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Field testing of equilibrium passive samplers to determine freely dissolved native polycyclic aromatic hydrocarbon concentrations.用于测定自由溶解态天然多环芳烃浓度的平衡被动采样器的现场测试。
Environ Toxicol Chem. 2008 Mar;27(3):499-508. doi: 10.1897/07-253.1.
2
Greatly reduced bioavailability and toxicity of polycyclic aromatic hydrocarbons to Hyalella azteca in sediments from manufactured-gas plant sites.在人造煤气厂场地沉积物中,多环芳烃对阿氏摇蚊的生物可利用性和毒性大幅降低。
Environ Toxicol Chem. 2007 Jun;26(6):1146-57. doi: 10.1897/06-207r.1.
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Temporal bioavailability of organochlorine pesticides and PCBs.有机氯农药和多氯联苯的时间生物利用度。
Environ Sci Technol. 2006 Jun 15;40(12):3689-95. doi: 10.1021/es052427h.
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Ecological risk assessment of polycyclic aromatic hydrocarbons in sediments: identifying sources and ecological hazard.沉积物中多环芳烃的生态风险评估:识别来源与生态危害
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Annual variation of polycyclic aromatic hydrocarbon concentrations in precipitation collected near the Great Lakes.五大湖附近采集的降水中多环芳烃浓度的年变化。
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Sources of heavy metals and polycyclic aromatic hydrocarbons in urban stormwater runoff.城市雨水径流中重金属和多环芳烃的来源。
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Comparative evaluation of background anthropogenic hydrocarbons in surficial sediments from nine urban waterways.九条城市水道表层沉积物中背景人为源碳氢化合物的比较评估
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Atmospheric deposition of polycyclic aromatic hydrocarbons to Atlantic Canada: geographic and temporal distributions and trends 1980-2001.多环芳烃在加拿大大西洋地区的大气沉降:1980 - 2001年的地理和时间分布及趋势
Environ Sci Technol. 2004 Apr 1;38(7):1941-8. doi: 10.1021/es034645l.

一条正在进行超级基金修复的城市河流中自由溶解的多环芳烃的时空变化。

Spatial and temporal variation of freely dissolved polycyclic aromatic hydrocarbons in an urban river undergoing Superfund remediation.

作者信息

Sower Gregory James, Anderson Kim A

机构信息

Environmental and Molecular Toxicology Department, Oregon State University, Corvallis, Oregon 97331, USA.

出版信息

Environ Sci Technol. 2008 Dec 15;42(24):9065-71. doi: 10.1021/es801286z.

DOI:10.1021/es801286z
PMID:19174872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4172327/
Abstract

Urban rivers with a history of industrial use can exhibit spatial and temporal variations in contaminant concentrations that may significantly affect risk evaluations and even the assessment of remediation efforts. Concentrations of 15 biologically available priority pollutant polycyclic aromatic hydrocarbons (PAHs) were measured over five years along 18.5 miles of the lower Willamette River using passive sampling devices and HPLC. The study area includes the Portland Harbor Superfund megasite with several PAH sources including remediation operations for coal tar at RM 6.3 west and an additional Superfund site, McCormick and Baxter, at RM 7 east consisting largely of creosote contamination. Study results show that organoclay capping at the McCormick and Baxter Superfund Site reduced PAHs from a precap average of 440 +/- 422 ng/L to 8 +/- 3 ng/L postcapping. Results also reveal that dredging of submerged coal tar nearly tripled nearby freely dissolved PAH concentrations. For apportioning sources, fluoranthene/pyrene and phenanthrene/anthracene diagnostic ratios from passive sampling devices were established for creosote and coal tar contamination and compared to published sediment values.

摘要

具有工业使用历史的城市河流可能会出现污染物浓度的时空变化,这可能会显著影响风险评估,甚至影响修复工作的评估。使用被动采样装置和高效液相色谱法,在五年时间里沿着威拉米特河下游18.5英里的区域对15种生物可利用的优先污染物多环芳烃(PAHs)的浓度进行了测量。研究区域包括波特兰港超级基金大型场地,有多个多环芳烃来源,包括西部6.3英里处煤焦油的修复作业,以及东部7英里处的另一个超级基金场地麦考密克和巴克斯特场地,该场地主要受杂酚油污染。研究结果表明,麦考密克和巴克斯特超级基金场地的有机粘土覆盖将多环芳烃浓度从覆盖前的平均440±422纳克/升降至覆盖后的8±3纳克/升。结果还显示,疏浚水下煤焦油使附近自由溶解的多环芳烃浓度几乎增加了两倍。为了确定来源,针对杂酚油和煤焦油污染,建立了被动采样装置中荧蒽/芘和菲/蒽的诊断比率,并与已发表的沉积物值进行了比较。