Density-dependent vital rates and their population dynamic consequences.

We explore a set of simple, nonlinear, two-stage models that allow us to compare the effects of density dependence on population dynamics among different kinds of life cycles. We characterize the behavior of these models in terms of their equilibria, bifurcations. and nonlinear dynamics, for a wide range of parameters. Our analyses lead to several generalizations about the effects of life history and density dependence on population dynamics. Among these are: (1) iteroparous life histories are more likely to be stable than semelparous life histories; (2) an increase in juvenile survivorship tends to be stabilizing; (3) density-dependent adult survival cannot control population growth when reproductive output is high: (4) density-dependent reproduction is more likely to cause chaotic dynamics than density dependence in other vital rates; and (5) changes in development rate have only small effects on bifurcation patterns.

Invasion speeds in fluctuating environments.

Biological invasions are increasingly frequent and have dramatic ecological and economic consequences. A key to coping with invasive species is our ability to predict their rates of spread. Traditional models of biological invasions assume that the environment is temporally constant. We examine the consequences for invasion speed of periodic and stochastic fluctuations in population growth rates and in dispersal distributions.

Body size and food web structure: testing the equiprobability assumption of the cascade model.

The cascade model successfuly predicts many patterns in reported food webs. A key assumption of this model is the existence of a predetermined trophic hierarchy; prey are always lower in the hierarchy than their predators. At least three studies have suggested that, in animal food webs, this hierarchy can be explained to a large extent by body size relationships. A second assumption of the standard cascade model is that trophic links not prohibited by the hierarchy occur with equal probability. Using nonparametric contingency table analyses, we tested this "equiprobability hypothesis" in 16 published animal food webs for which the adult body masses of the species had been estimated. We found that when the hierarchy was based on body size, the equiprobability hypothesis was rejected in favor of an alternative, "predator-dominance" hypothesis wherein the probability of a trophic link varies with the identity of the predator. Another alternative to equiprobabilty is that the probability of a trophic link depends upon the ratio of the body sizes of the two species. Using nonparametric regression and liklihood ratio tests, we show that a size-ratio based model represents a significant improvement over the cascade model. These results suggest that models with heterogeneous predation probabilities will fit food web data better than the homogeneous cascade model. They also suggest a new way to bridge the gap between static and dynamic food web models.

The subcritical collapse of predator populations in discrete-time predator-prey models.

Many discrete-time predator-prey models possess three equilibria, corresponding to (1) extinction of both species, (2) extinction of the predator and survival of the prey at its carrying capacity, or (3) coexistence of both species. For a variety of such models, the equilibrium corresponding to coexistence may lose stability via a Hopf bifurcation, in which case trajectories approach an invariant circle. Alternatively, the equilibrium may undergo a subcritical flip bifurcation with a concomitant crash in the predator's population. We review a technique for distinguishing between subcritical and supercritical flip bifurcations and provide examples of predator-prey systems with a subcritical flip bifurcation.