Preliminary evaluation of the performance of eDNA for marine species detection

Environmental DNA (eDNA) is the collective term for DNA molecules that are released from living or dead organisms in the form of blood, skin, mucous, gametes or faeces into the environment. Subsequently eDNA can be extracted from environmental samples such as water, air or. Techniques employing eDNA...

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Main Authors: Jens Carlson, Jeanette Carlsson
Format: Conference Object
Language:unknown
Published: 2017
Subjects:
Online Access:https://zenodo.org/record/571062
https://doi.org/10.5281/zenodo.571062
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spelling ftzenodo:oai:zenodo.org:571062 2023-05-15T17:08:48+02:00 Preliminary evaluation of the performance of eDNA for marine species detection Jens Carlson Jeanette Carlsson 2017-04-25 https://zenodo.org/record/571062 https://doi.org/10.5281/zenodo.571062 unknown info:eu-repo/grantAgreement/EC/H2020/678760/ https://zenodo.org/communities/atlas https://zenodo.org/record/571062 https://doi.org/10.5281/zenodo.571062 oai:zenodo.org:571062 info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by/4.0/legalcode info:eu-repo/semantics/lecture presentation 2017 ftzenodo https://doi.org/10.5281/zenodo.571062 2023-03-10T22:35:58Z Environmental DNA (eDNA) is the collective term for DNA molecules that are released from living or dead organisms in the form of blood, skin, mucous, gametes or faeces into the environment. Subsequently eDNA can be extracted from environmental samples such as water, air or. Techniques employing eDNA are non-invasive (i.e. do not require the direct observation or sampling of an organism), instead relying on DNA found in the environment as a source of information. As a result, eDNA is rapidly emerging as a valuable tool for assessing species presence and biodiversity monitoring. There are two methods for analysing eDNA – metabarcoding and quantitative (q)PCR. Both methods are usually targeting mitochondrial (mt)DNA due to the much higher copy number per cell than nuclear (n)DNA. While metabarcoding detects multiple species, qPCR is species (or taxanomical group specific). Specific probes and primers bind to target sequences (i.e. specific species) in the eDNA sample. An advantage of qPCR over metabarcoding is that only targets species specific DNA and not, as metabarcoding, multiple species making qPCR more sensitive and can detect lower concentrations of eDNA. In addition, it has been used to estimate the relative biomass of the target. However, qPCR cannot detect biodiversity as the method will only target what is being searched for while metabarcoding can target a wide range of taxa simultaneously. The purpose is to develop and validate species-specific qPCR assays for eDNA and deploy these approaches in ATLAS areas. The sampling will consists of water samples from different depths. Water samples will be filtered and filters preserved until analysed. These objectives are divided into tasks as follows: (i) cold-water coral Lophelia pertusa, (ii) vulnerable deep-sea seamount fish species Hoplostethus atlanticus or Beryx decadactylus, (iii) assess qPCR as a tool for estimating biomass of deep-sea fish species Helicolenus dactylopterus, (iv) qPCR analyses to help identifying seamount hotspots of pelagic ... Conference Object Lophelia pertusa Zenodo
institution Open Polar
collection Zenodo
op_collection_id ftzenodo
language unknown
description Environmental DNA (eDNA) is the collective term for DNA molecules that are released from living or dead organisms in the form of blood, skin, mucous, gametes or faeces into the environment. Subsequently eDNA can be extracted from environmental samples such as water, air or. Techniques employing eDNA are non-invasive (i.e. do not require the direct observation or sampling of an organism), instead relying on DNA found in the environment as a source of information. As a result, eDNA is rapidly emerging as a valuable tool for assessing species presence and biodiversity monitoring. There are two methods for analysing eDNA – metabarcoding and quantitative (q)PCR. Both methods are usually targeting mitochondrial (mt)DNA due to the much higher copy number per cell than nuclear (n)DNA. While metabarcoding detects multiple species, qPCR is species (or taxanomical group specific). Specific probes and primers bind to target sequences (i.e. specific species) in the eDNA sample. An advantage of qPCR over metabarcoding is that only targets species specific DNA and not, as metabarcoding, multiple species making qPCR more sensitive and can detect lower concentrations of eDNA. In addition, it has been used to estimate the relative biomass of the target. However, qPCR cannot detect biodiversity as the method will only target what is being searched for while metabarcoding can target a wide range of taxa simultaneously. The purpose is to develop and validate species-specific qPCR assays for eDNA and deploy these approaches in ATLAS areas. The sampling will consists of water samples from different depths. Water samples will be filtered and filters preserved until analysed. These objectives are divided into tasks as follows: (i) cold-water coral Lophelia pertusa, (ii) vulnerable deep-sea seamount fish species Hoplostethus atlanticus or Beryx decadactylus, (iii) assess qPCR as a tool for estimating biomass of deep-sea fish species Helicolenus dactylopterus, (iv) qPCR analyses to help identifying seamount hotspots of pelagic ...
format Conference Object
author Jens Carlson
Jeanette Carlsson
spellingShingle Jens Carlson
Jeanette Carlsson
Preliminary evaluation of the performance of eDNA for marine species detection
author_facet Jens Carlson
Jeanette Carlsson
author_sort Jens Carlson
title Preliminary evaluation of the performance of eDNA for marine species detection
title_short Preliminary evaluation of the performance of eDNA for marine species detection
title_full Preliminary evaluation of the performance of eDNA for marine species detection
title_fullStr Preliminary evaluation of the performance of eDNA for marine species detection
title_full_unstemmed Preliminary evaluation of the performance of eDNA for marine species detection
title_sort preliminary evaluation of the performance of edna for marine species detection
publishDate 2017
url https://zenodo.org/record/571062
https://doi.org/10.5281/zenodo.571062
genre Lophelia pertusa
genre_facet Lophelia pertusa
op_relation info:eu-repo/grantAgreement/EC/H2020/678760/
https://zenodo.org/communities/atlas
https://zenodo.org/record/571062
https://doi.org/10.5281/zenodo.571062
oai:zenodo.org:571062
op_rights info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by/4.0/legalcode
op_doi https://doi.org/10.5281/zenodo.571062
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