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Conditioned Reflexes

Humana Mente 3 (11):380-383 (1928)

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  1. Moral Agency.Timothy Nailer - 2022 - Dissertation, University of Adelaide
    While there is a vast philosophical literature exploring the conditions under which it is appropriate to hold individuals morally responsible for their actions, relatively little attention has been paid to the related question of which kinds of individuals merit these responsibility ascriptions. Under normal circumstances, typical adult human beings are held morally responsible for their behaviour but infants and nonhuman animals are not. In this thesis, I aim to account for this difference. That is, I aim to give an analysis (...)
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  • Avian Emotions: Comparative Perspectives on Fear and Frustration.Mauricio R. Papini, Julio C. Penagos-Corzo & Andrés M. Pérez-Acosta - 2019 - Frontiers in Psychology 9:433390.
    Emotions are complex reactions that allow individuals to cope with significant positive and negative events. Research on emotion was pioneered by Darwin’s (1871) work on emotional expressions in humans and animals. But Darwin was concerned mainly with facial and bodily expressions of significance for humans, citing mainly examples from mammals (e.g., apes, dogs, and cats). In birds, emotional expressions are less evident for a human observer, so a different approach is needed. Understanding avian emotions will provide key evolutionary information on (...)
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  • Accuracy-based measures provide a better measure of sequence learning than reaction time-based measures.Kristi Urry, Nicholas R. Burns & Irina Baetu - 2015 - Frontiers in Psychology 6:153321.
    The Serial Reaction Time Task (SRTT) was designed to measure motor sequence learning and is widely used in many fields in cognitive science and neuroscience. However, the common performance measures derived from SRTT—reaction time (RT) difference scores—may not provide valid measures of sequence learning. This is because RT-difference scores may be subject to floor effects and otherwise not sufficiently reflective of learning. A ratio RT measure might minimize floor effects. Furthermore, measures derived from predictive accuracy may provide a better assessment (...)
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  • The hippocampus as episodic encoder: Does it play tag?Robert H. I. Dale - 1985 - Behavioral and Brain Sciences 8 (3):499-500.
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  • Effects of hippocampal lesions on some operant visual discrimination tasks.Michael L. Woodruff & Dennis L. Whittington - 1985 - Behavioral and Brain Sciences 8 (3):513-514.
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  • The Emotional Dog and Its Rational Tail: A Social Intuitionist Approach to Moral Judgment.Jonathan Haidt - 2001 - Psychological Review 108 (4):814-834.
    Research on moral judgment has been dominated by rationalist models, in which moral judgment is thought to be caused by moral reasoning. The author gives 4 reasons for considering the hypothesis that moral reasoning does not cause moral judgment; rather, moral reasoning is usually a post hoc construction, generated after a judgment has been reached. The social intuitionist model is presented as an alternative to rationalist models. The model is a social model in that it deemphasizes the private reasoning done (...)
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  • The physiology of Descartes and its modern developments.J. S. Haldane - 1935 - Acta Biotheoretica 1 (1-2):5-16.
    Nach einer kurzen Übersicht überDescartes' mechanistiche Theorie der somatischen Funktionen und der Reproduktion, wird in der vorliegenden Arbeit die Entwicklung dieser Theorie bis zur neuesten Zeit beschrieben. Sodann wird eine Übersicht gegeben über die vitalistische Theorie, welche unter wissenschaftlichen Forschern bis zur Mitte des vorigen Jahrhunderts vorherrschte. Dann werden die Gründe dafür angegeben, dass diese Theorie des Vitalismus ungefähr um diese Zeit verlassen wurde, um durch die mechanistische Theorie ersetzt zu werden. Diese ihrerseits ist jedoch auf einer unbegründeten metaphysischen Auffassung (...)
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  • The function of phenomenal states: Supramodular interaction theory.Ezequiel Morsella - 2005 - Psychological Review 112 (4):1000-1021.
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  • Memory buffer and comparator can share the same circuitry.J. A. Gray - 1985 - Behavioral and Brain Sciences 8 (3):501-501.
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  • A Bio-Logical Theory of Animal Learning.David Guez - 2009 - Biological Theory 4 (2):148-158.
    This article provides the foundation for a new predictive theory of animal learning that is based upon a simple logical model. The knowledge of experimental subjects at a given time is described using logical equations. These logical equations are then used to predict a subject’s response when presented with a known or a previously unknown situation. This new theory suc- cessfully anticipates phenomena that existing theories predict, as well as phenomena that they cannot. It provides a theoretical account for phenomena (...)
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  • Contagious itch: what we know and what we would like to know.C. Schut, S. Grossman, U. Gieler, J. Kupfer & G. Yosipovitch - 2015 - Frontiers in Human Neuroscience 9:119849.
    All humans experience itch in the course of their life. Even a discussion on the topic of itch or seeing people scratch can evoke the desire to scratch. These events are coined ‘contagious itch’ and are very common. We and others have shown that videos showing people scratching and pictures of affected skin or insects can induce itch in healthy persons and chronic itch patients. In our studies, patients with atopic dermatitis were more susceptible to visual itch cues than healthy. (...)
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  • Fears, phobias and preparedness: Toward an evolved module of fear and fear learning.Arne Öhman & Susan Mineka - 2001 - Psychological Review 108 (3):483-522.
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  • Aversive Learning and Trait Aggression Influence Retaliatory Behavior.Tanaz Molapour, Björn Lindström & Andreas Olsson - 2016 - Frontiers in Psychology 7.
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  • On the hippocampus, time, and interference.Leonard E. Jarrard - 1985 - Behavioral and Brain Sciences 8 (3):503-504.
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  • The hippocampus, synaptic enhancement, and intermediate-term memory.B. L. McNaughton & C. A. Barnes - 1985 - Behavioral and Brain Sciences 8 (3):507-508.
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  • The Two Skinners, Modern and Postmodern.Roy A. Moxley - 1999 - Behavior and Philosophy 27 (2):97 - 125.
    Different accounts of Skinner's work are often in conflict. Some interpretations, for example, regard Skinner as a mechanist. Other interpretations regard Skinner as a selectionist. An alternative interpretation is to see Skinner as employing both views with changes in these views and their proportionate relations over time. To clarify these distinctions, it is helpful to see Skinner's work against the background of similar changes that have been taking place in Western Culture. An extended and overlapping shift in cultural values has (...)
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  • The uses of trauma in experiment: Traumatic stress and the history of experimental neurosis, c. 1925–1975.Ulrich Koch - 2019 - Science in Context 32 (3):327-351.
    ArgumentThe article retraces the shifting conceptualizations of psychological trauma in experimental psychopathological research in the middle decades of the twentieth century in the United States. Among researchers studying so-called experimental neuroses in animal laboratories, trauma was an often-invoked category used to denote the clash of conflicting forces believed to lead to neurotic suffering. Experimental psychologists, however, soon grew skeptical of the traumatogenic model and ultimately came to reject neurosis as a disease entity. Both theoretical differences and practical circumstances, such as (...)
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  • A Common Framework for Theories of Norm Compliance.Adam Morris & Fiery Cushman - 2018 - Social Philosophy and Policy 35 (1):101-127.
    Abstract:Humans often comply with social norms, but the reasons why are disputed. Here, we unify a variety of influential explanations in a common decision framework, and identify the precise cognitive variables that norms might alter to induce compliance. Specifically, we situate current theories of norm compliance within the reinforcement learning framework, which is widely used to study value-guided learning and decision-making. This framework offers an appealingly precise language to distinguish between theories, highlights the various points of convergence and divergence, and (...)
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  • A modern learning theory perspective on the etiology of panic disorder.Mark E. Bouton, Susan Mineka & David H. Barlow - 2001 - Psychological Review 108 (1):4-32.
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  • The role of stress in social decision-making.Bo Ra Lee - unknown
    Although a substantial literature is developing regarding the effects of stress on decision-making, the literature on stress and social decision-making is still in the beginning stage. The present research extends this new literature by examining the mediating and moderating factors of the effect of stress on social decision-making. Furthermore, a novel aspect of the research is its effort to connect the information-processing and functional perspectives, with regard to the acute stress response. Dual-mode theories state that emotional processing, relative to cognitive (...)
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  • The development of theory: Logic of method or underlying processes?Charles P. Shimp - 1985 - Behavioral and Brain Sciences 8 (3):511-512.
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  • Associations across time: The hippocampus as a temporary memory store.J. N. P. Rawlins - 1985 - Behavioral and Brain Sciences 8 (3):479-497.
    All recent memory theories of hippocampal function have incorporated the idea that the hippocampus is required to process items only of some qualitatively specifiahle kind, and is not required to process items of some complementary set. In contrast, it is now proposed that the hippocampus is needed to process stimuli of all kinds, but only when there is a need to associate those stimuli with other events that are temporally discontiguous. In order to form or use temporally discontiguous associations, it (...)
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  • Animal concepts: Content and discontent.Nick Chater & Cecilia Heyes - 1994 - Mind and Language 9 (3):209-246.
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  • Persuasion with Limited Sight.Alex Lascarides & Markus Guhe - 2019 - Review of Philosophy and Psychology 10 (1):1-33.
    Humans face many game problems that are too large for the whole game tree to be used in their deliberations about action, and very little is understood about how they cope in such scenarios. However, when a human player’s chosen strategy is conditioned on her limited perspective of how the game might progress, then it should be possible to manipulate her into changing her planned move by mentioning a possible outcome of an alternative move. This paper demonstrates that human players (...)
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  • Cellular perception and misperception: Internal models for decision‐making shaped by evolutionary experience.Amir Mitchell & Wendell Lim - 2016 - Bioessays 38 (9):845-849.
    Cells live in dynamic environments that necessitate perpetual adaptation. Since cells have limited resources to monitor external inputs, they are required to maximize the information content of perceived signals. This challenge is not unique to microscopic life: Animals use senses to perceive inputs and adequately respond. Research showed that sensory‐perception is actively shaped by learning and expectation allowing internal cognitive models to “fill in the blanks” in face of limited information. We propose that cells employ analogous strategies and use internal (...)
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  • Three-store theories of memory.William S. Maki - 1985 - Behavioral and Brain Sciences 8 (3):505-506.
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  • Empiricist versus prototype theories of language acquisition.Nathan Stemmer - 1989 - Mind and Language 4 (3):201-221.
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  • Sharpening the focus on functions of the hippocampus.Daniel P. Kimble - 1985 - Behavioral and Brain Sciences 8 (3):504-505.
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  • A Computational Analysis of Aberrant Delay Discounting in Psychiatric Disorders.Giles W. Story, Michael Moutoussis & Raymond J. Dolan - 2015 - Frontiers in Psychology 6.
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  • Temporal discontiguity: Alternative to, or component of, existing theories of hippocampal function?Donna J. Hughey - 1985 - Behavioral and Brain Sciences 8 (3):501-502.
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  • Forgetting the Past and Neglecting the Future. Commentary: A Crisis in Comparative Psychology: Where Have All the Undergraduates Gone?Marco Vasconcelos & Josefa N. S. Pandeirada - 2015 - Frontiers in Psychology 6.
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  • Tourette-like behaviors in the normal population are associated with hyperactive/impulsive ADHD-like behaviors but do not relate to deficits in conditioned inhibition or response inhibition.Nadja Heym, Ebrahim Kantini, Hannah L. R. Checkley & Helen J. Cassaday - 2014 - Frontiers in Psychology 5:99196.
    Attention-Deficit Hyperactivity Disorder (ADHD) and Tourette Syndrome (TS) present as distinct conditions clinically; however, comorbidity and inhibitory control deficits have been proposed for both. Whilst such deficits have been studied widely within clinical populations, findings are mixed—partly due to comorbidity and/or medication effects—and studies have rarely distinguished between subtypes of the disorders. Studies in the general population are sparse. Using a continuity approach, the present study examined (i) the relationships between inattentive and hyperactive/impulsive aspects of ADHD and TS-like behaviors in (...)
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  • The Orienting Response in Healthy Aging: Novelty P3 Indicates No General Decline but Reduced Efficacy for Fast Stimulation Rates.Stefan Berti, Gerhard Vossel & Matthias Gamer - 2017 - Frontiers in Psychology 8.
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  • Minding the general memory store: Further consideration of the role of the hippocampus in memory.Neal J. Cohen & Matthew Shapiro - 1985 - Behavioral and Brain Sciences 8 (3):498-499.
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  • The hippocampus and time.Gordon Winocur - 1985 - Behavioral and Brain Sciences 8 (3):512-513.
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  • Gaming the gamer? – The ethics of exploiting psychological research in video games.Johnny Hartz Søraker - 2016 - Journal of Information, Communication and Ethics in Society 14 (2):106-123.
    The purpose of this paper is to investigate the ethical implications of video game companies employing psychologists and using psychological research in game design.,The author first argues that exploiting psychology in video games may be more ethically problematic than familiar application domains like advertising, gambling and political rhetoric. Then an overview of the effects particular types of game design may have on user behavior is provided, taking into account various findings and phenomena from behavioral psychology and behavioral economics.,Finally, the author (...)
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  • Memory processing by the brain: Subregionalization, species-dependency, and network character.Hans J. Markowitsch - 1985 - Behavioral and Brain Sciences 8 (3):506-507.
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  • Time and hippocampal lesion effects: Tempus edax rerum?J. N. P. Rawlins - 1985 - Behavioral and Brain Sciences 8 (3):514-528.
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  • Discontiguity and memory.David S. Olton - 1985 - Behavioral and Brain Sciences 8 (3):510-511.
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  • The Contribution of the Amygdala to Aversive and Appetitive Pavlovian Processes.Justin M. Moscarello & Joseph E. LeDoux - 2013 - Emotion Review 5 (3):248-253.
    Pavlovian cues predict the occurrence of motivationally salient outcomes, thus serving as an important trigger of approach and avoidance behavior. The amygdala is a key substrate of Pavlovian conditioning, and the nature of its contribution varies by the motivational valence of unconditioned stimuli. The literature on aversive Pavlovian learning supports a serial-processing model of amygdalar function, while appetitive studies suggest that Pavlovian associations are processed through parallel circuits in the amygdala. It is proposed that serial and parallel forms of information (...)
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  • Hippocampus and “general” mnemonic function: Only time will tell.Warren H. Meck - 1985 - Behavioral and Brain Sciences 8 (3):509-510.
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  • Is the hippocampus a store, intermediate or otherwise?Neil McNaughton - 1985 - Behavioral and Brain Sciences 8 (3):508-509.
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  • Appetitive and Defensive Motivation: Goal-Directed or Goal-Determined?Peter J. Lang & Margaret M. Bradley - 2013 - Emotion Review 5 (3):230-234.
    Our view is that fundamental appetitive and defensive motivation systems evolved to mediate a complex array of adaptive behaviors that support the organism’s drive to survive—defending against threat and securing resources. Activation of these motive systems engages processes that facilitate attention allocation, information intake, sympathetic arousal, and, depending on context, will prompt tactical actions that can be directed either toward or away from the strategic goal, whether defensively or appetitively determined. Research from our laboratory that measures autonomic, central, and somatic (...)
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  • Does our behavioral methodology conceal the deficit caused by hippocampal damage?David T. D. James - 1985 - Behavioral and Brain Sciences 8 (3):502-503.
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  • Neural Dynamics of Autistic Repetitive Behaviors and Fragile X Syndrome: Basal Ganglia Movement Gating and mGluR-Modulated Adaptively Timed Learning.Stephen Grossberg & Devika Kishnan - 2018 - Frontiers in Psychology 9.
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  • Interference Conditions of the Reconsolidation Process in Humans: The Role of Valence and Different Memory Systems.Rodrigo S. Fernández, Luz Bavassi, Laura Kaczer, Cecilia Forcato & María E. Pedreira - 2016 - Frontiers in Human Neuroscience 10.
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  • A physiological basis for hippocampal involvement in coding temporally discontiguous events.Sam A. Deadwyler - 1985 - Behavioral and Brain Sciences 8 (3):500-501.
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  • Toward an Understanding of Dynamic Moral Decision Making: Model-Free and Model-Based Learning.George I. Christopoulos, Xiao-Xiao Liu & Ying-yi Hong - 2017 - Journal of Business Ethics 144 (4):699-715.
    In business settings, decision makers facing moral issues often experience the challenges of continuous changes. This dynamic process has been less examined in previous literature on moral decision making. We borrow theories on learning strategies and computational models from decision neuroscience to explain the updating and learning mechanisms underlying moral decision processes. Specifically, we present two main learning strategies: model-free learning, wherein the values of choices are updated in a trial-and-error fashion sustaining the formation of habits and model-based learning, wherein (...)
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  • Another hippocampal theory.Marc N. Branch - 1985 - Behavioral and Brain Sciences 8 (3):497-498.
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