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The relationship between pollen grain size and progeny gender in dioecious Silene latifolia (Caryophyllaceae)

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Summary

Experiments and observations conducted during the past 90 years have provided conflicting evidence concerning the existence of a size difference between pollen grains containing an X chromosome (female-determining) and those containing a Y chromosome (maledetermining) in dioecious Silene latifolia. Were such a size difference to exist, this might explain, at least in part, the observation that X-bearing pollen tubes reach the ovary more quickly, on average, than Y-bearing pollen tubes. We tested for such a size difference by separating pollen collected from single anthers into three size classes: small, large, and random. Fruit set (number of pollinated flowers that set fruit) and seed set (number of seeds per capsule) did not differ for these three pollination treatments. Progeny sex ratios resulting from these three pollen size classes also did not differ significantly. Thus, pollen grain size is not affected by which of the two sex chromosomes is present. Our experiment is the first direct test of this relationship. Based on our results, size differences should not be invoked to explain competitive differences in male- and female-determining microgametophytes.

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References

  • Allen CE (1940) The genotypic basis of sex-expression in angiosperms. Bot Rev 6:227–300

    Google Scholar 

  • Blackburn KB (1923) Sex chromosomes in plants. Nature 112:687–688

    Google Scholar 

  • Correns C (1917) Ein Fall experimenteller Verschiebung des Geschlechtsverhältnisses. Sitzungsber K Preuss Akad Wiss 685–717

  • Correns C (1918) Fortsetzung der Versuche zur experimentellen Verschiebung des Geschlechtsverhältnisses. Sitzungsber K Preuss Akad Wiss 1175–1200

  • Correns C (1922) Alkohol und Zahlenverhältnis der Geschlechter bei einer getrenntgeschlechtigen Pflanze (Melandrium). Naturwissenschaften 10:1049–1052

    Google Scholar 

  • Correns C (1928) Bestimmung, Vererbung und Verteilung des Geschlechtes bei den höheren Pflanzen. Handb Vererbungswiss 2:1–138

    Google Scholar 

  • Frick B, Cavers PB (1989) Aberrations in sex expression in Silene latifolia. Am Nat 134:562–573

    Google Scholar 

  • Lawrence CW (1963a) Genetic studies on wild populations of Melandrium. I. Chromosome behaviour. Heredity 18:135–148

    Google Scholar 

  • Lawrence CW (1963b) Genetic studies on wild populations of Melandrium. II. Flowering time and plant weight. Heredity 18:149–163

    Google Scholar 

  • Löve D (1940) Some studies on sex-determination in Melandrium rubrum. Sven Bot Tidskr 34:234–247

    Google Scholar 

  • McNeill J, Crompton CW (1978) Pollen dimorphism in Silene alba (Caryophyllaceae). Can J Bot 56:1280–1286

    Google Scholar 

  • Mangelsdorf PC (1932) Mechanical separation of gametes in maize. J Hered 23:289–295

    Google Scholar 

  • Meagher TR (1988) Sex determination in plants. In: Lovett Doust J, Lovett Doust L (eds) Plant reproductive ecology. Oxford University Press, New York Oxford, pp 125–138

    Google Scholar 

  • Nigtevecht G Van (1966) Genetic studies in dioecious Melandrium. II. Sex determination in Melandrium album and Melandrium dioicum. Genetica 37:307–344

    Google Scholar 

  • Niizeki M, Saito K (1988) Increasing the transmission rate of the extra chromosome in a trisomic Nicotiana sylvestris by modifying the means of pollination. Theor Appl Genet 76:891–896

    Google Scholar 

  • Peterson PA, Munson A (1962) B chromosomes and pollen size in maize. J Iowa Acad Sci 69:155–159

    Google Scholar 

  • Prentice HC (1987) Analysis of the clinal variation pattern in Silene latifolia (Caryophyllaceae) pollen morphology. Plant Syst Evol 156:5–11

    Google Scholar 

  • Prentice HC, Mastenbroek O, Berendsen W, Hogeweg P (1984) Geographic variation in the pollen of Silene latifolia (S. alba, S. pratensis): a quantitative morphological analysis of population data. Can J Bot 62:1259–1267

    Google Scholar 

  • Santos JK (1923) Differentiation among chromosomes in Elodea. Bot Gaz 75:42–59

    Google Scholar 

  • Santos JK (1924) Determination of sex in Elodea. Bot Gaz 77:353–376

    Google Scholar 

  • SAS Institute (1987) SAS/STAT guide for personal computers, version 6. Cary, NC

  • Singleton WR, Mangelsdorf PC (1940) Gametic lethals on the fourth chromosome of maize. Genetics 25:366–390

    Google Scholar 

  • Sinoto Y (1929) Chromosome studies in some dioecious plants with special reference to the allosomes. Cytologia 1:109–191

    Google Scholar 

  • Tischler G (1925) Ein Beitrag zum Verständnis des Certations-Problems bei Melandrium. Planta 1:332–341

    Google Scholar 

  • Warmke HE (1946) Sex determination and sex balance in Melandrium. Am J Bot 33:648–660

    Google Scholar 

  • Warmke HE, Blakeslee AF (1939) Sex mechanism in polyploids of Melandrium. Science 89:391–392

    Google Scholar 

  • Westergaard M (1958) The mechanism of sex determination in dioecious flowering plants. Adv Genet 9:217–281

    Google Scholar 

  • Winge O (1923) On sex chromosomes, sex determination, and preponderance of females in some dioecious plants. C R Trav Lab Carlsberg 15:1–25

    Google Scholar 

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Carroll, S.B., Mulcahy, D.L. The relationship between pollen grain size and progeny gender in dioecious Silene latifolia (Caryophyllaceae). Sexual Plant Reprod 4, 203–207 (1991). https://doi.org/10.1007/BF00190006

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