1 Article title: Climate change mitigation policies reduce the rate and magnitude 2 of ecosystem impacts 3 Short running title: Climate change mitigation and global ecosystem impacts 4 Author names: Andrew J. Hartley12, Richard J. J. Gilham1, Carlo Buontempo1 and 5 Richard A. Betts12 6 Author research addresses: 7 1 Met Office Hadley Centre, FitzRoy Road, Exeter, EX1 3PB, UK 8 2 Department of Geography, University of Exeter, The Queen's Drive, Exeter, 9 Devon, EX4 4QJ, UK 10 Correspondence author address and e-mail: 11 Met Office Hadley Centre, FitzRoy Road, Exeter, EX1 3PB, UK 12 andrew.hartley@metoffice.gov.uk 13 Article type: Research Paper 14 1 1 ABSTRACT 2 Aim 3 To show the impacts of climate change mitigation on the rate and magnitude of 4 change in the climate that influences large-scale ecosystems. 5 Location 6 Results are calculated for all terrestrial land areas free of ice, and summarized 7 for 35 places of high conservation priority. We focus on 6 areas of high 8 conservation priority: Altai-Sayan Montane Forests, Orinoco River and Flooded 9 Forests, Chihuahuan Deserts, Congo Basin, Southwest Australia, and Coastal 10 West Africa. 11 Methods 12 We use a simple metric of change based on statistical distance within the 13 Holdridge Life Zone classification space (Hdistance) to quantify ecosystem- 14 relevant change in climate between a baseline average climate (1961-1990) and 15 each year in a 150 year time series (1950-2099). We apply this metric to a 58 16 member ensemble of GCM projections, for a business as usual scenario and an 17 aggressive climate change mitigation scenario. The rate and magnitude of change 18 in the Hdistance is calculated for each ensemble member. 19 Results 20 We find that more than 50% of high conservation priority areas show divergence 21 in the rate and magnitude of change in the Hdistance metric when comparing a 22 business as usual emissions scenario (A1B) with an aggressive carbon dioxide 23 mitigation scenario (RCP2.6). In other high priority areas we find that potentially 24 important thresholds are exceeded even with small changes in the Hdistance 25 under scenario A1B. 2 1 Main conclusions 2 We conclude that potentially dangerous impacts to high priority ecosystems can 3 be avoided in many parts of the world by a global policy of aggressive climate 4 change mitigation. Even though in some cases, the long term magnitude of 5 change threshold is exceeded under RCP2.6, this generally occurs later in the 6 century, allowing more time for ecosystems to adapt. 7 8 KEYWORDS 9 Climate change; mitigation; conservation planning; ecosystem impacts; potential 10 ecosystems; Holdridge Life Zones; Perturbed Parameter Ensemble; WWF 11 Priority Places; Biodiversity 12 13 3 1 INTRODUCTION 2 Conservation planners need to know what challenges lie ahead for global 3 ecosystems and biodiversity if different courses of action are taken by the 4 world’s governments in response to anthropogenic climate change. This presents 5 challenges to climate scientists to ensure that policy relevant climate modeling 6 experiments are conducted and communicated effectively to users in the 7 conservation community. Likewise, in order for conservation science to progress 8 from the bioclimatic envelope approach, new methods need to be developed to 9 incorporate higher temporal resolutions of climate data into models of species’ 10 population dynamics (Huntley et al., 2010; Keith et al., 2008; Anderson et al., 11 2009). 12 13 To date, the majority of biodiversity impacts studies have chosen to use 14 temporally aggregated and spatially disaggregated changes derived from General 15 Circulation Models (GCMs; e.g. Tabor & Williams, 2010) under a variety of future 16 socio-economic scenarios (N. Nakicenovic et al., 2000). In doing so, potentially 17 important information on inter-annual or intra-seasonal variability has been 18 disregarded in biodiversity projections. Additionally, the spatial disaggregation 19 of GCM data creates greater uncertainty in conservation policies at ecoregion 20 and local scales (Wiens & Bachelet, 2010). As models for predicting the impact 21 of climate change on global biodiversity begin to consider interactions 22 between population dynamics and species’ ranges (Anderson et al., 2009), 23 conservation scientists must develop more robust methods to integrate 24 projections from large ensembles of GCMs that have been designed to 25 address specific climate change policy questions. Huntley et al. (2010) 4 1 propose that the next generation of integrated model should include climatic 2 and habitat suitability, population dynamics and dispersal ability. They 3 present this in the context of the range of species responses to the magnitude 4 and rate of change. They also argue that there is a role to play for models of 5 intermediate 6 information on species’ population responses to change. complexity, especially given the shortage of suitable 7 8 In this paper we report the outcome of using a relatively simple metric for 9 ecosystem change with an ensemble of GCM projections to assess the possible 10 rate and magnitude of ecosystem change. We compare the results obtained from 11 using both a 'business as usual' and an aggressive mitigation future scenario 12 with the aim of demonstrating the possible effect of policy decisions on 13 ecosystems. In addition, we aim to show projected changes in the context of 14 thresholds in the rate and magnitude of change. This is investigated using a 15 large ensemble of GCMs to explore uncertainties due to the parameterization 16 of the Hadley Centre model HadCM3C. The rate and magnitude of ecosystem 17 change is quantified using a new measure, defined as the distance of change 18 within the Holdridge Life Zone conceptual space. 19 5 1 METHODS 2 A new measure of ecosystem change 3 The Holdridge Life Zone system (Holdridge, 1967) was one of the first 4 classifications to relate climatic variables to large-scale ecosystems. It has the 5 advantage of being relatively simple to implement whilst allowing the objective 6 relation of temperature and precipitation variables to either potential biomes, 7 altitudinal zones or potential vegetation types (the combination of which was 8 termed “Life Zones” by Holdridge). An important caveat in this approach is 9 acknowledged in the term 'potential'. Climate is only one of many factors that 10 contribute towards determining the existence of a particular vegetation type at a 11 given time and location. Other factors that may influence vegetation type, such as 12 CO2 effects, ozone, nutrient availability and soil condition are not accounted for 13 by the Holdridge system. Nevertheless, we argue that the general approach is 14 still relevant, as many existing studies use temperature and precipitation 15 variables to quantify the impacts of climate change on species or ecosystems 16 (Velarde et al., 2005; Lugo et al., 1999; Good et al., 2011). 17 18 Rather than classifying particular grid cells into discrete Life Zones, we use the 19 axes of Mean Annual Biotemperature and Annual Precipitation as a means of 20 defining a statistical space that is relevant to ecosystems (see Appendix S1 in 21 Supporting Information for calculations). Within this statistical space, we 22 calculate the distance of change between a baseline climate and a future climate 23 (see Appendix S2). Since these axes are not orthogonal, a trigonometric 24 transformation is used to obtain the distance of separation between the baseline 25 and a given point in time (see Appendix S3). 6 1 2 This distance metric (Hdistance) can be thought of as a vector of movement 3 between two points within the Holdridge diagram (see Appendix S2). It provides 4 an objective measure of change between two time periods that allows 5 comparison of changes between different ecosystems in different climatic zones. 6 The use of Hdistance provides a continuous metric for evaluating the GCM 7 output. This represents an advantage over measuring discrete transitions from 8 one vegetation class to another. This will help to compare the ecosystem impacts 9 in different parts of the world, for example, whether the projected large warming 10 of the Russian tundra is a more or less disruptive ecosystem perturbation than 11 the wetting of the eastern Sahara. 12 13 Climate change projections 14 In this study we apply the Hdistance measure to a large ensemble of climate 15 change projections based on the HadCM3C General Circulation Model (GCM; 16 Booth et al., 2012). This is an atmosphere-ocean-carbon cycle coupled 17 configuration of the original HadCM3 model (Gordon et al., 2000). It is 18 configured to include additionally the main elements of the carbon cycle, via 19 dynamic vegetation and ocean exchange, as well as an interactive sulfur cycle 20 scheme to account for emissions-based air pollution. The model includes flux 21 adjustments to account for biases in the model sea surface temperatures and 22 salinity compared to historical observations, as described in Collins et al. (2010). 23 24 In order to capture uncertainties related to configuration of the GCM, a 58 25 member perturbed parameter ensemble was created. Each member of this 7 1 ensemble was configured with a set of parameters designed to explore the range 2 of uncertainty in the atmosphere, ocean, land carbon cycle and sulfur cycle. A 3 framework for such an approach can be found in Murphy et al. (2007), and this 4 Earth System Ensemble (ESE) is described in full by Lambert et al. (2012). Each 5 ensemble member was run using historical climate forcing from 1950 to 2000, 6 and two different scenarios between 2000 and 2099 (discussed below). While 7 the ensemble has a large number of members, the experiment was not designed 8 to provide probabilities of particular outcomes. It should be interpreted as a 9 means of exploring the range of credible outcomes from a GCM by sampling from 10 a large range of uncertainty. 11 12 We assessed the impacts of a climate change mitigation strategy by using two 13 distinct future greenhouse gas emissions scenarios. Firstly, the IPCC Special 14 Report on Emissions Scenarios (SRES) A1B scenario (N. Nakicenovic et al., 2000) 15 was used to represent a ‘business as usual’ scenario in which the world 16 continues to be more integrated with a balanced emphasis on all energy sources. 17 Secondly, the Representative Concentration Pathway 2.6 (RCP 2.6, also referred 18 to as RCP 3PD) was used to simulate a scenario of aggressive greenhouse gas 19 mitigation policy (Moss et al., 2010; see Fig. 1). Each scenario was used to force 20 the 58 member ESE, with the resulting difference used to show the effect an 21 aggressive mitigation policy may have on global ecosystems. It should be noted 22 that while each ensemble member is forced by two different emissions scenarios, 23 the total radiative forcing depends on the perturbed parameters for the 24 interactive carbon and sulfur cycles in each ensemble member. Additionally, 25 since the emissions from RCP2.6 effectively remain constant from approximately 8 1 2020 and then reduce after 2050 (see Fig. 1), the ecosystem changes from 2 RCP2.6 show the changes that we have already committed to as a result of the 3 delayed response of the Earth system to historic greenhouse gas emissions. 4 5 6 Distance of change 7 For each ensemble member and emissions scenario, the Hdistance was 8 calculated (see Appendix S3). Mean annual biotemperature and mean annual 9 precipitation were calculated for a period of 1961 to 1990 (beginning in January 10 1961 ending in December 1990), and used to calculate the Hdistance between 11 this baseline period and each individual year in the 150 year time series (from 12 1950 to 2099). By calculating Hdistance over the historical period, we obtain a 13 measure of how much we would expect Hdistance to vary under normal climatic 14 conditions. If we make the reasonable assumption that ecosystems are in 15 equilibrium with the current climate, we may regard the Hdistance over the 16 observed period as an indication of the natural variability of this measure. In 17 other words, this is the degree to which we would expect the climate to vary 18 year-to-year without inducing an ecosystem change. 19 20 Rate and magnitude of change 21 We calculated the mean Hdistance for each decade in the 150 year time series, 22 relative to the 1961-1990 baseline, to give the decadal magnitude of change. The 23 rate of change is calculated for each year (t0) by subtracting the mean annual 24 Hdistance for the previous 10 years (t-11 to t0) from the mean annual Hdistance 25 for the next 10 years (t0 to t11). This annual rate of change was then averaged for 9 1 each decade to give the mean decadal rate of change in the Hdistance. The time 2 series of magnitude of change in the Hdistance is presented according to a 3 selection of WWF Priority Places. These are areas selected as a focus for 4 conservation activity by WWF, based on a combination of their diversity and 5 abundance of life, threats they face and WWF’s ability to make a positive impact 6 within the next decade (see Fig. 2). 7 10 1 RESULTS 2 3 We present here results for the following 6 WWF Priority Places: Altai-Sayan 4 Montane Forests, Orinoco River and Flooded Forests, Chihuahuan Deserts and 5 Freshwater, Congo Basin, Southwest Australia and West Africa Marine 6 (Terrestrial part). These regions (see Fig. 2) were selected as examples of the 7 variety of change in the rate and magnitude of Hdistance. A summary of the 8 changes found in all Priority Places can be found in Table 1. This summarises 9 whether or not divergence was found between the two scenarios, and whether 10 or not the A1B crossed a threshold of rate or magnitude. 11 12 We plotted the time series of change in the ensemble mean of Hdistance for each 13 Priority Place and both emissions scenarios (Fig. 3), with the shaded area 14 showing 1 standard deviation around the mean for each scenario. Additionally, 15 based on the information in Fig. 3, we plot for each decade, the mean rate of 16 change in the Hdistance against the total magnitude of change relative to the 17 1961-90 baseline (Fig. 4). Error bars show 1 standard deviation around the 18 decadal mean rate and magnitude of change in Hdistance. This figure also shows 19 the changes in relation to potentially important thresholds. These thresholds 20 represent the baseline variability in the Hdistance and can be interpreted as the 21 upper limits to variability in Hdistance between 1961-1990. The thresholds for 22 both magnitude and rate of change in Hdistance are based on all ensemble 23 members and scenarios for the 1961-1990 period compared to the 1961-1990 24 mean climate. For a given ensemble member and scenario, the Hdistance 25 between each year and the 1961-1990 mean climate was calculated, with the 11 1 threshold magnitude being the mean magnitude of change plus 1 standard 2 deviation. For rate of change, the upper threshold was set at 1 standard 3 deviation greater than the mean. 4 12 1 DISCUSSION 2 3 All WWF Priority Places show a steady increase in the Hdistance over time, 4 irrespective of greenhouse gas emissions scenario (Fig. 3). However, a clear 5 divergence emerges between the A1B scenario and RCP2.6 scenarios from 6 approximately 2050 in most Priority Places. Fig. 4 shows that this divergence is 7 more pronounced in the Altai-Sayan Montane Forests and Orinoco River Priority 8 Places (the full list of places where this occurs can be found in table 1). It is 9 notable that in the Altai-Sayan, the threshold for the rate of change is 10 considerably lower (0.025) than in the Orinoco River Priority Place (0.044). This 11 has a consequence of the mean rate of change exceeding the threshold between 12 the 1990s and 2030s in Altai-Sayan under RCP2.6. In contrast, the mean rate of 13 change under RCP 2.6 does not exceed the threshold in Orinoco River. It is also 14 notable that while the rate and magnitude thresholds are exceeded in the 15 ensemble mean for A1B, the uncertainty, shown by horizontal and vertical bars 16 around each decade, is much greater in Orinoco River Priority Place. 17 18 The Chihuahuan Desert, Congo Basin and Southwest Australia Priority Places are 19 examples of places where there is little or no divergence between A1B and 20 RCP2.6. While there is some divergence between the ensemble mean, the range 21 of uncertainty from the GCM ensemble overlaps considerably. However, these 22 locations also show the importance of the threshold value. For all 3 places, the 23 rate and magnitude thresholds are not exceeded under RCP2.6, because either 24 the inter-decadal change is minimal (Congo Basin), or because the thresholds are 25 relatively high (Chihuahuan Desert and Southwest Australia). In contrast, the 13 1 low threshold for the Congo Basin is exceeded under A1B, albeit due to a modest 2 increase in rate and magnitude. We also observe that despite high thresholds in 3 the terrestrial part of the West Africa Marine Priority Place, the magnitude of 4 change under A1B still exceeds the threshold of rate and magnitude. 5 6 A main advantage of this approach is the ability to compare changes across very 7 different ecosystems. We propose that the Hdistance is used as a measure for 8 setting global scale conservation priorities for adaptation to climate change. In 9 comparison to results from assessments of velocity of climate change 10 (Dobrowski et al., 2012; Loarie et al., 2009), the Hdistance is a continuous 11 measure of the magnitude and rate of change at a certain location. Also, in 12 contrast to the majority of biodiversity impacts assessments that rely on the 13 identification of suitable habitats (e.g. Thomas et al., 2004; G.F. Midgley et al., 14 2002), this approach is compatible with the coarser resolution of GCMs without 15 relying on uncertain downscaling techniques (Wiens & Bachelet, 2010; Trivedi et 16 al., 2008). Furthermore, in comparing A1B to RCP2.6, we provide conservation 17 planners and policy makers with information on the impacts of aggressive 18 climate change mitigation policies. Using the examples that we present, it is clear 19 that ecosystem impacts are not globally uniform, and in many cases can be 20 avoided if carbon dioxide emissions peak in approximately 2020 and decline 21 thereafter. 22 23 Despite these advantages, we acknowledge that the magnitude and rate of 24 change in the Hdistance is not influenced by the resilience of ecosystems, or the 25 ability of ecosystems to adapt to climate change in situ. Therefore, we 14 1 recommend that this information be used in conjunction with species or 2 ecosystem vulnerability assessments (such as Foden et al., 2008; Wilson et al., 3 2005; Summers et al., 2012). 4 15 1 CONCLUSIONS 2 We have presented a new annual measure of ecosystem change, Hdistance, that 3 can be used as a basis for comparing the impact of climate change on large scale 4 ecosystems across different conservation regions of the world. 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His current 4 research interests lie in the novel application of climate science to advise 5 conservation planners and further improvement of earth system models. 6 23 1 TABLES WITH THEIR CAPTIONS Scenario Divergence No Scenario Divergence Altai-Sayan (T) African Rift Lakes Amazon Guianas (T) Atlantic Forests Amur-Heilong (T) Borneo Chihuahuan Desert (T) Cerrado-Pantanal (T) Choco-Darien (T) Coastal East Africa Eastern Himalayas (T) Congo Basin (T) Fynbos (T) Cora Triangle Greater Black Sea Basin Miombo Woodlands (T) Lake Baikal New Guinea Mediterranean (T) Southwestern Australia (T) Mekong Complex (T) Sumatra Namib-Karoo (T) Western Ghats Northern Great Plains (T) Orinoco (T) South Chile (T) Yangtze 2 Table 1. WWF Priority Places in which divergence did or did not occur between 3 scenarios. Divergence indicates locations at which a climate change mitigation 4 scenario is projected to reduce the rate and magnitude of ecosystem change 5 relative to the A1B scenario. Locations marked with (T) indicate places where 6 the A1B scenario crosses either the rate or magnitude threshold by the 2090s. 7 24 1 FIGURE LEGENDS 2 Figure 1. Carbon dioxide emissions, expressed as gigatonnes of carbon per year, 3 for SRES scenario A1B and RCP2.6. 4 5 Figure 2. Location of all WWF Priority Places, and the subset selected for this 6 study shown in Mollweide equal area map projection. 7 8 Figure 3. Time series of change in the Hdistance relative to the 1961-1990 9 baeline period. The solid lines show the ensemble mean, and semi-transparent 10 zone shows 1 standard deviation around the ensemble mean. Values are 11 smoothed using a 10-year moving average. 12 13 Figure 4. Decadal changes in rate and magnitude of change in Hdistance under 14 RCP2.6 and A1B, relative to the 1961-1990 baseline period. Black doted lines 15 denote inter-annual variability (1 standard deviation) in the rate and magnitude 16 of change during the baseline period (1961-1990) for each Priority Place. 17 25 1 FIGURES -1 CO2 emissions æèGtC y öø 15 10 Scenario A1B RCP2.6 5 0 1850 4 1900 1950 2000 Year 2 3 Figure 1. 5 26 2050 2100 27 Southwest Pacific Choco-Darien Amazon Guianas Southern Chile Southern Ocean Southern Ocean Atlantic Forests Atlantic Forests Orinoco River and Flooded Forests Southeastern Rivers and Streams Fynbos Namib-KarooKaokoveld African Rift Lakes Region Miombo Woodlands Congo Basin West Africa Marine Mediterranean Coastal East Africa Southwest Australia Madagascar African Rift Lakes Region Sumatra Borneo Mekong Complex Yangtze Basin Amur-Heilong Western Ghats Eastern Himalayas Greater Black Sea Basin Lake Baikal New Guinea and Offshore Islands Southern Ocean Southwest Pacific Coral Triangle 2 Cerrado-Pantanal Galapagos Chihuahuan Deserts and Freshwater Northern Great Plains Altai-Sayan Montane Forests Arctic Seas and Associated Boreal/Tundra WWF Priority Places 1 Figure 2. Hdistance 28 0.0 0.2 0.4 0.6 0.8 1.0 0.0 0.2 0.4 0.6 0.8 1.0 0.0 0.2 0.4 0.6 0.8 1.0 1975 2000 2025 Southwest Australia 2050 2075 2100 Years 1975 2000 2025 West Africa Marine Congo Basin 2050 Orinoco River and Flooded Forests Hdistance for WWF Priority Places Chihuahuan Deserts and Freshwater Altai−Sayan Montane Forests 2075 2100 RCP2.6 A1B Scenario 1 Figure 3. WWF Priority Places Altai−Sayan Montane Forests 0.9 Orinoco River and Flooded Forests 0.8 0.7 0.6 ● ● 2080 2080 ● ● 2070 2070 ● 0.5 2060 ● ● 2060 2050 0.4 ● ● ● ● ● 2070 2050 2040 2080 2060 0.2 ●● ● ● ●● 2040 ● ● 1980 1980 1960 1960 11970 970 ● ● ● 0.1 2050 ● 2080 2060 ● ● 2050 2040● ● ● 2030 2030 ● 2020 ● 2020 ● 2010 ● ● ● 2010 ● ● ● ● ● 2000 ● ● 2000 1990 1980 1980 1990 1960 1960 1970 1970 2070 2030 2030 ● ● 2020 ● 2020 ● 2010 ● ● 2010 2000 2000 ● ● 1990 1990 0.3 ● 2040 0.0 Chihuahuan Deserts and Freshwater 0.9 Congo Basin 0.8 0.7 Magnitude 0.6 0.5 Scenario ● 2080 2070 ● 2060 ● 2050 ● a A1B ● 0.4 ● ●● ● ● ● ● a RCP2.6 ● 2040 2050 20602070 2080 ● ●2040 ● 2030 ●● 2030 2020 ●2020 2010 2010 ● ● 2000 ● ● ●● ●2000 ●1990 1990 19601980 1960 1970 1970 1980 0.3 0.2 ● 2080 ● ● ● 2070 2060 ● 20502040 ●●● ● ● ● 2080 2070 2060 2050●● ● 2030 2040 2030 ●2020 ●2020 ● 2010 ●●●● ●●2010 20002000 1990 1980 1960 1990 1980 1960 1970 1970 0.1 0.0 Southwest Australia 0.9 West Africa Marine 0.8 ● 2080 0.7 ● 2070 ● 0.6 2060 ● ● 0.5 2070 ● 2060 2050 ● 2080 ● ● 0.4 ● ● ● ● 2040 ●2070 ● 2080 2050 ● ● 2060 2030 2040 ● ●2030 2020 ● 2020 ● ● ● ●●2000 2010 ●● 2010 ● ●● 1990 2000 1990 1970 1960 1960 1980 1980 1970 0.3 ● ● ● ● 2050 2080 2050 2070 2060 2040 ● 2040● ● ● 2030 ● 2030 ● 2020 ● 2020 ●● ● ● 2010 2010 ● ● ●● 2000 2000 1990 ● 1990 1980 ● 1970 1980 1960 1960 1970 ● 0.2 0.1 0.0 −0.025 1 2 0.000 0.025 0.050 −0.025 0.075 Rate Figure 4. 3 29 0.000 0.025 0.050 0.075 1 SUPPORTING INFORMATION 2 Additional Supporting Information may be found in the online version of this 3 article: 4 5 Appendix S1 Equations for calculation of Holdridge input variables 6 Appendix S2 The Holdridge Life Zone system 7 Appendix S3 Calculation of the Hdistance 8 9 As a service to our authors and readers, this journal provides supporting 10 information supplied by the authors. Such materials are peer-reviewed and may 11 be reorganized for online delivery, but are not copy-edited or typeset. Technical 12 support issues arising from supporting information (other than missing files) 13 should be addressed to the authors. 14 30 1 Supplementary Material 2 Appendix S1: Equations for calculation of Holdridge input variables 3 Biotemperature is calculated as the sum of all mean monthly temperatures that 4 are above freezing, divided by 12. The equation is as follows: ti 30 Tbio t ti 0 i 12 5 6 where ti = mean monthly temperature in degrees Celsius for a given 30 year 7 period. 8 9 10 Annual precipitation is calculated as the sum of total monthly precipitation. The equation is as follows: i 12 Pann pi i 1 11 12 where pi = total monthly precipitation in mm per month, averaged over a given 13 30 year period. 14 31 1 Appendix S2: The Holdridge Life Zone system B F 2 3 The axes used for calculating the Hdistance are shown in red (note they are not 4 orthogonal). The example shows a change from a mean baseline climate (B) to a 5 future climate (F) due to an increase in annual precipitation and mean annual 6 biotemperature. Note the log scale of both mean annual biotemperature and 7 annual precipitation. Source: Holdridge (1967) 8 32 1 Appendix S3: Calculation of the Hdistance 2 The first step in our procedure was to identify a suitable metric for calculating 3 distances between points B and F shown in Appendix S2. Given that the axis of 4 the two state variables (biotemperature and annual precipitation) are not 5 perpendicular to one another it was necessary to define an additional variable in 6 order to correctly calculate the Euclidian distance between two points in 7 Holdridge space: 8 9 10 11 d= ( b2 - b1 ) + ( r'2 - r'1 ) 2 2 We used biotemperature (b) as a Y-axis and we designed the accessory variable r' to be orthogonal to the Y-axis. This was defined by the relationship: r' = r - btan(30°) 12 where 30° is the angle between the two axes in the original diagram and r is the 13 value of annual precipitation. Such a relationship can be obtain through 14 trigonometry, accounting for the fact that in the original Holdridge diagram, the 15 lines of constant annual precipitation do not cross the annual precipitation axis 16 at a 90° angle but rather at 120°. 17 The figure below shows the trigonometry used for calculating the distance (d) 18 between points B (baseline) and F (future). 33 r' K B Bio Temperature R' d r b F Annual Precipitation 1 2 The Holdridge space is defined by the biotemperature and annual precipitation 3 axes. Since these axes are not orthogonal to one another, they cannot be used to 4 calculate the Euclidian distances within the Holdridge space. An additional 5 variable was therefore defined to overcome this problem (R'), which can be 6 constructed using the two existing axes. A mathematical relationship linking the 7 two can be identified once we consider that: 8 9 1) B-r' =BK- r'K 10 2) BKr is an equilateral triangle (all angles being 60°) from which it follows that 11 BK=Br 12 3) r'K/sin (30) =b*sin(60) with 60° being the angle in K and 30° the angle in F of 13 the triangle r'FK 14 34 1 Considering also that both axes are linear in their log form, the Euclidian 2 distances (d) in this space becomes: 3 d= ( log(b2 ) / log(b1 )) + ( log(r2 ) / log(r1 ) - log(b2 ) / log(b1 )tan(30)) 2 4 35 2