蓄能器爆炸事故原因推断及防控措施

囊式蓄能器是液压系统中常用的压力容器。在更换胶囊和(或)充装氮气时如操作不当,有发生爆炸的风险。通过对一起蓄能器爆炸事故的调查,经计算、推论,得出此次爆炸是一起物理爆炸。并就事故发生原因及其爆炸强度、危害程度进行了分析。提出生产商和使用单位应制定科学的、可行的标准操作程序(Standard Operation Program,SOP),并要求工人在实际操做中严格执行,加强过程控制,避免事故的发生。     

Abnormal immunological development in fetuses with trisomy 18

Flow cytometry was used to enumerate the lymphocyte subpopulations in fetal blood obtained by cordocentesis from eight trisomy 18 fetuses at 20–36 weeks' gestation. Compared with values in chromosomally normal fetuses, in trisomy 18 the mean T- and natural killer (NK) cell counts were significantly lower (t= − 7·63, P<0·001 and t= − 3·58, P<0·01, respectively); the mean B-cell count was not significantly different (t= − 1·32). These findings demonstrate that in trisomy 18 there is abnormal intrauterine development of the immune system.     

二种除草剂遗传毒性的研究

以黄鳝为试验材料,研究了艾割和使它隆二种除草剂对鱼类的致突变性。对经腹腔注射染毒上述二种除草剂的受试黄鳝,通过对其活体肾细胞染色体数目和形态的观察,分析其突变率。研究结果(经t检验)显示:艾割和使它隆二种除草剂分别在其试验最低受试剂量50mg/kg和8.0mg/kg即可引起黄鳝的染色体畸变。采用SOS/Umu显色试验研究,在SOS/Umu试验中,使它隆和艾割2个受试除草剂可以诱发SOS阳性反应,且呈明显的剂量-效应关系。试验表明这二种除草剂具有遗传毒性,应对这二种除草剂严加管控,避免其对环境的影响。     

Prenatal diagnosis of a de novo complex chromosomal rearrangement involving four chromosomes

A complex chromosome rearrangement, apparently a balanced translocation involving chromosomes 4,6, 15 and 16, was found in cultured cells of amniotic fluid from a 32–year-old primigravida who requested amniocentesis for prenatal diagnosis because of a family history of mental retardation. Chromosome analysis of peripheral blood from both parents were normal. The couple was counselled for the prenatal diagnosis of this de novo complex translocation and, subsequently, elected to terminate the pregnancy. Post-mortem examination revealed a 23–week fetus with intrauterine growth retardation. The identical chromosome rearrangement was subsequently confirmed in cultured fibroblasts from skin and cord obtained from the abortus. To our knowledge, this is the first report where routine prenatal diagnosis revealed a fetus with a balanced complex chromosomal rearrangement involving four chromosomes of de novo origin.     

Women's choices for fetal chromosome analysis

Five hundred and eighty women aged 35 or more at the expected date of delivery were offered the chance to join the MRC trial comparing CVS and amniocentesis at Queen Charlotte's Hospital. After a 1 h non-directive counselling session, they were asked to choose between having no test, having amniocentesis, or joining the trial in the hopes of having CVS (or in some cases having CVS outside the trial). The majority of women chose to have some test, and CVS was a more popular choice than amniocentesis.     

Cross-hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common chromosomal aneuploidies by fish

In a routine application of commercially available centromeric DNA probes for the prenatal screening of common trisomies involving the autosomes 13, 18, and 21, and sex chromosomes, four cases of discrepancy between fluorescence in situ hybridization (FISH) results and follow-up cytogenetic analysis were observed from a total of 516 cases of amniocentesis. In three of these cases, the results were false negative, and in one false positive. In this case, amniocentesis was performed because of a positive triple test in a 34-year-old woman with previous infertility treatment. The alpha satellite DNA probe for chromosomes 13/21 revealed five signals in 50 per cent of uncultured amniocytes, while standard cytogenetic analysis showed a normal karyotype. FISH analysis on metaphase chromosomes demonstrated the location of the additional signal in the centromeric region of chromosome 22. This additional signal was also present in the centromeric region of chromosome 22 of the mother, providing evidence for a possible inherited polymorphism in chromosome 22 responsible for unspecific hybridization with the alpha satellite probe for chromosomes 13/21 in this case. The observed polymorphism in centromeric regions may contribute to unreliability of the use of the 13/21 alpha satellite probe for prenatal screening by FISH.     

Chromosomal prenatal diagnosis: Study of 936 cases of intrauterine abnormalities after ultrasound assessment

Nine hundred and thirty-six prenatal chromosomal analyses were performed by four cytogenetic centres after ultrasound diagnosis of fetal abnormalities, amniotic fluid disorders, fetal growth retardation, and fetal or placental abnormalities. During the same period, 6515 fetal karyotypes were analysed because of maternal age. Frequencies of chromosomal aberrations in each case were respectively 4·4, 6·7 and 15·8 per cent, compared with 3·18 per cent when the fetal karyotype was performed because of maternal age. High rates of chromosomal aberrations are observed in cases of cervical hygroma, limb abnormalities, omphaloceles, duodenal stenosis, hydrocephalus, and facial abnormalities. In the case of polymalformations, this rate was 29·2 per cent. When malformations were seen together with an amniotic fluid disorder or growth retardation, 21·5 per cent chromosomal aberrations were observed. This frequency was 10·4 per cent when growth retardation was associated with an amniotic fluid disorder. Trisomy 13, 18, 21 and monosomy X accounted for 4/5 of all abnormalities in which we observed a high rate of triploidies (4·9 per cent) and balanced (3·3 per cent) or unbalanced (9·8 per cent) non-Robertsonian structural abnormalities. Sonographic ascertainment of these aberrations and prenatal characteristics of major anomalies are discussed.     

染色体步行PCR技术

染色体步行是一种常用的克隆已知基因旁侧序列的技术.本文综述了现有的染色体步行PCR技术,如反向PCR、锅柄PCR、连接介导PCR、热不对称PCR、SON PCR等,并在此基础上提出了一种新的染色体步行PCR技术的构思.它运用特异引物与随机引物的搭配,在普通PCR程序下扩增目的序列.实验中设置相应随机引物的RAPD对照,识别非目的扩增产物.文中介绍了新方法的原理,分析了这种方法的优缺点.这种方法可能是一种新的有效进行染色体步行的PCR技术,国内外尚未见相关报道.图2参26     

金钟藤的年轮生长量与气候因子的相互关系

分析了金钟藤(Merremiaboisiana(Gagn.)vanOoststr.)的年轮特征,并探讨了它与温度等气候因子的关系。金钟藤的年轮极不规则,有许多自然隆起和裂缝。金钟藤的年轮生长量通过格子法来估算。结果表明金钟藤年轮的年平均生长量与温度呈极显著正相关,与降水、日照时数和相对湿度相关性不显著。罗浮山地区降水和日照时数基本能够满足金钟藤的生长,结合相关研究结果推测:温度可能是金钟藤快速生长的主要驱动因子。     

电离辐射对人类染色体的影响

通过对２６例静电加速器工作者染色体的观测，研究电离辐射引起的人类染色体畸变。效应与辐射剂量相关，畸变的类型和频率反映细胞损伤程度。