Sedimentary archaeal amoA gene abundance reflects historic nutrient level and salinity fluctuations in Qinghai Lake, Tibetan Plateau

Sci Rep. 2015 Dec 15:5:18071. doi: 10.1038/srep18071.

Abstract

Integration of DNA derived from ancient phototrophs with their characteristic lipid biomarkers has been successfully employed to reconstruct paleoenvironmental conditions. However, it is poorly known that whether the DNA and lipids of microbial functional aerobes (such as ammonia-oxidizing archaea: AOA) can be used for reconstructing past environmental conditions. Here we identify and quantify the AOA amoA genes (encoding the alpha subunit of ammonia monooxygenases) preserved in a 5.8-m sediment core (spanning the last 18,500 years) from Qinghai Lake. Parallel analyses revealed that low amoA gene abundance corresponded to high total organic carbon (TOC) and salinity, while high amoA gene abundance corresponded to low TOC and salinity. In the Qinghai Lake region, TOC can serve as an indicator of paleo-productivity and paleo-precipitation, which is related to historic nutrient input and salinity. So our data suggest that temporal variation of AOA amoA gene abundance preserved in Qinghai Lake sediment may reflect the variations of nutrient level and salinity throughout the late Pleistocene and Holocene in the Qinghai Lake region.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ammonia
  • Archaea / classification
  • Archaea / enzymology
  • Archaea / genetics*
  • Archaeal Proteins / genetics*
  • Archaeal Proteins / metabolism
  • Carbon / metabolism
  • Ecosystem
  • Geography
  • Geologic Sediments / microbiology*
  • Lakes / chemistry
  • Lakes / microbiology*
  • Oxidoreductases / genetics*
  • Oxidoreductases / metabolism
  • Phylogeny
  • RNA, Archaeal / genetics
  • RNA, Ribosomal, 16S / genetics
  • Radiometric Dating / methods
  • Salinity
  • Tibet
  • Time Factors

Substances

  • Archaeal Proteins
  • RNA, Archaeal
  • RNA, Ribosomal, 16S
  • Carbon
  • Ammonia
  • Oxidoreductases
  • ammonia monooxygenase