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At least 217 records · Page 12Linked to original sources

arXiv2001

Justification of Sexual Reproduction by Modified Penna Model of Ageing

We generalize the standard Penna bit-string model of biological ageing by assuming that each deleterious mutation diminishes the survival probability in every time interval by a small percentage. This effect is added to the usual lethal but age-dependent effect of the same mutation. We then find strong advantages or disadvantages of sexual reproduction (with males and females) compared to asexual cloning, depending on parameters.

cond-mat.stat-mech↗

arXiv2001

Phenomenological Theory of Survival

Theoretical analysis proves that human survivability is dominated by an unusual physical, rather than biological, mechanism, which yields an exact law. The law agrees with all experimental data, but, contrary to existing theories, it is the same for an entire species, i.e., it is independent of the population, its phenotypes, environment and history. The law implies that the survivability changes with environment via phase transitions, which are simultaneous for all generations. They allow for a rapid (within few percent of the life span) and significant increase in the life expectancy even above its value at a much earlier age.

physics.bio-ph↗

arXiv2001

Simulated emergence of cyclic sexual-asexual reproduction

Motivated by the cyclic pattern of reproductive regimes observed in some species of green flies (``{\it aphids}''), we simulate the evolution of a population enduring harsh seasonal conditions for survival. The reproductive regime of each female is also seasonal in principle and genetically acquired, and can mutate for each newborn with some small probability. The results show a sharp transition at a critical value of the survival probability in the winter, between a reproductive regime in the fall that is predominantly sexual, for low values of this probability, or asexual, for high values.

cond-mat.stat-mech↗

arXiv2001

Multifractal characterisation of length sequences of coding and noncoding segments in a complete genome

The coding and noncoding length sequences constructed from a complete genome are characterised by multifractal analysis. The dimension spectrum $D_{q}$ and its derivative, the 'analogous' specific heat $C_{q}$, are calculated for the coding and noncoding length sequences of bacteria, where $q$ is the moment order of the partition sum of the sequences. From the shape of the $% D_{q}$ and $C_{q}$ curves, it is seen that there exists a clear difference between the coding/noncoding length sequences of all organisms considered and a completely random sequence. The complexity of noncoding length sequences is higher than that of coding length sequences for bacteria. Almost all $D_{q}$ curves for coding length sequences are flat, so their multifractality is small whereas almost all $D_{q}$ curves for noncoding length sequences are multifractal-like. We propose to characterise the bacteria according to the types of the $C_{q}$ curves of their noncoding length sequences.

physics.bio-ph↗

arXiv2002

Retrieval and Chaos in Extremely Diluted Non-Monotonic Neural Networks

We discuss, in this paper, the dynamical properties of extremely diluted, non-monotonic neural networks. Assuming parallel updating and the Hebb prescription for the synaptic connections, a flow equation for the macroscopic overlap is derived. A rich dynamical phase diagram was obtained, showing a stable retrieval phase, as well as a cycle two and chaotic behavior. Numerical simulations were performed, showing good agreement with analytical results. Furthermore, the simulations give an additional insight into the microscopic dynamical behavior during the chaotic phase. It is shown that the freezing of individual neuron states is related to the structure of chaotic attractors.

cond-mat.dis-nn↗

arXiv2002

How the Quasispecies Evolution Depends on the Topology of the Genome Space

We compared the properties of the error threshold transition in quasispecies evolution for three different topologies of the genome space. They are a) hypercube b) rugged landscape modelled by an ultrametric space, and c) holey landscape modelled by Bethe lattice. In all studied topologies the phase transition exists. We calculated the critical exponents in all the cases. For the critical exponent corresponding to appropriately defined susceptibility we found super-universal value.

cond-mat.stat-mech↗

arXiv2003

Networks in life: Scaling properties and eigenvalue spectra

We analyse growing networks ranging from collaboration graphs of scientists to the network of similarities defined among the various transcriptional profiles of living cells. For the explicit demonstration of the scale-free nature and hierarchical organization of these graphs, a deterministic construction is also used. We demonstrate the use of determining the eigenvalue spectra of sparse random graph models for the categorization of small measured networks.

cond-mat.stat-mech↗

arXiv2002

Learning by a nerual net in a noisy environment - The pseudo-inverse solution revisited

A recurrent neural net is described that learns a set of patterns in the presence of noise. The learning rule is of Hebbian type, and, if noise would be absent during the learning process, the resulting final values of the weights would correspond to the pseudo-inverse solution of the fixed point equation in question. For a non-vanishing noise parameter, an explicit expression for the expectation value of the weights is obtained. This result turns out to be unequal to the pseudo-inverse solution. Furthermore, the stability properties of the system are discussed.

cond-mat.dis-nn↗

arXiv2002

Anomalous diffusion on dynamical networks: A model for interacting epithelial cell migration

We propose a model for cell migration where epithelial cells are able to detect trajectories of other cells and try to follow them. As cells move along in 2D cell culture, they mark their paths by loosing tiny parts of cytoplasm. Any cell moving on a surface where other cells have moved before faces a network of cell trajectories, which it tries to restrict its motion onto. With the Tsallis modification of classical thermodynamics one can solve the relevant Fokker-Planck like equation and obtain experimentally testable distribution functions. We compare the model to experimental data of normal mammary epithelial cells and cells which have been genetically manipulated to change their degree of cell-cell interaction.

cond-mat↗

arXiv2002

Adaptation using hybridized genetic crossover strategies

We present a simple game which mimics the complex dynamics found in most natural and social systems. Intelligent players modify their strategies periodically, depending on their performances. We propose that the agents use hybridized one-point genetic crossover mechanism,inspired by genetic evolution in biology, to modify the strategies and replace the bad strategies. We study the performances of the agents under different conditions and investigate how they adapt themselves in order to survive or be the best, by finding new strategies using the highly effective mechanism we proposed.

cond-mat.stat-mech↗

arXiv2002

Observation of Mammalian Similarity Through Allometric Scaling Laws

We discuss the problem of observation of natural similarity in skeletal evolution of terrestrial mammals. Analysis is given by means of testing of the power scaling laws established in long bone allometry, which describe development of bones (of length $L$ and diameter $D$) with body mass in terms of the growth exponents, \QTR{it}{e.g.} $λ=d\log L/d\log D$. The bone-size evolution scenario given three decades ago by McMahon was quiet explicit on the geometrical-shape and mechanical-force constraints that predicted $λ=2/3$. This remains too far from the mammalian allometric exponent $λ^{(\exp)}=0.80\pm 0.2$, recently revised by Christiansen, that is a chief puzzle in long bone allometry. We give therefore new insights into McMahon's constraints and report on the first observation of the critical-elastic-force, bending-deformation, muscle-induced mechanism that underlies the allometric law with estimated $λ=0.80\pm 0.3$. This mechanism governs the bone-size evolution with avoiding skeletal fracture caused by muscle-induced peak stresses and is expected to be unique for small and large mammals.

physics.bio-ph↗

arXiv2003

A model of population dynamics - further investigations

The population is composed of individuals characterised by their genetic strings, phenotypes and ages. We discuss the influence of probabilities of survival of the individuals on the dynamics and phenotypic variability of the population. We show that constant survival probabilities of individuals are propitious for preserving phenotypic variability of the population. For constant survival probabilities oscillations of 'the average fitness' of the population and normal distributions of the phenotypes are observed. When the probabilities of survival are directly proportinal to the individuals' adaptations the population can reach the maximum possible average adaptation, but the phenotypic variability of the population is completely lost and oscillations of 'the average fitness' of the population do not occur. We also investigate the behaviour of the population caused by the probabilities of survival that partly depend on the individuals' adaptations. The role of the length of the individuals' genetic strings is considered here.

physics.bio-ph↗

arXiv2003

Promiscuity and the Evolution of Sexual Transmitted Diseases

We study the relation between different social behaviors and the onset of epidemics in a model for the dynamics of sexual transmitted diseases. The model considers the society as a system of individual sexuated agents that can be organized in couples and interact with each other. The different social behaviors are incorporated assigning what we call a promiscuity value to each individual agent. The individual promiscuity is taken from a distributions and represents the daily probability of going out to look for a sexual partner, abandoning its eventual mate. In terms of this parameter we find a threshold for the epidemic which is much lower than the classical fully mixed model prediction, i.e. $R_0$ (basic reproductive number) $= 1$. Different forms for the distribution of the population promiscuity are considered showing that the threshold is weakly sensitive to them. We study the homosexual and the heterosexual case as well.

nlin.AO↗

arXiv1998

Hydrodynamics of bacterial motion

In this paper we present a hydrodynamic approach to describe the motion of migrating bacteria as a special class of self-propelled systems. Analytical and numerical calculations has been performed to study the behavior of our model in the turbulent-like regime and to show that a phase transition occurs as a function of noise strength. Our results can explain previous experimental observations as well as results of numerical simulations.

cond-mat.soft↗

arXiv1997

Transition between immune and disease states in a cellular automaton model of clonal immune response

In this paper we extend the Celada-Seiden (CS) model of the humoral immune response to include infectious virus and cytotoxic T lymphocytes (cellular response). The response of the system to virus involves a competition between the ability of the virus to kill the host cells and the host's ability to eliminate the virus. We find two basins of attraction in the dynamics of this system, one is identified with disease and the other with the immune state. There is also an oscillating state that exists on the border of these two stable states. Fluctuations in the population of virus or antibody can end the oscillation and drive the system into one of the stable states. The introduction of mechanisms of cross-regulation between the two responses can bias the system towards one of them. We also study a mean field model, based on coupled maps, to investigate virus-like infections. This simple model reproduces the attractors for average populations observed in the cellular automaton. All the dynamical behavior connected to spatial extension is lost, as is the oscillating feature. Thus the mean field approximation introduced with coupled maps destroys oscillations.

chao-dyn↗

arXiv1998

Realistic Models of Biological Motion

The origin of biological motion can be traced back to the function of molecular motor proteins. Cytoplasmic dynein and kinesin transport organelles within our cells moving along a polymeric filament, the microtubule. The motion of the myosin molecules along the actin filaments is responsible for the contraction of our muscles. Recent experiments have been able to reveal some important features of the motion of individual motor proteins, and a new statistical physical description - often referred to as ``thermal ratchets'' - has been developed for the description of motion of these molecules. In this approach the motors are considered as Brownian particles moving along one-dimensional periodic structures due to the effect of nonequilibrium fluctuations. Assuming specific types of interaction between the particles the models can be made more realistic. We have been able to give analytic solutions for our model of kinesin with elastically coupled Brownian heads and for the motion of the myosin filament where the motors are connected through a rigid backbone. Our theoretical predictions are in a very good agreement with the various experimental results. In addition, we have considered the effects arising as a result of interaction among a large number of molecular motors, leading to a number of novel cooperative transport phenomena.

cond-mat.stat-mech↗

arXiv1998

A hierarchical scheme for cooperativity and folding in proteins

We propose a protein model based on a hierarchy of constraints that force the protein to follow certain pathways when changing conformation. The model exhibits a first order phase transition, cooperativity and is exactly solvable. It also shows an unexpected symmetry between folding and unfolding pathways as suggested by a recent experiment.

cond-mat↗

arXiv1997

Wilson renormalization of a reaction-diffusion process

Healthy and sick individuals (A and B particles) diffuse independently with diffusion constants D_A and D_B. Sick individuals upon encounter infect healthy ones (at rate k), but may also spontaneously recover (at rate 1/τ). The propagation of the epidemic therefore couples to the fluctuations in the total population density. Global extinction occurs below a critical value ρ_{c} of the spatially averaged total density. The epidemic evolves as the diffusion--reaction--decay process A + B --> 2B, B --> A , for which we write down the field theory. The stationary state properties of this theory when D_A=D_B were obtained by Kree et al. The critical behavior for D_A D_B remains unsolved.

cond-mat.stat-mech↗