Implicit learning for probable changes in a visual change detection task

Previous research demonstrates that implicitly learned probability information can guide visual attention. We examined whether the probability of an object changing can be implicitly learned and then used to improve change detection performance. In a series of six experiments, participants completed 120–130 training change detection trials. In four of the experiments the object that changed color was the same shape (trained shape) on every trial. Participants were not explicitly aware of this change probability manipulation and change detection performance was not improved for the trained shape versus untrained shapes. In two of the experiments, the object that changed color was always in the same general location (trained location). Although participants were not explicitly aware of the change probability, implicit knowledge of it did improve change detection performance in the trained location. These results indicate that improved change detection performance through implicitly learned change probability occurs for location but not shape.     

The roles of encoding,retrieval, and awareness

In the experiment reported here, we examined the processes by which expected (probable) changes are detected more frequently than are unexpected (improbable) changes (the change probability effect; Beck, Angelone, & Levin, 2004). The change probability effect may be caused by a bias toward probable changes during encoding of the prechange aspect, during retrieval of the prechange aspect, or during activation of an explicit response to the change. Participants performed a change detection task for probable and improbable changes while their eye movements were tracked. Change detection performance was superior for probable changes, but long-term memory performance was equivalent for both probable and improbable changes. Therefore, although both probable and improbable prechange aspects were encoded, probable prechange aspects were more likely to be retrieved during change detection. Implicit change detection was also greater for probable changes than for improbable changes, suggesting that the change probability effect is the result of a bias during the retrieval and comparison stage of change detection. The stimuli used in the change detection task may be downloaded from www.psychonomic.org/archive.     

Knowledge about the probability of change affects change detection performance

The visual system continually selects some information for processing while bypassing the processing of other information, and as a consequence, participants often fail to notice large changes to visual stimuli. In the present studies, the authors investigated whether knowledge about the probability of particular changes occurring over time increased the likelihood that changes that were likely to occur in the real world (probable changes) would be detected. The results of two experiments showed that participants were more likely to detect probable changes. This occurred whether or not they were processing the scene in a meaningful manner or actively searching the scene for changes. Furthermore, participants were unable to accurately predict change detection performance for probable and improbable changes.     

Knowing where is different from knowing what: Distinct response time profiles and accuracy effects for target location,orientation, and color probability

When a location is cued, targets appearing at that location are detected more quickly. When a target feature is cued, targets bearing that feature are detected more quickly. These attentional cueing effects are only superficially similar. More detailed analyses find distinct temporal and accuracy profiles for the two different types of cues. This pattern parallels work with probability manipulations, where both feature and spatial probability are known to affect detection accuracy and reaction times. However, little has been done by way of comparing these effects. Are probability manipulations on space and features distinct? In a series of five experiments, we systematically varied spatial probability and feature probability along two dimensions (orientation or color). In addition, we decomposed response times into initiation and movement components. Targets appearing at the probable location were reported more quickly and more accurately regardless of whether the report was based on orientation or color. On the other hand, when either color probability or orientation probability was manipulated, response time and accuracy improvements were specific for that probable feature dimension. Decomposition of the response time benefits demonstrated that spatial probability only affected initiation times, whereas manipulations of feature probability affected both initiation and movement times. As detection was made more difficult, the two effects further diverged, with spatial probability disproportionally affecting initiation times and feature probability disproportionately affecting accuracy. In conclusion, all manipulations of probability, whether spatial or featural, affect detection. However, only feature probability affects perceptual precision, and precision effects are specific to the probable attribute.     

Feature binding in visual short-term memory is unaffected by task-irrelevant changes of location,shape, and color

Three experiments used a change detection paradigm across a range of study–test intervals to address the respective contributions of location, shape, and color to the formation of bindings of features in sensory memory and visual short-term memory (VSTM). In Experiment 1, location was designated task irrelevant and was randomized between study and test displays. The task was to detect changes in the bindings between shape and color. In Experiments 2 and 3, shape and color, respectively, were task irrelevant and randomized, with bindings tested between location and color (Experiment 2) and location and shape (Experiment 3). At shorter study–test intervals, randomizing location was most disruptive, followed by shape and then color. At longer intervals, randomizing any task-irrelevant feature had no impact on change detection for bindings between features, and location had no special role. Results suggest that location is crucial for initial perceptual binding but loses that special status once representations are formed in VSTM, which operates according to different principles, than do visual attention and perception.     

The role of attention in processing configural and shape information in 3-D novel objects

Recent research suggests that there is an advantage for processing configural information in scenes and objects. The purpose of this study was to investigate the extent to which attention may account for this configural advantage. In Experiment 1, we found that cueing the location of change in single object displays improved detection performance for both configural and shape changes, yet cueing attention away from the location of change was detrimental only for shape change detection. A configural advantage was present for each cueing condition. Experiments 2A and 2B examined whether the configural advantage persisted in conditions where attention was distributed more widely, using a visual search paradigm. Although searches for configural changes were faster than those for shape changes across all set sizes, both types of information appeared to be processed with similar efficiency. Overall, these results suggest that the configural advantage is independent of the location or distribution of visual attention.     

No evidence for binding of items to task-irrelevant backgrounds in visual working memory

When representing visual features such as color and shape in visual working memory (VWM), participants also represent the locations of those features as a spatial configuration of the locations of those features in the display. In everyday life, we encounter objects against some background, yet it is unclear whether the configural representation in memory obligatorily constitutes the entire display, including that (often task-irrelevant) background information. In three experiments, participants completed a change detection task on color and shape; the memoranda were presented in front of uniform gray backgrounds, a textured background (Exp. 1), or a background containing location placeholders (Exps. 2 and 3). When whole-display probes were presented, changes to the objects’ locations or feature bindings impacted memory performance—implying that the spatial configuration of the probes influenced participants’ change decisions. Furthermore, when only a single item was probed, the effect of changing its location or feature bindings was either diminished or completely extinguished, implying that single probes do not necessarily elicit the entire spatial configuration. Critically, when task-irrelevant backgrounds were also presented that may have provided a spatial configuration for the single probes, the effect of location or bindings was not moderated. These findings suggest that although the spatial configuration of a display guides VWM-based recognition, this information does not necessarily always influence the decision process during change detection.     

The influence of location and visual features on visual object memory

In five experiments, we examined the influence of contextual objects’ location and visual features on visual memory. Participants’ visual memory was tested with a change detection task in which they had to judge whether the orientation (Experiments 1A, 1B, and 2) or color (Experiments 3A and 3B) of a target object was the same. Furthermore, contextual objects’ locations and visual features were manipulated in the test image. The results showed that change detection performance was better when contextual objects’ locations remained the same from study to test, demonstrating that the original spatial configuration is important for subsequent visual memory retrieval. The results further showed that changes to contextual objects’ orientation, but not color, reduced orientation change detection performance; and changes to contextual objects’ color, but not orientation, impaired color change detection performance. Therefore, contextual objects’ visual features are capable of affecting visual memory. However, selective attention plays an influential role in modulating such effects.     

Latencies to name one of three stimulus dimensions: A study of probability effects and dimension integrality

Following each of 400 stimuli that varied according to three binary dimensions (location, color, and shape), subjects named the value of one particular dimension as quickly as possible. Each stimulus appeared on the “left” and “right” side of a screen (location dimension), and was a “red” or “green” triangle (color dimension) with apex oriented “up” or “down” (shape dimension). The alternatives of each dimension varied according to different probability distributions (90/10, 70/30, or 50/50), and three schedule conditions were contrived so that each distribution occurred once for each dimension. Nine groups of 10 subjects each defined the factorial of 3 (response conditions: identify location, color, or shape) by 3 (schedule conditions: 90 left/70 red/50 down, 70 left/50 red/90 down, or 50 left/90 red/70 down). Latencies to identify the shape dimension were influenced reliably by the probabilities of both response-relevant and response-irrelevant stimuli. Shape probabilities did not affect latencies to identify location of color, but these latencies were significantly influenced by both color and location probabilities. Results are discussed with reference to the locus of the stimulus probability effect and dimensional integrality.     

Comparing view sensitivity in shape discrimination with shape sensitivity in view discrimination

In three picture-picture matching experiments, the effects of a view change on our ability to detect a shape change (Experiments 1 and 2) were contrasted with the effects of a shape change on our ability to detect a view change (Experiment 3). In each experiment, both view changes and shape changes influenced performance. However, shape changes had more influence than did view changes in the shape change detection task Conversely, view changes were more influential when the task was to detect view changes. Thus, the participants could often discriminate between the effects of shape changes and the effects of view changes. The disruptive effect of task-irrelevant changes (view changes in the first two experiments; shape changes in the final experiment) does not support Stankiewicz's (2002) claim that information about viewpoint and about shape can be estimated independently by human observers. However, the greater effect of variation in the task-relevant than in the task-irrelevant dimension indicates that the observers were moderately successful at disregarding irrelevant changes.     

Display-control arrangement correspondence and logical recoding in the Hedge and Marsh reversal of the Simon effect

When left and right keypresses are made to stimuli in left and right locations, and stimulus location is irrelevant to the task, responses are typically faster when stimulus location corresponds with response location than when it does not (the Simon effect). This effect reverses when the relevant stimulus-response mapping is incompatible, with responses being slower when stimulus and response locations correspond (the Hedge and Marsh reversal). Simon et al. (Acta Psychol. 47 (1981) 63) reported an exception to the Hedge and Marsh reversal for a situation in which the relevant stimulus dimension was the color of a centered visual stimulus and the irrelevant location information was left or right tone location. In contrast, similar experiments have found a reversal of the Simon effect for tone location when relevant visual locations were mapped incompatibly to responses. We conducted four experiments to investigate this discrepancy. Both results were replicated. With an incompatible mapping, irrelevant tone location showed a small reverse Simon effect when the relevant visual dimension was physical location but not when the color of a centered stimulus or the direction in which an arrow pointed conveyed the visual location information. The reversal occurred in a more standard Hedge and Marsh task in which the irrelevant dimension was location of the colored stimulus, but only when the response keys were visibly labeled. Several of the results suggest that display-control arrangement correspondence is the primary cause of the Hedge and Marsh reversal, with logical recoding playing only a secondary role.     

Visual search for singleton feature targets across dimensions: Stimulus- and expectancy-driven effects in dimensional weighting

Four pop-out search experiments investigated whether dimension-based visual attention is top-down modulable. Observers searched for singleton feature targets defined, variably across trials, by a color or an orientation difference to nontargets. Observers were precued to the most probable target-defining dimension (e.g., by the word color) or feature (red) on a given trial. Results revealed expedited reaction times (RTs) for valid-dimension targets relative to neutral-cue conditions, and slowed RTs for invalid-dimension targets. Cue information as to precise target feature yielded some extra effect only for color targets. The dimensional cuing significantly reduced, but did not abolish, the dimension-specific influence of the previous target on detection of the current target (same-dimension RT < different-dimension RT). These findings confirm that top-down dimensional set modulates stimulus-driven dimension processes in the detection of pop-out signals. ((c) 2003 APA, all rights reserved)     

Target location probability effects in visual search: an effect of sequential dependencies

Target location probability was manipulated in a visual search task. When the target was twice as likely to appear on 1 side of the display as the other, manual button-press response times were faster (Experiment 1A) and first saccades were more frequently directed (Experiment 1B) to the more probable locations. When the target appeared with equal probability at each location in this search task, performance benefited from repetition of target location in the preceding trials (Experiment 2). When the trial sequence was constrained so that target location did not repeat within a series of 4 trials, there was no longer an advantage for more probable locations (Experiment 3). The authors conclude that the search benefits for more probable locations resulted from short-term target location repetitions.     

How retaining objects containing multiple features in visual working memory regulates the priority for access to visual awareness

The content of visual working memory influences the access to visual awareness. Thus far, research has focused on retention of a single feature, whereas memoranda in real life typically contain multiple features. Here, we intermixed a delayed match-to-sample task to manipulate VWM content, and a breaking Continuous Flash Suppression (b-CFS) task to measure prioritization for visual awareness. Observers memorized either the color (Exp. 1), the shape (Exp. 2) or both the features (Exp. 3) of an item and indicated the location of a suppressed target. We observed that color-matching targets broke suppression faster than color-mismatching targets both when color was memory relevant or irrelevant. Shape only impacted priority for visual awareness through an interaction with color. We conclude that: (1) VWM can regulate the priority of visual information to access visual awareness along a single feature dimension; (2) different features of a memorandum vary in their potency to impact access to visual awareness, and the more dominant feature may even suppress the effect of the less dominant feature; (3) even stimuli that match an irrelevant feature dimension of the memorandum can be prioritized for visual awareness.     

Visual marking and visual change

Five experiments investigated the types of changes that disrupt the preview effect--the benefit gained in difficult search tasks from presenting some distractors earlier in time. A shape change with or without an overall luminance change at the location of an old item was found to disrupt the preview effect, whereas an equivalent luminance change alone or an isoluminant color change was not disruptive. Results suggest that (a) relatively low-level visual changes may not be sufficient to abolish the benefit, (b) the benefit most likely occurs through inhibition applied to locations within a location master map, and (c) inhibition need not be applied to surface features of objects.     

Accessing long-term memory representations during visual change detection

In visual change detection tasks, providing a cue to the change location concurrent with the test image (post-cue) can improve performance, suggesting that, without a cue, not all encoded representations are automatically accessed. Our studies examined the possibility that post-cues can encourage the retrieval of representations stored in long-term memory (LTM). Participants detected changes in images composed of familiar objects. Performance was better when the cue directed attention to the post-change object. Supporting the role of LTM in the cue effect, the effect was similar regardless of whether the cue was presented during the inter-stimulus interval, concurrent with the onset of the test image, or after the onset of the test image. Furthermore, the post-cue effect and LTM performance were similarly influenced by encoding time. These findings demonstrate that monitoring the visual world for changes does not automatically engage LTM retrieval.     

Attending to faces: change detection,familiarization, and inversion effects

We tested detection of changes to eye position, eye color (brightness), mouth position, and mouth color in frontal views of faces. Two faces were presented sequentially for 555 ms each, with a blank screen of 120 ms separating the two. Faces were presented either both upright or both inverted. Measures of detection (d') were calculated for several different degrees of change for each of the four dimensions of change. We first compared results to an earlier experiment that used an oddity design, in which subjects indicated which of three simultaneously viewed and otherwise identical faces had been altered on one of these four dimensions. Subjects in both of these experiments were partially cued, in that they knew the four possible types of changes that could occur on a given trial. The change-detection results correlated well with the oddity data. They confirmed that face inversion had little effect upon detection of changes in eye color, a moderate effect upon detection of eye-position or mouth-color changes, and caused a drastic reduction in the detection of mouth-position changes. An experiment in which uncued and fully cued subjects were compared showed that cueing significantly improved detection of feature color changes, but there was little difference between upright and inverted faces. Full cueing eliminated all effects of inversion. Compared to partial cueing, changes in mouth color were poorly detected by uncued subjects. Last, a change in the frequency of the base (unaltered) face in an experiment from 75% to 40% showed that increased short-term familiarity decreased the detection of eye changes and increased the detection of mouth changes, regardless of face orientation and the type of change made (color or position). We conclude that uncued subjects encode the spatial relations of features more than the colors of features, that mouth color in particular is not considered a relevant dimension for encoding, and that familiarization redistributes attention from more to less salient facial regions. Inversion effects are not simply an exaggeration of the salience effects revealed by withdrawing cueing, but represent an interaction of spatial encoding with salience, in that the greatest inversion effects occur for spatial shifts in less salient facial regions, and can be eliminated through the use of focused attention.     

视觉客体工作记忆中图形特征存储与捆绑时程

采用单探测变化检测范式,考察了形状和颜色客体在工作记忆中的表征方式、特征检测类型及初始刺激呈现时间对工作记忆表征的影响。结果表明:(1)视觉客体工作记忆的表征包括两个水平,首先是对客体的特征进行加工存储,其次才是对特征的捆绑;(2)不同特征的加工时间不同,颜色的加工完成的较早,记忆效果好,而形状的加工完成的较晚,记忆效果也差,表现出颜色的子系统优势;(3)特征的捆绑不是必需的,只有在任务需要时才进行,并且捆绑的过程符合特征捆绑的双阶段理论。     

The enhanced Simon effect for older adults is reduced when the irrelevant location information is conveyed by an accessory stimulus

The Simon effect, better performance when irrelevant stimulus location corresponds with the response location than when it does not, typically is larger for older than younger adults. However, Simon and Pouraghabagher [Simon, R. J., & Pouraghabagher, A. R. (1978). The effect of aging on the stages of processing in a choice reaction time task. Journal of Gerontology, 33, 553-561] found no age difference using an accessory-stimulus Simon task in which the relevant dimension was the color of a visual stimulus and the irrelevant dimension the location of a tone. Experiment 1 confirmed that older adults show a larger Simon effect than younger adults for the visual Simon task and that this age-related deficit is reduced or eliminated for the auditory-accessory task. Experiment 2 provided evidence suggesting that a small part of the age-related deficit in the visual Simon task is due to having to code the location of the relevant stimulus, but Experiment 3 showed that the majority of the deficit is due to the relevant and irrelevant information being conveyed by the same stimulus. Reaction-time distribution analyses show similar functions for younger and older adults, suggesting that the time course of activation is similar for both age groups.     

Life-span development of visual working memory: when is feature binding difficult?

We asked whether the ability to keep in working memory the binding between a visual object and its spatial location changes with development across the life span more than memory for item information. Paired arrays of colored squares were identical or differed in the color of one square, and in the latter case, the changed color was unique on that trial (item change) or was duplicated elsewhere in the array (color-location binding change). Children (8-10 and 11-12 years old) and older adults (65-85 years old) showed deficits relative to young adults. These were only partly simulated by dividing attention in young adults. The older adults had an additional deficiency, specifically in binding information, which was evident only when item- and binding-change trials were mixed together. In that situation, the older adults often overlooked the more subtle, binding-type changes. Some working memory processes related to binding undergo life-span development in an inverted-U shape, whereas other, bias- and salience-related processes that influence the use of binding information seem to develop monotonically.