Observers can detect interaural delays in three component stimuli produced by sinusoidally modulating the amplitude of a sinusoidal carrier. Interaural delays are detected in stimuli confined to a high-frequency region even in the presence of an intense, low-pass filtered noise. With 300-Hz modulation of a 3900-Hz carrier, detection of interaural delay is equally good when either the entire stimulus or just the envelope of the stimulus is delayed. In either case performance is as good as with a 300-Hz pure tone.
Human listeners can localize sounds by the difference in both arrival time (phase) and loudness between the two ears. Movement of the sound source modulates these cues, and responses to moving sounds have been detected in animals in primary auditory cortex and in humans in other cortical areas. Here we show that detection of changes in the interaural phase or amplitude difference occurs through a mechanism distinct from that used to detect changes in one ear alone. Moreover, a patient with a right hemisphere stroke is unable to detect sound movement, regardless of whether it is defined by phase or by loudness cues. We propose that this deficit reflects damage to a distinct cortical area, outside the classical auditory areas, that is specialized for the detection of sound motion. The deficit is analagous to cerebral akinotopsia (motion blindness) in the visual system, and so the auditory system may, like the visual system, show localization of specialized functions to different cortical regions.
The detectability of a sinusoidal grating was measured in a standard two-interval forced-choice experiment against backgrounds of noise gratings of the same orientation as the signal. The noise gratings were either spatially high-pass or low-pass filtered and were either unchanged in each observation interval (static) or flickering at a rate that depended on their cutoff frequency (dynamic). Spatial-frequency-selective mechanisms are inferred from the data and their characteristics shown to depend on assumptions concerning the detection process thought to follow the spatial-frequency-selective device.
Flickering long-wavelength light appears more yellow than steady light of the same average intensity. The hue change is consistent with distortion of the visual signal at some nonlinear site (or sites) that produces temporal components not present in the original stimulus (known as distortion products). We extracted the temporal attenuation characteristics of the early (prenonlinearity) and late (post-nonlinearity) filter stages in the L- and M-cone chromatic pathway by varying the input stimulus to manipulate the distortion products and the measuring of the observers' sensitivity to them. The early, linear, filter stage acts like a band-pass filter peaking at 10-15 Hz with substantial sensitivity losses at both lower and higher frequencies. Its characteristics are consistent with nonlinearity being early in the visual pathway but following surround inhibition. The late stage, in contrast, acts like a low-pass filter with a cutoff frequency around 3 Hz. The response of the early stage speeds up with radiance, but the late stage does not. A plausible site for the nonlinearity, which modelling suggests may be smoothly compressive but with a hard limit at high input levels, is after surround inhibition from the horizontal cells.
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