Binocular vision enhances phase discrimination by filtering the background

Previous studies have shown that the detectability of a noise-masked target can be enhanced under stereoscopic viewing when the target’s interocular disparity differs from that of the noise. This enhanced detectability can be accounted for by a model postulating that the binocular system linearly sums the left-eye and right-eye views of a visual scene. This model also predicts enhanced phase discrimination under specifiable interocular disparities of target and noise. Two experiments were conducted in which subjects were asked to discriminate between two luminance patterns (target and foil) that differed only in phase. The target patterns were constructed by summating two vertical sinusoidal gratings in which the phase difference between the higher and the lower spatial frequency gratings was 45°. The foils contained the same two component frequencies, with a phase difference of ?45°. Thus, targets and foils were mirror images of one another. The ability of subjects to Discriminate between these stereoscopically viewed mirror-image patterns was investigated under two sets of interocular disparities: those that, according to our model, would unmask one or both spatial frequency components, and those that would leave both components masked by the noise. Phase discrimination was enhanced only when both component frequencies of the target and foil were unmasked. The implications of these findings for template-matching and phase-discrimination models of pattern discrimination are considered.     

Binocular single vision achieved by fusion and suppression

The occurrences of fusion and suppression were determined from stereograms which produced two retinal images located at equal distances but in opposite directions from the fovea. Subjects reported whether the dichoptic stimulus appeared single or not, and if single whether it appeared in the center of the visual field. The report of centrality is predicted by the fusion theory of single vision and that of noncentrality by the suppression theory. Experiment 1, with eight subjects, showed that for small disparities perceived singleness was the percept predicted by the fusion theory; for larger disparities, the percepts could sometimes be predicted by the fusion theory and other times by the suppression theory. Experiment 2, with 16 subjects, showed that with larger stimuli the percept predicted by the fusion theory is more likely to occur. Experiment 3, with four subjects, showed that the centrality was reported when the stimuli were presented for 100 msec. This result provided support for our interpretation that the centrality reports in Experiments 1 and 2 were not due to fixation error and suppression.     

Binocular vision enhances a rapidly evolving affordance priming effect: Behavioural and TMS evidence

Extensive research has suggested that simply viewing an object can automatically prime compatible actions for object manipulation, known as affordances. Here we explored the generation of covert motor plans afforded by real objects with precision (‘pinchable’) or whole-hand/power (‘graspable’) grip significance under different types of vision. In Experiment 1, participants viewed real object primes either monocularly or binocularly and responded to orthogonal auditory stimuli by making precision or power grips. Pinchable primes facilitated congruent precision grip responses relative to incongruent power grips, and vice versa for graspable primes, but only in the binocular vision condition. To examine the temporal evolution of the binocular affordance effect, participants in Experiment 2 always viewed the objects binocularly but made no responses, instead receiving a transcranial magnetic stimulation pulse over their primary motor cortex at three different times (150, 300, 450 ms) after prime onset. Motor evoked potentials (MEPs) recorded from a pinching muscle were selectively increased when subjects were primed with a pinchable object, whereas MEPs from a muscle associated with power grips were increased when viewing graspable stimuli. This interaction was obtained both 300 and 450 ms (but not 150 ms) after the visual onset of the prime, characterising for the first time the rapid development of binocular grip-specific affordances predicted by functional accounts of the affordance effect.     

Binocular vision enhances a rapidly evolving affordance priming effect: Behavioural and TMS evidence

Extensive research has suggested that simply viewing an object can automatically prime compatible actions for object manipulation, known as affordances. Here we explored the generation of covert motor plans afforded by real objects with precision (‘pinchable’) or whole-hand/power (‘graspable’) grip significance under different types of vision. In Experiment 1, participants viewed real object primes either monocularly or binocularly and responded to orthogonal auditory stimuli by making precision or power grips. Pinchable primes facilitated congruent precision grip responses relative to incongruent power grips, and vice versa for graspable primes, but only in the binocular vision condition. To examine the temporal evolution of the binocular affordance effect, participants in Experiment 2 always viewed the objects binocularly but made no responses, instead receiving a transcranial magnetic stimulation pulse over their primary motor cortex at three different times (150, 300, 450 ms) after prime onset. Motor evoked potentials (MEPs) recorded from a pinching muscle were selectively increased when subjects were primed with a pinchable object, whereas MEPs from a muscle associated with power grips were increased when viewing graspable stimuli. This interaction was obtained both 300 and 450 ms (but not 150 ms) after the visual onset of the prime, characterising for the first time the rapid development of binocular grip-specific affordances predicted by functional accounts of the affordance effect.     

Right-hemisphere superiority in the discrimination of spatial phase

Visual field differences have been investigated in various detection and discrimination tasks for simple sinusoidal gratings or for complex gratings composed of two sinusoids of spatial frequencies f and 3f. Sinusoidal gratings were employed to evaluate contrast sensitivity, subthreshold summation effects, aftereffects of adaptation to a high-contrast grating, and spatial-frequency discrimination. The tasks with complex gratings were detection of the 3f component in the presence of a high-contrast f component and spatial-phase discrimination. The stimuli were presented either in the left or in the right visual hemifield. The results indicate a lack of lateralization for detection and spatial-frequency discrimination of sinusoidal gratings, and for the bandwidth of subthreshold summation effects and adaptation aftereffects, whereas the detection of the 3f component in the presence of a high-contrast f component, as well as spatial-phase discrimination of f +3f gratings, show a left-field advantage. This suggests a right-hemisphere superiority in the processing of spatial phase.     

Binocular fixation in the newborn baby.

Three experiments are reported in which the newborn baby's ability to fixate binocularly was investigated, using the corneal reflection technique for measuring eye fixation position. Two criteria for consistent binocular fixation were assessed. These are (1) the two eyes will be optically more divergent when fixating more distant targets, and (2) each eye will be scored as being on-target when corrections for the expected deviations of the pupil center from the fixated stimulus are introduced.In the first experiment vertical arrays of lights were separately shown at distances of 10 and 20 in. from the subjects' eyes (with the retinal image size and luminance of the stimuli held constant). The 12 newborns who gave results at both viewing distances reliably converged to both stimuli, the optical divergence of the pupil centers of the eyes increasing with presentation of the more distant stimulus. In Expt 2 similar stimuli at 5 and 10 in. from the eyes were shown. It was again the case that the subjects reliably converged to the stimulus at 10 in. This was no so for the stimulus at 5 in., and many subjects fixated this stimulus with monocular vision. The failure to converge is probably due to an inability to accommodate to this near distance. In Expt 3 different stimuli (a vertical strip of light, an outline triangle and square, and an array of squares) were presented a constant distance (10 ± 1 in.) from the eyes. The majority of the 15 subjects binocularly fixated all three stimuli: for those subjects who failed to converge consistently to these stimuli the observed alternatives to binocular fixation were monocular fixation, divergent strabismus, and a third category of response that is most probably an indication of inattention to the stimulus. It can be concluded that the newborn baby possesses the ability to fixate binocularly an appropriately presented stimulus, and has the basic requirements for binocular vision.     

Binocular depth perception in the pigeon.

By means of a discrete-trial simultaneous discrimination procedure, pigeons were trained to respond differentially to visual arrays that were identical except that one of them contained a circle displaced in depth when viewed stereoscopically. Performance was severely disrupted when one eye was occluded. The monocular deficit was peculiar to the depth task, inasmuch as no such decrement was seen on a pattern discrimination. The results imply that presence of the displaced circle was discriminated on the basis of a binocular cue. It was also found that pigeons could discriminate the direction of the displacement. Discrimination of depth was independent of the global form and still occurred when elements of the array were randomly displaced in depth. Performance was not disrupted when the absolute convergence angle of the depth stimulus was changed. The cue that consistently accounted for the behavior seen was the detection of the relative angles of convergence--that is, the retinal disparity of the two planes in depth. Thus, despite the lateral position of the eyes of the pigeon, a small binocular field mediates the binocular discrimination of near objects in depth.     

Phenomenal background frequency and the concreteness/imagery effect in verbal discrimination learning

College students gave frequency ratings for concrete and abstract words which were equated on normative frequency. The results replicated the finding of Galbraith and Underwood (1973) that abstract words are perceived to be higher in frequency than concrete words. Different subjects then learned verbal discrimination lists consisting of both abstract and concrete pairs. While the usual concreteness effect was obtained when abstract and concrete items differed widely on phenomenal frequency, it disappeared when these items were equated on perceived frequency. The finding that appropriate frequency manipulations can eliminate the concreteness/imagery effect, coupled with similar findings for other stimulus characteristics, lends strong support to the frequency theory of discrimination learning.     

Bias of phencyclidine discrimination by the schedule of reinforcement.

Pigeons, trained to discriminate phencyclidine from saline under a procedure requiring the bird to track the location of a color, received cumulative doses of phencyclidine, pentobarbital, or d-amphetamine with a variety of schedules of reinforcement in effect (across phases). When the same second-order schedules were used to reinforce responding after either saline or phencyclidine administration, stimulus control by phencyclidine did not depend on the schedule parameter. When different second-order schedules were used that biased responding toward the phencyclidine-correlated key color, pigeons responded on the phencyclidine-correlated key at lower doses of phencyclidine and pentobarbital than when the second-order schedule biased responding toward the saline key color. A similar but less marked effect was obtained with d-amphetamine. Attempts to produce bias by changing reinforcement magnitude (duration of food availability) were less successful. A signal-detection analysis of dose-effect curves for phencyclidine under two of the second-order schedules employed suggested that at low doses of phencyclidine, response bias is a major determinant of responding. As doses were increased, position preferences occurred and response bias decreased; at higher doses both response bias and position preference decreased and discriminability increased. With low doses of pentobarbital, responding again was biased but increasing doses produced position preference with only small increases in discriminability. At low doses of d-amphetamine responding also was biased, but bias did not decrease consistently with dose nor did discriminability increase. These experiments suggest that the schedule of reinforcement can be used to bias responding toward or away from making the drug-correlated response in drug discrimination experiments, and that signal-detection analysis and analysis of responding at a position can be used to separate the discriminability of the drug state from other effects of the drug on responding.     

Reformulation in the phase plane enhances smoothness rater accuracy in stroke

To improve the characterization of motor impairment, we compared the sensitivities of a phase plane metric with temporal domain measures derived from integrated squared jerk (ISJ). Five subjects with stroke and a cohort of 21 neurologically intact volunteers performed self-paced, isolated elbow flexions. Analysis of angular trajectories from the stroke group revealed that temporal domain metrics failed to detect a performance deficit at the p < .05 level, while the phase plane metric did resolve a deficit (p < .01). When applied to a subset of movements with arrest periods, the phase measure also uniquely identified impairment (Wilcoxon rank-sum test, p < .001). Finally, when tested on a data-driven model, the phase measure, but not temporal metrics, increased monotonically with the severity of trajectory distortions. We conclude that motion smoothness can be accurately measured in the phase plane.     

Pattern discrimination in the near-ultraviolet by pigeons

Four pigeons were tested, using an operant conditioning method with successive stimulus presentation, on a pattern discrimination task to determine whether or not they could distinguish patterns that were illuminated by near-ultraviolet (UV) light. Tests at red, green, and UV wavelengths showed that they could significantly discriminate not only the chromatic stimuli that were visible to human observers but also the UV-illuminated patterns that humans could not see. In control sessions, the birds’ performance deteriorated to chance levels when these UV wavelengths were blocked by additional filters. Their discrimination of UV patterns precludes that the pigeon’s known sensitivity to UV is mediated by a preretinal fluorescence, as is probably the case in some other animals, since such a fluorescence does not permit a focused retinal image. Possible retinal mechanisms mediating their UV detection are discussed.     

Pattern vision of the honeybee (Apis mellifera): blue and green receptors in the discrimination of translocation

The visual discrimination of horizontal gratings by the honeybee (Apis mellifera) was studied in a Y-choice apparatus with fixed patterns presented vertically at a set range. Translocation in this context is the exchange of the positions of two different colored or black areas. This paper investigates what cues the bees have learned in this task. The patterns, made from combinations of calibrated colored papers, are designed to explore the parts played by the blue and green receptors when the boundary between the two colors provides contrast to only one receptor type. Horizontal translocation is not discriminated without contrast to the green receptors, but up/down translocation can be discriminated whatever the contrast at the boundary. The trained bees were tested on the same patterns made with different papers that included extreme changes in contrast. The results show that discrimination of up/down translocation involves green receptors and also blue receptors. When bees discriminate a translocation that shows contrast to only one type of receptor, they do not use the apparent brightness or the direction of the contrast to that receptor type acting alone. Instead, they discriminate the locations of colored areas irrespective of intensity differences or directions of contrasts. They use some measure of the photon flux at both receptor types and remember the difference between the colors and their locations.     

Covert discrimination against gay men by U.S. college students.

This study examined the use of sexual orientation as a meaningful social category and the consequences of using this category. The sample consisted of 260 U.S. college students who viewed a video and completed a 29-item scale (L. L. Thompson & J. Crocker, 1990) and the 7-item Homophobia Scale (R. A. Bouton et al., 1987). Results showed that participants' adjective ratings of targets favored gay men. Participants did not exhibit greater bias toward gay men when provided with justification. However, there was a pattern of bias in which participants showed favoritism toward heterosexual male targets when provided with no justification for bias.     

Controlling relations in conditional discrimination and matching by exclusion.

Normally capable adults learned two-choice identity matching of three-digit numerals and arbitrary matching of physically dissimilar nonsense syllables. The stimuli were displayed on a computer terminal, and responses consisted of typing on the terminal's keyboard. In Experiment 1, every trial displayed a sample numeral, a comparison numeral, and three equal signs (= = =). The comparison stimulus was to be selected if it was identical with the sample; otherwise the equal sign was to be selected. This "single comparison" method was then used to show that arbitrary matching could be based upon either sample-S+ or sample-S- relations. In Experiment 2, a series of probe trials displayed a novel sample, a comparison stimulus from the arbitrary matching baseline, and = = =. Subjects typically selected = = =; they apparently were excluding the baseline comparison stimulus. Experiments 3 through 5 investigated which variables in training would lead to the selection of baseline comparison stimuli in response to novel samples. Behavior was usually unchanged when baseline training included relating comparison stimuli to as many as four different samples. Punishment contingencies were effective, but performance did not generalize unless those contingencies were applied in relation to more than one baseline comparison stimulus.     

Visual discrimination of shape by octopus. squares and triangles

An experiment was performed upon visual discrimination of shape by the octopus in order to test two predictions derived from a theory of visual discrimination of orientation and shape. Two groups of octopuses were trained to discriminate between a square and a triangle and between a diamond and a triangle. It was found that octopuses discriminate more readily between a square with base horizontal and a triangle than between a diamond and a triangle. Transfer tests showed that: (1) For the octopus, an upright and an inverted triangle have more equivalence than a diamond and a square with base horizontal. (2) Octopuses do not discriminate between the figures used by analysing only differences in one part of the figures (e.g. bases or tops). (3) Having learned the initial discrimination, octopuses transfer to both larger and smaller figures. (4) A pentagon has more equivalence to a square or diamond than to a triangle. (5) A circle is not treated as equivalent to a square. The results are taken to be in agreement with the theory that octopuses analyse the vertical and lateral extents of figures, and that shape discrimination is achieved by analysing the changes in the rates of change in the firing of neurons representing the vertical and lateral extents of the shapes. The results are shown to differ from those obtained with birds and rats, but to agree with results found for higher mammals where these are available for comparison.     

Parallel discrimination of subjective contours defined by offset gratings.

Recent physiological studies (von der Heydt & Peterhans, 1989) suggest that the orientation of subjective contours is encoded very early in the visual system (V2 in monkey). This result is seemingly at odds with existing psychophysical data which suggest that the detection of subjective contours involves selective attention. It is argued that certain subjective contours are registered in a reflexive (bottom-up) manner by the visual system but that selective attention may be needed to gain access to this representation. To assess this suggestion, a visual-search task was used in which subjects were to detect the presence of a horizontal (vertical) subjective contour (defined by offset gratings) in a variable number of vertical (horizontal) subjective contours (also defined by offset gratings). When there were no competing organizations within the display, detection was indeed independent of the number of nontarget distractors, that is, selective attention was unnecessary. In a second experiment, we found that a curved form (a crescent defined by subjective contours) was easier to detect in a background of vertical bars (also defined by subjective contours) than vice versa, namely, a search asymmetry paralleling those found by Treisman and Gormican (1988). A final experiment showed that when the horizontal and vertical bars of the first experiment formed textured regions, they could be discriminated at very brief display durations (30-120 msec). However, when the line terminations aligned along the subjective contour were tapered rather than abrupt, discrimination dropped off with the degree of tapering. The latter result is consistent with the assumption that the registration of subjective contours in V2 involves the integration of responses from aligned, end-stopped cells found in V1 (von der Heydt & Peterhans, 1989).