Equipe Physico-chimie de l'atmosphère, UMR 7515 CNRS Institut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé (ICPEES), Université de Strasbourg, Strasbourg, France.
Laboratoire des Matériaux, Catalyse, Environnement et Méthodes Analytiques (LMCEMA), Ecole doctorale des sciences et technologies, Hadath, Beirut, Lebanon.
Environ Sci Pollut Res Int. 2015 Nov;22(22):17850-9. doi: 10.1007/s11356-015-5030-5. Epub 2015 Jul 12.
In this study, pine needles were used as cost-effective and reliable passive bio-monitors to concomitantly evaluate atmospheric concentrations of three classes of persistent organic pollutants, polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), and polycyclic aromatic hydrocarbons (PAHs). The extraction of persistent organic pollutants (POPs) from needle samples was performed. Eleven PCBs, 11 OCPs, and 15 PAHs were detected and followed through time in needle samples from three sites in the Strasbourg region. The urban and rural sites were more exposed to PCBs than the suburban site. The highest concentration of PCBs was found at the urban site, but the largest number of congeners (10) was detected at the rural site. PCB 189 and 156 were the predominant congeners in the rural site and PCB 70 in the urban site. For OCPs, the rural site displayed the highest concentrations (up to 22.9 ng g(-1)) and number of compounds investigated (9). The high concentration of γ- and β-hexachlorocyclohexane (HCH) at that time in the urban site was the reason for this result. γ- and β-HCH were the two predominant compounds in all samples. The suburban and urban sites were the most exposed with PAHs with pyrene, phenanthrene, and acenaphthene being the three predominant compounds in these sites. No specific trend in terms of time was apparent for PCBs and OCPs. However, higher concentrations were detected for some compounds in the first sampling, especially for PAHs, and this is attributed to variations in meteorological conditions (e.g., temperature, wind, rain) and variable inputs from both identified and unidentified sources.
在这项研究中,我们使用松针作为具有成本效益和可靠的被动生物监测器,同时评估三类持久性有机污染物,即多氯联苯(PCBs)、有机氯农药(OCPs)和多环芳烃(PAHs)在大气中的浓度。从针状样本中提取持久性有机污染物(POPs)。在斯特拉斯堡地区的三个地点的针状样本中,我们检测到并跟踪了 11 种 PCBs、11 种 OCPs 和 15 种 PAHs 的时间变化。城市和农村地区的 PCBs 暴露水平高于郊区。在城市地区发现了最高浓度的 PCBs,但在农村地区发现了最多数量的同系物(10 种)。在农村地区,PCB189 和 PCB156 是主要的同系物,而在城市地区,PCB70 是主要的同系物。对于 OCPs,农村地区显示出最高的浓度(高达 22.9ng/g)和所调查化合物的数量(9 种)。当时城市地区γ-和β-六氯环己烷(HCH)的高浓度是造成这种结果的原因。γ-和β-HCH 是所有样品中两种主要的化合物。郊区和城市地区受到 PAHs 的影响最大,其中苊、荧蒽和苊烯是这些地区的三种主要化合物。在 PCBs 和 OCPs 方面,没有明显的时间趋势。然而,在第一次采样中,一些化合物的浓度更高,特别是 PAHs,这归因于气象条件(如温度、风和降雨)的变化以及来自已识别和未识别来源的可变输入。