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Female and male contribution to egg size in salmonids

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Abstract

Egg size contributes to other life history traits of an individual. It is traditionally considered as a maternally determined characteristic to which the male does not have any direct contribution. However, a recent finding in insects suggests that males can affect egg size also directly. In fish, the male effect could take place only during egg swelling, as the final egg size is reached after that. We studied egg size in four freshwater salmonid species (the land-locked Atlantic salmon, the brown trout, the Arctic charr and the lake trout) right after fertilisation (initial egg size) and after the swelling phase (final egg size). The results showed that the final egg size is affected not only by the initial egg size but also by both the female and the male through the process of egg swelling. This study suggests that paternal contribution may form a previously largely ignored source of variation in early life history traits in salmonid fish.

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References

  • Alderdice, D.F. (1988) Osmotic and ionic regulation in teleost eggs and larvae. In W.S. Hoar and D.J. Randall (eds) Fish Physiology, Vol. XIA. Academic Press, Inc., London, pp. 163-251.

    Google Scholar 

  • Bernardo, J. (1996a) The particular maternal effect of propagule size, especially egg size: patterns, models, quality of evidence and interpretation. Am. Zool. 36, 216-236.

    Google Scholar 

  • Bernardo, J. (1996b) Maternal effects in animal ecology. Am. Zool. 36, 83-105.

    Google Scholar 

  • Blaxter, J.H.S. (1986) Development of sense organs and behavior of teleost larvae with special reference to feeding and predator avoidance. Trans. Am. Fish. Soc. 115, 98-114.

    Google Scholar 

  • Bolin, R.L. (1930) Embryonic development of the labrid fish, Oxyjulis californicus Günther. Copeia 1930, 122-128.

    Google Scholar 

  • Chambers, R.C. (1997) Environmental influences on egg and propagule sizes in marine fishes. In R.C. Chambers and E.A. Trippel, (eds) Early Life History and Recruitment in Fish Populations. Chapman and Hall, London, pp. 63-102.

    Google Scholar 

  • Chambers, R.C. and Leggett, W.C. (1996) Maternal influences on variation in egg sizes in temperate marine fishes. Am. Zool. 36, 180-196.

    Google Scholar 

  • Chapman, D.W. (1988) Critical review of variables used to define effects of fines in redds of large salmonids. Trans. Am. Fish. Soc. 117, 1-21.

    Google Scholar 

  • Crill, W.D., Hucy, R.B. and Gilchrist, G.W. (1996) Within-and between-generation effects of temperature on the morphology and physiology of Drosophila melanogaster. Evolution 50, 1205-1218.

    Google Scholar 

  • Daan, S., Dijkstra, C. and Tinbergen, J. (1990) Family planning in the kestrel (Falco tinnunculus) -- the ultimate control of covariation of laying date and clutch size. Behaviour 114, 83-116.

    Google Scholar 

  • Einum, S. and Fleming, I.A. (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.

    Google Scholar 

  • Fox, C.W. and Mousseau, T.A. (1998) Maternal effects as adaptations for trans-generational phenotypic plasticity in insects. In T.A. Mousseau and C.W. Fox (eds) Maternal Effects as Adaptations. Oxford University Press, New York, pp. 159-177.

    Google Scholar 

  • Groot, E.P. and Alderdice, D.F. (1985) Fine structure of the external egg membrane of five species of Pacific salmon and steelhead trout. Can. J. Zool. 63, 552-566.

    Google Scholar 

  • Gwynne, D.T. (1984) Courtship feeding increases female reproductive success in bushcrickets. Nature 307, 361-363.

    Google Scholar 

  • Heath, D.D. and Blouw, D.M. (1998) Are maternal effects in fish adaptive or merely physiological side effects? In T.A. Mousseau and C.W. Fox (eds) Maternal Effects as Adaptations. Oxford University Press, New York, pp. 178-201.

    Google Scholar 

  • Hutchings, J.A. (1991) Fitness consequences of variation in egg size and food abundance in brook trout Salvelinus fontinalis. Evolution 45, 1162-1168.

    Google Scholar 

  • Kamler, E. (1992) Early Life History of Fish: an Energetics Approach. Chapman and Hall, London.

    Google Scholar 

  • Kaplan, R.H. (1980) The implications of ovum size variability for offspring fitness and clutch size within several populations of salamanders (Ambystoma). Evolution 34, 51-64.

    Google Scholar 

  • Kaplan, R.H. (1998) Maternal effects, developmental plasticity, and life history evolution: an amphibian model. In T.A. Mousseau and C.W. Fox (eds) Maternal Effects as Adaptations, Oxford University Press, New York, pp. 244-260.

    Google Scholar 

  • Kjesbu, O.S., Solemdal, P., Bratland, P. and Fonn, M. (1996) Variation in annual egg production in individual captive Atlantic cod (Gadus morhua). Can. J. Fish. Aquat. Sci. 53, 610-620.

    Google Scholar 

  • Laale, H.W. (1980) The perivitelline space and egg envelopes of bony fishes: a review. Copeia 1980, 210-226.

    Google Scholar 

  • Lahnsteiner, F., Weismann, T. and Patzner, R.A. (1999) Physiological and biochemical parameters for egg quality determination in lake trout, Salmo trutta lacustris. Fish Phys. Biochem. 20, 375-388.

    Google Scholar 

  • Li, X., Jenssen, E. and Fyhn, H.J. (1989) Effects of salinity on egg swelling in Atlantic salmon (Salmo salar). Aquaculture 76, 317-334.

    Google Scholar 

  • Lønning, S. and Davenport, J. (1980) The swelling egg of the rough dab, Hippoglossoides plates-soides limandoides (Bloch). J. Fish Biol. 17, 359-378.

    Google Scholar 

  • Miller, T.J., Crowder, L.B., Rice, J.A. and Marschall, E.A. (1988) Larval size and recruitment mechanisms in fishes: toward a conceptual framework. Can. J. Fish. Aquat. Sci. 45, 1657-1670.

    Google Scholar 

  • Mousseau, T.A. and Fox, C.W. (1998) The adaptive significance of maternal effects. Trends Ecol. Evol. 13, 403-407.

    Google Scholar 

  • Reznick, D. (1991) Maternal effects in fish life histories. In E. Dudley (ed.) Evolutionary Biology. Discorides Press, Portland, Oregon, pp. 780-793.

    Google Scholar 

  • Rombough, P.J. (1988) Respiratory gas exchange, aerobic metabolism, and effects of hypoxia during early life. In W.S. Hoar and D.J. Randall (eds) Fish Physiology, Vol. XIA. Academic Press, Inc., London, pp. 59-161.

    Google Scholar 

  • Sakaluk, S.K. (1986) Sperm competition and the evolution of nuptial feeding behavior in the cricket, Gryllodes supplicans (Walker). Evolution 40, 584-593.

    Google Scholar 

  • Sokal, R.R. and Rohlf, F.J. (1995) Biometry: the Principles and Practice of Statistics in Biological Research. 3rd edn. W.H. Freeman and Company, New York.

    Google Scholar 

  • Tukey, J.W. (1949) One degree of freedom for non-additivity. Biometrics 5, 232-242.

    Google Scholar 

  • van den Berghe, E.P. and Gross, M.R. (1989) Natural selection resulting from female breeding competition in a Pacific salmon (coho: Oncorhynchus kisutch). Evolution 43, 125-140.

    Google Scholar 

  • Weigensberg, I., Carrière, Y. and Roff, D.A. (1998) Effects of male genetic contribution and paternal investment to egg and hatchling size in the cricket, Gryllus firmus. J. Evol. Biol. 11, 135-146.

    Google Scholar 

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Pakkasmaa, S., Peuhkuri, N., Laurila, A. et al. Female and male contribution to egg size in salmonids. Evolutionary Ecology 15, 143–153 (2001). https://doi.org/10.1023/A:1013873810905

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