4.7 Article

Environmental DNA metabarcoding as a tool for biodiversity assessment and monitoring: reconstructing established fish communities of north-temperate lakes and rivers

Journal

DIVERSITY AND DISTRIBUTIONS
Volume 27, Issue 10, Pages 1966-1980

Publisher

WILEY
DOI: 10.1111/ddi.13253

Keywords

12S; community ecology; eDNA; fisheries; metagenomics; upper Mississippi River; Wisconsin lakes

Funding

  1. U.S. Geological Survey Invasive Species Program
  2. Research Computing Clusters at Old Dominion University

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Using precipitation-based environmental DNA sample collection and mitochondrial 12S metabarcoding sequencing can reconstruct well-studied fish communities in lakes and rivers. eDNA species detections correlate with known community composition, and the efficiency of eDNA detection of fish biodiversity varies among different systems.
Aim To evaluate the ability of precipitation-based environmental DNA (eDNA) sample collection and mitochondrial 12S metabarcoding sequencing to reconstruct well-studied fish communities in lakes and rivers. Specific objectives were to 1) determine correlations between eDNA species detections and known community composition based on conventional field sampling, 2) compare efficiency of eDNA to detect fish biodiversity among systems with variable morphologies and trophic states, and 3) determine if species habitat preferences predict eDNA detection. Location Upper Great Lakes Region, North America. Methods Fish community composition was estimated for seven lakes and two Mississippi River navigation pools using sequence data from the mitochondrial 12S gene amplified from 10 to 50 water samples per waterbody collected in 50-mL centrifuge tubes at a single time point. Environmental DNA (eDNA) was concentrated without filtration by centrifuging samples to reduce per-sample handling time. Taxonomic detections from eDNA were compared to established community monitoring databases containing up to 40 years of sampling and a detailed habitat/substrate preference matrix to identify patterns of bias. Results Mitochondrial 12S gene metabarcoding detected 15%-47% of the known species at each waterbody and 30%-76% of known genera. Non-metric multidimensional scaling (NMDS) assessment of the community structure indicated that eDNA-detected communities grouped in a similar pattern as known communities. Discriminant analysis of principal components indicated that there was a high degree of overlap in habitat/substrate preference of eDNA-detected and eDNA-undetected species suggesting limited habitat bias for eDNA sampling. Main conclusions Large numbers of small volume samples sequenced at the mitochondrial 12S gene can describe the coarse community structure of freshwater systems. However, additional conventional sampling and environmental DNA sampling may be necessary for a complete diversity census.

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