Literature DB >> 1486950

Head movement propensity.

J H Fuller1.   

Abstract

In studies of human eye-head coordinated saccadic gaze shifts, different laboratories have found greatly different magnitudes of head movements for a given amplitude of gaze shift (head movement gain). The present study was conducted to examine why, and to quantify volitional head movements. Fixation/target lights were located at 20 degrees and 40 degrees on either side of a central light. There were two tasks or modes. In the non-aligned mode, gaze fixation (first light) was followed by a gaze step to the target (second light) accurately and quickly. In the head-aligned mode, the head was aligned within 3 degrees of the first fixation light (i.e., initial starting position) before the step sequence began. In both non-aligned and head-aligned modes, subject instructions pertaining to the second target light concerned only gaze; there was no requisite head position. The head movement propensity of nine subjects was ranked according to the mean gain (head/target amplitude) of two 40 degree jumps (0-40 degrees and -20 to +20 degrees) in the non-aligned mode. This ranking method clearly identified extreme head-movers and non-movers. The moderate movers were further characterized by three additional criteria, derived by comparing the gains in different jumps, which varied in starting position and amplitude. First, when the two 40 degree jumps were compared, typically the gain of non-movers was less in the symmetric jump (-20 to +20 degrees) with the gain of the head-movers was greater in the symmetric jump. Second, in the head-aligned mode the gain of non-movers progressively increased when the starting position was progressively moved eccentrically, whereas the gain of head-movers increased only slightly, if at all. Third, when the gains of two symmetric (40 degrees and 80 degrees) jumps were compared, the head-movers consistently had opposite trends from non-movers. These three comparative criteria and the initial criterion together define head movement propensity. To explain the above observations, three effects are proposed. First, a "midline-attraction" effect causes resistance to movement away from the midline in non-movers and an increase in movement amplitude if the jump starts eccentrically. Second, a "resetting" effect occurs when the eccentricity of the jump is varied; the stopping position is reset closer to the target. Third, an "awareness/arousal" effect increases the gain in the head-aligned mode due to the intrinsic nature of the alignment procedure.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1992        PMID: 1486950     DOI: 10.1007/bf00230391

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  12 in total

1.  The primary position of the eyes, the resetting saccade, and the transverse visual head plane. Head movements around the cervical joints.

Authors:  R S Jampel; D X Shi
Journal:  Invest Ophthalmol Vis Sci       Date:  1992-07       Impact factor: 4.799

2.  A neural network model of sensoritopic maps with predictive short-term memory properties.

Authors:  J Droulez; A Berthoz
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-01       Impact factor: 11.205

Review 3.  The neurobiology of saccadic eye movements. Metrics.

Authors:  W Becker
Journal:  Rev Oculomot Res       Date:  1989

4.  Vestibulo-ocular function during co-ordinated head and eye movements to acquire visual targets.

Authors:  G R Barnes
Journal:  J Physiol       Date:  1979-02       Impact factor: 5.182

5.  A reexamination of the gain of the vestibuloocular reflex.

Authors:  E Viirre; D Tweed; K Milner; T Vilis
Journal:  J Neurophysiol       Date:  1986-08       Impact factor: 2.714

6.  Combined eye-head gaze shifts in the primate. I. Metrics.

Authors:  R D Tomlinson; P S Bahra
Journal:  J Neurophysiol       Date:  1986-12       Impact factor: 2.714

7.  Coordination of head and eye movements to fixate continuous and intermittent targets.

Authors:  M A Gresty
Journal:  Vision Res       Date:  1974-06       Impact factor: 1.886

8.  Active head rotations and eye-head coordination.

Authors:  W H Zangemeister; L Stark
Journal:  Ann N Y Acad Sci       Date:  1981       Impact factor: 5.691

9.  Eye and head movements during vestibular stimulation in the alert rabbit.

Authors:  J H Fuller
Journal:  Brain Res       Date:  1981-02-02       Impact factor: 3.252

10.  Gaze control in humans: eye-head coordination during orienting movements to targets within and beyond the oculomotor range.

Authors:  D Guitton; M Volle
Journal:  J Neurophysiol       Date:  1987-09       Impact factor: 2.714

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  33 in total

1.  The influence of future gaze orientation upon eye-head coupling during saccades.

Authors:  Brian S Oommen; Ryan M Smith; John S Stahl
Journal:  Exp Brain Res       Date:  2003-11-12       Impact factor: 1.972

2.  Head-eye interactions during vertical gaze shifts made by rhesus monkeys.

Authors:  Edward G Freedman
Journal:  Exp Brain Res       Date:  2005-08-13       Impact factor: 1.972

3.  Kinematics and eye-head coordination of gaze shifts evoked from different sites in the superior colliculus of the cat.

Authors:  Alain Guillaume; Denis Pélisson
Journal:  J Physiol       Date:  2006-10-05       Impact factor: 5.182

4.  Eye position modulates the electromyographic responses of neck muscles to electrical stimulation of the superior colliculus in the alert cat.

Authors:  K Hadjidimitrakis; A K Moschovakis; Y Dalezios; A Grantyn
Journal:  Exp Brain Res       Date:  2006-11-08       Impact factor: 1.972

5.  Anatomical evidence for interconnections between the central mesencephalic reticular formation and cervical spinal cord in the cat and macaque.

Authors:  Susan Warren; David M Waitzman; Paul J May
Journal:  Anat Rec (Hoboken)       Date:  2008-02       Impact factor: 2.064

6.  Eye-head coupling tendencies in stationary and moving subjects.

Authors:  Zachary C Thumser; John S Stahl
Journal:  Exp Brain Res       Date:  2009-04-26       Impact factor: 1.972

7.  Idiosyncratic variations in eye-head coupling observed in the laboratory also manifest during spontaneous behavior in a natural setting.

Authors:  Zachary C Thumser; Brian S Oommen; Igor S Kofman; John S Stahl
Journal:  Exp Brain Res       Date:  2008-08-15       Impact factor: 1.972

8.  Guidance of visual direction by topographical vibrotactile cues on the torso.

Authors:  Francois Asseman; Adolfo M Bronstein; Michael A Gresty
Journal:  Exp Brain Res       Date:  2007-12-11       Impact factor: 1.972

9.  Gaze shifts to auditory and visual stimuli in cats.

Authors:  Janet L Ruhland; Tom C T Yin; Daniel J Tollin
Journal:  J Assoc Res Otolaryngol       Date:  2013-06-08

10.  Eye position and target amplitude effects on human visual saccadic latencies.

Authors:  J H Fuller
Journal:  Exp Brain Res       Date:  1996-06       Impact factor: 1.972

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