One of the goals of auditory neuroscience is to understand how speech and other natural sounds are analyzed and encoded in the human auditory cortex. One major finding is that perception and speech processing are crucially affected by temporal modulations in the acoustic signal. However, identifying in humans the physiological mechanisms that underlie the analysis of perceptually-relevant temporal modulations presents a considerable technical challenge. Extracellular recording methods are ideal for the investigation of time-based neural coding mechanisms, but they are typically limited to a single auditory area and cannot be generally used in human subjects. Magnetoencephalography (MEG) is a non-invasive tool, suitable for use in humans that records high-speed neural signals from the entire brain, though at the cost of significantly coarser spatial resolution. Fortunately, recent work has shown that investigations of the neural coding of acoustic modulations can indeed be conducted using MEG with human subjects. Thus MEG and extracellular recording can both be employed, in complementary ways, to investigate how temporal modulations are encoded by auditory cortex. The goal of this proposed research program is to understand how these acoustic modulations, the building blocks of speech and other natural sounds are encoded in auditory cortex. The acoustic modulations whose encoding is investigated are either embedded in a noisy background, as in a natural auditory scene, or modulated in both frequency and amplitude, independently and simultaneously, as in speech. The research program employs parallel sets of experiments: one set using MEG to record from human auditory cortex, and the other using extracellular recording methods in an animal model. With recordings from individual neurons, from the extracellular local field potential, and from the whole cortex, it may be possible to unify the different schemes used to neurally encode acoustic modulations, up and down the neural hierarchy.
Recent research suggests that a variety of hearing and cognitive impairments result from problems in temporal processing of sounds (e.g. developmental language disorders, and hearing impairment due to aging, auditory neuropathy, or cochlear implants). The present work will provide novel experimental approaches, as well as a rich empirical database on cortical temporal processing in normal human subjects, that can then be used in clinical settings.
|Cervantes Constantino, Francisco; Simon, Jonathan Z (2017) Dynamic cortical representations of perceptual filling-in for missing acoustic rhythm. Sci Rep 7:17536|
|Presacco, Alessandro; Simon, Jonathan Z; Anderson, Samira (2016) Effect of informational content of noise on speech representation in the aging midbrain and cortex. J Neurophysiol 116:2356-2367|
|Ding, Nai; Simon, Jonathan Z; Shamma, Shihab A et al. (2016) Encoding of natural sounds by variance of the cortical local field potential. J Neurophysiol 115:2389-98|
|Presacco, Alessandro; Simon, Jonathan Z; Anderson, Samira (2016) Evidence of degraded representation of speech in noise, in the aging midbrain and cortex. J Neurophysiol 116:2346-2355|
|Simon, Jonathan Z (2015) The encoding of auditory objects in auditory cortex: insights from magnetoencephalography. Int J Psychophysiol 95:184-90|
|Ding, Nai; Chatterjee, Monita; Simon, Jonathan Z (2014) Robust cortical entrainment to the speech envelope relies on the spectro-temporal fine structure. Neuroimage 88:41-6|
|Ding, Nai; Simon, Jonathan Z (2014) Cortical entrainment to continuous speech: functional roles and interpretations. Front Hum Neurosci 8:311|
|Xiang, Juanjuan; Poeppel, David; Simon, Jonathan Z (2013) Physiological evidence for auditory modulation filterbanks: cortical responses to concurrent modulations. J Acoust Soc Am 133:EL7-12|
|Ding, Nai; Simon, Jonathan Z (2013) Power and phase properties of oscillatory neural responses in the presence of background activity. J Comput Neurosci 34:337-43|
|Zion Golumbic, Elana M; Ding, Nai; Bickel, Stephan et al. (2013) Mechanisms underlying selective neuronal tracking of attended speech at a ""cocktail party"". Neuron 77:980-91|
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