Intralocus Sexual Conflict Unresolved by Sex-Limited Trait Expression

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Intralocus Sexual Conflict Unresolved by Sex-Limited Trait Expression Tomohiro Harano, Kensuke Okada, Satoshi Nakayama, Takahisa Miyatake, David J. Hosken  Current Biology  Volume 20, Issue 22, Pages 2036-2039 (November 2010) DOI: 10.1016/j.cub.2010.10.023 Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 1 The Substantial Sexual Dimorphism Seen in Beetle Mandible Size Left image shows the male head with enlarged mandibles; right image shows a female's head where the mandible exaggeration is completely lacking. Mandibles are used in male-male competition, and males with larger mandibles have higher fitness. Current Biology 2010 20, 2036-2039DOI: (10.1016/j.cub.2010.10.023) Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 2 Female Fitness Female fitness measured as lifetime fecundity (LRS: mean ± SE) in the experimental populations (L = populations with artificial selection for larger male mandible size; C = control populations where there was no artificial selection imposed on male mandible size; S = populations with artificial selection for smaller male mandible size). There was a significant effect of selection (treatment) on LRS (general linear model [GLM] of treatment [L,C,S] effects using population means: F2,3 = 22.2; p = 0.014; post hoc tests [Fisher's PLSD] revealed that L < C < S [all p < 0.04]). Current Biology 2010 20, 2036-2039DOI: (10.1016/j.cub.2010.10.023) Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 3 Female Trait Evolution Characters that potentially provide a proximate explanation for the differences in female LRS across the experimental populations (L = populations with artificial selection for larger male mandible size; C = control populations where there was no artificial selection imposed on male mandible size; S = populations with artificial selection for smaller male mandible size). Separate GLMs were used to assess each variable with selection (treatment: L,C,S) as a fixed effect. (A) Female longevity (weeks). (B) Egg volume (mm3 × 10−3). (C) Female body mass (mg). (D) Posterior mass (mesothorax, metathorax, and abdomen; mg). Only the size of the female rear portion (posterior mass, D) significantly differed across treatments, and this difference remains statistically significant with sequential Bonferroni correction (F2,3 = 213.6; p < 0.001; post hoc tests [Fisher's PLSD] show that L < C < S [all p < 0.002]). None of the other characters measured significantly differed across treatments (all F < 1.8; all p > 0.30). Note that the posterior mass differences precisely mirror the fitness differences (Figure 2). Data are means ± SE. Current Biology 2010 20, 2036-2039DOI: (10.1016/j.cub.2010.10.023) Copyright © 2010 Elsevier Ltd Terms and Conditions