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Can we obtain monosex sea bass populations through selective breeding?

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HAL Id: hal-01001399

https://hal.archives-ouvertes.fr/hal-01001399

Submitted on 3 Jun 2020

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Can we obtain monosex sea bass populations through selective breeding?

Marc Vandeputte, Mathilde Dupont-Nivet, Pierrick Haffray, H. Chavanne, A. Vergnet, Edwige Quillet, B. Chatain

To cite this version:

Marc Vandeputte, Mathilde Dupont-Nivet, Pierrick Haffray, H. Chavanne, A. Vergnet, et al.. Can we obtain monosex sea bass populations through selective breeding?. 62. Annual Meeting of the European Association for Animal Production (EAAP), Aug 2011, Stavanger, Norway. pp.328. �hal-01001399�

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Material and methods

Context

Vandeputte, M.

1,2

, Dupont-Nivet, M.

1

, Haffray, P.

3

, Cha

I1INRA, UMR1313 GABI, Domaine de Vilvert, 78350 Jouy en Josa Palavas les Flots, France, 3Sysaaf, Campus de Beaulieu, 35000 R

Emplacement photo  qualité 150dpi minimum Emplacement photo  qualité 150dpi minimum Emplacement photo  qualité 150dpi minimum

Can we obtain monosex sea bass po

In the European sea bass, the sex-ratio of farm male-biased (> 75%), while wild populations se ratio. Females are preferred by farmers due to The situation in farmed populations is known larval rearing temperature, but also to genetic polygenic, and linked with growth rate. We tes and phenotypic selection for growth on popula genetics framework where phenotypic sex is m an underlying liability called “sex tendency” genetic and environmental effects.

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 Mâles Femel les 33 wild ♂ (W) 23 wild ♀ G0 G1 n=5915 longueur Selection threshold

12

e

Séminaire des thésards du Départemen

INSTITUT NATIONAL DE LA RECHERCHE AGRONOMIQUE / Ifremer GDR Amélioration génétique pour une Pisciculture Durable

Chemin de Maguelone, 34250 Palavas-les-Flots

Tél : +33(4) 67 13 04 07 • Courriel : marc.vandeputte@jouy.inra.fr

Results

62

nd

EAAP Annual Meeting, Stavanger, N

G2

13 femelles

20 mâles Sauvages

20 mâles

Domest. (G1) 20 mâles Massal

1. 18.2% females in G1, h²=0.62 for sex tendency, h²=0 body length, rA=0.48

2. Body weight in G2: S>D=W, +15 to 20% for S

3. Sex-ratio in G2: S 58.4%♀, D 47.1%♀, W 41.4%♀ (P<0. 4.Simulation: 75% females in G10 if the 5% largest fi selected at each generation (fig2). If those G10 fish were in conditions mimicking the natural ones, 95% females be expected

Conclusions

1. Selection for body length induces a correlated res on sex-ratio, with more females in growth-selected fish

2.Combining selection for growth and manipulati environmental conditions should allow the product quasi-monosex populations of sea bass for aquaculture.

n=1098

avanne, H.

4

, Vergnet, A.

2

, Quillet, E.

1

and Chatain, B.

2

as, France, 2Ifremer UMR110 INTREPID, Chemin de Maguelone, 34250 Rennes, France, 4ISILS, Localita la Quercia, 26027 Rivolta d Adda, Italy

opulations through selective breeding ?

med populations is usually highly eem to conform to a 50/50 sex better growth and later puberty. to be linked to larval and post-c fapost-ctors whipost-ch are presumably sted the impact of domestication ation sex-ratio, in a quantitative modeled as a threshold trait with ”, which is influenced both by

1.Factorial mating design with 33 wild G0♂ (W), 23 W♀ 7000 offspring individually tagged at 35 g (1 year), parentage assignment by genotyping of microsatellites(>98%), phenotyping of G1 at 400g (2 yrs) for sex & growth

2. Estimation of genetic parameters of growth & sex (h2, r

A) in

G1 fish by covariance between relatives (REML)

3. experimental selection for growth on G1 fish, P=5% on body length (BL)Î20 S males, + 20 males with average body length (D= domesticated)

4. Evaluation of response to selection and domestication on body weight and sex-ratio (20 W D and S males mated to 13

Figure 1:  The threshold model for sex‐ratio  in sea bass, with the phenotypic effect of early rearing environment in farms. 20%F 80% M sex tendency male-female threshold 50% F 50%M in the wild captive

nt de Génétique Animale Pornichet, 6 & 7 avril 2010

body weight and sex ratio (20 W, D and S males mated to 13 standard wild females)

5. Stochastic simulation study of selection on body length (quantitative genetics framework, h²=0.41 for body length, 0.62 for sex tendency, genetic correlation = 0.48) & estimation of the correlated response on sex-ratio.

Norway - 29 August - 1 September 2011

0.41 for .001) ish are reared would sponse ion of tion of Acknowledgements

This work was conducted in the frame of two European projects, Heritabolum (Q5CR‐2002‐71720) and Competus (COOP‐CT‐2005‐017633). It is also part of the work programme of the INRA‐Ifremer Research Group on Sustainable Fish Breeding.

Figure 3: Simulated co‐evolution of body length and sex‐ratio in a  population of sea bass submitted to phenotypic selection on body  length with a proportion selected of 5% at each generation 0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 150 200 250 300 350 400 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 P ropor ti on  of  fe m al e s Bo d le n gth  (mm) Generations

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