We consider a stochastic SIR system and we prove the existence, uniqueness and positivity of solution. Moreover the existence of an invariant measure under a suitable condition on the coefficients is studied.

Theory of chemical reactions in complex mixtures exhibits the following problem. Single reacting species follow an intrinsic kinetic law. However, the observable quantity, which is a mean of individual concentrations, follows a different law. This one is called «alias» of intrinsic kinetics. In this paper the phenomenon of alias of uniform families of differential equations is discussed in general terms.

We develop and test a relatively simple enhancement of the classical model reduction method applied to a class of chemical networks with mass conservation properties. Both the methods, being (i) the standard quasi-steady-state approximation method, and (ii) the novel so-called delayed quasi-steady-state approximation method, firstly proposed by Vejchodský (2014), are extensively presented. Both theoretical and numerical issues related to the setting of delays are discussed. Namely, for one slightly...

In this paper, we consider solutions to the following chemotaxis system with general sensitivity $$\left\{\begin{array}{c}\tau u_t=\Delta u-\nabla ·\left(u\nabla \chi \left(v\right)\right)\text{in}\Omega \times (0,\infty ),\hfill \\ \eta v_t=\Delta v-v+u\text{in}\Omega \times (0,\infty ),\hfill \\ {\displaystyle \frac{\partial u}{\partial \nu }=\frac{\partial u}{\partial \nu }=0\text{on}\partial \Omega \times (0,\infty ).}\hfill \end{array}\right.$$ Here, $\tau$ and $\eta$ are positive constants, $\chi$ is a smooth function on $(0,\infty )$ satisfying ${\chi }^{\text{'}}(·)>0$ and $\Omega$ is a bounded domain of ${𝐑}^n$ ($n\ge 2$). It is well known that the chemotaxis system with direct sensitivity ($\chi \left(v\right)={\chi }_{0}v$, ${\chi }_0>0$) has blowup solutions in the case where $n\ge 2$. On the other hand, in the case where $\chi \left(v\right)={\chi }_{0}logv$ with $0<{\chi }_0\ll 1$, any solution to the system exists globally in time and is bounded. We present a sufficient condition for the boundedness of...

In this paper a general class of Boltzmann-like bilinear integro-differential systems of equations (GKM, Generalized Kinetic Models) is considered. It is shown that their solutions can be approximated by the solutions of appropriate systems describing the dynamics of individuals undergoing stochastic interactions (at the "microscopic level"). The rate of approximation can be controlled. On the other hand the GKM result in various models known in biomathematics (at the "macroscopic level") including...

In a simple FitzHugh-Nagumo neuronal model with one fast and two slow variables, a sequence of period-doubling bifurcations for small-scale oscillations precedes the transition into the spiking regime. For a wide range of values of the timescale separation parameter, this scenario is recovered numerically. Its relation to the singularly perturbed integrable system is discussed.

This paper extends the volume filling chemotaxis model [18, 26] by taking into account the cell population interactions. The extended chemotaxis models have nonlinear diffusion and chemotactic sensitivity depending on cell population density, which is a modification of the classical Keller-Segel model in which the diffusion and chemotactic sensitivity are constants (linear). The existence and boundedness of global solutions of these models are discussed and...

The paper presents a new approach to fuzzy classification in the case of missing data. Rough-fuzzy sets are incorporated into logical type neuro-fuzzy structures and a rough-neuro-fuzzy classifier is derived. Theorems which allow determining the structure of the rough-neuro-fuzzy classifier are given. Several experiments illustrating the performance of the roughneuro-fuzzy classifier working in the case of missing features are described.

Many doctors believe that a patient will survive a heart attack unless a succeeding attack occurs in a week. Treating heart attacks as failures in Bernoulli trials we reduce the lifetime after a heart attack to the waiting time for the first failure followed by a success run shorter than a given k. In order to test the "true" critical period of the lifetime we need its distribution. The probability mass function and cumulative distribution function of the waiting time are expressed in explicit and...

Seeds of sunflowers are often modelled by $n⟼{\varphi }_{\theta }\left(n\right)=\sqrt{n}{e}^{2i\pi n\theta }$ leading to a roughly uniform repartition with seeds indexed by consecutive integers at angular distance $2\pi \theta$ for $\theta$ the golden ratio. We associate to such a map ${\varphi }_{\theta }$ a geodesic path ${\gamma }_{\theta }:{ℝ}_{\&gt;0}⟶{\mathrm{PSL}}_2\left(\mathbb{Z}\right)\setminus ℍ$ of the modular curve and use it for local descriptions of the image ${\varphi }_{\theta }\left(\mathbb{N}\right)$ of the phyllotactic map ${\varphi }_{\theta }$.

We investigate projective varieties which are binary symmetric models of trivalent phylogenetic trees. We prove that they have Gorenstein terminal singularities and are Fano varieties of index 4 and dimension equal to the number of edges of the tree in question. Moreover any two such varieties which are of the same dimension are deformation equivalent, that is, they are in the same connected component of the Hilbert scheme of the projective space. As an application we provide a simple formula for...