Accommodation and stereoacuity

Stereoacuity and resolution acuity were measured (1)through apertures set at various distances from O and (2) through plus lenses producing an accommodative error for the target equal to that produced by the presence of the apertures. Stereoacuity was degraded by the apertures but not by the lenses, whereas resolution acuity was degraded by the lenses but not by the apertures. Although stereoacuity progressively declined with decreasing target distance, it did not change significantly if accommodation remained constant. The decline of stereoacmty in the water ts attributed to increased accommodation resulting from different sources and to a “Ganzfeld” effect of the typical underwater scene.     

How contrast affects stereoacuity

Stereoacuity and its dependence on contrast were measured at four spatial frequencies separated by 1 octave steps. Using a method of adjustment, observers adjusted the retinal disparity of an aperiodic narrow-band stimulus until it appeared in the depth plane defined by two flanking reference lines. Variations in contrast affected stereoacuity (the standard deviation of ten depth settings), with better performance observed at higher contrasts. Data were fit with straight lines (on a log-log plot), indicating a power-law dependence on contrast; the slope was steeper at lower spatial frequencies. These findings are consistent with the idea that disparity is computed from the responses of size-tuned mechanisms characterized by nonlinear contrast transfer functions. In a second experiment, the effects of interocular differences in contrast on stereoacuity were studied for two conditions. In the first condition, one eye always viewed a high-contrast target while the other eye viewed targets of successively lower contrast; in the second condition, one eye always saw a target of near-threshold contrast while the other eye saw targets of successively higher contrast. When the fixed contrast was high, stereoacuity deteriorated steadily as the interocular difference in contrast increased; the loss of stereoacuity was greatest at the lowest spatial frequency. When the fixed contrast was low, however, small increases in the contrast to one eye had no deleterious effect on stereoacuity. Once interocular contrast settings exceeded a certain difference, stereoscopic acuity began to deteriorate at lower spatial frequencies. These results address the issue of the stage of visual processing at which contrast exerts its influence on stereopsis.     

Vernier acuity with opposite-contrast stimuli

Vernier acuity has usually been tested with stimuli of the same contrast polarity (SC). This traditional vernier acuity was compared to that obtained with stimuli of opposite-contrast (OC) in which one target was brighter than the background and the other was darker. For both bar and dot targets vernier acuity with OC stimuli was about half as good as with SC stimuli. There were large individual differences in the size of the disadvantage with OC stimuli, although thresholds remained within the hyperacuity range. There were also individually-differing biases to see a dark vernier stimulus on one or the other side of a bright stimulus. Differences between OC and SC vernier acuities persisted over a wide range of interstimulus spacings, widths, and contrasts. At extremes of these spatial manipulations acuities became similar, but only because SC acuities were degraded to the level of OC acuities. Subjects showed little improvement in OC vernier acuity, even after 50,000 trials. It is concluded that finest judgements of spatial position arise in a level of the visual system at which light and dark stimuli are treated independently.     

Voluntary attention in peripheral vision and its effects on acuity and differential thresholds

The three experiments described in this paper were intended to show whether voluntary attention to a particular part of the peripheral visual field had any effect on the accuracy of the subject's perception. Test objects near to threshold value (for acuity or for changes in luminance) were used. The experiments were also designed to study the possible distracting effect of other stimuli presented simultaneously in different parts of the field.

In Experiment 1 the subject could be given foreknowledge of the position in which an acuity test object would appear. In Experiment 2 the signal of where to attend was given simultaneously with the exposure of an acuity test object. In Experiment 3 differential thresholds for luminance were investigated by methods similar to those used in Experiment 2.

It was found in all these cases that the instructions to attend to a particular part of the peripheral field had no significant effect on perception unless there were simultaneously exposed “competing” stimuli in other parts of the field. The results support the view that, in peripheral vision, attention acts selectively on the immediate memory trace only when there is a complex pattern of stimulation.     

Contrast thresholds for identification of numeric characters in direct and eccentric view

Aubert and Foerster (1857) are frequently cited for having shown that the lower visual acuity of peripheral vision can be compensated for by increasing stimulus size. This result is seemingly consistent with the concept of cortical magnification, and it has been confirmed by many subsequent authors. Yet it is rarely noted that Aubert and Foerster also observed a loss of the "quality of form." We have studied the recognition of numeric characters in foveal and eccentric vision by determining the contrast required for 67% correct identification. At each eccentricity, the lowest contrast threshold is achieved with a specific stimulus size. But the contrast thresholds for these optimal stimuli are not independent of retinal eccentricity as cortical magnification scaling would predict. With high-contrast targets, however, threshold target sizes were consistent with cortical magnification out to 6 degrees eccentricity. Beyond 6 degrees, threshold target sizes were larger than cortical magnification predicted. We also investigated recognition performance in the presence of neighboring characters (crowding phenomenon). Target character size, distance of flanking characters, and precision of focusing of attention all affect recognition. The influence of these parameters is different in the fovea and in the periphery. Our findings confirm Aubert and Foester's original observation of a qualitative difference between foveal and peripheral vision.     

Influence of background on precision of 3D depth judgment tasks in a real environment

Presently, little is known about the effect of curved backgrounds against which the target stimulus is presented on precision in stereoacuity. The experiment analyzed the influence of stimulus orientation and 3D background configuration on stereoscopic vision. Participants were instructed to perform 3D visual alignment tasks on a modified version of the Howard-Dolman apparatus, whereupon precision in depth perception for different curved backgrounds (flat, black, concave, and convex) was evaluated. In addition, the influence of stimulus orientation (0 degrees, 45 degrees, and 90 degrees) on precision was examined. The findings revealed an underestimation in the perceived depth in all background configurations, indicating highest and lowest precision outcomes for convex and concave backgrounds, respectively. In addition, a significant interaction of background and orientation was found. It was concluded that, in a real environment, background local depth cues are integrated with target stimuli to contribute to depth perception.     

The neural correlates of orienting to walking direction in 6‐month‐old infants: An ERP study

The ability to detect social signals represents a first step to enter our social world. Behavioral evidence has demonstrated that 6‐month‐old infants are able to orient their attention toward the position indicated by walking direction, showing faster orienting responses toward stimuli cued by the direction of motion than toward uncued stimuli. The present study investigated the neural mechanisms underpinning this attentional priming effect by using a spatial cueing paradigm and recording EEG (Geodesic System 128 channels) from 6‐month‐old infants. Infants were presented with a central point‐light walker followed by a single peripheral target. The target appeared randomly at a position either congruent or incongruent with the walking direction of the cue. We examined infants' target‐locked event‐related potential (ERP) responses and we used cortical source analysis to explore which brain regions gave rise to the ERP responses. The P1 component and saccade latencies toward the peripheral target were modulated by the congruency between the walking direction of the cue and the position of the target. Infants' saccade latencies were faster in response to targets appearing at congruent spatial locations. The P1 component was larger in response to congruent than to incongruent targets and a similar congruency effect was found with cortical source analysis in the parahippocampal gyrus and the anterior fusiform gyrus. Overall, these findings suggest that a type of biological motion like the one of a vertebrate walking on the legs can trigger covert orienting of attention in 6‐month‐old infants, enabling enhancement of neural activity related to visual processing of potentially relevant information as well as a facilitation of oculomotor responses to stimuli appearing at the attended location.     

From visual acuity to hyperacuity: a 10-year update

Visual acuity, the most basic measure of developing pattern vision in human infants, has been used extensively for detecting anomalies of vision and oculomotor coordination. In the past 10 years much has been learned about the development of two hyperacuities, namely, vernier acuity and stereoacuity. These two acuities become superior to grating acuity after the third month and remain so throughout life. Compared to females, males show slower development of stereopsis and vernier acuity, but not grating acuity, during the third through sixth months. We have suggested that this may result from the neurotrophic effects of the early pulse of testosterone found in males. Measures of vernier acuity have proven effective in detecting meridional amblyopia in older children who had significant astigmatism in the first year and subsequently lost it. The susceptible period for acquiring meridional amblyopia extends from the second half of the first year to at least the end of the second year. Deviations from the typical oblique effect (equal acuity for vertical and horizontal edges; equal, but lower, acuity for left oblique and right oblique) may result from uncorrected astigmatism early in life.     

Vibrotactile localization on the abdomen: effects of place and space

In this study, we explore the conditions for accurate localization of vibrotactile stimuli presented to the abdomen. Tactile orientation systems intended to provide mobility information for people who are blind depend on accurate identification of location of stimuli on the skin, as do systems designed to indicate target positions in space or the status of remotely operated devices to pilots or engineers. The spatial acuity of the skin has been examined for simple touch, but not for the types of vibrating signals used in such devices. The ability to localize vibratory stimuli was examined at sites around the abdomen and found to be a function of separation among loci and, most significantly, of place on the trunk. Neither the structures underlying the skin nor the types of tactor tested appeared to affect localization. Evidence was found for anatomically defined anchor points that provide localization referents that enhance performance even with wide target spacing.     

Interhemispheric visual masking

Backward masking functions were evaluated in a paradigm in which target and masking stimuli were presented to opposite cerebral hemispheres using separate peripheral pathways. Backward masking occurred dichoptically when the target and mask were projected to opposite hemispheres. These findings indicated that some effective masking mechanisms are mediated by interhemispheric interactions independent of retinal phenomena.     

The asymmetry of lateral interference in visual letter identification

Asymmetry of masking refers to the fact that a masking letter placed on the peripheral side of a target in the visual field will interfere more with recognition of the target than will a masking letter placed on the central side of the target. The experiments in this paper show that lateral masking for a pair consisting of a single target and a single mask cannot be entirely explained by processing interference caused by the mask but that masking ]has a component of purely sensory interference. Furthermore, the asymmetry of masking at the sensory level, when all sources of processing interference are eliminated, can be explained in terms of the falloff in acuity from the center to the periphery of the retina. The sensory component of masking is asymmetrical because, with the target at a constant retinal location, the target-plus-mask configuration is, as a whole, more peripherally located with a peripheral mask than a central one, and it is the location of the target-plus-mask configuration that determines performance.     

Differential aversive learning enhances orientation discrimination

A number of recent studies have documented rapid changes in behavioural sensory acuity induced by aversive learning in the olfactory and auditory modalities. The effect of aversive learning on the discrimination of low-level features in the visual system of humans remains unclear. Here, we used a psychophysical staircase procedure to estimate discrimination thresholds for oriented grating stimuli, before and after differential aversive learning. We discovered that when a target grating orientation was conditioned with an aversive loud noise, it subsequently led to an improvement of discrimination acuity in nearly all subjects. However, no such change was observed in a control group conditioned to an orientation shifted by ±90° from the target. Our findings cannot be explained by contextual learning or sensitisation factors. The results converge with those reported in the olfactory modality and provide further evidence that early sensory systems can be rapidly modified by recently experienced reinforcement histories.     

The relationship between eye movements and spatial attention

Most previous studies of the attentional consequences of making saccadic eye movements have used peripheral stimuli to elicit eye movements. It is argued that in the light of evidence showing automatic “capture” of attention by peripheral stimuli, these experiments do not distinguish between attentional effects due to peripheral stimuli and those due to eye movements. In the present study, spatial attention was manipulated by varying the probability that peripheral probe stimuli would appear in different positions, while saccades were directed by a central arrow, enabling the effects of attention and eye movements to be separated. The results showed that the time to react to a peripheral stimulus could be shortened both by advance knowledge of its likely position and, separately, by preparing to make a saccade to that position. When the saccade was directed away from the most likely position of the probe, the targets for attention and eye movements were on opposite sides of the display. In this condition, the effects of preparing to make a saccade proved to be stronger than the effects of attentional allocation until well after the saccade had finished, suggesting that making a saccade necessarily involves the allocation of attention to the target position. The effects of probe stimuli on saccade latencies were also examined: probe stimuli that appeared before the saccade shortened saccade latencies if they appeared at the saccade target, and lengthened saccade latencies if they appeared on the opposite side of fixation. These facilitatory and inhibitory effects were shown to occur at different stages of saccade preparation and suggest that attention plays an important role in the generation of voluntary eye movements. The results of this study indicate that while it is possible to make attention movements without making corresponding eye movements, it is not possible to make an eye movement (in the absence of peripheral stimulation) without making a corresponding shift in the focus of attention.     

Location invariance in masked repetition priming of letters and words

Earlier studies have suggested that information from a prime stimulus can be integrated with target information even when the two stimuli appear at different spatial locations. Here, we examined such location invariance in a masked repetition priming paradigm with single letter and word stimuli. In order to neutralize effects of acuity and spatial attention on prime processing, subliminal prime stimuli always appeared on fixation. Target location varied randomly from trial to trial along the horizontal meridian at one of seven possible locations for letter stimuli (? 7° to + 7°) and three positions for word stimuli (? 4°, 0°, + 4°). Speed of responding to letter and word targets was affected by target location, and by priming, but the size of repetition priming effects did not vary as a function of target location. These results suggest that masked repetition priming is mediated by representations that integrate information about object identity independently of object location.     

Deaf and hearing children: a comparison of peripheral vision development

This study investigated peripheral vision (at least 30° eccentric to fixation) development in profoundly deaf children without cochlear implantation, and compared this to age-matched hearing controls as well as to deaf and hearing adult data. Deaf and hearing children between the ages of 5 and 15 years were assessed using a new, specifically paediatric designed method of static perimetry. The deaf group (N = 25) were 14 females and 11 males, mean age 9.92 years (range 5-15 years). The hearing group (N = 64) were 34 females, 30 males, mean age 9.13 years (range 5-15 years). All participants had good visual acuity in both eyes (< 0.200 LogMAR). Accuracy of detection and reaction time to briefly presented LED stimuli of three light intensities, at eccentricities between 30° and 85° were measured while fixation was maintained to a central target. The study found reduced peripheral vision in deaf children between 5 and 10 years of age. Deaf children (aged 5-10 years) showed slower reaction times to all stimuli and reduced ability to detect and accurately report dim stimuli in the far periphery. Deaf children performed equally to hearing children aged 11-12 years. Deaf adolescents aged 13-15 years demonstrated faster reaction times to all peripheral stimuli in comparison to hearing controls. Adolescent results were consistent with deaf and hearing adult performances wherein deaf adults also showed significantly faster reaction times than hearing controls. Peripheral vision performance on this task was found to reach adult-like levels of maturity in deaf and hearing children, both in reaction time and accuracy of detection at the age of 11-12 years.     

Effects of prime-target spatial separation and attentional deployment on masked repetition priming

In two masked repetition priming experiments with letter stimuli, the positions of prime and target stimuli were varied horizontally from fixation. Priming effects did not interact with position when prime and target location covaried (Experiment 1A) but diminished with increasing prime eccentricity when targets were always centrally located (Experiment 1B). Two accounts of this pattern of priming effects were proposed that postulate two different mechanisms over and above effects of visual acuity. The integration account postulates degree of separation of prime and target stimuli as the critical factor, and the attentional account postulates spatial attention as the critical factor. The results of Experiment 2, in which prime and target positions were manipulated orthogonally, were in favor of the attentional account. Repetition priming did not vary as a function of whether or not primes and targets appeared at the same location, but target processing was facilitated independently of priming when targets appeared at the same location as primes, especially in the right visual field.     

Visual resolution in the periphery

Visual acuity thresholds were determined for two Os with a 3-deg square grating target presented for 0.2 sec within a steadily illuminated surround field matched in luminance to the test field. Measurements were made in the fovea, and at 10, 20, and 30 deg along the horizontal meridian of the temporal retina, at luminances between ?3.5 and 3.0 log mL. The foveal acuity-luminance functions showed a large increase in acuity up to 1 or 2 log mL, but at peripheral locations very little increase occurred above 0 log mL. The maximum acuity reached at photopic luminances dropped sharply with increasing eccentricity. Visual acuities were two to four times higher than those previously reported for the periphery; methodological and target differences are presented to account for this result.     

Asymmetric object substitution masking

Object substitution masking occurs when a lateral mask persists beyond the duration of a target, reflecting reentrant processes in vision (V. Di Lollo, J. Enns, & R. Rensink, 2000). The authors studied whether substitution masking is location specific and whether it is symmetric around the target. A brief circular display of letters was presented along with a mask that designated the target. The mask was centered on the target or 1.1 degrees to the central or to the peripheral side. Substitution masking was found even when the target and the mask were at different locations. It was asymmetric and stronger when the mask was to the peripheral side of the target than to the central side. Asymmetric substitution was observed using various masks. It could not be explained by retina acuity gradients and was not attenuated by focused attention. The authors propose that target selection triggers an asymmetric inhibitory surround that is stronger toward the central side of the target.     

Movement and focused attention: A failure to replicate

Our original goal was to explore the nature of the grouping-by-movement phenomenon reported by Driver and Baylis (1989). In their studies, distractors that moved in common with a centrally located target had a larger influence on focused-attention performance than did more proximate but stationary distractors. These results seemed particularly important since they suggested, contrary to the predictions of space-based models of attention, that attention could be allocated to noncontiguous regions of the visual field. Their results also suggested mandatory processing of stimuli with common motion. Unfortunately, we were unable to replicate this grouping-by-movement effect. In the conditions of Experiment 1 in which we replicated Driver and Baylis’s methodology, stationary distractors produced a larger response-compatibility effect than did the more distant distractors that moved in common with the target. In Experiment 2, we redundantly coded the centrally located target and the far distractors with common movement and color. However, the results were identical to those obtained in Experiment J. The stationary near distractors that appeared in a different color from the target and the far distractors produced the largest response-compatibility effect. In a final experiment, we attempted to compensate for the reduced acuity of the moving distractors by adjusting their size by a cortical magnification factor. However, even with this manipulation, we found a larger response-compatibility effect for the stationary near distractors than for the moving distant distractors. Our results suggest that subjects are capable of selectively processing a target item that moves in common with distractors.     

Movement and focused attention: a failure to replicate.

Our original goal was to explore the nature of the grouping-by-movement phenomenon reported by Driver and Baylis (1989). In their studies, distractors that moved in common with a centrally located target had a larger influence on focused-attention performance than did more proximate but stationary distractors. These results seemed particularly important since they suggested, contrary to the predictions of space-based models of attention, that attention could be allocated to noncontiguous regions of the visual field. Their results also suggested mandatory processing of stimuli with common motion. Unfortunately, we were unable to replicate this grouping-by-movement effect. In the conditions of Experiment 1 in which we replicated Driver and Baylis's methodology, stationary distractors produced a larger response-compatibility effect than did the more distant distractors that moved in common with the target. In Experiment 2, we redundantly coded the centrally located target and the far distractors with common movement and color. However, the results were identical to those obtained in Experiment 1. The stationary near distractors that appeared in a different color from the target and the far distractors produced the largest response-compatibility effect. In a final experiment, we attempted to compensate for the reduced acuity of the moving distractors by adjusting their size by a cortical magnification factor. However, even with this manipulation, we found a larger response-compatibility effect for the stationary near distractors than for the moving distant distractors. Our results suggest that subjects are capable of selectively processing a target item that moves in common with distractors.