Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-23T18:02:54.311Z Has data issue: false hasContentIssue false

What are the roles of species distribution models in conservation planning?

Published online by Cambridge University Press:  14 January 2014

WILLIAM J. McSHEA*
Affiliation:
Conservation Ecology Center, Conservation Biology Institute, Smithsonian's National Zoological Park, 1500 Remount Road, Front Royal, VA 22630, USA, e-mail: [email protected]
Rights & Permissions [Opens in a new window]

Extract

The development of species distribution models (SDMs) has benefited biodiversity conservation through their linkage of science to policy and decision processes. These models have evolved to provide scenarios of future landscapes based on known and projected environmental parameters. Whereas there are many caveats to their use, the persuasive power of the models for conveying the consequences of environmental change to the non-science community is immense. Scientists are obliged to convey the uncertainty of the futures depicted in their models, but also to involve the stakeholders who will shape those future conditions. Stakeholders can identify the natural resources they want to sustain, voice their priorities in environmental policy, and articulate the range of solutions they are willing to accept. The creation of alternative futures is an academic exercise if not linked to real viable decisions concerning important resources. SDMs only reach their full potential when they bring together scientists, public stakeholders and policy makers, and are used as an adaptive management tool to understand complex landscapes that are undergoing short- and long-term change.

Type
Editorial
Copyright
Copyright © Foundation for Environmental Conservation 2014 

The development of species distribution models (SDMs) has benefited biodiversity conservation through their linkage of science to policy and decision processes. These models have evolved to provide scenarios of future landscapes based on known and projected environmental parameters. Whereas there are many caveats to their use, the persuasive power of the models for conveying the consequences of environmental change to the non-science community is immense. Scientists are obliged to convey the uncertainty of the futures depicted in their models, but also to involve the stakeholders who will shape those future conditions. Stakeholders can identify the natural resources they want to sustain, voice their priorities in environmental policy, and articulate the range of solutions they are willing to accept. The creation of alternative futures is an academic exercise if not linked to real viable decisions concerning important resources. SDMs only reach their full potential when they bring together scientists, public stakeholders and policy makers, and are used as an adaptive management tool to understand complex landscapes that are undergoing short- and long-term change.

Excellent reviews of the evolution of SDMs exist, and all aspects of the models will not be covered here (Guisan & Thuiller Reference Guisan and Thuiller2005; Elith & Leatherwick Reference Elith and Leathwick2009; Franklin Reference Franklin2009, Reference Franklin2010; Iverson et al. Reference Iverson, Prasad, Matthews and Peters2011). The major points are that distribution models for single or multiple species are created based on survey data across a range of environmental variables. The process identifies critical environmental variables for each species or community, and then extrapolates from the known survey locations to the entire target landscape. These static models either display the predicted distribution as a binary function or as a probability landscape. SDMs can isolate variability due to imperfect detection of species from parameters shaping the species distribution. SDMs have been used to identify suitable habitat for cryptic species (Wilting et al. Reference Wilting, Cord, Hearn, Hesse, Mohamed, Traehold, Cheryne, Sunarto, Jayaslin, Ross, Shapiro, Sebastian, Dech, Breitenmoser, Sanderson, Duckworth and Hofer2010), or for species distributed across broad and/or difficult landscapes that preclude detailed surveys (McShea et al. Reference McShea, Stewart, Peterson, Erb, Stuebing and Giman2009; Liu et al. Reference Liu, McShea, Garshelis, Zhu, Wang, Gong and Chen2009). There is the caveat that mapping potential habitat should not be inferred to represent the actual presence of the species (Guisan & Thuiller Reference Guisan and Thuiller2005). For example, tropical wildlife are experiencing significant poaching pressure within forest reserves (Harrison Reference Harrison2011), and maps of suitable forest may not reflect the abundance of animals within that forest. An additional important limitation is that SDMs assume the surveys are detecting species across their potential range and that important environmental variables (including species interactions) have been considered in the model construction. For species currently confined to refugia, or which are so rare that they occupy only a small portion of their suitable habitat, the resulting distribution model does not reflect the true potential extent of the species and thus exaggerates the lack of potential habitat (Sinclair et al. Reference Sinclair, White and Newell2010; De Ornellas et al. Reference De Ornellas, Milner-Gulland and Nicholson2011). Despite these limitations, SDMs have advanced conservation efforts by allowing conservation planning for the current distribution of many critical species, such as large carnivores in North America (Carroll et al. Reference Carroll, Noss and Paquet2001) and Europe (Corsi et al. Reference Corsi, Duprè and Boitani1999), and riverine fish communities in Mesoamerica (Esselman & Allan Reference Esselman and Allan2011).

Once adopted by the conservation community, static SDMs were almost immediately used to project shifts in distribution into the future due to changes in climate parameters or land-use activities (Guillan & Thuiller Reference Guisan and Thuiller2005). By using parameters that are either directly or indirectly linked to recently available world climate data (Hijmans et al. Reference Hijmans, Cameron, Parra, Jones and Jarvis2005), conservationists have employed SDMs to predict future landscapes (Pereira et al. Reference Pereira, Leadley, Proença, Alkemade, Scharlemann, Fernandez-Manjarrés, Araújo, Balvanera, Biggs, Cheung, Chini, Cooper, Gilman, Guénette, Hurtt, Huntington, Mace, Oberdorff, Revenga, Rodrigues, Scholes, Sumaila and Walpole2010). SDMs have identified corridors between protected areas that would allow movement across temperature gradients (Nuñez et al. Reference Nuñez, Lawler, McRae, Pierce, Krosby, Kavanagh, Singleton and Tewksbury2013), determined functional redundancy in protected area establishment (Gallagher et al. Reference Gallagher, Hughes and Leishman2013), linked key demographic metrics with global change models and prioritized critical habitats (Bonnot et al. Reference Bonnot, Thompson and Millspaugh2011), and allowed planning for increased frequency of extreme weather events in order to conserve an endangered species (Bateman et al. Reference Bateman, VanDerWal and Johnson2012). With effective conservation planning focused on insuring redundancy and resiliency for sustainable future populations (Redford et al. Reference Redford, Amato, Baillie, Beldomenico, Bennett, Clum, Cook, Fonseca, Hedges, Launay, Lieberman, Mace, Murayama, Putnam, Robinson, Rosenbaum, Sanderson, Stuart, Thomas and Thorbjarnarson2011), SDMs are a valuable tool to the conservation community.

This projection of SDMs into a contentious political arena has generated critical review on how the models are constructed and used to predict alternative futures. It is these future projections that have drawn the most criticism of SDMs, primarily because of inherent variability of the environmental parameters, the unknown migration ability of the species, and model uncertainty, which are not always incorporated into the predictions (Cayuela et al. Reference Cayuela, Golicher, Newton, Kolb, de Alburquerque, Arets, Alkemade and Pérez2009; Coreau et al. Reference Coreau, Pinay, Thompson, Cheptou and Mermet2009; Elith & Leatherwick Reference Elith and Leathwick2009; Franklin Reference Franklin2010; Sinclair et al. Reference Sinclair, White and Newell2010). Many of the same limits to static SDMs are at issue when linking SDMs to climate models. For example, the scale of a species’ environmental niche is often small relative to outputs of climate models and undetected climate refugia will exist within these future landscapes (Weins & Bachelet Reference Weins and Bachelet2010). In addition, anthropogenic stresses may have complex interactions with projected changes in climate parameters (Singh & Milner-Gulland Reference Singh and Milner-Gulland2011) and the uncertainty values of critical parameters makes future predictions challenging for some species (Carvalho et al. Reference Carvalho, Brito, Crespo, Watts and Possingham2011). Of particular note is that the persistence of organisms in future landscapes depends partially on their ability to migrate into newly suitable habitats, abilities that are poorly understood for most species (Franklin Reference Franklin2009, Reference Franklin2010).

These issues demand constant vigilance when selecting focal species and landscapes, but they are tractable with the development of new techniques and a critical scientific community. Of primary concern is that this predictive modelling often places species in future communities that do not exist at present, or into a parameter space not encompassed by the original SDMs (Coreau et al. Reference Coreau, Pinay, Thompson, Cheptou and Mermet2009). Although most SDMs focus on single species, as the modelling environment approaches unique combinations of parameters, there is increased uncertainty over the interactions with other species and between the environmental variables, which can make predictions problematic (Carvalho et al. Reference Carvalho, Brito, Crespo, Watts and Possingham2011). For broad-ranging species that occur across diverse and varied landscapes these conditions may never be reached, but for specialist (or rare) species caution is advisable before mapping future distributions.

SDMs linked to future landscapes are most credible when focused on well-studied species within systems where the important parameters are understood. Temperate forest communities are an excellent example where SDMs are linked to climate models to project future communities. Due in part to their large economic value, scientists have a better understanding of the physiology, species interactions and dispersal capabilities of temperate tree species than any other ecosystem (possibly temperate freshwater systems come close). Several successful SDMs have created future projections for forest (Iverson et al. Reference Iverson, Prasad, Matthews and Peters2011; Thompson et al. Reference Thompson, Foster, Scheller and Kittredge2011), lake (Peterson et al. Reference Peterson, Cumming and Carpenter2003) or riverine (Esselman & Allan Reference Esselman and Allan2011; Turak et al. Reference Turak, Ferrier, Barrett, Mesley, Driesma, Manion, Doyle, Stein and Gordon2011) communities. The challenge is to bring together the same level of knowledge when modelling other important communities, such as tropical forests or marine communities. The next difficult step is linking forest communities, which can be mapped remotely at broad scales, with animal communities, which are often loosely correlated to forest distributions and are often incompletely mapped at a much smaller scale. There are few animal communities understood to the degree that the distribution and extent of forest communities can serve as a surrogate for SDM purposes (Faaborg et al. Reference Faaborg, Holmes, Anders, Bildstein, Dugger, Gauthreaux, Heglund, Hobson, Jahn, Johnson, Latta, Levey, Marra, Merkord, Nol, Rothstein, Sherry, Sillett, Thompson and Warnock2010).

Modelling limitations should not dissuade conservationists from using the predictive power of SDMs. A dynamic SDM, based on well-surveyed populations responding to changes in known-critical parameters, is one of the best tools available for conservationists to visually convey future conditions. Users should be aware of limitations, but the model insights are an important starting point for decision making (Carvalho et al. Reference Carvalho, Brito, Crespo, Watts and Possingham2011). It may be unknown which projection best reflects reality 100 years in the future, but presenting a range of possible outcomes to stakeholders may trigger action today. Scenario planning is a good example of how a SDM can be effectively used for conservation planning (Coreau et al. Reference Coreau, Pinay, Thompson, Cheptou and Mermet2009; Foster et al. Reference Foster, Donohue, Kitteredge, Lambert, Hunter, Hall, Irland, Liliehom, Orwig, D'Amaot, Colburn, Thompson, Levitt, Ellison, Keeton, Aber, Cogbill, Driscoll, Fahey and Hart2010; Periera et al. Reference Pereira, Leadley, Proença, Alkemade, Scharlemann, Fernandez-Manjarrés, Araújo, Balvanera, Biggs, Cheung, Chini, Cooper, Gilman, Guénette, Hurtt, Huntington, Mace, Oberdorff, Revenga, Rodrigues, Scholes, Sumaila and Walpole2010; Thompson et al. Reference Thompson, Wiek, Swanson, Carpenter, Fresco, Hollingsworth, Spies and Foster2012). With scenario planning, alternative futures are presented to stakeholders based on the policy actions available to them. This has been tried at regional (Spies et al. Reference Spies, Johnson, Burnett, Ohmann, McComb, Reeves, Bettinger, Kline and Garber-Younts2007; Shaw Reference Shaw, Sheppard, Burch, Flanders, Wiek, Carmichael, Robinson and Cohen2009; Foster et al. Reference Foster, Donohue, Kitteredge, Lambert, Hunter, Hall, Irland, Liliehom, Orwig, D'Amaot, Colburn, Thompson, Levitt, Ellison, Keeton, Aber, Cogbill, Driscoll, Fahey and Hart2010) and global (Millennium Ecosystem Assessment 2005; Periera et al. Reference Pereira, Leadley, Proença, Alkemade, Scharlemann, Fernandez-Manjarrés, Araújo, Balvanera, Biggs, Cheung, Chini, Cooper, Gilman, Guénette, Hurtt, Huntington, Mace, Oberdorff, Revenga, Rodrigues, Scholes, Sumaila and Walpole2010) scales. In my opinion, the regional efforts have been successful at conveying policy impacts on environmental services.

For the conservation community focused on endangered species, these future SDMs are analogous to population habitat viability analysis (PHVA), where population parameters are used to determine the current population growth rate and then are projected into future generations in the presence of known stressors (Akçakaya & Sjögren-Gulve Reference Akçakaya and Sjögren-Gulve2000; Linkie et al. Reference Linkie, Chapron, Martyr, Holden and Leader-Williams2006; Redford et al. Reference Redford, Amato, Baillie, Beldomenico, Bennett, Clum, Cook, Fonseca, Hedges, Launay, Lieberman, Mace, Murayama, Putnam, Robinson, Rosenbaum, Sanderson, Stuart, Thomas and Thorbjarnarson2011). PHVA workshops for stakeholders then explore the minimum and maximum levels for each stressor that allow population persistence over the projected time span. The stakeholder process strives to recognize and accept the limits within which land and animal usage will allow persistence of the target population. PHVAs have been incorporated into a metapopulation schema, where sources and sinks for populations are temporally and spatially variable due to shifting resources (Bonnot et al. Reference Bonnot, Thompson and Millspaugh2011). This linking of population parameters with environmental change across a landscape holds much potential for SDMs that seek to predict the future viability of critical species (Elith & Leatherwick Reference Elith and Leathwick2009; Franklin Reference Franklin2010).

SDMs can accomplish conservation aims through several avenues:

  1. (1) Many environmental threats are imminent and operate within known parameters. For many species and communities, impacts of forest loss, increased road density and dam construction are understood. Short-term projections of climate models do not bring species outside the parameter limits used for model creation. For many endangered communities, SDMs are of valuable assistance in projecting the short-term consequences of policy decisions.

  2. (2) For some situations it is best to consider these future models not as predictions, but as scenarios. This is with the stipulation that, if known parameters stay within their limits, future landscapes can be projected, based on a limited number of policy decisions. These alternative futures do not make predictions of how likely each future landscape is, but provide a critical tool for stakeholders to discuss how today's decisions shape future landscapes.

  3. (3) Spatial distribution modelling is a rapidly evolving field, with advances in technology for species' detection, modelling software and mathematical theorems, and an understanding of important parameters for an increasing number of species. SDMs should result from an iterative process for the conservation community, with important models revised and re-parametized on a regular basis. As ‘current-state-of-knowledge’, SDMs are one step toward bringing science into policy making.

  4. (4) Hundreds of SDMs exist, from marine to terrestrial systems, yet the science is not well used by the conservation community. This community needs to take a more proactive role in the funding of SDM research. The research community is currently driving most SDM development, and the products are relevant to ecologists (understanding basic population and ecosystem principles) and produce meaningful products within the science community (namely papers for scientific journals and conference presentations). The conservation community often needs different products, such as usable applications and scientific input into policy development. Explicitly creating SDMs for policy development is more likely to produce applications that are useable and used by practitioners, and make better use of visualization tools (McIntyre & Strauss Reference McIntyre and Strauss2013). The development of joint ventures based around ecosystems (Bonnott et al. Reference Bonnot, Thompson and Millspaugh2011) or species (Lynch & Taylor Reference Lynch and Taylor2010), or multi-agency partnerships for migratory bird conservation (Faaborg et al. Reference Faaborg, Holmes, Anders, Bildstein, Dugger, Gauthreaux, Heglund, Hobson, Jahn, Johnson, Latta, Levey, Marra, Merkord, Nol, Rothstein, Sherry, Sillett, Thompson and Warnock2010), is a promising avenue for merging the science and management communities.

  5. (5) The conservation community is not the final user of any SDM. The goal is to link the modelling to policy makers and managers (Euliss et al. Reference Euliss, Smith, Liu, Duffy, Faulkner, Gleason and Eckles2011). There is insufficient effort to convey SDM outputs to decision-makers. Even this volume had limited success in finding research that moved from theory to practice. More research is needed on how to use SDMs in the service of informing public policy, stakeholder scenario analysis and applied conservation (Driscoll et al. Reference Driscoll, Lambert, Chapin, Nowak, Spies, Swanson, Kittredge and Hart2012). The conservation community needs improved understanding of the relative merits of different modelling approaches in terms of their ability to influence policy and management.

The purpose of this thematic issue is to highlight the role of spatial simulation models in informing conservation planning for global change. The issue encompasses specialist organisms that require narrow environmental envelopes, mobile terrestrial species that rely on unrestricted movements across landscapes, and landscape-scale simulation studies that quantify changes in ecosystem services. I encourage the conservation community to embrace a reasoned use of species distribution model throughout the planning process as a means of engaging stakeholders in discussions of future scenarios and the decisions needed to reach their desired outcomes.

References

Akçakaya, H.R. & Sjögren-Gulve, P. (2000) Population viability analyses in conservation planning: an overview. Ecological Bulletins 48: 921.Google Scholar
Bateman, B.L., VanDerWal, J. & Johnson, C.N. (2012) Nice weather for bettongs: using weather events, not climate means, in species distribution models. Ecography 35: 306314.CrossRefGoogle Scholar
Bonnot, T.W., Thompson, F.R. III & Millspaugh, J.J. (2011) Extension of landscape-based population viability models to ecoregional scales for conservation planning. Biological Conservation 144: 20412053.CrossRefGoogle Scholar
Carroll, C., Noss, R.F. & Paquet, P.C. (2001) Carnivores as focal species for conservation planning in the Rocky Mountain region. Ecological Applications 11: 961980.CrossRefGoogle Scholar
Carvalho, S.B., Brito, J.C., Crespo, E.G., Watts, M.E. & Possingham, H.P. (2011) Conservation planning under climate change: toward accounting for uncertainty in predicted species distributions to increase confidence in conservation investments in space and time. Biological Conservation 144: 20202030.CrossRefGoogle Scholar
Cayuela, L, Golicher, D., Newton, A., Kolb, H., de Alburquerque, F.S., Arets, E.J.M.M., Alkemade, J.R.M. & Pérez, A.M. (2009) Species distribution modeling in the tropics: problems, potentialities, and the role of biological data for effective species conservation. Tropical Conservation Science 2: 319352.CrossRefGoogle Scholar
Coreau, A., Pinay, G., Thompson, J.D., Cheptou, P.-O. & Mermet, L. (2009) The rise of research on futures in ecology: rebalancing scenarios and predictions. Ecology Letters 12: 12771286.CrossRefGoogle ScholarPubMed
Corsi, F., Duprè, E. & Boitani, L. (1999) A large-scale model of wolf distribution in Italy for conservation planning. Conservation Biology 13: 150159.CrossRefGoogle Scholar
De Ornellas, P., Milner-Gulland, E.J. & Nicholson, E. (2011) The impact of data realities on conservation planning. Biological Conservation 144: 19801988.CrossRefGoogle Scholar
Driscoll, C.T., Lambert, K.F., Chapin, F.S. III, Nowak, D.J., Spies, T.A., Swanson, F.J., Kittredge, D.B. Jr & Hart, C.M. (2012) Science and society: the role of long-term studies in environmental stewardship. Bioscience 62: 354366.CrossRefGoogle Scholar
Elith, J. & Leathwick, J.R. (2009) Species distribution models: ecological explanation and prediction across space and time. Annual Review Ecology Evolution Systematics 40: 677697.CrossRefGoogle Scholar
Esselman, P.C. & Allan, J.D. (2011) Application of species distribution models and conservation planning software to the design of a reserve network for the riverine fishes of northeastern Mesoamerica. Freshwater Biology 56: 7188.CrossRefGoogle Scholar
Euliss, N.H. Jr, Smith, L.M., Liu, S., Duffy, W.G., Faulkner, S.P., Gleason, R.A. & Eckles, S.D. (2011) Integrating estimates of ecosystem services from conservation programs and practices into models for decision makers. Ecological Applications 21: S128–S134.CrossRefGoogle Scholar
Faaborg, J., Holmes, R.T., Anders, A.D., Bildstein, K.L., Dugger, K.M., Gauthreaux, S.A. Jr, Heglund, P., Hobson, K.A., Jahn, A.E., Johnson, D.H., Latta, S.C., Levey, D.J., Marra, P.P., Merkord, C.L., Nol, E., Rothstein, S.I., Sherry, T.W., Sillett, T.S., Thompson, F.R. III & Warnock, N. (2010) Conserving migratory land birds in the New World: do we know enough? Ecological Applications 20: 398418.CrossRefGoogle Scholar
Franklin, J. (2009) Mapping Species Distributions: Spatial Inference and Prediction. Cambridge, UK: Cambridge University Press.Google Scholar
Franklin, J. (2010) Moving beyond static species distribution models in support of conservation biogeography. Diversity and Distributions 16: 321330.CrossRefGoogle Scholar
Foster, D.R., Donohue, B.M., Kitteredge, D.B., Lambert, K.F., Hunter, M.L., Hall, B.R., Irland, L.C., Liliehom, R.J., Orwig, D.A., D'Amaot, A.W., Colburn, E.A., Thompson, J.R., Levitt, J.N., Ellison, A.M., Keeton, W.S., Aber, J.D., Cogbill, C.V., Driscoll, C.T., Fahey, T.J. & Hart, C.M. (2010) Wildlands and Woodlands: A Vision for the New England Landscape. Petersham, MA, USA: Harvard Forest, Harvard University.Google Scholar
Gallagher, R.V., Hughes, L. & Leishman, M.R. (2013) Species loss and gain in communities under future climate change: consequences for functional diversity. Ecography 36: 531540.CrossRefGoogle Scholar
Guisan, A. & Thuiller, W. (2005) Predicting species distribution: offering more than simple habitat models. Ecology Letters 8: 9931009.CrossRefGoogle ScholarPubMed
Harrison, R.D. (2011) Emptying the forest: hunting and the extirpation of wildlife from tropical nature reserves. Bioscience 61: 919924.CrossRefGoogle Scholar
Hijmans, R.J., Cameron, S.E., Parra, J.L., Jones, P.G. & Jarvis, A. (2005) Very high resolution interpolated climate surfaces for global land areas. International Journal of Climatology 25: 19651978.CrossRefGoogle Scholar
Iverson, L.R., Prasad, A.M., Matthews, S.N. & Peters, M.P. (2011) Lessons learned while integrating habitat, dispersal, disturbance, and life-history traits into species habitat models under climate change. Ecosystems 14: 10051020.CrossRefGoogle Scholar
Linkie, M., Chapron, G., Martyr, D.J., Holden, J. & Leader-Williams, N. (2006) Assessing the viability of tiger subpopulations in a fragmented landscape. Journal of Applied Ecology 43: 576586.CrossRefGoogle Scholar
Liu, F., McShea, W.J., Garshelis, D.L., Zhu, X., Wang, D., Gong, J. & Chen, Y. (2009) Spatial distribution as a measure of conservation needs: an example with Asiatic black bears in Southwestern China. Biodiversity and Distribution 15: 649659.CrossRefGoogle Scholar
Lynch, A.J. & Taylor, W.W. (2010) Evaluating a science-based decision support tool used to prioritize brook charr conservation project proposals in the eastern United States. Hydrobiologia 650: 233241.CrossRefGoogle Scholar
McIntyre, N.E. & Strauss, R.E. (2013) A new multi-scaled graph visualization approach: an example with the playa wetland network in the great plains. Landscape Ecology 28: 769782.CrossRefGoogle Scholar
McShea, W.J., Stewart, C., Peterson, L., Erb, P., Stuebing, R. & Giman, B. (2009) The importance of secondary forest blocks for terrestrial mammals within an Acacia/secondary forest matrix in Sarawak, Malaysia. Biological Conservation 142: 31083119.CrossRefGoogle Scholar
Millennium Ecosystem Assessment (2005) Ecosystems and Human Well-being: Scenarios. Washington, DC, USA: Island Press Google Scholar
Nuñez, T.A., Lawler, J.J., McRae, B.H., Pierce, D.J., Krosby, M.B., Kavanagh, D.M., Singleton, P.H. & Tewksbury, J.J. (2013) Connectivity planning to address climate change. Conservation Biology 27: 407416.CrossRefGoogle ScholarPubMed
Peterson, G.D., Cumming, G.S. & Carpenter, S. (2003) Scenario planning: a tool for conservation in an uncertain world. Conservation Biology 17: 358366.CrossRefGoogle Scholar
Pereira, H.M., Leadley, P.W., Proença, V., Alkemade, R., Scharlemann, J.P.W., Fernandez-Manjarrés, J.F., Araújo, M.B., Balvanera, P., Biggs, R., Cheung, W.W.L., Chini, L., Cooper, H.D., Gilman, E.L., Guénette, S., Hurtt, G.C., Huntington, H.P., Mace, G.M., Oberdorff, T., Revenga, C., Rodrigues, P., Scholes, R.J., Sumaila, U.R. & Walpole, M. (2010) Scenarios for global biodiversity in the 21st century. Science 330: 14961501.CrossRefGoogle Scholar
Redford, K.H., Amato, G., Baillie, J., Beldomenico, P., Bennett, E.L., Clum, N., Cook, R., Fonseca, G., Hedges, S., Launay, F., Lieberman, S., Mace, G.M., Murayama, A., Putnam, A., Robinson, J.G., Rosenbaum, H., Sanderson, E.W., Stuart, S.N., Thomas, P. & Thorbjarnarson, J. (2011) What does it mean to successfully conserve a (vertebrate) species? BioScience 61: 3948.CrossRefGoogle Scholar
Shaw, A., Sheppard, S., Burch, S., Flanders, D., Wiek, A., Carmichael, J., Robinson, J. & Cohen, S. (2009) Making local futures tangible. Synthesizing, downscaling and visualizing climate change scenarios for participatory capacity building. Global Environmental Change 19: 447463.CrossRefGoogle Scholar
Sinclair, S.J., White, M.D. & Newell, G.R. (2010) How useful are species distribution models for managing biodiversity under future climates? Ecology and Society 15: 8 [www document]. URL http://www.ecologyandsociety.org/vol15/iss1/art8/ CrossRefGoogle Scholar
Singh, N.J. & Milner-Gulland, E.J. (2011) Conserving a moving target: planning protection for a migratory species as its distribution changes. Journal of Applied Ecology 48: 3546.CrossRefGoogle Scholar
Spies, T.A., Johnson, K.N., Burnett, K.M., Ohmann, J.L., McComb, B.C., Reeves, G.C., Bettinger, P., Kline, J.D. & Garber-Younts, B. (2007) Cumulative ecological and socioeconomic effects of forest policies in coastal Oregon. Ecological Applications 17: 517.CrossRefGoogle ScholarPubMed
Thompson, J.R., Foster, D.R., Scheller, R. & Kittredge, D. (2011) The influence of land use and climate change on forest biomass and composition in Massachusetts, USA. Ecological Applications 21: 24252444.CrossRefGoogle ScholarPubMed
Thompson, J.R., Wiek, A., Swanson, F.J., Carpenter, S.R., Fresco, N., Hollingsworth, T., Spies, T.A. & Foster, D.A. (2012) Scenario studies as a synthetic and integrative research activity for long-term ecological research. BioScience 62: 367376.CrossRefGoogle Scholar
Turak, E., Ferrier, S., Barrett, T., Mesley, E., Driesma, M., Manion, G., Doyle, G., Stein, J. & Gordon, G. (2011) Planning for the persistence of river biodiversity: exploring alternative futures using process-based models. Freshwater Biology 56: 3956.CrossRefGoogle Scholar
Weins, J.A. & Bachelet, D. (2010) Matching the multiple scales of conservation with the multiple scales of climate change. Conservation Biology 24: 5162.CrossRefGoogle Scholar
Wilting, A., Cord, A., Hearn, A.J., Hesse, D., Mohamed, A., Traehold, C., Cheryne, S.M., Sunarto, S., Jayaslin, M.-A., Ross, J., Shapiro, A.C., Sebastian, A., Dech, S., Breitenmoser, C., Sanderson, J., Duckworth, J.W. & Hofer, H. (2010) Modeling the species distribution of flat-headed cats (Prionailurus planiceps), an endangered south-east Asian small felid. PLoS ONE 5: e9612.CrossRefGoogle ScholarPubMed
Supplementary material: File

McShea Supplementary Material

Supplementary Material

Download McShea Supplementary Material(File)
File 12.3 KB