SUMMARY Attending to a stimulus enhances its neuronal representation, even at the level of primary sensory cortex. Cross-modal modulation can similarly enhance a neuronal representation, and this process can also operate at the primary cortical level. Phase reset of ongoing neuronal oscillatory activity has been shown to be an important element of the underlying modulation of local cortical excitability in both cases. We investigated the influence of attention on oscillatory phase reset in primary auditory and visual cortices of macaques performing an intermodal selective attention task. In addition to responses “driven” by preferred modality stimuli, we noted that both preferred and non-preferred modality stimuli could “modulate” local cortical excitability by phase reset of ongoing oscillatory activity, and that this effect was linked to their being attended. These findings outline a supramodal mechanism by which attention can control neurophysiological context, thus determining the representation of specific sensory content in primary sensory cortex.

The functional significance of the ␣ rhythm is widely debated. It has been proposed that ␣ reflects sensory inhibition and/or a temporal sampling or "parsing" mechanism. There is also continuing disagreement over the more fundamental questions of which cortical layers generate ␣ rhythms and whether the generation of ␣ is equivalent across sensory systems. To address these latter questions, we analyzed laminar profiles of local field potentials (LFPs) and concomitant multiunit activity (MUA) from macaque V1, S1, and A1 during both spontaneous activity and sensory stimulation. Current source density (CSD) analysis of laminar LFP profiles revealed ␣ current generators in the supragranular, granular, and infragranular layers. MUA phase-locked to local current source/sink configurations confirmed that ␣ rhythms index local neuronal excitability fluctuations. CSD-defined ␣ generators were strongest in the supragranular layers, whereas LFP ␣ power was greatest in the infragranular layers, consistent with some of the previous reports. The discrepancy between LFP and CSD findings appears to be attributable to contamination of the infragranular LFP signal by activity that is volume-conducted from the stronger supragranular ␣ generators. The presence of ␣ generators across cortical depth in V1, S1, and A1 suggests the involvement of ␣ in feedforward as well as feedback processes and is consistent with the view that ␣ rhythms, perhaps in addition to a role in sensory inhibition, may parse sensory input streams in a way that facilitates communication across cortical areas.

Previous research demonstrated that while selectively attending to relevant aspects of the external world, the brain extracts pertinent information by aligning its neuronal oscillations to key time points of stimuli or their sampling by sensory organs. This alignment mechanism is termed oscillatory entrainment. We investigated the global, long-timescale dynamics of this mechanism in the primary auditory cortex of nonhuman primates, and hypothesized that lapses of entrainment would correspond to lapses of attention. By examining electrophysiological and behavioral measures we observed that besides the lack of entrainment by external stimuli, attentional lapses were characterized by high amplitude alpha oscillations, with alpha frequency structuring of neuronal ensemble and single unit operations. Strikingly, entrainment and alpha oscillation dominated periods were strongly anti-correlated and fluctuated rhythmically at an ultra-slow rate. Our results indicate that these two distinct brain states represent externally versus internally oriented computational resources engaged by large-scale task-positive and task-negative functional networks.

Recent electrophysiological and neuroimaging studies provide converging evidence that attending to sounds increases the response selectivity of neuronal ensembles even at the first cortical stage of auditory stimulus processing in primary auditory cortex (A1). This is achieved by enhancement of responses in the regions that process attended frequency content, and by suppression of responses in the surrounding regions. The goals of our study were to define the extent to which A1 neuronal ensembles are involved in this process, determine its effect on the frequency tuning of A1 neuronal ensembles, and examine the involvement of the different cortical layers. To accomplish these, we analyzed laminar profiles of synaptic activity and action potentials recorded in A1 of macaques performing a rhythmic intermodal selective attention task. We found that the frequency tuning of neuronal ensembles was sharpened due to both increased gain at the preferentially processed or best frequency and increased response suppression at all other frequencies when auditory stimuli were attended. Our results suggest that these effects are due to a frequency-specific counterphase entrainment of ongoing delta oscillations, which predictively orchestrates opposite sign excitability changes across all of A1. This results in a net suppressive effect due to the large proportion of neuronal ensembles that do not specifically process the attended frequency content. Furthermore, analysis of laminar activation profiles revealed that although attention-related suppressive effects predominate the responses of supragranular neuronal ensembles, response enhancement is dominant in the granular and infragranular layers, providing evidence for layer-specific cortical operations in attentive stimulus processing.

Broadband high-frequency activity (BHA; 70 to 150 Hz), also known as “high gamma,” a key analytic signal in human intracranial (electrocorticographic) recordings, is often assumed to reflect local neural firing [multiunit activity (MUA)]. As the precise physiological substrates of BHA are unknown, this assumption remains controversial. Our analysis of laminar multielectrode data from V1 and A1 in monkeys outlines two components of stimulus-evoked BHA distributed across the cortical layers: an “early-deep” and “late-superficial” response. Early-deep BHA has a clear spatial and temporal overlap with MUA. Late-superficial BHA was more prominent and accounted for more of the BHA signal measured near the cortical pial surface. However, its association with local MUA is weak and often undetectable, consistent with the view that it reflects dendritic processes separable from local neuronal firing.

SUMMARY Visual physiology is traditionally investigated by presenting stimuli with gaze held constant. However, during active viewing of a scene, information is actively acquired using systematic patterns of fixations and saccades. Prior studies suggest that during such active viewing, both nonretinal, saccade-related signals and “extra-classical” receptive field inputs modulate visual processing. This study used a set of active viewing tasks that allowed us to compare visual responses with and without direct foveal input, thus isolating the contextual eye movement-related influences. Studying nonhuman primates, we find strong contextual modulation in primary visual cortex (V1): excitability and response amplification immediately after fixation onset, transiting to suppression leading up to the next saccade. Time-frequency decomposition suggests that this amplification and suppression cycle stems from a phase reset of ongoing neuronal oscillatory activity. The impact of saccade-related contextual modulation on stimulus processing makes active visual sensing fundamentally different from the more passive processes investigated in traditional paradigms.

SignificanceOur results indicate that nonhuman primates detect complex repeating acoustic sequences in a continuous auditory stream, which is an important precursor for human speech learning and perception. We demonstrate that oscillatory entrainment, known to support the attentive perception of rhythmic stimulus sequences, can occur for rhythms defined solely by stimulus context rather than physical boundaries. As opposed to acoustically driven entrainment by rhythmic tone sequences demonstrated previously, this form of entrainment relies on the brain’s ability to group auditory inputs based on their statistical regularities. The internally initiated, context-driven modulation of excitability in the medial pulvinar prior to A1 supports the notion of top-down entrainment.

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