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<br />. REFERENCE NUMBER: <br />CITATION: <br /> <br />006 <br /> <br />Hamman. R.1.. 1981a. Spawning and culture of Colorado squawfisb <br />in raceways. Progressive Fisb-Culturist. 43(4):173-177. <br /> <br />SPECIES AND LIFE STAGE: <br /> <br />CS, CS_ADU, CS_EGG, CS_LAR <br /> <br />TOPICS: <br /> <br />ute History, Production, Culture Techniques, Temp, Diet, Water <br />Quality <br /> <br />COLORADO SQUA WFISH, BROODSTOCK, ARTIFICIAL <br />SPAWNING, NATURAL SPAWNING, SUBSTRATE, <br />FECUNDITY, PH, DISSOLVED OXYGEN, AMMONIA, <br />OVERCROWDING, TEMPERATURE FLUCIUATION <br /> <br />KEYWORDS: <br /> <br />. <br /> <br />SUMMARY: Brood stock consisting of 13 wild adults from the Colorado River between Grand Junction, <br />Colorado and Moab, Utah and 14 wild adults from tbe Green River between Ouray and <br />Jensen, Utah and two groups of hatchery reared fish were spawned at Dexter National FISb <br />Hatchery by several different techniques. One group of wild fish were allowed to spawn <br />naturally in a concrete raceway over substrate of boulders (30 - 40 em) and cobble (4 - 10 em) <br />water depth ranged from 10 - 76 em. Five wild females were injected with acetone-dried carp <br />pituitary (40 mg) in a solution of oxytetracycline hydrochloride (10 ml) and allowed to spawn <br />un-aided in a raceway with similar substrate. Thirty-nine hatchery reared females were injected <br />at 4 mg/kg body weight and 39 were injected at 8 mg/kg body weight. When eggs could be <br />expressed these fish were anesthetized and were stripped into plastic pans. Water diluted milt <br />from four males was added to these eggs which were then stirred for 45 min and water <br />bardened for 50 miD. Eggs were poured onto 53 x 53 em trays covered with 1.4 mm mesh <br />hardware cloth and angled 300 to an 811min flow and incubated at 20-210C or 12-130C. <br /> <br />Males began acquiring small tubercles on head, operculars and fins in late April at 150C and <br />had fully developed milt by June at 2ooC. Females showed no spawning characteristics until <br />June. Fecundity and survival of fry varied greatly among the treatments. Wild uninjected <br />females averaged 25,000 eggs from which 7,500 fry were hatched. Hatching began at 96 hand <br />took place over 48 h. Larvae were 6.5 - 7.0 mm TL. Fecundity of injected wild stock averaged <br />55,000 eggs from which 32,500 hatched naturally and 4,500 of 5,000 eggs incubated as described <br />above were hatched. Hatching began in the raceway at 90 h (22 - 240C) and was complete 40 <br />h later, hatching in trays began at 90 h and was complete 30 h later (20 - 210C). All larvae <br />ranged from 6.5 - 7.5 mm TL. Hatchery females owlated about 24 h after one injection and <br />produced 78,540 eggs or 10,542 eggs per kilogram of body weight. Survival however was low, <br />2,000 eggs (3%) hatched. Eggs incubated at 20 - 210C began hatching at 96 h and were <br />complete 25 h later, eggs incubated at 12 - 130C began hatching at 145 b and were complete <br />35 b later. No difference in egg fenility or fry survival was noted between the two water <br />temperatures. Fry were reared in previously fenilized recirculating systems held at 23 _ 240C. <br />Oa:asional temperature drops of 10000ver 10 min were tolerated by the fish. Also an oxygen <br />depletion from 9.9 mgIL down to 1.5 mgIL occurred causing only 60 monalities. <br /> <br />. <br /> <br />Injection of wild fish and subsequent spawning over natural substrate in a raceway was superior <br />in egg production and hatching success. Uninjected wild females had 30% hatching success, <br />injected wild females had 67% success and anificially' spawned hatchery females had 3% <br />hatching success. FISh were able to endure variable culture conditions including low dissolved <br />oxygen (1.5 mgIL), high ammonia nitrogen (2.0 mgIL), high carbon dioxide (15.0 mgIL), high <br />pH (9.0). <br /> <br />A-6 <br />