Abstract
Saccades exhibit variation in performance from one trial to the next, even when paced at a constant rate by targets at two fixed locations. We previously showed that amplitude fluctuations in consecutive predictive saccades have fractal structure: the spectrum of the sequence of consecutive amplitudes has a power-law (f −α) form, indicative of inter-trial correlations that reflect the storage of prior performance information to guide the planning of subsequent movements. More gradual decay of these inter-trial correlations coincides with a larger magnitude of spectral slope α, and indicates stronger information storage over longer times. We have previously demonstrated that larger decay exponents (α) are associated with faster adaptation in a saccadic double-step task. Here, we extend this line of investigation to predictive saccade endpoints (i.e., movement errors). Subjects made predictive, paced saccades between two fixed targets along a horizontal or vertical axis. Endpoint fluctuations both along (on-axis) and orthogonal to (off-axis) the direction of target motion were examined for correlations and fractal structure. Endpoints in the direction of target motion had little or no correlation or power-law scaling, suggesting that successive movements were uncorrelated (white noise). In the orthogonal direction, however, the sequence of endpoints did exhibit inter-trial correlations and scaling. In contrast, in our previous work the scaling of saccade amplitudes is strong along the target direction. This may reflect the fact that while saccade amplitudes are neurally programmed, endpoints are not directly controlled but instead serve as a source of error feedback. Hence, the lack of correlations in on-axis endpoint errors suggests that maximum information has been extracted from previous movement errors to plan subsequent movement amplitudes. In contrast, correlations in the off-axis component indicate that useful information still remains in this error (residual) sequence, suggesting that saccades are less tightly controlled along the orthogonal direction.
Highlights
The saccadic system generates rapid eye movements that shift the fovea from one place to another in the visual scene (Leigh and Zee, 2006; Ramat et al, 2007)
We have previously found inter-trial correlations between the latencies (Shelhamer and Joiner, 2003) and amplitudes (Wong and Shelhamer, 2011) of consecutive predictive saccades, such that the series of consecutive latencies or amplitudes exhibits long memory across large numbers of saccades
In our own work (Wong and Shelhamer, 2014) we found that stronger inter-trial correlations in the amplitudes of consecutive predictive saccades are associated with more rapid adjustment to target manipulations in a separate adaptation task
Summary
The saccadic system generates rapid eye movements that shift the fovea from one place to another in the visual scene (Leigh and Zee, 2006; Ramat et al, 2007). Saccade accuracy is established by an efferent copy of the ongoing motor command (Robinson, 1975; Wolpert et al, 1995; Optican, 2005). This efferent copy is used to predict the sensory effects of the movement (Quaia et al, 2000), which are compared to the actual movement outcome. Information about movement errors is stored and processed to adjust future saccade plans as needed to maintain accuracy
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