29 research outputs found

    The critical fugacity for surface adsorption of self-avoiding walks on the honeycomb lattice is 1+21+\sqrt{2}

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    In 2010, Duminil-Copin and Smirnov proved a long-standing conjecture of Nienhuis, made in 1982, that the growth constant of self-avoiding walks on the hexagonal (a.k.a. honeycomb) lattice is μ=2+2.\mu=\sqrt{2+\sqrt{2}}. A key identity used in that proof was later generalised by Smirnov so as to apply to a general O(n) loop model with n[2,2]n\in [-2,2] (the case n=0n=0 corresponding to SAWs). We modify this model by restricting to a half-plane and introducing a surface fugacity yy associated with boundary sites (also called surface sites), and obtain a generalisation of Smirnov's identity. The critical value of the surface fugacity was conjectured by Batchelor and Yung in 1995 to be yc=1+2/2n.y_{\rm c}=1+2/\sqrt{2-n}. This value plays a crucial role in our generalized identity, just as the value of growth constant did in Smirnov's identity. For the case n=0n=0, corresponding to \saws\ interacting with a surface, we prove the conjectured value of the critical surface fugacity. A crucial part of the proof involves demonstrating that the generating function of self-avoiding bridges of height TT, taken at its critical point 1/μ1/\mu, tends to 0 as TT increases, as predicted from SLE theory.Comment: Major revision, references updated, 25 pages, 13 figure

    SARS-CoV-2 variants of interest and concern naming scheme conducive for global discourse

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    A group convened and led by the Virus Evolution Working Group of the World Health Organization reports on its deliberations and announces a naming scheme that will enable clear communication about SARS-CoV-2 variants of interest and concern.Molecular basis of virus replication, viral pathogenesis and antiviral strategie

    Geographical and temporal distribution of SARS-CoV-2 clades in the WHO European Region, January to June 2020

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    We show the distribution of SARS-CoV-2 genetic clades over time and between countries and outline potential genomic surveillance objectives. We applied three available genomic nomenclature systems for SARS-CoV-2 to all sequence data from the WHO European Region available during the COVID-19 pandemic until 10 July 2020. We highlight the importance of real-time sequencing and data dissemination in a pandemic situation. We provide a comparison of the nomenclatures and lay a foundation for future European genomic surveillance of SARS-CoV-2.Peer reviewe
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