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Gymnotiformes

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South American knifefish
Temporal range: Late Jurassic –Recent [1]
Black ghost knifefish, Apteronotus albifrons
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Actinopterygii
(unranked): Otophysi
Order: Gymnotiformes
Type species
Gymnotus carapo
Despite the name, the electric eel is a type of knifefish.

The Gymnotiformes /dʒɪmˈnɒtɪfɔːrmiːz/ are an order of teleost bony fishes commonly known as Neotropical knifefish or South American knifefish. They have long bodies and swim using undulations of their elongated anal fin. Found almost exclusively in fresh water (the only exceptions are species that occasionally may visit brackish water to feed), these mostly nocturnal fish are capable of producing electric fields to detect prey, for navigation, communication, and, in the case of the electric eel (Electrophorus electricus), attack and defense.[2] A few species are familiar to the aquarium trade, such as the black ghost knifefish (Apteronotus albifrons), the glass knifefish (Eigenmannia virescens), and the banded knifefish (Gymnotus carapo).

Description

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Anatomy and locomotion

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Aside from the electric eel (Electrophorus electricus), Gymnotiformes are slender fish with narrow bodies and tapering tails, hence the common name of "knifefishes". They have neither pelvic fins nor dorsal fins, but do possess greatly elongated anal fins that stretch along almost the entire underside of their bodies. The fish swim by rippling this fin, keeping their bodies rigid. This means of propulsion allows them to move backwards as easily as they move forward.[3]

The knifefish has approximately one hundred and fifty fin rays along its ribbon-fin. These individual fin rays can be curved nearly twice the maximum recorded curvature for ray-finned fish fin rays during locomotion. These fin rays are curved into the direction of motion, indicating that the knifefish has active control of the fin ray curvature, and that this curvature is not the result of passive bending due to fluid loading.[4]

Different wave patterns produced along the length of the elongated anal fin allow for various forms of thrust. The wave motion of the fin resembles traveling sinusoidal waves. A forward traveling wave can be associated with forward motion, while a wave in the reverse direction produces thrust in the opposite direction.[5] This undulating motion of the fin produced a system of linked vortex tubes that were produced along the bottom edge of the fin. A jet was produced at an angle to the fin that was directly related to the vortex tubes, and this jet provides propulsion that moves the fish forward.[6] The wave motion of the fin is similar to that of other marine creatures, such as the undulation of the body of an eel, however the wake vortex produced by the knifefish was found to be a reverse Kármán vortex. This type of vortex is also produced by some fish, such as trout, through the oscillations of their caudal fins.[7] The speed at which the fish moved through the water had no correlation to the amplitude of its undulations, however it was directly related to the frequency of the waves generated.[8]

Studies have shown that the natural angle between the body of the knifefish and its fin is essential for efficient forward motion, for if the anal fin was located directly underneath, then an upwards force would be generated with forward thrust, which would require an additional downwards force in order to maintain neutral buoyancy.[7] A combination of forward and reverse wave patterns, which meet towards the center of the anal fin, produce a heave force allowing for hovering, or upwards movement.[5]

The ghost knifefish can vary the undulation of the waves, as well as the angle of attack of the fin to achieve various directional changes. The pectoral fins of these fishes can help to control roll and pitch control.[9] By rolling they can generate a vertical thrust to quickly, and efficiently, ambush their prey.[7] The forward movement is determined exclusively by the ribbon fins and the contribution of the pectoral fins for forward movement was negligible.[10] The body is kept relatively rigid and there is very little motion of the center of mass motion during locomotion compared to the body size of the fish.[8]

The caudal fin is absent, or in the apteronotids, greatly reduced. The gill opening is restricted. The anal opening is under the head or the pectoral fins.[11]

Electroreception and electrogenesis

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Further information: Electroreception and electrogenesis

These fish possess electric organs that allow them to produce electric fields, which are usually weak. In most gymnotiforms, the electric organs are derived from muscle cells. However, adult apteronotids are one exception, as theirs are derived from nerve cells (spinal electromotor neurons). In gymnotiforms, the electric organ discharge may be continuous or pulsed. If continuous, it is generated day and night throughout the entire life of the individual. Certain aspects of the electric signal are unique to each species, especially a combination of the pulse waveform, duration, amplitude, phase and frequency.[12]

The electric organs of most Gymnotiformes produce tiny discharges of just a few millivolts, far too weak to cause any harm to other fish. Instead, they are used to help navigate the environment, including locating the bottom-dwelling invertebrates that compose their diets.[13] They may also be used to send signals between fish of the same species.[14] In addition to this low-level field, the electric eel also has the capability to produce much more powerful discharges to stun prey.[3]

Taxonomy

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There are currently about 250 valid gymnotiform species in 34 genera and five families, with many additional species yet to be formally described.[15][16][17] The actual number of species in the wild is unknown.[18] Gymnotiformes is thought to be the sister group to the Siluriformes[19][20] from which they diverged in the Cretaceous period (about 120 million years ago). The families have traditionally been classified over suborders and superfamilies as below.[21][17]

Order Gymnotiformes

Suborder Gymnotoidei
Family Gymnotidae (banded knifefishes and electric eels)
Suborder Sternopygoidei
Superfamily Rhamphichthyoidea
Family Rhamphichthyidae (sand knifefishes)
Family Hypopomidae (bluntnose knifefishes)
Superfamily Apteronotoidea
Family Sternopygidae (glass and rat-tail knifefishes)
Family Apteronotidae (ghost knifefishes)

Phylogeny

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Most gymnotiforms are weakly electric, capable of active electrolocation but not of delivering shocks. The electric eels, genus Electrophorus, are strongly electric, and are not closely related to the Anguilliformes, the true eels.[22] Their relationships were analysed by sequencing their mitochondrial genomes in 2019. This shows that contrary to earlier ideas, the Apteronotidae and Sternopygidae are not sister taxa, and that the Gymnotidae are deeply nested among the other families.[23]

Actively electrolocating fish are marked on the phylogenetic tree with a small yellow lightning flash . Fish able to deliver electric shocks are marked with a red lightning flash . There are other electric fishes in other families (not shown).[13][24][25]

Otophysi

Siluriformes (catfish) (some )

Gymnotiformes

Apteronotidae (ghost knifefishes)

Rhamphichthyoidea

Hypopomidae (bluntnose knifefishes)

Rhamphichthyidae (sand knifefishes)

Gymnotidae

Gymnotus (banded knifefishes)

Electrophorus (electric eels)

Sternopygidae (glass knifefishes)

Characoidei (piranhas, tetras, and allies)

Distribution and habitat

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Gymnotiform fishes inhabit freshwater rivers and streams throughout the humid Neotropics, ranging from southern Mexico to northern Argentina. They are nocturnal fishes. The families Gymnotidae and Hypopomidae are most diverse (numbers of species) and abundant (numbers of individuals) in small non-floodplain streams and rivers, and in floodplain "floating meadows" of aquatic macrophytes (e.g., Eichornium, the Amazonian water hyacinth). On the other hand, families Apteronotidae and Sternopygidae are most diverse and abundant in large rivers. Species of Rhamphichthyidae are moderately diverse in all these habitat types.

Evolution

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Further information: Electric fish

Gymnotiformes are among the more derived members of Ostariophysi, a lineage of primary freshwater fishes. The only known fossils are from the Miocene about 7 million years ago (Mya) of Bolivia.[26]

Gymnotiformes has no extant species in Africa. This may be because they did not spread into Africa before South America and Africa split, or it may be that they were out-competed by Mormyridae, which are similar in that they also use electrolocation.[15]

Approximately 150 Mya, the ancestor to modern-day Gymnotiformes and Siluriformes were estimated to have convergently evolved ampullary receptors, allowing for passive electroreceptive capabilities.[27] As this characteristic occurred after the prior loss of electroreception among the subclass Neopterygii[28] after having been present in the common ancestor of vertebrates, the ampullary receptors of Gymnotiformes are not homologous with those of other jawed non-teleost species, such as chondricthyans.[29]

Gymnotiformes and Mormyridae have developed their electric organs and electrosensory systems (ESSs) through convergent evolution.[30] As Arnegard et al. (2005) and Albert and Crampton (2005) show,[31][32] their last common ancestor was roughly 140 to 208 Mya, and at this time they did not possess ESSs. Each species of Mormyrus (family: Mormyridae) and Gymnotus (family: Gymnotidae) have evolved a unique waveform that allows the individual fish to identify between species, genders, individuals and even between mates with better fitness levels.[33] The differences include the direction of the initial phase of the wave (positive or negative, which correlates to the direction of the current through the electrocytes in the electric organ), the amplitude of the wave, the frequency of the wave, and the number of phases of the wave.

One significant force driving this evolution is predation.[34] The most common predators of Gymnotiformes include the closely related Siluriformes (catfish), as well as predation within families (E. electricus is one of the largest predators of Gymnotus). These predators sense electric fields, but only at low frequencies, thus certain species of Gymnotiformes, such as those in Gymnotus, have shifted the frequency of their signals so they can be effectively invisible.[34][35][36]

Sexual selection is another driving force with an unusual influence, in that females exhibit preference for males with low-frequency signals (which are more easily detected by predators),[34] but most males exhibit this frequency only intermittently. Females prefer males with low-frequency signals because they indicate a higher fitness of the male.[37] Since these low-frequency signals are more conspicuous to predators, the emitting of such signals by males shows that they are capable of evading predation.[37] Therefore, the production of low-frequency signals is under competing evolutionary forces: it is selected against due to the eavesdropping of electric predators, but is favored by sexual selection due to its attractiveness to females. Females also prefer males with longer pulses,[33] also energetically expensive, and large tail lengths. These signs indicate some ability to exploit resources,[34] thus indicating better lifetime reproductive success.

Genetic drift is also a factor contributing to the diversity of electric signals observed in Gymnotiformes.[38] Reduced gene flow due to geographical barriers has led to vast differences signal morphology in different streams and drainages.[38]

See also

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References

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  1. ^ Froese, Rainer; Pauly, Daniel (eds.). "Order Gymnotiformes". FishBase. Apr 2007 version.
  2. ^ van der Sleen, P.; Albert, J. S., eds. (2017). Field Guide to the Fishes of the Amazon, Orinoco, and Guianas. Princeton University Press. pp. 322–345. ISBN 978-0691170749.
  3. ^ a b Ferraris, Carl J. (1998). Paxton, J.R.; Eschmeyer, W.N. (eds.). Encyclopedia of Fishes. San Diego: Academic Press. pp. 111–112. ISBN 0-12-547665-5.
  4. ^ Youngerman, Eric D.; Flammang, Brooke E.; Lauder, George V. (October 2014). "Locomotion of free-swimming ghost knifefish: anal fin kinematics during four behaviors". Zoology. 117 (5): 337–348. Bibcode:2014Zool..117..337Y. doi:10.1016/j.zool.2014.04.004. PMID 25043841.
  5. ^ a b Shirgaonkar, Anup A.; Curet, Oscar M.; Patankar, Neelesh A.; MacIver, Malcolm A. (1 November 2008). "The hydrodynamics of ribbon-fin propulsion during impulsive motion". Journal of Experimental Biology. 211 (21): 3490–3503. doi:10.1242/jeb.019224. PMID 18931321. S2CID 10911068.
  6. ^ Neveln, I. D.; Bale, R.; Bhalla, A. P. S.; Curet, O. M.; Patankar, N. A.; MacIver, M. A. (15 January 2014). "Undulating fins produce off-axis thrust and flow structures". Journal of Experimental Biology. 217 (2): 201–213. doi:10.1242/jeb.091520. PMID 24072799. S2CID 2656865.
  7. ^ a b c Neveln, I. D.; Bai, Y.; Snyder, J. B.; Solberg, J. R.; Curet, O. M.; Lynch, K. M.; MacIver, M. A. (1 July 2013). "Biomimetic and bio-inspired robotics in electric fish research". Journal of Experimental Biology. 216 (13): 2501–2514. doi:10.1242/jeb.082743. PMID 23761475. S2CID 14992273.
  8. ^ a b Xiong, Grace; Lauder, George V. (August 2014). "Center of mass motion in swimming fish: effects of speed and locomotor mode during undulatory propulsion". Zoology. 117 (4): 269–281. Bibcode:2014Zool..117..269X. doi:10.1016/j.zool.2014.03.002. PMID 24925455.
  9. ^ Salazar, R.; Fuentes, V.; Abdelkefi, A. (January 2018). "Classification of biological and bioinspired aquatic systems: A review". Ocean Engineering. 148: 75–114. Bibcode:2018OcEng.148...75S. doi:10.1016/j.oceaneng.2017.11.012.
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  12. ^ Crampton, W.G.R. and J.S. Albert. 2006. Evolution of electric signal diversity in gymnotiform fishes. Pp. 641–725 in Communication in Fishes. F. Ladich, S.P. Collin, P. Moller & B.G Kapoor (eds.). Science Publishers Inc., Enfield, NH.
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  15. ^ a b Albert, J. S., and W. G. R. Crampton. 2005. Electroreception and electrogenesis. Pp. 431–472 in The Physiology of Fishes, 3rd Edition. D. H. Evans and J. B. Claiborne (eds.). CRC Press.
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  19. ^ "Fink and Fink, 1996">Fink, Sara V.; Fink, William L. (August 1981). "Interrelationships of the ostariophysan fishes (Teleostei)". Zoological Journal of the Linnean Society. 72 (4): 297–353. doi:10.1111/j.1096-3642.1981.tb01575.x.
  20. ^ "Arcila et al., 2017">Arcila, Dahiana; Ortí, Guillermo; Vari, Richard; Armbruster, Jonathan W.; Stiassny, Melanie L. J.; Ko, Kyung D.; Sabaj, Mark H.; Lundberg, John; Revell, Liam J.; Betancur-R, Ricardo (13 January 2017). "Genome-wide interrogation advances resolution of recalcitrant groups in the tree of life". Nature Ecology & Evolution. 1 (2): 20. Bibcode:2017NatEE...1...20A. doi:10.1038/s41559-016-0020. PMID 28812610. S2CID 16535732.
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  24. ^ Lavoué, Sébastien; Miya, Masaki; Arnegard, Matthew E.; Sullivan, John P.; Hopkins, Carl D.; Nishida, Mutsumi (14 May 2012). Murphy, William J. (ed.). "Comparable Ages for the Independent Origins of Electrogenesis in African and South American Weakly Electric Fishes". PLOS ONE. 7 (5): e36287. Bibcode:2012PLoSO...736287L. doi:10.1371/journal.pone.0036287. PMC 3351409. PMID 22606250.
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  26. ^ Albert, James S.; Fink, William L. (12 March 2007). "Phylogenetic relationships of fossil neotropical electric fishes (Osteichthyes: Gymnotiformes) from the upper Miocene of Bolivia". Journal of Vertebrate Paleontology. 27 (1): 17–25. doi:10.1671/0272-4634(2007)27[17:PROFNE]2.0.CO;2. S2CID 35007130.
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  30. ^ Hopkins, Carl D (1 December 1995). "Convergent designs for electrogenesis and electroreception". Current Opinion in Neurobiology. 5 (6): 769–777. doi:10.1016/0959-4388(95)80105-7. PMID 8805421. S2CID 39794542.
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  32. ^ Arnegard, Matthew E.; Bogdanowicz, Steven M.; Hopkins, Carl D. (February 2005). "Multiple cases of striking genetic similarity between alternate electric fish signal morphs in sympatry". Evolution. 59 (2): 324–343. doi:10.1111/j.0014-3820.2005.tb00993.x. PMID 15807419. S2CID 14178144.
  33. ^ a b Arnegard, Matthew E.; McIntyre, Peter B.; Harmon, Luke J.; Zelditch, Miriam L.; Crampton, William G. R.; Davis, Justin K.; Sullivan, John P.; Lavoué, Sébastien; Hopkins, Carl D. (1 September 2010). "Sexual Signal Evolution Outpaces Ecological Divergence during Electric Fish Species Radiation". The American Naturalist. 176 (3): 335–356. doi:10.1086/655221. PMID 20653442. S2CID 16787431.
  34. ^ a b c d Hopkins, C. D. (15 May 1999). "Design features for electric communication". Journal of Experimental Biology. 202 (10): 1217–1228. doi:10.1242/jeb.202.10.1217. PMID 10210663.
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  36. ^ Stoddard, Philip K. (1 September 2002). "The evolutionary origins of electric signal complexity". Journal of Physiology-Paris. 96 (5): 485–491. doi:10.1016/S0928-4257(03)00004-4. PMID 14692496. S2CID 6240530.
  37. ^ a b Stoddard, Philip K.; Tran, Alex; Krahe, Rüdiger (10 July 2019). "Predation and Crypsis in the Evolution of Electric Signaling in Weakly Electric Fishes". Frontiers in Ecology and Evolution. 7: 264. doi:10.3389/fevo.2019.00264. S2CID 195856052.
  38. ^ a b Picq, Sophie; Alda, Fernando; Bermingham, Eldredge; Krahe, Rüdiger (September 2016). "Drift-driven evolution of electric signals in a Neotropical knifefish". Evolution. 70 (9): 2134–2144. doi:10.1111/evo.13010. PMID 27436179. S2CID 1064883.
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