67 research outputs found

    Noncommutative gravity: fuzzy sphere and others

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    Gravity on noncommutative analogues of compact spaces can give a finite mode truncation of ordinary commutative gravity. We obtain the actions for gravity on the noncommutative two-sphere and on the noncommutative CP2{\bf CP}^2 in terms of finite dimensional (N×N)(N\times N)-matrices. The commutative large NN limit is also discussed.Comment: LaTeX, 13 pages, section on CP^2 added + minor change

    Teleparallel Gravity and Dimensional Reductions of Noncommutative Gauge Theory

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    We study dimensional reductions of noncommutative electrodynamics on flat space which lead to gauge theories of gravitation. For a general class of such reductions, we show that the noncommutative gauge fields naturally yield a Weitzenbock geometry on spacetime and that the induced diffeomorphism invariant field theory can be made equivalent to a teleparallel formulation of gravity which macroscopically describes general relativity. The Planck length is determined in this setting by the Yang-Mills coupling constant and the noncommutativity scale. The effective field theory can also contain higher-curvature and non-local terms which are characteristic of string theory. Some applications to D-brane dynamics and generalizations to include the coupling of ordinary Yang-Mills theory to gravity are also described.Comment: 31 pages LaTeX; References adde

    Critical Exponents, Hyperscaling and Universal Amplitude Ratios for Two- and Three-Dimensional Self-Avoiding Walks

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    We make a high-precision Monte Carlo study of two- and three-dimensional self-avoiding walks (SAWs) of length up to 80000 steps, using the pivot algorithm and the Karp-Luby algorithm. We study the critical exponents ν\nu and 2Δ4γ2\Delta_4 -\gamma as well as several universal amplitude ratios; in particular, we make an extremely sensitive test of the hyperscaling relation dν=2Δ4γd\nu = 2\Delta_4 -\gamma. In two dimensions, we confirm the predicted exponent ν=3/4\nu = 3/4 and the hyperscaling relation; we estimate the universal ratios  / =0.14026±0.00007\ / \ = 0.14026 \pm 0.00007,  / =0.43961±0.00034\ / \ = 0.43961 \pm 0.00034 and Ψ=0.66296±0.00043\Psi^* = 0.66296 \pm 0.00043 (68\% confidence limits). In three dimensions, we estimate ν=0.5877±0.0006\nu = 0.5877 \pm 0.0006 with a correction-to-scaling exponent Δ1=0.56±0.03\Delta_1 = 0.56 \pm 0.03 (subjective 68\% confidence limits). This value for ν\nu agrees excellently with the field-theoretic renormalization-group prediction, but there is some discrepancy for Δ1\Delta_1. Earlier Monte Carlo estimates of ν\nu, which were  ⁣0.592\approx\! 0.592, are now seen to be biased by corrections to scaling. We estimate the universal ratios  / =0.1599±0.0002\ / \ = 0.1599 \pm 0.0002 and Ψ=0.2471±0.0003\Psi^* = 0.2471 \pm 0.0003; since Ψ>0\Psi^* > 0, hyperscaling holds. The approach to Ψ\Psi^* is from above, contrary to the prediction of the two-parameter renormalization-group theory. We critically reexamine this theory, and explain where the error lies.Comment: 87 pages including 12 figures, 1029558 bytes Postscript (NYU-TH-94/09/01

    Buildout and integration of an automated high-throughput CLIA laboratory for SARS-CoV-2 testing on a large urban campus

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    In 2019, the first cases of SARS-CoV-2 were detected in Wuhan, China, and by early 2020 the first cases were identified in the United States. SARS-CoV-2 infections increased in the US causing many states to implement stay-at-home orders and additional safety precautions to mitigate potential outbreaks. As policies changed throughout the pandemic and restrictions lifted, there was an increase in demand for COVID-19 testing which was costly, difficult to obtain, or had long turn-around times. Some academic institutions, including Boston University (BU), created an on-campus COVID-19 screening protocol as part of a plan for the safe return of students, faculty, and staff to campus with the option for in-person classes. At BU, we put together an automated high-throughput clinical testing laboratory with the capacity to run 45,000 individual tests weekly by Fall of 2020, with a purpose-built clinical testing laboratory, a multiplexed reverse transcription PCR (RT-qPCR) test, robotic instrumentation, and trained staff. There were many challenges including supply chain issues for personal protective equipment and testing materials in addition to equipment that were in high demand. The BU Clinical Testing Laboratory (CTL) was operational at the start of Fall 2020 and performed over 1 million SARS-CoV-2 PCR tests during the 2020-2021 academic year.Boston UniversityPublished versio

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