Locus of single-prime negative priming: The role of perceptual form

Single-prime negative priming refers to the phenomenon in which after a single prime word is briefly presented, repeating it as the probe target results in a delay in responding to the target. The present study investigated the locus of this negative priming effect. Experiment 1 showed that repeating the identity of the prime produced a negative priming effect but merely repeating the response of the prime did not. Experiment 2 showed that the negative priming effect transformed into positive priming when the probe distractor was absent. Experiments 3 and 4 further revealed that single-prime negative priming was observed when the perceptual form was repeated. Taken together, these results suggest that single-prime negative priming involves a perceptual locus.     

Effects of perceptual grouping on positive and negative priming

The effects of perceptual grouping/segregation of targets and distractors by means of colour on positive and negative priming were examined in two experiments. In Experiments 1 and 2 we examined whether grouping of target and distractors by means of common colour in the prime display affected positive and negative priming, or whether these effects depend on prime–probe contextual similarity in colour. In addition, we examined the effects of the predictability of target colour in the prime and the probe displays across the experiments using mixed (Experiment 1) or blocked procedures (Experiment 2). The pattern of results was similar in both experiments, indicating that the positive priming effect was determined by target repetition and enhanced by perceptual segregation of target from distractors in the prime display. The negative priming effect was determined by grouping the target and distractors by common colour in the prime display. The results of the present experiments are consistent with inhibition-based models of negative priming.     

Negative priming and perceptual fluency: More than what meets the eye

In two priming experiments, we manipulated the perceptual quality of the target or the distractor on the prime trial; the stimuli were repeated or novel. Negative priming was found to be contingent on stimulus repetition, because it was obtained with repeated items but not with novel items. Prime trial perceptual degradation modulated negative priming for repeated items but had no effect on priming in ignored repetition conditions using novel stimuli. These patterns were obtained even when the effect of perceptual degradation was (1) greater than the effect of stimulus repetition and (2) greater for novel words than for repeated words. Although stimulus repetition increases perceptual fluency, the activation of perceptual representations by itself is not sufficient to produce negative priming. Instead, we suggest that negative priming is a manifestation of an activation-sensitive inhibitory mechanism that functions to reduce response competition.     

Negative priming and perceptual fluency: more than what meets the eye

In two priming experiments, we manipulated the perceptual quality of the target or the distractor on the prime trial; the stimuli were repeated or novel. Negative priming was found to be contingent on stimulus repetition, because it was obtained with repeated items but not with novel items. Prime trial perceptual degradation modulated negative priming for repeated items but had no effect on priming in ignored repetition conditions using novel stimuli. These patterns were obtained even when the effect of perceptual degradation was (1) greater than the effect of stimulus repetition and (2) greater for novel words than for repeated words. Although stimulus repetition increases perceptual fluency, the activation of perceptual representations by itself is not sufficient to produce negative priming. Instead, we suggest that negative priming is a manifestation of an activation-sensitive inhibitory mechanism that functions to reduce response competition.     

The crucial roles of stimulus matching and stimulus identity in negative priming

Negative priming refers to the situation in which an ignored item on an initial prime trial suffers slowed responding when it becomes the target item on a subsequent probe trial. In this experiment (and a replication), we demonstrate two ways in which stimulus consistency (matching) governs negative priming. First, negative priming for identical words occurred only when the prime distractor changed color when it became the probe target (i.e., constant cue to read the red word); negative priming disappeared when the prime distractor retained its color as the probe target (i.e., cue switches from read the red prime word to read the white probe word). Second, negative priming occurred for identical words, but not for semantically related words, whether related categorically or associatively. This pattern of results is consistent with a memory retrieval account, but not with an inhibition account of negative priming, and casts doubt on whether there is semantic negative priming for words.     

Negative priming is not task bound: A consistent pattern across naming and categorization tasks

When a word that was a to-be-ignored flanker on an initial prime trial becomes the target on the subsequent probe trial, responding to that word on the probe trial is slowed, a phenomenon callednegative priming. Virtually all prior studies have required subjects to perform the same task on both the prime and the probe trials. Thus, the extent to which negative priming is task bound is uncertain. We manipulated task factorially on the prime and probe trials, resulting in four groups: name-name, name-categorize, categorize-name, and categorize-categorize. The results showed equivalent negative priming of about 22 msec both within and between tasks for identical words, but no negative priming for semantically related words from the same category. These findings suggest (1) that negative priming for identical words can readily cross task types; and (2) that semantic negative priming does not occur for words, at least when categorical relatedness alone determines the semantic relation.     

Influence of probe-trial selection on the location negative priming effect.

Using the location variant of the typical negative priming procedure, participants were cued (100% reliable) before (Experiment 1) or after (Experiment 2) the prime trial as to whether a distractor would or would not accompany the target on the probe trial. The crucial results were that on cued trials, the predictable absence, produced the removal of the negative priming effect (disengagement), and that this disengagement of the priming process, motivated by the predictable absence of a probe-trial distractor, could take place on-line. These findings demonstrated the "selection-state" dependency (probe trial) of the location negative priming process, supporting inhibition-based and episodic retrieval models in their contention that the ultimate function of this process is to enhance the efficiency of future distractor processing, and hence selection. The disengagement results revealed an adaptive feature of a process that can be detrimental or irrelevant to upcoming processing.     

Single‐prime negative priming in the shape‐matching task: Implications for the role of perceptual segmentation processes

Using the shape‐matching task developed by DeSchepper and Triesman (1996), Loula, Kourtzi, and Shiffrar (2000) demonstrated that negative priming only occurred in that task when minimal segmentation cues were available in the prime display. Loula et al. (2000) interpreted their results as revealing that negative priming in the shape‐matching task is directly caused by difficulty in segmenting the prime target from the prime distractor. We offer an alternative interpretation of their results, suggesting that a failure to observe negative priming when segmentation cues are present was incidental to the perceptual segmentation process. Instead, we provide evidence suggesting that an easier perceptual segmentation task contributes positive priming influences that makes a negative priming effect more difficult to observe. Once these positive priming influences are removed, we observed negative priming both when the perceptual segmentation task is trivial and when perceptual segmentation is not a component of the prime task at all.     

Dissociations between identity and location negative priming

Negative priming refers to the phenomenon of a slowed response time to a previously ignored distractor. Identity negative priming can be observed when the identity of a previous distractor is repeated as the target identity, and location negative priming can be observed when the spatial location of a previous distractor is repeated as the target location. This article reviewed and integrated previous findings and provided empirical evidence to show the dissociations between location and identity negative priming: (a) the removal of probe distractor impeded identity negative priming but not location negative priming; (b) identity negative priming was modulated by the distance between the target and distractor, while location negative priming was not; and (c) perceptual grouping of the target and distractor affected identity negative priming but not location negative priming.     

More than meets the eye: Context effects in word identification

The influence of semantic context on word identification was examined using masked target displays. Related prime words enhanced a signal detection measure of sensitivity in making lexical decisions and in determining whether a probe word matched the target word. When line drawings were used as primes, a similar benefit was obtained with the probe task. Although these results suggest that contextual information affects perceptual encoding, this conclusion is questioned on the grounds that sensitivity in these tasks may be determined by independent contributions of perceptual and contextual information. The plausibility of this view is supported by a simulation of the experiments using a connectionist model in which perceptual and semantic information make independent contributions to word identification. The model also predicts results with two other analytic methods that have been used to argue for priming effects on perceptual encoding.     

The role of probe trial distractors in the production/removal of the spatial negative priming effect

When a current (probe trial) target arises at a location formerly occupied by a distractor event (prime trial; ignored-repetition trial), its reaction time is slower than when it occurs at a previously empty location (control trial), revealing a spatial negative priming (SNP) effect. Here, we examined the influence of prime- and probe trial distractor identity similarity on the retrieval of the stored representations of prime trial processing (i.e., indexed by SNP production), in a context where the prevention of the SNP phenomenon had been motivated (via low probability of probe distractor presence—.25). Two results were important. One, the SNP effect was evident when the prime–probe distractor identities fully matched, but not when they partially or totally mismatched, showing a retrieval role for the probe distractor. Two, target-repeat trial latency facilitation showed the same pattern, indicating that representations of prime target and distractor processing are retrieved together, indicative of an episodic storage format. Since target identity remained fixed, the role of a matching probe distractor identity in SNP production was to presumably complete the triggering requirement (i.e., full event identity matching) for accessing the episodically stored representations.     

Context-specific control and the Stroop negative priming effect

The present study highlights the utility of context-specific learning for different probe types in accounting for the commonly observed dependence of negative priming on probe selection. Using a Stroop priming procedure, Experiments 1a and 1b offered a demonstration that Stroop priming effects can differ qualitatively for selection and no-selection probes when probe selection is manipulated between subjects, but not when it is manipulated randomly from trial to trial within subject (see also Moore, 1994). In Experiments 2 and 3, selection and no-selection probes served as two contexts that varied randomly from trial to trial, but for which proportion repeated was manipulated separately. A context-specific proportion repeated effect was observed in Experiment 2, characterized by modest quantitative shifts in the repetition effects as a function of the context-specific proportion repeated manipulation. However, with a longer intertrial interval in Experiment 3, a context-specific proportion repeated manipulation that focused on the no-selection probes changed the repetition effect qualitatively, from negative priming when the proportion repeated was .25 to positive priming when the proportion repeated was .75. The results are discussed with reference to the role of rapid, context-specific learning processes in the integration of prior experiences with current perception and action.     

情绪评价任务中抑郁个体的分心抑制机制实验研究

本实验使用情绪负启动技术,在情绪评价任务中考察了抑郁个体和正常被试对正、负情绪词分心抑制方面的差异。结果显示,与控制条件下相比,非抑郁控制组被试在负启动条件下对探测显示中正、负性靶子词的反应时间更长;抑郁个体只表现在对探测显示中正性靶子词反应时的延长,负性靶子词未出现负启动效应。结果说明,抑郁个体对负性信息存在抑制机制障碍,对负性信息的偏向与选择性注意中的维持成分有关。这提示心理治疗家应该注重训练抑郁个体对负性信息的抑制能力,预防抑郁复发的目标应集中在注意持续的控制上。     

Revisiting the prime–probe contextual similarity effect on negative priming: The impact of cue variability

In previous studies on negative priming, the effect of prime–probe contextual similarity was not stable. On occasions, negative priming was greater when similar rather than different contexts were presented in a prime and a probe trial; however, at other times, negative priming was not affected by such manipulation. The current study demonstrates that the effect of contextual similarity can be optimised when cue variability is high. Cue variability was manipulated between-subject across Experiments 1a and 1b and as a within-subject variable in Experiment 2. Symbols were presented as contextual cues. The results indicated that when cue variability was high, the prime–probe contextual similarity effect was observed on negative priming; however, when cue variability was low, the contextual similarity effect and the negative priming effect were absent.     

PRP-paradigm provides evidence for a perceptual origin of the negative compatibility effect

Visual stimuli (primes) that are made invisible by masking can affect motor responses to a subsequent target stimulus. When a prime is followed by a mask which is followed by a target stimulus, an inverse priming effect (or negative compatibility effect) has been found: Responses are slow and frequently incorrect when prime and target stimuli are congruent, but fast and accurate when prime and target stimuli are incongruent. To functionally localize the origins of inverse priming effects, we applied the psychological refractory period (PRP-) paradigm which distinguishes a perceptual level, a central bottleneck, and a level of motor execution. Two dual-task experiments were run with the PRP-paradigm to localize the inverse priming effect relative to the central bottleneck. Together, results of the Effect-Absorption and the Effect-Propagation Procedure suggest that inverse priming effects are generated by perceptual mechanisms. We suggest two perceptual mechanisms as the source of inverse priming effects.     

Taking a bright view of negative priming in the light of dim stimuli: further evidence for memory confusion during episodic retrieval.

A same-different letter-matching task was used to examine the effects of stimulus intensity on negative priming, which is poorer performance when target letters have been presented as distractor letters on the immediately preceding trial. In Experiment 1, stimulus intensity was manipulated between-participants, whereas in Experiment 2, it varied randomly from trial-to-trial within-participants. In Experiment 1, negative priming was equivalent for both stimulus intensities. In Experiment 2, negative priming effects were larger for repeated intensity stimuli than for nonrepeated intensity stimuli, when stimulus intensity was dim. Furthermore, for repeated intensity stimuli, negative priming effects were enhanced when the overt response required to the stimulus was repeated from prime to probe trial. These results are consistent with the hypothesis that negative priming may be due to memory confusion, rather than to inhibition of the distractor stimuli.     

ERP correlates of auditory negative priming

Negative priming refers to slowed down reactions when the distractor on one trial becomes the target on the next. Following two popular accounts, the effect might be due either to inhibitory processes associated with the frontal cortex, or to an ambiguity in the retrieval of episodic information. We used event-related brain potentials (ERPs) to identify the processing stage primarily associated with negative priming. In an auditory categorization task, reactions in negative priming trials were compared to reactions in a standard control (unrelated primes and probes) and a repetition control (attended prime=ignored probe) condition. Reactions were slower for negative priming than for standard control (Delta32 ms) and repetition control trials (Delta64 ms). The corresponding ERP effect was reflected in an attenuation of a sustained parietal positivity extending from 300 to 600 ms. Because corresponding ERP components were found to be sensitive to stimulus recognition and familiarity, the results may be interpreted to support an episodic retrieval account of negative priming.     

The perceptual wink model of non-switching attentional blink tasks

The attentional blink (AB) is a temporary deficit for a second target (T2) when that target appears after a first target (T1). Although sophisticated models have been developed to explain the substantial AB literature in isolation, the current study considers how the AB relates to perceptual dynamics more broadly. We show that the time-course of the AB is closely related to the time course of the transition from positive to negative repetition priming effects in perceptual identification. Many AB tasks involve a switch between a T1 defined in one manner and a T2 defined in a different manner. Other AB tasks are non-switching, with all targets belonging to the same well-known category (e.g., letter targets versus number distractors) or sharing the same perceptual feature. We propose that these non-switching AB tasks reflect perceptual habituation for the target-defining attribute; thus, a ‘perceptual wink’, with perception of one attribute (target identity) undisturbed while perception of another (target detection) is impaired. On this account, the immediate benefit following T1 (lag-1 sparing) reflects positive repetition priming and the subsequent deficit (the blink) reflects negative repetition priming for the realization that a target occurred. In developing the perceptual wink model, we extended the nROUSE model of perceptual priming to explain the results of two new experiments combining the AB and identity repetitions. This establishes important connections between non-switching AB tasks and perceptual dynamics.     

Negative priming without probe selection

Responses to an object may be slower or less accurate if that object shares attributes with a recently ignored object(negative priming). Some studies have found negative priming only if the probe trial required selection against a distractor stimulus. In the present experiment, subjects responded to the location of a target (O), ignoring a distractor (X) if it appeared in another location. Reaction time was slower to probe targets that appeared in the same location as the prime distractor, regardless of whether or not the probe target was accompanied by a distractor.     

Independent priming of location and color in identification of briefly presented letters

Attention shifts are facilitated if the items to be attended remain the same across trials. Some researchers argue that this priming effect is perceptual, whereas others propose that priming is postperceptual, involving facilitated response selection. The experimental findings have not been consistent regarding the roles of variables such as task difficulty, response repetition, expectancies, and decision-making. Position priming, when repetition of a target position facilitates responses on a subsequent trial, is another source of disagreement among researchers. Experimental results have likewise been inconsistent as to whether position priming is dependent on the repetition of target features or has an independent effect on attention shifts. We attempted to isolate the perceptual components of priming by presenting brief (10–180 ms) search arrays to eight healthy observers. The task was to identify a color-singleton letter among distractors. All stimulus presentation contingencies were randomized, and responses were unspeeded, to avoid effects of observer expectation and postperceptual effects. Repeating target color and/or position strongly improved performance. The effects of color and position repetition were independent of one another and were stable across participants. The results argue for a strong perceptual component in priming, which biases selection toward recent target features and positions, showing that perceptual mechanisms are sufficient to produce priming in visual search and that such effects can be elicited with limited sensory evidence. The results are the first to demonstrate independent priming of color and position in the identification of briefly presented, postmasked stimuli.