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<br />. <br /> <br />a" <br />, <br /> <br />, <br /> <br />198 <br /> <br />COMMUNICATIONS <br /> <br />drained by a surface standpipe. Water exchange <br />in breeder baskets was through the basket bottom <br />and sides. <br />Each of the test diets was fed to triplicate lots <br />of fish for 40 d (until the fish were 45 d old). The <br />five diets were AP-I00 (Zeigler Brothers, Inc., <br />Gardners, Pennsylvania), UV (Farm and Wildlife <br />Products, Inc., Omaha, Nebraska), 4200 (Bio-Ma- <br />rine, Hawthorne, California), and A-250 and B-250 <br />(BioKyowa, Inc., SL Louis, Missouri). All diets <br />were subjected to proximate analysis according to <br />standard methods (AOAC 1984). In addition, we <br />determined relative particle sizes by sieving 1.0- <br />g subsamples through three sizes of Nit ex. nylon <br />bolting cloth: 102, 153, and 243 ILm mesh (Wild- <br />life Supply Company, Saginaw, Michigan). Diets <br />were sieved three times by shaking, except LIV, <br />for which a small brush was used to preak up <br />clumps of this fine-grained food. <br />Fish were hand-fed at 5% of their body weight <br />per day. Food was divided into eight feedings per <br />day Monday-Friday and six feedings per day Sat- <br />urday and Sunday. A subsample of fish was <br />weighed with an electronic balance (sensitivity, <br />zO.OI g) at the initiation ofthe study to determine <br />daily feeding rate. Fish were not weighed during <br />trials for feeding rate adjustment, because addi- <br />tional handling of the small fish could have in- <br />creased mortality and thus confounded treatment <br />effects. Tanks and breeder baskets were cleaned <br />by siphoning, and fish deaths were recorded daily. <br />All fish were removed from each basket after <br />40 d and weighed as a group. The largest and <br />smallest individuals in each replicate were mea- <br />sured (TL) to determine size range. The stated size <br />of fish for each treatment was obtained by sum- <br />ming the lengths of the large and small individuals <br />for the three replicates and using the resultant av- <br />erage. The size range for each treatment was the <br />absolute range among replicates. Survival and av- <br />erage weights were compared by one-way analysis <br />of variance (ANOV A) and Duncan's multiple- <br />range test. Analysis of covariance (ANCOV A) was <br />used to compare weight gain with survival within <br />diets (Sokal and Rohlf 1981). Tests of significance <br />were not performed on total length data. <br /> <br />Results and Discussion <br />Growth and Survival <br /> <br />Diets A-250 and 4200 produced the highest <br />weight gain (0.092 and 0.066 g, respectively) but <br />the lowest survival (32 and 20%, respectively; Ta- <br />ble 1), and diets UV and B-250 produced the <br /> <br />",. <br /> <br />'. <br /> <br />highest survival (78%) but the lowest weight gains <br />(0.026 and 0.031 g, respectively; Table 1). Diet <br />AP-loo was intermediate for both weight gain <br />(0.036 g) and survival (59%; Table 1). Fish density <br />(survival to 45 d of age) had no discernible effect <br />on average weight gain within diets (ANCOV A, <br />P = 0.36). However, fish density had a weak in- <br />verse relationship with weight gain when all diets <br />were combined (r = -0.67, P < 0.01). Papoulias <br />(1988) found that razorback sucker larvae held at <br />150C experienced a 10% mortality rate if not fed <br />by 11 d after hatch, and this rate increased to 93% <br />if the fish were not fed until 31 d after hatch. We <br />assumed that fish in our study that survived 40 d <br />were accepting feed, and that the diff'erences in <br />survival were due to the diets. <br />Fish size at completion of the study (range, 11- <br />27 mm TL; average, 18.3 mm) waseomparable <br />to that obtained with live nauplii of brine shrimp <br />(Artemia salina). Papoulias (1988) reported sur- <br />vivors that were 11.8-28.8 mm TL (six trials; av- <br />erage, 18.8 mm TL) for larvae fed brine shrimp <br />for 50 d. In trials with abundant food (50-1,311 <br />naupllilfish daily), fish survival was high (80-93%) <br />and average fish size was 21 mm TL (Papoulias <br />1988). We presume that our ration was limiting <br />and that better growth would have resulted had <br />more food been available to the larvae. Although <br />the initial ration was 5% of body weight per day, <br />the average ration at completion of the study <br />ranged from 0.9 to 2% of body weight per day for <br />the different diets. <br /> <br />Proximate Composition and Particle Size <br /> <br />The five closed-formula diets varied in proxi- <br />mate analysis and particle size (Table 2). All diets <br />had similar protein content (range 49.8-57.0%) <br />but varied in fat content (range 6.4-30.2%). The <br />two diets producing the highest survival (LIV and <br />B-250) diff'ered in fat content and dry particle size. <br />The UV diet had a higher fat content (30.2%) and <br />smaller particles (average size, 50 ILm;. all < 102 <br />ILm), and B-250 had lower fat (14.6%) and larger <br />particles (average, 240 ILm; 87% > 153 ILm). How- <br />ever, both diets had a ftourlike consistency. Diets <br />A-250 and 4200, which produced the largest weight <br />gains but lowest survivals, had different amounts <br />of fat (20.1 and 6.4%, respectively); both diets <br />consisted of larger particles (averages, 284 and 185 <br />ILID, respectively). <br />We hypothesized that fish growth and survival <br />could be associated with diet particle size. How- <br />ever, a regression of dry particle size with fish <br />survival and growth (r = -0.36, P = 0.19 for <br /> <br />