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61.
CharacteristicsofphosphoruschemistryanditsgeographicaldistributionintheHaiheRivervalley,NorthChinaJiangGaoming;HuangYinxiao;L...  相似文献   
62.
YellowRiverValleyfloodanddroughtdisaster:spatial-temporaldistributionpredictionandearly-warningGaoLin,ShaWanying,LiuHuaiquan,...  相似文献   
63.
处理含油废水絮凝剂最佳配方的筛选   总被引:1,自引:0,他引:1  
针对含油废水,选择合适种类的絮凝剂,通过评价絮凝剂的除油效果,筛选出适合处理石油化工行业含油废水的絮凝剂最佳配方.其主要特点是投加量少、除油效果好、价格适宜。  相似文献   
64.
汞污染河流底质迁移模式研究   总被引:5,自引:1,他引:5       下载免费PDF全文
对蓟运河下游汞污染底质迁移过程的研究表明:在水流作用下,底质的重新悬移在其过程中起主要作用.在过去七年中,由这一作用带入渤海的汞为16.6t.本文提出了一种数学模式来描述这一过程.与实测数据对比,模式计算结果具有较好的精度(误差为16.4%)和重现性.用模式预测出底质中汞浓度降至目前二分之一所需时间为9—10年.  相似文献   
65.
An advanced cost-saving method of removal of high-As(Ⅲ) from SO4(-Ⅱ)-rich metallurgi cal wastewater has been developed by diluting the SO4(-Ⅱ) content with As(Ⅲ)-Cl(-Ⅰ)-rich metallurgical wastewater and then by the direct precipitation of As(Ⅲ) with Fe(Ⅲ) at pH2.3.As(Ⅲ) removal at various SO4(-Ⅱ)/Cl(-Ⅰ) molar ratios and temperatures was investigated The results showed that 65.2–98.2%of As(III) immobilization into solids occurred at the SO4(Ⅱ)/Cl(-Ⅰ) mo...  相似文献   
66.
Congenital nephrosis is an autosomal recessive disorder requiring neonatal renal transplant for survival. The postnatal diagnosis rests upon the electron microscopic evaluation of the epithelial foot processes and basal membrane of the glomeruli. The prenatal diagnosis can be suspected in the presence of a positive family history with an amniotic fluid (AF) alpha-fetoprotein level greater than 5 standard deviations (SD) above the population mean accompanied by a negative AF acetylcholinesterase, absent haemoglobin F, and an unremarkable fetal sonographic examination. We reviewed our series of seven cases of congenital nephrosis fulfilling the above criteria; four cases had negative family histories, and in two cases the diagnosis of congenital nephrosis was further supported by the presence of elevated AF albumin concentrations. We conclude that (1) the prenatal diagnosis of congenital nephrosis is feasible in a low-risk population, and (2) an elevated AF albumin concentration may represent an additional marker for the diagnosis of congenital nephrosis, even though false-negative results have been reported.  相似文献   
67.
Microbial flocculant and its application in environmental protection   总被引:11,自引:2,他引:11  
1IntroductionAlotofvariedflocculantshavebeenusedinwastewatertreatment,dredgingdownstreamprocessingandsomeindustrialfieldincl...  相似文献   
68.
One hundred and fifty-one women of advanced maternal age who underwent genetic termination of pregnancy (TOP) were studied for their reproductive behaviour and the type of procedure for prenatal diagnosis in a subsequent pregnancy. A total of 59 women (39 per cent) had a further pregnancy. In all continuing pregnancies prenatal diagnosis was performed, of which 75 per cent consisted of chorionic villus sampling (CVS). Reproductive behaviour following a genetic termination was negatively correlated with maternal age and parity. Both reproductive behaviour and the choice to undergo a diagnostic procedure in the next pregnancy were independent of the type of diagnostic procedure in the previous affected pregnancy.  相似文献   
69.
The sinusoidal fetal heart rate pattern has been described in association with severe fetal anaemia, with fetal hypoxaemia, and with the administration of parenteral narcotics. Here, we report a case of decreased fetal movement in which a sinusoidal tracing was recorded. The sonographic diagnosis of a massive fetal intracranial haemorrhage was made. A non-interventive approach was taken and the fetus died soon after in utero. We review 28 previous cases in which the prenatal sonographic diagnosis of fetal intracranial haemorrhage was made, including the underlying maternal and fetal factors and neonatal outcomes. We propose that the sinusoidal tracing in this case was due to the intracranial bleed and suggest that fetal intracranial haemorrhage be considered in the sonographic evaluation of the fetus with a sinusoidal pattern.  相似文献   
70.
A prenatally detected case of a rare mosaic tetrasomy 12p/trisomy 12p is reported, presenting as the well-known accessory isochromosome 12p and a supernumerary single 12p marker in 17/24 and 6/24 clones of cultured amniotic fluid cells, respectively. The chromosomal nature of both marker chromosomes was investigated in cultured amniotic fluid cells by fluorescent in situ hybridization with various probes: the 12-centromeric probes pa12H8 and D12Z3, a whole chromosome 12 paint, and the chromosome 12p-specific paint M28. DNA analysis revealed a maternal origin of the extra 12p material. After counselling, the parents requested termination of pregnancy. Inspection and autopsy of the fetus revealed many of the dysmorphisms and internal structural abnormalities of the Pallister–Killian syndrome.  相似文献   
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