Improved biodiversity detection using a large-volume environmental DNA sampler with in situ filtration and implications for marine eDNA sampling strategies

dc.contributor.author Govindarajan, Annette F.
dc.contributor.author McCartin, Luke
dc.contributor.author Adams, Allan
dc.contributor.author Allan, Elizabeth
dc.contributor.author Belani, Abhimanyu
dc.contributor.author Francolini, Rene
dc.contributor.author Fujii, Justin
dc.contributor.author Gomez-Ibañez, Daniel
dc.contributor.author Kukulya, Amy
dc.contributor.author Marin, Fredrick
dc.contributor.author Tradd, Kaitlyn
dc.contributor.author Yoerger, Dana R.
dc.contributor.author McDermott, Jill M.
dc.contributor.author Herrera, Santiago
dc.date.accessioned 2023-03-22T18:12:25Z
dc.date.available 2023-03-22T18:12:25Z
dc.date.issued 2022-09-22
dc.description © The Author(s), 2022. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Govindarajan, A., McCartin, L., Adams, A., Allan, E., Belani, A., Francolini, R., Fujii, J., Gomez-Ibañez, D., Kukulya, A., Marin, F., Tradd, K., Yoerger, D., McDermott, J., & Herrera, S. Improved biodiversity detection using a large-volume environmental DNA sampler with in situ filtration and implications for marine eDNA sampling strategies. Deep Sea Research Part I: Oceanographic Research Papers, 189, (2022): 103871, https://doi.org/10.1016/j.dsr.2022.103871.
dc.description.abstract Metabarcoding analysis of environmental DNA samples is a promising new tool for marine biodiversity and conservation. Typically, seawater samples are obtained using Niskin bottles and filtered to collect eDNA. However, standard sample volumes are small relative to the scale of the environment, conventional collection strategies are limited, and the filtration process is time consuming. To overcome these limitations, we developed a new large – volume eDNA sampler with in situ filtration, capable of taking up to 12 samples per deployment. We conducted three deployments of our sampler on the robotic vehicle Mesobot in the Flower Garden Banks National Marine Sanctuary in the northwestern Gulf of Mexico and collected samples from 20 to 400 m depth. We compared the large volume (∼40–60 L) samples collected by Mesobot with small volume (∼2 L) samples collected using the conventional CTD rosette – mounted Niskin bottle approach. We sequenced the V9 region of 18S rRNA, which detects a broad range of invertebrate taxa, and found that while both methods detected biodiversity changes associated with depth, our large volume samples detected approximately 66% more taxa than the CTD small volume samples. We found that the fraction of the eDNA signal originating from metazoans relative to the total eDNA signal decreased with sampling depth, indicating that larger volume samples may be especially important for detecting metazoans in mesopelagic and deep ocean environments. We also noted substantial variability in biological replicates from both the large volume Mesobot and small volume CTD sample sets. Both of the sample sets also identified taxa that the other did not – although the number of unique taxa associated with the Mesobot samples was almost four times larger than those from the CTD samples. Large volume eDNA sampling with in situ filtration, particularly when coupled with robotic platforms, has great potential for marine biodiversity surveys, and we discuss practical methodological and sampling considerations for future applications.•A large-volume eDNA sampler was developed and deployed on the midwater robot Mesobot.•Compared to conventional small-volume samples, the sampler detected more metazoan taxa.•Both sampling approaches detected community changes with depth on the scale of 10's of meters.•The metazoan eDNA signal declined with depth.•Large volume sampling may be especially important in the mesopelagic and deep sea.
dc.description.sponsorship This research is part of the Woods Hole Oceanographic Institution's Ocean Twilight Zone Project, funded as part of The Audacious Project housed at TED, and a result of research funded by the National Oceanic and Atmospheric Administration's Oceanic and Atmospheric Research, Office of Ocean Exploration and Research, under award NA18OAR0110289 to Lehigh University (SH and JM co-PIs). The work of AA was supported in part by the Future Oceans Lab Acceleration Fund. The work on the sampler pumps was supported by funding from UNH Subaward No. 19–015 on NOAA Federal Award No. NA17NOS0080203 to AK.
dc.identifier.citation Govindarajan, A., McCartin, L., Adams, A., Allan, E., Belani, A., Francolini, R., Fujii, J., Gomez-Ibañez, D., Kukulya, A., Marin, F., Tradd, K., Yoerger, D., McDermott, J., & Herrera, S. (2022). Improved biodiversity detection using a large-volume environmental DNA sampler with in situ filtration and implications for marine eDNA sampling strategies. Deep Sea Research Part I: Oceanographic Research Papers, 189, 103871.
dc.identifier.doi 10.1016/j.dsr.2022.103871
dc.identifier.uri https://hdl.handle.net/1912/65817
dc.publisher Elsevier
dc.relation.uri https://doi.org/10.1016/j.dsr.2022.103871
dc.rights Attribution 4.0 International
dc.rights.uri http://creativecommons.org/licenses/by/4.0/
dc.subject Environmental DNA
dc.subject Metabarcoding
dc.subject Biodiversity
dc.subject Autonomous sampling
dc.subject Mesopelagic
dc.subject Gulf of Mexico
dc.title Improved biodiversity detection using a large-volume environmental DNA sampler with in situ filtration and implications for marine eDNA sampling strategies
dc.type Article
dspace.entity.type Publication
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