School of Marine Sciences, Sun Yat-sun University, Zhuhai, 519082, China; Ministry of Education Key Laboratory for Coastal and Island Development, Nanjing University, Nanjing, 210093, China; Southern Marine Science and Engineering Guangdong Laboratory, Zhuhai, 519080, China; Department of Physical and Environmental Science, Texas A&M University Corpus Christi, 78412, USA.
Graduate School of Oceanography, University of Rhode Island, Narragansett, RI, 02882, USA.
Environ Pollut. 2020 Oct;265(Pt A):114956. doi: 10.1016/j.envpol.2020.114956. Epub 2020 Jun 10.
Surface seawater and lower atmosphere gas samples were collected simultaneously between 18°N and 40°S in the open Pacific Ocean in 2006-2007. Samples were analyzed for organochlorine pesticides (OCPs) to assess their distribution patterns, the role of ocean in the long-range transport (LRT), and the air-water exchange directions in the open Pacific Ocean. Such open ocean studies can yield useful information such as establishing temporal and spatial trends and assessing primary vs secondary emissions of legacy OCPs. Target compounds included hexachlorocyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs) and its derivatives, and chlordane compounds. Concentrations for α-HCH, γ-HCH, trans-chlordane (TC), and cis-chlordane (CC) were higher in the Northern Hemisphere (NH) than the Southern Hemisphere (SH) in both gaseous and dissolved phases, while the distribution patterns of DDTs and heptachlor exo-epoxide (HEPX) showed a reversed pattern. In the N Pacific, concentrations of α-HCH and γ-HCH in the present work were lower by 63 and 16 times than those observed in 1989-1990. The distribution patterns of DDT suggested there was usage in the SH around 2006. Calculated fugacity ratios suggested that γ-HCH was volatilizing from surface water to the atmosphere, and the air-water exchange fluxes were 0.3-11.1 ng m day. This is the first field study that reported the open Pacific Ocean has become the secondary source for γ-HCH and implied that ocean could affect LRT of OCPs by supplying these compounds via air-sea exchange.
2006-2007 年,在太平洋开阔海域北纬 18°至南纬 40°之间同步采集了表层海水和底层大气气体样本。对有机氯农药(OCPs)进行了分析,以评估其分布模式、海洋在长距离传输(LRT)中的作用,以及开阔太平洋的气-水交换方向。这种开阔海域的研究可以提供有用的信息,例如确定时空趋势和评估 OCPs 的原始排放与次生排放。目标化合物包括六氯环己烷(HCHs)、滴滴涕(DDTs)及其衍生物和氯丹化合物。α-HCH、γ-HCH、反式氯丹(TC)和顺式氯丹(CC)在气、液相中的浓度在北半球(NH)均高于南半球(SH),而 DDTs 和七氯 exo-环氧化物(HEPX)的分布模式则呈现相反的模式。在北太平洋,本研究中 α-HCH 和 γ-HCH 的浓度分别比 1989-1990 年观察到的浓度低 63 倍和 16 倍。DDTs 的分布模式表明,2006 年左右在 SH 地区仍在使用 DDT。计算的逸度比表明,γ-HCH 正在从表层水挥发到大气中,气-水交换通量为 0.3-11.1ng m-2 d-1。这是第一项报道开阔太平洋已成为 γ-HCH 的次生源的实地研究,并暗示海洋可以通过气-海交换向大气中提供这些化合物,从而影响 OCPs 的 LRT。