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  1. Phylogenic and ontogenic environments.B. F. Skinner - 1984 - Behavioral and Brain Sciences 7 (4):701-711.
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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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  • Each behavior is a product of heredity and experience.Douglas Wahlsten - 1984 - Behavioral and Brain Sciences 7 (4):699-700.
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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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  • Skinner's practical metaphysic may be impractical.S. N. Salthe - 1984 - Behavioral and Brain Sciences 7 (4):696-697.
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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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  • 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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  • Molar concepts and mentalistic theories: A moral perspective.Stephen Kaplan - 1984 - Behavioral and Brain Sciences 7 (4):692-693.
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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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  • Behavior in the light of identified neurons.Graham Hoyle - 1984 - Behavioral and Brain Sciences 7 (4):690-691.
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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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  • Ethology ignored Skinner to its detriment.Jack P. Hailman - 1984 - Behavioral and Brain Sciences 7 (4):689-690.
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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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  • B. F. Skinner versus Dr. Pangloss.Michael T. Ghiselin - 1984 - Behavioral and Brain Sciences 7 (4):687-688.
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  • Skinner's blind eye.H. J. Eysenck - 1984 - Behavioral and Brain Sciences 7 (4):686-687.
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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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  • 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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  • 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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  • 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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  • Leaping up the phylogenetic scale in explaining anxiety: Perils and possibilities.Marvin Zuckerman - 1982 - Behavioral and Brain Sciences 5 (3):505-506.
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  • Role of the intrinsic modulatory systems in somesthesis.Tony L. Yaksh - 1980 - Behavioral and Brain Sciences 3 (2):315-315.
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  • The septo-hippocampal system and behavior: Difficulties in finding the exit.Michael L. Woodruff - 1982 - Behavioral and Brain Sciences 5 (3):504-504.
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  • A demonstration of persistent human avoidance in extinction.Richard W. Williams & Donald J. Levis - 1991 - Bulletin of the Psychonomic Society 29 (2):125-127.
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  • Enhancement of conditioned fear during extinction.Nicholas R. White & Paul T. P. Wong - 1982 - Bulletin of the Psychonomic Society 20 (5):272-274.
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  • A behavioral field analysis of adjunctive activities.Nicholas R. White & Paul T. P. Wong - 1982 - Bulletin of the Psychonomic Society 20 (5):266-268.
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  • Contextual determinants of pain reactions.Charles J. Vierck & Brian Y. Cooper - 1980 - Behavioral and Brain Sciences 3 (2):314-315.
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  • Bi-stability Of Emotions And Motivations: An evolutionary consequence of the open-ended capacity for learning.P. P. van der Molen - 1984 - Acta Biotheoretica 33 (4):227-251.
    Species, endowed with an open-ended capacity for learning, which is one of the highest evolutionary achievements,will profit most from this ability, if they are urged one way or other to invest any surplus of energy in expanding and refining their behavioural repertoire and in adapting it to prevailing circumstances, while incurring as little risk and stress as possible.It is therefore argued that an open-ended capacity for learning is maximally adding to survival if paired to two distinct tendencies: a tendency to (...)
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  • Pain is pain and fear is fear.Holger Ursin - 1982 - Behavioral and Brain Sciences 5 (2):318-320.
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  • Substrates of anxiety: But if the starting point is wrong?Holger Ursin - 1982 - Behavioral and Brain Sciences 5 (3):503-504.
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  • Functions and effects of Pavlovian stimuli.Jaylan Sheila Turkkan - 1993 - Behavioral and Brain Sciences 16 (2):394-398.
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  • Stimulus correlations in complex operant settings.François Tonneau - 1993 - Behavioral and Brain Sciences 16 (2):393-394.
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  • Inferring anxiety and antianxiety effects in animals.Philippe Soubrié - 1982 - Behavioral and Brain Sciences 5 (3):502-503.
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  • Does hippocampal theta tell us anything about the neuropsychology of anxiety?Terry E. Robinson & Barbara A. Therrien - 1982 - Behavioral and Brain Sciences 5 (3):500-502.
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  • The dynamics of action and the neuropsychology of anxiety.William Revelle - 1982 - Behavioral and Brain Sciences 5 (3):499-499.
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  • The relationship between memory and anxiety.J. N. P. Rawlins - 1982 - Behavioral and Brain Sciences 5 (3):498-499.
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  • The anatomy of anxiety?Karl H. Pribram & Diane McGuinness - 1982 - Behavioral and Brain Sciences 5 (3):496-498.
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  • The conditioning model of neurosis: promise and limitations.Roger K. Pitman - 1980 - Behavioral and Brain Sciences 3 (3):462-463.
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  • A multivalued logical net modelling conditioning.Vaclav Pinkava - 1980 - Behavioral and Brain Sciences 3 (3):461-462.
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  • Anxiety viewed from the upper brain stem: Though panic and fear yield trepidation, should both be called anxiety?Jaak Panksepp - 1982 - Behavioral and Brain Sciences 5 (3):495-496.
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  • Functions of the septo-hippocampal system.David S. Olton - 1982 - Behavioral and Brain Sciences 5 (3):494-495.
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  • On novelty, places, and the septo-hippocampal system.Lynn Nadel & Richard Morris - 1982 - Behavioral and Brain Sciences 5 (3):493-494.
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