湖南省水资源承载力综合评价研究

基于湖南省水资源现状,结合已有的水资源承载力评价指标体系,构建了囊括水资源、社会、经济和生态等4个方面20个指标因素的湖南省水资源承载力评价指标体系.运用TOPSIS模型对湖南省2005—2014年10年间的水资源承载力指标进行了定量分析,结合2014年湖南省各州市的水资源承载力结果,在时间和空间上对湖南省的水资源承载力进行了综合评价研究,并根据其结果给出了相关建议.结果表明,2005—2014年期间湖南省水资源承载力整体提升显著,水资源的开发利用有较乐观的发展潜力;2014年张家界、长沙和湘西自治州的水资源承载力优势最为明显,但水资源量与经济水平、人口分布等因素不协调.     

基于园林卓越人才培养的观赏植物组织培养课程实践改革

以园林专业卓越人才培养为目标,提出教学过程以应用与创新为导向,更新教学内容体系,探索引入项目式教学形式,调整考核方法.改革后的课程体系侧重学生实践动手能力与创新能力的培养,学生的学习主动性显著提高,在学生中反馈效果好,教学效果显著.     

接触网抗风可靠性研究现状及展望

介绍了接触网抗风可靠性研究的国内外现状;并分析了接触网风荷载作用下的失效形式、抗风可靠性的安全界限和破坏准则;对存在的难点及研究方向提出了几点建议。     

Granzyme B is recovered by natural killer cells via clathrin-dependent endocytosis

When they recognize a target cell, natural killer (NK) cells mount an attack to kill the target by exerting their cytotoxicity via the exocytosis of cytotoxic granules. Although the details of this process (which includes the movement of cytotoxic granules in the immune synapse and their fusion with the plasma membrane, releasing granzymes and perforin into the synaptic cleft) are relatively better understood, the post-exocytosis regulation of the process is still largely unknown. Here we show that a clathrin-dependent endocytosis stimulated by target cell occurs in NK92 cell line, which is closely correlated with granzyme B recovery. Inhibition of the endocytosis significantly attenuates the cytotoxicity of NK92 cells. The NK cell recovery of its released effector molecules, in turn, suggests that endocytosis may well play a key role in the post exocytosis regulation of immune cells.     

海杂波频谱的多重分形特性分析

本文主要研究海杂波频谱的多重分形特性并分析其影响因素．首先介绍了将多重分形理论引入到海杂波频谱分析中的理论基础,然后,采用X波段与S波段相参雷达实测数据验证海杂波频谱的多重分形特性,并采用多重分形去趋势起伏分析（MF-DFA）法对海杂波频谱进行多重分形特性分析、分析结果表明海杂波频谱是一种受长程相关性和概率分布共同影响的多重分形序列,并且频域多重分形参数广义Hurst指数对海杂波单元与目标单元具有一定的区分能力．此外．通过分析广义Hurst指数的影响因素还发现FFT时所采用的时间序列长度对广义Hurst指数影响相对较大,而FFT点数对其影响相对较小．     

月地高速再入返回飞行器信息系统设计与实现

探月三期月地高速再入返回飞行器由服务舱和返回器2个舱段组成,信息系统复杂,首先对信息系统的任务进行了分析,在此基础上提出了2层拓扑总线的互联方案、器内多子网自识别路由设计方案、链路层分层方案,脉冲调制编码(PCM)数据体制与高级在轨系统(AOS)数据体制统一设计方案,实现了多信源、多舱段信息管理与融合,提高了上行带宽利用率、器内数据路由和下行遥测灵活性和易扩展性,满足了飞行任务复杂工作模式下的需求,在轨飞行结果表明信息系统满足需求.     

Microautophagy: lesser-known self-eating

Microautophagy, the non-selective lysosomal degradative process, involves direct engulfment of cytoplasmic cargo at a boundary membrane by autophagic tubes, which mediate both invagination and vesicle scission into the lumen. With its constitutive characteristics, microautophagy of soluble substrates can be induced by nitrogen starvation or rapamycin via regulatory signaling complex pathways. The maintenance of organellar size, membrane homeostasis, and cell survival under nitrogen restriction are the main functions of microautophagy. In addition, microautophagy is coordinated with and complements macroautophagy, chaperone-mediated autophagy, and other self-eating pathways. Three forms of selective microautophagy, including micropexophagy, piecemeal microautophagy of the nucleus, and micromitophagy, share common ground with microautophagy to some degree. As the accumulation of experimental data, the precise mechanisms that govern microautophagy are becoming more appreciated. Here, we review the microautophagic molecular machinery, its physiological functions, and relevance to human diseases, especially in diseases involving multivesicular bodies and multivesicular lysosomes.     

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs

Schizophrenia is a complex disorder caused by both genetic and environmental factors. Using 9,087 affected individuals, 12,171 controls and 915,354 imputed SNPs from the Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium (PGC-SCZ), we estimate that 23% (s.e. = 1%) of variation in liability to schizophrenia is captured by SNPs. We show that a substantial proportion of this variation must be the result of common causal variants, that the variance explained by each chromosome is linearly related to its length (r = 0.89, P = 2.6 × 10(-8)), that the genetic basis of schizophrenia is the same in males and females, and that a disproportionate proportion of variation is attributable to a set of 2,725 genes expressed in the central nervous system (CNS; P = 7.6 × 10(-8)). These results are consistent with a polygenic genetic architecture and imply more individual SNP associations will be detected for this disease as sample size increases.     

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

We present an approximate conditional and joint association analysis that can use summary-level statistics from a meta-analysis of genome-wide association studies (GWAS) and estimated linkage disequilibrium (LD) from a reference sample with individual-level genotype data. Using this method, we analyzed meta-analysis summary data from the GIANT Consortium for height and body mass index (BMI), with the LD structure estimated from genotype data in two independent cohorts. We identified 36 loci with multiple associated variants for height (38 leading and 49 additional SNPs, 87 in total) via a genome-wide SNP selection procedure. The 49 new SNPs explain approximately 1.3% of variance, nearly doubling the heritability explained at the 36 loci. We did not find any locus showing multiple associated SNPs for BMI. The method we present is computationally fast and is also applicable to case-control data, which we demonstrate in an example from meta-analysis of type 2 diabetes by the DIAGRAM Consortium.     

基于NVH性能的排气系统悬挂点位置设计

基于平均驱动自由度位移（ADDOFD）理论,同时考虑车身侧与排气系统侧的NVH性能,以及各阶模态频率的不同权值的影响,对某车型排气系统吊点位置进行优化布置,并对布置吊点后的排气系统做声学稳健性分析。实际应用表明该设计方法能对汽车排气系统悬挂点选择提供可行性参考建议,在整车开发的初期,有效预测和控制车身结构的NVH性能。