Masking T1 difficulty: processing time and the attenional blink

When observers are presented with 2 targets in rapid succession, identification of the 1st is highly accurate, whereas identification of the 2nd is impaired at brief intertarget intervals (i.e., 200-500 ms). This 2nd-target deficit is known as the attentional blink (AB). According to bottleneck models, the AB arises because attending to the 1st target delays allocation of attention to the 2nd target. Thus, these models predict that increasing 1st-target processing time will increase the magnitude of the AB. Previous tests of this prediction have yielded mixed results. The present work suggests that one factor contributing to this uncertainty is masking of the 1st target: When this mask is omitted, processing time and AB magnitude are reliably related. These findings clarify the role of 1st-target masking in the AB and support the validity of the bottleneck account.     

Auditory attentional blink: masking the second target is necessary, delayed masking is sufficient.

When two target items (T1 and T2) are presented in rapid succession among fillers, processing T2 is often impaired. This phenomenon is known as the attentional blink (AB). Within the visual modality, this second-target deficit generally occurs only if T2 is masked by a trailing item. The current study was designed to examine whether masking of T2 also plays a critical role in the auditory AB. Results showed a reliable AB effect even when the item following T2 was replaced by silence. However, the AB deficit was abolished when T2 was the last presented stimulus. Our results suggest that, as in vision, T2 masking is necessary for the AB to take place in audition, but that masking is effective even when delayed, providing evidence that the phenomenon shares some functional mechanisms across sensory modalities.     

Does failure to mask T1 cause lag-1 sparing in the attentional blink?

The attentional blink (AB) effect demonstrates that when participants are instructed to report two targets presented in a rapid visual stimuli stream, the second target (T2) is often unable to be reported correctly if presented 200-500 msec after the onset of the first target (T1). However, if T2 is presented immediately after T1, in the conventional lag-1 position (100-msec stimulus onset asynchrony; SOA), little or no performance deficit occurs. The present experiments add to the growing literature relating the "lag-1 sparing" effect to T1 masking. Using a canonical AB paradigm, our results demonstrate that T2 performance at lag 1 is significantly reduced in the presence of T1 masking. The implications of this outcome are discussed in relation to theories of the AB.     

Warning: Attending to a mask may be hazardous to your perception

Object substitution is a type of backward masking that occurs when a mask appears during visual search for a target. We tested the hypothesis that object substitution is an overwriting process triggered by attentional selection of the mask. Impeding attentional selection of a mask by embedding it in an array of distractors eliminated object substitution. Similarly, object substitution did not occur when the mask appeared in advance of the target and, therefore, could not capture attention during search for the target. However, masking was reinstated when the mask was revealed from background contours at the moment of target onset and could therefore capture attention during search. These observations demonstrate that attentional selection of the mask is a necessary step in this type of masking and suggest that object substitution is active overwriting of unattended information triggered by selection of other visual information at a nearby location.     

Is the attentional blink effect located in short-term memory?

The attentional blink (AB) effect is characterized by a failure to detect a second target following the identification of a previous target in a RSVP stream. This effect has been attributed to capacity limitations at a central level of visual information processes. Postperceptual models suppose that the AB locus is located in short-term memory. To test this hypothesis, we investigated the influence of a short-term memory deficit on the AB effect in a patient with such a deficit. The three main results of this study are (1) the persistence of an AB effect, (2) a large number of T1 missed identifications and (3) a T2 detection deficit for a specific delay (367 ms). These results indicate that a short-term memory deficit disrupts the processing of each target (T1 and T2) but does not product an abolition of the AB effect.     

Object substitution masking and the object updating hypothesis

The object updating hypothesis of object substitution masking proposes that the phenomenon arises when the visual system fails to individuate target and mask at the level of object token representations. This hypothesis is tested in two experiments using modifications of the dot mask paradigm developed by Lleras and Moore (2003). Target—mask individuation is manipulated by the presentation of additional display items that influence the linking apparent motion seen between a target and a spatially separated mask (Experiment 1), and by the use of placeholders that maintain the target object’s presence during mask presentation (Experiment 2). Results in both cases are consistent with the updating hypothesis in showing significantly reduced masking when the conditions promoted target—mask individuation. However, in both experiments, some masking was still present under conditions of individuation, an effect we attribute to attentional capture by the mask.     

Object file continuity predicts attentional blink magnitude

When asked to identify targets embedded within a rapid consecutive stream of visual stimuli, observers are less able to identify the second target (T2) when it is presented within half a second of the first (T1); this deficit has been termed the attentional blink (AB). Rapid serial visual presentation methodology was used to investigate the relationship between the AB and object files (episodic representations implicated in object identification and perceptual constancy). An inverse linear relationship was found between the degree of object file continuity and AB magnitude. An important locus of object file continuity was the intervening stream items between T1 and T2. The results are discussed in terms of the heuristic of the object file to preserve limited attentional capacity.     

Different effects of the two types of spatial pre-cueing: what precisely is “attention” in Di Lollo’s and Enns’ substitution masking theory?

Enns and Di Lollo [Psychological Science, 8 (2), 135-139, 1997] have introduced the object substitution theory of visual masking. Object substitution masking occurs when focusing attention on the target is delayed. However, Posner (Quarterly Journal of Experimental Psychology, 32, 3-25, 1980) has already shown that attention can be directed to a target at least in two ways: intentionally (endogenously) and automatically (exogenously). We conducted two experiments to explore the effects of endogenous and exogenous cues on substitution masking. The results showed that when attention was shifted to the target location automatically (using a local peripheral pre-cue), masking was attenuated. A decrease in target identification dependent on a delay of mask offset, typical to substitution masking, was not observed. However, strong substitution masking occurred when the target location was not pre-cued or when attention was directed to the target location intentionally (using a symbolic pre-cue displayed centrally). The hypothesis of two different mechanisms of attentional control in substitution masking was confirmed.     

When the target becomes the mask: using apparent motion to isolate the object-level component of object substitution masking

J. T. Enns and V. Di Lollo (1997) discovered a new form of visual masking that they labeled object substitution masking (OSM). OSM occurs when 4 dots, presented around a target, trail in the display after target offset. The present study showed that the physical presence of the masking dots after target offset is not necessary for OSM. Instead, the continued presence of a changing high-level representation associated with the target suffices to yield OSM. Apparent motion was used to define such representation. In these experiments, the initial display offset and was followed by a 2nd display where masks appeared at new locations. Only when the spatiotemporal properties of the stimuli on the 2nd display supported the perception of the target moving and turning into the mask was OSM observed.     

Task switching mediates the attentional blink even without backward masking

When two targets are presented in rapid succession, perception of the second target is impaired at short intertarget lags (100-700 msec). This attentional blink (AB) is thought to occur only when the second target is backward masked. To the contrary, we show that task switching between the targets can produce an AB even without masking (Experiments 1 and 3). Further, we show that task switching produces an AB only when the second target does not belong to a class of overlearned stimuli such as letters or digits (Experiments 1 and 4). When the second target is masked, however, an AB is invariably obtained regardless of switching or overlearning. We propose that task switching involves a time-consuming process of reconfiguration of the visual system, during which the representation of the second target decays beyond recognition, resulting in an AB deficit. We suggest that overlearned stimuli are encoded in a form that, while maskable, decays relatively slowly, thus outlasting the delay due to reconfiguration and avoiding the AB deficit.     

Backward masking interrupts spatial attention,slows downstream processing,and limits conscious perception

The attentional blink (AB) is a difficulty in correctly processing a target when it follows one or more other targets after a short delay. When no backward mask is presented after the last critical target, there is no or little behavioral AB deficit. The mask plays an important role in limiting conscious access to target information. In this electrophysiological study, we tested the impact of masking on the deployment and engagement of attention by measuring the N2pc and P3 components in an RSVP paradigm. We found that the presence of a mask in an AB paradigm reduced the amplitude of the N2pc, P3a, and P3b components. In addition to reducing encoding in memory, masking also reduced the effectiveness of the deployment and engagement of attention on the last target. We discuss the role of these findings in the context of current masking, consciousness, and AB models.     

Seeing the light: Adapting luminance reveals low-level visual processes in the attentional blink

It is widely assumed that high-level visual processes subserve the attentional blink (AB). Recent evidence from studies of visual masking during the AB that were designed to directly test the contributions of high-level masking effects, however, have failed to provide empirical support for this position. The implication is that low-level visual processes are crucial to the AB. We tested this idea by manipulating adapting luminance in a standard AB paradigm. Consistent with the involvement of low-level neural mechanisms, the AB effect interacted with adapting luminance such that an AB was revealed only under photopic (light adapted) viewing conditions.     

Delayed attentional engagement in the attentional blink

Observers often miss the 2nd of 2 visual targets (first target [T1] and second target [T2]) when these targets are presented closely in time; the attentional blink (AB). The authors hypothesized that the AB occurs because the attentional response to T2 is delayed by T1 processing, causing T2 to lose a competition for attention to the item that follows it. The authors investigated this hypothesis by determining whether the AB is attenuated when T2 is precued. The results from 4 experiments showed that the duration and magnitude of the AB were substantially reduced when T2 was precued. The observed improvement in T2 report did not occur at the expense of T1 report, suggesting that processing of T1 was already completed or was at least protected when the cue was presented. The authors conclude that, during the AB, there is a delay between detection and the selection of target candidates for consolidation in short-term memory.     

Recovery from object substitution masking induced by transient suppression of visual motion processing: a repetitive transcranial magnetic stimulation study

Object substitution masking is a form of visual backward masking in which a briefly presented target is rendered invisible by a lingering mask that is too sparse to produce lower image-level interference. Recent studies suggested the importance of an updating process in a higher object-level representation, which should rely on the processing of visual motion, in this masking. Repetitive transcranial magnetic stimulation (rTMS) was used to investigate whether functional suppression of motion processing would selectively reduce substitution masking. rTMS-induced transient functional disruption of cortical area V5/MT+, which is important for motion analysis, or V1, which is reciprocally connected with V5/MT+, produced recovery from masking, whereas sham stimulation did not. Furthermore, masking remained undiminished following rTMS over the region 2 cm posterior to V5/MT+, ruling out nonspecific effects of real stimulation and confirming regional specificity of the rTMS effect. The results suggest that object continuity via the normal function of the visual motion processing system might in part contribute to this masking. The relation of these findings to the reentrant processing view of object substitution masking and other visual phenomena is discussed.     

The effect of target contrast on the attentional blink

In this set of five rapid serial visual presentation experiments, observers identified one or two target letters that were embedded in a stream of distractors. Target contrasts were varied, and their effects on the attentional blink (AB) were examined. Target identification improved when its contrast was increased. But whereas an increase in the first target's (T1) contrast facilitated its identification, the recovery of the second target (T2) was paradoxically hampered (Experiments 2 and 5). Similarly, identification of the target suffered when the preceding singleton's contrast was increased (Experiment 1). The AB was eliminated by inserting a blank after a low-contrast, but not a high-contrast, T1 (Experiment 5). Increasing T2's contrast attenuated the blink (Experiment 3) and compensated the larger AB caused by a high-contrast T1 (Experiment 4). In all, these results showed that attention continued to be engaged as long as the target's contrast prolonged its perceptibility. When the high-contrast target was T1, a larger AB was produced; when it was T2, there was protection from substitution masking.     

New objects,not new features,trigger the attentional blink

When two different targets must be selected from a rapid serial visual presentation (RSVP) of images, perception of the second target will be markedly reduced if it is presented within about a half second of the first. Known as the attentional blink (AB), this effect reflects temporal limitations in attentional processes enabling awareness of image representations. I tested whether these limitations occur at an object or feature level of processing by presenting (in RSVP) multiple images of the same (old) object depicted in different orientations. Targets were defined by new features added either to this or to a new object. When the first target feature appeared on the old object, no AB effects were found even when the second target was a new object. When a new object carried the first target feature, an AB effect was found even when the second target feature appeared on the same "new" object. The AB appears to reflect limitations in the creation of new object representations, rather than temporal limitations of awareness per se.     

Neural correlates of dual task interference in rapid visual streams: an fMRI study

In rapid streams of visual stimuli, identification of a first target interferes with identification of a second target presented within the next half second (the attentional blink or AB). It has been suggested that rapid perceptual decisions under masking interference involve interactions between frontal and posterior cortex. We investigated the neural correlates of the AB using functional magnetic resonance imaging (fMRI). Twelve subjects viewed rapid streams of black letters in which were embedded two white target letters (T1 and T2) separated by either 300 or 700 ms. As expected, fewer correct T2 identifications were observed in the short-delay condition. Corresponding fMRI statistical images showed increased activation in inferotemporal and posterior parietal cortex, but also in lateral frontal cortex and cerebellum in the short-delay condition suggesting that these brain regions are associated with perceptual decisions under masking interference.     

The roles of location specificity and masking mechanisms in the attentional blink

In a series of four experiments using rapid serial visual presentations of two target letters embedded in numeral distractors, with different numbers of display positions and with or without masking, we show that (1) the nonmonotonic, U-shaped attentional blink (AB) function, which occurs when all items are presented at the same display location, is eliminated in favor of a monotonic function when targets and distractors are presented randomly dispersed over four or nine adjacent positions; (2) the AB monotonicity is maintained with the spatially distributed presentation even when backward masks are used in all possible stimulus positions and when the location of the next item in sequence is predictable; and (3) the If-shaped AB is not due to position-specific forward or backward masking effects occurring at early levels of visual processing. We tentatively conclude that the U-shaped AB is primarily a function of the interruption of late visual processing produced when the item following the first target occurs at the same location. In order for the AB to severely disrupt performance, the item following the first target must be presented at the same location as the target so that it can serve both as a distractor and as a mask interrupting or interfering with subsequent visual processing.     

The roles of location specificity and masking mechanisms in the attentional blink.

In a series of four experiments using rapid serial visual presentations of two target letters embedded in numeral distractors, with different numbers of display positions and with or without masking, we show that (1) the nonmonotonic, U-shaped attentional blink (AB) function, which occurs when all items are presented at the same display location, is eliminated in favor of a monotonic function when targets and distractors are presented randomly dispersed over four or nine adjacent positions; (2) the AB monotonicity is maintained with the spatially distributed presentation even when backward masks are used in all possible stimulus positions and when the location of the next item in sequence is predictable; and (3) the U-shaped AB is not due to position-specific forward or backward masking effects occurring at early levels of visual processing. We tentatively conclude that the U-shaped AB is primarily a function of the interruption of late visual processing produced when the item following the first target occurs at the same location. In order for the AB to severely disrupt performance, the item following the first target must be presented at the same location as the target so that it can serve both as a distractor and as a mask interrupting of interfering with subsequent visual processing.     

The crossmodal facilitation of visual object representations by sound: evidence from the backward masking paradigm

We report a series of experiments designed to demonstrate that the presentation of a sound can facilitate the identification of a concomitantly presented visual target letter in the backward masking paradigm. Two visual letters, serving as the target and its mask, were presented successively at various interstimulus intervals (ISIs). The results demonstrate that the crossmodal facilitation of participants' visual identification performance elicited by the presentation of a simultaneous sound occurs over a very narrow range of ISIs. This critical time-window lies just beyond the interval needed for participants to differentiate the target and mask as constituting two distinct perceptual events (Experiment 1) and can be dissociated from any facilitation elicited by making the visual target physically brighter (Experiment 2). When the sound is presented at the same time as the mask, a facilitatory, rather than an inhibitory effect on visual target identification performance is still observed (Experiment 3). We further demonstrate that the crossmodal facilitation of the visual target by the sound depends on the establishment of a reliable temporally coincident relationship between the two stimuli (Experiment 4); however, by contrast, spatial coincidence is not necessary (Experiment 5). We suggest that when visual and auditory stimuli are always presented synchronously, a better-consolidated object representation is likely to be constructed (than that resulting from unimodal visual stimulation).