Frontiers Science Center for Deep Ocean Multispheres and Earth System, and Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao 266100, China.
Frontiers Science Center for Deep Ocean Multispheres and Earth System, and Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao 266100, China; Laboratory for Marine Ecology and Environmental Science, Qingdao Marine Science and Technology Center, Qingdao 266237, China; Institute of Marine Chemistry, Ocean University of China, Qingdao 266100, China.
Water Res. 2024 Nov 15;266:122372. doi: 10.1016/j.watres.2024.122372. Epub 2024 Sep 2.
Benzothiazoles (BTHs), benzotriazoles (BTRs), and benzotriazole ultraviolet absorbers (BUVs) have garnered significant attention owing to their persistent nature in the environment and adverse impacts on aquatic organisms. However, there remains a dearth of investigations and studies conducted in tropical marine environments. In this study, we undertook the inaugural distributional survey and ecotoxicological relevance of BTHs, BTRs, and BUVs in seawater and sediments of the western South China Sea (WSCS). Elevated concentrations of BTHs, BTRs, and BUVs in the seawater and suspended particulate matter (SPM) were primarily observed in the Pearl River Estuary (PRE) and the western region of the WSCS, attributed to terrestrial runoff and hydrodynamic processes. Moreover, the transport of these compounds at the seawater-SPM interface was influenced by both the intrinsic properties of the contaminants and temperature variations. Spatially, concentrations of BTHs, BTRs, and BUVs in surface sediments exhibited a diminishing trend with increasing distance from the coast to offshore areas, reflecting notable anthropogenic impacts. Concentration profiles of these compounds in sediment cores displayed a bottom-up increasing trend, with total organic carbon (TOC) identified as the primary determinant governing their accumulation within sediment cores in the WSCS. Terrestrial runoff inputs and atmospheric deposition as major contributors to the occurrence of BTHs, BTRs, and BUVs in the WSCS. Simultaneously, the study underscores the non-negligible moderate mixture risk quotient associated with BTHs, BTRs, and BUVs in the sediments.
苯并噻唑类(BTHs)、苯并三唑类(BTRs)和苯并三唑紫外线吸收剂(BUVs)由于其在环境中的持久性和对水生生物的不利影响而受到广泛关注。然而,在热带海洋环境中,对它们的研究仍然很少。在这项研究中,我们首次对南海西部(WSCS)海水中和沉积物中 BTHs、BTRs 和 BUVs 的分布情况和生态毒理学相关性进行了调查。珠江口(PRE)和 WSCS 西部海域的海水中和悬浮颗粒物(SPM)中 BTHs、BTRs 和 BUVs 的浓度较高,这主要是由于陆地径流和水动力过程造成的。此外,这些化合物在海水-SPM 界面的传输受到污染物固有特性和温度变化的影响。从空间上看,表层沉积物中 BTHs、BTRs 和 BUVs 的浓度随着离海岸距离的增加而呈递减趋势,反映出显著的人为影响。沉积物芯中这些化合物的浓度分布呈现出由底部向上增加的趋势,总有机碳(TOC)被确定为控制 WSCS 中它们在沉积物芯中积累的主要因素。陆地径流输入和大气沉降是 WSCS 中 BTHs、BTRs 和 BUVs 存在的主要原因。同时,该研究强调了 BTHs、BTRs 和 BUVs 在沉积物中存在不可忽视的中等混合风险商数。