Zuo Zi-Cen, Liu Shan-Shan, He Zhen, Yang Gui-Peng
Frontiers Science Center for Deep Ocean Multispheres and Earth System, Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao, 266100, China.
Key Laboratory of Marine Ecology and Environmental Sciences, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Environ Pollut. 2025 Nov 1;384:127021. doi: 10.1016/j.envpol.2025.127021. Epub 2025 Aug 21.
Halogenated polycyclic aromatic hydrocarbons (HPAHs) in marine environment have attracted increasing attention due to their persistence, bioaccumulation potential, and ecological toxicity. However, systematic investigations on their contamination levels, compositional distribution, and source apportionment in the surface sediments of the East China Sea (ECS) remain limited. In this study, 25 HPAHs were quantitatively analyzed in ECS surface sediments, revealing total concentrations ranging from 14.50 to 131.19 ng g dry weight (dw), with a mean value of 42.23 ± 29.60 ng g dw. Notably, brominated PAHs (Br-PAHs: 30.74 ± 24.46 ng g dw) exhibited significantly higher concentrations than chlorinated PAHs (Cl-PAHs: 11.49 ± 6.18 ng g dw). Among the 25 HPAHs, 9-ClFle and 9-BrFle were identified as the most abundant compounds. Total HPAH concentrations across stations correlated positively with water depth, salinity, and dissolved oxygen, but negatively with temperature and chlorophyll a. Spatial patterns showed pronounced heterogeneity, with higher mean values in the south (65.85 ng g dw) than in the north (32.66 ng g dw). This distribution likely reflects combined influences of industrial emissions, hydrodynamic transport, and atmospheric deposition. Positive matrix factorization identified five sources: brominated flame retardant production (27.2 %), petrochemical and electronic waste (21.6 %), metal smelting (6.8 %), transport-related inputs (16.1 %), and regional atmospheric deposition (28.3 %). Ecological risk assessment using bioavailability-adjusted risk quotients (RQ) indicated that brominated congeners posed higher potential risks than chlorinated ones, yet overall risks to aquatic organisms remained below the low-risk threshold. These findings underscore the anthropogenic-environmental interplay shaping HPAH distribution in ECS sediments and inform future management strategies.
海洋环境中的卤代多环芳烃(HPAHs)因其持久性、生物累积潜力和生态毒性而受到越来越多的关注。然而,对其在东海(ECS)表层沉积物中的污染水平、组成分布和源解析的系统研究仍然有限。在本研究中,对东海表层沉积物中的25种HPAHs进行了定量分析,结果显示总浓度范围为14.50至131.19纳克/克干重(dw),平均值为42.23±29.60纳克/克干重。值得注意的是,溴代多环芳烃(Br-PAHs:30.74±24.46纳克/克干重)的浓度显著高于氯代多环芳烃(Cl-PAHs:11.49±6.18纳克/克干重)。在这25种HPAHs中,9-氯芴和9-溴芴被确定为含量最高的化合物。各站位的总HPAH浓度与水深、盐度和溶解氧呈正相关,但与温度和叶绿素a呈负相关。空间格局显示出明显的异质性,南部的平均值(65.85纳克/克干重)高于北部(32.66纳克/克干重)。这种分布可能反映了工业排放、水动力输运和大气沉降的综合影响。正定矩阵因子分解确定了五个来源:溴代阻燃剂生产(27.2%)、石化和电子废物(21.6%)、金属冶炼(6.8%)、交通相关输入(16.1%)和区域大气沉降(28.3%)。使用生物可利用性调整风险商(RQ)进行的生态风险评估表明,溴代同系物比氯代同系物具有更高的潜在风险,但对水生生物的总体风险仍低于低风险阈值。这些发现强调了人为-环境相互作用对东海沉积物中HPAH分布的影响,并为未来的管理策略提供了参考。