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Theodore Garland

Bio: Theodore Garland is an academic researcher from University of California, Riverside. The author has contributed to research in topics: House mice & Population. The author has an hindex of 91, co-authored 347 publications receiving 30798 citations. Previous affiliations of Theodore Garland include University of California & University of California, Irvine.


Papers
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Journal ArticleDOI
TL;DR: In this article, the authors discuss the application of Felsenstein's (1985, Am. Nat. 125: 1n15) procedures to test for correlated evolution of continuous traits.
Abstract: We discuss and clarify several aspects of applying Felsenstein's (1985, Am. Nat. 125: 1n15) procedures to test for correlated evolution of continuous traits. This is one of several available comparative methods that maps data for phenotypic traits onto an existing phylogenetic tree (derived from independent information). Application of Felsenstein's method does not require an entirely dichotomous topology. It also does not require an assumption of gradual, clocklike character evolution, as might be modeled by Brownian motion. Almost any available information can be used to estimate branch lengths (e.g., genetic distances, divergence times estimated from the fossil record or from molecular clocks, numbers of character changes from a cladistic analysis). However, the adequacy for statistical purposes of any proposed branch lengths must be verified empirically for each phytogeny and for each character. We suggest a simple way of doing this, based on graphical analysis of plots of standardized independent contrasts versus their standard deviations (i.e., the square roots of the sums of their branch lengths). In some cases, the branch lengths and/or the values of traits being studied will require transformation. An example involving the scaling of mammalian home range area is presented. Once adequately standardized, sets of independent contrasts can be analyzed using either linear or nonlinear (multiple) regression. In all cases, however, regressions (or correlations) must be computed through the origin. We also discuss ways of correcting for body size effects and how this relates to making graphical representations of relationships of standardized independent contrasts. We close with a consideration of the types of traits that can be analyzed with independent contrasts procedures and conclude that any (continuous) trait that is inherited from ancestors is appropriate for analysis, regardless of the mechanism of inheritance (e.g., genetic or cultural).

2,174 citations

Journal ArticleDOI
TL;DR: Using empirically scaled computer simulation models of continuous traits evolving along phylogenetic trees to obtain null distributions of F statistics for ANCOVA of comparative data sets is proposed.
Abstract: Biologists often compare average phenotypes of groups of species defined cladistically or on behavioral, ecological, or physiological criteria (e.g., carnivores vs. herbivores, social vs. nonsocial species, endotherms vs. ectotherms). Hypothesis testing typically is accomplished via analysis of variance (ANOVA) or covariance (ANCOVA; often with body size as a covariate). Because of the hierarchical nature of phylogenetic descent, however, species may not represent statistically independent data points, degrees of freedom may be inflated, and significance levels derived from conventional tests cannot be trusted. As one solution to this degrees of freedom problem, we propose using empirically scaled computer simulation models of continuous traits evolving along «known» phylogenetic trees to obtain null distributions of F statistics for ANCOVA of comparative data sets

1,188 citations

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TL;DR: Focal species analyses show that some tropical forest lizards were already experiencing stressful body temperatures in summer when studied several decades ago, and simulations suggest that warming will not only further depress their physiological performance in summer, but will also enable warm-adapted, open-habitat competitors and predators to invade forests.
Abstract: Biological impacts of climate warming are predicted to increase with latitude, paralleling increases in warming. However, the magnitude of impacts depends not only on the degree of warming but also on the number of species at risk, their physiological sensitivity to warming and their options for behavioural and physiological compensation. Lizards are useful for evaluating risks of warming because their thermal biology is well studied. We conducted macrophysiological analyses of diurnal lizards from diverse latitudes plus focal species analyses of Puerto Rican Anolis and Sphaerodactyus. Although tropical lowland lizards live in environments that are warm all year, macrophysiological analyses indicate that some tropical lineages (thermoconformers that live in forests) are active at low body temperature and are intolerant of warm temperatures. Focal species analyses show that some tropical forest lizards were already experiencing stressful body temperatures in summer when studied several decades ago. Simulations suggest that warming will not only further depress their physiological performance in summer, but will also enable warm-adapted, open-habitat competitors and predators to invade forests. Forest lizards are key components of tropical ecosystems, but appear vulnerable to the cascading physiological and ecological effects of climate warming, even though rates of tropical warming may be relatively low.

806 citations

Journal ArticleDOI
TL;DR: Passengerines exhibit a lower rate of evolution in both body mass and mass‐corrected BMR; passerines also have significantly smaller body masses than their sister clade, which may justify separate, clade‐specific allometric equations for prediction of avian basal metabolic rates.
Abstract: Two phylogenetic comparative methods, independent contrasts and generalized least squares models, can be used to determine the statistical relationship between two or more traits. We show that the two approaches are functionally identical and that either can be used to make statistical inferences about values at internal nodes of a phylogenetic tree (hypothetical ancestors), to estimate relationships between characters, and to predict values for unmeasured species. Regression equations derived from independent contrasts can be placed back onto the original data space, including computation of both confidence intervals and prediction intervals for new observations. Predictions for unmeasured species (including extinct forms) can be made increasingly accurate and precise as the specificity of their placement on a phylogenetic tree increases, which can greatly increase statistical power to detect, for example, deviation of a single species from an allometric prediction. We reexamine published data ...

800 citations

Journal ArticleDOI
TL;DR: Interspecific comparison is a common approach in physiological ecology, comparative physiology, and biochemistry, and in such related fields as ', functional morphology and ethology, to identify which characteristics differ among species.
Abstract: Interspecific comparison is a common approach in physiological ecology, comparative physiology, and biochemistry, and in such related fields as ';,functional morphology and ethology (Hochachka and Somero 1984; Feder et al. 1987; Brooks and McLennan 1991; Harvey and Page1 1991). In their most basic form, comparisons are used simply to identify which characteristics differ among species. Sometimes the goal is to identify alternative physiological or biomechanical mechanisms (multiple solutions; see, e.g., Bartholomew 1987) that have achieved a similar functional endpoint (e.g., longer legs vs. faster muscles, either of which may cause higher maximal sprinting abilities), or perhaps to identify new "models" in which to study particular phenomena (see, e.g., Faraci, Kilgore, and Fedde 1984; Kellogg and Shaffer 1993). Interspecific comparisons are also used frequently to elucidate the endpoint and/or the process of evolutionary adaptation, that is, genetic changes in response to natural selection (reviews in Harvey and Page1 1991; Miles and Dunham 1993; Losos and Miles 1994). Specifically, interspecific correlations between some aspect(s) of the phenotype (e.g., low rates of evaporative water loss) and some aspect(s) of the environment (e.g., heat and aridity) are taken to indicate that past and/or present natural selection acting

672 citations


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TL;DR: Preface to the Princeton Landmarks in Biology Edition vii Preface xi Symbols used xiii 1.
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

14,171 citations

Journal Article
TL;DR: This book by a teacher of statistics (as well as a consultant for "experimenters") is a comprehensive study of the philosophical background for the statistical design of experiment.
Abstract: THE DESIGN AND ANALYSIS OF EXPERIMENTS. By Oscar Kempthorne. New York, John Wiley and Sons, Inc., 1952. 631 pp. $8.50. This book by a teacher of statistics (as well as a consultant for \"experimenters\") is a comprehensive study of the philosophical background for the statistical design of experiment. It is necessary to have some facility with algebraic notation and manipulation to be able to use the volume intelligently. The problems are presented from the theoretical point of view, without such practical examples as would be helpful for those not acquainted with mathematics. The mathematical justification for the techniques is given. As a somewhat advanced treatment of the design and analysis of experiments, this volume will be interesting and helpful for many who approach statistics theoretically as well as practically. With emphasis on the \"why,\" and with description given broadly, the author relates the subject matter to the general theory of statistics and to the general problem of experimental inference. MARGARET J. ROBERTSON

13,333 citations

Journal Article
TL;DR: For the next few weeks the course is going to be exploring a field that’s actually older than classical population genetics, although the approach it’ll be taking to it involves the use of population genetic machinery.
Abstract: So far in this course we have dealt entirely with the evolution of characters that are controlled by simple Mendelian inheritance at a single locus. There are notes on the course website about gametic disequilibrium and how allele frequencies change at two loci simultaneously, but we didn’t discuss them. In every example we’ve considered we’ve imagined that we could understand something about evolution by examining the evolution of a single gene. That’s the domain of classical population genetics. For the next few weeks we’re going to be exploring a field that’s actually older than classical population genetics, although the approach we’ll be taking to it involves the use of population genetic machinery. If you know a little about the history of evolutionary biology, you may know that after the rediscovery of Mendel’s work in 1900 there was a heated debate between the “biometricians” (e.g., Galton and Pearson) and the “Mendelians” (e.g., de Vries, Correns, Bateson, and Morgan). Biometricians asserted that the really important variation in evolution didn’t follow Mendelian rules. Height, weight, skin color, and similar traits seemed to

9,847 citations

Journal ArticleDOI
06 Jun 1986-JAMA
TL;DR: The editors have done a masterful job of weaving together the biologic, the behavioral, and the clinical sciences into a single tapestry in which everyone from the molecular biologist to the practicing psychiatrist can find and appreciate his or her own research.
Abstract: I have developed "tennis elbow" from lugging this book around the past four weeks, but it is worth the pain, the effort, and the aspirin. It is also worth the (relatively speaking) bargain price. Including appendixes, this book contains 894 pages of text. The entire panorama of the neural sciences is surveyed and examined, and it is comprehensive in its scope, from genomes to social behaviors. The editors explicitly state that the book is designed as "an introductory text for students of biology, behavior, and medicine," but it is hard to imagine any audience, interested in any fragment of neuroscience at any level of sophistication, that would not enjoy this book. The editors have done a masterful job of weaving together the biologic, the behavioral, and the clinical sciences into a single tapestry in which everyone from the molecular biologist to the practicing psychiatrist can find and appreciate his or

7,563 citations

Journal ArticleDOI
TL;DR: A new, multifunctional phylogenetics package, phytools, for the R statistical computing environment is presented, with a focus on phylogenetic tree-building in 2.1.
Abstract: Summary 1. Here, I present a new, multifunctional phylogenetics package, phytools, for the R statistical computing environment. 2. The focus of the package is on methods for phylogenetic comparative biology; however, it also includes tools for tree inference, phylogeny input/output, plotting, manipulation and several other tasks. 3. I describe and tabulate the major methods implemented in phytools, and in addition provide some demonstration of its use in the form of two illustrative examples. 4. Finally, I conclude by briefly describing an active web-log that I use to document present and future developments for phytools. I also note other web resources for phylogenetics in the R computational environment.

6,404 citations