Oscillations of nonlinear partial difference systems

This paper studies the following two-dimensional nonlinear partial difference systems

     

Symmetric and Rees algebras of Koszul cycles and their Gröbner bases

In this paper we study the symmetric algebra S(E _i ) and Rees algebra R(E _i ) of the modules E _i of i-cycles of the Koszul complex associated with the sequence of indeterminates of a polynomial ring . For i=2 and i=n–2 we show that is a d-sequence on S(E _i ) and R(E _i ) and we determine Gröbner bases and Sagbi bases related to these algebras. Mathematics Subject Classification (2000):13A30, 13D02, 13H10, 13P10The second author is grateful to the National Natural Science Foundation of China for support.Part of this work was made while the third author was visiting the Fachbereich Mathematik und Informatik der Universität Essen, to which he would like to thank for its hospitality.     

求解平片裂纹问题的有限部积分与边界元法

本文利用位移的Somigliana公式和有限部积分的概念,导出了求解三维弹性力学中的任意形状平片裂纹问题的超奇异积分方程组,进而联合使用有限部积分法与边界元法对所得方程建立了数值法.为验证本文的方法,计算了若干数值例子的裂纹面的位移间断及裂纹前沿的应力强度因子,它们与理论值相比符合很好.     

临床试验(Ⅱ)

在本文的第Ⅰ部份，涉及了临床试验的内涵、研究中的偏性、困难与临床试验设计的进展．第Ⅱ部份主要涉及分析中的一些重要问题，其中包括：５，生存质量的测定；６，病人的依从性； ７， Ｍｅｔａ分析．     

闭壳层原子相关效应的多体理论计算：Ne原子基态相关能

对coupled-pair many-electron theory(CPMET)展开中的非线性四体效应采取了近似处理,用角动量图技术和两体函数方法得到了适用于一般闭壳层原子的径向微分方程。然后以X_a模型作为零级近似,通过迭代求解成功地计算了Ne原子基态的任意阶相相关能,从而说明至少对于闭壳层原子体系而言,用X_a模型作零级近似同样可以进行成功的多体理论计算。     

小间隙高放大多丝室及其放电机制

对以强猝灭气体工作的小间隙多丝室及其放电机制进行了研究,实验表明,因为工作在饱和模式区,这种室同时具有很高的气体放大和相当快的时间特性.文中探讨了放电机制,雪崩中空间电荷效应以及电离光子的产生和作用是重要的因素,而其中后一因素又受到强猝灭气体的抑制.     

美式期权定价中非局部问题的有限元方法

在本文中 ,我们关心的是美式期权的有限元方法 .首先 ,根据 [4 ]我们对所讨论的问题引进一个新奇的实用的方法 ,它涉及到对原问题重新形成准确的数学公式 ,使得数值解的计算可以在非常小的区域上进行 ,从而该算法计算速度快精度高 .进而 ,我们利用超逼近分析技术得到了有限元解关于 L2 -模的最优估计 .     

Unfolding Features of Bovine Testicular Hyaluronidase Studied by Fluorescence Spectroscopy and Fourier Transformed Infrared Spectroscopy

Chemical unfolding of bovine testicular hyaluronidase (HAase) has been studied by fluorescence spectroscopy and Fourier transformed infrared spectroscopy (FTIR). Thermodynamic parameters were determined for unfolding HAase from changes in the intrinsic fluorescence emission intensity and the formations of several possible unfolding intermediates have been identified. This was further confirmed by representation of fluorescence data in terms of ‘phase diagram’. The secondary structures of HAase have been assigned and semiquantitatively estimated from the FTIR. The occurrence of conformational change during chemical unfolding as judged by fluorescence and FTIR spectroscopy indicated that the unfolding of HAase may not follow the typical two-state model.