Oncorhynchus tshawytscha (Walbaum in Artedi, 1792)

Common Name: Chinook Salmon

Synonyms and Other Names:

king salmon



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Identification: Chinook salmon is characterized by small dark spots on the head, back, and caudal fin, black gums on the lower haw, and a fusiform, streamlined, and laterally compressed body. Sea run fish are dark green to blue-black on their heads and back and silvery to white on the sides and belly. Chinook salmon changes to an olive-brown, red, or purplish color during spawning. See also Moyle (1976a); Scott and Crossman (1973); Wydoski and Whitney (1979); Morrow (1980); Eschmeyer et al. (1983); Page and Burr (1991).


Size: up to 147 cm


Native Range: Arctic and Pacific drainages from Point Hope, Alaska, to Ventura River, California. Occasionally strays south to San Diego, California. Also in northeastern Asia (Page and Burr 1991).


Great Lakes Nonindigenous Occurrences: Chinooks have been stocked in the Colorado basin in Colorado (Wiltzius 1985; Horak, personal communication); unspecified areas in Connecticut (Whitworth 1996); the Delaware and Nanticoke rivers in Delaware (Raasch and Altemus 1991); Kaui, Hawaii (Brock 1960; Maciolek 1984) islands of Kauai and Hawaii (Mundy 2005); the Spokane drainage in Idaho (Idaho Fish and Game 1990, 1996, 1997); Lake Michigan, Illinois (Parsons 1973; Smith 1979; Emery 1985; Underhill 1986; Burr 1991); Lake Michigan and Indiana Dunes National Lakeshore, Indiana (Nelson and Gerking 1968; Parsons 1973; Emery 1985; Underhill 1986; Tilmant 1999); the Missouri River, Iowa (Baird 1876 in Jones 1963); unspecified areas in Kansas (Cross 1967); Tangipahoa and Notalbany rivers, Louisiana (Bean 1882); Swan, Damariscotta, Cobboseecontee, and Long lakes and Pemaquid River, Maine (Kendall 1914a; Everhart 1950); lower Susquehanna, upper Chesapeake, Gunpowder, Patapsco, Patuxent, Potomac, Monocacy, and Conococheague drainages in Maryland (Ferguson 1876); the Shawsheen, Saugus, North, Ipswich, Merrimack, and Nashua rivers, Lake Quinsigamond in Worcester County, and an unnamed river in Bridgewater, Plymouth County, Massachusetts, in historic times and in the North River in recent times (1989) (Hartel 1992; Cardoza et al. 1993); the Great Lakes surrounding Michigan and Isle Royale National Park and the Sleeping Bear Dunes National Lakeshore (Parsons 1973; Phillips et al. 1982; Emery 1985; Underhill 1986; Michigan Department of Natural Resources 1997; Tilmant 1999; Cudmore-Vokey and Crossman 2000); Lake Superior, and numerous inland lakes in Minnesota (Parsons 1973; Eddy and Underhill 1974; Phillips et al. 1982; Emery 1985; Underhill 1986); Fort Peck Reservoir and the Missouri River, Montana (Holton 1990; Young et al. 1997); the Missouri, Big Blue, Platte, North Platte, Loup, and Elkhorn rivers, Salt Creek, and Birdwood Creek, Nebraska (Jones 1963; Morris et al. 1974) and Lewis and Clark Lake (Nebraska Game and Parks Commission); lakes and rivers in the central Lahontan basin, Nevada (Smith 1896; Miller and Alcorn 1946; La Rivers 1962); two unspecified rivers and large oligotrophic lakes in New Hampshire, including Sunapee, First Connecticut, Squam and Ossippee lakes, Round Pond in Pittsburg (Hoover 1936; Bailey and Oliver 1939; McAffee 1966; Cooper 1983; Schmidt 1986); the Raritan and Delaware rivers in New Jersey (Nelson 1890; Fowler 1906, 1952; Raasch and Altemus 1991); Lake Ontario, Lake Erie, Little Moose Lake in Herkimer County (CU 73659), and Green Lake State Park in Onondaga County (CU 72033), New York (Parsons 1973; Smith 1985; Vinyard 2001; Craine 2002); the Missouri River (Lake Sakakawea) in North Dakota (Cross et al. 1986; North Dakota Game and Fish Department 1994, 1997); Lake Erie and its tributaries, and the Tuscarwas, Muskingum, Scioto, and Great Miami drainages in Ohio (Trautman 1957; Parsons 1973; Trautman 1981; Underhill 1986); the Delaware and Susquehanna rivers, and Lake Erie, Pennsylvania (Bean 1892b; Parsons 1973; Cooper 1983; Underhill 1986); Lake Oahe and other unspecified locations in South Dakota (Cross et al. 1986; Marrone 1996; North Dakota Game and Fish Department 1994; Hanten, personal communication); unspecified locations in Texas (Howells 1992a); Fish Lake, Utah (Sigler and Miller 1963; Sigler and Sigler 1996); the Potomac, James, Dan, New, and North and South Fork Holston rivers, Virginia (Ferguson 1876; Jenkins and Burkhead 1994); unspecified locations in Vermont (Cox, personal communication); the Potomac drainage in West Virginia (Cincotta, personal communication); Riley Lake in Chippewa County, Stormy and Pallette lakes in Vilas County, Lakes Michigan and Superior, and Apostle Islands National Lakeshore, Wisconsin (Parsons 1973; Phillips et al. 1982; Becker 1983; Emery 1985; Underhill 1986; Tilmant 1999).


Table 1. Great Lakes region nonindigenous occurrences, the earliest and latest observations in each state/province, and the tally and names of HUCs with observations†. Names and dates are hyperlinked to their relevant specimen records. The list of references for all nonindigenous occurrences of Oncorhynchus tshawytscha are found here.

Full list of USGS occurrences

State/ProvinceFirst ObservedLast ObservedTotal HUCs with observations†HUCs with observations†
18732000*
IL196720212Lake Michigan; Little Calumet-Galien
IN196820123Lake Michigan; Little Calumet-Galien; St. Joseph
MI1870201324Au Gres-Rifle; Betsie-Platte; Betsy-Chocolay; Black-Presque Isle; Boardman-Charlevoix; Fishdam-Sturgeon; Huron; Kalamazoo; Lake Erie; Lake Huron; Lake Michigan; Lake St. Clair; Lake Superior; Lone Lake-Ocqueoc; Lower Grand; Manistee; Muskegon; Ontonagon; Pere Marquette-White; Pigeon-Wiscoggin; Shiawassee; St. Clair; St. Joseph; Upper Grand
MN187820063Baptism-Brule; Beaver-Lester; Lake Superior
NY187320167Black; Irondequoit-Ninemile; Lake Erie; Lake Ontario; Oneida; Raisin River-St. Lawrence River; Salmon-Sandy
OH187720035Cedar-Portage; Huron-Vermilion; Lake Erie; Lower Maumee; Sandusky
PA198319831Lake Erie
WI1876201415Beartrap-Nemadji; Door-Kewaunee; Duck-Pensaukee; Great Lakes Region; Lake Michigan; Lake Superior; Lower Fox; Manitowoc-Sheboygan; Menominee; Milwaukee; Oconto; Peshtigo; Pike-Root; St. Louis; Upper Fox

Table last updated 4/19/2024

† Populations may not be currently present.

* HUCs are not listed for areas where the observation(s) cannot be approximated to a HUC (e.g. state centroids or Canadian provinces).


Ecology: Chinook salmon are anadromous, migrating from streams to the ocean to grow and mature and returning to their natal streams to spawn. Fry may migrate to sea after as few as three months or as many as three years, but most stay one year instream. Instream, chinook feeds mainly on macroinvertebrates; after migrating from the stream, it feeds primarily on small forage fish. Landlocked Chinook salmon in the Great Lakes usually leaves its natal stream for the lake proper within a few months of hatching (Michigan DNR 2011).


Means of Introduction: Authorized introductions for sportfishing. Stocking began as early as 1874 in several states. Parsons (1973) give detailed accounts of stockings in the Great Lakes. The first stocking of large numbers of Chinook salmon in the Great Lakes occurred in 1967 in Lake Michigan and Lake Superior in part to control alewfie. Chinook salmon was first planted into Lake Superior in 1967 by the state of Michigan. This introduction was extended to Minnesota in 1974, Wisconsin in 1977, and Ontario in 1988. Annual plants of spring fingerlings between 1989 and 1991 averaged approximately 350,000 in Michigan, 509,000 in Minnesota, 384,000 in Wisconsin, and 300,000 in Ontario. By 1970 the species had been planted in all the Great Lakes (Parsons 1973). Between 1873 and 1933, about 11 million Chinook salmon were stocked in the Great Lakes basin (Parsons 1973). In a second attempt to establish chinook, another six million were stocked 1967-1970. Stocking numbers of Chinook salmon in Lake Ontario peaked in 1984 at 4.2 million fish and ranged from 3.2 million to 3.6 million annually from 1984 to 1992. From 1994-1996, stocking ranged from 1.5-1.7 million fish and from 1997-1999 stocking ranged from 2.0-2.2 million fish (Mills 2003). From the mid-1980s to 1992, the Michigan DNR stocked approximately 3.5 million Chinook salmon fingerlings into Lake Huron (Ebner 1995). Chinook salmon was stocked in West Virginia in 1874 (Cincotta, personal communication). Chinook salmon was also stocked in Nevada, but became extinct by 1911 (Vinyard 2001). Chinook salmon was stocked into Lake Sakakawea, North Dakota since 1976 using eggs collected from Lake Michigan fish. Beginning in 1982 it was also stocked downstream into Lake Oahe, South Dakota (Marrone 1996).


Status: Chinook salmon have been found to spawn and reproduce in the Great Lakes (Negus 1995; Peck 1999). In Lake Huron, 7 out of every 8 chinook salmon in the population come from natural reproduction (Michigan DNRE 2011). Chinook salmon is the most heavily stocked species in Lake Ontario (Kerr 1991). Chinook salmon is no longer present in Utah (Sigler and Sigler 1996).


Great Lakes Impacts:
Summary of species impacts derived from literature review. Click on an icon to find out more...

EnvironmentalBeneficial


 

Oncorhynchus tshawytscha has a high environmental impact in the Great Lakes.

Realized:
In the Great Lakes, chinook salmon competes with native lake trout (Salvelinus namaycush) (Page and Laird 1993). Scott et al. (2003) found that the presence of chinook salmon causes delayed nesting and reduced survival of Atlantic salmon (Salmo salar) during spawning in Lake Ontario. Additionally, Atlantic salmon was generally more active and males engaged in more agonistic behavior (head-down, lateral display, parallel swim) when chinook salmon was present. Such effects could have a negative impact on present Atlantic salmon restoration efforts.

The introduction of Pacific salmonines is deemed responsible for the introduction of Renibacterium salmoninarum, which causes bacterial kidney disease in lake trout, brook trout (S. fontinalis), lake whitefish (Coregonus clupeaformis), and bloater (C. hoyi). However, the specific role of chinook salmon in this introduction is unknown (see GLANSIS fact sheet for R. salmoninarum).

Crawford et al. (2001) pointed out that salmonids have the potential to alter the energy and nutrient cycles of the Great Lakes system through increased energy transfer between open water and streams/tributaries. This energy transfer includes the addition of nitrogen and phosphorus to tributaries through decaying salmonine carcasses, as well as the addition of salmon eggs and dead fish as a food source in streams (Ivan et al. 2011, Parmenter and Lamarra 1991, Rand et al. 1992). Rand et al. (1992) found that phosphorus released from salmon carcasses was responsible for >50% of the total phosphorus discharged in some Lake Ontario streams during parts of the spring. The presence of live salmonids may have an even greater effect on nutrients in streams through the excretion of ammonium and soluable reactive phosphorus and their mechanical disturbance of the stream bottom during spawning runs (Ivan et al. 2011, Tiegs et al. 2009).

Potential:
Chinook salmon is a predatory fish and may impact populations of smaller fishes. Some agencies in lakes Michigan and Ontario drastically reduced their stocking quotas for chinook salmon in the 1990s and are concerned about their impact on the fish community, namely declining populations of alewife (Alosa pseudoharengus) and other forage fish (Schreiner 1995). Jones (1993) predicted that maintaining high levels of predator demand by stocking Chinook salmon and other top predators at the current rate would eventually lead to an alewife collapse, possibly followed by the further collapse of other small forage fish populations. Chinook salmon had totally eliminated rainbow smelt (Osmerus mordax) in two small New Hampshire lakes where the salmon was stocked to control the smelt (McAffee 1966).

Negus (1995) proposed that stocking of Chinook salmon in Lake Superior could be modified to alter predation pressure on important prey species. However, hatchery-reared Chinook salmon was found to make up only 25% of the sport fish catch in Lake Superior—such lack of predominance indicating that Chinook salmon have become naturalized and stocking efforts may only marginally affect Chinook salmon biomass in the lake (Peck 1999). Hatchery-reared Chinook salmon in Lake Huron only contributes 1 out of every 8 fish in the population (MIDNRE 2011).

There is little evidence to support that Oncorhynchus tshawytscha has significant socio-economic impacts in the Great Lakes.

As this species is intentionally stocked for recreation, there are no negative impacts on human health or recreation associated with this species.

Oncorhynchus tshawytscha has a high beneficial effect in the Great Lakes.

Realized:
Since the introduction of chinook salmon to control alewife populations in the 1960s, chinook salmon has remained an important component of the Great Lakes fisheries and is recreationally and economically valuable. It was estimated that of the five most-stocked non-native salmonine species (O.kisutch, O. kisutch, O. mykiss, O. tshawytscha, S. trutta, S. salar), chinook salmon constituted 45% of all stockings before 1998 (Crawford 2001). It is most commonly fished in open water, but is also fished as a fall stream species (especially off of Lake Ontario) (Bence and Smith 1999). From 1967 to 1993, over 259 million chinook salmon were stocked in the Great Lakes (Kocik and Jones 1999). In 2005, nearly 9.5 million chinook salmon were stocked in the Great Lakes system (not including Lake Erie) as reported by various agencies (USFWS/GLFC 2010). Most were stocked in Lake Michigan (4,000,000+) followed by Lake Huron (2,500,000+) (USFWS/GLFC 2010). A 2005 survey of anglers fishing in Canada reported an annual recreational harvest of 426,890 chinook salmon in the Great Lakes system (Fisheries and Oceans Canada 2008). Additionally, chinook salmon is a significant catch of the Native American commercial harvest, especially in Lake Huron (Bence and Smith 1999).

Potential:
Eggs spawned by chinook salmon have been found to comprise an important part of the native brown trout diet in Great Lakes tributaries, but the effects of this consumption have yet to be understood (Ivan et al. 2011).


Management: Pacific salmon were first introduced to the Great Lakes in the 1960s to manage alewife populations. Soon after, the multi-million dollar Great Lakes Pacific salmon sportfishery was established and is now one of the largest economic sectors in the region. Therefore, Pacific salmon management objectives are not geared towards the removal or eradication of the species like with most invaders, but rather to maintain or enhance the health and stability of the fisheries. Managers and citizens understand that with over 180 nonindigenous species, the Great Lakes are not the same ecosystem they once were. Management efforts still focus on the prevention and eradication of harmful invaders, but also realize that non-native Pacific salmon fisheries are one of the driving economic forces in the Great Lakes and managers need to account for this. Pacific salmon management is extremely diverse, integrated, and cascading and is therefore these are the most heavily regulated species (direct and indirectly) in the Great Lakes.

Regulations (pertaining to the Great Lakes region)
Direct Regulations:
Great Lakes states and provinces have their own specific fishing regulations. Generally, the overall goals and objectives of Pacific salmon fishing regulations are the same throughout the region i.e., to maintain or enhance a healthy and sustainable salmonid fisheries. Pacific salmon fishing regulations include daily and season bag limits, size limits, permitted baitfish, manner of taking i.e., snagging or hook and line, and designated season dates (See New York DEC, Pennsylvania F&BC, Ohio DNR, Michigan DNR, Indiana DNR, Illinois DNR, Minnesota DNR, Wisconsin DNR, Ontario MNR, and Quebec MRNF websites for specific fishing regulations). 

Indirect Regulations:
Typically, Pacific salmon regulations are not species specific, but rather regulate the salmonid fisheries as a whole. Indirect Pacific salmon regulations include mandated salmonid pathogen screening tests and baitfish regulations.
Mandatory salmonid pathogen screening tests are implemented in all Great Lakes states and provinces. The importation, exportation, and transportation of Pacific salmon is highly regulated to control the spread of infectious diseases and parasites such as VHS, BKD, and whirling disease (See USGS nonindigenous diseases and parasites fact sheets for state and provincial regulations).
State and provincial baitfish regulations have aided in preventing the spread of infectious disease. Specific and or stricter regulations are placed on baitfish species that are known carriers of salmonid pathogens.

Note: Check federal, state/provincial, and local regulations for the most up-to-date information.
Control
Biological
Pacific salmon prey heavily upon two non-native species in the Great Lakes, the alewife (Alosa pseudoharengus) and rainbow smelt (Osmerus mordax).   Alewives remain a key food source and crucial to the survival of Pacific salmon.  Over the past several decades, Pacific salmon populations have fluctuated with fluctuating alewife populations. Managing one species significantly impacts the other. Pacific salmon and alewives have significant environmental, socio-economic, and beneficial effects in the Great Lakes and therefore integrated management is essential. Rainbow smelt are also a major component of Pacific salmon diet. Similar to alewives, Pacific salmon and rainbow smelt management should be integrated.  Rainbow smelt have a high environmental impact and high beneficial effect in the Great Lakes. The presence or absence of this species significantly alters predator-prey relationships and competition between native species. Managers can also attempt to increase less harmful native prey species stocks while allowing harmful invasive prey species to decrease.  Implementation of this bio-control has potential significant beneficial effects in the Great Lakes with few negative impacts (See USGS fact sheets on alewife and rainbow smelt).

Of the 23 nonindigenous diseases and parasites in the Great Lakes, Aeromonas salmonicida, Renibacterium salmoninarum, Myxobolus cerebralis, and Novirhabdovirus sp. infections have been realized in Great Lakes Pacific salmon, while Heterosporosis sp. and Piscirickettsia cf. salmonis infections have been realized clinically or outside the Great Lakes. Glugea hertwigi, a microsporidian, is known to cause mortality in rainbow smelt. Therefore, Pacific salmon management must include the management of the above pathogens and parasites (See USGS fact sheets on Aeromonas salmonicida, Renibacterium salmoninarum, Myxobolus cerebralis, Novirhabdovirus sp., Heterosporosis sp., Piscirickettsia cf. salmonis, and Glugea hertwigi for information on Great Lakes impacts and management).

Physical
Aquaculture facilities manage wild and cultured Pacific salmon stocks through wild stock assessments and other methods. Managers are then able to make informed decisions on stocking strategies. Research, pathogen screening, and pathogen treatment, etc. is conducted in aquaculture facilities (See state and provincial DEC, MNR, DNR, and corresponding agency and department websites for information on salmonid aquaculture and state hatcheries).

Chemical
Chemical controls for Pacific salmon are not intended to eradicate or kill the species but rather to protect it against infectious disease. Typically, depending on the target species, chemicals controls are only effective in aquaculture or similar systems. Examples of chemicals used and include Furogen®, chlorination, and disinfectants.

Note: Check state/provincial and local regulations for the most up-to-date information regarding permits for control methods. Follow all label instructions.


Remarks: Chinook salmon has not been stocked in Oklahoma (Pigg, personal communication). Parsons (1973) gave detailed stocking information for the Great Lakes. During the 1970s, nearly all Chinook salmon in the Great Lakes reached sexual maturity by age 3. in the 1990s, however, 20% became sexually mature at age 4 (Ebner 1995). Lakewide average weight (kg) at age in Lake Huron is 1.8 kg at age 1, 5.2 kg at age 2, 7.2 kg at age 3, and 8.1 kg at age 4. (Ebner 1995). Wurster (2005) found that Chinook salmon in Lake Ontario occupy epilimnetic waters approaching their upper lethal limit of 22°C in the summer months, presumably because the highest prey fish biomass is found near 20°C. Rand (1998) estimated survival rates of stocked Chinook salmon in Lake Ontario to be 45% to 47%.


References (click for full reference list)


Author: Fuller, P., G. Jacobs, M. Cannister, J. Larson, and A. Fusaro


Contributing Agencies:
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Revision Date: 12/20/2019


Peer Review Date: 6/26/2014


Citation for this information:
Fuller, P., G. Jacobs, M. Cannister, J. Larson, and A. Fusaro, 2024, Oncorhynchus tshawytscha (Walbaum in Artedi, 1792): U.S. Geological Survey, Nonindigenous Aquatic Species Database, Gainesville, FL, and NOAA Great Lakes Aquatic Nonindigenous Species Information System, Ann Arbor, MI, https://nas.er.usgs.gov/queries/greatlakes/FactSheet.aspx?Species_ID=920&Potential=N&Type=0&HUCNumber=DHuron, Revision Date: 12/20/2019, Peer Review Date: 6/26/2014, Access Date: 4/19/2024

This information is preliminary or provisional and is subject to revision. It is being provided to meet the need for timely best science. The information has not received final approval by the U.S. Geological Survey (USGS) and is provided on the condition that neither the USGS nor the U.S. Government shall be held liable for any damages resulting from the authorized or unauthorized use of the information.