Average eye position aligned to EM onset. A, B, Mean horizontal eye trace, and C, D, mean vertical eye trace for MM1. E, F, Mean horizontal eye trace, and G, H, mean vertical eye trace for MM2. The solid red line plots mean eye position across all sessions and contrasts during VEM and V epochs; the dashed black lines show +/− SEM across the four electrodes stimulated. Traces have been aligned to EM onset (VEM) or the matching time in epochs without stimulation (V); total duration of FEF-EM is indicated by the lower, dark grey bar (250 ms). The upper, light grey bar indicates the period of visual stimulation (VEM, V); visual onset, at −133 ms relative to EM onset, is not shown. Any run showing a significant difference between the two conditions at any time point was removed (P > 0.05, corrected for multiple comparisons across time points; two sample, two-tailed t-test across all acquired trials). These mean traces from the remaining runs show no significant difference at the aggregate level.

Modulation of the contrast response function in area V1 by microstimulation of the FEF. A, Percent change in MR signal with respect to the baseline condition in the visual-only (V, black curve) and visual with FEF-EM (VEM, red curve) conditions as a function of luminance contrast. Each trace plots the mean response for all visual voxels localized in V1, from both subjects across all sessions. The fMRI data used to derive the area V4 curves was also used to derive the V4 curves presented in Fig. 5B of Ekstrom et al. (2008). The same holds true for the V4 data presented in Fig. 5A. B, Difference in fMRI activity between the VEM and V conditions at each contrast level (a subtraction of the two curves in A). Filled / hollow squares below the traces indicate a significant positive / negative interaction between the effects of EM and V on the activity (black symbols) (P < 0.05; two-way ANOVA). C, Fractional change in percent MR signal, (VEM — V)/V, indicating the effective change in fMRI activity caused by FEF-EM relative to the visual-only activation level. In all panels, error bars indicate 1 SEM across epochs; some error bars are smaller than the symbol used.

Contrast response functions for weakly and strongly visually driven voxels and their modulation by FEF microstimulation. A, Mean percent change in MR signal for the V conditions as a function of contrast, across both subjects and all visual voxels in the twelve visual areas defined in Figure 4. Areas with more active voxels are weighted more. V_all represents all visual voxels (P < 0.05, uncorrected). V_high represents the best visually driven voxels (P < 0.05, corrected). V_low represents all remaining voxels from the visual voxels pool not included in V_high (0.05, corrected < P < 0.05, uncorrected); on the cortical surface, these voxels are primarily located in annuli surrounding the best driven population. The smooth curves show the best fitting Naka-Rushton functions. B, Mean difference between VEM and V conditions. Filled / hollow squares below the traces indicate a significant positive / negative interaction between factors EM and V (P < 0.05; two-way ANOVA). C, Fractional change in percent MR signal. In all panels, error bars indicate 1 SEM across epochs.

Stimulus conditions, stimulus locations and localizer example. A, The ten stimulus conditions used: stimuli at five different luminance contrast levels, presented without (V) and with (VEM) simultaneous FEF-EM. 0% V was used as the baseline condition. The main visual effect at 50% contrast (see Materials and Methods) was used as a localizer to identify a common population of visual voxels for further analysis. B, C, Stimulus locations for MM1 and MM2, respectively. The stimuli were centered on the endpoint of the saccade vector produced by stimulating each electrode above the threshold needed to elicit a saccade. During a given fMRI session, we stimulated at 50% of this behaviorally-defined saccade threshold, using only one stimulus and electrode at a time. One stimulus example is shown in each panel, and the dotted white lines indicate the other stimulus positions used for that subject. The red dot in the center represents the fixation spot, which was visible in all conditions. D, A thresholded t-score map (P < 0.001, uncorrected) of the localizer contrast (50% VEM + 50%V versus 0% VEM + 0% V) overlaid on the flattened representation of occipital cortex from MM1. The results shown correspond to the representation of stimulus 3 in B. Sulci are dark grey, and white and black solid lines indicate representations of the vertical and horizontal meridians, respectively. Anatomical labels: Calc, Calcarine sulcus; CS, Central sulcus; IOS, Inferior Occipital sulcus; IPS, Intraparietal sulcus; LF, Lateral fissure; LuS, Lunate sulcus; OTS, Occipitotemporal sulcus; STS, Superior Temporal sulcus.

Contrast response functions in different visual areas. Percent change in MR signal with respect to the baseline, or 0% contrast, condition as a function of luminance contrast for twelve visual cortical areas, including: A, early visual areas V1, V2, V3 and V3A; B, ventral extrastriate areas V4, TEO (Temporal-occipital area) and TE (Temporal area); C, areas within the STS: MT (Middle Temporal area), MST (Medial Superior Temporal area) and FST (Fundus of Superior Temporal sulcus); and D, higher order areas LIP (Lateral Intraparietal area) and STP (Superior Temporal Polysensory area). See Materials and Methods for a full description of how areal borders were determined. Each trace plots the mean response for all visual voxels localized in a given area, from both subjects across all sessions (only one stimulus location was used in each session). The smooth curves show the best fitting Naka-Rushton function. Error bars indicate 1 SEM across epochs, and some error bars are smaller than the symbol used. Note that the x axis has a logarithmic scale, with a break between 0% and 3% contrast.

Modulation of contrast response functions in multiple visual areas by microstimulation of the FEF. A, B, C, The difference in fMRI activity between the VEM and V conditions at each contrast level (see Fig. 4B; area V1 is repeated here for comparative purposes) for the twelve areas defined in Figure 3. Filled / hollow squares below the traces indicate a significant positive / negative interaction between factors EM and V relative to the 0% values (P < 0.05; two-way ANOVA). D, E, F, Fractional change in percent MR signal [(VEM — V) / V]. In all panels, error bars indicate 1 SEM across epochs.

Schematic summary of the effect of FEF-EM. A, The concentric circles correspond to regions on the two-dimensional cortical surface representation of a visual stimulus (c.f. Fig. 1D). Red / blue match the well / less well driven populations of visual voxels in Figure 7. B, C, D, Projecting this surface to one dimension yields three different activity profiles, depending on the stimulus contrast used (solid curve represents visual-only activation, dotted curve the combined response to visual stimulation and FEF-EM).