Heterogeneous distributional responses to climate warming: evidence from rodents along a subtropical elevational gradient
- Zhixin Wen†1,
- Yi Wu†2,
- Deyan Ge1,
- Jilong Cheng1, 3,
- Yongbin Chang1, 3,
- Zhisong Yang4,
- Lin Xia1 and
- Qisen Yang1Email author
© The Author(s) 2017
Received: 15 November 2016
Accepted: 11 April 2017
Published: 20 April 2017
Understanding whether species’ elevational range is shifting in response to directional changes in climate and whether there is a predictable pattern in that response is one of the major challenges in ecology. However, so far very little is known about the distributional responses of subtropical species to climate change, especially for small mammals. In this study, we examined the elevational range shifts at three range points (upper and lower range limits and abundance-weighted range centre) of rodents over a 30-year period (1986 to 2014–2015), in a subtropical forest of Southwest China. We also examined the influences of four ecological traits (body mass, habitat breadth, diet and daily activity pattern) on the upslope shifts in species’ abundance-weighted range centres.
Despite the warming trend between 1986 and 2015, the 11 rodent species in analysis displayed heterogeneous dynamics at each of the three range points. Species which have larger body sizes and narrower habitat breadths, show both diurnal and nocturnal activities and more specialized dietary requirements, are more likely to exhibit upslope shifts in abundance-weighted range centres.
Species’ distributional responses can be heterogeneous even though there are directional changes in climate. Our study indicates that climate-induced alleviation of competition and lag in response may potentially drive species’ range shift, which may not conform to the expectation from climate change. Difference in traits can lead to different range dynamics. Our study also illustrates the merit of multi-faceted assessment in studying elevational range shifts.
KeywordsClimate change Heterogeneity Range shift Rodent Species traits Subtropical
The past 30 years have seen an accelerating increase in the global average surface temperature, and the warming trend is still continuing . One of the most striking biological impacts of ongoing climate warming is the upslope range shifts of organisms, especially when the vegetation and food resources they rely on occur successively at higher elevations [2–4]. There is a high risk of extinction for the species which are unable to keep pace with the climate change or cross the range-shift gaps , thus invoking a keen interest of ecologists and conservationists in elevational range shifts over recent decades.
Mountains are perhaps the best systems to investigate the interplay between climate change and species’ ranges because researchers can benefit from studying shifts in both range limits (i.e. upper and lower) of a species over relatively short spatial distances. For this reason, a substantial number of empirical studies (usually carried out at one or several mountain ranges) and meta-analyses [6, 7] have been conducted to explore species’ elevational range shifts, with the focal species including almost all the biotic groups on earth. Obviously, these studies have shown great variability in the observed responses. Notwithstanding a significant increase in temperature, species may show static distributions due to lag effect [8, 9], low mobility , acclimate to unfavorable climates  and behavioral thermoregulation instead of range shift ; and even counterintuitive downslope range shifts which are frequently explained by alleviation of species competition , water availability change , habitat modification [15, 16] and decreased precipitation . Moreover, it is indicated that species’ range dynamics are trait-dependent. Taking small mammals as an example, some life-history and ecological traits such as longevity , habitat preference  and diet  have been shown to affect the responses. Considering the complexity of potential mechanisms underlying elevational range shifts, it remains a great challenge to predict the shifting direction of species. The ability to make an accurate prediction will be valuable to the evaluation of future species assemblage structures at different elevations of a mountain.
Small mammals are sensitive to environmental change . To our knowledge, assessments of small mammal elevational range shifts by systematically resurveying historical sites were only seen in four elevational gradients of North America. Researchers found that small mammals showed much greater heterogeneity in range dynamics than that expected from warming [19, 21, 22]. In contrast to many other taxa, there has been little attention paid to small mammals in tropical and subtropical mountains, despite the fact that biotas here are more threatened by climate due to their generally narrower thermal niches [7, 23, 24]. Certainly, evidence from tropical and subtropical mountains is indispensable to gain an insightful understanding of the elevational range shifts of small mammals worldwide and compare the shifting directions and rates among different regions.
In this study, by revisiting historical sampling sites, we examined spatial shifts in rodent elevational ranges between historical (1986) and modern (2014–2015) times in a subtropical forest of Southwest China. Following Lenoir and Svenning , species’ range shift was simultaneously assessed at the upper range limit, lower range limit and range centre as their responses to climate change may differ [25, 26]. In addition, we related four species traits (body mass, habitat breadth, diet and daily activity pattern) to the upslope shifts in species’ abundance-weighted range centres. Our aims were to test (1) if species’ range shifts follow the same pattern as predicted from local climate change; and (2) if the selected traits could explain the difference in distributional responses among species.
Study area and climate data
The study area was an extensive elevational gradient (1550–3500 m) in the Wolong Nature Reserve (102°52′–103°24′E, 30°45′–31°25′N), Sichuan Province. Five vegetation types dominate at different elevations: evergreen broad-leaf forest (<1600 m); evergreen and deciduous mixed broad-leaf forest (1600–2100 m); coniferous and broad-leaf mixed forest (2100–2600 m); coniferous forest (2600–3100 m) and subalpine shrub and meadow (3100–3500 m). Most areas of this gradient have been fully protected since the early 1980s. Because of the extremely limited meteorological records (Dengsheng ecological station at 2800 m a.s.l., climate record available only from 1999 to 2008) in this reserve, we used climate data from the Dujiangyan meteorological station (698 m, approximately 68 km east of our study sites) to estimate the mean annual temperature (MAT) and total annual precipitation (TAP) trends between 1986 and 2015. During this period, MAT increased from 14.2 to 16.4 °C while TAP fluctuated greatly (Additional file 1: Fig. S1). Although the climate data came from a station outside our study area and were measured at a lower elevation than the sampling sites, they were the best available data in this region by far. It is also noted that MAT of Dengsheng ecological station increased by 0.6 °C between 1999 and 2008, with TAP showing little difference over time.
Historical and modern surveys
Detail information of sampling sites and sampling summary in 1986 and 2014–2015
All individuals (species)
Eleven species individuals (species)
Evaluating range shifts
We examined the shifts in upper range limit, lower range limit and abundance-weighted range centre of the 11 most common species (species with at least five captures in both periods, which formed the historical and modern datasets for comparison) between 1986 and 2014–2015. The abundance-weighted range centre of each period was calculated as:
To standardize the sampling effort, we randomly resampled (100 times without replacement) the historical and modern datasets to generate the identical number of individuals between periods at each site (e.g. 147 from the 186 individuals of 2014–2015 at site one, 72 from the 133 individuals of 1986 at site three; Table 1) , in the R environment (version 3.2.2). For each of the three range points, the average values derived from the 100 random resamplings of two periods were compared (modern value minus historical value) to evaluate the range shift.
To test whether an observed range shift at a given range point (range limits or centre) for a given rodent species was due to chance alone or it was a significant shift, we performed the species-level tests of significance regarding the magnitude of the observed range shift. Based on the 100 replicates of the initial datasets of two surveys, we first calculated the 100 paired differences (modern survey minus historical survey) for each of the three range points and for each of the 11 species, which produced a total of 3300 (100 × 3 × 11) elevational range shift values. For individual species, we then used three boxplots to illustrate its range shift results at different range points separately (one figure for the lower range limit, one for the lower range limit and one for the abundance-weighted range centre). Finally, each of the three boxplot was displayed against the zero reference line (i.e. no change over time) and a Student’s t test was conducted to determine whether the altitude of the focal point varied significantly between 1986 and 2014–2015.
Species traits in explaining upslope shifts in range centres
We used linear regression models to examine the effect of four species traits on the upslope shifts (downslope shifts were denoted by negative values) in species’ abundance-weighted range centres, which were body mass (average mass of adults captured in 1986 and 2014–2015), habitat breadth (number of habitat types for a species; obtained from IUCN ), diet (categorical variable: zero for herbivores or carnivores and one for omnivores; obtained from the MammalDIET dataset by Kissling et al. ) and daily activity pattern [zero for obligately diurnal or nocturnal (be active only in the daytime or only at night) rodents and one for facultatively diurnal (be active mostly at night but occasionally in the daytime) rodents]. The data of species traits are provided in Additional file 1: Table S1. These traits are associated with the climate-induced range shifts for a wide range of animals, including butterflies , birds [33, 34] and mammals [4, 18]. Some additional traits such as litters per year, longevity and adult mobility were not tested here because data were unavailable to include these traits which were investigated in other studies . Including these four traits as independent variables resulted in 15 possible models (Additional file 1: Table S2), and the best subset of models were selected by comparing their Akaike’s information criterion corrected for small sample size (AICC) . Because top-ranking models received nearly equivalent support (i.e., little difference in AICC values), we performed model averaging of coefficients on the models with ΔAICC ≤2 from the best model. This approach enabled us to assess the relative importance of each variable in predicting the upslope shift in range centre, according to their model-averaged standardized coefficients . Model selection and model averaging were performed using the R package “MuMIn” .
Species’ range shifts
Species traits in explaining upslope shifts in range centres
Model selection and model averaging results of models relating the upslope shifts (m) of 11 rodent species’ abundance-weighted range centres to four species traits (body mass, habitat breadth, diet and daily activity pattern), in the Wolong Nature Reserve between 1986 and 2014–2015
Model selection results
Model-averaged standardized coefficients (95% CI)
Parameter in model
−0.328 to 1.072
−1.03 to 0.402
−0.432 to 1.012
−0.903 to 0.586
Heterogeneous range shifts and potential causes
There has been a growing concern about the capacity of montane biotas to track the displacement of their climatic optima, but the evidence from subtropical zones is rare . Here, by comparing rodent elevational distributions across a 30-year interval, we demonstrate that despite a warming trend in a subtropical forest of China, there is heterogeneity in species’ distributional responses. Diverse patterns of range shift were revealed, including stasis, upslope and downslope range shifts. Many previous studies which reported species moving towards higher elevations in response to climate warming have also detected a portion of the investigated taxa showed no changes or downslope movements. In a global meta-analysis, Parmesan and Yohe  found that approximately 20% of the plant and animal species displayed downslope and southward range shifts. For plants, Lenoir et al.  demonstrated that in Northeast France, 53 of 171 (31%) species shifted their optimum elevations downslope between 1905–1985 and 1986–2005; and Wolf et al.  recently reported that merely 15% of the Californian plants’ mean elevations were higher than a century ago, and those of the rest species showed little or downslope movements. For birds, Tingley et al.  found that only half of the species in Sierra Nevada showed upslope shifts in upper or lower range boundary after a century of warming, possibly due to a relatively narrow elevational range over which bird eggs will hatch. As for small mammals which is our focal taxa, idiosyncratic patterns of elevational range shift have been borne out by several studies in North America [19, 21]. The disagreement between the observed range dynamics of rodents in Wolong and climatic expectations can be driven by a number of factors that shall be discussed below.
The upslope expansions of N. andersoni, E. melanogaster and R. norvegicus, and upslope contractions of C. eva and M. oeconomus, was probably a direct reaction to the increased temperature. As a non-native species, R. norvegicus may benefit from climate change in colonizing new habitats. When the temperature increases, non-native species usually tend to shift their ranges upslope to occupy the expanded potential niche space at higher elevations . Temporal changes in competitive species interaction may also result in the upslope shifts. In 1986, the upper limits of N. andersoni, E. melanogaster and R. norvegicus were situated at 1550 m where the rodents had the highest species richness (eight species) along the gradient, implying an intense interspecific competition at this elevation with the competitors most likely to consist of ecologically similar species (e.g. three Niviventer species ; also see Additional file 1: Table S1). The competition can be provisionally alleviated by climate warming, enabling species to fill their potential distribution areas by conducting an upslope (or downslope) range shift . By examining the dynamic of abundance-weighted range centre, it is possible to gain a more subtle insight into species’ distributional response. Although the change in range centre is closely linked with the change in range limits, upslope displacement of centre may manifest even though both boundaries remain unchanged, as found in Apodemus chevrieri. We would expect an imminent upslope range shift of the species provided the warming trend continues.
In our study, stasis was the most common dynamic (six of 11) at both range limits. By comparison, Moritz et al.  found that 36% of the small mammals in Yosemite National Park of California shifted their lower limits upslope. The different results between this and their research may be due to the different sampling intervals, which was a century in Moritz et al. . In Wolong, the increased temperature between 1986 and 2015 may be within the tolerance ranges of some thermotolerant species. Alternatively, less vagile species may need more than 30 years to display an evident upslope shift in lower limit (i.e. lag effect [9, 25]). The stasis of the upper limits of two species, A. latronum and M. oeconomus, deserve particular attention because they were historically located at the mountaintop. The impossibility to move “higher” may have strongly affected their range dynamics and made them more vulnerable to local extinction . Another interpretation of the static distributions is that species can use behavioral thermoregulation to prevent overheating, such as altering daily activity (e.g. reduce diurnal activity ) and hiding under vegetation shade . Besides, if there are desirable habitats around at the same elevation, rodents may prefer to migrate to these nearby refugia rather than conduct an arduous shift , as the North American elk (Cervus elaphus) did in an Idaho desert . Indeed, there are many cool environments in Wolong such as caves and shady valleys. These sites could facilitate the local persistence of species so that they can avoid long-distance vertical migration.
In line with many previous studies, we also observed downslope range shifts. The downslope expansion of A. latronum could be explained by the climate-induced alleviation of species competition , as long as predicable food and suitable habitats are available downwards. For Micromys minute, alleviated competition may be the same factor causing its downslope contraction, while changes in non-temperature factors like water availability could also underlie the movement . Our result was consistent with that reported in the Great Basin, where the downslope shifts of rodents were attributed to climate-induced floristic change and land use .
Range shifts related to species traits
The importance of species’ ecological traits in estimating and explaining climate-induced range shifts has been long recognized . We observed a positive, albeit not statistically significant, relationship between the body mass of rodents and upslope shift in species’ abundance-weighted range centre. This finding supports the idea that compared to smaller species, larger mammal species are generally more mobile [4, 45] and characterized by better abilities to colonize a new region on the basis of higher fecundities and larger home-range sizes . Intriguingly, differing from some earlier studies [18, 46, 47], habitat and dietary specialists were found showing greater upslope displacements at the range centres than generalists. We attribute our result to the strong dependence of specialists on specific prey and habitat. For example, the upslope shift in range centre of M. oeconomus (herbivore) could be driven by the upslope shift of its favored habitat (e.g. forest-meadow ecotone ) and plants. The phenomenon that habitat and dietary specialists shift upslope/northward more than generalists has also been observed in North American  and Central European  birds.
Our study represents one of the first attempts to explore the climate-induced elevational range shifts of subtropical small mammals. Using a multi-faceted assessment of range shifts (upper and lower range limits, abundance-weighted range centre) for 11 rodent species, we demonstrate that the distributional responses are heterogeneous despite a general warming trend, with stasis, upslope and downslope movements all being detected. The heterogeneity is possibly due to the difference in species traits such as body mass and habitat breadth. Climate-induced alleviation of competition and lag in response may potentially drive species’ range shift, which may not conform to the expectation from climate change.
- AICC :
Akaike’s information criterion corrected for small sample size
Institution of Zoology, Chinese Academy of Sciences
mean annual temperature
total annual precipitation
ZXW, YW and QSY conceived the idea and designed the research. DYG, JLC, YBC and ZSY conducted the field sampling. ZXW and LX analyzed the data, and ZXW and YW wrote the manuscript. All authors read and approved the final manuscript.
We are grateful to Wolong Nature Reserve Authority for permission to conduct the study. We thank Xiaogang Shi, Huanhuan Zhang, Yu Yang, Li Zhang, Lei Song and Yunfei Mu for their kind assistance in the field work.
The authors declare that they have no competing interests.
Availability of data and materials
Ethics approval and consent to participate
Our study was carried out in strict accordance with the animal research protocol IOZ-2006 approved by the Animal Care Committee of Institute of Zoology, Chinese Academy of Sciences (CAS).
Our study was supported by the National Science Fund for Fostering Talents in Basic Research (Special Subjects in Animal Taxonomy, NSFC-J1210002) and the Fund for Exploring the Biodiversity and Natural Resources of Wolong Nature Reserve (Y590911135).
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- IPCC. Climate Change 2013: the physical science basis. In: Working group I contribution to the fifth assessment report of the Intergovernmental Panel on Climate Change. New York: Cambridge University Press; 2013.
- Lenoir J, Svenning J-C. Climate-related range shifts—a global multidimensional synthesis and new research directions. Ecography. 2015;38:15–28.View ArticleGoogle Scholar
- Parmesan C. Ecological and evolutionary responses to recent climate change. Annu Rev Ecol Evol Syst. 2006;37:637–69.View ArticleGoogle Scholar
- Santos MJ, Thorne JH, Moritz C. Synchronicity in elevation range shifts among small mammals and vegetation over the last century is stronger for omnivores. Ecography. 2015;38:556–68.View ArticleGoogle Scholar
- Colwell RK, Brehm G, Cardelús CL, Gilman AC, Longino JT. Global warming, elevational range shifts, and lowland biotic attrition in the wet tropics. Science. 2008;322:258–61.View ArticlePubMedGoogle Scholar
- Chen I-C, Hill JK, Ohlemüller R, Roy DB, Thomas CD. Rapid range shifts of species associated with high levels of climate warming. Science. 2011;333:1024–6.View ArticlePubMedGoogle Scholar
- Gibson-Reinemer DK, Sheldon KS, Rahel FJ. Climate change creates rapid species turnover in montane communities. Ecol Evol. 2015;5:2340–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Popy S, Bordignon L, Prodon R. A weak upward elevational shift in the distributions of breeding birds in the Italian Alps. J Biogeogr. 2009;37:57–67.View ArticleGoogle Scholar
- Renwick KM, Rocca ME. Temporal context affects the observed rate of climate-driven range shifts in tree species. Glob Ecol Biogeogr. 2015;24:44–51.View ArticleGoogle Scholar
- Davis AJ, Jenkinson LS, Lawton JH, Shorrocks B, Wood S. Making mistakes when predicting shifts in species range in response to global warming. Nature. 1998;391:783–6.View ArticlePubMedGoogle Scholar
- Thuiller W, Lavorel S, Araújo MB. Niche properties and geographical extent as predictors of species sensitivity to climate change. Glob Ecol Biogeogr. 2005;14:347–57.View ArticleGoogle Scholar
- Kearney M, Shine R, Porter WP. The potential for behavioral thermoregulation to buffer “cold-blooded” animals against climate warming. Proc Natl Acad Sci USA. 2009;106:3835–40.View ArticlePubMedPubMed CentralGoogle Scholar
- Lenoir J, Gégout J-C, Guisan A, Vittoz P, Wohlgemuth T, Zimmermnn NE, Dullinger S, Pauli H, Willner W, Svenning J-C. Going against the flow: potential mechanisms for unexpected downslope range shifts in a warming climate. Ecography. 2010;33:295–303.Google Scholar
- Crimmins SM, Dobrowski SZ, Greenberg JA, Abatzoglou JT, Mynsberge AR. Changes in climatic water balance drive downhill shifts in plant species’ optimum elevations. Science. 2011;331:324–7.View ArticlePubMedGoogle Scholar
- Archaux F. Breeding upwards when climate is becoming warmer: no bird response in the French Alps. Ibis. 2004;146:138–44.View ArticleGoogle Scholar
- Cannone N, Sgorbati S, Guglielmin M. Unexpected impacts of climate change on alpine vegetation. Front Ecol Environ. 2007;5:360–4.View ArticleGoogle Scholar
- Tingley MW, Koo MS, Moritz C, Rush AC, Beissinger SR. The push and pull of climate change causes heterogeneous shifts in avian elevational ranges. Glob Change Biol. 2012;18:3279–90.View ArticleGoogle Scholar
- Angert AL, Crozier LG, Rissler LJ, Gilman SE, Tewksbury JJ, Chunco AJ. Do species’ traits predict recent shifts at expanding range edges? Ecol Lett. 2011;14:677–89.View ArticlePubMedGoogle Scholar
- Rowe RJ, Finarelli JA, Rickart EA. Range dynamics of small mammals along an elevational gradient over an 80-year interval. Glob Change Biol. 2010;16:2930–43.Google Scholar
- Pűettker T, Pardini R, Meyer-Lucht Y, Sommer S. Responses of five small mammal species to micro-scale variations in vegetation structure in secondary Atlantic Forest remnants, Brazil. BMC Ecol. 2008;8:9.View ArticleGoogle Scholar
- Rowe KC, Rowe KMC, Tingly MW, Koo MS, Patten JL, Conroy CJ, Perrine JD, Beissinger SR, Moritz C. Spatially heterogeneous impact of climate change on small mammals of montane California. Proc R Soc B. 2015;282:20141857.View ArticlePubMedPubMed CentralGoogle Scholar
- Moritz C, Patton JL, Conroy CJ, Parra JL, White GC, Beissinger SR. Impact of a century of climate change on small-mammal communities in Yosemite National Park, USA. Science. 2008;322:261–4.View ArticlePubMedGoogle Scholar
- Freeman BG, Freeman AMC. Rapid upslope shifts in New Guinean birds illustrate strong distributional responses of tropical montane species to global warming. Proc Natl Acad Sci USA. 2014;111:4490–4.View ArticlePubMedPubMed CentralGoogle Scholar
- Janzen DH. Why mountain passes are higher in the tropics. Am Nat. 1967;101:233–49.View ArticleGoogle Scholar
- Chen I-C, Hill JK, Shiu H-J, Holloway JD, Benedick S, Chey VK, Barlow HS, Thomas CD. Asymmetric boundary shifts of tropical montane Lepidoptera over four decades of climate warming. Glob Ecol Biogeogr. 2011;20:34–45.View ArticleGoogle Scholar
- Maggini R, Lehmann A, Kéry M, Schmid H, Beniston M, Jenni L, Zbinden N. Are Swiss birds tracking climate change? Detecting elevational shifts using response curve shapes. Ecol Model. 2011;222:21–32.View ArticleGoogle Scholar
- Wu Y, Hu J-C, Li H-C, Qu M-C. Research on community structure of small rodents in Wolong Nature Reserve. J China West Norm Univ. 1988;9:95–102.Google Scholar
- Wilson DE, Reeder DM. Mammal species of the world: a taxonomic and geographic reference. vol 2. 3rd ed. Baltimore: Johns Hopkins University Press; 2005.
- Menéndez R, Gonzélez-Megías A, Jay-Robert P, Marquéz-Ferrando R. Climate change and elevational range shifts: evidence from dung beetles in two European mountain ranges. Glob Ecol Biogeogr. 2014;23:646–57.View ArticleGoogle Scholar
- IUCN. http://www.iucnredlist.org/. Accessed Feb 2016.
- Kissling WD, Dalby L, Fløjgaard C, Lenoir J, Sandel B, Sandom C, Trøjelsgaard K, Svenning J-C. Establishing macroecological trait datasets: digitalization, extrapolation, and validation of diet preferences in terrestrial mammals worldwide. Ecol Evol. 2014;4:2913–30.View ArticlePubMedPubMed CentralGoogle Scholar
- Pöyry J, Luoto M, Heikkinen RK, Kuussaari M, Saarinen K. Species traits explain recent range shifts of Finnish butterflies. Glob Change Biol. 2009;15:732–43.View ArticleGoogle Scholar
- Auer SK, King DI. Ecological and life-history traits explain recent boundary shifts in elevation and latitude of western North American songbirds. Glob Ecol Biogeogr. 2014;23:867–75.View ArticleGoogle Scholar
- Reif J, Flousek J. The role of species’ ecological traits in climatically driven altitudinal range shifts of central European birds. Oikos. 2012;121:1053–60.View ArticleGoogle Scholar
- Burnham KP, Anderson DR. Model selection and multimodel inference: a practical information-theoretic approach. 2nd ed. New York: Springer; 2002.Google Scholar
- Johnson JB, Omland KS. Model selection in ecology and evolution. Trends Ecol Evol. 2004;19:101–8.View ArticlePubMedGoogle Scholar
- Bartoń K. MuMIn: multi-model inference. R package version 18.104.22.1686. http://CRAN.R-project.org/package=MuMIn. Accessed May 2016.
- Parmesan C, Yohe G. A globally coherent fingerprint of climate change impacts across natural systems. Nature. 2003;421:37–42.View ArticlePubMedGoogle Scholar
- Lenoir J, Gégout JC, Marquet PA, de Ruffray P, Brisse H. A significant upward shift in plant species optimum elevation during the 20th century. Science. 2008;320:1768–71.View ArticlePubMedGoogle Scholar
- Wolf A, Zimmerman NB, Anderegg WRL, Busby PE, Christensen J. Altitudinal shifts of the native and introduced flora of California in the context of 20th-century warming. Glob Ecol Biogeogr. 2016;25:418–29.View ArticleGoogle Scholar
- Wang Y-Z, Hu J-C. The imitatively-colored pictorial handbook of the mammals of Sichuan. 1st ed. Beijing: China Forestry Publishing House; 1999.Google Scholar
- Elsen PR, Tingley MW. Global mountain topography and the fate of montane species under climate change. Nat Clim Change. 2015;5:772–6.View ArticleGoogle Scholar
- Scherrer D, Körner C. Topographically controlled thermal-habitat differentiation buffers alpine plant diversity against climate warming. J Biogeogr. 2011;38:406–16.View ArticleGoogle Scholar
- Long RA, Bowyer RT, Porter WP, Mathewson P, Monteith KL, Kie JG. Behavior and nutritional condition buffer a large-bodied endotherm against direct and indirect effects of climate. Ecol Monogr. 2014;84:513–32.View ArticleGoogle Scholar
- Schloss CA, Nuñez TA, Lawler JJ. Dispersal will limit ability of mammals to track climate change in the Western Hemisphere. Proc Natl Acad Sci USA. 2012;109:8606–11.View ArticlePubMedPubMed CentralGoogle Scholar
- Sunday JM, Pecl GT, Frusher S, Hobday AJ, Hill N, Holbrook NJ, Edgar GJ, Stuart-Smith R, Barrett N, Wernberg T, Watson RA, Smale DA, Fulton EA, Slawinski D, Feng M, Radford BT, Thompson PA, Bates AE. Species traits and climate velocity explain geographic range shifts in an ocean-warming hotspot. Ecol Lett. 2015;18:944–53.View ArticlePubMedGoogle Scholar
- Betzholtz P-E, Pettersson LB, Ryrholm N, Franzén M. With that diet, you will go far: trait-based analysis reveals a link between rapid range expansion and a nitrogen-favoured diet. Proc R Soc Lond B Biol Sci. 2013;280:20122305.View ArticleGoogle Scholar
- Liang E-Y, Wang Y-F, Piao S-L, Lu X-M, Camarero JJ, Zhu H-F, Zhu L-P, Ellison AM, Ciais P, Peñuelas J. Species interactions slow warming-induced upward shifts of treelines on the Tibetan Plateau. Proc Natl Acad Sci USA. 2016;113:4380–5.View ArticlePubMedPubMed CentralGoogle Scholar
- Wen Z-X, Wu Y, Ge D-Y, Cheng J-L, Chang Y-B, Yang Z-S, Xia L, Yang Q-S. Data from: heterogeneous distributional responses to climate warming: evidence from rodents along a subtropical elevational gradient. Dryad Digit Repos. 2017. doi:10.5061/dryad.1q413.Google Scholar