1. Responses of neurons in the auditory cortex of the albino rat were examined using microelectrode mapping techniques. Characteristic frequencies were determined for numerous electrode penetrations across the cortical surface in individual animals. A primary auditory area was identified in the posterolateral neocortex that was characterized by short latency responses to tone bursts and tonotopic organization with high frequencies represented rostrally and low frequencies, caudally. Within this area cells with similar characteristic frequencies were aligned in a dorsoventral orientation to form isofrequency contours. 2. Tuning curves obtained from primary auditory cortex were characteristically "V" shaped with Q10's ranging from 0.97 to 28.4. Maximum Q10 values increased monotonically with characteristic frequency (CF). The lowest thresholds at CF closely approximated the behavioral audiogram for the albino rat. Many neurons, however, had CF thresholds well above the behavioral limit. 3. Areas were found dorsal and ventral to the primary auditory cortex in which CF's were clearly discontinuous with the neighboring isofrequency contours. These data suggest the presence of other auditory fields, the detailed characteristics of which have yet to be examined.

No abstract

To assess the role of second-order channels in symmetry perception we measured the effects of check size, spatial frequency content, eccentricity and grey scale range on the detection of symmetrical and anti-symmetrical patterns. Thresholds for symmetrical stimuli were only moderately affected by these manipulations. Anti-symmetrical stimuli composed of large black and white checks elicited low thresholds. However, anti-symmetry became essentially undetectable at small check sizes. Removing low frequencies from large-check-size, anti-symmetrical stimuli had little effect on thresholds whereas removing high frequencies had a pronounced effect. Moving the stimuli from fixation to 8 degrees eccentricity caused a dramatic increase in thresholds for anti-symmetrical stimuli but not symmetrical stimuli. When the grey scale range was increased anti-symmetry was undetectable at any check size whereas symmetry was easily seen at all. We argue that these results and others in the literature suggest that anti-symmetry is only detected under conditions favourable to selective attention.

1. The binaural response properties of neurons in the auditory cortex of the albino rat were examined using microelectrode mapping techniques. Characteristic frequencies, binaural response classes, and interaural intensity differences for binaural interaction were determined for multiple electrode penetrations across the cortical surface. The location of electrode penetrations was determined by reference to the cortical vascular pattern in individual animals. 2. When examined over a wide range of interaural intensities binaural responses could be classified as one of the following types: summation, i.e., excited by stimulation of either ear alone and facilitated by stimulation of both ears together (35.3%); suppression, i.e., excited by contralateral stimulation, unaffected by ipsilateral stimulation alone, but inhibited under binaural stimulus conditions (42.2%); mixed, i.e., facilitated by binaural stimulation at near threshold levels, but strongly inhibited by increased sound pressure levels in the ipsilateral ear (18.5%); or other, i.e., responses that could not be classified as any other type (4%). 3. Neurons of the summation and suppression class often exhibited binaural interaction when the intensities at both ears were approximately equal. The modal interaural intensity difference for both response types was between 0 and +5 dB. Neurons of the mixed interaction class were facilitate at near equal dichotic intensity but suppressed when the intensity in the ipsilateral ear was increased. The modal value was between 0 and +5 dB for summation and +20 dB for suppression. 4. Summation, suppression, and mixed binaural response types were found over a wide range of sound frequencies from 1 to 40 kHz. There was some tendency for summation responses to prevail at lower frequencies and suppression responses to prevail at higher frequencies but the differences were not large. Generally, responses from each of the three binaural classes were well represented over the rat's hearing range. 5. Cells of the same binaural response type were grouped together to form aggregates of summation, suppression, or mixed interaction patterns. Cortical areas with similar binaural response properties appeared in some cases to extend across isofrequency contours.

The study of cross-modal influences in perception, particularly between the auditory and visual modalities, has been intensified recently. This paper reports on a comprehensive study of auditory-visual cross-modal influences in motion, including motion aftereffects (MAE). We examined both auditory influences on visual perception and vice versa. Visual motion interactions were examined using three directional pairings or configurations: along the horizontal, vertical, and depth axes. In Experiment 1 we assessed how the simultaneous presence of a strong motion signal in one modality affected the perception of motion in the other modality. To investigate further whether such influences have long-term effects, we tested whether adaptation in one modality alone could produce cross-modal MAEs in Experiment 2. Overall, the pattern of results was similar across all directional pairings, with the strongest cross-modal influences observed in motion along the horizontal axis; this is likely due to the greater co-localization of the two stimuli in this configuration. Although both auditory and visual stimuli affected the other modality when presented simultaneously, significant cross-modally induced aftereffects could only be produced using visual stimuli. However, we did observe vertical visual MAE following adaptation to auditory spectral motion. These results are discussed in terms of current psychophysical and neurophysiological findings concerning the way in which auditory-visual signals are processed.