scholarly journals Common-onset Visual Masking in Infancy: Behavioral and Electrophysiological Evidence

2006 ◽  
Vol 18 (6) ◽  
pp. 966-973 ◽  
Author(s):  
Eleni Kotsoni ◽  
Denis Mareschal ◽  
Gergely Csibra ◽  
Mark H. Johnson

Common-onset visual masking (COVM) occurs when a mask and a target have common onset but delayed offset, with the mask persisting beyond the duration of the target [Di Lollo, V., Enns, J. T., & Rensink, R. A. Competition for consciousness among visual events: The psychophysics of reentrant visual events. Journal of Experimental Psychology: General, 129, 481–507, 2000]. We report the first behavioral and electrophysiological evidence of COVM in infants. An initial behavioral study included a familiarization phase during which a visual pattern (the target) surrounded by four black dots (the mask) was flashed 15 times to the infant. In the “unmasked” condition, the mask disappeared with the target. In the “masked” condition, the mask remained on the screen after deletion of the target for a further 93 msec. During the test phase, the familiar target pattern was paired with a new pattern. Infants in the unmasked condition showed a significant familiarity preference, suggesting that they had encoded the target during familiarization, whereas those in the masked condition showed no preference, suggesting that they had not encoded the target during familiarization. In the second experiment, high-density event-related potentials were used to investigate the electrophysiological pattern of activity that accompanies COVM. Six-month-old infants viewed both masked and unmasked conditions. Electrophysiological data indicated that over posterior channels the masked condition elicited a larger amplitude positive wave around 300 msec after stimulus onset than trials in the unmasked condition.

2010 ◽  
Vol 22 (1) ◽  
pp. 124-138 ◽  
Author(s):  
Todd C. Handy ◽  
Daniel Smilek ◽  
Lena Geiger ◽  
Cindy Liu ◽  
Jonathan W. Schooler

We know that human neurocognitive systems rapidly and implicitly evaluate emotionally charged stimuli. But what about more everyday, frequently encountered kinds of objects, such as computer desktop icons and business logos? Do we rapidly and implicitly evaluate these more prosaic visual images, attitude objects that might only engender a mild sense of liking or disliking, if at all? To address this question, we asked participants to view a set of unfamiliar commercial logos in the context of a target identification task as brain electrical responses to these objects were recorded via event-related potentials (ERPs). Following this task, participants individually identified those logos that were most liked or disliked, allowing us to then compare how ERP responses to logos varied as a function of hedonic evaluation—a procedure decoupling evaluative responses from any normative classification of the logos themselves. In Experiment 1, we found that visuocortical processing manifest a specific bias for disliked logos that emerged within the first 200 msec of stimulus onset. In Experiment 2, we replicated this effect while dissociating normative- and novelty-related influences. Taken together, our results provide direct electrophysiological evidence suggesting that we rapidly and implicitly evaluate commercial branding images at a hedonic level.


2010 ◽  
Vol 24 (3) ◽  
pp. 198-209 ◽  
Author(s):  
Yan Wang ◽  
Jianhui Wu ◽  
Shimin Fu ◽  
Yuejia Luo

In the present study, we used event-related potentials (ERPs) and behavioral measurements in a peripherally cued line-orientation discrimination task to investigate the underlying mechanisms of orienting and focusing in voluntary and involuntary attention conditions. Informative peripheral cue (75% valid) with long stimulus onset asynchrony (SOA) was used in the voluntary attention condition; uninformative peripheral cue (50% valid) with short SOA was used in the involuntary attention condition. Both orienting and focusing were affected by attention type. Results for attention orienting in the voluntary attention condition confirmed the “sensory gain control theory,” as attention enhanced the amplitude of the early ERP components, P1 and N1, without latency changes. In the involuntary attention condition, compared with invalid trials, targets in the valid trials elicited larger and later contralateral P1 components, and smaller and later contralateral N1 components. Furthermore, but only in the voluntary attention condition, targets in the valid trials elicited larger N2 and P3 components than in the invalid trials. Attention focusing in the involuntary attention condition resulted in larger P1 components elicited by targets in small-cue trials compared to large-cue trials, whereas in the voluntary attention condition, larger P1 components were elicited by targets in large-cue trials than in small-cue trials. There was no interaction between orienting and focusing. These results suggest that orienting and focusing of visual-spatial attention are deployed independently regardless of attention type. In addition, the present results provide evidence of dissociation between voluntary and involuntary attention during the same task.


2015 ◽  
Vol 114 (5) ◽  
pp. 2672-2681 ◽  
Author(s):  
Emanuel N. van den Broeke ◽  
André Mouraux ◽  
Antonia H. Groneberg ◽  
Doreen B. Pfau ◽  
Rolf-Detlef Treede ◽  
...  

Secondary hyperalgesia is believed to be a key feature of “central sensitization” and is characterized by enhanced pain to mechanical nociceptive stimuli. The aim of the present study was to characterize, using EEG, the effects of pinprick stimulation intensity on the magnitude of pinprick-elicited brain potentials [event-related potentials (ERPs)] before and after secondary hyperalgesia induced by intradermal capsaicin in humans. Pinprick-elicited ERPs and pinprick-evoked pain ratings were recorded in 19 healthy volunteers, with mechanical pinprick stimuli of varying intensities (0.25-mm probe applied with a force extending between 16 and 512 mN). The recordings were performed before (T0) and 30 min after (T1) intradermal capsaicin injection. The contralateral noninjected arm served as control. ERPs elicited by stimulation of untreated skin were characterized by 1) an early-latency negative-positive complex peaking between 120 and 250 ms after stimulus onset (N120-P240) and maximal at the vertex and 2) a long-lasting positive wave peaking 400–600 ms after stimulus onset and maximal more posterior (P500), which was correlated to perceived pinprick pain. After capsaicin injection, pinprick stimuli were perceived as more intense in the area of secondary hyperalgesia and this effect was stronger for lower compared with higher stimulus intensities. In addition, there was an enhancement of the P500 elicited by stimuli of intermediate intensity, which was significant for 64 mN. The other components of the ERPs were unaffected by capsaicin. Our results suggest that the increase in P500 magnitude after capsaicin is mediated by facilitated mechanical nociceptive pathways.


2009 ◽  
Vol 21 (1) ◽  
pp. 93-104 ◽  
Author(s):  
Redmond G. O'Connell ◽  
Paul M. Dockree ◽  
Mark A. Bellgrove ◽  
Alessandra Turin ◽  
Seamus Ward ◽  
...  

Disentangling the component processes that contribute to human executive control is a key challenge for cognitive neuroscience. Here, we employ event-related potentials to provide electrophysiological evidence that action errors during a go/no-go task can result either from sustained attention failures or from failures of response inhibition, and that these two processes are temporally and physiologically dissociable, although the behavioral error—a nonintended response—is the same. Thirteen right-handed participants performed a version of a go/no-go task in which stimuli were presented in a fixed and predictable order, thus encouraging attentional drift, and a second version in which an identical set of stimuli was presented in a random order, thus placing greater emphasis on response inhibition. Electrocortical markers associated with goal maintenance (late positivity, alpha synchronization) distinguished correct and incorrect performance in the fixed condition, whereas errors in the random condition were linked to a diminished N2–P3 inhibitory complex. In addition, the amplitude of the error-related negativity did not differ between correct and incorrect responses in the fixed condition, consistent with the view that errors in this condition do not arise from a failure to resolve response competition. Our data provide an electrophysiological dissociation of sustained attention and response inhibition.


2020 ◽  
Vol 8 (3-4) ◽  
pp. 254-278
Author(s):  
Lisa V. Eberhardt ◽  
Ferdinand Pittino ◽  
Anna Scheins ◽  
Anke Huckauf ◽  
Markus Kiefer ◽  
...  

Abstract Emotional stimuli like emotional faces have been frequently shown to be temporally overestimated compared to neutral ones. This effect has been commonly explained by induced arousal caused by emotional processing leading to the acceleration of an inner-clock-like pacemaker. However, there are some studies reporting contradictory effects and others point to relevant moderating variables. Given this controversy, we aimed at investigating the processes underlying the temporal overestimation of emotional faces by combining behavioral and electrophysiological correlates in a temporal bisection task. We assessed duration estimation of angry and neutral faces using anchor durations of 400 ms and 1600 ms while recording event-related potentials. Subjective ratings and the early posterior negativity confirmed encoding and processing of stimuli’s emotionality. However, temporal ratings did not differ between angry and neutral faces. In line with this behavioral result, the Contingent Negative Variation (CNV), an electrophysiological index of temporal accumulation, was not modulated by the faces’ emotionality. Duration estimates, i.e., short or long responses toward stimuli of ambiguous durations of 1000 ms, were nevertheless associated with a differential CNV amplitude. Interestingly, CNV modulation was already observed at 600–700 ms after stimulus onset, i.e., long before stimulus offset. The results are discussed in light of the information-processing model of time perception as well as regarding possible factors of the experimental setup moderating temporal overestimation of emotional stimuli. In sum, combining behavioral and electrophysiological measures seems promising to more clearly understand the complex processes leading to the illusion of temporal lengthening of emotional faces.


2003 ◽  
Vol 15 (7) ◽  
pp. 1039-1051 ◽  
Author(s):  
Ute Leonards ◽  
Julie Palix ◽  
Christoph Michel ◽  
Vicente Ibanez

Functional magnetic resonance imaging studies have indicated that efficient feature search (FS) and inefficient conjunction search (CS) activate partially distinct frontoparietal cortical networks. However, it remains a matter of debate whether the differences in these networks reflect differences in the early processing during FS and CS. In addition, the relationship between the differences in the networks and spatial shifts of attention also remains unknown. We examined these issues by applying a spatio-temporal analysis method to high-resolution visual event-related potentials (ERPs) and investigated how spatio-temporal activation patterns differ for FS and CS tasks. Within the first 450 msec after stimulus onset, scalp potential distributions (ERP maps) revealed 7 different electric field configurations for each search task. Configuration changes occurred simultaneously in the two tasks, suggesting that contributing processes were not significantly delayed in one task compared to the other. Despite this high spatial and temporal correlation, two ERP maps (120–190 and 250–300 msec) differed between the FS and CS. Lateralized distributions were observed only in the ERP map at 250–300 msec for the FS. This distribution corresponds to that previously described as the N2pc component (a negativity in the time range of the N2 complex over posterior electrodes of the hemisphere contralateral to the target hemifield), which has been associated with the focusing of attention onto potential target items in the search display. Thus, our results indicate that the cortical networks involved in feature and conjunction searching partially differ as early as 120 msec after stimulus onset and that the differences between the networks employed during the early stages of FS and CS are not necessarily caused by spatial attention shifts.


Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 147-147
Author(s):  
P Stivalet ◽  
Y Moreno ◽  
C Cian ◽  
J Richard ◽  
P-A Barraud

In a visual search paradigm we measured the stimulus onset asynchrony (SOA) between a stimulus and a mask that was required to reach 90% correct responses. This procedure has the advantage of taking into account the real processing time and excluding the time for the generation of the motor response. Twelve congenitally deaf adult subjects and twelve normal subjects were given a visual search task for a target letter O among a varying number of distractor letters Q and vice-versa. In both groups we found the asymmetrical visual search pattern classically observed with parallel processing for the search for the target Q and with serial processing for the search for the target O (Treisman, 1985 Computer Vision, Graphics, and Image Processing31 156 – 177). The difference between the mean search slopes for an O target was not statistically significant between the groups; this might be due to the variability within the groups. The visual search amidst the congenitally deaf does not seem to benefit from a compensatory effect in relation to the acoustic deprivation. Our results seem to confirm data reported by Neville (1990 Annals of the New York Academy of Science 71 – 91) obtained by an electrophysiological technique based on event-related potentials. Nevertheless, the deaf subjects were 2.5 times faster at the visual search task.


2006 ◽  
Vol 18 (1) ◽  
pp. 1-13 ◽  
Author(s):  
Joel S. Snyder ◽  
Claude Alain ◽  
Terence W. Picton

A general assumption underlying auditory scene analysis is that the initial grouping of acoustic elements is independent of attention. The effects of attention on auditory stream segregation were investigated by recording event-related potentials (ERPs) while participants either attended to sound stimuli and indicated whether they heard one or two streams or watched a muted movie. The stimuli were pure-tone ABA-patterns that repeated for 10.8 sec with a stimulus onset asynchrony between A and B tones of 100 msec in which the A tone was fixed at 500 Hz, the B tone could be 500, 625, 750, or 1000 Hz, and was a silence. In both listening conditions, an enhancement of the auditory-evoked response (P1-N1-P2 and N1c) to the B tone varied with f and correlated with perception of streaming. The ERP from 150 to 250 msec after the beginning of the repeating ABA-patterns became more positive during the course of the trial and was diminished when participants ignored the tones, consistent with behavioral studies indicating that streaming takes several seconds to build up. The N1c enhancement and the buildup over time were larger at right than left temporal electrodes, suggesting a right-hemisphere dominance for stream segregation. Sources in Heschl's gyrus accounted for the ERP modulations related to f-based segregation and buildup. These findings provide evidence for two cortical mechanisms of streaming: automatic segregation of sounds and attention-dependent buildup process that integrates successive tones within streams over several seconds.


2006 ◽  
Vol 18 (9) ◽  
pp. 1488-1497 ◽  
Author(s):  
James W. Tanaka ◽  
Tim Curran ◽  
Albert L. Porterfield ◽  
Daniel Collins

Electrophysiological studies using event-related potentials have demonstrated that face stimuli elicit a greater negative brain potential in right posterior recording sites 170 msec after stimulus onset (N170) relative to nonface stimuli. Results from repetition priming paradigms have shown that repeated exposures of familiar faces elicit a larger negative brainwave (N250r) at inferior temporal sites compared to repetitions of unfamiliar faces. However, less is known about the time course and learning conditions under which the N250 face representation is acquired. In the familiarization phase of the Joe/no Joe task, subjects studied a target “Joe” face (“Jane” for female subjects) and, during the course of the experiment, identified a series of sequentially presented faces as either Joe or not Joe. The critical stimulus conditions included the subject's own face, a same-sex Joe ( Jane) face and a same-sex “other” face. The main finding was that the subject's own face produced a focal negative deflection (N250) in posterior channels relative to nontarget faces. The task-relevant Joe target face was not differentiated from other nontarget faces in the first half of the experiment. However, in the second half, the Joe face produced an N250 response that was similar in magnitude to the own face. These findings suggest that the N250 indexes two types of face memories: a preexperimentally familiar face representation (i.e., the “own face” and a newly acquired face representation (i.e., the Joe/Jane face) that was formed during the course of the experiment.


2017 ◽  
Author(s):  
Daniel Feuerriegel ◽  
Owen Churches ◽  
Scott Coussens ◽  
Hannah A. D. Keage

AbstractRepeated stimulus presentation leads to complex changes in cortical neuron response properties, commonly known as repetition suppression or stimulus-specific adaptation. Circuit-based models of repetition suppression provide a framework for investigating patterns of repetition effects that propagate through cortical hierarchies. To further develop such models it is critical to determine whether (and if so, when) repetition effects are modulated by top-down influences, such as those related to perceptual expectation. We investigated this by presenting pairs of repeated and alternating face images, and orthogonally manipulating expectations regarding the likelihood of stimulus repetition. Event-related potentials (ERPs) were recorded from n=39 healthy adults, to map the spatiotemporal progression of stimulus repetition and expectation effects, and interactions between these factors, using mass univariate analyses. We also tested whether the ability to predict unrepeated (compared to repeated) face identities could influence the magnitude of observed repetition effects, by presenting separate blocks with predictable and unpredictable alternating faces. Multiple repetition and expectation effects were identified between 99-800ms from stimulus onset, which did not statistically interact at any point. Repetition effects in blocks with predictable alternating faces were smaller than in unpredictable alternating face blocks between 117-179ms and 506-652ms, and larger between 246-428ms. ERP repetition effects appear not to be modulated by perceptual expectations, supporting separate mechanisms for repetition and expectation suppression. However, previous studies that aimed to test for repetition effects, in which the repeated (but not unrepeated) stimulus was predictable, are likely to have conflated repetition and stimulus predictability effects.Highlights- ERP face image repetition effects were apparent between 99-800ms from stimulus onset- Expectations of stimulus image properties did not modulate face repetition effects- The predictability of unrepeated stimuli influenced repetition effect magnitudes


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