Abstract
Understanding the effects of neonicotinoid insecticides on bees is vital because of reported declines in bee diversity and distribution1,2,3 and the crucial role bees have as pollinators in ecosystems and agriculture4. Neonicotinoids are suspected to pose an unacceptable risk to bees, partly because of their systemic uptake in plants5, and the European Union has therefore introduced a moratorium on three neonicotinoids as seed coatings in flowering crops that attract bees6. The moratorium has been criticized for being based on weak evidence7, particularly because effects have mostly been measured on bees that have been artificially fed neonicotinoids8,9,10,11. Thus, the key question is how neonicotinoids influence bees, and wild bees in particular, in real-world agricultural landscapes11,12,13. Here we show that a commonly used insecticide seed coating in a flowering crop can have serious consequences for wild bees. In a study with replicated and matched landscapes, we found that seed coating with Elado, an insecticide containing a combination of the neonicotinoid clothianidin and the non-systemic pyrethroid β-cyfluthrin, applied to oilseed rape seeds, reduced wild bee density, solitary bee nesting, and bumblebee colony growth and reproduction under field conditions. Hence, such insecticidal use can pose a substantial risk to wild bees in agricultural landscapes, and the contribution of pesticides to the global decline of wild bees1,2,3 may have been underestimated. The lack of a significant response in honeybee colonies suggests that reported pesticide effects on honeybees cannot always be extrapolated to wild bees.
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Acknowledgements
We thank the farmers for collaboration, the project group for feedback, A. Gunnarson for farmer contacts and seeds, M. Ahlström Olsson and Lindesro AB for bumblebee colonies, A. Andersson and C. Du Rietz for examining bumblebee colonies, B. Andréasson, T. Carling and A. Andersson for producing and assessing honeybee colonies, J. Kreuger for discussions on pesticide quantification, and M. Stjernman for extracting land use information. Funding was provided by the Swedish Civil Contingencies Agency to R.B., I.F., T.R.P. and H.G.S., by the Carl Tryggers Foundation for Scientific Research, the Royal Physiographic Society, and the Swedish Research Council (330-2014-6439) to M.R, and by Formas to H.G.S. and R.B.
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R.B., I.F., T.R.P. and H.G.S. conceived the project. M.R. designed the study, coordinated the work, analysed the data, and prepared the manuscript. G.K.S.A., V.H., L.H., B.K.K. and J.Y. collected the data. O.J. quantified the pesticide residues. All authors contributed to the interpretation of results and writing of the manuscript.
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Extended data figures and tables
Extended Data Figure 1 O. bicornis emergence and B. terrestris colonies.
a, Mean (± 95% confidence limits) proportion emergence of O. bicornis from cocoons in relation to treatment (control or insecticide seed coating), with higher emergence for males than females (generalized linear mixed model, binomial error distribution, logit link; F1, 14 = 14.97, P = 0.0017), no difference between treatments (F1, 7 = 0.71, P = 0.43) and no interaction (F1, 14 = 0.01, P = 0.94). n = 8 fields per treatment, with 12 female and 15 male cocoons at each field. Photos (with permission; Morgan Boch): left, emerged O. bicornis cocoon; right, O. bicornis female at a trap nests filled with cardboard nest tubes. b, Mean (± 95% confidence limits) weight of B. terrestris colonies at placement at the fields in relation to treatment (linear mixed model, F1, 7 = 0.99, P = 0.35). n = 8 fields per treatment, with six colonies at each field. Photos (M.R.): left, B. terrestris worker foraging in the oilseed rape; right, house containing three B. terrestris colonies. Means and confidence limits in panels a and b are based on back-transformed, model-estimated least square means. c, B. terrestris silk cocoon width distribution of all cocoons in four colonies (two from two different control fields and two from two different fields with insecticide seed treatment) initially examined to separate between queen and worker/male cocoons. Dashed vertical line indicates selected cut-off width at 12 mm (the lowest value between the two peaks), with queens larger (or equal) and workers/males smaller. Photo (M.R.): B. terrestris colony under examination.
Extended Data Figure 2 Power curves for honeybee colony strength.
a, b, Relationship between power and effect size estimated for the honeybee model (Extended Data Table 6), with effect size expressed as the difference in honeybee colony strength (number of bees per colony) (a) and the percentage change in colony strength (b) between colonies at control fields and at fields with insecticide seed coating after placement at the oilseed rape fields. Grey reference lines indicate a power of 0.8 and the corresponding effect size.
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Rundlöf, M., Andersson, G., Bommarco, R. et al. Seed coating with a neonicotinoid insecticide negatively affects wild bees. Nature 521, 77–80 (2015). https://doi.org/10.1038/nature14420
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DOI: https://doi.org/10.1038/nature14420
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