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Register a new userOn the Complexity of the Stability Problem of Binary Freezing Totalistic Cellular Automata
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Added by
Diego Maldonado
Publication date
2019
fields
Informatics Engineering
and research's language is
English
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In this paper we study the family of two-state Totalistic Freezing Cellular Automata (TFCA) defined over the triangular and square grids with von Neumann neighborhoods. We say that a Cellular Automaton is Freezing and Totalistic if the active cells remain unchanged, and the new value of an inactive cell depends only on the sum of its active neighbors. We classify all the Cellular Automata in the class of TFCA, grouping them in five different classes: the Trivial rules, Turing Universal rules,Algebraic rules, Topological rules and Fractal Growing rules. At the same time, we study in this family the Stability problem, consisting in deciding whether an inactive cell becomes active, given an initial configuration.We exploit the properties of the automata in each group to show that: - For Algebraic and Topological Rules the Stability problem is in $text{NC}$. - For Turing Universal rules the Stability problem is $text{P}$-Complete.
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In this paper we study the family of freezing cellular automata (FCA) in the context of asynchronous updating schemes. A cellular automaton is called freezing if there exists an order of its states, and the transitions are only allowed to go from a lower to a higher state. A cellular automaton is asynchronous if at each time-step only one cell is updated. Given configuration, we say that a cell is unstable if there exists a sequential updating scheme that changes its state. In this context, we define the problem AsyncUnstability, which consists in deciding if a cell is unstable or not. In general AsyncUnstability is in NP, and we study in which cases we can solve the problem by a more efficient algorithm. We begin showing that AsyncUnstability is in NL for any one-dimensional FCA. Then we focus on the family of life-like freezing CA (LFCA), which is a family of two-dimensional two-state FCA that generalize the freezing version of the game of life, known as life without death. We study the complexity of AsyncUnstability for all LFCA in the triangular and square grids, showing that almost all of them can be solved in NC, except for one rule for which the problem is NP-complete.
We present an intuitive formalism for implementing cellular automata on arbitrary topologies. By that means, we identify a symmetry operation in the class of elementary cellular automata. Moreover, we determine the subset of topologically sensitive elementary cellular automata and find that the overall number of complex patterns decreases under increasing neighborhood size in regular graphs. As exemplary applications, we apply the formalism to complex networks and compare the potential of scale-free graphs and metabolic networks to generate complex dynamics.
This paper studies three classes of cellular automata from a computational point of view: freezing cellular automata where the state of a cell can only decrease according to some order on states, cellular automata where each cell only makes a bounded number of state changes in any orbit, and finally cellular automata where each orbit converges to some fixed point. Many examples studied in the literature fit into these definitions, in particular the works on cristal growth started by S. Ulam in the 60s. The central question addressed here is how the computational power and computational hardness of basic properties is affected by the constraints of convergence, bounded number of change, or local decreasing of states in each cell. By studying various benchmark problems (short-term prediction, long term reachability, limits) and considering various complexity measures and scales (LOGSPACE vs. PTIME, communication complexity, Turing computability and arithmetical hierarchy) we give a rich and nuanced answer: the overall computational complexity of such cellular automata depends on the class considered (among the three above), the dimension, and the precise problem studied. In particular, we show that all settings can achieve universality in the sense of Blondel-Delvenne-Kr{u}rka, although short term predictability varies from NLOGSPACE to P-complete. Besides, the computability of limit configurations starting from computable initial configurations separates bounded-change from convergent cellular automata in dimension 1, but also dimension 1 versus higher dimensions for freezing cellular automata. Another surprising dimension-sensitive result obtained is that nilpotency becomes decidable in dimension 1 for all the three classes, while it stays undecidable even for freezing cellular automata in higher dimension.
We prove several results about the complexity of the role colouring problem. A role colouring of a graph $G$ is an assignment of colours to the vertices of $G$ such that two vertices of the same colour have identical sets of colours in their neighbourhoods. We show that the problem of finding a role colouring with $1< k <n$ colours is NP-hard for planar graphs. We show that restricting the problem to trees yields a polynomially solvable case, as long as $k$ is either constant or has a constant difference with $n$, the number of vertices in the tree. Finally, we prove that cographs are always $k$-role-colourable for $1<kleq n$ and construct such a colouring in polynomial time.
The paper proposes a simple formalism for dealing with deterministic, non-deterministic and stochastic cellular automata in a unifying and composable manner. Armed with this formalism, we extend the notion of intrinsic simulation between deterministic cellular automata, to the non-deterministic and stochastic settings. We then provide explicit tools to prove or disprove the existence of such a simulation between two stochastic cellular automata, even though the intrinsic simulation relation is shown to be undecidable in dimension two and higher. The key result behind this is the caracterization of equality of stochastic global maps by the existence of a coupling between the random sources. We then prove that there is a universal non-deterministic cellular automaton, but no universal stochastic cellular automaton. Yet we provide stochastic cellular automata achieving optimal partial universality.
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