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  1. Affective Neuroscience: Past, Present, and Future.Tim Dalgleish, Barnaby D. Dunn & Dean Mobbs - 2009 - Emotion Review 1 (4):355-368.
    The discipline of affective neuroscience is concerned with the underlying neural substrates of emotion and mood. This review presents an historical overview of the pioneering work in affective neuroscience of James and Lange, Cannon and Bard, and Hess, Papez, and MacLean before summarizing the current state of research on the brain regions identified by these seminal researchers. We also discuss the more recent strides made in the field of affective neuroscience. A final section considers different hypothetical organizations of affective neuroanatomy (...)
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  • The physiological psychology of hunger: A physiological perspective.Mark I. Friedman & Edward M. Stricker - 1976 - Psychological Review 83 (6):409-431.
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  • Networks with evolutionary potential.Günter Ehret - 1987 - Behavioral and Brain Sciences 10 (3):376-377.
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  • Deconstructing the “Two Factors”: The Historical Origins of the Schachter–Singer Theory of Emotions.Otniel E. Dror - 2017 - Emotion Review 9 (1):7-16.
    In this contribution, I interrogate the historical-intellectual narrative that dominates the history of the Schachter–Singer two-factor theory of emotion. In the first part, I propose that a social influence model became generalized to a cognitive view. I argue that Schachter and Singer presented a cognitive theory of emotions in enacting inside the laboratory Schachter’s preceding “social influence” model of emotions and that Schachter’s adoption of a cognitive model of emotion was driven by and was necessary for his previous research on (...)
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  • Neuroethology and color vision in amphibians.S. L. Kondrashev - 1987 - Behavioral and Brain Sciences 10 (3):385-385.
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  • Neuroethology of releasing mechanisms: Prey-catching in toads.Jörg-Peter Ewert - 1987 - Behavioral and Brain Sciences 10 (3):337-368.
    Abstract“Sign stimuli” elicit specific patterns of behavior when an organism's motivation is appropriate. In the toad, visually released prey-catching involves orienting toward the prey, approaching, fixating, and snapping. For these action patterns to be selected and released, the prey must be recognized and localized in space. Toads discriminate prey from nonprey by certain spatiotemporal stimulus features. The stimulus-response relations are mediated by innate releasing mechanisms (RMs) with recognition properties partly modifiable by experience. Striato-pretecto-tectal connectivity determines the RM's recognition and localization (...)
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  • Presumptions based on keyhole peeping.G. A. Horridge - 1987 - Behavioral and Brain Sciences 10 (3):382-383.
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  • Evolutionary conceptions of adaptation and brain design.Jay Schulkin - 1989 - World Futures 27 (1):1-15.
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  • The nervous system/behavior interface: Levels of organization and levels of approach.Paul Grobstein - 1987 - Behavioral and Brain Sciences 10 (3):380-381.
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  • Eliminate the middletoad!Daniel Dennett - 1987 - Behavioral and Brain Sciences 10 (3):372-374.
    Philosophical controversy about the mind has flourished in the thin air of our ignorance about the brain. The humble toad, it now seems, may provide our first instance of a creature whose whole brain is within the reach of our scientific understanding. What will happen to the traditional philosophical issues as our theoretical and factual ignorance recedes? Discussion of the issues explored in the target article is, as Ewert says, "often too theoretical, sometimes philosophical and even [as if that weren't (...)
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  • Sensorimotor maps in the tectum.A. Roucoux & M. Crommelinck - 1987 - Behavioral and Brain Sciences 10 (3):386-387.
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  • Toward a reformulation of the command concept.Randolf DiDomenico & Robert C. Eaton - 1987 - Behavioral and Brain Sciences 10 (3):374-375.
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  • Intelligent neurons.G. Székely - 1987 - Behavioral and Brain Sciences 10 (3):388-389.
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  • Implicit versus explicit computation.Kent A. Stevens - 1987 - Behavioral and Brain Sciences 10 (3):387-388.
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  • Worm detector replaced by network model – but still a bit worm-infested.Gerhard Roth & Kiisa Nishikawa - 1987 - Behavioral and Brain Sciences 10 (3):385-386.
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  • Ewert's model: Some discoveries and some difficulties.David Ingle - 1987 - Behavioral and Brain Sciences 10 (3):383-385.
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  • Sampling and information processing.Edward Gruberg - 1987 - Behavioral and Brain Sciences 10 (3):381-382.
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  • The compleat visual system: From input to output.M. A. Goodale - 1987 - Behavioral and Brain Sciences 10 (3):379-380.
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  • More than meets the eye.Russell D. Fernald - 1987 - Behavioral and Brain Sciences 10 (3):378-379.
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  • Ethological invariants: Boxes, rubber bands, and biological processes.John C. Fentress - 1987 - Behavioral and Brain Sciences 10 (3):377-378.
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  • Toad's prey-catching: A complex system with heuristic value.Jörg-Peter Ewert - 1987 - Behavioral and Brain Sciences 10 (3):389-405.
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  • Prey-catching in toads: An exceptional neuroethological model.Seven O. E. Ebbesson - 1987 - Behavioral and Brain Sciences 10 (3):375-376.
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  • Has the greedy toad lost its soul; and if so, what was it?Robert W. Doty - 1987 - Behavioral and Brain Sciences 10 (3):375-375.
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  • Sensorimotor functions: What is a command, that a code may yield it?Christopher M. Comer - 1987 - Behavioral and Brain Sciences 10 (3):372-372.
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  • How is a toad not like a bug?Jeffrey M. Camhi - 1987 - Behavioral and Brain Sciences 10 (3):371-372.
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  • After the sensory analysers: Problems with concepts and terminology.D. M. Broom - 1987 - Behavioral and Brain Sciences 10 (3):370-371.
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  • Ethology and physiology: A happy marriage.Gerard P. Baerends - 1987 - Behavioral and Brain Sciences 10 (3):369-370.
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  • Advantages of experimentation in neuroscience.Michael A. Arbib - 1987 - Behavioral and Brain Sciences 10 (3):368-369.
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