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<br />MARKING TECHNIQUES FOR COLORADO SQUA WFISH <br /> <br />909 <br /> <br />.A. <br /> <br />TABLE 2.-Mark-recapture data for autumn 1992 and <br />spring 1993 in a 16-1an reach of the Green River near <br />Jensen, Utah. Abbreviations are j = sample pass, m(j) = <br />number of marked fish captured on pass j, u(j) = number <br />of unmarked fish captured on pass j, M(j) = number of <br />marked fish in the population at beginning of jth sample, <br />N = number of sites sampled (primarily backwaters but <br />occasionally low-velocity side channels), CPUE = catch <br />I1er seine haul. <br /> <br />Dates j m(j) u(j) M(j) N CPUE (SE) <br /> Autumn 1992 <br />22 Sep- 0 383 0 9 NAa <br />13 Oct <br />130ct- 2 5 115 297 18 0.720 <br />14 Oct (0.203) <br />21 Oct- 3 7 150 297 24 1.694 <br />22 Oct (0.717) <br /> Spring 1993 <br />6 Apr- 0 104 0 16 0.483 <br />8 Apr (0.]94) <br />12 Apr- 2 14 74 104 17 0.394 <br />15 Apr (0.122) <br />19 Apr- 3 14 247 183 29 0.828 <br />22 Apr (0.345) <br /> <br />a Only selected backwaters were sampled; thus CPUE was not ap- <br />propriale. <br /> <br />vival averaged 92% (140 of 153 from six back- <br />waters); on five occasions, fish (N = 98) were held <br />overnight and had over 95% survival. <br />Young Colorado squawfish moved only short <br />distances downstream during autumn and spring <br />sampling. In autumn, 10 of 13 (77%) recaptures <br />were from the backwater of origin, as were 25 of <br />27 (93%) fish marked in the spring. Of those fish <br />that moved, all moved less than 3.2 km. We es- <br />timated the probability that a particular fish moved <br />from one 1.6-km stream section downstream to the <br />next section per day was 0.044 for the autumn <br />sampling period. No fish moved from one 1.6-km <br />section downstream to the next section during <br />spring sampling. <br />No marked fish were collected outside the study <br />reach. On 20 October 1992, the first 11.3 km down- <br />I <br />stream of the study reach were sampled and 107 <br />age-O Colorado squawfish were captured; all were <br />unmarked. On 20-21 April 1993, the first 16.2 km <br />downstream of the study reach were sampled and <br />55 yearling Colorado squawfish were captured; all <br />were unmarked. <br />Five Colorado squawfish that were marked in <br />the autumn were caught the following spring. Two <br />were caught in the backwater of origin, two moved <br />downstream (0.3 and 4.2 km), and one moved up- <br />stream (7.4 km). <br /> <br />Parameter Estimates <br />Two biological results influenced our selection <br />of an appropriate model for estimating population <br />size of young Colorado squawfish. Our observa- <br />tion of the limited movement by recaptured fish <br />within and outside the study reach as well as that <br />of Tyus (1991) indicated that the probability of <br />capture changes markedly with temperature and <br />therefore among sampling passes. For these rea- <br />sons we selected model M(t) of Otis et al. (1978) <br />as the best representation of our situation. This <br />model assumed population closure but allowed the <br />probability of capture to vary among sampling <br />passes. <br />We estimated an autumn population size of <br />5,595 (SE, 1,077) with 95% confidence limits of <br />::':::2,112 and a spring population of 2,523 (SE, 490) <br />with 95% confidence limits of ::':::961. Estimates of <br />probability of capture were 0.05, 0.02, and 0.03 <br />for the three sampling passes in the autumn, and <br />0.04,0.03, and 0.10 for the spring. Winter survival <br />was estimated as 0.45 (SE, 0.122) with 95% con- <br />fidence limits of ::':::0.24. <br />Survival estimates were also calculated from <br />CPUE data (Table 2). The first pass during autumn <br />of 1992 consisted of sampling only selected back- <br />waters; thus, CPUE was not calculated for this <br />occasion. Survival was calculated from the re- <br />maining passes; estimates ranged from 0.23 to <br />1.15, and the coefficients of variation (CV = SEt <br />mean) from 0.42 to 0.59 (mean, 0.52). The mean <br />CV was about twice that of the mark-recapture <br />estimate of 0.27. The survival estimate calculated <br />from combined catch per seine haul data (Le., all <br />sampling passes combined), which involved ap- <br />proximately the same seining effort as that for <br />mark-recapture, was 0.49 (SE, 0.210). This was <br />similar to the mark-recapture estimate, but the CV <br />was 1.6 times greater. <br /> <br />Simulations <br />Under the study sampling regime (16-km reach, <br />three sampling passes, probability of capture rang- <br />ing from 0.02 to 0.05 in the autumn and from 0.03 <br />to 0.10 in the spring), simulated CVs were 0.23 <br />and 0.18 for autumn and spring population esti- <br />mates, respectively (trials 1, 2; Table 3). As ex- <br />pected, these values were similar to the empirical <br />values (CV = 0.19 for both autumn and spring). <br />The relative biases due to small samples were 5.7% <br />and 3.2%, and at the most likely rate of immigra- <br />tion-emigration (probability a fish moves down- <br />stream from a 1.6-km reach to the next is 0.044 <br />per day), relative bias increased to 14.5% (trial 9). <br />