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大西洋海洋表面水域缓冲了大气中持久性有机污染物浓度的下降。

Atlantic ocean surface waters buffer declining atmospheric concentrations of persistent organic pollutants.

机构信息

Centre of Chemicals Management, Lancaster Environment Centre, Lancaster University, Lancaster LA1 4YQ, UK.

出版信息

Environ Sci Technol. 2010 Sep 15;44(18):6978-84. doi: 10.1021/es101293v.

Abstract

Decreasing environmental concentrations of some persistent organic pollutants (POPs) have been observed at local or regional scales in continental areas after the implementation of international measures to curb primary emissions. A decline in primary atmospheric emissions can result in re-emissions of pollutants from the environmental capacitors (or secondary sources) such as soils and oceans. This may be part of the reason why concentrations of some POPs such as polychlorinated biphenyls (PCBs) have not declined significantly in the open oceanic areas, although re-emission of POPs from open ocean water has barely been documented. In contrast, results from this study show that several polychlorinated dibenzo-p-dioxins and furans (PCDD/Fs) have undergone a marked decline (2-3 orders of magnitude for some homologues) over a major portion of the remote oligotrophic Atlantic Ocean. The decline appears to be faster than that observed over continental areas, implicating an important role of oceanic geochemical controls on levels and cycling of some POPs. For several lower chlorinated PCDD/Fs, we observed re-emission from surface water back to the atmosphere. An assessment of the effectiveness of the main sink processes highlights the role of degradation in surface waters as potentially key to explaining the different behavior between PCDD/Fs and PCBs and controlling their overall residence time in the ocean/atmosphere system. This study provides experimental evidence that the ocean has a buffering capacity - dependent on individual chemicals - which moderates the rate at which the system will respond to an underlying change in continental emissions.

摘要

在采取国际措施遏制原始排放后,在大陆地区已经观察到一些持久性有机污染物(POPs)的环境浓度在局部或区域范围内有所降低。原始大气排放的减少会导致污染物从环境电容器(或二次源)如土壤和海洋中重新释放。这可能是某些 POPs 如多氯联苯(PCBs)在开阔海域浓度没有明显下降的部分原因,尽管很少有文献记录开阔海域水中 POPs 的再排放。相比之下,本研究的结果表明,在大部分偏远贫营养大西洋海域,几种多氯二苯并对二恶英和呋喃(PCDD/Fs)的浓度已经明显下降(某些同系物下降了 2-3 个数量级)。下降速度似乎比在大陆地区观察到的更快,这表明海洋地球化学控制对一些 POPs 的水平和循环起着重要作用。对于几种低氯代 PCDD/Fs,我们观察到从地表水重新排放到大气中。对主要汇过程有效性的评估突出了地表水中降解的作用,这可能是解释 PCDD/Fs 和 PCBs 之间不同行为以及控制它们在海洋/大气系统中总停留时间的关键。本研究提供了实验证据,表明海洋具有缓冲能力-取决于个别化学物质-这会调节系统对大陆排放潜在变化的响应速度。

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