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  1. Four-Dimensional Consciousness.Richard Allen Sieb - 2017 - Activitas Nervosa Superior 59 (2):(43-60).
    Conscious experience is the direct observation of conscious events. Human conscious experience is four-dimensional. Conscious events are linked (associated) by spacetime intervals to produce a coherent conscious experience. This explains why conscious experience appears to us the way it does. Conscious experience is an orientation in space and time, an understanding of the position of the observer in space and time. Causality, past-future relations, learning, memory, cognitive processing, and goal-directed actions all evolve from four-dimensional conscious experience. A neural correlate for (...)
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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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  • 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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  • 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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  • 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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  • 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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  • The role of the extrapersonal brain systems in religious activity.Fred H. Previc - 2006 - Consciousness and Cognition 15 (3):500-539.
    The neuropsychology of religious activity in normal and selected clinical populations is reviewed. Religious activity includes beliefs, experiences, and practice. Neuropsychological and functional imaging findings, many of which have derived from studies of experienced meditators, point to a ventral cortical axis for religious behavior, involving primarily the ventromedial temporal and frontal regions. Neuropharmacological studies generally point to dopaminergic activation as the leading neurochemical feature associated with religious activity. The ventral dopaminergic pathways involved in religious behavior most closely align with the (...)
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  • Qualitative navigation for mobile robots.Tod S. Levitt & Daryl T. Lawton - 1990 - Artificial Intelligence 44 (3):305-360.
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  • Sampling and information processing.Edward Gruberg - 1987 - Behavioral and Brain Sciences 10 (3):381-382.
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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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  • 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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  • Presumptions based on keyhole peeping.G. A. Horridge - 1987 - Behavioral and Brain Sciences 10 (3):382-383.
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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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  • Implicit versus explicit computation.Kent A. Stevens - 1987 - Behavioral and Brain Sciences 10 (3):387-388.
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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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  • Intelligent neurons.G. Székely - 1987 - Behavioral and Brain Sciences 10 (3):388-389.
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  • Networks with evolutionary potential.Günter Ehret - 1987 - Behavioral and Brain Sciences 10 (3):376-377.
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  • Exploration and memory.Catherine Thinus-Blanc - 1988 - Behavioral and Brain Sciences 11 (3):552.
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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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  • 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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  • Ewert's model: Some discoveries and some difficulties.David Ingle - 1987 - Behavioral and Brain Sciences 10 (3):383-385.
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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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  • Memory – we had not forgotten.Nigel Foreman & Robin Stevens - 1988 - Behavioral and Brain Sciences 11 (3):554.
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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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  • 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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  • 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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  • 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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