2013
DOI: 10.1086/671233
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The Contributions of Premating and Postmating Selection Episodes to Total Selection in Sex-Role-Reversed Gulf Pipefish

Abstract: Empirical studies of sexual selection often focus on events occurring either before or after mating but rarely both and consequently may fail to discern the relative magnitudes and interactions of premating and postmating episodes of selection. Here, we simultaneously quantify premating and postmating selection in the sex-role-reversed Gulf pipefish by using a microsatellite-based analysis of parentage in experimental populations. Female pipefish exhibited an opportunity for selection (I) of 1.64, which was hi… Show more

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Cited by 42 publications
(61 citation statements)
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“…We expected to find a signature of selection because Gulf pipefish females are known to be under strong sexual selection (Jones et al 2001;Rose et al 2013;Flanagan et al 2014), and we did find higher F ST values in the mothers-females comparison than between males and females. We expected to find a signature of selection because Gulf pipefish females are known to be under strong sexual selection (Jones et al 2001;Rose et al 2013;Flanagan et al 2014), and we did find higher F ST values in the mothers-females comparison than between males and females.…”
Section: Discussionmentioning
confidence: 66%
See 1 more Smart Citation
“…We expected to find a signature of selection because Gulf pipefish females are known to be under strong sexual selection (Jones et al 2001;Rose et al 2013;Flanagan et al 2014), and we did find higher F ST values in the mothers-females comparison than between males and females. We expected to find a signature of selection because Gulf pipefish females are known to be under strong sexual selection (Jones et al 2001;Rose et al 2013;Flanagan et al 2014), and we did find higher F ST values in the mothers-females comparison than between males and females.…”
Section: Discussionmentioning
confidence: 66%
“…However, we identified a much larger number of significant RAD loci in the males-females comparison than in the comparison of inferred maternal alleles and females. Since sexual selection is known to act on females and not males in S. scovelli (Rose et al 2013), a trade-off between traits could explain genome-wide allele frequency differences between the sexes. These results suggest that differential selection on males and females may be having a pervasive effect throughout the genome.…”
Section: Discussionmentioning
confidence: 99%
“…In short-term experiments, and (imposed) semelparous situations, one can separate pre- from post-copulatory components of sexual selection by looking at the residual variance in reproductive success, i.e. the variance not explained by mating success (this residual can be explained by post-copulatory processes: Rose et al, 2013a, 2013b; Pélissié et al, 2014; Janicke et al, 2015). This is no longer straight-forward in a dataset from a longer running experiment where everyone has mated repeatedly with everyone else and sperm from those previous matings is still in storage.…”
Section: Discussionmentioning
confidence: 99%
“…So far, experiments were generally only performed over a short time frame, as pointed out earlier; e.g. Pélissié et al, 2012, Pélissié et al, 2014; Anthes et al, 2010; Collet et al, 2012; Rose et al, 2013a; but see Turnell and Shaw, 2015). …”
Section: Methodsmentioning
confidence: 99%
“…Oocyte size seems to be a good explanation for this preference, as wider stripes indicate larger oocytes, which are known to be more nutritious (Goncalves et al., ). Size is certainly another trait selected by syngnathid males (Berglund et al., , ; Mattle & Wilson, ; Paczolt & Jones, ; Rose, Paczolt, & Jones, ), including S. abaster (Silva et al., ), as it is usually positively related to female fecundity (Braga Goncalves et al., ). However, as we verified in S. abaster , size can at times be only indirectly related to female quality, both through stripe width and trunk broadness.…”
Section: Discussionmentioning
confidence: 99%