We consider the model of Deijfen, Häggström and Bagley (2004) for competing growth of two infection types in Rd, based on the Richardson model on Zd. Stochastic ball-shaped infection outbursts transmit the infection type of the center to all points of the ball that are not yet infected. Relevant parameters of the model are the initial infection configuration, the (type-dependent) growth rates, and the radius distribution of the infection outbursts. The main question is that of coexistence: Which values of the parameters allow the unbounded growth of both types with positive probability? Deijfen, Häggström and Bagley (2004) conjectured that the initial configuration is basically irrelevant for this question, and gave a proof for this under strong assumptions on the radius distribution, which, e.g. do not include the case of a deterministic radius. Here we give a proof that does not rely on these assumptions. One of the tools to be used is a slight generalization of the model with immune regions and delayed initial infection configurations.

We consider a stochastic model describing the growth of two competing infections on ℝd. The growth takes place by way of spherical outbursts in the infected region, an outburst in the type-1 or -2 infected region causing all previously uninfected points within a stochastic distance from the outburst location to become type-1 or -2 infected, respectively. The main result is that, if the infection types have the same intensity, then there is a strictly positive probability that both infection types grow unboundedly.

A continuum growth model is introduced. The state at time t, St, is a subset of ℝd and consists of a connected union of randomly sized Euclidean balls, which emerge from outbursts at their centre points. An outburst occurs somewhere in St after an exponentially distributed time with expected value |St|-1 and the location of the outburst is uniformly distributed over St. The main result is that, if the distribution of the radii of the outburst balls has bounded support, then St grows linearly and St/t has a nonrandom shape as t → ∞. Due to rotational invariance the asymptotic shape must be a Euclidean ball.

An interacting particle system modelling competing growth on the ℤ2 lattice is defined as follows. Each x ∈ ℤ2 is in one of the states {0,1,2}. 1's and 2's remain in their states for ever, while a 0 flips to a 1 (a 2) at a rate equal to the number of its neighbours which are in state 1 (2). This is a generalization of the well-known Richardson model. 1's and 2's may be thought of as two types of infection, and 0's as uninfected sites. We prove that if we start with a single site in state 1 and a single site in state 2, then there is positive probability for the event that both types of infection reach infinitely many sites. This result implies that the spanning tree of time-minimizing paths from the origin in first passage percolation with exponential passage times has at least two topological ends with positive probability.