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      Water, water everywhere: environmental DNA can unlock population structure in elusive marine species

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          Abstract

          Determining management units for natural populations is critical for effective conservation and management. However, collecting the requisite tissue samples for population genetic analyses remains the primary limiting factor for a number of marine species. The harbour porpoise ( Phocoena phocoena), one of the smallest cetaceans in the Northern Hemisphere, is a primary example. These elusive, highly mobile small animals confound traditional approaches of collecting tissue samples for genetic analyses, yet their nearshore habitat makes them highly vulnerable to fisheries by-catch and the effects of habitat degradation. By exploiting the naturally shed cellular material in seawater and the power of next-generation sequencing, we develop a novel approach for generating population-specific mitochondrial sequence data from environmental DNA (eDNA) using surface seawater samples. Indications of significant genetic differentiation within a currently recognized management stock highlights the need for dedicated eDNA sampling throughout the population's range in southeast Alaska. This indirect sampling tactic for characterizing stock structure of small and endangered marine mammals has the potential to revolutionize population assessment for otherwise inaccessible marine taxa.

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          Most cited references36

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          Next-generation monitoring of aquatic biodiversity using environmental DNA metabarcoding.

          Global biodiversity in freshwater and the oceans is declining at high rates. Reliable tools for assessing and monitoring aquatic biodiversity, especially for rare and secretive species, are important for efficient and timely management. Recent advances in DNA sequencing have provided a new tool for species detection from DNA present in the environment. In this study, we tested whether an environmental DNA (eDNA) metabarcoding approach, using water samples, can be used for addressing significant questions in ecology and conservation. Two key aquatic vertebrate groups were targeted: amphibians and bony fish. The reliability of this method was cautiously validated in silico, in vitro and in situ. When compared with traditional surveys or historical data, eDNA metabarcoding showed a much better detection probability overall. For amphibians, the detection probability with eDNA metabarcoding was 0.97 (CI = 0.90-0.99) vs. 0.58 (CI = 0.50-0.63) for traditional surveys. For fish, in 89% of the studied sites, the number of taxa detected using the eDNA metabarcoding approach was higher or identical to the number detected using traditional methods. We argue that the proposed DNA-based approach has the potential to become the next-generation tool for ecological studies and standardized biodiversity monitoring in a wide range of aquatic ecosystems.
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            Quantifying effects of UV-B, temperature, and pH on eDNA degradation in aquatic microcosms

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              DNA barcoding and metabarcoding of standardized samples reveal patterns of marine benthic diversity.

              Documenting the diversity of marine life is challenging because many species are cryptic, small, and rare, and belong to poorly known groups. New sequencing technologies, especially when combined with standardized sampling, promise to make comprehensive biodiversity assessments and monitoring feasible on a large scale. We used this approach to characterize patterns of diversity on oyster reefs across a range of geographic scales comprising a temperate location [Virginia (VA)] and a subtropical location [Florida (FL)]. Eukaryotic organisms that colonized multilayered settlement surfaces (autonomous reef monitoring structures) over a 6-mo period were identified by cytochrome c oxidase subunit I barcoding (>2-mm mobile organisms) and metabarcoding (sessile and smaller mobile organisms). In a total area of ∼ 15.64 m(2) and volume of ∼ 0.09 m(3), 2,179 operational taxonomic units (OTUs) were recorded from 983,056 sequences. However, only 10.9% could be matched to reference barcodes in public databases, with only 8.2% matching barcodes with both genus and species names. Taxonomic coverage was broad, particularly for animals (22 phyla recorded), but 35.6% of OTUs detected via metabarcoding could not be confidently assigned to a taxonomic group. The smallest size fraction (500 to 106 μm) was the most diverse (more than two-thirds of OTUs). There was little taxonomic overlap between VA and FL, and samples separated by ∼ 2 m were significantly more similar than samples separated by ∼ 100 m. Ground-truthing with independent assessments of taxonomic composition indicated that both presence-absence information and relative abundance information are captured by metabarcoding data, suggesting considerable potential for ecological studies and environmental monitoring.
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                Author and article information

                Journal
                R Soc Open Sci
                R Soc Open Sci
                RSOS
                royopensci
                Royal Society Open Science
                The Royal Society Publishing
                2054-5703
                August 2018
                8 August 2018
                8 August 2018
                : 5
                : 8
                : 180537
                Affiliations
                [1 ]Under Contract to NOAA, National Marine Fisheries Service, Marine Mammal Laboratory, Alaska Fisheries Science Center , 7600 Sand Point Way NE, Seattle, WA 98115, USA
                [2 ]Marine Mammal Laboratory, Alaska Fisheries Science Center , 7600 Sand Point Way NE, Seattle, WA 98115, USA
                [3 ]Under Contract to NOAA, National Marine Fisheries Service , 2725 Montlake Boulevard E, Seattle, WA 98112, USA
                [4 ]Northwest Fisheries Science Center , 2725 Montlake Boulevard E, Seattle, WA 98112, USA
                Author notes
                Author for correspondence: Kim M. Parsons e-mail: kim.parsons@ 123456noaa.gov

                Electronic supplementary material is available online at https://doi.org/10.6084/m9.figshare.c.4171187.

                Author information
                http://orcid.org/0000-0003-4580-3651
                Article
                rsos180537
                10.1098/rsos.180537
                6124077
                30225045
                d64df118-a79d-42c8-b478-8fbaf5f75be7
                © 2018 The Authors.

                Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.

                History
                : 4 April 2018
                : 6 July 2018
                Funding
                Funded by: NOAA Office of Protected Resources;
                Funded by: NOAA Fisheries, NMFS;
                Categories
                1001
                60
                197
                Genetics and Genomics
                Research Article
                Custom metadata
                August, 2018

                porpoise,environmental dna,population genetics,cetacean,stock,next-generation sequencing

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