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Literature review: Impact of Chilean needle grass ... - Weeds Australia

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<strong>of</strong> destruction as vermin and partly from extinction <strong>of</strong> its tussock <strong>grass</strong>land habitat (Seebeck and Rose 1989). Bettongs were<br />

considered to be agricultural pest species during early European settlement (Seebeck and Rose 1989, Noble et al. 2007).<br />

Wakefield (1964a p. 277) listed other species found as subfossils in caves near Byaduk and Mt Eccles that are not found in the<br />

Western Plains Grasslands today but were “Presumably ... present on the basalts <strong>of</strong> south-western Victoria at the time <strong>of</strong><br />

European occupation ...”. These included the extinct Pseudomys auritus which was present “in the recent past ... eastward,<br />

apparently in abundance, to central Victoria” (Wakefield 1964a p. 278) and was “once widespread in western Victoria”<br />

(Wakefield 1963b p. 44).<br />

Perhaps at a more distant time the Western Basalt Plains were also inhabited by the Tasmanian Devil Sarcophilus harrisii<br />

(Boitard) and the Thylacine Thylacinus cyanocephalus (Harris). Wakefield (1963a) reported sub-fossil remains <strong>of</strong> both these<br />

large predators, extinct on mainland <strong>Australia</strong>, from lava caves at Mount Hamilton. Remains <strong>of</strong> <strong>of</strong> S. harrisii appeared to be<br />

“quite modern” with one mandible having “pieces <strong>of</strong> dried tissue adhering to the bone”, while the few remains <strong>of</strong> T.<br />

cyanocephalus appeared to be “not ... very old” (Wakefield 1963a p. 324). Remains <strong>of</strong> the latter species are known also in<br />

Victoria from Gisborne, while remains <strong>of</strong> S. harrisii in Victoria have been radiocarbon dated to 550 ±200 years B.P. (Wakefield<br />

1963a). Dixon (1989 p. 557) noted that T. cyanocephalus was well known from the main area <strong>of</strong> natural open <strong>grass</strong>lands in<br />

Tasmania, the midland plains region, and that most captures <strong>of</strong> the animal occured in “farmed flat areas”, where it was<br />

considered a serious predator <strong>of</strong> lambs. Loss <strong>of</strong> ‘top predators’ has serious cascade effects in food webs, and probably<br />

contributed greatly to the collapse <strong>of</strong> <strong>grass</strong>land ecosystems.<br />

Bandicoots are primarily nocturnal and crepuscular, rat to rabbit sized marsupials, which, along with bilbies (Thylacomyiidae)<br />

have sufferred more negative impact from European occupation than any other marsupial group except Potoroidae (Brown 1987)<br />

and the thylacine. The extinct Pig-footed Bandicoot Chaeropus ecaudatus (Peramelidae) was a <strong>grass</strong>land species which required<br />

“lush growing tips <strong>of</strong> <strong>grass</strong>es and herbs”, so livestock grazing is probably the major factor in its extinction (Menkhorst 1995a)<br />

along with habitat destruction by rabbits and predation by introduced mammals (Seebeck and Mansergh 2003). Seebeck and<br />

Mansergh (2003), on the other hand, considered it to be an arid zone species, restricted in the historical period in Victoria to the<br />

Mallee. Sheep grazing is also probably the major factor in disappearance <strong>of</strong> the Bridled Nailtail Wallaby (Menkhorst 1995a).<br />

Losses <strong>of</strong> such a large proportion <strong>of</strong> the native herbivores likely had a pr<strong>of</strong>ound effect on plant diversity (Bloomfield and<br />

McPhee 2006).<br />

Studies <strong>of</strong> more arid and northern regions <strong>of</strong>/<strong>Australia</strong>, and other areas <strong>of</strong> the temperate pastoral zone show similar losses <strong>of</strong><br />

medium sized (35 g to 55 kg) ground dwelling marsupials and murid rodents (Burbidge and McKenzie 1989, Short and Smith<br />

1994, Short and Turner 1994, Noble et al. 2007). Various factors in combination are blamed including hunting, increased<br />

predation from foxes and cats, rabbit and livestock grazing, habitat clearance and fragmentation, land use change and altered fire<br />

regimes (Recher and Lim 1990, Short and Smith 1994). Rat kangaroos (Potoroidae) never recovered from hunting under a<br />

bounty system on the Northern Tablelands <strong>of</strong> NSW (Johnson and Jarman 1975), although they were present “in plague<br />

proportions” in the 1880s and 1890s (Cameron 1975 p. 21). Altered fire regimes are possibly the most important: in areas where<br />

it has been possible to study the losses, in Central <strong>Australia</strong>, they are temporally correlated with the departure <strong>of</strong> aboriginal<br />

people and the cessation <strong>of</strong> regular aboriginal burning (Short and Turner 1994, Flannery 1994). The absence <strong>of</strong> regular burning<br />

resulted in decreased rates <strong>of</strong> nutrient recycling and the absence <strong>of</strong> new lush vegetation, creating a nutritional crisis for the more<br />

specialised feeders (Flannery 1994). A general increase in biomass <strong>of</strong> vegetation coupled with decreased patchiness meant that a<br />

fire, when it did arrive, burnt much more widely and intensely than previously, creating large areas with no food, nor shelter<br />

from predators, and later a uniform, even-aged vegetation (Flannery 1994). However a test <strong>of</strong> the mosaic burning decline<br />

hypothesis (Short and Turner 1994) found that mosaic scale had no significant effect on survival <strong>of</strong> three species in the critical<br />

weight range, and that declines on mainland <strong>Australia</strong> and survival on <strong>of</strong>f-shore islands was better explained by the presence or<br />

absence <strong>of</strong> exotic predators (foxes and cats) and herbivores (rabbits and livestock). More generally, Burbidge and McKenzie<br />

(1989) found that the diverse effects <strong>of</strong> diversion <strong>of</strong> environmental production to human uses effectively resulted in a general<br />

trend to environmental aridity, that differentially affected moderately sized mammals with limited mobility, relatively high daily<br />

metabolic requirements and more specialised feeding strategies.<br />

Victorian <strong>grass</strong>lands now support little native mammalian diversity. Victorian mammals adapted to <strong>grass</strong>lands and <strong>grass</strong>y<br />

woodlands are one <strong>of</strong> Menkhorst’s (1995b) five groups <strong>of</strong> mammals requiring specific managment to secure their future. They<br />

include the Fat-tailed Dunnart Sminthopsis crassicaudata (Gould), Eastern Barred Bandicoot Perameles gunnii and Common<br />

Wombat Vombatus ursinus. The latter occurred throughout the volcanic plains in the 1800s but is now extinct in western<br />

Victorian <strong>grass</strong>lands. Another widespread species not threatened on a State or national basis, the Eastern Grey Kangaroo<br />

Macropus giganteus was once common in the Victorian basalt plains (Sutton 1916-1917, Coutts 1982) but is now rare in the<br />

region (Lunt et al. 1998) although some large populations exist (e.g. at Woodlands Historic Park). In the South East <strong>of</strong> South<br />

<strong>Australia</strong> it was restricted to four colonies by 1983, one in woodland with associated <strong>grass</strong>land (Aitken 1983). The Western Grey<br />

Kangaroo M. fuliginosus (Desmarest) was still common and included <strong>grass</strong>land in its habitat (Aitken 1983). This species prefers<br />

areas with heathy understorey but forages in <strong>grass</strong>land (Bennett 1995).<br />

In the South East <strong>of</strong> South <strong>Australia</strong> S. crassicaudata was considered common in <strong>grass</strong>land, including pasture, while V. ursinus<br />

was reduced to remnants, including populations in coastal <strong>grass</strong>land and sedgeland (Aitken 1983).<br />

Perameles gunnii, incorrectly said to be endemic to the Victorian Volcanic Plain (DNRE 1997), was formerly widespread and<br />

abundant across the Plains from near Melbourne north to Beaufort and west to Coleraine in Victoria and into the South East <strong>of</strong><br />

South <strong>Australia</strong>, but is now critically endangered on mainland <strong>Australia</strong> (Aitken 1983, Brown 1987, Brown et al. 1991,<br />

Backhouse and Crossthwaite 2003). The mainland and Tasmanian populations are distinct, undescribed subspecies (Backhouse<br />

and Crossthwaite 2003). P. gunnii is “specifically adpated to <strong>grass</strong>land and savannah woodland” (Brown 1987). P. gunnii digs<br />

small conical burrows in the soil when foraging for its invertebrate prey. Earthworms are important in the diet in wetter months.<br />

Cockroaches (Blattidae), earwigs (Forficulidae), beetles, both larval and adult especially larval Scarabaeidae, Lepidoptera larvae<br />

and Romulea rosea bulbs are other common dietary items (Brown 1987).<br />

144

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