Summary
The following parameters affecting the frequency of male and female plants in sexually dimorphic Angiosperms are defined: relative fecundity (as seed parent), F, differential survival, S, and gamete success, G, all as male/female quotients, and the probability of fertilisation of ovules on female plants, in terms of the number of pollinator visits to the flowers, x.
Four different modes of inheritance of gynodioecy and dioecy are examined:
-
a)
Heterozygous female model—female Mm, male mm.
-
b)
Dual male model—female mm, male MM and Mm.
-
c)
Heterozygous male model—female mm, male Mm only.
-
d)
Cytoplasmic inheritance.
The equilibrium frequencies of females and (for three models) the rates of change in female frequency per generation at non-equilibrium frequencies are expressed in terms of the controlling parameters.
The conditions necessary for sexual dimorphism and the changes in frequencies of the sex genotypes as the number of pollinator visits increase and the relative seed fecundity decreases towards zero (dioecy) are derived for each model.
Differential survival of the sexes (and differential gamete success in the heterozygous male model) cause an increase at equilibrium in the sex surviving more frequently or the sex derived from the more successful gamete. In a dioecious population, the ratio of the sexes is equal to their relative survival or their relative gamete success.
Populations at non-equilibrium frequencies return more rapidly to equilibrium with the heterozygous male model than with the heterozygous female and cytoplasmic models. In the extreme case when females are lost from a population, with the heterozygous female and cytoplasmic models extinction or loss of sexual dimorphism occurs, but with the heterozygous male and dual male models sexual dimorphism is regenerated. The ability of systems with heterozygous males to regenerate dimorphism may explain the prevalence of such systems in both gynodioecious and dioecious populations.
Similar content being viewed by others
Article PDF
References
Allen, C E. 1940. The genotypic basis of sex-expression in Angiosperms. Biol Rev, 6, 227–300.
Baker, H G. 1966. The evolution of floral heteromorphism and gynodioecism in Silene maritima. Heredity, 21, 689–692.
Burrows, C J. 1960. Studies in Pimelea. I. The breeding system. Trans Roy Soc New Zeal, 88, 29–45.
Carlquist, C. 1966. The biota of long-distance dispersal. IV. Genetic systems in the floras of oceanic islands. Evolution, 20, 433–455.
Connor, H E. 1965a. Breeding systems in New Zealand grasses. V. Naturalised species of Cortaderia. New Zeal Jour Bot, 3, 17–23.
Connor, H E. 1965b. Breeding systems in New Zealand grasses. VI. Control of gynodioecism in Cortaderia richardii (Endl.) Zotov. New Zeal Jour Bot, 3, 233–242.
Correns, C. 1928. Bestimmung, Vererbung und Verteilung des Geschlechtes bei den höheren Pflanzen. Handb Vererbungsw, 2, 1–138.
East, E M. 1934. The nucleus-plasma problem II. Amer Nat, 68, 402–439.
Godley, E J. 1963. Breeding systems in New Zealand plants. 2. Genetics of the sex forms in Fuschia procumbens. New Zeal Jour Bot, 1, 48–52.
Godley, E J. 1964. Breeding systems in New Zealand plants. 3. Sex ratios in some natural populations. New Zeal Jour Bot, 2, 205–212.
Grewal, M S, and Ellis, J R. 1972. Sex determination in Potentilla fruticosa. Heredity, 29, 359–362.
Jain, S K. 1961. On the possible adaptive significance of male sterility in predominantly inbreeding populations. Genetics, 46, 1237–1240.
Lewis, D. 1941. Male sterility in natural populations of hermaphrodite plants. New Phytol, 40, 56–63.
Lewis, D. 1942. The evolution of sex in flowering plants. Biol Rev, 17, 46–67.
Lewis, D, and Crowe, L K. 1956. The genetics and evolution of gynodioecy. Evolution, 10, 115–125.
Linnert, G. 1958. Kernesteuerte Gynodiõzie bei Salvia memorosa. Zeit indukt Abst Vererb, 89, 36–51.
Lloyd, D G. 1972. Breeding systems in Cotula L. (Gompositae, Anthemideae). I. The array of monoclinous and diclinous systems. New Phytol, 71, 1181–1194.
Lloyd, D G. 1973a. Sex ratios in sexually dimorphic Umbelliferae. Heredity, 31.
Lloyd, D G. 1973b. Female-predominant sex ratios in Angiosperms. Heredity, 31, 35–44.
Löve, A. 1957. Sex determination in Rumex. Proc Genet Soc Canada, 2, 31–36.
McCusker, A. 1962. Gynodioecism in Leucopogon melaleucoides A. Gunn. Proc Linn Soc New South Wales, 87, 286–289.
Mulcahy, D L. 1967a. Optimal sex ratio in Silene alba. Heredity, 22, 411–423.
Mulcahy, D L. 1967b. The selective advantage of staminate heterogamety. Taxon, 16, 280–283.
Ross, M D. 1969. Digenic inheritance of male sterility in Plantago lanceolata. Can Jour Genet Cytol, 11, 729–744.
Ross, M D. 1970. Evolution of dioecy from gynodioecy. Evolution, 24, 827–828.
Ross, M D, and Shaw, R F. 1971. Maintenance of male sterility in plant populations. Heredity, 26, 1–8.
Storey, W B. 1953. Genetics of the papaya. Jour Hered, 44, 70–78.
Smith, B W. 1963. The mechanism of sex determination in Rumex hastatulus. Genetics, 48, 1265–1288.
Valdeyron, G. 1967. Sur le système génétique du figuier, Ficus carica L.: essai d'interprétation evolutive. Ann Inst Nat Agron, 5, 1–167.
Westergaard, M. 1958. The mechanism of sex determination in dioecious flowering plants. Adv Genet, 9, 217–281.
Williams, W. 1964. Genetical principles and plant breeding. Blackwell, Oxford.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Lloyd, D. Theoretical sex ratios of dioecious and gynodioecious angiosperms. Heredity 32, 11–34 (1974). https://doi.org/10.1038/hdy.1974.2
Received:
Issue date:
DOI: https://doi.org/10.1038/hdy.1974.2
This article is cited by
-
A case of gender equality: absence of sex-related costs in a dioecious tropical forest tree species
Plant Ecology (2021)
-
Low seed fertility of hermaphrodites is maintained in a gynodioecious species throughout the distribution range in Japan
Plant Systematics and Evolution (2021)
-
Stigmas arrangement, reproductive system, and maternal reproductive success in two species of Stigmaphyllon (Malpighiaceae): does pollinator size matter?
Plant Ecology (2021)
-
Seed germination of gynodioecious species: theoretical considerations and a comparison of females and hermaphrodites
Planta (2020)
-
Sex ratio of dioecious Allanblackia stuhlmannii (Engl.) Engl. in Tanzanian Usambara forests and farmlands
Agroforestry Systems (2020)


