production and nutritional adaptation of the brine shrimp artemia sp. as live food organism for larvae of marine cold water fish species

PhD Thesis by Jan Ove Evjemo


Norwegian University of Science and Technology, Faculty of Chemistry and Biology, Trondheim, Norway, 2001,

ISBN: 82-471-5050-6

 

Conclusions:

A. franciscana feeding on different concentrations of algae increased the ingestion rate as a function of food concentration up to a saturating level. Further increase of the food concentration did not effect the ingestion rate. Different stages of A. franciscana showed a type 3 functional response.

The assimilation rate of A. franciscana was high at saturated food concentrations (10-15 mg C/l) and decreased at higher concentrations of algae (20 and 30 mg C/l). Assimilation efficiency (%) was high at low food concentrations and decreased at higher concentrations.

The growth rate of A. franciscana reached an optimum at saturated food concentrations. At lower concentrations the growth decreased successively as a function of algal concentration. A. franciscana, fed saturated food concentrations, showed significantly changes of the growth rate when the animals developed from nauplii the adult stage. In the exponential part the growth cycles the individual dry weight might increase from 2 until 3 times per 24 h. Based on these results there is a wide range of possibilities to manipulate the size of A. franciscana and thereby provide the most ideal size of the live food organism for the fist larvae.

DHA accumulates at a high rate during enrichment of A. franciscana but the high loss rate of DHA after enrichment might be a problem. It is important to establish careful routines post enrichment that allow transfer of A. franciscana to the fish tanks shortly after enrichment. Short residence time of the live food in the fish tanks will reduce DHA catabolism. If A. franciscana must be stored this should take place at a relatively low temperatures (<6°C).

The loss rates of the lipid and protein content after enrichment increased with increasing temperature. The total lipid content decreased at a higher rate than the protein content and DHA became reduced at a considerably higher rate than EPA. The nutritional value of A. franciscana might be significantly reduced when residence time between end of enrichment and larval consumption increase.

The non-commercial Chinese strain, Artemia sinica, retained a high DHA level post enrichment and was less affected by the temperature than A. franciscana. This might indicate that the catabolism of DHA is genetically determined.

The total protein content in Artmeia sp. might be at an acceptable level for marine fish larvae of the cold water fish species, whereas the lipid level must be modified through enrichment with emulsified lipids.

There were significant differences in the lipid content and the distribution of fatty acids in the marine copepods examined and enriched A. franciscana. The copepods were characterised by a relatively low lipid content and a high content of n-3 HUFA. A.franciscana had higher lipid content and a lower n-3 HUDA content. Through proper enrichment diets the n-3 HUFA content in A. franciscana can be significantly increased. By introducing new enrichment diets, particularly developed for Artemia sp. when used as live food organism for marine cold water fish species, the nutritional value of Artemia sp. might reach the requirements of the fish larvae.

There was a close relationship between the percent DHA content in the halibut larvae and in different live food organisms fed to the larvae. High DHA content in the live food organism was reflected by a high DHA content in the larvae and vice versa. The DHA content in the larvae was significantly reduced after 8 days of feeding when the live food organisms used had a relatively low DHA content.

 

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