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Peut-on utiliser l’ADN environnemental pour le suivi quantitatif des populations de poissons migrateurs ? Association LOGRAMI http://zotero.org/users/237438 http://zotero.org/users/237438/items/7WSDQ34Z 2025-05-22T07:31:57Z 2025-05-22T07:31:57Z 7WSDQ34Z 23408 journalArticle Quéméré et al. 2025-05-13 1
Item Type Journal Article
Author Erwan Quéméré
Author Zoé Raphalen
Author Anne-Laure Besnard
Author Marine Vautier
Author Natacha Nikolic
URL https://revue-set.fr/article/view/8475
Rights Copyright (c) 2025 Erwan QUÉMÉRÉ, Zoé RAPHALEN, Anne-Laure BESNARD, Marine VAUTIER, Natacha NIKOLIC
Issue 47
Pages 8475-8475
Publication Sciences Eaux & Territoires
ISSN 1775-3783
Date 2025-05-13
Extra Number: 47
DOI 10.20870/Revue-SET.2025.47.8475
Accessed 2025-05-22 07:31:57
Library Catalog revue-set.fr
Language fr
Abstract Amphihaline migratory fish are facing alarming declines due to anthropogenic and environmental pressures. In this context, environmental DNA (eDNA) emerges as a promising non-invasive approach to complement traditional population monitoring methods. We developed and validated species-specific genetic markers that enable the unambiquous detection and identification of five iconic migratory fish species (brown trout, Atlantic salmon, sea lamprey, European eel, and Alosa spp.). The aim was to assess whether the eDNA detected in water could reliably reflect the abundances measured at river counting stations. The results show effective detection for certain species and contexts but with significant variability depending on the markers and environmental conditions (temperature, turbidity, flow). For example, in the Adour River, peaks in eDNA concentrations were observed a few weeks after the migration peaks of trout and Alosa spp. Water temperature appears to play a major role in the release and persistence of eDNA, with optimal eDNA concentrations obtained at intermediate temperature ranges (around 18°C). In contrast, flow variations, especially in spring, seem to reduce species detectability due to eDNA dilution. This study represents an important step in integrating eDNA as a complementary tool to traditional monitoring methods for amphihaline migratory fish, particularly for species that are poorly documented at the national level. However, the complexity of the transport and degradation processes of DNA in aquatic environnements - still only partially understood - and the significant variability between river systems, call for continued research over several years to optimize sampling and analysis protocols, and to accurately integrate environmental parameters into reliable predictive models.

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