159 research outputs found

    Two-Dimensional Critical Percolation: The Full Scaling Limit

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    We use SLE(6) paths to construct a process of continuum nonsimple loops in the plane and prove that this process coincides with the full continuum scaling limit of 2D critical site percolation on the triangular lattice -- that is, the scaling limit of the set of all interfaces between different clusters. Some properties of the loop process, including conformal invariance, are also proved.Comment: 45 pages, 12 figures. This is a revised version of math.PR/0504036 without the appendice

    A lower bound for the mass of axisymmetric connected black hole data sets

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    We present a generalisation of the Brill-type proof of positivity of mass for axisymmetric initial data to initial data sets with black hole boundaries. The argument leads to a strictly positive lower bound for the mass of simply connected, connected axisymmetric black hole data sets in terms of the mass of a reference Schwarzschild metric

    Injectivity of sections of convex harmonic mappings and convolution theorems

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    In the article the authors consider the class H0{\mathcal H}_0 of sense-preserving harmonic functions f=h+gf=h+\overline{g} defined in the unit disk z<1|z|<1 and normalized so that h(0)=0=h(0)1h(0)=0=h'(0)-1 and g(0)=0=g(0)g(0)=0=g'(0), where hh and gg are analytic in the unit disk. In the first part of the article we present two classes PH0(α)\mathcal{P}_H^0(\alpha) and GH0(β)\mathcal{G}_H^0(\beta) of functions from H0{\mathcal H}_0 and show that if fPH0(α)f\in \mathcal{P}_H^0(\alpha) and FGH0(β)F\in\mathcal{G}_H^0(\beta), then the harmonic convolution is a univalent and close-to-convex harmonic function in the unit disk provided certain conditions for parameters α\alpha and β\beta are satisfied. In the second part we study the harmonic sections (partial sums) sn,n(f)(z)=sn(h)(z)+sn(g)(z), s_{n, n}(f)(z)=s_n(h)(z)+\overline{s_n(g)(z)}, where f=h+gH0f=h+\overline{g}\in {\mathcal H}_0, sn(h)s_n(h) and sn(g)s_n(g) denote the nn-th partial sums of hh and gg, respectively. We prove, among others, that if f=h+gH0f=h+\overline{g}\in{\mathcal H}_0 is a univalent harmonic convex mapping, then sn,n(f)s_{n, n}(f) is univalent and close-to-convex in the disk z<1/4|z|< 1/4 for n2n\geq 2, and sn,n(f)s_{n, n}(f) is also convex in the disk z<1/4|z|< 1/4 for n2n\geq2 and n3n\neq 3. Moreover, we show that the section s3,3(f)s_{3,3}(f) of fCH0f\in {\mathcal C}_H^0 is not convex in the disk z<1/4|z|<1/4 but is shown to be convex in a smaller disk.Comment: 16 pages, 3 figures; To appear in Czechoslovak Mathematical Journa

    Global Genotype-Phenotype Correlations in Pseudomonas aeruginosa

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    Once the genome sequence of an organism is obtained, attention turns from identifying genes to understanding their function, their organization and control of metabolic pathways and networks that determine its physiology. Recent technical advances in acquiring genome-wide data have led to substantial progress in identifying gene functions. However, we still do not know the function of a large number of genes and, even when a gene product has been assigned to a functional class, we cannot normally predict its contribution to the phenotypic behaviour of the cell or organism - the phenome. In this study, we assessed bacterial growth parameters of 4030 non-redundant PA14 transposon mutants in the pathogenic bacterium Pseudomonas aeruginosa. The genome-wide simultaneous analysis of 119 distinct growth-related phenotypes uncovered a comprehensive phenome and provided evidence that most genotypes are not phenotypically isolated but rather define specific complex phenotypic clusters of genotypes. Since phenotypic overlap was demonstrated to reflect the relatedness of genotypes on a global scale, knowledge of an organism's phenome might significantly contribute to the advancement of functional genomics

    Sensory Input Pathways and Mechanisms in Swallowing: A Review

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    Over the past 20 years, research on the physiology of swallowing has confirmed that the oropharyngeal swallowing process can be modulated, both volitionally and in response to different sensory stimuli. In this review we identify what is known regarding the sensory pathways and mechanisms that are now thought to influence swallowing motor control and evoke its response. By synthesizing the current state of research evidence and knowledge, we identify continuing gaps in our knowledge of these mechanisms and pose questions for future research
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