飞秒光纤光源的波分解复用 复用实验

为研究飞秒光源作为链路初始光源的可行性，使用阵列波导光栅（AWG）对265 fs光纤光源进行波分解复用 复用实验。实验光源波长为1 52765～1 56505 nm，通道数为48，通道间隔为080 nm。研究发现:在分波实验中，飞秒光纤光源经过AWG后，扫描谱线3 dB带宽为064 nm ，相邻通道串扰为2726 dB，比连续光源增大502 dB；在合波实验中，观察到AWG多端口端对宽带光源的波长选择作用，验证了AWG的色散特性，发现多光束的输出谱线总体轮廓未出现太大变形；在波分解复用 复用实验中，谱线最大损耗为251 dB，输出谱线轮廓和初始光谱基本一致，信号在传输过程中未出现明显失真，证明飞秒光源作为链路初始光源的可行性。     

基于盒维数的锚杆工作荷载无损检测研究

为研究锚杆工作荷载,应用了分形理论中的盒维数方法。根据一维杆波动理论,在锚杆外露端头安装一个自激式加速度传感器,利用锚杆无损检测加载试验台分级加载、检测标定测得锚杆-围岩相互作用体系在激发荷载作用下的速度响应,计算其加速度响应曲线的盒维数,拟合得出荷载-盒维数曲线,直观地判断锚杆工作荷载和锚固质量。     

唐代试律诗诗题用典与唐代祥瑞尚奇文化

唐代试律诗诗题对有关祥瑞及灵异之类典故的大量选用,不但体现了唐代统治者借祥瑞文化维护自身统治的治国策略,也表明了尚奇之风在唐代的盛行。     

单快拍相干信号自适应波束形成方法

针对低快拍条件下相干信号波束形成问题,提出一种单快拍相干自适应波束形成方法。首先,构造Duvall特征消除器滤除阵列接收信号中的期望信号,再利用空间平滑方法解相关。然后,依据Hung Tuner算法对平滑后的协方差矩阵进行Gram Schmidt正交化,快速重构干扰信号子空间。最后,将静态权矢量在干扰子空间内的正交投影作为波束形成最优权矢量。该算法可有效避免协方差矩阵求逆和特征分解造成的复杂计算,且能降低由于期望信号泄露造成的子空间估计误差,在单快拍条件下性能良好。仿真分析验证了算法的优越性和理论分析的有效性。     

Simultaneous anti-windup synthesis for linear systems subject to actuator saturation

A synthesis method for global stability and performance of input constrained linear systems, which uses a linear outputfeedback controller and a static anti-windup compensator is investigated. Different from the traditional two-step anti-windup design procedure, the proposed method synthesizes all controller parameters simultaneously. Sufficient conditions for global stability and minimizing the induced L2 gain are formulated and solved as a linear matrix inequalities(LMIs) optimization problem, which also provides an opportunity to search for a better performance tradeoff between the linear controller and the anti-windup compensator.The well-posedness of the close-loop system is also guaranteed.Simulation results show the effectiveness of the proposed method.     

化工设备使用与保养技术分析

化工行业是我国工业发展的重要组成部分,是我国重要的产业类型。化工设备安全平稳运行是保证企业完成生产任务的重要因素,也是保证企业安全生产和利益最大化的基础。本文对化工设备产生故障的原因、故障出现的规律及保养维护措施等进行了探讨分析。     

普通话在线游戏学习系统的研究与应用

针对希望进一步掌握普通话口语学习的外国学习者,该研究提出了一种普通话游戏学习系统.系统的学习模式结合了计算机技术和语言学研究成果,打破了传统的教学模式的限制,对学习者进行实时评测,提供学习报告与口语学习的最终评定结果.结果表明,该系统能够较为有效地辅助外国学习者的普通话口语学习.     

The expansion of GPCR transactivation-dependent signalling to include serine/threonine kinase receptors represents a new cell signalling frontier

G protein-coupled receptor (GPCR) signalling is mediated through transactivation-independent signalling pathways or the transactivation of protein tyrosine kinase receptors and the recently reported activation of the serine/threonine kinase receptors, most notably the transforming growth factor-β receptor family. Since the original observation of GPCR transactivation of protein tyrosine kinase receptors, there has been considerable work on the mechanism of transactivation and several pathways are prominent. These pathways include the “triple membrane bypass” pathway and the generation of reactive oxygen species. The recent recognition of GPCR transactivation of serine/threonine kinase receptors enormously broadens the GPCR signalling paradigm. It may be predicted that the transactivation of serine/threonine kinase receptors would have mechanistic similarities with transactivation of tyrosine kinase pathways; however, initial studies suggest that these two transactivation pathways are mechanistically distinct. Important questions are the relative importance of tyrosine and serine/threonine transactivation pathways, the contribution of transactivation to overall GPCR signalling, mechanisms of transactivation and the range of cell types in which this phenomenon occurs. The ultimate significance of transactivation-dependent signalling remains to be defined but it appears to be prominent and if so will represent a new cell signalling frontier.