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Related Concept Videos

Sampling Methods: Sample Types01:18

Sampling Methods: Sample Types

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Sampling materials are classified into three main types: solid, liquid, and gas.
Solid samples include a variety of substances, such as sediments from water bodies, soil, metals, and biological tissues. Two standard methods for extracting sediments from water bodies are grab sampling and piston coring. Grab sampling involves using a device to collect a discrete sediment sample from the bottom of a water body with minimal disturbance. Grab samples do not always represent the entire area due to...
214

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Use of a Filter Cartridge for Filtration of Water Samples and Extraction of Environmental DNA
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Using low volume eDNA methods to sample pelagic marine animal assemblages.

Michelle E Dan1, Elan J Portner1, Jeff S Bowman1

  • 1Integrative Oceanography Division, Scripps Institution of Oceanography, University of California San Diego, La Jolla, California, United States of America.

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Environmental DNA (eDNA) analysis of low-volume water samples effectively detects diverse marine life, including deep-sea species. This method offers higher biodiversity detection than traditional trawls, especially as reference libraries expand.

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Area of Science:

  • Marine Biology
  • Molecular Ecology
  • Environmental Science

Background:

  • Environmental DNA (eDNA) is a powerful tool for marine biodiversity assessment.
  • Traditional sampling methods often require large water volumes, posing challenges for ship-based programs.
  • Limited research exists on eDNA performance in low-volume deep-sea samples.

Purpose of the Study:

  • To evaluate the efficacy of low-volume eDNA sampling for detecting pelagic marine animals.
  • To compare eDNA diversity with traditional pelagic trawl samples in the California Current.
  • To assess the impact of sampling depth on eDNA detection and taxonomic resolution.

Main Methods:

  • Analysis of 436 low-volume (380-1800 mL) eDNA seawater samples from 0-2200 m depth.
  • Utilized 12S rRNA and COI gene primers to quantify micronekton, fishes, and zooplankton.
  • Compared eDNA results with 27 concurrent pelagic trawl samples.

Main Results:

  • eDNA samples detected higher vertebrate and invertebrate diversity than trawl samples.
  • Assemblage composition differences were linked to size-selectivity and primer suitability.
  • Species-level identification of invertebrates decreased with sampling depth.
  • No significant variation in reads or ASVs between shallow and deep samples.

Conclusions:

  • Low-volume eDNA sampling is effective for quantifying marine animal assemblages, including deep-sea species.
  • eDNA offers broader taxonomic detection compared to traditional trawling methods.
  • Expanding reference libraries will enhance eDNA's utility for deep-sea invertebrate identification.