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Y Albeck

Publications and source records attributed to Y Albeck.

7 recordsLinked to original sources

Effects of interaural decorrelation on neural and behavioral detection of spatial cues.

The detection of interaural time differences (ITDs) for sound localization critically depends on the similarity between the left and right ear signals (interaural correlation). We show that, like humans, owls can localize phantom sound sources well until the correlation declines to a very low value, below which their performance rapidly deteriorates. Decreasing interaural correlation also causes the response of the owl's tectal auditory neurons to decline nonlinearly, with a rapid drop followed by a more gradual reduction. A detection-theoretic analysis of the statistical properties of neuronal responses could account for the variance of behavioral responses as interaural correlation is decreased. Finally, cross-correlation analysis suggests that low interaural correlations cause misalignment of cross-correlation peaks across different frequencies, contributing heavily to the nonlinear decline in neural and ultimately behavioral performance.

Animals↗

Inhibition sensitive to interaural time difference in the barn owl's inferior colliculus.

In spontaneously active neurons in the external nucleus of the inferior colliculus of the barn owl, a stimulus-driven discharge was followed by a quiescent period lasting tens of milliseconds before the spontaneous activity resumed. The more favorable the interaural time difference, the longer the quiet period. The duration of the quiescent period also depended on stimulus frequency. Frequencies different from the neuron's best frequency induced shorter quiescent periods, although they could elicit similar rates of impulses. Also, the duration of the quiescent period was independent of interaural intensity difference. Thus, the quiet period is not due to an after-hyperpolarization but was an inhibitory effect that depended on the activity of other neurons. In some neurons, discharge continued after the stimulus without a quiescent period and gradually decayed over a period of 50-100 ms past the stimulus offset. The similarity between the quiescent period of the neurons mentioned above and the time course of the poststimulus discharge in these neurons suggests that these neurons serve as inhibitory interneurons.

Acoustic Stimulation↗

Tolerance to sound intensity of binaural coincidence detection in the nucleus laminaris of the owl.

Neurons of the owl's nucleus laminaris serve as coincidence detectors for measurement of interaural time difference. The discharge rate of nucleus laminaris neurons for both monaural and binaural stimulation increased with sound intensity until they reached an asymptote. Intense sounds affected neither the ratio between binaural and monaural responses nor the interaural time difference for which nucleus laminaris neurons were selective. Theoretical analysis showed that high afferent discharge rates cause coincidence detectors with only excitatory input to lose their selectivity for interaural time difference when coincidence of impulses from the same side becomes as likely as that of impulses from the two sides. We hypothesize that inhibitory input whose strength increases with sound intensity protects nucleus laminaris neurons from losing their sensitivity to interaural time difference with intense sounds.

Acoustic Stimulation↗

Responses of neurons in the auditory pathway of the barn owl to partially correlated binaural signals.

1. Extracellular single-unit recording in anesthetized barn owls was used to study neuronal response to dichotic stimuli of variable binaural correlation (BC). Recordings were made in the output fibers of nucleus laminaris (NL), the anterior division of the ventral lateral lemniscal nucleus (VLVa), the core of the central nucleus of the inferior colliculus (ICcC), the lateral shell of the central nucleus of the inferior colliculus (ICcLS), and the external nucleus of the inferior colliculus (ICx). 2. The response of all neurons sensitive to interaural time difference (ITD) varied with BC. The relationship between BC and impulse number fits a linear, a parabolic, or a ramp model. A linear or parabolic model fits most neurons in low-level nuclei. Higher order neurons in ICx did not respond to noise bursts with strong negative binaural correlation, creating a ramp-like response to BC. 3. A neuron's ability to detect ITD varied as a function of BC. Conversely, a neuron's response to BC changed with ITD. Neurons in NL, VLVa, and ICcC show almost periodic ITD response curves. In these neurons peaks and troughs of ITD response curves diminished as BC decreased, creating a flat ITD response when BC = 0. When BC was set to -1, the most favorable ITD became the least favorable one and vice versa. The ITD response curve of ICx neurons usually has a single dominant peak. The response of those neurons to a negatively correlated noise pair (BC = -1) showed two ITD peaks, flanking the position of the primary peak. 4. The parabolic BC response of NL neurons fits the prediction of the cross-correlation model, assuming half-wave rectification of the sound by the cochlea. Linear response is not predicted by the model. However, the parabolic and the linear neurons probably do not belong to two distinct groups as the difference between them is not statistically significant. Thus, the cross-correlation model provides a good description of the binaural response not only in NL but also in VLVa and ICcC. 5. Almost all ramp neurons occurred in either ICx or ICcLS where neurons are more broadly tuned to frequency than those in the lower nuclei. The synthesis of this response type requires, however, not only the convergence of different frequency channels but also inhibition between different ITD channels. We modeled the ramp response as a three-step process. First, different spectral channels converge to create broad frequency tuning. The response to variation in BC will be linear (or parabolic) because it is a sum of linear (parabolic) responses. Second, the activity in some adjacent ITD channels is subtracted by lateral inhibition. Finally, the result is rectified using a high threshold to avoid negative activity.

Acoustic Stimulation↗

Temporal structure model of binaural masking level difference.

It is shown that a simple cross-correlation model is not adequate to explain both binaural masking level difference (MLD) and spatial selective attention. The reason is that for a low-intensity signal in NoS(pi) condition the maximal activity in the binaural analyzer as a function of interaural delay in single spectral channel is independent of signal intensity. On the other hand, if detection ability is associated with the isolation of tonically firing units, MLD is simply explained as the increase in firing synchronization as a function of the signal's interaural phase difference (IPD). Quantitatively results are presented based on numerical solutions of the model.

Attention↗

The storage and recall of auditory memory.

The architecture of the auditory memory is investigated. The auditory information is assumed to be represented by f-t patterns. With the help of a psycho-physical experiment it is demonstrated that the storage of these patterns is highly folded in the sense that a long signal is broken into many short stretches before being stored in the memory. Recognition takes place by correlating newly heard input in the short term memory to information previously stored in the long term memory. We show that this correlation is performed after the input is accumulated and held statically in the short term memory.

Auditory Perception↗