在实验上

This study examined the numbers and size distribution of stickies from three kinds of PSAs in pulping, post screening and post flotation stream. The results were used to determine the removability of the different stickies through screening and flotation.

参考该标准中的实验条件和检测方法，对不干胶纸所带的3种压敏胶在废纸回用过程中的去除特性，即循环适应性，进行了实验分析，比较了胶黏物在不同处理阶段的分散特点和去除差异，在此基础上，探讨了碎浆、筛选和浮选3个处理单元在胶黏物去除过程中的不同作用和关联影响，并结合 RCA 标准，对该胶黏剂的循环适应性作了分析评定。

A formula was proposed to explain the effects of secondary-scattering in the electron impact experiment, based on this formula, and the secondary-scattering coefficient as a function of the scattering angle was investigated.

在一定假设下利用公式解释了在电子碰撞实验中二次散射效应对实验测量的影响，并在此公式的基础上研究了对CO不同跃迁的二次散射系数随角度的变化关系。

The mutant △RSD-9 K141D was subcloned into the pGEX-6p-1 expression vector and the △RSD-9 protein was purified by GST affinity chromatography and digested by Prescission Protease to cut the GST domain. Next, to further verify the intracellular interaction of RSD-9/△RSD-9 and rtSH3p13 proteins, laser confocalization study and co-immunoprecipitation method were used.

随后，我们又运用蛋白质在细胞内的荧光共定位实验和免疫共沉淀实验，在细胞内相互作用水平上，证明了RSD-9蛋白/△RSD-9蛋白都与rtSH3p13蛋白在胞内相互作用。

MTT assay FAK signaling pathway inhibitor genistein on human corneal epithelial cell cytotoxicity;RT-PCR detection of human corneal epithelial cells adhesion to fungus at different times,extracellular matrix protein including laminin,fibronectin,FN glass,Ⅳcollagen,transmembrane protein integrinαⅤ,integrinβ1(ITGβ1),as well as the FAK signaling pathway FAK1,FAK2 and Paxillin gene expression;Western blot detection of the signal transduction pathway adhesion-associated protein ITGβ1,FAK and PAX expression and the inhibition of genistein. Immunocytochemical method was used to observe the LN,FN and FAK expression in human corneal epithelial cells during interaction with the fungues;Laser scanning confocal microscope had a cell positioning on FN,FAK and PAX,observed the changing of the human corneal epithelial cytoskeleton after stimulated by fungues;Quantitatived by flow cytometry to detect of human corneal epithelial cells with PAX at ITGβ1 fungal expression after adhesion;Optical microscopy quantitied the fungues and human corneal epithelial cell adhesion and recorded to determination the integral optical density afrer adhesion;Scanning and transmitted electron microscope observed the changing of cell ultrastructure after fungues and human corneal epithelial cell adhesion.

第一部分真菌激活人角膜上皮细胞FAK信号转导通路的体外实验研究将三种常见致病真菌(白色念珠菌、烟曲霉菌和茄病镰刀菌)分别与人角膜上皮细胞共孵育，MTT法检测FAK信号通路抑制剂染料木黄酮的对人角膜上皮细胞的细胞毒性作用；RT-PCR检测真菌黏附人角膜上皮细胞后不同时间细胞外基质层连蛋白、纤连蛋白、玻连蛋白、Ⅳ型胶原、跨膜蛋白整合素αV、整合素β1(ITGβ1)，以及FAK信号通路中FAK1、FAK2和桩蛋白基因的表达情况；Western blot的方法检测黏附信号转导途径相关蛋白ITGβ1、FAK和PAX的表达，以及染料木黄酮对真菌刺激人角膜上皮细胞FAK信息通路活化的抑制作用；免疫细胞化学方法观察人角膜上皮细胞与真菌相互作用过程中LN、FN和FAK的表达；激光共聚焦显微镜对FN、FAK和PAX进行了细胞定位，并观察真菌刺激后人角膜上皮细胞骨架的变化；流式细胞仪定量检测人角膜上皮细胞ITGβ1与PAX在真菌黏附后表达的改变；光学显微镜观察真菌与人角膜上皮细胞黏附数量，记录并测定了黏附后积分光密度值OD扫描及投射电镜观察了真菌与人角膜上皮细胞黏附后，细胞超微结构的改变。

The difference, relative variation of modular number and mass and their frequency distribution were analyzed between treatments, and within and among structural levels of genet, ramet and tiller in grazing experiment.

在放牧实验中，分别以矮嵩草源株、分株和分蘖层次为单位，对其构件单元的数量和生物量、变异系数、频率分布在处理间的差异和相对变异性进行分析；在模拟放牧实验中，分别就无性系内刈割和未刈割部分从这3个层次上比较了构件数量和生物量在处理间的差异和相对变异性，所得结果如下

this paper analyses the basic principle of tpc,compares the error performance in the system which has been applied with tpc with the uncoded system,studies the influences which different block codes and iterative numbers to tpc decode performance.under the circumstances of different iteration numbers and block codes,experiment simulation is carried on.the simulation results indicate that introduction of tpc can get the code gain of 5~6 db.tpc decoding algorithm is simple,and doesn′t have the error floor,the complexity of its hardware implementation is smaller,it is a kind of practical channel coding method.

摘 要：在分析turbo 乘积码的基本编译码原理的基础上，比较了未编码与编码后系统的差错性能，研究了选取不同分量码、不同迭代次数对tpc译码性能的影响。在不同迭代次数与分量码情况下，进行了仿真实验。仿真实验表明，在相同的差错性能条件下，采用tpc码能带来5~6 db的编码增益。tpc译码算法简单，没有错误平层，硬件实现复杂度较小，是一种非常实用的信道编码方式。

The experimental goal is to use SOPC-NIOSII EDA / SOPC system platform for real-time moving object detection system in this paper. After the inputs of image penetrated the CMOS Sensor to receive the data of the image makes the RGB form the transformation. The CPU processes operation of image detects. After the processed of image deliveres to VGA displayed output of real-time image. We use example programs of DE2 platfrom to achieve entire hardware on experiment board of SOPC-NIOSII EDA / SOPC System platform. On system of dectect image we divided into two parts : hardware and software. We use Verrilog of HDL to modify code in hardware. To use Custom IP of SOPC Builder produced IP of our need. We need a interface to connect in the COMS Sensor to FPGA and FPGA to VGA among. The code synthesize to create a programming file of *.S by Quartus II. Then, to use USB BLASTER of SOPC-NIOSII EDA/SOPC System platform programmed on FPGA. We use NIOS II IDE to assign DMA address in sofaware. We use SOPC-NIOSII EDA / SOPC System platform of Hum-Heng Technology co.

中文摘要本论文实验目标是在於利用SOPC-NIOSII EDA/SOPC系统平台来实现即时移动物体侦测的系统，影像输入透过CMOS Sensor接收影像的资料经过RGB格式的转换，再经过处理器处理影像侦测的运算，最后再将处里后的影像资料传送给VGA做即时的影像输出，我们使用DE2平台的测试范例程式转换在SOPC-NIOSII EDA/SOPC系统平台实验板来实现整个的硬体，我们将影像侦测系统分为硬体和软体二部份，硬体部分我们使用Verilog硬体描述语言修改撰写，利用SOPC Builder的自订IP产生我们所需的IP ，在COMS Sensor到FPGA跟FPGA到VGA中间我们需要一个interface来进行连接，经由Quartus II来合成产生*。sof的烧入档，然后利用SOPC-NIOSII EDA/SOPC系统平台专用的USB BLASTER来烧入到FPGA上，软体部分我们使用NIOSII IDE来定址我们DMA位址，主板我们采用华亨科技公司的SOPC-NIOSII EDA/SOPC系统平台。

Based on the predecessors experimental studies on the gaseous diatomic compounds of gold and on the chloride systems, this study approaches the volatile transport of gold related to organic matter in a new experimental system.

在前人已证明金呈气态双分子及金可在氯化物体系中迁移的实验基础上，本项成果在新的实验研究领域对金呈气相富集与有机质关系进行了探讨。

Thirty-six rats ,weighing(250±10)g, were randomly divided into normal group, experimental group and control group.Orthodontical devices were put between the upper incisor teeth and dens molaris in both experimental group and control group.The corrective force was adjusted to 60g.Salvia miltiorrhiza combination was implanted to each rat in the experimental group every day.The animals of both experimental group and control group were killed at 7,14 and 21 days.The upper dens malarias and periodontal tissue slices were observed under the light microscope and transmission electro microscope,and the X-ray dental films were taken and measured with digitization dental scanning apparatus and its software.

以36只体重(250±10)g的雄性大鼠为样本，随机分为正常组、实验组和对照组，设定不同浓度丹参复合膜，以同体对照方式在正常组进行体内植入实验，在2周内观察不同浓度丹参的牙周组织诱导作用，寻找最佳应用浓度；在实验组和对照组的上切牙与磨牙之间隙安装正畸装置，建立大鼠磨牙移动实验模型，矫治力的大小为60g；实验组每日每只体内植入丹参复合生物膜，两组动物于正畸加力7、14、21d，分三批处死；处死后立即切取双侧上颌磨牙及牙周组织制取标本，制片透射电镜和光镜观察；拍摄X线牙片，用数字化牙科扫描仪及软件对其进行测量分析。

The corrective force was adjusted to 60g.Salvia miltiorrhiza combination was implanted to each rat in the experimental group every day.The animals of both experimental group and control group were killed at 7,14 and 21 days.The upper dens malarias and periodontal tissue slices were observed under the light microscope and transmission electro microscope,and the X-ray dental films were taken and measured with digitization dental scanning apparatus and its software.Result:The most fitting concentration of combined biological membrane was 0.80g;the speed of the remodeling of the periodontal tissue at the compression side in the experimental group was faster than that of the control group.

以36只体重(250±10)g的雄性大鼠为样本，随机分为正常组、实验组和对照组，设定不同浓度丹参复合膜，以同体对照方式在正常组进行体内植入实验，在2周内观察不同浓度丹参的牙周组织诱导作用，寻找最佳应用浓度；在实验组和对照组的上切牙与磨牙之间隙安装正畸装置，建立大鼠磨牙移动实验模型，矫治力的大小为60g；实验组每日每只体内植入丹参复合生物膜，两组动物于正畸加力7、14、21d，分三批处死；处死后立即切取双侧上颌磨牙及牙周组织制取标本，制片透射电镜和光镜观察；拍摄X线牙片，用数字化牙科扫描仪及软件对其进行测量分析。

For a big chunk of credit-card losses; the number of filings (and thus charge-off rates) would be rising again, whether

年美国个人破产法的一个改动使得破产登记急速下降，而后引起了信用卡大规模的亏损。

Eph. 4:23 And that you be renewed in the spirit of your mind

弗四23 而在你们心思的灵里得以更新