Evolution of Cooperation
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PDL As a Multi-Agent Strategy Logic
PDL as a Multi-Agent Strategy Logic ∗ Extended Abstract Jan van Eijck CWI and ILLC Science Park 123 1098 XG Amsterdam, The Netherlands [email protected] ABSTRACT The logic we propose follows a suggestion made in Van Propositional Dynamic Logic or PDL was invented as a logic Benthem [4] (in [11]) to apply the general perspective of ac- for reasoning about regular programming constructs. We tion logic to reasoning about strategies in games, and links propose a new perspective on PDL as a multi-agent strategic up to propositional dynamic logic (PDL), viewed as a gen- logic (MASL). This logic for strategic reasoning has group eral logic of action [29, 19]. Van Benthem takes individual strategies as first class citizens, and brings game logic closer strategies as basic actions and proposes to view group strate- to standard modal logic. We demonstrate that MASL can gies as intersections of individual strategies (compare also express key notions of game theory, social choice theory and [1] for this perspective). We will turn this around: we take voting theory in a natural way, we give a sound and complete the full group strategies (or: full strategy profiles) as basic, proof system for MASL, and we show that MASL encodes and construct individual strategies from these by means of coalition logic. Next, we extend the language to epistemic strategy union. multi-agent strategic logic (EMASL), we give examples of A fragment of the logic we analyze in this paper was pro- what it can express, we propose to use it for posing new posed in [10] as a logic for strategic reasoning in voting (the questions in epistemic social choice theory, and we give a cal- system in [10] does not have current strategies). -
Inclusive Fitness As a Criterion for Improvement LSE Research Online URL for This Paper: Version: Accepted Version
Inclusive fitness as a criterion for improvement LSE Research Online URL for this paper: http://eprints.lse.ac.uk/104110/ Version: Accepted Version Article: Birch, Jonathan (2019) Inclusive fitness as a criterion for improvement. Studies in History and Philosophy of Science Part C :Studies in History and Philosophy of Biological and Biomedical Sciences, 76. ISSN 1369-8486 https://doi.org/10.1016/j.shpsc.2019.101186 Reuse This article is distributed under the terms of the Creative Commons Attribution- NonCommercial-NoDerivs (CC BY-NC-ND) licence. This licence only allows you to download this work and share it with others as long as you credit the authors, but you can’t change the article in any way or use it commercially. More information and the full terms of the licence here: https://creativecommons.org/licenses/ [email protected] https://eprints.lse.ac.uk/ Inclusive Fitness as a Criterion for Improvement Jonathan Birch Department of Philosophy, Logic and Scientific Method, London School of Economics and Political Science, London, WC2A 2AE, United Kingdom. Email: [email protected] Webpage: http://personal.lse.ac.uk/birchj1 This article appears in a special issue of Studies in History & Philosophy of Biological & Biomedical Sciences on Optimality and Adaptation in Evolutionary Biology, edited by Nicola Bertoldi. 16 July 2019 1 Abstract: I distinguish two roles for a fitness concept in the context of explaining cumulative adaptive evolution: fitness as a predictor of gene frequency change, and fitness as a criterion for phenotypic improvement. Critics of inclusive fitness argue, correctly, that it is not an ideal fitness concept for the purpose of predicting gene- frequency change, since it relies on assumptions about the causal structure of social interaction that are unlikely to be exactly true in real populations, and that hold as approximations only given a specific type of weak selection. -
Sensory and Cognitive Adaptations to Social Living in Insect Societies Tom Wenseleersa,1 and Jelle S
COMMENTARY COMMENTARY Sensory and cognitive adaptations to social living in insect societies Tom Wenseleersa,1 and Jelle S. van Zwedena A key question in evolutionary biology is to explain the solitarily or form small annual colonies, depending upon causes and consequences of the so-called “major their environment (9). And one species, Lasioglossum transitions in evolution,” which resulted in the pro- marginatum, is even known to form large perennial euso- gressive evolution of cells, organisms, and animal so- cial colonies of over 400 workers (9). By comparing data cieties (1–3). Several studies, for example, have now from over 30 Halictine bees with contrasting levels of aimed to determine which suite of adaptive changes sociality, Wittwer et al. (7) now show that, as expected, occurred following the evolution of sociality in insects social sweat bee species invest more in sensorial machin- (4). In this context, a long-standing hypothesis is that ery linked to chemical communication, as measured by the evolution of the spectacular sociality seen in in- the density of their antennal sensillae, compared with sects, such as ants, bees, or wasps, should have gone species that secondarily reverted back to a solitary life- hand in hand with the evolution of more complex style. In fact, the same pattern even held for the socially chemical communication systems, to allow them to polymorphic species L. albipes if different populations coordinate their complex social behavior (5). Indeed, with contrasting levels of sociality were compared (Fig. whereas solitary insects are known to use pheromone 1, Inset). This finding suggests that the increased reliance signals mainly in the context of mate attraction and on chemical communication that comes with a social species-recognition, social insects use chemical sig- lifestyle indeed selects for fast, matching adaptations in nals in a wide variety of contexts: to communicate their sensory systems. -
Coevolution to the Edge of Chaos: Coupled Fitness Landscapes, Poised States, and Coevolutionary Avalanches
J. theor. Biol. (1991) 149, 467-505 Coevolution to the Edge of Chaos: Coupled Fitness Landscapes, Poised States, and Coevolutionary Avalanches STUART A. KAUFFMANt and SONKE JOHNSEN Department of Biochemistry and Biophysics, School of Medicine, University of Pennsylvania and Sante Fe Institute, Sante Fe, New Mexico, U.S.A. (Received on 20 April 1990, Accepted in revised form on 8 August 1990) We introduce a broadened framework to study aspects of coevolution based on the NK class of statistical models of rugged fitness landscapes. In these models the fitness contribution of each of N genes in a genotype depends epistatically on K other genes. Increasing epistatic interactions increases the rugged multipeaked character of the fitness landscape. Coevolution is thought of, at the lowest level, as a coupling of landscapes such that adaptive moves by one player deform the landscapes of its immediate partners. In these models we are able to tune the ruggedness of landscapes, how richly intercoupled any two landscapes are, and how many other players interact with each player. All these properties profoundly alter the character of the coevolutionary dynamics. In particular, these parameters govern how readily coevolving ecosystems achieve Nash equilibria, how stable to perturba- tions such equilibria are, and the sustained mean fitness of coevolving partners. In turn, this raises the possibility that an evolutionary rnetadynamics due to natural selection may sculpt landscapes and their couplings to achieve coevolutionary systems able to coadapt well. The results suggest that sustained fitness is optimized when landscape ruggedness relative to couplings between landscapes is tuned such that Nash equilibria just tenuously form across the ecosystem. -
Fitness Maximization Jonathan Birch
Fitness maximization Jonathan Birch To appear in The Routledge Handbook of Evolution & Philosophy, ed. R. Joyce. Adaptationist approaches in evolutionary ecology often take it for granted that natural selection maximizes fitness. Consider, for example, the following quotations from standard textbooks: The majority of analyses of life history evolution considered in this book are predicated on two assumptions: (1) natural selection maximizes some measure of fitness, and (2) there exist trade- offs that limit the set of possible [character] combinations. (Roff 1992: 393) The second assumption critical to behavioral ecology is that the behavior studied is adaptive, that is, that natural selection maximizes fitness within the constraints that may be acting on the animal. (Dodson et al. 1998: 204) Individuals should be designed by natural selection to maximize their fitness. This idea can be used as a basis to formulate optimality models [...]. (Davies et al. 2012: 81) Yet there is a long history of scepticism about this idea in population genetics. As A. W. F. Edwards puts it: [A] naive description of evolution [by natural selection] as a process that tends to increase fitness is misleading in general, and hill-climbing metaphors are too crude to encompass the complexities of Mendelian segregation and other biological phenomena. (Edwards 2007: 353) Is there any way to reconcile the adaptationist’s image of natural selection as an engine of optimality with the more complex image of its dynamics we get from population genetics? This has long been an important strand in the controversy surrounding adaptationism.1 Yet debate here has been hampered by a tendency to conflate various different ways of thinking about maximization and what it entails. -
What Is Inclusive Fitness Theory, and What Is It For?
This is a repository copy of What is inclusive fitness theory, and what is it for?. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/110451/ Version: Accepted Version Article: Marshall, J.A.R. orcid.org/0000-0002-1506-167X (2016) What is inclusive fitness theory, and what is it for? Current Opinion in Behavioral Sciences, 12. pp. 103-108. ISSN 2352-1546 https://doi.org/10.1016/j.cobeha.2016.09.015 Article available under the terms of the CC-BY-NC-ND licence (https://creativecommons.org/licenses/by-nc-nd/4.0/) Reuse This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs (CC BY-NC-ND) licence. This licence only allows you to download this work and share it with others as long as you credit the authors, but you can’t change the article in any way or use it commercially. More information and the full terms of the licence here: https://creativecommons.org/licenses/ Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ 1 What is inclusive fitness theory, and what is it for? 2 3 James A. R. Marshall 4 5 Department of Computer Science and Department of Animal and Plant Sciences 6 University of Sheffield 7 Regent Court 8 211 Portobello 9 Sheffield S1 4DP 10 UNITED KINGDOM 11 12 Abstract: 13 Inclusive fitness theory is a cornerstone of modern evolutionary biology, yet 14 critics contend it is not general but subject to serious limitations, and is ripe for 15 replacement, for example by multilevel selection theory. -
Norms, Repeated Games, and the Role of Law
Norms, Repeated Games, and the Role of Law Paul G. Mahoneyt & Chris William Sanchiricot TABLE OF CONTENTS Introduction ............................................................................................ 1283 I. Repeated Games, Norms, and the Third-Party Enforcement P rob lem ........................................................................................... 12 88 II. B eyond T it-for-Tat .......................................................................... 1291 A. Tit-for-Tat for More Than Two ................................................ 1291 B. The Trouble with Tit-for-Tat, However Defined ...................... 1292 1. Tw o-Player Tit-for-Tat ....................................................... 1293 2. M any-Player Tit-for-Tat ..................................................... 1294 III. An Improved Model of Third-Party Enforcement: "D ef-for-D ev". ................................................................................ 1295 A . D ef-for-D ev's Sim plicity .......................................................... 1297 B. Def-for-Dev's Credible Enforceability ..................................... 1297 C. Other Attractive Properties of Def-for-Dev .............................. 1298 IV. The Self-Contradictory Nature of Self-Enforcement ....................... 1299 A. The Counterfactual Problem ..................................................... 1300 B. Implications for the Self-Enforceability of Norms ................... 1301 C. Game-Theoretic Workarounds ................................................ -
Plasticity‐Led Evolution: a Survey of Developmental Mechanisms and Empirical Tests
DOI: 10.1111/ede.12309 PERSPECTIVE Plasticity‐led evolution: A survey of developmental mechanisms and empirical tests Nicholas A. Levis | David W. Pfennig Department of Biology, University of North Carolina, Chapel Hill, Abstract North Carolina Recent years have witnessed increased interest in evaluating whether phenotypic plasticity can precede, facilitate, and possibly even bias adaptive Correspondence “ ‐ ” Nicholas A. Levis, Department of Biology, evolution. Despite accumulating evidence for plasticity led evolution (i.e., CB#3280, University of North Carolina, “PLE”), critical gaps remain, such as: how different developmental Chapel Hill, NC 27599. mechanisms influence PLE; whether some types of traits and taxa are Email: [email protected] especially prone to experience PLE; and what studies are needed to drive the field forward. Here, we begin to address these shortcomings by first speculating about how various features of development—modularity, flexible regulation, and exploratory mechanisms—mightimpactand/orbias whether and how PLE unfolds. We then review and categorize the traits and taxa used to investigate PLE. We do so both to identify systems that may be well‐suited for studying developmental mechanisms in a PLE context and to highlight any mismatches between PLE theory and existing empirical tests of this theory. We conclude by providing additional suggestions for future research. Our overarching goal is to stimulate additional work on PLE and thereby evaluate plasticity’s role in evolution. 1 | INTRODUCTION 2011; West‐Eberhard, 2003). Under this view, novel traits start out evolutionarily as environmentally The environment has long been viewed as crucial in induced phenotypic variants. Later, they come under both selecting on phenotypes and in creating those genetic control through selection on developmental phenotypes in the first place (e.g., Baldwin, 1896, processes. -
Gene-Culture Coevolution, Group Selection, and the Evolution of Cooperation
EC_2018_A12 Gene-Culture coevolution, group selection, and the evolution of Cooperation The Evolution of Cooperation How can altruism / cooperation evolve? 1 EC_2018_A12 Levels of Selection "although a high standard of morality gives but a slight or no advantage to each individual man and his children over the other men of the same tribe (...) an advancement in the standard of morality will certainly give an immense advantage to one tribe over another.” (C. Darwin, Descent of Man, 1871) Levels of Selection Individuals (“basic” [Neo]Darwinism) Genes (“Selfish-gene” Sociobiology) Groups? Multilevel selection? Higher-level adaptations? Genetic Group Selection? “Naïve group selectionism”: The probability of survival of individual living things, or of populations, increases with the degree with which they harmoniously adjust themselves to each other and to their environment. This principle is basic to the concept of the balance of nature, orders the subject matter of ecology and evolution, underlies organismic and developmental biology, and is the foundation for all sociology. (Allee et al. 1949) “The good of the species” (Wynne-Edwards) 2 EC_2018_A12 Levels of Selection Migration, genetic drift, etc: Intergroup effects weaker than intragroup, interindividual selection. Intra x intergroup differences X Wilson DS & Wilson EO (2007) Rethinking the theoretical foundation of sociobiology Multi-level selection/ limits in kin selection theory/ “major transitions” Eusociality: Kin Selection X Individual selection + preadaptations. (communal nests) Nowak, Tarnita & Wilson, “The Evolution of Eusociality”, Nature 2010 (X Abbot et al [+100!], Nature 2011) “Major Transitions” in Evolution Maynard Smith & Szathmáry 1997 “Apart from the evolution of the genetic code, all these transitions involve the coming together of previously independent replicators, to cooperate in a higher-level assembly that reproduces as a single unit.” 3 EC_2018_A12 Natural selection & the evolution of cooperation Cooperation is needed for evolution to construct new levels of organization. -
Report Concerning Jeffrey E. Epstein's Connections to Harvard University
REPORT CONCERNING JEFFREY E. EPSTEIN’S CONNECTIONS TO HARVARD UNIVERSITY Diane E. Lopez, Harvard University Vice President and General Counsel Ara B. Gershengorn, Harvard University Attorney Martin F. Murphy, Foley Hoag LLP May 2020 1 INTRODUCTION On September 12, 2019, Harvard President Lawrence S. Bacow issued a message to the Harvard Community concerning Jeffrey E. Epstein’s relationship with Harvard. That message condemned Epstein’s crimes as “utterly abhorrent . repulsive and reprehensible” and expressed “profound[] regret” about “Harvard’s past association with him.” President Bacow’s message announced that he had asked for a review of Epstein’s donations to Harvard. In that communication, President Bacow noted that a preliminary review indicated that Harvard did not accept gifts from Epstein after his 2008 conviction, and this report confirms that as a finding. Lastly, President Bacow also noted Epstein’s appointment as a Visiting Fellow in the Department of Psychology in 2005 and asked that the review address how that appointment had come about. Following up on President Bacow’s announcement, Vice President and General Counsel Diane E. Lopez engaged outside counsel, Martin F. Murphy of Foley Hoag, to work with the Office of General Counsel to conduct the review. Ms. Lopez also issued a message to the community provid- ing two ways for individuals to come forward with information or concerns about Epstein’s ties to Harvard: anonymously through Harvard’s compliance hotline and with attribution to an email ac- count established for that purpose. Since September, we have interviewed more than 40 individu- als, including senior leaders of the University, staff in Harvard’s Office of Alumni Affairs and Development, faculty members, and others. -
The Theory of Inclusive Fitness
THE THEORY OF INCLUSIVE FITNESS David C. Queller Department of Biology, WasHington University in St. Louis EMAIL: [email protected] A review of SOCIAL EVOLUTION AND INCLUSIVE FITNESS THEORY: AN INTRODUCTION. By James A. R. Marshall. Princeton: Princeton University Press. $39.95. xvii + 195 p. Index. ISBN: 9780691161563. 2015. This is a pre-copyedit version of: Queller, D.C. The theory of inclusive fitness. Book review of "Social Evolution and Inclusive Fitness Theory: An Introduction” by J.A.R. Marshall. Quarterly Review of Biology 91:343-347. 1 W. D. Hamilton was responsible for two major innovations in the early 1960’s (Hamilton, 1964). First, He invented, formalized, and made a strong case for tHe importance of kin selection, tHe idea tHat genetic alleles will be selected in part via their effects on others who share the allele. His otHer main contribution was tHe idea of inclusive fitness, a general and intuitive way of analyzing tHis kind of selection. THougH Hamilton’s ideas Have been Hugely influential, tHere Has been no book focused on the topic of inclusive fitness theory. That gap has now been filled by James MarsHall’s “Social Evolution and Inclusive Fitness THeory”. There are various ways to approach inclusive fitness. MarsHall’s main theoretical approach appeals to me because it is one that I initiated earlier in my career (Queller, 1992), using the Price equation. MarsHall’s Chapter 3 provides a nice introduction to this equation, well worth reading in its own right because of the ever-expanding utility of the Price equation in evolutionary research. -
Lecture Notes
Chapter 12 Repeated Games In real life, most games are played within a larger context, and actions in a given situation affect not only the present situation but also the future situations that may arise. When a player acts in a given situation, he takes into account not only the implications of his actions for the current situation but also their implications for the future. If the players arepatient andthe current actionshavesignificant implications for the future, then the considerations about the future may take over. This may lead to a rich set of behavior that may seem to be irrational when one considers the current situation alone. Such ideas are captured in the repeated games, in which a "stage game" is played repeatedly. The stage game is repeated regardless of what has been played in the previous games. This chapter explores the basic ideas in the theory of repeated games and applies them in a variety of economic problems. As it turns out, it is important whether the game is repeated finitely or infinitely many times. 12.1 Finitely-repeated games Let = 0 1 be the set of all possible dates. Consider a game in which at each { } players play a "stage game" , knowing what each player has played in the past. ∈ Assume that the payoff of each player in this larger game is the sum of the payoffsthat he obtains in the stage games. Denote the larger game by . Note that a player simply cares about the sum of his payoffs at the stage games. Most importantly, at the beginning of each repetition each player recalls what each player has 199 200 CHAPTER 12.