Investigating sources and sinks of N 2 O expression from freshwater microbial communities in urban watershed sediments

Chemosphere. 2017 Dec;188:697-705. doi: 10.1016/j.chemosphere.2017.09.036. Epub 2017 Sep 11.

Abstract

Wastewater treatment plants (WWTPs) serve as point-source inputs for a variety of nutrients often dominated by nitrogenous compounds as a result of anthropogenic influence. These effluents can impact biogeochemical cycles in freshwater estuaries, influencing microbial communities in both the water and sediment compartments. To assess the impact of point source nutrients, a transect of sediment and pore water samples were collected from 4 locations in the Little River Sub-watershed including locations above and below the Little River Pollution Control Plant (LRPCP). Variation in chemistry and microbial community/gene expression revealed significant influences of the effluent discharge on the adjacent sediments. Phosphorus and sulfur showed high concentrations within plume sediments compared to the reference sediments while nitrate concentrations were low. Increased abundance of denitrifiers Dechloromonas, Dok59 and Thermomonas correlating with increased expression of nitrous-oxide reductase suggests a conversion of N2O to N2 within the LRPCP effluent sediments. This study provides valuable insight into the gene regulation of microbes involved in N metabolism (denitrification, nitrification, and nitrite reduction to ammonia) within the sediment compartment influenced by wastewater effluent.

Keywords: Metatranscriptomics; Microbial source tracking; Nitrogen cycling; Nutrient pollution; Sediment; Waste water treatment.

MeSH terms

  • Ammonia / analysis
  • Ammonia / metabolism
  • Denitrification*
  • Estuaries
  • Fresh Water / chemistry
  • Fresh Water / microbiology*
  • Gene Expression Regulation, Bacterial
  • Geologic Sediments / chemistry*
  • Geologic Sediments / microbiology
  • Nitrification*
  • Oxidoreductases / metabolism
  • Phosphorus / analysis
  • Sulfur / analysis
  • Waste Water / chemistry

Substances

  • Waste Water
  • Phosphorus
  • Sulfur
  • Ammonia
  • Oxidoreductases
  • nitrous oxide reductase