Female plasticity tends to reduce sexual conflict

被引:12
作者
McLeod, David V. [1 ]
Day, Troy [1 ]
机构
[1] Queens Univ, Dept Math & Stat, 99 Univ Ave, Kingston, ON K7L 3N6, Canada
来源
NATURE ECOLOGY & EVOLUTION | 2017年 / 1卷 / 03期
基金
加拿大自然科学与工程研究理事会;
关键词
DROSOPHILA-MELANOGASTER; EVOLUTION; MALES; ADAPTATION; SELECTION; FITNESS; PEPTIDE; COST;
D O I
10.1038/s41559-016-0054
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Sexual conflict is the divergence of evolutionary interests between the sexes. A neglected aspect of sexual conflict theory is that the conflict often occurs within the female's body, which can lead to a power asymmetry between the sexes. In particular, the female may often be able to respond flexibly to the actions of the male, and so exhibits plasticity. Here, we consider the implications of female plasticity, and find that it tends to result in lower levels of sexual conflict. We then relate our results to a comparison of pre-versus post-copulatory sexual conflict, and we also show that this asymmetry between males and females reduces the likelihood of runaway selection, preventing co-evolutionary arms races. Finally, we discuss our results in the context of the evolution of adaptive harm and sexual conflict when there are direct benefits.
引用
收藏
页数:4
相关论文
共 50 条
  • [1] Quantifying variation in female internal genitalia: no evidence for plasticity in response to sexual conflict risk in a seed beetle
    Wyber, Blake W.
    Dougherty, Liam R.
    McNamara, Kathryn
    Mehnert, Andrew
    Shaw, Jeremy
    Tomkins, Joseph L.
    Simmons, Leigh W.
    PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2021, 288 (1954)
  • [2] Sexual conflict drives male manipulation of female postmating responses in Drosophila melanogaster
    Hollis, Brian
    Koppik, Mareike
    Wensing, Kristina U.
    Ruhmann, Hanna
    Genzoni, Eleonore
    Erkosar, Berra
    Kawecki, Tadeusz J.
    Fricke, Claudia
    Keller, Laurent
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 116 (17) : 8437 - 8444
  • [3] Sexual Conflict: Male Control of Female Longevity
    Zwoinska, Martyna
    Lind, Martin I.
    Maklakov, Alexei A.
    CURRENT BIOLOGY, 2014, 24 (05) : R196 - R198
  • [4] Resource-dependent evolution of female resistance responses to sexual conflict
    Rostant, Wayne G.
    Mason, Janet S.
    de Coriolis, Jean-Charles
    Chapman, Tracey
    EVOLUTION LETTERS, 2020, 4 (01) : 54 - 64
  • [5] Contrasting effects of intralocus sexual conflict on sexually antagonistic coevolution
    Pennell, Tanya M.
    de Haas, Freek J. H.
    Morrow, Edward H.
    van Doorn, G. Sander
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (08) : E978 - E986
  • [6] Sexual selection, phenotypic plasticity and female reproductive output
    Fox, Rebecca J.
    Fromhage, Lutz
    Jennions, Michael D.
    PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2019, 374 (1768)
  • [7] Sexual conflict and ecology: Species composition and male density interact to reduce male mating harassment and increase female survival
    Gomez-Llano, Miguel A.
    Bensch, Hanna M.
    Svensson, Erik I.
    EVOLUTION, 2018, 72 (04) : 906 - 915
  • [8] Release from intralocus sexual conflict? Evolved loss of a male sexual trait demasculinizes female gene expression
    Rayner, Jack G.
    Pascoal, Sonia
    Bailey, Nathan W.
    PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2019, 286 (1901)
  • [9] Evolution of female choice under intralocus sexual conflict and genotype-by-environment interactions
    Li, Xiang-Yi
    Holman, Luke
    PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2018, 373 (1757)
  • [10] Spatial structure imposes sex-specific costs but does not reduce interlocus sexual conflict
    Halder, Subhasish
    Kar, Shramana
    Sethi, Simran
    Tewari, Swadha
    Verma, Tanya
    Nandy, Bodhisatta
    BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, 2024,