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Genetic variation and fitness in salmonids

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Abstract

Over the last quarter century, many studieshave attempted to clarify the relationshipbetween genetic variability and fitness, butfew of these have involved salmonid fishes. Examination of studies of salmonids revealsthat such a relationship varies both among andwithin species. A correlation between geneticvariability and fitness can be affected bygenetic background, environment, and age, andit also depends upon the genetic markers andphenotypes evaluated. The relationshipsbetween molecular genetic variation,quantitative genetic variation, and phenotypicvariation may be more relevant to conservationissues than those between genetic variation andaverage fitness or performance. Consequently,future work in salmonids should include moreintensive investigation of the correspondenceof molecular genetic variation within and amongpopulations to quantitative genetic andphenotypic variation for traits affectingfitness. In the absence of a more completeunderstanding of the relationship betweengenetic variation and fitness, maintenance ofgenetic and phenotypic variation within andamong conspecific populations should beconsidered a primary goal of conservingsalmonid fishes.

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References

  • Allendorf FW, Leary RF (1986) Heterozygosity and fitness in natural populations of animals. In: Conservation Biology: the Science of Scarcity and Diversity (ed. Soulé ME), pp. 57–76. Sinauer Associates, Inc. Publishers, Sunderland, MA.

    Google Scholar 

  • Allendorf FW, Thorgaard GH (1984) Tetraploidy and the evolution of salmonid fishes. In: Evolutionary Genetics of Fishes (ed. Turner BJ), pp. 1–53. Plenum, NY.

    Google Scholar 

  • Allendorf FW, Waples RS (1996) Conservation and genetics of salmonid fishes. In: Conservation Genetics: Case Histories from Nature (eds. Avise JC, Hamrick JL), pp. 238–501. Chapman & Hall, NY.

    Google Scholar 

  • Allison DB, and Heo, M (1998) Meta-analysis of linkage data under worst-case conditions: a demonstration using the human OB region. Genetics, 148, 859–865.

    Google Scholar 

  • Armbruster P, Bradshaw WE, Holzapfel CM (1997) Evolution of the genetic architecture underlying fitness in the pitcher-plant mosquito, Wyeomyia smithii. Evolution, 51, 451–458.

    Google Scholar 

  • Avise JC (1994) Molecular Markers, Natural History and Evolution. Chapman & Hall, NY, 511 pp.

    Google Scholar 

  • Avise JC, Hamrick JL (1996) Conservation Genetics: Case Histories from Nature. Chapman & Hall, NY, 512 pp.

    Google Scholar 

  • Banks MA, Blouin MS, Baldwin BA, Rashbrook VK (1999) Isolation and inheritance of novel microsatellites in chinook salmon (Oncorhynchus tshawytscha). Journal of Heredity, 90, 281–288.

    Google Scholar 

  • Barton NH, Turelli M (1989) Evolutionary quantitative genetics: how little do we know? Annual Review of Genetics, 23, 337–370.

    Google Scholar 

  • Beacham TD (1990) A genetic analysis of meristic and morphometric variation in chum salmon (Oncorhynchus keta) at three different temperatures. Canadian Journal of Zoology, 68, 225–229.

    Google Scholar 

  • Beacham TD (1991) Developmental stability, heterozygosity, and genetic analysis of morphological variation in pink salmon (Oncorhynchus gorbuscha). Canadian Journal of Zoology, 69, 274–278.

    Google Scholar 

  • Beacham TD, Varnavskaya NV (1991) Effect of parental heterozygosity on pink salmon (Oncorhynchus gorbuscha) embryonic and alevin survival and developmental at extreme temperatures. Canadian Journal of Zoology, 69, 2485–2489.

    Google Scholar 

  • Beacham TD, Withler RE (1985a) Heterozygosity and morphological variability of pink salmon (Oncorhynchus gorbuscha) from southern British Columbia and Puget Sound. Canadian Journal of Genetics and Cytology, 27, 571–579.

    Google Scholar 

  • Beacham TD, Withler RE (1985b) Heterozygosity and morphological variability of chum salmon (Oncorhynchus keta) in southern British Columbia. Heredity, 54, 313–322.

    Google Scholar 

  • Beacham TD, Withler RE (1987) Developmental stability and heterozygosity in chum (Oncorhynchus keta) and pink (Oncorhynchus gorbuscha) salmon. Canadian Journal of Zoology, 65, 1823–1826.

    Google Scholar 

  • Bierne N, Tsitrone A, David P (2000) An inbreeding model of associative overdominance during a population bottleneck. Genetics, 155, 1981–1990.

    Google Scholar 

  • Blanchfield PJ, Jones MW (2000) Conference report: reproductive success in salmonids. Reviews in Fish Biology and Fisheries, 10, 119–121.

    Google Scholar 

  • Blanco G, Presa P, Vazquez E, Sanchez JA (1998) Allozyme heterozygosity and development in Atlantic salmon, Salmo salar. Fish Physiology and Biochemistry, 19, 163–169.

    Google Scholar 

  • Blanco G, Sanchez JA, Vazquez E, Garcia E, Rubio J (1990) Superior developmental stability of heterozygotes at enzyme loci in Salmo salar. Aquaculture, 84, 199–209.

    Google Scholar 

  • Britten HB (1996) Meta-analyses of the association between multilocus heterozygosity and fitness. Evolution, 50, 2158–2164.

    Google Scholar 

  • Busack CA, Currens KP (1995) Genetic risks and hazards in hatchery operations: fundamental concepts and issues. American Fisheries Society Symposium, 15, 71–80.

    Google Scholar 

  • Caughley G, Gunn A (1996) Conservation Biology in Theory and Practice. Blackwell Science, Cambridge, MA, 459 pp.

    Google Scholar 

  • Charlesworth D, Charlesworth B (1987) Inbreeding depression and its evolutionary consequences. Annual Review of Ecology and Systematics, 18, 237–268.

    Google Scholar 

  • Comstock RE, Robinson HF (1952) Estimation of average dominance of genes. In: Heterosis (ed. Gowen JW), pp. 494–516. Iowa State University Press, Ames, IA.

    Google Scholar 

  • Crandall KA, Bininda-Emonds ORP, Mace GM, Wayne RK (2000) Considering evolutionary processes in conservation biology. Trends in Ecology and Evolution, 15, 290–295.

    Google Scholar 

  • Crnokrak P, Roff DA (1999) Inbreeding depression in the wild. Heredity, 83, 260–270.

    Google Scholar 

  • Crozier WW (1997) Genetic heterozygosity and meristic character variance in a wild Atlantic salmon population and a hatchery strain derived from it. Aquaculture International, 5, 407–414.

    Google Scholar 

  • Danzmann RG, Ferguson MM (1988) Developmental rates of heterozygous and homozygous rainbow trout reared at three temperatures. Biochemical Genetics, 26, 53–67.

    Google Scholar 

  • Danzmann RG, Ferguson MM, Allendorf FW (1985) Does enzyme heterozygosity influence developmental rate in rainbow trout? Heredity, 56, 417–425.

    Google Scholar 

  • Danzmann RG, Ferguson MM, Allendorf FW, Knudsen KL (1986) Heterozygosity and developmental rate in a strain of rainbow trout (Salmo gairdneri). Evolution, 40, 86–93.

    Google Scholar 

  • Danzmann RG, Ferguson MM, Allendorf FW (1987) Heterozygosity and oxygen-consumption rate as predictors of growth and developmental rate in rainbow trout. Physiological Zoology, 60, 211–220.

    Google Scholar 

  • Danzmann RG, Ferguson MM, Allendorf FW (1988) Heterozygosity and components of fitness in a strain of rainbow trout. Biological Journal of the Linnaean Society, 33, 285–304.

    Google Scholar 

  • Danzmann RG, Ferguson MM, Allendorf FW (1989) Genetic variability and components of fitness in hatchery strains of rainbow trout. Journal of Fish Biology, 35 (Supplement A), 313–319.

    Google Scholar 

  • David P (1998) Heterozygosity-fitness correlations: new perspectives on old problems. Heredity, 80, 531–537.

    Google Scholar 

  • Dobzhansky T (1970) Genetics of the Evolutionary Process. Columbia University Press, New York.

    Google Scholar 

  • Dubrova YE, Salmenkova EA, Altukhov YP, Kartavtsev YF, Kalkova EV, Omel'Chenko VT (1995) Family heterozygosity and progeny body length in pink salmon Oncorhynchus gorbuscha (Walbaum). Heredity, 75, 281–289.

    Google Scholar 

  • Eanes WF (1987) Allozymes and fitness: evolution of a problem. Trends in Ecology and Evolution, 2, 44–48.

    Google Scholar 

  • Endler JA (1986) Natural Selection in theWild. Princeton University Press, Princeton, NJ, 336 pp.

    Google Scholar 

  • Falconer DS, Mackay TFC (1996) Introduction to Quantitative Genetics, 4th edn. Longman, Harlow, UK, 480 pp.

    Google Scholar 

  • Ferguson MM (1990) Enzyme heterozygosity and growth of rainbow trout reared at two rations. Biological Journal of the Linnaean Society, 40, 215–227.

    Google Scholar 

  • Ferguson MM (1992) Enzyme heterozygosity and growth in rainbow trout: genetic and physiological explanations. Heredity, 68, 115–122.

    Google Scholar 

  • Ferguson MM, Danzmann RG, Allendorf FW (1985) Developmental divergence among hatchery strains of rainbow trout (Salmo gairdneri). I. Pure strains. Canadian Journal of Genetics and Cytology, 27, 289–297.

    Google Scholar 

  • Ferguson MM, Drahushchak LR (1990) Disease resistance and enzyme heterozygosity in rainbow trout. Heredity, 64, 413–417.

    Google Scholar 

  • Ferguson MM, Knudsen KL, Danzmann RG, Allendorf FW (1988) Developmental rate and viability of rainbow trout with a null allele at a lactate dehydrogenase locus. Biochemical Genetics, 26, 177–189.

    Google Scholar 

  • Frankel OH, Soulé ME (1981) Conservation and Evolution. Cambridge University Press, Cambridge, UK, 327 pp.

    Google Scholar 

  • Frankham R (1995a) Conservation genetics. Annual Review of Genetics, 29, 305–327.

    Google Scholar 

  • Frankham R (1995b) Effective population size/adult population size ratios in wildlife: a review. Genetical Research, Cambridge, 66, 95–106.

    Google Scholar 

  • Franklin IR (1977) The distribution of the proportion of the genome which is homozygous by descent in inbred individuals. Theoretical Population Biology, 11, 60–80.

    Google Scholar 

  • Gall GAE (1987) Inbreeding. In: Population Genetics & Fisheries Management (eds. Ryman N, Utter F), pp. 47–80. University of Washington Press, Seattle, WA.

    Google Scholar 

  • Gjerde B, Schaeffer LR (1989) Body traits in rainbow trout. II. Estimates of heritabilities and of phenotypic and genetic correlations. Aquaculture, 80, 25–44.

    Google Scholar 

  • Grant WS, García-Marín JL, Utter FM (1999) Defining population boundaries for fishery management. In: Genetics in Sustainable Fisheries Management (ed. Mustafa S), pp. 27–72. Fishing News Books, Blackwell Science, Oxford, UK.

    Google Scholar 

  • Gustafsson L (1986) Lifetime reproductive success and heritability: empirical support for Fisher's fundamental theorem. American Naturalist, 128, 761–764.

    Google Scholar 

  • Hard JJ (1995a) Genetic monitoring of life-history characters in salmon supplementation: problems and opportunities. American Fisheries Society Symposium, 15, 212–225.

    Google Scholar 

  • Hard JJ (1995b) A quantitative genetic perspective on the conservation of intraspecific diversity. American Fisheries Society Symposium, 17, 304–326.

    Google Scholar 

  • Hard JJ, Winans GA, Richardson JC (1999) Phenotypic and genetic architecture of juvenile morphometry in chinook salmon. Journal of Heredity, 90, 597–606.

    Google Scholar 

  • Hard JJ, Connell L, Hershberger WK, Harrell LW (2000) Genetic variation in mortality of chinook salmon (Oncorhynchus tshawytscha) during a bloom of the marine alga Heterosigma akashiwo. Journal of Fish Biology, 56, 1387–1397.

    Google Scholar 

  • Hedrick PW, Kalinowski ST (2000) Inbreeding depression in conservation biology. Annual Review of Ecology and Systematics, 31, 139–162.

    Google Scholar 

  • Hedrick PW, Miller PS (1992) Conservation genetics: techniques and fundamentals. Ecological Applications, 2, 30–46.

    Google Scholar 

  • Hegmann JP, Dingle H (1982) Phenotypic and genotypic covariance structure in milkweed bug life history traits. In: Evolution and Genetics of Life Histories (ed. Dingle H, Hegmann JP), pp. 177–182. Springer-Verlag, New York.

    Google Scholar 

  • Kapuscinski ARD, Lannan JE (1984) Application of a conceptual genetic fitness model for managing Pacific salmon fisheries. Aquaculture, 43, 135–146.

    Google Scholar 

  • Kapuscinski ARD, Lannan JE (1986) A conceptual genetic fitness model for fisheries management. Canadian Journal of Fisheries and Aquatic Sciences, 43, 1606–1616.

    Google Scholar 

  • Kartavtsev YP (1992) Allozyme heterozygosity and morphological homeostasis in pink salmon, Oncorhynchus gorbuscha (Walbaum): evidences from family analysis. Journal of Fish Biology, 40, 17–24.

    Google Scholar 

  • Kartavtsev YP (1998) Analysis of association between allozyme variability and fitness characteristics in the fry of pink salmon (Oncorhynchus gorbuscha) in mass crosses. Russian Journal of Marine Biology, 24, 32–35.

    Google Scholar 

  • Keightley PD, Hill WG (1992) Quantitative genetic variation in body size of mice from new mutations. Genetics, 131, 693–700.

    Google Scholar 

  • Koljonen M (1986) The enzyme gene variation of ten Finnish rainbow trout strains and the relation between growth rate and mean heterozygosity. Aquaculture, 57, 253–260.

    Google Scholar 

  • Knudsen KL, Leary RF, Talluri M (1984) Reduced developmental stability of null allele heterozygotes at two lactate dehydrogenase loci in rainbow trout. Genetics, 107, pt. 2, p. s57.

    Google Scholar 

  • Krueger CC, May B (1991) Ecological and genetic effects of salmonid introductions in North America. Canadian Journal of Fisheries and Aquatic Sciences, 48 (Supplement 1), 66–77.

    Google Scholar 

  • Kruuk LEB, Clutton-Brock TH, Slate J, Pemberton JM, Brotherstone S, Guinness FE (2000) Heritability of fitness in a wild mammal population. Proceedings of the National Academy of Sciences, USA, 97, 698–703.

    Google Scholar 

  • Lande R (1976) The maintenance of genetic variability by mutation in a polygenic character with linked loci. Genetical Research, Cambridge, 26, 221–235.

    Google Scholar 

  • Lande R (1981) The minimum number of genes contributing to quantitative variation between and within populations. Genetics, 99, 541–553.

    Google Scholar 

  • Lande R, Barrowclough GF (1987) Effective population size, genetic variation, and their use in population management. In: Viable Populations for Conservation (ed. Soulé ME), pp. 87–123. Cambridge University Press, Cambridge, UK.

    Google Scholar 

  • Lande R, Arnold SJ (1983) The measurement of selection on correlated characters. Evolution, 37, 1210–1226.

    Google Scholar 

  • Lande R, Schemske DW (1985) The evolution of self-fertilization and inbreeding depression in plants. I. Genetic models. Evolution, 39, 24–40.

    Google Scholar 

  • Landweber LF, Dobson AP (eds.) (1999) Genetics and the Extinction of Species: DNA and the Conservation of Biodiversity. Princeton University Press, Princeton, NJ, 189 pp.

    Google Scholar 

  • Leary RF, Allendorf FW, Knudsen KL (1983) Developmental stability and enzyme heterozygosity in rainbow trout. Nature, London, 301, 71–72.

    Google Scholar 

  • Leary RF, Allendorf FW, Knudsen KL (1984) Superior developmental stability of heterozygotes at enzyme loci in salmonid fishes. American Naturalist, 124, 540–551.

    Google Scholar 

  • Leary RF, Allendorf FW, Knudsen KL (1985) Inheritance of meristic variation and the developmental stability in rainbow trout. Evolution, 39, 308–314.

    Google Scholar 

  • Leary RF, Allendorf FW, Knudsen KL (1987) Differences in inbreeding coefficients do not explain the association between heterozygosity at allozyme loci and developmental stability in rainbow trout. Evolution, 41, 1413–1415.

    Google Scholar 

  • Leary RF, Allendorf FW, Knudsen KL (1991) Effects of rearing density on meristics and developmental stability of rainbow trout. Copeia, 1, 44–49.

    Google Scholar 

  • Leary RF, Allendorf FW, Knudsen KL (1992) Genetic, environmental, and developmental causes of meristic variation in rainbow trout. Acta Zoologica Fennica, 191, 79–95.

    Google Scholar 

  • Leung B, Forbes MR, Houle D (2000) Fluctuating asymmetry as a bioindicator of stress: comparing efficacy of analysis involving multiple traits. American Naturalist, 155, 101–115.

    Google Scholar 

  • Liskauskas AP, Ferguson MM (1990) Enzyme heterozygosity and fecundity in a naturalized population of brook trout (Salvelinus fontinalis). Canadian Journal of Fisheries and Aquatic Sciences, 47, 2010–2015.

    Google Scholar 

  • Liskauskas AP, Ferguson MM (1991) Genetic variation and fitness: a test in a naturalized population of brook trout (Salvelinus fontinalis). Canadian Journal of Fisheries and Aquatic Sciences, 48, 2152–2162.

    Google Scholar 

  • Loeschcke V, Tomiuk J, Jain SK (1994) Introductory remarks: genetics and conservation biology. In: Conservation Genetics (eds. Loeschcke V, Tomiuk J, Jain SK), pp. 3–8. Birkhäuser Verlag, Basel, Switzerland.

    Google Scholar 

  • Lynch M(1988) Design and analysis of experiments on random drift and inbreeding depression. Genetics, 120, 791–807.

    Google Scholar 

  • Lynch M (1996) A quantitative-genetic perspective on conservation issues. In: Conservation Genetics: Case Histories from Nature (eds. Avise JC, Hamrick JL), pp. 471–501. Chapman & Hall, NY.

    Google Scholar 

  • Lynch M, Walsh B (1998) Genetics and Analysis of Quantitative Traits. Sinauer Associates, Inc., Sunderland, MA, 980 pp.

    Google Scholar 

  • Lynch M, Pfrender M, Spitze K, Lehman N, Hicks J, Allen D, Latta L, Ottene M, Bogue F, Colbourne J (1999) The quantitative and molecular genetic architecture of a subdivided species. Evolution, 53, 100–110.

    Google Scholar 

  • Marshall TC, Slate J, Kruuk L, Pemberton JM (1998) Statistical confidence for likelihood-based paternity inference in natural populations. Molecular Ecology, 7, 639–655.

    Google Scholar 

  • Mitton JB (1993a) Enzyme heterozygosity, metabolism, and developmental stability. Genetica, 89, 47–65.

    Google Scholar 

  • Mitton JB (1993b) Theory and data pertinent to the relationship between heterozygosity and fitness. In: The Natural History of Inbreeding and Outbreeding: Theoretical and Empirical Perspectives (ed. Thornhill NW), pp. 17–41. The University of Chicago Press, Chicago, IL.

    Google Scholar 

  • Mitton JB (1997) Selection in Natural Populations. Oxford University Press, New York, NY, 240 pp.

    Google Scholar 

  • Moran P (2002) Current conservation genetics: building an ecological approach to the synthesis of molecular and quantitative genetic methods. Ecology of Freshwater Fish, 11, 30–55.

    Google Scholar 

  • Morgan MT, Conner JK (2001) Using genetic markers to directly estimate male selection gradients. Evolution, 55, 272–281.

    Google Scholar 

  • National Research Council (NRC) (1996) Upstream: Salmon and Society in the Pacific Northwest. National Academic Press, Washington, D.C., 452 pp.

    Google Scholar 

  • Pray LA, Schwartz JM, Goodnight CJ, Stevens L (1994) Environmental dependency of inbreeding depression: implications for conservation biology. Conservation Biology, 8, 562–568.

    Google Scholar 

  • Quinn TP, Unwin MJ, Kinnison MT (2000) Evolution of temporal isolation in the wild: genetic divergence in timing of migration and breeding by introduced chinook salmon populations. Evolution, 54, 1372–1385.

    Google Scholar 

  • Ralls K, Ballou J (1983) Extinction: lessons from zoos. In: Genetics and Conservation (eds. Schonewald-Cox CM, Chambers SM, MacBryde B, Thomas L), pp. 164–184. Benjamin/Cummings, Menlo Park, CA.

    Google Scholar 

  • Ralls K, Ballou JD, Templeton AR (1988) Estimates of lethal equivalents and the cost of inbreeding in mammals. Conservation Biology, 2, 185–193.

    Google Scholar 

  • Ritland K (1996) A marker-based method for inferences about quantitative inheritance in natural populations. Evolution, 50, 1062–1073.

    Google Scholar 

  • Ritland K (2000) Marker-inferred relatedness as a tool for detecting heritability in nature: Invited Review. Molecular Ecology, 9, 1195–1204.

    Google Scholar 

  • Rose MR (1982) Antagonistic pleiotropy, dominance, and genetic variation. Heredity, 48, 63–78.

    Google Scholar 

  • Ryman N (1970) A genetic analysis of recapture frequencies of released young of salmon (Salmo salar L.). Hereditas, 71, 237–244.

    Google Scholar 

  • Ryman N (1991) Conservation genetics considerations in fishery management. Journal of Fish Biology, 39 (Supplement A), 211–224.

    Google Scholar 

  • Ryman N, Laikre L (1991) Effects of supportive breeding on the genetically effective population size. Conservation Biology, 5, 325–329.

    Google Scholar 

  • Ryman N, Utter F, Laikre L (1995) Protection of intraspecific biodiversity of exploited fishes. Reviews in Fish Biology and Fisheries, 4, 417–446.

    Google Scholar 

  • Saccheri I, KuussaariM, KankareM, Vikman P, Fortelius W, Hanski I (1998) Inbreeding and extinction in a butterfly metapopulation. Nature, London, 392, 491–494.

    Google Scholar 

  • Service PM, Rose MR (1985) Genetic covariation among lifehistory components: the effect of novel environments. Evolution, 39, 943–945.

    Google Scholar 

  • Sheffer RJ, Hedrick PW, Velasco AL (1999) Testing for inbreeding and outbreeding depression in the endangered Gila topminnow. Animal Conservation, 2, 121–129.

    Google Scholar 

  • Slate J, Kruuk LEB, Marshall TC, Pemberton JM, Clutton-Brock TH (2000) Inbreeding depression influences lifetime breeding success in a wild population of red deer (Cervus elaphus). Proceedings of the Royal Society Biological Sciences Series B, 267, 1657–1662.

    Google Scholar 

  • Smouse PE, Meagher TR, Kobak CJ (1999) Parentage analysis in Chamaelirium luteum (L.) Gray (Liliaceae): why do some males have disproportionate reproductive contributions? Journal of Evolutionary Biology, 12, 1069–1977.

    Google Scholar 

  • Soulé M, Gilpin M, Conway W, Foose T (1986) The Millenium Ark: how long a voyage, how many staterooms, how many passengers? Zoo Biology, 5, 101–113.

    Google Scholar 

  • Soulé ME (1987) Viable Populations for Conservation. Cambridge University Press, Cambridge, UK, 189 pp.

    Google Scholar 

  • Soulé ME, Wilcox BA (eds.) (1980) Conservation Biology: An Evolutionary-Ecological Perspective. Sinauer Associates, Inc., Sunderland, MA, 395 pp.

    Google Scholar 

  • Spruell P, Pilgrim KL, Greene BA, Habicht C, Knudsen KL, Lindner KR, Olsen JB, Sage GK, Seeb JE, Allendorf FW (1999) Inheritance of nuclear DNA markers in gynogenetic haploid pink salmon. Journal of Heredity, 90, 289–296.

    Google Scholar 

  • Stoneking M, May B, Wright JE (1981) Loss of duplicate gene expression in salmonids: evidence for a null allele polymorphism at the duplicate aspartate aminotransferase loci in brook trout (Salvelinus fontinalis). Biochemical Genetics, 19, 1063–1077.

    Google Scholar 

  • Storfer A (1996) Quantitative genetics: a promising approach for the assessment of genetic variation in endangered species. Trends in Ecology and Evolution, 11, 343–348.

    Google Scholar 

  • Thelen GC, Allendorf FW (2001) Heterozygosity-fitness correlations in rainbow trout: allozyme loci or associative overdominance? Evolution, 55, 1180–1187.

    Google Scholar 

  • Utter F (2001) Patterns of subspecific anthropogenic introgression in two salmonid genera. Reviews in Fish Biology and Fisheries, 10, 435–451.

    Google Scholar 

  • Utter F, Hindar K, Ryman N (1993) Genetic effects of aquaculture on natural salmonid populations. In: Salmon Aquaculture (eds. Heen K, Monahan RL, Utter F), pp. 144–165. Fishing News Books, Oxford, UK.

    Google Scholar 

  • Van Dongen S (1999) Accuracy and power in fluctuating asymmetry studies: effects of sample size and number of within-subject repeats. Journal of Evolutionary Biology, 12, 547–550.

    Google Scholar 

  • Via S, Lande R (1985) Genotype-environment interaction and the evolution of phenotypic plasticity. Evolution, 39, 505–522.

    Google Scholar 

  • Vollestad LA, Hindar K (1997) Developmental stability and environmental stress in Salmo salar (Atlantic salmon). Heredity, 78, 215–222.

    Google Scholar 

  • Wang S, Utter FM, Hard JJ (in review) Salmonid inbreeding: a review. Reviews in Fish Biology and Fisheries.

  • Waples RS (1990a) Conservation genetics of Pacific salmon. II. Effective population size and the rate of loss of genetic variability. Journal of Heredity, 81, 267–276.

    Google Scholar 

  • Waples RS (1990b) Conservation genetics of Pacific salmon. III. Estimating effective population size. Journal of Heredity, 81, 277–289.

    Google Scholar 

  • Waples RS, Do C (1994) Genetic risk associated with supplementation of Pacific salmonids: Captive broodstock programs. Canadian Journal of Fisheries and Aquatic Sciences, 51 (Supplement 1), 310–329.

    Google Scholar 

  • Ward RD, Grewe PM (1994) Appraisal of molecular genetic techniques in fishes. Reviews in Fish Biology and Fisheries, 4, 300–325.

    Google Scholar 

  • Whitlock M (1993) Lack of correlation between heterozygosity and fitness in forked fungus beetles. Heredity, 70, 574–581.

    Google Scholar 

  • Williams GC (1966) Adaptation and Natural Selection. A Critique of Some Current Evolutionary Thought. Princeton University Press, Princeton, NJ.

    Google Scholar 

  • Wright S (1968) Evolution and the Genetics of Populations, v. I. Genetics and Biometric Foundations. University of Chicago Press, Chicago, IL, 469 pp.

    Google Scholar 

  • Zouros E (1993) Associative overdominance: evaluating the effects of inbreeding and linkage disequilibrium. Genetics, 89, 35–46.

    Google Scholar 

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Wang, S., Hard, J.J. & Utter, F. Genetic variation and fitness in salmonids. Conservation Genetics 3, 321–333 (2002). https://doi.org/10.1023/A:1019925910992

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