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Developments of future scenarios of Antarctic ecosystems are still in their infancy, whilst predictions of the physical environment are recognized as being of global relevance and corresponding models are under continuous development. However, in the context of environmental change simulations of the future of the Antarctic biosphere are increasingly demanded by decision makers and the public, and are of fundamental scientific interest. This paper briefly reviews existing predictive models applied to Antarctic ecosystems before providing a conceptual framework for the further development of spatially and temporally explicit ecosystem models. The concept suggests how to improve approaches to relating species' habitat description to the physical environment, for which a case study on sea urchins is presented. In addition, the concept integrates existing and new ideas to consider dynamic components, particularly information on the natural history of key species, from physiological experiments and biomolecular analyses. Thereby, we identify and critically discuss gaps in knowledge and methodological limitations. These refer to process understanding of biological complexity, the need for high spatial resolution oceanographic data from the entire water column, and the use of data from biomolecular analyses in support of such ecological approaches. Our goal is to motivate the research community to contribute data and knowledge to a holistic, Antarctic-specific, macroecological framework. Such a framework will facilitate the integration of theoretical and empirical work in Antarctica, improving our mechanistic understanding of this globally influential ecoregion, and supporting actions to secure this biodiversity hotspot and its ecosystem services.
Facilitation (positive interaction) has received increasing attention in plant ecology over the last decade. Just as for competition, distinguishing different modes of facilitation (mutualistic, commensal or even antagonistic) may be crucial. We therefore introduce the new concept of symmetric versus asymmetric facilitation and present a generic individual-based zone-of-influence model. The model simultaneously implements different modes of both facilitation and competition among individual plants via their overlapping zone of influence. Because we consider facilitation modes as a continuum related to environmental context, we integrated this concept with the stress-gradient hypothesis (SGH) by exploring differences in spatial pattern formation in self-thinning plants along a stress gradient in our model. The interplay among modes of interaction creates distinctly varied spatial patterns along stress gradients. When competition was symmetric, symmetric facilitation (mutualism) consistently led to plant aggregation along stress gradients. However, asymmetric facilitation (commensalism) produces plant aggregation only under more benign conditions but tends to intensify local competition and spatial segregation when conditions are harsh. When competition was completely asymmetric, different modes of facilitation contributed little to spatial aggregation. Symmetric facilitation significantly increased survival at the severe end of the stress gradient, which supports the claim of the SGH that facilitation should have generally positive net effects on plants under high stress levels. Asymmetric facilitation, however, was found to increase survival only under intermediate stress conditions, which contradicts the current predictions of the SGH. Synthesis. Our modelling study demonstrates that the interplay between modes of facilitation and competition affects different aspects of plant populations and communities, implying context-dependent outcomes and consequences. The explicit consideration of the modes and mechanisms of interactions (both facilitation and competition) and the nature of stress factors will help to extend the framework of the SGH and foster research on facilitation in plant ecology.
Empirical species distribution models (SDMs) constitute often the tool of choice for the assessment of rapid climate change effects on species vulnerability. Conclusions regarding extinction risks might be misleading, however, because SDMs do not explicitly incorporate dispersal or other demographic processes. Here, we supplement SDMs with a dynamic population model 1) to predict climate-induced range dynamics for black grouse in Switzerland, 2) to compare direct and indirect measures of extinction risks, and 3) to quantify uncertainty in predictions as well as the sources of that uncertainty. To this end, we linked models of habitat suitability to a spatially explicit, individual-based model. In an extensive sensitivity analysis, we quantified uncertainty in various model outputs introduced by different SDM algorithms, by different climate scenarios and by demographic model parameters. Potentially suitable habitats were predicted to shift uphill and eastwards. By the end of the 21st century, abrupt habitat losses were predicted in the western Prealps for some climate scenarios. In contrast, population size and occupied area were primarily controlled by currently negative population growth and gradually declined from the beginning of the century across all climate scenarios and SDM algorithms. However, predictions of population dynamic features were highly variable across simulations. Results indicate that inferring extinction probabilities simply from the quantity of suitable habitat may underestimate extinction risks because this may ignore important interactions between life history traits and available habitat. Also, in dynamic range predictions uncertainty in SDM algorithms and climate scenarios can become secondary to uncertainty in dynamic model components. Our study emphasises the need for principal evaluation tools like sensitivity analysis in order to assess uncertainty and robustness in dynamic range predictions. A more direct benefit of such robustness analysis is an improved mechanistic understanding of dynamic species responses to climate change.