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Environmental DNA for freshwater fish monitoring: insights for conservation within a protected area

BACKGROUND: Many fish species have been introduced in wild ecosystems around the world to provide food or leisure, deliberately or from farm escapes. Some of those introductions have had large ecological effects. The north American native rainbow trout (Oncorhynchus mykiss Walbaum, 1792) is one of t...

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Autores principales: Fernandez, Sara, Sandin, Miguel M., Beaulieu, Paul G., Clusa, Laura, Martinez, Jose L., Ardura, Alba, García-Vázquez, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844247/
https://www.ncbi.nlm.nih.gov/pubmed/29527421
http://dx.doi.org/10.7717/peerj.4486
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author Fernandez, Sara
Sandin, Miguel M.
Beaulieu, Paul G.
Clusa, Laura
Martinez, Jose L.
Ardura, Alba
García-Vázquez, Eva
author_facet Fernandez, Sara
Sandin, Miguel M.
Beaulieu, Paul G.
Clusa, Laura
Martinez, Jose L.
Ardura, Alba
García-Vázquez, Eva
author_sort Fernandez, Sara
collection PubMed
description BACKGROUND: Many fish species have been introduced in wild ecosystems around the world to provide food or leisure, deliberately or from farm escapes. Some of those introductions have had large ecological effects. The north American native rainbow trout (Oncorhynchus mykiss Walbaum, 1792) is one of the most widely farmed fish species in the world. It was first introduced in Spain in the late 19th century for sport fishing (Elvira 1995) and nowadays is used there for both fishing and aquaculture. On the other hand, the European native brown trout (Salmo trutta L.) is catalogued as vulnerable in Spain. Detecting native and invasive fish populations in ecosystem monitoring is crucial, but it may be difficult from conventional sampling methods such as electrofishing. These techniques encompass some mortality, thus are not adequate for some ecosystems as the case of protected areas. Environmental DNA (eDNA) analysis is a sensitive and non-invasive method that can be especially useful for rare and low-density species detection and inventory in water bodies. METHODS: In this study we employed two eDNA based methods (qPCR and nested PCR-RFLP) to detect salmonid species from mountain streams within a protected area, The Biosphere Reserve and Natural Park of Redes (Upper Nalón Basin, Asturias, Northern Spain), where brown trout is the only native salmonid. We also measured some habitat variables to see how appropriate for salmonids the area is. The sampling area is located upstream impassable dams and contains one rainbow trout fish farm. RESULTS: Employing qPCR methodology, brown trout eDNA was detected in all the nine sampling sites surveyed, while nested PCR-RFLP method failed to detect it in two sampling points. Rainbow trout eDNA was detected with both techniques at all sites in the Nalón River’ (n1, n2 and n3). Salmonid habitat units and water quality were high from the area studied. DISCUSSION: In this study, a high quantity of rainbow trout eDNA was found upstream and downstream of a fish farm located inside a Biosphere Reserve. Unreported escapes from the fish farm are a likely explanation of these results. Since salmonid habitat is abundant and the water quality high, the establishment of rainbow trout populations would be favored should escapes occur. Environmental DNA has here proved to be a valuable tool for species detection in freshwater environments, and the probe-based qPCR highly sensitive technique for detection of scarce species. We would recommend this method for routine monitoring and early detection of introduced species within natural reserves.
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spelling pubmed-58442472018-03-09 Environmental DNA for freshwater fish monitoring: insights for conservation within a protected area Fernandez, Sara Sandin, Miguel M. Beaulieu, Paul G. Clusa, Laura Martinez, Jose L. Ardura, Alba García-Vázquez, Eva PeerJ Aquaculture, Fisheries and Fish Science BACKGROUND: Many fish species have been introduced in wild ecosystems around the world to provide food or leisure, deliberately or from farm escapes. Some of those introductions have had large ecological effects. The north American native rainbow trout (Oncorhynchus mykiss Walbaum, 1792) is one of the most widely farmed fish species in the world. It was first introduced in Spain in the late 19th century for sport fishing (Elvira 1995) and nowadays is used there for both fishing and aquaculture. On the other hand, the European native brown trout (Salmo trutta L.) is catalogued as vulnerable in Spain. Detecting native and invasive fish populations in ecosystem monitoring is crucial, but it may be difficult from conventional sampling methods such as electrofishing. These techniques encompass some mortality, thus are not adequate for some ecosystems as the case of protected areas. Environmental DNA (eDNA) analysis is a sensitive and non-invasive method that can be especially useful for rare and low-density species detection and inventory in water bodies. METHODS: In this study we employed two eDNA based methods (qPCR and nested PCR-RFLP) to detect salmonid species from mountain streams within a protected area, The Biosphere Reserve and Natural Park of Redes (Upper Nalón Basin, Asturias, Northern Spain), where brown trout is the only native salmonid. We also measured some habitat variables to see how appropriate for salmonids the area is. The sampling area is located upstream impassable dams and contains one rainbow trout fish farm. RESULTS: Employing qPCR methodology, brown trout eDNA was detected in all the nine sampling sites surveyed, while nested PCR-RFLP method failed to detect it in two sampling points. Rainbow trout eDNA was detected with both techniques at all sites in the Nalón River’ (n1, n2 and n3). Salmonid habitat units and water quality were high from the area studied. DISCUSSION: In this study, a high quantity of rainbow trout eDNA was found upstream and downstream of a fish farm located inside a Biosphere Reserve. Unreported escapes from the fish farm are a likely explanation of these results. Since salmonid habitat is abundant and the water quality high, the establishment of rainbow trout populations would be favored should escapes occur. Environmental DNA has here proved to be a valuable tool for species detection in freshwater environments, and the probe-based qPCR highly sensitive technique for detection of scarce species. We would recommend this method for routine monitoring and early detection of introduced species within natural reserves. PeerJ Inc. 2018-03-06 /pmc/articles/PMC5844247/ /pubmed/29527421 http://dx.doi.org/10.7717/peerj.4486 Text en ©2018 Fernandez et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Aquaculture, Fisheries and Fish Science
Fernandez, Sara
Sandin, Miguel M.
Beaulieu, Paul G.
Clusa, Laura
Martinez, Jose L.
Ardura, Alba
García-Vázquez, Eva
Environmental DNA for freshwater fish monitoring: insights for conservation within a protected area
title Environmental DNA for freshwater fish monitoring: insights for conservation within a protected area
title_full Environmental DNA for freshwater fish monitoring: insights for conservation within a protected area
title_fullStr Environmental DNA for freshwater fish monitoring: insights for conservation within a protected area
title_full_unstemmed Environmental DNA for freshwater fish monitoring: insights for conservation within a protected area
title_short Environmental DNA for freshwater fish monitoring: insights for conservation within a protected area
title_sort environmental dna for freshwater fish monitoring: insights for conservation within a protected area
topic Aquaculture, Fisheries and Fish Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844247/
https://www.ncbi.nlm.nih.gov/pubmed/29527421
http://dx.doi.org/10.7717/peerj.4486
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