, Volume 92, Issue 2, pp 162–165 | Cite as

Predator induced life-history shifts in a freshwater cladoceran

  • Herwig Stibor
Original Papers


Life-history theory predicts that maturity and resource allocation patterns are highly sensitive to selective predation. Under reduced adult survival, selection will favour genotypes capable of reproducing earlier, at a smaller size and with a higher reproductive effort. When exposed to water that previously held fish, (size selective predators which prefer larger Daphnia), individuals of Daphnia hyalina reproduced earlier, at a smaller size and had a higher reproductive investment. Hence the prey was able to switch its life history pattern in order to become less susceptible to predation by a specific predator. The cue that evokes the prey response is a chemical released by the predator.

Key words

Daphnia Predator induction Life-history strategy Resource allocation Phenotypic plasticity 


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  1. Brett MT (1992) Chaoborus and fish mediated influences on Daphnia longispina population structure, dynamics and life history strategies. Oecologia 89: 69–77Google Scholar
  2. Bull JJ (1987) Evolution of phenotypic variance. Evolution 41: 303–315Google Scholar
  3. Campbell CE (1991) Prey selectivity of threespine sticklebacks (Gasterosteus aculeatus) and phantom midge larvae (Chaoborus spp.) in Newfoundland lakes. Fresh Biol 25: 155–167Google Scholar
  4. Caswell H (1989) Life-history strategies. In: Cherret JM (ed) Ecological Concepts: The contribution of ecology to an understanding of the natural world. (Symp Brit Ecol Soc 29) Blackwell, London, pp 285–307Google Scholar
  5. Charlesworth B (1980) Evolution in Age Structured Populations. Cambridge University Press, New YorkGoogle Scholar
  6. Crowl TA, Covich AP (1990) Fredator induced life-history shifts in a freshwater snail. Science 247: 949–951Google Scholar
  7. Dangerfield JM, Hassall M (1992) Phenotypic variation in the breeding phenology of the woodlouse Armadillidium vulgare. Oecologia 89: 140–146Google Scholar
  8. Dodson SI (1988a) Cyclomorphosis in Daphnia galeata mendotae Birge and D. retrocurva as a predator induced response. Freshw Biol 19: 109–114Google Scholar
  9. Dodson SI (1988b) The ecological role of chemical stimuli for the zooplankton: predator-avoidance behavior in Daphnia. Limnol Oceanogr 33: 1431–1439Google Scholar
  10. Dodson SI (1989) The ecological role of chemical stimuli for the zooplankton: predator-induced morphology in Daphnia. Oecologia 78: 361–367Google Scholar
  11. Eggers DM (1982) Planktivore preference by prey size. Ecology 63: 381–390Google Scholar
  12. Gabriel W, Taylor BE (1991) Optimal resource allocation in cladocerans. Int Ver Theor Angew Limnol Verh 24: 2784–2787Google Scholar
  13. Gadgil M, Bossert PW (1970) Life historical consequences of natural selection. Am Nat 104: 1–24Google Scholar
  14. Hanazato T (1991) Effects of a Chaoborus released chemical on Daphnia ambigua: Reduction in the tolerance of the Daphnia to summer water temperature. Limnol Oceanogr 36: 165–172Google Scholar
  15. Havel JE (1987) Predator-induced defenses: A review. In: Kerfoot WC, Sih A (eds) Predation: Direct and indirect impacts on aquatic communities. University Press of New England, Hanover, NH, pp 263–278Google Scholar
  16. Jachner A (1988) Density and feeding activity of planktivorous fish. Wiad ekol 34: 143–157Google Scholar
  17. Kerfoot WC (1980) Perspectives on Cyclomorphosis: Separation of Phenotypes and Genotypes. In: Kerfoot WC (ed) Evolution and Ecology of Zooplankton Communities. University Press of New England, Hanover, NH, pp 470–496Google Scholar
  18. Kozlowski J, Wiegert RG (1987) Optimal age and size at maturity in annuals and perennials with determinate growth. Evol Ecol 1: 231–244Google Scholar
  19. Lampert W (1988) The relative importance of food limitation and predation in the seasonal cycle of two Daphnia species. Verh Internat Ver Limnol 23: 713–718Google Scholar
  20. Lampert W, Wolf HG (1986) Cyclomorphosis in Daphnia cucullata: morphometric and population genetic analyses. J Plankton Res 8: 289–303Google Scholar
  21. Law R (1979) Optimal life-histories under age-specific predation. Am Nat 114: 399–417Google Scholar
  22. Levins R (1968) Evolution in Changing Environments. Princeton University Press, PrincetonGoogle Scholar
  23. Loose JC (1992) Daphnia diel vertical migration behavior: response to vertebrate predator abundance. Arch Hydrobiol Beih Erg (in press)Google Scholar
  24. Lynch M, Weider L, Lampert W (1986) Measurement of the carbon balance in Daphnia. Limnol Oceanogr 31: 17–33Google Scholar
  25. Machacek J (1991) Indirect effect of planktivorous fish on the growth and reproduction of Daphnia galeata. Hydrobiologia 225: 193–197Google Scholar
  26. Michod RE (1979) Evolution of life-histories in response to age specific mortality factors. Am Nat 113: 531–550Google Scholar
  27. Pace ML, Porter KG, Feig YS (1984) Life history variation within a parthenogenetic population of Daphnia parvula. Oecologia 63: 43–51Google Scholar
  28. Pijanowska J (1992) Diel vertical migration in zooplankton: fixed or inducible behavior? Arch Hydrobiol Beih Erg (in press)Google Scholar
  29. Reznik AD, Bryga H, Endler JA (1990) Experimentally induced life-history evolution in a natural population. Nature 46: 357–359Google Scholar
  30. Ringelberg J (1991) A mechanism of predator mediated induction of diel vertical migration in Daphnia hyalina. J Plankton Res 13: 83–89Google Scholar
  31. Semlitsch RD, Wilbur HM (1989) Artificial selection for paedomorphosis in the salamander Ambystoma talpoideum. Evolution 43: 105–112Google Scholar
  32. Spitze K (1991) Chaoborus predation and life-history evolution in Daphnia pulex: temporal pattern of population diversity, fitness, and mean life history. Evolution 45: 82–92Google Scholar
  33. Stearns SC, Koella JC (1986) The evolution of phenotypic plasticity in life-history traits: predictions of reaction norms for age and size at maturity. Evolution 40: 893–913Google Scholar
  34. Stibor H (1991) Größenvariabilität von Daphnia spp. bei der ersten Reproduktion. Diplom-thesis, Universität KielGoogle Scholar
  35. Taylor BE, Gabriel W (1992) To grow or not to grow: Optimal resource allocation for Daphnia. Am Nat 139: 248–266Google Scholar
  36. Tollrian R (1990) Predator induced helmet formation in Daphnia cucullata Sars. Arch Hydrobiol 119: 191–196Google Scholar
  37. Townsend CR, Winfield JJ, Parson G, Cryer M (1986) The response of young roach Rutilus rutilus to seasonal changes in abundance of microcrustacean prey: A field demonstration of switching. Oikos 46: 372–378Google Scholar
  38. Vanni MJ (1987) Indirect effect of predators on age-structured prey populations: planktivorous fish and zooplankton. In: Kerfoot WC, Sih A (eds) Predation: Direct and indirect impacts on aquatic communities. New England Press, Hanover, New Hampshire, pp 149–160Google Scholar
  39. Vuorinen I, Ketola M, Walls M (1989) Defensive spine formation in Daphnia pulex Leydig and induction by Chaoborus crystallinus De Geer. Limnol Oceanogr 34: 245–248Google Scholar
  40. Walls M, Ketola M (1989) Effects of predator-induced spines on individual fitness in Daphnia pulex. Limnol Oceanogr 34: 390–396Google Scholar
  41. Wilbur HM, Collins JP (1973) Ecological aspects of amphibian metamorphosis. Science 182: 1305–1314Google Scholar
  42. Zaret TM (1980) Predation and freshwater communities. Yale University Press, New Haven, LondonGoogle Scholar

Copyright information

© Springer-Verlag 1992

Authors and Affiliations

  • Herwig Stibor
    • 1
  1. 1.Max-Planck-Institut für LimnologieAbteilung ÖkophysiologiePlönFederal Republic of Germany

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