Principles of feature integration in visual perception.
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Adult↗
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Results for “Pattern Recognition, Visual”
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Trees as memory representations for simple visual patterns.
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Adolescent↗
Visual hallucinations of the pattern type.
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Form Perception↗
Temporal determinants of spatial sine-wave masking.
A temporal forced-choice procedure was used to measure the contrast threshold for a sinusoidal test grating (spatial frequency - f) superimposed upon a sinusoidal background or masking grating (spatial frequency = 3f). The spatial contrast of the background grating was varied, and threshold measurements were made at each of a number of background contrasts to describe a threshold versus masking contrast (tvc) function. Tvc functions were obtained when the background and test grating contrasts were, independently of each other, held steady (0 Hz) or modulated at 5 Hz. The changes of temporal modulation frequency affected the slopes of the tvc functions. In some cases the tve functions for steady and flickering test gratings crossed one another. The changes of slope suggest, and the crossovers imply, that some steady and flickering patterns are detected by separate visual mechanisms.
Form Perception↗
Meridional anisotropy in visual processing: implications for the neural site of the oblique effect.
The contention is examined that the oblique effect, i.e., the well-known performance deficit in detecting orientation difference in oblique lines as compared to vertical and horizontal ones, has its origin in a relative deficiency of neurons with obliquely-oriented receptive fields in the primary visual cortex. Psychophysical observations demonstrate a prominent oblique effect also in visual tasks involving widely-separated elements and other stimuli that would elicit little or no response in oriented neurons in the visual cortex. Conversely, some tasks, e.g. position discrimination, exhibit no oblique effect even with short, high-contrast lines. When the comparison with the reference can be accomplished during a single brief exposure rather than sequential ones, thresholds for orientation differences between adjacent contours in oblique meridians are also elevated compared to those in the vertical and horizontal, but to a lesser extent. In one particular texture discrimination task some but not all observers have a conspicuous oblique effect. The discrimination only of the direction of streaming random dots, not of their speed, is poorer for motions in oblique meridians. The findings imply that the neural locus for the oblique effect is more central than the primary visual cortex.
Contrast Sensitivity↗
Some plane truths about pictures: notes on Wagemans, Lamote, and van Gool (1997).
Wagemans, Lamote, and van Gool (1997) have attempted to show that observers can determine the geometric equivalence of shapes seen in perspective, or in projective transformation. Artifacts of measurement in their procedures forestall such a conclusion. Their experiment fails to control projective properties adequately, and also confounds the transformations of shear and compression. Their evidence that observers can discern the equivalence of shapes under perspective can be reconstrued as evidence for sensitivity to different, unrelated properties: to the plane compression that follows from the depiction of flat shapes in perspective, and to gross differences in shape not specific to projective geometry. An improved set of procedures is proposed for the measurement of stimuli in the study of visual shape constancy.
Artifacts↗
Modulation of backward pattern masking by focal visual attention.
The effect of focal visual attention on backward pattern masking was investigated using an orientation discrimination task. The results show that attention reduces primarily the effect of interruption masking, the later component of pattern masking, which occurs when the delay between the target and mask onset is about 50-150 ms. The strongest spatial cueing effect, i.e. the strongest reduction of the orientation discrimination threshold due to focal attention, was observed at intermediate (approximately 100 ms) target-to-mask stimulus onset asynchrony (SOA). There was a weak effect of cueing at shorter SOAs, and no or a very weak attentional effect was present at longer target-to-mask SOAs, where the pattern masking effect is absent. The dynamics of attentional modulation of backward pattern masking correlates closely with the dynamics of the attentional modulation of neuronal responses in the early visual cortex.
Attention↗
[Effects of symmetry groups on complexity and goodness in visual pattern].
Two experiments were performed to investigate stimulus determinants of pattern complexity and pattern goodness. Two hundred and ninety-six undergraduates rated complexity and goodness of two-dimensional patterns, which consisted of solid and/or open circles. The patterns were invariant under transformations of reflection or rotation, and they formed cyclic groups or dihedral ones. The results were summarized as follows. (1) Goodness of patterns increased with the order of cyclic and dihedral groups with different weights. (2) Complexity of patterns having line-segments decreased with the order of cyclic and dihedral groups with equal weights, whereas that of patterns having no line-segments was medium regardless of the order. (3) Simplicity and goodness of patterns with a vertical axis of reflection were higher than those with the other orientation axes. (4) Patterns consisting of solid circles were rated more complex than those of open ones. (5) Complexity increased as a positively accelerated function of the number of circles, whereas goodness increased as a negatively accelerated function. It was concluded that complexity and goodness were determined by compound factors, which are processed at different stages of human visual system.
Adult↗
Neural and behavioral correlates of emotion recognition in children and adults.
Event-related potentials (ERPs), accuracy scores, and reaction times were used to examine the recognition of emotional expressions. Adults and 7-year-old children saw upright and inverted chromatic slides of the facial expressions of happiness, fear, surprise, and anger, and were asked to press a button for either "happy" or "angry" faces. A positive-going waveform (P300) was apparent at parietal scalp (Pz) and at left and right temporal scalp. Although the behavioral data were similar for both children and adults (e.g., both had more difficulty recognizing angry expressions than happy ones, and angry expressions were more difficult to recognize upside-down than were happy faces), the ERPs indicated that children responded differently than adults did to happy and angry expressions. Adults showed greater P300 amplitude to happy faces, while children showed greater P300 amplitude to angry faces. In addition, for adults, but not children, there were greater P300 amplitude responses at right vs. left temporal scalp.
Adult↗
Lateral asymmetry in testing long-term memory for faces.
Accuracy of recognition memory for faces initially seen in the central visual field was found to be greater 48 hours when previously seen and new faces were presented to the left visual field than when presentation was to for right visual field. It is argued that this result reflects relative specialization for the right hemisphere in storing visual patterns.
Dominance, Cerebral↗
Face recognition memory and configural processing: a developmental ERP study using upright, inverted, and contrast-reversed faces.
The effects of configural changes on faces were investigated in children to determine their role in encoding and recognition processes. Upright, inverted, and contrast-reversed unfamiliar faces were presented in blocks in which one-third of the pictures repeated immediately or after one intervening face. Subjects (8-16 years) responded to repeated faces; event-related potentials were recorded throughout the procedure. Recognition improved steadily with age and all components studied showed age effects reflecting differing maturation processes occurring until adulthood. All children were affected by inversion and contrast-reversal, and face-type effects were seen on latencies and amplitudes of early components (P1 and N170), as well as on later frontal amplitudes. The "old-new" repetition effects (larger amplitude for repeated stimuli) were found at frontal sites and were similar across age groups and face types, suggesting a general working memory system comparably involved in all age groups. These data demonstrate that (1) there is quantitative development in face processing, (2) both face encoding and recognition improve with age, but (3) only encoding is affected by configural changes. The data also suggest a gradual tuning of face processing towards the upright orientation.
Adolescent↗
Recognition memory for unfamiliar faces in Parkinson's disease: behavioral and electrophysiologic measures.
We analyzed event-related potentials (ERPs) and behavioral measurements during a recognition memory task in 15 normal elderly subjects and 15 patients with Parkinson's disease (PD). To elicit ERPs unfamiliar faces were repeated immediately after initial presentation (at lag 0), after one intervening face (at lag 1) or at lag 3. Compared to normal controls, PD patients showed decreased accuracy in recognizing new unfamiliar faces. P170 latency and amplitude were similar between both groups. ERP amplitude between 300 and 500 ms after the stimulus in control subjects showed a positive shift (ERP repetition effect) for lag 0 at all sites and for lag 1 and 3 repetitions at the Fz site, while effects in the PD group were not noted at any site, even for the lag 0 repetition. ERP waveforms for the first presentation of faces in PD patients showed a significant positive shift compared to normal controls. These data suggest intact perception but impaired recognition memory for unfamiliar faces in PD. In addition, recognition memory deficits in PD may result from impairment of comparison of structural representations of presented faces with stored representations of faces known to the observer.
Aged↗
Processing the trees and the forest during initial stages of face perception: electrophysiological evidence.
Although configural processing is considered a hallmark of normal face perception in humans, there is ample evidence that processing face components also contributes to face recognition and identification. Indeed, most contemporary models posit a dual-code view in which face identification relies on the analysis of individual face components as well as the spatial relations between them. We explored the interplay between processing face configurations and inner face components by recording the N170, an event-related potential component that manifests early detection of faces. In contrast to a robust N170 effect elicited by line-drawn schematic faces compared to line-drawn schematic objects, no N170 effect was found if a pair of small objects substituted for the eyes in schematic faces. However, if a pair of two miniaturized faces substituted for the eyes, the N170 effect was restored. Additional experiments ruled out an explanation on the basis of miniaturized faces attracting attention independent of their location in a face-like configuration and show that global and local face characteristics compete for processing resources when in conflict. The results are discussed as they relate to normal and abnormal face processing.
Adolescent↗
Sub-exemplar shape tuning in human face-related areas.
Although human face recognition performance shows high selectivity, even for unfamiliar faces, the neuronal circuitry underlying this high performance is poorly understood. Two extreme alternatives can be considered: either a "labeled-line" principle, in which subtle changes in face images lead to activation of differently tuned neuronal populations, or a coarse coding principle, where the high face selectivity is coded by the relative activation of broadly tuned neurons. In this study, we set to parametrically examine the shape and selectivity profile of face-related visual areas. To that end, we applied the functional magnetic resonance (fMR)-adaptation paradigm. Unfamiliar face stimuli were morphed into sets ranging from identical faces, through subtle morphing, to completely different exemplars. The fusiform face area (FFA) revealed high face sensitivity, so that even facial images perceived as belonging to the same individual (<35%) were sufficient to produce full recovery from adaptation. Interestingly, the psychophysical detectability of facial differences paralleled the release from fMR-adaptation. These results support the labeled-line model where high sensitivity to face changes is paralleled by narrow tuning of neuronal populations selective to each face image, and they suggest that fMR-adaptation is closely related to behavior. The results bear strong implications to the nature of face-related neuronal responses.
Adaptation, Physiological↗
Speed of face recognition in humans: an event-related potentials study.
Event-related potentials (ERPs) were measured while subjects passively looked at a line drawing of a normal face or a line drawing in which parts of the face were scattered so as not to be recognized as a face (scattered face) in order to estimate the speed of face recognition in humans. Because the spatial frequencies of these two types of line drawings were very similar, one could minimize the potentials due to the structure coding stage of the face processing. In addition, passive viewing of these stimuli eliminates the contribution of other processing such as discrimination or memory retrieval. Comparing these two conditions, statistically significant positive potentials were observed in frontal areas from 135ms after stimulus onset for the normal face. These early positive differences were probably due to the face processing per se in human visual recognition. Although statistically significant differences were observed in frontal areas, these are probably related to fusiform or inferior temporal area activation that is often reported using neuro-imaging technologies such as PET or fMRI.
Adult↗
Exploring the functional architecture of person recognition system with event-related potentials in a within- and cross-domain self-priming of faces.
In this paper, we explored the functional properties of person recognition system by investigating the onset, magnitude, and scalp distribution of within- and cross-domain self-priming effects on event-related potentials (ERPs). Recognition of degraded pictures of famous people was enhanced by a prior exposure to the same person's face (within-domain self-priming) or name (cross-domain self-priming) as compared to those preceded by neutral or unrelated primes. The ERP results showed first that the amplitude of the N170 component to famous face targets was modulated by within- and cross-domain self-priming, suggesting not only that the N170 component can be affected by top-down influences but also that this top-down effect crosses domains. Second, similar to our behavioral data, later ERPs to famous faces showed larger ERP self-priming effects in the within-domain than in the cross-domain condition. In addition, the present data dissociated between two topographically and temporally overlapping priming-sensitive ERP components: the first one, with a strongly posterior distribution arising at an early onset, was modulated more by within-domain priming irrespective whether the repeated face was familiar or not. The second component, with a relatively uniform scalp distribution, was modulated by within- and cross-domain priming of familiar faces. Moreover, there was no evidence for ERP-induced modulations for unfamiliar face targets in the cross-domain condition. Together, our findings suggest that multiple neurocognitive events that are possibly mediated by distinct brain loci contribute to face priming effects.
Adult↗
Object recognition: holistic representations in the monkey brain.
Cognitive-psychological and neuropsychological studies suggest that the human brain processes facial information in a distinct manner, relying on mechanisms that are anatomically and functionally different from those underlying the recognition of other objects. Face recognition, for instance, can be disrupted selectively as a result of localized brain damage, and relies strongly on holistic information rather than on the mere processing of local features. Similarly, in the non-human primate, distinct neocortical and limbic structures have cell populations responding specifically to face stimuli and only weakly to other visual patterns. Moreover, such cells tend to respond to the entire configuration of a face rather than to individual facial features. But are faces the only objects represented in this way? Here I present some evidence suggesting that at least one aspect of facial processing, the processing of holistic information, may be employed by the primate brain when recognizing any arbitrary homogeneous class of even artificial objects, which the monkey has to individually learn, remember, and recognize again and again from among a large number of distractors sharing a number of common features with the target. Acquiring such an expertise can induce configurational selectivity in the response of neurons in the visual system. Our findings suggests that regarding their neural encoding faces are unlikely to be 'special', but they rather are the default 'special class' of the primate visual system.
Animals↗
Interaction of top-down and bottom-up processing in the fast visual analysis of natural scenes.
The influence of task requirements on the fast visual processing of natural scenes was studied in 14 human subjects performing in alternation an "animal" categorization task and a single-photograph recognition task. Target photographs were randomly mixed with non-target images and flashed for only 20 ms. Subjects had to respond to targets within 1 s. Processing time for image-recognition was 30-40 ms shorter than for the categorization task, both for the fastest behavioral responses and for the latency at which event related potentials evoked by target and non-target stimuli started to diverge. The faster processing in image-recognition is shown to be due to the use of low-level cues, but source analysis produced evidence that, regardless of the task, the dipoles accounting for the differential activity had the same localization and orientation in the occipito-temporal cortex. We suggest that both tasks involve the same visual pathway and the same decisional brain area but because of the total predictability of the target in the image recognition task, the first wave of bottom-up feed-forward information is speeded up by top-down influences that might originate in the prefrontal cortex and preset lower levels of the visual pathway to the known target features.
Adult↗