BASF Corporation, Raleigh, North Carolina, USA.
Pollinator Research Task Force (PRTF), USA.
Integr Environ Assess Manag. 2024 Nov;20(6):2283-2293. doi: 10.1002/ieam.4982. Epub 2024 Aug 7.
The assessment of pesticide risks to bees in North America currently relies in part on Tier 1 honey bee laboratory toxicity studies to support the registration and registration review processes for crop protection chemicals. For immature stages, the studies follow two standardized test designs recommended by the Organization for Economic Cooperation (OECD), evaluating acute (seven-day single-dose, TG OECD 237) and chronic (22-day repeated-dose, GD OECD 239) toxicity in bee larvae. In this article, we aim to evaluate the current approach for generating and interpreting honey bee larval toxicity data, enhancing pesticide risk assessment for pollinators. First, by considering that the repeated-dose larval study covers all stages of honey bee brood development up to adult emergence, we compared endpoints (larval LD/ED50 and LC/EC50 values) from seven-day acute exposure studies with the 22-day chronic exposure studies. Our goal was to identify the study design offering greater sensitivity in assessing pesticide toxicity to immature bees. Our second objective involved analyzing available weight data from emerged adults and comparing it to survival endpoints (e.g., NOEL and LD50) to determine if the weight after adult emergence would accurately represent a sensitive indicator of pesticide effects on developing honey bees. Our analysis determined that the use of a single 22-day chronic exposure study adequately covers all immature stages and that the toxicity values based on cumulative dose are more accurate and representative measures of exposure for immature bees than using endpoints based on estimated daily doses. Furthermore, our analysis suggests that measuring the weight of emerged adults was a more sensitive indicator than mortality of treatment-related effects in 22% of the compounds included in our analysis. Here we also discuss the importance of standardized protocols for proper collection of weight after emergence and the need for further discussion on the relevance of this parameter at risk assessment scheme. Integr Environ Assess Manag 2024;20:2283-2293. © 2024 Pollinator Research Task Force. Integrated Environmental Assessment and Management published by Wiley Periodicals LLC on behalf of Society of Environmental Toxicology & Chemistry (SETAC).
目前,北美的蜜蜂农药风险评估部分依赖于 1 级蜜蜂实验室毒性研究,以支持作物保护化学品的注册和注册审查过程。对于幼虫期,研究遵循经济合作与发展组织 (OECD) 推荐的两种标准化测试设计,评估蜜蜂幼虫的急性(七天单次剂量,TG OECD 237)和慢性(22 天重复剂量,GD OECD 239)毒性。在本文中,我们旨在评估当前生成和解释蜜蜂幼虫毒性数据的方法,以增强传粉媒介的农药风险评估。首先,考虑到重复剂量幼虫研究涵盖了蜜蜂幼虫发育到成虫的所有阶段,我们比较了七天急性暴露研究与 22 天慢性暴露研究的终点(幼虫 LD/ED50 和 LC/EC50 值)。我们的目标是确定在评估农药对不成熟蜜蜂的毒性方面更敏感的研究设计。我们的第二个目标是分析可用的成虫体重数据,并将其与生存终点(例如,NOEL 和 LD50)进行比较,以确定成虫后体重是否能准确代表对发育中的蜜蜂的农药影响的敏感指标。我们的分析确定,单一的 22 天慢性暴露研究足以涵盖所有幼虫期,基于累积剂量的毒性值比基于估计日剂量的终点更准确和代表性地反映了对不成熟蜜蜂的暴露。此外,我们的分析表明,在我们分析的化合物中有 22%的情况下,测量成虫的体重比处理相关效应的死亡率更能作为敏感指标。在这里,我们还讨论了标准化协议对正确收集成虫后体重的重要性,以及在风险评估方案中进一步讨论该参数相关性的必要性。Integr Environ Assess Manag 2024;20:2283-2293。 © 2024 传粉媒介研究任务组。综合环境评估与管理由 Wiley Periodicals LLC 代表环境毒理学与化学学会(SETAC)出版。