Including environmental covariates clarifies the relationship between endangered Atlantic salmon ( Salmo salar ) abundance and environmental <scp>DNA</scp>

Abstract Collecting environmental DNA (eDNA) as a nonlethal sampling approach has been valuable in detecting the presence/absence of many imperiled taxa; however, its application to indicate species abundance poses many challenges. A deeper understanding of eDNA dynamics in aquatic systems is requir...

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Bibliographic Details
Published in:Environmental DNA
Main Authors: Morrison, Melissa K., Lacoursière‐Roussel, Anaïs, Wood, Zachary T., Trudel, Marc, Gagné, Nellie, LeBlanc, Francis, Samways, Kurt, Kinnison, Michael T., Pavey, Scott A.
Other Authors: Canada Foundation for Innovation, Canada Research Chairs, Fisheries and Oceans Canada, Natural Sciences and Engineering Research Council of Canada, New Brunswick Innovation Foundation
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2023
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Online Access:http://dx.doi.org/10.1002/edn3.424
https://onlinelibrary.wiley.com/doi/pdf/10.1002/edn3.424
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Summary:Abstract Collecting environmental DNA (eDNA) as a nonlethal sampling approach has been valuable in detecting the presence/absence of many imperiled taxa; however, its application to indicate species abundance poses many challenges. A deeper understanding of eDNA dynamics in aquatic systems is required to better interpret the substantial variability often associated with eDNA samples. Our sampling design took advantage of natural variation in juvenile Atlantic salmon ( Salmo salar ) distribution and abundance along 9 km of a single river in the Province of New Brunswick (Canada), covering different spatial and temporal scales to address the unknown seasonal impacts of environmental variables on the quantitative relationship between eDNA concentration and species abundance. First, we asked whether accounting for environmental variables strengthened the relationship between eDNA and salmon abundance by sampling eDNA during their spring seaward migration. Second, we asked how environmental variables affected eDNA dynamics during the summer as the parr abundance remained relatively constant. Spring eDNA samples were collected over a 6‐week period (12 times) near a rotary screw trap that captured approximately 18.6% of migrating smolts, whereas summer sampling occurred (i) at three distinct salmon habitats (9 times) and (ii) along the full 9 km (3 times). We modeled eDNA concentration as a product of fish abundance and environmental variables, demonstrating that (1) with inclusion of abundance and environmental covariates, eDNA was highly correlated with spring smolt abundance and (2) the relationships among environmental covariates and eDNA were affected by seasonal variation with relatively constant parr abundance in summer. Our findings underscore that with appropriate study design that accounts for seasonal environmental variation and life history phenology, eDNA salmon population assessments may have the potential to evaluate abundance fluctuations in spring and summer.