Abstract
Single neurons in auditory cortex display highly selective spectrotemporal properties: their receptive fields modulate over small fractions of an octave and integrate across temporal windows of 100-200 ms. We investigated how these characteristics impact auditory behavior. Human observers were asked to detect a specific sound frequency masked by broadband noise; we adopted an experimental design which required the engagement of frequency-selective mechanisms to perform above chance. We then applied psychophysical reverse correlation to derive spectrotemporal perceptual filters for the assigned task. We were able to expose signatures of neuronal-like spectrotemporal tuning on a scale of 1/10 octave and 50-100 ms, but detailed modeling of our results showed that observers were not able to rely on the explicit output of these channels. Instead, human observers pooled from a large bank of highly selective channels via a weighting envelope poorly tuned for frequency (on a scale of 1.5 octave) with sluggish temporal dynamics, followed by a highly nonlinear max-like operation. We conclude that human detection of specific frequencies embedded within complex sounds suffers from a high degree of intrinsic spectrotemporal uncertainty, resulting in low efficiency values (<1 %) for this perceptual ability. Signatures of the underlying neural circuitry can be exposed, but there does not appear to be a direct line for accessing individual neural channels on a fine scale.
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