ArticleBMC ecology and evolution2021
Fine-scale habitat heterogeneity favours the coexistence of supergene-controlled social forms in Formica selysi.
Article in BMC ecology and evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- Biased social chromosome transmission in males of the fire ant Solenopsis invicta.G3 (Bethesda, Md.) · 2025Article
- Spatial structure could explain the maintenance of alternative reproductive tactics in tree cricket males.Biology open · 2024Article
- A supergene-controlling social structure in Alpine ants also affects the dispersal ability and fecundity of each sex.Proceedings. Biological sciences · 2024Article
- Ecological strategies of (pl)ants: Towards a world-wide worker economic spectrum for ants.Functional ecology · 2023Article
- Iterative evolution of supergene-based social polymorphism in ants.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022Review
- Unbalanced selection: the challenge of maintaining a social polymorphism when a supergene is selfish.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022Article
- Effects of social organization and elevation on spatial genetic structure in a montane ant.Ecology and evolution · 2022Article
- A novel distribution of supergene genotypes is present in the socially polymorphic ant Formica neoclara.BMC ecology and evolution · 2022Article
- Disentangling the mechanisms linking dispersal and sociality in supergene-mediated ant social forms.Proceedings. Biological sciences · 2021Article
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5 authors.
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No grant is acknowledged in the PubMed record.
Abstract
backgroundSocial insects vary widely in social organization, yet the genetical and ecological factors influencing this variation remain poorly known. In particular, whether spatially varying selection influences the maintenance of social polymorphisms in ants has been rarely investigated. To fill this gap, we examined whether fine-scale habitat heterogeneity contributes to the co-existence of alternative forms of social organization within populations. Single-queen colonies (monogyne social form) are generally associated with better colonization abilities, whereas multiple-queen colonies (polygyne social form) are predicted to be better competitors and monopolize saturated habitats. We hypothesize that each social form colonizes and thrives in distinct local habitats, as a result of their alternative dispersal and colony founding strategies. Here, we test this hypothesis in the Alpine silver ant, in which a supergene controls polymorphic social organization.
resultsMonogyne and polygyne colonies predominate in distinct habitats of the same population. The analysis of 59 sampling plots distributed across six habitats revealed that single-queen colonies mostly occupy unconnected habitats that were most likely reached by flight. This includes young habitats isolated by water and old habitats isolated by vegetation. In contrast, multiple-queen colonies were abundant in young, continuous and saturated habitats. Hence, alternative social forms colonize and monopolize distinct niches at a very local scale.
conclusionsAlternative social forms colonized and monopolized different local habitats, in accordance with differences in colonization and competition abilities. The monogyne social form displays a colonizer phenotype, by efficiently occupying empty habitats, while the polygyne social form exhibits a competitor phenotype, thriving in saturated habitats. The combination of the two phenotypes, coupled with fine-scale habitat heterogeneity, may allow the coexistence of alternative social forms within populations. Overall, these results suggest that spatially varying selection may be one of the mechanisms contributing to the maintenance of genetic polymorphisms in social organization.
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