Lancaster Environment Centre, Lancaster University, Lancaster, LA1 4YQ, UK.
Environ Sci Pollut Res Int. 2012 Jul;19(6):1953-62. doi: 10.1007/s11356-012-0944-7. Epub 2012 Jul 6.
Concentrations of selected organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) are reported in air and surface soil in an extensive spatial survey across Azerbaijan, a country bordering the Caspian Sea with a history of OCP production and extensive use. Polyurethane foam disc passive air samplers (PAS) were deployed during October-November 2008 with soil samples collected in July 2009. Levels of Σ(7)PCB in ambient air were generally low (mean of 0.046 ng m(-3), n = 13) and comparable to concentrations reported in countries within Eastern Europe and similar to or lower than concentrations reported in urban air in the UK and other western countries. Surprisingly, PCB concentrations in rural/background soil fell below the method detection limits at most sites, although concentrations were 0.209 and 0.071 ng Σ(7)PCB g(-1) dry weight (dw) for two urban sites, again comparable to PCB levels measured at background sites in Europe. Levels of α-HCH, β-HCH, γ-HCH and p,p'-DDT/E were elevated in ambient air across Azerbaijan in comparison to PAS-derived concentrations reported elsewhere, with concentrations of α-HCH in air ranging from 0.085 to 2.699 ng m(-3) and p,p'-DDE, 0.037-2.290 ng m(-3). High concentrations of OCPs occurred at several of the urban sites and at sites in proximity to old pesticide storage facilities with concentrations in soil >0.1 μg g(-1) dw for p,p'-DDE and p,p'-DDT at several sites. The ratio of p,p'-DDT/p,p'-DDE was close to unity in the soil at these sites, but elsewhere, the ratio was <1, indicating a weathered DDT pattern, which was also reflected in the air at all sites. A fugacity approach revealed the strong likelihood of net soil-to-air transfer at the majority of sites for all OCPs. The calculated annual fluxes or loading to the atmosphere from a rural/agricultural area (representing land as vineyards and cotton cultivation) were estimated to be on the order of ≈10-100 kg year(-1) for the HCH isomers (including the β -isomer) and p,p'-DDE. The high levels of OCPs in soils, particularly in the vicinity of obsolete-pesticide storage facilities and at select urban sites are of concern and warrant regular monitoring activities and the development of containment or mitigation strategies.
在阿塞拜疆进行了广泛的空间调查,报告了空气中和地表土壤中选定的有机氯农药 (OCPs) 和多氯联苯 (PCBs) 的浓度。该调查在 2008 年 10 月至 11 月期间使用聚氨酯泡沫盘被动空气采样器 (PAS) 进行,并于 2009 年 7 月采集土壤样本。环境空气中Σ(7)PCB 的水平通常较低(平均值为 0.046 ng m(-3),n = 13),与东欧国家报告的浓度相当,与英国和其他西方国家城市空气中的浓度相似或更低。令人惊讶的是,尽管在两个城市地点,土壤中Σ(7)PCB 的浓度为 0.209 和 0.071 ng Σ(7)PCB g(-1) 干重 (dw),但大多数农村/背景地点的 PCB 浓度都低于方法检测限,这与欧洲背景地点测量的 PCB 水平相当。与其他地方 PAS 衍生浓度相比,阿塞拜疆空气中的α-HCH、β-HCH、γ-HCH 和 p,p'-DDT/E 浓度升高,空气中的α-HCH 浓度范围为 0.085-2.699 ng m(-3),p,p'-DDE,0.037-2.290 ng m(-3)。在几个城市地点和靠近旧农药储存设施的地点,OCPs 浓度较高,在几个地点,土壤中 p,p'-DDE 和 p,p'-DDT 的浓度>0.1 μg g(-1) dw。在这些地点的土壤中,p,p'-DDT/p,p'-DDE 的比值接近 1,但在其他地方,比值<1,表明 DDT 风化模式,这也反映在所有地点的空气中。逸度方法表明,在大多数地点,所有 OCPs 的土壤向空气的净转移极有可能发生。从一个农村/农业地区(代表葡萄园和棉花种植)估算的每年通量或向大气的负荷估计为 HCH 异构体(包括β-异构体)和 p,p'-DDE 的约 10-100 kg 年(-1)。土壤中 OCPs 水平较高,特别是在废弃农药储存设施附近和一些城市地点,令人关注,需要开展定期监测活动,并制定遏制或缓解策略。