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  1. Taxonomy is older than thinking: Epigenetic decisions.Andrew Packard - 1981 - Behavioral and Brain Sciences 4 (2):296-297.
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  • How do you transmit a template?Susan Oyama - 1988 - Behavioral and Brain Sciences 11 (4):644-645.
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  • Species as Models.Jun Otsuka - 2019 - Philosophy of Science 86 (5):1075-1086.
    This article characterizes various species concepts in terms of set-theoretic models that license biological inferences and illustrates the logical connections among different species concepts. Species in this construal are abstract models, rather than biological or even tangible entities, and relate to individual organisms via representation, rather than the membership or mereological whole/part relationship. The proposal sheds new light on vexed issues of species and situates them within broader philosophical contexts of model selection, scientific representation, and scientific realism.
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  • Units “of” selection: The end of “of”?F. J. Odling-Smee & H. C. Plotkin - 1981 - Behavioral and Brain Sciences 4 (2):295-296.
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  • Conceptual errors, different perspectives, and genetic analysis of song ontogeny.Paul C. Mundinger - 1988 - Behavioral and Brain Sciences 11 (4):643-644.
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  • ‘Innate’: Outdated and inadequate or linguistic convenience?Eugene S. Morton - 1988 - Behavioral and Brain Sciences 11 (4):642-643.
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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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  • Systems of ordering data.Ernst Mayr - 1995 - Biology and Philosophy 10 (4):419-434.
    Four ordering systems have been used most frequently in taxonomy: (1) special purpose classifications, (2) downward classifications (identification schemes), (3) upward or grouping classifications (traditional), and (4) Hennigian phylogenetic systems. The special properties of these four systems are critically evaluated. Grouping classifications and phylogenetic systems have very different objectives: the former the documentation of similarity and closeness of relationship, the latter of phylogeny. Both are legitimate ordering systems.
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  • Pheneticism reconsidered.Tim Lewens - 2012 - Biology and Philosophy 27 (2):159-177.
    The pheneticist philosophy holds that biological taxa are clusters of entities united by a form of all-things-considered resemblance. This view of taxonomy has come in for almost universal criticism from philosophers, and has received little praise from biologists, over the past 30 years or so. This article defends a modest pheneticism, understood as part of a pluralist view of taxonomy. First, phenetic approaches to taxonomy are alive and well in biological practice, especially in the areas of microbiology and botany. Second, (...)
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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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  • What does Ghiselin mean by “individual”?Joseph B. Kruskal - 1981 - Behavioral and Brain Sciences 4 (2):294-295.
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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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  • When is developmental biology not developmental biology?Ronald Konopka - 1988 - Behavioral and Brain Sciences 11 (4):639-639.
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  • The Organization of Roman Religious Beliefs.Charles King - 2003 - Classical Antiquity 22 (2):275-312.
    This study will focus on the differences in the way that Roman Paganism and Christianity organize systems of beliefs. It rejects the theory that “beliefs” have no place in the Roman religion, but stresses the differences between Christian orthodoxy, in which mandatory dogmas define group identity, and the essentially polythetic nature of Roman religious organization, in which incompatible beliefs could exist simultaneously in the community without conflict. In explaining how such beliefs could coexist in Rome, the study emphasizes three main (...)
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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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  • Natural categories and natural concepts.Frank C. Keil - 1981 - Behavioral and Brain Sciences 4 (2):293-294.
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  • Categorization and affordances.Rebecca K. Jones & Anne D. Pick - 1981 - Behavioral and Brain Sciences 4 (2):292-293.
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  • ‘Species-typicality’: Can individuals have typical parts?Timothy D. Johnston - 1981 - Behavioral and Brain Sciences 4 (2):291-292.
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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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  • The polythetic perspective.Donald D. Jensen - 1988 - Behavioral and Brain Sciences 11 (4):637-637.
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  • Metaphysics and common usage.David L. Hull - 1981 - Behavioral and Brain Sciences 4 (2):290-291.
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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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  • Behavior-genetic analysis versus ontogenetic imperialism.Jerry Hirsch - 1988 - Behavioral and Brain Sciences 11 (4):635-636.
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  • Universals, particulars, and paradigms.Helen Heise - 1981 - Behavioral and Brain Sciences 4 (2):289-290.
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  • The Statistical Frame of Mind in Systematic Biology from Quantitative Zoology to Biometry.Joel Hagen - 2003 - Journal of the History of Biology 36 (2):353-384.
    The twentieth century witnessed a dramatic increase in the use of statistics by biologists, including systematists. The modern synthesis and new systematics stimulated this development, particularly after World War II. The rise of "the statistical frame of mind " resulted in a rethinking of the relationship between biological and mathematical points of view, the roles of objectivity and subjectivity in systematic research, the implications of new computing technologies, and the place of systematics among the biological disciplines.
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  • The individuality thesis (3 ways).Matthew H. Haber - 2016 - Biology and Philosophy 31 (6):913-930.
    I spell out and update the individuality thesis, that species are individuals, and not classes, sets, or kinds. I offer three complementary presentations of this thesis. First, as a way of resolving an inconsistent triad about natural kinds; second, as a phylogenetic systematics theoretical perspective; and, finally, as a novel recursive account of an evolved character. These approaches do different sorts of work, serving different interests. Presenting them together produces a taxonomy of the debates over the thesis, and isolates ways (...)
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  • “Template theory” is heuristic in disentangling organism–environment interactions.Hans-Rudolf Güttinger - 1988 - Behavioral and Brain Sciences 11 (4):634-635.
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  • Nature/nurture and other dichotomies.Eugene S. Gollin - 1988 - Behavioral and Brain Sciences 11 (4):633-634.
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  • Taxa, life, and thinking.Michael T. Ghiselin - 1981 - Behavioral and Brain Sciences 4 (2):303-313.
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  • Phylogenetic Inference and the Misplaced Premise of Substitution Rates.Kirk Fitzhugh - 2021 - Acta Biotheoretica 69 (4):799-819.
    Three competing ‘methods’ have been endorsed for inferring phylogenetic hypotheses: parsimony, likelihood, and Bayesianism. The latter two have been claimed superior because they take into account rates of sequence substitution. Can rates of substitution be justified on its own accord in inferences of explanatory hypotheses? Answering this question requires addressing four issues: (1) the aim of scientific inquiry, (2) the nature of why-questions, (3) explanatory hypotheses as answers to why-questions, and (4) acknowledging that neither parsimony, likelihood, nor Bayesianism are inferential (...)
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  • Individuality and comparative biology.William L. Fink - 1981 - Behavioral and Brain Sciences 4 (2):288-289.
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  • A study of the science of taste: On the origins and influence of the core ideas.Robert P. Erickson - 2008 - Behavioral and Brain Sciences 31 (1):59-75.
    Our understanding of the sense of taste is largely based on research designed and interpreted in terms of the traditional four tastes: sweet, sour, salty, and bitter, and now a few more. This concept of basic tastes has no rational definition to test, and thus it has not been tested. As a demonstration, a preliminary attempt to test one common but arbitrary psychophysical definition of basic tastes is included in this article; that the basic tastes are unique in being able (...)
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  • A new cladistics of cladists.Malte C. Ebach, Juan J. Morrone & David M. Williams - 2008 - Biology and Philosophy 23 (1):153-156.
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  • Kinds of kinds: Individuality and biological species.Ronald de Sousa - 1989 - International Studies in the Philosophy of Science 3 (2):119 – 135.
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  • Phylogenetic classification.Claudio Gnoli - 2006 - Knowledge Organization 33 (3):138-152.
    One general principle in the construction of classification schemes is that of grouping phenomena to be classified according to their shared origin in evolution or history (phylogenesis). In general schemes, this idea has been applied by several classificationists in identifying a series of integrative levels, each originated from the previous ones, and using them as the main classes. In special schemes, common origin is a key principle in many domains: examples are given from the classification of climates, of organisms, and (...)
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  • Kinship Past, Kinship Present: Bio-Essentialism in the Study of Kinship.Robert A. Wilson - 2016 - American Anthropologist 118 (3).
    In this article, I reconsider bio-essentialism in the study of kinship, centering on David Schneider’s influential critique that concluded that kinship was “a non-subject” (1972:51). Schneider’s critique is often taken to have shown the limitations of and problems with past views of kinship based on biology, genealogy, and reproduction, a critique that subsequently led those reworking kinship as relatedness in the new kinship studies to view their enterprise as divorced from such bio-essentialist studies. Beginning with an alternative narrative connecting kinship (...)
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  • A Theory of Conceptual Advance: Explaining Conceptual Change in Evolutionary, Molecular, and Evolutionary Developmental Biology.Ingo Brigandt - 2006 - Dissertation, University of Pittsburgh
    The theory of concepts advanced in the dissertation aims at accounting for a) how a concept makes successful practice possible, and b) how a scientific concept can be subject to rational change in the course of history. Traditional accounts in the philosophy of science have usually studied concepts in terms only of their reference; their concern is to establish a stability of reference in order to address the incommensurability problem. My discussion, in contrast, suggests that each scientific concept consists of (...)
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  • A history of character concepts in evolutionary biology.Kurt M. Fristrup - 2001 - In G. P. Wagner (ed.), The Character Concept in Evolutionary Biology. Academic Press. pp. 15--37.
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  • Os dinossauros de Hennig: sobre a importância do monofiletismo para a sistemática biológica.Charles Morphy Dias dos Santos - 2008 - Scientiae Studia 6 (2):179-200.
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