Nitrous oxide (N 2 O) is the primary atmospheric constituent involved in stratospheric ozone depletion and contributes strongly to changes in the climate system through a positive radiative forcing mechanism. The atmospheric abundance of N 2 O has increased from 270 ppb (parts per billion, 10 −9 mole mole −1 ) during the pre-industrial era to approx. 330 ppb in 2018. Even though it is well known that microbial processes in agricultural and natural soils are the major N 2 O source, the contribution of specific soil processes is still uncertain. The relative abundance of N 2 O isotopocules ( 14 N 14 N 16 N, 14 N 15 N 16 O, 15 N 14 N 16 O, and 14 N 14 N 18 O) carries process-specific information and thus can be used to trace production and consumption pathways. While isotope ratio mass spectroscopy (IRMS) was traditionally used for high-precision measurement of the isotopic composition of N 2 O, quantum cascade laser absorption spectroscopy (QCLAS) has been put forward as a complementary technique with the potential for on-site analysis. In recent years, pre-concentration combined with QCLAS has been presented as a technique to resolve subtle changes in ambient N 2 O isotopic composition.From the end of May until the beginning of August 2016, we investigated N 2 O emissions from an intensively managed grassland at the study site Fendt in southern Germany. In total, 612 measurements of ambient N 2 O were taken by com-bining pre-concentration with QCLAS analyses, yielding δ 15 N α , δ 15 N β , δ 18 O, and N 2 O concentration with a temporal resolution of approximately 1 h and precisions of 0.46 ‰, 0.36 ‰, 0.59 ‰, and 1.24 ppb, respectively. Soil δ 15 N-NO − 3 values and concentrations of NO − 3 and NH + 4 were measured to further constrain possible N 2 O-emitting source processes. Furthermore, the concentration footprint area of measured N 2 O was determined with a Lagrangian particle dispersion model (FLEXPART-COSMO) using local wind and turbulence observations. These simulations indicated that nighttime concentration observations were largely sensitive to local fluxes. While bacterial denitrification and nitrifier denitrification were identified as the primary N 2 O-emitting processes, N 2 O reduction to N 2 largely dictated the isotopic composition of measured N 2 O. Fungal denitrification and nitrification-derived N 2 O accounted for 34 %-42 % of total N 2 O emissions and had a clear effect on the measured isotopic source signatures. This study presents the suitability of on-site N 2 O isotopocule analysis for disentangling source and sink processes in situ and found that at the Fendt site bacterial denitrification or nitrifier denitrification is the major source for N 2 O, while N 2 O reduction acted as a major sink for soil-produced N 2 O.