Feature-based attention to unconscious shapes and colors

Two experiments employed feature-based attention to modulate the impact of completely masked primes on subsequent pointing responses. Participants processed a color cue to select a pair of possible pointing targets out of multiple targets on the basis of their color, and then pointed to the one of those two targets with a prespecified shape. All target pairs were preceded by prime pairs triggering either the correct or the opposite response. The time interval between cue and primes was varied to modulate the time course of feature-based attentional selection. In a second experiment, the roles of color and shape were switched. Pointing trajectories showed large priming effects that were amplified by feature-based attention, indicating that attention modulated the earliest phases of motor output. Priming effects as well as their attentional modulation occurred even though participants remained unable to identify the primes, indicating distinct processes underlying visual awareness, attention, and response control.     

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.     

Response-mediated spatial priming despite perfectly valid target location cues and intervening response events

Attentional effects are often inferred from keypress reaction time (RT) studies when two sequentially presented stimuli, appearing at the same location, generate costs or benefits. The universality of these attentional attributions is challenged by data from perceptual discrimination tasks, which reveal that location repetition benefits and costs depend on whether a prior response repeats or switches, respectively. According to dual-stage accounts, these post-attentional effects may be abolished by making responses in between two target stimuli or by increasing target location certainty, leaving only attentional effects. Here, we test these accounts by requiring responses to stimuli in between targets and by increasing target location certainty with 100% valid location cues. Contrary to expectations, there was no discernible effect of cueing on any repetition effects, although the intervening response diminished stimulus-response repetition effects while subtly reducing location-response repetition effects. Despite this, there was little unambiguous evidence of attentional effects independent of responding. Taken together, the results further highlight the robustness of location-response repetition effects in perceptual discrimination tasks, which challenge whether there are enduring attentional effects in this paradigm.     

The manifestation of attentional capture: facilitation or IOR depending on task demands

Orienting attention exogenously to a location can have two different consequences on processing subsequent stimuli appearing at that location: positive (facilitation) at short intervals and negative (inhibition of return) at long ones. In the present experiments, we manipulated the frequency of targets and responses associated with them. Results showed that, even at long SOAs, where IOR is usually observed, facilitation was observed for infrequent targets at the same time that IOR was measured for frequent targets. These results are difficult to explain on the basis of either task set modulation of attentional capture or task set modulation of subsequent orienting processes. In contrast, we offer an explanation by which the different cuing effects can be considered as different manifestations of attentional capture on target processing, depending on the task set.     

Investigating the time course of tactile reflexive attention using a non-spatial discrimination task

Peripheral cues are thought to facilitate responses to stimuli presented at the same location because they lead to exogenous attention shifts. Facilitation has been observed in numerous studies of visual and auditory attention, but there have been only four demonstrations of tactile facilitation, all in studies with potential confounds. Three studies used a spatial (finger versus thumb) discrimination task, where the cue could have provided a spatial framework that might have assisted the discrimination of subsequent targets presented on the same side as the cue. The final study circumvented this problem by using a non-spatial discrimination; however, the cues were informative and interspersed with visual cues which may have affected the attentional effects observed. In the current study, therefore, we used a non-spatial tactile frequency discrimination task following a non-informative tactile white noise cue. When the target was presented 150 ms after the cue, we observed faster discrimination responses to targets presented on the same side compared to the opposite side as the cue; by 1000 ms, responses were significantly faster to targets presented on the opposite side to the cue. Thus, we demonstrated that tactile attentional facilitation can be observed in a non-spatial discrimination task, under unimodal conditions and with entirely non-predictive cues. Furthermore, we provide the first demonstration of significant tactile facilitation and tactile inhibition of return within a single experiment.     

Modulating the attentional repulsion effect

The attentional repulsion effect refers to the perceived displacement of a visual stimulus in a direction that is opposite to a brief peripheral cue. If the spatial repulsion brought about by peripheral cues is in fact attentional in nature, then attentional manipulations that produce known effects on reaction time should have analogous spatial repulsions effects. Across three experiments, we show that the attentional repulsion effect does indeed mimic results obtained from temporal (i.e., reaction time) attentional tasks, including single onset, offset and onset-offset cue displays (Experiment 1), simultaneous onset and offset displays (Experiment 2), and pop-out color displays (Experiment 3). Thus, the attentional repulsion effect can be modulated by attentional manipulations. Moreover, it appears that attentional processes underlying changes related to when targets are perceived appear to be the same as those underlying changes related to perceiving where targets are.     

Spatial probability as an attentional cue in visual search

We investigated the role of spatial probabilities in target location during participants' performance of a visual search task. Experiments 1 and 2 demonstrated that spatial probabilities could serve as a powerful attentional bias that produced faster detection of targets in high-probability locations than of those in low- or random-probability locations. The effect could not be explained by repetition priming alone. Moreover, responses to targets in low-probability locations were slowed only when a distractor was present in the high-probability location. In Experiments 3-5, we compared the effects of spatial probability with an explicit endogenous cue and a salient exogenous cue. Facilitation due to spatial probability was independent of any benefit afforded by the explicit endogenous cue but interacted with the salient exogenous cue, such that the exogenous cue validity effect was compressed for targets in the high-probability location. Together, these results suggest that the spatial probabilities governing target location constitute a potent bias of visual processing and, as such, can be considered an attentional cue that differs from both typical explicit endogenous and salient exogenous cues.     

The effects of onsets and offsets on visual attention

 Two experiments are presented which examine the effect of onset and offset cues on early occurring attentional cueing effects and later occurring inhibition of return (IOR). The first experiment compared the effects of single onset cues, single offset cues, and simultaneous onset and offset cues (at opposite locations) at a 100-ms stimulus-onset-asynchrony (SOA) and IOR at a 900-ms SOA. Whereas the first experiment examined these conditions with choice localization keypress responses, the second experiment used simple detection keypress responses. Both experiments found that onset and offset cues presented in isolation produce early facilitation and late IOR. When onset and offset cues were simultaneously presented, facilitation but not IOR was found with localization responses, while neither facilitation or IOR was found with detection responses. Overall, these findings suggest that offset cues can be treated in the same manner as onset cues by the attentional system, although the onset cues may have priority in orienting attention when targets must be localized in space. Received: 26 May 2000 / Accepted: 31 January 2001     

Allocation of visual attention in younger and older adults.

Younger and older adults were compared in three experiments, using procedures that had been shown to affect the spread of visual attention. The attentional effects found in previous experiments were replicated. A broader focus of attention speeded responses to peripheral targets. In addition, two established findings concerning aging were replicated: Responses were slower in older than in younger adults, and, in certain conditions, they slowed more rapidly as target eccentricity increased. No interactions of age effects with attentional manipulations were found. The results of all three experiments were consistent with the interpretation that younger and older adults do not differ in the allocation of attention.     

Effects of alcohol on person perception: a social cognitive neuroscience approach

The acute effects of alcohol on cognitive processing of expectancy violations were investigated using event-related brain potentials and a cued recall task to index attentional and working memory processes associated with inconsistency resolution. As predicted, expectancy-violating behaviors elicited larger late positive potentials (LPP) and were recalled better than expectancy-consistent behaviors. These effects were moderated by alcohol and the valence of initial expectancies. For placebo group participants, positive targets performing negative behaviors elicited the largest LPP responses and were recalled best. For those in the alcohol groups, negative targets behaving positively elicited the largest LPP and recall responses. These findings suggest that alcohol does not globally impair working memory processes in person perception but instead changes the nature of valenced information processing. Findings are discussed in the context of alcohol's effects on working memory processes, reward sensitivity, and the prefrontal cortical structures thought to mediate them.     

Visual attention amplifies response priming of pointing movements to color targets

We studied the influence of spatial visual attention on the time course of primed pointing movements. We measured pointing responses to color targets preceded by color stimuli priming either the same response as the target or the opposite response. The effects of visual attention at the prime and target locations were studied by varying both the cue-prime and prime-target intervals when presenting either exogenous attentional cues or, in a separate experiment, endogenous cues whose processing was a precondition for performing the task. Pointing trajectories revealed large priming effects in which pointing responses were first controlled by prime signals and then captured in midflight by target signals. Priming effects were strongly amplified when the relevant prime locations were visually attended at optimal cue-prime SOAs, with attention modulating the entire time course of the primed pointing movements. We propose that visual attention amplifies the earliest waves of visuomotor feedforward information, elicited in turn by primes and by targets.     

Allocation of visual attention in younger and older adults

Younger and older adults were compared in three experiments, using procedures that had been shown to affect the spread of visual attention. The attentional effects found in previous experiments were replicated. A broader focus of attention speeded responses to peripheral targets. In addition, two established findings concerning aging were replicated: Responses were slower in older than in younger adults, and, in certain conditions, they slowed more rapidly as target eccentricity increased. No interactions of age effects with attentional manipulations were found. The results of all three experiments were consistent with the interpretation that younger and older adults do not differ in the allocation of attention.     

Top-down search strategies determine attentional capture in visual search: Behavioral and electrophysiological evidence

To investigate how attentional capture in visual search is affected by generalized top-down search strategies, ERPs and behavioral performance were measured in two experiments where spatially nonpredictive color singleton cues preceded visual search arrays that contained one of two equally likely color singletons. When both singletons served as targets, irrelevant-color singleton cues produced behavioral attentional capture effects and elicited an N2pc component, indicative of a singleton search mode. When responses were required to only one of the two color singletons, the same cues no longer elicited behavioral spatial cuing effects, and the N2pc to these cues was attenuated and delayed, in line with the hypothesis that search was now guided by a feature-specific search strategy. Results demonstrate that the ability of visual singleton stimuli to capture attention is not simply determined by their bottom-up salience, but strongly modulated by top-down task sets.     

The adaptive character of the attentional system: statistical sensitivity in a target localization task

A localization task required participants to indicate which of 4 locations contained a briefly displayed target. Most displays also contained a distractor that was not equally probable in these locations, affecting performance dramatically. Responses were faster when a display had no distractor and almost as fast when the distractor was in its frequent location. Conversely, responses were slower when targets appeared in frequent-distractor locations, even thou targets were equally likely in each location. Negative-priming effects were reliably smaller when targets followed distractors in the frequent-distractor location compared to the rare-distractor location, challenging the episodic-retrieval account Experiment 2 added a 5th location that rarely displayed distractors and never targets, yet responses slowed most when distractors appeared there. The results confirmed that the attentional system is sensitive to first- and higher-order statistical patterns and can make short- and long-term adjustments in preferences based on prior history of inspecting unsuccessful locations.     

The role of attentional set on attentional cueing and inhibition of return

When people know what critical feature will define a target for a block of trials, only cues that share a critical feature with targets will capture attention. This result is taken to mean that attentional control settings play a role in target identification. To examine the validity of the attentional control settings hypothesis while controlling for potential sensory artifacts, the first experiment compared conditions in which the critical target features were either blocked or randomized. The results indicated that all cues captured attention in the random conditions, but only cues that matched targets captured attention in the attentional set condition. The second experiment used the same two conditions to examine the effect of attentional set on inhibition of return (IOR). No differences were found between the blocked and random conditions, indicating that attentional set did not impact the IOR effects. Overall, the results indicate that (1) the previous findings of attentional set effects were not due to an artifact of the method, and (2) attentional set influences and early occurring attentional cueing effects but not later-occurring IOR effects.     

Masked singleton effects

In the present study, we tested whether visual singletons remaining outside awareness are processed. Singletons differ by at least one feature from their more homogeneous neighbors. Here, we used backward masking to prevent awareness of shape singleton primes (Experiments 1-4) or color singleton primes (Experiment 5). Masked singleton primes nonetheless produced a congruence effect: Congruent singletons indicating the location of subsequent visible targets facilitated responses, in comparison with incongruent singletons at positions away from the targets. This congruence effect was found with singletons defined by feature presence or feature absence. It was at least partly due to attentional capture by singletons remaining outside of the participants' awareness. Results are discussed in light of theories pertaining to singleton effects and masked-priming effects.     

Target—distractor interference in the attentional blink implicates the locus coeruleus—norepinephrine system

We provide evidence that the locus coeruleus—norephinephrine (LC-NE) system is the neurophysiological basis of the attentional blink. The attentional blink refers to decreased accuracy for reporting the second of two targets in a rapid serial visual presentation of distractors. The LC-NE account of the attentional blink posits that targets elicit a facilitative LC-NE system response that is available for the first target but subsequently unavailable to the second, due to the autoinhibitory nature of the LC-NE system. We propose a modification of the LC-NE account, suggesting that the LC-NE system response is elicited by interference between mutually exclusive responses demanded by temporally proximal targets and distractors. We increased the interference between the first target and the following distractor by reducing the time between them. For identifying the second target this high-interference condition yielded a benefit up to 200 msec after onset of the first, followed by a decrease in accuracy. Consistent with our modification of the LC-NE account, this result suggests a temporarily enhanced LC-NE system response to increased target—distractor interference.     

Traces left on visual selective attention by stimuli that are not consciously identified

Briefly presented information, even if unidentifiable, may speed or delay required responses to following events. It has been assumed that this priming of the motor system may occur without affecting attention to priming and following stimuli. In contrast to this notion, the present study reports that such unidentified stimuli have effects on a physiological indicator of the attentional system. A lateral posterior electroencephalogram component was evoked by laterally presented relevant shapes, reflecting shifts of attention to those shapes. This component was absent, however, when the relevant shape was preceded by a similar shape at the same location, even if this shape was completely masked by metacontrast. The attentional shift evidently became unnecessary in this situation. Thus, unidentifiable information may leave some trace for attention-controlled selection of the following event.     

Attentional bias towards angry faces is moderated by the activation of a social processing mode in the general population

ABSTRACT

Dot-probe studies usually find an attentional bias towards threatening stimuli only in anxious participants, but not in non-anxious participants. In the present study, we conducted two experiments to investigate whether attentional bias towards angry faces in unselected samples is moderated by the extent to which the current task requires social processing. In Experiment 1, participants performed a dot-probe task involving classification of either socially meaningful targets (schematic faces) or meaningless targets (scrambled schematic faces). Targets were preceded by two photographic face cues, one angry and one neutral. Angry face cues only produced significant cueing scores (i.e. faster target responses if the target replaced the angry face compared to the neutral face) with socially meaningful targets, not with meaningless targets. In Experiment 2, participants classified only meaningful targets, which were either socially meaningful (schematic faces) or not (schematic houses). Again, mean cueing scores were significantly moderated by the social character of the targets. However, cueing scores in this experiment were non-significant in the social target condition and significantly negative in the non-social target condition. These results suggest that attentional bias towards angry faces in the dot-probe task is moderated by the activation of a social processing mode in unselected samples.     

Attentional Orienting in Two-dimensional Space

This paper examines how the covert orienting of spatial attention affects motor responses to visual stimuli. Premotor theories, as well as hemi-field inhibition accounts of visual attention predict an increase in response times when a target stimulus appears in the opposite direction to a spatial cue. Some models also suggest that this meridional effect should be increased across oblique meridians. Two types of cue (central and peripheral) were used to orient attention towards locations prior to the onset of visual targets. Simple manual (press button) and saccadic responses were measured. No meridional effects were found with peripheral cues, whereas central cueing produced meridional effects across all meridians. Cueing effects did not vary significantly with two-dimensional axis for either manual or saccadic responses. Increases in response time with cue-target distance were found for both response and cue types. For saccades, distance gradients were shallower moving distally rather than proximally from the cued position. However, simple manual responses did not show this asymmetry. Orienting to central cues also modulated the amplitude of saccades. The results are consistent with an effect of attentional cues in oculomotor centres as well as the existence of actiondependent attentional representations. However, it is proposed that, rather than reflecting oculomotor programming, meridional effects arise from a directional organization within spatio-cognitive representations.