Task switches under Go/NoGo conditions and the decomposition of switch costs

Alternating switches between two simple S-R tasks are combined with Go/NoGo tasks. Non-switches after Go trials are assumed to selectively profit from stimulus driven repetition benefits, whereas switches after NoGo trials are assumed to be selectively delayed by stimulus driven negative priming. Intentionally driven reconfiguration costs are assessed by RT differences between switches after Go trials (no negative priming) and non-switches after NoGo trials (no repetition benefits). Experiment 1 indicates that with short preparation time repetition benefits, negative priming costs, and intentional components contribute approximately additively to switch costs. Experiment 2 confirms that the delay of switches after NoGo trials is indeed due to negative priming. Experiments 3 and 4 show that repetition benefits and intentional components of switch costs are properly assessed only if the settings assure that participants reconfigure the required task set in NoGo as well as Go trials.     

A bottleneck in face identification: repetition priming from flanker images

There is evidence that face processing is capacity-limited in distractor interference tasks and in tasks requiring overt recognition memory. We examined whether capacity limits for faces can be observed with a more sensitive measure of visual processing, by measuring repetition priming of flanker faces that were presented alongside a face or a nonface target. In Experiment 1, we found identity priming for face flankers, by measuring repetition priming across a change in image, during task-relevant nonface processing, but not during the processing of a concurrently-presented face target. Experiment 2 showed perceptual priming of the flanker faces, across identical images at prime and test, when they were presented alongside a face target. In a third Experiment, all of these effects were replicated by measuring identity priming and perceptual priming within the same task. Overall, these results imply that face processing is capacity limited, such that only a single face can be identified at one time. Merely attending to a target face appears sufficient to trigger these capacity limits, thereby extinguishing identification of a second face in the display, although our results demonstrate that the additional face remains at least subject to superficial image processing.     

Attention and repetition priming in the verb generation task

Transfer-appropriate processing (TAP) and identification–production frameworks predict that repetition priming will be reduced by encoding-phase divided attention (DA) in implicit memory tasks that involve conceptual analysis of test stimuli and require responses that go beyond the identification of the test cue. This prediction was tested using the verb generation task. Verb generation priming was weakly affected by a number classification distracting task at encoding that impacted recognition, was affected more by a more demanding mental arithmetic task, and was abolished entirely by a selective attention manipulation. Priming originating largely from a process unique to the verb generation task was also found to be attention-sensitive. DA affected priming equivalently for high-competition and low-competition items, against the identification–production framework which predicts greater DA effects on priming in high-competition conditions. The results fit comfortably within the TAP framework.     

Priming is independent of skill learning.

This study examined the relation between repetition priming and skill learning. Priming refers to facilitation in processing a specific item as a result of previous exposure to that item. Skill learning refers to general improvement in task performance as a function of practice. In Experiment 1 (N = 60), skill acquisition occurred in partial-word identification and inverted reading tasks but not in a word-fragment completion task. However, the amount of priming was the same in all three tasks. In Experiment 2 (N = 52), priming effects in partial-word identification did not vary as a function of practice with degraded words. In Experiment 3 (N = 40), skill learning was greater with high- than with low-frequency words, whereas priming was unaffected by word frequency. Experiment 4 (N = 20) ruled out the possibility that explicit retrieval was involved in the implicit memory tasks. These results suggest that priming can be independent of skill learning.     

The role of involuntary aware memory in the implicit stem and fragment completion tasks: a selective review

In this article I argue that an awareness of the study episode that arises involuntarily during an implicit stem/fragment completion test can under some conditions lead to enhanced repetition priming effects, even though subjects are not engaged in intentional retrieval. I review findings that are consistent with this possibility, which include the effects of depth of processing, and of typography match and new association priming following deep encoding. A theoretical account of involuntary aware memory couched within Moscovitch's (1995b) memory systems framework which suggests that the medial-temporal lobe/hippocampal (MTL/H) complex functions as a memory module is outlined. A putative mechanism is proposed in which involuntary aware memory of a studied item enhances the size of repetition priming effects by guiding its selection in preference to the competitors.     

Priming and stimulus-response learning in perceptual classification tasks

Participants often respond more quickly and more accurately to a repeated stimulus compared to a non-repeated one, a phenomenon known as repetition priming. In semantic classification tasks priming appears to be largely attributable to the learning of stimulus-decision and stimulus-response associations, which allow participants to bypass many of the processes engaged during initial stimulus analysis. The current study tested whether stimulus-response learning plays a similarly dominant role in priming that occurs in perceptual classification tasks. Unfamiliar objects were used as stimuli to reduce the influence of semantic processes on priming and the task switched for all test trials to eliminate stimulus-decision learning. The results showed across-task priming as measured by reaction time facilitation and improved accuracy when the response remained the same during the encoding and test phases. When the response switched, similar levels of reaction time facilitation were observed, but priming as measured by accuracy was significantly reduced and no longer significant. These findings indicate that stimulus-response learning contributes to priming in perceptual classification tasks, but does not play a dominant role. Significant stimulus-level learning that is independent of the task and response also occurs and likely indexes facilitated perceptual processing of the objects.     

Inhibition of return and repetition priming effects in localization and discrimination tasks.

Inhibition of return (IOR) refers to slower responding to a stimulus that is presented at the same, rather than a different location as a preceding, spatially nonpredictive, stimulus. Repetition priming refers to speeded responding to a stimulus that duplicates the visual characteristics of a stimulus that precedes it. IOR and repetition priming effects interact in nonspatial discrimination tasks but not in localization tasks; three experiments examined whether this is due to processing differences or due to response differences between tasks. Two stimuli, S1 and S2, occurred on each trial. In Experiment 1, S1 and S2 were both peripheral arrows; in Experiment 2, S1 was a central arrow and S2 was a peripheral nondirectional rectangle; in Experiment 3, S1 was a peripheral nondirectional rectangle and S2 was a peripheral arrow. S1 never required a response; S2 required a localization or a discrimination response. Despite evidence that form information was likely extracted from the arrow stimuli, the localization task revealed no repetition priming: IOR occurred regardless of shared visual identity of the S1 and S2 arrows. The discrimination task revealed IOR only when the visual identity changed from S1 to S2; otherwise, facilitation occurred. These results suggest that IOR is masked by repetition priming only when the response depends on the explicit processing of form information; repetition priming does not occur when such information is extracted automatically but is task (and response) irrelevant.     

Dissociating mere exposure and repetition priming as a function of word type

The mere exposure effect is defined as enhanced attitude toward a stimulus that has been repeatedly exposed. Repetition priming is defined as facilitated processing of a previously exposed stimulus. We conducted a direct comparison between the two phenomena to test the assumption that the mere exposure effect represents an example of repetition priming. In two experiments, having studied a set of words or nonwords, participants were given a repetition priming task (perceptual identification) or one of two mere exposure (affective liking or preference judgment) tasks. Repetition priming was obtained for both words and nonwords, but only nonwords produced a mere exposure effect. This demonstrates a key boundary for observing the mere exposure effect, one not readily accommodated by a perceptual representation systems (Tulving & Schacter, 1990) account, which assumes that both phenomena should show some sensitivity to nonwords and words.     

Repetition priming of access to biographical information from faces

Two experiments examined repetition priming on tasks that require access to semantic (or biographical) information from faces. In the second stage of each experiment, participants made either a nationality or an occupation decision to faces of celebrities, and, in the first stage, they made either the same or a different decision to faces (in Experiment 1) or the same or a different decision to printed names (in Experiment 2). All combinations of priming and test tasks produced clear repetition effects, which occurred irrespective of whether the decisions made were positive or negative. Same-domain (face-to-face) repetition priming was larger than cross-domain (name-to-face) priming, and priming was larger when the two tasks were the same. It is discussed how these findings are more readily accommodated by the Burton, Bruce, and Johnston () model of face recognition than by episode-based accounts of repetition priming.     

Repetition priming of access to biographical information from faces

Two experiments examined repetition priming on tasks that require access to semantic (or biographical) information from faces. In the second stage of each experiment, participants made either a nationality or an occupation decision to faces of celebrities, and, in the first stage, they made either the same or a different decision to faces (in Experiment 1) or the same or a different decision to printed names (in Experiment 2). All combinations of priming and test tasks produced clear repetition effects, which occurred irrespective of whether the decisions made were positive or negative. Same-domain (face-to-face) repetition priming was larger than cross-domain (name-to-face) priming, and priming was larger when the two tasks were the same. It is discussed how these findings are more readily accommodated by the Burton, Bruce, and Johnston (1990) model of face recognition than by episode-based accounts of repetition priming.     

Repetition priming mediated by task similarity in semantic classification

In the present study, the specificity of repetition priming between semantic classification tasks was examined using Osgood's (Osgood, Suci, & Tannenbaum, 1957) semantic space as a heuristic for determining the similarity between classifications. The classification tasks involved judging the meaning of words on semantic scales, such as pleasant/unpleasant. The amount of priming across classifications was hypothesized to decrease with increasing distance (decreasing similarity) between semantic scales in connotative semantic space. The results showed maximum repetition priming when the study and the test classifications were the same, intermediate degrees of priming when the study and the test classification scales shared loadings on semantic factors, and little priming when the study and the test classification scales loaded primarily on orthogonal semantic factors--that is, when the distance between scales was maximized. Consistent with the transfer-appropriate processing framework, repetition priming in semantic classifications was highly task specific, decreasing with increasing distance between classification scales.     

Levels of processing effects on implicit and explicit memory tasks: using question position to investigate the lexical-processing hypothesis

One interpretation of levels of processing effects (LOP) on priming in implicit tests of memory is in terms of deficits in lexical processing during shallow study tasks. In two experiments the extent of lexical processing engaged in during standard shallow encoding tasks was manipulated by placing the encoding question either before or after the target stimulus. Clear evidence was found in explicit memory tasks that placing the question after the target stimulus increased the depth of processing of words presented in shallow encoding tasks. In contrast, there was no evidence of such an effect on the priming observed in implicit memory tasks. The results suggest that the role of lexical processing in LOP effects on priming requires further specification.     

Linking sight and sound: fMRI evidence of primary auditory cortex activation during visual word recognition

We describe two studies that used repetition priming paradigms to investigate brain activity during the reading of single words. Functional magnetic resonance images were collected during a visual lexical decision task in which nonword stimuli were manipulated with regard to phonological properties and compared to genuine English words. We observed a region in left-hemisphere primary auditory cortex linked to a repetition priming effect. The priming effect activity was observed only for stimuli that sound like known words; moreover, this region was sensitive to strategic task differences. Thus, a brain region involved in the most basic aspects of auditory processing appears to be engaged in reading even when there is no environmental oral or auditory component.     

Loss of rapid phonological recoding in reading Hanja, the logographic script of Korean

The role that recent experience has in the processing of Korean Hanja characters was investigated in two masked priming experiments. Two groups of Korean native speakers that differed in their recent exposure to Hanja were asked to name single Hanja characters (targets) that were immediately preceded by masked presentations of the same characters (repetition priming), Hanja characters that were homophones of the target (homophone priming), or unrelated characters (baseline). The results showed that the group that had been less recently exposed made more errors and were slower than the group that had been the more recently exposed. Furthermore, there was no character homophone priming for the less recently exposed group, although they did show a robust repetition priming effect. On the other hand, the more recently exposed group showed both strong character repetition and homophone priming effects. We suggest that regular exposure to characters supports their rapid and automatic processing. It is argued that the different patterns of priming for the two groups were due to how rapidly the orthographic and phonological information of the prime could be resolved.     

Word frequency effect on repetition priming as a function of prime duration and delay between the prime and the target

Two experiments studied the necessary conditions for the occurrence of repetition priming and word frequency effect on priming in a lexical decision task. To examine the role of prime processing duration, the prime was presented either for 50 ms or for 700 ms, and an interfering task was introduced between the prime and the target in order to restrict the time during which the prime was effectively processed and to limit it to exactly 50 ms or 700 ms. The interstimulus interval (ISI) between the prime and the target was 1500 ms or 3000 ms in Expt 1, and 600 ms in Expt 2. With primes presented for 50 ms, repetition priming effects were not dependent on target frequency, decreased with an increase of the ISI, and were no longer significant with an ISI of 3000 ms. With primes presented for 700 ms, repetition priming was systematically larger for low‐frequency words than for high‐frequency words, and remained reliable even with an ISI of 3000 ms. Thus, a minimum of prime duration was required both for maintaining repetition priming effects over more than some hundreds of milliseconds and for the occurrence of frequency effect on repetition priming. Theoretical interpretations of these results are discussed.     

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.     

Automatic sequential response priming and intentional response preparation in choice reaction tasks: Evidence from response repetition and response cuing

This study examined the interaction of response repetition and response cuing in a finger cuing task with a short and a long cue-stimulus interval (CSI). We observed shorter reaction times (RTs) with increasing CSI and a substantial response repetition benefit. However, this benefit was abolished at the long CSI, suggesting that response cuing neutralized the repetition effect. According to additive-factors logic, the observed interaction suggests that both repetition and cuing exert their influence on a common processing stage, which we identify as the response selection stage. We argue that cuing and repetition effects are expressions of distinct mental operations: cuing is based on intentional response code activation, whereas repetition is based on sequential, automatic response code priming. Cue-based intentional code activation starts slowly and increases with CSI, but sequential response priming is independent of CSI, explaining why cuing abolishes the response repetition benefit at the long CSI.     

Sizing up the associative account of repetition priming

Three studies which test an associative account of repetition priming in a size comparison task are reported. Congruence of decision between priming and test affected performance when the priming task and test tasks were the same but not when they differed. This congruence effect was unaffected by the proportion of trials with congruent responses. Same-task priming exceeded cross-task priming even when both tasks required the same aspect of semantic knowledge. The results indicate that a component of priming is due to associations which are formed during priming and automatically activated when stimuli are repeated at test. Stimuli do not become associated with motor responses but are associated with the results of processing at a number of other levels.     

Repetition priming: Is music special?

Using short and long contexts, the present study investigated musical priming effects that are based on chord repetition and harmonic relatedness. A musical target (a chord) was preceded by either an identical prime or a different but harmonically related prime. In contrast to words, pictures, and environmental sounds, chord processing was not facilitated by repetition. Experiments 1 and 2 using single-chord primes showed either no significant difference between chord repetition and harmonic relatedness or facilitated processing for harmonically related targets. Experiment 3 using longer prime contexts showed that musical priming depended more on the musical function of the target in the preceding context than on target repetition. The effect of musical function was decreased, but not qualitatively changed, by chord repetition. The outcome of this study challenges predictions of sensory approaches and supports a cognitive approach of musical 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.