选择性双向顺序压缩感知重建动态磁共振成像

压缩感知是一种新兴技术,该技术能够用远低于奈奎斯特采样频率采集的信号恢复出原始信号. 压缩感知成像方法大大提高了心脏磁共振成像的采集速度,已有的方法主要利用动态图像时间相关及心脏的周期性运动特征,如采用在时间维做傅立叶变换或求解每帧数据跟参考帧数据的差异获取稀疏数据,满足压缩感知重建的要求. 该文提出了选择性双向顺序压缩感知重建算法,利用相邻帧的差异更小的特点,获取更加稀疏的差异数据,同时利用动态图像的周期性,以目标函数积分为判据,在时间顺序和时间逆序两个方向选择效果更好的方向进行数据重建,降低图像伪影和噪声. 该选择算法,可以在不增加重建时间的情况下,选择双向顺序重建中最佳的结果. 该文对心脏磁共振图像数据进行了数据处理实验,并且跟传统压缩感知算法、参考帧差异方法及匙孔成像方法进行了比较. 结果表明：该方法无论从视觉效果还是从统计结果上,都有很大的改善.     

基于遗传优化的西太平洋副高异常活动年份的动力预报模型反演

基于2000–2010年NECR/NECP的500 hPa位势场资料, 用EOF时空分解方法和动力模型重构思想, 通过遗传算法的全局优化搜索和并行计算途径, 开展了500 hPa位势场动力预报模型反演, 建立了刻画副高活动的非线性动力预报模型, 实现了副高活动的中长期预报. 模型预报试验表明, 该模型对副高的中长期活动, 尤其是异常活动能够较好地描述和预报, 进而为副高等复杂天气系统的预报探索了新的方法思路. 关键词： 副热带高压 500 hPa位势场 动力模型反演 遗传算法     

Ni熔体凝固过程中临界晶核和亚临界晶核的分子动力学模拟

本文用分子动力学模拟研究了Ni熔体以不同冷速凝固后微观结构的演变规律, 并通过理论计算确定出了Ni熔体凝固后获得理想非晶的临界条件. 模拟结果发现冷速小于10¹¹ K/s时, Ni 熔体凝固后形成晶态组织; 冷速在10¹¹ K/s到10^14.5 K/s之间时, Ni熔体凝固后形成由晶态结构与非晶态结构组成的混合组织. 冷速小于10¹⁰ K/s, Ni 熔体凝固后形成的晶态组织具有fcc结构; 冷速在10¹⁰ K/s到10^14.5 K/s之间时, Ni熔体凝固后组织中的晶态由fcc和hcp结构层状镶嵌排列构成. 通过分析模拟结果和计算结果, 确定出了Ni熔体凝固后形成理想非晶的临界冷速为10^14.5 K/s. 并发现Ni熔体中临界晶核(冷速等于10^14.5 K/s)和亚临界晶核(冷速大于10^14.5 K/s) 均由fcc和hcp组成层状偏聚结构, 这表明Ni熔体中生长的晶体、临界晶核和晶胚的结构是相同的. 关键词： 分子动力学模拟 晶体团簇 临界冷速 结构     

场景轮廓的动态规划立体匹配算法

立体匹配算法是三维重建的关键步骤。由于实际场景中经常存在大片灰度相近的区域,稠密三维重建存在计算时间长、实时性差的问题。采用了场景的轮廓来重建场景的方法。基于场景中相邻点之间的视差应当是连续的假设,解决了轮廓在匹配时存在的"噪点"的问题,利用动态规划法对轮廓上各个点的视差进行约束以及求解最优解。由于提取轮廓后需要匹配的点数大为减少,用时可减少为原来的10%,得到与场景一致的轮廓视差图。     

乙醇在TiO2(110)表面光催化解离的动力学和超快电子动态学 (cited: 2)

采用实时双光子光电子能谱和时间分辨双光子光电子能谱技术分别研究了乙醇在该表面光催化解离的动力学和超快电子动态学过程. 通过测量与乙醇光催化解离相关的电子激发态随时间的演化,发现这个反应满足分型动力学. 乙醇在还原性TiO₂(110)上的光催化解离比在氧化性表面快,这归结于缺陷的存在降低了反应能垒. 这样一个反应的加速过程很可能是与缺陷电子相关的. 通过干涉双脉冲相关的测量,得到了乙醇-TiO₂界面电子激发态的超快动态学. 与甲醇的情况类似,这个电子激发态的寿命为24 fs. 激发态的出现为TiO₂和它周围环境的电子转移提供了一个通道.     

Order Parameter and Refractive Index of Cholesteryl Linoleate

Refractive indices of cholesteryl linoleate are determined at different temperatures and order parameters have been calculated in smectic and cholesteric phases.     

PHYSICAL PROPERTIES OF SOME NOVEL NEMATIC BIMESOGENS FOR THE FLEXOELECTRIC EFFECT

Abstract

In a chiral nematic liquid crystal, the flexoelectric effect consists of a fast and linear coupling with an applied electric field. One difficulty to overcome is the unwinding of the helix that occurs at higher fields due to dielectric coupling. The use of bimesogens, which possess very low molecular dielectric anisotropy can improve flexoelectric characteristics. New bimesogen compounds have recently been synthesised that exhibit switching angles of 45° for applied fields of about 9 V.μm^?1. In this paper, results from dielectric, electro-optic and dynamic light scattering measurements are reported for the new bimesogenic mixture. The dielectric anisotropy Δε changes sign with temperature and its values range between -0.2 and 0.3 for the temperature range studied. For Δε weakly positive, no electric field Freedericksz transition could be induced but Williams domains are observed instead. The large decrease in the bend elastic constant to viscosity coefficient ratio is attributed to a large increase in the bend viscosity coefficient.     

Effect of Alkyl Side Chain Length on Relaxation Behaviors in Poly(n-alkyl Acrylates) and Poly(n-alkyl Methacrylates)

Dynamic mechanical analysis (DMA) is used to investigate the effect of alkyl side chain length on the relaxation behavior of poly(n-alkyl acrylates) (PnAA) and poly(n-alkyl methacrylates) (PnAMA) above the glass transition temperature (T_g). Master curves and shift factors (log a_T) were obtained using the time–temperature superposition (TTS) principle. The log a_T curves of PnAA and PnAMA exhibit a dynamic crossover from one Vogel–Fulcher–Tammann–Hesse (VFTH) equation to another above T_g. The corresponding temperature was designated as the dynamic crossover temperature (T_c). It is found that T_c/T_g and the apparent activation energy (E_g) increases, e whereas the fragility index (m) decreases with increasing alkyl side chain length. Further analysis shows that m ∝ T_g, E_g∝ , and E_g∝ m² for both PnAA and PnAMA.     

High pressure stability of protein complexes studied by static and dynamic light scattering

The high pressure dissociation of hemocyanin prepared from the lobster Homarus americanus and casein micelles from cow milk were observed by in situ light scattering. The hemocyanin dodecamer dissociated via a hexamer into monomers in a two-step three-species reaction. The influence of ligands and the effector l-lactate on the dissociation behavior was investigated. While no effect by carbon monoxide after exchanging the ligand oxygen was observed, the addition of the effector l-lactate led to a decrease in the pressure stability. Due to a trimer intermediate which was found to be stabilized by l-lactate, the dissociation reaction in the presence of the effector was analyzed by a three-step four-species reaction. In the case of casein micelles, a two-step dissociation mechanism was found. The stabilizing interactions of casein micelles were identified and separated.     

非保守动力学系统Noether对称性的摄动与绝热不变量

基于非保守系统的El-Nabulsi动力学模型, 研究了非保守动力学系统Noether对称性的摄动与绝热不变量问题.首先, 引入El-Nabulsi在分数阶微积分框架下基于Riemann-Liouville分数阶积分提出的类分数阶变分问题, 列出非保守系统的Euler-Lagrange方程; 其次, 给出了Noether准对称变换的定义和判据, 建立了Noether对称性与不变量之间的关系, 得到了精确不变量; 最后, 提出并研究了该系统受小扰动作用后Noether对称性的摄动与绝热不变量问题, 证明了绝热不变量存在的条件及形式, 并举例证明结果的应用. 关键词： 非保守系统 El-Nabulsi动力学模型 对称性摄动 绝热不变量