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Constancy of population parameters for life history and floral traits in Raphanus sativus L. I. Norms of reaction and the nature of genotype by environment interactions
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  • Original Article
  • Published: 01 October 1991

Constancy of population parameters for life history and floral traits in Raphanus sativus L. I. Norms of reaction and the nature of genotype by environment interactions

  • Susan J Mazer1 &
  • Charles T Schick1 

Heredity volume 67, pages 143–156 (1991)Cite this article

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Abstract

We observed norms of reaction for life history and floral traits in Raphanus sativus L. (wild radish: Brassicaceae) among genotypes raised in three planting densities. In the greenhouse, we used a nested breeding design to produce F1 seed representing 60 maternal plants and 15 pollen donors grown from field-collected seed. Eighteen hundred seeds were grown in three planting densities in an experimental garden. For each individual, we recorded survivorship, germination date, flowering date, petal area, ovule number, pollen production, and the mode of individual pollen grain volume/ flower. Planting density had a strong effect on survivorship, but differential mortality among genotypes was not density-specific. Two-way ANOVAS (block and density as class variables) were conducted on each paternal sibship to detect significant differences among densities with respect to mean phenotype. Among the 15 paternal genotypes, 12 exhibited significantly faster germination in the high-density plots. Three paternal families exhibited significantly delayed flowering at high-density. Two paternal families exhibited significant effects of density on petal area, but in opposite directions. Two paternal families had significantly lower ovule production at high-density. No paternal families exhibited significant effects of density on pollen production or pollen-grain volume. Strong differences among genotypes with respect to the effects of density on phenotype indicate genetic variation in the plastic response to density for these traits. Three-way ANOVAS of each density treatment measured the effects of block, paternal family and maternal family on phenotype; significant paternal effects indicated the presence of significant additive genetic variance ( VA) in the measured trait. The ability to detect VA and maternal effects nested within paternal genotypes in most of these traits was density-specific.

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References

  • Becker, W A. 1984. Manual of Quantitative Genetics. Academic Enterprises Pullman, Washington. 4th edn.

    Google Scholar 

  • Comstock, R E, and Robinson, H F. 1948. The components of genetic variance in populations of biparental progenies and their use in estimating the average degree of dominance. Biometrics, 4, 254–266.

    Article  CAS  Google Scholar 

  • Devlin, B. 1988. The effects of stress on reproductive characters of Lobelia cardinalis. Ecology, 69, 1716–1720.

    Article  Google Scholar 

  • Hallauer, A R, and Miranda, J B. 1981. Quantitative Genetics in Maize Breeding. Iowa State University Press, Ames, Iowa.

    Google Scholar 

  • Lande, R. 1976. Natural selection and random genetic drift in phenotypic evolution. Evolution, 30, 314–334.

    Article  Google Scholar 

  • Lande, R. 1979. Quantitative genetic analysis of multivariate evolution applied to brain: body size allometry. Evolution, 33, 402–416.

    Article  Google Scholar 

  • Lande, R. 1980. Genetic variation and phenotypic evolution during allopatric speciation. Am Nat, 116, 463–479.

    Article  Google Scholar 

  • Lewis, D, Verma, S C, and Zuberi, M I. 1988. Gametophyticsporophytic incompatibility in the Cruciferae — Raphanussativus. Heredity, 61, 355–366.

    Article  Google Scholar 

  • Marshall, D L, and Ellstrand, N C. 1986. Sexual selection in Raphanus sativus: experimental data on non-random fertilization, maternal choice, and consequences of multiple paternity. Am Nat, 127, 446–461.

    Article  Google Scholar 

  • Mazer, S J. 1987a. The quantitative genetics of life history and fitness components in Raphanus raphanistrum L. (Brassicaceae): ecological and evolutionary consequences of seed-weight variation. Am Nat, 130, 891–914.

    Article  Google Scholar 

  • Mazer, S J. 1987b. Parental effects on seed development and seed yield in Raphanus raphanistrum: implications for natural and sexual selection. Evolution, 41, 355–371.

    PubMed  Google Scholar 

  • Panetsos, C A, and Baker, H G. 1967. The origin of variation in ‘wild’ Raphanus sativus (Cruciferae) in California. Genetica, 38, 243–274.

    Article  Google Scholar 

  • Putrament, A. 1960. Studies in self-sterility in Raphanus sativus (L.) var. radicula (DC) Act Soc Bot Pol, XXIV, 289–313.

    Google Scholar 

  • Sas Institute, Inc., 1987. SAS/STAT Guide for Personal Computers, Version 6 Edition. SAS Institute Inc., Cary, North Carolina.

  • Schlichting, C D. 1986. The evolution of phenotypic plasticity in plants. Ann Rev Ecol Syst, 17, 667–693.

    Article  Google Scholar 

  • Service, P M, and Rose, M R. 1985. Genetic covariation among life-history components: the effect of novel environments. Evolution, 39, 943–945.

    Article  Google Scholar 

  • Shaw, R G. 1986. Response to density in a wild population of the perennial herb Salvia lyrata: variation among families. Evolution, 40, 492–505.

    PubMed  Google Scholar 

  • Stanton, M L. 1984a. Developmental and genetic sources of seed weight variation in Raphanus raphanistrum L. (Brassicaceae). Am J Bot, 71, 1090–1098.

    Article  Google Scholar 

  • Stanton, M L. 1985. Seed size and emergence time within a stand of wild radish (Raphanus raphanistrum L.): the establishment of a fitness hierarchy. Oecologia, 67, 524–531.

    Article  Google Scholar 

  • Stanton, M L. 1987a. The reproductive biology of petal color variants in wild populations of Raphanus sativus L.: I. Pollinator response to color morphs. Am J Bot, 74, 178–187.

    Article  Google Scholar 

  • Stanton, M L. 1987b. The reproductive biology of petal color variants in wild populations of Raphanus sativus L.: II. Factors limiting seed production. Am J Bot, 74, 188–196.

    Article  Google Scholar 

  • Turelli, M. 1988. Phenotypic evolution, constant covariances and the maintenance of additive variance. Evolution, 42, 1342–1347.

    Article  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Westerman, J M. 1971a. Genotype-environment interaction and developmental regulation in Arabidopsis thaliana. II. Inbred lines; analysis. Heredity, 26, 93–106.

    Article  Google Scholar 

  • Westerman, J M. 1971b. Genotype-environment interaction and developmental regulation in Arabidopsis thaliana. III. Inbred lines; analysis of response to photoperiod. Heredity, 26, 373–382.

    Article  Google Scholar 

  • Westerman, J M. 1971. Genotype-environment interaction and developmental regulation in Arabidopsis thaliana. IV. Wild material; analysis. Heredity, 26, 383–395.

    Article  Google Scholar 

  • Westerman, J M, and Lawrence, M J. 1970. Genotype-environment interaction and developmental regulation in Arabidopsis thaliana. I. Inbred lines; description. Heredity, 25, 609–627.

    Article  Google Scholar 

  • Young, H J, and Stanton, M L. 1990. Influence of environmental quality on pollen competitive ability in wild radish. Science, 248, 1631–1633.

    Article  CAS  Google Scholar 

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Authors and Affiliations

  1. Department of Biological Sciences, University of California, Santa Barbara, 93106, California, USA

    Susan J Mazer & Charles T Schick

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  1. Susan J Mazer
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  2. Charles T Schick
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Mazer, S., Schick, C. Constancy of population parameters for life history and floral traits in Raphanus sativus L. I. Norms of reaction and the nature of genotype by environment interactions. Heredity 67, 143–156 (1991). https://doi.org/10.1038/hdy.1991.74

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  • Received: 11 September 1990

  • Issue date: 01 October 1991

  • DOI: https://doi.org/10.1038/hdy.1991.74

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Keywords

  • genotype-environment interaction
  • heritability
  • norms of reaction
  • phenotypic plasticity
  • Raphanus

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