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The eyes play an essential role in social communication. Eyeblinks, however, have thus far received minor attention. We previously showed that subjects blink in synchrony while viewing the same video stories (Nakano et al. in Proc R Soc B 276:3635–3644, ). We therefore hypothesized that eyeblinks are synchronized between listener and speaker in face-to-face conversation. Here, we show that listeners blinked with a delay of 0.25–0.5 s after the speaker blinked when the listeners viewed close-up video clips (with sound) of the speaker’s face. Furthermore, this entrainment was selectively triggered by speaker’s eyeblinks occurring at the end and during pauses in speech. Eyeblink entrainment was not observed when viewing identical video clips without sound, indicating that blink entrainment was not an automatic imitation. We therefore suggest that eyeblink entrainment reflects smooth communication between interactants. [ABSTRACT FROM AUTHOR]

umulated evidence shows that a subjective time interval is lengthened by preceding or concurrent presentation of flickers or repetitive tone stimuli that have been hypothesized to increase the frequency of pulse generation by a brain pacemaker. In the present study, we presented a series of repetitive tone stimuli after an interval that started and ended with tone markers. We found that subjective perception of the preceding interval was not lengthened but shortened by the tone stimuli that followed the interval. The perceived duration decreased as the frequency of the repetitive tone stimuli increased. The effect disappeared when the repetitive tone stimuli were delivered with a delay of 500 msec after the test interval or when continuous sound was delivered instead of delivering a rapid series of tones. On the basis of the results, we propose that the pulse count accumulated during a test interval was normalized by the clock frequency just after the test interval in a postdictive manner. [ABSTRACT FROM AUTHOR]

It is essential to sense anticipated and elapsed time in our daily life. Several areas of the brain including parietal cortex, prefrontal cortex, basal ganglia and olivo-cerebellar system are known to be related to this temporal processing. We now describe a number of cells in the supplementary eye field (SEF) with phasic, delay activity and postdelay activity modulation that varied with the length of the delay period. This variation occurred in two manners. First, cells became active with the shorter delay periods (GO signal presented earlier). We call these cells “short-delay cells”. Second, cells became active with the longer delay periods (GO signal presented later). We call these cells “long-delay cells”. However, such changed neuronal activity did not correlate with reaction time. These results suggest that the delay-dependent activity may reflect anticipated and elapsed time during performance of a delayed saccadic eye movement. [ABSTRACT FROM AUTHOR]

Successive tactile stimuli, delivered one to each hand, are referred to spatial representation before they are ordered in time (Yamamoto and Kitazawa in Nat Neurosci 4:759–765 ). In the present study, we examined if this applies even when they are delivered unilaterally to fingers of a single hand. Tactile stimuli were delivered left-to-rightward relative to the body (2nd–3rd–4th) or in reverse with stimulus onset asynchrony of 100 ms. Simultaneously with the delivery of tactile stimuli, three of nine small squares arranged in a matrix of 3 × 3 were turned on as if they appeared near the tips of the fingers. Although subjects were instructed to ignore the visual stimuli and make a forced choice between the two orders of tactile stimuli, the correct-judgment probability depended on the direction of visual stimuli. It was greater than 95% when the direction of visual stimuli matched that of the tactile stimuli, but less than 50% when they were opposite to each other. When the right hand was rotated counterclockwise on the horizontal plane (90°) so that the fingers were pointing to the left, the preferred direction of visual stimuli that yielded the peak correct judgment was also rotated, although not to the full extent. These results show that subjects cannot be basing their tactile temporal order judgment solely on a somatotopic map, but rather on a spatial map on which both visual and tactile signals converge. [ABSTRACT FROM AUTHOR]

Because faces in portraits are depicted more frequently in a left rather than a right oblique (half-profile or 3/4) view, we addressed the question of whether people find it easier to recognize the left or right 3/4 view of a familiar person’s face. We examined the ability of 13 subjects to match familiar faces that were presented in either the left or right 3/4 view, with names that were presented either before or after the faces (face-name and name-face matching tasks, respectively). In both tasks, the subjects responded more rapidly to a left than to a right 3/4 view of the same face. This suggests that during face recognition the processing of information from faces that are presented in the left 3/4 view is dominant over the processing of right 3/4 views of familiar faces. [ABSTRACT FROM AUTHOR]

Errors in reaching produced by displacing the visual field with wedge prisms decrease with trials, even when the error is not revealed until the completion of the movement. To examine how much additional delay in visual feed-back the monkey can compensate for, the effects of delaying the visual error signals were studied by presenting the terminal visual images after one of five delays, ranging from 0 to 500 ms. Adaptation was fastest when the delay was 0 or 10 ms, decreased significantly with a delay as small as 50 ms and approached zero when the delay was 500 ms. The size of the after-effect decreased with the delay accordingly. The results indicate that prism adaptation in the monkey critically depends on the availability of visual information within 50 ms of completion of the movement. Comparing the results with those for humans, we suggest that monkey and human share a mechanism of adaptation with a short time window of 50 ms, but the monkey lacks another mechanism of adaptation that allows a visual delay of 500 ms or more in humans. [ABSTRACT FROM AUTHOR]

The errors in target-reaching that are produced by laterally displacing vision with wedge prisms decrease with trials (prism adaptation). When the prisms are removed, errors in the opposite direction are observed (aftereffect). We investigated the size of the aftereffect 24 h and 72 h after a monkey had adapted to a visual displacement (30 mm), with rapid reaching movements. The aftereffect more than half of the size of the displacement was observed when the effect was tested immediately after the monkey had been exposed to the displacement for 50 trials. In contrast, the aftereffect was not observed at 24 h even when the monkey had been exposed to the displacement for 250 trials. However, when the monkey had been exposed for 500 trials, significant aftereffects more than half of the size of the displacement were observed at 24 h and 72 h. When both arms were adapted to opposite prism displacements, the long-lasting aftereffect was further shown to be specific for the arm used during the exposure. The results indicate that the aftereffects of prism adaptation last for at least 3 days, though more than 200 trials of additional repetition are required to consolidate the short-term effects into long-lasting ones. [ABSTRACT FROM AUTHOR]

How does the brain order successive events? Here we studied whether temporal order of two stimuli delivered in rapid succession, one to each hand, is determined before or after the stimuli are localized in space. When their arms were crossed, subjects could accurately report the temporal order, even when the interval between stimuli was as short as 70 ms. In most trials, subjects could also judge temporal order when their arms were crossed, but only if given adequate time (>1 s). At moderately short intervals (<300 ms), crossing the arms caused misreporting (that is, inverting) of the temporal order. Thus, at these intervals, the determining factor of temporal order was the spatial location of the hands. We suggest that it is not until the spatial locations of the hands are taken into account that the cutaneous signals from the respective hands are ordered in time. [ABSTRACT FROM AUTHOR]

Presents research which recorded the activity of Purkinje cells from the hemisphere of cerebellar lobules IV-VI in monkeys. Complex spikes discharged from Purkinje cells; Role of spikes in arm movements and motor skills; Examination of complex-spike discharges in various activities; Complex spikes conveying multiple types of information.

Human judgment of the temporal order of two sensory signals is liable to change depending on our prior experiences. Previous studies have reported that signals presented at short intervals but in the same order as the most frequently repeated signal are perceived as occurring simultaneously. Here we report opposite perceptual changes that conform* to a Bayesian integration theory in judging the order of two stimuli delivered one to each hand. [ABSTRACT FROM AUTHOR]

Focuses on the use of 'eye-blink' responses on laboratory studies in Great Britain. Relation between tone and shock; Principle of extinction; Inhibition of climbing fibers.

The development of long-term event memory in preverbal infants remains elusive. To address this issue, we applied an eye-tracking method that successfully revealed in great apes that they have long-term memory of single events. Six-, 12-, 18- and 24-month-old infants watched a video story in which an aggressive ape-looking character came out from one of two identical doors. While viewing the same video again 24 hours later, 18- and 24-month-old infants anticipatorily looked at the door where the character would show up before it actually came out, but 6- and 12-month-old infants did not. Next, 12-, 18- and 24-month-old infants watched a different video story, in which a human grabbed one of two objects to hit back at the character. In their second viewing after a 24-hour delay, 18- and 24-month-old infants increased viewing time on the objects before the character grabbed one. In this viewing, 24-month-old infants preferentially looked at the object that the human had used, but 18-month-old infants did not show such preference. Our results show that infants at 18 months of age have developed long-term event memory, an ability to encode and retrieve a one-time event and this ability is elaborated thereafter. [ABSTRACT FROM AUTHOR]

When we touch something with a tool, we feel the touch at the tip of the tool, rather than at the hand that holds the tool. Here we show that the judgment of the temporal order of two successive stimuli, delivered to the tips of sticks held in each hand, was dramatically altered by crossing the sticks without changing the positions of the hands, where the actual mechanoreceptors are located. This provides experimental evidence for the referral of tactile signals to the tip of a tool in the hand. [ABSTRACT FROM AUTHOR]

When typical adults watch TV programs, they show surprisingly stereo-typed gaze behaviours, as indicated by the almost simultaneous shifts of their gazes from one face to another. However, a standard saliency model based on low-level physical features alone failed to explain such typical gaze behaviours. To find rules that explain the typical gaze behaviours, we examined temporo-spatial gaze patterns in adults while they viewed video clips with human characters that were played with or without sound, and in the forward or reverse direction. We here show the following: 1) the 'peak' face scanpath, which followed the face that attracted the largest number of views but ignored other objects in the scene, still retained the key features of actual scanpaths, 2) gaze behaviours remained unchanged whether the sound was provided or not, 3) the gaze behaviours were sensitive to time reversal, and 4) nearly 60% of the variance of gaze behaviours was explained by the face saliency that was defined as a function of its size, novelty, head movements, and mouth movements. These results suggest that humans share a face-oriented network that integrates several visual features of multiple faces, and directs our eyes to the most salient face at each moment. [ABSTRACT FROM AUTHOR]