The Status of Pesticide Residues in the Drinking Water Sources in Meiliangwan Bay, Taihu Lake of China

The study was carried out to assess the levels of pesticide residues in the water of Meiliangwan Bay, Taihu Lake of China. The most commonly employed organochlorine pesticides (OCPs), organophosphorus pesticides (OPPs) and herbicide atrazine were analyzed. The water samples were collected seasonally from Meiliangwan Bay within a period of one year. The pesticides were analyzed by gas chromatography (GC) with μECD or NPD after solid-phase extraction (SPE), which was confirmed by GC with an ion trap mass spectrometry (MS). The mean concentrations were 1.98 ng/l for lindane, 0.378 ng/l for heptachlor epoxide, 0.367 ng/l for p,p′-DDE, 0.496 ng/l for p,p′-DDD, 1.06 ng/l for p,p′-DDT and 51.6 ng/l for dichlorvos, 39.0 ng/l for demeton, 346 ng/l for dimethoate, 4.12 ng/l for methyl parathion, 11.6 ng/l for malathion, 2.17 ng/l for parathion and 217 ng/l for atrazine. Generally, low concentrations of OCP were found, whereas the concentrations of the OPPs and atrazine in the water of Taihu Lake were relatively high. Heptachlor epoxide and lindane were the two most commonly encountered OCPs while dichlorvos, demeton and dimethoate were found to have much higher concentrations and occurrences than other OPPs.  

U PLC- ESI- MS/MS法同时测定水中7种抗生素

采用超高效液相色谱-电喷雾二级质谱联用技术同时测定水中7种抗生素,优化了试验条件.磺胺甲恶唑、诺氟沙星、环丙沙星、氧氟沙星、四环素在1.00 ng/L～1000 ng/L范围内线性良好,定量下限为1 ng/L,土霉素、金霉素在10.0 ng/L-2 000 ng/L范围内线性良好,定量下限为10 ng/L,去离子水和地表水样加标回收率为72.1%-112%,RSD为0.6%～9.2%.  

网格监测统计积分模式的推导与应用

把大气污染物的空间分布看成是连续变化的超曲面,采用积分法推导网格监测点位均值的积分模式,并由此推导监测范围内污染物总量模式。利用丹东市环境空气SO2被动扩散网格监测数据,采用此模式计算其趋势值和均值。  

Characteristics of CO2 release from forest soil in the mountains near Beijing

CO₂ release from forest soil is a key driver of carbon cycling between the soil and atmosphere ecosystem. The rate of CO₂ released from soil was measured in three forest stands (in the mountainous region near Beijing, China) by the alkaline absorption method from 2004 to 2006. The rate of CO₂ released did not differ among the three stands. The CO₂ release rate ranged from ??341 to 1,193 mg m^???2 h^???1, and the mean value over all three forests and sampling times was 286 mg m^???2 h^???1. CO₂ release was positively correlated with soil water content and the soil temperature. Diurnally, CO₂ release was higher in the day than at night. Seasonally, CO₂ release was highest in early autumn and lowest in winter; in winter, negative values of CO₂ release suggested that CO₂ was absorbed by soil.  

土壤中6种氯代多环芳烃测定方法的建立及应用

建立了加速溶剂萃取、凝胶渗透色谱（GPC）与气相色谱-质谱联用测定土壤中6种氯代多环芳烃的分析方法。研究证实该法的最佳萃取条件为：10.34 MPa压力,100 ℃萃取温度下，以1∶1（V/V）的正己烷/二氯甲烷为萃取溶剂，静态萃取10 min，循环4次。GPC净化过程用乙酸乙酯和环己烷的混合液1∶1（V/V）做洗脱液，目标物的收集时间为25~35min。方法对Cl-PAHs在1~500 μg/L范围内线性良好，相关系数R²为0.998 4~0.999 7；LOD和LOQ分别为2.6~25.1 pg/g和8.7~83.6 pg/g；各目标物的低浓度回收率为64.1%~117.6%，RSD<12.05%；高浓度回收率为59.1%~105.3%，RSD<9.81%。研究证实该法满足定量分析的要求，并应用该法对某化工园进行了氯代多环芳烃的检测。  

水样发光细菌急性毒性测试的方式与表征

选取不同类型的环境和污染源水样开展了发光细菌毒性测试,针对不同环境管理目标,探讨了急性毒性定量表征方式.发光细菌急性毒性测试在环境应急监测、水源早期生物预警中,采用绘制毒性预警基线图的方式比较可行.在污染源监督监测中,对于发光抑制率低于60%、无法求出EC50的样品,采用等效毒性参照物的质量浓度表征废水的毒性;对于发光抑制率高于60%,采用稀释因子表示样品的毒性更直观可靠.  

电子垃圾回收地得克隆的污染水平及分布特征

对浙江某电子垃圾回收地水体、沉积物、土壤以及大气中得克隆（DP）的污染水平及分布特征进行了调查。结果表明，水、沉积物、土壤和大气样品中均检测出了 DP，分别为0．843～1．56 ng/L，0．185～7．03 ng/g干重，0．115～26．4 ng/g干重和11．2 pg/m3；该区域 DP分布特征表明电子垃圾的拆解和焚烧是环境中 DP的重要来源。  

自制固相微萃取涂层用于自来水中五氯酚的测定

采用石英毛细管作为模具,甲基丙烯酸和乙二醇二甲基丙烯酸酯在石英纤维表面原位聚合得到聚(甲基丙烯酸-乙二醇二甲基丙烯酸酯)作为固相微萃取涂层,并以五氯酚为研究对象,采用顶空SPME-GC-ECD法对该涂层的萃取性能进行评价。使用正交试验优化萃取温度、萃取时间、盐浓度、pH和搅拌速度。在最优条件下,建立了水样中五氯酚的分析方法,方法检出限为1ng/L,线性范围为2～5000ng/L,线性相关系数为0.9999,相对标准偏差(RSD,n=5)为8.9%,加标回收率为110.8%。  

室内空气中的气态多环芳烃的被动采样监测

利用自制被动采样装置,在2011年秋冬季对南京市部分地区室内空气中5种气态多环芳烃(PAHs)(萘、苊烯、苊、芴、菲)进行了为期100d的连续采样检测,被动采样器的采样速率为0.012m3/d,5种PAHs的回收率在63%～105%之间,方法检出限在1.1～2.4ng范围内。结果表明,南京市5处不同室内环境空气中萘的浓度最高,占总量的90%以上。室内环境空气中5种PAHs的总浓度为230～1564ng/m3。住宅内人体对5种PAHs的暴露速率为479～560ng/h。