Near-Real-Time Feature-Selective Modulations in Human Cortex

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Near-Real-Time Feature-Selective Modulations in Human Cortex Javier O. Garcia, Ramesh Srinivasan, John T. Serences  Current Biology  Volume 23, Issue 6, Pages 515-522 (March 2013) DOI: 10.1016/j.cub.2013.02.013 Copyright © 2013 Elsevier Ltd Terms and Conditions

Current Biology 2013 23, 515-522DOI: (10.1016/j.cub.2013.02.013) Copyright © 2013 Elsevier Ltd Terms and Conditions

Figure 1 Stimulus Protocol and SSVEP Response (A) Stimulus display: In the central location, a stream of letters was simultaneously presented with an oriented peripheral annulus on a uniform gray background. During the 3,000 ms trial, a target would appear as a shift in the orientation of the grating or an X or Y in the RSVP stream of letters. Subjects responded with a button press to the direction of the shift (clockwise/counterclockwise) or to the target letter (X orY). (B) Stimulus protocol: Stimuli were tagged with different flicker frequencies. The annulus was contrast reversed at 21.25 Hz, and the RSVP stream of letters was updated at rate of 12.1 Hz (50% duty cycle). (C) Mean of the SNR across subjects of the SSVEP responses to the flickering stimuli, calculated by dividing the power at the stimulus frequency (or the second harmonic of the stimulus frequency for the peripheral grating, see the Experimental Procedures) by the standard deviation of the surrounding frequencies, 6.7 Hz on each side of the stimulus frequency). Spatial distributions reflect a parietaloccipital response for the grating stimulus and a bilateral parietal response for the RSVP stimulus. See also Figure S5. Current Biology 2013 23, 515-522DOI: (10.1016/j.cub.2013.02.013) Copyright © 2013 Elsevier Ltd Terms and Conditions

Figure 2 Decoding and Encoding Orientation from the SSVEP Response (A) Linear discriminant classification results. For each subject, the SNR and phase of a subset of electrodes elements was used for the classification procedure, and the peak of the classification function was used as that subject’s classification performance (see Figure S4 and the Supplemental Experimental Procedures). The orientation of the grating could be decoded above chance (p < 0.05) based on the SSVEP response at 42.5 Hz (Figure 2A, blue bars), and decoding accuracy was higher when the grating was attended compared to when it was not attended. In contrast, the orientation of the peripheral grating could not be decoded based on the SSVEP response at 12.1Hz (red bars). The dotted line represents chance performance in this nine-way classification, and error bars represent the SEM across subjects. Asterisks indicate significant differences via a bootstrap procedure (see the Supplemental Experimental Procedures). (B) Diagnostic electrodes in the linear discriminant analysis across subjects: the color map of the topographic plot shows the probability that an electrode was used in the decoding analysis. The electrodes that contained the highest SNR (Figure 1C) were also the most diagnostic. (C) Basis set used in the forward encoding model, derived from half-sinusoidal functions raised to the sixth power (nine basis functions spanning 0°–160° in 20° steps). (D) Dynamic tuning functions derived using the forward encoding model based on SNR and phase angle of the SSVEP response before the target onset. The 12.1 Hz SSVEP response to the RSVP flicker does not produce tuned responses whereas the 42.5 Hz SSVEP response produces a tuned response that peaks at the angle of stimulus being viewed (which is 0° in this plot by convention). Error bars represent the SEM across subjects. (E) Average weight of the maximum channel response showing that the SNR of the parietal-occipital electrodes and, to a lesser extent the phase angle of the frontal electrodes, carries most of the orientation-selective information. See also Figures S4 and S7. Current Biology 2013 23, 515-522DOI: (10.1016/j.cub.2013.02.013) Copyright © 2013 Elsevier Ltd Terms and Conditions

Figure 3 Dynamic Tuning Functions (A) A wavelet decomposition of frequencies 5–50 Hz averaged across subjects and conditions. The lower plot shows a line plot of stimulus related responses (RSVP stream, 12.1Hz; oriented grating, 42.5Hz). (B–E) Forward encoding model results derived from a wavelet decomposition of the SSVEP response. With SNR and phase angle of the SSVEP response, locked to the target onset (500 ms before to 500 ms after), orientation response profiles were reconstructed as a function of time. Segregating trial types reveals differences between responses to attended stimuli (B) and unattended stimuli (C) and between correct trials (D) and incorrect trials (E). Gray planes mark time points of interest (200 ms before target onset, target onset, and target termination; see Figure 4). See also Figures S1–S3, S6, and S7. Current Biology 2013 23, 515-522DOI: (10.1016/j.cub.2013.02.013) Copyright © 2013 Elsevier Ltd Terms and Conditions

Figure 4 Dynamics of Reconstructed Orientation Channel Responses (A–C) Rotated view of Figure 3D (correct attended trials) (A). Each inset line plot shows the tuning functions derived from the time window 200 ms before target onset (B and C). These line plots display the effect of attention (B) and the effect of accuracy (C). Error bars represent the SEM across subjects, and significant differences between channel responses indicated by black bars on the x axis. (D) Normalized response in channels tuned 20° and −20°) separated by clockwise or counterclockwise target shifts. These responses show a shift in the response beginning 60 ms before target onset extending 400 ms after target onset. Significant divergence occurs between 165 and 255 ms after target onset (black bar on x axis). Current Biology 2013 23, 515-522DOI: (10.1016/j.cub.2013.02.013) Copyright © 2013 Elsevier Ltd Terms and Conditions