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13th International Conference on Membrane Computing - MTA Sztaki

13th International Conference on Membrane Computing - MTA Sztaki

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L.F. Macías-Ramos, M.J. Pérez-Jiménez, A. Riscos-Núñez, M. Rius-F<strong>on</strong>t,<br />

L. Valencia-Cabrera<br />

in polynomial time by using some kind of rules, and then massive parallelism<br />

is used to simultaneously check all the candidate soluti<strong>on</strong>s. Inspired by living<br />

cells, several ways for obtaining exp<strong>on</strong>ential workspace in polynomial time were<br />

proposed: membrane divisi<strong>on</strong> (mitosis) [16], membrane creati<strong>on</strong> (autopoiesis) [7],<br />

and membrane separati<strong>on</strong> (membrane ssi<strong>on</strong>) [12]. These three ways have given<br />

rise to the following models: P systems with active membranes, P systems with<br />

membrane creati<strong>on</strong>, and P systems with membrane separati<strong>on</strong>.<br />

A new type of P systems, the so-called tissue P systems, was c<strong>on</strong>sidered<br />

in [10]. Instead of c<strong>on</strong>sidering a hierarchical arrangement, membranes/cells are<br />

placed in the nodes of a virtual graph. This variant has two biological justicati<strong>on</strong>s<br />

(see [11]): intercellular communicati<strong>on</strong> and cooperati<strong>on</strong> between neur<strong>on</strong>s.<br />

The comm<strong>on</strong> mathematical model of these two mechanisms is a net of processors<br />

dealing with symbols and communicating these symbols al<strong>on</strong>g channels speci-<br />

ed in advance. The communicati<strong>on</strong> am<strong>on</strong>g cells is based <strong>on</strong> symport/antiport<br />

rules, which were introduced to P systems in [18]. These models have a special<br />

alphabet associated with the envir<strong>on</strong>ment of the system and it is assumed that<br />

the symbols of that alphabet appear in an arbitrary large amount of copies at<br />

the initial c<strong>on</strong>gurati<strong>on</strong> of the system.<br />

From the seminal deniti<strong>on</strong>s of tissue P systems [10, 11], several research lines<br />

have been developed and other variants have arisen (see, for example, [1, 2, 4, 8,<br />

9, 14]). One of the most interesting variants of tissue P systems was presented<br />

in [19], where the deniti<strong>on</strong> of tissue P systems is combined with the <strong>on</strong>e of P<br />

systems with active membranes, yielding tissue P systems with cell divisi<strong>on</strong>.<br />

In the biological phenomen<strong>on</strong> of ssi<strong>on</strong>, the c<strong>on</strong>tents of the two new cells<br />

evolved from a cell can be signicantly dierent, and membrane separati<strong>on</strong> inspired<br />

by this biological phenomen<strong>on</strong> in the framework of cell-like P systems<br />

was proved to be an ecient way to obtain exp<strong>on</strong>ential workspace in polynomial<br />

time [12]. In [13], a new class of tissue P systems based <strong>on</strong> cell ssi<strong>on</strong>, called tissue<br />

P systems with cell separati<strong>on</strong>, was presented. Its computati<strong>on</strong>al eciency<br />

was investigated, and two important results were obtained: (a) <strong>on</strong>ly tractable<br />

problems can be eciently solved by using cell separati<strong>on</strong> and communicati<strong>on</strong><br />

rules with length at most 1, and (b) an ecient (uniform) soluti<strong>on</strong> to the SAT<br />

problem by using cell separati<strong>on</strong> and communicati<strong>on</strong> rules with length at most<br />

8 was presented.<br />

In this paper we study the eciency of tissue P systems with communicati<strong>on</strong><br />

rules and cell separati<strong>on</strong> where the alphabet associated with the envir<strong>on</strong>ment<br />

is empty. These systems are called tissue P systems without envir<strong>on</strong>ment and,<br />

specically, we prove that <strong>on</strong>ly tractable problems can be solved in polynomial<br />

time by families of tissue P systems with communicati<strong>on</strong> rules, with cell separati<strong>on</strong><br />

and without envir<strong>on</strong>ment.<br />

The paper is organized as follows: rst, we recall some preliminaries, and<br />

then, the deniti<strong>on</strong> of tissue P systems with cell separati<strong>on</strong>, recognizer tissue<br />

P systems and computati<strong>on</strong>al complexity classes in this framework, are briey<br />

described. Secti<strong>on</strong> 4 is devoted to the main result of the paper: the polynomial<br />

278

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