2022
DOI: 10.1002/edn3.342
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Evaluation of primer pairs for eDNA‐based assessment of Ephemeroptera, Plecoptera, and Trichoptera across a biogeographically diverse region

Abstract: Macroinvertebrates serve as key indicators in ecological assessments of aquatic ecosystems, where the composition and richness of their communities are indicative of environmental and anthropogenic change. Established monitoring of macroinvertebrates is expensive and time-consuming, and relies on expert taxonomic knowledge.In contrast, biomonitoring based on molecular tools can support faster characterization of aquatic communities but needs validation for the target taxonomic groups and the study region. Here… Show more

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Cited by 11 publications
(12 citation statements)
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References 53 publications
(90 reference statements)
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“…These results are congruent with the growing amount of comparisons between eDNA-based and traditional approaches ( 35 and references therein), showing that eDNA is not as efficient to detect rare macroinvertebrates as traditional sampling. Several reasons have been suggested to explain this discrepancy, either related to the nature of eDNA (e.g., shedding rates, DNA degradation), or to technical difficulties (e.g., primer bias, sequencing depth) (e.g., 36 , 37 ). In our case, however, two main factors possibly explain the observed differences.…”
Section: Discussionmentioning
confidence: 99%
“…These results are congruent with the growing amount of comparisons between eDNA-based and traditional approaches ( 35 and references therein), showing that eDNA is not as efficient to detect rare macroinvertebrates as traditional sampling. Several reasons have been suggested to explain this discrepancy, either related to the nature of eDNA (e.g., shedding rates, DNA degradation), or to technical difficulties (e.g., primer bias, sequencing depth) (e.g., 36 , 37 ). In our case, however, two main factors possibly explain the observed differences.…”
Section: Discussionmentioning
confidence: 99%
“…However, DNA fragments from these species are generally not well‐amplified by primers traditionally used in metabarcoding (e.g. Brantschen et al, 2022; Elbrecht & Leese, 2017; Leray et al, 2013). Thus, we modified the primers developed by Vamos et al (2017), amplifying a short fragment of the COI gene (205 bp), as follows: fwhF2_Niph 5′‐GGRTGAACAGTWTAYCCTCC‐3′ and fwhR2n_Niph 5′‐GTRATWGCTCCWGCTARMACTGG‐3′.…”
Section: Methodsmentioning
confidence: 99%
“…Samples were amplified using a 142 bp fragment of the COI marker, using the fwhF2 (Vamos et al, 2017) and EPTDr2n (Leese et al, 2021) primers with a modification that included Nextera® transposase sequences (see also Brantschen et al, 2022). Samples were randomly placed across four 96-well PCR plates.…”
Section: Molecular Analysesmentioning
confidence: 99%