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PubMedDate not supplied

Motion aftereffect transfer in the monofixation syndrome.

If one adapts to a moving repetitive stimulus of stripes that is suddenly stopped, the stripes will appear to move backward. This apparent backward motion is the motion aftereffect (MAE), and its duration is a measure of its magnitude. If one eye adapts to the moving stimulus and the other eye experiences the aftereffect to the stationary stimulus, the aftereffect has been transferred from one eye to the other and is termed the interocular transfer of the MAE. Experimental evidence indicates that the degree of MAE transfer correlates with clinical binocularity. This study compares the MAE transfer in six subjects with the monofixation syndrome to five normal subjects. The stimuli used are sinusoidal stripes generated on two cathode-ray tubes, subtending either 8 degrees or 2 degrees of visual angle with a periodicity of either 0.5 or 3 cycles/degree presented haploscopically. Subjects with the monofixation syndrome differed significantly from normal subjects in the amount of MAE transferred, implying a lack of central neuronal connections in addition to those mediating conscious central fusion in clinical sensory testing.

Adaptation, Physiological↗
PubMed2000

Retinal sensitivity to flicker modulation: reduced by early age-related maculopathy.

PURPOSE: To evaluate retinal, cone-mediated flicker sensitivity (CFS) in age-related maculopathy (ARM) by quantifying response gain and threshold of the focal electroretinogram (FERG) to flicker modulation. METHODS: Nineteen patients with ARM (visual acuity > or =20/30) and 11 age-matched control subjects were examined. Twelve patients had less than 20 soft drusen in the macular region and no hyper-/hypopigmentation (early lesion), whereas seven had more than 20 soft drusen and/or focal hyper-/hypopigmentation (advanced lesion). Macular (18 degree ) FERGs were elicited by a sinusoidally flickering (41 Hz) uniform field (on a light-adapting background) whose modulation depth was varied between 16.5% and 94%. Amplitude and phase of the response's fundamental harmonic were measured. RESULTS: In both control subjects and patients with ARM, log FERG amplitude increased with log stimulus modulation depth with a straight line (power law) relation. However, the slope (or gain) of the function was, on average, steeper in control subjects than in patients with either early or advanced lesions. Mean FERG threshold, estimated from the value of the log modulation depth that yielded a criterion response, did not differ between control subjects and patients with early lesions but was increased (0.35 log units) compared with control subjects in those with advanced lesions. In both patient groups, but not in control subjects, mean FERG phase tended to delay with decreasing stimulus modulation depth. CONCLUSIONS: Retinal CFS losses can be detected in ARM by evaluating the FERG as a function of flicker modulation depth. Reduced response gain and phase delays, with normal thresholds, are associated with early lesions. Increased response thresholds, in addition to gain and phase abnormalities, may reflect more advanced lesions. Evaluating CFS by FERG may directly document different stages of macular dysfunction in ARM.

Aged↗
PubMed1979

Changes in the position of the binoculus with unequal retinal illuminance.

An investigation was carried out into the effect of a monocular neutral density filter on the position of the binoculus. Two experiments were used, and it is postulated that the difference in the results obtained is due to the presence of a motor component in one of the experiments.

Adaptation, Ocular↗
PubMed1980

Adaptation of the binocular rivalry mechanism.

The completeness of binocular rivalry suppression was measured by recording the fraction of a trial during which targets were perceived as alternating in their entirety, rather than blending together into a composite. It was found that the completeness of rivalry declines with prolonged stimulation. A control condition in which subjects saw the same grating targets, but without rivalry, resulted in no decrement. The phenomenon was spatial-frequency specific. The results suggest that binocular rivalry suppression is mediated by a cooperative mechanism which is susceptible to adaptation.

Adaptation, Physiological↗
PubMed2000

Risky driving behavior: a consequence of motion adaptation for visually guided motor action.

The authors examined the effect of adaptation to expansion on overtaking maneuvers in a driving simulator. Following driving on a straight empty road for 5 min, drivers initiated overtaking substantially later (220-510 ms) than comparable maneuvers made following viewing a static scene or following 5 min of curve driving. Following adaptation to contraction (produced by driving backward), observers initiated overtaking significantly sooner. The removal of the road texture significantly reduced the size of the adaptation effect. The authors propose that these changes in overtaking behavior are due to misestimation of the time headway produced by local adaptation of looming detectors that signal motion-in-depth for objects near the focus of expansion. This adaptation effect may increase the risk of rear-end collisions during highway driving.

Adaptation, Psychological↗
PubMed2005

Depth aftereffects mediated by vertical disparities: evidence for vertical disparity driven calibration of extraretinal signals during stereopsis.

Perceptual adaptation often results in a repulsive aftereffect: stimuli are seen as biased away from the adaptation stimulus (). Here we report the absence of a repulsive aftereffect for a vertical gradient of vertical disparity (or vertical size ratio, VSR). We exposed observers to a binocular stimulus consisting of horizontal lines. This stimulus contains vertical, but not horizontal disparities. The visual system was able to measure the VSR of this stimulus: although the lines themselves always appeared unslanted, the VSR carried by the lines had a dramatic effect on the apparent slant of a horizontal row of dots, as predicted by recent accounts of Ogle's (1938) induced effect (e.g., Backus, Banks, van Ee, & Crowell, 1999). Yet we observed no repulsive aftereffect for the VSR signal: after adaptation to horizontal lines that were vertically larger in one eye, we found an attractive aftereffect, the magnitude of which was largest in stimuli that did not contain a VSR signal. We interpret these results as a case of recalibration: disagreement between extra-retinal eye position signals (EP) and VSR causes a recalibration in the use of EP as used in the stereoscopic perception of slant.

Adaptation, Physiological↗
PubMed2005

Life at depth: Photobacterium profundum genome sequence and expression analysis.

Deep-sea life requires adaptation to high pressure, an extreme yet common condition given that oceans cover 70% of Earth's surface and have an average depth of 3800 meters. Survival at such depths requires specific adaptation but, compared with other extreme conditions, high pressure has received little attention. Recently, Photobacterium profundum strain SS9 has been adopted as a model for piezophily. Here we report its genome sequence (6.4 megabase pairs) and transcriptome analysis. The results provide a first glimpse into the molecular basis for life in the largest portion of the biosphere, revealing high metabolic versatility.

Adaptation, Physiological↗
PubMed2005

Thresholds for perception of ripple depth in the passband of a low-pass filter.

Filters are often used in research related to speech and tone perception. Idealized filters with flat pass-bands, flat stop-bands, and infinitely steep rolloff are impossible to implement, thus practical filters often have a frequency response curve that has a certain degree of ripple, and always have finite rolloff. Despite this, there is a dearth of literature concerning the sensitivity of the ear to such artifacts. In the current study we examined the threshold of sensitivity to ripple depth in the pass-band of a digital low pass finite impulse response (FIR) filter. FIR filters are often used due to their lack of phase distortion, and due to the fact that their ripple depth can be closely controlled. Using an adaptive threshold detection paradigm, we found the threshold of noticeable ripple depth to be 2.7 dB (SD = 1.45) for filtered noise, and 4.89 dB (SD = 2.09) for a filtered chirp signal. This is significantly larger than the difference limen in intensity (DLI) for noise or pure tones. Notably, the threshold for filtered noise is significantly lower and more uniform across subjects, compared to the threshold for a filtered chirp signal. We conclude that these issues must be addressed when the necessity for filtering arises, though they cannot be considered independently of the signals themselves.

Acoustic Stimulation↗
PubMed1996

Cyclopean motion perception produced by oscillations of size, disparity and location.

UNLABELLED: For cyclopean and monocularly-visible targets we measured psychophysical thresholds for perceptions produced by the following three stimuli: oscillations of disparity (DO), oscillations of size (SO) and oscillatory motion within the frontoparallel plane (FPO). RESULTS: thresholds for motion in depth perception produced by DO were similar for cyclopean and non-cyclopean targets over the entire 0.25-8 Hz frequency range investigated. Thresholds for perceiving motion in depth produced by SO were considerably (up to 2.5 times) higher for cyclopean targets than for monocularly-visible targets, as were thresholds for perceiving size oscillations. For both cyclopean and monocularly-visible target the perception of motion in depth could be canceled by pitting DO vs SO. Thresholds for perceiving FPO were similar to DO thresholds for the monocularly-visible target, but for the cyclopean targets FPO thresholds rose more steeply than DO thresholds for oscillation frequencies above 1 Hz. CONCLUSIONS: (1) for our subjects, the effective binocular stimulus for motion in depth perception is a rate of change of disparity; an interocular velocity difference is significant only to the extent that it produces a rate of change of disparity. (2) The sensations of motion in depth produced by DO and SO are qualitatively identical. (3) Neural signals produced by DO and SO converge onto a single neural mechanism that signals motion in depth.

Adaptation, Ocular↗
PubMed2003

Adaptive color vision in Pullosquilla litoralis (Stomatopoda, Lysiosquilloidea) associated with spectral and intensity changes in light environment.

Some stomatopod crustacean species that inhabit a range of habitat depths have color vision systems that adapt to changes in ambient light conditions. To date, this change in retinal function has been demonstrated in species within the superfamily Gonodactyloidea in response to varying the spectral range of light. Intrarhabdomal filters in certain ommatidia within the specialized midband of the eye change spectrally, modifying the sensitivity of underlying photoreceptors to match the spectrum of available light. In the present study, we utilized Pullosquilla litoralis, a member of the superfamily Lysiosquilloidea that also has a wide depth range. Individuals were placed within one of three light treatments: (1) full-spectrum, high-intensity 'white' light, (2) narrow-spectrum 'blue' light and (3) full-spectrum, reduced-intensity 'gray' light. After 3 months, the intrarhabdomal filters in Row 3 ommatidia of the midband in blue- and gray-light-treated animals were short-wavelength shifted by 10-20 nm compared with homologous filters in animals in white-light treatments. These spectral changes increase the relative sensitivity of associated photoreceptors in animals that inhabit environments where light spectral range or intensity is reduced. The adaptable color vision system of stomatopods may allow animals to make the best use of the ambient light occurring at their habitat regardless of depth. The major controlling element of the plasticity in lysiosquilloid stomatopod color vision appears to be light intensity rather than spectral distribution.

Adaptation, Ocular↗
PubMed1998

A rotational stereoscopic 3-dimensional movement aftereffect.

A stereoscopic rotational movement aftereffect (MAE) and a stereoscopic bi-directional MAE were generated by rotation of a cyclopean random dot cylinder in depth and by movement of two cyclopean random dot planes in opposite directions, respectively. Cross-adaptational MAEs were also generated on each other, but not with stimuli lacking any disparity. Cross-adaptation MAEs were generated between stereoscopic and non-stereoscopic random dot stimuli moving in the one X/Y plane. Spontaneous reversals in direction of movement were observed with bistable stimuli lacking disparity. Two models of the middle temporal area were considered which might explain both the stereoscopic MAEs and the spontaneous reversals.

Adaptation, Ocular↗
PubMed2003

Attention affects the stereoscopic depth aftereffect.

'Preattentive' vision is typically considered to include several low-level processes, including the perception of depth from binocular disparity and motion parallax. However, doubt was cast on this model when it was shown that a secondary attentional task can modulate the motion aftereffect (Chaudhuri, 1990 Nature 344 60-62). Here we investigate whether attention can also affect the depth aftereffect (Blakemore and Julesz, 1971 Science 171 286-288). Subjects adapted to stationary or moving random-dot patterns segmented into depth planes while attention was manipulated with a secondary task (character processing at parametrically varied rates). We found that the duration of the depth aftereffect can be affected by attentional manipulations, and both its duration and that of the motion aftereffect varied with the difficulty of the secondary task. The results are discussed in the context of dynamic feedback models of vision, and support the penetrability of low-level sensory processes by attentional mechanisms.

Adaptation, Ocular↗
PubMed1984

Discrimination of dynamic interaural intensity differences.

An experiment was conducted to measure observers' ability to detect time-varying interaural intensity differences (IIDs). In a two-interval forced-choice task, observers discriminated a binaural amplitude modulated (AM) noise in which the modulating sinusoid was interaurally in-phase from the same AM noise in which the modulator was interaurally phase-reversed. The latter stimulus produces a sinusoidally varying IID whose rate and peak IID depend on the frequency (fm) and depth (m) of modulation. The carrier was a narrow-band noise, interaurally uncorrelated, centered at 500, 1000, or 4000 Hz. Presentation level was 75 dB SPL; duration was 1.0 s. For a given fm, m was varied in an adaptive procedure to estimate the depth required for 71% discriminability (mthr). Three of the four observers displayed "low-pass" modulation functions: at 500 Hz, as fm increased from 0-50 Hz, mthr increased from 0.08 (IID = 1.3 dB) to 0.50 (peak IID = 9.5 dB). At 1000 and 4000 Hz observers were more sensitive to IID and the functions (mthr vs fm) were flatter than at 500 Hz. Comparison of these data to previously published data indicates that the binaural system can follow fluctuations in IID more efficiently than it can follow fluctuations in interaural time difference, although there are large individual differences in subjects' capacity to process these two types of binaural cues.

Auditory Threshold↗
PubMed1973

Evidence for the existence of neural mechanisms selectively sensitive to the direction of movement in space.

1. Visual sensitivity to movement in depth was measured as a function of the relative distances through which the left and right retinal images moved. This relative distance (left:right ratio) provides a sensitive cue to the direction along which a target moves in three-dimensional space.2. Gazing at a target which moved along a fixed direction in space produced a gross reduction of visual sensitivity to movements in depth along that direction. For other directions of movement, visual sensitivity was not affected.3. Sensitivity to depth movement rapidly rose almost to the preadaptation level within the first 20-60 sec after removing the adapting target, but recovery was not complete until 100-300 min had elapsed.4. Any adapting target whose left:right ratio fell within a definite range gave similar reductions of visual sensitivity to movements in depth. There were five such ranges.5. The effects of adapting to movement in depth suggest that eight mechanisms underlie depth perception. These mechanisms are ;tuned' to the direction of movement in three-dimensional space. Four mechanisms are wholly concerned with movements along directions very close to the line which cuts midway between the eyes, and do not respond to movements whose direction departs by more than 1.5 degrees from the preferred direction.6. Neural mechanisms ;tuned' to different left:right ratios could provide a physiological basis for sensing the direction in which an object moves in three-dimensional space.

Adaptation, Ocular↗
PubMed2000

Color-specific depth mechanisms revealed by a color-contingent depth aftereffect.

Models of stereoscopic depth perception for both natural and random-dot images have focused mainly on the matching of achromatic features of binocular images. Recently, a growing body of research has investigated whether chromatic features can also contribute to the construction of stereoscopic depth. Here we present experiments yielding color-contingent depth aftereffects comparable in magnitude to those measured after adaptation to achromatic stimuli as evidence of neural mechanisms tuned to both color and depth. Furthermore, we report that the locus of the combined processing of color and depth is likely to lie beyond the site of binocular matching.

Adaptation, Physiological↗
PubMed2002

The conjunction of feature and depth information.

By inducing feature-contingent depth aftereffects, we show that the human visual system combines feature information with depth information. These contingent aftereffects were revealed through the use of a novel selective adaptation paradigm whose stimuli required the combination of feature and depth information in order to segment two interleaved, transparent surfaces. We argue that this combined processing exemplifies the remarkable resourcefulness of a visual system that has adapted to exploit conjunctions of cues that can aid in the segmentation of visual surfaces.

Adaptation, Biological↗