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被动采样为纽瓦克湾是美国纽约/新泽西地区大气中多氯二苯并对二恶英和呋喃的来源提供了证据。

Passive sampling provides evidence for Newark Bay as a source of polychlorinated dibenzo-p-dioxins and furans to the New York/New Jersey, USA, atmosphere.

机构信息

University of Rhode Island Graduate School of Oceanography, Narragansett, Rhode Island, USA.

出版信息

Environ Toxicol Chem. 2012 Feb;31(2):253-61. doi: 10.1002/etc.742. Epub 2011 Dec 14.

DOI:10.1002/etc.742
PMID:22095897
Abstract

Freely dissolved and gas phase polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) were measured in the water column and atmosphere at five locations within Newark Bay (New Jersey, USA) from May 2008 to August 2009 with polyethylene (PE) passive samplers. Mono- to octa-CDDs and mono- to hepta-CDFs were detected in bottom and surface waters at ≤ 20 pg/L with no clear gradient between sampling locations, suggesting freely dissolved PCDD/Fs are well mixed in Newark Bay. The most concentrated, freely dissolved gas phase congener was 2,7/2,8-dichlorodibenzo-p-dioxin (2,7/2,8-DiCDD), likely originating from photochemical conversion of triclosan in Newark Bay. Air-surface water gradients strongly favored net volatilization of PCDD/PCDFs from Newark Bay. Water-to-air fluxes of 2,7/2,8-DiCDD and 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD), the most concentrated and the most toxic PCDD/PCDFs, respectively, were approximately 60 ng/m(2) per month and 14 to 51 pg/m(2) per month. Significant decreases in freely dissolved 2,3,7,8-TCDD concentrations with increasing freshwater near the Passaic River and conservative behavior during the summer of 2009 suggested Passaic sediments as a likely source of 2,3,7,8-TCDD to Newark Bay. Mass balance calculations implied that almost 50% of freely dissolved 2,3,7,8-TCDD delivered to Newark Bay from the Hackensack and Passaic Rivers was lost to volatilization in the summer of 2009.

摘要

2008 年 5 月至 2009 年 8 月,利用聚乙烯(PE)被动采样器在纽瓦克湾(美国新泽西州)的五个地点测量了水柱和大气中的游离溶解态多氯二苯并对二恶英(PCDDs)和多氯二苯并呋喃(PCDFs)。在底部和表层水中检测到单氯至八氯二苯并对二恶英和单氯至七氯二苯并呋喃,各采样点之间没有明显的梯度,表明自由溶解的 PCDD/Fs 在纽瓦克湾中充分混合。最集中的自由溶解气相同系物是 2,7/2,8-二氯二苯并对二恶英(2,7/2,8-DiCDD),可能源自纽瓦克湾中三氯生的光化学转化。空气-水梯度强烈有利于纽瓦克湾中 PCDD/PCDFs 的净挥发。2,7/2,8-DiCDD 和 2,3,7,8-四氯二苯并对二恶英(2,3,7,8-TCDD)的水-气通量(分别为最集中和最有毒的 PCDD/PCDFs)约为每月 60ng/m(2)和 14 至 51pg/m(2)。随着靠近帕塞伊克河的淡水比例增加,自由溶解态 2,3,7,8-TCDD 浓度显著降低,2009 年夏季保守行为表明帕塞伊克沉积物可能是纽瓦克湾 2,3,7,8-TCDD 的一个潜在来源。质量平衡计算表明,2009 年夏季从哈肯萨克河和帕塞伊克河输送到纽瓦克湾的自由溶解态 2,3,7,8-TCDD 有近 50%因挥发而损失。

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