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Lance Nizami

Publications and source records attributed to Lance Nizami.

5 recordsLinked to original sources
PubMed2003

Afferent response parameters derived from postmasker probe-detection thresholds: 'the decay of sensation' revisited.

The classical model of forward masking postulates that the detection threshold for a tone probe that follows a stimulus of similar frequency content is elevated relative to the quiet threshold because the probe must evoke a just-detectable increment in a decaying postmasker sensation. That postmasker decay is charted by probe-detection thresholds if the sensation increment is small and constant. This model was examined for a 2-kHz Gaussian-shaped probe and a 2-kHz forward masker, based on the model's assumption that a just-detectable increment in sensation results from a just-detectable increment in level. Psychometric functions for detection were obtained at 2.5-30 ms postmasker. Their means and standard deviations generally decreased with delay. It was assumed that standard deviation is related to the putative just-detectable level increment by a simple monotonic transformation. Thus, if the standard deviation of the psychometric function for probe detection is neither small nor constant, then the corresponding just-detectable increment in level is neither small nor constant, and the just-detectable increment in sensation is neither small nor constant. The classical model also fails to allow for the variability of internal events. The concept of detection threshold as a sensation increment was preserved in a Signal Detection model, that does allow for internal variability. In this model the postmasker residual is the input to a probe detector. The new model produces an equation for the just-detectable level increment as a function of probe delay. Comparison data were generated by again assuming some relation between the standard deviation of the psychometric function for detection, and the just-detectable increment in level. The fit of equation to data yields robust values for the probe detector's maximum firing rate, dynamic range, and spike-counting time. All that is required to account for the decay of sensation, for a pure tone, is a single neuron operating at some higher center.

Animals↗
PubMed2003

Effects of peripheral nonlinearity on psychometric functions for forward-masked tones.

Psychometric functions (PFs) for forward-masked tones were obtained for conditions in which signal level was varied to estimate threshold at several masker levels (variable-signal condition), and in which masker level was varied to estimate threshold at several signal levels (variable-masker condition). The changes in PF slope across combinations of masker frequency, masker level, and signal delay were explored in three experiments. In experiment 1, a 2-kHz, 10-ms tone was masked by a 50, 70 or 90 dB SPL, 20-ms on-frequency forward masker, with signal delays of 2, 20, or 40 ms, in a variable-signal condition. PF slopes decreased in conditions where signal threshold was high. In experiments 2 and 3, the signal was a 4-kHz, 10-ms tone, and the masker was either a 4- or 2.4-kHz, 200-ms tone. In experiment 2, on-frequency maskers were presented at 30 to 90 dB SPL in 10-dB steps and off-frequency maskers were presented at 60 to 90 dB SPL in 10-dB steps, with signal delays of 0, 10, or 30 ms, in a variable-signal condition. PF slopes decreased as signal level increased, and this trend was similar for on- and off-frequency maskers. In experiment 3, variable-masker conditions with on- and off-frequency maskers and 0-ms signal delay were presented. In general, the results were consistent with the hypothesis that peripheral nonlinearity is reflected in the PF slopes. The data also indicate that masker level plays a role independent of signal level, an effect that could be accounted for by assuming greater internal noise at higher stimulus levels.

Adult↗
PubMed2002

Estimating auditory neuronal dynamic range using a fitted function.

To obtain the dynamic range of an auditory afferent, the neuron's firing rate is plotted versus stimulus level, and the dynamic range is taken as the difference between the threshold for evoked firing, and the level at which firing rate saturates. Those dynamic range endpoints are typically defined in terms of the neuron's spontaneous firing rate and its maximum firing rate, according to a plurality of schemes, each of which depends on user-chosen sets of numerical criteria. The dynamic ranges predicted by some of these schemes are compared for the first time, and the resulting estimates can differ by a factor of 2. A step can be taken towards standardizing the measurement of neuronal dynamic range, if dynamic range is incorporated into a rate-level function as a parameter. To build this function, it is first assumed that the neuron's rate-level response reaches half its maximum at a level half-way between the threshold and the level at saturation, i.e. at threshold plus half the dynamic range. Then the firing rates at threshold and at threshold plus dynamic range are defined according to the most popular of the endpoint schemes. The resulting equation produces credible estimates of neuronal properties when fitted, and correctly predicts the behavior of the slope of the empirical rate-level plot [McGee, 1983. M.S. thesis, Creighton University; Ohlemiller et al., 1991. J. Acoust. Soc. Am. 90, 274-287]. Thus, despite not being deterministic, the new equation has remarkable predictive power. When two of the rate-level functions are added and weighted, the resulting equation fits sloping-saturating data better than any functions presently employed.

Animals↗
PubMed2002

The mid-level hump at 2 kHz.

Shortening the duration of a Gaussian-shaped 2-kHz tone-pip causes the intensity-difference limen (DL) to depart from the "near-miss to Weber's law" and swell into a mid-level hump [Nizami et al., J. Acoust. Soc. Am. 110, 2505-2515 (2001)]. For some subjects the size of this hump approaches or exceeds the size reported for longer tones under forward masking, suggesting that forward masking might make little difference to the DL for very brief probes. To test this hypothesis, DLs were determined over 30 to 90 dB SPL for a brief Gaussian-shaped 2-kHz tone-pip. DLs were obtained first without forward masking, then with the pip placed 10 or 100 ms after a 200-ms 2-kHz tone of 50 dB SPL, or 100 ms after a 200-ms 2-kHz tone of 70 dB SPL. DLs inflated significantly under all forward-masking conditions. DLs also enlarged under an 80 dB SPL forward masker at pip delays of 4, 10, 40, and 100 ms. The peaks of the humps obtained under forward masking clustered around a sensation level (SL) that was significantly lower than the average SL for the peaks of the humps obtained without forward masking. Overall, the results do not support the neuronal-recovery-rate model of Zeng et al. [Hear. Res. 55, 223-230 (1991)], but are not incompatible with the Carlyon and Beveridge hypothesis [J. Acoust. Soc. Am. 93, 2886-2895 (1993)] that nonsimultaneous maskers corrupt the memory trace evoked by the probe.

Adult↗