Environmental DNA reflects spatial distribution of a rare turtle in a lentic wetland assisted colonization site

Author:

Nordstrom Bethany1ORCID,Budd Alyssa2ORCID,Mitchell Nicola1,Cornish Caitlin1,Byrne Margaret13,Kuchling Gerald14,Jarman Simon5

Affiliation:

1. School of Biological Sciences The University of Western Australia Crawley Western Australia Australia

2. Environomics Future Science Platform, Indian Ocean Marine Research Centre Commonwealth Scientific and Industrial Research Organisation (CSIRO) Crawley Western Australia Australia

3. Biodiversity and Conservation Science Department of Biodiversity, Conservation and Attractions Bentley Western Australia Australia

4. Swan Coastal District Department of Biodiversity, Conservation and Attractions Wanneroo Western Australia Australia

5. School of Molecular and Life Sciences Curtin University Bentley, Perth Western Australia Australia

Abstract

AbstractConservation translocations require robust post‐release monitoring to evaluate their success, which can be challenging to implement and maintain. Monitoring techniques that can account for the dispersal and cryptic nature of translocated animals are necessary to provide critical information on persistence and distribution. In this study, we developed a highly sensitive environmental DNA (eDNA) assay specific to the critically endangered western swamp turtle (Pseudemydura umbrina), a species currently undergoing trials of assisted colonization. Actively filtering sufficient volumes of water in lentic systems is difficult due to high concentrations of clogging particulates, therefore we assessed the viability of passive sampling in a controlled environment by submerging filter membranes and directly extracting DNA. Active sampling detected P. umbrina with a 97.6% detection rate, whereas passive sampling resulted in an 8.3% detection rate. We then used a fine‐scale eDNA sampling design and radio‐tracked translocated P. umbrina at the assisted colonization wetland to investigate eDNA dispersal and spatial monitoring resolution. We detected P. umbrina at 42% (7/17) of eDNA sample sites, and the probability of a positive eDNA detection was negatively associated with the distance of P. umbrina from the sampling site, indicating limited eDNA dispersal from the source. Systems with low natural mixing and limited eDNA dispersal provide an opportunity for high‐resolution spatial and temporal monitoring via targeted eDNA approaches. This is beneficial for monitoring rare species in these systems, as such high‐resolution results can provide insights into species presence, distribution, and microhabitat use.

Funder

Holsworth Wildlife Research Endowment

Publisher

Wiley

Subject

Genetics,Ecology,Ecology, Evolution, Behavior and Systematics

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