D. Perry, R. Mercaldo-Allen, C. Kuropat, J. B. Hughes
{"title":"Laboratory Culture of Tautog","authors":"D. Perry, R. Mercaldo-Allen, C. Kuropat, J. B. Hughes","doi":"10.1577/1548-8640(1998)060<0050:LCOT>2.0.CO;2","DOIUrl":null,"url":null,"abstract":"Abstract Spawning of field-captured adult tautog Tautoga onitis was accomplished under laboratory conditions. Natural spawning of tautog produced more viable embryos and larvae than did strip-spawning. Embryos were cultured to hatching and raised successfully through the larval stage to juveniles. Newly hatched larvae were fed protozoans from day 0 to day 6 posthatch, rotifers from day 2 to day 20 posthatch, and brine shrimp Artemia salina from day 7 to several months posthatch. Rotifers and brine shrimp were enriched with highly unsaturated fatty acids. Supplementing cultured foods with natural plankton enhanced larval survival. Slow flow-through green-water culture proved superior to static culture methods. Handling resulted in high larval mortality. Laboratory-cultured brine shrimp and a commercial food provided an adequate diet for juvenile tautog.","PeriodicalId":22850,"journal":{"name":"The Progressive Fish-culturist","volume":"107 1","pages":"50-54"},"PeriodicalIF":0.0000,"publicationDate":"1998-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Progressive Fish-culturist","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1577/1548-8640(1998)060<0050:LCOT>2.0.CO;2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
Abstract
Abstract Spawning of field-captured adult tautog Tautoga onitis was accomplished under laboratory conditions. Natural spawning of tautog produced more viable embryos and larvae than did strip-spawning. Embryos were cultured to hatching and raised successfully through the larval stage to juveniles. Newly hatched larvae were fed protozoans from day 0 to day 6 posthatch, rotifers from day 2 to day 20 posthatch, and brine shrimp Artemia salina from day 7 to several months posthatch. Rotifers and brine shrimp were enriched with highly unsaturated fatty acids. Supplementing cultured foods with natural plankton enhanced larval survival. Slow flow-through green-water culture proved superior to static culture methods. Handling resulted in high larval mortality. Laboratory-cultured brine shrimp and a commercial food provided an adequate diet for juvenile tautog.