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Fish migration

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(Redirected from Anadromy)
"Anadromy" redirects here. Not to be confused with Anadrome.
Many species of salmon are anadromous and can migrate long distances up rivers to spawn
Allowing fish and other migratory animals to travel the rivers can help maintain healthy fish populations

Fish migration is mass relocation by fish from one area or body of water to another. Many types of fish migrate on a regular basis, on time scales ranging from daily to annually or longer, and over distances ranging from a few metres to thousands of kilometres. Such migrations are usually done for better feeding or to reproduce, but in other cases the reasons are unclear.

Fish migrations involve movements of schools of fish on a scale and duration larger than those arising during normal daily activities.[1] Some particular types of migration are anadromous, in which adult fish live in the sea and migrate into fresh water to spawn; and catadromous, in which adult fish live in fresh water and migrate into salt water to spawn.[2]

Marine forage fish often make large migrations between their spawning, feeding and nursery grounds. Their movements are associated with ocean currents and with the availability of food in different areas at different times of the year. The migratory movements may partly be linked to the fact that the fish cannot identify their own offspring and moving in this way prevents cannibalism. Some species have been described by the United Nations Convention on the Law of the Sea as highly migratory species. These are large pelagic fish that move in and out of the exclusive economic zones of different nations, and these are covered differently in the treaty from other fish.

Salmon and striped bass are well-known anadromous fish, and freshwater eels are catadromous fish that make large migrations. The bull shark is a euryhaline species that moves at will from fresh to salt water, and many marine fish make a diel vertical migration, rising to the surface to feed at night and sinking to lower layers of the ocean by day. Some fish such as tuna move to the north and south at different times of year following temperature gradients. The patterns of migration are of great interest to the fishing industry. Movements of fish in fresh water also occur; often the fish swim upriver to spawn, and these traditional movements are increasingly being disrupted by the building of dams.[3]

Classification

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Ocean migration of Atlantic salmon from Connecticut River[4]

As with various other aspects of fish life, zoologists have developed empirical classifications for fish migrations.[5] The first two following terms have been in long-standing wide usage, while others are of more recent coinage.

  • Anadromous – fish that migrate from the sea up (Greek: ἀνά aná, "up" and δρόμος drómos, "course") into fresh water to spawn, such as salmon, striped bass,[6] and the sea lamprey[7]
  • Catadromous – fish that migrate from fresh water down (Greek: κατά kata, "down" and δρόμος dromos, "course") into the sea to spawn, such as eels[6][8]

George S. Myers coined the following terms in a 1949 journal article:

  • Diadromous – all fish that migrate between the sea and fresh water. Like the two aforementioned, well-known terms, diadromous was formed from Classical Greek ([dia], "through"; and [dromous], "running").
  • Amphidromous – fish that migrate from fresh water to the sea, or vice versa, but not for the purpose of breeding. Instead they enter saltwater or freshwater as larvae, where they will grow into juveniles before returning to the habitat they originally came from and stay there for the rest of their life, growing into sexually mature adults.[9]
  • Potamodromous – fish whose migrations occur wholly within fresh water
  • Oceanodromous – fish that live and migrate wholly in the sea[5][10]

Although these classifications originated for fish, they can apply, in principle, to any aquatic organism.

List of diadromous orders and families, and the number of known species:[9][11]

Clade Order Family Diadromous Anadromous Catadromous Amphidromous
Cyclostomi Lampreys Geotriidae 1 1
Mordaciidae 2 2
Petromyzontidae 8 8
Chondrostei Acipenseriformes Sturgeons 18 18
Elopomorpha Elopiformes Elopidae 1 1
Tarpons 1 1
Eels Anguillidae 16 16
Moray eels 1 1
Ophichthidae 1 1
Otocephala Clupeiformes Clupeidae 31 26 2 3
Anchovies 11 5 1 5
Pristigasteridae 7 4 3
Cypriniformes Cyprinidae 6 6
Characiformes Citharinidae 2 2
Catfish Ariidae 13 3 10
Bagridae 1 1
Claroteidae 1 1
Shark catfish 1 1
Eeltail catfish 1 1
Schilbeidae 1 1
Protacanthopterygii Galaxiiformes Galaxiidae 11 1 10
Salmoniformes Salmonidae 35 35
Stomiati Osmeriformes Smelts 10 10
Plecoglossidae 1 1
Retropinnidae 5 1 4
Salangidae 6 6
Paracanthopterygii Gadiformes Gadidae 1 1
Lotidae 1 1
Percomorpha Ovalentaria Ambassidae 4 1 3
Atheriniformes Old World silversides 1 1
Neotropical silversides 2 2
Gobiesociformes Gobiesocidae 1 1
Gobiiformes Eleotridae 37 5 32
Gobiidae 103 2 101
Rhyacichthyidae 2 2
Mugiliformes Mugilidae 34 1 27 6
Flatfish Pleuronectidae 2 2
Syngnathiformes Syngnathidae 5 5
Tetraodontiformes Tetraodontidae 2 2
Carangiformes Carangidae 2 2
Moroniformes Moronidae 2 2
Acanthuriformes Sciaenidae 3 3
Scorpaeniformes Cottidae 8 2 6
Sticklebacks 2 2
Scorpaenidae
(subfamily Tetraroginae) 		1 1
Trachiniformes Cheimarrichthyidae 1 1
Perciformes Lutjanidae 2 2
Centropomidae 9 2 7
Mojarras 7 7
Haemulidae 1 1
Flagtails 10 5 5
Lateolabracidae 1 1
Latidae 1 1
Temperate perchs 1 1
Percidae 1 1
Pseudaphritidae 1 1
Terapontidae 1 1
Archerfish 3 3
Total 444 147 73 224

Forage fish

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Migration of Icelandic capelin
See also: Sardine run

Forage fish often make great migrations between their spawning, feeding and nursery grounds. Schools of a particular stock usually travel in a triangle between these grounds. For example, one stock of herrings has their spawning ground in southern Norway, their feeding ground in Iceland, and their nursery ground in northern Norway. Wide triangular journeys such as these may be important because forage fish, when feeding, cannot distinguish their own offspring.[3]

Capelin are a forage fish of the smelt family found in the Atlantic and Arctic oceans. In summer, they graze on dense swarms of plankton at the edge of the ice shelf. Larger capelin also eat krill and other crustaceans. The capelin move inshore in large schools to spawn and migrate in spring and summer to feed in plankton rich areas between Iceland, Greenland and Jan Mayen. The migration is affected by ocean currents. Around Iceland, maturing capelin make large northward feeding migrations in spring and summer. The return migration takes place from September to November. The spawning migration starts north of Iceland in December or January.[12]

The diagram on the right shows the main spawning grounds and larval drift routes. Capelin on the way to feeding grounds is coloured green, capelin on the way back is blue, and the breeding grounds are red.

In a paper published in 2009, researchers from Iceland recount their application of an interacting particle model to the capelin stock around Iceland, successfully predicting the spawning migration route for 2008.[13]

Highly migratory species

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The high seas, highlighted in blue, are the seas which are outside the 200 nmi (370 km) exclusive economic zones
See also: Straddling stock and Bonn Convention

The term highly migratory species (HMS) has its origins in Article 64 of the United Nations Convention on the Law of the Sea (UNCLOS). The Convention does not provide an operational definition of the term, but in an annex (UNCLOS Annex 1) lists the species considered highly migratory by parties to the convention.[14] The list includes: tuna and tuna-like species (albacore, bluefin, bigeye tuna, skipjack, yellowfin, blackfin, little tunny, southern bluefin and bullet), wahoo, pomfret, marlin, sailfish, swordfish, saury and oceangoing sharks, dolphins and other cetaceans.

These high trophic level oceanodromous species undertake migrations of significant but variable distances across oceans for feeding, often on forage fish, or reproduction, and also have wide geographic distributions. Thus, these species are found both inside the 200-nautical-mile (370-kilometre) exclusive economic zones and in the high seas outside these zones. They are pelagic species, which means they mostly live in the open ocean and do not live near the sea floor, although they may spend part of their life cycle in nearshore waters.[15]

Highly migratory species can be compared with straddling stock and transboundary stock. Straddling stock range both within an EEZ as well as in the high seas. Transboundary stock range in the EEZs of at least two countries. A stock can be both transboundary and straddling.[16]

It can be challenging to determine the population structure of highly migratory species using physical tagging. Traditional genetic markers such as short-range PCR products, microsatellites and SNP-arrays have struggled to identify population structure and distinguish fish stocks from separate ocean basins. However, population genomic research using RAD sequencing in yellowfin tuna,[17][18] albacore,[19][20] and wahoo[21] has been able to distinguish populations from different ocean basins and reveal fine-scale population structure. Similar population genomics methods have also provided improved insight towards population structure in striped marlin.[22]

Other examples

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See also: Salmon run, Vertical migration, and Lessepsian migration

Some of the best-known anadromous fishes are the Pacific salmon species, such as Chinook (king), coho (silver), chum (dog), pink (humpback) and sockeye (red) salmon. These salmon hatch in small freshwater streams. From there they migrate to the sea to mature, living there for two to six years. When mature, the salmon return to the same streams where they were hatched to spawn. Salmon are capable of going hundreds of kilometers upriver, and humans must install fish ladders in dams to enable the salmon to get past. Other examples of anadromous fishes are sea trout, three-spined stickleback, sea lamprey and [7] shad.

Several Pacific salmon (Chinook, coho and Steelhead) have been introduced into the US Great Lakes, and have become potamodromous, migrating between their natal waters to feeding grounds entirely within fresh water.

Life cycle of anadromous fish. From a U.S. Government pamphlet. (Click image to enlarge.)

Remarkable catadromous migrations are made by freshwater eels. Examples are the American eel and the European eel which migrate huge distances from freshwater rivers to spawn in the Sargasso Sea, and whose subsequent larvae can drift in currents for months and even years before returning to their natal rivers and streams as glass eels or elvers.

An example of a euryhaline species is the bull shark, which lives in Lake Nicaragua of Central America and the Zambezi River of Africa. Both these habitats are fresh water, yet bull sharks will also migrate to and from the ocean. Specifically, Lake Nicaragua bull sharks migrate to the Atlantic Ocean and Zambezi bull sharks migrate to the Indian Ocean.

Diel vertical migration is a common behavior; many marine species move to the surface at night to feed, then return to the depths during daytime.

A number of large marine fishes, such as the tuna, migrate north and south annually, following temperature variations in the ocean. These are of great importance to fisheries.

Freshwater (potamodromous) fish migrations are usually shorter, typically from lake to stream or vice versa, for spawning purposes. However, potamodromous migrations of the endangered Colorado pikeminnow of the Colorado River system can be extensive. Migrations to natal spawning grounds can easily be 100 km, with maximum distances of 300 km reported from radiotagging studies.[23] Colorado pikeminnow migrations also display a high degree of homing and the fish may make upstream or downstream migrations to reach very specific spawning locations in whitewater canyons.[8]

Sometimes fish can be dispersed by birds that eat fish eggs. They carry eggs in the digestive tracts and then deposit them in their faeces in a new place. The survival rate for fish eggs that have passed through a bird's digestive tract is low.[24]

Historic exploitation

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Since prehistoric times humans have exploited certain anadromous fishes during their migrations into freshwater streams, when they are more vulnerable to capture. Societies dating to the Millingstone Horizon are known which exploited the anadromous fishery of Morro Creek[25] and other Pacific coast estuaries. In Nevada the Paiute tribe has harvested migrating Lahontan cutthroat trout along the Truckee River since prehistoric times. This fishing practice continues to current times, and the U.S. Environmental Protection Agency has supported research to assure the water quality in the Truckee can support suitable populations of the Lahontan cutthroat trout.

Myxovirus genes

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Because salmonids live an anadromous lifestyle, they encounter a larger range of viruses from both freshwater and marine ecosystems. Myxovirus resistance (Mx) proteins are part of a GTP-ase family that aid in viral immunity, and previously, rainbow trout (Oncorhynchus mykiss) had been shown to possess three different Mx genes to aid in viral defence in both environments. The number of Mx genes can differ among species of fish, with numbers ranging from 1 to 9 and some outliers like Gadiformes that have totally lost their Mx genes. A study was performed by Wang et al. (2019)[26] to identify more potential Mx genes that resided in rainbow trout. An additional six Mx genes were identified in that study, now named Mx4-9. They also concluded that the trout Mx genes were "differentially expressed constitutively in tissues" and that this expression is increased during development. The Mx gene family is expressed at high levels in the blood and intestine during development, suggesting they are a key to immune defense for the growing fish. The idea that these genes play an important role in development against viruses suggests they are critical in the trout's success in an anadromous lifestyle.

See also

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Notes

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  1. ^ Dingle, Hugh and Drake, V. Alistair (2007) "What Is Migration?". BioScience, 57(2):113–121. doi:10.1641/B570206
  2. ^ Gross, Mart R.; Coleman, Ronald M.; McDowall, Robert M. (1988-03-11). "Aquatic Productivity and the Evolution of Diadromous Fish Migration". Science. 239 (4845): 1291–1293. Bibcode:1988Sci...239.1291G. doi:10.1126/science.239.4845.1291. PMID 17833216. S2CID 241447.
  3. ^ a b Woo, Patrick T. K.; Iwama, George K. (2019-12-21). Climate Change and Non-infectious Fish Disorders. CABI. ISBN 978-1-78639-398-2.
  4. ^ Atlantic Salmon Life Cycle Archived January 15, 2014, at the Wayback Machine Connecticut River Coordinator's Office, U.S. Fish and Wildlife Service.
  5. ^ a b Secor, David H; Kerr L A (2009). "Lexicon of life cycle diversity in diadromous and other fishes". Am. Fish. Soc. Symp. (69): 537–556.
  6. ^ a b Moyle, Peter B.; Cech, Joseph J. (2004). Fishes : an introduction to ichthyology. Upper Saddle River, NJ: Pearson Prentice Hall. ISBN 0-13-100847-1. OCLC 52386194.
  7. ^ a b Silva, S., Araújo, M. J., Bao, M., Mucientes, G., & Cobo, F. (2014). "The haematophagous feeding stage of anadromous populations of sea lamprey Petromyzon marinus: low host selectivity and wide range of habitats". Hydrobiologia, 734(1), 187–199.
  8. ^ a b Tyus, Harold M. (2012). Ecology and conservation of fishes. Boca Raton, FL: CRC Press. ISBN 978-1-4398-9759-1. OCLC 1032266421.
  9. ^ a b Investigating Diadromy in Fishes and Its Loss in an -Omics Era
  10. ^ Myers, George S. (1949). "Usage of Anadromous, Catadromous and allied terms for migratory fishes". Copeia. 1949 (2): 89–97. doi:10.2307/1438482. JSTOR 1438482.
  11. ^ Supplemental Information
  12. ^ Vilhjálmsson, H (October 2002). "Capelin (Mallotus villosus) in the Iceland–East Greenland–Jan Mayen ecosystem". ICES Journal of Marine Science. 59 (5): 870–883. doi:10.1006/jmsc.2002.1233.
  13. ^ Barbaro1 A, Einarsson B, Birnir1 B, Sigurðsson S, Valdimarsson S, Pálsson ÓK, Sveinbjörnsson S and Sigurðsson P (2009) "Modelling and simulations of the migration of pelagic fish" Journal of Marine Science, 66(5):826-838.
  14. ^ United Nations Convention on the Law of the Sea: Text
  15. ^ Pacific Fishery Management Council: Background: Highly Migratory Species
  16. ^ FAO (2007) Report of the FAO workshop on vulnerable ecosystems and destructive fishing in deep sea fisheries, Rome, Fisheries Report No. 829. HTML
  17. ^ Grewe, P.M.; Feutry, P.; Hill, P.L.; Gunasekera, R.M.; Schaefer, K.M.; Itano, D.G.; Fuller, D.W.; Foster, S.D.; Davies, C.R. (2015). "Evidence of discrete yellowfin tuna (Thunnus albacares) populations demands rethink of management for this globally important resource". Scientific Reports. 5: 16916. Bibcode:2015NatSR...516916G. doi:10.1038/srep16916. PMC 4655351. PMID 26593698.
  18. ^ Pecoraro, Carlo; Babbucci, Massimiliano; Franch, Rafaella; Rico, Ciro; Papetti, Chiara; Chassot, Emmanuel; Bodin, Nathalie; Cariani, Alessia; Bargelloni, Luca; Tinti, Fausto (2018). "The population genomics of yellowfin tuna (Thunnus albacares) at global geographic scale challenges current stock delineation". Scientific Reports. 8 (1): 13890. Bibcode:2018NatSR...813890P. doi:10.1038/s41598-018-32331-3. PMC 6141456. PMID 30224658.
  19. ^ Anderson, Giulia; Hampton, John; Smith, Neville; Rico, Ciro (2019). "Indications of strong adaptive population genetic structure in albacore tuna (Thunnus alalunga) in the southwest and central Pacific Ocean". Ecology and Evolution. 9 (18): 10354–10364. doi:10.1002/ece3.5554. PMC 6787800. PMID 31624554.
  20. ^ Vaux, Felix; Bohn, Sandra; Hyde, John R.; O'Malley, Kathleen G. (2021). "Adaptive markers distinguish North and South Pacific Albacore amid low population differentiation". Evolutionary Applications. 14 (5): 1343–1364. doi:10.1111/eva.13202. PMC 8127716. PMID 34025772.
  21. ^ Haro-Bilbao, Isabel; Riginos, Cynthia; Baldwin, John D.; Zischke, Mitchell; Tibbetts, Ian R.; Thia, Joshua A. (2021). "Global connections with some genomic differentiation occur between Indo-Pacific and Atlantic Ocean wahoo, a large circumtropical pelagic fish". Journal of Biogeography. 48 (8): 2053–2067. doi:10.1111/jbi.14135. hdl:11343/298583. ISSN 0305-0270. S2CID 236381627.
  22. ^ Mamoozadeh, Nadya R.; Graves, John E.; McDowell, Jan R. (2020). "Genome-wide SNPs resolve spatiotemporal patterns of connectivity within striped marlin (Kajikia audax), a broadly distributed and highly migratory pelagic species". Evolutionary Applications. 13 (4): 677–698. doi:10.1111/eva.12892. PMC 7086058. PMID 32211060.
  23. ^ Lucas, Martyn C.; Baras, Etienne (2001). Migration of freshwater fishes. Oxford: Blackwell Science. ISBN 978-0-470-99965-3. OCLC 212130719.
  24. ^ "Experiment shows it is possible for fish to migrate via ingestion by birds". phys.org. Retrieved 2020-06-23.
  25. ^ C.M. Hogan, 2008
  26. ^ Wang, T. (2019). "Lineage/species-specific expansion of the Mx gene family in teleosts: Differential expression and modulation of nine Mx genes in rainbow trout Oncorhynchus mykiss". Fish and Shellfish Immunology. 90: 413–430. doi:10.1016/j.fsi.2019.04.303. hdl:2164/14229. PMID 31063803. S2CID 147706565.

References

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Further reading

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Media related to Fish migration at Wikimedia Commons

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