Evaluation of honey bee larvae data: sensitivity to PPPs and impact analysis of EFSA bee GD.

J. Lückmann, R. Becker, M. Miles, A. Alix, A. Dinter, Stefan Kroder, E. Pilling, N. Ruddle, Christof W. Schneider, Amanda E. Sharples, Laurent Oger
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引用次数: 1

Abstract

In addition to other assessments, the EFSA bee guidance document (2013) requires the risk assessment of plant protection products on honey bee larvae. At the time the EFSA GD was finalized, no data on honey bee larvae were available due to absence of suitable methods. That is why in 2013 the European Crop Protection Association (ECPA) perfomed an impact analysis of the new EFSA risk assessment, using extrapolated endpoints derived from acute oral honey bee endpoints. Today, a number of honey bee larvae toxicity studies (138 active substances or formulated products) have been conducted according to the newly developed testing methods for single exposure (OECD TG 237) repeated exposure studies until the end of the larval development (D7/D8) and repeated exposure testing (OECD GD 239) until adult hatch (D22). These experimental data have been used to determine the ‘pass rates’ for 215 worst case uses (72 fungicide spray and solid uses, 91 herbicide spray uses, incl. 8 PGR uses and in total 52 insecticide spray and solid uses, incl. 2 nematicide and 3 IGR uses) according to the EFSA Bee GD and to compare with the original ECPA impact analysis. As standardized test methods for non- Apis bees larvae were not available, risk assessment according to EFSA for bumblebees and solitary bees based on the honey bee endpoint as surrogate corrected by a safety factor of 10. Morevoer, the sensitivity of the NOEDs at D8 and D22 in repeated exposure (D 22) studies were analysed. Overall, the toxicity of fungicides and herbicides to honey bee larvae (expressed as means and medians of NOED and LD50 values) was moderate to low, while insecticides as expected displayed stronger toxicity. Moreover, the endpoints for herbicides were on average a factor of 2 higher than fungicides which ranges within the normal biological variability (factor of 3). In addition, it is unclear, if the difference is related to a slightly higher toxicity or other factors like different physical chemical properties (e.g. lower solubility). For insecticides, toxicity was about 125 (based on medians) and 6 to 8 (based on means) times higher than herbicides. In the screening risk assessment according to EFSA Bee GD the majority of fungicide (83.3%) and herbicide (95.6%) uses passed the risk assessment for larvae; whereas, for all insecticide uses thr pass rate was about 29%. In the Tier 1 risk assessment, these pass rates slightly increased and were even higher in the ‘treated crop’ and ‘weed in the field’ scenarios for fungicide and herbicide uses, almost being 100%. Pass rates for insecticide uses did not improve very much and amounted to be about 42% for both scenarios. When basing the risk assessment of bumblebee and solitary bee larvae on 1/10th of the honey bee larval endpoint, the majority of active substances and their respective products will fail the screening (overall about 96%) and Tier 1 risk assessment (overall about 90%). Alternative risk assessment approaches proposed by ECPA (e.g. following the EPPO approach; ECPA Option 1 using refinement options and more representative assumptions) or comparing an assummed exposure concentration to the NOEC (ECPA Option 2) led to a slight increase (Option 1) or even no differences in the pass rates (Option 2a) compared to EFSA Tier 1 risk assessment. Thus both, the standard risk assessment according to the EFSA Bee GD as well as the alternative ECPA Option 1 and 2 result in a clear distinction between products with high toxicity (insecticides) vs. non-toxic products (herbicides and fungicides) for the honey bee risk assessment. The sensitivity analysis of repeated exposure studies according OECD GD 239 indicated that in most cases toxicity did not increase during the pupation period between D8 and D22. Thus, the larval growing period between D3 and D8 represents the most sensitive period of the pre-imaginal development.
蜜蜂幼虫数据的评估:对购买力平价的敏感性和EFSA蜜蜂GD的影响分析。
除其他评估外,欧洲食品安全局蜜蜂指导文件(2013年)还要求对蜜蜂幼虫的植物保护产品进行风险评估。在EFSA GD最终确定时,由于缺乏合适的方法,没有关于蜜蜂幼虫的数据。这就是为什么欧洲作物保护协会(ECPA)在2013年对新的欧洲食品安全局风险评估进行了影响分析,使用了从蜜蜂急性口服终点推断的终点。目前,已经根据新开发的单次暴露测试方法(OECD TG 237)进行了许多蜜蜂幼虫毒性研究(138种活性物质或配方产品),重复暴露研究直到幼虫发育结束(D7/D8)和重复暴露测试(OECD GD 239)直到成虫孵化(D22)。根据EFSA Bee GD,这些实验数据已用于确定215种最坏情况使用的“通过率”(72种杀菌剂喷雾和固体使用,91种除草剂喷雾使用,包括8种PGR使用,总共52种杀虫剂喷雾和固体用途,包括2种杀线虫剂和3种IGR使用),并与最初的ECPA影响分析进行比较。由于没有针对非Apis蜜蜂幼虫的标准化测试方法,根据EFSA,基于蜜蜂终点作为替代品的大黄蜂和独居蜜蜂的风险评估通过10的安全系数进行了校正。此外,还分析了重复暴露(D22)研究中D8和D22处NOED的敏感性。总体而言,杀菌剂和除草剂对蜜蜂幼虫的毒性(以NOED和LD50值的平均值和中位数表示)为中等至较低,而杀虫剂的毒性如预期的那样更强。此外,除草剂的终点平均比在正常生物变异范围内的杀菌剂高出2倍(3倍)。此外,尚不清楚这种差异是否与略高的毒性或其他因素有关,如不同的物理化学性质(如较低的溶解度)。杀虫剂的毒性约为125倍(基于中位数),是除草剂的6-8倍(基于平均值)。在根据EFSA Bee GD进行的筛选风险评估中,大多数杀菌剂(83.3%)和除草剂(95.6%)的使用通过了幼虫的风险评估;而对于所有杀虫剂的使用,thr通过率约为29%。在一级风险评估中,这些通过率略有上升,在杀菌剂和除草剂使用的“处理过的作物”和“田间杂草”情况下甚至更高,几乎为100%。杀虫剂使用的通过率没有太大改善,两种情况下的通过率都约为42%。当根据蜜蜂幼虫终点的1/10对大黄蜂和独居蜜蜂幼虫进行风险评估时,大多数活性物质及其各自的产品将无法通过筛查(总体约96%)和一级风险评估(总体约90%)。ECPA提出的替代风险评估方法(例如,遵循EPPO方法;ECPA选项1使用改进选项和更具代表性的假设)或将假定的暴露浓度与NOEC进行比较(ECPA选项2)导致与EFSA一级风险评估相比,通过率略有增加(选项1),甚至没有差异(选项2a)。因此,根据EFSA Bee GD的标准风险评估以及ECPA备选方案1和2,在蜜蜂风险评估中,可以明确区分高毒性产品(杀虫剂)和无毒产品(除草剂和杀菌剂)。根据OECD GD 239对重复暴露研究的敏感性分析表明,在大多数情况下,D8和D22之间的化蛹期毒性没有增加。因此,D3和D8之间的幼虫生长期代表了想象前发育的最敏感时期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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