Level of coordinated development in economy and environment

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处理含锌铅钢铁厂粉尘的Inmetco工艺

Ｉｎｍｅｔｃｏ工艺是处理含锌铅钢铁厂粉尘的重要方法。本文在实验的基础上，对该工艺处理我国含锌铅钢铁厂粉尘的可行性和合理性作了论述。     

政策环境影响评价与公众参与——国家有毒化学品立法EIA中的公众参与

阐明在我国开展政策EIA的必要性,从可持续发展的角度探讨政策EIA中公众参与的目的、意义、方法和特点,并介绍和分析国家有毒化学品立法EIA开始阶段中的公众参与。     

光合细菌与酵母跨界融合(杂合)子发酵味精废水研究

光合细菌球形红假单胞菌（Ｒｈｏｄｏｐｓｅｕｄｏｍｏｎａｓ ｓｐｈａｅｒｏｉｄｅｓ）酿酒酵母（Ｓａｃｃｈａｒｏｍｙｃｅｓ ｃｅｒｅｖｉｓｉａｅ）细胞分别经溶菌酶和蜗牛酶脱壁形成原生质体，在聚乙二醇（ＰＥＧ）和Ｃａ＾２＋诱导下实现了真核与原核细胞的超远缘杂交，经抗菌素培养基初步鉴定，融合产物能同时在含有链霉素和制霉菌素的培养基中生长，而双亲细胞只能在含有单一抗菌素的培养基中生长，经初筛与得获得高絮弟性     

污水处理场改造中浮选工艺单元的优化

浮选工艺在国内是比较成熟的工艺，但是更先进的工艺技术在待进一步的开发和利用，借我厂污水场改扩之机，从理论上论证隐厂所选用的先进而独特的工艺技术--一级浮选采用生化出水分流的方式，此种方法能耗最低，去除率最高，值得推广和应用。     

Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in a family with a previous fatal case of sudden unexpected death in childhood

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is a potentially fatal inherited disease with a carrier frequency of approximately 1:100 in most Caucasian populations. The disease is implicated in sudden unexpected death in childhood. A prevalent disease-causing point mutation (A985G) in the MCAD gene has been characterized, thus rendering diagnosis easy in the majority of cases. Since the clinical spectrum of MCAD deficiency ranges from death in the first days of life to an asymptomatic life, there are probably other genetic factors—in addition to MCAD mutations—involved in the expression of the disease. Thus, families who have experienced the death of a child from MCAD deficiency might have an increased risk of a seriously affected subsequent child. In such a family we have therefore performed a prenatal diagnosis on a chorionic villus sample by a highly specific and sensitive polymerase chain reaction (PCR) assay for the G985 mutation. The analysis was positive and resulted in abortion. We verified the diagnosis by direct analysis on blood spots and other tissue material from the aborted fetus and from family members.