Literature DB >> 34938503

Projected impacts of climate change on snow leopard habitat in Qinghai Province, China.

Jia Li1, Yadong Xue2,3, Charlotte E Hacker4, Yu Zhang5, Ye Li2,3, Wei Cong2,3, Lixiao Jin2,3, Gang Li6, Bo Wu1, Diqiang Li2,3, Yuguang Zhang2,3.   

Abstract

Assessing species' vulnerability to climate change is a prerequisite for developing effective strategies to reduce emerging climate-related threats. We used the maximum entropy algorithm (MaxEnt model) to assess potential changes in suitable snow leopard (Panthera uncia) habitat in Qinghai Province, China, under a mild climate change scenario. Our results showed that the area of suitable snow leopard habitat in Qinghai Province was 302,821 km2 under current conditions and 228,997 km2 under the 2050s climatic scenario, with a mean upward shift in elevation of 90 m. At present, nature reserves protect 38.78% of currently suitable habitat and will protect 42.56% of future suitable habitat. Current areas of climate refugia amounted to 212,341 km2 and are mainly distributed in the Sanjiangyuan region, Qilian mountains, and surrounding areas. Our results provide valuable information for formulating strategies to meet future conservation challenges brought on by climate stress. We suggest that conservation efforts in Qinghai Province should focus on protecting areas of climate refugia and on maintaining or building corridors when planning for future species management.
© 2021 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd.

Entities:  

Keywords:  National park; adaptive strategies; habitat corridors; suitable habitat; vulnerability

Year:  2021        PMID: 34938503      PMCID: PMC8668752          DOI: 10.1002/ece3.8358

Source DB:  PubMed          Journal:  Ecol Evol        ISSN: 2045-7758            Impact factor:   2.912


INTRODUCTION

Earth's climate is facing unprecedented changes (Garcia et al., 2014). Recent assessments by the Intergovernmental Panel on Climate Change (IPCC) have reported that the global average temperature has increased by 0.85 ᵒC over the last one hundred years and that warming trends will continue in the near future regardless of attempts to curtail greenhouse gas emissions (IPCC, 2014). This has emerged as a key threat for global biodiversity conservation (Arneth et al., 2020). Previous studies have shown the impacts of climate change on wildlife population dynamics (Martay et al., 2017; Tanentzap et al., 2020), distribution (Pastor, 2016; Sántiz et al., 2016), phenology (Koleček et al., 2020), evolution (Karell et al., 2011 ), and invasive species (Bertelsmeier et al., 2013). These impacts are expected to be exacerbated in future (Bellard et al., 2012). Natural selection provides a mechanism whereby species can adapt to changes in their environments (Rinawati et al., 2013). Species persistence depends on the ability to reduce or avert climate change challenges through dispersal to suitable climatic areas, or through ecological plasticity (e.g., morphological, physiological, or behavioral traits) and evolutionary responses to global changes (Bellard et al., 2012; Charmantier et al., 2008; Foden et al., 2016; Seebacher et al., 2015). However, because of existing stressors, many species have reduced capacity to cope and will be at an increased risk of extinction (Schloss et al., 2012). One synthesis estimated that one in six species are likely to be at increasingly high risk of extinction if a “business as usual” mentality surrounding carbon emissions continues (Urban, 2015). It is imperative to identify the species and habitats that are most vulnerable to climate change (Foden et al., 2013). This poses an immense challenge for conservation biologists. Accurately predicting the impacts of climate change is difficult (Foden et al., 2018). Assessments of species vulnerability based on species distribution models (SDMs, such as MaxEnt) can be valuable tools for management and conservation (Li et al., 2018; Rowland et al., 2011). These modeling approaches correlate current species range and variables retrieved from databases to forecast shifts in species’ distribution under future climate scenarios (Guisan et al., 2013; Zhang, Clauzel, et al., 2019). The vulnerability of a species can then be assessed by comparing the differences in currently suitable versus future suitable habitat areas (Arribas et al., 2012; Sudo et al., 2019). Forecasts of large habitat contractions, expansions, or minimal overlap between current and future ranges can be used as indexes of species vulnerability (Carvalho et al., 2010; Guisan & Thuiller, 2005). Several analyses have provided examples of species likely to be vulnerable to climate change. For example, Hatten et al. (2016) used SDMs to identify bird and reptile vulnerabilities in the southwestern United Sates and found that nearly two‐thirds of the species’ suitable habitat was predicted to contract. Li et al. (2017) used modeling to assess the vulnerability of giant pandas (Ailuropoda melanoleuca) to future climate change and subsequently identified potential refugia and habitat corridors to be used in future conservation action plans. The snow leopard (Panthera uncia) occupies high mountain regions in Central Asia. Their distribution covers an area of more than 1.2 million km2 across 12 countries (Snow Leopard Network, 2014). The wild population consists of approximately 4000–7000 individuals (Li et al., 2016; Snow Leopard Network, 2014), although there is substantial uncertainty (Ale & Mishra, 2018; Liu et al., 2019). The snow leopard was listed as Endangered on the IUCN red list from 1972 to 2017 and is currently listed as Vulnerable (McCarthy et al., 2017). The primary threats to snow leopard survival include prey depletion, poaching and retaliatory killing, and habitat loss and fragmented due to climate change and human settlement expansion (Aryal, 2017; Li et al., 2016; McCarthy et al., 2017; Valentová, 2017). Although conservation efforts have improved snow leopard populations in some areas (Liu et al., 2016; Xu et al., 2008), the metapopulation continues to show a decreasing trend in number of individuals. To date, studies of snow leopard ecology have included population genetics (Janecha et al., 2014; Karamachary et al., 2011; Zhang, Hacker, et al., 2019; Zhou et al., 2014), habitat selection (Weiskopf et al., 2016; Xu et al., 2006), foraging strategy (Anwar et al., 2011; Hacker et al., 2021; Suryawanshi et al., 2017), activity (McCarthy et al., 2005; Tang et al., 2017), and home range (Johansson et al., 2016). In recent years, the snow leopard has attracted public attention and studies on its conservation have diversified, now including climate change (Forrest et al., 2012; Li et al., 2016), human‐snow leopard conflict (Hacker et al., 2020; Li et al., 2013; Sullivan et al., 2018), illegal trade (Ma, 2012; Maheshwari & Niraj, 2018), and conservation landscapes (Li et al., 2020). However, data remain limited in comparison to other charismatic species (Suryawanshi et al., 2019). China holds over half of currently known suitable snow leopard habitat and plays a vital role in maintaining the entirety of the snow leopard population (McCarthy & Chapron, 2003). The snow leopard population size and distribution suffered extensively due to poaching and illegal trade from the 1950s to 1980s in China (Li et al., 2013; Valentová, 2017). Over the past few decades, the Chinese government has implemented conservation action plans to protect wildlife, including snow leopards. This has involved the strengthening of laws against poaching and trade, the establishment of nature reserves and pastureland rehabilitation (Li & Lü, 2014; Li et al., 2013). At present, most pre‐existing key threats and limiting factors for species across China are being mitigated. For snow leopards, populations are even recovering in some areas (e.g., the Sanjiangyuan region; Liu et al., 2016). However, most areas in snow leopard habitat (e.g., the Qinghai‐Tibetan Plateau) are ecosystems vulnerable to climate change (Peng et al., 2012; Yuke, 2019), and the World Wildlife Fund for Nature (WWF) has stated that more than a third of current snow leopard habitat may be lost due to increasing global warming (Sharma et al., 2015). Previous work surrounding climate change impacts on the snow leopard have been done in China. Li et al. (2016) found that 26% of currently suitable habitat in China would be lost under a mild climate scenario. However, the occurrence data used in the study only went to the year 2008, and thus, more recent assessments are needed. Forrest et al. (2012) investigated climate change in the Himalayas and found that 25% of snow leopard habitat in southern China would be lost under a high emissions scenario. While this area is one of the most important areas in China for snow leopard distribution, it represents only a small portion of known habitat. Other areas of China, such as Qinghai Province, also require fine scale investigation in regard to climate change. Qinghai Province holds some of the largest suitable stretches of continuous snow leopard habitat and is a very important distribution area in China (Liu et al., 2016). In this province, a total of 28 nature reserves have been established to protect snow leopards and other sympatric species (Zheng, 2011). In addition, the Sanjiangyuan and Qilian mountain reserves were upgraded as pilot national parks in 2017, integrating current nature reserves to resolve the problems of fragmented distribution and management. Given this area's importance to the species in China, it is critical to assess the vulnerability of the snow leopard to future climate change in Qinghai Province and to adopt adaptive conservation strategies to reduce its adverse impacts. Here, we built a snow leopard distribution model based on current species occurrence data and associated bioclimatic and environmental variables. We aimed to (a) identify currently suitable snow leopard habitat and distribution areas, and assess the vulnerability of snow leopard habitat in Qinghai Province to climate change from the current period to the 2050s; (b) identify climate refugia that could support the population during periods of climatic stress; (c) establish habitat corridors that could facilitate individual movement among patches of suitable habitat; and (d) determine how protected areas will be impacted by climate change, and provide conservation strategies under the future climate change scenario.

METHODS

Study area

Qinghai Province is located in the northeastern corner of the Qinghai–Tibetan Plateau in China (Figure 1). It covers an area of 720,000 km2, with a population of 5 million people (Zheng, 2011). Qinghai Province holds the source of the Yellow River and Yangtze River, as well as the upper reach of the Lancang (Mekong) River. The area consists primarily of grasslands, rangelands, deserts, and wetlands, with most mountains having an average altitude of above 4000 m. The climate is a typical plateau continental climate, dry and cold and with long winters, short summers, frequent winds, little rainfall, long hours of sunshine, and stark differences in temperature between day and night. The average annual temperature is −4°C (ranging from −20°C in January to 8°C in July), the average annual rainfall is 150–420 mm, and a clear warming trend with increased precipitation has occurred over the past several decades (Peng et al., 2012). The primary mammal species in addition to the snow leopard in Qinghai Province include the Eurasian lynx (Lynx lynx), Tibetan brown bear (Ursus arctos), desert cat (Felis bieti), wild yak (Bos mutus), Tibetan antelope (Pantholops hodgsonii), blue sheep (Pseudois nayaur), alpine musk deer (Moschus chrysogaster sifanicus), and the Eurasian otter (Lutra lutra; Zheng, 2011).
FIGURE 1

Mapping of the study area in China, thinned localities of snow leopard, nature reserves, and national parks in Qinghai Province. Codes of the reserves: 1‐Qilian Mountain; 2‐Datongbeichuanheyuan; 3‐Qinghai lake; 4‐Mengda; 5‐Keluke lake; 6‐Suosuolin; 7‐Nuomuhong; 8‐Huyang forest; 9‐Sanjiangyuan‐Maixiu; 10‐Sanjiangyuan‐Zhongtie Jungong; 11‐Sanjiangyuan‐Animaqin; 12‐Sanjiangyuan‐Xingxing lake; 13‐Sanjiangyuan‐Zalinghu Elinghu lake; 14‐Sanjiangyuan‐Yueguzonglie; 15‐Sanjiangyuan‐Nianbao Yuze; 16‐Sanjiangyuan‐Make river; 17‐Sanjiangyuan‐Duoke river; 18‐Sanjiangyuan‐Tongtian river; 19‐Sanjiangyuan‐Dongzhong; 20‐Sanjiangyuan‐Jiangxi; 21‐Sanjiangyuan‐Baiza; 22‐Sanjiangyuan‐Ansai; 23‐Sanjiangyuan‐Guozong Muzha; 24‐Sanjiangyuan‐Dangqu; 25‐Sanjiangyuan‐Suogartoma river; 26‐Sanjiangyuan‐Gela Dangdong; 27‐Hoh Xil; 28‐Longbao

Mapping of the study area in China, thinned localities of snow leopard, nature reserves, and national parks in Qinghai Province. Codes of the reserves: 1‐Qilian Mountain; 2‐Datongbeichuanheyuan; 3‐Qinghai lake; 4‐Mengda; 5‐Keluke lake; 6‐Suosuolin; 7‐Nuomuhong; 8‐Huyang forest; 9‐Sanjiangyuan‐Maixiu; 10‐Sanjiangyuan‐Zhongtie Jungong; 11‐Sanjiangyuan‐Animaqin; 12‐Sanjiangyuan‐Xingxing lake; 13‐Sanjiangyuan‐Zalinghu Elinghu lake; 14‐Sanjiangyuan‐Yueguzonglie; 15‐Sanjiangyuan‐Nianbao Yuze; 16‐Sanjiangyuan‐Make river; 17‐Sanjiangyuan‐Duoke river; 18‐Sanjiangyuan‐Tongtian river; 19‐Sanjiangyuan‐Dongzhong; 20‐Sanjiangyuan‐Jiangxi; 21‐Sanjiangyuan‐Baiza; 22‐Sanjiangyuan‐Ansai; 23‐Sanjiangyuan‐Guozong Muzha; 24‐Sanjiangyuan‐Dangqu; 25‐Sanjiangyuan‐Suogartoma river; 26‐Sanjiangyuan‐Gela Dangdong; 27‐Hoh Xil; 28‐Longbao

Species records

A total of 1291 snow leopard occurrence records in Qinghai Province were obtained from camera‐trap monitoring, signs (including footprints, scrapes), genetically verified scat samples, and published literature from 2005 to 2020 (see details in Appendix S1; Figure 1). Because these occurrence records are from multiple unplanned surveys, the records likely display spatial autocorrelation (Kramer‐Schadt et al., 2013). To correct for this, we thinned occurrence records using a thinning distance of 10 km (Radosavljevic & Anderson, 2013). To correct for the effect of sample selection bias on predictive performance (Vanderwal et al., 2009), we randomly generated 10,000 pseudo‐absence points with the exclusion of a 40 km (the maximum daily movement distance of a snow leopard; McCarthy et al., 2005) buffer area from snow leopard occurrence records in the study area to consider dispersal ability in both suitable habitat and gap analyses.

Environmental variables

Nineteen bioclimatic variables for current (average for 1950–2000) and future (average for 2041–2060, henceforth referred to as the 2050s) climate conditions were downloaded from the WorldClim database (available at http://www.worldclim.org) at 30‐second resolution. The future projection was extracted from HadGEM2‐AO general circulation models of the IPCC‐CMIP5 under the representative concentration pathway (RCP4.5; Beak et al., 2013). RCP4.5 represents a mild climate change scenario with increases in the average global temperature of 0.9–2.0°C for the 2050s, which would fall within a 2°C global warming limit (UNFCCC, 2015). The time horizon of the 2050s was selected as this period is far enough into the future for marked changes to have occurred (Young et al., 2012). Additional environmental variables at the same resolution were used to construct snow leopard distribution models. The density of settlements, roads, railways, and rivers were obtained from the Resource and Environment Science and Data Center of China website (http://www.resdc.cn/Default.aspx). Elevation was obtained from a digital elevation model with 30‐second resolution from the WorldClim database, and slope data derived from elevation (see details in Appendix 1). Nonclimatic variables were unavailable for the 2050s, and thus, we kept these variables static in our projections (Li et al., 2017; Stanton et al., 2012). All variables were resampled at a 1‐km2 resolution and put into the same projection using ArcGIS 10.4 (ESRI Inc.). SDMtoolbox (Brown, 2014) was used to determine multicollinearity of variables. One variable of each relational pair was removed where Pearson's correlation coefficients of |r| > .6 (Appendix 2; Cord et al., 2014). The most biologically meaningful variables to the snow leopard were retained (Bai et al., 2018; Li et al., 2016).

Habitat suitability model

Maximum Entropy Models (MaxEnt software version 3.3.3k) are considered a useful and superior tool to build habitat suitability models with presence‐only data (Elith et al., 2011). With this model, performance is measured under the receiver operating characteristic curve (AUC) with a value closer to 1 representing a near perfect model. Snow leopard occurrence data were divided into random training tests (AUCtest: 75%) and testing tests (AUCtrain: 25%). We ran 10 replicates and conducted a subsample procedure with recommended default settings. Variable importance was estimated by the permutation importance method (Wisz et al., 2008). The predicted area under the curve (AUC) was used as the performance estimator of the model. The logistic results of the MaxEnt model were considered to represent the probabilities of species occurrence (Phillips et al., 2006). We then binarized potential presence/absence areas according to the maximum training sensitivity average plus the specificity logistic threshold (Li et al., 2018; Songer et al., 2012). Areas with probability values above the threshold were regarded as suitable snow leopard habitat. Based on criteria of prioritized protecting habitat set by Global Snow Leopard and Ecosystem Protection Program (Snow Leopard working Li et al., 2020; Secretariat, 2013), we defined continuous area larger than 10,000 km2 as core suitable habitat (calculated in ArcGIS 10.4).

Gap analysis of protected areas

Networks of protected areas remain the most valuable resource for snow leopard persistence. We overlapped current and future suitable habitats with the borders of established nature reserve and national parks to explore the conservation effectiveness of these reserves in protecting snow leopards under the future climate change scenario using ArcGIS 10.4.

Vulnerability assessment

We assessed changes in suitable habitat between the current time frame and the 2050s and categorized resulting habitat as follows: (i) Unsuitable habitat: area where habitat that was not suitable for snow leopards in current and future climate projections; (ii) Vulnerable habitat: area in which currently suitable habitat was projected to be unsuitable in the 2050s; (iii) Climate refugia: area where currently suitable habitat overlapped with predicted suitable habitat for the 2050s; (iv) Newly suitable habitat: area where currently unsuitable habitat was predicted to become suitable by the 2050s. Three indicators were used to assess habitat vulnerability: (i) percentage of suitable habitat area change (AC); (ii) percentage of currently suitable habitat area lost by the 2050s (SHL); and percentage of increased suitable habitat area for the 2050s (SHI). Indicators were calculated as follows: For the formulas above, SHf is the area of predicted suitable habitat for snow leopard under the 2050s climatic scenario; SHc is the area of currently suitable habitat; and SHo is the area of overlapped suitable habitat between present time and the 2050s (Li et al., 2018; Thuiller et al., 2005). We used a Mann–Whitney U test to compare the change in average suitable habitat elevation between the current time frame and the 2050s. Data were expressed as mean ± standard error (Mean ± SE). Statistical significance was considered at p < .05. Statistical analyses were performed in SPSS 19.0 (IBM Inc.).

Habitat connectivity analysis

Linkage Mapper identifies wildlife corridors and suitable habitat patches via connectivity analyses (McRae & Kavanagh, 2011). The inverse of the logistic output from the resulting MaxEnt model was used as a measure of movement resistance for the snow leopard and least‐cost linkages were mapped between core habitat areas (>500 km2 based on the mean home range of snow leopard; Johansson et al., 2020). The least‐cost pathways (LCP) and corridors were implemented in the Linkage Mapper toolbox (ArcGIS 10.0‐10.6; https://circuitscape.org/linkagemapper/).

RESULTS

Species distribution model

A total of 400 occurrence records and eight variables were used in the final MaxEnt model as model parameters. The habitat suitability model provided satisfactory results with an average training AUC value of 0.906 (±0.004) and average testing AUC of 0.895 (±0.016). The percent contribution of each model variable ranked from highest to lowest was as follows: annual mean temperature (23.8%), density of rivers (22.3%), temperature constancy (16.9%), precipitation of driest month (12.7%), mean diurnal range (12.7%), density of settlements (10.5%), slope (2.9%), and density of railways (1.5%). The average threshold value for the measure of suitable habitat was 0.336.

Changes in habitat suitability

Under current conditions, the area of suitable snow leopard habitat in Qinghai Province was 302,821 km2 (Table 1; Figure 2), predominately distributed in 31 counties (area of suitable habitat larger than 1000 km2). In Tianjun, Qilian, Xinghai, Dulan, Zadoi, Chindu, Zhiduo, Qumarleb, Maqin, Maduo, Yushu, Zhiduo, and Golmud, the area of suitable habitat was larger than 10,000 km2 and appears to be distributed in continuous patches. By the 2050s, the area of suitable habitat decreased by 24.38% (Area Change, AC) to 228,997 km2. Suitable habitat areas larger than 1000 km2 dropped from 31 to 22 counties, and only 9 had more than 10,000 km2 (Tianjun, Qilian, Dulan, Zadoi, Zhiduo, Qumarleb, Maduo, Golmud, and Dari).
TABLE 1

Predictions of the suitable habitat area (km2) for snow leopard in Qinghai Province in the current period and the 2050s

City or prefectureCountySuitable habitat areaPercentage of area change (AC)
Current2050s
Xining cityDatong1916.171392.50−27.33%
Huanzhong110.15107.80−2.14%
Huanyuan337.97601.4177.95%
Haidong cityLedo665.49433.60−34.84%
Minhe92.5117.78−80.78%
Huzhu1916.241703.03−11.13%
Hulong273.4097.82−64.22%
Xunhua165.6219.65−88.14%
Haibei Tibetan Autonomous PrefectureMenyuan5532.315532.310.00%
Qilian10,351.1010,347.40−0.04%
Haiyan2362.681831.53−22.48%
Gangca9345.956039.00−35.38%
Hainan Tibetan Autonomous PrefectureTongren1838.93211.31−88.51%
Jianza374.510.00−100.00%
Zeku1867.85368.66−80.26%
Henan1740.5734.36−98.03%
Gonghe3835.112233.76−41.75%
Tongde2124.52631.43−70.28%
Guide1218.24405.06−66.75%
Xinghai10,507.468425.29−19.82%
Guinan4839.81308.27−93.63%
Guoluo Tibetan Autonomous PrefectureMaqin12,059.518319.80−31.01%
Baima1279.680.00−100.00%
Gade5318.43464.17−91.27%
Dari6382.371111.95−82.58%
Jigzhi3374.80153.14−95.46%
Maduo23,856.6519,789.76−17.05%
Yushu Tibetan Autonomous PrefectureYushu12,165.758154.52−32.97%
Zadoi25,520.8620,953.95−17.89%
Chindu12,501.975147.07−58.83%
Zhiduo29,266.0428,247.93−3.48%
Nangqian4360.341859.18−57.36%
Qumarleb35,788.1535,553.55−0.66%
Haixi Mongolian and Tibetan Autonomous PrefectureHaixi3562.893651.172.48%
Golmud15,126.8016,463.618.84%
Delingha7136.885544.70−22.31%
Wulan606.62278.79−54.04%
Dulan25,546.3120,204.27−20.91%
Tianjun17,551.1612,358.01−29.59%

Under the current conditions, area of suitable habitat for snow leopard in Qinghai Province was 302,821 km2, and dramatically reduced to 228,997 km2 by the 2050s due to climate change, representing a decreased of 24.38%.

FIGURE 2

Suitable snow leopard habitat distributed in the nature reserves and national parks of Qinghai Province. (a) Suitable habitat under the current climate scenario; (b) predicted habitat suitability by the 2050s under a future mild climate change scenario

Predictions of the suitable habitat area (km2) for snow leopard in Qinghai Province in the current period and the 2050s Under the current conditions, area of suitable habitat for snow leopard in Qinghai Province was 302,821 km2, and dramatically reduced to 228,997 km2 by the 2050s due to climate change, representing a decreased of 24.38%. Suitable snow leopard habitat distributed in the nature reserves and national parks of Qinghai Province. (a) Suitable habitat under the current climate scenario; (b) predicted habitat suitability by the 2050s under a future mild climate change scenario Climate change would also result in an upward shift of suitable habitat (Figure 3). The average elevation of suitable habitat in the 2050s was projected to be 4395 ± 478 m, which is significantly higher (z = −17.91, p < .001) than that of current suitable habitat (4306 ± 503 m).
FIGURE 3

Impacts of climate change on the potential distribution of snow leopard in Qinghai Province for elevation. The y‐axis represents the percentage of grid cells with a 500 m elevation interval

Impacts of climate change on the potential distribution of snow leopard in Qinghai Province for elevation. The y‐axis represents the percentage of grid cells with a 500 m elevation interval

Coverage of protected areas

Results showed that current nature reserves protected 38.78% of currently suitable habitat and 42.56% suitable habitat in the 2050s (Table 2; Figure 2). By the 2050s, 23 nature reserves will have a decrease in suitable snow leopard habitat, among which Maixiu (AC = −77.97%), Zhongtie Jungong (AC = 43.22%), Nianbao Yuze (AC = 94.68%), Tongtian river (AC = −44.09%), Dongzhong (AC = −15.63%), Jiangxi (AC = 50.35%), Baiza (AC = −53.62%), Dangqu (AC = −61.78%), Suogartoma river (AC = −7.58%), and Gela Dangdong (AC = −23.94%) nature reserves are estimated to suffer most extensively. Climate change will only scarcely increase the distribution of snow leopards in some nature reserves, mainly in Hoh Xil (AC = 29.06%), Ansai (AC = 19.78%), and Yueguzonglie (AC = 3.97%).
TABLE 2

The predicted changes in suitable habitat for snow leopard in nature reserves and national parks

Nature reserveSuitable habitat areaPercentage of area change (AC)
Current2050s
1‐Qilian mountain4857.624834.75−0.47%
2‐Datongbeichuanheyuan1082.03816.73−24.52%
3‐Qinghai lake289.360.00−100.00%
4‐Mengda0.000.00
5‐Keluke lake0.000.00
6‐Suosuolin47.510.00−100.00%
7‐Nuomuhong0.000.00
8‐Huyang forest0.000.00
9‐Sanjiangyuan‐Maixiu1478.10325.63−77.97%
10‐Sanjiangyuan‐Zhongtie Jungong6954.343948.92−43.22%
11‐Sanjiangyuan‐Animaqin4265.194127.19−3.24%
12‐Sanjiangyuan‐Xingxing lake6782.516777.70−0.07%
13‐Sanjiangyuan‐Zalinghu Elinghu lake13,525.7712,545.41−7.25%
14‐Sanjiangyuan‐Yueguzonglie3894.504049.183.97%
15‐Sanjiangyuan‐Nianbao Yuze1757.5993.54−94.68%
16‐Sanjiangyuan‐Make river80.060.00−100.00%
17‐Sanjiangyuan‐Duoke river85.820.00−100.00%
18‐Sanjiangyuan‐Tongtian river8172.064568.65−44.09%
19‐Sanjiangyuan‐Dongzhong2672.432254.70−15.63%
20‐Sanjiangyuan‐Jiangxi1103.84548.01−50.35%
21‐Sanjiangyuan‐Baiza2853.421323.32−53.62%
22‐Sanjiangyuan‐Ansai1228.431471.4719.78%
23‐Sanjiangyuan‐Guozong Muzha10,020.999593.62−4.26%
24‐Sanjiangyuan‐Dangqu7809.322984.43−61.78%
25‐Sanjiangyuan‐Suogartoma river32,328.4829,879.40−7.58%
26‐Sanjiangyuan‐Gela Dangdong1027.30781.31−23.94%
27‐Hoh Xil5050.836518.5029.06%
28‐Longbao82.2827.54−66.53%
Sanjiangyuan National Park66,294.7861,259.74−7.59%
Qilian Mountain National Park9518.849513.21−0.06%

Current nature reserves protected 38.78% of currently suitable habitat and 42.56% of suitable habitat in the 2050s.

The predicted changes in suitable habitat for snow leopard in nature reserves and national parks Current nature reserves protected 38.78% of currently suitable habitat and 42.56% of suitable habitat in the 2050s. With regard to national parks, Sanjiangyuan and Qilian Mountain protected 25% of currently suitable habitat area and 30.9% of suitable habitat area in the 2050s (Table 2; Figure 2). Sanjiangyuan national park will lose 7.59% (AC) of its suitable habitat by the 2050s, but suitable habitat in Qilian Mountain will remain stable and is an area of climate refugia. Our model predicted that 90,480 km2 (SHL = 30%) of currently suitable habitat for the snow leopard is vulnerable to climate change (Figure 4). Unchanged suitable habitat (i.e., climate refugia) covers an area of 212,341 km2 and is mainly distributed in the counties of Qumarleb, Maduo, Zadoi, Yushu, Xinhai, Dulan, and Golmud in Sanjiangyuan, and Menyuan, Gangca, and Tianjun in Qilian Mountain. Our results also showed an increase in suitable habitat (16,656 km2; SHI = 7.27%) scattered throughout Zhiduo, Golmud, and Gonghe.
FIGURE 4

Vulnerability levels of suitable habitat for snow leopard. A total 30% of currently suitable habitat for snow leopard would be vulnerable to climate change in Qinghai Province

Vulnerability levels of suitable habitat for snow leopard. A total 30% of currently suitable habitat for snow leopard would be vulnerable to climate change in Qinghai Province

Gap analysis

Gap analysis showed areas of suitable habitat at the junction of Qumarlep and Chindu and surrounding areas (G1; Figure 5), and at the junction of Qilian, Gangca and Tianjun (G2; Figure 5). These areas are largely unprotected, leaving significant gaps in the current conservation network. Reserves should be established in these locations to provide suitable habitat patches that are stable and can contribute to the improvement of habitat connectivity.
FIGURE 5

Protection gaps within the current conservation network for suitable snow leopard habitat in Qinghai Province. G1–G2 indicates protection gaps

Protection gaps within the current conservation network for suitable snow leopard habitat in Qinghai Province. G1–G2 indicates protection gaps

Potential habitat corridors

Suitable habitat patches for the snow leopard connected by least‐cost pathways (LCP) represent potential corridors between core habitat areas (>500 km2). Linkage Mapper mapped 20 least‐cost potential corridors between currently suitable habitat patches (Table 3; Figure 6), with the average LCP being 68 km (ranging from 4 to 322 km). Linkage Mapper mapped 13 least‐cost potential corridors in the 2050s, with the average LCP being 127 km (ranging from 5 to 444 km).
TABLE 3

Characteristic of linkages between snow leopard suitable habitat patches in Qinghai Province in the current period and the 2050s

Currently suitable habitat patches2050s suitable habitat patches
HC IDFrom SHPTo SHPLCP (km)HC IDFrom SHPTo SHPLCP (km)
L11218L11644
L21852L236326
L3349L346126
L43863L4415196
L54674L5610444
L64744L679149
L74824L791523
L858322L8101186
L96721L9101487
L106882L10111275
L117853L1112139
L1281272L12121578
L13814148L1313145
L1491197
L1591439
L16101334
L17101462
L1811137
L1912144
L201314134

Abbreviations: HC, Habitat corridor; LCP, Least cost patch length; SHP, Suitable habitat patch.

FIGURE 6

The potential corridors between current and future core suitable habitat patches for snow leopard in Qinghai Province

Characteristic of linkages between snow leopard suitable habitat patches in Qinghai Province in the current period and the 2050s Abbreviations: HC, Habitat corridor; LCP, Least cost patch length; SHP, Suitable habitat patch. The potential corridors between current and future core suitable habitat patches for snow leopard in Qinghai Province The establishment of potential corridors will be a long‐term process and does not address the more urgent needs for species conservation. Rather, habitat corridors should be based on increasing the likelihood for known isolated populations to shift into core suitable habitat patches (L14–L18 and L3–L7; Figure 6) and assisting genetic exchange between the Sanjiangyuan and Qilian Mountain populations (L12–L13; Figure 6).

DISCUSSION

Species listed as Threatened or Endangered are at risk of extinction due to the adverse effects of natural and anthropogenic stressors. Climate change, either by acting alone or by exacerbating the effects of current stressors, constitutes an important new threat for many of these species (Arribas et al., 2012). Based on our results, even under a mild climate change scenario, about 25% of currently suitable snow leopard habitat in Qinghai Province is projected to be lost. Research on how snow leopards may respond to these changes will allow researchers to circumvent the challenges associated with anticipated climate changes and to tailor conservation strategies with potential species distribution shifts in mind. Historically, snow leopards were found in all the major mountain ranges of Qinghai Province as well as in various small massifs (Schaller et al., 1988). However, due to a variety of threats to species persistence, the snow leopard's population and distribution rapidly decreased, with evidence of some local extirpation events (Li & Lü, 2014). Fortunately, the fate of snow leopards improved once they were listed as a Class I State Key Protected Wild Animal in 1989 in China (Li et al., 2016). The Chinese government has implemented conservation programs to protect and improve habitat for wildlife including the snow leopard, which serves as a recognizable flagship species for conservation. This has been very successful in some areas (Liu et al., 2016). China has recently launched an ambitious program to establish a national park system that integrates current protected areas to resolve problems associated with fragmented management (Xu et al., 2019). As the first location of the system's ten national parks, Qinghai Province has provides approximately 200,000 km2 of strictly protected area (Sanjiangyuan and Qilian Mountain), offering a new way for comprehensive, complete and continuous protection of at‐risk species. But whether or not this habitat can be sustained within the context of climate change remains uncertain. Therefore, the assessment of habitat vulnerability is a valuable tool to prioritize conservation strategies that reduce the impact of climate change on species such as the snow leopard. Core distribution areas are important because they serve as connective hubs, allowing for greater genetic exchange between populations (Duan et al., 2016). Our results showed that climate change would not only shrink currently suitable snow leopard habitat along the edges of Qinghai Province, but also within their core distribution areas (e.g., Xinghai, Yushu, Maqin, and Chindu), making them more fragmented. For example, currently suitable habitat along the eastern and southern edges of Qinghai Province (e.g., Hennan and Jigzhi, which currently have a relatively small population of snow leopards based on camera‐trap data; Forestry and Environmental Protection Bureau of Hennan county, 2018; Xiao et al., 2019) were relatively isolated and fragmented, and were projected to experience the greatest degree of habitat loss. Snow leopards in these regions will be limited by natural and artificial barriers if they attempt to disperse toward core distribution areas during periods of climatic stress. Therefore, effective conservation strategies for these regions should consider the maintenance of current corridors and the potential construction of additional migration corridors to facilitate dispersal to larger core areas. The Qinghai–Tibetan Plateau is the world's highest, largest, and youngest plateau (Erkan et al., 2011). The warming rate of the Tibetan Plateau is more than twice the Northern Hemisphere average and is predicted to continue or accelerate in this century (Peng et al., 2012; Yuke, 2019). Our results predicted that the area of suitable snow leopard habitat will decrease in future, and that mean elevations of suitable habitat will shift to higher altitudes, similar to previous findings from past studies (Li et al., 2016). The snow leopard inhabits alpine and subalpine zones that lie between the snow and tree line (Snow Leopard Network, 2014). With the temperature warming, these zones will move up toward mountaintops, resulting in an overall decrease of snow leopard habitat and increase of habitat fragmentation (Forrest et al., 2012). To make matters worse, an upward shift in the tree line will inevitably cause changes in vegetation communities, which will cause shifts in where snow leopard prey species, such as the blue sheep, forage. These areas may be closer to pastoralist communities, making snow leopards more likely to encounter and kill livestock (Aryal et al., 2013, 2014). Protected areas provide the most effective approach for biodiversity conservation, yet they are failing to protect species from future climate change (Hannah et al., 2007). Most protected areas were established decades ago. Their locations were typically based on empirical information and expert opinion (Xu et al., 2014), without consideration for climate change (Araùjo et al., 2011). Range shifts due to climate change may cause species to move out of protected areas, thereby resulting in reducing the relevance of current fixed protected areas in future conservation strategies (Monzón et al., 2011). Our results revealed that loss of suitable snow leopard habitat would affect the conservation effectiveness of current nature reserves in Qinghai Province. These nature reserves do not adequately protect currently suitable habitat for the snow leopard (Figure 6), and they are poorly suited for accommodating species range shifts. The further construction of national parks provides an opportunity to design them while considering the impacts of climate change, such as climate induced range shifts, in China. Assessments of vulnerability can provide valuable information about the locations that are vulnerable to climate change, enabling managers to make appropriate conservation and management strategies in light of expected future climate warming (Pacifici et al., 2015). Based on our results, conservation actions must be focused on those regions, which are predicted to suffer from large range contractions. These regions present the greatest risk to future snow leopard persistence. Vulnerability assessments also identify potential climate refugia for snow leopard within the Qinghai Province. These areas of relatively unchanged suitable habitat may facilitate species persistence during periods of climatic stress and thus warrant protection. As a flagship species in China, snow leopards are a heavy focus for conservation efforts. The government of China has listed snow leopards in the key program of biodiversity conservation and has established two national parks (Sanjiangyuan and Qilian Mountains) specifically for protecting species in Qinghai Province (Ministry of Environmental Protection, 2011). Although the last two decades have seen remarkable advancements in our knowledge of snow leopard status and ecology, numerous gaps in knowledge remain. Sustainable conservation strategies require comprehensive information on the status and ecology of the snow leopard. The species’ response to climate change and which management strategies will be most be effective will require long‐term standardized monitoring programs. Non‐climate‐related stressors, such as domestic livestock, feral dogs, and disease, also challenge snow leopard conservation (Li et al., 2019). Domestic animals are a potential prey item for snow leopards, and they opportunistically kill livestock even if wild prey are available and abundant (Suryawanshi et al., 2017). In addition, Tibetan mastiff ownership is loose and the population is growing (Liu, 2018). Camera traps in the Qilian Mountains frequently detected Tibetan mastiffs in snow leopard distribution areas (Xue et al., 2019), indicating that predation pressure and competition could become a growing problem. Furthermore, snow leopards can harbor viruses that may negatively impact their health if the animal is experiencing environmental stress (Johansson et al., 2020). These stressors may produce synergic effects that would increase the adverse impacts of climate change on the species. Thus, mitigating these would help to minimize the net negative impact of climate change. Validation of our results revealed that there was good concordance between known distribution of the snow leopard in Qinghai Province and the suitable habitat predicted by the model. Nevertheless, our study had some limitations. First, snow leopard habitat is impacted by other physical and biological factors. However, data on biotic and abiotic factors in Qinghai Province are rare, which restricted our choice variables for building the model. Second, our findings ignore the interactions of ecological processes on the snow leopard in response to climate change. Regardless, our results represent a reliable analysis of the impacts of climate change on snow leopard distribution and are based on the best data available for the species in Qinghai Province.

CONCLUSION

We assessed the impact of climate change on suitable snow leopard habitat, evaluated conservation effectiveness of existing nature reserves, and identified areas of climate refugia and habitat corridors in Qinghai Province, China. Under a mild climate change scenario, our results revealed that the overall area of suitable habitat was predicted to decrease in future, and that mean elevations of suitable habitat will shift upward. We suggest that future nature reserves be in areas that are currently unprotected but have climate refugia, that current migration corridors be maintained, that long‐term monitoring efforts increase, and that actions aimed at mitigating non‐climate‐related stressors continue. Our results provide valuable information for formulating strategies to mitigate the future challenges brought on by climate stress in Qinghai Province, an area which is vital to the persistence of the snow leopard in China.

CONFLICT OF INTEREST

None declared.

AUTHOR CONTRIBUTIONS

Jia Li: Conceptualization (equal); Data curation (equal); Formal analysis (equal); Investigation (equal); Methodology (equal); Resources (equal); Software (equal); Supervision (equal); Validation (equal); Writing‐original draft (equal); Writing‐review & editing (equal). Yadong Xue: Data curation (equal); Formal analysis (equal); Investigation (equal); Software (equal); Writing‐original draft (equal). Charlotte E. Hacker: Writing‐review & editing (equal). Yu Zhang: Data curation (equal); Investigation (equal). Ye Li: Investigation (equal). Wei Cong: Formal analysis (equal). Lixiao Jin: Formal analysis (equal); Investigation (equal). Gang Li: Investigation (equal). Bo Wu: Investigation (equal). Diqiang Li: Formal analysis (equal); Funding acquisition (equal); Investigation (equal); Software (equal); Validation (equal); Writing‐review & editing (equal). Yuguang Zhang: Data curation (equal); Funding acquisition (equal); Investigation (equal); Methodology (equal); Writing‐original draft (equal); Writing‐review & editing (equal). Appendix S1 Click here for additional data file.
VariableDescriptionUnitTypeMinMaxMeanSD
Bio1Annual mean temperature°CContinuous−131129.00−11.0442.05
Bio2Mean diurnal range°CContinuous102172.00143.849.34
Bio3Temperature constancyContinuous3047.0037.283.11
Bio4Temperature seasonalityContinuous587012,104.008390.321157.66
Bio5Max temperature of warmest month°CContinuous40360.00165.3353.36
Bio6Min temperature of coldest month°CContinuous−320−25.00−217.3734.81
Bio7Annual temperature range°CContinuous284500.00382.7034.35
Bio8Mean temperature of wettest quarter°CContinuous−28265.0091.0846.85
Bio9Mean temperature of driest quarter°CContinuous−224116.00−110.2639.46
Bio10Mean temperature of warmest quarter°CContinuous−28266.0092.1548.37
Bio11Mean temperature of coldest quarter°CContinuous−23743.00−122.6437.24
Bio12Annual precipitationmmContinuous171177.00327.26205.11
Bio13Precipitation of wettest monthmmContinuous6231.0075.7740.38
Bio14Precipitation of driest monthmmContinuous09.001.661.34
Bio15Precipitation seasonalityContinuous74151.00101.1611.38
Bio16Precipitation of wettest quartermmContinuous13645.00201.00113.00
Bio17Precipitation of driest quartermmContinuous035.006.795.06
Bio18Precipitation of warmest quartermmContinuous13645.00200.50112.77
Bio19Precipitation of coldest quartermmContinuous035.007.325.10
SlopeSlope°Continuous071.7517.7913.39
SetdesDensity of settlementm/km2 Continuous02039.6069.66150.50
RoddesDensity of roadm/km2 Continuous0103.837.678.83
RivdesDensity of riverm/km2 Continuous025.683.903.43
RaidesDensity of Railwaym/km2 Continuous013.750.571.54
EleElevationmContinuous7956191.003903.61977.34
LayerBio1Bio2Bio3Bio4Bio5Bio6Bio7Bio8Bio9Bio10Bio11Bio12Bio13Bio14Bio15Bio16Bio17Bio18Bio19SlopeSetdesRoddesRivdesRaidesEle
Bio11.00
Bio2.431.00
Bio3−.16.301.00
Bio4.36.24−.831.00
Bio5.94.48−.40.661.00
Bio6.93.27.07.06.771.00
Bio7.51.47−.69.96.77.191.00
Bio8.95.44−.38.62.99.81.731.00
Bio9.91.49.11.13.79.92.30.801.00
Bio10.96.44−.39.621.00.81.731.00.811.00
Bio11.93.37.18−.01.74.98.16.78.92.781.00
Bio12−.06−.26.65−.86−.39.17−.78−.33.07−.33.261.00
Bio13−.18−.33.66−.89−.50.07−.84−.44−.05−.44.15.981.00
Bio14−.01−.27.48−.69−.28.19−.63−.22.10−.23.26.83.791.00
Bio15−.41.16.00.19−.22−.44.10−.27−.30−.27−.49−.51−.40−.611.00
Bio16−.15−.31.66−.89−.47.10−.83−.41−.01−.41.18.991.00.81−.431.00
Bio17.01−.24.52−.73−.28.21−.65−.23.11−.23.29.91.85.96−.65.881.00
Bio18−.16−.31.66−.89−.48.09−.83−.42−.02−.42.17.991.00.81−.431.00.881.00
Bio19−.03−.26.52−.73−.31.16−.65−.26.07−.26.24.89.84.96−.63.86.99.861.00
Slope−.09−.24.09−.23−.16.00−.25−.15−.03−.15−.01.25.23.21−.15.25.23.25.221.00
Setdes.31−.10.03−.14.18.37−.09.21.28.22.38.27.24.17−.33.24.21.23.18.131.00
Roddes.40−.12−.05−.09.26.44−.04.30.32.31.45.28.24.21−.42.24.24.24.21.12.821.00
Rivdes.00−.13.36−.48−.19.12−.42−.16.05−.16.18.56.55.50−.38.56.52.56.50.16.33.401.00
Raides.28−.06−.30.26.31.23.24.32.16.32.20−.18−.19−.15−.15−.19−.16−.20−.18−.05.41.50−.011.00
Ele−.89−.32.52−.67−.95−.71−.76−.95−.71−.96−.68.33.45.27.32.42.24.43.28.09−.25−.34.16−0.341.00
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