<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"><channel rdf:about="http://onlinelibrary.wiley.com/rss/journal/10.1111/(ISSN)1469-8986" xmlns="http://purl.org/rss/1.0/"><title>Psychophysiology</title><description> Wiley Online Library : Psychophysiology</description><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2F%28ISSN%291469-8986</link><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc</dc:publisher><dc:language xmlns:dc="http://purl.org/dc/elements/1.1/">en</dc:language><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/">© 2013 by the Society for Psychophysiological Research</dc:rights><prism:issn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">0048-5772</prism:issn><prism:eIssn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1469-8986</prism:eIssn><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-06-01T00:00:00-05:00</dc:date><prism:coverDisplayDate xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">June 2013</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">50</prism:volume><prism:number xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">6</prism:number><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">505</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">593</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1111/psyp.2013.50.issue-6/asset/cover.gif?v=1&amp;s=5300f9500342305910a11ce08177ef79da93990f"/><items><rdf:Seq><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12052"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12049"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12055"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12054"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12053"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12051"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12045"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12044"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12047"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12050"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12048"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12046"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1469-8986.2011.1208.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1469-8986.2011.1202.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12039"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12036"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12038"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12042"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12035"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12040"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12041"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12043"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12037"/></rdf:Seq></items></channel><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12052" xmlns="http://purl.org/rss/1.0/"><title>Decision making and action implementation: Evidence for an early visually triggered motor activation specific to potential actions</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12052</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Decision making and action implementation: Evidence for an early visually triggered motor activation specific to potential actions</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christophe Tandonnet, Michael I. Garry, Jeffery J. Summers</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-16T04:57:43.189394-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12052</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12052</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12052</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>To make a decision may rely on accumulating evidence in favor of one alternative until a threshold is reached. Sequential-sampling models differ by the way of accumulating evidence and the link with action implementation. Here, we tested a model's prediction of an early action implementation specific to potential actions. We assessed the dynamics of action implementation in go/no-go and between-hand choice tasks by transcranial magnetic stimulation of the motor cortex (single- or paired-pulse TMS; 3-ms interstimulus interval). Prior to implementation of the selected action, the amplitude of the motor evoked potential first increased whatever the visual stimulus but only for the hand potentially involved in the to-be-produced action. These findings suggest that visual stimuli can trigger an early motor activation specific to potential actions, consistent with race-like models with continuous transmission between decision making and action implementation.</p></div>
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To make a decision may rely on accumulating evidence in favor of one alternative until a threshold is reached. Sequential-sampling models differ by the way of accumulating evidence and the link with action implementation. Here, we tested a model's prediction of an early action implementation specific to potential actions. We assessed the dynamics of action implementation in go/no-go and between-hand choice tasks by transcranial magnetic stimulation of the motor cortex (single- or paired-pulse TMS; 3-ms interstimulus interval). Prior to implementation of the selected action, the amplitude of the motor evoked potential first increased whatever the visual stimulus but only for the hand potentially involved in the to-be-produced action. These findings suggest that visual stimuli can trigger an early motor activation specific to potential actions, consistent with race-like models with continuous transmission between decision making and action implementation.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12049" xmlns="http://purl.org/rss/1.0/"><title>Modulated neural processing of Western harmony in folk musicians</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12049</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Modulated neural processing of Western harmony in folk musicians</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Elvira Brattico, Tiina Tupala, Enrico Glerean, Mari Tervaniemi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-09T03:12:03.406967-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12049</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12049</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12049</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>A chord deviating from the conventions of Western tonal music elicits an early right anterior negativity (ERAN) in inferofrontal brain regions. Here, we tested whether the ERAN is modulated by expertise in more than one music culture, as typical of folk musicians. Finnish folk musicians and nonmusicians participated in electroencephalography recordings. The cadences consisted of seven chords. In incongruous cadences, the third, fifth, or seventh chord was a Neapolitan. The ERAN to the Neapolitans was enhanced in folk musicians compared to nonmusicians. Folk musicians showed an enhanced P3a for the ending Neapolitan. The Neapolitan at the fifth position was perceived differently and elicited a late enhanced ERAN in folk musicians. Hence, expertise in more than one music culture seems to modify chord processing by enhancing the ERAN to ambivalent chords and the P3a to incongruous chords, and by altering their perceptual attributes.</p></div>
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A chord deviating from the conventions of Western tonal music elicits an early right anterior negativity (ERAN) in inferofrontal brain regions. Here, we tested whether the ERAN is modulated by expertise in more than one music culture, as typical of folk musicians. Finnish folk musicians and nonmusicians participated in electroencephalography recordings. The cadences consisted of seven chords. In incongruous cadences, the third, fifth, or seventh chord was a Neapolitan. The ERAN to the Neapolitans was enhanced in folk musicians compared to nonmusicians. Folk musicians showed an enhanced P3a for the ending Neapolitan. The Neapolitan at the fifth position was perceived differently and elicited a late enhanced ERAN in folk musicians. Hence, expertise in more than one music culture seems to modify chord processing by enhancing the ERAN to ambivalent chords and the P3a to incongruous chords, and by altering their perceptual attributes.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12055" xmlns="http://purl.org/rss/1.0/"><title>Cardiovascular down-regulation in essential hypotension: Relationships with autonomic control and sleep</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12055</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cardiovascular down-regulation in essential hypotension: Relationships with autonomic control and sleep</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Naima Covassin, Massimiliano Zambotti, Nicola Cellini, Michela Sarlo, Luciano Stegagno</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-08T21:24:06.451484-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12055</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12055</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12055</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In this work, we aimed to clarify the autonomic involvement in the cardiovascular down-regulation in essential hypotension. The relationships between cardiovascular response and sleep quality were also examined. Thirteen female hypotensives and 13 female normotensives performed a stress task followed by polysomnography. Measures derived from blood pressure monitoring, impedance cardiography, and heart rate variability were collected. Hypotensives exhibited lower cardiovascular and autonomic activation than controls during the task. While a better sleep quality (i.e., higher sleep efficiency and lower nocturnal wakefulness) correlated with a reduced reactivity in normotensives, the opposite pattern occurred in hypotensives. The results suggest that a blunted response in both autonomic branches underlies the cardiovascular hypoactivation in hypotension. Further, good sleep seems to be associated with optimal levels of physiological reactivity.</p></div>
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In this work, we aimed to clarify the autonomic involvement in the cardiovascular down-regulation in essential hypotension. The relationships between cardiovascular response and sleep quality were also examined. Thirteen female hypotensives and 13 female normotensives performed a stress task followed by polysomnography. Measures derived from blood pressure monitoring, impedance cardiography, and heart rate variability were collected. Hypotensives exhibited lower cardiovascular and autonomic activation than controls during the task. While a better sleep quality (i.e., higher sleep efficiency and lower nocturnal wakefulness) correlated with a reduced reactivity in normotensives, the opposite pattern occurred in hypotensives. The results suggest that a blunted response in both autonomic branches underlies the cardiovascular hypoactivation in hypotension. Further, good sleep seems to be associated with optimal levels of physiological reactivity.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12054" xmlns="http://purl.org/rss/1.0/"><title>The effect of acute mental stress on limb vasodilation is unrelated to total peripheral resistance</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12054</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The effect of acute mental stress on limb vasodilation is unrelated to total peripheral resistance</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nicola J. Paine, Christopher Ring, Jos A. Bosch, David McIntyre, Jet J. C. S. Veldhuijzen van Zanten</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-08T21:23:52.740387-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12054</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12054</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12054</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Mental stress can trigger myocardial infarction, with poor vascular responses to stress implicated as a pathway. Vascular stress reactivity can be assessed by different methods, such as total peripheral resistance (TPR) and forearm blood flow (FBF). Little is known about how these vascular assessments are linked. This was examined in two separate studies. Healthy men (Study 1: <em>N</em> = 29, Study 2: <em>N</em> = 23) completed rest and mental arithmetic (Study 1: 8 min, Study 2: 16 min). In both studies, heart rate, mean arterial pressure, and FBF increased in response to stress. In Study 1, no changes in TPR were seen, but Study 2 found stress-induced increases in TPR. FBF was not linked to TPR at any time (all <em>p</em>s<em> &gt;</em> .05). It appears that limb vasculature and TPR responses to stress do not give the same information about impairments of the vasculature. These findings are relevant to the interpretation of prior research findings and the design of future studies on stress and vascular responses.</p></div>
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Mental stress can trigger myocardial infarction, with poor vascular responses to stress implicated as a pathway. Vascular stress reactivity can be assessed by different methods, such as total peripheral resistance (TPR) and forearm blood flow (FBF). Little is known about how these vascular assessments are linked. This was examined in two separate studies. Healthy men (Study 1: N = 29, Study 2: N = 23) completed rest and mental arithmetic (Study 1: 8 min, Study 2: 16 min). In both studies, heart rate, mean arterial pressure, and FBF increased in response to stress. In Study 1, no changes in TPR were seen, but Study 2 found stress-induced increases in TPR. FBF was not linked to TPR at any time (all ps &gt; .05). It appears that limb vasculature and TPR responses to stress do not give the same information about impairments of the vasculature. These findings are relevant to the interpretation of prior research findings and the design of future studies on stress and vascular responses.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12053" xmlns="http://purl.org/rss/1.0/"><title>Self-report and behavioral measures of reward sensitivity predict the feedback negativity</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12053</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Self-report and behavioral measures of reward sensitivity predict the feedback negativity</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jennifer N. Bress, Greg Hajcak</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-08T21:23:42.411119-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12053</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12053</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12053</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Rewards are integral to learning associations that aid in survival. The feedback negativity (FN), an event-related potential that differentiates outcomes indicating monetary losses versus gains, has recently emerged as a possible neural measure of reward processing. If this view is correct, then the FN should correlate with measures of reward sensitivity in other domains, although few studies have investigated this question. In the current study, 46 participants completed a self-report measure of reward responsiveness, a signal detection task that generated a behavioral measure of reward sensitivity, and a gambling task that elicited an FN. Consistent with the view that the FN reflects reward-related neural activity, a larger FN correlated with increased behavioral and self-report measures of sensitivity to reward.</p></div>
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Rewards are integral to learning associations that aid in survival. The feedback negativity (FN), an event-related potential that differentiates outcomes indicating monetary losses versus gains, has recently emerged as a possible neural measure of reward processing. If this view is correct, then the FN should correlate with measures of reward sensitivity in other domains, although few studies have investigated this question. In the current study, 46 participants completed a self-report measure of reward responsiveness, a signal detection task that generated a behavioral measure of reward sensitivity, and a gambling task that elicited an FN. Consistent with the view that the FN reflects reward-related neural activity, a larger FN correlated with increased behavioral and self-report measures of sensitivity to reward.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12051" xmlns="http://purl.org/rss/1.0/"><title>Cardiac defense in response to imminent threat in women with multiple trauma and severe PTSD</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12051</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cardiac defense in response to imminent threat in women with multiple trauma and severe PTSD</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">I. Schalinski, T. R. Elbert, M. Schauer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-08T21:23:31.219159-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12051</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12051</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12051</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Posttraumatic stress disorder (PTSD) arises as a long-term result of exposure to trauma and brings with it an altered autonomic response to potentially threatening stimuli. The present study investigates the dynamic sequence of cardiac defense in women with and without PTSD. An acoustic noise of 0.5-s duration and 105 dB was used to elicit the cardiac defense reaction. The stimulus was repeated three times. Within the PTSD sample, respondents who suffered from more severe PTSD showed a higher heart rate at rest, a higher baseline, and a greater response. Compared to the healthy subjects, the PTSD group showed an elevated heart rate from 6 s to 25 s following the presentation of the first stimulus. There was evidence of habituation in the PTSD group and hints of differential effects on the cardiac defense of traumatic experiences with a high proximity of danger.</p></div>
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Posttraumatic stress disorder (PTSD) arises as a long-term result of exposure to trauma and brings with it an altered autonomic response to potentially threatening stimuli. The present study investigates the dynamic sequence of cardiac defense in women with and without PTSD. An acoustic noise of 0.5-s duration and 105 dB was used to elicit the cardiac defense reaction. The stimulus was repeated three times. Within the PTSD sample, respondents who suffered from more severe PTSD showed a higher heart rate at rest, a higher baseline, and a greater response. Compared to the healthy subjects, the PTSD group showed an elevated heart rate from 6 s to 25 s following the presentation of the first stimulus. There was evidence of habituation in the PTSD group and hints of differential effects on the cardiac defense of traumatic experiences with a high proximity of danger.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12045" xmlns="http://purl.org/rss/1.0/"><title>Association between P3 event-related potential amplitude and externalizing disorders: A time-domain and time-frequency investigation of 29-year-old adults</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12045</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Association between P3 event-related potential amplitude and externalizing disorders: A time-domain and time-frequency investigation of 29-year-old adults</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Henry H. Yoon, Stephen M. Malone, Scott J. Burwell, Edward M. Bernat, William G. Iacono</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-25T02:51:00.008578-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12045</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12045</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12045</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study determined whether time-domain P3 amplitude and time-frequency principal component (TF-PC) reductions are present in adulthood (age 29) when participants have largely passed through the age of heaviest substance misuse. Participants were assessed from age 17 through 29 for lifetime externalizing (EXT) disorders. EEG comparisons from three topographic regions were examined for P3 amplitude and TF-PCs at delta and theta frequency ranges. Significant P3 amplitude reductions were found in those with EXT for both regional and site-Pz analyses, with stronger effects observed the greater the EXT comorbidity. Reductions were also observed in all eight TF-PCs extracted, with a delta component yielding frontal effects not apparent in the time domain. Overall, results suggest that these brain measures continue, at age 29, to provide effective indices of EXT that potentially tap a neural substrate related to behavioral disinhibition.</p></div>
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This study determined whether time-domain P3 amplitude and time-frequency principal component (TF-PC) reductions are present in adulthood (age 29) when participants have largely passed through the age of heaviest substance misuse. Participants were assessed from age 17 through 29 for lifetime externalizing (EXT) disorders. EEG comparisons from three topographic regions were examined for P3 amplitude and TF-PCs at delta and theta frequency ranges. Significant P3 amplitude reductions were found in those with EXT for both regional and site-Pz analyses, with stronger effects observed the greater the EXT comorbidity. Reductions were also observed in all eight TF-PCs extracted, with a delta component yielding frontal effects not apparent in the time domain. Overall, results suggest that these brain measures continue, at age 29, to provide effective indices of EXT that potentially tap a neural substrate related to behavioral disinhibition.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12044" xmlns="http://purl.org/rss/1.0/"><title>Mu suppression as an indicator of activation of the perceptual-motor system by smoking-related cues in smokers</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12044</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Mu suppression as an indicator of activation of the perceptual-motor system by smoking-related cues in smokers</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Cheryl L. Dickter, Paul D. Kieffaber, Julie A. Kittel, Catherine A. Forestell</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-15T02:16:12.350493-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12044</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12044</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12044</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The goal of the current study was to determine whether activation of the mirror neuron system, as measured by mu rhythm desynchronization, varied as a function of image content in smokers compared with nonsmokers. EEG activity was recorded while participants passively viewed images depicting smoking-related and nonsmoking-related stimuli. In half of the images, cues were depicted alone (inactive), while for the remaining images, cues were depicted with humans interacting with them (active). For the nonsmoking stimuli, smokers and nonsmokers showed greater mu suppression to the active cues compared to the inactive cues. However, for the smoking-related stimuli, smokers showed greater perception-action coupling for the active cues as reflected in their enhanced mu suppression, compared to nonsmokers. The results of the current study support the involvement of the perceptual-motor system in the activation of motivated drug use behaviors.</p></div>
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The goal of the current study was to determine whether activation of the mirror neuron system, as measured by mu rhythm desynchronization, varied as a function of image content in smokers compared with nonsmokers. EEG activity was recorded while participants passively viewed images depicting smoking-related and nonsmoking-related stimuli. In half of the images, cues were depicted alone (inactive), while for the remaining images, cues were depicted with humans interacting with them (active). For the nonsmoking stimuli, smokers and nonsmokers showed greater mu suppression to the active cues compared to the inactive cues. However, for the smoking-related stimuli, smokers showed greater perception-action coupling for the active cues as reflected in their enhanced mu suppression, compared to nonsmokers. The results of the current study support the involvement of the perceptual-motor system in the activation of motivated drug use behaviors.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12047" xmlns="http://purl.org/rss/1.0/"><title>Variance stabilization for computing and comparing grand mean waveforms in MEG and EEG</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12047</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Variance stabilization for computing and comparing grand mean waveforms in MEG and EEG</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Artur Matysiak, Wojciech Kordecki, Cezary Sielużycki, Norman Zacharias, Peter Heil, Reinhard König</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-12T04:07:47.328312-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12047</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12047</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12047</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Grand means of time-varying signals (waveforms) across subjects in magnetoencephalography (MEG) and electroencephalography (EEG) are commonly computed as arithmetic averages and compared between conditions, for example, by subtraction. However, the prerequisite for these operations, homogeneity of the variance of the waveforms in time, and for most common parametric statistical tests also between conditions, is rarely met. We suggest that the heteroscedasticity observed instead results because waveforms may differ by factors and additive terms and follow a mixed model. We propose to apply the asinh-transformation to stabilize the variance in such cases. We demonstrate the homogeneous variance and the normal distributions of data achieved by this transformation using simulated waveforms, and we apply it to real MEG data and show its benefits. The asinh-transformation is thus an essential and useful processing step prior to computing and comparing grand mean waveforms in MEG and EEG.</p></div>
]]></content:encoded><description>

Grand means of time-varying signals (waveforms) across subjects in magnetoencephalography (MEG) and electroencephalography (EEG) are commonly computed as arithmetic averages and compared between conditions, for example, by subtraction. However, the prerequisite for these operations, homogeneity of the variance of the waveforms in time, and for most common parametric statistical tests also between conditions, is rarely met. We suggest that the heteroscedasticity observed instead results because waveforms may differ by factors and additive terms and follow a mixed model. We propose to apply the asinh-transformation to stabilize the variance in such cases. We demonstrate the homogeneous variance and the normal distributions of data achieved by this transformation using simulated waveforms, and we apply it to real MEG data and show its benefits. The asinh-transformation is thus an essential and useful processing step prior to computing and comparing grand mean waveforms in MEG and EEG.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12050" xmlns="http://purl.org/rss/1.0/"><title>The “red-alert” effect in visual search: Evidence from human electrophysiology</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12050</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The “red-alert” effect in visual search: Evidence from human electrophysiology</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ulysse Fortier-Gauthier, Roberto Dell'Acqua, Pierre Jolicœur</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-12T04:07:35.15418-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12050</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12050</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12050</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Participants had to determine the orientation of a segment inside a target color circle among other gray distractor circles. The target circle was either red or green and was accompanied in the display by a distractor in the other color. To dissociate event-related potentials of target and distractor processing, one of them was on the vertical meridian and the other in a lateral position. In Experiment 1, the target color was indicated on a per-trial basis and, in Experiment 2, on a per-block basis. The results revealed the N2pc elicited by red targets had an earlier latency relative to the N2pc elicited by green targets. Contralateral responses of positive polarity linked to distractor inhibition were found only with red lateral distractors. The results suggest that the choice of colors to distinguish targets from distractors may play a role in visual search performance and in the functional characterization of event-related lateralizations.</p></div>
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Participants had to determine the orientation of a segment inside a target color circle among other gray distractor circles. The target circle was either red or green and was accompanied in the display by a distractor in the other color. To dissociate event-related potentials of target and distractor processing, one of them was on the vertical meridian and the other in a lateral position. In Experiment 1, the target color was indicated on a per-trial basis and, in Experiment 2, on a per-block basis. The results revealed the N2pc elicited by red targets had an earlier latency relative to the N2pc elicited by green targets. Contralateral responses of positive polarity linked to distractor inhibition were found only with red lateral distractors. The results suggest that the choice of colors to distinguish targets from distractors may play a role in visual search performance and in the functional characterization of event-related lateralizations.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12048" xmlns="http://purl.org/rss/1.0/"><title>Separating mismatch negativity (MMN) response from auditory obligatory brain responses in school-aged children</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12048</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Separating mismatch negativity (MMN) response from auditory obligatory brain responses in school-aged children</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kaisa Lohvansuu, Jarmo A. Hämäläinen, Annika Tanskanen, Jürgen Bartling, Jennifer Bruder, Ferenc Honbolygó, Gerd Schulte-Körne, Jean-Francois Démonet, Valéria Csépe, Paavo H. T. Leppänen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-12T04:07:32.022228-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12048</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12048</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12048</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Mismatch negativity (MMN) overlaps with other auditory event-related potential (ERP) components. We examined the ERPs of 50 9- to 11-year-old children for vowels /i/, /y/ and equivalent complex tones. The goal was to separate MMN from obligatory ERP components using principal component analysis and equal probability control condition. In addition to the contrast of the deviant minus standard response, we employed the contrast of the deviant minus control response, to see whether the obligatory processing contributes to MMN in children. When looking for differences in speech deviant minus standard contrast, MMN starts around 112 ms. However, when both contrasts are examined, MMN emerges for speech at 160 ms whereas for nonspeech MMN is observed at 112 ms regardless of contrast. We argue that this discriminative response to speech stimuli at 112 ms is obligatory in nature rather than reflecting change detection processing.</p></div>
]]></content:encoded><description>

Mismatch negativity (MMN) overlaps with other auditory event-related potential (ERP) components. We examined the ERPs of 50 9- to 11-year-old children for vowels /i/, /y/ and equivalent complex tones. The goal was to separate MMN from obligatory ERP components using principal component analysis and equal probability control condition. In addition to the contrast of the deviant minus standard response, we employed the contrast of the deviant minus control response, to see whether the obligatory processing contributes to MMN in children. When looking for differences in speech deviant minus standard contrast, MMN starts around 112 ms. However, when both contrasts are examined, MMN emerges for speech at 160 ms whereas for nonspeech MMN is observed at 112 ms regardless of contrast. We argue that this discriminative response to speech stimuli at 112 ms is obligatory in nature rather than reflecting change detection processing.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12046" xmlns="http://purl.org/rss/1.0/"><title>Identifying concealment-related responses in the concealed information test</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12046</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Identifying concealment-related responses in the concealed information test</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Izumi Matsuda, Hiroshi Nittono, Tokihiro Ogawa</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-08T06:30:23.413044-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12046</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12046</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12046</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The concealed information test (CIT) assesses an examinee's recognition of a crime-relevant item using physiological measures. However, a guilty examinee not only recognizes the crime-relevant item but also conceals the recognition intentionally. In this study, we attempted to identify the effect of concealing the recognition on event-related potentials and autonomic responses. After committing a mock theft of two items, 30 participants received two CITs: one for an item that they had to conceal, and the other for an item that they had disclosed. N2, P3, heart rate, skin conductance, and cutaneous blood flow differed between crime-relevant and irrelevant items in both CITs. In contrast, late positive potential and respiration differed between crime-relevant and irrelevant items only when the examinee needed to conceal. The former measures appear to be related to orienting process, whereas the latter to controlled process related to concealment.</p></div>
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The concealed information test (CIT) assesses an examinee's recognition of a crime-relevant item using physiological measures. However, a guilty examinee not only recognizes the crime-relevant item but also conceals the recognition intentionally. In this study, we attempted to identify the effect of concealing the recognition on event-related potentials and autonomic responses. After committing a mock theft of two items, 30 participants received two CITs: one for an item that they had to conceal, and the other for an item that they had disclosed. N2, P3, heart rate, skin conductance, and cutaneous blood flow differed between crime-relevant and irrelevant items in both CITs. In contrast, late positive potential and respiration differed between crime-relevant and irrelevant items only when the examinee needed to conceal. The former measures appear to be related to orienting process, whereas the latter to controlled process related to concealment.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1469-8986.2011.1208.x" xmlns="http://purl.org/rss/1.0/"><title>Implementing conditional inference in the auditory system: What matters?</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1469-8986.2011.1208.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Implementing conditional inference in the auditory system: What matters?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Juanita Todd, Daniel Mullens</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-04-05T07:29:09.806479-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1469-8986.2011.1208.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1469-8986.2011.1208.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1469-8986.2011.1208.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In prior studies, we have used a conditional linkage between rare deviations in a regular sound pattern to determine if the auditory system can use the first deviation to anticipate the probable features of the second deviation (i.e., make a conditional inference). This study was designed to test two hypotheses about why the mismatch negativity (MMN) to a duration deviant sound seems more susceptible to conditional inference effects. The MMNs to duration and frequency glide deviant sounds were significantly smaller when their occurrence was conditionally linked to the identity of a prior deviant as opposed to when they occurred randomly in a sequence. Results provide support for the learned conditional inference interpretation of reduced MMN size to linked deviants. We discuss alternate explanations and conclude that conditional inference studies could provide insight into the dynamics of probability-based prediction in the auditory system.</p></div>]]></content:encoded><description>In prior studies, we have used a conditional linkage between rare deviations in a regular sound pattern to determine if the auditory system can use the first deviation to anticipate the probable features of the second deviation (i.e., make a conditional inference). This study was designed to test two hypotheses about why the mismatch negativity (MMN) to a duration deviant sound seems more susceptible to conditional inference effects. The MMNs to duration and frequency glide deviant sounds were significantly smaller when their occurrence was conditionally linked to the identity of a prior deviant as opposed to when they occurred randomly in a sequence. Results provide support for the learned conditional inference interpretation of reduced MMN size to linked deviants. We discuss alternate explanations and conclude that conditional inference studies could provide insight into the dynamics of probability-based prediction in the auditory system.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1469-8986.2011.1202.x" xmlns="http://purl.org/rss/1.0/"><title>Electrophysiological correlates of decision-making in high-risk versus low-risk conditions of a gambling game</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1469-8986.2011.1202.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Electrophysiological correlates of decision-making in high-risk versus low-risk conditions of a gambling game</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Juan Yang, Qinglin Zhang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-04-05T07:28:28.279846-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1469-8986.2011.1202.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1469-8986.2011.1202.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1469-8986.2011.1202.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The majority of studies investigating risky decision making focus on the high-conflict condition, and very few consider the low-conflict condition in which there is either a very high or a very low probability of risk. Even though the high-risk condition and low-risk condition are both considered low-conflict decision scenarios and both behavioral outcomes are highly predictable, these conditions still differ in terms of the probabilities of reward and punishment. In the following study, we investigated both behavioral and electrophysiological correlates associated with high- and low-risk conditions within the low-conflict scenario, as well as high-conflict condition, in a modified gambling game. The behavioral results showed that, within the low-conflict scenario, the participants took more time to make the decision in the high-risk condition compared to the low-risk condition. The event-related potentials (ERP) data showed that, during the decision making, the high-risk condition evoked a more negative ERP deflection than did the low-risk condition in the time window of 300–500 ms (N400), which had a frontocentral focus of scalp distribution. The results suggested that the high-risk condition was associated with a higher conflict between the participants' “motivationally based” tendency to want to receive cards and the task instructions, which stated that the face value of the first two cards will strongly predict a low probability of success. It was further speculated that the N400 in the present study might be associated with anticipation of negative rewards, which was functionally equivalent to the FRN (feedback-related negativity) to negative outcomes.</p></div>]]></content:encoded><description>The majority of studies investigating risky decision making focus on the high-conflict condition, and very few consider the low-conflict condition in which there is either a very high or a very low probability of risk. Even though the high-risk condition and low-risk condition are both considered low-conflict decision scenarios and both behavioral outcomes are highly predictable, these conditions still differ in terms of the probabilities of reward and punishment. In the following study, we investigated both behavioral and electrophysiological correlates associated with high- and low-risk conditions within the low-conflict scenario, as well as high-conflict condition, in a modified gambling game. The behavioral results showed that, within the low-conflict scenario, the participants took more time to make the decision in the high-risk condition compared to the low-risk condition. The event-related potentials (ERP) data showed that, during the decision making, the high-risk condition evoked a more negative ERP deflection than did the low-risk condition in the time window of 300–500 ms (N400), which had a frontocentral focus of scalp distribution. The results suggested that the high-risk condition was associated with a higher conflict between the participants' “motivationally based” tendency to want to receive cards and the task instructions, which stated that the face value of the first two cards will strongly predict a low probability of success. It was further speculated that the N400 in the present study might be associated with anticipation of negative rewards, which was functionally equivalent to the FRN (feedback-related negativity) to negative outcomes.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12039" xmlns="http://purl.org/rss/1.0/"><title>What the heart forgets: Cardiac timing influences memory for words and is modulated by metacognition and interoceptive sensitivity</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12039</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">What the heart forgets: Cardiac timing influences memory for words and is modulated by metacognition and interoceptive sensitivity</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sarah N. Garfinkel, Adam B. Barrett, Ludovico Minati, Raymond J. Dolan, Anil K. Seth, Hugo D. Critchley</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-21T23:39:23.565151-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12039</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12039</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12039</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">505</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">512</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Mental functions are influenced by states of physiological arousal. Afferent neural activity from arterial baroreceptors at systole conveys the strength and timing of individual heartbeats to the brain. We presented words under limited attentional resources time-locked to different phases of the cardiac cycle, to test a hypothesis that natural baroreceptor stimulation influences detection and subsequent memory of words. We show memory for words presented around systole was decreased relative to words at diastole. The deleterious memory effect of systole was greater for words detected with low confidence and amplified in individuals with low interoceptive sensitivity, as indexed using a heartbeat counting task. Our observations highlight an important cardiovascular channel through which autonomic arousal impacts a cognitive function, an effect mitigated by metacognition (perceptual confidence) and interoceptive sensitivity.</p></div>
]]></content:encoded><description>

Mental functions are influenced by states of physiological arousal. Afferent neural activity from arterial baroreceptors at systole conveys the strength and timing of individual heartbeats to the brain. We presented words under limited attentional resources time-locked to different phases of the cardiac cycle, to test a hypothesis that natural baroreceptor stimulation influences detection and subsequent memory of words. We show memory for words presented around systole was decreased relative to words at diastole. The deleterious memory effect of systole was greater for words detected with low confidence and amplified in individuals with low interoceptive sensitivity, as indexed using a heartbeat counting task. Our observations highlight an important cardiovascular channel through which autonomic arousal impacts a cognitive function, an effect mitigated by metacognition (perceptual confidence) and interoceptive sensitivity.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12036" xmlns="http://purl.org/rss/1.0/"><title>Blood pressure and pain sensitivity in children and adolescents</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12036</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Blood pressure and pain sensitivity in children and adolescents</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sammantha Drouin, Jennifer J. McGrath</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-20T22:14:00.735025-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12036</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12036</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12036</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">513</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">520</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Elevated blood pressure is associated with diminished pain sensitivity. While this finding is well established in adults, it is less clear when the relation between blood pressure and pain sensitivity emerges across the life course. Evidence suggests this phenomenon may exist during childhood. Children (<em>N</em> = 309; 56% boys) aged 10–15 years and their parents participated. Blood pressure readings were taken during a resting baseline. Maximum pain intensity was rated using a visual analogue scale (rated 0–10) in response to a finger prick pain induction. Parent-measured resting blood pressure was inversely associated with boys' pain ratings only. Cross-sectionally, lower pain ratings were related to higher SBP, univariately. Longitudinally, pain ratings predicted higher DBP, even after controlling for covariates. Determining when and how the relation between blood pressure and pain sensitivity emerges may elucidate the pathophysiology of hypertension.</p></div>
]]></content:encoded><description>

Elevated blood pressure is associated with diminished pain sensitivity. While this finding is well established in adults, it is less clear when the relation between blood pressure and pain sensitivity emerges across the life course. Evidence suggests this phenomenon may exist during childhood. Children (N = 309; 56% boys) aged 10–15 years and their parents participated. Blood pressure readings were taken during a resting baseline. Maximum pain intensity was rated using a visual analogue scale (rated 0–10) in response to a finger prick pain induction. Parent-measured resting blood pressure was inversely associated with boys' pain ratings only. Cross-sectionally, lower pain ratings were related to higher SBP, univariately. Longitudinally, pain ratings predicted higher DBP, even after controlling for covariates. Determining when and how the relation between blood pressure and pain sensitivity emerges may elucidate the pathophysiology of hypertension.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12038" xmlns="http://purl.org/rss/1.0/"><title>Gender differences in cardiac autonomic modulation during medical internship</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12038</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Gender differences in cardiac autonomic modulation during medical internship</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yu-Hsuan Lin, Ching-Yen Chen, Sheng-Hsuan Lin, Chun-Hao Liu, Wei-Hung Weng, Terry B. J. Kuo, Cheryl C. H. Yang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-20T22:25:31.05087-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12038</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12038</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12038</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">521</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">527</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Medical internship is known to be a time of high stress and long working hours, which increases the risk of depression and cardiovascular disease. Gender differences in medical interns' cardiovascular risk have not been reported previously. Thirty-eight medical interns (29 males) were repeatedly tested for depressive symptoms using the Hospital Anxiety and Depression Scale and 5-min spectral analysis of heart rate variability (HRV) at 3-month intervals during their internship. Among the male interns, the variance of the heart rate decreased at 6, 9, 12 months, and a reduced high frequency, which suggests reduced cardiac parasympathetic modulation, was found at 9 and 12 months into their internship. Increased depressive symptoms were also identified at 12 months in the male group. No significant differences in depression or any of the HRV indices were identified among the female interns during their internship.</p></div>
]]></content:encoded><description>

Medical internship is known to be a time of high stress and long working hours, which increases the risk of depression and cardiovascular disease. Gender differences in medical interns' cardiovascular risk have not been reported previously. Thirty-eight medical interns (29 males) were repeatedly tested for depressive symptoms using the Hospital Anxiety and Depression Scale and 5-min spectral analysis of heart rate variability (HRV) at 3-month intervals during their internship. Among the male interns, the variance of the heart rate decreased at 6, 9, 12 months, and a reduced high frequency, which suggests reduced cardiac parasympathetic modulation, was found at 9 and 12 months into their internship. Increased depressive symptoms were also identified at 12 months in the male group. No significant differences in depression or any of the HRV indices were identified among the female interns during their internship.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12042" xmlns="http://purl.org/rss/1.0/"><title>Effects of intranasal oxytocin on pupil dilation indicate increased salience of socioaffective stimuli</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12042</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effects of intranasal oxytocin on pupil dilation indicate increased salience of socioaffective stimuli</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kristin Prehn, Philipp Kazzer, Alexander Lischke, Markus Heinrichs, Sabine C. Herpertz, Gregor Domes</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-02T23:32:19.230242-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12042</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12042</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12042</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">528</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">537</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>To investigate the mechanisms by which oxytocin improves socioaffective processing, we measured behavioral and pupillometric data during a dynamic facial emotion recognition task. In a double-blind between-subjects design, 47 men received either 24 IU intranasal oxytocin (OXT) or a placebo (PLC). Participants in the OXT group recognized all facial expressions at lower intensity levels than did participants in the PLC group. Improved performance was accompanied by increased task-related pupil dilation, indicating an increased recruitment of attentional resources. We also found increased pupil dilation during the processing of female compared with male faces. This gender-specific stimulus effect diminished in the OXT group, in which pupil size specifically increased for male faces. Results suggest that improved emotion recognition after OXT treatment might be due to an intensified processing of stimuli that usually do not recruit much attention.</p></div>
]]></content:encoded><description>

To investigate the mechanisms by which oxytocin improves socioaffective processing, we measured behavioral and pupillometric data during a dynamic facial emotion recognition task. In a double-blind between-subjects design, 47 men received either 24 IU intranasal oxytocin (OXT) or a placebo (PLC). Participants in the OXT group recognized all facial expressions at lower intensity levels than did participants in the PLC group. Improved performance was accompanied by increased task-related pupil dilation, indicating an increased recruitment of attentional resources. We also found increased pupil dilation during the processing of female compared with male faces. This gender-specific stimulus effect diminished in the OXT group, in which pupil size specifically increased for male faces. Results suggest that improved emotion recognition after OXT treatment might be due to an intensified processing of stimuli that usually do not recruit much attention.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12035" xmlns="http://purl.org/rss/1.0/"><title>Positive and negative affect in adolescent self-evaluation: Psychometric information in single trials used to generate dimension-specific ERPs and neural source models</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12035</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Positive and negative affect in adolescent self-evaluation: Psychometric information in single trials used to generate dimension-specific ERPs and neural source models</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Allison C. Waters, Don M. Tucker</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-11T07:57:04.87283-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12035</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12035</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12035</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">538</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">549</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We examined brain mechanisms of self-evaluation in a sample of adolescents using dense array EEG (dEEG), neural source analysis, and a novel psychometric weighting method. Each trial of the self-evaluation task was weighted according to its correlation with negative affect and positive affect, such that unique ERP averages were constructed for each mood dimension. Results support the hypothesis that the emotional influence on self-appraisal is dimension specific. Negative affect was associated with more robust ERP responses 300 ms into the decision-making epoch. Affect-weighted source analyses further differentiated dorsal-posterior and ventral-anterior features of brain activity. The integration of psychometric weights and dEEG neural source analysis may provide new clues to the neural mechanisms of affective influence on self-evaluative cognition.</p></div>
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We examined brain mechanisms of self-evaluation in a sample of adolescents using dense array EEG (dEEG), neural source analysis, and a novel psychometric weighting method. Each trial of the self-evaluation task was weighted according to its correlation with negative affect and positive affect, such that unique ERP averages were constructed for each mood dimension. Results support the hypothesis that the emotional influence on self-appraisal is dimension specific. Negative affect was associated with more robust ERP responses 300 ms into the decision-making epoch. Affect-weighted source analyses further differentiated dorsal-posterior and ventral-anterior features of brain activity. The integration of psychometric weights and dEEG neural source analysis may provide new clues to the neural mechanisms of affective influence on self-evaluative cognition.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12040" xmlns="http://purl.org/rss/1.0/"><title>Frontal midline theta and N200 amplitude reflect complementary information about expectancy and outcome evaluation</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12040</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Frontal midline theta and N200 amplitude reflect complementary information about expectancy and outcome evaluation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Azadeh Hajihosseini, Clay B. Holroyd</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-21T23:39:30.398498-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12040</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12040</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12040</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">550</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">562</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Feedback ERN (fERN) and frontal midline theta have both been proposed to index a dopamine-like reinforcement learning signal in anterior cingulate cortex (ACC). We investigated these proposals by comparing fERN amplitude and theta power with respect to their sensitivities to outcome valence and probability in a previously collected EEG dataset. Bayesian model comparison revealed a dissociation between the two measures, with fERN amplitude mainly sensitive to valence and theta power mainly sensitive to probability. Further, fERN amplitude was highly correlated with the portion of theta power that is consistent in phase across trials (i.e., evoked theta power). These results suggest that although both measures provide valuable information about cognitive function of frontal midline cortex, fERN amplitude is specifically sensitive to dopamine reinforcement learning signals whereas theta power reflects the ACC response to unexpected events.</p></div>
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Feedback ERN (fERN) and frontal midline theta have both been proposed to index a dopamine-like reinforcement learning signal in anterior cingulate cortex (ACC). We investigated these proposals by comparing fERN amplitude and theta power with respect to their sensitivities to outcome valence and probability in a previously collected EEG dataset. Bayesian model comparison revealed a dissociation between the two measures, with fERN amplitude mainly sensitive to valence and theta power mainly sensitive to probability. Further, fERN amplitude was highly correlated with the portion of theta power that is consistent in phase across trials (i.e., evoked theta power). These results suggest that although both measures provide valuable information about cognitive function of frontal midline cortex, fERN amplitude is specifically sensitive to dopamine reinforcement learning signals whereas theta power reflects the ACC response to unexpected events.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12041" xmlns="http://purl.org/rss/1.0/"><title>No evidence for peripheral mechanism attenuating auditory ERPs to self-induced tones</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12041</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">No evidence for peripheral mechanism attenuating auditory ERPs to self-induced tones</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">János Horváth, Annamária Burgyán</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-28T23:19:07.16001-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12041</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12041</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12041</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">563</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">569</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The N1 and P2 event-related potentials (ERPs) are attenuated when the eliciting sounds coincide with our own actions. Although this ERP attenuation could be caused by central processes, it may also reflect a peripheral mechanism: the coactivation of the stapedius muscle with the task-relevant effector, which reduces signal transmission efficiency in the middle ear, reducing the effective intensity of concurrently presented tones, which, in turn, elicit lower amplitude auditory ERPs. Because stapedius muscle contraction attenuates frequencies below 2 kHz, no attenuation should occur at frequencies above 2 kHz. A self-induced tone paradigm was administered with 0.5, 2.0, and 8.0 kHz pure tones. Self-induced tones elicited attenuated N1 and P2 ERPs, but the magnitude of attenuation was not affected by tone frequency. This result does not support the hypothesis that ERP attenuation to self-induced tones are caused by stapedius muscle contractions.</p></div>
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The N1 and P2 event-related potentials (ERPs) are attenuated when the eliciting sounds coincide with our own actions. Although this ERP attenuation could be caused by central processes, it may also reflect a peripheral mechanism: the coactivation of the stapedius muscle with the task-relevant effector, which reduces signal transmission efficiency in the middle ear, reducing the effective intensity of concurrently presented tones, which, in turn, elicit lower amplitude auditory ERPs. Because stapedius muscle contraction attenuates frequencies below 2 kHz, no attenuation should occur at frequencies above 2 kHz. A self-induced tone paradigm was administered with 0.5, 2.0, and 8.0 kHz pure tones. Self-induced tones elicited attenuated N1 and P2 ERPs, but the magnitude of attenuation was not affected by tone frequency. This result does not support the hypothesis that ERP attenuation to self-induced tones are caused by stapedius muscle contractions.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12043" xmlns="http://purl.org/rss/1.0/"><title>Peak individual alpha frequency qualifies as a stable neurophysiological trait marker in healthy younger and older adults</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12043</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Peak individual alpha frequency qualifies as a stable neurophysiological trait marker in healthy younger and older adults</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Thomas H. Grandy, Markus Werkle-Bergner, Christian Chicherio, Florian Schmiedek, Martin Lövdén, Ulman Lindenberger</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-02T23:32:23.865207-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12043</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12043</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12043</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">570</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">582</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The individual alpha frequency (IAF) of the human EEG reflects systemic properties of the brain, is highly heritable, and relates to cognitive functioning. Not much is known about the modifiability of IAF by cognitive interventions. We report analyses of resting EEG from a large-scale training study in which healthy younger (20–31 years, <em>N</em> = 30) and older (65–80 years, <em>N</em> = 28) adults practiced 12 cognitive tasks for ∼100 1-h sessions. EEG was recorded before and after the cognitive training intervention. In both age groups, IAF (and, in a control analysis, alpha amplitude) did not change, despite large gains in cognitive performance. As within-session reliability and test-retest stability were high for both age groups, imprecise measurements cannot account for the findings. In sum, IAF is highly stable in healthy adults up to 80 years, not easily modifiable by cognitive interventions alone, and thus qualifies as a stable neurophysiological trait marker.</p></div>
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The individual alpha frequency (IAF) of the human EEG reflects systemic properties of the brain, is highly heritable, and relates to cognitive functioning. Not much is known about the modifiability of IAF by cognitive interventions. We report analyses of resting EEG from a large-scale training study in which healthy younger (20–31 years, N = 30) and older (65–80 years, N = 28) adults practiced 12 cognitive tasks for ∼100 1-h sessions. EEG was recorded before and after the cognitive training intervention. In both age groups, IAF (and, in a control analysis, alpha amplitude) did not change, despite large gains in cognitive performance. As within-session reliability and test-retest stability were high for both age groups, imprecise measurements cannot account for the findings. In sum, IAF is highly stable in healthy adults up to 80 years, not easily modifiable by cognitive interventions alone, and thus qualifies as a stable neurophysiological trait marker.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12037" xmlns="http://purl.org/rss/1.0/"><title>A parietal-to-frontal shift in the P300 is associated with compensation of tactile discrimination deficits in late middle-aged adults</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12037</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A parietal-to-frontal shift in the P300 is associated with compensation of tactile discrimination deficits in late middle-aged adults</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Eva-Maria Reuter, Claudia Voelcker-Rehage, Solveig Vieluf, Axel H. Winneke, Ben Godde</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-20T22:14:25.404135-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/psyp.12037</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/psyp.12037</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fpsyp.12037</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">583</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">593</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Tactile perception declines with age on both behavioral and neurophysiological levels. Less well understood is how neurophysiological changes relate to tactile discrimination performance in middle adulthood. A tactile discrimination task was conducted while ERPs were measured in three groups of healthy adults aged 20 to 66 years. Accuracy was lowest in late middle adulthood (56–66 years) while somatosensory ERP components (P50, N70, P100, N140) were comparable across age groups. The cognitive P300 revealed age-related differences in scalp distribution typical for older adults to already be present in late middle adulthood. Increased recruitment of frontal cognitive processes was positively related to performance in later middle adulthood. Our results further the understanding of age-related differences in tactile perception during middle adulthood and the importance of cognitive processes to compensate for age-related decline.</p></div>
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Tactile perception declines with age on both behavioral and neurophysiological levels. Less well understood is how neurophysiological changes relate to tactile discrimination performance in middle adulthood. A tactile discrimination task was conducted while ERPs were measured in three groups of healthy adults aged 20 to 66 years. Accuracy was lowest in late middle adulthood (56–66 years) while somatosensory ERP components (P50, N70, P100, N140) were comparable across age groups. The cognitive P300 revealed age-related differences in scalp distribution typical for older adults to already be present in late middle adulthood. Increased recruitment of frontal cognitive processes was positively related to performance in later middle adulthood. Our results further the understanding of age-related differences in tactile perception during middle adulthood and the importance of cognitive processes to compensate for age-related decline.
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