Mask-induced priming and the negative compatibility effect

Under certain conditions, masked primes have produced counter-intuitive negative compatibility effects (NCE), such that RT is increased, not decreased, when the target is similar to the prime. This NCE has been interpreted as an index of automatic motor inhibition, triggered to suppress the partial motor activation caused by the prime. An alternative explanation is that perceptual interactions between prime and mask produce positive priming in the opposite direction to the prime, explaining the NCE without postulating inhibition. Here the potential role of this "mask-induced priming" was investigated in two experiments, using masks composed of random lines. Experiment 1 compared masks that included features of the primes and targets with masks that did not. The former should create more mask-induced priming, but the NCE did not differ between masks. Experiment 2 employed masks that contained features of either one target or the other, but not both. These asymmetric masks produced significant mask-induced priming, but it was insufficient in size to account for the prime-related NCE. Thus mask composition can contribute to NCEs, but when random line masks are employed, the major source of the NCE seems to be motor-inhibition.     

Spatial stimulus-response compatibility and negative priming

According to Kornblum's (1992) dimensional overlap model, when an incongruent response to a stimulus is required, automatic activation of the congruent response must first be inhibited. Shiu and Kornblum (1996a) provided evidence for such inhibition in an incongruent symbolic negative priming task. Reaction time was longer when a trial's correct response was the name of the stimulus from the previous trial than when it was not. We report three experiments that test this inhibition hypothesis for spatial stimuli and responses. In Experiment 1, which used a spatial mapping analogous to the symbolic mapping used by Shiu and Kornblum (1996a), a similar negative priming effect was found. However, in Experiments 2 and 3, which used mappings that were conducive to simple transformational rules, a positive priming effect was obtained. The results suggest that inhibition in response selection may depend on the complexity of the relations between the stimuli and responses.     

The negative priming effect: Inhibitory priming by ignored objects

A priming paradigm was employed to investigate the processing of an ignored object during selection of an attended object. Two issues were investigated: the level of internal representation achieved for the ignored object, and the subsequent fate of this representation. In Experiment 1 a prime display containing two superimposed objects was briefly presented. One second later a probe display was presented containing an object to be named. If the ignored object in the prime display was the same as the subsequent probe, naming latencies were impaired. This effect is termed negative priming. It suggests that internal representations of the ignored object may become associated with inhibition during selection. Thus, selection of a subsequent probe object requiring these inhibited representations is delayed. Experiment 2 replicated the negative priming effect with a shorter inter-stimulus interval. Experiment 3 examined the priming effects of both the ignored and the selected objects. The effect of both identity repetition and a categorical relationship between prime and probe stimuli were investigated. The data showed that for a stimulus selected from the prime display, naming of the same object in the probe display was facilitated. When the same stimulus was ignored in the prime display, however, naming of it in the probe display was again impaired (negative priming). That negative priming was also demonstrated with categorically related objects suggests that ignored objects achieve categorical levels of representation, and that the inhibition may be at this level.     

The amygdala is involved in affective priming effect for fearful faces

The object of this study was to investigate whether the amygdala is involved in affective priming effect after stimuli are encoded unconsciously and consciously. During the encoding phase, each masked face (fearful or neutral) was presented to participants six times for 17ms each, using a backward masking paradigm. During the retrieval phase, participants made a fearful/neutral judgment for each face. Half of the faces had the same valence as that seen during encoding (congruent condition) and the other half did not (incongruent condition). Participants were divided into unaware and aware groups based on their subjective and objective awareness assessments. The fMRI results showed that during encoding, the amygdala elicited stronger activation for fearful faces than neutral faces but differed in the hemisphere according to the awareness level. During retrieval, the amygdala showed a significant repetition priming effect, with the congruent faces producing less activation than the incongruent faces, especially for fearful faces. These data suggest that the amygdala is important in unconscious retrieving of memories for emotional faces whether they are encoded consciously or unconsciously.     

Semantic priming of familiar faces

A series of experiments to explore the effect of priming by semantically related items in familiarity judgement tasks using faces and names that are analogous to lexical decision tasks is reported. In the first experiment, the semantic priming effect in face recognition reported by Bruce (1983) was explored in more detail by including neutral as well as associated and unrelated primes and by varying the prime-target SOA from 250 to 1,000 msec. Significant facilitation effects, with no inhibition, were found at all three SOAs. To explore the analogy between the processing of faces and verbal materials, a second experiment used names rather than faces. The difference between related and unrelated conditions at 250- and 1,000-msec SOA was similar to that found for faces in Experiment 1, but for names there was some evidence of inhibition. To investigate the locus of the priming effect with faces, in Experiment 3 the effect of degrading face targets was examined. An interaction between stimulus quality and semantic priming was observed, suggesting that the locus of the facilitation might lie at a relatively early stage in face processing. The results of these experiments illustrate further similarities between the processing of faces and verbal materials (cf. Bruce 1979, 1981).     

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.     

The effect of emotional faces on eye movements and attention

Using a rapid serial visual presentation (RSVP) paradigm, response times to a previously ignored item occurring after a target were measured. Using this procedure, it was possible to plot the time course of inhibition following target selection. Results showed that post-target distractors produce negative priming for at least 270 ms after target presentation. It is suggested that stimuli presented immediately after a target may be inhibited in order to prevent temporal binding errors. The results are discussed in relation to two selective attention paradigms: negative priming and the attentional blink.     

Repetition priming from moving faces

Recent experiments have suggested that seeing a familiar face move provides additional dynamic information to the viewer, useful in the recognition of identity. In four experiments, repetition priming was used to investigate whether dynamic information is intrinsic to the underlying face representations. The results suggest that a moving image primes more effectively than a static image, even when the same static image is shown in the prime and the test phases (Experiment 1). Furthermore, when moving images are presented in the test phase (Experiment 2), there is an advantage for moving prime images. The most priming advantage is found with naturally moving faces, rather than with those shown in slow motion (Experiment 3). Finally, showing the same moving sequence at prime and test produced more priming than that found when different moving sequences were shown (Experiment 4). The results suggest that dynamic information is intrinsic to the face representations and that there is an advantage to viewing the same moving sequence at prime and test.     

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.     

Hemisphere differences in the mood state-dependent effect for recognition of emotional faces

Forty subjects viewed 10 pictures of facial expressions of emotion while they experienced a happy mood and 10 pictures while they experienced a sad mood. Later, while re-experiencing either a happy or sad mood, they were tested for recognition of these 20 target pictures intermixed with 20 distractors. Recognition of the 10 pictures seen earlier in a disparate mood was impaired significantly when they were presented at testing to the right hemisphere, but not when presented to the left. The right hemisphere appears to store the subject's mood as an integral part of a memory representation for an emotionally expressive face. When that face is presented at testing to the right hemisphere, recognition depends on whether the subject's test mood matches the mood stored in the representation. In contrast, the left hemisphere appears to store the subject's mood separately from encoded visual information about a face, and so recognition of a face presented at testing to the left hemisphere is unaffected by changes in mood.     

Perceptual and motor contributions to the negative compatibility effect

The current study focused on contributions to the negative compatibility effect (NCE) from object-updating at the perceptual level and self-inhibition (i.e., automatic motor inhibition) at the response (motor) level. We hypothesized that contributions to the NCE from these two levels were moderated by the strength of stimulus and reaction (S–R) link: object-updating should have greater impact on the NCE with weak S–R links, but both object-updating and self-inhibition should impact on the NCE when the S–R links became strong. To test this hypothesis, in two experiments we used a novel type of stimuli and manipulated mask relevance (relevant versus irrelevant mask) and prime/target compatibility. Participants performed two tasks over three successive days. Results showed that under equivalent masking effectiveness between the two conditions of mask, a significant NCE was observed only in the relevant mask condition when the S–R links were weak, but both close to equal NCE sizes were observed in the two mask conditions when the S–R links were acquired through practice. The results indicated that perceptual and motor contributions to the NCE were moderated by the strength of S–R links, if the strength of the links was too weak to trigger the following inhibition, the NCE primarily originated from object-updating at the perceptual level; if the strength of the links was reinforced by practice, which exceeded the inhibitory threshold, the NCE originated from both object-updating and self-inhibition, but the latter was primarily responsible.     

The locus and modulation of the location negative priming effect

Responding to the location of a target is slower when it appears at a recent distractor location [ignored-repetition (IR) trial] than when it arises at a new position [control (CO) trial], defining the location negative priming (NP) effect. On IR trials, both the distractor location and response are from the prior trial, and the locus question asks whether the delayed responding that arises is caused by the reused distractor position (i.e., a location locus) or the need to execute a distractor output (i.e., a response locus). A location NP procedure was used, incorporating a many:1 location-to-response mapping design, along with a response cue on some trials. A response locus for the location NP effect was indicated. Distractor-turned-target responses took longer to initiate than new outputs (many:1 paradigm), and valid response cues reduced distractor response interference and the location NP effect. Importantly, a possible S-R compatibility problem within the many:1 S-R paradigm was not supported.     

Spatial negative priming in bilingualism

Balanced bilinguals have been shown to have an enhanced ability to inhibit distracting information. In this study, we investigated the hypothesis that the bilinguals’ efficiency in inhibitory control can be advantageous in some conditions, but disadvantageous in others—for example, negative priming conditions, in which previously irrelevant information becomes relevant. Data collected in a target-stimulus locating task from 29 early bilingual adults and 29 age-matched monolinguals showed that the bilinguals’ greater inhibition of irrelevant spatial information (i.e., the position of a distractor stimulus) resulted in a smaller effect of the distractor presence (i.e., a smaller difference in error rates in trials with and without distractors) and a larger negative priming effect (i.e., a larger difference between the error rates shown in trials wherein the target position corresponded to the position of the previous-trial distractor and trials wherein the target was presented in a previously vacant position). These findings support the hypothesis of specific nonlinguistic cognitive effects of bilingualism on inhibitory control functions, which are not necessarily reflected in cognitive advantages.     

Intended emotions influence intentional binding with emotional faces: Larger binding for intended negative emotions

The effect of emotions on Intentional binding (IB) is equivocal. In addition, most studies on IB have not manipulated emotional content of intentions. This study investigates the effect of intended and outcome emotions using emotional faces (happy or disgust face in experiment 1 and a happy or angry face in experiment 3). To see whether the effects are due to priming, we used instructions with a happy-disgust pair in experiment 2 and happy-angry pair in experiment 4. Outcome emotional faces were not predictable. Results showed that intending a negative emotional face resulted in shorter action-outcome interval judgments compared to a happy face irrespective of the emotional content of the outcome face. This effect was absent in experiments 2 and 4 with instructed emotions. In addition to showing the importance of having explicit intentions, the results show that emotional content of our intentions does influence IB possibly due to prospective mechanisms.     

Response-retrieval and negative priming

The existence of across-notation automatic numerical processing of two-digit (2D) numbers was explored using size comparisons tasks. Participants were Arabic speakers, who use two sets of numerical symbols—Arabic and Indian. They were presented with pairs of 2D numbers in the same or in mixed notations. Responses for a numerical comparison task were affected by decade difference and unit-decade compatibility and global distance in both conditions, extending previous findings with Arabic digits (Nuerk, Weger, & Willmes, 2001). Responses for a physical comparison task were affected by congruency with the numerical size, as indicated by the size congruency effect (SiCE). The SiCE was affected by unit-decade compatibility but not by global distance, thus suggesting that the units and decades digits of the 2D numbers, but not the whole number value were automatically translated into a common representation of magnitude. The presence of similar results for same- and mixed-notation pairs supports the idea of an abstract representation of magnitude.     

Stimulus-feature specific negative priming

We report the results of two experiments that showed that the time needed to respond to a feature of a stimulus increases when that particular feature of that particular stimulus previously had to be ignored. The data of Experiment 2 argue against the hypothesis that the observed stimulus-feature specific negative priming was due to a response conflict instigated by automatic episodic retrieval of prime responses. Experiment 2 also showed that the effects were not caused by difficulties in switching between prime and probe tasks and provided additional evidence for the fact that priming effects were stimulus-feature specific. The present results suggest that the selective inhibition or episodic encoding mechanisms that are assumed to underlie negative priming can operate in a more specific and powerful manner than has been previously assumed.     

Visual search for emotional faces in children

The ability to rapidly detect facial expressions of anger and threat over other salient expressions has adaptive value across the lifespan. Although studies have demonstrated this threat superiority effect in adults, surprisingly little research has examined the development of this process over the childhood period. In this study, we examined the efficiency of children's facial processing in visual search tasks. In Experiment 1, children (N=49) aged 8 to 11 years were faster and more accurate in detecting angry target faces embedded in neutral backgrounds than vice versa, and they were slower in detecting the absence of a discrepant face among angry than among neutral faces. This search pattern was unaffected by an increase in matrix size. Faster detection of angry than neutral deviants may reflect that angry faces stand out more among neutral faces than vice versa, or that detection of neutral faces is slowed by the presence of surrounding angry distracters. When keeping the background constant in Experiment 2, children (N=35) aged 8 to 11 years were faster and more accurate in detecting angry than sad or happy target faces among neutral background faces. Moreover, children with higher levels of anxiety were quicker to find both angry and sad faces whereas low anxious children showed an advantage for angry faces only. Results suggest a threat superiority effect in processing facial expressions in young children as in adults and that increased sensitivity for negative faces may be characteristic of children with anxiety problems.     

The effect of face inversion on the detection of emotional faces in visual search

Past literature has indicated that face inversion either attenuates emotion detection advantages in visual search, implying that detection of emotional expressions requires holistic face processing, or has no effect, implying that expression detection is feature based. Across six experiments that utilised different task designs, ranging from simple (single poser, single set size) to complex (multiple posers, multiple set sizes), and stimuli drawn from different databases, significant emotion detection advantages were found for both upright and inverted faces. Consistent with past research, the nature of the expression detection advantage, anger superiority (Experiments 1, 2 and 6) or happiness superiority (Experiments 3, 4 and 5), differed across stimulus sets. However both patterns were evident for upright and inverted faces. These results indicate that face inversion does not interfere with visual search for emotional expressions, and suggest that expression detection in visual search may rely on feature-based mechanisms.     

Short-term memory for emotional faces in dysphoria

The study aimed to determine if the memory bias for negative faces previously demonstrated in depression and dysphoria generalises from long- to short-term memory. A total of 29 dysphoric (DP) and 22 non-dysphoric (ND) participants were presented with a series of faces and asked to identify the emotion portrayed (happiness, sadness, anger, or neutral affect). Following a delay, four faces were presented (the original plus three distractors) and participants were asked to identify the target face. Half of the trials assessed memory for facial emotion, and the remaining trials examined memory for facial identity. At encoding, no group differences were apparent. At memory testing, relative to ND participants, DP participants exhibited impaired memory for all types of facial emotion and for facial identity when the faces featured happiness, anger, or neutral affect, but not sadness. DP participants exhibited impaired identity memory for happy faces relative to angry, sad, and neutral, whereas ND participants exhibited enhanced facial identity memory when faces were angry. In general, memory for faces was not related to performance at encoding. However, in DP participants only, memory for sad faces was related to sadness recognition at encoding. The results suggest that the negative memory bias for faces in dysphoria does not generalise from long- to short-term memory.     

Attentional capture by emotional faces in adolescence

Poor decision making during adolescence occurs most frequently when situations are emotionally charged. However, relatively few studies have measured the development of cognitive control in response to emotional stimuli in this population. This study used both affective (emotional faces) and non-affective (letter) stimuli in two different flanker tasks to assess the ability to ignore task-irrelevant but distracting information, in 25 adults and 25 adolescents. On the non-emotional (letter) flanker task, the presence of incongruent flanking letters increased the number of errors, and also slowed participants’ ability to identify a central letter. Adolescents committed more errors than adults, but there were no age-related differences for the reaction time interference effect in the letter condition. Post-hoc testing revealed that age-related differences on the task were driven by the younger adolescents (11-14 years); adults and older adolescents (15-17 years) were equally accurate in the letter condition. In contrast, on the emotional face flanker task, not only were adolescents less accurate than adults but they were also more distracted by task-irrelevant fearful faces as evidenced by greater reaction time interference effects. Our findings suggest that the ability to self-regulate in adolescents, as evidenced by the ability to suppress irrelevant information on a flanker task, is more difficult when stimuli are affective in nature. The ability to ignore irrelevant flankers appears to mature earlier for non-affective stimuli than for affective stimuli.