Individual based and mean-field modeling of direct aggregation.

We introduce two models of biological aggregation, based on randomly moving particles with individual stochasticity depending on the perceived average population density in their neighborhood. In the first-order model the location of each individual is subject to a density-dependent random walk, while in the second-order model the density-dependent random walk acts on the velocity variable, together with a density-dependent damping term. The main novelty of our models is that we do not assume any explicit aggregative force acting on the individuals; instead, aggregation is obtained exclusively by reducing the individual stochasticity in response to higher perceived density. We formally derive the corresponding mean-field limits, leading to nonlocal degenerate diffusions. Then, we carry out the mathematical analysis of the first-order model, in particular, we prove the existence of weak solutions and show that it allows for measure-valued steady states. We also perform linear stability analysis and identify conditions for pattern formation. Moreover, we discuss the role of the nonlocality for well-posedness of the first-order model. Finally, we present results of numerical simulations for both the first- and second-order model on the individual-based and continuum levels of description.

Exponential asymptotic flocking in the Cucker-Smale model with distributed reaction delays.

We study a variant of the Cucker-Smale system with distributed reaction delays. Using backward-forward and stability estimates on the quadratic velocity fluctuations we derive sufficient conditions for asymptotic flocking of the solutions. The conditions are formulated in terms of moments of the delay distribution and they guarantee exponential decay of velocity fluctuations towards zero for large times. We demonstrate the applicability of our theory to particular delay distributions - exponential, uniform and linear. For the exponential distribution, the flocking condition can be resolved analytically, leading to an explicit formula. For the other two distributions, the satisfiability of the assumptions is investigated numerically.

Auxin transport model for leaf venation.

The plant hormone auxin controls many aspects of the development of plants. One striking dynamical feature is the self-organization of leaf venation patterns which is driven by high levels of auxin within vein cells. The auxin transport is mediated by specialized membrane-localized proteins. Many venation models have been based on polarly localized efflux-mediator proteins of the PIN family. Here, we investigate a modelling framework for auxin transport with a positive feedback between auxin fluxes and transport capacities that are not necessarily polar, i.e. directional across a cell wall. Our approach is derived from a discrete graph-based model for biological transportation networks, where cells are represented by graph nodes and intercellular membranes by edges. The edges are not a priori oriented and the direction of auxin flow is determined by its concentration gradient along the edge. We prove global existence of solutions to the model and the validity of Murray's Law for its steady states. Moreover, we demonstrate with numerical simulations that the model is able connect an auxin source-sink pair with a mid-vein and that it can also produce branching vein patterns. A significant innovative aspect of our approach is that it allows the passage to a formal macroscopic limit which can be extended to include network growth. We perform mathematical analysis of the macroscopic formulation, showing the global existence of weak solutions for an appropriate parameter range.