|Impact of the supplementation of a docosahexaenoic acid-rich emulsion on the reproductive output of oyster broodstock, Crassostrea gigas|
Caers, M.; Utting, S.D.; Coutteau, P.; Millican, P.F.; Sorgeloos, P. (2002). Impact of the supplementation of a docosahexaenoic acid-rich emulsion on the reproductive output of oyster broodstock, Crassostrea gigas, in: (2002). VLIZ Coll. Rep. 32(2002). VLIZ Collected Reprints: Marine and Coastal Research in Flanders, 32: pp. chapter 5
In: (2002). VLIZ Coll. Rep. 32(2002). VLIZ Collected Reprints: Marine and Coastal Research in Flanders, 32. Flanders Marine Institute (VLIZ): Oostende, more
In: VLIZ Collected Reprints: Marine and Coastal Research in Flanders. Vlaams Instituut voor de Zee: Oostende. ISSN 1376-3822, more
|Also published as |
- Caers, M.; Utting, S.D.; Coutteau, P.; Millican, P.F.; Sorgeloos, P. (2002). Impact of the supplementation of a docosahexaenoic acid-rich emulsion on the reproductive output of oyster broodstock, Crassostrea gigas. Mar. Biol. (Berl.) 140(6): 1157-1166. dx.doi.org/10.1007/s00227-002-0798-5, more
Brood stocks; Food additives; Oyster culture; Crassostrea gigas (Thunberg, 1793) [WoRMS]; Marine
|Authors|| || Top |
- Caers, M., more
- Utting, S.D.
- Coutteau, P., more
- Millican, P.F.
- Sorgeloos, P., more
Pacific oyster [Crassostrea gigas (Thunberg)] broodstock were hatchery-conditioned with either a mixed algal diet of Dunaliella tertiolecta, Tetraselmis suecica and Rhodomonas sp. [1:1:1, on a dry weight (DW) basis] (Control), a single diet of D. tertiolecta (Duna) or a single diet of D. tertiolecta supplemented with an emulsion rich in eicosapentaenoic (20:5n-3) and particularly docosahexaenoic acid (22:6n-3) (Duna+Em). Oysters were spawned after a conditioning period of 7 and 8 weeks and larvae were reared for 1 week on an Isochrysis galbana (clone T-Iso) diet. The percentage recovery of D-larvae from eggs of Control-fed oysters and Duna+Em-fed oysters was not significantly different (80% and 63% after 7 weeks of conditioning; 87% and 74% after 8 weeks of conditioning, respectively] but was much higher than from eggs produced by Duna-fed oysters (24% and 41% after 7 and 8 weeks of conditioning, respectively). A reduction in the percentage recovery of D-larvae as a result of temperature or salinity stress was most severe in eggs from Duna-fed oysters. Neither the broodstock diet nor the conditioning period affected the size of eggs or D-larvae, larval performance, or lipid content and lipid class distribution of the eggs. The fatty acid composition of the eggs was modified by the fatty acid composition of the algal diet and the lipid emulsion. The supplementation of the emulsion resulted in a pronounced increase in the percentage of 22:6n-3 in the polar (PL) and neutral lipids (NL) of the eggs (4.0-13.4% and 8.5-14.7% in NL and PL, respectively). The egg lipids (7-8 ng egg-1) contained about 62% NL and were dominated by triglycerides (TAG), which made up 65% of the NL. The major phospholipids were phosphatidylethanolamine (PE), ceramide aminoethylphosphonate and phosphatidylinositol (CAEP+PI), phosphatidylserine (PS) and phosphatidylcholine (PC). Regardless of the broodstock diet treatment, the PL fraction contained high percentages of non-methylene-interrupted dienes (NMID) and plasmalogens (detected as dimethyl acetals).