Male mating choices: The drive behind menopause?
Anthia Le1, Kristen Hawkes2, Peter S Kim3
1School of Mathematics and Physics, The University of Queensland, Brisbane, Australia.
Theoretical Population Biology
|May 7, 2022
Summary
Human females evolved menopause because ancestral males preferred younger mates. However, this study
Area of Science:
- Evolutionary biology
- Human evolution
- Reproductive science
Background:
- Humans exhibit greater longevity and a distinct postmenopausal stage compared to other great apes.
- The evolutionary drivers of human menopause, or old-age infertility in females, remain a subject of scientific inquiry.
- Previous research proposed male mating preferences for younger females as a key factor in menopause evolution.
Purpose of the Study:
- To re-evaluate the hypothesis that ancestral male mating choices drove the evolution of menopause.
- To investigate the robustness of the male-mate-choice hypothesis using a mathematical modeling approach.
- To explore the conditions under which male preference for younger mates could lead to female infertility.
Main Methods:
- Development of an ordinary differential equations (ODEs) model analogous to a prior agent-based model (ABM).
- Replication of key findings from Morton et al. (2013) using the ODE system.
- Extensive sensitivity analysis across various parameters and initial conditions to test hypothesis robustness.
Main Results:
- The ODE model confirmed the qualitative conclusions of the original ABM under specific conditions.
- Sensitivity analysis revealed that even minor deviations from exclusive mating preference for young females counteract menopause evolution.
- The study challenges the sufficiency of the male-mate-choice hypothesis alone.
Conclusions:
- The male-mate-choice hypothesis, as proposed, is likely incomplete in explaining the evolution of menopause.
- Further explanations are needed for the evolutionary stability of an exclusive male mating strategy with young females.
- Additional factors beyond male preference are likely involved in the evolution of human female post-reproductive lifespan.
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