135 research outputs found

    Tunneling in Fractional Quantum Mechanics

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    We study the tunneling through delta and double delta potentials in fractional quantum mechanics. After solving the fractional Schr\"odinger equation for these potentials, we calculate the corresponding reflection and transmission coefficients. These coefficients have a very interesting behaviour. In particular, we can have zero energy tunneling when the order of the Riesz fractional derivative is different from 2. For both potentials, the zero energy limit of the transmission coefficient is given by T0=cos2π/α\mathcal{T}_0 = \cos^2{\pi/\alpha}, where α\alpha is the order of the derivative (1<α21 < \alpha \leq 2).Comment: 21 pages, 3 figures. Revised version; accepted for publication in Journal of Physics A: Mathematical and Theoretica

    Are critical finite-size scaling functions calculable from knowledge of an appropriate critical exponent?

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    Critical finite-size scaling functions for the order parameter distribution of the two and three dimensional Ising model are investigated. Within a recently introduced classification theory of phase transitions, the universal part of the critical finite-size scaling functions has been derived by employing a scaling limit that differs from the traditional finite-size scaling limit. In this paper the analytical predictions are compared with Monte Carlo simulations. We find good agreement between the analytical expression and the simulation results. The agreement is consistent with the possibility that the functional form of the critical finite-size scaling function for the order parameter distribution is determined uniquely by only a few universal parameters, most notably the equation of state exponent.Comment: 11 pages postscript, plus 2 separate postscript figures, all as uuencoded gzipped tar file. To appear in J. Phys. A

    Annotated bibliography of research in the teaching of English

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    The committee reviews important research works in the teaching of English that have been published in the last year. Committee members include Richard Beach, Martha Bigelow, Martine Braaksma, Deborah Dillon, Jessie Dockter, Lee Galda, Lori Helman, Tanja Janssen, Karen Jorgensen, Richa Kapoor, Lauren Liang, Bic Ngo, David O’Brien, Mistilina Sato, and Cassie Scharber

    Beyond series expansions: mathematical structures for the susceptibility of the square lattice Ising model

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    We first study the properties of the Fuchsian ordinary differential equations for the three and four-particle contributions χ(3) \chi^{(3)} and χ(4) \chi^{(4)} of the square lattice Ising model susceptibility. An analysis of some mathematical properties of these Fuchsian differential equations is sketched. For instance, we study the factorization properties of the corresponding linear differential operators, and consider the singularities of the three and four-particle contributions χ(3) \chi^{(3)} and χ(4) \chi^{(4)}, versus the singularities of the associated Fuchsian ordinary differential equations, which actually exhibit new ``Landau-like'' singularities. We sketch the analysis of the corresponding differential Galois groups. In particular we provide a simple, but efficient, method to calculate the so-called ``connection matrices'' (between two neighboring singularities) and deduce the singular behaviors of χ(3) \chi^{(3)} and χ(4) \chi^{(4)}. We provide a set of comments and speculations on the Fuchsian ordinary differential equations associated with the n n-particle contributions χ(n) \chi^{(n)} and address the problem of the apparent discrepancy between such a holonomic approach and some scaling results deduced from a Painlev\'e oriented approach.Comment: 21 pages Proceedings of the Counting Complexity conferenc

    An inventory of the Aspergillus niger secretome by combining in silico predictions with shotgun proteomics data

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    <p>Abstract</p> <p>Background</p> <p>The ecological niche occupied by a fungal species, its pathogenicity and its usefulness as a microbial cell factory to a large degree depends on its secretome. Protein secretion usually requires the presence of a N-terminal signal peptide (SP) and by scanning for this feature using available highly accurate SP-prediction tools, the fraction of potentially secreted proteins can be directly predicted. However, prediction of a SP does not guarantee that the protein is actually secreted and current <it>in silico </it>prediction methods suffer from gene-model errors introduced during genome annotation.</p> <p>Results</p> <p>A majority rule based classifier that also evaluates signal peptide predictions from the best homologs of three neighbouring <it>Aspergillus </it>species was developed to create an improved list of potential signal peptide containing proteins encoded by the <it>Aspergillus niger </it>genome. As a complement to these <it>in silico </it>predictions, the secretome associated with growth and upon carbon source depletion was determined using a shotgun proteomics approach. Overall, some 200 proteins with a predicted signal peptide were identified to be secreted proteins. Concordant changes in the secretome state were observed as a response to changes in growth/culture conditions. Additionally, two proteins secreted via a non-classical route operating in <it>A. niger </it>were identified.</p> <p>Conclusions</p> <p>We were able to improve the <it>in silico </it>inventory of <it>A. niger </it>secretory proteins by combining different gene-model predictions from neighbouring Aspergilli and thereby avoiding prediction conflicts associated with inaccurate gene-models. The expected accuracy of signal peptide prediction for proteins that lack homologous sequences in the proteomes of related species is 85%. An experimental validation of the predicted proteome confirmed <it>in silico </it>predictions.</p
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