Pacific ocean perch

Pacific ocean perch
Sebastes alutus
Scientific classification
Kingdom:	Animalia
Phylum:	Chordata
Class:	Actinopterygii
Order:	Scorpaeniformes
Family:	Sebastidae
Genus:	Sebastes
Species:	S. alutus
Binomial name
Sebastes alutus (C. H. Gilbert, 1890)

A 40 ton catch of Pacific ocean perch about to come on board

Rockfish eyes can bulge as a result of being brought up from great depths

The Pacific ocean perch (Sebastes alutus), also known as the Pacific rockfish, Rose fish, Red bream or Red perch has a wide distribution in the North Pacific from southern California around the Pacific rim to northern Honshū, Japan, including the Bering Sea. The species appears to be most abundant in northern British Columbia, the Gulf of Alaska, and the Aleutian Islands (Allen and Smith 1988).

Habitat and migration

Adults are found primarily offshore on the outer continental shelf and the upper continental slope in depths 150–420 m. Seasonal differences in depth distribution have been noted by many investigators. In the summer, adults inhabit shallower depths, especially those between 150 and 300 m. In the fall, the fish apparently migrate farther offshore to depths of ~300–420 m. They reside in these deeper depths until about May, when they return to their shallower summer distribution (Love et al. 2002).

This seasonal pattern is probably related to summer feeding and winter spawning. Although small numbers of Pacific ocean perch are dispersed throughout their preferred depth range on the continental shelf and slope, most of the population occurs in patchy, localized aggregations (Hanselman et al. 2001). Pacific ocean perch are generally considered to be semi-demersal but there can at times be a significant pelagic component to their distribution. Pacific ocean perch often move off-bottom at night to feed, apparently following diel euphausiid migrations. Commercial fishing data in the Gulf of Alaska since 1995 show that pelagic trawls fished off-bottom have accounted for as much as 20% of the annual harvest of this species.

Life history

There is much uncertainty about the life history of Pacific ocean perch, although generally more is known than for other rockfish species (Kendall and Lenarz 1986). The species appears to be viviparous (the eggs develop internally and receive at least some nourishment from the mother), with internal fertilization and the release of live young. Insemination occurs in the fall, and sperm are retained within the female until fertilization takes place ~2 months later. The eggs hatch internally, and parturition (release of larvae) occurs in April–May.

Information on early life history is very sparse, especially for the first year of life. Pacific ocean perch larvae are thought to be pelagic and drift with the current, and oceanic conditions may sometimes cause advection to suboptimal areas (Ainley et al. 1993) resulting in high recruitment variability. However, larval studies of rockfish have been hindered by difficulties in species identification since many larval rockfish species share the same morphological characteristics (Kendall 2000). Genetic techniques using allozymes (Seeb and Kendall 1991) and mitochondrial DNA (Li 2004) are capable of identifying larvae and juveniles to species, but are expensive and time-consuming.

Post-larval and early young-of-the-year Pacific ocean perch have been positively identified in offshore, surface waters of the GOA (Gharrett et al. 2002), which suggests this may be the preferred habitat of this life stage. Transformation to a demersal existence may take place within the first year (Carlson and Haight 1976). Small juveniles probably reside inshore in very rocky, high relief areas, and by age 3 begin to migrate to deeper offshore waters of the continental shelf (Carlson and Straty 1981). As they grow, they continue to migrate deeper, eventually reaching the continental slope, where they attain adulthood.

Ecology

Pacific ocean perch are mostly planktivorous (Carlson and Haight 1976, Yang 1993, 1996, Yang and Nelson 2000, Yang 2003). In a sample of 600 juvenile perch stomachs, Carlson and Haight (1976) found that juveniles fed on an equal mix of calanoid copepods and euphausiids. Larger juveniles and adults fed primarily on euphausiids, and to a lesser degree, copepods, amphipods and mysids (Yang and Nelson 2000). In the Aleutian Islands, myctophids have increasingly comprised a substantial portion of the Pacific ocean perch diet, which also compete for euphausiid prey (Yang 2003). It has been suggested that Pacific ocean perch and walleye pollock compete for the same euphausiid prey. Consequently, the large removals of Pacific ocean perch by foreign fishermen in the Gulf of Alaska in the 1960s may have allowed walleye pollock stocks to greatly expand in abundance.

Predators of adult Pacific ocean perch are likely sablefish, Pacific halibut, and sperm whales (Major and Shippen 1970). Juveniles are consumed by seabirds (Ainley et al. 1993), other rockfish (Hobson et al. 2001), salmon, lingcod, and other large demersal fish.

Population

Pacific ocean perch is a very slow growing species, with a low rate of natural mortality (estimated at 0.06), a relatively old age at 50% maturity (10.5 years for females in the Gulf of Alaska), and a very old maximum age of 98 years in Alaska (84 years maximum age in the Gulf of Alaska) (Hanselman et al. 2003). Age at 50% recruitment to the commercial fishery has been estimated to be between 7 and 8 years in the Gulf of Alaska. Despite their viviparous nature, the fish is relatively fecund with number of eggs/female in Alaska ranging from 10,000-300,000, depending upon size of the fish (Leaman 1991).

The evolutionary strategy of spreading reproductive output over many years is a way of ensuring some reproductive success through long periods of poor larval survival (Leaman and Beamish 1984). Fishing generally selectively removes the older and faster-growing portion of the population. If there is a distinct evolutionary advantage of retaining the oldest fish in the population, either because of higher fecundity or because of different spawning times, age-truncation could be ruinous to a population with highly episodic recruitment like rockfish (Longhurst 2002). Recent work on black rockfish (Sebastes melanops) has shown that larval survival may be dramatically higher from older female spawners (Berkeley et al. 2004, Bobko and Berkeley 2004). The black rockfish population has shown a distinct downward trend in age-structure in recent fishery samples off the West Coast of North America, raising concerns about whether these are general results for most rockfish. De Bruin et al. (2004) examined Pacific ocean perch (S. alutus) and rougheye rockfish (S. aleutianus) for senescence in reproductive activity of older fish and found that oogenesis continues at advanced ages. Leaman (1991) showed that older individuals have slightly higher egg dry weight than their middle-aged counterparts. Such relationships have not yet been determined to exist for Pacific ocean perch or other rockfish in Alaska.

Few studies have been conducted on the stock structure of Pacific ocean perch. Based on allozyme variation, Seeb and Gunderson (1988) concluded that Pacific ocean perch are genetically quite similar throughout their range, and genetic exchange may be the result of dispersion at early life stages. In contrast, preliminary analysis using mitochondrial DNA techniques suggest that genetically distinct populations of Pacific ocean perch exist (A. J. Gharrett pers. commun., University of Alaska Fairbanks, October 2000). Withler et al. (2001) found distinct genetic populations on a small scale in British Columbia. Currently, genetic studies are underway that should clarify the genetic stock structure of Pacific ocean perch.

The fishery for Pacific ocean perch developed nearly synchronously from the U.S. West Coast to the Bering Sea. The Gulf of Alaska fishing history captures a typical catch history: A Pacific ocean perch trawl fishery by the U.S.S.R. and Japan began in the Gulf of Alaska in the early 1960s. This fishery developed rapidly, with massive efforts by the Soviet and Japanese fleets. Catches peaked in 1965, when a total of nearly 350,000 metric tons (t) was caught. This apparent overfishing resulted in a precipitous decline in catches in the late 1960s. Catches continued to decline in the 1970s, and by 1978 catches were only 8,000 t. Foreign fishing dominated the fishery from 1977 to 1984, and catches generally declined during this period. Most of the catch was taken by Japan (Carlson et al. 1986). Catches reached a minimum in 1985, after foreign trawling in the Gulf of Alaska was prohibited.

Conservative management measures, an excellent observer program, and perhaps higher productivity in Alaska have allowed the stock to recover to a level to allow about 26,000 tons per annum. U.S. West Coast stocks are beginning to show signs of recovery, but are still in the process of rebuilding.

Works cited

Other references

v t e Principal commercial fishery species groups Wild Large pelagic fish Mackerel Salmon Saury Shark Swordfish Tuna albacore bigeye Atlantic bluefin Pacific bluefin southern bluefin skipjack yellowfin Forage fish Anchovy Capelin Herring Ilish Menhaden Sardines Shad Sprat european Demersal fish Catfish Cod Atlantic Pacific Flatfish flounder halibut plaice sole turbot Haddock Mullet Orange roughy Pollock Rockfish Smelt-whitings Toothfish Freshwater fish Carp Sturgeon Tilapia Trout Other wild fish Eel Whitebait more... Crustaceans Crab Krill Lobster Shrimp more... Molluscs Abalone Mussels Octopus Oysters Scallops Squid more... Echinoderms Sea cucumbers Sea urchin more... Farmed Carp bighead common crucian grass silver Catfish Freshwater prawns Gilt-head bream Mussels Oysters Salmon Atlantic salmon trout coho chinook Scallops Seaweed Shrimp Tilapia Commercial fishing World fish production Fishing topics Fisheries glossary