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UCREFRP
UCREFRP Catalog Number
7646
Author
Gadomski, D. M. and J. A. Hall-Griswold
Title
Predation by Northern Squawfish on Live and Dead Juvenile Chinook Salmon
USFW Year
1992
USFW - Doc Type
Transactions of the American Fisheries Society
Copyright Material
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<br />r. <br /> <br />, <br /> <br />salmonids from hatcheries, barges, and bypass fa- <br />cilities. <br /> <br />Methods <br /> <br />Fish collection and maintenance.-Northern <br />squawfish (mean fork length, FL, 432.6 mm; SO, <br />36.1; N = 70) were collected from the Columbia <br />River by boat electroshocking and acclimated for <br />at least 3 weeks in indoor 1,400-L circular tanks <br />at temperatures approximating those in the river <br />(l5-170C). They were fed a maintenance diet of <br />live juvenile coho salmon Oncorhynchus kisutch <br />(mean FL, 103.8 mm; SO, 7.2; N = 50) during <br />acclimation and between experiments. The north- <br />ern squawfish were starved for approximately 2 d <br />prior to an experiment. <br />Juvenile chinook salmon O. tshawytscha (mean <br />FL, 90.6 mm; SO, 11.8; N = 100) were used as <br />prey for experiments. Coho and chinook salmon <br />were obtained from the Little White Salmon Na- <br />tional Fish Hatchery complex and held in out- <br />door, 1,400-L circular banks. Tanks received flow- <br />through well water at 6-8"C; juvenile salmonids <br />were not maintained for long periods at higher <br />experimental temperatures because their health <br />deteriorated. Most salmon were acclimated to ex- <br />perimental temperatures for 3 d before a trial be- <br />gan. Due to space constraints, prey were accli- <br />mated to higher temperatures for I h prior to the <br />start of one set of trials (circular tanks with 50% <br />dead prey). Prey to be offered dead were killed by <br />blows to the head shortly before an experiment. <br />Dead fish were given adipose fin clips to distin- <br />guish them from live prey that might die during <br />a trial. <br />Experimental systems. -Experiments were <br />conducted in two indoor fiberglass tank systems. <br />The first system was a series of 1,400-L circular <br />tanks (1.5 m in diameter, 0.8 m deep). A recir- <br />culating-water system supplied each tank with 20 <br />L of filtered well water per minute (Lucchetti and <br />Gray 1988). Temperature was maintained at 15- <br />170C. A natural photoperiod (15 h light: 9 h dark- <br />ness) was simulated; light was provided by a series <br />of fluorescent and incandescent lamps. <br />We also conducted experiments in an 11,300- <br />L, flowing-water raceway (7.6 m long x 1.2 m <br />wide x 1.2 m deep). Temperature was maintained <br />at 16-180C. Five incandescent lights simulated <br />ambient photoperiod (IS h light: 9 h darkness). <br />A centrifugal pump (1,700 Urn in) recirculated <br />water. Because northern squawfish in the field are <br />typically found in areas with flows less than 70 <br />cm/s (Faler et a!. 1988), flow in the raceway was <br /> <br />NOTES <br /> <br />681 <br /> <br />kept at a low velocity. Water velocity varied spa- <br />tially, ranging from about 73 cm/s in midwater <br />upstream to 3 cm/s near the bottom downstream. <br />Proportions of available dead prey. - Three <br />northern squawfish per tank were used for each <br />trial in the circular tanks. Sixty chinook salmon <br />(live plus dead fish) were placed into each tank in <br />the morning; 24 h later, uneaten prey were col- <br />lected and counted. Eighteen trials were conduct- <br />ed with 50% dead juvenile chinook salmon (30 <br />dead and 30 live) and 12 trials with 20% dead <br />chinook salmon (12 dead and 48 live). Prey num- <br />ber was based on maximum daily consumption <br />rates presented by Vigg and Burley (1991). <br />Ten northern squawfish were used for each race- <br />way trial after a minimum IO-d acclimation pe- <br />riod. Trials were conducted during 3-h evening <br />intervals (2000-2300 hours), the first 0.5 h of which <br />was lighted and the remainder of which was in <br />darkness. At the beginning ofa trial, 100 live and <br />dead chinook salmon were placed simultaneously <br />into the raceway at the upstream end. Uneaten <br />prey were removed and counted at the end of 3 <br />h. Three trials were conducted for each percentage <br />of dead prey (50% and 20%). <br />Predation during light and dark periods. - Ex- <br />periments were conducted in circular tanks to de- <br />termine if predation by northern squawfish dif- <br />fered between light (215-270 lux measured 10 cm <br />below the water's surface) and dark (<0.0 I lux) <br />periods. Three northern squawfish per tank were <br />used for each trial. Twenty-two lighted trials were <br />conducted at 0900-1300 hours, and 27 dark trials <br />were conducted at 1800-2200 hours. Three dead <br />(20%) and 12 live juvenile chinook salmon were <br />placed into each tank. Low prey numbers allowed <br />us to visually count live and dead salmon re- <br />maining in a tank without removing them; this <br />was done at 0.5 hand 2 h after the start of II light <br />trials to determine predation rate. <br />Data analysis. - Trials in which more than 50% <br />of the prey were consumed were not included in <br />analyses because if one prey type is selected, the <br />relative abundance ofthe preferred prey decreases <br />as the experiment progresses (Coutant 1973). Each <br />trial was considered a replicate within each of the <br />six experimental conditions (Table I). Ifadequate <br />numbers of prey were consumed per trial, chi- <br />square analysis was used to determine if replicates <br />were homogeneous (Sokal and Rohlf 1981; Zar <br />1984). Ifper-trial consumption was too low for an <br />unbiased chi-square analysis (Zar 1984), trial re- <br />sults for an experimental type were pooled for <br />analysis. Expected ratios of dead and live prey <br />
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