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Nelson, M. E. & MacIver, M. A. Sensory acquisition in active sensing systems. J. Comp. Physiol. A 192, 573–586 (2006).
Jones, T. K., Allen, K. M. & Moss, C. F. Communication with self, friends and foes in active-sensing animals. J. Exp. Biol. 224, jeb242637 (2021).
Heiligenberg, W. Neural Nets in Electric Fish (MIT Press, 1991).
Rose, G. J. Insights into neural mechanisms and evolution of behaviour from electric fish. Nat. Rev. Neurosci. 5, 943–951 (2004).
Braca, P., Goldhahn, R., Ferri, G. & LePage, K. D. Distributed information fusion in multistatic sensor networks for underwater surveillance. IEEE Sens. J. 16, 4003–4014 (2015).
Chernyak, V. S. Fundamentals of Multisite Radar Systems: Multistatic Radars and Multistatic Radar Systems (CRC, 1998).
Boyer, F., Lebastard, V., Chevallereau, C., Mintchev, S. & Stefanini, C. Underwater navigation based on passive electric sense: new perspectives for underwater docking. Int. J. Robot. Res. 34, 1228–1250 (2015).
Flohr, T. G. et al. Multi-detector row CT systems and image-reconstruction techniques. Radiology 235, 756–773 (2005).
Heiligenberg, W. Electrolocation jamming avoidance in the mormyrid fish Brienomyrus. J. Comp. Physiol. 109, 357–372 (1976).
Gregg, J. D., Dudzinski, K. M. & Smith, H. V. Do dolphins eavesdrop on the echolocation signals of conspecifics? Int. J. Comp. Psychol. 20 65–88 (2007).
Kuc, R. Object localization from acoustic emissions produced by other sonars (L). J. Acoust. Soc. Am. 112, 1753–1755 (2002).
Dechmann, D. K. et al. Experimental evidence for group hunting via eavesdropping in echolocating bats. Proc. Biol. Sci. 276, 2721–2728 (2009).
Götz, T., Verfuß, U. K. & Schnitzler, H.-U. ‘Eavesdropping’ in wild rough-toothed dolphins (Steno bredanensis)? Biol. Lett. 2, 5–7 (2006).
Chiu, C., Xian, W. & Moss, C. F. Flying in silence: echolocating bats cease vocalizing to avoid sonar jamming. Proc. Natl Acad. Sci. USA 105, 13116–13121 (2008).
Hopkins, C. D. Neuroethology of electric communication. Annu. Rev. Neurosci. 11, 497–535 (1988).
Bell, C. C. Sensory coding and corollary discharge effects in mormyrid electric fish. J. Exp. Biol. 146, 229–253 (1989).
Kawasaki, M. in Electroreception Springer Handbook of Auditory Research (eds Bullock, T. H. et al.) Ch. 7, 154–194 (Springer, 2005).
Rother, D. et al. Electric images of two low resistance objects in weakly electric fish. BioSystems 71, 169–177 (2003).
Bell, C. C. in Electroreception (eds Bullock, T. H. & Heiligenberg, W.) 423–452 (Wiley, 1986).
Fortune, E. S. The decoding of electrosensory systems. Curr. Opin. Neurobiol. 16, 474–480 (2006).
Push, S. & Moller, P. Spatial aspects of electrolocation in the mormyrid fish, Gnathonemus petersii. J. Physiol. 75, 355–357 (1979).
Pedraja, F., Hofmann, V., Goulet, J. & Engelmann, J. Task-related sensorimotor adjustments increase the sensory range in electrolocation. J. Neurosci. 40, 1097–1109 (2020).
Babineau, D., Longtin, A. & Lewis, J. E. Modeling the electric field of weakly electric fish. J. Exp. Biol. 209, 3636–3651 (2006).
von der Emde, G. & Schwarz, S. Imaging of objects through active electrolocation in Gnathonemus petersii. J. Physiol. 96, 431–444 (2002).
Chen, L., House, J. L., Krahe, R. & Nelson, M. E. Modeling signal and background components of electrosensory scenes. J. Comp. Physiol. A 191, 331–345 (2005).
Baker, C. A. & Carlson, B. A. Short-term depression, temporal summation, and onset inhibition shape interval tuning in midbrain neurons. J. Neurosci. 34, 14272–14287 (2014).
Xu-Friedman, M. A. & Hopkins, C. D. Central mechanisms of temporal analysis in the knollenorgan pathway of mormyrid electric fish. J. Exp. Biol. 202, 1311–1318 (1999).
Post, N. & von der Emde, G. The ‘novelty response’ in an electric fish: response properties and habituation. Physiol. Behav. 68, 115–128 (1999).
Enikolopov, A. G., Abbott, L. F. & Sawtell, N. B. Internally generated Predictions enhance neural and behavioral detection of sensory stimuli in an electric fish. Neuron 99, 135–146 (2018).
Worm, M. et al. Evidence for mutual allocation of social attention through interactive signaling in a mormyrid weakly electric fish. Proc. Natl Acad. Sci. USA 115, 6852–6857 (2018).
Moller, P. Electric Fishes: History and Behavior (Chapman and Hall, 1995).
Russell, C. J., Myers, J. P. & Bell, C. C. The echo response in Gnathonemus petersii. J. Comp. Physiol. 92, 181–200 (1974).
Kramer, B. Electric organ discharge interaction during interspecific agonistic behaviour in freely swimming mormyrid fish. A method to evaluate two or more. J. Comp. Physiol. 93, 203–236 (1974).
Lissmann, H. W. & Machin, K. E. The mechanism of object location in Gymnarchus niloticus and similar fish. J. Exp. Biol. 35, 451–486 (1958).
von der Emde, G. Discrimination of objects through electrolocation in the weakly electric fish, Gnathonemus petersii. J. Comp. Physiol. A 167, 413–421 (1990).
Hall, J. C., Bell, C. & Zelick, R. Behavioral evidence of a latency code for stimulus intensity in mormyrid electric fish. J. Comp Physiol. A 177, 29–39 (1995).
Bell, C. C. Mormyromast electroreceptor organs and their afferents in mormyrid electric fish: III. Physiological differences between two morphological types of fibers. J. Neurophysiol. 63, 319–332 (1990).
Toerring, M. J. & Moller, P. Locomotor and electric displays associated with electrolocation during exploratory behavior in mormyrid fish. Behav. Brain Res. 12, 291–306 (1984).
Russell, C. J. & Bell, C. C. Neuronal responses to electrosensory input in the mormyrid valvula cerebelli. J. Neurophysiol. 41, 1495–1510 (1978).
Sawtell, N. B., Mohr, C. & Bell, C. C. Recurrent feedback in the mormyrid electrosensory system: cells of the preeminential and lateral toral nuclei. J. Neurophysiol. 93, 2090–2103 (2005).
Prechtl, J. C. et al. Sensory processing in the pallium of a mormyrid fish. J. Neurosci. 18, 7381–7393 (1998).
Berdahl, A., Torney, C. J., Ioannou, C. C., Faria, J. J. & Couzin, I. D. Emergent sensing of complex environments by mobile animal groups. Science 339, 574–576 (2013).
Moller, P. Electric signals and schooling behavior in a weakly electric fish, Marcusenius cyprinoides L. (Mormyriformes). Science 193, 697–699 (1976).
Worm, M., Kirschbaum, F. & von der Emde, G. Social interactions between live and artificial weakly electric fish: electrocommunication and locomotor behavior of Mormyrus rume proboscirostris towards a mobile dummy fish. PLoS ONE 12, e0184622 (2017).
Gebhardt, K., Alt, W. & von der Emde, G. Electric discharge patterns in group-living weakly electric fish, Mormyrus rume (Mormyridae, Teleostei). Behaviour 149, 623–644 (2012).
Schuster, S. Count and spark? The echo response of the weakly electric fish Gnathonemus petersii to series of pulses. J. Exp. Biol. 204, 1401–1412 (2001).
Bell, C. C., Han, V. & Sawtell, N. B. Cerebellum-like structures and their implications for cerebellar function. Annu. Rev. Neurosci. 31, 1–24 (2008).
Nieuwenhuys, R. & Nicholson, C. in Neurobiology of Cerebellar Evolution and Development (ed. Llinas, R.) 107–134 (Am. Med. Assoc, 1969).
Sukhum, K. V., Shen, J. & Carlson, B. A. Extreme enlargement of the cerebellum in a clade of teleost fishes that evolved a novel active sensory system. Curr. Biol. 28, 3857–3863 (2018).
Finger, T. E., Bell, C. C. & Russell, C. J. Electrosensory pathways to the valvula cerebelli in mormyrid fish. Exp. Brain Res. 42, 23–33 (1981).
Bell, C. C., Myers, J. P. & Russell, C. J. Electric organ discharge patterns during dominance related behavioral displays in Gnathonemus petersii (Mormyridae). J. Comp. Physiol. 92, 201–228 (1974).
Mathis, A. et al. DeepLabCut: markerless pose estimation of user-defined body parts with deep learning. Nat. Neurosci. 21, 1281–1289 (2018).
Arthur, D. & Vassilvitskii, S. k-means++: the advantages of careful seeding. In Proc. 18th Annual ACM-SIAM Symposium on Discrete Algorithms, SODA’07, 1027–1035 (SIAM, 2007).
Braun, E., Geurten, B. & Egelhaaf, M. Identifying prototypical components in behaviour using clustering algorithms. PLoS ONE 5, e9361 (2010).
Migliaro, A., Caputi, A. A. & Budelli, R. Theoretical analysis of pre-receptor image conditioning in weakly electric fish. PLoS Comput. Biol. 1, 123–131 (2005).
Engelmann, J., Bacelo, J., van den, B. E. & Grant, K. Sensory and motor effects of etomidate anesthesia. J. Neurophysiol. 95, 1231–1243 (2006).
Requarth, T. & Sawtell, N. B. Plastic corollary discharge predicts sensory consequences of movements in a cerebellum-like circuit. Neuron 82, 896–907 (2014).
Bell, C. C., Grant, K. & Serrier, J. Corollary discharge effects and sensory processing in the mormyrid electrosensory lobe: I. Field potentials and cellular activity in associated structures. J. Neurophysiol. 68, 843–858 (1992).
Bell, C. C., Caputi, A. & Grant, K. Physiology and plasticity of morphologically identified cells in the mormyrid electrosensory lobe. J. Neurosci. 17, 6409–6422 (1997).
Mohr, C., Roberts, P. D. & Bell, C. C. Cells of the mormyromast region of the mormyrid electrosensory lobe: I. Responses to the electric organ corollary discharge and to electrosensory stimuli. J. Neurophysiol. 90, 1193–1210 (2003).
Kobak, D. et al. Demixed principal component analysis of neural population data. eLife 5, e10989 (2016).
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