Akihiro Yagi

Awareness of Central Luminance Edge is Crucial for the Craik-O'Brien-Cornsweet Effect.

The Craik-O’Brien-Cornsweet (COC) effect demonstrates that perceived lightness depends not only on the retinal input at corresponding visual areas but also on distal retinal inputs. In the COC effect, the central edge of an opposing pair of luminance gradients (COC edge) makes adjoining regions with identical luminance appear to be different. To investigate the underlying mechanisms of the effect, we examined whether the subjective awareness of the COC edge is necessary for the generation of the effect. We manipulated the visibility of the COC edge using visual backward masking and continuous flash suppression while monitoring subjective reports regarding online percepts and aftereffects of adaptation. Psychophysical results showed that the online percept of the COC effect nearly vanishes in conditions where the COC edge is rendered invisible. On the other hand, the results of adaptation experiments showed that the COC edge is still processed at the early stage even under the perceptual suppression. These results suggest that processing of the COC edge at the early stage is not sufficient for generating the COC effect, and that subjective awareness of the COC edge is necessary.

Inhibitory tagging in visual search can be found if search stimuli remain visible.

Klein (1988) reported thatinhibitory tagging (i.e., inhibition of return in visual search) made reaction times for the detection of small probes increase at locations where there had previously been rejected items in serial visual search. It is reasonable that the attended and rejected locations are inhibited. However, subsequent studies did not support Klein’s idea. In these studies, inhibitory tagging was tested after removing the items from the search tasks. The paradigms in these studies were not appropriate for testing an object-based inhibitory effect because the objects (i.e., items) were removed from the display. In the present study, we found that evidence of inhibitory tagging could be observed only when the items of the search tasks were maintained until the responses for the small probes were made. This appeared to be an object-based effect.

Reduction of stimulus visibility compresses apparent time intervals

The neural mechanisms underlying visual estimation of subsecond durations remain unknown, but perisaccadic underestimation of interflash intervals may provide a clue as to the nature of these mechanisms. Here we found that simply reducing the flash visibility, particularly the visibility of transient signals, induced similar time underestimation by human observers. Our results suggest that weak transient responses fail to trigger the proper detection of temporal asynchrony, leading to increased perception of simultaneity and apparent time compression.

Visual signal detection and lambda responses

On the basis of the result in earlier studies that the lambda response was associated with offset of the saccade, e.g., onset of the fixation pause, the relationship between the lambda response and the visual information processing load was examined. Eleven subjects were presented simultaneously random patterns including visual signals on Goldman perimeter and tone pips including auditory signals at random. In the visual task, the subject was instructed to search on the random pattern and detect the visual signals. In the auditory task, he was instructed to listen to tone pips without ceasing eye movements and detect the tone signals. EEGs from Oz and Cz, and the vertical and the horizontal EOGs were recorded. The vector EOG was calculated from both EOGs for detecting the absolute value of the saccade size. The occipital EEGs time-locked to offset of saccades were averaged 100 times to obtain lambda responses. The vertex EEGs time-locked to tone signals were averaged 100 times to obtain vertex potentials to auditory stimuli (AEP). Amplitudes of the lambda response (NOP100 and P100-N180) in the visual task were significantly higher than in the auditory task. Amplitudes of AEP (N1 and N1-P2) in the auditory task were enhanced significantly more than in the visual task. The results showed that the lambda response varied with information-processing load. The lambda response can be applicable as an index of visual information processing in eye movement situations.

The pointedness effect on representational momentum

An observer’s memory for the final position of a moving object is shifted forward in the direction of that object’s motion. It is called representational momentum (RM). This study addressed stimulusspecific effects on RM. In Experiment 1, participants showed larger memory shift for an object moving in its typical direction of motion than when it moved in a nontypical direction of motion. In Experiment 2, participants indicated larger memory shift for a pointed pattern moving in the direction of its point than when it moved in the opposite direction. In Experiment 3, we again examined the influences of knowledge about object’s typical motions and the pointedness of objects, because we did not control the shape (pointedness) of objects in Experiment 1. The results showed that only pointedness affected the magnitude of memory shift and that the effect was smaller than the momentum effect.

Inhibitory Tagging on Randomly Moving Objects

Inhibitory tagging is a process that prevents focal attention from revisiting previously checked items in inefficient searches, facilitating search performance. Recent studies suggested that inhibitory tagging is object rather than location based, but it was unclear whether inhibitory tagging operates on moving objects. The present study investigated the tagging effect on moving objects. Participants were asked to search for a moving target among randomly and independently moving distractors. After either efficient or inefficient search, participants performed a probe detection task that measured the inhibitory effect on search items. The inhibitory effect on distractors was observed only after inefficient searches. The present results support the concept of object-based inhibitory tagging.

Comparison between the lambda response of eye-fixation-related potentials and the P100 component of pattern-reversal visual evoked potentials

The purpose of this study was to compare the lambda response of eye-fixation-related potentials (EFRPs) with the P100 component of pattern-reversal visual-evoked potentials. EFRPs were obtained by averaging EEGs time-locked to the offset of the saccade. The dipole of the lambda response and that of the P100 component were estimated by the dipole-tracing method (Musha & Homma, 1990). The locations of their dipoles at the occipital sites were very close to each other when the difference waveform, which was calculated by subtracting the EFRP to the patternless stimulus from the EFRP to the patterned stimulus, was used for the lambda response. This finding implies that the lambda response and P100 have a common neural generator in the visual cortex. However, the peak latency of the lambda response was shorter than that of P100. The saccades in the EFRP trial were considered to be the cause of the difference.

Larger forward memory displacement in the direction of gravity

An observers memory for the final position of a moving stimulus is shifted forward in the direction of its motion. Observers in an upright posture typically show a larger forward memory displacement for a physically downward motion than for a physically upward motion of a stimulus (representational gravity; Hubbard & Bharucha, 1988). We examined whether representational gravity occurred along the environmentally vertical axis or the egocentrically vertical axis. In Experiment 1 observers in either upright or prone postures viewed egocentrically upward and downward motions of a stimulus. Egocentrically downward effects were observed only in the upright posture. In Experiment 2 observers in either upright or prone postures viewed approaching and receding motions of a stimulus along the line of sight. Only in the prone posture did the receding motion produce a larger forward memory displacement than the approaching motion. These results indicate that representational gravity depends not on the egocentric axis but on the environmental axis.

Integrated effect of stimulation at fixation points on EFRP (eye-fixation related brain potentials)

The purpose of this study was to investigate the integrated effect of stimulation at the fixation points just before and just after saccadic eye-movement (saccade) on eye-fixation related brain potentials (EFRP: P75 and N105). Checkerboard patterns were used as stimuli. In Experiment 1, changes in check sizes between two fixation points enhanced the amplitude of P75, while changes in the phases of patterns between the two points did not affect EFRP. This result showed that EFRP was affected by two fixation points, and that changes in the retinal image between the two points did not necessarily affect EFRP. In Experiment 2, the relationship between EFRP and check size was investigated in detail. A second order relationship between logarithm of check size and the latency of P75, and a linear relationship between logarithm of check size and the amplitude of N105 were found. The effect of check size on the amplitude of P75 which might explain the increased amplitude of P75 observed in Experiment 1 did not appear. These results suggest that EFRP might reflect relative higher processing than peripheral stimulation at one fixation point.

Eye fixation related potentials in a proof reading task

The eye fixation related potential (EFRP) associated with the occurrence of fixation pauses can be obtained by averaging EEGs at termination of saccades. EFRP is a kind of ERP measurable at the eye movement situation. Variations of EFRP were examined during a proof reading task for a long time. Two paragraphs of sentences were presented on the left and the right sides of a CRT. The paragraph on one side had some irrelevant words. Ten subjects were asked to detect the irrelevant words. The task started at 09.20 h and finished at 16.00 h and consisted of five blocks. The duration of each block was 1-h task and 10-min rest including a lunch (70 min). EEG and EOG were recorded during the task. EEGs were averaged at termination of saccades to obtain EFRP. EFRP showed little changes during the morning blocks. However, the mean amplitude between 100 and 200 ms of the positive component in the last two blocks decreased significantly compared with other blocks. The error rate, the performance and the score of fatigue increased at the end of the task. EFRP would reflect decline of mental concentration (i.e. carelessness) caused by visual fatigue.