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  1. Nonconscious motor images.Giacomo Rizzolatti - 1994 - Behavioral and Brain Sciences 17 (2):220-220.
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  • To dream is not to (intend to) do.Jean Requin - 1994 - Behavioral and Brain Sciences 17 (2):218-219.
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  • Motor images are action plans.Wolfgang Prinz - 1994 - Behavioral and Brain Sciences 17 (2):218-218.
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  • Précis of Images of Mind.Michael I. Posner & Marcus E. Raichle - 1995 - Behavioral and Brain Sciences 18 (2):327-339.
    This volume explores how functional brain imaging techniques like positron emission tomography have influenced cognitive studies. The first chapter outlines efforts to relate human thought and cognition in terms of great books from the late 1800s through the present. Chapter 2 describes mental operations as they are measured in cognitive science studies. It develops a framework for relating mental operations to activity in nerve cells. In Chapter 3, the PET method is reviewed and studies are presented that use PET to (...)
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  • Interaction of method and theory in cognitive neuroscience.Michael I. Posner & Marcus E. Raichle - 1995 - Behavioral and Brain Sciences 18 (2):372-383.
    We divided the many diverse comments on our book into categories. These are: theory, scope and goals of our project, methods, comments on specific anatomical areas, the concept of attention, consciousness and cognitive control, and finally other issues. Although many of the points of the critics are certainly well taken, we believe studies that have emerged since our book provide strong evidence that the general approach taken in our book is now yielding important new data on the relation of cognitive (...)
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  • Neuroimaging studies of language should connect with (psycho)linguistic theories.David Poeppel & Susan Johnson - 1995 - Behavioral and Brain Sciences 18 (2):369-370.
    PET studies in domains like vision and attention have been successful because the experiments are the product of highly articulated theories. In contrast, the results of PET studies investigating language processing are difficult to interpret. We suggest that this difficulty is due to the more tentative connection of these experiments with the insights of psycholinguistics and linguistic theory.
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  • A Connectionist Approach to Word Reading and Acquired Dyslexia: Extension to Sequential Processing.David C. Plaut - 1999 - Cognitive Science 23 (4):543-568.
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  • Neural images and neural coding.Antonio L. Perrone & Gianfranco Basti - 1995 - Behavioral and Brain Sciences 18 (2):368-369.
    In Posner & Raichle's (1994) book, two essential and strictly related limitations of cognitive neurophysiology are not sufficiently enhanced: (1) The problem of “coding,” namely the capability of a natural brain to redefine its own “basic symbols” as a function of a changing environment; (2) the inadequacy of a Hebbian rule to reckon with complex computational problems such as those solved by real brains.
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  • Representations of movement and representations in movement.Giuseppe Pellizzer & Apostolos P. Georgopoulos - 1994 - Behavioral and Brain Sciences 17 (2):216-217.
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  • Know thyself: Metacognitive networks and measures of consciousness.Antoine Pasquali, Bert Timmermans & Axel Cleeremans - 2010 - Cognition 117 (2):182-190.
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  • Neuroimaging: Beginning to Appreciate Its Complexities.Erik Parens & Josephine Johnston - 2014 - Hastings Center Report 44 (s2):2-7.
    For over a century, scientists have sought to see through the protective shield of the human skull and into the living brain. Today, an array of technologies allows researchers and clinicians to create astonishingly detailed images of our brain's structure as well as colorful depictions of the electrical and physiological changes that occur within it when we see, hear, think and feel. These technologies—and the images they generate—are an increasingly important tool in medicine and science.Given the role that neuroimaging technologies (...)
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  • If a picture is worth a thousand words, how many pictures is a word worth?Ken A. Paller - 1995 - Behavioral and Brain Sciences 18 (2):367-368.
    Pictures of normal brain activity during human thought can be worth a great deal. Electrophysiology and functional neuroimaging together allow both temporal and spatial dimensions of neurocognitive functions to be explored. Although these techniqueshave their limitations, the Cognitive Neuroscience approach is well-suited to pursuing questions about how words are perceived, understood, and remembered.
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  • Jeannerod's representing brain: Image or illusion?Jean Pailhous & Mireille Bonnard - 1994 - Behavioral and Brain Sciences 17 (2):215-216.
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  • Optimizing subjective measures of consciousness.Morten Overgaard, Bert Timmermans, Kristian Sandberg & Axel Cleeremans - 2010 - Consciousness and Cognition 19 (2):682-684.
    Dienes and Seth (2010) conclude that confidence ratings and post-decision wagering are two comparable and recommendable measures of conscious experience. In a recently submitted paper, we have however found that both methods are problematic and seem less suited to measure consciousness than a direct introspective measure. Here, we discuss the methodology and conclusions put forward by Dienes and Seth, and why we think the two experiments end up with so different recommendations.
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  • When is it sensible to use PET to study brain function?Shane M. O'Mara - 1995 - Behavioral and Brain Sciences 18 (2):366-367.
    Posner & Raichle's book is a superbly presented and wellwritten overview of a fast-developing and important field in contemporary neuroscience. It suffers from being an overview, however, because it does not go into sufficient detail or depth in many of the issues that it raises. It also neglects many other important areas of current research, for example, technical advances in other areas, learning and memory, and lesion analysis of brain function.
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  • Motor simulation.Adam Morton - 1994 - Behavioral and Brain Sciences 17 (2):215-215.
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  • Unconscious familiarity and local context effects on low-level face processing: A reconstruction hypothesis.Timothy Montoute & Guy Tiberghien - 2001 - Consciousness and Cognition 10 (4):503-523.
    A common view in face recognition research holds that there is a stored representation specific to each known face. It is also posited that semantic or memory-based information cannot influence low-level face processing. The two experiments reported in this article investigate the nature of this representation and the flow of face information processing. Participants had to search for a particular primed face among other faces. In Experiment 1, the search was done in a context where distractors had either a different (...)
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  • Are motor images based on kinestheticvisual matching?Robert W. Mitchell - 1994 - Behavioral and Brain Sciences 17 (2):214-215.
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  • Visually guided action and the “need to know”.A. David Milner, David P. Carey & Monika Harvey - 1994 - Behavioral and Brain Sciences 17 (2):213-214.
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  • The hominid tool-language connection: Some missing evolutionary links?A. Maryanski - 1995 - Behavioral and Brain Sciences 18 (1):199-200.
    This commentary criticizes Wilkins & Wakefield's thesis that the neurological precursors of language provide a cognitive Rubicon to linguistically divide human from nonhuman primates. A causal model of their theory is presented, followed by a discussion of the relationship between brain expansion and tool use, Broca's area and the parietaloccipital-temporal junction (POT).
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  • Dissociations in Neuropsychology and Cognitive Neuroscience.Edouard Machery - 2012 - Philosophy of Science 79 (4):490-518.
    In this article, I compare the epistemic standing of the function-to-structure inferences found in cognitive neuroscience and of the inferences based on dissociations in neuropsychology. I argue that the former have a poorer epistemic standing than the latter.
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  • Semiogenesis as a continuous, not a discrete, phenomenon.Jo Liska - 1995 - Behavioral and Brain Sciences 18 (1):198-199.
    This commentary confronts one of the central tenets advanced in Wilkins & Wakefield's target article: By adopting a very narrow perspective on language, the authors have effectively limited discussion of earlier linguistic capabilities thought to be at least facilitative of, if not prerequisite to language defined as a An alternative conceptualization for describing semiogenesis is offered.
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  • Naturalizing the acting self: Subjective vs. Anonymous agency.Dorothée Legrand - 2007 - Philosophical Psychology 20 (4):457 – 478.
    This paper considers critically the enterprise of naturalizing the subjective experience of acting intentionally. I specifically expose the limits of the model that conceives of agency as composed of two stages. The first stage consists in experiencing an anonymous intention without being conscious of it as anybody's in particular. The second stage disambiguates this anonymous experience thanks to a mechanism of identification and attribution answering the question: "who is intending to act?" On the basis of phenomenological, clinical, methodological and empirical (...)
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  • Is the human brain only responsive?Rumyana Kristeva-Feige & Bernd Feige - 1995 - Behavioral and Brain Sciences 18 (2):365-366.
    Posner & Raichle's (1994) book is a fascinating and readable account of the studies the authors have conducted on the localization of cognitive functions in the brain mainly using PET and EEC evoked potential methods. Our criticism concerns the underrepresentation of some imaging techniques (magnetoencephalography) and some forms of brain activity (spontaneous activity). Furthermore, the book leaves the reader with the impression that the brain only responds to external events.
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  • On the relation between motor imagery and visual imagery.Roberta L. Klatzky - 1994 - Behavioral and Brain Sciences 17 (2):212-213.
    Jeannerod's target article describes support, through empirical and neurological findings, for the intriguing idea of motor imagery, a form of representation hypothesized to have levels of functional equivalence with motor preparation, while being consciously accessible. Jeannerod suggests that the subjectively accessible content of motor imagery allows it to be distinguished from motor preparation, which is unconscious. Motor imagery is distinguished from visual imagery in terms of content. Motor images are kinesthetic in nature; they are parametrized by variables such as force (...)
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  • Looking for images of memory.Narinder Kapur - 1995 - Behavioral and Brain Sciences 18 (2):364-365.
    This is an excellent book but it lacks a detailed presentation and formulation of images of memory. Positron emission tomography (PET) findings sometimes raise more enigmatic questions than they answer, with differences between studies and differences with established lesion evidence. Perhaps the book could have been more critical in its analysis of these enigmas, covering more of the basic issues and assumptions underlying PET research.
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  • Synergy versus schema.P. C. Kainen - 1994 - Behavioral and Brain Sciences 17 (2):212-212.
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  • Redefining cognitive psychology.John Jonides & Patricia Reuter-Lorenz - 1995 - Behavioral and Brain Sciences 18 (2):363-364.
    Posner & Raichle illustrate how neuroimaging blends profitably with neuropsychology and electrophysiology to advance cognitive theory. Recognizing that there are limitations to each of these techniques, we nonetheless argue that their confluence has fundamentally changed the way cognitive psychologists think about problems of the mind.
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  • Issues in neo- and paleoneurology of language.Harry J. Jerison - 1995 - Behavioral and Brain Sciences 18 (1):195-196.
    Wilkins and Wakefield's hypothesis that language is fundamentally a cognitive rather than cominunicational adaptation is reasonable, but there are flaws in their anatomical and fossil evidence. Their analysis of reorganization also needs clarification. Finally, the origin of language ability must have occurred with australopithecine rather than habiline adaptations on entry into the novel hominid adaptive zone.
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  • The representing brain: Neural correlates of motor intention and imagery.Marc Jeannerod - 1994 - Behavioral and Brain Sciences 17 (2):187-202.
    This paper concerns how motor actions are neurally represented and coded. Action planning and motor preparation can be studied using a specific type of representational activity, motor imagery. A close functional equivalence between motor imagery and motor preparation is suggested by the positive effects of imagining movements on motor learning, the similarity between the neural structures involved, and the similar physiological correlates observed in both imaging and preparing. The content of motor representations can be inferred from motor images at a (...)
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  • Motor representations and reality.M. Jeannerod - 1994 - Behavioral and Brain Sciences 17 (2):229-245.
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  • What is coded in parietal representations?Ray Jackendoff & Barbara Landau - 1994 - Behavioral and Brain Sciences 17 (2):211-212.
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  • Mind mappers and cognitive modelers: Toward cross-fertilization.Arthur M. Jacobs & Thomas H. Carr - 1995 - Behavioral and Brain Sciences 18 (2):362-363.
    It is argued that current neuroimaging studies can provide useful constraints for the construction of models of cognition, and that these studies should be guided by cognitive models. A numberof challenges for a successful cross-fertilization between “mind mappers” and cognitive modelers are discussed in the light of current research on word recognition.
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  • Language as a multimodal sensory enhancement system.Bob Jacobs & John M. Horner - 1995 - Behavioral and Brain Sciences 18 (1):194-195.
    Several claims made by Wilkins & Wakefield require qualification. First, the proposed delineation of the parietal-occipital-temporal junction (POT) is overly restrictive. Second, focusing exclusively on the evolutionary importance of manual manipulation oversimplifies interacting evolutionary preconditions for language. Finally, Wilkins and Wakefield's perspective adheres to a homocentric, formal, linguistic definition of language instead of viewing language as a multimodal sensory enhancement system unique to each species.
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  • Multiple scales of brain-mind interactions.Lester Ingber - 1995 - Behavioral and Brain Sciences 18 (2):360-362.
    Posner & Raichle'sImages of mindis an excellent educational book and very well written. Some flaws as a scientific publication are: (a) the accuracy of the linear subtraction method used in PET is subject to scrutiny by further research at finer spatial-temporal resolutions; (b) lack of accuracy of the experimental paradigm used for EEG complementary studies.
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  • Motor memory – a memory of the future.David H. Ingvar - 1994 - Behavioral and Brain Sciences 17 (2):210-211.
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  • Regions, networks: Interpreting functional neuroimaging data.Barry Horwitz - 1995 - Behavioral and Brain Sciences 18 (2):360-360.
    The subtraction and covariance paradigms are two analytic techniques used with functional neuroimaging data. The first assumes that a brain region participating in a task should show altered neural activity (relative to a control task). The second assumes that tasks are mediated by networks of interacting regions.Images of mindattempts to link results from the subtraction paradigm with a network interpretation that could have been more explicitly done using the covariance paradigm.
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  • Evidence for POT expansion in early Homo: A pretty theory with ugly (or no) paleoneurological facts.Ralph L. Holloway - 1995 - Behavioral and Brain Sciences 18 (1):191-193.
    If POT (parieto-occipital-temporal junction) reorganization came earlier in australopithecines than in Homo, it is likely that the selective pressures were different, and not necessarily directed toward language. The brain endocast evidence for the POT in A. afarensis is actually better than it is for early Homo.
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  • Human language: Are nonhuman precursors lacking?Marc D. Hauser & Nathan D. Wolfea - 1995 - Behavioral and Brain Sciences 18 (1):190-191.
    Contra Wilkins & Wakefield, we argue that an evolutionarily inspired approach to language must consider different facets of language (i.e., more than syntax and semantics), and must explore the possibility of nonhuman precursors. Several examples are discussed, illustrating the power of the comparative approach in illuminating our understanding of language evolution.
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  • Tracking brain functions in space and time.Riitta Hari - 1995 - Behavioral and Brain Sciences 18 (2):359-360.
    The authors ofImages of mindhave been highly successful in unravelling the neural basis of complex brain functions. Their emphasis on top-down processingin experimental neuroscience is especially important and, it is hoped, influential. Tracking brain activation accurately botli in space and in time would benefit from studiesofindividual subjects without relying on grand average data.
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  • PET may image the gates of awareness, not its center.Eric Halgren - 1995 - Behavioral and Brain Sciences 18 (2):358-359.
    PET detects changes in metabolism between task periods and is thus insensitive to areas that are activated during all or most of cognition. Depth-recorded, evokedpotentials indicate that many multimodal and limbic cortical areas may be activated during most cognitive tasks. Thus, PET may be insensitive to some core processes of awareness that are difficult to eliminate from the control periods.
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  • Involvement of primary motor cortex in motor imagery and mental practice.Mark Hallett, Jordan Fieldman, Leonardo G. Cohen, Norihiro Sadato & Alvaro Pascual-Leone - 1994 - Behavioral and Brain Sciences 17 (2):210-210.
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  • Motor models as steps to higher cognition.Rick Grush - 1994 - Behavioral and Brain Sciences 17 (2):209-210.
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  • Fables of the prefrontal cortex.Jordan Grafman, Arnaud Partiot & Caroline Hollnagel - 1995 - Behavioral and Brain Sciences 18 (2):349-358.
    On the basis of neuroiinaging studies, Posner & Raichle summarily report that the prefrontal cortex is involved in executive functioning and attention. In contrast to that superficial view, we briefly describe a testable model of the kinds of representations that are stored in prefrontal cortex, which, when activated, are expressed via plans, actions, thematic knowledge, and schemas.
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  • The neurodynamics of heavy PETing, at/intention, learning, functional recovery, and rehabilitation.Gary Goldberg & Nathaniel H. Mayer - 1995 - Behavioral and Brain Sciences 18 (2):348-349.
    Research reported by Posner & Raichle may be usefully applied to the rehabilitation of persons with brain damage. Their findings are related to the “dual premotorsystems hypothesis” that reciprocally interactive medial and lateral brain systems are involved in attention and learning. Recent studies show that “brain healing” occurs through dynamic reorganization involving attentional networks postulated by Posner & Raichle.
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  • Images in search of a theory.Ben Goertzel - 1995 - Behavioral and Brain Sciences 18 (2):347-348.
    Images of mindis an exciting book, well-written and wellorganized, but many of the connections the authors draw between PET scan results and more general psychological issues are somewhat strained.
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  • Separate visual representations in the planning and control of action.Scott Glover - 2004 - Behavioral and Brain Sciences 27 (1):3-24.
    Evidence for a dichotomy between the planning of an action and its on-line control in humans is reviewed. This evidence suggests that planning and control each serve a specialized purpose utilizing distinct visual representations. Evidence from behavioral studies suggests that planning is influenced by a large array of visual and cognitive information, whereas control is influenced solely by the spatial characteristics of the target, including such things as its size, shape, orientation, and so forth. Evidence from brain imaging and neuropsychology (...)
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  • Solving the language origins puzzle: Collecting and assembling all pertinent pieces.Kathleen R. Gibson - 1995 - Behavioral and Brain Sciences 18 (1):189-190.
    Wilkins & Wakefield fall short of solving the language origin puzzle because they underestimate the cognitive and linguistic capacities of great apes. A focus on ape capacities leads to the recognition of varied levels of cognition and language and to a gradualistic model of language emergence in which early hominid language skills exceed those of the apes but fall far short of those of modern humans or later fossil hominid groups.
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  • Peripheral and central correlates of attempted voluntary movements.S. C. Gandevia - 1994 - Behavioral and Brain Sciences 17 (2):208-209.
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  • Call it what it is: Motor memory.Joaquin M. Fuster - 1994 - Behavioral and Brain Sciences 17 (2):208-208.
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