Data from: Residual eDNA detection sensitivity assessed by quantitative real-time PCR in a river ecosystem ...

Several studies have demonstrated that environmental DNA (eDNA) can be used to detect the presence of aquatic species, days to weeks after the target species has been removed. However, most studies used eDNA analysis in lentic systems (ponds or lakes), or in controlled laboratory experiments. While...

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Main Authors: Balasingham, Katherine D., Walter, Ryan P., Heath, Daniel D.
Format: Dataset
Language:English
Published: Dryad 2016
Subjects:
Online Access:https://dx.doi.org/10.5061/dryad.5rf92
https://datadryad.org/stash/dataset/doi:10.5061/dryad.5rf92
id ftdatacite:10.5061/dryad.5rf92
record_format openpolar
spelling ftdatacite:10.5061/dryad.5rf92 2024-02-04T10:04:16+01:00 Data from: Residual eDNA detection sensitivity assessed by quantitative real-time PCR in a river ecosystem ... Balasingham, Katherine D. Walter, Ryan P. Heath, Daniel D. 2016 https://dx.doi.org/10.5061/dryad.5rf92 https://datadryad.org/stash/dataset/doi:10.5061/dryad.5rf92 en eng Dryad https://dx.doi.org/10.1111/1755-0998.12598 Creative Commons Zero v1.0 Universal https://creativecommons.org/publicdomain/zero/1.0/legalcode cc0-1.0 qRT-PCR Residual DNA persistence Dataset dataset 2016 ftdatacite https://doi.org/10.5061/dryad.5rf9210.1111/1755-0998.12598 2024-01-05T01:14:15Z Several studies have demonstrated that environmental DNA (eDNA) can be used to detect the presence of aquatic species, days to weeks after the target species has been removed. However, most studies used eDNA analysis in lentic systems (ponds or lakes), or in controlled laboratory experiments. While eDNA degrades rapidly in all aquatic systems, it also undergoes dilution effects and physical destruction in flowing systems, complicating detection in rivers. However, some eDNA (i.e. residual eDNA) can be retained in aquatic systems, even those subject to high flow regimes. Our goal was to determine residual eDNA detection sensitivity using quantitative real-time polymerase chain reaction (qRT-PCR), in a flowing, uncontrolled river after the eDNA source was removed from the system; we repeated the experiment over two years. Residual eDNA had the strongest signal strength at the original source site and was detectable there up to 11.5 hours after eDNA source removal. Residual eDNA signal strength decreased as ... : Appendix S1. Ct values for qRT-PCR efficiency for Salmo salar.Ct values for Figure 2. 10-fold Salmo salar dilution series with Salmo_Mito-951 (d-loop; Karlsson et al. 2012) primer set.Suppl Info - Appendix S1. Ct values for qRT-PCR efficiency.xlsxAppendix S2. Little River 2014 qRT-PCR Ct values.Ct values for Figure 3A. Little River 2014 river samples. Primer set Salmo_Mito-951 (Karlsson et al. 2012).Suppl Info - Appendix S2. Little River 2014 qRT-PCR Ct values.xlsxAppendix S3. Little River 2015 qRT-PCR Ct values.Ct values for Figure 3B. Little River 2015 samples. Primer set Salmo_Mito-951 (Karlsson et al. 2012).Suppl Info - Appendix S3. Little River 2015 qRT-PCR Ct values.xlsx ... Dataset Salmo salar DataCite Metadata Store (German National Library of Science and Technology) Little River ENVELOPE(-135.687,-135.687,60.894,60.894)
institution Open Polar
collection DataCite Metadata Store (German National Library of Science and Technology)
op_collection_id ftdatacite
language English
topic qRT-PCR
Residual
DNA persistence
spellingShingle qRT-PCR
Residual
DNA persistence
Balasingham, Katherine D.
Walter, Ryan P.
Heath, Daniel D.
Data from: Residual eDNA detection sensitivity assessed by quantitative real-time PCR in a river ecosystem ...
topic_facet qRT-PCR
Residual
DNA persistence
description Several studies have demonstrated that environmental DNA (eDNA) can be used to detect the presence of aquatic species, days to weeks after the target species has been removed. However, most studies used eDNA analysis in lentic systems (ponds or lakes), or in controlled laboratory experiments. While eDNA degrades rapidly in all aquatic systems, it also undergoes dilution effects and physical destruction in flowing systems, complicating detection in rivers. However, some eDNA (i.e. residual eDNA) can be retained in aquatic systems, even those subject to high flow regimes. Our goal was to determine residual eDNA detection sensitivity using quantitative real-time polymerase chain reaction (qRT-PCR), in a flowing, uncontrolled river after the eDNA source was removed from the system; we repeated the experiment over two years. Residual eDNA had the strongest signal strength at the original source site and was detectable there up to 11.5 hours after eDNA source removal. Residual eDNA signal strength decreased as ... : Appendix S1. Ct values for qRT-PCR efficiency for Salmo salar.Ct values for Figure 2. 10-fold Salmo salar dilution series with Salmo_Mito-951 (d-loop; Karlsson et al. 2012) primer set.Suppl Info - Appendix S1. Ct values for qRT-PCR efficiency.xlsxAppendix S2. Little River 2014 qRT-PCR Ct values.Ct values for Figure 3A. Little River 2014 river samples. Primer set Salmo_Mito-951 (Karlsson et al. 2012).Suppl Info - Appendix S2. Little River 2014 qRT-PCR Ct values.xlsxAppendix S3. Little River 2015 qRT-PCR Ct values.Ct values for Figure 3B. Little River 2015 samples. Primer set Salmo_Mito-951 (Karlsson et al. 2012).Suppl Info - Appendix S3. Little River 2015 qRT-PCR Ct values.xlsx ...
format Dataset
author Balasingham, Katherine D.
Walter, Ryan P.
Heath, Daniel D.
author_facet Balasingham, Katherine D.
Walter, Ryan P.
Heath, Daniel D.
author_sort Balasingham, Katherine D.
title Data from: Residual eDNA detection sensitivity assessed by quantitative real-time PCR in a river ecosystem ...
title_short Data from: Residual eDNA detection sensitivity assessed by quantitative real-time PCR in a river ecosystem ...
title_full Data from: Residual eDNA detection sensitivity assessed by quantitative real-time PCR in a river ecosystem ...
title_fullStr Data from: Residual eDNA detection sensitivity assessed by quantitative real-time PCR in a river ecosystem ...
title_full_unstemmed Data from: Residual eDNA detection sensitivity assessed by quantitative real-time PCR in a river ecosystem ...
title_sort data from: residual edna detection sensitivity assessed by quantitative real-time pcr in a river ecosystem ...
publisher Dryad
publishDate 2016
url https://dx.doi.org/10.5061/dryad.5rf92
https://datadryad.org/stash/dataset/doi:10.5061/dryad.5rf92
long_lat ENVELOPE(-135.687,-135.687,60.894,60.894)
geographic Little River
geographic_facet Little River
genre Salmo salar
genre_facet Salmo salar
op_relation https://dx.doi.org/10.1111/1755-0998.12598
op_rights Creative Commons Zero v1.0 Universal
https://creativecommons.org/publicdomain/zero/1.0/legalcode
cc0-1.0
op_doi https://doi.org/10.5061/dryad.5rf9210.1111/1755-0998.12598
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