Although nitrogen (N) transformations have been widely studied under oxic or anoxic condition, few studies have been carried out to analyze the transformation accompanied with NO2--N accumulation. Particularly, the control… Click to show full abstract
Although nitrogen (N) transformations have been widely studied under oxic or anoxic condition, few studies have been carried out to analyze the transformation accompanied with NO2--N accumulation. Particularly, the control of mixed N species in N-transformation remains unclear in an oxic-anoxic transition zone (OATZ), a unique and ubiquitous redox environment. To bridge the gap, in this study, OATZ microcosms were simulated by surface water and sediments of a shallow lake. The N-transformation processes and rates at different NH4+-N/NO3--N ratios, and NO2--N accumulations in these processes were evaluated. N-transformation process exhibited a turning point. Simultaneous nitrification and denitrification occurred in its early stage (first 10 days, dissolved oxygen (DO) ≥ 2 mg/L) and then denitrification dominated (after 10 days, DO < 2 mg/L), which were not greatly affected by the NH4+-N/NO3--N ratio, on the contrary, the transformation rates of NH4+-N and NO3--N were distinctly affected. The NH4+-N transformation rates were positively correlated with the NH4+-N/NO3--N ratio. The highest NO3--N transformation rate was observed at an NH4+-N/NO3--N ratio of 1:1 with organic carbon/NO3--N of 3.09. The NO2--N accumulation, which increased with the decrease in NH4+-N/NO3--N ratio, was also controlled by organic carbon concentration and type. The peak concentration of NO2--N accumulation occurred only when the NO3--N transformation rate was particularly low. Thus, NO2--N accumulation may be reduced by adjusting the control parameters related to N and organic carbon sources, which enhances the theoretical insights for N-polluted aquatic ecosystem bioremediation.
               
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