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Electrical Power for Valdez and the Copper River Basin-1981

Electrical Power for Valdez and the Copper River Basin-1981

Electrical Power for Valdez and the Copper River Basin-1981

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emergence <strong>and</strong> outmigration of fry to Port <strong>Valdez</strong> at a time when itis questionable that <strong>the</strong>re would be adequate planktonic productionto sustain rearing activity. Consequently, a substantial alterationin natural water temperature during <strong>the</strong> egg to fry developmentperiod would negatively impact run strength.With sufficient data, <strong>the</strong> number of temperature units required <strong>for</strong>eggs to hatch under natural stream temperatures can be calculated<strong>and</strong> compared to <strong>the</strong> number of temperature units anticipated to existunder altered stream conditions. The difference in temperatureunits will show if early or late emergence will occur, <strong>and</strong> if so,give <strong>the</strong> approximate magnitude of change in <strong>the</strong> time of emergence.Where intertidal spawning occurs, such as in Allison Creek, <strong>the</strong>warmer saltwater contributes to higher intragravel temperatures.This adds to <strong>the</strong> complexity of <strong>the</strong> temperature regime in intertidalareas because intertidal zone temperatures are influenced by (1)upstream water temperatures, (2) saltwater temperatures exposed tostream gravel, (3) time of exposure to saltwater, <strong>and</strong> possibly (4)<strong>the</strong> permeability of gravels.Should early fry emergence occur, sufficient food sources may notexist. Figure 4 illustrates <strong>the</strong> seasonal variation in populationdensity of <strong>the</strong> copepod, Harpacticus uniremis, an organism whichcould be an important food source <strong>for</strong> post-emergent fry. Healey(1979) found that H. uniremis made up 50% of <strong>the</strong> overall diet ofjuvenile chum salm~n in <strong>the</strong> Nanaimo Estuary <strong>and</strong> greater than 80%of <strong>the</strong> diet when fry were most abundant. He also found that<strong>the</strong> seasonal pattern of abundance of fry <strong>and</strong> H. uniremis in <strong>the</strong>estuary was <strong>the</strong> same, <strong>and</strong> that fry consumed most of <strong>the</strong> estimatedproduction of H. uniremis. Large numbers of this copepod are usuallynot present in Port <strong>Valdez</strong> until mid-March to early April. Undernatural conditions pink <strong>and</strong> chum salmon fry emergence begins inmid-April in <strong>the</strong> Port <strong>Valdez</strong> area.Radical fluctuations in stream flow contribute most heavily tomortality of developing eggs through erosion, shifting of gravel, ordewatering of spawning beds. Flooding also causes mortality bydeposition of silt on spawning areas, which slows intragravel watermovement, decreasing <strong>the</strong> oxygen supply to <strong>the</strong> eggs, <strong>and</strong> preventingremoval of waste products. O<strong>the</strong>r factors contributing to mortalityof eggs are freezing, exposure to light, parasites, predation, highsalinity, shock, <strong>and</strong> superimposition of redds (spawning beds).The tailrace discharge could cause increased velocity in <strong>the</strong> stream<strong>and</strong> scouring of <strong>the</strong> streambed with subsequent removal or burial ofspawning gravel. Alterations in natural streamflow could also haveadverse impacts upon spawning adults as a result of ei<strong>the</strong>r high orlow flows which are not optimum <strong>for</strong> spawning. Post-project flowschedules could be beneficial to fish resources by reducing radicalflow fluctuations <strong>and</strong> providing flows optimum <strong>for</strong> life stage requirementsof pink <strong>and</strong> chum salmon.

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