52 research outputs found

    Agricultural land-use and biological conservation

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    Land use change is a main driver of biodiversity erosion, especially in agricultural landscapes. Incentive-based land-use policies aim at influence land-use pattern, and are usually evaluated with habitat suitability scores, without accounting explicitly for the ecology of the studied population. In this paper, we propose a methodology to define and evaluate agricultural land-use policies with respect to their ecological outcomes directly. We use an ecological-economic model to link the regional abundance of a bird species to the economic context. Policies based on such ecological economics approaches appear to be more efficient than that based on landscape evaluation, from both economic and ecological viewpoints.Ecological-economic model, agriculture, land-use, landscape, conservation

    No sensitivity to functional forms in the strongly forced, continuous-time stochastic Rosenzweig-MacArthur model

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    The classic Rosenzweig-MacArthur predator-prey model has been shown to exhibit, like other coupled nonlinear ordinary differential equations (ODEs) from ecology, worrying sensitivity to model structure. This sensitivity manifests as markedly different community dynamics arising from saturating functional responses with nearly identical shapes but different mathematical expressions. Using a stochastic differential equation (SDE) version of the Rosenzweig-MacArthur model with the three functional responses considered by Fussman & Blasius (2005), I show that such sensitivity seems to be solely a property of ODEs or stochastic systems with weak noise. SDEs with strong environmental noise have by contrast very similar fluctuations patterns, irrespective of the mathematical formula used. Although eigenvalues of linearised predator-prey models have been used as an argument for structural sensitivity, they can also be an argument against structural sensitivity. While the sign of the eigenvalues' real part is sensitive to model structure, its magnitude and the presence of imaginary parts are not, which suggests noise-driven oscillations for a broad range of carrying capacities. I then discuss multiple other ways to evaluate structural sensitivity in a stochastic setting, for predator-prey or other ecological systems

    Effects of stage structure on coexistence: mixed benefits

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    The properties of competition models where all individuals are identical are relatively well-understood; however, juveniles and adults can experience or generate competition differently. We study here less well-known structured competition models in discrete time that allow multiple life history parameters to depend on adult or juvenile population densities. A numerical study with Ricker density-dependence suggested that when competition coefficients acting on juvenile survival and fertility reflect opposite competitive hierarchies, stage structure could foster coexistence. We revisit and expand those results. First, through a Beverton-Holt two-species juvenile-adult model, we confirm that these findings do not depend on the specifics of density-dependence or life cycles, and obtain analytical expressions explaining how this coexistence emerging from stage structure can occur. Second, we show using a community-level sensitivity analysis that such emergent coexistence is robust to perturbations of parameter values. Finally, we ask whether these results extend from two to many species, using simulations. We show that they do not, as coexistence emerging from stage structure is only seen for very similar life-history parameters. Such emergent coexistence is therefore not likely to be a key mechanism of coexistence in very diverse ecosystems, although it may contribute to explaining coexistence of certain pairs of intensely competing species

    Covariation between mean vole density and variability drives the numerical response of storks to vole prey

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    Hušek et al. (Popul Ecol 55:363–375, 2013) showed that the numerical response of storks to vole prey was stronger in regions where variability in vole density was higher. This finding is, at first sight, in contradiction with the predictions of life-history theory in stochastic environments. Since the stork productivity-vole density relationship is concave, theory predicts a negative association between the temporal variability in vole density and stork productivity. Here, we illustrate this negative effect of vole variability on stork productivity with a simple mathematical model relating expected stork productivity to vole dynamics. When comparing model simulations to the observed mean density and variability of thirteen Czech and Polish vole populations, we find that the observed positive effect of vole variability on stork numerical response is most likely due to an unusual positive correlation between mean and variability of vole density

    Survival rates of adult and juvenile gyrfalcons in Iceland: estimates and drivers

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    Knowledge of survival rates and their potential covariation with environmental drivers, for both adults and juveniles, is paramount to forecast the population dynamics of long-lived animals. Long-lived bird and mammal populations are indeed very sensitive to change in survival rates, especially that of adults. Here we report the first survival estimates for the Icelandic gyrfalcon (Falco rusticolus) obtained by capture-mark-recapture methods. We use a mark-recapture-recovery model combining live and dead encounters into a unified analysis, in a Bayesian framework. Annual survival was estimated at 0.83 for adults and 0.40 for juveniles. Positive effects of main prey density on juvenile survival (5% increase in survival from min to max density) were possible though not likely. Weather effects on juvenile survival were even less likely. The variability in observed lifespan suggests that adult birds could suffer from human-induced alteration of survival rates

    A Dynamic Occupancy Model for Interacting Species with Two Spatial Scales

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    Occupancy models have been extended to account for either multiple spatial scales or species interactions in a dynamic setting. However, as interacting species (e.g., predators and prey) often operate at different spatial scales, including nested spatial structure might be especially relevant to models of interacting species. Here we bridge these two model frameworks by developing a multi-scale, two-species occupancy model. The model is dynamic, i.e. it estimates initial occupancy, colonization and extinction probabilities—including probabilities conditional to the other species’ presence. With a simulation study, we demonstrate that the model is able to estimate most parameters without marked bias under low, medium and high average occupancy probabilities, as well as low, medium and high detection probabilities, with only a small bias for some parameters in low-detection scenarios. We further evaluate the model’s ability to deal with sparse field data by applying it to a multi-scale camera trapping dataset on a mustelid-rodent predator–prey system. Most parameters are estimated with low uncertainty (i.e. narrow posterior distributions). More broadly, our model framework creates opportunities to explicitly account for the spatial structure found in many spatially nested study designs, and to study interacting species that have contrasting movement ranges with camera traps.Supplementary materials accompanying this paper appear online.publishedVersio

    Within reach? Habitat availability as a function of individual mobility and spatial structuring

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    Organisms need access to particular habitats for their survival and reproduction. However, even if all necessary habitats are available within the broader environment, they may not all be easily reachable from the position of a single individual. Many species distribution models consider populations in environmental (or niche) space, hence overlooking this fundamental aspect of geographical accessibility. Here, we develop a formal way of thinking about habitat availability in environmental spaces by describing how limitations in accessibility can cause animals to experience a more limited or simply different mixture of habitats than those more broadly available. We develop an analytical framework for characterizing constrained habitat availability based on the statistical properties of movement and environmental autocorrelation. Using simulation experiments, we show that our general statistical representation of constrained availability is a good approximation of habitat availability for particular realizations of landscape-organism interactions. We present two applications of our approach, one to the statistical analysis of habitat preference (using step-selection functions to analyze harbor seal telemetry data) and a second that derives theoretical insights about population viability from knowledge of the underlying environment. Analytical expressions for habitat availability, such as those we develop here, can yield gains in analytical speed, biological realism, and conceptual generality by allowing us to formulate models that are habitat sensitive without needing to be spatially explicit

    Moving forward in circles: challenges and opportunities in modelling population cycles

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    Population cycling is a widespread phenomenon, observed across a multitude of taxa in both laboratory and natural conditions. Historically, the theory associated with population cycles was tightly linked to pairwise consumer–resource interactions and studied via deterministic models, but current empirical and theoretical research reveals a much richer basis for ecological cycles. Stochasticity and seasonality can modulate or create cyclic behaviour in non-intuitive ways, the high-dimensionality in ecological systems can profoundly influence cycling, and so can demographic structure and eco-evolutionary dynamics. An inclusive theory for population cycles, ranging from ecosystem-level to demographic modelling, grounded in observational or experimental data, is therefore necessary to better understand observed cyclical patterns. In turn, by gaining better insight into the drivers of population cycles, we can begin to understand the causes of cycle gain and loss, how biodiversity interacts with population cycling, and how to effectively manage wildly fluctuating populations, all of which are growing domains of ecological research
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