中国乌鲁木齐土壤中有机氯的来源、组成与风险评价

Twenty-eight surface soil samples from 5 functional zones (park, traffic roadside, business/residential area, rural area, and industrial area) of Ürümqi, China were collected and analyzed for the concentrations of 14 organochlorine pesticides (OCPs), such as 3 isomers of hexachlorocyclohexane (HCHs) (α-HCH, β-HCH, and γ-HCH), 4 dichlorodiphenyltrichloroethanes (DDTs) (p, p’-DDT and its metabolites p, p’-DDD (1,1-dichloro-2,2-bis(p-chlorophenyl)ethane) and p, p’-DDE (1,1-dichloro-2,2-bis(4-chorophenyl)ethylene), and o, p’-DDT), and methoxychlor, aiming to survey the residue levels and compositions of these 14 OCPs, to identify possible sources of the OCPs, and to assess their potential risks to human health and the environment in surface soils of Ürümqi. The concentrations ranged from non-detected to 30.86 μg kg^-1 for HCHs (sum of α-, β-, and γ-HCH), from non-detected to 40.03 μg kg^-1 for DDTs (sum of p, p’-DDT, p, p’-DDD, p, p’-DDE, and o, p’-DDT), and from non-detected to 11.95 μg kg^-1 for methoxychlor. The total concentrations of the OCPs ranged from 16.40 to 84.86 μg kg^-1, with a mean of 41.89 ± 16.25 μg kg^-1. According to the measured concentrations and occurrence rates of the 14 OCPs, DDTs, HCHs, and methoxychlor were the most dominant compounds. Among the 5 functional zones, the total concentration of OCPs was in the order of rural area > traffic roadside > park > business/residential area > industrial area. The different compositions of DDTs and HCHs indicated that the residues of these compounds in most soil samples originated from historical application, besides slight recent introduction at some sampling sites. The results of Pearson correlation analysis showed that soil total organic carbon played an important role in the residue levels of HCHs, but such relationships were not found with DDTs or other OCPs. The soil quality of Ürümqi was classified as Class I based on the guidelines of the Chinese Environmental Quality Standard for Soil (GB15618-1995), indicating that the residue levels of OCPs have little risks to the environment and human health in the study area.     

有机溶剂对有机氯农药污染场地土壤淋洗修复效用研究

Problems associated with organochlorine pesticide (OCP)-contaminated sites in China have received wide attention. To solve such problems, innovative ex-situ methods of site remediation are urgently needed. We investigated the feasibility of the extraction method with different organic solvents, ethanol, 1-propanol, and three fractions of petroleum ether, using a soil collected from Wujiang (WJ), China, a region with long-term contamination of dichlorodiphenyltrichloroethanes (DDTs). We evaluated different influential factors, including organic solvent concentration, washing time, mixing speed, solution-to-soil ratio, and washing temperature, on the removal of DDTs from the WJ soil. A set of relatively better parameters were selected for extraction with 100 mL L 1 petroleum ether (60-90℃): washing time of 180 min, mixing speed of 100 r min 1 , solution-to-soil ratio of 10:1, and washing temperature of 50℃. These selected parameters were also applied on three other seriously OCP-polluted soils. Results demonstrated their broad-spectrum effectiveness and excellent OCP extraction performance on the contaminated soils with different characteristics.     

Remediation of Organochlorine Pesticide-Contaminated Soils by Surfactant-Enhanced Washing Combined with Activated Carbon Selective Adsorption

Remediation of organochlorine pesticide (OCP)-contaminated soils is urgently required especially in China. The present study investigated the removal of OCPs from two soils by triton X-100 (TX-100)-enhanced washing coupled with powdered activated carbon (PAC) adsorption treatment of the solution. Two contaminated soils, including a silt clay contaminated with chlordene, 1,1-dichloro-2,2-bis(p-chlorophenyl)ethanes (DDDs), and dichlorodiphenyltrichloroethane (DDT) and a sandy loam containing chlordanes and mirex, were selected. Effects of varied operating parameters, including TX-100 dosage, liquid/soil (L/S) ratio, and extraction time, on the contaminant removal were examined. For both soils, OCP removal was clearly enhanced with increasing TX-100 in extraction solution and L/S ratio. Meanwhile, the removal efficacy was also impacted by soil texture and characteristics and contents of the contaminants. Moreover, by using PAC as an absorbent, a significant decrease in the contaminants in the extraction solutions was detected, and TX-100 could be further reused. Our investigation suggests that surfactant-enhanced washing combined with activated carbon selective adsorption would be an alternative to remediate OCP-contaminated soils.     

运用红边参数估算叶片叶绿素含量

Soil samples collected from several sites along an altitudinal transect on the eastern slope of the Tibetan Plateau were analyzed for hexachlorobenzenes(HCHs) and dichlorodiphenyltrichloroethanes(DDTs).The results showed that HCHs and DDTs were found in the soil samples from the remote high altitude areas away from source regions,which confirmed the long-range atmospheric transport phenomenon of these organochlorine pesticides(OCPs) insecticides.The OCP concentrations in the soils had a significant negative correlation with altitude;they showed a trend to increase with decreasing altitude,but the increase was not continuous,being interrupted at some moderate-altitude sites on the transect.The distances from the source region,landforms,soil properties,and physical-chemical properties of OCPs were more important than total organic carbon content to the distribution of OCPs in soils disturbed by human activities.An analysis of the compositions of HCH isomers and DDTs revealed predominantly low ratios of α-HCH to γ-HCH,ranging from 0.06 to 4.79,which suggested current lindane inputs.On the other hand,low p,p-DDT/p,p-DDE and o,p-DDT/p,p-DDT ratios were observed,indicating mainly aged historical DDT residues in the study area.     

花鸟岛贻贝养殖区六六六、滴滴涕和多氯联苯的赋存及健康风险评价

为了探究长江口贻贝养殖区不同介质（水体、土壤与贻贝）中传统持久性有机污染物（POPs）的浓度、组成、介质间分布特征,使用气相质谱联用仪（GC-MS/MS）对水体、土壤和贻贝样品中的六六六（HCHs）、滴滴涕（DDTs）和多氯联苯（PCBs）含量进行测定分析。研究表明：传统POPs在样品中广泛检出,HCHs、DDTs和PCBs在贻贝中含量分别为10.8~49.1、169~900和10.4~34.4 ng/g（脂重）,在水体中0.22~1.76、0.07~0.29 ng/L和9.45~51.8 pg/L,在土壤中0.18~10.4、2.62~69.6和0.40~0.69 ng/g (干质量)。DDTs是贻贝中主要的污染化合物。养殖区水体和土壤中目标化合物组成反映其受到污染排放残留影响,贻贝中高氯联苯和滴滴涕降解产物占主导地位,符合生物积累特征。土壤中HCHs、DDTs和PCBs存在很多显著正相关,贻贝同样,这反应了污染物可能存在相似的来源,在主成分分析中可以看出贻贝组织与非生物介质间的关系。健康风险评价表明,人群摄食长江口贻贝几乎不会引起接触风险和致癌风险。本研究可为了解贻贝养殖区传统POPs在介质中的归趋,及人群食用贻贝提供依据。