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.     

Negative priming and sequence learning

Three experiments used a novel sequence learning task, in which participants responded to changes in location of one visual stimulus whilst ignoring another. Experiment 1 demonstrated negative priming effects in this task, in that responses to individual sequence elements were disrupted when the attended stimulus (e.g., red asterisk) appeared at the location taken by the unattended stimulus (e.g., blue asterisk) on the immediately preceding trial. Experiments 2 and 3 found that negative priming effects extended beyond sensitivity to individual items, suggesting that people may be able to learn about sequential features of ignored events as well as about single events in isolation. The results are discussed in relation to current theories of negative priming.     

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.     

无掩蔽启动范式下负相容效应的时间进程

已有研究采用掩蔽启动范式证明了负相容效应的存在,但目前对于负相容效应的产生是否依赖于掩蔽刺激还存在激烈的争议。实验共32名大学生被试,采用12个选自汉语情感词语系统的汉字词语为材料,在显示屏刷新率为70HZ的无掩蔽启动范式下操纵启动与目标的时间间隔,让被试对目标词语的效价做出按键反应,记录被试对目标的反应时和错误率。本研究试图基于该时间进程下负相容效应发生的关键点来研究上述争议。结果发现：（1）无掩蔽范式下也存在负相容效应;（2）刺激呈现方式不同相容效应也不同。这表明负相容效应的产生并不依赖于掩蔽的呈现,且刺激的呈现方式对该效应有重要影响。     

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.     

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.     

Repeating a strongly masked stimulus increases priming and awareness

Previous studies [Marcel, A. J. (1983). Conscious and unconscious perception: Experiments on visual masking and word recognition. Cognitive Psychology, 15(2), 197–237; Wentura, D., & Frings, C. (2005). Repeated masked category primes interfere with related exemplars: New evidence for negative semantic priming. Journal of Experimental Psychology: Learning, Memory, and Cognition, 31(1), 108–120] suggested that repeatedly presenting a masked stimulus improves priming without increasing perceptual awareness. However, neural theories of consciousness predict the opposite: Increasing bottom-up strength in such a paradigm should also result in increasing availability to awareness. Here, we tested this prediction by manipulating the number of repetitions of a strongly masked digit. Our results do not replicate the dissociation observed in previous studies and are instead suggestive that repeating an unconscious and attended masked stimulus enables the progressive emergence of perceptual awareness.     

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.     

Deeper processing at target selection increases the magnitude of negative priming

Do deeper levels of processing produce equivalent priming effects at all stages of task performance? In Experiment 1, we varied the level of processing factorially across two task stages—target selection and response selection. Each stage required perceptual (e.g., color) or conceptual (e.g., friendliness) processing of stimulus items (i.e., animal names). Negative priming was substantially greater when deeper processing was required at thetarget selection stage, but it was unaffected by the level of processing at the response selection stage. In contrast, positive priming was greater when deeper processing was required at theresponse selection stage, but it was unaffected by processing at the target selection stage. In Experiment 2, we generalized this finding using a task in which numeric targets were selected on the basis of their parity. As in Experiment 1, the deeper level of processing at the target selection stage produced a larger negative priming effect. These results illuminate the role of target selection demands in modulating the strength of negative priming.     

Attending to the distractor and old/new discriminations in negative priming

When participants ignore an irrelevant distractor they typically show impaired responding to that item if it becomes the relevant stimulus on a subsequent trial. In Experiment 1 (N = 64), a masked white colour name was presented briefly before a Stroop display. Negative priming in colour naming occurred when the colour of the lettering for the Stroop stimulus matched the colour name displayed in the first display, consistent with the proposal of temporal discrimination theory that negative priming arises because a recurrence of an unattended stimulus cannot readily be classified as old or new. Experiment 2 (N = 32) replicated negative priming in the interleaved-word display where participants had to name the red word from a pair of red and green words. In Experiment 3 (N = 32) and Experiment 4 (N = 28) the participants were required to attend to but not respond to the words in the prime display and name one of two interleaved words in the probe display. Negative priming was observed in this arrangement, consistent with the episodic retrieval theory of negative priming. The temporal discrimination model may need to be extended to situations in which the attended stimuli have different responses attached to them.     

Where perception meets memory: A review of repetition priming in visual search tasks

What we have recently seen and attended to strongly influences how we subsequently allocate visual attention. A clear example is how repeated presentation of an object’s features or location in visual search tasks facilitates subsequent detection or identification of that item, a phenomenon known as priming. Here, we review a large body of results from priming studies that suggest that a short-term implicit memory system guides our attention to recently viewed items. The nature of this memory system and the processing level at which visual priming occurs are still debated. Priming might be due to activity modulations of low-level areas coding simple stimulus characteristics or to higher level episodic memory representations of whole objects or visual scenes. Indeed, recent evidence indicates that only minor changes to the stimuli used in priming studies may alter the processing level at which priming occurs. We also review recent behavioral, neuropsychological, and neurophysiological evidence that indicates that the priming patterns are reflected in activity modulations at multiple sites along the visual pathways. We furthermore suggest that studies of priming in visual search may potentially shed important light on the nature of cortical visual representations. Our conclusion is that priming occurs at many different levels of the perceptual hierarchy, reflecting activity modulations ranging from lower to higher levels, depending on the stimulus, task, and context—in fact, the neural loci that are involved in the analysis of the stimuli for which priming effects are seen.     

Negative priming and stimulus-response compatibility

The subjects in this study made incongruent naming responses to words and pictures that were presented on alternate trials (e.g., say “car” toBIKE). Their response time was longer if the correct response for the current trial was the name of the stimulus presented on the preceding trial, as compared with a control condition. These results suggest that the tendency to produce the (congruent) name of the stimulus is automatically activated and then inhibited. The “negative priming” effects appeared stronger for words where pictures were primes than for pictures where words were primes. The implications of these results for negative priming and stimulus-response compatibility are discussed.     

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.     

Long-term positive and negative identity priming: Evidence for episodic retrieval

An episodic retrieval account of negative priming (Neill, 1997; Neill & Valdes, 1992) was evaluated in three experiments. Duringpractice, regular word pairs were presented to subjects differing numbers of times. The subjects named specific target words while they ignored specific distractor words. Following a 5-min retention interval, memory for practice was revealed:Test responses for target words exhibited positive priming that increased with increases in the number of times that the words had been attended. Test responses for distractor words exhibited either positive priming (Experiment 1) or negative priming (Experiments 2–3) that also increased with increases in the number of times that the words had been ignored. The type of priming that abstractors exhibited was determined by several contextual similarities between the practice environment, in which distractors were ignored initially, and the test environments, in which they were processed subsequently. Negative priming that spanned a 5-min interval, increased with increases in the number of times that a distractor was ignored, and was sensitive to contextual changes indicated that the direction of the effect was temporally backward because the test probe cued memory for earlier processing of the priming stimulus when the distractor had been ignored.     

Global/local processing and negative priming: the influence of selection difficulty and stimulus exposure

Negative priming is a decrement in performance observed when a previously ignored stimulus is re-presented as a target. The present study examined the relation between selection difficulty and negative priming in five experiments that used hierarchical stimuli (large letters made up by small letters). The results show that negative priming is greater when subjects direct attention to the local level (more difficult selection) than when they direct attention to the global level (less difficult selection). However, that occurs only when exposure of prime and probe is sufficiently long. With shorter presentations, negative priming is still observed but is no longer modulated by selection difficulty. These results suggest that both anticipatory and reactive mechanisms are responsible for the occurrence of negative priming and that instantiation of the reactive mechanism depends on the time available for prime and probe selection. Received: 17 January 2000 / Accepted: 3 July 2000     

Subliminal action priming modulates the perceived intensity of sensory action consequences

The sense of control over the consequences of one’s actions depends on predictions about these consequences. According to an influential computational model, consistency between predicted and observed action consequences attenuates perceived stimulus intensity, which might provide a marker of agentic control. An important assumption of this model is that these predictions are generated within the motor system. However, previous studies of sensory attenuation have typically confounded motor-specific perceptual modulation with perceptual effects of stimulus predictability that are not specific to motor action. As a result, these studies cannot unambiguously attribute sensory attenuation to a motor locus. We present a psychophysical experiment on auditory attenuation that avoids this pitfall. Subliminal masked priming of motor actions with compatible prime–target pairs has previously been shown to modulate both reaction times and the explicit feeling of control over action consequences. Here, we demonstrate reduced perceived loudness of tones caused by compatibly primed actions. Importantly, this modulation results from a manipulation of motor processing and is not confounded by stimulus predictability. We discuss our results with respect to theoretical models of the mechanisms underlying sensory attenuation and subliminal motor priming.     

Negative priming and stimulus repetition: A reply to Neill and Joordens (2002)

Negative priming is reliably obtained with repeated items, but not with novel items. Here, we review why these stimulus repetition effects raise problems for memorybased theories of negative priming. Furthermore, we provide empirical evidence casting doubt on Neill and Joordens’s (2002) claim that perceptual facilitation masks the effects of episodic retrieval with novel items. Finally, we discuss several theoretical and methodological issues raised in the reply by Neill and Joordens. We conclude that a more straightforward interpretation of these stimulus repetition effects is one based on activation-sensitive inhibition.     

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.     

One version of direct response priming requires automatization of the relevant associations but not awareness of the prime

Priming is the influence of one event on performance during a second event. One type of priming is known as semantic priming because it biases interpretation of the subsequent stimulus. Another type, direct response priming, biases responding directly without semantic mediation. Research reviewed in this article indicates that two versions of the second type, direct response priming, can be distinguished. One version, explicit priming, requires awareness of the prime. The other version, associative response priming, occurs even if the prime is masked and not phenomenally visible. This version, which is attributed to associations relating specific sensory events to movements of particular muscles, is enabled only if the association has previously been automatized by brief practice in which the to-be-primed response is made to the stimulus that subsequently appears as the prime. Associative response priming can be explained by a simple stimulus–response interpretation; other varieties of priming are more theoretically challenging.