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<br />404 <br /> <br />COPEIA, 2000, NO.2 <br /> <br />water temperatures below unmodified hypolim- <br />nial-release dams in the basin are near 10 C <br />year-round, whereas spring-summer tempera- <br />tures in river reaches unaffected by dams ap- <br />proach 20 C (U.S. Geological Survey records). <br />Our 14 C experimental temperature simulated <br />mixing of tributary and mainstem tailwater <br />flows or eddy return channels and other low- <br />velocity "backwater" habitats in tailwater reach- <br />es that may warm above main channel temper- <br />atures. <br />Because early life stage fishes may drift (Ber- <br />ry, 1988; Robinson et aI., 1998), be transported <br />via flood (R. Valdez and Ryel, R. J. unpubI.), or <br />actively disperse from spawning streams into <br />tailwater reaches, we examined temperature ef- <br />fects on three age groups (7 days, 14 days, and <br />41 days posthatch) of each species to evaluate <br />effects of differential timing of entrance to cold <br />tailwaters from warm tributaries. <br />Eighteen 38-liter aquaria were individually <br />supplied with recirculating hatchery water in- <br />side the temperature-controlled lab under nat- <br />ural light conditions supplemented with illumi- <br />nation from wide spectrum fluorescent lights <br />during daytime. Two one-quarter-hp chillers <br />equipped with mechanical, biological, and <br />chemical filters were connected to two sets of <br />six aquaria maintained at 10 ::!:: 0.5 C and 14 ::!:: <br />0.5 C, respectively. A third set of six aquaria was <br />supplied with ambient 20 ::!:: 0.5 C water but was <br />otherwise treated identically. Temperatures in <br />each aquarium were monitored daily with maxi <br />min thermometers. <br />Growth experiments were initiated with 6-8- <br />day (hence age 7-day) , 13-15-day (hence age 14- <br />day), and 39-43-day (hence age 41-day) post- <br />hatch groups of each species. Swim-up (7-day) <br />larvae were acclimated to 20 C for a minimum <br />of 24 h prior to initiation of experiments, <br />whereas older age groups were reared at this <br />temperature. Between 50 and 100 fish from <br />each experimental group were transferred to <br />aquaria maintained at experimental (10 C, 14 <br />C) and control (20 C) temperatures. <br />Fish (n = 5-23 unless fewer fish remained on <br />last sampling date) were sampled from each <br />aquarium by fine-meshed dip net and weighed <br />and measured [total length (TL)]. Because of a <br />limited availability of G. CYPha, an attempt was <br />made to return individuals to experimental <br />aquaria alive following collection of data. Gila <br />CYPha were anesthetized in 125 mg/L MS-222, <br />placed on blotter paper for 5 sec, weighed and <br />measured, and returned to respective aquaria. <br />Age 7-day and age 14-day G. CYPha groups were <br />weighed to the nearest 0.1 mg and measured to <br /> <br />the nearest 0.1 mm; fish in the age 41-day G. <br />CYPha group were weigbed to the nearest 0.01 g. <br />Samples of P. lucius, C. latipinnis, and X. tex- <br />anus were sacrificed and preserved in 10% for- <br />malin prior to collection of length and weight <br />data (no corrections for shrinkage). Fish were <br />blotted 5 sec and weighed (nearest 0.1 mg) and <br />measured (nearest 0.1 mm). <br /> <br />Development.-We microscopically examined all <br />preserved specimens of C. latipinnis and X. tex- <br />anus to determine transformation from larval to <br />juvenile stages. For X. texanus and C. latipinnis, <br />D. E. Snyder and R. Muth (unpubI.) reported <br />that total lengths at loss of the preanal finfold <br />coincided with lengths at transformation, and <br />rarely were finfolds lost without concomitant ac- <br />quisition of the adult complement of fin rays. <br />We therefore used presence/absence ofthe pre- <br />anal finfold as the single determinant of life <br />stage. For G. CYPha and P. lucius, we considered <br />total lengths at loss of finfolds (D. E. Snyder, <br />unpubl.) as representative of size at transfor- <br />mation. We assessed time to transformation for <br />these species by comparing experimental repli- <br />cate mean lengths to D. E. Snyder's (unpubI.) <br />reported lengths at loss of finfolds. <br /> <br />Temperature shock.-Thermal-shock experiments, <br />to simulate conditions experienced by fishes en- <br />tering cold tailwaters from warm tributaries, <br />were conducted on young G. CYPha (5-7-dayand <br />11-13-day posthatch), X. texanus (7-9-day, 11- <br />13-day, and 42-43-day posthatch), and C. latipin- <br />nis (7-8-day, 14-15-day, and 42-43-day post- <br />hatch). Culture and rearing were as described <br />for growth experiments. Fishes were acclimated <br />to 20 C water over 24 h. One to three replicates <br />of 20-100 fish each were then transferred sep- <br />arately to aquaria at the following temperatures: <br />10 ::!:: 0.5 C, 12 ::!:: 0.5 C, and 14 ::'::: 0.5 C. Rep- <br />licate controls at 20 ::!:: 0.5 C for all groups were <br />handled in like manner. Fish behavior was ob- <br />served intensively for several minutes following <br />initiation of each treatment and thereafter for <br />I-min periods at various intervals over 1-5 h. <br /> <br />Analyses.- The Levene test determined that var- <br />iances of length and weight data (and transfor- <br />mations) within species-age-temperature groups <br />were not homogeneous. We employed the non- <br />parametric Kruskal-Wallis (K-W) test to com- <br />pare mean ranks of untransformed lengths and <br />weights across experimental temperatures for <br />each species and age group at each sampling <br />date. Significance levels were adjusted for mul- <br />tiple tests with the Bonferroni sequentially re- <br />jective multiple test procedure of Holm (1979). <br /> <br />"'" <br />