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<br />110 <br /> <br />BESTGEN AND BUNDY <br /> <br />TABLE 4.-Least-squares statistics for regression of lapillus diameter (LD, fLm) as a function of loge (total length, <br />nun) of Colorado squawfish incubated and reared for 165 d with constant temperatures (220C) or with diel temperature <br />fluctuations centered on 18, 22, or 260C, Regressions are LD = a + b.loge (total length). Fish less than 2 d old were <br />excluded from this analysis because their otolith and length measurement residuals were positively biased. <br /> <br /> Intercept: Slope: <br />Treatment df a (SE) b (SE) r2 <br />\8'e fluctuating 45 -\98,\1 (5,47) \06.73 (2,13) 0,983 <br />22'e fluctuating 4\ - 220.20 (6,97) \16,75 (2,60) 0.98\ <br />22'C constant 40 -227,81 (4.62) 120,43 (1.76) 0,992 <br />26'e fluctuating 51 -22237 (5.56) \18,43 (2,14) 0,984 <br />All treatments <br />combined \80 -2]6.72 (3,\2) \15,49 (1.\9) 0,98\ <br /> <br />Somatic Growth versus Otolith Growth <br /> <br />Three experiments were conducted to determine <br />the effects of slow and fast somatic growth rate <br />(experiment 1) and different starvation periods <br />(experiments 2, 3) on otolith growth patterns. <br />When analyzed by ANCOV A, squared values for <br />dependent variables resulted in better fits than loge <br />transformations. Also r2 values for linear equa- <br />tions with squared dependent variables were as <br />high as or higher than those achieved by nonlinear <br />regressions. <br />For experiment 1 (growth rates), ANCOV As in- <br />dicated significant differences in regression slopes <br />between treatments whether dependent variables <br />were squared or log-transformed. This experiment <br /> <br /> 700 <br />........ Slow ~Owlh <br />(\J <br />::s... 600 <br />- Fast~owlh <br />0 <br />UJ <br />'0 500 <br />c: <br />to <br />UJ <br />:3 <br />0 400 <br />..c: <br />~ <br />'- <br />Q) 300 <br />- <br />Q) <br />E <br />to <br />'5 200 <br />UJ <br />~ <br />'is.. 100 <br />to <br />-..J <br /> <br />showed that otoliths of slower-growing fish were <br />larger than otoliths of faster-growing fish of the <br />same length (Figure 1). Fitted equations show, for <br />example, that lapillus diameter of a 25-mm fish <br />was 18% larger in the slow-growth treatment than <br />in the fast-growth treatment. Such an outcome re- <br />sulted from differential treatment effects on so- <br />matic and lapillar growth. A 60-d-old fish in the <br />slow-growth treatment averaged 56% smaller than <br />the same-aged fish in the fast-growth treatment <br />(Figure 2), but its lapilli averaged only 33% small- <br />er (Figure 3). <br />In experiment 2, wherein food was withheld <br />from fish for 6 d between two 6-d feeding periods, <br />somatic growth of starved fish ceased whether <br /> <br /> <br />o <br /> <br />o <br /> <br />10 20 30 40 50 <br />Colorado squawfish TL (mm) <br /> <br />60 <br /> <br />FIGURE l,-Regressions of squared lapillus diameter (LD, /Lm) as a function of Colorado squawfish total length <br />(TL) for fish in slow- and fast-growth treatments, For the slow-growth treatment, LD2 = -135,742.1 + 15,658(TL); <br />r2 = 0,97; N = 40; SE of intercept = 11,293; SE of slope = 485. For the fast-growth treatment, LD2 = -133,328.4 <br />+ 13,984,9(TL); y2 = 0,97; N = 24; SE of intercept = 13,847; SE of slope = 490. <br />