互联网专车服务对出租车行业垄断的影响

通过数学建模方法可知，由于出租车公司和政府部门追求垄断利润，出租车司机和消费者的福利减少，因此，对消费者和司机来说，出租车行业垄断确实是一种伤害.互联网专车服务以低廉的价格和优质的服务，是打破出租车行业垄断的有力工具.从模型分析揭示的结果可知：传统的出租车行业必须对司机、消费者、公司和政府间的利润分配制度进行深层次的改革.只有这样，才能建立一个和谐的出租车服务体系.     

黄色黏虫板诱杀技术在辣椒蚜虫绿色防控上的应用

进行了黄色黏虫板防控和诱杀辣椒(Capsicum annuum)蚜虫(Aphidoidea)成虫的试验。结果表明,黄色黏虫板对辣椒蚜虫成虫防控和诱杀效果较显著,每667 m2挂板21块,放置高度1 m,方向朝南的诱杀效果最好。它可减少药剂使用次数,对控制蚜虫种群密度具有显著作用和良好的应用前景。     

汽车侧面碰撞中乘员约束系统的可靠性优化

在汽车侧面碰撞中，约束系统对降低乘员的伤害起到非常重要的作用.本文采用MADYMO仿真分析软件，建立某车型侧面碰撞的约束系统仿真模型；考虑了髋部推动块的压溃力、气囊起爆时间、气体质量流量和气袋排气孔面积对乘员损伤的影响，建立了乘员损伤指标的响应面模型；基于蒙特卡罗随机模拟，进行了侧面碰撞乘员约束系统的可靠性优化.结果表明，优化后的约束系统设计方案满足可靠性目标要求.     

我国茶园机械化作业模式研究

为从宏观层面探索我国茶园机械化发展道路,使我国茶园机械化早日走出步履维艰的发展困境,深入分析了我国茶园机械当前的应用推广情况,存在的问题以及最近研究进展。通过对我国茶园机械化发展现状的深层次分析,发现除技术原因外,茶园分布广而散,地理地形复杂,是阻碍我国茶园机械化发展的重要因素。基于此,提出"分形而治"的机械化作业模式与理论,从根源上肃清我国茶园机械化盲目发展的局面,促使其从此迈入健康的发展道路,对加快我国茶园机械化发展意义非凡。     

红壤旱地芝麻防早衰叶面调控剂筛选研究

研究结果表明,速效肥料、生长调节剂及抗病药剂对保持芝麻生长中后期的正常生长都能起到积极作用。"磷酸二氢钾+硝酸铵+腐植酸+赤霉素"配制能有效防控红壤旱地芝麻早衰,在此配方基础上,添加代森锰锌能对防控芝麻叶部及茎部病害起到一定的作用,从而增强了红壤旱地上芝麻的抗早衰能力。     

基于嵌入式操作系统的数字音频播放器优化控制

基于经济租金理论和商业模式创新特点，考量企业家商业模式创新的动因、企业家商业模式创新中的能力构成以及创新绩效。运用结构方程模型对相关假设进行实证检验，结果表明，企业家发现机会的能力、承担风险和不确定性的能力对商业模式创新行为具有显著正向影响，且企业家商业模式创新行为对创新绩效的正向影响显著，商业模式创新行为实现了经济租金的获取。     

锰胁迫下鸡眼草的富集特征及生理响应

为探明植物对锰胁迫的耐受性机制,以采自重金属污染区与非污染区的鸡眼草为试验材料,在不同锰浓度胁迫下［0 （对照）、1000、5000、10000、15000、20000 μmol·L^-1］ 开展盆栽试验,比较研究锰胁迫对两种来源鸡眼草表型、生理生化特性及锰积累特征的影响。结果表明：随着锰浓度的升高,1） 两种来源鸡眼草的根干重、芽干重、根冠比均呈降低的趋势;当锰浓度达5000~20000 μmol·L^-1时,与对照相比,污染区、非污染区鸡眼草的芽干重分别下降4.34%~27.71%与16.33%~49.77%,根干重分别下降19.00%~66.06%与27.90%~77.54%,污染区下降幅度均较非污染区的小;2） 两种来源鸡眼草的叶绿素、可溶性糖、脯氨酸含量及超氧化物歧化酶（SOD）、过氧化物酶（POD）活性均呈先升后降的趋势,可溶性蛋白含量逐渐下降,丙二醛（MDA）含量则逐渐升高;3） 两种来源鸡眼草根、茎、叶的锰含量均增加;锰浓度为20000 μmol·L^-1时,污染区和非污染区鸡眼草的叶锰含量分别为对照的16.53和13.41倍。因此,污染区鸡眼草锰耐受能力及富集能力均较非污染区鸡眼草高,较高的抗氧化酶活性是其耐受高锰胁迫的重要生理机制。     

猪戊型肝炎病毒ORF3蛋白影响HepG2细胞核黄素代谢的lncRNA-mRNA调控网络的鉴定

为初步鉴定并挖掘出猪戊型肝炎病毒(Hepatitis E virus,HEV)ORF3蛋白影响HepG2细胞核黄素代谢信号通路的lncRNA-mRNA调控网络,本试验通过构建腺病毒过表达载体,制备高滴度过表达腺病毒,介导猪 HEV-ORF3在HepG2细胞中实现过表达。Western blotting检测ORF3蛋白过表达成功后,运用lncRNA高通量组学测序,筛选出差异表达的lncRNA并进行靶向差异基因预测,对lncRNA靶向差异基因进行GO功能和KEGG通路富集分析,初步鉴定出与核黄素代谢信号通路相关的lncRNA-mRNA调控网络。Western blotting结果显示,在约为12 ku处出现目的条带,说明成功实现腺病毒介导猪HEV-ORF3在HepG2细胞中过表达。lncRNA高通量组学测序结果显示,共发现102个显著差异表达lncRNAs表达量上调,80个显著差异表达lncRNAs表达量下调。GO功能和KEGG通路富集分析显示,初步挖掘出lncRNA(MSTRG.13995.2)和lncRNA(MSTRG.1960.1)可能是与核黄素代谢信号通路相关的显著差异表达lncRNA,分别通过顺式调控其靶向基因APC-5和FLAD1来影响核黄素代谢信号通路。本试验初步鉴定出lncRNA(MSTRG.13995.2)-APC5和lncRNA(MSTRG.1960.1)-FLAD1可能是影响HepG2细胞核黄素代谢信号通路的lncRNA-mRNA调控网络。     

Expression Analysis of THBS3 Gene in Different Tissues and Skeletal Muscles at Different Periods from Landrace and Tongcheng Pigs

To study the expression pattern of THBS3 gene in different tissues and during skeletal muscle development, the THBS3 gene expression in different tissues and skeletal muscles during prenatal periods (33, 45, 65, 70 and 90 d) and postnatal periods (0, 9, 30, 60, 120 and 160 d) from Landrace and Tongcheng pigs were detected by Real-time quantification PCR.The results showed that THBS3 gene widely expressed in all tissues examined, exhibiting similar spatial expression patterns with expression peaks in lung in both pig breeds except in stomach and intestine.Moreover, although THBS3 gene showed a significant higher expression level in gestation than after birth in Landrace and Tongcheng pigs (P<0.05), it exhibited different expression patterns between Landrace and Tongcheng pigs, the expression peak was detected at gestation day 45 in Landrace pig, while was detected at gestation day 65 in Tongcheng pig.The results suggested that THBS3 gene involved in skeletal muscle growth and development in pigs, as well as the regulation of asynchronization of skeletal muscle development in different pig breeds.     

Establishment of a Duplex Real-time RT-PCR Assay for the Differential Detection of Nipha Virus and Highly Pathogenic Porcine Reproductive and Respiratory Syndrome Virus

To establish a rapid,sensitive and specific assay for the differential detection of Nipah virus (NiV) and highly pathogenic porcine reproductive and respiratory syndrome virus (HP-PRRSV),a duplex Real-time RT-PCR was developed with specific primers and probes targeting to the special sequences of NiV M gene and HP-PRRSV nsp2 gene by optimization of reaction conditions.The performance of the assay was linear ranging from 4.6×10¹ to 4.6×10⁷ copies/μL for RNA standard control of NiV M (NiV-M-RNA) and from 4.1×10¹ to 4.1×10⁸ copies/μL for RNA standard control of HP-PRRSV nsp2 (HP-PRRSV-nsp2-RNA),and detection limits of the assay was 46 copies for the NiV-M-RNA and 4.1 copies for the HP-PRRSV-nsp2-RNA,respectively.The coefficients of variation (CVs) of both inter-assay and intra-assay repeatability were less than 2.0%,showing good repeatability.The assay was able to specifically detect NiV and HP-PRRSV simultaneously without cross-reaction with classical swine fever virus (CSFV),porcine epidemic diarrhea virus (PEDV),swine influenza virus (SIV),porcine parvovirus (PPV),pseudorabies virus (PRV) and porcine circovirus type 2 (PCV2).Of the 236 samples from pigs for both NiV and HP-PRRSV detection by the established assay,all the samples were negative for NiV,8 samples were HP-PRRSV positive.In conclusion,this assay offers a useful approach for the differential detection of NiV and HP-PRRSV in clinical specimens from the pigs.