Fission of solitary wave in stratified fluid

In this paper, we study the fission of a solitary wave in the stratified fluid with a free surface. It has been discovered that there is no difference between the fissions of the internal solitary waves in odd or even modes, and the effect of the stratification on the fission of a surface solitary wave can almost be neglected

GPS变形监测平差计算及不确定度分析

全球定位系统（GPS）是一种全天候、高精度的连续定位系统，它以速度快、方法灵活多样、操作简便等优势被广泛应用于工程测量和变形监测中。结合水厂铁矿GPS边坡变形监测实例，对GPS监测网的星历预报、基线向量平差计算、网平差计算、结果及残差不确定度进行了细致分析研究，以验证GPS技术在边坡变形监测中的可靠性和精度。

MEMS材料力学性能的测试技术

微电子机械系统（MEMS）技术的迅速崛起，推动了所用材料微尺度力学性能测试技术的发展，首先按作用方式将实验分成压痕／划痕、弯曲、拉伸、扭转四大类，系统介绍检测MEMS材料微尺度力学性能的微型试样、测试方法及其实验结果。测试材料主要有硅、氧化硅、氮化硅和一些金属。实验结果主要包括基本的力学性能参数如弹性模量、残余应力、屈服强度、断裂强度和疲劳强度等。最后，简要分析了未来的发展需求。

Comprometimento organizacional afetivo : um estudo na Câmara dos Deputados

Avalia o grau de comprometimento afetivo dos funcionários de alguns setores da Câmara dos Deputados, tendo por base uma pesquisa de campo com aplicação de questionário. Identifica os diferentes padrões de comprometimento, segundo os dados biográficos e funcionais dos servidores, e analisa em que medida o comportamento afetivo prevalece sobre os demais.

低能离子束方法制备Fe组分渐变的Fe-Si薄膜

利用质量分离的低能离子束技术 ,获得了Fe组分渐变的Fe Si薄膜。利用俄歇电子能谱法 (AES)、X射线衍射法 (XRD)以及X射线光电子能谱法 (XPS)测试了薄膜的组分、结构特性。测试结果表明 ,在室温下制备的Fe Si薄膜呈非晶态。非晶薄膜在 40 0℃下退火 2 0min后晶化 ,没有Fe的硅化物相形成。退火后Fe Si薄膜的Fe组分从表面向内部逐渐降低。

同轴送粉激光成形中粉末与激光的相互作用

详细介绍了同轴送粉激光成形过程中,金属粉末与激光束相互作用时间的计算方法。在ANSYS软件平台上,建立了金属粉末穿越激光束过程中粉末温度场的计算模型。系统计算了不同颗粒大小316L不锈钢粉末与不同功率激光束相互作用后的温度。在此基础上,计算了金属粉末与激光束的能量交换及金属粉末落入激光熔池后与激光熔池的能量交换。计算结果表明,在激光束直径为3 mm条件下,316L不锈钢粉末穿过功率大于1000 W的激光束后,所有尺寸金属粉末均被熔化,即金属粉末以液态进入激光熔池。通过金属粉末与激光束及激光熔池的能量交换计算,可知在激光成形中,约有5%的激光能量用于加热和熔化粉末,而大约95%的激光能量用于激光熔池的形成及由于热传导造成的热量损失。

Collecção das Leis do Imperio do Brasil de 1855

Parte 1 - Atos do Poder Legislativo

Capturing protein dynamics with time-resolved luminescence spectroscopy

The presented doctoral research utilizes time-resolved spectroscopy to characterize protein dynamics and folding mechanisms. We resolve millisecond-timescale folding by coupling time-resolved fluorescence energy transfer (trFRET) to a continuous flow microfluidic mixer to obtain intramolecular distance distributions throughout the folding process. We have elucidated the folding mechanisms of two cytochromes---one that exhibits two-state folding (cytochrome cb₅₆₂) and one that has both a kinetic refolding intermediate ensemble and a distinct equilibrium unfolding intermediate (cytochrome c₅₅₂). Our data reveal that the distinct structural features of cytochrome c₅₅₂ contribute to its thermostability.

We have also investigated intrachain contact dynamics in unfolded cytochrome cb₅₆₂ by monitoring electron transfer, which occurs as the heme collides with a ruthenium photosensitizer, covalently bound to residues along the polypeptide. Intrachain diffusion for chemically denatured proteins proceeds on the microsecond timescale with an upper limit of 0.1 microseconds. The power-law dependence (slope = -1.5) of the rate constants on the number of peptide bonds between the heme and Ru complex indicate that cytochrome cb₅₆₂ is minimally frustrated.

In addition, we have explored the pathway dependence of electron tunneling rates between metal sites in proteins. Our research group has converted cytochrome b₅₆₂ to a c-type cytochrome with the porphyrin covalently bound to cysteine sidechains. We have investigated the effects of the changes to the protein structure (i.e., increased rigidity and potential new equatorial tunneling pathways) on the electron transfer rates, measured by transient absorption, in a series of ruthenium photosensitizer-modified proteins.

Study on the effects of three fishing baits on the catch composition of malian traps in Lake Kainji

The studies on the effects of three fishing baits on the catch composition of Malian traps in Lake Kainji were investigated. The traps were set between Monai and Taafa fishing villages in the Southern basin of the lake, baited with their respective treatment and were inspected daily for twelve days. A total of 218 fish were caught, of which the highest (54.59%) was caught by corn bran, while the lowest (11.01%) was caught by stomach content and rice bran caught 34.4%. The fish caught comprised of 15 species belonging to 8 families. There was no significant different (P>0.05) in the catch of the various baits. The weight also followed the same trend as the number of fish caught. However, both baits showed better efficiency for Alestes baremose. Tilapia zilli, S. galilaeus, Oreochromis niloticus, Labeo coubie and Distichodus rostratus than other species caught. There was a wide range between the inimum and maximum size of species caught, which showed the efficiency of the traps in capturing small size, juveniles and the adult of large fish species due to small mesh size (1") net-cover of the trap. Recommendations were made on the use of corn and rice bran as baits enhancing catch efficiency for fishes such as O.niloticus, T. zilli, T. galilaeus and D. rostratus

Pulse temporal cleaner based on nonlinear ellipse rotation by using BK7 glass plate

We report a new pulse cleaning technique to enhance the contrast ratio of intense ultra-short laser pulses. A pulse temporal cleaner based on nonlinear ellipse rotation by using BK7 glass plate is developed, and a contrast ratio improvement of two orders of magnitude for the milli-joule level femtosecond input pulses is demonstrated, the total transmission efficiency of the pulse cleaner is 16.7%.

Characterization and developmental regulation of a gene expressed specifically in the skeletogenic lineage of the sea urchin embryo

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.