2020
DOI: 10.1002/edn3.157
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Stirring up the relationship between quantified environmental DNA concentrations and exoskeleton‐shedding invertebrate densities

Abstract: This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Cited by 7 publications
(4 citation statements)
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“…There are also several knowledge gaps surrounding the use of eDNA within groundwaters, many of which involve the detection of crustacea, a dominant stygofauna taxa. Additional research on primers, the fate and transportation of DNA within aquifers and research on stygofauna DNA shedding capacity (Korbel, Rutlidge, et al, 2022; Trimbos et al, 2021) is required before this method can replace traditional sampling (Korbel, McKnight, et al, 2022; Saccò, Guzik, Van der Heyde, et al, 2022).…”
Section: Sampling Groundwater Faunamentioning
confidence: 99%
“…There are also several knowledge gaps surrounding the use of eDNA within groundwaters, many of which involve the detection of crustacea, a dominant stygofauna taxa. Additional research on primers, the fate and transportation of DNA within aquifers and research on stygofauna DNA shedding capacity (Korbel, Rutlidge, et al, 2022; Trimbos et al, 2021) is required before this method can replace traditional sampling (Korbel, McKnight, et al, 2022; Saccò, Guzik, Van der Heyde, et al, 2022).…”
Section: Sampling Groundwater Faunamentioning
confidence: 99%
“…Unlike the conventional quantitative PCR (qPCR), ddPCR has a higher reproducibility, is generally less sensitive to inhibitors, and does not require calibration curves or high replicate counts (Doi et al, 2015;Hindson et al, 2013;Nathan et al, 2014;Yang et al, 2014). The protocol for quantification of F:B ratio by ddPCR is inspired by work from Trimbos et al (2021) and is described in Appendix A. In addition to the ratio of fungal to bacterial DNA concentrations, the sum of both DNA concentrations was taken as a second indicator for total microbial abundance.…”
Section: Amendment Characterizationmentioning
confidence: 99%
“…Environmental DNA (eDNA) is a promising alternative to physical collection and processing [22][23][24]. The focus of species-specific crustacean eDNA assays using real-time quantitative polymerase chain reactions (rt-qPCR, henceforth qPCR) has often targeted rare or introduced species rather than abundant indicator species [25,26]. Water column eDNA may not allow for explicit crustacean quantification because much arthropod eDNA shedding may relate to molting processes that result in DNA deposition on or in the sediment [26][27][28].…”
Section: Introductionmentioning
confidence: 99%