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Recovery plan for the brush-tailed rock-wallaby - Department of ...

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Approved NSW <strong>Recovery</strong> Plan Brush-<strong>tailed</strong> <strong>rock</strong>-<strong>wallaby</strong><br />

Main (1961) and Main and Yadav (1972) investigated <strong>the</strong> difference in black-footed <strong>rock</strong><strong>wallaby</strong><br />

(Petrogale lateralis) populations on a group <strong>of</strong> islands <strong>of</strong>f Dampier on <strong>the</strong> north-western<br />

coast <strong>of</strong> Western Australia. The original population on <strong>the</strong> fox-free Enderby Island was<br />

estimated to be 1500 animals while Dolphin Island (<strong>of</strong> similar size to Enderby but with foxes and<br />

feral cats present), had an estimated population <strong>of</strong> 50. After fox control on Dolphin Island, <strong>the</strong>re<br />

was an almost 30-fold increase in <strong>the</strong> density <strong>of</strong> <strong>rock</strong>-wallabies. Nearby Depuch Island was<br />

surveyed in 1962 by <strong>the</strong> Western Australian Museum, and at that time many black-footed <strong>rock</strong>wallabies<br />

were present, but <strong>the</strong>re was much evidence <strong>of</strong> fox predation which had only recently<br />

arrived on <strong>the</strong> island. Twenty years later, <strong>the</strong>re was no trace <strong>of</strong> <strong>rock</strong>-wallabies on Depuch Island.<br />

The long history <strong>of</strong> circumstantial evidence implicating <strong>the</strong> fox, combined with <strong>the</strong>ir own<br />

suspicions <strong>of</strong> fox involvement in black-footed <strong>rock</strong>-<strong>wallaby</strong> decline, led Kinnear et al (1988 and<br />

1998) to attempt to gain more evidence. Their work concluded that <strong>the</strong> fox was a significant<br />

factor in <strong>the</strong> demise and decline <strong>of</strong> native mammals, but that <strong>rock</strong>-wallabies can recover even<br />

under serious fox predation. The validity <strong>of</strong> <strong>the</strong>se conclusions has been critiqued (e.g. by Hone<br />

1994 and 1999). Debate over <strong>the</strong> conclusions drawn from this study shows <strong>the</strong> importance <strong>of</strong><br />

testable hypo<strong>the</strong>ses, in this case, <strong>the</strong> need to monitor predator numbers as well as prey numbers<br />

to be able to demonstrate <strong>the</strong> reasons behind measured population changes.<br />

Hornsby (1982) has reported a juvenile wallaroo (Macropus robustus) falling prey to a fox.<br />

Studies by Banks (1997) and Banks et al (2000) on foxes and predation on native mammals and<br />

rabbits at Namadgi National Park have strongly indicated that juvenile mortality in eastern grey<br />

kangaroos (M. giganteus) was caused by fox predation. These studies also suggest eastern grey<br />

kangaroos alter <strong>the</strong>ir behaviour in response to threats from foxes. This is consistent with Kinnear<br />

et al’s 1998 finding that predation pressure can alter habitat use and <strong>for</strong>aging behaviour in blackfooted<br />

<strong>rock</strong>-wallabies.<br />

Although foxes have been implicated in <strong>the</strong> decline <strong>of</strong> macropods in Western Australia, <strong>the</strong>re is<br />

limited documented evidence <strong>of</strong> <strong>the</strong> impact <strong>of</strong> foxes on <strong>the</strong> BTRW. There are differences<br />

between <strong>the</strong> habitat <strong>of</strong> black-footed <strong>rock</strong>-wallabies in Western Australia and <strong>of</strong> <strong>the</strong> BTRW,<br />

which could affect BTRW susceptibility to foxes. Black-footed <strong>rock</strong> wallabies live on wheat<br />

plains and <strong>rock</strong>y outcrops, whereas BTRWs live in <strong>for</strong>ests, on continuous ridgelines and in<br />

precipitous gorges.<br />

Foxes are reputedly more effective predators <strong>of</strong> <strong>rock</strong>-wallabies than dingos, actively hunting<br />

<strong>the</strong>m on cliffs (Rolls 1969 in Short 1982). Dunn (1984) speaks <strong>of</strong> <strong>the</strong> agility and climbing skill<br />

<strong>of</strong> <strong>the</strong> fox, and its ability to enter into all but <strong>the</strong> most inaccessible <strong>rock</strong>-<strong>wallaby</strong> refuges. Bayne<br />

(unpub.) observed foxes flushed into <strong>the</strong> open when on a BTRW-occupied cliff on three<br />

occasions, and twice watched foxes covering every part <strong>of</strong> a BTRW-occupied cliff and<br />

examining each ledge and cave (all <strong>the</strong>se occasions were on gorge–rim cliff colonies). Bayne<br />

also noted that on one occasion <strong>the</strong> fox successfully negotiated a short section <strong>of</strong> slab.<br />

In contrast, <strong>the</strong>re is no strong evidence <strong>for</strong> fox predation in nor<strong>the</strong>rn NSW. Of 144 fox scats<br />

collected in <strong>the</strong> vicinity <strong>of</strong> BTRW colonies in north-eastern NSW, none contained <strong>the</strong> remains <strong>of</strong><br />

a BTRW (Lunney et al 1996). In addition, <strong>of</strong> 342 scats <strong>of</strong> dog, dingo and fox examined, BTRW<br />

was identified as a prey item in only 1% (Lunney et al 1996), despite <strong>the</strong> examinations being<br />

conducted to coincide with periods <strong>of</strong> pouch emergence and juvenile dispersal, when predation<br />

on <strong>the</strong> BTRW was expected to be most likely (Lunney et al 1996).<br />

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