Role of chromaticity, contrast, and local orientation cues in the perception of density

We compared the role of the red-green, blue-yellow, and luminance post-receptoral mechanisms in the perception of density. The task requires the comparison of densities between two stimuli composed of oriented bandpass elements, pseudo-randomly scattered across an area of constant size. The perception of density differences was measured by a temporal 2AFC procedure for all pairs of mechanisms and for four possible densities. We found that stimuli of identical physical densities are not perceived equally: there is a consistent bias in favour of blue-yellow stimuli which are perceived as significantly more dense than red-green and achromatic stimuli. We considered three factors that could have differentially affected the density perception of blue-yellow stimuli: an increase in the perceived size of the individual blue-yellow elements, a perceived contrast difference, and the presence of local orientation cues. We found that the increased perceived density of the blue-yellow stimuli occurred despite the fact that there was no increase in perceived size of the individual elements, and remained despite corrections for the two other factors. We conclude that the significant increase in perceived density for the blue-yellow mechanism is a global effect, associated with a perceived colour 'melting' of the elements in the array. Our data were fitted with the occupancy model of Allik and Tuulmets (1991, Perception & Psychophysics 49 303-314) and we found that blue-yellow stimuli have a greater 'occupancy' than red-green or achromatic stimuli.     

Judgments of path, not heading, guide locomotion

To steer a course through the world, people are almost entirely dependent on visual information, of which a key component is optic flow. In many models of locomotion, heading is described as the fundamental control variable; however, it has also been shown that fixating points along or near one's future path could be the basis of an efficient control solution. Here, the authors aim to establish how well observers can pinpoint instantaneous heading and path, by measuring their accuracy when looking at these features while traveling along straight and curved paths. The results showed that observers could identify both heading and path accurately (approximately 3 degrees ) when traveling along straight paths, but on curved paths they were more accurate at identifying a point on their future path (approximately 5 degrees ) than indicating their instantaneous heading (approximately 13 degrees ). Furthermore, whereas participants could track changes in the tightness of their path, they were unable to accurately track the rate of change of heading. In light of these results, the authors suggest it is unlikely that heading is primarily used by the visual system to support active steering.     

TIMING AND APPARENT MOTION PATH CHOICE WITH HUMAN BODY PHOTOGRAPHS

Abstract— In demonstrations of apparent motion, observers typically report seeing motion along the shortest possible path between two sequentially presented objects. Recent work has demonstrated that violations of this shortest path rule occur with realistic photographs of a human body displayed for sufficiently long temporal intervals when a longer path is more anatomically plausible than the shortest path. The current set of experiments investigated the mechanisms by which information about biomechanical motion constrains apparent motion perception. In Experiment 1, we demonstrated, first, that the availability of extra processing time does not simply—in and of itself—result in the perception of longer paths of apparent motion. Second, we rejected the hypothesis that the perception of biomechanically correct paths of apparent motion depends on biologically appropriate velocities. In Experiment 2, we discovered that the longer the motion path required to satisfy the biomechanical movement limitations of the stimulus, the longer the time needed to construct and therefore perceive that path. These findings together suggest that additional processing time is necessary, but not sufficient, for interpolations of longer paths.     

Curved movement paths and the Hering illusion: Positions or directions?

When trying to move in a straight line to a target, participants produce movement paths that are slightly (but systematically) curved. Is this because perceived space is curved, or because the direction to the target is systematically misjudged? We used a simple model to investigate whether continuous use of an incorrect judgement of the direction to the target could explain the curvature. The model predicted the asymmetries that were found experimentally when moving across a background of radiating lines (the Hering illusion). The magnitude of the curvature in participants' movements was correlated with their sensitivity to the illusion when judging a moving dot's path, but not with their sensitivity when judging the straightness of a line. We conclude that a misjudgement of direction causes participants to perceive a straight path of a moving dot as curved and to produce curved movement paths.     

Brightness contrast: a reinterpretation of compound cue and combined cue experiments with pigeons.

A group of three pigeons was trained on a 4-ply multiple schedule: a green color and a vertical line superimposed upon an achromatic background as positive stimuli, and a red color and a horizontal line on an achromatic background as negative stimuli. The pigeons were tested with the vertical line superimposed upon different achromatic background intensities, then with the vertical line superimposed upon different green background intensities, and finally with the vertical line and its training achromatic backgfound attenuated (and unattenuated) by a neutral density filter. The gradients peaked at the luminance of the achromatic background used during training and at the equivalent luminance for the green background when it was substituted for the achromatic background. The brightness contrast, not the background luminance, was the critical variable as the neutral density filter attenuated both the line and the background equally, leaving brightness contrast unchanged; there was no response decrement to this attenuated stimulus. Two other groups of three pigeons showed that they attended to line orientation as well as to brightness contrast. The brightness contrast hypothesis was extended to explain results of attention experiments and combined cue experiments which have used line stimuli in combinations with different backgrounds.     

Objects in the path of apparent motion

Experiments by several investigators suggest that forms between inducing stimuli for apparent motion may deflect motion from a straight path. In an experiment in which a binocularly viewed object was sometimes positioned between the inducing dots, we discovered that the degree of curvature of the path that is most likely to be reported depends upon the interstimulus interval whether or not the space between inducing dots contains an object. The interstimulus interval at which motion is most frequently reported is longer for curved paths of motion than for linear paths even though the spatial separation of inducing stimuli is held constant. The results suggest that apparent motion in depth is not based upon form.     

Color correspondence in apparent motion

To maintain figural identity during motion perception, the visual system must match images over space and time. Correct matching requires a metric for identifying "corresponding" images, those representing the same physical object. To test whether matching is based on achromatic (black/white) polarity and chromatic (red/green) color, observers viewed an ambiguous motion display and judged the path of apparent motion. Matching preserved black/white identity regardless of whether frames were viewed binocularly or dichoptically. Red/green identity was also preserved, but coherence of motion depended in part on the number of frames in the motion sequence and on the background luminance. These results suggest that correspondence is computed by a weighted metric containing terms for image features coded early in visual processing.     

Delayed detection of tonal targets in background noise in dyslexia

Individuals with developmental dyslexia are often impaired in their ability to process certain linguistic and even basic non-linguistic auditory signals. Recent investigations report conflicting findings regarding impaired low-level binaural detection mechanisms associated with dyslexia. Binaural impairment has been hypothesized to stem from a general low-level processing disorder for temporally fine sensory stimuli. Here we use a new behavioral paradigm to address this issue. We compared the response times of dyslexic listeners and their matched controls in a tone-in-noise detection task. The tonal signals were either Huggins Pitch (HP), a stimulus requiring binaural processing to elicit a pitch percept, or a pure tone-perceptually similar but physically very different signals. The results showed no difference between the two groups specific to the processing of HP and thus no evidence for a binaural impairment in dyslexia. However, dyslexic subjects exhibited a general difficulty in extracting tonal objects from background noise, manifested by a globally delayed detection speed.     

Response rate, reinforcement frequency, and behavioral contrast

Pigeons responded for food on a multiple schedule in which periods of green-key illumination alternated with periods of red-key illumination. When behavior had stabilized with a variable-interval 2-min schedule of reinforcement operating during both stimuli, low rates of responding (interresponse times greater than 2 sec) were differentially reinforced during the green component. Conditions during the red stimulus were unchanged. Response rates during the green component fell without changing the frequency of reinforcement but there were no unequivocal contrast effects during the red stimulus. The frequency of reinforcement during the green component was then reduced by changing to a variable-interval 8-min schedule without reducing the response rates in that component, which were held at a low level by the spacing requirement. Again, the conditions during the red stimulus were unchanged but response rates during that stimulus increased. These results show that reductions in reinforcement frequency, independently of response rate, can produce interactions in multiple schedules.     

Right hemisphere specialization for color detection

Three experiments were carried out to investigate hemispheric asymmetry in color processing among normal participants. In Experiment 1, it was shown that the reaction times (RTs) of the dominant and non-dominant hands assessed using a visual target presented at the central visual field, were not significantly different. In Experiment 2, RTs of ipsilateral hands to lateralized chromatic stimuli revealed that the processing time was 17 ms shorter in the right hemisphere (RH) than that in the left hemisphere among the right-handed participants, whereas no significant difference was found among the left-handed participants. On the other hand, RTs to lateralized achromatic stimuli showed no such asymmetry among both the right- and left-handed participants (Experiment 3). These findings strongly suggest RH superiority for detection of color among right-handed individuals.     

Preattentive processing or prefocal processing?

The concept of preattentive processing is analyzed and alternative views of it are presented. A basic question is whether processing required for preattentive input selection is qualitatively different from post-selection processing. In order to study this, subjects were presented in one set of conditions with one stimulus at either of two locations, and in another set of conditions, simultaneously with two stimuli. The stimuli could be green or red, or large or small. Subjects were asked to indicate the location (or the color, or the size) of the single stimulus in the single-stimulus conditions, or of a predesignated stimulus (say, the red one) in the dual-stimulus conditions. Responses were generally slower in the dual-stimulus conditions. The increases in reaction time were accounted for by the times it takes to process for response selection the properties by which the target stimulus could be selected, as indicated by the results of two control conditions. The results as well as some other considerations do not support the view that preattentive processing is necessarily of a type that qualitatively differs from post-selection processing.     

Categorical and coordinate spatial processing: more on contributions of the transient/magnocellular visual system

Observers were presented with stimuli consisting of a line and two horizontally separated dots. A categorical spatial task required observers to indicate whether the dots were above or below the line and a coordinate spatial task required observers to indicate whether the line could fit into the space between the two dots. Coordinate (but not categorical) spatial processing was less accurate and took longer with stimuli presented on a red background than with stimuli presented on a green background, even though the background color varied randomly from trial to trial and the viewing screen remained gray between trials. Because the color red attenuates processing in the transient/magnocellular visual system, these results suggest that coordinate spatial processing is dependent on that pathway. Furthermore, such effects do not involve mechanisms of perceptual adaptation that depend on the same color background being present throughout an experiment or for a prolonged period of time. As in earlier experiments, the effects of color condition were the same regardless of which visual field (and hemisphere) received the stimulus information. However, in contrast to the results of earlier experiments, there was no significant interaction of task and visual field.     

Planned Straight or Biased to Be So? The Influence of Visual Feedback on Reaching Movements

Abstract

Behavioral studies consistently find that subjects move their hand along straight paths despite considerations that suggest reaches should be curved. Literature on this topic makes it clear that the experimentally displayed feedback influences how subjects reach. Could the standard visual feedback, a displayed cursor, explain the lack of path curvature in experimental results? To address this question, we conducted three experiments to examine reach behavior in the absence of the standard visual feedback. In the first experiment, we found significant increases in curvature as visual feedback was progressively extinguished across groups. A second experiment revealed that practiced reaches became curved after the standard visual feedback was removed. A final experiment found that subjects’ reaches made before and after a brief display of visual feedback were similar, indicating a preference for specific curved trajectories. Our results suggest that the consistently straight reaches often observed could be due to a bias to move the displayed cursor straight, which when removed reveal subject-specific preferences for reaches that are often curved.     

Objects of attention, objects of perception

Four experiments were conducted, to explore the notion of objects in perception. Taking as a starting point the effects of display content on rapid attention transfer and manipulating curvature, closure, and processing time, a link between objects of attention and objects of perception is proposed. In Experiment 1, a number of parallel, equally spaced, straight lines facilitated attention transfer along the lines, relative to transfer across the lines. In Experiment 2, with curved, closed-contour shapes, no "same-object" facilitation was observed. However, when a longer time interval was provided, in Experiment 3, a same-object advantage started to emerge. In Experiment 4, using the same curved shapes but in a non-speeded distance estimation task, a strong effect of objects was observed. It is argued that attention transfer is facilitated by line tracing but that line tracing is encouraged by objects.     

The cost of simplifying complex developmental phenomena: a new perspective on learning to walk

Researchers can study complex developmental phenomena with all the inherent noise and complexity or simplify behaviors to hone in on the essential aspects of a phenomenon. We used the development of walking as a model system to compare the costs and benefits of simplifying a complex, noisy behavior. Traditionally, researchers simplify infant walking by recording gait measures as infants take continuous, forward steps along straight paths. Here, we compared the traditional straight‐path task with spontaneous walking during 20 minutes of free play in 97 infants (10.75–19.99 months of age). We recorded infants’ footfalls on an instrumented floor to calculate gait measures in the straight‐path and free‐play tasks. In addition, we scored videos for other critical aspects of spontaneous walking—steps per bout, shape of walking path, and step direction. Studying infant walking during free play incurred no cost compared with the straight‐path task, but considerable benefits. Straight‐path gait was highly correlated with spontaneous gait and both sets of measures improved with walking age, validating use of the straight‐path task as an index of development. However, a large proportion of free‐play bouts were too short to permit standard gait measures, and most bouts were curved with omnidirectional steps. The high prevalence of these “non‐canonical” bouts was constant over development. We propose that a focus on spontaneous walking, the phenomenon we ostensibly wish to explain, yields important insights into the problems infants solve while learning to walk. Other areas of developmental research may also benefit from retaining the complexity of complex phenomena.     

Curvature affects haptic length perception

One possible way of haptically perceiving length is to trace a path with one’s index finger and estimate the distance traversed. Here, we present an experiment in which observers judge the lengths of paths across cylindrically curved surfaces. We found that convex and concave surfaces had qualitatively different effects: convex lengths were overestimated, whereas concave lengths were underestimated. In addition, we observed that the index finger moved more slowly across the convex surface than across the concave one. As a result, movement times for convex lengths were longer. The considerable correlation between movement times and length estimates suggests that observers take the duration of movement as their primary measure of perceived length, but disregard movement speeds. Several mechanisms that could underlie observers’ failure to account for speed differences are considered.     

COLOR SPACE OF NORMALLY SIGHTED AND COLOR-DEFICIENT OBSERVERS RECONSTRUCTED FROM COLOR NAMING

Abstract— An experimental procedure based an the color-naming method introduced by Boynton, Schafer, and Neun (1964) was used to study the color appearance of equilumtnant spectral stimuli in observers with congenital red-green color deficiencies, as well as in normal trichromats. Subjects' responses (choice of one or more labels from the set red, yellow, green, blue, and white) were converted to numeric scores, which were used to estimate subjective difference between pairs of colors Individual subjects' matrices were processed by means of multidimensional scaling. As in the direct rating of color dissimilarities in normal trichromats. (Sokolov & Izmatlov, 1983), and color-deficient observers (Paramei Izmailov, & Sokolov, 1991), these indirectly obtained measures yielded a color space in which three dimensions appear to be necessary and sufficient. The dimensions are interpreted as evidence for red-green, Mae-yellow, and achromatic (saturation) sub-systems. Based on the color-naming technique, three-dimensional spaces were reconstructed for the color-deficient observers. These results were compared with those obtained by Helm (1964). It is argued that retaining more than one (blue-yellow) dimension in the color spaces of such observers provider additional information indicating preservation of residual red-green discrimination accompanied by finer discrimination of chroma than in normal trichromats. The spherical model of color discrimination developed for normal trichromats (lzmailov & Sokolov, 1991) is shown to be valid for color-deficient subjects as well and may be useful as a framework for differentiating proton and deutan types of color deficiency. Color-naming functions, which seem not to reveal a differentiation between protans and deutans, provide results form which this differentiation can be extracted in reconstructed color spaces.     

A ratio principle for a red/green and a yellow/blue channel?

There is strong empirical evidence that, under adaptation to another achromatic color stimulus, the lightness of an achromatic color stimulus depends on the ratio of the luminances of the two stimuli. In the present study, the suitability of this ratio principle is tested for two chromatic postreceptoral opponent channels. A Hering red/green channel and a non-Hering yellow/blue channel are specified as chromatic channels. The yellow/blue channel is defined by extrapolating the plane corresponding to unique green-white linearly to the reddish part of color space, using the plane’s surface as the channel’s equilibria. The experiment was run on an isoluminant plane, measured individually for each observer. Moving along an observer’s measured opponent axes, eight adaptation stimuli were selected for each channel and spanned the whole range of the channel’s coordinates. Red/green equilibria or yellow/blue equilibria were measured as excursions along the adaptation axes. For both presumed channels, the ratios of the equilibrium coordinates of test and adaptation stimuli were essentially constant. This supports the principle’s suitability. However, small asymmetries were found with respect to each channel’s opponent hues. The status of the proposed yellow/blue channel is discussed, as are conditions that might have favored the present findings.     

Prospective versus retrospective coding of samples of stimuli,responses, and reinforcers in delayed matching with pigeons

Pigeons' performance with samples of stimuli (red and green), number of responses (1 and 20), and reinforcers (food and no food) was assessed in a matching-to-sample preparation. Samples of red, 20 responses, and food were each associated with the red comparison stimulus; samples of green, 1 response, and no food were each associated with the green comparison stimulus. Interest focused on whether physically different samples associated with the same comparison stimulus each establish a unique memorial representation embodying the physical attributes of the sample (retrospective coding), or whether they activate a unitary memorial representation embodying an instruction for test responding (prospective coding). In the first experiment, accuracy of choice responding was independent of whether successive sample presentations within a trial involved the same physical sample or physically different but associatively identical samples. A second experiment revealed that, in contrast to other matching preparations, accuracy was not reduced when sample elements were compounded during presentation. It was concluded that physically different samples which are associated with the same comparison stimulus are coded prospectively in terms of an instruction for choice responding.