No Arabic abstract
For any $N geq 2$, we show that there are choices of diffusion rates ${d_i}_{i=1}^N$ such that for $N$ competing species which are ecologically identical and having distinct diffusion rates, the slowest diffuser is able to competitive exclude the remainder of the species. In fact, the choices of such diffusion rates is open in the Hausdorff topology. Our result provides some evidence in the affirmative direction regarding the conjecture by Dockery et al. in cite{Dockery1998}. The main tools include Morse decomposition of the semiflow, as well as the theory of normalized principal bundle for linear parabolic equations.
We study the (hydro-)dynamics of multi-species driven by alignment. What distinguishes the different species is the protocol of their interaction with the rest of the crowd: the collective motion is described by different communication kernels, $phi_{alphabeta}$, between the crowds in species $alpha$ and $beta$. We show that flocking of the overall crowd emerges provided the communication array between species forms a connected graph. In particular, the crowd within each species need not interact with its own kind, i.e., $phi_{alphaalpha}=0$; different species which are engaged in such `game of alignment require a connecting path for propagation of information which will lead to the flocking of overall crowd. The same methodology applies to multi-species aggregation dynamics governed by first-order alignment: connectivity implies concentration around an emerging consensus.
This paper studies the traveling wave solutions to a three species competition cooperation system. The existence of the traveling waves is investigated via monotone iteration method. The upper and lower solutions come from either the waves of KPP equation or those of certain Lotka Volterra system. We also derive the asymptotics and uniqueness of the wave solutions. The results are then applied to a Lotka Volterra system with spatially averaged and temporally delayed competition.
We are concerned with the persistence of both predator and prey in a diffusive predator-prey system with a climate change effect, which is modeled by a spatial-temporal heterogeneity depending on a moving variable. Moreover, we consider both the cases of nonlocal and local dispersal. In both these situations, we first prove the existence of forced waves, which are positive stationary solutions in the moving frames of the climate change, of either front or pulse type. Then we address the persistence or extinction of the prey and the predator separately in various moving frames, and achieve a complete picture in the local diffusion case. We show that the survival of the species depends crucially on how the climate change speed compares with the minimal speed of some pulse type forced waves.
We analyze several florae (collections of plant species populating specific areas) in different geographic and climatic regions. For every list of species we produce a taxonomic classification tree and we consider its statistical properties. We find that regardless of the geographical location, the climate and the environment all species collections have universal statistical properties that we show to be also robust in time. We then compare observed data sets with simulated communities obtained by randomly sampling a large pool of species from all over the world. We find differences in the behavior of the statistical properties of the corresponding taxonomic trees. Our results suggest that it is possible to distinguish quantitatively real species assemblages from random collections and thus demonstrate the existence of correlations between species.
We study the regularity and large-time behavior of a crowd of species driven by chemo-tactic interactions. What distinguishes the different species is the way they interact with the rest of the crowd: the collective motion is driven by different chemical reactions which end up in a coupled system of parabolic Patlak-Keller-Segel equations. We show that the densities of the different species diffuse to zero provided the chemical interactions between the different species satisfy certain sub-critical condition; the latter is intimately related to a log-Hardy-Littlewood-Sobolev inequality for systems due to Shafrir & Wolansky. Thus for example, when two species interact, one of which has mass less than $4pi$, then the 2-system stays smooth for all time independent of the total mass of the system, in sharp contrast with the well-known breakdown of one specie with initial mass$> 8pi$.