Food Quality and Life‐History Genotype Influence Maturation and Reproductive Traits in Female Atlantic Salmon

Author:

Maamela Katja Susanna123ORCID,Åsheim Eirik Ryvoll1234ORCID,O'Sullivan Ronan James15ORCID,Debes Paul Vincent126ORCID,House Andrew Herbert123ORCID,Liljeström Petra13,Prokkola Jenni Maria17ORCID,Niemelä Petri Toivo1ORCID,Erkinaro Jaakko7ORCID,Mobley Kenyon Brice18ORCID,Primmer Craig Robert12ORCID

Affiliation:

1. Organismal and Evolutionary Biology Research Program, Faculty of Biological and Environmental Sciences University of Helsinki Helsinki Finland

2. Institute of Biotechnology Helsinki Institute of Life Science, University of Helsinki Helsinki Finland

3. Lammi Biological Station, Faculty of Biological and Environmental Sciences University of Helsinki Lammi Finland

4. Institute of Freshwater Research, Department of Aquatic Resources Swedish University of Agricultural Sciences Drottningholm Sweden

5. Faculty of Physiology and Genetics, Department of Biology University of Turku Turku Finland

6. Department of Aquaculture and Fish Biology Hólar University Sauðárkrókur Iceland

7. Natural Resources Institute Finland Oulu Finland

8. Norwegian College of Fishery Science The Arctic University of Norway Tromsø Norway

Abstract

ABSTRACTAge at maturity is an important life‐history trait, often showing sex‐specific variation, contributing to life‐history diversity in many species. Atlantic salmon ( Salmo salar ) are an excellent model system to investigate genetic and environmental factors affecting sex‐specific maturation, yet few laboratory studies have focused on females as they mature later than males, on average. Using a 4‐year common‐garden experiment of Atlantic salmon, we assessed the influence of diet (low‐fat vs. control) and vgll3 (a candidate gene influencing maturation age) on maturation and related phenotypic traits of female Atlantic salmon derived from two second‐generation hatchery populations. We found the early‐maturation associated E allele to be additively associated with a higher probability of maturation. Heritability of maturation was estimated to be 0.295, with vgll3's contribution to phenotypic variance being ~2%. In addition, body condition measured in the spring prior to spawning influenced maturation. Body condition, in turn, was influenced by population and diet. The more northern Oulu population and the low‐fat diet were associated with lower body condition compared to the more southern Neva population and the control diet. Moreover, there was an interaction between population and diet on body condition, suggesting that populations may respond differently to nutrient availability. These results broaden our understanding of the processes underlying sex‐ and population‐specific maturation and demonstrate that genes and environment influence age at maturity in a species that displays sex‐specific variation in maturation.

Funder

Academy of Finland

Societas pro Fauna et Flora Fennica

H2020 European Research Council

Suomen Kulttuurirahasto

OLVI-Säätiö

HORIZON EUROPE European Research Council

Publisher

Wiley

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