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Predator avoidance behaviour of Baltic littoral mysids Neomysis integer and Praunus flexuosus

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Abstract

The predator avoidance behaviours of two littoral mysid species, Neomysis integer (Leach) and Praunus flexuosus (Müller), were studied experimentally. In ingestion experiments, mysids responded to a combination of chemical and visual signals of perch (Perca fluviatilis), but not to each stimulus alone. In the presence of the combined visual and chemical predator signal the swimming activity and choice of habitat (open vs. artificial vegetation, the Charophyte Chara tomentosa or the brown alga Fucus vesiculosus) were also influenced. The two mysid species behaved differently when perceiving predation risk: N. integer reduced swimming activity, whereas P. flexuosus increased their use of the vegetation. The different antipredator strategies of the two mysid species reflect their different lifestyles, N. integer being a swarm-forming species and P. flexuosus living in association with aquatic macrophyte vegetation.

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References

  • Aneer G (1980) Estimates of feeding pressure on pelagic and benthic organisms by Baltic herring (Clupea harengus v. membras L.). Ophelia Suppl 1:265–275

    Google Scholar 

  • Arndt EA, Jansen W (1986) Neomysis integer (Leach) in the chain of boddens south of Darss/Zingst (western Baltic)—ecophysiology and population dynamics. Ophelia Suppl 4:1–15

    Google Scholar 

  • Brönmark C, Hansson L-A (2000) Chemical communication in aquatic systems: an introduction. Oikos 88:103–109

    Google Scholar 

  • Burks RL, Jeppesen E, Lodge DM (2001) Littoral zone structures as Daphnia refugia against fish predators. Limnol Oceanogr 46:230–237

    Google Scholar 

  • Coull BC, Wells JBJ (1983) Refuges from fish predation: experiments with phytal meiofauna from the New Zealand rocky intertidal. Ecology 64:1599–1609

    Google Scholar 

  • Diehl S (1988) Foraging efficiency of three freshwater fishes: effects of structural complexity and light. Oikos 53:207–214

    Google Scholar 

  • Ejdung G (1998) Behavioural responses to chemical cues of predation risk in a three-trophic-level Baltic Sea food chain. Mar Ecol Prog Ser 165:137–144

    Google Scholar 

  • Flynn AJ, Ritz DA (1999) Effect of habitat complexity and predatory style on the capture success of fish feeding on aggregated prey. J Mar Biol Assoc UK 79:487–494

    Article  Google Scholar 

  • Fulton RS III (1982) Predatory feeding of two marine mysids. Mar Biol 72:183–191

    Google Scholar 

  • Gorokhova E (1999) Mysid growth, stable isotope fractionation, and energetics: implications for food web studies. PhD thesis, Stockholm University, Stockholm, pp 1–29

  • Gotceitas V, Colgan P (1987) Selection between densities of artificial vegetation by young bluegills avoiding predation. Trans Am Fish Soc 116:40–49

    Google Scholar 

  • Hamrén U, Hansson S (1999) A mysid shrimp (Mysis mixta) is able to detect the odour of its predator (Clupea harengus). Ophelia 51:187–191

    Google Scholar 

  • Jeppesen E, Lauridsen TL, Kairesalo T, Perrow MR (1997) Impact of submerged macrophytes on fish–zooplankton interactions in lakes. Ecol Stud 131:91–114

    Google Scholar 

  • Johansson KUI, Hallberg E (1992) Male-specific structures in the olfactory system of mysids (Mysidacea, Crustacea). Cell Tissue Res 268:359–368

    Google Scholar 

  • Kotta I, Kotta J (1999) Distribution and migration of mysids in the Gulf of Riga (northern Baltic). Proc Estonian Acad Sci Biol Ecol 48:284–295

    Google Scholar 

  • Lappalainen A, Rask M, Koponen H, Vesala S (2001) Relative abundance, diet and growth of perch (Perca fluviatilis) and roach (Rutilus rutilus) at Tvärminne, northern Baltic Sea, in 1975 and 1997: responses to eutrophication? Boreal Environ Res 6:107–118

    Google Scholar 

  • Larsson P, Dodson S (1993) Invited review. Chemical communication in planktonic animals. Arch Hydrobiol 129:129–155

    CAS  Google Scholar 

  • Lindström M (2000) Eye function of Mysidacea (Crustacea) in the northern Baltic Sea. J Exp Mar Biol Ecol 146:85–101

    Article  Google Scholar 

  • Loose CJ, von Elert E, Dawidowicz P (1993) Chemically-induced diel vertical migration in Daphnia: a new bioassay for kairomones exuded by fish. Arch Hydrobiol 126:329–337

    Google Scholar 

  • Magurran AE (1990) The adaptive significance of schooling as an anti-predator defence in fish. Ann Zool Fenn 27:51–66

    Google Scholar 

  • Mauchline J (1971) Seasonal occurrence of mysids (Crustacea) and evidence of social behaviour. J Mar Biol Assoc UK 51:809–825

    Google Scholar 

  • Mauchline J (1980) The biology of mysids and euphasiids. Adv Mar Biol 18:1–369

    Google Scholar 

  • Milinski M, Heller R (1978) Influence of a predator on the optimal foraging behaviour of sticklebacks (Gasterosteus aculeatus L.). Nature 275:642–644

    Google Scholar 

  • O'Brien DP, Ritz DA (1988) Escape responses of gregarious mysids (Crustacea: Mysidacea): towards a general classification of escape responses in aggregated crustaceans. J Exp Mar Biol Ecol 116:257–272

    Google Scholar 

  • Ohman MD (1988) Behavioral responses of zooplankton to predation. Bull Mar Sci 43:530–550

    Google Scholar 

  • Pijanowska J, Kowalczewski A (1997) Predators can induce swarming behaviour and locomotory responses in Daphnia. Freshw Biol 37:649–656

    Google Scholar 

  • Rooker JR, Holt GJ, Holt SA (1998) Vulnerability of newly settled red drum (Sciaenops ocellatus) to predatory fish: is early-life survival enhanced by seagrass meadows? Mar Biol 131:145–151

    Google Scholar 

  • Ryer CH (1988) Pipefish foraging: effects of fish size, prey size and altered habitat complexity. Mar Ecol Prog Ser 48:37–45

    Google Scholar 

  • Savino JF, Stein RA (1982) Predator–prey interaction between largemouth bass and bluegills as influenced by simulated, submersed vegetation. Trans Am Fish Soc 111:255–266

    Google Scholar 

  • Savino JF, Stein RA (1989) Behavioural interactions between fish predators and their prey: effects of plant density. Anim Behav 37:311–321

    Google Scholar 

  • Stansfield JH, Perrow MR, Tench LD, Jowitt AJD, Taylor AAL (1997) Submerged macrophytes as refuges for grazing Cladocera against fish predation: observations on seasonal changes in relation to macrophyte cover and predation pressure. Hydrobiologia 342/343:229–240

    Google Scholar 

  • Stein RA, Magnuson J (1976) Behavioral response of crayfish to a fish predator. Ecology 57:751–761

    Google Scholar 

  • Stirling G (1995) Daphnia behaviour as a bioassay of fish presence or predation. Funct Ecol 9:778–784

    Google Scholar 

  • Stoner AW (1982) The influence of benthic macrophytes on the foraging behaviour of pinfish, Lagodon rhomboides (Linnaeus). J Exp Mar Biol Ecol 58:271–284

    Google Scholar 

  • van Duren LA, Videler JJ (1996) The trade-off between feeding, mate seeking and predator avoidance in copepods: behavioural responses to chemical cues. J Plankton Res 18:805–818

    Google Scholar 

  • Viherluoto M, Viitasalo M (2001) Effect of light on the feeding rates of pelagic and littoral mysid shrimps: a trade-off between feeding success and predation avoidance. J Exp Mar Biol Ecol 261:237–244

    Article  PubMed  Google Scholar 

  • Viherluoto M, Kuosa H, Flinkman J, Viitasalo M (2000) Food utilisation of pelagic mysids, Mysis mixta and M. relicta, during their growing season in the northern Baltic Sea. Mar Biol 136:553–559

    Article  Google Scholar 

  • Viitasalo M, Rautio M (1998) Zooplanktivory by Praunus flexuosus (Crustacea: Mysidacea): functional responses and prey selection in relation to prey escape responses. Mar Ecol Prog Ser 174:77–87

    Google Scholar 

  • Visser AW (2001) Hydromechanical signals in the plankton. Mar Ecol Prog Ser 222:1–24

    Google Scholar 

  • Winfield IJ (1986) The influence of simulated aquatic macrophytes on the zooplankton consumption rate of juvenile roach, Rutilus rutilus, rudd, Scardinius eryhtrophthalmus, and perch, Perca fluviatilis. J Fish Biol 29[Suppl A]:37–48

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Acknowledgements

We thank R. Munsterhjelm for his help in the determination of macrophytes, and T. Hakala, A. Hirvonen, S. Londesborough and T. Meriläinen for their help in the collection of macrophytes. The Tvärminne Zoological Station, University of Helsinki, provided the field and laboratory facilities. This study was financed by the Walter and Andrée de Nottbeck Foundation and the Academy of Finland. The experiments comply with the current laws of Finland.

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Correspondence to E. Lindén.

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Communicated by L. Hagerman, Helsingør

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Lindén, E., Lehtiniemi, M. & Viitasalo, M. Predator avoidance behaviour of Baltic littoral mysids Neomysis integer and Praunus flexuosus . Marine Biology 143, 845–850 (2003). https://doi.org/10.1007/s00227-003-1149-x

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  • DOI: https://doi.org/10.1007/s00227-003-1149-x

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