中国东南沿海的地质构造特征

本文主要论述了中国东南大地构造演化特征。晋宁旋回,南北板块碰撞,形成近东西向构造格局、转换块间带及交结盆地。加里东旋回至印支旋回,东南地壳由非成熟性地壳逐渐向稳定性大陆地壳过渡。陆壳的生长是以两个外隆为中心呈环带状向外扩张。燕山旋回,大陆破坏和改造,形成大陆边缘的流纹岩链。显示了地壳生长为多旋回前进演化的特征。     

基于[火用]分析法的矿区工业生态链物质能量流动研究

从工业生态学角度研究矿区工业生态系统的工业代谢和工业生态链，建立矿区物质循环与能量流动[火用]分析和[火用]效率模型。根据生态效率的理念，矿区发展需要五项关键支撑技术，为合理选择煤炭的产业链延伸途径打下理论基础，促进矿区可持续发展。     

内蒙古东部地区电力工业用水对策及可持续发展研究

合理进行水资源配置，是当前确保各个行业用水的关键；在工业生产和建设中保护好环境和自然生态，从而保证工业的可持续发展，是整个社会发展非常重要的一环：本文宏观地提出了针对内蒙古东部地区电力工业用水的对策及可持续发展研究的建议。     

二十一世纪大型炼油厂给排水系统节水设计

分析了我国炼油厂环境污染存在的问题，提出了21世纪炼油厂给排水系统节水的具体措施。     

Verification of carrier status for Becker muscular dystrophy from analysis of a blighted ovum

The polymerase chain reaction (PCR) was used on material from a blighted ovum to confirm indirectly the carrier status of a woman with a family history of Becker muscular dystrophy. Conventional testing including creatine kinase levels, muscle biopsy, and EMG had been inconclusive, and on the basis of one elevated creatine kinase level, the woman had been designated a possible carrier. Ultrasound examination at 10 weeks of pregnancy indicated a blighted ovum, from which DNA was subsequently extracted and subjected to PCR testing for determination of sex and genotypic status with respect to the known familial deletion of the dystrophin gene. The blighted ovum was found to have a Y chromosome and also to be deleted for at least exon 6 of the dystrophin gene, indirectly indicating that the mother most likely carried the family mutation for Becker muscular dystrophy.     

山东省森林资源与木材供需平衡模型的建立与应用

本文在对山东省森林资源和木材供需平衡状况进行系统分析的基础上，利用系统动力学方法建立了山东省森林资源与木材供需平衡模型，通过对不同方案的政策仿真和结果分析，试图提出解决山东省木材供需矛盾的最佳途径，为制定林业发展政策提供依据。     

高强铝合金超塑挤压成形

主要介绍了工业牌号高强铝合金在供应态或经简单预处理后在通用油压机上超塑成形的实例,并分析探讨了非理想组织材料超塑成形中微观组织的变化。     

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.     

宁夏人口、粮食与水土资源利用

人口、粮食与水土资源利用是宁夏回族自治区国民经济发展中的重要问题。文中分析了宁夏人口、粮食与水土资源利用现状,应用灰色系统理论及回归分析,建立人口、粮食预测模型,对2000年宁夏的人口、粮食进行了预测。分析2000年水土资源不同开发利用条件下粮食供需平衡情况后指出,充分合理利用黄河水资源,扩大灌溉面积,配合先进的农业技术,宁夏粮食不仅能自给,而且还能提供一定数量的商品粮。最后提出了解决粮食问题,防止生态环境恶化的主要途径。     

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.