Abstract
The 10 fatty acid ester components of brood pheromone were extracted from larvae of different populations of USA and South African honey bees and subjected to gas chromatography-mass spectrometry quantitative analysis. Extractable amounts of brood pheromone were not significantly different by larval population; however, differences in the proportions of components enabled us to classify larval population of 77% of samples correctly by discriminant analysis. Honeybee releaser and primer pheromone responses to USA,Africanized and–European pheromone blends were tested. Texas-Africanized and Georgia-European colonies responded with a significantly greater ratio of returning pollen foragers when treated with a blend from the same population than from a different population. There was a significant interaction of pheromone blend by adult population source among Georgia-European bees for modulation of sucrose response threshold, a primer response. Brood pheromone blend variation interacted with population for pollen foraging response of colonies, suggesting a self recognition cue for this pheromone releaser behavior. An interaction of pheromone blend and population for priming sucrose response thresholds among workers within the first week of adult life suggested a more complex interplay of genotype, ontogeny, and pheromone blend.
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Abbreviations
- BP:
-
brood pheromone
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Acknowledgements
For editorial notes and field assistance, the authors are indebted to Vincent Dietemann. The authors also thank Christian Pirk, GW Burlin, Art Cavazos, Lizette Peters, Ramesh Sagili, and Howard Williams for technical support and assistance. This study was funded by grants from the USDA-NRI 2004-35302-15031 and the Texas Honey Bee Legislative Initiative.
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Metz, B.N., Pankiw, T., Tichy, S.E. et al. Variation in and Responses to Brood Pheromone of the Honey Bee (APIS mellifera L.). J Chem Ecol 36, 432–440 (2010). https://doi.org/10.1007/s10886-010-9775-5
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DOI: https://doi.org/10.1007/s10886-010-9775-5