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  1. Precursors to what? Theory is lacking for handedness in humans.Yves Guiard - 1987 - Behavioral and Brain Sciences 10 (2):276-277.
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  • Does a hand preference indicate a hemispheric specialization?Herbert Heuer - 1987 - Behavioral and Brain Sciences 10 (2):277-278.
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  • Evolution of handedness.Marjorie LeMay - 1987 - Behavioral and Brain Sciences 10 (2):281-281.
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  • Visually guided reaching in adult baboons.Jacques Vauclair & Joël Fagot - 1987 - Behavioral and Brain Sciences 10 (2):287-287.
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  • The concept of association cortex should be abandoned.E. J. Neafsey - 1988 - Behavioral and Brain Sciences 11 (1):97-97.
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  • Cetacean brains have a structure similar to the brains of primitive mammals; does this imply limits in function?John F. Eisenberg - 1988 - Behavioral and Brain Sciences 11 (1):92-92.
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  • Developmental axes and evolutionary trees.G. M. Innocenti - 1988 - Behavioral and Brain Sciences 11 (1):94-95.
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  • Intelligent neurons.G. Székely - 1987 - Behavioral and Brain Sciences 10 (3):388-389.
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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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  • Ethological invariants: Boxes, rubber bands, and biological processes.John C. Fentress - 1987 - Behavioral and Brain Sciences 10 (3):377-378.
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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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  • Ethology and physiology: A happy marriage.Gerard P. Baerends - 1987 - Behavioral and Brain Sciences 10 (3):369-370.
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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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  • Connectionist models are also algorithmic.David S. Touretzky - 1987 - Behavioral and Brain Sciences 10 (3):496-497.
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  • Archetypes: Toward a Jungian Anthropology of Consciousness.Charles D. Laughlin & Vincenza A. Tiberia - 2012 - Anthropology of Consciousness 23 (2):127-157.
    It is very curious that C.G. Jung has had so little influence upon the anthropology of consciousness. In this paper, the reasons for this oversight are given. The archetypal psychology of Jung is summarized and shown to be more complex and useful than extreme constructivist accounts would acknowledge. Jung's thinking about consciousness fits very well with a modern neuroscience view of the psyche and acts as a corrective to relativist notions of consciousness and its relation to the self.
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  • Syntax as an Emergent Characteristic of the Evolution of Semantic Complexity.P. Thomas Schoenemann - 1999 - Minds and Machines 9 (3):309-346.
    It is commonly argued that the rules of language, as distinct from its semantic features, are the characteristics which most clearly distinguish language from the communication systems of other species. A number of linguists (e.g., Chomsky 1972, 1980; Pinker 1994) have suggested that the universal features of grammar (UG) are unique human adaptations showing no evolutionary continuities with any other species. However, recent summaries of the substantive features of UG are quite remarkable in the very general nature of the features (...)
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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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  • The algorithm/implementation distinction.Austen Clark - 1987 - Behavioral and Brain Sciences 10 (3):480-480.
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  • Some agenda items for a neurobiology of cognition: An introduction.Peter D. Eimas & Albert M. Galaburda - 1989 - Cognition 33 (1-2):1-23.
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  • Primate handedness should be considered – but not “reconsidered” at this point.Walter F. McKeever - 1987 - Behavioral and Brain Sciences 10 (2):281-282.
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  • Ontogenetic considerations in the phylogenetic history and adaptive significance of the bias in human handedness.George F. Michel & Debra A. Harkins - 1987 - Behavioral and Brain Sciences 10 (2):283-284.
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  • But what about nonprimate asymmetries and nonmanual primate asymmetries?John L. Bradshaw - 1987 - Behavioral and Brain Sciences 10 (2):264-265.
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  • Primate handedness reconsidered.Peter F. MacNeilage, Michael G. Studdert-Kennedy & Bjorn Lindblom - 1987 - Behavioral and Brain Sciences 10 (2):247-263.
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  • The “initial” brain concept: Its uses and misuses.Ilya I. Glezer, Myron S. Jacobs & Peter J. Morgane - 1988 - Behavioral and Brain Sciences 11 (1):106-116.
    We review the evidence for the concept of the “initial” or prototype brain. We outline four possible modes of brain evolution suggested by our new findings on the evolutionary status of the dolphin brain. The four modes involve various forms of deviation from and conformity to the hypothesized initial brain type. These include examples of conservative evolution, progressive evolution, and combinations of the two in which features of one or the other become dominant. The four types of neocortical organization in (...)
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  • Elephants have a large neocortex too.Jeheskel Shoshani - 1988 - Behavioral and Brain Sciences 11 (1):100-100.
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  • Determining species differences in numbers of cortical areas and modules: The architectonic method needs supplementation.Jon H. Kaas - 1988 - Behavioral and Brain Sciences 11 (1):96-97.
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  • Putting all cetacean brains in one category is a big order.Sue T. Parker - 1988 - Behavioral and Brain Sciences 11 (1):97-98.
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  • What about Sirenia?Bernhard Rensch - 1988 - Behavioral and Brain Sciences 11 (1):99-99.
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  • Fish, sea snakes, dolphins, teeth and brains – some evolutionary paradoxes.Kathleen R. Gibson - 1988 - Behavioral and Brain Sciences 11 (1):93-94.
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  • Whose brain is initial-like?John Irwin Johnson - 1988 - Behavioral and Brain Sciences 11 (1):96-96.
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  • Conservative aspects of the dolphin cortex match its behavioral level.Lester R. Aronson & Ethel Tobach - 1988 - Behavioral and Brain Sciences 11 (1):89-90.
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  • Parcellation and plasticity: Implications for ontogeny.Mark Johnson - 1988 - Behavioral and Brain Sciences 11 (3):547.
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  • Networks with evolutionary potential.Günter Ehret - 1987 - Behavioral and Brain Sciences 10 (3):376-377.
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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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  • How is a toad not like a bug?Jeffrey M. Camhi - 1987 - Behavioral and Brain Sciences 10 (3):371-372.
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  • Connectionism and implementation.Paul Smolensky - 1987 - Behavioral and Brain Sciences 10 (3):492-493.
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  • Methodologies for studying human knowledge.John R. Anderson - 1987 - Behavioral and Brain Sciences 10 (3):467-477.
    The appropriate methodology for psychological research depends on whether one is studying mental algorithms or their implementation. Mental algorithms are abstract specifications of the steps taken by procedures that run in the mind. Implementational issues concern the speed and reliability of these procedures. The algorithmic level can be explored only by studying across-task variation. This contrasts with psychology's dominant methodology of looking for within-task generalities, which is appropriate only for studying implementational issues.The implementation-algorithm distinction is related to a number of (...)
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  • Many levels: More than one is algorithmic.Michael A. Arbib - 1987 - Behavioral and Brain Sciences 10 (3):478-479.
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  • Natural Language and the Propositional Attitude Complex.Karen Shanton - 2006 - SWIF Philosophy of Mind Review 5 (3).
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  • Which hand lost its cunning?Harry J. Jerison - 1987 - Behavioral and Brain Sciences 10 (2):278-279.
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  • On the other hand ….Ralph A. W. Lehman - 1987 - Behavioral and Brain Sciences 10 (2):280-281.
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  • Handedness as chance or as species characteristic.Marian Annett - 1987 - Behavioral and Brain Sciences 10 (2):263-264.
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  • Handedness is a matter of degree.M. P. Bryden & Runa E. Steenhuis - 1987 - Behavioral and Brain Sciences 10 (2):266-267.
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  • Why the left hand?Michael Tomasello - 1987 - Behavioral and Brain Sciences 10 (2):286-287.
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  • Or in the hand, or in the heart? Alternative routes to lateralization.Stephen Walker - 1987 - Behavioral and Brain Sciences 10 (2):288-288.
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  • Elegant hypotheses are intellectually rewarding; even more so if more hard data were available.János Szentágothai - 1988 - Behavioral and Brain Sciences 11 (1):102-102.
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  • Implications of the “initial brain” concept for brain evolution in Cetacea.Ilya I. Glezer, Myron S. Jacobs & Peter J. Morgane - 1988 - Behavioral and Brain Sciences 11 (1):75-89.
    We review the evidence for the concept of the “initial” or prototype brain. We outline four possible modes of brain evolution suggested by our new findings on the evolutionary status of the dolphin brain. The four modes involve various forms of deviation from and conformity to the hypothesized initial brain type. These include examples of conservative evolution, progressive evolution, and combinations of the two in which features of one or the other become dominant. The four types of neocortical organization in (...)
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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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  • More than meets the eye.Russell D. Fernald - 1987 - Behavioral and Brain Sciences 10 (3):378-379.
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  • Connectionism and motivation are compatible.Daniel S. Levine - 1987 - Behavioral and Brain Sciences 10 (3):487-487.
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