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<strong>Underp<strong>in</strong>n<strong>in</strong>gs</strong> <strong>of</strong> <strong>fire</strong> <strong>management</strong> <strong>for</strong> <strong>biodiversity</strong> <strong>conservation</strong> <strong>in</strong> reserves<br />

Fire and adaptive <strong>management</strong><br />

Percent cover<br />

64<br />

In Figure 4.1, the plant species are arranged <strong>in</strong> order <strong>of</strong> cover, presumed to be proportional to<br />

biomass, all <strong>of</strong> which is assumed to be fuel <strong>in</strong> this grassland example. The curve represents very<br />

high dom<strong>in</strong>ance <strong>of</strong> one species and drastically lower cover classes <strong>for</strong> other species. In this grassland<br />

context, the most abundant species may be referred to as a ‘fuel species’ (Gill 1999a). At least one<br />

widespread grassland species <strong>in</strong> Australia – Themeda australis – is highly palatable (e.g. Allcock<br />

and Hik 2004) and a dom<strong>in</strong>ant fuel species; while at least one exotic dom<strong>in</strong>ant – Serrated Tussock<br />

(Nassella trichotoma) – is unpalatable (Lunt 2005 p. 24), but also a fuel species. The dom<strong>in</strong>ant grass<br />

species changes spatially, sometimes with<strong>in</strong> short distances.<br />

100<br />

10<br />

1<br />

0.1<br />

0.01<br />

0.001<br />

y = 72.406x -2.214<br />

R 2 = 0.9866<br />

1 7 13 19 25 31 37 43 49 55 61 67 73 79 85 91 97<br />

Species rank<br />

Figure 4.1 102 species <strong>of</strong> a montane grassland <strong>in</strong> Namadgi National Park, ACT, arranged <strong>in</strong> order <strong>of</strong> their overlapp<strong>in</strong>g cover<br />

values; 95 species have less than 1% cover (Graph courtesy <strong>of</strong> Dr R Godfrey, CSIRO, 2006). Note the logarithmic Y-axis.<br />

Relatively small rare herbs <strong>in</strong> the tail <strong>of</strong> a frequency distribution, such as that <strong>in</strong> Figure 4.1, <strong>in</strong> the<br />

herbivore context, may be most readily envisaged as locally rare. The dom<strong>in</strong>ant species, <strong>in</strong> the<br />

fuel context, may be regarded as hav<strong>in</strong>g ubiquitous occurrence. In a <strong>conservation</strong> context, at the<br />

landscape scale, species may persist because <strong>of</strong> heterogeneity <strong>of</strong> habitat. For example, niches <strong>for</strong><br />

herbs desired by graz<strong>in</strong>g animals may occur among unpalatable grasses or prickly shrubs or <strong>in</strong> rocky<br />

terra<strong>in</strong> where a herbivore’s <strong>for</strong>ag<strong>in</strong>g rewards are less pronounced. While this may be the case <strong>in</strong> some<br />

landscapes, Landsberg et al. (2002), work<strong>in</strong>g <strong>in</strong> north-west South Australia, found that selectively<br />

chosen and uncommon or short-lived species, ‘are more likely to decl<strong>in</strong>e everywhere’, not just near<br />

the more heavily grazed water po<strong>in</strong>ts.<br />

Graz<strong>in</strong>g regimes<br />

In this section, the concept <strong>of</strong> the graz<strong>in</strong>g regime is expla<strong>in</strong>ed. It is addressed at the level <strong>of</strong> a plantsized<br />

patch or po<strong>in</strong>t <strong>in</strong> the landscape – as opposed to an area e.g. paddock. This reflects the scale <strong>of</strong><br />

the animal’s immediate <strong>in</strong>fluence through herbivory and recognises that some plants or plant parts are<br />

palatable while others are not.<br />

The components <strong>of</strong> a graz<strong>in</strong>g regime are:<br />

• Type <strong>of</strong> animal<br />

• Intensity <strong>of</strong> herbivory (e.g. amount or proportion <strong>of</strong> plant removal on each graz<strong>in</strong>g occasion)<br />

• Interval between disturbances (e.g. time between consum<strong>in</strong>g the shoots <strong>of</strong> the same grassy plant)<br />

• Seasonality (<strong>of</strong> shoot removal).<br />

The parallel with <strong>fire</strong> regimes may be apparent. Interactions between graz<strong>in</strong>g regimes and the<br />

environment <strong>in</strong> which the animals live are to be expected. The graz<strong>in</strong>g-regime approach is different<br />

to that <strong>of</strong> traditional farm experiments, where <strong>in</strong>tensity <strong>of</strong> graz<strong>in</strong>g is given as a ‘stock<strong>in</strong>g rate’ <strong>for</strong> a<br />

paddock as a whole, rather than <strong>for</strong> a po<strong>in</strong>t with<strong>in</strong> a paddock (as above). Po<strong>in</strong>t approaches allow <strong>for</strong>

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