南水北调中线不同调水方案下的汉江水华发生概率分析

为评估南水北调中线工程对汉江中下游水华的影响，从汉江水华的成因机理分析入手，提出了汉江水华发生概率的计算模型．该模型由河流一维水动力学模型、水体富营养化模型以及随机数生成模型组成，它不仅可以模拟汉江水华的发生机理，而且可以对诱发水华的各种因子进行随机抽样组合，从而求出中线调水不同方案实施后汉江水华的发生概率．计算结果表明，在现状情况下汉江水华的发生概率为9．2％，南水北调中线各调水方案（无引江济汉工程）实施后，汉江水华发生的概率将有一定程度的增加，而如果调水方案与引江济汉工程同时兴建将大大减少汉江水华发生的概率．最后提出建议，汉江自身的水污染治理是减少水华发生概率的最根本措施，而丹江口水库和引江济汉工程的联合调度将会减小汉江水华发生的概率．     

Degradation of nitrobenzene in aqueous solution by ozone-ceramic honeycomb

IntroductionAs a promising advanced oxidation technology for watertreatment ,catalytic ozonation has received great attentionforthe efficient degradation of organic compoundsinrecent years(Legube , 1999) . Some studies showed that homogeneousand heterogen…     

上海合流污水深海排放强化一级预处理的研究

复合式厌氧污泥床反应器是一种改进的厌氧处理工艺 ,可有效去除城市生活污水中的污染物 ,并提高了污水的可生化性 ,是一种较理想的城市污水强化一级处理工艺 ,为上海合流污水深海排放的实施提供了保障。本文对该工艺的装置特点和处理效果进行了分析研究 ,并对其应用前景进行了展望。     

天津地区表层土壤多环芳烃含量的中尺度空间结构特征

应用地统计学技术对全天津地区表层土壤中 16种优控多环芳烃含量和土壤理化参数进行了空间结构分析 .结果显示 ,各组分浓度均存在中尺度的空间自相关性 .多环芳烃浓度的空间结构存在明显的各向异性 .大气运移和土壤TOC含量可能是影响土壤多环芳烃浓度空间结构特征的重要环境因素 .     

高强度开发区域生态环境规划研究——以上海市宝山区生态环境规划为例

通过对区域生态环境-经济协调性现状的诊断,指出上海宝山区产业结构和空间布局的不合理是造成该区域环境污染严重的主要原因。规划从可持续发展的思路出发,形成合理的产业结构调整方案,利用环境功能区划引导区内产业结构和布局调整,构建面向高强度开发区域的生态环境指标体系,最终提出针对产业特点及环境现状的生态环境规划方案。     

开式冷挤压成形深小锥孔件时极限变形程度的理论研究

给出了深小锥孔件开式冷挤压成形时极限变形程度的定义,建立了变形区非稳态连续速度场;利用上限原理得到了极限变形程度的理论判据。分析了各主要参数对极限变形程度的影响规律,对指导制定深小锥孔件开式冷挤压成形工艺具有重要意义。     

两种方法监测近岸大气NOX浓度的比较

分别用常规法和离子色谱法对近岸海域大气ＮＯＸ 进行同步监测，并对两方法间的相关性和测定结果的换算进行了研究。结果表明： 两者呈极显著的正相关，相关系数达０－８３５（ｎ＝ ９） ，其测定结果是可换算的。为此，建立了采用离子色谱法测定气溶胶ＮＯ－３ 浓度预测近岸大气ＮＯＸ 浓度的方法。     

JHX新型浮选机在处理含油污水中的应用

介绍JHX新型高效射流浮选机在处理含油污水中的应用，考察各种工艺条件下JHX浮选机的工作情况，JHX浮选机由于其独特的发泡原理和结构设计，对含油污水有很高的除油效率。     

Detection of fetal HLA-DQα sequences in maternal blood: A gender-independent technique of fetal cell identification

The objective of this study was to detect fetal HLA-DQα gene sequences in maternal blood. HLA-DQα genotypes of 70 pregnant women and their partners were determined for type A1. We specifically sought couples where the father, but not the mother, had genotype A1. In 12 women, maternal blood samples were flow-sorted. Candidate fetal cells were isolated and amplified by using PCR primers specific for a paternal HLA-DQα A1 allele. Fetal HLA-DQα A1 genotype was predicted from sorted cells; amniocytes or cheek swabs were used for confirmation. Six of twelve sorted samples had amplification products indicating the presence of the HLA-DQα A1 allele; 6/12 did not. Prediction of the fetal genotype was 100 per cent correct, as determined by subsequent amplification of amniocytes or cheek swabs. We conclude that paternally inherited uniquely fetal HLA-DQα gene sequences can be identified in maternal blood. This system permits the identification of fetal cells independent of fetal gender, and has the potential for non-invasive prenatal diagnosis of paternally inherited conditions.     

DNA-based carrier detection and prenatal diagnosis of tyrosinase-negative oculocutaneous albinism (OCA1A)

We describe molecular prenatal diagnosis and carrier detection of tyrosinase-negative oculocutaneous albinism (OCA1A) in two families. In one family, we carried out DNA-based prenatal diagnosis of OCA1A. In the other family, mutation analysis and carrier detection obviated the need for prenatal diagnosis. Molecular analysis is safer and probably more accurate than fetoscopy and fetal scalp biopsy, and should become the method of first choice for prenatal diagnosis of OCA1.