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Constant long photoperiod inhibits the onset of the reproductive cycle in roach females and males

  • Imen Ben AmmarEmail author
  • Sylvain Milla
  • Yannick Ledoré
  • Fabrice Teletchea
  • Pascal FontaineEmail author
Article

Abstract

Photoperiod and temperature are commonly accepted as the determinant factors for the control of the reproductive cycle in freshwater fishes. However, this determining effect is dependent on fish species. While applying a constant long photoperiod has an inhibitory effect in some species, the same photoperiodic manipulation has a stimulating effect in others. In cyprinids, a decrease in temperature or photoperiod can induce the gonad recrudescence. However, in roach Rutilus rutilus an early spring spawner cyprinid, there is little knowledge about the cueing role of each environmental factor. The aim of this work was to study the effect of a constant long photoperiod on the gametogenesis in roach. Fish were kept under either naturally simulated photoperiod or artificial constant long photoperiod and sampled at three times: at the beginning of photoperiod decrease, at the beginning of temperature decrease, and at the end of temperature decrease. Morphological parameters (gonado-somatic, hepato-somatic, and viscera-somatic indexes), plasma sexual steroids, and proportion of gametogenesis stages were estimated at each sampling time. The results showed that a constant, long photoperiod exerted inhibitory effects on gametogenesis advancement in both females and males that could stem from decrease of sex steroid production. Roach displayed a similar response to photoperiodic manipulations to other early spring spawners like percids, such as European perch, yellow perch and pikeperch. These results clearly showed the cueing role of the photoperiod in the induction of the reproductive cycle in roach.

Keywords

Photoperiod manipulation Inhibition Onset of reproductive cycle Roach 

Notes

Acknowledgments

We would like to thank all members of the AFPA research unit for their active collaboration in this study. We would also like to thank Julien Ruelle and Maryline Harroué from UMR 1092 AgroParisTech INRA Laboratoy of study of forest and wood resources “LERFoB”, technical platform xylosciences for the provision of the necessary equipment to realize the histological analyses (Technical Platform of functional ecogenomics, INRA Champenoux, France). We are thankful to Daniel Van Vlaender (Facultés Universitaires Notre-Dame de la Paix FUNDP, Belgium) for his help with histological protocols, Jos Fey (Faculty of Kinesiology and Rehabilitation Science, University of Leuven), Marie Fernandez (University of Saint Etienne, France) for their advices about statistics with R software, and Mark Holmes (University of Namur, Belgium) for the proofreading.

Funding information

This study was partly funded by the Tunisian Ministry of Higher Education and Research.

Supplementary material

10695_2019_698_MOESM1_ESM.docx (3.5 mb)
ESM 1 (DOCX 3537 kb).

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© Springer Nature B.V. 2019

Authors and Affiliations

  1. 1.Equipe Domestication en Aquaculture Continentale, UR AFPA–INRA, Faculté des SciencesUniversité de LorraineVandœuvre-lès-NancyFrance
  2. 2.Unité de Recherche en Biologie environnementale et évolutive, URBEUniversité de NamurNamurBelgique

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