ABSTRACT Field‐deployable DNA metabarcoding offers a transformative approach to biodiversity research and monitoring, yet its application remains limited due to technical constraints and a lack of reference data in poorly studied ecosystems. Combining isothermal Recombinase Polymerase Amplification (RPA) and Oxford Nanopore sequencing, we introduce a two‐step approach that uses non‐invasive species barcoding to directly generate reference sequences for use in environmental DNA (eDNA) metabarcoding, and enables real‐time, PCR‐free and cost‐effective molecular assessment of ecological communities in the field. Using an endemic and understudied tropical amphibian assemblage as a model, we demonstrate the functionality of this novel workflow. De novo generation of a reference sequence library from amphibian skin swab samples significantly improved the accuracy and taxonomic resolution of sequence assignments from eDNA samples, particularly on the species level, in turn allowing a characterisation of fine‐scale patterns in community composition. Beyond generating new RPA‐compatible amphibian metabarcoding primers, our results show that combining field‐based eDNA metabarcoding with the offline assembly of a local reference database can directly bridge existing data gaps in molecular biodiversity monitoring, providing a scalable solution to accelerate biodiversity assessments in data‐deficient ecosystems. This workflow paves the way for broader deployment of molecular tools in global biodiversity hotspots—particularly in remote and resource‐limited tropical regions—to directly contribute critical baseline data, and support conservation efforts in regions where they are most urgently needed.
Erens et al. (Tue,) studied this question.