Yamashita Nobuyoshi, Taniyasu Sachi, Petrick Gert, Wei Si, Gamo Toshitaka, Lam Paul K S, Kannan Kurunthachalam
National Institute of Advanced Industrial Science and Technology, 16-1 Onogawa, Tsukuba, Ibaraki 305-8569, Japan.
Chemosphere. 2008 Jan;70(7):1247-55. doi: 10.1016/j.chemosphere.2007.07.079. Epub 2007 Sep 12.
Perfluorinated acids (PFAs) such as perfluorooctanesulfonate (PFOS) and perfluorooctanoate (PFOA) are global environmental contaminants. The physicochemical properties of PFAs are unique in that they have high water solubilities despite the low reactivity of carbon-fluorine bond, which also imparts high stability in the environment. Because of the high water solubilities, the open-ocean water column is suggested to be the final sink for PFOS and PFOA. However, little is known on the distribution of PFAs in the oceans around the world. Here we describe the horizontal (spatial) and vertical distribution of PFAs in ocean waters worldwide. PFOS and PFOA concentrations in the North Atlantic Ocean ranged from 8.6 to 36pg l(-1) and from 52 to 338pg l(-1), respectively, whereas the corresponding concentrations in the Mid Atlantic Ocean were 13-73pg l(-1) and 67-439pg l(-1). These were completely different from the surface waters of the South Pacific Ocean and the Indian Ocean (overall range of <5-11pg l(-1) for PFOS and PFOA). Vertical profiles of PFAs in the marine water column were associated with the global ocean circulation theory. Vertical profiles of PFAs in water columns from the Labrador Sea reflected the influx of the North Atlantic Current in surface waters, the Labrador Current in subsurface waters, and the Denmark Strait Overflow Water in deep layers below 2000m. Striking differences in the vertical and spatial distribution of PFAs, depending on the oceans, suggest that these persistent acids can serve as useful chemical tracers to allow us to study oceanic transportation by major water currents. The results provide evidence that PFA concentrations and profiles in the oceans adhere to a pattern consistent with the global "Broecker's Conveyor Belt" theory of open ocean water circulation.
全氟辛酸(PFAs),如全氟辛烷磺酸(PFOS)和全氟辛酸(PFOA),是全球环境污染物。全氟辛酸的物理化学性质独特,尽管碳氟键反应活性低,但它们具有高水溶性,这也使其在环境中具有高稳定性。由于高水溶性,公海水柱被认为是全氟辛烷磺酸和全氟辛酸的最终归宿。然而,关于全氟辛酸在全球海洋中的分布情况知之甚少。在此,我们描述了全球海水中全氟辛酸的水平(空间)和垂直分布。北大西洋中全氟辛烷磺酸和全氟辛酸的浓度分别为8.6至36皮克/升和52至338皮克/升,而中大西洋相应的浓度为13至73皮克/升和67至439皮克/升。这些与南太平洋和印度洋的表层水完全不同(全氟辛烷磺酸和全氟辛酸的总体范围为<5至11皮克/升)。海水中全氟辛酸的垂直分布与全球海洋环流理论相关。拉布拉多海海水柱中全氟辛酸的垂直分布反映了表层水中北大西洋暖流、次表层水中拉布拉多寒流以及2000米以下深层水中丹麦海峡溢流的流入情况。全氟辛酸在垂直和空间分布上的显著差异取决于不同的海洋,这表明这些持久性酸可以作为有用的化学示踪剂,使我们能够研究主要水流的海洋运输。结果提供了证据,表明海洋中全氟辛酸的浓度和分布符合与全球公海“布勒克输送带”环流理论一致的模式。