Design of a Novel Dual-Band Terahertz Metamaterial Absorber

Plasmonics - We present a novel dual-band terahertz absorber formed by only a patterned U-shaped metallic ring and a metallic ground plane separated by a dielectric layer. Theoretical results show...     

Dynamic-Shift Single- and Double-Negative Refractive Index in a Novel Three-Dimensional Metamaterial

A novel three-dimensional terahertz metamaterial by integrating planar and standup resonators on a sapphire substrate is proposed. This structure shows the capability of dynamic-shifting single- and double-negative refractive index bands under temperature control. When the temperature rises from 160 K to 290 K, the single- and double-negative bands of the metamaterials exhibit blue-shift, which is attributed by the simultaneously tuning of the electromagnetic resonance frequencies of the resonators. If the temperature rises to 300 K, the bianisotropy of the metamaterials increases rapidly, while it performs stable between 160 K and 290 K.

     

Ultrabroadband Mid-infrared Light Absorption Based on a Multi-cavity Plasmonic Metamaterial Array

We present a broadband plasmonic metamaterial absorber in the infrared region based on localized surface plasmon polaritons (LSPPs). The unit cell of the proposed metamaterial absorber consists of a multi-cavity structure, in which absorption resonances can be tuned independently through the modification of the width and shift of metallic walls. In order to avoid the degeneration between two contiguous resonances, which dramatically reduces the bandwidth, we introduce a zigzag design rule to arrange the cavities within a compact unit. Thus, the possible number of resonances is greatly increased, enabling an ultrabroadband absorption. A broadband absorber is demonstrated with only a few-layer structure and it also has an incident-angle-insensitive feature. Our results have potential applications in photovoltaic devices, emitters, sensors, and camouflage systems.     

A Dual-Band Polarization Insensitive Metamaterial Absorber with a Single Square Metallic Patch for Sensing Application

Plasmonics - We proposed a dual-band polarization-insensitive metamaterial absorber consisting of merely the square metallic patch and a continuous metallic ground separated by a middle dielectric...     

A Hybrid Terahertz Metamaterial Sensor Using a Hexagonal Ring Resonator with Bio-medical Applications

Plasmonics - In recent years, novel terahertz (THz) metamaterial sensors are being actively explored by the research community. These structures absorb the incident THz waves, and their absorption...     

A Simple Design of a Multi-Band Terahertz Metamaterial Absorber Based on Periodic Square Metallic Layer with T-Shaped Gap

We present a multi-band terahertz absorber formed by periodic square metallic ribbon with T-shaped gap and a metallic ground plane separated by a dielectric layer. It is demonstrated that absorption spectra of the proposed structure consist of four absorption peaks located at 1.12, 2.49, 3.45, and 3.91 THz with high absorption coefficients of 98.0, 98.9, 98.7, and 99.6%, respectively. It is demonstrated that the proposed absorber has the tunability from single-band to broadband by changing the length of square metallic ribbon and we can also select or tune the frequencies which we want to use by changing polarization angles. Importantly, the quality factor Q at 3.91 THz is 30.1, which is 5.6 times higher than that of 1.12 THz. These results indicate that the proposed absorber has a promising potential for devices, such as detection, sensing, and imaging.

     

Tissue Choline Studied Using a Simple Chemical Assay

Abstract: An enzymatic-radioisotopic assay was used to measure free choline in unextracted tissue. The lowest concentration of free choline in any tissue studied was present in human cerebrospinal fluid (mean, 5.7 μM; range, 1.8–31.2 μM). A postmortem increase in concentration of free choline occurred in blood (O.2 nmol/min ml), kidney (13 nmol/min·g), and liver (22 nmol/min·g) of mice. The concentration of free choline in these tissues was estimated by extrapolation to be 5, 77, and 29 nmol/g (or ml), respectively. Several treatments were found to increase the concentration of free choline. For example, intraperitoneal administration of choline or 2-amino-2-methyl-propanol (a choline oxidase inhibitor) induced an increase in the level of choline in blood, kidneys, liver, and brain of mice, and administration of 2-dimethylaminoethanol (deanol) caused an increase in kidney and liver choline. The level of choline in blood was increased when rats were treated orally with either antibiotics or esters of choline such as phosphorylcholine, glycerylphos-phorylcholine, laroylcholine, or propionylcholine. The results show that the concentration of free choline may be regulated by intestinal metabolism, availability of esterified precursors, and activity of enzymes that metabolize choline.     

Realized evolvability: quantifying phenotypic evolution in a Drosophila clade

Understanding the evolutionary potential of morphological evolution is still a major problem in evolutionary biology. In this study, we tried to quantify the amount of variation of different traits among species of a Drosophila clade reared under standard conditions. Nineteen different traits have been measured on nine species of the same clade, the Neotropical saltans group of Drosophila. Measured traits can be distributed into five categories: size‐traits (wing and thorax), shape indices (ratios among the size traits), number of sternopleural bristles on the thorax, number of abdominal bristles on successive sternites, and dorsal pigmentation of abdomen. All species are of medium size with a generally dark pigmentation. A remarkable feature is the presence of numerous bristles on the 6th sternite of the males, while this segment is bare in other Drosophila species. A multivariate analysis revealed that it was possible to discriminate all the investigated species by using the complete set of measured traits. For each trait, phenotypic variability was investigated at the within‐ and between‐species levels. As a rule, the interspecific coefficient of variation (CV) was much greater than the within species CV, and it is proposed to call it realized evolvability. All possible correlations were calculated between traits across species, providing many unexpected results. Size traits were highly correlated among them, but not correlated with shape indices. Abdominal traits (bristles and pigmentation) were correlated, but often in opposite directions, with thoracic shape indices. Tergite pigmentation was negatively correlated with bristle number on sternite. For the moment, most of the correlations cannot be explained by developmental processes or parallel selective pressures. Nonetheless, mapping the evolution of the two characters on a molecular phylogeny of the studied species revealed two opposite phylogenetic trends for abdominal pigmentation and setation, respectively. Our data suggest a need for similar studies in other well‐defined Drosophila clades.     

Capillary Filling at the Microscale: Control of Fluid Front Using Geometry

We propose an experimental and theoretical framework for the study of capillary filling at the micro-scale. Our methodology enables us to control the fluid flow regime so that we can characterise properties of Newtonian fluids such as their viscosity. In particular, we study a viscous, non-inertial, non-Washburn regime in which the position of the fluid front increases linearly with time for the whole duration of the experiment. The operating shear-rate range of our apparatus extends over nearly two orders of magnitude. Further, we analyse the advancement of a fluid front within a microcapillary in a system of two immiscible Newtonian liquids. We observe a non-Washburn regime in which the front can accelerate or decelerate depending on the viscosity contrast between the two liquids. We then propose a theoretical model which enables us to study and explain both non-Washburn regimes. Furthermore, our theoretical model allows us to put forward ways to control the emergence of these regimes by means of geometrical parameters of the experimental set-up. Our methodology allows us to design and calibrate a micro-viscosimetre which works at constant pressure.     

Mid-infrared study of deoxycytidine at high pressures: evidence of a phase transition

Room temperature mid-infrared experiments between 600 and 1600 cm(-1) have been performed on crystalline deoxycytidine as a function of pressure up to about 10 GPa. The wavenumbers of most vibrational modes shift to higher values with increasing pressures except for a mode near 840 cm(-1). Assignments for the observed modes are made on the basis of work published in the literature. Several anomalies are noted near 4.7 GPa, suggesting a phase transition. Our results for deoxycytidine are compared to similar measurements on cytidine.     

Active Tuning from Narrowband to Broadband Absorbers Using a Sub-wavelength VO2 Embedded Layer

Plasmonics - Metamaterial perfect absorbers (MPAs) with dynamic thermal tuning features are able to control the absorption performance of the resonances, providing diverse applications spanning...     

Development of a Simple Antioxidant Screening Assay Using Human Skin Fibroblasts

The purpose of this study was to develop a simple antioxidant screening assay for quantifying the protective effects of antioxidant enzymes, inhibitors and scavengers against extracellularly generated oxygen species on human skin fibroblast cytotoxicity. Different in vitro oxidative stresses have been studied: xanthine oxidase-hypoxanthine, flavin mononucleotide-NADH, and hydrogen peroxide. Cytotoxicity and protection were evaluated by two procedures: evaluation of the living cells using a colorimetric method (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide MTT), and ability of the viable cells to adherate and proliferate. Hypoxanthine-xanthine oxidase and H^b0₂ induced a dose dependent cytotoxicity only when we considered the delayed toxicity. The influence of the cell density was also investigated. The delayed toxicity was higher when cell density increased. One hundred percent protection against free radical cytotoxicity induced by the three systems were obtained with catalase (500 U/ml). When the oxidative stress used was H₂0₂ 90-96% protection was obtained with deferoxamine an iron chelating agent that prevents iron catalysed radical reactions. Using the colorimetric method no significant protection was obtained when SOD was added before and during the stresses. Using the fibroblasts ability to proliferate SOD (10-150 μ/ml) reduced xanthine oxidase (20 U/1)-hypoxanthine (0.10-0.30mM) or H₂0₂ (1-6mM) cytotoxicity by 15-20%. SOD did not act as antioxidant when the applied stress was mediated by flavin. In this study we showed a paradoxical effect and the cytotoxicity of flavin-NADH system increased when we added SOD to the cell medium. This simple and reliable antioxidant screening assay required no costly or radioactive equipment.     

Parameters Estimation in a Simple Linear Regression Using Rank Set Sampling

Ranked set sampling (RSS) as suggested by MCINTYRE (1952) and TAKAHASI and WAKIMOTO (1968) may be used to estimate the parameters of the simple regression line. The objective is to use the RSS method to increase the efficiency of the estimators relative to the simple random sampling (SRS) method. Estimators of the slope and intercept are considered. Computer simulated results are given, and an example using real data presented to illustrate the computations.     

Rapid and Simple Quantification of Bacterial Cells by Using a Microfluidic Device

This study investigated a microfluidic chip-based system (on-chip flow cytometry) for quantification of bacteria both in culture and in environmental samples. Bacterial numbers determined by this technique were similar to those obtained by direct microscopic count. The time required for this on-chip flow cytometry was only 30 min per 6 samples.     

Simple Purification of a Foreign Protein Using Polyhedrin Fusion in a Baculovirus Expression System

Previously, we found that expression by translational fusion of the polyhedrin (Polh)-green fluorescence protein (GFP) led to the formation of granular structures, and that these fluorescent granules were easily precipitated by high-speed centrifugation. Here, we developed an easy, fast, mass purification system using this baculovirus expression system (BES). An enhanced GFP (EGFP) fused with the Polh gene at the N-terminus, including a linker and enterokinase (EK) site between Polh and EGFP, was expressed in Sf9 cells. The cells infected by AcPolhEKA-EGFP produced fluorescent granules. The EGFP fusion protein was purified from granule-containing cells in three steps: cell harvest, sonication, and EK digestion. Through final enterokinase digestion, EGFP presented mainly in the supernatant, and this supernatant fraction also showed a pure EGFP band. These results suggest that a combined procedure of Polh fusion expression and enterokinase digestion can be used for rapid and easy purification of other proteins.     

Offspring from Mouse Embryos Developed Using a Simple Incubator-Free Culture System with a Deoxidizing Agent

To culture preimplantation embryos in vitro, water-jacketed CO₂ incubators are used widely for maintaining an optimal culture environment in terms of gas phase, temperature and humidity. We investigated the possibility of mouse embryo culture in a plastic bag kept at 37°C. Zygotes derived from in vitro fertilization or collected from naturally mated B6D2F1 female mice were put in a drop of medium on a plastic culture dish and then placed in a commercially available plastic bag. When these were placed in an oven under air at 37°C for 96 h, the rate of blastocyst development and the cell numbers of embryos decreased. However, when the concentration of O₂ was reduced to 5% using a deoxidizing agent and a small oxygen meter, most zygotes developed into blastocysts. These blastocysts were judged normal according to their cell number, Oct3/4 and Cdx2 gene expression levels, the apoptosis rate and the potential for full-term development after embryo transfer to pseudopregnant recipients. Furthermore, using this system, normal offspring were obtained simply by keeping the bag on a warming plate. This culture method was applied successfully to both hybrid and inbred strains. In addition, because the developing embryos could be observed through the transparent wall of the bag, it was possible to capture time-lapse images of live embryos until the blastocyst stage without needing an expensive microscope-based incubation chamber. These results suggest that mouse zygotes are more resilient to their environment than generally believed. This method might prove useful in economical culture systems or for the international shipment of embryos.     

Probing the Architecture of a Simple Kinetochore Using DNA–Protein Crosslinking

In budding yeast, accurate chromosome segregation requires that one and only one kinetochore assemble per chromosome. In this paper, we report the use of DNA–protein crosslinking and nondenaturing gel analysis to study the structure of CBF3, a four-protein complex that binds to the essential CDEIII region of Saccharomyces cerevisiae centromeres. We find that three subunits of CBF3 are in direct contact with CDEIII over a region of DNA that spans 80 bp. A highly asymmetric core complex containing p58^CTF13 p64^CEP3 and p110^NDC10 in direct contact with DNA forms at the genetically defined center of CDEIII. This core complex spans ~56 bp of CEN3. An extended complex comprising the core complex and additional DNA-bound p110^NDC10 also forms. It spans ~80 bp of DNA. CBF3 makes sequence-specific and -nonspecific contacts with DNA. Both contribute significantly to the energy of CBF3–DNA interaction. Moreover, important sequence-specific contacts are made with bases that are not conserved among yeast centromeres. These findings provide a foundation for understanding the organization of the CBF3–centromere complex, a structure that appears to initiate the formation of microtubule attachment sites at yeast kinetochores. These results also have implications for understanding centromere-binding proteins in higher cells.