bioRxiv Science⌕ Search

Biology subjects

Mipounga, H. K.

Publications and source records attributed to Mipounga, H. K..

2 recordsLinked to original sources

Electric signal polymorphism predicts dietary niche partitioning in a weakly electric fish

Electric organ discharge (EOD) waveform diversity in African elephantfish is often attributed to sexual selection, yet EODs also mediate active electrolocation during prey detection, raising the possibility that natural selection on foraging ecology contributes to waveform divergence. Paramormyrops kingsleyae exhibits an intraspecific polymorphism where certain populations emit biphasic EODs whereas other populations emit triphasic waveforms. The genes underlying this polymorphism show signatures of selection; the polymorphism persists despite gene flow and is behaviorally discriminable by the fish themselves. If waveform differences influence prey detection during active electrolocation, biphasic and triphasic fish should consume systematically different prey. We tested this prediction using DNA metabarcoding of gut contents from 186 mormyrids representing 16 species across eight sites in Gabon, employing two independent COI primer sets for cross-validation and pairing dietary data with environmental invertebrate sampling to distinguish active prey preference from passive availability. At the community level in the diverse Bale Creek mormyrid assemblage, species identity was the dominant predictor of diet composition (R{superscript 2} {approx} 24%), consistent with phylogenetic signal in foraging ecology. Within P. kingsleyae, waveform type was the strongest independent predictor of dietary composition (R{superscript 2} = 5-6%), explaining variance independently of geographic region, sex, body size, and parasitism status -- a result concordant across both primer sets. Dietary differences were driven by prey species turnover rather than differential abundance of shared prey, and prey selectivity analyses confirmed that waveform types differ in which prey they actively prefer, not merely in what is locally available. These findings are consistent with natural selection on foraging ecology contributing to the maintenance of EOD waveform polymorphism, though the sensory mechanisms linking subtle waveform differences to prey detection remain an open question.

ecology↗

The Genomic Basis of Electric Signal Diversity

Behavioral diversity is a striking result of species diversity, shaped by intertwined mechanisms, developmental pathways, and evolutionary histories. Yet the genetic underpinnings of behavioral evolution remain obscure, even though they are key to understanding how organisms adapt and diversify. Weakly electric African elephantfishes provide a rare opportunity to dissect the genetics of behavior because their electric communication signals are quantifiable, stereotyped, and directly tied to identifiable cellular mechanisms. Among elephantfishes, electric organ discharges (EODs) vary widely across species and populations, shaping mate choice, social interactions, and reproductive isolation. A key axis of this diversity is the presence or absence of an initial phase in the EOD waveform--a discrete, repeated evolutionary transition whose genetic basis has remained unresolved. Here we show, using whole-genome resequencing, population-genomic analyses, transcriptomics, and histology from 306 specimens, that biphasic EODs in Paramormyrops kingsleyae have evolved repeatedly through independent de novo regulatory mutations at distinct genomic loci. These population-specific mutations occur exclusively in noncoding regions, show localized signatures of selection, and are associated with differences in gene expression and protein localization in the electric organ, indicating that they act through cis-regulatory mechanisms affecting electrocyte development. These findings challenge the expectation that repeated within-species adaptations primarily draw from standing ancestral variation, revealing instead that the developmental program underlying electric signaling contains multiple points of regulatory sensitivity. Distinct genetic changes can therefore produce the same behavioral phenotype, enabling repeated evolutionary transitions even within a single species. More broadly, our results show how developmental architecture shapes the evolutionary pathways available to behavior, helping explain why communication signals in elephantfishes--and in other radiations--diversify so rapidly.

evolutionary biology↗