AbstractSpecies' interactions are shaped by their traits. Thus, we expect traits-in particular, trait (dis)similarity-to play a central role in determining whether a particular set of species coexists. Traits are, in turn, the outcome of an eco-evolutionary process summarized by a phylogenetic tree.
View Article and Find Full Text PDFEcological assembly is a fundamental and yet poorly understood process. Three main obstacles hinder the development of a theory of assembly, and when these issues are sidestepped by making strong assumptions, one can build an assembly graph in which nodes are ecological communities and edges are invasions shifting their composition. The graph can then be analysed directly, without the need to consider dynamics.
View Article and Find Full Text PDFNetwork data sets are often constructed by some kind of thresholding procedure. The resulting networks frequently possess properties such as heavy-tailed degree distributions, clustering, large connected components, and short average shortest path lengths. These properties are considered typical of complex networks and appear in many contexts, prompting consideration of their universality.
View Article and Find Full Text PDFIntraspecific variation is at the core of evolutionary theory, and yet, from an ecological perspective, we have few robust expectations for how this variation should affect the dynamics of large communities. Here, by adapting an approach from evolutionary game theory, we show that the incorporation of phenotypic variability into competitive networks dramatically alters the dynamics across ecological timescales, stabilising the systems and buffering the communities against demographic perturbations. The beneficial effects of phenotypic variability are strongest when there are substantial differences among phenotypes and when phenotypes are inherited with moderately high fidelity; yet even low levels of variation lead to significant increases in diversity, stability, and robustness.
View Article and Find Full Text PDFCoexistence in ecological communities is governed largely by the nature and intensity of species interactions. Countless studies have proposed methods to infer these interactions from empirical data, yet models parameterised using such data often fail to recover observed coexistence patterns. Here, we propose a method to reconcile empirical parameterisations of community dynamics with species-abundance data, ensuring that the predicted equilibrium is consistent with the observed abundance distribution.
View Article and Find Full Text PDFRich ecosystems harbour thousands of species interacting in tangled networks encompassing predation, mutualism and competition. Such widespread biodiversity is puzzling, because in ecological models it is exceedingly improbable for large communities to stably coexist. One aspect rarely considered in these models, however, is that coexisting species in natural communities are a selected portion of a much larger pool, which has been pruned by population dynamics.
View Article and Find Full Text PDFEcological networks that exhibit stable dynamics should theoretically persist longer than those that fluctuate wildly. Thus, network structures which are over-represented in natural systems are often hypothesised to be either a cause or consequence of ecological stability. Rarely considered, however, is that these network structures can also be by-products of the processes that determine how new species attempt to join the community.
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