How much is enough? Examining the sampling effort necessary to estimate mean eDNA concentrations in lentic systems

Author:

Yates M. C.1ORCID,Gaudet‐Boulay M.2,Garcia Machado E.2ORCID,Côté G.3,Gilbert A.4,Bernatchez L.2ORCID

Affiliation:

1. University of Windsor Windsor Ontario Canada

2. Institut de Biologie Intégrative et des Systèmes (IBIS), Pavillon Charles‐Eugène‐Marchand, Université Laval Québec City Québec Canada

3. Ministère de l´Environnement, de la Lutte Contre les Changements Climatiques, de la Faune et des Parcs

4. Société des Établissements de Plein air du Québec (Sépaq) Québec City Québec Canada

Abstract

AbstractThe concentration of eDNA in an environment can provide important ecological information of relevance for management and conservation, but little research has explored optimizing sampling strategies to estimate mean eDNA concentrations in natural environments. Inter‐replicate eDNA concentrations often exhibit right‐skewed “clustered” or “clumped” distributions, likely due to the stochastic capture of large “aggregate” particles with high eDNA copy numbers. This has important potential implications for modeling the resulting sampling effort necessary to accurately quantify eDNA concentrations. In a previous study, 17–20 Brook Charr eDNA samples were collected from 28 lakes in Québec, Canada. We explored how variation in eDNA concentrations within a lake was affected by several habitat characteristics. We then conducted a power analysis to determine the sampling effort (“minimum n”) necessary to accurately quantify mean lake eDNA concentrations and, using simulations, explored how a bimodal distribution of eDNA particle copy count could affect inter‐replicate variability. The median sample size such that 90% of sample mean estimates were within 20% of the “true” mean was 12.5; a sample size of 20 was sufficient to quantify mean concentrations in 21/28 lakes. We found no evidence that temperature or lake size impacted sample variability. We also found that variance among replicates was non‐linearly related to mean lake eDNA concentration across years: variability was lowest at low and high concentrations and highest at intermediate concentrations. We hypothesize that this resulted from the stochastic capture of large “aggregate” particles at intermediate concentrations; at low concentrations, aggregates were likely rarely captured and at high concentrations may represent a consistent component of total eDNA. Simulations demonstrated that these patterns can emerge from some bimodal eDNA particle “size” distributions. Overall, we conclude that sampling efforts in many previous studies (notably including the authors' own) were potentially low, emphasizing the need to increase spatial replication in lentic surveys.

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

Subject

Genetics,Ecology,Ecology, Evolution, Behavior and Systematics

Reference41 articles.

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