Electrical detection of nuclear spin echoes

We show, via a straightforward calculation, that it is feasible to detect nuclear spin echoes in a ferromagnetic thin film by electrical means. The detection scheme is based on the deflection of the electronic magnetization when the nuclear magnetization reforms during an echo. This deflection is observed as a time-dependent magnetoresistive signal.     

纵横扩张的优化

得到了最小折数纵横扩张的判别准则．针对4-正则图的平面嵌入的纵横扩张的特殊性，给出了它的最小折数纵横扩张判别准则．     

极紫外望远镜各通道夹角的测量

极紫外望远镜是由四个单通道的望远镜捆绑在一起,以便同时对太阳的相同部分观测,由于受地面装调以及发射过程中的影响,无法保证四个通道光轴严格平行,必然带来观测位置上的误差。只要测出各通道之间的光轴夹角,便可在像面上采取适当的处理方法,以便减小这种误差,但这一夹角的测量精度必须控制在0.1″内。为达到如此高的精度,采用了太阳局部边缘探测的方法,很好地解决了这一问题。     

一种改进的数字散斑相关方法用于检测人的口型变化

提出了一种基于数字散斑相关测量技术的口型变化检测技术,该技术以白光数字散斑相关测量方法为基础,根据实际应用的需要,引入重心算法并进行了改进,可以实时地检测人说话时的口型变化。通过实验表明,提出的方法是一种实用的、快速、高精度的口型变化测试方法,可为今后的唇语识别技术奠定基础。     

免疫珠技术快速检测腹泻性大肠杆菌

采用表面光滑玻璃珠作为载体材料，用1：40的腹泻性大肠杆菌诊断血清进行包被。可制成免疫珠。这种免疫珠能与腹泻性大肠杆菌发生特异性结合。经乳糖蛋白胨培养液培养，然后根据其产酸产气进行判断。能在18h内完成腹泻性大肠杆菌的检测。其灵敏度为样液中含有腹泻性大肠杆菌数必须大于10CFu／mL．该法简单、快速、易操作、灵敏度高。     

Memory effects in gas chromatographic detection with a microwave-induced plasma

Capillary gas chromatography coupled to microwave-inducedplasma detection furnishes sensitivity adequate for trace analysis when the signal is monitored at a carbon emission line. Work performed with one of these systems at high electronic gain for the carbon signal has revealed solvent band widths in excess of four minutes; these impeded quantification of peaks eluting after the solvent. This report discusses two phenomena which could be related to the unexpected intensity of this solvent response: photomultiplier tube saturation and carbon deposits in the quartz plasma discharge tube.     

Energy transfer between the flavin chromophores of electron-transferring flavoprotein fromMegasphaera elsdenii as inferred from time-resolved red-edge and blue-edge fluorescence spectroscopy

Both a mode-locked argon-ion laser and synchrotron radiation were used as excitation sources to obtain time-resolved polarized fluorescence of the two FAD cofactors in electron transferring flavoprotein fromMegasphaera elsdenii. Red-edge excited and blue-edge detected fluorescence anisotropy decay curves did not contain a fast relaxation process which was observed upon mainband excitation and detection. This relaxation was assigned to homo-energy transfer between the two FAD cofactors. Failure of energy transfer as observed with edge spectroscopy on this protein excludes restricted reorientational motion of the flavins as a possible mechanism of depolarization. From the global analysis of the fluorescence anisotropy decay surface obtained at multiple excitation and detection wavelengths, the distance between and the relative orientation of the flavins could be estimated. The methodology described has general applicability in other multichromophoric biopolymers and has the potential to acquire accurate geometrical parameters in these systems.     

单循环赛赛程安排的一个图论方法

利用图论的边着色理论建立了一个赛程安排的数学模型 .首先建立 n支球队与完全图 Kn的 n个顶点间的一一对应 ,把球队 Ai和 Aj间的比赛关系抽象成 Kn的顶点 i和 j间的边 ( i,j) .然后分别构造出了图K2 m- 1和 K2 m的正常 2 m-1边着色 .从而给出了各球队每两场比赛间得到的休整时间最均等 ,休整的间隔场次数达到上限值 n2 的一个赛程安排方案     

High-Throughput Screening of Ten Microcystins and Nodularins, Cyanobacterial Peptide Hepatotoxins, by Reversed-Phase Liquid Chromatography-Electrospray Ionisation Mass Spectrometry

Liquid chromatography-electrospray ionisation mass spectrometry was evaluated in the high-throughput analysis of microcystins and nodularins, cyanobacterial peptide hepatotoxins. Extracts originating from cyanobacterial strains and field material were separated on a 30 mm × 4 mm I.D. Merck Purospher STAR RP-18e column using a rapid gradient of aqueous formic acid and acetonitrile, ionised by electrospray technique and analysed on a Micromass Quattro II triple-quadrupole mass spectrometer operated in the selected ion recording (SIR) mode. The total analysis time per sample was 2.8 min corresponding to 514 samples a day. The system showed good robustness during a series of 320 repetitive injections of a field sample containing three major microcystins.