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The terrestrial subsurface hosts microbial communities that, collectively, are predicted to comprise as many microbial cells as global surface soils. Although initially thought to be associated with deposited organic matter, deep subsurface microbial communities are supported by chemolithoautotrophic primary production, with hydrogen serving as an important source of electrons. Despite recent progress, relatively little is known about the deep terrestrial subsurface compared to more commonly studied environments. Understanding the composition of deep terrestrial subsurface microbial communities and the factors that influence them is of importance because of human-associated activities including long-term storage of used nuclear fuel, carbon capture, and storage of hydrogen for use as an energy vector. In addition to identifying deep subsurface microorganisms, recent research focuses on identifying the roles of microorganisms in subsurface communities, as well as elucidating myriad interactions-syntrophic, episymbiotic, and viral-that occur among community members. In recent years, entirely new groups of microorganisms (i.e. candidate phyla radiation bacteria and Diapherotrites, Parvarchaeota, Aenigmarchaeota, Nanoloarchaeota, Nanoarchaeota archaea) have been discovered in deep terrestrial subsurface environments, suggesting that much remains unknown about this biosphere. This review explores the historical context for deep terrestrial subsurface microbial ecology and highlights recent discoveries that shape current ecological understanding of this poorly explored microbial habitat. Additionally, we highlight the need for multifaceted experimental approaches to observe phenomena such as cryptic cycles, complex interactions, and episymbiosis, which may not be apparent when using single approaches in isolation, but are nonetheless critical to advancing our understanding of this deep biosphere.
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http://dx.doi.org/10.1093/ismejo/wrae091 | DOI Listing |
Serpentinites, hydrated ultramafic rocks that produce [hyper]alkaline, reducing, H2-rich groundwaters, host subsurface microbial ecosystems. Though in the presence of enormous reducing power, life in serpentinizing systems is limited by oxidant and carbon availability. The forms of carbon that support the serpentinite-hosted microbiome, and their rates of biological assimilation, remain poorly understood.
View Article and Find Full Text PDFEnviron Monit Assess
August 2025
Centre for Climate Studies, Department of Civil Engineering, Manipal Institute of Technology, Manipal Academy of Higher Education, Manipal, Udupi, Karnataka, 576104, India.
Microplastic (MP) contamination in terrestrial ecosystems-particularly in agricultural soils-remains an underexplored environmental concern in India, an agriculture-driven economy. This study assessed MP contamination in paddy fields across 15 sites in Udupi (Karnataka) and Goa, with soil samples collected from the surface and at three subsurface depths (10, 20, and 30 cm). MPs were extracted using density separation, identified via stereomicroscopy and ATR-FTIR, and further characterized using SEM-EDS to examine surface morphology and elemental composition.
View Article and Find Full Text PDFAstrobiology
August 2025
International Centre for Terrestrial Antarctic Research, Te Whare Wānanga o Waikato-University of Waikato, Hamilton, New Zealand.
The McMurdo Dry Valleys may harbor diverse surface microbial communities, yet little is known about subsurface microorganisms in permafrost and their potential for paleoecological reconstruction. Here, we present microbial diversity and paleoecology from lower Wright Valley (7000- to 25,000-year-old) and Pearse Valley (>180,000-year-old) permafrost habitats in the McMurdo Dry Valleys. Using a new decontamination protocol, low-biomass extraction approaches, and 16S ribosomal RNA gene amplification sequencing, we assessed microbial community structure and diversity.
View Article and Find Full Text PDFmSystems
August 2025
School of Biological Sciences, The University of Auckland, Auckland, New Zealand.
Unlabelled: Bacterial genomes are highly dynamic entities, mostly due to horizontal gene transfer (HGT). HGT is thought to be the main driver of genetic variation and adaptation to the local environment in bacteria. However, little is known about the modalities of HGT within natural microbial communities, especially the implications of genetic exchange for streamlined microorganisms such as Patescibacteria (Candidate Phyla Radiation).
View Article and Find Full Text PDFEnviron Sci Technol
August 2025
Earth and Environmental Sciences Area, Lawrence Berkeley National Laboratory (LBNL), Berkeley, California 94720, United States.
The production, storage, and use of hydrogen are anticipated to grow substantially to achieve energy and climate goals. Consequently, microbial communities in many terrestrial and subsurface Earth environments could be exposed to elevated hydrogen concentrations. Hydrogen stimulates metabolic processes that reduce aqueous chemical species, such as bicarbonate or sulfate, that can exchange with solid mineral phases, but the controls on microbial hydrogenotrophy with mineral sources of electron acceptors are not fully understood.
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