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.     

Connectedness affects dot numerosity judgment: Implications for configural processing

Participants judged the number of dots in visual displays with brief presentations (200 msec), such that the numerosity judgment was based on an instantaneous impression without counting. In some displays, pairs of adjacent dots were connected by line segments, whereas, in others, line segments were freely hanging without touching the dots. In Experiments 1, 2A, and 2B, connecting pairs of dots by line segments led to underestimation of dot numbers in those patterns. In Experiment 3, we controlled for the number of freely hanging line segments, whereas Experiment 4 showed that line segments that were merely attached to dots without actually connecting them did not produce a considerable underestimation effect. Experiment 5 showed that a connectedness effect existed when stimulus duration was reduced (50 msec) or extended (1,000 msec). We conclude that connectivity affects dot numerosity judgments, consistent with earlier findings of a configural effect in numerosity processing. Implications of the role of connectedness in object representation are discussed.     

Object-based attention: strength of object representation and attentional guidance

Two or more features belonging to a single object are identified more quickly and more accurately than are features belonging to different objects--a finding attributed to sensory enhancement of all features belonging to an attended or selected object. However, several recent studies have suggested that this "single-object advantage" may be a product of probabilistic and configural strategic prioritizations rather than of object-based perceptual enhancement per se, challenging the underlying mechanism that is thought to give rise to object-based attention. In the present article, we further explore constraints on the mechanisms of object-based selection by examining the contribution of the strength of object representations to the single-object advantage. We manipulated factors such as exposure duration (i.e., preview time) and salience of configuration (i.e., objects). Varying preview time changes the magnitude of the object-based effect, so that if there is ample time to establish an object representation (i.e., preview time of 1,000 msec), then both probability and configuration (i.e., objects) guide attentional selection. If, however, insufficient time is provided to establish a robust object-based representation, then only probabilities guide attentional selection. Interestingly, at a short preview time of 200 msec, when the two objects were sufficiently different from each other (i.e., different colors), both configuration and probability guided attention selection. These results suggest that object-based effects can be explained both in terms of strength of object representations (established at longer exposure durations and by pictorial cues) and probabilistic contingencies in the visual environment.     

The role of the head in configural body processing: Behavioural and electrophysiological evidence from the inversion and scrambling effect

The present study aimed to further explore the role of the head for configural body processing by comparing complete bodies with headless bodies and faceless heads (Experiment 1). A second aim was to further explore the role of the eye region in configural face processing (Experiment 2). Due to that, we conducted a second experiment with complete faces, eyeless faces, and eyes. In addition, we used two effects to manipulate configural processing: the effect of stimulus inversion and scrambling. The current data clearly show an inversion effect for intact bodies presented with head and faces including the eye region. Thus, the head and the eye region seem to be central for configural processes that are manipulated by the effect of stimulus inversion. Furthermore, the behavioural and electrophysiological body inversion effect depends on the intact configuration of bodies and is associated with the N170 as the face inversion effect depends on the intact face configuration. Hence, configural body processing depends not only on the presence of the head but rather on a complete representation of human bodies that includes the body and the head. Furthermore, configural face processing relies on intact and complete face representations that include faces and eyes.     

Hemispheric asymmetries for temporal information processing: transient detection versus sustained monitoring

This study investigated functional differences in the processing of visual temporal information between the left and right hemispheres (LH and RH). Participants indicated whether or not a checkerboard pattern contained a temporal gap lasting between 10 and 40 ms. When the stimulus contained a temporal signal (i.e. a gap), responses were more accurate for the right visual field-left hemisphere (RVF-LH) than for the left visual field-right hemisphere (LVF-RH). This RVF-LH advantage was larger for the shorter gap durations (Experiments 1 and 2), suggesting that the LH has finer temporal resolution than the RH, and is efficient for transient detection. In contrast, for noise trials (i.e. trial without temporal signals), there was a LVF-RH advantage. This LVF-RH advantage was observed when the entire stimulus duration was long (240 ms, Experiment 1), but was eliminated when the duration was short (120 ms, Experiment 2). In Experiment 3, where the gap was placed toward the end of the stimulus presentation, a LVF-RH advantage was found for noise trials whereas the RVF-LH advantage was eliminated for signal trials. It is likely that participants needed to monitor the stimulus for a longer period of time when the gap was absent (i.e. noise trials) or was placed toward the end of the presentation. The RH may therefore be more efficient in the sustained monitoring of visual temporal information whereas the LH is more efficient for transient detection.     

Multidimensional shape similarity in the development of visual object classification

The current work examined age differences in the classification of novel object images that vary in continuous dimensions of structural shape. The structural dimensions employed are two that share a privileged status in the visual analysis and representation of objects: the shape of discrete prominent parts and the attachment positions of those parts. Experiment 1 involved a triad classification task in which participants at each of three different ages (5 years, 8 years, and adult) classified object images from two distinct stimulus sets. Across both sets, the youngest children demonstrated a systematic bias toward the shape of discrete parts during their judgments. With increasing age, participants increasingly came to select both the shape and the position of parts when classifying the images. The findings from Experiment 2 indicate that the local shape bias observed in young children's classifications is not merely a consequence of a discrimination advantage for that dimension. Results are discussed in relation to corresponding age-related changes in other functional contexts of visual processing.     

Reflex inhibition in humans: Sensitivity to brief silent periods in white noise

A white noise (60 dB SPL) was always present except for brief silent periods (“gaps”) which occurred just before an eyelid reflex was elicited in human volunteers by a brief innocuous shock to the forehead. In Experiment 1 (n=8), 10-msec gaps (“S1”) were given 40, 80, 120, 160, or 200 msec before the shock (“S2”). Compared with S2-alone trials, the reflex was inhibited by about 50% at intervals of 80 msec and beyond. Experiment 2 (n=12) first provided detection thresholds for gaps using a simple version of the method of limits: on average a gap of 5.4 msec duration was just detected. Then gaps of 0, 2, 4, 6, 8, and 10 msec were given in random order, each 100 msec before S2. The 4-msec stimulus was an effective inhibitor of the reflex, and inhibition further increased on to 6- and then to 8-msec durations. A comparison of the values obtained on reflex inhibition with the 5.4-msec threshold obtained with the conventional psycho-physical test reveals that in humans reflex inhibition provides an objective index of stimulus detection that is at least of sufficient sensitivity to warrant its clinical application. The steady increase in reflex inhibition as gap duration increased from 2 to 8 msec may be of significance for tracing the rate of decay of afferent stimulation following noise offset, as it presumably reflects the growing sensitivity to the resumption of the noise as the duration of the silent period is increased.     

A configural effect in visual short-term memory for features from different parts of an object

Previous studies have shown that change detection performance is improved when the visual display holds features (e.g., a colour and an orientation) that are grouped into different parts of the same object compared to when they are all spatially separated (Xu, 2002a, 2002b). These findings indicate that visual short-term memory (VSTM) encoding can be "object based". Recently, however, it has been demonstrated that changing the orientation of an item could affect the spatial configuration of the display (Jiang, Chun, & Olson, 2004), which may have an important influence on change detection. The perceptual grouping of features into an object obviously reduces the amount of distinct spatial relations in a display and hence the complexity of the spatial configuration. In the present study, we ask whether the object-based encoding benefit observed in previous studies may reflect the use of configural coding rather than the outcome of a true object-based effect. The results show that when configural cues are removed, the object-based encoding benefit remains for features (i.e., colour and orientation) from different parts of an object, but is significantly reduced. These findings support the view that memory for features from different parts of an object can benefit from object-based encoding, but the use of configural coding significantly helps enlarge this effect.     

Testing a conceptual locus

Changes to objects that are inconsistent with the scene in which they appear are detected more accurately than changes to consistent objects. In three experiments, we tested whether this inconsistent object advantage derives from the differential retention of conceptual codes generated from a brief view of a real-world scene in accordance with a conceptual short-term memory (CSTM) hypothesis. A scene was presented for 250 msec, followed by a brief mask and a test scene in which a target object was either changed or not changed. In Experiment 1, changes that altered conceptual content (object deletion) were contrasted with visual changes (left-right orientation changes). In Experiment 2, the duration of the mask was manipulated to vary the amount of time available for conceptual consolidation of the initial scene. In Experiment 3, the type of mask was manipulated: Either a meaningless pattern mask or a meaningful, and thus conceptually disruptive, scene was shown. The inconsistent object advantage was obtained in each experiment, yet in none was it modulated in the direction predicted by the CSTM hypothesis. Instead, the inconsistent object advantage is likely to be caused by contextual influence on memory for visual object representations.     

Postsaccadic processing of the retinal image during picture scanning

Eye movements were monitored while observers inspected photographs of natural scenes. At the end of each saccade (i.e., at the beginning of each period of steady fixation), the stimulus was replaced for a certain period of time by a uniform field (Experiment 1) or a blurred version of the stimulus scene (Experiment 2). Total fixation duration was measured as a function of the duration of the initial uniform field or the blurred image that followed the saccade. It was found that fixation duration increased proportionally with the duration of the initial replacement field, even for durations as short as 25 msec. These results suggest that the visual system uses information on the retina right after each saccade is completed and that the blurred, low-resolution information used in Experiment 2 (cutoff frequency of 0.8 cpd) is not sufficient for the requirements of picture processing in this task.     

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.     

Duration discrimination of empty and filled intervals marked by auditory and visual signals

Experiments 1 and 2 compared, with a single-stimulus procedure, the discrimination of filled and empty intervals in both auditory and visual modalities. In Experiment 1, in which intervals were about 250 msec, the discrimination was superior with empty intervals in both modalities. In Experiment 2, with intervals lasting about 50 msec, empty intervals showed superior performance with visual signals only. In Experiment 3, for the auditory modality at 250 msec, the discrimination was easier with empty intervals than with filled intervals with both the forced-choice (FC) and the single stimulus (SS) modes of presentation, and the discrimination was easier with the FC than with the SS method. Experiment 4, however, showed that at 50 and 250 msec, with a FC-adaptive procedure, there were no differences between filled and empty intervals in the auditory mode; the differences observed with the visual mode in Experiments 1 and 2 remained significant. Finally, Experiment 5 compared differential thresholds for four marker-type conditions, filled and empty intervals in the auditory and visual modes, for durations ranging from .125 to 4 sec. The results showed (1) that the differential threshold differences among marker types are important for short durations but decrease with longer durations, and (2) that a generalized Weber’s law generally holds for these conditions. The results as a whole are discussed in terms of timing mechanisms.     

Effects of contrast polarity in paracontrast masking

The visibility of a target stimulus can be suppressed (inhibition) or increased (facilitation) during paracontrast masking. Three processes have been proposed to be involved in paracontrast masking: brief inhibition, facilitation, and prolonged inhibition (Breitmeyer et al., 2006). Brief inhibition is observed when the mask precedes the target at short stimulus onset asynchronies (SOAs) ranging from -10 to -30 msec, whereas prolonged inhibition is effective up to very large SOAs of -450 msec. Facilitation, enhancement in target visibility, can be observed at SOA values between -20 and -110 msec. We further investigated these processes by changing target-mask spatial separation and the contrast polarity of the mask. Our results show that (1) facilitation weakens when spatial separation between the target and mask is increased or when they have opposite contrast polarity, and (2) brief inhibition turns into facilitation for the opposite-polarity mask, whereas prolonged inhibition does not change significantly. These results suggest a fast inhibition mechanism realized in the contrast-specific center-surround antagonism of classical receptive fields for brief inhibition and a slower, higher level cortical processing that is indifferent to contrast polarity for prolonged inhibition.     

Emotion recognition: The role of featural and configural face information

Several studies investigated the role of featural and configural information when processing facial identity. A lot less is known about their contribution to emotion recognition. In this study, we addressed this issue by inducing either a featural or a configural processing strategy (Experiment 1) and by investigating the attentional strategies in response to emotional expressions (Experiment 2). In Experiment 1, participants identified emotional expressions in faces that were presented in three different versions (intact, blurred, and scrambled) and in two orientations (upright and inverted). Blurred faces contain mainly configural information, and scrambled faces contain mainly featural information. Inversion is known to selectively hinder configural processing. Analyses of the discriminability measure (A′) and response times (RTs) revealed that configural processing plays a more prominent role in expression recognition than featural processing, but their relative contribution varies depending on the emotion. In Experiment 2, we qualified these differences between emotions by investigating the relative importance of specific features by means of eye movements. Participants had to match intact expressions with the emotional cues that preceded the stimulus. The analysis of eye movements confirmed that the recognition of different emotions rely on different types of information. While the mouth is important for the detection of happiness and fear, the eyes are more relevant for anger, fear, and sadness.     

Configural encoding in visual feature binding

The role of configural encoding in feature binding was assessed using the change detection paradigm. Experiment 1 studied the relevance of location in colour–shape binding with study–test intervals ranging from 0 to 4100 ms. Location was rendered irrelevant by randomising it from study to test display or was kept unchanged from study to test. Results revealed differences between these two conditions at 0 and 200 ms, but not at 1500, 2800, and 4100 ms, suggesting that location was important for feature binding in the initial stages, but performance at longer study–test intervals was impervious to change in locations. Experiment 2 studied the effect of increasing the study-display duration by comparing performance with display durations of 200, 900, and 1500 ms, at the study test intervals of 0 and 2000 ms. Although, there was a general increase in the level of performance with increasing display duration, the interaction effect obtained in Experiment 1 was replicated. Experiments 3 and 4 studied the effect of sequential presentation of stimuli, otherwise retaining the design and procedure of Experiment 2. Different levels of performance in Experiments 2, 3, and 4 revealed the role of configural encoding in the binding process.     

Facial expression recognition in peripheral versus central vision: role of the eyes and the mouth

This study investigated facial expression recognition in peripheral relative to central vision, and the factors accounting for the recognition advantage of some expressions in the visual periphery. Whole faces or only the eyes or the mouth regions were presented for 150 ms, either at fixation or extrafoveally (2.5° or 6°), followed by a backward mask and a probe word. Results indicated that (a) all the basic expressions were recognized above chance level, although performance in peripheral vision was less impaired for happy than for non-happy expressions, (b) the happy face advantage remained when only the mouth region was presented, and (c) the smiling mouth was the most visually salient and most distinctive facial feature of all expressions. This suggests that the saliency and the diagnostic value of the smile account for the advantage in happy face recognition in peripheral vision. Because of saliency, the smiling mouth accrues sensory gain and becomes resistant to visual degradation due to stimulus eccentricity, thus remaining accessible extrafoveally. Because of diagnostic value, the smile provides a distinctive single cue of facial happiness, thus bypassing integration of face parts and reducing susceptibility to breakdown of configural processing in peripheral vision.     

Similarity modulates the face-capturing effect in change detection

We investigated whether similarity among faces could modulate the face-capturing effect in change detection. In Experiment 1, a singleton search task was used to demonstrate that a face stimulus captures attention and the odd-one-out hypothesis cannot account for the results. Searching for a face target was faster than searching for a nonface target no matter whether distractor–distractor similarity was low or high. The fast search, however, did not lead to a face-detection advantage in Experiment 2 when the pre- and postchange faces were highly similar. When participants in Experiment 3 had to divide their attention between two faces in stimulus displays for change detection, detection performance was worse than performance in detecting nonface changes. The face-capturing effect alone is insufficient to produce the face-detection advantage. Face processing is efficient but its effect on performance depends on the stimulus–task context.     

Spatial-frequency-dependent visible persistence and specific reading disability

Visible persistence duration for sine-wave gratings was measured in 9-year-old normal and specific-reading-disabled children. Experiment 1 investigated the influence of stimulus duration on visible persistence. The results demonstrated a Reading Group X Spatial Frequency interaction with disabled readers showing a smaller increase in persistence duration with increasing spatial frequency than controls. This interaction was greatest with stimulus durations longer than 80 msec. In Experiments 2a and 2b persistence was measured across a range of contrasts from .1 to .5. The stimulus durations employed were 100 msec in Experiment 2a and 300 msec in Experiment 2b. In both experiments, increasing contrast decreased persistence duration at 2 and 12 cycles per degree (c/deg) for the control group. In the specific-reading-disabled group, however, contrast had little effect on the persistence of 2-c/deg gratings in either experiment. In Experiment 2a the persistence of the 12-c/deg grating decreased with increasing contrast for both groups. In Experiment 2b contrast had significantly less effect on persistence duration in the specific-reading-disabled group, however, contrast had little effect on the persistence of 2-c/deg ratings in either experiment. In Experiment 2b contrast had significantly less effect on persistence duration in the specific-reading-disabled group than in the control group at 12 c/deg. Consequently, contrast had less effect on persistence in specific-reading-disabled children than in normal readers, especially at durations longer than the "critical duration" for each spatial frequency. Experiment 3 extended this finding to gratings with spatial frequencies of 4 and 8 c/deg. These results indicate a difference between normal and specific-reading-disabled children in cortical visible persistence. Two scores of visual processing were derived from the above experiments. On these scores the reading-disabled children were divided into Visual Disabled Readers (approximately 70%--eight subjects) and Nonvisual Disabled Readers (approximately 30%--four subjects). The percentages of disabled readers in each category remained constant when the sample size was increased to 61 normal and disabled readers.