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Exact low-temperature series expansion for the partition function of the zero-field Ising model on the infinite square lattice.

ABSTRACT: In this paper, we provide the exact expression for the coefficients in the low-temperature series expansion of the partition function of the two-dimensional Ising model on the infinite square lattice. This is equivalent to exact determination of the number of spin configurations at a given energy. With these coefficients, we show that the ferromagnetic-to-paramagnetic phase transition in the square lattice Ising model can be explained through equivalence between the model and the perfect gas of energy clusters model, in which the passage through the critical point is related to the complete change in the thermodynamic preferences on the size of clusters. The combinatorial approach reported in this article is very general and can be easily applied to other lattice models.

SUBMITTER: Siudem G

PROVIDER: S-EPMC5056370 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature

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Exact low-temperature series expansion for the partition function of the zero-field Ising model on the infinite square lattice.

Siudem Grzegorz G Fronczak Agata A Fronczak Piotr P

Scientific reports 20161010

In this paper, we provide the exact expression for the coefficients in the low-temperature series expansion of the partition function of the two-dimensional Ising model on the infinite square lattice. This is equivalent to exact determination of the number of spin configurations at a given energy. With these coefficients, we show that the ferromagnetic-to-paramagnetic phase transition in the square lattice Ising model can be explained through equivalence between the model and the perfect gas of ...[more]

PMID: 27721435

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Project description:BackgroundThroughout their lifespans, humans continually interact with the microbial world, including those organisms which live in and on the human body. Research in this domain has revealed the extensive links between the human-associated microbiota and health. In particular, the microbiota of the human gut plays essential roles in digestion, nutrient metabolism, immune maturation and homeostasis, neurological signaling, and endocrine regulation. Microbial interaction networks are frequently estimated from data and are an indispensable tool for representing and understanding the conditional correlation between the microbes. In this high-dimensional setting, zero-inflation and unit-sum constraint for relative abundance data pose challenges to the reliable estimation of microbial interaction networks.Methods and resultsTo identify the microbial interaction network, the zero-inflated latent Ising (ZILI) model is proposed which assumes the distribution of relative abundance relies only on finite latent states and provides a novel way to solve issues induced by the unit-sum and zero-inflation constrains. A two-step algorithm is proposed for the model selection of ZILI. ZILI is evaluated through simulated data and subsequently applied to an infant gut microbiota dataset from New Hampshire Birth Cohort Study. The results are compared with results from Gaussian graphical model (GGM) and dichotomous Ising model (DIS). Providing ZILI is the true data-generating model, the simulation studies show that the two-step algorithm can identify the graphical structure effectively and is robust to a range of parameter settings. For the infant gut microbiota dataset, the final estimated networks from GGM and ZILI turn out to have significant overlap in which the ZILI tends to select the sparser network than those from GGM. From the shared subnetwork, a hub taxon Lachnospiraceae is identified whose involvement in human disease development has been discovered recently in literature.ConclusionsConstrains induced by relative abundance of microbiota such as zero inflation and unit sum render the conditional correlation analysis unreliable for conventional methods such as GGM. The proposed optimal categoricalization based ZILI model provides an alternative yet elegant way to deal with these difficulties. The results from ZILI have reasonable biological interpretation. This model can also be used to study the microbial interaction in other body parts.

Project description:In analysis of multi-component complex systems, such as neural systems, identifying groups of units that share similar functionality will aid understanding of the underlying structures of the system. To find such a grouping, it is useful to evaluate to what extent the units of the system are separable. Separability or inseparability can be evaluated by quantifying how much information would be lost if the system were partitioned into subsystems, and the interactions between the subsystems were hypothetically removed. A system of two independent subsystems are completely separable without any loss of information while a system of strongly interacted subsystems cannot be separated without a large loss of information. Among all the possible partitions of a system, the partition that minimizes the loss of information, called the Minimum Information Partition (MIP), can be considered as the optimal partition for characterizing the underlying structures of the system. Although the MIP would reveal novel characteristics of the neural system, an exhaustive search for the MIP is numerically intractable due to the combinatorial explosion of possible partitions. Here, we propose a computationally efficient search to precisely identify the MIP among all possible partitions by exploiting the submodularity of the measure of information loss, when the measure of information loss is submodular. Submodularity is a mathematical property of set functions which is analogous to convexity in continuous functions. Mutual information is one such submodular information loss function, and is a natural choice for measuring the degree of statistical dependence between paired sets of random variables. By using mutual information as a loss function, we show that the search for MIP can be performed in a practical order of computational time for a reasonably large system (N = 100 ? 1000). We also demonstrate that MIP search allows for the detection of underlying global structures in a network of nonlinear oscillators.

Dataset Information

Exact low-temperature series expansion for the partition function of the zero-field Ising model on the infinite square lattice.

Publications

Exact low-temperature series expansion for the partition function of the zero-field Ising model on the infinite square lattice.

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