珠江澳门河口沉积物柱样中有机氯农药的垂直分布特征

以GC/ECD内标法定量测定了沉积物柱样品中有机氯农药含量 ,以便探讨柱样中有机氯农药的垂直变化特征及可能的来源 .样品采自珠江澳门河口 ,柱样以2 10 Pb同位素法定年 .定量测定结果表明以BHCs、DDTs总量计算时 ,样品中含量分别为 0 4 8～ 2 6 2 8ng/ g、1 92～ 39 1 3ng/ g .柱样中农药含量随深度变化和珠江口区的水域水流量随年份的变化有着很好的对应性 .有机氯农药主要是来源于施用农药长期风化后的土壤 .样品中DDTs的浓度超过了河口沉积物化学品风险评价最低值标准 .     

无锡鼋头渚夜鹭卵中有机氯农药残留及其环境指示意义

分析了太湖鼋头渚夜鹭卵中的有机氯农药残留情况,发现在禁用近20年后,HCH的异构体、DDT及其代谢物、异狄氏剂以及环氧七氯在夜鹭卵中都不有同程度的检出,其中β－HCH和p,p‘-DDE的残留水平和检出率均很高,p,p‘-DDE平均达到了0.906ug/g(干重）。研究发现无锡夜鹭卵中多数有机氯农药残留水平平均高于江西共青城地区的样品。无锡夜鹭卵孵化率较低。可能与DDE残留量较高有关。夜鹭卵中有机氯农药残留水平具有指示环境污染的意义。     

聚合硫酸铁混凝消除水中有机氯的研究

采用聚合硫酸铁(PFS)絮凝剂对水中有机氯农药(OCPs)进行强化混凝处理,并运用响应曲面法(RSM)优化分析了影响OCPs去除率的混凝条件,如pH值、原水浊度、混凝剂投加量和OCPs的初始浓度诸因素.结果表明,各影响因素交互作用显著,最佳混凝条件组合为:pH=5.0、原水浊度=150NTU、PFS投加量为12mg/L、OCPs初始浓度为200ng/L,在此条件下,PFS絮凝剂可有效去除水中OCPs,经模型验证实验得到最佳条件下去除率α-HCH为82.23%、β-HCH为71.15%、γ-HCH为77.28%、δ-HCH为86.27%、 p,p’-DDE为93.78%,与RSM预测值基本相同.结合絮体分形维数和Zeta电位对混凝效果的机理进行了探讨,表明各因素均达到了最佳水平.     

Characteristics and risk assessment of organochlorine pesticide residues in surface sediments collected at the Qingshitan Reservoir

ABSTRACT

An ultrasonic extraction – gas chromatography – electron capture detector analytical method was used to measure the concentration and types of organochlorine (OC) pesticides in sediment to obtain a better understanding of the characteristics and hidden ecological risks associated with OC pesticide exposure in surface sediment of the Qingshitan Reservoir. Fifteen types of OC pesticides were detected in the sediment, and the sum concentration of these chemicals was in the 149.32–490.19 ng/g range (mean value: 319.39 ng/g). The concentrations of detected OC pesticides occurred in the following order: hexachlorohexanes (HCHs) (mean value: 200.17 ng/g) > DDTs (mean value: 36.92 ng/g) > heptachlors (mean value: 32.74 ng/g) > methoxychlor (mean value: 24.13 ng/g). There was a 100% detection rate for HCH isomers, and their concentrations occurred in the following order: β-HCH > δ-HCH > γ-HCH > α-HCH. β-HCH was the main component of HCHs. Ratios between α-HCH/γ-HCH and β-/(α+γ)-HCH were used to investigate the sources of pollution. Most of the surveyed areas were polluted by lindane, which originated from past pesticide residue usage, and no new inputs of HCHs were found. DDT was the major component of the DDTs, and accounted for 52%–87% of the DDTs. The ratios of (DDE+DDD)/DDT at all sample collection points were less than 1, indicating that degradation rate of DDTs in sediment was low and there was a new input of DDTs in these surveyed areas. The ratio of DDD/DDE was less than 1 at most of the sample collection points, indicating that the degradation of DDT in the sediments primarily took place under aerobic conditions. Comparison of OC pesticide residual levels in the underwater sediment collected at the Qingshitan Reservoir to other states and countries showed the pollution level of these chemicals of the Qingshitan Reservoir was relatively high. The ecological risk was assessed based on guideline values of effects range-low (ERL) and effects range-medium (ERM). The results showed that DDD, DDE, DDTs and endrin residues in the sediment posed a moderate ecological risk, but DDT and γ-HCH showed high ecological risk. These OC pesticides might adversely affect biological systems, and need to be addressed.     

Distribution of persistent organochlorine pesticides in tissue/organ of silver carp (Hypophthalmichthys molitrix) from Guanting Reservoir, China

The concentration of organochlorine pesticides（OCPs） in tissues and organs of silver carp（Hypophthalmichthys mofitrix） from Guanting Reservoir were investigated to evaluate the pollution potential and distribution of OCPs. A total of 16 OCPs were measured and the concentrations were in the range of 1.61-69.01 ng/g wet weight（ww） for total OCPs, 0.16- 0.75 ng/g ww for HCB. 0.75 -26.80 ng/g ww for SHCH（sum of α-,β-, γ- and δ-HCH） and 0.68-35.94 ng/g ww for SDDT（ sum of p, p＇-DDE, p, p＇-DDD, o, p＇-DDT and p, p＇- DDT）. The mean concentrations of total OCPs, HCB, ∑HCH, and ∑DDT were 18.04, 0.96, 7.14 and 9.28 ng/g ww, respectively. Among the organochlorine pesticides, β-HCH and p, p＇-DDE were the most dominant compounds in tissue and organ with the average concentrations of 4.42 and 8.14 ng/g, respectively. The results obtained in this study show that the levels of 16 OCP residues found in silver carps are low and pose no threat to human health and wildlife fed upon them on the basis of existing related quality guidelines. However, recent input of lindane and DDT might still exist in the area investigated and further investigation should be carried on.     

活性炭纤维萃取浓缩水样中微量有机磷农药

采用活性炭纤维(ACF)为固相萃取剂填料,萃取测定水样中微量有机磷农药。研究分析了ACF用量、洗脱剂类型、农药初始质量浓度、水样过柱速度及pH等因素对萃取回收率的影响。结果表明:洗脱剂类型和ACF用量是显著的影响因素。最佳萃取条件为:含0 1μg L有机磷农药的1L加标水样,需0 2gACF和8mL二氯甲烷,水样过柱速度40mL min。pH对萃取影响不大。萃取回收率为80 7%～118%。      

蔬菜中有机磷农药残留的生物传感器法检测

将乙酰胆碱酯酶(AChE)固定在醋酸纤维膜上,将该膜组装在一支pH玻璃电极敏感膜表面,制成用于测定有机磷农药的电位型生物传感器,优化其制备方法。当溶液中存在有机磷农药,酶的活性受到抑制,酶活性的降低引起pH玻璃电极电位的改变,其改变程度与溶液中农药的浓度大小有关。用本文方法测定了蔬菜中的对硫磷、辛硫磷、氧乐果、敌敌畏,结果满意。     

珠江三角洲河口及邻近海区沉积物中含氯有机污染物的分布特征

对采自珠江三角洲河口及其邻近海区的表层沉积物样品中含氯有机污染物多氯联苯和有机氯农药进行了定量分析测定,并探讨了其在珠江三角洲地区的分布特征．结果表明,沉积物已受到了一定程度的污染,其中澳门内港和广州河段的样品已经受到严重的有机氯污染.从有机氯农药来看,其分布为澳门内港＞澳门南环湾＞珠江广州河段＞狮子洋＞伶仃洋＞西江;多氯联苯的分布为广州芳村＞澳门内港＞珠江广州河段＞狮子洋＞伶仃洋≈西江．     

Organochlorine pesticides in the ambient air of Chiapas, Mexico

Organochlorine (OC) pesticides were measured in the ambient air of Chiapas, Mexico during 2000-2001. Concentrations of some OC pesticides (DDTs, chlordanes, toxaphene) were elevated compared with levels in the Great Lakes region, while those of other pesticides were not (hexachlorocyclohexanes, dieldrin). While this suggests southern Mexico as a source region for the former group of chemicals, comparably high levels have also been reported in parts of the southern United States, where their suspected sources are soil emissions (DDTs, toxaphene) and termiticide usage (chlordane). Ratios of p,p'-DDT/p,p'-DDE and trans-chlordane/cis-chlordane/trans-nonachlor (TC/CC/TN) in Chiapas suggest a mixture of fresh and weathered sources, while congener profiles of toxaphene suggest emission of old residues from soils. This is supported by air parcel back trajectory analysis, which indicated that air masses over Chiapas at the time of sampling had previously passed over areas of continuing or recent use of some OC pesticides as well as areas of past use.     

Concentration and fate of persistent organochlorine pesticides in estuarine sediments using headspace solid-phase microextraction

The concentration and fate of persistent organochlorine pesticides (OCPs) in estuarine surface sediments in Erh-jen and Lan-yang rivers, Taiwan were investigated using headspace solid-phase microextraction (HSSPME) method to evaluate the possible pollution potential and guideline for OCP concentrations in Taiwan. The HSSPME method exhibits a good analytical performance with low detection limits for OCP determination in sediment. In addition, results obtained using the developed HSSPME method were in good agreement with those obtained using Soxhlet extraction in a certified sample. The developed analytical method was further applied to the determination of concentrations of OCP residues in surface sediments from the estuaries of the selected rivers in Taiwan. A total of 20 surface sediments from each river was collected from 10 sampling stations. The total OCP concentrations in sediments from Erh-jen River ranged from 0.17 to 5.04 ng/g-dw with the mean values of 0.25–1.24 ng/g-dw for HCHs, 0.10–0.89 ng/g-dw for cyclodienes and 0.16–0.64 ng/g-dw for DDTs. The concentrations of OCPs in sediments from Lan-yang River were in the range 0.37–0.9 ng/g-dw with an average of lower than 0.5 ng/g-dw. HCHs and DDTs were abundant in the estuarine sediments from the selected rivers. Results obtained in this study show that the origin of OCPs in the surface sediments from Erh-jen River is a combination of erosion of the weathered soils and long-range atmospheric transport, while the OCP concentrations found in Lan-yang River could be regarded as the background levels of OCPs in Taiwan.