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  1. A Higher-Order Theory of Emotional Consciousness.Joseph LeDoux & Richard Brown - 2017 - Proceedings of the National Academy of Sciences of the United States of America 114 (10):E2016-E2025.
    Emotional states of consciousness, or what are typically called emotional feelings, are traditionally viewed as being innately programed in subcortical areas of the brain, and are often treated as different from cognitive states of consciousness, such as those related to the perception of external stimuli. We argue that conscious experiences, regardless of their content, arise from one system in the brain. On this view, what differs in emotional and non-emotional states is the kind of inputs that are processed by a (...)
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  • What memory is.Stan Klein - 2015 - WIREs Cognitive Science 6 (1):1-38.
    I argue that our current practice of ascribing the term “ memory ” to mental states and processes lacks epistemic warrant. Memory, according to the “received view”, is any state or process that results from the sequential stages of encoding, storage and retrieval. By these criteria, memory, or its footprint, can be seen in virtually every mental state we are capable of having. This, I argue, stretches the term to the breaking point. I draw on phenomenological, historical and conceptual considerations (...)
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  • Retention and transfer of morse code reception skill by novices: part-whole training.Deborah M. Clawson, Alice F. Healy, K. Anders Ericsson & Lyle E. Bourne - 2001 - Journal of Experimental Psychology: Applied 7 (2):129.
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  • Complex declarative learning.Michelene Th Chi & Stellan Ohlsson - 2005 - In K. Holyoak & B. Morrison (eds.), The Cambridge handbook of thinking and reasoning. Cambridge, England: Cambridge University Press.
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  • A psychobiological theory of attachment.Gary W. Kraemer - 1992 - Behavioral and Brain Sciences 15 (3):493-511.
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  • Emotions of human infants and mothers and development of the brain.Colwyn Trevarthen - 1992 - Behavioral and Brain Sciences 15 (3):524-525.
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  • P300 as the resolution of negative cortical DC shifts.L. Deecke & W. Lang - 1988 - Behavioral and Brain Sciences 11 (3):379.
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  • Useful ideas for exploiting time to engineer representations.Richard Rohwer - 1993 - Behavioral and Brain Sciences 16 (3):471-471.
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  • Dynamic-binding theory is not plausible without chaotic oscillation.Ichiro Tsuda - 1993 - Behavioral and Brain Sciences 16 (3):475-476.
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  • Must we solve the binding problem in neural hardware?James W. Garson - 1993 - Behavioral and Brain Sciences 16 (3):459-460.
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  • Rule acquisition and variable binding: Two sides of the same coin.P. J. Hampson - 1993 - Behavioral and Brain Sciences 16 (3):462-462.
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  • On the artificial intelligence paradox.Steffen Hölldobler - 1993 - Behavioral and Brain Sciences 16 (3):463-464.
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  • Distributing structure over time.John E. Hummel & Keith J. Holyoak - 1993 - Behavioral and Brain Sciences 16 (3):464-464.
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  • Time phases, pointers, rules and embedding.John A. Barnden - 1993 - Behavioral and Brain Sciences 16 (3):451-452.
    This paper is a commentary on the target article by Lokendra Shastri & Venkat Ajjanagadde [S&A]: “From simple associations to systematic reasoning: A connectionist representation of rules, variables and dynamic bindings using temporal synchrony” in same issue of the journal, pp.417–451. -/- It puts S&A's temporal-synchrony binding method in a broader context, comments on notions of pointing and other ways of associating information - in both computers and connectionist systems - and mentions types of reasoning that are a challenge to (...)
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  • Reasoning, learning and neuropsychological plausibility.Joachim Diederich - 1993 - Behavioral and Brain Sciences 16 (3):455-456.
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  • Locus-pocus.Carlo Semenza - 1994 - Behavioral and Brain Sciences 17 (1):80-80.
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  • Modularity need not imply locality: Damaged modules can have nonlocal effects.Edgar Zurif & David Swinney - 1994 - Behavioral and Brain Sciences 17 (1):89-90.
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  • Modularity, interaction and connectionist neuropsychology.Nick Chater - 1994 - Behavioral and Brain Sciences 17 (1):66-67.
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  • Further advantages of abandoning the locality assumption in face recognition.Jules Davidoff & Bernard Renault - 1994 - Behavioral and Brain Sciences 17 (1):68-68.
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  • Genes, specificity, and the lexical/functional distinction in language acquisition.Karin Stromswold - 1996 - Behavioral and Brain Sciences 19 (4):648-649.
    Contrary to Müller's claims, and in support of modular theories, genetic factors play a substantial and significant role in language. The finding that some children with specific language impairment (SLI) have nonlinguistic impairments may reflect improper diagnosis of SLI or impairments that are secondary to linguistic impairments. Thus, such findings do not argue against the modularity thesis. The lexical/functional distinction appears to be innate and specifically linguistic and could be instantiated in either symbolic or connectionist systems.
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  • Autonomy of syntactic processing and the role of Broca's area.Angela D. Friederici - 1996 - Behavioral and Brain Sciences 19 (4):634-635.
    Both autonomy and local specificity are compatible with observed interconnectivity at the cell level when considering two different levels: cell assemblies and brain systems. Early syntactic structuring processes in particular are likely to representan autonomous module in the language/brain system.
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  • (1 other version)A unified framework for addiction: Vulnerabilities in the decision process.Adam Johnson A. David Redish, Steve Jensen - 2008 - Behavioral and Brain Sciences 31 (4):415.
    The understanding of decision-making systems has come together in recent years to form a unified theory of decision-making in the mammalian brain as arising from multiple, interacting systems (a planning system, a habit system, and a situation-recognition system). This unified decision-making system has multiple potential access points through which it can be driven to make maladaptive choices, particularly choices that entail seeking of certain drugs or behaviors. We identify 10 key vulnerabilities in the system: (1) moving away from homeostasis, (2) (...)
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  • The sense of diachronic personal identity.Stan Klein - 2013 - Phenomenology and the Cognitive Sciences 12 (4):791-811.
    In this paper, I first consider a famous objection that the standard interpretation of the Lockean account of diachronicity (i.e., one’s sense of personal identity over time) via psychological connectedness falls prey to breaks in one’s personal narrative. I argue that recent case studies show that while this critique may hold with regard to some long-term autobiographical self-knowledge (e.g., episodic memory), it carries less warrant with respect to accounts based on trait-relevant, semantic self-knowledge. The second issue I address concerns the (...)
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  • Uncovering "Cultural Meaning": Problems and Solutions.Todd Jones - 2004 - Behavior and Philosophy 32 (2):247 - 268.
    In his highly influential "The Interpretation of Cultures," anthropologist Clifford Geertz argues that the study of culture ought to be "not an experimental science in search of law but an interpretive one in search of meaning." I argue that the two need not be opposed. The best way of making sense of the social scientific practice of looking at meaning is to see interpretivists as looking at typical mental reactions that people in a given culture have to certain acts and (...)
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  • The cry for the other: The biocultural womb of human development.James B. Ashbrook - 1994 - Zygon 29 (3):297-314.
    The human experience of meaning‐making lies at the roots of consciousness, creativity, and religious faith. It arises from the basic experience of separation from a loved object, suffered by all mammals, and, in general terms, from the experienced gap between ourselves and our environment. We fill the gap with transitional objects and symbols that reassure us of basic continuity in ourselves and in the world. These objects and symbols also serve the neurognostic function of demonstrating what the world is like. (...)
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  • The epistemology of evidence in cognitive neuroscience.William P. Bechtel - forthcoming - In Robert A. Skipper, Collin Allen, Rachel Ankeny, Carl F. Craver, Lindley Darden, Gregory Mikkelson & Robert C. Richardson (eds.), Philosophy and the Life Sciences: A Reader. MIT Press.
    It is no secret that scientists argue. They argue about theories. But even more, they argue about the evidence for theories. Is the evidence itself trustworthy? This is a bit surprising from the perspective of traditional empiricist accounts of scientific methodology according to which the evidence for scientific theories stems from observation, especially observation with the naked eye. These accounts portray the testing of scientific theories as a matter of comparing the predictions of the theory with the data generated by (...)
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  • The brain's 'new' science: Psychology, neurophysiology, and constraint.Gary Hatfield - 2000 - Philosophy of Science 67 (3):388-404.
    There is a strong philosophical intuition that direct study of the brain can and will constrain the development of psychological theory. When this intuition is tested against case studies on the neurophysiology and psychology of perception and memory, it turns out that psychology has led the way toward knowledge of neurophysiology. An abstract argument is developed to show that psychology can and must lead the way in neuroscientific study of mental function. The opposing intuition is based on mainly weak arguments (...)
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  • Psychoneural reduction of the genuinely cognitive: Some accomplished facts.John Bickle - 1995 - Philosophical Psychology 8 (3):265-85.
    The need for representations and computations over their contents in psychological explanations is often cited as both the mark of the genuinely cognitive and a source of skepticism about the reducibility of cognitive theories to neuroscience. A generic version of this anti-reductionist argument is rejected in this paper as unsound, since (i) current thinking about associative learning emphasizes the need for cognitivist resources in theories adequate to explain even the simplest form of this phenomena (Pavlovian conditioning), and yet (ii) the (...)
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  • Reconciling reinforcement learning models with behavioral extinction and renewal: Implications for addiction, relapse, and problem gambling.A. David Redish, Steve Jensen, Adam Johnson & Zeb Kurth-Nelson - 2007 - Psychological Review 114 (3):784-805.
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  • Conjunctive representations in learning and memory: Principles of cortical and hippocampal function.Randall C. O'Reilly & Jerry W. Rudy - 2001 - Psychological Review 108 (2):311-345.
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  • Modeling hippocampal and neocortical contributions to recognition memory: A complementary-learning-systems approach.Kenneth A. Norman & Randall C. O'Reilly - 2003 - Psychological Review 110 (4):611-646.
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  • Homing in on consciousness in the nervous system: An action-based synthesis.Ezequiel Morsella, Christine A. Godwin, Tiffany K. Jantz, Stephen C. Krieger & Adam Gazzaley - 2016 - Behavioral and Brain Sciences 39:1-70.
    What is the primary function of consciousness in the nervous system? The answer to this question remains enigmatic, not so much because of a lack of relevant data, but because of the lack of a conceptual framework with which to interpret the data. To this end, we have developed Passive Frame Theory, an internally coherent framework that, from an action-based perspective, synthesizes empirically supported hypotheses from diverse fields of investigation. The theory proposes that the primary function of consciousness is well-circumscribed, (...)
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  • Introduction to “Implicit memory: Multiple perspectives”.Daniel L. Schacter - 1990 - Bulletin of the Psychonomic Society 28 (4):338-340.
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  • Implicit memory, the serial position effect, and test awareness.John M. Rybash & Joyce L. Osborne - 1991 - Bulletin of the Psychonomic Society 29 (4):327-330.
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  • From epistemology to P3-ology.Rolf Verleger - 1988 - Behavioral and Brain Sciences 11 (3):399.
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  • Probability mismatch and template mismatch: A paradox in P300 amplitude?Albert Kok - 1988 - Behavioral and Brain Sciences 11 (3):388.
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  • Updating the context of ERP research.Merlin W. Donald - 1988 - Behavioral and Brain Sciences 11 (3):381.
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  • P300 and the validity of psychophysiological descriptions of behavior.Igor O. Aleksandrov & Natalia E. Maksimova - 1988 - Behavioral and Brain Sciences 11 (3):374.
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  • Is the P300 component a manifestation of context updating?Emanuel Donchin & Michael G. H. Coles - 1988 - Behavioral and Brain Sciences 11 (3):357.
    To understand the endogenous components of the event-related brain potential (ERP), we must use data about the components' antecedent conditions to form hypotheses about the information-processing function of the underlying brain activity. These hypotheses, in turn, generate testable predictions about the consequences of the component. We review the application of this approach to the analysis of the P300 component. The amplitude of the P300 is controlled multiplicatively by the subjective probability and the task relevance of the eliciting events, whereas its (...)
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  • Computational and biological constraints in the psychology of reasoning.Mike Oaksford & Mike Malloch - 1993 - Behavioral and Brain Sciences 16 (3):468-469.
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  • Toward a unified behavioral and brain science.Jerome A. Feldman - 1993 - Behavioral and Brain Sciences 16 (3):458-458.
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  • Could static binding suffice?Paul R. Cooper - 1993 - Behavioral and Brain Sciences 16 (3):453-454.
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  • No threat to modularity.Yosef Grodzinsky & Uri Hadar - 1994 - Behavioral and Brain Sciences 17 (1):70-71.
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  • Innateness, autonomy, universality, and the neurobiology of regular and irregular inflectional morphology.David Kemmerer - 1996 - Behavioral and Brain Sciences 19 (4):639-641.
    Müller's goal of bringing neuroscience to bear on controversies in linguistics is laudable. However, some of his specific proposals about innateness and autonomy are misguided. Recent studies on the neurobiology of regular and irregular inflectional morphology indicate that these two linguistic processes are subserved by anatomically and physiologically distinct neural subsystems, whose functional organization is likely to be under direct genetic control rather than assembled by strictly epigenetic factors.
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  • Double dissociation, modularity, and distributed organization.John A. Bullinaria & Nick Chater - 1996 - Behavioral and Brain Sciences 19 (4):632-632.
    Müller argues that double dissociations do not imply underlying modularity of the cognitive system, citing neural networks as examples of fully distributed systems that can give rise to double dissociations. We challenge this claim, noting that suchdouble dissociations typically do not “scale-up,” and that even some singledissociations can be difficult to account for in a distributed system.
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  • How to grow a human.Michael C. Corballis - 1996 - Behavioral and Brain Sciences 19 (4):632-633.
    I enlarge on the theme that the brain mechanisms required for languageand other aspects of the human mind evolved through selective changes in the regulatory genes governing growth. Extension of the period of postnatal growth increases the role of the environment in structuring the brain, and spatiotemporal programming (heterochrony) ofgrowth might explain hierarchical representation, hemispheric specialization, and perhaps sex differences.
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  • Russell on Mnemic Causation.Sven Bernecker - 2001 - Principia: An International Journal of Epistemology 5 (1-2):149-186.
    According to the standard view, the causal process connecting a past representation and its subsequent recall involves intermediary memory traces. Yet Bertrand Russell and Ludwig Wittgenstein held that since the physiological evidence for memory traces isn't quite conclusive, it is prudent to come up with an account of memory causation-referred to as nmemic causation—that manages without the stipulation of memory traces. Given mnemic causation, a past representation is directly causally active over a temporal distance. I argue that the stipulation of (...)
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  • Evolutionary conceptions of adaptation and brain design.Jay Schulkin - 1989 - World Futures 27 (1):1-15.
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  • Empathy and Imagination.Nancy Sherman - 1998 - Midwest Studies in Philosophy 22 (1):82-119.
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  • (1 other version)A unified framework for addiction: Vulnerabilities in the decision process.A. David Redish, Steve Jensen & Adam Johnson - 2008 - Behavioral and Brain Sciences 31 (4):415-437.
    The understanding of decision-making systems has come together in recent years to form a unified theory of decision-making in the mammalian brain as arising from multiple, interacting systems (a planning system, a habit system, and a situation-recognition system). This unified decision-making system has multiple potential access points through which it can be driven to make maladaptive choices, particularly choices that entail seeking of certain drugs or behaviors. We identify 10 key vulnerabilities in the system: (1) moving away from homeostasis, (2) (...)
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