Abstract
Animals often prefer areas containing physical structure, and population density often increases with structural complexity, presumably because physical complexity in habitats may offer protection from predators and aggressive competitors. Consequently, increased habitat complexity often results in reduced territory size, lower aggression levels and reduced resource monopolisation by dominants. If behavioural plasticity is limited at early life stages, increased habitat complexity may reduce the relative fitness of aggressive, dominant strategies. Here we tested this hypothesis in an experiment on newly emerged brown trout (Salmo trutta) fry. We show, for the first time, that increased habitat complexity reduces the fitness (i.e. growth rate) of aggressive dominant individuals in relation to subordinates, and that this relation is reversed in simple habitats. Variation in environmental complexity may thus induce fluctuating selective pressures, maintaining behavioural variation in natural populations and allowing subordinate and dominant strategies to coexist.
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References
Basquill SP, Grant JWA (1998) An increase in habitat complexity reduces aggression and monopolization of food by zebra fish (Danio rerio). Can J Zool 76:770–772
Brännäs E (1995) First access to territorial space and exposure to strong predation pressure: a conflict in early emerging Atlantic salmon (Salmo salar) fry. Evol Ecol 9:411–420
Burger J (1974) Breeding adaptations of Franklin’s gull (Larus pipixcan) to a marsh habitat. Anim Behav 22:521–567
Calsbeek R, Sinervo B (2002) An experimental test of the ideal despotic distribution. J Anim Ecol 71:513–523
Coulston PJ, Maughan OE (1983) Effects of removal of instream debris on trout population. J Elisha Mitchell Sci Soc 99:78–85
Eason PK, Stamps JA (1992) The effect of visibility on territory size and shape. Behav Ecol 3:166-172
Elliott JM (1994) Quantitative ecology and the brown trout. Oxford University Press, Oxford
Endler JA (1995) Multiple-trait coevolution and environmental gradients in guppies. Trends Ecol Evol 10:22–29
Floater GJ (2001) Habitat complexity, spatial interference, and “minimum risk distribution”: a framework for population stability. Ecol Monogr 71:447–468
Gallup GG (1968) Mirror-image stimulation. Physiol Bull 70:782–793
Gowan C, Fausch KD (1996) Long term demographic responses of trout populations to habitat manipulations in six colorado streams. Ecol Appl 6:931–946
Harmon ME, Franklin JF, Swanson FJ, Sollins P, Gregory SV, Lattin JD, Anderson NH, Cline SP, Aumen NG, Sedell JR, Lienkamper GW, Cromack K Jr, Cummins KW (1986): Ecology of coarse woody debris in temperate ecosystems. Adv Ecol Res 15:133–302
Höjesjö J, Johnsson JI, Bohlin T (2002) Can laboratory studies on dominance predict fitness of young brown trout in the wild? Behav Ecol Sociobiol 52:102–108
Huntingford FA (1993) Development of behaviour in fish In: Pitcher TJ (ed) Behaviour of teleost fishes. Chapman & Hall, London, pp 57–83
Imre I, Grant JWA, Keeley ER (2002) The effect of visual isolation on territory size and population density of juvenile rainbow trout (Oncorhynchus mykiss). Can J Fish Aquat Sci 59:303–309
Jarman PJ (1974): The social organisation of antelope in relation to their ecology. Behaviour 48:245–267
Jensen SP, Gray SJ, Hurst JL (2003) How does habitat structure affect activity and use of space among house mice? Anim Behav 66:239–250
Jordan F, Babbitt-Kimberly J, McIvor-Carole S, Miller-Steven J (1996) Spatial ecology of the crayfish Procabarus alleni in a Florida wetland mosaic. Wetlands 16:134–142
Kalleberg H (1958) Observation in a stream tank of territoriality and competition in juvenile salmon and trout (Salmo salar L. and S.trutta). Inst Freshw Res Drott Rep 39:55–98
Keenleyside MA, Yamamoto FT (1962) Territorial behaviour in juvenile Atlantic salmon (Salmo salar). Behaviour 19:139–169
Metcalfe NB, Taylor AC, Thorpe JE (1995) Metabolic rate, social status and life history strategies in Atlantic salmon. Anim Behav 49:431-436
Ricker WE (1979) Growth rates and models In: Hoar WS, Randall DJ, Brett JR (eds) Fish physiology, vol 8. Bioenergetics and growth. Academic Press, New York, pp 677–743
Rosenzweig ML (1991) Habitat selection and population interactions: the search for mechanism. Am Nat 137 [suppl]:5–28
Savino JF, Stein RA (1982) Predator prey interactions between largemouth bass and bluegills as influenced by simulated submersed vegetation. Trans Am Fish Soc 111:255–266
Schoener TW (1987) The growth cost of terrotorial overlap in a juvenile lizard (Anolis aeneus). Behav Ecol Sociobiol 15:115–119
Stamps J (2003) Anniversary essay Behavioural processes affecting development: Tinbergen’s fourth question comes of age. Anim Behav 66:1–13
Sundbaum K, Näslund I (1998) Effects of woody debris on the growth and behaviour of brown trout in experimental stream channels. Can J Zool 76:56–61
Acknowledgements
Professor Neil Metcalfe and Dr. Tobias Uller provided valuable comments on earlier versions of the manuscript. Eva Andersson and Marina Johansson helped us with observing and feeding the fish. Johan Höjesjö was financially supported by Helge Ax:son Johnsson foundation and Vitterhetsamhället. The experiment reported here complies with the current laws in Sweden.
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Höjesjö, J., Johnsson, J. & Bohlin, T. Habitat complexity reduces the growth of aggressive and dominant brown trout (Salmo trutta) relative to subordinates. Behav Ecol Sociobiol 56, 286–289 (2004). https://doi.org/10.1007/s00265-004-0784-7
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DOI: https://doi.org/10.1007/s00265-004-0784-7