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What is it like to be a bat?

In Mortal questions. New York: Cambridge University Press. pp. 435 - 450 (1979)

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  1. Communication versus discrimination.Valerie Gray Hardcastle - 1993 - Behavioral and Brain Sciences 16 (4):649-650.
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  • No report; no feeling.Lawrence H. Davis - 1993 - Behavioral and Brain Sciences 16 (4):647-648.
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  • Animal communication of private states does not illuminate the human case.Selmer Bringsjord & Elizabeth Bringsjord - 1993 - Behavioral and Brain Sciences 16 (4):645-646.
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  • The status of private events in behavior analysis.William M. Baum - 1993 - Behavioral and Brain Sciences 16 (4):644-644.
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  • Perhaps Sisyphus is the relevant model for animal-language researchers.Donald M. Baer - 1993 - Behavioral and Brain Sciences 16 (4):642-643.
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  • Toad's prey-catching: A complex system with heuristic value.Jörg-Peter Ewert - 1987 - Behavioral and Brain Sciences 10 (3):389-405.
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  • Implicit versus explicit computation.Kent A. Stevens - 1987 - Behavioral and Brain Sciences 10 (3):387-388.
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  • Intelligent neurons.G. Székely - 1987 - Behavioral and Brain Sciences 10 (3):388-389.
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  • Neuroethology and color vision in amphibians.S. L. Kondrashev - 1987 - Behavioral and Brain Sciences 10 (3):385-385.
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  • Worm detector replaced by network model – but still a bit worm-infested.Gerhard Roth & Kiisa Nishikawa - 1987 - Behavioral and Brain Sciences 10 (3):385-386.
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  • Sensorimotor maps in the tectum.A. Roucoux & M. Crommelinck - 1987 - Behavioral and Brain Sciences 10 (3):386-387.
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  • Sampling and information processing.Edward Gruberg - 1987 - Behavioral and Brain Sciences 10 (3):381-382.
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  • Presumptions based on keyhole peeping.G. A. Horridge - 1987 - Behavioral and Brain Sciences 10 (3):382-383.
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  • Ewert's model: Some discoveries and some difficulties.David Ingle - 1987 - Behavioral and Brain Sciences 10 (3):383-385.
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  • The compleat visual system: From input to output.M. A. Goodale - 1987 - Behavioral and Brain Sciences 10 (3):379-380.
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  • The nervous system/behavior interface: Levels of organization and levels of approach.Paul Grobstein - 1987 - Behavioral and Brain Sciences 10 (3):380-381.
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  • Ethological invariants: Boxes, rubber bands, and biological processes.John C. Fentress - 1987 - Behavioral and Brain Sciences 10 (3):377-378.
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  • Prey-catching in toads: An exceptional neuroethological model.Seven O. E. Ebbesson - 1987 - Behavioral and Brain Sciences 10 (3):375-376.
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  • Networks with evolutionary potential.Günter Ehret - 1987 - Behavioral and Brain Sciences 10 (3):376-377.
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  • Toward a reformulation of the command concept.Randolf DiDomenico & Robert C. Eaton - 1987 - Behavioral and Brain Sciences 10 (3):374-375.
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  • Has the greedy toad lost its soul; and if so, what was it?Robert W. Doty - 1987 - Behavioral and Brain Sciences 10 (3):375-375.
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  • Sensorimotor functions: What is a command, that a code may yield it?Christopher M. Comer - 1987 - Behavioral and Brain Sciences 10 (3):372-372.
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  • Advantages of experimentation in neuroscience.Michael A. Arbib - 1987 - Behavioral and Brain Sciences 10 (3):368-369.
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  • Ethology and physiology: A happy marriage.Gerard P. Baerends - 1987 - Behavioral and Brain Sciences 10 (3):369-370.
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  • After the sensory analysers: Problems with concepts and terminology.D. M. Broom - 1987 - Behavioral and Brain Sciences 10 (3):370-371.
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  • How is a toad not like a bug?Jeffrey M. Camhi - 1987 - Behavioral and Brain Sciences 10 (3):371-372.
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  • Neuroethology of releasing mechanisms: Prey-catching in toads.Jörg-Peter Ewert - 1987 - Behavioral and Brain Sciences 10 (3):337-368.
    Abstract“Sign stimuli” elicit specific patterns of behavior when an organism's motivation is appropriate. In the toad, visually released prey-catching involves orienting toward the prey, approaching, fixating, and snapping. For these action patterns to be selected and released, the prey must be recognized and localized in space. Toads discriminate prey from nonprey by certain spatiotemporal stimulus features. The stimulus-response relations are mediated by innate releasing mechanisms (RMs) with recognition properties partly modifiable by experience. Striato-pretecto-tectal connectivity determines the RM's recognition and localization (...)
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  • More on prosopagnosia.Andrew W. Young - 1995 - Behavioral and Brain Sciences 18 (2):271-271.
    Some cases of prosopagnosia involve a highly circumscribed loss of A-consciousness. When seen in this way they offer further support for the arguments made in Block's target article.
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  • Feeling of knowing and phenomenal consciousness.Tiziana Zalla & Adriano P. Palma - 1995 - Behavioral and Brain Sciences 18 (2):271-272.
    In Feeling of Knowing cases, subjects have a form of consciousness about the presence of a content (such as an item of information) without having access to it. If this phenomenon can be correctly interpreted as having to do with consciousness, then there would be a P-conscious mental experience which is dissociated from access.
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  • Consciousness is not a natural kind.J. van Brakel - 1995 - Behavioral and Brain Sciences 18 (2):269-270.
    Blocks distinction between “phenomenal feel” consciousness and “thought/cognition” consciousness is a cultural construction. Consciousness (and its “subspecies”) is not a natural kind. Some crosscultural data are presented to support this.
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  • Access denied.Dan Lloyd - 1995 - Behavioral and Brain Sciences 18 (2):261-262.
    The information processing that constitutes accessconsciousness is not sufficient to make a representational state conscious in any sense. Standard examples of computation without consciousness undermine A-consciousness, and Block's cases seem to derive their plausibility from a lurking phenomenal awareness. That is, people and other minded systems seem to have access-consciousness only insofar as the state accessed is a phenomenal one, or the state resulting from access is phenomenal, or both.
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  • Breakthrough on the consciousness front or much ado about nothing?N. F. Dixon - 1995 - Behavioral and Brain Sciences 18 (2):253-254.
    Propositions as to the nature of consciousness, based on disorders of perception that result from brain damage, and taking insufficient account of the numerous ways in which normal subjects may deviate from that “usual” sequence of events (input → subjective awareness → output) risk increasing rather than diminishing any existing confusion about the function of consciousness.
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  • Are blind babies delayed in achieving social understanding?Carol Slater - 1996 - Behavioral and Brain Sciences 19 (1):141-142.
    Barresi & Moore's account predicts that infants deprived of visual input will be delayed in achieving social understanding, a hypothesis that receives some support from studies of language use. by blind children. It is proposed that recently developed false belief and appearance/reality tasks be used to explore this issue further. Three possibly distracting conceptual issues are also discussed.
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  • Four-year-old humans are different: Why?Katherine Nelson - 1996 - Behavioral and Brain Sciences 19 (1):134-135.
    The intentionality schema is an abstraction that relates phylogenetic and ontogenetic sequences of social understanding, but it also obscures the differences between humans and other primates. In particular, it ignores human social developmental and communicative history and the important roles that language plays in human understanding of others' intentional states.
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  • Understanding that looking causes knowing.David R. Olson & Bruce Homer - 1996 - Behavioral and Brain Sciences 19 (1):135-135.
    Barresi & Moore provide an impressive account of how the coordination of first and third person information about the self and other could produce an account of intentional relations. They are less explicit as to how the child comes to understand the basic epistemic relation between experience and knowledge, that is, how informational access causes belief. We suggest one route.
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  • Ontogeny, evolution, and folk psychology.Daniel J. Povinelli, Mia C. Zebouni & Christopher G. Prince - 1996 - Behavioral and Brain Sciences 19 (1):137-138.
    Barresi & Moore assume an equivalence between ontogenetic and evolutionaiy transformations of social understanding. The mechanisms of evolution allow for novel structures to arise, both through terminal addition and through the onset of novel pathways at time points that precede the end points of ancestral pathways. Terminal addition may not be the appropriate model for the evolution of human object-directed imitation, intermodal equivalence, or joint attention.
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  • Self-knowledge, knowledge of other minds, and kinesthetic-visual matching.Robert W. Mitchell - 1996 - Behavioral and Brain Sciences 19 (1):133-133.
    The “intentional schema” seems identical to or dependent upon kinesthetic–visual matching, both of which account for similar empirical findings. The intentional schema, however, fails to account for variability in children's understanding of false belief and differences in children's understanding of self and other in pretense.
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  • But what is the intentional schema?Adam Morton - 1996 - Behavioral and Brain Sciences 19 (1):133-134.
    The intentional schema may not be sufficiently characterized to make questions about its role in individual and species development intelligible. The idea of metarepresentation may perhaps give it enough content. The importance of metarepresentation itself, however, can be called into question.
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  • An ambiguity.Jennifer Church - 1996 - Behavioral and Brain Sciences 19 (1):126-127.
    The difference between first and third person information may be thought of as a difference in either informationalcontentor informationalmodality. Each option faces some problems. I try to sort out some of these issues and raise a question about the explanatory force of the notion of a schema.
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  • On the dangers of oversimulation.Gergely Csibra & György Gergely - 1996 - Behavioral and Brain Sciences 19 (1):127-128.
    Barresi & Moore fail to provide a satisfactory account for the development of social understanding because of (1) their ambiguous characterization of the relationship between the intentional schema and shared intentional activities, (2) their underestimation of the representational capacities of infants, and (3) their overreliance on the simulationist assumption that understanding others is tantamount to sharing their experience.
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  • First person representations need a methodology based on simulation or theory.Robert M. Gordon - 1996 - Behavioral and Brain Sciences 19 (1):130-131.
    Although their thesis is generally sound, Barresi & Moore give insufficient attention to the need for a methodology, whether simulation based or theory-based, for choosing among alternative possible matches of first person and third person information. This choice must be sensitive to contextual information, including past behavior. Moreover, apart from simulation or theory, first person information would not help predict future behavior.
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  • Imagination and imitation: Input, acid test, or alchemy?C. M. Heyes - 1996 - Behavioral and Brain Sciences 19 (1):131-132.
    Immediate imitation is likely to be a major, direct input to Barresi & Moore's level 2 competence, but deferred imitation is unlikely to play a key role in the transition to level 3, because (1) the attribution of first person knowledge is neither a necessary cause nor an obvious consequence of deferred imitation, and (2) deferred imitation does not correlate phylogenetically with capacities that more plausibly either yield or reflect a concept of intentional agency.
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  • Development of social emotions and constructive agents.Aaron Ben Ze'ev & Keith Oatley - 1996 - Behavioral and Brain Sciences 19 (1):124-125.
    The psychology of emotions illuminates the questions of intentional capacities raised by Barresi & Moore (B&M). Complex emotions require the development of a sense of self and are based on social comparisons between mainly imagined objects. The fourth level in B&M's framework requires something like a constructive agent rather than a mental agent.
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  • Die Eigenständigkeit des Krankheitsbegriffs in der Psychiatrie.Thomas Schramme - 2012 - Deutsche Zeitschrift für Philosophie 60 (6):955-970.
    Does the reference to a mental realm in using the notion of mental disorder lead to a dilemma that consists in either implying a Cartesian account of the mind-body relation or in the need to give up a notion of mental disorder in its own right? Many psychiatrists seem to believe that denying substance dualism requires a purely neurophysiological stance for explaining mental disorder. However, this conviction is based on a limited awareness of the philosophical debate on the mind-body problem. (...)
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  • Ants Are Not Conscious.Russell K. Standish - 2013 - Open Journal of Philosophy 3 (1):1-4.
    Anthropic reasoning is a form of statistical reasoning based upon finding oneself a member of a particular reference class of conscious beings. By considering empirical distribution functions defined over animal life on Earth, we can deduce that the vast bulk of animal life is unlikely to be conscious.
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  • Incorporating the Philosophy of Technology into Animal Welfare Assessment.Courtney Lynd Daigle - 2014 - Journal of Agricultural and Environmental Ethics 27 (4):633-647.
    Changes in attitudes towards how animals are housed in agriculture are currently under question in the public eye—particularly for laying hens. Many arguments from the rights and utilitarian viewpoints have been made for changing environmental conditions and managerial practices for animals in an effort to respect the interests of the animal and better their welfare. Yet, these arguments have been based upon belief systems that were developed from information that can be collected by human perception only. Technological advancements can facilitate (...)
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  • Theories of emotion causation: A review.Agnes Moors - 2009 - Cognition and Emotion 23 (4):625-662.
    I present an overview of emotion theories, organised around the question of emotion causation. I argue that theories of emotion causation should ideally address the problems of elicitation, intensity, and differentiation. Each of these problems can be divided into a subquestion that asks about the relation between stimuli and emotions (i.e., the functional level of process description, cf. Marr, 1982) and a subquestion that asks about the mechanism and representations that intervene (i.e., the algorithmic level of process description). The overview (...)
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  • Safe/Moral Autopoiesis and Consciousness.Mark R. Waser - 2013 - International Journal of Machine Consciousness 5 (1):59-74.
    Artificial intelligence, the "science and engineering of intelligent machines", still has yet to create even a simple "Advice Taker" [McCarthy, 1959]. We have previously argued [Waser, 2011] that this is because researchers are focused on problem-solving or the rigorous analysis of intelligence (or arguments about consciousness) rather than the creation of a "self" that can "learn" to be intelligent. Therefore, following expert advice on the nature of self [Llinas, 2001; Hofstadter, 2007; Damasio, 2010], we embarked upon an effort to design (...)
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  • The Irrationality of Physicalism.Pat Lewtas - 2014 - Axiomathes 24 (3):313-341.
    This paper argues, not that physicalism is wrong, but that it is irrational. The paper defines standards of rationality, both metaphysical and epistemological, that physicalism necessarily inherits from science. Then it assesses physicalist efforts to naturalize consciousness in light of these. It concludes that physicalism allows its metaphysics to outrun its epistemology, in defiance of applicable standards, revealing a fundamental incoherence in the doctrine. The paper also briefly reviews other naturalization programs, to claim that physicalism, unlike the sciences, hasn’t proved (...)
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