A method for radiolabeling Artemia with applications in studies of food intake, digestibility, protein and amino acid metabolism in larval fish


S. Morais, L.E.C. Conceição, M.T. Dinis, I. Rønnestad-2004
Aquaculture, 231(1-4): 469-487

Abstract:

The present paper describes a method for radiolabeling Artemia that has potential applicability in the study of food intake, Artemia digestibility, protein and amino acid (AA) metabolism in early stages of marine fish larvae. Artemia nauplii were labeled by adding a uniformly labeled 14C protein hydrolysate to its hatching or enrichment media. Both newly hatched and enriched nauplii assimilated rapidly the radiolabel and a very high proportion of the uptaken label was incorporated into the TCA precipitate (mostly protein) fraction after a short period of time––84–91%, at the end of the hatching period and 81–87%, after 12 h of enrichment. In addition, it was observed that the amount of radiolabel per Artemia, as well as its distribution between the TCA precipitate and soluble (free AA) fractions, was relatively stable (up to 8 h) in conditions simulating transfer to larval feeding tanks. During the radiolabeling trials a substantial amount of the total initial radioactivity in the media was not recovered at the end of the hatching or enrichment period (38% and 29%, respectively). An experiment was designed to study the release of the radiotracer into the atmosphere, as 14CO2. It was concluded that although the Artemia catabolism may be responsible for some release of the radiolabel into the atmosphere, bacterial activity in the enrichment media has a major impact, being responsible for the loss of 19.2% of the total initial radiolabel from the system. The digestibility and transfer rates of the labeled nutrients from Artemia to fish larvae was analysed "in vivo" by feeding radiolabeled newly hatched nauplii to herring (Clupea harengus) larvae and following the metabolic fate of the label. The results revealed a high digestibility (around 60%) of the Artemia, with 20% being retained in the body and 39% catabolised by the larvae, 24 h after feeding. The digestion process and subsequent absorption of the digested radiolabeled nutrients were quite rapid, given that 40% was recovered in the body only 2 h after feeding and 6% was found in the CO2 trap at this time.

(CCMAR, Universidade do Algarve, Campus de Gambelas, 8000-117, Faro, Portugal, e-mail: smorais@ualg.pt)


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