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? .Y <br />f <br />2 <br />arranged in rows in raceways. Jars were placed in series, (not <br />randomly), with position effects controlled by a constant <br />temperature water bath and providing uniform lighting. <br />Continuous water flow at approximately 100 ml/min and constant <br />volume were provided by 2.54-cm pvc pipes perforated above each <br />aar. Jars were tiltad to facilitate outflow and screened with <br />fine mesh to prevent escape of larval fish and live food. <br />On 11 February 1985, adult male and female wild-caught (Lake <br />Mohave) razorback suckers were infected with human chorionic <br />gonadotropin. Three days later, fish were stripped and <br />fertilized eggs incubated at 210C in Heath trays (R. Hammond, <br />pers. comm.). Hatching occurred from 19 through 21 February and <br />swim-up on 23 February. On 25 February, 10 mm total length (TL) <br />larvae were stocked at 10 individuals per ,far. Experiments were <br />continued for 50 days, until 16 April, at a constant temperature <br />of 180C. <br />Fish selected for feeding received newly-hatched brine <br />shrimp (Artemis saline) nauplii. San Francisco BayR brand eggs <br />were incubated in aerated gallon bars at 27-28oC for 36 hours, at <br />which time most had hatched. Jars were agitated and allowed to <br />sit for 1/2 hour, during which time unhatched eggs floated to the <br />surface and nauplii accumulated near bottom. The latter were <br />siphoned to a glass beaker. Density estimates were by 5 counts <br />in a Sedgewick-rafter cell on 1 ml aliquots. Appropriate amounts <br />were then removed and prepared by dilution for various levels of <br />feeding. Fish were fed 3 times a day at 8-hour intervals. Jars