» Articles » PMID: 34367658

Quantifying the Costs of Pre- and Postcopulatory Traits for Males: Evidence That Costs of Ejaculation Are Minor Relative to Mating Effort

Overview
Journal Evol Lett
Specialty Biology
Date 2021 Aug 9
PMID 34367658
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Although it is widely stated that both mating behavior and sperm traits are energetically costly for males, we currently lack empirical estimates of the costs to males of pre- versus postcopulatory investments. Such estimates require the experimental separation of the act of mating from that of ejaculation, which is a nontrivial logistical challenge. Here, we overcome this challenge using a novel morphological manipulation (gonopodium tip ablation) in the eastern mosquitofish () to tease apart investment in mating effort from that in sperm replenishment following ejaculation. We quantified the relative cumulative costs of investing in mating effort and ejaculation by comparing somatic traits and reproductive performance among three types of males: ablated males that could attempt to mate but not ejaculate; unablated males that could both mate ejaculate; and control males that had no access to females. We show that, after eight weeks, mating investment significantly reduces both body growth and immunocompetence and results in a significant decline in mating effort. In contrast, cumulative investment into sperm replenishment following ejaculation has few detectable effects that are only apparent in smaller males. These minor costs occur despite the fact that has very high levels of sperm competition and multiple mating by both sexes, which is usually associated with elevated levels of sperm production. Crucially, our study is the first, to our knowledge, to experimentally compare the relative costs of pre- and postcopulatory investment on components of male fitness in a vertebrate.

Citing Articles

Differences in adult nutritional requirements impact the population growth and survival of two related species of rice leaffolders to produce interspecific differentiation.

Ding L, Guo J, Yang Y, Lu Y, Xie X, Lu Z Sci Rep. 2024; 14(1):17200.

PMID: 39060323 PMC: 11282227. DOI: 10.1038/s41598-024-66512-0.


Male allocation to ejaculation and mating effort imposes different life history trade-offs.

Chung M, Fox R, Jennions M PLoS Biol. 2024; 22(5):e3002519.

PMID: 38787858 PMC: 11156437. DOI: 10.1371/journal.pbio.3002519.


Male harm suppresses female fitness, affecting the dynamics of adaptation and evolutionary rescue.

Gomez-Llano M, Faria G, Garcia-Roa R, Noble D, Carazo P Evol Lett. 2024; 8(1):149-160.

PMID: 38370549 PMC: 10871930. DOI: 10.1093/evlett/qrac002.


Effects of past mating behavior versus past ejaculation on male mate choice and male attractiveness.

Chung M, Head M, Fox R, Jennions M Behav Ecol. 2024; 35(2):arae002.

PMID: 38273897 PMC: 10807976. DOI: 10.1093/beheco/arae002.


Separating the effects of paternal age and mating history: Evidence for sex-specific paternal effect in eastern mosquitofish.

Aich U, Chowdhury S, Jennions M Evolution. 2022; 76(7):1565-1577.

PMID: 35544673 PMC: 9543789. DOI: 10.1111/evo.14498.


References
1.
Kirkwood T, Rose M . Evolution of senescence: late survival sacrificed for reproduction. Philos Trans R Soc Lond B Biol Sci. 1991; 332(1262):15-24. DOI: 10.1098/rstb.1991.0028. View

2.
Miller L, Brooks R . The effects of genotype, age, and social environment on male ornamentation, mating behavior, and attractiveness. Evolution. 2006; 59(11):2414-25. View

3.
Van Voorhies W . Production of sperm reduces nematode lifespan. Nature. 1992; 360(6403):456-8. DOI: 10.1038/360456a0. View

4.
Rahman M, Gasparini C, Turchini G, Evans J . Experimental reduction in dietary omega-3 polyunsaturated fatty acids depresses sperm competitiveness. Biol Lett. 2014; 10(9). PMC: 4190967. DOI: 10.1098/rsbl.2014.0623. View

5.
Simmons L, Roberts B . Bacterial immunity traded for sperm viability in male crickets. Science. 2005; 309(5743):2031. DOI: 10.1126/science.1114500. View