1000t/d含油废水旋流分离技术及设备研究

将实验室研制的 HL 型旋流器用压力容器式方式并联起来 ,建立 10 0 0 t/ d规模的示范装置 ,并进行试验。示范装置的试验结果表明 ,与工业测试比较 ,HL型旋流器并没有因为规模的放大而造成性能下降 ,它能取代石化行业目前采用的“一隔二浮”流程中的大部分装置 ,具有明显的经济效益和广阔的应用前景     

Detecting neural tube defects by amniocentesis between 11 and 15 weeks' gestation

Forty-two open neural tube defects (NTDs) were identified in our series of 7440 amniocenteses tested between 11 and 15 weeks of gestation. Using a cut-off of ≥2.0 MOM, the detection rate for open NTDs was 95 per cent; 100 per cent each for anencephaly and spina bifida; and 78 per cent for encephalocele. Two encephaloceles had AFP levels less than 2.0 MOM and negative AChEs. Thirty-four (81 per cent) of these NTDs were tested between 13 and 15 weeks and 8 (19 per cent) before 13 weeks. There were 0.6 per cent false positives by AFP (excluding serious abnormalities and fetal death) and 0.1 per cent after AChE. The likelihood of an open NTD after an elevated AFP (≥2.0 MOM) was 24 and 77 per cent for any serious abnormality. These results, when combined with an earlier study, indicate that amniotic fluid AFP appears to be as sensitive a test for open NTDs between 13 and 15 weeks as between 16 and 20 weeks. Additional experience is necessary to determine this before 13 weeks.     

华南玄武岩红土化过程中微量元素地球化学

广东、海南的玄武岩．在强烈的红土化过程中．元素在红土剖面中发生迁移和残留、贫化和富集。根据红土化过程中元素的地球化学性状，将元素划分为活泼元素和不活泼元素两大类。并首次采用了元素它集因子这个概念来探讨红土化过程中微量元素的地球化学行为。最后讨论了红土化过程小金的表生富集作用。     

The importance of chorionic villus sampling after first trimester diagnosis of cystic hygroma

The prenatal diagnosis of The Turner Syndrome is described at a menstrual age of 12 weeks. Detection of cystic hygroma was followed by vaginal chorionic villous sampling (CVS) which revealed a 45,X karyotype. Early documentation of fetal karyotype in the presence of a cystic hygroma is essential for accurate diagnosis and genetic counselling.     

Molecular cytogenetic characterization of marker chromosomes found at prenatal diagnosis

The nature and origin of two de novo small marker chromosomes found at prenatal diagnosis were determined by fluorescence in situ hybridization using chromosome centromere-specific probes and chromosome-specific plasmid libraries. One marker was found in a mosaic state and was shown to be an i(18p). The second marker was characterized as an inv dup(22). We conclude that molecular cytogenetic analysis contributes to the identification of marker chromosomes and therefore facilitates genetic counselling and decision-making for the parents.