Binckley, C. A. & Resetarits, W. J. Habitat selection determines abundance, richness and species composition of beetles in aquatic communities. Biol. Lett. 1, 370–374 (2005).
Google Scholar
Foltz, S. J. & Dodson, S. I. Aquatic Hemiptera community structure in stormwater retention ponds: A watershed land cover approach. Hydrobiologia 621, 49–62 (2009).
Google Scholar
Goldberg, F. J., Quinzio, S. & Vaira, M. Oviposition-site selection by the toad Melanophryniscus rubriventris in an unpredictable environment in Argentina. Can. J. Zool. 84, 699–705 (2006).
Google Scholar
Blaustein, L. Oviposition site selection in response to risk of predation: Evidence from aquatic habitats and consequences for population dynamics and community. In Evolutionary Theory and Processes: Modern Perspectives (ed. Wasser, S. P.) 441–456 (Kluwer, 1999).
Resetarits, W. J. & Binckley, C. A. Spatial contagion of predation risk affects colonization dynamics in experimental aquatic landscapes. Ecology 90, 869–876 (2009).
Google Scholar
Kraus, J. M. & Vonesh, J. R. Feedbacks between community assembly and habitat selection shape variation in local colonization. J. Anim. Ecol. 79, 795–802 (2010).
Google Scholar
Resetarits, W. J. Oviposition site choice and life history evolution. Am. Zool. 36, 205–215 (1996).
Google Scholar
Morris, D. W. Toward an ecological synthesis: A case for habitat selection. Oecologia 136, 1–13 (2003).
Google Scholar
Resetarits, W. J. & Wilbur, H. M. Choice of oviposition site by Hyla chrysoscelis: Role of predators and competitors. Ecology 70, 220–228 (1989).
Google Scholar
Resetarits, W. J., Binckley, C. A. & Chalcraft, D. R. Habitat selection, species interactions, and processes of community assembly in complex landscapes: A metacommunity perspective. In Metacommunities: Spatial Dynamics and Ecological Communities (eds. Holyoak, M., Leybold, A. & Holt, R. D.) 374–398 (University of Chicago Press, Chicago, 2005).
Lima, S. L. & Dill, L. M. Behavioral decisions made under the risk of predation: A review and prospectus. Can. J. Zool. 68, 619–640 (1990).
Google Scholar
Langellotto, G. A. & Denno, R. F. Responses of invertebrate natural enemies to complex-structured habitats: A meta-analytical synthesis. Oecologia 139, 1–10 (2004).
Google Scholar
Åbjörnsson, K., Brönmark, C. & Hansson, L.-A. The relative importance of lethal and non-lethal effects of fish on insect colonisation of ponds: Influence of fish on insect colonisation. Freshw. Biol. 47, 1489–1495 (2002).
Google Scholar
Pintar, M. R. & Resetarits, W. J. Jr. Out with the old, in with the new: Oviposition preference matches larval success in cope’s gray treefrog, Hyla chrysoscelis. J. Herpetol. 51, 186–189 (2017).
Google Scholar
Wellborn, G. A., Skelly, D. K. & Werner, E. E. Mechanisms creating community structure across a freshwater habitat gradient. Annu. Rev. Ecol. Evol. Syst. 27, 337–363 (1996).
Google Scholar
Caudill, C. C. & Peckarsky, B. L. Lack of appropriate behavioral or developmental responses by mayfly larvae to trout predators. Ecology 84, 2133–2144 (2003).
Google Scholar
Binckley, C. A. & Resetarits, W. J. Functional equivalence of non-lethal effects: Generalized fish avoidance determines distribution of gray treefrog, Hyla chrysoscelis, larvae. Oikos 102, 623–629 (2003).
Google Scholar
Pollard, C. J. et al. Removal of an exotic fish influences amphibian breeding site selection: Exotic fish removal. J. Wildl. Manag. 81, 720–727 (2017).
Google Scholar
Petranka, J. W. & Fakhoury, K. Evidence of a chemically-mediated avoidance response of ovipositing insects to bluegills and green frog tadpoles. Copeia 1991, 234–239 (1991).
Google Scholar
McPeek, M. A. Differential dispersal tendencies among Enallagma damselflies (Odonata) inhabiting different habitats. Oikos 56, 187–195 (1989).
Google Scholar
Šigutová, H., Šigut, M. & Dolný, A. Intensive fish ponds as ecological traps for dragonflies: An imminent threat to the endangered species Sympetrum depressiusculum (Odonata: Libellulidae). J. Insect Conserv. 19, 961–974 (2015).
Google Scholar
Potts, K. M. Survival and development of larval odonates (Anisoptera) and female oviposition site choice in response to predatory fish. https://egrove.olemiss.edu/etd/1854 (2020).
Blaustein, L., Kiflawi, M., Eitam, A., Mangel, M. & Cohen, J. E. Oviposition habitat selection in response to risk of predation in temporary pools: Mode of detection and consistency across experimental venue. Oecologia 138, 300–305 (2004).
Google Scholar
Wildermuth, H. Habitat selection and oviposition site recognition by the dragonfly Aeshna juncea (L.): An experimental approach in natural habitats (Anisoptera: Aeshnidae). Odonatologica 22, 27–44 (1993).
Wildermuth, H. Habitatselektion bei Libellen. Adv. Odonatol. 6, 223–257 (1994).
Laurila, A. Breeding habitat selection and larval performance of two anurans in freshwater rock-pools. Ecography 21, 484–494 (1998).
Google Scholar
Schwind, R. Spectral regions in which aquatic insects see reflected polarized light. J. Comp. Physiol. A 177, 439–448 (1995).
Google Scholar
Horváth, G. & Kriska, G. Polarization vision in aquatic insects and ecological traps for polarotactic insects in Aquatic Insects: Challenges to Populations (eds. Lancaster, J. & Briers, R. A.) 204–229 (CAB International Publishing, 2008).
Schulte, L. M. et al. The smell of success: Choice of larval rearing sites by means of chemical cues in a Peruvian poison frog. Anim. Behav. 81, 1147–1154 (2011).
Google Scholar
Corbet, P. S. Dragonflies: Behavior and ecology of Odonata. (Harley Books, 1999).
Nicolet, P. et al. The wetland plant and macroinvertebrate assemblages of temporary ponds in England and Wales. Biol. Conserv. 120, 261–278 (2004).
Google Scholar
Henrikson, B.-I. Sphagnum mosses as a microhabitat for invertebrates in acidified lakes and the colour adaptation and substrate preference in Leucorrhinia dubia (Odonata, Anisoptera). Ecography 16, 143–153 (1993).
Google Scholar
Kokko, H. & Sutherland, W. J. Ecological traps in changing environments: Ecological and evolutionary consequences of a behaviourally mediated Allee effect. Evol. Ecol. Res. 3, 537–551 (2001).
Gilroy, J. J. & Sutherland, W. J. Beyond ecological traps: Perceptual errors and undervalued resources. Trends Ecol. Evol. 22, 351–356 (2007).
Google Scholar
Abrams, P. A., Cressman, R. & Křivan, V. The role of behavioral dynamics in determining the patch distributions of interacting species. Am. Nat. 169, 505–518 (2007).
Google Scholar
Denton, J. & Beebee, T. J. C. Palatability of anuran eggs and embryos. Amphib. Reptil. 12, 111–112 (1991).
Google Scholar
Larson, D. J. The predaceous water beetles (Coleoptera: Dytiscidae) of Alberta: Systematics, natural history and distribution. Quaest. Entomol. 11, 245–498 (1985).
Mikolajewski, D. J. & Rolff, J. Benefits of morphological defence demonstrated by direct manipulation in larval dragonflies. Evol. Ecol. Res. 6, 619–626 (2004).
Relyea, R. A. Morphological and behavioral plasticity of larval anurans in response to different predators. Ecology 82, 523–540 (2001).
Google Scholar
Benard, M. F. Predator-induced phenotypic plasticity in organisms with complex life histories. Annu. Rev. Ecol. Evol. Syst. 35, 651–673 (2004).
Google Scholar
McCauley, S. J., Davis, C. J. & Werner, E. E. Predator induction of spine length in larval Leucorrhinia intacta (Odonata). Evol. Ecol. Res. 10, 435–447 (2008).
Nöllert, A. & Nöllert, C. Die Amphibien Europas. (Franckh-Kosmos Verlags-GmbH and Company, 1992).
Maštera, J., Zavadil, V. & Dvořák, J. Vajíčka a larvy obojživelníků České republiky. (Academia, 2015).
Speybroeck, J., Beukema, W., Bok, B. & Van der Voort, J. Field Guide to the Amphibians and Reptiles of Britain and Europe. (Bloomsbury Natural History, 2016).
Sternberg, K. & Buchwald, R. Die Libellen Baden-Württembergs. Band 2: Großlibellen (Anisoptera). (Verlag Eugen Ulmer Gmbh & Co., 2000).
Mikolajewski, D. J. & Johansson, F. Morphological and behavioral defenses in dragonfly larvae: Trait compensation and cospecialization. Behav. Ecol. 15, 614–620 (2004).
Google Scholar
Kjærstad, G., Dolmen, D., Olsvik, H. A. & Tilseth, E. The backswimmer Notonecta glauca L. (Hemiptera, Notonectidae) in Central Norway. Nor. J. Entomol. 56, 44–49 (2009).
Svensson, B. G., Tallmark, B. & Petersson, E. Habitat heterogeneity, coexistence and habitat utilization in five backswimmer species (Notonecta spp.; Hemiptera, Notonectidae). Aquat. Insects 22, 81–98 (2000).
Google Scholar
Macan, T. T. A twenty-one-year study of the water-bugs in a Moorland Fishpond. J. Anim. Ecol. 45, 913–922 (1976).
Google Scholar
Lock, K., Adriaens, T., Meutter, F. V. D. & Goethals, P. Effect of water quality on waterbugs (Hemiptera: Gerromorpha & Nepomorpha) in Flanders (Belgium): Results from a large-scale field survey. Ann. Limnol. Int. J. Limnol. 49, 121–128 (2013).
Google Scholar
Cook, W. L. & Streams, F. A. Fish predation on Notonecta (Hemiptera): Relationship between prey risk and habitat utilization. Oecologia 64, 177–183 (1984).
Google Scholar
Swevers, L., Lambert, J. G. D. & De Loof, A. Synthesis and metabolism of vertebrate-type steroids by tissues of insects: A critical evaluation. Experientia 47, 687–698 (1991).
Google Scholar
Bergsten, J. & Miller, K. B. Taxonomic revision of the Holarctic diving beetle genus Acilius Leach (Coleoptera: Dytiscidae): Acilius taxonomic revision. Syst. Entomol. 31, 145–197 (2005).
Google Scholar
Åbjörnsson, K., Wagner, B. M. A., Axelsson, A., Bjerselius, R. & Olsén, K. H. Responses of Acilius sulcatus (Coleoptera: Dytiscidae) to chemical cues from perch (Perca fluviatilis). Oecologia 111, 166–171 (1997).
Google Scholar
Boukal, D. S. et al. Catalogue of water beetles of the Czech Republic. Klapalekiana 43(Suppl.), 1–289 (2007).
Gioria, M., Schaffers, A., Bacaro, G. & Feehan, J. The conservation value of farmland ponds: Predicting water beetle assemblages using vascular plants as a surrogate group. Biol. Conserv. 143, 1125–1133 (2010).
Google Scholar
Everard, M. Britain’s Freshwater Fishes. (Princeton University Press, 2013).
Briers, R. A. & Warren, P. H. Competition between the nymphs of two regionally co-occurring species of Notonecta (Hemiptera: Notonectidae). Freshw. Biol. 42, 11–20 (1999).
Google Scholar
Wiggins, G. B., Mackay, R. J. & Smith, I. M. Evolutionary and ecological strategies of animals on annual temporary pools. Arch. Für Hydrobiol. Suppl. 58, 197–206 (1980).
Culler, L. E., Ohba, S. & Crumrine, P. Predator-Prey Interactions of Dytiscids. In Ecology, Systematics, and the Natural History of Predaceous Diving Beetles (Coleoptera: Dytiscidae) (ed. Yee, D. A.) 363–379 (Springer, 2014).
Schuh, R. T. & Slater, J. A. True Bugs of the World (Hemiptera:Heteroptera): Classification and Natural History (Cornell University Press, Cornell, 1995).
Streams, F. A. Intrageneric predation by Notonecta (Hemiptera: Notonectidae) in the laboratory and in nature. Ann. Entomol. Soc. Am. 85, 265–273 (1992).
Google Scholar
Giacoma, C., Zugolaro, C. & Beani, L. The advertisement calls of the green toad (Bufo viridis): Variability and role in mate choice. Herpetologica 53, 454–464 (1997).
Pekár, S. & Brabec, M. Generalized estimating equations: A pragmatic and flexible approach to the marginal GLM modelling of correlated data in the behavioural sciences. Ethology 124, 86–93 (2018).
Google Scholar
Halekoh, U., Højsgaard, S. & Yan, J. The R Package geepack for generalized estimating equations. J. Stat. Softw. 15, 1–11 (2006).
Google Scholar
R Core Team. R: A Language and Environment for Statistical Computing (The R Foundation for Statistical Computing, Vienna, Austria). https://www.r-project.org/ (2020).
Wells, K. D. The Ecology and Behavior of Amphibians. (University of Chicago Press, 2007).
Purrenhage, J. L. & Boone, M. D. Amphibian community response to variation in habitat structure and competitor density. Herpetologica 65, 14–30 (2009).
Google Scholar
Formanowicz, D. R. & Bobka, M. S. Predation risk and microhabitat preference: An experimental study of the behavioral responses of prey and predator. Am. Midl. Nat. 121, 379–386 (1989).
Google Scholar
Egan, R. S. & Paton, P. W. C. Within-pond parameters affecting oviposition by wood frogs and spotted salamanders. Wetlands 24, 1–13 (2004).
Google Scholar
Ward, S. A. Optimal habitat selection in time-limited dispersers. Am. Nat. 129, 568–579 (1987).
Google Scholar
Fretwell, S. D. & Lucas, H. L. On territorial behavior and other factors influencing habitat distribution in birds. I. Theoretical development. Biotheoretica 19, 16–36 (1970).
Google Scholar
Austad, S. N. A classification of alternative reproductive behaviors and methods for field-testing ESS models. Am. Zool. 24, 309–319 (1984).
Google Scholar
Crespo, J. G. A review of chemosensation and related behavior in aquatic insects. J. Insect Sci. 11, 1–39 (2011).
Google Scholar
Wildermuth, H. Dragonflies recognize the water of rendezvous and oviposition sites by horizontally polarized light: A behavioural field test. Naturwissenschaften 85, 297–302 (1998).
Google Scholar
Chislock, M. F., Doster, E., Zitomer, R. A. & Wilson, A. E. Eutrophication: Causes, consequences, and controls in aquatic ecosystems. Nat. Educ. Knowl. 4, 10 (2013).
Dolný, A., Mižičová, H. & Harabiš, F. Natal philopatry in four European species of dragonflies (Odonata: Sympetrinae) and possible implications for conservation management. J. Insect Conserv. 17, 821–829 (2013).
Google Scholar
Refsnider, J. M. & Janzen, F. J. Putting eggs in one basket: Ecological and evolutionary hypotheses for variation in oviposition-site choice. Annu. Rev. Ecol. Evol. Syst. 41, 39–57 (2010).
Google Scholar
Brodin, T., Mikolajewski, D. J. & Johansson, F. Behavioural and life history effects of predator diet cues during ontogeny in damselfly larvae. Oecologia 148, 162–169 (2006).
Google Scholar
Kershenbaum, A., Spencer, M., Blaustein, L. & Cohen, J. E. Modelling evolutionarily stable strategies in oviposition site selection, with varying risks of predation and intraspecific competition. Evol. Ecol. 26, 955–974 (2012).
Google Scholar
Hopper, K. R. Risk-spreading and bet-hedging in insect population biology. Annu. Rev. Entomol. 44, 535–560 (1999).
Google Scholar
Gioria, M. Habitats. In Ecology, Systematics, and the Natural History of predaceous diving beetles (Coleoptera: Dytiscidae) (ed. Yee, D. A.) 307–362 (Springer, Netherlands, 2014).
Diehl, S. Fish predation and benthic community structure: The role of omnivory and habitat complexity. Ecology 73, 1646–1661 (1992).
Google Scholar
Giller, P. S. & McNeill, S. Predation strategies, resource partitioning and habitat selection in Notonecta (Hemiptera/Heteroptera). J. Anim. Ecol. 50, 789–808 (1981).
Google Scholar
Ribera, I. & Nilsson, A. N. Morphometric patterns among diving beetles (Coleoptera: Noteridae, Hygrobiidae, and Dytiscidae). Can. J. Zool. 73, 2343–2360 (2011).
Google Scholar
Roberts, G. Why individual vigilance declines as group size increases. Anim. Behav. 51, 1077–1086 (1996).
Google Scholar
Schoeppner, N. M. & Relyea, R. A. Damage, digestion, and defence: The roles of alarm cues and kairomones for inducing prey defences. Ecol. Lett. 8, 505–512 (2005).
Google Scholar
Schoeppner, N. M. & Relyea, R. A. Interpreting the smells of predation: How alarm cues and kairomones induce different prey defences. Funct. Ecol. 23, 1114–1121 (2009).
Google Scholar
McCauley, S. J. & Rowe, L. Notonecta exhibit threat-sensitive, predator-induced dispersal. Biol. Lett. 6, 449–452 (2010).
Google Scholar
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