Nitrogen metabolism in different configuration design constructed wetlands under exposure of graphene oxide

Abstract

With occurrence of emerging contaminants in wastewater, nitrogen metabolism in constructed wetlands (CWs) should be re-evaluated at different environmental variables to withstand adversely exogenous contaminants. This study investigated functional gene, key enzyme, and microbe regulating nitrogen metabolism in three different configuration design CWs (planted W1 and W3 with full and low water level, unplanted W2 with full water level) when exposed to graphene oxide, one of most popular carbon-based nanomaterials. It was found that nitrogen removal was achieved by classical nitrification and denitrification, which was limited by nitrification in W2 and denitrification in planted CWs, presenting optimal balance between nitrification and denitrification in W1. Compared to W2, ammonium removals increased by 48% and 107% in W1 and W3, conversely total nitrogen removals decreased by 6% and 14% due to nitrate accumulation. Ammonia monooxygenase was the most sensitive to variables among four key enzymes. Bacteria were more abundant than archaea in CWs, both of functional genes and nitrifying populations were obviously affected by plant and water level in later period. The dominant denitrification populations were class Gammaproteobacteria followed by Alphaproteobacteria with the highest abundance observed in W2. Their species richness at genus level was higher on day 30 in W2 than planted CWs, but similar on day 120 in three CWs. The cooccurrence network and associated heatmap evidenced complex interaction among key enzymes, functional genes, and functional genera for nitrogen removal. KEGG annotations revealed specific differences in six core pathways of nitrogen metabolism in three CWs.