计及负荷转移需求响应的低碳数据中心光储容量优化配置

为了解决高耗能数据中心低碳化转型问题,提出一种计及负荷转移需求响应的低碳数据中心光储容量配置方法。根据延时特性将数据中心负载分为交互性负载与延时性负载,通过比特-瓦特变换与数据中心电能使用效率得出负载与数据中心能耗之间的关系,以总净现值成本最低为目标函数,考虑清洁能源高渗透率水平、数据流需求响应管控约束,获得数据中心的光储容量配置结果。算例验证了所提方法的有效性。     

车轴径向锻造过程浅析

以某车轴径向锻造为例,分析锻造加热以及锻造工艺的特点,并且用滑移法分析径向锻造变形过程,建立了外摩擦影响下的滑移场模式,并做出了与之相对应的速端图。     

基于改进边界距离变换的路径提取算法研究*

针对虚拟内窥镜中心路径提取算法时间效率不高的问题,通过改进边界距离变换,提出了中心路径的快速提取算法。首先建立最小距离场,在边界内推过程,仅扫描并处理与边界点面连接的点并对其设标记属性,每次向里剥离一层体素标记属性随之增加,直到对内部点集都置到边界的最小边界距离值（DFB）;然后找到DFB值不小于其所有面邻接点DFB值的体素点,即3D局部最大值;最后用最短路径相连3D局部最大值,形成中心线。实验结果表明,改进的中心路径提取算法的时间效率较传统距离变换算法有很大提高。     

小波变换在毫米波辐射计信号去噪中的应用

本文基于小波理论的基础上介绍小波函数的选取和小波去噪的方法,并结合毫米波辐射计输出信号为例进行具体的分析。     

List partitions

By definition, apartition of a list is a division of that list into nonempty contiguous segments. Many programming and operations research problems can be specified in terms of list partitions, and we present a hierarchy of theorems for deriving programs from such specifications. Throughout, reasoning is conducted in an equational style using the calculus for program synthesis developed by Bird and Meertens.Supported by a BP research studentship.     

基于预测编码与DCT变换编码的比较

深入分析了预测编码与DCT变换编码的异同点，并从编码增益、块效应系数、预测与变换与变换前后的能量关系等多方面比较了两种编码的优缺点。     

高铁赤泥中铝的赋存状态及铝铁分离技术研究

针对拜耳法高铁赤泥无害化处置与资源化利用难题,研究了高铁赤泥中铝的赋存状态及其对铝铁分离的影响。借助XRD、铁化学物相分析、SEM-EDS等检测手段,主要关注高铁赤泥的化学组成、矿物组成以及铝的赋存状态等工艺矿物学特征。赤泥的主要组成矿物为褐铁矿、赤铁矿和铝针铁矿和钛铁矿。查明赤泥中的铁主要以针铁矿、赤铁矿的形式存在;铝主要以类质同象存在于针铁矿中,形成铝针铁矿,部分以三水铝石的形式存在,铁铝共生关系密切。赋存于针铁矿中的铝采用常规物理分选方法无法实现铝铁分离,利用磁化焙烧和悬浮焙烧预还原-电炉熔炼工艺分别尝试对高铁赤泥进行铝铁分离,磁化焙烧能够实现赤铁矿、针铁矿向磁铁矿的定向转化,但不能有效破坏铁矿物中铝的类质同象结构,无法实现铝和铁的分离,导致磁选铁精矿中TFe品位低、Al2O3含量高;悬浮焙烧预还原-电炉熔炼工艺能有效实现高铁赤泥的铁铝分离与综合利用,当原料TFe品位为46.85%、Al2O3含量为13.31%时,可获得TFe 92.86%的炼钢用生铁,同时所得到的矿渣产品可以作为生产铝酸盐水泥熟料的原料。可见,悬浮焙烧预还原-电炉熔炼工艺可以有效破坏矿石内部铝和铁类质同象的晶格结构,实现了铝铁的高效分离,为高铁赤泥的无害化处置与资源化利用提供了新途径。     

冷拔无缝钢管开裂分析

在无缝钢管的冷拔过程中,存在着冷作硬化和氢脆现象,它们是造成钢管开裂的主要原因。此文对两个现象进行了分析,提出了一些防止钢管开裂的措施。     

Generation and Identification of the Number of Copies of Exogenous Genes and the T-DNA Insertion Site in SCN-Resistance Transformation Event ZHs1-2

Soybean cyst nematode (SCN, Heterodera glycines Ichinohe) causes an estimated economic loss of about USD 3 billion each year in soybean (Glycine max L.) production worldwide. Overexpression of resistance genes against SCN provides a powerful approach to develop SCN resistance cultivars in soybean. The clarification of molecular characterization in transformation events is a prerequisite for ecological risk assessment, food safety, and commercial release of genetically modified crops. Here, we generated transgenic events harboring the BCN (beet cyst nematode) resistance Hs1^pro−1 gene using the Agrobacterium-mediated method in soybean, evaluated their resistance to SCN infection, and clarified the molecular characterization of one of the transformation events. Five independent and stable inheritable transformation events were generated by an Agrobacterium-mediated transformation method. SCN resistance tests showed the average number of developed females per plant and female index (FI) in T4 ZHs1-1, ZHs1-2, ZHs1-3, ZHs1-4, and ZHs1-5 transformation events were significantly lower than that in the nontransgenic control. Among these, the ZHs1-2 transformation event had the lowest number of developed females per plant and FI. Southern hybridization showed the exogenous target Hs1^pro−1 gene was inserted in one copy and the Bar gene was inserted two copies in the ZHs1-2 transformation event. The exogenous T-DNA fragment was integrated in the reverse position of Chr02: 5351566–5231578 (mainly the Bar gene expression cassette) and in the forward position of Chr03: 17083358–17083400 (intact T-DNA, including Hs1^pro−1 and Bar gene expression cassette) using a whole genome sequencing method (WGS). The results of WGS method and Southern hybridization were consistent. All the functional elements of exogenous T-DNA fragments were verified by PCR using specific primer pairs in the T5 and T6 ZHs1-2 transformation events. These results demonstrated that the overexpression of Hs1^pro−1 gene enhanced SCN resistance, and provide an important reference for the biosafety assessment and the labeling detection in transformation event ZHs1-2.     

Having a Same Type IIS Enzyme’s Restriction Site on Guide RNA Sequence Does Not Affect Golden Gate (GG) Cloning and Subsequent CRISPR/Cas Mutagenesis

Golden gate/modular cloning facilitates faster and more efficient cloning by utilizing the unique features of the type IIS restriction enzymes. However, it is known that targeted insertion of DNA fragment(s) must not include internal type IIS restriction recognition sites. In the case of cloning CRISPR constructs by using golden gate (GG) cloning, this narrows down the scope of guide RNA (gRNA) picks because the selection of a good gRNA for successful genome editing requires some obligation of fulfillment, and it is unwanted if a good gRNA candidate cannot be picked only because it has an internal type IIS restriction recognition site. In this article, we have shown that the presence of a type IIS restriction recognition site in a gRNA does not affect cloning and subsequent genome editing. After each step of GG reactions, correct insertions of gRNAs were verified by colony color and restriction digestion and were further confirmed by sequencing. Finally, the final vector containing a Cas12a nuclease and four gRNAs was used for Agrobacterium-mediated citrus cell transformation. Sequencing of PCR amplicons flanking gRNA-2 showed a substitution (C to T) mutation in transgenic plants. The knowledge derived from this study could widen the scope of GG cloning, particularly of gRNAs selection for GG-mediated cloning into CRISPR vectors.