Chase, J. M. et al. The interaction between predation and competition: A review and synthesis. Ecol. Lett. 5, 302–315. https://doi.org/10.1046/j.1461-0248.2002.00315.x (2002).
Google Scholar
Droge, E., Creel, S., Becker, M. S. & M’Soka, J. Risky times and risky places interact to affect prey behaviour. Nat. Ecol. Evol. 1, 1123–1128. https://doi.org/10.1038/s41559-017-0220-9 (2017).
Google Scholar
Allesina, S. & Levine Jonathan, M. A competitive network theory of species diversity. Proc. Natl. Acad. Sci. U.S.A. 108, 5638–5642. https://doi.org/10.1073/pnas.1014428108 (2011).
Google Scholar
Bairey, E., Kelsic, E. D. & Kishony, R. High-order species interactions shape ecosystem diversity. Nat. Commun. 7, 12285. https://doi.org/10.1038/ncomms12285 (2016).
Google Scholar
Letten, A. D. & Stouffer, D. B. The mechanistic basis for higher-order interactions and non-additivity in competitive communities. Ecol. Lett. 22, 423–436. https://doi.org/10.1111/ele.13211 (2019).
Google Scholar
Lotka, A. J. Elements of physical biology. Sci. Prog. Twent. Century (1919–1933) 21, 341–343 (1926).
Volterra, V. Variazioni e Fluttuazioni del Numero d’Individui in Specie Animali Conviventi. (Società Anonima Tipografica “Leonardo da Vinci”, 1926).
Schmitz, O. J. Top predator control of plant biodiversity and productivity in an old-field ecosystem. Ecol. Lett. 6, 156–163. https://doi.org/10.1046/j.1461-0248.2003.00412.x (2003).
Google Scholar
Fey, K., Banks, P. B., Oksanen, L. & Korpimäki, E. Does removal of an alien predator from small islands in the Baltic Sea induce a trophic cascade?. Ecography 32, 546–552. https://doi.org/10.1111/j.1600-0587.2008.05637.x (2009).
Google Scholar
Terborgh John, W. Toward a trophic theory of species diversity. Proc. Natl. Acad. Sci. U.S.A. 112, 11415–11422. https://doi.org/10.1073/pnas.1501070112 (2015).
Google Scholar
Pringle, R. M. et al. Predator-induced collapse of niche structure and species coexistence. Nature 570, 58–64. https://doi.org/10.1038/s41586-019-1264-6 (2019).
Google Scholar
Sandom, C. et al. Mammal predator and prey species richness are strongly linked at macroscales. Ecology 94, 1112–1122. https://doi.org/10.1890/12-1342.1 (2013).
Google Scholar
Louette, G. & De Meester, L. Predation and priority effects in experimental zooplankton communities. Oikos 116, 419–426. https://doi.org/10.1111/j.2006.0030-1299.15381.x (2007).
Google Scholar
Johnston, N. K., Pu, Z. & Jiang, L. Predator identity influences metacommunity assembly. J. Anim. Ecol. 85, 1161–1170. https://doi.org/10.1111/1365-2656.12551 (2016).
Google Scholar
Karakoc, C., Radchuk, V., Harms, H. & Chatzinotas, A. Interactions between predation and disturbances shape prey communities. Sci. Rep. 8, 2968. https://doi.org/10.1038/s41598-018-21219-x (2018).
Google Scholar
Hubbell, S. P. The Unified Neutral Theory of Biodiversity and Biogeography (MPB-32) (Princeton University Press, 2011).
Google Scholar
MacArthur, R. H. & Wilson, E. O. The Theory of Island Biogeography (Princeton University Press, 2001).
Google Scholar
Daniel, J., Gleason, J. E., Cottenie, K. & Rooney, R. C. Stochastic and deterministic processes drive wetland community assembly across a gradient of environmental filtering. Oikos 128, 1158–1169. https://doi.org/10.1111/oik.05987 (2019).
Google Scholar
Lehner, B. & Döll, P. Development and validation of a global database of lakes, reservoirs and wetlands. J. Hydrol. 296, 1–22. https://doi.org/10.1016/j.jhydrol.2004.03.028 (2004).
Google Scholar
Chase, J. M., Biro, E. G., Ryberg, W. A. & Smith, K. G. Predators temper the relative importance of stochastic processes in the assembly of prey metacommunities. Ecol. Lett. 12, 1210–1218. https://doi.org/10.1111/j.1461-0248.2009.01362.x (2009).
Google Scholar
Werner, E. E. & Peacor, S. D. A review of trait-mediated indirect interactions in ecological communities. Ecology 84, 1083–1100. https://doi.org/10.1890/0012-9658(2003)084[1083:AROTII]2.0.CO;2 (2003).
Google Scholar
Pearson, D. E., Ortega, Y. K., Eren, Ö. & Hierro, J. L. Community assembly theory as a framework for biological invasions. Trends Ecol. Evol. 33, 313–325. https://doi.org/10.1016/j.tree.2018.03.002 (2018).
Google Scholar
Duchesne, É. et al. Variable strength of predator-mediated effects on species occurrence in an arctic terrestrial vertebrate community. Ecography 44, 1236–1248. https://doi.org/10.1111/ecog.05760 (2021).
Google Scholar
Ryberg, W. A., Smith, K. G. & Chase, J. M. Predators alter the scaling of diversity in prey metacommunities. Oikos 121, 1995–2000. https://doi.org/10.1111/j.1600-0706.2012.19620.x (2012).
Google Scholar
Carrete Vega, G. & Wiens, J. J. Why are there so few fish in the sea?. Proc. R. Soc. B 279, 2323–2329. https://doi.org/10.1098/rspb.2012.0075 (2012).
Google Scholar
Barrett, M. et al. Living planet report 2018: Aiming higher. (2018).
Reid, A. J. et al. Emerging threats and persistent conservation challenges for freshwater biodiversity. Biol. Rev. 94, 849–873. https://doi.org/10.1111/brv.12480 (2019).
Google Scholar
Di Marco, M. et al. Changing trends and persisting biases in three decades of conservation science. Glob. Ecol. Conserv. 10, 32–42. https://doi.org/10.1016/j.gecco.2017.01.008 (2017).
Google Scholar
Hammerschlag, N. et al. Ecosystem function and services of aquatic predators in the anthropocene. Trends Ecol. Evol. 34, 369–383. https://doi.org/10.1016/j.tree.2019.01.005 (2019).
Google Scholar
Wang, T. et al. Amur tigers and leopards returning to China: direct evidence and a landscape conservation plan. Landsc Ecol 31, 491–503. https://doi.org/10.1007/s10980-015-0278-1 (2016).
Google Scholar
Hong, S. et al. Stream health, topography, and land use influences on the distribution of the Eurasian otter Lutra lutra in the Nakdong River basin, South Korea. Ecol. Indic. 88, 241–249. https://doi.org/10.1016/j.ecolind.2018.01.004 (2018).
Google Scholar
Guter, A., Dolev, A., Saltz, D. & Kronfeld-Schor, N. Using videotaping to validate the use of spraints as an index of Eurasian otter (Lutra lutra) activity. Ecol. Indic. 8, 462–465. https://doi.org/10.1016/j.ecolind.2007.04.009 (2008).
Google Scholar
Sittenthaler, M., Bayerl, H., Unfer, G., Kuehn, R. & Parz-Gollner, R. Impact of fish stocking on Eurasian otter (Lutra lutra) densities: A case study on two salmonid streams. Mamm. Biol. 80, 106–113. https://doi.org/10.1016/j.mambio.2015.01.004 (2015).
Google Scholar
Zheng, B., Huang, H., Zhang, Y. & Dai, D. The Fishes of Tumen River (Jilin People’s Publishing House, 1980).
Fleishman, E., Murphy, D. D. & Brussard, P. F. A new method for selection of umbrella species for conservation planning. Ecol Appl 10, 569–579. https://doi.org/10.1890/1051-0761(2000)010[0569:ANMFSO]2.0.CO;2 (2000).
Google Scholar
Roberge, J.-M. & Angelstam, P. E. R. Usefulness of the umbrella species concept as a conservation tool. Conserv. Biol. 18, 76–85. https://doi.org/10.1111/j.1523-1739.2004.00450.x (2004).
Google Scholar
McGowan, J. et al. Conservation prioritization can resolve the flagship species conundrum. Nat. Commun. 11, 994. https://doi.org/10.1038/s41467-020-14554-z (2020).
Google Scholar
Katano, I., Doi, H., Eriksson, B. K. & Hillebrand, H. A cross-system meta-analysis reveals coupled predation effects on prey biomass and diversity. Oikos 124, 1427–1435. https://doi.org/10.1111/oik.02430 (2015).
Google Scholar
Leibold, M. A. A graphical model of keystone predators in food webs: Trophic regulation of abundance, incidence, and diversity patterns in communities. Am. Nat. 147, 784–812. https://doi.org/10.1086/285879 (1996).
Google Scholar
McPeek, M. A. The consequences of changing the top predator in a food web: A comparative experimental approach. Ecol. Monogr. 68, 1–23. https://doi.org/10.1890/0012-9615(1998)068[0001:TCOCTT]2.0.CO;2 (1998).
Google Scholar
Chase, J. M. & Leibold, M. A. Ecological Niches: Linking Classical and Contemporary Approaches (University of Chicago Press, 2003).
Google Scholar
Gravel, D., Canham, C. D., Beaudet, M. & Messier, C. Reconciling niche and neutrality: The continuum hypothesis. Ecol. Lett. 9, 399–409. https://doi.org/10.1111/j.1461-0248.2006.00884.x (2006).
Google Scholar
Yoshida, T., Jones, L. E., Ellner, S. P., Fussmann, G. F. & Hairston, N. G. Rapid evolution drives ecological dynamics in a predator–prey system. Nature 424, 303–306. https://doi.org/10.1038/nature01767 (2003).
Google Scholar
Yin, X., Wang, J., Yin, H. & Ruan, Y. Does inducible defense mitigate physiological stress responses of prey to predation risk?. Hydrobiologia 843, 173–181. https://doi.org/10.1007/s10750-019-04046-7 (2019).
Google Scholar
Chalcraft, D. R. & Resetarits, W. J. Jr. Predator identity and ecological impacts: Functional redundancy or functional diversity?. Ecology 84, 2407–2418. https://doi.org/10.1890/02-0550 (2003).
Google Scholar
Petchey, O. L. & Gaston, K. J. Functional diversity: Back to basics and looking forward. Ecol. Lett. 9, 741–758. https://doi.org/10.1111/j.1461-0248.2006.00924.x (2006).
Google Scholar
Burner, R. C. et al. Functional structure of European forest beetle communities is enhanced by rare species. Biol. Conserv. 267, 109491. https://doi.org/10.1016/j.biocon.2022.109491 (2022).
Google Scholar
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