地下感应式通信理论的研究

本文研究了地下矿井内,电波沿巷道内线缆传播的可行性及单线波模的传播与衰减规律,研究巷道内电小天线与线缆之间的耦合情况,从而为实际工作提供理论依据。     

英汉交际语差异及其原因初探

文章就日常生活中一些较为典型的交际情景，对英汉交际语的差异及其潜在原因作了探讨。     

A latent class probit model for analyzing pick any/N data

A latent class probit model is developed in which it is assumed that the binary data of a particular subject follow a finite mixture of multivariate Bermoulli distributions. An EM algorithm for fitting the model is described and a Monte Carlo procedure for testing the number of latent classes that is required for adequately describing the data is discussed. In the final section, an application of the latent class probit model to some intended purchase data for residential telecommunication devices is reported. Geert De Soete is supported as “Bevoegdverklaard Navorser” of the Belgian “Nationaal Fonds voor Wetenschappelijk Onderzoek.”     

植物药超氧物歧化酶活性与某些性质的研究

应用NBT光还原法对23种植物药材SOD粗提液活性研究表明。供试材料全部达到200units·g~(-1)F·W的水平,13种超过300units·g~(-1)F·W,野山楂高达812.5units。酶的比活,玄参、何首乌位列前茅,超过300units·mg~(-1)protein~-,野山楂、枸杞等都在150units·mg~(-1)protein~(-1)以上。综合分析,何首乌、野山楂、玄参与枸杞等酶活性与比活都高,有开发利用的价值。植物药普遍具有Mn-SOD与Cu·Zn-SOD,本研究首先发现枸杞、宁夏枸杞、沙参和合子草具有Fe-SOD。酶粗提液的热稳定性明显优于纯化酶。     

MeV Pb离子在非晶Si中的射程离散──离子束混合和增强扩散的影响

１．０ＭｅＶ２０８Ｐｂ离子在非晶Ｓｉ中的投影射程ＲＰ和射程偏差ΔＲＰ作为注量和温度二者的函数用背散射法进行测定．注量的变化范围为５×１０１３～７×１０１４ｃｍ－２．注入是在室温和ｔ＝－１２０℃下完成的．由由实验所确定的投影射程，射程偏差与注量或温度无关，并且分别等于２９５和７２．２ｎｍ．与ＴＲＩＭ８６的计算结果相比较，发现ＲＰ的偏离为１８％，而ΔＲＰ的偏离为３６％．ＲＰ和ΔＲＰ二者与注量及温度的无关性，排除了所观察到的与ＴＲＩＭ的矛盾是由于注入期间辐射增强扩散或离子束混合效应而引起的解释。     

氧化物半导瓷中晶界势垒的起源

提出了一个关于氧化物半导瓷晶界势垒起源的新观点，认为晶界势垒起源于烧结过程中外界氧在晶界中的扩散，与材料的结构、化学缺陷、掺杂、外界气氛、烧结工艺、组成状态等有密切关系，并用此理论解释了许多实验现象。     

域外奇点法分析薄板的平面应力问题

本文推导了两边简支无限长薄板平面应力问题的基本解，该基本解为级数解，为了便于应用和提高计算精度，还求出了这些级数的和函数。把该基本解应用在域外奇点法中可分析一对边简支另一对边为任意的矩形薄板的平面应力问题。本文给出的算例表明该法有计算量少、精度高的优点。     

交织扩展Golay码编译码器实现方案的研究

论述了交织编码的工作原理，给出了一种交织扩展Ｇｏｌａｙ码的改进型软件设计方案，用ＴＭＳ３２０Ｃ２５实现了其编译码器并给出了模拟实验结果。实验结果表明，它能准确地纠正不大于７２比特位的差错；处理１２８×１２８×８比特位的一幅图像数据的运行时间为０．４１２ｓ．     

Aspirin-like drugs may block pain independently of prostaglandin synthesis inhibition

Summary Using flurbiprofen, a chiral anti-inflammatory and analgesic 2-arylpropionic acid derivative, the enantiomers of which are not converted to each other (less than 5%) in rats or man, we obtained evidence that prostaglandin synthesis inhibition is primarily mediating the anti-inflammatory activity but prostaglandin synthesis independent mechanisms contribute to the analgesic effects. Thus, the S-form inhibited prostaglandin synthesis, inflammation and nociception in rats. The R-form had much less effect on prostaglandin synthesis and did not affect inflammation. It did, however, block nociception in rats almost as potently as the S-form. S-flurbiprofen, in contrast to the R-form, was clearly ulcerogenic in the gastrointestinal mucosa. These results indicate additional molecular mechanisms of analgesia and suggest the use of R-arylpropionic acids as analgesics.