Structurally and functionally, the short-wave-sensitive (S) cone pathways are thought to decline more rapidly with normal aging than the middle- and long-wave-sensitive cone pathways. This would explain the celebrated results by Verriest and others demonstrating that the largest age-related color discrimination losses occur for stimuli on a tritan axis. Here, we challenge convention, arguing from psychophysical data that selective S-cone pathway losses do not cause declines in color discrimination. We show substantial declines in chromatic detection and discrimination, as well as in temporal and spatial vision tasks, that are mediated by S-cone pathways. These functional losses are not, however, unique to S-cone pathways. Finally, despite reduced photon capture by S cones, their postreceptoral pathways provide robust signals for the visual system to renormalize itself to maintain nearly stable color perception across the life span.

An impulse response function (IRF) to a luminous pulse was derived for 70 normal observers ranging in age from 16 to 86 years. Thresholds were measured for two pulses separated by interstimulus intervals from 6.7 to 180 ms. The pulses had a spatial Gaussian shape (+/-1SD=2.3 degrees diam) and were presented as increments on a 10 cd/m(2) background, having the same chromaticity as the pulse. A spatial 4-alternative forced-choice method was combined with a staircase procedure. Retinal illuminance was equated individually by heterochromatic flicker photometry and control of pupil area. Each IRF was measured four times, in separate sessions, for each observer. IRFs calculated from the threshold data revealed significant age-related changes in the response amplitude of both excitatory and inhibitory phases. In general, there were no significant changes in the time to the first peak or in the first zero crossing. For 12 of 20 observers over 60 years of age, however, the amplitude of the second (inhibitory) phase was reduced relative to the excitatory phase so their IRFs were quite slow and long. Control conditions with three pseudophakic observers and two normal observers with induced blur demonstrated that age-related changes in the IRF under these conditions cannot be ascribed to optical factors. The data suggest that the human visual system generally maintains a stable speed of response to a flash until at least about 80 years of age, even while there are senescent reductions in response signal amplitude.

The chromatic content (saturation) of monochromatic stimuli (480, 505, 577, and 650 nm) was scaled as a function of field size at three different retinal locations by 58 observers ranging from 18 to 83 yr of age. The different retinal locations (6 deg nasal, 2.5 deg inferior and 6 deg temporal eccentricity) were chosen according to anatomical studies demonstrating different degrees of senescent losses of cones or ganglion cells. Nine field sizes were tested, ranging from 0.0096 to 0.96 deg in diameter. The subjects used a percentage scale to judge the saturation of the flashed stimulus presentations (2 s on, 5 s off). The data analysis demonstrated that older observers require larger field sizes than younger observers to perceive hue as well as larger field sizes to reach the same level of scaled saturation. The spatial dependency of color appearance for younger and older observers was not correlated with senescent losses in retinal cells reported for the different retinal locations. The data were modeled by using an impulse-response function (i.e., Naka-Rushton equation) so that perceptive fields could be compared to electrophysiological measures of receptive fields or dendritic fields of retinal and cortical cells.

The retinal image is sampled concurrently, and largely independently, by three physiologically and anatomically distinct pathways, each with separate ON and OFF subdivisions. The retinal circuitry giving rise to an ON pathway receiving input from the short-wave-sensitive (S) cones is well understood, but the S-cone OFF circuitry is more controversial. Here, we characterize the temporal properties of putative S-cone ON and OFF pathways in younger and older observers by measuring thresholds for stimuli that produce increases or decreases in S-cone stimulation, while the middle- and long-wave-sensitive cones are unmodulated. We characterize the data in terms of an impulse response function, the theoretical response to a flash of infinitely short duration, from which the response to any temporally varying stimulus may be predicted. Results show that the S-cone response to increments is faster than to decrements, but this difference is significantly greater for older individuals. The impulse response function amplitudes for increment and decrement responses are highly correlated across individuals, whereas the timing is not. This strongly suggests that the amplitude is controlled by neural circuitry that is common to S-cone ON and OFF responses (photoreceptors), whereas the timing is controlled by separate postreceptoral pathways. The slower response of the putative OFF pathway is ascribed to different retinal circuitry, possibly attributable to a sign-inverting amacrine cell not present in the ON pathway. It is significant that this pathway is affected selectively in the elderly by becoming slower, whereas the temporal properties of the S-cone ON response are stable across the life span of an individual.

Age-related changes in the temporal properties of an S-cone pathway were characterized by the psychophysical impulse-response function (IRF). Participants included 49 color-normal observers ranging in age from 16.8 to 86.3 years. A double-pulse method was used to measure the IRF with S-cone modulation at constant luminance. Stimuli were presented as a Gaussian patch (+/-1SD = 2.3 degrees ) in one of four quadrants around a central fixation cross on a CRT screen. The test stimulus was modulated from the equal-energy white of the background toward the short-wave spectrum locus. Each of the two pulses (6.67 ms) was separated by an interstimulus interval (ISI) from 20 to 720 ms. Chromatic detection thresholds were determined by a four-alternative forced-choice method with staircases for each ISI in one session. IRFs were calculated from the threshold data using a model with four parameters of an exponentially damped sine wave. S-cone IRFs have only an excitatory phase and a much longer time course compared with IRFs for luminance modulation measured with the same apparatus. The results demonstrated significant age-related losses in IRF amplitude, but the latency (time to peak) of the IRF was stable with age.

© OSA 2014. We illustrate a high-speed (100 kHz) high penetration phase stabilized swept source optical coherence angiography (SSOCA) system for in vivo volumetric depth-resolved vasculature imaging of anterior and posterior segment of human eye.

Color induction was measured using a matching method for two spatial patterns, each composed of double contours. In one pattern (the standard), the contours had sharp edges to induce the Watercolor Effect (WCE); in the other, the two contours had a spatial taper so that the overall profile produced a sawtooth edge, or ramped stimulus. These patterns were chosen based on our previous study demonstrating that the strength of the chromatic WCE depends on a luminance difference between the two contours. Low-pass chromatic mechanisms, unlike bandpass luminance mechanisms, may be expected to be insensitive to the difference between the two spatial profiles. The strength of the watercolor spreading was similar for the two patterns at narrow widths of the contour possibly because of chromatic aberration, but with wider contours, the standard stimulus produced stronger assimilation than the ramped stimulus. This research suggests that luminance-dependent chromatic mechanisms mediate the WCE and that these mechanisms are sensitive to differences in the two spatial profiles of the pattern contours only when they are wide.

A new visual phenomenon that we call flashing anomalous color contrast is described. This phenomenon arises from the interaction between a gray central disk and a chromatic annulus surrounded by black radial lines. In an array of such figures, the central gray disk no longer appears gray, but assumes a color complementary to that of the surrounding annulus. The induced color appears: (1) vivid and saturated; (2) self-luminous, not a surface property; (3) flashing with eye or stimulus movement; (4) floating out of its confines; and (5) stronger in extrafoveal than in foveal vision. The strength of the effect depends on the number, length, width, and luminance contrast of the radial lines. The results suggest that the chromatic ring bounding the inner tips of the black radial lines induces simultaneous color contrast, whereas the radial lines elicit, in conjunction with the gray disk and the ring, the flashing, vividness, and high saturation of the effect. The stimulus properties inducing the illusion suggest that flashing anomalous color contrast may be based on asynchronous interactions among multiple visual pathways.

The watercolor effect is perceived when a dark (e.g., purple) contour is flanked by a lighter chromatic contour (e.g., orange). Under these conditions, the lighter color will assimilate over the entire enclosed area. This filling-in determines figure-ground organization when it is pitted against the classical Gestalt factors of proximity, good continuation, closure, symmetry, convexity, as well as amodal completion, and past experience. When it is combined with a given Gestalt factor, the resulting effect on figure-ground organization is stronger than for each factor alone. When the watercolor effect is induced by a dark red edge instead of an orange edge, its figural strength is reduced, but still stronger than without it. Finally, when a uniform surface is filled physically using the color of the orange fringe, figure-ground organization is not different from that for the purple contour only. These findings show that the watercolor effect induced by the edge could be an independent factor, different from the classical Gestalt factors of figure-ground organization.

Neural contributions to the age-related reduction in spatial vision are incontrovertible. Whether there are differential age-related changes in the magnocellular (M) and parvocellular (P) pathways across the life span has not been tested extensively. We studied psychophysically the contrast gain signature of the M and P pathways for 13 younger and 13 older observers. Two separate paradigms thought to separate the M and P pathways based on their contrast gain (J. Pokorny & V. C. Smith, 1997) signature were used. A four-square array was presented as an increment or decrement on a background of 115 Td for 35 ms, with one test square presented at a slightly higher or lower retinal illumination. Using a four-alternative forced-choice procedure, the observer's task was to choose the unique square. The two paradigms differed only in the pretrial adaptation and inter-stimulus array. Data were fitted with models of contrast discrimination derived from the unique contrast gain signatures. The fitted models indicate a change in the discrimination functions with age for both the M and P pathways, revealing a shift in the contrast gain slope. Results indicate that both M and P pathways undergo age-related changes, but functional losses appear greater for the P pathway under the conditions tested.