Role of task-directed attention in nonconscious and conscious response priming by form and color.

Prior research on visual priming suggests that during nonconscious processing attention can be directed to single stimulus dimensions such as form or color. In the current experiment, nonconscious priming was compared to conscious priming by employing masking techniques that render primes invisible (masked) or visible (unmasked) to the observers. Observers were asked to respond to the form, the color, or the combination of form and color of the mask-probe that followed either a masked or an unmasked prime. The prime varied in its form and color congruency relative to the mask-probe. The results indicate (1) that during nonconscious processing a task-irrelevant stimulus feature can be attentionally filtered out, (2) that during nonconscious processing only separated stimulus features can be attended, and (3) that during conscious processing the conjunction of stimulus features comprising an object can be attended. Furthermore, the results indicate that at the nonconscious level stimuli are processed at an individual-feature level, while at the conscious level the stimuli can additionally be processed at a whole-object level. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Luminance and spatial attention effects on early visual processing

Event-related potentials (ERPs) were recorded from healthy subjects in response to unilaterally flashed high and low luminance bar stimuli presented randomly to left and right field locations. Their task was to covertly and selectively attend to either the left or right stimulus locations (separate blocks) in order to detect infrequent shorter target bars of either luminance. Independent of attention, higher stimulus luminance resulted in higher ERP amplitudes for the posterior N95 (80-110 ms), occipital P1 (110-140 ms), and parietal N1 (130-180 ms). Brighter stimuli also resulted in shorter peak latency for the occipital N1 component (135-220 ms); this effect was not observed for the N1 components over parietal, central or frontal regions. Significant attention-related amplitude modulations were obtained for the occipital P1, occipital, parietal and central N1, the occipital and parietal P2, and the parietal N2 components; these components were larger to stimuli at the attended location. In contrast to the relatively short latencies of both spatial attention and luminance effects, the first interaction between luminance and spatial attention effects was observed for the P3 component to the target stimuli (350-750 ms). This suggests that interactions of spatial attention and stimulus luminance previously reported for reaction time measures may not reflect the earliest stages of sensory/perceptual processing. Differences in the way in which luminance and attention affected the occipital P1, occipital N1 and parietal N1 components suggest dissociations among these ERPs in the mechanisms of visual and attentional processing they reflect.(ABSTRACT TRUNCATED AT 250 WORDS)     

Spatio-temporal dynamics of attention to color: evidence from human electrophysiology

This study characterized patterns of brain electrical activity associated with selective attention to the color of a stimulus. Multichannel recordings of event-related potentials (ERPs) were obtained while subjects viewed randomized sequences of checkerboards consisting of isoluminant red or blue checks superimposed on a grey background. Stimuli were presented foveally at a rapid rate, and subjects were required to attend to the red or blue checks in separate blocks of trials and to press a button each time they detected a dimmer target stimulus of the attended color. An early negative ERP component with an onset latency of 50 ms was sensitive to stimulus color but was unaffected by the attentional manipulation. ERPs elicited by attended and unattended stimuli began to diverge after approximately 100 ms following stimulus onset. Inverse dipole modelling of the attended-minus-unattended difference waveform indicated that an initial positive deflection with an onset latency of 100 ms had a source in lateral occipital cortex, while a subsequent negative deflection with an onset at 160 ms had a source in inferior occipito-temporal cortex. Longer-latency attention-sensitive components were localized to premotor frontal areas (onset at 190 ms) and to more anterior regions of the fusiform gyrus (onset at 240 ms). These source localizations correspond closely with cortical areas that were identified in previous neuroimaging studies as being involved in color-selective processing. The present ERP data thus provide information about the time course of stimulus selection processes in cortical areas that subserve attention to color.     

Technologically enhanced naturally occurring radioactive material (NORM): pathway analysis and radiological impact

Event-related potentials were recorded from 80 participants ranging in age from 7 to 24 years while they attended selectively to stimuli with a specified color (red or blue) in an attempt to detect the occurrence of target stimuli. Color attention effects were identified as frontal selection positivity (FSP; 140-275 ms), selection negativity (SN; 150-300 ms), and N2b (200-450 ms), whereas target detection was reflected in P3b (300-700 ms). There were age-related decreases in the latencies of FSP, N2b, and P3b that paralleled decreases in reaction time and error rates. Also, the SN amplitude increased with advancing age, whereas both N2b and P3b showed changes in scalp topography. These results represent neurophysiological evidence that the efficiency of visual selective processes increases during childhood and adolescence. Developmental growth may take place at both relatively early and late levels of visual selective information processing.     

Effects of attention on infants' preference for briefly exposed visual stimuli in the paired-comparison recognition-memory paradigm.

This study examined the effect of attention on 3- to 6-mo-olds' responses to briefly exposed visual stimuli. In Study 1, stimuli presented at 2.5 or 5.0 s resulted in a familiarity preference in a subsequent paired-comparison procedure. A novelty preference was found with 10.0- or 20.0-s exposure durations. In Study 2, a Sesame Street movie elicited heart-rate-defined attention phases and stimuli replaced Sesame Street during sustained attention, attention termination, or 5.0 s following attention termination. For 20 and 26-wk-olds, stimuli presented for 5.0 s during sustained attention resulted in a novelty preference similar to that found when exposure time was 20.0 s. The duration of stimulus exposure during sustained attention in the familiarization phase was positively correlated with the preference for the novel stimulus in the paired-comparison procedure. Thus, processing of briefly presented visual stimuli differs depending on the type of attention in which the infant is currently engaged. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Interference from irrelevant features on visual discrimination by macaques (Macaca fuscata): A behavioral analogue of the human Stroop effect.

To study the operation of selective attention in a conflict situation with automatic processes, we trained 4 Japanese macaques; (Macaca fuscata) extensively on a manual go/no-go task. The monkey had to discriminate either the color, shape, motion direction, or location of a visual stimulus. In each trial, the behavioral meaning of the relevant feature (go or no-go) could either be congruent or incongruent with irrelevant features of the same stimulus. Reaction times were slowed, and error rates increased when irrelevant stimulus features were incongruent with the required response. The effects were obtained when the monkey attended to the color, shape, or motion direction, but not when it attended to the location of the stimulus. The effects were cumulative so that the interference from 1 incongruent feature was smaller than that from 2 incongruent features. We propose that the present paradigm provides a behavioral analogue of the human Stroop effect. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Visual attention mediated by biased competition in extrastriate visual cortex

According to conventional neurobiological accounts of visual attention, attention serves to enhance extrastriate neuronal responses to a stimulus at one spatial location in the visual field. However, recent results from recordings in extrastriate cortex of monkeys suggest that any enhancing effect of attention is best understood in the context of competitive interactions among neurons representing all of the stimuli present in the visual field. These interactions can be biased in favour of behaviourally relevant stimuli as a result of many different processes, both spatial and non-spatial, and both bottom-up and top-down. The resolution of this competition results in the suppression of the neuronal representations of behaviourally irrelevant stimuli in extrastriate cortex. A main source of top-down influence may derive from neuronal systems underlying working memory.     

Effects of inter- and intramodal selective attention to non-spatial visual stimuli: an event-related potential analysis

Event-related potentials (ERPs) were recorded to trains of rapidly presented auditory and visual stimuli. ERPs in conditions in which subjects attended to different features of visual stimuli were compared with ERPs to the same type of stimuli when subjects attended to different features of auditory stimuli. This design permitted us to study effects of variations in both intramodal and intermodal visual attention on the timing and topography of ERP components in the same experiment. There were no indications that exogenous N110, P140 and N180 components to line gratings of high and low spatial frequencies were modulated by either intra- or intermodal forms of attention. Furthermore, intramodal and intermodal attention effects on ERPs showed similar topographical distributions. These combined findings suggest that the same neural generators in extrastriate occipital areas are involved in both forms of attention. Visual ERPs elicited in the condition in which subjects were engaged in auditory selective attention showed a large positive displacement at the occipital scalp sites relative to ERPs to attended and unattended stimuli in the visual condition. The early onset of this positivity might be associated with a highly confident and early rejection of the irrelevant visual stimuli, when these stimuli are presented among auditory stimuli. In addition, the later onset of selection potentials in the intramodal condition suggests that a more precise stimulus selection is needed when features of visual stimuli are rejected among other features of the same stimulus pattern, than when visual stimuli are rejected among stimuli of another modality.     

4 T-fMRI study of nonspatial shifting of selective attention: cerebellar and parietal contributions

Regional blood oxygenation in the cerebellum and posterior cerebral cortices was monitored with functional magnetic resonance imaging (fMRI) at four Tesla while 16 normal subjects performed three tasks with identical visual stimulation: fixation; attention focused upon either stimulus shape or color and sustained during blocks of trials (sustained attention); and rapid, serial shifts in attention between stimulus shape or color within blocks of trials (shifting attention). The stimuli were displayed centrally for 100 ms followed by a central fixation mark for 900 ms. Each stimulus was either a circle or a square displayed in either red or green. Attention shifting required switching between color and shape information after each target detection and occurred on average once every three seconds. Subjects pressed a response key upon detecting the target; reaction time and response accuracy were recorded. Two protocols for T2*-weighted echo-planar imaging were optimized, one with a surface coil for the cerebellum alone and the other with a volume coil for imaging both cerebellum and posterior brain structures (parietal, occipital, and part of temporal cortices). Because fMRI of the cerebellum is particularly susceptible to cardiac and respiratory fluctuations, novel techniques were applied to isolate brain activation signals from physiological noise. Functional activation maps were generated for contrasts of 1) sustained attention to color minus fixation; 2) sustained attention to shape minus fixation; and 3) shifting attention minus sustained attention (to color and shape; i.e., summed across blocks of trials). Consistent with the ease of these tasks, subjects performed with >80% accuracy during both sustained attention and shifting attention. Analysis of variance did not show significant differences in false alarms or true hits across either attentional condition. A subgroup of subjects whose performance data were recorded during ten minutes of continuous practice did not show significant changes over time. Both contrasts between the conditions of sustained attention to color or to shape as compared with the fixation condition showed significant bilateral activation in occipital and inferior temporal regions (Brodmann areas 18, 19, and 37). The anterior medial cerebellum was also significantly activated ipsilateral to the finger used for responding. The principal comparison of interest, the contrast between the condition of shifting attention and the condition of sustained attention produced significant and reproducible activation: lateral cerebellar hemisphere (ansiform lobule: Crus I Anterior and Crus I Posterior; left Crus I Posterior); cerebellar folium; posterior superior parietal lobule (R and L); and cuneus and precuneus (R and L).     

Directed attention prolongs the perceived duration of a brief stimulus

Stelmach, Herdman, and McNeil (1994) suggested recently that the perceived duration for attended stimuli is shorter than that for unattended ones. In contrast, the attenuation hypothesis (Thomas & Weaver, 1975) suggests the reverse relation between directed attention and perceived duration. We conducted six experiments to test the validity of the two contradictory hypotheses. In all the experiments, attention was directed to one of two possible stimulus sources. Experiments 1 and 2 employed stimulus durations from 70 to 270 msec. A stimulus appeared in either the visual or the auditory modality. Stimuli in the attended modality were rated as longer than stimuli in the unattended modality. Experiment 3 replicated this finding using a different psychophysical procedure. Experiments 4-6 showed that the finding applies not only to stimuli from different sensory modalities but also to stimuli appearing at different locations within the visual field. The results of all six experiments support the assumption that directed attention prolongs the perceived duration of a stimulus.     

Optimizing sound features for cortical neurons

The brain's cerebral cortex decomposes visual images into information about oriented edges, direction and velocity information, and color. How does the cortex decompose perceived sounds? A reverse correlation technique demonstrates that neurons in the primary auditory cortex of the awake primate have complex patterns of sound-feature selectivity that indicate sensitivity to stimulus edges in frequency or in time, stimulus transitions in frequency or intensity, and feature conjunctions. This allows the creation of classes of stimuli matched to the processing characteristics of auditory cortical neurons. Stimuli designed for a particular neuron's preferred feature pattern can drive that neuron with higher sustained firing rates than have typically been recorded with simple stimuli. These data suggest that the cortex decomposes an auditory scene into component parts using a feature-processing system reminiscent of that used for the cortical decomposition of visual images.     

Parent-victim agreement in adolescent suicide research

It is known that transcranial magnetic stimulation (TMS) administered over the occipital pole suppresses recognition of visual objects. Our aim was to ascertain whether this suppression can be interpreted as a change in visual contrast threshold. Four subjects detected the orientation of an U-shaped hook flashed for 21 ms. Under control conditions, mean contrast threshold was found at 0.88 log units Weber contrast. Thresholds were raised if TMS was applied 40-200 ms after the visual stimulus. Maximum elevation was 1.67 log units under TMS at 120 ms stimulus onset asynchrony. This phenomenon can be interpreted as a reduction in signal-to-noise ratio of the visual stimuli by TMS, which can be compensated for by increasing the contrast of the stimuli.     

Is there a mutual relationship between opposite attentional biases underlying anxiety?

Current models that account for attentional processes in anxiety have proposed that high-trait anxious individuals are characterized by a hypervigilant-avoidant pattern of attentional biases to threat. We adopted a laboratory conditioning procedure to induce concomitant hypervigilance and avoidance to threat, emphasizing a putative relationship between lower-level reactive and upper-level controlled attentional mechanisms as the core account of attentional processes involved in the development and maintenance of anxiety. Eighty high- and low-trait anxious participants underwent Pavlovian conditioning to a human face. Eye tracking was used to monitor attentional changes to the conditioned stimulus (CS+) face and the neutral stimulus (CS?) face, presented at 200, 500, and 800 ms durations. The high-anxious participants developed the expected attentional bias toward the CS+ at 200 ms presentation time and attentional avoidance at 500 and 800 ms durations. Hypervigilance to aversive stimuli at 200 ms and later avoidance to the same stimuli at 500 and 800 ms were associated with higher levels of galvanic skin conductance to the CS+. The low-anxious individuals developed the opposite attentional pattern with an initial tendency to orient attention away from the aversive stimuli in the 200 ms condition and to orient attention toward aversive stimuli in the remaining time. The differential modulation between hypervigilance and avoidance elicited in the two groups by the conditioning procedure suggests that vulnerability to anxiety is characterized by a latent relationship between diverse attentional mechanisms. Within this relationship, hypervigilance and avoidance to threat operate at different stages of information processing suggesting fuzzy boundaries between early reactive and later-strategic processing of threat. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

Separating perceptual and decisional attention processes in the identification and categorization of integral-dimension stimuli.

Four observers performed matching, identification, and categorization with stimuli that varied along the integral dimensions: brightness and saturation. General recognition theory (F. G. Ashby & J. T. Townsend, 1986) was applied to quantify the separate influences of perceptual and decisional processes within and across tasks, with a focus on separating perceptual from decisional attention processes. Good accounts of the identification data were obtained from perceptual matching representation. This perceptual representation provided a good account of the categorization data, except when decisional selective attention to 1 stimulus dimension was required. Decisional selective attention reduced the attended-dimension perceptual variance relative to the unattended-dimension perceptual variance, with a larger reduction resulting when brightness, as opposed to saturation was attended. Implications for color vision research are discussed. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Visual processing levels revealed by response latencies to changes in different visual attributes

Visual latencies, and their variation with stimulus attributes, can provide information about the level in the visual system at which different attributes of the image are analysed, and decisions about them made. A change in the colour, structure or movement of a visual stimulus brings about a highly reproducible transient constriction of the pupil that probably depends on visual cortical mechanisms. We measured this transient response to changes in several attributes of visual stimuli, and also measured manual reaction times to the same stimulus changes. Through analysis of latencies, we hoped to establish whether changes in different stimulus attributes were processed by mechanisms at the same or different levels in the visual pathway. Pupil responses to a change in spatial structure or colour are almost identical, but both are ca. 40 ms slower than those to a change in light flux, which are thought to depend largely on subcortical pathways. Manual reaction times to a change in spatial structure or colour, or to the onset of coherent movement, differ reliably, and all are longer than the reaction time to a change in light flux. On average, observers take 184 ms to detect a change in light flux, 6 ms more to detect the onset of a grating, 30 ms more to detect a change in colour, and 37 ms more to detect the onset of coherent motion. The pattern of latency variation for pupil responses and reaction times suggests that the mechanisms that trigger the responses lie at different levels in cortex. Given our present knowledge of visual cortical organization, the long reaction time to the change in motion is surprising. The range of reaction times across different stimuli is consistent with decisions about the onset of a grating being made in V1 and decisions about the change in colour or change in motion being made in V4.     

Signals of threat do not capture, but prioritize, attention: A conditioning approach.

Research suggests that threatening information captures attention more rapidly than neutral information. However, in most studies threat stimuli differ perceptually from neutral stimuli and are instrumental to perform the task, leaving the question unanswered whether threat is sufficient to capture attention. In experiment 1, we designed a visual search task with stimuli of equal salience (colored circles) that have the potential to lead to efficient search (10 ms/item). In experiment 2, one of the colors (conditioned stimulus, CS+) was made threatening by means of fear conditioning. Participants responded to a target presented in one of the circles. Overall, the search was faster on congruent trials (where the target was presented in the CS+) than on baseline trials (where the CS + was absent). Furthermore, the search was slower on incongruent trials (where the target was presented in another color than the CS+) than on baseline trials. The search on congruent trials was affected by set size (90 ms/item), but to a lesser extent than on baseline trials (105 ms/item). We conclude that threat prioritizes, but does not capture attention. (PsycINFO Database Record (c) 2011 APA, all rights reserved)     

Is there feature-based attentional selection in visual search?

A new paradigm combines attentional cuing and rapid serial visual presentation to disentangle the effects of perceptual filtering and location selection. Observers search successive, superimposed arrays, in which feature values are alternated for a target numeral among letters. Two dimensions, size (small, large) and color (red, green) are tested. Selective attention to feature values is jointly manipulated by instructions, presentation probabilities, and payoffs. In Experiment 1, the attended feature provides temporal, not spatial, information; observers show no attentional costs or benefits in response accuracy. In Experiment 2, the attended feature indicates a unique location; observers show consistent attentional costs and benefits. Selective attention to a particular size or color does not cause perceptual exclusion or admission of items containing that feature; it acts by guiding search processes to spatial locations that contain the to-be-attended feature. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

The role of selective attention in the perception of multiple-element stimulus arrays.

To access the role of attention in visual processing, we have recorded single-unit activity from area V4 of visual cortex in macaque monkeys, and the results of these experiments provide a clear demonstration of the relationship between inter-stimulus competition and attention. Specifically, attended stimuli elicit larger responses than ignored stimuli, and these attention effects are increased when: a) the total number of distracting stimuli is increased; b) both attended and ignored stimuli are located inside the neuron's receptive field; and c) the attended and ignored stimuli are presented simultaneously rather than sequentially. We have also examined the role of inter-stimulus competition in human subjects by recording event-related potentials (ERPs), which are electrophysiological responses that can be recorded noninvasively from the scalp. In these experiments, we have found that the attention-sensitive N2pc wave is present when subjects focus attention onto target stimuli when they are surrounded by competing distractor stimuli, but is absent when the competition is eliminated (e.g. by removing the distractors). (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Infant visual attentiveness in relation to birth condition.

28 preterm infants tested at 40 wks conceptional age showed significantly longer periods of attention to 2-dimensional stimuli than did 28 full-term infants of the same conceptional age (Exp I). To determine whether attentiveness of the full-term infants was diminished by transient birth effects, visual attentiveness was measured in a group of 15 full-term infants in the 1st 2 days of life and 2 wks later (Exp II). There was no significant increase in attention over this period. Furthermore, data from 62 additional preterm infants showed that fixation times were not significantly related to length of postnatal experience (Exp III). The only attention measure relating to birth condition was a measure of initial responsiveness. Healthier infants showed slightly longer first fixations on the first exposure of the stimulus. Initial responsiveness to visual stimuli may represent infant attentiveness more accurately than sustained attention to unchanging 2-dimensional stimuli. (17 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Inhibition of return: Effects of attentional cuing on eye movement latencies.

Inhibition of return refers to a bias against attending to and/or detecting visual stimuli at recently attended locations. A total of 57 Ss participated in 5 experiments, in which Ss were slower to initiate eye movements to previously attended locations. Furthermore, there was more inhibition when a peripheral (exogenous) flash signaled the target, compared with when a central (endogenous) arrow cue was used as an imperative stimulus. That pattern suggests that some of the inhibition is due to processes involved in detecting visual stimuli, and some of the inhibition is related to the movement of the eye. Subsequent experiments showed that the eye-movement component of the inhibition is not object-centered and does not move if the previously attended object moves, although the stimulus-detection component is object-centered. Results have implications for visual attention in general and for the link between overt and covert orienting. (PsycINFO Database Record (c) 2010 APA, all rights reserved)