Negative priming and multiple repetition: A reply to Grison and Strayer (2001)

Strayer and colleagues (Grison & Strayer, 2001; Malley & Strayer, 1995; Strayer & Grison, 1999) have reported experiments in which negative priming by ignored stimuli occurred only for stimuli that were repeatedly sampled from small sets. These results were argued to be inconsistent with episodic/mismatch accounts of negative priming. We show here that a dependence of negative priming on multiple repetition is wholly consistent with such theories. Furthermore, we argue that the inhibitory theory proposed by Strayer and colleagues cannot account for major findings regarding negative priming and that anomalies in the data reported by Grison and Strayer are more parsimoniously explained by episodic/mismatch accounts.     

Negative priming and stimulus familiarity: What causes opposite results?

There has been a discrepancy among past studies with regard to the relation between negative priming and familiarity of stimuli. That is, Malley and Strayer (1995; Strayer & Grison, 1999) reported that the more familiar the stimuli were, the larger negative priming became (i.e., a positive correlation), whereas DeSchepper and Treisman (1996; Treisman & DeSchepper, 1996) reported that the less familiar the stimuli were, the larger negative priming became (i.e., a negative correlation). These studies differ not only in their experimental tasks (identification vs. matching) but also in their respective manners of arranging unfamiliar stimuli (pure vs. mixed). In the present study, using an identical set of stimuli, we examined whether these factors caused the opposite results. An identification task with a pure arrangement produced a positive correlation, and a matching task with a mixed arrangement produced a negative correlation. These results suggest that the past opposing results are both replicable and that they have reflected the different causal mechanisms of negative priming.     

Negative identity priming is contingent on stimulus repetition

Five experiments demonstrate that negative identity priming is contingent on stimulus repetition. In ignored repetition conditions, priming was initially positive and became negative as the number of repetitions increased. Moreover, it was repetition as a target, not as a distractor, that was critical for negative priming. The effects of repetition were general: They were found with both naming and same-different paradigms, verbal and pictorial material, familiar and unfamiliar stimuli, and vocal and manual responses. Findings support an activation-based model of negative priming (G. B. Malley & D. L. Strayer, 1995) and are problematic for the episodic retrieval model of negative priming (W. T. Neill & L. A. Valdes, 1992). Finally, the experiments did not replicate B. DeSchepper and A. Treisman's (1996) reported negative priming with nonrepeated novel shapes.     

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.     

Negative priming for spatial location?

The term negative priming has been used to describe the deleterious consequences for performance when the current target shares properties with an ignored distractor from the previous trial. Location-based negative priming was first reported by Tipper, Brehaut, and Driver (1990) who used a prime-probe procedure wherein the task was to localize targets defined by their identity (shape). Design imbalances in this seminal study, and others, are illustrated and it is indicated how these might have contaminated the reported effects. The findings, from three experiments using an unbiased design, suggest that negative priming in the spatial location procedure may be more closely related to inhibition of return (IOR), or to the automatic attraction of attention by new objects, than to the concepts of distractor inhibition, episodic retrieval, and feature mismatch, which have traditionally been used to explain negative priming for spatial location.     

Perceptual and response components in repetition priming of spoken words and pseudowords

Two experiments explored repetition priming effects for spoken words and pseudowords in order to investigate abstractionist and episodic accounts of spoken word recognition and repetition priming. In Experiment 1, lexical decisions were made on spoken words and pseudowords with half of the items presented twice (～12 intervening items). Half of all repetitions were spoken in a “different voice” from the first presentations. Experiment 2 used the same procedure but with stimuli embedded in noise to slow responses. Results showed greater priming for words than for pseudowords and no effect of voice change in both normal and effortful processing conditions. Additional analyses showed that for slower participants, priming is more equivalent for words and pseudowords, suggesting episodic stimulus–response associations that suppress familiarity-based mechanisms that ordinarily enhance word priming. By relating behavioural priming to the time-course of pseudoword identification we showed that under normal listening conditions (Experiment 1) priming reflects facilitation of both perceptual and decision components, whereas in effortful listening conditions (Experiment 2) priming effects primarily reflect enhanced decision/response generation processes. Both stimulus–response associations and enhanced processing of sensory input seem to be voice independent, providing novel evidence concerning the degree of perceptual abstraction in the recognition of spoken words and pseudowords.     

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.     

Cross-language positive priming disappears, negative priming does not: Evidence for two sources of selective inhibition

The authors used a unilingual and bilingual primed lexical decision task to investigate priming effects produced by attended and ignored words. In the unilingual experiment, accelerated lexical decisions to probe target words resulted when the word matched the preceding target word, whereas slowed lexical decisions to probe target words resulted when the word matched the preceding ignored nontarget word. In the bilingual (English-Spanish) experiment, between-language, rather than within-language, priming manipulations were used. Although the ignored repetition negative priming effect replicated across languages, cross-language attended repetition positive priming did not. This dissociation of priming effects in the inter- versus intralanguage priming conditions contradicts episodic retrieval accounts of negative priming that deny the existence of selective inhibitory processes. On the other hand, these results support an extension of inhibition-based accounts of negative priming, because they indicate that inhibition can operate at two levels of abstraction--local word and global language--simultaneously.     

Negative priming with masked distractor-only prime trials: awareness moderates negative priming

The literature yields inconsistent evidence for negative priming (NP) following masked distractor-only prime trials. We contrast two different hypotheses on the inconsistent findings: one - which is most compatible with the temporal discrimination theory - that relates the sign of priming effects to the absence vs. presence of prime awareness and one -which is most compatible with the inhibition and episodic retrieval accounts - that relates the sign of priming effects to the prime event being categorized as a to-be-attended vs. to-be-ignored event. In two experiments, it turned out that participants' awareness of the masked stimuli caused the different results (with participants being not aware of the primes showing NP), whereas the factor prime color = probe target color vs. prime color = probe distractor color (i.e., the prime contains the to-be-attended vs. the to-be-ignored signal) did not moderate NP. These findings are discussed with regard to theories of negative priming and the debate on conscious vs. unconscious perception.     

Episodic accessibility and morphological processing: evidence from long-term auditory priming

Long-term priming studies of lexical processing have yielded conflicting claims as to whether abstract versus episodic representations are involved during word recognition. A critical piece of evidence that could separate the two accounts rests on the existence of full morphological priming, where morphologically related words yield the same amount of priming as repeated words. In this study, participants performed speeded lexical decision on lists of auditory words and non-words, which contained repeated, morphologically related, semantically related and phonologically related pairs of items. In order to minimize the involvement of episodic factors, we increased the prime-target interval and decreased their physical similarity by introducing a change in speaker’s voice. We show that under conditions that minimize access to episodic features, the magnitude of repetition priming decreased to attain that of morphological priming. Importantly, morphological and repetition priming for words were always observed in the absence of any semantic and phonological priming, suggesting that they cannot be reduced to formal or meaning overlap. Our results support the view that long-term priming taps both abstract lexical codes with a morphological format and episodic memory components. Further, they show that episodic influences on priming can be modulated by prime-target interval and physical similarity.     

Bigger than a breadbox? Attention to distractors may not enhance negative priming

In several recent studies, P. A. MacDonald and colleagues (e.g., P. A. MacDonald & S. Joordens, 2000) reported unusually large negative priming effects and claimed that attention to distractors, counter to expectations, served to enhance the magnitude of the effect. In 3 experiments using their novel comparative judgment task, negative priming was assessed using both a control condition based on that of P. A. MacDonald, S. Joordens, and K. N. Seergobin (1999) and one in which control probe items exactly matched those on ignored repetition trials. In MacDonald et al.'s unmatched control condition, participants were faster than on ignored repetition trials, but this difference was reduced or absent when control items were matched. This result led to the conclusion that the apparently large negative priming effect reported by MacDonald and colleagues may be an artifact arising because judgments for a subset of their control trials were relatively easier than for ignored repetition trials.     

On the time course of negative priming: Another look

In two experiments, the pattern of persistence of negative priming effects across delay intervals of 500 and 2,500 msec was assessed using a within-subjects, random sequencing of delays. Neill and Valdes (1992; Neill, Valdes, Terry, & Gorfein, 1992) have argued that a within-subject experimental design is required for decay of negative priming to be seen, in contrast to results reported elsewhere (e.g., Tipper, Weaver, Cameron, Brehaut, & Bastedo, 1991) showing stable negative priming effects across delays. In neither experiment was substantial evidence of decay detected, raising questions for the notion that suppression necessarily declines across brief temporal intervals and for the assertion that episodic retrieval is the sole source of negative priming.     

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.     

Auditory negative priming in younger and older adults

Two experiments are reported in which performance of old and young adults in an auditory negative priming task was compared. Auditory negative priming was not smaller in old than in young adults. This result was independent of whether or not conditions were present that had previously been assumed to favour episodic retrieval, as opposed to inhibitory processes, as a basis of the negative priming phenomenon. The data from the present auditory negative priming experiments are incompatible with the global assumption that the efficiency of inhibitory attentional processes in general diminishes across the adult life span.     

Negative priming 1985 to 2015: a measure of inhibition,the emergence of alternative accounts,and the multiple process challenge

In this article, three generations of authors describe the background to the original article; the subsequent emergence of vigorous debates concerning what negative priming actually reflects, where radically different accounts based on memory retrieval were proposed; and a re-casting of the conceptual issues underlying studies of negative priming. What started as a simple observation (slowed reaction times) and mechanism (distractor inhibition) appears now to be best explained by a multiple mechanism account involving both episodic binding and retrieval processes as well as an inhibitory process. Emerging evidence from converging techniques such as functional magnetic resonance imaging (fMRI), and especially electroencephalography (EEG), is beginning to identify these different processes. The past 30 years of negative priming experiments has revealed the dynamic and complex cognitive processes that mediate what appear to be apparently simple behavioural effects.     

A critical evaluation of cognitive inhibition in dissociative identity disorder as inferred by negative priming in the flanker task: Limitations and the episodic retrieval alternative

Studies examining negative priming in dissociative identity disorder (DID) using the flanker task have reported emotional context effects. Significant negative priming is evident when individuals with DID are assessed in a context deemed emotionally neutral, while in contexts designed to elevate anxiety, DID samples display reduced negative priming. Limitations and considerations are discussed around statistical power, generalizability and reliability, and the use of diagnostic groups over specific clinical symptoms. The negative priming findings in this growing body of work have been interpreted with reference to the functioning of cognitive inhibitory mechanisms. Explored is how the episodic retrieval account of negative priming, with its reliance on memory mechanisms, could account for the DID findings. Encoding and retrieval possibilities are discussed and it is concluded that a failure to encode the prime trial distractor stimulus, in contexts of heightened anxiety, could explain the experimental findings from an episodic retrieval perspective.     

Repeated Repetition Priming in Face Recognition

Prior exposure to an item can facilitate subsequent recognition of that item. This effect, known as repetition priming, has been found for the recognition of many stimuli including faces (Bruce & Young, 1986). Three experiments are reported, which investigated whether repetition priming is limited to the first repetition or whether subsequent repetitions continually act to increase the speed of face processing. Experiment 1 demonstrated that repetition can reduce categorization time for faces after the first exposure, and this effect is independent of practice effects. Experiment 2 demonstrated that the relationship between reaction time and number of repetitions fits a negative power function. Experiment 3 investigated how delay affects this power function. Delay was found to decrease the negative gradient of the power curve. The effects of priming and delay are discussed in terms of the predictions made by Burton's (1994) interactive activation and competition with learning (IACL) model of face recognition and accounts of automaticity.     

Affective priming with subliminally presented pictures.

Affective priming studies have demonstrated that subliminally presented prime words can exert an influence on responses towards positive or negative target stimuli. In the present series of experiments, it was investigated whether these findings can be extended to pictorial stimuli. Ideographically selected positive, neutral, and negative picture primes that were sandwich-masked immediately preceded positive or negative target pictures (Experiment 1) or words (Experiments 2 & 3). Evaluative categorization responses to these target stimuli were significantly influenced by the valence of the prime. First, it was demonstrated that high anxious participants were selectively slowed when the subliminally presented prime was negative (Experiments 1 & 2). Second, the affective congruence between primes and targets also exerted an influence on the responses, but in a direction that is opposite to what is typically observed in affective priming research. These reverse priming effects are situated within a series of recent similar findings, and implications for theories of affective priming are discussed.     

The control of visual attention and its influence on prioritized processing in a location negative priming paradigm

In a location-based negative priming paradigm, the possibility of a disengagement option of the underlying inhibitory mechanism was tested. Whereas in previous studies disengagement was observed when providing utility information about the probe trial structure, in the present study the allocation of visual attention to the stimuli was manipulated. In the first step an automatic deployment of visual attention was implemented by presenting all stimuli as abrupt onsets (Experiment 1), which demonstrated commonly observed negative priming effects. In further conditions of non-automatic allocation of visual attention in which target and distractor were presented as no-onset stimuli, negative priming effects were eliminated (Experiments 2 and 3). The preferred interpretation is that in conditions of automatic control of attention, target and distractor compete for control of action. A non-automatic control of visual attention, on the other hand, leads to a top-down modulated selection, which results in prioritized target encoding and a loss of distractor impact on the selection process. Alternative accounts and the role of no-onset distractor processing were investigated in Experiment 4.