Metapopulation dynamics are jointly regulated by local and spatial factors. These factors may affect the dynamics of local populations and of the entire metapopulation differently. Previous studies have shown that dispersal can stabilize local populations; however, as dispersal also tends to increase spatial synchrony, its net effect on metapopulation stability has been controversial. Here we p...

We link spatially explicit climate change predictions to a dynamic metapopulation model. Predictions of species' responses to climate change, incorporating metapopulation dynamics and elements of dispersal, allow us to explore the range margin dynamics for two lagomorphs of conservation concern. Although the lagomorphs have very different distribution patterns, shifts at the edge of the range w...

Migration is the key process to understand the dynamics and persistence of a metapopulation. Many metapopulation models assume a positive correlation between habitat patch size or stability and the number of emigrants. However, few empirical data exist, and habitat patch size and habitat stability may affect dispersal differently than they affect local persistence. Here, we studied the producti...

Metapopulation theory has recently been stirred by the development of a metapopulation persistence criterion (R(m)) quantifying the "lifetime dispersal success" of a newly colonized deme in a sparsely occupied metapopulation. No rigorous proof of this criterion in continuous time has been available so far. Here, we show that this criterion can be mathematically justified from standard Jacobian ...

Metapopulation models are widely used to study species that occupy patchily distributed habitat, but are rarely applied to migratory species, because of the difficulty of identifying demographically independent subpopulations. Here, we extend metapopulation theory to describe the directed seasonal movement of migratory populations between two sets of habitat patches, breeding and non-breeding, ...

Increasing the colonization rate of metapopulations can improve persistence, but can also increase exposure to threats. To make good decisions, managers must understand whether increased colonization is beneficial or detrimental to metapopulation persistence. While a number of studies have examined interactions between metapopulations, colonization, and threats, they have assumed that threat dy...

1. The presence/absence of a species at a particular site is the simplest form of data that can be collected during ecological field studies. We used 13 years (1990-2002) of survey data to parameterize a stochastic patch occupancy model for a metapopulation of the yellow-bellied marmot in Colorado, and investigated the significance of particular patches and the influence of site quality, networ...

Classical metapopulation theory assumes a static landscape. However, empirical evidence indicates many metapopulations are driven by habitat succession and disturbance. We develop a stochastic metapopulation model, incorporating habitat disturbance and recovery, coupled with patch colonization and extinction, to investigate the effect of habitat dynamics on persistence. We discover that habitat...

Diverse and interacting spawning groups of Atlantic herring (Clupea harengus) have varying degrees of independence to environmental conditions. How these population components respond independently to the same set of environmental conditions, and are connected through straying or entrainment, will contribute to the aggregate metapopulation dynamics. The consequences of connectivity for producti...

A metapopulation model with explicit local dynamics is studied. Unlike many patch-based metapopulation models which assume that the local population within each patch is at its equilibrium, our model incorporates population changes in local patches that interact with metapopulation dynamics. The model keeps track of the fractions of patches that have species 1 only, species 2 only, or both spec...