A computational technique is described for calculation of the inter-spike interval and poststimulus time histograms for the responses of an integrate-and-fire model to arbitrary inputs. The effects of the model parameters on the response statistics were studied systematically. Specifically, the probability distribution of the membrane potential was calculated as a function of time, and the mean interspike interval and PST histogram were calculated for arbitrary inputs. For stationary inputs, the regularity of the output was studied in detail for various model parameters. For nonstationary inputs, the effects of the model parameters on the output synchronization index were explored. The results show that enhanced synchronization in response to low-frequency stimuli required a large number ( n > 25) of weak inputs. Irregular responses and a linear input-output rate relationship required strong (but subthreshold) inputs with a small time constant. A model cell with mixed-amplitude synaptic inputs can respond to stationary inputs irregularly and have enhanced synchronization to nonstationary inputs that are phase-locked to low-frequency inputs. Both of these response properties have been reported for some cells in the ventral cochlear nucleus in the auditory brainstem.

Previous studies have combined analytical models of stochastic neural responses with signal detection theory (SDT) to predict psychophysical performance limits; however, these studies have typically been limited to simple models and simple psychophysical tasks. A companion article in this issue (“Evaluating Auditory Performance Limits: I”) describes an extension of the SDT approach to allow the use of computational models that provide more accurate descriptions of neural responses. This article describes an extension to more complex psychophysical tasks. A general method is presented for evaluating psychophysical performance limits for discrimination tasks in which one stimulus parameter is randomly varied. Psychophysical experiments often randomly vary a single parameter in order to restrict the cues that are available to the subject. The method is demonstrated for the auditory task of random-level frequency discrimination using a computational auditory nerve (AN) model. Performance limits based on AN discharge times ( all-information ) are compared to performance limits based only on discharge counts ( rate place ). Both decision models are successful in predicting that random-level variation has no effect on performance in quiet, which is the typical result in psychophysical tasks with random-level variation. The distribution of information across the AN population provides insight into how different types of AN information can be used to avoid the influence of random-level variation. The rate-place model relies on comparisons between fibers above and below the tone frequency (i.e., the population response), while the all-information model does not require such across-fiber comparisons. Frequency discrimination with random-level variation in the presence of high-frequency noise is also simulated. No effect is predicted for all-information, consistent with the small effect in human performance; however, a large effect is predicted for rate-place in noise with random-level variation.

A method for calculating psychophysical performance limits based on stochastic neural responses is introduced and compared to previous analytical methods for evaluating auditory discrimination of tone frequency and level. The method uses signal detection theory and a computational model for a population of auditory nerve (AN) fiber responses. The use of computational models allows predictions to be made over a wider parameter range and with more complete descriptions of AN responses than in analytical models. Performance based on AN discharge times ( all-information ) is compared to performance based only on discharge counts ( rate-place ). After the method is verified over the range of parameters for which previous analytical models are applicable, the parameter space is then extended. For example, a computational model of AN activity that extends to high frequencies is used to explore the common belief that rate-place information is responsible for frequency encoding at high frequencies due to the rolloff in AN phase locking above 2 kHz. This rolloff is thought to eliminate temporal information at high frequencies. Contrary to this belief, results of this analysis show that rate-place predictions for frequency discrimination are inconsistent with human performance in the dependence on frequency for high frequencies and that there is significant temporal information in the AN up to at least 10 kHz. In fact, the all-information predictions match the functional dependence of human performance on frequency, although optimal performance is much better than human performance. The use of computational AN models in this study provides new constraints on hypotheses of neural encoding of frequency in the auditory system; however, the method is limited to simple tasks with deterministic stimuli. A companion article in this issue (“Evaluating Auditory Performance Limits: II”) describes an extension of this approach to more complex tasks that include random variation of one parameter, for example, random-level variation, which is often used in psychophysics to test neural encoding hypotheses.