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北大西洋和北冰洋地表水及大气中的有机氯农药和多环芳烃。

Organochlorine pesticides and PAHs in the surface water and atmosphere of the North Atlantic and Arctic Ocean.

作者信息

Lohmann Rainer, Gioia Rosalinda, Jones Kevin C, Nizzetto Luca, Temme Christian, Xie Zhiyong, Schulz-Bull Detlef, Hand Ines, Morgan Eric, Jantunen Liisa

机构信息

Graduate School of Oceanography, University of Rhode Island, Narragansett, Rhode Island 02882, USA.

出版信息

Environ Sci Technol. 2009 Aug 1;43(15):5633-9. doi: 10.1021/es901229k.

Abstract

Surface seawater and boundary layer atmospheric samples were collected on the FS Polarstern during cruise ARKXX in the North Atlantic and Arctic Ocean in 2004. Samples were analyzed for persistent organic pollutants (POPs), with a focus on organochlorine pesticides, including hexachlorocyclohexanes (HCHs), chlordanes, DDTs, hexachlorobenzene (HCB), and polycyclic aromatic hydrocarbons. In addition, the enantiomer fractions (EFs) of pesticides, notably alpha-HCH and cis-chlordane (CC), were determined. Concentrations of dissolved HCB increased from near Europe (approximately 1-2 pg/L) toward the high Arctic (4-10 pg/L). For dissolved HCB, strongest correlations were obtained with the average air or water temperature during sampling, not latitude. In the western Arctic Ocean, surface waters with elevated concentrations of HCB (5-10 pg/ L) were flowing out of the Arctic Ocean as part of the East Greenland current In contrast to dissolved compounds, atmospheric POPs did not display trends with temperature. Air-water exchange gradients suggested net deposition for all compounds, though HCB was closest to air-water equilibrium. EFs for alpha-HCH in seawater ranged from 0.43 to 0.50, except for two samples from 75 degrees N in the East Greenland Sea, with EFs of 0.31 and 0.37. Lowest EF (0.47) for CC were also at 75 degrees N, other samples had EFs from 0.49 to 0.52. It is suggested that samples from around 75 degrees N in the Greenland Gyre represented a combination of surface and older/deeper Arctic water.

摘要

2004年,在“极地号”科考船执行北大西洋和北冰洋的ARKXX航次期间,采集了表层海水和边界层大气样本。对样本进行了持久性有机污染物(POPs)分析,重点是有机氯农药,包括六氯环己烷(HCHs)、氯丹、滴滴涕(DDTs)、六氯苯(HCB)和多环芳烃。此外,还测定了农药的对映体分数(EFs),特别是α-HCH和顺式氯丹(CC)。溶解态HCB的浓度从欧洲附近(约1-2 pg/L)向北极高纬度地区(4-10 pg/L)增加。对于溶解态HCB,与采样期间的平均气温或水温相关性最强,而非与纬度。在北冰洋西部,HCB浓度升高(5-10 pg/L)的表层水作为东格陵兰洋流的一部分流出北冰洋。与溶解态化合物不同,大气中的POPs没有呈现出随温度变化的趋势。气-水交换梯度表明所有化合物均有净沉降,不过HCB最接近气-水平衡。海水中α-HCH的EFs范围为0.43至0.50,但在东格陵兰海北纬75度的两个样本中,EFs分别为0.31和0.37。CC的最低EF(0.47)也出现在北纬75度,其他样本的EFs为0.49至0.52。有人认为,格陵兰环流中北纬75度附近的样本代表了表层水与较老/较深的北极水的混合。

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