Chum Salmon Oncorhynchus keta
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Chum salmon is an important component of river, estuary and
open ocean ecosystems. Early in life it is eats a variety of
river and estuary insects and becomes prey for predatory fish,
birds and mammals. Later in life, it adds nutrients to the
river ecosystem derived mostly from the Pacific Ocean when its
spawned carcasses decompose and as food for large carnivores
such as
eagles,
bears,
gulls, and
seals (see Quinn 2005 for the role of salmon in river
biodiversity). Chums spawn in small and large streams and
take to the sea soon after hatching. The young salmon disperse
widely and return to the homes stream to spawn 2 to 7 years
later.
For over 40 years, the Mossom Creek hatchery has relied on
volunteers from Centennial School and Port Moody to assist in
caring for eggs and young salmon. A quarter of a million
salmon fry are reared each year at the hatchery. The PWLF
works closely with the Mossom Creek hatchery to assist in
rebuilding coastal ecosystems that enhance the survival of
chum salmon.
Distribution and Migration
The chum salmon has the widest distribution of the salmon
ranging around the north Pacific Ocean (Salo 1991). In British
Columbia, the inner South Coast chums arrive in streams in
summer and fall runs. Summer chums migrate between June and
August, and spawn in September and early October. Fall run
chums migrate from September to November to spawn between
October and January. The migration to the spawning streams by
chum salmon slows as it approaches the destination. Salmon
tagged in Johnstone Strait were recovered in the Strait of
Georgia, the mouth of the Fraser River and in Puget Sound
(Quinn 2005). They travel on average about 25 km/day between
Johnstone Strait and the Fraser River but the journey slows as
they approach the river. In northern Strait of Georgia the
trip slows to about 16 km/day and 10 km/ day in the southern
Strait. The total journey to the Fraser River estuary requires
about three weeks. Another three weeks passes before the
salmon swim upstream, spawn and die.
Population Trend
Salo (1991) reviewed the literature on the life cycle of this
species. In brief, spawning chum salmon are more abundant in
even years and pink salmon are more abundant in odd years in
the Fraser River tributaries (Gallagher 1979). Spawning in
southern British Columbia occurs between early October and
late December (Salo 1991). The young salmon leave the rivers
soon after hatching to grow in estuaries. The food web of the
estuary provides a vital source of food in this process. In
spring, the juvenile chums leave for the ocean in time to
consume plankton blooming in offshore waters. They then move
north to mature in the Gulf of Alaska before returning 3-5
years later to natal streams to spawn and die.
Chum Spawning Behaviour
As the autumn rains fill the creeks and rivers, chums enter
the spawning channels to lay eggs. They swim far upstream
because they prefer the flat early stretches of rivers for
spawning. Males generally precede females to the spawning
beds. Each female
seeks out a stretch of unoccupied gravel to
defend against newcomers. There she digs out a redd with
movements of her tail, testing the depth of the depression
with her anal fin. At the same time, males begin to court
her. A male ready to mate will position himself beside and
slightly behind the female and can be observed crossing back
and forth over her back and sometimes shivering violently.
Large males dominate smaller competitors and get the most
matings but a few small males ( called ‘jacks’) lie in wait
downstream to sneak into position and fertilize eggs at the
same time as the large males are preoccupied in fertilizing
the eggs. Schroder (1982) estimated that these ‘satellite’
males were able to fertilize up to about one quarter of the
eggs. Cutthroat trout ram head on into the side of a ripe
female in order to force eggs out of the vent for consumption.
The female covers her eggs with gravel and begins to build a
second nest. She repeats the same nest building
and egg laying behaviour until three or more nests are
finished. She will remain at the site of these redds
protecting them from overspawning until her energy is depleted
and she drifts downstream to die. Much is known about the role
of stream and water conditions on hatching of chum eggs
(reviewed by Salo 1991) but in general chum eggs hatch between
early March and early May. There is some experimental evidence
that stonefly nymphs scavenge dead chum eggs thus reducing
fungus growth on the living eggs (Nicola 1968).
Upon hatching, alevins wriggle deeper into the gravel and
emerge at night 1-3 weeks later to swim to the estuary. Fraser
River chum migrate between February and June with most
departing between mid-March and the end of April (Beacham and
Starr 1982). The mass migration likely satiates the small
number of predators in small streams allowing most chums a
free passage to the river mouth. Young chum stay up to 3 weeks
in the Fraser and Nanaimo river estuaries, sloughs and nearby
creeks (Healey 1982) and move offshore as the coastal food
supplies dwindle. The prime habitat for chum combines high
carbon input from the river and expansive wetland and
intertidal areas where the carbon is converted into prey eaten
by the salmon. The detritus based food web is the factory that
converts carbon into edible prey for the young chums (Simenstad
et al. 1982). Favoured foods include chironomids (midges),
copepods, adult insects and amphipods (crustaceans) in our
estuaries (Levy and Northcote 1981) that are eaten in large
numbers when high tides provide deepwater access to the
marshes.
The shallow waters of the Strait of Georgia remain their home
until about June.
Then the young chums move into deeper waters and
eventually exit the Strait in July probably in pursuit of
offshore plankton blooms (Salo 1991). There they join immense
schools of sockeye and pink salmon in a broad front along the
coast of British Columbia and Alaska (Hartt 1980). Some late
migrants might not make such a long journey but instead remain
along the outer coast of British Columbia. The schools that
move north into the Gulf of Alaska mature there over the
winter. The time spent at sea allows the salmon to grow
rapidly into a mature fish on a diet of marine invertebrates
and other fish. Most of the growth occurs in June and July and
in the final year before spawning (Ricker 1964). Most chum
salmon mature at 3-5 years of age.
Chum Feeding Behaviour
Juvenile chum salmon enter the Strait of Georgia in southern
Canada in spring when plankton blooms at the mouth of the
Fraser River (Walters et al. 1978). Their entry timing is
likely a balance between food requirements for further growth
and attaining a size where they are willing to risk being
caught by predators. They begin to sample a seafood
smorgasbord of tiny animals known as copepods,
euphasiids, larvaceans, chaetognaths, decapod larvae and
fish larvae and amphipods (Salo 1991). Adult chum eat small
fish such as
herring and
sandlance.
Population Trend
Based on Canadian catch statistics, the number of chums
declined in the early 1940s and spawning returns were likely
low in the early 1920s and 1930s. Catches increased between
1939 and the early 1950s but fell again through the 1960s from
overharvesting (Fisheries and Oceans Canada 2006). By 1985 to
1994, total returns had increased but they dropped again in
the late 1990s. Overfishing and low ocean productivity are
problems for the conservation of chum stocks in recent years
(Beamish et al. 2000). Fall chum salmon migrating through
Johnstone Strait and the Strait of Georgia in the 1990s
encountered seine, gill net and troll fisheries that removed
an average of 68% of the entire Inner South Coast commercial
catch of 800,000 chums annually (Department of Fisheries and
Oceans Canada 2006). The Fraser River fishery harvests
predominately hatchery and rearing channel raised chum salmon
from the Harrison, Chehalis, Inch, Stave and Chilliwack/
Vedder rivers (Fisheries and Oceans Canada 2006).
Ecology of Salmon
One of the
most remarkable ecological stories to emerge in the past few
decades is the vital role of salmon in north Pacific
ecosystems. An excellent review of the story can be found in
Thomas Quinn’s book, The behavior and ecology of Pacific
Salmon and Trout (University of Washington Press, 2005).
Years ago fisheries biologists in Alaska knew that the
carcasses of sockeye salmon enriched otherwise nutrient-poor
lakes where the young sockeye grew before leaving to sea.
Experiments showed that artificial fertilization of lakes
sometimes enhances the growth of young sockeye. It appeared
that the addition of nitrogen and phosphorous increased algal
growth in lakes.
The alga became food of zooplankton eaten by
young sockeye. The next research breakthrough revealed the
role of salmon carcasses in rivers and lakes. With the
development of technology to measure isotopes, scientists were
able to measure the relative contribution of marine and
terrestrial sources of nitrogen and carbon in plants and
animals along riverbanks. Kline et al (1990) showed that
substantial amounts nitrogen and carbon in plants, insects and
fishes was derived from marine sources. Biologists had long
known that bears discard salmon carcasses along the edges of
salmon spawning rivers but it was only recently that the
fuller significance of
bears to the forest ecosystem became clear. The size of
bears and the number of cubs they raise is directly related to
the amount of meat they consume (Hildebrand et al. 1999) and
so large numbers of bears assemble along salmon spawning
streams in autumn. They catch large numbers of large fish but
eat mostly the brains and eggs, discarding about 70% of the
carcass. This remaining protein is left to rot in the forest
where it eventually is taken up by the forest plants, insects,
birds, mammals and fish (Bilby
et al. 1996,
Helfield
2001, Reimchen et al. 2003,
Wilkinson et al 2005).
Chum Salmon Photos
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References
Bilby, R.E., B.R. Fransen and P.A. Bisson. 1996. Incorporation
of nitrogen and carbon from spawning coho salmon into the
trophic
system of small streams: evidence from stable isotopes.
Canadian Journal of Fisheries and Aquatic Sciences 53:164-173.
Bilby, R.E., B.R. Fransen, P.A. Bisson and J.K. Walter. 1998.
Responses of juvenile coho salmon (Oncorhynchus kistusch)
and
steelhead (Oncorhynchus mykiss) to the addition of
salmon carcasses to two streams in southwestern Washington,
U.S.A. Canadian
Journal of Fisheries and Aquatic Sciences 55:1901-1918.
Healey,
M.C. 1991. The life history of chinook salmon. Pp 311-393 in:
Pacific Salmon Life Histories. C. Groot and L. Margolis
(eds).
University of British Columbia
Press.
Helfield,
JM, 2001. Interactions between salmon, bear, and riparian
vegetation in Alaska. PhD thesis, U of Washington, Seattle.
Hilderbrand,
G.V., Schwartz, C.C., Robbins, C.T., Jacoby, M.E., Hanley, T.A.,
Arthur, M.S., and Servheen, C. 1999. The importance
of meat,
particularly salmon, to body size, population productivity,
and conservation of North American brown bears.
Canadian
Journal of Zoology 77: 132–138.
Kline, TC et al. 1993. Recycling of elements transported
upstream by runs of Pacific salmon: 1. Canadian Journal of
Fisheries and
Aquatic Sciences 50-2350-2365.
Quinn, T.P. 2005. The behavior and ecology of Pacific salmon
and trout. UBC Press, Vancouver.
Reimchen,
T. 2003. Some ecological and evolutionary aspects of
bear-salmon interactions in coastal British Columbia. Canadian
Jounral of Zoology 78: 448-458.
Wilkinson, C.E., M.D. Hocking and T.E Reimchen. 2005. Uptake
of salmon-derived nitrogen by mosses and liverworts in coastal
British
Columbia.
Oikos 108: 85-98.
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