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The Structure of Biological Science

New York: Cambridge University Press (1985)

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  1. ‘Innate’: Outdated and inadequate or linguistic convenience?Eugene S. Morton - 1988 - Behavioral and Brain Sciences 11 (4):642-643.
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  • Hominids, coalitions, and weapons: Not vehicles.Jim Moore - 1994 - Behavioral and Brain Sciences 17 (4):632-632.
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  • The infinite regress of optimization.Philippe Mongin - 1991 - Behavioral and Brain Sciences 14 (2):229-230.
    A comment on Paul Schoemaker's target article in Behavioral and Brain Sciences, 14 (1991), p. 205-215, "The Quest for Optimality: A Positive Heuristic of Science?" (https://doi.org/10.1017/S0140525X00066140). This comment argues that the optimizing model of decision leads to an infinite regress, once internal costs of decision (i.e., information and computation costs) are duly taken into account.
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  • Function, fitness and disposition.Sandra D. Mitchell - 1995 - Biology and Philosophy 10 (1):39-54.
    In this paper I discuss recent debates concerning etiological theories of functions. I defend an etiological theory against two criticisms, namely the ability to account for malfunction, and the problem of structural doubles. I then consider the arguments provided by Bigelow and Pargetter (1987) for a more forward looking account of functions as propensities or dispositions. I argue that their approach fails to address the explanatory problematic for which etiological theories were developed.
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  • Dimensions of scientific law.Sandra D. Mitchell - 2000 - Philosophy of Science 67 (2):242-265.
    Biological knowledge does not fit the image of science that philosophers have developed. Many argue that biology has no laws. Here I criticize standard normative accounts of law and defend an alternative, pragmatic approach. I argue that a multidimensional conceptual framework should replace the standard dichotomous law/ accident distinction in order to display important differences in the kinds of causal structure found in nature and the corresponding scientific representations of those structures. To this end I explore the dimensions of stability, (...)
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  • Two dynamic criteria for validating claims of optimality.Geoffrey F. Miller - 1991 - Behavioral and Brain Sciences 14 (2):228-229.
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  • Complexity and optimality.Dauglas A. Miller & Steven W. Zucker - 1991 - Behavioral and Brain Sciences 14 (2):227-228.
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  • Beyond shared fate: Group-selected mechanisms for cooperation and competition in fuzzy, fluid vehicles.Geoffrey F. Miller - 1994 - Behavioral and Brain Sciences 17 (4):630-631.
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  • Beyond interactionism: A transactional approach to behavioral development.David B. Miller - 1988 - Behavioral and Brain Sciences 11 (4):641-642.
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  • Physicalism and downward causation in psychology and the special sciences.Theo C. Meyering - 2000 - Inquiry: An Interdisciplinary Journal of Philosophy 43 (2):181-202.
    Physicalism ? or roughly the view that the stuff that physics talks about is all the stuff there is ? has had a popular press in philosophical circles during the twentieth century. And yet, at the same time, it has become quite fashionable lately to believe that the mind matters in this world after all and that psychology is an autonomous science irreducible to physics. However, if (true, downward) mental causation implies non-reducibility and Physicalism implies the converse, it is hard (...)
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  • Formulating physicalism: Two suggestions.Andrew Melnyk - 1995 - Synthese 105 (3):381-407.
    Two ways are considered of formulating a version of retentive physicalism, the view that in some important sense everything is physical, even though there do exist properties, e.g. higher-level scientific ones, which cannot be type-identified with physical properties. The first way makes use of disjunction, but is rejected on the grounds that the results yield claims that are either false or insufficiently materialist. The second way, realisation physicalism, appeals to the correlative notions of a functional property and its realisation, and (...)
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  • Gould on laws in biological science.Lee Mcintyre - 1997 - Biology and Philosophy 12 (3):357-367.
    Are there laws in evolutionary biology? Stephen J. Gould has argued that there are factors unique to biological theorizing which prevent the formulation of laws in biology, in contradistinction to the case in physics and chemistry. Gould offers the problem of complexity as just such a fundamental barrier to biological laws in general, and to Dollos Law in particular. But I argue that Gould fails to demonstrate: (1) that Dollos Law is not law-like, (2) that the alleged failure of Dollos (...)
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  • Straining the word “optimal”.James E. Mazur - 1991 - Behavioral and Brain Sciences 14 (2):227-227.
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  • Answers to these comments.Ernst Mayr - 1987 - Biology and Philosophy 2 (2):212-225.
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  • Proper functions and aristotelian functions in biology.Barry Maund - 2000 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 31 (1):155-178.
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  • Proper functions and Aristotelian functions in biology.Barry Maund - 2000 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 31 (1):155-178.
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  • Análisis de la teoría genética a la luz de la estructura de las revoluciones científicas.Pedro Martínez-Gómez, Ana Cuevas-Badallo & María Cerezo - 2015 - Revista de Humanidades de Valparaíso 6:29-48.
    The Post-genomic Era includes features both from a methodological and epistemic point of view and from an ontological perspective. Firstly, it incorporates new methods of high-throughput sequencing of DNA and RNA, and the development of complete genomes that allow a precise reference of the molecular results obtained. In addition, from an ontological perspective, the centre of gravity of the molecular processes is placed on the expression of genes, and the way in which such expression is regulated; these features turn the (...)
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  • Group evolutionary strategies: Dimensions and mechanisms.Kevin MacDonald - 1994 - Behavioral and Brain Sciences 17 (4):629-630.
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  • The awakened brain: From Wright's psychozoology to Barkow's selfless persons.David Paul Lumsden - 1991 - Behavioral and Brain Sciences 14 (2):311-312.
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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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  • 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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  • Rx: Distinguish group selection from group adaptation.Elisabeth A. Lloyd - 1994 - Behavioral and Brain Sciences 17 (4):628-629.
    I admire Wilson & Sober's (W & S's) aim, to alert social scientists that group selection has risen from the ashqs, and to explicate its relevance to the behavioral sciences. Group selection has beenwidely misunderstood; furthermore, both authors have been instrumental in illuminating conceptual problems surrounding higher-level selection. Still, I find that this target article muddies the waters, primarily through its shifting and confused definition of a "vehicle" of selection. The fundamental problem is an ambiguity in the definition of "adaptation." (...)
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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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  • Birdsong development: Real or imagined results?R. E. Lemon - 1988 - Behavioral and Brain Sciences 11 (4):640-641.
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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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  • Natural science, social science and optimality.Oleg Larichev - 1991 - Behavioral and Brain Sciences 14 (2):224-225.
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  • Explanation, causation, and evolution.Jean Lachapelle - 1997 - Biology and Philosophy 12 (2):243-257.
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  • Reviews. [REVIEW]Bruce Kuklick - 1987 - British Journal for the Philosophy of Science 38 (1):117-119.
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  • Song development and sexual imprinting: Toward an interactionist approach.Jaap P. Kruijt & Carel ten Cate - 1988 - Behavioral and Brain Sciences 11 (4):640-640.
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  • Behavioral ontogeny research: No pain, no gain?Donald E. Kroodsma - 1988 - Behavioral and Brain Sciences 11 (4):639-640.
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  • Multiple Realizability as a design heuristic in biological engineering.Rami Koskinen - 2018 - European Journal for Philosophy of Science 9 (1):15.
    Recently, several critics of the multiple realizability thesis have argued that philosophers have tended to accept the thesis on too weak grounds. On the one hand, the analytic challenge has problematized how philosophers have treated the multiple realization relation itself, claiming that assessment of the sameness of function and the relevant difference of realizers has been uncritical. On the other hand, it is argued that the purported evidence of the thesis is often left empirically unverified. This paper provides a novel (...)
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  • Biological hierarchies, their birth, death and evolution by natural selection.Robert W. Korn - 2002 - Biology and Philosophy 17 (2):199-221.
    Description of the biologicalhierarchy of the organism has been extendedhere to included the evolutionary andecological sub-hierarchies with theirrespective levels in order to give a completehierarchical description of life. These newdescriptions include direction of formation,types of constraints, and dual levels. Constraints are produced at the macromolecularlevel of genes/proteins, some of which (a) aredescendent restraints which hold a hierarchytogether and others (b) interact horizontallywith selective agents at corresponding levelsof the niche. The organism is a dual levelconstrained by both the ecologicalsub-hierarchy (survival) and (...)
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  • When is developmental biology not developmental biology?Ronald Konopka - 1988 - Behavioral and Brain Sciences 11 (4):639-639.
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  • Lowe's argument for dualism from mental causation.Max Kistler - 2005 - Philosophia 33 (1-4):319-329.
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  • Supervenience and explanation.Harold Kincaid - 1988 - Synthese 77 (November):251-81.
    This paper explores the explanatory adequacy of lower-level theories when their higher-level counterparts are irreducible. If some state or entity described by a high-level theory supervenes upon and is realized in events, entities, etc. described by the relevant lower-level theory, does the latter fully explain the higher-level event even if the higher-level theory is irreducible? While the autonomy of the special sciences and the success of various eliminativist programs depends in large part on how we answer this question, neither the (...)
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  • Ducks don't sing.Andrew P. King & Meredith J. West - 1988 - Behavioral and Brain Sciences 11 (4):638-639.
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  • Ab ovo with song?S. N. Khayutin & L. I. Alexandrov - 1988 - Behavioral and Brain Sciences 11 (4):637-638.
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  • Normativity in the Philosophy of Science.Marie I. Kaiser - 2019 - Metaphilosophy 50 (1-2):36-62.
    This paper analyzes what it means for philosophy of science to be normative. It argues that normativity is a multifaceted phenomenon rather than a general feature that a philosophical theory either has or lacks. It analyzes the normativity of philosophy of science by articulating three ways in which a philosophical theory can be normative. Methodological normativity arises from normative assumptions that philosophers make when they select, interpret, evaluate, and mutually adjust relevant empirical information, on which they base their philosophical theories. (...)
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  • Developmental explanation and the ontogeny of birdsong: Nature/nurture redux.Timothy Johnston - 1988 - Behavioral and Brain Sciences 11 (4):617-630.
    Despite several decades of criticism, dichotomous thinking about behavioral development remains widespread and influential. This is particularly true in study of birdsong development, where it has become increasingly common to diagnose songs, elements of songs, or precursors of songs as either innate or learned on the basis of isolation-rearing experiments. The theory of sensory templates has encouraged both the dichotomous approach and an emphasis on structural rather than functional aspects of song development. As a result, potentially important lines of investigation (...)
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  • Challenges to an interactionist approach to the study of song development.Timothy D. Johnston - 1988 - Behavioral and Brain Sciences 11 (4):651-663.
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  • On the Definition of Life.L. I. Jianhui - 2019 - Philosophy Study 9 (9).
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  • The polythetic perspective.Donald D. Jensen - 1988 - Behavioral and Brain Sciences 11 (4):637-637.
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  • Types of optimality: Who is the steersman?Michael E. Hyland - 1991 - Behavioral and Brain Sciences 14 (2):223-224.
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  • Different vehicles for group selection in humans.Michael E. Hyland - 1994 - Behavioral and Brain Sciences 17 (4):628-628.
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  • Taking vechicles seriously.David L. Hull - 1994 - Behavioral and Brain Sciences 17 (4):627-628.
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  • An evolutionary account of science: A response to Rosenberg's critical notice. [REVIEW]David L. Hull - 1992 - Biology and Philosophy 7 (2):229-236.
    In his critical notice, Rosenberg (1991) raises three objections to my evolutionary account of science: whether it is more than a week metaphor, the compatibility of my past objections to reduction and my current advocacy of viewing selection in terms of replication and interaction, and finally, the feasibility of identifying appropriate replicators and interactors in biological evolution, let alone conceptual evolution. I discuss each of these objections in turn.
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  • Person schemas: Evolutionary, individual developmental and social sources.Mardi J. Horowitz - 1991 - Behavioral and Brain Sciences 14 (2):309-310.
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  • Selective breeding–selective rearing interactions and the ontogeny of aggressive behavior.Kathryn E. Hood - 1988 - Behavioral and Brain Sciences 11 (4):636-636.
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  • Groups as vehicles and replicators: The problem of group-level adaptation.Kent E. Holsinger - 1994 - Behavioral and Brain Sciences 17 (4):626-627.
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  • Empirically equivalent theories.Harmon R. Holcomb - 1994 - Behavioral and Brain Sciences 17 (4):625-626.
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