东太湖渔业发展对水环境的影响及其生态对策

东太湖网围养殖始于1984．至今养殖面积达3200hm^2。占东太湖面积的24％以上。网围养殖的盲目发展带来了湖泊的水质污染．沼泽化等环境问题。为保护东太湖水域环境。必须明确湖泊功能定位。减少湖泊污染源。并在此基础上进行人工调控．合理放养。完善湖泊生态系统结构。针对东太湖水生植被退化的趋势。应恢复和加强对优质水生植被的保护。促进湖泊生物多样性。恢复其良性生态。     

斯德哥尔摩,人类环保之船从这里启航

1969年。经由瑞典政府提议．联合国大会决定1972年在瑞典首都斯德哥尔摩召开联合国人类环境会议。这是联合国历史上首次以环保为主题的会议．是人类环境意识觉醒的标志．在人类社会发展史上具有里程碑式的意义。1972年6月5日，会议在斯德哥尔摩隆重开幕。133个国家的1300多名代表出席了这次会议。会议通过了《联合国人类环境会议宣言》和《行动计划》。宣告了人类环境新观念的诞生，达成了“只有一个地球”．人类与环境是不可分割的“共同体”的共识。1972年6月5日。全球环境保护的航船从斯德哥尔摩启航。33年过去了，让我们重回斯德哥尔摩，去寻找历史的轨迹．去了解这座环保之都的未来航向。[编者按]     

PHBV表面疏水改性用作吸油材料的研究

利用多种表面改性剂对生物可降解材料PHBV进行了表面改性实验研究，测定了不同改性剂改性后PHBV的吸油率以及温度对其吸油效果的影响，并探讨了改性机理，研究结果表明：不同改性剂对PHBV的改性效果有所差异，从疏水和吸油的共同效果来看，最佳疏水改性剂为添加量5％时的硅油，温度对未改性PHBV和改性PHBV的吸油率及吸油速度均有影响。     

中水回用工程投建与运行实践

沈阳理工大学学生城中水设施的建设，不仅提高了水资源的重复利用率，创造良好的环境效益和经济效益，同时也为中水回用工作的推广实施积累了经验。尤其是采用比较简单的污水处理工艺达到中水回用的标准，其中最主要的部分是沉淀和生物接触氧化以及最后的过滤和消毒，这样的工艺比较适合中等规模的投资，从回用水的经济效益上看这样的中水回用系统还是比较适合推广。     

贵州水城青山铅锌矿床地球化学研究

通过对青山铅锌矿床矿石矿物、蚀变围岩、含矿层、辉绿岩的稀土元素、硫、碳、氧同位素及黔西北岩石地层中铅锌含量的研究，笔者认为，成矿金属并非源于岩浆岩，而源于深部的沉积岩，碳、硫分别源于碳酸盐岩和含矿地层的硫酸盐硫；大气降水经深循环再上升形成成矿介质水。     

地铁环境振动预测方法浅析

简要介绍了国内外关于地铁环境振动预测方法的研究概况,在作者研究分析地铁振动传播途径和主要影响参数基础上,给出了简单定量预测地铁环境振动程度之方法,应用该方法所得到的预测值,与现场实测值误差在±2dB范围内.     

Trisomy 7 in chorionic villi: Follow-up studies of pregnancy,normal child,and placental clonal anomalies

Cytogenetic study of chorionic villi sampled because of advanced maternal age revealed, after overnight culture, an apparently non-mosaic trisomy 7. Amniocentesis showed exclusively normal mitoses, and the pregnancy continued normally. One hundred mitoses from cord blood of the normal newborn revealed a non-mosaic 46,XX complement. No cells with a proven trisomy 7 were found in cultures from either of two biopsies of the morphologically normal placenta, but the peripheral biopsy showed in multiple cultures an abnormal clone: 47,XX, + 20,-2,-21, + t(2;21)(p13;q22). To our knowledge, this is the first case of non-mosaic trisomy 7 detected on CVS which has had follow-up studies of amniotic fluid, cord blood, and term placenta.     

Attitudes of women of childbearing age towards prenatal diagnosis in Southeastern France

The objective of this study was to explore women's attitudes towards prenatal diagnosis of trisomy 21 and to examine some of the factors possibly responsible for these attitudes before implementing in real practice serological screening of pregnant women at risk for trisomy 21. We carried out a telephone survey on a representative sample of women who had recently had a normal livebirth delivery in the Marseille district in 1990. The participation rate was 80 per cent and the average age of the mothers was 28-9 years. Among the 514 women interviewed, 78 per cent stated that they would ask for an amniocentesis for a 1 per cent risk of trisomy 21 at their next pregnancy. When adjusting for confounding factors, the decision to have or not to have an amniocentesis was found to depend not only on the women's attitude towards induced abortion, but also on their understanding of the risk involved and on the social context (knowing a handicapped child, discussion with the father). It also depended on the women's age and on what they knew about amniocentesis from the medical point of view. The risk of miscarriage can influence a woman's choice but this objection was not found to affect the women's decisions significantly in our survey. The data showed the existence of a high potential demand for fetal karyotyping.     

Nature and frequency of chromosomal abnormalities in pregnancies with abnormal ultrasound findings: An analysis of 117 cases with review of the literature

During a 7-year period, 117 fetal karyotypes were available from 131 genetic amniocenteses. These procedures were performed between 14 and 37 weeks' gestation for the following abnormal ultrasound findings: (1) intrauterine growth retardation (IUGR)—61 cases; (2) fetal malformation—71 cases; and (3) amniotic fluid volume (AFV) abnormality—60 cases. Chromosomal abnormalities were identified in 19 cases (16.2 per cent). Aneuploidy was 2.5 times as frequent in the presence of malformations than in their absence. No correlation was demonstrated between specific fetal malformations and specific chromosomal abnormalities. Aneuploidy was also twice as frequent in the presence of symmetrical IUGR than in its absence. No chromosomal abnormalities were found among eight cases of asymmetrical IUGR. Four cases of aneuploidy presented with isolated IUGR, three of these involving the X chromosome. The frequency of aneuploidy was the same with or without abnormalities of AFV (14.3 versus 16.4 per cent). No chromosomal abnormality was found associated with isolated AFV abnormalities.