Competition between biological species in marine environments is affected by the motion of the surrounding fluid. An effective 2D compressibility can arise, for example, from the convergence and divergence of water masses at the depth at which passively traveling photosynthetic organisms are restricted to live. In this report, we seek to quantitatively study genetics under flow. To this end, we couple an off-lattice agent-based simulation of two populations in 1D to a weakly compressible velocity field--first a sine wave and then a shell model of turbulence.

We consider a nonlinear system of partial differential equations which describes the dynamics of two types of cell densities with contact inhibition. After a change of variables the system turns out to be parabolic-hyperbolic and admits travelling wave solutions which solve a 3D dynamical system. Compared to the scalar Fisher-KPP equation, the structure of the travelling wave solutions is surprisingly rich and to unravel part of it is the aim of the present paper. In particular, we consider a parameter regime where the minimal wave velocity of the travelling wave solutions is negative.

The evolution of a geothermal system is studied. A mathematical model is proposed and the corresponding free boundary problem is formulated in a one-dimensional geometry. A situation corresponding to the geothermal field in Larderello, Tuscany (Italy) is considered, showing that the problem has two characteristic time scales, related to the motion of interface and diffusion of vapor.

GPU version of AMG preconditioner

In Rayleigh-Bénard convection (RBC) for fluids with Prandtl number Pr1, rotation beyond a critical (small) rotation rate is known to cause a sudden enhancement of heat transfer, which can be explained by a change in the character of the boundary layer (BL) dynamics near the top and bottom plates of the convection cell. Namely, with increasing rotation rate, the BL signature suddenly changes from Prandtl-Blasius type to Ekman type.

Human mesenchymal/stromal stem cells (hMSC) are the most promising cell source for adult cell therapies in regenerative medicine. Many clinical trials have reported the use of autologous transplantation of hMSCs in several disorders, but with limited results. To exert their potential, hMSCs could exhibit efficient homing and migration toward lesion sites among other effects, but the underlying process is not clear enough. To further increase the knowledge, we studied the co-regulation between hypoxia-regulated genes and miRNAs.