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166<br />

M. Scherer-Lorenzen, H. Olde Venterink, and H. Buschmann<br />

decomposition rates, since legumes often have relatively high N concentrations,<br />

which might stimulate litter decomposition rates (Ehrenfeld 2003).<br />

10.2.3 Major Invasive Nitrogen-Fixing Species<br />

Also other researchers came to the conclusion that there are hardly any data<br />

available about the N input into the ecosystem by N 2 fixation of exotic invading<br />

species. One reason for this may be the lack of precise methods for quantifying<br />

N 2 -fixation rates. Nevertheless, there are some data available for some<br />

of these species when growing in their native range or in plantations. The N<br />

input values from these studies might give an indication of the potential<br />

importance of N 2 fixation when these species are invading. We note that rates<br />

in plantations could be higher than those in natural areas because of more<br />

optimal growth conditions in the former. Below, we will shortly present examples<br />

of some important invading N 2 -fixing species, and their possible influence<br />

on N cycling and related ecosystem processes.<br />

Myrica faya. As mentioned above, Myrica faya increased annual N input in<br />

young volcanic soils about fourfold. This additional nitrogen cycles rapidly<br />

within the system, increases nitrogen availability, enhances plant productivity,<br />

and alters community structure by differentially affecting survival and<br />

growth (Vitousek and Walker 1989; Walker and Vitousek 1991). It is interesting<br />

to note that these volcanic soils are poor in nitrogen, rich in phosphorus,<br />

and have scarce vegetation. Hence, these young soils are nitrogen-limited. M.<br />

faya does not invade on older, P-limited soils (Vitousek 2004).<br />

Albizia falcataria (=Falcataria moluccana or Paraserianthes falcataria).<br />

There are several studies investigating the influence of N 2 -fixing Albizia falcataria<br />

and non-N 2 -fixing Eucalyptus saligna on soil properties and productivity<br />

of tree plantations (e.g., Binkley 1997; Garcia-Montiel and Binkley 1998;<br />

Binkley et al. 2003). Both species were introduced on Hawaii. Compared with<br />

E. saligna monocultures, mixed stands of E. saligna and A. falcataria may produce<br />

more biomass, contain larger aboveground nutrient pools, and cycle<br />

more nutrients through litterfall. A. falcataria can increase N pools in tropical<br />

soils with N limitation almost threefold. There are also indications that A. falcataria<br />

is able to acquire more P from the soil than is the case for E. saligna,<br />

leading to reduced soil P pools. As the effects of A. falcataria have been measured<br />

only in plantations, it is unknown whether it also causes N enrichment<br />

in natural ecosystems. This seems a very relevant question, since A. falcataria<br />

is an important invasive tree in some tropical areas.<br />

Acacia spp. Invasive Acacia species have been intensively investigated in<br />

South African ecosystems. The results of these studies are unequivocal and

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