Negative priming for obsessive-compulsive checkers and noncheckers

Negative priming--the slowing of a response to an item that was recently ignored--was investigated in three groups: obsessive-compulsive disorder (OCD) checkers, OCD noncheckers, and nonclinical control participants. All groups performed both a standard negative priming task, selecting targets based on a perceptual feature (i.e., color), and a modified negative priming task, selecting targets based on a semantic feature (i.e., referent size). All three groups demonstrated significant negative priming in both tasks, although the negative priming was much larger in the novel, semantic task than in the common, perceptual one. The findings suggest that patients with OCD do not demonstrate impairments in negative priming, contrary to earlier claims (Enright & Beech, 1990, 1993a, 1993b; Enright, Beech, & Claridge, 1995).     

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.     

Simply shapely: Relative, not absolute shapes are primed in pop-out search

Visual search is typically faster when the target from the previous trial is repeated than when it changes. This priming effect is commonly attributed to a selection bias for the target feature value or against the nontarget feature value that carries over to the next trial. By contrast, according to a relational account, what is primed in visual search is the target–nontarget relationship—namely, the feature that the target has in relation to the features in the nontarget context (e.g., larger, darker, redder)—and switch costs occur only when the target–nontarget relations reverse across trials. Here, the relational account was tested against current feature-based views in three eye movement experiments that used different shape search tasks (e.g., geometrical figures varying in the number of corners). For all tested shapes, reversing the target–nontarget relationships produced switch costs of the same magnitude as directly switching the target and nontarget features across trials (“full-switch”). In particular, changing only the nontargets produced large switch costs, even when the target feature was always repeated across trials. By contrast, no switch costs were observed when both the target and nontarget features changed, such that the coarse target–nontarget relations remained constant across trials. These results support the relational account over feature-based accounts of priming and indicate that a target’s shape can be encoded relative to the shapes in the nontarget context.     

整体-局部范式下的负启动效应

在通常的负启动范式基础上 ,以小数字构成的大数字 ,即以同时具有整体特征和局部特征的复合数字为实验材料 ,采用数字命名任务 ,将刺激画面中复合数字的数目和注意指向作为变量进行实验。大学生充任被试。结果发现 ,在单个复合数字条件下对同一客体的非注意指向的特征进行忽略重复 ,注意整体时出现负启动 ,而注意局部时不出现负启动 ;在两个复合数字条件下对启动刺激中充当干扰项的复合数字进行忽略重复 ,则注意整体与注意局部都出现了负启动。该研究表明 ,在不同注意指向时 ,整体 -局部范式下的负启动效应具有知觉组织的层次性 ,并显示出客体内选择和客体间选择对负启动的不同影响。     

The mechanism of priming: episodic retrieval or priming of pop-out?

Previous studies indicate that priming affects attentional processes, facilitating processes of target detection and selection on repetition trials. However, the results are so far compatible with two different attentional views that propose entirely different mechanisms to account for priming. The priming of pop-out hypothesis explains priming by feature weighting processes that lead to more frequent selections of nontarget items on switch trials. According to the episodic retrieval account, switch trials conversely lead to temporal delays in retrieving priority rules that specify the target. The results from two eye tracking experiments clearly favour the priming of pop-out hypothesis: Switching the target and nontarget features leads to more frequent selection of nontargets, without affecting the time-course of saccades to a great extent. The results from two more control experiments demonstrate that the same results can be obtained in a visual search task that allows only covert attention shifts. This indicates that eye movements can reliably indicate covert attention shifts in visual search.     

Understanding priming of color-singleton search: Roles of attention at encoding and “retrieval”

We investigated how the performance of a color-singleton search (the search for a single odd-colored item among homogeneously colored distractors) left a persistent memory trace (lasting up to six intervening trials or ～17 sec) that facilitated a subsequent color-singleton search (when the same targetdistractor color combination was repeated). Specifically, we investigated the roles of attention in the encoding and “retrieval” stages of this priming effect by intermixing trials in which the target location was precued by an onset cue. We found that the encoding of both target and distractor colors was automatic in that whether or not observers had to use color in locating the target in the preceding trial did not substantially affect priming. However, priming required that the color-singleton item be attended in the preceding trial. Once a color singleton display was encoded, our results indicated that priming facilitated the direction of attention to the color-singleton target on a subsequent trial. In short, when a color-singleton item happened to be a critical item to be attended in one situation, another color-singleton item defined by the same color combination tended to attract attention in subsequent encounters.     

Understanding priming of color-singleton search: roles of attention at encoding and "retrieval"

We investigated how the performance of a color-singleton search (the search for a single odd-colored item among homogeneously colored distractors) left a persistent memory trace (lasting up to six intervening trials or approximately 17 sec) that facilitated a subsequent color-singleton search (when the same target-distractor color combination was repeated). Specifically, we investigated the roles of attention in the encoding and "retrieval" stages of this priming effect by intermixing trials in which the target location was precued by an onset cue. We found that the encoding of both target and distractor colors was automatic in that whether or not observers had to use color in locating the target in the preceding trial did not substantially affect priming. However, priming required that the color-singleton item be attended in the preceding trial. Once a color singleton display was encoded, our results indicated that priming facilitated the direction of attention to the color-singleton target on a subsequent trial. In short, when a color-singleton item happened to be a critical item to be attended in one situation, another color-singleton item defined by the same color combination tended to attract attention in subsequent encounters.     

Episodic retrieval and feature facilitation in intertrial priming of visual search

Huang, Holcombe, and Pashler (Memory & Cognition, 32, 12-20, 2004) found that priming from repetition of different features of a target in a visual search task resulted in significant response time (RT) reductions when both target brightness and size were repeated. But when only one feature was repeated and the other changed, RTs were longer than when neither feature was repeated. From this, they argued that priming in visual search reflected episodic retrieval of memory traces, rather than facilitation of repeated features. We tested different variations of the search task introduced by Huang et al., with the aim of uncovering when priming is episodic and when feature based. We found that varying the signal strength of target against distractors had a strong effect on the priming pattern. In difficult search with low signal-to-noise ratios of target against distractors, the priming patterns were episodic. When feature contrasts between target and distractors were increased, priming of different features was independent and additive. Our results suggest that, during inefficient search,priming can be episodic but that, for more efficient search, priming from different features occurs independently. The results support two-stage (or multistage) accounts of priming in visual search.     

No evidence for a cue mismatch in negative priming

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.     

Effect of stimulus repetition on positive and negative identity priming

Most negative-priming experiments have used a limited number of stimuli that are repeated many times throughout the experiment. We report five experiments that examine in greater detail the role of stimulus repetition in negative priming. Subjects were presented with displays consisting of two or more words, and were required to name the word printed in red. On attended repetition (AR) trials, the target word was the same as the target word on the preceding trial. On ignored repetition (IR) trials, the target word was the same as the distractor word on the preceding trial. Experiments 1 and 2 used novel words, and obtained positive priming on AR trials, but no negative priming on IR trials. Experiments 3 and 4 used repeated words, and obtained negative priming on IR trials, but no positive priming on AR trials. In Experiment 5, both novel and repeated words were intermixed, and negative priming was observed for repeated, but not novel, IR conditions, whereas positive priming was observed for novel, but not repeated, AR conditions. Together, Experiments 1–5 demonstrate that positive and negative identity priming are modulated by stimulus repetition and are stimulus specific.     

The effects of response stimuli interval on error priming in sequential object naming

Two experiments are reported, which examine the effect of altering response stimulus interval on the positive and negative error priming effects found during sequential object naming. Positive error priming refers to errors that relate to earlier responses at above chance rates. Negative error priming refers to the absence of errors that refer to the immediately preceding trial in particular (Lag 1), and this has been interpreted as a brief inhibitory effect. In Experiment 1, a series of pictures of animals were presented, with either 4 or 8sec intervening between response and next stimulus (RSI). Positive and negative error priming was evident in both conditions, though the positive error priming appeared to be attributable to only a subsection of the participants. Errors began to emerge at shorter lags in the 8sec RSI condition than the 4sec RSI condition, and this is inconsistent with any account which suggests inhibition is released after the next trial. In Experiment 2, the RSIs between related animal pictures were just over 8 and 16sec, and an intervening unrelated item was included between related pictures. Lag 1 errors were now the most frequent response in the long RSI condition, and there was an increase in the incidence of Lag 1 errors across RSI conditions. A preliminary assessment of the effects of adding an unrelated item suggested that it may cause a partial release from inhibition. Taken together, the data are consistent with the theory that inhibition decays over time, and the results are discussed with reference to other inhibitory effects in cognition.     

Dissociable interference-control processes in perception and memory

Control over interference is a pervasive feature of cognitive life. Central to research on interference control has been the identification of its underlying mechanisms. Investigations have focused on processes that filter out distracting perceptual information, leading to negative priming, and processes that discard intruding memories that cause proactive interference. Theories differ regarding whether or not a single process during episodic retrieval underlies both negative priming and the resolution of proactive interference. Using functional magnetic resonance imaging, we combined both phenomena into a single paradigm and found that occipital cortex shows activation uniquely related to negative priming, whereas activation increases in left lateral prefrontal cortex are uniquely associated with proactive interference. This pattern of results contradicts theories that rely on a single process to account for both phenomena. However, results also showed common recruitment of right dorsolateral prefrontal cortex and parietal regions and therefore suggest that some control processes are shared.     

Priming effects under correct change detection and change blindness

In three experiments, we investigated the priming effects induced by an image change on a successive animate/inanimate decision task. We studied both perceptual (Experiments 1 and 2) and conceptual (Experiment 3) priming effects, under correct change detection and change blindness (CB). Under correct change detection, we found larger positive priming effects on congruent trials for probes representing animate entities than for probes representing artifactual objects. Under CB, we found performance impairment relative to a “no-change” baseline condition. This inhibition effect induced by CB was modulated by the semantic congruency between the changed item and the probe in the case of probe images, but not for probe words. We discuss our results in the context of the literature on the negative priming effect.     

An Item specific Locus of Repetition Priming

Two principal types of account of repetition priming postulate either facilitation of activation of perceptual representations used in stimulus recognition, or retrieval of specific processing episodes as possible mechanisms by which the effect occurs; these make different predictions concerning the priming of two stimuli presented simultaneously. In Experiments 1-3, subjects made same/different decisions about picture-word stimulus pairs. Recombining the pairings of a subset of items between training and test encounters did not significantly reduce the benefit in response time from repetition, as compared to pairs repeated intact. Subjects were able to remember the pairings (Experiment 4), but this did not influence repetition priming. Instead, the memory representations underlying the priming of each item in a pair were independent. No priming was found between pictures seen at training and words at test, and vice versa (Experiment 5), indicating that representations underlying the repetition effect were domain-specific. In Experiment 6, stimuli were all from within the domain of object pictures. Again, recombining the pairings of items between training and test did not significantly reduce the benefit in response time from repetition, as compared to pairs repeated intact. These results reveal an item-specific locus for repetition priming, consistent with priming occurring within pre-semantic perceptual representation systems involved in item recognition. The findings pose problems for theories that argue that repetition effects result only from retrieval of entire processing episodes.     

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.     

An attention account of neural priming

Repetition priming of familiar stimuli (e.g., objects) produces a decrease in visual cortical activity for repeated versus novel items, which has been attributed to more fluent processing for repeated items. By contrast, priming of unfamiliar stimuli (e.g., abstract shapes) produces an increase in visual cortical activity. The mechanism for priming-related increases in activity for repeated unfamiliar stimuli is unknown. We hypothesised that such increases in activity may reflect attentional allocation to these items. We tested this hypothesis using a priming-spatial attention paradigm. During Phase 1 of Experiment 1, participants viewed unfamiliar abstract shapes and familiar objects. During Phase 2, participants identified target letters (S or H). Each target letter was preceded by a non-informative shape or object cue that was repeated (from Phase 1) or novel in the same (valid) or opposite (invalid) hemifield. In Experiment 2, we manipulated shape familiarity by presenting shapes once or six times during Phase 1. For both experiments, at valid locations, target identification accuracy was higher following repeated versus novel unfamiliar item cues and lower following repeated versus novel familiar item cues. These findings support our hypothesis that priming-related increases in visual cortical activity for repeated unfamiliar items may, in part, reflect attentional allocation.     

Negative priming without ignoring

Negative priming is conventionally defined by slowed responses to a target item that appeared previously as a distractor. As a result, it is widely assumed that negative priming is caused by an act of ignoring. Three experiments are reported in which novel abstract shapes were studied with either “shallow” or “deep” encoding instructions. This study phase was followed by asame-different discrimination task similar to that employed by DeSchepper and Treisman (1996). Same-different discrimination was slower for old than for new target shapes, and this negative priming effect depended on the difficulty of the discrimination task. The results suggest that negative priming may not be caused by the ignoring of a prime stimulus.     

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.     

Predicting semantic priming at the item level

The current study explores a set of variables that have the potential to predict semantic priming effects for 300 prime-target associates at the item level. Young and older adults performed either lexical decision (LDT) or naming tasks. A multiple regression procedure was used to predict priming based upon prime characteristics, target characteristics, and prime-target semantic similarity. Results indicate that semantic priming (a) can be reliably predicted at an item level; (b) is equivalent in magnitude across standardized measures of priming in LDTs and naming tasks; (c) is greater following quickly recognized primes; (d) is greater in LDTs for targets that produce slow lexical decision latencies; (e) is greater for pairs high in forward associative strength across tasks and across stimulus onset asynchronies (SOAs); (f) is greater for pairs high in backward associative strength in both tasks, but only at a long SOA; and (g) does not vary as a function of estimates from latent semantic analysis (LSA). Based upon these results, it is suggested that researchers take extreme caution in comparing priming effects across different item sets. Moreover, the current findings lend support to spreading activation and feature overlap theories of priming, but do not support priming based upon contextual similarity as captured by LSA.     

Predicting semantic priming at the item level

The current study explores a set of variables that have the potential to predict semantic priming effects for 300 prime–target associates at the item level. Young and older adults performed either lexical decision (LDT) or naming tasks. A multiple regression procedure was used to predict priming based upon prime characteristics, target characteristics, and prime–target semantic similarity. Results indicate that semantic priming (a) can be reliably predicted at an item level; (b) is equivalent in magnitude across standardized measures of priming in LDTs and naming tasks; (c) is greater following quickly recognized primes; (d) is greater in LDTs for targets that produce slow lexical decision latencies; (e) is greater for pairs high in forward associative strength across tasks and across stimulus onset asynchronies (SOAs); (f) is greater for pairs high in backward associative strength in both tasks, but only at a long SOA; and (g) does not vary as a function of estimates from latent semantic analysis (LSA). Based upon these results, it is suggested that researchers take extreme caution in comparing priming effects across different item sets. Moreover, the current findings lend support to spreading activation and feature overlap theories of priming, but do not support priming based upon contextual similarity as captured by LSA.