JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 87: 295-304, 2002;
0022-3077/02 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (13)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Medendorp, W. P.
Right arrow Articles by Gielen, C.C.A.M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Medendorp, W. P.
Right arrow Articles by Gielen, C.C.A.M.

The Journal of Neurophysiology Vol. 87 No. 1 January 2002, pp. 295-304
Copyright ©2002 by the American Physiological Society

Human Gaze Stabilization During Active Head Translations

W. P. Medendorp, J.A.M. Van Gisbergen, and C.C.A.M. Gielen

Department of Medical Physics and Biophysics, University of Nijmegen, NL 6525 EZ Nijmegen, The Netherlands

Medendorp, W. P., J.A.M. Van Gisbergen, and C.C.A.M. Gielen. Human Gaze Stabilization During Active Head Translations. J. Neurophysiol. 87: 295-304, 2002. This study investigated how binocular gaze is controlled to compensate for self-generated translational movements of the head where geometric requirements dictate that the ideal gaze signal needs to be modulated by the inverse of target distance. Binocular gaze (eye plus head) was measured for visual and remembered targets at various distances in six human subjects during active head translations at frequencies of 0.25, 0.5, 1.0, and 1.5 Hz. We found that, during head translations, gaze changes were achieved by a combination of eye and head rotations. Accordingly, stabilization performance was characterized by the gaze response parameters sensitivity and phase, where sensitivity is defined as the ratio of gaze velocity and translational eye velocity and where phase refers to the phase delay of gaze velocity relative to translational eye velocity. In the analysis, we used a binocular coordinate system yielding a version and a vergence component. We examined how frequency and target distance, estimated from the vergence angle, affected sensitivity and phase of the version component of the gaze signal and compared the results to the requirements for ideal performance. The relation between gaze sensitivity and the inverse of distance was characterized by a linear regression analysis. The ratio of the slope of the linear regression and the slope required for ideal stabilization provided a measure for the degree of "distance compensation." The results show that distance compensation was better for a visual target than for remembered targets in darkness, and behaved according to low-pass characteristics in both target conditions. It declined from 1.00 to 0.84 for visual targets and from 0.87 to 0.57 for remembered targets in the frequency range 0.25-1.5 Hz. The intercept obtained from the regression yielded the gaze response at zero vergence and specified a "default sensitivity" of gaze compensation. Default sensitivity increased with frequency from 0.02 at 0.25 Hz to 0.10°/cm at 1.5 Hz for visual targets and from 0.04 to 0.16°/cm in darkness. The phase delays of the gaze response increased on average from 2 to 7° in the frequency range 0.25-1.5 Hz. In comparison with earlier passive studies, active translation compensation in the dark is superior at all frequencies where comparison was possible. We conclude that a nonvestibular signal with low-pass characteristics contributes to gaze during active head translations.




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
R.A.A. Vingerhoets, W. P. Medendorp, and J.A.M. Van Gisbergen
Time Course and Magnitude of Illusory Translation Perception During Off-Vertical Axis Rotation
J Neurophysiol, March 1, 2006; 95(3): 1571 - 1587.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. A. Admiraal, N.L.W. Keijsers, and C.C.A.M. Gielen
Gaze Affects Pointing Toward Remembered Visual Targets After a Self-Initiated Step
J Neurophysiol, October 1, 2004; 92(4): 2380 - 2393.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. E. Angelaki
Eyes on Target: What Neurons Must do for the Vestibuloocular Reflex During Linear Motion
J Neurophysiol, July 1, 2004; 92(1): 20 - 35.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. Wei and D. E. Angelaki
Does Head Rotation Contribute to Gaze Stability During Passive Translations?
J Neurophysiol, April 1, 2004; 91(4): 1913 - 1918.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. A. Admiraal, N.L.W. Keijsers, and C.C.A.M. Gielen
Interaction Between Gaze and Pointing Toward Remembered Visual Targets
J Neurophysiol, October 1, 2003; 90(4): 2136 - 2148.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. Wei, G. C. DeAngelis, and D. E. Angelaki
Do Visual Cues Contribute to the Neural Estimate of Viewing Distance Used by the Oculomotor System?
J. Neurosci., September 10, 2003; 23(23): 8340 - 8350.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
W. P. Medendorp, D. B. Tweed, and J. D. Crawford
Motion Parallax Is Computed in the Updating of Human Spatial Memory
J. Neurosci., September 3, 2003; 23(22): 8135 - 8142.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online