The Time-Course of Masked Negative Priming

2009 ◽  
Vol 56 (5) ◽  
pp. 301-306 ◽  
Author(s):  
Christian Frings ◽  
Andreas B. Eder
Keyword(s):  
Negative Priming ◽  
Time Course ◽  
Temporal Discrimination ◽  
Reaction Times ◽  
Simultaneous Presentation ◽  
Probe Display ◽  
Decay Function ◽  
Rapid Decay ◽  
Prime Display ◽  
Prime Distractor

Negative priming (NP) refers to the finding that reaction times and errors increase when a previously ignored prime distractor is presented as a target. In a variant of this task, the prime display is composed of only a single masked distractor that is followed by the simultaneous presentation of a target and a distractor in the probe display. In one experiment, we explore the time-course of masked NP using different variations of the prime-probe interval (short, medium, and long), and compare the results with time-course investigations of unmasked NP. We found clear evidence for a rapid-decay function of masked NP: With an increase in the prime-probe interval, masked NP decreased. This result is in line with the predictions of the temporal discrimination account and retrieval accounts of NP.

Identity-Based Crossmodal Negative Priming: Aftereffects of Ignoring in One Sensory Modality on Responding to Another Sensory Modality

2020 ◽  
Vol 33 (7) ◽  
pp. 703-721
Author(s):  
Ann-Katrin Wesslein ◽  
Christian Frings
Keyword(s):  
Negative Priming ◽  
Sensory Modality ◽  
Probe Display ◽  
Distractor Stimulus ◽  
Probe Sequence ◽  
Probe Target ◽  
Prime Display ◽  
Identity Based ◽  
Display Control ◽  
Prime Distractor

Abstract Negative Priming (NP) refers to the phenomenon that responses towards previously ignored stimuli, as compared to new stimuli, are impaired. That is, NP is reflected in the performance on the probe display of a prime–probe sequence. NP is established in vision, audition and touch. In the current study, we presented participants with auditory, visual, and tactile manifestations of the same temporal patterns in order to measure NP across the senses. On each trial, the sensory modality shifted from the prime to the probe. Each prime and probe display consisted of a target and a distractor stimulus, presented to the same sensory modality. On some trials, the prime distractor repeated as probe target (ignored-repetition trials), on other trials the probe stimuli had not been involved in the prime display (control trials). We observed NP between audition and touch (Experiment 1) and between vision and audition (Experiment 2). These findings indicate that the processes underpinning NP can operate at an amodal, postperceptual level.

Short article: No evidence for a cue mismatch in negative priming

2009 ◽  
Vol 62 (4) ◽  
pp. 645-652 ◽  
Author(s):  
Susanne Mayr ◽  
Robert Hauke ◽  
Axel Buchner ◽  
Michael Niedeggen
Keyword(s):  
Negative Priming ◽  
Visual Discrimination ◽  
Negative Priming Effect ◽  
Episodic Retrieval ◽  
Short Article ◽  
Prime Display ◽  
Novel Variant ◽  
Prime Distractor ◽  
Mismatch Condition ◽  
Mismatch Hypothesis

An experiment is reported in which the cue mismatch hypothesis of negative priming, an important novel variant of the mismatching hypothesis, was tested. A cue mismatch and a no mismatch condition were contrasted in a visual discrimination task. In the prime display of cue mismatch ignored-repetition trials, the colour of the prime distractor was different from the colour of the cue indicating the selection feature (coloured square). In probe displays, cue and repeated stimulus had the same colour. In the no mismatch condition, the visual cue was neutral in terms of colour (always black), so that there was always no cue mismatch between prime and probe displays. Contrary to the prediction of the cue mismatch hypothesis, the negative priming effect was not larger in the cue mismatch than in the no mismatch condition. The cue mismatch hypothesis must therefore be rejected. In contrast, the episodic retrieval account is consistent with the results.

The Negative Priming Effect: Inhibitory Priming by Ignored Objects

1985 ◽  
Vol 37 (4) ◽  
pp. 571-590 ◽  
Author(s):  
Steven P. Tipper
Keyword(s):  
Negative Priming ◽  
Priming Effect ◽  
Internal Representation ◽  
Negative Priming Effect ◽  
Probe Display ◽  
Stimulus Interval ◽  
Prime Display ◽  
Priming Paradigm ◽  
Naming Latencies ◽  
Selection Of

A priming paradigm was employed to investigate the processing of an ignored object during selection of an attended object. Two issues were investigated: the level of internal representation achieved for the ignored object, and the subsequent fate of this representation. In Experiment 1 a prime display containing two superimposed objects was briefly presented. One second later a probe display was presented containing an object to be named. If the ignored object in the prime display was the same as the subsequent probe, naming latencies were impaired. This effect is termed negative priming. It suggests that internal representations of the ignored object may become associated with inhibition during selection. Thus, selection of a subsequent probe object requiring these inhibited representations is delayed. Experiment 2 replicated the negative priming effect with a shorter inter-stimulus interval. Experiment 3 examined the priming effects of both the ignored and the selected objects. The effect of both identity repetition and a categorical relationship between prime and probe stimuli were investigated. The data showed that for a stimulus selected from the prime display, naming of the same object in the probe display was facilitated. When the same stimulus was ignored in the prime display, however, naming of it in the probe display was again impaired (negative priming). That negative priming was also demonstrated with categorically related objects suggests that ignored objects achieve categorical levels of representation, and that the inhibition may be at this level.

The Level of Reaction Time Determines the ERP Correlates of Auditory Negative Priming

2006 ◽  
Vol 20 (3) ◽  
pp. 186-194 ◽  
Author(s):  
Susanne Mayr ◽  
Michael Niedeggen ◽  
Axel Buchner ◽  
Guido Orgs
Keyword(s):  
Reaction Time ◽  
Negative Priming ◽  
Effect Size ◽  
Priming Effect ◽  
Reaction Times ◽  
Negative Priming Effect ◽  
Episodic Retrieval ◽  
Time Level ◽  
Fast Reactions ◽  
Priming Condition

Responding to a stimulus that had to be ignored previously is usually slowed-down (negative priming effect). This study investigates the reaction time and ERP effects of the negative priming phenomenon in the auditory domain. Thirty participants had to categorize sounds as musical instruments or animal voices. Reaction times were slowed-down in the negative priming condition relative to two control conditions. This effect was stronger for slow reactions (above intraindividual median) than for fast reactions (below intraindividual median). ERP analysis revealed a parietally located negativity of the negative priming condition compared to the control conditions between 550-730 ms poststimulus. This replicates the findings of Mayr, Niedeggen, Buchner, and Pietrowsky (2003) . The ERP correlate was more pronounced for slow trials (above intraindividual median) than for fast trials (below intraindividual median). The dependency of the negative priming effect size on the reaction time level found in the reaction time analysis as well as in the ERP analysis is consistent with both the inhibition as well as the episodic retrieval account of negative priming. A methodological artifact explanation of this effect-size dependency is discussed and discarded.

Reversed Memory Coding and Symbol Reversal in Children

1983 ◽  
Vol 56 (2) ◽  
pp. 431-437
Author(s):  
James F. Curley ◽  
Maureen A. Hogan
Keyword(s):  
Reaction Times ◽  
Simultaneous Presentation ◽  
Normal Group ◽  
Cerebral Hemispheres ◽  
Perceptual Task ◽  
Experimental Task ◽  
Bilateral Presentation

The present study examined an hypothesized mirror-reversed memory-coding phenomenon whereby aligned and mirror-reversed memory records in opposite cerebral hemispheres are confused. Two groups of 7-yr.-old boys were chosen on the basis of tendency to confuse mirror and aligned written symbols. The experimental task required discrimination as same or different of letter pairs which were either same or different and either aligned or mirror-reversed. The pairs were simultaneously presented to right, left, or both cerebral hemispheres. The reversing group had slower reaction times than the normal group in all conditions. Evidence was insufficient to conclude that mirror-same bilateral presentation facilitated responses of either group over aligned-same or peripheral conditions. This result would have been necessary to indicate the presence of a mirror-reversed code across the hemispheres. Research utilizing delayed as well as simultaneous presentation of stimuli to children of various ages would clarify this ambiguity. Bilateral processing across conditions proved easier for both groups, indicating adequate hemispheric integration on a visual-perceptual task even in children who tended to confuse mirror images.

Binding of Event Files in a (go/no-go) Simon Task With an Accessory Peripheral Signal

2009 ◽  
Vol 56 (2) ◽  
pp. 100-111 ◽  
Author(s):  
Kathleen Maetens ◽  
David Henderickx ◽  
Eric Soetens
Keyword(s):  
Simon Effect ◽  
Time Course ◽  
Simon Task ◽  
Reaction Times ◽  
Response Signal ◽  
Event File ◽  
Response Information ◽  
Event Files ◽  
Accessory Stimulus ◽  
Accessory Signal

To understand the relation between the Simon effect and the time course of relevant and irrelevant code activations, we presented the response signal before or simultaneously with a go/no-go signal in an accessory Simon task. A peripheral accessory signal could appear before, simultaneously with or after the go/no-go signal. We observed a Simon effect when the accessory signal was presented just before or simultaneously with the go signal, irrespective of the delay between response and go/no-go signal. The Simon effect reversed when the accessory signal was presented 150 ms after the go signal when response information was presented first and the participants had to make a go/no-go decision afterwards or when they had to select a response when the go signal appeared. The reversal did not occur when both decisions were required at the same time. Our data suggest that the integration and release of event files are involved in the occurrence of the reversal. Response activation induced by the accessory stimulus facilitates/interferes with the response when it is presented before the event file is integrated. When the accessory stimulus is presented after integration, the automatically activated response is inhibited, causing a delay in the corresponding reaction times.

The Time Course of Perceptual Grouping in Natural Scenes

2012 ◽  
Vol 23 (12) ◽  
pp. 1482-1489 ◽  
Author(s):  
Ilia Korjoukov ◽  
Danique Jeurissen ◽  
Niels A. Kloosterman ◽  
Josine E. Verhoeven ◽  
H. Steven Scholte ◽  
...  
Keyword(s):  
Visual Perception ◽  
Perceptual Grouping ◽  
Time Course ◽  
Reaction Times ◽  
Object Classification ◽  
Natural Scenes ◽  
Single Object ◽  
Object A ◽  
Object Parsing ◽  
Different Parts

Visual perception starts with localized filters that subdivide the image into fragments that undergo separate analyses. The visual system has to reconstruct objects by grouping image fragments that belong to the same object. A widely held view is that perceptual grouping occurs in parallel across the visual scene and without attention. To test this idea, we measured the speed of grouping in pictures of animals and vehicles. In a classification task, these pictures were categorized efficiently. In an image-parsing task, participants reported whether two cues fell on the same or different objects, and we measured reaction times. Despite the participants’ fast object classification, perceptual grouping required more time if the distance between cues was larger, and we observed an additional delay when the cues fell on different parts of a single object. Parsing was also slower for inverted than for upright objects. These results imply that perception starts with rapid object classification and that rapid classification is followed by a serial perceptual grouping phase, which is more efficient for objects in a familiar orientation than for objects in an unfamiliar orientation.

Radical scavenging characteristics of condensed tannins from barks of various tree species compared with quebracho wood tannin

Holzforschung ◽  
2011 ◽  
Vol 65 (5) ◽  
Author(s):  
Rei Makino ◽  
Seiji Ohara ◽  
Koh Hashida
Keyword(s):  
Tree Species ◽  
Time Course ◽  
Condensed Tannin ◽  
Radical Scavenging ◽  
Reaction Times ◽  
Gas Chromatography Mass Spectrometry ◽  
Type B ◽  
Pyrolysis Gas ◽  
Nmr Spectrometry ◽  
In The Beginning

Abstract The object of this study was to elucidate the relationship between the chemical structure of purified condensed tannin polymers from tree species and their radical scavenging characteristics. By means of 13C-NMR spectrometry and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS), four kinds of proanthocyanidins were identified: prorobinetinidins, profisetinidins, procyanidins, and prodelphinidins. The tannins were submitted to radical scavenging assays with DPPH and galvinoxyl radicals and from the time-course of the reactions was concluded: 1) Tannins with pyrogallol type B-ring scavenge radicals in the beginning faster than those with catechol type B-ring. 2) Tannins with catechol type B-ring needs more time to scavenge the same amount of radicals as those with pyrogallol type B-ring. 3) The IC50 values of tannins with catechol type B-ring decrease after longer reaction times with the galvinoxyl radical. 4) Radical scavenging with DPPH radical proceeds faster than that for the galvinoxyl radical.

Time Course Analysis of the Reverse-Stroop Effect in Japanese Kanji

1998 ◽  
Vol 87 (1) ◽  
pp. 163-174 ◽  
Author(s):  
Kayu Moriguchi ◽  
Yasuo Morikawa
Keyword(s):  
Stroop Effect ◽  
Time Course ◽  
Reaction Times ◽  
Reading Process ◽  
Relative Speed ◽  
Speed Of Processing ◽  
The Difference ◽  
Japanese Kana

A reverse of the Stroop effect was obtained with Japanese kanji (logographic script) but not with Japanese kana (syllabic scripts) by Morikawa in 1981. In the present study, the normal effect on reaction times by word and color was altered by presenting the words before or after the color. The reverse Stroop effect was observed with kanji but not with kana even when the color was presented prior to the word. It was shown that the difference between kanji and kana in the reverse-Stroop effect could not be explained by the relative speed of processing of word and color and that the reading process of kanji is different from that of kana.

The Time Course of Preparation*

1967 ◽  
Vol 19 (3) ◽  
pp. 272-279 ◽  
Author(s):  
Paul Bertelson
Keyword(s):  
Visual Stimulus ◽  
Refractory Period ◽  
Time Course ◽  
Reaction Times ◽  
Warning Signal ◽  
High Time ◽  
Refractory Periods ◽  
Time Uncertainty ◽  
Order Of Magnitude ◽  
Choice Reaction Times

The time course of the adjustments triggered by a warning signal was studied by measuring choice reaction times (RTs) at different predictable foreperiods after such a signal. Before the warning signal, a high time uncertainty situation was created by imposing either a long constant foreperiod of 5 sec. or one varying in the range 1.5 to 5 sec. The warning signal was a click. Foreperiods ranging from 0 to 300 millisec. were used in different blocks of trials. The stimulus was the onset of one of two lamps calling for the pressing of one of two keys. A control condition, without click, was used also. RTs were found to decrease continuously when the forperiod was increased from 0 to 100-150 millisec. The click delivered simultaneously with the stimulus permitted reactions significantly faster than in the control condition. It is concluded (a) that the latency of preparation can be much shorter than the 2 to 4 sec. reported by Woodrow; (b) that the warning signal can be used as a time cue to start preparatory adjustments without starting a refractory period of the order of magnitude found in experiments with pairs of successive reactions, and thus that such refractory periods are not the inevitable cost of paying attention to a signal. There is also some suggestion that in this situation the click not only triggers preparatory adjustments, but also causes an immediate facilitation of the reaction to the visual stimulus.

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