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大气中更高水平的黑碳和喜马拉雅山较小地区土壤-空气分配中有机氯的贡献。

Higher atmospheric levels and contribution of black carbon in soil-air partitioning of organochlorines in Lesser Himalaya.

机构信息

Department of Environmental Sciences, Quaid-i-Azam University, Islamabad 45320, Pakistan.

Centre for Chemicals Management, Lancaster Environment Centre, Lancaster University, Bailrigg, Lancaster LA1 4YQ, UK.

出版信息

Chemosphere. 2018 Jan;191:787-798. doi: 10.1016/j.chemosphere.2017.10.021. Epub 2017 Oct 4.

Abstract

Due to influence of wind patterns (monsoon and westerlies) and anthropogenic activities, lower stretch of Himalaya is at direct exposure to persistent organic pollutants (POPs). Current study was designed to monitor atmospheric concentrations of long lived organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) using polyurethane passive air sampling in the Lesser Himalayan Region (LHR) of Pakistan. Levels of ∑HCHs, ∑DDTs and ∑PCBs were observed in a range between 3 and 210 pg m, 0.75-67.1 pg m and 8.49-458 pg m, respectively. Though, air mass trajectories over LHR indicated long range transport as atmospheric source input which was further explained by Clausius-Clapeyron plots between ln P and inverse of temperature (1000/T; K) where all OCPs and most of the PCBs have shown insignificant relationship (r = 5E-06-0.41; p-value = 0.06-0.995). However, local source emissions and valley transport may also implicate based on spatial distribution and altitudinal patterns. Additionally, soil-air partitioning of organochlorines was assessed using octanol-air partition (K) and black carbon-air partition (K) based models. Regression results indicated combined influence of both organic matter (r = 0.298-0.85) and black carbon (r = 0.31-0.86) via absorption and adsorption, respectively in soil-air partitioning of OCs in LHR. This paper sheds light on the atmospheric concentrations of OCs and help in better understanding of the processes involved in fate and transport of organic pollutants in Himalayan region. Further investigations are required to understand the role of carbon moieties in fate and transport of other groups of organic pollutants at higher altitudes of Himalayan region.

摘要

由于风型(季风和西风)和人为活动的影响,喜马拉雅山的下游地区直接暴露在持久性有机污染物(POPs)之下。本研究旨在利用聚氨酯被动空气采样监测巴基斯坦小喜马拉雅地区(LHR)大气中长寿命有机氯农药(OCPs)和多氯联苯(PCBs)的浓度。∑HCHs、∑DDTs 和∑PCBs 的浓度范围分别为 3 至 210 pg/m、0.75 至 67.1 pg/m 和 8.49 至 458 pg/m。然而,LHR 上空的气团轨迹表明,大气源输入是长程传输,克劳修斯-克拉佩龙图(ln P 与温度倒数(1000/T;K)之间的关系)进一步解释了这一点,其中所有 OCPs 和大多数 PCB 都显示出无显著关系(r=5E-06-0.41;p 值=0.06-0.995)。然而,根据空间分布和海拔模式,本地源排放和山谷传输也可能存在。此外,还利用辛醇-空气分配(K)和黑碳-空气分配(K)模型评估了有机氯在土壤-空气之间的分配。回归结果表明,在 LHR 中,有机污染物在土壤-空气之间的分配受有机物(r=0.298-0.85)和黑碳(r=0.31-0.86)的综合影响,分别通过吸收和吸附。本文重点介绍了 OC 在大气中的浓度,并有助于更好地了解喜马拉雅地区有机污染物的归宿和传输过程。需要进一步的研究来了解碳成分在喜马拉雅地区更高海拔地区其他有机污染物归宿和传输过程中的作用。

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