Division of Analytical and Environmental Toxicology, Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta T6G 2G3, Canada.
Environ Sci Technol. 2011 Sep 1;45(17):7188-94. doi: 10.1021/es2011176. Epub 2011 Aug 8.
Atmospheric deposition of perfluorinated carboxylic acids (PFCAs) in remote regions might arise from transport and degradation of precursors (e.g., perfluorooctanesulfonyl fluoride (PFOSF)-based products or fluorotelomer alcohols (FTOHs)) or direct transport (e.g., PFCAs in the vapor phase or on particles). To probe the dominant atmospheric source of PFCAs, historical trends in environmental FTOH, PFOSF, and direct perfluorooctanoate (PFOA) emissions were compared to the flux of PFCAs (sum of C7-C13 perfluoroalkyl chain lengths) and PFCA isomer signatures in dated sediment cores from two remote alpine lakes in the Canadian Rocky Mountains. Contributions from PFOSF-based substances and direct transport of PFOA were ruled to be minimal because no branched isomers were detected in either core and temporal trends for direct emission of PFOA did not match the flux measurements. PFCA flux to Lake Opabin sediment agreed well with reported FTOH emissions, including a peak in mid-2003 and subsequent decline. In Lake Oesa, agreement between PFCA flux and FTOH emissions was also good up to 2004, but a subsequent decline was only detected for some PFCA congeners through 2008, while others continued to increase. Overall, both the isomer profiles and the temporal trend data suggest that FTOH oxidation is the dominant atmospheric source of PFCAs to these high alpine lakes. The efficacy of recent industry phase-out initiatives was difficult to assess due to the divergent temporal trends in samples after 2003; thus, continued monitoring is suggested at remote sites such as these.
在偏远地区,大气中全氟羧酸(PFCAs)的沉积可能来自于前体(如全氟辛烷磺酰氟(PFOSF)基产品或氟调聚物醇(FTOHs))的传输和降解,或直接传输(如气相中的 PFCAs 或颗粒上的 PFCAs)。为了探究 PFCAs 的主要大气来源,比较了环境 FTOH、PFOSF 和直接全氟辛酸(PFOA)排放的历史趋势与来自加拿大落基山脉两个偏远高山湖泊的年代沉积物核心中 PFCAs(C7-C13 全氟烷基链长度总和)通量和 PFCA 异构体特征。由于在两个核心中均未检测到支链异构体,且直接排放 PFOA 的时间趋势与通量测量结果不匹配,因此排除了 PFOSF 基物质和 PFOA 直接传输的贡献。Opabin 湖沉积物中 PFCA 的通量与报告的 FTOH 排放情况非常吻合,包括 2003 年年中出现峰值,随后出现下降。在 Oesa 湖,直到 2004 年,PFCA 通量与 FTOH 排放之间的吻合度也很好,但随后只有部分 PFCA 同系物的通量在 2008 年之前下降,而其他同系物则继续增加。总的来说,异构体分布和时间趋势数据表明,FTOH 氧化是这些高山湖泊中 PFCAs 的主要大气来源。由于 2003 年后样品的时间趋势存在差异,因此难以评估最近行业淘汰计划的效果;因此,建议在这些偏远地点继续进行监测。