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Last modified
7/14/2009 5:02:28 PM
Creation date
5/22/2009 4:44:29 PM
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UCREFRP
UCREFRP Catalog Number
7019
Author
Hawkins, J. A.
Title
Age and Growth Of Colorado Squawfish From the Upper Colorado River Basin, 1978-1990.
USFW Year
1991.
USFW - Doc Type
Fort Collins, CO.
Copyright Material
NO
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<br />4 <br /> <br />sides of equation (I) giving: <br /> <br />log10 W = IOg10 0 + b IOg10 L, <br /> <br />(2) <br /> <br />where 10glo 0 is the intercept and b is the slope of the line. These constants are estimated by <br />either least-squares (ordinary major axis) or geometric-mean (standard major axis) regression. <br />The geometric-mean method is often recommended because weight is not truly independent of <br />length and both are subject to errors or fluctuations (Ricker 1973, 1975a and 1975b; Anderson <br />and Gutreuter 1983; Bolger and Connolly 1989), but this method has been considered <br />inappropriate and difficult to interpret (Sprent and Dolby 1980; Cone 1989). Least-squares <br />regression is commonly used due to its "better understood" statistical properties (Bolger 'and <br />Connolly 1989; Jolicoeur 1975). An excellent review of methods for determining the <br />weight-length relationship was provided by Le Cren (1951). <br /> <br />: , <br /> <br />Fish from each of the four major rivers (Colorado, Green, White, and Yampa) were <br />grouped by month of capture, and a regression was calculated by the least-squares method using <br />equation (2). An analysis of co-variance between months was performed on regression equations <br />using SAS statistical packages (SAS Institute. Cary, N.C.) for micro-computer. <br /> <br />The regression equation of weight and length provides a good description of a population <br />or subgroup, but a comparison between groups is not easy because two parameters (0 and b) must <br />be considered (Bolger and Connolly 1989). Often only slopes are compared, with larger slopes <br />indicating faster growth and therefore better condition, but slopes should be compared only when <br />intercepts are equal (Bolger and Connolly 1989). If slopes of different subgroups are equal, as <br />determined by analysis of covariance, then intercepts are good indicators of the condition of each <br />group (Le Cren 1951; Bolger and Connolly 1989). . <br /> <br />Condition indices <br /> <br />Condition factor is derived by rearranging equation (1) into: <br /> <br />0- W. . <br />-[}i <br /> <br />(3) <br /> <br />A condition factor often used is Fulton's condition factor (K): <br /> <br />K = Jf.,-. * 10 n <br />L.;J , <br /> <br />(4) <br /> <br />where n equals 2, 3, 4, or 5 depending on units of measure. The scaling constant (n) converts the <br />result to a mixed number for better comprehension (Anderson and Gutreuter 1983; Cone 1989). <br />K represents growth of an idealized fish with isometric growth where weight is proportional to <br />length cubed. K is easy to calculate and does not require knowledge of the weight-length <br />relationship, but problems with K are many. K will vary for the same fish depending on whether <br />metric or English measurements are used (Anderson and Gutreuter 1983). It assumes that growth <br />is isometric (b=3). Fish of different sizes cannot be compared because K will increase with length <br />if b for the population is greater than 3. Anderson and Gutreuter (1983) suggested limiting <br />comparisons to similar lengths. Cone (1989) cautioned that each stratum (e.g. sex, strain, growth <br />stanza) to be compared should be cheCked to confirm isometric growth. <br /> <br />Although used regularly, Fulton's condition was determined inappropriate because it does <br />not account for allometric growth. Instead, relative condition (Kn) was calculated for individual <br />fish from each river with the formula: <br /> <br />Kn = W b* 100 <br />oL ' <br /> <br />(5) <br />
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