明清时代的鄱阳商业与商人

文章利用方志与墓志中的商业与商人史料,分析了明清时代鄱阳县本地商业状况与外来商帮构成,以及鄱阳商人的经营行业和商贸地域.透过商人的传记资料,可以看到士人为商人写传,大力肯定商人的志业,商人则高度认同士人所代表的儒学主流价值观;方志为商人立传,商人为桑梓与国家效力,体现的是士商之间、商人与国家和社会之间相得益彰、"美美与共"的良性互动.     

螺栓连接大变形梁非线性振动特性的实验研究

柔性机械臂、大型可展开天线等机械结构的动作精度受运动过程中大变形几何非线性和连接处接触非线性的影响十分显著。以含螺栓连接结构的大变形梁作为研究对象，针对动力学建模和振动特性开展了实验研究，通过数值计算验证了实验发现的非线性振动特性。搭建了含螺栓连接柔性大变形梁的实验台架，开展了敲击和正弦激振的实验测试。实验结果表明，螺栓连接的柔性梁较连续梁的（无螺栓连接）模态频率降低，阻尼增加，反映出随着激励能量增大，模态频率降低的非线性模态特征。改变螺栓连接位置会显著影响结构的模态频率，其变化规律可由求解线性矩阵特征值定性反映。     

阳极修饰对微生物燃料电池性能的影响

利用PW12/rGO复合材料负载于碳布表面制得PW12/rGO修饰阳极并构建单室空气阴极微生物燃料电池(microbial fuel cells,MFC),考察了PW12/rGO修饰阳极对MFC产电和高氯酸盐(ClO4-)还原性能的影响,并通过对阳极表面形态及其电化学特性的分析,探讨了PW12/rGO修饰阳极改善MFC产电性能的机理.结果 表明,当ClO4-浓度为700 mg/L时,PW12/rGO修饰阳极MFC的最大输出电压和ClO4-平均去除速率分别为200.18 mV和1.15 kg/(m3·d),分别是空白阳极MFC的4.4倍和1.06倍;扫描电镜(SEM)表征显示,PW12/rGO修饰阳极表面附着的微生物量远高于空白阳极;Tafel曲线、循环伏安曲线(CV)和交流阻抗谱(EIS)测试表明,PW12/rGO修饰阳极较空白阳极具有更高的交换电流密度、CV电活性面积以及更低的电荷转移电阻.PW12/rGO修饰阳极提高了阳极电子产量和电子传递速率,进而改善了MFC的产电性能.     

富水砂层大断面暗挖隧道施工地层演化

对于施工环境复杂的暗挖隧道工程,科学合理掌握施工地层演化过程是安全施工的前提.以北京地铁12号线光熙门站—西坝河站区间富水砂层大断面暗挖隧道工程为研究背景,借助FLAC3D有限差分软件,对工程设计施工方案进行模拟,得到了施工过程中地层孔隙水压力、地层沉降损失演化过程,并与现场监测数据进行对比验证,为工程施工规避风险源提供参考.结果 表明:施工掌子面孔隙水压力集中位置主要在暗挖隧道上方注浆形成的"注浆拱"拱顶以及断面未注浆范围;隧道施工过程中,沿施工掘进方向在施工掌子面前、后10 m到掌子面位置范围内,是发生涌水关键位置;地层沉降值经历了由沿中轴线对称分布到集中在中轴线位置处的变化过程,最后沉降值沿中轴线对称分布,导洞1施工掌子面处地表沉降值稳定在12 mm左右;初期支护拱顶沉降以及拱脚水平收敛均分别在45、30 d达到稳定;现场反馈的施工信息与模型计算地层演化过程相吻合,计算结果可为富水砂层大断面暗挖隧道施工方案的选择提供参考.     

梯形微通道气液分相强化换热实验研究

针对微通道换热器强化沸腾换热,提出分段式梯形换热结构,该结构可实现气泡在表面张力驱动下间断性流向通道两侧,保持中间加热区为液体,实现气液分相流动,进而强化沸腾换热性能。采用无水乙醇为工质,实验研究直肋和梯形结构铜基表面在热流密度为160~320 kW/m²和工质流量为0.4~2.0 g/s时壁温、换热系数等参数变化规律。结果表明：在饱和沸腾区,梯形分相结构可有效实现气液分离,进而降低壁面温度,大幅提高换热系数；如在25 mm位置处,5段结构换热系数比平行结构换热系数提高了60.4%；在单相加热区,换热面积为主要影响因素,直肋结构换热系数略大,但换热系数比饱和沸腾时小一个数量级。平均换热系数分析得到5段结构微通道比平行结构微通道提高了53.8%,可见分段式结构可实现气液分相流动,有效提高沸腾换热的平均换热系数,增强整体换热能力。     

烟支硬度检测结果影响因素分析

为探究烟支硬度检测结果的影响因素,对烟支物理指标检测方案进行优化,提升卷烟质量监督水平.本试验以3类卷烟泰山(东方)为试验材料,分别设计不同检测方案、挡烟板位置、预压时间、压缩时间、压缩速度、环境湿度、贮存时间来对烟支硬度进行测定.烟支检测全项时硬度明显高于单独检测出的硬度;随挡烟板位置的增加,烟支硬度检测值先下降再上升;预压时间、压缩速度对烟支硬度检测结果影响不显著;不同的测试环境湿度会引起烟支水分变化,进而导致烟支硬度检测值产生变化;1个月内硬度不会发生明显变化,但是随着贮存时间延长而增长.应适当优化烟支物理指标检测顺序或方案,设置挡烟板位置为距离接嘴端55 mm,降低测定环境湿度为60％±2％,减少烟支贮存时间或控制贮存环境湿度,及时维护测定设备,以提升质量监督水平.     

基于负温度系数热敏电阻多通道高精度可穿戴式体温采集系统的设计

体温通常用于筛查传染病、监测治疗.为了确定皮肤表面温度.通过恒压式测温电路测电阻的方法,研究设计了可穿戴式多点体温监测系统,以STM32F103C8T6芯片为核心处理器,负温度系数热敏电阻(negative temperature coefficient,NTC)作为感温元器件,ADS1256芯片为温度信号调理器,蓝牙模块为无线传输单元,用LABVIEW设计上位机界面.热敏电阻及分压电阻构成的恒压式电桥电路进行8路温度数据的采集,24bits超高精度模数转换模块配置差分输入对模拟信号进行放大、滤波以及模数转换;转换后的数据在单片机中处理和运算;最终通过蓝牙将数据传至上位机.采用Stein-hart方程的四阶公式对热敏电阻作线性补偿.从软件和硬件上减少环境干扰和体温分布不均的影响.分析了温传感器的温度测量误差.实验结果表明,测量系统分辨率达0.01℃,测温准确度可达±0.02℃.此设计方案,具有较高的稳定性和精确性;并且该电路结构简单、体积小、低功耗,可用于需要精密测体温场合.     

Side-Channel Attacks in a Real Scenario

Existing Side-Channel Attacks(SCAs) have several limitations and, rather than to be real attack methods,can only be considered to be security evaluation methods. Their limitations are mainly related to the sampling conditions, such as the trigger signal embedded in the source code of the encryption device, and the acquisition device that serves as the encryption-device controller. Apart from it being very difficult for an attacker to add a trigger into the original design before making an attack or to control the encryption device, there is a big gap in the capacity of existing SCAs to pose real threats to cipher devices. In this paper, we propose a new method, the sliding window SCA(SW-SCA), which can be applied in scenarios in which the acquisition device is independent of the encryption device and for which the encryption source code requires no trigger signal or modification. First,we describe the main issues in existing SCAs, then we theoretically analyze the effectiveness and complexity of our proposed SW-SCA —a method that can incorporate a sliding-window mechanism into almost all of the existing non-profiled SCAs. The experimental results for both simulated and physical traces verify the effectiveness of the SW-SCA and the appropriateness of its theoretical complexity.     

双辊薄带连铸低碳微合金钢的铸态组织

采用双辊薄带连铸技术制备了低碳微合金钢薄带，利用OM，SEM和TEM对铸态凝固组织、室温组织、析出及位错进行观察和分析.结果表明:低碳微合金钢铸带的凝固组织中二次枝晶间距约为12~15μm，相对于传统厚板坯和薄板坯连铸，铸带组织得到了明显细化.铸带的原奥氏体晶粒尺寸比较粗大，约为250~410μm，其组织由魏氏铁素体、珠光体和不规则铁素体组成.铸带组织中存在纳米级TiC析出和短棒状的渗碳体.TiC析出没有被薄带连铸的凝固过程及二次冷却过程明显抑制.铸带组织由于铸轧力及二次冷却速率不均匀导致大量位错的产生.     

Defining G protein-coupled receptor peptide ligand expressomes and signalomes in human and mouse islets

Introduction

Islets synthesise and secrete numerous peptides, some of which are known to be important regulators of islet function and glucose homeostasis. In this study, we quantified mRNAs encoding all peptide ligands of islet G protein-coupled receptors (GPCRs) in isolated human and mouse islets and carried out in vitro islet hormone secretion studies to provide functional confirmation for the species-specific role of peptide YY (PYY) in mouse islets.

Materials and methods

GPCR peptide ligand mRNAs in human and mouse islets were quantified by quantitative real-time PCR relative to the reference genes ACTB, GAPDH, PPIA, TBP and TFRC. The pathways connecting GPCR peptide ligands with their receptors were identified by manual searches in the PubMed, IUPHAR and Ingenuity databases. Distribution of PYY protein in mouse and human islets was determined by immunohistochemistry. Insulin, glucagon and somatostatin secretion from islets was measured by radioimmunoassay.

Results

We have quantified GPCR peptide ligand mRNA expression in human and mouse islets and created specific signalomes mapping the pathways by which islet peptide ligands regulate human and mouse GPCR signalling. We also identified species-specific islet expression of several GPCR ligands. In particular, PYY mRNA levels were ~ 40,000-fold higher in mouse than human islets, suggesting a more important role of locally secreted Pyy in mouse islets. This was confirmed by IHC and functional experiments measuring insulin, glucagon and somatostatin secretion.

Discussion

The detailed human and mouse islet GPCR peptide ligand atlases will allow accurate translation of mouse islet functional studies for the identification of GPCR/peptide signalling pathways relevant for human physiology, which may lead to novel treatment modalities of diabetes and metabolic disease.