18,840 research outputs found

    Simulations with Complex Measures

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    Towards a solution to the sign problem in the simulations of systems having indefinite or complex-valued measures, we propose a new approach which yields statistical errors smaller than the crude Monte Carlo using absolute values of the original measures. The 1D complex-coupling Ising model is employed as an illustration.Comment: 3 pages, postcript (95K), contribution to LAT93, UM-P-93/10

    Fermionic Field Theory and Gauge Interactions on Random Lattices

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    Random-lattice fermions have been shown to be free of the doubling problem if there are no interactions or interactions of a non-gauge nature. However, gauge interactions impose stringent constraints as expressed by the Ward-Takahashi identities which could revive the free-field suppressed doubler modes in loop diagrams. After introducing a formulation for fermions on a new kind of random lattice, we compare random, naive and Wilson fermions in two dimensional Abelian background gauge theory. We show that the doublers are revived for random lattices in the continuum limit, while demonstrating that gauge invariance plays the critical role in this revival. Some implications of the persistent doubling phenomenon on random lattices are also discussed.Comment: 16 A4 pages, UM-P-93/0

    Research and development in cds photovoltaic film cells final report

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    Fabrication of lightweight, flexible, high efficiency, low cost, thin film, cadmium sulfide solar cells to operate for long periods in space without appreciable degradatio

    Astrometric orbits of SB9 stars

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    Hipparcos Intermediate Astrometric Data (IAD) have been used to derive astrometric orbital elements for spectroscopic binaries from the newly released Ninth Catalogue of Spectroscopic Binary Orbits (SB9). Among the 1374 binaries from SB9 which have an HIP entry, 282 have detectable orbital astrometric motion (at the 5% significance level). Among those, only 70 have astrometric orbital elements that are reliably determined (according to specific statistical tests discussed in the paper), and for the first time for 20 systems, representing a 10% increase relative to the 235 DMSA/O systems already present in the Hipparcos Double and Multiple Systems Annex. The detection of the astrometric orbital motion when the Hipparcos IAD are supplemented by the spectroscopic orbital elements is close to 100% for binaries with only one visible component, provided that the period is in the 50 - 1000 d range and the parallax is larger than 5 mas. This result is an interesting testbed to guide the choice of algorithms and statistical tests to be used in the search for astrometric binaries during the forthcoming ESA Gaia mission. Finally, orbital inclinations provided by the present analysis have been used to derive several astrophysical quantities. For instance, 29 among the 70 systems with reliable astrometric orbital elements involve main sequence stars for which the companion mass could be derived. Some interesting conclusions may be drawn from this new set of stellar masses, like the enigmatic nature of the companion to the Hyades F dwarf HIP 20935. This system has a mass ratio of 0.98 but the companion remains elusive.Comment: Astronomy & Astrophysics, in press (16 pages, 12 figures); also available at http://www.astro.ulb.ac.be/Html/ps.html#Astrometr

    Mixed Quantum/Classical Theory of Rotationally and Vibrationally Inelastic Scattering in Space-fixed and Body-fixed Reference Frames

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    We formulated the mixed quantum/classical theory for rotationally and vibrationally inelastic scattering process in the diatomic molecule + atom system. Two versions of theory are presented, first in the space-fixed and second in the body-fixed reference frame. First version is easy to derive and the resultant equations of motion are transparent, but the state-to-state transition matrix is complex-valued and dense. Such calculations may be computationally demanding for heavier molecules and/or higher temperatures, when the number of accessible channels becomes large. In contrast, the second version of theory requires some tedious derivations and the final equations of motion are rather complicated (not particularly intuitive). However, the state-to-state transitions are driven by real-valued sparse matrixes of much smaller size. Thus, this formulation is the method of choice from the computational point of view, while the space-fixed formulation can serve as a test of the body-fixed equations of motion, and the code. Rigorous numerical tests were carried out for a model system to ensure that all equations, matrixes, and computer codes in both formulations are correct

    Cell surface localization of tissue transglutaminase is dependent on a fibronectin-binding site in its N-terminal beta-sandwich domain

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    Increasing evidence indicates that tissue transglutaminase (tTG) plays a role in the assembly and remodeling of extracellular matrices and promotes cell adhesion. Using an inducible system we have previously shown that tTG associates with the extracellular matrix deposited by stably transfected 3T3 fibroblasts overexpressing the enzyme. We now show by confocal microscopy that tTG colocalizes with pericellular fibronectin in these cells, and by immunogold electron microscopy that the two proteins are found in clusters at the cell surface. Expression vectors encoding the full-length tTG or a N-terminal truncated tTG lacking the proposed fibronectin-binding site (fused to the bacterial reporter enzyme β-galactosidase) were generated to characterize the role of fibronectin in sequestration of tTG in the pericellular matrix. Enzyme-linked immunosorbent assay style procedures using extracts of transiently transfected COS-7 cells and immobilized fibronectin showed that the truncation abolished fibronectin binding. Similarly, the association of tTG with the pericellular matrix of cells in suspension or with the extracellular matrix deposited by cell monolayers was prevented by the truncation. These results demonstrate that tTG binds to the pericellular fibronectin coat of cells via its N-terminal β-sandwich domain and that this interaction is crucial for cell surface association of tTG

    Long-term material compatibility testing system

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    System includes procedure for hermetically sealing solid materials and fluids in glass ampoule and use of temperature-controlled facility containing sample holder, which permits sample containers to be retrieved safely and conveniently. Solid material and fluid are sealed within chemically-clean glass ampoule according to highly detailed procedure

    Novel approach for deriving genome wide SNP analysis data from archived blood spots.

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    RIGHTS : This article is licensed under the BioMed Central licence at http://www.biomedcentral.com/about/license which is similar to the 'Creative Commons Attribution Licence'. In brief you may : copy, distribute, and display the work; make derivative works; or make commercial use of the work - under the following conditions: the original author must be given credit; for any reuse or distribution, it must be made clear to others what the license terms of this work are.BACKGROUND: The ability to transport and store DNA at room temperature in low volumes has the advantage of optimising cost, time and storage space. Blood spots on adapted filter papers are popular for this, with FTA (Flinders Technology Associates) Whatman™TM technology being one of the most recent. Plant material, plasmids, viral particles, bacteria and animal blood have been stored and transported successfully using this technology, however the method of porcine DNA extraction from FTA Whatman™TM cards is a relatively new approach, allowing nucleic acids to be ready for downstream applications such as PCR, whole genome amplification, sequencing and subsequent application to single nucleotide polymorphism microarrays has hitherto been under-explored. FINDINGS: DNA was extracted from FTA Whatman™TM cards (following adaptations of the manufacturer's instructions), whole genome amplified and subsequently analysed to validate the integrity of the DNA for downstream SNP analysis. DNA was successfully extracted from 288/288 samples and amplified by WGA. Allele dropout post WGA, was observed in less than 2% of samples and there was no clear evidence of amplification bias nor contamination. Acceptable call rates on porcine SNP chips were also achieved using DNA extracted and amplified in this way. CONCLUSIONS: DNA extracted from FTA Whatman cards is of a high enough quality and quantity following whole genomic amplification to perform meaningful SNP chip studies
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