Skip to main content
Log in

The origin and development of individual size variation in early pelagic stages of fish

  • Population Ecology
  • Published:
Oecologia Aims and scope Submit manuscript

Abstract

Size variation among individuals born at the same time in a common environment (within cohorts) is a common phenomenon in natural populations. Still, the mechanisms behind the development of such variation and its consequences for population processes are far from clear. We experimentally investigated the development of early within-cohort size variation in larval perch (Perca fluviatilis). Specifically we tested the influence of initial variation, resulting from variation in egg strand size, and intraspecific density for the development of size variation. Variation in egg strand size translated into variation in initial larval size and time of hatching, which, in turn, had effects on growth and development. Perch from the smallest egg strands performed on average equally well independent of density, whereas larvae originating from larger egg strands performed less well under high densities. We related this difference in density dependence to size asymmetries in competitive abilities leading to higher growth rates of groups consisting of initially small individuals under high resource limitation. In contrast, within a single group of larvae, smaller individuals grew substantially slower under high densities whereas large individuals performed equally well independent of density. As a result, size variation among individuals within groups (i.e. originating from the same clutch) increased under high densities. This result may be explained by social interactions or differential timing of diet shifts and a depressed resource base for the initially smaller individuals. It is concluded that to fully appreciate the effects of density-dependent processes on individual size variation and size-dependent growth, consumer feedbacks on resources need to be considered.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Bagenal TB, Braum E (1978) Eggs and early life history. In: Bagenal TB (eds) Methods for assessment of fish production in fresh waters, 3rd edn. Blackwell, Oxford, pp 165–201

    Google Scholar 

  • Bernardo J (1996) Maternal effects in animal ecology. Am Zool 36:83–105

    Google Scholar 

  • Brabrand Å (1995) Intra-cohort cannibalism among larval stages of perch (Perca Fluviatilis). Ecol Freshwater Fish 4:70–76

    Article  Google Scholar 

  • Botrell HH, Duncan A, Gliwicz ZM, Grygierik E, Larsson P, Weglenska T (1976) A rewiew of some problems in zooplankton production studies. Norw J Zool 24:419–456

    Google Scholar 

  • Byström P, Garcia-Berthou E (1999) Density-dependent growth and size specific competitive interactions in young fish. Oikos 86:217–232

    Article  Google Scholar 

  • Byström P, Persson L, Wahlström E (1998) Competing predators and prey: juvenile bottlenecks in whole-lake experiments. Ecology 79:2153–2167

    Google Scholar 

  • Byström P, Persson L, Wahlström E, Westman E (2003) Size- and density-dependent habitat use in predators: consequences for habitat shifts in young fish. J Anim Ecol 72:156–168

    Article  Google Scholar 

  • Collazo A (1996) Evolutionary correlations between early development and life history in plethodontid salamanders and teleost fishes. Am Zool 36:116–131

    Google Scholar 

  • De Roos AM, Persson L (2001) Physiologically structured models—from versatile technique to ecological theory. Oikos 94:51–71

    Article  Google Scholar 

  • De Roos AM, Persson L, McCauley E (2003) The influence of size-dependent life-history traits on the structure and dynamics of populations and communities. Ecol Lett 6:473–487

    Article  Google Scholar 

  • DeAngelis DL, Huston MA (1987) Effects of growth-rates in models of size distribution formation in plants and animals. Ecol Model 36:119–137

    Article  Google Scholar 

  • DeAngelis DL, Rose KA, Crowder LB, Marschall EA, Lika D (1993a) Fish cohort dynamics—application of complementary modeling approaches. Am Nat 142:604–622

    Article  Google Scholar 

  • DeAngelis DL, Shuter BJ, Ridgway MS, Scheffer M (1993b) Modeling growth and survival in an age-0 fish cohort. Trans Am Fish Soc 122:927–941

    Article  Google Scholar 

  • Dubois JP, Gillet C, Bonnet S, ChevalierWeber Y (1996) Correlation between the size of mature female perch (Perca fluviatilis L) and the width of their egg strands in Lake Geneva. Ann Zool Fenn 33:417–420

    Google Scholar 

  • Ebenman B (1988) Dynamics of age- and size-structured populations; intraspecific competition. In: Ebenman B, Persson L (eds) Size-structured populations: ecology and evolution. Springer, Berlin Heidelberg New York, pp 127–139

    Google Scholar 

  • Einum S (2003) Atlantic salmon growth in strongly food-limited environments: effects of egg size and paternal phenotype? Environ Biol Fish 67:263–268

    Article  Google Scholar 

  • Einum S, Fleming IA (1999) Maternal effects of egg size in brown trout (Salmo trutta): norms of reaction to environmental quality. Proc R Soc Lond B 266:2095–2100

    Article  Google Scholar 

  • Einum S, Fleming IA (2000) Highly fecund mothers sacrifice offspring survival to maximize fitness. Nature 405:565–567

    Article  PubMed  CAS  Google Scholar 

  • Fraser DF, Gilliam JF, Daley MJ, Le AN, Skalski GT (2001) Explaining leptokurtic movement distributions: intrapopulation variation in boldness and exploration. Am Nat 158:124–135

    Article  PubMed  CAS  Google Scholar 

  • Fujiwara M, Kendall BE, Nisbet RM (2004) Growth autocorrelation and animal size variation. Ecol Lett 7:106–113

    Article  Google Scholar 

  • Gillet C, Dubois JP, Bonnet S (1995) Influence of temperature and size of females on the timing of spawning of Perch, Perca fluviatilis, in Lake Geneva from 1984 to 1993. Environ Biol Fish 42:355–363

    Article  Google Scholar 

  • Harper JL (1977) The population biology of plants. Academic Press, London

    Google Scholar 

  • Heath DD, Fox CW, Heath JW (1999) Maternal effects on offspring size: variation through early development of chinook salmon. Evolution 53:1605–1611

    Article  Google Scholar 

  • Heyer CJ, Miller TJ, Binkowski FP, Caldarone EM, Rice JA (2001) Maternal effects as a recruitment mechanism in Lake Michigan yellow perch (Perca flavescens). Can J Fish Aquat Sci 58:1477–1487

    Article  Google Scholar 

  • Huston MA, DeAngelis DL (1987) Size bimodality in monospecific populations—a critical-review of potential mechanisms. Am Nat 129:678–707

    Article  Google Scholar 

  • Jacobs J (1974) Quantitative measurements of food selection: a modification of the forage ratio and Ivlev’s electivity index. Oecologia 14:413–417

    Google Scholar 

  • Johansson L, Persson L (1986) The fish community of temperate, eutrophic lakes. In: Riemann B, Søndergaard M (eds) Carbon dynamics of eutrophic, temperate lakes: the structure and functions of the pelagic environment, Elsevier, Amsterdam, pp 237–266

    Google Scholar 

  • Johnson JM, Post DM (1996) Morphological constraints on intracohort cannibalism in age-0 largemouth bass. Trans Am Fish Soc 125:809–812

    Article  Google Scholar 

  • Johnston TA (1997) Within-population variability in egg characteristics of walleye (Stizostedion vitreum) and white sucker (Catostomus commersoni). Can J Fish Aquat Sci 54:1006–1014

    Article  Google Scholar 

  • Johnston TA, Leggett WC (2002) Maternal and environmental gradients in the egg size of an iteroparous fish. Ecology 83:1777–1791

    Google Scholar 

  • Kendall BE, Fow GA (2002) Variation among individuals and reduced demographic stochasticity. Conserv Biol 16:109–116

    Article  Google Scholar 

  • Latto J (1992) The differentiation of animal body weights. Funct Ecol 6:386–395

    Article  Google Scholar 

  • Lekve K, Ottersen G, Stenseth NC, Gjosaeter J (2002) Length dynamics in juvenile coastal Skagerrak cod: effects of biotic and abiotic processes. Ecology 83:1676–1688

    Google Scholar 

  • Ludsin SA, DeVries DR (1997) First-year recruitment of largemouth bass: the interdependency of early life stages. Ecol Appl 7:1024–1038

    Google Scholar 

  • Miller TJ, Crowder LB, Rice JA, Marschall EA (1988) Larval size and recruitment mechanisms in fishes—toward a conceptual-framework. Can J Fish Aquat Sci 45:1657–1670

    Article  Google Scholar 

  • Nathanailides C, Tsoumani M, Papazogloy A, Paschos I (2002) Hatching time and post-hatch growth in Russian sturgeon Acipenser gueldenstaedtii. J Appl Ichtyol 18:651–654

    Article  Google Scholar 

  • Ozen O, Noble RL (2005) Assessing age-0 year-class strength of fast-growing largemouth bass in a tropical reservoir. N Am Fish Manage 25:163–170

    Article  Google Scholar 

  • Peacor SD, Pfister CA (2006) Experimental and model analyses of the effects of competition on individual size variation in wood frog (Rana sylvatica) tadpoles. J Anim Ecol 75:990–999

    Article  PubMed  Google Scholar 

  • Persson A, Brönmark C (2002) Foraging capacity and resource synchronization in an ontogenetic diet switcher, pikeperch (Stizostedion lucioperca). Ecology 83:3014–3022

    Article  Google Scholar 

  • Persson L (1988) Asymmetries in competitive and predatory interactions in fish populations. In: Ebenman B, Persson L (eds) Size-structured populations: ecology and evolution. Springer, Heidelberg, pp 203–218

    Google Scholar 

  • Persson L, Andersson J, Wahlström E, Eklöv P (1996) Size-specific interactions in whole-lake systems—predator gape limitation and prey growth rate and mortality. Ecology 77:900–911

    Article  Google Scholar 

  • Persson L, Byström P, Wahlström E, Nijlunsing A, Rosema S (2000) Resource limitation during early ontogeny: constraints induced by growth capacity in larval and juvenile fish. Oecologia 122:459–469

    Article  Google Scholar 

  • Persson L, Leonardsson K, de Roos AM, Gyllenberg M, Christensen B (1998) Ontogenetic scaling of foraging rates and the dynamics of a size-structured consumer-resource model. Theor Popul Biol 54:270–293

    Article  PubMed  CAS  Google Scholar 

  • Pfister CA (2003) Some consequences of size variability in juvenile prickly sculpin, Cottus asper. Environ Biol Fish 66:383–390

    Article  Google Scholar 

  • Pfister CA, Peacor SD (2003) Variable performance of individuals: the role of population density and endogenously formed landscape heterogeneity. J Anim Ecol 72:725–735

    Article  Google Scholar 

  • Pfister CA, Stevens FR (2002) The genesis of size variability in plants and animals. Ecology 83:59–72

    Google Scholar 

  • Pfister CA, Stevens FR (2003) Individual variation and environmental stochasticity: implications for matrix model predictions. Ecology 84:496–510

    Article  Google Scholar 

  • Post DM (2003) Individual variation in the timing of ontogenetic niche shifts in largemouth bass. Ecology 84:1298–1310

    Article  Google Scholar 

  • Post DM, Kitchell JF, Hodgson JR (1998) Interactions among adult demography, spawning date, growth rate, predation, overwinter mortality, and the recruitment of largemouth bass in a northern lake. Can J Fish Aquat Sci 55:2588–2600

    Article  Google Scholar 

  • Post JR, Evans DO (1989) Size-dependent overwinter mortality of young-of-the-year perch (Perca flavescens): laboratory, in situ enclosure, and field experiments. Can J Fish Aquat Sci 46:1958–1968

    Article  Google Scholar 

  • Post JR, McQueen DJ (1988) Ontogenetic changes in the distribution of larval and juvenile yellow perch (Perca flavescens): a response to prey of predators? Can J Fish Aquat Sci 45:1820–1826

    Google Scholar 

  • Reznick D (1991) Maternal effects in fish histories. In: Dudley EC (eds) The unity of evolutionary biology, vol 2. Dioscorides, Portland, Oreg., pp 780–795

  • Roff DA (1992) The evolution of life histories, theory and analysis. Chapman and Hall, New York

    Google Scholar 

  • Rubenstein DI (1981) Individual variation and competitoon in the everglades pygmy sunfish. J Anim Ecol 50:337–350

    Article  Google Scholar 

  • Schmitt J, Ehrhardt DW, Cheo M (1986) Light-dependent dominance and suppression in experimental radish populations. Ecology 67:1502–1507

    Article  Google Scholar 

  • Sebens KP (1987) The ecology of indeterminate growth in animals. Annu Rev Ecol Syst 18:371–407

    Article  Google Scholar 

  • Treasurer JW (1988) The distribution and growth of lacustrine 0+ Perch, Perca fluviatilis. Environ Biol Fish 21:37–44

    Google Scholar 

  • Uchmanski J (1985) Differentiation and frequency distributions of body weights in plants and animals. Phil Trans R Soc Lond B 310:1–75

    Article  CAS  Google Scholar 

  • Vadas RL, Smith BD, Beal B, Dowling T (2002) Sympatric growth morphs and size bimodality in the green sea urchin (Strongylocentrotus droebachiensis). Ecol Monogr 72:113–132

    Article  Google Scholar 

  • Van Densen WLT, Ligtvoet W, Roozen RWM (1996) Intra-cohort variation in the individual size of juvenile pikeperch, Stizostedion lucioperca, and perch, Perca fluviatilis, in relation to the size spectrum of their food items. Ann Zool Fenn 33:495–506

    Google Scholar 

  • Van de Wolfshaar KE (2006) Population persistence in the face of size-dependent predation and competition interactions. PhD thesis. University of Amsterdam

  • Wang N, Eckmann R (1994) Effects of temperature and food density on egg development, larval survival and growth of perch (Perca fluviatilis L). Aquaculture 122:323–333

    Article  Google Scholar 

  • Weiner J (1985) Size hierarchies in experimental populations of annual plants. Ecology 66:743–752

    Article  Google Scholar 

  • Werner EE (1988) Size, scaling and the evolution of life. In: Ebenman B, Persson L (eds) Size-structured populations: ecology and evolution. Springer, Berlin Heidelberg New York, pp 60–81

    Google Scholar 

  • Werner EE, Gilliam JF (1984) The ontogenetic niche and species interactions in size-structured populations. Annu Rev Ecol Syst 15:393–425

    Article  Google Scholar 

  • Ziemba RE, Collins JP (1999) Development of size structure in tiger salamanders: the role of intraspecific interference. Oecologia 120:524–552

    Article  Google Scholar 

  • Ziemba RE, Myers MT, Collins JP (2000) Foraging under the risk of cannibalism leads to divergence in body size among tiger salamander larvae. Oecologia 124:225–231

    Article  Google Scholar 

Download references

Acknowledgements

We thank Mårten Söderquist and Christian Tideman for field and laboratory assistance. This study was supported by grants from the Swedish Council for Forestry and Agricultural Sciences to L. Persson. The experiment in this study complies with current laws of Sweden and was approved by the Ethnical Committee at Umeå University.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Magnus Huss.

Additional information

Communicated by Anssi Laurila.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Huss, M., Persson, L. & Byström, P. The origin and development of individual size variation in early pelagic stages of fish. Oecologia 153, 57–67 (2007). https://doi.org/10.1007/s00442-007-0719-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00442-007-0719-x

Keywords

Navigation