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

The Theory of Island Biogeography

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

Human biochemical genetics

An essential textbook for any student or researcher in biology needing to design experiments, sample programs or analyse the resulting data The text begins with a revision of estimation and hypothesis testing methods, covering both classical and Bayesian philosophies, before advancing to the analysis of linear and generalized linear models Topics covered include linear and logistic regression, simple and complex ANOVA models (for factorial, nested, block, split-plot and repeated measures and covariance designs), and log-linear models Multivariate techniques, including classification and ordination, are then introduced Special emphasis is placed on checking assumptions, exploratory data analysis and presentation of results The main analyses are illustrated with many examples from published papers and there is an extensive reference list to both the statistical and biological literature The book is supported by a website that provides all data sets, questions for each chapter and links to software

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Experimental Design and Data Analysis for Biologists

Predation has long been implicated as a major selective force in the evolution of several morphological and behavioral characteristics of animals. The importance of predation during evolutionary ti...

Behavioral decisions made under the risk of predation: a review and prospectus

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Modern Applied Statistics With S

In his recent review of the developing theory of insect-plant interactions, Gilbert (52) identified four major thrusts in research: insect-plant coevolution, host plants as islands, plant apparency and chemical defense, and resource predictability versus evolutionary strategies of insects. From his review it is evident that, with a few exceptions (23, 45, 53, 64), developing theory is addressing primarily a two trophic level system. In reality, of course, all terrestrial communities based on living plants are composed of at least three interacting trophic levels: plants, herbivores, and natural enemies of herbivores. We argue that theory on insect-plant interactions cannot progress realistically without consideration of the third trophic level. A closer look at the mechanisms of interactions reveals a paradox, and plants have many effects, direct and indirect, positive and negative, not only on herbivores but also on the enemies of herbivores. The third trophic level must be considered as part of a plant's battery of defenses against herbivores.

http://max2.ese.u-psud.fr/epc/conservation/PDFs/HIPE/Price1980.pdf

Interactions Among Three Trophic Levels: Influence of Plants on Interactions Between Insect Herbivores and Natural Enemies

Ongoing climate change has affected the ecological dynamics of many species and is expected to impose natural selection on ecologically important traits. Droughts and other anticipated changes in precipitation may be particularly potent selective factors, especially in arid regions. Here we demonstrate the evolutionary response of an annual plant, Brassica rapa, to a recent climate fluctuation resulting in a multiyear drought. Ancestral (predrought) genotypes were recovered from stored seed and raised under a set of common environments with descendant (postdrought) genotypes and with ancestordescendant hybrids. As predicted, the abbreviated growing seasons caused by drought led to the evolution of earlier onset of flowering. Descendants bloomed earlier than ancestors, advancing first flowering by 1.9 days in one study population and 8.6 days in another. The intermediate flowering time of ancestordescendant hybrids supports an additive genetic basis for divergence. Experiments confirmed that summer drought selected for early flowering, that flowering time was heritable, and that selection intensities in the field were more than sufficient to account for the observed evolutionary change. Natural selection for drought escape thus appears to have caused adaptive evolution in just a few generations. A systematic effort to collect and store propagules from suitable species would provide biologists with materials to detect and elucidate the genetic basis of further evolutionary shifts driven by climate change. contemporary evolution global climate change life history theory local adaptation plant phenology

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Rapid evolution of flowering time by an annual plant in response to a climate fluctuation.

The role of biotic interactions in shaping plant flowering phenology has long been controversial; plastic responses to the abiotic environment, limited precision of biological clocks and inconsistency of selection pressures have generally been emphasized to explain phenological variation. However, part of this variation is heritable and selection analyses show that biotic interactions can modulate selection on flowering phenology. Our review of the literature indicates that pollinators tend to favour peak or earlier flowering, whereas pre-dispersal seed predators tend to favour off-peak or later flowering. However, effects strongly vary among study systems. To understand such variation, future studies should address the impact of mutualist and antagonist dispersal ability, ecological specialization, and habitat and plant population characteristics. Here, we outline future directions to study how such interactions shape flowering phenology.

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Time after time: flowering phenology and biotic interactions

This work presents the results of over 25 years of studying plant-insect interactions. The study centres on the ecology and evolution of interactions among a host plant, the parasitic insect that attacks it, and the insects and birds that are the parasite's natural enemies. Since this system provides a model that can be subjected to experimental manipulations, it has allowed the authors to address specific theories and concepts that have guided biological research for more than two decades and to engage general problems in evolutionary biology. The specific subjects of research are the host plant goldenrod ("Solidago"), the parasitic insect "Eurosta solidaginis" ("Diptera: Tephritidae") that induces a gall on the plant stem, and a number of natural enemies of the gallfly. By presenting their detailed empirical studies of the "Solidago-Eurosta" natural enemy system, the authors demonstrate the complexities of specialized enemy-victim interactions and, thereby, the complex interactive relationships among species more broadly.

Evolutionary Ecology across Three Trophic Levels: Goldenrods, Gallmakers, and Natural Enemies

Flower-feeding insects may reduce the reproductive success of their host plant in subtle ways that go beyond a direct reduction in gametes. Pollinators may respond to floral damage by visiting damaged plants at lower rates. Fewer visitations to the plant may result in fewer flowers that receive pollinator service and as a consequence lead to lower male and/or female reproductive success. In a two-year study, we examined the direct effect of flower predation by Meligethes rufimanus on the floral display of Isomeris arborea, and the indirect effect of herbivory on pollinator behavior. Plants exposed to herbivore attack produced fewer functional inflorescences than plants protected from herbivory. Undamaged flowers produced three times as much nectar per flower as damaged flowers. Likewise, protected plants had over twice as many anthers per flower as exposed plants. Pollinators responded by visiting damaged flowers less, and exposed plants had lower flower visitation rates than protected plants. Pollinators also visited patches of protected plants more frequently than exposed patches. These results show that floral herbivory reduces pollinator service and thus may reduce reproductive success indirectly, as well as through the direct consumption of viable gametes.

Arthur E. Weis

Papers

Interactions Among Three Trophic Levels: Influence of Plants on Interactions Between Insect Herbivores and Natural Enemies

Rapid evolution of flowering time by an annual plant in response to a climate fluctuation.

Time after time: flowering phenology and biotic interactions

Evolutionary Ecology across Three Trophic Levels: Goldenrods, Gallmakers, and Natural Enemies

The consequences of floral herbivory for pollinator service to isomeris arborea