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B Bolker

Publications and source records attributed to B Bolker.

6 recordsLinked to original sources

Are fluctuating asymmetry studies adequately sampled? Implications of a new model for size distribution.

Previous work on fluctuating asymmetry (FA) has highlighted its controversial relationship with environmental stress and genetic architecture. While size-based measures of FA have been assumed to have half-normal distributions within populations, studies of model developmental mechanisms have suggested other plausible distributions for FA. We investigated the distribution of FA in large empirical data sets of wing shape and wing size asymmetry from three species of insects (cotton aphid Aphis gossipyii Glover, honeybee Apis mellifera, and long-legged fly Chrysosoma crinitus). Regardless of measurement method, FA was best described by a double Pareto-lognormal (DPLN) distribution or one of its limiting functional forms. To investigate convergence of mean sample FA to the population mean at various sample sizes, we sampled repeatedly under a DPLN distribution using parameter values that best fitted our data. Sample variances are much larger, and hence, convergence is slowed considerably with univariate or multivariate size-based measures of FA in contrast to a multivariate shape-based measure of FA. We suggest that much of the past work on FA may be undersampled, and we recommend using multivariate shape-based approaches or collecting larger data sets in future studies. We also discuss the implications of the DPLN distribution for understanding the developmental mechanisms underlying FA.

Animals↗

Canonical functions for dispersal-induced synchrony.

Two processes are universally recognized for inducing spatial synchrony in abundance: dispersal and correlated environmental stochasticity. In the present study we seek the expected relationship between synchrony and distance in populations that are synchronized by density-independent dispersal. In the absence of dispersal, synchrony among populations with simple dynamics has been shown to echo the correlation in the environment. We ask what functional form we may expect between synchrony and distance when dispersal is the synchronizing agent. We formulate a continuous-space, continuous-time model that explicitly represents the time evolution of the spatial covariance as a function of spatial distance. Solving this model gives us two simple canonical functions for dispersal-induced covariance in spatially extended populations. If dispersal is rare relative to birth and death, then covariances between nearby points will follow the dispersal distance distribution. At long distances, however, the covariance tails off according to exponential or Bessel functions (depending on whether the population moves in one or two dimensions). If dispersal is common, then the covariances will follow the mixture distribution that is approximately Gaussian around the origin and with an exponential or Bessel tail. The latter mixture results regardless of the original dispersal distance distribution. There are hence two canonical functions for dispersal-induced synchrony

Animals↗

Using Moment Equations to Understand Stochastically Driven Spatial Pattern Formation in Ecological Systems

Spatial patterns in biological populations and the effect of spatial patterns on ecological interactions are central topics in mathematical ecology. Various approaches to modeling have been developed to enable us to understand spatial patterns ranging from plant distributions to plankton aggregation. We present a new approach to modeling spatial interactions by deriving approximations for the time evolution of the moments (mean and spatial covariance) of ensembles of distributions of organisms; the analysis is made possible by "moment closure," neglecting higher-order spatial structure in the population. We use the growth and competition of plants in an explicitly spatial environment as a starting point for exploring the properties of second-order moment equations and comparing them to realizations of spatial stochastic models. We find that for a wide range of effective neighborhood sizes (each plant interacting with several to dozens of neighbors), the mean-covariance model provides a useful and analytically tractable approximation to the stochastic spatial model, and combines useful features of stochastic models and traditional reaction-diffusion-like models. Copyright 1997 Academic Press. Copyright 1997 Academic Press

Journal Article↗

Space, persistence and dynamics of measles epidemics.

This paper explores the relations between persistence and dynamics in measles epidemics. Most current models, including the stochastic seasonally forced and age-structured models examined here, fail to capture simultaneously the observed dynamics and persistence characteristics of epidemics in large urban populations before vaccination. Summary measures of persistence and trienniality allow us to compare epidemics in England, New York and Copenhagen with results of non-spatial and spatial stochastic models. Spatial (metapopulation) structure allow persistence and triennial dynamics to coexist i this class of models. The spatial dynamics of measles, for which detailed spatiotemporal data are available, may serve as a useful test of ideas applicable to other epidemiological and ecological systems with an important spatial component.

Data Interpretation, Statistical↗

Chaos and complexity in measles models: a comparative numerical study.

Recurrent epidemics of measles in developed countries offer a proving ground for current theories of complicated dynamics in ecological and epidemiological systems. This paper contrasts the basic forced SEIR model for measles with a variety of more complicated and realistic models, showing that variations in seasonal forcing and age-structured mixing patterns can generate a wide range of global dynamics. The well-known chaotic dynamics of the forced SEIR model appear to be absent from more realistic models, suppressed by the buffering effect of a low-risk group of pre-school children. These results, and the variety of measles dynamics seen in real populations with different demographic and geographic patterns, point out the need for age- and spatially-structured measles models and suggest caution in the construction of models for complicated systems.

Age Factors↗