Migration is a word used in multiple senses. It is important to distinguish "true" migration, i.e. a life-history-structured or at least patterned activity such as seen in ''anadromous'' species like salmons, from mere movement or wandering as may happen, say, with ''euryhaline'' species that easily move between fresh and salt water but not necessarily or with regularity. "Vertical migration", for example, the phenomenon of plankton and fishes regularly changing their depth throughout the 24h day, is a special usage unlike migrations of (e.g.) salmons that range over distances in migrations that may cover river, lake, and sea, or the great migrations of game through Africa's Serengeti.
''Anadromous'' and ''catadromous'' are words that have been commonly used for centuries. They are slightly more narrowly used in the following classification of [truly] migrating fish by Myers 1949:
:"''Diadromous''. Truly migratory fishes which migrate between the sea and fresh water. There has been no English term by which one can refer collectively and briefly to anadromous, catadromous and other fishes which truly migrate between fresh and salt water, and this new term is now proposed ... . Like the two well known ones, this adjective is formed from classical Greek ([dia], through; and [dromous], running). ...
:''Anadromous''. Diadromous fishes which spend most of their lives in the sea and migrate to fresh water to breed (From [ana], up ...). ... [This narrowed the previous usage which could apply to fish never crossing the freswater/sea boundary but simply moving upstream to spawn, for example in some fishes of the Rift Lakes]
:''Catadromous''. Diadromous fishes which spend most of their lives in fresh water and migrate to the sea to breed. (From [cata], down ...). ... [This narrowed the previous usage which could apply to fish never reaching the sea but moving downstream to spawn]
:''Amphidromous''. Diadromous fishes whose migration from fresh water to the seas, or vice versa, is not for the purpose of breeding, but occurs regularly at some other stage of the life cycle. (From [amphi], around, on both sides ...) ... [The elements "vice versa" and "purpose" are troublesome however]
:''Potamodromous''. Truly migratory fishes whose migrations occur wholly within freshwater. (From [potamos], river ... ) ... [Rarely used. This term and ''oceanodromous'' received the fishes excluded by the narrowing of ''anadromous'' and ''catadromous'']
:''Oceanodromous''. Truly migratory fishes which live and migrate wholly in the sea. (From [oceanos], the ocean ... ) ... [Rarely used. This term and ''potamodromous'' received the fishes excluded by the narrowing of ''anadromous'' and ''catadromous''] ”
The "-ous" endings are for the adjectival form of the terms; nouns are obtained by replacing that ending with "-y", e.g. ''anadromy''.
The terms ''anadromous'' and ''catadromous'' were of long standing (and similar but not identical usage); the other terms were coined by Myers. Myers was hesitant about introducing new terms however, saying:
:"The writer's strong aversion to the infliction of new scientific terms upon the scientific public has, however, caused him to proceed with great circumspection. ... Finally, the writer has ventured to propose new terms only because he feels that certain new terms will be of distinct advantage in some specialized types of ichthyological work, and that the general biologist and fishery worker will seldom or never have to bother his head about them. Catadromous and anadromous will almost certainly always remain the most important and ''probably the only widely used'' terms of their class."(emphasis added)
Myers' term ''diadromous'' has proved useful as an inclusive term. But his prediction was otherwise accurate: ''anadromous'' and ''catadromous'', are indeed the main widely understood terms. Secor and Kerr (2009) found only one paper that used ''oceanodromous'', 18 using ''potamodromous'', and 122 using ''amphidromous'' compared to 985 times for ''anadromous'', 143 times for ''diadromous'', 71 times for ''catadromous''. Obviously the amount of work done on a group is one source of this variation, but another source is the perceived utility and standing of the term itself.
''Amphidromy'' is rarely understood by the wider fish biology audience, or alternatively "There seems to be some reluctance to use the term amphidromy". Myers' definition's ambiguity ("or vice versa") and teleology ("for the purpose of") is one part of that problem. Its meaning/usage has been adjusted (but two such adjustments were found zero times by Secor and Kerr (2009)), and recently it has been stated as differing from ''anadromy'' simply because return to fresh water occurs at a juvenile or immature stage; other differences have been claimed (such as where most growth occurs) but they are necessary consequences of the stage at return and therefore are not independent. Some authors have therefore eschewed ''amphidromy'' in favour of the more widely understood terms: either ''anadromy'', with or without a remark that return to rivers occurs at an earlier stage (e.g. "juvenile-return anadromy" ), or ''diadromy'' which discards information that would be conveyed by ''anadromy'' with or without remark.
It has to be borne in mind that any typological system has heuristic value as a convenience for description, and need not reflect phylogeny: each category (term) may include representatives of many distantly related taxa, each of which may well have close relatives that are in another category (term) or that are not migratory and thus fall completely outside the typology. These terms are therefore of limited safety when used alone to screen data to be considered for an analysis, or to decide which species should be read about to explore a phenomenon or possible comparison.
The limitations of typologies were clearly stated by Myers himself. Each may be useful in one context, for one purpose, but not another. I.e. they may categorise along different axes (see Secor and Kerr (2009)). For example, Myers in the same year devised another interesting set of terms, also directed at fishes, but on the basis of their salt-tolerance.
As a footnote it is interesting to note that George S. Myers had previously been one of the degree supervisors for Porfirio Manacop, whose ground-breaking Master's work (in 1941, later published 1953) on a ''Sicyopterus'' species overturned the prevailing notion that it was catadromous. It is likely that Myers was impressed by this, and used ''Sicydium'' as the "type" genus for ''amphidromous''.
And, as a contrary footnote showing how science fails: regrettably, Manacop's work seems to have been as locally unpopular as it was innovative, because over 20 years later the group he worked on was still being referred to by a colleague in the Philippines who would certainly have known of his work, incorrectly and without evidence, as ''catadromous''.
And although these systems were originated for fishes, they are in principle applicable to any organism.
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 have 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.
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 in September to November. The spawning migration starts north of Iceland in December or January.
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.
These high trophic 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 mile 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.
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.
The most remarkable catadromous fishes are freshwater eels of genus ''Anguilla'', whose larvae drift from swawning grounds in the Sargasso sea, sometimes for months or years, before entering freshwater river and streams as glass eels or elvers (see ''eel life history'').
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 fish migrations are usually shorter, typically from lake to stream or vice versa, for spawning purposes. However, potamodromous migrations of Colorado pikeminnow of the Colorado River system can be extensive. Migrations to natal spawning grounds easily be 100 km, with maximum distances of 300 km reported from radiotagging studies.
Category:Ichthyology Category:Aquatic ecology Category:Fisheries
cs:Migrace ryb de:Wanderfisch et:Anadroomne ränne fr:Migration des poissons ko:회유 id:Migrasi ikan it:Migrazione ittica kk:Анадромды жылыстау nl:Anadroom ja:回遊 no:Anadromi nn:Anadromi pt:Migração de peixes ru:Миграция рыб sv:Fiskvandring th:ปลาน้ำกร่อย tr:Göçmen balıklar vi:Sự di cư của cáThis text is licensed under the Creative Commons CC-BY-SA License. This text was originally published on Wikipedia and was developed by the Wikipedia community.
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