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Animal Species and Evolution

Belknap of Harvard University Press (1963)

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  1. Carlquist revisited: history, success, and applicability of a natural history model.Stephen R. Midway & Anne-Marie C. Hodge - 2012 - Biology and Philosophy 27 (4):497-520.
    In 1966, island biogeographer Sherwin Carlquist published a list of 24 principles governing long-distance dispersal and evolution on islands. The 24 principles describe many aspects of island biology, from long-distance dispersal and establishment to community change and assemblage. Although this was an active period for island biogeography, other models and research garnered much more attention than did Carlquist’s. In this review, over 40 years of support for or against Carlquist’s principles is presented. Recent work has supported most of the 24 (...)
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  • Positive heuristics in evolutionary biology.Richard E. Michod - 1981 - British Journal for the Philosophy of Science 32 (1):1-36.
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  • Biological Species: Natural Kinds, Individuals, or What?Ruse Michael - 1987 - British Journal for the Philosophy of Science 38 (2):225-242.
    What are biological species? Aristotelians and Lockeans agree that they are natural kinds; but, evolutionary theory shows that neither traditional philosophical approach is truly adequate. Recently, Michael Ghiselin and David Hull have argued that species are individuals. This claim is shown to be against the spirit of much modern biology. It is concluded that species are natural kinds of a sort, and that any 'objectivity' they possess comes from their being at the focus of a consilience of inductions.
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  • Towards a unified science of cultural evolution.Alex Mesoudi, Andrew Whiten & Kevin N. Laland - 2006 - Behavioral and Brain Sciences 29 (4):329-347.
    We suggest that human culture exhibits key Darwinian evolutionary properties, and argue that the structure of a science of cultural evolution should share fundamental features with the structure of the science of biological evolution. This latter claim is tested by outlining the methods and approaches employed by the principal subdisciplines of evolutionary biology and assessing whether there is an existing or potential corresponding approach to the study of cultural evolution. Existing approaches within anthropology and archaeology demonstrate a good match with (...)
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  • Inbreeding, cousin marriage, and social solidarity.Umberto Melotti - 1983 - Behavioral and Brain Sciences 6 (1):112-113.
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  • A psychologist's perspective on incest avoidance behavior.Karin C. Meiselman - 1983 - Behavioral and Brain Sciences 6 (1):112-112.
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  • Song dialects: What has to be explained, and with what?Peter K. McGregor - 1985 - Behavioral and Brain Sciences 8 (1):110-110.
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  • Straining the word “optimal”.James E. Mazur - 1991 - Behavioral and Brain Sciences 14 (2):227-227.
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  • The why and how of species.Ernst Mayr - 1988 - Biology and Philosophy 3 (4):431-441.
    The biological species concept deals both with the meaning of the sexual species as a harmonious gene pool and with its protection against deleterious outbreeding (effected by isolating mechanisms). According to the Darwin-Muller-Mayr theory isolating mechanisms are acquired by incipient species during alloparty. Isolating mechanisms are not the result of ad hoc selection, but of a change of function of properties acquired during the preceding isolation of the incipient species. The role of behavioral properties (recognition) among the isolating mechanisms has (...)
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  • The recent historiography of genetics.Ernst Mayr - 1973 - Journal of the History of Biology 6 (1):125-154.
    It is evident how much Olby and Provine have contributed to a better understanding of the emergence of genetics. It is equally evident, I believe, how many obscure issues still remain to be elucidated. Indeed, their volumes have raised as many new questions as they have answered old ones. In particular, the role of constructive as well as retarding contemporary concepts in the development of new generalizations still requires far more analysis. The somewhat independent trends of various national schools and (...)
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  • Illiger and the biological species concept.Ernst Mayr - 1968 - Journal of the History of Biology 1 (2):163-178.
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  • Answers to these comments.Ernst Mayr - 1987 - Biology and Philosophy 2 (2):212-225.
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  • How to use fitness landscape models for the analysis of collective decision-making: a case of theory-transfer and its limitations.Peter Marks, Lasse Gerrits & Johannes Marx - 2019 - Biology and Philosophy 34 (1):7.
    There is considerable correspondence between theories and models used in biology and the social sciences. One type of model that is in use in both biology and the social sciences is the fitness landscape model. The properties of the fitness landscape model have been applied rather freely in the social domain. This is partly due to the versatility of the model, but it is also due to the difficulties of transferring a model to another domain. We will demonstrate that in (...)
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  • 'Fitness' and some explanatory patterns in biology.Edward Manier - 1969 - Synthese 20 (2):206 - 218.
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  • Why was Darwin’s view of species rejected by twentieth century biologists?James Mallet - 2010 - Biology and Philosophy 25 (4):497-527.
    Historians and philosophers of science agree that Darwin had an understanding of species which led to a workable theory of their origins. To Darwin species did not differ essentially from ‘varieties’ within species, but were distinguishable in that they had developed gaps in formerly continuous morphological variation. Similar ideas can be defended today after updating them with modern population genetics. Why then, in the 1930s and 1940s, did Dobzhansky, Mayr and others argue that Darwin failed to understand species and speciation? (...)
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  • How reticulated are species?James Mallet, Nora Besansky & Matthew W. Hahn - 2016 - Bioessays 38 (2):140-149.
    Many groups of closely related species have reticulate phylogenies. Recent genomic analyses are showing this in many insects and vertebrates, as well as in microbes and plants. In microbes, lateral gene transfer is the dominant process that spoils strictly tree‐like phylogenies, but in multicellular eukaryotes hybridization and introgression among related species is probably more important. Because many species, including the ancestors of ancient major lineages, seem to evolve rapidly in adaptive radiations, some sexual compatibility may exist among them. Introgression and (...)
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  • A fourth approach to the study of learning: Are “processes” really necessary?John C. Malone - 1981 - Behavioral and Brain Sciences 4 (1):151-152.
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  • The incestuous mind.Charles J. Lumsden - 1983 - Behavioral and Brain Sciences 6 (1):112-112.
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  • Hysteria, race, and phlogiston. A model of ontological elimination in the human sciences.David Ludwig - 2014 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 45 (1):68-77.
    Elimination controversies are ubiquitous in philosophy and the human sciences. For example, it has been suggested that human races, hysteria, intelligence, mental disorder, propositional attitudes such as beliefs and desires, the self, and the super-ego should be eliminated from the list of respectable entities in the human sciences. I argue that eliminativist proposals are often presented in the framework of an oversimplified “phlogiston model” and suggest an alternative account that describes ontological elimination on a gradual scale between criticism of empirical (...)
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  • Disagreement in Scientific Ontologies.David Ludwig - 2013 - Journal for General Philosophy of Science / Zeitschrift für Allgemeine Wissenschaftstheorie (1):1-13.
    The aim of this article is to discuss the nature of disagreement in scientific ontologies in the light of case studies from biology and cognitive science. I argue that disagreements in scientific ontologies are usually not about purely factual issues but involve both verbal and normative aspects. Furthermore, I try to show that this partly non-factual character of disagreement in scientific ontologies does not lead to a radical deflationism but is compatible with a “normative ontological realism.” Finally, I argue that (...)
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  • Species differences and principles of learning: Informed generality.A. W. Logue - 1981 - Behavioral and Brain Sciences 4 (1):150-151.
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  • Thinking about Models in Evolutionary Theory.Elisabeth A. Lloyd - 1986 - Philosophica 37.
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  • Confirmation of ecological and evolutionary models.Elisabeth A. Lloyd - 1987 - Biology and Philosophy 2 (3):277-293.
    In this paper I distinguish various ways in which empirical claims about evolutionary and ecological models can be supported by data. I describe three basic factors bearing on confirmation of empirical claims: fit of the model to data; independent testing of various aspects of the model, and variety of evident. A brief description of the kinds of confirmation is followed by examples of each kind, drawn from a range of evolutionary and ecological theories. I conclude that the greater complexity and (...)
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  • Do humans maximize their inclusive fitness?Frank B. Livingstone - 1983 - Behavioral and Brain Sciences 6 (1):110-111.
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  • The example of psychology: Optimism, not optimality.Daniel S. Levine - 1991 - Behavioral and Brain Sciences 14 (2):225-226.
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  • Functional studies in bird song.R. E. Lemon - 1985 - Behavioral and Brain Sciences 8 (1):109-110.
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  • The Exercise–Affect–Adherence Pathway: An Evolutionary Perspective.Harold H. Lee, Jessica A. Emerson & David M. Williams - 2016 - Frontiers in Psychology 7.
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  • Why optimality is not worth arguing about.Stephen E. G. Lea - 1991 - Behavioral and Brain Sciences 14 (2):225-225.
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  • The myth of bacterial species and speciation.Jeffrey G. Lawrence & Adam C. Retchless - 2010 - Biology and Philosophy 25 (4):569-588.
    The Tree of Life hypothesis frames the evolutionary process as a series of events whereby lineages diverge from one another, thus creating the diversity of life as descendent lineages modify properties from their ancestors. This hypothesis is under scrutiny due to the strong evidence for lateral gene transfer between distantly related bacterial taxa, thereby providing extant taxa with more than one parent. As a result, one argues, the Tree of Life becomes confounded as the original branching structure is gradually superseded (...)
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  • Natural science, social science and optimality.Oleg Larichev - 1991 - Behavioral and Brain Sciences 14 (2):224-225.
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  • Sexual rivalry in human inbreeding or adaptive cooperation?Chet S. Lancaster - 1983 - Behavioral and Brain Sciences 6 (1):109-110.
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  • A case for less selfing and more outbreeding in reviewing the literature.Michael E. Lamb & Eric L. Charnov - 1983 - Behavioral and Brain Sciences 6 (1):109-109.
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  • More on how and why: a response to commentaries.Kevin N. Laland, John Odling-Smee, William Hoppitt & Tobias Uller - 2013 - Biology and Philosophy 28 (5):793-810.
    We are grateful to the commentators for taking the time to respond to our article. Too many interesting and important points have been raised for us to tackle them all in this response, and so in the below we have sought to draw out the major themes. These include problems with both the term ‘ultimate causation’ and the proximate-ultimate causation dichotomy more generally, clarification of the meaning of reciprocal causation, discussion of issues related to the nature of development and phenotypic (...)
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  • General process theory, ecology, and animal-human continuity: A cognitive perspective.Janet L. Lachman & Roy Lachman - 1981 - Behavioral and Brain Sciences 4 (1):149-150.
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  • The Biosemiotic Concept of the Species.Kalevi Kull - 2016 - Biosemiotics 9 (1):61-71.
    Any biological species of biparental organisms necessarily includes, and is fundamentally dependent on, sign processes between individuals. In this case, the natural category of the species is based on family resemblances, which is why a species is not a natural kind. We describe the mechanism that generates the family resemblance. An individual recognition window and biparental reproduction almost suffice as conditions to produce species naturally. This is due to assortativity of mating which is not based on certain individual traits, but (...)
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  • The ecological approach to learning.John Kruse & Edward Reed - 1981 - Behavioral and Brain Sciences 4 (1):148-149.
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  • Recent work on human nature: Beyond traditional essences.Maria Kronfeldner, Neil Roughley & Georg Toepfer - 2014 - Philosophy Compass 9 (9):642-652.
    Recent philosophical work on the concept of human nature disagrees on how to respond to the Darwinian challenge, according to which biological species do not have traditional essences. Three broad kinds of reactions can be distinguished: conservative intrinsic essentialism, which defends essences in the traditional sense, eliminativism, which suggests dropping the concept of human nature altogether, and constructive approaches, which argue that revisions can generate sensible concepts of human nature beyond traditional essences. The different constructive approaches pick out one or (...)
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  • Limited dispersal between dialects?: Hypotheses testable in the field.Donald E. Kroodsma - 1985 - Behavioral and Brain Sciences 8 (1):108-109.
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  • Biological adaptation: dependence or independence from environment?Jolanta Koszteyn & Piotr Lenartowicz - 1970 - Forum Philosophicum: International Journal for Philosophy 2 (1):71-102.
    Since more than hundred years the attempts to explain biological adaptations constitute the main current of evolutionary thinking. In 1901 C. LI. Morgan wrote: „The doctrine of evolution has rendered the study of adaptation of scientific importance. Before that doctrine was formulated, natural adaptations formed part of the mystery of special creation, and played a great role in natural theology through the use of the argument from 'design in nature’". The modem doctrine of biology stresses the importance of the environment (...)
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  • Species as historical individuals.Arnold G. Kluge - 1990 - Biology and Philosophy 5 (4):417-431.
    The species category is defined as thesmallest historical individual within which there is a parental pattern of ancestry and descent. The use of historical individual in this definition is consistent with the prevailing notion that speciesper se are not involved in processes — they are effects, not effectors. Reproductive isolation distinguishes biparental historical species from their parts, and it provides a basis for understanding the nature of the evidence used to discover historical individuals.
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  • Phyletic Gradualism versus Punctuated Equilibria: Why case histories do not suffice.J. C. Von Vaupel Klein - 1995 - Acta Biotheoretica 43 (3):259-278.
    Many attempts have been made at supporting either one of the allegedly complementary divergence models Phyletic Gradualism and Punctuated Equilibria by patterns found in specific fossil sequences. However, assessing each model's connection with reality via such “individual case histories” appears not to constitute a relevant approach. Instead, in order to correctly establish the possible merits of both concepts, the claims of each have to be verified against general evolutionary theory. This is being pointed out herein by analyzing cladogenesis at the (...)
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  • Explanatory coherence and empirical adequacy: The problem of abduction, and the justification of evolutionary models. [REVIEW]Scott A. Kleiner - 2003 - Biology and Philosophy 18 (4):513-527.
    Foundationalist theories of justification for science were undermined by the theory-ladeness thesis, which has affinities with coherentist epistemologies. A challenge for defenders of coherentist theories of scientific justification is to specify coherence relations relevant to science and to show how these relations make the truth of their bearers likely. Coherence relations include characteristics that pick out better explanations in the implementation of abductive arguments. Empiricist philosophers have attacked abductive reasoning by claiming that explanatory virtues are pragmatic, having no implications regarding (...)
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  • Plato on kinds of animals.David B. Kitts - 1987 - Biology and Philosophy 2 (3):315-328.
    Some biologists and philosophers of biology have seen in Plato an especially objectionable version of essentialism or topology. Although kinds of animals are mentioned in almost all of Plato's dialogues, in none of them is there an explicity stated doctrine of animal kinds. An examination of the dialogues has, moreover, failed to reveal some implicit but consistent and unambiguous view of kinds that Plato might have held.
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  • Transcending our biology: A virtue ethics interpretation of the appeal to nature in technological and environmental ethics.Nin Kirkham - 2013 - Zygon 48 (4):875-889.
    “Arguments from nature” are used, and have historically been used, in popular responses to advances in technology and to environmental issues—there is a widely shared body of ethical intuitions that nature, or perhaps human nature, sets some limits on the kinds of ends that we should seek, the kinds of things that we should do, or the kinds of lives that we should lead. Virtue ethics can provide the context for a defensible form of the argument from nature, and one (...)
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  • The need for the incorporation of phylogeny in the measurement of biological diversity, with special reference to ecosystem functioning research.Ian King - 2009 - Bioessays 31 (1):107-116.
    Defining and measuring biodiversity is an important research area in biology, with very interesting theoretical and applied aspects. Numerous definitions have been proposed, and these definitions of biodiversity influence how it is measured. From the still commonly used measure of species diversity, through higher taxon diversity, molecular measures, ecological measures and indicator taxa, these measures have as their fundamental shortcoming the lack of an explicit consideration of the evolutionary context represented by phylogenies. Attempts have been made to incorporate phylogenetic considerations (...)
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  • Natural kinds, natural history and ecology.A. Ross Kiester - 1980 - Synthese 43 (2):331 - 342.
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  • Units and passages: A view for evolutionary biology and ecology. [REVIEW]Masakado Kawata - 1987 - Biology and Philosophy 2 (4):415-434.
    Many authors, including paleobiologists, cladists and so on, adopt a nested hierarchical viewpoint to examine the relationships among different levels of biological organization. Furthermore, species are often considered to be unique entities in functioning evolutionary processes and one of the individuals forming a nested hierarchy.I have attempted to show that such a hierarchical view is inadequate in evolutionary biology. We should define units depending on what we are trying to explain. Units that play an important role in evolution and ecology (...)
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  • The Hypothesis of a Genetic Protolanguage: an Epistemological Investigation. [REVIEW]Gregory Katz - 2008 - Biosemiotics 1 (1):57-73.
    Progress in molecular biology has revealed profound relations between linguistic and genomic sciences, mainly through advances in bioinformatics. The structural symmetries between biochemical and verbal syntaxes raise the question of their origins: did they emerge independently, or did one arise from the other? Does the genetic code contain the traces of a protolanguage, a universal grammar whose gradual evolution and successive mutations progressively led to the polymorphism of natural languages? To explore this question, we review the isomorphism of the genetic (...)
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  • Ecology and learning.Alan C. Kamil - 1981 - Behavioral and Brain Sciences 4 (1):147-148.
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  • A funny thing happened on the way to comparative psychology.James W. Kalat - 1981 - Behavioral and Brain Sciences 4 (1):147-147.
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