993 resultados para 124-769C


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Heavy salted and brightly red coloured slices and cuttings of saithe and Alaska pollock (in German called: Lachsersatz) have a long tradition on the German market and a high consumer acceptability. The food colours E 110 and E 124 are used to produce the typical red colour of these products. An allowable limit of 500 mg/kg has been set for the sum of both colours but data on the actual concentrations are missing. In this study the results of colour measurements of various market samples are presented. Furthermore a study was undertaken to determine possiblechanges in colour concentrations during storage of typical products thereof in an house hold refrigerator.

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Analisa aspectos e circunstâncias que circundam a dinâmica do comportamento parlamentar no âmbito de processos decisórios envolvendo matérias que extinguem privilégios e prerrogativas dos mandatos parlamentares

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《高等断裂力学》系统论述断裂力学的基本概念、理论基础、力学原理、分析方法以及断裂力学的实验测定和工程应用。深入阐明了断裂力学各个重要发展阶段的新颖学术思想和原创性工作,同时融会贯通地介绍了国内学者在作者熟悉的若干领域内的创造性贡献。  《高等断裂力学》共14章。第1章介绍断裂力学的历史背景和发展脉络;第2~5章介绍线弹性断裂力学;第6~8章论述弹塑性断裂力学;第9及第10章分别介绍疲劳裂纹扩展和界面裂纹;第11~14章阐述裂纹体弹性动力学和裂纹动态扩展。  《高等断裂力学》适合从事断裂力学研究和应用的科技工作者及工程师使用和参考,也可供力学专业的高年级本科生和研究生阅读参考.

目录

丛书序
序言
第1章 引论
1.1 历史背景
1.2 工程意义
1.3 脆性破坏特征
1.4 断裂力学起源与发展
参考文献

第2章 线弹性断裂力学
2.1 裂纹尖端弹性应力场
2.2 应力强度因子理论
2.3 裂纹扩展能量原理
2.4 裂纹尖端塑性区
2.5 厚度对KC的影响
2.6 裂纹扩展阻力曲线
参考文献

第3章 应力强度因子分析方法
3.1 Williams级数展开与边界配置法
3.2 复变函数方法
3.3 权函数法
3.4 积分变换法
3.5 奇异积分方程
3.6 有限单元法
参考文献

第4章 平面应变断裂韧性
4.1 标准试样
4.2 试样取向与制备
4.3 测试仪器和有效性分析
4.4 KR曲线测试
参考文献

第5章 复合型裂纹的脆断理论
5.1 复合型裂纹变形特征
5.2 应力参数准则
5.3 分支裂纹应力强度因子
5.4 能量释放率准则
5.5 复合型裂纹脆断试验
5.6 理论与实验比较
5.7 塑性变形对金属材料复合型裂纹脆性断裂的影响
参考文献

第6章 弹塑性断裂力学
6.1 J积分原理
6.2 HRR奇性场
6.3 J积分准则
6.4 J控制扩展
6.5 断裂韧性JIC测试
6.6 Dugdale模型
6.7 带状颈缩区模型
6.8 裂纹张开位移准则
参考文献

第7章 裂纹顶端弹塑性高阶场
7.1 高阶场基本方程
7.2 一阶场和二阶场
7.3 高阶场前5项完整结果
7.4 J-Q双参数方法
7.5 J-k断裂准则
7.6 平面应力裂端弹塑性场
参考文献

第8章 理想弹塑性介质扩展裂纹尖端场
8.1 v=0.5时的裂尖渐近场
8.2 v<0.5时的裂尖场
8.3 理想弹塑性介质Ⅲ型扩展裂纹
8.4 扩展裂纹与J积分
参考文献

第9章 疲劳裂纹扩展
9.1 等幅载荷下裂纹扩展
9.2 影响疲劳裂纹扩展的因素
9.3 裂纹闭合效应
94疲劳裂纹扩展门槛值确定
95等幅载荷下疲劳裂纹寿命预测
96变幅载荷下疲劳寿命预测
97缺口根部的疲劳裂纹
参考文献

第10章 界面裂纹
101弹性界面力学
102界面裂纹弹性断裂力学
10.3 典型的界面断裂问题
10.4 界面断裂试验
参考文献

第11章 弹性动力学基本概念及方法
11.1 动态惯性效应
11.2 线弹性动力学基本方程
11.3 复变解析函数
11.4 Laplace变换
11.5 Wiener-Hopf分解
11.6 动态断裂的能量概念
参考文献

第12章 静止裂纹的弹性动力学基本解
121突加反平面剪切载荷
12.2 突加裂纹面正压力
12.3 突加平面内剪切应力情况
124有限长裂纹面突加载荷情况
12.5 动态载荷裂纹的起始扩展
参考文献

第13章 均匀材料中动态扩展裂纹
13.1 动态裂纹定常扩展
13,2裂纹面上集中剪切力
133黏结区模型
13.4 Broberg问题
13.5 对称扩展剪切裂纹
136时间无关载荷作用下裂纹扩展
13.7 时间相关载荷作用下裂纹扩展
13.8 II型超剪切波扩展裂纹
13.9 裂纹尖端超弹性区对I、II型裂纹速度的影响
参考文献

第14章 双材料界面动态裂纹扩展
14.1 准静态动态裂纹扩展
14.2 双材料界面裂纹含接触区跨音速扩展
14.3 界面裂纹的超音速扩展
参考文献
索引

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The objective of the present study was to determine the most suitable extender and their respective dilution ratios for African catfish sperm for artificial induced breeding and cryopreservation purposes. Three natural extenders were tested i.e. coconut water, sugarcane water and soybean solutions, at three different levels of sperm to extender dilutions of 1:20, 1:30 and 1:40. While Ringer solution was used as a control Diluted sperm were fertilized with ready isolated eggs to assess the fertility and hatching rate at 0, 6 and 12 hour intervals. The results showed that the eggs hatched approximately 19 to 27 hours after fertilization. In general, the fertilization and hatching rates decreased with increasing dilution ratio. With respect to natural extenders, the coconut water showed the highest fertility and hatching rates at 1:20 dilution ratio. Therefore, coconut water at 1:20 dilution ratio was the optimal condition for African catfish spermatozoa among the natural extenders investigated.

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Space-resolved spectra of line-shaped laser-produced magnesium plasmas in the normal direction of the target have been obtained using a pinhole crystal spectrograph. These spectra are treated by a spectrum analyzing code for obtaining the true spectra and fine structures of overlapped lines. The spatial distributions of electron temperature and density along the normal direction of the target surface have been obtained with different spectral diagnostic techniques. Especially, the electron density plateaus beyond the critical surface in line-shaped magnesium plasmas have been obtained with a fitting technique applied to the Stark-broadened Ly-alpha wings of hydrogenic ions. The difference of plasma parameters between those obtained by different diagnostic techniques is discussed. Other phenomena, such as plasma satellites, population inversion, etc., which are observed in magnesium plasmas, are also presented.

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Despite the complexity of biological networks, we find that certain common architectures govern network structures. These architectures impose fundamental constraints on system performance and create tradeoffs that the system must balance in the face of uncertainty in the environment. This means that while a system may be optimized for a specific function through evolution, the optimal achievable state must follow these constraints. One such constraining architecture is autocatalysis, as seen in many biological networks including glycolysis and ribosomal protein synthesis. Using a minimal model, we show that ATP autocatalysis in glycolysis imposes stability and performance constraints and that the experimentally well-studied glycolytic oscillations are in fact a consequence of a tradeoff between error minimization and stability. We also show that additional complexity in the network results in increased robustness. Ribosome synthesis is also autocatalytic where ribosomes must be used to make more ribosomal proteins. When ribosomes have higher protein content, the autocatalysis is increased. We show that this autocatalysis destabilizes the system, slows down response, and also constrains the system’s performance. On a larger scale, transcriptional regulation of whole organisms also follows architectural constraints and this can be seen in the differences between bacterial and yeast transcription networks. We show that the degree distributions of bacterial transcription network follow a power law distribution while the yeast network follows an exponential distribution. We then explored the evolutionary models that have previously been proposed and show that neither the preferential linking model nor the duplication-divergence model of network evolution generates the power-law, hierarchical structure found in bacteria. However, in real biological systems, the generation of new nodes occurs through both duplication and horizontal gene transfers, and we show that a biologically reasonable combination of the two mechanisms generates the desired network.

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The sea urchin embryonic skeleton, or spicule, is deposited by mesenchymal progeny of four precursor cells, the micromeres, which are determined to the skeletogenic pathway by a process known as cytoplasmic localization. A gene encoding one of the major products of the skeletogenic mesenchyme, a prominent 50 kD protein of the spicule matrix, has been characterized in detail. cDNA clones were first isolated by antibody screening of a phage expression library, followed by isolation of homologous genomic clones. The gene, known as SM50, is single copy in the sea urchin genome, is divided into two exons of 213 and 1682 bp, and is expressed only in skeletogenic cells. Transcripts are first detectable at the 120 cell stage, shortly after the segregation of the skeletogenic precursors from the rest of the embryo. The SM50 open reading frame begins within the first exon, is 450 amino acids in length, and contains a loosely repeated 13 amino acid motif rich in acidic residues which accounts for 45% of the protein and which is possibly involved in interaction with the mineral phase of the spicule.

The important cis-acting regions of the SM50 gene necessary for proper regulation of expression were identified by gene transfer experiments. A 562 bp promoter fragment, containing 438 bp of 5' promoter sequence and 124 bp of the SM50 first exon (including the SM50 initiation codon), was both necessary and sufficient to direct high levels of expression of the bacterial chloramphenicol acetyltransferase (CAT) reporter gene specifically in the skeletogenic cells. Removal of promoter sequences between positions -2200 and -438, and of transcribed regions downstream of +124 (including the SM50 intron), had no effect on the spatial or transcriptional activity of the transgenes.

Regulatory proteins that interact with the SM50 promoter were identified by the gel retardation assay, using bulk embryo mesenchyme blastula stage nuclear proteins. Five protein binding sites were identified and mapped to various degrees of resolution. Two sites are homologous, may be enhancer elements, and at least one is required for expression. Two additional sites are also present in the promoter of the aboral ectoderm specific cytoskeletal actin gene CyIIIa; one of these is a CCAA T element, the other a putative repressor element. The fifth site overlaps the binding site of the putative repressor and may function as a positive regulator by interfering with binding of the repressor. All of the proteins are detectable in nuclear extracts prepared from 64 cell stage embryos, a stage just before expression of SM50 is initiated, as well as from blastula and gastrula stage; the putative enhancer binding protein may be maternal as well.

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Two surveys in the German Bight revealed a relatively good recruitment for plaice and cod. However, with the current high effort and uneconomic way of fishing, most of these fish will end as discards. To protect young plaice during the winter months an increase of the mesh opening in beam trawls within the plaice box is suggested. Therefore, the fishermen are called upon to make a more considerated selection of their nets.

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A series of terl-butylperoxide complexes of hafnium, Cp*2Hf(R)(OOCMe3) (Cp* = ((η5-C5Me5); R = Cl, H, CH3, CH2CH3, CH2CH2CH3, CH2CH2CH2CH3, CH2CHMe2, CH=CHCMe3, C6H5, meta-C6H3(CH2)2) and Cp*(η5-C5(CH3)4CH2CH2CH2)Hf(OOCMe3), has been synthesized. One example has been structurally characterized, Cp*2Hf(OOCMe3)CH2CH3 crystallizes in space group P21/c, with a = 19.890(7)Å, b = 8.746(4)Å, c = 17.532(6)Å, β = 124.987(24)°, V = 2498(2)Å3, Z = 4 and RF = 0.054 (2222 reflections, I > 0). Despite the coordinative unsaturation of the hafnium center, the terl-butylperoxide ligand is coordinated in a mono-dentate ligand. The mode of decomposition of these species is highly dependent on the substituent R. For R = H, CH2CH3, CH2CH2CH3, CH2CH2CH2CH3, CH2CHMe2 a clean first order conversion to Cp*2Hf(OCMe3)(OR) is observed (for R CH2CH3, ΔHǂ = 19.6 kcal•mol-1, ΔSǂ = -13 e.u.). These results are discussed in terms of a two step mechanism involving η2-coordination of the terl-butylperoxide ligand. Homolytic O-O bond cleavage is observed upon heating of Cp*2Hf(OOCMe3) R (R = C6H6, meta-C6H3(CH3)2). In the presence of excess 9,10-dihydroanthracene thermolysis of Cp*2Hf(OOCMe3)C6H6 cleanly affords Cp*2Hf(C6H6)OH and HOCMe3 (ΔHǂ = 22.6 kcal•mol-1, ΔSǂ = -9 e.u.). The O-O bond strength in these complexes is thus estimated to be 22 kcal•mol-1.

Cp*2Ta(CH2)H, Cp*2Ta(CHC6H5)H, Cp*2Ta(C6H4)H, Cp*2Ta(CH2=CH2)H and Cp*2Ta(CH2=CHMe)H react, presumably through Cp*2Ta-R intermediates, with H2O to give Cp*2Ta(O)H and alkane. Cp*2Ta(O)H was structurally characterized: space group P21/n, a= 13.073(3)Å, b = 19.337(4)Å, c = 16.002(3)Å, β = 108.66(2)°, V = 3832(1)Å3, Z = 8 and RF = 0.0672 (6730 reflections). Reaction of terlbutylhydroperoxide with these same starting materials ultimately yields Cp*2Ta(O)R and HOCMe3. Cp*2Ta(CH2=CHR)OH species are proposed as intermediates in the olefin hydride reactions. Cp*2Ta(O2)R species can be generated from the reaction of the same starting materials and O2. Lewis acids have been shown to promote oxygen insertion in these complexes.

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The distribution was studied by analysing the catches during four research vessel cruises in summer and eight cruises in winter in the period 1985 - 1993. The emmigration of young saithe, spending the larval and first juvenil stages in the inshore waters of Norway and Scotland, starts during the summer in an age of two years.