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11cperiments were performed indoors at Dexter National Fish <br />Hatchery (NM, Dexter, New Mexico. One gallon (3.9 L) glass jars <br />were arranged in rows in raceways. Jars were placed in series (not <br />randomly), with position effects controlled by a constant-twperature <br />water bath and providing uniform lighting. Continuous water flow at <br />approxfmately 100 ml min 7l and constant volume were provided by 2.54- <br />cm pipes perforated above each jar. Jars were tilted to facilitate <br />outf o 1t and screened to Prevent escape of larval fish and live food. <br />Adult, wild-caught (Lake Mohave) female razorback suckers <br />received three injections of 220 N chorionic gonadotrcpin kg-l body <br />weight at 24-h intervals for 3 d begi tini ng 11 February 1985 (Ham¢nan <br />1985). Twenty--four h after the third injection, eggs could be <br />expelled with slight pressure. Gametes were then stripped, and <br />fertilized by milt from naturally-ripened, Jake Mohave males. <br />Fertilized eggs were incubated at 2100 in Heat trays (Inslee 1982). <br />Hatching began on 18 February, and larvae began to swim actively on 23 <br />February 1985. On 25 February, 9.4- to 10.7-mm TL (x = 9.96±0.04, <br />W50) larvae were stocked at 10 individuals jar 1. Mcperiments were <br />continued for 50 d, Until 16 April 1985, at a constant temperature of <br />18oC. <br />Larval fish randcamly selected for feeding trials received newly- <br />hatched, live brine shrimp (Artemia saliva) nauplii. San Francisco <br />BaYS brand eggs were incubated in aerated 3.9-L jars at 27-280C for 36 <br />8 <br />