LY12CZ铝合金在EXCO溶液中的腐蚀行为研究

研究了35℃条件下LY12CZ铝合金在质量分数为20％的EXCO溶液中的腐蚀行为。利用体视显微镜测量了试样的最大腐蚀深度。实验中发现平行试样之间的最大腐蚀深度具有分散性．经检验确定其分布规律符合正态分布。实验数据表明LY12CZ铝合金在质量分数为20％的EXCO溶液中的腐蚀过程可分为3个阶段：最初的14h内符合S型曲线规律．为点蚀的萌生及发展阶段：随后发展为剥蚀阶段．其中14～120h呈线性规律,120h后呈二项式规律发展至实验结束。     

LY12CZ铝合金腐蚀损伤的概率分布及其变化规律

采用铜加速乙酸盐雾试验方法对LY12CZ铝合金腐蚀行为进行了研究。结果表明：腐蚀深度服从Gumbel分布、正态分布、威布尔分布和对数正态4种分布。选用正态分布描述了LY12CZ铝合金在盐雾环境下的腐蚀损伤的分布特性,并得出了不同置信度和可靠度下腐蚀深度随时间变化的规律。     

基于STC12C5410AD的电铃无线控制系统

针对传统电铃采用单一作息时间表进行专线控制的缺点,设计了一种能无线控制、又能同时存储多个作息时间表的电铃控制系统．该系统用无线代替专线,存储有多个时间表,在季节变更时通过控制器自动变换表,解决了传统电铃控制系统中的专线成本高、维修难、季节变换需要人工改表的问题．图5,表2,参4．     

20世纪重大自然灾害评析

人类在科学技术上取得了辉煌成绩的同时,在认识自然和改造自然方面也得到了才识和新的认识,这一教训主要是来自自然灾害。根据收集到的全球自然灾害有关数据,对２０世纪全球主要自然灾害特征分布特点进行了分析,并对其成因提出了看法。     

用12SrRNA基因序列研究潮龟科（BATAGURIDAE）闭壳龟类的进化

测定了潮龟科（Ｂａｔａｇｕｒｉｄａｅ）具闭壳结构的齿缘摄龟属（Ｃｙｃｌｅｍｙｓ）、锯缘摄龟属（Ｐｙｘｉｄｅａ）、闭壳龟属（Ｃｕｏｒａ）共６种线粒体１２ＳｒＲＮＡ基因片段的序列,结合潮龟科其它一些属的序列数据,探讨了具闭壳结构龟类的起源与进化以及闭壳龟属的分类学问题．认为闭壳龟属与锯缘摄龟属为姐妹群,两者与齿缘摄龟属的亲缘关系较远,提示这些具闭壳结构的龟类可能不是由一个共同祖先分化而来．本文的结果不支持将闭壳龟属拆分为闭壳龟属和盒龟属两属     

可持续发展战略与上海“十五”计划编制的研究

“十五”计划是上海市进入21世纪的第1个5年计划,从提升自身发展质量和国际综合竞争能力的要求分析了将可持续发展战略纳入上海“十五”计划编制工作的必要性和重要性,围绕思想创新、目标创新、框架创新、指标创新等4个方面探讨了以可持续发展为定位的上海“十五”计划编制思路。     

铅诱导的PC12细胞凋亡及caspase-3的激活

用MTT法及TUNEL法检测醋酸铅对PC12细胞活力和凋亡率的影响,并用荧光标记的特异性caspase-3抑制剂来测量caspase-3的激活.结果显示,PC12细胞暴露于浓度为0.1、1、10、100 μmol·L-1的醋酸铅中24 h后,凋亡率和caspase-3的激活显著增加,并具有剂量-效应关系;当铅浓度达到1 μmol·L-1及以上时,细胞活力明显下降.因此可以推论,铅能够诱导PC12细胞发生凋亡,caspase-3的激活可能在这过程中起了非常重要的作用.     

Prenatal diagnosis of Pallister–Killian syndrome: Resolution of cytogenetic ambiguity by use of fluorescent in situ hybridization

We report a case of Pallister-Killian syndrome initially diagnosed prenatally as tetrasomy 21. A 33-year-old primiparous woman was noted at 24 weeks' gestation to have moderate polyhydramnios. Ultrasonography showed diminished fetal stomach filling, hydronephrosis, and prominence of the cisterna magna. Cytogenetic analysis of cultured amniocytes was initially interpreted as mosaic tetrasomy 21: 46,XX/47,XX,+i(21q). The patient was then referred to our centre for genetic counselling. At 34 weeks' gestation, a dysmorphic infant was delivered and died within 30 min. Physical features were consistent with the Pallister-Killian syndrome. Renal, gastrointestinal, and central nervous system anomalies were found at post-mortem examination. Analysis of peripheral lymphocytes revealed 5 per cent of cells with a marker chromosome, while 92 per cent of cultured fibroblasts had this same marker. Fluorescent in situ hybridization (FISH) using an alpha-satellite probe for chromosomes 13 and 21 failed to hybridize to the marker, while a chromosome 12 centromeric probe unequivocally identified it as an i(12p). Use of FISH can provide rapid, specific prenatal diagnosis of ambiguous marker chromosomes and improve prenatal counselling.     

红球藻水生748株(Haematococcus sp.HB748)培养基的选择与对维生素B_(12)的需求

比较了红球藻HB748株在MCM，BBM及BG－11．3种培养基中的生长．结果表明：HB748在这3种培养基中前4d的平均生长速率分别为0．97d－1，0．77d－1和0．63d－1，存在显著差异；然而，在BBM和BG－11中添加MCM中所含等量VB12后，748株在3种培养基中的生长速率趋于一致，表明VB12，是HB748维持较好的前期生长的必需成分；在VB12的需求满足后．3种培养基无机组分的差异对HB748前期生长影响甚微．     

Prenatal diagnosis of tetrasomy 12p by in situ hybridization: Varying levels of mosaicism in different fetal tissues

Prenatal diagnosis of tetrasomy 12p is complicated by the discrimination of the 12p isochromosome from the duplication 21q as well as the level of mosaicism demonstrated in the particular tissue sampled. In this disease, a high percentage of chromosomally abnormal cells are generally found in fibroblastic cells, but lymphocyte karyotypes from the same individual may be normal. We report on the pregnancy of a 37-year-old female who presented to our centre at 16 weeks' gestation for genetic amniocentesis. Sonography of the fetus revealed dextrocardia and diaphragmatic hernia. Chromosome analysis of amniocytes demonstrated mosaicism of a 47,XY,+i(12p) line in 80 per cent of cells and a normal male line (20 per cent), consistent with the Pallister-Killian syndrome. Following termination, a 220 g male fetus of 18 weeks was examined. A flattened nose and low-set ears were noted. In situ hybridization with a chromosome 12 centromeric probe in lymphocytes and skin cells unequivocally confirmed the karyotype and showed the presence of a single centromere in the abnormal chromosome, suggesting a true isochromosome. Chromosome analysis of various fetal tissues was performed and the following percentages of abnormal cells were found: skin 100 per cent, chorion 50 per cent, placenta 30 per cent, and blood 80 per cent. The high frequency of tetrasomic cells in fetal blood at this early gestational age is noteworthy, since most reports of this syndrome show a very low percentage of abnormal cells postnatally.