Differential efficiency of sampling devices in the measurement of microbial diversity of Yellowstone National Park hot springs

Abstract

Metagenomic characterization of low-biomass Yellowstone National Park (YNP) hot spring waters remains challenging because microbial recovery is influenced by filtration methodology, sample preservation, DNA extraction, and sequencing strategy. We characterized thermophilic microbial communities in alkaline YNP hot spring waters (62-90.5{degrees}C) using three high-temperature-compatible filtration systems (Sterivex, Supor, and polycarbonate membranes), automated onsite DNA extraction ({micro}Titan), and shotgun metagenomic sequencing with Illumina short-read and Oxford Nanopore Technologies (ONT) long-read platforms. Across all filtration systems and sequencing workflows, microbial communities were consistently dominated by Bacteria ([~]90% of reads), whereas Archaea represented 90% of recovered reads), whereas Archaea represented <10% of community abundance across all filtration systems. Although dominant microbial populations were reproducibly recovered, filtration-device selection influenced the recovery of microbial diversity and low-abundance taxa. By integrating field-deployable onsite DNA extraction with ONT shotgun metagenomic sequencing, this work evaluates practical workflows for studying thermophilic planktonic microbial communities under remote field conditions. These findings are relevant, not only to geothermal microbiology, but also to low-biomass environments in medical, pharmaceutical, and aerospace industries, where rapid onsite processing and contamination-aware workflows are essential for preserving authentic microbial signatures in extreme environments.