Evidence map›Paper›PMID 42016936›Full record

ArticleEcology and evolution2026

Optimizing a Novel eDNA-Based Framework for Reef Fish Biodiversity Monitoring Using an Autonomous Filtration System and in situ Nanopore Sequencing.

Lucie Cartairade, Julie Poulain, Quentin Carradec, Sophie Mangenot, Patrick Wincker, Serge Planes

Abstract read
In one paragraph

Article in Ecology and evolution, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Lucie CartairadeCNRS-EPHE-UPVD, UAR3278 CRIOBE PSL Research University Perpignan France.ORCID https://orcid.org/0009-0006-4185-2180
Julie PoulainGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS Univ Evry, Université Paris-Saclay France.ORCID https://orcid.org/0000-0002-8744-3116
Quentin CarradecGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS Univ Evry, Université Paris-Saclay France.ORCID https://orcid.org/0000-0003-4612-8678
Sophie MangenotGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS Univ Evry, Université Paris-Saclay France.ORCID https://orcid.org/0000-0002-6893-5502
Patrick WinckerGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS Univ Evry, Université Paris-Saclay France.ORCID https://orcid.org/0000-0001-7562-3454
Serge PlanesCNRS-EPHE-UPVD, UAR3278 CRIOBE PSL Research University Perpignan France.ORCID https://orcid.org/0000-0002-5689-5371

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Environmental DNA (eDNA) metabarcoding emerged as a powerful method for biodiversity monitoring, offering non-invasive, reproducible, and scalable assessments. However, its implementation in marine environments and remote regions still presents significant technical and logistical challenges. Here, we tested several methodologies to propose a comprehensive field-adapted eDNA metabarcoding workflow, from sampling to taxonomic analysis, designed for the specific challenge of fish biodiversity monitoring in coral reefs, but transferable to various aquatic ecosystems. We use large-volume water sampling using a custom-built autonomous underwater filtration system, which reduces contamination risks, simplifies logistics, and enhances sampling consistency. In this frame, we assess the efficiency of our custom underwater filtration system, different filter porosities, and water volumes to optimize DNA yield, showing that 20 L filtered on a 1.2 μm pore-size filter was optimal for collecting fish eDNA. We chose the mitochondrial 12S rRNA for DNA amplification then Oxford Nanopore Technologies sequencing for its portability and compatibility with tropical fieldwork. We developed a high-resolution 12S reference database encompassing around 400 fish sequences, representing over 50% of the known fish biodiversity in French Polynesia. Finally, we benchmark eDNA-based biodiversity data against traditional visual census observations across multiple reef habitats and temporal replicates. Our approach enables high-resolution monitoring both at spatial and temporal scales while providing a more comprehensive assessment of fish biodiversity richness compared to visual census methods. Diel sampling revealed pronounced temporal structure, with nocturnal taxa enriched at night. This study validates a fully integrated eDNA metabarcoding workflow, from field collection to taxonomic analysis, in diverse and remote marine ecosystems, providing a scalable and cost-efficient framework solution for long-term biodiversity monitoring in remote regions.

Indexed as

eDNAfish biodiversityFrench Polynesiametabarcodingnanopore

Identifiers

PMID42016936
PMCPMC13093698

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.