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北海生产水中多环芳烃对大西洋鳕鱼早期生活阶段的暴露和吸收。

North sea produced water PAH exposure and uptake in early life stages of Atlantic Cod.

机构信息

SINTEF Ocean, Trondheim, Norway.

SINTEF Ocean, Trondheim, Norway.

出版信息

Mar Environ Res. 2021 Jan;163:105203. doi: 10.1016/j.marenvres.2020.105203. Epub 2020 Oct 27.

DOI:10.1016/j.marenvres.2020.105203
PMID:33160645
Abstract

Produced water discharges from offshore oil and gas platforms represent a significant source of petroleum components such as polycyclic aromatic hydrocarbons (PAHs) released to the ocean. High molecular weight PAHs are persistent in the environment and have a potential for bioaccumulation, and the investigation of their fate and uptake pathways in marine life are relevant when assessing environmental risk of produced water discharges. To study the exposure and uptake of 2-5 ring PAHs in early life stages of Atlantic Cod in the North Sea, we run a coupled fate and individual-based numerical model that includes discharges from 26 platforms. We consider 26 different PAH components in produced water which biodegrade with primary degradation rates; intermediate degradation products are not included. Model simulations are run covering multiple years (2009-2012) to study annual exposure variability, while a one-day time slice of spawning products from the peak spawning season are followed. By covering multiple release points and large spatio-temporal scales, we show how individuals can be exposed to produced water from multiple regions in the North Sea. We find that a combination of oceanic fate processes and toxicokinetics lead to markedly different compositions in the predicted internal concentrations of PAHs compared to discharge concentrations; for instance, naphthalene makes up 30% of the total discharged PAHs, but contributes to at most 1% of internal concentrations. In all simulations we find the predicted total internal PAH concentration (26 components) to be below 1.2 nmol/g, a factor of 1000 less than concentrations commonly associated with acute narcotic effects.

摘要

近海石油和天然气平台产生的生产水排放物是释放到海洋中的石油成分(如多环芳烃 (PAHs))的重要来源。高分子量 PAHs 在环境中具有持久性,并且具有生物累积的潜力,因此在评估生产水排放物的环境风险时,研究其在海洋生物中的归宿和摄取途径非常重要。为了研究北大西洋鳕鱼早期生活阶段中 2-5 环 PAHs 的暴露和摄取情况,我们运行了一个耦合的归宿和基于个体的数值模型,其中包括 26 个平台的排放物。我们考虑了生产水中的 26 种不同的 PAH 成分,这些成分具有初始降解速率;中间降解产物不包括在内。模型模拟运行覆盖了多年(2009-2012 年),以研究年度暴露变异性,同时还跟踪了产卵高峰期的产卵产品的一天时间切片。通过覆盖多个释放点和大的时空尺度,我们展示了个体如何能够接触到北海多个区域的生产水。我们发现,海洋归宿过程和毒代动力学的组合导致预测的内部 PAH 浓度与排放浓度相比具有明显不同的组成;例如,萘占总排放 PAHs 的 30%,但对内部浓度的贡献最多为 1%。在所有模拟中,我们发现预测的总内部 PAH 浓度(26 种成分)低于 1.2 nmol/g,这是与急性麻醉作用相关的浓度的 1000 倍。

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