Hand and finger postures of other people are important body language cues that strongly contribute to the observer's decision about the person's intentions, thoughts, and attentional state. We compared neuromagnetic cortical activation elicited by color images of natural and distorted finger postures. The distorted postures contained computer-deformed joint angles and thereby easily caught the observer's attention. From about 260 msec onwards, extrastriate occipital areas of both hemispheres were activated more strongly by distorted than natural finger postures. We interpret this result as an early topdown effect of emotional valence on the processing of unusual hand shapes in the extrastriate visual cortex.

Auditory cortical processing of speech-like sounds was studied in 9 dyslexic and 11 normal-reading adults. Noise/ square-wave sequences, mimicking transitions from a fricative consonant to a vowel, were presented binaurally once every 1.1 sec and the cortical responses were recorded with a whole-scalp neuromagnetometer. The auditory cortices of both hemispheres were less reactive to acoustical changes in dyslexics than in controls, as was evident from the weaker responses to the noise/square-wave transitions. The results demonstrate that dyslexic adults are deficient in processing acoustic changes presented in rapid succession within tens to hundreds of milliseconds. The observed differences could be related to insufficient triggering of automatic auditory attention, resulting, for instance, from a general deficiency of the magnocellular system.

The speed of visually triggered movements depends, among other things, on the time needed for visuomotor transformations. We show that it takes on average 20–40 msec less time to respond to visual stimuli when they are projected on the reacting fingers than a few centimeters away from them. The result implies significant preference of the personal space to the extrapersonal space for stimuli used in the initiation of visually triggered movements.

Neuromagnetic responses were recorded to frequent "standard tones of l000 Hz and to infrequent 1100-Hz "deviant" tones with a 24-channel planar SQUID gradiometer. Stimuli were presented at constant interstimulus intervals (ISIs) ranging from 0.75 to 12 sec. The standards evoked a prominent 100-msec response, N100m, which increased in amplitude with increasing ISI. N100m could be dissociated into two subcomponents with different source areas. The posterior component, N100m 2 , increased when the ISI grew up to 6 sec, whereas the more anterior component, N100m 2 , probably continued its growth beyond the 12-sec ISI. At ISIs from 0.75 to 9 sec, the deviants elicited additionally a mismatch field (MMF). The equivalent sources of both N100m and MMF were at the supra-temporal auditory cortex. We assume that auditory stimuli leave in the auditory system a trace that affects the processing of the subsequent stimuli. The decrement of the N100m amplitude as well as elicitation of MMF can be considered as indirect evidence of active traces. A behavioral estimate of the persistence of the sensory auditory memory was obtained in a separate experiment in which the subject compared, without attending to the stimuli, tones presented at the daerent ISIs. The subjects discriminated the stimuli better than merely by chance at ISIs of 0.75-9 sec. The ISI dependence of the behavioral estimate as well as of N100m 2 and MMF are similar enough to suggest a common underlying mechanism that retains information for a period of about 10 sec.