998, Duckworth et al.<br />

1999).<br />

Ecology: In Laos <strong>and</strong> Vietnam, it is resident in primary,<br />

logged, <strong>and</strong> secondary evergreen forest from sea-level up<br />

to 1,500m, <strong>and</strong> from 1,700m–1,900m on the Da Lat Plateau<br />

(Robson et al. 1991, 1993b). It occurs at highest densities<br />

in moist primary forest in lowl<strong>and</strong>s, up to about 900m<br />

(Tobias 1997, Thewlis et al. 1998, Duckworth et al. 1999).<br />

In Malaysia, it inhabits tall hill dipterocarp/lower montane<br />

transitional forest, generally from about 800–1,100m<br />

(Davison 1977, 1978b, 1979).<br />

Threats: The Indochinese population is probably most at<br />

risk from continuing forest loss <strong>and</strong> degradation, both<br />

within <strong>and</strong> outside protected areas. The greatest problems<br />

stem from commercial logging, various forms of illegal<br />

timber extraction, clearance for agricultural plantations<br />

<strong>and</strong> shifting cultivation (Nguyen Cu <strong>and</strong> Eames 1993,<br />

Robson et al. 1991, Lambert et al. 1994), <strong>and</strong> road building<br />

(Tobias 1997, Tobias et al. 1998). Disturbance <strong>and</strong> snaring<br />

(primarily for food) at display arenas pose more significant<br />

threats than deforestation in some areas (Lambert et al.<br />

1994, Timmins <strong>and</strong> Evans 1996, Thewlis et al. 1998,<br />

Duckworth et al. 1999). The Malaysian population is less<br />

threatened, being almost entirely encompassed within<br />

Taman Negara where the main threat is limited habitat<br />

loss on the periphery of the park (e.g., Gunung Rabung)<br />

(P.J.K. McGowan in litt.).<br />

<strong>Conservation</strong>: CITES Appendix I. It occurs in numerous<br />

protected areas, including Bach Ma National Park, at least<br />

10 nature reserves in Vietnam, <strong>and</strong> at least two designated<br />

<strong>and</strong> two proposed national biodiversity conservation areas<br />

in Laos. The Malaysian population’s range falls almost<br />

entirely within Taman Negara National Park.<br />

Targets:<br />

• <strong>Survey</strong> suitable habitat in Laos <strong>and</strong> Vietnam to clarify<br />

its current distribution <strong>and</strong> assess relative abundance in<br />

relation to habitat degradation.<br />

• Monitor the Malaysian population <strong>and</strong> selected<br />

populations in Laos <strong>and</strong> Vietnam regularly.<br />

• Promote strict enforcement of hunting regulations in<br />

protected areas supporting populations in Indochina, in<br />

combination with locally targeted conservation awareness<br />

initiatives.<br />

• Conduct taxonomic research into the relationship between<br />

the Malaysian <strong>and</strong> Indochinese populations.<br />

Congo peafowl<br />

(Afropavo congensis)<br />

Vulnerable C2a<br />

This species is assumed to have a small population. Recent<br />

surveys suggest that large areas within its range are<br />

unoccupied implying that the population is severely<br />

fragmented. Hunting <strong>and</strong> habitat loss continue unabated<br />

<strong>and</strong> the population is, therefore, inferred to be declining.<br />

These circumstances lead to its classification as Vulnerable.<br />

Taxonomy: This is the only pheasant species native to<br />

Africa.<br />

Range <strong>and</strong> population: The Congo peafowl occurs in the<br />

eastern Democratic Republic of Congo (DRC). Research<br />

in 1993–95 confirmed its presence in 13 of the 20 survey<br />

areas, though it did not find the species abundant in any.<br />

This work also identified new sites that significantly extend<br />

the species’ range northeast into the Ituri Forest (Hart<br />

<strong>and</strong> Upoki 1997). Subsequently, it was also located north<br />

of the Lomako River <strong>and</strong> along the Yekokora River<br />

(Dupain <strong>and</strong> van Krunkelsven 1996), as well as further<br />

south between the Lukenie <strong>and</strong> Sankuru Rivers<br />

(Thompson 1996). Forest between the Lomami <strong>and</strong> Congo<br />

Rivers may also hold significant concentrations, but<br />

information from this area remains limited (Hart <strong>and</strong><br />

Upoki 1997).<br />

Ecology: It occurs in many different forest types, but is<br />

often associated with slopes between watersheds with<br />

shallow soils supporting dry forest <strong>and</strong> an open<br />

understorey. Its sparse <strong>and</strong> irregular distribution may<br />

correspond, in part, to the limited availability of this<br />

habitat type. It does not appear to have a specialised diet,<br />

<strong>and</strong> has been recorded eating fruit from common tree<br />

species throughout the region (Hart <strong>and</strong> Upoki 1997), as<br />

well as aquatic insects <strong>and</strong> termites. The breeding<br />

season may depend on local rainfall conditions (McGowan<br />

1994a).<br />

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