Theragra chalcogramma (Alaska pollock) occupies a wide geographic range and is found in a polar climate across the northern Pacific Ocean, from 68° north to 34° north, and from 129° east to 120° west (Kooka 1998). Alaska pollock inhabit a broad niche spanning the North Pacific, from the eastern Paleartic region to the western Neartic. North American populations lie along the west coast from northern California to northwest Alaska with major populations located southeast of Alaska and Canada and in the western-central Gulf of Alaska. Alaska pollock populations span the coastline of West Asia to South-West Asia and South Asia with the largest populations concentrated in the northwestern Bering Sea, the western Bering Sea, eastern Kamchatka, and the northern Sea of Okhotsk. (Bailey, et al., 1999; Kooka, 1998)
Theragra chalcogramma is a saltwater fish that thrives in seas, oceans, and gulfs. It is broadly distributed with greater populations existing in the outer shelf and slope regions of oceanic waters. These fish, semi-demersal in some regions and pelagic in others (due to feeding on a variety of pelagic and demersal prey), are able to survive in large estuaries, coastal areas, and open basins. Alaska pollock are limited to northern regions reflecting this species' limited temperature tolerance. They can only withstand a range of ten to twelve degrees Celsius (Bailey 1999). Common trends exhibit an age-dependent depth distribution. Fish less than one year old live throughout the water column, one-year-olds live at bottom trawls, two- to three-year-olds live higher in the column, and fish at least four years old display demersal behavior. The thermal range of these fish decreases with age. Younger fish have a greater range of temperature tolerance than older fish, which remain at lower depths where the temperature is a constant one to six degrees Celsius (Avdeev 2001). (Avdeev, G.V and Avdeev, 2001; Bailey, et al., 1999)
Theragra chalcogramma has an olive-green belly. Its dorsal side displays a gradually darkening color scheme from the bottom to the top, eventually fading to a dark brown. This fish exhibits characteristic blotches all over its entire body, which is slender with a large head. The head consists of various lateral pores, large eyes, and a protruding lower jaw which lacks a barbel (Bailey 1999). Theragra chalcogramma can be recognized by its two anal fins, three widely dispersed fins on its back, and outstretched pelvic fins. The fins are all a dark grey to black color. A lateral line runs across the fish to its caudal fin. At three to five years old, the average length of this fish is 30.5 centimeters (Harmann 2005). By the time it reaches ages of eight to twelve years, the average length is about 61 centimeters. The maximum length of T. chalcogramma is 91 centimeters. Weights of this fish range from 600 grams to 800. The maximum weight was recorded at 1400 grams (Cohen 1990). (Bailey, et al., 1999; Cohen, et al., 1990; Harmann, 2005)
Newly fertilized pelagic eggs of Theragra chalcogramma are approximately 3.4 mm in diameter. The eggs hatch in approximately 28 days at a temperature of three degrees Celcius. The length of each larva when it settles out is 3.8 to 5.1 centimeters (Love 1996). The larval developmental stage is considered complete within approximately 50 days. Females grow at the same rate as, or slightly faster than, males. Immature fish swim towards the surface at night to capture prey. The pre-spawning stage begins at age 2 years. Female T. chalcogramma reach maturity at three to four years at an average length of 36 centimeters, while males mature at ages four to five years (Bailey 1999). (Bailey, et al., 1999; Love, 1996)
These fish spawn in large groups. The mating system of Theragra chalcogramma consists of females releasing their eggs and then males randomly fertilizing them (Love 1996). Females are referred to as batch spawners that release eggs every few days for one month per year. (Cohen, et al., 1990; Love, 1996)
Spawning of Theragra chalcogramma occurs in water depths of 90 to 200 meters. Spawning, which occurs for an entire month, is annual and the peak spawning season fluctuates from region to region. Early spawning, in the months of February, March and April, occurs in the Bering Sea. Later spawning, in the months of April, May, and June, occurs further inward over the continental slope and shelf. Spawning fish (three- to four-year-old females and four- to five-year-old males) and pre-spawning fish (two-year-old females) swim high to mid-water in dense schools. The amount of eggs that each female holds is proportional to her body size. Females of approximately 60 centimeters produce 500,000 to 600,000 eggs while females with lengths of 40 to 45 centimeters produce about one third of that. The largest of females have been known to produce up to one million eggs (Harmann 2005). Theragra chalcogramma eggs, which are transported by currents, are planktonic (Love 1996). The eggs take anywhere from 9 to 28 days to hatch. (Love, 1996; Harmann, 2005; Love, 1996)
The mortality coefficient for Theragra chalcogramma is 0.3 on the eastern Bering Sea shelf (0.3 implying that that the annual natural morality rate is 30%) and 0.2 on the Aleutian Basin. Theragra chalcogramma usually lives from 12 to 16 years. The oldest T. chalcogramma ever reported was 31 years old (Bailey 1999). (Bailey, et al., 1999)
Theragra chalcogramma is a mobile species that is social and travels in schools. Dense schools of Theragra chalcogramma form during the spawning season. Depth, temperature, and cold fronts contribute to the vertical distribution of juvenile Alaska pollock. These factors also effect the horizontal distribution of adult schools, which usually stay within a range of 0 to 2 degrees Celcius. At night, juvenile fish can be found near the surface, indicating their distinctive eating pattern. This is called vertical migration, and occurs when fish travel upward in the water column to the surface to attain a larger population of potential prey. Schooling cohesion decreases at night as well as times of limited food. (Harmann, 2005; Harmann, 2005; Avdeev, G.V and Avdeev, 2001; Bailey, et al., 1999; Harmann, 2005)
No information on the home range of Theragra chalcogramma could be found.
Limited information pertaining to the communication and perception of Theragra chalcogramma exists. Most schooling fish, however, use visual cues for schooling and feeding (Bailey 1999). (Bailey, et al., 1999)
Theragra chalcogramma feeds on both fish and invertebrates (Bailey 1999). The diet of this fish varies by developmental stage, season, and body size. Larvae tend to consume zooplankton such as larval copepods, while older T. chalcogramma tend to eat larger food items such as adult Acartia and Pseudocalanus. In winter, adult pollock feed mostly on fishes and euphausiid krill. In spring, T. chalcogramma feed on Appendicularia. In summer, the diet consists of euphausiids and copepods and in autumn, they feed on mainly euphausiids (Kooka 1998). Large T. chalcogramma have a diet rich in small pollock (specifically in the eastern Bering Sea) and shrimp. In areas where the juvenile population is extremely large, such as in the eastern Bering Sea, cannabalistic adults prey on the juveniles. Smaller-sized individuals are more likely to consume copepods and euphausiids (Avdeev 2001). (Avdeev, G.V and Avdeev, 2001; Bailey, et al., 1999; Kooka, 1998)
Theragra chalcogramma larvae are preyed on by northern rockfish, polka-dot snailfish, and atka mackeral. One-year-olds are preyed on by greenland turbot, plain sculpin, and arrowtooth flounder. Those that are two years old are hunted by greenland turbot, bigmouth sculpin, sablefish, pacific cod, plain sculpin, pacific halibut, and great sculpin. Adult T. chalcogramma fall prey to yellow irish lords and plain sculpin (Cohen 1990; Kooka 1998). In the Gulf of Alaska, T. chalcogramma is the primary prey of stellar sea lions (Cohen 1999). (Cohen, et al., 1990; Kooka, 1998; Love, 1996)
Predator-prey interactions for T. chalcogramma fluctuate with seasonal conditions. One-year-old pollock occupy different areas depending on temperature. This change in local abundance affects the annual populations of other species in the region.
When infected with the parasitic copepod Haemobaphes diceraus, there is a decrease in the body weight of T. chalcogramma as well as an increase in the weight of its spleen. If T. chalcogramma is infected during the juvenile stage of development, it suffers from delayed maturity, and if it is infected as an adult, it experiences a decrease in reproductive success (Bailey 1999). (Avdeev, G.V and Avdeev, 2001; Bailey, et al., 1999)
This species is a valuable fish for fisheries on the Russian, Japanese, and Korean coasts. The fish is sold frozen, as fillets, fish sticks, surimi, and roe in Japan (Love 1996). The desire for this fish has gone up in recent years; however, it still lacks appreciation on the North Californian coast where its abundance is high. In addition to being used for food, it is also utilized for fish meal and industrial products. (Love, 1996)
This species is not threatened and is not listed on the 2004 IUCN Red List of Threatened Species nor is it listed as endangered by the U.S. Fish and Wildlife Service. The most important site of reproduction for this species, the Shelikof Strait in the Gulf of Alaska, has an annual period of time in which fishing is prohibited. This enforced fishing restriction was put in place to prevent potential decreases in this species due to this region having such a large T. chalcogramma density during spawning season (Bailey 1999). (Bailey, et al., 1999; Bailey, et al., 1999)
Allison Poor (editor), University of Michigan-Ann Arbor.
Parisa Ijadi-Maghsoodi (author), University of Michigan-Ann Arbor, Kevin Wehrly (editor, instructor), University of Michigan-Ann Arbor.
living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.
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.
living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.
Referring to an animal that lives on or near the bottom of a body of water. Also an aquatic biome consisting of the ocean bottom below the pelagic and coastal zones. Bottom habitats in the very deepest oceans (below 9000 m) are sometimes referred to as the abyssal zone. see also oceanic vent.
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
the nearshore aquatic habitats near a coast, or shoreline.
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
an area where a freshwater river meets the ocean and tidal influences result in fluctuations in salinity.
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.
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).
a species whose presence or absence strongly affects populations of other species in that area such that the extirpation of the keystone species in an area will result in the ultimate extirpation of many more species in that area (Example: sea otter).
having the capacity to move from one place to another.
specialized for swimming
the area in which the animal is naturally found, the region in which it is endemic.
active during the night
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
the regions of the earth that surround the north and south poles, from the north pole to 60 degrees north and from the south pole to 60 degrees south.
the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.
mainly lives in oceans, seas, or other bodies of salt water.
breeding is confined to a particular season
reproduction that includes combining the genetic contribution of two individuals, a male and a female
associates with others of its species; forms social groups.
uses touch to communicate
uses sight to communicate
animal constituent of plankton; mainly small crustaceans and fish larvae. (Compare to phytoplankton.)
Avdeev, G.V, G., E. Avdeev. 2001. Patogenic [pathogenic] influence rendered by parasitic copepod Haemobaphes diceraus on Alaska pollock. Zoological Record Plus, 128(1): 287-292, 336, 342.
Bailey, K., D. Powers, J. Quattro, G. Villa, J. Traynor, G. Walters. 1999. Population Ecology and Structural Dyamics of Walleye Pollock. Pp. 581-590 in T Loughlin, K Ohtani, eds. Dynamics of the Bering Sea. Fairbanks, Alaska: University of Alaska Sea Grant.
Cohen, D., T. Inada, T. Iwamoto, N. Scialabba. 1990. "Theraga chalcogramma" (On-line). Accessed October 12, 2005 at http://www.fishbase.org/Summary/SpeciesSummary.php?id=318.
Harmann, A. 2005. "A Biophysical Model of Shelikof Strait" (On-line). Accessed October 16, 2005 at http://www.pmel.noaa.gov/foci/spem-ibm.html.
Kooka, K. 1998. Vertical distribution and prey of walleye pollock in the northern Japan sea. Fisheries Sciecne, 64 (5): 686-693.
Love, M. 1996. Probably more than you want to know about the fishes of the Pacific coast.. Sante Fe, California: Really Big Press.