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A frequency analysis was used to tag cortical activity from imagined rhythmic movements. Participants synchronized overt and imagined taps with brief visual stimuli presented at a constant rate, alternating between left and right index fingers. Brain potentials were recorded from across the scalp and topographic maps made of their power at the alternation frequency between left and right taps. Two prominent power foci occurred in each hemisphere for both overt and imagined taps, one over sensorimotor cortex and the other over posterior parietal cortex, with homologous foci in opposite hemispheres arising from oscillations 180 [degree] out of phase. These findings demonstrate temporal isomorphism at a neural level between overt and imagined movements and illustrate a new approach to studying covert actions.

Lateralized readiness potentials (LRPs) were used to determine the stage(s) of reaction time (RT) responsible for speed-accuracy trade-offs (SATs). Speeded decisions based on several types of information were examined in 3 experiments, involving, respectively, a line discrimination task, lexical decisions, and an Erikson flanker task. Three levels of SAT were obtained in each experiment by adjusting response deadlines with an adaptive tracking algorithm. Speed stress affected the duration of RT stages both before and after the start of the LRP in all experiments. The latter effect cannot be explained by guessing strategies, by variations in response force, or as an indirect consequence of the pre-LRP effect. Contrary to most models, it suggests that SAT can occur at a late postdecisional stage.

A frequency analysis was used to tag cortical activity from imagined rhythmic movements. Participants synchronized overt and imagined taps with brief visual stimuli presented at a constant rate, alternating between left and right index fingers. Brain potentials were recorded from across the scalp and topographic maps made of their power at the alternation frequency between left and right taps. Two prominent power foci occurred in each hemisphere for both overt and imagined taps, one over sensorimotor cortex and the other over posterior parietal cortex, with homologous foci in opposite hemispheres arising from oscillations 180[degrees] out of phase. These findings demonstrate temporal isomorphism at a neural level between overt and imagined movements and illustrate a new approach to studying covert actions. Keywords: covert motor processes, motor imagery, synchronization tapping, movement-related brain potentials, frequency tagging

Lateralized readiness potentials (LRPs) were used to determine the stage(s) of reaction time (RT) responsible for speed--accuracy trade-offs (SATs). Speeded decisions based on several types of information were examined in 3 experiments, involving, respectively, a line discrimination task, lexical decisions, and an Erikson flanker task. Three levels of SAT were obtained in each experiment by adjusting response deadlines with an adaptive tracking algorithm. Speed stress affected the duration of RT stages both before and after the start of the LRP in all experiments. The latter effect cannot be explained by guessing strategies, by variations in response force, or as an indirect consequence of the pre-LRP effect. Contrary to most models, it suggests that SAT can occur at a late postdecisional stage.

We sought to measure separately the motor potentials for each of 2 concurrent tasks and to use these measurements to identify the locus of dual-task interference. Lateralized readiness potentials (LRPs) were measured in the psychological refractory period paradigm, in which a separate response is required to each of 2 successive signals. As the interval between the signals decreased, the 2 reaction time (RT) tasks increasingly overlapped and the 2nd RT was prolonged. The LRP for the 2nd task was also delayed but maintained a constant temporal relation with the 2nd RT and sometimes preceded the 1st-task RT. The results indicate that (a) independent measures of the LRP can be obtained for each of 2 concurrent tasks, (b) slowing of the 2nd task was caused by a delay in processes that precede LRP onset, and (c) the 1st task may cease to interfere with the 2nd considerably before producing an overt response.

The complexity of a movement is known to affect the time it takes to initiate the movement. This effect is thought to reflect changes in the duration of processes that operate on a motor program. This question addressed here is whether programming a movement compels the start of its overt execution. If it does, then the programming processes may be said to occur after the 'point of no return.' We report results from an empirical procedure and a theoretical analysis designed to study processes before and after this point separately. According to our results, changes in the complexity of a movement affect only the prior set of processes. From this we argue that motor programming does not necessitate response execution and that the point of no return occurs very late in the information-processing system.

A clock paradigm was employed to assess whether temporal preparation decreases the time to detect the onset of a stimulus - that is, perceptual latency. In four experiments participants watched a revolving clock hand while listening to soft or loud target tones under high or low temporal preparation. At the end of each trial, participants reported the clock hand position at the onset of the target tone. The deviation of the reported clock hand position from the actual position indexed perceptual latency. As expected, perceptual latency decreased with target tone intensity. Most importantly, however, greater temporal preparation decreased perceptual latency in all four experiments, especially for soft tones, which supports rather directly the idea that temporal preparation diminishes the duration of perceptual processing.

Though each foot is controlled primarily by the contralateral hemisphere, the event-related brain potentials preceding an overt foot movement are largest over the ipsilateral side of the head. Because such "paradoxical lateralization" results from the spatial organization of the motor homunculus, it can provide a sign of motor-cortex activation. We report paradoxical lateralization in the potentials accompanying imagined foot movements, thereby demonstrating a contribution of cortical areas directly involved in movement execution.