202 research outputs found

    Spatial autocorrelation and the selection of simultaneous autoregressive models

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    ABSTRACT Aim Spatial autocorrelation is a frequent phenomenon in ecological data and can affect estimates of model coefficients and inference from statistical models. Here, we test the performance of three different simultaneous autoregressive (SAR) model types (spatial error = SAR err , lagged = SAR lag and mixed = SAR mix ) and common ordinary least squares (OLS) regression when accounting for spatial autocorrelation in species distribution data using four artificial data sets with known (but different) spatial autocorrelation structures. Methods We evaluate the performance of SAR models by examining spatial patterns in model residuals (with correlograms and residual maps), by comparing model parameter estimates with true values, and by assessing their type I error control with calibration curves. We calculate a total of 3240 SAR models and illustrate how the best models [in terms of minimum residual spatial autocorrelation (minRSA), maximum model fit ( R 2 ), or Akaike information criterion (AIC)] can be identified using model selection procedures. Results Our study shows that the performance of SAR models depends on model specification (i.e. model type, neighbourhood distance, coding styles of spatial weights matrices) and on the kind of spatial autocorrelation present. SAR model parameter estimates might not be more precise than those from OLS regressions in all cases. SAR err models were the most reliable SAR models and performed well in all cases (independent of the kind of spatial autocorrelation induced and whether models were selected by minRSA, R 2 or AIC), whereas OLS, SAR lag and SAR mix models showed weak type I error control and/or unpredictable biases in parameter estimates. Main conclusions SAR err models are recommended for use when dealing with spatially autocorrelated species distribution data. SAR lag and SAR mix might not always give better estimates of model coefficients than OLS, and can thus generate bias. Other spatial modelling techniques should be assessed comprehensively to test their predictive performance and accuracy for biogeographical and macroecological research

    Mammal predator and prey species richness are strongly linked at macroscales

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    Predator-prey interactions play an important role for species composition and community dynamics at local scales, but their importance in shaping large-scale gradients of species richness remains unexplored. Here, we use global range maps, structural equation models (SEM), and comprehensive databases of dietary preferences and body masses of all terrestrial, non-volant mammals worldwide, to test whether (1) prey bottom-up or predator top-down relationships are important drivers of broad-scale species richness gradients once the environment and human influence have been accounted for, (2) predator-prey richness associations vary among biogeographic regions, and (3) body size influences large-scale covariation between predators and prey. SEMs including only productivity, climate, and human factors explained a high proportion of variance in prey richness (R2 = 0.56) but considerably less in predator richness (R2 = 0.13). Adding predator-to-prey or prey-topredator paths strongly increased the explained variance in both cases (prey R2 = 0.79, predator R2 = 0.57), suggesting that predator-prey interactions play an important role in driving global diversity gradients. Prey bottom-up effects prevailed over productivity, climate, and human influence to explain predator richness, whereas productivity and climate were more important than predator top-down effects for explaining prey richness, although predator top-down effects were still significant. Global predator-prey associations were not reproduced in all regions, indicating that distinct paleoclimate and evolutionary histories (Africa and Australia) may alter species interactions across trophic levels. Stronger crosstrophic- level associations were recorded within categories of similar body size (e.g., large prey to large predators) than between them (e.g., large prey to small predators), suggesting that mass-related energetic and physiological constraints influence broad-scale richness links, especially for large-bodied mammals. Overall, our results support the idea that trophic interactions can be important drivers of large-scale species richness gradients in combination with environmental effects. © 2013 by the Ecological Society of America

    Minimum Information Standards for Essential Biodiversity Variables

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    Minimum Information Standards (MIS) are sets of specifications for describing datasets that aim to standardize data reporting and to maximize its discoverability and interoperability. While MIS have greatly contributed to enhance the distribution and reuse of datasets in the biological and biomedical sciences, their adoption in ecology and biodiversity sciences is still incipient. Here we present a community effort to generate minimum standards for Essential Biodiversity Variables (EBVs). The operationalization of EBVs require integrating heterogeneous datasets of disparate origin and, often, to combine information from different geographic areas and time periods. Furthermore, developing policy-relevant indicators from EBVs requires an additional level of integration between datasets that inform on different facets of biodiversity, e.g. at levels from species to ecosystems. MIS for Essential Biodiversity Variables is founded in the description of the EBV-data cube as the unifying framework to deliver interoperable biodiversity observations. They summarize aspects of the spatial and temporal domains of the datasets, as well as uncertainty and bias reporting. MIS also incorporate the GEOSS proposed principles for data management. Finally, a metadata publishing toolkit will be developed in order to ensure that EBVs are discoverable and used under the auspices of GEO BON

    Towards global data products of Essential Biodiversity Variables on species traits

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    Essential Biodiversity Variables (EBVs) allow observation and reporting of global biodiversity change, but a detailed framework for the empirical derivation of specific EBVs has yet to be developed. Here, we re-examine and refine the previous candidate set of species traits EBVs and show how traits related to phenology, morphology, reproduction, physiology and movement can contribute to EBV operationalization. The selected EBVs express intra-specific trait variation and allow monitoring of how organisms respond to global change. We evaluate the societal relevance of species traits EBVs for policy targets and demonstrate how open, interoperable and machine-readable trait data enable the building of EBV data products. We outline collection methods, meta(data) standardization, reproducible workflows, semantic tools and licence requirements for producing species traits EBVs. An operationalization is critical for assessing progress towards biodiversity conservation and sustainable development goals and has wide implications for data-intensive science in ecology, biogeography, conservation and Earth observation

    Downsizing of animal communities triggers stronger functional than structural decay in seed-dispersal networks

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    Downsizing of animal communities due to defaunation is prevalent in many ecosystems. Yet, we know little about its consequences for ecosystem functions such as seed dispersal. Here, we use eight seed-dispersal networks sampled across the Andes and simulate how downsizing of avian frugivores impacts structural network robustness and seed dispersal. We use a trait-based modeling framework to quantify the consequences of downsizing—relative to random extinctions—for the number of interactions and secondary plant extinctions (as measures of structural robustness) and for long-distance seed dispersal (as a measure of ecosystem function). We find that downsizing leads to stronger functional than structural losses. For instance, 10% size-structured loss of bird species results in almost 40% decline of long-distance seed dispersal, but in less than 10% of structural loss. Our simulations reveal that measures of the structural robustness of ecological networks underestimate the consequences of animal extinction and downsizing for ecosystem functioning.Fil: Donoso, Isabel. Senckenberg Biodiversity and Climate Research Centre; AlemaniaFil: Sorensen, Marjorie C.. Senckenberg Biodiversity and Climate Research Centre; Alemania. University of Guelph; Canadá. Goethe Universitat Frankfurt; AlemaniaFil: Blendinger, Pedro Gerardo. Universidad Nacional de Tucumán. Instituto de Ecología Regional. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Ecología Regional; ArgentinaFil: Kissling, W. Daniel. University of Amsterdam; Países BajosFil: Neuschulz, Eike Lena. Senckenberg Biodiversity and Climate Research Centre; AlemaniaFil: Mueller, Thomas. Senckenberg Biodiversity and Climate Research Centre; AlemaniaFil: Schleuning, Matthias. Senckenberg Biodiversity and Climate Research Centre; Alemani

    To adapt or go extinct? The fate of megafaunal palm fruits under past global change

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    Past global change may have forced animal-dispersed plants with megafaunal fruits to adapt or go extinct, but these processes have remained unexplored at broad spatio-temporal scales. Here, we combine phylogenetic, distributional and fruit size data for more than 2500 palm (Arecaceae) species in a time-slice diversification analysis to quantify how extinction and adaptation have changed over deep time. Our results indicate that extinction rates of palms with megafaunal fruits have increased in the New World since the onset of the Quaternary (2.6 million years ago). In contrast, Old World palms show a Quaternary increase in transition rates towards evolving small fruits from megafaunal fruits. We suggest that Quaternary climate oscillations and concurrent habitat fragmentation and defaunation of megafaunal frugivores in the New World have reduced seed dispersal distances and geographical ranges of palms with megafaunal fruits, resulting in their extinction. The increasing adaptation to smaller fruits in the Old World could reflect selection for seed dispersal by ocean-crossing frugivores (e.g. medium-sized birds and bats) to colonize Indo-Pacific islands against a background of Quaternary sea-level fluctuations. Our macro-evolutionary results suggest that megafaunal fruits are increasingly being lost from tropical ecosystems, either due to extinctions or by adapting to smaller fruit sizes.</p

    Global patterns and drivers of phylogenetic structure in island floras

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    Islands are ideal for investigating processes that shape species assemblages because they are isolated &nbsp;and have discrete boundaries. Quantifying phylogenetic assemblage structure allows inferences in-situ speciation. Here, we link phylogenetic assemblage structure to island characteristics across 393 islands worldwide &nbsp;and 37,041 vascular plant species (representing angiosperms overall, palms and ferns). Physical and &nbsp;bioclimatic factors, especially those impeding colonization and promoting speciation, explained &nbsp;more &nbsp;variation &nbsp;in &nbsp;phylogenetic &nbsp;structure &nbsp;of &nbsp;angiosperms &nbsp;overall &nbsp;(49%) &nbsp;and &nbsp;palms &nbsp;(52%) &nbsp;than &nbsp;of &nbsp;ferns consistent with their dispersal- and speciation-related traits and climatic adaptations. Phylogenetic &nbsp;diversity was negatively related to isolation for palms, but unexpectedly it was positively related large-seeded, animal-dispersed palm family whereas colonization from biogeographically distinct in-situ among taxonomic groups on islands, which sheds light on the origin of insular plant diversity.</p

    The role of deterministic succession during forest development within a southern African savanna

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    Woody encroachment can lead to a switch from open savannas to dense woodlands or forests. This has implications for both the composition of ecological communities and the provision of ecosystem services such as nutrient cycling and grazing capacity. The patterns and underlying drivers responsible for woody encroachment are not fully understood. Here, we investigate the underlying determinants of bush clump formation (a form of encroachment) in a South African savanna and explore whether bush clump succession is driven by deterministic (i.e., predictable changes in species composition) or stochastic (i.e., random) processes. Specifically, we test (1) whether the similarity in species composition of saplings and trees differs among small and large clumps, (2) which environmental factors are driving succession, and (3) whether forest specialization of tree and sapling species within bush clumps increases with the successional gradient. Similarity in species composition between saplings in small clumps and trees in large clumps was higher than similarity between trees in small clumps and trees in large clumps. Furthermore, temperature, soil moisture, relative humidity, and light intensity were related to changes in species composition along the successional gradient. As expected, forest specialization of trees increased with increasing clump area indicating that late‐successional bush clumps have more forest‐type species. The directional changes of species found along the successional gradient suggest a deterministic process of succession driven by changes in local environmental conditions during clump formation.The Universiteit van Amsterdam (UvA) and the National Research Foundation.http://wileyonlinelibrary.com/journal/btp2022-03-10hj2021Forestry and Agricultural Biotechnology Institute (FABI)Plant Production and Soil Scienc

    Research infrastructure challenges in preparing essential biodiversity variables data products for alien invasive species

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    Essential Biodiversity Variables (EBV) are information products for assessing biodiversity change. Species populations EBVs are one class of EBVs that can be used to monitor the spread of invasive species. However, systematic, reliable, repeatable procedures to process primary data into EBVs do not yet exist, and environmental research infrastructures still must improve their capabilities to deliver EBV data products. Here, we tested the ability of two mature biodiversity data infrastructures, the Global Biodiversity Information Facility and the Atlas of Living Australia to cooperatively produce EBV data products for three alien invasive species. We detailed workflow steps to discover, filter, retrieve and prepare the primary data before evaluating species’ distributional changes. The two data infrastructures were able to execute several workflow steps, but external tools, third-party sources and expert judgement were required, and a repeatable workflow was difficult to establish. Nevertheless, the resulting data products revealed strong range expansions for the invasive species, demonstrating the policy-relevant information about global environmental change that can be provided by EBV data products. Our results show that more coordination between infrastructure providers is needed to efficiently produce EBV-ready data products for invasion monitoring in a repeatable fashion. Addressing these issues will allow improved tracking of invasive species range dynamics and hence monitoring of ongoing global biodiversity change
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