Keizo Shinomori

Senescence of the temporal impulse response to a luminous pulse

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.

Aging of human short-wave cone pathways

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.

Impulse response of an S-cone pathway in the aging visual system

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.

Color constancy of color-deficient observers under illuminations defined by individual color discrimination ellipsoids

We explored the color constancy mechanisms of color-deficient observers under red, green, blue, and yellow illuminations. The red and green illuminations were defined individually by the longer axis of the color discrimination ellipsoid measured by the Cambridge Colour Test. Four dichromats (3 protanopes and 1 deuteranope), two anomalous trichromats (2 deuteranomalous observers), and five color-normal observers were asked to complete the color constancy task by making a simultaneous paper match under asymmetrical illuminations in haploscopic view on a monitor. The von Kries adaptation model was applied to estimate the cone responses. The model fits showed that for all color-deficient observers under all illuminations, the adjustment of the S-cone response or blue-yellow chromatically opponent responses modeled with the simple assumption of cone deletion in a certain type (S-M, S-L or S-(L+M)) was consistent with the principle of the von Kries model. The degree of adaptation was similar to that of color-normal observers. The results indicate that the color constancy of color-deficient observers is mediated by the simplified blue-yellow color system with a von Kries-type adaptation effect, even in the case of brightness match, as well as by a possible cone-level adaptation to the S-cone when the illumination produces a strong S-cone stimulation, such as blue illumination.

Discrimination thresholds of normal and anomalous trichromats: Model of senescent changes in ocular media density on the Cambridge Colour Test.

Age-related changes in chromatic discrimination along dichromatic confusion lines were measured with the Cambridge Colour Test (CCT). One hundred and sixty-two individuals (16 to 88 years old) with normal Rayleigh matches were the major focus of this paper. An additional 32 anomalous trichromats classified by their Rayleigh matches were also tested. All subjects were screened to rule out abnormalities of the anterior and posterior segments. Thresholds on all three chromatic vectors measured with the CCT showed age-related increases. Protan and deutan vector thresholds increased linearly with age while the tritan vector threshold was described with a bilinear model. Analysis and modeling demonstrated that the nominal vectors of the CCT are shifted by senescent changes in ocular media density, and a method for correcting the CCT vectors is demonstrated. A correction for these shifts indicates that classification among individuals of different ages is unaffected. New vector thresholds for elderly observers and for all age groups are suggested based on calculated tolerance limits.

Spatial Correspondence Learning is Critical for the Sequence Effects of Symbolic Cueing

Attention orienting has been found to be influenced by the previous cueing status in a spatial cueing paradigm. The purpose of this study was to determine whether the cue predictive values or the spatial correspondence learning between cues and targets could influence the sequence effect of symbolic cueing. The findings revealed that the predictive values of arrow or word cues do not lead to different sequence effects, but that visually asymmetrical letter cues, which allow spatial correspondence learning between cues and targets, induce stronger sequence effects than visually symmetrical letter cues. In addition, visually symmetrical directional word cues can induce sequence effects. The results suggest that spatial correspondence learning, although not obligatory, is critical for the sequence effects of symbolic cueing. The findings support the feature-integration hypothesis, rather than the strategic adjustments account.

Amplitude difference and similar time course of impulse responses in positive- and negative-contrast detection.

Temporal impulse response functions (IRFs) were measured to investigate the temporal characteristics of positive- and negative-contrast detection in human vision. The IRFs were estimated using models from sequential double-pulse thresholds measured by the psi method. The results indicated that thresholds for positive contrast detection were significantly higher than those for negative contrast detection. However, positive- and negative-contrast IRFs were similar except for the first peak amplitude, reflecting the difference in sensitivity that originates from the summation operation rather than the linear filtering of the visual system.

The Output of Human Expression System Measured by Visual Adaptation and Its Implication for the Computer Recognition System

The better understanding of human face perception help to create the more intelligent computer system to recognize the expression in face. In this paper, we used the adaptation paradigm and Face Action Coding System (FACS) to model the output of the human expression system, we measured the expression aftereffect in the case that facial identity was not changed and in the case that facial identity was changed. The result revealed the significant influence from the facial identity system on the facial expression system, Based on the result, we discussed the theoretical implication for understanding the relationship between expression system and identity system and its implication for computer system to simulate the human behavior of expression recognition.

Sequence effects of the involuntary and the voluntary components of symbolic cueing

The orienting of attention has been found to be influenced by the previous cueing status in a spatial-cueing paradigm. The explanation for this sequence effect remains uncertain. This study separated the involuntary and the voluntary components of arrow cueing by manipulating the predicted target locations. For example, a left arrow cue may have indicated that the target was more likely to appear at the up location. Therefore, three trial types were repeated or switched between trials: cued (targets appeared along the direction of the arrows), predicted (targets appeared at the locations predicted by the arrows), and unrelated (targets appeared at the other two locations, neither cued nor predicted). RTs of cued trials were found to be significantly facilitated after a previous cued trial; however, the same effect was not observed for predicted trials. The results suggest that significant sequence effects are induced only in the involuntary component of arrow cueing. The findings support the feature-integration hypothesis for the sequence effect of symbolic cueing.

The Change of Expression Configuration Affects Identity-Dependent Expression Aftereffect but Not Identity-Independent Expression Aftereffect.

The present study examined the influence of expression configuration on cross-identity expression aftereffect. The expression configuration refers to the spatial arrangement of facial features in a face for conveying an emotion, e.g., an open-mouth smile vs. a closed-mouth smile. In the first of two experiments, the expression aftereffect is measured using a cross-identity/cross-expression configuration factorial design. The facial identities of test faces were the same or different from the adaptor, while orthogonally, the expression configurations of those facial identities were also the same or different. The results show that the change of expression configuration impaired the expression aftereffect when the facial identities of adaptor and tests were the same; however, the impairment effect disappears when facial identities were different, indicating the identity-independent expression representation is more robust to the change of the expression configuration in comparison with the identity-dependent expression representation. In the second experiment, we used schematic line faces as adaptors and real faces as tests to minimize the similarity between the adaptor and tests, which is expected to exclude the contribution from the identity-dependent expression representation to expression aftereffect. The second experiment yields a similar result as the identity-independent expression aftereffect observed in Experiment 1. The findings indicate the different neural sensitivities to expression configuration for identity-dependent and identity-independent expression systems.