森林植被影响径流形成机制研究进展

径流形成机制研究在水文学领域中具有十分重要的意义,且受到越来越广泛的重视。水文环境以及水文通量的空间异质性和时间变化性导致了水文过程的尺度依赖性和非线性特征,没有对水文过程较为清晰的认识,就不能将某一地区某一流域森林植被变化水文生态效应的研究结果简单地外推到其他地区和其他流域。开发基于物理过程分布式参数水文模型可以为认识森林植被变化的生态学后效和客观评价森林植被水文生态效益提供可行的工具。但是要实现这一目标,研究森林植被影响径流形成机制是问题的核心所在。另一方面,认识森林影响径流形成机制有助于研究水文学中的尺度问题。研究森林植被影响径流形成机制的主要方法包括水文测验、同位素示踪和动力水文学计算等,研究的空间尺度则为坡面与流域相接合。从已有的研究成果来看,森林植被影响径流形成机制可以概括为:①森林流域径流形成为变动源区产流机制;②森林流域径流形成主要受饱和地表径流、亚表层径流和地下径流的控制;③森林流域径流形成机制是相互作用和相互转化的;④优先流在森林流域径流形成中起到了至关重要的作用。     

镀液循环流量对封闭循环电沉积Ni-SiC复合镀层的影响

目的 研究封闭式镀液循环装置中不同镀液循环流量对Ni-SiC复合镀层的影响规律,优化镀液循环流量参数.方法 以Q235管状工件为待镀基体,以添加SiC颗粒的改良瓦特镀液为母液,在自主研发的封闭式镀液循环电镀装置中以0.3、0.5、0.7 m3/h的镀液循环流量于管件内壁制备Ni-SiC复合镀层,通过SEM检测、XRD测试、硬度测试和摩擦磨损性能测试等手段,对各Ni-SiC复合镀层宏微观形貌、厚度、成分、结构、硬度和耐磨性进行分析研究.结果 在0.5 m3/h流量条件下,镀层厚度为32.98μm,SiC颗粒含量为15.37％,镀层晶粒尺寸和硬度分别为10.84 nm和704HK0.245,该条件下制备的Ni-SiC复合镀层具有最佳耐磨性,摩擦系数为0.41,体积磨损率仅2.83×10–5 mm3/Nm.结论 在不同镀液循环流量参数下,采用该封闭式循环电镀装置,均可制得均匀完整的Ni-SiC复合镀层.随镀液循环流量的升高,镀层厚度和SiC颗粒体积含量均降低,镀层颜色金属光泽增强,镀层晶粒尺寸先减小、后增大,镀层硬度则先升高、后降低.     

Association of generalized dystrophic epidermolysis bullosa with positive acetylcholinesterase and markedly elevated maternal serum and amniotic fluid alpha-fetoprotein

A case of fatal generalized dystrophic epidermolysis bullosa is described in a prematurely born female whose mother had strikingly elevated mid-trimester serum and amniotic fluid alpha-fetoprotein concentrations, a positive amniotic fluid acetylcholinesterase band, and negative serial ultrasound studies. This case lends further support to an association between autosomal recessive generalized dystrophic epidermolysis bullosa and increased levels of alpha-fetoprotein, positive amniotic fluid acetylcholines'terase, and normal ultrasound findings.     

Pallister-Killian syndrome diagnosed by chorionic villus sampling

The first prenatal diagnosis of Pallister-Killian syndrome by chorionic villus sampling is presented. Fetal hydrops was noted on ultrasound in early pregnancy, and the karyotype revealed isochromosome 12p mosaicism.     

Cystic hygroma: Prenatal diagnosis and genetic counselling

Six cases of cystic hygromas detected during second trimester ultrasound examination are reported: 4 fetuses (67 per cent) had a 45, X karyotype, 1 fetus had trisomy 18, 1 fetus had a normal karyotype (46,XX) and at autopsy multiple anomalies were observed. In the latter case the family history suggested an autosomal recessive pattern of inheritance. In order to reach a definite diagnosis and give proper genetic counselling when a fetus is found to have cystic hygroma, a fetal karyotype as well as a family and reproductive history should be obtained.     

Effects of mid-trimester induced abortion on the subsequent pregnancy

The outcome of the pregnancy following (a) a mid-trimester termination of pregnancy (TOP) for fetal neural tube defect (NTD) (77 women=group 1); (b) mid-trimester TOP for fetal Down's syndrome (13 women=group 2); (c) delivery of a baby with NTD (119 women=group 3) was studied. The prenatal fetal loss was relatively high in all groups. In group 1 it was similar to that found in other studies after first trimester TOP, in group 2 it was associated with advanced maternal age and the unexpected finding in group 3 was not attributable to advanced maternal age. It is suggested that a previous NTD per se might increase the risk of fetal loss in the next pregnancy. A previous mid-trimester TOP for NTD was not associated with an increase in premature labour, small for dates babies or congenital abnormality in the next pregnancy, but there was a slight increase in the number of babies weighing less than 2500 g.     

The safety of fetoscopy: (I). Effect of umbilical vessel puncture on the fetal heart rate and cord histology

The fetal heart rate (FHR) was continuously monitored during 42 umbilical vessel punctures performed at the placental insertion of the cord in 24 diagnostic fetoscopies in which pure fetal blood was obtained. In only one patient did a deceleration first appear during puncture and aspiration of fetal blood. In two patients decelerations preceded fetoscopy and in two others they began during the fetoscopy but before puncture of an umbilical vessel. In 19 patients, the FHR did not change at all during the procedure. Fetal haemorrhage after sampling was either absent or minimal. Six pregnancies were terminated because a positive diagnosis had been made and 18 healthy babies were born. Umbilical cords were examined after 7 terminations of pregnancy and after 6 deliveries. In the former group the puncture could just be seen with the naked eye and the needle track was demonstrated histologically in 6. No traces of the puncture or other abnormalities were found in the cords after delivery. Fetal blood sampling from umbilical cord vessels, particularly at the placental insertion of the cord, is the technique of choice since pure fetal blood can be obtained without increasing the risk of fetoscopy.     

降低气流粉碎过程中噪声强度的研究

主要报导了超音速气流超细粉碎过程中噪声产生的原因、影响因素及降低噪声强度所采取的技术原理途径与措施。研究结果表明 :采用CSQ消声装置完全可以将超音速气流粉碎过程中产生的噪声 130dB(A)降低到国家规定的标准 85dB(A)之下。该装置结构简单 ,既能消除噪声 ,又便于产品卸料 ,拆卸清理方便 ,综合性能良好。     

旋进型颗粒层除尘器的研究与试验

本文阐述了一种新型二级立式族进型颗粒层除尘器，它的关键技术采用独创的床外清灰及气流输送、滤料循环系统。该除尘器适用范围广、除尘效率高、成为新一代的除尘器专利产品。     

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.