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

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susceptible to N. neesiana invasion. For example “few weed species have successfully established and persisted” in the<br />

<strong>Australia</strong>n Alps, the number declining with increasing altitude (McDougall and Walsh 2007 p. 44). Excluded formations include<br />

aforementioned wetland formations and maritime <strong>grass</strong>lands, the Western Slopes Grasslands <strong>of</strong> NSW including Moore’s (1993)<br />

Xerophytic Mid<strong>grass</strong> (Southern) and Saltbush Xerophytic Mid<strong>grass</strong>, Eastern Victorian highlands <strong>grass</strong>lands (e.g. Lake Omeo),<br />

high altitude <strong>grass</strong>lands <strong>of</strong> the Monaro region <strong>of</strong> NSW, and alpine <strong>grass</strong>lands and meadows. The <strong>grass</strong>lands that once existed<br />

around the shores <strong>of</strong> Lake Omeo (Benambra area) were similar to those <strong>of</strong> the Southern Tablelands and were dominated by T.<br />

triandra (Lunt et al. 1998) or Austrodanthonia (Kirkpatrick et al. 1995), but show clear affinities with high altitude <strong>grass</strong>lands<br />

(Carter et al. 2003). According to Kirkpatrick et al. (1995) the Lake Omeo <strong>grass</strong>lands are probably derived from Eucalyptus<br />

pauciflora Sieber ex Spreng. woodland.<br />

The natural occurrence <strong>of</strong> temperate <strong>grass</strong>lands in south-eastern <strong>Australia</strong> was determined by relatively low rainfall (in the range<br />

<strong>of</strong> 350-1000 mm mean annual, mainly 500-600 mm), flat to undulating topography, and soils that were poorly drained, heavytextured<br />

and moderately to highly fertile (Mott and Groves 1994, Sharp 1997, Jones 1999b, Lunt and Morgan 2002). The<br />

geological parent materials produce soil with a high clay content (Jones 1999b). Heavy clay or clay loam soils, and a relatively<br />

dry, cold climate “are prerequisites for <strong>grass</strong>land vegetation worldwide” (Benson and Redpath 1997 p. 307). South-eastern<br />

<strong>Australia</strong>n <strong>grass</strong>lands generally occur on younger soils that have not been heavily leached or become lateritic or infertile, and<br />

thus tend to occur where the parent rocks have weathered in situ and there is little erosion, and the soils are relatively fertile<br />

(Jones 1999b). Most <strong>grass</strong>land soils have a high water content but low water availability because the clay minerals bind water,<br />

and there is little pore space (Jones 1999b).<br />

Some temperate <strong>Australia</strong>n <strong>grass</strong>lands occurred in the drier areas down to c. 250 mm annual rainfall on the arid margins <strong>of</strong><br />

chenopod shrublands (Mack 1989) although these are probably better categorised as semi-arid formations (Carter et al. 2003). In<br />

the <strong>Australia</strong>n Alps, <strong>grass</strong>lands are generally found on deep humus soils in valley bottoms subject to cold air accumulation and<br />

frosts (McDougall andWalsh 2007).<br />

Causes <strong>of</strong> treelessness<br />

Heavy-textured clay substrates dry out and crack deeply in summer (c. 13% on an areal basis according to Patton 1935) and this<br />

may prevent the establishment <strong>of</strong> trees and shrubs, as may fire, which occurs ubiquitously (Groves and Whalley 2002). Moore<br />

(1993 p 353) explained treelessness to be the result <strong>of</strong> “shallow penetration <strong>of</strong> water in environments with relatively low rainfall<br />

and high evaporation, where tree seedlings would be subjected to intense competition for surface-rooted <strong>grass</strong>es and other<br />

herbaceous species” and in wetter areas “poor aeration following temporary waterlogging after winter rains”. Patton (1935 p.<br />

175) argued that trees can be established artificially on the Victorian basalt plains by “opening up the ground and ... destroying<br />

the native vegetation”, so concluded that the native vegetation itself prevented the establishment <strong>of</strong> tree seedlings. Elsewhere<br />

however he argued that heavy textured soils inhibit free entry <strong>of</strong> water, have slow percolation and bad aeration, that summer<br />

cracking leads to deep drying, and that deep rooting is difficult, so it is the physical characteristics <strong>of</strong> the soil, accentuated by the<br />

evenness <strong>of</strong> contour in the plains that determines their treelessness (Patton 1930). Barlow and Ross (2001) argue that multiple,<br />

confounded, variable factors are responsible, with soil charcteristics, particularly drainage, the most important and subsidiary<br />

influences from climate and fire. In a trial in the South American pampas competition from tussock <strong>grass</strong>es prevented<br />

establishment <strong>of</strong> half the tree species tested (Aguiar 2005). Kirkpatrick et al. (1995) more or less concurred: tree seedlings are<br />

largely excluded by competition in dense <strong>grass</strong>land swards, which may use all the available soil moisture, and severe<br />

disturbances such a soil digging are required for trees to establish.<br />

In the Volcanic Plains Grasslands <strong>of</strong> western Victoria, where ever any other geological formation abuts basalt, trees occur.<br />

Eucalyptus camaldulensis grows, for example, where granodiorite is exposed or eroded out <strong>of</strong> the basalt (Patton 1930). The<br />

granite <strong>of</strong> the You Yangs provides another notable example. Soil chemistry, as well as structure can determine treelessness: soils<br />

dominated by sodium, common in northern Victoria, usually lack trees (Jones 1999b).<br />

Distribution <strong>of</strong> <strong>grass</strong>lands in the ACT is determined by accumulation <strong>of</strong> cold air pockets in valley floors, creating conditions that<br />

are too cold to permit growth <strong>of</strong> trees and shrubs (Chan 1980), but low rainfall, heavy-textured soils and the legacy <strong>of</strong> aboriginal<br />

fire regimes are also important (Sharp 1997). Very low temperatures associated with nocturnal temperature inversions have been<br />

invoked as the cause <strong>of</strong> treelessness in subalpine valleys (Moore 1993).<br />

Lowland <strong>grass</strong>lands<br />

The term “lowland” <strong>grass</strong>lands, considered to include those formations at altitudes below 1000 m, has been widely used (Lunt<br />

1991, McDougall and Kirkpatrick 1993, Kirkpatrick et al. 1995, Sharp 1994, Lunt et al. 1998). Prior to European occupation<br />

they probably covered c. 2 million ha, <strong>of</strong> which “perhaps” 10,000 ha survived in “more or less natural” condition by 1992<br />

(Kirkpatrick et al. 1995 p. 8). Classifications <strong>of</strong> lowland <strong>grass</strong>lands have varied between authors and government authorities and<br />

have not always coincided. The New South Wales classification <strong>of</strong> Benson (2004) has four classes covering sub-humid<br />

<strong>grass</strong>lands, including the Temperate Montane Grasslands, found in the south-east, which include high altitude formations<br />

dominated by Poa spp. Such <strong>grass</strong>lands, including those on the Monaro Plains <strong>of</strong> NSW, are generally excluded from the<br />

‘lowland’ category by most authors. The change from lowland to montane and alpine <strong>grass</strong>lands is gradual and clinal, so 1000 m<br />

is an arbitrary delimination (see discussion in Carter et al. 2003).<br />

Secondary and derived <strong>grass</strong>lands<br />

‘Secondary <strong>grass</strong>land’ is derived from other vegetation formations, <strong>of</strong>ten in <strong>Australia</strong> from <strong>grass</strong>y woodland in which trees have<br />

been cleared and on which livestock are grazed (Moore 1993, Mott and Groves 1994, Groves and Whalley 2002). Temperate<br />

<strong>grass</strong>y woodlands are also a threatened vegetation type (Benson 2004, Keith 2004, McIntyre and Lavorel 2007) and their <strong>grass</strong>y<br />

stratum may be indistinguishable, for practical conservation purposes, from that <strong>of</strong> adjoining natural <strong>grass</strong>land (Carter et al.<br />

2003, Keith 2004). Indeed Moore (1993 p. 343) considered that most <strong>of</strong> his Temperate Short<strong>grass</strong> communities, including most<br />

<strong>of</strong> the Western Basaltic Plains <strong>of</strong> Victoria, the NSW Riverina and Gippsland Plains, to be “mostly the understoreys <strong>of</strong> temperate<br />

woodlands modified by clearing and grazing by livestock and rabbits”. The <strong>grass</strong>lands derived from temperate <strong>grass</strong>y woodlands<br />

are frequently also very similar floristically to natural <strong>grass</strong>lands ( Mott and Groves 1994) and can have the same ecological<br />

95

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