Garnett Jack, Halsall Crispin, Vader Anna, Joerss Hanna, Ebinghaus Ralf, Leeson Amber, Wynn Peter M
Lancaster Environment Centre, Lancaster University, Lancaster LA1 4YQ, U.K.
Department of Arctic Biology, The University Centre in Svalbard (UNIS), Longyearbyen N-9170, Norway.
Environ Sci Technol. 2021 Aug 17;55(16):11049-11059. doi: 10.1021/acs.est.1c01676. Epub 2021 Jul 26.
Poly- and perfluoroalkyl substances are synthetic chemicals that are widely present in the global environment including the Arctic. However, little is known about how these chemicals (particularly perfluoroalkyl acids, PFAA) enter the Arctic marine system and cycle between seawater and sea ice compartments. To evaluate this, we analyzed sea ice, snow, melt ponds, and near-surface seawater at two ice-covered stations located north of the Barents Sea (81 °N) with the aim of investigating PFAA dynamics in the late-season ice pack. Sea ice showed high concentrations of PFAA particularly at the surface with snow-ice (the uppermost sea ice layer strongly influenced by snow) comprising 26-62% of the total PFAA burden. Low salinities (<2.5 ppt) and low δO values (<1‰ in snow and upper ice layers) in sea ice revealed the strong influence of meteoric water on sea ice, thus indicating a significant atmospheric source of PFAA with subsequent transfer down the sea ice column in meltwater. Importantly, the under-ice seawater (0.5 m depth) displayed some of the highest concentrations notably for the long-chain PFAA (e.g., PFOA 928 ± 617 pg L), which were ≈3-fold higher than those of deeper water (5 m depth) and ≈2-fold higher than those recently measured in surface waters of the North Sea infuenced by industrial inputs of PFAAs. The evidence provided here suggests that meltwater arising early in the melt season from snow and other surface ice floe components drives the higher PFAA concentrations observed in under-ice seawater, which could in turn influence the timing and extent of PFAA exposure for organisms at the base of the marine food web.
多氟烷基和全氟烷基物质是一类合成化学品,广泛存在于包括北极在内的全球环境中。然而,对于这些化学品(特别是全氟烷基酸,PFAA)如何进入北极海洋系统以及在海水和海冰隔室之间循环,我们知之甚少。为了评估这一点,我们分析了位于巴伦支海以北(北纬81°)的两个冰封站点的海冰、雪、融水池和近表层海水,目的是研究晚季冰盖中PFAA的动态变化。海冰中PFAA浓度很高,特别是在雪冰(受雪强烈影响的最上层海冰)占总PFAA负荷26 - 62%的表面。海冰中的低盐度(<2.5 ppt)和低δO值(雪和上层冰层中<1‰)揭示了大气降水对海冰的强烈影响,这表明PFAA有显著的大气来源,随后通过融水向下输送到海冰柱中。重要的是,冰下海水中(深度0.5米)某些长链PFAA的浓度显著最高(例如,全氟辛酸928 ± 617 pg/L),比深层水(深度5米)高约3倍,比最近在受PFAA工业输入影响的北海表层水中测得的浓度高约2倍。此处提供的证据表明,融冰季节早期雪和其他表层浮冰成分产生的融水导致了冰下海水中较高的PFAA浓度,这反过来可能会影响海洋食物网底层生物接触PFAA的时间和程度。