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台湾新大港及邻近沿海地区沉积物中多环芳烃的分布与来源识别

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

作者信息

Fang Meng-Der, Lee Chon-Lin, Yu Chia-Shun

机构信息

Department of Marine Environment and Engineering, National Sun Yat-sen University, Kaohsiung, Taiwan, ROC.

出版信息

Mar Pollut Bull. 2003 Aug;46(8):941-53. doi: 10.1016/S0025-326X(03)00099-7.

DOI:10.1016/S0025-326X(03)00099-7
PMID:12907187
Abstract

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 ( summation operator 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-dimethylphenanthrene (4,6-C(2)D/3,6-C(2)P) 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(2)D/3,6-C(2)P, PER/ summation operator PAH (perylene to summation operator 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.

摘要

对新打港及其邻近沿海地区的33个沉积物样本进行了气相色谱-质谱联用(GC-MS)分析,以测定多环芳烃(PAHs)的含量。所分析的30种母体和烷基化多环芳烃(ΣPAH)的总浓度在98.1至3382纳克/克干重之间变化。内港站点的甲基菲/菲(MP/P)值大于2,同时菲/蒽(P/A)值非常低,这表明低分子量多环芳烃的很大一部分可能来自石油污染源,具体而言,是废机油的非法处置。研究发现,4,6-二甲基二苯并噻吩/3,6-二甲基菲(4,6-C₂D/3,6-C₂P)比值在追踪从内港区到邻近沿海环境的石油源多环芳烃方面比MP/P比值更有用。此外,根据层次聚类分析,采集的沉积物聚为三大类:近海组、近岸组和内港组。在本研究中,代表石油源、生物源和热解源的三个诊断比值,即4,6-C₂D/3,6-C₂P、苝/ΣPAH(苝与ΣPAH)和苯并(a)蒽/ Chrysene(苯并(a)蒽/ Chrysene),被发现可有效区分和表征各组沉积物。所采集沉积物中热解源和石油源多环芳烃的富集在空间上表现为被生物源(或天然)多环芳烃混合或稀释。

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