Spatially Localized Time Shifts of the Perceptual Stream

Visual events trigger representations in different locations and times in the brain. In experience, however, these various neural responses refer to a single unified cause. To investigate how representations might be brought into temporal alignment, we attempted to locally manipulate neural processing in such a way that identical, simultaneous sequences would appear temporally misaligned. After adaptation to a 20 Hz sequentially expanding and contracting concentric grating, a running clock presented in the adapted region of the visual field appeared advanced relative to an identical clock presented simultaneously in an unadapted region. No such effect was observed following 5-Hz adaptation. Clock time reports following an exogenous cue showed the same effect of adaptation on perceived time, demonstrating that the apparent temporal misalignment was not mediated by differences in target selection or allocation of attention. This effect was not mediated by the apparent speed of the adapted clock: a clock in a 20-Hz-adapted spatial location appeared slower than a clock in a 5-Hz-adapted location, rather than faster. Furthermore, reaction times for a clock-hand orientation discrimination task were the same following 5- and 20-Hz adaptation, indicating that neural processing latencies were not differentially affected. Altogether, these findings suggest that the fragmented perceptual stream might be actively brought into temporal alignment through adaptive local mechanisms operating in spatially segregated regions of the visual field

Time dilation in dynamic visual display

How does the brain estimate time? This old question has led to many biological and psychological models of time perception (R. A. Block, 1989; P. Fraisse, 1963; J. Gibbon, 1977; D. L. I. Zakay, 1989). Because time cannot be directly measured at a given moment, it has been proposed that the brain estimates time based on the number of changes in an event (S. W. Brown, 1995; P. Fraisse, 1963; W. D. Poynter, 1989). Consistent with this idea, dynamic visual stimuli are known to lengthen perceived time (J. F. Brown, 1931; S. Goldstone & W. T. Lhamon, 1974; W. T. Lhamon & S. Goldstone, 1974, C. O. Z. Roelofs & W. P. C. Zeeman, 1951). However, the kind of information that constitutes the basis for time perception remains unresolved. Here, we show that the temporal frequency of a stimulus serves as the “clock” for perceived duration. Other aspects of changes, such as speed or coherence, were found to be inconsequential. Time dilation saturated at a temporal frequency of 4–8 Hz. These results suggest that the clock governing perceived time has its basis at early processing stages. The possible links between models of time perception and neurophysiological functions of early visual areas are discussed

Титульні сторінки та зміст

It has recently been shown that contact between one’s own limbs (self-touch) reduces the perceived intensity of pain, over and above the well-known modulation of pain by simultaneous colocalized tactile input Kammers et al. (Curr Biol 20:1819–1822, 2010). Here, we investigate how self-touch modulates somatosensory evoked potentials (SEPs) evoked by afferent somatosensory input. We show that the P100 SEP component, which has previously been implicated in the conscious perception of a tactile stimulus, is enhanced during self-touch, as compared to when one is touching nothing, an inanimate object, or another person. A follow-up experiment showed that there was no effect of self-touch on SEPs when the body parts in contact were not symmetric. Altogether, our findings suggest the interpretation that the secondary somatosensory cortex might underlie the specific analgesic effect of self-touch

The SSVEP tracks attention, not consciousness, during perceptual filling-in

Research on the neural basis of conscious perception has almost exclusively shown that becoming aware of a stimulus leads to increased neural responses. By designing a novel form of perceptual filling-in (PFI) overlaid with a dynamic texture display, we frequency-tagged multiple disappearing targets as well as their surroundings. We show that in a PFI paradigm, the disappearance of a stimulus and subjective invisibility is associated with increases in neural activity, as measured with steady-state visually evoked potentials (SSVEPs), in electroencephalography (EEG). We also find that this increase correlates with alpha-band activity, a well-established neural measure of attention. These findings cast doubt on the direct relationship previously reported between the strength of neural activity and conscious perception, at least when measured with current tools, such as the SSVEP. Instead, we conclude that SSVEP strength more closely measures changes in attention.</p

Expecting the unexpected : Temporal expectation increases the flash-grab effect

Acknowledgments EvH, TB, KC, and HH were supported by the Australian Government through the Australian Research Council's Discovery Projects funding scheme (project DP180102268). PC was supported by grants from Dartmouth College and from Natural Sciences and Engineering Research Council Canada.Peer reviewedPublisher PD

A search asymmetry for interocular conflict

When two different images are presented to the two eyes, the percept will alternate between the images (a phenomenon called binocular rivalry). In the present study, we investigate the degree to which such interocular conflict is conspicuous. By using a visual search task, we show that search for interocular conflict is near efficient (15 ms/item) and can lead to a search asymmetry, depending on the contrast in the display. We reconcile our findings with those of Wolfe and Franzel (1988), who reported inefficient search for interocular conflict (26 ms/item) and found no evidence for a search asymmetry. In addition, we provide evidence for the suggestion that differences in search for interocular conflict are contingent on the degree of abnormal fusion of the dissimilar images

How many motoric body representations can we grasp?

At present there is a debate on the number of body representations in the brain. The most commonly used dichotomy is based on the body image, thought to underlie perception and proven to be susceptible to bodily illusions, versus the body schema, hypothesized to guide actions and so far proven to be robust against bodily illusions. In this rubber hand illusion study we investigated the susceptibility of the body schema by manipulating the amount of stimulation on the rubber hand and the participant’s hand, adjusting the postural configuration of the hand, and investigating a grasping rather than a pointing response. Observed results showed for the first time altered grasping responses as a consequence of the grip aperture of the rubber hand. This illusion-sensitive motor response challenges one of the foundations on which the dichotomy is based, and addresses the importance of illusion induction versus type of response when investigating body representations

Spatially localised time shifts of the perceptual stream

Visual events trigger representations in different locations and times in the brain. In experience, however, these various neural responses refer to a single unified cause. To investigate how representations might be brought into temporal alignment, we attempted to locally manipulate neural processing in such a way that identical, simultaneous sequences would appear temporally misaligned. After adaptation to a 20 Hz sequentially expanding and contracting concentric grating, a running clock presented in the adapted region of the visual field appeared advanced relative to an identical clock presented simultaneously in an unadapted region. No such effect was observed following 5 Hz adaptation. Clock time reports following an exogenous cue showed the same effect of adaptation on perceived time, demonstrating that the apparent temporal misalignment was not mediated by differences in target selection or allocation of attention. This effect was not mediated by the apparent speed of the adapted clock: a clock in a 20-Hz-adapted spatial location appeared slower than a clock in a 5-Hz-adapted location, rather than faster. Furthermore, reaction times for a clock hand orientation discrimination task were the same following 5 Hz and 20 Hz adaptation, indicating that neural processing latencies were not differentially affected. Altogether, these findings suggest that the fragmented perceptual stream might be actively brought into temporal alignment through adaptive local mechanisms operating in spatially segregated regions of the visual field