SignificanceTheta rhythms, ≈3–8 Hz, have been found in many different parts of the brain. They are predominant in the rodent hippocampus, yet have also been described in the neocortex, primarily in frontal and parietal areas in relation to executive functions. Here, we show a ≈4-Hz theta rhythm in awake macaque monkey area V4 and primary visual cortex. This theta rhythm was spatially coextensive with visually induced gamma-band activity, and gamma power was modulated by theta phase. The strength of theta and of theta-rhythmic gamma modulation was markedly reduced by selective attention. Theta rhythmicity has been observed in microsaccade sequences, and microsaccades influence early visual activity. Yet, removing (the effects of) microsaccades did not influence the results.

Highlights d A distinct neuron type with thin spikes and high burst propensity in monkey V1 d These neurons are present in both Old World and New World monkeys, but not in mice d They show relatively strong gamma (30-80 Hz) rhythmicity and stimulus selectivity d Firing suppression contributes to their orientation tuning and gamma rhythmicity

Circuits of excitatory and inhibitory neurons generate gamma-rhythmic activity (30–80 Hz). Gamma-cycles show spontaneous variability in amplitude and duration. To investigate the mechanisms underlying this variability, we recorded local-field-potentials (LFPs) and spikes from awake macaque V1. We developed a noise-robust method to detect gamma-cycle amplitudes and durations, which showed a weak but positive correlation. This correlation, and the joint amplitude-duration distribution, is well reproduced by a noise-driven damped harmonic oscillator. This model accurately fits LFP power-spectra, is equivalent to a linear, noise-driven E-I circuit, and recapitulates two additional features of gamma: (1) Amplitude-duration correlations decrease with oscillation strength; (2) amplitudes and durations exhibit strong and weak autocorrelations, respectively, depending on oscillation strength. Finally, longer gamma-cycles are associated with stronger spike-synchrony, but lower spike-rates in both (putative) excitatory and inhibitory neurons. In sum, V1 gamma-dynamics are well described by the simplest possible model of gamma: A damped harmonic oscillator driven by noise.

No abstract

SUMMARYCircuits of excitatory and inhibitory neurons can generate rhythmic activity in the gamma frequency-range (30-80Hz). Individual gamma-cycles show spontaneous variability in amplitude and duration. The mechanisms underlying this variability are not fully understood. We recorded local-field-potentials (LFPs) and spikes from awake macaque V1, and developed a noise-robust method to detect gamma-cycle amplitudes and durations. Amplitudes and durations showed a weak but positive correlation. This correlation, and the joint amplitude-duration distribution, is well reproduced by a dampened harmonic oscillator driven by stochastic noise. We show that this model accurately fits LFP power spectra and is equivalent to a linear PING (Pyramidal Interneuron Network Gamma) circuit. The model recapitulates two additional features of V1 gamma: (1) Amplitude-duration correlations decrease with oscillation strength; (2) Amplitudes and durations exhibit strong and weak autocorrelations, respectively, depending on oscillation strength. Finally, longer gamma-cycles are associated with stronger spike-synchrony, but lower spike-rates in both (putative) excitatory and inhibitory neurons. In sum, V1 gamma-dynamics are well described by the simplest possible model of gamma: A linear harmonic oscillator driven by noise.