The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.
Gaze control in the cat: studies and modeling of the coupling between orienting eye and head movements in different behavioral tasks
Abstract
1. Orienting movements, consisting of coordinated eye and head displacements, direct the visual axis to the source of a sensory stimulus. A recent hypothesis suggests that the CNS may control gaze position (gaze = eye-relative-to-space = eye-relative-to-head + head-relative-to-space) by the use of a feedback circuit wherein an internally derived representation of gaze motor error drives both eye and head premotor circuits. In this paper we examine the effect of behavioral task on the individual and summed trajectories of horizontal eye- and head-orienting movements to gain more insight into how the eyes and head are coupled and controlled in different behavioral situations. 2. Cats whose heads were either restrained (head-fixed) or unrestrained (head-free) were trained to make orienting movements of any desired amplitude in a simple cat-and-mouse game we call the barrier paradigm. A rectangular opaque barrier was placed in front of the hungry animal who either oriented to a food target that was visible to one side of the barrier or oriented to a location on an edge of the barrier where it predicted the target would reappear from behind the barrier. 3. The dynamics (e.g., maximum velocity) and duration of eye- and head-orienting movements were affected by the task. Saccadic eye movements (head-fixed) elicited by the visible target attained greater velocity and had shorter durations than comparable amplitude saccades directed toward the predicted target. A similar observation has been made in human and monkey. In addition, when the head was unrestrained both the eye and head movements (and therefore gaze movements) were faster and shorter in the visible- compared with the predicted-target conditions. Nevertheless, the relative contributions of the eye and head to the overall gaze displacement remained task independent: i.e., the distance traveled by the eye and head movements was determined by the size of the gaze shift only. This relationship was maintained because the velocities of the eye and head movements covaried in the different behavioral situations. Gaze-velocity profiles also had characteristic shapes that were dependent on task. In the predicted-target condition these profiles tended to have flattened peaks, whereas when the target was visible the peaks were sharper. 4. Presentation of a visual cue (e.g., reappearance of food target) immediately before (less than 50 ms) the onset of a gaze shift to a predicted target triggered a midflight increase in first the eye- and, after approximately 20 ms, the head-movement velocity.(ABSTRACT TRUNCATED AT 400 WORDS)
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Primate frontal eye fields. I. Single neurons discharging before saccades
Bruce, C. J., & Goldberg, M. E. (1985) · Journal of Neurophysiology · doi:10.1152/jn.1985.53.3.603 · Cited by 1,394
Guitton, D., Buchtel, H. A., & Douglas, R. M. (1985) · Experimental Brain Research · doi:10.1007/bf00235863 · Cited by 1,005
Self-citationHikosaka, O., & Wurtz, R. H. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.5.1285 · Cited by 808
Human express saccades: extremely short reaction times of goal directed eye movements
Fischer, B., & Ramsperger, E. (1984) · Experimental Brain Research · doi:10.1007/bf00231145 · Cited by 701
Hikosaka, O., & Wurtz, R. H. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.5.1268 · Cited by 694
Hikosaka, O., & Wurtz, R. H. (1985) · Journal of Neurophysiology · doi:10.1152/jn.1985.53.1.266 · Cited by 689
Guitton, D., & Volle, M. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.58.3.427 · Cited by 627
Self-citationActivity of brain stem neurons during eye movements of alert monkeys.
Luschei, E. S., & Fuchs, A. F. (1972) · Journal of Neurophysiology · doi:10.1152/jn.1972.35.4.445 · Cited by 581
Brainstem Control of Saccadic Eye Movements
Fuchs, A. F., Kaneko, C. R. S., & Scudder, C. A. (1985) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.08.030185.001515 · Cited by 579
Hikosaka, O., Sakamoto, M., & Usui, S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.4.814 · Cited by 579
Cited by
Motor Functions of the Superior Colliculus
Gandhi, N. J., & Katnani, H. A. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113728 · Cited by 490
Does the nervous system depend on kinesthetic information to control natural limb movements?
Gandevia, S. C., & Burke, D. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0007254x · Cited by 359
The representation of egocentric space in the posterior parietal cortex
Stein, J. F. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00072605 · Cited by 339
Movement of Neural Activity on the Superior Colliculus Motor Map During Gaze Shifts
Munoz, D. P., Pélisson, D., & Guitton, D. (1991) · Science · doi:10.1126/science.2003221 · Cited by 310
Self-citationImplications of neural networks for how we think about brain function
Robinson, D. A. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00072563 · Cited by 107
Metadata
- Authors
- Guitton, D., Munoz, D. P., & Galiana, H. L.
- Venue
- Journal of Neurophysiology
- Publisher
- American Physiological Society
- Published
- 1990-08-01
- Volume
- 64
- Issue
- 2
- Pages
- 509-531
- ISSN
- 0022-3077 (ISSN-L)
- 1522-1598
- OpenAlex
- W2281361845
- Cited by
- 355
- References
- 61
- FWCI
- 37.74
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Gaze control in the cat: studies and modeling of the coupling between orienting eye and head movements in different behavioral tasks. https://app.cochat.ai/papers/10.1152/jn.1990.64.2.509
- The paper
- Guitton, D., Munoz, D. P., & Galiana, H. L. (1990). Gaze control in the cat: studies and modeling of the coupling between orienting eye and head movements in different behavioral tasks. Journal of Neurophysiology. https://doi.org/10.1152/jn.1990.64.2.509
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.