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Genetic variation and covariation during larval and juvenile growth in Mercenaria mercenaria

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Abstract

Quantitative genetic variances and covariances were estimated for shell length of the hard clam Mercenaria mercenaria (L.) at three larval stages (prodissoconch I, 2 d and 10 d post-fertilization) in 1987 and in 1988 after ca. 9 mo of growth. At each sample interval additive genetic variance was a highly significant component of the total size variation. Narrow sense heritability estimates for shell length ranged between 0.58 (±0.10) for prodissoconch I and 1.08 (±0.29) for 2-d-old larvae. There was significant and positive genetic covariance in prodissoconch I and 2-d larval shell length which resulted in a highly significant genetic correlation (r g=0.74) between these two traits. This covariance is not surprising since the prodissoconch I comprises the majority of the larval shell of a 2-d-old larvae. The genetic covariances between 2-d-old and 10-d-old larvae and between 10-d-old larvae and 9-mo-old juveniles were low and not significantly different from zero. These results indicate that there is substantial genetic variation for shell growth in M. mercenaria but this variation is not stable during development; the genetic variation in shell growth at one stage of development is not strongly related to the genetic variation in growth during other ontogenetic periods. In this study there were no evident constraints to natural selection for increased shell growth rate during development, which coupled with the high levels of genetic variation may suggest that in nature high rates of larval growth may not be normally subject to significant selective pressure.

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Literature cited

  • Bayne, B. L. (1983). Physiological ecology of marine molluscan larvae. In: Verdonk, N. H., van den Biggelaar, J. A. M., Tompa, A. S. (eds.) The Mollusca, Vol. 3. Development. Academic Press, New York, p. 299–343

    Google Scholar 

  • Becker, W. A. (1984). Manual of quantitative genetics. Academic Enterprises. Pullman, Washington

    Google Scholar 

  • Carter, J. C. (1980). Selected mineralogical data for the Bivalvia. In: Rhoads, D. C., Lutz, R. A. (eds.) Skeletal growth of aquatic organisms. Plenum Press, New York, p. 69–113

    Google Scholar 

  • Comstock, R. E., Robinson, H. F. (1952). Estimation of average dominance of genes. In: Gowen J. W. (ed.) Heterosis. Iowa State College Press, Ames, p. 494–516

    Google Scholar 

  • Coon, S. L., Fitt, W. K., Bonar, D. B. (1990). Competency and delay of metamorphosis in the Pacific oyster, Crassostrea gigas (Thunberg). Mar. Biol. 106: 379–387

    Google Scholar 

  • Davidson, E. H. (1986). Gene activity in early development. Academic Press, Orlando

    Google Scholar 

  • Eyster, L. S., Pechnik, J. A. (1987). Attachment of Mytilus edulis L. larvae on algal and byssal filaments is enhanced by water agitation. J. exp. mar. Biol. Ecol. 114: 99–110

    Google Scholar 

  • Falconer, D. S. (1952). The problem of environment and selection. Am. Nat. 86: 293–298

    Google Scholar 

  • Falconer, D. S. (1981). Introduction to quantitative genetics. Longman Press, New York

    Google Scholar 

  • Freund, R. J., Littel, R. C., Spector, P. C. (1986). SAS System for linear models. SAS Institute, Cary, North Carolina

    Google Scholar 

  • Friedman, G. M. (1959). Identification of carbonate minerals by staining methods. J. sedim. Petrol. 29: 87–97

    Google Scholar 

  • Gaffney, P. M., Scott, T. M., Koehn, R. K., Diehl, W. J. (1990). Interrelationships of heterozygosity, growth rate and heterozygote deficiencies in the coot clam, Mulinia lateralis. Genetics, Baltimore, MD. 124: 687–699

    Google Scholar 

  • Gillespie, J. H., Turelli, M. (1989). Genotype-environment interactions and the maintenance of polygenic variation. Genetics, Baltimore, MD 121: 129–138

    Google Scholar 

  • Haley, L. E. Newkirk, G. F. (1977). Selecting oysters for faster growth. Proc. Wld Maricult. Soc. 8: 557–565

    Google Scholar 

  • Highsmith, R. C., Emlet, R. B. (1986). Delayed metamorphosis: effect on growth and survival of juvenile sand dollars (Echinoidea: Clypeasteroida). Bull. mar. Sci. 39: 347–361

    Google Scholar 

  • Innes, D. J., Haley, L. E. (1977). Genetic aspects of larval growth under reduced salinity in Mytilus edulis. Biol. Bull. mar. biol. Lab., Woods Hole 153: 312–321

    Google Scholar 

  • Jablonski, D., Lutz, R. A. (1980). Molluscan larval shell morphology: ecological and paleontological applications. In: Rhoads, D. C., Lutz, R. A. (eds.) Skeletal growth of aquatic organisms. Plenum Press, New York, p. 323–377

    Google Scholar 

  • Jablonski, D., Lutz, R. A. (1983). Larval ecology of marine benthic invertebrates: paleobiological implications. Biol. Rev. 58: 21–89

    Google Scholar 

  • Koehn, R. K., Diehl, W. J., Scott, T. M. (1988). The differential contribution by individual enzymes of glycolysis and protein catabolism to the relationship between heterozygosity and growth rate in the coot clam, Mulinia lateralis. Genetics, Baltimore, MD 119: 121–130

    Google Scholar 

  • Koehn, R. K., Gaffney, P. M. (1984). Genetic heterozygosity and growth rate in Mytilus edulis Mar. Biol. 82: 1–7

    Google Scholar 

  • Kraeuter, J. N., Castagna, M., Dessel, R. van (1982). Egg size and larval survival of Mercenaria mercenaria (L.) and Argopecten irradians (Lammarck). J. exp. mar. Biol. Ecol. 56: 3–8

    Google Scholar 

  • Levin, L. A., Zhu, J., Creed, E. (1991). The genetic basis of life-history characters in a polychaete exhibiting planktotrophy and lecithothropy. Evolution, Lawrence, Kansas 45: 380–397

    Google Scholar 

  • Losee, E. (1978). Influence of heredity on larval and spat growth in Crassostrea virginica. Proc. Wld Maricult. Soc. 9: 101–107

    Google Scholar 

  • Mallet, A. L., Freeman, K. R., Dickie, L. M. (1986). The genetics of production characters in the blue mussel Mytilus edulis I. A preliminary analysis. Aquaculture, Amsterdam 57: 133–140

    Google Scholar 

  • Manzi, J. J. (1985). Clam aquaculture. In: Hunter, J. V., Brown, E. E. (eds.) Crustacean and mollusk aquaculture in the United States. AVI Publications, Westport, p. 275–310

    Google Scholar 

  • Mitchell-Olds, T., Rutledge, J. J. (1986). Quantitative genetics in natural plant populations: a review of the theory. Am. Nat. 127: 379–402

    Google Scholar 

  • Newkirk, G. (1978). Interaction of genotype and salinity in larvae of the oyster Crassostrea virginica. Mar. Biol. 48: 227–234

    Google Scholar 

  • Newkirk, G., Haley, L. E., Dingle, J. (1981). Genetics of the blue mussel Mytilus edulis (L.): nonadditive genetic variation in larval growth rate. Can. J. Genet. Cytol. 23: 349–354

    Google Scholar 

  • Newkirk, G., Haley, L. E., Waugh, D. L., Doyle, R. (1977). Genetics of larval and spat growth rate in the oyster Crassostrea virginica. Mar. Biol. 41: 49–52

    Google Scholar 

  • Ockelmann, K. W. (1965). Development types in marine bivalves and their distribution along the Atlantic coast of Europe. Proc. 1st Eur malac. Congr. 1962: 25–35 [Cox, L. R., Peake, J. F. (eds.) Conchological Soc. of Gt Britain and Malacological Soc. of London]

  • Pechenik, J. A. (1987). Environmental influences on larval survival and development. In: Giese, A. C., Pearse, J. S., Pearse, V. B. (eds.) Reproduction of marine invertebrates, Vol. IX. Blackwell Scientific Publications, Palo Alto, p. 551–608

    Google Scholar 

  • Pennington, J. T., Rumrill, S. S., Chia, F-S. (1986). Stage-specific predation upon embryos and larvae of the Pacific sand dollar, Dendraster excentricus, by 11 species of common zooplanktonic predators. Bull. mar. Sci. 39: 234–240

    Google Scholar 

  • Raven, P. D. (1966). Morphogenesis: the analysis of molluscan development. Pergamon Press, Oxford

    Google Scholar 

  • Rawson, P. D., Hilbish, T. J. (1990). Heritability of juvenile shell growth for the hard clam Mercenaria mercenaria. Mar. Biol. 105: 429–436

    Google Scholar 

  • Rawson, P. D., Hilbish T. J. (1991). Genotype-environment interaction for juvenile growth in the hard clam Mercenaria mercenaria (L.). Evolution, Lawrence, Kansas 45: 1924–1935

    Google Scholar 

  • Shaw, R. G. (1987). Maximum likelihood approaches applied to quantitative genetics in natural populations. Evolution, Lawrence, Kansas 41: 812–826

    Google Scholar 

  • Sokal, R. R., Rohlf, F. J. (1980). Biometry. W. H. Freeman, New York

    Google Scholar 

  • Strathmann, M. F. (1987a). Reproduction and development of marine invertebrates of the northern Pacific coast. University of Washington Press, Seattle

    Google Scholar 

  • Strathmann, R. R. (1987b). Larval feeding. In: Giese, A. C., Pearse, J. S., Pearse, V. B. (eds.) Reproduction of marine invertebrates, Vol. IX. Blackwell Scientific Publications, Palo Alto, p.465–550

    Google Scholar 

  • Thorson, G. (1950). Reproduction and larval ecology of marine bottom invertebrates. Biol. Rev. 25: 1–45

    Google Scholar 

  • Vance, R. R. (1973a). On reproductive strategies in marine benthic invertebrates. Am. Nat. 107: 339–352

    Google Scholar 

  • Vance, R. R. (1973b). More on reproductive strategies of marine benthic invertebrates. Am. Nat. 107: 353–361

    Google Scholar 

  • Verdonk, N. H., van den Biggelaar, J. A. M. (1983). Early development and the formation of the germ layers. In: Verdonk, N. H., van den Biggelaar J. A. M., Tompa, A. S. (eds.) The Mollusca, Vol. 3, Development. Academic Press, New York, p. 91–122

    Google Scholar 

  • Via, S. (1984). The quantitative genetics of polyphagy in an insect herbivore. II. Genetic correlations in larval performance within and among host plants. Evolution, Lawrence, Kansas 38: 896–905

    Google Scholar 

  • Via, S., Lande, R. (1987). Evolution of genetic variability in a spatially heterogeneous environment: effects of genotype-environment interaction. Genet. Res. 49: 147–156

    Google Scholar 

  • Wethey, D. S. (1985). Local and regional variation in settlement and survival in the littoral barnacle Semibalanus balonoides (L.): patterns and consequences. In: Moore, P. G., Seed, R. (eds.) The ecology of rocky coasts. Hodder and Stoughton, London, p. 194–202

    Google Scholar 

  • Young, B. L. (1989). Settlement, early mortality, and growth of sessile marine invertebrates. Ph. D. dissertation. University of South Carolina, Columbia

    Google Scholar 

  • Young, C. M., Chia, F-S. (1987). Abundance and distribution of pelagic larvae as influences by predations, behavior, and hydrographic factors. In: Giese, A. C., Pearse, J. S., Pearse, V. B. (eds.) Reproduction of marine invertebrates, Vol. IX. Blackwell Scientific Publications, Palo Alto, p. 385–463

    Google Scholar 

  • Zimmerman, K. M., Pechenik, J. A. (1991). How do temperature and salinity affect relative rates of growth, morphological differentiation, and time to metamorphic competence in larvae of the marine gastropod Crepidula plana? Biol. Bull. mar. biol. Lab., Woods Hole 180: 372–386

    Google Scholar 

  • Zouros, E., Foltz, D. W. (1984). Possible explanations of heterozygote deficiency in bivalve molluscs. Malacologia 25: 583–591

    Google Scholar 

  • Zouros, E., Foltz, D. W. (1987). The use of allelic isozyme variation for the study of heterosis. Isozymes. Curr. Topics biol. Med. Res. 13: 1–59

    Google Scholar 

  • Zouros, E., Singh, S. M., Miles, H. E. (1980). Growth rate in oysters: an overdominant phenotype. Evolution, Lawrence, Kansas 34: 856–867

    Google Scholar 

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Contribution no. 964 from the Belle W. Baruch Institute for Marine Biology and Coastal Research

Communicated by J. Grassle, New Brunswick

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Hilbish, T.J., Winn, E.P. & Rawson, P.D. Genetic variation and covariation during larval and juvenile growth in Mercenaria mercenaria . Marine Biology 115, 97–104 (1993). https://doi.org/10.1007/BF00349390

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