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

An informational cascade occurs when it is optimal for an individual, having observed the actions of those ahead of him, to follow the behavior of the preceding individual without regard to his own information. We argue that localized conformity of behavior and the fragility of mass behaviors can be explained by informational cascades.

https://papers.ssrn.com/sol3/Delivery.cfm/SSRN_ID1405027_code2024.pdf?abstractid=1286306&mirid=1&type=2

A Theory of Fads, Fashion, Custom, and Cultural Change as Informational Cascades

/pdf/a-theory-of-fads-fashion-custom-and-cultural-change-as-3s4j8rv8xm.pdf

Mating systems, philopatry and dispersal in birds and mammals

Beginning with Emlen (1966) and MacArthur and Pianka (1966) and extending through the last ten years, several authors have sought to predict the foraging behavior of animals by means of mathematical models. These models are very similar,in that they all assume that the fitness of a foraging animal is a function of the efficiency of foraging measured in terms of some "currency" (Schoener, 1971) -usually energy- and that natural selection has resulted in animals that forage so as to maximize this fitness. As a result of these similarities, the models have become known as "optimal foraging models"; and the theory that embodies them, "optimal foraging theory." The situations to which optimal foraging theory has been applied, with the exception of a few recent studies, can be divided into the following four categories: (1) choice by an animal of which food types to eat (i.e., optimal diet); (2) choice of which patch type to feed in (i.e., optimal patch choice); (3) optimal allocation of time to different patches; and (4) optimal patterns and speed of movements. In this review we discuss each of these categories separately, dealing with both the theoretical developments and the data that permit tests of the predictions. The review is selective in the sense that we emphasize studies that either develop testable predictions or that attempt to test predictions in a precise quantitative manner. We also discuss what we see to be some of the future developments in the area of optimal foraging theory and how this theory can be related to other areas of biology. Our general conclusion is that the simple models so far formulated are supported are supported reasonably well by available data and that we are optimistic about the value both now and in the future of optimal foraging theory. We argue, however, that these simple models will requre much modification, espicially to deal with situations that either cannot easily be put into one or another of the above four categories or entail currencies more complicated that just energy.

Citation classic - optimal foraging - a selective review of theory and tests

Part 1 Production, transmission, and reception of signals: the properties of sound fourier analysis sound production sound propogation sound reception properties of light production and transmission of light signals light signal reception chemical signals electroreception. Part 2 Optimizing information transfer: optimizing communication the amount of information the value of information coding signal evolution costs and constraints on signal evolution signal design rules. Part 3 Game theory and signalling strategies: evolutionary game theory signal honesty conflict resolution territorial signalling games mating games and signalling social integration environmental signals autocommunication.

Principles of Animal Communication

A model for the evolution of despotic versus egalitarian societies

Principles of animal communication, 2nd ed.

1.

Graphical methods are presented for the simultaneous comparisons of group size and territory size (subsumed jointly under the term “social dispersion”), in organisms with exclusive but contiguous territories. The methods are applied to recently published data on five species of neotropical emballonurid bats with particular emphasis on identifying the factors which set maximal limits on group size. The available evidence suggests that population densities, group territory sizes, and group sizes are all limited by components of the food distribution. More particularly, it is argued that minimization of annual foraging ranges is of advantage to these bats and leads to a colony territory size containing one and only one active food site at any given time. Territory size is thus determined by the average distance between successively available food sites, the number of such sites needed per year, and the average size of these sites. Maximal group size is then determined as a result of this territory size minimization and equals average richness of currently used food patches.




2.

The model predicts that where food patches are low in richness and close together, social dispersion will be fine-grained; where patches are high in richness and occur far apart, social dispersion will be coarse-grained. Since sites in this study which have many small patches tend to be located in the more stable habitats, the model also predicts that temporal stability in group size and unimodal frequency distributions of group size over space will be associated with fine-grained dispersions. The reverse is predicted for coarse-grained social dispersions.




3.

The model only predicts the maximal size colonies can take. Among the many possible factors promoting social aggregation up to the predicted maxima, only a few account for the observed congruence in colony sizes and compositions at the roost and on the foraging grounds. These include information transfer about new food sites, location of roosts centrally to reduce energy costs of transit (Horn, 1968), and stabilization of competition with conspecifics at food sites.

Sandra L. Vehrencamp

Papers

Principles of Animal Communication

A model for the evolution of despotic versus egalitarian societies

Principles of animal communication, 2nd ed.

Social organization and foraging in emballonurid bats

The energetic cost of display in male sage grouse