Nitrous oxide (N 2 O) is an increasing greenhouse gas in the troposphere and a potential destroyer of stratospheric ozone layer. Wastewater treatment plant (WWTP) is one of the anthropogenic N 2 O sources because inorganic and organic nitrogen compounds are converted to nitrate (NO 3 -, in the case of standard system) or N 2 (in the case of advanced system) by bacterial nitrification and denitrifcation processes in WWTP. These major processes can be distinguished by isotopocule analysis. In order to reveal production mechanisms of N 2 O in a standard wastewater treatment, we made water sampling at the central WWTP in Ulaanbaatar. The water samples collected from seven stations including biological reaction tanks were measured for concentration and isotopocule ratios of dissolved N 2 O and other inorganic nitrogen. Dissolved N 2 O concentration was extremely higher than that expected under atmospheric equilibrium (about 9 nmol/l) at all stations, indicating that this system is a potential source of N 2 O. It showed a gradual increase with the progress of biological reaction and the highest concentration (335.7 nmol/l) was observed at station N5-4 of the aeration tank when the DO was 5.7 mg/l. Nitrification by nitrifying bacteria could actively occur by the concentration of NH 4 + decreased whereas NO 2 -and NO 3 -showed a temporal and monotonic increase, respectively, under high DO concentration. Although the reported values of site preference (SP) of N 2 O, the difference in 15 N/ 14 N ratio between central (α) and terminal (β) nitrogen, produced via NO 2 -reduction (SP(ND)), including both nitrifier and denitrifier denitrification, and NH 2 OH oxidation (SP(HO)) ranged from -10.7‰ to 0‰ and 31.4‰ to 36.3‰, respectively, the observed SP at aeration tank was close to SP(ND) rather than SP(HO). It was ranged from 0.4‰ to 13.3‰ when N 2 O concentration was high, implying that the NO 2 -reduction made a greater contribution to N 2 O production. Slightly elevated SP (13.3‰) only at station N5-1 was derived from the mixing of N 2 O produced via NH 2 OH oxidation and the maximal contribution of this pathway was estimated to be about 40%. In other words, the contribution of NO 2 -reduction was more than 60%.