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Figure 5C shows that taking into account the spike phase boosts the MI carried by the Spike count code or the Time-partitioned code alone (p < 10−12 for all 6 window sizes).

(A ) Spike times of a reward responsive (RR VTAA unit relative to hippocampal theta and raw LFP during running behavior, and spike phase distribution (circular concentration coefficient, kappa = 0.14; Rayleigh statistic p value = 0.002).

A high flow rate improved spike phase locking to gamma, whereas a low flow rate improved spike phase locking to beta.

Hence, the higher the flow rate was, the stronger the spike phase locking to gamma phase was.

Conversely, the lower the flow rate was, the stronger the spike phase locking to the beta phase was (Fig. 3A).

Finally, we observed that spike phase locking to LFP oscillations was also modified as a function of the flow rate condition (Fig. 3).

(B ) (Left panel) Spike phase-amplitude coupling: mean value for PING amplitude (defined as the number of Gi neurons spiking within a gamma burst) as a function of PINTH phase (defined from interpolation between successive theta bursts).

In particular, cellular odor-evoked activities, LFP oscillations and spike phase-locking to LFPs were strongly modified by nasal flow rate.

(Right panel) Spontaneous spike phase-frequency coupling: mean value for PING frequency (defined from the duration between successive gamma bursts) as a function of PINTH phase.

Spike-phase coherence analyses were then performed on the principal cell population.

Populations of interneurons exhibited strong spike-phase coherence to the rhythms present during odor sampling.