水环境数学模型在河流水质管理规划中的应用

本文讨论了水环境数学模型的选择及在水质管理规划中的使用方法,达到实用的目的.具有广泛的通用性和实用性.     

关于模糊数学在环境质量综合评判中“最大隶属度”原则不适用性的讨论

通过对模糊数学在环境质量综合评判中的分析，指出“最大隶属度”原则的不适用性，并根据环境质量分级所存在的固有关系提出改进的方法。     

铁路运输业污水治理系统分析

研究了乌鲁木剂铁路局系统污水治理污染控制方法及途径，提出了主要污染物为石油类，其最佳治理对策是：确定重点污染单位、污染源、用最低的治理投入，选择斜板隔油气浮工艺治理重点污染和次重点污染部门，得到较好的治理效果，否定盲目追求“零排放”的高投入方案。     

合成洗涤剂对小鼠诱变性研究

连续５天腹腔注射同一剂量（１／５ＬＤ５０）的合成洗涤剂，取小鼠骨髓细胞测定嗜多染色红细胞的微核率，研究表明，３种合成洗涤剂（加大香洗衣粉，洁牌餐具洗涤剂，恩威高级餐具洗洁精）使小鼠微核率有所增高，但恩威，洁牌餐具洗涤剂与对照无显著性差异。     

Euclidean贴近度水质评价法及其应用

分析了模糊综合评判在水质评价中的缺陷,将模糊数学中的贴近度与经典的Euclidean距离结合,提出Euclidean贴近度水质评价法。结果表明,该评价方法具有科学性、合理性,并且精度高,简单实用。     

应用模糊综合指数法对伊犁河（伊宁段）水质的综合评价

模糊数学法对伊犁河(伊宁段)水质进行综合评价时,由于分别采用地面水环境质量标准中五类标准值的平均值及其中三个标准值,计算后的结果不一致,而模糊综合指数法避免了这类问题的出现,计算结果比较满意.从而表明,该法是对模糊数学法的进一步改进.     

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。     

乌伦古湖水质现状及污染防治对策

着重对乌伦古湖所监测的项目作了全面系统的分析，评价了该湖的水环境质量，指出乌伦古湖水质的主要问题是严重咸化，这是该湖可持续发展的最大障碍。并指出做好湖区规划，增加水源供给，加强污水处理和湿地建设，是乌伦古湖未来发展的有利措施。     

An Assessment on Variation of Sulphur Dioxide and Particulate Matter in Erzurum (Turkey)

Sulphur dioxide and PM₁₀ levels are investigated in Erzurum during the periods of 1990–2000 heating season to assess air pollution level. For that reason, emissions of sulphur dioxide and particulate matter were calculated by using consumption of fuels and Turkish emission factors. These emission values were evaluated together with air pollution levels, which were measured at six stations in Erzurum atmosphere during 1990–2000 winter periods. Results reveal that in 1990–1994 heating period, there is an increasing trend in the emissions and air pollution levels over Erzurum, and the air quality limits were not met. The daily 24 h limit (short-term limit) was exceeded 127 days in 1992–1993 winter period. The reason for this increase was found to be the switching to use of low-quality fossil fuels instead of cleaner ones. Results also indicated that there was a considerable decrease in emissions of air pollutants and air pollution levels after 1995. This can be explained by the consumption of more high-quality fossil fuels. The correlation coefficient of SO₂ with PM₁₀ is obtained as r² = 0.85, which is a high value supporting the idea that both pollutants are emitted from the same source.     

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.