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

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In <strong>Australia</strong> the altitudinal range is from near sea level (e.g. in the Altona area near Melbourne) to c. 1200-1400 m at Guyra on<br />

the Northern Tablelands <strong>of</strong> NSW (Gardener et al. 2005). In the Sydney region it is found from 0-600 m (Benson and McDougall<br />

2005).<br />

Climate<br />

Stipeae are generally classic xeromorphs or mesic, Austrostipa aristiglumis (F.Muell.) S.W.L. Jacobs and J. Everett and<br />

Trikeraia being exceptions (Arriaga and Jacobs 2006). In south-eastern South America members <strong>of</strong> the tribe increase with<br />

increasing latitude, being absent in the megathermic zones, a major vegetation component in mesothermic zones and dominant in<br />

Patagonia (Perelman et al. 2001). Indeed, increases <strong>of</strong> c. 15 to 23% in the average relative cover <strong>of</strong> Stipeae compared to other<br />

<strong>grass</strong> tribes has been measured across the narrow latitudinal range (c. 35-38°) <strong>of</strong> the Flooding Pampa, in Argentina (Perelman et<br />

al. 2001). The distribution <strong>of</strong> particular Stipeae, including several Nassella species, in this region shows strong latitudinal<br />

correlations, with a group including N. hyalina and N. charruana found only in the north, and others found only in the south<br />

(Perelman et al. 2001).<br />

N. neesiana is unusual in that it has a very wide climatic tolerance. It has invaded areas outside the climatic range it occupies in<br />

South America (Gardener 1998). The stronghold <strong>of</strong> N. neesiana, the pampas region, has warm, <strong>of</strong>ten humid summers, mild,<br />

usually drier winters with temperatures uncommonly below freezing, annual rainfall <strong>of</strong> 600-1000 mm, and little drought (Mack<br />

1989). In the pampas, “<strong>grass</strong> is driven out only where water is very abundant in the soil, as ... along the banks <strong>of</strong> rivers ... the<br />

climate is a perfect <strong>grass</strong>land-climate, with ... rainfall not more than moderate but well distributed ... humid, moderately warm<br />

vegetative season [and] strong winds ... with moderate atmospheric humidity ... hostile indeed to woodland” (Schimper 1903 p.<br />

459). Summer rainfall is prevalent in eastern South America south <strong>of</strong> 30° including Rio Grande do Sul, eastern Uruguay and<br />

Argentina (Schimper 1903). Restricted occurences in southern Brazil, where the <strong>grass</strong>lands are considered to be relicts <strong>of</strong> drier,<br />

cooler conditions, may be determined by the more subtropical, humid climate (Overbeck and Pfadenhauer 2007). N. neesiana is<br />

one <strong>of</strong> the dominant <strong>grass</strong>es in La Plata district <strong>of</strong> Buenos Aires where the climate is warm temperate and humid, with a mean<br />

annual temperature <strong>of</strong> 16.5 ºC and mean annual rainfall <strong>of</strong> 992 mm (Cabrera 1949). It occurs across the Flooding Pampa <strong>of</strong><br />

north-eastern Argentina which has annual rainfalls <strong>of</strong> 850-900 mm, average annual temperatures <strong>of</strong> 13.8-15.9°C and average<br />

minimum temperatures in July <strong>of</strong> 1.8-6°C (Perelman et al. 2001). It is a major <strong>grass</strong> in the Tandilia Range <strong>of</strong> south-east Buenos<br />

Aires province where the annual rainfall is about 800 mm and the mean monthly temperatures for the coldest and warmest<br />

months are 13 and 23°C (Honaine et al. 2009), and in parts <strong>of</strong> south-west Buenos Aires Province, where the climate is humid<br />

temperate with a mean annual temperature <strong>of</strong> 14.5ºC and annual average rainfall <strong>of</strong> 850 mm (Amiotti et al. 2007). It occurs in<br />

the littoral areas and lower parts <strong>of</strong> the La Plata basin where the climate lacks a marked dry season (Schimper 1903). Large tracts<br />

<strong>of</strong> northern Argentina, the base <strong>of</strong> the Andes and the Provinces <strong>of</strong> Entre Rios and Corrientes have annual rainfall <strong>of</strong> 1000-1200<br />

mm (Schimper 2003) and in those areas N. neesiana loses its dominance in <strong>grass</strong>land to species better adapted to a wetter, more<br />

subtropical climate (Soriano et al. 1992). In Uruguay N. neesiana is supposedly “resistant to adverse climates” (Gardener et al.<br />

1996b p. 3, citing Rosengurtt et al. 1970). In the Pampean province <strong>of</strong> southern Brazil the annual rainfall is in the range <strong>of</strong> c.<br />

1200-1600 mm and mean annual temperatures are 13-17°C (Overbeck et al. 2007). On the Juan Fernández Islands <strong>of</strong> Chile it<br />

grows in dry or humid areas (Baeza et al. 2007).<br />

In continental South America as a whole N. neesiana is found in the 500-1500 mm annual rainfall zones, with some extreme<br />

outliers, and its northern distribution is “limited by lack <strong>of</strong> low winter temperatures necessary for vernalization” (Gardener et al.<br />

1996b), so is restricted to higher altitudes in the tropics. It occurs in southern Chile near Valdiva where the average annual<br />

rainfall exceeds 2600 mm and maximum/minimum temperatures are 22.8/11.1 in January and 11.1/5.0ºC in July (Gardener et al.<br />

1996b). Similar seasonal temperatures occur in montane-alpine areas <strong>of</strong> south-eastern <strong>Australia</strong>, although few such areas have<br />

rainfall exceeding 1600 mm. It occurs in areas <strong>of</strong> far north-east Argentina near Posadas, where the rainfall was over 1900 mm<br />

per annum, with January and July maximum/minimum temperatures <strong>of</strong> 33.2/21.8ºC and 21.9/11.4ºC (Gardener et al. 1996b).<br />

The closest approximations to such a climate in <strong>Australia</strong> occur in the wet tropics. In western Argentina it occurs at Medoza,<br />

where the climate is very dry (223 mm) with January/July maximum/minimum temperatures <strong>of</strong> 32.0/19.4ºC and 14.7/2.4ºC<br />

(Gardener et al. 1996b), similar to some arid areas <strong>of</strong> inland southern <strong>Australia</strong>. In arid regions <strong>of</strong> South America it may only<br />

occur where the microclimate is more mesic, e.g. along rivers (Gardener et al. 1996b).<br />

In South Africa N. neesiana has been recorded in temperate summer rainfall areas (Wells et al. 1986). The climate parameters <strong>of</strong><br />

one <strong>of</strong> its stronghold areas in New Zealand are an annual average rainfall <strong>of</strong> 650-900 mm, warm summers with frequent droughts<br />

and moderate winters, conditions said to be very similar to the climate in its Argentinian range (Bourdôt and Hurrell 1989a). The<br />

900 mm isohyet has been quoted as a limiting factor in north-facing hill slopes in the Hawkes Bay area <strong>of</strong> New Zealand (Slay<br />

2002) where its potential range was considered to be “northerly facing hill country in low to medium rainfall (700-900 mm)”<br />

(Slay 2001 p. 5).<br />

In south eastern <strong>Australia</strong> N. neesiana occurs primarily in areas with 500-800 mm average annual rainfall (Muyt 2001) in a range<br />

<strong>of</strong> climates including the warm wet summer/cold dry winter <strong>of</strong> the Northern Tablelands <strong>of</strong> NSW, and hot dry summer/cold wet<br />

winter <strong>of</strong> southern Victoria (Gardener et al. 1999). In the Sydney region it is found in areas with 700-1000 mm mean annual<br />

rainfall (Benson and McDougall 2005).<br />

N. neesiana appears to be well adapted to seasonal dryness (Bourdôt and Hurrell 1987b) and is drought tolerant (Muyt 2001,<br />

McLaren et al. 2002b, Slay 2002c, Storrie and Lowien 2003). Tsvelev (1977 p. 2) thought that the small chromosomes and small<br />

pollen grains (general stipoid characters), lemma and palea structure protecting the flowers, a dense clumping habit and the<br />

presence <strong>of</strong> intravaginal shoots (as in N. neesiana) all indicated specialisation for xerophytic climates. Slay (2002a p. 10) thought<br />

that the bare ground resulting from drought was “the catalyst for seedling establishment”.<br />

Fire<br />

Fire is a feature <strong>of</strong> the campos and pampas <strong>grass</strong>lands <strong>of</strong> South America, but as in other areas <strong>of</strong> the world, the ancient and pre-<br />

European fire regimes are poorly understood. Darwin (1845 p. 114) reported that the plains from Bahía Blanca to Buenos Aires<br />

were commonly deliberately burnt, “chiefly for improving the pasture”: “it seems necessary to remove the superfluous<br />

49

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