1 Intraspecific morphological and genetic variation of common species predicts ranges of 2 threatened ones 3 Electronic Supplementary Material 4 5 (a) Inclusion of cost into the prioritizations 6 Land value is typically an extremely important factor in the establishment of areas to conserve 7 biodiversity. Indeed, historically, conservation areas have often been decreed in inexpensive land 8 that was considered unsuitable for development such as areas that are steep or otherwise 9 physically inaccessible [1,2]. Furthermore, since there is significant spatial variation in land cost 10 at the global scale and the national scale [3,4], when cost is incorporated into the prioritization of 11 conservation areas, the portfolio of selected sites can differ significantly from prioritizations that 12 fail to account for cost. To address this, we repeated the analysis incorporating land cost to assess 13 whether sites prioritized to include genetic and morphological variation of common species and 14 minimize land cost would include more habitat for threatened and endemic species than sites 15 selected to minimize land cost and include environmental parameters or occurrences of bird and 16 amphibian species. 17 Since there is no database of land values for Ecuador, we modeled land value as an 18 increasing function of proximity to roads and infrastructure and a decreasing function of site 19 steepness [5,6]. Our land cost model was defined as follows: Sets 𝑖∈𝐼 10 × 10 km sites Data 1 𝑡𝑖 topographic diversity of site 𝑖 𝑟𝑖 number of transformed pixels in 𝑖 𝑑𝑖 distance from 𝑖 to the closest road 20 A site’s topographic diversity is defined as the surface area divided by the planimetric area [5]. 21 Steep, physically-inaccessible sites have high topographic diversity and flat sites that are suitable 22 for development have low topographic diversity. We calculated topographic diversity by 23 obtaining a digital elevation model for the study region [7] and then calculating the surface area 24 of each site using 3D Analyst Tools in ArcGIS 10. We assumed that flatter sites are more 25 desirable and expensive than steep sites. The number of “transformed” pixels per site is an 26 estimate of the amount of infrastructure and anthropogenic activity at a site. Transformed pixels 27 include artificial surfaces such as urban areas and farmland and were obtained from a satellite- 28 derived land cover map [8]. We assumed that transformed, urbanized land was more valuable 29 than land lacking infrastructure. Major roads were obtained from a GIS database [9]. Our model 30 makes the assumption that sites close to the road network are more valuable than remote sites 31 distant from roads. To model the idea that flat, developed sites located near the road network are 32 more expensive that steep, undeveloped sites distant from roads, we defined site cost as: 𝑐𝑖 = 2 1 𝑟𝑖 𝑡𝑖 𝑑𝑖 + (𝑚𝑎𝑥 − (𝑚𝑎𝑥 + 𝑚𝑎𝑥 )) 3 3 𝑖∈𝐼 𝑟𝑖 𝑡 𝑑 𝑖∈𝐼 𝑖 𝑖∈𝐼 𝑖 33 Distance from roads is measured in units of meters whereas topographic diversity is in units of 34 m3 and the number of transformed pixels is dimensionless. So that each term would contribute 35 equally to the site cost, we normalized the terms by dividing by the maximum value in the study 36 region such that road distance, transformed pixels, and topographic diversity each have a 37 maximum value of one. The above cost definition also rescales the sum of road distance, 2 38 transformed pixels, and topographic diversity cost such that flat, developed land close to roads 39 has a cost of one and steep, undeveloped land far from roads has a cost of zero. 40 41 Next, we prioritized sites to meet two criteria: (i) include 17% of the land containing genetic and 42 morphological traits of common species and (ii) minimize land cost as defined above. Sites were 43 selected using the “Multi-criteria minimum area problem” option in the ConsNet 2.0 software 44 package [10]. We also prioritized sites to include environmental parameters and occurrences of 45 amphibian and bird species while minimizing site cost. Results indicate that when cost is 46 included in the analysis, genetic and morphological traits of seven common species remain the 47 best surrogate for threatened and endemic species (figure S3). To begin, in figure S3, the line 48 representing genetic and morphological traits is above and to the left of the line that represents 49 sites selected at random for almost all data points. This means that intraspecific variation almost 50 always performs significantly better than random with respect to the representation of threatened 51 and endemic species. Furthermore, genetic and morphological traits perform better than 52 environmental parameters or occurrences of amphibian and bird species when land value is 53 included in the prioritization. In figure S3, the lines representing species occurrences and 54 environmental parameters are below and to the right of the line that represents randomly selected 55 sites for more than half of the data points, indicating that bird and amphibian occurrences and 56 environmental data perform no better than random in the majority of cases. Finally, the line that 57 depicts genetic and morphological traits is always above and to the left of the lines representing 58 species occurrences and environmental variables, which means that areas prioritized based on 59 genetic and morphological data include more habitat for threatened and endemic species than 3 60 sites prioritized based on occurrences of amphibians and birds or environmental data when the 61 prioritization accounts for land cost. 62 4 63 References 64 65 1. Pressey, R. L., Humphries, C. J., Margules, C. R., Vanewright, R. I. & Williams, P. H. 1993 66 Beyond opportunism - key principles for systematic reserve selection. Trends in Ecology 67 & Evolution 8, 124-128. 68 2. Cantu, C., Wright, R. G., Scott, J. M. & Strand, E. 2004 Assessment of current and proposed 69 nature reserves of Mexico based on their capacity to protect geophysical features and 70 biodiversity. Biological Conservation 115, 411-417. 71 3. Bode, M., Wilson, K. A., Brooks, T. M., Turner, W. R., Mittermeier, R. A., McBride, M. F., 72 Underwood, E. C. & Possingham, H. P. 2008 Cost-effective global conservation 73 spending is robust to taxonomic group. Proc Natl Acad Sci U S A 105, 6498-6501. 74 75 76 4. Ando, A., Camm, J., Polasky, S. & Solow, A. 1998 Species distributions, land values, and efficient conservation. Science 279, 2126-2128. 5. Osano, P. M., Rouget, M., Turpie, J., Thuiller, W. & Balmford, A. 2011 Estimating Land 77 Prices and Opportunity Costs of Conservation in a Megadiversity Country. In African 78 Technology Policy Studies Network Working Papers Series, vol. 58. Nairobi: ATPS. 79 6. Azar, K. T., Ferreira, J., Jr., Abed, J. & Kazzaz, T. 1994 Using GIS for estimating the spatial 80 distribution of land value in metropolitan Beirut. URISA Proceedings Papers from the 81 Annual Conference of the Urban and Regional Information Systems Association 82 Integrating Information and Technology: IT Makes Sense, 805-20 vol.120 vol.1. 5 83 7. Farr, T. G., Rosen, P. A., Caro, E., Crippen, R., Duren, R., Hensley, S., Kobrick, M., Paller, 84 M., Rodriguez, E., Roth, L., et al. 2007 The shuttle radar topography mission. Reviews of 85 Geophysics 45. 86 87 88 89 8. Arino, O., Bicheron, P., Achard, F., Latham, J., Witt, R. & Weber, J.-L. 2008 GlobCover: the most detailed portrait of Earth. Eur Space Ag Bull 136, 25-31. 9. Environmental Systems Research Institute. 2012 ESRI Data & Maps and Streetmap North America for ArcGIS 10.1. Redlands, California: ESRI. 90 10. Ciarleglio, M., Barnes, J. W. & Sarkar, S. 2009 ConsNet: new software for the selection of 91 conservation area networks with spatial and multi-criteria analyses. Ecography 32, 205- 92 209. 93 11. Sarkar, S., Justus, J., Fuller, T., Kelley, C., Garson, J. & Mayfield, M. 2005 Effectiveness of 94 environmental surrogates for the selection of conservation area networks. Conserv Biol 95 19, 815-825. 96 97 98 99 12. Syrjala, S. E. 1996 A statistical test for a difference between the spatial distributions of two populations. Ecology 77, 75-80. 13. Thomassen, H. A., Fuller, T., Buermann, W., Mila, B., Kieswetter, C. M., Jarrin-V., P., Cameron, S. E., Mason, E., Schweizer, R., Schlunegger, J., et al. 2011 Mapping 100 evolutionary process: a multi-taxa approach to conservation prioritization. Evol App 4, 101 397-413. 6 102 14. Peralvo, M., Sierra, R., Young, K. R. & Ulloa-Ulloa, C. 2007 Identification of biodiversity 103 conservation priorities using predictive modeling: an application for the Equatorial 104 Pacific region of South America. Biodivers Conserv 16, 2649-2675. 105 15. Hijmans, R. J., Cameron, S. E., Parra, J. L., Jones, P. G. & Jarvis, A. 2005 Very high 106 resolution interpolated climate surfaces for global land areas. International Journal of 107 Climatology 25, 1965-1978. 108 109 110 16. Batjes, N. H. 1997 A world dataset of derived soil properties by FAO-UNESCO soil unit for global modelling. Soil Use and Management 13, 9-16. 17. Sarkar, S., Mayfield, M., Cameron, S., Fuller, T. & Garson, J. 2007 Conservation area 111 networks for the Indian region: systematic methods and future prospects. Himalayan 112 Journal of Sciences 4, 27-40. 113 18. Sarkar, S., Fuller, T., Aggarwal, A., Moffett, A. & Kelley, C. 2009 The ConsNet software 114 platform for systematic conservation planning. In Spatial Conservation Prioritization: 115 Quantitative Methods and Computational Tools (ed. A. Moilanen, K. A. Wilson & H. P. 116 Possingham), pp. 235-248. New York: Oxford University Press. 117 19. Sarakinos, H., Nicholls, A. O., Tubert, A., Aggarwal, A., Margules, C. R. & Sarkar, S. 2001 118 Area prioritization for biodiversity conservation in Quebec on the basis of species 119 distributions: a preliminary analysis. Biodivers Conserv 10, 1419-1472. 7 120 20. Illoldi-Rangel, P., Fuller, T., Linaje, M., Pappas, C., Sanchez-Cordero, V. & Sarkar, S. 2008 121 Solving the maximum representation problem to prioritize areas for the conservation of 122 terrestrial mammals at risk in Oaxaca. Diversity and Distributions 14, 493-508. 123 21. Fuller, T., Munguia, M., Mayfield, M., Sanchez-Cordero, V. & Sarkar, S. 2006 Incorporating 124 connectivity into conservation planning: A multi-criteria case study from central Mexico. 125 Biological Conservation 133, 131-142. 126 22. Fuller, T., Sanchez-Cordero, V., Illoldi-Rangel, P., Linaje, M. & Sarkar, S. 2007 The cost of 127 postponing biodiversity conservation in Mexico. Biological Conservation 134, 593-600. 128 23. International Union for the Conservation of Nature. 1994 World Conservation Strategy: 129 Conservation for Sustainable Development. Gland, Switzerland: Worldwide Fund for 130 Nature. 131 132 133 134 8 135 Table captions 136 Table S1. Spatial resolution of the planning units for the selection of conservation areas, 137 generalized dissimilarity models (GDMs) of genetic and morphological diversity, and 138 species distribution models (SDMs) for threatened and endemic species. At all spatial 139 resolutions, the analysis utilized square cells. 140 Table S2. Spatial congruence of conservation areas selected to include genetic and 141 morphological traits of common species and threatened and endemic species. The spatial 142 configurations of sites prioritized to include intraspecific variation were compared to 143 configurations of areas prioritized based on threatened and endemic species using a Cramer-von 144 Mises test [11,12]. The null hypothesis is that there is significant overlap in the spatial 145 configurations of the selected areas. In each case, we failed to reject the null hypothesis, 146 suggesting that areas priorized based on genetic and morphological variation are similar in 147 spatial extent to land selected based on threatened and endemic species. 148 Table S3. Environmental classes used in the surrogacy analysis. 9 149 Table S1. Planning unit Selection of conservation areas and surrogacy analysis Scale (km) 10 No. of planning units 639 GDM 1 9378 GDM predicts the distribution of environmentallyassociated genetic and morphological variation across the landscape. The environmental variables were available at the 1 km scale [13]. SDM 1 9378 Environmental variables used to construct the species distribution models were available at the 1 km resolution [14]. 150 10 Rationale The correlation between surrogates and threatened species is highest at this scale [11]. 151 Table S2. Target for genetic and morphological traits (%) 10 10 10 17 17 17 Target for threatened & endemic species (%) 17 34 50 17 34 50 Cramer-von Mises statistic 1.557 2.336 2.899 2.103 2.624 3.273 152 11 p 0.81 1 1 0.5 1 1 153 Table S3. Environmental variable(s) Annual mean temperature, total annual precipitation Aspect Elevation Maximum temperature of the hottest quarter of the year, minimum temperature of the coldest quarter Slope Reference [15] Data Processing* Divided into 10 equal interval classes Calculated from elevation** [7] [15] Divided into nine classes of 40° each Divided into 10 equal interval classes Divided into four equal interval classes Calculated from elevation** Soil type [16] Divided into five classes based on standard deviations Utilized soil associations types in the FAO world soil map 154 *Processing of environmental variables follows published protocols [11,17]. 155 **Aspect and slope were calculated from elevation using Spatial Analyst Tools in ArcGIS 10. 156 12 157 Figure captions 158 Figure S1. Workflow for converting genetic and morphological variation into a set of 159 prioritized areas. 160 161 Figure S2. Bar heights represent the number of threatened and endangered species per 100 162 km2 site when sites were prioritized based on: (a) genetic and morphological variation of 163 seven common species, (b) environmental features, and (c) species occurrences. In each 164 panel, the vertical axis is richness of threatened and endemic species. Sites prioritized based on 165 genetic and morphological diversity of common species contain more threatened and endemic 166 species per site than sites prioritized based on environmental features or occurrences of birds and 167 amphibians. The mean number of threatened and endangered species in the entire set of the 168 selected sites is also highest when we prioritized areas based on intraspecific genetic and 169 morphological variation (figure 2 of the main text). Bars are normalized by the mean richness of 170 threatened and endemic species in each panel. 171 172 Figure S3. Effectiveness of genetic and morphological surrogates for threatened and 173 endemic species when land cost is included in the prioritizations. 174 175 Figure S4. Sites selected to include genetic and morphological traits are effective surrogates 176 for threatened and endemic species when we used lower percentage targets for the former 177 and higher percentage targets for the latter than in the main text. (A) The targets for the 178 selection of sites: 50% for threatened and endemic species and 10% for genetic and 179 morphological traits. We first prioritized areas to include 50% of the land containing threatened 13 180 and endemic species using a complementarity-based algorithm [18]. Next, we selected sites to 181 include 10% of the land containing each one of the genetic and morphological traits of the 182 common species. We used a target of 50% for threatened and endemic species because the 17% 183 target used in the main text may be too low in some conservation planning contexts; for example, 184 conservation plans for critically endangered species may attempt to conserve at least 50% of 185 extant habitat [19,20]. We used a 10% target for genetic and morphological traits because the 186 17% target may be too high for widespread components of biodiversity, and 10% has seen 187 widespread use in conservation planning exercises [11,21-23]. For example, Illoldi-Rangel et al. 188 [20] used a 50% target for endemic species and a 10% target for non-endemics. We then 189 calculated the percentage of threatened and endemic species that had 50% of their habitat 190 included in sites selected to include 10% of the occurrences of the genetic and morphological 191 traits of common species. Finally, we calculated the percentage of threatened and endemic 192 species that had 50% of their habitat included in sites selected at random. Results indicate that 193 genetic and morphological traits of common species are effective surrogates for threatened and 194 endemic species insofar as sites selected to include the former contain significantly more 195 threatened and endemic species than sites selected at random. For example, on the “genetic and 196 morphological traits” curve in panel (A), the point with the x-coordinate 5% and the y-coordinate 197 15% has the following interpretation. If land comprising 5% of the study region is selected to 198 include intraspecific variation, then such land includes 15% of the threatened and endemic 199 species. (B) Targets: 34% for threatened and endemic species and 10% for the genetic and 200 morphological traits of common species. The target of 34% was utilized for threatened and 201 endemic species because it is twice as large as the 17% target used in the main text. We selected 202 sites to include 10% of the genetic and morphological traits for the reasons listed above. The 14 203 “genetic and morphological traits” curve is similar to panel (A) but the y-coordinates of the 204 points are higher because the target for the threatened and endemic species is lower than in (A). 205 Since the target is lower, the target is satisfied for a higher percentage of the threatened and 206 endemic species than in (A). In both panels, the range of the x-axis is zero to ten because the 207 target for the genetic and morphological traits was 10%. Sites selected to include 10% of the 208 occurrences of the genetic and morphological traits comprise approximately 10% of the total 209 area of the study region. 210 211 Figure S5. Effectiveness of genetic and morphological surrogates for threatened and 212 endemic species. This figure is the same as figure three of the main text except that in the latter 213 the target was 17% for all surrogates whereas here the target is 10%. The black line with white 214 circles represents the percentage of threatened and endemic species that is found in areas 215 designed to include unique intraspecific morphologic and genetic traits of common species. The 216 solid black line shows the percentage of threatened and endemic species in random areas. The 217 black line with white squares depicts areas selected to include occurrences of birds and 218 amphibians. The gray line represents environmental surrogates. Since the black line with white 219 circles is to the left of the other lines, areas designed to include intraspecific variation of 220 common species protect the highest percentage of threatened and endemic species. 221 CBD=Convention on Biological Diversity. 15 222 Figure S1. 223 16 224 Figure S2. 225 17 226 Figure S3 227 228 18 229 Figure S4 230 19 231 Figure S5 232 233 20