生态技术在现代农业中的地位及其技术群构成

提出了现代农业的主要支撑技术包括生态技术、生物技术和管理技术,并分析了此三类支撑技术的相互关系;通过深入比较,指出生态技术在现代农业中应占主导地位,这是现代农业发展的内在要求,是中国生态环境现状的必然选择,是建立社会主义和谐社会的必然趋势;同时提出了生态技术群中应该重点发展的主要技术:立体农业技术、综合养殖生态技术、特色农业技术、多色农业技术、设施农业技术、农业综合节水技术、农业污染综合防治技术和无公害绿色农产品标准化生产技术等。     

Engineering Calculation Mode Based on Reformative B/S Architecture

Engineering designed mode has entered a new stage because of the development of network. New calculating system based on network appeared. By analyzing the common B/S architecture, this paper brings forward an reformative architecture based on Web services and ASP. NET in order to build the new mode of engineering calculation. It can fully implement the sharing of the resources and provide the engineering designers a wonderful calculating environment, and the working eifficiency of designers can be enhanced.     

基于B/S结构的数字地质图元数据信息系统设计与实现

以国土资源环境与区域经济信息系统信息共享元数据内容标准草案(“NREDIS”)为依据,结合ASP.NET技术,利用C#语言,设计了一个基于B/S(浏览器/服务器)结构的数字地质图元数据信息系统。实现了元数据标准的浏览和元数据的输入、查询及维护4大功能。研究成果为国家空间信息基础设施和数字地球的建设提供了一定的理论基础和技术原型,推动了地理空间信息的网络发布和共享。     

在水泵制造企业中应用成组技术

通过水泵生产企业现状的调查分析，在为某水泵厂开发计算机辅助企业现代化管理系统的基础上，提出了水泵生产企业运用成组技术，强化企业内部管理的内容和方法。     

基于BIM技术与B/S架构的大坝安全可视化监测系统

为了实现大坝整体结构、安全监测测点布置及监测成果的可视化展示功能,并且能够及时、准确地掌握大坝运行状态和异常情况,以甘再碾压混凝土重力坝为例,对传统大坝安全监测系统存在的问题进行了深入的分析与解答,并围绕问题提出了可视化的大坝安全监测系统思想,利用Revit、Dynamo、Civil3D等主流BIM软件建立了大坝主体结构及监测点的模型族库,集成了大坝及监测系统的三维可视化BIM模型.借用于BIMFACE平台轻量化技术、PHP脚本语言和MySQL数据库等现代化信息技术,开发出基于B/S架构的甘再大坝安全可视化系统,实现了BIM模型的Web轻量化展示,可通过客户端浏览器在三维模型中直观查看大坝结构、监测仪器信息以及监测点时程曲线变化等内容.通过本系统的应用,大大提高了大坝运行期间安全监测的可视化管理水平,同时对传统的大坝安全监测系统提出了现代化的建立方式与思想.     

干旱区B/S模式水库调度系统设计

利用Visual Studio．NET的优良集成开发环境、采用SQL Server 2000作为B／S计算环境数据库服务器的分布式数据管理系统。针对干旱区水库调度的实际特点，选择了适合当地实际特点的预报、调度模型，考虑到该系统维护、升级的需要，系统采用组件技术，对各子系统进行功能分区，模块化处理。系统具备基本信息接收、存储和查询，洪水预报，水位预报，水库调度，成果管理和数据库管理等主要功能。系统界面简洁、友好，功能适用，方便操作。结合实例展示了系统的在干旱区的应用情况以及在进一步推广应用前景。     

灰色动态模型群法在河流水质预测中的应用初探

在对原始数据序列对数变换的基础上，依据灰色系统理论，构造了由6个GM（1，1）模型组成的灰色动态模型群，并用于淮河干流枯水期氨氮浓度变化趋势预测。研究表明，灰色动态模型群法能够充分利用近期水质资料信息预测水质变化趋势；相对单个GM（1，1）模型，灰色动态模型群法能有效改善随机波动数据序列的拟合效果，提高预测精度。     

Mechanism of Fuzilizhong decoction alleviating inflammatory damage of rats with non-alcoholic fatty liver disease

AIM To observe the effect of Fuzilizhong decoction on the inflammatory damage of non-alcoholic fatty liver disease （NAFLD） rats and to explore its mechanism. METHODS SPF male SD rats were randomly divided into 6 groups： control group, model group, high dose （20 mg·kg^-1·d^-1）, middle dose （10 mg·kg^-1·d^-1）, low dose （5 mg·kg^-1·d^-1） Fuzilizhong decoction group and Yishanfu （30 mg·kg^-1·d^-1）group, 8 rats in each group. A NAFLD rat modelwas established by intragastric administration of fat emulsion for 4 weeks. Then the drug was given for 4 weeks in each treatment group. HE staining was performed to observe the histopathological changes of the rat liver.The serum levels of interleukin-2（IL-2）, IL-6 and tumor necrosis factor-α（TNF-α） were measured by ELISA. The expression of toll like receptor 4（TLR4） and NF-κB p65 in liver tissues at mRNA and protein levels was determined by RT-qPCR and Western bolt,respectively. RESULTS Compared with control group, the inflammatory damage of liver tissue was more serious, the serum levels of IL-2, IL-6 and TNF-α, the mRNA expression TLR4 and NF-κB p65 in liver tissues were significantly increased in model group（P<0.05）. However, compared with model group, the liver pathological changes in each treatment group were significantly relieved, the serum levels of IL-2, IL-6 and TNF-α, the mRNA expression of TLR4 and NF-κB p65 in liver tissues were significantly reduced（P<0.05）.In addition, the changes of TLR4 and p-NF-κB p65 protein levels in liver tissue were consistent with the changes of TLR4 and NF-κB p65 mRNA. CONCLUSION Fuzilizhong decoction attenuates the inflammatory damages of NAFLD in rats by inhibiting TLR4/NF-κB p65 signaling pathway.     

Aurasperone A Inhibits SARS CoV-2 In Vitro: An Integrated In Vitro and In Silico Study

Several natural products recovered from a marine-derived Aspergillus niger were tested for their inhibitory activity against SARS CoV-2 in vitro. Aurasperone A (3) was found to inhibit SARS CoV-2 efficiently (IC₅₀ = 12.25 µM) with comparable activity with the positive control remdesivir (IC₅₀ = 10.11 µM). Aurasperone A exerted minimal cytotoxicity on Vero E6 cells (CC₅₀ = 32.36 mM, SI = 2641.5) and it was found to be much safer than remdesivir (CC₅₀ = 415.22 µM, SI = 41.07). To putatively highlight its molecular target, aurasperone A was subjected to molecular docking against several key-viral protein targets followed by a series of molecular dynamics-based in silico experiments that suggested M^pro to be its primary viral protein target. More potent anti-SARS CoV-2 M^pro inhibitors can be developed according to our findings presented in the present investigation.