There is an urgent need to develop e ective vulnerability assessments for evaluating the conservation status of species in a changing climate 1 . Several new assessment approaches have been proposed for evaluating the vulnerability of species to climate change 2-5 based on the expectation that established assessments such as the IUCN Red List 6 need revising or superseding in light of the threat that climate change brings. However, although previous studies have identified ecological and life history attributes that characterize declining species or those listed as threatened 7-9 , no study so far has undertaken a quantitative analysis of the attributes that cause species to be at high risk of extinction specifically due to climate change. We developed a simulation approach based on generic life history types to show here that extinction risk due to climate change can be predicted using a mixture of spatial and demographic variables that can be measured in the present day without the need for complex forecasting models. Most of the variables we found to be important for predicting extinction risk, including occupied area and population size, are already used in species conservation assessments, indicating that present systems may be better able to identify species vulnerable to climate change than previously thought. Therefore, although climate change brings many new conservation challenges, we find that it may not be fundamentally di erent from other threats in terms of assessing extinction risks.Attempts to quantify the threat that climate change poses to species' survival commonly infer extinction risk from changes in the area of climatically suitable habitat (the bioclimate envelope) 10,11 , but this approach ignores important aspects of species' biology such as population dynamics, vital rates and dispersal 12-16 , leading to high uncertainty 1,17 . To address this challenge, we coupled ecological niche models (ENMs) with demographic models [13][14][15][18][19][20] and expanded this approach by developing a generic life history (GLH) method. The coupled modelling approach estimates extinction risk as the probability of abundance falling to zero by the year 2100, rather than as the proportion of species committed to extinction due to contraction of bioclimate envelopes 10 (Methods).By matching ENMs for 36 amphibian and reptile species endemic to the US with corresponding GLH models (Supplementary Table 1), we estimate mean extinction risk by 2100 to be 28 ± 7% under a high CO 2 concentration Reference climate scenario 21 and 23 ± 7% under a Policy climate scenario that assumes substantive intervention 22 (Methods). In contrast, extinction risk is estimated by the same models to be <1% without climate change, showing that the methods are not biased towards predicting high risks. The contrast between predicted extinction risk with and without climate change suggests that climate change will cause a pronounced increase in extinction risk for these taxonomic groups over the coming century. Contrary to other stud...
We link spatially explicit climate change predictions to a dynamic metapopulation model. Predictions of species' responses to climate change, incorporating metapopulation dynamics and elements of dispersal, allow us to explore the range margin dynamics for two lagomorphs of conservation concern. Although the lagomorphs have very different distribution patterns, shifts at the edge of the range were more pronounced than shifts in the overall metapopulation. For Romerolagus diazi (volcano rabbit), the lower elevation range limit shifted upslope by approximately 700 m. This reduced the area occupied by the metapopulation, as the mountain peak currently lacks suitable vegetation. For Lepus timidus (European mountain hare), we modelled the British metapopulation. Increasing the dispersive estimate caused the metapopulation to shift faster on the northern range margin (leading edge). By contrast, it caused the metapopulation to respond to climate change slower, rather than faster, on the southern range margin (trailing edge). The differential responses of the leading and trailing range margins and the relative sensitivity of range limits to climate change compared with that of the metapopulation centroid have important implications for where conservation monitoring should be targeted. Our study demonstrates the importance and possibility of moving from simple bioclimatic envelope models to second-generation models that incorporate both dynamic climate change and metapopulation dynamics.
Models that couple habitat suitability with demographic processes offer a potentially improved approach for estimating spatial distributional shifts and extinction risk under climate change. Applying such an approach to five species of Australian plants with contrasting demographic traits, we show that: (i) predicted climate‐driven changes in range area are sensitive to the underlying habitat model, regardless of whether demographic traits and their interaction with habitat patch configuration are modeled explicitly; and (ii) caution should be exercised when using predicted changes in total habitat suitability or geographic extent to infer extinction risk, because the relationship between these metrics is often weak. Measures of extinction risk, which quantify threats to population persistence, are particularly sensitive to life‐history traits, such as recruitment response to fire, which explained approximately 60% of the deviance in expected minimum abundance. Dispersal dynamics and habitat patch structure have the strongest influence on the amount of movement of the trailing and leading edge of the range margin, explaining roughly 40% of modeled structural deviance. These results underscore the need to consider direct measures of extinction risk (population declines and other measures of stochastic viability), as well as measures of change in habitat area, when assessing climate change impacts on biodiversity. Furthermore, direct estimation of extinction risk incorporates important demographic and ecosystem processes, which potentially influence species’ vulnerability to extinction due to climate change.
It has been difficult to access projections of global-scale climate change with high temporal resolution spaning the late Pleistocene and Holocene. This has limited our ability to discern how climate fluctuations have affected species' range dynamics and extinction processes, turn-over in ecological communities and changes in genetic diversity. PaleoView is a new freeware tool, which provides a comprehensive but easy-to-use way to generate and view paleoclimate data at temporal and spatial resolutions suitable for detecting biotic responses to major climate shifts since the last glacial maximum. Regional to global scale simulations of temperature, precipitation, humidity and mean sea level pressure can be generated from PaleoView as gridded or time series data at time intervals as short as a decade for any period during the last 21 000 yr. They can be viewed using a built-in geographical user interface or saved as data files. Modelled climate reconstructions are based on daily simulation output from the Community Climate System Model ver. 3 (CCSM3). This global coupled atmosphere-ocean-sea ice-land general circulation model accurately reproduces major climatic features associated with the most recent deglaciation event, and predicts present-day patterns of climate conditions with verified hindcast skill. By providing a portal for readily accessing climate reconstructions at high temporal resolutions, PaleoView can help to better establish the consequences of past climate fluctuations on macro-ecological patterns of biological and genetic diversity.
Aim Understanding the relative importance of climatic and non‐climatic distribution drivers for co‐occurring, functionally similar species is required to assess potential consequences of climate change. This understanding is, however, lacking for most ecosystems. We address this knowledge gap and forecast changes in distribution for habitat‐forming seaweeds in one of the world's most species‐rich temperate reef ecosystems. Location The Great Southern Reef. The full extent of Australia's temperate coastline. Methods We assessed relationships between climatic and non‐climatic environmental data known to influence seaweed, and the presence of 15 habitat‐forming seaweeds. Distributional data (herbarium records) were analysed with MAXENT and generalized linear and additive models, to construct species distribution models at 0.2° spatial resolution, and project possible distribution shifts under the RCP 6.0 (medium) and 2.6 (conservative) emissions scenarios of ocean warming for 2100. Results Summer temperatures, and to a lesser extent winter temperatures, were the strongest distribution predictors for temperate habitat‐forming seaweeds in Australia. Projections for 2100 predicted major poleward shifts for 13 of the 15 species, on average losing 78% (range: 36%–100%) of their current distributions under RCP 6.0 and 62% (range: 27%–100%) under RCP 2.6. The giant kelp (Macrocystis pyrifera) and three prominent fucoids (Durvillaea potatorum, Xiphophora chondrophylla and Phyllospora comosa) were predicted to become extinct from Australia under RCP 6.0. Many species currently distributed up the west and east coasts, including the dominant kelp Ecklonia radiata (71% and 49% estimated loss for RPC 6.0 and 2.6, respectively), were predicted to become restricted to the south coast. Main conclusions In close accordance with emerging observations in Australia and globally, our study predicted major range contractions of temperate seaweeds in coming decades. These changes will likely have significant impacts on marine biodiversity and ecosystem functioning because large seaweeds are foundation species for 100s of habitat‐associated plants and animals, many of which are socio‐economically important and endemic to southern Australia.
Global warming and ocean acidification are forecast to exert significant impacts on marine ecosystems worldwide. However, most of these projections are based on ecological proxies or experiments on single species or simplified food webs. How energy fluxes are likely to change in marine food webs in response to future climates remains unclear, hampering forecasts of ecosystem functioning. Using a sophisticated mesocosm experiment, we model energy flows through a species-rich multilevel food web, with live habitats, natural abiotic variability, and the potential for intra- and intergenerational adaptation. We show experimentally that the combined stress of acidification and warming reduced energy flows from the first trophic level (primary producers and detritus) to the second (herbivores), and from the second to the third trophic level (carnivores). Warming in isolation also reduced the energy flow from herbivores to carnivores, the efficiency of energy transfer from primary producers and detritus to herbivores and detritivores, and the living biomass of detritivores, herbivores, and carnivores. Whilst warming and acidification jointly boosted primary producer biomass through an expansion of cyanobacteria, this biomass was converted to detritus rather than to biomass at higher trophic levels—i.e., production was constrained to the base of the food web. In contrast, ocean acidification affected the food web positively by enhancing trophic flow from detritus and primary producers to herbivores, and by increasing the biomass of carnivores. Our results show how future climate change can potentially weaken marine food webs through reduced energy flow to higher trophic levels and a shift towards a more detritus-based system, leading to food web simplification and altered producer–consumer dynamics, both of which have important implications for the structuring of benthic communities.
Ecological niche models (ENMs) are the primary tool used to describe and forecast the potential influence of climate change on biodiversity. However, ENMs do not directly account for important biological and landscape processes likely to affect range dynamics at a variety of spatial scales. Recent advances to link ENMs with population models have focused on the fundamental step of integrating dispersal and metapopulation dynamics into forecasts of species geographic ranges. Here we use a combination of novel analyses and a synthesis of findings from published plant and animal case studies to highlight three seldom recognised, yet important, advantages of linking ENMs with demographic modelling approaches: 1) they provide direct measures of extinction risk in addition to measures of vulnerability based on change in the potential range area or total habitat suitability. 2) They capture life‐history traits that permit population density to vary in different ways in response to key spatial drivers, conditioned by the processes of global change. 3) They can be used to explore and rank the cost effectiveness of regional conservation alternatives and demographically oriented management interventions. Given these advantages, we argue that coupled methods should be used preferentially where data permits and when conservation management decisions require intervention, prioritization, or direct estimates of extinction risk.
The Iberian lynx (Lynxpardinus) has suffered severe population declines in the twentieth century and is now on the brink of extinction 1 . Climate change could further threaten the survival of the species 2 , but its forecast effects are being neglected in recovery plans 3,4 . Quantitative estimates of extinction risk under climate change have so far mostly relied on inferences from correlative projections of species' habitat shifts 5 . Here we use ecological niche models coupled to metapopulation simulations with source-sink dynamics 6,7 to directly investigate the combined effects of climate change, prey availability and management intervention on the persistence of the Iberian lynx. Our approach is unique in that it explicitly models dynamic bi-trophic species interactions in a climate change setting. We show that anticipated climate change will rapidly and severely decrease lynx abundance and probably lead to its extinction in the wild within 50 years, even with strong global efforts to mitigate greenhouse gas emissions. In stark contrast, we also show that a carefully planned reintroduction programme, accounting for the effects of climate change, prey abundance and habitat connectivity, could avert extinction of the lynx this century. Our results demonstrate, for the first time, why considering prey availability, climate change and their interaction in models is important when designing policies to prevent future biodiversity loss.The 9 Rui Nabeiro Biodiversity Chair, CIBIO, University of Évora, Évora, 7000, Portugal, 10 Center for Macroecology, Evolution and Climate, University of Copenhagen, 2100 Copenhagen, Denmark. *e-mail: maraujo@mncn.csic.es towards increasing the carrying capacity of reintroduction sites through habitat restoration, relocating rabbits and limiting direct anthropogenic-related fatalities 4,13 .Although a well-financed effort to avert the extinction of this charismatic species is underway (> e94 million funding since 1994) 4 , non-accounted threats, such asclimatechangeanditsinfluenceonpreyabundance,arenotbeing considered in recovery plans.Here we provide the most comprehensive analysis of the likely effects of climate change yet for a threatened vertebrate. So far, models used to investigate how climate change will
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