Makaira nigricansBlue Marlin(Also: Cuban black marlin)

Geographic Range

Makaira nigricans is distributed mainly in the tropical and temperate waters of the Atlantic, Pacific, and Indian Oceans. It is the most tropical of all billfishes.

In the Atlantic Ocean, its range extends to around 40-45N in the North Atlantic and to 40S in the western Atlantic, 30S in the central South Atlantic and 35S in the eastern south Atlantic, but is absent from the Mediterranean Sea. In the Pacific, its range extends to about 45N in the western North Pacific, 35N in the eastern North Pacific, 35S in the western South Pacific, and 25S in the eastern South Pacific. In the Indian Ocean, its range extends to 45S in the southwestern Indian Ocean and 35S in the southeastern Indian Ocean.

Larvae are found extensively in the tropical and subtropical waters of the western and central Pacific Ocean, south of Maldives Islands, around the Mascalene Islands, and off the south coasts of Java and Sumatra in the Indian Ocean. In the western central Atlantic, larvae are found off Georgia, North Carolina, Florida, Jamaica, Bahamas, Arecibo, and also off Brazil in the southwest Atlantic. (Nakamura, 1985)


Makaira nigricans is an epipelagic and oceanic species. It is the most oceanic of all istiophorids, usually remaining far from land except where the continental shelf is narrow. It can be found in waters with surface temperatures of 22-31C, but it prefers the warm mixed layer above the thermocline, and spends the majority of its time in the uniformly warm near-surface waters from 25-27C. It shows preference for blue waters, at least in the northern Gulf of Mexico. (Block, et al., 1992a; Block, et al., 1992b; deSylva and Breder, 1997; Nakamura, 1985)

Physical Description

Makaira nigricans possesses a long bill that is very stout and round in cross section, with a conspicuous elevated nape (the part of neck posterior to the head). Small, file-like teeth line both jaws and the roof of its mouth. It has two dorsal fins, and two anal fins. The body is densely covered with elongated, thick bony scales, each with mostly 1 or 2, sometimes 3 posterior points. Body coloration is blue black on the dorsal side and silvery white on the ventral side, with approximately 15 rows of pale cobalt-colored strips made up of round dots and/or narrow bars running down both sides of the body. The first dorsal fin is blackish or dark blue, while the other fins are usually dark brown, sometimes tinged with dark blue. The bases of the anal fins are tinged silvery white.

When swimming rapidly, M. nigricans can fold its first dorsal, first anal, and pectoral fins down into fin grooves on the body to increase streamlining. In contrast, the pectoral fins of its near relative, Makaira indica (black marlin), are rigid and cannot be folded back against its body.

Makaira nigricans is one of the largest fish in the world. Weight averages between 126 kg and 181 kg. Length averages from about 200 to 300 cm lower jaw fork length (LJFL), which is measured from the tip of the lower jaw to the posterior margin of the middle caudal ray. The largest male recorded in the scientific literature is 170.3 kg, 263.1 cm LJFT, while the largest female is 748.0kg, 445.8 cm LJFT.

Sexual dimorphism is exhibited in weight, where the females are typically heavier than males. Weight dimorphism begins at 140 cm LJFL when the females start growing at a faster rate than the males. Females usually grow to at least 540 kg, while males seldom exceed 160kg. (Nakamura, 1985; Wilson, et al., 1991)

  • Sexual Dimorphism
  • female larger
  • Range mass
    748 (high) kg
    1647.58 (high) lb
  • Average mass
    126-181 kg
  • Range length
    455.8 (high) cm
    179.45 (high) in
  • Average length
    200-300 cm


In terms of absolute growth rate, M. nigricans is one of the most rapidly growing teleosts during the early stages. The maximum growth rate of larvae can reach ~16mm/day. (Prince, et al., 1991)


The spawning season extends from July through October in the North Atlantic. In the South Atlantic, M. nigricans exhibits fall spawning when the sea surface temperature is at 28C. In the Pacific Ocean, spawning occurs from December to January during the southern hemisphere’s summer. Females can spawn up to four times during the reproductive season, while males can spawn year round.

Sexual maturity is reached at 2-4 years of age. Females reach sexual maturity at 120kg or below. The smallest mature female recorded weighs 45kg. Fecundity of a female at 124 kg is estimated to be 7 million eggs, and 10.9 million eggs for a female of 147kg. Eggs are spherical, transparent, white to yellow in color, and around 1mm in diameter. (Bartlett and Haedrich, 1968; deSylva and Breder, 1997; Erdman, 1968; Kume and Joseph, 1969; Nakamura, 1985)

  • Breeding season
    varies depending on geographic location
  • Average time to hatching
    1 weeks
  • Average age at sexual or reproductive maturity (female)
    2-4 years
  • Average age at sexual or reproductive maturity (male)
    2-4 years

The eggs are bouyant in the water and drift until hatching with no parental care. (Nakamura, 1985)

  • Parental Investment
  • no parental involvement
  • pre-fertilization
    • provisioning
    • protecting
      • female


The maximum lifespan of females is estimated to be at least 27 years, while males are estimated to live a maximum of 18 years. (Hill, et al., 1989)

  • Typical lifespan
    Status: wild
    20 to 30 years
  • Average lifespan
    Status: wild
    20-30 years


Makaira nigricans is rare and primarily solitary, in contrast to the other schooling scrombids. It is highly migratory, and has exhibited transequatorial and transatlantic movements. Evidence from The Cooperative Game Fish Tagging Program in the western North Atlantic demonstrated two-way, seasonal movements between the Caribbean Islands, Venezuela and the Bahamas, and at least one-way travel from St. Thomas at the U.S. Virgin Island to the Ivory Coast of West Africa (7,000 km). Makaira nigricans also engages in a daily cycle of vertical migration, swimming deeper in the day and closer to the surface at night.

Makaira nigricans is a subcarangiform swimmer that propels itself with its caudal fin and displaces water with side to side undulatory movements, similar to a shark. It follows a straight or slightly curving course when swimming. Typically, it travels at low speeds of around 2-3km/h for long periods, which are punctuated by short bursts of rapid speed associated with descents down the water column. The fastest speed measured by a speedmometer is 225cm/s, though it has been observed to attack fish bait trawled at 800cm/s. As a continuous swimmer, it can cover 40-70 km in a day. (Block, et al., 1992a; Block, et al., 1992b; Hebrank, et al., 1990; Holland, et al., 1990; Witzell and Scott, 1990)

Communication and Perception

Food Habits

Makaira nigricans is an apex predator. Often, it approaches a school of fish or invertebrates at full speed, slashes through with its bill, then returns to devour the stunned or dead prey. It forages mostly in the near-surface waters, but the presence of benthic and demersal species in its stomach indicates it also feeds near the bottom. It consumes a large variety of prey species of different sizes and morphology from various trophic levels. But it also disproportionately targets a few species. This indicates that M. nigricans is a specialized but opportunistic feeder, a foraging mode suited to the warm water oceans where food is unevenly distributed.

The numbers and types of species consumed vary, depending on the location and season. For instance, M. nigricans feeds mainly on bullet mackerel (Auxis spp.) off the coast of Mexico, and on shipjack tuna (Kutsuwonus pelamis) in the central Pacific. Fish is the most frequent prey, and can constitute up to 86% of the total volume of food consumed by M. nigricans in Hawaii. Scrombidae, especially tuna-like species, are consistently the most important prey items, among which shipjack tuna (K. pelamis) and frigate mackerel (Auxis thazard) are the most common. Tuna-like species are abundant, co-occur over the geographic range and epipelagic habitat of M. nigricans and are of appropriate size as prey for an adult blue marlin.

Makaira nigricans also feeds on a small amount of inshore juvenile fish, among which Balistidae and Acanthuridae are more common. Among the cephalopods that are consumed, squids from the family Ommastrephidae are commonly consumed, along with many other kinds of squids. (Abitia-Cardenas, et al., 2000; Baker, 1966; Block, et al., 1992b; Brock, 1984; Erdman, 1962; Nakamura, 1985; Royce, 1957; Strasburg, 1970)

  • Animal Foods
  • fish
  • mollusks
  • aquatic crustaceans


  • Known Predators
    • great white sharks (Carcharodon carcharias)
    • shortfin mako (Isurus oxyrhinchus)
    • capsalid monogenean parasites (Tristomella laevis)
    • parasitic copepods (Penella makaira)

Ecosystem Roles

The blue marlin occupies a high trophic level, feeding on pelegic and benthic organisms in the ecosystem of the open ocean.

(Gardieff, 2003)

Economic Importance for Humans: Positive

Makaira nigricans is usually caught as bycatch in tuna longline fisheries but has some commercial value throughout the world. In 2000, blue marlin landings totaled 25717 metric tons in the Pacific and 3064 metric tons in the Atlantic. The countries with the largest landings are Taiwan, China (13618 mt) and Japan (7899 mt). Other countries with blue marlin captures include Ghana, Brazil, Cote divoire, and South Korea. Blue marlin flesh is of excellent quality. It is especially valuable in Japan, where flesh with high fat content is used raw for sashimi.

Due to its rarity, large size, legendary speed, and powerful aerobics on rod and reel, M. nigricans is a popular and prestigious catch for recreational fishermen. In fact, an entire multi-million dollar industry has evolved around this “rare event” species. Sport fisheries are especially developed in the U.S., Venezuela, Bahamas, Brazil, the Caribbean, and along the coast of West Africa. (FAO, 2002; ICCAT, October 2002; Witzell and Scott, 1990)

Conservation Status

The blue marlin stock in the Atlantic has probably been overfished for the last 10-15 years. Its maximum sustained yield is estimated to be 2000 metric tons, so the stock is being depleted faster that it can replenish itself at landings of 3064 metric tons in 2000. The predominant blue marlin landings occur as bycatch in offshore longline fisheries that target tropical and temperate tunas by fishing shallow, and to a lesser degree in offshore longline fisheries and drift nets targeting swordfish and bigeye tuna by fishing deep.

Due to their migratory nature, wide geographic range, and multinational fishing pressure, it is difficult to manage and set up regulations to protect the blue marlin stock.

The International Commission for the Conservation of Atlantic Tunas (ICCAT) is a major international organization with 32 contracting countries aiming to conserve tunas and tuna-like species in the Atlantic Ocean and adjacent seas. Makaira nigricans is one of the 30 species of direct concern to ICCAT. The Commission has recommended that the blue marlin landings of pelagic longlines and purse seine vessels be reduced to at most 50% of the 1996 or 1999 level, whichever is greater. In the US, the NMFS has imposed a size limit of 251cm LJFL on the recreational blue marlin catch, and has prohibited commercial fishermen from fishing, taking, or retaining blue marlin. (Block, et al., 1992a; FAO, 2002; ICCAT, October 2002)

Other Comments

There is an ongoing disagreement on whether blue marlin populations in the Atlantic and Indo-pacific regions are distinct species. Some consider them to be a single pantropical species occurring in the Atlantic, Pacific and Indian Ocean. Others consider them to be two distinct species, namely the Atlantic blue marlin (Makaira nigricans) and Indo-Pacific blue marlin (Makaira mazara), due to their different lateral line patterns. Lateral line is a series of organs enclosed in tubular scales along the side of the body of a fish. Blue marlin in the Atlantic have a reticulate, complicated network of lateral line patterns, while Pacific blue marlin have single looped patterns. The presence of identical haplotypes in blue marlin samples from the Atlantic and Pacific suggests that they should be considered a single species.

Makaira nigricans is the giant monster the “old man” battled with for three days and nights non-stop in Ernest Hemingway’s classic “The Old Man and the Sea”. (Graves and McDowell, 1995; Nakamura, 1985)


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

Luana Tung (author), University of Michigan-Ann Arbor.


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

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.


an animal that mainly eats meat


uses smells or other chemicals to communicate

  1. active during the day, 2. lasting for one day.

humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.

external fertilization

fertilization takes place outside the female's body


union of egg and spermatozoan


A substance that provides both nutrients and energy to a living thing.


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.


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).


makes seasonal movements between breeding and wintering grounds


eats mollusks, members of Phylum Mollusca


having the capacity to move from one place to another.


specialized for swimming

native range

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


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


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


an animal that mainly eats fish

saltwater or marine

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

seasonal breeding

breeding is confined to a particular season


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


lives alone


uses touch to communicate


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).


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


Abitia-Cardenas, L., F. Galvan-Magaña, F. Gutierrez-Sanchez, J. Rodriguez-Romero, B. Aguilar-Palomino. 2000. Diet of blue marlin *Makaira mazara* off the coast of Cabo San Lucas, Baja California Sur, Mexico. Fisheries Research, 44: 95-100.

Baker, A. 1966. Food of marlins from New Zealand waters. Copeia, 4: 818-822.

Bartlett, M., R. Haedrich. 1968. Neuston nets and South Atlantic blue marlin (*Makaira nigricans*). Copeia, 1968: 469-474.

Block, B., D. Booth, F. Carey. 1992a. Depth and temperature of the blue marlin, *Makaira nigricans ,* observed by acoustic telemetry. Marine biology, 114: 175-183.

Block, B., D. Booth, F. Carey. 1992b. Direct measurement of swimming speeds and depth of blue marlin. Journal of Experimental Biology, 166: 267-284.

Brock, R. 1984. A contribution to the trophic biology of the blue marlin (*Makaira nigricans* Lacepede, 1802) in Hawaii. Pacific Science, 38: 141-149.

Erdman, D. 1968. Spawning cycles, sex ratio and weights of blue marlin off the coast of Puetro Rico and the Virgin Islands. Transactions of the American Fisheries Society, 97: 121-137.

Erdman, D. 1962. The sport fishery for blue marlin off Puerto Rico. Transactions of the American Fisheries Society, 91: 225-227.

FAO, 2002. FAO yearbook. Fishery Statistics. Vol. 90/1.. Rome: Agriculture and Food Organization of the United Nations.

Graves, J., J. McDowell. 1995. Inter-ocean genetic divergence of istiophorid billfishes. Marine biology, 122: 1179-1196.

Hebrank, J., J. Hebrank, J. Long, B. Block, S. Wainwright. 1990. Backbone mechanics of the blue marlin *Makaira nigricans* (Pisces, Istiophoridae). Journal of Experimental Biology, 148: 449-459.

Hill, K., G. Caillict, R. Radtke. 1989. A comparative analysis of growth zones in four calcified structures of Pacific blue marlin, *Makaira nigricans*. Fishery Bulletin, 87: 829-843.

Holland, K., R. Brill, R. Chang. 1990. Horizontal and vertical movements of Pacific blue marlin captured and released using sportfishing gear. Fishery Bulletin, 88: 397-402.

ICCAT, October 2002. "ICCAT Executive Summaries of Species Status Reports (Oct 2002)" (On-line). Accessed November 7, 2002 at

Kume, S., J. Joseph. 1969. Size composition of billfish caught by the Japanese longline fishery in the Pacific Ocean east of 130W. Bulletin of Far Sea Fishery Research Laboratory, 2: 115-161.

NMFS, "A Short Summary of the Recreational Fishing Regulations for Highly Migratory Species" (On-line). Accessed November 7, 2002 at

Nakamura, I. 1985. FAO species catalogue. Vol.5. Billfishes of the World. An annotated and illustrated catalogue of marlins, sailfishes, spearfishes and swordfishes known to date. Rome: United Nations Development Programme Food and Agriculture Organization of the United Nations.

Prince, E., D. Lee, J. Zweifel, E. Brothers. 1991. Estimating age and growth of young Atlantic blue marlin Makaira nigricans from otolith microstructure. Fishery Bulletin, 89: 441-459.

Royce, W. 1957. Observations on the spearfishes of the Central Pacific. Fishery Bulletin, 57: 497-554.

Strasburg, D. 1970. A report on the billfishes of the Central Pacific ocean. Bulletin of Marine Science, Bulletin of Marine Science: 575-604.

Wilson, C., J. Dean, E. Prince, D. Lee. 1991. An examination of sexual dimorphism in Atlantic and Pacific blue marlin using body weight, sagittae weight, and age estimates. Journal of Experimental Marine Biology and Ecology, 151: 209-225.

Witzell, W., E. Scott. 1990. Blue marlin, *Makaira nigricans* , movements in the western North Atlantic Ocean: Results of a cooperative game fish tagging program, 1954-88. Marine Fisheries Review, 52: 12-17.

deSylva, D., P. Breder. 1997. Reproduction, gonad histology, and spawning cycles of north Atlantic billfishes (Istiophoridae). Bulletin of Marine Science, 60: 668-698.