Abstract

The existence of widespread male same-sex sexual behaviour (SSB) is puzzling: why does evolution allow costly homosexual activity to exist, when reproductive fitness is primarily achieved through heterosexual matings? Here, we used experimental evolution to understand why SSB occurs in the flour beetle Tribolium castaneum. By varying the adult operational sex ratio across 82–106 generations, we created divergent evolutionary regimes that selected for or against SSB depending upon its function. Male-biased (90:10 M:F) regimes generated strong selection on males from intrasexual competition, and demanded improved ability to locate and identify female mates. By contrast, Female-biased regimes (10:90 M:F) generated weak male–male competition, and relaxed selection on mate-searching abilities in males. If male SSB functions through sexually selected male–male competition, it should be more evident within Male-biased regimes, where reproductive competition is nine times greater, than in the Female-biased regimes. By contrast, if SSB exists due to inaccurate mate choice, it should be reduced in Male-biased regimes, where males experience stronger selection for improved mate finding and discrimination abilities than in the Female-biased regime, where most potential mating targets are female. Following these divergent evolutionary regimes, we measured male engagement in SSB through choice experiments simultaneously presenting female and male mating targets. Males from both regimes showed similar overall levels of mating activity. However, there were significant differences in levels of SSB between the two regimes: males that evolved through male-biased operational sex ratios located, mounted and mated more frequently with the female targets. By contrast, males from female-biased selection histories mated less frequently with females, exhibiting almost random choice between male and female targets in their first mating attempt. Following experimental evolution, we therefore conclude that SSB does not function through sexually selected male–male competition, but instead occurs because males fail to perfectly discriminate females as mates.

Highlights

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  • Male-biased regime males engaged in 4.3 ± 0.2 mountings within each 15 min trial, and Female-biased males engaged in 4.4 ± 0.2 mountings (c23,283 1⁄4 0.1, P 1⁄4 0.780; Fig. 2a)

  • Following experimental evolution under divergent intensities of sexual selection our study reveals that male sex sexual behaviour (SSB) in T. castaneum is the consequence of inaccurate mate discrimination, where males are targeted for mating instead of females

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Summary

METHODS

Tribolium castaneum demonstrates significant levels of SSB (Levan et al, 2009; Martin, Kruse, & Switzer, 2015; Spratt, 1980), is readily cultured in the laboratory under experimental control, freely engages in measurable mating behaviour, and can be reared from egg to adult in 1 month (Sokoloff, 1972). Experimental evolution was applied by altering the adult operational sex ratio at every generation to create either Male- or Female-biased conditions for reproduction, as described previously in detail (Michalczyk et al, 2011b; Lumley et al, 2015). Mounting and mating time investment Despite similar total time invested by focal males from either experimental evolution regime in mounting and mating (Fig. 2), focal males from the Male-biased background spent 12% more of their mounting time targeting the female, with 68% of their total time spent mounting females (and 32% investing in SSB on males). Female-biased regime focal males spent 56% of their time mounting female targets (and 44% engaging in SSB with males; c23,283 1⁄4 5.7, P 1⁄4 0.017; Fig. 4c). 35% engaging in SSB with male targets (c23,211 1⁄4 12.6, P < 0.001; Fig. 4d)

RESULTS
Findings
Declaration of Interest
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