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Linking Restoration and Ecological Succession (Springer ... - Inecol

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Chapter 3 Aboveground–Belowground Linkages, Ecosystem Development, <strong>and</strong> Ecosystem <strong>Restoration</strong> 57<br />

conservation perspective, <strong>and</strong> this issue has generated significant recent debate<br />

(Niklasson <strong>and</strong> Granström 2004). However, in Sc<strong>and</strong>inavian forests, prescribed<br />

burning has been increasingly introduced in forests that are managed for production,<br />

mainly because of their perceived benefits for nutrient cycling <strong>and</strong><br />

long-term forest st<strong>and</strong> productivity (Niklasson <strong>and</strong> Granström 2004, Nilsson<br />

<strong>and</strong> Wardle 2005). The studies described above for forested isl<strong>and</strong>s, as well<br />

as other related studies (reviewed by Nilsson <strong>and</strong> Wardle 2005) provide evidence<br />

that restoration of natural fire regimes (or implementation of prescribed<br />

burning) should serve to reverse ecosystem retrogression, promote rates of soil<br />

processes, <strong>and</strong> enhance forest productivity, at least in the order of decades. At a<br />

more globally relevant level, these forests are also important global carbon sinks<br />

or sources <strong>and</strong> restoration through introduction of a fire regime is likely to exert<br />

major effects on the amounts of carbon these forests store or release as CO2.<br />

Most of the forests in Sc<strong>and</strong>inavia are under some form of management <strong>and</strong><br />

are utilized to varying degrees for timber <strong>and</strong> pulp production. Management for<br />

conservation benefits <strong>and</strong> for production forestry are not necessarily incompatible,<br />

<strong>and</strong> restoration of appropriate fire regimes may be useful for maximizing<br />

goals associated with each of these activities.<br />

3.5 Belowground Impacts of Invasive Nonnative Plants<br />

Invasive nonnative plants are widely perceived to have major, negative impacts<br />

in ecosystems (Pimentel et al. 2000, Mack et al. 2000, Myers <strong>and</strong> Bazley 2003),<br />

<strong>and</strong> the nature of spread <strong>and</strong> increased abundance of invasive plants has been<br />

documented for several species <strong>and</strong> systems. The relationships of these invaders<br />

with aboveground properties such as NPP <strong>and</strong> native vegetation diversity have<br />

been frequently studied (Daehler 2003, Ehrenfeld 2003, Levine et al. 2003),<br />

<strong>and</strong> it is recognized that these relationships vary strongly among both systems<br />

<strong>and</strong> species (see Hierro et al. 2005, Yurkonis et al. 2005; see Chapter 6). In<br />

contrast, impacts on belowground properties, processes, <strong>and</strong> communities are<br />

less well understood, although these may have profound implications for both<br />

successional processes <strong>and</strong> restoration efforts (Suding et al. 2004, Wolfe <strong>and</strong><br />

Klironomos 2005, Young et al. 2005).<br />

The best-documented belowground consequences of invasive plants are increases<br />

in soil nutrient fluxes, particularly of N. This is because many of the<br />

most widespread <strong>and</strong> successful invaders are plants associated with N-fixing<br />

symbionts, for example, those in the genera Acacia, Cytisus, Lupinus, Melilotus,<br />

Ulex, <strong>and</strong> Trifolium (Ehrenfeld 2003, Levine et al. 2003). These N-fixing plants<br />

should have important belowground impacts in N-limited ecosystems, as was<br />

first demonstrated by Vitousek et al. (1987) who found that the woody N-fixing<br />

invader Myrica faya increased N availability in Hawaiian ecosystems above that<br />

in native-dominated systems. Not surprisingly, many subsequent studies on the<br />

impacts of N-fixing invaders have found elevated levels of N availability across<br />

a range of species <strong>and</strong> systems (reviewed by Ehrenfeld 2003, Levine et al.<br />

2003). A common assumption across these studies is that invading N-fixing<br />

plants are better able to garner N than their native counterparts, presumably due<br />

to their higher growth rates or greater per capita impacts on nutrient inputs into a<br />

system (although these possibilities have been little explored to date). A recent<br />

study by Weir et al. (2004) showed that different N-fixing bacterial mutualists

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