Biogeochemical Cycles & Geobiology

Microbial Ecology Of Serpentinite-hosted Ecosystems

By Keith Cowing
Status Report
ISME via PubMed
April 8, 2025
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Microbial Ecology Of Serpentinite-hosted Ecosystems
Global distribution of serpentinization-influenced environments that have been investigated microbiologically and those that hosted 70 publicly available shotgun metagenomes used in the meta-analysis of this review. Geologic systems are indicated by points and abbreviations on the map, with those in green hosting metagenomes that were used in the meta-analysis of this review. Bottom left insert shows the pH distribution of water samples from which the metagenomes were derived, as reported by the original publication. Additional information for metagenomes is shown in Supplementary Table 1. Abbreviations are defined as follows (and further identified in Supplementary Table 1). NEY: Ney Springs; CED: The Cedars; CROMO: Coast Range Ophiolite Microbial Observatory; SEO: Santa Elena Ophiolite; TBL: Tablelands Ophiolite; RHF: Rainbow Hydrothermal Field; LCHF: Lost City Hydrothermal Field; LVF: Logatchev Vent Field; AVF: Ashadze Vent Field; AUR: Aurora Seamount; LEKA: Leka Ophiolite; CDV: Cabeço de Vide; VOL: Voltri Massif; YAN: Yanartaş; ALL: Allas Springs; SAM: Samail Ophiolite; KMR: Khalilovsky Massif; KHF: Karei Hydrothermal Field; OCHF: Old City Hydrothermal Field; HHS: Hakuba Happo Hot Springs; MAN: Manleluag Spring; LCR: La Crouen Spring; PBHF: Prony Bay Hydrothermal Field. — ISME via PubMed

Serpentinization, the collective set of geochemical reactions initiated by the hydration of ultramafic rock, has occurred throughout Earth history and is inferred to occur on several planets and moons in our solar system.

These reactions generate highly reducing conditions that can drive organic synthesis reactions potentially conducive to the emergence of life, while concomitantly generating fluids that challenge life owing to hyperalkalinity and limited inorganic carbon (and oxidant) availability.

Consequently, the serpentinite-hosted biosphere offers insights into the earliest life, the habitable limits for life, and the potential for life on other planets. However, the support of abundant microbial communities by serpentinites was only recognized ~20 years ago with the discovery of deep-sea hydrothermal vents emanating serpentinized fluids.

Here, we review the microbial ecology of both marine and continental serpentinization-influenced ecosystems in conjunction with a comparison of publicly available metagenomic sequence data from these communities to provide a global perspective of serpentinite microbial ecology. Synthesis of observations across global systems reveal consistent themes in the diversity, ecology, and functioning of communities. Nevertheless, individual systems exhibit nuances due to local geology, hydrology, and input of oxidized, near-surface/seawater fluids.

Further, several new (and old) questions remain including the provenance of carbon to support biomass synthesis, the physical and chemical limits of life in serpentinites, the mode and tempo of in situ evolution, and the extent that modern serpentinites serve as analogs for those on early Earth. These topics are explored from a microbial perspective to outline key knowledge-gaps for future research.

Microbial ecology of Serpentinite-hosted ecosystems, ISME via PubMed

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