Bumblebee colony development following chronic exposure to field-realistic levels of the neonicotinoid pesticide thiamethoxam under laboratory conditions


Neonicotinoid pesticides are used in agriculture to reduce damage from crop pests. However, beneficial insects such as bees can come into contact with these pesticides when foraging in treated areas, with potential consequences for bee declines and pollination service delivery. Honeybees are typically used as a model organism to investigate insecticide impacts on bees, but relatively little is known about impacts on other taxa such as bumblebees. In this experiment, we chronically exposed whole mature bumblebee (Bombus terrestris) colonies to field-realistic levels of the neonicotinoid thiamethoxam (2.4ppb & 10ppb) over four weeks, and compared colony growth under laboratory conditions. We found no impact of insecticide exposure on colony weight gain, or the number or mass of sexuals produced, although colonies exposed to 2.4ppb produced larger males. As previous studies have reported pesticide effects on bumblebee colony growth, this may suggest that impacts on bumblebee colonies are more pronounced for colonies at an earlier stage in the reproductive cycle. Alternatively, it may also indicate that thiamethoxam differs in toxicity compared to previously tested neonicotinoids in terms of reproductive effects. In either case, assessing bumblebee colony development under field conditions is likely more informative for real world scenarios than tests conducted in laboratory conditions.


Bumblebees are important pollinators in temperate regions, providing essential pollination services to both crops and wild plants1,2,3. However, concern over the decline of bumblebee pollinators4,5,6,7,8,9,10 has resulted in recent interest in the potential role of pesticide exposure as one of the factors driving these declines. Bumblebees foraging in agricultural environments are likely to encounter a range of pesticides applied to crops as sprays, soil drenches or seed treatments. The dramatic rise in use of systemic neonicotinoid seed treatments, now the world’s most widely used class of insecticides11, raise particular concerns as the pesticide active ingredients are translocated into all tissues of the treated crop, including the nectar and pollen that can be collected and consumed by bees12,13,14. In addition, as neonicotinoid insecticides are also found in soils15 and water courses16, 17, it is perhaps unsurprising that residues have also been detected in wild flowering plants18,19,20,21,22. Therefore, there are multiple possible routes of exposure for bumblebees to these insecticides over extended periods of time, resulting in chronic exposure. These levels of exposure in the field are typically below levels that cause direct mortality in bees, but can cause a range of sub lethal effects23,24,25.

However, while risk assessments for pesticide registration and usage are currently carried out using honeybees as the only model for insect pollinators24,25,26,27, impacts on bumblebees and other taxa can be different28,29,30,31,32. In the last few years, a greater number of studies reporting impacts of exposure to neonicotinoid insecticides on bumblebees have been published, most of which have investigated the effects of imidacloprid26. Indeed, exposure to field-realistic levels of imidacloprid have been shown to affect bumblebee foraging33, 34, colony growth and reproduction34,35,36,37. Imidacloprid use is declining, and other neonicotinoids (e.g. thiamethoxam and clothianidin) are being used widely as seed treatments for oilseed rape (canola), maize (corn), soy and other crops worldwide11, 16, 38. In comparison to imidacloprid, less is known about the impacts of exposure to thiamethoxam and clothianidin on bumblebees (but see refs 26, 31, 3948).

The aim of our experiment was to investigate potential impacts of thiamethoxam on bumblebee (Bombus terrestris) colony growth in a laboratory setting. We exposed bumblebee colonies chronically to low, field-realistic levels of thiamethoxam in sugar water solutions for a period of up to 27 days, to mimic exposure through nectar while foraging on treated crops such as oilseed rape (Brassica napus). Eight established colonies were exposed to an untreated sucrose solution (control treatment) and eight colonies each were exposed to a sucrose solution containing either 2.4ppb and 10ppb thiamethoxam respectively. After a further 13–14 days we counted the numbers of workers and sexuals produced, and estimated the average weight of individuals and total biomass of each caste per colony.


On average, colonies gained 336 g in weight over the course of the experiment, and produced 389 workers (range 146–606) and 261 males (range 132–397; see Table S1). Males were on average bigger than workers (mean dry mass: males 0.09 g, workers 0.05 g). Seven of 24 colonies produced queens (2 colonies each from control and 10ppb treatments, and 3 from the 2.4ppb treatment group), and numbers of queens produced ranged from two to 34 per colony. There were no differences in colony weight among treatments at the start of the experiment (F2,21 = 0.014, p = 0.99) or the number of individuals they contained (F2,21 = 1.74, p = 0.2; Table 1). However, colony weight did not correlate with the numbers of individuals in each colony (Pearsons product moment correlation; t = 1.3, df = 22, p = 0.22).

Table 1 Means (±standard error) of the variables measured per Bombus terrestris colony. N = eight colonies per treatment (24 colonies in total).

Exposure to pesticide did not influence the weight gained by colonies over the course of the experiment (F2,21 = 0.99, p = 0.39; Fig. 1), or the numbers of workers (F2,21 = 0.095, p = 0.9), males (F2,21 = 1.02, p = 0.38) or queens (KW test, χ2 = 1.14, df = 2, p = 0.57; Table 1; Fig. 2) produced. Although there was also no impact of treatment on weight of individual workers (F2,21 = 0.92, p = 0.41) or queens (F2,21 = 0.12, p = 0.89), there was a significant effect on the weight of males (F2,21 = 4.47, p = 0.02); males were significantly larger in colonies exposed to 2.4ppb pesticide than both controls and those exposed to 10ppb thiamethoxam (Table 1; Fig. S1). However, there was no effect of treatment on total biomass of any castes produced (workers: F2,21 = 0.73, p = 0.50, males: F2,21 = 0.03, p = 0.97, queens: F2,21 = 2.23, p = 0.13; Table 1; Fig. S2).

Figure 1

Bombus terrestris colony weight gain (g, including weight of outer box) over course of experiment from day 1 (2/4/2014) – day 40 (13/5/2014). N = eight colonies per treatment (24 colonies in total). Each colony was exposed to its respective treatment for a period of 26–27 days.

Figure 2

The mean number of workers, males and queens produced per Bombus terrestris colony, with colonies exposed to control, 2.4ppb thiamethoxam and 10ppb thiamethoxam. N = eight colonies per treatment (24 colonies in total), and error bars show standard error. No significant difference was found between any of the treatments in all three measures.


Our work shows that mature bumblebee colonies exposed chronically to field-realistic levels of thiamethoxam in a laboratory setting develop in a similar way to control colonies, with little impact of pesticide on colony growth or sexual production. The only measure that differed among treatment groups was the production of males; we found that colonies exposed to 2.4ppb thiamethoxam produced fewer males, but that the males produced were heavier than those from control or 10ppb thiamethoxam colonies. Taken together these patterns resulted in no differences across treatments in overall biomass of males produced. This suggests that colonies exposed to 2.4ppb thiamethoxam might differentially allocate resources, investing more resources into each male, but producing fewer overall. Although the difference was not significant, more colonies exposed to 2.4ppb pesticide produced queens (3 rather than 2) in this study, which could also be linked to differential investment by pesticide exposed colonies. However, as we found no significant impacts on other variables measured, there are unlikely to be strong implications for colony reproduction. Our work adds to the increasing body of research assessing the impacts of pesticide exposure on bumblebees.

Laboratory tests

In this study we found no impacts of thiamethoxam exposure on bumblebee colony development under laboratory conditions. This is similar to findings reported by Laycock et al.40, who also observed no impacts of thiamethoxam at 16ppb or less on bumblebee feeding or fecundity in micro-colonies under laboratory conditions. However, other laboratory studies have found different patterns; for example Elston et al.46 reported reduced reproductive effort in bumblebee micro-colonies exposed to 10ppb thiamethoxam, and Fauser-Misslin et al.39 observed that exposure to pollen and nectar treated with 4ppb thiamethoxam and 1.5ppb clothianidin significantly reduced the reproductive success of whole colonies. Experimental colonies in our study were relatively large at the onset of pesticide exposure (containing an average of 99 workers), and it is likely that most of the workers, and some of the males, were already larvae or even pupae when pesticide exposure began. The colonies used in previous studies in which impacts of thiamethoxam on reproduction were found were exposed at an early stage of the colony cycle when, on average, only 1039 or 6046 workers were present. This suggests that pesticide effects may be more apparent at earlier stages of the colony cycle34, when individuals are also exposed to pesticide during larval development (when pollen consumption is much greater) and not only as adults. Oilseed rape (canola), one of the major flowering crops attractive to bees that is treated systemically with neonicotinoid pesticides, typically flowers in early summer when bumblebee colonies are likely to be at the start of development49. Although we did not find any impacts of treatment on colony weight (as a proxy for total colony size including brood), we did not specifically measure brood effects as colonies were large which prevented non-destructive counts of number of brood cells. Therefore, more work on the effects of pesticide exposure on a variety of colony developmental stages would be useful, as the severity of impacts on growth and reproduction are likely to be related to colony size at the time of exposure.

Laboratory versus field studies

Our study was carried out in a laboratory setting, where bumblebees were fed nectar and pollen inside the nest box and, therefore, did not have to work hard to forage or provision their colonies. Under field and semi-field conditions, bumblebees are faced with more challenging environments and need to forage (at least partially) for their own food from real flowers. As exposure to both imidacloprid33, 50 or thiamethoxam42,43,44,45 can affect bumblebee learning and foraging ability, it is unsurprising that effects on colony development are likely to be more severe under field conditions. A second point is that in the field bumblebees are also exposed to variable amounts of mixtures of pesticides in the nectar and pollen of crops and wild plants18, 21, 51. Although it is hard to replicate this level or variability in the lab setting, it is important to understand the effects of consistent amounts of single pesticides before examining variability. Therefore, we would suggest running field studies in conjunction with laboratory-based experiments when investigating pesticide impacts on bumblebee reproduction to ensure results are representative of the wider environment.

Impacts of different neonicotinoids

Impacts of thiamethoxam exposure on colony development under laboratory conditions are variable, but reported impacts of imidacloprid on bumblebee colony development and reproduction at field realistic levels are more consistent, with dose-dependent reductions in fecundity in micro-colonies36 and reduced colony development of entire colonies52. In semi-field studies, although thiamethoxam exposure led to changes in foraging patterns and reduced pollen collection, impacts on development in a small number of colonies were not recorded44, and even an increase in colony weight has been reported (although this study lacks appropriate replication53). On the other hand, colonies exposed to imidacloprid showed changes in foraging patterns and reduced pollen collection, and subsequent deficits in colony development34, colony growth37 and queen production35. With two experiments using a similar setup, bumblebee micro-colonies exposed to imidacloprid in the lab showed a dose-dependent decline in fecundity, starting at field-realistic levels, which was attributed to reduced feeding on both syrup and pollen36, but no effects on feeding or micro-colony development at field-realistic levels of thiamethoxam exposure40. Studies investigating clothianidin impacts have found: 1) fewer adult workers and sexuals produced in colonies exposed to 5ppb clothianidin41, 2) reduced growth and reproduction in bumblebee colonies placed beside clothianidin treated oilseed rape fields in a fully replicated field experiment31 and 3) no effect on bumblebee reproduction (although this study lacked appropriate replication54). Moffat et al.55 found compound specific effects of different neonicotinoids on different variables; for example, exposure to 2.5ppb imidacloprid and thiamethoxam (but not clothianidin) decreased colony strength, whereas increased queen production was only found in colonies treated with clothianidin. Together, these studies support the view that exposure to various neonicotinoids result in differential impacts for bumblebees. However, the majority of these comparisons are circumstantial, and more work is needed to directly compare the effects of different neonicotinoid types on bumblebees using common methodological approaches and exposure levels.


One of the major concerns about the impacts of pesticides on bees is that the pollination services they deliver may be affected. Although we find no impacts of thiamethoxam on the growth of mature bumblebee colonies in this study, previous work has found impacts on queen reproductive development48 and ability to found colonies47, and that worker bees exposed to thiamethoxam show reduced learning ability, reduced pollen collection, and differential visitation of flowers42, 45. Therefore, although thiamethoxam may not cause impacts on colonies under laboratory conditions, it could have different impacts in a field setting where the ability to forage and collect pollen are critical for normal colony development56, and where bees are often exposed to multiple pesticides simultaneously21. Bees with impaired learning and/or pollen collecting ability are unlikely to be delivering the same level of pollination services to crops and wild plants. Therefore, although impacts on colony development may not be evident, pollination service delivery could be affected by changes in individual behaviour related to thiamethoxam exposure rather than via impacts at the colony level.

Our work shows that chronic exposure to a neonicotinoid pesticide in a laboratory setting has little impact on the growth of mature bumblebee colonies. A comparison of our work with other published studies leads us to make a number of suggestions for future research directions and pesticide testing. Firstly, pesticide effects should be examined at multiple stages of the colony cycle to ensure any differences between effects on mature and developing colonies are understood47, 48, 57, as they may not be similar. Secondly, pesticide testing should be carried out under both laboratory and field conditions, because bees under field conditions may be more susceptible to pesticide effects than those in the laboratory. Lastly, there is a need to directly compare different neonicotinoid pesticides, using common methodologies, as effects of thiamethoxam may be different to other neonicotinoids (e.g. imidacloprid).

Materials and Methods

Insecticide solutions of 2.4 and 10ppb thiamethoxam used in subsequent experimental procedures were prepared as follows: an initial stock solution was created by dissolving 100 mg thiamethoxam (PESTANAL, Analytical Standard, Sigma Aldrich) in 100 ml acetone (1 mg/ml). We then added 10 µg or 2.4 µg of this solution to a litre of 40% sucrose, to create solutions of 10ppb and 2.4ppb thiamethoxam, respectively (these concentrations are calculated on a volume/ volume (v/v) basis; on a weight/ weight (w/w) basis solutions would be 2ppb and 8.5ppb, respectively). These concentrations were chosen as field-realistic; the lower concentration (2.4ppb) was measured in nectar pots of bumblebee colonies foraging in agricultural areas in the UK12 and in pollen collected by honeybees in France38, while the higher concentration (10ppb) is within the range that has been measured in the nectar and pollen of a variety of treated crops and wild plants19, 58, 59, and appreciably below the mean levels found in pollen collected by bumblebees in UK rural areas21. We also made a control solution by repeating the process outlined above but using an aliquot of 10ppb acetone only (i.e. no pesticide).

Twenty-four Bombus terrestris audax colonies were obtained from Biobest (Westerlo, Belgium) at the start of April 2014, each containing a queen and an average of 99 workers (range 57–133). On arrival, colonies were weighed to estimate overall colony size (without either the sucrose feeder reservoir and outer cardboard box), and then assigned sequentially to one of three treatment groups (10ppb thiamethoxam, 2.4ppb thiamethoxam and control) based on decreasing mass (but randomly assigned within block). Each day, three colonies (one from each treatment) began treatment, until after 7 days all colonies were receiving their respective sucrose solutions (eight control colonies, eight colonies exposed to 2.4ppb thiamethoxam, and eight colonies exposed to 10ppb thiamethoxam). Each colony was exposed to its respective treatment for a period of 26–27 days, and all sucrose solutions were actively consumed. Colonies were weighed weekly over the entire study period, to estimate colony growth. All colonies were given a large gravity feeder containing their treated solution each day, and were fed equal amounts of untreated, defrosted, honeybee-collected pollen.

After 26–27 days of exposure to their respective treatments, treatment of colonies stopped. All colonies were then fed untreated sucrose until 13th May (40 days since colonies had arrived from the supplier), when all colonies were frozen at −20 °C. Subsequently, colonies were dissected and the numbers of workers, males and queens (gynes) produced were counted. Thirty workers, 30 males, and all queens were dried in a drying oven at 60 °C for 3 days, and then weighed to give the dry mass of each individual. This information was used to a) calculate an average dry mass (weight) of individuals of each caste in each colony, and b) to estimate the total dry mass of each caste produced60.

We tested for differences in weight gain, average dry mass of individuals of each caste (workers, males and queens), and total biomass of each caste using analysis of variance. Differences in the numbers of males and workers produced were tested using generalized linear models with Poisson distribution specified for counts, and a Kruskal-Wallis test for numbers of queens produced as data were non-normally distributed. All models were verified by inspecting distribution of residuals, and all analyses were carried out in the stats package in R v 3.1.1061.

Data availability statement

All data are available in the supplementary information


  1. 1.

    Corbet, S. A., Williams, I. H. & Osborne, J. L. Bees and the pollination of crops and wild flowers in the European community. Bee World 72, 47–59 (1991).

    Article  Google Scholar 

  2. 2.

    Button, L. & Elle, E. Wild bumble bees reduce pollination deficits in a crop mostly visited by managed honey bees. Agriculture, Ecosystems & Environment 197, 255–263 (2014).

    Article  Google Scholar 

  3. 3.

    Kleijn, D. et al. Delivery of crop pollination services is an insufficient argument for wild pollinator conservation. Nature Communications 6, 7414 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  4. 4.

    Williams, P. H. & Osborne, J. L. Bumblebee vulnerability and conservation world-wide. Apidologie 40, 367–387 (2009).

    Article  Google Scholar 

  5. 5.

    Grixti, J. C., Wong, L. T., Cameron, S. A. & Favret, C. Decline of bumble bees (Bombus) in the North American Midwest. Biological Conservation 142, 75–84 (2009).

    Article  Google Scholar 

  6. 6.

    Dupont, Y. L., Damgaard, C. & Simonsen, V. Quantitative historical change in bumblebee (Bombus spp.) assemblages of red clover fields. PLoS One 6, e25172 (2011).

    CAS  Article  PubMed  PubMed Central  ADS  Google Scholar 

  7. 7.

    Bommarco, R., Lundin, O., Smith, H. G. & Rundlöf, M. Drastic historic shifts in bumble-bee community composition in Sweden. Proceedings of the Royal Society B: Biological Sciences 279, 309–315 (2011).

    Google Scholar 

  8. 8.

    Cameron, S. A. et al. Patterns of widespread decline in North American bumble bees. PNAS 108, 662–667 (2011).

    CAS  Article  PubMed  PubMed Central  ADS  Google Scholar 

  9. 9.

    Williams, P. Environmental change and the distributions of British bumble bees (Bombus Latr.). Bee World 67, 50–61 (1986).

    Article  Google Scholar 

  10. 10.

    Williams, P. H. The distribution and decline of British Bumble Bees (Bombus Latr.). Journal of Apicultural Research 21, 236–245 (1982).

    Article  Google Scholar 

  11. 11.

    Goulson, D. An overview of the environmental risks posed by neonicotinoid insecticides. Journal of Applied Ecology 50, 977–987 (2013).

    Article  Google Scholar 

  12. 12.

    Thompson, H. et al. Effects of neonicotinoid seed treatments on bumble bee colonies under field conditions. York, UK, Food and Environment Research Agency, 2013.

  13. 13.

    Pohorecka, K. et al. Residues of neonicotinoid insecticides in bee collected plant materials from oilseed rape crops and their effect on bee colonies. Journal of Apicultural Science 56, 115–132 (2012).

    Article  Google Scholar 

  14. 14.

    Cutler, G. C. & Scott-Dupree, C. D. A field study examining the effects of exposure to neonicotinoid seed-treated corn on commercial bumble bee colonies. Ecotoxicology 23, 1755–1763 (2014).

    Article  Google Scholar 

  15. 15.

    Jones, A., Harrington, P. & Turnbull, G. Neonicotinoid concentrations in arable soils after seed treatment applications in preceding years. Pest Management Science 70, 1780–1784 (2014).

    CAS  Article  PubMed  Google Scholar 

  16. 16.

    Hladik, M. L., Kolpin, D. W. & Kuivila, K. M. Widespread occurrence of neonicotinoid insecticides in streams in a high corn and soybean producing region, USA Environmental Pollution 193, 189–196 (2014).

    CAS  Article  PubMed  Google Scholar 

  17. 17.

    Samson-Robert, O., Labrie, G., Chagnon, M. & Fournier, V. Neonicotinoid-contaminated puddles of water represent a risk of intoxication for honey bees. PLoS One 9, e108443 (2014).

    Article  PubMed  PubMed Central  ADS  Google Scholar 

  18. 18.

    Krupke, C. H., Hunt, G. J., Eitzer, B. D., Andino, G. & Given, K. Multiple routes of pesticide exposure for honey bees living near agricultural fields. PLoS One 7, e29268 (2012).

    CAS  Article  PubMed  PubMed Central  ADS  Google Scholar 

  19. 19.

    Stewart, S. D. et al. Potential exposure of pollinators to neonicotinoid insecticides from the use of insecticide seed treatments in the mid-southern United States. Environmental Science & Technology 48, 9762–9769 (2014).

    CAS  Article  ADS  Google Scholar 

  20. 20.

    Botías, C. et al. Neonicotinoid residues in wildflowers, a potential route of chronic exposure for bees. Environmental Science & Technology 49, 12731–12740 (2015).

    Article  ADS  Google Scholar 

  21. 21.

    David, A. et al. Widespread contamination of wildflower and bee-collected pollen with complex mixtures of neonicotinoids and fungicides commonly applied to crops. Environment International 88, 169–178 (2016).

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Long, E. Y. & Krupke, C. H. Non-cultivated plants present a season-long route of pesticide exposure for honey bees. Nature Communications 7, 11629 (2016).

    CAS  Article  PubMed  PubMed Central  ADS  Google Scholar 

  23. 23.

    Desneux, N., Decourtye, A. & Delpuech, J.-M. The sublethal effects of pesticides on beneficial arthropods. Annual Review of Entomology 52, 81–106 (2007).

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Godfray, H. C. J. et al. A restatement of the natural science evidence base concerning neonicotinoid insecticides and insect pollinators. Proceedings of the Royal Society B: Biological Sciences 281, 20140558 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Godfray, H. C. J. et al. A restatement of recent advances in the natural science evidence base concerning neonicotinoid insecticides and insect pollinators. Proceedings of the Royal Society B: Biological Sciences 282, 20151821 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  26. 26.

    Lundin, O., Rundlöf, M., Smith, H. G., Fries, I. & Bommarco, R. Neonicotinoid insecticides and their impacts on bees: a systematic review of research approaches and identification of knowledge gaps. PLoS One 10, e0136928 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Cabrera, A. R. et al. Initial recommendations for higher-tier risk assessment protocols for bumble bees, Bombus spp. (Hymenoptera: Apidae). Integrated Environmental Assessment and Management 12, 222–229 (2016).

    Article  PubMed  Google Scholar 

  28. 28.

    Arena, M. & Sgolastra, F. A meta-analysis comparing the sensitivity of bees to pesticides. Ecotoxicology 23, 324–334 (2014).

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    Cresswell, J. E. et al. Differential sensitivity of honey bees and bumble bees to a dietary insecticide (imidacloprid). Zoology 115, 365–371 (2012).

    Article  PubMed  Google Scholar 

  30. 30.

    Piiroinen, S. & Goulson, D. Chronic neonicotinoid pesticide exposure and parasite stress differentially affects learning in honeybees and bumblebees. Proceedings of the Royal Society B: Biological Sciences 283, 20160246 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  31. 31.

    Rundlöf, M. et al. Seed coating with a neonicotinoid insecticide negatively affects wild bees. Nature 521, 77–80 (2015).

    Article  PubMed  ADS  Google Scholar 

  32. 32.

    Woodcock, B. A. et al. Country-specific effects of neonicotinoid pesticides on honey bees and wild bees. Science 356, 1393–1395 (2017).

    CAS  Article  PubMed  Google Scholar 

  33. 33.

    Feltham, H., Park, K. & Goulson, D. Field realistic doses of pesticide imidacloprid reduce bumblebee pollen foraging efficiency. Ecotoxicology 23, 317–323 (2014).

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Gill, R. J., Ramos-Rodriguez, O. & Raine, N. E. Combined pesticide exposure severely affects individual- and colony-level traits in bees. Nature 491, 105–108 (2012).

    CAS  Article  PubMed  PubMed Central  ADS  Google Scholar 

  35. 35.

    Whitehorn, P. R., O’Connor, S., Wackers, F. L. & Goulson, D. Neonicotinoid pesticide reduces bumble bee colony growth and queen production. Science 336, 351–352 (2012).

    CAS  Article  PubMed  ADS  Google Scholar 

  36. 36.

    Laycock, I., Lenthall, K. M., Barratt, A. T. & Cresswell, J. E. Effects of imidacloprid, a neonicotinoid pesticide, on reproduction in worker bumble bees (Bombus terrestris). Ecotoxicology 21, 1937–1945 (2012).

    CAS  Article  PubMed  Google Scholar 

  37. 37.

    Moffat, C. et al. Chronic exposure to neonicotinoids increases neuronal vulnerability to mitochondrial dysfunction in the bumblebee (Bombus terrestris). The FASEB Journal 29, 2112–2119 (2015).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  38. 38.

    Pilling, E., Campbell, P., Coulson, M., Ruddle, N. & Tornier, I. A four-year field program investigating long-term effects of repeated exposure of honey bee colonies to flowering crops treated with thiamethoxam. PLoS One 8, e77193 (2013).

    CAS  Article  PubMed  PubMed Central  ADS  Google Scholar 

  39. 39.

    Fauser-Misslin, A., Sadd, B., Neumann, P. & Sandrock, C. Influence of combined pesticide and parasite exposure on bumblebee colony traits in the laboratory. Journal of Applied Ecology 51, 450–459 (2014).

    Article  Google Scholar 

  40. 40.

    Laycock, I., Cotterell, K. C., O’Shea-Wheller, T. A. & Cresswell, J. E. Effects of the neonicotinoid pesticide thiamethoxam at field-realistic levels on microcolonies of Bombus terrestris worker bumble bees. Ecotoxicology and Environmental Safety 100, 153–158 (2014).

    CAS  Article  PubMed  Google Scholar 

  41. 41.

    Arce, A. N. et al. Impact of controlled neonicotinoid exposure on bumblebees in a realistic field setting. Journal of Applied Ecology online early, doi:10.1111/1365-2664.12792 (2016).

  42. 42.

    Stanley, D. A. et al. Neonicotinoid pesticide exposure impairs crop pollination services provided by bumblebees. Nature 528, 548–550 (2015).

    CAS  Article  PubMed  PubMed Central  ADS  Google Scholar 

  43. 43.

    Stanley, D. A. & Raine, N. E. Chronic exposure to a neonicotinoid pesticide alters the interactions between bumblebees and wild plants. Functional Ecology 30, 1132–1139 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  44. 44.

    Stanley, D. A., Russell, A. L., Morrison, S. J., Rogers, C. & Raine, N. E. Investigating the impacts of field-realistic exposure to a neonicotinoid pesticide on bumblebee foraging, homing ability and colony growth. Journal of Applied Ecology 53, 1440–1449 (2016).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  45. 45.

    Stanley, D. A., Smith, K. E. & Raine, N. E. Bumblebee learning and memory is impaired by chronic exposure to a neonicotinoid pesticide. Scientific Reports 5, 16508 (2015).

    CAS  Article  PubMed  PubMed Central  ADS  Google Scholar 

  46. 46.

    Elston, C., Thompson, H. & Walters, K. A. Sub-lethal effects of thiamethoxam, a neonicotinoid pesticide, and propiconazole, a DMI fungicide, on colony initiation in bumblebee (Bombus terrestris) micro-colonies. Apidologie 44, 563–574 (2013).

    CAS  Article  Google Scholar 

  47. 47.

    Baron, G. L., Jansen, V. A. A., Brown, M. J. F., & Raine, N. E. Pesticide reduces bumblebee colony establishment and increases probability of population extinction. Nature Ecology & Evolution (2017 in press).

  48. 48.

    Baron, G. L., Raine, N. E. & Brown, M. J. F. General and species-specific impacts of a neonicotinoid insecticide on the ovary development and feeding of wild bumblebee queens. Proceedings of the Royal Society B: Biological Sciences 284 (2017).

  49. 49.

    Stanley, D. A., Gunning, D. & Stout, J. C. Pollinators and pollination of oilseed rape crops (Brassica napus L.) in Ireland: ecological and economic incentives for pollinator conservation. Journal of Insect Conservation 17, 1181–1189 (2013).

    Article  Google Scholar 

  50. 50.

    Gill, R. J. & Raine, N. E. Chronic impairment of bumblebee natural foraging behaviour induced by sublethal pesticide exposure. Functional Ecology 28, 1459–1471 (2014).

    Article  Google Scholar 

  51. 51.

    Botías, C., David, A., Hill, E. M. & Goulson, D. Quantifying exposure of wild bumblebees to mixtures of agrochemicals in agricultural and urban landscapes. Environmental Pollution 222, 73–82 (2017).

    Article  PubMed  Google Scholar 

  52. 52.

    Bryden, J., Gill, R. J., Mitton, R. A. A., Raine, N. E. & Jansen, V. A. A. Chronic sublethal stress causes bee colony failure. Ecology Letters 16, 1463–1469 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  53. 53.

    Thompson, H. et al. Monitoring the effects of thiamethoxam applied as a seed treatment to winter oilseed rape on the development of bumblebee (Bombus terrestris) colonies. Pest Management Science 72, 1737–1742 (2016).

    CAS  Article  PubMed  ADS  Google Scholar 

  54. 54.

    Sterk, G., Peters, B., Gao, Z. & Zumkier, U. Large-scale monitoring of effects of clothianidin-dressed OSR seeds on pollinating insects in Northern Germany: effects on large earth bumble bees (Bombus terrestris). Ecotoxicology 25, 1666–1678 (2016).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  55. 55.

    Moffat, C. et al. Neonicotinoids target distinct nicotinic acetylcholinase receptors and neurons, leading to differential risks to bumblebees. Scientific Reports 6, 24764 (2016).

    Article  PubMed  PubMed Central  ADS  Google Scholar 

  56. 56.

    Pelletier, L. & McNeil, J. N. The effect of food supplementation on reproductive success in bumblebee field colonies. Oikos 103, 688–694 (2003).

    Article  Google Scholar 

  57. 57.

    Fauser, A., Sandrock, C., Neumann, P. & Sadd, B. Neonicotinoids override a parasite exposure impact onhibernation success of a key bumblebee pollinator. Ecological Entomology 42, 306–314 (2017).

    Article  Google Scholar 

  58. 58.

    Dively, G. P. & Kamel, A. Insecticide residues in pollen and nectar of a cucurbit crop and their potential exposure to pollinators. Journal of Agricultural and Food Chemistry 60, 4449–4456 (2012).

    CAS  Article  PubMed  Google Scholar 

  59. 59.

    Castle, S. J., Byrne, F. J., Bi, J. L. & Toscano, N. C. Spatial and temporal distribution of imidacloprid and thiamethoxam in citrus and impact on Homalodisca coagulata populations. Pest Management Science 61, 75–84 (2005).

    CAS  Article  PubMed  Google Scholar 

  60. 60.

    Baron, G. L., Raine, N. E. & Brown, M. J. F. Impact of chronic exposure to a pyrethroid pesticide on bumblebees and interactions with a trypanosome parasite. Journal of Applied Ecology 51, 460–469 (2014).

    CAS  Article  Google Scholar 

  61. 61.

    R: A language and environment for statistical computing. (R Foundation for Statistical Computing, Vienna, Austria. http://www.R-project.org, 2014).

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This study was supported by UK Insect Pollinators Initiative grant BB/I000178/1 funded jointly by the Living with Environmental Change programme, Biotechnology and Biological Sciences Research Council (BBSRC), Wellcome Trust, Scottish Government, Department for Environment, Food and Rural Affairs (Defra) and Natural Environment Research Council (NERC). NER is supported as the Rebanks Family Chair in Pollinator Conservation by The W. Garfield Weston Foundation. We thank anonymous reviewers whose comments helped to improve this manuscript.

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D.A.S. and N.E.R. conceived the project, designed the experiment and wrote the manuscript. D.A.S. carried-out the experiment and performed statistical analyses.

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Correspondence to Dara A. Stanley.

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Stanley, D.A., Raine, N.E. Bumblebee colony development following chronic exposure to field-realistic levels of the neonicotinoid pesticide thiamethoxam under laboratory conditions. Sci Rep 7, 8005 (2017). https://doi.org/10.1038/s41598-017-08752-x

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