Fish locomotion

The prevailing type of fish locomotion is swimming in water. In addition, some fish can "walk", i.e., move over land, burrow in mud, and glide through the air.

Swimming

Fish swim by exerting force against the surrounding water. There are exceptions, but this is normally achieved by the fish contracting muscles on either side of its body in order to generate waves of flexion that travel the length of the body from nose to tail, generally getting larger as they go along. The vector forces exerted on the water by such motion cancel out laterally, but generate a net force backwards which in turn pushes the fish forward through the water.

Most fishes generate thrust using lateral movements of their body and caudal fin. But there are also a huge number of species that move mainly using their median and paired fins. The latter group profits from the gained maneuverability that is needed when living in coral reefs for example. But they can't swim as fast as fish using their bodies and caudal fins.

Body/caudal fin propulsion

There are five groups that differ in the fraction of their body that is displaced laterally:[1]

Anguilliform locomotion

In some long, slender fish – eels, for example – there is little increase in the amplitude of the flexion wave as it passes along the body.

Sub-carangiform locomotion

Here, there is a more marked increase in wave amplitude along the body with the vast majority of the work being done by the rear half of the fish. In general, the fish body is stiffer, making for higher speed but reduced maneuverability. Trout use sub-carangiform locomotion.

Carangiform locomotion

Fish in this group are stiffer and faster-moving than the previous groups. The vast majority of movement is concentrated in the very rear of the body and tail. Carangiform swimmers generally have rapidly oscillating tails.

Thunniform locomotion

The next-to-last group is reserved for the high-speed long-distance swimmers, like tuna (new research shows that the thunniform locomotion is a unique trait of the tunas[2]). Here, virtually all the sideways movement is in the tail and the region connecting the main body to the tail (the peduncle). The tail itself tends to be large and crescent shaped.

Ostraciiform locomotion

These fishes have no appreciable body wave when they employ caudal locomotion. Only the tail fin itself oscillates (often very rapidly) to create thrust. This group includes Ostraciidae.

Median/paired fin propulsion

Not all fish fit comfortably in the above groups. Ocean sunfish, for example, have a completely different system, and many small fish use their pectoral fins for swimming as well as for steering and dynamic lift. Fish with electric organs, such as those in Gymnotiformes, swim by undulating their fins while keeping the body still, presumably so as not to disturb the electric field that they generate.

Dynamic lift

Bone and muscle tissues of fish are denser than water. To maintain depth some fish increase buoyancy by means of a gas bladder or by storing oils or lipids. Fish without these features use dynamic lift instead. It is done using their pectoral fins in a manner similar to the use of wings by airplanes and birds. As these fish swim, their pectoral fins are positioned to create lift which allows the fish to maintain a certain depth.

Sharks are a notable example of fish that depend on dynamic lift; notice their well-developed pectoral fins.

The two major drawbacks of this method are that these fish must stay moving to stay afloat and that they are incapable of swimming backwards or hovering.

Hydrodynamic principles

Similarly to the aerodynamics of flight, powered swimming requires animals to overcome drag by producing thrust. Unlike flying, however, swimming animals do not necessarily need to actively exert high vertical forces because the effect of buoyancy can counter the downward pull of gravity, allowing these animals to float without much effort. While there is great diversity in fish locomotion, swimming behavior can be classified into two distinct "modes" based on the body structures involved in thrust production, Median-Paired Fin (MPF) and Body-Caudal Fin (BCF). Within each of these classifications, there are a numerous specifications along a spectrum of behaviours from purely undulatory to entirely oscillatory based. In undulatory swimming modes thrust is produced by wave-like movements of the propulsive structure (usually a fin or the whole body). Oscillatory modes, on the other hand, are characterized by thrust production from swiveling of the propulsive structure on an attachment point without any wave-like motion.[3]

A bright yellow boxfish swims with its pectoral fins only.
Boxfish are the classic biological example of MPF swimming because they are not well streamlined and use primarily their pectoral fins for thrust production.

Median-paired fin

Many fish swim using combined behavior of their two pectoral fins or both their anal and dorsal fins. Different types of Median paired fin propulsion can be achieved by preferentially using one fin pair over the other, and include:[3]

Undulatory
Oscillatory
Sardines swim in an aquarium tank.
Sardines use body-caudal fin propulsion to swim and hold their pectoral, dorsal, and anal fins flat against the body, creating a more streamlined body and reducing drag.

Body-caudal fin

Most fish swim by generating undulatory waves that propagate down the body through the caudal fin. This form of undulatory locomotion is termed Body-Caudal Fin (BCF) swimming on the basis of the body structures used.[3][5]

Undulatory
Oscillatory

Adaptation

Similar to adaptation in avian flight, swimming behaviors in fish can be thought of as a balance of stability and maneuverability.[7] Because BCF swimming relies on more caudal body structures that can direct powerful thrust only rearwards, this form of locomotion is particularly effective for accelerating quickly and cruising continuously.[3][5] BCF swimming is, therefore, inherently stable and is often seen in fish with large migration patterns that must maximize efficiency over long periods. Propulsive forces in MPF swimming, on the other hand, are generated by multiple fins located on either side of the body that can be coordinated to execute elaborate turns. As a result, MPF swimming is well adapted for high maneuverability and is often seen in smaller fish that require elaborate escape patterns.[7]

The habitats occupied by fishes are often related to their swimming capabilties. Coral reefs typically have faster-swimming fish species living in wave-swept habitats subject to fast water flow speeds, while the slower fishes live in sheltered habitats with low levels of water movement.[8]

It is important to point out that fish do not rely exclusively on one locomotor mode, but are rather locomotor "generalists,"[3] choosing among and combining behaviors from many available behavioral techniques. In fact, at slower speeds, predominantly BCF swimmers will often incorporate movement of their pectoral, anal, and dorsal fins as an additional stabilizing mechanism at slower speeds,[9] but hold them close to their body at high speeds to improve streamlining and reducing drag.[3] Zebrafish have even been observed to alter their locomotor behavior in response to changing hydrodynamic influences throughout growth and maturation.[10]

In addition to adapting locomotor behavior, controlling buoyancy effects is critical for aquatic survival since aquatic ecosystems vary greatly by depth. Fish generally control their depth by regulating the amount of gas in specialized organs that are much like balloons. By changing the amount of gas in these swim bladders, fish actively control their density. If they increase the amount of air in their swim bladder, their overall density will become less than the surrounding water, and increased upward buoyancy pressures will cause the fish to rise until they reach a depth at which they are again at equilibrium with the surrounding water. In this way, fish behave essentially as a hot air balloon does in air.

Flying

The transition of predominantly swimming locomotion directly to flight has evolved in a single family of marine fish called Exocoetidae. Flying fish are not true fliers in the sense that they do not execute powered flight. Instead, these species glide directly over the surface of the ocean water without ever flapping their "wings." Flying fish have evolved abnormally large pectoral fins that act as airfoils and provide lift when the fish launches itself out of the water. Additional forward thrust and steering forces are created by dipping the hypocaudal (i.e. bottom) lobe of their caudal fin into the water and vibrating it very quickly, in contrast to diving birds in which these forces are produced by the same locomotor module used for propulsion. Of the 64 extant species of flying fish, only two distinct body plans exist, each of which optimizes two different behaviors.[11][12]

remains of a flying fish are displayed in glass box.
Flying fish are able to achieve sufficient lift to glide above the surface of the water thanks to their enlarged pectoral fins.

Tradeoffs

Tail Structure: While most fish have caudal fins with evenly sized lobes (i.e. homocaudal), flying fish have an enlarged ventral lobe (i.e. hypocaudal) which facilitates dipping only a portion of the tail back onto the water for additional thrust production and steering.[12]

Larger mass: Because flying fish are primarily aquatic animals, their body density must be close to that of water for buoyancy stability. This primary requirement for swimming, however, means that flying fish are heavier than other habitual fliers, resulting in higher wing loading and lift to drag ratios for flying fish compared to a comparably sized bird.[11] Differences in wing area, wing span, wing loading, and aspect ratio have been used to classify flying fish into two distinct classifications based on these different aerodynamic designs.[11]

Biplane body plan

In the biplane or cypselurus body plan, both the pectoral and pelvic fins are enlarged to provide lift during flight.[11] These fish also tend to have "flatter" bodies which increase the total lift producing area thus allowing them to "hang" in the air better than more streamlined shapes.[12] As a result of this high lift production, these fish are excellent gliders and are well adapted for maximizing flight distance and duration.

Comparatively, Cypselurus flying fish have lower wing loading and smaller aspect ratios (i.e. broader wings) than their Exocoetus monoplane counterparts, which contributes to their ability to fly for longer distances than fish with this alternative body plan. Flying fish with the biplane design take advantage of their high lift production abilities when launching from the water by utilizing a "taxiing glide" in which the hypocaudal lobe remains in the water to generate thrust even after the trunk clears the water's surface and the wings are opened with a small angle of attack for lift generation.[11]

illustration of a typical flying fish body plan
In the monoplane body plan, only the pectoral fins are abnormally large. In this illustration, note that the pelvic fins are not abnormally large.

Monoplane body plan

In the Exocoetus or monoplane body plan, only the pectoral fins are enlarged to provide lift. Fish with this body plan tend to have a more streamlined body, higher aspect ratios (long, narrow wings), and higher wing loading than fish with the biplane body plan, making these fish well adapted for higher flying speeds. Flying fish with a monoplane body plan demonstrate different launching behaviors from their biplane counterparts. Instead of extending their duration of thrust production, monoplane fish launch from the water at high speeds at a large angle of attack (sometimes up to 45 degrees).[11] In this way, monoplane fish are taking advantage of their adaptation for high flight speed, while fish with biplane designs exploit their lift production abilities during takeoff.

Walking

Main article: Walking fish
Alticus arnoldorum hopping
Alticus arnoldorum climbing up a vertical piece of Plexiglas

A "walking fish" is a fish that is able to travel over land for extended periods of time. Some other cases of nonstandard fish locomotion include fish "walking" along the sea floor, such as the handfish or frogfish.

Most commonly, walking fish are amphibious fish. Able to spend longer times out of water, these fish may use a number of means of locomotion, including springing, snake-like lateral undulation, and tripod-like walking. The mudskippers are probably the best land-adapted of contemporary fish and are able to spend days moving about out of water and can even climb mangroves, although to only modest heights.[13] The Climbing gourami is often specifically referred to as a "walking fish", although it does not actually "walk", but rather moves in a jerky way by supporting itself on the extended edges of its gill plates and pushing itself by its fins and tail. Some reports indicate that it can also climb trees.[14]

There are a number of fish that are less adept at actual walking, such as the walking catfish. Despite being known for "walking on land", this fish usually wriggles and may use its pectoral fins to aid in its movement. Walking Catfish have a respiratory system that allows them to live out of water for several days. Some are invasive species. A notorious case in the United States is the Northern snakehead.[15] Polypterids have rudimentary lungs and can also move about on land, though rather clumsily. The Mangrove rivulus can survive for months out of water and can move to places like hollow logs.[16][17][18][19]

Ogcocephalus parvus

There are some species of fish that can "walk" along the sea floor but not on land; one such animal is the flying gurnard (it does not actually fly, and should not be confused with flying fish). The batfishes of the Ogcocephalidae family (not to be confused with Batfish of Ephippidae) are also capable of walking along the sea floor. Bathypterois grallator, also known as a "tripodfish", stands on its three fins on the bottom of the ocean and hunts for food.[20] The African lungfish (P. annectens) can use its fins to "walk" along the bottom of its tank in a manner similar to the way amphibians and land vertebrates use their limbs on land. [21][22][23]

Burrowing

Many fishes, particularly eel-shaped fishes such as true eels, moray eels, and spiny eels, are capable of burrowing through sand or mud.[24] Ophichthids are capable of digging backwards using a sharpened tail.

See also

References

  1. ↑ Breder CM (1926) "The locomotion of fishes", Zoologica, 4: 159–297.
  2. ↑ Hawkins JD, CA Sepulveda, JB Graham and KA Dickson (2003) "Swimming performance studies on the eastern Pacific bonito Sarda chiliensis, a close relative of the tunas (family Scombridae) II. Kinematics" The Journal of Experimental Biology, 206: 2749-2758.
  3. 1 2 3 4 5 6 Sfakiotakis M, Lane DM and Davies JBC (1999) "Review of Fish Swimming Modes for Aquatic Locomotion" IEEE Journal of Oceanic Engineering, 24 (2).
  4. ↑ Fulton CJ, Johansen JL, Steffensen JF (2013) Energetic extremes in aquatic locomotion by coral reef fishes. PLoS One 8, e54033
  5. 1 2 Blake, R.W. (2004) Review Paper: Fish functional design and swimming performance. Journal of Fish Biology 65, pp 1193-1222.
  6. ↑ Long Jr, J. H., Shepherd, W., & Root, R. G. (1997). Manueuverability and reversible propulsion: How eel-like fish swim forward and backward using travelling body waves". In: Proc. Special Session on Bio-Engineering Research Related to Autonomous Underwater Vehicles, 10th Int. Symp. Unmanned Untethered Submersible Technology (pp. 118-134).
  7. 1 2 Weihs, Daniel. (2002) Stability versus Maneuverability in Aquatic Locomotion. Integrated and Computational Biology. 42, 127-134.
  8. ↑ Fulton CJ, Bellwood DR, Wainwright PC (2005) Wave energy and swimming performance shape coral reef fish assemblages. Proceedings of the Royal Society B 272, 827-832
  9. ↑ Heatwole SJ, Fulton CJ (2013) Behavioural flexibility in coral reef fishes responding to a rapidly changing environment. Marine Biology 160, 677-689
  10. ↑ , Matthew J. and George V. Lauder. (2006) Otogeny of Form and Function: Locomotor Morphology and Drag in Zebrafish (Danio rerio). "Journal of Morphology." 267,1099-1109.
  11. 1 2 3 4 5 6 Fish, F.E. (1990) Wing design and scaling of flying fish with regard to flight performance. "J. Zool. Lond." 221, 391-403.
  12. 1 2 3 Fish, Frank. (1991) On a Fin and a Prayer. "Scholars." 3(1), 4-7.
  13. ↑ http://www.cairnsmuseum.org.au/tourism.htm
  14. ↑ Climbing Fish
  15. ↑ "Maryland Suffers Setback in War on Invasive Walking Fish", National Geographic News July 12, 2002
  16. ↑ Shells, trees and bottoms: Strange places fish live
  17. ↑ "Tropical fish can live for months out of water". Reuters. 15 November 2007.
  18. ↑ Fish Lives in Logs, Breathing Air, for Months at a Time
  19. ↑ Fish Lives in Logs, Breathing Air, for Months at a Time
  20. ↑ Jones, AT; KJ Sulak (1990). "First Central Pacific Plate and Hawaiian Record of the Deep-sea Tripod Fish Bathypterois grallator (Pisces: Chlorophthalmidae)" (PDF). Pacific Science 44 (3): 254–7.
  21. ↑ Fish uses fins to walk and bound
  22. ↑ Behavioral evidence for the evolution of walking and bounding before terrestriality in sarcopterygian fishes
  23. ↑ A Small Step for Lungfish, a Big Step for the Evolution of Walking
  24. ↑ Monks, Neale (2006). Brackish-Water Fishes. TFH. pp. 223–226. ISBN 0-7938-0564-3.

Further reading

External links

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