Life or death in hostile environments depends crucially on one's ability to detect and gate novel sounds to awareness, such as that of a twig cracking under the paw of a stalking predator in a noisy jungle. Two distinct auditory cortex processes have been thought to underlie this phenomenon: (i) attenuation of the so-called N1 response with repeated stimulation and (ii) elicitation of a mismatch negativity response (MMN) by changes in repetitive aspects of auditory stimulation. This division has been based on previous studies suggesting that, unlike for the N1, repetitive ''standard'' stimuli preceding a physically different ''novel'' stimulus constitute a prerequisite to MMN elicitation, and that the source loci of MMN and N1 are different. Contradicting these findings, our combined electromagnetic, hemodynamic, and psychophysical data indicate that the MMN is generated as a result of differential adaptation of anterior and posterior auditory cortex N1 sources by preceding auditory stimulation. Early (Ϸ85 ms) neural activity within posterior auditory cortex is adapted as sound novelty decreases. This alters the center of gravity of electromagnetic N1 source activity, creating an illusory difference between N1 and MMN source loci when estimated by using equivalent current dipole fits. Further, our electroencephalography data show a robust MMN after a single standard event when the interval between two consecutive novel sounds is kept invariant. Our converging findings suggest that transient adaptation of feature-specific neurons within human posterior auditory cortex filters superfluous sounds from entering one's awareness.

Human neuroimaging studies suggest that localization and identification of relevant auditory objects are accomplished via parallel parietal-to-lateral-prefrontal ''where'' and anterior-temporal-toinferior-frontal ''what'' pathways, respectively. Using combined hemodynamic (functional MRI) and electromagnetic (magnetoencephalography) measurements, we investigated whether such dual pathways exist already in the human nonprimary auditory cortex, as suggested by animal models, and whether selective attention facilitates sound localization and identification by modulating these pathways in a feature-specific fashion. We found a double dissociation in response adaptation to sound pairs with phonetic vs. spatial sound changes, demonstrating that the human nonprimary auditory cortex indeed processes speech-sound identity

Considerable changes take place in the number of cerebral neurons, synapses and axons during development, mainly as a result of competition between different neural activities [1-4]. Studies using animals suggest that when input from one sensory modality is deprived early in development, the affected neural structures have the potential to mediate functions for the remaining modalities [5-8]. We now show that similar potential exists in the human auditory system: vibrotactile stimuli, applied on the palm and fingers of a congenitally deaf adult, activated his auditory cortices. The recorded magnetoencephalographic (MEG) signals also indicated that the auditory cortices were able to discriminate between the applied 180 Hz and 250 Hz vibration frequencies. Our findings suggest that human cortical areas, normally subserving hearing, may process vibrotactile information in the congenitally deaf.

Infrequent "deviant' auditory stimuli embedded in a homogeneous sequence of "standard' sounds evoke a neuromagnetic mismatch field (MMF), which is assumed to reflect automatic change detection in the brain. We investigated whether MMFs would reveal hemispheric differences in cortical auditory processing. Seven healthy adults were studied with a whole-scalp neuromagnetometer. The sound sequence, delivered to one ear at time, contained three infrequent deviants (differing from standards in duration, frequency, or interstimulus interval) intermixed with standard tones. MMFs peaked 9-34 msec earlier in the right than in the left hemisphere, irrespective of the stimulated ear. Whereas deviants activated only one MMF source in the left hemisphere, two temporally overlapping but spatially separate sources, one in the temporal lobe and another in the inferior parietal cortex, were necessary to explain the right-hemisphere MMFs. We suggest that the bilateral MMF components originating in the supratemporal cortex are feature specific whereas the right-hemisphere parietal component reflects more global auditory change detection. The results imply hemispheric differences in sound processing and suggest stronger involvement of the right than the left hemisphere in change detection.

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We investigated the temporal dependencies of N100 m, the most prominent deflection of the auditory evoked response, using whole-head neuromagnetic recordings. Stimuli were presented singly or in pairs (tones in the pair were separated by 210 ms) at interstimulus intervals (ISIs) of 0.6-8.1 s. N100 m to single stimuli and to the first tone of the pair had similar temporal recovery functions, plateauing at ISIs of 6 s. N100 m to the second tone in the pair, which was smaller than that to the first except with short ISIs, plateaued with ISIs of about 4 s. Source analysis revealed that the N100 m could be decomposed into two sources separated by about 1 cm on the supratemporal plane. The recovery function of the posterior source was not affected by stimulus presentation, whereas that of the anterior source was. Activity in the anterior area appears to reflect the effects of temporal integration. We relate these results to auditory sensory memory.

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