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Biology subjects

Treanore, E. D.

Publications and source records attributed to Treanore, E. D..

3 recordsLinked to original sources

Contrasting life history strategies explain contrasting phenology of two co-occurring bumble bee species

Across species, changing environmental conditions are altering major phenological milestones. In seasonal environments, this can involve shifts in the timing of activity onset, growth, reproduction, and senescence; however, predicting these responses can be challenging and often requires species-specific information. In this study, we investigated phenological patterns of bumble bee colony development using observations from wild nests of two common species, Bombus griseocollis and B. impatiens. Using observations of nest traffic, we documented dates of nest-searching, peak worker activity, first gyne (new queen) production, and colony senescence over three years of field data collection. We also tested whether colony growth was density dependent, because longstanding life history models have shown that colony growth patterns determine the optimal timing of reproduction in constant environments. Here, we present a novel extension of these models, using them to infer that density-independent colony growth should be associated with extended phenology in warmer years, while density-dependent should have consistent phenology. In total, we found 79 wild nests, including 34 reproductive colonies (19 B. griseocolis and 15 B. impatiens). Bombus impatiens colonies were larger, had a longer activity period, and showed density-independent growth and later reproduction in warmer years, while B. griseocollis colonies were smaller, shorter-lived, and showed density-dependent growth and similar dates of reproduction across years. Both species had higher gyne production in warmer years. These results highlight the role of life history theory for predicting interspecific variation in phenological changes, as well as a research framework for exploring possible evolutionary mismatches of existing life histories in changing environments.

ecology↗

Built to change: dominance strategy changes with life stage in a primitively eusocial bee

Access to reproduction is determined by an individual dominances rank in many species and is achieved through aggression and/or dominance signalling. In eusocial insects one or several dominant females (queens) monopolize reproduction but to what extent queens rely on aggression and signalling remains obscure. Aggression is costly and its efficiency depends on the group size, whereas signalling may reduce the risks and costs of aggression. Both strategies are used to regulate reproduction in social taxa, with aggression being more common in small social groups, compared to signalling in larger societies. Here, we examine the use of aggression and chemical signalling in a social species (Bombus impatiens) where the dominant queen interacts with increasing numbers of workers as she ages. We found that the queens strategy to monopolize reproduction changes with life stage, shifting from overt aggression to chemical signalling as the queen gets older. Particularly, old queens exhibited a higher ratio of short to long cuticular hydrocarbons compared to young queens, an endogenous shift that was attributed to age, as all egg-laying queens were fecund and kept with the same number of workers. Our findings contribute to the understanding of reproductive dominance in the context of an individuals life history.

evolutionary biology↗

The role of insect diapause in the divergence of social female castes: Insights from primitively eusocial bumble bee workers

Insects maximize their fitness by exhibiting predictable and adaptive seasonal patterns in response to changing environmental conditions. These seasonal patterns are often expressed even when insects are kept in captivity, suggesting they are functionally and evolutionary important. In this study we examined whether workers of the eusocial bumble bee Bombus impatiens maintained a seasonal signature when kept in captivity. We used an integrative approach and compared worker egg-laying, ovarian activation, body size and mass, lipid content in the fat body, cold tolerance and expression of genes related to cold tolerance, metabolism, and stress throughout colony development. We found that bumble bee worker physiology and gene expression patterns shift from reproductive-like to diapause-like as the colony ages. Workers eclosing early in the colony cycle had increased egg-laying and ovarian activation, and reduced cold tolerance, body size, mass, and lipid content in the fat body, in line with a reproductive-like profile, while late-eclosing workers exhibited the opposite characteristics. Furthermore, expression patterns of genes associated with reproduction and diapause differed between early- and late-eclosing workers, partially following the physiological patterns. We suggest that a seasonal signature, innate to individual workers, the queen or the colony is used by workers as a social cue determining the phenology of the colony and discuss possible implications for understanding reproductive division of labor in bumble bee colonies and the evolutionary divergence of female castes in the genus Bombus.

evolutionary biology↗