Dataset Information

Millisecond-scale motor encoding in a cortical vocal area.

ABSTRACT: Studies of motor control have almost universally examined firing rates to investigate how the brain shapes behavior. In principle, however, neurons could encode information through the precise temporal patterning of their spike trains as well as (or instead of) through their firing rates. Although the importance of spike timing has been demonstrated in sensory systems, it is largely unknown whether timing differences in motor areas could affect behavior. We tested the hypothesis that significant information about trial-by-trial variations in behavior is represented by spike timing in the songbird vocal motor system. We found that neurons in motor cortex convey information via spike timing far more often than via spike rate and that the amount of information conveyed at the millisecond timescale greatly exceeds the information available from spike counts. These results demonstrate that information can be represented by spike timing in motor circuits and suggest that timing variations evoke differences in behavior.

SUBMITTER: Tang C

PROVIDER: S-EPMC4260785 | biostudies-literature | 2014 Dec

REPOSITORIES: biostudies-literature

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Millisecond-scale motor encoding in a cortical vocal area.

Tang Claire C Chehayeb Diala D Srivastava Kyle K Nemenman Ilya I Sober Samuel J SJ

PLoS biology 20141209 12

Studies of motor control have almost universally examined firing rates to investigate how the brain shapes behavior. In principle, however, neurons could encode information through the precise temporal patterning of their spike trains as well as (or instead of) through their firing rates. Although the importance of spike timing has been demonstrated in sensory systems, it is largely unknown whether timing differences in motor areas could affect behavior. We tested the hypothesis that significant ...[more]

PMID: 25490022

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Project description:Segmenting objects from each other and their background is critical for vision. The speed at which objects move provides a salient cue for segmentation. However, how the visual system represents and differentiates multiple speeds is largely unknown. Here we investigated the neural encoding of multiple speeds of overlapping stimuli in the primate visual cortex. We first characterized the perceptual capacity of human and monkey subjects to segment spatially overlapping stimuli moving at different speeds. We then determined how neurons in the motion-sensitive, middle-temporal (MT) cortex of macaque monkeys encode multiple speeds. We made a novel finding that the responses of MT neurons to two speeds of overlapping stimuli showed a robust bias toward the faster speed component when both speeds were slow (≤ 20°/s). The faster-speed bias occurred even when a neuron had a slow preferred speed and responded more strongly to the slower component than the faster component when presented alone. The faster-speed bias emerged very early in neuronal response and was robust over time and to manipulations of motion direction and attention. As the stimulus speed increased, the faster-speed bias changed to response averaging. Our finding can be explained by a modified divisive normalization model, in which the weights for the speed components are proportional to the responses of a population of neurons elicited by the individual speeds. Our results suggest that the neuron population, referred to as the weighting pool, includes neurons that have a broad range of speed preferences. As a result, the response weights for the speed components are determined by the stimulus speeds and invariant to the speed preferences of individual neurons. Our findings help to define the neural encoding rule of multiple stimuli and provide new insight into the underlying neural mechanisms. The faster-speed bias would benefit behavioral tasks such as figure-ground segregation if figural objects tend to move faster than the background in the natural environment.

Dataset Information

Millisecond-scale motor encoding in a cortical vocal area.

Publications

Millisecond-scale motor encoding in a cortical vocal area.

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