Li, J. & Thompson, D. W. Widespread changes in surface temperature persistence under climate change. Nature 599(7885), 425–430. https://doi.org/10.1038/s41586-021-03943-z (2021).
Google Scholar
Raftery, A. E., Zimmer, A., Frierson, D. M., Startz, R. & Liu, P. Less than 2 °C warming by 2100 unlikely. Nat. Clim. Change 7, 637–641 (2017).
Google Scholar
Olabi, A. G. et al. Assessment of the pre-combustion carbon capture contribution into sustainable development goals SDGs using novel indicators. Renew. Sustain. Energy Rev. 153, 111710. https://doi.org/10.1016/j.rser.2021.111710 (2022).
Google Scholar
Badino, G. Cave temperatures and global climatic change. Int. J. Speleol. 33(1), 103–114 (2004).
Wang, J. et al. Recent global decline in endorheic basin water storages. Nat. Geosci. 11(12), 926–932 (2018).
Google Scholar
Figura, S., Livingstone, D. M., Hoehn, E. & Kipfer, R. Regime shift in groundwater temperature triggered by the Arctic Oscillation. Geophys. Res. Lett. 38(23), 401–405 (2011).
Mueller, M. H., Huggenberger, P. & Epting, J. Combining monitoring and modelling tools as a basis for city-scale concepts for a sustainable thermal management of urban groundwater resources. Sci. Total Environ. 627, 1121–1136 (2018).
Google Scholar
Taylor, C. A. & Stefan, H. G. Shallow groundwater temperature response to climate change and urbanization. J. Hydrol. 375, 601–612 (2009).
Google Scholar
Dehghani, R., Poudeh, H. T. & Izadi, Z. The effect of climate change on groundwater level and its prediction using modern meta-heuristic model. Ground. Sustain. Dev. 16, 100702. https://doi.org/10.1016/j.gsd.2021.100702 (2022).
Lenton, T. M. et al. Climate tipping points—Too risky to bet against. Nature 57, 592–595 (2019).
Google Scholar
Albert, J. S. et al. Scientists’ warning to humanity on the freshwater biodiversity crisis. Ambio 50(1), 85–94 (2021).
Google Scholar
Stein, H. et al. Stygoregions—A promising approach to a bioregional classification of groundwater systems. Sci. Rep. 2, 673. https://doi.org/10.1038/srep00673 (2012).
Google Scholar
Baković, N., Matoničkin Kepčija, R. & Siemensma, F. J. Transitional and small aquatic cave habitats diversification based on protist assemblages in the Veternica cave (Medvednica Mt., Croatia). Subterr. Biol. 42, 43–60 (2022).
Magnabosco, C. et al. The biomass and biodiversity of the continental subsurface. Nat. Geosci. 11(10), 707–717 (2018).
Google Scholar
Chen, Z. et al. The World Karst Aquifer Mapping project: Concept, mapping procedure and map of Europe. Hydrogeol. J. 25, 771–785 (2017).
Google Scholar
Eme, D. et al. Do cryptic species matter in macroecology? Sequencing European groundwater crustaceans yields smaller ranges but does not challenge biodiversity determinants. Ecography 41(2), 424–436 (2018).
Manenti, R. et al. The stenoendemic cave-dwelling planarians (Platyhelminthes, Tricladida) of the Italian Alps and Apennines: conservation issues. J. Nat. Conserv. 45, 90–97 (2018).
Zagmajster, M., Malard, F., Eme, D. & Culver, D. C. Subterranean biodiversity patterns from global to regional scales. In Cave Ecology, Ecological Studies—Analysis and Synthesis (eds Moldovan, O. et al.) 19–227 (Springer, 2018).
Hose, G. C. et al. Invertebrate traits, diversity and the vulnerability of groundwater ecosystems. Funct. Ecol. 36, 2200. https://doi.org/10.1111/1365-2435.14125 (2022).
Google Scholar
Angilletta, M. J. Jr. & Angilletta, M. J. Thermal Adaptation: A Theoretical and Empirical Synthesis (Oxford University Press, 2009).
Pallarées, S. et al. Loss of heat acclimation capacity could leave subterranean specialists highly sensitive to climate change. Anim. Conserv. 24(3), 482–490 (2020).
Vasseur, D. A. et al. Increased temperature variation poses a greater risk to species than climate warming. Proc. R. Soc. B 281, 20132612. https://doi.org/10.1098/rspb.2013.2612 (2014).
Google Scholar
Castaño-Sánchez, A., Hose, G. C. & Reboleira, A. S. P. Ecotoxicological effects of anthropogenic stressors in subterranean organisms: A review. Chemosphere 244, 125422. https://doi.org/10.1016/j.chemosphere.2019.125422 (2020).
Google Scholar
Castaño-Sánchez, A., Hose, G. C. & Reboleira, A. S. P. Salinity and temperature increase impact groundwater crustaceans. Sci. Rep. 10(1), 1–9 (2020).
Issartel, J., Hervant, F., Voituron, Y., Renault, D. & Vernon, P. Behavioural, ventilatory and respiratory responses of epigean and hypogean crustaceans to different temperatures. Comp. Biochem. Physiol. Mol. Amp Integr. Physiol. 141, 1–7 (2005).
Issartel, J., Voituron, Y. & Hervant, F. Impact of temperature on the survival, the activity and the metabolism of the cave-dwelling Niphargus virei, the ubiquitous stygobiotic N. rhenorhodanensis and the surface-dwelling Gammarus fossarum (Crustacea, Amphipoda). Subterr. Biol. 5, 9–14 (2007).
Mermillod-Blondin, F. et al. Thermal tolerance breadths among groundwater crustaceans living in a thermally constant environment. J. Exp. Biol. 216, 1683–1694 (2013).
Google Scholar
Di Lorenzo, T. et al. Metabolic rates of a hypogean and an epigean species of copepod in an alluvial aquifer. Freshw. Biol. 60, 426–435 (2015).
Di Lorenzo, T. & Galassi, D. M. P. Effect of temperature rising on the stygobitic crustacean species Diacyclops belgicus: Does global warming affect groundwater populations? Water 9, 951. https://doi.org/10.3390/w9120951 (2017).
Google Scholar
Mammola, S. et al. Climate change going deep: The effects of global climatic alterations on cave ecosystems. Anthr. Rev. 6(1–2), 98–116 (2019).
Jones, K. et al. The critical thermal maximum of diving beetles (Coleoptera: Dytiscidae): A comparison of subterranean and surface-dwelling species. Curr. Opin. Insect. Sci. 1, 100019 (2021).
Pörtner, H. O. Physiological basis of temperature-dependent biogeography: Trade-offs in muscle design and performance in polar ectotherms. J. Exp. Biol. 205, 2217–2230 (2022).
Clarke, A. & Fraser, K. P. P. Why does metabolism scale with temperature? Funct. Ecol. 18, 243–251 (2004).
Dell, A. I., Pawar, S. & Savage, V. M. Systematic variation in the temperature dependence of physiological and ecological traits. Proc. Natl. Acad. Sci. 108, 10591–10596 (2011).
Google Scholar
Willmer, P., Stone, G. & Johnston, I. Environmental Physiology of Animals (Wiley, 2009).
Gillooly, J. F., Brown, J. H., West, G. B., Savage, V. M. & Charnov, E. L. Effects of size and temperature on metabolic rate. Science 293, 2248–2251 (2001).
Google Scholar
Gillooly, J. F., Charnov, E. L., West, G. B., Savage, V. M. & Brown, J. H. Effects of size and temperature on developmental time. Nature 417, 70–73 (2002).
Google Scholar
Hervant, F., Mathieu, J., Barré, H., Simon, K. & Pinon, C. Comparative study on the behavioural, ventilatory, and respiratory responses of hypogean and epigean crustaceans to long-term starvation and subsequent feeding. Comp. Biochem. Physiol. B 118A, 1277–1283 (1997).
Google Scholar
Wilhelm, F. M., Taylor, S. J. & Adams, G. L. Comparison of routine metabolic rates of the stygobite, Gammarus acherondytes (Amphipoda: Gammaridae) and the stygophile, Gammarus troglophilus. Freshwat. Biol. 51, 1162–1174 (2006).
Reboleira, A. S. P. S., Borges, P., Gonçalves, F., Serrano, A. R. M. & Oromí, P. The subterranean fauna of a biodiversity hotspot region—Portugal: An overview and its conservation. Int. J. Speleol. 40(1), 23–37 (2011).
Reboleira, A. S. P. S., Abrantes, N., Oromí, P. & Gonçalves, F. J. M. Acute toxicity of copper sulfate and potassium dichromate on stygobiont Proasellus: General aspects of groundwater ecotoxicology and future perspectives. Water Air Soil Pollut. 224, 1550. https://doi.org/10.1007/s11270-013-1550-0 (2013).
Google Scholar
Morvan, C. et al. Timetree of Aselloidea reveals species diversification dynamics in groundwater. Syst. Biol. 62(4), 512–522 (2013).
Google Scholar
Castaño-Sánchez, A., Malard, F., Kalčikova, G. & Reboleira, A. S. P. S. Novel protocol for acute in situ ecotoxicity test using native crustaceans applied to groundwater ecosystems. Water 13(8), 1132. https://doi.org/10.3390/w13081132 (2021).
Google Scholar
Di Lorenzo, T. et al. Recommendations for ecotoxicity testing with stygobiotic species in the framework of groundwater environmental risk assessment. Sci. Total Environ. 681(1), 292–304 (2019).
Google Scholar
Rezende, E. L., Tejedo, M. & Santos, M. Estimating the adaptative potential of critical thermal limits: Methodological problems and evolutionary implications. Funct. Ecol. 25, 111–121 (2011).
Schneider, C. A., Rasband, W. S. & Eliceiri, K. W. NIH Image to ImageJ: 25 years of image analysis. Nat. Methods 9(7), 671–675 (2012).
Google Scholar
Anderson, M. J. A new method for non-parametric multivariate analysis of variance. Austral Ecol. 26, 32–46 (2001).
Harvey, P. H. & Pagel, M. D. The Comparative Method in Evolutionary Biology (Oxford University Press, 1991).
Dodds, P. S., Rothman, D. H. & Weitz, J. S. Re-examination of the “3/4” law of metabolism. J. Theor. Biol. 209, 9–27 (2001).
Google Scholar
Manly, B. F. J. Randomization, Bootstrap and Monte Carlo Methods in Biology (Chapman & Hall/CRC Press, 2006).
Google Scholar
R Core Team. R: A Language and Environment for Statistical Computing. https://www.R-project.org/ (R Foundation for Statistical Computing, Vienna, Austria, 2018).
Simčič, T. & Sket, B. Comparison of some epigean and troglobiotic animals regarding their metabolism intensity. Examination of a classical assertion. Int. J. Speleol. 48, 133–144 (2019).
Hazell, S. P., Pedersen, B. P., Worland, M. R., Blackburn, T. M. & Bale, J. S. A method for the rapid measurement of thermal tolerance traits in studies of small insects. Physiol. Entomol. 33(4), 389–394 (2008).
Cohen, J. M., Lajeunesse, M. J. & Rohr, J. R. A global synthesis of animal phenological responses to climate change. Nat. Clim. Change 8, 224. https://doi.org/10.1038/s41558-018-0067-3 (2018).
Google Scholar
Ficetola, G. F., Lunghi, E. & Manenti, R. Microhabitat analyses support relationships between niche breadth and range size when spatial autocorrelation is strong. Ecography 43(5), 724–734 (2020).
Sánchez-Fernández, D., Rizzo, V. & Bourdeau, C. The deep subterranean environment as a model system in ecological, biogeographical and evolutionary research. Subterr. Biol. 25, 1–7 (2018).
Pallarés, S. et al. Loss of heat acclimation capacity could leave subterranean specialists highly sensitive to climate change. Anim. Conserv. 24(3), 482–490 (2021).
Google Scholar
Griebler, C. & Avramov, M. Groundwater ecosystem services: A review. Freshw. Sci. 34(1), 355–367 (2015).
Saccò, M. et al. Stygofaunal diversity and ecological sustainability of coastal groundwater ecosystems in a changing climate: The Australian paradigm. Freshw. Biol. https://doi.org/10.1111/fwb.13987 (2022).
Ikeda, T., Kanno, Y., Ozaki, K. & Shinada, A. Metabolic rates of epipelagic marine copepods as a function of body mass and temperature. Mar. Biol. 139, 587–596 (2001).
Mezek, T., Simčič, T., Arts, M. T. & Brancelj, A. Effect of fasting on hypogean (Niphargus stygius) and epigean (Gammarus fossarum) amphipods: A laboratory study. Aquat. Ecol. 44(2), 397–408 (2010).
Google Scholar
Hüppop, K. The role of metabolism in the evolution of cave animals. NSS Bulletin 47, 136–146 (1985).
Humphreys, W. F. Hydrogeology and groundwater ecology: Does each inform the other? Hydrogeol. J. 17(1), 5–21 (2009).
Google Scholar
Glazier, D. S. The 3/4-power law is not universal: Evolution of isometric, ontogenetic metabolic scaling in pelagic animals. Bioscience 56(4), 325–332 (2006).
Sánchez-Fernández, D., Galassi, D. M. P., Wynne, J. J., Cardoso, P. & Mammola, S. Don’t forget subterranean ecosystems in climate change agendas. Nat. Clim. Change 11, 458–459 (2021).
Google Scholar
Reboleira, A. S. P. S. et al. Nutrient-limited subarctic caves harbour more diverse and complex bacterial communities than their surface soil. Environ. Microbiome 17, 41 (2022).
Google Scholar
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