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1.
Protecting native biodiversity against alien invasive species requires powerful methods to anticipate these invasions and to protect native species assumed to be at risk. Here, we describe how species distribution models (SDMs) can be used to identify areas predicted as both suitable for rare native species and highly susceptible to invasion by alien species, at present and under future climate and land-use scenarios. To assess the condition and dynamics of such conflicts, we developed a combined predictive modelling (CPM) approach, which predicts species distributions by combining two SDMs fitted using subsets of predictors classified as acting at either regional or local scales. We illustrate the CPM approach for an alien invader and a rare species associated with similar habitats in northwest Portugal. Combined models predict a wider variety of potential species responses, providing more informative projections of species distributions and future dynamics than traditional, non-combined models. They also provide more informative insight regarding current and future rare-invasive conflict areas. For our studied species, conflict areas of highest conservation relevance are predicted to decrease over the next decade, supporting previous reports that some invasive species may contract their geographic range and impact due to climate change. More generally, our results highlight the more informative character of the combined approach to address practical issues in conservation and management programs, especially those aimed at mitigating the impact of invasive plants, land-use and climate changes in sensitive regions.  相似文献   

2.
Many species have already shifted their distributions in response to recent climate change. Here, we aimed at predicting the future breeding distributions of European birds under climate, land‐use, and dispersal scenarios. We predicted current and future distributions of 409 species within an ensemble forecast framework using seven species distribution models (SDMs), five climate scenarios and three emission and land‐use scenarios. We then compared results from SDMs using climate‐only variables, habitat‐only variables or both climate and habitat variables. In order to account for a species’ dispersal abilities, we used natal dispersal estimates and developed a probabilistic method that produced a dispersal scenario intermediate between the null and full dispersal scenarios generally considered in such studies. We then compared results from all scenarios in terms of future predicted range changes, range shifts, and variations in species richness. Modeling accuracy was better with climate‐only variables than with habitat‐only variables, and better with both climate and habitat variables. Habitat models predicted smaller range shifts and smaller variations in range size and species richness than climate models. Using both climate and habitat variables, it was predicted that the range of 71% of the species would decrease by 2050, with a 335 km median shift. Predicted variations in species richness showed large decreases in the southern regions of Europe, as well as increases, mainly in Scandinavia and northern Russia. The partial dispersal scenario was significantly different from the full dispersal scenario for 25% of the species, resulting in the local reduction of the future predicted species richness of up to 10%. We concluded that the breeding range of most European birds will decrease in spite of dispersal abilities close to a full dispersal hypothesis, and that given the contrasted predictions obtained when modeling climate change only and land‐use change only, both scenarios must be taken into consideration.  相似文献   

3.
Forecasting of species and ecosystem responses to novel conditions, including climate change, is one of the major challenges facing ecologists at the start of the 21st century. Climate change studies based on species distribution models (SDMs) have been criticized because they extend correlational relationships beyond the observed data. Here, we compared conventional climate‐based SDMs against ecohydrological SDMs that include information from process‐based simulations of water balance. We examined the current and future distribution of Artemisia tridentata (big sagebrush) representing sagebrush ecosystems, which are widespread in semiarid western North America. For each approach, we calculated ensemble models from nine SDM methods and tested accuracy of each SDM with a null distribution. Climatic conditions included current conditions for 1970–1999 and two IPCC projections B1 and A2 for 2070–2099. Ecohydrological conditions were assessed by simulating soil water balance with SOILWAT, a daily time‐step, multiple layer, mechanistic, soil water model. Under current conditions, both climatic and ecohydrological SDM approaches produced comparable sagebrush distributions. Overall, sagebrush distribution is forecasted to decrease, with larger decreases under the A2 than under the B1 scenario and strong decreases in the southern part of the range. Increases were forecasted in the northern parts and at higher elevations. Both SDM approaches produced accurate predictions. However, the ecohydrological SDM approach was slightly less accurate than climatic SDMs (?1% in AUC, ?4% in Kappa and TSS) and predicted a higher number of habitat patches than observed in the input data. Future predictions of ecohydrological SDMs included an increased number of habitat patches whereas climatic SDMs predicted a decrease. This difference is important for understanding landscape‐scale patterns of sagebrush ecosystems and management of sagebrush obligate species for future conditions. Several mechanisms can explain the diverging forecasts; however, we need better insights into the consequences of different datasets for SDMs and how these affect our understanding of future trajectories.  相似文献   

4.
Empirically derived species distributions models (SDMs) are increasingly relied upon to forecast species vulnerabilities to future climate change. However, many of the assumptions of SDMs may be violated when they are used to project species distributions across significant climate change events. In particular, SDM's in theory assume stable fundamental niches, but in practice, they assume stable realized niches. The assumption of a fixed realized niche relative to climate variables remains unlikely for various reasons, particularly if novel future climates open up currently unavailable portions of species’ fundamental niches. To demonstrate this effect, we compare the climate distributions for fossil‐pollen data from 21 to 15 ka bp (relying on paleoclimate simulations) when communities and climates with no modern analog were common across North America to observed modern pollen assemblages. We test how well SDMs are able to project 20th century pollen‐based taxon distributions with models calibrated using data from 21 to 15 ka. We find that taxa which were abundant in areas with no‐analog late glacial climates, such as Fraxinus, Ostrya/Carpinus and Ulmus, substantially shifted their realized niches from the late glacial period to present. SDMs for these taxa had low predictive accuracy when projected to modern climates despite demonstrating high predictive accuracy for late glacial pollen distributions. For other taxa, e.g. Quercus, Picea, Pinus strobus, had relatively stable realized niches and models for these taxa tended to have higher predictive accuracy when projected to present. Our findings reinforce the point that a realized niche at any one time often represents only a subset of the climate conditions in which a taxon can persist. Projections from SDMs into future climate conditions that are based solely on contemporary realized distributions are potentially misleading for assessing the vulnerability of species to future climate change.  相似文献   

5.
Species distribution models (SDMs) are an emerging tool in the study of fungi, and their use is expanding across species and research topics. To summarise progress to date and to highlight important considerations for future users, we review 283 studies that apply SDMs to fungi. We found that macrofungi, lichens, and pathogenic microfungi are most often studied. While many studies only aim to model species response to environmental covariates, the use of SDMs for explicitly predicting fungal occurrence in space and time is growing. Many studies collect fungal occurrence data, but the use of pre-collected records from reference collections and citizen science programs is increasing. Challenges of applying SDMs to fungi include detection and sampling biases, and uncertainties in identification and taxonomy. Further, finding environmental covariates at appropriate spatial and temporal scales is important, as fungi can respond to fine-scale environmental patterns. Fine-scale covariate data can be difficult to gather across space, but we show remote-sensing measurements are viable for fungi SDMs. For those fungi interacting with host species, host information is also important, and can be used as covariates in SDMs. We also highlight that competition among fungi, and dispersal, can affect observed distributions, with the latter particularly prominent for invasive fungi. We show how one can account for these processes in models, when suitable data are available. Finally, we note that environmental DNA records create new opportunities and challenges for future modelling efforts, and discuss the difficulties in predicting invasions and climate change impacts. The application of SDMs to fungi has already provided interesting lessons on how to adapt modelling tools for specific questions, and fungi will continue to be relevant test subjects for further technical development of SDMs.  相似文献   

6.
Species distribution models (SDMs) have rapidly evolved into one of the most widely used tools to answer a broad range of ecological questions, from the effects of climate change to challenges for species management. Current SDMs and their predictions under anthropogenic climate change are, however, often based on free‐air or synoptic temperature conditions with a coarse resolution, and thus fail to capture apparent temperature (cf. microclimate) experienced by living organisms within their habitats. Yet microclimate operates as soon as a habitat can be characterized by a vertical component (e.g. forests, mountains, or cities) or by horizontal variation in surface cover. The mismatch between how we usually express climate (cf. coarse‐grained free‐air conditions) and the apparent microclimatic conditions that living organisms experience has only recently been acknowledged in SDMs, yet several studies have already made considerable progress in tackling this problem from different angles. In this review, we summarize the currently available methods to obtain meaningful microclimatic data for use in distribution modelling. We discuss the issue of extent and resolution, and propose an integrated framework using a selection of appropriately‐placed sensors in combination with both the detailed measurements of the habitat 3D structure, for example derived from digital elevation models or airborne laser scanning, and the long‐term records of free‐air conditions from weather stations. As such, we can obtain microclimatic data with a relevant spatiotemporal resolution and extent to dynamically model current and future species distributions.  相似文献   

7.
Recent studies suggest that species distribution models (SDMs) based on fine‐scale climate data may provide markedly different estimates of climate‐change impacts than coarse‐scale models. However, these studies disagree in their conclusions of how scale influences projected species distributions. In rugged terrain, coarse‐scale climate grids may not capture topographically controlled climate variation at the scale that constitutes microhabitat or refugia for some species. Although finer scale data are therefore considered to better reflect climatic conditions experienced by species, there have been few formal analyses of how modeled distributions differ with scale. We modeled distributions for 52 plant species endemic to the California Floristic Province of different life forms and range sizes under recent and future climate across a 2000‐fold range of spatial scales (0.008–16 km2). We produced unique current and future climate datasets by separately downscaling 4 km climate models to three finer resolutions based on 800, 270, and 90 m digital elevation models and deriving bioclimatic predictors from them. As climate‐data resolution became coarser, SDMs predicted larger habitat area with diminishing spatial congruence between fine‐ and coarse‐scale predictions. These trends were most pronounced at the coarsest resolutions and depended on climate scenario and species' range size. On average, SDMs projected onto 4 km climate data predicted 42% more stable habitat (the amount of spatial overlap between predicted current and future climatically suitable habitat) compared with 800 m data. We found only modest agreement between areas predicted to be stable by 90 m models generalized to 4 km grids compared with areas classified as stable based on 4 km models, suggesting that some climate refugia captured at finer scales may be missed using coarser scale data. These differences in projected locations of habitat change may have more serious implications than net habitat area when predictive maps form the basis of conservation decision making.  相似文献   

8.
To study the potential effects of climate change on species, one of the most popular approaches are species distribution models (SDMs). However, they usually fail to consider important species‐specific biological traits, such as species’ physiological capacities or dispersal ability. Furthermore, there is consensus that climate change does not influence species distributions in isolation, but together with other anthropogenic impacts such as land‐use change, even though studies investigating the relative impacts of different threats on species and their geographic ranges are still rare. Here we propose a novel integrative approach which produces refined future range projections by combining SDMs based on distribution, climate, and physiological tolerance data with empirical data on dispersal ability as well as current and future land‐use. Range projections based on different combinations of these factors show strong variation in projected range size for our study species Emberiza hortulana. Using climate and physiological data alone, strong range gains are projected. However, when we account for land‐use change and dispersal ability, future range‐gain may even turn into a future range loss. Our study highlights the importance of accounting for biological traits and processes in species distribution models and of considering the additive effects of climate and land‐use change to achieve more reliable range projections. Furthermore, with our approach we present a new tool to assess species’ vulnerability to climate change which can be easily applied to multiple species.  相似文献   

9.
Aim To assess the effect of local adaptation and phenotypic plasticity on the potential distribution of species under future climate changes. Trees may be adapted to specific climatic conditions; however, species range predictions have classically been assessed by species distribution models (SDMs) that do not account for intra‐specific genetic variability and phenotypic plasticity, because SDMs rely on the assumption that species respond homogeneously to climate change across their range, i.e. a species is equally adapted throughout its range, and all species are equally plastic. These assumptions could cause SDMs to exaggerate or underestimate species at risk under future climate change. Location The Iberian Peninsula. Methods Species distributions are predicted by integrating experimental data and modelling techniques. We incorporate plasticity and local adaptation into a SDM by calibrating models of tree survivorship with adaptive traits in provenance trials. Phenotypic plasticity was incorporated by calibrating our model with a climatic index that provides a measure of the differences between sites and provenances. Results We present a new modelling approach that is easy to implement and makes use of existing tree provenance trials to predict species distribution models under global warming. Our results indicate that the incorporation of intra‐population genetic diversity and phenotypic plasticity in SDMs significantly altered their outcome. In comparing species range predictions, the decrease in area occupancy under global warming conditions is smaller when considering our survival–adaptation model than that predicted by a ‘classical SDM’ calibrated with presence–absence data. These differences in survivorship are due to both local adaptation and plasticity. Differences due to the use of experimental data in the model calibration are also expressed in our results: we incorporate a null model that uses survival data from all provenances together. This model always predicts less reduction in area occupancy for both species than the SDM calibrated with presence–absence. Main conclusions We reaffirm the importance of considering adaptive traits when predicting species distributions and avoiding the use of occurrence data as a predictive variable. In light of these recommendations, we advise that existing predictions of future species distributions and their component populations must be reconsidered.  相似文献   

10.
Species distribution models (SDMs) correlate species occurrences with environmental predictors, and can be used to forecast distributions under future climates. SDMs have been criticized for not explicitly including the physiological processes underlying the species response to the environment. Recently, new methods have been suggested to combine SDMs with physiological estimates of performance (physiology-SDMs). In this study, we compare SDM and physiology-SDM predictions for select marine species in the Mediterranean Sea, a region subjected to exceptionally rapid climate change. We focused on six species and created physiology-SDMs that incorporate physiological thermal performance curves from experimental data with species occurrence records. We then contrasted projections of SDMs and physiology-SDMs under future climate (year 2100) for the entire Mediterranean Sea, and particularly the ‘warm’ trailing edge in the Levant region. Across the Mediterranean, we found cross-validation model performance to be similar for regular SDMs and physiology-SDMs. However, we also show that for around half the species the physiology-SDMs substantially outperform regular SDM in the warm Levant. Moreover, for all species the uncertainty associated with the coefficients estimated from the physiology-SDMs were much lower than in the regular SDMs. Under future climate, we find that both SDMs and physiology-SDMs showed similar patterns, with species predicted to shift their distribution north-west in accordance with warming sea temperatures. However, for the physiology-SDMs predicted distributional changes are more moderate than those predicted by regular SDMs. We conclude, that while physiology-SDM predictions generally agree with the regular SDMs, incorporation of the physiological data led to less extreme range shift forecasts. The results suggest that climate-induced range shifts may be less drastic than previously predicted, and thus most species are unlikely to completely disappear with warming climate. Taken together, the findings emphasize that physiological experimental data can provide valuable supplemental information to predict range shifts of marine species.  相似文献   

11.
Statistical species distribution models (SDMs) are widely used to predict the potential changes in species distributions under climate change scenarios. We suggest that we need to revisit the conceptual framework and ecological assumptions on which the relationship between species distributions and environment is based. We present a simple conceptual framework to examine the selection of environmental predictors and data resolution scales. These vary widely in recent papers, with light inconsistently included in the models. Focusing on light as a necessary component of plant SDMs, we briefly review its dependence on aspect and slope and existing knowledge of its influence on plant distribution. Differences in light regimes between north‐ and south‐facing aspects in temperate latitudes can produce differences in temperature equivalent to moves 200 km polewards. Local topography may create refugia that are not recognized in many climate change SDMs using coarse‐scale data. We argue that current assumptions about the selection of predictors and data resolution need further testing. Application of these ideas can clarify many issues of scale, extent and choice of predictors, and potentially improve the use of SDMs for climate change modelling of biodiversity.  相似文献   

12.
Aim Species ranges have adapted during the Holocene to altering climate conditions, but it remains unclear if species will be able to keep pace with recent and future climate change. The goal of our study is to assess the influence of changing macroclimate, competition and habitat connectivity on the migration rates of 14 tree species. We also compare the projections of range shifts from species distribution models (SDMs) that incorporate realistic migration rates with classical models that assume no or unlimited migration. Location Europe. Methods We calibrated SDMs with species abundance data from 5768 forest plots from ICP Forest Level 1 in relation to climate, topography, soil and land‐use data to predict current and future tree distributions. To predict future species ranges from these models, we applied three migration scenarios: no migration, unlimited migration and realistic migration. The migration rates for the SDMs incorporating realistic migration were estimated according to macroclimate, inter‐specific competition and habitat connectivity from simulation experiments with a spatially explicit process model (TreeMig). From these relationships, we then developed a migration cost surface to constrain the predicted distributions of the SDMs. Results The distributions of early‐successional species during the 21st century predicted by SDMs that incorporate realistic migration matched quite well with the unlimited migration assumption (mean migration rate over Europe for A1fi/GRAS climate and land‐use change scenario 156.7 ± 79.1 m year?1 and for B1/SEDG 164.3 ± 84.2 m year?1). The predicted distributions of mid‐ to late‐successional species matched better with the no migration assumption (A1fi/GRAS, 15.2 ± 24.5 m year?1 and B1/SEDG, 16.0 ± 25.6 m year?1). Inter‐specific competition, which is higher under favourable growing conditions, reduced range shift velocity more than did adverse macroclimatic conditions (i.e. very cold or dry climate). Habitat fragmentation also led to considerable time lags in range shifts. Main conclusions Migration rates depend on species traits, competition, spatial habitat configuration and climatic conditions. As a result, re‐adjustments of species ranges to climate and land‐use change are complex and very individualistic, yet still quite predictable. Early‐successional species track climate change almost instantaneously while mid‐ to late‐ successional species were predicted to migrate very slowly.  相似文献   

13.
14.

Aim

Climate is considered a major driver of species distributions. Long‐term climatic means are commonly used as predictors in correlative species distribution models (SDMs). However, this coarse temporal resolution does not reflect local conditions that populations experience, such as short‐term weather extremes, which may have a strong impact on population dynamics and local distributions. We here compare the performance of climate‐ and weather‐based predictors in regional SDMs and their influence on future predictions, which are increasingly used in conservation planning.

Location

South‐western Germany.

Methods

We built different SDMs for 20 Orthoptera species based on three predictor sets at a regional scale for current and future climate scenarios. We calculated standard bioclimatic variables and yearly and seasonal sets of climate change indicating variables of weather extremes. As the impact of extreme events may be stronger for habitat specialists than for generalists, we distinguished species’ degrees of specialization. We computed linear mixed‐effects models to identify significant effects of algorithm, predictor set and specialization on model performance and calculated correlations and geographical niche overlap between spatial predictions.

Results

Current predictions were rather similar among all predictor sets, but highly variable for future climate scenarios. Bioclimatic and seasonal weather predictors performed slightly better than yearly weather predictors, though performance differences were minor. We found no evidence that specialists are more sensitive to weather extremes than generalists.

Main conclusions

For future projections of species distributions, SDM predictor selection should not solely be based on current performances and predictions. As long‐term climate and short‐term weather predictors represent different environmental drivers of a species’ distribution, we argue to interpret diverging future projections as complements. Even if similar current performances and predictions might imply their equivalency, favouring one predictor set neglects important aspects of future distributions and might mislead conservation decisions based on them.
  相似文献   

15.
Species distribution models (SDMs) are routinely applied to assess current as well as future species distributions, for example to assess impacts of future environmental change on biodiversity or to underpin conservation planning. It has been repeatedly emphasized that SDMs should be evaluated based not only on their goodness of fit to the data, but also on the realism of the modeled ecological responses. However, possibilities for the latter are hampered by limited knowledge on the true responses as well as a lack of quantitative evaluation methods. Here we compared modeled niche optima obtained from European-scale SDMs of 1476 terrestrial vascular plant species with empirical ecological indicator values indicating the preferences of plant species for key environmental conditions. For each plant species we first fitted an ensemble SDM including three modeling techniques (GLM, GAM and BRT) and extracted niche optima for climate, soil, land use and nitrogen deposition variables with a large explanatory power for the occurrence of that species. We then compared these SDM-derived niche optima with the ecological indicator values by means of bivariate correlation analysis. We found weak to moderate correlations in the expected direction between the SDM-derived niche optima and ecological indicator values. The strongest correlation occurred between the modeled optima for growing degree days and the ecological indicator values for temperature. Correlations were weaker for SDM-derived niche optima with a more distal relationship to ecological indicator values (notably precipitation and soil moisture). Further, correlations were consistently highest for BRT, followed by GLM and GAM. Our method gives insight into the ecological realism of modeled niche optima and projected core habitats and can be used to improve SDMs by making a more informed selection of environmental variables and modeling techniques.  相似文献   

16.
Species distribution models (SDMs) largely rely on free-air temperatures at coarse spatial resolutions to predict habitat suitability, potentially overlooking important microhabitat. Integrating microclimate data into SDMs may improve predictions of organismal responses to climate change and support targeting of conservation assets at biologically relevant scales, especially for small, dispersal-limited species vulnerable to climate-change-induced range loss. We integrated microclimate data that account for the buffering effects of forest vegetation into SDMs at a very high spatial resolution (3 m2) for three plethodontid salamander species in Great Smoky Mountains National Park (North Carolina and Tennessee). Microclimate SDMs were used to characterize potential changes to future plethodontid habitat, including habitat suitability and habitat spatial patterns. Additionally, we evaluated spatial discrepancies between predictions of habitat suitability developed with microclimate and coarse-resolution, free-air climate data. Microclimate SDMs indicated substantial losses to plethodontid ranges and highly suitable habitat by mid-century, but at much more conservative levels than coarse-resolution models. Coarse-resolution SDMs generally estimated higher mid-century losses to plethodontid habitat compared to microclimate models and consistently undervalued areas containing highly suitable microhabitat. Furthermore, microclimate SDMs revealed potential areas of future gain in highly suitable habitat within current species’ ranges, which may serve as climatic microrefugia. Taken together, this study highlights the need to develop microclimate SDMs that account for vegetation and its biophysical effects on near-surface temperatures. As microclimate datasets become increasingly available across the world, their integration into correlative and mechanistic SDMs will be imperative for accurately estimating organismal responses to climate change and helping environmental managers tasked with spatially prioritizing conservation assets.  相似文献   

17.
MJ Michel  JH Knouft 《PloS one》2012,7(9):e44932
When species distribution models (SDMs) are used to predict how a species will respond to environmental change, an important assumption is that the environmental niche of the species is conserved over evolutionary time-scales. Empirical studies conducted at ecological time-scales, however, demonstrate that the niche of some species can vary in response to environmental change. We use habitat and locality data of five species of stream fishes collected across seasons to examine the effects of niche variability on the accuracy of projections from Maxent, a popular SDM. We then compare these predictions to those from an alternate method of creating SDM projections in which a transformation of the environmental data to similar scales is applied. The niche of each species varied to some degree in response to seasonal variation in environmental variables, with most species shifting habitat use in response to changes in canopy cover or flow rate. SDMs constructed from the original environmental data accurately predicted the occurrences of one species across all seasons and a subset of seasons for two other species. A similar result was found for SDMs constructed from the transformed environmental data. However, the transformed SDMs produced better models in ten of the 14 total SDMs, as judged by ratios of mean probability values at known presences to mean probability values at all other locations. Niche variability should be an important consideration when using SDMs to predict future distributions of species because of its prevalence among natural populations. The framework we present here may potentially improve these predictions by accounting for such variability.  相似文献   

18.
Geospatial modeling is one of the most powerful tools available to conservation biologists for estimating current species ranges of Earth's biodiversity. Now, with the advantage of predictive climate models, these methods can be deployed for understanding future impacts on threatened biota. Here, we employ predictive modeling under a conservative estimate of future climate change to examine impacts on the future abundance and geographic distributions of Malagasy lemurs. Using distribution data from the primary literature, we employed ensemble species distribution models and geospatial analyses to predict future changes in species distributions. Current species distribution models (SDMs) were created within the BIOMOD2 framework that capitalizes on ten widely used modeling techniques. Future and current SDMs were then subtracted from each other, and areas of contraction, expansion, and stability were calculated. Model overprediction is a common issue associated Malagasy taxa. Accordingly, we introduce novel methods for incorporating biological data on dispersal potential to better inform the selection of pseudo‐absence points. This study predicts that 60% of the 57 species examined will experience a considerable range of reductions in the next seventy years entirely due to future climate change. Of these species, range sizes are predicted to decrease by an average of 59.6%. Nine lemur species (16%) are predicted to expand their ranges, and 13 species (22.8%) distribution sizes were predicted to be stable through time. Species ranges will experience severe shifts, typically contractions, and for the majority of lemur species, geographic distributions will be considerably altered. We identify three areas in dire need of protection, concluding that strategically managed forest corridors must be a key component of lemur and other biodiversity conservation strategies. This recommendation is all the more urgent given that the results presented here do not take into account patterns of ongoing habitat destruction relating to human activities.  相似文献   

19.
Predicting which species will occur together in the future, and where, remains one of the greatest challenges in ecology, and requires a sound understanding of how the abiotic and biotic environments interact with dispersal processes and history across scales. Biotic interactions and their dynamics influence species' relationships to climate, and this also has important implications for predicting future distributions of species. It is already well accepted that biotic interactions shape species' spatial distributions at local spatial extents, but the role of these interactions beyond local extents (e.g. 10 km2 to global extents) are usually dismissed as unimportant. In this review we consolidate evidence for how biotic interactions shape species distributions beyond local extents and review methods for integrating biotic interactions into species distribution modelling tools. Drawing upon evidence from contemporary and palaeoecological studies of individual species ranges, functional groups, and species richness patterns, we show that biotic interactions have clearly left their mark on species distributions and realised assemblages of species across all spatial extents. We demonstrate this with examples from within and across trophic groups. A range of species distribution modelling tools is available to quantify species environmental relationships and predict species occurrence, such as: (i) integrating pairwise dependencies, (ii) using integrative predictors, and (iii) hybridising species distribution models (SDMs) with dynamic models. These methods have typically only been applied to interacting pairs of species at a single time, require a priori ecological knowledge about which species interact, and due to data paucity must assume that biotic interactions are constant in space and time. To better inform the future development of these models across spatial scales, we call for accelerated collection of spatially and temporally explicit species data. Ideally, these data should be sampled to reflect variation in the underlying environment across large spatial extents, and at fine spatial resolution. Simplified ecosystems where there are relatively few interacting species and sometimes a wealth of existing ecosystem monitoring data (e.g. arctic, alpine or island habitats) offer settings where the development of modelling tools that account for biotic interactions may be less difficult than elsewhere.  相似文献   

20.
Weak climatic associations among British plant distributions   总被引:1,自引:0,他引:1  
Aim Species distribution models (SDMs) are used to infer niche responses and predict climate change‐induced range shifts. However, their power to distinguish real and chance associations between spatially autocorrelated distribution and environmental data at continental scales has been questioned. Here this is investigated at a regional (10 km) scale by modelling the distributions of 100 plant species native to the UK. Location UK. Methods SDMs fitted using real climate data were compared with those utilizing simulated climate gradients. The simulated gradients preserve the exact values and spatial structure of the real ones, but have no causal relationships with any species and so represent an appropriate null model. SDMs were fitted as generalized linear models (GLMs) or by the Random Forest machine‐learning algorithm and were either non‐spatial or included spatially explicit trend surfaces or autocovariates as predictors. Results Species distributions were significantly but erroneously related to the simulated gradients in 86% of cases (P < 0.05 in likelihood‐ratio tests of GLMs), with the highest error for strongly autocorrelated species and gradients and when species occupied 50% of sites. Even more false effects were found when curvilinear responses were modelled, and this was not adequately mitigated in the spatially explicit models. Non‐spatial SDMs based on simulated climate data suggested that 70–80% of the apparent explanatory power of the real data could be attributable to its spatial structure. Furthermore, the niche component of spatially explicit SDMs did not significantly contribute to model fit in most species. Main conclusions Spatial structure in the climate, rather than functional relationships with species distributions, may account for much of the apparent fit and predictive power of SDMs. Failure to account for this means that the evidence for climatic limitation of species distributions may have been overstated. As such, predicted regional‐ and national‐scale impacts of climate change based on the analysis of static distribution snapshots will require re‐evaluation.  相似文献   

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