ArticleeLife2016
Detection of transient synchrony across oscillating receptors by the central electrosensory system of mormyrid fish.
Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- Developmental and evolutionary changes in sensorimotor integration to maintain coordination of corollary discharge and afferent input in electric fish.Current biology : CB · 2026Article
- Signal Diversification Is Associated with Corollary Discharge Evolution in Weakly Electric Fish.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020Article
- A History of Corollary Discharge: Contributions of Mormyrid Weakly Electric Fish.Frontiers in integrative neuroscience · 2020Review
- The cellular and circuit basis for evolutionary change in sensory perception in mormyrid fishes.Scientific reports · 2017Article
- Electrosensory processing in Apteronotus albifrons: implications for general and specific neural coding strategies across wave-type weakly electric fish species.Journal of neurophysiology · 2016Article
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Authors and funding
2 authors.
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Abstract
Recently, we reported evidence for a novel mechanism of peripheral sensory coding based on oscillatory synchrony. Spontaneously oscillating electroreceptors in weakly electric fish (Mormyridae) respond to electrosensory stimuli with a phase reset that results in transient synchrony across the receptor population (Baker et al., 2015). Here, we asked whether the central electrosensory system actually detects the occurrence of synchronous oscillations among receptors. We found that electrosensory stimulation elicited evoked potentials in the midbrain exterolateral nucleus at a short latency following receptor synchronization. Frequency tuning in the midbrain resembled peripheral frequency tuning, which matches the intrinsic oscillation frequencies of the receptors. These frequencies are lower than those in individual conspecific signals, and instead match those found in collective signals produced by groups of conspecifics. Our results provide further support for a novel mechanism for sensory coding based on the detection of oscillatory synchrony among peripheral receptors.
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