Key Laboratory of Mariculture (Ocean University of China), Ministry of Education, Qingdao, People's Republic of China.
Shandong Marine Resources and Environment Research Institute, Shandong Provincial Key Laboratory of Restoration for Marine Ecology, Yantai, 264006, People's Republic of China.
Environ Res. 2024 Apr 15;247:118214. doi: 10.1016/j.envres.2024.118214. Epub 2024 Jan 19.
The contaminant status, spatial distribution, partitioning behavior, and ecological risks of 26 legacy and emerging perfluoroalkyl and polyfluoroalkyl substances (PFASs) in Laizhou Bay, China were investigated. The concentrations of ∑PFASs in surface and bottom seawater ranged from 37.2 to 222 ng/L and from 34.2 to 305 ng/L with an average of 116 ± 62.7 and 138 ± 93.8 ng/L, respectively. There were no significant differences in the average concentrations between the surface and bottom seawater (P > 0.05). Perfluorooctanoic acid (PFOA) and short-chain PFASs dominated the composition of PFASs in seawater. The concentrations of ∑PFASs in sediments ranged from 0.997 to 7.21 ng/g dry weight (dw), dominated by perfluorobutane sulfonate (PFBS), perfluorobutanoic acid (PFBA), and long-chain PFASs. The emerging alternatives of perfluoro-1-butane-sulfonamide (FBSA) and 6:2 fluorotelomer sulfonic acid (6:2 FTSA) were detected for the first time in Laizhou Bay. The ∑PFASs in seawater in the southwest of the bay were higher than those in the northeast of the bay. The ∑PFASs in sediments in the northeast sea area were higher than those in the inner area of the bay. Log K and log K values increased with increasing carbon chain length for PFASs compounds. Ecological risk assessments indicated a low ecological risk associated with HFPO-DA but a moderate risk associated with PFOA contamination in Laizhou Bay. Positive matrix factorization (PMF) analysis revealed that fluoropolymer manufacturing, metal plating plants, and textile treatments were identified as major sources contributing to PFASs contamination.
本研究调查了中国莱州湾 26 种 legacy 和新兴全氟烷基和多氟烷基物质 (PFASs) 的污染状况、空间分布、分配行为和生态风险。表层和底层海水中∑PFASs 的浓度范围分别为 37.2-222ng/L 和 34.2-305ng/L,平均值分别为 116±62.7ng/L 和 138±93.8ng/L。表层和底层海水中∑PFASs 的平均浓度无显著差异(P>0.05)。全氟辛酸(PFOA)和短链 PFASs 是海水 PFASs 组成的主要成分。沉积物中∑PFASs 的浓度范围为 0.997-7.21ng/g 干重(dw),主要由全氟丁烷磺酸盐(PFBS)、全氟丁酸(PFBA)和长链 PFASs 组成。首次在莱州湾检测到全氟-1-丁烷磺酰胺(FBSA)和 6:2 氟代烷烃磺酸盐(6:2 FTSA)这两种新兴替代品。湾西南部海水中∑PFASs 的浓度高于湾东北部。湾东北部海域沉积物中∑PFASs 的浓度高于湾内海域。海水中 PFASs 化合物的 log K 和 log K 值随碳链长度的增加而增加。生态风险评估表明,HFPO-DA 相关的生态风险较低,而 PFOA 污染相关的生态风险为中度。正定矩阵因子分析(PMF)结果表明,氟聚合物制造、电镀厂和纺织品处理是导致 PFASs 污染的主要来源。