Saccadic suppression by corollary discharge in the locust
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Saccadic suppression mechanisms have been identified in pigeons, chickens, locusts, monkeys and cats.
“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 [35]
Cites
Plum, F. (1960) · Archives of Neurology · doi:10.1001/archneur.1960.03840090124020 · Cited by 10,377 · see citing works
Das Reafferenzprinzip: Wechselwirkungen zwischen Zentralnervensystem und Peripherie
von Holst, E., & Mittelstaedt, H. (1950) · Naturwissenschaften · doi:10.1007/bf00622503 · Cited by 2,655 · see citing works
Neural basis of the spontaneous optokinetic response produced by visual inversion
Sperry, R. W. (1950) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0055479 · Cited by 1,789 · see citing works
The mechanics of human saccadic eye movement
Robinson, D. A. (1964) · The Journal of Physiology · doi:10.1113/jphysiol.1964.sp007485 · Cited by 893 · see citing works
Saccadic suppression: A review and an analysis.
Matin, E. (1974) · Psychological Bulletin · doi:10.1037/h0037368 · Cited by 793 · see citing works
Benevento, L. A., & Rezak, M. (1976) · Brain Research · doi:10.1016/0006-8993(76)90160-8 · Cited by 370 · see citing works
MECHANISM OF SACCADIC EYE MOVEMENTS
Westheimer, G. (1954) · Archives of Ophthalmology · doi:10.1001/archopht.1954.00920050716006 · Cited by 363 · see citing works
Kuffler, S. W., Hunt, C. C., & QUILLIAM, J. P. (1951) · Journal of Neurophysiology · doi:10.1152/jn.1951.14.1.29 · Cited by 337 · see citing works
The orthopteran descending movement detector (DMD) neurones: a characterisation and review
Rowell, C. H. F. (1971) · Journal of Comparative Physiology A · doi:10.1007/bf00304131 · Cited by 212 · see citing works
Self-citationRobinson, D. L., & Wurtz, R. H. (1976) · Journal of Neurophysiology · doi:10.1152/jn.1976.39.4.852 · Cited by 183 · see citing works
The Neuronal Basis of A Sensory Analyser, The Acridid Movement Detector System
Rowell, C. H. F., O’shea, M., & Williams, J. L. D. (1977) · Journal of Experimental Biology · doi:10.1242/jeb.68.1.157 · Cited by 177 · see citing works
Self-citationConnections between descending visual interneurons and metathoracic motoneurons in the locust
Burrows, M., & Rowell, C. H. F. (1973) · Journal of Comparative Physiology A · doi:10.1007/bf00694231 · Cited by 148 · see citing works
Self-citationSuppression of visual phosphenes during saccadic eye movements
Riggs, L. A., Merton, P. A., & Morton, H. (1974) · Vision Research · doi:10.1016/0042-6989(74)90169-2 · Cited by 146 · see citing works
Response of striate cortex neurons to stimuli during rapid eye movements in the monkey.
Wurtz, R. H. (1969) · Journal of Neurophysiology · doi:10.1152/jn.1969.32.6.975 · Cited by 138 · see citing works
Goodman, L. J. (1965) · Journal of Experimental Biology · doi:10.1242/jeb.42.3.385 · Cited by 131 · see citing works
Pearson, K. G., & Goodman, C. S. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901840109 · Cited by 114 · see citing works
A sensitive position measuring device for biological systems
Sandeman, D. C. (1968) · Comparative Biochemistry and Physiology · doi:10.1016/0010-406x(68)91017-7 · Cited by 101 · see citing works
Protection from habituation by lateral inhibition
O’Shea, M., & Rowell, C. H. F. (1975) · Nature · doi:10.1038/254053a0 · Cited by 96 · see citing works
Self-citationThe post‐synaptic action of efferent fibres in the lateral line organ of the burbot Lota lota
Flock, Å., & Russell, I. J. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010406 · Cited by 94 · see citing works
An inhibitory process influencing visual responses in a fibre of the ventral nerve cord of locusts
Palka, J. (1967) · Journal of Insect Physiology · doi:10.1016/0022-1910(67)90151-5 · Cited by 88 · see citing works
Medium and Long-Term Changes in the Behaviour of Visual Neurones in the Tritocerebrum of Locusts
Horn, G., & Rowell, C. H. F. (1968) · Journal of Experimental Biology · doi:10.1242/jeb.49.1.143 · Cited by 69 · see citing works
Self-citationNoda, H. (1975) · The Journal of Physiology · doi:10.1113/jphysiol.1975.sp011004 · Cited by 59 · see citing works
Hair Receptors in Locusts: Hair Plates on the First Cervical Sclerites of the Orthoptera
Goodman, L. J. (1959) · Nature · doi:10.1038/1831106a0 · Cited by 50 · see citing works
Discrimination Between Movements of Eye and Object by Visual Interneurones of Crickets
Palka, J. (1969) · Journal of Experimental Biology · doi:10.1242/jeb.50.3.723 · Cited by 50 · see citing works
Rowell, C. H. F., & O’Shea, M. (1976) · Journal of Experimental Biology · doi:10.1242/jeb.65.2.273 · Cited by 41 · see citing works
Self-citationControl of Head Movement in the Locust, Schistocerca Gregaria
Shepheard, P. (1974) · Journal of Experimental Biology · doi:10.1242/jeb.60.3.735 · Cited by 41 · see citing works
Changes in visual evoked responses during the fast phase of optokinetic nystagmus in the rabbit
Collewijn, H. (1969) · Vision Research · doi:10.1016/0042-6989(69)90016-9 · Cited by 37 · see citing works
Hair Receptors in Locusts: Function of certain Prothoracic Hair Receptors in the Desert Locust
Haskell, P. T. (1959) · Nature · doi:10.1038/1831107a0 · Cited by 24 · see citing works
The fast phase of optokinetic nystagmus in the locust
Kien, J., & Land, M. F. (1978) · Physiological Entomology · doi:10.1111/j.1365-3032.1978.tb00132.x · Cited by 23 · see citing works
Comparison of sensory input with motor output in the locust optomotor system
Kien, J. (1977) · Journal of Comparative Physiology A · doi:10.1007/bf00611987 · Cited by 20 · see citing works
Neural pathways common to vestibular and optokinetic eye movements
Wallace, M. T., Blair, S. M., & Westheimer, G. (1978) · Experimental Brain Research · doi:10.1007/bf00238791 · Cited by 10 · see citing works
(1967) · American Zoologist · doi:10.1093/icb/7.1.7 · Cited by 1 · see citing works
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Grush, R. (2004) · Behavioral and Brain Sciences · doi:10.1017/s0140525x04000093 · Cited by 1,387 · see citing works
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Stephan, K. E., Friston, K. J., & Frith, C. D. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn176 · Cited by 1,134 · see citing works
Corollary discharge across the animal kingdom
Crapse, T. B., & Sommer, M. A. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2457 · Cited by 789 · see citing works
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Poulet, J. F. A., & Hedwig, B. (2006) · Science · doi:10.1126/science.1120847 · Cited by 234 · see citing works
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- Authors
- ZARETSKY, M., & ROWELL, C. H. F.
- Affiliations
- University of California, San Francisco (US)
- University of California, Berkeley (US)
- ORCID
- ROWELL, C. H. FRASER
- Venue
- Nature
- Published
- 1979-08
- Volume
- 280
- Issue
- 5723
- Pages
- 583-585
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2020657632
- Cited by
- 58
- References
- 32
- Citations by year
- 2025: 2 · 2023: 1 · 2022: 1 · 2021: 1 · 2020: 2 · 2018: 1 · 2017: 2 · 2016: 1 · 2015: 1 · 2014: 4 · 2013: 2 · 2012: 2
- FWCI
- 1.37
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Keywords
- saccadic suppression, corollary discharge, efference copy, locusts, eye movements, optokinetic nystagmus, retinal image displacement, visual perception, head movement, insect vision
- MeSH terms
- Action Potentials, Animals, Brain, Eye Movements, Grasshoppers, Motion Perception, Neural Inhibition, Saccades, Visual Perception
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