Coryphaena hippurusDorado(Also: Mahi mahi lapa; Mahi mahi oma; Mahihi)

Ge­o­graphic Range

Trop­i­cal and sub­trop­i­cal areas of the At­lantic, Pa­cific, and In­dian Oceans. (Benetti, et al., 1995a)

Habi­tat

In pelagic re­gions, Coryphaena hip­pu­rus is com­monly found near float­ing ob­jects, ap­par­ently be­cause its prey seek refuge under the ob­jects (Palko, et al. 1982).

The dol­phin fish is a top preda­tor in the At­lantic Sar­gas­sum. Com­mon Sar­gas­sum fauna, such as mem­bers of the Bal­is­ti­dae, Carangi­dae, and crabs (De­capoda), have been found in the stom­achs of dol­phin fishes caught there (Beard­s­ley, 1967).

Though it is most fre­quently found in trop­i­cal wa­ters, Coryphaena hip­pu­rus has been de­tected and stud­ied as far north as Ire­land (Quigley, 1996). (Beard­s­ley, 1967; Palko, et al., 1982; Quigley and Flan­nery, 1996)

Phys­i­cal De­scrip­tion

Coryphaena hip­pu­rus has a long, slen­der, ta­pered body spe­cial­ized for swim­ming at high speeds. It has pig­mented pelvic fins and bands of pig­ment lat­er­ally on both the body and me­dian fins. There is a square supra­or­bital re­gion, and the dor­sal fin runs nearly to the bright yel­low cau­dal fin. C. hip­pu­rus is a bright blue-green dor­sally, and yel­low­ish-white with pig­ments ven­trally. Sex­ual di­mor­phism is ev­i­dent, but only no­tice­able after 6 months of age (Benetti, et al. 1995). Males are phys­i­cally larger and heav­ier than fe­males of the same age, and males have a more pro­nounced neu­ro­cra­nium (Ditty, 1994). Dol­phin fish com­monly reach 1 meter in length, but can reach up to 2 me­ters. They usu­ally weight around 14 kg but can weigh more than 30 kg, with a max­i­mum recorded weight of 39.5 kg. (Benetti, et al., 1995a; Ditty, et al., 1994)

  • Sexual Dimorphism
  • male larger
  • sexes shaped differently
  • Range mass
    39.5 (high) kg
    87.00 (high) lb
  • Average mass
    14 kg
    30.84 lb
  • Range length
    2 (high) m
    6.56 (high) ft
  • Average length
    1 m
    3.28 ft

Re­pro­duc­tion

Males and fe­males are sex­u­ally ma­ture in their first year, usu­ally by 4-5 months old. Spawn­ing can occur at body lengths of 20 cm. Fe­males may spawn two to three times per year, and pro­duce be­tween 80,000 and 1,000,000 eggs per event.

In wa­ters above 34° C, lar­vae are found all year, with greater num­bers de­tected in spring and fall. In one study, sev­enty per­cent of the youngest lar­vae col­lected in the north­ern Gulf of Mex­ico were found at a depth greater than 180 me­ters. Spawn­ing oc­curs nor­mally in cap­tiv­ity, with 100,000 eggs per event. Prob­lems main­tain­ing salin­ity, food of ad­e­quate nu­tri­tional value and proper size, and dis­solved oxy­gen are re­spon­si­ble for lar­val mor­tal­ity rates of 20-40% (Lee, 1997). (Beard­s­ley, 1967; Ditty, et al., 1994; Lee, 1997)

  • Breeding interval
    Nutritional levels are likely to determine how frequently females can spawn.
  • Breeding season
    In warm waters, spawning can occur year round.
  • Range number of offspring
    80,000 to 1,000,000
  • Range age at sexual or reproductive maturity (female)
    12 (high) months
  • Average age at sexual or reproductive maturity (female)
    4-5 months
  • Range age at sexual or reproductive maturity (male)
    12 (high) months
  • Average age at sexual or reproductive maturity (male)
    4-5 months

Lifes­pan/Longevity

In cap­tiv­ity (aqua­cul­ture), dol­phin­fish have not been sus­tained for more than 18 months (Benetti, 1995). In the wild, they are be­lieved to live an av­er­age of 2 years, and a max­i­mum of 5 years (Beard­s­ley, 1967). (Beard­s­ley, 1967; Benetti, et al., 1995b; Ditty, et al., 1994)

  • Range lifespan
    Status: captivity
    18 (high) months
  • Typical lifespan
    Status: wild
    5 (high) years
  • Average lifespan
    Status: wild
    2 years
  • Average lifespan
    Status: captivity
    4 years
    AnAge

Be­hav­ior

Dol­phin are ac­tive gen­er­al­ist preda­tors which ex­pend high amounts of en­ergy in epipelagic re­gions for prey cap­ture. Due to their oxy­gen needs, dol­phin must swim con­tin­u­ously to ven­ti­late their gills. In order to achieve such high gas ex­change, dol­phin gills have a larger sur­face area than those of most other teleosts. This con­tributes to the higher en­ergy ex­pen­di­ture rel­a­tive to other teleosts. Dol­phin grow most rapidly in the wild, often reach­ing 1 meter in length and a mass of 8 kilo­grams at the end of the first year. How­ever, in cap­tiv­ity (aqua­cul­ture), dol­phin grow more slowly and have less stream­lined bod­ies. This is at­trib­uted to re­duced swim­ming due to small tanks and high pop­u­la­tion den­sity (Benetti, et al. 1995).

In­traspecies can­ni­bal­ism has been ob­served in some mem­bers (Mas­suti, et al. 1998).

Com­mu­ni­ca­tion and Per­cep­tion

Food Habits

Dol­phin ob­served in the west­ern Mediter­ranean are vi­sual gen­er­al­ist preda­tors, and hence feed pri­mar­ily dur­ing the day, when ad­e­quate sun­light is avail­able. They feed on teleosts, cephalopods, and crus­taceans, with a pos­i­tive cor­re­la­tion be­tween dol­phin size and prey size (Mas­suti, et al. 1998).

In cap­tiv­ity, dol­phin fed a sim­i­lar diet to that found in the wild (fish, squid, etc.) grow more slowly than those in the wild, but more rapidly than those fed with pro­tein-rich food pel­lets in cap­tiv­ity (Benetti, 1995).

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

C. hip­pu­rus is one of the most pop­u­lar sport­fish glob­ally. Be­cause it is prized for its meat as well, it is har­vested com­mer­cially both in the wild and via aqua­cul­ture

(Benetti, 1995).

Dol­phin grows rapidly in cap­tiv­ity, with low mor­tal­ity, which has al­lowed for hatch­eries and farms through­out the world (Mor­gan, et al. 1996; Lee, 1997).

Con­ser­va­tion Sta­tus

Other Com­ments

Due to re­cent ad­vance­ments in lar­val rear­ing via pro­longed re­search, dol­phin aqua­cul­ture pre­sents a po­ten­tially lu­cra­tive and abun­dant source of food for hu­mans, and re­duces the chance of com­mer­cial and sport over­fish­ing in the wild. (Lee, 1997)

Con­trib­u­tors

William Fink (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

Joshua Bost­wick (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

Atlantic Ocean

the body of water between Africa, Europe, the southern ocean (above 60 degrees south latitude), and the western hemisphere. It is the second largest ocean in the world after the Pacific Ocean.

World Map

Neotropical

living in the southern part of the New World. In other words, Central and South America.

World Map

Pacific Ocean

body of water between the southern ocean (above 60 degrees south latitude), Australia, Asia, and the western hemisphere. This is the world's largest ocean, covering about 28% of the world's surface.

World Map

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

chemical

uses smells or other chemicals to communicate

coastal

the nearshore aquatic habitats near a coast, or shoreline.

ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

external fertilization

fertilization takes place outside the female's body

fertilization

union of egg and spermatozoan

heterothermic

having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

motile

having the capacity to move from one place to another.

natatorial

specialized for swimming

native range

the area in which the animal is naturally found, the region in which it is endemic.

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

pelagic

An aquatic biome consisting of the open ocean, far from land, does not include sea bottom (benthic zone).

saltwater or marine

mainly lives in oceans, seas, or other bodies of salt water.

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

year-round breeding

breeding takes place throughout the year

Ref­er­ences

Beard­s­ley, G. 1967. Age, Growth, and Re­pro­duc­tion of the Dol­phin, Coryphaena hip­pu­rus, in the Straits of Florida.. Copeia, 1967: 441-451.

Benetti, D., R. Brill, S. Kraul. 1995. The stan­dard meta­bolic rate of dol­phin fish.. Jour­nal of Fish Bi­ol­ogy, 46(6): 987-996.

Benetti, D., E. Iver­son, A. Os­trowski. 1995. Growth rates of cap­tive dol­phin, Coryphaena hip­pu­rus, in Hawaii.. Fish­ery Bul­letin, 93(1): 152-157.

Ditty, J., R. Shaw, C. Grimes, J. Cope. 1994. Lar­val de­vel­op­ment, dis­tri­b­u­tion, and abun­dance of com­mon dol­phin, Coryphaena hip­pu­rus, and pom­pano dol­phin, C. eq­ui­selis (fam­ily: Coryphaenidae), in the north­ern Gulf of Mex­ico.. Fish­ery Bul­letin, 92(2): 275-291.

Lee, C. 1997. Ma­rine fin­fish hatch­ery tech­nol­ogy in the USA – sta­tus and fu­ture.. Hy­dro­bi­olo­gia, 358(1-3): 45-54.

Mas­suti, E., S. Deud­ero, P. Sanchez, B. Morales-Nin. 1998. Diet and feed­ing of dol­phin (Coryphaena hip­pu­rus) in west­ern Mediter­ranean wa­ters.. Bul­letin of Ma­rine Sci­ence, 63(2): 329-341.

Mor­gan, J., S. Bal­fry, M. Vi­jayan, G. Iwama. 1996. Phys­i­o­log­i­cal re­sponses to hy­pos­aline ex­po­sure and han­dling and con­fine­ment stress in ju­ve­nile dol­phin (mahimahi: Coryphanea hip­pu­rus).. Cana­dian Jour­nal of Fish­eries and Aquatic Sci­ences, 53(8): 1736-1740.

Palko, B., G. Beard­s­ley, W. Richards. 1982. Syn­op­sis of the bi­o­log­i­cal data on dol­phin­fishes, Coryphaena hip­pu­rus and Coryphaena eq­ui­selis. NMFS Circ. 443: NOAA Tech. Rep..

Pot­thoff, T. 1980. De­vel­op­ment and struc­ture of fins and fin sup­ports in dol­phin fishes. Fish­ery Bul­letin, 78(2): 277-312.

Quigley, D., K. Flan­nery. 1996. Com­mon dol­phin-fish Coryphanea hip­pu­rus L. in Irish and other north-. Irish Nat­u­ral­ists’ Jour­nal, 25(7): 260-263.