哈密地区环境中^220Rn子体α潜能浓度所致居民剂量估算

用ＳｔｒａｎｄｅｎＥ．推荐的测量方法对哈密地区环境空气中２２０Ｒｎ子体α潜能浓度测量结果表明，室内、外平均值分别为５６．１和１０．２（×１０－７Ｊ·ｍ－３）。室内外２２０Ｒｎ／２２２Ｒｎ子体α潜能浓度比值分别为０．８４和０３２。２２０Ｒｎ子体所致居民有效剂量当量为２２８μＳｖ·ａ－１（集体有效剂量当量为０．９×０２ｍａｎ·Ｓｖ）。     

内蒙古某灌域表层土壤六氯环己烷空间分布特征及影响因素

为修复灌区内土壤有机氯农药污染，降低六氯环己烷对土壤环境的危害，对内蒙古某灌域表层土壤进行采样，利用气相色谱测定50个土壤样品中六氯环己烷及其异构体的含量，并利用ArcGIS空间分析技术确定表层土壤中六氯环己烷的分布状况。样本中六氯环己烷的检出率为96%，各样本中六氯环己烷的浓度范围为未检出~23.0 ng/g，平均浓度为4.4 ng/g。4种异构体含量平均值顺序为γ-六氯环己烷>δ-六氯环己烷>β-六氯环己烷>α-六氯环己烷。灌域东北部和西南部残留浓度较高，并由这2个方向向中部地区逐渐递减，表层土壤中的六氯环己烷分布受土壤黏粒量、不同种植种类和灌溉水源的影响较大。虽受人类耕作的影响，但表层土壤中的六氯环己烷污染水平相对较低。     

车载巡测在区域射频电磁环境质量监测与表征中的应用分析

对北京中央电视塔周围25 km²区域电磁环境质量分别进行了射频的网格法手工监测和车载巡测自动监测，通过SPSS软件等对两种监测方法获取的数据进行了统计对比分析，发现两组数据在总体水平及数值分布特征上较为接近，因此车载巡测监测可以替代网格法监测。以车载巡测数据为基础，绘制了实测数据的道路电磁地图，利用插值法绘制了区域电磁地图，对区域电磁环境质量进行了直观表征。从回应公众关注和城市电磁规划出发，建议今后可利用车载巡测监测加强时域和频域的监测。     

潜水含水层水位观测孔水位伪变化的观测与分析

结合CIRP试验场包气带的介质结构及渗透性特征，在S9孔进行了短期的孔中水位、孔口气压和温度测量，测量结果表明，观测孔水位波动与大气压变化有关，水位波动具有伪变化。水位伪变化对于试验场潜水位的监测有一定影响，因此，应对带有伪变化的水位观测结果进行必要的修正，以反映潜水位的真实动态。     

基于网格空间数据的晋陕蒙接壤区生态环境综合评价

晋陕蒙接壤区是典型的生态过渡带、生态脆弱带。文章在调查研究的基础上 ,选取了 1 3个评价指标 ,应用层次分析法确定其权重 ,并将各个因子分级标准化和定量赋值 ,再用加权求和法得到每个评价单元的环境质量综合评价指数。根据环境综合评价指数将环境质量分为较好 (≥ 8)、一般 (≥ 6～ <8)、较差 (≥ 4～ <6)、恶劣 (<4) 4级。结果表明 :晋陕蒙接壤区的环境质量大多处于较差等级 ,较好、一般、较差、恶劣等级的面积比例分别为 2 .2 % ,2 8% ,5 7.4%和1 2 .4%     

夜间建筑施工噪声扰民监测方法探讨

以一家夜间施工工地为例 ,通过对现有夜间建筑施工噪声测量方法及国家和深圳经济特区有关噪声污染定义的分析 ,阐述了夜间施工工地噪声扰民监测方法     

萃取-催化氧化光度法测定生物体中H2O2含量研究

提出萃取-催化氧化光度法测定生物体中H2O2含量的新方法.用稀土催化H2O2产生羟基自由基以氧化二苯基碳酰二肼,生成红色二苯基碳酰腙,其最大吸收波长为563.0nm;当二苯基碳酰二肼浓度一定时,△A563与H2O2含量呈量效关系.在0～30μmol/L H2O2 含量范围内,该法能简单、快速、精确地测定生物样品中H2O2实际含量.     

灰色模型在确定关键污染因子中的应用

将灰色模型引入水环境质量评价中 ,通过对某个时间段内污染物原始监测数据的灰色处理 ,从动态演变中找出关键因子 ,客观地判定各污染因子所起的作用 ,并对各因子在下一个时间段的发展趋势作出判断 ,增加了评价的准确性。经过实例运用分析表明 ,该方法物理意义明确 ,简便易用     

Atrazine and Alachlor Inputs to Surface and Ground Waters in Irrigated Corn Cultivation Areas of Castilla-Leon Region, Spain

The inputs of atrazine and alachlor herbicides to surface and ground waters from irrigated areas dedicated to corn cultivation in the Castilla-León (C-L) region (Spain) as related to the application of both herbicides were studied. Enzyme-linked immunosorbent assays (ELISA) were used for monitoring the atrazine and alachlor concentrations in 98 water samples taken from these areas. Seventy-nine of the samples were of ground waters and 19 were of surface waters. The concentration ranges of the herbicides detected in the study period (October 1997–October 1998) were 0.04–25.3 g L^–1 in the surface waters and 0.04–3.45 g L^–1 in the ground waters for atrazine, and 0.06–31.9 g L^–1 in the surface waters and 0.05–4.85 g L^–1 in the ground waters in the case of alachlor. The highly significant correlation observed between the concentrations of both herbicides in the surface waters (r = 0.89, p < 0.001) pointed to a parallel transport of atrazine and alachlor to these waters. A study was made of the temporal evolution of the concentrations of both herbicides, and it was found a maximum recharge of atrazine in the ground waters for April 1998 and of alachlor in October 1997 and October 1998. The temporal evolution of the concentrations of both herbicides in surface waters was parallel. The highly significant correlations observed between atrazine concentrations determined by ELISA and by HPLC (r = 0.92, p < 0.001) and between alachlor concentrations also determined by both methods (r = 0.96, p < 0.001) confirmed the usefulness of ELISA for monitoring both herbicides in an elevated number of samples. Using HPLC, the presence in some waters of the alachlor ethanesulfonate (ESA) metabolite was found at a concentration range of 0.52–4.01 g L^–1. However the interference of ESA in the determination of alachlor by ELISA was negligible. The inputs of atrazine and alachlor to waters found in this study, especially the inputs to ground waters, could pose a risk for human health considering that some waters, though sporadically, are even used for human consumption.