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Joel Pokorny

Publications and source records attributed to Joel Pokorny.

At least 19 recordsLinked to original sources
PubMed2006

Visual stimulus-induced changes in human near-infrared fundus reflectance.

PURPOSE: Imaging studies from anesthetized feline, primate, and human retinas have revealed near-infrared fundus reflectance changes induced by visible light stimulation. In the present study, the spatial and temporal properties of similar changes were characterized in normal, awake humans. METHODS: Five normal human subjects were studied. A modified fundus camera was used to image changes in retinal reflectance of 780-nm near-infrared light imaged onto a 12-bit charge-coupled device (CCD) camera in response to a green (540 nm) visual stimulus. During 60 seconds of recording (frame rate, 3 Hz) 10 cycles were recorded, during each of which 3 seconds of blank and then 3 seconds of either vertical bar or blank stimulus was projected. The change in the average near-infrared reflectance of the stimulated retinal region relative to an equal-sized nonstimulated region (r is the ratio of reflectance between the two retinal areas) was analyzed with a mixed model for repeated measures. RESULTS: The mixed model showed a significant average decrease in r of 0.14% (95% CI, -0.25 to -0.03) over all subjects induced by bar stimulus cycles, with a gradual return to baseline after stimulus offset, compared with only a 0.04% (95% CI, -0.11-+0.20) decrease in r induced by blank, nonstimulated cycles. The mixed model for individuals showed a decreasing linear trend in r over time during bar stimulation, but no decrease for blank cycles in three of five subjects. CONCLUSIONS: There was a localized decrease in reflectance in response to 780-nm near-infrared light in the retinal region exposed to a visual stimulus, which was significant in three of five subjects. It is presumed that the reflectance change represents the functional activity of the retina in response to a visual stimulus.

Adult↗
PubMed2005

Audiophile hardware in vision science; the soundcard as a digital to analog converter.

The design objective was to develop an inexpensive digital to analog (D/A) converter for use in vision science. Soundcards are hardware units that can be integral or can be added to a computer to add sound capability. A soundcard contains D/A converters designed to work in the audio frequency range, typically 20-20,000 Hz. Soundcard outputs are high-pass filtered and thus do not convey sub-audio frequency or dc information. It is possible to circumvent this design feature by programming the desired output waveform as an amplitude modulation of a high frequency carrier, and then demodulating the soundcard output. The circuit, using a 20 kHz carrier, provides precise D/A conversion for the frequency range relevant for vision experiments, dc to 100 Hz, using inexpensive readily available components. The specific application was for 8 channels of D/A conversion using a Macintosh computer running under OS X. The software needed to program stimuli was created using CoreAudio, a library for programming sounds in OS X. Using soundcards on other platforms would not be a problem, as long as there exists a low level library that would enable the wave table to be filled.

Brain↗
PubMed2005

Melanopsin-expressing ganglion cells in primate retina signal colour and irradiance and project to the LGN.

Human vision starts with the activation of rod photoreceptors in dim light and short (S)-, medium (M)-, and long (L)- wavelength-sensitive cone photoreceptors in daylight. Recently a parallel, non-rod, non-cone photoreceptive pathway, arising from a population of retinal ganglion cells, was discovered in nocturnal rodents. These ganglion cells express the putative photopigment melanopsin and by signalling gross changes in light intensity serve the subconscious, 'non-image-forming' functions of circadian photoentrainment and pupil constriction. Here we show an anatomically distinct population of 'giant', melanopsin-expressing ganglion cells in the primate retina that, in addition to being intrinsically photosensitive, are strongly activated by rods and cones, and display a rare, S-Off, (L + M)-On type of colour-opponent receptive field. The intrinsic, rod and (L + M) cone-derived light responses combine in these giant cells to signal irradiance over the full dynamic range of human vision. In accordance with cone-based colour opponency, the giant cells project to the lateral geniculate nucleus, the thalamic relay to primary visual cortex. Thus, in the diurnal trichromatic primate, 'non-image-forming' and conventional 'image-forming' retinal pathways are merged, and the melanopsin-based signal might contribute to conscious visual perception.

Animals↗
PubMed2005

Associating color appearance with the cone chromaticity space.

A cone chromaticity space, a transform of a colorimetric specification system into coordinates that represent cone excitations, does not provide color appearance information. Boynton and Olson (Color Research and Application 12, 94-105, 1987) gathered color naming for the 424 Optical Society of America Uniform Color Scales (OSA-UCS) color samples. Here, a computational algorithm was developed that converts OSA-UCS sample values into L, M, S cone excitations based on the 1964 CIE 10 degrees Standard Observer. This makes it possible to plot the cone chromaticities associated with the eight color names used by Boynton and Olsen's observers to describe the non-dark appearing colors.

Algorithms↗
PubMed2005

Matching rod percepts with cone stimuli.

Traditional methods for studying the effects of rod activity on color vision make it hard to assess the underlying physiological mechanisms. In this study, rod-mediated changes in color appearance were assessed by matching them with cone-mediated color changes. A four-primary photostimulator allowed independent control of rod and cone stimulation and identification of the cone types that generate color sensations equivalent to rod color sensations. The results showed that increases in rod stimulation required matches with cone stimuli that excited M-cones more than L-cones for all conditions. Matches for low-luminance conditions also required some S-cone stimulation. A subsidiary experiment showed that increases in rod modulation of an inducing field produced chromatic contrast effects like those produced by the M-cone system. The data are consistent with a hypothesis of perceptual normalization of scotopic vision to the chromatic appearance of objects under photopic conditions.

Color Perception↗
PubMed2004

Contrast-processing deficits in melanoma-associated retinopathy.

PURPOSE: To evaluate the hypothesis that patients with melanoma-associated retinopathy (MAR) have a selective functional loss within the magnocellular (MC) pathway of the cone system, with sparing of parvocellular (PC) pathway function. METHODS: Two patients with MAR, ages 57 and 61 years, with normal Snellen visual acuity, participated in the study. Contrast sensitivity was measured at spatial frequencies ranging from 0.25 to 8 cycles per degree (cpd), using two paradigms (steady pedestal and pulsed pedestal) designed to assess the functional integrity of the MC and PC pathways, respectively. Results in patients with MAR were compared with those in 10 visually normal observers, aged 23 to 57 years. RESULTS: Both patients with MAR showed a loss of contrast sensitivity compared to normal observers, but the pattern of loss differed for the two testing paradigms. For the steady-pedestal paradigm (presumed MC-pathway mediation), the patients' sensitivity loss was greatest at the lowest spatial frequency (0.25 cpd) and the sensitivity loss decreased systematically with increasing spatial frequency. For the pulsed-pedestal paradigm (presumed PC-pathway mediation), the sensitivity loss was greatest at an intermediate spatial frequency of 1 cpd. For both paradigms, the patients' sensitivities were within the normal range at the highest spatial frequency (8 cpd), consistent with their normal visual acuity. CONCLUSIONS: The contrast sensitivity deficits of patients with MAR under photopic conditions are not specific to the MC pathway, as proposed previously, but instead are related to the spatial frequency of the test target. The overall pattern of contrast sensitivity loss shown by the patients with MAR is consistent with the dysfunction at the level of the retinal bipolar cells that is presumed to underlie the MAR syndrome.

Adult↗
PubMed2004

Contrast sensitivity deficits in inferred magnocellular and parvocellular pathways in retinitis pigmentosa.

PURPOSE: To define the contrast sensitivity deficits of patients with retinitis pigmentosa (RP) under testing conditions designed to emphasize threshold mediation by either the magnocellular (MC) or parvocellular (PC) pathway. METHOD: Contrast sensitivity was measured with spatially localized, narrow-band test patterns at peak spatial frequencies ranging from 0.25 to 8 cycles per degree (cpd), using a steady-pedestal paradigm (brief presentation of the test stimulus against a continuously presented luminance pedestal) and a pulsed-pedestal paradigm (simultaneous brief presentation of the test stimulus and luminance pedestal) to favor the MC and PC pathways, respectively. The contrast sensitivity functions of 12 patients with RP who had visual acuities ranging between 20/12.5 and 20/40 were compared to those of 10 visually normal, age-equivalent control observers. RESULTS: Five of the patients with RP who had Snellen visual acuities better than 20/25 had contrast sensitivity functions that were within the normal limits at all spatial frequencies for both testing paradigms. The other seven patients with RP had reduced contrast sensitivities for both paradigms, with the greatest reduction in sensitivity occurring at the highest spatial frequency. Their contrast sensitivity deficits were equivalent for the steady- and pulsed-pedestal paradigms. CONCLUSIONS: As observed in previous studies, the degree of contrast sensitivity loss shown by the patients with RP was greatest at the highest stimulus spatial frequency. However, in comparison to prior studies of contrast discrimination in patients with RP, there was no evidence of a preferential contrast sensitivity loss within the MC pathway. This apparent discrepancy is attributed to differences in the test targets and psychophysical judgments that were used in the studies, which emphasizes the importance of task characteristics in evaluating relative deficits within the MC and PC processing streams in visual disorders.

Adult↗
PubMed2003

Discrimination and identification of luminance contrast stimuli.

The goal of this study was to compare luminance contrast discrimination and polarity identification in the inferred Parvocellular (PC-) and Magnocellular (MC-) pathways. The position identification task tested ability to locate a contrast change within a stimulus. The polarity identification task tested ability to classify the contrast change as either brighter or darker. Three paradigms were employed to find these thresholds for the inferred MC- and PC-pathways: Pulsed-Pedestal, Steady-Pedestal and Pedestal-Delta-Pedestal. Position and polarity identification thresholds were the same for the Pulsed-Pedestal stimuli (inferred PC-pathway). The position identification thresholds were lower than the polarity identification thresholds for Steady-Pedestal stimuli (inferred MC-pathway). The position identification thresholds were lower than the polarity identification thresholds for Pedestal-Delta-Pedestal stimuli when the Delta-Pedestal contrast steps were sub-threshold or close to threshold. When the contrast steps were larger, position identification and polarity identification thresholds were similar for the Pedestal-Delta-Pedestal stimuli. Comparisons were also made between position identification and polarity identification thresholds for a short and a long stimulus presentation. There were no systematic differences dependent on presentation duration.

Adult↗
PubMed2003

Dynamics of sensitivity regulation in primate outer retina: the horizontal cell network.

The goal of these experiments was to define the time course and degree of cone adaptation in primate outer retina by use of probe stimuli upon temporally modulated backgrounds. Recordings were obtained from primate horizontal cells. Test probes were either a low-amplitude, high-frequency sinusoid superimposed on a slowly modulated background or small test pulses superimposed on backgrounds of various frequencies. The amplitude of the test response was modulated by the background, indicating sensitivity regulation. Results were consistent with gain controls which, at 1000 td, required approximately 10-20 ms to completion. These mechanisms could also account for some of the distortions of horizontal cell responses to sinusoids and pulses. Modulation of test responsivity occurred at low background contrasts, suggesting no threshold change in light level must be exceeded to evoke sensitivity regulation. As retinal illuminance increased from darkness, sensitivity regulation was evident at 10-20 td.

Adaptation, Ocular↗
PubMed2003

Spatial frequency processing in inferred PC- and MC-pathways.

The goal of this study was to investigate the role of inferred parvocellular (PC) and magnocellular (MC) pathways in spatial contrast sensitivity. Localized, spatially narrow-band patterns (sixth derivatives of Gaussians, D6s) were presented at various peak spatial frequencies. When the D6 appeared on a pulsed luminance pedestal (Pulsed-Pedestal Paradigm), the spatial contrast sensitivity showed a band-pass shape with good contrast sensitivity at medium spatial frequencies. When the D6 appeared on a steady luminance pedestal (Steady-Pedestal Paradigm), the spatial contrast sensitivity showed a low-pass shape with decreased sensitivity at high spatial frequencies. The band-pass CSF was interpreted as reflecting PC-pathway mediation; the lower spatial frequency region of the low-pass CSF as reflecting MC-pathway mediation.

Contrast Sensitivity↗
PubMed2003

Temporal dynamics of early light adaptation.

This study investigated two aspects of visual sensitivity to a change in light level. The first experiment examined the time course of sensitivity to a small amplitude 1-s contrast pedestal presented on a 163-td pedestal within a 115-td surround. The largest contrast pedestal was an 8% contrast change that changed the steady pedestal threshold by only 0.03 log unit. Thresholds increased by 0.6 log unit or more at both onset and offset, with a return to baseline within 100 ms. The increment and decrement thresholds showed different time courses. Increment thresholds were raised before pedestal onset and decrement thresholds were raised before pedestal offset. These data were interpreted to show that increment thresholds measured at onset and offset of a contrast pedestal accessed on-pathways and decrement thresholds accessed off-pathways. In the second experiment, we examined the time course of sensitivity using a Crawford paradigm. Observers were dark-adapted and sensitivity was measured before, during, and after a 0.5-s, 68-td pulse. Test stimuli were slightly biased in chromaticity and the observer reported the presence and the hue appearance of the test, allowing separate estimates of detection and hue identification. Thresholds increased during the pulse but showed only a minimal overshoot. The test sensitivity for detection was poorer than for hue identification in the dark, but detection and identification were similar during the pulse. These data suggest that thresholds during sizable luminance pulses are determined in the PC-pathway.

Adaptation, Ocular↗
PubMedDate not supplied

Photostimulator allowing independent control of rods and the three cone types.

This report describes a second-generation photostimulator with four primary lights that allows independent control of the stimulation of the four receptor types in the human eye. The new design uses LEDs (with light levels controlled by eight drivers that include voltage-to-frequency converters that provide 1-micros pulses at frequencies up to 250 kHz), with four center channels being combined by use of a fiber optic assembly, and likewise for four surround channels. Four fiber optic bundles are merged into a single bundle whose output is fed into a spatial homogenizer terminated by a diffuser. An interference filter is sandwiched between each LED and the fiber optic bundle. Two camera lenses collimate light from the diffusers, one for center and one for surround. The center-surround field configuration is formed by a photometric cube with a mirrored ellipse on the hypotenuse. A field lens places images of the diffusers in the plane of an artificial pupil. The fields are highly uniform. Following alignment and calibration, the center and surround fields are indistinguishable. An observer calibration procedure, designed to compensate for prereceptoral filtering, is shown by calculation to correct also for normal observer receptoral spectral sensitivity variation. With the instrument calibrated for the individual observer, a peripherally fixated 200-ms 40% contrast rod center field pulse, highly conspicuous under dark adaptation, is invisible following light adaptation.

Calibration↗
PubMedDate not supplied

Inferred retinal mechanisms mediating illusory distortions.

The Zoellner illusion is a geometric distortion occurring when nonorthogonal inducing lines appear to tilt veridically parallel bars. The retinal pathways contributing to such illusions are unknown. The goal of this experiment was to investigate the retinal origin of the illusion. This was accomplished by determining the contrast gain for illusion thresholds. The magnocellular (MC-) and parvocellular (PC-) pathways exhibit different contrast gains, and this difference can be used psychophysically to identify the pathway. The stimulus pattern was four vertical bars with a series of inducing lines. The bars were always 5% higher in contrast than the inducing bars. The pattern was presented on a larger pedestal. Two paradigms were used. In the pulsed-pedestal paradigm, the observer adapted to the background and the pedestal and pattern were presented together as a brief pulse. In the steady-pedestal paradigm, the observer adapted to the continuously presented pedestal and the pattern appeared as a brief pulse. The contrast between the pedestal and the pattern was varied to obtain thresholds for two criteria: perceiving the directions of the inner inducing lines, and perceiving the distortion of the bars. The results for both criteria were similar in shape, but displaced in sensitivity. Detection of the directions of the inner inducing lines was 0.16-0.29 log unit more sensitive than perception of the illusion. The data for the pulsed-pedestal paradigm depended on the contrast between the pedestal and the pattern and produced a shallow V-shape. These results were associated with mediation in the PC-pathway. The data for the steady-pedestal paradigm depended on the pedestal luminance in a linear relation and showed similar sensitivity to the data for the pulsed-pedestal paradigm. Perception of the illusion required 10-15% Weber contrast.

Adult↗
PubMedDate not supplied

Interactions of chromaticity and luminance in edge identification depend on chromaticity.

The goal of this work was to study interactions of chromaticity and luminance in edge identification. Two horizontal spatial sawtooth patterns, one with positive and the other with negative harmonics, were compared in a two-alternative forced-choice (2-AFC) procedure. The observer identified which pattern had sharp upper or lower edges. The fundamental frequency was 2 cycles/deg (cpd), with 5 cycles presented in a 2.5-deg square field. The pattern was presented as a 1-s raised temporal cosine, replacing part of an 8-deg background. Stimuli were specified in a cone troland (l, s, Y) chromaticity space, with correction for individual equiluminance at a nominal 115 td, and individual tritan direction. A preliminary set of interleaved staircases established edge identification for the six directions of the (l, s, Y) space. Three compound stimuli combining two orthogonal directions were chosen and included with the end-points in five randomly interleaved staircases. For combinations of Y with l-chromaticity, or l- with s-chromaticity, probability summation was observed. Combinations of Y with s-chromaticity revealed opponency. Data for +s, +Y and -s, -Y were subadditive; data for +s, -Y and -s, +Y were additive. Control studies using detection rather than edge identification revealed probability summation for all combinations. Luminance edges did not enhance stimuli with l-chromaticities. There was an interaction of luminance edges with s-chromaticities. Dim "blues" and bright "yellows" showed linear summation. Bright "blues" and dim "yellows" showed opponency.

Choice Behavior↗
PubMedDate not supplied

Achromatic parvocellular contrast gain in normal and color defective observers: Implications for the evolution of color vision.

The PC pathway conveys both chromatic and achromatic information, with PC neurons being more responsive to chromatic (L-M) than to achromatic (L+M) stimuli. In considering the evolution of color vision, it has been suggested that the dynamic range of chromatic PC-pathway processing is tuned to the chromatic content of the natural environment. Anomalous trichromats, with reduced separation of their L- and M-cone spectral sensitivities, have diminished chromatic input to PC-pathway cells. Dichromats, with absent L or M cones, should have no chromatic input to PC-pathway cells. Therefore, the PC-pathway dynamic range of color defectives should be released from any constraint imposed by the chromatic environment. Here we ask whether this results in compensatory enhancement of achromatic PC-pathway processing in color defectives. This study employed a psychophysical method designed to isolate PC-pathway processing using achromatic stimuli. In a pulsed-pedestal condition, a four-square stimulus array appeared within a uniform surround. During a trial, one of the test squares differed from the other three, and the observer's task was to choose the square that was different. A four-alternative, forced-choice method was used to determine thresholds as a function of the contrast of the four-square array to the surround. Seven color defective and four normal observers participated. Results showed no systematic differences between normals and color defectives. There was no enhancement of achromatic processing as compensation for reduced chromatic processing in the PC-pathway system in color defectives. From physiological recordings, PC-pathway achromatic contrast gains of dichromatic and trichromatic New World primates and trichromatic Old World macaques have also been shown to be similar to each other. Our study and the animal studies imply that PC-pathway contrast gain parameters were regulated by factors other than the environmental chromaticity gamut, and may have arisen in a nontrichromatic common ancestor to both Old and New World primates.

Animals↗
PubMedDate not supplied

Dark-adapted rod suppression of cone flicker detection: Evaluation of receptoral and postreceptoral interactions.

Dark-adapted rods in the area surrounding a luminance-modulated field can suppress flicker detection. However, the characteristics of the interaction between rods and each of the cone types are unclear. To address this issue, the effect that dark-adapted rods have on specific classes of receptoral and postreceptoral signals was determined by measuring the critical fusion frequencies (CFF) for receptoral L-, M-, and S-cone and postreceptoral luminance ([L+M+S] and [L+M+S+Rod]) and chromatic ([L/(L+M)]) signals in the presence of different levels of surrounding rod activity. Stimuli were generated with a two-channel photostimulator that has four primaries for a central field and four primaries for the surround, allowing independent control of rod and cone excitation. Measurements were made either with adaptation to the stimulus field after dark adaptation or during a brief period following light adaptation. The results show that dark-adapted rods maximally suppressed the CFF by approximately 6 Hz for L-cone, M-cone, and luminance modulation. Dark-adapted rods, however, did not significantly alter the S-cone CFF. The [L/(L+M)] postreceptoral CFF was slightly suppressed at higher surround illuminances, that is, higher than surround luminances resulting in suppression for L-cone, M-cone, or luminance modulation. We conclude that rod-cone interactions in flicker detection occurred strongly in the magnocellular pathway.

Color Perception↗
PubMedDate not supplied

Spatial and temporal chromatic contrast: Effects on chromatic discrimination for stimuli varying in L- and M-cone excitation.

Discrimination for equiluminant chromatic stimuli that vary in L- and M-cone excitation depends on the chromaticity difference between the test field and the surrounding area. The current study investigated the effect of the proximity in space and time of a surround to the test field on chromatic contrast discrimination. The experimental paradigm isolated spatial, temporal, and spatial-and-temporal chromatic contrast effects on discrimination. Chromatic contrast discrimination thresholds were assessed by a four-alternative spatial forced-choice procedure. Stimuli were either metameric to the equal energy spectrum, or varied in L-cone activation along a line of constant S-cone activation. A model based on primate parvocellular pathway physiology described the data. Spatial and temporal contrast produced equivalent reductions in chromatic discriminability as the chromatic difference between the test and surround increased. For all test chromaticities, discrimination was best in the absence of chromatic contrast. Chromatic contrast discrimination is determined by either the spatial or temporal contrast component of the signal.

Color Perception↗