Neural bases of rhythmic entrainment in humans: critical transformation between cortical and lower‐level representations of auditory rhythm

Abstract The spontaneous ability to entrain to meter periodicities is central to music perception and production across cultures. There is increasing evidence that this ability involves selective neural responses to meter‐related frequencies. This phenomenon has been observed in the human auditory cortex, yet it could be the product of evolutionarily older lower‐level properties of brainstem auditory neurons, as suggested by recent recordings from rodent midbrain. We addressed this question by taking advantage of a new method to simultaneously record human EEG activity originating from cortical and lower‐level sources, in the form of slow (< 20 Hz) and fast (> 150 Hz) responses to auditory rhythms. Cortical responses showed increased amplitudes at meter‐related frequencies compared to meter‐unrelated frequencies, regardless of the prominence of the meter‐related frequencies in the modulation spectrum of the rhythmic inputs. In contrast, frequency‐following responses showed increased amplitudes at meter‐related frequencies only in rhythms with prominent meter‐related frequencies in the input but not for a more complex rhythm requiring more endogenous generation of the meter. This interaction with rhythm complexity suggests that the selective enhancement of meter‐related frequencies does not fully rely on subcortical auditory properties, but is critically shaped at the cortical level, possibly through functional connections between the auditory cortex and other, movement‐related, brain structures. This process of temporal selection would thus enable endogenous and motor entrainment to emerge with substantial flexibility and invariance with respect to the rhythmic input in humans in contrast with non‐human animals.