ArticlePloS one2022
Male survivorship and the evolution of eusociality in partially bivoltine sweat bees.
Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- The eusocial non-code: Unveiling the impact of noncoding RNAs on Hymenoptera eusocial evolution.Non-coding RNA research · 2025Review
- Reply to da Silva: Helping behavior can emerge without its prior adaptive evolution.Proceedings of the National Academy of Sciences of the United States of America · 2024Article
- Variation in season length and development time is sufficient to drive the emergence and coexistence of social and solitary behavioural strategies.Proceedings. Biological sciences · 2024Article
- Maternal manipulation of offspring size can trigger the evolution of eusociality in promiscuous species.Proceedings of the National Academy of Sciences of the United States of America · 2024Article
- Variation in season length and development time is sufficient to drive the emergence and coexistence of social and solitary behavioral strategies.bioRxiv : the preprint server for biology · 2024Article
- Genetic differentiation at extreme latitudes in the socially plastic sweat bee Halictus rubicundus.PloS one · 2024Article
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Authors and funding
2 authors.
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Abstract
Eusociality, where workers typically forfeit their own reproduction to assist their mothers in raising siblings, is a fundamental paradox in evolutionary biology. By sacrificing personal reproduction, helpers pay a significant cost, which must be outweighed by indirect fitness benefits of helping to raise siblings. In 1983, Jon Seger developed a model showing how in the haplodiploid Hymenoptera (ants, wasps and bees), a partially bivoltine life cycle with alternating sex ratios may have promoted the evolution of eusociality. Seger predicted that eusociality would be more likely to evolve in hymenopterans where a foundress produces a male-biased first brood sex ratio and a female-biased second brood. This allows first brood females to capitalize on super-sister relatedness through helping to produce the female-biased second brood. In Seger's model, the key factor driving alternating sex ratios was that first brood males survive to mate with females of both the second and the first brood, reducing the reproductive value of second brood males. Despite being potentially critical in the evolution of eusociality, however, male survivorship has received little empirical attention. Here, we tested whether first brood males survive across broods in the facultatively eusocial sweat bee Halictus rubicundus. We obtained high estimates of survival and, while recapture rates were low, at least 10% of first brood males survived until the second brood. We provide empirical evidence supporting Seger's model. Further work, measuring brood sex ratios and comparing abilities of first and second brood males to compete for fertilizations, is required to fully parameterize the model.
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