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Acidity promotes degradation of multi-species environmental DNA in lotic mesocosms

Accurate quantification of biodiversity is fundamental to understanding ecosystem function and for environmental assessment. Molecular methods using environmental DNA (eDNA) offer a non-invasive, rapid, and cost-effective alternative to traditional biodiversity assessments, which require high levels...

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Autores principales: Seymour, Mathew, Durance, Isabelle, Cosby, Bernard J., Ransom-Jones, Emma, Deiner, Kristy, Ormerod, Steve J., Colbourne, John K., Wilgar, Gregory, Carvalho, Gary R., de Bruyn, Mark, Edwards, François, Emmett, Bridget A., Bik, Holly M., Creer, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123786/
https://www.ncbi.nlm.nih.gov/pubmed/30271891
http://dx.doi.org/10.1038/s42003-017-0005-3
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author Seymour, Mathew
Durance, Isabelle
Cosby, Bernard J.
Ransom-Jones, Emma
Deiner, Kristy
Ormerod, Steve J.
Colbourne, John K.
Wilgar, Gregory
Carvalho, Gary R.
de Bruyn, Mark
Edwards, François
Emmett, Bridget A.
Bik, Holly M.
Creer, Simon
author_facet Seymour, Mathew
Durance, Isabelle
Cosby, Bernard J.
Ransom-Jones, Emma
Deiner, Kristy
Ormerod, Steve J.
Colbourne, John K.
Wilgar, Gregory
Carvalho, Gary R.
de Bruyn, Mark
Edwards, François
Emmett, Bridget A.
Bik, Holly M.
Creer, Simon
author_sort Seymour, Mathew
collection PubMed
description Accurate quantification of biodiversity is fundamental to understanding ecosystem function and for environmental assessment. Molecular methods using environmental DNA (eDNA) offer a non-invasive, rapid, and cost-effective alternative to traditional biodiversity assessments, which require high levels of expertise. While eDNA analyses are increasingly being utilized, there remains considerable uncertainty regarding the dynamics of multispecies eDNA, especially in variable systems such as rivers. Here, we utilize four sets of upland stream mesocosms, across an acid–base gradient, to assess the temporal and environmental degradation of multispecies eDNA. Sampling included water column and biofilm sampling over time with eDNA quantified using qPCR. Our findings show that the persistence of lotic multispecies eDNA, sampled from water and biofilm, decays to non-detectable levels within 2 days and that acidic environments accelerate the degradation process. Collectively, the results provide the basis for a predictive framework for the relationship between lotic eDNA degradation dynamics in spatio-temporally dynamic river ecosystems.
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spelling pubmed-61237862018-09-28 Acidity promotes degradation of multi-species environmental DNA in lotic mesocosms Seymour, Mathew Durance, Isabelle Cosby, Bernard J. Ransom-Jones, Emma Deiner, Kristy Ormerod, Steve J. Colbourne, John K. Wilgar, Gregory Carvalho, Gary R. de Bruyn, Mark Edwards, François Emmett, Bridget A. Bik, Holly M. Creer, Simon Commun Biol Article Accurate quantification of biodiversity is fundamental to understanding ecosystem function and for environmental assessment. Molecular methods using environmental DNA (eDNA) offer a non-invasive, rapid, and cost-effective alternative to traditional biodiversity assessments, which require high levels of expertise. While eDNA analyses are increasingly being utilized, there remains considerable uncertainty regarding the dynamics of multispecies eDNA, especially in variable systems such as rivers. Here, we utilize four sets of upland stream mesocosms, across an acid–base gradient, to assess the temporal and environmental degradation of multispecies eDNA. Sampling included water column and biofilm sampling over time with eDNA quantified using qPCR. Our findings show that the persistence of lotic multispecies eDNA, sampled from water and biofilm, decays to non-detectable levels within 2 days and that acidic environments accelerate the degradation process. Collectively, the results provide the basis for a predictive framework for the relationship between lotic eDNA degradation dynamics in spatio-temporally dynamic river ecosystems. Nature Publishing Group UK 2018-01-22 /pmc/articles/PMC6123786/ /pubmed/30271891 http://dx.doi.org/10.1038/s42003-017-0005-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Seymour, Mathew
Durance, Isabelle
Cosby, Bernard J.
Ransom-Jones, Emma
Deiner, Kristy
Ormerod, Steve J.
Colbourne, John K.
Wilgar, Gregory
Carvalho, Gary R.
de Bruyn, Mark
Edwards, François
Emmett, Bridget A.
Bik, Holly M.
Creer, Simon
Acidity promotes degradation of multi-species environmental DNA in lotic mesocosms
title Acidity promotes degradation of multi-species environmental DNA in lotic mesocosms
title_full Acidity promotes degradation of multi-species environmental DNA in lotic mesocosms
title_fullStr Acidity promotes degradation of multi-species environmental DNA in lotic mesocosms
title_full_unstemmed Acidity promotes degradation of multi-species environmental DNA in lotic mesocosms
title_short Acidity promotes degradation of multi-species environmental DNA in lotic mesocosms
title_sort acidity promotes degradation of multi-species environmental dna in lotic mesocosms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123786/
https://www.ncbi.nlm.nih.gov/pubmed/30271891
http://dx.doi.org/10.1038/s42003-017-0005-3
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