Tone detection thresholds in interaurally delayed noise of different bandwidths

Differences between the interaural phase of a noise and a target tone improve detection thresholds. The maximum masking release is obtained for detecting an antiphasic tone (Sπ) in diotic noise (N0). It has been shown in several studies that this benefit gradually declines as an interaural time delay (ITD) is applied to the noise. This decline has been attributed to the reduced interaural coherence of the noise. Here, we report detection thresholds for a 500 Hz tone in masking noise with ITDs up to 8 ms and bandwidths from 25 to 1000 Hz. Reducing the noise bandwidth from 100 to 50 and 25 Hz increased the masking release for 8-ms ITD, as expected for increasing temporal coherence with decreasing bandwidth. For bandwidths of 100–1000 Hz no significant difference in masking release was observed. Detection thresholds with these wider-band noises had an ITD dependence that is fully described by the temporal coherence imposed by the typical monaurally determined auditory-filter bandwidth. A binaural model based on interaural phase-difference fluctuations accounts for the data without using delay lines.

Spatial cue reliability drives frequency tuning in the barn Owl's midbrain

The robust representation of the environment from unreliable sensory cues is vital for the efficient function of the brain. However, how the neural processing captures the most reliable cues is unknown. The interaural time difference (ITD) is the primary cue to localize sound in horizontal space. ITD is encoded in the firing rate of neurons that detect interaural phase difference (IPD). Due to the filtering effect of the head, IPD for a given location varies depending on the environmental context. We found that, in barn owls, at each location there is a frequency range where the head filtering yields the most reliable IPDs across contexts. Remarkably, the frequency tuning of space-specific neurons in the owl's midbrain varies with their preferred sound location, matching the range that carries the most reliable IPD. Thus, frequency tuning in the owl's space-specific neurons reflects a higher-order feature of the code that captures cue reliability.

Emphasis of spatial cues in the temporal fine structure during the rising segments of amplitude-modulated sounds II: single-neuron recordings

Recently, with the use of an amplitude-modulated binaural beat (AMBB), in which sound amplitude and interaural-phase difference (IPD) were modulated with a fixed mutual relationship (Dietz et al. 2013b), we demonstrated that the human auditory system uses interaural timing differences in the temporal fine structure of modulated sounds only during the rising portion of each modulation cycle. However, the degree to which peripheral or central mechanisms contribute to the observed strong dominance of the rising slope remains to be determined. Here, by recording responses of single neurons in the medial superior olive (MSO) of anesthetized gerbils and in the inferior colliculus (IC) of anesthetized guinea pigs to AMBBs, we report a correlation between the position within the amplitude-modulation (AM) cycle generating the maximum response rate and the position at which the instantaneous IPD dominates the total neural response. The IPD during the rising segment dominates the total response in 78% of MSO neurons and 69% of IC neurons, with responses of the remaining neurons predominantly coding the IPD around the modulation maximum. The observed diversity of dominance regions within the AM cycle, especially in the IC, and its comparison with the human behavioral data suggest that only the subpopulation of neurons with rising slope dominance codes the sound-source location in complex listening conditions. A comparison of two models to account for the data suggests that emphasis on IPDs during the rising slope of the AM cycle depends on adaptation processes occurring before binaural interaction.