Biomedical subjects

D Purves

Publications and source records attributed to D Purves.

At least 19 recordsLinked to original sources

PubMed2000

An empirical explanation of color contrast.

For reasons not well understood, the color of a surface can appear quite different when placed in different chromatic surrounds. Here we explore the possibility that these color contrast effects are generated according to what the same or similar stimuli have turned out to signify in the past about the physical relationships between reflectance, illumination, and the spectral returns they produce. This hypothesis was evaluated by (i) comparing the physical relationships of reflectances, illuminants, and spectral returns with the perceptual phenomenology of color contrast and (ii) testing whether perceptions of color contrast are predictably changed by altering the probabilities of the possible sources of the stimulus. The results we describe are consistent with a wholly empirical explanation of color contrast effects.

Color Perception↗

PubMed2000

Why are angles misperceived?

Although it has long been apparent that observers tend to overestimate the magnitude of acute angles and underestimate obtuse ones, there is no consensus about why such distortions are seen. Geometrical modeling combined with psychophysical testing of human subjects indicates that these misperceptions are the result of an empirical strategy that resolves the inherent ambiguity of angular stimuli by generating percepts of the past significance of the stimulus rather than the geometry of its retinal projection.

Female↗

PubMed2000

The relevance of visual perception to cortical evolution and development.

The quality of brightness--perhaps the simplest visual attribute we perceive--appears to be determined probabilistically. In this empirical conception of the perception of light, the stimulus-induced activity of visual cortical neurons does not encode the retinal image or the properties of the stimulus per se, but associations (percepts) determined by the relative probabilities of the possible sources of the stimulus. If this theory is correct, the rationale for the prolonged postnatal construction of visual circuitry--and the evolution of this visual scheme--is to strengthen and/or create by activity-dependent feedback the empirically determined association on which vision depends.

Animals↗

PubMed2000

Color vision and the four-color-map problem.

Four different colors are needed to make maps that avoid adjacent countries of the same color. Because the retinal image is two dimensional, like a map, four dimensions of chromatic experience would also be needed to optimally distinguish regions returning spectrally different light to the eye. We therefore suggest that the organization of human color vision according to four-color classes (reds, greens, blues, and yellows) has arisen as a solution to this logical requirement in topology.

Animals↗

PubMed2000

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Journal Article↗

PubMed1999

An empirical explanation of the cornsweet effect.

A long-standing puzzle in vision is the assignment of illusory brightness values to visual territories based on the characteristics of their edges (the Craik-O'Brien-Cornsweet effect). Here we show that the perception of the equiluminant territories flanking the Cornsweet edge varies according to whether these regions are more likely to be similarly illuminated surfaces having the same material properties or unequally illuminated surfaces with different properties. Thus, if the likelihood is increased that these territories are surfaces with similar reflectance properties under the same illuminant, the Craik-O'Brien-Cornsweet effect is diminished; conversely, if the likelihood is increased that the adjoining territories are differently reflective surfaces receiving different amounts of illumination, the effect is enhanced. These findings indicate that the Craik-O'Brien-Cornsweet effect is determined by the relative probabilities of the possible sources of the luminance profiles in the stimulus.

Computer Graphics↗

PubMed1999

An empirical basis for Mach bands.

Mach bands, the illusory brightness maxima and minima perceived at the initiation and termination of luminance gradients, respectively, are generally considered a direct perceptual manifestation of lateral inhibitory interactions among retinal or other lower order visual neurons. Here we examine an alternative explanation, namely that Mach bands arise as a consequence of real-world luminance gradients. In this first of two companion papers, we analyze the natural sources of luminance gradients, demonstrating that real-world gradients arising from curved surfaces are ordinarily adorned by photometric highlights and lowlights in the position of the illusory bands. The prevalence of such gradients provides an empirical basis for the generation of this perceptual phenomenon.

Animals↗

PubMed1999

Mach bands as empirically derived associations.

If Mach bands arise as an empirical consequence of real-world luminance profiles, several predictions follow. First, the appearance of Mach bands should accord with the appearance of naturally occurring highlights and lowlights. Second, altering the slope of an ambiguous luminance gradient so that it corresponds more closely to gradients that are typically adorned with luminance maxima and minima in the position of Mach bands should enhance the illusion. Third, altering a luminance gradient so that it corresponds more closely to gradients that normally lack luminance maxima and minima in the position of Mach bands should diminish the salience of the illusion. Fourth, the perception of Mach bands elicited by the same luminance gradient should be changed by contextual cues that indicate whether the gradient is more or less likely to signify a curved or a flat surface. Because each of these predictions is met, we conclude that Mach bands arise because the association elicited by the stimulus (the percept) incorporates these features as a result of past experience.

Computer Simulation↗

PubMed1999

The effects of color on brightness.

Observation of human subjects shows that the spectral returns of equiluminant colored surrounds govern the apparent brightness of achromatic test targets. The influence of color on brightness provides further evidence that perceptions of luminance are generated according to the empirical frequency of the possible sources of visual stimuli, and suggests a novel way of understanding color contrast and constancy.

Color Perception↗

PubMed1999

Interindividual variation in human visual performance.

The responses of 20 young adult emmetropes with normal color vision were measured on a battery of visual performance tasks. Using previously documented tests of known reliability, we evaluated orientation discrimination, contrast sensitivity, wavelength sensitivity, vernier acuity, direction-of-motion detection, velocity discrimination, and complex form identification. Performance varied markedly between individuals, both on a given test and when the scores from all tests were combined to give an overall indication of visual performance. Moreover, individual performances on tests of contrast sensitivity, orientation discrimination, wavelength discrimination, and vernier acuity covaried, such that proficiency on one test predicted proficiency on the others. These results indicate a wide range of visual abilities among normal subjects and provide the basis for an overall index of visual proficiency that can be used to determine whether the surprisingly large and coordinated size differences of the components of the human visual system (Andrews, Halpern, & Purves, 1997) are reflected in corresponding variations in visual performance.

Adult↗

PubMed1998

The influence of depicted illumination on brightness.

The striking illusions produced by simultaneous brightness contrast generally are attributed to the center-surround receptive field organization of lower order neurons in the primary visual pathway. Here we show that the apparent brightness of test objects can be either increased or decreased in a predictable manner depending on how light and shadow are portrayed in the scene. This evidence suggests that perceptions of brightness are generated empirically by experience with luminance relationships, an idea whose implications we pursue in the accompanying paper.

Computer Graphics↗

PubMed1998

An empirical explanation of brightness.

In this second part of our study on the mechanism of perceived brightness, we explore the effects of manipulating three-dimensional geometry. The additional scenes portrayed here demonstrate that the same luminance profile can elicit different sensations of brightness as a function of how the objects in the scene are arranged in space. This further evidence confirms the implication of the scenes presented in the accompanying paper, namely that sensations of relative brightness-including standard demonstrations of simultaneous brightness contrast-cannot arise by computations of local contrast. The most plausible explanation of the full range of perceptual phenomena we have described is an empirical strategy that links the luminance profile in a visual stimulus with an association (the percept) that represents the profile's most probable real-world source.

Contrast Sensitivity↗

PubMed1998

The distribution of oriented contours in the real world.

In both humans and experimental animals, the ability to perceive contours that are vertically or horizontally oriented is superior to the perception of oblique angles. There is, however, no consensus about the developmental origins or functional basis of this phenomenon. Here, we report the analysis of a large library of digitized scenes using image processing with orientation-sensitive filters. Our results show a prevalence of vertical and horizontal orientations in indoor, outdoor, and even entirely natural settings. Because visual experience is known to influence the development of visual cortical circuitry, we suggest that this real world anisotropy is related to the enhanced ability of humans and other animals to process contours in the cardinal axes, perhaps by stimulating the development of a greater amount of visual circuitry devoted to processing vertical and horizontal contours.

Animals↗

PubMed1998

Unequal representation of cardinal and oblique contours in ferret visual cortex.

We have measured the amount of cortical space activated by differently oriented gratings in 25 adult ferrets by optical imaging of intrinsic signal. On average, 7% more area of the exposed visual cortex was preferentially activated by vertical and horizontal contours than by contours at oblique angles. This anisotropy may reflect the real-world prevalence of contours in the cardinal axes and could explain the greater sensitivity of many animals to vertical and horizontal stimuli.

Animals↗

PubMed1997

Similarities in normal and binocularly rivalrous viewing.

We report here a series of observations-most of which the reader can experience directly-showing that distinct components of patterned visual stimuli (orthogonal lines of a different hue) vary in perception as sets. Although less frequent and often less complete, these perceptual fluctuations in normal viewing are otherwise similar to the binocular rivalry experienced when incompatible scenes are presented dichoptically.

Humans↗

PubMed1997

The perception of transparent three-dimensional objects.

When the proximal and distal elements of wire-frame cubes are conflated, observers perceive illusory structures that no longer behave veridically. These phenomena suggest that what we normally see depends on visual associations generated by experience. The necessity of such learning may explain why the mammalian visual system is subject to a prolonged period of plasticity in early life, when novel circuits are made in enormous numbers.

Aging↗

PubMed1997

Correlated size variations in human visual cortex, lateral geniculate nucleus, and optic tract.

We have examined several components of the human visual system to determine how the dimensions of the optic tract, lateral geniculate nucleus (LGN), and primary visual cortex (V1) vary within the same brain. Measurements were made of the cross-sectional area of the optic tract, the volumes of the magnocellular and parvocellular layers of the LGN, and the surface area and volume of V1 in one or both cerebral hemispheres of 15 neurologically normal human brains obtained at autopsy. Consistent with previous observations, there was a two- to threefold variation in the size of each of these visual components among the individuals studied. Importantly, this variation was coordinated within the visual system of any one individual. That is, a relatively large V1 was associated with a commensurately large LGN and optic tract, whereas a relatively small V1 was associated with a commensurately smaller LGN and optic tract. This relationship among the components of the human visual system indicates that the development of its different parts is interdependent. Such coordinated variation should generate substantial differences in visual ability among humans.

Adult↗

PubMed1996

The extraordinarily rapid disappearance of entoptic images.

It has been known for more than 40 years that images fade from perception when they are kept at the same position on the retina by abrogating eye movements. Although aspects of this phenomenon were described earlier, the use of close-fitting contact lenses in the 1950s made possible a series of detailed observations on eye movements and visual continuity. In the intervening decades, many investigators have studied the role of image motion on visual perception. Although several controversies remain, it is clear that images deteriorate and in some cases disappear following stabilization; eye movements are, therefore, essential to sustained exoptic vision. The time course of image degradation has generally been reported to be a few seconds to a minute or more, depending upon the conditions. Here we show that images of entoptic vascular shadows can disappear in less than 80 msec. The rapid vanishing of these images implies an active mechanism of image erasure and creation as the basis of normal visual processing.

Arterioles↗