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  1. Methodological problems in evolutionary biology I. Testability and tautologies.Wim J. Van Der Steen - 1983 - Acta Biotheoretica 32 (3):207-215.
    The impact of philosophy of science on biology is slight. Evolutionary biology, however, is nowadays an exception. The status of the neo-Darwinian theory of evolution is seriously challenged from a methodological perspective. However, the methodology used in the relevant discussions is plainly defective. A correct application of methodology to evolutionary theory leads to the following conclusions. The theory of natural selection is unfalsifiable in a strict sense of the term. This, however, does not militate against the theory, because no scientific (...)
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  • Each behavior is a product of heredity and experience.Douglas Wahlsten - 1984 - Behavioral and Brain Sciences 7 (4):699-700.
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  • (1 other version)Probabilistic causation and the explanatory role of natural selection.Pablo Razeto-Barry & Ramiro Frick - 2011 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 42 (3):344-355.
    The explanatory role of natural selection is one of the long-term debates in evolutionary biology. Nevertheless, the consensus has been slippery because conceptual confusions and the absence of a unified, formal causal model that integrates different explanatory scopes of natural selection. In this study we attempt to examine two questions: (i) What can the theory of natural selection explain? and (ii) Is there a causal or explanatory model that integrates all natural selection explananda? For the first question, we argue that (...)
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  • (1 other version)Probabilistic causation and the explanatory role of natural selection.Pablo Razeto-Barry & Ramiro Frick - 2011 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 42 (3):344-355.
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  • The emerging structure of the Extended Evolutionary Synthesis: where does Evo-Devo fit in?Alejandro Fábregas-Tejeda & Francisco Vergara-Silva - 2018 - Theory in Biosciences 137.
    The Extended Evolutionary Synthesis (EES) debate is gaining ground in contemporary evolutionary biology. In parallel, a number of philosophical standpoints have emerged in an attempt to clarify what exactly is represented by the EES. For Massimo Pigliucci, we are in the wake of the newest instantiation of a persisting Kuhnian paradigm; in contrast, Telmo Pievani has contended that the transition to an EES could be best represented as a progressive reformation of a prior Lakatosian scientific research program, with the extension (...)
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  • The idea of rationality and its relationship to social science: Comments on Popper's philosophy of the social sciences.Michael Schmid - 1988 - Inquiry: An Interdisciplinary Journal of Philosophy 31 (4):451 – 469.
    Popper has proposed a ?theory of situational rationality? as a basis for the social sciences. This theory of rational action is reconstructed and its methodological and substantial implications discussed. It is shown that methodologically Popper's idea of rational action leads to a version of theoretical instrumentalism which is incompatible with his general philosophy of science, and that substantially it implies an unacceptable theory of social institutions. Instrumentalism can be avoided by a more contentful theory of human action encompassing ?non?rational? or (...)
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  • Bas Van Fraassen y la Ley de Hardy-Weinberg: una discusión y desarrolo de su diagnóstico.Pablo Lorenzano - 2008 - Principia: An International Journal of Epistemology 12 (2):121-154.
    The aim of this article is to discuss and develop the diagnose of the Hardy-Weinberg law made by van Fraassen (1987, p. 110), according to which: 1) that law cannot be considered a law used as an axiom for the classical population genetics as a whole, since it is an equilibrium-law that holds only under certain special conditions; 2) it just determines a subclass of models; 3) its generalization shades off into logical vacuity; and 4) more complex variants of the (...)
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  • The phylogeny and ontogeny of behavior.B. F. Skinner - 1984 - Behavioral and Brain Sciences 7 (4):669-677.
    Responses are strengthened by consequences having to do with the survival of individuals and species. With respect to the provenance of behavior, we know more about ontogenic than phylogenic contingencies. The contingencies responsible for unlearned behavior acted long ago. This remoteness affects our scientific methods, both experimental and conceptual. Until we have identified he variables responsible for an event, we tend to invent causes. Explanatory entities such as “instincts,” “drives,” and “traits” still survive. Unable to show how organisms can behave (...)
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  • Theories, systemic models (SYMOs), laws and facts in the sciences.G. D. Wassermann - 1989 - Synthese 79 (3):489 - 514.
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  • Evolutionary synthesis: A search for the strategy.Juha Tuomi - 1992 - Philosophy of Science 59 (3):429-438.
    The goal of evolutionary theory is to (a) specify the general causal structure of evolving systems and (b) analyze evolutionary consequences that are expected to result from the proposed structure of the model systems. Biologists frequently emphasize the hypothetico-deductive method in evolutionary theory. I will show that this method primarily provides a tactical device for (b), while evolutionary synthesis requires a foundation of a unifying conceptual model for (a). Therefore, any successful strategy for a new synthesis requires both a new (...)
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  • The ecological approach revisited.Timothy D. Johnson - 1983 - Behavioral and Brain Sciences 6 (1):184-187.
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  • The structure versus the provenance of behavior.Jerry A. Hogan - 1984 - Behavioral and Brain Sciences 7 (4):690-690.
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  • Is evolution of behavior operant conditioning writ large?Anatol Rapoport - 1984 - Behavioral and Brain Sciences 7 (4):696-696.
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  • Skinner's blind eye.H. J. Eysenck - 1984 - Behavioral and Brain Sciences 7 (4):686-687.
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  • Lingering Haeckelian influences and certain other inadequacies of the operant viewpoint for phylogeny and ontogeny.Gilbert Gottlieb - 1984 - Behavioral and Brain Sciences 7 (4):688-689.
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  • Ethology ignored Skinner to its detriment.Jack P. Hailman - 1984 - Behavioral and Brain Sciences 7 (4):689-690.
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  • Neuropsychology vis-à-vis Skinner's behaviouristic psychology.Gerhard D. Wassermann - 1984 - Behavioral and Brain Sciences 7 (4):700-701.
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  • Human Behaviour and Biology.G. D. Wassermann - 1983 - Dialectica 37 (3):169-184.
    SummaryExtremism in the environment‐versus innateness controversy in the behavioural sciences and in human sociobiology is being examined. Genetic effects can be severely modified or overruled by environmental factors, but may, nevertheless, be important. Dawkins' view that we are survival machines programmed to subserve selfish genes seems untenable and is a root of racialism. It is also argued that morality is compatible with mixed genetic and environmental control of brains via existing biological machinery.
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  • Ecology and learning: Some historical and analytical perspectives.Edward A. Wasserman - 1983 - Behavioral and Brain Sciences 6 (1):183-184.
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  • Reinforcement is the problem, not the solution: Variation and selection of behavior.J. E. R. Staddon - 1984 - Behavioral and Brain Sciences 7 (4):697-699.
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  • Phylogenic and ontogenic environments.B. F. Skinner - 1984 - Behavioral and Brain Sciences 7 (4):701-711.
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  • Skinner's practical metaphysic may be impractical.S. N. Salthe - 1984 - Behavioral and Brain Sciences 7 (4):696-697.
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  • Nature and nurture revisited.H. C. Plotkin - 1984 - Behavioral and Brain Sciences 7 (4):695-696.
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  • Hereditary ≠ innate.Robert Plomin & Denise Daniels - 1984 - Behavioral and Brain Sciences 7 (4):694-695.
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  • B. F. Skinner and the flaws of sociobiology.Anthony J. Perzigian - 1984 - Behavioral and Brain Sciences 7 (4):693-694.
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  • The use of evolutionary analogies and the rejection of state variables by B. F. Skinner.Alejandro Kacelnik & Alasdair Houston - 1984 - Behavioral and Brain Sciences 7 (4):691-692.
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  • Difficulties with phylogenetic and ontogenetic concepts.Irenäus Eibl-Eibesfeldt - 1984 - Behavioral and Brain Sciences 7 (4):685-686.
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  • What will we gain from an ecological approach to learning? Another ethologist's view.Helmut C. Mueller - 1983 - Behavioral and Brain Sciences 6 (1):182-183.
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  • From observation to principles of learning: A long and problematic route.Claire F. Michales & M. T. Turvey - 1983 - Behavioral and Brain Sciences 6 (1):181-182.
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  • Theory is as Theory Does: Scientific Practice and Theory Structure in Biology.Alan C. Love - 2013 - Biological Theory 7 (4):325-337, 430.
    Using the context of controversies surrounding evolutionary developmental biology (EvoDevo) and the possibility of an Extended Evolutionary Synthesis, I provide an account of theory structure as idealized theory presentations that are always incomplete (partial) and shaped by their conceptual content (material rather than formal organization). These two characteristics are salient because the goals that organize and regulate scientific practice, including the activity of using a theory, are heterogeneous. This means that the same theory can be structured differently, in part because (...)
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  • Molar concepts and mentalistic theories: A moral perspective.Stephen Kaplan - 1984 - Behavioral and Brain Sciences 7 (4):692-693.
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  • Behavior in the light of identified neurons.Graham Hoyle - 1984 - Behavioral and Brain Sciences 7 (4):690-691.
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  • B. F. Skinner versus Dr. Pangloss.Michael T. Ghiselin - 1984 - Behavioral and Brain Sciences 7 (4):687-688.
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  • Am l a closet general process learning.Bennett G. Galef - 1983 - Behavioral and Brain Sciences 6 (1):180-181.
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  • On measuring canalized behavior.Alex S. Fraser & Harold D. Fishbein - 1983 - Behavioral and Brain Sciences 6 (1):179-180.
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  • Consequence contingencies and provenance partitions.Juan D. Delius - 1984 - Behavioral and Brain Sciences 7 (4):685-685.
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  • Operant conditioning and natural selection.Andrew M. Colman - 1984 - Behavioral and Brain Sciences 7 (4):684-685.
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  • The general algorithm for adaptation in learning, evolution, and perception.Donald T. Campbell - 1983 - Behavioral and Brain Sciences 6 (1):178-179.
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  • Ethology and operant psychology.Gordon M. Burghardt - 1984 - Behavioral and Brain Sciences 7 (4):683-684.
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  • Cost–benefit models and the evolution of behavior.Jerram L. Brown - 1984 - Behavioral and Brain Sciences 7 (4):682-682.
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  • A new experimental analysis of behavior – one for all behavior.D. Caroline Blanchard, Robert J. Blanchard & Kevin J. Flannelly - 1984 - Behavioral and Brain Sciences 7 (4):681-682.
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  • Of false dichotomies and larger frames.Jerome H. Barkow - 1984 - Behavioral and Brain Sciences 7 (4):680-681.
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  • Contingencies of selection, reinforcement, and survival.David P. Barash - 1984 - Behavioral and Brain Sciences 7 (4):680-680.
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  • Ontogenetic or phylogenetic – another afterpain of the fallacious Cartesian dichotomy.Gerard P. Baerends - 1984 - Behavioral and Brain Sciences 7 (4):679-680.
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  • Skinner's circus.Stuart A. Altmann - 1984 - Behavioral and Brain Sciences 7 (4):678-679.
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