Abstract

AbstractEarly life stage (ELS) fishes provide a valuable metric for species, population, and ecosystem monitoring. Industrial, manufacturing, and power generating facilities in the United States can be required to monitor ELS fishes to assess impacts of facility intake waters. Traditional methods for collecting, identifying, and enumerating ELS fishes include ichthyoplankton netting and pumping from intake and discharge waters. However, sampling at these sites can prove challenging from logistical and safety standpoints, with added challenges of identifying and post‐processing of ELS fishes to quantify facility impacts on waterbodies for regulatory purposes. Methods utilizing environmental DNA (eDNA) may offer improvements in these areas. This study assessed the utility of novel, species‐specific qPCR assays to detect eDNA from three differentially abundant fish species (alewife (Alosa pseudoharengus; Wilson, 1811), gizzard shad (Dorosoma cepedianum; Lesueur, 1818), and yellow perch (Perca flavescens; Mitchill, 1814)) at the outflow of an industrial site. eDNA concentrations were compared with abundance estimates derived from two conventional collection methods to explore the potential utility of eDNA‐based methods in future monitoring. The likelihood of detecting gizzard shad, yellow perch, and alewife in the discharge waters of the power generation station was not significantly different among eDNA, plankton netting, or pump sampling. Results suggest successful detections differ by species and time of year for each method. Gizzard shad eDNA relative abundance correlated strongly with total larval abundances captured by the pumping but not the netting methods, whereas yellow perch eDNA abundance was found to correlate with both conventional methods. Alewife was not detected by any method, consistent with documentation of the decline in this species within the lake. Overall, our study found a positive relationship between eDNA abundance and larval fish abundance in both daily and seasonal sampling, suggesting that fluctuations in eDNA concentration may be linked to larval abundance.

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