Auditory edge detection: a neural model for physiological and psychoacoustical responses to amplitude transients.

Primary segmentation of visual scenes is based on spatiotemporal edges that are presumably detected by neurons throughout the visual system. In contrast, the way in which the auditory system decomposes complex auditory scenes is substantially less clear. There is diverse physiological and psychophysical evidence for the sensitivity of the auditory system to amplitude transients, which can be considered as a partial analogue to visual spatiotemporal edges. However, there is currently no theoretical framework in which these phenomena can be associated or related to the perceptual task of auditory source segregation. We propose a neural model for an auditory temporal edge detector, whose underlying principles are similar to classical visual edge detector models. Our main result is that this model reproduces published physiological responses to amplitude transients collected at multiple levels of the auditory pathways using a variety of experimental procedures. Moreover, the model successfully predicts physiological responses to a new set of amplitude transients, collected in cat primary auditory cortex and medial geniculate body. Additionally, the model reproduces several published psychoacoustical responses to amplitude transients as well as the psychoacoustical data for amplitude edge detection reported here for the first time. These results support the hypothesis that the response of auditory neurons to amplitude transients is the correlate of psychoacoustical edge detection.

[1]  N. Suga,et al.  The inferior colliculus of the mustached bat has the frequency-vs-latency coordinates , 1997, Journal of Comparative Physiology A.

[2]  D. Irvine,et al.  First-spike timing of auditory-nerve fibers and comparison with auditory cortex. , 1997, Journal of neurophysiology.

[3]  R. Meddis,et al.  A computer model of amplitude-modulation sensitivity of single units in the inferior colliculus. , 1994, The Journal of the Acoustical Society of America.

[4]  Jos J. Eggermont,et al.  Differential effects of age on click-rate and amplitude modulation-frequency coding in primary auditory cortex of the cat , 1993, Hearing Research.

[5]  I Segev,et al.  Signal delay and input synchronization in passive dendritic structures. , 1993, Journal of neurophysiology.

[6]  M. M. Gibson,et al.  Initial discharge latency and threshold considerations for some neurons in cochlear nuclear complex of the cat. , 1978, Journal of neurophysiology.

[7]  Peter Heil,et al.  Topographic representation of tone intensity along the isofrequency axis of cat primary auditory cortex , 1994, Hearing Research.

[8]  E M Relkin,et al.  Psychophysical and physiological forward masking studies: probe duration and rise-time effects. , 1994, The Journal of the Acoustical Society of America.

[9]  D. P. Phillips,et al.  Factors shaping the response latencies of neurons in the cat's auditory cortex , 1998, Behavioural Brain Research.

[10]  D. Irvine,et al.  Functional specialization in auditory cortex: responses to frequency-modulated stimuli in the cat's posterior auditory field. , 1998, Journal of neurophysiology.

[11]  A S Bregman,et al.  Resetting the pitch-analysis system. 2. Role of sudden onsets and offsets in the perception of individual components in a cluster of overlapping tones. , 1994, The Journal of the Acoustical Society of America.

[12]  D P Phillips,et al.  Factors shaping the tone level sensitivity of single neurons in posterior field of cat auditory cortex. , 1995, Journal of neurophysiology.

[13]  M. Sachs,et al.  Rate versus level functions for auditory-nerve fibers in cats: tone-burst stimuli. , 1974, The Journal of the Acoustical Society of America.

[14]  D P Phillips,et al.  Effect of tone-pulse rise time on rate-level functions of cat auditory cortex neurons: excitatory and inhibitory processes shaping responses to tone onset. , 1988, Journal of neurophysiology.

[15]  Israel Nelken,et al.  Responses of auditory-cortex neurons to structural features of natural sounds , 1999, Nature.

[16]  M. L. Sutter,et al.  Functional topography of cat primary auditory cortex: response latencies , 1997, Journal of Comparative Physiology A.

[17]  C E Schreiner,et al.  Topography of intensity tuning in cat primary auditory cortex: single-neuron versus multiple-neuron recordings. , 1995, Journal of neurophysiology.

[18]  D P Phillips,et al.  Response magnitude and timing of auditory response initiation in the inferior colliculus of the awake chinchilla. , 1999, The Journal of the Acoustical Society of America.

[19]  R. Plomp,et al.  Effect of reducing slow temporal modulations on speech reception. , 1994, The Journal of the Acoustical Society of America.

[20]  A S Bregman,et al.  Resetting the pitch-analysis system: 1. Effects of rise times of tones in noise backgrounds or of harmonics in a complex tone , 1994, Perception & psychophysics.

[21]  P. Heil,et al.  Auditory cortical onset responses revisited. II. Response strength. , 1997, Journal of neurophysiology.

[22]  R Drullman,et al.  Temporal envelope and fine structure cues for speech intelligibility. , 1994, The Journal of the Acoustical Society of America.

[23]  Gerald Langner,et al.  Coding of temporal patterns in the central auditory nervous system , 1988 .

[24]  H. Barlow Vision: A computational investigation into the human representation and processing of visual information: David Marr. San Francisco: W. H. Freeman, 1982. pp. xvi + 397 , 1983 .

[25]  R. Meddis,et al.  Implementation details of a computation model of the inner hair‐cell auditory‐nerve synapse , 1990 .

[26]  C. Schreiner,et al.  Periodicity coding in the inferior colliculus of the cat. II. Topographical organization. , 1988, Journal of neurophysiology.

[27]  Peter Heil,et al.  Further observations on the threshold model of latency for auditory neurons , 1998, Behavioural Brain Research.

[28]  R. W. Rodieck Quantitative analysis of cat retinal ganglion cell response to visual stimuli. , 1965, Vision research.

[29]  N Suga,et al.  Responses of inferior collicular neurones of bats to tone bursts with different rise times , 1971, The Journal of physiology.

[30]  D. McCormick,et al.  Comparative electrophysiology of pyramidal and sparsely spiny stellate neurons of the neocortex. , 1985, Journal of neurophysiology.

[31]  Adrian Rees,et al.  Responses of neurons in the inferior colliculus of the rat to AM and FM tones , 1983, Hearing Research.

[32]  R. Burkard,et al.  Effects of noise burst rise time and level on the human brainstem auditory evoked response. , 1993, Audiology : official organ of the International Society of Audiology.

[33]  R V Shannon,et al.  Speech Recognition with Primarily Temporal Cues , 1995, Science.

[34]  David Marr,et al.  VISION A Computational Investigation into the Human Representation and Processing of Visual Information , 2009 .

[35]  P. Heil,et al.  Auditory cortical onset responses revisited. I. First-spike timing. , 1997, Journal of neurophysiology.

[36]  A. King,et al.  Auditory function: Neurobiological bases of hearing G.M. Edelman W.E. , 1990, Neuroscience.

[37]  H. Davis,et al.  Effects of duration and rise time of tone bursts on evoked V potentials. , 1968, The Journal of the Acoustical Society of America.

[38]  R. Plomp,et al.  Effect of temporal envelope smearing on speech reception. , 1994, The Journal of the Acoustical Society of America.

[39]  D. Irvine,et al.  On determinants of first‐spike latency in auditory cortex , 1996, Neuroreport.

[40]  D. Irvine,et al.  The posterior field P of cat auditory cortex: coding of envelope transients. , 1998, Cerebral cortex.

[41]  C E Schreiner,et al.  Functional topography of cat primary auditory cortex: distribution of integrated excitation. , 1990, Journal of neurophysiology.

[42]  John F. Olsen Rate of rise sensitivity of medial geniculate neurons in the squirrel monkey , 1995 .

[43]  Wolfgang Maass,et al.  Spiking Neurons , 1998, NC.