Publisert 2008

Les på engelsk


Tidsskrift : Aquaculture , vol. 274 , p. 232–240–9 , 2008

Utgiver : Elsevier

Internasjonale standardnummer :
Trykt : 0044-8486
Elektronisk : 1873-5622

Publikasjonstype : Vitenskapelig artikkel

Bidragsytere : Holtsmark, Marte; Klemetsdal, Gunnar; Sonesson, Anna Kristina; Woolliams, John Arthur

Sak : 2-4

Har du spørsmål om noe vedrørende publikasjonen, kan du kontakte Nofimas bibliotekleder.

Kjetil Aune


Guidelines for constructing base populations in fish were examined using a drift model. A large number of drift differentiated, wild subpopulations, with inbreeding F-wild (F-wild is an element of [0.05-0.20]), and a trait with heritability h(tot)(2) (h(tot)(2) is an element of [0.10-0.30]), were assumed. A base population was generated by sampling 2N fish from each of nsub subpopulations (nsub is an element of[1-8]), and then mated to produce 160 or 240 families per generation. The matings were either at random, in a structured diallel-cross, or within subpopulations to produce generation 1. Optimal contribution selection on phenotype was applied from generation 1 to 11, with a rate of inbreeding of 0.5% per generation. Genetic gain (Delta g) improved with nsub, the improvement being largest when going from one to two subpopulations, with diminishing returns. Most of the potential Initial matings across subpopulations improved Delta g from improvement was obtained with nsub=4, and was well predicted by Delta g(nsub)/Delta g(1) approximate to (1-F-wild/nsub)/(1-F-wild) the second round of selection compared to within. Consequently the effect of the mating strategy were first observed 3 generation after decisions were made and persisted over subsequent generations, but with minimal effect on the accumulated additive genetic gain in generation 11. It was concluded that sampling from at least four subpopulations was beneficial and that mating across subpopulations should start as early as possible. (c) 2007 Elsevier B.V. All rights reserved.