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.
The ability to discriminate both biotic and abiotic sound sources is crucial for fishes1. They possess hearing structures that enable them to detect and identify different kinds of sounds in their environment, including conspecific calls, sounds produced by prey and predators, or abiotic cues that convey information on the environment1,2,3,4,5,6,7.
According to Ladich (2014)8, all fish species possess inner ears for sound detection but not all species possess sound generating mechanisms. This suggests that acoustic communication is not the primary constraint acting on the evolution of inner ears. Other life-history traits (diet, background noise, etc.) could correlate with differences in hearing ability. Serrasalmidae is an ideal family to examine co-variation in hearing and life-history traits because this family includes species that share different features: sound production vs. mute species and herbivorous vs. carnivorous species.
The Ostariophysan subgroup Otophysi is characterized by a series of modified elements (modifications of the first vertebrae, of the endo- and perilymphatic spaces of the inner ears and modifications of the swimbladder), called the Weberian apparatus, that connect the swimbladder to the inner ears9,10,11,12,13. The Weberian apparatus consists of paired symmetrical chains composed of one to four Weberian ossicles (tripus, intercalarium, scaphium and claustrum) that lie in a linear sequence from the swimbladder to the inner ear. Interossicular ligaments and articulation of the Weberian ossicles with their respective centra allow ossicles to hold in position on each side of the vertebral column14. Von Frisch (1938)15 demonstrated that these ossicular chains function in sound transmission. However, the claustrum is no longer considered as having an auditory function, at least in characiforms and siluriforms. In these groups, it has a protective function of the anterior portion of the neural canal16,17. When the swimbladder vibrates in a sound field, vibrations are transmitted to the ossicles and this motion is transmitted to the endolymphatic fluid causing sagitta (saccular otolith) displacements18,19.
Several studies have highlighted the important role of the Weberian apparatus in the improvement of hearing abilities, in terms of both hearing bandwidth and auditory sensitivity12,20,21. Ladich and Wysocki (2003)22 demonstrated that bilateral extirpation of the tripus in the otophysan Carassius auratus, goldfish, resulted in a hearing loss ranging from 7 dB at 100 Hz to 33 dB at 2 kHz. Yan et al. (2000)23 showed that the deflation of the swimbladder in the goldfish caused a drop in sensitivity by 33 to 55 dB depending on the frequency. However, otophysans do not exhibit a common morphology of the Weberian apparatus and swimbladder and this variation seems to have an impact on hearing ability. In catfishes, larger swimbladders and Weberian ossicles as well as greater numbers of ossicles are associated with improved hearing capacities24.
Our study focuses on the hearing abilities of eight species in the family Serrasalmidae. Four species are classified as leaf, fruit, or seed-eating25,26,27: Piaractus brachypomus (Cuvier, 1818); Metynnis lippincottianus (Cope, 1870); Myloplus rubripinnis (Müller and Troschel, 1844) and Myleus schomburgkii (Jardine, 1841). The other four, Serrasalmus elongatus Kner, 1858; Serrasalmus spilopleura Kner, 1858; Pygocentrus nattereri Kner, 1858 and Pygocentrus piraya (Cuvier, 1819), are classified as carnivorous piranhas28,29. Moreover, we note that five of these species are known to produce sounds. Serrasalmus elongatus, S. spilopleura and Py. nattereri emit low frequency sounds by contracting fast sonic muscles attached to the anterior chamber of the swimbladder30,31,32. Piaractus brachypomus and Pygocentrus piraya are also able to produce low frequency calls (unpublished data). The first goal of our study was to determine hearing capacities of these eight species and to investigate co-variation in hearing abilities and life-history traits (carnivorous vs. herbivorous and vocal vs. non-vocal species). The second objective was to compare the morphology of hearing structures among the species and to evaluate if morphological variation may explain differences in hearing abilities. Our hypothesis is that vocal species as well as carnivorous piranhas would have better hearing abilities to optimize intraspecific acoustic communication and to localize their living prey, respectively.
Auditory evoked potentials (AEP) were obtained for the eight serrasalmid species. AEP traces were similar in shape within a given frequency across all individuals (Fig. 1). Waveforms produced in response to stimulus presentation decreased in magnitude as the sound pressure level decreased, and were used to determine AEP thresholds of the eight species (Fig. 1).
Five species out of eight were able to detect frequencies ranging from 50 to 3600 Hz (Fig. 2). Serrasalmus elongatus detects frequencies up to 3300 Hz, whereas the frequency range of Myloplus rubripinnis and Pygocentrus piraya extends up to 3000 Hz. The eight serrasalmid species were most sensitive at the lower frequencies tested, between about 50 and 900 Hz (Fig. 2). The eight species are characterized by the presence of a peak (at 2100 Hz or 2400 Hz according to the species) in their hearing curve. This high-frequency peak is particularly marked in M. rubripinnis and Py. piraya (Fig. 2, Table 1). Hearing thresholds of all species increase from 600 Hz to this peak (at 2100 Hz or 2400 Hz) and then decrease in higher frequencies (from 2400 Hz to 3000 Hz). Statistical tests (nested ANOVA, P < 0.001) revealed a significant species effect on AEP thresholds (Table 2). Post hoc tests (Tukey’s HSD) showed that, even if significant differences in auditory thresholds exist among certain species at certain frequencies, there is no clear distinction among the species over the entire frequency range (see Supplementary Table S1 for a detailed comparison among species). The two species that differed most in terms of auditory sensitivity are Pi. brachypomus and Py. nattereri. Pygocentrus nattereri was significantly more sensitive than Pi. brachypomus at 300 Hz, 900 Hz, 1200 Hz, 1500 Hz, 1800 Hz, 2100 Hz and 2400 Hz (P ≤ 0.001). At 1200 Hz, the difference of sensitivity exceeded 27 dB SPL (Table 1). The other serrasalmids possessed intermediate auditory thresholds between these two species for the majority of the frequencies tested.
The hearing range among herbivores (Pi. brachypomus, M. lippincottianus, M. rubripinnis and M. schomburgkii) and carnivores (S. elongatus, S. spilopleura, Py. nattereri and Py. piraya) largely overlapped (Fig. 3). Similarly, the hearing range of vocal (Pi. brachypomus, S. elongatus, S. spilopleura, Py. nattereri and Py. piraya) and non-vocal species (M. lippincottianus, M. rubripinnis and M. schomburgkii) also largely overlapped (Fig. 4). For the eight serrasalmid species, linear regressions were performed between fish SL and hearing thresholds at each frequency tested. There were no significant correlations between fish size and hearing sensitivity for any species (see Supplementary Table S2).
The structures of interest (otoliths, Weberian ossicles and the anterior swimbladder chamber) were described by means of three-dimensional reconstructions based on CT scans. Two species, Pygocentrus nattereri and Piaractus brachypomus, were selected for illustration because they show the greatest differences in hearing sensitivity (Figs 5 and 6).
The position and overall shape of the auditory structures were largely similar in the six species investigated (Py. nattereri, Pi. brachypomus, M. rubripinnis, M. schomburgkii, S. elongatus and M. lippincottianus). The asteriscus (lagenar otolith) was the most voluminous otolith, with a mean value between 58.7% and 85.7% of total otolith volume (Figs 5, 6). The lapillus (utricular otolith) was the second most voluminous (mean value between 9.5% and 39% of total otolith volume) and the sagitta (saccular otolith) was least voluminous (mean value between 2.3% and 6.9% of the total otolith volume; see Supplementary Table S3 for detailed morphological data of otoliths). Pygocentrus nattereri possessed the least voluminous sagittae (2.3% of the total otolith volume) and Pi. brachypomus the most voluminous (6.9% of the total otolith volume). The overall shape and location of the three pairs of otoliths in the neurocranium were similar in the six species (Figs 5, 6). The semicircular canals were not visible on CT scans.
The number of ossicles in the Weberian apparatus was the same in the six species (Figs 5, 6). Each species possessed a tripus, an intercalarium, a scaphium and a claustrum. The tripus was the largest Weberian ossicle in the six species, with a mean value between 73.5% and 81.8% of the total Weberian ossicle volume. As revealed by the reconstructions based on CT scans, the tripus contacts the anterior part of the swimbladder (Fig. 5a,d). Pygocentrus nattereri was characterized by the most voluminous anterior swimbladder (88.6% of the total swimbladder volume; see Supplementary Table S4 for detailed morphological data of Weberian ossicles and swimbladder). Volume and overall aspect and form of the Weberian ossicles were similar in the six serrasalmid species. However, some features presented slight differences among the species investigated. For example, Piaractus brachypomus has a tripus that is not as a laterally expanded compared to the other species. Piaractus brachypomus also has a wider lateral process on the intercalarium than the other species. For the scaphium, there is variation in the shape of the anterior margin of the concha scaphium (it is more rounded and extended in the piranhas and Metynnis) and the ascending process is shorter in the piranha species (Py. nattereri and S. elongatus).
For each hearing structure (otoliths, Weberian ossicles and the anterior swimbladder), linear regressions were performed between the averaged relative morphological measurements of the structure and hearing thresholds at each frequency tested. No clear relationship between the morphology of these structures and hearing sensitivity was observed in serrasalmids (see Supplementary Table S5 for detailed results of the regressions). When we looked for trends between morphology and hearing sensitivity at three larger frequency bands (50–1200 Hz, 1500–2400 Hz and 2700–3600 Hz), we observed an association between sagittal morphology and hearing sensitivity in high frequencies (2700–3600 Hz). The larger the sagitta, the lower the hearing sensitivity for high frequencies (relative length: R² = 0.781, P = 0.0195; relative volume: R² = 0.739, P = 0.028; relative surface area: R² = 0.914, P = 0.003; see Supplementary Table S6 for detailed results of the regressions).
The Weberian apparatus is well-known to improve hearing abilities of otophysan fishes, in terms of both hearing bandwidth and hearing sensitivity20,21. The eight serrasalmid species investigated in our study were able to detect frequencies up to at least 3000 Hz which is common to Otophysi19,22,33,34. Surprisingly, all species were characterized by a low sensitivity peak in their audiogram (around 2400 Hz) followed by an increase in sensitivity in higher frequencies. Comparisons of AEP audiograms showed few differences in mean hearing thresholds among the studied species.
All the species had their best hearing sensitivity in the low frequencies (50–900 Hz). Stabentheiner (1988)35 previously determined the hearing thresholds of Pygocentrus nattereri by means of a behavioral method. He found that the highest sensitivity was between 100 and 600 Hz. He noted that the range of best hearing covers the frequency spectrum of drumming sounds produced by this species. This is also the case for the vocal species investigated in our study. Sounds emitted by S. elongatus, S. spilopleura, Py. nattereri and Py. piraya have a fundamental frequency between 100 and 200 Hz and contain harmonics30,31,32, whereas sounds produced by Pi. brachypomus have a dominant frequency around 80 Hz without harmonics (personal observations; unpublished data). We infer that vocal serrasalmid species used structures to produce sounds within the hearing range in which they hear best. However, the hearing thresholds of non-vocal species are similar to the hearing thresholds of vocal species (Fig. 4). This indicates that hearing capacities in serrasalmids are not related to the ability to produce sounds. Although previous comparisons did not concern species of the same taxa, it was previously hypothesized that selective pressures might be related to other relevant acoustic cues, such as predator and food detection in quiet freshwater habitats2,36. The auditory system of both vocal and non-vocal fish species from different taxa can possess high temporal resolution abilities, reinforcing the idea that the primary function of acute hearing may not be acoustic communication37. As in Serrasalmidae, Ladich and Popper (2001)38 showed that three species of acanthomorph labyrinth fishes (gouramis) differing widely in their abilities to produce sounds possessed similar auditory sensitivity and similar sensory epithelia morphology.
Food and prey detection could also act as selective pressures on hearing abilities of fishes2,36. A splashing noise emitted by a hurt fish swimming near the water surface is known to attract carnivorous piranhas and to motivate them to attack39. Herbivorous serrasalmids primarily eat seeds and fruits25,26,27. Consequently one could expect that their hearing abilities, in addition to their lateral line system, might allow them to detect these items falling into the water. However, the range of hearing thresholds of herbivorous and carnivorous species strongly overlapped (Fig. 3) and the range is not obviously related to the detection of food items.
The number of ossicles comprising the Weberian apparatus was the same in each species and the overall shape and position of these ossicles were quite comparable, despite slight morphological variation among the species. The otoliths were also similar in overall shape and position. We found an association between sagittal morphology and hearing sensitivity at the highest frequencies tested (2700–3600 Hz). Small sagittae are correlated with low hearing thresholds (i.e. better hearing abilities). Chardon and Vandewalle (1997)12 hypothesized that smaller sagittae in otophysans would reduce inertia to detect the small fluid movements transduced from the Weberian ossicles. Based on this hypothesis, we would expect lower mass sagittae to be associated with high hearing sensitivity. In fact, species with the best hearing sensitivity (in the frequency range 2700–3600 Hz) in our study possessed the smallest sagittae. However, further studies using microphonics, an electrophysiological recording technique, are needed to test experimentally the influence of sagittal morphology on high frequencies sensitivity40,41. It is also worth mentioning that the majority of significant hearing differences among serrasalmids were observed in the frequency range 900–2400 Hz. These hearing differences were not correlated with observed morphological variation.
The slight differences in hearing sensitivity among the species investigated in our study could be due to more subtle morphological variation. For example, the slight morphological disparities observed in tripus shape or in the length of ossicles processes could influence hearing sensitivity. Moreover, the orientation patterns of ciliary bundles of the sensory hair cells on the maculae (sensory epithelia associated with the otoliths) could also have an impact on the acoustic abilities in fishes42,43,44. Unfortunately, these last structures were not visible on the µCT scans and were not reconstructed.
Morphological variation of the Weberian apparatus within a single fish family has rarely been studied. Within the otophysan Cypriniformes, the morphology of the Weberian apparatus is generally diagnostic for each family and only slight interspecific variations of the Weberian apparatus have been documented. These modifications comprised subtle changes in shape and length of Weberian ossicle processes (e.g. Bird and Hernandez)45. Contrary to Cypriniformes, the diversity in swimbladder and Weberian apparatus morphology in the otophysan Siluriformes (catfishes) is high. Lechner and Ladich (2008)24 showed that larger swimbladders and ossicles as well as higher ossicle number (i.e. less evolutionary loss of ossicles) improve hearing at higher frequencies in catfishes. The relative lengths of swimbladders and of ossicular chains were correlated with hearing sensitivity above 1 and 2 kHz, respectively, whereas the number of ossicles affected hearing at 4 and 5 kHz. In our study, the number and the morphology of Weberian ossicles were conserved among the species and did not have an obvious impact on hearing abilities.
The size ranges of the different species indicate that the majority of specimens were juveniles or subadults. Hearing range and auditory sensitivity are known to increase along with the development of the auditory structures20,21. In the goldfish Carassius auratus, the Weberian apparatus reaches the adult condition at 25 mm length46. In the African bullhead catfish Lophiobagrus cyclurus, Weberian ossicles and ligaments are fully developed at 24 mm SL21, whereas ossicles are fully developed at 15 mm TL in the air-breathing catfish, Clarias gariepinnus47. According to the size of serrasalmid specimens used in AEP experiments, they all have a completely developed Weberian apparatus meaning the ear is fully functional. Although it is not always the case10,20,48, hearing sensitivity could potentially change with fish size, as in the catfish L. cyclurus that showed significant frequency-dependent change in hearing thresholds with size but no change in the range of detectable frequencies.
It is worth mentioning that there are a number of rheophilic serrasalmid species which were not included in this study49,50. Some authors hypothesized that hearing in fish may be adapted to the ambient noise of the fish’s habitat8,51. Since rheophilic species live in noisy rapids, it would be quite interesting to determine if their hearing abilities and the morphology of their auditory system vary compared to serrasalmid species living in quieter freshwater habitats.
In serrasalmids, the broad overlap in hearing ability among species having different life-history traits (vocal vs. non-vocal and herbivorous vs. carnivorous) suggests that hearing capacities are likely not related to the ability to produce sounds nor to food detection. The morphology of otoliths and Weberian apparatus is largely similar in the species investigated and does not explain obviously differences in hearing abilities. The slight differences in hearing thresholds among the species could be related to more subtle differences in shape and functional performance of the different Weberian ossicles or to variations in the shape of maculae or in the orientation patterns of ciliary hair cells on sensory epithelia.
Ten Piaractus brachypomus (69 to 95 mm SL), 10 Metynnis lippincottianus (76 to 87 mm SL), 3 Myloplus rubripinnis (98 to 108 mm SL), 8 Myleus schomburgkii (55 to 61 mm SL), 5 Serrasalmus elongatus (66 to 79 mm SL), 7 Serrasalmus spilopleura (75 to 105 mm SL), 10 Pygocentrus nattereri (64 to 70 mm SL) and 5 Pygocentrus piraya (96 to 112 mm SL) were purchased in the aquarium trade. They were housed in freshwater aquaria at 26 ± 1 °C and were maintained on a 12 h light/dark cycle. The tanks were equipped with external filters, internal heaters and bubblers for aeration. Herbivorous fishes were fed granule food (JBL Novo Tab), whereas flesh-eating species were fed mussels, three times a week. All procedures were approved by the ethical commission of the University of Liège (ethics case 1532).
AEP thresholds measurement: experimental setup
Hearing thresholds were measured using the AEP technique52,53. This technique records summation of acoustically evoked neuronal responses along the ascending auditory pathways from peripheral hearing end organs to the brain region53. Presence or absence of a response to acoustic stimuli of different frequencies and intensities allows the determination of AEP thresholds. The experimental setup was similar to that used by Parmentier et al. (2009)54 and Colleye et al. (2016)55.
No anaesthetic was used to restrain the fish during the AEP recordings. However, each fish was immobilized in a custom-made harness in order to prevent body movements while allowing normal respiration. The harness was closed dorsally and caudally with clamps attached to a steel frame. Three subdermal stainless steel needle electrodes (Rochester Electro-Medical, Lutz, FL, USA) were used to record electric signals. The recording electrode was inserted approximately 1 mm into the head, over the otic region. The reference electrode was placed into the fish’s epaxial musculature, whereas the ground electrode was in the water in close vicinity to the fish. Fish were suspended 10 cm below the water surface in a steel tube (1.15 m high, 22 cm diameter, 0.7 cm thickness) closed at the bottom with a square steel plate (40 × 40 cm). The tube was oriented vertically and filled with freshwater of approximately 26 °C up to a height of 1.12 m. An underwater loudspeaker (UW-30, Lubell Labs, Columbus, OH, USA) was placed at the bottom of the steel tube. The entire setup was enclosed in a soundproof chamber.
Stimulus generation and AEP recordings
A Tucker-Davies Technologies (TDT, Alachua, FL, USA) AEP workstation was used to generate sound stimuli and record AEP waveforms. TDT SigGen software was used to create sound stimuli with an RP2.1 enhanced real-time processor, a PA5 programmable attenuator to control sound level, and a power amplifier before being sent to and emitted by the underwater speaker. Sound stimuli were tone bursts of 50 ms in duration gated with a Hanning window. The phase of the tone was alternated between presentations to minimize electrical artefacts from the recordings. Fifteen frequencies were presented to each fish: 50, 150, 300, 600, 900, 1200, 1500, 1800, 2100, 2400, 2700, 3000, 3300, 3600 and 4000 Hz. At each frequency, sound levels were presented up to 164 dB re 1 µPa and were attenuated in 6 dB steps until a threshold level was determined. Evoked potentials recorded by the electrode were amplified (TDT HS4-DB4 amplifier, 10,000 gain), connected to an RP2.1 enhanced real-time processor, routed into the computer and averaged by BioSig software. At each frequency and for each sound level, the signal was presented 500 times. Sound levels of the acoustic stimuli were calibrated with a Brüel and Kjær 8101 hydrophone (Nærum, Denmark; sensitivity -164 dB re 1 V/µPa; bandwidth 0.1 Hz to 200 kHz) placed in the steel tube at the previous position of the fish’s head. The hydrophone was connected to a calibrated Brüel and Kjær 2610 amplifier that gave the absolute pressure level of sound stimuli. Evoked responses were averaged and power spectra were calculated using a 4096-point Fast Fourier Transform (FFT). The spectra were analysed for the presence of peaks at twice the stimulus frequency with heights at least 3 dB above the background level. For each frequency, the lowest sound level at which such peaks were present was defined as the auditory threshold for that frequency. Dead specimens of the eight species were also tested to confirm that recorded AEP traces were not artefacts. No responses were recorded with dead fishes (Fig. 1).
In addition to the hearing curves of each species, we also traced the hearing curves of maximum and minimum sensitivity for herbivorous (Pi. brachypomus, M. lippincottianus, M. rubripinnis and M. schomburgkii) and carnivorous species (S. elongatus, S. spilopleura, Py. nattereri and Py. piraya), as well as for vocal (Pi. brachypomus, S. elongatus, S. spilopleura, Py. nattereri and Py. piraya) and non-vocal species (M. lippincottianus, M. rubripinnis and M. schomburgkii). To achieve this, we selected the highest and lowest hearing thresholds among the species of each group (herbivorous vs. carnivorous, vocal vs. non-vocal) at each frequency tested.
The morphology of the auditory system of three Pygocentrus nattereri (120 mm, 134 mm and 155 mm in SL), three Piaractus brachypomus (131 mm, 139 mm and 168 mm in SL), two Myloplus rubripinnis (136 mm and 140 mm in SL), two Myleus schomburgkii (242 mm and 252 mm in SL), four Serrasalmus elongatus (63 mm, 88 mm, 119 mm and 152 mm in SL), and four Metynnis lippincottianus (96 mm, 102 mm, 109 mm and 112 mm in SL) was investigated using computed tomography (CT). These specimens were scanned at the National Museum of Natural History in Paris with a µCT scanner (v|tome|x 240 L, GE Sensing & Inspection Technologies phoenix|x-ray). The imaging system was set at 70 kV and specimens were scanned at an isotropic voxel size between 37.1 and 99.9 µm. Volume and surface rendering was performed with AMIRA 6.3 and AVIZO (VSG, Fei Company). Morphological measurements were performed with AVIZO. For each specimen, we measured the volume of the three Weberian ossicles having an auditory function (tripus, intercalarium and scaphium), the three otoliths (lapillus, sagitta and asteriscus) and the anterior part of the swimbladder. We also measured the surface area of each otolith as well as the length of the sagitta. In addition, the ratios of the volume of each Weberian ossicle to the total Weberian ossicle volume were calculated. The ratios of the volume (and surface) of each otolith to the total otolith volume (and total otolith surface) were also calculated, as well as the ratio of the volume of the anterior part of the swimbladder to the total swimbladder volume. Finally, we determined the ratio of the sagitta length to the fish standard length.
All procedures and all methods were approved by the ethical commission of the University of Liège (ethics case 1532). All experiments were performed in accordance with the relevant guidelines and regulations.
The variables were tested for the assumption of normality using Kolmogorov-Smirnov tests. A nested ANOVA was performed to compare sound pressure thresholds (dependent variable) obtained at the different frequencies tested. Species and frequency were selected as fixed factors. Tukey’s HSD post hoc tests were performed to compare sound pressure thresholds between species at each frequency.
Linear regressions were used to examine the relationship between fish size and auditory sensitivity at the different frequencies and also to determine if there was a relationship between the averaged morphological measurements of the different auditory structures and auditory sensitivity at the different frequencies. We also looked for trends between morphological features and auditory sensitivity at three larger frequency bands (50–1200 Hz, 1500–2400 Hz and 2700–3600 Hz).
Statistical analyses were performed with Statistica 13 and GraphPad Prism 5.0. Significance level was determined at P < 0.05.
The datasets generated and analysed during the current study are available from the corresponding author on reasonable request.
Slabbekoorn, H. et al. A noisy spring: The impact of globally rising underwater sound levels on fish. Trends Ecol. Evolut. 25, 419–427 (2010).
Ladich, F. Acoustic communication and the evolution of hearing in fishes. Philos. Trans. R. Soc. London (Biol.) 355, 1285–1288 (2000).
Vasconcelos, R. O., Fonseca, P. J., Amorim, M. C. P. & Ladich, F. Representation of complex vocalizations in the Lusitanian toadfish auditory system: Evidence of fine temporal, frequency and amplitude discrimination. Proc. R. Soc. Lond. (Biol.) 278, 826–834 (2011).
Remage-Healey, L., Nowacek, D. P. & Bass, A. H. Dolphin foraging sounds suppress calling and elevate stress hormone levels in a prey species, the Gulf toadfish. J. Exp. Biol. 209, 4444–4451, https://doi.org/10.1242/jeb.02525 (2006).
Fay, R. Soundscapes and the sense of hearing of fishes. Integr. Zool. 4, 26–32 (2009).
Parmentier, E. et al. The influence of various reef sounds on coral-fish larvae behaviour. J. Fish Biol. 86, 1507–1518, https://doi.org/10.1111/jfb.12651 (2015).
Simpson, S. D., Meekan, M. G., McCauley, R. D. & Jeffs, A. Attraction of settlement-stage coral reef fishes to reef noise. Mar. Ecol. Prog. Ser. 276, 263–268 (2004).
Ladich, F. Fish bioacoustics. Curr. Opin. Neurobiol. 28, 121–127 (2014).
Weber, E. H. De Aure et Auditu Hominis et Animalium. Pars I. De Aure Animalium Aquatilium. Leipzig; Gerhard Fleischer (1820).
Grande, T. & Young, B. The ontogeny and homology of the Weberian apparatus in the zebrafish Danio rerio (Ostariophysi: Cypriniformes). Zool. J. Linnean Soc. 140, 241–254 (2004).
Diogo, R. Origin, evolution and homologies of the Weberian apparatus: A new insight (Origen, evolución y homologías del aparato Weberiano: Un nuevo acercamiento). Int. J. Morphol. 27, 333–354 (2009).
Chardon, M. & Vandewalle, P. Evolutionary trends and possible origin of the Weberian apparatus. Neth. J. Zool. 47, 383–403 (1997).
Chardon, M., Parmentier, E. & Vandewalle, P. In Catfishes (eds G. Arratia, B. G. Kapoor, M. Chardon, & R. Diogo) 71–120, Science Publishers (2003).
Alexander, R. M. The structure of the Weberian apparatus in the Cyprini. Proc. Zool. Soc. Lond. 139, 451–473, https://doi.org/10.1111/j.1469-7998.1962.tb01839.x (1962).
von Frisch, K. The sense of hearing in fish. Nature 141, 8–11 (1938).
De Pinna, M. & Grande, T. Ontogeny of the Accessory Neural Arch in Pristigasteroid Clupeomorphs and Its Bearing on the Homology of the Otophysan Claustrum (Teleostei). Copeia, 838–845 (2003).
Grande, T. & de Pinna, M. in Mesozoic Fishes 3 - Systematics, Paleoenvironments and Biodiversity (eds G. Arratia & H-P. Schultze) 429–448 (2004).
Finneran, J. J. & Hastings, M. C. A mathematical analysis of the peripheral auditory system mechanics in the goldfish (Carassius auratus). J. Acoust. Soc. Am. 108, 1308–1321, https://doi.org/10.1121/1.1286099 (2000).
Popper, A. N. & Fay, R. R. Rethinking sound detection by fishes. Hear. Res. 273, 25–36 (2011).
Higgs, D. M., Rollo, A. K., Souza, M. J. & Popper, A. N. Development of form and function in peripheral auditory structures of the zebrafish (Danio rerio). J.. Acoust. Soc. Am. 113, 1145–1154 (2003).
Lechner, W., Heiss, E., Schwaha, T., Glösmann, M. & Ladich, F. Ontogenetic development of weberian ossicles and hearing abilities in the african bullhead catfish. PLoS ONE 6 (2011).
Ladich, F. & Wysocki, L. E. How does tripus extirpation affect auditory sensitivity in goldfish? Hear. Res. 182, 119–129 (2003).
Yan, H. Y., Fine, M. L., Horn, N. S. & Colón, W. E. Variability in the role of the gasbladder in fish audition. J. Comp. Physiol. (A) 186, 435–445 (2000).
Lechner, W. & Ladich, F. Size matters: Diversity in swimbladders and Weberian ossicles affects hearing in catfishes. J. Exp. Biol. 211, 1681–1689 (2008).
Planquette, P., Keith, P. & Le Bail, P.-Y. Atlas des poissons d’eau douce de Guyane. Tome 1., Publications scientifiques du Muséum national d’Histoire Naturelle (1996).
Anderson, J. T., Rojas, S. J. & Flecker, A. S. High-quality seed dispersal by fruit-eating fishes in Amazonian floodplain habitats. Oecol. 161, 279–290 (2009).
Lucas, C. M. Within flood season variation in fruit consumption and seed dispersal by two characin fishes of the Amazon. Biotropica 40, 581–589 (2008).
Ortí, G., Sivasundar, A., Dietz, K. & Jégu, M. Phylogeny of the Serrasalmidae (Characiformes) based on mitochondrial DNA sequences. Genet. Mol. Biol. 31, 343–351 (2008).
Thompson, A. W., Betancur-R, R., Lopez-Fernandez, H. & Orti, G. A time-calibrated, multi-locus phylogeny of piranhas and pacus (Characiformes: Serrasalmidae) and a comparison of species tree methods. Mol. Phylogenet. Evol. 81, 242–257 (2014).
Millot, S., Vandewalle, P. & Parmentier, E. Sound production in red-bellied piranhas (Pygocentrus nattereri, Kner): An acoustical, behavioural and morphofunctional study. J. Exp. Biol. 214, 3613–3618 (2011).
Markl, H. Sound production in piranhas (Serrasalminae, Characidae). Z. vergl. Physiologie 74, 39–56 (1971).
Mélotte, G., Vigouroux, R., Michel, C. & Parmentier, E. Interspecific variation of warning calls in piranhas: A comparative analysis. Sci. Rep. 6, https://doi.org/10.1038/srep36127 (2016).
Popper, A. N., Ramcharitar, J. & Campana, S. E. Why otoliths? Insights from inner ear physiology and fisheries biology. Mar. Freshwater Res. 56, 497–504 (2005).
Higgs, D. M., Souza, M. J., Wilkins, H. R., Presson, J. C. & Popper, A. N. Age- and size-related changes in the inner ear and hearing ability of the adult zebrafish (Danio rerio). JARO - J. Assoc. Res. Otolaryngol. 3, 174–184 (2001).
Stabentheiner, A. Correlations between hearing and sound production in piranhas. J. Comp. Physiol. (A) 162, 67–76 (1988).
Ladich, F. Did auditory sensitivity and vocalization evolve independently in otophysan fishes? Brain Behav. Evol. 53, 288–304 (1999).
Wysocki, L. E. & Ladich, F. Can fishes resolve temporal characteristics of sounds? New insights using auditory brainstem responses. Hear. Res. 169, 36–46 (2002).
Ladich, F. & Popper, A. N. Comparison of the inner ear ultrastructure between teleost fishes using different channels for communication. Hear. Res. 154, 62–72, https://doi.org/10.1016/S0378-5955(01)00217-9 (2001).
Markl, H. Aggression and prey capture in piranhas (Serrasalminae, Characidae). Z. Tierpsychol. 30, 190–216 (1972).
Andersen, R. A. & Enger, P. S. Microphonic potentials from the sacculus of a teleost fish. Comp. Biochem. Physiol. 27, 879–881 (1968).
Enger, P. S., Hawkins, A. D., Sand, O. & Chapman, C. J. Directional sensitivity of saccular microphonic potentials in the haddock. J. Exp. Biol. 59, 425–433 (1973).
Fay, R. R. & Edds-Walton, P. L. Diversity in frequency response properties of saccular afferents of the toadfish. Opsanus tau. Hear. Res. 113, 235–246, https://doi.org/10.1016/S0378-5955(97)00148-2 (1997).
Popper, A. N. & Schilt, C. R. In Fish Bioacoustics Vol. 32 (eds J. Webb, R. Fay, & A. Popper) 17–48, Springer Handbook of Auditory Research (2008).
Schulz-Mirbach, T., Ladich, F., Plath, M., Metscher, B. D. & Heß, M. Are accessory hearing structures linked to inner ear morphology? Insights from 3D orientation patterns of ciliary bundles in three cichlid species. Front. Zool. 11 (2014).
Bird, N. C. & Hernandez, L. P. Morphological variation in the Weberian apparatus of cypriniformes. J. Morphol. 268, 739–757 (2007).
Watson, J. M. The development of the Weberian ossicles and anterior vertebrae in the goldfish. Proc. R. Soc. Lond. (Biol.) 127, 452–472 (1939).
Radermaker, F., Surlemont, C., Sanna, P., Chardon, M. & Vandewalle, P. Ontogeny of the Weberian apparatus of Clarias gariepinus (Pisces Siluriformes). Can. J. Zool. 67, 2090–2097 (1989).
Popper, A. N. The effects of size on auditory capacities of the goldfish. J. Aud. Res. 11, 239–247 (1971).
Jégu, M., Keith, P. & Belmonte-Jégu, E. A new species of Tometes (Teleostei: Characidae: Serrasalminae) from the Guianian shield, Tometes lebaili n. sp. BFPP - Bull. Fr. Peche Prot. Milieux Aquat., 23–48 (2002).
Jégu, M., Dos Santos, G. M., Keith, P. & Le Bail, P. Y. Supplementary description and rehabilitation of Tometes trilobatus Valenciennes, 1850, type-species of Tometes Valenciennes (Characidae: Serrasalminae). Cybium 26, 99–122 (2002).
Lugli, M. The tradeoff between signal detection and recognition rules auditory sensitivity under variable background noise conditions. J. Theor. Biol. 386, 1–6, https://doi.org/10.1016/j.jtbi.2015.08.033 (2015).
Kenyon, T. N., Ladich, F. & Yan, H. Y. A comparative study of hearing ability in fishes: The auditory brainstem response approach. J. Comp. Physiol. (A) 182, 307–318 (1998).
Corwin, J. T., Bullock, T. H. & Schweitzer, J. The auditory brain stem response in five vertebrate classes. Electroencephalogr. Clin. Neurophysiol. 54, 629–641, https://doi.org/10.1016/0013-4694(82)90117-1 (1982).
Parmentier, E., Colleye, O. & Mann, D. Hearing ability in three clownfish species. J. Exp. Biol. 212, 2023–2026 (2009).
Colleye, O., Kéver, L., Lecchini, D., Berten, L. & Parmentier, E. Auditory evoked potential audiograms in post-settlement stage individuals of coral reef fishes. J. Exp. Mar. Biol. Ecol. 483, 1–9 (2016).
We thank Zora Gabsi, Philippe Keith, and Patrice Pruvost (MNHN, CNRS UMR 7208) for assistance and access to MNHN specimen loans. We are grateful to Miguel Garcia Sanz and Patricia Wils from the AST-RX platform at MNHN (CNRS UMS 2700) for μCT scanning and training in Avizo. This study was supported by grants from F.R.S.-FNRS (no. T.0101.15). K. B. was funded by a Marie-Skłodowska Curie fellowship (EU project 625039 – EvoMorphASIS). G.M. was funded by the Fonds pour la formation à la Recherche dans l’Industrie et l’Agriculture (F.R.S.-FNRS).
The authors declare that they have no competing interests.
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Mélotte, G., Parmentier, E., Michel, C. et al. Hearing capacities and morphology of the auditory system in Serrasalmidae (Teleostei: Otophysi). Sci Rep 8, 1281 (2018). https://doi.org/10.1038/s41598-018-19812-1
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