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Mixed genetic and environmental sex determination in an androdioecious population of Mercurialis annua
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  • Original Article
  • Published: 01 January 1997

Mixed genetic and environmental sex determination in an androdioecious population of Mercurialis annua

  • John Pannell1 nAff2 

Heredity volume 78, pages 50–56 (1997)Cite this article

  • 1857 Accesses

  • 79 Citations

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Abstract

Mercurialis annua is a ruderal of pan-European distribution. In southern Spain, southern Portugal and northern Morocco, males coexist with monoecious (cosex) individuals at frequencies which vary between zero and about 30 per cent. Here, I report the results of two glasshouse experiments which aimed to characterize the mode of sex determination in one such androdioecious population. In a breeding experiment, cosexes isolated from males produced only cosexual progeny, whereas those allowed to mate with males produced both cosexual and male offspring. The results are consistent with a single-locus model of sex inheritance, with maleness determined by a dominant allele. In a density experiment, the frequency of males correlated positively with density, confirming field observations. Differential mortality or germination between the sexes was excluded by experimental design, so that the result supports the hypothesis of density-dependent gender choice. A negative correlation between density and the proportion of ‘late cosexes’ (males which turned cosexual late in their development), and the lack of any differences in the proportion of pure (unchanged) cosexes between density, suggest that only males were capable of sex change. This interpretation is consistent with the results of the breeding experiment, in which late cosexes occurred only in the offspring of cosexes allowed to mate with males. I argue that these findings help to explain the maintenance of androdioecy in M. annua.

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References

  • Armitage, P. 1971. Statistical Methods in Medical Research, 1st edn. Blackwell Scientific Publications, Oxford.

    Google Scholar 

  • Aronne, G, and Wilcock, C C. 1994. Reproductive characteristics and breeding system of shrubs in the Mediterranean region. Funct Ecol, 8, 69–76.

    Article  Google Scholar 

  • Baker, H G. 1955. Self-compatibility and establishment after ‘long-distance’ dispersal. Evolution, 9, 347–348.

    Google Scholar 

  • Baker, H G. 1967. Support for Baker's Law—as a rule. Evolution, 21, 853–856.

    Article  Google Scholar 

  • Charlesworth, D. 1984. Androdioecy and the evolution of dioecy. Biol J Linn Soc, 22, 333–348.

    Article  Google Scholar 

  • Charlesworth, D, and Charlesworth, B. 1978. A model for the evolution of dioecy and gynodioecy. Am Nat, 112, 975–997.

    Article  Google Scholar 

  • Charnov, E L. 1982. The Theory of Sex Allocation. Princeton University Press, Princeton, NJ.

    Google Scholar 

  • Durand, B. 1963. Le complexe Mercurialis annua L. s.l.: une étude biosystematique. Ann Sci Nat Bot, 12, 579–736.

    Google Scholar 

  • Durand, B, and Durand, R. 1991a. Male sterility and restored fertility in annual mercuries: relations with sex differentiation. Plant Sci, 80, 107–118.

    Article  CAS  Google Scholar 

  • Durand, B, and Durand, R. 1991b. Sex determination and reproductive organ differentiation in Mercurialis. Plant Sci, 80, 49–66.

    Article  Google Scholar 

  • Durand, R, and Durand, B. 1992. Dioecy, monoecy, polyploidy and speciation in annual Mercuries. Bull Soc Bot Fr Lett Bot, 139, 377–399.

    Google Scholar 

  • Freeman, D C, and Vitale, J J. 1985. The influence of environment on the sex ratio and fitness of spinach. Bot Gaz, 146, 137–142.

    Article  Google Scholar 

  • Fritsch, P, and Rieseberg, L H. 1992. High outcrossing rates maintain male and hermaphrodite individuals in populations of the flowering plant Datisca glomerata. Nature, 359, 633–636.

    Article  Google Scholar 

  • Gouyon, P-H, and Couvet, D. 1987. A conflict between two sexes, females and hermaphrodites. In: Stearns, S. C. (ed.) The Evolution of Sex and its Consequences, pp. 245–261. Birkhäuser Verlag, Basel.

    Chapter  Google Scholar 

  • Irish, E E, and Nelson, T. 1989. Sex determination in monoecious and dioecious plants. Pl Cell, 1, 737–744.

    Article  Google Scholar 

  • Jarne, P, and Charlesworth, D. 1993. The evolution of the selfing rate in functionally hermaphrodite plants and animals. Ann Rev Ecol Syst, 24, 441–466.

    Article  Google Scholar 

  • Kohn, J R. 1989. Sex ratio, seed production, biomass allocation, and the cost of female function in Curcurbita foetidissima HBK (Curcurbitaceae). Evolution, 43, 1424–1434.

    Article  Google Scholar 

  • Lepart, J, and Dommée, B. 1992. Is Phillyrea angustifolia L. (Oleaceae) an androdioecious species? Bot J Linn Soc, 108, 375–387.

    Article  Google Scholar 

  • Liston, A, Rieseberg, L H, and Elias, T S. 1990. Functional androdioecy in the flowering plant Datisca glomerata. Nature, 343, 641–642.

    Article  Google Scholar 

  • Lloyd, D G. 1975. The maintenance of gynodioecy and androdioecy in angiosperms. Genetica, 45, 325–339.

    Article  Google Scholar 

  • Lloyd, D G, and Bawa, K S. 1984. Modification of the gender of seed plants in varying conditions. Evol Biol, 17, 255–336.

    Article  Google Scholar 

  • Louis, J P, Augur, C, and Teller, G. 1990. Cytokinins and differentiation processes in Mercurialis annua. Genetic regulation, regulations with auxins, indoleacetic acid oxidases, and sexual expression patterns. Pl Physiol, 94, 1535–1541.

    Article  CAS  Google Scholar 

  • Love, A, and Kapoor, B M. 1967. A chromosome atlas of the collective genus Rumex. Cytologia, 32, 328–342.

    Article  Google Scholar 

  • Meagher, T R. 1988. Sex determination in plants. In: Lovett Doust, J. and Lovett Doust, L. (eds) Plant Reproductive Ecology: Patterns and Strategies, pp. 125–138. Oxford University Press, New York.

    Google Scholar 

  • Otto, S P, Sassaman, C, and Feldman, M W. 1993. Evolution of sex determination in the conchostracan shrimp Eulimnadia texana. Am Nat, 141, 327–337.

    Article  Google Scholar 

  • Pannell, J R. 1995. Models of Androdioecy and Studies on Mercurialis annua L. D.Phil. Thesis, University of Oxford.

    Google Scholar 

  • Pannell, J R. 1997a. Variation in sex ratios and sex allocation in androdioecious Mercurialis annua. J Ecol, (in press).

  • Pannell, J R. 1997b. Widespread functional androdioecy in Mercurialis annua L. (Euphorbiaceae). Biol J Linn Soc, (in press).

  • Pannell, J R. 1997c. The maintenance of gynodioecy and androdioecy in a metapopulation. Evolution, (in press).

  • Reboud, X, and Zeyl, C. 1994. Organelle inheritance in plants. Heredity, 72, 132–140.

    Article  Google Scholar 

  • Sakai, A K, and Weller, S G. 1991. Ecological aspects of sex expression in subdioecious Schiedea globosa (Caryo-phyllaceae). Am J Bot, 78, 1280–1288.

    Article  Google Scholar 

  • Sassaman, C. 1989. Inbreeding and sex ratio variation in female-biased populations of a clam shrimp, Eulimnadia texana. Bull Mar Sci, 45, 425–432.

    Google Scholar 

  • Sassaman, C. 1991. Sex ratio variation in female-biased populations of Notostracans. Hydrobiologia, 212, 169–179.

    Article  Google Scholar 

  • Sassaman, C, and Weeks, S C. 1993. The genetic mechanism of sex determination in the conchostracan shrimp Eulimnadia texana. Am Nat, 141, 314–328.

    Article  CAS  Google Scholar 

  • Traveset, A. 1994. Reproductive biology of Phillyrea angustifolia L. (Oleaceae) and effect of galling-insects on its reproductive output. Bot J Linn Soc, 114, 153–166.

    Article  Google Scholar 

  • Tutin, T G, Heywood, V H, Burges, N A, Moore, D M, Valentine, D H, Walters, S M, and Webb, D A. 1968. Flora Europaea, vol. 2. Cambridge University Press, Cambridge.

    Google Scholar 

  • Valdes, B, Talavera, S, and Fernandez-Galiano, E. 1987. Flora Vascular de Andalucía Occidental, vol. 2. Ketres Editora, Barcelona.

    Google Scholar 

  • Van Damme, J M M. 1991. A restorer gene in gynodioe-cious Plantago coronopus subject to selection in the gametophytic and seedling stage. Heredity, 66, 19–27.

    Article  Google Scholar 

  • Westergaard, M. 1958. The mechanism of sex determination in flowering plants. Adv Genet, 9, 217–281.

    Article  CAS  Google Scholar 

Download references

Author information

Author notes
  1. John Pannell

    Present address: Department of Botany, University of Toronto, 25 Willcocks Street, Toronto, Ont., Canada, M55 3B2

Authors and Affiliations

  1. Department of Plant Sciences, University of Oxford, South Parks Road, Oxford, OX1 3RB, UK

    John Pannell

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  1. John Pannell
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Cite this article

Pannell, J. Mixed genetic and environmental sex determination in an androdioecious population of Mercurialis annua. Heredity 78, 50–56 (1997). https://doi.org/10.1038/hdy.1997.6

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  • Received: 19 January 1996

  • Issue date: 01 January 1997

  • DOI: https://doi.org/10.1038/hdy.1997.6

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Keywords

  • androdioecy
  • dioecy
  • reproductive assurance
  • sex change
  • sex choice
  • sexual dimorphism

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