Zhang Qian, Song Jin-Ming, Peng Quan-Cai, Li Xue-Gang, Yuan Hua-Mao, Li Ning, Duan Li-Qin, Qu Bao-Xiao, Wang Qi-Dong
CAS Key Laboratory of Marine Ecology and Environmental Sciences, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China.
College of Earth Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Huan Jing Ke Xue. 2017 Jul 8;38(7):2763-2772. doi: 10.13227/j.hjkx.201701016.
Hydrocarbons emitted by human activities probably constitute the largest class of contaminants that are present in coastal areas, because of widespread use of fossil fuels for power generation and logistics, and accidental spillages. The chemical composition of hydrocarbon mixtures found in the marine environment allowed the identification of relative contributions of different natural and anthropogenic sources. Identification of these hydrocarbons, especially -alkanes, could act as tracers for the possible sources. To evaluate -alkanes concentrations with emphasis on source analysis, surface water without visible oil was collected from the cruise in April 2016. Determination and quantification were performed by solvent extraction and gas chromatography-mass spectrometry. Various molecular diagnostic parameters were used to assess the contribution of different sources and origin of -alkanes in surface seawater of Jiaozhou Bay. Concentrations of total dissolved -alkanes(C-C) were between 1.756-39.09 μg·L with a high carbon number predominance profile without odd-even carbon number preference. The -alkane concentrations varied spatially depending on the distance away from main input sources and the ability of water exchange. It was at a higher concentration in the northeast and west coastal areas, as well as the mouth of Jiaozhou Bay. And concentrations were relatively lower in the inner area and outside of Jiaozhou Bay. In the sea area with strong water exchange, concentrations of total -alkanes were around 2.196 μg·L, which could be considered as the environmental background level of -alkanes in Jiaozhou Bay. Those -alkanes were dominated with C, with a slightly odd carbon number preference in low carbon -alkanes and an even carbon number preference in high carbon -alkanes. The values of CPI for the whole range of -alkanes series, low carbon -alkanes, and high carbon -alkanes were 0.949, 1.026, and 0.980, respectively. Diagnostic indices and curves indicated that the dominant inputs of those -alkanes were from marine biogenic input such as algae and marine bacteria. The concentration profiles of -alkanes in other areas were characterized by no odd-even predominance in the range of C-C with peaks center at C which were indicative of anthropic contributions as emission sources. -alkanes dominating with anthropic sources comprised a high proportion(83.7%) of total -alkanes. Activities of harbors and ships were the main contributors of Jiaozhou Bay -alkanes. Physical processes, such as evaporation and dilution, were the principal weathering mechanisms. Because of its sufficient environmental capacity, Jiaozhou Bay was still moderately contaminated with petroleum.
由于化石燃料在发电和物流中的广泛使用以及意外泄漏,人类活动排放的碳氢化合物可能是沿海地区存在的最大一类污染物。根据在海洋环境中发现的碳氢化合物混合物的化学成分,可以确定不同自然和人为来源的相对贡献。识别这些碳氢化合物,尤其是正构烷烃,可以作为可能来源的示踪剂。为了评估正构烷烃浓度并重点进行源分析,于2016年4月从航次中采集了无可见油污的地表水。通过溶剂萃取和气相色谱 - 质谱联用进行测定和定量。使用各种分子诊断参数来评估胶州湾表层海水中不同来源和正构烷烃来源的贡献。总溶解正构烷烃(C₁₀ - C₃₅)的浓度在1.756 - 39.09 μg·L之间,具有高碳数优势分布,没有奇偶碳数偏好。正构烷烃浓度在空间上因距主要输入源的距离和水交换能力而异。在东北和西部沿海地区以及胶州湾口浓度较高。而在胶州湾内部和外部区域浓度相对较低。在水交换强烈的海域,总正构烷烃浓度约为2.196 μg·L,可视为胶州湾正构烷烃的环境背景水平。这些正构烷烃以C₂₇为主,低碳正构烷烃略有奇数碳数偏好,高碳正构烷烃有偶数碳数偏好。整个正构烷烃系列、低碳正构烷烃和高碳正构烷烃的CPI值分别为0.949、1.026和0.980。诊断指数和曲线表明,这些正构烷烃的主要输入来自藻类和海洋细菌等海洋生物源输入。其他区域正构烷烃的浓度分布特征是在C₁₀ - C₃₅范围内无奇偶优势,峰值中心在C₂₃,这表明存在人为排放源的贡献。以人为源为主的正构烷烃占总正构烷烃的比例较高(83.7%)。港口和船舶活动是胶州湾正构烷烃的主要贡献者。蒸发和稀释等物理过程是主要的风化机制。由于其足够的环境容量,胶州湾仍受到石油的中度污染。