Marine Bioresource and Environment Research Center, Key Laboratory of Marine Eco-Environmental Science and Technology, First Institute of Oceanography, Ministry of Natural Resources, Qingdao 266061, China; Laboratory for Marine Ecology and Environmental Science, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao 266071, China; Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao 266100, China; Qingdao Key Laboratory of Analytical Technology Development and Standardization of Chinese Medicines, Qingdao 266590, China.
Marine Bioresource and Environment Research Center, Key Laboratory of Marine Eco-Environmental Science and Technology, First Institute of Oceanography, Ministry of Natural Resources, Qingdao 266061, China; Laboratory for Marine Ecology and Environmental Science, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao 266071, China; Qingdao Key Laboratory of Analytical Technology Development and Standardization of Chinese Medicines, Qingdao 266590, China.
J Hazard Mater. 2022 Sep 5;437:129264. doi: 10.1016/j.jhazmat.2022.129264. Epub 2022 Jun 1.
The contamination status and transport of per- and polyfluoroalkyl substances (PFASs) in the seawater of the Indian Ocean (IO) and an adjacent subregion of the Northwest Pacific Ocean (NWPO) were investigated. Eight legacy PFASs were widely distributed in the surface seawater, and perfluoroheptanoic acid (PFHpA) and perfluorooctanoic acid (PFOA) were the two predominant PFASs. ΣPFAS concentration decreased in the following order: NWPO>Joining area of Asia and Indian-Pacific Oceans (JAIPO)>Northeast Indian Ocean>Southwest Indian Ocean. Hexafluoropropylene oxide-dimer acid, a replacement surfactant for PFOA was extensively detected in the IO (~34.8 pg/L) for the first time, showing an early sign of emerging PFAS spread in global open oceans. Eight depth profiles across the JAIPO (down to 5433 m depth) revealed a "surface-enrichment" and "depth-depletion" pattern for PFASs in the water column, and two noticeable fluctuations were mainly located at depths of 150-200 and 200-500 m. Physical processes, including eddy diffusion, and the origin and trajectory of water mass were crucial factors for structuring PFAS vertical profiles. Mass transport estimates revealed a remarkable PFOA contribution through the JAIPO to IO carried by the Indonesian Throughflow, and a nonnegligible PFHpA contribution from Antarctic Immediate Water to deep water of the JAIPO driven by thermohaline circulation.
调查了印度洋(IO)和西北太平洋(NWPO)邻近海域海水中全氟和多氟烷基物质(PFASs)的污染状况和迁移情况。八种传统 PFASs 在表层海水中广泛分布,其中全氟庚酸(PFHpA)和全氟辛酸(PFOA)是两种主要的 PFASs。ΣPFAS 浓度的顺序为:NWPO>亚洲和印度洋-太平洋连接区(JAIPO)>东北印度洋>西南印度洋。六氟丙烯氧化物二聚酸,一种 PFOA 的替代表面活性剂,首次在印度洋中被广泛检出(约 34.8 pg/L),表明新兴 PFAS 在全球开阔海域传播的早期迹象。JAIPO 八个深度剖面(深达 5433 米)揭示了水柱中 PFASs 的“表面富集”和“深度耗尽”模式,两个明显的波动主要位于 150-200 和 200-500 米深度。包括涡扩散在内的物理过程,以及水团的来源和轨迹,是构成 PFAS 垂直分布的关键因素。物质输运估算表明,印度尼西亚海流通过 JAIPO 将大量 PFOA 输送到 IO,而由温盐环流驱动的南极瞬时水通过 JAIPO 向深层水输送的 PFHpA 也不容忽视。