Journal Article
Rapid detection of subterranean fauna from passive sampling of groundwater eDNA
van der Heyde, M., Alexander, J., Nevill, P., Austin, A.D., Stevens, N., Jones, M. and Guzik, M.T.
Record Number:
6324
Year:
2023
Journal:
Environmental DNA
Pages:
1-14
Volume:
xx
Notes:
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited
Abstract:
Groundwater is an essential source of freshwater that supports surface ecosystems
as well as organisms adapted to living underground. The impacts of anthropogenic
climate change, extraction, and pollution pose major threats to groundwater ecosystem
health, prompting a need for efficient and reliable means to detect and monitor
subterranean faunal communities. Conventional survey of subterranean fauna relies
on the collection of organisms for morphological identification, which can be biased,
labor intensive, and often indeterminate at lower taxonomic levels. Environmental
DNA (eDNA)-based methods can dramatically improve on stygofaunal surveys, but
currently rely on time consuming active water filtration that limits the number of samples
that can be processed. Passive eDNA sampling, which involves submersion of
absorbent material (e.g. filter membrane, sponge etc.) into the sampled environment
for a fixed period, has shown promise as a viable alternative to active filtration in
aquatic ecosystems and may be applicable to groundwater systems. Here, we compared
groundwater eDNA collected from active pump filtered water samples, membranes
submerged in water for 10 min and 24 h, and haul-net samples morphologically
identified from bores at two geographically distinct locations in Western Australia.
Our results show that while the relative abundance of eDNA in groundwater (measured
through qPCR) is 100–800 times lower in passive samples, the species richness
detected is comparable between passive and active eDNA collection. Additionally,
standard metabarcoding assays (18S and COI) of passive eDNA samples detected
most subterranean orders identified morphologically (12/17), and this proportion may
be improved with increased sampling and application of DNA extraction methods that
increase DNA yield. Our findings demonstrate that passive eDNA sample collection is
a non-invasive survey method with the potential to improve the efficiency and replication
level of stygofaunal surveys but will benefit from further development.
Times Cited:
3