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  1. Distinguishing between acts and patterns.Eliot Shimoff - 1995 - Behavioral and Brain Sciences 18 (1):142-142.
    The costliness of disrupting a pattern may not be a useful criterion for distinguishing between acts and patterns; there are instances in which omitted components of patterns are hard to detect (e.g., typographical errors), or in which distortions are easily introduced (e.g., slurred words in a trite phrase). Are there behavioral criteria for distinguishing between acts and patterns?
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  • The extended psychological present.Philip N. Hineline - 1995 - Behavioral and Brain Sciences 18 (1):128-129.
    Portraying psychological process as extended over time in multiply overlapping scales is a conceptual advance that can be understood as analogous to our understanding of spatial relationships. There may be a residual contradiction, however, when Rachlin invokes in ways that seem to imply earlier conceptions. The roles of superimposed or conditionally related stimuli also remain to be addressed.
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  • Foraging for a science of behavior.Michael Davison - 1985 - Behavioral and Brain Sciences 8 (2):335-336.
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  • The cost of an interrupted response pattern.Thomas R. Zentall - 1995 - Behavioral and Brain Sciences 18 (1):147-148.
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  • Resistance of “recovery” flavors to later association with illness.Donna M. Zahorik & Carol A. Bean - 1975 - Bulletin of the Psychonomic Society 6 (3):309-312.
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  • Avoidance is in the head, not the genes.Everett J. Wyers - 1982 - Behavioral and Brain Sciences 5 (4):685-685.
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  • The validation problem.Donald M. Wilkie - 1985 - Behavioral and Brain Sciences 8 (2):349-350.
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  • Classical conditioning and the placebo effect.Ian Wickram - 1989 - Behavioral and Brain Sciences 12 (1):160-161.
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  • Classical conditioning: A manifestation of Bayesian neural learning.James Christopher Westland & Manfred Kochen - 1989 - Behavioral and Brain Sciences 12 (1):160-160.
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  • Thyme to touch: Infants possess strategies that protect them from dangers posed by plants.Annie E. Wertz & Karen Wynn - 2014 - Cognition 130 (1):44-49.
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  • Missing variables in studies of animal learning.Wally Welker - 1981 - Behavioral and Brain Sciences 4 (1):161-161.
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  • Pattern proliferation in teleological behaviorism.Bruce N. Waller - 1995 - Behavioral and Brain Sciences 18 (1):145-146.
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  • Associative learning: Stimulus arrangement and response consistency.Dieter Vaitl - 1995 - Behavioral and Brain Sciences 18 (2):314-315.
    Studies on associative learning in normals and patients need appropriate dependent measures which are sensitive enough to reflect stimulus-specific responses and also consider the context in which the conditioning takes place. Patient's fear responses, once acquired, seem to be maintained by specific cognitive biases such as individual belief systems and a tendency to stay consistent with their previous judgments.
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  • Classical conditioning beyond the reflex: An uneasy rebirth.Jaylan Sheila Turkkan - 1989 - Behavioral and Brain Sciences 12 (1):161-179.
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  • Advances toward a biological theory of aversive learning: Flirtation or commitment?Dallas Treit & Marcia L. Spetch - 1982 - Behavioral and Brain Sciences 5 (4):684-685.
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  • Disgust: Sensory affect or primary emotional system?Judith A. Toronchuk & George Fr Ellis - 2007 - Cognition and Emotion 21 (8):1799-1818.
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  • Further choices for molar theory.François Tonneau - 1995 - Behavioral and Brain Sciences 18 (1):145-145.
    The target article extends molar behaviorism in two positive ways: beyond average aggregates and beyond restricted laws of Although a molar framework based on purely overt events shows promise for advancing behavior theory, Rachlin's specific form of teleological behaviorism is in need of clarification.
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  • What is the critical evidence favoring expectancy bias theory, and where is it?Andrew J. Tomarken - 1995 - Behavioral and Brain Sciences 18 (2):313-314.
    Davey has failed to clarify the critical evidence that could corroborate the expectancy bias hypothesis and refute preparedness theory. Such a clarification is necessary because each theory could potentially allow for multiple distal and proximal influences on selective associations. Expectancies are not the only proximal mediators. Our recent findings indicate that affective response matching may be an additional factor promoting such associations.
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  • The modelling of incentive motivation processes.Frederick M. Toates - 1980 - Behavioral and Brain Sciences 3 (3):466-468.
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  • A cognitive-incentive view.Frederick M. Toates - 1982 - Behavioral and Brain Sciences 5 (4):683-684.
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  • Why would we ever doubt that species are intelligent?Nicholas S. Thompson - 1990 - Behavioral and Brain Sciences 13 (1):94-94.
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  • Overcoming contextual variables, negative results, and Macphail's null hypothesis.Roger K. Thomas - 1987 - Behavioral and Brain Sciences 10 (4):680.
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  • The role of discounting in global social issues.Craig Summers - 1995 - Behavioral and Brain Sciences 18 (1):144-144.
    The willingness to trade off large but ill-defined future consequences for immediate work characterizes social problems such as environmental sustainability. This commentary argues that important applications of behavioral models of self-control are being overlooked in the experimental literature. Tying the experimental literature to longterm health, environmental, and other risks makes the experimental work more germane, and raises new research questions for experimental modeling.
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  • Effective search using Sewall Wright's shifting balance hypothesis.B. H. Sumida - 1990 - Behavioral and Brain Sciences 13 (1):93-93.
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  • Neo-Lamarckism, or, The rediscovery of culture.Gary W. Strong - 1990 - Behavioral and Brain Sciences 13 (1):92-93.
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  • Of cockroaches as kings.Robert J. Sternberg - 1990 - Behavioral and Brain Sciences 13 (1):91-91.
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  • Phobias and anxiety in the framework of the defense reflex.E. N. Sokolov - 1995 - Behavioral and Brain Sciences 18 (2):313-313.
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  • Genetic aspects to differences in foraging behavior.Marla B. Sokolowski - 1985 - Behavioral and Brain Sciences 8 (2):348-349.
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  • Levels of explanation.Mark Snyderman - 1985 - Behavioral and Brain Sciences 8 (2):348-348.
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  • The conditioned response: More than a knee-jerk in the ontogeny of behavior.William P. Smotherman & Scott R. Robinson - 1989 - Behavioral and Brain Sciences 12 (1):159-160.
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  • Alternatives to radical behaviorism.Terry L. Smith - 1995 - Behavioral and Brain Sciences 18 (1):143-144.
    Operant psychologists are looking for alternatives to radical behaviorism. Rachlin offers teleological behaviorism, but it may pose as many difficulties as radical behaviorism. There is, however, a less drastic way to defend Rachlin's thesis of It portrays operant principles as relating distal efficient causes to behavioral effects.
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  • Teleological behaviorism and internal control of behavior.Albert Silverstein - 1995 - Behavioral and Brain Sciences 18 (1):142-143.
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  • Core knowledge and its limits: The domain of food.Kristin Shutts, Kirsten F. Condry, Laurie R. Santos & Elizabeth S. Spelke - 2009 - Cognition 112 (1):120-140.
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  • The evolution of multiple memory systems.David F. Sherry & Daniel L. Schacter - 1987 - Psychological Review 94 (4):439-454.
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  • Questions about foraging.Sara J. Shettleworth - 1985 - Behavioral and Brain Sciences 8 (2):347-348.
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  • Natural selection and intelligence.David F. Sherry - 1987 - Behavioral and Brain Sciences 10 (4):678.
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  • Intelligence: More than a matter of associations.Sara J. Shettleworth - 1987 - Behavioral and Brain Sciences 10 (4):679.
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  • An ecological theory of learning: Good goal, poor strategy.Sara J. Shettleworth - 1981 - Behavioral and Brain Sciences 4 (1):160-161.
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  • The ecology of learning: The right answer to the wrong question.Barry Schwartz - 1981 - Behavioral and Brain Sciences 4 (1):159-160.
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  • Self-control: Acts of free will.James A. Schirillo - 1995 - Behavioral and Brain Sciences 18 (1):141-141.
    Rachlin overlooks that free will determines when and in what direction acts that appear impulsive will occur. Because behavioral patterns continuously evolve, animals are not guaranteed when they will, or how to, maximize larger-later reinforcements. An animal therefore uses self-control to emit free acts to vary behavioral patterns to optimize larger-later rewards.
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  • Responses conditioned to fear-relevant stimuli survive extinction of the expectancy of the UCS.Anne M. Schell & Michael E. Dawson - 1995 - Behavioral and Brain Sciences 18 (2):312-313.
    Davey suggests that increased resistance to extinction of CRs conditioned to fear-relevant stimuli may be due to more persistent expectancies of the UCS following these stimuli. However, this viewpoint is contradicted by existing empirical evidence that fear-relevant CRs survive an extinction trials series producing extinction of expectancies whereas CRs conditioned to non-fear-relevant CSs do not.
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  • Are species intelligent?: Not a yes or no question.Jonathan Schull - 1990 - Behavioral and Brain Sciences 13 (1):94-108.
    Plant and animal species are information-processing entities of such complexity, integration, and adaptive competence that it may be scientifically fruitful to consider them intelligent. The possibility arises from the analogy between learning and evolution, and from recent developments in evolutionary science, psychology and cognitive science. Species are now described as spatiotemporally localized individuals in an expanded hierarchy of biological entities. Intentional and cognitive abilities are now ascribed to animal, human, and artificial intelligence systems that process information adaptively, and that manifest (...)
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  • Are species intelligent?: Not a yes or no question.Jonathan Schull - 1990 - Behavioral and Brain Sciences 13 (1):63-75.
    Plant and animal species are information-processing entities of such complexity, integration, and adaptive competence that it may be scientifically fruitful to consider them intelligent. The possibility arises from the analogy between learning and evolution, and from recent developments in evolutionary science, psychology and cognitive science. Species are now described as spatiotemporally localized individuals in an expanded hierarchy of biological entities. Intentional and cognitive abilities are now ascribed to animal, human, and artificial intelligence systems that process information adaptively, and that manifest (...)
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  • Is simulated foraging similar to natural foraging?Masaya Sato & Takayuki Sakagami - 1985 - Behavioral and Brain Sciences 8 (2):346-347.
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  • Classical conditioning and language: The old hegemony.Vincent J. Samar & Gerald P. Berent - 1989 - Behavioral and Brain Sciences 12 (1):158-159.
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  • Misplaced predicates and misconstrued intelligence.Stanley N. Salthe - 1990 - Behavioral and Brain Sciences 13 (1):86-87.
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  • “Intelligence” as description and as explanation.P. A. Russell - 1990 - Behavioral and Brain Sciences 13 (1):86-86.
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  • Explaining diversity and searching for general processes: Isn't there a middle ground?Paul Rozin - 1981 - Behavioral and Brain Sciences 4 (1):157-158.
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  • Of rats and men.Neil Rowland - 1985 - Behavioral and Brain Sciences 8 (2):346-346.
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  • Metacomparative psychology.Herbert L. Roitblat - 1987 - Behavioral and Brain Sciences 10 (4):677.
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