No commonality between attentional capture and attentional blink

Visual search for a unique target is impaired when a salient distractor is presented (attentional capture). This phenomenon is said to occur because attention is diverted to a distractor before it reaches the target. Similarly, perception of the second of two targets embedded in a rapid stream of nontargets is impaired, suggesting attentional deprivation due to the processing of the first target (attentional blink). We examined whether these phenomena emerge from a common underlying attentional mechanism by using correlation studies. If these phenomena share a common foundation, the magnitude of these deficits should show within-subject correlations. Participants (N?=?135) revealed significant attentional deficits during spatial and temporal capture and the attentional blink tasks. However, no significant correlation was found among these tasks. Experiment 2 (N?=?95) replicated this finding using the same procedure as that used in Experiment 1 but included another attentional blink task that required spatial switching between the two targets. Strong correlations emerged only between the two attentional blink tasks (with/without spatial switching). The present results suggest that attentional deficits during spatial and temporal capture and the attentional blink tasks reflect different aspects of attention.     

The attentional blink reveals sluggish attentional shifting in adolescents with specific language impairment

Rapid processing deficits have been the subject of much debate in the literature on specific language impairment (SLI). Hari and Renvall (2001) [Hari, R. & Renvall, H. (2001). Impaired processing of rapid stimulus sequences in dyslexia. Trends in cognitive sciences, 5, 525-532.] proposed that the source of this deficit can be attributed to sluggish attentional shifting abilities. That is, more time is required to shift attention between stimuli. To test this claim, 26 adolescents with SLI (divided into two subgroups to control for differences in non-verbal intelligence) and 14 controls were presented with a rapid serial visual presentation task. In this task participants were asked to detect two visual targets presented serially with distracter items with varying inter-target intervals (i.e., time difference between targets). This task was designed to elicit an attentional blink (AB). The AB describes the phenomenon whereby non-impaired individuals are less likely to report the second of two targets presented within 200-500ms of each other. After controlling for group differences in non-verbal intelligence, the SLI group was found to be significantly less accurate than the control group at successfully reporting the second target at inter-target intervals of 100, 200, 300, 400 and 800ms. The results were interpreted to suggest that adolescents with language impairments have an AB which differs from non-impaired individuals in both magnitude and duration.     

The attention cascade model and attentional blink

An attention cascade model is proposed to account for attentional blinks in rapid serial visual presentation (RSVP) of stimuli. Data were collected using single characters in a single RSVP stream at 10Hz [Shih, S., & Reeves, A. (2007). Attentional capture in rapid serial visual presentation. Spatial Vision, 20(4), 301-315], and single words, in both single and dual RSVP streams at 19Hz [Potter, M. C., Staub, A., & O'Connor, D. H. (2002). The time course of competition for attention: Attention is initially labile. Journal of Experimental Psychology: Human Perception and Performance, 28(5), 1149-1162]. The model adopts similar architecture of the cognitive accounts of attentional blinks and employs computational details from theories of attention gating. The model has elaborated working memory and attention control mechanism. Both bottom-up and top-down salience are explicit in the model. Quantitative fits are good and the model parameters have plausible values. The model handles stimulus competition, lag 1 sparing, intrusion errors, and magnitude of the dip; it also accounts for commonly observed effects such as stimulus similarities (local and global), target+1 blank, and stimulus salience.     

The role of the magnocellular visual pathway in the attentional blink

Visual attention has temporal limitations. In the attentional blink (AB) a stream of stimuli such as letters or digits are presented to a participant on a computer monitor at a rapid rate. Embedded in the stream are two targets that the participant must try to identify. Identification of the second target is severely impaired if it is presented within approximately 500ms of the first target. This is the 'blink' in visual attention. In this study we examined the role of the magnocellular visual pathway in the AB. This fast conducting pathway has high temporal resolution and contrast sensitivity. It is also insensitive to the direction of chromatic contrast, and this attribute was exploited in order to isolate its contributions to temporal attention. Colour defined, luminance noise masked AB streams were compared to AB streams of varying achromatic contrast. The four observers, (2F and 2M) aged between 21 and 35years, had normal visual acuity and colour vision. The colour stimuli produced a similar blink to the moderate contrast achromatic stimuli. This indicates that the magnocellular pathway does not have a privileged role in the attentional blink. We provide an explanation of previous apparently contradictory findings in terms of the role of different types of visual masking in the attentional blink.     

Viewpoint costs occur during consolidation: evidence from the attentional blink

Do the viewpoint costs incurred when naming rotated familiar objects arise during initial identification or during consolidation? To answer this question we employed an attentional blink (AB) task where two target objects appeared amongst a rapid stream of distractor objects. Our assumption was that while both targets and distractors undergo initial identification only targets are consolidated in a form that allows overt report. We presented line drawings of objects with a usual upright canonical orientation, and separately manipulated the orientation of targets and distractors. In two experiments, targets were defined by colour, whereas in a third experiment they were defined by semantic category. Target 1 orientation influenced the AB, with objects rotated by 90 degrees causing a larger second target deficit than upright and upside-down objects. However, distractor orientation did not affect the magnitude of the second target deficit, regardless of whether targets were defined by colour or semantic category. Taken together, these findings suggest that the visual representations involved in the preliminary recognition of familiar objects are viewpoint-invariant and that viewpoint costs are incurred when these objects are consolidated for report.     

Rapid allocation of temporal attention in the attentional blink paradigm

How fast can information of a first target (T1) in a rapid serial visual presentation be used for top-down allocation of attention in time? A valid cue about the temporal position of a second target (T2) was integrated into T1. The data show that 100 ms after T1 onset, T2 was identified better than without cue, raising the conditional T2 performance. T1 apparently triggers a facilitative effect of attention, known from other paradigms such as peripheral cueing.     

The more your mind wanders,the smaller your attentional blink: An individual differences study

The present studies investigate the hypothesis that individuals who frequently report experiencing episodes of mind wandering do so because they under-invest attentional/executive resources in the external environment. Here we examined whether self-reported instances of mind wandering predict the magnitude of the “attentional blink” (AB) in a rapid serial visual presentation (RSVP) task, since a prominent view is that the AB derives from an over-investment of attention in the information stream. Study 1 demonstrates that subjective reports of mind wandering in a sustained attention task have a negative predictive relation with respect to the magnitude of the AB measured in a subsequent RSVP task. In addition, using the Spontaneous and Deliberate Mind Wandering Questionnaire in Study 2, we were again able to show that trait-level mind wandering in everyday life negatively predicts AB magnitude. We suggest that mind wandering may be the behavioural outcome of an adaptive cognitive style intended to maximize the efficient processing of dynamic and temporally unpredictable events.     

Emotional facial expressions and the attentional blink: Attenuated blink for angry and happy faces irrespective of social anxiety

Although facial information is distributed over spatial as well as temporal domains, thus far research on selective attention to disapproving faces has concentrated predominantly on the spatial domain. This study examined the temporal characteristics of visual attention towards facial expressions by presenting a Rapid Serial Visual Presentation (RSVP) paradigm to high (n=33) and low (n=34) socially anxious women. Neutral letter stimuli (p, q, d, b) were presented as the first target (T1), and emotional faces (neutral, happy, angry) as the second target (T2). Irrespective of social anxiety, the attentional blink was attenuated for emotional faces. Emotional faces as T2 did not influence identification accuracy of a preceding (neutral) target. The relatively low threshold for the (explicit) identification of emotional expressions is consistent with the view that emotional facial expressions are processed relatively efficiently.     

Upshifted decision criteria in attentional blink and repetition blindness

A large number of “unawareness” phenomena have been explained and quantified in terms of sensitivity (d′) fluctuations, with very few attempts at addressing an alternative putative cause, i.e., fluctuations of subjects’ response criteria (c). Response criteria fluctuations are particularly likely under dual-task paradigms with unbalanced sensitivities (Gorea & Sagi, 2000) such as those used in evidencing attentional blink (AB) and repetition blindness (RB) phenomena. The present study inquires into whether AB and RB are indeed prone to a deviant decisional behaviour. AB and RB were studied with a yes/no task allowing the assessment of d′ and c for the detection (presence/absence) of a target letter T2 as a function of its temporal lag relative to the presentation of another (AB) or of the same (RB) letter, T1 (Experiment 1). A significant criterion increase was observed in both cases. Additional experiments demonstrate that this criterion effect is typical of these dual-task AB and RB paradigms as it is not observed in a standard contrast detection task with mixed contrasts (Experiment 2), in a “control” AB design stripped off its first task T1 (Experiment 3), or in a metacontrast experiment (Experiment 4). We propose that the observed criterion shifts are the consequence of the inherent dual-task AB and RB designs (where observers have to judge two events of unequal saliencies) and that they entail an enhancement of the AB and RB effects as long as these effects are assessed via subjective (yes/no or matching) procedures.     

Too much control can hurt: A threaded cognition model of the attentional blink

Explanations for the attentional blink (AB; a deficit in identifying the second of two targets when presented 200-500 ms after the first) have recently shifted from limitations in memory consolidation to disruptions in cognitive control. With a new model based on the threaded cognition theory of multi-tasking we propose a different explanation: the AB is produced by an overexertion of control. This overexertion is produced by a production rule that blocks target detection during memory consolidation. In addition to fitting many known effects in the literature, the model predicts that adding certain secondary tasks will decrease the AB. In Experiment 1, a secondary task is added to the AB task in which participants have to respond to a moving dot. As predicted, AB decreases. Experiment 2 expands this result by controlling for learning, and adds a second variation, rotating the first target. For this variation the model predicts an increase in AB, which is indeed what we found.     

Inhibition from blinked category labels: Combining the attentional blink and the semantic priming paradigm

In the present experiment we combined the attentional blink and the semantic priming paradigm. We used category labels as primes and category exemplars as targets. The prime stimuli were embedded into a rapid serial visual presentation (RSVP) stream and presented at varying positions after a to-be-identified stimulus, albeit the stimulus–onset asynchrony between primes and targets remained constant throughout the experiment. As a result, participants’ prime awareness was reduced in some trials although the prime duration was always at levels usually considered to elicit awareness (60 ms). After each RSVP there was a forced choice discrimination test to assess participants’ prime awareness. When subjects could not identify the prime stimuli we observed slower responses to related as compared to unrelated targets. This result confirms results found with repeated masked primes. However, whereas former studies assessed unawareness rather coarsely at the level of individual participants, here unawareness was tested on a trial-by-trial basis.     

Memory reloaded: Memory load effects in the attentional blink

When two targets are presented in rapid succession, identification of the first is nearly perfect, while identification of the second is impaired when it follows the first by less than about 700 ms. According to bottleneck models, this attentional blink (AB) occurs because the second target is unable to gain access to capacity-limited working memory processes already occupied by the first target. Evidence for this hypothesis, however, has been mixed, with recent reports suggesting that increasing working memory load does not affect the AB. The present paper explores possible reasons for failures to find a link between memory load and the AB and shows that a reliable effect of load can be obtained when the item directly after T1 (Target 1) is omitted. This finding provides initial evidence that working memory load can influence the AB and additional evidence for a link between T1 processing time and the AB predicted by bottleneck models.     

Amplification of attentional blink by distress‐related facial expressions: Relationships with alexithymia and affectivity

The present studies aimed to analyse the modulatory effect of distressing facial expressions on attention processing. The attentional blink (AB) paradigm is one of the most widely used paradigms for studying temporal attention, and is increasingly applied to study the temporal dynamics of emotion processing. The aims of this study were to investigate how identifying fear and pain facial expressions (Study 1) and fear and anger facial expressions (Study 2) would influence the detection of subsequent stimuli presented within short time intervals, and to assess the moderating influence of alexithymia and affectivity on this effect. It has been suggested that high alexithymia scorers need more attentional resources to process distressing facial expressions and that negative affectivity increases the AB. We showed that fear, anger and pain produced an AB and that alexithymia moderated it such that difficulty in describing feelings (Study 1) and externally oriented thinking (Study 2) were associated with higher interference after the processing of fear and anger at short time presentations. These studies provide evidence that distressing facial expressions modulate the attentional processing at short time intervals and that alexithymia influences the early attentional processing of fear and anger expressions. Controlling for state affect did not change these conclusions.     

The role of the magnocellular and parvocellular pathways in the attentional blink

The attentional blink refers to the transient impairment in perceiving the 2nd of two targets presented in close temporal proximity in a rapid serial visual presentation (RSVP) stream. The purpose of this study was to examine the effect on human attentional-blink performance of disrupting the function of the magnocellular pathway--a major visual-processing pathway specialized in temporal segregation. The study was motivated by recent theories that relate the attentional blink to the limited temporal resolution of attentional responses, and by a number of poorly understood empirical findings, including the effects on the attentional blink of luminance adaptation and distraction. The attentional blink was assessed for stimuli on a red background (Experiment 1), stimuli on an equiluminant background (Experiment 2), and following flicker or motion adaptation (Experiment 3), three psychophysical manipulations known to disrupt magnocellular function. Contrary to our expectations, the attentional blink was not affected by these manipulations, suggesting no specific relationship between the attentional blink and magnocellular and/or parvocellular processing.     

The attentional blink unveils the interplay between conscious perception,spatial attention and working memory encoding

Our ability to perceive two events in close temporal succession is severely limited, a phenomenon known as the attentional blink. While the blink has served as a popular tool to prevent conscious perception, there is less research on its causes, and in particular on the role of conscious perception of the first event in triggering it. In three experiments, we disentangled the roles of spatial attention, conscious perception and working memory (WM) in causing the blink. We show that while allocating spatial attention to T1 is neither necessary nor sufficient for eliciting a blink, consciously perceiving it is necessary but not sufficient. When T1 was task irrelevant, consciously perceiving it triggered a blink only when it matched the attentional set for T2. We conclude that consciously perceiving a task-relevant event causes the blink, possibly because it triggers encoding of this event into WM. We discuss the implications of these findings for the relationship between spatial attention, conscious perception and WM, as well as for the distinction between access and phenomenal consciousness.     

Visual consciousness of faces in the attentional blink: Knowledge-based effects of trustworthiness dominate over appearance-based impressions

How we perceive and evaluate other persons depends on appearance-based impressions as well as top-down information such as knowledge about someone’s character. To date, little is known about how these two sources of information affect the conscious perception of faces, about their relative contributions and possible interactions. Here, we directly compare how social-affective knowledge and visual cues of trustworthiness impact the access of faces to visual consciousness. Low- and average-trustworthy looking faces were associated with neutral or negative information about a person’s social behavior. Trustworthiness and facial expression ratings showed robust and independent effects of both sources of information during evaluations. Under conditions of reduced attention in an attentional blink task, prioritized detection of faces associated with negative as compared to neutral person knowledge was observed, whereas facial trustworthiness did not affect detection. Thus, while both factors influenced conscious perception and evaluation, only person knowledge impacted the access to consciousness.     

Evidence for mental ability related individual differences in the attentional blink obtained by an analysis of the P300 component

Attentional blink (AB) refers to impaired identification of a target (T2) when this target follows a preceding target (T1) after about 150-450 ms within a stream of rapidly presented stimuli. Previous research on a possible relation between AB and mental ability (MA) turned out to be highly ambiguous. The present study investigated MA-related individual differences in consolidation of T2 in working memory during the AB as indicated by the P300 component of the event-related potential. Thirty high (HA) and 30 low MA (LA) female participants performed an AB task while their brain activity was recorded. The AB did not differ between the two groups. HA individuals exhibited a larger P300 amplitude and longer P300 latencies during the AB suggesting higher mental effort. This higher mental effort, however, did not result in better performance presumably because of more competition between target and distractor stimuli in HA than LA individuals.     

Individuals differ in the attentional blink: Mental speed and intra-subject stability matter

The failure to correctly report two targets (“T₁”, “T₂”) that follow each other in close temporal proximity has been called the “attentional blink” (AB). The AB has, so far, mainly been studied using experimental approaches. The present studies investigated individual differences in AB performance, revealing (among further findings) a high positive correlation between the accuracies of detecting the two targets correctly (r = 0.69); and between T₂∣T₁ accuracy and psychometric intelligence (0.41 ≤ r ≤ 0.43) and RT variability in short-term and working memory (− 0.38 ≤ r ≤ − 0.45). Together, these results support important aspects of major theoretical accounts of the AB from an individual differences perspective and introduce intelligence and intra-subject stability as contributing factors in AB performance.     

On the saliency of negative stimuli: Evidence from attentional blink1

Abstract: When people are asked to detect two targets from a rapid serial visual presentation (RSVP) stream, impairment of recognition of the second target (T2) can be observed if the T2 is presented several hundred milliseconds later than the first target (T1). This phenomenon is known as attentional blink, and is considered to reflect some temporal characteristic of the attentional process. The aim of the present study was to use the attentional blink paradigm to examine whether the affective meaning of the stimuli could affect the magnitude of attentional blink. In Experiment 1, the valence of the T2 (neutral, positive, and negative) was manipulated. Significant T2 detection deficit was observed with neutral and positive T2 but not with negative T2. Experiment 2 demonstrated that non‐significant attentional blink in negative T2 in Experiment 1 could be attributed to the negative affective meaning of T2. Results are discussed in terms of the high saliency of negative information.     

The culture of perceptual expertise and the other-race effect

In our commentary, we propose that the ORE can be viewed as a form of perceptual expertise. Like experts, we recognize own-race faces at the subordinate level as individuals and novices when recognize other-race faces at the basic level of race. Applying a perceptual expertise account, we explain the ORE in terms of its cognitive, neural, and motivational factors. We suggest that by creating a culture of “other-race” expertise, improvements in other-race face recognition can be achieved.