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PubMed1987

Developmental aspects of experimental myopia in chicks: susceptibility, recovery and relation to emmetropization.

Chicks deprived of form-vision in the lateral part of their visual fields become severely myopic largely because of elongation of the vitreous chamber. The myopia mostly affects the visually deprived nasal retina; the nondeprived temporal retina is unaffected. These changes occur most rapidly early in life, being evident then after only 3 days of visual restriction. The susceptibility declines with age, being proportional to the rate of increase of axial length. Recovery from this myopia occurs if the visual restriction is removed during the first 6 weeks of life, as a result of the cessation of elongation of the vitreous chamber. The rate of recovery is directly related to the degree of myopia and inversely related to age. The pattern of changes in refractive status and variability argue for the probable existence of an active mechanism regulating eye growth in a manner dependent on refractive error, thereby producing emmetropization.

Accommodation, Ocular↗
PubMed1987

Dioptric and non-dioptric stimuli for accommodation: target size alone and with blur and chromatic aberration.

The frequency response of the accommodative system (0.05-1 Hz) was determined for various combinations of stimuli: changing target size was presented alone, together with defocus blur, and with both defocus blur and chromatic aberration. A high-speed infrared optometer monitored accommodation while the subject viewed the target in a Badal optometer. Target size was varied sinusoidally and blur was provided by moving the target towards and away from the subject at the same frequency. Chromatic aberration was controlled by using either monochromatic (590 nm) or white (3300 K) light. The target was presented under open-loop conditions when size was the only stimulus. We find that besides the conventional dioptric stimuli, changes in target size that result in changes in apparent distance can have substantial effects on accommodation.

Accommodation, Ocular↗
PubMed1987

The effects of optical vergence, contrast, and luminance on the accommodative response to spatially bandpass filtered targets.

The steady-state monocular accommodative response was measured using a new type of stimulus, a spatially bandpass filtered luminance distribution known as a difference of Gaussian or DOG. The independent variables were: spatial frequency, optical vergence, contrast, and mean luminance. High-contrast DOGs of varying peak spatial frequencies were presented monocularly over a range of target optical vergences. In addition, DOGs were presented at a fixed dioptric vergence (1) over a range of contrasts with a constant mean luminance, and (2) over a range of mean luminances with a constant contrast. The magnitude of the accommodative error was found to depend on the total stimulus condition, i.e. the particular level of each independent variable. Changes in retinal-image contrast from the background (zero-defocus) level, which were brought about by the errors of accommodation under the various stimulus conditions, were mathematically determined and were used to calculate the "accommodative (contrast discrimination) Weber fractions". Comparisons between accommodative and psychophysical contrast discrimination data revealed that there are limits to the degree of shared processing of contrast discrimination information between accommodation and visual perception.

Accommodation, Ocular↗
PubMed1987

Human optokinetic nystagmus in response to moving binocularly disparate stimuli.

Physiological and behavioral evidence shows that the directionally preponderant subcortical control of optokinetic nystagmus (OKN) in lower mammals is supplemented in higher mammals by bidirectional cortical control. It is hypothesized that this cortical control allows higher mammals to cope with the parallactic movement of the scene produced by linear motion of the body. In particular, it is hypothesized that a coupling between OKN and stereopsis allows higher mammals to stabilize the images of objects within the plane of fixation while ignoring motion signals from objects at other distances. According to this hypothesis the gain of the slow phase of OKN should be highest for binocularly fused moving stimuli and attenuated for binocularly disparate displays. The results of Experiment 1 confirmed this prediction although the effects of accommodation were not ruled out completely. In Experiment 2 a display moving in one direction was presented across the central retina at the same time as one moving in the opposite direction was presented in the upper and lower periphery. It was found that subjects do not show OKN in the direction of the peripheral display unless it is binocularly fused and the central display is disparate. In Experiment 3 a stationary display of dots was superimposed on a moving display. It was found that OKN is not inhibited by the stationary display when it has a horizontal disparity and the moving display is fused. Experiment 4 found that horizontal OKN is disrupted by the sudden introduction of a vertical disparity in the stimulus. Since accommodative state was kept constant in the last three experiments, the data show that binocular disparities can help a person to stabilize selectively the image of one moving display while ignoring conflicting motion signals from another display.

Accommodation, Ocular↗
PubMed1987

Accommodation in infants as measured by photorefraction.

We developed a video camera photorefractive procedure that allows on-line monitoring of accommodation from a distance of 1-2m, and have used it to study accommodation in twenty-nine 2- to 10-month-old human infants. We presented square wave gratings and random checkerboard targets at 25, 33, 50, and 100 cm from the infant. All infants altered their accommodation in the appropriate direction for changing target distances. We also presented infants with a slowly rotating circular striped target. We did not observe any systematic change in accommodation of the astigmatic infants to the rotating striped target, nor any significant change in their accommodation to stationary targets as a function of target type. Measured speeds of accommodation in infants were at least 4.6 D/sec, comparable to that found for adults.

Accommodation, Ocular↗
PubMed1987

Compensatory eye movements during active head rotation for near targets: effects of imagination, rapid head oscillation and vergence.

Because the center of natural head rotation lies some distance behind the centers of eye rotation, the VOR has to operate with a gain substantially above 1 for there to be stable fixation of targets lying near the head. In humans, VOR gain was increased inversely proportional to fixation distance and changed with the angle of the head for very near targets. These effects were also evident when the subject imagined the target. However, this "high-gain" VOR was found to deteriorate substantially at frequencies beyond ca 2.5 Hz. In conditions without visual feedback, the VOR gain enhancement due to near fixation was disrupted by monocular viewing. When the subjects wore lenses to relax or increase accommodation, the lenses were found to have no effect on VOR gain. On the other hand, prisms of equivalent power to the lenses had a large effect whereby gain was adjusted according to the vergence state of the eyes. This suggests that VOR gain modulation is under the direct control of convergence.

Accommodation, Ocular↗
PubMed1987

Changes in corneal curvature during accommodation in chicks.

Evidence is presented for an active corneal component of accommodation in chicks. Using anesthetized chicks, consistent increases in corneal curvature were observed during accommodation produced either by electrical stimulation of the Edinger-Westphal nucleus or by topical application of 0.4% nicotine sulfate to the cornea. Electrical stimulation produced a mean accommodative amplitude of 9.2 diopters (D) and a change in corneal power of 3.9 D whereas nicotine treatment elicited 15.1 D of accommodation and 6.1 D of change in corneal power. The change in corneal power increased proportionately with accommodative amplitude up to about 10 D of total accommodation where the corneal power change appeared to level off at approximately 6 D. This limit to corneal curvature change implies that it plays a proportionately greater role in the lower range of accommodation.

Accommodation, Ocular↗
PubMed1987

Aging and human macular pigment density. Appended with translations from the work of Max Schultze and Ewald Hering.

The optical density of human macular pigment was measured for 50 observers ranging in age from 10 to 90 years. The psychophysical method required adjusting the radiance of a 1 degree, monochromatic light (400-550 nm) to minimize flicker (15 Hz) when presented in counterphase with a 460 nm standard. This test stimulus was presented superimposed on a broad-band, short-wave background. Macular pigment density was determined by comparing sensitivity under these conditions for the fovea, where macular pigment is maximal, and 5 degrees temporally. This difference spectrum, measured for 12 observers, matched Wyszecki and Stiles's standard density spectrum for macular pigment. To study variation in macular pigment density for a larger group of observers, measurements were made at only selected spectral points (460, 500 and 550 nm). The mean optical density at 460 nm for the complete sample of 50 subjects was 0.39. Substantial individual differences in density were found (ca. 0.10-0.80), but this variation was not systematically related to age.

Accommodation, Ocular↗
PubMed1988

Visual sensitivity to temporal change in focus and its relevance to the accommodation response.

Measurements were made of the ability of observers, whose accommodation had been paralysed, to detect the small changes in contrast resulting from sinusoidal, oscillatory changes in the dioptric focus of test objects, as a function of the mean position of focus. Variables studied included the form and wavelength composition of the test object, the diameter of the entrance pupil of the eye and the temporal frequency of the focus change. The dioptric amplitudes of the thresholds found (approximately 0.1 D) were comparable with the normally observed amplitudes of the microfluctuations of the accommodation system of the eye. A maximum for the threshold change of focus was found to occur about a mean position of focus corresponding to the nominal "best-focus". Two threshold minima occurred symmetrically on either side of this position of optimal mean focus; the positions of these minima depended on the spatial frequency content of the test object and the pupil diameter. The results are interpreted in terms of the corresponding through-focus changes in optical modulation transfer of the eye and data on the sensitivity of the visual system to spatial and temporal modulation. For sinusoidal grating test objects, it appears that the results can qualitatively be explained if it is assumed that the detectable focus change is such that the ratio of the modulation change in the retinal image, produced by the focus change, to the modulation at the mean position of focus is constant. Results for targets of broad spatial bandwidth suggest that sensitivity to focus change may be dominated by spatial frequency components approximately 5 c/deg. The implications of the data for the understanding of the accommodation control system are briefly considered.

Accommodation, Ocular↗
PubMed1988

A hand optometer for measuring dark focus.

To measure the accommodative state of the eye in a stimulus free condition, the so called dark focus, a simple optometer was constructed based on the principle of the polarized vernier optometer originally proposed by Moses (1971). Data obtained with this hand optometer were compared with those of two other subjective techniques, the polarized vernier optometer and the laser optometer, we were found to be similar. The advantage of this hand optometer is that it is a convenient device that allows one to measure the dark focus within minutes, under normal room lighting.

Accommodation, Ocular↗
PubMed1988

Changing size (looming) as a stimulus to accommodation and vergence.

Changing size (looming) produces changes in accommodation and vergence. Dynamic responses of vergence and accommodation to sinusoidal looming of a Maltese cross were recorded with an SRI dual-Purkinje-image eyetracker and optometer. The ratio of these two motor responses was compared with the response accommodative convergence/accommodation (AC/A) ratio and convergence accommodation/convergence (CA/A) ratio determined from sinusoidal variations of blur and disparity respectively. The response to changing size was found to be more similar to the AC/A ratio than the CA/C ratio. In addition, when a changing disparity or changing blur stimulus was combined with a changing size stimulus, the response phase lags of accommodation and vergence were decreased. In addition, the CA/C ratio was increased when changing size was added to changing disparity, but the AC/A ratio was unaltered when changing size was added to changing blur. These results indicate that changing size is stimulating accommodation directly and vergence secondarily through an AC/A crosslink.

Accommodation, Ocular↗
PubMed1988

Accommodation, refractive error and eye growth in chickens.

We raised chickens with defocusing lenses of differing powers in front of their eyes. For this purpose, small hoods made from soft, thin leather were carefully fitted to their heads. Lenses were attached to the hoods by velcro fasteners and could be easily removed for cleaning. The powers of the lenses were such that their optical effects could be compensated for by accommodation. It was verified by infrared (IR) photoretinoscopy that the chickens could keep their retinal images in focus. Wearing a lens resulted in a consistent shift of the non cycloplegic refractive state (measured without the lens) which was in the direction to compensate for the lens. We used a sensitive technique (precision = +/- 50 micron as estimated from the variability of repeated measurements) to measure the posterior nodal distance (PND) in excised eyes of birds grown with lenses. The PND, in turn, was used to compare eyes treated with different lenses. It was found that the PND was increased in eyes which were treated with negative lenses compared to those treated with positive lenses. This effect occurs independently in both eyes and it is not due to changes in corneal curvature. We discuss our result in terms of a closed-loop feedback system for the regulation of eye growth.

Accommodation, Ocular↗
PubMed1988

Do target angular size-change and blur cues interact linearly in the control of human accommodation?

Calculations made using the data of Kruger and Polar [J. opt. Soc. Am. A2, 1832-1835 (1985); Vision Res. 26, 957-971 (1986); Vision Res. 27, 555-567 (1987)] show that for three of the four subjects they studied, size-change and blur cues do not interact linearly in the control of accommodation. A simple non-linear interaction model is shown to fit the data for all four subjects.

Accommodation, Ocular↗
PubMed1988

Effects of temporal frequency on the contrast sensitivity of the human accommodation system.

Contrast thresholds were determined for the initiation of accommodative responses to drifting sine-wave stimuli (4.1 c/deg) over a range of temporal frequencies (0-14.0 Hz). Accommodation was monitored with a dynamic infrared optometer. Psychophysical detection thresholds were also determined for the same stimuli. A comparison of the contrast thresholds for detection with those for the initiation of accommodation indicates that these two tasks are mediated by mechanisms of comparable sensitivity. Examination of the effects of temporal frequency on the contrast sensitivity of these two visual tasks reveals modest differences in the tuning properties of the underlying sensory mechanisms. Transient mechanisms tuned to intermediate temporal frequencies appear to have a greater role in the initiation of accommodative responses to grating stimuli than in the detection of such stimuli.

Accommodation, Ocular↗
PubMed1989

Computing high order wave aberration coefficients from variations of best focus for small artificial pupils.

Van den Brink (1962) measured the variation of best focus of vertical bar targets through a 1.4 mm aperture across the pupil of the eye. He expressed his results in contour maps of isodioptric lines across the pupil. The relative focus of a portion of the pupil is a function of the curvature of the wave front within the aperture. The curvature, in turn, is proportional to the second derivative of the wave aberration polynomial. Thus it is possible to make estimates of some of the coefficients of the wave aberration polynomial from Van den Brink's focusing data. This has been done for two states of accommodation. The results indicate that the wave aberration polynomial of the measured eye contains some significant terms of a power higher than hitherto measured.

Accommodation, Ocular↗
PubMed1989

Acuity for fine-grain motion and for two-dot spacing as a function of retinal eccentricity: differences in specialization of the central and peripheral retina.

The brief presentation in the peripheral field of two closely spaced luminous point stimuli, in rapid sequence, induces the illusion of a single dot moving over an extended path. This fine-grain movement illusion (FGMI) is particularly compelling under conditions of dark adaptation. The strength of the motion percept, assessed by a rating-scale procedure, was found to correlate well, over different flash-flash onset delays, with an objective measure of the illusion requiring discrimination of the direction of the flash-flash sequence. A direction-discrimination measure was used to determine the minimum dot separation that would reliably elicit an FGMI at retinal eccentricities of 5-25 deg. For comparison, measures of static spatial acuity was made based on the minimum angle of resolution of two simultaneous dot flashes, and on the threshold for discriminating the separation of two simultaneous dot flashes with variable initial spacing. The spatial threshold for FGMI was lower than that for each of the static measures at all peripheral eccentricities, and it increased more slowly with eccentricity than the other spatial thresholds, suggesting the involvement of separate visual pathways for generating percepts of motion and percepts of shape or location. The finding that in the periphery the grain for motion detection was finer than that for spatial discrimination constrains a class of motion-perception models that form an initial spatial description of the stimulus and then compute a temporal derivative.

Accommodation, Ocular↗
PubMed1990

Readily visible changes in color contrast are insufficient to stimulate accommodation.

In an earlier study (Wolfe & Owens, 1981) it was reported that humans could not accommodate to an insoluminant red-green border. However, recent masking studies (Switkes, Bradley & DeValois, 1988) have shown that, using an appropriately normalized contrast metric, contrast decrements similar to those produced by defocus are equally visible for color or luminance modulated grating patterns. We have compared accommodative responses to 1.75 c/deg gratings that consisted of either isochromatic luminance modulations or isoluminant red-green color modulations. All four observers could accommodate accurately to luminance modulated gratings over a wide range of contrasts. However, no appropriate accommodative responses were obtained even for the highest contrast color modulated gratings. These results show the changes in color contrast are ineffective as stimuli for the human accommodative response even when the changes in chromatic contrast accompanying defocus are readily perceived.

Accommodation, Ocular↗
PubMed1990

The optical transverse chromatic aberration on the fovea of the human eye.

The horizontal component of optical transverse chromatic aberration (TCA) at the fovea between 486 and 656 nm is measured in a sample of 8 eyes by two novel methods, both using vernier adjustment tasks with a retinal illumination of approx. 780 td and for a pupil size of approximately 5.5 mm dia. Initially, in an indirect method, TCA is derived along the line of sight from chromatic parallax. Secondly, TCA is measured directly using a semi-Maxwellian view and compensating for longitudinal chromatic aberration (LCA). Both techniques are unaffected by coma or by the Stiles-Crawford effects, thus optical TCA rather than the TCA perceived in normal view is measured. On average, optical TCA is in the same direction but less than previously predicted by eye models and predictions of the optical quality of the eye in white light are modified. Factors underlying the lower average value of optical TCA and variability among subjects, especially pupil centration and foveal position, are discussed. The relationship of optical TCA to TCA perceived in normal view and to chromostereopsis is analysed. The results suggest that the optical design of the human eye is optimized to reduce the wavelength dependent phase shift in the optical transfer function, which could be produced by optical TCA.

Accommodation, Ocular↗