Skip to main content
Log in

Error generalization as a function of velocity and duration: human reaching movements

  • Research Article
  • Published:
Experimental Brain Research Aims and scope Submit manuscript

Abstract

Our sensory-motor control system has a remarkable ability to adapt to novel dynamics during reaching movements and generalizes this adaptation to movements made in different directions, positions and even speeds. The degree and pattern of this generalization are of great importance in deducing the underlying mechanisms that govern our motor control. In this report we expand our knowledge on the generalization between movements made at different speeds. We wished to determine the pattern of generalization between different speed and duration movements on a trial-by-trial basis. In addition, we tested three hypotheses for the pattern of generalization. The first hypothesis was that the generalization was maximum for the speed of the movement just made with a linear decrease in generalization as one moves away from that preferred speed. The second was that the generalization is always highest for the fastest speed movements and linearly decreases with speed. The last hypothesis came from our preliminary results, which suggested that the generalization plateaus. Human subjects made targeted reaching movements at four different maximum speeds (15, 35, 55 and 75 cm/s) presented in pseudorandom order to one spatial target (15 cm extent) while holding onto a robotic manipulandum that produced a viscous curl field. Catch trials (trial where the curl field was unexpectedly removed) were used to probe the generalization between the four speed/durations on a movement-by-movement basis. We found that the pattern of generalization was linear between the first three speed categories (15–55 cm/s), but plateaued after the 55 cm/s category. We compared the subjects’ results with a simulated adaptive controller that used a population code by combining the output of basis elements. These basis elements encoded limb velocity and associated this with a force expectation at that velocity. We found that using a basis set of Gaussians the adaptive controller produced movements that generalized in virtually the exact manner as the subjects, as we have previously demonstrated for movements made to different spatial targets. Thus, the human internal model may employ such a population code.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8

Similar content being viewed by others

References

  • Bock O, Thomas M, Grigorova V (2005) The effect of rest breaks on human sensorimotor adaptation. Exp Brain Res 163:258–260

    Article  PubMed  Google Scholar 

  • Churchland MM, Santhanam G, Shenoy KV (2006) Preparatory activity in premotor and motor cortex reflects the speed of the upcoming reach. J Neurophysiol 96:3130–3146

    Article  PubMed  Google Scholar 

  • Donchin O, Shadmehr R (2004) Change of desired trajectory caused by training in a novel motor task. Conf Proc IEEE Eng Med Biol Soc 6: 4495–4498

    PubMed  CAS  Google Scholar 

  • Donchin O, Francis JT, Shadmehr R (2003) Quantifying generalization from trial-by-trial behavior of adaptive systems that learn with basis functions: theory and experiments in human motor control. J Neurosci 23: 9032–9045

    PubMed  CAS  Google Scholar 

  • Evarts EV (1968) Relation of pyramidal tract activity to force exerted during voluntary movement. J Neurophysiol 31:14–27

    PubMed  CAS  Google Scholar 

  • Flash T, Hogan N (1985) The coordination of arm movements: an experimentally confirmed mathematical model. J Neurosci 5:1688–1703

    PubMed  CAS  Google Scholar 

  • Francis JT (2005) Influence of the inter-reach-interval on motor learning. Exp Brain Res 167:128–131

    Article  PubMed  Google Scholar 

  • Franklin DW, Osu R, Burdet E, Kawato M, Milner TE (2003) Adaptation to stable and unstable dynamics achieved by combined impedance control and inverse dynamics model. J Neurophysiol 90:3270–3282

    Article  PubMed  Google Scholar 

  • Fu QG, Suarez JI, Ebner TJ (1993) Neuronal specification of direction and distance during reaching movements in the superior precentral premotor area and primary motor cortex of monkeys. J Neurophysiol 70: 2097–2116

    PubMed  CAS  Google Scholar 

  • Gandolfo F, Mussa-Ivaldi FA, Bizzi E (1996) Motor learning by field approximation. Proc Natl Acad Sci USA 93:3843–3846

    Article  PubMed  CAS  Google Scholar 

  • Georgopoulos AP, Kalaska JF, Caminiti R, Massey JT (1982) On the relations between the direction of two-dimensional arm movements and cell discharge in primate motor cortex. J Neurosci 2:1527–1537

    PubMed  CAS  Google Scholar 

  • Georgopoulos AP, Kettner RE, Schwartz AB (1988) Primate motor cortex and free arm movements to visual targets in three-dimensional space. II. Coding of the direction of movement by a neuronal population. J Neurosci 8:2928–2937

    PubMed  CAS  Google Scholar 

  • Goodbody SJ, Wolpert DM (1998) Temporal and amplitude generalization in motor learning. J Neurophysiol 79:1825–1838

    PubMed  CAS  Google Scholar 

  • Gribble PL, Mullin LI, Cothros N, Mattar A (2003) Role of cocontraction in arm movement accuracy. J Neurophysiol 89:2396–2405

    Article  PubMed  Google Scholar 

  • Harris CM, Wolpert DM (1998) Signal-dependent noise determines motor planning. Nature 394:780–784

    Article  PubMed  CAS  Google Scholar 

  • Huang VS, Shadmehr R (2007) Evolution of motor memory during the seconds after observation of motor error. J Neurophysiol 97:3976–3985

    Article  PubMed  Google Scholar 

  • Kitazawa S, Kimura T, Uka T (1997) Prism adaptation of reaching movements: specificity for the velocity of reaching. J Neurosci 17: 1481–1492

    PubMed  CAS  Google Scholar 

  • Kording KP, Fukunaga I, Howard IS, Ingram JN, Wolpert DM (2004) A neuroeconomics approach to inferring utility functions in sensorimotor control. PLoS Biol 2:e330

    Article  PubMed  Google Scholar 

  • Krouchev NI, Kalaska JF (2003) Context-dependent anticipation of different task dynamics: rapid recall of appropriate motor skills using visual cues. J Neurophysiol 89:1165–1175

    Article  PubMed  Google Scholar 

  • Lackner JR, Dizio P (1994) Rapid adaptation to Coriolis force perturbations of arm trajectory. J Neurophysiol 72:299–313

    PubMed  CAS  Google Scholar 

  • Moran DW, Schwartz AB (1999) Motor cortical representation of speed and direction during reaching. J Neurophysiol 82:2676–2692

    PubMed  CAS  Google Scholar 

  • Nakano E, Imamizu H, Osu R, Uno Y, Gomi H, Yoshioka T, Kawato M (1999) Quantitative examinations of internal representations for arm trajectory planning: minimum commanded torque change model. J Neurophysiol 81: 2140–2155

    PubMed  CAS  Google Scholar 

  • Osu R, Kamimura N, Iwasaki H, Nakano E, Harris CM, Wada Y, Kawato M (2004) Optimal impedance control for task achievement in the presence of signal-dependent noise. J Neurophysiol 92:1199–1215

    Article  PubMed  Google Scholar 

  • Pouget A, Snyder LH (2000) Computational approaches to sensorimotor transformations. Nat Neurosci 3(Suppl):1192–1198

    Article  PubMed  CAS  Google Scholar 

  • Scheidt RA, Dingwell JB, Mussa-Ivaldi FA (2001) Learning to move amid uncertainty. J Neurophysiol 86:971–985

    PubMed  CAS  Google Scholar 

  • Shadmehr R, Mussa-Ivaldi FA (1994) Adaptive representation of dynamics during learning of a motor task. J Neurosci 14:3208–3224

    PubMed  CAS  Google Scholar 

  • Shadmehr R, Donchin O, Hwang EJ, Hemminger SE, Rao A (2005) Learning dynamics of reaching. CRC, Boca Raton

    Google Scholar 

  • Thoroughman KA, Shadmehr R (2000) Learning of action through adaptive combination of motor primitives [see comments]. Nature 407:742–747

    Article  PubMed  CAS  Google Scholar 

  • Uno Y, Kawato M, Suzuki R (1989) Formation and control of optimal trajectory in human multijoint arm movement. Minimum torque-change model. Biol Cybern 61:89–101

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

I would like to thank Reza Shadmehr for the use of his manipulandum as well as helpful conversation and Sarah Hemminger for proofreading of the manuscript. This work was supported by NIH 2-R01-NS037422 to RS.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Joseph T. Francis.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Francis, J.T. Error generalization as a function of velocity and duration: human reaching movements. Exp Brain Res 186, 23–37 (2008). https://doi.org/10.1007/s00221-007-1202-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00221-007-1202-y

Keywords

Navigation