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Distribution and source recognition of polycyclic aromatic hydrocarbons in the sediments of Hsin-ta Harbour and adjacent coastal areas, Taiwan

机译:台湾新大港及邻近沿海地区沉积物中多环芳烃的分布及来源识别

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摘要

Thirty-three sediment samples from Hsin-ta Harbour and neighboring coastal areas were analyzed by GC-MS for polycyclic aromatic hydrocarbons (PAHs). Total concentrations of 30 analyzed parental and alkylated PAHs (∑PAH) varied from 98.1 to 3382 ng/g dry weight. MP/P (methylphenanthrenes/phenanthrene) values larger than 2 coincided with very low P/A (phenanthrene/ anthracene) values at inner harbour stations, revealing that a significant portion of low molecular weight PAHs are probably from petrogenic pollution sources, specifically, illegal disposal of used motor oil. The 4,6-dimethyldibenzothiophene/3,6-dimethylphen-anthrene (4,6-C_2D/3,6-C_2P) ratio is found to be more useful than the MP/P ratio in tracing petrogenic PAHs from the inner harbour area to the adjacent coastal environment. In addition, according to hierarchical cluster analysis, collected sediments cluster in three major groups, Off-shore Group, Near-shore Group and Inner Harbour Group. Three diagnostic ratios, 4,6-C_2D/3,6-C_2P, PER/∑PAH (perylene to ∑PAH) and BaA/CHR (benzo(a)anthracene/chrysene), representing petrogenic, biogenic and pyrogenic origins, are found to be effective in differentiating and characterizing sediments among the groups in this study. Enrichment of pyrogenic and petrogenic PAHs in sediments collected exhibits mixing or dilution, spatially, by biogenic (or natural) PAHs.
机译:通过GC-MS分析了来自新大港和邻近沿海地区的33个沉积物样品中的多环芳烃(PAHs)。 30种分析的亲代和烷基化PAH(∑PAH)的总浓度在98.1至3382 ng / g干重之间。 MP / P(甲基菲/菲)值大于2的同时,内港站的P / A(菲/蒽)值也很低,这表明低分子量PAH的很大一部分可能来自于成因污染源,特别是非法处置用过的机油。发现4,6-二甲基二苯并噻吩/ 3,6-二甲基苯并菲(4,6-C_2D / 3,6-C_2P)比MP / P比在追踪从内港区到成因的PAH时更有用邻近的沿海环境。此外,根据层次聚类分析,收集的沉积物聚类分为三个主要组,近海组,近海组和内港组。发现了三个诊断比率,分别代表成因,生物成因和热成因,分别为4,6-C_2D / 3,6-C_2P,PER / ∑PAH(to与∑PAH)和BaA / CHR(苯并(a)蒽/丙烯)。在本研究中可有效区分各组中的沉积物。收集的沉积物中热原和成岩多环芳烃的富集在空间上表现为生物(或天然)多环芳烃的混合或稀释。

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