An Intermediate in the evolution of superfast sonic muscles
- Hin-Kiu Mok†1,
- Eric Parmentier†2,
- Kuo-Hsun Chiu1, 3,
- Kai-En Tsai1,
- Pai-Ho Chiu1 and
- Michael L Fine4Email author
© Mok et al; licensee BioMed Central Ltd. 2011
Received: 4 October 2011
Accepted: 29 November 2011
Published: 29 November 2011
Intermediate forms in the evolution of new adaptations such as transitions from water to land and the evolution of flight are often poorly understood. Similarly, the evolution of superfast sonic muscles in fishes, often considered the fastest muscles in vertebrates, has been a mystery because slow bladder movement does not generate sound. Slow muscles that stretch the swimbladder and then produce sound during recoil have recently been discovered in ophidiiform fishes. Here we describe the disturbance call (produced when fish are held) and sonic mechanism in an unrelated perciform pearl perch (Glaucosomatidae) that represents an intermediate condition in the evolution of super-fast sonic muscles.
The pearl perch disturbance call is a two-part sound produced by a fast sonic muscle that rapidly stretches the bladder and an antagonistic tendon-smooth muscle combination (part 1) causing the tendon and bladder to snap back (part 2) generating a higher-frequency and greater-amplitude pulse. The smooth muscle is confirmed by electron microscopy and protein analysis. To our knowledge smooth muscle attachment to a tendon is unknown in animals.
The pearl perch, an advanced perciform teleost unrelated to ophidiiform fishes, uses a slow type mechanism to produce the major portion of the sound pulse during recoil, but the swimbladder is stretched by a fast muscle. Similarities between the two unrelated lineages, suggest independent and convergent evolution of sonic muscles and indicate intermediate forms in the evolution of superfast muscles.
Although neural circuitry for vocalization shares similarities between some fishes and tetrapods , little is known about the evolution of fish sonic mechanisms. Rather than a homologous syrinx or larynx, fish sounds are produced by an extraordinary diversity of mechanisms utilizing super-fast muscles that appear to evolve convergently [2, 3]. In common between fishes and tetrapods, muscles act on organs derived from endodermal structures: swimbladder in fishes and trachea in tetrapods. Sonic swimbladder muscles can be extrinsic or intrinsic. Extrinsic muscles typically originate on the skull and insert on the swimbladder or a bony structure attached to the bladder. Intrinsic muscles, the less common condition, attach exclusively to the swimbladder wall and tend to be associated with prolonged tonal sounds [4–6].
Muscles can change insertions over evolutionary time , but how the process would start is unclear. Head muscles have migrated to the swimbladder multiple times, and all known examples are sonic except in the lion fish in which the muscle appears to manipulate the bladder for posture control . Based on embryology  and parsimony, Fine and Ladich  speculated that extrinsic muscles preceded intrinsic ones because it would be simpler to move the insertion of an existing muscle to the swimbladder than to create a muscle de novo. In support of this idea, intrinsic sonic muscles and the sonic nerves in toadfish form in the occipital spinal cord, migrate and attach to the swimbladder .
Fish swimbladder muscles are often considered the fastest muscles in vertebrates . Sound from fast sonic systems is produced as a forced rather than a resonant response, i.e. muscle cycle time (contraction and relaxation) and not the natural frequency of the swimbladder cavity, determines sound fundamental frequency [4, 12, 13]. For instance, the oyster toadfish routinely contracts its muscles at 200 Hz to produce a courtship call with that fundamental frequency and can follow an electrical stimulus at 400 Hz without tetanizing . However, slow bladder movement does not generate audible sound [12, 14]. Therefore, the evolution of superfast muscles has been a mystery since there was no clear role for slow muscles, and intermediates were lacking.
Recently, slow sonic swimbladder muscles have been discovered in carapids  and appear to occur in various ophidiiform fishes [16–20]; these muscles tetanize around 10 Hz . The carapid swimbladder contains a thin fenestra near its anterior pole, which stretches during contraction of the slow sonic muscle. The contraction pulls the anterior swimbladder forward until it snaps back exciting sound production. Ophidion rochei has more complex sonic system with a bean-shaped rocker bone protruding from the forward wall of the bladder that is rotated in opposite directions by antagonistic pairs of sonic muscle . Its sound pulses consist of two parts, potentially corresponding to opposite motions of the rocker bone. Consistent with slow muscles, the muscle contraction rate generates the number of sound pulses (one pulse per contraction) but not the frequency spectrum of the pulses as in fast muscles.
The pearl perch Glaucosoma buergeri Richardson is an advanced perciform teleost unrelated to ophidiiform fishes and possesses swimbladder muscles suggestive of sound production . Its sonic anatomy is complex and mirrors many aspects of ophidiids, suggesting the presence of slow muscles. In this study we investigate the anatomy of sound production including ultrastructure of sonic muscles and electrophoresis of muscle proteins, describe sound properties and relate them to sonic anatomy, and posit an evolutionary scheme that for the first time allows for intermediates in the evolution of super-fast sonic muscles.
Materials and methods
Pearl perch were caught between about 60 and 150 m of water on the bottom by hook and line about 100 km from Kaohsiung Harbor, Taiwan. Despite decompression, most fish were capable of producing sounds, indicating intact swimbladders. We evoked disturbance sounds in 6 fish (430 to 550 mm standard length) in a polystyrene tank (52 × 30 cm: water depth 20 cm) by gently touching the fish's abdomen. Sounds were recorded with a hydrophone (HP-A1 Burns Electronics) on to a Sony linear PCM-M10 recorder and analyzed with Avisoft (at least eight sounds per fish). Protocols were approved by the National Sun Yan-sen University Animal Care and Use Committee.
Animals were returned to the lab for dissection, histology and electrophoresis. Histology on the internal muscle fixed in 7% paraformaldehyde in phosphate buffer suggested it was a smooth muscle, and therefore electron microscopy was performed on another individual. Several small samples of sonic and epaxial muscles were fixed in 2.5% glutaraldehyde. Morphology was first observed in 6-7 μm sections stained with toluidin blue and then ultrathin sections were stained with uranyl acetate and lead citrate and examined with a JEOL JEM 11SX electron microscope.
We utilized (1) SDS-PAGE analysis combined with LC-MS/MS to probe the muscles for alpha transgellin, a smooth-muscle specific protein and (2) Western blotting for troponin T, a marker present in striated but not smooth muscle, and alpha (sarcomeric) actin.
Approximately 0.1 g of the two sonic muscles, white trunk muscle and the swim bladder were individually homogenized with a Pro200 homogenizer (Pro Scientific Inc. Oxford, CT USA) in 0.07 M sodium phosphate buffer (pH 7.4) and centrifuged at 4°C for 20 min at 16000 g to remove the cell debris. Supernatant protein concentration was determined with the Bradford protein assay reagent (Bio-rad). Proteins were resolved by SDS-polyacrylamide gel electrophoresis (PAGE) performed on a 12% gel, and bands were visualized with silver staining. Specific bands were excised for identification, washed three times with 25 mM ammonium bicarbonate in water and 50% (v/v) acetonitrile (ACN) in 25 mM ammonium bicarbonate. Protein reduction was subsequently performed by incubating in 0.5 M dithiothrietol (DTT) for 1 h at 56 °C and then alkylating with 50 μL saturated iodoacetamide (IAA) for 45 min at room temperature in the dark. The gel sample was digested with 20 μg of sequencing-grade modified trypsin (Promega) with a sufficient volume of 25 mM ammonium bicarbonate to completely saturate the gel. The sample was incubated at 37 °C for an overnight digestion. Supernatants containing the peptides were transferred to siliconized 0.5 mL Eppendorf tubes. Remaining peptides in the gel pieces were extracted by incubation with 20 μL of 50% (v/v) ACN containing 5% (v/v) formic acid for 20 min. Extracted peptides were combined with those in the Eppendorf tubes, and nano-HPLC-MS/MS analysis was performed to identify tryptic peptides.
Extracted peptides were transferred to vials, and 8 μL of sample was fractionated by capillary reverse-phase liquid chromatography on a C18 microcapillary column (75 μm i.d. × 15 cm) coupled with an ion trap mass spectrometer (LCQ DECA XP Plus, ThermoFinnigan, San Jose, CA). The mobile phases were 0.1% (v/v) formic acid in H2O (buffer A) and 0.1% (v/v) formic acid in acetonitrile (buffer B). The gradient profile consisted of a linear 0% to 5% buffer B at 2 min and then progressed to 5% buffer B at 2 min and to 60% at 40 min. The samples were introduced into the mass spectrometer through an electrospray source with the application of a distal 1.6-1.7 kV spraying voltage, and the scan range of each full MS scan m/z 450-2000.
The proteins identified by MS/MS fragmentation spectra were searched against the NCBI Actinopterygii (ray-finned fishes) sequence database (version 20090616; 148434 sequences) with the MASCOT algorithm (v2.1.0, Matrix Science, London, UK). The mass search parameters were set: peptide mass tolerance, 1 Da; MS/MS tolerance, 1 Da; peptide charge, +1,+2, and +3; data format, sequence (DTA); Instrument, ESI-TRAP.; missed cleavage, 2; consideration for fixed modifications such as carbamidomethyl, and for variable modifications as deamidated and oxidation.
Western blotting was used to verify the expression of selected proteins including troponin T and sarcomeric actin. Ten μg of protein from the various muscles and the swim bladder were mixed with SDS sample buffer and heated at 95°C for 5 min. Proteins were separated on a 12% SDS-PAGE and transferred to PVDF membranes (Millipore). The swimbladder was used as negative control. The membranes were blocked in a 5% nonfat milk solution for 1 h at room temperature and then probed with antibodies against troponin T (1:200 dilution, Santa Cruz Biotechnology) and against a monoclonal antibody to alpha sarcomeric actin (1:1,000 dilution, Abcam). The membranes were washed 3× with tris-buffered saline containing tween-20 (TBST) and incubated with secondary antibody in TBST/2% skim milk. Bound antibody was detected with the Enhanced Chemiluminescence System. Chemiluminescent signals were captured with the Fujifilm LAS 3000 system (Fujifilm). Duplicate experiments were performed at least 3×.
Because the swimbladder did not contain muscle actin, 10 μg of each sample examined by Western blotting were separated and visualized by silver staining to verify the protein integrity of each sample.
Paired red anterior sonic muscles originate on the base of the pterotic bones on the skull and insert on the outside of the dorsal bladder at the forward edge of the fenestra (Figure 1). A tendon from the 9th vertebra ends in a single red-colored muscle that inserts on the tunica externa on the inner side of the lumen of the anterior swimbladder. Therefore, the anterior striated muscle and posterior muscle-tendon spring apparatus attach to opposite sides of the bladder and appear to function as antagonists.
Pulling on the anterior sonic muscles extends the anterior bladder and fenestra forward and adds strain to the tendon-internal muscle combination, which pulls the bladder back upon relaxation of the anterior muscles. We therefore conclude that the weak PP1 is caused by contraction of a fast sonic muscle (the anterior striated muscles), and the higher frequency and greater amplitude of PP2 is caused by rapid rebound expected from a stretched tendon , as in slow sonic mechanisms.
The complex sonic anatomy of the pearl perch includes a number of structures that are uncommon in fishes . The involvement of the smooth muscle is extraordinary. To our knowledge smooth muscles are not known to attach to tendons. Smooth muscle does occur within swimbladder walls as a thin layer  corresponding to the muscularis mucosa of the digestive tract. The red smooth sonic muscle is organized to assume a function at least partially analogous to that of striated muscle. Its precise function is not clearly understood, but slow speed of contraction is unlikely to contribute to sound frequency or pulse generation. In the syrinx of male ducks, smooth muscle is not the source of sound but has been hypothesized to modulate sound by altering tension of the inner tympaniform membranes . Similarly smooth muscle contributes to a collagenous ring affecting gaze in primates . For the pearl perch we suggest a common mechanical analog of a spring (the tendon) and a dashpot (the smooth muscle), which would function to damp swimbladder vibrations permitting pauses within a relatively rapid series of pulses (Figure 4) . This hypothesis is supported by sounds we recorded from pempherids, a sister family to glaucosomatids. Pempherids have a tendon but no smooth muscle and produce longer duration pulses that continue to oscillate for more cycles before damping. The mechanics of contraction and rebound await study in these related families.
Although many but not most fishes have sonic swimbladder muscles , there is no known phylogenetic continuity as with the bird syrinx or mammalian larynx . In typical fast systems in fishes, sonic muscles deform the bladder at a rapid rate that determines fundamental frequency [4, 12, 13]. Slow systems however, typically depend on rebound of stretched swimbladders and tendons [15–20]: features include a free anterior region of the swimbladder that is stretched by anterior sonic muscles, a stretchable swimbladder fenestra, a relatively fixed posterior region that is anchored to the backbone, and a tendon or other means of storing strain energy that causes the bladder to snap back rapidly. The fast sonic muscles of the pearl perch produce a weak component of the sound waveform suggesting that acoustic communication at any distance would depend on the second part of the pulse. The finding in pearl perch of a hybrid system, i.e. a fast muscle in a sonic system with the parallels to slow muscles listed above indicates a transitional form in the evolution of superfast sonic muscles. Therefore, we suggest a series of stages in sonic-muscle evolution: 1) no sonic muscles, 2) slow muscles that work primarily with a bone or tendon and produce sound by rebound, 3) fast muscles that still utilize rebound (i.e. the pearl perch and related families) and 4) fast muscles (extrinsic and intrinsic) that drive the bladder directly to express the peak frequency of the sound. Because swimbladder muscles appear to have formed independently multiple times, we suggest these stages would not necessarily correlate with the phylogenetic position of the family so that a more derived family could be at an earlier stage in the progression.
The disturbance call of the pearl perch is composed of two parts. Although the swimbladder is stretched by a fast sonic muscle (part 1), the second and greater amplitude part of the call is produced by bladder recoil facilitated by strain energy in a tendon-smooth muscle pair. Rebound sounds are characteristic of slow sonic mechanisms in unrelated ophidiiform fishes. The pearl perch utilizing characteristics of slow and fast systems therefore represents in an intermediate condition in the evolution of superfast sonic muscles that drive swimbladder vibration directly.
Supported in part by National Science Council (ROC) grant NSC96-2621-B-110-003-MY3 to H.K.M. and FRFC n° 2.4.535.10.F from the F.R.S.-FNRS. R.C. Shiue helped with sound analyses, and the National Cheng-Kung University Proteomics Research Core Laboratory assisted in mass spectrometry analysis. N. Decloux (ULg) helped with electron microscopy and Yves-Eric Corbisier kindly realized the 3D movie. E.P. is Research Associate from the F.R.S.-FNRS (Belgium).
- Bass AH, Gilland EH, Baker R: Evolutionary Origins for Social Vocalization in a Vertebrate Hindbrain-Spinal Compartment. Science. 2008, 321: 417-421. 10.1126/science.1157632.PubMed CentralView ArticlePubMedGoogle Scholar
- Ladich F, Fine M: Sound-Generating Mechanisms in Fishes: A Unique Diversity in Vertebrates. Communication in Fishes. Edited by: Ladich F, Collin SP, Moller P, Kapoor BG. 2006, Endfield: Science Publishers, 1: 3-43.Google Scholar
- Parmentier E, Diogo R: Evolutionary trends of swimbladder sound mechanisms in some teleost fishes. Communication in Fishes. Edited by: Ladich F, Collin SP, Moller P, Kapoor BG. 2006, Enfield, NH, USA: Jersey Plymouth: Science Publishers, 43-68.Google Scholar
- Bass AH, McKibben JR: Neural mechanisms and behaviors for acoustic communication in teleost fish. Progress in Neurobiology. 2003, 69: 1-26. 10.1016/S0301-0082(03)00004-2.View ArticlePubMedGoogle Scholar
- Fine ML, Thorson RF: Use of Passive Acoustics for Assessing Behavioral Interactions in Individual Toadfish. Transactions of the American Fisheries Society. 2008, 137: 627-637. 10.1577/T04-134.1.View ArticleGoogle Scholar
- Tellechea JS, Norbis W, Olsson D, Fine ML: Calls of the black drum (Pogonias cromis: Sciaenidae): geographical differences in sound production between northern and southern hemisphere populations. Journal of Experimental Zoology Part A: Ecological Genetics and Physiology. 2011, 315A: 48-55. 10.1002/jez.651.View ArticleGoogle Scholar
- Diogo R, Abdala V: Muscles of vertebrates: comparative anatomy, evolution, homologies and development. 2010, Enfield: Science PublishersView ArticleGoogle Scholar
- Hornstra HM, Herrel A: Gas Bladder Movement in Lionfishes: A Novel Mechanism for Control of Pitch. Journal of Morphology. 2004, 260: 1-10.1002/jmor.10141.View ArticleGoogle Scholar
- Tracy HC: Stages in the development of the anatomy of motility of the toadfish (Opsanus tau). The Journal of Comparative Neurology. 1959, 111: 27-81. 10.1002/cne.901110103.View ArticleGoogle Scholar
- Fine ML, Ladich F: Sound production, spine locking and related adaptations. Catfishes. Edited by: Kapoor BG, Arratia G, Chardon M, Diogo R. 2003, Enfield: Science Publishers, 248-290.Google Scholar
- Tavolga WN: Sonic characteristics and mechanisms in marine fishes. Marine Bio-acoustics. Edited by: Tavolga WN. 1964, Oxford: Pergamon Press, 195-211.Google Scholar
- Fine ML, Malloy KL, King CB, Mitchell SL, Cameron TM: Movement and sound generation by toadfish swimbladder. Journal of comparative Physiology A. 2001, 187: 371-379. 10.1007/s003590100209.View ArticleGoogle Scholar
- Connaughton MA: Sound generation in the searobin (Prionotus carolinus), a fish with alternate sonic muscle contraction. J Exp Biol. 2004, 207: 1643-1654. 10.1242/jeb.00928.View ArticlePubMedGoogle Scholar
- Fine ML, King CB, Cameron TM: Acoustical properties of the swimbladder in the oyster toadfish Opsanus tau. Journal of Experimental Biology. 2009, 212: 3542-3552. 10.1242/jeb.033423.PubMed CentralView ArticlePubMedGoogle Scholar
- Parmentier E, Lagardere J-P, Braquegnier J-B, Vandewalle P, Fine ML: Sound production mechanism in carapid fish: first example with a slow sonic muscle. J Exp Biol. 2006, 209: 2952-2960. 10.1242/jeb.02350.View ArticlePubMedGoogle Scholar
- Mann D, Bowers-Altman J, Rountree RA: Sounds Produced by the Striped Cusk-Eel Ophidion marginatum (Ophidiidae) during Courtship and Spawning. Copeia. 1997, 1997: 3-View ArticleGoogle Scholar
- Parmentier E, Fontenelle N, Fine ML, Vandewalle P, Henrist C: Functional morphology of the sonic apparatus in Ophidion barbatum (Teleostei, Ophidiidae). Journal of Morphology. 2006, 267: 1461-1468. 10.1002/jmor.10496.View ArticlePubMedGoogle Scholar
- Fine ML, Lin H, Nguyen BB, Rountree RA, Cameron TM, Parmentier E: Functional morphology of the sonic apparatus in the fawn cusk-eel Lepophidium profundorum (Gill, 1863). Journal of Morphology. 2007, 268: 953-966. 10.1002/jmor.10551.View ArticlePubMedGoogle Scholar
- Nguyen TK, Lin H, Parmentier E, Fine ML: Seasonal variation in sonic muscles in the fawn cusk-eel Lepophidium profundorum. Biology Letters. 2008, 4: 707-710. 10.1098/rsbl.2008.0383.PubMed CentralView ArticlePubMedGoogle Scholar
- Parmentier E, Bouillac G, Dragičević B, Dulčić J, Fine M: Call properties and morphology of the sound-producing organ in Ophidion rochei (Ophidiidae). Journal of Experimental Biology. 2010, 213: 3230-3236. 10.1242/jeb.044701.View ArticlePubMedGoogle Scholar
- McKay RJ: FAO species catalogue. Vol. 17. Pearl perches of the world. (Family Glaucosomatidae). An annotated and illustrated catalogue of the pearl perches known to date. FAO Fisheries Synopsis. 1997, 125: 26-Google Scholar
- Feher J, Waybright T, Fine M: Comparison of sarcoplasmic reticulum capabilities in toadfish sonic muscle and rat fast twitch muscle. Journal of Muscle Research and Cell Motility. 1998, 19: 661-674. 10.1023/A:1005333215172.View ArticlePubMedGoogle Scholar
- Mitchell S, Poland J, Fine ML: Does muscle fatigue limit advertisement calling in the oyster toadfish Opsanus tau?. Animal Behaviour. 2008, 76: 1011-1016. 10.1016/j.anbehav.2008.03.024.View ArticleGoogle Scholar
- McNeill Alexander R: Tendon elasticity and muscle function. Comparative Biochemistry and Physiology - Part A: Molecular & Integrative Physiology. 2002, 133: 1001-1011. 10.1016/S1095-6433(02)00143-5.View ArticleGoogle Scholar
- Smith FM, Croll RP: Autonomic control of the swimbladder. Autonomic Neuroscience. 2011, 165: 140-148. 10.1016/j.autneu.2010.08.002.View ArticlePubMedGoogle Scholar
- Frank T, Walter I, Probst A, König HE: Histological Aspects of the Syrinx of the Male Mallard (Anas platyrhynchos). Anatomia, Histologia, Embryologia. 2006, 35: 396-401. 10.1111/j.1439-0264.2006.00701.x.View ArticlePubMedGoogle Scholar
- Demer J, Oh SY, Clark RA, Poukens V: Evidence for a pulley of the inferior oblique muscle. Investiative Opthamology & Visual Science. 2003, 44: 3856-3865.View ArticleGoogle Scholar
- Steidel RF, (Ed): An introduction to mechanical vibration. 1989, New York: WileyGoogle Scholar
- Lobel PS, Kaatz I, Rice AN: Acoustical behavior of reef Fishes. Reproduction and sexuality in marine fishes: patterns and processes. Edited by: Cole KS. 2010, Berkeley: University of California Press, 307-387.Google Scholar
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