26 research outputs found

    箱とバスケットと玉の系におけるソリトン解

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    九州大学応用力学研究所研究集会報告 No.23AO-S7 「非線形波動研究の進展 : 現象と数理の相互作用」Report of RIAM Symposium No.23AO-S7 Progress in nonlinear wave : interaction between experimental and mathematical aspects箱とバスケットと玉の系における超離散双線形形式およびソリトン解などについて,得られた結果を報告する

    Entanglement Cost of Antisymmetric States and Additivity of Capacity of Some Quantum Channel

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    We study the entanglement cost of the states in the contragredient space, which consists of (d1)(d-1) dd-dimensional systems. The cost is always log2(d1)\log_2 (d-1) ebits when the state is divided into bipartite \C^d \otimes (\C^d)^{d-2}. Combined with the arguments in \cite{Matsumoto02}, additivity of channel capacity of some quantum channels is also shown.Comment: revtex 4 pages, no figures, small changes in title and author's affiliation and some typo are correcte

    Fundamental Cycle of a Periodic Box-Ball System

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    We investigate a soliton cellular automaton (Box-Ball system) with periodic boundary conditions. Since the cellular automaton is a deterministic dynamical system that takes only a finite number of states, it will exhibit periodic motion. We determine its fundamental cycle for a given initial state.Comment: 28 pages, 6 figure

    On a Periodic Soliton Cellular Automaton

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    We propose a box and ball system with a periodic boundary condition (pBBS). The time evolution rule of the pBBS is represented as a Boolean recurrence formula, an inverse ultradiscretization of which is shown to be equivalent with the algorithm of the calculus for the 2Nth root. The relations to the pBBS of the combinatorial R matrix of Uq(AN(1)){U'}_q(A_N^{(1)}) are also discussed.Comment: 17 pages, 5 figure

    Entanglement Cost of Three-Level Antisymmetric States

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    We show that the entanglement cost of the three-dimensional antisymmetric states is one ebit.Comment: 8page

    Cohesive and Anisotropic Vascular Endothelial Cell Motility Driving Angiogenic Morphogenesis

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    Vascular endothelial cells (ECs) in angiogenesis exhibit inhomogeneous collective migration called “cell mixing”, in which cells change their relative positions by overtaking each other. However, how such complex EC dynamics lead to the formation of highly ordered branching structures remains largely unknown. To uncover hidden laws of integration driving angiogenic morphogenesis, we analyzed EC behaviors in an in vitro angiogenic sprouting assay using mouse aortic explants in combination with mathematical modeling. Time-lapse imaging of sprouts extended from EC sheets around tissue explants showed directional cohesive EC movements with frequent U-turns, which often coupled with tip cell overtaking. Imaging of isolated branches deprived of basal cell sheets revealed a requirement of a constant supply of immigrating cells for ECs to branch forward. Anisotropic attractive forces between neighboring cells passing each other were likely to underlie these EC motility patterns, as evidenced by an experimentally validated mathematical model. These results suggest that cohesive movements with anisotropic cell-to-cell interactions characterize the EC motility, which may drive branch elongation depending on a constant cell supply. The present findings provide novel insights into a cell motility-based understanding of angiogenic morphogenesis
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