Cited by 244Fish biology, ecology, and behaviorMotor Control and AdaptationNeural dynamics and brain function

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An Efference Copy Which Is Modified by Reafferent Input

Bell, Curtis C.·1981·Science

DOI 10.1126/science.7291985

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Abstract

In electric fish of the mormyrid family, an efference copy is present in the brain region that receives afferent input from ampullary electroreceptors. The efference copy is elicited by the motor command to fire the electric organ. Its effect is always opposite that of ampullary afferents responding to the electric organ discharge, and it changes to match variations in this afferent input. It probably reduces the central effects of activity in ampullary receptors evoked by the electric organ discharge.

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Handbook of Sensory Physiology
Sanders, M. D. (1975) · British Journal of Ophthalmology · doi:10.1136/bjo.59.2.111-c · Cited by 7,166
Das Reafferenzprinzip: Wechselwirkungen zwischen Zentralnervensystem und Peripherie
von Holst, E., & Mittelstaedt, H. (1950) · Naturwissenschaften · doi:10.1007/bf00622503 · Cited by 2,655
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
Inhibition of afferent transmission in cuneate nucleus during voluntary movement in the cat
Ghez, C., & Pisa, M. (1972) · Brain Research · doi:10.1016/0006-8993(72)90120-5 · Cited by 254
Origin of modulation in neurones of the ventral spinocerebellar tract during locomotion
Arshavsky, Y. I., Berkinblit, M. B., Fukson, O. I., Gelfand, I. M., & Orlovsky, G. N. (1972) · Brain Research · doi:10.1016/0006-8993(72)90296-x · Cited by 184
Use of an extraretinal signal by monkey superior colliculus neurons to distinguish real from self-induced stimulus movement
Robinson, D. L., & Wurtz, R. H. (1976) · Journal of Neurophysiology · doi:10.1152/jn.1976.39.4.852 · Cited by 183
Habituation: Regulation through Presynaptic Inhibition
Krasne, F. B., & Bryan, J. S. (1973) · Science · doi:10.1126/science.182.4112.590 · Cited by 137
The Activity of Lateral-Line Efferent Neurones in Stationary and Swimming Dogfish
Roberts, B. L., & Russell, I. J. (1972) · Journal of Experimental Biology · doi:10.1242/jeb.57.2.435 · Cited by 137
Site of Neural Attenuation of Responses to Self-Vocalized Sounds in Echolocating Bats
Suga, N., & Shimozawa, T. (1974) · Science · doi:10.1126/science.183.4130.1211 · Cited by 110
Electroreception
Bennett, M. V. L. (1971) · Fish physiology · doi:10.1016/s1546-5098(08)60052-7 · Cited by 109

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BELL, C.C., SOCIETY FOR NEUROSCIENCE. ABSTRACTS 2: 177 (1976).
KALMIJN, A.J., HDB SENSORY PHYSIOLO 3: 147 (1974).
SZABO, T, HDB SENSORY PHYSIOLO 3: 13 (1974).
SZABO, T, HDB SENSORY PHYSL 3: 59 (1974).

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Authors: Bell, C. C.
Affiliations: Legacy Good Samaritan Medical Center (US)
Corresponding author: Bell, Curtis C.
Venue: Science
Publisher: American Association for the Advancement of Science (AAAS)
Published: 1981-10-23
Volume: 214
Issue: 4519
Pages: 450-453
ISSN: 0036-8075 (ISSN-L)
1095-9203
DOI: 10.1126/science.7291985
OpenAlex: W2063136300
Cited by: 244
References: 15
Citations by year: 2026: 8 · 2025: 5 · 2024: 4 · 2023: 6 · 2022: 5 · 2021: 9 · 2020: 26 · 2019: 6 · 2018: 9 · 2017: 7 · 2016: 6 · 2015: 7 · 2014: 11 · 2013: 5 · 2012: 11
FWCI: 30.20
Type: journal article
Language: en
Open access: closed
Locations: Science (publishedVersion)
PubMed (publishedVersion)
Topics: Physical Sciences › Environmental Science › Nature and Landscape Conservation › Fish biology, ecology, and behavior
Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Keywords: efference copy, ampullary electroreceptors, electric organ discharge, motor command, electroreception, sensory feedback
MeSH terms: Action Potentials, Afferent Pathways, Animals, Brain, Efferent Pathways, Electric Organ, Fishes, Proprioception

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An Efference Copy Which Is Modified by Reafferent Input

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