Abstract

Environmental DNA (eDNA) analysis of water samples is on the brink of becoming a standard monitoring method for aquatic species. This method has improved detection rates over conventional survey methods and thus has demonstrated effectiveness for estimation of site occupancy and species distribution. The frontier of eDNA applications, however, is to infer species density. Building upon previous studies, we present and assess a modeling approach that aims at inferring animal density from eDNA. The modeling combines eDNA and animal count data from a subset of sites to estimate species density (and associated uncertainties) at other sites where only eDNA data are available. As a proof of concept, we first perform a cross‐validation study using experimental data on carp in mesocosms. In these data, fish densities are known without error, which allows us to test the performance of the method with known data. We then evaluate the model using field data from a study on a stream salamander species to assess the potential of this method to work in natural settings, where density can never be known with absolute certainty. Two alternative distributions (Normal and Negative Binomial) to model variability in eDNA concentration data are assessed. Assessment based on the proof of concept data (carp) revealed that the Negative Binomial model provided much more accurate estimates than the model based on a Normal distribution, likely because eDNA data tend to be overdispersed. Greater imprecision was found when we applied the method to the field data, but the Negative Binomial model still provided useful density estimates. We call for further model development in this direction, as well as further research targeted at sampling design optimization. It will be important to assess these approaches on a broad range of study systems.

Highlights

  • Assessing status and trends of wild populations and communities is a challenging endeavor, especially for species that are difficult to detect (Williams, Nichols, & Conroy, 2002)

  • (β) describing the relationship f() between animal density Di and the expected value of the environmental DNA (eDNA) metric E(wik) (in the models discussed below we model this as a simple linear relationship, as E(wik) = β0 × Di, where parameter β0 is the coefficient characterizing the relationship between animal density (Di) and the expected concentration of eDNA E(wik)); (2) parameter(s) (θ) that are specific to the probabilistic distribution chosen and describe variability of the realized eDNA data wik around the theoretic expected value E(wik); and (3) the unknown values of animal density (Di) for any site i ≠ j

  • Before running analyses with our new modeling approach, we looked at correlations between values of eDNA concentration and animal density, to get a sense of the “quality” of information contained in the dataset

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Summary

| INTRODUCTION

Assessing status and trends of wild populations and communities is a challenging endeavor, especially for species that are difficult to detect (Williams, Nichols, & Conroy, 2002). For diffusion-­limited lentic waters where eDNA concentrations are likely to reflect space use of the target species (e.g., Eichmiller et al, 2014), the sampling unit should be carefully identified and sampling replicates collected identically over the area of inference. Such a “snapshot” sampling design is probably more reliable than using temporally separated replicates, given that temporal variability in environmental conditions can affect eDNA. Our results (below) suggest that very few dual data sites (e.g., J = 3–5) are necessary for the model to work properly and provide accurate estimates when the relationship between eDNA concentration and animal density is constant across sampled sites (i.e., over space and time). EDNA values must first be transformed as integers, like we did in our salamander example

| Material and methods
| Results
| DISCUSSION
DATA ACCESSIBILITY
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