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^[jargon]. 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.

Commercial fishing

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. The U.S. West Coast stock was declared rebuilt in 2017 after 17 years in a rebuilding plan (PFMC 2017).

Works cited

Ainley, D.G.; Sydeman, W.J.; Parrish, R.H.; Lenarz, W.H. (1993). "Oceanic factors influencing distribution of young rockfish (Sebastes) in central California: A predator's perspective". CalCOFI Report. 34: 133–139. {{cite journal}}: Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)
Allen, M. J.; G. B. Smith (1988). "Atlas and zoogeography of common fishes in the Bering Sea and northeastern Pacific". NOAA Tech. Rept. NMFS. 66. U.S. Dep. Commer.: 151 p. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
Berkeley, S. A.; C. Chapman; S. M. Sogard (2004). "Maternal age as a determinant of larval growth and survival in a marine fish, Sebastes melanops". Ecology. 85 (5): 1258–1264. doi:10.1890/03-0706. {{cite journal}}: Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)
Bobko, S.J.; S.A. Berkeley (2004). "Maturity, ovarian cycle, fecundity, and age-specific parturition of black rockfish (Sebastes melanops)". Fisheries Bulletin. 102: 418–429. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
Carlson, H.R.; D.H. Ito; R.E. Haight; T.L. Rutecki; J.F. Karinen (1986). "Pacific ocean perch". In R.L. Major (ed.). Condition of groundfish resources of the Gulf of Alaska region as assessed in 1985. U.S. Dept. Commer., NOAA Tech. Memo. NMFS F/NWC-106. pp. 155–209. {{cite conference}}: Unknown parameter |booktitle= ignored (|book-title= suggested) (help); Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)
Carlson, H. R.; R. E. Haight (1976). "Juvenile life of Pacific ocean perch, Sebastes alutus, in coastal fiords of southeastern Alaska: their environment, growth, food habits, and schooling behavior". Trans. Am. Fish. Soc. 105 (2): 191–201. doi:10.1577/1548-8659(1976)105<191:JLOPOP>2.0.CO;2. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
Carlson, H. R.; R. R. Straty (1981). "Habitat and nursery grounds of Pacific rockfish, Sebastes spp., in rocky coastal areas of Southeastern Alaska". Mar. Fish. Rev. 43: 13–19. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
de Bruin, J.; R. Gosden; C. Finch; B. Leaman (2004). "Ovarian aging in two species of long-lived rockfish, sebastes aleutianus and S. alutus". Biol. Reprod. 71 (3): 1036–1042. doi:10.1095/biolreprod.103.019919. PMID 15151924. {{cite journal}}: Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)
Gharrett, A. J.; Z. Li; C. M. Kondzela; A. W. Kendall (2002). "Final report: species of rockfish (Sebastes spp.) collected during ABL-OCC cruises in the Gulf of Alaska in 1998-2002". (Unpubl. manuscr. available from the NMFS Auke Bay Laboratory, 11305 Glacier Hwy., Juneau AK 99801). {{cite journal}}: Cite journal requires |journal= (help); Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)
Hanselman, D.H.; T.J. Quinn II; C. Lunsford; J. Heifetz; D.M. Clausen (2001). "Spatial implications of adaptive cluster sampling on Gulf of Alaska rockfish". Proceedings of the 17th Lowell-Wakefield Symposium: Spatial Processes and Management of Marine Populations. Fairbanks, AK: Univ. Alaska Sea Grant Program. pp. 303–325. {{cite conference}}: Unknown parameter |booktitle= ignored (|book-title= suggested) (help); Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)
Hanselman, D.H.; T.J. Quinn II; C. Lunsford; J. Heifetz; D.M. Clausen (2003). "Applications in adaptive cluster sampling of Gulf of Alaska rockfish". Fish. Bull. 101 (3): 501–512. {{cite journal}}: Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)
Hobson, E.S.; J.R. Chess; D.F. Howard (2001). "Interannual variation in predation on first-year Sebastes spp. by three northern California predators". Fish. Bull. 99: 292–302.
Kendall, A. W.; W. H. Lenarz (1986). "Status of early life history studies of northeast Pacific rockfishes". Proc. Int. Rockfish Symp. Oct. 1986, Anchorage Alaska. pp. 99–117. {{cite conference}}: Unknown parameter |booktitle= ignored (|book-title= suggested) (help); Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
Kendall, A.W., Jr (2000). "An historical review of Sebastes taxonomy and systematics". Mar. Fish. Rev. 62: 1–16.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Leaman, B. M. (1991). "Reproductive styles and life history variables relative to exploitation and management of Sebastes stocks". Environmental Biology of Fishes. 30 (1–2): 253–271. doi:10.1007/BF02296893.
Leaman, B.M.; R.J. Beamish (1984). "Ecological and management implications of longevity in some Northeast Pacific groundfishes". Int. North Pac. Fish. Comm. Bull. 42: 85–97. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
Li, Z. (2004). "Phylogenetic relationships and identification of juveniles of the genus Sebastes". University of Alaska-Fairbanks, School of Fisheries and Ocean Sciences. M.S. thesis. {{cite journal}}: Cite journal requires |journal= (help)
Longhurst, A. (2002). "Murphy's law revisited: longevity as a factor in recruitment to fish populations". Fish. Res. 56 (2): 125–131. doi:10.1016/S0165-7836(01)00351-4.
Love M.S.; M.M. Yoklavich; L. Thorsteinson (2002). The Rockfishes of the Northeast Pacific. Los Angeles: University of California Press. ISBN 0-520-23437-5. {{cite book}}: Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)
Major, R. L.; H. H. Shippen (1970). "Synopsis of biological data on Pacific ocean perch, Sebastodes alutus". FAO Fisheries Synopsis No. 79, NOAA Circular 347: 38 p. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
PFMC (12 December 2017). "Pacific Ocean Perch Rebuilt". Pacific Fishery Management Council. Retrieved 23 March 2018.
Seeb, L. W.; D.R. Gunderson (1988). "Genetic variation and population structure of Pacific ocean perch (Sebastes alutus)". Can. J. Fish. Aquat. Sci. 45: 78–88. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
Seeb, L. W.; A. W. Kendall Jr (1991). "Allozyme polymorphisms permit the identification of larval and juvenile rockfishes of the genus Sebastes". Environmental Biology of Fishes. 30 (1–2): 191–201. doi:10.1007/BF02296889. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
Withler, R.E.; T.D. Beacham; A.D. Schulze; L.J. Richards; K.M. Miller (2001). "Co-existing populations of Pacific ocean perch, Sebastes alutus, in Queen Charlotte Sound, British Columbia". Mar. Biol. 139 (1): 1–12. doi:10.1007/s002270100560. {{cite journal}}: Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)
Yang, M-S. (1993). "Food habits of the commercially important groundfishes in the Gulf of Alaska in 1990". NOAA Tech. Memo. NMFS-AFSC-22. U.S. Dep. Commer.: 150 p.
Yang, M-S. (1996). "Diets of the important groundfishes in the Aleutian Islands in summer 1991". NOAA Tech. Memo. NMFS-AFSC-60. U.S. Dep. Commer.: 105 p.
Yang, M.S. (2003). "Food habits of the important groundfishes of the Aleutian Islands in 1994 and 1997". AFSC Processed report 2003-07. National Marine Fisheries Service: 233 pp.
Yang, M.-S.; M.W. Nelson (2000). "Food habits of the commercially important groundfishes in the Gulf of Alaska in 1990, 1993, and 1996". NOAA Tech. Memo. NMFS-AFSC-112. U.S. Dep. Commer.: 174 p. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)

Other references

Gulf of Alaska Pacific ocean perch stock assessment (2009)
Bering Sea and Aleutian Islands Pacific ocean perch stock assessment (2008)
Pacific ocean perch NOAA FishWatch. Retrieved 5 November 2012.
Canadian Pacific ocean perch stock assessment (2001)
U.S. West Coast Pacific ocean perch stock assessment (2009)
NOAA's Alaska Fisheries Science Center
"Sebastes alutus". Integrated Taxonomic Information System. Retrieved 1 August 2006.
Froese, Rainer; Pauly, Daniel (eds.). "Sebastes alutus". FishBase. May 2006 version.

v t e Extant Sebastidae species (rockfish)
Adelosebastes	Adelosebastes latens
Helicolenus	Helicolenus alporti Helicolenus avius Bigeye sea perch (H. barathri) Blackbelly rosefish (H. dactylopterus) Helicolenus fedorovi Hilgendorf's saucord (H. hilgendorfii) Helicolenus lahillei Helicolenus lengerichi Helicolenus mouchezi Red gurnard perch (H. percoides)
Hozukius	Hozukius emblemarius Hozukius guyotensis
Sebastes	Rougheye rockfish (S. aleutianus) Pacific ocean perch (S. alutus) Kelp rockfish (S. atrovirens) Brown rockfish (S. auriculatus) Aurora rockfish (S. aurora) Redbanded rockfish (S. babcocki) Sebastes baramenuke Shortraker rockfish (S. borealis) Silvergray rockfish (S. brevispinis) Cape Redfish (S. capensis) Gopher rockfish (S. carnatus) Copper rockfish (S. caurinus) Japanese white seaperch (S. cheni) Greenspotted rockfish (S. chlorostictus) Black-and-yellow rockfish (S. chrysomelas) Dusky rockfish (S. ciliatus) Starry rockfish (S. constellatus) Cortez rockfish (S. cortezi) Darkblotched rockfish (S. crameri) Calico rockfish (S. dallii) Deacon rockfish (S. diaconus) Splitnose rockfish (S. diploproa) Greenstriped rockfish (S. elongatus) Puget Sound rockfish (S. emphaeus) Swordspine rockfish (S. ensifer) Widow rockfish (S. entomelas) Pink rockfish (S. eos) Buccaneer rockfish (S. exsul) Atlantic redfish (S. fasciatus) Sebastes flammeus Yellowtail rockfish (S. flavidus) Bronzespotted rockfish (S. gilli) Gray rockfish (S. glaucus) Chilipepper rockfish (S. goodei) Rosethorn rockfish (S. helvomaculatus) Squarespot rockfish (S. hopkinsi) Sebastes hubbsi Sebastes ijimae Japanese red seaperch (S. inermis) Sebastes iracundus Sebastes itinus Shortbelly rockfish (S. jordani) Sebastes joyneri Sebastes kawaradae Sebastes kiyomatsui Sebastes koreanus Freckled rockfish (S. lentiginosus) Cowcod (S. levis) Sebastes longispinis Mexican rockfish (S. macdonaldi) Atlantic redfish (S. marinus) Quillback rockfish (S. maliger) Red bream (S. matsubarae) Black rockfish (S. melanops) Semaphore rockfish (S. melanosema) Blackspotted rockfish (S. melanostictus) Blackgill rockfish (S. melanostomus) Atlantic redfish (S. mentella) Vermilion rockfish (S. miniatus) Sebastes minor Whitespeckled rockfish (S. moseri) Blue rockfish (S. mystinus) China rockfish (S. nebulosus) Tiger rockfish (S. nigrocinctus) Sebastes nivosus Red perch (S. norvegicus) Sebastes notius Sebastes oblongus Patagonian redfish (S. oculatus) Speckled rockfish (S. ovalis) Sebastes owstoni Sebastes pachycephalus Bocaccio rockfish (S. paucispinis) Sebastes peduncularis Chameleon rockfish (S. phillipsi) Canary rockfish (S. pinniger) Northern rockfish (S. polyspinis) Redstripe rockfish (S. proriger) Grass rockfish (S. rastrelliger) Yellowmouth rockfish (S. reedi) Rosy rockfish (S. rosaceus) Greenblotched rockfish (S. rosenblatti) Yelloweye rockfish (S. ruberrimus) Flag rockfish (S. rubrivinctus) Dwarf-red rockfish (S. rufinanus) Bank rockfish (S. rufus) Stripetail rockfish (S. saxicola) Korean rockfish (S. schlegelii) Sebastes scythropus Halfbanded rockfish (S. semicinctus) Olive rockfish (S. serranoides) Treefish (S. serriceps) Pinkrose rockfish (S. simulator) Blackmouth rockfish (S. sinensis) Sebastes spinorbis Sebastes steindachneri Sebastes swifti Ezo seaperch (S. taczanowskii) Sebastes thompsoni Sebastes trivittatus Honeycomb rockfish (S. umbrosus) Sebastes variabilis Harlequin rockfish (S. variegatus) Sebastes varispinis Japanese black seaperch (S. ventricosus) Norway redfish (S. viviparus) Fox jacopever (S. vulpes) Sebastes wakiyai Pygmy rockfish (S. wilsoni) Sharpchin rockfish (S. zacentrus) Sebastes zonatus
Sebastiscus	Sebastiscus albofasciatus False kelpfish (S. marmoratus) Sebastiscus tertius
Sebastolobus	Shortspine thornyhead (S. alascanus) Longspine thornyhead (S. altivelis) Broadbanded thornyhead (S. macrochir)
Trachyscorpia	Deepsea Scorpionfish (T. carnomagula) Trachyscorpia cristulata Cape rockfish (T. eschmeyeri) Stylish Scorpionfish (T. longipedicula) Trachyscorpia osheri Ecuadorian Deep-sea Scorpionfish (T. verai)