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The influence of electrical stimulation of the superior colliculus (SC) on acoustically evoked responses of inferior collicular (IC) neurons was examined in 24 barbiturate-anesthetized Rufous horseshoe bats, Rhinolophus rouxi. Acoustic stimuli (50 ms, 0.5 ms rise-decay times) were delivered from a loudspeaker placed 68 cm in front of each bat and a total of 354 IC neurons were isolated. The response latencies of these neurons were mainly between 7.5 and 17.5 ms. When the ipsilateral SC was electrically stimulated, responses of 227 (64%) neurons were not affected, but responses of the remaining (127 neurons, 36%) were either inhibited (102 neurons, 29%) or facilitated (25 neurons, 7%). The degree of inhibition and the response latency of the inhibited neurons increased with the amplitude of electrical stimulation. Inhibition of a neuron's activity was also dependent upon the time interval between acoustic and electrical stimuli. The best inhibitory latency measured at maximal inhibition was between 12 and 20 ms. Conversely, facilitation shortened the response latency of IC neurons and the degree of facilitation increased with the amplitude of the acoustic stimulus. Since the SC plays an essential role in orienting an animal's responses toward sensory stimuli, our findings suggest that the SC may affect the processing of acoustic signals in the auditory system during acoustically guided orientation.

1. Frequency and space representation in the auditory cortex of the big brown bat, Eptesicus fuscus, were studied by recording responses of 223 neurons to acoustic stimuli presented in the bat's frontal auditory space. 2. The majority of the auditory cortical neurons were recorded at a depth of less than 500 microns with a response latency between 8 and 20 ms. They generally discharged phasically and had nonmonotonic intensity-rate functions. The minimum threshold, (MT) of these neurons was between 8 and 82 dB sound pressure level (SPL). Half of the cortical neurons showed spontaneous activity. All 55 threshold curves are V-shaped and can be described as broad, intermediate, or narrow. 3. Auditory cortical neurons are tonotopically organized along the anteroposterior axis of the auditory cortex. High-frequency-sensitive neurons are located anteriorly and low-frequency-sensitive neurons posteriorly. An overwhelming majority of neurons were sensitive to a frequency range between 30 and 75 kHz. 4. When a sound was delivered from the response center of a neuron on the bat's frontal auditory space, the neuron had its lowest MT. When the stimulus amplitude was increased above the MT, the neuron responded to sound delivered within a defined spatial area. The response center was not always at the geometric center of the spatial response area. The latter also expanded with stimulus amplitude. High-frequency-sensitive neurons tended to have smaller spatial response areas than low-frequency-sensitive neurons. 5. Response centers of all 223 neurons were located between 0 degrees and 50 degrees in azimuth, 2 degrees up and 25 degrees down in elevation of the contralateral frontal auditory space. Response centers of auditory cortical neurons tended to move toward the midline and slightly downward with increasing best frequency. 6. Auditory space representation appears to be systematically arranged according to the tonotopic axis of the auditory cortex. Thus, the lateral space is represented posteriorly and the middle space anteriorly. Space representation, however, is less systematic in the vertical direction. 7. Auditory cortical neurons are columnarly organized. Thus, the BFs, MTs, threshold curves, azimuthal location of response centers, and auditory spatial response areas of neurons sequentially isolated from an orthogonal electrode penetration are similar.

Corticofugal influences on the responses of inferior collicular neurons (IC) to acoustic stimulation were studied by electrical stimulation of the auditory cortex. Among 471 IC neurons isolated, about 26% were affected by cortical stimulation. Responses of 103 (22%) IC neurons were inhibited and 17 (3.6%) were facilitated. The degree of inhibition was dependent upon the amplitude of both auditory and electrical stimuli. Corticofugal inhibition of the response of an IC neuron was likely due to an increase in the neuron's minimum threshold. Inhibitory latency varied with the interstimulus interval. The shortest inhibitory latency of most IC neurons was between 1 and 2 ms. The localization of the point of cortical stimulation was crucial in determining the responses of IC neurons. It is assumed that corticofugal influences on IC neurons are a part of regulatory mechanism in the centrifugal pathway for frequency analysis and acoustic orientation.

Using free-field acoustic stimulus conditions, we studied the auditory space representation in the inferior colliculus (IC) of the big brown bat, Eptesicus fuscus, under different pinna positions. Stimuli were delivered from a loudspeaker placed 14 cm in front of the bat to determine the best frequency (BF) of an isolated neuron. A BF stimulus was then delivered as the loudspeaker was moved across the frontal auditory space of the bat to locate the response center of the neuron. At the response center, the neuron has its lowest minimum threshold (MT). The stimulus was then raised 5-dB above the lowest MT to measure the spatial response area. Both response center and spatial response area of each neuron were measured under different pinna positions. Variations in the response center and MT of each neuron under different pinna positions was determined and a possible reason for this variation was discussed. The variation in auditory space representation in the IC due to variation in pinna position is presented. We suggest that during echolocation a bat could make changes in its pinna position to create additional binaural disparity for accurate target localization.