144 research outputs found
The role of perceptual learning on modality-specific visual attentional effects
No full textMorrone et al. [Morrone, M. C., Denti, V., & Spinelli, D. (2002). Color and luminance contrasts attract independent attention. Current Biology, 12, 1134-1137] reported that the detrimental effect on contrast discrimination thresholds of performing a concomitant task is modality specific: performing a secondary luminance task has no effect on colour contrast thresholds, and vice versa. Here we confirm this result with a novel task involving learning of spatial position, and go on to show that it is not specific to the cardinal colour axes: secondary tasks with red-green stimuli impede performance on a blue-yellow task and vice versa. We further show that the attentional effect can be abolished with continued training over 2-4 training days (2-20 training sessions), and that the effect of learning is transferable to new target positions. Given the finding of transference, we discuss the possibility that V4 is a site of plasticity for both stimulus types, and that the separation is due to a luminance-colour separation within this cortical area
The lowest spatial frequency channel determines brightness perception
No full textThis study investigates the role played by individual spatial scales in determining the apparent brightness of greyscale patterns. We measured the perceived difference in brightness across an edge in the presence of notch filtering and high-pass filtering for two stimulus configurations, one that elicits the perception of transparency and one that appears opaque. For both stimulus configurations, the apparent brightness of the surfaces delimited by the border decreased monotonically with progressive (ideal) high-pass filtering, with a critical cut-off at I c/deg. Using two octave ideal notch filtering, the maximum detrimental effect on apparent brightness was observed at about I c/deg. Critical frequencies for apparent brightness did not vary with contrast, viewing distance, or surface size, suggesting that apparent brightness is determined by the channel tuned at I c/deg. Modelling the data with the local energy model [Morrone, M. C., & Burr, D. C. (1988). Feature detection in human vision: a phase dependent energy model. Proceedings of the Royal Society (London), B235, 221-245] at I c/deg confirmed the suggestion that this channel mediates apparent brightness for both opaque and transparent borders, with no need for pooling or integration across spatial channels. (C) 2007 Elsevier Ltd. All rights reserved
Active movement restores veridical event-timing after tactile adaptation
No full textTomassini A, Gori M, Burr D, Sandini G, Morrone MC. Active movement restores veridical event-timing after tactile adaptation. J Neurophysiol 108: 2092-2100, 2012. First published July 25, 2012; doi: 10.1152/jn.00238.2012.-Growing evidence suggests that time in the subsecond range is tightly linked to sensory processing. Event-time can be distorted by sensory adaptation, and many temporal illusions can accompany action execution. In this study, we show that adaptation to tactile motion causes a strong contraction of the apparent duration of tactile stimuli. However, when subjects make a voluntary motor act before judging the duration, it annuls the adaptation-induced temporal distortion, reestablishing veridical event-time. The movement needs to be performed actively by the subject: passive movement of similar magnitude and dynamics has no effect on adaptation, showing that it is the motor commands themselves, rather than reafferent signals from body movement, which reset the adaptation for tactile duration. No other concomitant perceptual changes were reported (such as apparent speed or enhanced temporal discrimination), ruling out a generalized effect of body movement on somatosensory processing. We suggest that active movement resets timing mechanisms in preparation for the new scenario that the movement will cause, eliminating inappropriate biases in perceived time. Our brain seems to utilize the intention-to-move signals to retune its perceptual machinery appropriately, to prepare to extract new temporal information
Motor commands induce time compression for tactile stimuli.
No full textSaccades cause compression of visual space around the saccadic target, and also a compression of time, both phenomena thought to be related to the problem of maintaining saccadic stability (Morrone et al., 2005; Burr and Morrone, 2011). Interestingly, similar phenomena occur at the time of hand movements, when tactile stimuli are systematically mislocalized in the direction of the movement (Dassonville, 1995; Watanabe et al., 2009). In this study, we measured whether hand movements also cause an alteration of the perceived timing of tactile signals. Human participants compared the temporal separation between two pairs of tactile taps while moving their right hand in response to an auditory cue. The first pair of tactile taps was presented at variable times with respect to movement with a fixed onset asynchrony of 150 ms. Two seconds after test presentation, when the hand was stationary, the second pair of taps was delivered with a variable temporal separation. Tactile stimuli could be delivered to either the right moving or left stationary hand.Whenthe tactile stimuli were presented to the motor effector just before and during movement, their perceived temporal separation was reduced. The time compression was effector-specific, as perceived time was veridical for the left stationary hand. The results indicate that time intervals are compressed around the time of hand movements. As for vision, the mislocalizations of time and space for touch stimuli may be consequences of a mechanism attempting to achieve perceptual stability during tactile exploration of objects, suggesting common strategies within different sensorimotor systems
Spatiotopic selectivity of adaptation-based compression of event duration
No full textA. Bruno, I. Ayhan, and A. Johnston (2010) have recently challenged our report of spatiotopic selectivity for adaptation of event time (D. Burr, A. Tozzi, & M. C. Morrone, 2007) and also our claim that retinotopic adaptation of event time depends on perceived speed. To assist the reader judge this issue, we present here a mass of data accumulated in our laboratories over the last few years, all confirming our original conclusions. We also point out that where Bruno et al. made experimental measurements (rather than relying on theoretical reasoning), they too find clearly significant spatiotopically tuned adaptation-based compression of event time but of lower magnitude to ours. We speculate on the reasons for the differences in magnitude
Temporal impulse response functions for luminance and colour during saccades
No full textPrevious work has shown that during saccadic eye movements, contrast sensitivity for low spatial frequency patterns modulated in luminance is selectively reduced by up to one logarithmic unit, while high spatial frequency patterns, and equiluminant patterns of all spatial frequencies are not suppressed at all: [Burr et al. (1994). Nature, 371, 511-513]. Here we study the temporal characteristics for sensitivity to luminance and chromatic patterns during saccades, using the two-pulse summation technique. Sensitivity was measured for detecting two successive pulses as a function of stimulus-onset asynchrony, during normal viewing and during saccades, Impulse response functions were estimated from the summation data, for all conditions. For equiluminance, the functions were monophasic during normal viewing and saccades. For luminance modulation, the impulse response functions were di-phasic in both normal viewing and saccades. However, during saccades the impulse responses were faster in normal viewing. This result is consistent with the suggestion that saccadic suppression is mediated by contrast gain control mechanisms, known to occur in M-cells but not P-cells. Copyright (C) 1996, Published by Elsevier Science Ltd
Spatial maps for time and motion
No full textIn this article, we review recent research studying the mechanisms for transforming coordinate systems to encode space, time and motion. A range of studies using functional imaging and psychophysical techniques reveals mechanisms in the human brain for encoding information in external rather than retinal coordinates. This reinforces the idea of a tight relationship between space and time, in the parietal cortex of primates
Auditory-visual temporal discrimination: Evidence for usage of a temporal cross-correlator
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