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13th International Conference on Membrane Computing - MTA Sztaki

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T. Hinze, B. Schell, M. Schumann, C. Bodenstein<br />

see Figure 10. Obviously, the reacti<strong>on</strong> network attempts to calculate the next<br />

step but is unable to do so in time for the next count. This effect preserves for<br />

any rate c<strong>on</strong>stant k0.9, there<br />

is no restricti<strong>on</strong> in the frequency divider’s functi<strong>on</strong>ality.<br />

Finally, let us return to the life<br />

cycle of periodical cicadas which<br />

gave the crucial inspirati<strong>on</strong> for our<br />

studies. We are aware that the<br />

mechanisms evolved in this life<br />

form are most probably far away<br />

from a binary counter modulo 17.<br />

Up to now, we failed in retrieving<br />

any scientific publicati<strong>on</strong> <strong>on</strong> potential<br />

or even verified mechanisms. A<br />

more or less speculative hypothesis<br />

aims at a combinati<strong>on</strong> of two processes,<br />

a slow growth <strong>on</strong> the <strong>on</strong>e<br />

hand and a threshold <strong>on</strong> the other.<br />

Growth means a successive accumulati<strong>on</strong><br />

of a dedicated species. As<br />

so<strong>on</strong> as its c<strong>on</strong>centrati<strong>on</strong> exceeds<br />

T<br />

1 B<br />

c<strong>on</strong>centrati<strong>on</strong> (a.u.)<br />

1<br />

0.8<br />

0.6<br />

0.4<br />

0.2<br />

C<br />

0<br />

0 1000 2000 3000 4000 5000<br />

time (a.u.)<br />

Fig. 10. Dynamical behaviour of the original<br />

frequency divider model 1:17 after slowing<br />

down all reacti<strong>on</strong>s within the logical unit for<br />

<strong>on</strong>e order of magnitude<br />

an inherently set threshold, the finalisati<strong>on</strong> of the life cycle is initialised indicating<br />

the elapsed amount of 17 years. A successive accumulati<strong>on</strong> organised for<br />

instance in annual cycles is useful for a high precisi<strong>on</strong>. To this end, a core oscillator<br />

could provide an annually altering signal of the form a +sin(bt) subject to<br />

time t. A simple signal integrati<strong>on</strong> then produces a temporal course of the form<br />

at + c · sin(bt + d) with a successive, staircase-shaped growth. Nevertheless, this<br />

strategy is more pr<strong>on</strong>e to premature or late alert than an n-ary counter.<br />

4 Core Oscillator’s Interplay in Suprachiasmatic Nucleus<br />

A sec<strong>on</strong>d applicati<strong>on</strong> study is intended to dem<strong>on</strong>strate in brief the descripti<strong>on</strong>al<br />

capacity of our P meta framework. Let us c<strong>on</strong>sider the suprachiasmatic nucleus,<br />

a regi<strong>on</strong> of the human brain, in which each neur<strong>on</strong> comprises a core oscillator<br />

for generati<strong>on</strong> of a circadian rhythm characterised by a c<strong>on</strong>trollable period close<br />

to 24 hours. A cyclic gene regulatory network c<strong>on</strong>sisting of 10 molecular species<br />

and 18 reacti<strong>on</strong>s including an inhibitory negative feedback forms this core oscillator<br />

whose dynamical behaviour had been formalised via specific ODEs based<br />

<strong>on</strong> mass-acti<strong>on</strong> and sec<strong>on</strong>d-order Hill kinetics. For a full descripti<strong>on</strong>, we refer<br />

to [3]. The neur<strong>on</strong>al core oscillators within the suprachiasmatic nucleus appear<br />

to be hierarchically organised in several layers. A small group of independently<br />

oscillating neur<strong>on</strong>s c<strong>on</strong>stitutes the so-called master-clock layer. Neur<strong>on</strong>s in down-<br />

238

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