Involuntary attentional shifts due to orientation differences

We tested the ability of orientation differences to cause involuntary shifts of visual attention and found that these attentional shifts can occur in response to an orientation “pop-out” display. Texturelike cue stimuli consisting of discrete oriented bars, with either uniform orientation or containing a noninformative orthogonally oriented bar, were presented for a variable duration. Subsequent to or partially coincident with the cue stimulus was the target display of a localization or two-interval forced-choice task, followed by a mask display. Naive subjects consistently showed greater accuracy in trials with the target at the location of the orthogonal orientation compared with trials with uniformly oriented bars, with only 100 msec between the cue and mask onsets. Discriminating these orientations required a stimulus onset asynchrony (SOA) of 50–70 msec. The attentional facilitation is transient, in most cases absent, with a cue-mask SOA of 250 msec. These results suggest that the preattentive character of some texture discrimination tasks with SOAs of only 100 msec is vitiated by the involuntary attentional shifts that are caused by orientation differences.     

Facultative and inhibitory effects of location and frequency cues: Evidence of a modulation in perceptual sensitivity

The possibility that facilitative and inhibitory effects of auditory cues result because of a modulation in perceptual sensitivity was examined. Listeners were presented with a cue followed by a target, with the time period between the two varied at stimulus onset asynchronies (SOAs) of 150,450, or 750 msec. In two conditions, the cue and target were either the same or different in location or frequency. In both conditions, listeners were required to identify the rise time of the target. Whereas the cue was presented in isolation, the target was presented in a wide-band noise background such that the required discrimination was made relatively difficult. In both conditions, a facilitative effect was apparent at the 150-msec SOA and an inhibitory effect was apparent at the 750-msec SOA for both accuracy and response time measures of performance. That these results were apparent for a judgment unrelated to the manipulated cue-target relation suggests strongly that both location-based and frequency-based auditory inhibition of return result primarily because of changes in perceptual sensitivity.     

Facilitative and inhibitory effects of location and frequency cues: evidence of a modulation in perceptual sensitivity.

The possibility that facilitative and inhibitory effects of auditory cues result because of a modulation in perceptual sensitivity was examined. Listeners were presented with a cue followed by a target, with the time period between the two varied at stimulus onset asynchronies (SOAs) of 150, 450, or 750 msec. In two conditions, the cue and target were either the same or different in location or frequency. In both conditions, listeners were required to identify the rise time of the target. Whereas the cue was presented in isolation, the target was presented in a wide-band noise background such that the required discrimination was made relatively difficult. In both conditions, a facilitative effect was apparent at the 150-msec SOA and an inhibitory effect was apparent at the 750-msec SOA for both accuracy and response time measures of performance. That these results were apparent for a judgment unrelated to the manipulated cue-target relation suggests strongly that both location-based and frequency-based auditory inhibition of return result primarily because of changes in perceptual sensitivity.     

Preparation for horizontal or vertical dimensions affects the right-left prevalence effect

When stimulus and response simultaneously vary in both horizontal and vertical dimensions, the stimulus-response compatibility effect is often larger for the horizontal dimension. We investigated the role of preparation for each dimension in this right-left prevalence. In Experiment 1, tasks based on horizontal and vertical dimensions were mixed in random order, and the relevant dimension in each trial was cued with a variable cue-target stimulus onset asynchrony (SOA). A right-left prevalence effect was observed only when participants prepared for the upcoming task. Experiment 2 replicated the absence of the prevalence effect for the simultaneous presentation of cue and target using a fixed SOA of 0 msec. In Experiment 3, the right-left prevalence emerged with a 0-msec SOA when participants prepared for e achdimension basedon its frequency. These resultssuggest that participants' internal set can be greater for the horizontal dimension, leading to the right-left prevalence effect.     

Inhibition and decay of motor and nonmotor priming

Motor responses can be facilitated by congruent visual stimuli and prolonged by incongruent visual stimuli that are made invisible by masking (direct motor priming). Recent studies on direct motor priming showed a reversal of these priming effects when a three-stimulus paradigm was used in which a prime was followed by a mask and a target stimulus was presented after a delay. A similar three-stimulus paradigm on nonmotor priming, however, showed no reversal of priming effects when the mask was used as a cue for processing of the following target stimulus (cue priming). Experiment 1 showed that the time interval between mask and target is crucial for the reversal of priming. Therefore, the time interval between mask and target was varied in three experiments to see whether cue priming is also subject to inhibition at a certain time interval. Cues indicated (1) the stimulus modality of the target stimulus, (2) the task to be performed on a multidimensional auditory stimulus, or (3) part of the motor response. Whereas direct motor priming showed the reversal of priming about 100 msec after mask presentation, cue priming effects simply decayed during the 300 msec after mask presentation. These findings provide boundary conditions for accounts of inverse priming effects.     

Perception without awareness: further evidence from a Stroop priming task

In the present research, we examined the influence of prime-target stimulus onset asynchrony (SOA) on Stroop-priming effects from masked words. Participants indicated the color of a central target, which was preceded by a 33-msec prime word followed either immediately or after a variable delay by a pattern mask. The prime word was incongruent or congruent with the target color on 75% and 25% of the trials, respectively. The words followed by an immediate mask produced reliable Stroop interference at SOAs of 300 and 400 msec but not at SOAs of 500 and 700 msec. The words followed by a delayed mask produced a reversed (i.e., facilitatory) Stroop effect, which reached significance at an SOA of 400 msec or longer, but never at the shorter 300-msec SOA. Such an differential time course of both types of Stroop priming effects provides further evidence for the existence of qualitative differences between conscious and nonconscious perceptual processes.     

Time course of chord priming

The time course of chord priming was explored in four experiments. In chord priming, a chord (a typical combination of simultaneously sounded tones) primes other chords that are musically related. In the present study, the prime duration and the stimulus onset asynchrony (SOA) between the prime chord and the chord to be judged were varied. Priming occurred at an SOA and prime duration as short as 50 msec, the shortest tested. When the prime duration was held constant at 50 msec, priming occurred at an SOA as long as 2,500 msec, the longest tested, and the magnitude of the priming effect did not diminish. To eliminate a possible role of sensory memory in maintaining the priming effect during the silence following the prime, a 250-msec noise mask was presented immediately following the 50-msec prime. The interpolated noise mask did not eliminate priming, thereby supporting the view that chord priming is the consequence of associative activation.     

Time course of chord priming.

The time course of chord priming was explored in four experiments. In chord priming, a chord (a typical combination of simultaneously sounded tones) primes other chords that are musically related. In the present study, the prime duration and the stimulus onset asynchrony (SOA) between the prime chord and the chord to be judged were varied. Priming occurred at an SOA and prime duration as short as 50 msec, the shortest tested. When the prime duration was held constant at 50 msec, priming occurred at an SOA as long as 2,500 msec, the longest tested, and the magnitude of the priming effect did not diminish. To eliminate a possible role of sensory memory in maintaining the priming effect during the silence following the prime, a 250-msec noise mask was presented immediately following the 50-msec prime. The interpolated noise mask did not eliminate priming, thereby supporting the view that chord priming is the consequence of associative activation.     

Variation in cue duration reveals top-down modulation of involuntary orienting to uninformative symbolic cues

This article reports three experiments in which the effects of cue duration on involuntary orienting to uninformative symbolic cues (arrows presented at fixation) were investigated. Experiment 1 showed that symbolic cues had less effect on involuntary orienting when they were presented for only 25 msec than when they were presented for 200 msec across a range of stimulus onset asynchronies. Experiment 2 suggested that the effect of cue duration on involuntary orienting was due primarily to top-down strategic factors, rather than to bottom-up stimulus factors, and Experiment 3 suggested that these strategic factors may involve differences in how the cue is processed. Altogether, the present findings are important because they emphasize the distinction between cue processing and the putative involuntary orienting that results from such processing in the symbolic-cuing paradigm. In so doing, the present results help resolve discrepant findings that have been reported across previous studies.     

Metacontrast and brightness discrimination

An attempt was made to obtain U-shaped masking functions in two metacontrast experiments. Trained Ss judged whether a square test stimulus (TS) was bright or dim. The TS was presented alone or in conjunction with an adjacent pair of square masking stimuli (MS) whose energy equaled the bright TS. The stimulus onset asynchronies (SOA) rangedfrom 0 to 125 msec. The task minimized the role of apparent movement cues as a reliable basis for judgrnent. Similar studies have employed TS plus MS vs MS alone as the alternatives, allowing apparent movement to be a cue. Brightness accuracy was a U-shaped function of SOA. This finding is consistent with neural-net models (Weisstein, 1968). However, analysis of Ss’ response bias suggested an alternative explanation involving the MS as a comparison stimulus at short SOA. It was concluded that U-shaped masking functions are also consistent with theories based upon independent component processes, e.g., Schurman and Eriksen (1970) and Uttal (1970).     

Look away! Eyes and arrows engage oculomotor responses automatically

The present study investigates how people’s voluntary saccades are influenced by where another person is looking, even when this is counterpredictive of the intended saccade direction. The color of a fixation point instructed participants to make saccades either to the left or right. These saccade directions were either congruent or incongruent with the eye gaze of a centrally presented schematic face. Participants were asked to ignore the eyes, which were congruent only 20% of the time. At short gaze—fixation-cue stimulus onset asynchronies (SOAs; 0 and 100 msec), participants made more directional errors on incongruent than on congruent trials. At a longer SOA (900 msec), the pattern tended to reverse. We demonstrate that a perceived eye gaze results in an automatic saccade following the gaze and that the gaze cue cannot be ignored, even when attending to it is detrimental to the task. Similar results were found for centrally presented arrow cues, suggesting that this interference is not unique to gazes.     

Semantic activation in the absence of perceptual awareness

Participants performed a semantic categorization task on a target that was preceded by a prime word belonging either to the same category (20% of trials) or to a different category (80% of trials). The prime was presented for 33 msec and followed either immediately or after a delay by a pattern mask. With the immediate mask, reaction times (RTs) were shorter on related than on unrelated trials. This facilitatory priming reached significance at prime-target stimulus onset asynchronies (SOAs) of 400 msec or less and remained unaffected by task practice. With the delayed mask, RTs were longer on related than on unrelated trials. This reversed (strategic) semantic priming proved to be significant (1) only at a prime-target SOA of 400 msec or longer and (2) after the participants had some practice with the task. The present findings provide further evidence that perceiving a stimulus with and without phenomenological awareness can lead to qualitatively different behavioral consequences.     

Inhibition of return and attentional control settings

In the present study, we used a spatial cuing paradigm in conjunction with a choice identification task to investigate whether exogenous attentional orienting and inhibition of return are affected by attentional control settings. As in previous studies (e.g., Folk, Remington, & Johnston, 1992), onset- and color-defined targets were crossed with uninformative onset- and color-defined cues. As expected, when the cue-target stimulus onset asynchrony (SOA) was short (i.e., 100 msec), the results showed that exogenous attentional orienting was contingent on attentional set; attentional capture occurred in response to a particular cue only when the feature that defined the cue also defined the target (Folk et al., 1992). More importantly, when the cue-target SOA was long (i.e., 1,000 msec), the results showed that the occurrence of inhibition of return was also contingent on attentional set, at least partially so; inhibition of return occurred in response to onset cues only when they preceded onset targets. In contrast, inhibition of return never occurred in response to color cues (at a variety of long SOAs). The associations and dissociations that were observed between exogenous attentional orienting and inhibition of return are discussed in terms of posterior and anterior attention networks in the brain (Posner & Petersen, 1990).     

Configurational effects on the enumeration of dots: Counting by groups

The processing time for quantifying numerosity of two-dimensional dot patterns was investigated as a function of both number of dots and relative proximity between dots. A cluster algorithm (CODE) was first developed as a formal model of how human subjects organize neighboring dots into groups. CODE-based predictions of grouping effects on number processing latencies were then tested with patterns consisting of n dots (range n = 13–23). The results largely confirmed CODE-based predictions and thereby indicated that large collections of dots are preferably counted by groups. Small (n ≤ 5) groups are subitized and their partial results are summed to a running total. Based on criteria other than dot proximity, large (n > 5), proximity-based groups are subdivided into smaller groups of two or three dots, which are again subitized.     

跨通道语义启动对视觉注意的影响

采用生活中的真实客体,我们考察了跨通道语义相关性对视觉注意的影响以及跨通道促进的时程。结合启动范式和点探测范式,实验1发现在听觉启动600毫秒后,被试对高相关视觉刺激的反应比对低相关刺激的反应更快,而在视觉启动下没有发现启动效应。实验2发现在启动刺激呈现900毫秒后跨通道启动效应消失。我们的研究证明了基于先前经验的视、听语义相关能够促进视觉的选择性注意。     

Span of attention,backward masking,and reaction time

A test pattern consisting of 0 to 15 dots and a following random dot masking pattern were presented for 5 msec each with SOAs varying between 30 and 200 msec. The subject was asked to report the perceived number of dots in the test pattern as soon as possible and to assign a confidence rating to each report. The span of attention (upper limit for 50% correct numerosity judgments) increased from 2.4 to 9.5 as the SOA increased. Backward masking reduced the reported number of dots from the actual number in the test pattern, especially with small SOAs. Reaction time increased linearly at a low rate (approximately 40 msec/dot) up to 4 dots in the test pattern and then increased linearly at a high rate (approximately 370 msec/dot) as thereported, orperceived, number of dots increased. The two different branches of the reaction time curve were considered to represent two separate processes,subitizing andcounting, as suggested by Klahr (1973), who found similar dual increase rates as a function of the actual number of dots. These findings, as well as causal inference based on partial correlations and path analysis, indicated that the reported (perceived) number of dots and confidence rating were both determined by the number of stimulus dots and the SOA and that the reaction time was determined by the so-determined perceived number of dots and level of confidence. A multistage model is proposed.     

The role of temporal and spatial factors in the covert orienting of visual attention tasks

There is a biphasic pattern in response times to peripheral uninformative cues, with faster responses to targets in cued locations when the stimulus onset asynchrony (SOA) is under 300 ms and slower responses when it is over 300 ms. The effect has typically been attributed entirely to the SOA while ignoring other aspects of the cues (duration, spatial configuration). To examine these other factors, along with SOA, the present experiments included manipulations of SOA (50, 100, 200, 400, 800 ms), inter-stimulus interval (ISI; 0, 50, 100, 150, 200, 300, 350, 400, 500, 600, 700, and 750 ms), and whether or not the cue and target overlap in the same space. The results indicate that cueing effects depend on the combination of cue duration, ISI, SOA, and the spatial configuration of the cues and targets. Three factors are used to explain these time course results.     

Retrospective perceptual distortion of position representation does not lead to delayed localization

Previous studies have reported retrospective influences of visual events that occur after target events. In the attentional attraction effect, a position cue presented after a target stimulus distorts the target’s position towards that of the cue. The present study explored the temporal relationship between stimulus presentation and reaction time (RT) in this effect in two experiments. Participants performed a speeded localization task on two vertical lines, the positions of which were to be distorted by an additional attentional cue. No significant difference in RTs was found between the conditions with simultaneous and delayed cues. RTRT was modulated by the perceived (rather than physical) alignment of the lines. In Experiment 2, we manipulated the strength of attentional capture by modulating the color relevance of the cue to the target. Trials with cues producing stronger attentional capture (with cues of a different color from the targets) were found to induce apparently stronger distortion effects. This result favors the notion that the observed repulsion and attraction effects are driven by attentional mechanisms. Overall, the results imply that the attentional shift induced by the cue might occur rapidly and complete before the establishment of conscious location representation of the cue and the target without affecting overall response time.     

On the relation between auditory spatial attention and auditory perceptual asymmetries.

Laterality investigators have typically interpreted any perceptual asymmetry as a direct expression of the functional organization of the brain. However, many other confounding factors, including the asymmetric distribution of attention, may also contribute to either the magnitude or the direction of any of these advantages. In two experiments, attention was manipulated in a dichotic listening paradigm by presenting a preexposural tone cue to the ear from which the subject was required to report. The time available to orient attention was manipulated by varying the time period between the onset of the cue and the onset of the trial (stimulus onset asynchrony, or SOA). Results indicated that a right ear advantage for the identification of verbal material obtained at a 150-msec SOA was almost completely eliminated at an SOA of 450 msec. In addition, the direction of the ear advantage for emotion identification was found to depend on task difficulty. A left ear advantage, apparent when task difficulty was minimal, was reversed to a right ear advantage when difficulty was increased. These data are taken as evidence that, when subjects are faced with a difficult dichotic task, there is a general tendency for right-handed subjects to bias their attention toward the right ear. Such a tendency is shown not only to have likely seriously compromised the results of past investigations of functional perceptual asymmetries but also to be inconsistent with previously proposed theories of dichotic listening performance.     

On the relation between auditory spatial attention and auditory perceptual asymmetries

Laterality investigators have typically interpreted any perceptual asymmetry as a direct expression of the functional organization of the brain. However, many other confounding factors, including the asymmetric distribution of attention, may also contribute to either the magnitude or the direction of any of these advantages. In two experiments, attention was manipulated in a dichotic listening paradigm by presenting a preexposural tone cue to the ear from which the subject was required to report. The time available to orient attention was manipulated by varying the time period between the onset of the cue and the onset of the trial (stimulus onset asynchrony, or SOA).Results indicated that a right ear advantage for the identification of verbal material obtained at a 150-msec SOA was almost completely eliminated at an SOA of 450 msec. In addition, the direction of the ear advantage for emotion identification was found to depend on task difficulty. A left ear advantage, apparent when task difficulty was minimal, was reversed to a right ear advantage when difficulty was increased. These data are taken as evidence that, when subjects are faced with a difficult dichotic task, there is a general tendency for right-handed subjects to bias their attention toward the right ear. Such a tendency is shown not only to have likely seriously compromised the results of past investigations of functional perceptual asymmetries but also to be inconsistent with previously proposed theories of dichotic listening performance.