Search results for '*Short Term Memory' (try it on Scholar)

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  1. Nelson Cowan (2001). The Magical Number 4 in Short-Term Memory: A Reconsideration of Mental Storage Capacity. Behavioral and Brain Sciences 24 (1):87-114.score: 120.0
    Miller (1956) summarized evidence that people can remember about seven chunks in short-term memory (STM) tasks. However, that number was meant more as a rough estimate and a rhetorical device than as a real capacity limit. Others have since suggested that there is a more precise capacity limit, but that it is only three to five chunks. The present target article brings together a wide variety of data on capacity limits suggesting that the smaller capacity limit is real. (...)
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  2. Paul Muter (2001). The Nature of Forgetting From Short-Term Memory. Behavioral and Brain Sciences 24 (1):134-134.score: 120.0
    Memory and forgetting are inextricably intertwined. Any account of short-term memory (STM) should address the following question: If three, four, or five chunks are being held in STM, what happens after attention is diverted?
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  3. Bart Rypma & John D. E. Gabrieli (2001). Functional Neuroimaging of Short-Term Memory: The Neural Mechanisms of Mental Storage. Behavioral and Brain Sciences 24 (1):143-144.score: 120.0
    Cowan argues that the true short-term memory (STM) capacity limit is about 4 items. Functional neuroimaging data converge with this conclusion, indicating distinct neural activity patterns depending on whether or not memory task-demands exceed this limit. STM for verbal information within that capacity invokes focal prefrontal cortical activation that increases with memory load. STM for verbal information exceeding that capacity invokes widespread prefrontal activation in regions associated with executive and attentional processes that may mediate chunking processes (...)
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  4. Steven A. Hecht & Todd K. Shackelford (2001). Pure Short-Term Memory Capacity has Implications for Understanding Individual Differences in Math Skills. Behavioral and Brain Sciences 24 (1):124-125.score: 120.0
    Future work is needed to establish that pure short-term memory is a coherent individual difference attribute that is separable from traditional compound short-term memory measures. Psychometric support for latent pure short-term memory capacity will provide an important starting point for future fine-grained analyses of the intrinsic factors that influence individual differences in math skills.
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  5. Rosaleen A. McCarthy & E. K. Warrington (1999). Backtracking? Rehearsing and Replaying Some Old Arguments About Short-Term Memory. Behavioral and Brain Sciences 22 (1):107-108.score: 120.0
    We discuss the role of short-term auditory verbal storage within a working memory system. Data from single case studies of patients with left parietal lesions and selective impairment of memory span are discussed in order to address the question of the functions of short-term memory in language processing. The backup resource of auditory verbal short-term memory is required for those tasks that necessitate backtracking in order to integrate a verbal message within a developing (...)
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  6. Steve Majerus, Martial Van der Linden, Fabienne Collette & Eric Salmon (2003). Does Sustained ERP Activity in Posterior Lexico-Semantic Processing Areas During Short-Term Memory Tasks Only Reflect Activated Long-Term Memory? Behavioral and Brain Sciences 26 (6):746-747.score: 120.0
    We challenge Ruchkin et al.'s claim in reducing short-term memory (STM) to the active part of long-term memory (LTM), by showing that their data cannot rule out the possibility that activation of posterior brain regions could also reflect the contribution of a verbal STM buffer.
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  7. Emmanuel M. Pothos & Patrick Juola (2001). Linguistic Structure and Short Term Memory. Behavioral and Brain Sciences 24 (1):138-139.score: 120.0
    We provide additional support for Cowan's claim that short term memory (STM) involves a range of 3–5 tokens, on the basis of language correlational analyses. If language is at least partly learned, linguistic dependency structure should reflect properties of the cognitive components mediating learning; one such component is STM. In this view, the range over which statistical regularity extends in ordinary text would be suggestive of STM span. Our analyses of eight languages are consistent with STM span being (...)
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  8. Werner X. Schneider, Heiner Deubel & Maria-Barbara Wesenick (2001). Characterizing Chunks in Visual Short-Term Memory: Not More Than One Feature Per Dimension? Behavioral and Brain Sciences 24 (1):144-145.score: 120.0
    Cowan defines a chunk as “a collection of concepts that have strong associations to one another and much weaker associations to other chunks currently in use.” This definition does not impose any constraints on the nature and number of elements that can be bound into a chunk. We present an experiment to demonstrate that such limitations exist for visual short-term memory, and that their analysis may lead to important insights into properties of visual memory.
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  9. Lester Ingber (2000). Statistical Mechanics of Neocortical Interactions: EEG Eigenfunctions of Short-Term Memory. Behavioral and Brain Sciences 23 (3):403-405.score: 120.0
    This commentary focuses on how bottom-up neocortical models can be developed into eigenfunction expansions of probability distributions appropriate to describe short-term memory in the context of scalp EEG. The mathematics of eigenfunctions are similar to the top-down eigenfunctions developed by Nunez, despite different physical manifestations. The bottom-up eigenfunctions are at the local mesocolumnar scale, whereas the top-down eigenfunctions are at the global regional scale. Our respective approaches have regions of substantial overlap, and future studies may expand top-down eigenfunctions (...)
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  10. Murray T. Maybery, Fabrice B. R. Parmentier & Peter J. Clissa (2003). Retention of Order and the Binding of Verbal and Spatial Information in Short-Term Memory: Constraints for Proceduralist Accounts. Behavioral and Brain Sciences 26 (6):748-748.score: 117.0
    Consistent with Ruchkin and colleagues' proceduralist account, recent research on grouping and verbal-spatial binding in immediate memory shows continuity across short- and long-term retention, and activation of classes of information extending beyond those typically allowed in modular models. However, Ruchkin et al.'s account lacks well-specified mechanisms for the retention of serial order, binding, and the control of activation through attention.
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  11. Giuseppe Vallar (2003). The Short-Term/Long-Term Memory Distinction: Back to the Past? Behavioral and Brain Sciences 26 (6):757-758.score: 117.0
    The view that short-term memory should be conceived of as being a process based on the activation of long-term memory is inconsistent with neuropsychological evidence. Data from brain-damaged patients, showing specific patterns of impairment, are compatible with a vision of memory as a multiple-component system, whose different aspects, in neurologically unimpaired subjects, show a high degree of interaction.
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  12. Elinor McKone (2001). Capacity Limits in Continuous Old-New Recognition and in Short-Term Implicit Memory. Behavioral and Brain Sciences 24 (1):130-131.score: 116.0
    Using explicit memory measures, Cowan predicts a new circumstance in which the central capacity limit of 4 chunks should obtain. Supporting results for such an experiment, using continuous old-new recognition, are described. With implicit memory measures, Cowan assumes that short-term repetition priming reflects the central capacity limit. I argue that this phenomenon instead reflects limits within individual perceptual processing modules.
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  13. Bill Faw (2003). Pre-Frontal Executive Committee for Perception, Working Memory, Attention, Long-Term Memory, Motor Control, and Thinking: A Tutorial Review. Consciousness and Cognition 12 (1):83-139.score: 102.0
  14. Uljana Feest (2011). Remembering (Short-Term) Memory: Oscillations of an Epistemic Thing. Erkenntnis 75 (3):391-411.score: 93.0
    This paper provides an interpretation of Hans-Jörg Rheinberger’s notions of epistemic things and historical epistemology . I argue that Rheinberger’s approach articulates a unique contribution to current debates about integrated HPS, and I propose some modifications and extensions of this contribution. Drawing on examples from memory research, I show that Rheinberger is right to highlight a particular feature of many objects of empirical research (“epistemic things”)—especially in the contexts of exploratory experimentation—namely our lack of knowledge about them. I argue (...)
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  15. David J. Murray (2002). The SOC Framework and Short-Term Memory. Behavioral and Brain Sciences 25 (3):347-348.score: 93.0
    Using a particular formula for quantifying the effortlessness that Perruchet & Vinter suggest accompanies the detection of repetition among a set of representations concurrently in consciousness, it is shown that both the Sternberg function and the Cavanagh function, associated with immediate probed recognition tasks and memory span tasks, can be predicted.
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  16. W. A. Phillips (1974). On the Distinction Between Sensory Storage and Visual Short-Term Memory. Perception and Psychophysics 16:283-90.score: 90.0
  17. R. W. Frick (1987). A Dissociation of Conscious Visual Imagery and Visual Short-Term Memory. Neuropsychologia 25:707-12.score: 90.0
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  18. Julia Fisher, E. Hirshman, T. HenThorn, J. Arndt & A. PAssannante (2006). Midazolam Amnesia and Short-Term/Working Memory Processes. Consciousness and Cognition 15 (1):54-63.score: 87.0
  19. Anthony G. Greenwald, R. L. Abrams, Lionel Naccache & Stanislas Dehaene (2003). Long-Term Semantic Memory Versus Contextual Memory in Unconscious Number Processing. Journal of Experimental Psychology 29 (2):235-247.score: 76.0
    Subjects classified visible 2-digit numbers as larger or smaller than 55. Target numbers were preceded by masked 2-digit primes that were either congruent (same relation to 55) or incongruent. Experiments 1 and 2 showed prime congruency effects for stimuli never included in the set of classified visible targets, indicating subliminal priming based on long-term semantic memory. Experiments 2 and 3 went further to demonstrate paradoxical unconscious priming effects resulting from task context. For example, after repeated practice classifying 73 (...)
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  20. Stephen Grossberg (2003). From Working Memory to Long-Term Memory and Back: Linked but Distinct. Behavioral and Brain Sciences 26 (6):737-738.score: 72.0
    Neural models have proposed how short-term memory (STM) storage in working memory and long-term memory (LTM) storage and recall are linked and interact, but are realized by different mechanisms that obey different laws. The authors' data can be understood in the light of these models, which suggest that the authors may have gone too far in obscuring the differences between these processes.
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  21. Daniel S. Ruchkin, Jordan Grafman, Katherine Cameron & Rita S. Berndt (2003). Working Memory Retention Systems: A State of Activated Long-Term Memory. Behavioral and Brain Sciences 26 (6):709-728.score: 72.0
    High temporal resolution event-related brain potential and electroencephalographic coherence studies of the neural substrate of short-term storage in working memory indicate that the sustained coactivation of both prefrontal cortex and the posterior cortical systems that participate in the initial perception and comprehension of the retained information are involved in its storage. These studies further show that short-term storage mechanisms involve an increase in neural synchrony between prefrontal cortex and posterior cortex and the enhanced activation of long-term (...)
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  22. Wolfgang Klimesch & Bärbel Schack (2003). Activation of Long-Term Memory by Alpha Oscillations in a Working-Memory Task? Behavioral and Brain Sciences 26 (6):743-743.score: 72.0
    We focus on the functional specificity of theta and alpha oscillations and show that theta is related to working memory, whereas alpha is related to semantic long-term memory. Recent studies, however, indicate that alpha oscillations also play an important role during short-term memory retention and retrieval. This latter finding provides support for the basic hypothesis suggested by Ruchkin et al.
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  23. William A. Phillips (2003). The Short-Term Dynamics Within a Network of Connections is Creative. Behavioral and Brain Sciences 26 (6):752-753.score: 72.0
    Although visual long-term memory (VLTM) and visual short-term memory (VSTM) can be distinguished from each other (and from visual sensory storage [SS]), they are embodied within the same modality-specific brain regions, but in very different ways: VLTM as patterns of connectivity and VSTM as patterns of activity. Perception and VSTM do not “activate” VLTM. They use VLTM to create novel patterns of activity relevant to novel circumstances.
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  24. Jackie Andrade (2001). The Contribution of Working Memory to Conscious Experience. In Jackie Andrade (ed.), Working Memory in Perspective. Psychology Press.score: 72.0
  25. James S. Nairne & Ian Neath (2001). Long-Term Memory Span. Behavioral and Brain Sciences 24 (1):134-135.score: 71.0
    Cowan assumes that chunk-based capacity limits are synonymous with the essence of a “specialized STM mechanism.” In a single experiment, we measured the capacity, or span, of long-term memory and found that it, too, corresponds roughly to the magical number 4. The results imply that a chunk-based capacity limit is not a signature characteristic of remembering over the short-term.
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  26. Frank Rösler & Martin Heil (2003). Working Memory as a State of Activated Long-Term Memory: A Plausible Theory, but Other Data Provide More Compelling Evidence. Behavioral and Brain Sciences 26 (6):754-755.score: 71.0
    The identity of working-memory and long-term memory representations follows from many lines of evidence. However, the data provided by Ruchkin et al. are hardly compelling, as they make unproved assumptions about hypothetical generators. We cite studies from our lab in which congruent slow-wave topographies were found for short-term and long-term memory tasks, strongly suggesting that both activate identical cell assemblies.
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  27. Bernard J. Baars & Stan Franklin (2003). How Conscious Experience and Working Memory Interact. Trends in Cognitive Sciences 7 (4):166-172.score: 69.0
  28. Arthur I. Miller (2007). Unconscious Thought, Intuition, and Visual Imagery: A Critique of "Working Memory, Cerebellum, and Creativity". Creativity Research Journal 19 (1):47-48.score: 69.0
  29. Michael F. Bunting & Nelson Cowan (2005). Working Memory and Flexibility in Awareness and Attention. Psychological Research/Psychologische Forschung 69 (5):412-419.score: 69.0
  30. Susanne Ferber & Stephen M. Emrich (2007). Maintaining the Ties That Bind: The Role of an Intermediate Visual Memory Store in the Persistence of Awareness. Cognitive Neuropsychology 24 (2):187-210.score: 69.0
  31. David Soto & Glyn W. Humphreys (2006). Seeing the Content of the Mind: Enhanced Awareness Through Working Memory in Patients with Visual Extinction. Proceedings of the National Academy of Sciences of the United States of America 103 (12):4789-4792.score: 69.0
  32. Ran R. Hassin (2005). Nonconscious Control and Implicit Working Memory. In Ran R. Hassin, James S. Uleman & John A. Bargh (eds.), The New Unconscious. Oxford Series in Social Cognition and Social Neuroscience. Oxford University Press.score: 69.0
  33. Naoyuki Osaka (2002). Neural Correlates of Visual Working Memory for Motion. In Kunio Yasue, Marj Jibu & Tarcisio Della Senta (eds.), No Matter, Never Mind: Proceedings of Toward a Science of Consciousness: Fundamental Approaches (Tokyo '99). John Benjamins.score: 69.0
  34. Andreas K. Engel & Wolf Singer (2001). Temporal Binding and the Neural Correlates of Sensory Awareness. Trends in Cognitive Sciences 5 (1):16-25.score: 63.0
    Theories of binding have recently come into the focus of the consciousness debate. In this review, we discuss the potential relevance of temporal binding mechanisms for sensory awareness. Specifically, we suggest that neural synchrony with a precision in the millisecond range may be crucial for conscious processing, and may be involved in arousal, perceptual integration, attentional selection and working memory. Recent evidence from both animal and human studies demonstrates that specific changes in neuronal synchrony occur during all of these (...)
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  35. Stan Klein (2013). Making the Case That Episodic Recollection is Attributable to Operations Occurring at Retrieval Rather Than to Content Stored in a Dedicated Subsystem of Long-Term Memory. Frontiers in Behavioral Neuroscience 7 (3):1-14.score: 62.0
    Episodic memory often is conceptualized as a uniquely human system of long-term memory that makes available knowledge accompanied by the temporal and spatial context in which that knowledge was acquired. Retrieval from episodic memory entails a form of first–person subjectivity called autonoetic consciousness that provides a sense that a recollection was something that took place in the experiencer’s personal past. In this paper I expand on this definition of episodic memory. Specifically, I suggest that (a) (...)
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  36. Bernard J. Baars (2002). The Conscious Access Hypothesis: Origins and Recent Evidence. Trends in Cognitive Sciences 6 (1):47-52.score: 60.0
  37. Sam M. Doesburg, Keiichi Kitajo & Lawrence M. Ward (2005). Increased Gamma-Band Synchrony Precedes Switching of Conscious Perceptual Objects in Binocular Rivalry. Neuroreport 16 (11):1139-1142.score: 60.0
  38. Tiago V. Maia & Axel Cleeremans (2005). Consciousness: Converging Insights From Connectionist Modeling and Neuroscience. Trends in Cognitive Sciences 9 (8):397-404.score: 60.0
  39. David LaBerge (2006). Apical Dendrite Activity in Cognition and Consciousness. Consciousness and Cognition 15 (2):235-257.score: 60.0
  40. Ravi K. Kurup & Parameswara A. Kurup (2003). A Hypothalamic Digoxin-Mediated Model for Conscious and Subliminal Perception. International Journal of Neuroscience 113 (6):815-820.score: 60.0
  41. K. Imanaka & Brad Abernethy (2000). Distance-Location Interference in Movement Reproduction: An Interaction Between Conscious and Unconscious Processing? In Yves Rossetti & Antti Revonsuo (eds.), Beyond Dissociation: Interaction Between Dissociated Implicit and Explicit Processing. John Benjamins.score: 60.0
  42. Marcel Kinsbourne (2005). A Continuum of Self-Consciousness That Emerges in Phylogeny and Ontogeny. In Herbert S. Terrace & Janet Metcalfe (eds.), The Missing Link in Cognition: Origins of Self-Reflective Consciousness. Oxford University Press.score: 60.0
  43. Catherine Tallon-Baudry (2003). Oscillatory Synchrony as a Signature for the Unity of Visual Experience in Humans. In Axel Cleeremans (ed.), The Unity of Consciousness. Oxford University Press.score: 60.0
     
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  44. Joaquín M. Fuster (2003). More Than Working Memory Rides on Long-Term Memory. Behavioral and Brain Sciences 26 (6):737-737.score: 56.0
    Single-unit data from the cortex of monkeys performing working-memory tasks support the main point of the target article. Those data, however, also indicate that the activation of long-term memory is essential to the processing of all cognitive functions. The activation of cortical long-term memory networks is a key neural mechanism in attention (working memory is a form thereof), perception, memory acquisition and retrieval, intelligence, and language.
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  45. Robert H. Logie & Sergio Della Sala (2003). Working Memory as a Mental Workspace: Why Activated Long-Term Memory is Not Enough. Behavioral and Brain Sciences 26 (6):745-746.score: 56.0
    Working-memory retention as activated long-term memory fails to capture orchestrated processing and storage, the hallmark of the concept of working memory. The event-related potential (ERP) data are compatible with working memory as a mental workspace that holds and manipulates information on line, which is distinct from long-term memory, and deals with the products of activated traces from stored knowledge.
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  46. Michele K. Langowski & Ana S. Iltis (2011). Global Health Needs and the Short-Term Medical Volunteer: Ethical Considerations. HEC Forum 23 (2):71-78.score: 56.0
    Global Health Needs and the Short-Term Medical Volunteer: Ethical Considerations Content Type Journal Article Pages 71-78 DOI 10.1007/s10730-011-9158-5 Authors Michele K. Langowski, Albert Gnaegi Center for Health Care Ethics, Salus Center, Saint Louis University, 3545 Lafayette, 5th Floor, St. Louis, MO 63104-1314, USA Ana S. Iltis, Department of Philosophy and Center for Bioethics, Health and Society, Wake Forest University, P.O. Box 7332, Winston-Salem, NC 27109, USA Journal HEC Forum Online ISSN 1572-8498 Print ISSN 0956-2737 Journal Volume Volume 23 Journal (...)
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  47. Jennifer D. Ryan & Neal J. Cohen (2003). The Contribution of Long-Term Memory and the Role of Frontal-Lobe Systems in on-Line Processing. Behavioral and Brain Sciences 26 (6):756-756.score: 56.0
    Ruchkin et al. ascribe a pivotal role to long-term memory representations and binding within working memory. Here we focus on the interaction of working memory and long-term memory in supporting on-line representations of experience available to guide on-going processing, and we distinguish the role of frontal-lobe systems from what the hippocampus contributes to relational long-term memory binding.
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  48. Matthew DeCamp (2011). Ethical Review of Global Short-Term Medical Volunteerism. HEC Forum 23 (2):91-103.score: 56.0
    Global short-term medical volunteerism is growing, and properly conducted, is a tool in the fight for greater global health equity. It is intrinsically ethical (i.e., it involves ethics at every step) and depends upon ethical conduct for its success. At present, ethical guidelines remain in their infancy, which presents a unique opportunity. This paper presents a set of basic ethical principles, building on prior work in this area and previously developed guidelines for international clinical research. The content of these (...)
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  49. John T. Manning & Alex R. Gage (2000). Low Fluctuating Asymmetry (FA) and Short-Term Benefits in Fertility? Behavioral and Brain Sciences 23 (4):610-611.score: 56.0
    Preference for partners with low fluctuating asymmetry (FA) may produce “good gene” benefits. However, Gangestad & Simpson's analysis does not exclude immediate benefits of fertility. Low FA is related to fertility in men and women. Short-term changes in FA are correlated with fertility in women. It is not known whether temporal fluctuations in the FA of men are related to short-term fertility status.
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  50. Sergio Morra (2003). Developmental Evidence for Working Memory as Activated Long-Term Memory. Behavioral and Brain Sciences 26 (6):750-750.score: 56.0
    There is remarkable agreement between Ruchkin et al.'s psychophysiological views and my own model, based on developmental-experimental evidence, of working memory as activated long-term memory (LTM). I construe subvocal rehearsal as an operative scheme that maintains order information and demands attentional resources. Encoding and retrieving operations also demand attention. Another share of resources is used for keeping activated specific LTM representations.
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  51. Lynn Carol Miller, William C. Pedersen, Allison R. Johnson & Anila D. Putcha (2000). For the Short-Term: Are Women Just Looking for a Few Pair of Genes? Behavioral and Brain Sciences 23 (4):614-615.score: 56.0
    Although we find Gangestad & Simpson's argument intriguing, we question some of its underlying assumptions, including: (1) that fluctuating asymmetry (FA) is consistently heritable; (2) that symmetry is driving the effects; (3) that use of parametric tests with FA is appropriate; and (4) that a short-term mating strategy produces more offspring than a long-term strategy.
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  52. Bradley A. Striebig, Tyler Jantzen & Katherine Rowden (2006). Ethical Considerations of the Short-Term and Long-Term Health Impacts, Costs, and Educational Value of Sustainable Development Projects. Science and Engineering Ethics 12 (2).score: 56.0
    There are over 800 seventh to tenth grade students at the College d’Enseignment Generale (CEG) School in Azové, Benin. Like most children in the developing world, these students lack access to clean water and basic sanitation facilities. These students suffer from parasitic infection and health ailments which could be directly offset with short term aid to supply water and medical aid. Promoting proper sanitation and providing the technology to implement water and wastewater treatment in the community will decrease childhood (...)
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  53. S. Dehaene, A. G. Greenwald, R. L. Abrams & L. Naccache (2003). Long-Term Semantic Memory Versus Contextual Memory in Unconscious Number Processing. Journal of Experimental Psychology 29 (2):235-247.score: 48.0
    Subjects classified visible 2-digit numbers as larger or smaller than 55. Target numbers were preceded by masked 2-digit primes that were either congruent (same relation to 55) or incongruent. Experiments 1 and 2 showed prime congruency effects for stimuli never included in the set of classified visible targets, indicating subliminal priming based on long-term semantic memory. Experiments 2 and 3 went further to demonstrate paradoxical unconscious priming effects resulting from task context. For example, after repeated practice classifying 73 (...)
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  54. Anne P. DePrince, Carolyn B. Allard, Hannah Oh & Jennifer J. Freyd (2004). What's in a Name for Memory Errors? Implications and Ethical Issues Arising From the Use of the Term "False Memory" for Errors in Memory for Details. Ethics and Behavior 14 (3):201 – 233.score: 48.0
    The term "false memories" has been used to refer to suggestibility experiments in which whole events are apparently confabulated and in media accounts of contested memories of childhood abuse. Since 1992 psychologists have increasingly used the term "false memory" when discussing memory errors for details, such as specific words within word lists. Use of the term to refer to errors in details is a shift in language away from other terms used historically (e.g., "memory (...)
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  55. Penelope Rowlatt (2009). Consciousness and Memory. Journal of Consciousness Studies 16 (5):68-78.score: 45.0
    Defining consciousness along the lines of Nagel, an organism has consciousness iff there is something it is like to be that organism, I relate three types of consciousness (phenomenal, access and reflexive) to the three types of short-term memory (sensory memories, short-term working memory and the central executive). The suggestion is that these short-term memory stores may be a key feature of consciousness.
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  56. Jonathan K. Foster (2003). Thoughts From the Long-Term Memory Chair. Behavioral and Brain Sciences 26 (6):734-735.score: 45.0
    With reference to Ruchkins et al.'s framework, this commentary briefly considers the history of working memory, and whether, heuristically, this is a useful concept. A neuropsychologically motivated critique is offered, specifically with regard to the recent trend for working-memory researchers to conceptualise this capacity more as a process than as a set of distinct task-specific stores.
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  57. John Sweller (1998). Can We Measure Working Memory Without Contamination From Knowledge Held in Long-Term Memory? Behavioral and Brain Sciences 21 (6):845-846.score: 45.0
    The metric devised by Halford, Wilson & Phillips may have considerable potential in distinguishing between the working memory demands of different tasks but may be less effective in distinguishing working memory capacity between individuals. Despite the strengths of the metric, determining whether an effect is caused by relational complexity or by differential levels of expertise is currently problematic.
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  58. Dorcas M. Kamuya, Sally J. Theobald, Patrick K. Munywoki, Dorothy Koech, Wenzel P. Geissler & Sassy C. Molyneux (2013). Evolving Friendships and Shifting Ethical Dilemmas: Fieldworkers' Experiences in a Short Term Community Based Study in Kenya. Developing World Bioethics 13 (1):1-9.score: 45.0
    Fieldworkers (FWs) are community members employed by research teams to support access to participants, address language barriers, and advise on culturally appropriate research conduct. The critical role that FWs play in studies, and the range of practical and ethical dilemmas associated with their involvement, is increasingly recognised. In this paper, we draw on qualitative observation and interview data collected alongside a six month basic science study which involved a team of FWs regularly visiting 47 participating households in their homes. The (...)
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  59. Klaus G. Reymann (1997). As in Long-Term Memory, LTP is Consolidated by Reinforcers. Behavioral and Brain Sciences 20 (4):627-628.score: 45.0
    Recent evidence from our lab indicates that LTP shares an important property with memory consolidation: it is consolidated by natural reinforcement. Nevertheless, the hypothesis, that LTP-like mechanisms or other forms of enhanced synaptic efficacy are basic elements in learning is not unequivocally supported. Skepticism aside, LTP is an accessible experimental model that is optimally equipped for the investigation of the cellular and molecular machinery involved in synaptic weight changes.
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  60. Philip M. Rosoff (2012). Unpredictable Drug Shortages: An Ethical Framework for Short-Term Rationing in Hospitals. American Journal of Bioethics 12 (1):1 - 9.score: 42.0
    Periodic and unexpected shortages of drugs, biologics, and even medical devices have become commonplace in the United States. When shortages occur, hospitals and clinics need to decide how to ration their available stock. When such situations arise, institutions can choose from several different allocation schemes, such as first-come, first-served, a lottery, or a more rational and calculated approach. While the first two approaches sound reasonable at first glance, there are a number of problems associated with them, including the inability to (...)
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  61. Nick Bostrom, Cortical Integration: Possible Solutions to the Binding and Linking Problems in Perception, Reasoning and Long Term Memory.score: 42.0
    The problem of cortical integration is described and various proposed solutions, including grandmother cells, cell assemblies, feed-forward structures, RAAM and synchronization, are reviewed. One method, involving complex attractors, that has received little attention in the literature, is explained and developed. I call this binding through annexation. A simulation study is then presented which suggests ways in which complex attractors could underlie our capacity to reason. The paper ends with a discussion of the efficiency and biological plausibility of the proposals as (...)
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  62. Robin Pierce (2009). Considering the Long Term in the Short Term Use of Fmri in the Classroom. American Journal of Bioethics 9 (1):33 – 35.score: 42.0
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  63. Matthew DeCamp (2007). Scrutinizing Global Short-Term Medical Outreach. Hastings Center Report 37 (6):21-23.score: 42.0
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  64. L. Cahill (2004). The Influence of Sex Versus Sex-Related Traits on Long-Term Memory for Gist and Detail From an Emotional Story. Consciousness and Cognition 13 (2):391-400.score: 42.0
  65. William F. Brewer & John R. Pani (1996). Reports of Mental Imagery in Retrieval From Long-Term Memory. Consciousness and Cognition 5 (3):265-287.score: 42.0
  66. Kristy A. Nielson & Mitchell A. Meltzer (2009). Modulation of Long-Term Memory by Arousal in Alexithymia: The Role of Interpretation. Consciousness and Cognition 18 (3):786-793.score: 42.0
  67. A. Newman (2006). Authorship of Research Papers: Ethical and Professional Issues for Short-Term Researchers. Journal of Medical Ethics 32 (7):420-423.score: 42.0
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  68. Alexander A. Fingelkurts, Andrew A. Fingelkurts, Sergio Bagnato, Cristina Boccagni & Giuseppe Galardi (2013). The Value of Spontaneous EEG Oscillations in Distinguishing Patients in Vegetative and Minimally Conscious States. In Eror Basar & et all (eds.), Application of Brain Oscillations in Neuropsychiatric Diseases. Supplements to Clinical Neurophysiology. Elsevier.score: 42.0
    Objective: The value of spontaneous EEG oscillations in distinguishing patients in vegetative and minimally conscious states was studied. Methods: We quantified dynamic repertoire of EEG oscillations in resting condition with closed eyes in patients in vegetative and minimally conscious states (VS and MCS). The exact composition of EEG oscillations was assessed by the probability-classification analysis of short-term EEG spectral patterns. Results: The probability of delta, theta and slow-alpha oscillations occurrence was smaller for patients in MCS than for VS. Additionally, (...)
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  69. R. Asgary & E. Junck (forthcoming). New Trends of Short-Term Humanitarian Medical Volunteerism: Professional and Ethical Considerations. Journal of Medical Ethics.score: 42.0
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  70. Jeremy Pierce (forthcoming). A Realist Metaphysics of Race: A Context-Sensitive, Short-Term Retentionist, Long-Term Revisionist Approach. Rowman & Littlefield/Lexington Books.score: 42.0
  71. Henry Markovits, Celine Doyon & Michael Simoneau (2002). Individual Differences in Working Memory and Conditional Reasoning with Concrete and Abstract Content. Thinking and Reasoning 8 (2):97 – 107.score: 39.0
    This study examined the hypothesis that conditional reasoning involves visual short-term memory resources (Johnson-Laird, 1985). A total of 147 university students were given measures of verbal and visual short-term memory capacity and a series of concrete and abstract conditional reasoning problems. Results indicate that there is a positive correlation between verbal working memory capacity and reasoning with both concrete and abstract premises. A positive correlation was also obtained between visual working memory capacity and reasoning (...)
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  72. Daniel S. Ruchkin, Jordan Grafman, Katherine Cameron & Rita S. Berndt (2003). Working Memory: Unemployed but Still Doing Day Labor. Behavioral and Brain Sciences 26 (6):760-769.score: 39.0
    The goal of our target article is to establish that electrophysiological data constrain models of short-term memory retention operations to schemes in which activated long-term memory is its representational basis. The temporary stores correspond to neural circuits involved in the perception and subsequent processing of the relevant information, and do not involve specialized neural circuits dedicated to the temporary holding of information outside of those embedded in long-term memory. The commentaries ranged from general agreement (...)
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  73. Jerwen Jou (2001). The Magic Number Four: Can It Explain Sternberg's Serial Memory Scan Data? Behavioral and Brain Sciences 24 (1):126-127.score: 39.0
    Cowan's concept of a pure short-term memory (STM) capacity limit is equivalent to that of memory subitizing. However, a robust phenomenon well known in the Sternberg paradigm, that is, the linear increase of RT as a function of memory set size is not consistent with this concept. Cowan's STM capacity theory will remain incomplete until it can account for this phenomenon.
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  74. Michael D. Patterson & Bart Rypma (2003). Will the Unitary View Survive the Short- and Long-Term? Behavioral and Brain Sciences 26 (6):751-752.score: 39.0
    In this commentary, we focus on four points. First, we discuss the assertion that the unitary model explains dissociations that implicate multiple systems. Second, the distinct nature of information utilized in immediate- and delayed-recall supports the distinct memory systems view. Third, the variable nature of capacity limits corroborates this view. Finally, we review event-related fMRI results that suggest support for multiple systems.
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  75. Jonathan K. Foster (2008). Memory: A Very Short Introduction. OUP Oxford.score: 39.0
    Why do we remember events from our childhood as if they happened yesterday, but not what we did last week? Why does our memory seem to work well sometimes and not others? What happens when it goes wrong? Can memory be improved or manipulated, by psychological techniques or even 'brain implants'? How does memory grow and change as we age? And what of so-called 'recovered' memories? -/- This book brings together the latest research in neuroscience and psychology, (...)
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  76. John N. Towse (2001). Memory Limits: “Give Us an Answer!”. Behavioral and Brain Sciences 24 (1):150-151.score: 39.0
    Cowan has written a meticulous and thought-provoking review of the literature on short-term memory. However, reflections on one area of evidence, that of working memory span, shows the extent to which the research debate can be circumscribed by choice of experimental paradigms.
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  77. Matthew Shapiro & Eric Hargreaves (1997). Long Term Potentiation: Attending to Levels of Organization of Learning and Memory Mechanisms. Behavioral and Brain Sciences 20 (4):631-632.score: 39.0
    Shors & Matzel set up a straw man, that LTP is a memory storage mechanism, and knock him down without due consideration of the important relations among different levels of organization and analysis regarding LTP, learning, and memory. Assessing these relationships requires analysis and hypotheses linking specific brain regions, neural circuits, plasticity mechanisms, and task demands. The issue addressed by the authors is important, but their analysis is off target.
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  78. John A. Michon (1975). Time Experience and Memory Processes. In J. T. Fraser & Nathaniel M. Lawrence (eds.), The Study of Time Ii. Springer-Verlag.score: 39.0
    The experience of time, and more particularly of duration, has been studied rather separately from its functional fundament: the memory process. Yet, in the past few years some rather intriguing patterns of connection have emerged. Especially the effect of the usual distinction between immediate memory (IM), short term memory (STM) and long term memory (LTM) (Shiffrin and Atkinson 1969; Norman 1970) seems to provide some conceptual cement to link the two fields: time and (...). (shrink)
     
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  79. Edmund T. Rolls (2007). Memory, Attention, and Decision-Making: A Unifying Computational Neuroscience Approach. OUP Oxford.score: 39.0
    Memory, attention, and decision-making are three major areas of psychology. They are frequently studied in isolation, and using a range of models to understand them. This book brings a unified approach to understanding these three processes. It shows how these fundamental functions for cognitive neuroscience can be understood in a common and unifying computational neuroscience framework. This framework links empirical research on brain function from neurophysiology, functional neuroimaging, and the effects of brain damage, to a description of how neural (...)
     
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  80. P. Graf & B. Uttl (2001). Prospective Memory: A New Focus for Research. Consciousness and Cognition 10 (4):437-450.score: 38.0
    Prospective memory is required for many aspects of everyday cognition, its breakdown may be as debilitating as impairments in retrospective memory, and yet, the former has received relatively little attention by memory researchers. This article outlines a strategy for changing the fortunes of prospective memory, for guiding new research to shore up the claim that prospective memory is a distinct aspect of cognition, and to obtain evidence for clear performance dissociations between prospective memory and (...)
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  81. Christian Abry, Marc Sato, Jean-Luc Schwartz, Hélène Loevenbruck & Marie-Agnès Cathiard (2003). Attention-Based Maintenance of Speech Forms in Memory: The Case of Verbal Transformations. Behavioral and Brain Sciences 26 (6):728-729.score: 38.0
    One of the fundamental questions raised by Ruchkin, Grafman, Cameron, and Berndt's (Ruchkin et al.'s) interpretation of no distinct specialized neural networks for short-term storage buffers and long-term memory systems, is that of the link between perception and memory processes. In this framework, we take the opportunity in this commentary to discuss a specific working memory task involving percept formation, temporary retention, auditory imagery, and the attention-based maintenance of information, that is, the verbal transformation effect.
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  82. John Bickle (2002). Concepts Structured Through Reduction: A Structuralist Resource Illuminates the Consolidation – Long-Term Potentiation (Ltp) Link. Synthese 130 (1):123 - 133.score: 38.0
    The structuralist program has developed a useful metascientific resource: ontological reductive links (ORLs) between the constituents of the potential models of reduced and reducing theories. This resource was developed initially to overcome an objection to structuralist ``global'' accounts of the intertheoretic reduction relation. But it also illuminates the way that concepts at a higher level of scientific investigation (e.g., cognitive psychology) become ``structured through reduction'' to lower-level investigations (e.g., cellular/molecular neuroscience). After (briefly) explaining this structuralist background, I demonstrate how this (...)
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  83. K. J. Gilhooly, V. Wynn, L. H. Phillips, R. H. Logie & S. Della Sala (2002). Visuo-Spatial and Verbal Working Memory in the Five-Disc Tower of London Task: An Individual Differences Approach. Thinking and Reasoning 8 (3):165 – 178.score: 38.0
    This paper reports a study of the roles of visuo-spatial and verbal working memory capacities in solving a planning task - the five-disc Tower of London (TOL) task. An individual differences approach was taken. Sixty adult participants were tested on 20 TOL tasks of varying difficulty. Total moves over the 20 TOL tasks was taken as a measure of performance. Participants were also assessed on measures of fluid intelligence (Raven's matrices), verbal short-term storage (Digit span), verbal working (...) span (Silly Sentence span), visuo-spatial short-term storage (Visual Pattern span and Corsi Block span), visuo-spatial working memory (Corsi Distance Estimation), visuo-spatial processing speed (Manikin test), and verbal speed (Rehearsal speed). Exploratory factor analysis using an oblique rotation method revealed three factors which were interpreted as (1) a visuo-spatial working memory factor, (2) an age-speed factor, and (3) a verbal working memory factor. The visuo-spatial and verbal factors were only moderately correlated. Performance on the TOL task loaded on the visuo-spatial factor but did not load on the other factors. It is concluded that the predominant goal-selection strategy adopted in solving the TOL relies on visuo-spatial working memory capacity and particularly involves the active ''inner scribe'' spatial rehearsal mechanism. These correlational analyses confirm and extend results previously obtained by use of dual task methods, (Phillips, Wynn, Gilhooly, Della Sala, & Logie, 1999). (shrink)
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  84. Han Lee & Gregory V. Simpson (2005). Phase Locking of Single Neuron Activity to Theta Oscillations During Working Memory in Monkey Extrastriate Visual Cortex. Neuron 45:147-156.score: 38.0
    activity” has been considered to play a major role in the short-term maintenance of memories. Many studies since then have provided support for this view and greatly advanced our knowledge of the effects of stimulus type and modality on delay activity and its temporal dynamics (Funahashi et al., 1993; Fuster et al., 2000; Romo et al., 1999). In humans, working memory has also been a subject of intense investigation using scalp and intracranial electroencephalography (EEG, iEEG) as well as (...)
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  85. Michael E. Young (2004). The Short- and Long-Term Consequences of Believing an Illusion. Behavioral and Brain Sciences 27 (5):677-678.score: 36.0
    The experience of free will has causal consequences, albeit not immediate ones. Although Wegner recognizes this, his model failed to incorporate this causal link. Is this experience central to “what makes us human”? A broad acceptance of Wegner's claim that free will is illusory has significant societal and religious consequences, therefore the threshold of evidence needs to be correspondingly high.
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  86. James K. Kroger (2003). Long-Term Memories, Features, and Novelty. Behavioral and Brain Sciences 26 (6):744-745.score: 34.0
    Ruchkin et al. make a strong claim about the neural substrates of active information. Some qualifications on that conclusion are: (1) Long-term memories and neural substrates activated for perception of information are not the same thing; (2) humans are capable of retaining novel information in working memory, which is not long-term memory; (3) the content of working memory, a dynamically bound representation, is a quantity above and beyond the long-term memories activated, or the activity (...)
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  87. John Bickle (2006). Reducing Mind to Molecular Pathways: Explicating the Reductionism Implicit in Current Cellular and Molecular Neuroscience. Synthese 151 (3):411-434.score: 31.0
    As opposed to the dismissive attitude toward reductionism that is popular in current philosophy of mind, a “ruthless reductionism” is alive and thriving in “molecular and cellular cognition”—a field of research within cellular and molecular neuroscience, the current mainstream of the discipline. Basic experimental practices and emerging results from this field imply that two common assertions by philosophers and cognitive scientists are false: (1) that we do not know much about how the brain works, and (2) that lower-level neuroscience cannot (...)
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  88. Katharina Henke, Valerie Treyer, Eva T. Nagy, Stefan Kneifel, Max Düsteler, Roger M. Nitsch & Alfred Buck (2003). Active Hippocampus During Nonconscious Memories. Consciousness and Cognition 12 (1):31-48.score: 31.0
  89. Hava T. Siegelmann (2003). Neural and Super-Turing Computing. Minds and Machines 13 (1):103-114.score: 30.0
    ``Neural computing'' is a research field based on perceiving the human brain as an information system. This system reads its input continuously via the different senses, encodes data into various biophysical variables such as membrane potentials or neural firing rates, stores information using different kinds of memories (e.g., short-term memory, long-term memory, associative memory), performs some operations called ``computation'', and outputs onto various channels, including motor control commands, decisions, thoughts, and feelings. We show a natural (...)
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  90. John Beeckmans (2007). Can Higher-Order Representation Theories Pass Scientific Muster? Journal of Consciousness Studies 14 (s 9-10):90-111.score: 30.0
    Higher-order representation (HOR) theories posit that the contents of lower-order brain states enter consciousness when tracked by a higher-order brain state. The nature of higher-order monitoring was examined in light of current scientific knowledge, primarily in experimental perceptual psychology. The most plausible candidate for higher-order state was found to be conceptual short-term memory (CSTM), a buffer memory intimately connected with a semantic engine operating in the medium of the language of thought (LOT). This combination meets many of (...)
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  91. Robyn Langdon, Martin Davies & Max Coltheart (2002). Understanding Minds and Understanding Communicated Meanings in Schizophrenia. Mind and Language 17 (1-2):68-104.score: 30.0
    Cognitive neuropsychology is that branch of cognitive psychology that investi- gates people with acquired or developmental disorders of cognition. The aim is to learn more about how cognitive systems normally operate or about how they are normally acquired by studying selective patterns of cognitive break- down after brain damage or selective dif?culties in acquiring particular cogni- tive abilities. In the early days of modern cognitive neuropsychology, research focused on rather basic cognitive abilities such as speech comprehension or production at the (...)
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  92. James Mensch, Imagination and Machine Intelligence.score: 30.0
    The question of the imagination is rather like the question Augustine raised with regard to the nature of time. We all seem to know what it involves, yet find it difficult to define. For Descartes, the imagination was simply our faculty for producing a mental image. He distinguished it from the understanding by noting that while the notion of a thousand sided figure was comprehensible—that is, was sufficiently clear and distinct to be differentiated from a thousand and one sided figure—the (...)
     
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  93. Martin Davies, Understanding Minds and Understanding Communicated Meanings in Schizophrenia.score: 30.0
    Cognitive neuropsychology is that branch of cognitive psychology that investigates people with acquired or developmental disorders of cognition. The aim is to learn more about how cognitive systems normally operate or about how they are normally acquired by studying selective patterns of cognitive breakdown after brain damage or selective difficulties in acquiring particular cognitive abilities. In the early days of modern cognitive neuropsychology, research focused on rather basic cognitive abilities such as speech comprehension or production at the single-word level, reading (...)
     
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  94. Alexander Grunewald (1999). Neurophysiology Indicates Cognitive Penetration of the Visual System. Behavioral and Brain Sciences 22 (3):379-380.score: 30.0
    Short-term memory, nonattentional task effects and nonspatial extraretinal representations in the visual system are signs of cognitive penetration. All of these have been found physiologically, arguing against the cognitive impenetrability of vision as a whole. Instead, parallel subcircuits in the brain, each subserving a different competency including sensory and cognitive (and in some cases motor) aspects, may have cognitively impenetrable components.
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  95. Graeme S. Halford, Steven Phillips & William H. Wilson (2001). Processing Capacity Limits Are Not Explained by Storage Limits. Behavioral and Brain Sciences 24 (1):123-124.score: 30.0
    Cowan's review shows that a short-term memory limit of four items is consistent with a wide range of phenomena in the field. However, he does not explain that limit, whereas an existing theory does offer an explanation for capacity limitations. Furthermore, processing capacity limits cannot be reduced to storage limits as Cowan claims.
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  96. D. Kahn, E. Pace-Schott & J. A. Hobson (2002). Emotion and Cognition: Feeling and Character Identification in Dreaming. Consciousness and Cognition 11 (1):34-50.score: 30.0
    This study investigated the relationship between dream emotion and dream character identification. Thirty-five subjects provided 320 dream reports and answers to questions on characters that appeared in their dreams. We found that emotions are almost always evoked by our dream characters and that they are often used as a basis for identifying them. We found that affection and joy were commonly associated with known characters and were used to identify them even when these emotional attributes were inconsistent with those of (...)
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  97. Hannu Tiitinen (2001). How to Interface Cognitive Psychology with Cognitive Neuroscience? Behavioral and Brain Sciences 24 (1):148-149.score: 30.0
    Cowan's analysis of human short-term memory (STM) and attention in terms of processing limits in the range of 4 items (or “chunks”) is discussed from the point of view of cognitive neuroscience. Although, Cowan already provides many important theoretical insights, we need to learn more about how to build further bridges between cognitive psychology and cognitive neuroscience.
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  98. Peter M. Milner (2001). Magical Attention. Behavioral and Brain Sciences 24 (1):131-131.score: 30.0
    Cowan postulates that the capacity of short-term memory is limited to the number of items to which attention can be simultaneously directed. Unfortunately, he endows attention with unexplained properties, such as being able to locate the most recent inputs to short-term memory, so his theory does little more than restate the data.
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  99. K. Anders Ericsson & Elizabeth P. Kirk (2001). The Search for Fixed Generalizable Limits of “Pure STM” Capacity: Problems with Theoretical Proposals Based on Independent Chunks. Behavioral and Brain Sciences 24 (1):120-121.score: 30.0
    Cowan's experimental techniques cannot constrain subject's recall of presented information to distinct independent chunks in short-term memory (STM). The encoding of associations in long-term memory contaminates recall of pure STM capacity. Even in task environments where the functional independence of chunks is convincingly demonstrated, individuals can increase the storage of independent chunks with deliberate practice – well above the magical number four.
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  100. Ole Jensen & John E. Lisman (2001). Dual Oscillations as the Physiological Basis for Capacity Limits. Behavioral and Brain Sciences 24 (1):126-126.score: 30.0
    A physiological model for short-term memory (STM) based on dual theta (5–10 Hz) and gamma (20–60 Hz) oscillation was proposed by Lisman and Idiart (1995). In this model a memory is represented by groups of neurons that fire in the same gamma cycle. According to this model, capacity is determined by the number of gamma cycles that occur within the slower theta cycle. We will discuss here the implications of recent reports on theta oscillations recorded in humans (...)
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