基于Mesh网的矿工心电信号无线监测系统研究

在矿难事故发生后实时监测被困矿工的生命体征,能够给营救工作提供重要的信息参考,因此设计了一款基于Mesh网的矿工心电信号无线监测系统.通过ADS1292心电检测模块对矿工的实时心电信息进行监测,然后将心电数据经过STM32F103单片机处理后通过OLED屏显示出来.同时,处理后的数据还可以通过无线组网模块发送至上位机进行显示,从而实现对井下采煤工人生命体征进行远程监测的目的.测试结果表明:该系统可以准确获取矿工心电信号波形,实测心率误差不超过4％,具有良好的应用前景和实用价值.     

基于熵评价模态分解的雷达信号双谱特征识别

针对在低信噪比下雷达信号调制识别准确率低、抗噪性差的问题, 提出一种基于熵评价模态分解和双谱特征提取的识别方法。利用双谱可以抑制高斯噪声的特点, 分析了在低信噪比下进行信号调制识别的可行性并引入了噪声项。由于噪声项的干扰, 双谱在0 dB以下时, 噪声抑制效果变差, 提出了基于信息熵评价的经验模态化分解对信号进行预处理, 提高信噪比。最后, 设计了卷积神经网络分类器, 实现对不同调制类型信号的识别。仿真实验结果表明, 本文方法相比传统方法具有良好的抗噪性, 能够在低信噪比下对不同类型信号进行有效识别。     

2017—2019 年北京地区实验动物质量抽检结果分析

摘要:目的 比对分析 2017—2019 年北京地区实验动物微生物及遗传质量监测结果,为实验动物产业发展提供参考。 方法 按照国家和地方现行实验动物检测标准,对北京地区实验动物生产单位进行抽检,并发布检测报告。按照报告数据,对此阶段小鼠、大鼠、豚鼠、地鼠、兔、犬、猴和小型猪共 8 个品种的实验动物按照品种、等级、单位等进行分类,分析质量问题,并与 2014—2016 年同期实验动物质量比对,分析变化趋势。 结果 2017—2019 年分别抽检动物 144、131 和 135 批次,检出不合格批次分别为 30、15 和 17 批。 不合格主要因素为兔、犬及猪免疫不达标(20 批) ,病原感染 20 批,未发现遗传变异。 与 2014—2016 年同期相比,未检出遗传问题相同,免疫不达标状况好转,但病原感染出现上升。 结论 通过质量分析比对,能够为实验动物产业健康发展提供数据支持。     

民族高校工商管理专业实践教学体系创新研究

围绕工商管理专业培养具有较强实践能力和高素质管理人才的目标,分析当前实践教学中的误区,通过构建全社会参与的工商管理专业人才实践教学社会网络,建立贯穿大学四年学习全周期的五大实践教学培养体系,对工商管理专业学生进行基础素养实践能力和专业素养实践能力培养,探索工商管理专业人才实践能力培养模式和体系。     

深水铺管船的动力定位能力评估系统

为解决评估铺管船作业能力的难题,提出一种适用于评估铺管船动力定位能力的方法,开发了动力定位能力评估程序系统,并针对高海况环境条件设计了优化的辅助作业方案.采用数值计算方法对铺管船作业期间的平均二阶力、风载荷以及流载荷进行仿真计算,建立了环境载荷与动力定位系统提供的推力之间的平衡关系,给出了用于评估铺管船动力定位能力的系统模块,采用动力定位能力包络线的方式表达动力评估结果.在高海况作业中给出安全建议,即采用辅助拖轮作用于船舶适当位置以增强动力定位能力,从而降低工程作业风险.     

分级事权下县级国土空间规划的编制

立足现行“县 乡镇 村”三级行政构架，我国县级国土空间规划的编制需要注意几个关键点:一是在规划层级方面，除个别城乡高度融合的县市可按全域“一个层级”编制规划外，其他大部分县市仍应执行“全域 中心城区”两个层级；二是除高度城市化地区可将县级 乡镇级规划合并编制外，其他大部分县市宜按两个或多个乡镇联合开展规划编制，给乡镇预留更多的自由裁量权；三是县级规划应重点加强对县域村庄总量控制、分类引导、刚性传导等方面的顶层设计，其他事权可交由下层级规划落实。建议尽快出台国土空间规划相关法律法规和部门规章，规范各级国土空间规划成果编制，强化国土空间规划的指导约束作用。     

氧化还原介体催化强化污染物厌氧降解研究进展

 由于厌氧生物处理技术具有产生剩余污泥少、可回收能源等优点而被广泛用于处理各种有机污染物，尤其在有毒、有害、难降解污染物的去除方面取得了良好的效果。然而，厌氧生物法的处理速率通常比较低，而氧化还原介体可通过自身不断的氧化和还原来传递电子，提高电子在氧化还原反应过程中的传递速率，从而促进污染物高效厌氧降解。醌类物质和腐殖酸是应用较多的氧化还原介体，在催化难降解污染物降解方面取得了一定效果。讨论了氧化还原介体的特点、作用机制，并总结了其对偶氮染料厌氧脱色、反硝化和多氯联苯厌氧降解的强化作用，提出了氧化还原介体未来的研究方向。     

工程实践中的体系与系统

 介绍了国际上通行的体系概念，通过实例阐述了常见的体系类型，从多个维度描述了系统与体系的区别，根据实践总结，提出体系与系统的核心界定准则，并结合工程实践进行了详细描述。     

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.

     

Study on the Centralization Strategy of the Blood Allocation Among Different Departments within a Hospital

By far, the researches on how to distribute blood products among different departments in hospital have not been further studied, though the problem of blood shortage and wastage that caused by improper blood allocation is severe, which may endanger patient’s lives and impose considerable costs on hospitals. In order to solve this problem, this paper mainly studies on how to distribute the blood items among different departments within a hospital and investigates the allocation approach with the novel management method by centralizing the inventory of several different departments. By integrating the blood inventory requirements of some departments, the hospital could reduce the rate of blood shortage and wastage effectively, release the pressure of the occupancy of resources and reduce the bullwhip effect of blood products. This paper illustrates the centralization principle in hospital and formulates the mixed integer programming model to work out the optimal allocation network scheme and the optimal inventory setting for every department. And the results of the numerical example demonstrate that this centralization method could considerably reduce blood shortage and wastage in hospital by about 72% and 90% respectively. Furthermore, it could decrease the total cost by about 108,540 RMB a month on blood supply chain management in the hospital and improve the effect of some certain surgeries by transfusing the fresh blood to patients.