关于Photoshop插件的SAR图像处理探究

SAR图像处理主要包括相干斑抑制、特征提取等,如果在使用Photoshop插件SAR图像处理图片,将主要精力集中于算法的设计和优化方面,可以尽量减少在用户界面、内存管理和基本的图像操作方面的编程,既可以实现多种图像处理,又容易实现功能的充分扩大与填充,从而在最短的时间内做做多的事。     

Effect of nitrogen and nickel on the stability of an Fe-12Cr-23Mn austenitic steel

The effect of nitrogen and nickel on the austenite stability and the structural changes as a result of cold work of an Fe-12Cr-23Mn alloy steel has been examined by transmission electron microscopy and X-ray analysis. Prestrain was performed either at room temperature or at 200° C. Final strain was carried out at liquid nitrogen temperature. The volume fraction of strain-induced martensite decreased by 40% and 12% due to the addition of 2.43% Ni and 0.11% N, respectively, despite whether prestrain was performed or not. The mechanisms are discussed in terms of the phase, stacking faults, dislocation cells and dislocation tangles induced by prestrain and final strain.     

Stability and work hardening of an Fe-12Cr-23Mn austenitic steel

The effect of pre-strain on the strain-induced martensitic transformation of an Fe-12Cr-23Mn austenitic steel has been investigated through transmission electron microscopy and X-ray analysis. Pre-strain was performed either at room temperature or at 200° C. Final strain was carried out at liquid-nitrogen temperature. The phase was shown to form on {1 1 1} planes of the austenite matrix predominantly by overlapping of stacking faults. The martensite transformation sequence was . Nucleation of the phase mainly occurred at intersections of bands. Austenite stability was shown to increase by pre-strain at 25° C or 200° C. Pre-strain at 200° C has a greater effect on austenite stability than does pre-strain at 25° C. The mechanism was discussed in terms of martensite transformation rate and various substructures introduced during straining. Work hardening was shown to depend on the degree of pre-strain and final strain. The correlation between work hardening and substructures introduced during straining was examined.     

Adhesion to skin

The failure energy of an adhesive bond can be factorized into two terms, one of which is a dimensionless loss function and the other, the true interfacial bonding energy, ₀. Experimental techniques have been developed to effect a separation of these two terms and thus measure ₀, but they are unsuitable for the pressure-sensitive adhesives used in surgical tapes and dressings. This is because these adhesives flow readily under load. This paper describes an extrapolation technique by which this problem can be resolved. Adhesive peel data are extrapolated both to zero peel velocity and zero load, to give a true threshold value for peeling energy which is independent of temperature. Values of ₀ are given for a natural-rubber based adhesive and substrates of glass and human skinin vivo. For glass ₀ = 28J m^–2 and for normal skin ₀ 14J m-2.     

高温钎料PdCu-Ti在氧化铝陶瓷上的润湿性及界面反应

本文采用座滴法试验研究了合金系统ＰｄＣｕ－Ｔｉ在Ａｌ２Ｏ３上润湿性的变化规律，探讨了界面冶金及结合等行为，运用热力学理论对结果进行了分析，随Ｔｉ含量的增加及Ｐｄ含量的减少润湿角逐渐降低，Ｔｉ的加入使界面发生了一个双重变化；液相侧富氧，钛吸收层的生成及随后的固相侧氧化钛的生成，只有界面上生成一氧化钛，才能有较好的润湿行为和较强的结合力。     

Senescence Marker Protein 30 (SMP30): A Novel Pan-Species Diagnostic Marker for the Histopathological Diagnosis of Breast Cancer in Humans and Animals

Senescence marker protein 30 (SMP30) is a cell survival factor playing an important role in vitamin C synthesis and antiapoptosis. Moreover, its cytoprotective role suggests a possibility to be related to cancer cell survival. Mammary carcinoma is a common cancer in both humans and animals. Because of its histopathological diversity, especially in the early stage, histopathological diagnosis may be complicated; therefore, a diagnostic marker is helpful for confirmation. The present study analyzed the expression pattern of SMP30 in mammary carcinoma in humans, dogs, and cats. Immunohistochemistry, immunofluorescence, and western blot analysis were used to investigate SMP30 expression patterns. The expression was specifically observed in neoplastic glandular epithelial cells. The expression increased with the malignancy of glandular epithelial cells with a highly proliferative status. However, SMP30 expression was low in normal mammary gland tissues or well-differentiated adenoma tissues. The patterns were consistently reproduced in canine primary mammary carcinoma cells and MCF-7 and MDA-MB-231 human carcinoma cell lines. This study provides useful information to understand SMP30 expression in various stages of mammary carcinoma and to suggest its utility as a pan-species diagnostic marker, thereby helping to establish strategies for diagnosing mammary carcinoma in several species.     

Evaluation of the Effects of Developmental Trauma on Neurotransmitter Systems Using Functional Molecular Imaging

Early life stress (ELS) is strongly associated with psychiatric disorders such as anxiety, depression, and schizophrenia in adulthood. To date, biological, behavioral, and structural aspects of ELS have been studied extensively, but their functional effects remain unclear. Here, we examined NeuroPET studies of dopaminergic, glutamatergic, and serotonergic systems in ELS animal models. Maternal separation and restraint stress were used to generate single or complex developmental trauma. Body weights of animals exposed to single trauma were similar to those of control animals; however, animals exposed to complex trauma exhibited loss of body weight when compared to controls. In behavioral tests, the complex developmental trauma group exhibited a decrease in time spent in the open arm of the elevated plus-maze and an increase in immobility time in the forced swim test when compared to control animals. In NeuroPET studies, the complex trauma group displayed a reduction in brain uptake values when compared to single trauma and control groups. Of neurotransmitter systems analyzed, the rate of decrease in brain uptake was the highest in the serotonergic group. Collectively, our results indicate that developmental trauma events induce behavioral deficits, including anxiety- and depressive-like phenotypes and dysfunction in neurotransmitter systems.     

Biflavonoid-Induced Disruption of Hydrogen Bonds Leads to Amyloid-β Disaggregation

Deposition of amyloid β (Aβ) fibrils in the brain is a key pathologic hallmark of Alzheimer’s disease. A class of polyphenolic biflavonoids is known to have anti-amyloidogenic effects by inhibiting aggregation of Aβ and promoting disaggregation of Aβ fibrils. In the present study, we further sought to investigate the structural basis of the Aβ disaggregating activity of biflavonoids and their interactions at the atomic level. A thioflavin T (ThT) fluorescence assay revealed that amentoflavone-type biflavonoids promote disaggregation of Aβ fibrils with varying potency due to specific structural differences. The computational analysis herein provides the first atomistic details for the mechanism of Aβ disaggregation by biflavonoids. Molecular docking analysis showed that biflavonoids preferentially bind to the aromatic-rich, partially ordered N-termini of Aβ fibril via the π–π interactions. Moreover, docking scores correlate well with the ThT EC₅₀ values. Molecular dynamic simulations revealed that biflavonoids decrease the content of β-sheet in Aβ fibril in a structure-dependent manner. Hydrogen bond analysis further supported that the substitution of hydroxyl groups capable of hydrogen bond formation at two positions on the biflavonoid scaffold leads to significantly disaggregation of Aβ fibrils. Taken together, our data indicate that biflavonoids promote disaggregation of Aβ fibrils due to their ability to disrupt the fibril structure, suggesting biflavonoids as a lead class of compounds to develop a therapeutic agent for Alzheimer’s disease.