SearcharxivSearch

arXiv subjects

Haleh Ebadi

Publications and source records attributed to Haleh Ebadi.

4 recordsLinked to original sources

The strategy of survival for a competition between normal and anomalous diffusion

In this paper, we study the competition of two diffusion processes for achieving the maximum possible diffusion in an area. This competition, however, does not occur in the same circumstance; one of these processes is a normal diffusion with a higher growth rate, and another one is an anomalous diffusion with a lower growth rate. The trivial solution of the proposed model suggests that the winner is the one with the higher growth rate. But, the question is: what characteristics and strategies should the second diffusion include to prolong the survival in such a competition? The studied diffusion equations correspond to the SI model such that the anomalous diffusion has memory described by a fractional order derivative. The strategy promise that anomalous diffusion reaches maximum survival in case of forgetting some parts of the memory. This model can represent some of real phenomena, such as the contest of two companies in a market share, the spreading of two epidemic diseases, the diffusion of two species, or any reaction-diffusion related to real-world competition.

physics.soc-ph

Patterning the insect eye: from stochastic to deterministic mechanisms

While most processes in biology are highly deterministic, stochastic mechanisms are sometimes used to increase cellular diversity, such as in the specification of sensory receptors. In the human and Drosophila eye, photoreceptors sensitive to various wavelengths of light are distributed randomly across the retina. Mechanisms that underlie stochastic cell fate specification have been analysed in detail in the Drosophila retina. In contrast, the retinas of another group of dipteran flies exhibit highly ordered patterns. Species in the Dolichopodidae, the "long-legged" flies, have regular alternating columns of two types of ommatidia (unit eyes), each producing corneal lenses of different colours. Individual flies sometimes exhibit perturbations of this orderly pattern, with "mistakes" producing changes in pattern that can propagate across the entire eye, suggesting that the underlying developmental mechanisms follow local, cellular-automaton-like rules. We hypothesize that the regulatory circuitry patterning the eye is largely conserved among flies such that the difference between the Drosophila and Dolichopodidae eyes should be explicable in terms of relative interaction strengths, rather than requiring a rewiring of the regulatory network. We present a simple stochastic model which, among its other predictions, is capable of explaining both the random Drosophila eye and the ordered, striped pattern of Dolichopodidae.

q-bio.CB

Effect of memory in non-Markovian Boolean networks

One successful model of interacting biological systems is the Boolean network. The dynamics of a Boolean network, controlled with Boolean functions, is usually considered to be a Markovian (memory-less) process. However, both self organizing features of biological phenomena and their intelligent nature should raise some doubt about ignoring the history of their time evolution. Here, we extend the Boolean network Markovian approach: we involve the effect of memory on the dynamics. This can be explored by modifying Boolean functions into non-Markovian functions, for example, by investigating the usual non-Markovian threshold function, - one of the most applied Boolean functions. By applying the non-Markovian threshold function on the dynamical process of a cell cycle network, we discover a power law memory with a more robust dynamics than the Markovian dynamics.

q-bio.MN

Boolean networks with veto functions

Boolean networks are discrete dynamical systems for modeling regulation and signaling in living cells. We investigate a particular class of Boolean functions with inhibiting inputs exerting a veto (forced zero) on the output. We give analytical expressions for the sensitivity of these functions and provide evidence for their role in natural systems. In an intracellular signal transduction network [Helikar et al., PNAS (2008)], the functions with veto are over-represented by a factor exceeding the over-representation of threshold functions and canalyzing functions in the same system. In Boolean networks for control of the yeast cell cycle [Fangting Li et al., PNAS (2004), Davidich et al., PLoS One (2009)], none or minimal changes to the wiring diagrams are necessary to formulate their dynamics in terms of the veto functions introduced here.

q-bio.MN