47 research outputs found

    Asymptotic Behavior of Inflated Lattice Polygons

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    We study the inflated phase of two dimensional lattice polygons with fixed perimeter NN and variable area, associating a weight exp⁥[pA−Jb]\exp[pA - Jb ] to a polygon with area AA and bb bends. For convex and column-convex polygons, we show that /Amax=1−K(J)/p~2+O(ρ−p~)/A_{max} = 1 - K(J)/\tilde{p}^2 + \mathcal{O}(\rho^{-\tilde{p}}), where p~=pN≫1\tilde{p}=pN \gg 1, and ρ<1\rho<1. The constant K(J)K(J) is found to be the same for both types of polygons. We argue that self-avoiding polygons should exhibit the same asymptotic behavior. For self-avoiding polygons, our predictions are in good agreement with exact enumeration data for J=0 and Monte Carlo simulations for J≠0J \neq 0. We also study polygons where self-intersections are allowed, verifying numerically that the asymptotic behavior described above continues to hold.Comment: 7 page

    Asymptotic behaviour of convex and column-convex lattice polygons with fixed area and varying perimeter

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    We study the inflated phase of two dimensional lattice polygons, both convex and column-convex, with fixed area A and variable perimeter, when a weight \mu^t \exp[- Jb] is associated to a polygon with perimeter t and b bends. The mean perimeter is calculated as a function of the fugacity \mu and the bending rigidity J. In the limit \mu -> 0, the mean perimeter has the asymptotic behaviour \avg{t}/4 \sqrt{A} \simeq 1 - K(J)/(\ln \mu)^2 + O (\mu/ \ln \mu) . The constant K(J) is found to be the same for both types of polygons, suggesting that self-avoiding polygons should also exhibit the same asymptotic behaviour.Comment: 10 pages, 3 figure

    Integrability as a consequence of discrete holomorphicity: the Z_N model

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    It has recently been established that imposing the condition of discrete holomorphicity on a lattice parafermionic observable leads to the critical Boltzmann weights in a number of lattice models. Remarkably, the solutions of these linear equations also solve the Yang-Baxter equations. We extend this analysis for the Z_N model by explicitly considering the condition of discrete holomorphicity on two and three adjacent rhombi. For two rhombi this leads to a quadratic equation in the Boltzmann weights and for three rhombi a cubic equation. The two-rhombus equation implies the inversion relations. The star-triangle relation follows from the three-rhombus equation. We also show that these weights are self-dual as a consequence of discrete holomorphicity.Comment: 11 pages, 7 figures, some clarifications and a reference adde

    On directed interacting animals and directed percolation

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    We study the phase diagram of fully directed lattice animals with nearest-neighbour interactions on the square lattice. This model comprises several interesting ensembles (directed site and bond trees, bond animals, strongly embeddable animals) as special cases and its collapse transition is equivalent to a directed bond percolation threshold. Precise estimates for the animal size exponents in the different phases and for the critical fugacities of these special ensembles are obtained from a phenomenological renormalization group analysis of the correlation lengths for strips of width up to n=17. The crossover region in the vicinity of the collapse transition is analyzed in detail and the crossover exponent ϕ\phi is determined directly from the singular part of the free energy. We show using scaling arguments and an exact relation due to Dhar that ϕ\phi is equal to the Fisher exponent σ\sigma governing the size distribution of large directed percolation clusters.Comment: 23 pages, 3 figures; J. Phys. A 35 (2002) 272

    Homogenization via formal multiscale asymptotics and volume averaging: How do the two techniques compare?

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    A wide variety of techniques have been developed to homogenize transport equations in multiscale and multiphase systems. This has yielded a rich and diverse field, but has also resulted in the emergence of isolated scientific communities and disconnected bodies of literature. Here, our goal is to bridge the gap between formal multiscale asymptotics and the volume averaging theory. We illustrate the methodologies via a simple example application describing a parabolic transport problem and, in so doing, compare their respective advantages/disadvantages from a practical point of view. This paper is also intended as a pedagogical guide and may be viewed as a tutorial for graduate students as we provide historical context, detail subtle points with great care, and reference many fundamental works

    Leaf litter traits of invasive alien species slow down decomposition compared to Spanish natives: a broad phylogenetic comparison.

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    Leaf traits related to the performance of invasive alien species can influence nutrient cycling through litter decomposition. However, there is no consensus yet about whether there are consistent differences in functional leaf traits between invasive and native species that also manifest themselves through their "after life" effects on litter decomposition. When addressing this question it is important to avoid confounding effects of other plant traits related to early phylogenetic divergences and to understand the mechanism underlying the observed results to predict which invasive species will exert larger effects on nutrient cycling. We compared initial leaf litter traits, and their effect on decomposability as tested in standardized incubations, in 19 invasive-native pairs of co-familial species from Spain. They included 12 woody and seven herbaceous alien species representative of the Spanish invasive flora. The predictive power of leaf litter decomposition rates followed the order: growth form > family > status (invasive vs. native) > leaf type. Within species pairs litter decomposition tended to be slower and more dependent on N and P in invaders than in natives. This difference was likely driven by the higher lignin content of invader leaves. Although our study has the limitation of not representing the natural conditions from each invaded community, it suggests a potential slowing down of the nutrient cycle at ecosystem scale upon invasion. © Springer-Verlag 2009
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