Abstract
The functional organization of human auditory cortex can be probed by characterizing responses to various classes of sound at different anatomical locations. Along with histological studies this approach has revealed a primary field in posteromedial Heschl's gyrus (HG) with pronounced induced high-frequency (70-150 Hz) activity and short-latency responses that phase-lock to rapid transient sounds. Low-frequency neural oscillations are also relevant to stimulus processing and information flow, however, their distribution within auditory cortex has not been established. Alpha activity (7-14 Hz) in particular has been associated with processesthat may differentially engage earlier versus later levels ofthe cortical hierarchy, including functional inhibition andthe communication of sensory predictions. These theories derive largely from the study of occipitoparietal sources readily detectable in scalp electroencephalography. To characterize the anatomical basis and functional significance of less accessible temporal-lobe alpha activity we analyzed responses to sentences in seven human adults (4 female) with epilepsy who had been implanted with electrodes in superior temporal cortex. In contrast to primary cortex in posteromedial HG, a non-primary field in anterolateral HG was characterized by high spontaneous alpha activity that was strongly suppressed during auditory stimulation. Alpha-power suppression decreased with distancefrom anterolateral HGthroughout superiortemporal cortex, andwasmore pronouncedfor clear comparedto degraded speech. This suppression could not be accounted for solely by a change in the slope of the power spectrum. The differential manifestation and stimulus-sensitivity of alpha oscillations across auditory fields should be accounted for in theories of their generation and function.
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Billig, A. J., Herrmann, B., Rhone, A. E., Gander, P. E., Nourski, K. V., Snoad, B. F., … Johnsrude, I. S. (2019). A sound-sensitive source of alpha oscillations in human non-primary auditory cortex. Journal of Neuroscience, 39(44), 8679–8689. https://doi.org/10.1523/JNEUROSCI.0696-19.2019
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