Abstract

The honey bee, Apis mellifera L. (Hymenoptera: Apidae), is a model organism for pollinators in risk assessment frameworks globally. The acute toxicity tests with adult honey bees for contact and oral exposure are part of the requirements for pesticide registration and are typically conducted with the active ingredient. A question often asked is if the typical end-use product (TEP) is more toxic than the technical grade active ingredient (TGAI) to honey bees. We explored this question by mining publicly available databases from regulatory agencies worldwide, where testing with the TEP is required. The objective of this study was to determine whether TEPs are comparable in toxicity to the TGAI. The dataset was analyzed via a 3 × 3 contingency table with toxicity categories, as the data cannot be computed for regression analysis. Of the 151 active ingredients with reported endpoints for contact exposure, 28 were classified as either moderately or highly toxic, 123 were classified as practically nontoxic, and 3 were inconclusive. Only two (1.3%) were reclassified from nontoxic to moderately toxic as the TEP. Of the 141 active ingredients with reported endpoints for oral exposure, 23 were classified as moderately or highly toxic, 113 were classified as practically nontoxic, and 5 were inconclusive. Only five (3.6%) were reclassified from nontoxic to moderately toxic as the TEP. Fewer than 5% of the total TEPs evaluated (contact and oral) were shown to be more toxic than the TGAI, suggesting that the risk assessments of TGAIs would be sufficiently protective to pollinators at the screening laboratory level.

Highlights

  • The honey bee, Apis mellifera L. (Hymenoptera: Apidae), serves as a model organism for pollinators in the current risk assessment framework in North America and other regions of the world (EFSA 2013, USEPA, PMRA, and CDPR 2014, USEPA 2016)

  • Acute toxicity endpoints are the medial lethal doses (LD50) and are expressed as μg active ingredient/bee. These tests are required and typically conducted with the technical grade active ingredient (TGAI), in some cases, a typical end-use product (TEP; formulated product) may be needed in addition to data on TGAI if there are data indicating that a TEP is potentially more toxic than the TGAI, and bees may be directly exposed to the intact TEP (USEPA, PMRA, and CDPR 2014)

  • We identified cases where the toxicity classification of the TEPs was different compared to the TGAI

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Summary

Introduction

The honey bee, Apis mellifera L. (Hymenoptera: Apidae), serves as a model organism for pollinators in the current risk assessment framework in North America and other regions of the world (EFSA 2013, USEPA, PMRA, and CDPR 2014, USEPA 2016). The acute toxicity tests with adult honey bees for contact and oral exposure are part of the current requirements for pesticide registration. Acute toxicity endpoints are the medial lethal doses (LD50) and are expressed as μg active ingredient/bee. These tests are required and typically conducted with the technical grade active ingredient (TGAI), in some cases, a typical end-use product (TEP; formulated product) may be needed in addition to data on TGAI if there are data indicating that a TEP is potentially more toxic than the TGAI, and bees may be directly exposed to the intact TEP (USEPA, PMRA, and CDPR 2014). Sometimes the TEP is used to overcome solubility limits with the TGAI in the bee testing diet (sucrose solution) for the oral acute test

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