20 Years of Air-Water Gas Exchange Observations for Pesticides in the Western Arctic Ocean

被引:38
|
作者
Jantunen, Liisa M. [1 ]
Wong, Fiona [2 ]
Gawor, Anya [1 ]
Kylin, Henrik [3 ,4 ]
Helm, Paul A. [5 ]
Stern, Gary A. [6 ]
Strachan, William M. J. [7 ]
Burniston, Deborah A. [8 ]
Bidleman, Terry F. [1 ,9 ]
机构
[1] Environm Canada, Air Qual Proc Res Sect, Egbert, ON L0L 1N0, Canada
[2] Stockholm Univ, Analyt Chem & Environm Sci ACES, SE-10691 Stockholm, Sweden
[3] Linkoping Univ, Dept Themat Studies Environm Change, SE-58183 Linkoping, Sweden
[4] North West Univ, Res Unit Environm Sci & Dev, ZA-2520 Potchefstroom, South Africa
[5] Ontario Minist Environm, Environm Monitoring & Reporting Branch, Toronto, ON M9P 3V6, Canada
[6] Univ Manitoba, Ctr Earth Observat Sci, Winnipeg, MB R3T 2N2, Canada
[7] Environm Canada, Aquat Ecosyst Protect Res Div, Burlington, ON L7S 1A1, Canada
[8] Environm Canada, Water Qual Monitoring & Surveillance Sci & Techno, Burlington, ON L7S 1A1, Canada
[9] Umea Univ, Dept Chem, SE-90187 Umea, Sweden
基金
瑞典研究理事会;
关键词
PERSISTENT ORGANIC POLLUTANTS; LONG-RANGE TRANSPORT; ACHIRAL ORGANOCHLORINE PESTICIDES; HENRYS LAW CONSTANTS; NORTH-ATLANTIC; HEXACHLOROCYCLOHEXANES HCHS; ATMOSPHERIC CONCENTRATIONS; POLYCHLORINATED-BIPHENYLS; SPATIAL-DISTRIBUTION; MONITORING STATIONS;
D O I
10.1021/acs.est.5b01303
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The Arctic has been contaminated by legacy organochlorine pesticides (OCPs) and currently used pesticides (CUPs) through atmospheric transport and oceanic currents. Here we report the time trends and air-water exchange of OCPs and CUPs from research expeditions conducted between 1993 and 2013. Compounds determined in both air and water were trans- and cis-chlordanes (TC, CC), trans- and cis-nonachlors (TN, CN), heptachlor exo-epoxide (HEPX), dieldrin (DEL), chlorobomanes (Sigma CHBs and toxaphene), dacthal (DAC), endosulfans and metabolite endosulfan sulfate (ENDO-I, ENDO-II, and ENDO SUL), chlorothalonil (CHT), chlorpyrifos (CPF), and trifluralin (TFN). Pentachloronitrobenzene (PCNB and quintozene) and its soil metabolite pentachlorothianisole (PCTA) were also found in air. Concentrations of most OCPs declined in surface water, whereas some CUPs increased (ENDO-I, CHT, and TFN) or showed no significant change (CPF and DAC), and most compounds declined in air. Chlordane compound fractions TC/(TC + CC) and TC/(TC + CC + TN) decreased in water and air, while CC/(TC + CC + TN) increased. TN/(TC + CC + TN) also increased in air and slightly, but not significantly, in water. These changes suggest selective removal of more labile TC and/or a shift in chlordane sources. Water air fugacity ratios indicated net volatilization (FR > 1.0) or near equilibrium (FR not significantly different from 1.0) for most OCPs but net deposition (FR < 1.0) for Sigma CHBs. Net deposition was shown for ENDO-I on all expeditions, while the net exchange direction of other CUPs varied. Understanding the processes and current state of air surface exchange helps to interpret environmental exposure and evaluate the effectiveness of international protocols and provides insights for the environmental fate of new and emerging chemicals.
引用
收藏
页码:13844 / 13852
页数:9
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