Per- and poly-fluoroalkyl substances (PFAS) contamination of surface waters by historic landfills via groundwater plumes: ecosystem exposure and downstream mass loading†
J. W. Roy, V. R. Propp, T. Hua, S. J. Brown, C. Brinovcar, J. E. Smith and A. O. De Silva
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引用次数: 0
Abstract
Many historic landfill sites have groundwater plumes that discharge to nearby surface waters. Recent research indicates that leachate of historic landfills can contain elevated concentrations of per- and polyfluoroalkylated substances (PFAS), but there is limited data on resulting PFAS inputs to aquatic ecosystems as might inform on this potential environmental threat. The objective of this study was to evaluate PFAS exposure in three ecological zones and PFAS mass loading downstream, over 1 year, at two historic landfill sites where landfill plumes discharge to nearby surface waters (1 pond with outlet stream, called HB site; 1 urban stream, called DC site). The three zones experienced different magnitudes and patterns of PFAS concentration exposure (i.e., contaminant presence in the zone). The endobenthic zone of the sediments receiving the landfill plumes experienced the highest concentrations (∑PFAS >4000 ng L−1 (HB) and >20 000 ng L−1 (DC)), often year-round and over a substantial area at each site. Dilution of landfill PFAS in surface waters was observed though concentrations were still elevated (∑PFAS: >120 ng L−1 (HB) and >60 ng L−1 (DC)), with evidence of year-round pelagic zone exposure. PFAS concentrations in the epibenthic zones could vary between that of the endobenthic and pelagic zones, sometimes with daily, event-based, and longer-term patterns. Together these findings suggest historic landfill plumes can lead to substantial PFAS exposure to a variety of aquatic life. Downstream PFAS mass loadings during base flows were relatively small individually (15 (HB) and 36 (DC) g per year (∑PFAS)); however, collective loadings from the numerous historic landfills in a watershed could contribute to increasing PFAS concentrations of connected water bodies, with implications for ecological health, drinking water sources, and fisheries.
许多历史上的垃圾填埋场都有地下水排放到附近的地表水中。最近的研究表明,历史上的垃圾填埋场的渗滤液可能含有高浓度的全氟烷基和多氟烷基物质(PFAS),但关于由此产生的全氟烷基物质对水生生态系统的投入的数据有限,无法为这种潜在的环境威胁提供信息。本研究的目的是评估三个生态区的PFAS暴露和下游PFAS的质量负荷,超过1年,在两个历史悠久的垃圾填埋场,垃圾填埋柱排放到附近的地表水(1个有出口流的池塘,称为HB站点;1 .城市流,称为DC站点)。三个区域的PFAS浓度暴露(即污染物在该区域的存在)的程度和模式不同。接收垃圾填埋场羽流沉积物的底栖生物区经历了最高的浓度(∑PFAS >4000 ng L-1 (HB)和>20 000 ng L-1 (DC)),通常是全年的,并且在每个站点都有相当大的面积。尽管浓度仍然升高(∑PFAS: >120 ng L-1 (HB)和>60 ng L-1 (DC)),但地表水中填埋PFAS被稀释,有证据表明其常年暴露于上层水域。底栖生物带的PFAS浓度可能在底栖生物带和中上层生物带之间变化,有时具有每日、基于事件和长期的模式。综上所述,这些发现表明,历史上的垃圾填埋场烟雾会导致大量的PFAS暴露于各种水生生物中。基流期间下游PFAS质量负荷相对较小(15 (HB)和36 (DC) g /年(∑PFAS));然而,来自流域内众多历史垃圾填埋场的集体负荷可能导致相关水体中PFAS浓度的增加,从而对生态健康、饮用水源和渔业产生影响。
期刊介绍:
Environmental Science: Processes & Impacts publishes high quality papers in all areas of the environmental chemical sciences, including chemistry of the air, water, soil and sediment. We welcome studies on the environmental fate and effects of anthropogenic and naturally occurring contaminants, both chemical and microbiological, as well as related natural element cycling processes.