监管科学实践的潜在削减--微塑料案例

Johanna Kramm
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引用次数: 0

摘要

在过去的几十年里,出现了一个与微塑料有关的新研究领域,该领域在微塑料造成的风险方面仍然面临着高度的不确定性和相互冲突的观点。迄今为止,社会研究尚未涉及评估微塑料风险所需的监管科学实践以及相关的伦理问题。因此,本文旨在分析核心监管科学实践的作用,即与微塑料有关的风险评估。我借鉴凯伦-巴拉德(Karen Barad)的研究成果,将这些监管科学实践概念化为划定边界的实践,从而产生代理切割。我将说明,科学和监管的划界实践产生的代理切割决定了微塑料的特性以及对人类和环境健康产生 "真正 "后果的监管行动。我的经验案例表明,存在着不同版本的风险评估--一种以阈值为基础,另一种以持久性为基础--每一种都会产生不同的监管后果。阈值风险评估并不能使监管微塑料的行动合法化,因为微塑料产生毒性影响的阈值需要很高的浓度,以至于工业可以继续排放微塑料几十年。因此,只有与微塑料在持久性和累积性方面的重要性有关的风险评估,才能使监管行动合法化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Agential cuts of regulatory science practices – the case of microplastics
Over the past decades, a new field of research related to microplastics has emerged which still faces a high degree of uncertainty and conflicting views regarding the risks posed by microplastics. To date, social research has not addressed the regulatory science practices necessary for assessing the risks created by microplastics and related ethical questions. Therefore, the objective of this article is to analyse the role of central regulatory science practices, that is, risk assessments as they relate to microplastics. I draw on the work of Karen Barad to conceptualise these regulatory science practices as boundary-drawing practices which produce agential cuts. I will show that scientific and regulatory boundary-drawing practices draw agential cuts determining the properties of microplastics and regulatory actions that have ‘real’ consequences for human and environmental health. My empirical case demonstrates that different versions of risk assessment exist – one based on thresholds and the other on persistence – each of which have different regulatory consequences. Threshold risk assessment does not legitimise action to regulate microplastics, because the threshold at which microplastics have toxic effects requires such high concentrations that industry could continue to emit microplastics for decades. Therefore, only risk assessments that relate to the materiality of microplastics in terms of persistence and accumulation legitimise regulatory action.
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