- Poster presentation
- Open Access
Neural coding of monaural and binaural intensity at low stimulus frequencies
© Bures and Marsalek 2015
- Published: 18 December 2015
- Sound Pressure Level
- Spike Train
- Auditory Nerve
- Spike Rate
- Stimulus Waveform
At low sound frequencies, spikes in the auditory nerve (AN) are phase-locked to the stimulus waveform. For sinusoidal stimuli, spike occurrences are restricted to the positive half-waves of the sound cycles, which constraints possible values of spike rates and their variability. As the spike rates are used for representation of sound intensity, the just noticeable differences (JNDs) of sound level and of inter-aural level difference (ILD) will be influenced. Due to the lack of appropriate AN data, we explore the topic using a computational model .
Another discrepancy of the modeling results with psychophysics is the simulated JND increasing with frequency, given a constant spike rate (Figure 1B), while psychophysical JNDs decrease with frequency. However, if we assume that maximum spike rate is in some way limited by the frequency (e.g., at most one spike can occur in each sound cycle) and that a given intensity range (e.g., 30 dB) is always mapped to the available range of spike rates (e.g., between zero and sound frequency), then the slope of the rate-intensity function increases and the JND decreases with frequency. The results show that intensity coding has specific properties at low sound frequencies, deserving more detailed electrophysiological studies than what is available in experimental literature today.
Funded by Institutional Support for Long-term Development of Research Organizations (PRVOUK) no. P 24 at the Charles University in Prague to P. M.
- Bures Z, Marsalek P: On the precision of neural computation with inter-aural level differences in the lateral superior olive. Brain Res. 2013, 1536: 16-26.PubMedView ArticleGoogle Scholar
- Ward LM, Davidson KP: Where the action is: Weber fractions as a function of sound pressure at low frequencies. J Acoust Soc Am. 1993, 94 (5): 2587-2594.PubMedView ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.