A model of the mechanism of residue pitch perception is revisited. It is evaluated in the context of some new empirical results, and it is proposed that the model is able to reconcile a number of differing approaches in the history of theories of pitch perception. The model consists of four sequential processing stages: peripheral frequency selectivity, within-channel half-wave rectification and low-pass filtering, within-channel periodicity extraction, and cross-channel aggregation of the output. The pitch percept is represented by the aggregated periodicity function. Using autocorrelation as the periodicity extraction method and the summary autocorrelation function (SACF) as the method for representing pitch information, it is shown that the model can simulate new experimental results that show how the quality of the pitch percept is influenced by the resolvability of the harmonic components of the stimulus complex. These include: (i) the pitch of harmonic stimuli whose components alternate in phase; (ii) the increased frequency difference limen of tones consisting of higher harmonics; and (iii) the influence of a mistuned harmonic on the pitch of the complex as a function of its harmonic number. To accommodate these paradigms, it was necessary to compare stimuli along the length of the SACF rather than relying upon the highest peak alone. These new results demonstrate that the model responds differently to complexes consisting of low and high harmonics. As a consequence, it is not necessary to postulate two separate mechanisms to explain different pitch percepts associated with resolved and unresolved harmonics.
A revised computational model of the inner-hair cell (IHC) and auditory-nerve (AN) complex is presented and evaluated. Building on previous models, the algorithm is intended as a component for use in more comprehensive models of the auditory periphery. It combines smaller components that aim to be faithful to physiology in so far as is practicable and known. Transduction between cochlear mechanical motion and IHC receptor potential (RP) is simulated using a modification of an existing biophysical IHC model. Changes in RP control the opening of calcium ion channels near the synapse, and local calcium levels determine the probability of the release of neurotransmitter. AN adaptation results from transmitter depletion. The exact timing of AN action potentials is determined by the quantal and stochastic release of neurotransmitter into the cleft. The model reproduces a wide range of animal RP and AN observations. When the input to the model is taken from a suitably nonlinear simulation of the motion of the cochlear partition, the new algorithm is able to simulate the rate-intensity functions of low-, medium-, and high-spontaneous rate AN fibers in response to stimulation both at best frequency and at other frequencies. The variation in fiber type arises in large part from the manipulation of a single parameter in the model: maximum calcium conductance. The model also reproduces quantitatively phase-locking characteristics, relative refractory effects, mean-to-variance ratio, and first- and second-order discharge history effects.
Computational algorithms that mimic the response of the basilar membrane must be capable of reproducing a range of complex features that are characteristic of the animal observations. These include complex input output functions that are nonlinear near the site's best frequency, but linear elsewhere. This nonlinearity is critical when using the output of the algorithm as the input to models of inner hair cell function and subsequent auditory-nerve models of low- and high-spontaneous rate fibers. We present an algorithm that uses two processing units operating in parallel: one linear and the other compressively nonlinear. The output from the algorithm is the sum of the outputs of the linear and nonlinear processing units. Input to the algorithm is stapes motion and output represents basilar membrane motion. The algorithm is evaluated against published chinchilla and guinea pig observations of basilar membrane and Reissner's membrane motion made using laser velocimetry. The algorithm simulates both quantitatively and qualitatively, differences in input/output functions among three different sites along the cochlear partition. It also simulates quantitatively and qualitatively a range of phenomena including isovelocity functions, phase response, two-tone suppression, impulse response, and distortion products. The algorithm is potentially suitable for development as a bank of filters, for use in more comprehensive models of the peripheral auditory system.
A computational model of nervous activity in the auditory nerve, cochlear nucleus, and inferior colliculus is presented and evaluated in terms of its ability to simulate psychophysically-measured pitch perception. The model has a similar architecture to previous autocorrelation models except that the mathematical operations of autocorrelation are replaced by the combined action of thousands of physiologically plausible neuronal components. The evaluation employs pitch stimuli including complex tones with a missing fundamental frequency, tones with alternating phase, inharmonic tones with equally spaced frequencies and iterated rippled noise. Particular attention is paid to differences in response to resolved and unresolved component harmonics. The results indicate that the model is able to simulate qualitatively the related pitch-perceptions. This physiological model is similar in many respects to autocorrelation models of pitch and the success of the evaluations suggests that autocorrelation models may, after all, be physiologically plausible.
The aim of this study is to produce a functional model of the auditory nerve (AN) response of the guinea-pig that reproduces a wide range of important responses to auditory stimulation. The model is intended for use as an input to larger scale models of auditory processing in the brain-stem. A dual-resonance nonlinear filter architecture is used to reproduce the mechanical tuning of the cochlea. Transduction to the activity on the AN is accomplished with a recently proposed model of the inner-hair-cell. Together, these models have been shown to be able to reproduce the response of high-, medium-, and low-spontaneous rate fibers from the guinea-pig AN at high best frequencies (BFs). In this study we generate parameters that allow us to fit the AN model to data from a wide range of BFs. By varying the characteristics of the mechanical filtering as a function of the BF it was possible to reproduce the BF dependence of frequency-threshold tuning curves, AN rate-intensity functions at and away from BF, compression of the basilar membrane at BF as inferred from AN responses, and AN iso-intensity functions. The model is a convenient computational tool for the simulation of the range of nonlinear tuning and rate-responses found across the length of the guinea-pig cochlear nerve.
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