Stability of hydrogenated nanodiamonds under extreme ultraviolet irradiation

It is generally accepted that diamond is resistant to a wide spectrum of electromagnetic radiation from the ultraviolet through to the soft X-ray range, which makes it very attractive for the fabrication of diamond-based photodetectors. However the effect of photon radiation on the diamond structure has not yet been examined. In the work presented here, photoelectron spectroscopy has been used to study the graphitization of nanodiamond crystallites exposed to extreme ultraviolet radiation. Under such irradiation, the surface hydrogen groups and graphite species are found to prevent graphitization. The mechanism of radiation-induced nanodiamond graphitization is discussed.     

量化网络风险

基本风险分析技术能帮助您从整个电力行业分布的角度了解工业控制系统和SCADA(数据采集与监控)系统中的网络威胁。这一步骤将帮助您规划一个防御性的策略。2006年8月19号,Brown' s Ferry核电站因为过程控制网络流量过大而堵塞,导致了再循环泵的损坏。操作员按照操作手册要求将其关闭,并将系统调整到安全状态。一份后续的美国核管理委员会(NRC)报告确定其根源为未确定来源的车间计算机网络通信量过大。由此采取了运     

Constructing Facial Identity Surfaces for Recognition

We present a novel approach to face recognition by constructing facial identity structures across views and over time, referred to as identity surfaces, in a Kernel Discriminant Analysis (KDA) feature space. This approach is aimed at addressing three challenging problems in face recognition: modelling faces across multiple views, extracting non-linear discriminatory features, and recognising faces over time. First, a multi-view face model is designed which can be automatically fitted to face images and sequences to extract the normalised facial texture patterns. This model is capable of dealing with faces with large pose variation. Second, KDA is developed to compute the most significant non-linear basis vectors with the intention of maximising the between-class variance and minimising the within-class variance. We applied KDA to the problem of multi-view face recognition, and a significant improvement has been achieved in reliability and accuracy. Third, identity surfaces are constructed in a pose-parameterised discriminatory feature space. Dynamic face recognition is then performed by matching the object trajectory computed from a video input and model trajectories constructed on the identity surfaces. These two types of trajectories encode the spatio-temporal dynamics of moving faces.     

Effect of thiourea and saccharin on the roughness of electrodeposited ultrathin nickel and cobalt layers

Ni and Co films were produced by electrodeposition from plating baths containing either thiourea or saccharin. The effect of the organic additives on surface roughness was studied for the Ni-thiourea, Ni-saccharin, Co-thiourea and Co-saccharin systems. Layer thicknesses were varied from 1 to 10 nm and the additive concentration was varied from about 1 M to 1 mM. Contact mode atomic force microscopy was used to measure both the root mean square (RMS) peak height (nm) and the areal peak density (m^–2) of each film. Although the RMS peak height and areal density were both influenced by film thickness and by additive concentration, the two roughness measures provide complementary information on the layer morphology and growth mechanisms. The four systems studied responded differently to changes in the concentration of the added organic. For example, for films 8 nm thick, addition of 1.22 × 10^–3 thiourea reduced the Ni peak density about 80%; in contrast, the Co peak density was increased over 180% by addition of 1.25 × 10^–3 thiourea. Use of peak height and peak density data to infer growth mechanisms for ultrathin films is discussed.     

Canine neosporosis: clinical signs, diagnosis, treatment and isolation of Neospora caninum in mice and cell culture

Clinical signs, diagnosis, treatment and isolation of Neospora caninum from two littermate dogs are described. Three of six pups from a Labrador bitch developed paralysis. Neosporosis was diagnosed ante mortem by serological examination in two of the affected pups. At necropsy, tissue cysts were seen in unstained smears and in histologic sections of their brains. Tissue cysts were often thin-walled (approximately 1 micron) but antigenically and ultrastructurally identified as N. caninum. Furthermore, N. caninum (isolates NC-4, NC-5) was isolated in mice and in cell cultures inoculated with neural tissues of these two dogs. Serological diagnosis of neosporosis using a variety of tests is discussed.     

Epithelial carcinogenesis in the mouse: correlating the genetics and the biology

Tumour formation relies on a complex combination of genetic and environmental factors. In particular, the contributions from inherited predisposition genes as well as carcinogens, for example from cigarettes or in the diet, are amongst the major contributors to tumorigenesis. Since the study of such processes in particularly difficult in human cancers, the availability of a well-defined model system is of obvious benefit. The mouse skin model of multistage carcinogenesis offers an excellent tool for the study of the target cells, the target genes and the biological events associated with neoplasia. In this system, tumorigenesis occurs in a series of defined stages, each of which is characterized by specific and reproducible alterations in genes such as H-ras, cyclin D1, p53 and p16INK4A. Additional changes occur in the production of, or response to, factors such as transforming growth factor beta (TGF beta). These genetic and biological alterations are mirrored in human tumours of epithelial origin. Hence, research into the general principles of tumour initiation, promotion and progression in the context of the mouse skin model is likely to prove valuable in the continual search for new methods for the diagnosis, prevention, and therapeutic treatment of human cancers.     

Evaluation of intratympanic formulations for inner ear delivery: methodology and sustained release formulation testing

A convenient and efficient in vitro diffusion cell method to evaluate formulations for inner ear delivery via the intratympanic route is currently not available. The existing in vitro diffusion cell systems commonly used to evaluate drug formulations do not resemble the physical dimensions of the middle ear and round window membrane. The objectives of this study were to examine a modified in vitro diffusion cell system of a small diffusion area for studying sustained release formulations in inner ear drug delivery and to identify a formulation for sustained drug delivery to the inner ear. Four formulations and a control were examined in this study using cidofovir as the model drug. Drug release from the formulations in the modified diffusion cell system was slower than that in the conventional diffusion cell system due to the decrease in the diffusion surface area of the modified diffusion cell system. The modified diffusion cell system was able to show different drug release behaviors among the formulations and allowed formulation evaluation better than the conventional diffusion cell system. Among the formulations investigated, poly(lactic-co-glycolic acid)–poly(ethylene glycol)–poly(lactic-co-glycolic acid) triblock copolymer systems provided the longest sustained drug delivery, probably due to their rigid gel structures and/or polymer-to-cidofovir interactions.     

Transforming growth factor beta is essential for spindle cell conversion of mouse skin carcinoma in vivo: implications for tumor invasion

Transforming growth factor beta1 (TGF-beta1) regulates both cell growth and cellular plasticity and is therefore important in the molecular control of both the developmental and neoplastic processes. It has been suggested that TGF-beta1 may be a positive or negative regulator of tumorigenesis. Stimulation of tumorigenesis could be due to its action as an immunosuppressor or as an inducer of angiogenesis, or by its direct action on the cell in promoting cellular plasticity. In the current study, we provide evidence that TGF-beta1 can act directly on keratinocytes in vivo to induce the reversible epithelial-mesenchymal conversion of a malignant metastatic keratinocyte cell line. Two squamous clones from the cell line were shown to undergo a reversible conversion to a fibroblastoid phenotype after culture in 1 ng/ml TGF-beta1. The morphological conversion became apparent at 24 h post-TGF-beta treatment and was complete after another 24 h. The conversion was characterized by a rapid delocalization of E-cadherin within 6-12 h posttreatment, followed by down-regulation of E-cadherin levels by 72 h. These squamous clones spontaneously converted to a fibroblastoid phenotype after s.c. injection in nude mice. Importantly, four of four clones that had been stably transfected with a dominant negative TGF-beta type II receptor were unable to undergo this mesenchymal switch in vivo, despite the fact that all clones stably transfected with neomyocin resistance alone retained their spindle characteristics in vivo. This demonstrates that the epithelial-mesenchymal conversion event is mediated directly via the TGF-beta signaling pathway of the tumor cell per se, and that it is sufficient to significantly enhance tumorigenicity and the malignant and invasive characteristics of the tumor in vivo.