The characteristic of in situ stress in outburst area of China

In order to obtain the characteristics of in situ stress field in outburst mining area, using the hollow inclusion (HI) technique to measure the in situ stress of coal and gas outburst mining area. The measurement sites located in northeast, middle and east of china, which include eight mining areas such as Fuxin, Pingdingshan, Hebi and Huainan. Base on the analysis of measurement data from outburst mining area, conclusions could be obtained as follow: (a) major principal stress and minor principal stress is horizontal stress and interim principal stress is vertical stress, and the type of outburst area’s stress field is dynamic stress field; (b) the major principal stress and minor principal stress are higher than other regions and the tectonic stress is outstanding; and (c) the ratio of major principal and vertical stress is decrease with the increase of depth and the type of stress field is likely transfer dynamic to static. Thus, in situ stress plays a key role during the occurring and development of coal and gas outburst, which is an important reason of severe outburst in China.     

护听器个人防护值验证技术

本文介绍了关于护听器实际防护值的研究数据,和用于护听器个人防护效果验证的方法,以及3ME-A-RfitTM听力防护验证系统。研究表明,护听器的标称降噪值对其实际防护值的指示性非常差,目前也还没有一个可靠的方法来使用护听器的标称值。3ME-A-RfitTM听力防护验证系统是使用实地真耳内置麦克风(F-MIRE)方法,在实际工作现场中快速、定量地测定护听器在具体使用者身上取得的个人声衰减值(PAR),让安全管理人员对员工实际获得的防护水平有清晰的了解。     

农牧交错区土地荒漠化与生物多样性研究--以宁夏盐池县为例

采用α-多样性指数即Shannon-Wiener指数、Simpson指数、群落均匀度指数Jsw和Js和β-多样性指数(相似性系数Cs)研究宁夏盐池县草原群落在不同荒漠化治理措施下(人工封育、退耕还林、撂荒)生物多样性变化.2002和2003年固定样地观测数据表明,到2003年,各样地的α-多样性指数均有不同程度的提高,以撂荒地和退耕还林地α-多样性变化较大.Simpson指数、Js指数变化最为明显,分别平均增加了140%、109%,Shannon-Wiener指数、Jsw指数次之,分别增加67%、49%.人工封育不同处理区α-多样性指数也有较大变化,由核心＞边缘＞外围,变为边缘＞核心＞外围排列次序.β-多样性的研究结果同样表明,各样地的种类组成发生了一定的变化.文章还进一步分析了引起生物多样性变化的主要原因.     

油松毛虫感染白僵菌后体内蛋白质、酯酶和多酚氧化酶的变化

采用分光光度法测定了油松毛虫(Dendrolimus tabulaeformisTsai et Liu)3~5龄幼虫被病原物白僵菌(Beau-veria bassiana)感染后,其体内蛋白质的含量和多酚氧化酶活性的变化;结果表明,被白僵菌感染后1~8d,虫体内蛋白质含量持续下降,而未感染的则变化不大;多酚氧化酶(PPO)的活性呈现出先升高后下降的趋势.利用聚丙烯酰胺凝胶电泳技术,分析了染菌后1~7d幼虫体内酯酶同工酶的变化;结果显示,染菌后的3、4龄幼虫体内酯酶同工酶酶谱与对照相比,酶带数量变化较大,未染菌的为3条酶带,感染病菌后变为1条和2条.与其相比,5龄幼虫染菌后酯酶同工酶的酶带数量没有变化,只是酯酶的活性及含量比对照有明显减弱趋势.图2表5参16     

Mosaicism for trisomy 12: Four cases with varying outcomes

Trisomy 12 observed in chorionic villus sampling (CVS) may reflect generalized mosaicism or indicate mosaicism confined to only the placenta. In this report, four cases of trisomy 12 observed in CVS or cultured placental biopsies with varying outcomes are presented. Seven dinucleotide repeat polymorphisms for chromosome 12 were used to determine the chromosome 12 origins in the fetus or child and to delineate the mechanism(s) that gave rise to the trisomy. In two cases (cases A and C), the mosaicism was confined to the placenta, resulting in normal liveborns. Although, in one case, the molecular results suggested an apparent duplication of one paternal chromosome 12 in the placenta, normal biparental inheritance was found in the diploid fetal cell line in both cases. In two other cases (cases B and D), trisomy 12 was observed in both extraembryonic and fetal tissues. In one of these pregnancies, a child was born by Caesarean section at 37 weeks because of intrauterine growth retardation and oligohydramnios, and resulted in neonatal death. Molecular markers and fluorescence in situ hybridization (FISH) revealed low-level trisomy 12 mosaicism in the spleen. In the fourth case, fetal abnormalities were detected on ultrasound and low-level trisomy 12 mosaicism was observed in amniotic fluid cells using conventional cytogenetics and FISH. Molecular markers revealed a maternal meiosis I non-disjunction of chromosome 12 in DNA from a cultured placental biopsy. Although predicting the outcomes of pregnancies involving confined placental mosaicism remains difficult, molecular techniques are valuable tools for distinguishing uniparental from biparental disomy and mechanisms of mosaicism.     

海洋原位化学探测核心技术的研究应用

化学传感器和化学分析器是海洋原位化学探测系统中的核心技术。本文从电化学、光纤化学和湿法化学分析等三个领域介绍了国际上化学传感器和化学分析器的研究和应用现状 ,比较了部分化学传感器和化学分析器的性能指标和优缺点 ,指出了海洋原位化学探测技术的发展趋势。与国外海洋原位化学探测技术的研究相比 ,我国在这方面的研究基本上还是空白 ,海洋原位化学探测技术已成为我国亟待发展的海洋高新技术之一。     

Evaluation of X,Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization

The major aneuploidies diagnosed prenatally involve the autosomes 13, 18, and 21, and sex chromosomes. Fluorescence in situ hybridization (FISH) allows rapid analysis of chromosome copy number in interphase cells. This prospective study evaluated the use of four commercially available centromeric DNA probes (DXZ1, DYZ1, D18Z1, and D13Z1/D21Z1) for direct analysis of uncultured amniocytes. One hundred and sixteen amniotic fluid samples were analysed by FISH and standard cytogenetics. This evaluation demonstrated that FISH with, X, Y, and 18 alpha satellite DNA probes could accurately and rapidly detect aneuploidies involving these chromosomes and could be used in any prenatal clinical laboratory. In contrast, the 13/21 alpha satellite DNA probe hybridizing both chromosomes 13 and 21 was unreliable for prenatal diagnosis in uncultured amniocytes.     

Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: A prospective study

A prospective study was undertaken to evaluate the use of fluorescence in situ hybridization (FISH) for the detection of trisomy 21 in interphase nuclei of uncultured amniotic fluid cells. Five hundred cases were analysed in situ and classified as normal or abnormal; the results were subsequently checked against the cytogenetic findings. Four hundred and ninety-three were correctly identified as normal with an 86·6 per cent average frequency of scored nuclei exhibiting two signals; six cases were correctly identified as trisomic for chromosome 21 with 81·7 per cent of scored nuclei exhibiting three signals; and one abnormal case involving an unbalanced chromosome 21·21 translocation was falsely scored as normal due to poor hybridization/detection efficiency. The method has been substantially improved and simplified so that it is suitable for the rapid detection of trisomy 21. As aneuploidy detection in interphase does not identify structural chromosome aberrations, it is not a substitute for fetal chromosome analysis.     

Molecular cytogenetic analysis of term placentae suspected of mosaicism using fluorescence in situ hybridization

In first-trimester chorionic villus sampling (CVS) for prenatal diagnosis, abnormal chromosomal findings, such as mosaicism, trisomies, or suspect abnormal karyotypes, are found more frequently than at amniocentesis. The fact that these chromosomal abnormalities do not always reflect the fetal karyotype but may be restricted to the placenta is a major problem in diagnosis and counselling. In this paper we present the results of fluorescence in situ hybridization (FISH) studies on interphase nuclei of three term placentae investigated because of false-positive findings at first-trimester CVS. The chorionic villi of the first case showed a mosaic chromosome pattern involving a trisomy 10 cell line and a normal cell line, those of the second case a total trisomy 8 cell line, while in the third case a complete monosomy X was found. Follow-up amniocentesis in each of these three cases revealed a normal karyotype. By using FISH, we were able to confirm the presence of the aberrant cell lines, which were all confined to one part of the placenta. FISH on interphase nuclei allows the investigation of large numbers of cells for the existence of numerical chromosome aberrations in a quick and reliable way.     

Rh-Al-MCM-41上NO选择性催化还原的原位红外研究

利用气-固相固定床反应装置考察了Rh交换的Al-MCM-41在高气体空速条件下对贫燃NOx的选择性催化还原活性,考察了氧含量对其的影响。结果表明,在200000h~(-1)的气体空速、O_2/C_3H_6=20、603K时,NO转化率为74.3％。利用原位FTIR技术研究了该催化剂的表面吸附物种及表面程序升温反应行为,并结合实验观察探讨了贫燃条件下Rh-Al-MCM-41催化剂上NO的选择性催化还原机理。