Linking Specialisation and Stability of Plant ... - OPUS Würzburg
Linking Specialisation and Stability of Plant ... - OPUS Würzburg
Linking Specialisation and Stability of Plant ... - OPUS Würzburg
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4.5 discussion 81<br />
termine the range <strong>of</strong> starting conditions <strong>and</strong> the appropriate<br />
time scale.<br />
Although the model used in this study contains a fair amount<br />
<strong>of</strong> mechanistic detail, it still makes a number <strong>of</strong> simplifying assumptions<br />
that may impact the results <strong>of</strong> our analyses. In the<br />
following, we discuss potential caveats <strong>and</strong> limitations <strong>of</strong> our<br />
modelling approach, <strong>and</strong> suggest directions for future research.<br />
First, the results presented in this paper to some degree depend<br />
on the choice <strong>of</strong> parameter values for numerical simulations,<br />
specifically on the assumption <strong>of</strong> an equal number <strong>of</strong> plant <strong>and</strong><br />
animal individuals in the system at equilibrium. Choosing a<br />
lower animal-plant ratio results in a narrower range <strong>of</strong> specialisation<br />
<strong>and</strong> niche overlap values allowing qualitative stability <strong>of</strong><br />
the coexistence equilibrium, while a higher animal-plant ratio<br />
extends that region (see Benadi et al., 2012b). However, a different<br />
animal-plant ratio does not qualitatively affect the patterns<br />
presented in this study for the region allowing stable coexistence.<br />
As discussed in Benadi et al. (2012b), the few available<br />
empirical studies indicate that the amount <strong>of</strong> floral resources<br />
needed to sustain one animal varies widely, but at least for pollination<br />
mutualisms it seems that the ratio <strong>of</strong> animal to plant<br />
individuals is usually below one. On related terms, the choice<br />
<strong>of</strong> equal competition coefficients for both plant species, constant<br />
sums <strong>of</strong> trait matching values for all mutualistic interactions<br />
<strong>and</strong> equal values for all other parameters in this study<br />
was made in order to concentrate on the effects <strong>of</strong> communitywide<br />
specialisation. Since real mutualistic systems always deviate<br />
from the perfect symmetry assumed in this study, future<br />
work should explore the consequences <strong>of</strong> asymmetric interaction<br />
strengths <strong>and</strong> demographic parameters. For example, it<br />
would be interesting to study the consequences <strong>of</strong> a trade-<strong>of</strong>f<br />
in plant competitive ability with respect to abiotic resources<br />
<strong>and</strong> attractiveness towards pollinators. Furthermore, future research<br />
should target larger mutualistic communities containing<br />
a mixture <strong>of</strong> various degrees <strong>of</strong> specialisation, <strong>and</strong> elucidate the<br />
effect <strong>of</strong> different distributions <strong>of</strong> specialisation levels on community<br />
stability. Some attempts in this direction have already<br />
been made (see e.g. Okuyama & Holl<strong>and</strong>, 2008; Bastolla et al.,<br />
2009), but much remains to be understood.<br />
The current study is to some extent a theoretical exercise<br />
whose predictions are difficult to test in the field. Its main<br />
result, the finding that no single relationship between specialisation<br />
<strong>and</strong> stability <strong>of</strong> mutualistic systems exists, is bad news<br />
for conservationists <strong>and</strong> managers in search <strong>of</strong> rules <strong>of</strong> thumb<br />
for assessing the fragility <strong>of</strong> ecological systems. In order to