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t <br />I <br />the appendix (Table 3). Placing the site of a fish location into a par- <br />ticular category was unambiguous in some cases but not in others. The <br />limits of precision in locating radio-tagged fish created some problem <br />t when habitat types were closely juxtaposed such as at shear zones between <br />runs and eddies. Also, the lack of a clear demarcation between some <br />habitat types, such as runs and pools, is a problem inherent in any such <br />categorization. The categorization of a particular site was, therefore, <br />somewhat subjective and relied on the best judgment of the field crew <br />leader. <br />Microhabitat use was characterized by measuring depth, velocity, substrate <br />and temperature at fish locations. Velocity was measured at a depth 60% <br />of the water column (measured from the bottom) at sites < 3.0 ft deep; at <br />sites > 3.0 ft deep, velocity was averaged from two measurements taken at <br />20 and 80% of the water column. In addition to temperature measurements <br />made at the fish location, temperature was also measured at a nearby <br />location in the main channel. In 1987 and 1988, water clarity at a loca- <br />tion (RM 174.4-175.2) in the 15-mile reach was routinely monitored using a <br />standard Secchi disk. <br />Possible spawning sites were identified by the aggregation of ripe adults <br />during the spawning season and, for squawfish, by the subsequent collec- <br />tion of larvae. Post-hatching ages of collected squawfish larvae were <br />calculated using total lengths of individual larvae in age-length equa- <br />tions developed by Haynes and Muth (1985). Spawning date was then esti- <br />mated by subtracting four days from the estimated hatching date. Four <br />days was considered the mean embryo incubation time, based on the 3.8-5.0- <br />7 <br />Ll