Steven C. Walker

Bio: Steven C. Walker is an academic researcher from National Research Council. The author has contributed to research in topics: Species richness & Species evenness. The author has an hindex of 17, co-authored 27 publications receiving 49210 citations. Previous affiliations of Steven C. Walker include McMaster University & Université de Montréal.

pez: phylogenetics for the environmental sciences.

Abstract: UNLABELLED pez is an R package that permits measurement, modelling and simulation of phylogenetic structure in ecological data. pez contains the first implementation of many methods in R, and aggregates existing data structures and methods into a single, coherent package. AVAILABILITY AND IMPLEMENTATION pez is released under the GPL v3 open-source license, available on the Internet from CRAN (http://cran.r-project.org). The package is under active development, and the authors welcome contributions (see http://github.com/willpearse/pez). CONTACT will.pearse@gmail.com.

Functional-diversity indices can be driven by methodological choices and species richness

Abstract: Functional diversity is an important concept in community ecology because it captures information on functional traits absent in measures of species diversity. One popular method of measuring functional diversity is the dendrogram-based method, FD. To calculate FD, a variety of methodological choices are required, and it has been debated about whether biological conclusions are sensitive to such choices. We studied the probability that conclusions regarding FD were sensitive, and that patterns in sensitivity were related to alpha and beta components of species richness. We developed a randomization procedure that iteratively calculated FD by assigning species into two assemblages and calculating the probability that the community with higher FD varied across methods. We found evidence of sensitivity in all five communities we examined, ranging from a probability of sensitivity of 0 (no sensitivity) to 0.976 (almost completely sensitive). Variations in these probabilities were driven by differences in alpha diversity between assemblages and not by beta diversity. Importantly, FD was most sensitive when it was most useful (i.e., when differences in alpha diversity were low). We demonstrate that trends in functional-diversity analyses can be largely driven by methodological choices or species richness, rather than functional trait information alone.

Bumblebees learn to forage like Bayesians.

Abstract: Bayesian foraging in patchy environments requires that foragers have information about the distribution of resources among patches (prior information), either set by natural selection or learned from past experience. We test the hypothesis that bumblebee foragers can rapidly learn prior information from past experience in two very different experimental environments. In the high‐variance environment (patches of low and high quality), stochastic optimality models predicted that finding rewards should sometimes sharply increase an optimal forager’s tendency to stay in a patch (an incremental response), whereas in the uniform environment, finding rewards should always decrease the tendency to stay (a decremental response). We use Cox regression models to show that, in a matter of hours, bees learned to match both predicted responses, resulting in a reward intake rate that averaged 80% of the predicted maximum. Following training in either environment, bees’ adaptive behavior carried over to a commo...

Empirical modelling of lake water-temperature relationships: a comparison of approaches

Abstract: 1. As a result of the role that temperature plays in many aquatic processes, good predictive models of annual maximum near-surface lake water temperature across large spatial scales are needed, particularly given concerns regarding climate change. Comparisons of suitable modelling approaches are required to determine their relative merit and suitability for providing good predictions of current conditions. We developed models predicting annual maximum near-surface lake water temperatures for lakes across Canada using four statistical approaches: multiple regression, regression tree, artificial neural networks and Bayesian multiple regression. 2. Annual maximum near-surface (from 0 to 2 m) lake water-temperature data were obtained for more than 13 000 lakes and were matched to geographic, climatic, lake morphology, physical habitat and water chemistry data. We modelled 2348 lakes and three subsets thereof encompassing different spatial scales and predictor variables to identify the relative importance of these variables at predicting lake temperature. 3. Although artificial neural networks were marginally better for three of the four data sets, multiple regression was considered to provide the best solution based on the combination of model performance and computational complexity. Climatic variables and date of sampling were the most important variables for predicting water temperature in our models. 4. Lake morphology did not play a substantial role in predicting lake temperature across any of the spatial scales. Maximum near-surface temperatures for Canadian lakes appeared to be dominated by large-scale climatic and geographic patterns, rather than lake-specific variables, such as lake morphology and water chemistry.

Fitting Linear Mixed-Effects Models Using lme4

Abstract: Maximum likelihood or restricted maximum likelihood (REML) estimates of the parameters in linear mixed-effects models can be determined using the lmer function in the lme4 package for R. As for most model-fitting functions in R, the model is described in an lmer call by a formula, in this case including both fixed- and random-effects terms. The formula and data together determine a numerical representation of the model from which the profiled deviance or the profiled REML criterion can be evaluated as a function of some of the model parameters. The appropriate criterion is optimized, using one of the constrained optimization functions in R, to provide the parameter estimates. We describe the structure of the model, the steps in evaluating the profiled deviance or REML criterion, and the structure of classes or types that represents such a model. Sufficient detail is included to allow specialization of these structures by users who wish to write functions to fit specialized linear mixed models, such as models incorporating pedigrees or smoothing splines, that are not easily expressible in the formula language used by lmer.

The Theory of Island Biogeography

Abstract: Preface to the Princeton Landmarks in Biology Edition vii Preface xi Symbols Used xiii 1. The Importance of Islands 3 2. Area and Number of Speicies 8 3. Further Explanations of the Area-Diversity Pattern 19 4. The Strategy of Colonization 68 5. Invasibility and the Variable Niche 94 6. Stepping Stones and Biotic Exchange 123 7. Evolutionary Changes Following Colonization 145 8. Prospect 181 Glossary 185 References 193 Index 201

lmerTest Package: Tests in Linear Mixed Effects Models

Abstract: One of the frequent questions by users of the mixed model function lmer of the lme4 package has been: How can I get p values for the F and t tests for objects returned by lmer? The lmerTest package extends the 'lmerMod' class of the lme4 package, by overloading the anova and summary functions by providing p values for tests for fixed effects. We have implemented the Satterthwaite's method for approximating degrees of freedom for the t and F tests. We have also implemented the construction of Type I - III ANOVA tables. Furthermore, one may also obtain the summary as well as the anova table using the Kenward-Roger approximation for denominator degrees of freedom (based on the KRmodcomp function from the pbkrtest package). Some other convenient mixed model analysis tools such as a step method, that performs backward elimination of nonsignificant effects - both random and fixed, calculation of population means and multiple comparison tests together with plot facilities are provided by the package as well.

Toward a metabolic theory of ecology

Abstract: Metabolism provides a basis for using first principles of physics, chemistry, and biology to link the biology of individual organisms to the ecology of populations, communities, and ecosystems. Metabolic rate, the rate at which organisms take up, transform, and expend energy and materials, is the most fundamental biological rate. We have developed a quantitative theory for how metabolic rate varies with body size and temperature. Metabolic theory predicts how metabolic rate, by setting the rates of resource uptake from the environment and resource allocation to survival, growth, and reproduction, controls ecological processes at all levels of organization from individuals to the biosphere. Examples include: (1) life history attributes, including devel- opment rate, mortality rate, age at maturity, life span, and population growth rate; (2) population interactions, including carrying capacity, rates of competition and predation, and patterns of species diversity; and (3) ecosystem processes, including rates of biomass production and respiration and patterns of trophic dynamics. Data compiled from the ecological literature strongly support the theoretical predictions. Even- tually, metabolic theory may provide a conceptual foundation for much of ecology, just as genetic theory provides a foundation for much of evolutionary biology.

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