Synopsis of Biological Data on the Chum Salmon, Oncorhynchus keta

Synopsis of Biological Data on the Chum Salmon, Oncorhynchus keta Synopsis of Biological Data on the Chum Salmon, Oncorhynchus keta

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Table 39.--Estimated mortality for chum salmon from Hook Nose Creek, British Columbia, during various life stages (Parker, 1962) Life history stage Egg - fry Coastal (juvenile) Pelagic Coastal ( adults) Fishing Total Months 7 5 34 2 48 Survival Percent 7 . 8 5.4 56.6 93 . 0 35.0 0 . 08 Instantaneous mortality (i) 1 2.55 2.91 0 .57 0 . 07 1.05 7 .15 1 Instantaneous mortality (i) loge (N2iNl) where Nl and N2 are the numbers ong>ofong> fish present at times 1 and 2. 4.42 Factors causing or affecting mortality Egg mortality.-- Most ong>ofong> the mortality from egg fertilization to early fry stage occurs while eggs are incubating in the gravel. Hunter (1959), who examined redds in Hook Nose Creek, British Columbia, found that loss ong>ofong> eggs and a levins was 93.6 and 97.9 percent in two y ears. Of there losses 95.9 percent occurred in the pre-eyed stage. In some southeastern Alaska streams, mortalitybefore hatching exceeded 93 percent (McNeil, 1962). Levanidov (1954) found mortality to the alevin stage to be 70 to 75 percent in the Khor River, U.S.S.R. Environmental factors which may influence egg survival ong>ofong> churn salmon are discussed in alphab etical order. Ammonia is a metabolic product ong>ofong> egg respiration which has been suggested (McNeil, 1966) as pos sibly reaching toxic concentrations when the density ong>ofong> eggs and larvae is high and the circulation ong>ofong> intragravel water is poor. Ammonia is the most toxic metabolite ong>ofong> eggs. Carbon dioxide is another metabolic product ong>ofong> eggs. High levels ong>ofong> CO 2 (> 125 mg./ l. milligrams per liter)) in laboratory experiments produced mortality ong>ofong> developing eggs by inhibiting the uptake ong>ofong> oxygen (Alderdice and Wickett, 1958). Oxygen uptake was independent ong>ofong> CO 2 below about 125 mg./ l. The range ong>ofong> free CO 2 in spawning gravel ong>ofong> some southeastern Alaska streams ,vas 2 to 24 mg. 1. (Mc eil, 1962). Intragravel CO 2 in 54 some Russian streams reached 25 to 30 mg./ l. (Levanidov, 1954). CO 2 measured in natural streams has not been shown to influence egg survival. Drought may cause egg mortality directly by leaving redds dry (Smirnov, 1947; Levanidov, 1954; Neave, 1953) or indirectly by allowing other mortality-causing factors to operate. McNeil (1966) and Wickett (1958) found low oxygen and exceptionally high egg mortality when stream discharge was low during and after spawning. Low stream flow led to poor egg survival ong>ofong> the same brood year (1958) in British Columbia, southeastern Alaska, and the Amur River (Ricker and Manzer , 1967; McNeil, 1966; Levanidov, 1964) . In British Columbia, the poor survival was attributed to low discharge and high water temperatures in the fall and in southeastern Alaska and the Amur River, to freezing at low wa ter levels in the winter. Erosion ong>ofong> eggs and young fish from the streambed by floods has long been recognized as a caus e ong>ofong> mortality during incubation (Neave, 1947; Wickett, 1958; Smirnov, 1947). In some southeastern Alaska streams (McNeil, 1966), erosion and shifting gravel destroyed 50 to 90 percent ong>ofong> eggs and larvae in some years. Flooding during the last month ong>ofong> the incubation season in Minter Creek, Wash., reduced fry survival to less than 50 percent ong>ofong> the expected survival (Smoker, 1956). 11 Freezing during periods ong>ofong> low flow can destroy large numbers ong>ofong> incubating eggs. McNeil (1966) concluded that freezing de ­ stroyed up to 65 percent ong>ofong> the eggs in one southeastern Alaskan stream in 1 year. In tributary streams ong>ofong> the Arnur River in the U.S.S.R., freezing in some years resulted in 95-percent mortality (Levanidov, 1954). Smirnov (1947) reported that freezing ong>ofong> ,vater to a depth ong>ofong> 1 m. caused complete egg mortality in other U.S.S.R. streams. Light is detrimental to churn salmon embryos which normally develop in total darkness within the streambed. Direct sunlight is fatal, according to Disler (1953), and indirect sunlight slows the rate ong>ofong> embryo development (Soin, 1954). The harmful effects ong>ofong> light decrease as the embryo grows. Soin (1954) found greater mortality ong>ofong> eggs and lower vitality ong>ofong> fry when eggs were incubated in light than when they were incubated in darkness. 11Smoker, William A. 1956. Preliminary report on Minter Creek biological studies. Part II. Effects ong>ofong> Minter Creek stream flows on the juvenile production ong>ofong> silver salmon, chum salmon, and steelhead trout. Wash. Oep. Fish., 12 pp. text, [8 PP.] figs. (Processed.)

Table 39.--Estimated mortality for chum salm<strong>on</strong><br />

from Hook Nose Creek, British Columbia, during<br />

various life stages (Parker, 1962)<br />

Life history<br />

stage<br />

Egg - fry<br />

Coastal (juvenile)<br />

Pelagic<br />

Coastal ( adults)<br />

Fishing<br />

Total<br />

M<strong>on</strong>ths<br />

7<br />

5<br />

34<br />

2<br />

48<br />

Survival<br />

Percent<br />

7 . 8<br />

5.4<br />

56.6<br />

93 . 0<br />

35.0<br />

0 . 08<br />

Instantaneous<br />

mortality<br />

(i) 1<br />

2.55<br />

2.91<br />

0 .57<br />

0 . 07<br />

1.05<br />

7 .15<br />

1 Instantaneous mortality (i) loge (N2iNl)<br />

where Nl and N2 are <strong>the</strong> numbers <str<strong>on</strong>g>of</str<strong>on</strong>g> fish present<br />

at times 1 and 2.<br />

4.42 Factors causing or affecting<br />

mortality<br />

Egg mortality.-- Most <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong> mortality from<br />

egg fertilizati<strong>on</strong> to early fry stage occurs<br />

while eggs are incubating in <strong>the</strong> gravel. Hunter<br />

(1959), who examined redds in Hook Nose<br />

Creek, British Columbia, found that loss <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

eggs and a levins was 93.6 and 97.9 percent<br />

in two y ears. Of <strong>the</strong>re losses 95.9 percent<br />

occurred in <strong>the</strong> pre-eyed stage. In some<br />

sou<strong>the</strong>astern Alaska streams, mortalitybefore<br />

hatching exceeded 93 percent (McNeil, 1962).<br />

Levanidov (1954) found mortality to <strong>the</strong> alevin<br />

stage to be 70 to 75 percent in <strong>the</strong> Khor River,<br />

U.S.S.R.<br />

Envir<strong>on</strong>mental factors which may influence<br />

egg survival <str<strong>on</strong>g>of</str<strong>on</strong>g> churn salm<strong>on</strong> are discussed in<br />

alphab etical order.<br />

Amm<strong>on</strong>ia is a metabolic product <str<strong>on</strong>g>of</str<strong>on</strong>g> egg<br />

respirati<strong>on</strong> which has been suggested (McNeil,<br />

1966) as pos sibly reaching toxic c<strong>on</strong>centrati<strong>on</strong>s<br />

when <strong>the</strong> density <str<strong>on</strong>g>of</str<strong>on</strong>g> eggs and larvae is high<br />

and <strong>the</strong> circulati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> intragravel water is<br />

poor. Amm<strong>on</strong>ia is <strong>the</strong> most toxic metabolite<br />

<str<strong>on</strong>g>of</str<strong>on</strong>g> eggs.<br />

Carb<strong>on</strong> dioxide is ano<strong>the</strong>r metabolic product<br />

<str<strong>on</strong>g>of</str<strong>on</strong>g> eggs. High levels <str<strong>on</strong>g>of</str<strong>on</strong>g> CO 2 (> 125 mg./ l.<br />

milligrams per liter)) in laboratory experiments<br />

produced mortality <str<strong>on</strong>g>of</str<strong>on</strong>g> developing eggs<br />

by inhibiting <strong>the</strong> uptake <str<strong>on</strong>g>of</str<strong>on</strong>g> oxygen (Alderdice<br />

and Wickett, 1958). Oxygen uptake was independent<br />

<str<strong>on</strong>g>of</str<strong>on</strong>g> CO 2 below about 125 mg./ l.<br />

The range <str<strong>on</strong>g>of</str<strong>on</strong>g> free CO 2 in spawning gravel<br />

<str<strong>on</strong>g>of</str<strong>on</strong>g> some sou<strong>the</strong>astern Alaska streams ,vas 2 to<br />

24 mg. 1. (Mc eil, 1962). Intragravel CO 2 in<br />

54<br />

some Russian streams reached 25 to 30 mg./ l.<br />

(Levanidov, 1954). CO 2 measured in natural<br />

streams has not been shown to influence egg<br />

survival.<br />

Drought may cause egg mortality directly<br />

by leaving redds dry (Smirnov, 1947; Levanidov,<br />

1954; Neave, 1953) or indirectly by<br />

allowing o<strong>the</strong>r mortality-causing factors to<br />

operate. McNeil (1966) and Wickett (1958)<br />

found low oxygen and excepti<strong>on</strong>ally high egg<br />

mortality when stream discharge was low<br />

during and after spawning. Low stream flow<br />

led to poor egg survival <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong> same brood<br />

year (1958) in British Columbia, sou<strong>the</strong>astern<br />

Alaska, and <strong>the</strong> Amur River (Ricker and<br />

Manzer , 1967; McNeil, 1966; Levanidov, 1964) .<br />

In British Columbia, <strong>the</strong> poor survival was<br />

attributed to low discharge and high water<br />

temperatures in <strong>the</strong> fall and in sou<strong>the</strong>astern<br />

Alaska and <strong>the</strong> Amur River, to freezing at low<br />

wa ter levels in <strong>the</strong> winter.<br />

Erosi<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> eggs and young fish from <strong>the</strong><br />

streambed by floods has l<strong>on</strong>g been recognized<br />

as a caus e <str<strong>on</strong>g>of</str<strong>on</strong>g> mortality during incubati<strong>on</strong><br />

(Neave, 1947; Wickett, 1958; Smirnov, 1947).<br />

In some sou<strong>the</strong>astern Alaska streams (McNeil,<br />

1966), erosi<strong>on</strong> and shifting gravel destroyed<br />

50 to 90 percent <str<strong>on</strong>g>of</str<strong>on</strong>g> eggs and larvae in some<br />

years. Flooding during <strong>the</strong> last m<strong>on</strong>th <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong><br />

incubati<strong>on</strong> seas<strong>on</strong> in Minter Creek, Wash.,<br />

reduced fry survival to less than 50 percent<br />

<str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong> expected survival (Smoker, 1956). 11<br />

Freezing during periods <str<strong>on</strong>g>of</str<strong>on</strong>g> low flow can<br />

destroy large numbers <str<strong>on</strong>g>of</str<strong>on</strong>g> incubating eggs.<br />

McNeil (1966) c<strong>on</strong>cluded that freezing de ­<br />

stroyed up to 65 percent <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong> eggs in <strong>on</strong>e<br />

sou<strong>the</strong>astern Alaskan stream in 1 year. In<br />

tributary streams <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>the</strong> Arnur River in <strong>the</strong><br />

U.S.S.R., freezing in some years resulted in<br />

95-percent mortality (Levanidov, 1954). Smirnov<br />

(1947) reported that freezing <str<strong>on</strong>g>of</str<strong>on</strong>g> ,vater to a<br />

depth <str<strong>on</strong>g>of</str<strong>on</strong>g> 1 m. caused complete egg mortality<br />

in o<strong>the</strong>r U.S.S.R. streams.<br />

Light is detrimental to churn salm<strong>on</strong> embryos<br />

which normally develop in total darkness<br />

within <strong>the</strong> streambed. Direct sunlight is<br />

fatal, according to Disler (1953), and indirect<br />

sunlight slows <strong>the</strong> rate <str<strong>on</strong>g>of</str<strong>on</strong>g> embryo development<br />

(Soin, 1954). The harmful effects <str<strong>on</strong>g>of</str<strong>on</strong>g> light<br />

decrease as <strong>the</strong> embryo grows. Soin (1954)<br />

found greater mortality <str<strong>on</strong>g>of</str<strong>on</strong>g> eggs and lower<br />

vitality <str<strong>on</strong>g>of</str<strong>on</strong>g> fry when eggs were incubated in<br />

light than when <strong>the</strong>y were incubated in darkness.<br />

11Smoker, William A. 1956. Preliminary report <strong>on</strong><br />

Minter Creek biological studies. Part II. Effects <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

Minter Creek stream flows <strong>on</strong> <strong>the</strong> juvenile producti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

silver salm<strong>on</strong>, chum salm<strong>on</strong>, and steelhead trout. Wash.<br />

Oep. Fish., 12 pp. text, [8 PP.] figs. (Processed.)

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