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Biological Opinions - Bureau of Reclamation

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that the proposed action incorporates elements <strong>of</strong> flow variability, real-time disease management,<br />

and restoration activities, which can help to <strong>of</strong>fset some <strong>of</strong> the adverse effects from flow<br />

reductions.<br />

12.4.1.2.4.1 Water Quality<br />

Increases to water temperature in the spring may have both adverse and beneficial effects to coho<br />

salmon juveniles. When water temperatures chronically exceed 16.5 °C, coho salmon juveniles<br />

may become stressed (Sullivan et al. 2000, Campbell et al. 2001 in Ray et al. 2012). However,<br />

increasing water temperature in the spring may also stimulate faster growth (Dunne et al. 2011)<br />

and smolt outmigration (Hoar 1951, Holtby 1988, Moser et al. 1991, Clarke and Hirano 1995),<br />

which may reduce exposure to actinospores and other pathogens in the mainstem Klamath River.<br />

For reasons similar to those discussed for water temperature effects on coho salmon fry (i.e.,<br />

section 12.4.1.2.3.1), when daily maximum water temperatures become chronically above 16.5<br />

°C in May to June, the proposed action will contribute to water temperature conditions that will<br />

be stressful to coho salmon juveniles in the mainstem Klamath River between IGD and the Scott<br />

River (RM 143).<br />

Low dissolved oxygen concentration can impair growth, swimming performance and avoidance<br />

behavior (Bjornn and Reiser 1991). Davis (1975) reported effects <strong>of</strong> dissolved oxygen levels on<br />

salmonids, indicating that at dissolved oxygen concentrations greater than 7.75 mg/L salmonids<br />

functioned without impairment, at 6.0 mg/L onset <strong>of</strong> oxygen-related distress was evident, and at<br />

4.25 mg/L widespread impairment is evident. At 8 mg/L, the maximum sustained swimming<br />

performance <strong>of</strong> coho salmon decreased (Davis et al. 1963, Dahlberg et al. 1968). Low dissolved<br />

oxygen can affect fitness and survival by increasing the likelihood <strong>of</strong> predation and decreasing<br />

feeding activity (Carter 2005). Sublethal effects include increased stress, reduced growth, or no<br />

growth, and are expected for coho salmon parr that are in the mainstem Klamath River below<br />

IGD during the summer and fall.<br />

As discussed in the Effects to Essential Habitat Types section, when the proposed action reduces<br />

mainstem flows in the summer, NMFS expects there will likely be a reduction to dissolved<br />

oxygen concentrations in the mainstem Klamath River between IGD (RM 190) and Orleans (RM<br />

59). Coho salmon juveniles in the mainstem Klamath River between IGD and Orleans will be<br />

exposed to the reduced dissolved oxygen concentrations at night and early morning when they<br />

are not confined to thermal refugia at tributary confluences. Therefore, the proposed actions’<br />

contributions to low dissolved oxygen concentrations in the summer will adversely affect<br />

swimming performance (at ≤ 8.0 mg/L) and increase stress (at ≤ 6.0 mg/L) to coho salmon<br />

juveniles in the mainstem between IGD (RM 190) and Orleans (RM 59) during this period.<br />

12.4.1.2.4.2 Disease<br />

Similar to the discussion on disease effects on coho salmon fry (i.e., section 12.4.1.2.3.3), when<br />

environmental conditions are conducive to actinospore release in the spring (e.g., elevated water<br />

temperature), the proposed action will result in hydrologic conditions in the mainstem Klamath<br />

River that likely support high C. shasta actinospore concentrations (e.g., ≥5 spores/L actinospore<br />

genotype II) that lead to mortality <strong>of</strong> coho salmon juveniles in the mainstem Klamath River<br />

349

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