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Assessing the population relevance of endocrine‐disrupting effects for nontarget vertebrates exposed to plant protection products
Author(s) -
Crane Mark,
Hallmark Nina,
Lagadic Laurent,
Ott Katharina,
Pickford Dan,
Preuss Thomas,
Thompson Helen,
Thorbek Pernille,
Weltje Lennart,
Wheeler James R
Publication year - 2019
Publication title -
integrated environmental assessment and management
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.665
H-Index - 57
eISSN - 1551-3793
pISSN - 1551-3777
DOI - 10.1002/ieam.4113
Subject(s) - population , adverse effect , adverse outcome pathway , hazard , risk analysis (engineering) , environmental health , biology , environmental resource management , business , ecology , medicine , environmental science , pharmacology , computational biology
The European Commission intends to protect vertebrate wildlife populations by regulating plant protection product (PPP) active substances that have endocrine‐disrupting properties with a hazard‐based approach. In this paper we consider how the Commission's hazard‐based regulation and accompanying guidance can be operationalized to ensure that a technically robust process is used to distinguish between substances with adverse population‐level effects and those for which it can be demonstrated that adverse effects observed (typically in the laboratory) do not translate into adverse effects at the population level. Our approach is to use population models within the adverse outcome pathway framework to link the nonlinear relationship between adverse effects at the individual and population levels in the following way: (1) use specific protection goals for focal wildlife populations within an ecosystem services framework; (2) model the effects of changes in population‐related inputs on focal species populations with individual‐based population models to determine thresholds between negligible and nonnegligible (i.e., adverse) population‐level effects; (3) compare these thresholds with the relevant endpoints from laboratory toxicity tests to determine whether they are likely to be exceeded at hazard‐based limits or the maximum tolerated dose/concentration from the experimental studies. If the population threshold is not exceeded, then the substance should not be classified as an endocrine disruptor with population‐relevant adversity unless there are other lines of evidence within a weight‐of‐evidence approach to challenge this. We believe this approach is scientifically robust and still addresses the political and legal requirement for a hazard‐based assessment. Integr Environ Assess Manag 2019;15:278–291. © 2018 The Authors. Integrated Environmental Assessment and Management published by Wiley Periodicals, Inc. on behalf of Society of Environmental Toxicology & Chemistry (SETAC)