International policy is placing increasing emphasis on adaptation to climate change, including the allocation of new funds to assist adaptation efforts. Climate change adaptation funding may be most effective where it meets integrated goals, but global geographic priorities based on multiple development and ecological criteria are not well characterized. Here we show that human and natural adaptation needs related to maintaining agricultural productivity and ecosystem integrity intersect in ten major areas globally, providing a coherent set of international priorities for adaptation funding. An additional seven regional areas are identified as worthy of additional study. The priority areas are locations where changes in crop suitability affecting impoverished farmers intersect with changes in ranges of restricted-range species. Agreement among multiple climate models and emissions scenarios suggests that these priorities are robust. Adaptation funding directed to these areas could simultaneously address multiple international policy goals, including poverty reduction, protecting agricultural production and safeguarding ecosystem services.
Citation: Hannah L, Ikegami M, Hole DG, Seo C, Butchart SHM, et al. (2013) Global Climate Change Adaptation Priorities for Biodiversity and Food Security. PLoS ONE 8(8): e72590. doi:10.1371/journal.pone.0072590
Editor: Alex J Cannon, Pacific Climate Impacts Consortium, Canada
Received: November 13, 2012; Accepted: July 14, 2013; Published: August 21, 2013
Copyright: © 2013 Hannah et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The authors have no support or funding to report.
Competing interests: The authors have declared that no competing interests exist.
The need for adaptation to climate change is an emerging focus of international policy . The impacts of climate change are already being felt from the tropics (e.g., small island states, coral reefs) to the arctic (e.g., first nations communities) . New international funding is being mobilized to meet these new challenges, but the committed funds are still likely an order of magnitude less than the medium-term needs . As a result, recently committed funding needs to be prioritized to areas with exceptional need and/or the potential for impact in multiple sectors simultaneously .
Ecosystem-based Adaptation is the use of ecosystem services to help people adapt to climate change. Intact ecosystems provide clean water, shoreline protection, and other services in the face of climate change, providing adaptation options that are often cheaper and more enduring than technical or engineering solutions . Maintaining intact ecosystems benefits both human adaptation to climate change and biodiversity. Understanding linkages between sectors is an important first step toward realizing these benefits.
Priorities linking ecosystems and food production are particularly important because human and natural responses to climate change are interwoven [6–8]. Impoverished farmers are likely to use diverse livelihood strategies that include diverse natural ecosystems and agro-ecosystems , and that benefit from a range of ecosystem services [10,11]. Individual species’ range shifts can break up plant and animal communities, altering ecosystem services critical to agriculture, such as watershed protection . Decline in agricultural productivity due to climate change can lead to crop expansion into nearby natural habitats as farmers attempt to compensate for lost yield by increasing area under production. This may result in biodiversity loss, as well as undermining the very ecosystem services that support agriculture . Understanding of these inter-dependencies under climate change is emerging [14–16]. Subsistence farmers most sensitive to climate change are in the tropics [16,17], as are the species most sensitive to climate change [14,18,19]. Critical areas in which the axes of agricultural and ecosystem responses to climate change intersect are beginning to be documented for individual regions [10,20].
Adaptation action in these areas could simultaneously enhance food security and maintain ecosystem function. This has policy relevance on multiple levels, as food security and ecosystem integrity are two of the three major benchmarks for climate change response established in the United Nations Framework Convention on Climate Change (UNFCCC), and make substantial contribution towards sustainable development, thus helping meet all three UNFCCC criteria . However, studies examining the interlinkage of agriculture and ecosystem change on a global scale are lacking.
Here we model changes in food production and biodiversity to find areas in which adaptation needs are high in both sectors. Our models focus on 1) rainfed agriculture which supports many of the world’s poorest farmers  and 2) restricted-range bird species (i.e., historical range <50,000 km2) which are indicative of highly complex and biodiverse ecosystems [23,24]. We find multiple areas in which declining crop productivity and shifts in restricted-range species coexist, indicating possible synergies between ecosystem health and human well-being. We suggest that these areas are a valuable initial set of priorities for research and action in climate change adaptation.
Materials and Methods
We assessed declines in agricultural suitability and in the distribution of restricted-range bird species resulting from climate change for 15 major rainfed staple crops and 1,263 restricted-range bird species, using five general circulation models (GCM). We modeled change in climate suitability for the rainfed subsistence crops that are of greatest importance for poor farmers in each region. Data on crop climatic tolerances were extracted from the EcoCrop Dataset . Species distribution models (SDM) were used to simulate range changes in response to climate change for 1,263 restricted-range bird species using a global database of occurrence records . Restricted-range bird species were chosen as modeling subjects as they represent unique elements in regional ecosystems, have small range sizes that make them vulnerable to climate change  and are used to define areas of high ecological priority such as endemic bird areas and global biodiversity hotspots [23,25]. Ecosystem and agricultural adaptation priorities were defined as regions in the upper quartile (>25%) in terms of species losing range or crops losing suitability under climate change. We then aggregated results to identify areas where these crop and ecosystem adaptation priorities are in close proximity. We indicated level of agreement between GCMs using an ensemble histogram approach in which level of agreement is indicated by mapped color intensity. Agricultural priorities, ecosystem priorities and cells with combined priority are mapped with GCM agreement indicated by five color increments corresponding to level of agreement among the five GCMs used.
Species distribution modeling approach
Species distribution models (SDMs) simulate distributions of species based on the association of their current range with climatic variables, and may be used to simulate future ranges under climate change. Because many SDM methods are available, we tested the effect of a range of SDMs on our results. We implemented seven SDMs that have previously been shown to be effective in modeling the distributions of a range of taxa : Maxent ; classification tree analysis (CTA); generalized additive models (GAM) ; generalized boosted regression models (GBR) ; generalized linear models (GLM) ; multivariate additive regression splines (MARS) , and random forests (RF) . All SDMs except Maxent were developed within the R module BIOMOD . Absence data for CTA, GAM, GBR, GLM, MARS, and RF were generated from individual species’ range maps, taking random points within a 500km buffer of known occurrences. The occurrence data were divided, 70% for model construction and 30% for model evaluation. To produce binary maps from SDM output, we used maximized training sensitivity plus specificity values for Maxent while the area under the curve (AUC) of the receiver operating characteristic (ROC) plot was used to determine optimal thresholds for the other SDMs.
We chose six variables as climatic inputs for the SDMs, including maximum and minimum temperature, precipitation seasonality, precipitation of the warmest quarter, growing degree days above 5°C (GDD), and an aridity index. Precipitation seasonality measures the variability of precipitation throughout the year, helping distinguish between tropical, Mediterranean and temperate climates. The aridity index incorporates the effects of both precipitation and temperature on moisture availability. These climatic variables may be directly relevant to the bird species being modeled (e.g., minimum temperature), the habitats on which these birds depend (e.g., GDD), or both.
We evaluated model performance by comparing SDM output with the range map of each species using specificity, sensitivity, Kappa , True Skill Statistic (TSS) , and Matthews’ correlation coefficient (MCC) . Maxent models showed the best performance in all criteria except sensitivity. We constructed final global priorities using each individual SDM and found that regions identified were identical across all seven SDM variants, although the specific species range simulations varied. The results reported here are from the Maxent SDM.
Restricted-range species distribution data
We used comprehensive unique georeferenced point localities from BirdLife International’s World Bird Database for restricted-range terrestrial bird species  as input for all SDMs. For quality control we omitted occurrence points that fell outside each species’ known extent of occurrence (EOO) , buffered by 20 km. EOO was determined by expert opinion informed by the point data augmented by information in the published literature (field guides, family monographs, national distribution atlases, specific inventories and surveys), observer records (e.g. from www.worldbirds.org), and data from the Global Biodiversity Information Facility (www.gbif.org). The points are of variable precision depending on date of acquisition, but typically accurate to within 1-2 km. Species with <13 point localities were excluded from the analysis because SDM reliability declines at low numbers of occurrence points. The resulting final data set included 1,263 species that were modeled for this analysis.
Agricultural suitability modeling approach
Global suitability for the 15 agricultural crops (Table 1) was modeled using crop environmental requirements defined by FAO’s EcoCrop database . EcoCrop defines optimal growing conditions for a crop relative to multiple climatic parameters. We considered a region suitable for a crop where conditions were at least 50% of optimal, based on a linear interpolation between the conditions for optimal growth and the absolute limit to growth for that crop as defined in EcoCrop (see Table S1). We used the Spatial Production Allocation Model, which delineates crops currently grown in individual regions, to select crops for modeling . Only crops currently grown in a region were modeled, since the need for adaptation is best measured as decline in crops actually produced. This approach builds on global modeling of agricultural suitability using EcoCrop in Lane and Jarvis (2007) .
|common name||Scientific name|
|Barley||Hordeum vulgare L.|
|Common bean||Phaseolus vulgaris L.|
|Sugar cane||Saccharum spp.2|
|Cassava||Manihot esculenta Crantz.|
|Maize||Zea mays L3|
|Millet||Panicum miliaceum L.|
|Ground nut||Arachis spp.4|
|Potato||Solanum tuberosum L.|
|Rice||Oryza sativa L.5|
|Sorghum||Sorghum bicolor (L.)|
|Soybean||Glycine max (L.) Merrill|
|Sugar beet||Beta vulgaris L|
|Sweet potato||Ipomoea batatas (L.) Lam.|
The environmental requirements for individual crops are defined in EcoCrop by optimal ranges of maximum and minimum temperature, precipitation, and length of growing season (Table S1). We used the full range of environmental requirements spanning all varieties of each staple crop. We included a proxy for CO2 fertilization by adjusting water use efficiency through a linear interpolation of experiment-derived efficiency gains for both C3 and C4 crops . Crop production was considered ‘lost’ when a crop’s suitability declined >50% within a grid cell. We evaluated crop suitability loss in a global grid, and determined the ratio of crops losing suitability to the number of crops currently grown for each grid cell.
Projections of future climate were obtained from transient simulations of five GCMs: MIROC3.2 (medium resolution), CSIRO Mk3.5, BCM2.0, CCSM3.0, INMCM3.0 selected to represent a range of global mean temperature change projections and regional precipitation change patterns. All models were implemented under two emissions scenarios (A2 and B1)  and two future time periods (20 year averages centered on 2050 and 2090). For each GCM and emissions scenario, temperature and precipitation anomalies between present and future time periods were interpolated to 2.5 arc-minute horizontal resolution and added to historical values from the WorldClim 1950-2000 database to produce simulated future climates . Regional and global priority areas remained the same in the 2050 and 2090 scenarios, and global priorities remained the same across A2 and B1 scenarios, so only 2090 A2 results are reported here.
Identifying adaptation priority regions
Based on current climate and modeled future climate scenarios, we calculated the number of bird species that lose climatic suitability in each 2.5 arc-minute grid cell for each future time step. The upper quartile (top 25%) of cells in terms of total species losing range were categorized as ecosystem adaptation priority areas. Similarly, agricultural adaptation priority areas were defined based on the upper quartile of cells in number of crops lost. To identify combined adaptation priority areas, we overlaid a one-degree grid on the 2.5 arc-minute agricultural and ecosystem adaptation priority cells. The resulting one-degree cells that contained both agricultural and ecosystem adaptation priority areas were used to identify global and regional adaptation priority areas.
Global adaptation priorities were defined by high GCM agreement (4-5 GCMs) on co-occurrence of ecosystem and agricultural adaptation priority in individual one-degree cells, together with adjacent areas of agricultural or species priority. These global priority areas have large crop and species change in close proximity and are therefore good candidates for multi-purpose adaptation funding. Regional priorities are areas with lower GCM agreement (1-3 GCMs) on combined crop and species priorities along with adjacent areas of agricultural and species priority. These regional priorities may be important locally or warrant additional research to more firmly establish coincidence of agricultural and ecosystem change. Where two global priorities or a global priority and regional priority co-occurred within a national boundary or ecoregion, they were combined (e.g., Atlantic Coast of Brazil).
Ten global priority areas for adaptation funding can be identified based on intersection of changes in agricultural suitability and climatic suitability for restricted-range species (Figure 1). The ten areas comprise 9.3% of the world’s habitable lands and 10.6% of remaining natural habitats; 7-9% of the world’s poor inhabit these areas and all of the areas intersect global biodiversity hotspots (Table 2). The agricultural and ecological changes that define these areas include declines in rainfed agricultural suitability encompassing 8.9% of the world’s arable land and 12.8% of currently cultivated land in the tropics and 69% of all modeled restricted-range bird species. Investment in these areas of intersecting suitability decline can help address the intertwined adaptation needs of agriculture and biodiversity.
Global priorities (solid outlines) are areas of overlapping or contiguous agricultural and ecosystem change that appear by mid-century (2050). Regional priorities (broken circles) are areas of agricultural and ecological change that are less extensive and appear only later in the century (2090 scenarios). These global and regional priorities illustrated here are superimposed on a base map of 2090 A2 changes in both crops and restricted-range birds. Areas in which overall decreases are anticipated in crop suitability are shown in green, with increasing color intensity indicating multiple GCM agreement. Areas of declining climatic suitability for restricted-range birds are shown in blue, with increasing color intensity indicating multiple GCM agreement. Overlap of declining crop suitability and declining restricted-range bird climatic suitability is shown in shades of yellow (lowest GCM agreement) to red (highest GCM agreement).
|Global Adaptation Priorities||crop loss(max %) *||bird suitability loss (%)**||area (km2)||population(1000)||poverty index (average)||globalhunger index||Nations||# of global 200 ecoregions||global biodiversity hotspots|
|1||Central America||100.0||55.6||656,678||43,637||13.3||9.9||Mexico; Guatemala;Honduras; Nicaragua||3||Mesoamerica;Madrean pine-oak woodlands|
|2||Caribbean||100.0||54.0||96,575||22,603||28.0||18.6||Jamaica; Haiti;Dominica, Puerto Rico||2||Caribbean Islands;|
|3||Andes||100.0||44.9||2,931,172||93,053||12.0||7.4||Venezuela; Colombia/Ecuador; Peru; Bolivia; Argentina||17||Tumbes-Chocó-MagdalenaTropical Andes|
|4||Guiana Highlands||43.6||62.8||302,352||282||12.0||6.1||Venezuela||3||Tropical Andes|
|5||Atlantic Coast of Brazil||100.0||40.5||1,507,802||107,364||6.0||0.0||Brazil||3||Atlantic Forest|
|6||Albertine Rift||41.8||64.7||459,924||34,641||41.8||26.0||Zaire; Burundi; Tanzania; Uganda||6||Eastern Afromontane|
|7||Madagascar||93.4||78.0||587,041||16,194||35.0||27.5||Madagascar||4||Madagascar and the Indian Ocean Islands|
|8||Western Ghats||85.3||50.7||328,376||107,074||22.0||13.2||India||1||Western Ghats Sri Lanka|
|r1||Northwest Mexico||80.0||66.7||149,589||2,234||4.0||<5||Mexico||3||Mesoamerica;Madrean pine-oak woodlands|
|r2||West Africa||15.4||77.8||337,507||18,655||14.0||14.0||Ivory Coast||1||Guinean Forests of West Africa|
|r3||Cross river||22.5||64.3||129,285||6,745||15.5||17.7||Cameroon; Nigeria||3||Guinean Forests of West Africa|
|r5||Eastern Himalaya||68.7||60.0||582,384||68,840||21.7||22.4||India; Myanmar; Bhutan (Bangladesh)||6||Himalaya|
|r7||New Guinea||74.9||62.2||786,000||6,721||16.0||13.2||Papua New Guinea, Indonesia||6||Himalaya; Indo-Burma|
|* Maximum % crop loss denotes the highest crop loss in any cell in the region. ** Cumulative % restricted-range bird loss of climatic suitability is the sum of total suitable area across all species in 2090 as a percentage of the sum of total suitable area across all species in 2000.|
An additional seven regional priority areas harbor both agricultural and natural change that is less certain (i.e. less GCM agreement) than in the ten global priorities and therefore represent research priorities for more detailed regional analysis. These areas are Northwest Mexico, West Africa, the Cross River region, the Western Himalayas, the Eastern Himalayas, Sulawesi, and New Guinea. Most of these areas experience upper quartile crop loss or habitat suitability loss under most GCM scenarios, but with little inter-GCM agreement on areas of overlap.
The analyses used to derive these priorities are robust to alternative analytical methods, climate scenarios and climate models. The ensemble histogram approach used here (see Figures S1-S6)  presents the degree of agreement across multiple GCMs. The orange-red color ramp in Figure 1 indicates areas in which combined crop and ecosystem adaptation priorities are found in all five GCM results (red) through decreasing GCM agreement to combined crop and ecosystem priority found in only one GCM result (yellow). GCM agreement on non-overlapping agricultural and ecosystem adaptation priorities are shown in color ramps of green (crop loss) and blue (species range loss). This histogram approach highlights priorities that emerge repeatedly across multiple climate models, and are thus more robust to GCM uncertainty . This ensemble histogram , in which GCM agreement is explicitly represented, contrasts with the ensemble mean approach in which the average of GCM results is taken. The ensemble histogram maintains relationships between climatic variables within individual GCMs, allowing representation of variable interactions that might be lost in an ensemble mean, for instance between temperature and precipitation in determining soil moisture. We have tested the ensemble histogram against ensemble mean approaches (Figures S4 and S5), and found that ensemble mean priorities are a subset of those determined using ensemble histograms. The priorities in Central and South America are robust across both methods, while the ensemble mean shows few priorities in Africa or Asia at the thresholds used here.
Uncertainty associated with species and agricultural modeling is more difficult to constrain. In the tropics, species ranges may not sample all climatic conditions that are physiologically tolerable, resulting in over-estimation of range loss. Adaptation priorities for non-avian restricted-range species may not match those for birds, due to different taxonomic climatic tolerances. SDM are fitted to empirical data using current climatic conditions and may not simulate future range changes well when future climatic conditions are outside the range of current climate. Adaptation in agriculture may moderate crop losses, resulting in over-estimation of crop impacts. For instance, consumption may switch to crops which may be grown in a region but are not culturally favored, once suitability for preferred crops declines. For these reasons, regional analyses incorporating social factors, taxa other than birds, and analyses of adaptation capacity are essential complements to this global analysis.
The priorities identified here reinforce and expand on the findings of other research into agricultural and biodiversity responses to climate change. Areas of agricultural vulnerability identified in this study overlap with those defined in other global assessments of agricultural impacts of climate change [44–46]. For instance, the Indian sub-continent emerges as an area of agricultural decline in both our results and in those of other studies [22,46]. Ecologically vulnerable areas identified in our restricted-range bird modeling are broadly consistent with impacts projected in several recent studies [47–49].
Possible adaptation responses in these priority areas might include actions that integrate adaptation for agriculture and ecosystems. For instance, agroforestry can help reduce soil temperatures and maintain soil moisture as air temperatures increase, and, with the appropriate choice of tree species, can help provide habitat for restricted-range birds and other wildlife. Protecting upland forests that provide fog interception or provide watershed protection for dams may be critical for agriculture in areas of declining precipitation, at the same time providing habitats that will permit range migrations in forest birds responding to climate change. Many of these solutions require planning on scales broader than individual farms or protected areas, which is why we have aggregated our results at spatial scales roughly coincident with scales of ecosystem and regional planning (one degree).
It is likely that finer-grained analyses will confirm some or all of the regional priority areas identified (dashed outlines, Figure 1) as regions of considerable change in both agriculture and ecosystems. For instance, in this study, the island of New Guinea (Indonesian Papua and Papua New Guinea) showed high change in restricted-range birds but little agricultural change. However, this region has very limited agricultural data because the subsistence crops prevalent there are poorly captured in global agricultural records. It is likely that improved agricultural data would reveal high adaptation needs in agriculture in this area, making it a joint priority for both human and natural adaptation.
The global adaptation priorities defined here have important policy relevance. First, they highlight areas in which it is most critical to address cross-sector inter-dependencies to achieve lasting adaptation results. Second, they illustrate a broader set of solutions to planning problems that must balance short-term human adaptation needs with long-term ecological sustainability. Finally, they help guide investment toward regions that may serve as tests for planning and adaptation solutions that can evolve to help other regions simultaneously meet multiple objectives of international agreements.
The UNFCCC holds as its goal the prevention of dangerous anthropogenic interference in the climate system, “within a time-frame sufficient to allow ecosystems to adapt naturally to climate change, to ensure that food production is not threatened and to enable economic development to proceed in a sustainable manner” [21,50]. Our results show that food production and ecosystem integrity are jointly vulnerable in ten world regions. Because global political progress on climate change mitigation is evolving slowly at present , it is probable that adaptation actions in these regions will be the only means of averting the kind of damage to human and natural systems that the world has committed to avoid in the climate convention.
Adaptation investments in these regions will, at the same time, realize progress towards achieving Millennium Development Goals and the goals of the Convention on Biological Diversity. The global and regional adaptation priority regions combined hold over 10% of the world population living in poverty, typically at less than half of the global average Human Development Index (Table 2). Targeting these areas can help meet the need for global adaptation funding priorities, as well as address poverty alleviation. The biodiversity in these areas is of global importance, as all are recognized in one or more global conservation priority ranking systems (e.g., hotspots, Global 200 ecoregions – see Table 2). Investment in these areas can help pioneer demonstrations that human development and ecological sustainability are intertwined - even more intimately than at present - as climate changes.
Designing adaptation investment strategies to meet these cross-sectoral goals requires decisions at multiple scales. This analysis provides a first set of global investment priorities. At the local scale, investments that capitalize on these opportunities may come through land sharing, in which case single investments can address both priorities, or through land sparing, in which case separate investments (each with strong links to the other sector) will be required. Both approaches can be effective , so wise investment requires sufficient understanding of local social and biological circumstances to know which will be most effective.
Adaptation practice is currently being pioneered in first-generation projects around the world. These efforts are addressing the adaptation needs of communities and ecosystems, increasingly recognizing deep interdependencies between the two. Meeting short-term development needs while establishing long-term sustainability of ecosystem services is a fundamental challenge. Among the best places to build experience in melding human and ecosystem responses will be regions experiencing substantial change in both. Innovative solutions and lessons from these areas can inform second-generation adaptation responses worldwide. Investment in the priority regions identified here is therefore a first step in developing a lasting, multi-sector approach to adaptation.
Species and parameters used for EcoCrop modeling. Some crop species contained different species and varieties, so the model adapted the widest range of environmental requirement among species/varieties. The list of species used in the model appears below the table. Minimum and maximum temperature/precipitation requirements represent the environmental range where crop growth is possible and optimal minimum and maximum temperature/precipitation requirements are the environmental range of optimal growth.
Performance of each SDM tested by overall accuracy, Kappa, TSS, MCC, specificity and sensitivity. Maxent scored highest performance except sensitivity that RF scored the highest performance.
Global map of crop suitability and suitability for range restricted birds change in 2050 under A2 emission scenario. Areas in which overall decreases are anticipated in crop suitability are shown in green, with increasing color intensity indicating multiple GCM agreement. Areas of declining climatic suitability for restricted range birds are shown in blue, with increasing color intensity indicating multiple GCM agreement. Overlap of declining crop suitability and declining restricted range bird climatic suitability is shown in shades of yellow (lowest GCM agreement) to red (highest GCM agreement).
Global map of crop suitability and suitability for range restricted birds change in 2050/2090 under B1 emission scenario. Areas in which overall decreases are anticipated in crop suitability are shown in green, with increasing color intensity indicating multiple GCM agreement. Areas of declining climatic suitability for restricted range birds are shown in blue, with increasing color intensity indicating multiple GCM agreement. Overlap of declining crop suitability and declining restricted range bird climatic suitability is shown in shades of yellow (lowest GCM agreement) to red (highest GCM agreement).
Global map of crop suitability and suitability for range restricted birds change in 2050/2090 under A2 emission scenario using the ensemble mean of 5 GCMs. Areas in which overall decreases are anticipated in crop suitability are shown in green. Areas of declining climatic suitability for restricted range birds are shown in blue. Overlap of declining crop suitability and declining restricted range bird climatic suitability is shown in red.
Global map of crop suitability and suitability for range restricted birds change in 2050/2090 under B1 emission scenario using mean of 5 GCMs. Areas in which overall decreases are anticipated in crop suitability are shown in green. Areas of declining climatic suitability for restricted range birds are shown in blue. Overlap of declining crop suitability and declining restricted range bird climatic suitability is shown in red.
Global map of crop suitability and suitability for range restricted birds change in 2090 under A2 emission scenario using 6 Species Distribution Model results. Areas in which overall decreases are anticipated in crop suitability are shown in green, with increasing color intensity indicating multiple GCM agreement. Areas of declining climatic suitability for restricted range birds are shown in blue, with increasing color intensity indicating multiple GCM agreement. Overlap of declining crop suitability and declining restricted range bird climatic suitability is shown in shades of yellow (lowest GCM agreement) to red (highest GCM agreement).
We are grateful to Guy Midgley for help and encouragement in the design of the early stages of this project. We thank the many individuals and organizations who contribute to BirdLife’s Red List assessments, including provision of point localities used in the analysis. For helpful comments on an earlier draft we thank M. Heath and E. Perry.
Conceived and designed the experiments: LH MI DH CS ATP SB. Performed the experiments: MI. Analyzed the data: LH MI DH CS ATP SB PR. Contributed reagents/materials/analysis tools: MI SB ATP CS. Wrote the manuscript: LH MI DH CS ATP SB PR.
- 1. IPCC (2007) Climate Change 2007: Impacts, Adaptation and Vulnerability. M. ParryO. CanzianiJ. PalutikofP. van der LindenC. Hanson. Cambridge University Press.
- 2. United Nations Framework Convention on Climate Change (UNFCCC) (2007) Investment and Financial Flows to Address Climate. Change. doi: 10.1590/s1676-06032009000100001
- 3. Bank World (2010) Economics of Adaptation to Climate Change: Synthesis Report.
- 4. Warren R (2011) The role of interactions in a world implementing adaptation and mitigation solutions to climate change. Philos Trans R Soc A 369: 217–241. doi:10.1098/rsta.2010.0271.
- 5. Jones HP, Hole DG, Zavelata ES (2012) Harnessing nature to help people adapt to climate change. Nat Clim Change 2: 504-509. doi:10.1038/nclimate1463.
- 6. Campbell A, Kapos V, Scharlemann JPW, Bubb P, Chenery A et al. (2009) Review of the literature on the links between biodiversity and climate change - impacts, adaptation and mitigation. Montreal: Secretariat of the Convention on Biological Diversity. 124. Field: Lobell DB. p. 7 CB (2007) Global scale climate - crop yield relationships and the impacts of recent warming. Environmental Research Letters. 2. PubMed: 18844221.
- 7. FAO (2007) cocrop. No. 3. Plant Production and Protection Division of FAO 25 FAO Digital Land and Water, Media series. Rome: FAO.
- 8. Palmer MA, Lettenmaier DP, Poff NL, Postel SL, Richter B et al. (2009) Climate Change and River Ecosystems: Protection and Adaptation Options. Environ Manag 44: 1053-1068. doi:10.1007/s00267-009-9329-1. PubMed: 19597873.
- 9. Smith P, Gregory PJ, van Vuuren D, Obersteiner M, Havlík P et al. (2010) Competition for land. Philos Trans R Soc Lond B Biol Sci 365: 2941-2957. doi:10.1098/rstb.2010.0127. PubMed: 20713395.
- 10. Cavendish W (2000) Empirical Regularities in the Poverty-Environment Relationship of Rural Households: Evidence from Zimbabwe. World Dev 28: 1979-2003. doi:10.1016/S0305-750X(00)00066-8.
- 11. Niehof A (2004) The significance of diversification for rural livelihood systems. Food Policy 29: 321-338. doi:10.1016/j.foodpol.2004.07.009.
- 12. Seabrook L, McAlpine CA, Bowen ME (2011) Restore, repair or reinvent: Options for sustainable landscapes in a changing climate. Landscape Urban Plan 100: 407-410. doi:10.1016/j.landurbplan.2011.02.015.
- 13. Turner WR, Bradley BA, Estes LD, Hole DG, Oppenheimer M et al. (2010) Climate change: helping nature survive the human response. Conserv Lett 3: 304-312. doi:10.1111/j.1755-263X.2010.00128.x.
- 14. Mooney H, Larigauderie A, Cesario M, Elmquist T, Hoegh-Guldberg O et al. (2009) Biodiversity, climate change, and ecosystem services. Current Opinion Environ Sustainability 1: 46-54. doi:10.1016/j.cosust.2009.07.006.
- 15. Lin BB, Perfecto I, Vandermeer J (2008) Synergies between Agricultural Intensification and Climate Change Could Create Surprising Vulnerabilities for Crops. BioScience 58: 847-854. doi:10.1641/B580911.
- 16. Hertel TW, Rosch SD (2010) Climate Change, Agriculture, and Poverty. Appl Econ Perspectives Policy 32: 355-385. doi:10.1093/aepp/ppq016.
- 17. Morton JF (2007) The impact of climate change on smallholder and subsistence agriculture. Proc Natl Acad Sci U S A 104: 19680-19685. doi:10.1073/pnas.0701855104. PubMed: 18077400.
- 18. Tewksbury JJ, Huey RB, Deutsch CA (2008) Ecology - Putting the heat on tropical animals. Science 320: 1296-1297. doi:10.1126/science.1159328. PubMed: 18535231.
- 19. Sinervo B, Méndez-de-la-Cruz F, Miles DB, Heulin B, Bastiaans E et al. (2010) Erosion of Lizard Diversity by Climate Change and Altered Thermal Niches. Science 328: 894-899. doi:10.1126/science.1184695. PubMed: 20466932.
- 20. Gornall J, Betts R, Burke E, Clark R, Camp J et al. (2010) Implications of climate change for agricultural productivity in the early twenty-first century. Philos Trans R Soc Lond B Biol Sci 365: 2973-2989. doi:10.1098/rstb.2010.0158. PubMed: 20713397.
- 21. O’Neill BC, Oppenheimer M (2002) Climate Change: Dangerous Climate Impacts and the Kyoto Protocol. Science 296: 1971-1972. doi:10.1126/science.1071238. PubMed: 12065820.
- 22. Lobell DB, Burke MB, Tebaldi C, Mastrandrea MD, Falcon WP et al. (2008) Prioritizing climate change adaptation needs for food security in 2030. Science 319: 607-610. doi:10.1126/science.1152339. PubMed: 18239122.
- 23. Myers N, Mittermeier RA, Mittermeier CG, da Fonesca GAB, Kent J (2000) Biodiversity hotspots for conservation priorities. Nature 403: 853-858. doi:10.1038/35002501. PubMed: 10706275.
- 24. Long AJ, Crosby MJ, Stattersfield AJ (1996) Towards a Global Map of Biodiversity: Patterns in the Distribution of Restricted-Range Birds. Glob Ecol Biogeogr Lett 5: 281-304. doi:10.2307/2997796.
- 25. Stattersfield AJ, Crosby MJ, Long AJ, Wege DC (1998) Endemic Bird Areas of the World - Priorities for Biodiversity Conservation; D. Brooks. Cambridge: BirdLife International. pp. 1-846.
- 26. Sekercioglu CH, Schneider SH, Fay JP, Loarie SR (2008) Climate Change, Elevational. Range Shifts And Birds Extinctions Conserv Biol 22(1): 140-150. doi: 10.1111/j.1523-1739.2007.00852.x
- 27. Elith J, Graham CH, Anderson RP, Dudik M, Ferrier S et al. (2006) Novel methods improve prediction of species’ distributions from occurrence data. Ecography 29: 129-151. doi:10.1111/j.2006.0906-7590.04596.x.
- 28. Phillips SJ, Dudík M, Schapire RE (2004) A maximum entropy approach to species distribution modeling. Proceedings of the Twenty-First International Conference on Machine Learning. pp. 655-662.
- 29. Hastie TJ, Tibshirani R (1990) Generalized additive models London. Chapman and Hall.
- 30. Friedman JH (2001) Greedy function approximation: A gradient boosting machine. Ann Statist 29: 1189-1232. doi:10.1214/aos/1013203451.
- 31. McCullagh P, Nelder JA (1989) Generalized linear models. London: Chapman and Hall.
- 32. Friedman J (1991) Multivariate Additive Regression Splines. Ann Statist 19: 1-67. doi:10.1214/aos/1176347963.
- 33. Breiman L (2001) Random Forests. Machine Learn 45: 5-32. doi:10.1023/A:1010933404324.
- 34. Thuiller W, Lafourcade B, Engler R, Araújo MB (2009) BIOMOD-A platform for ensemble forecasting of species distributions. Ecography 32: 369-373. doi:10.1111/j.1600-0587.2008.05742.x.
- 35. Cohen J (1960) A coefficient of agreement for nominal scales. Educ Psychol Meas 20: 37–46. doi:10.1177/001316446002000104.
- 36. Allouche O, Tsoar A, Kadmon R (2006) Assessing the accuracy of species distribution models: prevalence, kappa and the true skill statistic (TSS). J Appl Ecol 43: 1223-1232. doi:10.1111/j.1365-2664.2006.01214.x.
- 37. Matthews BW (1975) Comparison of the predicted and observed secondary structure of T4 phage lysozyme. Biochim Biophys Acta 405: 442–451. doi:10.1016/0005-2795(75)90109-9. PubMed: 1180967.
- 38. You L, Guo Z, Koo J, Ojo W, Sebastian K, Tenorio MT, Wood S, Wood-Sichra U (2000) Spatial Produciton Allocation Model (SPAM), version 3; Release 1. http://MapSPAM.info.
- 39. Jarvis A, Lane A (2007) Changes in Climate will modify the Geography of Crop Suitability: Agricultural Biodiversity can help with Adaptation. J Semiarid Trop Agric Res 4: 1-12.
- 40. Leakey ADB, Ainsworth EA, Bernacchi CJ, Rogers A, Long SP et al. (2009) Elevated CO2 effects on plant carbon, nitrogen, and water relations: six important lessons from FACE. J Exp Bot 60: 2859-2876. doi:10.1093/jxb/erp096. PubMed: 19401412.
- 41. IPCC (2007) IPCC Fourth Assessment Report: Climate Change 2007 (AR4). Cambridge Cambridge University Press.
- 42. Tabor K, Williams JW (2010) Globally downscaled climate projections for assessing the conservation impacts of climate change. Ecol Appl 20: 554-565. doi:10.1890/09-0173.1. PubMed: 20405806.
- 43. Araújo MB, New M (2007) Ensemble forecasting of species distributions. Trends Ecol Evol 22: 42-47. doi:10.1016/j.tree.2006.09.010. PubMed: 17011070.
- 44. Rosenzweig C, Casassa G, Karoly DJ, Imeson A, Liu C et al. (2007) Assessment of Observed Changes and Responses in Natural and Managed Systems. In: M.L. Parry, Canziani OF, Palutikof JP, Linden PJvd, Hanson CE, editors. Climate change 2007: impacts, adaptation and vulnerability: contribution of Working Group II to the fourth assessment report of Cambridge: The Intergovernmental Panel on Climate Change: Cambridge University Press. pp. 79-131.
- 45. Parry M, Lowe J, Hanson C (2009) Overshoot, adapt and recover. Nature 458: 1102-1103. doi:10.1038/4581102a. PubMed: 19407775.
- 46. Fischer G, van Velthuizen H, Shah M, Nachtergaele F (2002) Global Agro-ecological Assessment for Agriculture in the 21st Century: Methodology and Results. Austria: Laxenburg.
- 47. Shoo LP, Williams SE, Hero J-M (2005) Climate warming and the rainforest birds of the Australian Wet Tropics: Using abundance data as a sensitive predictor of change in total population size. Biol Conserv 125: 335-343. doi:10.1016/j.biocon.2005.04.003.
- 48. Jetz W, Wilcove DS, Dobson AP (2007) Projected impacts of climate and land-use change on the global diversity of birds. PLOS Biol 5: 1211-1219. PubMed: 17550306.
- 49. Malcolm JR, Liu CR, Neilson RP, Hansen L, Hannah L (2006) Global warming and extinctions of endemic species from biodiversity hotspots. Conserv Biol 20: 538-548. doi:10.1111/j.1523-1739.2006.00364.x. PubMed: 16903114.
- 50. Oppenheimer M (1989) Climate Change and Environmental Pollution Physical and Biological Interactions. Clim Change 15: 255-270. doi:10.1007/BF00138854.
- 51. Liverman D, Billett S (2010) Copenhagen and the Governance of Adaptation. Environment Science Policy Sustainable Dev 52: 28-36. doi:10.1080/00139151003761579.
- 52. Phalan B, Onial M, Balmford A, Green RE (2011) Reconciling Food Production and Biodiversity Conservation: Land Sharing and Land Sparing Compared. Science 333: 1289-1291. doi:10.1126/science.1208742. PubMed: 21885781.
- 53. International Food Policy Research Institute (2010) Global Hunger Index 2010 Data. Available: http://www.ifpri.org/sites/default/files/ghi2010data.xlsx.
- 54. Center for International Earth Science Information Network (CIESIN) (2011) /Columbia University, International Food Policy Research Institute (IFPRI), The World Bank and Centro Internacional de Agricultura Tropical (CIAT) . Global Rural-Urban Mapping Project, Version 1 (GRUMPv1): Population Count Grid. Palisades, NY: National Astronautics and Space Administration ; Data Socioeconomic, Applications Center (SEDAC). http://sedac.ciesin.columbia.edu/data/set/grump-v1-population-count. Accessed 11 June 2011.