9,880 research outputs found

    Spontaneous structure formation in a network of chaotic units with variable connection strengths

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    As a model of temporally evolving networks, we consider a globally coupled logistic map with variable connection weights. The model exhibits self-organization of network structure, reflected by the collective behavior of units. Structural order emerges even without any inter-unit synchronization of dynamics. Within this structure, units spontaneously separate into two groups whose distinguishing feature is that the first group possesses many outwardly-directed connections to the second group, while the second group possesses only few outwardly-directed connections to the first. The relevance of the results to structure formation in neural networks is briefly discussed.Comment: 4 pages, 3 figures, REVTe

    Multifractal analysis of nonhyperbolic coupled map lattices: Application to genomic sequences

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    Symbolic sequences generated by coupled map lattices (CMLs) can be used to model the chaotic-like structure of genomic sequences. In this study it is shown that diffusively coupled Chebyshev maps of order 4 (corresponding to a shift of 4 symbols) very closely reproduce the multifractal spectrum DqD_q of human genomic sequences for coupling constant α=0.35±0.01\alpha =0.35\pm 0.01 if q>0q>0. The presence of rare configurations causes deviations for q<0q<0, which disappear if the rare event statistics of the CML is modified. Such rare configurations are known to play specific functional roles in genomic sequences serving as promoters or regulatory elements.Comment: 7 pages, 6 picture

    Self-organized and driven phase synchronization in coupled maps

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    We study the phase synchronization and cluster formation in coupled maps on different networks. We identify two different mechanisms of cluster formation; (a) {\it Self-organized} phase synchronization which leads to clusters with dominant intra-cluster couplings and (b) {\it driven} phase synchronization which leads to clusters with dominant inter-cluster couplings. In the novel driven synchronization the nodes of one cluster are driven by those of the others. We also discuss the dynamical origin of these two mechanisms for small networks with two and three nodes.Comment: 4 pages including 2 figure

    Long transients and cluster size in globally coupled maps

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    We analyze the asymptotic states in the partially ordered phase of a system of globally coupled logistic maps. We confirm that, regardless of initial conditions, these states consist of a few clusters, and they properly belong in the ordered phase of these systems. The transient times necessary to reach the asymptotic states can be very long, especially very near the transition line separating the ordered and the coherent phases. We find that, where two clusters form, the distribution of their sizes corresponds to windows of regular or narrow-band chaotic behavior in the bifurcation diagram of a system of two degrees of freedom that describes the motion of two clusters, where the size of one cluster acts as a bifurcation parameter.Comment: To appear in Europhysics Letter

    Recursiveness, Switching, and Fluctuations in a Replicating Catalytic Network

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    A protocell model consisting of mutually catalyzing molecules is studied in order to investigate how chemical compositions are transferred recursively through cell divisions under replication errors. Depending on the path rate, the numbers of molecules and species, three phases are found: fast switching state without recursive production, recursive production, and itinerancy between the above two states. The number distributions of the molecules in the recursive states are shown to be log-normal except for those species that form a core hypercycle, and are explained with the help of a heuristic argument.Comment: 4 pages (with 7 figures (6 color)), submitted to PR

    Origin of complexity in multicellular organisms

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    Through extensive studies of dynamical system modeling cellular growth and reproduction, we find evidence that complexity arises in multicellular organisms naturally through evolution. Without any elaborate control mechanism, these systems can exhibit complex pattern formation with spontaneous cell differentiation. Such systems employ a `cooperative' use of resources and maintain a larger growth speed than simple cell systems, which exist in a homogeneous state and behave 'selfishly'. The relevance of the diversity of chemicals and reaction dynamics to the growth of a multicellular organism is demonstrated. Chaotic biochemical dynamics are found to provide the multi-potency of stem cells.Comment: 6 pages, 2 figures, Physical Review Letters, 84, 6130, (2000

    K_l3 form factor with two-flavors of dynamical domain-wall quarks

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    We report on our calculation of K \to \pi vector form factor by numerical simulations of two-flavor QCD on a 16^3x32x12 lattice at a \simeq 0.12 fm using domain-wall quarks and DBW2 glue. Our preliminary result at a single sea quark mass correponding to m_PS/m_V \simeq 0.53 shows a good agreement with previous estimate in quenched QCD and that from a phenomenological model.Comment: 6 pages, 5 figures, poster presented at Lattice2005 (Weak matrix elements); v2: a reference adde

    Steady-state stabilization due to random delays in maps with self-feedback loops and in globally delayed-coupled maps

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    We study the stability of the fixed-point solution of an array of mutually coupled logistic maps, focusing on the influence of the delay times, Ď„ij\tau_{ij}, of the interaction between the iith and jjth maps. Two of us recently reported [Phys. Rev. Lett. {\bf 94}, 134102 (2005)] that if Ď„ij\tau_{ij} are random enough the array synchronizes in a spatially homogeneous steady state. Here we study this behavior by comparing the dynamics of a map of an array of NN delayed-coupled maps with the dynamics of a map with NN self-feedback delayed loops. If NN is sufficiently large, the dynamics of a map of the array is similar to the dynamics of a map with self-feedback loops with the same delay times. Several delayed loops stabilize the fixed point, when the delays are not the same; however, the distribution of delays plays a key role: if the delays are all odd a periodic orbit (and not the fixed point) is stabilized. We present a linear stability analysis and apply some mathematical theorems that explain the numerical results.Comment: 14 pages, 13 figures, important changes (title changed, discussion, figures, and references added
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