The anterior auditory field (AAF) is a large auditory representation in the cerebral cortex of the cat rostral to the ‘primary’ auditory cortex (AI) on the middle and anterior ectosylvian gyri. Fine-grained microelectrode maps of unit best frequencies were made in AAF of 16 ketamine anesthetized cats. Among the results were the following. (1) Most units in AAF that were driven by tonal stimuli had tuning curves with a single, sharply definable minimum (the best frequency). Occasionally, units were found to have multiple tuning curve minima. (2) In penetrations normal to the cortical surface of AAF, isolated units had remarkably similar tuning curves througout the middle and deep cortical layers. (3) In most of AAF, a restricted sector of the cochlear partition is represented by a straight belt of cortex crossing the entire field. (4) There is a highly ordered representation of the cochlea within AAF. The cortical belt representing the most basal sector of the cochlea (highest best frequencies) is oriented dorsoventrally along the border with the high frequency region of AI. Proceeding rostrally for some distance with AAF, lower frequency cortical belts are parallel to one another and maintain a highly ordered representation of progressively more apical cochlear sectors. The orientation of the lowest frequency representation usually rotates following the ventral curvature of the anterior ectosylvian gyrus. (5) In the portion of the field caudal to the axis of rotation of the representation, best frequency (represented cochlear position) is a simple (and apparently relatively constant) function of distance from the mutual high frequency AI-AAF border. (6) There is a propootionately larger representation of the highest frequency octaves within AAF. (7) The results of penetrations down the banks of the suprasylvian sulcus indicate that there may be units of vertical organization within AAF similar to those in AI, and in somatosensory and visual cortical fields. (8) The boundaries of AAF as well as the frequency representation within it are highly variable when referenced to cortical surface landmarks. (9) The cytoarchitectonic boundaries of AAF approximately correspond with the physiologically defined boundaries. (10) There were no cells driven to discharge by tonal stimuli in the fields dorsal and ventral to AAF. Comparison of the properties of AAF and AI show that these two fields are remarkably similar in many important features including unit response properties under ketamine anesthesia, short latency to earliest unit discharge, organization in depth, units of vertical organization, size, spatial representation of frequency and proportionately greater representation of higher frequency octaves. They also share some common thalamocortical inputs. These similarities suggest that AAF is not a ‘secondary’ cortical field, but, rather, that AAF and AI are virtually mirror images of one another and are co-participants in the earliest and fundamental processing of acoustic information at the cortical level.
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