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<br />COMMUNICATIONS
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<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
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<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
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