COS 63-7 - A detection protocol that increases the sensitivity of environmental DNA (eDNA) monitoring for aquatic organisms

Tuesday, August 8, 2017: 3:40 PM
E147-148, Oregon Convention Center

ABSTRACT WITHDRAWN

Breanna R. Caton, University of Toledo; William V. Sigler, University of Toledo; Carol A. Stepien, University of Toledo; John W. Turner Jr., University of Toledo; Daryl L. Moorhead, University of Toledo; Daryl F. Dwyer, University of Toledo

Background/Question/Methods

The emerging molecular techniques of environmental DNA (eDNA) offer the potential to detect the species composition of an ecosystem by means of non-invasive environmental (water) sampling. Despite the radiation of eDNA research since 2008, there are still large knowledge gaps and a need for standardized methods that must be addressed before eDNA can be utilized as a wide-spread management tool. Employing the round goby (Neogobius melanostomus) as a model organism, species-specific cytochrome b primers were developed for a series of laboratory and field experiments to evaluate eDNA detection efficacy under local environmental conditions.

Results/Conclusions

The benefits of this qPCR testing protocol are: results that accurately determine environmental residence time; generation of gene sequences suitable for population genetic analysis; and decreased likelihood of false positive results from cross-amplification. This eDNA protocol is optimized for higher resolution species-specific surveys for aquatic organisms requiring time-sensitive monitoring. Potential management applications include: invasive species surveillance, evaluation of eradication efforts, monitoring the movement of populations, and environmental impact assessment surveys.