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Neural Mechanisms of Saccadic Suppression
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In normal vision our gaze leaps from detail to detail, resulting in rapid image motion across the retina. Yet we are unaware of such motion, a phenomenon known as saccadic suppression. We recorded neural activity in the middle temporal and middle superior temporal cortical areas during saccades and identical image motion under passive viewing conditions. Some neurons were selectively silenced during saccadic image motion, but responded well to identical external image motion. In addition, a subpopulation of neurons reversed their preferred direction of motion during saccades. Consequently, oppositely directed motion signals annul one another, and motion percepts are suppressed.
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“For example, during a saccade there is neither visual nor proprioceptive sensory feedback (Keller and Robinson, 1971; Guthrie et al., 1983; Thiele et al., 2002).”
From Cerebellum, Predictions and Errors (2019) · cites this paper as Thiele et al., 2002
Experimental — accuracy not yet measuredIn the citing paper
“Saccadic suppression mechanisms have been identified in a host of different species, such as pigeons, chickens, locusts, monkeys and cats34–38.”
From Corollary discharge across the animal kingdom (2008) · cites this paper as [36]
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Das Reafferenzprinzip: Wechselwirkungen zwischen Zentralnervensystem und Peripherie
von Holst, E., & Mittelstaedt, H. (1950) · Naturwissenschaften · doi:10.1007/bf00622503 · Cited by 2,655
The analysis of visual motion: a comparison of neuronal and psychophysical performance
Britten, K., Shadlen, M., Newsome, W., & Movshon, J. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-12-04745.1992 · Cited by 1,958
Attentional modulation of visual motion processing in cortical areas MT and MST
Treue, S., & Maunsell, J. H. R. (1996) · Nature · doi:10.1038/382539a0 · Cited by 1,025
Failure to detect displacement of the visual world during saccadic eye movements
Bridgeman, B., Hendry, D. P., & STARK, L. W. (1975) · Vision Research · doi:10.1016/0042-6989(75)90290-4 · Cited by 881
Saccadic suppression: A review and an analysis.
Matin, E. (1974) · Psychological Bulletin · doi:10.1037/h0037368 · Cited by 793
Selective suppression of the magnocellular visual pathway during saccadic eye movements
Burr, D. C., Morrone, M. C., & Ross, J. (1994) · Nature · doi:10.1038/371511a0 · Cited by 685
Contrast sensitivity at high velocities
Burr, D. C., & Ross, J. (1982) · Vision Research · doi:10.1016/0042-6989(82)90196-1 · Cited by 349
Saccadic omission: Why we do not see a grey-out during a saccadic eye movement
Campbell, F. W., & Wurtz, R. H. (1978) · Vision Research · doi:10.1016/0042-6989(78)90219-5 · Cited by 346
Extraretinal Control of Saccadic Suppression
Diamond, M. R., Ross, J., & Morrone, M. C. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-09-03449.2000 · Cited by 307
Celebrini, S., & Newsome, W. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-07-04109.1994 · Cited by 232
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Research works printed but not linked: 3
- Holt E., Harvard Psychol. Stud. 1, 3 (1903).
- Sperry R. W., Vision Res. 16, 1185 (1950).
- Supplementary Web material is available on Science Online at www.sciencemag.org/cgi/content/full/295/5564/2460/DC1.
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Metadata
- Authors
- Thiele, A., Henning, P., Kubischik, M., & Hoffmann, K.-P.
- Affiliations
- Ruhr University Bochum (DE)
- Corresponding author
- Thiele, A.
- Hoffmann, K.-P.
- ORCID
- Thiele, A.
- Venue
- Science
- Published
- 2002-03-29
- Volume
- 295
- Issue
- 5564
- Pages
- 2460-2462
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W1995699966
- Cited by
- 278
- References
- 26
- Citations by year
- 2026: 6 · 2025: 11 · 2024: 9 · 2023: 8 · 2022: 13 · 2021: 19 · 2020: 10 · 2019: 11 · 2018: 4 · 2017: 14 · 2016: 12 · 2015: 10 · 2014: 10 · 2013: 6 · 2012: 13
- FWCI
- 7.07
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Newcastle University ePrints (Newcastle Univesity)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Multisensory perception and integration
- Keywords
- saccadic suppression, saccades, middle temporal cortex, visual motion perception, neuronal silencing, direction-selective neurons
- MeSH terms
- Animals, Macaca mulatta, Motion Perception, Neurons, Perceptual Masking, Retina, Saccades, Temporal Lobe, Visual Pathways, Visual Perception
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 ›
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