Abstract

The exploitation of non-invasive samples has been widely used in genetic monitoring of terrestrial species. In aquatic ecosystems, non-invasive samples such as feces, shed hair or skin, are less accessible. However, the use of environmental DNA (eDNA) has recently been shown to be an effective tool for genetic monitoring of species presence in freshwater ecosystems. Detecting species in the marine environment using eDNA potentially offers a greater challenge due to the greater dilution, amount of mixing and salinity compared with most freshwater ecosystems. To determine the potential use of eDNA for genetic monitoring we used specific primers that amplify short mitochondrial DNA sequences to detect the presence of a marine mammal, the harbor porpoise, Phocoena phocoena, in a controlled environment and in natural marine locations. The reliability of the genetic detections was investigated by comparing with detections of harbor porpoise echolocation clicks by static acoustic monitoring devices. While we were able to consistently genetically detect the target species under controlled conditions, the results from natural locations were less consistent and detection by eDNA was less successful than acoustic detections. However, at one site we detected long-finned pilot whale, Globicephala melas, a species rarely sighted in the Baltic. Therefore, with optimization aimed towards processing larger volumes of seawater this method has the potential to compliment current visual and acoustic methods of species detection of marine mammals.

Highlights

  • The use of molecular genetic markers for monitoring biodiversity and detecting and identifying species, individuals or measuring population genetic parameters can provide valuable information for the management and conservation of species and ecosystems [1]

  • Porpoise DNA was successfully amplified from a pooled sample of the 5 DNA extracts from each of the 15 ml seawater samples collected from the Fjord&Bælt sea pen (Table 1)

  • Assuming optimal polymerase chain reactions (PCRs) efficiency, this suggests a minimal difference of 4–5 orders of magnitude in DNA concentration, as expected for environmental DNA (eDNA) extracts generated from such dilute environmental samples

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Summary

Introduction

The use of molecular genetic markers for monitoring biodiversity and detecting and identifying species, individuals or measuring population genetic parameters can provide valuable information for the management and conservation of species and ecosystems [1]. Non-invasive sampling using hair or scat has been successfully used in genetic monitoring programs of wide-ranging terrestrial or semi-aquatic species, which often occur at low density [1] and can be a lower cost approach than direct sampling as the individual or species does not have to be directly encountered and greater number of samples can be collected. This is offset by what can be increased DNA extraction and sequencing costs and a decrease in returns to the potentially large numbers of duplicate samples [2]. Biological excretory processes such as the sloughing of skin, urination and defecation can be sources of ‘environmental’ DNA (eDNA), and can provide a record of the species’ presence over the period that the DNA persists in the environment [7,8,9,10,11,12,13,14]

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