Literature DB >> 24854170

Temporal variation in phenotypic gender and expected functional gender within and among individuals in an annual plant.

Emily J Austen1, Arthur E Weis2.   

Abstract

BACKGROUND AND AIMS: Adaptive explanations for variation in sex allocation centre on variation in resource status and variation in the mating environment. The latter can occur when dichogamy causes siring opportunity to vary across the flowering season. In this study, it is hypothesized that the widespread tendency towards declining fruit-set from first to last flowers on plants can similarly lead to a varying mating environment by causing a temporal shift in the quality (not quantity) of siring opportunities.
METHODS: A numerical model was developed to examine the effects of declining fruit-set on the expected male versus female reproductive success (functional gender) of first and last flowers on plants, and of early- and late-flowering plants. Within- and among-plant temporal variation in pollen production, ovule production and fruit-set in 70 Brassica rapa plants was then characterized to determine if trends in male and female investment mirror expected trends in functional gender. KEY
RESULTS: Under a wide range of model conditions, functional femaleness decreased sharply in the last flowers on plants, and increased from early- to late-flowering plants in the population. In B. rapa, pollen production decreased more rapidly than ovule production from first to last flowers, leading to a within-plant increase in phenotypic femaleness. Among plants, ovule production decreased from early- to late-flowering plants, causing a temporal decrease in phenotypic femaleness.
CONCLUSIONS: The numerical model confirmed that declining fruit-set can drive temporal variation in functional gender, especially among plants. The discrepancy between observed trends in phenotypic gender in B. rapa and expected functional gender predicted by the numerical model does not rule out the possibility that male reproductive success decreases with later flowering onset. If so, plants may experience selection for early flowering through male fitness.
© The Author 2014. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  Brassica rapa; flowering time; fruit-set; hermaphrodite; hierarchical regression; ovule; phenology; phenotypic gender; pollen; sex allocation; within-plant variation

Mesh:

Year:  2014        PMID: 24854170      PMCID: PMC4071105          DOI: 10.1093/aob/mcu087

Source DB:  PubMed          Journal:  Ann Bot        ISSN: 0305-7364            Impact factor:   4.357


  14 in total

1.  Floral plasticity in an iteroparous plant: the interactive effects of genotype, environment, and ontogeny in Campanula rapunculoides (Campanulaceae).

Authors:  D W Vogler; S Peretz; A G Stephenson
Journal:  Am J Bot       Date:  1999-04       Impact factor: 3.844

2.  Temporal floral sex allocation in protogynous Aquilegia yabeana contrasts with protandrous species: support for the mating environment hypothesis.

Authors:  Shuang-Quan Huang; Lu-Lu Tang; Qian Yu; You-Hao Guo
Journal:  Evolution       Date:  2004-05       Impact factor: 3.694

3.  Rapid evolution of flowering time by an annual plant in response to a climate fluctuation.

Authors:  Steven J Franks; Sheina Sim; Arthur E Weis
Journal:  Proc Natl Acad Sci U S A       Date:  2007-01-12       Impact factor: 11.205

4.  Temporal variation in the pollen:ovule ratios of Clarkia (Onagraceae) taxa with contrasting mating systems: field populations.

Authors:  V A Delesalle; S J Mazer; H Paz
Journal:  J Evol Biol       Date:  2007-11-12       Impact factor: 2.411

Review 5.  Genetics and evolution of function-valued traits: understanding environmentally responsive phenotypes.

Authors:  John R Stinchcombe; Mark Kirkpatrick
Journal:  Trends Ecol Evol       Date:  2012-08-14       Impact factor: 17.712

Review 6.  Review. The strength and genetic basis of reproductive isolating barriers in flowering plants.

Authors:  David B Lowry; Jennifer L Modliszewski; Kevin M Wright; Carrie A Wu; John H Willis
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2008-09-27       Impact factor: 6.237

7.  Genetic variation in flowering time induces phenological assortative mating: quantitative genetic methods applied to Brassica rapa.

Authors:  Arthur E Weis; Tanya M Kossler
Journal:  Am J Bot       Date:  2004-06       Impact factor: 3.844

8.  Modification of phenotypic and functional gender in the monoecious Arum italicum (Araceae).

Authors:  M Méndez
Journal:  Am J Bot       Date:  1998-02       Impact factor: 3.844

Review 9.  Meta-analysis of phenotypic selection on flowering phenology suggests that early flowering plants are favoured.

Authors:  Miguel A Munguía-Rosas; Jeff Ollerton; Victor Parra-Tabla; J Arturo De-Nova
Journal:  Ecol Lett       Date:  2011-02-17       Impact factor: 9.492

10.  Variation in floral sex allocation in Polygonatum odoratum (Liliaceae).

Authors:  Javier Guitián; Mónica Medrano; José E Oti
Journal:  Ann Bot       Date:  2004-07-26       Impact factor: 4.357

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