对象关系数据库系统模型及映射规则

在业务逻辑层和关系数据库的物理存储结构中间增加一个O R代理层,提出了一个对象关系数据库系统的三层模型,并对系统模型的各个层次进行了详细的功能设计和分析;总结出了代理层O R映射的4条基本规则,并对各自的优缺点进行了比较.结果表明,该模型在实际应用中存在有效性.     

关于强增生型变分包含问题解的Mann型迭代法

研究P-一致光滑的实Banach空间（1〈P≤2）中一类强增生型变分包含问题解的Mann型迭代逼近问题．在仅假设强增生映象的连续性下，利用徐宗本教授等人（1991年）给出的对偶映象L的HSlder连续性，证明了具误差的Mann迭代法强收敛到这类变分包含的唯一解．     

基于分数阶傅里叶变换的OFDM系统峰均比探讨

介绍了基于分数阶傅里叶变换的正交频分复用系统,推导了该系统中峰均功率比公式.探讨了该系统中使用选择映射法降低峰均比.在不同的分数阶域信号能量的聚集性不同,则其峰均比就不同;通过计算机仿真分析得到了在不同的分数阶数琢情况下系统的累积分布函数曲线,并与基于FFT的系统进行比较,实验结果表明当琢取最优值时,系统的峰均比互补累积函数性能优于基于FFT的系统性能.     

面向集群制造的注竣机开放式模块化设计技术

通过对集群制造系统结构特点的分析，提出了基于产品技术分割和技术模块价值选择的开放式模块化产品设计方法．该方法运用结构映射这一基于技术的功能和基于设计结构矩阵的技术单元聚类，实现了合理的产品技术分割；通过基于量化设计结构矩阵的技术结果关联分析和技术控制力评价实现了科学的技术模块选择；进而形成了面向集群制造的开放式产品模块化设计方法．最后以我国沿海注塑机企业集群为例，阐述了面向集群制造的开放式产品模块化方法的应用．     

企业应树立正确的人才观

分析了传统人才观念存在的误区,指出在市场经济条件下,企业要适应时代要求,必须树立人才范围的开放性观念、人才鉴别的实践性观念、人才评价的合理性观念、人才能力的相对性观念、人才管理的创新性观念、人才出于团队的观念等六大观念。     

空防对抗中战场态势综合评估的一种新方法

以防空作战实际需要为出发点,从作战指挥的角度对战场态势评估问题进行了深入研究。首先给出了战场态势的一种全新定义,提出了空袭态势和防空态势的概念,将影响态势的因素分为两类,一类为静态因素,一类为动态因素。详细给出了影响空袭态势和防空态势的静态因素、动态因素指标体系,并提出了确定因子表征值的一种新方法,它将因子表征值与因子属性值相区分,定义表征值是属性值对模糊概念的隶属度。在此基础上建立了基于模糊概念层次分解的战场态势综合评估模型。该成果已被用于指挥自动化系统中,为指挥员掌握战场全局以及战役进程提供很好的支持。     

机载脉冲多普勒雷达回波信号模拟

回波信号作为雷达信号处理之源,它的模拟对研究雷达系统仿真具有非常重要的实际意义。在研究雷达回波特性的基础上,获得雷达回波信号的准确表达式,采用映象法将地面分成大杂波单元和小杂波单元,对各小杂波单元产生的回波采用矢量相加以求得相干视频信号,计算整个距离环的回波获得完整的雷达回波信号。最后的仿真结果证明了计算的正确性。     

Mapping of the rice （Oryza sativa L.） thermo-sensitive genic male sterile gene tms5 with EST and SSR markers

VELOPING“TWO-LINE”HYBRID RICE.THE POLLEN FERTILITY OF TGMS IS REGULATED BY THE TEMPERATURE OF ENVIRONMENT.THE POLLENS OF TGMS LINES ARE STERILE WHEN THE ENVI-RONMENT TEMPERATURE IS ABOVE A CRITICAL POINT,BUT FERTILE BELOW THIS POINT.SO FAR,A NUMBER OF T…     

Strategy for the mapping of interactive genes using bulked segregant analysis method and Mapmaker/Exp software

A qualitative trait is usually controlled by a single gene, but it may be sometimes controlled by two or even more genes. This phenomenon is called gene interaction. Rapidly searching for linked mo- lecular markers via bulked segregant analysis (BSA) and then constructing regional linkage map with Mapmaker/Exp has become a common approach to mapping single major genes. However, methods and computer programs developed for mapping single major genes cannot be simply applied to interactive genes because the genetic patterns of gene interac- tions are quite different from that of single-gene in- heritance. Up to now, experimental methods for quickly screening molecular markers linked to inter- active genes and statistical methods and corre- sponding computer softwares for simultaneously analyzing the linkage relationships of multiple mo- lecular markers to an interactive gene have not been available. To solve this problem, in this paper, we propose a strategy for mapping interactive genes using BSA and Mapmaker/Exp. We demonstrate that all interactive genes can be mapped by the 'BSA Mapmaker/Exp' strategy using F2 generation (in a few cases, F3 generation is also needed). As BSA and Mapmaker/Exp have been broadly used in gene mapping studies and are well known by many re- searchers, the strategies proposed in this paper will be useful for practical researches.     

Genetic analysis and molecular mapping of a presenescing leaf gene psll in rice （Oryza sativa L.）

A rice psl1 （presenescing leaf） mutant was obtained from a japonica variety Zhonghua 11 via radiation of ^60Co-γ in M2 generation. Every leaf of the mutant began to wither after it reached the biggest length, while the leaves of the wild variety could keep green for 25--35 d. In this study, genetic analysis and gene mapping were carried out for the mutant identified. The SSR marker analysis showed that the mutant was controlled by a single recessive gene （psl1） located on chromosome 2. Fine mapping of the psl1 locus was conducted with 34 new STS markers developed around psl1 anchored region based on the sequence diversity between Nipponbare and 93-11. The psl1 was further mapped between two STS markers, STS2-19 and STS2-26, with genetic distances of 0.43 and 0.11 cM, respectively, while cosegregated with STS2-25. A BAC contig was found to span the psl1 locus, the region being delimited to 48 kb. This result was very useful for cloning of the psl1 gene.