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Jason Samaha

Publications and source records attributed to Jason Samaha.

2 recordsLinked to original sources

How prior knowledge prepares perception: Prestimulus oscillations carry perceptual expectations and influence early visual responses.

Perceptual experience results from a complex interplay of bottom-up input and prior knowledge about the world, yet the extent to which knowledge affects perception, the neural mechanisms underlying these effects, and the stages of processing at which these two sources of information converge, are still unclear. In several experiments we show that language, in the form of verbal cues, both aids recognition of ambiguous \"Mooney\" images and improves objective visual discrimination performance in a match/non-match task. We then used electroencephalography (EEG) to better understand the mechanisms of this effect. The improved discrimination of images previously labeled was accompanied by a larger occipital-parietal P1 evoked response to the meaningful versus meaningless target stimuli. Time-frequency analysis of the interval between the cue and the target stimulus revealed increases in the power of posterior alpha-band (8-14 Hz) oscillations when the meaning of the stimuli to be compared was trained. The magnitude of the pre-target alpha difference and the P1 amplitude difference were positively correlated across individuals. These results suggest that prior knowledge prepares the brain for upcoming perception via the modulation of alpha-band oscillations, and that this preparatory state influences early (~120 ms) stages of visual processing.

Neuroscience

Preparatory encoding of the fine scale of human spatial attention

Our attentional focus is constantly shifting: in one moment our vision may be intently concentrated on a specific spot, while in another moment we might spread our attention more broadly. While much is known about the mechanisms by which we shift our visual attention from place to place, relatively little is know about how we shift the aperture of attention from more narrowly-to more broadly-focused. Here we introduce a novel attentional distribution task to examine the neural mechanisms underlying this process. In this task, participants are presented with an informative cue that indicates the location of an upcoming target. This cue can be perfectly predictive of the exact target location, or it can indicate--with varying degrees of certainty--approximately where the target might appear. This cue is followed by a preparatory period in which there is nothing on the screen except a central fixation cross. Using scalp EEG, we examined neural activity during this preparatory period. We find that with decreasing certainty regarding the precise location of the impending target, participant response times increased while target identification accuracy decreased. Additionally, N1 amplitude in response to the cue parametrically increased with spatial certainty while the multivariate pattern of preparatory period visual cortical alpha (8-12 Hz) activity encoded attentional distribution. Both of these electrophysiological parameters were predictive of behavioral performance nearly one second later. These results offer insight into the neural mechanisms underlying how we use information to guide our attentional distribution, and how that influences behavior.\n\nAuthors contributionsB.V. and A.G. conceived of the study; B.V. and A.G. designed the experimental task; B.V. and J.S. analyzed the EEG data; B.V., J.S., Z.G., N.G., S.P., T.K., S.R., and R.M. collected and analyzed behavioral data; all co-authors assisted in writing the manuscript.\n\nB.V. is funded by an NIH IRACDA (Institutional Research and Academic Career Development Award), a University of California Presidential Postdoctoral Fellowship, the University of California, San Diego CalIt2 Strategic Research Opportunities Program, and a Sloan Research Fellowship. A.G. is funded by the National Institutes of Health Grant R01-AG30395.\n\nSignificant StatementAnimals--including humans--frequently shift their visual attentional focus more narrowly or broadly depending on expectations. For example, a predator feline may focus their visual attention on a burrow hole, waiting for their prey to emerge. In contrast, a grizzly bear hunting salmon doesn't know precisely where the fish will jump out of the water, so it must spread its attention more broadly. In a series of novel experiments, we show that this broadening of attention comes at a behavioral cost. We find that multivariate changes in preparatory visual cortical oscillatory alpha (8-12 Hz) encode attentional distribution. These results shed light on the potential neural mechanisms by which preparatory information is used to guide attentional focus.

Neuroscience