144 research outputs found

    Complementary effects of species abundances and ecological neighborhood on the occurrence of fruit-frugivore interactions

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    Species interactions are traditionally seen as the outcome of both ecological and evolutionary mechanisms. Among them, the two most frequently studied are the neutral role of species abundances in determining encounter probability and the deterministic role of species identity (traits and evolutionary history) in determining the compatibility of interacting species. Nevertheless, the occurrence of pairwise interactions also depends on the spatio-temporal context imposed by the ecological neighborhood (i.e., the indirect effect of other local species sharing traits and interaction potential with the focal ones). Although a few studies have begun to examine neighborhood effects on community interactions, these have not incorporated neighborhood structure as a complementary driver of pairwise interactions within an integrative approach. Here we describe the spatial structure of pairwise interactions between three fleshy-fruited tree species and six frugivorous thrush species within the same locality of the Cantabrian Range (Iberian Peninsula). Using a spatio-temporally fine-grained dataset sampled during 3 years, we aimed to detect spatial patterns of interactions and to evaluate their concordance across years. We also evaluated the simultaneous roles played by species abundance, species identity and the ecological neighborhood in determining the pairwise interaction frequencies based on fruit removal. Our results showed that the abundances of fruit and bird species involved in plant-frugivore interactions, and the spatial patterns of these interactions, varied among years, and this was mainly due to different fruiting landscapes responding to masting events of distinct plant species. Despite high interannual differences in species abundances and pairwise interaction frequencies, the main mechanisms underpinning the occurrence of pairwise interactions remained constant. Most of the variability in pairwise interactions was always explained by interacting fruit and bird species' abundances. Ecological neighborhood, characterized as the net quantity of forest cover, heterospecific fruit crops, and heterospecific bird abundances in the immediate surroundings, also affected pairwise interaction frequency through its indirect effects on the abundance of interacting bird species. Our results highlight the prevalence of neutral forces in highly generalized plant-frugivore assemblages as well as the influence of indirect interactions (competition and/or facilitation with other local species) as another important driver to consider when predicting pairwise interactions

    Structural efficiency of percolation landscapes in flow networks

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    Complex networks characterized by global transport processes rely on the presence of directed paths from input to output nodes and edges, which organize in characteristic linked components. The analysis of such network-spanning structures in the framework of percolation theory, and in particular the key role of edge interfaces bridging the communication between core and periphery, allow us to shed light on the structural properties of real and theoretical flow networks, and to define criteria and quantities to characterize their efficiency at the interplay between structure and functionality. In particular, it is possible to assess that an optimal flow network should look like a "hairy ball", so to minimize bottleneck effects and the sensitivity to failures. Moreover, the thorough analysis of two real networks, the Internet customer-provider set of relationships at the autonomous system level and the nervous system of the worm Caenorhabditis elegans --that have been shaped by very different dynamics and in very different time-scales--, reveals that whereas biological evolution has selected a structure close to the optimal layout, market competition does not necessarily tend toward the most customer efficient architecture.Comment: 8 pages, 5 figure

    Potential climatic transitions with profound impact on Europe

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    We discuss potential transitions of six climatic subsystems with large-scale impact on Europe, sometimes denoted as tipping elements. These are the ice sheets on Greenland and West Antarctica, the Atlantic thermohaline circulation, Arctic sea ice, Alpine glaciers and northern hemisphere stratospheric ozone. Each system is represented by co-authors actively publishing in the corresponding field. For each subsystem we summarize the mechanism of a potential transition in a warmer climate along with its impact on Europe and assess the likelihood for such a transition based on published scientific literature. As a summary, the ‘tipping’ potential for each system is provided as a function of global mean temperature increase which required some subjective interpretation of scientific facts by the authors and should be considered as a snapshot of our current understanding. <br/

    Environmental context, parameter sensitivity and structural sensitivity impact predictions of annual-plant coexistence

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    Predicting the outcome of interactions between species is central to our current understanding of diversity maintenance. However, we have limited information about the robustness of many model-based predictions of species coexistence. This limitation is partly because several sources of uncertainty are often ignored when making predictions. Here, we introduce a framework to simultaneously explore how different mathematical models, different environmental contexts, and parameter uncertainty impact the probability of predicting species coexistence. Using a set of pairwise competition experiments on annual plants, we provide direct evidence that subtle differences between models lead to contrasting predictions of both coexistence and competitive exclusion. We also show that the effects of environmental context dependency and parameter uncertainty on predictions of species coexistence are not independent of the model used to describe population dynamics. Our work suggests that predictions of species coexistence and extrapolations thereof may be particularly vulnerable to these underappreciated founts of uncertainty.fals

    A comparison of missing data methods for hypothesis tests of the treatment effect in substance abuse clinical trials: a Monte-Carlo simulation study

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    <p>Abstract</p> <p>Background</p> <p>Missing data due to attrition are rampant in substance abuse clinical trials. However, missing data are often ignored in the presentation of substance abuse clinical trials. This paper demonstrates missing data methods which may be used for hypothesis testing.</p> <p>Methods</p> <p>Methods involving stratifying and weighting individuals based on missing data pattern are shown to produce tests that are robust to missing data mechanisms in terms of Type I error and power. In this article, we describe several methods of combining data that may be used for testing hypotheses of the treatment effect. Furthermore, illustrations of each test's Type I error and power under different missing data percentages and mechanisms are quantified using a Monte-Carlo simulation study.</p> <p>Results</p> <p>Type I error rates were similar for each method, while powers depended on missing data assumptions. Specifically, power was greatest for the weighted, compared to un-weighted methods, especially for greater missing data percentages.</p> <p>Conclusion</p> <p>Results of this study as well as extant literature demonstrate the need for standards of design and analysis specific to substance abuse clinical trials. Given the known substantial attrition rates and concern for the missing data mechanism in substance abuse clinical trials, investigators need to incorporate missing data methods a priori. That is, missing data methods should be specified at the outset of the study and not after the data have been collected.</p
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