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Updated: Apr 16, 2026

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Published on: July 22, 2025
The maintenance of single-locus polymorphism by maternal selection
Hamish G Spencer1, Kai X Chiew2
1Allan Wilson Centre, Department of Zoology, University of Otago, Dunedin 9054, New Zealand hamish.spencer@otago.ac.nz.
Maternal selection may preserve genetic variation but is less likely to maintain many alleles compared to standard models. This variation, however, resists genetic drift and shows heterozygous advantage.
Area of Science:
- Population genetics
- Evolutionary biology
- Quantitative genetics
Background:
- Natural selection's role in maintaining genetic variation is a key question in population genetics.
- Standing variation in natural populations presents a challenge for evolutionary theory.
- Maternal selection, where fitness depends on both the individual and its mother's genotype, offers a different selective framework.
Purpose of the Study:
- To investigate the polymorphism-maintaining properties of maternal selection.
- To compare maternal selection with standard viability selection models.
- To understand how mutation and selection jointly shape genetic diversity under maternal selection.
Main Methods:
- Utilizing a mathematical model proposed by Gavrilets.
- Employing a "parameter-space" approach to estimate the proportion of conditions preserving allelic variation.
- Using a "constructionist" approach to study polymorphism development over time.
Main Results:
- Maternal selection increases the parameter-state space for multiallelic polymorphism compared to constant viability selection.
- Despite a larger parameter space, maternal selection is less effective at maintaining a high number of alleles.
- Variation maintained by maternal selection exhibits heterozygous advantage and resilience to genetic drift.
Conclusions:
- Maternal selection can maintain genetic variation, but may favor fewer alleles than expected.
- The genetic diversity maintained under maternal selection is robust against genetic drift.
- Population mean fitness may temporarily decline following new mutations but tends to recover.
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