Huang Tao, Luo Duan, Zhou Juan, Li Shuaidong, Xue Jingya, Yang Hao, Li Yunmei, Wang Zaifeng, Huang Changchun
School of Geography, Nanjing Normal University, Nanjing 210023, PR China; Jiangsu Center for Collaborative Innovation in Geographical Information Resource Development and Application, Nanjing Normal University, Nanjing 210023, PR China; Key Laboratory of Virtual Geographic Environment (Nanjing Normal University), Ministry of Education, Nanjing 210023, PR China; State Key Laboratory Cultivation Base of Geographical Environment Evolution (Jiangsu Province), Nanjing 210023, PR China.
School of Geography, Nanjing Normal University, Nanjing 210023, PR China.
Sci Total Environ. 2023 Oct 1;893:164753. doi: 10.1016/j.scitotenv.2023.164753. Epub 2023 Jun 8.
Understanding the source of polycyclic aromatic hydrocarbons (PAHs) is crucial for determining their structural, degradational, and burial characteristics in lake sediments. Here, we used a sediment core to determine the changing sources and burial characteristics of 16 PAHs from Dianchi Lake, southwest China. The ∑PAH concentrations ranged from 105.10 to 1248.05 ng g (448.97 ± 351.25 ng g), exhibiting a sharp increase since 1976. Our results showed that the depositional flux of PAHs has increased by approximately 3.72 times over the past 114 years (1895-2009). The C/N ratio, stable isotopes (δC and δN), and n-alkanes data all indicated that allochthonous contributors of organic carbon have substantially increased since the 1970s, playing an important role in the increase in sedimentary PAHs. Positive matrix factorization indicated that petrogenic sources, coal and biomass combustion, and traffic emissions were the main sources of PAHs. The relationships between PAHs from different sources and total organic carbon (TOC) varied with the sorption characteristics. The effect of TOC on the absorption of high-molecular-weight aromatic PAHs from fossil fuels was significant. A higher risk of lake eutrophication is accompanied by higher allochthonous organic matter imports, which might stimulate an increase in sedimentary PAHs through algal biomass blooms.
了解多环芳烃(PAHs)的来源对于确定其在湖泊沉积物中的结构、降解和埋藏特征至关重要。在此,我们利用一个沉积物岩芯来确定中国西南部滇池16种多环芳烃的来源变化和埋藏特征。∑PAH浓度范围为105.10至1248.05 ng g(448.97±351.25 ng g),自1976年以来呈急剧上升趋势。我们的结果表明,在过去114年(1895 - 2009年)中,多环芳烃的沉积通量增加了约3.72倍。C/N比、稳定同位素(δC和δN)以及正构烷烃数据均表明,自20世纪70年代以来,有机碳的异地贡献者大幅增加,在沉积多环芳烃的增加中发挥了重要作用。正定矩阵因子分解表明,成岩源、煤炭和生物质燃烧以及交通排放是多环芳烃的主要来源。不同来源的多环芳烃与总有机碳(TOC)之间的关系随吸附特征而变化。TOC对来自化石燃料的高分子量芳香多环芳烃的吸附作用显著。湖泊富营养化风险越高,伴随着异地有机质输入越高,这可能通过藻类生物量爆发刺激沉积多环芳烃的增加。