Experimental Setup for the Measurement of the Thermoelectric Power in Zero and Applied Magnetic Field

An experimental setup was developed for the measurement of the thermoelectric power (TEP, Seebeck coefficient) in the temperature range from 2 to 350 K and magnetic fields up to 140 kOe. The system was built to fit in a commercial cryostat and is versatile, accurate and automated; using two heaters and two thermometers increases the accuracy of the TEP measurement. High density data of temperature sweeps from 2 to 350 K can be acquired in under 16 hours and high density data of isothermal field sweeps from 0 to 140 kOe can be obtained in under 2 hours. Calibrations for the system have been performed on a platinum wire and Bi$_{2}$Sr$_{2}$CaCu$_{2}$O$_{8+\delta}$ high $T_{c}$ superconductors. The measured TEP of phosphor-bronze (voltage lead wire) turns to be very small, where the absolute TEP value of phosphor-bronze wire is much less than 0.5 $\mu$V/K below 80 K. For copper and platinum wires measured against to the phosphor-bronze wire, the agreement between measured results and the literature data is good. To demonstrate the applied magnetic field response of the system, we report measurements of the TEP on single crystal samples of LaAgSb$_{2}$ and CeAgSb$_{2}$ in fields up to 140 kOe.Comment: 10 pages, 8 figures. accepted in Measurement Science and Technolog

Will the U.S. productivity resurgence continue?

U.S. productivity growth has accelerated in recent years, despite a series of negative economic shocks. An analysis of the sources of this growth over the 1995-2003 period suggests that the production and use of information technology account for a large share of the gains. The authors project that during the next decade, private sector productivity growth will continue at a rate of 2.6 percent per year, a significant increase from their 2002 projection of 2.2 percent growth.Productivity ; Information technology

Projecting productivity growth: lessons from the U.S. growth resurgence

Following the 1995-2000 period of more rapid output growth and lower inflation in the United States, economists have strenuously debated whether improvements in economic performance can be sustained. The recession that began in March 2001 intensified the debate, and the economic impacts of the events of September 11 have yet to be fully understood. Both factors add to the considerable uncertainties about future growth that currently face decision makers in both the public and private sectors. ; In this article, the authors analyze the sources of U.S. labor productivity growth in the post-1995 period and present projections for both output and labor productivity growth for the next decade. Despite the 2001 downward revisions to U.S. gross domestic product and software investment, the authors show that information technology (IT) played a substantial role in the U.S. productivity revival. The article then outlines a methodology for projecting trend output and productivity growth. The base-case projection puts the rate of trend productivity growth at 2.21 percent per year over the next decade with a range of 1.33 to 2.92 percent, reflecting fundamental uncertainties about the rate of technological progress in IT-production and investment patterns. The central projection is only slightly below the average growth rate of 2.36 percent during the 1995-2000 period.Productivity ; Technology ; Economic development

Fabrication of three-dimensional suspended, interlayered and hierarchical nanostructures by accuracy-improved electron beam lithography overlay

Nanofabrication techniques are essential for exploring nanoscience and many closely related research fields such as materials, electronics, optics and photonics. Recently, three-dimensional (3D) nanofabrication techniques have been actively investigated through many different ways, however, it is still challenging to make elaborate and complex 3D nanostructures that many researchers want to realize for further interesting physics studies and device applications. Electron beam lithography, one of the two-dimensional (2D) nanofabrication techniques, is also feasible to realize elaborate 3D nanostructures by stacking each 2D nanostructures. However, alignment errors among the individual 2D nanostructures have been difficult to control due to some practical issues. In this work, we introduce a straightforward approach to drastically increase the overlay accuracy of sub-20 nm based on carefully designed alignmarks and calibrators. Three different types of 3D nanostructures whose designs are motivated from metamaterials and plasmonic structures have been demonstrated to verify the feasibility of the method, and the desired result has been achieved. We believe our work can provide a useful approach for building more advanced and complex 3D nanostructures.114sciescopu

Surfactant protein D contributes to ocular defense against Pseudomonas aeruginosa in a murine model of dry eye disease.

Dry eye disease can cause ocular surface inflammation that disrupts the corneal epithelial barrier. While dry eye patients are known to have an increased risk of corneal infection, it is not known whether there is a direct causal relationship between these two conditions. Here, we tested the hypothesis that experimentally-induced dry eye (EDE) increases susceptibility to corneal infection using a mouse model. In doing so, we also examined the role of surfactant protein D (SP-D), which we have previously shown is involved in corneal defense against infection. Scopolamine injections and fan-driven air were used to cause EDE in C57BL/6 or Black Swiss mice (wild-type and SP-D gene-knockout). Controls received PBS injections and were housed normally. After 5 or 10 days, otherwise uninjured corneas were inoculated with 10(9) cfu of Pseudomonas aeruginosa strain PAO1. Anesthesia was maintained for 3 h post-inoculation. Viable bacteria were quantified in ocular surface washes and corneal homogenates 6 h post-inoculation. SP-D was measured by Western immunoblot, and corneal pathology assessed from 6 h to 4 days. EDE mice showed reduced tear volumes after 5 and 10 days (each by ∼75%, p<0.001) and showed fluorescein staining (i.e. epithelial disruption). Surprisingly, there was no significant difference in corneal pathology between EDE mice and controls (∼10-14% incidence). Before bacterial inoculation, EDE mice showed elevated SP-D in ocular washes. After inoculation, fewer bacteria were recovered from ocular washes of EDE mice (<2% of controls, p = 0.0004). Furthermore, SP-D knockout mice showed a significant increase in P. aeruginosa corneal colonization under EDE conditions. Taken together, these data suggest that SP-D contributes to corneal defense against P. aeruginosa colonization and infection in EDE despite the loss of barrier function to fluorescein

Two-Dimensional Nature of Four-Layer Superconductors by Inequivalent Hole Distribution

The magnetization of the four-layer superconductor CuBa_{2}Ca_{3}Cu_4O_{12-\delta} with T_c\simeq117 K is presented. The high-field magnetization around T_c(H) follows the exact two-dimensional scaling function given by Te\v{s}anovi\'{c} and Andreev. This feature is contrary to the inference that the interlayer coupling becomes strong if the number of CuO_2 planes in a unit cell increases. Also, the fluctuation-induced susceptibility in the low-field region was analyzed by using the modified Lawrence-Doniach model. The effective number of independently fluctuating CuO_2 layers per unit cell, g_{\rm eff}, turned out to be \simeq 2 rather than 4, which indicated that two among the four CuO_2 layers were in states far from their optimal doping levels. This result could explain why CuBa_{2}Ca_{3}Cu_4O_{12-\delta} shows two-dimensional behavior.Comment: 5 pages and 4 figure

MicroRNA-762 is upregulated in human corneal epithelial cells in response to tear fluid and Pseudomonas aeruginosa antigens and negatively regulates the expression of host defense genes encoding RNase7 and ST2.

Mucosal surfaces regulate defenses against infection and excessive inflammation. We previously showed that human tears upregulated epithelial expression of genes encoding RNase7 and ST2, which inhibited Pseudomonas aeruginosa invasion of human corneal epithelial cells. Here, microRNA microarrays were used to show that a combination of tear fluid exposure (16 h) then P. aeruginosa antigens (3 h) upregulated miR-762 and miR-1207, and down-regulated miR-92 and let-7b (all > 2-fold) in human corneal epithelial cells compared to P. aeruginosa antigens alone. RT-PCR confirmed miR-762 upregulation ∼ 3-fold in tear-antigen exposed cells. Without tears or antigens, an antagomir reduced miR-762 expression relative to scrambled controls by ∼50%, increased expression of genes encoding RNase7 (∼80 %), ST2 (∼58%) and Rab5a (∼75%), without affecting P. aeruginosa internalization. However, P. aeruginosa invasion was increased > 3-fold by a miR-762 mimic which reduced RNase7 and ST2 gene expression. Tear fluid alone also induced miR-762 expression ∼ 4-fold, which was reduced by the miR-762 antagomir. Combination of tear fluid and miR-762 antagomir increased RNase7 and ST2 gene expression. These data show that mucosal fluids, such as tears, can modulate epithelial microRNA expression to regulate innate defense genes, and that miR-762 negatively regulates RNase7, ST2 and Rab5a genes. Since RNase7 and ST2 inhibit P. aeruginosa internalization, and are upregulated by tear fluid, other tear-induced mechanisms must counteract inhibitory effects of miR-762 to regulate resistance to bacteria. These data also suggest a complex relationship between tear induction of miR-762, its modulation of innate defense genes, and P. aeruginosa internalization

3D quantitative imaging of unprocessed live tissue reveals epithelial defense against bacterial adhesion and subsequent traversal requires MyD88.

While a plethora of in vivo models exist for studying infectious disease and its resolution, few enable factors involved in the maintenance of health to be studied in situ. This is due in part to a paucity of tools for studying subtleties of bacterial-host interactions at a cellular level within live organs or tissues, requiring investigators to rely on overt outcomes (e.g. pathology) in their research. Here, a suite of imaging technologies were combined to enable 3D and temporal subcellular localization and quantification of bacterial distribution within the murine cornea without the need for tissue processing or dissection. These methods were then used to demonstrate the importance of MyD88, a central adaptor protein for Toll-Like Receptor (TLR) mediated signaling, in protecting a multilayered epithelium against both adhesion and traversal by the opportunistic bacterial pathogen Pseudomonas aeruginosa ex vivo and in vivo

Implementation of three-qubit Toffoli gate in a single step

Single-step implementations of multi-qubit gates are generally believed to provide a simpler design, a faster operation, and a lower decoherence. For coupled three qubits interacting with a photon field, a realizable scheme for a single-step Toffoli gate is investigated. We find that the three qubit system can be described by four effective modified Jaynes-Cummings models in the states of two control qubits. Within the rotating wave approximation, the modified Jaynes-Cummings models are shown to be reduced to the conventional Jaynes-Cummings models with renormalized couplings between qubits and photon fields. A single-step Toffoli gate is shown to be realizable with tuning the four characteristic oscillation periods that satisfy a commensurate condition. Possible values of system parameters are estimated for single-step Toffli gate. From numerical calculation, further, our single-step Toffoli gate operation errors are discussed due to imperfections in system parameters, which shows that a Toffoli gate with high fidelity can be obtained by adjusting pairs of the photon-qubit and the qubit-qubit coupling strengthes. In addition, a decoherence effect on the Toffoli gate operation is discussed due to a thermal reservoir.Comment: 8 pages, 4 figures, to appear in PR