Fish sounds are known to be species-specific, possessing unique temporal and spectral features. We have recorded and compared sounds in eight piranha species to evaluate the potential role of acoustic communication as a driving force in clade diversification. All piranha species showed the same kind of sound-producing mechanism: sonic muscles originate on vertebrae and attach to a tendon surrounding the bladder ventrally. Contractions of the sound-producing muscles force swimbladder vibration and dictate the fundamental frequency. It results the calling features of the eight piranha species logically share many common characteristics. In all the species, the calls are harmonic sounds composed of multiple continuous cycles. However, the sounds of Serrasalmus elongatus (higher number of cycles and high fundamental frequency) and S. manueli (long cycle periods and low fundamental frequency) are clearly distinguishable from the other species. The sonic mechanism being largely conserved throughout piranha evolution, acoustic communication can hardly be considered as the main driving force in the diversification process. However, sounds of some species are clearly distinguishable despite the short space for variations supporting the need for specific communication. Behavioural studies are needed to clearly understand the eventual role of the calls during spawning events.
Among piranhas, sound production is known in carnivorous species, whereas herbivorous species were thought to be mute. Given that these carnivorous sonic species have a complex sonic apparatus, we hypothesize that intermediate forms could be found in other serrasalmid species. The results highlight the evolutionary transition from a simple sound-producing mechanism without specialized sonic structures to a sonic mechanism involving large, fast-contracting sonic muscles. Hypaxial muscles in basal herbivores primarily serve locomotion, but some fibres cause sound production during swimming accelerations, meaning that these muscles have gained a dual function. Sound production therefore seems to have been acquired through exaptation, i.e. the development of a new function (sound production) in existing structures initially shaped for a different purpose (locomotion). In more derived species (Catoprion and Pygopristis), some fibres are distinguishable from typical hypaxial muscles and insert directly on the swimbladder. At this stage, the primary function (locomotion) is lost in favour of the secondary function (sound production). In the last stage, the muscles and insertion sites are larger and the innervation involves more spinal nerves, improving calling abilities. In serrasalmids, the evolution of acoustic communication is characterized initially by exaptation followed by adaptive evolution.
Like all otophysan fishes, serrasalmids (piranhas and relatives) possess a Weberian apparatus that improves their hearing capacities. We compared the hearing abilities among eight species of serrasalmids having different life-history traits: herbivorous vs. carnivorous and vocal vs. mute species. We also made 3D reconstructions of the auditory system to detect potential morphological variations associated with hearing ability. The hearing structures were similar in overall shape and position. All the species hear in the same frequency range and only slight differences were found in hearing thresholds. The eight species have their range of best hearing in the lower frequencies (50–900 Hz). In vocal serrasalmids, the range of best hearing covers the frequency spectrum of their sounds. However, the broad overlap in hearing thresholds among species having different life-history traits (herbivorous vs. carnivorous and vocal vs. non-vocal species) suggests that hearing ability is likely not related to the capacity to emit acoustic signals or to the diet, i.e. the ability to detect sounds is not associated with a given kind of food. The inner ear appears to be highly conservative in this group suggesting that it is shaped by phylogenetic history or by other kinds of constraints such as predator avoidance.
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