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多氯联苯在冰川中的分布。2. 沉积和纳入过程的模型结果。

Polychlorinated biphenyls in glaciers. 2. Model results of deposition and incorporation processes.

机构信息

Institute for Chemical and Bioengineering, ETH Zurich , Vladimir-Prelog-Weg 1, CH-8093 Zurich, Switzerland.

出版信息

Environ Sci Technol. 2014 Jul 15;48(14):7849-57. doi: 10.1021/es501793h. Epub 2014 Jul 7.

Abstract

In previous work, Alpine glaciers have been identified as a secondary source of persistent organic pollutants (POPs). However, detailed understanding of the processes organic chemicals undergo in a glacial system was missing. Here, we present results from a chemical fate model describing deposition and incorporation of polychlorinated biphenyls (PCBs) into an Alpine glacier (Fiescherhorn, Switzerland) and an Arctic glacier (Lomonosovfonna, Norway). To understand PCB fate and dynamics, we investigate the interaction of deposition, sorption to ice and particles in the atmosphere and within the glacier, revolatilization, diffusion and degradation, and discuss the effects of these processes on the fate of individual PCB congeners. The model is able to reproduce measured absolute concentrations in the two glaciers for most PCB congeners. While the model generally predicts concentration profiles peaking in the 1970s, in the measurements, this behavior can only be seen for higher-chlorinated PCB congeners on Fiescherhorn glacier. We suspect seasonal melt processes are disturbing the concentration profiles of the lower-chlorinated PCB congeners. While a lower-chlorinated PCB congener is mainly deposited by dry deposition and almost completely revolatilized after deposition, a higher-chlorinated PCB congener is predominantly transferred to the glacier surface by wet deposition and then is incorporated into the glacier ice. The incorporated amounts of PCBs are higher on the Alpine glacier than on the Arctic glacier due to the higher precipitation rate and aerosol particle concentration on the former. Future studies should include the effects of seasonal melt processes, calculate the quantities of PCBs incorporated into the entire glacier surface, and estimate the quantity of chemicals released from glaciers to determine the importance of glaciers as a secondary source of organic chemicals to remote aquatic ecosystems.

摘要

在之前的研究中,阿尔卑斯冰川已被确定为持久性有机污染物(POPs)的次要来源。然而,人们对有机化学物质在冰川系统中经历的过程缺乏详细的了解。在这里,我们展示了一个化学命运模型的结果,该模型描述了多氯联苯(PCBs)在阿尔卑斯冰川(瑞士费斯彻尔霍恩)和北极冰川(挪威的洛蒙诺索夫冰川)中的沉积和结合过程。为了了解 PCB 的命运和动态,我们研究了沉积、在大气中和冰川内部的冰和颗粒上的吸附、再挥发、扩散和降解的相互作用,并讨论了这些过程对单个 PCB 同系物命运的影响。该模型能够再现两个冰川中大多数 PCB 同系物的测量绝对浓度。虽然该模型通常预测浓度剖面在 20 世纪 70 年代达到峰值,但在测量中,这种行为只能在 Fiescherhorn 冰川的高氯化 PCB 同系物中看到。我们怀疑季节性融雪过程扰乱了低氯化 PCB 同系物的浓度剖面。虽然低氯化 PCB 同系物主要通过干沉降沉积,并且在沉积后几乎完全再挥发,但高氯化 PCB 同系物主要通过湿沉降转移到冰川表面,然后被纳入冰川冰中。由于前者的降水率和气溶胶颗粒浓度较高,因此在阿尔卑斯冰川上沉积的 PCB 量高于北极冰川。未来的研究应包括季节性融雪过程的影响,计算纳入整个冰川表面的 PCB 量,并估计从冰川释放的化学物质的数量,以确定冰川作为有机化学物质向偏远水生生态系统的次要来源的重要性。

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