Diverse Thaumarchaeota Dominate Subsurface Ammonia-oxidizing Communities in Semi-arid Floodplains in the Western United States

Microb Ecol. 2020 Nov;80(4):778-792. doi: 10.1007/s00248-020-01534-5. Epub 2020 Jun 13.

Abstract

Subsurface microbial communities mediate biogeochemical transformations that drive both local and ecosystem-level cycling of essential elements, including nitrogen. However, their study has been largely limited to the deep ocean, terrestrial mines, caves, and topsoils (< 30 cm). Here, we present regional insights into the microbial ecology of aerobic ammonia oxidation within the terrestrial subsurface of five semi-arid riparian sites spanning a 900-km N-S transect. We sampled sediments, profiled communities to depths of ≤ 10 m, and compared them to reveal trends regionally within and surrounding the Upper Colorado River Basin (CRB). The diversity and abundance of ammonia-oxidizing microbial communities were evaluated in the context of subsurface geochemistry by applying a combination of amoA (encoding ammonia monooxygenase subunit A) gene sequencing, quantitative PCR, and geochemical techniques. Analysis of 898 amoA sequences from ammonia-oxidizing archaea (AOA) and bacteria (AOB) revealed extensive ecosystem-scale diversity, including archaeal amoA sequences from four of the five major AOA lineages currently found worldwide as well as distinct AOA ecotypes associated with naturally reduced zones (NRZs) and hydrogeochemical zones (unsaturated, capillary fringe, and saturated). Overall, AOA outnumber AOB by 2- to 5000-fold over this regional scale, suggesting that AOA may play a prominent biogeochemical role in nitrification within terrestrial subsurface sediments.

Keywords: Ammonia-oxidizing archaea; Ammonia-oxidizing bacteria; Nitrification; Terrestrial subsurface; Thaumarchaeota; amoA.

MeSH terms

  • Ammonia / metabolism*
  • Archaea / isolation & purification
  • Archaea / physiology*
  • Colorado
  • Ecosystem
  • Floods
  • Microbiota / physiology*
  • New Mexico
  • Oxidation-Reduction
  • Soil Microbiology*
  • Wyoming

Substances

  • Ammonia