加强工业污染防治 实现环保全面达标

对燕化公司开展环保全面达标工作做了综述和总结，几年的综合污染防治工作证明，加强环保管理、持续推行清洁生产和较先进的污染治理技术促进了燕化公司经济和生产的发展，同时降低了废物排放，取得了明显的效果。     

依靠安全科技搞好安全生产

对搞好安全生产必须依靠安全科技进行了论述.提出了在安全工作中必须运用科技手段的必要性和必须正视的几个现实问题.     

DNA polymorphism and globin chain analysis in the prenatal diagnosis of β-thalassaemia major in Taiwan

Thirty-six pregnancies in 25 families at risk of β-thalassaemia major received prenatal diagnosis. Chorionic villus sampling or amniocentesis was done in 35 pregnancies to obtain fetal cells for DNA linkage study, for which Southern blotting and DNA hybridization were used to detect seven restriction fragment length polymorphisms (RFLPs) within the β-globin gene cluster: ϵ-HincII, ^Gγ-HindIII, ^Aγ-HindIII, Φβ-HincII, 3′Φβ-HincII, β-AvaII, and 3′β BarnHI. β-Thalassaemia major was diagnosed in seven and excluded in 22 pregnancies. In the remaining six cases, β-thalassaemia major could not be excluded. In these six pregnancies and another one with late booking, ultrasound-guided cordocentesis was performed at the 22nd to 27th week of gestation. Globin chain composition was determined with urea-acetic acid-Triton X-100-12 per cent polyacrylamide gel electrophoresis. β-Thalassaemia major was diagnosed in two fetuses and excluded in the other five. Eleven fetuses (in which β-thalassaemia major was excluded) have been delivered and are healthy at more than 5 months old DNA linkage analysis coupled with globin chain electrophoresis provides an effective way for prenatal diagnosis of β-thalassaemia major, although these methods are being replaced by more direct detection techniques using oligonucleotide probes.     

水产品加工废水生物处理现状与展望

介绍了几种较为典型的水产品加工废水生物处理工艺,以及利用生物处理工艺处理高含盐量废水实验室研究结果;展望了水产品加工废水处理技术的发展前景。     

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.     

两种共生模式之比较

在对两种共生模式—生态工业园和绿色供应链作了基本解释和案例分析后，比较了这两种模式的共性和异性，得出了它们在生态工业体系建设中具有统一性和互补性的结论，对建设城市生态工业体系提出了看法。     

Prenatal diagnosis for dystrophia myotonica using the polymerase chain reaction

The polymerase chain reaction has been used to detect an abundant class of short repeat DNA families of the form (dC-dA)n.(dG-dT)n, known as microsatellites. These units are found throughout the human genome and have been characterized for several loci including APOC2 on chromosome 19ql2-ql3.2. The locus APOC2 is linked to the gene for dystrophia myotonica and a microsatellite within this locus was used to derive polymorphisms in a family to predict the inheritance of the disease. Chorionic villus sampling (CVS) was performed at 151/2 weeks' gestation. Following DNA extraction from the CVS material and parental blood samples, microsatellite analysis was carried out by the polymerase chain reaction.     

Prenatal diagnosis of β-thalassaemia in Mediterranean populations by dot blot analysis with DNA amplification and allele specific oligonucleotide probes

In this study, we describe a simple strategy to detect β-thalassaemia mutations in prospective parents and to make prenatal diagnosis in pregnancies at risk in the Mediterranean population. Screening of prospective parents is carried out by dot blot analysis on enzymatically amplified DNA with a set of oligonucleotide probes complementary to the most common mutations in this population. Prenatal diagnosis is accomplished by the same procedure on enzymatically amplified amniocyte or trophoblast DNA. The main advantages of this procedure are the simplicity, sensitivity (0.05 μg of DNA), and rapidity (12–24 h). Further simplification is obtained by amplification of the DNA from crude amniotic cell lysate. The very low amount of fetal material necessary for this analysis eliminates the need to culture amniotic fluid cells and may decrease the fetal loss rate associated with trophoblast sampling. The number of specific DNA sequences obtained by the amplification procedure allowed us to use non-radioactive labelled oligonucleotide probes, which have several advantages compared to radioactive probes.     

皮革和毛皮加工废水处理技术

采用混凝沉淀-酸化水解-悬挂链曝气-生物接触氧化组合工艺处理皮革和毛皮加工生产废水。实验结果表明;进水COD为2400mg/L,处理后出水COD≤100mg/L,去除率≥95.8%。各项水质指标均稳定地达到了GB8978-96污水综合排放一级标准。     

中山市金属回收企业绿色供应链绩效评价研究

废旧金属资源的回收是循环经济的重要组成部分,进一步加强废旧金属回收行业的管理,对于保证资源永续、减少环境污染、节省能源、提高经济效益具有重要的意义。当前的竞争环境使金属回收企业和政府主管部门急需通过金属回收企业绿色供应链绩效评价,了解企业的绿色供应链管理状况,以适应越来越激烈的市场竞争。因而建立一个金属回收企业绿色供应链绩效评价模型不仅对绿色供应链的实践具有指导意义,而且还能对金属回收企业绿色供应链的绩效作出评价,改善其绿色供应链管理。